GB701349A - Improvements in or relating to the manufacture of alumina sols and catalysts therefrom - Google Patents
Improvements in or relating to the manufacture of alumina sols and catalysts therefromInfo
- Publication number
- GB701349A GB701349A GB2618/52A GB261852A GB701349A GB 701349 A GB701349 A GB 701349A GB 2618/52 A GB2618/52 A GB 2618/52A GB 261852 A GB261852 A GB 261852A GB 701349 A GB701349 A GB 701349A
- Authority
- GB
- United Kingdom
- Prior art keywords
- aluminium
- alumina
- alcohol
- acid
- alcoholate
- 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
Links
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 title abstract 8
- 239000003054 catalyst Substances 0.000 title abstract 5
- 238000004519 manufacturing process Methods 0.000 title 1
- 239000004411 aluminium Substances 0.000 abstract 7
- 229910052782 aluminium Inorganic materials 0.000 abstract 7
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 abstract 6
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 abstract 5
- 235000019441 ethanol Nutrition 0.000 abstract 5
- 239000004215 Carbon black (E152) Substances 0.000 abstract 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 4
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 abstract 4
- 239000003795 chemical substances by application Substances 0.000 abstract 4
- 229930195733 hydrocarbon Natural products 0.000 abstract 4
- 150000002430 hydrocarbons Chemical class 0.000 abstract 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 abstract 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 abstract 3
- 238000006243 chemical reaction Methods 0.000 abstract 3
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 abstract 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 3
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 abstract 2
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 abstract 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 abstract 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract 2
- PQLAYKMGZDUDLQ-UHFFFAOYSA-K aluminium bromide Chemical compound Br[Al](Br)Br PQLAYKMGZDUDLQ-UHFFFAOYSA-K 0.000 abstract 2
- -1 aluminium halide Chemical class 0.000 abstract 2
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 abstract 2
- 238000009835 boiling Methods 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- 239000007863 gel particle Substances 0.000 abstract 2
- 230000007062 hydrolysis Effects 0.000 abstract 2
- 238000006460 hydrolysis reaction Methods 0.000 abstract 2
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 abstract 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 abstract 2
- 239000000463 material Substances 0.000 abstract 2
- 229960002523 mercuric chloride Drugs 0.000 abstract 2
- LWJROJCJINYWOX-UHFFFAOYSA-L mercury dichloride Chemical compound Cl[Hg]Cl LWJROJCJINYWOX-UHFFFAOYSA-L 0.000 abstract 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 abstract 2
- 238000000034 method Methods 0.000 abstract 2
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 abstract 2
- 239000003208 petroleum Substances 0.000 abstract 2
- 239000011347 resin Substances 0.000 abstract 2
- 229920005989 resin Polymers 0.000 abstract 2
- 239000008096 xylene Substances 0.000 abstract 2
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 abstract 1
- AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 abstract 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract 1
- AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 abstract 1
- 239000004115 Sodium Silicate Substances 0.000 abstract 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 1
- 238000005341 cation exchange Methods 0.000 abstract 1
- 238000001816 cooling Methods 0.000 abstract 1
- 239000003995 emulsifying agent Substances 0.000 abstract 1
- 125000005909 ethyl alcohol group Chemical group 0.000 abstract 1
- 235000019253 formic acid Nutrition 0.000 abstract 1
- 239000007789 gas Substances 0.000 abstract 1
- 239000008131 herbal destillate Substances 0.000 abstract 1
- 229910000042 hydrogen bromide Inorganic materials 0.000 abstract 1
- 229910000041 hydrogen chloride Inorganic materials 0.000 abstract 1
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 abstract 1
- 238000005342 ion exchange Methods 0.000 abstract 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 abstract 1
- 239000004310 lactic acid Substances 0.000 abstract 1
- 235000014655 lactic acid Nutrition 0.000 abstract 1
- 239000007788 liquid Substances 0.000 abstract 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 abstract 1
- 230000008929 regeneration Effects 0.000 abstract 1
- 238000011069 regeneration method Methods 0.000 abstract 1
- 238000000926 separation method Methods 0.000 abstract 1
- 239000000377 silicon dioxide Substances 0.000 abstract 1
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 abstract 1
- 229910052911 sodium silicate Inorganic materials 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
- 238000005406 washing Methods 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01F—COMPOUNDS OF THE METALS BERYLLIUM, MAGNESIUM, ALUMINIUM, CALCIUM, STRONTIUM, BARIUM, RADIUM, THORIUM, OR OF THE RARE-EARTH METALS
- C01F7/00—Compounds of aluminium
- C01F7/02—Aluminium oxide; Aluminium hydroxide; Aluminates
- C01F7/34—Preparation of aluminium hydroxide by precipitation from solutions containing aluminium salts
- C01F7/36—Preparation of aluminium hydroxide by precipitation from solutions containing aluminium salts from organic aluminium salts
-
- 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
- B01J21/00—Catalysts comprising the elements, oxides, or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium, or hafnium
- B01J21/02—Boron or aluminium; Oxides or hydroxides thereof
- B01J21/04—Alumina
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Geology (AREA)
- Inorganic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Catalysts (AREA)
Abstract
Solutions of aluminium alcoholates, hydrolysable in the presence of a peptizing agent to form alumina hydrosols (see Group III), are prepared by dissolving aluminium in an aliphatic alcohol containing from 2-10 carbon atoms in the presence of a catalyst. Amyl, tertiary butyl, isopropyl, and ethyl alcohols are referred to. Suitable catalysts are mercuric chloride, iodine, and aluminium halide. A hydrocarbon, e.g. heptane, octane, toluene, benzene, xylene, or a petroleum fraction boiling from 180-500 DEG F., may be added to the alcohol to control the temperature of the reaction and to serve as a solvent for the alcoholate. Reaction may be carried out under atmospheric or super-atmospheric pressure at a temperature of 200 DEG -300 DEG F. Heat is supplied initially and then the heat of reaction removed by cooling.ALSO:Alumina hydrosol is prepared by hydrolysis of an anhydrous solution of an aluminium alcoholate in the presence of a peptizing agent which is added to the alcoholate solution before the addition of water. Specified peptizing agents are acetic acid, aluminium chloride, aluminium bromide, hydrogen chloride, hydrogen bromide, formic acid, lactic acid, glycollic acid. Preferred amounts of peptizing agent are 1/10 -2 parts by weight per part of alumina. To form the alcoholate, aluminium may be dissolved under pressure at about 200 DEG -300 DEG F. in an aliphatic alcohol of 2-10 carbon atoms, preferably water-insoluble, in the presence of a catalyst, e.g. mercuric chloride, iodine, or aluminium halide; in examples isopropyl alcohol and amyl alcohol are used to dissolve the aluminium. From 0-90 per cent. of a hydrocarbon, e.g. heptane, octane, toluene, benzene, xylene, or a petroleum fraction boiling from 180 DEG -500 DEG F. may be mixed with the alcohol in order to facilitate subsequent separation. Hydrolysis is effected by mixing with water at 65 DEG -220 DEG F., and the product may be aged for at least 15 minutes at 70 DEG -210 DEG F. and separated into two layers; the upper layer of regenerated alcohol and hydrocarbon is heated to remove water, and then used again in the process; the lower alumina sol is heated to remove alcohol and hydrocarbon, and aged for 1-20 hours at a pH of 3-7. To prepare silica-alumina catalysts the alumina sol, which may contain 1-8 per cent. alumina, is mixed with a silica sol containing 3-15 per cent. silica. The silica sol is obtained by contacting sodium silicate solution with an acid-regenerated cation exchange material by a four-stage process involving washing and regeneration of the ion exchange material; preferably a bed of weak acid-type resin is superimposed on a bed of strong acid-type resin; the silica sol may be aged for 1-20 hours at 80 DEG -180 DEG F., and preferably has a pH of 2-7. The mixed sols may be dried and ground, or they may be sprayed into hot gas to obtain microspherical gel particles; alternatively they may be sprayed above or into a body of heated organic liquid which may contain an emulsifying agent. The gel particles may be further dried and activated at 800-1400 DEG F.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US701349XA | 1951-03-06 | 1951-03-06 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB701349A true GB701349A (en) | 1953-12-23 |
Family
ID=22093349
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB2618/52A Expired GB701349A (en) | 1951-03-06 | 1952-01-31 | Improvements in or relating to the manufacture of alumina sols and catalysts therefrom |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB701349A (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1020609B (en) * | 1954-12-01 | 1957-12-12 | Exxon Research Engineering Co | Process for the production of platinum metal catalysts on alumina carriers |
| DE1052365B (en) * | 1955-08-18 | 1959-03-12 | Exxon Research Engineering Co | Process for the production of an abrasion-resistant alumina catalyst carrier |
| DE1161240B (en) * | 1955-07-14 | 1964-01-16 | Engelhard Ind Inc | Process for the production of aluminum oxide carrier catalysts |
| EP0063034A3 (en) * | 1981-04-10 | 1983-04-20 | Zirconal Processes Limited | Rigid coherent gel |
-
1952
- 1952-01-31 GB GB2618/52A patent/GB701349A/en not_active Expired
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1020609B (en) * | 1954-12-01 | 1957-12-12 | Exxon Research Engineering Co | Process for the production of platinum metal catalysts on alumina carriers |
| DE1161240B (en) * | 1955-07-14 | 1964-01-16 | Engelhard Ind Inc | Process for the production of aluminum oxide carrier catalysts |
| DE1052365B (en) * | 1955-08-18 | 1959-03-12 | Exxon Research Engineering Co | Process for the production of an abrasion-resistant alumina catalyst carrier |
| EP0063034A3 (en) * | 1981-04-10 | 1983-04-20 | Zirconal Processes Limited | Rigid coherent gel |
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