NO861170L - Fremgangsmaate for stabilisering av polyisocyanatopploesninger. - Google Patents

Fremgangsmaate for stabilisering av polyisocyanatopploesninger.

Info

Publication number: NO861170L
Authority: NO; Norway
Prior art keywords: residue; formula; stands; above meaning; solutions
Prior art date: 1985-05-21

Application number

NO861170A

Other languages

English (en)

Norwegian (no)

Inventor

Jean Robin

Original Assignee

Rhone Poulenc Spec Chim

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.)

1985-05-21

Filing date

1986-03-24

Publication date

1986-11-24

1986-03-24 Application filed by Rhone Poulenc Spec Chim filed Critical Rhone Poulenc Spec Chim

1986-11-24 Publication of NO861170L publication Critical patent/NO861170L/no

Links

239000005056 polyisocyanate Substances 0.000 title claims description 31
229920001228 polyisocyanate Polymers 0.000 title claims description 31
238000000034 method Methods 0.000 title claims description 13
230000000087 stabilizing effect Effects 0.000 title claims description 5
-1 hydrocarbon radical Chemical class 0.000 claims description 22
150000001875 compounds Chemical class 0.000 claims description 18
125000004432 carbon atom Chemical group C* 0.000 claims description 10
239000003960 organic solvent Substances 0.000 claims description 10
230000015572 biosynthetic process Effects 0.000 claims description 9
239000002244 precipitate Substances 0.000 claims description 9
239000002253 acid Substances 0.000 claims description 8
125000000217 alkyl group Chemical group 0.000 claims description 7
IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims description 7
125000000524 functional group Chemical group 0.000 claims description 6
125000005843 halogen group Chemical group 0.000 claims description 6
125000001931 aliphatic group Chemical group 0.000 claims description 5
125000004423 acyloxy group Chemical group 0.000 claims description 4
229920006395 saturated elastomer Polymers 0.000 claims description 4
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 3
239000004215 Carbon black (E152) Substances 0.000 claims description 3
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 3
125000003710 aryl alkyl group Chemical group 0.000 claims description 3
125000003118 aryl group Chemical group 0.000 claims description 3
229910052801 chlorine Inorganic materials 0.000 claims description 3
239000000460 chlorine Substances 0.000 claims description 3
229910052731 fluorine Inorganic materials 0.000 claims description 3
239000011737 fluorine Substances 0.000 claims description 3
229930195733 hydrocarbon Natural products 0.000 claims description 3
150000003254 radicals Chemical class 0.000 claims description 3
150000005840 aryl radicals Chemical class 0.000 claims description 2
239000012948 isocyanate Substances 0.000 claims description 2
150000002513 isocyanates Chemical class 0.000 claims description 2
125000004430 oxygen atom Chemical group O* 0.000 claims description 2
229910052717 sulfur Inorganic materials 0.000 claims description 2
125000004434 sulfur atom Chemical group 0.000 claims description 2
KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 claims 1
125000002029 aromatic hydrocarbon group Chemical group 0.000 claims 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 1
229910052760 oxygen Inorganic materials 0.000 claims 1
239000001301 oxygen Substances 0.000 claims 1
239000000243 solution Substances 0.000 description 16
239000002904 solvent Substances 0.000 description 14
239000000203 mixture Substances 0.000 description 13
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 7
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
238000000576 coating method Methods 0.000 description 6
VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 6
239000011248 coating agent Substances 0.000 description 5
238000006243 chemical reaction Methods 0.000 description 4
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical class OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 4
239000011527 polyurethane coating Substances 0.000 description 4
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 3
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
239000005057 Hexamethylene diisocyanate Substances 0.000 description 3
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 3
229910052739 hydrogen Inorganic materials 0.000 description 3
239000001257 hydrogen Substances 0.000 description 3
229920005862 polyol Polymers 0.000 description 3
150000003077 polyols Chemical class 0.000 description 3
PIILXFBHQILWPS-UHFFFAOYSA-N tributyltin Chemical compound CCCC[Sn](CCCC)CCCC PIILXFBHQILWPS-UHFFFAOYSA-N 0.000 description 3
239000002966 varnish Substances 0.000 description 3
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
229910019142 PO4 Inorganic materials 0.000 description 2
ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical class [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 2
GCTFWCDSFPMHHS-UHFFFAOYSA-M Tributyltin chloride Chemical compound CCCC[Sn](Cl)(CCCC)CCCC GCTFWCDSFPMHHS-UHFFFAOYSA-M 0.000 description 2
150000004945 aromatic hydrocarbons Chemical group 0.000 description 2
OHJMTUPIZMNBFR-UHFFFAOYSA-N biuret Chemical group NC(=O)NC(N)=O OHJMTUPIZMNBFR-UHFFFAOYSA-N 0.000 description 2
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 2
229910052794 bromium Inorganic materials 0.000 description 2
239000003795 chemical substances by application Substances 0.000 description 2
125000000753 cycloalkyl group Chemical group 0.000 description 2
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
238000006006 cyclotrimerization reaction Methods 0.000 description 2
ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical group OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 2
239000003973 paint Substances 0.000 description 2
NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 2
239000010452 phosphate Substances 0.000 description 2
239000004814 polyurethane Substances 0.000 description 2
229920002635 polyurethane Polymers 0.000 description 2
239000000126 substance Substances 0.000 description 2
239000000758 substrate Substances 0.000 description 2
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 2
239000008096 xylene Substances 0.000 description 2
DFPJRUKWEPYFJT-UHFFFAOYSA-N 1,5-diisocyanatopentane Chemical compound O=C=NCCCCCN=C=O DFPJRUKWEPYFJT-UHFFFAOYSA-N 0.000 description 1
QUPKOUOXSNGVLB-UHFFFAOYSA-N 1,8-diisocyanatooctane Chemical compound O=C=NCCCCCCCCN=C=O QUPKOUOXSNGVLB-UHFFFAOYSA-N 0.000 description 1
ZYVYEJXMYBUCMN-UHFFFAOYSA-N 1-methoxy-2-methylpropane Chemical compound COCC(C)C ZYVYEJXMYBUCMN-UHFFFAOYSA-N 0.000 description 1
XXXFZKQPYACQLD-UHFFFAOYSA-N 2-(2-hydroxyethoxy)ethyl acetate Chemical compound CC(=O)OCCOCCO XXXFZKQPYACQLD-UHFFFAOYSA-N 0.000 description 1
HXDLWJWIAHWIKI-UHFFFAOYSA-N 2-hydroxyethyl acetate Chemical compound CC(=O)OCCO HXDLWJWIAHWIKI-UHFFFAOYSA-N 0.000 description 1
RMGHERXMTMUMMV-UHFFFAOYSA-N 2-methoxypropane Chemical compound COC(C)C RMGHERXMTMUMMV-UHFFFAOYSA-N 0.000 description 1
XDFUNRTWHPWCKO-UHFFFAOYSA-N 4,5,9,10-tetrahydropyrene Chemical compound C1CC2=CC=CC3=C2C2=C1C=CC=C2CC3 XDFUNRTWHPWCKO-UHFFFAOYSA-N 0.000 description 1
DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 1
239000005058 Isophorone diisocyanate Substances 0.000 description 1
LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-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
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical group ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 1
ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
239000007983 Tris buffer Substances 0.000 description 1
IPTNXMGXEGQYSY-UHFFFAOYSA-N acetic acid;1-methoxybutan-1-ol Chemical compound CC(O)=O.CCCC(O)OC IPTNXMGXEGQYSY-UHFFFAOYSA-N 0.000 description 1
125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 1
125000002252 acyl group Chemical group 0.000 description 1
125000003545 alkoxy group Chemical group 0.000 description 1
229940072049 amyl acetate Drugs 0.000 description 1
PGMYKACGEOXYJE-UHFFFAOYSA-N anhydrous amyl acetate Natural products CCCCCOC(C)=O PGMYKACGEOXYJE-UHFFFAOYSA-N 0.000 description 1
125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 description 1
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
239000003054 catalyst Substances 0.000 description 1
230000003197 catalytic effect Effects 0.000 description 1
239000004567 concrete Substances 0.000 description 1
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
230000001627 detrimental effect Effects 0.000 description 1
YRKILJAUUWNCOC-UHFFFAOYSA-L dibutyl(dodecylsulfanyl)stannanylium;dodecanoate Chemical compound CCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCS[Sn+](CCCC)CCCC YRKILJAUUWNCOC-UHFFFAOYSA-L 0.000 description 1
LLUOVVKKORNDMP-UHFFFAOYSA-M dibutyl(methoxy)stannanylium;acetate Chemical compound CC([O-])=O.CCCC[Sn+](OC)CCCC LLUOVVKKORNDMP-UHFFFAOYSA-M 0.000 description 1
JGFBRKRYDCGYKD-UHFFFAOYSA-N dibutyl(oxo)tin Chemical compound CCCC[Sn](=O)CCCC JGFBRKRYDCGYKD-UHFFFAOYSA-N 0.000 description 1
125000005442 diisocyanate group Chemical group 0.000 description 1
SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
238000004090 dissolution Methods 0.000 description 1
125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
NJVOZLGKTAPUTQ-UHFFFAOYSA-M fentin chloride Chemical compound C=1C=CC=CC=1[Sn](C=1C=CC=CC=1)(Cl)C1=CC=CC=C1 NJVOZLGKTAPUTQ-UHFFFAOYSA-M 0.000 description 1
150000002334 glycols Chemical class 0.000 description 1
150000008282 halocarbons Chemical class 0.000 description 1
MNWFXJYAOYHMED-UHFFFAOYSA-M heptanoate Chemical compound CCCCCCC([O-])=O MNWFXJYAOYHMED-UHFFFAOYSA-M 0.000 description 1
FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
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 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
239000007788 liquid Substances 0.000 description 1
239000002184 metal Substances 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
150000002739 metals Chemical class 0.000 description 1
KJGLZJQPMKQFIK-UHFFFAOYSA-N methanolate;tributylstannanylium Chemical compound CCCC[Sn](CCCC)(CCCC)OC KJGLZJQPMKQFIK-UHFFFAOYSA-N 0.000 description 1
KZKQGUVWZYKJBN-UHFFFAOYSA-N methyl 5-methylsulfonylpyridine-3-carboxylate Chemical compound COC(=O)C1=CN=CC(S(C)(=O)=O)=C1 KZKQGUVWZYKJBN-UHFFFAOYSA-N 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
125000003136 n-heptyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 1
125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
125000001624 naphthyl group Chemical group 0.000 description 1
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
125000004334 oxygen containing inorganic group Chemical group 0.000 description 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
239000000049 pigment Substances 0.000 description 1
239000004033 plastic Substances 0.000 description 1
229920003023 plastic Polymers 0.000 description 1
229920000728 polyester Polymers 0.000 description 1
229920000570 polyether Polymers 0.000 description 1
229920000582 polyisocyanurate Polymers 0.000 description 1
239000011495 polyisocyanurate Substances 0.000 description 1
125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
230000009257 reactivity Effects 0.000 description 1
230000006641 stabilisation Effects 0.000 description 1
238000011105 stabilization Methods 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
239000002562 thickening agent Substances 0.000 description 1
125000005425 toluyl group Chemical group 0.000 description 1
JNZRDLWZFWFSBK-UHFFFAOYSA-N tribenzyltin Chemical compound C=1C=CC=CC=1C[Sn](CC=1C=CC=CC=1)CC1=CC=CC=C1 JNZRDLWZFWFSBK-UHFFFAOYSA-N 0.000 description 1
BDIWFCKBPZPBQT-UHFFFAOYSA-N tributyl(tributylstannylsulfanyl)stannane Chemical compound CCCC[Sn](CCCC)(CCCC)S[Sn](CCCC)(CCCC)CCCC BDIWFCKBPZPBQT-UHFFFAOYSA-N 0.000 description 1
UBOXGVDOUJQMTN-UHFFFAOYSA-N trichloroethylene Natural products ClCC(Cl)Cl UBOXGVDOUJQMTN-UHFFFAOYSA-N 0.000 description 1
UEUTXOXUEXNSLK-UHFFFAOYSA-M triethyl(2-methylpropylsulfanyl)stannane Chemical compound CC[Sn](CC)(CC)SCC(C)C UEUTXOXUEXNSLK-UHFFFAOYSA-M 0.000 description 1
ULSFLISUZBMBRX-UHFFFAOYSA-M triethylstannyl dodecanoate Chemical compound CC[Sn+](CC)CC.CCCCCCCCCCCC([O-])=O ULSFLISUZBMBRX-UHFFFAOYSA-M 0.000 description 1
CPRPKIMXLHBUGA-UHFFFAOYSA-N triethyltin Chemical compound CC[Sn](CC)CC CPRPKIMXLHBUGA-UHFFFAOYSA-N 0.000 description 1
229940113165 trimethylolpropane Drugs 0.000 description 1
BYVAUQCHMDRWFV-UHFFFAOYSA-M trioctylstannanylium;bromide Chemical compound CCCCCCCC[Sn](Br)(CCCCCCCC)CCCCCCCC BYVAUQCHMDRWFV-UHFFFAOYSA-M 0.000 description 1
NTCQOKPUDSWFJF-UHFFFAOYSA-N triphenyl(triphenylstannylsulfanyl)stannane Chemical compound C=1C=CC=CC=1[Sn](C=1C=CC=CC=1)(C=1C=CC=CC=1)S[Sn](C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 NTCQOKPUDSWFJF-UHFFFAOYSA-N 0.000 description 1
NHSGFFFVCFHOBS-UHFFFAOYSA-M tris(2-methylpropyl)stannanylium;chloride Chemical compound CC(C)C[Sn](Cl)(CC(C)C)CC(C)C NHSGFFFVCFHOBS-UHFFFAOYSA-M 0.000 description 1
YVPMSOFRDQQNMG-UHFFFAOYSA-M tris(4-chlorophenyl)stannanylium;chloride Chemical compound C1=CC(Cl)=CC=C1[Sn](Cl)(C=1C=CC(Cl)=CC=1)C1=CC=C(Cl)C=C1 YVPMSOFRDQQNMG-UHFFFAOYSA-M 0.000 description 1
239000002023 wood Substances 0.000 description 1
150000003738 xylenes Chemical class 0.000 description 1
125000005023 xylyl group Chemical group 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L79/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing nitrogen with or without oxygen or carbon only, not provided for in groups C08L61/00 - C08L77/00
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C265/00—Derivatives of isocyanic acid
- C07C265/14—Derivatives of isocyanic acid containing at least two isocyanate groups bound to the same carbon skeleton
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D251/00—Heterocyclic compounds containing 1,3,5-triazine rings
- C07D251/02—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
- C07D251/12—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D251/26—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with only hetero atoms directly attached to ring carbon atoms
- C07D251/30—Only oxygen atoms
- C07D251/34—Cyanuric or isocyanuric esters
- 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
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Polyurethanes Or Polyureas (AREA)
Liquid Crystal Substances (AREA)
Compositions Of Macromolecular Compounds (AREA)
Paints Or Removers (AREA)

NO861170A 1985-05-21 1986-03-24 Fremgangsmaate for stabilisering av polyisocyanatopploesninger. NO861170L (no)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
FR8507817A FR2582303B1 (fr)	1985-05-21	1985-05-21	Procede de stabilisation de solutions organiques de polyisocyanates

Publications (1)

Publication Number	Publication Date
NO861170L true NO861170L (no)	1986-11-24

Family

ID=9319521

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO861170A NO861170L (no)	1985-05-21	1986-03-24	Fremgangsmaate for stabilisering av polyisocyanatopploesninger.

Country Status (11)

Country	Link
US (1)	US4828753A (de)
EP (1)	EP0203874B1 (de)
JP (1)	JPS61268715A (de)
KR (1)	KR860009076A (de)
AR (1)	AR240331A1 (de)
AT (1)	ATE55112T1 (de)
BR (1)	BR8601950A (de)
CA (1)	CA1252479A (de)
DE (1)	DE3673074D1 (de)
FR (1)	FR2582303B1 (de)
NO (1)	NO861170L (de)

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US5194559A (en) *	1991-03-25	1993-03-16	Mitsui Toatsu Chemicals, Inc.	Optical urethane resins and plastic lenses comprising the same
DE4331085A1 (de) *	1993-09-13	1995-03-16	Basf Ag	Stabile, nach phosgenfreien Verfahren erhältliche Polyisocyanatzusammensetzungen und ein Verfahren zu ihrer Herstellung
DE4331083A1 (de) *	1993-09-13	1995-03-16	Basf Ag	Lagerstabile, nach phosgenfreien Verfahren erhältliche Polyisocyanatzusammensetzungen, ein Verfahren zu ihrer Herstellung und ihre Verwendung
DE19647296A1 (de) *	1996-11-15	1998-05-20	Basf Ag	Zinnhaltige Polyisocyanate und Verfahren zur Herstellung von Polyisocyanat-Polyadditionsprodukten
JP6080857B2 (ja)	2011-10-28	2017-02-15	ビーエーエスエフソシエタス・ヨーロピアＢａｓｆＳｅ	溶剤中で凝集安定性の、（環式）脂肪族ジイソシアナートのポリイソシアナートの製造方法
US9617402B2 (en)	2011-10-28	2017-04-11	Basf Se	Process for preparing polyisocyanates which are flocculation-stable in solvents from (cyclo)aliphatic diisocyanates
EP3305863A1 (de)	2016-10-07	2018-04-11	Basf Se	Verfahren zur herstellung von in lösungsmitteln flockulationsstabilen polyisocyanaten von (cyclo)aliphatischen diisocyanaten
EP3336117A1 (de)	2017-09-20	2018-06-20	Basf Se	Verfahren zur herstellung von in lösungsmitteln flockulationsstabilen polyisocyanaten von (cyclo)aliphatischen diisocyanaten

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US3376230A (en) *	1965-01-08	1968-04-02	Du Pont	Stabilized solutions of ferric chloride in toluene diisocyanate
DE1595256A1 (de) *	1965-02-19	1969-08-21	Allied Chem	Haertbare Urethanmassen
CA1050699A (en) *	1974-12-19	1979-03-13	M And T Chemicals Inc.	Hydrolytically stable urethane foam precursors
DE2552350A1 (de) *	1975-11-21	1977-05-26	Bayer Ag	Lagerstabile, carbodiimidgruppen enthaltende polyisocyanate
JPS5667331A (en) *	1979-11-13	1981-06-06	Sanyo Chem Ind Ltd	Polyol composition
US4286073A (en) *	1980-07-28	1981-08-25	Air Products And Chemicals, Inc.	Urethane catalysis
DE3033330A1 (de) *	1980-09-04	1982-04-29	Bayer Ag, 5090 Leverkusen	Verfahren zur herstellung von fluessigen gemischen von isocyanatgruppen aufweisenden verbindungen, sowie ihre verwendung als aufbaukomponente bei der herstellung von polyurethankunststoffen
JPS57168912A (en) *	1981-04-10	1982-10-18	Mitsubishi Chem Ind Ltd	Urethane prepolymer composition
DE3131780A1 (de) *	1981-08-12	1983-02-24	Bayer Ag, 5090 Leverkusen	Langzeit-lagerbestaendige, heterogene einkomponentensysteme aus polyol-/diphenylmethan-uretdion-diisocyanaten, verfahren zu ihrer herstellung und ihre verwendung zur synthese hochmolekularer polyurethane
DE3204128A1 (de) *	1982-02-06	1983-08-11	Bayer Ag, 5090 Leverkusen	Verwendung von isocyanato-silanen als die lagerstabilitaet erhoehende zusatzmittel in, polyurethanprepolymere mit freien isocyanatgruppen aufweisenden, zubereitungen
DE3343124A1 (de) *	1983-11-29	1985-06-05	Basf Ag, 6700 Ludwigshafen	Bei raumtemperatur lagerstabile, durch hitzeeinwirkung haertbare stoffmischungen auf basis von verbindungen mit reaktiven wasserstoffatomen und polyisocyanaten, verfahren zu ihrer herstellung und ihre verwendung zur herstellung von formteilen
US4595712A (en) *	1985-01-22	1986-06-17	Societe Chimique Des Charbonnages, S.A.	Stable prepolymers of polyisocyanate with hydroxyl functions, a process for their manufacture and their application to the manufacture of polyurethanes

1985
- 1985-05-21 FR FR8507817A patent/FR2582303B1/fr not_active Expired
1986
- 1986-03-24 NO NO861170A patent/NO861170L/no unknown
- 1986-04-03 CA CA000505782A patent/CA1252479A/fr not_active Expired
- 1986-04-30 BR BR8601950A patent/BR8601950A/pt unknown
- 1986-05-15 AT AT86420123T patent/ATE55112T1/de not_active IP Right Cessation
- 1986-05-15 DE DE8686420123T patent/DE3673074D1/de not_active Expired - Fee Related
- 1986-05-15 EP EP86420123A patent/EP0203874B1/de not_active Expired - Lifetime
- 1986-05-19 JP JP61112838A patent/JPS61268715A/ja active Pending
- 1986-05-20 AR AR304013A patent/AR240331A1/es active
- 1986-05-20 KR KR1019860003907A patent/KR860009076A/ko not_active Ceased
- 1986-05-21 US US06/865,420 patent/US4828753A/en not_active Expired - Fee Related

Also Published As

Publication number	Publication date
US4828753A (en)	1989-05-09
FR2582303A1 (fr)	1986-11-28
JPS61268715A (ja)	1986-11-28
CA1252479A (fr)	1989-04-11
KR860009076A (ko)	1986-12-20
BR8601950A (pt)	1987-01-06
FR2582303B1 (fr)	1987-07-10
EP0203874B1 (de)	1990-08-01
ATE55112T1 (de)	1990-08-15
EP0203874A1 (de)	1986-12-03
DE3673074D1 (de)	1990-09-06
AR240331A1 (es)	1990-03-30

Publication	Publication Date	Title
CA1334848C (en)	1995-03-21	Process for the production of polyisocyanates which contain isocyanurate groups
US4014935A (en)	1977-03-29	Carbodiimides
KR100453869B1 (ko)	2004-12-30	이미노옥사디아진디온기를함유하는이소시아네이트삼량체,그의제조방법및용도
US4614785A (en)	1986-09-30	Process for the production of oligomeric polyisocyanates and their use in the production of polyurethane plastics
US4888442A (en)	1989-12-19	Reduction of free monomer in isocyanate adducts
US4912210A (en)	1990-03-27	Process for the preparation of (cyclo)aliphatic uretediones
US5237058A (en)	1993-08-17	Polyisocyanates containing uretdione and/or isocyanurate groups, a process for their production
US4085140A (en)	1978-04-18	Carbodiimides
CA2093884A1 (en)	1993-12-13	Polyisocyanates containing allophanate and isocyanurate groups, a process for their production from a mixture of diisocyanates and their use in two-component coating compositions
CA2125237A1 (en)	1994-12-23	Polyisocyanates containing allophanate and isocyanurate groups, a process for their production from cyclic diisocyanates and their use in two-component coating compositions
KR20040004130A (ko)	2004-01-13	단량체 함량이 낮은 ｔｄｉ 삼량체의 제조 방법
ES2329016T3 (es)	2009-11-20	Procedimiento para la preparacion de poliisocianatos alifaticos con estructura uretodiona, isocianurato asi como iminooxadiazindiona.
US6765111B1 (en)	2004-07-20	Process for the production of polyisocyanates containing isocyanurate groups and their use
CN101450928B (zh)	2014-01-29	脲二酮聚异氰酸酯的制备
US20030135007A1 (en)	2003-07-17	Catalysts for preparing polyisocyanates containing isocyanurate groups, and their use
US4828753A (en)	1989-05-09	Storage-stable organic solutions of polyisocyanates
EP0105242B1 (de)	1987-06-16	Reduktion von freiem Monomer in Isocyanat-Additionsprodukten
US5798431A (en)	1998-08-25	Process for the production of polyisocyanates containing isocyanurate groups from aliphatic and aromatic isocyanate compounds
US3330849A (en)	1967-07-11	Stabilization of organic isocyanates
US3960950A (en)	1976-06-01	Process for carbodiiomide synthesis
JP4235274B2 (ja)	2009-03-11	（シクロ）脂肪族１，４−ジイソシアネートからの多環式イミノオキサジアジンジオン
EP0077105B1 (de)	1985-08-14	Diisocyanate
US3267137A (en)	1966-08-16	Process for the manufacture of polycarbodhmides
US3641024A (en)	1972-02-08	Low molecular weight polyisocyanates
US6391161B1 (en)	2002-05-21	Method for reducing the chlorine content of low molecular weight isocyanates