NO852888L - Fremgangsmaate ved fremstilling av kunstharpiksmasser som er lagerstabilt uten utelukkelse av fuktighet, og anvendelse derav. - Google Patents

Fremgangsmaate ved fremstilling av kunstharpiksmasser som er lagerstabilt uten utelukkelse av fuktighet, og anvendelse derav.

Info

Publication number: NO852888L
Authority: NO; Norway
Prior art keywords: diisocyanate; prepolymeric; silanes; cycloaliphatic; approx
Prior art date: 1984-07-21

Application number

NO852888A

Other languages

English (en)

Norwegian (no)

Inventor

Bernd Brinkmann

Hermann-Josef Lucas

Original Assignee

Schering 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.)

1984-07-21

Filing date

1985-07-19

Publication date

1986-01-22

1985-07-19 Application filed by Schering Ag filed Critical Schering Ag

1986-01-22 Publication of NO852888L publication Critical patent/NO852888L/no

Links

230000007717 exclusion Effects 0.000 title claims abstract description 4
238000000034 method Methods 0.000 title claims description 12
238000004519 manufacturing process Methods 0.000 title claims description 7
238000007789 sealing Methods 0.000 claims abstract description 13
239000000853 adhesive Substances 0.000 claims abstract description 7
230000001070 adhesive effect Effects 0.000 claims abstract description 7
239000011248 coating agent Substances 0.000 claims abstract description 6
238000000576 coating method Methods 0.000 claims abstract description 6
239000012948 isocyanate Substances 0.000 claims description 17
150000002513 isocyanates Chemical class 0.000 claims description 17
150000001875 compounds Chemical class 0.000 claims description 15
150000004756 silanes Chemical class 0.000 claims description 12
125000004432 carbon atom Chemical group C* 0.000 claims description 9
239000007795 chemical reaction product Substances 0.000 claims description 7
229920003002 synthetic resin Polymers 0.000 claims description 7
239000000057 synthetic resin Substances 0.000 claims description 7
150000001298 alcohols Chemical class 0.000 claims description 6
239000005058 Isophorone diisocyanate Substances 0.000 claims description 3
125000001931 aliphatic group Chemical group 0.000 claims description 3
RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 claims 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 claims description 3
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 3
229920001451 polypropylene glycol Polymers 0.000 claims description 3
239000000654 additive Substances 0.000 claims description 2
125000000217 alkyl group Chemical group 0.000 claims description 2
125000002029 aromatic hydrocarbon group Chemical group 0.000 claims description 2
125000003118 aryl group Chemical group 0.000 claims description 2
125000000547 substituted alkyl group Chemical group 0.000 claims description 2
VZXPHDGHQXLXJC-UHFFFAOYSA-N 1,6-diisocyanato-5,6-dimethylheptane Chemical compound O=C=NC(C)(C)C(C)CCCCN=C=O VZXPHDGHQXLXJC-UHFFFAOYSA-N 0.000 claims 1
239000005057 Hexamethylene diisocyanate Substances 0.000 claims 1
JXCHMDATRWUOAP-UHFFFAOYSA-N diisocyanatomethylbenzene Chemical compound O=C=NC(N=C=O)C1=CC=CC=C1 JXCHMDATRWUOAP-UHFFFAOYSA-N 0.000 claims 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
239000000203 mixture Substances 0.000 abstract description 9
239000004721 Polyphenylene oxide Substances 0.000 abstract description 5
229920000570 polyether Polymers 0.000 abstract description 5
150000003673 urethanes Chemical class 0.000 abstract description 3
125000003545 alkoxy group Chemical group 0.000 abstract 1
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
125000003396 thiol group Chemical group [H]S* 0.000 abstract 1
239000000047 product Substances 0.000 description 13
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 9
229920005862 polyol Polymers 0.000 description 9
150000003077 polyols Chemical class 0.000 description 9
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 8
238000006243 chemical reaction Methods 0.000 description 8
238000006068 polycondensation reaction Methods 0.000 description 8
-1 amino- Chemical class 0.000 description 7
239000005056 polyisocyanate Substances 0.000 description 7
229920001228 polyisocyanate Polymers 0.000 description 7
PJANXHGTPQOBST-VAWYXSNFSA-N trans-stilbene Chemical group C=1C=CC=CC=1/C=C/C1=CC=CC=C1 PJANXHGTPQOBST-VAWYXSNFSA-N 0.000 description 7
238000006116 polymerization reaction Methods 0.000 description 6
239000003054 catalyst Substances 0.000 description 5
IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 5
235000011007 phosphoric acid Nutrition 0.000 description 5
239000002904 solvent Substances 0.000 description 5
SBASXUCJHJRPEV-UHFFFAOYSA-N 2-(2-methoxyethoxy)ethanol Chemical compound COCCOCCO SBASXUCJHJRPEV-UHFFFAOYSA-N 0.000 description 4
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 4
230000002745 absorbent Effects 0.000 description 4
239000002250 absorbent Substances 0.000 description 4
229910000147 aluminium phosphate Inorganic materials 0.000 description 4
150000001412 amines Chemical class 0.000 description 4
230000015572 biosynthetic process Effects 0.000 description 4
238000004821 distillation Methods 0.000 description 4
NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 4
XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 4
229910052751 metal Inorganic materials 0.000 description 4
239000002184 metal Substances 0.000 description 4
JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 4
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
239000004970 Chain extender Substances 0.000 description 3
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 3
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 3
BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 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
239000012975 dibutyltin dilaurate Substances 0.000 description 3
238000002360 preparation method Methods 0.000 description 3
239000011541 reaction mixture Substances 0.000 description 3
238000010992 reflux Methods 0.000 description 3
229910000077 silane Inorganic materials 0.000 description 3
ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 3
229940008841 1,6-hexamethylene diisocyanate Drugs 0.000 description 2
SJECZPVISLOESU-UHFFFAOYSA-N 3-trimethoxysilylpropan-1-amine Chemical compound CO[Si](OC)(OC)CCCN SJECZPVISLOESU-UHFFFAOYSA-N 0.000 description 2
KZMGYPLQYOPHEL-UHFFFAOYSA-N Boron trifluoride etherate Chemical compound FB(F)F.CCOCC KZMGYPLQYOPHEL-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
RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 2
BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 2
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-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
239000003377 acid catalyst Substances 0.000 description 2
230000002378 acidificating 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
HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 description 2
239000003795 chemical substances by application Substances 0.000 description 2
238000010276 construction Methods 0.000 description 2
238000001816 cooling Methods 0.000 description 2
238000007334 copolymerization reaction Methods 0.000 description 2
238000004132 cross linking Methods 0.000 description 2
MWKFXSUHUHTGQN-UHFFFAOYSA-N decan-1-ol Chemical compound CCCCCCCCCCO MWKFXSUHUHTGQN-UHFFFAOYSA-N 0.000 description 2
150000002009 diols Chemical class 0.000 description 2
LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 2
238000006266 etherification reaction Methods 0.000 description 2
239000000945 filler Substances 0.000 description 2
ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 description 2
GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 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
239000000758 substrate Substances 0.000 description 2
TXDNPSYEJHXKMK-UHFFFAOYSA-N sulfanylsilane Chemical class S[SiH3] TXDNPSYEJHXKMK-UHFFFAOYSA-N 0.000 description 2
ZWVMLYRJXORSEP-UHFFFAOYSA-N 1,2,6-Hexanetriol Chemical compound OCCCCC(O)CO ZWVMLYRJXORSEP-UHFFFAOYSA-N 0.000 description 1
RTTZISZSHSCFRH-UHFFFAOYSA-N 1,3-bis(isocyanatomethyl)benzene Chemical compound O=C=NCC1=CC=CC(CN=C=O)=C1 RTTZISZSHSCFRH-UHFFFAOYSA-N 0.000 description 1
QGLRLXLDMZCFBP-UHFFFAOYSA-N 1,6-diisocyanato-2,4,4-trimethylhexane Chemical compound O=C=NCC(C)CC(C)(C)CCN=C=O QGLRLXLDMZCFBP-UHFFFAOYSA-N 0.000 description 1
NFDXQGNDWIPXQL-UHFFFAOYSA-N 1-cyclooctyldiazocane Chemical compound C1CCCCCCC1N1NCCCCCC1 NFDXQGNDWIPXQL-UHFFFAOYSA-N 0.000 description 1
IUVCFHHAEHNCFT-INIZCTEOSA-N 2-[(1s)-1-[4-amino-3-(3-fluoro-4-propan-2-yloxyphenyl)pyrazolo[3,4-d]pyrimidin-1-yl]ethyl]-6-fluoro-3-(3-fluorophenyl)chromen-4-one Chemical compound C1=C(F)C(OC(C)C)=CC=C1C(C1=C(N)N=CN=C11)=NN1[C@@H](C)C1=C(C=2C=C(F)C=CC=2)C(=O)C2=CC(F)=CC=C2O1 IUVCFHHAEHNCFT-INIZCTEOSA-N 0.000 description 1
FYGFQAJDFJYPLK-UHFFFAOYSA-N 3-butyloxiran-2-one Chemical compound CCCCC1OC1=O FYGFQAJDFJYPLK-UHFFFAOYSA-N 0.000 description 1
CKPKHTKLLYPGFM-UHFFFAOYSA-N 6,6-dimethylheptane-1,1-diol Chemical class CC(CCCCC(O)O)(C)C CKPKHTKLLYPGFM-UHFFFAOYSA-N 0.000 description 1
DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
MHZGKXUYDGKKIU-UHFFFAOYSA-N Decylamine Chemical compound CCCCCCCCCCN MHZGKXUYDGKKIU-UHFFFAOYSA-N 0.000 description 1
PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-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
229920001730 Moisture cure polyurethane Polymers 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
REYJJPSVUYRZGE-UHFFFAOYSA-N Octadecylamine Chemical compound CCCCCCCCCCCCCCCCCCN REYJJPSVUYRZGE-UHFFFAOYSA-N 0.000 description 1
239000004952 Polyamide Substances 0.000 description 1
AWMVMTVKBNGEAK-UHFFFAOYSA-N Styrene oxide Chemical compound C1OC1C1=CC=CC=C1 AWMVMTVKBNGEAK-UHFFFAOYSA-N 0.000 description 1
ISKQADXMHQSTHK-UHFFFAOYSA-N [4-(aminomethyl)phenyl]methanamine Chemical compound NCC1=CC=C(CN)C=C1 ISKQADXMHQSTHK-UHFFFAOYSA-N 0.000 description 1
239000002253 acid Substances 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
239000002318 adhesion promoter Substances 0.000 description 1
239000013466 adhesive and sealant Substances 0.000 description 1
238000004026 adhesive bonding Methods 0.000 description 1
239000001361 adipic acid Substances 0.000 description 1
235000011037 adipic acid Nutrition 0.000 description 1
125000005370 alkoxysilyl group Chemical group 0.000 description 1
125000002947 alkylene group Chemical group 0.000 description 1
150000001414 amino alcohols Chemical class 0.000 description 1
238000010539 anionic addition polymerization reaction Methods 0.000 description 1
239000003963 antioxidant agent Substances 0.000 description 1
HIFVAOIJYDXIJG-UHFFFAOYSA-N benzylbenzene;isocyanic acid Chemical class N=C=O.N=C=O.C=1C=CC=CC=1CC1=CC=CC=C1 HIFVAOIJYDXIJG-UHFFFAOYSA-N 0.000 description 1
238000012661 block copolymerization Methods 0.000 description 1
238000009835 boiling Methods 0.000 description 1
CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 description 1
229910000019 calcium carbonate Inorganic materials 0.000 description 1
239000001110 calcium chloride Substances 0.000 description 1
229910001628 calcium chloride Inorganic materials 0.000 description 1
239000004202 carbamide Substances 0.000 description 1
VPKDCDLSJZCGKE-UHFFFAOYSA-N carbodiimide group Chemical group N=C=N VPKDCDLSJZCGKE-UHFFFAOYSA-N 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
238000010538 cationic polymerization reaction Methods 0.000 description 1
238000003776 cleavage reaction Methods 0.000 description 1
239000007859 condensation product Substances 0.000 description 1
239000012043 crude product Substances 0.000 description 1
150000004292 cyclic ethers Chemical class 0.000 description 1
IFDVQVHZEKPUSC-UHFFFAOYSA-N cyclohex-3-ene-1,2-dicarboxylic acid Chemical compound OC(=O)C1CCC=CC1C(O)=O IFDVQVHZEKPUSC-UHFFFAOYSA-N 0.000 description 1
QSAWQNUELGIYBC-UHFFFAOYSA-N cyclohexane-1,2-dicarboxylic acid Chemical compound OC(=O)C1CCCCC1C(O)=O QSAWQNUELGIYBC-UHFFFAOYSA-N 0.000 description 1
230000001419 dependent effect Effects 0.000 description 1
JQZRVMZHTADUSY-UHFFFAOYSA-L di(octanoyloxy)tin Chemical compound [Sn+2].CCCCCCCC([O-])=O.CCCCCCCC([O-])=O JQZRVMZHTADUSY-UHFFFAOYSA-L 0.000 description 1
239000012973 diazabicyclooctane Substances 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
125000005442 diisocyanate group Chemical group 0.000 description 1
239000000539 dimer Substances 0.000 description 1
CZZYITDELCSZES-UHFFFAOYSA-N diphenylmethane Chemical compound C=1C=CC=CC=1CC1=CC=CC=C1 CZZYITDELCSZES-UHFFFAOYSA-N 0.000 description 1
125000006840 diphenylmethane group Chemical group 0.000 description 1
JRBPAEWTRLWTQC-UHFFFAOYSA-N dodecylamine Chemical compound CCCCCCCCCCCCN JRBPAEWTRLWTQC-UHFFFAOYSA-N 0.000 description 1
239000000428 dust Substances 0.000 description 1
239000000975 dye Substances 0.000 description 1
230000000694 effects Effects 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
125000000524 functional group Chemical group 0.000 description 1
238000004817 gas chromatography Methods 0.000 description 1
150000002334 glycols Chemical class 0.000 description 1
ACCCMOQWYVYDOT-UHFFFAOYSA-N hexane-1,1-diol Chemical compound CCCCCC(O)O ACCCMOQWYVYDOT-UHFFFAOYSA-N 0.000 description 1
FUZZWVXGSFPDMH-UHFFFAOYSA-M hexanoate Chemical compound CCCCCC([O-])=O FUZZWVXGSFPDMH-UHFFFAOYSA-M 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
150000002484 inorganic compounds Chemical class 0.000 description 1
229910010272 inorganic material Inorganic materials 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
239000007788 liquid Substances 0.000 description 1
238000004949 mass spectrometry Methods 0.000 description 1
235000012054 meals Nutrition 0.000 description 1
VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical group C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
ZETYUTMSJWMKNQ-UHFFFAOYSA-N n,n',n'-trimethylhexane-1,6-diamine Chemical compound CNCCCCCCN(C)C ZETYUTMSJWMKNQ-UHFFFAOYSA-N 0.000 description 1
GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 1
SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
150000002894 organic compounds Chemical class 0.000 description 1
239000002245 particle Substances 0.000 description 1
WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
150000003016 phosphoric acids Chemical class 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
229920002647 polyamide Polymers 0.000 description 1
239000004417 polycarbonate Substances 0.000 description 1
229920000515 polycarbonate Polymers 0.000 description 1
229920005906 polyester polyol Polymers 0.000 description 1
229920006149 polyester-amide block copolymer Polymers 0.000 description 1
229920000098 polyolefin Polymers 0.000 description 1
229920006324 polyoxymethylene Polymers 0.000 description 1
229920001296 polysiloxane Polymers 0.000 description 1
229920006295 polythiol Polymers 0.000 description 1
239000004814 polyurethane Substances 0.000 description 1
229920002635 polyurethane Polymers 0.000 description 1
229920000915 polyvinyl chloride Polymers 0.000 description 1
239000011435 rock Substances 0.000 description 1
239000004576 sand Substances 0.000 description 1
230000007017 scission Effects 0.000 description 1
239000005394 sealing glass Substances 0.000 description 1
125000005624 silicic acid group Chemical class 0.000 description 1
235000012239 silicon dioxide Nutrition 0.000 description 1
239000007787 solid Substances 0.000 description 1
238000000638 solvent extraction Methods 0.000 description 1
239000000600 sorbitol Substances 0.000 description 1
238000003756 stirring Methods 0.000 description 1
239000011269 tar Substances 0.000 description 1
239000011271 tar pitch Substances 0.000 description 1
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
UFDHBDMSHIXOKF-UHFFFAOYSA-N tetrahydrophthalic acid Natural products OC(=O)C1=C(C(O)=O)CCCC1 UFDHBDMSHIXOKF-UHFFFAOYSA-N 0.000 description 1
239000002562 thickening agent Substances 0.000 description 1
YODZTKMDCQEPHD-UHFFFAOYSA-N thiodiglycol Chemical compound OCCSCCO YODZTKMDCQEPHD-UHFFFAOYSA-N 0.000 description 1
229950006389 thiodiglycol Drugs 0.000 description 1
238000005809 transesterification reaction Methods 0.000 description 1
238000005829 trimerization reaction Methods 0.000 description 1
QXJQHYBHAIHNGG-UHFFFAOYSA-N trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-UHFFFAOYSA-N 0.000 description 1
JOYRKODLDBILNP-UHFFFAOYSA-N urethane group Chemical group NC(=O)OCC JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
239000008096 xylene Substances 0.000 description 1
DGVVWUTYPXICAM-UHFFFAOYSA-N β‐Mercaptoethanol Chemical compound OCCS DGVVWUTYPXICAM-UHFFFAOYSA-N 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/08—Processes
- C08G18/10—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S528/00—Synthetic resins or natural rubbers -- part of the class 520 series
- Y10S528/901—Room temperature curable silicon-containing polymer

Landscapes

Chemical & Material Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Polyurethanes Or Polyureas (AREA)
Glass Compositions (AREA)
Drying Of Gases (AREA)
Solid-Sorbent Or Filter-Aiding Compositions (AREA)
Compositions Of Macromolecular Compounds (AREA)
Silicon Polymers (AREA)
Prostheses (AREA)
Processes Of Treating Macromolecular Substances (AREA)
Paints Or Removers (AREA)
Diaphragms For Electromechanical Transducers (AREA)
Sealing Material Composition (AREA)
Adhesives Or Adhesive Processes (AREA)

NO852888A 1984-07-21 1985-07-19 Fremgangsmaate ved fremstilling av kunstharpiksmasser som er lagerstabilt uten utelukkelse av fuktighet, og anvendelse derav. NO852888L (no)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19843426987 DE3426987A1 (de)	1984-07-21	1984-07-21	Verfahren zur herstellung von unter feuchtigkeitsausschluss lagerstabilen kunstharzmassen und deren verwendung

Publications (1)

Publication Number	Publication Date
NO852888L true NO852888L (no)	1986-01-22

Family

ID=6241256

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO852888A NO852888L (no)	1984-07-21	1985-07-19	Fremgangsmaate ved fremstilling av kunstharpiksmasser som er lagerstabilt uten utelukkelse av fuktighet, og anvendelse derav.

Country Status (10)

Country	Link
US (1)	US4798878A (es)
EP (1)	EP0170865B1 (es)
JP (1)	JPS6157616A (es)
AT (1)	ATE44962T1 (es)
AU (1)	AU586979B2 (es)
CA (1)	CA1254340A (es)
DE (2)	DE3426987A1 (es)
DK (1)	DK300785A (es)
ES (1)	ES8604277A1 (es)
NO (1)	NO852888L (es)

Families Citing this family (50)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE3629237A1 (de) *	1986-08-28	1988-03-03	Henkel Kgaa	Alkoxysilanterminierte, feuchtigkeitshaertende polyurethane sowie ihre verwendung fuer klebe- und dichtungsmassen
DE3636974A1 (de) *	1986-10-30	1988-05-05	Bayer Ag	Poly-(ether-urethan-harnstoff)polyadditionsprodukte, ihre herstellung, abmischung enthaltend diese sowie ihre verwendung als abformmassen
JPH0674315B2 (ja) *	1986-12-10	1994-09-21	東レチオコール株式会社	一液硬化型組成物
JPS63245485A (ja) *	1987-03-31	1988-10-12	Sanyo Chem Ind Ltd	陶管シ−ル用プライマ−
DE3742661A1 (de) *	1987-12-16	1989-07-13	Hawera Probst Kg Hartmetall	Gesteinsbohrer
JPH024891A (ja) *	1988-06-21	1990-01-09	Mitsubishi Rayon Co Ltd	歯科用接着剤組成物
US5525654A (en) *	1990-09-18	1996-06-11	Henkel Kommanditgesellschaft Auf Aktien	Polyurethane-based sealing and adhesive compositions containing special diurethane plasticizers
DE4029504A1 (de) *	1990-09-18	1992-03-19	Henkel Kgaa	Dichtungs- und klebemassen mit speziellen weichmachern
DE4029505A1 (de) *	1990-09-18	1992-03-19	Henkel Kgaa	Feuchtigkeitshaertende, alkoxysilanterminierte polyurethane
GB9210653D0 (en) *	1992-05-19	1992-07-01	Ici Plc	Silane functional oligomer
US5443903A (en) *	1993-02-25	1995-08-22	Minnesota Mining And Manufacturing Company	Hot melt stick
DE4307024A1 (de) *	1993-03-05	1994-09-08	Muehlbauer Ernst Kg	Kunststoffe mit einem Gehalt an Silan-, Ether-, Urethan- und Harnstoffgruppen
CA2232588A1 (en) *	1995-09-26	1997-04-03	Ameron International Corporation	Polysiloxane polyurethane compositions
US5539045A (en) *	1995-10-27	1996-07-23	Morton International, Inc.	Aliphatic silylated polyurethane mixtures having reduced viscosites
US5840800A (en)	1995-11-02	1998-11-24	Dow Corning Corporation	Crosslinked emulsions of pre-formed silicon modified organic polymers
DE19908562A1 (de)	1998-03-25	1999-10-07	Henkel Kgaa	Polyurethan und polyurethanhaltige Zubereitung
US6329488B1 (en)	1998-11-10	2001-12-11	C. R. Bard, Inc.	Silane copolymer coatings
US6596401B1 (en)	1998-11-10	2003-07-22	C. R. Bard Inc.	Silane copolymer compositions containing active agents
GB9902856D0 (en)	1999-02-10	1999-03-31	Dow Corning	Organosiloxane compositions
US6197912B1 (en) *	1999-08-20	2001-03-06	Ck Witco Corporation	Silane endcapped moisture curable compositions
DE10013628A1 (de)	2000-03-18	2001-09-20	Degussa	Stabile 1:1-Monoaddukte aus sekundären Aminoalkylalkoxysilanen und Diisocyanaten sowie ein Verfahren zu ihrer Herstellung
US6498210B1 (en) *	2000-07-13	2002-12-24	Adco Products, Inc.	Silylated polyurethanes for adhesives and sealants with improved mechanical properties
ES2254847T3 (es)	2001-08-06	2006-06-16	Degussa Ag	Compuestos de organosilicio.
US6803412B2 (en) *	2003-03-13	2004-10-12	H.B. Fuller Licensing & Financing Inc.	Moisture curable hot melt sealants for glass constructions
US20050250871A1 (en) *	2004-02-13	2005-11-10	Alexander Bublewitz	Dental material based on alkoxysilyl-functional polyethers containing a salt of a strong acid as catalyst
US7482420B2 (en)	2004-03-24	2009-01-27	Construction Research & Technology Gmbh	Silane-terminated polyurethanes with high strength and high elongation
DE102004030737A1 (de) *	2004-06-25	2006-01-12	Degussa Ag	Verfahren und Vorrichtung zur Extraktion von Stoffen aus silanmodifizierten Füllstoffen
US7888425B2 (en) *	2004-07-16	2011-02-15	Reichhold, Inc.	Low volatile organic compound stable solvent-based polyurethane compositions for coatings
DE102004045358B4 (de)	2004-09-17	2009-11-26	Kettenbach Gmbh & Co. Kg	Kondensationsvernetzendes Zweikomponenten-Dentalabformmaterial auf Basis von alkoxysilyl- und hydroxylsilylfunktionellen Polyethern
DE102004045214B4 (de)	2004-09-17	2010-01-28	Kettenbach Gmbh & Co. Kg	Zweikomponenten-Dentalabformmaterial auf Basis von hydroxylfunktionellen Polyethern und Alkoxysilanen und/oder Kieselsäureestern
DE102004055450A1 (de) *	2004-11-17	2006-05-18	Degussa Ag	Feuchtigkeitshärtendes Bindemittel
DE102005057801A1 (de)	2005-01-20	2006-08-03	Degussa Ag	Mercaptosilane
DE102005020535B3 (de)	2005-05-03	2006-06-08	Degussa Ag	Verfahren zur Herstellung von Mercaptoorganyl(alkoxysilanen)
DE102005031201A1 (de)	2005-07-01	2007-01-25	Kettenbach Gmbh & Co. Kg	Zu formstabilen Formkörpern aushärtendes kondensationsvernetzendes Dentalmaterial
DE102005038791A1 (de)	2005-08-17	2007-02-22	Degussa Ag	Organosiliciumverbindungen, ihre Herstellung und ihre Verwendung
DE102005060122A1 (de) *	2005-12-16	2007-06-21	Degussa Gmbh	Verfahren zur Herstellung von (Mercaptoorganyl)alkylpolyethersilanen
US8580361B2 (en) *	2006-02-01	2013-11-12	Momentive Performance Materials Inc.	Insulated glass unit with sealant composition having reduced permeability to gas
US20070179236A1 (en) *	2006-02-01	2007-08-02	Landon Shayne J	Sealant composition having reduced permeability to gas
US7541076B2 (en) *	2006-02-01	2009-06-02	Momentive Performance Materials Inc.	Insulated glass unit with sealant composition having reduced permeability to gas
US20070178256A1 (en) *	2006-02-01	2007-08-02	Landon Shayne J	Insulated glass unit with sealant composition having reduced permeability to gas
US7569653B2 (en) *	2006-02-01	2009-08-04	Momentive Performance Materials Inc.	Sealant composition having reduced permeability to gas
DE102006027235A1 (de)	2006-06-09	2008-01-17	Evonik Degussa Gmbh	Kautschukmischungen
DE102006048041A1 (de)	2006-10-09	2008-04-10	Henkel Kgaa	Zusammensetzungen aus teilweise silylterminierten Polymeren
DE102006055739A1 (de) *	2006-11-25	2008-05-29	Bayer Materialscience Ag	Abformmassen
DE102007037556A1 (de)	2007-08-09	2009-02-12	Evonik Degussa Gmbh	Verfahren zur Herstellung von alkylpolyethersubstituierten Mercaptosilanen
DE102009057597A1 (de) *	2009-12-09	2011-06-16	Bayer Materialscience Ag	Polyrethan-Prepolymere
JP5873083B2 (ja) *	2010-06-30	2016-03-01	ダウグローバルテクノロジーズエルエルシー	低粘度シリル変性ポリマー
DE102012223422A1 (de)	2012-12-17	2014-06-18	Henkel Ag & Co. Kgaa	Niedermodulige silanterminierte PU-Präpolymere
JP6255770B2 (ja) *	2013-07-26	2018-01-10	セメダイン株式会社	釉薬付タイル用ウレタン目地材
EP3715397A1 (de) *	2019-03-26	2020-09-30	PolyU GmbH	Zusammensetzung und verfahren zur herstellung feuchtigkeitsvernetzender polymere und deren verwendung

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE1745526B2 (de) *	1967-03-16	1980-04-10	Union Carbide Corp., New York, N.Y. (V.St.A.)	Verfahren zur Herstellung vulkanisierbarer, unter wasserfreien Bedingungen beständiger Polymerisate
DE3220865C2 (de) *	1982-06-03	1984-08-02	Dynamit Nobel Ag, 5210 Troisdorf	Haftkleber auf der Basis von hydroxylgruppenhaltigen Polymermischungen
DE3220866A1 (de) *	1982-06-03	1983-12-08	Dynamit Nobel Ag, 5210 Troisdorf	Vernetzbare harzmischungen
JPS6055022A (ja) *	1983-09-07	1985-03-29	Sunstar Giken Kk	ポリウレタン樹脂組成物
US4590224A (en) *	1984-08-20	1986-05-20	The Dow Chemical Company	Siloxane-containing polyisocyanurate

1984
- 1984-07-21 DE DE19843426987 patent/DE3426987A1/de not_active Withdrawn
1985
- 1985-06-25 ES ES544540A patent/ES8604277A1/es not_active Expired
- 1985-06-28 DE DE8585108007T patent/DE3571819D1/de not_active Expired
- 1985-06-28 EP EP85108007A patent/EP0170865B1/de not_active Expired
- 1985-06-28 AT AT85108007T patent/ATE44962T1/de not_active IP Right Cessation
- 1985-07-02 DK DK300785A patent/DK300785A/da not_active Application Discontinuation
- 1985-07-17 CA CA000486943A patent/CA1254340A/en not_active Expired
- 1985-07-18 AU AU45222/85A patent/AU586979B2/en not_active Ceased
- 1985-07-18 JP JP60157119A patent/JPS6157616A/ja active Pending
- 1985-07-19 NO NO852888A patent/NO852888L/no unknown
- 1985-07-19 US US06/756,626 patent/US4798878A/en not_active Expired - Fee Related

Also Published As

Publication number	Publication date
DE3426987A1 (de)	1986-01-30
US4798878A (en)	1989-01-17
JPS6157616A (ja)	1986-03-24
EP0170865A1 (de)	1986-02-12
AU4522285A (en)	1986-01-23
EP0170865B1 (de)	1989-07-26
ATE44962T1 (de)	1989-08-15
ES8604277A1 (es)	1986-02-01
ES544540A0 (es)	1986-02-01
DK300785A (da)	1986-01-22
AU586979B2 (en)	1989-08-03
DK300785D0 (da)	1985-07-02
CA1254340A (en)	1989-05-16
DE3571819D1 (en)	1989-08-31

Publication	Publication Date	Title
NO852888L (no)	1986-01-22	Fremgangsmaate ved fremstilling av kunstharpiksmasser som er lagerstabilt uten utelukkelse av fuktighet, og anvendelse derav.
FI74988C (fi)	1988-04-11	Elastiska konsthartsmassor pao basis av polyuretan med oxialkylgrupphaltiga silaner och anvaendning av dessa.
US5756751A (en)	1998-05-26	Compounds containing alkoxysilane groups and hydantoin groups
JP4016090B2 (ja)	2007-12-05	ヒドロキシ官能性アルコキシシランおよび該アルコキシシランから製造されたアルコキシシラン官能性ポリウレタン
CA2620991C (en)	2014-05-27	Prepolymers comprising low-viscosity alkoxysilane groups, method for the preparation and use thereof
US4345053A (en)	1982-08-17	Silicon-terminated polyurethane polymer
KR101350769B1 (ko)	2014-02-17	유기 비스무스 촉매를 사용한 아미노-실란 말단 폴리머의제조 및 비-주석 촉매를 사용하여 그로부터 경화된 폴리머
CA1163039A (en)	1984-02-28	Polyurethane sealant system
US5047546A (en)	1991-09-10	Oxazolidines containing silane groups
US6133395A (en)	2000-10-17	Polyurethane compositions
KR102628565B1 (ko)	2024-01-25	실란화된 아크릴 폴리올계 코팅에 프라이머 없이 접합하는 이소시아네이트 작용성 접착제
CA2040215A1 (en)	1991-11-30	Fast-cure polyurethane sealant composition containing silyl-subtituted guanidine accelerators
US6262296B1 (en)	2001-07-17	Polyisocyanate prepolymer
KR20060096497A (ko)	2006-09-11	Ｎｃｏ 및 실릴 반응성이 있는 폴리우레탄 조성물
CN107446111B (zh)	2020-06-02	一种含氨基甲酸酯基的硅烷封端树脂及其制备方法
US3715338A (en)	1973-02-06	Sealing compositions from polyketimines on polyenamines
US4426506A (en)	1984-01-17	Alpha-beta unsaturated ureide polymers, method for making same and cured elastomers produced therefrom
CA2107594A1 (en)	1994-04-07	Adhesion promoters
KR100500620B1 (ko)	2006-01-27	알콕시실란기및히단토인기함유화합물
WO2021069605A1 (en)	2021-04-15	One-part polyurethane sealant for low temperature applications
JPH03247617A (ja)	1991-11-05	湿気硬化性ポリウレタン組成物
CA2015040A1 (en)	1990-10-24	Two-component compositions and coatings and sealants produced therefrom
JPS63254120A (ja)	1988-10-20	水分硬化性ケイ素末端重合体
JPH03172313A (ja)	1991-07-25	湿気硬化型組成物