NO771087L - Flytende, reaktive polyamidprodukter. - Google Patents

Flytende, reaktive polyamidprodukter.

Info

Publication number: NO771087L
Authority: NO; Norway
Prior art keywords: acid; weight; less; amine; product
Prior art date: 1976-03-29

Application number

NO771087A

Other languages

English (en)

Norwegian (no)

Inventor

Hubert J Sharkey

Robert Allan Winstel

Original Assignee

Unilever Emery

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.)

1976-03-29

Filing date

1977-03-28

Publication date

1977-09-30

1977-03-28 Application filed by Unilever Emery filed Critical Unilever Emery

1977-09-30 Publication of NO771087L publication Critical patent/NO771087L/no

Links

229920002647 polyamide Polymers 0.000 title claims description 47
239000004952 Polyamide Substances 0.000 title claims description 46
239000007788 liquid Substances 0.000 title claims description 28
150000001412 amines Chemical class 0.000 claims description 67
239000002253 acid Substances 0.000 claims description 59
239000000047 product Substances 0.000 claims description 36
NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 claims description 28
150000007513 acids Chemical class 0.000 claims description 22
125000004432 carbon atom Chemical group C* 0.000 claims description 18
150000007519 polyprotic acids Polymers 0.000 claims description 18
238000000034 method Methods 0.000 claims description 16
235000014113 dietary fatty acids Nutrition 0.000 claims description 14
239000000194 fatty acid Substances 0.000 claims description 14
229930195729 fatty acid Natural products 0.000 claims description 14
150000004665 fatty acids Chemical class 0.000 claims description 14
-1 heterocyclic amine Chemical class 0.000 claims description 12
JZUHIOJYCPIVLQ-UHFFFAOYSA-N 2-methylpentane-1,5-diamine Chemical compound NCC(C)CCCN JZUHIOJYCPIVLQ-UHFFFAOYSA-N 0.000 claims description 10
125000001931 aliphatic group Chemical group 0.000 claims description 8
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 8
239000000539 dimer Substances 0.000 claims description 8
150000002763 monocarboxylic acids Chemical class 0.000 claims description 8
BTGRAWJCKBQKAO-UHFFFAOYSA-N adiponitrile Chemical compound N#CCCCCC#N BTGRAWJCKBQKAO-UHFFFAOYSA-N 0.000 claims description 7
239000006227 byproduct Substances 0.000 claims description 7
QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 6
OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 5
SSJXIUAHEKJCMH-UHFFFAOYSA-N cyclohexane-1,2-diamine Chemical compound NC1CCCCC1N SSJXIUAHEKJCMH-UHFFFAOYSA-N 0.000 claims description 5
SRGQQZYVZFJYHJ-UHFFFAOYSA-N 2-(aminomethyl)cyclopentan-1-amine Chemical compound NCC1CCCC1N SRGQQZYVZFJYHJ-UHFFFAOYSA-N 0.000 claims description 4
RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 claims description 4
238000005984 hydrogenation reaction Methods 0.000 claims description 4
230000007935 neutral effect Effects 0.000 claims description 4
VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 claims description 2
125000003118 aryl group Chemical group 0.000 claims description 2
RTWNYYOXLSILQN-UHFFFAOYSA-N methanediamine Chemical compound NCN RTWNYYOXLSILQN-UHFFFAOYSA-N 0.000 claims description 2
239000003921 oil Substances 0.000 claims description 2
239000013638 trimer Substances 0.000 claims description 2
239000007795 chemical reaction product Substances 0.000 claims 1
230000000379 polymerizing effect Effects 0.000 claims 1
239000000344 soap Substances 0.000 claims 1
239000000203 mixture Substances 0.000 description 17
238000006243 chemical reaction Methods 0.000 description 13
239000011541 reaction mixture Substances 0.000 description 10
150000001732 carboxylic acid derivatives Chemical class 0.000 description 9
150000004985 diamines Chemical class 0.000 description 8
238000004519 manufacturing process Methods 0.000 description 7
229920005989 resin Polymers 0.000 description 7
239000011347 resin Substances 0.000 description 7
XBPCUCUWBYBCDP-UHFFFAOYSA-N Dicyclohexylamine Chemical compound C1CCCCC1NC1CCCCC1 XBPCUCUWBYBCDP-UHFFFAOYSA-N 0.000 description 6
ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 6
ZQPPMHVWECSIRJ-MDZDMXLPSA-N elaidic acid Chemical compound CCCCCCCC\C=C\CCCCCCCC(O)=O ZQPPMHVWECSIRJ-MDZDMXLPSA-N 0.000 description 6
QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 6
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 5
LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 5
QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 5
239000005642 Oleic acid Substances 0.000 description 5
238000004821 distillation Methods 0.000 description 5
OYHQOLUKZRVURQ-HZJYTTRNSA-N Linoleic acid Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(O)=O OYHQOLUKZRVURQ-HZJYTTRNSA-N 0.000 description 4
238000010438 heat treatment Methods 0.000 description 4
229930195733 hydrocarbon Natural products 0.000 description 4
235000020778 linoleic acid Nutrition 0.000 description 4
OYHQOLUKZRVURQ-IXWMQOLASA-N linoleic acid Natural products CCCCC\C=C/C\C=C\CCCCCCCC(O)=O OYHQOLUKZRVURQ-IXWMQOLASA-N 0.000 description 4
239000000463 material Substances 0.000 description 4
238000002156 mixing Methods 0.000 description 4
229920000768 polyamine Polymers 0.000 description 4
229920006345 thermoplastic polyamide Polymers 0.000 description 4
MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
239000011230 binding agent Substances 0.000 description 3
IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 3
239000012263 liquid product Substances 0.000 description 3
229910052751 metal Inorganic materials 0.000 description 3
239000002184 metal Substances 0.000 description 3
230000003647 oxidation Effects 0.000 description 3
238000007254 oxidation reaction Methods 0.000 description 3
239000000376 reactant Substances 0.000 description 3
235000021122 unsaturated fatty acids Nutrition 0.000 description 3
150000004670 unsaturated fatty acids Chemical class 0.000 description 3
OYHQOLUKZRVURQ-NTGFUMLPSA-N (9Z,12Z)-9,10,12,13-tetratritiooctadeca-9,12-dienoic acid Chemical compound C(CCCCCCC\C(=C(/C\C(=C(/CCCCC)\[3H])\[3H])\[3H])\[3H])(=O)O OYHQOLUKZRVURQ-NTGFUMLPSA-N 0.000 description 2
XDOFQFKRPWOURC-UHFFFAOYSA-N 16-methylheptadecanoic acid Chemical compound CC(C)CCCCCCCCCCCCCCC(O)=O XDOFQFKRPWOURC-UHFFFAOYSA-N 0.000 description 2
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
DPUOLQHDNGRHBS-UHFFFAOYSA-N Brassidinsaeure Natural products CCCCCCCCC=CCCCCCCCCCCCC(O)=O DPUOLQHDNGRHBS-UHFFFAOYSA-N 0.000 description 2
239000004215 Carbon black (E152) Substances 0.000 description 2
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 2
WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
229910000318 alkali metal phosphate Inorganic materials 0.000 description 2
DTOSIQBPPRVQHS-PDBXOOCHSA-N alpha-linolenic acid Chemical compound CC\C=C/C\C=C/C\C=C/CCCCCCCC(O)=O DTOSIQBPPRVQHS-PDBXOOCHSA-N 0.000 description 2
235000020661 alpha-linolenic acid Nutrition 0.000 description 2
VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 2
125000003277 amino group Chemical group 0.000 description 2
IMUDHTPIFIBORV-UHFFFAOYSA-N aminoethylpiperazine Chemical compound NCCN1CCNCC1 IMUDHTPIFIBORV-UHFFFAOYSA-N 0.000 description 2
150000001735 carboxylic acids Chemical class 0.000 description 2
238000009903 catalytic hydrogenation reaction Methods 0.000 description 2
150000001875 compounds Chemical class 0.000 description 2
238000007796 conventional method Methods 0.000 description 2
POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
239000003822 epoxy resin Substances 0.000 description 2
150000002430 hydrocarbons Chemical class 0.000 description 2
229960004488 linolenic acid Drugs 0.000 description 2
KQQKGWQCNNTQJW-UHFFFAOYSA-N linolenic acid Natural products CC=CCCC=CCC=CCCCCCCCC(O)=O KQQKGWQCNNTQJW-UHFFFAOYSA-N 0.000 description 2
BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 2
FBUKVWPVBMHYJY-UHFFFAOYSA-N nonanoic acid Chemical compound CCCCCCCCC(O)=O FBUKVWPVBMHYJY-UHFFFAOYSA-N 0.000 description 2
SECPZKHBENQXJG-FPLPWBNLSA-N palmitoleic acid Chemical compound CCCCCC\C=C/CCCCCCCC(O)=O SECPZKHBENQXJG-FPLPWBNLSA-N 0.000 description 2
229920000647 polyepoxide Polymers 0.000 description 2
238000006116 polymerization reaction Methods 0.000 description 2
150000003839 salts Chemical class 0.000 description 2
239000007787 solid Substances 0.000 description 2
238000003756 stirring Methods 0.000 description 2
125000001424 substituent group Chemical group 0.000 description 2
239000003784 tall oil Substances 0.000 description 2
OBETXYAYXDNJHR-SSDOTTSWSA-M (2r)-2-ethylhexanoate Chemical compound CCCC[C@@H](CC)C([O-])=O OBETXYAYXDNJHR-SSDOTTSWSA-M 0.000 description 1
CFQZKFWQLAHGSL-FNTYJUCDSA-N (3e,5e,7e,9e,11e,13e,15e,17e)-18-[(3e,5e,7e,9e,11e,13e,15e,17e)-18-[(3e,5e,7e,9e,11e,13e,15e)-octadeca-3,5,7,9,11,13,15,17-octaenoyl]oxyoctadeca-3,5,7,9,11,13,15,17-octaenoyl]oxyoctadeca-3,5,7,9,11,13,15,17-octaenoic acid Chemical compound OC(=O)C\C=C\C=C\C=C\C=C\C=C\C=C\C=C\C=C\OC(=O)C\C=C\C=C\C=C\C=C\C=C\C=C\C=C\C=C\OC(=O)C\C=C\C=C\C=C\C=C\C=C\C=C\C=C\C=C CFQZKFWQLAHGSL-FNTYJUCDSA-N 0.000 description 1
XBTRYWRVOBZSGM-UHFFFAOYSA-N (4-methylphenyl)methanediamine Chemical compound CC1=CC=C(C(N)N)C=C1 XBTRYWRVOBZSGM-UHFFFAOYSA-N 0.000 description 1
CUXYLFPMQMFGPL-UHFFFAOYSA-N (9Z,11E,13E)-9,11,13-Octadecatrienoic acid Natural products CCCCC=CC=CC=CCCCCCCCC(O)=O CUXYLFPMQMFGPL-UHFFFAOYSA-N 0.000 description 1
RTBFRGCFXZNCOE-UHFFFAOYSA-N 1-methylsulfonylpiperidin-4-one Chemical compound CS(=O)(=O)N1CCC(=O)CC1 RTBFRGCFXZNCOE-UHFFFAOYSA-N 0.000 description 1
VYZPXGMSAOCYOL-UHFFFAOYSA-N 2-[2-(2-aminoethyl)phenyl]ethanamine Chemical compound NCCC1=CC=CC=C1CCN VYZPXGMSAOCYOL-UHFFFAOYSA-N 0.000 description 1
OSWAHEFGQRSIIJ-UHFFFAOYSA-N 2-formyloctadecanoic acid Chemical compound CCCCCCCCCCCCCCCCC(C=O)C(O)=O OSWAHEFGQRSIIJ-UHFFFAOYSA-N 0.000 description 1
MVDKKZZVTWHVMC-UHFFFAOYSA-N 2-hexadecylpropanedioic acid Chemical class CCCCCCCCCCCCCCCCC(C(O)=O)C(O)=O MVDKKZZVTWHVMC-UHFFFAOYSA-N 0.000 description 1
WDHJMKYIJWJQLY-UHFFFAOYSA-N 2-nonyldecanedioic acid Chemical compound CCCCCCCCCC(C(O)=O)CCCCCCCC(O)=O WDHJMKYIJWJQLY-UHFFFAOYSA-N 0.000 description 1
IGMCTDOFLKWLPJ-UHFFFAOYSA-N 2-octylundecanedioic acid Chemical compound CCCCCCCCC(C(O)=O)CCCCCCCCC(O)=O IGMCTDOFLKWLPJ-UHFFFAOYSA-N 0.000 description 1
XUSNPFGLKGCWGN-UHFFFAOYSA-N 3-[4-(3-aminopropyl)piperazin-1-yl]propan-1-amine Chemical compound NCCCN1CCN(CCCN)CC1 XUSNPFGLKGCWGN-UHFFFAOYSA-N 0.000 description 1
UVLSCMIEPPWCHZ-UHFFFAOYSA-N 3-piperazin-1-ylpropan-1-amine Chemical compound NCCCN1CCNCC1 UVLSCMIEPPWCHZ-UHFFFAOYSA-N 0.000 description 1
ZILQRIKYRNQQDE-UHFFFAOYSA-N 4-(2-piperidin-4-ylethyl)piperidine Chemical compound C1CNCCC1CCC1CCNCC1 ZILQRIKYRNQQDE-UHFFFAOYSA-N 0.000 description 1
OXEZLYIDQPBCBB-UHFFFAOYSA-N 4-(3-piperidin-4-ylpropyl)piperidine Chemical compound C1CNCCC1CCCC1CCNCC1 OXEZLYIDQPBCBB-UHFFFAOYSA-N 0.000 description 1
YGIWTLULBLUFRJ-UHFFFAOYSA-N 4-(4-piperidin-4-ylbutyl)piperidine Chemical compound C1CNCCC1CCCCC1CCNCC1 YGIWTLULBLUFRJ-UHFFFAOYSA-N 0.000 description 1
239000004135 Bone phosphate Substances 0.000 description 1
235000013162 Cocos nucifera Nutrition 0.000 description 1
244000060011 Cocos nucifera Species 0.000 description 1
URXZXNYJPAJJOQ-UHFFFAOYSA-N Erucic acid Natural products CCCCCCC=CCCCCCCCCCCCC(O)=O URXZXNYJPAJJOQ-UHFFFAOYSA-N 0.000 description 1
239000005639 Lauric acid Substances 0.000 description 1
CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 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
235000021314 Palmitic acid Nutrition 0.000 description 1
235000021319 Palmitoleic acid Nutrition 0.000 description 1
239000005643 Pelargonic acid Substances 0.000 description 1
235000021355 Stearic acid Nutrition 0.000 description 1
KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
AAQCEEMRPKWTMP-UHFFFAOYSA-N [Br].CC1=CC=CC=C1O Chemical compound [Br].CC1=CC=CC=C1O AAQCEEMRPKWTMP-UHFFFAOYSA-N 0.000 description 1
239000003377 acid catalyst Substances 0.000 description 1
239000001361 adipic acid Substances 0.000 description 1
235000011037 adipic acid Nutrition 0.000 description 1
125000000217 alkyl group Chemical group 0.000 description 1
CUXYLFPMQMFGPL-SUTYWZMXSA-N all-trans-octadeca-9,11,13-trienoic acid Chemical compound CCCC\C=C\C=C\C=C\CCCCCCCC(O)=O CUXYLFPMQMFGPL-SUTYWZMXSA-N 0.000 description 1
OBETXYAYXDNJHR-UHFFFAOYSA-N alpha-ethylcaproic acid Natural products CCCCC(CC)C(O)=O OBETXYAYXDNJHR-UHFFFAOYSA-N 0.000 description 1
229910000147 aluminium phosphate Inorganic materials 0.000 description 1
125000004103 aminoalkyl group Chemical group 0.000 description 1
JFCQEDHGNNZCLN-UHFFFAOYSA-N anhydrous glutaric acid Natural products OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 description 1
ZSIQJIWKELUFRJ-UHFFFAOYSA-N azepane Chemical compound C1CCCNCC1 ZSIQJIWKELUFRJ-UHFFFAOYSA-N 0.000 description 1
238000009835 boiling Methods 0.000 description 1
KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
230000003197 catalytic effect Effects 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
SECPZKHBENQXJG-UHFFFAOYSA-N cis-palmitoleic acid Natural products CCCCCCC=CCCCCCCCC(O)=O SECPZKHBENQXJG-UHFFFAOYSA-N 0.000 description 1
239000007859 condensation product Substances 0.000 description 1
238000010276 construction Methods 0.000 description 1
150000001991 dicarboxylic acids Chemical class 0.000 description 1
ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
238000005538 encapsulation Methods 0.000 description 1
238000005265 energy consumption Methods 0.000 description 1
229920006334 epoxy coating Polymers 0.000 description 1
DPUOLQHDNGRHBS-KTKRTIGZSA-N erucic acid Chemical compound CCCCCCCC\C=C/CCCCCCCCCCCC(O)=O DPUOLQHDNGRHBS-KTKRTIGZSA-N 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
238000001914 filtration Methods 0.000 description 1
239000012467 final product Substances 0.000 description 1
238000005187 foaming Methods 0.000 description 1
239000011521 glass Substances 0.000 description 1
LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
239000011261 inert gas Substances 0.000 description 1
229910052500 inorganic mineral Inorganic materials 0.000 description 1
239000000543 intermediate Substances 0.000 description 1
150000002500 ions Chemical class 0.000 description 1
239000010985 leather Substances 0.000 description 1
239000004850 liquid epoxy resins (LERs) Substances 0.000 description 1
235000013310 margarine Nutrition 0.000 description 1
239000003264 margarine Substances 0.000 description 1
239000000155 melt Substances 0.000 description 1
239000011707 mineral Substances 0.000 description 1
WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
239000012299 nitrogen atmosphere Substances 0.000 description 1
GHLZUHZBBNDWHW-UHFFFAOYSA-N nonanamide Chemical compound CCCCCCCCC(N)=O GHLZUHZBBNDWHW-UHFFFAOYSA-N 0.000 description 1
QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
235000021313 oleic acid Nutrition 0.000 description 1
235000006408 oxalic acid Nutrition 0.000 description 1
238000005949 ozonolysis reaction Methods 0.000 description 1
150000002978 peroxides Chemical class 0.000 description 1
229920001568 phenolic resin Polymers 0.000 description 1
229920001084 poly(chloroprene) Polymers 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
150000003141 primary amines Chemical class 0.000 description 1
AOHJOMMDDJHIJH-UHFFFAOYSA-N propylenediamine Chemical compound CC(N)CN AOHJOMMDDJHIJH-UHFFFAOYSA-N 0.000 description 1
238000005086 pumping Methods 0.000 description 1
230000009257 reactivity Effects 0.000 description 1
238000010992 reflux Methods 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
229930195734 saturated hydrocarbon Natural products 0.000 description 1
150000003335 secondary amines Chemical group 0.000 description 1
239000008117 stearic acid Substances 0.000 description 1
239000000126 substance Substances 0.000 description 1
TUNFSRHWOTWDNC-HKGQFRNVSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCC[14C](O)=O TUNFSRHWOTWDNC-HKGQFRNVSA-N 0.000 description 1
238000004448 titration Methods 0.000 description 1
DPUOLQHDNGRHBS-MDZDMXLPSA-N trans-Brassidic acid Chemical compound CCCCCCCC\C=C\CCCCCCCCCCCC(O)=O DPUOLQHDNGRHBS-MDZDMXLPSA-N 0.000 description 1
229930195735 unsaturated hydrocarbon Natural products 0.000 description 1
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
229920002554 vinyl polymer Polymers 0.000 description 1
239000008096 xylene Substances 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
- C08L61/00—Compositions of condensation polymers of aldehydes or ketones; Compositions of derivatives of such polymers
- C08L61/04—Condensation polymers of aldehydes or ketones with phenols only
- C08L61/06—Condensation polymers of aldehydes or ketones with phenols only of aldehydes with phenols
- 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
- C08G69/00—Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
- C08G69/02—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L63/00—Compositions of epoxy resins; Compositions of derivatives of epoxy resins

Landscapes

Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Polyamides (AREA)

NO771087A 1976-03-29 1977-03-28 Flytende, reaktive polyamidprodukter. NO771087L (no)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US05/671,325 US4032549A (en)	1976-03-29	1976-03-29	Reactive liquid polyamides from amine residues

Publications (1)

Publication Number	Publication Date
NO771087L true NO771087L (no)	1977-09-30

Family

ID=24694044

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO771087A NO771087L (no)	1976-03-29	1977-03-28	Flytende, reaktive polyamidprodukter.

Country Status (12)

Country	Link
US (1)	US4032549A (fr)
AU (1)	AU2374277A (fr)
BE (1)	BE853008A (fr)
CA (1)	CA1097840A (fr)
DE (1)	DE2713956A1 (fr)
ES (1)	ES457376A1 (fr)
FR (1)	FR2346388A1 (fr)
NL (1)	NL7703414A (fr)
NO (1)	NO771087L (fr)
NZ (1)	NZ183732A (fr)
SE (1)	SE7703563L (fr)
ZA (1)	ZA771881B (fr)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US5354829A (en) *	1992-06-30	1994-10-11	Ppg Industries, Inc.	Silylated polyamine polymers and a method of treating fibers

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2767089A (en) *	1951-05-21	1956-10-16	Gen Mills Inc	Paper containing polyamide resins and process of producing same
US2886543A (en) *	1954-08-17	1959-05-12	Gen Mills Inc	Polyamide resin
US3242141A (en) *	1962-12-04	1966-03-22	Gen Mills Inc	Polyamide compositions from fatty dimer diamines
US3249629A (en) *	1963-03-15	1966-05-03	Gen Mills Inc	Polyamide of polymeric fat acids and 1, 3 or 1, 4-cyclohexane bis
US3396180A (en) *	1964-01-31	1968-08-06	Gen Mills Inc	Polyamide resin compositions of ethylene-diamine and fractionated polymeric fat acids
DE1745460B2 (de) *	1967-08-05	1976-07-15	Schering Ag, 1000 Berlin Und 4619 Bergkamen	Neue, haertbare ungesaettigte polyamidharzmassen
GB1282887A (en) *	1968-07-03	1972-07-26	Lubrizol Corp	Acylation of nitrogen-containing products
BE755035A (fr) *	1969-12-02	1971-02-01	Gen Mills Inc	Resine polyamide a base d'acides gras polymeres
US3622684A (en) *	1970-10-15	1971-11-23	Cole & Co Inc C W	Rotatable floor receptacle mounting unit
US3776865A (en) *	1972-05-30	1973-12-04	Gen Mills Chem Inc	Water-reducible acid terminated poly-meric fat acid polyamide resins useful as flexographic ink binders
US3892785A (en) *	1972-11-09	1975-07-01	Gen Mills Inc	Cross-linkable polyamides derived from polymeric fat acids

1976
- 1976-03-29 US US05/671,325 patent/US4032549A/en not_active Expired - Lifetime
1977
- 1977-03-28 SE SE7703563A patent/SE7703563L/xx unknown
- 1977-03-28 NO NO771087A patent/NO771087L/no unknown
- 1977-03-29 DE DE19772713956 patent/DE2713956A1/de active Pending
- 1977-03-29 FR FR7709425A patent/FR2346388A1/fr not_active Withdrawn
- 1977-03-29 ZA ZA00771881A patent/ZA771881B/xx unknown
- 1977-03-29 CA CA275,012A patent/CA1097840A/fr not_active Expired
- 1977-03-29 NZ NZ183732A patent/NZ183732A/xx unknown
- 1977-03-29 BE BE176226A patent/BE853008A/fr unknown
- 1977-03-29 AU AU23742/77A patent/AU2374277A/en not_active Expired
- 1977-03-29 NL NL7703414A patent/NL7703414A/xx not_active Application Discontinuation
- 1977-03-30 ES ES457376A patent/ES457376A1/es not_active Expired

Also Published As

Publication number	Publication date
CA1097840A (fr)	1981-03-17
ES457376A1 (es)	1978-02-16
BE853008A (fr)	1977-09-29
NL7703414A (nl)	1977-10-03
US4032549A (en)	1977-06-28
NZ183732A (en)	1978-07-10
SE7703563L (sv)	1977-09-30
DE2713956A1 (de)	1977-10-20
AU2374277A (en)	1978-10-05
FR2346388A1 (fr)	1977-10-28
ZA771881B (en)	1978-11-29

Publication	Publication Date	Title
US3236895A (en)	1966-02-22	Polyoxyalkylenepolyamines
US2450940A (en)	1948-10-12	Polyamides from polymeric fat acids
US2146210A (en)	1939-02-07	Synthetic resins
US2482761A (en)	1949-09-27	Polymerization of unsaturated fatty acids
US2355837A (en)	1944-08-15	Substituted glyoxalidines
US2306918A (en)	1942-12-29	Amine reaction product
US3127365A (en)	1964-03-31	Acrylic-modified amino polyamides
JPH08506369A (ja)	1996-07-09	接着促進剤
NO123198B (fr)	1971-10-11
EP0488650B1 (fr)	1996-02-07	Composition à base de résine, polyamide pour utilisation comme liant dans des encres stratifiables
US3133108A (en)	1964-05-12	Nitrogen coordinated silicon compounds
US2886543A (en)	1959-05-12	Polyamide resin
US3167554A (en)	1965-01-26	Piperazino alkylamides of polybasic carboxylic acids
NO150719B (no)	1984-08-27	Trijoderte baser og roentgenkontrastmidler inneholdende salter av slike baser
US2970971A (en)	1961-02-07	Composition of a monoepoxide modified polyamide and an epoxy resin
NO771087L (no)	1977-09-30	Flytende, reaktive polyamidprodukter.
EP0095347A2 (fr)	1983-11-30	Amido-amines aromatiques en tant que durcisseurs pour résines époxy
EP0195242B1 (fr)	1992-04-15	Polyamides ayant une solubilité dans l'eau et utilisables comme liants d'encres pour la flexographie ou la gravure
US4100112A (en)	1978-07-11	Process for the production of amine silicate compounds and their resinous condensation products
US2839549A (en)	1958-06-17	Bodied resinous polyamides
US2387976A (en)	1945-10-30	Method of forming carboxylic substituted amines
US2555111A (en)	1951-05-29	Polyamide resin from dimerized unsaturated fatty acids of natural fatty oils
US2324936A (en)	1943-07-20	Condensation of cyanocarboxylic acid with polyamine
US3010782A (en)	1961-11-28	Corrosion inhibiting method and composition
US3914195A (en)	1975-10-21	Preparation of solid polyamides useful as ink binders