SE449371B - I ultraviolett ljus herdbar beleggningskomposition och anvendning av denna for framstellning av en film med lag glans - Google Patents

I ultraviolett ljus herdbar beleggningskomposition och anvendning av denna for framstellning av en film med lag glans

Info

Publication number: SE449371B
Authority: SE; Sweden
Prior art keywords: coating composition; parts; photosensitizer; terminator; photoinitiator
Prior art date: 1979-02-26

Application number

SE8001376A

Other languages

English (en)

Swedish (sv)

Other versions

SE8001376L (sv

Inventor

L H Carlblom

Original Assignee

Ppg Industries Inc

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.)

1979-02-26

Filing date

1980-02-21

Publication date

1987-04-27

1980-02-21 Application filed by Ppg Industries Inc filed Critical Ppg Industries Inc

1980-08-27 Publication of SE8001376L publication Critical patent/SE8001376L/xx

1987-04-27 Publication of SE449371B publication Critical patent/SE449371B/sv

Links

239000008199 coating composition Substances 0.000 title claims description 65
-1 acrylyloxy groups Chemical group 0.000 claims description 58
239000003504 photosensitizing agent Substances 0.000 claims description 35
150000003254 radicals Chemical class 0.000 claims description 30
150000001875 compounds Chemical class 0.000 claims description 28
238000000576 coating method Methods 0.000 claims description 27
239000000178 monomer Substances 0.000 claims description 23
UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 claims description 21
239000000049 pigment Substances 0.000 claims description 18
239000011230 binding agent Substances 0.000 claims description 17
239000011248 coating agent Substances 0.000 claims description 15
239000012965 benzophenone Substances 0.000 claims description 13
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 12
RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 claims description 12
239000003999 initiator Substances 0.000 claims description 7
230000000977 initiatory effect Effects 0.000 claims description 7
238000000034 method Methods 0.000 claims description 7
239000003112 inhibitor Substances 0.000 claims description 5
238000006116 polymerization reaction Methods 0.000 claims description 5
238000010526 radical polymerization reaction Methods 0.000 claims description 5
230000005764 inhibitory process Effects 0.000 claims description 3
238000006897 homolysis reaction Methods 0.000 claims description 2
238000006552 photochemical reaction Methods 0.000 claims description 2
230000001443 photoexcitation Effects 0.000 claims description 2
238000007342 radical addition reaction Methods 0.000 claims description 2
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 claims 1
230000009089 cytolysis Effects 0.000 claims 1
125000004432 carbon atom Chemical group C* 0.000 description 45
239000000203 mixture Substances 0.000 description 40
125000000217 alkyl group Chemical group 0.000 description 21
238000006243 chemical reaction Methods 0.000 description 18
125000004386 diacrylate group Chemical group 0.000 description 17
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 16
238000002156 mixing Methods 0.000 description 16
VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 15
239000000463 material Substances 0.000 description 14
125000003545 alkoxy group Chemical group 0.000 description 13
QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 11
239000011541 reaction mixture Substances 0.000 description 11
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 10
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 9
239000007795 chemical reaction product Substances 0.000 description 8
XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 8
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ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 8
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239000004615 ingredient Substances 0.000 description 7
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239000004800 polyvinyl chloride Substances 0.000 description 7
239000002344 surface layer Substances 0.000 description 7
HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 description 6
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125000005605 benzo group Chemical group 0.000 description 6
239000001257 hydrogen Substances 0.000 description 6
229910052739 hydrogen Inorganic materials 0.000 description 6
239000007788 liquid Substances 0.000 description 6
239000000377 silicon dioxide Substances 0.000 description 6
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 5
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical class OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 5
WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 5
238000012644 addition polymerization Methods 0.000 description 5
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 5
229910052794 bromium Chemical group 0.000 description 5
239000000460 chlorine Substances 0.000 description 5
229910052801 chlorine Inorganic materials 0.000 description 5
125000001424 substituent group Chemical group 0.000 description 5
FTALTLPZDVFJSS-UHFFFAOYSA-N 2-(2-ethoxyethoxy)ethyl prop-2-enoate Chemical compound CCOCCOCCOC(=O)C=C FTALTLPZDVFJSS-UHFFFAOYSA-N 0.000 description 4
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 4
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 4
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125000003118 aryl group Chemical group 0.000 description 4
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230000015572 biosynthetic process Effects 0.000 description 4
125000005843 halogen group Chemical group 0.000 description 4
238000010438 heat treatment Methods 0.000 description 4
150000002431 hydrogen Chemical class 0.000 description 4
230000003993 interaction Effects 0.000 description 4
239000001301 oxygen Substances 0.000 description 4
229910052760 oxygen Inorganic materials 0.000 description 4
239000000523 sample Substances 0.000 description 4
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 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 3
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Natural products CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 3
NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 3
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 3
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
238000010521 absorption reaction Methods 0.000 description 3
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
239000000969 carrier Substances 0.000 description 3
238000006356 dehydrogenation reaction Methods 0.000 description 3
239000002270 dispersing agent Substances 0.000 description 3
230000000694 effects Effects 0.000 description 3
239000007789 gas Substances 0.000 description 3
230000002401 inhibitory effect Effects 0.000 description 3
239000010410 layer Substances 0.000 description 3
229910052753 mercury Inorganic materials 0.000 description 3
239000003960 organic solvent Substances 0.000 description 3
229920000642 polymer Polymers 0.000 description 3
229920002635 polyurethane Polymers 0.000 description 3
239000004814 polyurethane Substances 0.000 description 3
239000000047 product Substances 0.000 description 3
239000010453 quartz Substances 0.000 description 3
229920005989 resin Polymers 0.000 description 3
239000011347 resin Substances 0.000 description 3
239000002904 solvent Substances 0.000 description 3
239000000758 substrate Substances 0.000 description 3
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 2
OHBQPCCCRFSCAX-UHFFFAOYSA-N 1,4-Dimethoxybenzene Chemical compound COC1=CC=C(OC)C=C1 OHBQPCCCRFSCAX-UHFFFAOYSA-N 0.000 description 2
QRPDMEIIZPOYED-UHFFFAOYSA-N 1,8-dimethoxynaphthalene Chemical compound C1=CC(OC)=C2C(OC)=CC=CC2=C1 QRPDMEIIZPOYED-UHFFFAOYSA-N 0.000 description 2
WYECURVXVYPVAT-UHFFFAOYSA-N 1-(4-bromophenyl)ethanone Chemical compound CC(=O)C1=CC=C(Br)C=C1 WYECURVXVYPVAT-UHFFFAOYSA-N 0.000 description 2
NQMUGNMMFTYOHK-UHFFFAOYSA-N 1-methoxynaphthalene Chemical compound C1=CC=C2C(OC)=CC=CC2=C1 NQMUGNMMFTYOHK-UHFFFAOYSA-N 0.000 description 2
QPUYECUOLPXSFR-UHFFFAOYSA-N 1-methylnaphthalene Chemical compound C1=CC=C2C(C)=CC=CC2=C1 QPUYECUOLPXSFR-UHFFFAOYSA-N 0.000 description 2
LNETULKMXZVUST-UHFFFAOYSA-N 1-naphthoic acid Chemical compound C1=CC=C2C(C(=O)O)=CC=CC2=C1 LNETULKMXZVUST-UHFFFAOYSA-N 0.000 description 2
GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 2
XSAYZAUNJMRRIR-UHFFFAOYSA-N 2-acetylnaphthalene Chemical compound C1=CC=CC2=CC(C(=O)C)=CC=C21 XSAYZAUNJMRRIR-UHFFFAOYSA-N 0.000 description 2
ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 2
QIMMUPPBPVKWKM-UHFFFAOYSA-N 2-methylnaphthalene Chemical compound C1=CC=CC2=CC(C)=CC=C21 QIMMUPPBPVKWKM-UHFFFAOYSA-N 0.000 description 2
PJKVFARRVXDXAD-UHFFFAOYSA-N 2-naphthaldehyde Chemical compound C1=CC=CC2=CC(C=O)=CC=C21 PJKVFARRVXDXAD-UHFFFAOYSA-N 0.000 description 2
XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
FMMWHPNWAFZXNH-UHFFFAOYSA-N Benz[a]pyrene Chemical compound C1=C2C3=CC=CC=C3C=C(C=C3)C2=C2C3=CC=CC2=C1 FMMWHPNWAFZXNH-UHFFFAOYSA-N 0.000 description 2
KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
IRIAEXORFWYRCZ-UHFFFAOYSA-N Butylbenzyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCC1=CC=CC=C1 IRIAEXORFWYRCZ-UHFFFAOYSA-N 0.000 description 2
SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 2
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
101100298295 Drosophila melanogaster flfl gene Proteins 0.000 description 2
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239000004952 Polyamide Substances 0.000 description 2
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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
239000002253 acid Substances 0.000 description 2
NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
125000001931 aliphatic group Chemical group 0.000 description 2
125000004414 alkyl thio group Chemical group 0.000 description 2
229910052782 aluminium Inorganic materials 0.000 description 2
RDOXTESZEPMUJZ-UHFFFAOYSA-N anisole Chemical compound COC1=CC=CC=C1 RDOXTESZEPMUJZ-UHFFFAOYSA-N 0.000 description 2
125000005110 aryl thio group Chemical group 0.000 description 2
125000004104 aryloxy group Chemical group 0.000 description 2
239000012298 atmosphere 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
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150000001555 benzenes Chemical class 0.000 description 2
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 2
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125000001309 chloro group Chemical group Cl* 0.000 description 2
PJANXHGTPQOBST-QXMHVHEDSA-N cis-stilbene Chemical compound C=1C=CC=CC=1/C=C\C1=CC=CC=C1 PJANXHGTPQOBST-QXMHVHEDSA-N 0.000 description 2
238000001816 cooling Methods 0.000 description 2
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238000012546 transfer Methods 0.000 description 2
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229910052984 zinc sulfide Inorganic materials 0.000 description 1
DRDVZXDWVBGGMH-UHFFFAOYSA-N zinc;sulfide Chemical compound [S-2].[Zn+2] DRDVZXDWVBGGMH-UHFFFAOYSA-N 0.000 description 1
OENHQHLEOONYIE-JLTXGRSLSA-N β-Carotene Chemical compound CC=1CCCC(C)(C)C=1\C=C\C(\C)=C\C=C\C(\C)=C\C=C\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C OENHQHLEOONYIE-JLTXGRSLSA-N 0.000 description 1
PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-Caprolactone Chemical compound O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 0.000 description 1

Classifications

- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D3/00—Pretreatment of surfaces to which liquids or other fluent materials are to be applied; After-treatment of applied coatings, e.g. intermediate treating of an applied coating preparatory to subsequent applications of liquids or other fluent materials
- B05D3/06—Pretreatment of surfaces to which liquids or other fluent materials are to be applied; After-treatment of applied coatings, e.g. intermediate treating of an applied coating preparatory to subsequent applications of liquids or other fluent materials by exposure to radiation
- 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
- C09D4/00—Coating compositions, e.g. paints, varnishes or lacquers, based on organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond ; Coating compositions, based on monomers of macromolecular compounds of groups C09D183/00 - C09D183/16

Landscapes

Chemical & Material Sciences (AREA)
Engineering & Computer Science (AREA)
Life Sciences & Earth Sciences (AREA)
Materials Engineering (AREA)
Wood Science & Technology (AREA)
Organic Chemistry (AREA)
Physics & Mathematics (AREA)
Plasma & Fusion (AREA)
Paints Or Removers (AREA)
Polymerisation Methods In General (AREA)
Application Of Or Painting With Fluid Materials (AREA)

SE8001376A 1979-02-26 1980-02-21 I ultraviolett ljus herdbar beleggningskomposition och anvendning av denna for framstellning av en film med lag glans SE449371B (sv)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US06/015,544 US4229274A (en)	1979-02-26	1979-02-26	Ultraviolet light curable compositions for producing coatings of low gloss

Publications (2)

Publication Number	Publication Date
SE8001376L SE8001376L (sv)	1980-08-27
SE449371B true SE449371B (sv)	1987-04-27

Family

ID=21772011

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SE8001376A SE449371B (sv)	1979-02-26	1980-02-21	I ultraviolett ljus herdbar beleggningskomposition och anvendning av denna for framstellning av en film med lag glans

Country Status (10)

Country	Link
US (1)	US4229274A (de)
JP (1)	JPS55120670A (de)
AU (1)	AU517486B2 (de)
BE (1)	BE881896A (de)
CA (1)	CA1148690A (de)
DE (1)	DE3006960C2 (de)
FR (1)	FR2449714A1 (de)
GB (1)	GB2044278B (de)
IT (1)	IT1133060B (de)
SE (1)	SE449371B (de)

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US4457766A (en) *	1980-10-08	1984-07-03	Kennecott Corporation	Resin systems for high energy electron curable resin coated webs
US4514271A (en) *	1981-07-02	1985-04-30	Gaf Corporation	Stable dispersion of alkylated polyvinylpyrrolidone and vinyl pyrrolidone
US4411931A (en) *	1982-09-29	1983-10-25	Armstrong World Industries, Inc.	Multiple step UV curing process for providing accurately controlled surface texture
US4519883A (en) *	1983-06-06	1985-05-28	Stauffer Chemical Company	Sensitization of glyoxylate photoinitiators using a terphenyl compound
US6376569B1 (en) *	1990-12-13	2002-04-23	3M Innovative Properties Company	Hydrosilation reaction utilizing a (cyclopentadiene)(sigma-aliphatic) platinum complex and a free radical photoinitiator
US6046250A (en) *	1990-12-13	2000-04-04	3M Innovative Properties Company	Hydrosilation reaction utilizing a free radical photoinitiator
EP0662991A1 (de) *	1992-09-30	1995-07-19	Ppg Industries, Inc.	Pigmentierte zusammensetzungen und verfahren zur herstellung von strahlungshärtbaren beschichtungsmitteln mit einem sehr schwachen glanz
JPH06172471A (ja) *	1992-10-09	1994-06-21	Henkel Hakusui Kk	重合硬化性組成物とこれを用いて成形または被覆する方法
US6022050A (en) *	1998-09-02	2000-02-08	Monarch Marking Systems, Inc.	Silicone release coating composition
US6426034B1 (en) *	2000-10-31	2002-07-30	Lilly Industries, Inc.	Radiation curable coating for thermoplastic substrates
US6759096B2 (en)	2001-09-24	2004-07-06	Congoleum Corporation	Method for making differential gloss coverings
KR100813953B1 (ko) *	2002-04-22	2008-03-14	삼성전자주식회사	대전방지성을 갖는 광경화성 수지 조성물
MXPA04010254A (es) *	2002-04-26	2005-02-03	Ciba Sc Holding Ag	Fotoiniciado incorporable.
US20100242299A1 (en) *	2003-01-09	2010-09-30	Con-Trol-Cure, Inc.	Uv curing system and process
US20050214674A1 (en) *	2004-03-25	2005-09-29	Yu Sui	Positive-working photoimageable bottom antireflective coating
EP1760121B1 (de) *	2005-08-31	2009-10-07	FUJIFILM Corporation	Strahlungshärtbare Tinte enthaltend einen kondensierten polycyclischen aromatischen Photosensibilisator
US20070286962A1 (en) *	2006-06-09	2007-12-13	Brown Randall R	Methods for producing non-glossy coatings from radiation curable compositions
US20080152829A1 (en) *	2006-12-20	2008-06-26	Dean Roy E	Coating compositions, coatings formed therefrom and methods of making the same
US8088548B2 (en)	2007-10-23	2012-01-03	Az Electronic Materials Usa Corp.	Bottom antireflective coating compositions
EP2123265B1 (de) *	2008-05-23	2012-05-23	NOVAERA S.r.l.	Endipalenformulierungen bei der Behandlung von Psoriasis
US8455176B2 (en) *	2008-11-12	2013-06-04	Az Electronic Materials Usa Corp.	Coating composition
US8632948B2 (en) *	2009-09-30	2014-01-21	Az Electronic Materials Usa Corp.	Positive-working photoimageable bottom antireflective coating
US20110086312A1 (en) *	2009-10-09	2011-04-14	Dammel Ralph R	Positive-Working Photoimageable Bottom Antireflective Coating
US8906468B2 (en)	2011-10-27	2014-12-09	Ppg Industries Ohio, Inc.	Low gloss UV-cured coatings for aircraft
JP6451627B2 (ja) *	2014-03-11	2019-01-16	三菱ケミカル株式会社	活性エネルギー線硬化性樹脂組成物及び自動車ヘッドランプレンズ

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GB1159551A (en) *	1965-08-13	1969-07-30	Ford Motor Co	Painting
US3918393A (en) *	1971-09-10	1975-11-11	Ppg Industries Inc	Method of producing flat (non-glossy) films
US3840448A (en) *	1972-06-26	1974-10-08	Union Carbide Corp	Surface curing of acrylyl or methacrylyl compounds using radiation of 2,537 angstroms
US3874906A (en) *	1972-09-22	1975-04-01	Ppg Industries Inc	Process for applying polyester-acrylate containing ionizing irradiation curable coatings
US3915824A (en) *	1973-03-30	1975-10-28	Scm Corp	Uv and laser curing of the polymerizable binder
US4005244A (en) *	1974-09-30	1977-01-25	Ppg Industries, Inc.	Ultraviolet light curable opacifying compositions
US4017652A (en) *	1974-10-23	1977-04-12	Ppg Industries, Inc.	Photocatalyst system and ultraviolet light curable coating compositions containing the same
US4048036A (en) *	1974-10-24	1977-09-13	Ppg Industries, Inc.	Process for producing films of low gloss by exposure to ultraviolet light
US3992275A (en) *	1974-11-25	1976-11-16	Celanese Corporation	Low gloss ultraviolet curable coatings utilizing α,α,α-trichlorotoluene as a photoinitiator
US4113592A (en) *	1975-04-14	1978-09-12	Celanese Corporation	Trihalogenated hydrocarbons as co-photoinitiators
DE2702660C3 (de) *	1976-01-27	1980-07-10	Ppg Industries, Inc., Pittsburgh, Pa. (V.St.A.)	Durch Strahlung härtbare Überzugsmasse und Verfahren zu ihrer Herstellung
US4131529A (en) *	1976-06-05	1978-12-26	Basf Aktiengesellschaft	Photoinitiators for photopolymerizable coating compositions
JPS5376385A (en) *	1976-12-17	1978-07-06	Mitsubishi Electric Corp	Manufacturing method for insulated electrical wires
JPS541758A (en) *	1977-06-03	1979-01-08	Nippon Denso Co Ltd	Two stage change-over system transmission mechanism
JPS6035195B2 (ja) *	1977-10-04	1985-08-13	三菱レイヨン株式会社	光硬化型樹脂組成物の硬化法
JPS54130633A (en) *	1978-04-01	1979-10-11	Nippon Synthetic Chem Ind Co Ltd:The	Ultraviolet-curing coating composition

1979
- 1979-02-26 US US06/015,544 patent/US4229274A/en not_active Expired - Lifetime
1980
- 1980-01-08 AU AU54453/80A patent/AU517486B2/en not_active Ceased
- 1980-01-10 CA CA000343407A patent/CA1148690A/en not_active Expired
- 1980-01-16 JP JP343480A patent/JPS55120670A/ja active Granted
- 1980-02-04 IT IT67166/80A patent/IT1133060B/it active
- 1980-02-21 SE SE8001376A patent/SE449371B/sv not_active IP Right Cessation
- 1980-02-22 FR FR8003992A patent/FR2449714A1/fr active Granted
- 1980-02-25 DE DE3006960A patent/DE3006960C2/de not_active Expired
- 1980-02-25 BE BE0/199530A patent/BE881896A/fr not_active IP Right Cessation
- 1980-02-25 GB GB8006226A patent/GB2044278B/en not_active Expired

Also Published As

Publication number	Publication date
FR2449714A1 (fr)	1980-09-19
AU5445380A (en)	1980-09-18
DE3006960A1 (de)	1980-08-28
BE881896A (fr)	1980-08-25
IT8067166A0 (it)	1980-02-04
JPS55120670A (en)	1980-09-17
CA1148690A (en)	1983-06-21
SE8001376L (sv)	1980-08-27
DE3006960C2 (de)	1983-06-09
GB2044278B (en)	1983-09-28
FR2449714B1 (de)	1982-02-05
GB2044278A (en)	1980-10-15
AU517486B2 (en)	1981-08-06
JPS632993B2 (de)	1988-01-21
IT1133060B (it)	1986-07-09
US4229274A (en)	1980-10-21

Publication	Publication Date	Title
SE449371B (sv)	1987-04-27	I ultraviolett ljus herdbar beleggningskomposition och anvendning av denna for framstellning av en film med lag glans
US4017652A (en)	1977-04-12	Photocatalyst system and ultraviolet light curable coating compositions containing the same
CN100430385C (zh)	2008-11-05	改善光引发剂贮存稳定性的化合物及其用途
FI71322C (fi)	1986-12-19	Acylfosfinoxidfoereningar och deras anvaendning
Glöckner	2009	Radiation curing
JP5313873B2 (ja)	2013-10-09	スルホニウム塩開始剤
CA1340057C (en)	1998-09-22	Radiation curable compositions based on unsaturated polyesters and compounds having at least two vinyl ether groups
BE1006011A4 (fr)	1994-04-19	Oxydes d'alkyl-bis-acyl-phosphines et leur application comme photo-amorceurs pour la polymerisation de composes ethyleniques.
US4134813A (en)	1979-01-16	Photopolymerizable composition and its use
US4323591A (en)	1982-04-06	Irradiation of polyacrylate films in air
ITMI20002715A1 (it)	2002-06-15	Sali di iodonio come donatori di acidi latenti
JP2008533273A (ja)	2008-08-21	紫外線硬化性樹脂組成物
JP2010505977A (ja)	2010-02-25	フェニルグリオキシレート型の光開始剤を含む光硬化性組成物
CN103930472A (zh)	2014-07-16	一种通过电子束辐射、并通过气体产生的等离子和紫外辐射进行固化组合物的方法
US4024296A (en)	1977-05-17	Photocatalyst system and pigmented actinic light polymerizable coating compositions containing the same
DE2512642C3 (de)	1978-07-13	Durch aktinische Strahlung härtbare Masse
US4024297A (en)	1977-05-17	Actinic light polymerizable coating compositions
TWI298113B (en)	2008-06-21	Photoresist resin commposition for printing electric-circuit board
EP0304886B1 (de)	1993-12-08	Oligomere Benzilketale und ihre Verwendung als Photoinitiatoren
US4268576A (en)	1981-05-19	Stencil sheet with solventless coating and method of preparation
US3988228A (en)	1976-10-26	Photopolymerizable polymeric compositions containing halogen containing aromatic ketones
KR100959231B1 (ko)	2010-05-19	경화성 조성물, 경화막, 반사 방지막, 및 경화막의 제조방법
CA2032919A1 (en)	1991-06-23	Process for obtaining textured coatings from photo-curable urea-containing compositions
CN111324009A (zh)	2020-06-23	光固化组合物及其应用
CA1204016A (en)	1986-05-06	Actinic light polymerizable coating compositions and method of using the same

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