DD208364A5 - Nichtkristalline polyamin/kohlensaeuresalz-kompositionen - Google Patents

Nichtkristalline polyamin/kohlensaeuresalz-kompositionen Download PDF

Info

Publication number: DD208364A5
Authority: DD; German Democratic Republic
Prior art keywords: mol; water; cycloaliphatic; aliphatic; polyamines
Prior art date: 1981-10-31

Application number

DD82244391A

Other languages

German (de)

English (en)

Inventor

Werner Rasshofer

Wilhelm Thoma

Anton Schmitz

Original Assignee

Bayer 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.)

1981-10-31

Filing date

1982-10-29

Publication date

1984-05-02

1982-10-29 Application filed by Bayer Ag filed Critical Bayer Ag

1984-05-02 Publication of DD208364A5 publication Critical patent/DD208364A5/de

Links

239000000203 mixture Substances 0.000 title claims abstract description 99
229920000768 polyamine Polymers 0.000 title claims abstract description 34
-1 CARBON SALT SALT Chemical class 0.000 title description 24
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 72
125000001931 aliphatic group Chemical group 0.000 claims abstract description 22
125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 17
125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims abstract description 16
239000000654 additive Substances 0.000 claims abstract description 15
239000007788 liquid Substances 0.000 claims abstract description 15
AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 claims abstract description 13
125000003277 amino group Chemical group 0.000 claims abstract description 10
238000002360 preparation method Methods 0.000 claims abstract description 9
150000004985 diamines Chemical class 0.000 claims description 26
GQWWGRUJOCIUKI-UHFFFAOYSA-N 2-[3-(2-methyl-1-oxopyrrolo[1,2-a]pyrazin-3-yl)propyl]guanidine Chemical compound O=C1N(C)C(CCCN=C(N)N)=CN2C=CC=C21 GQWWGRUJOCIUKI-UHFFFAOYSA-N 0.000 claims description 18
239000004814 polyurethane Substances 0.000 claims description 18
229920002635 polyurethane Polymers 0.000 claims description 16
239000002904 solvent Substances 0.000 claims description 13
238000000034 method Methods 0.000 claims description 12
125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 claims description 12
230000009969 flowable effect Effects 0.000 claims description 9
239000003085 diluting agent Substances 0.000 claims description 8
150000003839 salts Chemical class 0.000 claims description 7
239000003960 organic solvent Substances 0.000 claims description 6
238000009835 boiling Methods 0.000 claims description 5
230000008569 process Effects 0.000 claims description 4
229920005575 poly(amic acid) Polymers 0.000 claims description 3
101000588924 Anthopleura elegantissima Delta-actitoxin-Ael1a Proteins 0.000 claims description 2
150000002500 ions Chemical class 0.000 claims description 2
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims 1
229910052700 potassium Inorganic materials 0.000 claims 1
239000011591 potassium Substances 0.000 claims 1
CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 abstract description 100
239000001569 carbon dioxide Substances 0.000 abstract description 50
229910002092 carbon dioxide Inorganic materials 0.000 abstract description 50
238000000576 coating method Methods 0.000 abstract description 21
239000004971 Cross linker Substances 0.000 abstract description 19
239000011248 coating agent Substances 0.000 abstract description 18
238000004519 manufacturing process Methods 0.000 abstract description 15
239000000758 substrate Substances 0.000 abstract description 12
125000005588 carbonic acid salt group Chemical group 0.000 abstract description 8
239000004970 Chain extender Substances 0.000 abstract description 7
229920003226 polyurethane urea Polymers 0.000 abstract description 6
239000003380 propellant Substances 0.000 abstract description 3
230000000996 additive effect Effects 0.000 abstract 1
239000012948 isocyanate Substances 0.000 abstract 1
150000002513 isocyanates Chemical class 0.000 abstract 1
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 39
239000006260 foam Substances 0.000 description 29
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 26
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 25
150000001875 compounds Chemical class 0.000 description 23
239000000853 adhesive Substances 0.000 description 22
230000001070 adhesive effect Effects 0.000 description 22
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 20
238000006243 chemical reaction Methods 0.000 description 19
239000000047 product Substances 0.000 description 19
239000000243 solution Substances 0.000 description 19
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 17
PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 16
VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 12
150000001412 amines Chemical class 0.000 description 11
238000001816 cooling Methods 0.000 description 11
239000007789 gas Substances 0.000 description 10
IGSBHTZEJMPDSZ-UHFFFAOYSA-N 4-[(4-amino-3-methylcyclohexyl)methyl]-2-methylcyclohexan-1-amine Chemical compound C1CC(N)C(C)CC1CC1CC(C)C(N)CC1 IGSBHTZEJMPDSZ-UHFFFAOYSA-N 0.000 description 9
150000004649 carbonic acid derivatives Chemical class 0.000 description 9
229910052757 nitrogen Inorganic materials 0.000 description 9
239000000049 pigment Substances 0.000 description 9
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 8
WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 8
238000004132 cross linking Methods 0.000 description 8
238000000354 decomposition reaction Methods 0.000 description 8
239000002244 precipitate Substances 0.000 description 8
238000003860 storage Methods 0.000 description 8
RNLHGQLZWXBQNY-UHFFFAOYSA-N 3-(aminomethyl)-3,5,5-trimethylcyclohexan-1-amine Chemical compound CC1(C)CC(N)CC(C)(CN)C1 RNLHGQLZWXBQNY-UHFFFAOYSA-N 0.000 description 7
BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 7
239000002253 acid Substances 0.000 description 7
229920000728 polyester Polymers 0.000 description 7
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
239000004604 Blowing Agent Substances 0.000 description 6
BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 6
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 6
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 6
238000002844 melting Methods 0.000 description 6
239000005056 polyisocyanate Substances 0.000 description 6
229920001228 polyisocyanate Polymers 0.000 description 6
229920005862 polyol Polymers 0.000 description 6
229920001296 polysiloxane Polymers 0.000 description 6
QOXOZONBQWIKDA-UHFFFAOYSA-N 3-hydroxypropyl Chemical group [CH2]CCO QOXOZONBQWIKDA-UHFFFAOYSA-N 0.000 description 5
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
229920002396 Polyurea Polymers 0.000 description 5
125000003118 aryl group Chemical group 0.000 description 5
239000008199 coating composition Substances 0.000 description 5
239000004744 fabric Substances 0.000 description 5
NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 5
239000010985 leather Substances 0.000 description 5
230000008018 melting Effects 0.000 description 5
239000002798 polar solvent Substances 0.000 description 5
150000003077 polyols Chemical class 0.000 description 5
239000011541 reaction mixture Substances 0.000 description 5
239000007787 solid Substances 0.000 description 5
239000000126 substance Substances 0.000 description 5
239000004753 textile Substances 0.000 description 5
230000009974 thixotropic effect Effects 0.000 description 5
ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 4
UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 4
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 4
239000001361 adipic acid Substances 0.000 description 4
235000011037 adipic acid Nutrition 0.000 description 4
LHIJANUOQQMGNT-UHFFFAOYSA-N aminoethylethanolamine Chemical compound NCCNCCO LHIJANUOQQMGNT-UHFFFAOYSA-N 0.000 description 4
WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 4
239000003054 catalyst Substances 0.000 description 4
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 4
125000005442 diisocyanate group Chemical group 0.000 description 4
239000000463 material Substances 0.000 description 4
238000002156 mixing Methods 0.000 description 4
230000000630 rising effect Effects 0.000 description 4
239000003381 stabilizer Substances 0.000 description 4
239000000454 talc Substances 0.000 description 4
235000012222 talc Nutrition 0.000 description 4
229910052623 talc Inorganic materials 0.000 description 4
RSJKGSCJYJTIGS-UHFFFAOYSA-N undecane Chemical compound CCCCCCCCCCC RSJKGSCJYJTIGS-UHFFFAOYSA-N 0.000 description 4
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 3
DZIHTWJGPDVSGE-UHFFFAOYSA-N 4-[(4-aminocyclohexyl)methyl]cyclohexan-1-amine Chemical compound C1CC(N)CCC1CC1CCC(N)CC1 DZIHTWJGPDVSGE-UHFFFAOYSA-N 0.000 description 3
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 description 3
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 3
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
239000002981 blocking agent Substances 0.000 description 3
150000005323 carbonate salts Chemical class 0.000 description 3
BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 3
238000001035 drying Methods 0.000 description 3
125000002768 hydroxyalkyl group Chemical group 0.000 description 3
239000000155 melt Substances 0.000 description 3
125000001302 tertiary amino group Chemical group 0.000 description 3
HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
XLLIQLLCWZCATF-UHFFFAOYSA-N 2-methoxyethyl acetate Chemical compound COCCOC(C)=O XLLIQLLCWZCATF-UHFFFAOYSA-N 0.000 description 2
WADSJYLPJPTMLN-UHFFFAOYSA-N 3-(cycloundecen-1-yl)-1,2-diazacycloundec-2-ene Chemical compound C1CCCCCCCCC=C1C1=NNCCCCCCCC1 WADSJYLPJPTMLN-UHFFFAOYSA-N 0.000 description 2
KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 2
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical class OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 2
XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 2
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
239000005058 Isophorone diisocyanate Substances 0.000 description 2
FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 2
BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 2
GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 2
NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 2
ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 2
UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
OTBHHUPVCYLGQO-UHFFFAOYSA-N bis(3-aminopropyl)amine Chemical compound NCCCNCCCN OTBHHUPVCYLGQO-UHFFFAOYSA-N 0.000 description 2
238000007664 blowing Methods 0.000 description 2
VHRGRCVQAFMJIZ-UHFFFAOYSA-N cadaverine Chemical compound NCCCCCN VHRGRCVQAFMJIZ-UHFFFAOYSA-N 0.000 description 2
150000004657 carbamic acid derivatives Chemical class 0.000 description 2
125000004432 carbon atom Chemical group C* 0.000 description 2
KXDHJXZQYSOELW-UHFFFAOYSA-N carbonic acid monoamide Natural products NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 description 2
239000007795 chemical reaction product Substances 0.000 description 2
239000003795 chemical substances by application Substances 0.000 description 2
PAFZNILMFXTMIY-UHFFFAOYSA-N cyclohexylamine Chemical compound NC1CCCCC1 PAFZNILMFXTMIY-UHFFFAOYSA-N 0.000 description 2
239000012975 dibutyltin dilaurate Substances 0.000 description 2
239000004205 dimethyl polysiloxane Substances 0.000 description 2
235000013870 dimethyl polysiloxane Nutrition 0.000 description 2
150000002148 esters Chemical class 0.000 description 2
150000002170 ethers Chemical class 0.000 description 2
239000000945 filler Substances 0.000 description 2
238000005187 foaming Methods 0.000 description 2
238000010438 heat treatment Methods 0.000 description 2
ACCCMOQWYVYDOT-UHFFFAOYSA-N hexane-1,1-diol Chemical compound CCCCCC(O)O ACCCMOQWYVYDOT-UHFFFAOYSA-N 0.000 description 2
230000000977 initiatory effect Effects 0.000 description 2
PHTQWCKDNZKARW-UHFFFAOYSA-N isoamylol Chemical compound CC(C)CCO PHTQWCKDNZKARW-UHFFFAOYSA-N 0.000 description 2
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 2
150000002576 ketones Chemical class 0.000 description 2
238000010030 laminating Methods 0.000 description 2
238000003475 lamination Methods 0.000 description 2
BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
239000012452 mother liquor Substances 0.000 description 2
SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 2
239000004745 nonwoven fabric Substances 0.000 description 2
FDPIMTJIUBPUKL-UHFFFAOYSA-N pentan-3-one Chemical compound CCC(=O)CC FDPIMTJIUBPUKL-UHFFFAOYSA-N 0.000 description 2
238000005191 phase separation Methods 0.000 description 2
229920000435 poly(dimethylsiloxane) Polymers 0.000 description 2
239000004417 polycarbonate Substances 0.000 description 2
229920000515 polycarbonate Polymers 0.000 description 2
229920001451 polypropylene glycol Polymers 0.000 description 2
BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
239000001294 propane Substances 0.000 description 2
WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical compound CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 description 2
AOHJOMMDDJHIJH-UHFFFAOYSA-N propylenediamine Chemical compound CC(N)CN AOHJOMMDDJHIJH-UHFFFAOYSA-N 0.000 description 2
KIDHWZJUCRJVML-UHFFFAOYSA-N putrescine Chemical compound NCCCCN KIDHWZJUCRJVML-UHFFFAOYSA-N 0.000 description 2
230000009257 reactivity Effects 0.000 description 2
239000011833 salt mixture Substances 0.000 description 2
239000007858 starting material Substances 0.000 description 2
LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 2
NDFDKKKMPXHSJA-UHFFFAOYSA-N undecane-1,5,11-triamine Chemical compound NCCCCCCC(N)CCCCN NDFDKKKMPXHSJA-UHFFFAOYSA-N 0.000 description 2
XSQUKJJJFZCRTK-UHFFFAOYSA-N urea group Chemical group NC(=O)N XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
NWZSZGALRFJKBT-KNIFDHDWSA-N (2s)-2,6-diaminohexanoic acid;(2s)-2-hydroxybutanedioic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O.NCCCC[C@H](N)C(O)=O NWZSZGALRFJKBT-KNIFDHDWSA-N 0.000 description 1
ZWVMLYRJXORSEP-LURJTMIESA-N (2s)-hexane-1,2,6-triol Chemical compound OCCCC[C@H](O)CO ZWVMLYRJXORSEP-LURJTMIESA-N 0.000 description 1
WHIVNJATOVLWBW-PLNGDYQASA-N (nz)-n-butan-2-ylidenehydroxylamine Chemical compound CC\C(C)=N/O WHIVNJATOVLWBW-PLNGDYQASA-N 0.000 description 1
QGLWBTPVKHMVHM-KTKRTIGZSA-N (z)-octadec-9-en-1-amine Chemical compound CCCCCCCC\C=C/CCCCCCCCN QGLWBTPVKHMVHM-KTKRTIGZSA-N 0.000 description 1
AVQQQNCBBIEMEU-UHFFFAOYSA-N 1,1,3,3-tetramethylurea Chemical compound CN(C)C(=O)N(C)C AVQQQNCBBIEMEU-UHFFFAOYSA-N 0.000 description 1
BOJZPUPAXYETRK-UHFFFAOYSA-N 1,1-diphenylethane-1,2-diamine Chemical compound C=1C=CC=CC=1C(N)(CN)C1=CC=CC=C1 BOJZPUPAXYETRK-UHFFFAOYSA-N 0.000 description 1
ASCFOGLXLHNFFE-UHFFFAOYSA-N 1,4-dioxane 2-methylpropan-1-ol Chemical compound O1CCOCC1.C(C(C)C)O ASCFOGLXLHNFFE-UHFFFAOYSA-N 0.000 description 1
CWKVFRNCODQPDB-UHFFFAOYSA-N 1-(2-aminoethylamino)propan-2-ol Chemical compound CC(O)CNCCN CWKVFRNCODQPDB-UHFFFAOYSA-N 0.000 description 1
AWNXKZVIZARMME-UHFFFAOYSA-N 1-[[5-[2-[(2-chloropyridin-4-yl)amino]pyrimidin-4-yl]-4-(cyclopropylmethyl)pyrimidin-2-yl]amino]-2-methylpropan-2-ol Chemical compound N=1C(NCC(C)(O)C)=NC=C(C=2N=C(NC=3C=C(Cl)N=CC=3)N=CC=2)C=1CC1CC1 AWNXKZVIZARMME-UHFFFAOYSA-N 0.000 description 1
QFPSWHHWTPBRCL-UHFFFAOYSA-N 1-[ethyl(2-hydroxypropyl)amino]propan-2-ol Chemical compound CC(O)CN(CC)CC(C)O QFPSWHHWTPBRCL-UHFFFAOYSA-N 0.000 description 1
CFGWPTDWIBCXMS-UHFFFAOYSA-N 1-[hexyl(2-hydroxypropyl)amino]propan-2-ol Chemical compound CCCCCCN(CC(C)O)CC(C)O CFGWPTDWIBCXMS-UHFFFAOYSA-N 0.000 description 1
HXKKHQJGJAFBHI-UHFFFAOYSA-N 1-aminopropan-2-ol Chemical class CC(O)CN HXKKHQJGJAFBHI-UHFFFAOYSA-N 0.000 description 1
PCQPOHNESISPQI-UHFFFAOYSA-N 1-methyl-4-propan-2-ylcyclohexane-1,3-diamine Chemical compound CC(C)C1CCC(C)(N)CC1N PCQPOHNESISPQI-UHFFFAOYSA-N 0.000 description 1
JCUZDQXWVYNXHD-UHFFFAOYSA-N 2,2,4-trimethylhexane-1,6-diamine Chemical compound NCCC(C)CC(C)(C)CN JCUZDQXWVYNXHD-UHFFFAOYSA-N 0.000 description 1
NSMWYRLQHIXVAP-UHFFFAOYSA-N 2,5-dimethylpiperazine Chemical compound CC1CNC(C)CN1 NSMWYRLQHIXVAP-UHFFFAOYSA-N 0.000 description 1
AJTNPTIVLIQFSR-UHFFFAOYSA-N 2-[2-[bis(2-hydroxyethyl)amino]ethylamino]ethanol Chemical compound OCCNCCN(CCO)CCO AJTNPTIVLIQFSR-UHFFFAOYSA-N 0.000 description 1
GVNHOISKXMSMPX-UHFFFAOYSA-N 2-[butyl(2-hydroxyethyl)amino]ethanol Chemical compound CCCCN(CCO)CCO GVNHOISKXMSMPX-UHFFFAOYSA-N 0.000 description 1
UXFQFBNBSPQBJW-UHFFFAOYSA-N 2-amino-2-methylpropane-1,3-diol Chemical compound OCC(N)(C)CO UXFQFBNBSPQBJW-UHFFFAOYSA-N 0.000 description 1
JCBPETKZIGVZRE-UHFFFAOYSA-N 2-aminobutan-1-ol Chemical compound CCC(N)CO JCBPETKZIGVZRE-UHFFFAOYSA-N 0.000 description 1
BKMMTJMQCTUHRP-UHFFFAOYSA-N 2-aminopropan-1-ol Chemical compound CC(N)CO BKMMTJMQCTUHRP-UHFFFAOYSA-N 0.000 description 1
ANKIUPGAZUYELN-UHFFFAOYSA-N 2-hexoxyethyl acetate Chemical compound CCCCCCOCCOC(C)=O ANKIUPGAZUYELN-UHFFFAOYSA-N 0.000 description 1
ZAXCZCOUDLENMH-UHFFFAOYSA-N 3,3,3-tetramine Chemical compound NCCCNCCCNCCCN ZAXCZCOUDLENMH-UHFFFAOYSA-N 0.000 description 1
WTAAMFMRJQMJCK-UHFFFAOYSA-N 3-(1-aminoethyl)-3,5,5-trimethylcyclohexan-1-amine Chemical compound CC(N)C1(C)CC(N)CC(C)(C)C1 WTAAMFMRJQMJCK-UHFFFAOYSA-N 0.000 description 1
CXMYWOCYTPKBPP-UHFFFAOYSA-N 3-(3-hydroxypropylamino)propan-1-ol Chemical compound OCCCNCCCO CXMYWOCYTPKBPP-UHFFFAOYSA-N 0.000 description 1
YFEAYNIMJBHJCM-UHFFFAOYSA-N 3-(aminomethyl)-3,5,5-trimethylcyclohexan-1-ol Chemical compound CC1(C)CC(O)CC(C)(CN)C1 YFEAYNIMJBHJCM-UHFFFAOYSA-N 0.000 description 1
NEXHFUYVHMVDTG-UHFFFAOYSA-N 3-[2-[bis(3-hydroxypropyl)amino]ethylamino]propan-1-ol Chemical compound OCCCNCCN(CCCO)CCCO NEXHFUYVHMVDTG-UHFFFAOYSA-N 0.000 description 1
WMRXHQRDCIXTCD-UHFFFAOYSA-N 3-hydrazinylpropan-1-ol Chemical compound NNCCCO WMRXHQRDCIXTCD-UHFFFAOYSA-N 0.000 description 1
125000006291 3-hydroxybenzyl group Chemical group [H]OC1=C([H])C([H])=C([H])C(=C1[H])C([H])([H])* 0.000 description 1
OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
FDPCVOXXUBYMTQ-UHFFFAOYSA-N 4-(4-aminobutoxy)butan-1-amine Chemical compound NCCCCOCCCCN FDPCVOXXUBYMTQ-UHFFFAOYSA-N 0.000 description 1
OZUBMBIDHPBIDL-UHFFFAOYSA-N 4-Propylcyclohexylamine Chemical compound CCCC1CCC(N)CC1 OZUBMBIDHPBIDL-UHFFFAOYSA-N 0.000 description 1
OCQPCWPMJRXPCD-UHFFFAOYSA-N 4-[1-(4-amino-3-methylcyclohexyl)cyclohexyl]-2-methylcyclohexan-1-amine Chemical compound C1CC(N)C(C)CC1C1(C2CC(C)C(N)CC2)CCCCC1 OCQPCWPMJRXPCD-UHFFFAOYSA-N 0.000 description 1
GDLGGBXEOMDKCV-UHFFFAOYSA-N 4-[1-(4-aminocyclohexyl)cyclohexyl]cyclohexan-1-amine Chemical compound C1CC(N)CCC1C1(C2CCC(N)CC2)CCCCC1 GDLGGBXEOMDKCV-UHFFFAOYSA-N 0.000 description 1
BDBZTOMUANOKRT-UHFFFAOYSA-N 4-[2-(4-aminocyclohexyl)propan-2-yl]cyclohexan-1-amine Chemical compound C1CC(N)CCC1C(C)(C)C1CCC(N)CC1 BDBZTOMUANOKRT-UHFFFAOYSA-N 0.000 description 1
QTKDDPSHNLZGRO-UHFFFAOYSA-N 4-methylcyclohexane-1,3-diamine Chemical compound CC1CCC(N)CC1N QTKDDPSHNLZGRO-UHFFFAOYSA-N 0.000 description 1
RGFWQLHALIZEQV-UHFFFAOYSA-N 5-amino-3-methylpentan-1-ol Chemical compound NCCC(C)CCO RGFWQLHALIZEQV-UHFFFAOYSA-N 0.000 description 1
SUTWPJHCRAITLU-UHFFFAOYSA-N 6-aminohexan-1-ol Chemical compound NCCCCCCO SUTWPJHCRAITLU-UHFFFAOYSA-N 0.000 description 1
229920000742 Cotton Polymers 0.000 description 1
RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 1
JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Natural products OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 description 1
239000004831 Hot glue Substances 0.000 description 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
RJUFJBKOKNCXHH-UHFFFAOYSA-N Methyl propionate Chemical compound CCC(=O)OC RJUFJBKOKNCXHH-UHFFFAOYSA-N 0.000 description 1
229920001730 Moisture cure polyurethane Polymers 0.000 description 1
241001502129 Mullus Species 0.000 description 1
CJKRXEBLWJVYJD-UHFFFAOYSA-N N,N'-diethylethylenediamine Chemical compound CCNCCNCC CJKRXEBLWJVYJD-UHFFFAOYSA-N 0.000 description 1
SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
239000004952 Polyamide Substances 0.000 description 1
239000004698 Polyethylene Substances 0.000 description 1
239000004721 Polyphenylene oxide Substances 0.000 description 1
229920005830 Polyurethane Foam Polymers 0.000 description 1
XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
239000005700 Putrescine Substances 0.000 description 1
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical class [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
229910000831 Steel Inorganic materials 0.000 description 1
AWMVMTVKBNGEAK-UHFFFAOYSA-N Styrene oxide Chemical compound C1OC1C1=CC=CC=C1 AWMVMTVKBNGEAK-UHFFFAOYSA-N 0.000 description 1
239000007983 Tris buffer Substances 0.000 description 1
FHKPLLOSJHHKNU-INIZCTEOSA-N [(3S)-3-[8-(1-ethyl-5-methylpyrazol-4-yl)-9-methylpurin-6-yl]oxypyrrolidin-1-yl]-(oxan-4-yl)methanone Chemical compound C(C)N1N=CC(=C1C)C=1N(C2=NC=NC(=C2N=1)O[C@@H]1CN(CC1)C(=O)C1CCOCC1)C FHKPLLOSJHHKNU-INIZCTEOSA-N 0.000 description 1
LNWBFIVSTXCJJG-UHFFFAOYSA-N [diisocyanato(phenyl)methyl]benzene Chemical compound C=1C=CC=CC=1C(N=C=O)(N=C=O)C1=CC=CC=C1 LNWBFIVSTXCJJG-UHFFFAOYSA-N 0.000 description 1
230000009471 action Effects 0.000 description 1
230000001476 alcoholic effect Effects 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
125000000217 alkyl group Chemical group 0.000 description 1
125000002947 alkylene group Chemical group 0.000 description 1
125000005263 alkylenediamine group Chemical group 0.000 description 1
150000001408 amides Chemical class 0.000 description 1
CBTVGIZVANVGBH-UHFFFAOYSA-N aminomethyl propanol Chemical compound CC(C)(N)CO CBTVGIZVANVGBH-UHFFFAOYSA-N 0.000 description 1
239000012223 aqueous fraction Substances 0.000 description 1
230000008901 benefit Effects 0.000 description 1
150000001565 benzotriazoles Chemical class 0.000 description 1
RNSLCHIAOHUARI-UHFFFAOYSA-N butane-1,4-diol;hexanedioic acid Chemical compound OCCCCO.OC(=O)CCCCC(O)=O RNSLCHIAOHUARI-UHFFFAOYSA-N 0.000 description 1
239000004202 carbamide Substances 0.000 description 1
235000013877 carbamide Nutrition 0.000 description 1
150000001720 carbohydrates Chemical class 0.000 description 1
235000014633 carbohydrates Nutrition 0.000 description 1
ZNRRUPOIAJUGKV-UHFFFAOYSA-N carbon dioxide;chlorobenzene Chemical compound O=C=O.ClC1=CC=CC=C1 ZNRRUPOIAJUGKV-UHFFFAOYSA-N 0.000 description 1
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical class OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 1
230000000052 comparative effect Effects 0.000 description 1
239000002131 composite material Substances 0.000 description 1
238000009833 condensation Methods 0.000 description 1
230000005494 condensation Effects 0.000 description 1
238000010276 construction Methods 0.000 description 1
239000012084 conversion product Substances 0.000 description 1
239000003431 cross linking reagent Substances 0.000 description 1
UYAUGHKQCCCFDK-UHFFFAOYSA-N cyclohexane-1,3,5-triamine Chemical compound NC1CC(N)CC(N)C1 UYAUGHKQCCCFDK-UHFFFAOYSA-N 0.000 description 1
XXKOQQBKBHUATC-UHFFFAOYSA-N cyclohexylmethylcyclohexane Chemical compound C1CCCCC1CC1CCCCC1 XXKOQQBKBHUATC-UHFFFAOYSA-N 0.000 description 1
NISGSNTVMOOSJQ-UHFFFAOYSA-N cyclopentanamine Chemical compound NC1CCCC1 NISGSNTVMOOSJQ-UHFFFAOYSA-N 0.000 description 1
YQLZOAVZWJBZSY-UHFFFAOYSA-N decane-1,10-diamine Chemical compound NCCCCCCCCCCN YQLZOAVZWJBZSY-UHFFFAOYSA-N 0.000 description 1
230000003111 delayed effect Effects 0.000 description 1
238000001514 detection method Methods 0.000 description 1
VZRUGPJUVWRHKM-UHFFFAOYSA-N dibutylhexamethylenediamine Chemical compound CCCCNCCCCCCNCCCC VZRUGPJUVWRHKM-UHFFFAOYSA-N 0.000 description 1
KORSJDCBLAPZEQ-UHFFFAOYSA-N dicyclohexylmethane-4,4'-diisocyanate Chemical compound C1CC(N=C=O)CCC1CC1CCC(N=C=O)CC1 KORSJDCBLAPZEQ-UHFFFAOYSA-N 0.000 description 1
ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
238000010790 dilution Methods 0.000 description 1
239000012895 dilution Substances 0.000 description 1
150000002009 diols Chemical class 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
QFTYSVGGYOXFRQ-UHFFFAOYSA-N dodecane-1,12-diamine Chemical compound NCCCCCCCCCCCCN QFTYSVGGYOXFRQ-UHFFFAOYSA-N 0.000 description 1
238000009820 dry lamination Methods 0.000 description 1
239000000975 dye Substances 0.000 description 1
239000003995 emulsifying agent Substances 0.000 description 1
150000002168 ethanoic acid esters Chemical class 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
230000002349 favourable effect Effects 0.000 description 1
239000003063 flame retardant Substances 0.000 description 1
235000019253 formic acid Nutrition 0.000 description 1
WBJINCZRORDGAQ-UHFFFAOYSA-N formic acid ethyl ester Natural products CCOC=O WBJINCZRORDGAQ-UHFFFAOYSA-N 0.000 description 1
238000009472 formulation Methods 0.000 description 1
229910021485 fumed silica Inorganic materials 0.000 description 1
238000003958 fumigation Methods 0.000 description 1
230000030279 gene silencing Effects 0.000 description 1
210000004907 gland Anatomy 0.000 description 1
125000005842 heteroatom Chemical group 0.000 description 1
IKDUDTNKRLTJSI-UHFFFAOYSA-N hydrazine monohydrate Substances O.NN IKDUDTNKRLTJSI-UHFFFAOYSA-N 0.000 description 1
150000002429 hydrazines Chemical class 0.000 description 1
239000001257 hydrogen Substances 0.000 description 1
229910052739 hydrogen Inorganic materials 0.000 description 1
150000004680 hydrogen peroxides Chemical class 0.000 description 1
239000011261 inert gas Substances 0.000 description 1
238000011835 investigation Methods 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
IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 1
JJWLVOIRVHMVIS-UHFFFAOYSA-N isopropylamine Chemical compound CC(C)N JJWLVOIRVHMVIS-UHFFFAOYSA-N 0.000 description 1
150000003951 lactams Chemical class 0.000 description 1
239000002649 leather substitute Substances 0.000 description 1
239000011159 matrix material Substances 0.000 description 1
MDEDOIDXVJXDBW-UHFFFAOYSA-N methoxymethyl acetate Chemical compound COCOC(C)=O MDEDOIDXVJXDBW-UHFFFAOYSA-N 0.000 description 1
229940017219 methyl propionate Drugs 0.000 description 1
239000003607 modifier Substances 0.000 description 1
KMBPCQSCMCEPMU-UHFFFAOYSA-N n'-(3-aminopropyl)-n'-methylpropane-1,3-diamine Chemical compound NCCCN(C)CCCN KMBPCQSCMCEPMU-UHFFFAOYSA-N 0.000 description 1
KFIGICHILYTCJF-UHFFFAOYSA-N n'-methylethane-1,2-diamine Chemical compound CNCCN KFIGICHILYTCJF-UHFFFAOYSA-N 0.000 description 1
WHQSYGRFZMUQGQ-UHFFFAOYSA-N n,n-dimethylformamide;hydrate Chemical compound O.CN(C)C=O WHQSYGRFZMUQGQ-UHFFFAOYSA-N 0.000 description 1
230000006855 networking Effects 0.000 description 1
GAZIERBSBYYJJW-UHFFFAOYSA-N octane-1,3-diamine Chemical compound CCCCCC(N)CCN GAZIERBSBYYJJW-UHFFFAOYSA-N 0.000 description 1
150000002923 oximes Chemical class 0.000 description 1
239000002245 particle Substances 0.000 description 1
235000011837 pasties Nutrition 0.000 description 1
230000035515 penetration Effects 0.000 description 1
WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
239000000575 pesticide Substances 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
PVCOXMQIAVGPJN-UHFFFAOYSA-N piperazine-1,4-diamine Chemical compound NN1CCN(N)CC1 PVCOXMQIAVGPJN-UHFFFAOYSA-N 0.000 description 1
229920003023 plastic Polymers 0.000 description 1
239000004033 plastic Substances 0.000 description 1
239000004014 plasticizer Substances 0.000 description 1
229920000058 polyacrylate Polymers 0.000 description 1
229920002647 polyamide Polymers 0.000 description 1
229920000570 polyether Polymers 0.000 description 1
229920000573 polyethylene Polymers 0.000 description 1
239000011496 polyurethane foam Substances 0.000 description 1
239000011148 porous material Substances 0.000 description 1
230000001376 precipitating effect Effects 0.000 description 1
238000001556 precipitation Methods 0.000 description 1
150000003141 primary amines Chemical class 0.000 description 1
230000037452 priming Effects 0.000 description 1
238000007639 printing Methods 0.000 description 1
238000012545 processing Methods 0.000 description 1
239000000376 reactant Substances 0.000 description 1
238000011084 recovery Methods 0.000 description 1
238000010992 reflux Methods 0.000 description 1
238000002407 reforming Methods 0.000 description 1
230000003014 reinforcing effect Effects 0.000 description 1
238000007650 screen-printing Methods 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
229920002545 silicone oil Polymers 0.000 description 1
238000005245 sintering Methods 0.000 description 1
238000007767 slide coating Methods 0.000 description 1
239000011877 solvent mixture Substances 0.000 description 1
239000010959 steel Substances 0.000 description 1
238000003756 stirring Methods 0.000 description 1
238000000859 sublimation Methods 0.000 description 1
230000008022 sublimation Effects 0.000 description 1
150000005846 sugar alcohols Polymers 0.000 description 1
HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 description 1
125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 1
239000013589 supplement Substances 0.000 description 1
239000000725 suspension Substances 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
150000003509 tertiary alcohols Chemical class 0.000 description 1
FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 description 1
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
229920001187 thermosetting polymer Polymers 0.000 description 1
230000008719 thickening Effects 0.000 description 1
KJAMZCVTJDTESW-UHFFFAOYSA-N tiracizine Chemical class C1CC2=CC=CC=C2N(C(=O)CN(C)C)C2=CC(NC(=O)OCC)=CC=C21 KJAMZCVTJDTESW-UHFFFAOYSA-N 0.000 description 1
DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 1
238000012549 training Methods 0.000 description 1
238000012546 transfer Methods 0.000 description 1
150000003673 urethanes Chemical class 0.000 description 1
238000005406 washing Methods 0.000 description 1
239000002759 woven fabric Substances 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

Landscapes

Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Polyurethanes Or Polyureas (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Paints Or Removers (AREA)
Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)

DD82244391A 1981-10-31 1982-10-29 Nichtkristalline polyamin/kohlensaeuresalz-kompositionen DD208364A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19813143253 DE3143253A1 (de)	1981-10-31	1981-10-31	Nichtkristalline polyamin/kohlensaeuresalz-kompositionen, ein verfahren zu ihrer herstellung und ihre verwendung zur herstellung von polyurethanharnstoffen, speziell geschaeumten beschichtungen

Publications (1)

Publication Number	Publication Date
DD208364A5 true DD208364A5 (de)	1984-05-02

Family

ID=6145293

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD82244391A DD208364A5 (de)	1981-10-31	1982-10-29	Nichtkristalline polyamin/kohlensaeuresalz-kompositionen

Country Status (7)

Country	Link
US (1)	US4469856A (cs)
EP (1)	EP0078436B1 (cs)
JP (1)	JPS58113150A (cs)
CA (1)	CA1199147A (cs)
CS (1)	CS233738B2 (cs)
DD (1)	DD208364A5 (cs)
DE (2)	DE3143253A1 (cs)

Families Citing this family (18)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE3312215A1 (de) *	1983-04-05	1984-10-11	Bayer Ag, 5090 Leverkusen	Verfahren zur herstellung eines zelligen polyurethans
US4980388A (en) *	1988-10-17	1990-12-25	The Dow Chemical Company	Use of carbon dioxide adducts as blowing agents in cellular and microcellular polyureas
US5209969A (en) *	1992-02-07	1993-05-11	W. L. Gore & Associates, Inc.	Carbamate/urethane composition and textile lamination process
US5789451A (en) *	1996-07-29	1998-08-04	The Dow Chemcial Company	Alkanolamine/carbon dioxide adduct and polyurethane foam therewith
US5726251A (en) *	1996-10-11	1998-03-10	Air Products And Chemicals, Inc.	Powder coatings of amine-reactive resins and amine carbamate salts
AU2005245950A1 (en) *	2004-05-19	2005-12-01	Flexcon Company, Inc.	Liquid formulations for coating and printing substrates
US20090076222A1 (en) *	2007-09-14	2009-03-19	Pugne David R	Clear functional coating for elastomers
US20120041088A1 (en) *	2009-04-24	2012-02-16	Masaki Ishida	Foaming additive for producing polyurethane foam, and method for producing rigid polyurethane foam by using it
JP2011026391A (ja) *	2009-07-22	2011-02-10	Tosoh Corp	スプレー式硬質ポリウレタンフォームの製造方法
JP2011037951A (ja) *	2009-08-07	2011-02-24	Tosoh Corp	ポリウレタンフォーム製造用の発泡性添加剤、及びそれを用いた硬質ポリウレタンフォームの製造方法
JP2010270324A (ja) *	2009-04-24	2010-12-02	Tosoh Corp	ポリウレタンフォーム用の発泡性添加剤、及びそれを用いた硬質ポリウレタンフォームの製造方法
US20140024800A1 (en) *	2012-07-17	2014-01-23	University Of North Dakota	Carbon dioxide capture and conversion to a carbamate salt and polyurea
US10626290B2 (en) *	2013-12-16	2020-04-21	Ppg Industries Ohio, Inc.	Method of extending pot life of coating compositions
EP4585630A4 (en) *	2022-09-08	2025-12-24	Mitsubishi Gas Chemical Co	Composition of moldable expanded resin, body of polyurate-based resin foam, and process for producing a body of polyurate-based resin foam
CN116731381B (zh) *	2023-05-16	2025-01-28	四川大学	一种含二氧化碳加合物的液态发泡剂
CN116731382B (zh) *	2023-05-16	2025-07-04	四川大学	一种二氧化碳型潜发泡剂的溶剂
CN116535726B (zh) *	2023-05-18	2025-01-24	四川大学	一种可吸收二氧化碳的液态混合物用于聚氨酯泡沫
CN116874867B (zh) *	2023-07-24	2024-08-20	四川大学	一种主链含醚键的多胺聚合物的二氧化碳加合物发泡剂

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2855384A (en) *	1949-11-02	1958-10-07	Bayer Ag	Process for producing linear polyureas
DE838217C (de) *	1949-11-02	1952-05-05	Bayer Ag	Verfahren zur Herstellung von linearen Polyharnstoffen
CA764543A (en) *	1963-02-16	1967-08-01	Farbenfabriken Bayer Aktiengesellschaft	Substantially linear polyaddition polymers
FR1413484A (fr) *	1963-11-07	1965-10-08	Bayer Ag	Procédé de préparation de polyurées ou de polyamides d'acide hydrazodicarboxylique contenant des groupes hydroxyle alcooliques
US3425964A (en) *	1964-10-09	1969-02-04	Nat Starch Chem Corp	Latent curing agents for thermosetting polymers
DE1810924A1 (de) *	1968-11-26	1970-06-18	Basf Ag	Verfahren zur Trennung von Gemischen von stereoisomeren Diaminodicyclohexylalkanen
JPS5138333B2 (cs) *	1973-09-03	1976-10-21

1981
- 1981-10-31 DE DE19813143253 patent/DE3143253A1/de not_active Withdrawn
1982
- 1982-10-18 DE DE8282109596T patent/DE3262162D1/de not_active Expired
- 1982-10-18 US US06/434,788 patent/US4469856A/en not_active Expired - Fee Related
- 1982-10-18 CA CA000413642A patent/CA1199147A/en not_active Expired
- 1982-10-18 EP EP82109596A patent/EP0078436B1/de not_active Expired
- 1982-10-28 CS CS827678A patent/CS233738B2/cs unknown
- 1982-10-29 JP JP57189392A patent/JPS58113150A/ja active Pending
- 1982-10-29 DD DD82244391A patent/DD208364A5/de unknown

Also Published As

Publication number	Publication date
EP0078436A1 (de)	1983-05-11
EP0078436B1 (de)	1985-01-30
DE3143253A1 (de)	1983-05-26
CA1199147A (en)	1986-01-07
DE3262162D1 (en)	1985-03-14
JPS58113150A (ja)	1983-07-05
CS233738B2 (en)	1985-03-14
US4469856A (en)	1984-09-04

Publication	Publication Date	Title
DD208364A5 (de)	1984-05-02	Nichtkristalline polyamin/kohlensaeuresalz-kompositionen
EP0073392B1 (de)	1986-12-10	Überzugmittel aus Polyurethan-Dispersionen und ihre Verwendung für Deckstriche und Finishs
DE2141807C2 (de)	1983-09-22	Selbstemulgierter wäßriger Polyurethanharnstoff- oder Polyharnstoff-Latex und dessen Verwendung zur Herstellung von Filmen
DE2221751C3 (de)	1978-08-10	Polyurethanharnstoff elastomere
DE3116445C2 (cs)	1992-11-12
DE2446440A1 (de)	1976-04-08	Verfahren zur herstellung von polyurethanen
DE2902090A1 (de)	1980-07-24	Hitzehaertbare beschichtungsmassen und verfahren zur beschichtung von substraten
DE2912864C2 (de)	1982-03-25	Polyurethan-Bahnmaterial und Verfahren zu seiner Herstellung
DE1902932A1 (de)	1970-08-20	Semicarbazidarylamine als Kettenverlaengerungsmittel fuer Elastomerfaeden
DE2345257B1 (de)	1975-02-06	Verfahren zur Herstellung von mikroporoesen Flaechengebilden auf Polyurethanbasis
DE1170628B (de)	1964-05-21	Verfahren zur Herstellung von, gegebenenfalls verschaeumten, Polyurethanen
DE1795449A1 (de)	1972-01-05	Verfahren zur Herstellung von neuen Polyisocyanatverbindungen und von Formkoerpern
EP0154768B1 (de)	1988-05-25	Verfahren zur Herstellung von Polyurethanen, Polyurethane mit aromatischen Aminoendgruppen und ihre Verwendung
DE1770591A1 (de)	1971-11-04	Lineare,segmentierte Polyurethanelastomere
DE1237306B (de)	1967-03-23	Verfahren zur Herstellung von Polyurethankunststoffen
DE2520814A1 (de)	1976-11-18	Lichtstabilisierung von polyurethanen
DE1069379B (de)	1959-11-19	Verfahren zur Herstellung homogener Kunststoffe auf Grundlage Urethangrup'pen und gegebenenfalls auch Thioärhergruppen aufweisender Polyglykoläther
DE2221756B2 (de)	1979-10-18	Verfahren zur Herstellung von lösungsmittelbeständigen, lichtechten, knick- und reibfesten Polyurethanüberzügen auf textlien Substraten, Leder oder Kunstleder oder von Folien
DE60017094T2 (de)	2006-04-27	Verfahren zur Herstellung einer wässrigen Dispersion eines anionischen Polyurethanes, die keine flüchtingen tertriären Amine enthält
EP0150803B1 (de)	1988-06-15	Haftungsvermittelnde Zusätze enthaltende PVC-Plastisole für Beschichtungszwecke und ihre Verwendung
EP0065688B1 (de)	1985-04-10	Verfahren zur Herstellung von Lösungsmittelarmen, hitzehärtbaren Polyurethan-Reaktivbeschichtungsmassen und ihre Verwendung in Direkt- und Umkehr-Beschichtungsverfahren
DE1282962B (de)	1968-11-14	Verfahren zur Herstellung waessriger sedimentierender redispergierbaren Dispersionen vernetzter, Harnstoffgruppe aufweisender Polyadditionsprodukte
DE2633396A1 (de)	1977-02-17	Verfahren zur herstellung einer anionischen waessrigen polyurethanemulsion
EP0208908A1 (de)	1987-01-21	Ionisch modifizierte PUR-Streichpasten und ihre Verwendung
EP0006174A1 (de)	1980-01-09	Verfahren zur Herstellung von Überzügen aus Polyurethanharnstoff-Elastomeren