SK280237B6 - Spôsob prípravy polymérov karboxylátu oxidu hlinit - Google Patents
Spôsob prípravy polymérov karboxylátu oxidu hlinit Download PDFInfo
- Publication number
- SK280237B6 SK280237B6 SK2179-90A SK217990A SK280237B6 SK 280237 B6 SK280237 B6 SK 280237B6 SK 217990 A SK217990 A SK 217990A SK 280237 B6 SK280237 B6 SK 280237B6
- Authority
- SK
- Slovakia
- Prior art keywords
- alkanol
- aluminum
- water
- reaction
- solution
- Prior art date
Links
- -1 aluminium oxide carboxylate Chemical class 0.000 title claims abstract description 33
- 229920000642 polymer Polymers 0.000 title claims abstract description 21
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 title claims description 24
- 238000004519 manufacturing process Methods 0.000 title description 5
- 229910052782 aluminium Inorganic materials 0.000 claims abstract description 48
- 238000000034 method Methods 0.000 claims abstract description 48
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 39
- 238000006243 chemical reaction Methods 0.000 claims abstract description 33
- 150000002148 esters Chemical class 0.000 claims abstract description 23
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims abstract description 20
- 239000000203 mixture Substances 0.000 claims abstract description 19
- 238000009835 boiling Methods 0.000 claims abstract description 12
- 238000002360 preparation method Methods 0.000 claims abstract description 11
- 150000002763 monocarboxylic acids Chemical class 0.000 claims abstract description 10
- 239000002904 solvent Substances 0.000 claims abstract description 9
- 150000001735 carboxylic acids Chemical class 0.000 claims abstract description 6
- 125000001931 aliphatic group Chemical group 0.000 claims abstract description 3
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 claims abstract description 3
- 239000011541 reaction mixture Substances 0.000 claims abstract description 3
- 150000007942 carboxylates Chemical class 0.000 claims description 14
- 239000012071 phase Substances 0.000 claims description 8
- 125000003545 alkoxy group Chemical group 0.000 claims description 5
- 125000004432 carbon atom Chemical group C* 0.000 claims description 5
- 239000006260 foam Substances 0.000 claims description 4
- 239000007791 liquid phase Substances 0.000 claims description 4
- SMZOGRDCAXLAAR-UHFFFAOYSA-N aluminium isopropoxide Chemical group [Al+3].CC(C)[O-].CC(C)[O-].CC(C)[O-] SMZOGRDCAXLAAR-UHFFFAOYSA-N 0.000 claims description 3
- 229930195733 hydrocarbon Natural products 0.000 claims description 3
- 150000002430 hydrocarbons Chemical class 0.000 claims description 3
- 239000004215 Carbon black (E152) Substances 0.000 claims description 2
- 125000003118 aryl group Chemical group 0.000 claims 1
- 230000000977 initiatory effect Effects 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 abstract description 5
- 150000004945 aromatic hydrocarbons Chemical class 0.000 abstract description 2
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 24
- 239000000047 product Substances 0.000 description 22
- 239000000243 solution Substances 0.000 description 21
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 12
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 9
- 230000015572 biosynthetic process Effects 0.000 description 9
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 6
- 238000001556 precipitation Methods 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 4
- 125000004122 cyclic group Chemical group 0.000 description 4
- 239000007790 solid phase Substances 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 235000021355 Stearic acid Nutrition 0.000 description 3
- 150000004703 alkoxides Chemical class 0.000 description 3
- 239000006227 byproduct Substances 0.000 description 3
- 238000001914 filtration Methods 0.000 description 3
- 239000000295 fuel oil Substances 0.000 description 3
- 229940089456 isopropyl stearate Drugs 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 3
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 3
- MVLVMROFTAUDAG-UHFFFAOYSA-N octadecanoic acid ethyl ester Natural products CCCCCCCCCCCCCCCCCC(=O)OCC MVLVMROFTAUDAG-UHFFFAOYSA-N 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- ZPWFUIUNWDIYCJ-UHFFFAOYSA-N propan-2-yl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC(C)C ZPWFUIUNWDIYCJ-UHFFFAOYSA-N 0.000 description 3
- 239000008117 stearic acid Substances 0.000 description 3
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 description 2
- JPUHCPXFQIXLMW-UHFFFAOYSA-N aluminium triethoxide Chemical compound CCO[Al](OCC)OCC JPUHCPXFQIXLMW-UHFFFAOYSA-N 0.000 description 2
- 239000003849 aromatic solvent Substances 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 230000007062 hydrolysis Effects 0.000 description 2
- 238000006460 hydrolysis reaction Methods 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000013638 trimer Substances 0.000 description 2
- HNNQYHFROJDYHQ-UHFFFAOYSA-N 3-(4-ethylcyclohexyl)propanoic acid 3-(3-ethylcyclopentyl)propanoic acid Chemical compound CCC1CCC(CCC(O)=O)C1.CCC1CCC(CCC(O)=O)CC1 HNNQYHFROJDYHQ-UHFFFAOYSA-N 0.000 description 1
- 229910018516 Al—O Inorganic materials 0.000 description 1
- 229910018514 Al—O—N Inorganic materials 0.000 description 1
- OHILZCHMZDZSLZ-UHFFFAOYSA-N CC(O)[AlH2] Chemical compound CC(O)[AlH2] OHILZCHMZDZSLZ-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- BZDRWQZUTRBGCP-UHFFFAOYSA-N alumanylformic acid Chemical compound OC([AlH2])=O BZDRWQZUTRBGCP-UHFFFAOYSA-N 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 239000012159 carrier gas Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- 230000001143 conditioned effect Effects 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 239000012847 fine chemical Substances 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 239000003349 gelling agent Substances 0.000 description 1
- 125000005456 glyceride group Chemical group 0.000 description 1
- 230000001939 inductive effect Effects 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 239000010985 leather Substances 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 150000007524 organic acids Chemical group 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 239000012265 solid product Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 239000012808 vapor phase Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M119/00—Lubricating compositions characterised by the thickener being a macromolecular compound
- C10M119/30—Lubricating compositions characterised by the thickener being a macromolecular compound containing atoms of elements not provided for in groups C10M119/02 - C10M119/28
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G79/00—Macromolecular compounds obtained by reactions forming a linkage containing atoms other than silicon, sulfur, nitrogen, oxygen, and carbon with or without the latter elements in the main chain of the macromolecule
- C08G79/10—Macromolecular compounds obtained by reactions forming a linkage containing atoms other than silicon, sulfur, nitrogen, oxygen, and carbon with or without the latter elements in the main chain of the macromolecule a linkage containing aluminium
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K3/00—Materials not provided for elsewhere
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2227/00—Organic non-macromolecular compounds containing atoms of elements not provided for in groups C10M2203/00, C10M2207/00, C10M2211/00, C10M2215/00, C10M2219/00 or C10M2223/00 as ingredients in lubricant compositions
- C10M2227/09—Complexes with metals
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Health & Medical Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Polymers & Plastics (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Compounds Of Alkaline-Earth Elements, Aluminum Or Rare-Earth Metals (AREA)
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
HU892076A HU201343B (en) | 1989-05-03 | 1989-05-03 | Process for producing aluminium-oxide-carboxylate polymeres containing not more than 2 mass % of esters |
Publications (2)
Publication Number | Publication Date |
---|---|
SK217990A3 SK217990A3 (en) | 1999-10-08 |
SK280237B6 true SK280237B6 (sk) | 1999-10-08 |
Family
ID=10957647
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SK2179-90A SK280237B6 (sk) | 1989-05-03 | 1990-05-02 | Spôsob prípravy polymérov karboxylátu oxidu hlinit |
Country Status (7)
Country | Link |
---|---|
US (1) | US5075473A (it) |
CH (1) | CH679777A5 (it) |
CZ (1) | CZ282849B6 (it) |
DE (1) | DE4011783C2 (it) |
HU (1) | HU201343B (it) |
IT (1) | IT1240634B (it) |
SK (1) | SK280237B6 (it) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE10011333A1 (de) * | 2000-03-10 | 2001-09-20 | Rwe Dea Ag | Verdickungsmittel-Komponente und Aluminiumkomplex-Schmierfett |
CN104211968B (zh) * | 2014-09-17 | 2017-01-25 | 浙江省中明化工科技有限公司 | 一种以二羟基羧酸铝中间体制备矿物油基铝‑氧聚合物的制备工艺 |
Family Cites Families (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2744074A (en) * | 1951-04-18 | 1956-05-01 | Du Pont | Polymeric organic aluminum oxides and method for preparing same |
DE1032543B (de) * | 1953-04-04 | 1958-06-19 | Hoechst Ag | Verfahren zur Herstellung von organischen aluminiumhaltigen Kunststoffen |
GB806113A (en) * | 1955-02-11 | 1958-12-17 | Hardman & Holden Ltd | Improvements relating to aluminium alcoholate derivatives |
US2925430A (en) * | 1955-02-18 | 1960-02-16 | Konink Ind Mij Voorheen Noury | Polymeric basic aluminum compounds of organic acids |
US2979497A (en) * | 1957-02-12 | 1961-04-11 | J W Ayers & Co | Cyclic aluminum oxide acylates, alkoxides, and phenoxides |
GB825878A (en) * | 1957-07-25 | 1959-12-23 | Hardman & Holden Ltd | Improvements relating to polymeric reaction products of aluminium alkoxides |
DE1130178B (de) * | 1958-04-03 | 1962-05-24 | Hardman & Holden Ltd | Verfahren zur Herstellung von polymeren Alkoxyaluminium-verbindungen |
US3054816A (en) * | 1958-06-30 | 1962-09-18 | Agrashell Inc | Cyclic alkoxy- and phenoxy-aluminum oxide trimers and process for making same |
FR1555831A (it) * | 1967-12-18 | 1969-01-31 | ||
BE789551A (fr) * | 1971-10-01 | 1973-03-29 | Unilever Emery | Nouveaux composes organometalliques |
-
1989
- 1989-05-03 HU HU892076A patent/HU201343B/hu unknown
-
1990
- 1990-04-11 DE DE4011783A patent/DE4011783C2/de not_active Expired - Fee Related
- 1990-05-02 SK SK2179-90A patent/SK280237B6/sk not_active IP Right Cessation
- 1990-05-02 CH CH1487/90A patent/CH679777A5/de not_active IP Right Cessation
- 1990-05-02 CZ CS902179A patent/CZ282849B6/cs not_active IP Right Cessation
- 1990-05-03 IT IT20204A patent/IT1240634B/it active IP Right Grant
- 1990-05-03 US US07/521,048 patent/US5075473A/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
SK217990A3 (en) | 1999-10-08 |
HU201343B (en) | 1990-10-28 |
DE4011783A1 (de) | 1990-11-08 |
IT9020204A0 (it) | 1990-05-03 |
CH679777A5 (it) | 1992-04-15 |
US5075473A (en) | 1991-12-24 |
DE4011783C2 (de) | 1997-07-10 |
CZ282849B6 (cs) | 1997-11-12 |
CZ217990A3 (en) | 1997-07-16 |
IT1240634B (it) | 1993-12-17 |
IT9020204A1 (it) | 1991-11-03 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
MM4A | Patent lapsed due to non-payment of maintenance fees |
Effective date: 20090502 |