NO131842B - - Google Patents

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Publication number: NO131842B
Authority: NO; Norway
Prior art keywords: weight; parts; mixture; polyester resin; benzoin
Prior art date: 1970-02-05

Application number

NO412/71A

Other languages

English (en)

Norwegian (no)

Other versions

NO131842C (fr

Inventor

H Delius

B Behrens

Original Assignee

Hoechst Ag

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.)

1970-02-05

Filing date

1971-02-04

Publication date

1975-05-05

1970-02-05 Priority claimed from CH162670A external-priority patent/CH545329A/de

1970-02-05 Priority claimed from CH162770A external-priority patent/CH534705A/de

1971-01-05 Priority claimed from CH5771A external-priority patent/CH573461A5/de

1971-01-05 Priority claimed from CH5871A external-priority patent/CH579601A5/de

1971-02-04 Application filed by Hoechst Ag filed Critical Hoechst Ag

1975-05-05 Publication of NO131842B publication Critical patent/NO131842B/no

1975-08-13 Publication of NO131842C publication Critical patent/NO131842C/no

Links

239000000203 mixture Substances 0.000 claims description 64
-1 cycloaliphatic Chemical group 0.000 claims description 39
238000000576 coating method Methods 0.000 claims description 26
239000011248 coating agent Substances 0.000 claims description 24
238000002360 preparation method Methods 0.000 claims description 22
150000001875 compounds Chemical class 0.000 claims description 20
229920006337 unsaturated polyester resin Polymers 0.000 claims description 20
239000012188 paraffin wax Substances 0.000 claims description 17
229920001225 polyester resin Polymers 0.000 claims description 17
239000004645 polyester resin Substances 0.000 claims description 17
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 16
238000009281 ultraviolet germicidal irradiation Methods 0.000 claims description 12
239000000178 monomer Substances 0.000 claims description 11
125000003118 aryl group Chemical group 0.000 claims description 9
229910000147 aluminium phosphate Inorganic materials 0.000 claims description 8
150000002148 esters Chemical class 0.000 claims description 8
238000005470 impregnation Methods 0.000 claims description 8
238000007605 air drying Methods 0.000 claims description 7
229910052751 metal Inorganic materials 0.000 claims description 7
239000002184 metal Substances 0.000 claims description 7
NLGDWWCZQDIASO-UHFFFAOYSA-N 2-hydroxy-1-(7-oxabicyclo[4.1.0]hepta-1,3,5-trien-2-yl)-2-phenylethanone Chemical compound OC(C(=O)c1cccc2Oc12)c1ccccc1 NLGDWWCZQDIASO-UHFFFAOYSA-N 0.000 claims description 6
150000003003 phosphines Chemical class 0.000 claims description 6
238000000465 moulding Methods 0.000 claims description 5
239000003505 polymerization initiator Substances 0.000 claims description 5
239000000126 substance Substances 0.000 claims description 5
125000001931 aliphatic group Chemical group 0.000 claims description 2
125000000623 heterocyclic group Chemical group 0.000 claims description 2
150000003014 phosphoric acid esters Chemical class 0.000 claims description 2
150000003018 phosphorus compounds Chemical class 0.000 claims description 2
125000001424 substituent group Chemical group 0.000 claims description 2
239000001993 wax Substances 0.000 claims description 2
RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 56
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 52
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 40
238000001723 curing Methods 0.000 description 27
QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 24
ISAOCJYIOMOJEB-UHFFFAOYSA-N desyl alcohol Natural products C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 0.000 description 21
KMNCBSZOIQAUFX-UHFFFAOYSA-N 2-ethoxy-1,2-diphenylethanone Chemical compound C=1C=CC=CC=1C(OCC)C(=O)C1=CC=CC=C1 KMNCBSZOIQAUFX-UHFFFAOYSA-N 0.000 description 20
244000028419 Styrax benzoin Species 0.000 description 19
235000000126 Styrax benzoin Nutrition 0.000 description 19
235000008411 Sumatra benzointree Nutrition 0.000 description 19
229960002130 benzoin Drugs 0.000 description 19
235000019382 gum benzoic Nutrition 0.000 description 19
238000012360 testing method Methods 0.000 description 18
238000001879 gelation Methods 0.000 description 15
238000000034 method Methods 0.000 description 15
239000002253 acid Substances 0.000 description 13
229920000728 polyester Polymers 0.000 description 13
238000001816 cooling Methods 0.000 description 12
238000003848 UV Light-Curing Methods 0.000 description 11
239000011521 glass Substances 0.000 description 10
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 9
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 9
239000000463 material Substances 0.000 description 9
QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 9
238000003860 storage Methods 0.000 description 9
239000000758 substrate Substances 0.000 description 9
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 8
LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 8
JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 8
OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 8
239000003365 glass fiber Substances 0.000 description 8
150000002978 peroxides Chemical class 0.000 description 8
229920006305 unsaturated polyester Polymers 0.000 description 8
230000000052 comparative effect Effects 0.000 description 7
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 6
238000004519 manufacturing process Methods 0.000 description 6
150000001298 alcohols Chemical class 0.000 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 description 5
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 5
229910000073 phosphorus hydride Inorganic materials 0.000 description 5
239000004033 plastic Substances 0.000 description 5
229920003023 plastic Polymers 0.000 description 5
239000011120 plywood Substances 0.000 description 5
230000008569 process Effects 0.000 description 5
LVTJOONKWUXEFR-FZRMHRINSA-N protoneodioscin Natural products O(C[C@@H](CC[C@]1(O)[C@H](C)[C@@H]2[C@]3(C)[C@H]([C@H]4[C@@H]([C@]5(C)C(=CC4)C[C@@H](O[C@@H]4[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@@H](O)[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@H](CO)O4)CC5)CC3)C[C@@H]2O1)C)[C@H]1[C@H](O)[C@H](O)[C@H](O)[C@@H](CO)O1 LVTJOONKWUXEFR-FZRMHRINSA-N 0.000 description 5
239000002966 varnish Substances 0.000 description 5
XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 description 4
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 4
239000003795 chemical substances by application Substances 0.000 description 4
150000001991 dicarboxylic acids Chemical class 0.000 description 4
LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
238000011049 filling Methods 0.000 description 4
239000011888 foil Substances 0.000 description 4
238000005259 measurement Methods 0.000 description 4
238000006116 polymerization reaction Methods 0.000 description 4
230000005855 radiation Effects 0.000 description 4
150000005846 sugar alcohols Polymers 0.000 description 4
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 4
FEVFLQDDNUQKRY-UHFFFAOYSA-N tris(4-methylphenyl) phosphite Chemical compound C1=CC(C)=CC=C1OP(OC=1C=CC(C)=CC=1)OC1=CC=C(C)C=C1 FEVFLQDDNUQKRY-UHFFFAOYSA-N 0.000 description 4
WXAZIUYTQHYBFW-UHFFFAOYSA-N tris(4-methylphenyl)phosphane Chemical compound C1=CC(C)=CC=C1P(C=1C=CC(C)=CC=1)C1=CC=C(C)C=C1 WXAZIUYTQHYBFW-UHFFFAOYSA-N 0.000 description 4
MMEDJBFVJUFIDD-UHFFFAOYSA-N 2-[2-(carboxymethyl)phenyl]acetic acid Chemical compound OC(=O)CC1=CC=CC=C1CC(O)=O MMEDJBFVJUFIDD-UHFFFAOYSA-N 0.000 description 3
WFUGQJXVXHBTEM-UHFFFAOYSA-N 2-hydroperoxy-2-(2-hydroperoxybutan-2-ylperoxy)butane Chemical compound CCC(C)(OO)OOC(C)(CC)OO WFUGQJXVXHBTEM-UHFFFAOYSA-N 0.000 description 3
AXYQEGMSGMXGGK-UHFFFAOYSA-N 2-phenoxy-1,2-diphenylethanone Chemical compound C=1C=CC=CC=1C(=O)C(C=1C=CC=CC=1)OC1=CC=CC=C1 AXYQEGMSGMXGGK-UHFFFAOYSA-N 0.000 description 3
FYRWKWGEFZTOQI-UHFFFAOYSA-N 3-prop-2-enoxy-2,2-bis(prop-2-enoxymethyl)propan-1-ol Chemical compound C=CCOCC(CO)(COCC=C)COCC=C FYRWKWGEFZTOQI-UHFFFAOYSA-N 0.000 description 3
229910002012 Aerosil® Inorganic materials 0.000 description 3
239000005749 Copper compound Substances 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 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
150000008064 anhydrides Chemical class 0.000 description 3
238000005452 bending Methods 0.000 description 3
235000011132 calcium sulphate Nutrition 0.000 description 3
239000001175 calcium sulphate Substances 0.000 description 3
229910017052 cobalt Inorganic materials 0.000 description 3
239000010941 cobalt Substances 0.000 description 3
GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 3
238000009833 condensation Methods 0.000 description 3
230000005494 condensation Effects 0.000 description 3
150000001880 copper compounds Chemical class 0.000 description 3
239000001530 fumaric acid Substances 0.000 description 3
125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
239000004922 lacquer Substances 0.000 description 3
238000002844 melting Methods 0.000 description 3
230000008018 melting Effects 0.000 description 3
WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 3
239000000047 product Substances 0.000 description 3
230000009257 reactivity Effects 0.000 description 3
230000002787 reinforcement Effects 0.000 description 3
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 3
239000002023 wood Substances 0.000 description 3
KMOUUZVZFBCRAM-OLQVQODUSA-N (3as,7ar)-3a,4,7,7a-tetrahydro-2-benzofuran-1,3-dione Chemical compound C1C=CC[C@@H]2C(=O)OC(=O)[C@@H]21 KMOUUZVZFBCRAM-OLQVQODUSA-N 0.000 description 2
MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 description 2
KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical group CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 2
QEDJMOONZLUIMC-UHFFFAOYSA-N 1-tert-butyl-4-ethenylbenzene Chemical compound CC(C)(C)C1=CC=C(C=C)C=C1 QEDJMOONZLUIMC-UHFFFAOYSA-N 0.000 description 2
OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 2
BKQRBKNZMLWPDY-UHFFFAOYSA-N 2-(2-ethylhexoxy)-1,2-diphenylethanone Chemical compound C=1C=CC=CC=1C(OCC(CC)CCCC)C(=O)C1=CC=CC=C1 BKQRBKNZMLWPDY-UHFFFAOYSA-N 0.000 description 2
XFCMNSHQOZQILR-UHFFFAOYSA-N 2-[2-(2-methylprop-2-enoyloxy)ethoxy]ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCOC(=O)C(C)=C XFCMNSHQOZQILR-UHFFFAOYSA-N 0.000 description 2
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 2
DZZAHLOABNWIFA-UHFFFAOYSA-N 2-butoxy-1,2-diphenylethanone Chemical compound C=1C=CC=CC=1C(OCCCC)C(=O)C1=CC=CC=C1 DZZAHLOABNWIFA-UHFFFAOYSA-N 0.000 description 2
YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-ethylhexan-1-ol Chemical group CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 description 2
YCOXTKKNXUZSKD-UHFFFAOYSA-N 3,4-xylenol Chemical compound CC1=CC=C(O)C=C1C YCOXTKKNXUZSKD-UHFFFAOYSA-N 0.000 description 2
DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 2
BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 2
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 2
KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 2
239000000853 adhesive Substances 0.000 description 2
230000001070 adhesive effect Effects 0.000 description 2
WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
230000001476 alcoholic effect Effects 0.000 description 2
XXROGKLTLUQVRX-UHFFFAOYSA-N allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 description 2
ZCGHEBMEQXMRQL-UHFFFAOYSA-N benzyl 2-carbamoylpyrrolidine-1-carboxylate Chemical compound NC(=O)C1CCCN1C(=O)OCC1=CC=CC=C1 ZCGHEBMEQXMRQL-UHFFFAOYSA-N 0.000 description 2
MKUWVMRNQOOSAT-UHFFFAOYSA-N but-3-en-2-ol Chemical compound CC(O)C=C MKUWVMRNQOOSAT-UHFFFAOYSA-N 0.000 description 2
239000011093 chipboard Substances 0.000 description 2
NMAKPIATXQEXBT-UHFFFAOYSA-N didecyl phenyl phosphite Chemical compound CCCCCCCCCCOP(OCCCCCCCCCC)OC1=CC=CC=C1 NMAKPIATXQEXBT-UHFFFAOYSA-N 0.000 description 2
LVTCZSBUROAWTE-UHFFFAOYSA-N diethyl(phenyl)phosphane Chemical compound CCP(CC)C1=CC=CC=C1 LVTCZSBUROAWTE-UHFFFAOYSA-N 0.000 description 2
238000002845 discoloration Methods 0.000 description 2
LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical group CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 2
230000000694 effects Effects 0.000 description 2
150000002170 ethers Chemical class 0.000 description 2
238000002474 experimental method Methods 0.000 description 2
239000000945 filler Substances 0.000 description 2
LHGVFZTZFXWLCP-UHFFFAOYSA-N guaiacol Chemical compound COC1=CC=CC=C1O LHGVFZTZFXWLCP-UHFFFAOYSA-N 0.000 description 2
FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 2
230000006872 improvement Effects 0.000 description 2
239000003112 inhibitor Substances 0.000 description 2
238000011835 investigation Methods 0.000 description 2
ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
238000003475 lamination Methods 0.000 description 2
UJNZOIKQAUQOCN-UHFFFAOYSA-N methyl(diphenyl)phosphane Chemical compound C=1C=CC=CC=1P(C)C1=CC=CC=C1 UJNZOIKQAUQOCN-UHFFFAOYSA-N 0.000 description 2
ZWRUINPWMLAQRD-UHFFFAOYSA-N nonan-1-ol Chemical group CCCCCCCCCO ZWRUINPWMLAQRD-UHFFFAOYSA-N 0.000 description 2
GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical group CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 2
NWVVVBRKAWDGAB-UHFFFAOYSA-N p-methoxyphenol Chemical compound COC1=CC=C(O)C=C1 NWVVVBRKAWDGAB-UHFFFAOYSA-N 0.000 description 2
229910052698 phosphorus Inorganic materials 0.000 description 2
239000011574 phosphorus Substances 0.000 description 2
XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
239000000049 pigment Substances 0.000 description 2
239000002685 polymerization catalyst Substances 0.000 description 2
239000011148 porous material Substances 0.000 description 2
150000003138 primary alcohols Chemical class 0.000 description 2
230000009467 reduction Effects 0.000 description 2
229920006395 saturated elastomer Polymers 0.000 description 2
230000003678 scratch resistant effect Effects 0.000 description 2
CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 2
235000012239 silicon dioxide Nutrition 0.000 description 2
229920002545 silicone oil Polymers 0.000 description 2
230000002195 synergetic effect Effects 0.000 description 2
239000000454 talc Substances 0.000 description 2
235000012222 talc Nutrition 0.000 description 2
229910052623 talc Inorganic materials 0.000 description 2
QXJQHYBHAIHNGG-UHFFFAOYSA-N trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-UHFFFAOYSA-N 0.000 description 2
NIDNOXCRFUCAKQ-UMRXKNAASA-N (1s,2r,3s,4r)-bicyclo[2.2.1]hept-5-ene-2,3-dicarboxylic acid Chemical compound C1[C@H]2C=C[C@@H]1[C@H](C(=O)O)[C@@H]2C(O)=O NIDNOXCRFUCAKQ-UMRXKNAASA-N 0.000 description 1
DJKGDNKYTKCJKD-BPOCMEKLSA-N (1s,4r,5s,6r)-1,2,3,4,7,7-hexachlorobicyclo[2.2.1]hept-2-ene-5,6-dicarboxylic acid Chemical compound ClC1=C(Cl)[C@]2(Cl)[C@H](C(=O)O)[C@H](C(O)=O)[C@@]1(Cl)C2(Cl)Cl DJKGDNKYTKCJKD-BPOCMEKLSA-N 0.000 description 1
BCDQZAMNBUEUES-UHFFFAOYSA-N (4-bromophenyl)-bis(ethenyl)phosphane Chemical compound BrC1=CC=C(P(C=C)C=C)C=C1 BCDQZAMNBUEUES-UHFFFAOYSA-N 0.000 description 1
239000001124 (E)-prop-1-ene-1,2,3-tricarboxylic acid Substances 0.000 description 1
DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 1
OOCCDEMITAIZTP-DAXSKMNVSA-N (Z)-cinnamyl alcohol Chemical compound OC\C=C/C1=CC=CC=C1 OOCCDEMITAIZTP-DAXSKMNVSA-N 0.000 description 1
ZQHJVIHCDHJVII-OWOJBTEDSA-N (e)-2-chlorobut-2-enedioic acid Chemical compound OC(=O)\C=C(\Cl)C(O)=O ZQHJVIHCDHJVII-OWOJBTEDSA-N 0.000 description 1
MSAHTMIQULFMRG-UHFFFAOYSA-N 1,2-diphenyl-2-propan-2-yloxyethanone Chemical compound C=1C=CC=CC=1C(OC(C)C)C(=O)C1=CC=CC=C1 MSAHTMIQULFMRG-UHFFFAOYSA-N 0.000 description 1
QWQFVUQPHUKAMY-UHFFFAOYSA-N 1,2-diphenyl-2-propoxyethanone Chemical compound C=1C=CC=CC=1C(OCCC)C(=O)C1=CC=CC=C1 QWQFVUQPHUKAMY-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
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Classifications

- E—FIXED CONSTRUCTIONS
- E04—BUILDING
- E04C—STRUCTURAL ELEMENTS; BUILDING MATERIALS
- E04C2/00—Building elements of relatively thin form for the construction of parts of buildings, e.g. sheet materials, slabs, or panels
- E04C2/02—Building elements of relatively thin form for the construction of parts of buildings, e.g. sheet materials, slabs, or panels characterised by specified materials
- E04C2/10—Building elements of relatively thin form for the construction of parts of buildings, e.g. sheet materials, slabs, or panels characterised by specified materials of wood, fibres, chips, vegetable stems, or the like; of plastics; of foamed products
- E04C2/24—Building elements of relatively thin form for the construction of parts of buildings, e.g. sheet materials, slabs, or panels characterised by specified materials of wood, fibres, chips, vegetable stems, or the like; of plastics; of foamed products laminated and composed of materials covered by two or more of groups E04C2/12, E04C2/16, E04C2/20
- 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
- C08F283/00—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G
- C08F283/006—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G on to polymers provided for in C08G18/00
- 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
- C08F283/00—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G
- C08F283/01—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G on to unsaturated polyesters
- 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
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
- C08G63/12—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
- C08G63/52—Polycarboxylic acids or polyhydroxy compounds in which at least one of the two components contains aliphatic unsaturation
- C08G63/54—Polycarboxylic acids or polyhydroxy compounds in which at least one of the two components contains aliphatic unsaturation the acids or hydroxy compounds containing carbocyclic rings
- C08G63/553—Acids or hydroxy compounds containing cycloaliphatic rings, e.g. Diels-Alder adducts
- 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
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/07—Aldehydes; Ketones
- 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
- C08K5/00—Use of organic ingredients
- C08K5/49—Phosphorus-containing compounds
- C08K5/51—Phosphorus bound to oxygen
- C08K5/52—Phosphorus bound to oxygen only
- C08K5/524—Esters of phosphorous acids, e.g. of H3PO3

Landscapes

Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Engineering & Computer Science (AREA)
Architecture (AREA)
Wood Science & Technology (AREA)
Life Sciences & Earth Sciences (AREA)
Civil Engineering (AREA)
Structural Engineering (AREA)
Macromonomer-Based Addition Polymer (AREA)
Paints Or Removers (AREA)
Application Of Or Painting With Fluid Materials (AREA)
Polymerisation Methods In General (AREA)

NO412/71A 1970-02-05 1971-02-04 NO131842C (fr)

Applications Claiming Priority (4)

Application Number	Priority Date	Filing Date	Title
CH162670A CH545329A (de)	1970-02-05	1970-02-05	Durch UV-Bestrahlung härtbare Zubereitungen auf Grundlage ungesättigter Polyesterharze
CH162770A CH534705A (de)	1970-02-05	1970-02-05	Verfahren zur Herstellung von Formkörpern, Imprägnierungen und Ueberzügen
CH5771A CH573461A5 (en)	1971-01-05	1971-01-05	Photochemically polymerisable polyester moulding composn
CH5871A CH579601A5 (en)	1971-01-05	1971-01-05	Photochemically polymerisable polyester moulding composn

Publications (2)

Publication Number	Publication Date
NO131842B true NO131842B (fr)	1975-05-05
NO131842C NO131842C (fr)	1975-08-13

Family

ID=27427749

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO412/71A NO131842C (fr)	1970-02-05	1971-02-04

Country Status (9)

Country	Link
US (1)	US3699022A (fr)
JP (1)	JPS515439B1 (fr)
BE (1)	BE762509A (fr)
DE (2)	DE2104958C3 (fr)
DK (1)	DK135173B (fr)
FI (1)	FI50794C (fr)
FR (1)	FR2079275A1 (fr)
NO (1)	NO131842C (fr)
SE (1)	SE371447B (fr)

Families Citing this family (20)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4020193A (en) *	1971-04-20	1977-04-26	Ppg Industries, Inc.	Method of forming a non-glossy film
JPS5010627B1 (fr) *	1971-06-09	1975-04-23
GB1408265A (en) *	1971-10-18	1975-10-01	Ici Ltd	Photopolymerisable composition
US3933875A (en) *	1972-03-11	1976-01-20	Basf Farben & Fasern Ag	Opaque polyester copolymer coated articles
US3993798A (en) *	1972-06-19	1976-11-23	Basf Farben & Fasern Aktiengesellschaft	Cured opaque coating with high hiding power produced from normally transparent polyester paste filler compositions
DE2251469C3 (de) *	1972-10-20	1978-06-08	Bayer Ag, 5090 Leverkusen	Hochreaktive, durch UV-Licht härtbare Harzmassen, die Acrylamidmethyloläther enthalten
US4107391A (en) *	1973-12-10	1978-08-15	General Electric Company	Method for making thermoformable composites and composites made thereby
GB1538211A (en) *	1975-05-12	1979-01-10	Ucb Sa	Halogenated photopolymerisable adhesives
GB1538436A (en) *	1975-05-12	1979-01-17	Ucb Sa	Halogenated photopolymerisable compositions
GB1553580A (en) *	1975-11-21	1979-09-26	Espe Pharm Praep	Photopolymerisable acrylic or methacrylic acid ester-containing compositions
CH611633A5 (fr) *	1977-03-16	1979-06-15	Espe Pharm Praep
DE3471595D1 (en) *	1983-01-20	1988-07-07	Ciba Geigy Ag	Electron-beam curing method for coatings
DE3339485A1 (de) *	1983-10-31	1985-05-15	Wikolin Polymer Chemie Gmbh, 2800 Bremen	Strahlungshaertbare zusammensetzung und verfahren zu ihrer herstellung und verwendung
DE10232828A1 (de) *	2002-07-19	2004-02-05	Goldschmidt Ag	Verwendung von Antioxidantien in strahlenhärtbaren Beschichtungsmassen für die Herstellung von abhäsiven Beschichtungen
US20040087687A1 (en) *	2002-10-30	2004-05-06	Vantico A&T Us Inc.	Photocurable compositions with phosphite viscosity stabilizers
DE102006012274A1 (de) *	2006-03-15	2007-09-20	Votteler Lackfabrik Gmbh & Co. Kg	Lack zur Oberflächenbeschichtung von Formteilen
US7776509B2 (en) *	2007-02-06	2010-08-17	Canon Kabushiki Kaisha	Photosensitive compound, photosensitive composition, resist pattern forming method, and device production process
JP2012530156A (ja) *	2009-06-12	2012-11-29	イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー	放射線硬化性コーティング組成物
EP2440620B1 (fr)	2009-06-12	2014-08-13	Coatings Foreign IP Co. LLC	Procede de revetement multicouche
US8399533B2 (en)	2010-11-15	2013-03-19	Eastman Kodak Company	Photocurable compositions containing N-oxyazinium salt photoinitiators

1971
- 1971-01-29 US US111158A patent/US3699022A/en not_active Expired - Lifetime
- 1971-02-03 DE DE2104958A patent/DE2104958C3/de not_active Expired
- 1971-02-03 FI FI710288A patent/FI50794C/fi active
- 1971-02-03 DE DE19712166601 patent/DE2166601A1/de active Pending
- 1971-02-04 JP JP46004071A patent/JPS515439B1/ja active Pending
- 1971-02-04 FR FR7104924A patent/FR2079275A1/fr not_active Withdrawn
- 1971-02-04 SE SE7101373A patent/SE371447B/xx unknown
- 1971-02-04 BE BE762509A patent/BE762509A/fr unknown
- 1971-02-04 NO NO412/71A patent/NO131842C/no unknown
- 1971-02-05 DK DK50771AA patent/DK135173B/da unknown

Also Published As

Publication number	Publication date
DK135173C (fr)	1977-08-15
NO131842C (fr)	1975-08-13
FI50794C (fi)	1976-07-12
BE762509A (fr)	1971-07-16
SE371447B (fr)	1974-11-18
US3699022A (en)	1972-10-17
DE2104958B2 (de)	1975-05-07
DE2104958A1 (de)	1971-08-19
DE2104958C3 (de)	1976-01-02
DK135173B (da)	1977-03-14
JPS515439B1 (fr)	1976-02-19
FI50794B (fr)	1976-03-31
FR2079275A1 (fr)	1971-11-12
DE2166601A1 (de)	1974-10-10

Publication	Publication Date	Title
NO131842B (fr)	1975-05-05
US8906502B2 (en)	2014-12-09	Organic powder useful as the replacement of mineral filler in composites
BRPI0816808B1 (pt)	2019-04-02	Composição de resina acrílica poliéster termocurável de baixo cov para revestimento em gel
JP3479202B2 (ja)	2003-12-15	光硬化性プリプレグ組成物及びその製造方法
US4353787A (en)	1982-10-12	Photo curable polyester with benzoyl oxime carbonate, photo reducible dye (eosin), and a benzyl amine
EP2808361A1 (fr)	2014-12-03	Composition composite contenant un polyol d'éther polycyclique
US4255464A (en)	1981-03-10	Method for the manufacture of objects from an unsaturated polyester composition
EP0400884A2 (fr)	1990-12-05	Couche de gel à base de polyesters insaturés contenant du 2-méthyl-1,3-propanediol
JP2001294687A (ja)	2001-10-23	硬化性プリプレグ組成物，その製造方法及び硬化方法
US4904536A (en)	1990-02-27	Process for controlling monomeric emissions
SU357732A1 (ru)		ФОТОПОЛИМЕРИЗУЕМЬгй СОСТАВ
DE2259161C3 (de)	1978-08-17	Verfahren zur Herstellung von Formkörpern, Imprägnierungen, Überzügen u.dgl. aus durch UV-Bestrahlung härtbaren Zubereitungen
US4720392A (en)	1988-01-19	Process for controlling monomeric emissions
JPH0977836A (ja)	1997-03-25	光硬化性複合材料組成物
EP1092744B1 (fr)	2006-03-08	Composition de preimpregne thermodurcissable et son procede de production
DE2502218B2 (de)	1977-09-29	Herstellung von nicht vergruenenden formteilen oder ueberzuegen
EP0324040B1 (fr)	1992-07-08	Procédé pour contrôler l'émission de monomères
US2824080A (en)	1958-02-18	Mixtures of hydroxy phenones and esters of salicylic acid in resins as inhibitors of discoloration by light
CH545329A (de)	1974-01-31	Durch UV-Bestrahlung härtbare Zubereitungen auf Grundlage ungesättigter Polyesterharze
Kandelbauer et al.	2013	Handbook of thermoset plastics: 6. Unsaturated polyesters and vinyl esters
CH534705A (de)	1973-03-15	Verfahren zur Herstellung von Formkörpern, Imprägnierungen und Ueberzügen
JPH0131532B2 (fr)	1989-06-27
JPH0220648B2 (fr)	1990-05-10
DE2104972A1 (de)	1971-08-12	Aus Glasseiden gewebe bzw Glas seidenmatte und poly men siertem Poly ester bestehende Laminatbahn
CH573461A5 (en)	1976-03-15	Photochemically polymerisable polyester moulding composn