CH443673A - Wärmehärtbare Mischung - Google Patents

Wärmehärtbare Mischung

Info

Publication number: CH443673A
Authority: CH; Switzerland
Prior art keywords: carbon atoms; radical; mixture according; units; parts
Prior art date: 1961-08-17

Application number

CH535462A

Other languages

German (de)

English (en)

Inventor

Earl Polmanteer Keith

Leroy Metevia Virgil

Original Assignee

Dow Corning

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.)

1961-08-17

Filing date

1962-05-04

Publication date

1967-09-15

1962-05-04 Application filed by Dow Corning filed Critical Dow Corning

1967-09-15 Publication of CH443673A publication Critical patent/CH443673A/de

Links

239000000203 mixture Substances 0.000 title claims description 27
229920001187 thermosetting polymer Polymers 0.000 title claims description 6
-1 siloxane units Chemical group 0.000 claims description 39
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical group O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 38
239000000945 filler Substances 0.000 claims description 34
125000004432 carbon atom Chemical group C* 0.000 claims description 21
229910052710 silicon Inorganic materials 0.000 claims description 21
229920000642 polymer Polymers 0.000 claims description 20
XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 16
239000010703 silicon Substances 0.000 claims description 15
239000000377 silicon dioxide Substances 0.000 claims description 15
125000001181 organosilyl group Chemical group [SiH3]* 0.000 claims description 13
125000004429 atom Chemical group 0.000 claims description 11
229910052760 oxygen Inorganic materials 0.000 claims description 11
239000001301 oxygen Substances 0.000 claims description 10
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 9
229910052681 coesite Inorganic materials 0.000 claims description 9
229910052906 cristobalite Inorganic materials 0.000 claims description 9
235000012239 silicon dioxide Nutrition 0.000 claims description 9
229910052682 stishovite Inorganic materials 0.000 claims description 9
229910052905 tridymite Inorganic materials 0.000 claims description 9
239000004215 Carbon black (E152) Substances 0.000 claims description 7
229930195733 hydrocarbon Natural products 0.000 claims description 7
238000004519 manufacturing process Methods 0.000 claims description 6
229920001558 organosilicon polymer Polymers 0.000 claims description 6
229920006395 saturated elastomer Polymers 0.000 claims description 6
229920002379 silicone rubber Polymers 0.000 claims description 6
239000004945 silicone rubber Substances 0.000 claims description 6
238000004073 vulcanization Methods 0.000 claims description 6
BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 claims description 5
CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 claims description 5
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 5
229910052605 nesosilicate Inorganic materials 0.000 claims description 4
150000004762 orthosilicates Chemical class 0.000 claims description 4
239000002245 particle Substances 0.000 claims description 4
150000004760 silicates Chemical class 0.000 claims description 4
125000004430 oxygen atom Chemical group O* 0.000 claims description 3
239000000470 constituent Substances 0.000 claims description 2
230000002209 hydrophobic effect Effects 0.000 claims description 2
238000010348 incorporation Methods 0.000 claims description 2
125000000962 organic group Chemical group 0.000 claims description 2
150000001451 organic peroxides Chemical class 0.000 claims description 2
239000007787 solid Substances 0.000 claims description 2
230000001419 dependent effect Effects 0.000 claims 1
239000004615 ingredient Substances 0.000 claims 1
125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 claims 1
229920001971 elastomer Polymers 0.000 description 27
239000000806 elastomer Substances 0.000 description 20
125000002887 hydroxy group Chemical group [H]O* 0.000 description 18
229920001577 copolymer Polymers 0.000 description 15
KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 10
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 9
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 9
239000000654 additive Substances 0.000 description 8
239000000463 material Substances 0.000 description 7
150000002978 peroxides Chemical class 0.000 description 7
239000005060 rubber Substances 0.000 description 7
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 5
230000000996 additive effect Effects 0.000 description 5
238000000034 method Methods 0.000 description 5
230000002787 reinforcement Effects 0.000 description 5
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 4
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 4
230000000704 physical effect Effects 0.000 description 4
239000000758 substrate Substances 0.000 description 4
GJBRNHKUVLOCEB-UHFFFAOYSA-N tert-butyl benzenecarboperoxoate Chemical compound CC(C)(C)OOC(=O)C1=CC=CC=C1 GJBRNHKUVLOCEB-UHFFFAOYSA-N 0.000 description 4
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
239000005046 Chlorosilane Substances 0.000 description 3
125000000217 alkyl group Chemical group 0.000 description 3
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
KOPOQZFJUQMUML-UHFFFAOYSA-N chlorosilane Chemical class Cl[SiH3] KOPOQZFJUQMUML-UHFFFAOYSA-N 0.000 description 3
150000001875 compounds Chemical class 0.000 description 3
239000000017 hydrogel Substances 0.000 description 3
NYMPGSQKHIOWIO-UHFFFAOYSA-N hydroxy(diphenyl)silicon Chemical class C=1C=CC=CC=1[Si](O)C1=CC=CC=C1 NYMPGSQKHIOWIO-UHFFFAOYSA-N 0.000 description 3
229920001296 polysiloxane Polymers 0.000 description 3
ZQZCOBSUOFHDEE-UHFFFAOYSA-N tetrapropyl silicate Chemical compound CCCO[Si](OCCC)(OCCC)OCCC ZQZCOBSUOFHDEE-UHFFFAOYSA-N 0.000 description 3
125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 3
WRXCBRHBHGNNQA-UHFFFAOYSA-N (2,4-dichlorobenzoyl) 2,4-dichlorobenzenecarboperoxoate Chemical compound ClC1=CC(Cl)=CC=C1C(=O)OOC(=O)C1=CC=C(Cl)C=C1Cl WRXCBRHBHGNNQA-UHFFFAOYSA-N 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 2
XMNIXWIUMCBBBL-UHFFFAOYSA-N 2-(2-phenylpropan-2-ylperoxy)propan-2-ylbenzene Chemical compound C=1C=CC=CC=1C(C)(C)OOC(C)(C)C1=CC=CC=C1 XMNIXWIUMCBBBL-UHFFFAOYSA-N 0.000 description 2
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 2
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical class OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 2
229920001400 block copolymer Polymers 0.000 description 2
238000009835 boiling Methods 0.000 description 2
238000006243 chemical reaction Methods 0.000 description 2
239000003795 chemical substances by application Substances 0.000 description 2
125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 2
239000004205 dimethyl polysiloxane Substances 0.000 description 2
235000013870 dimethyl polysiloxane Nutrition 0.000 description 2
239000000499 gel Substances 0.000 description 2
229920001519 homopolymer Polymers 0.000 description 2
239000003456 ion exchange resin Substances 0.000 description 2
229920003303 ion-exchange polymer Polymers 0.000 description 2
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
239000007788 liquid Substances 0.000 description 2
150000003961 organosilicon compounds Chemical class 0.000 description 2
125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 2
229920000435 poly(dimethylsiloxane) Polymers 0.000 description 2
239000011347 resin Substances 0.000 description 2
229920005989 resin Polymers 0.000 description 2
238000009738 saturating Methods 0.000 description 2
239000000741 silica gel Substances 0.000 description 2
229910002027 silica gel Inorganic materials 0.000 description 2
RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 2
YHLJHYMNIZNTGJ-UHFFFAOYSA-N trihydroxy(pentoxy)silane Chemical compound CCCCCO[Si](O)(O)O YHLJHYMNIZNTGJ-UHFFFAOYSA-N 0.000 description 2
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
229920002554 vinyl polymer Polymers 0.000 description 2
125000000349 (Z)-3-carboxyprop-2-enoyl group Chemical group O=C([*])/C([H])=C([H])\C(O[H])=O 0.000 description 1
SJCXNCOPILPTCJ-UHFFFAOYSA-N 2-oxatricyclo[7.2.2.23,6]pentadeca-1(11),3(15),4,6(14),9,12-hexaene Chemical compound O1C(C=C2)=CC=C2CCC2=CC=C1C=C2 SJCXNCOPILPTCJ-UHFFFAOYSA-N 0.000 description 1
239000004342 Benzoyl peroxide Substances 0.000 description 1
OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
239000005909 Kieselgur Substances 0.000 description 1
241000625836 Ochrolechia Species 0.000 description 1
241000158147 Sator Species 0.000 description 1
229910020175 SiOH Inorganic materials 0.000 description 1
BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
239000004115 Sodium Silicate Substances 0.000 description 1
BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 description 1
241000607479 Yersinia pestis Species 0.000 description 1
238000010521 absorption reaction Methods 0.000 description 1
230000002378 acidificating effect Effects 0.000 description 1
238000005054 agglomeration Methods 0.000 description 1
230000002776 aggregation Effects 0.000 description 1
229910052910 alkali metal silicate Inorganic materials 0.000 description 1
125000003342 alkenyl group Chemical group 0.000 description 1
125000002877 alkyl aryl group Chemical group 0.000 description 1
239000003963 antioxidant agent Substances 0.000 description 1
125000003710 aryl alkyl group Chemical group 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
235000019400 benzoyl peroxide Nutrition 0.000 description 1
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
125000004799 bromophenyl group Chemical group 0.000 description 1
229940043430 calcium compound Drugs 0.000 description 1
150000001674 calcium compounds Chemical class 0.000 description 1
239000003054 catalyst Substances 0.000 description 1
230000003197 catalytic effect Effects 0.000 description 1
239000000460 chlorine Substances 0.000 description 1
229910052801 chlorine Inorganic materials 0.000 description 1
125000004218 chloromethyl group Chemical group [H]C([H])(Cl)* 0.000 description 1
230000000052 comparative effect Effects 0.000 description 1
125000000392 cycloalkenyl group Chemical group 0.000 description 1
125000000753 cycloalkyl group Chemical group 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
238000000354 decomposition reaction Methods 0.000 description 1
LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical compound CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 description 1
QGBSISYHAICWAH-UHFFFAOYSA-N dicyandiamide Chemical compound NC(N)=NC#N QGBSISYHAICWAH-UHFFFAOYSA-N 0.000 description 1
WXAYXYTUOFVMKE-UHFFFAOYSA-N diethyl dipropyl silicate Chemical compound CCCO[Si](OCC)(OCC)OCCC WXAYXYTUOFVMKE-UHFFFAOYSA-N 0.000 description 1
230000008030 elimination Effects 0.000 description 1
238000003379 elimination reaction Methods 0.000 description 1
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
238000006266 etherification reaction Methods 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
239000006260 foam Substances 0.000 description 1
239000012760 heat stabilizer Substances 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
VLKZOEOYAKHREP-UHFFFAOYSA-N hexane Substances CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 1
LDQZFVDUJRXKNP-UHFFFAOYSA-N hexoxy(trihydroxy)silane Chemical compound CCCCCCO[Si](O)(O)O LDQZFVDUJRXKNP-UHFFFAOYSA-N 0.000 description 1
230000007062 hydrolysis Effects 0.000 description 1
238000006460 hydrolysis reaction Methods 0.000 description 1
PQPVPZTVJLXQAS-UHFFFAOYSA-N hydroxy-methyl-phenylsilicon Chemical class C[Si](O)C1=CC=CC=C1 PQPVPZTVJLXQAS-UHFFFAOYSA-N 0.000 description 1
230000005764 inhibitory process Effects 0.000 description 1
238000005304 joining Methods 0.000 description 1
125000005394 methallyl group Chemical group 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
230000007935 neutral effect Effects 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
239000003921 oil Substances 0.000 description 1
239000012766 organic filler Substances 0.000 description 1
239000012074 organic phase Substances 0.000 description 1
125000005375 organosiloxane group Chemical group 0.000 description 1
NRNFFDZCBYOZJY-UHFFFAOYSA-N p-quinodimethane Chemical group C=C1C=CC(=C)C=C1 NRNFFDZCBYOZJY-UHFFFAOYSA-N 0.000 description 1
238000010422 painting Methods 0.000 description 1
238000010060 peroxide vulcanization Methods 0.000 description 1
239000000049 pigment Substances 0.000 description 1
239000004014 plasticizer Substances 0.000 description 1
238000011417 postcuring Methods 0.000 description 1
230000002028 premature Effects 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000002994 raw material Substances 0.000 description 1
229910000077 silane Inorganic materials 0.000 description 1
150000004819 silanols Chemical class 0.000 description 1
NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
229910052911 sodium silicate Inorganic materials 0.000 description 1
239000002904 solvent Substances 0.000 description 1
239000007858 starting material Substances 0.000 description 1
125000004079 stearyl 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])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
238000003756 stirring Methods 0.000 description 1
239000000126 substance Substances 0.000 description 1
238000006467 substitution reaction Methods 0.000 description 1
235000012976 tarts Nutrition 0.000 description 1
LYDRKKWPKKEMNZ-UHFFFAOYSA-N tert-butyl benzoate Chemical compound CC(C)(C)OC(=O)C1=CC=CC=C1 LYDRKKWPKKEMNZ-UHFFFAOYSA-N 0.000 description 1
LFQCEHFDDXELDD-UHFFFAOYSA-N tetramethyl orthosilicate Chemical compound CO[Si](OC)(OC)OC LFQCEHFDDXELDD-UHFFFAOYSA-N 0.000 description 1
125000003944 tolyl group Chemical group 0.000 description 1
ZEOPCIFVJGABLT-UHFFFAOYSA-N trihydroxy(2-methoxyethoxy)silane Chemical compound COCCO[Si](O)(O)O ZEOPCIFVJGABLT-UHFFFAOYSA-N 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
125000005023 xylyl group Chemical group 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
- C08K5/16—Nitrogen-containing compounds
- C08K5/315—Compounds containing carbon-to-nitrogen triple bonds
- 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
- C08G77/14—Polysiloxanes containing silicon bound to oxygen-containing groups
- C08G77/16—Polysiloxanes containing silicon bound to oxygen-containing groups to hydroxyl 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
- C08G77/22—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen
- C08G77/24—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen halogen-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
- C08G77/60—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 in which all the silicon atoms are connected by linkages other than oxygen atoms

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)
Silicon Polymers (AREA)

CH535462A 1961-08-17 1962-05-04 Wärmehärtbare Mischung CH443673A (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US13198761A	1961-08-17	1961-08-17

Publications (1)

Publication Number	Publication Date
CH443673A true CH443673A (de)	1967-09-15

Family

ID=22451903

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CH535462A CH443673A (de)	1961-08-17	1962-05-04	Wärmehärtbare Mischung

Country Status (5)

Country	Link
BE (1)	BE621432A (fr)
CH (1)	CH443673A (fr)
DE (1)	DE1166470B (fr)
GB (1)	GB959525A (fr)
NL (1)	NL278036A (fr)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3308203A (en) *	1964-06-24	1967-03-07	Dow Corning	Polysiloxane block copolymer rubber and process for making same
CA2055303A1 (fr) *	1990-12-03	1992-06-04	Michael K. J. Lee	Compositions de copolymeres statistiques durcissables de dimethylsiloxane/diphenylsiloxane

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
FR1093400A (fr) *		1955-05-03

0
- NL NL278036D patent/NL278036A/xx unknown
1962
- 1962-05-04 CH CH535462A patent/CH443673A/de unknown
- 1962-08-03 GB GB2995462A patent/GB959525A/en not_active Expired
- 1962-08-16 BE BE621432A patent/BE621432A/fr unknown
- 1962-08-17 DE DED39640A patent/DE1166470B/de active Pending

Also Published As

Publication number	Publication date
GB959525A (en)	1964-06-03
NL278036A (fr)
DE1166470B (de)	1964-03-26
BE621432A (fr)	1963-02-18

Publication	Publication Date	Title
DE69129053T2 (de)	1998-10-15	Warmhärtbare Siliconelastomerzusammensetzungen
DE69331359T2 (de)	2002-08-22	Polysiloxankautschukzusammensetzungen
DE2358784A1 (de)	1974-06-06	Kalt haertende silikon-kautschukzusammensetzungen
DE2238914B2 (de)	1974-01-03	Hitzehärtbare Organopolysiloxanformmassen
CH497486A (de)	1970-10-15	Verfahren zur Herstellung eines Siloxanpolymers
DE2054286C3 (de)	1979-01-04	Verfahren zur Herstellung von siliciumorganischen Füll- und Verstärkungsstoffen für Polymere
DE2020114B2 (de)	1977-11-10	Vulkanisierbare, vinylgruppen enthaltende organopolysiloxanformmasse
DE2535334A1 (de)	1977-02-17	Verfahren zur homogenen verteilung hochdisperser aktiver fuellstoffe in polyorganosiloxanen
DE2350369A1 (de)	1974-04-25	Verfahren zur herstellung von diorganopolysiloxanen
DE1224040B (de)	1966-09-01	Bei Raumtemperatur durchfuehrbares Verfahren zur Herstellung von elastomeren Zell-, Schwamm- oder Schaumkoerpern aus linearen Organopolysiloxanen
DE10319303A1 (de)	2004-12-09	Verfahren zur Herstellung von vernetzbaren Massen auf der Basis von Organosiliciumverbindungen
CH529809A (de)	1972-12-31	Verfahren zur Herstellung eines Siloxanblockcopolymerisats und dessen Verwendung
DE1902086B2 (de)	1970-10-15	Stabilisierung der Lagerfähigkeit hitzehärtbarer Formmassen auf Grundlage von Qrganosiliciumverbindungen
DE2900707A1 (de)	1979-07-19	Hitzehaertbare silikonkautschukmassen
DE3213053A1 (de)	1982-11-11	Fluorsilicon-kautschukmasse, verfahren zu ihrer haertung und polymer
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