NO311225B1 - Epoksypolysiloksanpolymerblanding og fremgangsmåte for fremstilling derav - Google Patents

Epoksypolysiloksanpolymerblanding og fremgangsmåte for fremstilling derav Download PDF

Info

Publication number: NO311225B1
Authority: NO; Norway
Prior art keywords: polysiloxane; epoxy; group; mixture; epoxy resin
Prior art date: 1997-01-27

Application number

NO19993629A

Other languages

English (en)

Norwegian (no)

Other versions

NO993629D0 (no

NO993629L (no

Inventor

Norman R Mowrer

Raymond E Foscante

J Luis Rojas

Original Assignee

Ameron Int Corp

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.)

1997-01-27

Filing date

1999-07-26

Publication date

2001-10-29

1999-07-26 Application filed by Ameron Int Corp filed Critical Ameron Int Corp

1999-07-26 Publication of NO993629D0 publication Critical patent/NO993629D0/no

1999-09-27 Publication of NO993629L publication Critical patent/NO993629L/no

2001-10-29 Publication of NO311225B1 publication Critical patent/NO311225B1/no

Links

-1 Polysiloxane Polymers 0.000 title claims description 171
229920001296 polysiloxane Polymers 0.000 title claims description 157
239000004593 Epoxy Substances 0.000 title claims description 101
229920002959 polymer blend Polymers 0.000 title claims description 18
238000000034 method Methods 0.000 title claims description 7
238000002360 preparation method Methods 0.000 title description 2
239000000203 mixture Substances 0.000 claims description 107
239000003822 epoxy resin Substances 0.000 claims description 76
229920000647 polyepoxide Polymers 0.000 claims description 76
229920000642 polymer Polymers 0.000 claims description 63
125000003118 aryl group Chemical group 0.000 claims description 42
FZHAPNGMFPVSLP-UHFFFAOYSA-N silanamine Chemical compound [SiH3]N FZHAPNGMFPVSLP-UHFFFAOYSA-N 0.000 claims description 42
239000000049 pigment Substances 0.000 claims description 35
229920005989 resin Polymers 0.000 claims description 30
239000011347 resin Substances 0.000 claims description 30
125000000217 alkyl group Chemical group 0.000 claims description 29
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 28
239000004848 polyfunctional curative Substances 0.000 claims description 26
125000004432 carbon atom Chemical group C* 0.000 claims description 25
150000001412 amines Chemical class 0.000 claims description 20
239000000463 material Substances 0.000 claims description 19
239000003795 chemical substances by application Substances 0.000 claims description 17
239000003054 catalyst Substances 0.000 claims description 16
239000004606 Fillers/Extenders Substances 0.000 claims description 11
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 11
125000004183 alkoxy alkyl group Chemical group 0.000 claims description 9
125000003545 alkoxy group Chemical group 0.000 claims description 9
238000006460 hydrolysis reaction Methods 0.000 claims description 9
239000013008 thixotropic agent Substances 0.000 claims description 9
239000002518 antifoaming agent Substances 0.000 claims description 8
150000002118 epoxides Chemical group 0.000 claims description 8
229910052739 hydrogen Inorganic materials 0.000 claims description 8
239000001257 hydrogen Substances 0.000 claims description 8
230000007062 hydrolysis Effects 0.000 claims description 8
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 8
125000002768 hydroxyalkyl group Chemical group 0.000 claims description 8
230000015572 biosynthetic process Effects 0.000 claims description 7
239000010419 fine particle Substances 0.000 claims description 7
238000004519 manufacturing process Methods 0.000 claims description 7
239000000080 wetting agent Substances 0.000 claims description 7
CNPURSDMOWDNOQ-UHFFFAOYSA-N 4-methoxy-7h-pyrrolo[2,3-d]pyrimidin-2-amine Chemical compound COC1=NC(N)=NC2=C1C=CN2 CNPURSDMOWDNOQ-UHFFFAOYSA-N 0.000 claims description 6
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 6
238000006243 chemical reaction Methods 0.000 claims description 6
125000000753 cycloalkyl group Chemical group 0.000 claims description 6
239000004014 plasticizer Substances 0.000 claims description 6
238000006068 polycondensation reaction Methods 0.000 claims description 6
239000006254 rheological additive Substances 0.000 claims description 6
BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical group [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims description 5
239000013036 UV Light Stabilizer Substances 0.000 claims description 5
239000010426 asphalt Substances 0.000 claims description 5
IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical class C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 claims description 5
125000003700 epoxy group Chemical group 0.000 claims description 5
150000001875 compounds Chemical class 0.000 claims description 4
239000003085 diluting agent Substances 0.000 claims description 4
239000006185 dispersion Substances 0.000 claims description 4
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 3
239000000654 additive Substances 0.000 claims description 3
125000003277 amino group Chemical group 0.000 claims description 3
GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical class C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 claims description 3
229910052742 iron Inorganic materials 0.000 claims description 3
239000003607 modifier Substances 0.000 claims description 3
229920001187 thermosetting polymer Polymers 0.000 claims description 3
ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims description 2
RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 2
QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 claims description 2
239000003570 air Substances 0.000 claims description 2
239000010941 cobalt Substances 0.000 claims description 2
229910017052 cobalt Inorganic materials 0.000 claims description 2
GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 2
239000011133 lead Substances 0.000 claims description 2
WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 claims description 2
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239000002184 metal Substances 0.000 claims description 2
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239000010936 titanium Substances 0.000 claims description 2
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239000011701 zinc Substances 0.000 claims description 2
229910052725 zinc Inorganic materials 0.000 claims description 2
229910052726 zirconium Inorganic materials 0.000 claims description 2
ORLQHILJRHBSAY-UHFFFAOYSA-N [1-(hydroxymethyl)cyclohexyl]methanol Chemical class OCC1(CO)CCCCC1 ORLQHILJRHBSAY-UHFFFAOYSA-N 0.000 claims 2
239000004841 bisphenol A epoxy resin Substances 0.000 claims 2
239000011353 cycloaliphatic epoxy resin Substances 0.000 claims 2
238000001556 precipitation Methods 0.000 claims 1
239000000306 component Substances 0.000 description 58
238000000576 coating method Methods 0.000 description 33
239000000126 substance Substances 0.000 description 29
239000011248 coating agent Substances 0.000 description 25
238000005260 corrosion Methods 0.000 description 15
230000007797 corrosion Effects 0.000 description 15
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GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 11
239000002904 solvent Substances 0.000 description 11
LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 8
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230000009257 reactivity Effects 0.000 description 7
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244000007853 Sarothamnus scoparius Species 0.000 description 3
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
150000001298 alcohols Chemical class 0.000 description 3
125000001931 aliphatic group Chemical group 0.000 description 3
229910052782 aluminium Inorganic materials 0.000 description 3
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
238000000889 atomisation Methods 0.000 description 3
230000015556 catabolic process Effects 0.000 description 3
239000003153 chemical reaction reagent Substances 0.000 description 3
230000000052 comparative effect Effects 0.000 description 3
238000006731 degradation reaction Methods 0.000 description 3
239000003960 organic solvent Substances 0.000 description 3
238000006116 polymerization reaction Methods 0.000 description 3
150000003254 radicals Chemical class 0.000 description 3
239000000758 substrate Substances 0.000 description 3
WYTZZXDRDKSJID-UHFFFAOYSA-N (3-aminopropyl)triethoxysilane Chemical compound CCO[Si](OCC)(OCC)CCCN WYTZZXDRDKSJID-UHFFFAOYSA-N 0.000 description 2
KUBDPQJOLOUJRM-UHFFFAOYSA-N 2-(chloromethyl)oxirane;4-[2-(4-hydroxyphenyl)propan-2-yl]phenol Chemical class ClCC1CO1.C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 KUBDPQJOLOUJRM-UHFFFAOYSA-N 0.000 description 2
SJECZPVISLOESU-UHFFFAOYSA-N 3-trimethoxysilylpropan-1-amine Chemical compound CO[Si](OC)(OC)CCCN SJECZPVISLOESU-UHFFFAOYSA-N 0.000 description 2
229920000178 Acrylic resin Polymers 0.000 description 2
239000004925 Acrylic resin Substances 0.000 description 2
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
240000004160 Capsicum annuum Species 0.000 description 2
235000008534 Capsicum annuum var annuum Nutrition 0.000 description 2
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 2
238000005299 abrasion Methods 0.000 description 2
239000004411 aluminium Substances 0.000 description 2
TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
230000033228 biological regulation Effects 0.000 description 2
230000001010 compromised effect Effects 0.000 description 2
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238000004132 cross linking Methods 0.000 description 2
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WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical compound CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 description 2
238000005096 rolling process Methods 0.000 description 2
150000003839 salts Chemical class 0.000 description 2
229910000077 silane Inorganic materials 0.000 description 2
238000010998 test method Methods 0.000 description 2
XGIKILRODBEJIL-UHFFFAOYSA-N 1-(ethylamino)ethanol Chemical compound CCNC(C)O XGIKILRODBEJIL-UHFFFAOYSA-N 0.000 description 1
OSNILPMOSNGHLC-UHFFFAOYSA-N 1-[4-methoxy-3-(piperidin-1-ylmethyl)phenyl]ethanone Chemical compound COC1=CC=C(C(C)=O)C=C1CN1CCCCC1 OSNILPMOSNGHLC-UHFFFAOYSA-N 0.000 description 1
MFYSUUPKMDJYPF-UHFFFAOYSA-N 2-[(4-methyl-2-nitrophenyl)diazenyl]-3-oxo-n-phenylbutanamide Chemical compound C=1C=CC=CC=1NC(=O)C(C(=O)C)N=NC1=CC=C(C)C=C1[N+]([O-])=O MFYSUUPKMDJYPF-UHFFFAOYSA-N 0.000 description 1
HIGURUTWFKYJCH-UHFFFAOYSA-N 2-[[1-(oxiran-2-ylmethoxymethyl)cyclohexyl]methoxymethyl]oxirane Chemical compound C1OC1COCC1(COCC2OC2)CCCCC1 HIGURUTWFKYJCH-UHFFFAOYSA-N 0.000 description 1
HUPGCAGBHBJUJC-UHFFFAOYSA-N 3-(3-trimethoxysilylpropoxy)aniline Chemical compound CO[Si](OC)(OC)CCCOC1=CC=CC(N)=C1 HUPGCAGBHBJUJC-UHFFFAOYSA-N 0.000 description 1
RREANTFLPGEWEN-MBLPBCRHSA-N 7-[4-[[(3z)-3-[4-amino-5-[(3,4,5-trimethoxyphenyl)methyl]pyrimidin-2-yl]imino-5-fluoro-2-oxoindol-1-yl]methyl]piperazin-1-yl]-1-cyclopropyl-6-fluoro-4-oxoquinoline-3-carboxylic acid Chemical compound COC1=C(OC)C(OC)=CC(CC=2C(=NC(\N=C/3C4=CC(F)=CC=C4N(CN4CCN(CC4)C=4C(=CC=5C(=O)C(C(O)=O)=CN(C=5C=4)C4CC4)F)C\3=O)=NC=2)N)=C1 RREANTFLPGEWEN-MBLPBCRHSA-N 0.000 description 1
CGLVZFOCZLHKOH-UHFFFAOYSA-N 8,18-dichloro-5,15-diethyl-5,15-dihydrodiindolo(3,2-b:3',2'-m)triphenodioxazine Chemical compound CCN1C2=CC=CC=C2C2=C1C=C1OC3=C(Cl)C4=NC(C=C5C6=CC=CC=C6N(C5=C5)CC)=C5OC4=C(Cl)C3=NC1=C2 CGLVZFOCZLHKOH-UHFFFAOYSA-N 0.000 description 1
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239000001692 EU approved anti-caking agent Substances 0.000 description 1
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GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
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ISKQADXMHQSTHK-UHFFFAOYSA-N [4-(aminomethyl)phenyl]methanamine Chemical compound NCC1=CC=C(CN)C=C1 ISKQADXMHQSTHK-UHFFFAOYSA-N 0.000 description 1
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238000007086 side reaction Methods 0.000 description 1
150000004756 silanes Chemical class 0.000 description 1
150000004819 silanols Chemical class 0.000 description 1
235000012239 silicon dioxide Nutrition 0.000 description 1
239000001632 sodium acetate Substances 0.000 description 1
235000017281 sodium acetate Nutrition 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000000600 sorbitol Substances 0.000 description 1
229910052717 sulfur Inorganic materials 0.000 description 1
239000011593 sulfur Substances 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
239000000375 suspending agent Substances 0.000 description 1
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
229920002554 vinyl polymer Polymers 0.000 description 1
238000004065 wastewater treatment Methods 0.000 description 1
230000002087 whitening effect Effects 0.000 description 1
239000002023 wood Substances 0.000 description 1
239000008096 xylene Substances 0.000 description 1
239000011787 zinc oxide Substances 0.000 description 1

Classifications

- 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
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/40—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the curing agents used
- C08G59/4007—Curing agents not provided for by the groups C08G59/42 - C08G59/66
- C08G59/4085—Curing agents not provided for by the groups C08G59/42 - C08G59/66 silicon containing compounds
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L63/00—Compositions of epoxy resins; Compositions of derivatives of epoxy resins
- 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
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D163/00—Coating compositions based on epoxy resins; Coating compositions based on derivatives of epoxy resins
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D183/00—Coating compositions based on 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; Coating compositions based on derivatives of such polymers
- C09D183/04—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
- C08G77/04—Polysiloxanes
- C08G77/12—Polysiloxanes containing silicon bound to hydrogen
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/04—Polysiloxanes
- C08G77/14—Polysiloxanes containing silicon bound to oxygen-containing groups
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/04—Polysiloxanes
- C08G77/14—Polysiloxanes containing silicon bound to oxygen-containing groups
- C08G77/16—Polysiloxanes containing silicon bound to oxygen-containing groups to hydroxyl groups
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/04—Polysiloxanes
- C08G77/14—Polysiloxanes containing silicon bound to oxygen-containing groups
- C08G77/18—Polysiloxanes containing silicon bound to oxygen-containing groups to alkoxy or aryloxy groups
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/04—Polysiloxanes
- C08G77/22—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen
- C08G77/26—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen nitrogen-containing groups
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/42—Block-or graft-polymers containing polysiloxane sequences
- C08G77/46—Block-or graft-polymers containing polysiloxane sequences containing polyether sequences
- 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
- C08G77/70—Siloxanes defined by use of the MDTQ nomenclature

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Chemical Kinetics & Catalysis (AREA)
Health & Medical Sciences (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Life Sciences & Earth Sciences (AREA)
Engineering & Computer Science (AREA)
Materials Engineering (AREA)
Wood Science & Technology (AREA)
Paints Or Removers (AREA)
Epoxy Resins (AREA)
Compositions Of Macromolecular Compounds (AREA)
Other Resins Obtained By Reactions Not Involving Carbon-To-Carbon Unsaturated Bonds (AREA)
Silicon Polymers (AREA)

NO19993629A 1997-01-27 1999-07-26 Epoksypolysiloksanpolymerblanding og fremgangsmåte for fremstilling derav NO311225B1 (no)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US08/790,730 US5804616A (en)	1993-05-19	1997-01-27	Epoxy-polysiloxane polymer composition
PCT/US1997/007594 WO1998032792A1 (en)	1997-01-27	1997-05-06	Epoxy-polysiloxane polymer composition

Publications (3)

Publication Number	Publication Date
NO993629D0 NO993629D0 (no)	1999-07-26
NO993629L NO993629L (no)	1999-09-27
NO311225B1 true NO311225B1 (no)	2001-10-29

Family

ID=25151596

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO19993629A NO311225B1 (no)	1997-01-27	1999-07-26	Epoksypolysiloksanpolymerblanding og fremgangsmåte for fremstilling derav

Country Status (27)

Country	Link
US (1)	US5804616A (da)
EP (2)	EP1849831B1 (da)
JP (3)	JP4194662B2 (da)
KR (1)	KR100615959B1 (da)
CN (1)	CN100500745C (da)
AR (1)	AR008000A1 (da)
AT (2)	ATE454422T1 (da)
AU (2)	AU2932997A (da)
BR (1)	BR9714295A (da)
CA (1)	CA2279516C (da)
CO (1)	CO4890878A1 (da)
CZ (1)	CZ300637B6 (da)
DE (2)	DE69738238T2 (da)
DK (2)	DK0954547T3 (da)
ES (2)	ES2338377T3 (da)
HU (1)	HU224481B1 (da)
ID (1)	ID19758A (da)
IL (1)	IL131019A (da)
MY (1)	MY131828A (da)
NO (1)	NO311225B1 (da)
NZ (1)	NZ336844A (da)
PL (1)	PL191008B1 (da)
PT (2)	PT1849831E (da)
RU (1)	RU2195471C2 (da)
TR (1)	TR199902369T2 (da)
TW (1)	TW469287B (da)
WO (1)	WO1998032792A1 (da)

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1997
- 1997-01-27 US US08/790,730 patent/US5804616A/en not_active Expired - Lifetime
- 1997-05-06 WO PCT/US1997/007594 patent/WO1998032792A1/en active IP Right Grant
- 1997-05-06 HU HU0000660A patent/HU224481B1/hu not_active IP Right Cessation
- 1997-05-06 ES ES07114112T patent/ES2338377T3/es not_active Expired - Lifetime
- 1997-05-06 PL PL334799A patent/PL191008B1/pl unknown
- 1997-05-06 DE DE69738238T patent/DE69738238T2/de not_active Expired - Lifetime
- 1997-05-06 IL IL13101997A patent/IL131019A/en not_active IP Right Cessation
- 1997-05-06 TR TR1999/02369T patent/TR199902369T2/xx unknown
- 1997-05-06 AT AT07114112T patent/ATE454422T1/de not_active IP Right Cessation
- 1997-05-06 DK DK97923555T patent/DK0954547T3/da active
- 1997-05-06 RU RU99118515/04A patent/RU2195471C2/ru not_active IP Right Cessation
- 1997-05-06 JP JP53194498A patent/JP4194662B2/ja not_active Expired - Lifetime
- 1997-05-06 AU AU29329/97A patent/AU2932997A/en not_active Abandoned
- 1997-05-06 KR KR1019997006776A patent/KR100615959B1/ko not_active IP Right Cessation
- 1997-05-06 EP EP07114112A patent/EP1849831B1/en not_active Expired - Lifetime
- 1997-05-06 CN CNB971819580A patent/CN100500745C/zh not_active Expired - Lifetime
- 1997-05-06 CA CA002279516A patent/CA2279516C/en not_active Expired - Lifetime
- 1997-05-06 DE DE69739738T patent/DE69739738D1/de not_active Expired - Lifetime
- 1997-05-06 BR BR9714295-6A patent/BR9714295A/pt not_active IP Right Cessation
- 1997-05-06 CZ CZ0263599A patent/CZ300637B6/cs not_active IP Right Cessation
- 1997-05-06 ES ES97923555T patent/ES2292186T3/es not_active Expired - Lifetime
- 1997-05-06 AT AT97923555T patent/ATE376568T1/de not_active IP Right Cessation
- 1997-05-06 EP EP97923555A patent/EP0954547B1/en not_active Expired - Lifetime
- 1997-05-06 NZ NZ336844A patent/NZ336844A/xx not_active IP Right Cessation
- 1997-05-06 DK DK07114112.1T patent/DK1849831T3/da active
- 1997-05-06 PT PT07114112T patent/PT1849831E/pt unknown
- 1997-05-06 PT PT97923555T patent/PT954547E/pt unknown
- 1997-07-01 AU AU28429/97A patent/AU726606B2/en not_active Expired
- 1997-07-15 MY MYPI97003198A patent/MY131828A/en unknown
- 1997-07-25 AR ARP970103381A patent/AR008000A1/es active IP Right Grant
- 1997-08-15 CO CO97047262A patent/CO4890878A1/es unknown
- 1997-10-04 TW TW086114525A patent/TW469287B/zh not_active IP Right Cessation
- 1997-10-06 ID IDP973362A patent/ID19758A/id unknown
1999
- 1999-07-26 NO NO19993629A patent/NO311225B1/no not_active IP Right Cessation
2007
- 2007-08-03 JP JP2007203687A patent/JP2007314800A/ja not_active Withdrawn
2011
- 2011-03-28 JP JP2011070815A patent/JP5361084B2/ja not_active Expired - Lifetime

Also Published As

Publication number	Publication date
AR008000A1 (es)	1999-11-24
DE69738238D1 (de)	2007-12-06
ES2338377T3 (es)	2010-05-06
PL334799A1 (en)	2000-03-13
CN1247547A (zh)	2000-03-15
EP0954547A4 (en)	2000-03-29
ES2292186T3 (es)	2008-03-01
WO1998032792A1 (en)	1998-07-30
TW469287B (en)	2001-12-21
JP2011157558A (ja)	2011-08-18
PL191008B1 (pl)	2006-03-31
AU2932997A (en)	1998-08-18
DK0954547T3 (da)	2008-01-28
PT954547E (pt)	2007-11-08
RU2195471C2 (ru)	2002-12-27
HUP0000660A2 (en)	2000-07-28
ATE376568T1 (de)	2007-11-15
JP4194662B2 (ja)	2008-12-10
KR20000070531A (ko)	2000-11-25
CZ300637B6 (cs)	2009-07-08
DE69739738D1 (de)	2010-02-25
AU2842997A (en)	1999-01-14
ID19758A (id)	1998-07-30
IL131019A0 (en)	2001-01-28
JP5361084B2 (ja)	2013-12-04
CN100500745C (zh)	2009-06-17
TR199902369T2 (xx)	2000-04-21
IL131019A (en)	2004-12-15
DE69738238T2 (de)	2008-07-31
CZ9902635A3 (cs)	2000-12-13
CA2279516C (en)	2005-03-15
HU224481B1 (hu)	2005-09-28
ATE454422T1 (de)	2010-01-15
JP2007314800A (ja)	2007-12-06
EP0954547B1 (en)	2007-10-24
US5804616A (en)	1998-09-08
KR100615959B1 (ko)	2006-08-28
NZ336844A (en)	2000-01-28
PT1849831E (pt)	2010-02-03
EP0954547A1 (en)	1999-11-10
NO993629D0 (no)	1999-07-26
CO4890878A1 (es)	2000-02-28
NO993629L (no)	1999-09-27
AU726606B2 (en)	2000-11-16
EP1849831A3 (en)	2008-01-23
EP1849831A2 (en)	2007-10-31
JP2001509188A (ja)	2001-07-10
EP1849831B1 (en)	2010-01-06
HUP0000660A3 (en)	2000-11-28
DK1849831T3 (da)	2010-03-08
CA2279516A1 (en)	1998-07-30
MY131828A (en)	2007-09-28
BR9714295A (pt)	2000-04-25

Publication	Publication Date	Title
NO311225B1 (no)	2001-10-29	Epoksypolysiloksanpolymerblanding og fremgangsmåte for fremstilling derav
KR100376362B1 (ko)	2003-07-18	에폭시폴리실록산폴리머코팅조성물및그제조방법
KR102128213B1 (ko)	2020-06-29	에폭시 실록산 코팅 조성물
CN105073919B (zh)	2017-09-29	环氧硅氧烷涂料组合物
MXPA99006925A (en)	2000-02-02	Epoxy-polysiloxane polymer composition

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