Process for producing organosilicon block-copolymers
专利摘要:
Thermoplastic, crystalline block copolymers are disclosed, each comprising a plurality of recurring units selected from the group consisting of those of the structural formulae F1 and F'1, and combinations thereof: F1: -A [SiR2 (GSiR2)aASiR2G'SiR2A]pSiR2(GSiR2)aASiR2(OSiR2)n] and F'1: -A [SiR2G'SiR2ASiR2(GSiR2)aA]pSiR2G'SiR2ASiR2(OSiR2)n] in which the symbols A, which are identical, represent linear or branched chain alkylene radicals having from 2 to 6 carbon atoms, or cyclohexylene radicals; the symbols R, which are identical or different, represent alkyl and halogenoalkyl radicals having from 1 to 5 carbon atoms, cycloalkyl and halogenocycloalkyl radicals having from 3 to 8 carbon atoms, aryl and halogenoaryl radicals having from 6 to 8 carbon atoms or cyanoalkyl radicals having from 3 to 4 carbon atoms; the symbols G, which are identical, represent linear or branched chain alkylene radicals having from 1 to 8 carbon atoms, divalent organic radicals corresponding to the formula F2: -CH2)xQTQ(CH2-x, in which the symbols Q, which are identical, represent one of the groups -O- and -OCO-, the -OCO- being bonded to T by the -CO- radical, the symbol T represents a monocyclic, divalent hydrocarbon radical having from 6 to 8 carbon atoms, or a divalent organic radical which has from 10 to 22 carbon atoms and consists of 2 hydrocarbon rings which are fused to one another or bonded together by a valence bond or by one of the groups of the formulae -O-, -CH2-, -C(CH3)2- and -Si(R'-2, wherein R' is an alkyl radical having from 1 to 3 carbon atoms, and the symbols x, which are identical represent 1, 2 or 3, or divalent hydrocarbon radicals corresponding to the formula F3: -CH2)bT(CH2)b, in which the symbol T has the measuring given for the formula F2 and the symbols b, which are identical, represent 0 or 1; s the symbols G', which are identical, have the meaning given above for G, except that they do not correspond to the formula F2; the symbols a, which are identical, represent 0 or 1; the symbols p represents any number ranging from 1 to 120; and the symbol n represents any number ranging from 1 to 1,500. 公开号:SU923372A3 申请号:SU792712805 申请日:1979-01-16 公开日:1982-04-23 发明作者:Баргэн Мишель;Прюдъомм Кристиан 申请人:Рон-Пуленк Эндюстри (Инофирма); IPC主号:
专利说明:
The goal is achieved by the fact that block copolymers are obtained by interaction in the presence of platinum СЯ, СНзСН5 СНзCHj CHj SNg (GS% CH2CH2Si - C - giCHaCHa - (GSi) % CHj catalyst-containing silicone compound of the formula CHE CH, SN3 CR5 with running reflux for 50 minutes. To the contents of the reactor, 27.18 g c1, HYDRO POLY dimethylsiloxane with a molecular weight of 8300 and 51 jA g toluene are added. In addition, 1 cm of the specified solution of chloroplatinic acid catalyst is added, the mixture is heated under reflux for 3 hours. The solution of the reaction product is poured. in 500 cm of absolute ethanol with vigorous stirring. The block copolymer is precipitated as fine particles, which are filtered, washed with ethanol and dried for an hour at a pressure of 20 mm Hg. The characteristic viscosity of the block copolymer at 20 ° C in chloroform is 0.3 dl / g. A portion of the obtained block copolymer is placed in a mold and heated at a pressure of 30 bar for 10 minutes. The obtained rubber plates have the following mechanical properties: Shore 73 hardness, tensile strength of b9 kg / cm, an elongation at break of 555, tear strength of 21 kg / cm, melting point 130-135 ° C. At a temperature, ° С: 20; 100-, 110 and 120 modulus of elasticity has values, kg / cm: 1, 2-10; 5 if-10 and 2.8-10 respectively. Example 3-12.5 g of bis-1, - (dimethylvinylsilyl) -methoxybenzolol, 7.18 g (0.037 mol) of bis-1, - (dimethylsilyl) (8DC5), CH2O are loaded into the glass solution described in example 1. - / OSYagvNSKz) a12SNg81 (SNZ), §1 (SNS) FROM uchgg ;, / vss / jc Si (CH5) gCM20- / -OCH2Si (CH5) 2CH2CH2Si (CH3) 2foSi (cai3) mL if Jeel Example k. A glass reactor described in example 1 was charged with 8.8A g {0, mol) 1- {vinyl dimethyl-silyl) (dimethylsilyl) -benzene, 0.76 g (0.0031 mol) bis-1, 4- (vinyldimethylsilyl) benzene; 28.8 g of toluene. With stirring, the mixture is heated in a stream of nitrogen to, then the heating is stopped and 0.15 cm of the catalyst-solution of chloroplatinic acid is added, then the heating is turned on again and the reaction mass is heated at the boiling point of toluene in tebenzene and 59.2 g of toluene, while stirring the reaction the mixture is heated in a stream of nitrogen to, then the heating is stopped and 1 cm of the catalyst, a solution of chloroplatinic acid, is added, the reaction mass is heated at boiling toluene under reflux for 35 minutes. To the obtained reaction product, 20.87 g of cL, t-dihydropolymethylsiloxane with a molecular weight of 5100 and 35.5 g of toluene are added, in addition, 0.2 of the specified catalyst is added. The resulting mixture is heated under reflux for 6 hours, the resulting block copolymer solution is applied in a thin layer onto a glass plate, the layer has a thickness of 0.5 mm. Then this plate is heated to 100 ° C at a pressure of 15 mm Hg, Art. within 1 hour The film obtained on the plate is cut into pieces, which are placed in molds, where they are kept for 15 1H at 160 ° C and pressure of 15 bar. As a result, rubber plates are formed which, after heat treatment at 80 ° C for 2 hours, have the following mechanical properties: Shore 77 hardness, tensile strength 70 kg / cm, an elongation at break 390, melting point 100-110 ° C. The characteristic viscosity of the block copolymer in chloroform is 0, i. dl / g The block copolymer has a formula 30 min. To the product obtained, 28.73 rdl, l-dihydropolymethylsiloxane with a molecular weight of 9300 and 60.8 g of toluene and 0.8 cm of the indicated catalyst solution are added. The mixture was heated under reflux for 5 hours. The solution of the obtained block copolymer was poured into 600 cm of absolute ethanol with vigorous stirring. The block copolymer is precipitated as white flakes. The flakes are crushed, washed with 700 cm of absolute ethanol and dried for 8 hours at a pressure of 15 mm Hg. The block copolymer powder is placed in a mold and heated at the bar for 10 minutes. The resulting plates have the following mechanical properties; breaking strength 600, strength - | cH2CH2fsi (CH3) (CH3) 2CH2CH2, ggi (CH3) (CH3) 2 jSample 5- 6.5 g (0.015 mol) of bis-4- (vinyldimethylsilyl) methoxyphenyl-2, 2- Propaia, 2.0 g (0.01 mol) of bis-, k- (dimethylsilyl) -benzene and 25 g of dry toluene, the mass is heated gradually with stirring under a stream of nitrogen. Then the heating is turned off and 0.3 cm of the catalyst of example 1 is added, the reaction mixture is refluxed for 30 minutes. Then 2b, 2b g of cL, -dihydropolydimethylsiloxane with a molecular weight of 5100 and 55 g of toluene and 0.16 cm of the catalyst solution are added. The reaction mixture is heated for 7 hours at 110 ° C, the resulting block copolymer solution is applied - {cH2CH2fgHc H5) gCm20-Vc (CH3) Si (CH3) 3C R2CH2 SKcHslgCHaO) g- (osH2 8g (CH3), CH2CH251 (CH3) 2 oVXH3) Example 6. 57.91 g (0.13 mol) bis are loaded into the glass reactor described in Example 1 -2; 2- ((vinyldimethylsilane) -methoxyphenyl) propane, 23.82 g (0.12 mol) of bis-1, - (diethylsilyl) -benzene and g of toluol. The contents of the reactor are stirred in a stream of nitrogen and gradually raise the temperature to, then the heating is turned off and k cm of the catalyst — a solution of the platinum chloride native acid of Example 1 is added. The reaction mass is stirred at reflux at a low boiling point of toluene for kk min, then 122, A8 g of cL, u) -dihydropolydimethyl siloxane with a molecular weight of 8600 and 230 g of toluene. 9233.5272 at 18 kg / cm tear, melting point. The characteristic viscosity of a block copolymer with chloroform is 0.57 DL / g. The block copolymer has the following formula: on a glass plate with a layer thickness of 0.5 mm. The plate is heated at 100 ° C for 1 h at a pressure of 15 mm Hg. The rubber film obtained on the Plate is cut into pieces, which are placed in a mold and heated at 170 ° / 15 bar for 15 minutes, then the resulting plate is removed from the mold and maintained at 80 ° C for 24 hours. The mechanical characteristics of these plates: hardness Shora 52, tensile strength 39 kg / cm | elongation at break, tear strength 12 kg / cm, melting point. The block copolymer is of the formula. The reaction mixture is refluxed for 5.5 m. The solution of the obtained copolymer is poured into 2 liters of absolute ethanol, the copolymer precipitates as white particles, which are filtered, washed with absolute ethanol and dried at 100 ° C for 2 h, with a pressure of 15 mm Hg. The resulting powder is placed in a mold and heated at 190 / / 30 bar for 20 minutes, rubber plates are obtained, which are thermally treated for 2 hours at 80 ° C. The plates have the following physicomechanical indicators; Wopy hardness 7b, tensile strength 93 kg / cm% breaking strength 580, tear strength 30 kg / cm, melting point 115 ° C. Characteristic viscosity at 20 ° C in chloroform 0.80 dlg. The modulus of elasticity at 2, about kg / cm at 2Q ° C - 1.1 / cm - | сН2СН2 й1 (С31з) 2СНгО-Л-С (СН5) 2 2 1m g з «2оO Example 7. In a glass reactor, capacity 250 cm according to Example 1, 21.67 g (0.05 mol) of bis-2, 2- i.- (vinyl dimethylsilyl) methoxyphenyl 3 -propane, 8.66 g (0, mol) bis-1, - (dimethylsilyl) -benzene and 75 g of toluene. The contents of the reactor, while stirring, are heated in a stream of nitrogen to 100 ° C, 1.3 cm of chloroplatinic acid solution is added and stirred at a low boil under reflux for 25 tWH. Then, 7.02 g of cL was added to the reaction mass, u was hydropolymethylsiloxane with a molecular weight of 1100, 12.5 g of toluene, and 0.2 cm of the indicated catalyst. The mixture is heated and refluxed for 1 h. 1сНгСЗг | -8ЦСН4 Жа0 з) 51 (G5) -) 8Isi gSNgSNg "IsNz sigo-s (Sn,;,. oCHaSUCHj.CSlaCH SHOH JoSKOHs) Example 8. 21.0 g (mol) of bis-2,2- (vinyl dimethylsilyl) -yutoxyphenyl) -propan, 8.85 g (0, mol) of bis-1, (dimethylsilyl) -benzene, 9b g of toluene, the contents of the reactor, while being stirred by stirring in a stream of nitrogen, are gradually heated up and 1.3 cm of chloroplatnic acid solution is added; the reaction mixture is boiled under reflux for tQ min, then 18, 01 g A, w-dihydropolid methylsiloxane with a molecular weight of 5100 and 22 g of toluene. The mixture is boiled under reflux for 5 hours, the block-sopo / millimeter solution is applied to a glass: 5 {-SUN; The data of elemental analysis and spectrophotometry confirm the preparation of a block copolymer of the formula The resulting copolymer solution was applied to a glass plate and heated at 100 ° C / 15 mm Hg. within 1 hour. The resulting rubber-like film is cut into pieces, which are placed in a mold that is heated at 170 ° C / 15 bar for 15 minutes, the resulting elastomer plate is heat treated, and then mechanical characteristics are measured: Shore 58 hardness , tensile strength 23b kg / cm, breaking elongation 599, tear strength. E kg / cm, melting point 120 ° C. The characteristic viscosity of the block copolymer at 20 ° C in chloroform is equal to O, dl / g. The data of elemental analysis and spectrophotometric analysis show that the block copolymer has the formula M, 5J plate thickness of 0.5 mm. The plate is heated at tOO ° C / 15 mm Hg. for 1 h, the obtained rubber film is cut into pieces, which are placed in a mold and heated in it at 170-180 0/30 bar. An elastomeric plate is obtained which, after heat treatment at 80 ° C 2 + .h, has the following physicomechanical characteristics: Shore hardness 51. strength. on a gap of 160 kg / cm, a tensile strength of 509, tear strength 57 kg / cm, melting point 120 ° C, According to the elemental and spectrophotometric analysis2 (and the block copolymer has the formula OSNg131 (cN3) „sn2CHN51 (cN3) - h) g (3 2 5 2 I gSNg81 (cN5 o“ KoNz) g sShg8 (eNe) sS NgSNg8CSN5) / yucMj) uSJ
权利要求:
Claims (1) [1] Claim A method for producing organosilicon block copolymers by reacting a vinyl-containing organosilicon compound with a hydride-containing organosilicon polymer in the presence of a platinum catalyst, characterized in that, in order to obtain block copolymers with enhanced thermomechanical characteristics, a compound of the general organosilicon compound is used as a vinyl-containing organosilicon compound formulas CH a CH 5 sn a SiCH 2 CH 2 T Si- (GSi ^ CH = CH 2 , sn 3 Jp CH 5 sn a Thus, according to the proposed method, thermoplastic block copolymers with improved thermomechanical characteristics are obtained, technical block copolymers according to the proposed method have an elastic modulus of 1-10 6 nLL-1 40 · n / m ^ · at 150 ° C, while the block copolymers according to the known method, having high initial mechanical characteristics, in the temperature zone above 110 ° C, the elastic modulus is much lower than 1 HO 6 n / mCh J0 sn 5 sn 3 en 5 CH 2 = CH-Si-Si- (CSi £ cH 2 CH 2 Si 'C 1 ss 5 ss 5 ss 3 CH 2 O _ ^ - CNN - ^) founded g -, VNIIIPI Order 2628/79 using ct, <jU-dihydropoly siloxane of the formula as a hydride-containing organosilicon polymer HSi (CH3) 2 -foSHCH5) 2 ^ H where η = 14.3-125.
类似技术:
公开号 | 公开日 | 专利标题 SU923372A3|1982-04-23|Process for producing organosilicon block-copolymers CA1295773C|1992-02-11|Organosilicon polymers US4902731A|1990-02-20|Organosilicon prepolymers US4877820A|1989-10-31|Cross-linked organosiloxane polymers EP0434848B1|1995-09-20|Polycarbonate-polydimethylsiloxane copolymer and method of production thereof JP5576552B2|2014-08-20|Hydroxy-terminated siloxane, polysiloxane-polycarbonate copolymer and process for producing the same Papetti et al.1966|A new series of organoboranes. VII. The preparation of poly‐m‐carboranylenesiloxanes EP3018165B1|2019-06-12|Polyorganosiloxane compound, method for preparing same, and copolycarbonate resin comprising same US4563514A|1986-01-07|Curable polysilarylene-polysiloxane copolymers KR101663555B1|2016-10-10|Thermoplastic copolymer resin having excellent transparency and flame-retardancy and method for preparing the same US5041514A|1991-08-20|Polymeric reaction products of biphenols and organosilicon materials and method for making US4213914A|1980-07-22|Ethylenic silicon compounds and thermoplastic elastomers obtained therefrom US4595732A|1986-06-17|Siloxane imide diols and siloxane imide organic block polymers obtained therefrom EP0282927B1|1997-06-18|Cross-linked organosiloxane polymers US5124423A|1992-06-23|Process for preparing organosilicon polymers US5260377A|1993-11-09|Crosslinkable carbosilane polymer formulations GB2152069A|1985-07-31|Ionically cross-linked siloxane polymers US4275184A|1981-06-23|Ethylenic silicon compounds and thermoplastic elastomers obtained therefrom JPH073030A|1995-01-06|Organosilicon polymer US5124375A|1992-06-23|Process for preparing organosilicon prepolymers and polymers FR2562080A1|1985-10-04|NORBORNANE CARBOXIMIDE COMPOSITION AND PROCESS FOR PRODUCING THE SAME EP0612785A2|1994-08-31|Epoxy-capped branched silicones and copolymers thereof KR102115799B1|2020-05-28|Polysiloxane-polycarbonate copolymer having improved transparency and low temperature impact resistance and method for preparing the same US3579607A|1971-05-18|Polyester-substituted organosilicon compositions US5512376A|1996-04-30|Nonpolar polymers comprising antiplasticizers
同族专利:
公开号 | 公开日 NL7900301A|1979-07-18| FR2414519B1|1980-07-04| CH636365A5|1983-05-31| DE2901514A1|1979-07-19| JPS6315299B2|1988-04-04| IT1110821B|1986-01-06| US4233427A|1980-11-11| GB2012297A|1979-07-25| IT7919342D0|1979-01-16| JPS54108000A|1979-08-24| BE873479A|1979-07-16| FR2414519A1|1979-08-10| GB2012297B|1982-06-30|
引用文献:
公开号 | 申请日 | 公开日 | 申请人 | 专利标题 US3249580A|1962-07-25|1966-05-03|Dow Corning|Air-curing organosilicon block copolymers containing polysilane blocks and organosilicon blocks| US3162663A|1963-01-10|1964-12-22|Dow Corning|Silethylenesilarylenes and siloxane derivatives thereof| DE1645651A1|1965-03-08|1970-09-17|Wacker Chemie Gmbh|Process for the preparation of polysilarylene siloxanes| NL182085C|1974-10-01|1988-01-04|Rhone Poulenc Ind|PROCESS FOR THE PREPARATION OF THERMOPLASTIC SILICON ORGANIC ELASTOMERS, AND FORMED PRODUCT, WHICH COMPRISES WHOLE OR PART| FR2362183B1|1976-08-17|1979-03-02|Rhone Poulenc Ind|EP0099432B1|1982-07-21|1987-01-07|Toray Industries, Inc.|Permselective membrane| FR2605326A1|1986-10-20|1988-04-22|Rhone Poulenc Multi Tech|POTENTIALLY ADHESIVE COMPOSITION ELECTRICALLY CONDUCTIVE.| FR2606784B1|1986-11-14|1989-03-03|Rhone Poulenc Multi Tech|ELECTRICALLY CONDUCTIVE POTENTIALLY ADHESIVE COMPOSITION| US4916038A|1987-05-05|1990-04-10|Hughes Aircraft Company|Substituted aromatic silane compounds and method for preparation of same| US4778871A|1987-08-25|1988-10-18|The United States Of America As Represented By The Secretary Of The Navy|High temperature insulators| JPH0345629A|1989-07-14|1991-02-27|Shin Etsu Chem Co Ltd|Organopolysiloxane polymer or copolymer and preparation thereof| FR2661683A1|1990-05-02|1991-11-08|Rhone Poulenc Chimie|MATERIAL CONTROLLED DELIVERY SYSTEM COMPRISING A DISPERSE HYDROSOLUBLE ACTIVE PRINCIPLE IN A MATRIX CONSISTING OF A THERMOPLASTIC SILICONE COPOLYMER| DE69427275T2|1993-12-28|2001-10-25|Kanegafuchi Chemical Ind|Silicon containing polymer, method of manufacture and monomer| IT1265461B1|1993-12-29|1996-11-22|Ausimont Spa|FLUOROELASTOMERS INCLUDING MONOMERIC UNITS ARISING FROM A BIS-OLEPHINE| IT1273608B|1995-04-28|1997-07-08|Ausimont Spa|FLUOROELASTOMERS SUBSTANTIALLY FREE OF POLAR TERMINALS AND RELATED PREPARATION PROCESS| AT191489T|1995-06-22|2000-04-15|Yuri Gudimenko|SURFACE MODIFICATION OF POLYMERS AND CARBONATED MATERIALS| JP3476283B2|1995-08-17|2003-12-10|富士通株式会社|Substrate flattening material and substrate flattening method using the same| IT1286042B1|1996-10-25|1998-07-07|Ausimont Spa|O-RINGS FROM VULCANIZABLE FLUOROELASTOMERS BY IONIC WAY| EP1007998A1|1997-02-11|2000-06-14|Massachusetts Institute Of Technology|Polymeric photonic band gap materials| AU4967499A|1998-07-02|2000-01-24|Massachusetts Institute Of Technology|Periodic porous and relief nanostructured articles| IT1318488B1|2000-04-21|2003-08-25|Ausimont Spa|FLUOROVINYLETERS AND POLYMERS THAT CAN BE OBTAINED.| IT1318487B1|2000-04-21|2003-08-25|Ausimont Spa|FLUORO-ELASTOMERS.| US7534845B2|2000-04-21|2009-05-19|Solvay Solexis S.P.A.|Fluorovinyl ethers and polymers obtainable therefrom| DE10030686A1|2000-06-23|2002-02-07|Wacker Chemie Gmbh|Polyimide silicone resin derived from diamine including diaminopolysiloxane and acid dianhydride, for, e.g., prevention of corrosion of liquid-crystal display panel electrodes, has specified amount of siloxane residual group| AU1875002A|2000-07-06|2002-01-21|Massachusetts Inst Technology|Photoactivated drug therapy| ITMI20011059A1|2001-05-22|2002-11-22|Ausimont Spa|FLUOROELASTOMERIC COMPOSITIONS| ITMI20011062A1|2001-05-22|2002-11-22|Ausimont Spa|FLUOROELASTOMERIC COMPOSITIONS| ITMI20011060A1|2001-05-22|2002-11-22|Ausimont Spa|FLUOROELASTOMERIC COMPOSITIONS| ITMI20012164A1|2001-10-18|2003-04-18|Ausimont Spa|FLUORO-ELASTOMERS| ITMI20020598A1|2002-03-22|2003-09-22|Ausimont Spa|VULCANIZABLE FLUOROELASTOMERS| ITMI20040830A1|2004-04-27|2004-07-27|Solvay Solexis Spa|VULCANIZABLE FLUOROELASTOMERS| ITMI20041251A1|2004-06-22|2004-09-22|Solvay Solexis Spa|PERFLUOROELASTOMER GEL| ITMI20041253A1|2004-06-22|2004-09-22|Solvay Solexis Spa|FLUOROELASTOMER GEL| ITMI20041573A1|2004-07-30|2006-01-31|Solvay Solexis Spa|FLUORO-ELASTOMERS| US8242210B2|2007-08-29|2012-08-14|Solvay Solexis S.P.A.|fluoroelastomeric compositions| KR101643423B1|2007-11-22|2016-07-27|솔베이 스페셜티 폴리머스 이태리 에스.피.에이.|Vulcanisable fluoroelastomeric compositions| EP2065441A1|2007-11-30|2009-06-03|Solvay Solexis S.p.A.|Fluoroelastomer composition| US8263708B2|2008-12-05|2012-09-11|Solvay Solexis S.P.A.|Vulcanizedfluoroelastomer sealing articles| EP2194094A1|2008-12-08|2010-06-09|Solvay Solexis S.p.A.|fluoroelastomer composition| WO2011073344A1|2009-12-18|2011-06-23|Solvay Solexis S.P.A.|Method for manufacturing fluoroelastomers| TWI523900B|2010-07-20|2016-03-01|首威索勒希斯股份有限公司|Fluoroelastomer composition| WO2012049093A1|2010-10-15|2012-04-19|Solvay Specialty Polymers Italy S.P.A.|Fluoroelastomers| CN103370346B|2010-12-20|2016-12-14|索尔维特殊聚合物意大利有限公司|low viscosity fluoroelastomer| EP2705061B1|2011-05-03|2017-02-01|Solvay Specialty Polymers Italy S.p.A.|Method for manufacturing fluoroelastomers| CN103890021B|2011-06-09|2016-03-23|索尔维特殊聚合物意大利有限公司|Hyperbranched fluoroelastomer additive| JP6530191B2|2011-08-17|2019-06-12|ソルベイ スペシャルティ ポリマーズ イタリー エス.ピー.エー.|Milling method| EP2797677A1|2011-12-27|2014-11-05|Dow Corning Corporation|High free volume siloxane compositions useful as membranes| CN105358591A|2013-06-28|2016-02-24|索尔维特殊聚合物意大利有限公司|Fluoroelastomers| CN108290985B|2015-09-18|2021-02-19|索尔维特殊聚合物意大利有限公司|Fluoroelastomer composition| KR20180093256A|2015-12-14|2018-08-21|솔베이 스페셜티 폴리머스 이태리 에스.피.에이.|Fluoroelastomer composition| WO2018064543A1|2016-09-30|2018-04-05|Dow Corning Corporation|Bridged silicone resin, film, electronic device and related methods| TWI742160B|2016-09-30|2021-10-11|美商道康寧公司|Bridged silicone resin, film, electronic device and related methods| RU2631111C1|2016-11-03|2017-09-19|Федеральное государственное бюджетное учреждение науки Институт элементоорганических соединений им. А.Н. Несмеянова Российской академии наук |Method for producing siloxane block copolymers| WO2019155073A1|2018-02-12|2019-08-15|Solvay Specialty Polymers Italy S.P.A.|Fluoroelastomer curable composition| US20220002505A1|2018-10-31|2022-01-06|Solvay Specialty Polymers Italy S.P.A.|Curable composition of elastomers| EP3941974A1|2019-03-20|2022-01-26|Solvay Specialty Polymers Italy S.p.A.|Fluoroelastomer composition| CN114126862A|2019-07-17|2022-03-01|索尔维特殊聚合物意大利有限公司|Composite material comprising polyamide and fluoroelastomer|
法律状态:
优先权:
[返回顶部]
申请号 | 申请日 | 专利标题 FR7801048A|FR2414519B1|1978-01-16|1978-01-16| 相关专利
Sulfonates, polymers, resist compositions and patterning process
Washing machine
Washing machine
Device for fixture finishing and tension adjusting of membrane
Structure for Equipping Band in a Plane Cathode Ray Tube
Process for preparation of 7 alpha-carboxyl 9, 11-epoxy steroids and intermediates useful therein an
国家/地区
|