US3313007A - Method of making sheet metal forming dies - Google Patents
Method of making sheet metal forming dies Download PDFInfo
- Publication number
- US3313007A US3313007A US303783A US30378363A US3313007A US 3313007 A US3313007 A US 3313007A US 303783 A US303783 A US 303783A US 30378363 A US30378363 A US 30378363A US 3313007 A US3313007 A US 3313007A
- Authority
- US
- United States
- Prior art keywords
- mold
- cavity
- die
- shot
- particles
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 229910052751 metal Inorganic materials 0.000 title description 59
- 239000002184 metal Substances 0.000 title description 59
- 238000004519 manufacturing process Methods 0.000 title description 7
- 238000000034 method Methods 0.000 claims description 88
- 239000002245 particle Substances 0.000 claims description 66
- 229910045601 alloy Inorganic materials 0.000 claims description 55
- 239000000956 alloy Substances 0.000 claims description 55
- 238000005219 brazing Methods 0.000 claims description 49
- 239000000919 ceramic Substances 0.000 claims description 29
- 239000000945 filler Substances 0.000 claims description 29
- 238000010438 heat treatment Methods 0.000 claims description 20
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 18
- XFWJKVMFIVXPKK-UHFFFAOYSA-N calcium;oxido(oxo)alumane Chemical compound [Ca+2].[O-][Al]=O.[O-][Al]=O XFWJKVMFIVXPKK-UHFFFAOYSA-N 0.000 claims description 18
- 229910052664 nepheline Inorganic materials 0.000 claims description 18
- 239000010434 nepheline Substances 0.000 claims description 18
- 239000010435 syenite Substances 0.000 claims description 18
- 239000001257 hydrogen Substances 0.000 claims description 17
- 229910052739 hydrogen Inorganic materials 0.000 claims description 17
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical class [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 15
- 239000004576 sand Substances 0.000 claims description 15
- 238000003754 machining Methods 0.000 claims description 14
- 238000001816 cooling Methods 0.000 claims description 10
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 8
- 238000002844 melting Methods 0.000 claims description 8
- 230000008018 melting Effects 0.000 claims description 8
- 229910052725 zinc Inorganic materials 0.000 claims description 8
- 239000011701 zinc Substances 0.000 claims description 8
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 7
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 7
- 229910052802 copper Inorganic materials 0.000 claims description 7
- 239000010949 copper Substances 0.000 claims description 7
- 230000003647 oxidation Effects 0.000 claims description 7
- 238000007254 oxidation reaction Methods 0.000 claims description 7
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 6
- 229910044991 metal oxide Inorganic materials 0.000 claims description 6
- 150000004706 metal oxides Chemical class 0.000 claims description 6
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 claims description 5
- 229910052757 nitrogen Inorganic materials 0.000 claims description 4
- 229910052782 aluminium Inorganic materials 0.000 claims description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 3
- 229910052787 antimony Inorganic materials 0.000 claims description 3
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 claims description 3
- 230000003247 decreasing effect Effects 0.000 claims description 3
- 229910052759 nickel Inorganic materials 0.000 claims description 3
- 229910052710 silicon Inorganic materials 0.000 claims description 3
- 239000010703 silicon Substances 0.000 claims description 3
- 239000000203 mixture Substances 0.000 description 67
- 230000008569 process Effects 0.000 description 66
- 239000010959 steel Substances 0.000 description 45
- 229910000831 Steel Inorganic materials 0.000 description 42
- 239000007789 gas Substances 0.000 description 38
- 238000005266 casting Methods 0.000 description 34
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 17
- 239000000463 material Substances 0.000 description 16
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 16
- 239000004115 Sodium Silicate Substances 0.000 description 15
- 229910052911 sodium silicate Inorganic materials 0.000 description 15
- 229910001018 Cast iron Inorganic materials 0.000 description 9
- 239000003345 natural gas Substances 0.000 description 8
- 230000008901 benefit Effects 0.000 description 7
- 230000002829 reductive effect Effects 0.000 description 7
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 6
- 238000005524 ceramic coating Methods 0.000 description 6
- -1 sodium aluminum silicates Chemical class 0.000 description 6
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 5
- 229910001208 Crucible steel Inorganic materials 0.000 description 5
- 230000009471 action Effects 0.000 description 5
- 238000005495 investment casting Methods 0.000 description 5
- 239000000843 powder Substances 0.000 description 5
- 238000007711 solidification Methods 0.000 description 5
- 230000008023 solidification Effects 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 239000011230 binding agent Substances 0.000 description 4
- 238000005336 cracking Methods 0.000 description 4
- 239000002923 metal particle Substances 0.000 description 4
- 239000005995 Aluminium silicate Substances 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 3
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 3
- 235000012211 aluminium silicate Nutrition 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 229910052742 iron Inorganic materials 0.000 description 3
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 3
- 239000010450 olivine Substances 0.000 description 3
- 229910052609 olivine Inorganic materials 0.000 description 3
- 239000011505 plaster Substances 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 239000004698 Polyethylene Substances 0.000 description 2
- 229910000653 SAE 1095 Inorganic materials 0.000 description 2
- 229910021529 ammonia Inorganic materials 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 229910052793 cadmium Inorganic materials 0.000 description 2
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 2
- 239000004568 cement Substances 0.000 description 2
- 229910010293 ceramic material Inorganic materials 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 230000001447 compensatory effect Effects 0.000 description 2
- 238000009792 diffusion process Methods 0.000 description 2
- 235000013312 flour Nutrition 0.000 description 2
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 description 2
- 229910010272 inorganic material Inorganic materials 0.000 description 2
- 239000011147 inorganic material Substances 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 230000001788 irregular Effects 0.000 description 2
- 239000000395 magnesium oxide Substances 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 235000010755 mineral Nutrition 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 235000019353 potassium silicate Nutrition 0.000 description 2
- 239000011253 protective coating Substances 0.000 description 2
- 230000001681 protective effect Effects 0.000 description 2
- 241000870659 Crassula perfoliata var. minor Species 0.000 description 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- 229910001315 Tool steel Inorganic materials 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 229910052656 albite Inorganic materials 0.000 description 1
- 238000005275 alloying Methods 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 239000010425 asbestos Substances 0.000 description 1
- 229910052626 biotite Inorganic materials 0.000 description 1
- 229910052810 boron oxide Inorganic materials 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000004891 communication Methods 0.000 description 1
- 230000002860 competitive effect Effects 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 230000008602 contraction Effects 0.000 description 1
- JKWMSGQKBLHBQQ-UHFFFAOYSA-N diboron trioxide Chemical compound O=BOB=O JKWMSGQKBLHBQQ-UHFFFAOYSA-N 0.000 description 1
- YGANSGVIUGARFR-UHFFFAOYSA-N dipotassium dioxosilane oxo(oxoalumanyloxy)alumane oxygen(2-) Chemical compound [O--].[K+].[K+].O=[Si]=O.O=[Al]O[Al]=O YGANSGVIUGARFR-UHFFFAOYSA-N 0.000 description 1
- UQGFMSUEHSUPRD-UHFFFAOYSA-N disodium;3,7-dioxido-2,4,6,8,9-pentaoxa-1,3,5,7-tetraborabicyclo[3.3.1]nonane Chemical compound [Na+].[Na+].O1B([O-])OB2OB([O-])OB1O2 UQGFMSUEHSUPRD-UHFFFAOYSA-N 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 239000002360 explosive Substances 0.000 description 1
- 230000004907 flux Effects 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- SZVJSHCCFOBDDC-UHFFFAOYSA-N iron(II,III) oxide Inorganic materials O=[Fe]O[Fe]O[Fe]=O SZVJSHCCFOBDDC-UHFFFAOYSA-N 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- 238000005058 metal casting Methods 0.000 description 1
- 239000007769 metal material Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 229910052651 microcline Inorganic materials 0.000 description 1
- 239000006082 mold release agent Substances 0.000 description 1
- 229910052627 muscovite Inorganic materials 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen(.) Chemical compound [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000002985 plastic film Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000000750 progressive effect Effects 0.000 description 1
- 238000005086 pumping Methods 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 229910052895 riebeckite Inorganic materials 0.000 description 1
- 238000007790 scraping Methods 0.000 description 1
- 239000003566 sealing material Substances 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- KKCBUQHMOMHUOY-UHFFFAOYSA-N sodium oxide Chemical compound [O-2].[Na+].[Na+] KKCBUQHMOMHUOY-UHFFFAOYSA-N 0.000 description 1
- 229910001948 sodium oxide Inorganic materials 0.000 description 1
- 235000019794 sodium silicate Nutrition 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 230000008016 vaporization Effects 0.000 description 1
- 238000013022 venting Methods 0.000 description 1
- 239000007966 viscous suspension Substances 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Images
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B23—MACHINE TOOLS; METAL-WORKING NOT OTHERWISE PROVIDED FOR
- B23K—SOLDERING OR UNSOLDERING; WELDING; CLADDING OR PLATING BY SOLDERING OR WELDING; CUTTING BY APPLYING HEAT LOCALLY, e.g. FLAME CUTTING; WORKING BY LASER BEAM
- B23K35/00—Rods, electrodes, materials, or media, for use in soldering, welding, or cutting
- B23K35/22—Rods, electrodes, materials, or media, for use in soldering, welding, or cutting characterised by the composition or nature of the material
- B23K35/24—Selection of soldering or welding materials proper
- B23K35/30—Selection of soldering or welding materials proper with the principal constituent melting at less than 1550 degrees C
- B23K35/302—Cu as the principal constituent
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B21—MECHANICAL METAL-WORKING WITHOUT ESSENTIALLY REMOVING MATERIAL; PUNCHING METAL
- B21D—WORKING OR PROCESSING OF SHEET METAL OR METAL TUBES, RODS OR PROFILES WITHOUT ESSENTIALLY REMOVING MATERIAL; PUNCHING METAL
- B21D37/00—Tools as parts of machines covered by this subclass
- B21D37/20—Making tools by operations not covered by a single other subclass
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22C—FOUNDRY MOULDING
- B22C1/00—Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds
- B22C1/16—Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds characterised by the use of binding agents; Mixtures of binding agents
- B22C1/18—Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds characterised by the use of binding agents; Mixtures of binding agents of inorganic agents
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22C—FOUNDRY MOULDING
- B22C9/00—Moulds or cores; Moulding processes
- B22C9/06—Permanent moulds for shaped castings
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S428/00—Stock material or miscellaneous articles
- Y10S428/922—Static electricity metal bleed-off metallic stock
- Y10S428/9335—Product by special process
- Y10S428/939—Molten or fused coating
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/12—All metal or with adjacent metals
- Y10T428/12014—All metal or with adjacent metals having metal particles
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/12—All metal or with adjacent metals
- Y10T428/12014—All metal or with adjacent metals having metal particles
- Y10T428/1216—Continuous interengaged phases of plural metals, or oriented fiber containing
Definitions
- This invention relates generally to casting metal ar ticles. More particularly, this invention relates to precision cast-to-size brazed shot dies and to a method of making same.
- Most commonly used casting techniques for casting metal articles involve the step of pouring molten metal, such as cast iron or steel, into a mold cavity which is contoured to the general size and shape of the article to be produced.
- molten metal such as cast iron or steel
- Molds made of sand or similar ceramic materials are widely used in metal casting processes, since ceramic molds are relatively inexpensive and easy to fabricate.
- Most commonly used ceramic molds have fairly good structural strength at the relatively high temperatures employed in most commonly used iron or steel casting processes, and also they are relatively resistant to the diffusion of the molten metal into the Walls of the mold cavity during the casting process.
- casting processes in which metal articles such as cast iron or steel dies are cast in ceramic molds, usually involve problems of size and shape control in forming the article, since the articles which are formed by these processes generally have a somewhat different size and shape than the initial size and shape of the mold cavity.
- the problem of controlling the final size and shape of the metal article, such as a steel or cast iron die, formed by most commonly used casting processes generally is attributed to the difference in the characteristics of thermal expansion of the ceramic mold and the characteristics of thermal and solidification shrinkage of the metallic die.
- thermal expansion characteristics of the mold We refer to the manner in which the mold cavity becomes enlarged and deformed from its initial size and shape on being heated during the casting process.
- thermal shrinkage characteristics of the metallic die we refer to the manner in which the molten metal materials in the mold cavity solidify and contract on cooling to form the die.
- thermal shrinkage characteristics shrinkage due to solidification as well as thermal contraction is included in the term thermal shrinkage characteristics.
- thermal expansion characteristics of a ceramic mold usually differ from the thermal shrinkage characteristics of a metallic casting
- metal dies which are made by a casting technique utilizing ceramic molds generally have a different size and shape than the initial size and shape of the mold cavity.
- differential solidification rates between the heavy and light sections of the castings usually cause a considerable amount of distortion. In fact, this latter problem is often the major cause of distortion in casting a metal article or die.
- precision cast-to-size dies we refer to dies which are formed by a casting process in which the cast die has substantially the same size and shape as the initial size and shape of the mold cavity.
- this type of precision casting process offers by eliminating or greatly reducing the number of necessary post-machining op erations, it also offers other process advantages. For instance, such a process eliminates the necessity of forming an enlarged mold cavity and permits the direct use of the die pattern or master model, which are exact duplicates of the die to be produced, to form the mold cavity.
- the die which is produced in the mold cavity will have substantially the same size and shape as the master model or die pattern used to form the mold cavity.
- the present invention involves a precision casting process utilizing a brazing procedure to form metal articles, such as brazed shot dies.
- metal articles such as brazed shot dies.
- the brazed shot dies so produced generally have excellent wear resistance which in many cases is superior to com monly used dies which are cast from steel or cast iron.
- the process of the present invention by which small metal shot particles are brazed together to form brazed shot dies, substantially eliminates the problems of solidification shrinkage previously mentioned in the case of casting irregular shaped metal articles having heavy and light sections.
- brazing techniques used in making metal articles similar to the brazed shot dies of the present invention generally involve the use of more expensive process steps, equipment and materials than the processes, equipment and materials used in most commonly used casting processes to cast metal articles, such as cast steel or cast iron dies.
- brazing techniques often require the use of expensive furnace equipment having a special protective furnace atmosphere to prevent oxidation of the brazing alloy or metal parts which are being brazed together.
- the brazing alloys and metal shot and filler particles used to form the brazed shot dies of the present invention are generally more expensive materials for use in forming a die than regular tool steel or cast iron.
- brazed shot dies Accordingly, the reduction in post-machining costs realized by using a precision casting process to form brazed shot dies would make the use of these dies economically competitive in most applications with the use of cast steel or cast iron dies which are made by most commonly used casting processes and which require substantial postmachining operations.
- the superior wear resistance and long life of brazed shot dies offer additional operational advantages over the use of dies cast from steel or cast iron in many applications, such as sheet metal forming processes.
- a process for making precision cast-to-size brazed shot dies has not heretofore been recognized.
- the process of making the precision cast-to-size brazed shot dies of the present invention involves the steps of providing a master model having the exact size and shape of the die which is to be produced, positioning the model in a suitable mold assembly, pouring a suitably mixed mold composition into the mold assembly over the model, curing the mold composition to form a ceramic mold and subsequently removing the cured mold from the mold assembly and the model from the mold to provide the mold cavity.
- Metal shot and metal filler particles are next placed in the mold cavity in the desired arrangement, and the mold is placed in a suitable furnace and heated in a suitable protective atmosphere to a suitable temperature level above the pouring temperature of the brazing alloy which is to be used.
- a molten brazing alloy is poured into the mold cavity over the heated shot and fillter particles to fill the voids therebetween, and the ceramic mold and metal composition in the mold cavity are subsequently cooled in the furnace so that the alloy solidifies and brazcs the metal shot and metal particles together to form the brazed shot die embodying the present invention.
- the die compositions of the present invention solidify and contract, thereby shrinking to the same extent as the mold cavity expands on heating, so that the brazed shot die which is formed has substantially the same size and shape as the initial shape of the mold cavity when the model is removed.
- the precision cast-to-size brazed shot die is subsequently removed from the mold cavity. Since the die which is formed by the process of the present invention has substantially the same size and shape as the model used to form the mold cavity, the number and extent of post-machining and handling operations necessary to conform the die to the desired final shape is greatly reduced.
- FIGURE 1 is a perspective view, with parts broken away, of a mold assembly which may be used to form the mold embodying the present invention
- FIGURE 2 is a vertical clevational view, with parts broken away and in section, of a furnace assembly and appurtenances which may be used in accordance with the proce s of the present invention to make the precision cast-to-size brazed shot dies of the present invention;
- FlGURE 3 is a vertical elevational view, with parts broken away and in section, of a precision cast-to-size brazed shot die embodying the present invention.
- FIGURE 1 of the drawing a typical mold assembly is illustrated which may be used to form the ceramic mold embodying the present invention.
- Four rectanguiar, plate-like wall members I! are vertically mounted on a fiat, rectangular base member 12 to form a cubical mold cavity 14 which opens upwards.
- the wall members and the base member may be made of wood or any other suitable material. These members may be detachably but firmly secured to one another by any suitable means, such as dowel pins, which are not shown in the drawing.
- the precision casting process of the present invention permits the direct use of a duplicate model of the die to be produced, since the necessity of casting an oversize die is eliminated. Naturally, this is an important advantage of the present invention.
- the model may be made of plaster or any other suitable material, such as plastic.
- the upper contoured surface 13 of the model preferably is treated in a conventional manner with any suitable parting agent or mold release agent.
- any suitable parting agent or mold release agent such as a silicone oil, to facilitate removal of the model after the mold has been formed.
- a parting agent which is commercially marketed under the trade name Aristo No. 5950" is suitable for use with a plaster model and the ceramic mold compositions of the present invention.
- the present invention con templates the use of mold compositions having thermal expansion characteristics which are substantially equal to the thermal shrinkage characteristics of the brazed shot die compositions of the present invention, so that the aforementioned problems of size and shape control, which arise due to dilferences in these characteristics, are greatly reduced or eliminated.
- a mold comprising, on a weight basis, about to nepheline syenite sand as the base material with about 3% to 10% sodium silicate and 2% to 10% calcium aluminate as binders
- the mold has a composition, by weight, of about 84% to 91% nepheline syenite, about 5% to 8% calcium aluminate and about 4% to 8% sodium silicate.
- Nepheline syenite is a commercially available ceramic material which consists essentially of a mixture of several different sodium aluminum silicates and potassium aluminum silicates.
- a typical analysis of nepheline syenite on a volumetric percent basis which is suitable for use in the process of the present invention is listed in Table I below:
- nepheline syenite volume Albite 54 Microcline 20 Nepheline 2O Muscovite 2 Mafics 2 Balance (Biotite, Hastingsite, Magnetite) 2 Total "W0
- nepheline syenite having a mesh size ranging from 20 to 40 mesh.
- the mesh size and the mineral composition of the nepheline syenite may be varied somewhat from the composition listed in Table I and the mesh size specified in the preferred embodiment of the invention.
- an aqueous solution of sodium silicate or waterglass and calcium aluminate are used conjointly to bind the ceramic mold compositions used in the process of the present invention.
- a viscous, aqueous solution of sodium silicate having an Na O content ranging, by weight, from about 14.8% to 15.2% and SiO content ranging, by weight, from about 28% to 29% with the balance being water.
- the calcium aluminate cement which is used preferably is in the form of a finely divided powder having a mesh size of less than 100 mesh.
- the sodium silicate and the calcium aluminate binders are mixed in a suitable mulling apparatus with the nepheline syenite sand.
- the nepheline syenite sand and cal cium aluminate powder are added to the mulling machine and mulled for about 1 /2 to 3 minutes to thoroughly mix the powders.
- the sodium silicate solution preferably is next slowly added to the powdered mixture and mulled for about 2 to 3 minutes until a moist, sandy mass is formed.
- the ceramic mixture is subsequently poured into the cavity 14 of the mold assembly to form the mold 22.
- the mixture is most advantageously added in small separate portions with each portion being firmly packed in the cavity by using any suitable device, such as a pneumatic rammer, until the last portion is added and packed so that the cavity 14 is completely filled.
- the progressive packing after each portion of the ceramic mixture is added serves to eliminate voids in the cavity of the mold assembly.
- the thickness of the ceramic mixture between the walls of the mold assembly and the model 16 preferably ranges from about 6 inches to 12 inches
- the thickness of the mold between the top of the cavity and the model preferably ranges from about 2%. inches to 6 inches to minimize the temperature gradient across the mold walls, thereby preventing cracking of the mold during the die forming process.
- the excess sand at the top of the cavity 14 preferably is leveled off with the top surface of the cavity walls 10 by any suitable means, such as by scraping the excess sand off with a straight edge.
- a shallow cylindrical opening 24 and a plurality of shallow elongated grooves 26, which extend radially from the opening, may be formed in the leveled top surface 28 of the mold 22 directly above the model 16 in the cavity 1.4.
- the opening and grooves facilitate the heating of the mold and the die composition when large dies are being cast by providing a path for the distribution of the furnace atmosphere gas through the die compostion and walls of the mold cavity during the heating cycle 'of the casting process, which will hereinafter be more fully described.
- smaller dies or castings which are made using smaller molds do not necessarily require gas flow through them, except to reduce the moisture content 'of the mold.
- an asbestos rope seal 30 or similar sealing material which can withstand high temperatures, preferably is positioned in a groove provided in the top surface 28 of the mold 22 surrounding the opening 24 and the grooves 26.
- the seal 30 serves to prevent the furnace atmosphere gas from being drawn from the furnace between the top surface 28 of the ceramic mold and the rectangular metal base plate 32 which is used to support the mold in the furnace during the heating cycle of the casting process.
- the metal base plate 32 may be made of steel or other suitable material which is capable of withstanding the high temperatures employed in the furnace.
- the base plate 32 may be aflixed to the top of the mold assembly by any suitable means, such as tie studs, 34, which extend from the top surface of the walls 10 of the mold assembly into openings 36 provided in the base plate.
- the base plate is positioned so that a flush fit is obtained between the plate and the leveled top surface of the sand mixture.
- the base plate 32 also is provided with a cylindrical opening 38 which extends through the top and bottom surfaces of the plate so that it is coaxially aligned and in communication with the cylindrical opening 24 in the top surface 28 of the sand mixture. As previously mentioned, hot furnace atmosphere gas is drawn through this opening during the casting process.
- the surface of the base plate which contacts the mixture preferably is treated with a protective coating to prevent oxidation of the base plate and sticking of the mold to the base plate during the casting process.
- a suitable ceramic coating for this purpose is commercially marketed under the trade name of Fiberfrax QF180.
- This material is a viscous suspension of finely divided, powdered inorganic materials in water and has a total solids content of about 69%. by weight.
- the total solids content of the material consists essentially, by weight, of about 57% silicon dioxide, about 41% alumina and the balance including small quantities of sodium oxide, boron oxide, magnesium oxide and traces of other inorganic materials.
- the mold assembly may be inverted by any suitable means so that the ceramic mixture rests firmly on the metal base plate 32.
- the mixture preferably is allowed to cure at room temperature for an initial curing period of about 1 to 2 hours with the mold assembly in place.
- the mixture is substantially cured during this initial curing period and forms a relatively firm mold.
- the wooden members of the mold assembly and the pattern or model 16 are removed by any suitable means.
- the mold is covered with a plastic sheet, such as polyethylene, and allowed to stand for about 48 hours to complete the cure.
- the polyethylene sheet serves to retain moisture in the mold, thereby aiding the formation of chemical bonds which harden the mold during the mold curing cycle.
- the chemical reactions which take place during the curing cycle between the calcium aluminate and the sodium silicate binders and the nepheline syenite sand base are very complex and not too Well understood. However, it is believed that the calcium aluminate causes the so dium silicate to set up and form alkaline earth metalsodium silicate bonds in the ceramic mixture.
- the cured mold thus formed has excellent strength and high resistance to cracking when used in the process of the present invention to form the precision cast-to-size brazed slot dies of the present invention.
- the outer side walls and top surfaces of the mold preferably are treated with a suitable heat-resistant ceramic coating to make these surfaces substantially impervious to the passage of the furnace atmosphere gas from the furnace through these surfaces during the heating cycle of the casting process.
- the upper wall portion of the mold cavity also preferably is treated with a ceramic coating.
- the lower face portion of the mold cavity preferably is not treated so that the furnace atmosphere gas may pass through this portion of the mold cavity during the heating cycle of the casting process, as will hereinafter be more fully described.
- a ceramic coating material consisting. by weight, of about 17% olivine Hour, kaolin powder and about 58% sodium silicate.
- the olivine flour preferably has a mesh size ranging from 180 mesh to about 220 mesh.
- the kaolin powder preferably has a mesh size of less than 350 mesh.
- the sodium silicate used in the coating preferably has the same composition as the previously mentioned sodium silicate composition used in forming the mold.
- other ceramic coating materials may be used to coat the mold surfaces for the above-mentioned purposes in accordance with the process of the present invention.
- the ceramic coating mixture in the preferred embodiment of the present invention may be prepared by mixing the ingredients in any suitable mixing apparatus until a viscous mixture is formed. The mixture is then applied to the above-mentioned mold surfaces by any suitable means, such as a paint brush, until these surfaces are substantially impregnated with the coating and are relatively impervious. In this manner, the flow of furance atmosphere gas through the mold during the heating cycle of the die making process is substantially confined to a path through the bottom surface of the mold cavity and the opening 24 in the bottom of said mold. Also, we have found that this coating increases the strength of the mold against cracking.
- FIGURE 2 of the drawing illustrates the method by which the precision cast-to-size brazed shot dies of the present invention are made.
- the cured ceramic mold 22 is positioned on the metal base plate 32 with the mold cavity 39 opening upwards.
- the base plate is suitably mounted on pedestals 40 within an enclosed furance 42 which may be heated by any suitable means, not shown in the drawing.
- the brazed shot die compositions of the present invention have compensatory thermal shrinkage characteristics relative to the thermal expansion characteristics of the mold compositions of the present invention.
- relatively small metal shot particles and relatively large metal filler particles In casting relatively large dies by the precision casting process of the present invention, we contemplate the use of relatively small metal shot particles and relatively large metal filler particles.
- the metal filler particles may be omitted from the die composition.
- the shot and balls may be made of any suitable steel, such as SAE 1095 steel, or other suitable metal.
- SAE 1095 steel or other suitable metal.
- the size, shape and composition of the shot and filler particles is not limited to the size, shape and composition of the shot and filler particles of the preferred embodiment of the invention. In other words, these characteristics of the shot and filler particles may be varied if corresponding changes are made in the mold composition so that the thermal shrinkage characteristics of the die composition are compensatory relative to the thermal expansion characteristics of the mold in accordance with the process of the present invention.
- the shot is sufficiently small so that capillary action occurs when the molten brazing alloy is poured into the mold cavity to braze the shot and particles together, as will hereinafter be more fully explained.
- a typical analysis of steel shot used in the preferred embodiment of the present invention is listed in Table III below:
- the shot and balls Prior to placing the shot and balls in the mold cavity, they preferably are thoroughly cleaned by any suitable means to remove dust and other impurities which may interfere with the brazing process.
- any suitable means to remove dust and other impurities which may interfere with the brazing process.
- the process of the present invention used to form a sheet metal forming die, and since the brazed shot material has superior qualities as a draw die surface than the relatively large filler particles, it is desirable to keep the filler material away from the working surface of the die which is made for such an application.
- a portion of shot may be added to the mold cavity 39 to cover the lower face 43 of the cavity when the die is to be used in a sheet metal forming press assembly.
- the layer of shot 42 so added preferably ranges in thickness from about /2 inch to about 1 /2 inches. Another advantage of providing this layer of small diameter shot on the lower portion of the die is that it facilitates the machining and finishing of the die after the casting process is completed.
- the steel ball filler particles is poured into the mold cavity over the layer of shot to fill a part of the upper portion 44 of the mold cavity. Subsequently, a portion of the small diameter shot is also added to the upper portion of the cavity to fill the voids between the balls.
- the steel balls and shot most advantageously are poured into the cavity in successive alternate layers until the cavity is filled.
- the shot and balls may be vibrated after each addition by any suitable means to insure that they are tightly packed in the mold cavity.
- the balls also are a relatively cheap filler material and substantially reduce the cost of producing the larger sized brazed shot dies of the present invention.
- Thermocouples 46 preferably are inserted in the mold cavity and the mold body in any suitable manner to measure the temperature of the mold and the die compositions during the die forming process.
- the thermocouples may be of any suitable type which will give relatively accurate temperature readings in the relatively high temperature ranges employed in the die forming process.
- the thermocouples may be connected by lead wires 48 to an instrument box 50 located outside of the furnace so that temperature readings of the die composition and the mold may be recorded during the die forming process.
- the brazed shot die which is formed by the process illustrated in FIGURE 2 is typical of a punch portion of a sheet metal forming die.
- a punch die When a punch die is used in a sheet metal press assembly, it is usually afiixed to a movable member in the sheet metal press assembly by Welding or mechanically locking the die to the member.
- an extension member for positioning the die in a sheet metal press assembly may be partially embedded in the shot and balls in the mold cavity so that when the die is cast the extension member and the die are formed into an integral punch unit.
- FIGURE 2 of the drawing shows a hollow generally cylindrical metal extension member 52 partially embedded at its lower end in the shot and balls located in the mold cavity.
- the extension member has a flat, annular radial flange S4 affixed to its upper edge and coaxially aligned with cylindrical walls of the member, which may be used to secure the punch unit to the sheet metal press assembly.
- the lower portion 56 of the extension member, which is embedded in shot and balls, preferably is bent inwardly so that the extension member will not pull out of the die when the die is removed from the mold after the casting process is completed.
- the extension member should be made of a material, such as steel, which is capable of withstanding the temperatures used in the die making process.
- the step of affixing the die to a structural member to form a punch portion of a sheet metal press assembly may be eliminated by making the die and extension member into an integral unit by the process of the present invention.
- the extension member may be used to pull the die from the mold when the casting process is completed.
- the enclosed furnace 42 illus trated in FIGURE 2 of the drawing may be heated by any suitable means, not shown in the drawing, to raise the temperature of the furnace atmosphere gas which is circulated through the furnace during the die making process of the present invention.
- a gas generator 58 for producing the furnace atmosphere gas and a pump 60 for pumping the furnace gas from the generator through a conduit 62 into the furnace are suitably located outside of the furnace.
- the furnace also is provided with a conduit 64 for venting the furnace atmosphere gas from the furnace during the die making process.
- the furnace gas from the generator preferably is continually circulated in the furnace during the die forming process at a pressure slightly above atmospheric pressure to prevent oxygen from the atmosphere from entering the furnace.
- a reducing atmosphere is used in the process of the present invention to reduce the metal oxides on the shot and steel particles of the die composition and to prevent oxidation of the brazing alloys during the brazing cycle, as will hereinafter be more fully explained.
- a modified dissociated ammonia gas as the furnace atmosphere in the die making process of the present invention.
- the hydrogen concentration of the disassociated ammonia furnace gas preferably is varied during the die forming process from a maximum, by volume, of to a minimum of 2%, as will hereinafter be more fully explained. Therefore, the gas generator 58, which is used in accordance with the process of the present invention, preferably is capable of varying the hydrogen concentration of the furnace gas which is supplied by the generator to the furnace.
- the natural gas assists in removing oxygen and water vapor released from the mold and furnace walls. It also reduces carbon diffusion from the shot particles when steel shot is used and/or replenishes carbon in the steel shot particles if the carbon is depleted.
- the natural gas may be introduced into the furnace by any suitable means, such as introducing it through the pump into the generator gas stream which is fed into the furnace.
- the natural gas concentration should range from about 4% to 5% of the total furnace atmosphere, although the concentration may be varied somewhat according to the conditions in the furnace.
- a conduit 68 is suitably afilxed to the opening 38 in the base plate 32 to vent the gas which passes through the mold 22 from the furnace.
- the gas may be drawn through the mold and conduit 68 by any suitable means. such as suction created by a compressor 70 located outside the furnace.
- the hot furnace gas is preferably cooled by means of a suitable heat exchange 72 before entering the compressor.
- Another conduit 74 may be used to recycle the gas from the compressor into the furnace 42.
- the hot recycle furnace gas from the compressor may be cooled by means of a suitable condenser 76 before being recycled into the furnace.
- a suitable water trap 78 which functions coujointly with the condenser 76, may be provided in the conduit line 74 to remove any entrained moisture in the furnace gas prior to recycling the gas from the compressor to the furnace through the conduit 74.
- the brazing alloys. which are used to form the brazed shot dies of the present invention may be introduced into the mold cavity during the die making process by any suitable means.
- the brazing alloy may be melted by any suitable means and poured into a metal receiving funnel 80 which is suitably located outside the furnace 42.
- the funnel 80 is most advantageously located above the level of the mold 22 so that during the die making process, as will hereinafter be more fully explained, the molten alloy will how by force of gravity through a conduit 86, which is suitably connected to the funnel 80, into another metal receiving funnel 88, suitably positioned above the mold cavity in the furnace.
- the receiving funnel 88, through which the molten brazing alloy flows into the mold cavity may be suspended above the mold cavity by any suitable means, not shown in the drawing.
- brazed shot dies may be produced in accordance with the process of the present invention by using any suitable brazing alloy which will result in the formation of a precision cast-tosize brazed shot die.
- An example of such an alloy is a commercially available product composed of approximately 66%, by weight, copper, 39.25%, by weight of zinc and 0.75% by weight of tin.
- brazing alloys consisting essentially, by weight, of about 35% to 55% copper, about 25% to 40% zinc, about 5% to 25% manganese, about to 10% nickel, about 017: to aluminum, about 0% to 3% silicon, about 0% to tin, and about 0% to 5% antimony.
- the alloys of the above composition ranges also may have trace quantities of other metals, such as phosphorous, cadmium and lead.
- Brazing alloys made from these compositions have a melting temperature ranging from about 1420" F. to about 1650 F.
- a typical analysis of a brazing alloy which is suitable for use in making a brazed shot die in accordance with the process of the present invention is listed in Table IV below:
- the mold 22 is placed in the furnace, and the punch extension member 52 and thermocouples 46 are suitably installed.
- the furnace preferably is gradually heated at a rate of about 30 F. per hour in a modified dissociated ammonia furnace atmosphere containing about 2.5%, by volume, of hydrogen, with the balance being nitrogen, at a pressure slightly above atmospheric pressure.
- a modified dissociated ammonia furnace atmosphere containing about 2.5%, by volume, of hydrogen, with the balance being nitrogen, at a pressure slightly above atmospheric pressure.
- the compressor When the furnace starts to heat, the compressor is cut in with sufficient intake vacuum to draw the furnace gas through the mold cavity 39 and mold 22, thereby heating the shot, balls and mold to cause the mold cavity to expand.
- furnace gas is continually supplied to the furnace 42 by the generator 58 and vented from the furnace through the vent conduit 64 during the entire die making process.
- the temperature differential between the mold and the furnace atmosphere preferably is maintained within a maximum temperature differential of about 160 F. until the furnace atmosphere reaches about 350 F. to prevent the mold of the preferred embodiment of the present invention from cracking.
- the temperature differential may be maintained within a maximum limit of about 300 F.
- natural gas is preferably introduced into the furnace so that the concentration of the natural gas is about 4% of the total furnace atmosphere.
- the hydrogen content of the furnace atmosphere gas preferably is increased to a concentration ranging from about 10% to about by volume, to reduce any metal oxides on the steel shot and balls in the mold cavity.
- the natural gas feed to the furnace atmosphere preferably is turned off.
- the heating of the furnace is continued, and the relatively high hydrogen concentration gas is recycled through the mold by the compressor until the metal oxides on the shot and balls have been reduced and the mold, shot and balls have reached a minimum temperature of about 1650 F. and a maximum temperature of about 1725 F., as indicated by the thermocouples 46 on the instrument box 50. In this temperature range, the
- mold composition of the preferred embodiment of the invention expands so that the mold cavity becomes enlarged. Since the thermal expansion characteristics of the mold are so similar to the thermal shrinkage characteristics of the metallic die composition in the preferred embodiment of the invention at the brazing temperature, the degree of expansion of the mold cavity is not too critical. However, the expansion of the mold cavity during heating must compensate for the size change of the metallic die composition during cooling in accordance with the process of the present invention. Thus, when the furnace is cooled during the cooling cycle of the die making process, the brazed shot die composition of the preferred embodiment of the invention contracts in the mold cavity to the desired final shape and size of the die to be produced, as will hereinafter be more fully explained.
- the compressor is cut ofi.
- the furnace preferably is heated at this temperature for approximately four hours, and the hydrogen concentration of the furnace gas circulated through the furnace by the gas generator 58 preferably is changed to about 2.5%, by volume, in preparation for the brazing step, as will hereinafter be more fully explained.
- hydrogen concentration of the furnace gas is maintained at about 2% to 3%, by volume, a more satisfactory braze is obtained in the die making process of the present invention using the brazing alloys and the shot and balls of the preferred embodiment of the present invention.
- the molten brazing alloy is poured into the funnel so that it flows through the conduit 86 to the receiving funnel 88 and into the mold cavity 39.
- the brazing alloy of the preferred embodiment of the present invention may be melted in any suitable receptacle by any suitable means, not shown in the drawings.
- the alloys of the present invention are melted in the absence of anhydrous borax which acts as a flux and prevents the oxidation of the alloys during the melting step.
- the funnel 8i] Prior to adding the brazing alloy to the mold cavity, conduit 86 and receiving funnel 88 may be treated with a protective coating, such as Fiberfrax QF- 180. to prevent the accumulation of the brazing alloy on these members.
- the temperature of the brazing alloy should not exceed 1650 F. prior to entering the mold cavity to prevent the zinc in the alloys from vaporizing.
- an alloying action occurs in the presence of the steel shot and steel balls in the cavity, and the alloy tends to solidify to form the brazed shot die composition of the present invention.
- the furnace is allowed to cool at a predetermined rate, preferably about 30 F. per hour, in a reducing furnace atmosphere containing about 2.5%, by volume, of hydrogen until the mold temperature is cooled to about 1000" F. to complete the brazing step.
- a predetermined rate preferably about 30 F. per hour
- a reducing furnace atmosphere containing about 2.5%, by volume, of hydrogen
- the furnace heat and gas from the generator most advantageously are turned off, and the die composition is allowed to cool normally to room temperature.
- the die composition of the present invention contracts in the mold cavity to substantially the same initial size and shape of the mold cavity.
- precision cast to-size brazed shot dies can be made by the process of the present invention which substantially reduces the number of post-machining operations required to conform the die to the desired final shape.
- Example I A wooden mold assembly was prepared for forming a ceramic mold having a width of 28 inches, a length of 52 inches and a height of 19.5 inches.
- a rectangular solid plaster model having a width of 15 inches, a length of 39 inches and a height of 1 6 inches was centrally posi tioned in the bottom of the mold assembly so that the side walls of the mold cavity of the mold, which was produced in accordance with the above-described process of the present invention, had a thickness of 6.5 inches and a bottom Wall thickness of 3.5 inches.
- the mold was formed using 1200 pounds of nepheline syenite sand, 72 pounds of sodium silicate and 84 pounds of calcium aluminate.
- the chemical composition of the nepheline syenite and calcium aluminate which was used to form the mold is listed above in Table I and Table II, respectively.
- the sodium silicate which was used had a chemical analysis, by weight, of about 15% SiO about 38% Na O and the balance Water.
- the walls of the mold and the side Walls of the mold cavity were treated in the above-described manner with a ceramic mixture consisting, by weight, of about 17% olivine fiour, about 25% kaolin flour and about 58% sodium silicate.
- a one-inch layer of SAE 1095 steel shot having a mesh size ranging from 40 to 200 mesh was added to the bottom face of the mold cavity.
- Alternate layers of /a-inch diameter SAE 1020 steel balls were added to the mold cavity in the manner previously described to fill the cavity.
- a total of 321 pounds of steel shot and 395 pounds of steel balls were added to the cavity.
- the mold was then placed in a suitable furnace and heated in an atmosphere of hydrogen, nitrogen and natural gas to a temperature of 1700 F. under the process conditions previously described in reference to the preferred embodiment of the present invention.
- a total of 281 pounds of a brazing alloy having a composition as listed in Table IV above was poured into the cavity, and the die composition was then cooled to room temperature under the process conditions previously described.
- the precision cast-tosize brazed shot die produced in this manner had substantially the same size and shape as the initial size and shape of the model used to form the mold cavity.
- FIGURE 3 of the drawing a completed integral punch portion or unit of a sheet metal forming die 90 is illustrated, which may be produced by the process of the present invention, as shown in FIGURE 2 of the drawing.
- the punch unit 90 consists of a precision cast-to-size brazed shot die member 92 and the generally cylindrical extension member 52.
- the punch unit may be used in a suitable sheet metal forming press assembly.
- the precision cast-to-size brazed shot dies produced by the process of the present invention offer several advantages over iron or steel dies which are cast by conventional iron and steel casting processes. Also, the die compositions and mold compositions of the present in vention, when used in accordance With the process of the present invention, make possible the manufacture of precision cast-to-size brazed shot dies. Therefore, the number of post-machining operations required to conform the die to the desired final shape and size is substantially reduced, thereby greatly decreasing the costs involved in forming metal dies. In addition, the brazed shot dies produced by the process of the invention have excellent wear resistance when compared with most cast iron or steel dies produced by a conventional casting technique.
- a method of forming a precision cast-to-size article comprised of steel shot bonded together by a brazing alloy comprising the steps of forming a contoured cavity in a ceramic mold so that the contoured surface of the cavity defining walls of said mold substantially duplicate the size and shape of said brazed steel shot article, said mold comprising a ceramic composition which includes nepheline syenite sand as the base material, and calcium aluminate and water glass as binders, said walls of said mold having a coefiicient of thermal expansion which is substantially equal to the coeflicient of thermal expansion of said steel shot over a temperature range from about room temperature to an elevated temperature of at least the melting point of said brazing alloy, filling said cavity with relatively small steel shot particles and steel filler particles of larger size, said shot particles being sufficiently small so that a capillary action occurs when the molten brazing alloy is added to said cavity to fill the voids between said shot particles and said filler particles in said cavity, heating said mold and
- a method of forming a precision cast-to-size shot die comprised of steel shot particles bonded together by a brazing alloy, said method comprising the steps of forming a contoured mold cavity in a ceramic mold so that the contoured surface of the cavity-defining Walls of said mold substantially duplicates the size and shape of the contoured working face of the metal die ultimately formed in said cavity, said mold comprising, by weight, about to ncpheline syenite sand, about 3% to 10% sodium silicate and about 2% to 10% calcium aluminate, said Walls of said mold having a coefiicient of thermal expansion which is substantially equal to the coefficient of thermal expansion of said steel shot over a temperature range from about room temperature to an elevated temperature of at least the melting point of said braze, covering the lower contoured surface of said cavity with a layer of small steel shot particles, said layer being embodied in the working face of said die to facilitate maching of said working face after said die is formed, filling the remaining portion of said cavity with said steel
- a method of forming a precision cast-to-size brazed shot die comprising the steps of forming a contoured mold cavity in a ceramic mold so that the contoured surface of the cavity-defining walls of said mold substantially duplicates the size and shape of the contoured working face of the die ultimately formed in said cavity, said mold comprising, by weight, about 84% to 91% nepheline syenite sand, about 5% to 8% calcium aluminate, and about 4% to 8% sodium silicate, said wails of said mold having a coefficient of thermal expansion which is substantially equal to the coeflicient of thermal expansion of said shot over a temperature range from about room temperature to an elevated temperature of at least the melting point of said braze, covering the lower contoured surface of said cavity with a thin layer of steel shot particles having a mesh size ranging from about 40 mesh to about +200 mesh, said layer being embodied in said working face of said die to facilitate machining of said working face after said die is formed, said layer having a
- a reducing atmosphere containing, by volume, about 2% to 3% hydrogen and the balance nitrogen to prevent oxidation of said particles, heating said mold from said temperature of about 1400 F. to an elevated temperature range in a reducing atmosphere containing, by volume, at least about 10% to 15% hydrogen to reduce any metal oxides on said particles in said cavity and to cause said cavity to expand, said elevated temperature range varying from about 1650 F.
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Description
April 11, 1967 K. F. JAMES ETAL METHOD OF MAKING SHEET METAL FORMING DIES Filed Aug. 22, 1965 645 GPA/ERA T04? OMPRESSOR HEAT EXCHANGE)? ZyZ llH
INVENTORS 122/2655 fa 5222a BY aprazmr e/00w A T TORNEY 3,313,007 Patented Apr. 11, 1967 3,313,007 METHOD OF MAKING SHEET METAL FORMING DIES Kenneth F. James and Alexander H. Joyce, Detroit,
Mich., assignors to General Motors Corporation, De-
troit, Mich, a corporation of Delaware Filed Aug. 22, 1963, Ser. No. 303,783 7 Claims. (Cl. 22204) This invention relates generally to casting metal ar ticles. More particularly, this invention relates to precision cast-to-size brazed shot dies and to a method of making same.
Most commonly used casting techniques for casting metal articles, such as sheet metal forming dies, involve the step of pouring molten metal, such as cast iron or steel, into a mold cavity which is contoured to the general size and shape of the article to be produced. Molds made of sand or similar ceramic materials are widely used in metal casting processes, since ceramic molds are relatively inexpensive and easy to fabricate. Most commonly used ceramic molds have fairly good structural strength at the relatively high temperatures employed in most commonly used iron or steel casting processes, and also they are relatively resistant to the diffusion of the molten metal into the Walls of the mold cavity during the casting process. However, casting processes, in which metal articles such as cast iron or steel dies are cast in ceramic molds, usually involve problems of size and shape control in forming the article, since the articles which are formed by these processes generally have a somewhat different size and shape than the initial size and shape of the mold cavity.
The problem of controlling the final size and shape of the metal article, such as a steel or cast iron die, formed by most commonly used casting processes generally is attributed to the difference in the characteristics of thermal expansion of the ceramic mold and the characteristics of thermal and solidification shrinkage of the metallic die. In this application, by thermal expansion characteristics of the mold, We refer to the manner in which the mold cavity becomes enlarged and deformed from its initial size and shape on being heated during the casting process. By thermal shrinkage characteristics of the metallic die, we refer to the manner in which the molten metal materials in the mold cavity solidify and contract on cooling to form the die. In other words, shrinkage due to solidification as well as thermal contraction is included in the term thermal shrinkage characteristics." Thus, since the thermal expansion characteristics of a ceramic mold usually differ from the thermal shrinkage characteristics of a metallic casting, metal dies which are made by a casting technique utilizing ceramic molds generally have a different size and shape than the initial size and shape of the mold cavity. Also, when irregular shaped metal .articles or dies are cast in a mold, differential solidification rates between the heavy and light sections of the castings usually cause a considerable amount of distortion. In fact, this latter problem is often the major cause of distortion in casting a metal article or die.
In the past these problems have been compensated for by providing a mold cavity which is somewhat larger than the desired final size of the die to be produced and by casting an oversize die. The excess stock on the die so formed is subsequently removed from the cast die by postmachining operations, such as kellering and barbering, to conform the die to the desired final shape and size. However, these post-machining and handling operations are relatively expensive and diflicult to perform. This is particularly true in casting metal dies for use in sheet metal forming operations, since the size and shape of these dies must be very accurately controlled if the dies are to operate properly in a sheet metal forming press or similar apparatus. Naturally, the post-machining operations and handling steps which are involved contribute greatly to the overall cost of the die making process.
Thus it is desirable to form precision cast-to-size metal dies so that the number of post-machining operations required is substantially reduced, thereby reducing the costs of the die making process. In this application, by precision cast-to-size dies, we refer to dies which are formed by a casting process in which the cast die has substantially the same size and shape as the initial size and shape of the mold cavity. In addition to the advantages that this type of precision casting process offers by eliminating or greatly reducing the number of necessary post-machining op erations, it also offers other process advantages. For instance, such a process eliminates the necessity of forming an enlarged mold cavity and permits the direct use of the die pattern or master model, which are exact duplicates of the die to be produced, to form the mold cavity. Hence, the die which is produced in the mold cavity will have substantially the same size and shape as the master model or die pattern used to form the mold cavity.
The present invention involves a precision casting process utilizing a brazing procedure to form metal articles, such as brazed shot dies. We have found that the brazed shot dies so produced generally have excellent wear resistance which in many cases is superior to com monly used dies which are cast from steel or cast iron. In addition, as will hereinafter be more fully explained, We have found that the process of the present invention, by which small metal shot particles are brazed together to form brazed shot dies, substantially eliminates the problems of solidification shrinkage previously mentioned in the case of casting irregular shaped metal articles having heavy and light sections.
However, as is well-known in the art, most brazing techniques used in making metal articles similar to the brazed shot dies of the present invention generally involve the use of more expensive process steps, equipment and materials than the processes, equipment and materials used in most commonly used casting processes to cast metal articles, such as cast steel or cast iron dies. For instance, brazing techniques often require the use of expensive furnace equipment having a special protective furnace atmosphere to prevent oxidation of the brazing alloy or metal parts which are being brazed together. Also, the brazing alloys and metal shot and filler particles used to form the brazed shot dies of the present invention are generally more expensive materials for use in forming a die than regular tool steel or cast iron.
In addition, even if the previously mentioned problem of differential solidification is substantially eliminated by casting a metal article in a ceramic mold using a brazing alloy to bond metal particles together in the mold cavity, the thermal expansion characteristics of the ceramic mold must be compensated for in order to achieve a precision cast-to-size process for making dies. Otherwise, the number of post-machining operations necessary to conform the die to the desired final shape and the resulting fabrication costs would not be substantially reduced. Thus, if the number of necessary post-machining operations is substantially reduced by providing a process to make precision cast-to-size brazed shot dies, it is possible to greatly reduce the overall cost of fabricating brazed shot dies. Accordingly, the reduction in post-machining costs realized by using a precision casting process to form brazed shot dies would make the use of these dies economically competitive in most applications with the use of cast steel or cast iron dies which are made by most commonly used casting processes and which require substantial postmachining operations. In addition, the superior wear resistance and long life of brazed shot dies offer additional operational advantages over the use of dies cast from steel or cast iron in many applications, such as sheet metal forming processes. A process for making precision cast-to-size brazed shot dies has not heretofore been recognized.
Therefore, it is a principal object of the present inven tion to provide a method of making articles formed of metal particles or shot which are bonded together by a brazing alloy wherein a mold composition is provided having a thermal coefficient of expansion substantially equal to the thermal coefficient of expansion of the metal particles or shot over the temperature range from about room temperature to the pouring temperature of the brazing alloy.
It is another object of the present invention to provide a method of producing precision cast-to-size brazed shot dies to greatly reduce the number of post-machining operations which are required to conform the dies to the desired shape and size, thereby reducing the overall costs involved in making sheet metal forming dies.
It is a further object of the present invention to provide a method of producing precision cast-to-size brazed shot dies having high strength and wear resistance for use in a sheet metal forming press assembly.
In accordance with the present invention, these and other objects are accomplished by providing a mold cavity in a ceramic mold having a thermal coefficient of expansion, over the temperature range employed in the casting process, which is substantially equal to the coefficient of thermal expansion of the brazed shot die composition which is cast in the mold cavity to make the die. The process of making the precision cast-to-size brazed shot dies of the present invention involves the steps of providing a master model having the exact size and shape of the die which is to be produced, positioning the model in a suitable mold assembly, pouring a suitably mixed mold composition into the mold assembly over the model, curing the mold composition to form a ceramic mold and subsequently removing the cured mold from the mold assembly and the model from the mold to provide the mold cavity.
Metal shot and metal filler particles are next placed in the mold cavity in the desired arrangement, and the mold is placed in a suitable furnace and heated in a suitable protective atmosphere to a suitable temperature level above the pouring temperature of the brazing alloy which is to be used. When the mold has reached this temperature, a molten brazing alloy is poured into the mold cavity over the heated shot and fillter particles to fill the voids therebetween, and the ceramic mold and metal composition in the mold cavity are subsequently cooled in the furnace so that the alloy solidifies and brazcs the metal shot and metal particles together to form the brazed shot die embodying the present invention. On cooling, the die compositions of the present invention solidify and contract, thereby shrinking to the same extent as the mold cavity expands on heating, so that the brazed shot die which is formed has substantially the same size and shape as the initial shape of the mold cavity when the model is removed. The precision cast-to-size brazed shot die is subsequently removed from the mold cavity. Since the die which is formed by the process of the present invention has substantially the same size and shape as the model used to form the mold cavity, the number and extent of post-machining and handling operations necessary to conform the die to the desired final shape is greatly reduced.
Other features and advantages of the present invention will be apparent from the following description of certain embodiments thereof, taken in conjunction with the accompanying drawing, in which:
FIGURE 1 is a perspective view, with parts broken away, of a mold assembly which may be used to form the mold embodying the present invention;
FIGURE 2 is a vertical clevational view, with parts broken away and in section, of a furnace assembly and appurtenances which may be used in accordance with the proce s of the present invention to make the precision cast-to-size brazed shot dies of the present invention; and
FlGURE 3 is a vertical elevational view, with parts broken away and in section, of a precision cast-to-size brazed shot die embodying the present invention.
Referring to FIGURE 1 of the drawing, a typical mold assembly is illustrated which may be used to form the ceramic mold embodying the present invention. Four rectanguiar, plate-like wall members I!) are vertically mounted on a fiat, rectangular base member 12 to form a cubical mold cavity 14 which opens upwards. The wall members and the base member may be made of wood or any other suitable material. These members may be detachably but firmly secured to one another by any suitable means, such as dowel pins, which are not shown in the drawing.
A master die pattern or model 16 having a contoured upper surface 18 which exactly duplicates the size and shape of the die to be produced, and a flat base surface 20, is suitably positioned in the cavity 14 so that the flat base surface 20 of the model is firmly positioned on the flat base member 12, and the upper contoured surface of the model protrudes into the cavity. As previously men tioned, the precision casting process of the present invention permits the direct use of a duplicate model of the die to be produced, since the necessity of casting an oversize die is eliminated. Naturally, this is an important advantage of the present invention. The model may be made of plaster or any other suitable material, such as plastic.
Prior to forming the mold, the upper contoured surface 13 of the model preferably is treated in a conventional manner with any suitable parting agent or mold release agent. such as a silicone oil, to facilitate removal of the model after the mold has been formed. We have found that a parting agent which is commercially marketed under the trade name Aristo No. 5950" is suitable for use with a plaster model and the ceramic mold compositions of the present invention.
As previously mentioned, the present invention con templates the use of mold compositions having thermal expansion characteristics which are substantially equal to the thermal shrinkage characteristics of the brazed shot die compositions of the present invention, so that the aforementioned problems of size and shape control, which arise due to dilferences in these characteristics, are greatly reduced or eliminated. In the present invention, we contemplate the use of a mold comprising, on a weight basis, about to nepheline syenite sand as the base material with about 3% to 10% sodium silicate and 2% to 10% calcium aluminate as binders, In the preferred embodiment of the present invention, the mold has a composition, by weight, of about 84% to 91% nepheline syenite, about 5% to 8% calcium aluminate and about 4% to 8% sodium silicate.
Nepheline syenite is a commercially available ceramic material which consists essentially of a mixture of several different sodium aluminum silicates and potassium aluminum silicates. A typical analysis of nepheline syenite on a volumetric percent basis which is suitable for use in the process of the present invention is listed in Table I below:
TABLE I Percent by Mineral composition of nepheline syenite: volume Albite 54 Microcline 20 Nepheline 2O Muscovite 2 Mafics 2 Balance (Biotite, Hastingsite, Magnetite) 2 Total "W0 In the preferred embodiment of the present invention, we contemplate the use of nepheline syenite having a mesh size ranging from 20 to 40 mesh. Naturally, it will be appreciated that the mesh size and the mineral composition of the nepheline syenite may be varied somewhat from the composition listed in Table I and the mesh size specified in the preferred embodiment of the invention. Of course, since these variations or changes will have some etTect on the thermal expansion characteristics of the molds used in accordance with the process of the present invention, corresponding changes must also be made in the thermal shrinkage characteristics of the brazed shot die compositions of the present invention. In general, we have found that the use of smaller mesh nepheline syenite results in the mold having a smaller coefiicient of thermal expansion and, conversely, the use of larger mesh nepheline syenite results in a mold having a greater coefficient of thermal expansion.
As previously mentioned, an aqueous solution of sodium silicate or waterglass and calcium aluminate are used conjointly to bind the ceramic mold compositions used in the process of the present invention. In the preferred embodiment of the present invention, we contemplate the use of a viscous, aqueous solution of sodium silicate having an Na O content ranging, by weight, from about 14.8% to 15.2% and SiO content ranging, by weight, from about 28% to 29% with the balance being water. In the preferred embodiment of the present invention, the calcium aluminate cement which is used preferably is in the form of a finely divided powder having a mesh size of less than 100 mesh. Most commercially available grades of calcium aluminate cements having a calcium aluminate content, by weight, in excess of about 90% are suitable for use in the present invention. A typical chemical analysis of calcium aluminate which is suitable for use in forming a mold embodying the present invention is listed in Table II below:
TABLE II Percent by Chemical constituents of calcium aluminate: weight AI O 79.0 SiO 0.1 Fe O 0.3 Na O 0.5 CaO 18.0 MgO 0.4 Loss on ignition 1.7
Total 100 In forming the mold of the present invention, the sodium silicate and the calcium aluminate binders are mixed in a suitable mulling apparatus with the nepheline syenite sand. Preferably, the nepheline syenite sand and cal cium aluminate powder are added to the mulling machine and mulled for about 1 /2 to 3 minutes to thoroughly mix the powders. The sodium silicate solution preferably is next slowly added to the powdered mixture and mulled for about 2 to 3 minutes until a moist, sandy mass is formed.
The ceramic mixture is subsequently poured into the cavity 14 of the mold assembly to form the mold 22. The mixture is most advantageously added in small separate portions with each portion being firmly packed in the cavity by using any suitable device, such as a pneumatic rammer, until the last portion is added and packed so that the cavity 14 is completely filled. The progressive packing after each portion of the ceramic mixture is added serves to eliminate voids in the cavity of the mold assembly. In the preferred embodiment of the present invention, when relatively large articles or dies are being cast, the thickness of the ceramic mixture between the walls of the mold assembly and the model 16 preferably ranges from about 6 inches to 12 inches, and the thickness of the mold between the top of the cavity and the model preferably ranges from about 2%. inches to 6 inches to minimize the temperature gradient across the mold walls, thereby preventing cracking of the mold during the die forming process. These dimensions are not too critical when relatively small articles or dies are being made by the process of the present invention using a relatively small mold.
Prior to curing the sand mixture, the excess sand at the top of the cavity 14 preferably is leveled off with the top surface of the cavity walls 10 by any suitable means, such as by scraping the excess sand off with a straight edge. A shallow cylindrical opening 24 and a plurality of shallow elongated grooves 26, which extend radially from the opening, may be formed in the leveled top surface 28 of the mold 22 directly above the model 16 in the cavity 1.4. The opening and grooves facilitate the heating of the mold and the die composition when large dies are being cast by providing a path for the distribution of the furnace atmosphere gas through the die compostion and walls of the mold cavity during the heating cycle 'of the casting process, which will hereinafter be more fully described. Also, as will hereinafter be more fully explained, smaller dies or castings which are made using smaller molds do not necessarily require gas flow through them, except to reduce the moisture content 'of the mold.
Since it is desirable to concentrate the path of the furnace gas through the mold cavity, an asbestos rope seal 30 or similar sealing material, which can withstand high temperatures, preferably is positioned in a groove provided in the top surface 28 of the mold 22 surrounding the opening 24 and the grooves 26. The seal 30 serves to prevent the furnace atmosphere gas from being drawn from the furnace between the top surface 28 of the ceramic mold and the rectangular metal base plate 32 which is used to support the mold in the furnace during the heating cycle of the casting process. The metal base plate 32 may be made of steel or other suitable material which is capable of withstanding the high temperatures employed in the furnace.
The base plate 32 may be aflixed to the top of the mold assembly by any suitable means, such as tie studs, 34, which extend from the top surface of the walls 10 of the mold assembly into openings 36 provided in the base plate. Preferably, the base plate is positioned so that a flush fit is obtained between the plate and the leveled top surface of the sand mixture. The base plate 32 also is provided with a cylindrical opening 38 which extends through the top and bottom surfaces of the plate so that it is coaxially aligned and in communication with the cylindrical opening 24 in the top surface 28 of the sand mixture. As previously mentioned, hot furnace atmosphere gas is drawn through this opening during the casting process.
Prior to affixing the metal base plate on top of the mold assembly and ceramic mixture, the surface of the base plate which contacts the mixture preferably is treated with a protective coating to prevent oxidation of the base plate and sticking of the mold to the base plate during the casting process. We have found that a suitable ceramic coating for this purpose is commercially marketed under the trade name of Fiberfrax QF180. This material is a viscous suspension of finely divided, powdered inorganic materials in water and has a total solids content of about 69%. by weight. The total solids content of the material consists essentially, by weight, of about 57% silicon dioxide, about 41% alumina and the balance including small quantities of sodium oxide, boron oxide, magnesium oxide and traces of other inorganic materials.
After the base plate has been affixed to the mold assembly, the mold assembly may be inverted by any suitable means so that the ceramic mixture rests firmly on the metal base plate 32. The mixture preferably is allowed to cure at room temperature for an initial curing period of about 1 to 2 hours with the mold assembly in place. The mixture is substantially cured during this initial curing period and forms a relatively firm mold. After the mold is substantially cured during this initial curing cycle. the wooden members of the mold assembly and the pattern or model 16 are removed by any suitable means. Preferably, the mold is covered with a plastic sheet, such as polyethylene, and allowed to stand for about 48 hours to complete the cure. The polyethylene sheet serves to retain moisture in the mold, thereby aiding the formation of chemical bonds which harden the mold during the mold curing cycle.
The chemical reactions which take place during the curing cycle between the calcium aluminate and the sodium silicate binders and the nepheline syenite sand base are very complex and not too Well understood. However, it is believed that the calcium aluminate causes the so dium silicate to set up and form alkaline earth metalsodium silicate bonds in the ceramic mixture. The cured mold thus formed has excellent strength and high resistance to cracking when used in the process of the present invention to form the precision cast-to-size brazed slot dies of the present invention.
After the mold cure is completed, the outer side walls and top surfaces of the mold preferably are treated with a suitable heat-resistant ceramic coating to make these surfaces substantially impervious to the passage of the furnace atmosphere gas from the furnace through these surfaces during the heating cycle of the casting process. The upper wall portion of the mold cavity also preferably is treated with a ceramic coating. However, the lower face portion of the mold cavity preferably is not treated so that the furnace atmosphere gas may pass through this portion of the mold cavity during the heating cycle of the casting process, as will hereinafter be more fully described.
In the preferred embodiment of the present invention, we contemplate the use of a ceramic coating material consisting. by weight, of about 17% olivine Hour, kaolin powder and about 58% sodium silicate. The olivine flour preferably has a mesh size ranging from 180 mesh to about 220 mesh. The kaolin powder preferably has a mesh size of less than 350 mesh. The sodium silicate used in the coating preferably has the same composition as the previously mentioned sodium silicate composition used in forming the mold. Of course, it will be appreciated that other ceramic coating materials may be used to coat the mold surfaces for the above-mentioned purposes in accordance with the process of the present invention.
The ceramic coating mixture in the preferred embodiment of the present invention may be prepared by mixing the ingredients in any suitable mixing apparatus until a viscous mixture is formed. The mixture is then applied to the above-mentioned mold surfaces by any suitable means, such as a paint brush, until these surfaces are substantially impregnated with the coating and are relatively impervious. In this manner, the flow of furance atmosphere gas through the mold during the heating cycle of the die making process is substantially confined to a path through the bottom surface of the mold cavity and the opening 24 in the bottom of said mold. Also, we have found that this coating increases the strength of the mold against cracking.
FIGURE 2 of the drawing illustrates the method by which the precision cast-to-size brazed shot dies of the present invention are made. The cured ceramic mold 22 is positioned on the metal base plate 32 with the mold cavity 39 opening upwards. The base plate is suitably mounted on pedestals 40 within an enclosed furance 42 which may be heated by any suitable means, not shown in the drawing.
As previously mentioned, the brazed shot die compositions of the present invention have compensatory thermal shrinkage characteristics relative to the thermal expansion characteristics of the mold compositions of the present invention. In casting relatively large dies by the precision casting process of the present invention, we contemplate the use of relatively small metal shot particles and relatively large metal filler particles. When relatively small dies or metal articles having the size of about a six-inch cube or less are made by the process of the present inven tion, the metal filler particles may be omitted from the die composition.
In the preferred embodiment of the present invention for making relatively large dies or metal articles, we contemplate the use of steel shot having a mesh size ranging from about 40 to 200 mesh and filler particles consisting of small diameter steel balls ranging in diameter from approximately inch to inch. The shot and balls may be made of any suitable steel, such as SAE 1095 steel, or other suitable metal. It should be appreciated that the size, shape and composition of the shot and filler particles is not limited to the size, shape and composition of the shot and filler particles of the preferred embodiment of the invention. In other words, these characteristics of the shot and filler particles may be varied if corresponding changes are made in the mold composition so that the thermal shrinkage characteristics of the die composition are compensatory relative to the thermal expansion characteristics of the mold in accordance with the process of the present invention. Preferably, the shot is sufficiently small so that capillary action occurs when the molten brazing alloy is poured into the mold cavity to braze the shot and particles together, as will hereinafter be more fully explained. A typical analysis of steel shot used in the preferred embodiment of the present invention is listed in Table III below:
TABLE III Screen Mesh Size iIlincir Mosh Dimension Percent Shot; Retained in Inches on Sari-en till 10 maximum. OUT R0 maximum. .0029 lot).
Prior to placing the shot and balls in the mold cavity, they preferably are thoroughly cleaned by any suitable means to remove dust and other impurities which may interfere with the brazing process. When the process of the present invention used to form a sheet metal forming die, and since the brazed shot material has superior qualities as a draw die surface than the relatively large filler particles, it is desirable to keep the filler material away from the working surface of the die which is made for such an application. Thus, after the shot has been cleaned, a portion of shot may be added to the mold cavity 39 to cover the lower face 43 of the cavity when the die is to be used in a sheet metal forming press assembly. In the preferred embodiment of the present invention, the layer of shot 42 so added preferably ranges in thickness from about /2 inch to about 1 /2 inches. Another advantage of providing this layer of small diameter shot on the lower portion of the die is that it facilitates the machining and finishing of the die after the casting process is completed.
After the layer of shot 42 has been added to the lower face of the cavity, a portion of the steel ball filler particles is poured into the mold cavity over the layer of shot to fill a part of the upper portion 44 of the mold cavity. Subsequently, a portion of the small diameter shot is also added to the upper portion of the cavity to fill the voids between the balls. The steel balls and shot most advantageously are poured into the cavity in successive alternate layers until the cavity is filled. The shot and balls may be vibrated after each addition by any suitable means to insure that they are tightly packed in the mold cavity. In addition to the strength and shrinkage characteristics they impart to the dies, the balls also are a relatively cheap filler material and substantially reduce the cost of producing the larger sized brazed shot dies of the present invention.
The brazed shot die which is formed by the process illustrated in FIGURE 2 is typical of a punch portion of a sheet metal forming die. When a punch die is used in a sheet metal press assembly, it is usually afiixed to a movable member in the sheet metal press assembly by Welding or mechanically locking the die to the member. In the present invention, an extension member for positioning the die in a sheet metal press assembly may be partially embedded in the shot and balls in the mold cavity so that when the die is cast the extension member and the die are formed into an integral punch unit.
For instance, FIGURE 2 of the drawing shows a hollow generally cylindrical metal extension member 52 partially embedded at its lower end in the shot and balls located in the mold cavity. The extension member has a flat, annular radial flange S4 affixed to its upper edge and coaxially aligned with cylindrical walls of the member, which may be used to secure the punch unit to the sheet metal press assembly. The lower portion 56 of the extension member, which is embedded in shot and balls, preferably is bent inwardly so that the extension member will not pull out of the die when the die is removed from the mold after the casting process is completed. Of course, the extension member should be made of a material, such as steel, which is capable of withstanding the temperatures used in the die making process. Thus, the step of affixing the die to a structural member to form a punch portion of a sheet metal press assembly may be eliminated by making the die and extension member into an integral unit by the process of the present invention. Also, the extension member may be used to pull the die from the mold when the casting process is completed.
As previously mentioned, the enclosed furnace 42 illus trated in FIGURE 2 of the drawing may be heated by any suitable means, not shown in the drawing, to raise the temperature of the furnace atmosphere gas which is circulated through the furnace during the die making process of the present invention. As shown in FIGURE 2, a gas generator 58 for producing the furnace atmosphere gas and a pump 60 for pumping the furnace gas from the generator through a conduit 62 into the furnace are suitably located outside of the furnace. The furnace also is provided with a conduit 64 for venting the furnace atmosphere gas from the furnace during the die making process. The furnace gas from the generator preferably is continually circulated in the furnace during the die forming process at a pressure slightly above atmospheric pressure to prevent oxygen from the atmosphere from entering the furnace.
Preferably, a reducing atmosphere is used in the process of the present invention to reduce the metal oxides on the shot and steel particles of the die composition and to prevent oxidation of the brazing alloys during the brazing cycle, as will hereinafter be more fully explained. In the preferred embodiment of the present invention, we contemplate the use of a modified dissociated ammonia gas as the furnace atmosphere in the die making process of the present invention. The hydrogen concentration of the disassociated ammonia furnace gas preferably is varied during the die forming process from a maximum, by volume, of to a minimum of 2%, as will hereinafter be more fully explained. Therefore, the gas generator 58, which is used in accordance with the process of the present invention, preferably is capable of varying the hydrogen concentration of the furnace gas which is supplied by the generator to the furnace.
We have also found it desirable in most cases to add a small amount of natural gas to the furnace atmosphere during a certain stage of the heating cycle of the die making process, as will hereinafter be more fully explained. The addition of the natural gas assists in removing oxygen and water vapor released from the mold and furnace walls. It also reduces carbon diffusion from the shot particles when steel shot is used and/or replenishes carbon in the steel shot particles if the carbon is depleted. The natural gas may be introduced into the furnace by any suitable means, such as introducing it through the pump into the generator gas stream which is fed into the furnace. Preferably, the natural gas concentration should range from about 4% to 5% of the total furnace atmosphere, although the concentration may be varied somewhat according to the conditions in the furnace.
As previously mentioned, the furnace atmosphere gas is circulated through the mold and die composition during the heating cycle of the die making process of the present invention. In this manner the mold, shot and filler balls are heated, and the mold cavity is expanded to a sufficient degree prior to introducing the brazing alloy into the mold cavity during the (lie making process. As shown in FIGURE 2 of the drawing, a conduit 68 is suitably afilxed to the opening 38 in the base plate 32 to vent the gas which passes through the mold 22 from the furnace. The gas may be drawn through the mold and conduit 68 by any suitable means. such as suction created by a compressor 70 located outside the furnace. The hot furnace gas is preferably cooled by means of a suitable heat exchange 72 before entering the compressor. Another conduit 74 may be used to recycle the gas from the compressor into the furnace 42. The hot recycle furnace gas from the compressor may be cooled by means of a suitable condenser 76 before being recycled into the furnace.
It is desirable to minimize the moisture content of the gas circulating in the furnace to prevent oxidation of the steel shot and balls during the heating cycle of the die making process. When the circulating furnace gas passes through the mold, it picks up moisture from the mold. Therefore, a suitable water trap 78, which functions coujointly with the condenser 76, may be provided in the conduit line 74 to remove any entrained moisture in the furnace gas prior to recycling the gas from the compressor to the furnace through the conduit 74.
The brazing alloys. which are used to form the brazed shot dies of the present invention, may be introduced into the mold cavity during the die making process by any suitable means. For instance, the brazing alloy may be melted by any suitable means and poured into a metal receiving funnel 80 which is suitably located outside the furnace 42. The funnel 80 is most advantageously located above the level of the mold 22 so that during the die making process, as will hereinafter be more fully explained, the molten alloy will how by force of gravity through a conduit 86, which is suitably connected to the funnel 80, into another metal receiving funnel 88, suitably positioned above the mold cavity in the furnace. The receiving funnel 88, through which the molten brazing alloy flows into the mold cavity, may be suspended above the mold cavity by any suitable means, not shown in the drawing.
It will be appreciated, of course, that brazed shot dies may be produced in accordance with the process of the present invention by using any suitable brazing alloy which will result in the formation of a precision cast-tosize brazed shot die. An example of such an alloy is a commercially available product composed of approximately 66%, by weight, copper, 39.25%, by weight of zinc and 0.75% by weight of tin. However, in the preferred embodiment of the present invention, we contemplate the use of brazing alloys consisting essentially, by weight, of about 35% to 55% copper, about 25% to 40% zinc, about 5% to 25% manganese, about to 10% nickel, about 017: to aluminum, about 0% to 3% silicon, about 0% to tin, and about 0% to 5% antimony. The alloys of the above composition ranges also may have trace quantities of other metals, such as phosphorous, cadmium and lead. Brazing alloys made from these compositions have a melting temperature ranging from about 1420" F. to about 1650 F. A typical analysis of a brazing alloy which is suitable for use in making a brazed shot die in accordance with the process of the present invention is listed in Table IV below:
TABLE IV Alloy component: Percentage, by Weight Copper 45 Zinc 29 Manganese l5 Phosphorous maximum Cadmium do .04 Lead zdo z .05
After the mold cavity 39 has been filled with the steel shot and balls in the above-described manner, the mold 22 is placed in the furnace, and the punch extension member 52 and thermocouples 46 are suitably installed. The furnace preferably is gradually heated at a rate of about 30 F. per hour in a modified dissociated ammonia furnace atmosphere containing about 2.5%, by volume, of hydrogen, with the balance being nitrogen, at a pressure slightly above atmospheric pressure. During the initial heating stages of the die making process, it is desirable to maintain the hydrogen concentration of the gas from the generator at this level to prevent an explosive gas mixture from forming in the furnace.
When the furnace starts to heat, the compressor is cut in with sufficient intake vacuum to draw the furnace gas through the mold cavity 39 and mold 22, thereby heating the shot, balls and mold to cause the mold cavity to expand. Of course, as previously mentioned, furnace gas is continually supplied to the furnace 42 by the generator 58 and vented from the furnace through the vent conduit 64 during the entire die making process. As the furnace is gradually heated, the temperature differential between the mold and the furnace atmosphere preferably is maintained within a maximum temperature differential of about 160 F. until the furnace atmosphere reaches about 350 F. to prevent the mold of the preferred embodiment of the present invention from cracking. As the furnace temperature is raised above 350 F., the temperature differential may be maintained within a maximum limit of about 300 F. As the furnace temperature is raised to about 1200 F., natural gas is preferably introduced into the furnace so that the concentration of the natural gas is about 4% of the total furnace atmosphere. When the furnace temperature reaches about 1400 F., the hydrogen content of the furnace atmosphere gas preferably is increased to a concentration ranging from about 10% to about by volume, to reduce any metal oxides on the steel shot and balls in the mold cavity. At about 1550" F, the natural gas feed to the furnace atmosphere preferably is turned off.
The heating of the furnace is continued, and the relatively high hydrogen concentration gas is recycled through the mold by the compressor until the metal oxides on the shot and balls have been reduced and the mold, shot and balls have reached a minimum temperature of about 1650 F. and a maximum temperature of about 1725 F., as indicated by the thermocouples 46 on the instrument box 50. In this temperature range, the
mold composition of the preferred embodiment of the invention expands so that the mold cavity becomes enlarged. Since the thermal expansion characteristics of the mold are so similar to the thermal shrinkage characteristics of the metallic die composition in the preferred embodiment of the invention at the brazing temperature, the degree of expansion of the mold cavity is not too critical. However, the expansion of the mold cavity during heating must compensate for the size change of the metallic die composition during cooling in accordance with the process of the present invention. Thus, when the furnace is cooled during the cooling cycle of the die making process, the brazed shot die composition of the preferred embodiment of the invention contracts in the mold cavity to the desired final shape and size of the die to be produced, as will hereinafter be more fully explained.
After the mold, shot and balls have been heated to a temperature within the above-mentioned temperature range and the dew point of the furnace has dropped to a maximum of about 10 F., indicating that the steel shot and balls have been adequately cleaned, the compressor is cut ofi. The furnace preferably is heated at this temperature for approximately four hours, and the hydrogen concentration of the furnace gas circulated through the furnace by the gas generator 58 preferably is changed to about 2.5%, by volume, in preparation for the brazing step, as will hereinafter be more fully explained. We have found that if hydrogen concentration of the furnace gas is maintained at about 2% to 3%, by volume, a more satisfactory braze is obtained in the die making process of the present invention using the brazing alloys and the shot and balls of the preferred embodiment of the present invention.
After the furnace has been maintained at a temperature of about 1700 F. for about four hours in a furnace atmosphere having a hydrogen concentration of about 2.5%, the molten brazing alloy is poured into the funnel so that it flows through the conduit 86 to the receiving funnel 88 and into the mold cavity 39. The brazing alloy of the preferred embodiment of the present invention may be melted in any suitable receptacle by any suitable means, not shown in the drawings. Preferably, the alloys of the present invention are melted in the absence of anhydrous borax which acts as a flux and prevents the oxidation of the alloys during the melting step. Prior to adding the brazing alloy to the mold cavity, the funnel 8i], conduit 86 and receiving funnel 88 may be treated with a protective coating, such as Fiberfrax QF- 180. to prevent the accumulation of the brazing alloy on these members.
As the molten alloy gradually flows into the mold cavity during the brazing cycle, a capillary action occurs, and the alloy is dispersed throughout the cavity to completely fill the voids in the cavity between the shot and balls. In adding the brazing alloys of the preferred embodiment of the present invention to the mold cavity, the temperature of the brazing alloy should not exceed 1650 F. prior to entering the mold cavity to prevent the zinc in the alloys from vaporizing. As the brazing alloy is added to the expanded mold cavity, an alloying action occurs in the presence of the steel shot and steel balls in the cavity, and the alloy tends to solidify to form the brazed shot die composition of the present invention.
After sufficient brazing alloy has been added to the mold cavity, the furnace is allowed to cool at a predetermined rate, preferably about 30 F. per hour, in a reducing furnace atmosphere containing about 2.5%, by volume, of hydrogen until the mold temperature is cooled to about 1000" F. to complete the brazing step. When the mold has reached this temperature, the furnace heat and gas from the generator most advantageously are turned off, and the die composition is allowed to cool normally to room temperature.
As previously mentioned, on cooling to room temperature, the die composition of the present invention contracts in the mold cavity to substantially the same initial size and shape of the mold cavity. Thus, precision cast to-size brazed shot dies can be made by the process of the present invention which substantially reduces the number of post-machining operations required to conform the die to the desired final shape.
The following is a specific example of a precision castto-size brazed shot die produced by the above-described process of the preferred embodiment of the present invention using the preferred mold and die compositions:
Example I A wooden mold assembly was prepared for forming a ceramic mold having a width of 28 inches, a length of 52 inches and a height of 19.5 inches. A rectangular solid plaster model having a width of 15 inches, a length of 39 inches and a height of 1 6 inches was centrally posi tioned in the bottom of the mold assembly so that the side walls of the mold cavity of the mold, which was produced in accordance with the above-described process of the present invention, had a thickness of 6.5 inches and a bottom Wall thickness of 3.5 inches. The mold was formed using 1200 pounds of nepheline syenite sand, 72 pounds of sodium silicate and 84 pounds of calcium aluminate. The chemical composition of the nepheline syenite and calcium aluminate which was used to form the mold is listed above in Table I and Table II, respectively. The sodium silicate which was used had a chemical analysis, by weight, of about 15% SiO about 38% Na O and the balance Water. After the mold was cured and the model was removed to form the mold cavity, the walls of the mold and the side Walls of the mold cavity were treated in the above-described manner with a ceramic mixture consisting, by weight, of about 17% olivine fiour, about 25% kaolin flour and about 58% sodium silicate.
A one-inch layer of SAE 1095 steel shot having a mesh size ranging from 40 to 200 mesh was added to the bottom face of the mold cavity. Alternate layers of /a-inch diameter SAE 1020 steel balls were added to the mold cavity in the manner previously described to fill the cavity. A total of 321 pounds of steel shot and 395 pounds of steel balls were added to the cavity. The mold was then placed in a suitable furnace and heated in an atmosphere of hydrogen, nitrogen and natural gas to a temperature of 1700 F. under the process conditions previously described in reference to the preferred embodiment of the present invention. A total of 281 pounds of a brazing alloy having a composition as listed in Table IV above was poured into the cavity, and the die composition was then cooled to room temperature under the process conditions previously described. The precision cast-tosize brazed shot die produced in this manner had substantially the same size and shape as the initial size and shape of the model used to form the mold cavity.
Referring to FIGURE 3 of the drawing, a completed integral punch portion or unit of a sheet metal forming die 90 is illustrated, which may be produced by the process of the present invention, as shown in FIGURE 2 of the drawing. The punch unit 90 consists of a precision cast-to-size brazed shot die member 92 and the generally cylindrical extension member 52. The punch unit may be used in a suitable sheet metal forming press assembly.
The precision cast-to-size brazed shot dies produced by the process of the present invention offer several advantages over iron or steel dies which are cast by conventional iron and steel casting processes. Also, the die compositions and mold compositions of the present in vention, when used in accordance With the process of the present invention, make possible the manufacture of precision cast-to-size brazed shot dies. Therefore, the number of post-machining operations required to conform the die to the desired final shape and size is substantially reduced, thereby greatly decreasing the costs involved in forming metal dies. In addition, the brazed shot dies produced by the process of the invention have excellent wear resistance when compared with most cast iron or steel dies produced by a conventional casting technique.
While we have described our invention in terms of certain preferred embodiments, it is not to be limited thereby, and it should be understood that other varia tions may be apparent to those skilled in the art and are within the intended scope of the invention as defined by the following claims.
We claim:
1. A method of forming a precision cast-to-size article comprised of steel shot bonded together by a brazing alloy, said method comprising the steps of forming a contoured cavity in a ceramic mold so that the contoured surface of the cavity defining walls of said mold substantially duplicate the size and shape of said brazed steel shot article, said mold comprising a ceramic composition which includes nepheline syenite sand as the base material, and calcium aluminate and water glass as binders, said walls of said mold having a coefiicient of thermal expansion which is substantially equal to the coeflicient of thermal expansion of said steel shot over a temperature range from about room temperature to an elevated temperature of at least the melting point of said brazing alloy, filling said cavity with relatively small steel shot particles and steel filler particles of larger size, said shot particles being sufficiently small so that a capillary action occurs when the molten brazing alloy is added to said cavity to fill the voids between said shot particles and said filler particles in said cavity, heating said mold and particles to about said elevated temperature above the melting temperature of said brazing alloy in a reducing atmosphere, pouring molten brazing alloy into said enlarged cavity to fill said voids in said cavity between said shot particles and said filler particles, said alloy having a composition consisting of essentially of copper, zinc and manganese, cooling said mold in said reducing atmosphere so that said alloy solidifies and brazes said shot particles and said filler particles to form said article and subsequently remove said article from said cavity.
2. A method of forming a precision cast-to-size shot die comprised of steel shot particles bonded together by a brazing alloy, said method comprising the steps of forming a contoured mold cavity in a ceramic mold so that the contoured surface of the cavity-defining Walls of said mold substantially duplicates the size and shape of the contoured working face of the metal die ultimately formed in said cavity, said mold comprising, by weight, about to ncpheline syenite sand, about 3% to 10% sodium silicate and about 2% to 10% calcium aluminate, said Walls of said mold having a coefiicient of thermal expansion which is substantially equal to the coefficient of thermal expansion of said steel shot over a temperature range from about room temperature to an elevated temperature of at least the melting point of said braze, covering the lower contoured surface of said cavity with a layer of small steel shot particles, said layer being embodied in the working face of said die to facilitate maching of said working face after said die is formed, filling the remaining portion of said cavity with said steel shot particles and steel filler particles of larger size, said shot particles being intermingled with said filler particles, said shot particles being sufficiently small so that a capillary action occurs when the molten brazing alloy is added to said cavity to fill the voids in said cavity between said shot particles and said filler particles, heating said mold to about said elevated temperature above the melting point of said brazc, said mold being heated in a reducing atmosphere to reduce the metal oxides on said particles and to facilitate the brazing of said shot particles and said filler particles together, pouring a molten brazing alloy into said enlarged cavity to fill said voids in said cavity, said alloy comprising, by weight, about 35% to 55% copper. to 40% zinc, and 5% to 25% manganese, cooling said mold in said reducing atmosphere so that said alloy solidifies and hrazes said shot particles and said filler particies together to form said (lie, and subsequently removing said die from said cavity.
3. A method of forming a precision cast-to-size brazed shot die as recited in claim 2 wherein said steel shot particles have a mesh size ranging from about 40 to +200 mesh.
4. A method of forming a precision cast-to-size brazed shot die as recited in claim 2 wherein said steel filler particles have a spherical shape and a diameter ranging from about /3 inch to /8 inch.
5. A method of forming a precision cast-to-size brazed shot die as recited in claim 2 wherein said layer of shot particles covering said contoured surface of said cavity has a thickness ranging from a minimum of about /2 inch to a maximum of about 1 /2 inch.
6. A method of forming a precision cast-t o-size brazed shot die as recited in claim 2 wherein said layer of shot particles covering said contoured surface of said cavity has a thickness ranging from a minimum of about /2 inch to a maximum of about 1 inch, said shot having a mesh size ranging from about 40 mesh to +200 mesh.
7. A method of forming a precision cast-to-size brazed shot die, said method comprising the steps of forming a contoured mold cavity in a ceramic mold so that the contoured surface of the cavity-defining walls of said mold substantially duplicates the size and shape of the contoured working face of the die ultimately formed in said cavity, said mold comprising, by weight, about 84% to 91% nepheline syenite sand, about 5% to 8% calcium aluminate, and about 4% to 8% sodium silicate, said wails of said mold having a coefficient of thermal expansion which is substantially equal to the coeflicient of thermal expansion of said shot over a temperature range from about room temperature to an elevated temperature of at least the melting point of said braze, covering the lower contoured surface of said cavity with a thin layer of steel shot particles having a mesh size ranging from about 40 mesh to about +200 mesh, said layer being embodied in said working face of said die to facilitate machining of said working face after said die is formed, said layer having a thickness ranging from about /2 inch to 1 /2 inch, filling the remaining portion of said cavity with said shot particles and spherical steel filler particles, said filler particles being intermingled with said shot particles in said cavity, said filler particles having a diameter ranging from about 3/1; inch to A; inch, gradually heating said moid to a temperature of about 1400 F. in a reducing atmosphere containing, by volume, about 2% to 3% hydrogen and the balance nitrogen to prevent oxidation of said particles, heating said mold from said temperature of about 1400 F. to an elevated temperature range in a reducing atmosphere containing, by volume, at least about 10% to 15% hydrogen to reduce any metal oxides on said particles in said cavity and to cause said cavity to expand, said elevated temperature range varying from about 1650 F. to about 1725 F., decreasing the hydrogen content of said atmosphere to a concentration ranging, by volume, from about 2% to 3% when said mold is heated to said elevated temperature range to facilitate the brazing of said particles together, pouring a molten brazing alloy into said enlarged cavity when the temperature of said mold is within said elevated temperature range to cause said alloy to 110w into said cavity and fill the voids between said particles in said cavity, and alloy comprising, by weight, about to 55% copper, 25% to zinc, 5% to 25% manganese,
to 10% nickel, 0% to 5% aluminum, 0% to 3% silicon, 0% to 10% tin and about 0% to 5% antimony, gradually cooling said mold in said atmosphere so that said alloy solidifies and brazes said shot particles and said fiiler particles together to form said die, said die contracting on cooling to substantially attain the initial size and shape of said cavity, and subsequently removing said die from said cavity.
References Cited by the Examiner UNITED STATES PATENTS 48,973 7/1865 Nimmo 22-204 60,745 1/1867 Kirkup 72-476 75,961 2/1868 Neuberger et a1. 72476 667,488 2/1901 Brabrook 106-383 742,109 10/1903 Wurtz 106-383 870,868 11/1907 Custer 249-82 1,547,836 7/1925 Steenstrup 22204 1,547,838 7/1925 Steenstrup 22-204 1,924,874 8/1933 Moore 22-2165 XR 2,184,776 12/1939 Cottrell 22-203 2,809,407 10/1957 Thomson et a1 22-203 2,828,226 3/1958 Goetzel et a1 22-202 XR J. SPENCER OVERHOLSER, Primary Examiner.
V. K. RISING, Assistant Examiner.
UNITED STATES PATENT OFFICE CERTIFICATE OF CORRECTION Patent No. 3,313,007 April 11, 1967 Kenneth F. James et a1.
It is hereby certified that error appears in the above numbered patent requiring correction and that the said Letters Patent should read as corrected below.
Column 2, line 52, for "problem" read problems column 3, line 50, for "fillter" read filler column 7, line 20, for "slot" read shot line 59, for "said" read the column 9 line 70 for "dissassociated" read dissociated column 12, lines 45 and 46, for "absence" read presence column 13, line 31, for "38%" read 28% column 16, line 22, for "and" read said Signed and sealed this 7th day of November 1967.
(SEAL) Attest:
Edward M. nearer, Jr. EDWARD J. BRENNER Attesting Officer Commissioner of Patents
Claims (1)
- 7. A METHOD OF FORMING A PRECISION CAST-TO-SIZE BRAZED SHOT DIE, SAID METHOD COMPRISING THE STEPS OF FORMING A CONTOURED MOLD CAVITY IN A CERAMIC MOLD SO THAT THE CONTOURED SURFACE OF THE CAVITY-DEFINING WALLS OF SAID MOLD SUBSTANTIALLY DUPLICATES THE SIZE AND SHAPE OF THE CONTOURED WORKING FACE OF THE DIE ULTIMATELY FORMED IN SAID CAVITY, SAID MOLD COMPRISING BY WEIGHT, ABOUT 84% TO 91% NEPHELINE SYENITE SAND, ABOUT 5% TO 8% CALCIUM ALUMINATE, AND ABOUT 4% TO 8% SOLIUM SILICATE, SAID WALLS OF SAID MOLD HAVING A COEFFICIENT OF THERMAL EXPANSION WHICH IS SUBSTANTIALLY EQUAL TO THE COEFFICIENT OF THERMAL EXPANSION OF SAID SHOT OVER A TEMPERATURE RANGE FROM ABOUT ROOM TEMPERATURE TO AN ELEVATED TEMPERATURE OF AT LEAST THE MELTING POINT OF SAID BRAZE, COVERING THE LOWER CONTOURED SURFACE OF SAID CAVITY WITH A THIN LAYER OF STEEL SHOT PARTICLES HAVING A MESH SIZE RANGING FROM ABOUT -40 MESH TO ABOUT +200 MESH, SAID LAYER BEING EMBODIED IN SAID WORKING FACE OF SAID DIE TO FACILITATE MACHINING OF SAID WORKING FACE AFTER SAID DIE IS FORMED, SAID LAYER HAVING A THICKNESS RANGING FROM ABOUT 1/2 INCH TO 1 1/2 INCH, FILLING THE REMAINING PORTION OF SAID CAVITY WITH SAID SHOT PARTICLES AND SPHERICAL STEEL FILLER PARTICLES, SAID FILLER PARTICLES BEING INTERMINGLED WITH SAID SHOT PARTICLES IN SAID CAVITY, SAID FILLER PARTICLES HAVING A DIAMETER RANGING FROM ABOUT 3/8 INCH TO 5/8 INCH, GRADUSALLY HEATING SAID MOLD TO A TEMPERATURE OF ABOUT 1400* F. IN A REDUCING ATMOSPHERE CONTAINING, BY VOLUME, ABOUT 2% TO 3% HYDROGEN AND THE BALANCE NITROGEN TO PREVENT OXIDATION OF SAID PARTICLES, HEATING SAID MOLD FROM SAID TEMPERATURE OF ABOUT 1400*F. TO AN ELEVATED TEMPERATURE RANGE IN A REDUCING ATMOSPHERE CONTAINING, BY VOLUME, AT LEAST ABOUT 10% TO 15% HYDROGEN TO REDUCE ANY METAL OXIDES ON SAID PARTICLES IN SAID CAVITY AND TO CAUSE SAID CAVITY TO EXPAND, SAID ELEVATED TEMPERATURE RANGE VARYING FROM ABOUT 1650*F. TO ABOUT 1725*F., DECREASING THE HYDROGEN CONTENT OF SAID ATMOSPHERE TO A CONCENTRATION RANGING, BY VOLUME, FROM ABOUT 2% TO 3% WHEN SAID MOLD IS HEATED TO SAID ELEVATED TEMPERATURE RANGE TO FACILITATE THE BRAZING OF SAID PARTICLES TOGETHER, POURING A MOLTEN BRAZING ALLOY INTO SAID ENLARGED CAVITY WHEN THE TEMPERATURE OF SAID MOLD IS WITHIN SAID ELEVATED TEMPERATURE RANGE TO CAUSE SAID ALLOY TO FLOW INTO SAID CAVITY AND FILL THE VOIDS BETWEEN SAID JPARTICLES IN SAID CAVITY, AND ALLOY COMPRISING, BY WEIGHT, ABOUT 35% TO 55% COPPER, 25% TO 40% ZINC, 5% TO 25% MANGANESE, 0% TO 10% NICKEL, 0% TO 5% ALUMINUM, 0%TO 3% SILICON, 0% TO 10% TIN AND ABOUT 0% TO 5% ANTIMONY, GRADUALLY COOLING SAID MOLD IN SAID ATMOSPHERE SO THAT SAID ALLOY SOLIDIFIES AND BRAZES SAID SHOT JPARTICLES AND SAID FILLER PARTICLES TOGETHER TO FORM SAID DIE, SAID DIE CONTRACTING ON COOLING TO SUBSTANTIALLY ATTAIN THE INITIAL SIZE AND SHAPE OF SAID CAVITY, AND SUBSEQUENTLY REMOVING SAID DIE FROM SAID CAVITY.
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US303783A US3313007A (en) | 1963-08-22 | 1963-08-22 | Method of making sheet metal forming dies |
| US603937A US3422663A (en) | 1963-08-22 | 1966-12-22 | Sheet metal forming dies |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US303783A US3313007A (en) | 1963-08-22 | 1963-08-22 | Method of making sheet metal forming dies |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3313007A true US3313007A (en) | 1967-04-11 |
Family
ID=23173678
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US303783A Expired - Lifetime US3313007A (en) | 1963-08-22 | 1963-08-22 | Method of making sheet metal forming dies |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US3313007A (en) |
Cited By (6)
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| US4509358A (en) * | 1984-03-26 | 1985-04-09 | Chrysler Corporation | Urethane dies |
| US4608087A (en) * | 1981-06-17 | 1986-08-26 | Shinagawa Refractories Co., Ltd. | Heat-resistant inorganic composition |
| EP0222004A4 (en) * | 1985-05-16 | 1987-10-22 | Handy & Harman | COPPER-ZINC-MANGANESE-NICKEL ALLOYS. |
| US4708626A (en) * | 1985-03-14 | 1987-11-24 | Denki Kagaku Kogyo Kabushiki Kaisha | Mold assembly |
| US4732962A (en) * | 1987-02-18 | 1988-03-22 | General Motors Corporation | High temperature epoxy tooling composition of bisphenol-A epoxy, trifunctional epoxy, anhydride curing agent and an imidazole catalyst |
| US20060027625A1 (en) * | 2001-11-21 | 2006-02-09 | Dana Canada Corporation | Products for use in low temperature fluxless brazing |
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| US20060027625A1 (en) * | 2001-11-21 | 2006-02-09 | Dana Canada Corporation | Products for use in low temperature fluxless brazing |
| US7451906B2 (en) * | 2001-11-21 | 2008-11-18 | Dana Canada Corporation | Products for use in low temperature fluxless brazing |
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