CA2073155A1 - Composition de vulcanisation double et utilisation de celle-ci - Google Patents

Composition de vulcanisation double et utilisation de celle-ci

Info

Publication number: CA2073155A1
Authority: CA; Canada
Prior art keywords: coating; adduct; composition; composition according; free
Prior art date: 1991-07-16
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Abandoned

Application number

CA 2073155

Other languages

English (en)

Inventor

David R. Kyle

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

National Starch and Chemical Investment Holding Corp

Original Assignee

Individual

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.)

1991-07-16

Filing date

1992-07-06

Publication date

1993-01-17

1992-07-06 Application filed by Individual filed Critical Individual

1993-01-17 Publication of CA2073155A1 publication Critical patent/CA2073155A1/fr

Status Abandoned legal-status Critical Current

Links

239000000203 mixture Substances 0.000 title claims abstract description 69
230000009977 dual effect Effects 0.000 title claims abstract description 21
238000000576 coating method Methods 0.000 claims abstract description 59
239000011248 coating agent Substances 0.000 claims abstract description 40
NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims abstract description 26
239000012948 isocyanate Substances 0.000 claims abstract description 25
150000002513 isocyanates Chemical class 0.000 claims abstract description 15
239000003085 diluting agent Substances 0.000 claims abstract description 12
IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims abstract description 12
125000000524 functional group Chemical group 0.000 claims abstract description 7
-1 aliphatic isocyanate Chemical class 0.000 claims description 19
238000000034 method Methods 0.000 claims description 14
239000013638 trimer Substances 0.000 claims description 8
RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 claims description 7
239000005057 Hexamethylene diisocyanate Substances 0.000 claims description 6
230000005855 radiation Effects 0.000 claims description 6
239000008199 coating composition Substances 0.000 claims description 5
238000004382 potting Methods 0.000 claims description 5
239000000047 product Substances 0.000 claims description 5
125000002768 hydroxyalkyl group Chemical group 0.000 claims description 4
ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical group OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 claims description 3
238000005829 trimerization reaction Methods 0.000 claims description 3
239000007795 chemical reaction product Substances 0.000 claims description 2
238000001723 curing Methods 0.000 description 26
239000005056 polyisocyanate Substances 0.000 description 23
229920001228 polyisocyanate Polymers 0.000 description 23
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 12
238000006243 chemical reaction Methods 0.000 description 12
239000004094 surface-active agent Substances 0.000 description 11
239000000178 monomer Substances 0.000 description 10
238000012360 testing method Methods 0.000 description 10
OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 7
230000007246 mechanism Effects 0.000 description 7
150000001875 compounds Chemical class 0.000 description 6
239000000356 contaminant Substances 0.000 description 6
125000002887 hydroxy group Chemical group [H]O* 0.000 description 6
229910052751 metal Inorganic materials 0.000 description 6
239000002184 metal Substances 0.000 description 6
NWVVVBRKAWDGAB-UHFFFAOYSA-N p-methoxyphenol Chemical compound COC1=CC=C(O)C=C1 NWVVVBRKAWDGAB-UHFFFAOYSA-N 0.000 description 6
125000003118 aryl group Chemical group 0.000 description 5
238000004132 cross linking Methods 0.000 description 5
238000009472 formulation Methods 0.000 description 5
230000003301 hydrolyzing effect Effects 0.000 description 5
238000009413 insulation Methods 0.000 description 5
238000003860 storage Methods 0.000 description 5
239000004594 Masterbatch (MB) Substances 0.000 description 4
239000000853 adhesive Substances 0.000 description 4
230000001070 adhesive effect Effects 0.000 description 4
125000000217 alkyl group Chemical group 0.000 description 4
WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 4
239000003112 inhibitor Substances 0.000 description 4
239000007788 liquid Substances 0.000 description 4
238000013008 moisture curing Methods 0.000 description 4
HVLLSGMXQDNUAL-UHFFFAOYSA-N triphenyl phosphite Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)OC1=CC=CC=C1 HVLLSGMXQDNUAL-UHFFFAOYSA-N 0.000 description 4
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
LVGFPWDANALGOY-UHFFFAOYSA-N 8-methylnonyl prop-2-enoate Chemical compound CC(C)CCCCCCCOC(=O)C=C LVGFPWDANALGOY-UHFFFAOYSA-N 0.000 description 3
239000005058 Isophorone diisocyanate Substances 0.000 description 3
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 3
150000001252 acrylic acid derivatives Chemical class 0.000 description 3
125000001931 aliphatic group Chemical group 0.000 description 3
230000015556 catabolic process Effects 0.000 description 3
239000003054 catalyst Substances 0.000 description 3
239000012975 dibutyltin dilaurate Substances 0.000 description 3
150000002009 diols Chemical class 0.000 description 3
239000011521 glass Substances 0.000 description 3
NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 3
238000002156 mixing Methods 0.000 description 3
239000002904 solvent Substances 0.000 description 3
RZVINYQDSSQUKO-UHFFFAOYSA-N 2-phenoxyethyl prop-2-enoate Chemical compound C=CC(=O)OCCOC1=CC=CC=C1 RZVINYQDSSQUKO-UHFFFAOYSA-N 0.000 description 2
UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 2
GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 2
XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical compound ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 2
239000000654 additive Substances 0.000 description 2
239000002318 adhesion promoter Substances 0.000 description 2
230000002411 adverse Effects 0.000 description 2
125000002877 alkyl aryl group Chemical group 0.000 description 2
125000000746 allylic group Chemical group 0.000 description 2
125000004429 atom Chemical group 0.000 description 2
230000008901 benefit Effects 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
OHJMTUPIZMNBFR-UHFFFAOYSA-N biuret Chemical compound NC(=O)NC(N)=O OHJMTUPIZMNBFR-UHFFFAOYSA-N 0.000 description 2
125000004432 carbon atom Chemical group C* 0.000 description 2
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 2
239000002738 chelating agent Substances 0.000 description 2
239000004020 conductor Substances 0.000 description 2
239000003431 cross linking reagent Substances 0.000 description 2
238000006731 degradation reaction Methods 0.000 description 2
UHESRSKEBRADOO-UHFFFAOYSA-N ethyl carbamate;prop-2-enoic acid Chemical compound OC(=O)C=C.CCOC(N)=O UHESRSKEBRADOO-UHFFFAOYSA-N 0.000 description 2
230000004907 flux Effects 0.000 description 2
238000007654 immersion Methods 0.000 description 2
239000003999 initiator Substances 0.000 description 2
238000004519 manufacturing process Methods 0.000 description 2
239000000463 material Substances 0.000 description 2
239000002808 molecular sieve Substances 0.000 description 2
239000004033 plastic Substances 0.000 description 2
229920003023 plastic Polymers 0.000 description 2
229920000728 polyester Polymers 0.000 description 2
229920000570 polyether Polymers 0.000 description 2
230000001681 protective effect Effects 0.000 description 2
239000011541 reaction mixture Substances 0.000 description 2
230000035939 shock Effects 0.000 description 2
URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 2
241000894007 species Species 0.000 description 2
239000003381 stabilizer Substances 0.000 description 2
239000000126 substance Substances 0.000 description 2
125000001424 substituent group Chemical group 0.000 description 2
238000004448 titration Methods 0.000 description 2
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 1
FKTHNVSLHLHISI-UHFFFAOYSA-N 1,2-bis(isocyanatomethyl)benzene Chemical compound O=C=NCC1=CC=CC=C1CN=C=O FKTHNVSLHLHISI-UHFFFAOYSA-N 0.000 description 1
YJTKZCDBKVTVBY-UHFFFAOYSA-N 1,3-Diphenylbenzene Chemical group C1=CC=CC=C1C1=CC=CC(C=2C=CC=CC=2)=C1 YJTKZCDBKVTVBY-UHFFFAOYSA-N 0.000 description 1
150000005208 1,4-dihydroxybenzenes Chemical class 0.000 description 1
HECLRDQVFMWTQS-RGOKHQFPSA-N 1755-01-7 Chemical compound C1[C@H]2[C@@H]3CC=C[C@@H]3[C@@H]1C=C2 HECLRDQVFMWTQS-RGOKHQFPSA-N 0.000 description 1
KWVGIHKZDCUPEU-UHFFFAOYSA-N 2,2-dimethoxy-2-phenylacetophenone Chemical compound C=1C=CC=CC=1C(OC)(OC)C(=O)C1=CC=CC=C1 KWVGIHKZDCUPEU-UHFFFAOYSA-N 0.000 description 1
MTPIZGPBYCHTGQ-UHFFFAOYSA-N 2-[2,2-bis(2-prop-2-enoyloxyethoxymethyl)butoxy]ethyl prop-2-enoate Chemical compound C=CC(=O)OCCOCC(CC)(COCCOC(=O)C=C)COCCOC(=O)C=C MTPIZGPBYCHTGQ-UHFFFAOYSA-N 0.000 description 1
SVONRAPFKPVNKG-UHFFFAOYSA-N 2-ethoxyethyl acetate Chemical compound CCOCCOC(C)=O SVONRAPFKPVNKG-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
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
229920000742 Cotton Polymers 0.000 description 1
241000551547 Dione <red algae> Species 0.000 description 1
KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 1
241000233866 Fungi Species 0.000 description 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
229930192627 Naphthoquinone Natural products 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
239000004721 Polyphenylene oxide Substances 0.000 description 1
BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
239000004809 Teflon Substances 0.000 description 1
229920006362 Teflon® Polymers 0.000 description 1
ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical class [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
PSGCQDPCAWOCSH-BREBYQMCSA-N [(1r,3r,4r)-4,7,7-trimethyl-3-bicyclo[2.2.1]heptanyl] prop-2-enoate Chemical compound C1C[C@@]2(C)[C@H](OC(=O)C=C)C[C@@H]1C2(C)C PSGCQDPCAWOCSH-BREBYQMCSA-N 0.000 description 1
KXBFLNPZHXDQLV-UHFFFAOYSA-N [cyclohexyl(diisocyanato)methyl]cyclohexane Chemical compound C1CCCCC1C(N=C=O)(N=C=O)C1CCCCC1 KXBFLNPZHXDQLV-UHFFFAOYSA-N 0.000 description 1
238000005299 abrasion Methods 0.000 description 1
239000002253 acid Substances 0.000 description 1
125000003545 alkoxy group Chemical group 0.000 description 1
150000008055 alkyl aryl sulfonates 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
125000000129 anionic group Chemical group 0.000 description 1
150000004056 anthraquinones Chemical class 0.000 description 1
125000003710 aryl alkyl group Chemical group 0.000 description 1
150000004054 benzoquinones Chemical class 0.000 description 1
230000001680 brushing effect Effects 0.000 description 1
150000001728 carbonyl compounds Chemical class 0.000 description 1
239000003153 chemical reaction reagent Substances 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
238000011109 contamination Methods 0.000 description 1
229910052802 copper Inorganic materials 0.000 description 1
239000010949 copper Substances 0.000 description 1
239000002537 cosmetic Substances 0.000 description 1
230000001066 destructive effect Effects 0.000 description 1
125000004663 dialkyl amino group Chemical group 0.000 description 1
150000001991 dicarboxylic acids Chemical class 0.000 description 1
125000005442 diisocyanate group Chemical group 0.000 description 1
238000007598 dipping method Methods 0.000 description 1
GMSCBRSQMRDRCD-UHFFFAOYSA-N dodecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCOC(=O)C(C)=C GMSCBRSQMRDRCD-UHFFFAOYSA-N 0.000 description 1
239000000428 dust Substances 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
238000007687 exposure technique Methods 0.000 description 1
239000000446 fuel Substances 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
229910052739 hydrogen Inorganic materials 0.000 description 1
239000001257 hydrogen Substances 0.000 description 1
150000002440 hydroxy compounds Chemical class 0.000 description 1
239000012442 inert solvent Substances 0.000 description 1
239000000976 ink Substances 0.000 description 1
LQBJWKCYZGMFEV-UHFFFAOYSA-N lead tin Chemical compound [Sn].[Pb] LQBJWKCYZGMFEV-UHFFFAOYSA-N 0.000 description 1
238000005259 measurement Methods 0.000 description 1
239000002923 metal particle Substances 0.000 description 1
229940043265 methyl isobutyl ketone Drugs 0.000 description 1
125000001442 methylidyne group Chemical group [H]C#[*] 0.000 description 1
150000002763 monocarboxylic acids Chemical class 0.000 description 1
150000002791 naphthoquinones Chemical class 0.000 description 1
239000003921 oil Substances 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
230000037361 pathway Effects 0.000 description 1
239000003208 petroleum Substances 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 description 1
230000000704 physical effect Effects 0.000 description 1
239000004014 plasticizer Substances 0.000 description 1
238000006116 polymerization reaction Methods 0.000 description 1
239000004814 polyurethane Substances 0.000 description 1
229920002635 polyurethane Polymers 0.000 description 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
238000012545 processing Methods 0.000 description 1
230000001737 promoting effect Effects 0.000 description 1
AZIQALWHRUQPHV-UHFFFAOYSA-N prop-2-eneperoxoic acid Chemical compound OOC(=O)C=C AZIQALWHRUQPHV-UHFFFAOYSA-N 0.000 description 1
150000003254 radicals Chemical class 0.000 description 1
239000000376 reactant Substances 0.000 description 1
230000035484 reaction time Effects 0.000 description 1
239000011347 resin Substances 0.000 description 1
229920005989 resin Polymers 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
229910000077 silane Inorganic materials 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
239000011734 sodium Substances 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
229910000679 solder Inorganic materials 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000007921 spray Substances 0.000 description 1
238000005507 spraying Methods 0.000 description 1
229910001220 stainless steel Inorganic materials 0.000 description 1
239000010935 stainless steel Substances 0.000 description 1
238000003756 stirring Methods 0.000 description 1
150000003871 sulfonates Chemical class 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
150000003512 tertiary amines Chemical class 0.000 description 1
239000002562 thickening agent Substances 0.000 description 1
150000003606 tin compounds Chemical class 0.000 description 1
KSBAEPSJVUENNK-UHFFFAOYSA-L tin(ii) 2-ethylhexanoate Chemical compound [Sn+2].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O KSBAEPSJVUENNK-UHFFFAOYSA-L 0.000 description 1
DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 1
150000004072 triols Chemical class 0.000 description 1
238000005303 weighing Methods 0.000 description 1
239000008096 xylene Substances 0.000 description 1
150000003751 zinc Chemical class 0.000 description 1
CHJMFFKHPHCQIJ-UHFFFAOYSA-L zinc;octanoate Chemical compound [Zn+2].CCCCCCCC([O-])=O.CCCCCCCC([O-])=O CHJMFFKHPHCQIJ-UHFFFAOYSA-L 0.000 description 1

Landscapes

Compositions Of Macromolecular Compounds (AREA)
Paints Or Removers (AREA)
Macromonomer-Based Addition Polymer (AREA)
Structures Or Materials For Encapsulating Or Coating Semiconductor Devices Or Solid State Devices (AREA)
Non-Metallic Protective Coatings For Printed Circuits (AREA)
Polyurethanes Or Polyureas (AREA)

CA 2073155 1991-07-16 1992-07-06 Composition de vulcanisation double et utilisation de celle-ci Abandoned CA2073155A1 (fr)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US730,421		1985-05-06
US73042191A	1991-07-16	1991-07-16

Publications (1)

Publication Number	Publication Date
CA2073155A1 true CA2073155A1 (fr)	1993-01-17

Family

ID=24935291

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA 2073155 Abandoned CA2073155A1 (fr)	1991-07-16	1992-07-06	Composition de vulcanisation double et utilisation de celle-ci

Country Status (2)

Country	Link
JP (1)	JP3226337B2 (fr)
CA (1)	CA2073155A1 (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
EP1103572A3 (fr) *	1999-11-23	2001-11-07	Bayer Ag	Uréthanéacrylate contenant des groupes d'isocyanate photodurcissable et son utilisation

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE19860041A1 (de) *	1998-12-23	2000-06-29	Basf Ag	Durch Addition an Isocyanatgruppen als auch durch strahlungsinduzierte Addition an aktivierte C-C-Doppelbindungen härtbare Beschichtungsmittel
JP5280043B2 (ja) *	2007-12-12	2013-09-04	株式会社Ｄｎｐファインケミカル	液晶配向制御用突起、及びカラーフィルタ
JP5724340B2 (ja) *	2010-12-06	2015-05-27	株式会社デンソー	光硬化性防滴材
KR101552206B1 (ko)	2013-12-20	2015-09-10	조광페인트주식회사	Uv패턴 인쇄적성 도료 조성물 및 이를 이용한 uv패턴 무늬 제조방법

1992
- 1992-07-06 CA CA 2073155 patent/CA2073155A1/fr not_active Abandoned
- 1992-07-14 JP JP20862492A patent/JP3226337B2/ja not_active Expired - Fee Related

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
EP1103572A3 (fr) *	1999-11-23	2001-11-07	Bayer Ag	Uréthanéacrylate contenant des groupes d'isocyanate photodurcissable et son utilisation
US6599955B1 (en)	1999-11-23	2003-07-29	Bayer Aktiengesellschaft	Radiation-curable urethane acrylates containing iso-cyanate groups and their use

Also Published As

Publication number	Publication date
JP3226337B2 (ja)	2001-11-05
JPH05239342A (ja)	1993-09-17

Legal Events

Date	Code	Title	Description
1998-07-31	EEER	Examination request
2002-07-08	FZDE	Dead

Publication	Publication Date	Title
EP0549116B1 (fr)	1998-02-04	Méthode de rêvetement pour circuits imprimés
US4424252A (en)	1984-01-03	Conformal coating systems
US4415604A (en)	1983-11-15	Conformal coating and potting system
US4451523A (en)	1984-05-29	Conformal coating systems
EP0711802B1 (fr)	1999-10-06	Procédé pour la visualisation du durcissement de compositions durcissables à la lumière ultraviolette par un changement de couleur
US4283480A (en)	1981-08-11	Photopolymerizable compositions, methods for their preparation, and methods for their use in coating substrates
US4786586A (en)	1988-11-22	Radiation curable coating for photographic laminate
EP0618244B1 (fr)	1998-07-15	Composition multiple durcissable et son utilisation
EP0188880B1 (fr)	1989-05-31	Systèmes de revêtement épousant les formes
US5312943A (en)	1994-05-17	Dual curing conformal coatings
CA2011418A1 (fr)	1990-09-03	Revetement sechant aux ultraviolets pour pci
TW202428635A (zh)	2024-07-16	具有濕氣次要固化功能之單一組分uv可固化保形塗層
CA2073155A1 (fr)	1993-01-17	Composition de vulcanisation double et utilisation de celle-ci
AU603503B2 (en)	1990-11-15	Uv curable conformal coating with improved low temperature properties
EP0231548B1 (fr)	1991-06-12	Système de revêtement et d'encapsulation épousant les formes
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