GB1111603A - Reinforced poly(alkyl methacrylate) compositions - Google Patents
Reinforced poly(alkyl methacrylate) compositionsInfo
- Publication number
- GB1111603A GB1111603A GB652/66A GB65266A GB1111603A GB 1111603 A GB1111603 A GB 1111603A GB 652/66 A GB652/66 A GB 652/66A GB 65266 A GB65266 A GB 65266A GB 1111603 A GB1111603 A GB 1111603A
- Authority
- GB
- United Kingdom
- Prior art keywords
- alkyl
- reinforcing
- methacrylate
- agents
- reacting
- 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
- -1 poly(alkyl methacrylate Chemical compound 0.000 title abstract 10
- 239000000203 mixture Substances 0.000 title abstract 6
- 239000007822 coupling agent Substances 0.000 abstract 6
- 239000012744 reinforcing agent Substances 0.000 abstract 5
- 238000006116 polymerization reaction Methods 0.000 abstract 4
- UORVGPXVDQYIDP-UHFFFAOYSA-N borane Chemical compound B UORVGPXVDQYIDP-UHFFFAOYSA-N 0.000 abstract 3
- 239000003054 catalyst Substances 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 3
- 229920000642 polymer Polymers 0.000 abstract 3
- 239000000047 product Substances 0.000 abstract 3
- 230000003014 reinforcing effect Effects 0.000 abstract 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract 3
- 239000010456 wollastonite Substances 0.000 abstract 3
- 229910052882 wollastonite Inorganic materials 0.000 abstract 3
- RGOVHAJZSSODRY-UHFFFAOYSA-N 11-trimethoxysilylundecyl 2-methylprop-2-enoate Chemical compound CO[Si](OC)(OC)CCCCCCCCCCCOC(=O)C(C)=C RGOVHAJZSSODRY-UHFFFAOYSA-N 0.000 abstract 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 abstract 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 abstract 2
- 125000005599 alkyl carboxylate group Chemical group 0.000 abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 239000003795 chemical substances by application Substances 0.000 abstract 2
- RWGFKTVRMDUZSP-UHFFFAOYSA-N cumene Chemical compound CC(C)C1=CC=CC=C1 RWGFKTVRMDUZSP-UHFFFAOYSA-N 0.000 abstract 2
- 239000010433 feldspar Substances 0.000 abstract 2
- 229910052736 halogen Inorganic materials 0.000 abstract 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 2
- 229910052751 metal Inorganic materials 0.000 abstract 2
- 239000002184 metal Substances 0.000 abstract 2
- 239000000178 monomer Substances 0.000 abstract 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 abstract 2
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 abstract 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 abstract 1
- VCVAXEYHJAFRGM-UHFFFAOYSA-N 10-Undecenyl acetate Chemical compound CC(=O)OCCCCCCCCCC=C VCVAXEYHJAFRGM-UHFFFAOYSA-N 0.000 abstract 1
- GPHCMDOASQYDKS-UHFFFAOYSA-N 11-trichlorosilylundecyl acetate Chemical compound CC(=O)OCCCCCCCCCCC[Si](Cl)(Cl)Cl GPHCMDOASQYDKS-UHFFFAOYSA-N 0.000 abstract 1
- NYHNAERBYRFHRV-UHFFFAOYSA-N 18-trichlorosilyloctadecyl prop-2-enoate Chemical compound C(C=C)(=O)OCCCCCCCCCCCCCCCCCC[Si](Cl)(Cl)Cl NYHNAERBYRFHRV-UHFFFAOYSA-N 0.000 abstract 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 abstract 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 abstract 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 abstract 1
- 239000004342 Benzoyl peroxide Substances 0.000 abstract 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 abstract 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 abstract 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 abstract 1
- GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 abstract 1
- 229910019142 PO4 Inorganic materials 0.000 abstract 1
- 239000004793 Polystyrene Substances 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- XECAHXYUAAWDEL-UHFFFAOYSA-N acrylonitrile butadiene styrene Chemical compound C=CC=C.C=CC#N.C=CC1=CC=CC=C1 XECAHXYUAAWDEL-UHFFFAOYSA-N 0.000 abstract 1
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 abstract 1
- 239000004676 acrylonitrile butadiene styrene Substances 0.000 abstract 1
- 239000012190 activator Substances 0.000 abstract 1
- 125000003342 alkenyl group Chemical group 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 1
- 125000005250 alkyl acrylate group Chemical group 0.000 abstract 1
- 125000004448 alkyl carbonyl group Chemical group 0.000 abstract 1
- 125000002947 alkylene group Chemical group 0.000 abstract 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 abstract 1
- CNLWCVNCHLKFHK-UHFFFAOYSA-N aluminum;lithium;dioxido(oxo)silane Chemical compound [Li+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O CNLWCVNCHLKFHK-UHFFFAOYSA-N 0.000 abstract 1
- 150000001412 amines Chemical class 0.000 abstract 1
- 229960000892 attapulgite Drugs 0.000 abstract 1
- 150000007514 bases Chemical class 0.000 abstract 1
- 239000000440 bentonite Substances 0.000 abstract 1
- 229910000278 bentonite Inorganic materials 0.000 abstract 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 abstract 1
- 235000019400 benzoyl peroxide Nutrition 0.000 abstract 1
- 229910000085 borane Inorganic materials 0.000 abstract 1
- 229910010277 boron hydride Inorganic materials 0.000 abstract 1
- VNSBYDPZHCQWNB-UHFFFAOYSA-N calcium;aluminum;dioxido(oxo)silane;sodium;hydrate Chemical compound O.[Na].[Al].[Ca+2].[O-][Si]([O-])=O VNSBYDPZHCQWNB-UHFFFAOYSA-N 0.000 abstract 1
- 150000001722 carbon compounds Chemical class 0.000 abstract 1
- 238000005266 casting Methods 0.000 abstract 1
- 239000007795 chemical reaction product Substances 0.000 abstract 1
- 230000008878 coupling Effects 0.000 abstract 1
- 238000010168 coupling process Methods 0.000 abstract 1
- 238000005859 coupling reaction Methods 0.000 abstract 1
- 229910052906 cristobalite Inorganic materials 0.000 abstract 1
- GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 abstract 1
- KZHJGOXRZJKJNY-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Si]=O.O=[Al]O[Al]=O.O=[Al]O[Al]=O.O=[Al]O[Al]=O KZHJGOXRZJKJNY-UHFFFAOYSA-N 0.000 abstract 1
- 239000002612 dispersion medium Substances 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 abstract 1
- 239000011953 free-radical catalyst Substances 0.000 abstract 1
- 239000002223 garnet Substances 0.000 abstract 1
- 239000000499 gel Substances 0.000 abstract 1
- 239000003365 glass fiber Substances 0.000 abstract 1
- 239000010439 graphite Substances 0.000 abstract 1
- 229910002804 graphite Inorganic materials 0.000 abstract 1
- 239000005337 ground glass Substances 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 229910001385 heavy metal Inorganic materials 0.000 abstract 1
- 229910000271 hectorite Inorganic materials 0.000 abstract 1
- KWLMIXQRALPRBC-UHFFFAOYSA-L hectorite Chemical compound [Li+].[OH-].[OH-].[Na+].[Mg+2].O1[Si]2([O-])O[Si]1([O-])O[Si]([O-])(O1)O[Si]1([O-])O2 KWLMIXQRALPRBC-UHFFFAOYSA-L 0.000 abstract 1
- 229910001691 hercynite Inorganic materials 0.000 abstract 1
- PYGSKMBEVAICCR-UHFFFAOYSA-N hexa-1,5-diene Chemical group C=CCCC=C PYGSKMBEVAICCR-UHFFFAOYSA-N 0.000 abstract 1
- 150000002430 hydrocarbons Chemical group 0.000 abstract 1
- 125000001183 hydrocarbyl group Chemical group 0.000 abstract 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 abstract 1
- 229910052622 kaolinite Inorganic materials 0.000 abstract 1
- 239000007788 liquid Substances 0.000 abstract 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 abstract 1
- 229910052976 metal sulfide Inorganic materials 0.000 abstract 1
- 150000002739 metals Chemical class 0.000 abstract 1
- 239000010445 mica Substances 0.000 abstract 1
- 229910052618 mica group Inorganic materials 0.000 abstract 1
- 229910052901 montmorillonite Inorganic materials 0.000 abstract 1
- 229910052863 mullite Inorganic materials 0.000 abstract 1
- YCLVJBBBAQRAPA-UHFFFAOYSA-N octadec-17-enyl propanoate Chemical compound C(CC)(=O)OCCCCCCCCCCCCCCCCC=C YCLVJBBBAQRAPA-UHFFFAOYSA-N 0.000 abstract 1
- 150000002940 palladium Chemical class 0.000 abstract 1
- 229910052625 palygorskite Inorganic materials 0.000 abstract 1
- 235000021317 phosphate Nutrition 0.000 abstract 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 abstract 1
- 229910052697 platinum Inorganic materials 0.000 abstract 1
- 229920002285 poly(styrene-co-acrylonitrile) Polymers 0.000 abstract 1
- 229920000728 polyester Polymers 0.000 abstract 1
- 230000000379 polymerizing effect Effects 0.000 abstract 1
- 229920001296 polysiloxane Polymers 0.000 abstract 1
- 229920002223 polystyrene Polymers 0.000 abstract 1
- JUJWROOIHBZHMG-UHFFFAOYSA-N pyridine Substances C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 abstract 1
- 239000010453 quartz Substances 0.000 abstract 1
- 238000009877 rendering Methods 0.000 abstract 1
- 229920005989 resin Polymers 0.000 abstract 1
- 239000011347 resin Substances 0.000 abstract 1
- 229910000275 saponite Inorganic materials 0.000 abstract 1
- 150000004756 silanes Chemical class 0.000 abstract 1
- 239000000741 silica gel Substances 0.000 abstract 1
- 229910002027 silica gel Inorganic materials 0.000 abstract 1
- 229910052642 spodumene Inorganic materials 0.000 abstract 1
- 239000000126 substance Substances 0.000 abstract 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 abstract 1
- 239000004094 surface-active agent Substances 0.000 abstract 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 abstract 1
- 150000003568 thioethers Chemical class 0.000 abstract 1
- ZDHXKXAHOVTTAH-UHFFFAOYSA-N trichlorosilane Chemical compound Cl[SiH](Cl)Cl ZDHXKXAHOVTTAH-UHFFFAOYSA-N 0.000 abstract 1
- 239000005052 trichlorosilane Substances 0.000 abstract 1
- ULEFFCDROVNTRO-UHFFFAOYSA-N trimagnesium;disodium;dihydroxy(oxo)silane;iron(3+) Chemical compound [Na+].[Na+].[Mg+2].[Mg+2].[Mg+2].[Fe+3].[Fe+3].O[Si](O)=O.O[Si](O)=O.O[Si](O)=O.O[Si](O)=O.O[Si](O)=O.O[Si](O)=O.O[Si](O)=O.O[Si](O)=O ULEFFCDROVNTRO-UHFFFAOYSA-N 0.000 abstract 1
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 abstract 1
Classifications
-
- 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
- C08F292/00—Macromolecular compounds obtained by polymerising monomers on to inorganic materials
-
- 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
- C07F7/12—Organo silicon halides
-
- 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
- C07F7/1804—Compounds having Si-O-C linkages
-
- 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
- C07F7/1896—Compounds having one or more Si-O-acyl linkages
-
- 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
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/66—Arsenic compounds
-
- 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
- C08F2/00—Processes of polymerisation
- C08F2/44—Polymerisation in the presence of compounding ingredients, e.g. plasticisers, dyestuffs, fillers
-
- 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
- C08F20/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride, ester, amide, imide or nitrile thereof
- C08F20/02—Monocarboxylic acids having less than ten carbon atoms, Derivatives thereof
- C08F20/10—Esters
- C08F20/12—Esters of monohydric alcohols or phenols
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Engineering & Computer Science (AREA)
- Inorganic Chemistry (AREA)
- Materials Engineering (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US42384265A | 1965-01-06 | 1965-01-06 | |
US44578165A | 1965-04-05 | 1965-04-05 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1111603A true GB1111603A (en) | 1968-05-01 |
Family
ID=27026160
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB652/66A Expired GB1111603A (en) | 1965-01-06 | 1966-01-06 | Reinforced poly(alkyl methacrylate) compositions |
Country Status (9)
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2576309A1 (fr) * | 1984-12-05 | 1986-07-25 | Gen Electric | Procede de fabrication de compositions de silicones a fonction acrylique |
EP0368657A2 (en) * | 1988-11-11 | 1990-05-16 | Kuraray Co., Ltd. | Dental restorative material |
US5385973A (en) * | 1987-12-17 | 1995-01-31 | Vedril S.P.A. | Process for preparing flowable, stable and hardenable suspensions, and thus-obtained compositions |
EP2993200A1 (en) | 2014-09-02 | 2016-03-09 | Greenseal Chemicals NV | Thiol-acrylate based foam precursor composition |
WO2017036525A1 (en) | 2015-09-02 | 2017-03-09 | Greenseal Chemicals Nv | Thiol-acrylate based foam precursor composition |
WO2022029237A1 (en) * | 2020-08-05 | 2022-02-10 | Greenseal Nv | Method for obtaining an oxygen curable composition using a borane compound as oxygen scavenger |
Families Citing this family (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3700714A (en) * | 1971-06-24 | 1972-10-24 | Stephen B Hamilton | Curable compositions |
DE2655877A1 (de) * | 1976-12-09 | 1978-06-15 | Wacker Chemie Gmbh | Verfahren zum herstellen und verwendung von silanen |
JPS6017799B2 (ja) * | 1979-06-29 | 1985-05-07 | 信越化学工業株式会社 | 有機けい素化合物 |
US4281145A (en) * | 1980-04-02 | 1981-07-28 | General Electric Company | Process for producing alkoxylated silanes |
GB8405731D0 (en) * | 1984-03-05 | 1984-04-11 | Dow Corning Ltd | Preparation of organosiloxanes |
US4659851A (en) * | 1986-03-26 | 1987-04-21 | Dow Corning Corporation | Novel organosilicon compounds |
JPS63179881A (ja) * | 1987-01-19 | 1988-07-23 | Shin Etsu Chem Co Ltd | 有機けい素化合物 |
US5391677A (en) * | 1991-07-23 | 1995-02-21 | Shin-Etsu Chemical Co., Ltd. | Acrylic-functional organopolysiloxane and method for the preparation thereof |
DE4225309A1 (de) * | 1992-07-31 | 1994-02-03 | Roehm Gmbh | Suspension für die Herstellung gefüllter Gießharze |
WO2008093596A1 (ja) * | 2007-02-01 | 2008-08-07 | Kuraray Medical Inc. | 歯科用硬化性組成物 |
CN105152237A (zh) * | 2015-08-30 | 2015-12-16 | 常州市鼎日环保科技有限公司 | 一种凹凸棒基多孔超疏水性材料的制备方法 |
DE102016105525A1 (de) * | 2016-03-24 | 2017-09-28 | Blanco Gmbh + Co Kg | Aushärtbare Gießmasse für die Herstellung von Kunststoffformteilen und deren Verwendung |
CN112385562A (zh) * | 2020-11-09 | 2021-02-23 | 黄高卫 | 一种宠物狗用衣服 |
CN115043591B (zh) * | 2022-07-20 | 2023-05-12 | 西南科技大学 | 多孔微晶陶瓷及其制备方法 |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3317369A (en) * | 1961-04-07 | 1967-05-02 | Dow Corning | Acryloxyalkylsilane compositions and the fabrication of structures therewith |
US3227675A (en) * | 1963-05-01 | 1966-01-04 | Huber Corp J M | Silane-treated clay reinforced resin compositions |
-
1965
- 1965-04-05 US US445781A patent/US3427337A/en not_active Expired - Lifetime
- 1965-12-30 SE SE17011/65A patent/SE334471B/xx unknown
- 1965-12-31 BE BE674610D patent/BE674610A/xx unknown
-
1966
- 1966-01-04 IL IL24917A patent/IL24917A/xx unknown
- 1966-01-05 DE DE19661694574 patent/DE1694574A1/de active Pending
- 1966-01-06 GB GB652/66A patent/GB1111603A/en not_active Expired
- 1966-01-06 LU LU50213A patent/LU50213A1/xx unknown
- 1966-01-06 NL NL6600164A patent/NL6600164A/xx unknown
- 1966-01-07 AT AT03822/69A patent/AT285628B/de not_active IP Right Cessation
- 1966-01-07 AT AT12366A patent/AT281412B/de not_active IP Right Cessation
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2576309A1 (fr) * | 1984-12-05 | 1986-07-25 | Gen Electric | Procede de fabrication de compositions de silicones a fonction acrylique |
US5385973A (en) * | 1987-12-17 | 1995-01-31 | Vedril S.P.A. | Process for preparing flowable, stable and hardenable suspensions, and thus-obtained compositions |
EP0368657A2 (en) * | 1988-11-11 | 1990-05-16 | Kuraray Co., Ltd. | Dental restorative material |
EP0368657A3 (en) * | 1988-11-11 | 1991-04-03 | Kuraray Co., Ltd. | Dental restorative material |
EP2993200A1 (en) | 2014-09-02 | 2016-03-09 | Greenseal Chemicals NV | Thiol-acrylate based foam precursor composition |
WO2017036525A1 (en) | 2015-09-02 | 2017-03-09 | Greenseal Chemicals Nv | Thiol-acrylate based foam precursor composition |
US10875942B2 (en) | 2015-09-02 | 2020-12-29 | Greenseal Nv | Thiol-acrylate based foam precursor composition |
WO2022029237A1 (en) * | 2020-08-05 | 2022-02-10 | Greenseal Nv | Method for obtaining an oxygen curable composition using a borane compound as oxygen scavenger |
Also Published As
Publication number | Publication date |
---|---|
AT281412B (de) | 1970-05-25 |
NL6600164A (US06559137-20030506-C00047.png) | 1966-07-07 |
US3427337A (en) | 1969-02-11 |
BE674610A (US06559137-20030506-C00047.png) | 1966-06-30 |
SE334471B (US06559137-20030506-C00047.png) | 1971-04-26 |
DE1694574A1 (de) | 1972-03-16 |
LU50213A1 (US06559137-20030506-C00047.png) | 1966-07-06 |
AT285628B (de) | 1970-11-10 |
IL24917A (en) | 1969-11-30 |
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