DE2646726C2 - Die Anlagerung verzögerndes Mittel bei der durch Platinkatalysator geförderten und bei Raumtemperatur erfolgenden Anlagerung von Si-gebundenem Wasserstoff an mindestens 50 Si-Atome je Molekul und aliphatische Mehrfachbindungen enthaltendes Organopolysiloxan - Google Patents
Die Anlagerung verzögerndes Mittel bei der durch Platinkatalysator geförderten und bei Raumtemperatur erfolgenden Anlagerung von Si-gebundenem Wasserstoff an mindestens 50 Si-Atome je Molekul und aliphatische Mehrfachbindungen enthaltendes OrganopolysiloxanInfo
- Publication number
- DE2646726C2 DE2646726C2 DE2646726A DE2646726A DE2646726C2 DE 2646726 C2 DE2646726 C2 DE 2646726C2 DE 2646726 A DE2646726 A DE 2646726A DE 2646726 A DE2646726 A DE 2646726A DE 2646726 C2 DE2646726 C2 DE 2646726C2
- Authority
- DE
- Germany
- Prior art keywords
- multiple bonds
- per molecule
- bonded hydrogen
- addition
- weight
- 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
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 title claims description 99
- 229910052697 platinum Inorganic materials 0.000 title claims description 49
- 229910052739 hydrogen Inorganic materials 0.000 title claims description 40
- 239000001257 hydrogen Substances 0.000 title claims description 40
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 title claims description 36
- 239000003054 catalyst Substances 0.000 title claims description 30
- 125000001931 aliphatic group Chemical group 0.000 title claims description 20
- 229920001296 polysiloxane Polymers 0.000 title claims description 20
- 239000003340 retarding agent Substances 0.000 title claims description 4
- 150000001875 compounds Chemical class 0.000 claims description 36
- -1 hydrocarbon radicals Chemical class 0.000 claims description 32
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 12
- 239000000126 substance Substances 0.000 claims description 12
- 239000004215 Carbon black (E152) Substances 0.000 claims description 8
- 229930195733 hydrocarbon Natural products 0.000 claims description 8
- 150000003254 radicals Chemical class 0.000 claims description 8
- 238000000034 method Methods 0.000 claims description 6
- 230000004048 modification Effects 0.000 claims description 6
- 238000012986 modification Methods 0.000 claims description 6
- 150000003961 organosilicon compounds Chemical class 0.000 claims description 5
- WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical compound [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 claims description 2
- 150000002894 organic compounds Chemical class 0.000 claims 1
- 239000000203 mixture Substances 0.000 description 43
- 238000002360 preparation method Methods 0.000 description 16
- 238000004132 cross linking Methods 0.000 description 13
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 11
- 229920001971 elastomer Polymers 0.000 description 11
- 239000000806 elastomer Substances 0.000 description 11
- 239000003085 diluting agent Substances 0.000 description 7
- 238000002474 experimental method Methods 0.000 description 7
- 239000000945 filler Substances 0.000 description 7
- 238000002156 mixing Methods 0.000 description 7
- 239000000047 product Substances 0.000 description 7
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 6
- 239000004205 dimethyl polysiloxane Substances 0.000 description 6
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 6
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 6
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 6
- LIVNPJMFVYWSIS-UHFFFAOYSA-N silicon monoxide Chemical compound [Si-]#[O+] LIVNPJMFVYWSIS-UHFFFAOYSA-N 0.000 description 6
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
- 229920001577 copolymer Polymers 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 5
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 4
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 4
- 235000013312 flour Nutrition 0.000 description 4
- 230000001698 pyrogenic effect Effects 0.000 description 4
- 239000000377 silicon dioxide Substances 0.000 description 4
- 235000012239 silicon dioxide Nutrition 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 125000004429 atom Chemical group 0.000 description 3
- 239000002978 dental impression material Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 230000002209 hydrophobic effect Effects 0.000 description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 239000000049 pigment Substances 0.000 description 3
- 238000000746 purification Methods 0.000 description 3
- 230000001105 regulatory effect Effects 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 2
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 239000012298 atmosphere Substances 0.000 description 2
- FSIJKGMIQTVTNP-UHFFFAOYSA-N bis(ethenyl)-methyl-trimethylsilyloxysilane Chemical compound C[Si](C)(C)O[Si](C)(C=C)C=C FSIJKGMIQTVTNP-UHFFFAOYSA-N 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 239000000706 filtrate Substances 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 150000002367 halogens Chemical class 0.000 description 2
- 150000002431 hydrogen Chemical class 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- XNLICIUVMPYHGG-UHFFFAOYSA-N pentan-2-one Chemical compound CCCC(C)=O XNLICIUVMPYHGG-UHFFFAOYSA-N 0.000 description 2
- 229910052698 phosphorus Inorganic materials 0.000 description 2
- 239000011574 phosphorus Substances 0.000 description 2
- 150000003057 platinum Chemical class 0.000 description 2
- NDBYXKQCPYUOMI-UHFFFAOYSA-N platinum(4+) Chemical compound [Pt+4] NDBYXKQCPYUOMI-UHFFFAOYSA-N 0.000 description 2
- 229920001843 polymethylhydrosiloxane Polymers 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 2
- KLFRPGNCEJNEKU-FDGPNNRMSA-L (z)-4-oxopent-2-en-2-olate;platinum(2+) Chemical compound [Pt+2].C\C([O-])=C\C(C)=O.C\C([O-])=C\C(C)=O KLFRPGNCEJNEKU-FDGPNNRMSA-L 0.000 description 1
- IHCCLXNEEPMSIO-UHFFFAOYSA-N 2-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperidin-1-yl]-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C1CCN(CC1)CC(=O)N1CC2=C(CC1)NN=N2 IHCCLXNEEPMSIO-UHFFFAOYSA-N 0.000 description 1
- 125000004182 2-chlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(*)C([H])=C1[H] 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- HNUALPPJLMYHDK-UHFFFAOYSA-N C[CH]C Chemical compound C[CH]C HNUALPPJLMYHDK-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- 241000625836 Ochrolechia Species 0.000 description 1
- 101710091688 Patatin Proteins 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 229910004283 SiO 4 Inorganic materials 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical group [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- 206010042618 Surgical procedure repeated Diseases 0.000 description 1
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 description 1
- YKTSYUJCYHOUJP-UHFFFAOYSA-N [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] Chemical compound [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] YKTSYUJCYHOUJP-UHFFFAOYSA-N 0.000 description 1
- FCCRGBVYSYHQRQ-UHFFFAOYSA-N [ethenyl(dimethyl)silyl]oxy-dimethylsilicon Chemical compound C[Si](C)O[Si](C)(C)C=C FCCRGBVYSYHQRQ-UHFFFAOYSA-N 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 235000019270 ammonium chloride Nutrition 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- UXJHQBVRZUANLK-UHFFFAOYSA-N azanylidyne(dichloro)-$l^{5}-phosphane Chemical compound ClP(Cl)#N UXJHQBVRZUANLK-UHFFFAOYSA-N 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 230000027455 binding Effects 0.000 description 1
- 238000009739 binding Methods 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 150000001721 carbon Chemical class 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- HXCKCCRKGXHOBK-UHFFFAOYSA-N cycloheptane Chemical compound [CH]1CCCCCC1 HXCKCCRKGXHOBK-UHFFFAOYSA-N 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical compound [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000000796 flavoring agent Substances 0.000 description 1
- 235000019634 flavors Nutrition 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 239000003517 fume Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 239000003446 ligand Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 125000005394 methallyl group Chemical group 0.000 description 1
- ACXIAEKDVUJRSK-UHFFFAOYSA-N methyl(silyloxy)silane Chemical compound C[SiH2]O[SiH3] ACXIAEKDVUJRSK-UHFFFAOYSA-N 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 230000006855 networking Effects 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 150000002897 organic nitrogen compounds Chemical class 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- UHZYTMXLRWXGPK-UHFFFAOYSA-N phosphorus pentachloride Chemical compound ClP(Cl)(Cl)(Cl)Cl UHZYTMXLRWXGPK-UHFFFAOYSA-N 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 239000002574 poison Substances 0.000 description 1
- 231100000614 poison Toxicity 0.000 description 1
- 239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 238000004382 potting Methods 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000002829 reductive effect Effects 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 239000005871 repellent Substances 0.000 description 1
- 230000000979 retarding effect Effects 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 229910052711 selenium Inorganic materials 0.000 description 1
- 239000011669 selenium Substances 0.000 description 1
- 238000007493 shaping process Methods 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 150000003464 sulfur compounds Chemical class 0.000 description 1
- 150000003527 tetrahydropyrans Chemical class 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- ORGHESHFQPYLAO-UHFFFAOYSA-N vinyl radical Chemical compound C=[CH] ORGHESHFQPYLAO-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 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
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/54—Silicon-containing compounds
-
- 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
- C08G77/12—Polysiloxanes containing silicon bound to hydrogen
-
- 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
- C08G77/20—Polysiloxanes containing silicon bound to unsaturated aliphatic groups
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Silicon Polymers (AREA)
- Paints Or Removers (AREA)
Priority Applications (12)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2646726A DE2646726C2 (de) | 1976-10-15 | 1976-10-15 | Die Anlagerung verzögerndes Mittel bei der durch Platinkatalysator geförderten und bei Raumtemperatur erfolgenden Anlagerung von Si-gebundenem Wasserstoff an mindestens 50 Si-Atome je Molekul und aliphatische Mehrfachbindungen enthaltendes Organopolysiloxan |
| NLAANVRAGE7708326,A NL184281C (nl) | 1976-10-15 | 1977-07-27 | Werkwijze voor het vertragen van de snelheid van de door platinakatalysator bevorderde additie van si-gebonden waterstof aan ten minste 50 siliciumatomen per molecuul en alifatische meervoudige bindingen bevattend organopolysiloxaan, alsmede gevormd voortbrengsel, vervaardigd met toepassing van een aldus bereid produkt. |
| GB37162/77A GB1570411A (en) | 1976-10-15 | 1977-09-06 | Manufacture of curable organopolysiloxane compositions |
| AU28843/77A AU512539B2 (en) | 1976-10-15 | 1977-09-15 | Manufacture of curable organopolysiloxane compositions |
| US05/838,414 US4096159A (en) | 1976-10-15 | 1977-09-30 | Process for controlling the rate of platinum induced addition reaction of silicon bonded hydrogen atoms to organopolysiloxanes containing aliphatic unsaturation |
| IT51397/77A IT1091310B (it) | 1976-10-15 | 1977-10-13 | Procedimento per addizionare ad organo-polisilossano idrogeno legato a si |
| AT0733077A AT378375B (de) | 1976-10-15 | 1977-10-13 | Verfahren zum regeln der geschwindigkeit der durch platinkatalysator gefoerderten anlagerung von si-gebundenem wasserstoff an organopolysiloxan |
| FR7730836A FR2367801A1 (fr) | 1976-10-15 | 1977-10-13 | Procede pour regler la vitesse d'addition, catalysee par |
| CA288,790A CA1099845A (en) | 1976-10-15 | 1977-10-14 | Process for controlling the rate of platinum induced addition reaction of silicon bonded hydrogen atoms to organopolysiloxanes containing alaphatic unsaturation |
| CH1261277A CH629513A5 (de) | 1976-10-15 | 1977-10-14 | Verfahren zum regeln der geschwindigkeit der durch platinkatalysator gefoerderten anlagerung von gruppen der formel (-)3si-h an aliphatische c,c-mehrfachbindungen enthaltendes organopolysiloxan. |
| BE181748A BE859735A (fr) | 1976-10-15 | 1977-10-14 | Procede pour regler la vitesse d'addition catalysee par le platine d'hydrogene lie au silicium sur un polyorganosiloxane a liaisons multiples aliphatiques |
| JP12339577A JPS5350263A (en) | 1976-10-15 | 1977-10-14 | Method of controlling addition velocity of sii bound hydrogen to organopolysiloxane having aliphatic multiibinding which if accelerated by platinum catalyst |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2646726A DE2646726C2 (de) | 1976-10-15 | 1976-10-15 | Die Anlagerung verzögerndes Mittel bei der durch Platinkatalysator geförderten und bei Raumtemperatur erfolgenden Anlagerung von Si-gebundenem Wasserstoff an mindestens 50 Si-Atome je Molekul und aliphatische Mehrfachbindungen enthaltendes Organopolysiloxan |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE2646726A1 DE2646726A1 (de) | 1978-04-20 |
| DE2646726C2 true DE2646726C2 (de) | 1988-07-28 |
Family
ID=5990596
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE2646726A Expired DE2646726C2 (de) | 1976-10-15 | 1976-10-15 | Die Anlagerung verzögerndes Mittel bei der durch Platinkatalysator geförderten und bei Raumtemperatur erfolgenden Anlagerung von Si-gebundenem Wasserstoff an mindestens 50 Si-Atome je Molekul und aliphatische Mehrfachbindungen enthaltendes Organopolysiloxan |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US4096159A (OSRAM) |
| JP (1) | JPS5350263A (OSRAM) |
| AT (1) | AT378375B (OSRAM) |
| AU (1) | AU512539B2 (OSRAM) |
| BE (1) | BE859735A (OSRAM) |
| CA (1) | CA1099845A (OSRAM) |
| CH (1) | CH629513A5 (OSRAM) |
| DE (1) | DE2646726C2 (OSRAM) |
| FR (1) | FR2367801A1 (OSRAM) |
| GB (1) | GB1570411A (OSRAM) |
| IT (1) | IT1091310B (OSRAM) |
| NL (1) | NL184281C (OSRAM) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1754740A2 (de) | 2005-08-20 | 2007-02-21 | Goldschmidt GmbH | Verfahren zur Herstellung von Anlagerungsprodukten aus SiH-Gruppen enthaltenden Verbindungen an eine Doppelbindung aufweisenden Reaktionspatner in wässrigen Medien |
| US8211972B2 (en) | 2008-09-26 | 2012-07-03 | Evonik Goldschmidt Gmbh | Emulsifier systems for cosmetic and pharmaceutical oil-in-water emulsions |
Families Citing this family (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4244912A (en) * | 1979-03-05 | 1981-01-13 | Dow Corning Corporation | Molding process using curable silicone release compositions |
| US4322320A (en) * | 1980-04-28 | 1982-03-30 | General Electric Company | Process for formulating silicone rubber products |
| NZ197154A (en) * | 1980-06-03 | 1984-02-03 | Gen Electric | Regulating the cure of silicone rubber compounds |
| ZA837448B (en) * | 1982-12-02 | 1984-05-30 | Gen Electric | Process for producing alkoxy-terminated polysiloxanes |
| DE3409139A1 (de) * | 1984-03-13 | 1985-09-19 | Wacker-Chemie GmbH, 8000 München | Platin, organopolysiloxan und fuellstoff enthaltende pasten |
| US5145886A (en) * | 1988-05-19 | 1992-09-08 | Minnesota Mining And Manufacturing Company | Radiation activated hydrosilation reaction |
| CA2014996A1 (en) * | 1989-05-19 | 1990-11-19 | Joel D. Oxman | Radiation activated hydrosilation reaction |
| DE4122310A1 (de) * | 1991-07-05 | 1993-01-07 | Bayer Ag | Transparentes material fuer dentale anwendungen |
| JP3454980B2 (ja) * | 1994-07-29 | 2003-10-06 | 株式会社ジーシー | 歯科印象用シリコーン組成物 |
| US5559183A (en) * | 1995-06-07 | 1996-09-24 | General Electric Company | Silicone oil-silica filler paste useful in liquid injection molding applications, method for making, and use |
| DE20221002U1 (de) * | 2002-12-12 | 2004-12-16 | Kettenbach Gmbh & Co. Kg | Additionsvernetzende Zweikomponenten-Siliconmaterialien mit hoher Shore D-Härte |
| EP1475069B1 (en) | 2003-05-09 | 2010-03-31 | 3M Espe AG | Curable silicone impression materials with high tear strength and low consistency |
| ATE316545T1 (de) | 2003-10-04 | 2006-02-15 | Goldschmidt Gmbh | Verfahren zur herstellung von organischen siliciumverbindungen |
| ES2543209T3 (es) | 2009-09-24 | 2015-08-17 | Evonik Degussa Gmbh | Polisiloxanos reticulados, proceso para su preparación y uso de los polisiloxanos reticulados en sistemas emulgentes para emulsiones de agua en aceite |
| DE102010029723A1 (de) | 2010-06-07 | 2011-12-08 | Evonik Goldschmidt Gmbh | Verfahren zur Herstellung von organischen Siliciumverbindungen |
| US9283153B2 (en) | 2011-08-12 | 2016-03-15 | 3M Innovative Properties Company | Curable composition with shortened setting time, process of production and use thereof |
| JP6043292B2 (ja) * | 2011-10-04 | 2016-12-14 | 株式会社カネカ | 硬化性樹脂組成物、硬化性樹脂組成物タブレット、成形体、半導体のパッケージ、半導体部品及び発光ダイオード |
| WO2014111503A2 (de) | 2013-01-18 | 2014-07-24 | Basf Se | Block-copolymere mit einem polydimethylsiloxan-block |
| DE102014213507A1 (de) | 2014-07-11 | 2016-01-14 | Evonik Degussa Gmbh | Platin enthaltende Zusammensetzung |
| EP3020749B1 (de) | 2014-11-12 | 2020-09-30 | Evonik Operations GmbH | Verfahren zur herstellung von platin enthaltenden zusammensetzungen |
| KR102592682B1 (ko) | 2015-11-09 | 2023-10-24 | 가부시키가이샤 시세이도 | 피부 위의 적용을 위한 조성물 및 방법 |
| EP3415547B1 (de) | 2017-06-13 | 2020-03-25 | Evonik Operations GmbH | Verfahren zur herstellung sic-verknüpfter polyethersiloxane |
| EP3415548B1 (de) | 2017-06-13 | 2020-03-25 | Evonik Operations GmbH | Verfahren zur herstellung sic-verknüpfter polyethersiloxane |
| JP2022528793A (ja) * | 2019-04-15 | 2022-06-15 | 株式会社 資生堂 | 皮膚に塗布する組成物及び方法 |
Family Cites Families (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2970150A (en) * | 1957-12-17 | 1961-01-31 | Union Carbide Corp | Processes for the reaction of silanic hydrogen-bonded siloxanes with unsaturated organic compounds with a platinum catalyst |
| DE1495964C3 (de) * | 1963-02-28 | 1974-10-17 | General Electric Co., Schenectady, N.Y. (V.St.A.) | Verfahren zur Stabilisierung einer copolymerisierbarenOrganopolysiloxanmischung |
| NL131800C (OSRAM) * | 1965-05-17 | |||
| US3344111A (en) * | 1966-09-28 | 1967-09-26 | Gen Electric | Preparation of stable copolymerizable organosilicon compositions containing a platinum catalyst and an acrylonitrile type compound |
| US3453233A (en) * | 1968-01-16 | 1969-07-01 | Dow Corning | Inhibited system for organosilicon compounds |
| JPS4810947B1 (OSRAM) * | 1969-08-15 | 1973-04-09 | ||
| BE755069A (fr) * | 1969-08-21 | 1971-02-22 | Dow Corning | Composition durcissable perfectionne a base de siloxanes |
| JPS4834382B1 (OSRAM) * | 1970-03-16 | 1973-10-20 | ||
| US3814730A (en) * | 1970-08-06 | 1974-06-04 | Gen Electric | Platinum complexes of unsaturated siloxanes and platinum containing organopolysiloxanes |
| US3923705A (en) * | 1974-10-30 | 1975-12-02 | Dow Corning | Method of preparing fire retardant siloxane foams and foams prepared therefrom |
| US3933882A (en) * | 1974-12-02 | 1976-01-20 | Dow Corning Corporation | Tube method for the preparation of olefinic siloxane compounds |
| US3971818A (en) * | 1974-12-02 | 1976-07-27 | Dow Corning Corporation | Method of preparing olefinic siloxane by GLC |
| US3933880A (en) * | 1974-12-02 | 1976-01-20 | Dow Corning Corporation | Method of preparing a platinum catalyst inhibitor |
| US4032502A (en) * | 1975-10-10 | 1977-06-28 | Dow Corning Corporation | Organosiloxane compositions for liquid injection |
-
1976
- 1976-10-15 DE DE2646726A patent/DE2646726C2/de not_active Expired
-
1977
- 1977-07-27 NL NLAANVRAGE7708326,A patent/NL184281C/xx not_active IP Right Cessation
- 1977-09-06 GB GB37162/77A patent/GB1570411A/en not_active Expired
- 1977-09-15 AU AU28843/77A patent/AU512539B2/en not_active Expired
- 1977-09-30 US US05/838,414 patent/US4096159A/en not_active Expired - Lifetime
- 1977-10-13 AT AT0733077A patent/AT378375B/de active
- 1977-10-13 FR FR7730836A patent/FR2367801A1/fr active Granted
- 1977-10-13 IT IT51397/77A patent/IT1091310B/it active
- 1977-10-14 CA CA288,790A patent/CA1099845A/en not_active Expired
- 1977-10-14 BE BE181748A patent/BE859735A/xx not_active IP Right Cessation
- 1977-10-14 JP JP12339577A patent/JPS5350263A/ja active Granted
- 1977-10-14 CH CH1261277A patent/CH629513A5/de not_active IP Right Cessation
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1754740A2 (de) | 2005-08-20 | 2007-02-21 | Goldschmidt GmbH | Verfahren zur Herstellung von Anlagerungsprodukten aus SiH-Gruppen enthaltenden Verbindungen an eine Doppelbindung aufweisenden Reaktionspatner in wässrigen Medien |
| US8211972B2 (en) | 2008-09-26 | 2012-07-03 | Evonik Goldschmidt Gmbh | Emulsifier systems for cosmetic and pharmaceutical oil-in-water emulsions |
Also Published As
| Publication number | Publication date |
|---|---|
| FR2367801A1 (fr) | 1978-05-12 |
| GB1570411A (en) | 1980-07-02 |
| BE859735A (fr) | 1978-04-14 |
| AT378375B (de) | 1985-07-25 |
| JPS5344505B2 (OSRAM) | 1978-11-29 |
| JPS5350263A (en) | 1978-05-08 |
| CA1099845A (en) | 1981-04-21 |
| NL184281C (nl) | 1989-06-01 |
| US4096159A (en) | 1978-06-20 |
| DE2646726A1 (de) | 1978-04-20 |
| FR2367801B1 (OSRAM) | 1979-05-11 |
| IT1091310B (it) | 1985-07-06 |
| CH629513A5 (de) | 1982-04-30 |
| NL7708326A (nl) | 1978-04-18 |
| ATA733077A (de) | 1984-12-15 |
| AU512539B2 (en) | 1980-10-16 |
| NL184281B (nl) | 1989-01-02 |
| AU2884377A (en) | 1979-03-22 |
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| 8363 | Opposition against the patent | ||
| 8366 | Restricted maintained after opposition proceedings | ||
| 8305 | Restricted maintenance of patent after opposition | ||
| D4 | Patent maintained restricted | ||
| 8339 | Ceased/non-payment of the annual fee |