CA2064386A1 - Organosilicon compositions containing siloxane elastomers - Google Patents
Organosilicon compositions containing siloxane elastomersInfo
- Publication number
- CA2064386A1 CA2064386A1 CA002064386A CA2064386A CA2064386A1 CA 2064386 A1 CA2064386 A1 CA 2064386A1 CA 002064386 A CA002064386 A CA 002064386A CA 2064386 A CA2064386 A CA 2064386A CA 2064386 A1 CA2064386 A1 CA 2064386A1
- Authority
- CA
- Canada
- Prior art keywords
- composition
- carbon
- elastomer
- polycyclic
- polymer
- 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.)
- Abandoned
Links
- 229920001971 elastomer Polymers 0.000 title claims abstract description 31
- 239000000806 elastomer Substances 0.000 title claims abstract description 31
- 239000000203 mixture Substances 0.000 title claims abstract description 29
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 title claims abstract description 12
- -1 polysiloxane Polymers 0.000 claims abstract description 59
- 229920000642 polymer Polymers 0.000 claims abstract description 32
- 239000011203 carbon fibre reinforced carbon Substances 0.000 claims abstract description 26
- 125000003118 aryl group Chemical group 0.000 claims abstract description 17
- 125000004122 cyclic group Chemical group 0.000 claims abstract description 17
- 238000006459 hydrosilylation reaction Methods 0.000 claims abstract description 14
- 229920001296 polysiloxane Polymers 0.000 claims abstract description 13
- 150000002430 hydrocarbons Chemical group 0.000 claims abstract description 8
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 6
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 5
- 229920001558 organosilicon polymer Polymers 0.000 claims abstract description 5
- 229910052710 silicon Inorganic materials 0.000 claims abstract 2
- 239000010703 silicon Substances 0.000 claims abstract 2
- ZSWFCLXCOIISFI-UHFFFAOYSA-N cyclopentadiene Chemical compound C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 claims description 10
- 239000002245 particle Substances 0.000 claims description 6
- HECLRDQVFMWTQS-RGOKHQFPSA-N 1755-01-7 Chemical compound C1[C@H]2[C@@H]3CC=C[C@@H]3[C@@H]1C=C2 HECLRDQVFMWTQS-RGOKHQFPSA-N 0.000 claims description 5
- 125000000217 alkyl group Chemical group 0.000 claims description 5
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 claims description 5
- 229920002554 vinyl polymer Polymers 0.000 claims description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 3
- KAJRUHJCBCZULP-UHFFFAOYSA-N 1-cyclohepta-1,3-dien-1-ylcyclohepta-1,3-diene Chemical compound C1CCC=CC=C1C1=CC=CCCC1 KAJRUHJCBCZULP-UHFFFAOYSA-N 0.000 claims description 2
- 125000003342 alkenyl group Chemical group 0.000 claims description 2
- SJYNFBVQFBRSIB-UHFFFAOYSA-N norbornadiene Chemical compound C1=CC2C=CC1C2 SJYNFBVQFBRSIB-UHFFFAOYSA-N 0.000 claims description 2
- 150000002846 norbornadienes Chemical class 0.000 claims description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 2
- 238000005698 Diels-Alder reaction Methods 0.000 claims 1
- NYMPGSQKHIOWIO-UHFFFAOYSA-N hydroxy(diphenyl)silicon Chemical compound C=1C=CC=CC=1[Si](O)C1=CC=CC=C1 NYMPGSQKHIOWIO-UHFFFAOYSA-N 0.000 claims 1
- KAKZBPTYRLMSJV-UHFFFAOYSA-N vinyl-ethylene Natural products C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims 1
- 238000006243 chemical reaction Methods 0.000 description 15
- 239000003054 catalyst Substances 0.000 description 8
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 8
- 235000010290 biphenyl Nutrition 0.000 description 7
- 239000004305 biphenyl Substances 0.000 description 7
- 229920001577 copolymer Polymers 0.000 description 7
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 7
- 239000007788 liquid Substances 0.000 description 6
- 239000004215 Carbon black (E152) Substances 0.000 description 5
- 125000006267 biphenyl group Chemical group 0.000 description 5
- 229930195733 hydrocarbon Natural products 0.000 description 5
- 125000000962 organic group Chemical group 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- HECLRDQVFMWTQS-UHFFFAOYSA-N Dicyclopentadiene Chemical compound C1C2C3CC=CC3C1C=C2 HECLRDQVFMWTQS-UHFFFAOYSA-N 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 239000000945 filler Substances 0.000 description 4
- 229910052739 hydrogen Inorganic materials 0.000 description 4
- 239000001257 hydrogen Substances 0.000 description 4
- 150000002500 ions Chemical class 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 229910052697 platinum Inorganic materials 0.000 description 4
- 125000003367 polycyclic group Chemical group 0.000 description 4
- 239000000376 reactant Substances 0.000 description 4
- 238000003860 storage Methods 0.000 description 4
- 229920001187 thermosetting polymer Polymers 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000000853 adhesive Substances 0.000 description 3
- 230000001070 adhesive effect Effects 0.000 description 3
- 230000009969 flowable effect Effects 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-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
- 229910018557 Si O Inorganic materials 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 150000001336 alkenes Chemical class 0.000 description 2
- 238000013459 approach Methods 0.000 description 2
- 125000004429 atom Chemical group 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 239000002131 composite material Substances 0.000 description 2
- 125000001047 cyclobutenyl group Chemical group C1(=CCC1)* 0.000 description 2
- 229910003460 diamond Inorganic materials 0.000 description 2
- 239000010432 diamond Substances 0.000 description 2
- 239000008393 encapsulating agent Substances 0.000 description 2
- ZZUFCTLCJUWOSV-UHFFFAOYSA-N furosemide Chemical compound C1=C(Cl)C(S(=O)(=O)N)=CC(C(O)=O)=C1NCC1=CC=CO1 ZZUFCTLCJUWOSV-UHFFFAOYSA-N 0.000 description 2
- 239000000499 gel Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 2
- 150000004291 polyenes Chemical class 0.000 description 2
- 238000004382 potting Methods 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- LIVNPJMFVYWSIS-UHFFFAOYSA-N silicon monoxide Inorganic materials [Si-]#[O+] LIVNPJMFVYWSIS-UHFFFAOYSA-N 0.000 description 2
- 125000004469 siloxy group Chemical group [SiH3]O* 0.000 description 2
- 230000007704 transition Effects 0.000 description 2
- FOHNTMRACRPKES-UHFFFAOYSA-N 2,2,4,4,6,6,8-heptamethyl-1,3,5,7,9,2,4,6,8,10-pentaoxapentasilecane Chemical compound C[SiH]1O[SiH2]O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O1 FOHNTMRACRPKES-UHFFFAOYSA-N 0.000 description 1
- PUNGSQUVTIDKNU-UHFFFAOYSA-N 2,4,6,8,10-pentamethyl-1,3,5,7,9,2$l^{3},4$l^{3},6$l^{3},8$l^{3},10$l^{3}-pentaoxapentasilecane Chemical compound C[Si]1O[Si](C)O[Si](C)O[Si](C)O[Si](C)O1 PUNGSQUVTIDKNU-UHFFFAOYSA-N 0.000 description 1
- ATVJXMYDOSMEPO-UHFFFAOYSA-N 3-prop-2-enoxyprop-1-ene Chemical compound C=CCOCC=C ATVJXMYDOSMEPO-UHFFFAOYSA-N 0.000 description 1
- INYHZQLKOKTDAI-UHFFFAOYSA-N 5-ethenylbicyclo[2.2.1]hept-2-ene Chemical compound C1C2C(C=C)CC1C=C2 INYHZQLKOKTDAI-UHFFFAOYSA-N 0.000 description 1
- UTBCLIMIBBSDLG-UHFFFAOYSA-N C12=CC=CCC2C2CC2C2C1C2 Chemical compound C12=CC=CCC2C2CC2C2C1C2 UTBCLIMIBBSDLG-UHFFFAOYSA-N 0.000 description 1
- BPMGYFSWCJZSBA-UHFFFAOYSA-N C[SiH](C)O[SiH3] Chemical compound C[SiH](C)O[SiH3] BPMGYFSWCJZSBA-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 101100536354 Drosophila melanogaster tant gene Proteins 0.000 description 1
- 239000004606 Fillers/Extenders Substances 0.000 description 1
- 101100536883 Legionella pneumophila subsp. pneumophila (strain Philadelphia 1 / ATCC 33152 / DSM 7513) thi5 gene Proteins 0.000 description 1
- 241001274660 Modulus Species 0.000 description 1
- KWYHDKDOAIKMQN-UHFFFAOYSA-N N,N,N',N'-tetramethylethylenediamine Chemical compound CN(C)CCN(C)C KWYHDKDOAIKMQN-UHFFFAOYSA-N 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
- 229910019032 PtCl2 Inorganic materials 0.000 description 1
- 101100240664 Schizosaccharomyces pombe (strain 972 / ATCC 24843) nmt1 gene Proteins 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 241000193803 Therea Species 0.000 description 1
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical class [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- FLPKSBDJMLUTEX-UHFFFAOYSA-N bis(1,2,2,6,6-pentamethylpiperidin-4-yl) 2-butyl-2-[(3,5-ditert-butyl-4-hydroxyphenyl)methyl]propanedioate Chemical compound C1C(C)(C)N(C)C(C)(C)CC1OC(=O)C(C(=O)OC1CC(C)(C)N(C)C(C)(C)C1)(CCCC)CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 FLPKSBDJMLUTEX-UHFFFAOYSA-N 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- QXJJQWWVWRCVQT-UHFFFAOYSA-K calcium;sodium;phosphate Chemical compound [Na+].[Ca+2].[O-]P([O-])([O-])=O QXJJQWWVWRCVQT-UHFFFAOYSA-K 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- CREMABGTGYGIQB-UHFFFAOYSA-N carbon carbon Chemical compound C.C CREMABGTGYGIQB-UHFFFAOYSA-N 0.000 description 1
- 239000004568 cement Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 239000008139 complexing agent Substances 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 230000002844 continuous effect Effects 0.000 description 1
- 239000011889 copper foil Substances 0.000 description 1
- 229920006037 cross link polymer Polymers 0.000 description 1
- CFBGXYDUODCMNS-UHFFFAOYSA-N cyclobutene Chemical compound C1CC=C1 CFBGXYDUODCMNS-UHFFFAOYSA-N 0.000 description 1
- DDJSWKLBKSLAAZ-UHFFFAOYSA-N cyclotetrasiloxane Chemical compound O1[SiH2]O[SiH2]O[SiH2]O[SiH2]1 DDJSWKLBKSLAAZ-UHFFFAOYSA-N 0.000 description 1
- 125000005675 difluoroethenyl group Chemical group [H]C(*)=C(F)F 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000001493 electron microscopy Methods 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 229910021485 fumed silica Inorganic materials 0.000 description 1
- 239000005350 fused silica glass Substances 0.000 description 1
- 239000005337 ground glass Substances 0.000 description 1
- 229910021472 group 8 element Inorganic materials 0.000 description 1
- UCQHUEOREKHIBP-UHFFFAOYSA-N heptacyclo[9.6.1.14,7.113,16.02,10.03,8.012,17]icosa-5,14-diene Chemical compound C1C(C23)C4C(C=C5)CC5C4C1C3CC1C2C2C=CC1C2 UCQHUEOREKHIBP-UHFFFAOYSA-N 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 125000004464 hydroxyphenyl group Chemical group 0.000 description 1
- 230000003116 impacting effect Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- JFNLZVQOOSMTJK-KNVOCYPGSA-N norbornene Chemical compound C1[C@@H]2CC[C@H]1C=C2 JFNLZVQOOSMTJK-KNVOCYPGSA-N 0.000 description 1
- SSDSCDGVMJFTEQ-UHFFFAOYSA-N octadecyl 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CCC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 SSDSCDGVMJFTEQ-UHFFFAOYSA-N 0.000 description 1
- 230000009965 odorless effect Effects 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 150000003018 phosphorus compounds Chemical class 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920005567 polycyclic polymer Polymers 0.000 description 1
- 230000001902 propagating effect Effects 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000010926 purge Methods 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 230000036632 reaction speed Effects 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 238000003303 reheating Methods 0.000 description 1
- 230000002787 reinforcement Effects 0.000 description 1
- IOVGROKTTNBUGK-SJCJKPOMSA-N ritodrine Chemical compound N([C@@H](C)[C@H](O)C=1C=CC(O)=CC=1)CCC1=CC=C(O)C=C1 IOVGROKTTNBUGK-SJCJKPOMSA-N 0.000 description 1
- 238000010079 rubber tapping Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 101150016746 sigI gene Proteins 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000003381 stabilizer 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
- 125000000547 substituted alkyl group Chemical group 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 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 description 1
- 239000010455 vermiculite Substances 0.000 description 1
- 229910052902 vermiculite Inorganic materials 0.000 description 1
- 235000019354 vermiculite Nutrition 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 239000010456 wollastonite Substances 0.000 description 1
- 229910052882 wollastonite Inorganic materials 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
- 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
- C08G77/42—Block-or graft-polymers containing polysiloxane sequences
- C08G77/44—Block-or graft-polymers containing polysiloxane sequences containing only polysiloxane sequences
-
- 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
- C08L83/14—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 in which at least two but not 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)
- Silicon Polymers (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US685,360 | 1991-04-15 | ||
| US07/685,360 US5171817A (en) | 1991-04-15 | 1991-04-15 | Organosilicon compositions containing siloxane elastomers |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2064386A1 true CA2064386A1 (en) | 1992-10-16 |
Family
ID=24751862
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002064386A Abandoned CA2064386A1 (en) | 1991-04-15 | 1992-03-31 | Organosilicon compositions containing siloxane elastomers |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US5171817A (enExample) |
| EP (1) | EP0509373B1 (enExample) |
| JP (1) | JP3288423B2 (enExample) |
| KR (1) | KR100192721B1 (enExample) |
| CA (1) | CA2064386A1 (enExample) |
| DE (1) | DE69215950T2 (enExample) |
| TW (1) | TW208036B (enExample) |
Families Citing this family (31)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5298536A (en) * | 1992-02-21 | 1994-03-29 | Hercules Incorporated | Flame retardant organosilicon polymer composition, process for making same, and article produced therefrom |
| US5523374A (en) * | 1992-12-03 | 1996-06-04 | Hercules Incorporated | Curable and cured organosilicon compositions |
| US5391678A (en) * | 1992-12-03 | 1995-02-21 | Hercules Incorporated | Curable and cured organosilicon compositions |
| US5408026A (en) * | 1993-08-23 | 1995-04-18 | Cowan; Patrick J. | Curable and cured organosilicon compositions, and process for making same |
| US5451637A (en) * | 1994-05-10 | 1995-09-19 | Hercules Incorporated | Organosilicon compositions prepared from unsaturated elastomeric polymers |
| US5512376A (en) * | 1994-06-20 | 1996-04-30 | Hercules Incorporated | Nonpolar polymers comprising antiplasticizers |
| US5859105A (en) * | 1997-02-11 | 1999-01-12 | Johnson Matthey, Inc. | Organosilicon-containing compositions capable of rapid curing at low temperature |
| US5852092A (en) * | 1997-02-11 | 1998-12-22 | Johnson Matthey, Inc. | Organosilicon-containing compositions having enhanced adhesive properties |
| JP4921657B2 (ja) * | 2001-09-05 | 2012-04-25 | 株式会社カネカ | 光学材料用硬化性組成物、光学用材料、その製造方法およびそれを用いた発光ダイオード |
| JP2003073551A (ja) * | 2001-09-06 | 2003-03-12 | Kanegafuchi Chem Ind Co Ltd | 硬化性組成物、硬化物及びその製造方法 |
| US6841647B2 (en) * | 2001-11-06 | 2005-01-11 | National Starch And Chemical Investment Holding Corporation | Fluid resistant silicone encapsulant |
| CN100354372C (zh) * | 2002-05-01 | 2007-12-12 | 陶氏康宁公司 | 槽池寿命改进的组合物 |
| US6822066B2 (en) | 2002-11-18 | 2004-11-23 | Dow Corning Corporation | Organosiloxane resin-polyene materials |
| DE102004039111A1 (de) * | 2003-08-14 | 2005-04-14 | Shin-Etsu Chemical Co., Ltd. | Härtbare Silikonharzzusammensetzung |
| TW200513483A (en) * | 2003-10-10 | 2005-04-16 | Shinetsu Chemical Co | Curable composition |
| US7452577B2 (en) | 2004-06-30 | 2008-11-18 | Freudenberg-Nok General Partnership | Electron beam curing of fabricated polymeric structures |
| US20060000801A1 (en) | 2004-06-30 | 2006-01-05 | Park Edward H | Surface bonding in halogenated polymeric components |
| US7521508B2 (en) * | 2004-06-30 | 2009-04-21 | Freudenberg-Nok General Partnership | Electron beam inter-curing of plastic and elastomer blends |
| US7230038B2 (en) | 2004-06-30 | 2007-06-12 | Freudenberg-Nok General Partnership | Branched chain fluoropolymers |
| US7342072B2 (en) | 2004-06-30 | 2008-03-11 | Freudenberg-Nok General Partnership | Bimodal compounds having an elastomeric moiety |
| US7135535B2 (en) * | 2004-07-29 | 2006-11-14 | National Starch And Chemical Investment Holding Corporation | Siloxane resins with oxetane functionality |
| US7381765B2 (en) | 2004-11-08 | 2008-06-03 | Freudenberg-Nok General Partnership | Electrostatically dissipative fluoropolymers |
| JP2007077252A (ja) * | 2005-09-13 | 2007-03-29 | Shin Etsu Chem Co Ltd | 硬化性シリコーン組成物 |
| KR101387209B1 (ko) * | 2006-03-21 | 2014-04-21 | 다우 코닝 코포레이션 | 실리콘-유기 엘라스토머 겔 |
| JP2008069210A (ja) * | 2006-09-12 | 2008-03-27 | Shin Etsu Chem Co Ltd | 多環式炭化水素基含有シリコーン系硬化性組成物 |
| US7863365B2 (en) | 2006-12-20 | 2011-01-04 | Freudenberg-Nok General Partnership | Robust magnetizable elastomeric thermoplastic blends |
| WO2008085360A2 (en) * | 2006-12-29 | 2008-07-17 | Dow Corning Corporation | Personal care compositions containing silicone elastomer gels |
| DE102009025981A1 (de) * | 2009-06-16 | 2011-03-31 | Saertex Gmbh & Co. Kg | Verfahren zur Herstellung eines textilen Halbzeugs mit verbesserter Zähigkeit und textiles Halbzeug |
| JP5695372B2 (ja) * | 2010-09-03 | 2015-04-01 | 株式会社カネカ | オルガノポリシロキサン系組成物および硬化物 |
| JP5919361B2 (ja) * | 2014-11-18 | 2016-05-18 | 株式会社カネカ | オルガノポリシロキサン系組成物および硬化物 |
| KR102798860B1 (ko) * | 2018-12-21 | 2025-04-25 | 다우 실리콘즈 코포레이션 | 다작용성 유기실록산, 이를 함유하는 조성물, 및 이의 제조 방법 |
Family Cites Families (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4657981A (en) * | 1962-05-14 | 1987-04-14 | Hercules Incorporated | Dicyclopentadiene polymer containing elastomer |
| US4902731A (en) * | 1986-08-27 | 1990-02-20 | Hercules Incorporated | Organosilicon prepolymers |
| US4900779A (en) * | 1986-08-27 | 1990-02-13 | Hercules Incorporated | Organosilicon polymers |
| DE3631125A1 (de) * | 1986-09-12 | 1988-03-24 | Wacker Chemie Gmbh | Verfahren zur herstellung von organopolysiloxanelastomeren und neue organosiliciumverbindungen |
| US4877820A (en) | 1987-03-20 | 1989-10-31 | Hercules Incorporated | Cross-linked organosiloxane polymers |
| DE3855943T2 (de) * | 1987-03-20 | 1997-10-02 | Hercules Inc | Vernetzte Organosiloxanpolymer |
| JPS63251464A (ja) * | 1987-04-08 | 1988-10-18 | Toray Silicone Co Ltd | 導電性シリコ−ンゴム粒状物 |
| JPH0768389B2 (ja) * | 1987-07-07 | 1995-07-26 | 東レ・ダウコーニング・シリコーン株式会社 | 非粘着性シリコ−ンゲル成形体 |
| US5013809A (en) * | 1987-07-30 | 1991-05-07 | Hercules Incorporated | Organosilicon compositions |
| US5077134A (en) * | 1989-10-10 | 1991-12-31 | Hercules Incorporated | Organosilicon compositions |
| US5068303A (en) * | 1989-10-16 | 1991-11-26 | Hercules Incorporated | Organosilicon materials |
| US5008360A (en) * | 1989-10-16 | 1991-04-16 | Hercules Incorporated | Organosilicon materials |
| US5025048A (en) * | 1990-04-12 | 1991-06-18 | Hercules Incorporated | Organosilicon composition comprising stabilizer |
| US5118735A (en) * | 1990-10-05 | 1992-06-02 | Hercules Incorporated | Organosilicon composition comprising stabilizers |
-
1991
- 1991-04-15 US US07/685,360 patent/US5171817A/en not_active Expired - Lifetime
-
1992
- 1992-03-31 CA CA002064386A patent/CA2064386A1/en not_active Abandoned
- 1992-04-07 EP EP92105988A patent/EP0509373B1/en not_active Expired - Lifetime
- 1992-04-07 DE DE69215950T patent/DE69215950T2/de not_active Expired - Fee Related
- 1992-04-13 TW TW081102846A patent/TW208036B/zh active
- 1992-04-14 KR KR1019920006213A patent/KR100192721B1/ko not_active Expired - Fee Related
- 1992-04-15 JP JP09516392A patent/JP3288423B2/ja not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| JP3288423B2 (ja) | 2002-06-04 |
| US5171817A (en) | 1992-12-15 |
| EP0509373A2 (en) | 1992-10-21 |
| KR100192721B1 (ko) | 1999-06-15 |
| KR920019881A (ko) | 1992-11-20 |
| EP0509373B1 (en) | 1996-12-18 |
| TW208036B (enExample) | 1993-06-21 |
| DE69215950D1 (de) | 1997-01-30 |
| EP0509373A3 (en) | 1993-02-17 |
| DE69215950T2 (de) | 1997-04-03 |
| JPH06306174A (ja) | 1994-11-01 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| EEER | Examination request | ||
| FZDE | Discontinued |