USRE21690E - Preparation of contact masses from - Google Patents
Preparation of contact masses from Download PDFInfo
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- USRE21690E USRE21690E US21690DE USRE21690E US RE21690 E USRE21690 E US RE21690E US 21690D E US21690D E US 21690DE US RE21690 E USRE21690 E US RE21690E
- Authority
- US
- United States
- Prior art keywords
- gel
- pieces
- drying
- dried
- wet
- 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
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- 238000002360 preparation method Methods 0.000 title description 7
- 239000000499 gel Substances 0.000 description 98
- 239000000203 mixture Substances 0.000 description 43
- 239000000463 material Substances 0.000 description 39
- 238000001035 drying Methods 0.000 description 37
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 27
- 239000002245 particle Substances 0.000 description 25
- 239000003054 catalyst Substances 0.000 description 20
- 238000000034 method Methods 0.000 description 17
- 238000000465 moulding Methods 0.000 description 14
- 239000011240 wet gel Substances 0.000 description 14
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 13
- 230000000274 adsorptive effect Effects 0.000 description 13
- 238000002156 mixing Methods 0.000 description 13
- 230000008569 process Effects 0.000 description 13
- 239000000126 substance Substances 0.000 description 13
- 239000008188 pellet Substances 0.000 description 10
- 239000012634 fragment Substances 0.000 description 9
- 238000012360 testing method Methods 0.000 description 9
- 238000004519 manufacturing process Methods 0.000 description 7
- 239000002253 acid Substances 0.000 description 6
- 239000011230 binding agent Substances 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 6
- 239000004115 Sodium Silicate Substances 0.000 description 5
- 238000010438 heat treatment Methods 0.000 description 5
- 238000007654 immersion Methods 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 229910052911 sodium silicate Inorganic materials 0.000 description 5
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 4
- 238000009835 boiling Methods 0.000 description 4
- 239000000741 silica gel Substances 0.000 description 4
- 229910002027 silica gel Inorganic materials 0.000 description 4
- 238000011282 treatment Methods 0.000 description 4
- 229910052782 aluminium Inorganic materials 0.000 description 3
- 230000003197 catalytic effect Effects 0.000 description 3
- 238000001125 extrusion Methods 0.000 description 3
- 239000012213 gelatinous substance Substances 0.000 description 3
- 230000001050 lubricating effect Effects 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 150000002739 metals Chemical class 0.000 description 3
- -1 tungstic Chemical class 0.000 description 3
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 229910017052 cobalt Inorganic materials 0.000 description 2
- 239000010941 cobalt Substances 0.000 description 2
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- 239000012065 filter cake Substances 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 238000000227 grinding Methods 0.000 description 2
- 239000008241 heterogeneous mixture Substances 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 150000004679 hydroxides Chemical class 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 229910052749 magnesium Inorganic materials 0.000 description 2
- 239000011777 magnesium Substances 0.000 description 2
- 235000001055 magnesium Nutrition 0.000 description 2
- 229940091250 magnesium supplement Drugs 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- 235000010603 pastilles Nutrition 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 238000012958 reprocessing Methods 0.000 description 2
- 230000000717 retained effect Effects 0.000 description 2
- 150000004760 silicates Chemical class 0.000 description 2
- 238000005245 sintering Methods 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 229910052684 Cerium Inorganic materials 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- 244000228957 Ferula foetida Species 0.000 description 1
- 239000004902 Softening Agent Substances 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- DOIXGGGORNAJAT-UHFFFAOYSA-M [NH4+].[Ni+].[O-]S([O-])(=O)=O Chemical compound [NH4+].[Ni+].[O-]S([O-])(=O)=O DOIXGGGORNAJAT-UHFFFAOYSA-M 0.000 description 1
- YKTSYUJCYHOUJP-UHFFFAOYSA-N [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] Chemical compound [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] YKTSYUJCYHOUJP-UHFFFAOYSA-N 0.000 description 1
- 150000004645 aluminates Chemical class 0.000 description 1
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 description 1
- DNEHKUCSURWDGO-UHFFFAOYSA-N aluminum sodium Chemical compound [Na].[Al] DNEHKUCSURWDGO-UHFFFAOYSA-N 0.000 description 1
- ANBBXQWFNXMHLD-UHFFFAOYSA-N aluminum;sodium;oxygen(2-) Chemical compound [O-2].[O-2].[Na+].[Al+3] ANBBXQWFNXMHLD-UHFFFAOYSA-N 0.000 description 1
- LCQXXBOSCBRNNT-UHFFFAOYSA-K ammonium aluminium sulfate Chemical compound [NH4+].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O LCQXXBOSCBRNNT-UHFFFAOYSA-K 0.000 description 1
- 210000000988 bone and bone Anatomy 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 239000004568 cement Substances 0.000 description 1
- ZMIGMASIKSOYAM-UHFFFAOYSA-N cerium Chemical compound [Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce] ZMIGMASIKSOYAM-UHFFFAOYSA-N 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 238000005352 clarification Methods 0.000 description 1
- 238000003776 cleavage reaction Methods 0.000 description 1
- 230000001427 coherent effect Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000004042 decolorization Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 238000011038 discontinuous diafiltration by volume reduction Methods 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000010981 drying operation Methods 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 239000002360 explosive Substances 0.000 description 1
- 210000003414 extremity Anatomy 0.000 description 1
- 239000007863 gel particle Substances 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 238000013007 heat curing Methods 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 210000001699 lower leg Anatomy 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 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 description 1
- 238000012856 packing Methods 0.000 description 1
- 229920000136 polysorbate Polymers 0.000 description 1
- 235000019353 potassium silicate Nutrition 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000005057 refrigeration Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- 238000012216 screening Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000010008 shearing Methods 0.000 description 1
- 229910001388 sodium aluminate Inorganic materials 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 125000005402 stannate group Chemical group 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 238000005496 tempering Methods 0.000 description 1
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 239000010937 tungsten Substances 0.000 description 1
- LSGOVYNHVSXFFJ-UHFFFAOYSA-N vanadate(3-) Chemical class [O-][V]([O-])([O-])=O LSGOVYNHVSXFFJ-UHFFFAOYSA-N 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
- B01J20/02—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material
- B01J20/06—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material comprising oxides or hydroxides of metals not provided for in group B01J20/04
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
- B01J37/0009—Use of binding agents; Moulding; Pressing; Powdering; Granulating; Addition of materials ameliorating the mechanical properties of the product catalyst
Definitions
- gels or gel-like materials having properties which make them suitable for use as contact masses includef-other silicious materials, such for example, assimple silicates of many metals as of aluminum, iron, zinc, copper, vanadium, mag nesium, calcium, tungsten, nickel, manganese, cobalt, cerium; poly-silicates of alumina and other metals, some of which have base exchanging or zeolitic properties; salts containing negative metallic radicals and which can precipitate in gel form, as exemplified by certain alluminates, vanadates, tungstates, stannates and titanates; hydroxides which can be obtained as gels such as the hydroxides of iron, aluminum, chromium, copper, cobalt, nickel, etc.; certain acids such as tungstic, stannic and titanic acids; and mixtures or compounds of the above classes oi substances.
- assimple silicates of many metals as of aluminum, iron, zinc, copper, vanadium, mag nesium,
- the contact material in pieces of uniform size and shape. This can best be efiected by a molding operation.
- previous attempts to mold wet gel directly have often resulted in complete failure, and when the molding opera tion was at all possible the molded pieces were no better in quality than, and often inferior to, fragmentary pieces produced by the above described method oi! forming a solid cake and then crushing it.
- the binder diluted or modified the contact mass, and, in numerous instances, the resulting pieces were decidedly inferior in quality. It has been proposed also to use a binder which could be converted into an active form by treatment of the molded pieces. was proposed as a binding material for silica gel. The molded pieces were to be treated by acid so as to convert the sodium silicate into silica gel. This conversion in many instances was incomplete or required excessive lengths of time and amounts of acid. Furthermore, the treatment was apt to be detrimental to the physical and/or chemical structure of the contact mass. In every case processes designed for reclamation of fines involved a second handling and reprocessing of a substantial proportion of the dried gel. In many instances, expensive equipment and/or additional material including chemical reagents were required.
- One object of the present invention is to provide a simple and efilcient method of preparing contact masses from sols, gels or gel-like materials. Another object is to produce from the above materials contact masses in any desired size and shape and in stable form. Another object is-to transform such materials into molded pieces of improved porosity and having increased amounts of readily available contact surface. Another object is to produce such masses without the use of extraneous binding materials. Still another objectis to avoid the production of fines or waste material of depreciated value. Still other objects will be apparent from the detailed discussion which follows.
- the invention involves a method for producing from a gel a heterogeneous plastic mass which will not shrink to any substantial extent when dried, and which hardens into a coherent body having high mechanical stability.
- This plastic mass is still, but readily workable, and resembles in many respects'batches of potters and brickmakers molding mixtures. It is peculiarly adapted to forming or molding operations including extrusion, pelletting, etc.
- the essential steps for the preparation of the unshrinkable plastic mass are as follows:
- a gel ofthe desired composition is prepared and may then be washed in known manner, with or without removal of excess liquid;
- step (d) The dried and comminuted portion is then blended with gelatinous material remaining from step (b) to produce a plastic mass of the proper Prior to er during the subsequent forming operation the plastic mass is preferably subjected to substantial pressure in order to eflect compactingof the preshrunk particles and even distribution of'a thin layer of tbewet partof the gel between and around these particles.
- substantial pressure for example, sodium silicate greater strength with finer division.
- sufi'icient pressure is exerted on the mass when it is forced through an extrusion die or when it is compacted or compressed in the prep- :on drying of the formed pieces, firmly cements dried molded pieces are further characterized by having high physical or mechanical stability, as evidenced by high crus'hing, tensile and shearing strengths and by resistance to disintegration when wet by or immersed in liquids.
- the most suitable ratio of preshrunk particles to undried material in the plastic mixture varies with the characteristics of the gel and can easily be determined for each gel by simple experi- 3 mer ts.
- the 'best plastic mixtures are obtained by utilizing dried gel considerably in excess of wet gel, good results being obtained when the ratio of gel which is preshrunk to unmodified gel lies within or above the range of 1:1 to 5.7:1. When a complete batch of gel is utilized this range corresponds to effecting preshrinkage of to 85% of the original material. For silicious materials" good results may be obtained when the ratio iiesa'bove 1.5: 1 as up to 421, or at least to. 80% of the gel-is pre- -r shrunk when a given batch is completely used up.
- Moderate temperatures are preferably employed in the preshrinking step. Temperatures which cause sintering of the starting material or removal of excessive amounts of any water of composition from the gel sometimes tend to impair the mechanical stability of the formed pieces. Good results are usually obtained when drying temperatures under 400 F. are used, such, for 5 example, as 180 to 250 F.
- the strength of the finished piecesof contact mass is to some extent dependent upon the size of the finely divided preshrunk material, the tendency being toward Suitable particle sizes are 60 mesh or liner, and preferably 100 mesh or finer, as up to 400 mesh.
- the gels may be mixed prior to the preshrinking stepper all or a predetermined proportionof one. or more of the gels may be preshrunk, the re-, maining material serving as the wet portion of.
- plastic mixture It is sometimes desirable to include non-sei-nke materials in a contact mass, as for example, finely divided metals or metallic compounds. Such material can be mixed with the original gel, but is preferably added to that portion-of the gel which has been the process of being preshrunk.
- the step of combining the preshrunk and wet fractions of the gel can be effected inany type of apparatus capable of making a good mixture.
- the molded pieces can bedried at any temperature that is consistent with maintenance of the physical and/or chemical stability of the gellike substance or substances comprising the mass.
- drying temperatures within the range specified for the preshrinking step produce pieces having satisfactory strength.
- in order to provide an exceptionally strong bond between the preshrunk and wet portion of the gel it is desirable to use somewhat higher temperatures as up to 600 F. or 700 F. or up to 1000 F. but below the temperature at which the physical or chemical structure of the mass is destroyed as through sintering or elimination of water of combination.
- drying temperatures which cause change in the structure of the mass can be e plo e
- the following examples provide specific illustrations of the invention:
- Example 1 An aluminum silicate gel was made by the interaction between sodium silicate and ammonium aluminum sulphate. The precipitate was washed and excess water removed as well as possible in a vacuum filter. Approximately 75% of the resulting filter cake was substantially completely dried in a current of air for about hours at about 220 F. and the dried material ground to about 150 mesh. The dried and ground gel was mixed with the remaining portion ofthe wet gel to form a plastic mass which was extruded and cut-to produce cylindrical pieces of about 2 mm. diameter and 4 mm. in length. These were dried at about 220 1'. The dried pieces were strong, porous and highly adsorptive.
- the individual pieces were capable of resisting concentrated loads as high as 600 grams applied through a knife edge perpendicular to the axis of the cylinder and were capable of absorbingand retaining 95 to 100% of their weight of water.
- 600 1 When heated to 600 1".these cylinders resisted concentrated loads of about 900 grams under a knife edge and had about the same absorptive capacity. Even after heating to 600' It, the pieces had substantially the same diameter as wheni'reshly extruded.
- Example 2 In order to determine in detail the advantages of the present invention over the former conventional methods of preparing contact masses from gels, a batch of silica gel, which was precipitated and washed in conventional manner, was subjected to different treatments.
- a portion of the batch was dried at temperatures in the range of 180 to 220 F., duringwhich step the gel shrunk to about 40% of its original volume.
- the dried material was crushed to produce fragments which were screened to segregate pieces having a size of 4 to 8 mesh. These pieces were then heated to about 700 F. and were examined.
- the individual fragments were dense and possessed definite cleavage planes.
- the strengths of these fragments' were not uniform, some of them splitting under conce'ntrated loads as low as 50 grams. When im mersed in water they rapidly disintegrated to small grains, none of which was larger than about 16 mesh.
- the disintegrated fragments were capable of absorbing about 65% of water by weight.
- A'plastic mixture was prepared from this remainder by drying and grinding approximately 80% of it, substantially as described in Example 1, and then mixing the dried and ground part with the remaining portion of wet gel.
- the remaining portion of the plastic mixture was not molded but was compressed under a pressure of about 1500-pounds persquare inch and was then dried at temperatures which were slowly increased to about 600 F. in substantially the same manner as the first portion of the plastic mass. Practically no shrinkage of the mass took place during the drying step.
- the dried mass was broken into fragments, all of which were resistant to disintegration upon immersion in boiling water, even when they were large enough to be retained on a 2 mesh screen. They could absorb about 100% of water by weight.
- the fragmented pieces were then screened to segregate pieces having a size of 4 to 8 mesh.
- Example 4 A blend of magnesium and aluminum silicates was made by reacting aluminum alum and magnesium sulphate with water-glass. Approximately 75% of the resulting gel was dried and ground substantially as described in Example 1 and mixed, with the remaining portion of the wet gel to produce a plastic mixture. From this mixture molded pellets were produced by extrusion through a die providing 2 mm. openings. The pellets were dried at temperatures within the range 01 400 to 600 F. Again no appreciable shrinkage of the pellets took place. They were capable of resisting concentrated loads of approximately 950 grams and could absorb about 85% water by weight.
- Example 5 A zeolitic polysilicate capable of use asa water treating agent was prepared by the reaction between sodium aluminate and sodium silicate. Approximately 75% of the resulting sodium aluminum silicate gel. was preshrunk and ground to 100 mesh and then combined with the re- 1 mainlng wet portion of the gel substantially as described in Example 1. mixture wasmolded into pellets. After drying at temperatures in the range of 180 to 220 F.,:the pellets resisted concentrated loads of about 1000 grams and could absorb approximately 75% water by weight. When immersed in boiling water they did not disintegrate, nor did fragmented pieces prepared by drying and breaking an unextruded portion oi the plastic mixture. Both the extruded and fragmented forms were capable of shipment in a-substantlally bone dry state.
- venadyl aluminate and stannic acid may be selected as representative of materials at or near the extremities of the range of ratios of the part to be preshrunk and comminuted to. the part retained in wet form. Strong. highly adsorptive molded pieces are produced from vanadyl aluminate when at least 50% of the original gel is dried and ground. In the case of stannic acid a good plastic non-shrinkable mixture is made when approximately 85% or more of the gel is preshrunk.
- knife edge When the term knife edge" is used herein and.
- the process of producing a substantially unshrinkable plastic mixture therefrom comprising providingtwo unequal portions of wet gel or gel-like material, the amount of one of said portions being at least three times the amount of, the other, drying the larger of said portions to effect substantially complete shrinkage of the same and or gel-like material, the amount of one of said portions being at least three times the amount of the other, drying the larger of said portions to eifect substantially complete shrinkage of the same, mixing the two portions, and molding the resulting plastic mixture under substantial pressure.
- An adsorptive preformed unit valuable for use as catalyst or catalyst support consisting of a hard heterogeneous aggregate of finely divided prehardened particles of' synthetic inorganic gel bonded together by a minor quantity of synthetic inorganic gel uniformly distributed among said particles, a cylindrical test piece of the aggregate having a diameter of about 2 mm. being strong enough to support concentrated load of at least 700 grams applied through a knife edge across its axis.
- An adsorptive molded unit of predetermined size and shape suitable for use as catalyst or catalyst support consisting oi 100 mesh or finer hardened synthetic inorganic gel particles bonded together in a dry, hard, tough, heterogeneous aggregate by a minor quantity of synthetic inorganic gel uniformly distributed throughout the aggregate and between said particles, said unit having adsorptive capacity for water of at least 75% water by weight and being resistant to disintegration upon immersion in or saturation with water, the resistance of said unit to mechanical ganic gel uniformly distributed among and be-- tween said particles'to form a heterogeneous aggregate, a cylindrical test piece of which having a diameter of about 2 mm. will support a concentrated load of at least 900 grams applied through a knife edge across its axis.
- a highly adsorptive molded unit valuable for use as catalyst or catalyst support consisting of plural oxide synthetic inorganic gel, said unit being composed of prehardened particles of synthetic gel of 60 mesh size or smaller bonded together in a porous, tough, hard heterogeneous aggregate by a further quantity of the same gel uniformly distributed among said particles by mixture therewith and limited to such minor amount that test pieces of the aggregate in the form of cylinders of about 2 mm. diameter will support at least 900 grams concentrated loadapplied through a knife edge across its axis. 1.
- a rigid heterogeneous preformed aggregate adapted for use as catalyst or catalyst support I thetic inorganic gel uniformly distributed between and around said particles and cementing the latter together in a hard, tough, porous body. a cylindrical test piece of which having a diameter of about 2 mm. will support a least 900 grams ugh a knife edge across its axis. 18.
- An adsorptive unit valuable for use as catalyst or catalyst support comprising a preformed body of 2 to 4 mm.
- diameter consisting of finely divided particles of synthetic inorganic gel bonded together in aheterogeneous dry, hard aggregate by a further but minor quantity of synthetic inorganic gel which had been mixed in the wet state with said .particles,said body .having such high resistance to mechanical stress that a cylindrical test piece of the dry, hard aggregate having a diameter of about 2 mm. will support at least I00 grams concentrated load applied through a knife edge across its axis.
- a molded, rigid heterogeneous aggregate suitable for use as catalyst or catalyst support consisting oi'iinely divided particles of a plural oxide silicious gel bonded together by a further quantity of silicious gel, which had been uniformly distributed in wet state between and around said particles and subsequently hardened, the gel in wet state being limited to such minor amount that the hardened aggregate is resistant to disintegration upon immersion in or saturation with water and has such resistance to mechanical stress that a cylindrical specimen of the aggregate having a diameter'of about 2 mm. will support at least 900 grams concentrated load applied through a knife edge across its axis.
- a cylindrical specimen of the aggregate having a lubricating and binding material containing v synthetic inorganic gelatinous substance as the sole binding agent, proportioning said gel and said material so that the resulting heterogeneous mixture contains only a minor quantity of said substance and is stii! and workable but willnot shrink to substantial 'extent upon drying, moldingsaid mixture into' pieces of predetermined size and shape, and heating the molded pieces to dry them and to yield a product, cylindrical test pieces of which of about 2 mm. diameter will support concentrated loads of' at least 700 grams applied through a knife edge perpendicular to their axes.
- a contact mass valuable for use as catalyst or catalyst support consisting wholly of the-same precipitated inorganic gel and comprising a dry, hard molded unit having high adsorptive ca-' pacity for water and being resistant to disinte gration upon immersion in or saturation with water, said unit having a porous heterogeneous structure of strongly bonded discrete particles of dried gel of a fineness of at least 100 mesh and having such strength that a cylindrical test specimen of about 2 mm.
- the diameter will support at least 700 grams concentrated load applied across its axis, said unit being identical with the product produced by reducing said gel to prehardened and preshrunk finely divided condition, incorporating with the finely divided gel a lubricating and binding material containing synthetic inorganic gelatinous substance as the sole binding agent, proportioning said gel and said material so that the resulting heterogeneous mix- I ture contains only a minor quantity of said substance and is still and workable but will not shrink to substantial extent upon drying, molding the mixture into pieces of predetermined size and shape, and heating the molded pieces to dry and harden them.
- a contact mass valuable for use as a catalyst or catalyst support consisting wholly oi the same precipitated silica-alumina gel and comprising a dry, hard molded unit having high adsorptive capacity for water and being resistant to disintegration upon immersion in or saturation with water, said unit having a porous heterogeneous structure of strongly bonded discrete particles of dried gel of a fineness of at least 100 -mesh and having such strength that a cylindrical test specimen of about 2 mm.
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Description
Reissued Jan. 14,1941
UNITED STATES PATENT OFFICE 21.690 PREPARATION or con'rsc'r MASSES mm AND LIFE GELS THEREOF THE AND PRODUCT George R. Bond, Jr., Baulsboro, N. 1., assignor to Houdry Process Corporation, Dover, not, a corporation of Delaware No Drawing. Original No. 2,148,718, dated Feb Mary 14, 1939, Serial No. 83,309, June 8, 1936. Application for reissue May 23, 1939, Serial No.
24 Claims. :(c1. zse-zwo) the gel, often to the extent of 60 to 75% or more used or proposed for use .as a contact mass in many chemical and physical processes, includ-. ing decolorization and/or clarification or liquids, separation of gases by adsorption, storage of flammable fluids, absorptive processes for refrigeration, the purification of gases and liquids, as well as in catalytic processes,including syntheses and decompositions in both the organic and inorganic chemical fields. Other known gels or gel-like materials having properties which make them suitable for use as contact masses includef-other silicious materials, such for example, assimple silicates of many metals as of aluminum, iron, zinc, copper, vanadium, mag nesium, calcium, tungsten, nickel, manganese, cobalt, cerium; poly-silicates of alumina and other metals, some of which have base exchanging or zeolitic properties; salts containing negative metallic radicals and which can precipitate in gel form, as exemplified by certain alluminates, vanadates, tungstates, stannates and titanates; hydroxides which can be obtained as gels such as the hydroxides of iron, aluminum, chromium, copper, cobalt, nickel, etc.; certain acids such as tungstic, stannic and titanic acids; and mixtures or compounds of the above classes oi substances.
crushed or broken inany desired manner to pro-- duce fragmentary pieces which were screened to rejectthe fines and to select fragments of a size within a desired or acceptable range of sizes. Oversized iragments were further broken and the screening process repeated. a
The drying or hardening operation caused considerable shrinkage or volume reduction oi .oi' the original volume of the mass or filter cake.
The dried cake and subsequently produced fragmentary pieces were dense and extremely'iriable. Because of this friability, large quantities of fines were made during the crushing operation. Furthermore, this property tends to impose practical limits upon the size of fragments. having suflicient mechanical strength to withstand the stresses encountered in ordinary use, and,
in many instances, it was necessary to use beds of extremely small granules or fragments of the contact mass, despite the high resistance which such beds offered to the flow .ot fluids through them. Many of the contact masses prepared from dried gels, in the manner indicated above,
were subject todisintegration when immersed in-certain liquids and even when wetted, whether accidentally or otherwise. This was particularly true of certain silicious gels. Silica gel, for example, disintegrated with almost explosive violence when immersed in water. Other gels were so weakened by wetting that they were rendered unfit for use as contact masses. Consequently, much care and expense were incurred in the packing and shipment of such materials. In' the case of zeolitic water softening agents, itwas necessary to prepare and ship them in a moist or wet state, the water content being usually of the order of 30% by weight, in order. that they might maintain the proper size and shape during shipment and/or use. Heat curing treatment of such materialsv tended to decrease but did not always correct this lack of mechanical stability. I In contact operations it is preferable to present the contact material in pieces of uniform size and shape. This can best be efiected by a molding operation. However, previous attempts to mold wet gel directly have often resulted in complete failure, and when the molding opera tion was at all possible the molded pieces were no better in quality than, and often inferior to, fragmentary pieces produced by the above described method oi! forming a solid cake and then crushing it. Y
The fines made luring the crushing operation, usually amounting to 10 to 15% and sometimes as much as 30% of the original gel, were unavoidable and often represented loss oi! valuable material. Hence, it has been proposed to utilize such fines in the preparation of contact masses despite the tact that, in many instances, masses containing fines'were known to be inferior in quality. One proposal was to rework such fines in a new batch of'the gel. This method of reclaiming fines tended to produce contact masses which were grainy and weak. It was also proposed to prepare molded pieces of the tines by pressing them into briquettes or pellets. Again a physically unstable contact mass was formed. Still another proposal was to mix the fineswith an extraneous binding agent and to mold the mixture. The binder diluted or modified the contact mass, and, in numerous instances, the resulting pieces were decidedly inferior in quality. It has been proposed also to use a binder which could be converted into an active form by treatment of the molded pieces. was proposed as a binding material for silica gel. The molded pieces were to be treated by acid so as to convert the sodium silicate into silica gel. This conversion in many instances was incomplete or required excessive lengths of time and amounts of acid. Furthermore, the treatment was apt to be detrimental to the physical and/or chemical structure of the contact mass. In every case processes designed for reclamation of fines involved a second handling and reprocessing of a substantial proportion of the dried gel. In many instances, expensive equipment and/or additional material including chemical reagents were required.
One object of the present invention is to provide a simple and efilcient method of preparing contact masses from sols, gels or gel-like materials. Another object is to produce from the above materials contact masses in any desired size and shape and in stable form. Another obiect is-to transform such materials into molded pieces of improved porosity and having increased amounts of readily available contact surface. Another object is to produce such masses without the use of extraneous binding materials. Still another objectis to avoid the production of fines or waste material of depreciated value. Still other objects will be apparent from the detailed discussion which follows.
The invention involves a method for producing from a gel a heterogeneous plastic mass which will not shrink to any substantial extent when dried, and which hardens into a coherent body having high mechanical stability. This plastic mass is still, but readily workable, and resembles in many respects'batches of potters and brickmakers molding mixtures. It is peculiarly adapted to forming or molding operations including extrusion, pelletting, etc. According to one aspect of the invention, the essential steps for the preparation of the unshrinkable plastic mass are as follows:
(a) A gel ofthe desired composition is prepared and may then be washed in known manner, with or without removal of excess liquid;
(b) The gel is divided'into two portions;
(c) One portion, usually the predominant proportion of the original gel. is dehydrated to effeet hardening and substantially complete shrinkage thereof and is then reduced to finely divided or comminuted and preferabiy'washed form:
(d) The dried and comminuted portion is then blended with gelatinous material remaining from step (b) to produce a plastic mass of the proper Prior to er during the subsequent forming operation the plastic mass is preferably subjected to substantial pressure in order to eflect compactingof the preshrunk particles and even distribution of'a thin layer of tbewet partof the gel between and around these particles. Us al- For example, sodium silicate greater strength with finer division.
1y, sufi'icient pressure is exerted on the mass when it is forced through an extrusion die or when it is compacted or compressed in the prep- :on drying of the formed pieces, firmly cements dried molded pieces are further characterized by having high physical or mechanical stability, as evidenced by high crus'hing, tensile and shearing strengths and by resistance to disintegration when wet by or immersed in liquids. The most suitable ratio of preshrunk particles to undried material in the plastic mixture varies with the characteristics of the gel and can easily be determined for each gel by simple experi- 3 mer ts. Usually the 'best plastic mixtures are obtained by utilizing dried gel considerably in excess of wet gel, good results being obtained when the ratio of gel which is preshrunk to unmodified gel lies within or above the range of 1:1 to 5.7:1. When a complete batch of gel is utilized this range corresponds to effecting preshrinkage of to 85% of the original material. For silicious materials" good results may be obtained when the ratio iiesa'bove 1.5: 1 as up to 421, or at least to. 80% of the gel-is pre- -r shrunk when a given batch is completely used up.
Moderate temperatures are preferably employed in the preshrinking step. Temperatures which cause sintering of the starting material or removal of excessive amounts of any water of composition from the gel sometimes tend to impair the mechanical stability of the formed pieces. Good results are usually obtained when drying temperatures under 400 F. are used, such, for 5 example, as 180 to 250 F. The strength of the finished piecesof contact mass is to some extent dependent upon the size of the finely divided preshrunk material, the tendency being toward Suitable particle sizes are 60 mesh or liner, and preferably 100 mesh or finer, as up to 400 mesh.
Sometimes it is desired to provide a contact mass containing a plurality of gels. In such cases, the gels may be mixed prior to the preshrinking stepper all or a predetermined proportionof one. or more of the gels may be preshrunk, the re-, maining material serving as the wet portion of.
the plastic mixture. It is sometimes desirable to include non-sei-nke materials in a contact mass, as for example, finely divided metals or metallic compounds. Such material can be mixed with the original gel, but is preferably added to that portion-of the gel which has been the process of being preshrunk.
orisin The step of combining the preshrunk and wet fractions of the gel can be effected inany type of apparatus capable of making a good mixture.
If the mixture is to be extruded and if it is desired to decrease friction by the addition of a lubricant, care should be taken to select a material which will not impair the product and preferably one which will be removed during the subsequent drying operation, such for example as low boiling hydrocarbons or hydrocarbon mixtures, water, etc.
The molded pieces can bedried at any temperature that is consistent with maintenance of the physical and/or chemical stability of the gellike substance or substances comprising the mass. In many instances, drying temperatures within the range specified for the preshrinking step produce pieces having satisfactory strength. Sometimes, however, in order to provide an exceptionally strong bond between the preshrunk and wet portion of the gel it is desirable to use somewhat higher temperatures as up to 600 F. or 700 F. or up to 1000 F. but below the temperature at which the physical or chemical structure of the mass is destroyed as through sintering or elimination of water of combination. When it is desirable to effect tempering or reduction of the catalytic or adsorp'tive properties of the contact mass, drying temperatures which cause change in the structure of the mass can be e plo e The following examples provide specific illustrations of the invention:
Example 1 An aluminum silicate gel was made by the interaction between sodium silicate and ammonium aluminum sulphate. The precipitate was washed and excess water removed as well as possible in a vacuum filter. Approximately 75% of the resulting filter cake was substantially completely dried in a current of air for about hours at about 220 F. and the dried material ground to about 150 mesh. The dried and ground gel was mixed with the remaining portion ofthe wet gel to form a plastic mass which was extruded and cut-to produce cylindrical pieces of about 2 mm. diameter and 4 mm. in length. These were dried at about 220 1'. The dried pieces were strong, porous and highly adsorptive. The individual pieces were capable of resisting concentrated loads as high as 600 grams applied through a knife edge perpendicular to the axis of the cylinder and were capable of absorbingand retaining 95 to 100% of their weight of water. When heated to 600 1".these cylinders resisted concentrated loads of about 900 grams under a knife edge and had about the same absorptive capacity. Even after heating to 600' It, the pieces had substantially the same diameter as wheni'reshly extruded.
Example 2 In order to determine in detail the advantages of the present invention over the former conventional methods of preparing contact masses from gels, a batch of silica gel, which was precipitated and washed in conventional manner, was subjected to different treatments.
First, a fragmented contact mass was prepared in conventional manner.
A portion of the batch was dried at temperatures in the range of 180 to 220 F., duringwhich step the gel shrunk to about 40% of its original volume. The dried material was crushed to produce fragments which were screened to segregate pieces having a size of 4 to 8 mesh. These pieces were then heated to about 700 F. and were examined. The individual fragments were dense and possessed definite cleavage planes. The strengths of these fragments'were not uniform, some of them splitting under conce'ntrated loads as low as 50 grams. When im mersed in water they rapidly disintegrated to small grains, none of which was larger than about 16 mesh. The disintegrated fragments were capable of absorbing about 65% of water by weight.
Second, and in sharp distinction to the above, the remainder of the batch was utilized to 'prepare improved contact masses according to the present invention.
A'plastic mixture was prepared from this remainder by drying and grinding approximately 80% of it, substantially as described in Example 1, and then mixing the dried and ground part with the remaining portion of wet gel.
A portion of this mixture was extruded under a pressure of the order of 1500 pounds per square inch and cut into pellets having a diameter of about 4 mm. and'a length of approximately 4 mm. These pellets were dried at temperatures which were slowly increased to about 600 F. During this operation practically no shrinkage of the pellets occurred. The dried pellets uniformly resisted concentrated loads of about 400 grams. They 'did not disintegrate even when immersed in boiling water and were capable of absorbing more than 100% of water by weight.
The remaining portion of the plastic mixture was not molded but was compressed under a pressure of about 1500-pounds persquare inch and was then dried at temperatures which were slowly increased to about 600 F. in substantially the same manner as the first portion of the plastic mass. Practically no shrinkage of the mass took place during the drying step. The dried mass was broken into fragments, all of which were resistant to disintegration upon immersion in boiling water, even when they were large enough to be retained on a 2 mesh screen. They could absorb about 100% of water by weight. The fragmented pieces were then screened to segregate pieces having a size of 4 to 8 mesh. pieces were uniformly about three times as strong as fragments of the same size prepared in the conventional manner by sodium silicate and nickel ammonium sulphate; The precipitated gel was made into a plastic mixture substantially after the manner describedv in Example 1, approximately 75% of the original gel being dried at. moderate temperature and ground to 150 mesh and flner and then combined with the remaining 25% of the gel. This mixture was then extruded to produce pastilles of about 2 mm. diameter and 4 mm. in length. The pastilles were gradually heated to about 600 F. to effect drying thereof and when dried were substantially the same size as when extruded, were capable of resisting 500 grams concentrated load, and could absorb about 80% by weight of water.
Example 4 A blend of magnesium and aluminum silicates was made by reacting aluminum alum and magnesium sulphate with water-glass. Approximately 75% of the resulting gel was dried and ground substantially as described in Example 1 and mixed, with the remaining portion of the wet gel to produce a plastic mixture. From this mixture molded pellets were produced by extrusion through a die providing 2 mm. openings. The pellets were dried at temperatures within the range 01 400 to 600 F. Again no appreciable shrinkage of the pellets took place. They were capable of resisting concentrated loads of approximately 950 grams and could absorb about 85% water by weight.
Example 5 A zeolitic polysilicate capable of use asa water treating agent was prepared by the reaction between sodium aluminate and sodium silicate. Approximately 75% of the resulting sodium aluminum silicate gel. was preshrunk and ground to 100 mesh and then combined with the re- 1 mainlng wet portion of the gel substantially as described in Example 1. mixture wasmolded into pellets. After drying at temperatures in the range of 180 to 220 F.,:the pellets resisted concentrated loads of about 1000 grams and could absorb approximately 75% water by weight. When immersed in boiling water they did not disintegrate, nor did fragmented pieces prepared by drying and breaking an unextruded portion oi the plastic mixture. Both the extruded and fragmented forms were capable of shipment in a-substantlally bone dry state.
From the very'large number of gels which have been processed according to the present invention venadyl aluminate and stannic acid may be selected as representative of materials at or near the extremities of the range of ratios of the part to be preshrunk and comminuted to. the part retained in wet form. Strong. highly adsorptive molded pieces are produced from vanadyl aluminate when at least 50% of the original gel is dried and ground. In the case of stannic acid a good plastic non-shrinkable mixture is made when approximately 85% or more of the gel is preshrunk.
It is apparent from the above that the present involved in using such substances, and without rerunning or reprocessing substantial proportions of the original gel. The process for making the improved contact masses is extremely simple in character and is efllcient and economical.
When the term knife edge" is used herein and.
in the appended claims it refers-to theedges of knives of the type commonly used to provide bearing suri'aces or iulcrums in analytical and other pressure balances or scales.
I claim as my invention: Y
1. In the process or converting gels into com pact, porous. mechanically stable pieces suitable for use in contact operations, the steps which comprise drying a portion of the gel to eilect substantlally complete shrinkage thereof, then mixing said portion in comminuted iorm with an- The resulting plastic.
other and wet part of said gel, and proportioning said portion and said part so that the resultin mixture is stifi, workable and does not shrink to substantial extent when dried.
2. In treating gels or gel-like material to produce therefrom molded contact masses of .substantially uniform size and shape and of high physical stability, the process steps of drying a portion of the wet gel until substantially complete shrinkage of the same is effected, reducing the resulting shrunken portion to finely divided form, mixing said portion with another and wet portion of said gel, regulating the proportion of shrunken and finely divided gel to wet gel so that the resulting mixture is a plastic mass which does not shrink to substantial extent upon drying,
and molding said mixture under substantial pressure.
3. In the production of contact masses from gels, the steps of preparing from wet gel a plastic mass which is stiff, workable, and which does.
not shrink to substantial extent upon drying comprising eifecting substantially complete shrinkage of a portion only but at least 60% of the wet gel by drying the latter, reducing the shrunken gel to finely divided form, and mixing the fine,
shrunken material with the remaining wet portion of the gel.
4. In the production of physically stable, highly adsorptive contact masses from gels, the process of producing a substantially unshrinkable plastic mixture therefrom comprising providingtwo unequal portions of wet gel or gel-like material, the amount of one of said portions being at least three times the amount of, the other, drying the larger of said portions to effect substantially complete shrinkage of the same and or gel-like material, the amount of one of said portions being at least three times the amount of the other, drying the larger of said portions to eifect substantially complete shrinkage of the same, mixing the two portions, and molding the resulting plastic mixture under substantial pressure.
6. In the preparation of molded contact masses from silicious gels, the process of drying'a portion only but at least 75% of the original gel:at
moderate temperatures until substantially com-- plete shrinkage of that portion is efiected, grinding the shrunken portion to reduce the same to a particle size of a 100 mesh or finer, mixing that portion with the remaining and wet portion of the gel to produce a plastic mixture, molding the latter into pieces of uniform size and shape, and drying the molded pieces at a temperature below that at which substantial change in the structure of the gel takes place.
'7. In the production of highly adsorptive contact masses having high physical stability from silicious gels, the steps of producing a plastic mixture which does not shrink to substantial extent upon drying, comprising drying a portion only but at least 75% of the original and wet gel at a temperature not in excess of 400 F. to effect substantially complete shrinkage oi the same, re-
ducing the dried gel to flnelydivided form, mixingthedriedandflnelydivldedgolwiththanmaining and wet portion thereof, and subjecting the resulting mixture to substantial pressure.
8. In the production of molded contact masses from a prepared gel, the steps of dividing the wet gel into two portions in the ratio of at least 4:1,
drying the larger of said portions until substantially complete shrinkage of the same is efiected,
reducing said dried portion to finely divided form, providing a plastic mass which is substantially unshrinkable upon drying by mixing said dried portion with the smaller and wet portion, and molding said plastic mass into pieces of desired size'and shape under substantial pressure.
finer, providing a plastic mass which does not shrink to substantial extent upon drying by mixing said portion with the smaller and wet portion, molding said plastic mass into pieces of desired size and shape under substantial pressure, and drying said pieces. D
10. In the preparation of highly adsorptive and physically stable pieces of suitable sized and shaped contact masses from gels or gel-like materials, the steps of providing two unequal portions of wet gel, the amount of one of said portions being at least one and one half times the amount of the other, drying the larger of said portions to effect substantially complete shrinkage thereof, reducing the dried portion to finely divided condition, mixing the dried and finely divided portion with the remaining and wet portion to produce a plastic mixture which is substantially' unshrinkable upon drying, adding a.
dry, finely divided material to the gel to adjust the plasticity of the mixture, producing from the latter particles of suitable size. and drying said particles.
11. In the preparation of molded contact masses from gels, the steps of providing two portions of wet silicious gel, the amount of one of said portions being at least three times that of the other, drying the larger of said portions to effect substantially complete shrinkage thereof, reducing the shrunken portion to finely divided condition, adding a suitable amount of dry, finely divided catalytic material to the shrunken portion, mixing the resulting mixture with the remining and wet portion to produce a stiff and workable plastic mixture which does not shrink to substantial extent upon drying, molding said mixture under substantial pressure, and drying the molded mixture. x 12. In the production of physically stable,
highly adsorptive contact masses from gels the, process of producing a plastic mass which does not shrink to substantial extent upon drying and forming said mass into pieces of suitable size and shape comprising the steps of providing two unequal portions of wet gel or gel-like material,
the amount of one of said portions being at least three times the amount of the other, drying the larger of said portions at a temperature in the range of 180 F. to 250 F. until substantially complete shrinkage of said portion is effected, re-
ducing said larger and dried portion to a particle size of 100 mesh or finer, mixing the resulting finely divided material with the remaining and wet portion of gel, washing at least a part of the gel or gel-like material prior to said mixing concentrated load applied step, molding the resulting plastic mixture under a pressure of atleast 800 pounds per square inch 13. An adsorptive preformed unit valuable for use as catalyst or catalyst support consisting of a hard heterogeneous aggregate of finely divided prehardened particles of' synthetic inorganic gel bonded together by a minor quantity of synthetic inorganic gel uniformly distributed among said particles, a cylindrical test piece of the aggregate having a diameter of about 2 mm. being strong enough to support concentrated load of at least 700 grams applied through a knife edge across its axis.
14. An adsorptive molded unit of predetermined size and shape suitable for use as catalyst or catalyst support consisting oi 100 mesh or finer hardened synthetic inorganic gel particles bonded together in a dry, hard, tough, heterogeneous aggregate by a minor quantity of synthetic inorganic gel uniformly distributed throughout the aggregate and between said particles, said unit having adsorptive capacity for water of at least 75% water by weight and being resistant to disintegration upon immersion in or saturation with water, the resistance of said unit to mechanical ganic gel uniformly distributed among and be-- tween said particles'to form a heterogeneous aggregate, a cylindrical test piece of which having a diameter of about 2 mm. will support a concentrated load of at least 900 grams applied through a knife edge across its axis.
16. A highly adsorptive molded unit valuable for use as catalyst or catalyst support consisting of plural oxide synthetic inorganic gel, said unit being composed of prehardened particles of synthetic gel of 60 mesh size or smaller bonded together in a porous, tough, hard heterogeneous aggregate by a further quantity of the same gel uniformly distributed among said particles by mixture therewith and limited to such minor amount that test pieces of the aggregate in the form of cylinders of about 2 mm. diameter will support at least 900 grams concentrated loadapplied through a knife edge across its axis. 1.
17. A rigid heterogeneous preformed aggregate adapted for use as catalyst or catalyst support I thetic inorganic gel uniformly distributed between and around said particles and cementing the latter together in a hard, tough, porous body. a cylindrical test piece of which having a diameter of about 2 mm. will support a least 900 grams ugh a knife edge across its axis. 18. An adsorptive unit valuable for use as catalyst or catalyst support comprising a preformed body of 2 to 4 mm. diameter consisting of finely divided particles of synthetic inorganic gel bonded together in aheterogeneous dry, hard aggregate by a further but minor quantity of synthetic inorganic gel which had been mixed in the wet state with said .particles,said body .having such high resistance to mechanical stress that a cylindrical test piece of the dry, hard aggregate having a diameter of about 2 mm. will support at least I00 grams concentrated load applied through a knife edge across its axis.
19. A molded, rigid heterogeneous aggregate suitable for use as catalyst or catalyst support consisting oi'iinely divided particles of a plural oxide silicious gel bonded together by a further quantity of silicious gel, which had been uniformly distributed in wet state between and around said particles and subsequently hardened, the gel in wet state being limited to such minor amount that the hardened aggregate is resistant to disintegration upon immersion in or saturation with water and has such resistance to mechanical stress that a cylindrical specimen of the aggregate having a diameter'of about 2 mm. will support at least 900 grams concentrated load applied through a knife edge across its axis.
20. A tough, rigid molded contact unit valuable for use as catalyst or catalyst support consisting of synthetic inorganic gel, said unit being a heterogeneous aggregate of prehardened finely divided particles of said gel of 100 mesh or finer bonded together by a further but minor quantity of said gel which had been uniformly mixed in wet state with said prehardened particles and the resulting aggregate subsequently hardened,
a cylindrical specimen of the aggregate having a lubricating and binding material containing v synthetic inorganic gelatinous substance as the sole binding agent, proportioning said gel and said material so that the resulting heterogeneous mixture contains only a minor quantity of said substance and is stii! and workable but willnot shrink to substantial 'extent upon drying, moldingsaid mixture into' pieces of predetermined size and shape, and heating the molded pieces to dry them and to yield a product, cylindrical test pieces of which of about 2 mm. diameter will support concentrated loads of' at least 700 grams applied through a knife edge perpendicular to their axes.
22. The process of making-molded contact masses valuable for use as catalyst or catalyst supportv consisting of inorganic synthetic gel comprising the steps of reducing hardened and preshrunk synthetic silicious gel to particles of 100 mesh size or finer, mixing said particles and geneous mixture contains only a minor quantity of said substance and is stiff and workable but will not shrink to substantial extent upon drying, molding said mixture under pressure into pieces of predetermined size and shape, and heating said pieces to dry and harden the same into rigid form having high mechanical strength, a test piece of which in the form of a cylinder having a diameter of about 2 mm. will support concentrated loads of at least 500 grams applied through a knife edge across the axis of said cylinder.
23. A contact mass valuable for use as catalyst or catalyst support consisting wholly of the-same precipitated inorganic gel and comprising a dry, hard molded unit having high adsorptive ca-' pacity for water and being resistant to disinte gration upon immersion in or saturation with water, said unit having a porous heterogeneous structure of strongly bonded discrete particles of dried gel of a fineness of at least 100 mesh and having such strength that a cylindrical test specimen of about 2 mm. diameter will support at least 700 grams concentrated load applied across its axis, said unit being identical with the product produced by reducing said gel to prehardened and preshrunk finely divided condition, incorporating with the finely divided gel a lubricating and binding material containing synthetic inorganic gelatinous substance as the sole binding agent, proportioning said gel and said material so that the resulting heterogeneous mix- I ture contains only a minor quantity of said substance and is still and workable but will not shrink to substantial extent upon drying, molding the mixture into pieces of predetermined size and shape, and heating the molded pieces to dry and harden them.
24. A contact mass valuable for use as a catalyst or catalyst support consisting wholly oi the same precipitated silica-alumina gel and comprising a dry, hard molded unit having high adsorptive capacity for water and being resistant to disintegration upon immersion in or saturation with water, said unit having a porous heterogeneous structure of strongly bonded discrete particles of dried gel of a fineness of at least 100 -mesh and having such strength that a cylindrical test specimen of about 2 mm. diameter will support at least 700 grams concentrated, load applied across its axis, said unit being identical with the product produced by reducing said gel to prehardened and preshrunk finely divided condition, incorporating with the finely divided gel a lubricating and binding material containing synthetic inorganic gelatinous substance as the sole binding agent, proportioning said gel and said material so that v the resulting heterogeneous mixture contains only a minor quantity of said substance and is stiff and workable but will not shrink to substantial extent upon drying, molding the mixture into pieces of predetermined size and shape, and heating the molded pieces to dry and harden them. GEORGE R. BOND, JR.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US83309A US2146718A (en) | 1936-06-03 | 1936-06-03 | Preparation of contact masses from gels and the like |
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|---|---|
| USRE21690E true USRE21690E (en) | 1941-01-14 |
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| US83309A Expired - Lifetime US2146718A (en) | 1936-06-03 | 1936-06-03 | Preparation of contact masses from gels and the like |
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| Application Number | Title | Priority Date | Filing Date |
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| US83309A Expired - Lifetime US2146718A (en) | 1936-06-03 | 1936-06-03 | Preparation of contact masses from gels and the like |
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Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2419272A (en) * | 1944-04-26 | 1947-04-22 | Socony Vacuum Oil Co Inc | Process of forming a silicacontaining hydrogel |
| US2428798A (en) * | 1945-06-12 | 1947-10-14 | Socony Vacuum Oil Co Inc | Hydrocarbon conversion in presence of gel catalysts |
| US2459987A (en) * | 1946-05-07 | 1949-01-25 | Standard Oil Dev Co | Mixed silica-alumina, silica-magnesia catalyst |
| US2487600A (en) * | 1945-10-09 | 1949-11-08 | Sharp & Dohme Inc | Aqueous thixotropic gel composition |
| US2487065A (en) * | 1944-04-05 | 1949-11-08 | Houdry Process Corp | Preparation of gel catalysts |
| US2511740A (en) * | 1949-10-05 | 1950-06-13 | Sharp & Dohme Inc | Stabilized thixotrpic gels |
| US2529461A (en) * | 1949-04-30 | 1950-11-07 | Sharp & Dohme Inc | Emulsions |
| US2529460A (en) * | 1949-04-30 | 1950-11-07 | Sharp & Dohme Inc | Emulsions containing resins |
| US2562888A (en) * | 1947-12-26 | 1951-08-07 | Houdry Process Corp | Preparation of a silica-metal oxide granular catalyst |
| US5434118A (en) * | 1990-12-21 | 1995-07-18 | Eniricerche S.P.A. | Catalytically active gel and a process for its preparation |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2429981A (en) * | 1939-12-23 | 1947-11-04 | Houdry Process Corp | Conversion of hydrocarbons with alkali metal-free catalyst comprising silica and amphoteric oxide |
| US2415441A (en) * | 1941-01-02 | 1947-02-11 | Houdry Process Corp | Preparation of contact materials |
| US2433869A (en) * | 1944-03-09 | 1948-01-06 | Houdry Process Corp | Preparation of contact masses |
| US2481824A (en) * | 1944-10-04 | 1949-09-13 | California Research Corp | Dehydrogenation of hydrocarbon oil and catalyst therefor |
| US2438450A (en) * | 1945-02-17 | 1948-03-23 | Standard Oil Dev Co | Drying of microspherical gelas |
| US2481841A (en) * | 1945-11-02 | 1949-09-13 | Standard Oil Dev Co | Method of preparing catalyst particles having nuclei of previously calcined fines |
| US2618615A (en) * | 1949-01-24 | 1952-11-18 | Standard Oil Dev Co | Forming silica-containing gel particles into strong tablets |
| US2535948A (en) * | 1949-03-25 | 1950-12-26 | Davison Chemical Corp | Incorporation of fines in a silicaalumina catalyst |
| US2650202A (en) * | 1951-02-15 | 1953-08-25 | Tide Water Associated Oil Comp | Production of silicate adsorbent |
| US2650203A (en) * | 1951-02-15 | 1953-08-25 | Tide Water Associated Oil Comp | Preparation of silicate adsorbents |
| US4617108A (en) * | 1985-05-20 | 1986-10-14 | Phillips Petroleum Company | Process for cracking with silica-alumina |
-
0
- US US21690D patent/USRE21690E/en not_active Expired
-
1936
- 1936-06-03 US US83309A patent/US2146718A/en not_active Expired - Lifetime
Cited By (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2487065A (en) * | 1944-04-05 | 1949-11-08 | Houdry Process Corp | Preparation of gel catalysts |
| US2419272A (en) * | 1944-04-26 | 1947-04-22 | Socony Vacuum Oil Co Inc | Process of forming a silicacontaining hydrogel |
| US2428798A (en) * | 1945-06-12 | 1947-10-14 | Socony Vacuum Oil Co Inc | Hydrocarbon conversion in presence of gel catalysts |
| US2487600A (en) * | 1945-10-09 | 1949-11-08 | Sharp & Dohme Inc | Aqueous thixotropic gel composition |
| US2459987A (en) * | 1946-05-07 | 1949-01-25 | Standard Oil Dev Co | Mixed silica-alumina, silica-magnesia catalyst |
| US2562888A (en) * | 1947-12-26 | 1951-08-07 | Houdry Process Corp | Preparation of a silica-metal oxide granular catalyst |
| US2529461A (en) * | 1949-04-30 | 1950-11-07 | Sharp & Dohme Inc | Emulsions |
| US2529460A (en) * | 1949-04-30 | 1950-11-07 | Sharp & Dohme Inc | Emulsions containing resins |
| US2511740A (en) * | 1949-10-05 | 1950-06-13 | Sharp & Dohme Inc | Stabilized thixotrpic gels |
| US5434118A (en) * | 1990-12-21 | 1995-07-18 | Eniricerche S.P.A. | Catalytically active gel and a process for its preparation |
| US5578744A (en) * | 1990-12-21 | 1996-11-26 | Eniricerche S.P.A. | Catalytically active gel and a process for its preparation |
Also Published As
| Publication number | Publication date |
|---|---|
| US2146718A (en) | 1939-02-14 |
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