SI9200319A - Polymeric dispersants and filled compositions containing them - Google Patents

Polymeric dispersants and filled compositions containing them Download PDF

Info

Publication number: SI9200319A
Authority: SI; Slovenia
Prior art keywords: polymer; curable composition; polymeric; group; organic liquid
Prior art date: 1991-11-15

Application number

SI19929200319A

Other languages

English (en)

Slovenian (sl)

Inventor

David Piers Ashton

Geraldine Anne Moorman

Roger Norman Rothon

Original Assignee

Imperial Chemical Industries Plc

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.)

1991-11-15

Filing date

1992-11-13

Publication date

1993-06-30

1991-11-15 Priority claimed from GB919124307A external-priority patent/GB9124307D0/en

1991-11-15 Priority claimed from GB919124305A external-priority patent/GB9124305D0/en

1991-11-15 Priority claimed from GB919124309A external-priority patent/GB9124309D0/en

1992-11-13 Application filed by Imperial Chemical Industries Plc filed Critical Imperial Chemical Industries Plc

1993-06-30 Publication of SI9200319A publication Critical patent/SI9200319A/sl

Links

239000000203 mixture Substances 0.000 title claims abstract description 93
239000002270 dispersing agent Substances 0.000 title claims abstract description 50
229920000642 polymer Polymers 0.000 claims abstract description 56
239000011256 inorganic filler Substances 0.000 claims abstract description 23
229910003475 inorganic filler Inorganic materials 0.000 claims abstract description 23
239000002131 composite material Substances 0.000 claims abstract description 15
239000005062 Polybutadiene Substances 0.000 claims abstract description 14
229920002857 polybutadiene Polymers 0.000 claims abstract description 14
238000005382 thermal cycling Methods 0.000 claims abstract description 3
239000007788 liquid Substances 0.000 claims description 47
VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 41
239000002245 particle Substances 0.000 claims description 28
239000000945 filler Substances 0.000 claims description 27
239000000178 monomer Substances 0.000 claims description 26
239000000463 material Substances 0.000 claims description 20
239000010453 quartz Substances 0.000 claims description 17
-1 hydroxyl ester Chemical class 0.000 claims description 16
125000000524 functional group Chemical group 0.000 claims description 10
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 8
229920000193 polymethacrylate Polymers 0.000 claims description 8
150000008064 anhydrides Chemical class 0.000 claims description 7
229920001400 block copolymer Polymers 0.000 claims description 7
229920000098 polyolefin Polymers 0.000 claims description 7
CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 6
125000004432 carbon atom Chemical group C* 0.000 claims description 6
239000007787 solid Substances 0.000 claims description 6
XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 5
NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 5
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 5
229910052710 silicon Inorganic materials 0.000 claims description 5
239000010703 silicon Substances 0.000 claims description 5
239000004593 Epoxy Substances 0.000 claims description 4
238000006243 chemical reaction Methods 0.000 claims description 4
229920005862 polyol Polymers 0.000 claims description 4
150000003077 polyols Chemical class 0.000 claims description 4
239000012686 silicon precursor Substances 0.000 claims description 4
238000007711 solidification Methods 0.000 claims description 4
230000008023 solidification Effects 0.000 claims description 4
125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 3
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150000001412 amines Chemical class 0.000 claims description 3
150000001993 dienes Chemical class 0.000 claims description 3
230000009477 glass transition Effects 0.000 claims description 3
229910052736 halogen Inorganic materials 0.000 claims description 3
125000001183 hydrocarbyl group Chemical group 0.000 claims description 3
125000005397 methacrylic acid ester group Chemical group 0.000 claims description 3
FZHAPNGMFPVSLP-UHFFFAOYSA-N silanamine Chemical compound [SiH3]N FZHAPNGMFPVSLP-UHFFFAOYSA-N 0.000 claims description 3
239000000126 substance Substances 0.000 claims description 3
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
239000000654 additive Substances 0.000 claims description 2
150000001408 amides Chemical class 0.000 claims description 2
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229920006037 cross link polymer Polymers 0.000 claims description 2
150000002367 halogens Chemical class 0.000 claims description 2
229910052739 hydrogen Inorganic materials 0.000 claims description 2
239000001257 hydrogen Substances 0.000 claims description 2
150000003949 imides Chemical class 0.000 claims description 2
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239000002243 precursor Substances 0.000 claims description 2
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125000003700 epoxy group Chemical group 0.000 claims 1
150000002148 esters Chemical class 0.000 claims 1
125000005843 halogen group Chemical group 0.000 claims 1
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238000012360 testing method Methods 0.000 description 38
239000006185 dispersion Substances 0.000 description 28
238000000034 method Methods 0.000 description 26
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VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 24
239000000047 product Substances 0.000 description 20
230000009172 bursting Effects 0.000 description 18
230000006378 damage Effects 0.000 description 18
229920002633 Kraton (polymer) Polymers 0.000 description 13
STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Substances CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 description 13
DBCAQXHNJOFNGC-UHFFFAOYSA-N 4-bromo-1,1,1-trifluorobutane Chemical compound FC(F)(F)CCCBr DBCAQXHNJOFNGC-UHFFFAOYSA-N 0.000 description 12
229910052906 cristobalite Inorganic materials 0.000 description 12
239000003054 catalyst Substances 0.000 description 11
235000021355 Stearic acid Nutrition 0.000 description 10
239000004615 ingredient Substances 0.000 description 10
QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 10
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208000027418 Wounds and injury Diseases 0.000 description 9
208000014674 injury Diseases 0.000 description 9
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239000000470 constituent Substances 0.000 description 8
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238000006116 polymerization reaction Methods 0.000 description 7
IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 6
239000011159 matrix material Substances 0.000 description 6
239000010445 mica Substances 0.000 description 6
229910052618 mica group Inorganic materials 0.000 description 6
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230000000052 comparative effect Effects 0.000 description 5
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239000002861 polymer material Substances 0.000 description 5
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238000003756 stirring Methods 0.000 description 5
238000010998 test method Methods 0.000 description 5
NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 4
229920001577 copolymer Polymers 0.000 description 4
229920001519 homopolymer Polymers 0.000 description 4
FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 4
229920003229 poly(methyl methacrylate) Polymers 0.000 description 4
239000004926 polymethyl methacrylate Substances 0.000 description 4
229920002554 vinyl polymer Polymers 0.000 description 4
WYTZZXDRDKSJID-UHFFFAOYSA-N (3-aminopropyl)triethoxysilane Chemical compound CCO[Si](OCC)(OCC)CCCN WYTZZXDRDKSJID-UHFFFAOYSA-N 0.000 description 3
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 3
KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 3
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 3
229910052626 biotite Inorganic materials 0.000 description 3
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 3
239000003795 chemical substances by application Substances 0.000 description 3
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FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 3
238000003860 storage Methods 0.000 description 3
PSGCQDPCAWOCSH-UHFFFAOYSA-N (4,7,7-trimethyl-3-bicyclo[2.2.1]heptanyl) prop-2-enoate Chemical compound C1CC2(C)C(OC(=O)C=C)CC1C2(C)C PSGCQDPCAWOCSH-UHFFFAOYSA-N 0.000 description 2
JKNCOURZONDCGV-UHFFFAOYSA-N 2-(dimethylamino)ethyl 2-methylprop-2-enoate Chemical compound CN(C)CCOC(=O)C(C)=C JKNCOURZONDCGV-UHFFFAOYSA-N 0.000 description 2
INQDDHNZXOAFFD-UHFFFAOYSA-N 2-[2-(2-prop-2-enoyloxyethoxy)ethoxy]ethyl prop-2-enoate Chemical compound C=CC(=O)OCCOCCOCCOC(=O)C=C INQDDHNZXOAFFD-UHFFFAOYSA-N 0.000 description 2
SZTBMYHIYNGYIA-UHFFFAOYSA-N 2-chloroacrylic acid Chemical compound OC(=O)C(Cl)=C SZTBMYHIYNGYIA-UHFFFAOYSA-N 0.000 description 2
KUDUQBURMYMBIJ-UHFFFAOYSA-N 2-prop-2-enoyloxyethyl prop-2-enoate Chemical compound C=CC(=O)OCCOC(=O)C=C KUDUQBURMYMBIJ-UHFFFAOYSA-N 0.000 description 2
PNEYBMLMFCGWSK-UHFFFAOYSA-N Alumina Chemical class [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
229930185605 Bisphenol Natural products 0.000 description 2
BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 2
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 2
239000005977 Ethylene Substances 0.000 description 2
125000003118 aryl group Chemical group 0.000 description 2
230000008901 benefit Effects 0.000 description 2
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238000001816 cooling Methods 0.000 description 2
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238000010168 coupling process Methods 0.000 description 2
238000005859 coupling reaction Methods 0.000 description 2
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239000003822 epoxy resin Substances 0.000 description 2
238000011049 filling Methods 0.000 description 2
238000010438 heat treatment Methods 0.000 description 2
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
238000004519 manufacturing process Methods 0.000 description 2
229910052751 metal Inorganic materials 0.000 description 2
239000002184 metal Substances 0.000 description 2
238000000465 moulding Methods 0.000 description 2
229920001515 polyalkylene glycol Polymers 0.000 description 2
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238000002076 thermal analysis method Methods 0.000 description 2
230000009974 thixotropic effect Effects 0.000 description 2
230000007704 transition Effects 0.000 description 2
QQQSFSZALRVCSZ-UHFFFAOYSA-N triethoxysilane Chemical compound CCO[SiH](OCC)OCC QQQSFSZALRVCSZ-UHFFFAOYSA-N 0.000 description 2
RRKODOZNUZCUBN-CCAGOZQPSA-N (1z,3z)-cycloocta-1,3-diene Chemical compound C1CC\C=C/C=C\C1 RRKODOZNUZCUBN-CCAGOZQPSA-N 0.000 description 1
XQWPAXMLSPUNPV-UHFFFAOYSA-N (4-tert-butylcyclohexyl) (4-tert-butylcyclohexyl)oxy carbonate Chemical compound C1CC(C(C)(C)C)CCC1OOC(=O)OC1CCC(C(C)(C)C)CC1 XQWPAXMLSPUNPV-UHFFFAOYSA-N 0.000 description 1
NOBYOEQUFMGXBP-UHFFFAOYSA-N (4-tert-butylcyclohexyl) (4-tert-butylcyclohexyl)oxycarbonyloxy carbonate Chemical compound C1CC(C(C)(C)C)CCC1OC(=O)OOC(=O)OC1CCC(C(C)(C)C)CC1 NOBYOEQUFMGXBP-UHFFFAOYSA-N 0.000 description 1
VDYWHVQKENANGY-UHFFFAOYSA-N 1,3-Butyleneglycol dimethacrylate Chemical compound CC(=C)C(=O)OC(C)CCOC(=O)C(C)=C VDYWHVQKENANGY-UHFFFAOYSA-N 0.000 description 1
RSNDTPFSMDVWCS-UHFFFAOYSA-N 2-(butoxymethyl)prop-2-enamide Chemical compound CCCCOCC(=C)C(N)=O RSNDTPFSMDVWCS-UHFFFAOYSA-N 0.000 description 1
NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical group CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 1
HWSSEYVMGDIFMH-UHFFFAOYSA-N 2-[2-[2-(2-methylprop-2-enoyloxy)ethoxy]ethoxy]ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCOCCOC(=O)C(C)=C HWSSEYVMGDIFMH-UHFFFAOYSA-N 0.000 description 1
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UTSSRHLQDCZZDO-UHFFFAOYSA-N 2-ethoxyethoxy 2-ethoxyethyl carbonate Chemical compound CCOCCOOC(=O)OCCOCC UTSSRHLQDCZZDO-UHFFFAOYSA-N 0.000 description 1
ZACVGCNKGYYQHA-UHFFFAOYSA-N 2-ethylhexoxycarbonyloxy 2-ethylhexyl carbonate Chemical compound CCCCC(CC)COC(=O)OOC(=O)OCC(CC)CCCC ZACVGCNKGYYQHA-UHFFFAOYSA-N 0.000 description 1
IISCRELTMNKFMH-UHFFFAOYSA-N 2-methoxypropan-2-yl 2-methoxypropan-2-yloxycarbonyloxy carbonate Chemical compound COC(C)(C)OC(=O)OOC(=O)OC(C)(C)OC IISCRELTMNKFMH-UHFFFAOYSA-N 0.000 description 1
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FQMIAEWUVYWVNB-UHFFFAOYSA-N 3-prop-2-enoyloxybutyl prop-2-enoate Chemical compound C=CC(=O)OC(C)CCOC(=O)C=C FQMIAEWUVYWVNB-UHFFFAOYSA-N 0.000 description 1
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238000004438 BET method Methods 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
239000004215 Carbon black (E152) Substances 0.000 description 1
BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 1
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239000004372 Polyvinyl alcohol Substances 0.000 description 1
BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical group [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
DAKWPKUUDNSNPN-UHFFFAOYSA-N Trimethylolpropane triacrylate Chemical compound C=CC(=O)OCC(CC)(COC(=O)C=C)COC(=O)C=C DAKWPKUUDNSNPN-UHFFFAOYSA-N 0.000 description 1
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IAXXETNIOYFMLW-COPLHBTASA-N [(1s,3s,4s)-4,7,7-trimethyl-3-bicyclo[2.2.1]heptanyl] 2-methylprop-2-enoate Chemical compound C1C[C@]2(C)[C@@H](OC(=O)C(=C)C)C[C@H]1C2(C)C IAXXETNIOYFMLW-COPLHBTASA-N 0.000 description 1
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QUZSUMLPWDHKCJ-UHFFFAOYSA-N bisphenol A dimethacrylate Chemical compound C1=CC(OC(=O)C(=C)C)=CC=C1C(C)(C)C1=CC=C(OC(=O)C(C)=C)C=C1 QUZSUMLPWDHKCJ-UHFFFAOYSA-N 0.000 description 1
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OIWOHHBRDFKZNC-UHFFFAOYSA-N cyclohexyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC1CCCCC1 OIWOHHBRDFKZNC-UHFFFAOYSA-N 0.000 description 1
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150000003944 halohydrins Chemical class 0.000 description 1
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150000002432 hydroperoxides Chemical class 0.000 description 1
238000006459 hydrosilylation reaction Methods 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
150000004679 hydroxides Chemical class 0.000 description 1
238000009863 impact test Methods 0.000 description 1
239000003112 inhibitor Substances 0.000 description 1
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239000006082 mold release agent Substances 0.000 description 1
GYVGXEWAOAAJEU-UHFFFAOYSA-N n,n,4-trimethylaniline Chemical compound CN(C)C1=CC=C(C)C=C1 GYVGXEWAOAAJEU-UHFFFAOYSA-N 0.000 description 1
YOZHLACIXDCHPV-UHFFFAOYSA-N n-(methoxymethyl)-2-methylprop-2-enamide Chemical compound COCNC(=O)C(C)=C YOZHLACIXDCHPV-UHFFFAOYSA-N 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
SRSFOMHQIATOFV-UHFFFAOYSA-N octanoyl octaneperoxoate Chemical compound CCCCCCCC(=O)OOC(=O)CCCCCCC SRSFOMHQIATOFV-UHFFFAOYSA-N 0.000 description 1
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230000002085 persistent effect Effects 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
QIWKUEJZZCOPFV-UHFFFAOYSA-N phenyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC1=CC=CC=C1 QIWKUEJZZCOPFV-UHFFFAOYSA-N 0.000 description 1
235000021317 phosphate Nutrition 0.000 description 1
150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
239000000049 pigment Substances 0.000 description 1
238000013001 point bending Methods 0.000 description 1
230000000379 polymerizing effect Effects 0.000 description 1
229920001296 polysiloxane Polymers 0.000 description 1
229920001343 polytetrafluoroethylene Polymers 0.000 description 1
239000004810 polytetrafluoroethylene Substances 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
230000002028 premature Effects 0.000 description 1
VFHDDANHQLKHJQ-UHFFFAOYSA-N prop-2-enoic acid Chemical compound OC(=O)C=C.OC(=O)C=C.OC(=O)C=C VFHDDANHQLKHJQ-UHFFFAOYSA-N 0.000 description 1
HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
BOQSSGDQNWEFSX-UHFFFAOYSA-N propan-2-yl 2-methylprop-2-enoate Chemical compound CC(C)OC(=O)C(C)=C BOQSSGDQNWEFSX-UHFFFAOYSA-N 0.000 description 1
BWJUFXUULUEGMA-UHFFFAOYSA-N propan-2-yl propan-2-yloxycarbonyloxy carbonate Chemical compound CC(C)OC(=O)OOC(=O)OC(C)C BWJUFXUULUEGMA-UHFFFAOYSA-N 0.000 description 1
YPVDWEHVCUBACK-UHFFFAOYSA-N propoxycarbonyloxy propyl carbonate Chemical compound CCCOC(=O)OOC(=O)OCCC YPVDWEHVCUBACK-UHFFFAOYSA-N 0.000 description 1
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
238000005086 pumping Methods 0.000 description 1
239000011347 resin Substances 0.000 description 1
229920005989 resin Polymers 0.000 description 1
239000004576 sand Substances 0.000 description 1
238000004062 sedimentation Methods 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
239000002210 silicon-based material Substances 0.000 description 1
239000012265 solid product Substances 0.000 description 1
239000004575 stone Substances 0.000 description 1
229920006132 styrene block copolymer Polymers 0.000 description 1
150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
239000013589 supplement Substances 0.000 description 1
239000006188 syrup Substances 0.000 description 1
235000020357 syrup Nutrition 0.000 description 1
CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 description 1
230000008719 thickening Effects 0.000 description 1
150000003568 thioethers Chemical class 0.000 description 1
229920001567 vinyl ester resin Polymers 0.000 description 1
238000004383 yellowing Methods 0.000 description 1

Classifications

- 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
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/34—Silicon-containing compounds
- C08K3/36—Silica
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08C—TREATMENT OR CHEMICAL MODIFICATION OF RUBBERS
- C08C19/00—Chemical modification of rubber
- C08C19/25—Incorporating silicon atoms into the molecule
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08C—TREATMENT OR CHEMICAL MODIFICATION OF RUBBERS
- C08C19/00—Chemical modification of rubber
- C08C19/30—Addition of a reagent which reacts with a hetero atom or a group containing hetero atoms of the macromolecule
- C08C19/34—Addition of a reagent which reacts with a hetero atom or a group containing hetero atoms of the macromolecule reacting with oxygen or oxygen-containing groups
- C08C19/36—Addition of a reagent which reacts with a hetero atom or a group containing hetero atoms of the macromolecule reacting with oxygen or oxygen-containing groups with carboxy radicals
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F287/00—Macromolecular compounds obtained by polymerising monomers on to block polymers
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F291/00—Macromolecular compounds obtained by polymerising monomers on to macromolecular compounds according to more than one of the groups C08F251/00 - C08F289/00
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F292/00—Macromolecular compounds obtained by polymerising monomers on to inorganic materials
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F8/00—Chemical modification by after-treatment
- C08F8/42—Introducing metal atoms or metal-containing groups
- 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
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/01—Use of inorganic substances as compounding ingredients characterized by their specific function
- C08K3/013—Fillers, pigments or reinforcing additives

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)
Materials Engineering (AREA)
Engineering & Computer Science (AREA)
Inorganic Chemistry (AREA)
Compositions Of Macromolecular Compounds (AREA)
Polymerisation Methods In General (AREA)
Dental Preparations (AREA)
Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
Pigments, Carbon Blacks, Or Wood Stains (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)

SI19929200319A 1991-11-15 1992-11-13 Polymeric dispersants and filled compositions containing them SI9200319A (en)

Applications Claiming Priority (3)

Application Number	Priority Date	Filing Date	Title
GB919124307A GB9124307D0 (en)	1991-11-15	1991-11-15	Polymeric dispersants and filled compositions containing them
GB919124305A GB9124305D0 (en)	1991-11-15	1991-11-15	Polymerisable compositions
GB919124309A GB9124309D0 (en)	1991-11-15	1991-11-15	Polymerisable compositions

Publications (1)

Publication Number	Publication Date
SI9200319A true SI9200319A (en)	1993-06-30

Family

ID=27265926

Family Applications (3)

Application Number	Title	Priority Date	Filing Date
SI19929200319A SI9200319A (en)	1991-11-15	1992-11-13	Polymeric dispersants and filled compositions containing them
SI9200320A SI9200320B (en)	1991-11-15	1992-11-13	Filled cured compositions for the preparation of thermoplastic products
SI19929200321A SI9200321A (en)	1991-11-15	1992-11-13	Filled cured compositions for the preparation of thermoplastic products

Family Applications After (2)

Application Number	Title	Priority Date	Filing Date
SI9200320A SI9200320B (en)	1991-11-15	1992-11-13	Filled cured compositions for the preparation of thermoplastic products
SI19929200321A SI9200321A (en)	1991-11-15	1992-11-13	Filled cured compositions for the preparation of thermoplastic products

Country Status (16)

Country	Link
US (3)	US5519083A (de)
EP (3)	EP0612328B1 (de)
JP (3)	JPH07501097A (de)
AT (3)	ATE198615T1 (de)
AU (3)	AU668369B2 (de)
CA (3)	CA2123429C (de)
DE (3)	DE69231635T2 (de)
DK (1)	DK0612328T3 (de)
ES (3)	ES2141113T3 (de)
GB (3)	GB9223602D0 (de)
GR (3)	GR3022214T3 (de)
NZ (3)	NZ245122A (de)
PT (3)	PT101056B (de)
SI (3)	SI9200319A (de)
TW (3)	TW224482B (de)
WO (3)	WO1993010159A1 (de)

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ATE198615T1 (de) *	1991-11-15	2001-01-15	Ici Plc	Polymerisierbare zusammensetzungen
TW321658B (de) *	1992-09-17	1997-12-01	Ciba Sc Holding Ag
DE4407321A1 (de) *	1994-03-04	1995-09-07	Blanco Gmbh & Co Kg	Kunststofformteile mit einer mit anorganischen Füllstoffen gefüllten Kunststoffmatrix
US5679773A (en) *	1995-01-17	1997-10-21	Affymax Technologies N.V	Reagants and methods for immobilized polymer synthesis and display
JPH10507160A (ja) *	1994-06-23	1998-07-14	アフィマックステクノロジーズエヌ．ブイ．	光活性化合物およびその使用方法
DE4441691C5 (de) *	1994-11-23	2006-01-26	Quarzwerke Gmbh	Verwendung eines feinkörnigen Quarzsandprodukts
US5624711A (en) *	1995-04-27	1997-04-29	Affymax Technologies, N.V.	Derivatization of solid supports and methods for oligomer synthesis
US5852108A (en) *	1995-05-10	1998-12-22	Toray Industries, Inc.	Composite particulate material for resin reinforcement, production thereof, and reinforced resin composition incorporated therewith
JP3701480B2 (ja) *	1998-10-22	2005-09-28	株式会社ドペル	高硬度軟質複合材
KR100312176B1 (ko) *	1999-03-23	2001-11-14	김충섭	알콕시 실란으로 치환된 디엔 공중합체 및 유기·무기 하이브리드 조성물
DE19949461A1 (de) *	1999-10-14	2001-04-26	Blanco Gmbh & Co Kg	Aushärtbare Gießmasse und unter Verwendung solcher Gießmassen hergestellte Kunststoffformkörper
IT1318503B1 (it) *	2000-05-08	2003-08-27	Elleci Srl	Materiale composito termoindurente, particolarmente adatto per larealizzazione di articoli sanitari e lavelli da cucina, e relativo
US7056984B2 (en) *	2001-05-15	2006-06-06	Mitsubishi Gas Chemical Co., Inc.	Acrylic syrup and method of producing same
JP2005504140A (ja) *	2001-09-25	2005-02-10	スリーエムイノベイティブプロパティズカンパニー	硬化性分散剤
GB0201137D0 (en) *	2002-01-18	2002-03-06	Ineos Acrylics Uk Ltd	Acrylic composition
US6838536B2 (en) *	2002-08-30	2005-01-04	Ucb, S.A.	Reactive and gel-free compositions for making hybrid composites
US6809155B2 (en) *	2002-11-20	2004-10-26	National Starch And Chemical Investment Holding Corporation	Unsaturated compounds containing silane, electron donor and electron acceptor functionality
US6784025B2 (en) *	2002-11-20	2004-08-31	National Starch And Chemical Investment Holding Corporation	Semiconductor package with a die attach adhesive having silane functionality
US7247667B2 (en) *	2004-03-23	2007-07-24	E. I. Du Pont De Nemours And Company	Particle containing solid surface material
JP4714432B2 (ja) *	2004-07-09	2011-06-29	スリーエムイノベイティブプロパティズカンパニー	熱伝導性シート
JP4869584B2 (ja) *	2004-12-03	2012-02-08	スリーエムイノベイティブプロパティズカンパニー	熱伝導性シート及びその製造方法
DE102008046569A1 (de) *	2008-09-05	2010-03-11	Blanco Gmbh + Co Kg	Aushärtbare Gießmasse zur Herstellung von Kunststoffformteilen
EP2379298B1 (de) *	2008-11-20	2012-10-31	Allergan, Inc.	System und verfahren zum formen von weichen, fluidgefüllten implantatschalen
JP2010218597A (ja) *	2009-03-13	2010-09-30	Toshiba Corp	パターン転写用樹脂スタンパ、及びこれを用いた磁気記録媒体の製造方法
JP2010218605A (ja) *	2009-03-13	2010-09-30	Toshiba Corp	パターン転写用紫外線硬化性樹脂材料、及びこれを用いた磁気記録媒体の製造方法
JP4543117B1 (ja) *	2009-03-13	2010-09-15	株式会社東芝	パターン転写用紫外線硬化性樹脂材料、及びこれを用いた磁気記録媒体の製造方法
JP4729114B2 (ja) *	2009-03-18	2011-07-20	株式会社東芝	磁気記録媒体の製造方法
KR20190058478A (ko)	2016-09-29	2019-05-29	닛토덴코 가부시키가이샤	구조물 상의 도막, 도막을 형성하기 위한 도료 세트 및 하도층용 도료 그리고 도공 방법
DE102020119386A1 (de) *	2020-07-22	2022-01-27	Schock Gmbh	Wärmeaushärtbare biobasierte Gießmasse, hieraus hergestellter Formkörper sowie Verfahren zur Herstellung eines solchen Formkörpers
DE102021200091A1 (de)	2021-01-07	2022-07-07	Blanco Gmbh + Co Kg	Aushärtbare Gießmasse zur Herstellung von Kunststoffformteilen

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US3981851A (en) *	1972-01-10	1976-09-21	Dow Corning Corporation	Primer compositions
GB1493393A (en) *	1974-05-29	1977-11-30	Ici Ltd	Fluid curable compositions containing particulate fillers and composite polymeric materials obtained therefrom
US4221697A (en) *	1974-05-29	1980-09-09	Imperial Chemical Industries Limited	Composite materials
US4146529A (en) *	1976-03-29	1979-03-27	Toa Nenryo Kogyo Kabushiki Kaisha	Process for the production of modified polyolefin
US4598123A (en) *	1983-07-14	1986-07-01	Unites States Steel Corporation	Impact modified methyl methacrylate polymer
DE3531913A1 (de) *	1985-09-07	1987-03-19	Roehm Gmbh	Haertbare giessharze
US4783504A (en) *	1986-02-28	1988-11-08	Shell Oil Company	Hot melt adhesive containing a silane grafted hydrogenated block polymer
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USH758H (en) *	1987-12-23	1990-04-03		Sealant composition
JP2750135B2 (ja) *	1988-11-29	1998-05-13	サンスター技研株式会社	湿気架橋型ポリオレフィン用プライマー
GB8907211D0 (en) *	1989-03-30	1989-05-10	Ici Plc	Composite materials
GB9110883D0 (en) *	1991-05-20	1991-07-10	Ici Plc	Highly filled,polymerisable compositions
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ATE198615T1 (de) *	1991-11-15	2001-01-15	Ici Plc	Polymerisierbare zusammensetzungen
US5283288A (en) *	1992-01-07	1994-02-01	Ciba Corning Diagnostics Corp.	PVC coatings for electrodes

1992
- 1992-11-11 AT AT92922894T patent/ATE198615T1/de active
- 1992-11-11 GB GB929223602A patent/GB9223602D0/en active Pending
- 1992-11-11 AU AU29065/92A patent/AU668369B2/en not_active Ceased
- 1992-11-11 AT AT92923015T patent/ATE188980T1/de not_active IP Right Cessation
- 1992-11-11 ES ES92923015T patent/ES2141113T3/es not_active Expired - Lifetime
- 1992-11-11 JP JP50906693A patent/JPH07501097A/ja active Pending
- 1992-11-11 CA CA002123429A patent/CA2123429C/en not_active Expired - Lifetime
- 1992-11-11 US US08/204,181 patent/US5519083A/en not_active Expired - Lifetime
- 1992-11-11 AU AU29053/92A patent/AU657180B2/en not_active Ceased
- 1992-11-11 US US08/244,264 patent/US5530064A/en not_active Expired - Lifetime
- 1992-11-11 GB GB929223628A patent/GB9223628D0/en active Pending
- 1992-11-11 DE DE69231635T patent/DE69231635T2/de not_active Expired - Lifetime
- 1992-11-11 WO PCT/GB1992/002079 patent/WO1993010159A1/en not_active Ceased
- 1992-11-11 ES ES92922894T patent/ES2155063T3/es not_active Expired - Lifetime
- 1992-11-11 ES ES92922920T patent/ES2096108T3/es not_active Expired - Lifetime
- 1992-11-11 WO PCT/GB1992/002080 patent/WO1993010182A1/en not_active Ceased
- 1992-11-11 DK DK92922920.1T patent/DK0612328T3/da active
- 1992-11-11 EP EP92922920A patent/EP0612328B1/de not_active Expired - Lifetime
- 1992-11-11 DE DE69230587T patent/DE69230587T2/de not_active Expired - Fee Related
- 1992-11-11 AU AU29032/92A patent/AU665380B2/en not_active Ceased
- 1992-11-11 EP EP92922894A patent/EP0612333B1/de not_active Expired - Lifetime
- 1992-11-11 CA CA002121469A patent/CA2121469C/en not_active Expired - Lifetime
- 1992-11-11 DE DE69216427T patent/DE69216427T2/de not_active Expired - Lifetime
- 1992-11-11 EP EP92923015A patent/EP0612334B1/de not_active Expired - Lifetime
- 1992-11-11 CA CA002121468A patent/CA2121468A1/en not_active Abandoned
- 1992-11-11 JP JP5509067A patent/JPH07501098A/ja active Pending
- 1992-11-11 WO PCT/GB1992/002081 patent/WO1993010183A1/en not_active Ceased
- 1992-11-11 AT AT92922920T patent/ATE147082T1/de active
- 1992-11-11 GB GB929223629A patent/GB9223629D0/en active Pending
- 1992-11-11 JP JP05509068A patent/JP3133334B2/ja not_active Expired - Fee Related
- 1992-11-13 SI SI19929200319A patent/SI9200319A/sl unknown
- 1992-11-13 NZ NZ245122A patent/NZ245122A/en unknown
- 1992-11-13 NZ NZ245120A patent/NZ245120A/en unknown
- 1992-11-13 SI SI9200320A patent/SI9200320B/sl unknown
- 1992-11-13 NZ NZ245121A patent/NZ245121A/en unknown
- 1992-11-13 SI SI19929200321A patent/SI9200321A/sl unknown
- 1992-11-13 PT PT101056A patent/PT101056B/pt not_active IP Right Cessation
- 1992-11-13 PT PT101055A patent/PT101055B/pt not_active IP Right Cessation
- 1992-11-13 PT PT101054A patent/PT101054B/pt not_active IP Right Cessation
- 1992-12-18 TW TW081110208A patent/TW224482B/zh not_active IP Right Cessation
- 1992-12-18 TW TW081110199A patent/TW270135B/zh active
- 1992-12-18 TW TW081110186A patent/TW226390B/zh not_active IP Right Cessation
1995
- 1995-06-05 US US08/462,067 patent/US5578673A/en not_active Expired - Lifetime
1997
- 1997-01-03 GR GR960403577T patent/GR3022214T3/el unknown
2000
- 2000-03-22 GR GR20000400716T patent/GR3033030T3/el not_active IP Right Cessation
2001
- 2001-04-10 GR GR20010400594T patent/GR3035740T3/el unknown

Also Published As

Publication number	Publication date
CA2121468A1 (en)	1993-05-27
AU668369B2 (en)	1996-05-02
TW226390B (de)	1994-07-11
WO1993010183A1 (en)	1993-05-27
TW270135B (en)	1996-02-11
EP0612333A1 (de)	1994-08-31
CA2123429C (en)	2004-05-25
AU2906592A (en)	1993-06-15
ATE188980T1 (de)	2000-02-15
ATE147082T1 (de)	1997-01-15
WO1993010159A1 (en)	1993-05-27
ES2141113T3 (es)	2000-03-16
PT101054A (pt)	1994-02-28
GR3022214T3 (en)	1997-04-30
EP0612333B1 (de)	2001-01-10
TW224482B (de)	1994-06-01
NZ245121A (en)	1995-04-27
US5519083A (en)	1996-05-21
SI9200321A (en)	1993-06-30
JPH07501097A (ja)	1995-02-02
DE69231635D1 (de)	2001-02-15
CA2121469A1 (en)	1993-05-27
PT101055B (pt)	1999-10-29
PT101054B (pt)	1999-07-30
US5578673A (en)	1996-11-26
CA2123429A1 (en)	1993-05-27
AU2905392A (en)	1993-06-15
US5530064A (en)	1996-06-25
PT101055A (pt)	1994-02-28
CA2121469C (en)	2003-09-16
EP0612334B1 (de)	2000-01-19
PT101056B (pt)	1999-07-30
DE69216427D1 (de)	1997-02-13
NZ245122A (en)	1995-10-26
JPH07501099A (ja)	1995-02-02
DE69230587T2 (de)	2000-08-03
NZ245120A (en)	1995-12-21
EP0612334A1 (de)	1994-08-31
AU665380B2 (en)	1996-01-04
DK0612328T3 (da)	1997-06-30
JPH07501098A (ja)	1995-02-02
ES2096108T3 (es)	1997-03-01
SI9200320B (en)	2001-04-30
WO1993010182A1 (en)	1993-05-27
SI9200320A (en)	1993-06-30
DE69216427T2 (de)	1997-05-15
GR3033030T3 (en)	2000-08-31
GB9223602D0 (en)	1992-12-23
GB9223628D0 (en)	1992-12-23
DE69230587D1 (de)	2000-02-24
GB9223629D0 (en)	1992-12-23
AU657180B2 (en)	1995-03-02
ATE198615T1 (de)	2001-01-15
AU2903292A (en)	1993-06-15
EP0612328B1 (de)	1997-01-02
DE69231635T2 (de)	2001-08-16
JP3133334B2 (ja)	2001-02-05
ES2155063T3 (es)	2001-05-01
GR3035740T3 (en)	2001-07-31
PT101056A (pt)	1994-02-28
EP0612328A1 (de)	1994-08-31

Legal Events

Date	Code	Title	Description
2005-01-10	IF	Valid on the event date

Publication	Publication Date	Title
EP0612328B1 (de)	1997-01-02	Polmerisierbare zusammensetzungen
US4786660A (en)	1988-11-22	Method for making curable casting resins
Wei et al.	1998	Novel organic–inorganic chemical hybrid fillers for dental composite materials
JPH0418453A (ja)	1992-01-22	有機―無機複合粉体及び該粉体の製造方法
CH508674A (de)	1971-06-15	Verstärkte Polymermischung und Verfahren zu ihrer Herstellung
US5519081A (en)	1996-05-21	Polymerisable compositions
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