GB1058385A - Organosilicon polymer compositions - Google Patents
Organosilicon polymer compositionsInfo
- Publication number
- GB1058385A GB1058385A GB3352764A GB3352764A GB1058385A GB 1058385 A GB1058385 A GB 1058385A GB 3352764 A GB3352764 A GB 3352764A GB 3352764 A GB3352764 A GB 3352764A GB 1058385 A GB1058385 A GB 1058385A
- Authority
- GB
- United Kingdom
- Prior art keywords
- hydrocarbon
- radical
- polyethers
- unsaturated
- hydrogen
- 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
- 239000000203 mixture Substances 0.000 title abstract 3
- 229920001558 organosilicon polymer Polymers 0.000 title 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract 6
- 229920000570 polyether Polymers 0.000 abstract 5
- 239000004215 Carbon black (E152) Chemical group 0.000 abstract 4
- 229930195733 hydrocarbon Chemical group 0.000 abstract 4
- 150000002430 hydrocarbons Chemical group 0.000 abstract 4
- 229910052739 hydrogen Inorganic materials 0.000 abstract 4
- 239000001257 hydrogen Substances 0.000 abstract 4
- -1 organic fibres Substances 0.000 abstract 4
- 150000002924 oxiranes Chemical class 0.000 abstract 4
- 229910052710 silicon Inorganic materials 0.000 abstract 3
- 239000010703 silicon Substances 0.000 abstract 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 abstract 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 abstract 2
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 abstract 2
- 125000004423 acyloxy group Chemical group 0.000 abstract 2
- 239000003513 alkali Substances 0.000 abstract 2
- 125000005529 alkyleneoxy group Chemical group 0.000 abstract 2
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 abstract 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 2
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 abstract 2
- 239000000945 filler Substances 0.000 abstract 2
- 150000005826 halohydrocarbons Chemical class 0.000 abstract 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 2
- 229910052760 oxygen Inorganic materials 0.000 abstract 2
- 239000001301 oxygen Substances 0.000 abstract 2
- 239000000049 pigment Substances 0.000 abstract 2
- 229920000642 polymer Polymers 0.000 abstract 2
- 230000000379 polymerizing effect Effects 0.000 abstract 2
- 239000000377 silicon dioxide Substances 0.000 abstract 2
- 101100386311 Arabidopsis thaliana DAPB3 gene Proteins 0.000 abstract 1
- 101150076189 CRR1 gene Proteins 0.000 abstract 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 1
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 abstract 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 239000005909 Kieselgur Substances 0.000 abstract 1
- 239000004721 Polyphenylene oxide Substances 0.000 abstract 1
- ACIAHEMYLLBZOI-ZZXKWVIFSA-N Unsaturated alcohol Chemical compound CC\C(CO)=C/C ACIAHEMYLLBZOI-ZZXKWVIFSA-N 0.000 abstract 1
- 125000003342 alkenyl group Chemical group 0.000 abstract 1
- 150000001412 amines Chemical class 0.000 abstract 1
- 239000010425 asbestos Substances 0.000 abstract 1
- 125000004429 atom Chemical group 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 239000006229 carbon black Substances 0.000 abstract 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 239000007799 cork Substances 0.000 abstract 1
- 239000012975 dibutyltin dilaurate Substances 0.000 abstract 1
- 239000011521 glass Substances 0.000 abstract 1
- 239000001023 inorganic pigment Substances 0.000 abstract 1
- 239000012860 organic pigment Substances 0.000 abstract 1
- AHHWIHXENZJRFG-UHFFFAOYSA-N oxetane Chemical compound C1COC1 AHHWIHXENZJRFG-UHFFFAOYSA-N 0.000 abstract 1
- 125000005702 oxyalkylene group Chemical group 0.000 abstract 1
- 229920001451 polypropylene glycol Polymers 0.000 abstract 1
- 239000004810 polytetrafluoroethylene Substances 0.000 abstract 1
- 229920001343 polytetrafluoroethylene Polymers 0.000 abstract 1
- 239000012255 powdered metal Substances 0.000 abstract 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
- CAEWJEXPFKNBQL-UHFFFAOYSA-N prop-2-enyl carbonochloridate Chemical compound ClC(=O)OCC=C CAEWJEXPFKNBQL-UHFFFAOYSA-N 0.000 abstract 1
- 239000010453 quartz Substances 0.000 abstract 1
- 239000000376 reactant Substances 0.000 abstract 1
- 229910052895 riebeckite Inorganic materials 0.000 abstract 1
- 125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 abstract 1
- 125000003808 silyl group Chemical group [H][Si]([H])([H])[*] 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
- 125000001302 tertiary amino group Chemical group 0.000 abstract 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 abstract 1
- KSBAEPSJVUENNK-UHFFFAOYSA-L tin(ii) 2-ethylhexanoate Chemical compound [Sn+2].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O KSBAEPSJVUENNK-UHFFFAOYSA-L 0.000 abstract 1
- 229930195735 unsaturated hydrocarbon Natural products 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1
- 239000002023 wood Substances 0.000 abstract 1
Classifications
-
- 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
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/32—Polymers modified by chemical after-treatment
- C08G65/329—Polymers modified by chemical after-treatment with organic compounds
- C08G65/331—Polymers modified by chemical after-treatment with organic compounds containing oxygen
- C08G65/332—Polymers modified by chemical after-treatment with organic compounds containing oxygen containing carboxyl groups, or halides, or esters thereof
- C08G65/3322—Polymers modified by chemical after-treatment with organic compounds containing oxygen containing carboxyl groups, or halides, or esters thereof acyclic
-
- 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
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/0834—Compounds having one or more O-Si linkage
- C07F7/0838—Compounds with one or more Si-O-Si sequences
- C07F7/0872—Preparation and treatment thereof
- C07F7/0876—Reactions involving the formation of bonds to a Si atom of a Si-O-Si sequence other than a bond of the Si-O-Si linkage
- C07F7/0878—Si-C bond
- C07F7/0879—Hydrosilylation reactions
-
- 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
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/0834—Compounds having one or more O-Si linkage
- C07F7/0892—Compounds with a Si-O-N linkage
-
- 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
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/18—Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages
-
- 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
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/04—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers only
- C08G65/22—Cyclic ethers having at least one atom other than carbon and hydrogen outside the ring
-
- 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
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/32—Polymers modified by chemical after-treatment
- C08G65/329—Polymers modified by chemical after-treatment with organic compounds
- C08G65/336—Polymers modified by chemical after-treatment with organic compounds containing silicon
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- General Chemical & Material Sciences (AREA)
- Polyethers (AREA)
Abstract
The invention comprises a composition consisting of (I) a silicon containing polyether in which (A) the polymer units consist essentially of oxyalkylene units of formula-O(CRR1)m-, wherein m is 1 to 5, each of R and R1 is a hydrogen, hydrocarbon ether, halo-hydrocarbon or -XSi(R11)n(Y)3- n radical in which X is a divalent radical free from acetylenic unsaturation composed of carbon and hydrogen and, optionally, oxygen, the oxygen being in the form of COH, C-O-, or -O-CO-, X being attached to the alkyleneoxy unit through a C-C bond, R11 is a monovalent hydrocarbon or halohydrocarbon radical, Y is hydrocarbonoxy, halohydrocarbonoxy, acyloxy, halogenated acyloxy, primary, secondary or tertiary amino or dihydrocarbyl-substituted isocyanoxy radical in which the substituents are hydrocarbon or halohydrocarbon radicals, n is 0, 1 or 2; there being not more than one silyl group attached to any one alkylene-oxy unit; and (B) the end-blocking groups are selected from hydrogen, monovalent hydrocarbon, halohydrocarbon and -WXSi(R11)nY3- n, where W is a divalent radical selected from O, -O.CO.O-, -O.CO- and urethane, X, Y, R11 and n being as defined above; there being on average at least two Si atoms, and at least three Y groups per polymer molecule; and (II) a pigment of filler. Many X, Y, R, R1 and R11 radicals are specified. Suitable pigments and fillers are cork, organic fibres, wood, glass, powdered metals, quartz, oxides, carbonates, diatomaceous earth, silica, asbestos, polytetrafluoroethylene, carbon black and organic and inorganic pigments. The organo-silicon polyethers may be prepared by reacting Y3- nSiH(R11)n with polyethers containing C = C bonds in either the terminal or side groups; or by polymerizing silicon-containing epoxides with or without other epoxides. The unsaturated polyethers may be prepared by polymerizing an epoxide in the presence of an alcohol, at least one reactant containing a C = C bond; the polyethers may be modified to yield further unsaturation, e.g. by reacting with an unsaturated epoxide, acetylene or a substituted acetylene, epichlorohydrin and alkali, followed by an unsaturated alcohol, an alkenyl halide and alkali, an alkenyl alcoholate or, a compound of formula X1(O)x.CO.Cl wherein X1 is an unsaturated-hydrocarbon radical, and x is 0 or 1. The compositions may be cured with water or atmospheric moisture, optionally in the presence of an organo- or organosilicontitanate, stannous octoate, dibutyl tin dilaurate or an amine as catalyst. Typical examples describe (1) the reaction of polypropylene glycol and allylchloroformate to form CH2 = CHCH2O . CO . O(C3H6O(68CO . O. CH2CH = CH2 which is condensed with methyl hydrogen diacetoxysilane to yield (CH3CO2)2Si(CH3)(CH2)3 O.CO(C3H6O)68CO.O(CH2)3Si(CH3) (O2CCH3)2; in (4) the oxetane <FORM:1058385/C3/1> is copolymerized with tetrahydrofuran in the presence BF3-etherate; both products are mixed with silica and di-butyl tin dilaurate and cured by exposure to air.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US31229763A | 1963-09-30 | 1963-09-30 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1058385A true GB1058385A (en) | 1967-02-08 |
Family
ID=23210809
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB3352764A Expired GB1058385A (en) | 1963-09-30 | 1964-08-17 | Organosilicon polymer compositions |
Country Status (8)
| Country | Link |
|---|---|
| JP (1) | JPS4836960B1 (en) |
| AT (1) | AT260547B (en) |
| BE (1) | BE653701A (en) |
| CH (1) | CH491983A (en) |
| DE (1) | DE1495543A1 (en) |
| GB (1) | GB1058385A (en) |
| NL (2) | NL6407761A (en) |
| SE (1) | SE319306B (en) |
Cited By (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4837401A (en) * | 1984-12-12 | 1989-06-06 | Kanegafuchi Chemical Industry, Co., Ltd. | Curable polymer composition comprising organic polymer having silicon-contaiing reactive group |
| EP0368195A2 (en) * | 1988-11-07 | 1990-05-16 | OSi Specialties, Inc. | Silicone polyether copolymers and process for their preparation |
| EP0397036A2 (en) * | 1989-05-09 | 1990-11-14 | Asahi Glass Company Ltd. | Process for producing polyalkylene oxide derivatives |
| JPH03162414A (en) * | 1989-11-06 | 1991-07-12 | Union Carbide Chem & Plast Co Inc | Surface active agent comprising silicone/polyether copolymer and its manufacture |
| US5045571A (en) * | 1988-11-07 | 1991-09-03 | Union Carbide Chemicals And Plastics Technology Corporation | Silicone polyether copolymers and polyurethane foams prepared therefrom |
| EP0496109A2 (en) * | 1990-12-26 | 1992-07-29 | UNION CARBIDE CHEMICALS & PLASTICS TECHNOLOGY CORPORATION, Three Cristina Centre | A process for producing alkoxysilane-terminated polyethers |
| EP0714953A2 (en) | 1994-12-01 | 1996-06-05 | Dow Corning S.A. | Moisture curable compositions of silyl-modified polymers |
| EP0714925A2 (en) | 1994-12-01 | 1996-06-05 | Dow Corning S.A. | Silyl group-containing organic polymers |
| EP0718340A2 (en) | 1994-12-01 | 1996-06-26 | Dow Corning S.A. | Silyl group-containing organic polymers |
| EP0771855A2 (en) | 1995-11-02 | 1997-05-07 | Dow Corning Corporation | Crosslinked emulsions of pre-formed silicon-modified organic polymers |
| EP0867443A2 (en) * | 1997-03-25 | 1998-09-30 | Ivoclar Ag | Hydrolyzable and polymerizable oxetanesilanes |
| US20140256844A1 (en) * | 2009-07-24 | 2014-09-11 | Evonik Degussa Gmbh | Novel silicone polyether copolymers and process for preparation thereof |
| CN111704864A (en) * | 2019-07-19 | 2020-09-25 | 广州市高士实业有限公司 | Silane modified polyether sealant and preparation method and application thereof |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3408321A (en) * | 1965-06-14 | 1968-10-29 | Gen Electric | Moisture curable siloxy terminated polyethers |
| US3448072A (en) * | 1965-06-14 | 1969-06-03 | Gen Electric | Silylurethane terminated polyester compositions |
| US3441534A (en) * | 1966-01-03 | 1969-04-29 | Gen Electric | Curable compositions |
| US4312993A (en) * | 1979-09-10 | 1982-01-26 | Sws Silicones Corporation | Silylated polyethers |
| KR100578737B1 (en) * | 2003-06-25 | 2006-05-12 | 학교법인 포항공과대학교 | Preparation of star-shaped polymers containing reactive end groups and polymer composite film having low dielectric constant using the same |
| JP4523763B2 (en) * | 2003-06-26 | 2010-08-11 | コニシ株式会社 | Adhesive composition |
| DE102009042201A1 (en) | 2009-09-18 | 2011-04-14 | Bayer Materialscience Ag | Silane-containing polyethers |
| DE102009042190A1 (en) | 2009-09-18 | 2011-03-24 | Bayer Materialscience Ag | Silane-containing reactive diluents |
-
0
- NL NL128826D patent/NL128826C/xx active
-
1964
- 1964-06-02 JP JP3096364A patent/JPS4836960B1/ja active Pending
- 1964-06-26 SE SE786064A patent/SE319306B/xx unknown
- 1964-07-08 NL NL6407761A patent/NL6407761A/xx unknown
- 1964-07-14 CH CH925264A patent/CH491983A/en not_active IP Right Cessation
- 1964-08-17 GB GB3352764A patent/GB1058385A/en not_active Expired
- 1964-08-28 DE DE19641495543 patent/DE1495543A1/en active Pending
- 1964-09-10 AT AT779264A patent/AT260547B/en active
- 1964-09-29 BE BE653701D patent/BE653701A/xx unknown
Cited By (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4837401A (en) * | 1984-12-12 | 1989-06-06 | Kanegafuchi Chemical Industry, Co., Ltd. | Curable polymer composition comprising organic polymer having silicon-contaiing reactive group |
| EP0368195A2 (en) * | 1988-11-07 | 1990-05-16 | OSi Specialties, Inc. | Silicone polyether copolymers and process for their preparation |
| EP0368195A3 (en) * | 1988-11-07 | 1991-04-24 | OSi Specialties, Inc. | Silicone polyether copolymers and process for their preparation |
| US5045571A (en) * | 1988-11-07 | 1991-09-03 | Union Carbide Chemicals And Plastics Technology Corporation | Silicone polyether copolymers and polyurethane foams prepared therefrom |
| US5223583A (en) * | 1989-05-09 | 1993-06-29 | Asahi Glass Company Ltd. | Process for producing polyalkylene oxide derivatives |
| EP0397036A2 (en) * | 1989-05-09 | 1990-11-14 | Asahi Glass Company Ltd. | Process for producing polyalkylene oxide derivatives |
| EP0397036A3 (en) * | 1989-05-09 | 1991-03-13 | Asahi Glass Company Ltd. | Process for producing polyalkylene oxide derivatives |
| JPH0747630B2 (en) | 1989-11-06 | 1995-05-24 | ユニオン・カーバイド・ケミカルズ・アンド・プラスチツクス・カンパニー・インコーポレーテツド | Silicone polyether copolymer surfactant |
| JPH03162414A (en) * | 1989-11-06 | 1991-07-12 | Union Carbide Chem & Plast Co Inc | Surface active agent comprising silicone/polyether copolymer and its manufacture |
| EP0496109A3 (en) * | 1990-12-26 | 1992-11-25 | Union Carbide Chemicals & Plastics Technology Corporation, Three Cristina Centre | A process for producing alkoxysilane-terminated polyethers |
| EP0496109A2 (en) * | 1990-12-26 | 1992-07-29 | UNION CARBIDE CHEMICALS & PLASTICS TECHNOLOGY CORPORATION, Three Cristina Centre | A process for producing alkoxysilane-terminated polyethers |
| EP0714953A3 (en) * | 1994-12-01 | 1996-12-27 | Dow Corning Sa | Moisture curable compositions of silyl-modified polymers |
| EP0714925A2 (en) | 1994-12-01 | 1996-06-05 | Dow Corning S.A. | Silyl group-containing organic polymers |
| EP0718340A2 (en) | 1994-12-01 | 1996-06-26 | Dow Corning S.A. | Silyl group-containing organic polymers |
| EP0714953A2 (en) | 1994-12-01 | 1996-06-05 | Dow Corning S.A. | Moisture curable compositions of silyl-modified polymers |
| EP0718340A3 (en) * | 1994-12-01 | 1997-01-02 | Dow Corning Sa | Silyl group-containing organic polymers |
| EP0771855A2 (en) | 1995-11-02 | 1997-05-07 | Dow Corning Corporation | Crosslinked emulsions of pre-formed silicon-modified organic polymers |
| EP0867443A2 (en) * | 1997-03-25 | 1998-09-30 | Ivoclar Ag | Hydrolyzable and polymerizable oxetanesilanes |
| EP0867443A3 (en) * | 1997-03-25 | 2000-06-28 | Ivoclar Ag | Hydrolyzable and polymerizable oxetanesilanes |
| US20140256844A1 (en) * | 2009-07-24 | 2014-09-11 | Evonik Degussa Gmbh | Novel silicone polyether copolymers and process for preparation thereof |
| CN111704864A (en) * | 2019-07-19 | 2020-09-25 | 广州市高士实业有限公司 | Silane modified polyether sealant and preparation method and application thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| SE319306B (en) | 1970-01-12 |
| BE653701A (en) | 1965-03-29 |
| DE1495543A1 (en) | 1969-02-27 |
| NL128826C (en) | |
| NL6407761A (en) | 1965-03-31 |
| CH491983A (en) | 1970-06-15 |
| AT260547B (en) | 1968-03-11 |
| JPS4836960B1 (en) | 1973-11-08 |
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