SI9200321A - Filled cured compositions for the preparation of thermoplastic products - Google Patents
Filled cured compositions for the preparation of thermoplastic products Download PDFInfo
- Publication number
- SI9200321A SI9200321A SI19929200321A SI9200321A SI9200321A SI 9200321 A SI9200321 A SI 9200321A SI 19929200321 A SI19929200321 A SI 19929200321A SI 9200321 A SI9200321 A SI 9200321A SI 9200321 A SI9200321 A SI 9200321A
- Authority
- SI
- Slovenia
- Prior art keywords
- curable composition
- composition according
- organic liquid
- polymeric material
- polymer
- Prior art date
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- 239000000203 mixture Substances 0.000 title claims abstract description 90
- 238000002360 preparation method Methods 0.000 title claims description 4
- 229920001169 thermoplastic Polymers 0.000 title 1
- 239000004416 thermosoftening plastic Substances 0.000 title 1
- 229920000642 polymer Polymers 0.000 claims abstract description 38
- 239000011256 inorganic filler Substances 0.000 claims abstract description 32
- 229910003475 inorganic filler Inorganic materials 0.000 claims abstract description 32
- 239000007788 liquid Substances 0.000 claims description 65
- 239000002245 particle Substances 0.000 claims description 48
- 239000000463 material Substances 0.000 claims description 46
- 239000000945 filler Substances 0.000 claims description 33
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 29
- 239000000178 monomer Substances 0.000 claims description 26
- 239000004615 ingredient Substances 0.000 claims description 25
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 claims description 16
- 238000007711 solidification Methods 0.000 claims description 15
- 230000008023 solidification Effects 0.000 claims description 15
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims description 10
- STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Substances CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 claims description 10
- DBCAQXHNJOFNGC-UHFFFAOYSA-N 4-bromo-1,1,1-trifluorobutane Chemical compound FC(F)(F)CCCBr DBCAQXHNJOFNGC-UHFFFAOYSA-N 0.000 claims description 9
- 239000010453 quartz Substances 0.000 claims description 9
- 229920000193 polymethacrylate Polymers 0.000 claims description 8
- 239000000126 substance Substances 0.000 claims description 8
- XDLMVUHYZWKMMD-UHFFFAOYSA-N 3-trimethoxysilylpropyl 2-methylprop-2-enoate Chemical compound CO[Si](OC)(OC)CCCOC(=O)C(C)=C XDLMVUHYZWKMMD-UHFFFAOYSA-N 0.000 claims description 7
- 229920001400 block copolymer Polymers 0.000 claims description 7
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 7
- 239000011159 matrix material Substances 0.000 claims description 7
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 6
- 239000000654 additive Substances 0.000 claims description 6
- 238000004873 anchoring Methods 0.000 claims description 6
- 150000001993 dienes Chemical class 0.000 claims description 6
- 229920000098 polyolefin Polymers 0.000 claims description 6
- 230000000996 additive effect Effects 0.000 claims description 5
- 239000012530 fluid Substances 0.000 claims description 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 5
- 239000000377 silicon dioxide Substances 0.000 claims description 5
- 239000007787 solid Substances 0.000 claims description 5
- 230000009477 glass transition Effects 0.000 claims description 4
- 229920005862 polyol Polymers 0.000 claims description 4
- 150000003077 polyols Chemical class 0.000 claims description 4
- 229920002554 vinyl polymer Polymers 0.000 claims description 4
- 125000001183 hydrocarbyl group Chemical group 0.000 claims description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims description 3
- 239000001257 hydrogen Substances 0.000 claims description 3
- 125000005397 methacrylic acid ester group Chemical group 0.000 claims description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- 230000008878 coupling Effects 0.000 claims description 2
- 238000010168 coupling process Methods 0.000 claims description 2
- 238000005859 coupling reaction Methods 0.000 claims description 2
- 229920006037 cross link polymer Polymers 0.000 claims description 2
- 150000002148 esters Chemical class 0.000 claims description 2
- 239000002861 polymer material Substances 0.000 claims description 2
- 239000003960 organic solvent Substances 0.000 claims 1
- 239000011435 rock Substances 0.000 claims 1
- 239000008247 solid mixture Substances 0.000 claims 1
- 239000002270 dispersing agent Substances 0.000 abstract description 17
- 239000002131 composite material Substances 0.000 abstract description 3
- 238000005382 thermal cycling Methods 0.000 abstract description 2
- 239000005062 Polybutadiene Substances 0.000 abstract 1
- 229920002857 polybutadiene Polymers 0.000 abstract 1
- 239000006185 dispersion Substances 0.000 description 34
- 238000012360 testing method Methods 0.000 description 30
- 230000006378 damage Effects 0.000 description 25
- 230000035939 shock Effects 0.000 description 25
- 230000009172 bursting Effects 0.000 description 22
- 208000027418 Wounds and injury Diseases 0.000 description 20
- 208000014674 injury Diseases 0.000 description 20
- 239000000047 product Substances 0.000 description 20
- 238000000034 method Methods 0.000 description 17
- 235000012239 silicon dioxide Nutrition 0.000 description 12
- 239000003054 catalyst Substances 0.000 description 11
- 238000005227 gel permeation chromatography Methods 0.000 description 11
- -1 CH ^ CHCICO.OH) Chemical compound 0.000 description 10
- 238000006116 polymerization reaction Methods 0.000 description 9
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 8
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 8
- 239000011230 binding agent Substances 0.000 description 7
- 230000006835 compression Effects 0.000 description 7
- 238000007906 compression Methods 0.000 description 7
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 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
- 239000000470 constituent Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 5
- 244000309466 calf Species 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 5
- 229920001577 copolymer Polymers 0.000 description 5
- 229910052906 cristobalite Inorganic materials 0.000 description 5
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 5
- 238000002156 mixing Methods 0.000 description 5
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 4
- NTXGQCSETZTARF-UHFFFAOYSA-N buta-1,3-diene;prop-2-enenitrile Chemical compound C=CC=C.C=CC#N NTXGQCSETZTARF-UHFFFAOYSA-N 0.000 description 4
- 229910002026 crystalline silica Inorganic materials 0.000 description 4
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 description 4
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 4
- 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
- 235000021355 Stearic acid Nutrition 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000000227 grinding Methods 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 3
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 3
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 3
- 239000004926 polymethyl methacrylate Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 239000008117 stearic acid Substances 0.000 description 3
- 238000003860 storage Methods 0.000 description 3
- 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 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
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical class [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 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
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 2
- 229910052804 chromium Inorganic materials 0.000 description 2
- 239000011651 chromium Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- GGSUCNLOZRCGPQ-UHFFFAOYSA-N diethylaniline Chemical compound CCN(CC)C1=CC=CC=C1 GGSUCNLOZRCGPQ-UHFFFAOYSA-N 0.000 description 2
- 239000003822 epoxy resin Substances 0.000 description 2
- 150000004679 hydroxides Chemical class 0.000 description 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
- 125000005647 linker group Chemical group 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 229920001515 polyalkylene glycol Polymers 0.000 description 2
- 229920000647 polyepoxide Polymers 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- 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
- 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 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
- LTHJXDSHSVNJKG-UHFFFAOYSA-N 2-[2-[2-[2-(2-methylprop-2-enoyloxy)ethoxy]ethoxy]ethoxy]ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCOCCOCCOC(=O)C(C)=C LTHJXDSHSVNJKG-UHFFFAOYSA-N 0.000 description 1
- 125000000022 2-aminoethyl group Chemical group [H]C([*])([H])C([H])([H])N([H])[H] 0.000 description 1
- 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
- RUMACXVDVNRZJZ-UHFFFAOYSA-N 2-methylpropyl 2-methylprop-2-enoate Chemical compound CC(C)COC(=O)C(C)=C RUMACXVDVNRZJZ-UHFFFAOYSA-N 0.000 description 1
- GNSFRPWPOGYVLO-UHFFFAOYSA-N 3-hydroxypropyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCO GNSFRPWPOGYVLO-UHFFFAOYSA-N 0.000 description 1
- 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
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 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
- 239000005046 Chlorosilane Substances 0.000 description 1
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- 229920002633 Kraton (polymer) Polymers 0.000 description 1
- GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 description 1
- CNCOEDDPFOAUMB-UHFFFAOYSA-N N-Methylolacrylamide Chemical compound OCNC(=O)C=C CNCOEDDPFOAUMB-UHFFFAOYSA-N 0.000 description 1
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 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
- OKKRPWIIYQTPQF-UHFFFAOYSA-N Trimethylolpropane trimethacrylate Chemical compound CC(=C)C(=O)OCC(CC)(COC(=O)C(C)=C)COC(=O)C(C)=C OKKRPWIIYQTPQF-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 238000012644 addition polymerization Methods 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 125000005907 alkyl ester group Chemical group 0.000 description 1
- 150000004645 aluminates Chemical class 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
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- AOJOEFVRHOZDFN-UHFFFAOYSA-N benzyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC1=CC=CC=C1 AOJOEFVRHOZDFN-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 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
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 1
- NFMLWRCAFGMYPI-UHFFFAOYSA-N butanedioic acid;2-hydroxypropanoic acid Chemical compound CC(O)C(O)=O.OC(=O)CCC(O)=O NFMLWRCAFGMYPI-UHFFFAOYSA-N 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 150000001244 carboxylic acid anhydrides Chemical class 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- KOPOQZFJUQMUML-UHFFFAOYSA-N chlorosilane Chemical class Cl[SiH3] KOPOQZFJUQMUML-UHFFFAOYSA-N 0.000 description 1
- 239000011362 coarse particle Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000010411 cooking Methods 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- OIWOHHBRDFKZNC-UHFFFAOYSA-N cyclohexyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC1CCCCC1 OIWOHHBRDFKZNC-UHFFFAOYSA-N 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
- 125000003700 epoxy group Chemical group 0.000 description 1
- 125000002573 ethenylidene group Chemical group [*]=C=C([H])[H] 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 238000005189 flocculation Methods 0.000 description 1
- 230000016615 flocculation Effects 0.000 description 1
- 229920001002 functional polymer Polymers 0.000 description 1
- 238000001879 gelation Methods 0.000 description 1
- 239000010438 granite Substances 0.000 description 1
- 125000001475 halogen functional group Chemical group 0.000 description 1
- 150000003944 halohydrins Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 150000002432 hydroperoxides Chemical class 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 150000003949 imides Chemical class 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 231100000518 lethal Toxicity 0.000 description 1
- 230000001665 lethal effect Effects 0.000 description 1
- 230000004060 metabolic process Effects 0.000 description 1
- 150000002734 metacrylic acid derivatives Chemical class 0.000 description 1
- 150000001247 metal acetylides Chemical class 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 239000002923 metal particle Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 125000005395 methacrylic acid group Chemical class 0.000 description 1
- XBDAKYZJVVYINU-UHFFFAOYSA-N methyl 2-methylprop-2-enoate;2-(2-methylprop-2-enoyloxy)ethyl 2-methylprop-2-enoate Chemical compound COC(=O)C(C)=C.CC(=C)C(=O)OCCOC(=O)C(C)=C XBDAKYZJVVYINU-UHFFFAOYSA-N 0.000 description 1
- 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
- 150000002825 nitriles Chemical class 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
- 150000007524 organic acids Chemical class 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- CZYFDZPOVORIRJ-UHFFFAOYSA-N oxiran-2-amine Chemical compound NC1CO1 CZYFDZPOVORIRJ-UHFFFAOYSA-N 0.000 description 1
- 238000001935 peptisation Methods 0.000 description 1
- 150000004978 peroxycarbonates Chemical class 0.000 description 1
- 125000005634 peroxydicarbonate group Chemical group 0.000 description 1
- 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
- LTEKQAPRXFBRNN-UHFFFAOYSA-N piperidin-4-ylmethanamine Chemical compound NCC1CCNCC1 LTEKQAPRXFBRNN-UHFFFAOYSA-N 0.000 description 1
- 229920002587 poly(1,3-butadiene) polymer Polymers 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
- 238000003825 pressing Methods 0.000 description 1
- GUYXXEXGKVKXAW-UHFFFAOYSA-N prop-2-enenitrile Chemical compound C=CC#N.C=CC#N GUYXXEXGKVKXAW-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
- 238000005086 pumping Methods 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 239000012265 solid product Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 229920006132 styrene block copolymer Polymers 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 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
- 238000010998 test method Methods 0.000 description 1
- 238000002076 thermal analysis method Methods 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
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 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)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Polymerisation Methods In General (AREA)
- Dental Preparations (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
- Pigments, Carbon Blacks, Or Wood Stains (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB919124305A GB9124305D0 (en) | 1991-11-15 | 1991-11-15 | Polymerisable compositions |
| GB919124307A GB9124307D0 (en) | 1991-11-15 | 1991-11-15 | Polymeric dispersants and filled compositions containing them |
| GB919124309A GB9124309D0 (en) | 1991-11-15 | 1991-11-15 | Polymerisable compositions |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SI9200321A true SI9200321A (en) | 1993-06-30 |
Family
ID=27265926
Family Applications (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SI19929200321A SI9200321A (en) | 1991-11-15 | 1992-11-13 | Filled cured compositions for the preparation of thermoplastic products |
| SI9200320A SI9200320B (en) | 1991-11-15 | 1992-11-13 | Filled cured compositions for the preparation of thermoplastic products |
| SI19929200319A SI9200319A (en) | 1991-11-15 | 1992-11-13 | Polymeric dispersants and filled compositions containing them |
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 |
| SI19929200319A SI9200319A (en) | 1991-11-15 | 1992-11-13 | Polymeric dispersants and filled compositions containing them |
Country Status (16)
| Country | Link |
|---|---|
| US (3) | US5519083A (el) |
| EP (3) | EP0612334B1 (el) |
| JP (3) | JPH07501097A (el) |
| AT (3) | ATE147082T1 (el) |
| AU (3) | AU668369B2 (el) |
| CA (3) | CA2121468A1 (el) |
| DE (3) | DE69216427T2 (el) |
| DK (1) | DK0612328T3 (el) |
| ES (3) | ES2096108T3 (el) |
| GB (3) | GB9223629D0 (el) |
| GR (3) | GR3022214T3 (el) |
| NZ (3) | NZ245120A (el) |
| PT (3) | PT101056B (el) |
| SI (3) | SI9200321A (el) |
| TW (3) | TW224482B (el) |
| WO (3) | WO1993010182A1 (el) |
Families Citing this family (30)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU668369B2 (en) * | 1991-11-15 | 1996-05-02 | Imperial Chemical Industries Plc | Polymerisable compositions |
| TW321658B (el) * | 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 |
| DE69531545T2 (de) * | 1994-06-23 | 2004-06-24 | Affymax Technologies N.V., Willemstad | Photolabile verbindungen und verfahren für deren verwendung |
| 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 |
| DE60219934T2 (de) * | 2001-09-25 | 2008-01-17 | 3M Innovative Properties Co., St. Paul | Härtbare dispergiermittel |
| 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 |
| 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 |
| 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 |
| 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 |
| EP2511062A1 (en) * | 2008-11-20 | 2012-10-17 | Allergan, Inc. | System and method for molding soft fluid-filled implant shells |
| 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 |
| JP7046542B2 (ja) * | 2016-09-29 | 2022-04-04 | 日東電工株式会社 | 構造物上の塗膜、塗膜を形成するための塗料セット及び下塗層用塗料並びに塗工方法 |
| 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 |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| 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 |
| GB8713693D0 (en) * | 1987-06-11 | 1987-07-15 | Ici Plc | Fillers |
| 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 |
| FR2682396B1 (fr) * | 1991-10-09 | 1995-01-06 | Pasteur Institut | Sequence nucleique du gene associe au syndrome de kallmann lie au chromosome x, sequences peptidiques correspondantes; applications diagnostiques. |
| AU668369B2 (en) * | 1991-11-15 | 1996-05-02 | Imperial Chemical Industries Plc | Polymerisable compositions |
| US5283288A (en) * | 1992-01-07 | 1994-02-01 | Ciba Corning Diagnostics Corp. | PVC coatings for electrodes |
-
1992
- 1992-11-11 AU AU29065/92A patent/AU668369B2/en not_active Ceased
- 1992-11-11 GB GB929223629A patent/GB9223629D0/en active Pending
- 1992-11-11 WO PCT/GB1992/002080 patent/WO1993010182A1/en not_active Ceased
- 1992-11-11 AT AT92922920T patent/ATE147082T1/de active
- 1992-11-11 DK DK92922920.1T patent/DK0612328T3/da active
- 1992-11-11 ES ES92922920T patent/ES2096108T3/es not_active Expired - Lifetime
- 1992-11-11 JP JP50906693A patent/JPH07501097A/ja active Pending
- 1992-11-11 WO PCT/GB1992/002081 patent/WO1993010183A1/en not_active Ceased
- 1992-11-11 WO PCT/GB1992/002079 patent/WO1993010159A1/en not_active Ceased
- 1992-11-11 AT AT92923015T patent/ATE188980T1/de not_active IP Right Cessation
- 1992-11-11 JP JP05509068A patent/JP3133334B2/ja not_active Expired - Fee Related
- 1992-11-11 AT AT92922894T patent/ATE198615T1/de active
- 1992-11-11 EP EP92923015A patent/EP0612334B1/en not_active Expired - Lifetime
- 1992-11-11 AU AU29032/92A patent/AU665380B2/en not_active Ceased
- 1992-11-11 CA CA002121468A patent/CA2121468A1/en not_active Abandoned
- 1992-11-11 GB GB929223628A patent/GB9223628D0/en active Pending
- 1992-11-11 ES ES92923015T patent/ES2141113T3/es not_active Expired - Lifetime
- 1992-11-11 CA CA002123429A patent/CA2123429C/en not_active Expired - Lifetime
- 1992-11-11 DE DE69216427T patent/DE69216427T2/de not_active Expired - Lifetime
- 1992-11-11 ES ES92922894T patent/ES2155063T3/es not_active Expired - Lifetime
- 1992-11-11 DE DE69230587T patent/DE69230587T2/de not_active Expired - Fee Related
- 1992-11-11 DE DE69231635T patent/DE69231635T2/de not_active Expired - Lifetime
- 1992-11-11 EP EP92922920A patent/EP0612328B1/en not_active Expired - Lifetime
- 1992-11-11 GB GB929223602A patent/GB9223602D0/en active Pending
- 1992-11-11 JP JP5509067A patent/JPH07501098A/ja active Pending
- 1992-11-11 AU AU29053/92A patent/AU657180B2/en not_active Ceased
- 1992-11-11 US US08/204,181 patent/US5519083A/en not_active Expired - Lifetime
- 1992-11-11 CA CA002121469A patent/CA2121469C/en not_active Expired - Lifetime
- 1992-11-11 EP EP92922894A patent/EP0612333B1/en not_active Expired - Lifetime
- 1992-11-11 US US08/244,264 patent/US5530064A/en not_active Expired - Lifetime
- 1992-11-13 PT PT101056A patent/PT101056B/pt not_active IP Right Cessation
- 1992-11-13 PT PT101054A patent/PT101054B/pt not_active IP Right Cessation
- 1992-11-13 NZ NZ245120A patent/NZ245120A/en unknown
- 1992-11-13 SI SI19929200321A patent/SI9200321A/sl unknown
- 1992-11-13 SI SI9200320A patent/SI9200320B/sl unknown
- 1992-11-13 SI SI19929200319A patent/SI9200319A/sl unknown
- 1992-11-13 NZ NZ245121A patent/NZ245121A/en unknown
- 1992-11-13 NZ NZ245122A patent/NZ245122A/en unknown
- 1992-11-13 PT PT101055A patent/PT101055B/pt not_active IP Right Cessation
- 1992-12-18 TW TW081110208A patent/TW224482B/zh not_active IP Right Cessation
- 1992-12-18 TW TW081110186A patent/TW226390B/zh not_active IP Right Cessation
- 1992-12-18 TW TW081110199A patent/TW270135B/zh active
-
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
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