US2138729A - Process of alloying metals with lead - Google Patents
Process of alloying metals with lead Download PDFInfo
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- US2138729A US2138729A US155120A US15512037A US2138729A US 2138729 A US2138729 A US 2138729A US 155120 A US155120 A US 155120A US 15512037 A US15512037 A US 15512037A US 2138729 A US2138729 A US 2138729A
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- 229910052751 metal Inorganic materials 0.000 title description 53
- 239000002184 metal Substances 0.000 title description 53
- 238000000034 method Methods 0.000 title description 34
- 238000005275 alloying Methods 0.000 title description 13
- 150000002739 metals Chemical class 0.000 title description 11
- 230000004907 flux Effects 0.000 description 48
- 150000004820 halides Chemical class 0.000 description 13
- 229910044991 metal oxide Inorganic materials 0.000 description 13
- 239000000203 mixture Substances 0.000 description 13
- NDVLTYZPCACLMA-UHFFFAOYSA-N silver oxide Chemical compound [O-2].[Ag+].[Ag+] NDVLTYZPCACLMA-UHFFFAOYSA-N 0.000 description 10
- 229910000464 lead oxide Inorganic materials 0.000 description 9
- YAFKGUAJYKXPDI-UHFFFAOYSA-J lead tetrafluoride Chemical compound F[Pb](F)(F)F YAFKGUAJYKXPDI-UHFFFAOYSA-J 0.000 description 9
- 230000003647 oxidation Effects 0.000 description 9
- 238000007254 oxidation reaction Methods 0.000 description 9
- YEXPOXQUZXUXJW-UHFFFAOYSA-N oxolead Chemical compound [Pb]=O YEXPOXQUZXUXJW-UHFFFAOYSA-N 0.000 description 9
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 8
- 229910000978 Pb alloy Inorganic materials 0.000 description 7
- 229910052787 antimony Inorganic materials 0.000 description 7
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 description 7
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 7
- 238000006243 chemical reaction Methods 0.000 description 7
- 150000004706 metal oxides Chemical class 0.000 description 7
- 229910052760 oxygen Inorganic materials 0.000 description 7
- 239000001301 oxygen Substances 0.000 description 7
- 229910052714 tellurium Inorganic materials 0.000 description 6
- PORWMNRCUJJQNO-UHFFFAOYSA-N tellurium atom Chemical compound [Te] PORWMNRCUJJQNO-UHFFFAOYSA-N 0.000 description 6
- 229910052785 arsenic Inorganic materials 0.000 description 5
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 description 5
- HWSZZLVAJGOAAY-UHFFFAOYSA-L lead(II) chloride Chemical compound Cl[Pb]Cl HWSZZLVAJGOAAY-UHFFFAOYSA-L 0.000 description 5
- 229910001923 silver oxide Inorganic materials 0.000 description 5
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 4
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 4
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 4
- 229910052802 copper Inorganic materials 0.000 description 4
- 239000010949 copper Substances 0.000 description 4
- 229910052709 silver Inorganic materials 0.000 description 4
- 239000004332 silver Substances 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- 229910000410 antimony oxide Inorganic materials 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 238000011065 in-situ storage Methods 0.000 description 3
- 230000001590 oxidative effect Effects 0.000 description 3
- VTRUBDSFZJNXHI-UHFFFAOYSA-N oxoantimony Chemical compound [Sb]=O VTRUBDSFZJNXHI-UHFFFAOYSA-N 0.000 description 3
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 description 2
- 229910052797 bismuth Inorganic materials 0.000 description 2
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- -1 lead fluoride metal oxide Chemical class 0.000 description 2
- 239000002923 metal particle Substances 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- 229910052711 selenium Inorganic materials 0.000 description 2
- 239000011669 selenium Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- QPLDLSVMHZLSFG-UHFFFAOYSA-N Copper oxide Chemical compound [Cu]=O QPLDLSVMHZLSFG-UHFFFAOYSA-N 0.000 description 1
- 239000005751 Copper oxide Substances 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 229910001245 Sb alloy Inorganic materials 0.000 description 1
- 229910021607 Silver chloride Inorganic materials 0.000 description 1
- 238000003723 Smelting Methods 0.000 description 1
- 229910001128 Sn alloy Inorganic materials 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- IKWTVSLWAPBBKU-UHFFFAOYSA-N a1010_sial Chemical compound O=[As]O[As]=O IKWTVSLWAPBBKU-UHFFFAOYSA-N 0.000 description 1
- 239000004411 aluminium Substances 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 239000002140 antimony alloy Substances 0.000 description 1
- 229960002594 arsenic trioxide Drugs 0.000 description 1
- 229910000416 bismuth oxide Inorganic materials 0.000 description 1
- 229910052793 cadmium Inorganic materials 0.000 description 1
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- WUKWITHWXAAZEY-UHFFFAOYSA-L calcium difluoride Chemical compound [F-].[F-].[Ca+2] WUKWITHWXAAZEY-UHFFFAOYSA-L 0.000 description 1
- 229910001634 calcium fluoride Inorganic materials 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 229910000431 copper oxide Inorganic materials 0.000 description 1
- BERDEBHAJNAUOM-UHFFFAOYSA-N copper(I) oxide Inorganic materials [Cu]O[Cu] BERDEBHAJNAUOM-UHFFFAOYSA-N 0.000 description 1
- 229940112669 cuprous oxide Drugs 0.000 description 1
- KRFJLUBVMFXRPN-UHFFFAOYSA-N cuprous oxide Chemical compound [O-2].[Cu+].[Cu+] KRFJLUBVMFXRPN-UHFFFAOYSA-N 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- TYIXMATWDRGMPF-UHFFFAOYSA-N dibismuth;oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[Bi+3].[Bi+3] TYIXMATWDRGMPF-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000002386 leaching Methods 0.000 description 1
- WABPQHHGFIMREM-NOHWODKXSA-N lead-200 Chemical group [200Pb] WABPQHHGFIMREM-NOHWODKXSA-N 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000013528 metallic particle Substances 0.000 description 1
- 229910000480 nickel oxide Inorganic materials 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- GNRSAWUEBMWBQH-UHFFFAOYSA-N oxonickel Chemical compound [Ni]=O GNRSAWUEBMWBQH-UHFFFAOYSA-N 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 230000036647 reaction Effects 0.000 description 1
- 238000009877 rendering Methods 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- JPJALAQPGMAKDF-UHFFFAOYSA-N selenium dioxide Chemical compound O=[Se]=O JPJALAQPGMAKDF-UHFFFAOYSA-N 0.000 description 1
- HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical compound [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 0.000 description 1
- 239000002893 slag Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 1
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 1
- 229910001887 tin oxide Inorganic materials 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C1/00—Making non-ferrous alloys
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21C—PROCESSING OF PIG-IRON, e.g. REFINING, MANUFACTURE OF WROUGHT-IRON OR STEEL; TREATMENT IN MOLTEN STATE OF FERROUS ALLOYS
- C21C7/00—Treating molten ferrous alloys, e.g. steel, not covered by groups C21C1/00 - C21C5/00
- C21C7/0006—Adding metallic additives
- C21C2007/0012—Lead
Definitions
- One important advantage of using a lead halide flux is that the operation may be carried out at a low temperature of the order of 450- I now flnd that this method is of more general application, and the present invention provides a method of alloying a metal A with lead, which consists in acting upon a bath of molten lead containing a metal B with a flux containing a lead halide and an oxide of the metal A, the metal B being one which, under these conditions, will interact with the oxide and replace the metal A, which will enter the bath of molten lead.
- the lead halides form low melting point mixtures with metallic oxides, and enable the reac tion to be carried out at a low temperature of the order of 450-550 C.
- the metal B may be either lead, or some metal other than tin alloyed with lead. Replacement of tin is excluded from the present invention, since it is already claimed in my application Serial No. 115,629 aforesaid.
- Lithium, sodium, magnesium, aluminium, potassium, calcium, zinc and strontium can readily be replaced in the bath by treatment with a flux containing a suitable metallic oxide. They cannot, however, be introduced into the bath by incorporating them in the flux as oxides.
- the method has the advantage that pure oxides need not be employed, but ores, residues, chemical bye-products etc. may be used.
- an antimony oxide ore may be mixed with the flux, the antimony passing directly into the lead, and being replaced by a metal B present in the bath.
- the lead alloy is melted in a kettle and heated to about 550 C.
- the flux with the whole or a part of the metal oxide A is then added and the whole forms a fluid layer on top of the metal.
- Stirring is then commenced and is effected by the usual means until the reaction is finished, the balance, if any, of the metal oxide A being meanwhile added.
- it is preferable to make more than one flux addition and this is specially so where selective removal of a certain metal from the bath is aimed at.
- reaction be carried out to a definite degree, such as in the preferential removal of a certain metal, it may be an advantage to work in a non-oxidizing atmosphere thus enabling the amount of oxygen taking part in the reaction to be controlled by the quantity of metal oxide added.
- arsenious oxide 75 parts of arsenious oxide, 150 parts of lead chloride and 1000 parts of molten lead containing 5% of antimony were stirred for fifteen minutes.
- arsenic replaced both lead and antimony in the bath, which was found on final analysis to contain 4.4% of antimony and 2.86% of arsenic.
- oxides of metals A are quoted it must be understood that the process is not confined to the primary addition of the oxides of metal A as such.
- oxides of metal A may be formed in situ by a variety of methods, e. g., carbonates or nitrates decomposable by heating provide a ready source of oxides, compounds or mixtures of lead oxide with other metallic oxides, e. g., lead antimoniate act similarly.
- processes of double decomposition are applicable, e. g., a mixture of silver chloride and lead oxide heated together on a bath of molten lead give rise to silver oxide and lead chloride, the silver oxide being then available to act as the oxide of metal A.
- Their application, by the method according to the invention, to the manufacture of lead alloys provides a useful method for the treatment of residues, chemical bye-products etc. as previously mentioned.
- the lead fluoride metal oxide fluxes may, after removal from the bath, he smelted direct with carbon and lime, the fluorine passing into the slag as calcium fluoride.
- the flux may be mixed with a proportion of carbon sumcient only to reduce a part of the metal oxides and the residual fiux now enriched in lead fluoride can be used again.
- the lead chloride in the case of lead chloride metal oxide fluxes, can be separated by volitilization from the metal oxide, or by leaching with water.
- a process of alloying metals with lead which comprises the steps of treating a bath of molten lead with a flux, consisting of a mixture of a lead halide and an oxide of a metal having, under the alloyed with conditions of the process, a less affinity for oxygen than lead, thereby effecting oxidation of a portion of the lead and replacement thereof in the bath by the said metal and removing the lead oxide so formed by separating the flux from the bath.
- a flux consisting of a mixture of a lead halide and an oxide of a metal having, under the alloyed with conditions of the process, a less affinity for oxygen than lead
- a process of alloying copper with lead which comprises the steps of treating a bath of molten lead with a flux, consisting of a mixture of a lead halide and copper oxide, thereby effecting oxidation of a portion of the lead and replacement thereof in the bath by copper, and removing the lead oxide so formed by separating the flux from the bath.
- a process of alloying tellurium with lead which comprises the steps of treating a bath of molten lead with a flux, consisting of a mixture of a lead halide and tellurium oxide, thereby effecting oxidation of a portion of the lead and replacement thereof in the bath by tellurium, and removing the lead oxide so formed by separating 1 the flux from the bath.
- a process of alloying silver with lead which comprises the steps of treating a bath of molten lead with a flux, consisting of a mixture of a lead halide and silver oxide, thereby effecting oxidation of a portion of the lead and replacement thereof in the bath by silver, and removing the lead oxide so formed by separating the flux from the bath.
- a process of alloying metals with lead which comprises the steps of treating a bath of molten lead with a flux, consisting of a mixture of a lead chloride and an oxide of a metal having, under the conditions of the process, a less aflinity for oxygen than lead, thereby effecting oxidation of a portion of the lead and replacement thereof in the bath by the said metal and removing the lead oxide so formed by separating the flux from the bath.
- a flux consisting of a mixture of a lead chloride and an oxide of a metal having, under the conditions of the process, a less aflinity for oxygen than lead
- a process of alloying metals with lead which comprises the steps of treating a bath of molten lead with a flux, consisting of a mixture of a lead fluoride and an oxide of a metal having, under the conditions of the process, a less afllnity for oxygen than lead, thereby effecting oxidation of a portion of the lead and replacement thereof in the bath by the said metal and removing the lead oxide so formed by separating the flux from the bath.
- a process of alloying metals with lead which comprises the steps of treating a bath of a molten lead alloy with a flux, consisting of a mixture of a lead halide and an oxide of a metal having, under the conditions of the process, a less aflinity for oxygen than a metal other than tin in the bath, thereby effecting oxidation of said metal in the bath and its replacement by the metal obtained by the reduction of the oxide in the flux and separating the flux from the bath.
- a process of alloying arsenic with lead which comprises the steps of treating a bath of a molten lead-antimony alloy with a flux consisting of a mixture of a lead halide and arsenious ox-- r ide, thereby efiecting oxidation of a portion of the lead and antimony, and replacement thereof 15 in the bath by arsenic, and removing the lead om'de and antimony oxide so formed by separating the flux from the bath.
- a process of alloying metals with lead which comprises the steps of treating a oath of a molten lead alloy with a flux, consisting of a mixture of a lead halide and an oxide of a metal having, under the conditions of the process, a less afiinity for oxygen than a metal other than tin in the bath, thereby effecting om'dation of said metal in the bath and its replacement by the metal obtained by the reduction of the oxide in the flux, separating the flux from the bath, and treating the flux with a quantity of carbon snfiicient to reduce a part only of the metallic oxides therein, so rendering the flux suitable forre-use.
- a process of alloying metals with lead which comprises the steps of treating a bath of a molten lead alloy with a flux, consisting of a mixture of a lead halide and an oxide of a metal having, under the conditions of the process, a less afilnity for oxygen than a metal other than tin in the bath, thereby effecting oxidation of said metal in the bath and its replacement by the metal obtained by the reduction of the oxide in the flux, separating the flux from the bath, and smelting the flux direct to reduce the oxides therein to metal.
- a flux consisting of a mixture of a lead halide and an oxide of a metal having, under the conditions of the process, a less afilnity for oxygen than a metal other than tin in the bath, thereby effecting oxidation of said metal in the bath and its replacement by the metal obtained by the reduction of the oxide in the flux, separating the flux from the bath, and smelting the flux direct to reduce the oxides therein to metal.
- a process of recovering metal particles from oxide residues which consistsin treating a bath containing molten lead with a flux containing the residue and a lead halide, thereby efiecting union between the metal particles and the ba h, 20
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Manufacture And Refinement Of Metals (AREA)
Description
Patented Nov. 29, 1938 UNITED STATES PATENT. OFFICE rnoonss or ALLOYING METALS WITH No Drawing.
Application July 22, 1937, Serial No. 155,120. In Great Britain August 8, 1936 17 Claims.
In my United States application Serial No. 115,629, filed December 12th, 1936, which has issued as Patent 2,097,560 dated Nov. 2, 1937, I have described a method of preparing alloys of lead by adding to a bath of a molten alloy of lead and tin a lead halide flux containing a reducible compound (e. g. an oxide) of the metal to be alloyed with the lead. Under these conditions the tin replaces the metal present in the reducible compound, tin oxide separating with the flux and the other metal replacing tin in the bath. One important advantage of using a lead halide flux is that the operation may be carried out at a low temperature of the order of 450- I now flnd that this method is of more general application, and the present invention provides a method of alloying a metal A with lead, which consists in acting upon a bath of molten lead containing a metal B with a flux containing a lead halide and an oxide of the metal A, the metal B being one which, under these conditions, will interact with the oxide and replace the metal A, which will enter the bath of molten lead.
The lead halides form low melting point mixtures with metallic oxides, and enable the reac tion to be carried out at a low temperature of the order of 450-550 C.
The metal B may be either lead, or some metal other than tin alloyed with lead. Replacement of tin is excluded from the present invention, since it is already claimed in my application Serial No. 115,629 aforesaid.
I have found that copper, selenium, silver, tellurium and bismuth can be caused to replace lead or other metals in the bath by incorporating them as oxides in the flux. They cannot, however, be removed from the bath by the method herein described.
Lithium, sodium, magnesium, aluminium, potassium, calcium, zinc and strontium can readily be replaced in the bath by treatment with a flux containing a suitable metallic oxide. They cannot, however, be introduced into the bath by incorporating them in the flux as oxides.
In the case of nickel, cadmium, arsenic and antimony, the reaction is reversible and these metals can be extracted from or introduced into the bath.
The method has the advantage that pure oxides need not be employed, but ores, residues, chemical bye-products etc. may be used. Thus, for example, an antimony oxide ore may be mixed with the flux, the antimony passing directly into the lead, and being replaced by a metal B present in the bath.
When oxide residues are employed which con- 1 tain metallic particles, these in contact with the fluid flux melt and joint the metal bath.
Some examples of how the invention can be carried into effect will now be given.
In each of the examples quoted below the lead alloy is melted in a kettle and heated to about 550 C. The flux with the whole or a part of the metal oxide A is then added and the whole forms a fluid layer on top of the metal. Stirring is then commenced and is effected by the usual means until the reaction is finished, the balance, if any, of the metal oxide A being meanwhile added. In some cases it is preferable to make more than one flux addition and this is specially so where selective removal of a certain metal from the bath is aimed at.
In certain circumstances where it is desired that the reaction be carried out to a definite degree, such as in the preferential removal of a certain metal, it may be an advantage to work in a non-oxidizing atmosphere thus enabling the amount of oxygen taking part in the reaction to be controlled by the quantity of metal oxide added.
5 parts of silver oxide were mixed with 50 parts of lead fluoride and stirred into 1000 parts' of molten lead for fifteen minutes. The metal upon analysis contained 46% of the silver added as oxide, lead oxide replacing the reduced silver oxide in the flux. Similar results were obtained using lead chloride as a flux.
III
5 parts of tellurium oxide were treated in a manner similar to the above and of the tellurium added as crude replaced lead in the bath using a lead fluoride flux.
III
5 parts of bismuth oxide, 50 parts of lead fluoride and 1000 parts of molten lead were stirred for fifteen minutes, when 99% of the contained bismuth replaced lead in the metal bath.
5 parts of nickel oxide, 50 parts of lead fluoride and 1000 parts of molten lead were stirred together for fifteen minutes after which 10% of the nickel added was found to be the lead.
Using lad fluoride as a flux 1000 parts of molten lead were stirred for fifteen minutes with 100 parts of lead fluoride and 200 parts of antimony oxide after which of the antimony was found to have alloyed with the metal.
VII
5 parts of cuprous oxide, 50 parts lead fluoride and 1000 parts of molten lead werestirred together for fifteen minutes after which it was found that 72% of the copper added as oxide was alloyed with the bath.
VIII
5 parts of selenium oxide, 50 parts of lead fluoride and 1000 parts of molten lead were stirred for fifteen minutes after which it was found that 16% of the selenium added as oxide had replaced lead and become alloyed in the bath.
75 parts of arsenious oxide, 150 parts of lead chloride and 1000 parts of molten lead containing 5% of antimony were stirred for fifteen minutes. In this example arsenic replaced both lead and antimony in the bath, which was found on final analysis to contain 4.4% of antimony and 2.86% of arsenic.
Although in .the foregoing examples the oxides of metals A are quoted it must be understood that the process is not confined to the primary addition of the oxides of metal A as such. Thus oxides of metal A may be formed in situ by a variety of methods, e. g., carbonates or nitrates decomposable by heating provide a ready source of oxides, compounds or mixtures of lead oxide with other metallic oxides, e. g., lead antimoniate act similarly. Also processes of double decomposition are applicable, e. g., a mixture of silver chloride and lead oxide heated together on a bath of molten lead give rise to silver oxide and lead chloride, the silver oxide being then available to act as the oxide of metal A. Their application, by the method according to the invention, to the manufacture of lead alloys provides a useful method for the treatment of residues, chemical bye-products etc. as previously mentioned.
In the case of the lead fluoride metal oxide fluxes, these may, after removal from the bath, he smelted direct with carbon and lime, the fluorine passing into the slag as calcium fluoride.
Alternatively, the flux may be mixed with a proportion of carbon sumcient only to reduce a part of the metal oxides and the residual fiux now enriched in lead fluoride can be used again.
In the case of lead chloride metal oxide fluxes, the lead chloride can be separated by volitilization from the metal oxide, or by leaching with water.
What I claim as my invention and desire to secure by Letters Patent is:
1. A process of alloying metals with lead, which comprises the steps of treating a bath of molten lead with a flux, consisting of a mixture of a lead halide and an oxide of a metal having, under the alloyed with conditions of the process, a less affinity for oxygen than lead, thereby effecting oxidation of a portion of the lead and replacement thereof in the bath by the said metal and removing the lead oxide so formed by separating the flux from the bath.
2. A process of alloying copper with lead, which comprises the steps of treating a bath of molten lead with a flux, consisting of a mixture of a lead halide and copper oxide, thereby effecting oxidation of a portion of the lead and replacement thereof in the bath by copper, and removing the lead oxide so formed by separating the flux from the bath.
3. A process of alloying tellurium with lead, which comprises the steps of treating a bath of molten lead with a flux, consisting of a mixture of a lead halide and tellurium oxide, thereby effecting oxidation of a portion of the lead and replacement thereof in the bath by tellurium, and removing the lead oxide so formed by separating 1 the flux from the bath.
4. A process of alloying silver with lead, which comprises the steps of treating a bath of molten lead with a flux, consisting of a mixture of a lead halide and silver oxide, thereby effecting oxidation of a portion of the lead and replacement thereof in the bath by silver, and removing the lead oxide so formed by separating the flux from the bath.
5. A process according to claim 1, in which the reaction is carried out in a non-oxidizing atmosphere.
6. A process according to claim 1, in which the oxide of the metal to be alloyed with the lead is formed in situ.
'7. A process according to claim 1, in which the metal oxide is introduced into the flux in the form of an ore or residue.
8. A process of alloying metals with lead, which comprises the steps of treating a bath of molten lead with a flux, consisting of a mixture of a lead chloride and an oxide of a metal having, under the conditions of the process, a less aflinity for oxygen than lead, thereby effecting oxidation of a portion of the lead and replacement thereof in the bath by the said metal and removing the lead oxide so formed by separating the flux from the bath.
9. A process of alloying metals with lead, which comprises the steps of treating a bath of molten lead with a flux, consisting of a mixture of a lead fluoride and an oxide of a metal having, under the conditions of the process, a less afllnity for oxygen than lead, thereby effecting oxidation of a portion of the lead and replacement thereof in the bath by the said metal and removing the lead oxide so formed by separating the flux from the bath. V
10. A process of alloying metals with lead, which comprises the steps of treating a bath of a molten lead alloy with a flux, consisting of a mixture of a lead halide and an oxide of a metal having, under the conditions of the process, a less aflinity for oxygen than a metal other than tin in the bath, thereby effecting oxidation of said metal in the bath and its replacement by the metal obtained by the reduction of the oxide in the flux and separating the flux from the bath.
11. A process of alloying arsenic with lead, which comprises the steps of treating a bath of a molten lead-antimony alloy with a flux consisting of a mixture of a lead halide and arsenious ox-- r ide, thereby efiecting oxidation of a portion of the lead and antimony, and replacement thereof 15 in the bath by arsenic, and removing the lead om'de and antimony oxide so formed by separating the flux from the bath.
12. A process according to claim 10, in which the reaction is carried out in a non-oxidizing atmosphere.
13. A process according to claim 10, in which the oxide of the metal to be alloyed with the lead is formed in situ.
14. A process according to claim 10, in which the metal oxide is introduced into the flux in the form of an ore or residue.
15. A process of alloying metals with lead, which comprises the steps of treating a oath of a molten lead alloy with a flux, consisting of a mixture of a lead halide and an oxide of a metal having, under the conditions of the process, a less afiinity for oxygen than a metal other than tin in the bath, thereby effecting om'dation of said metal in the bath and its replacement by the metal obtained by the reduction of the oxide in the flux, separating the flux from the bath, and treating the flux with a quantity of carbon snfiicient to reduce a part only of the metallic oxides therein, so rendering the flux suitable forre-use.
16. A process of alloying metals with lead, which comprises the steps of treating a bath of a molten lead alloy with a flux, consisting of a mixture of a lead halide and an oxide of a metal having, under the conditions of the process, a less afilnity for oxygen than a metal other than tin in the bath, thereby effecting oxidation of said metal in the bath and its replacement by the metal obtained by the reduction of the oxide in the flux, separating the flux from the bath, and smelting the flux direct to reduce the oxides therein to metal.
17. A process of recovering metal particles from oxide residues, which consistsin treating a bath containing molten lead with a flux containing the residue and a lead halide, thereby efiecting union between the metal particles and the ba h, 20
and thereafter separating the flux from the bath.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB2138729X | 1936-08-08 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2138729A true US2138729A (en) | 1938-11-29 |
Family
ID=10899524
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US155120A Expired - Lifetime US2138729A (en) | 1936-08-08 | 1937-07-22 | Process of alloying metals with lead |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2138729A (en) |
-
1937
- 1937-07-22 US US155120A patent/US2138729A/en not_active Expired - Lifetime
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