GB829634A - Esters of polymeric hydroxyl compounds and boric acid - Google Patents
Esters of polymeric hydroxyl compounds and boric acidInfo
- Publication number
- GB829634A GB829634A GB366057A GB366057A GB829634A GB 829634 A GB829634 A GB 829634A GB 366057 A GB366057 A GB 366057A GB 366057 A GB366057 A GB 366057A GB 829634 A GB829634 A GB 829634A
- Authority
- GB
- United Kingdom
- Prior art keywords
- boric acid
- esters
- hydroxyl compounds
- hydroxyl group
- polymeric hydroxyl
- 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
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 title abstract 5
- 239000004327 boric acid Substances 0.000 title abstract 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 title abstract 4
- 150000002148 esters Chemical class 0.000 title 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 3
- GQEZCXVZFLOKMC-UHFFFAOYSA-N 1-hexadecene Chemical compound CCCCCCCCCCCCCCC=C GQEZCXVZFLOKMC-UHFFFAOYSA-N 0.000 abstract 2
- HFDVRLIODXPAHB-UHFFFAOYSA-N 1-tetradecene Chemical compound CCCCCCCCCCCCC=C HFDVRLIODXPAHB-UHFFFAOYSA-N 0.000 abstract 2
- 150000001336 alkenes Chemical class 0.000 abstract 2
- 125000005907 alkyl ester group Chemical group 0.000 abstract 2
- 239000000203 mixture Substances 0.000 abstract 2
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 abstract 1
- FERIUCNNQQJTOY-UHFFFAOYSA-M Butyrate Chemical compound CCCC([O-])=O FERIUCNNQQJTOY-UHFFFAOYSA-M 0.000 abstract 1
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Natural products CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 abstract 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 abstract 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 abstract 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 abstract 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 abstract 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 abstract 1
- 150000001639 boron compounds Chemical class 0.000 abstract 1
- 229910052810 boron oxide Inorganic materials 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 238000005336 cracking Methods 0.000 abstract 1
- JKWMSGQKBLHBQQ-UHFFFAOYSA-N diboron trioxide Chemical compound O=BOB=O JKWMSGQKBLHBQQ-UHFFFAOYSA-N 0.000 abstract 1
- 239000000446 fuel Substances 0.000 abstract 1
- 230000036571 hydration Effects 0.000 abstract 1
- 238000006703 hydration reaction Methods 0.000 abstract 1
- 238000005984 hydrogenation reaction Methods 0.000 abstract 1
- 230000007062 hydrolysis Effects 0.000 abstract 1
- 238000006460 hydrolysis reaction Methods 0.000 abstract 1
- 239000010687 lubricating oil Substances 0.000 abstract 1
- 239000000178 monomer Substances 0.000 abstract 1
- CCCMONHAUSKTEQ-UHFFFAOYSA-N octadecene Natural products CCCCCCCCCCCCCCCCC=C CCCMONHAUSKTEQ-UHFFFAOYSA-N 0.000 abstract 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 abstract 1
- 230000003647 oxidation Effects 0.000 abstract 1
- 238000007254 oxidation reaction Methods 0.000 abstract 1
- 239000012188 paraffin wax Substances 0.000 abstract 1
- 229920000642 polymer Polymers 0.000 abstract 1
- 238000006116 polymerization reaction Methods 0.000 abstract 1
- TVDSBUOJIPERQY-UHFFFAOYSA-N prop-2-yn-1-ol Chemical compound OCC#C TVDSBUOJIPERQY-UHFFFAOYSA-N 0.000 abstract 1
- 229940095068 tetradecene Drugs 0.000 abstract 1
- LGQXXHMEBUOXRP-UHFFFAOYSA-N tributyl borate Chemical class CCCCOB(OCCCC)OCCCC LGQXXHMEBUOXRP-UHFFFAOYSA-N 0.000 abstract 1
- 239000008096 xylene Substances 0.000 abstract 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
- C10M1/00—Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants
- C10M1/08—Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants with additives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F5/00—Compounds containing elements of Groups 3 or 13 of the Periodic Table
- C07F5/02—Boron compounds
- C07F5/04—Esters of boric acids
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F8/00—Chemical modification by after-treatment
- C08F8/42—Introducing metal atoms or metal-containing groups
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/30—Organic compounds compounds not mentioned before (complexes)
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/30—Organic compounds compounds not mentioned before (complexes)
- C10L1/301—Organic compounds compounds not mentioned before (complexes) derived from metals
- C10L1/303—Organic compounds compounds not mentioned before (complexes) derived from metals boron compounds
-
- 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
- C10M2227/06—Organic compounds derived from inorganic acids or metal salts
- C10M2227/061—Esters derived from boron
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Abstract
Boric acid esters of polymeric hydroxyl compounds are prepared by reacting, e.g. in xylene or benzene, a boron compound (such as boric acid, boron oxide or an alkyl ester of boric acid) with a polymer obtained by copolymerizing an olefin of at least 8 carbon atoms with a polymerizable compound containing a hydroxyl group or a group which is converted, after polymerization, into a hydroxyl group, e.g. by hydrolysis, oxidation, hydrogenation or hydration. Olefins preferred are octadecene, hexadecene and tetradecene, and mixtures such as obtained by cracking paraffin wax. The other monomer may be allyl or propargyl alcohol, a vinylhalide such as the chloride, or vinyl acetate, propionate, butyrate or benzoate. Specified alkyl esters of boric acid are trimethyl, triethyl, tripropyl and tributyl borates. The products may be used as described in Specification 829,635, in lubricating oil and fuel compositions.
Priority Applications (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| BE564374D BE564374A (en) | 1957-02-01 | ||
| NL224478D NL224478A (en) | 1957-02-01 | ||
| NL102463D NL102463C (en) | 1957-02-01 | ||
| GB366057A GB829634A (en) | 1957-02-01 | 1957-02-01 | Esters of polymeric hydroxyl compounds and boric acid |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB366057A GB829634A (en) | 1957-02-01 | 1957-02-01 | Esters of polymeric hydroxyl compounds and boric acid |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB829634A true GB829634A (en) | 1960-03-02 |
Family
ID=9762517
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB366057A Expired GB829634A (en) | 1957-02-01 | 1957-02-01 | Esters of polymeric hydroxyl compounds and boric acid |
Country Status (3)
| Country | Link |
|---|---|
| BE (1) | BE564374A (en) |
| GB (1) | GB829634A (en) |
| NL (2) | NL224478A (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0032572A1 (en) * | 1980-01-11 | 1981-07-29 | Hoechst Aktiengesellschaft | Process for the preparation of a polyvinyl alcohol complex compound, and polyvinylalcohol complex compound so prepared |
| EP0069301A1 (en) * | 1981-07-03 | 1983-01-12 | Hoechst Aktiengesellschaft | Process for the preparation of a polyvinyl alcohol complex compound, and the polyvinyl alcohol complex compound so prepared |
| EP0592240A2 (en) * | 1992-10-08 | 1994-04-13 | Sumitomo Chemical Company, Limited | Method for rendering resins compatible and composition comprising such compatibilized resins |
| US5616649A (en) * | 1993-10-07 | 1997-04-01 | Sumitomo Chemical Company, Limited | Method for compatibilizing resins with each other and resin composition comprising resins compatibilized with each other, obtained by said method |
| CN115960654A (en) * | 2021-10-11 | 2023-04-14 | 兰州大学 | Additive with high dispersibility and hydrolytic stability and capable of reducing friction coefficient of lubricating oil and improving extreme pressure load and preparation method thereof |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1151933B (en) * | 1960-07-11 | 1963-07-25 | Licentia Gmbh | Process for the production of molded articles or coatings from boron-modified epoxy resins |
-
0
- BE BE564374D patent/BE564374A/xx unknown
- NL NL102463D patent/NL102463C/xx active
- NL NL224478D patent/NL224478A/xx unknown
-
1957
- 1957-02-01 GB GB366057A patent/GB829634A/en not_active Expired
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0032572A1 (en) * | 1980-01-11 | 1981-07-29 | Hoechst Aktiengesellschaft | Process for the preparation of a polyvinyl alcohol complex compound, and polyvinylalcohol complex compound so prepared |
| US4331781A (en) | 1980-01-11 | 1982-05-25 | Hoechst Aktiengesellschaft | Process for the preparation of a polyvinyl alcohol complex compound in the presence of an organic boric acid derivative |
| EP0069301A1 (en) * | 1981-07-03 | 1983-01-12 | Hoechst Aktiengesellschaft | Process for the preparation of a polyvinyl alcohol complex compound, and the polyvinyl alcohol complex compound so prepared |
| EP0592240A2 (en) * | 1992-10-08 | 1994-04-13 | Sumitomo Chemical Company, Limited | Method for rendering resins compatible and composition comprising such compatibilized resins |
| EP0592240A3 (en) * | 1992-10-08 | 1994-10-26 | Sumitomo Chemical Co | Method for rendering resins compatible and composition comprising such compatibilized resins. |
| US5498664A (en) * | 1992-10-08 | 1996-03-12 | Sumitomo Chemical Company, Limited | Method for compatibilizing resins with each other and resin composition comprising resins compatibilized with each other, obtained by said method |
| US5616649A (en) * | 1993-10-07 | 1997-04-01 | Sumitomo Chemical Company, Limited | Method for compatibilizing resins with each other and resin composition comprising resins compatibilized with each other, obtained by said method |
| CN115960654A (en) * | 2021-10-11 | 2023-04-14 | 兰州大学 | Additive with high dispersibility and hydrolytic stability and capable of reducing friction coefficient of lubricating oil and improving extreme pressure load and preparation method thereof |
| CN115960654B (en) * | 2021-10-11 | 2024-05-17 | 兰州大学 | Additive with high dispersibility and hydrolytic stability and capable of reducing friction coefficient of lubricating oil and improving extreme pressure load and preparation method thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| BE564374A (en) | 1958-07-30 |
| NL224478A (en) | |
| NL102463C (en) | 1962-04-16 |
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