JPS6238370B2 - - Google Patents
Info
- Publication number
- JPS6238370B2 JPS6238370B2 JP60160405A JP16040585A JPS6238370B2 JP S6238370 B2 JPS6238370 B2 JP S6238370B2 JP 60160405 A JP60160405 A JP 60160405A JP 16040585 A JP16040585 A JP 16040585A JP S6238370 B2 JPS6238370 B2 JP S6238370B2
- Authority
- JP
- Japan
- Prior art keywords
- acid
- weight
- diacid
- proportion
- acids
- Prior art date
- Legal status (The legal status 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 status listed.)
- Expired
Links
- 229920006149 polyester-amide block copolymer Polymers 0.000 claims abstract description 24
- 239000000203 mixture Substances 0.000 claims abstract description 19
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 12
- 230000009477 glass transition Effects 0.000 claims abstract description 6
- 125000000524 functional group Chemical group 0.000 claims abstract description 5
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims abstract description 4
- 150000001735 carboxylic acids Chemical group 0.000 claims abstract 5
- 239000002253 acid Substances 0.000 claims description 34
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 20
- 239000000376 reactant Substances 0.000 claims description 16
- 150000007513 acids Chemical class 0.000 claims description 11
- 150000005690 diesters Chemical class 0.000 claims description 8
- 150000003951 lactams Chemical class 0.000 claims description 8
- 229920002647 polyamide Polymers 0.000 claims description 8
- 239000004952 Polyamide Substances 0.000 claims description 7
- 150000001413 amino acids Chemical class 0.000 claims description 7
- 238000004519 manufacturing process Methods 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 6
- 229920000728 polyester Polymers 0.000 claims description 6
- 125000001931 aliphatic group Chemical group 0.000 claims description 5
- 150000001875 compounds Chemical class 0.000 claims description 5
- 229920006039 crystalline polyamide Polymers 0.000 claims description 5
- -1 aliphatic diamine Chemical class 0.000 claims description 4
- 125000003118 aryl group Chemical group 0.000 claims description 4
- 229920000909 polytetrahydrofuran Polymers 0.000 claims description 3
- 150000002009 diols Chemical class 0.000 claims description 2
- ZWVMLYRJXORSEP-LURJTMIESA-N (2s)-hexane-1,2,6-triol Chemical compound OCCCC[C@H](O)CO ZWVMLYRJXORSEP-LURJTMIESA-N 0.000 claims 1
- 150000002148 esters Chemical class 0.000 abstract description 7
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 abstract 2
- 239000000178 monomer Substances 0.000 abstract 2
- 150000001991 dicarboxylic acids Chemical class 0.000 abstract 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 28
- 229910052757 nitrogen Inorganic materials 0.000 description 19
- 239000000539 dimer Substances 0.000 description 15
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexamethylene diamine Natural products NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 15
- 150000001408 amides Chemical class 0.000 description 11
- 229920000642 polymer Polymers 0.000 description 11
- 239000000047 product Substances 0.000 description 11
- 238000003756 stirring Methods 0.000 description 9
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 8
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 8
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 6
- GIMXAEZBXRIECN-UHFFFAOYSA-J 2-hydroxyacetate;titanium(4+) Chemical compound [Ti+4].OCC([O-])=O.OCC([O-])=O.OCC([O-])=O.OCC([O-])=O GIMXAEZBXRIECN-UHFFFAOYSA-J 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 5
- 125000000896 monocarboxylic acid group Chemical group 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 235000014113 dietary fatty acids Nutrition 0.000 description 4
- 239000000194 fatty acid Substances 0.000 description 4
- 229930195729 fatty acid Natural products 0.000 description 4
- 150000004665 fatty acids Chemical class 0.000 description 4
- 238000005259 measurement Methods 0.000 description 4
- 238000002844 melting Methods 0.000 description 4
- 230000008018 melting Effects 0.000 description 4
- 238000006068 polycondensation reaction Methods 0.000 description 4
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 3
- 238000005886 esterification reaction Methods 0.000 description 3
- 238000010926 purge Methods 0.000 description 3
- 229910001220 stainless steel Inorganic materials 0.000 description 3
- 239000010935 stainless steel Substances 0.000 description 3
- 229920002725 thermoplastic elastomer Polymers 0.000 description 3
- YWWVWXASSLXJHU-AATRIKPKSA-N (9E)-tetradecenoic acid Chemical compound CCCC\C=C\CCCCCCCC(O)=O YWWVWXASSLXJHU-AATRIKPKSA-N 0.000 description 2
- PBLZLIFKVPJDCO-UHFFFAOYSA-N 12-aminododecanoic acid Chemical compound NCCCCCCCCCCCC(O)=O PBLZLIFKVPJDCO-UHFFFAOYSA-N 0.000 description 2
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 2
- SLXKOJJOQWFEFD-UHFFFAOYSA-N 6-aminohexanoic acid Chemical compound NCCCCCC(O)=O SLXKOJJOQWFEFD-UHFFFAOYSA-N 0.000 description 2
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 229960002684 aminocaproic acid Drugs 0.000 description 2
- 238000007707 calorimetry Methods 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- GHVNFZFCNZKVNT-UHFFFAOYSA-N decanoic acid Chemical compound CCCCCCCCCC(O)=O GHVNFZFCNZKVNT-UHFFFAOYSA-N 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- UKMSUNONTOPOIO-UHFFFAOYSA-N docosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- VKOBVWXKNCXXDE-UHFFFAOYSA-N icosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCC(O)=O VKOBVWXKNCXXDE-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- RLSSMJSEOOYNOY-UHFFFAOYSA-N m-cresol Chemical compound CC1=CC=CC(O)=C1 RLSSMJSEOOYNOY-UHFFFAOYSA-N 0.000 description 2
- 239000012299 nitrogen atmosphere Substances 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
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-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
- WLJVNTCWHIRURA-UHFFFAOYSA-N pimelic acid Chemical compound OC(=O)CCCCCC(O)=O WLJVNTCWHIRURA-UHFFFAOYSA-N 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000005297 pyrex Substances 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- TYFQFVWCELRYAO-UHFFFAOYSA-N suberic acid Chemical compound OC(=O)CCCCCCC(O)=O TYFQFVWCELRYAO-UHFFFAOYSA-N 0.000 description 2
- MRERMGPPCLQIPD-NBVRZTHBSA-N (3beta,5alpha,9alpha,22E,24R)-3,5,9-Trihydroxy-23-methylergosta-7,22-dien-6-one Chemical compound C1C(O)CCC2(C)C(CCC3(C(C(C)/C=C(\C)C(C)C(C)C)CCC33)C)(O)C3=CC(=O)C21O MRERMGPPCLQIPD-NBVRZTHBSA-N 0.000 description 1
- 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 1
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-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
- GUOSQNAUYHMCRU-UHFFFAOYSA-N 11-Aminoundecanoic acid Chemical compound NCCCCCCCCCCC(O)=O GUOSQNAUYHMCRU-UHFFFAOYSA-N 0.000 description 1
- ZONJATNKKGGVSU-UHFFFAOYSA-N 14-methylpentadecanoic acid Chemical compound CC(C)CCCCCCCCCCCCC(O)=O ZONJATNKKGGVSU-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- VWPQCOZMXULHDM-UHFFFAOYSA-N 9-aminononanoic acid Chemical compound NCCCCCCCCC(O)=O VWPQCOZMXULHDM-UHFFFAOYSA-N 0.000 description 1
- FKLSONDBCYHMOQ-UHFFFAOYSA-N 9E-dodecenoic acid Natural products CCC=CCCCCCCCC(O)=O FKLSONDBCYHMOQ-UHFFFAOYSA-N 0.000 description 1
- YWWVWXASSLXJHU-UHFFFAOYSA-N 9E-tetradecenoic acid Natural products CCCCC=CCCCCCCCC(O)=O YWWVWXASSLXJHU-UHFFFAOYSA-N 0.000 description 1
- 235000021357 Behenic acid Nutrition 0.000 description 1
- 239000004135 Bone phosphate Substances 0.000 description 1
- 239000005632 Capric acid (CAS 334-48-5) Substances 0.000 description 1
- 239000005635 Caprylic acid (CAS 124-07-2) Substances 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 239000004831 Hot glue Substances 0.000 description 1
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- JHWNWJKBPDFINM-UHFFFAOYSA-N Laurolactam Chemical compound O=C1CCCCCCCCCCCN1 JHWNWJKBPDFINM-UHFFFAOYSA-N 0.000 description 1
- 239000002841 Lewis acid Substances 0.000 description 1
- OYHQOLUKZRVURQ-HZJYTTRNSA-N Linoleic acid Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(O)=O OYHQOLUKZRVURQ-HZJYTTRNSA-N 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-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
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 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
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 125000002723 alicyclic group Chemical group 0.000 description 1
- 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 1
- 235000020661 alpha-linolenic acid Nutrition 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- JFCQEDHGNNZCLN-UHFFFAOYSA-N anhydrous glutaric acid Natural products OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 description 1
- CJYXCQLOZNIMFP-UHFFFAOYSA-N azocan-2-one Chemical compound O=C1CCCCCCN1 CJYXCQLOZNIMFP-UHFFFAOYSA-N 0.000 description 1
- YDLSUFFXJYEVHW-UHFFFAOYSA-N azonan-2-one Chemical compound O=C1CCCCCCCN1 YDLSUFFXJYEVHW-UHFFFAOYSA-N 0.000 description 1
- 229940116226 behenic acid Drugs 0.000 description 1
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 description 1
- 235000019445 benzyl alcohol Nutrition 0.000 description 1
- 230000015572 biosynthetic process Effects 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
- 125000002843 carboxylic acid group Chemical group 0.000 description 1
- KJDZDTDNIULJBE-QXMHVHEDSA-N cetoleic acid Chemical compound CCCCCCCCCC\C=C/CCCCCCCCCC(O)=O KJDZDTDNIULJBE-QXMHVHEDSA-N 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- XZJZNZATFHOMSJ-KTKRTIGZSA-N cis-3-dodecenoic acid Chemical compound CCCCCCCC\C=C/CC(O)=O XZJZNZATFHOMSJ-KTKRTIGZSA-N 0.000 description 1
- SECPZKHBENQXJG-UHFFFAOYSA-N cis-palmitoleic acid Natural products CCCCCCC=CCCCCCCCC(O)=O SECPZKHBENQXJG-UHFFFAOYSA-N 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000004455 differential thermal analysis Methods 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- GZZPOFFXKUVNSW-UHFFFAOYSA-N dodec-11-enoic acid Chemical compound OC(=O)CCCCCCCCCC=C GZZPOFFXKUVNSW-UHFFFAOYSA-N 0.000 description 1
- IQLUYYHUNSSHIY-HZUMYPAESA-N eicosatetraenoic acid Chemical compound CCCCCCCCCCC\C=C\C=C\C=C\C=C\C(O)=O IQLUYYHUNSSHIY-HZUMYPAESA-N 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000000806 elastomer Substances 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 238000005194 fractionation Methods 0.000 description 1
- LQJBNNIYVWPHFW-QXMHVHEDSA-N gadoleic acid Chemical compound CCCCCCCCCC\C=C/CCCCCCCC(O)=O LQJBNNIYVWPHFW-QXMHVHEDSA-N 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 150000007517 lewis acids Chemical class 0.000 description 1
- 235000020778 linoleic acid Nutrition 0.000 description 1
- OYHQOLUKZRVURQ-IXWMQOLASA-N linoleic acid Natural products CCCCC\C=C/C\C=C\CCCCCCCC(O)=O OYHQOLUKZRVURQ-IXWMQOLASA-N 0.000 description 1
- 229960004488 linolenic acid Drugs 0.000 description 1
- KQQKGWQCNNTQJW-UHFFFAOYSA-N linolenic acid Natural products CC=CCCC=CCC=CCCCCCCCC(O)=O KQQKGWQCNNTQJW-UHFFFAOYSA-N 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-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
- 229960002446 octanoic acid Drugs 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 229920002959 polymer blend Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 235000003441 saturated fatty acids Nutrition 0.000 description 1
- 150000004671 saturated fatty acids Chemical class 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- TUNFSRHWOTWDNC-HKGQFRNVSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCC[14C](O)=O TUNFSRHWOTWDNC-HKGQFRNVSA-N 0.000 description 1
- 238000012932 thermodynamic analysis Methods 0.000 description 1
- 238000004448 titration Methods 0.000 description 1
- IWPOSDLLFZKGOW-AATRIKPKSA-N trans-beta-octenoic acid Chemical compound CCCC\C=C\CC(O)=O IWPOSDLLFZKGOW-AATRIKPKSA-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
- C08G69/00—Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
- C08G69/44—Polyester-amides
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Polyamides (AREA)
- Polyesters Or Polycarbonates (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Silicon Polymers (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Materials For Medical Uses (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR79/30650 | 1979-12-10 | ||
| FR7930650A FR2471394A1 (fr) | 1979-12-10 | 1979-12-10 | Copolyesteramides souples a basse temperature |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6169831A JPS6169831A (ja) | 1986-04-10 |
| JPS6238370B2 true JPS6238370B2 (en, 2012) | 1987-08-18 |
Family
ID=9232761
Family Applications (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP17271080A Granted JPS5692920A (en) | 1979-12-10 | 1980-12-09 | Copolyester amide flexible at low temperature |
| JP60160406A Granted JPS6169832A (ja) | 1979-12-10 | 1985-07-22 | 低温において柔軟性であるコポリエステルアミド |
| JP60160405A Granted JPS6169831A (ja) | 1979-12-10 | 1985-07-22 | 低温において柔軟性であるコポリエステルアミド |
Family Applications Before (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP17271080A Granted JPS5692920A (en) | 1979-12-10 | 1980-12-09 | Copolyester amide flexible at low temperature |
| JP60160406A Granted JPS6169832A (ja) | 1979-12-10 | 1985-07-22 | 低温において柔軟性であるコポリエステルアミド |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US4343743A (en, 2012) |
| EP (1) | EP0030904B1 (en, 2012) |
| JP (3) | JPS5692920A (en, 2012) |
| AT (1) | ATE12397T1 (en, 2012) |
| BR (1) | BR8008041A (en, 2012) |
| CA (1) | CA1147883A (en, 2012) |
| DE (1) | DE3070400D1 (en, 2012) |
| DK (1) | DK160769C (en, 2012) |
| ES (1) | ES8203928A1 (en, 2012) |
| FI (1) | FI66885C (en, 2012) |
| FR (1) | FR2471394A1 (en, 2012) |
| GR (1) | GR71621B (en, 2012) |
| IE (1) | IE50612B1 (en, 2012) |
Families Citing this family (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4482587A (en) * | 1983-05-19 | 1984-11-13 | Eastman Kodak Company | Bonding compositions and shaped articles utilizing the bonding compositions |
| US4482588A (en) * | 1983-05-19 | 1984-11-13 | Eastman Kodak Company | Bonding compositions and shaped articles utilizing the bonding compositions |
| US4485233A (en) * | 1984-02-27 | 1984-11-27 | Union Camp Corporation | Poly(ester-amide) hot-melt adhesives |
| US4656242A (en) * | 1985-06-07 | 1987-04-07 | Henkel Corporation | Poly(ester-amide) compositions |
| US4816551A (en) * | 1985-11-19 | 1989-03-28 | Mi Drilling Fluids Company | Oil based drilling fluids |
| US4722963A (en) * | 1985-12-20 | 1988-02-02 | Henkel Corporation | Aromatic dicarboxylic acid polyamide having acid value greater than 35 |
| US4611051A (en) * | 1985-12-31 | 1986-09-09 | Union Camp Corporation | Novel poly(ester-amide) hot-melt adhesives |
| JPH0791377B2 (ja) * | 1986-04-17 | 1995-10-04 | ヘンケル・コ−ポレイシヨン | 水溶性を改良したポリアミド樹脂 |
| ES2020299B3 (es) | 1986-12-19 | 1991-08-01 | Ciba-Geigy Ag | Resinas epoxidicas con contenido de poliester sobre base de polialquilenglicol. |
| US5091494A (en) * | 1990-07-30 | 1992-02-25 | Akademie Der Wissenschaften Der Ddr | Copolyester amides, and method for making |
| KR960704978A (ko) * | 1993-09-28 | 1996-10-09 | 메리 베스 엘리어트 | 폴리아미드 수지를 함유하는 경화성 접착제 조성물(Curable Adhesive Compositions Containing Polyamide Resins) |
| NL1003459C2 (nl) * | 1996-06-28 | 1998-01-07 | Univ Twente | Copoly(ester-amides) en copoly(ester-urethanen). |
| GB0111794D0 (en) | 2001-05-15 | 2001-07-04 | Ici Plc | Polyamide copolymer |
| US6908887B2 (en) * | 2002-08-22 | 2005-06-21 | Halliburton Energy Services, Inc. | Suspending agent |
| EP1596875A4 (en) * | 2003-02-14 | 2006-04-05 | Inolex Investment Corp | TERTIARY AMINE FUNCTIONAL COMPLEX POLYESTER POLYMERS AND MANUFACTURING AND USE METHOD |
| US8450447B2 (en) * | 2007-03-14 | 2013-05-28 | Dow Global Technologies Llc | Copolyesteramides with decreased perfection of the amide sequence |
| US8784988B2 (en) * | 2008-11-25 | 2014-07-22 | Dow Global Technologies Llc | Polymer inorganic-particulate composite fibers |
| JP5671765B2 (ja) * | 2009-04-20 | 2015-02-18 | ディーエスエム アイピー アセッツ ビー．ブイ． | 柔軟なポリマー |
| WO2011073308A1 (en) * | 2009-12-16 | 2011-06-23 | Dsm Ip Assets B.V. | Thermoplastic polymer for plastic components for pumps |
| BR112012029451A2 (pt) * | 2010-05-19 | 2017-03-07 | Mitsubishi Gas Chemical Co | composto de amida de poliéster |
| EP2892966A4 (en) | 2011-09-06 | 2016-06-15 | Flint Trading Inc | Antifoaming agents for hot-melt adhesives |
| CN113754835B (zh) * | 2021-08-11 | 2024-03-12 | 东莞市比翼新材料科技有限公司 | 油脂基改性不饱和聚酯树脂及其制备方法 |
| JP7160426B1 (ja) * | 2022-08-31 | 2022-10-25 | 竹本油脂株式会社 | 合成繊維用処理剤及び合成繊維 |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR1252419A (fr) * | 1959-03-28 | 1961-01-27 | Bayer Ag | Procédé de préparation de liants esters thixotropiques |
| DE1445305A1 (de) * | 1960-08-24 | 1968-11-14 | Coates Brothers & Company Ltd | Verfahren zum Herstellen thixotroper Materialien |
| FR1416456A (fr) * | 1964-09-17 | 1965-11-05 | Gen Mills Inc | Nouvelles compositions de copolymères de polyamides-poly |
| FR1547058A (fr) * | 1966-12-13 | 1968-11-22 | Schering Ag | Résines de poly-esteramides |
| DE1645440B2 (de) * | 1966-12-13 | 1976-05-06 | Schering Ag, 1000 Berlin Und 4619 Bergkamen | Neue haertbare ungesaettigte polyesteramidharzmassen |
| GB1252282A (en, 2012) * | 1968-06-07 | 1971-11-03 | ||
| US3637551A (en) * | 1969-06-11 | 1972-01-25 | Du Pont | Melt-condensed polyamide interpolymer adhesives |
| US3650999A (en) * | 1970-06-15 | 1972-03-21 | Monsanto Co | Poly(ester-amide) block copolymer hot melt adhesives |
| DK144302C (da) * | 1975-07-31 | 1982-07-05 | Schering Ag | Polyamidsmelteklaebemiddel til klaebning af tekstiler |
| DE2534845A1 (de) * | 1975-08-05 | 1977-02-10 | Schering Ag | Druckverfahren und dafuer geeignete schmelzdruckfarben |
| US4218351A (en) * | 1978-07-17 | 1980-08-19 | Minnesota Mining And Manufacturing Company | Impact resistant, thermoplastic polyamides |
-
1979
- 1979-12-10 FR FR7930650A patent/FR2471394A1/fr active Granted
-
1980
- 1980-12-05 US US06/213,472 patent/US4343743A/en not_active Expired - Lifetime
- 1980-12-05 GR GR63591A patent/GR71621B/el unknown
- 1980-12-09 EP EP80420137A patent/EP0030904B1/fr not_active Expired
- 1980-12-09 FI FI803824A patent/FI66885C/fi not_active IP Right Cessation
- 1980-12-09 ES ES497542A patent/ES8203928A1/es not_active Expired
- 1980-12-09 JP JP17271080A patent/JPS5692920A/ja active Granted
- 1980-12-09 CA CA000366446A patent/CA1147883A/fr not_active Expired
- 1980-12-09 AT AT80420137T patent/ATE12397T1/de not_active IP Right Cessation
- 1980-12-09 IE IE2577/80A patent/IE50612B1/en not_active IP Right Cessation
- 1980-12-09 DK DK524580A patent/DK160769C/da not_active IP Right Cessation
- 1980-12-09 DE DE8080420137T patent/DE3070400D1/de not_active Expired
- 1980-12-10 BR BR8008041A patent/BR8008041A/pt unknown
-
1985
- 1985-07-22 JP JP60160406A patent/JPS6169832A/ja active Granted
- 1985-07-22 JP JP60160405A patent/JPS6169831A/ja active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| IE802577L (en) | 1981-06-10 |
| FI66885B (fi) | 1984-08-31 |
| DK160769B (da) | 1991-04-15 |
| JPS6169831A (ja) | 1986-04-10 |
| ES497542A0 (es) | 1982-04-16 |
| US4343743A (en) | 1982-08-10 |
| DE3070400D1 (en) | 1985-05-02 |
| IE50612B1 (en) | 1986-05-28 |
| JPS5692920A (en) | 1981-07-28 |
| JPS6136858B2 (en, 2012) | 1986-08-20 |
| EP0030904A1 (fr) | 1981-06-24 |
| FI803824L (fi) | 1981-06-11 |
| DK160769C (da) | 1991-09-30 |
| GR71621B (en, 2012) | 1983-06-20 |
| JPS6310168B2 (en, 2012) | 1988-03-04 |
| FI66885C (fi) | 1984-12-10 |
| FR2471394B1 (en, 2012) | 1985-05-17 |
| ES8203928A1 (es) | 1982-04-16 |
| EP0030904B1 (fr) | 1985-03-27 |
| CA1147883A (fr) | 1983-06-07 |
| FR2471394A1 (fr) | 1981-06-19 |
| ATE12397T1 (de) | 1985-04-15 |
| JPS6169832A (ja) | 1986-04-10 |
| BR8008041A (pt) | 1981-06-23 |
| DK524580A (da) | 1981-06-11 |
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