CA2065185A1 - Compositions reticulables a base de resines, utiles comme adhesifs thermofusibles - Google Patents

Compositions reticulables a base de resines, utiles comme adhesifs thermofusibles

Info

Publication number: CA2065185A1
Authority: CA; Canada
Prior art keywords: composition; epoxy; diluent; resin; acid
Prior art date: 1990-10-30
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.): Abandoned

Application number

CA 2065185

Other languages

English (en)

Inventor

Charles R. Frihart

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Union Camp Corp

Original Assignee

Union Camp Corp

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.)

1990-10-30

Filing date

1992-04-06

Publication date

1993-02-10

1991-08-09 Priority claimed from US07/743,050 external-priority patent/US5296556A/en

1992-04-06 Application filed by Union Camp Corp filed Critical Union Camp Corp

1993-02-10 Publication of CA2065185A1 publication Critical patent/CA2065185A1/fr

Status Abandoned legal-status Critical Current

Links

239000011342 resin composition Substances 0.000 title claims abstract description 11
239000004831 Hot glue Substances 0.000 title claims abstract description 7
239000000203 mixture Substances 0.000 claims abstract description 82
229920006122 polyamide resin Polymers 0.000 claims abstract description 41
229920000647 polyepoxide Polymers 0.000 claims abstract description 41
239000003085 diluting agent Substances 0.000 claims abstract description 40
239000003822 epoxy resin Substances 0.000 claims abstract description 38
239000002253 acid Substances 0.000 claims abstract description 30
150000001412 amines Chemical class 0.000 claims abstract description 28
238000000034 method Methods 0.000 claims abstract description 24
125000003700 epoxy group Chemical group 0.000 claims abstract description 23
125000003277 amino group Chemical group 0.000 claims abstract description 15
230000002411 adverse Effects 0.000 claims abstract description 8
230000008569 process Effects 0.000 claims abstract description 6
229920001169 thermoplastic Polymers 0.000 claims abstract description 6
239000004416 thermosoftening plastic Substances 0.000 claims abstract description 6
239000004593 Epoxy Substances 0.000 claims description 24
239000000539 dimer Substances 0.000 claims description 17
GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 claims description 16
150000004985 diamines Chemical class 0.000 claims description 16
235000014113 dietary fatty acids Nutrition 0.000 claims description 16
150000004665 fatty acids Chemical class 0.000 claims description 16
239000000194 fatty acid Substances 0.000 claims description 15
229930195729 fatty acid Natural products 0.000 claims description 15
229920000768 polyamine Polymers 0.000 claims description 11
NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 claims description 8
OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 7
125000004432 carbon atom Chemical group C* 0.000 claims description 7
BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 claims description 7
150000002763 monocarboxylic acids Chemical class 0.000 claims description 6
PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 claims description 5
238000002156 mixing Methods 0.000 claims description 5
JZUHIOJYCPIVLQ-UHFFFAOYSA-N 2-methylpentane-1,5-diamine Chemical compound NCC(C)CCCN JZUHIOJYCPIVLQ-UHFFFAOYSA-N 0.000 claims description 4
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 4
239000007795 chemical reaction product Substances 0.000 claims description 4
125000004122 cyclic group Chemical group 0.000 claims description 4
239000000155 melt Substances 0.000 claims description 4
RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 claims description 3
GWFGDXZQZYMSMJ-UHFFFAOYSA-N Octadecansaeure-heptadecylester Natural products CCCCCCCCCCCCCCCCCOC(=O)CCCCCCCCCCCCCCCCC GWFGDXZQZYMSMJ-UHFFFAOYSA-N 0.000 claims description 3
150000001408 amides Chemical class 0.000 claims description 3
150000002148 esters Chemical class 0.000 claims description 3
238000004519 manufacturing process Methods 0.000 claims description 3
RKISUIUJZGSLEV-UHFFFAOYSA-N n-[2-(octadecanoylamino)ethyl]octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(=O)NCCNC(=O)CCCCCCCCCCCCCCCCC RKISUIUJZGSLEV-UHFFFAOYSA-N 0.000 claims description 3
DJWFNQUDPJTSAD-UHFFFAOYSA-N n-octadecyloctadecanamide Chemical compound CCCCCCCCCCCCCCCCCCNC(=O)CCCCCCCCCCCCCCCCC DJWFNQUDPJTSAD-UHFFFAOYSA-N 0.000 claims description 3
NKBWPOSQERPBFI-UHFFFAOYSA-N octadecyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CCCCCCCCCCCCCCCCC NKBWPOSQERPBFI-UHFFFAOYSA-N 0.000 claims description 3
239000003784 tall oil Substances 0.000 claims description 3
XBTRYWRVOBZSGM-UHFFFAOYSA-N (4-methylphenyl)methanediamine Chemical compound CC1=CC=C(C(N)N)C=C1 XBTRYWRVOBZSGM-UHFFFAOYSA-N 0.000 claims description 2
VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 claims description 2
PAOXFRSJRCGJLV-UHFFFAOYSA-N 2-[4-(2-aminoethyl)piperazin-1-yl]ethanamine Chemical compound NCCN1CCN(CCN)CC1 PAOXFRSJRCGJLV-UHFFFAOYSA-N 0.000 claims description 2
101100037762 Caenorhabditis elegans rnh-2 gene Proteins 0.000 claims description 2
235000021355 Stearic acid Nutrition 0.000 claims description 2
UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 claims description 2
XZAHJRZBUWYCBM-UHFFFAOYSA-N [1-(aminomethyl)cyclohexyl]methanamine Chemical compound NCC1(CN)CCCCC1 XZAHJRZBUWYCBM-UHFFFAOYSA-N 0.000 claims description 2
GKXVJHDEWHKBFH-UHFFFAOYSA-N [2-(aminomethyl)phenyl]methanamine Chemical compound NCC1=CC=CC=C1CN GKXVJHDEWHKBFH-UHFFFAOYSA-N 0.000 claims description 2
IMUDHTPIFIBORV-UHFFFAOYSA-N aminoethylpiperazine Chemical compound NCCN1CCNCC1 IMUDHTPIFIBORV-UHFFFAOYSA-N 0.000 claims description 2
GHWVXCQZPNWFRO-UHFFFAOYSA-N butane-2,3-diamine Chemical compound CC(N)C(C)N GHWVXCQZPNWFRO-UHFFFAOYSA-N 0.000 claims description 2
KNXOGJAYBBVCNF-UHFFFAOYSA-N decane-2,2-diamine Chemical compound CCCCCCCCC(C)(N)N KNXOGJAYBBVCNF-UHFFFAOYSA-N 0.000 claims description 2
QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 claims description 2
OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 claims description 2
GPCKFIWBUTWTDH-UHFFFAOYSA-N pentane-3,3-diamine Chemical compound CCC(N)(N)CC GPCKFIWBUTWTDH-UHFFFAOYSA-N 0.000 claims description 2
ZNZJJSYHZBXQSM-UHFFFAOYSA-N propane-2,2-diamine Chemical group CC(C)(N)N ZNZJJSYHZBXQSM-UHFFFAOYSA-N 0.000 claims description 2
239000008117 stearic acid Substances 0.000 claims description 2
FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 claims description 2
WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 claims 4
TVIDDXQYHWJXFK-UHFFFAOYSA-N dodecanedioic acid Chemical compound OC(=O)CCCCCCCCCCC(O)=O TVIDDXQYHWJXFK-UHFFFAOYSA-N 0.000 claims 4
238000002844 melting Methods 0.000 claims 4
230000008018 melting Effects 0.000 claims 4
CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 claims 4
MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 claims 2
TYFQFVWCELRYAO-UHFFFAOYSA-N suberic acid Chemical compound OC(=O)CCCCCCC(O)=O TYFQFVWCELRYAO-UHFFFAOYSA-N 0.000 claims 2
HFVMEOPYDLEHBR-UHFFFAOYSA-N (2-fluorophenyl)-phenylmethanol Chemical compound C=1C=CC=C(F)C=1C(O)C1=CC=CC=C1 HFVMEOPYDLEHBR-UHFFFAOYSA-N 0.000 claims 1
WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 claims 1
LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 claims 1
QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 claims 1
239000005642 Oleic acid Substances 0.000 claims 1
ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 claims 1
KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 claims 1
125000003916 ethylene diamine group Chemical group 0.000 claims 1
QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 claims 1
ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 claims 1
239000004952 Polyamide Substances 0.000 description 87
229920002647 polyamide Polymers 0.000 description 84
239000000853 adhesive Substances 0.000 description 28
230000001070 adhesive effect Effects 0.000 description 28
229920001187 thermosetting polymer Polymers 0.000 description 22
239000002184 metal Substances 0.000 description 18
239000000758 substrate Substances 0.000 description 14
238000009864 tensile test Methods 0.000 description 13
229920002554 vinyl polymer Polymers 0.000 description 9
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
229920005989 resin Polymers 0.000 description 8
239000011347 resin Substances 0.000 description 8
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 8
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 7
239000012943 hotmelt Substances 0.000 description 7
229920000642 polymer Polymers 0.000 description 7
238000006243 chemical reaction Methods 0.000 description 6
150000007513 acids Chemical class 0.000 description 5
238000009472 formulation Methods 0.000 description 5
238000006116 polymerization reaction Methods 0.000 description 5
239000000047 product Substances 0.000 description 5
239000000523 sample Substances 0.000 description 5
239000000126 substance Substances 0.000 description 5
IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 4
239000003795 chemical substances by application Substances 0.000 description 4
230000000052 comparative effect Effects 0.000 description 4
150000001991 dicarboxylic acids Chemical class 0.000 description 4
239000000463 material Substances 0.000 description 4
239000004417 polycarbonate Substances 0.000 description 4
229920000515 polycarbonate Polymers 0.000 description 4
238000003860 storage Methods 0.000 description 4
235000021122 unsaturated fatty acids Nutrition 0.000 description 4
150000004670 unsaturated fatty acids Chemical class 0.000 description 4
235000008331 Pinus X rigitaeda Nutrition 0.000 description 3
235000011613 Pinus brutia Nutrition 0.000 description 3
241000018646 Pinus brutia Species 0.000 description 3
238000009835 boiling Methods 0.000 description 3
-1 dipiperazine Chemical compound 0.000 description 3
150000002118 epoxides Chemical class 0.000 description 3
239000007788 liquid Substances 0.000 description 3
238000005259 measurement Methods 0.000 description 3
230000000704 physical effect Effects 0.000 description 3
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
241000202240 Morone americana Species 0.000 description 2
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 2
125000001931 aliphatic group Chemical group 0.000 description 2
239000003963 antioxidant agent Substances 0.000 description 2
239000003054 catalyst Substances 0.000 description 2
238000000576 coating method Methods 0.000 description 2
229920006332 epoxy adhesive Polymers 0.000 description 2
239000000178 monomer Substances 0.000 description 2
230000002028 premature Effects 0.000 description 2
238000012360 testing method Methods 0.000 description 2
229920006345 thermoplastic polyamide Polymers 0.000 description 2
239000013638 trimer Substances 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 1
NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
ZRYCRPNCXLQHPN-UHFFFAOYSA-N 3-hydroxy-2-methylbenzaldehyde Chemical compound CC1=C(O)C=CC=C1C=O ZRYCRPNCXLQHPN-UHFFFAOYSA-N 0.000 description 1
239000004135 Bone phosphate Substances 0.000 description 1
241000984642 Cura Species 0.000 description 1
239000009261 D 400 Substances 0.000 description 1
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
239000005977 Ethylene Substances 0.000 description 1
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
RVGRUAULSDPKGF-UHFFFAOYSA-N Poloxamer Chemical compound C1CO1.CC1CO1 RVGRUAULSDPKGF-UHFFFAOYSA-N 0.000 description 1
239000004793 Polystyrene Substances 0.000 description 1
230000009471 action Effects 0.000 description 1
238000012644 addition polymerization Methods 0.000 description 1
239000000654 additive Substances 0.000 description 1
239000012790 adhesive layer Substances 0.000 description 1
150000001336 alkenes Chemical class 0.000 description 1
229910000147 aluminium phosphate Inorganic materials 0.000 description 1
230000008859 change Effects 0.000 description 1
239000011248 coating agent Substances 0.000 description 1
239000003086 colorant Substances 0.000 description 1
239000007859 condensation product Substances 0.000 description 1
239000013068 control sample Substances 0.000 description 1
238000001816 cooling Methods 0.000 description 1
239000007822 coupling agent Substances 0.000 description 1
238000005336 cracking Methods 0.000 description 1
230000001419 dependent effect Effects 0.000 description 1
GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 1
238000004821 distillation Methods 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
239000010685 fatty oil Substances 0.000 description 1
239000000945 filler Substances 0.000 description 1
SLGWESQGEUXWJQ-UHFFFAOYSA-N formaldehyde;phenol Chemical compound O=C.OC1=CC=CC=C1 SLGWESQGEUXWJQ-UHFFFAOYSA-N 0.000 description 1
238000005194 fractionation Methods 0.000 description 1
239000003205 fragrance Substances 0.000 description 1
238000001879 gelation Methods 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
239000010410 layer Substances 0.000 description 1
239000000314 lubricant Substances 0.000 description 1
150000002691 malonic acids Chemical class 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
235000021313 oleic acid Nutrition 0.000 description 1
150000002889 oleic acids Chemical class 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
150000002913 oxalic acids Chemical class 0.000 description 1
229920001568 phenolic resin Polymers 0.000 description 1
239000004033 plastic Substances 0.000 description 1
229920003023 plastic Polymers 0.000 description 1
239000004014 plasticizer Substances 0.000 description 1
229920002223 polystyrene Polymers 0.000 description 1
150000003141 primary amines Chemical class 0.000 description 1
230000009467 reduction Effects 0.000 description 1
239000012744 reinforcing agent Substances 0.000 description 1
150000003335 secondary amines Chemical class 0.000 description 1
238000002791 soaking Methods 0.000 description 1
238000007711 solidification Methods 0.000 description 1
230000008023 solidification Effects 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
239000007858 starting material Substances 0.000 description 1
150000003442 suberic acids Chemical class 0.000 description 1
150000003444 succinic acids Chemical class 0.000 description 1
ORGHESHFQPYLAO-UHFFFAOYSA-N vinyl radical Chemical class C=[CH] ORGHESHFQPYLAO-UHFFFAOYSA-N 0.000 description 1
239000002023 wood Substances 0.000 description 1

Landscapes

Adhesives Or Adhesive Processes (AREA)
Epoxy Resins (AREA)
Compositions Of Macromolecular Compounds (AREA)

CA 2065185 1990-10-30 1992-04-06 Compositions reticulables a base de resines, utiles comme adhesifs thermofusibles Abandoned CA2065185A1 (fr)

Applications Claiming Priority (4)

Application Number	Priority Date	Filing Date	Title
US60679390A	1990-10-30	1990-10-30
US07/743,050		1991-08-09
US07/743,050 US5296556A (en)	1990-10-30	1991-08-09	Three-component curable resin compositions
US07/606,793		1991-08-09

Publications (1)

Publication Number	Publication Date
CA2065185A1 true CA2065185A1 (fr)	1993-02-10

Family

ID=27085332

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA 2065185 Abandoned CA2065185A1 (fr)	1990-10-30	1992-04-06	Compositions reticulables a base de resines, utiles comme adhesifs thermofusibles

Country Status (1)

Country	Link
CA (1)	CA2065185A1 (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CN113637156A (zh) *	2020-04-27	2021-11-12	财团法人纺织产业综合研究所	改质聚酰胺、其制作方法及单组分纤维

1992
- 1992-04-06 CA CA 2065185 patent/CA2065185A1/fr not_active Abandoned

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CN113637156A (zh) *	2020-04-27	2021-11-12	财团法人纺织产业综合研究所	改质聚酰胺、其制作方法及单组分纤维
CN113637156B (zh) *	2020-04-27	2024-04-12	财团法人纺织产业综合研究所	单组分纤维及其制作方法

Legal Events

Date	Code	Title	Description
1993-05-01	EEER	Examination request
2000-04-06	FZDE	Dead

Publication	Publication Date	Title
US5296556A (en)	1994-03-22	Three-component curable resin compositions
EP0442700B1 (fr)	1996-01-03	Compositions de résine thermofusibles durcissables à deux composants
US5612448A (en)	1997-03-18	Curable adhesive compositions containing polyamide resins
US4611051A (en)	1986-09-09	Novel poly(ester-amide) hot-melt adhesives
US3637550A (en)	1972-01-25	Silanated polyamide adhesive and its preparation
US4853460A (en)	1989-08-01	Long open assembly time vinyl-bonding polyamide from dimer acid
EP0441545A1 (fr)	1991-08-14	Compositions de résine à 2 composants thermofusible et réticulable
WO1999066003A1 (fr)	1999-12-23	Adhesif a chaud a base de polyamides et a temps d'assemblage ouvert long
WO2000037538A1 (fr)	2000-06-29	Adhesifs thermofusibles a base de polyamides
US5296557A (en)	1994-03-22	Two-component curable hot melt compositions
US20100282411A1 (en)	2010-11-11	Polyamides
US5424371A (en)	1995-06-13	Adhesive of amine-terminated, piperazine-containing polyamide and epoxy resin
US8119251B2 (en)	2012-02-21	Polyamides
EP0156949B1 (fr)	1991-01-02	Adhésifs fusibles à chaud à base de polyesteramide
US3397816A (en)	1968-08-20	Can having seams adhesively bonded by the reaction product of alkylene diamine, alkanol amine, dicarboxylic acid, and polymeric fat acid
US4882414A (en)	1989-11-21	Polyamide from polymeric fatty acid and long chain dicarboxylic acid
NO155391B (no)	1986-12-15	Polyesteramider og deres anvendelse ved klebing av organiske eller uorganiske substrater og stoepemasse samt blandinger inneholdende polyesteramidene.
US4191669A (en)	1980-03-04	Polyamides
JP3259182B2 (ja)	2002-02-25	ポリアミド及びポリエステルアミド、その製造方法、有機又は無機支持体の接着方法及び封止用コンパウンド