NO309986B1 - Funksjonaliserte polyorganosiloksaner, fremgangsmÕte for fremstilling derav, og anvendelse derav - Google Patents

Funksjonaliserte polyorganosiloksaner, fremgangsmÕte for fremstilling derav, og anvendelse derav Download PDF

Info

Publication number: NO309986B1
Authority: NO; Norway
Prior art keywords: formula; linear; radical; branched; stated
Prior art date: 1994-11-18

Application number

NO972248A

Other languages

English (en)

Norwegian (no)

Other versions

NO972248L (no

NO972248D0 (no

Inventor

Michel Gay

Philippe Jost

Michel Peignier

Christian Priou

Original Assignee

Rhone Poulenc Chimie

Priority date (The priority date 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 date listed.)

1994-11-18

Filing date

1997-05-16

Publication date

2001-04-30

Family has litigation

First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=9469088&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=NO309986(B1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.

1997-05-16 Application filed by Rhone Poulenc Chimie filed Critical Rhone Poulenc Chimie

1997-05-16 Publication of NO972248D0 publication Critical patent/NO972248D0/no

1997-07-18 Publication of NO972248L publication Critical patent/NO972248L/no

2001-04-30 Publication of NO309986B1 publication Critical patent/NO309986B1/no

Links

238000000034 method Methods 0.000 title claims description 33
230000008569 process Effects 0.000 title claims description 7
238000002360 preparation method Methods 0.000 title description 12
239000003054 catalyst Substances 0.000 claims description 29
BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Substances [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims description 26
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 25
238000006356 dehydrogenation reaction Methods 0.000 claims description 23
238000009833 condensation Methods 0.000 claims description 22
230000005494 condensation Effects 0.000 claims description 22
125000004469 siloxy group Chemical group [SiH3]O* 0.000 claims description 20
239000000203 mixture Substances 0.000 claims description 19
125000001424 substituent group Chemical group 0.000 claims description 18
239000001257 hydrogen Substances 0.000 claims description 17
229910052739 hydrogen Inorganic materials 0.000 claims description 17
125000000217 alkyl group Chemical group 0.000 claims description 16
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 14
238000006459 hydrosilylation reaction Methods 0.000 claims description 14
229910052697 platinum Inorganic materials 0.000 claims description 13
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 12
125000004432 carbon atom Chemical group C* 0.000 claims description 11
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 11
239000000376 reactant Substances 0.000 claims description 10
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 9
125000003545 alkoxy group Chemical group 0.000 claims description 9
229910052710 silicon Inorganic materials 0.000 claims description 9
239000010703 silicon Substances 0.000 claims description 9
150000001875 compounds Chemical class 0.000 claims description 8
229920001296 polysiloxane Polymers 0.000 claims description 8
229910052721 tungsten Inorganic materials 0.000 claims description 8
229910052727 yttrium Inorganic materials 0.000 claims description 8
239000004215 Carbon black (E152) Substances 0.000 claims description 7
229930195733 hydrocarbon Natural products 0.000 claims description 7
230000007246 mechanism Effects 0.000 claims description 7
229920002379 silicone rubber Polymers 0.000 claims description 7
125000002947 alkylene group Chemical group 0.000 claims description 6
125000004122 cyclic group Chemical group 0.000 claims description 6
125000003342 alkenyl group Chemical group 0.000 claims description 5
239000011248 coating agent Substances 0.000 claims description 5
-1 methoxy, ethoxy Chemical group 0.000 claims description 5
239000011541 reaction mixture Substances 0.000 claims description 5
229910010271 silicon carbide Inorganic materials 0.000 claims description 5
125000006273 (C1-C3) alkyl group Chemical group 0.000 claims description 4
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 4
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 claims description 4
230000015572 biosynthetic process Effects 0.000 claims description 4
230000007717 exclusion Effects 0.000 claims description 4
239000000945 filler Substances 0.000 claims description 4
125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 4
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
239000000377 silicon dioxide Substances 0.000 claims description 4
125000005369 trialkoxysilyl group Chemical group 0.000 claims description 4
239000007810 chemical reaction solvent Substances 0.000 claims description 3
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 3
229910052759 nickel Inorganic materials 0.000 claims description 3
230000001737 promoting effect Effects 0.000 claims description 3
125000003358 C2-C20 alkenyl group Chemical group 0.000 claims description 2
SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 claims description 2
229910018540 Si C Inorganic materials 0.000 claims description 2
CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 claims description 2
230000003213 activating effect Effects 0.000 claims description 2
125000005370 alkoxysilyl group Chemical group 0.000 claims description 2
125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims description 2
125000003118 aryl group Chemical group 0.000 claims description 2
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 2
125000002619 bicyclic group Chemical group 0.000 claims description 2
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
229920001577 copolymer Polymers 0.000 claims description 2
125000000596 cyclohexenyl group Chemical group C1(=CCCCC1)* 0.000 claims description 2
125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 2
150000002148 esters Chemical class 0.000 claims description 2
125000001033 ether group Chemical group 0.000 claims description 2
125000005842 heteroatom Chemical group 0.000 claims description 2
125000006038 hexenyl group Chemical group 0.000 claims description 2
229920005684 linear copolymer Polymers 0.000 claims description 2
230000000873 masking effect Effects 0.000 claims description 2
125000005358 mercaptoalkyl group Chemical group 0.000 claims description 2
125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
229910052763 palladium Inorganic materials 0.000 claims description 2
150000008117 polysulfides Polymers 0.000 claims description 2
BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 claims description 2
125000002572 propoxy group Chemical group [*]OC([H])([H])C(C([H])([H])[H])([H])[H] 0.000 claims description 2
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
229910052703 rhodium Inorganic materials 0.000 claims description 2
229910052707 ruthenium Inorganic materials 0.000 claims description 2
125000003375 sulfoxide group Chemical group 0.000 claims description 2
229910052717 sulfur Inorganic materials 0.000 claims description 2
125000004434 sulfur atom Chemical group 0.000 claims description 2
150000003568 thioethers Chemical class 0.000 claims description 2
125000002889 tridecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
125000002948 undecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
125000004429 atom Chemical group 0.000 claims 1
229910052751 metal Inorganic materials 0.000 claims 1
239000002184 metal Substances 0.000 claims 1
150000002739 metals Chemical class 0.000 claims 1
229920001021 polysulfide Polymers 0.000 claims 1
239000005077 polysulfide Substances 0.000 claims 1
230000007704 transition Effects 0.000 claims 1
239000000047 product Substances 0.000 description 14
238000006243 chemical reaction Methods 0.000 description 10
XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 9
239000003921 oil Substances 0.000 description 7
125000000524 functional group Chemical group 0.000 description 6
238000007306 functionalization reaction Methods 0.000 description 6
238000004519 manufacturing process Methods 0.000 description 6
KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 5
238000005481 NMR spectroscopy Methods 0.000 description 4
150000001336 alkenes Chemical class 0.000 description 4
PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 4
239000002243 precursor Substances 0.000 description 4
239000002904 solvent Substances 0.000 description 4
BBDKZWKEPDTENS-UHFFFAOYSA-N 4-Vinylcyclohexene Chemical group C=CC1CCC=CC1 BBDKZWKEPDTENS-UHFFFAOYSA-N 0.000 description 3
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
150000001298 alcohols Chemical class 0.000 description 3
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
229920001843 polymethylhydrosiloxane Polymers 0.000 description 3
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 description 2
238000006136 alcoholysis reaction Methods 0.000 description 2
230000008901 benefit Effects 0.000 description 2
238000006482 condensation reaction Methods 0.000 description 2
239000003431 cross linking reagent Substances 0.000 description 2
239000004205 dimethyl polysiloxane Substances 0.000 description 2
238000001704 evaporation Methods 0.000 description 2
150000002430 hydrocarbons Chemical group 0.000 description 2
229920000620 organic polymer Polymers 0.000 description 2
229920000435 poly(dimethylsiloxane) Polymers 0.000 description 2
229920000642 polymer Polymers 0.000 description 2
238000007789 sealing Methods 0.000 description 2
239000000126 substance Substances 0.000 description 2
238000006467 substitution reaction Methods 0.000 description 2
NWUYHJFMYQTDRP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;1-ethenyl-2-ethylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CCC1=CC=CC=C1C=C.C=CC1=CC=CC=C1C=C NWUYHJFMYQTDRP-UHFFFAOYSA-N 0.000 description 1
PRBHEGAFLDMLAL-UHFFFAOYSA-N 1,5-Hexadiene Natural products CC=CCC=C PRBHEGAFLDMLAL-UHFFFAOYSA-N 0.000 description 1
239000002841 Lewis acid Substances 0.000 description 1
240000005428 Pistacia lentiscus Species 0.000 description 1
239000002202 Polyethylene glycol Substances 0.000 description 1
239000007868 Raney catalyst Substances 0.000 description 1
229910000564 Raney nickel Inorganic materials 0.000 description 1
BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 1
239000002253 acid Substances 0.000 description 1
230000009471 action Effects 0.000 description 1
238000007259 addition reaction Methods 0.000 description 1
230000000181 anti-adherent effect Effects 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
239000013522 chelant Substances 0.000 description 1
239000003153 chemical reaction reagent Substances 0.000 description 1
238000000576 coating method Methods 0.000 description 1
239000000084 colloidal system Substances 0.000 description 1
239000012230 colorless oil Substances 0.000 description 1
238000004132 cross linking Methods 0.000 description 1
230000006866 deterioration Effects 0.000 description 1
AYOHIQLKSOJJQH-UHFFFAOYSA-N dibutyltin Chemical compound CCCC[Sn]CCCC AYOHIQLKSOJJQH-UHFFFAOYSA-N 0.000 description 1
239000012975 dibutyltin dilaurate Substances 0.000 description 1
NKSJNEHGWDZZQF-UHFFFAOYSA-N ethenyl(trimethoxy)silane Chemical compound CO[Si](OC)(OC)C=C NKSJNEHGWDZZQF-UHFFFAOYSA-N 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
239000012530 fluid Substances 0.000 description 1
229910021485 fumed silica Inorganic materials 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
AHAREKHAZNPPMI-UHFFFAOYSA-N hexa-1,3-diene Chemical compound CCC=CC=C AHAREKHAZNPPMI-UHFFFAOYSA-N 0.000 description 1
PYGSKMBEVAICCR-UHFFFAOYSA-N hexa-1,5-diene Chemical compound C=CCCC=C PYGSKMBEVAICCR-UHFFFAOYSA-N 0.000 description 1
230000007062 hydrolysis Effects 0.000 description 1
238000006460 hydrolysis reaction Methods 0.000 description 1
230000000977 initiatory effect Effects 0.000 description 1
239000013067 intermediate product Substances 0.000 description 1
238000011835 investigation Methods 0.000 description 1
239000003456 ion exchange resin Substances 0.000 description 1
229920003303 ion-exchange polymer Polymers 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
150000007517 lewis acids Chemical class 0.000 description 1
230000001050 lubricating effect Effects 0.000 description 1
229910001510 metal chloride Inorganic materials 0.000 description 1
239000002808 molecular sieve Substances 0.000 description 1
TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
239000012299 nitrogen atmosphere Substances 0.000 description 1
229910052760 oxygen Inorganic materials 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
125000004430 oxygen atom Chemical group O* 0.000 description 1
229920001223 polyethylene glycol Polymers 0.000 description 1
239000011253 protective coating Substances 0.000 description 1
239000002994 raw material Substances 0.000 description 1
230000003014 reinforcing effect Effects 0.000 description 1
230000035945 sensitivity Effects 0.000 description 1
229910000077 silane Inorganic materials 0.000 description 1
229920005573 silicon-containing polymer Polymers 0.000 description 1
URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 1
238000003756 stirring Methods 0.000 description 1
239000000758 substrate Substances 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
229910052723 transition metal Inorganic materials 0.000 description 1
150000003624 transition metals Chemical class 0.000 description 1
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
229920002554 vinyl polymer Polymers 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L83/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
- C08L83/04—Polysiloxanes
- C08L83/06—Polysiloxanes containing silicon bound to oxygen-containing groups
- 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
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/04—Polysiloxanes
- C08G77/38—Polysiloxanes modified by chemical after-treatment
- C08G77/382—Polysiloxanes modified by chemical after-treatment containing atoms other than carbon, hydrogen, oxygen or silicon
- C08G77/392—Polysiloxanes modified by chemical after-treatment containing atoms other than carbon, hydrogen, oxygen or silicon containing sulfur
- 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
- 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
- C07F7/21—Cyclic compounds having at least one ring containing silicon, but no carbon in 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
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/04—Polysiloxanes
- C08G77/38—Polysiloxanes modified by chemical after-treatment
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L83/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
- C08L83/04—Polysiloxanes
- C08L83/08—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
General Chemical & Material Sciences (AREA)
Silicon Polymers (AREA)
Compositions Of Macromolecular Compounds (AREA)
Paints Or Removers (AREA)
Dental Preparations (AREA)

NO972248A 1994-11-18 1997-05-16 Funksjonaliserte polyorganosiloksaner, fremgangsmÕte for fremstilling derav, og anvendelse derav NO309986B1 (no)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
FR9414056A FR2727118B1 (fr)	1994-11-18	1994-11-18	Polyorganosiloxanes fonctionnalises et l'un de leurs procedes de preparation
PCT/FR1995/001504 WO1996016125A1 (fr)	1994-11-18	1995-11-15	Polyorganosiloxanes fonctionnalises et l'un de leurs procedes de preparation

Publications (3)

Publication Number	Publication Date
NO972248D0 NO972248D0 (no)	1997-05-16
NO972248L NO972248L (no)	1997-07-18
NO309986B1 true NO309986B1 (no)	2001-04-30

Family

ID=9469088

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO972248A NO309986B1 (no)	1994-11-18	1997-05-16	Funksjonaliserte polyorganosiloksaner, fremgangsmÕte for fremstilling derav, og anvendelse derav

Country Status (23)

Country	Link
US (2)	US6140447A (de)
EP (1)	EP0792322B2 (de)
JP (1)	JP3086258B2 (de)
KR (1)	KR970707239A (de)
CN (1)	CN1083854C (de)
AR (1)	AR000486A1 (de)
AT (1)	ATE179739T1 (de)
AU (1)	AU709644B2 (de)
BR (1)	BR9510359A (de)
CA (1)	CA2204918C (de)
DE (1)	DE69509549T3 (de)
DK (1)	DK0792322T3 (de)
ES (1)	ES2132749T5 (de)
FR (1)	FR2727118B1 (de)
GR (1)	GR3030171T3 (de)
IL (1)	IL116024A0 (de)
MX (1)	MX9703561A (de)
NO (1)	NO309986B1 (de)
PL (1)	PL183214B1 (de)
TR (1)	TR199501441A2 (de)
TW (1)	TW383319B (de)
WO (1)	WO1996016125A1 (de)
ZA (1)	ZA959787B (de)

Families Citing this family (55)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
FR2727118B1 (fr) *	1994-11-18	1997-01-03	Rhone Poulenc Chimie	Polyorganosiloxanes fonctionnalises et l'un de leurs procedes de preparation
FR2742158B1 (fr)	1995-12-08	1998-01-02	Rhone Poulenc Chimie	Particules traitees par un polyorganosiloxane fonctionnalise leur procede de preparation et leur utilisation dans les polymeres thermoplastiques
FR2752239B1 (fr)	1996-08-06	1998-12-04	Rhone Poulenc Chimie	Procede de fabrication de polyorganosiloxanes (pos) multifonctionnels, par deshydrogenocondensation et hydrosilylation, et dispositif pour la mise en oeuvre de ce procede
US6472492B2 (en) *	1996-08-06	2002-10-29	Rhodia Chimie	Process for the manufacture of multifunctional polyorganosiloxanes (POSs) by dehydrocondensation and hydrosilylation, and device for carrying out this process
US6140450A (en) *	1996-12-27	2000-10-31	The Yokohama Rubber Co., Ltd.	Modified polysiloxanes, rubber compositions and tire tread rubber compositions containing the same, and reactive plasticizer
DE69804622T2 (de) *	1997-07-11	2002-09-12	Rhodia Chimie, Courbevoie	Verfahren zur herstellung von thiolgruppen-enthaltenden polyorganosiloxanen, mit diesem verfahren hergestellte organopolysiloxane und deren anwendung in gummi
US6140445A (en)	1998-04-17	2000-10-31	Crompton Corporation	Silane functional oligomer
US6602964B2 (en) *	1998-04-17	2003-08-05	Crompton Corporation	Reactive diluent in moisture curable system
DE19905820A1 (de) *	1998-10-27	2000-05-04	Degussa	Schwefelfunktionelle Polyorganosilane
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1995
- 1995-11-15 BR BR9510359A patent/BR9510359A/pt not_active Application Discontinuation
- 1995-11-15 CN CN95196294A patent/CN1083854C/zh not_active Expired - Fee Related
- 1995-11-15 AU AU41805/96A patent/AU709644B2/en not_active Ceased
- 1995-11-15 WO PCT/FR1995/001504 patent/WO1996016125A1/fr not_active Ceased
- 1995-11-15 TW TW084112062A patent/TW383319B/zh not_active IP Right Cessation
- 1995-11-15 AT AT95940317T patent/ATE179739T1/de not_active IP Right Cessation
- 1995-11-15 DK DK95940317T patent/DK0792322T3/da active
- 1995-11-15 JP JP08516617A patent/JP3086258B2/ja not_active Expired - Fee Related
- 1995-11-15 DE DE69509549T patent/DE69509549T3/de not_active Expired - Lifetime
- 1995-11-15 KR KR1019970703335A patent/KR970707239A/ko not_active Abandoned
- 1995-11-15 MX MX9703561A patent/MX9703561A/es not_active IP Right Cessation
- 1995-11-15 CA CA002204918A patent/CA2204918C/fr not_active Expired - Fee Related
- 1995-11-15 PL PL95320222A patent/PL183214B1/pl unknown
- 1995-11-15 EP EP95940317A patent/EP0792322B2/de not_active Expired - Lifetime
- 1995-11-15 ES ES95940317T patent/ES2132749T5/es not_active Expired - Lifetime
- 1995-11-16 IL IL11602495A patent/IL116024A0/xx unknown
- 1995-11-17 AR AR33427095A patent/AR000486A1/es unknown
- 1995-11-17 ZA ZA959787A patent/ZA959787B/xx unknown
- 1995-11-17 TR TR95/01441A patent/TR199501441A2/xx unknown
1997
- 1997-05-16 NO NO972248A patent/NO309986B1/no unknown
1999
- 1999-03-09 US US09/267,927 patent/US6140447A/en not_active Expired - Fee Related
- 1999-05-07 GR GR990401253T patent/GR3030171T3/el unknown
- 1999-12-03 US US09/454,879 patent/US6271331B1/en not_active Expired - Fee Related

Also Published As

Publication number	Publication date
DE69509549T2 (de)	1999-10-28
DK0792322T3 (da)	1999-11-01
US6271331B1 (en)	2001-08-07
JP3086258B2 (ja)	2000-09-11
WO1996016125A1 (fr)	1996-05-30
TR199501441A2 (tr)	1996-06-21
MX9703561A (es)	1997-08-30
KR970707239A (ko)	1997-12-01
ATE179739T1 (de)	1999-05-15
IL116024A0 (en)	1996-01-31
NO972248L (no)	1997-07-18
EP0792322B1 (de)	1999-05-06
TW383319B (en)	2000-03-01
AU709644B2 (en)	1999-09-02
ZA959787B (en)	1996-05-29
CN1165534A (zh)	1997-11-19
PL320222A1 (en)	1997-09-15
EP0792322A1 (de)	1997-09-03
DE69509549D1 (de)	1999-06-10
NO972248D0 (no)	1997-05-16
DE69509549T3 (de)	2004-06-09
AU4180596A (en)	1996-06-17
GR3030171T3 (en)	1999-08-31
EP0792322B2 (de)	2003-11-05
FR2727118B1 (fr)	1997-01-03
CA2204918A1 (fr)	1996-05-30
PL183214B1 (pl)	2002-06-28
ES2132749T3 (es)	1999-08-16
CA2204918C (fr)	2002-09-17
ES2132749T5 (es)	2004-05-01
CN1083854C (zh)	2002-05-01
US6140447A (en)	2000-10-31
AR000486A1 (es)	1997-07-10
FR2727118A1 (fr)	1996-05-24
JPH10501021A (ja)	1998-01-27
BR9510359A (pt)	1997-12-23

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