JPS6147773A - 繊維用接着剤 - Google Patents

繊維用接着剤

Info

Publication number: JPS6147773A
Authority: JP; Japan
Prior art keywords: adhesive; cloth; group; softening point; parts
Prior art date: 1984-08-14
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.): Granted

Application number

JP16884684A

Other languages

English (en)

Japanese (ja)

Other versions

JPH0149392B2 (2

Inventor

Masayuki Mishima

雅之三島

Yuichi Ueda

雄一上田

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.)

National Institute of Advanced Industrial Science and Technology AIST

Original Assignee

Agency of Industrial Science and Technology

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1984-08-14

Filing date

1984-08-14

Publication date

1986-03-08

1984-08-14 Application filed by Agency of Industrial Science and Technology filed Critical Agency of Industrial Science and Technology

1984-08-14 Priority to JP16884684A priority Critical patent/JPS6147773A/ja

1986-03-08 Publication of JPS6147773A publication Critical patent/JPS6147773A/ja

1989-10-24 Publication of JPH0149392B2 publication Critical patent/JPH0149392B2/ja

Status Granted legal-status Critical Current

Links

239000000853 adhesive Substances 0.000 title claims abstract description 32
230000001070 adhesive effect Effects 0.000 title claims abstract description 32
239000004744 fabric Substances 0.000 title claims abstract description 26
229920000642 polymer Polymers 0.000 claims abstract description 42
229910052757 nitrogen Inorganic materials 0.000 claims abstract description 14
229910052760 oxygen Inorganic materials 0.000 claims abstract description 10
239000002131 composite material Substances 0.000 claims abstract description 9
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 9
125000003545 alkoxy group Chemical group 0.000 claims abstract description 4
125000000962 organic group Chemical group 0.000 claims abstract description 4
238000009833 condensation Methods 0.000 claims description 29
230000005494 condensation Effects 0.000 claims description 29
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 25
125000004432 carbon atom Chemical group C* 0.000 claims description 14
239000000835 fiber Substances 0.000 claims description 13
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 7
239000001257 hydrogen Substances 0.000 claims description 7
239000001301 oxygen Substances 0.000 claims description 7
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 3
239000011593 sulfur Substances 0.000 claims description 3
229910052717 sulfur Inorganic materials 0.000 claims description 3
XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 2
229910052710 silicon Inorganic materials 0.000 claims description 2
239000010703 silicon Substances 0.000 claims description 2
125000001183 hydrocarbyl group Chemical group 0.000 claims 2
150000002431 hydrogen Chemical class 0.000 claims 1
239000000126 substance Substances 0.000 claims 1
-1 organosilane compound Chemical class 0.000 abstract description 21
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 12
238000005108 dry cleaning Methods 0.000 abstract description 11
238000005406 washing Methods 0.000 abstract description 11
125000003277 amino group Chemical group 0.000 abstract description 6
230000015572 biosynthetic process Effects 0.000 abstract description 4
150000002430 hydrocarbons Chemical class 0.000 abstract description 4
239000004215 Carbon black (E152) Substances 0.000 abstract description 3
229930195733 hydrocarbon Natural products 0.000 abstract description 3
238000010409 ironing Methods 0.000 abstract description 3
230000001588 bifunctional effect Effects 0.000 abstract 1
239000002253 acid Substances 0.000 description 19
238000012360 testing method Methods 0.000 description 10
229920005989 resin Polymers 0.000 description 9
239000011347 resin Substances 0.000 description 9
239000002904 solvent Substances 0.000 description 8
150000007513 acids Chemical class 0.000 description 7
238000006243 chemical reaction Methods 0.000 description 7
229920006305 unsaturated polyester Polymers 0.000 description 7
QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 6
WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 6
239000004831 Hot glue Substances 0.000 description 5
150000002009 diols Chemical class 0.000 description 5
239000012943 hotmelt Substances 0.000 description 5
125000002887 hydroxy group Chemical group [H]O* 0.000 description 5
238000000034 method Methods 0.000 description 5
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical group OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 4
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 4
WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 4
WOZVHXUHUFLZGK-UHFFFAOYSA-N dimethyl terephthalate Chemical compound COC(=O)C1=CC=C(C(=O)OC)C=C1 WOZVHXUHUFLZGK-UHFFFAOYSA-N 0.000 description 4
LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 4
125000004435 hydrogen atom Chemical class [H]* 0.000 description 4
229920000728 polyester Polymers 0.000 description 4
229920001451 polypropylene glycol Polymers 0.000 description 4
125000003808 silyl group Chemical group [H][Si]([H])([H])[*] 0.000 description 4
229920001169 thermoplastic Polymers 0.000 description 4
239000004416 thermosoftening plastic Substances 0.000 description 4
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
238000005481 NMR spectroscopy Methods 0.000 description 3
239000004952 Polyamide Substances 0.000 description 3
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
125000005370 alkoxysilyl group Chemical group 0.000 description 3
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
125000005442 diisocyanate group Chemical group 0.000 description 3
230000032050 esterification Effects 0.000 description 3
238000005886 esterification reaction Methods 0.000 description 3
150000002148 esters Chemical class 0.000 description 3
239000000463 material Substances 0.000 description 3
229920006149 polyester-amide block copolymer Polymers 0.000 description 3
239000000243 solution Substances 0.000 description 3
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 3
WYTZZXDRDKSJID-UHFFFAOYSA-N (3-aminopropyl)triethoxysilane Chemical compound CCO[Si](OCC)(OCC)CCCN WYTZZXDRDKSJID-UHFFFAOYSA-N 0.000 description 2
229920000742 Cotton Polymers 0.000 description 2
PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 2
ZHNUHDYFZUAESO-UHFFFAOYSA-N Formamide Chemical compound NC=O ZHNUHDYFZUAESO-UHFFFAOYSA-N 0.000 description 2
YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical compound C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 2
ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Chemical group OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
238000010521 absorption reaction Methods 0.000 description 2
239000001361 adipic acid Substances 0.000 description 2
235000011037 adipic acid Nutrition 0.000 description 2
125000000217 alkyl group Chemical group 0.000 description 2
125000002947 alkylene group Chemical group 0.000 description 2
125000003118 aryl group Chemical group 0.000 description 2
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
150000004985 diamines Chemical class 0.000 description 2
125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 2
230000000694 effects Effects 0.000 description 2
239000001530 fumaric acid Substances 0.000 description 2
ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 description 2
NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 2
229910052742 iron Inorganic materials 0.000 description 2
QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
239000002648 laminated material Substances 0.000 description 2
229940049920 malate Drugs 0.000 description 2
229920002647 polyamide Polymers 0.000 description 2
238000006116 polymerization reaction Methods 0.000 description 2
238000012545 processing Methods 0.000 description 2
YPFDHNVEDLHUCE-UHFFFAOYSA-N propane-1,3-diol Chemical compound OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 2
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
239000000376 reactant Substances 0.000 description 2
238000010992 reflux Methods 0.000 description 2
238000003756 stirring Methods 0.000 description 2
239000004753 textile Substances 0.000 description 2
238000005809 transesterification reaction Methods 0.000 description 2
JOYRKODLDBILNP-UHFFFAOYSA-N urethane group Chemical group NC(=O)OCC JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 2
ZXHZWRZAWJVPIC-UHFFFAOYSA-N 1,2-diisocyanatonaphthalene Chemical compound C1=CC=CC2=C(N=C=O)C(N=C=O)=CC=C21 ZXHZWRZAWJVPIC-UHFFFAOYSA-N 0.000 description 1
AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 description 1
WTPYFJNYAMXZJG-UHFFFAOYSA-N 2-[4-(2-hydroxyethoxy)phenoxy]ethanol Chemical compound OCCOC1=CC=C(OCCO)C=C1 WTPYFJNYAMXZJG-UHFFFAOYSA-N 0.000 description 1
GLISOBUNKGBQCL-UHFFFAOYSA-N 3-[ethoxy(dimethyl)silyl]propan-1-amine Chemical compound CCO[Si](C)(C)CCCN GLISOBUNKGBQCL-UHFFFAOYSA-N 0.000 description 1
SJECZPVISLOESU-UHFFFAOYSA-N 3-trimethoxysilylpropan-1-amine Chemical compound CO[Si](OC)(OC)CCCN SJECZPVISLOESU-UHFFFAOYSA-N 0.000 description 1
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 1
DZIHTWJGPDVSGE-UHFFFAOYSA-N 4-[(4-aminocyclohexyl)methyl]cyclohexan-1-amine Chemical compound C1CC(N)CCC1CC1CCC(N)CC1 DZIHTWJGPDVSGE-UHFFFAOYSA-N 0.000 description 1
238000012935 Averaging Methods 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical group N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 description 1
UDSFAEKRVUSQDD-UHFFFAOYSA-N Dimethyl adipate Chemical compound COC(=O)CCCCC(=O)OC UDSFAEKRVUSQDD-UHFFFAOYSA-N 0.000 description 1
239000004593 Epoxy Substances 0.000 description 1
YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 description 1
239000005057 Hexamethylene diisocyanate Substances 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
CYTYCFOTNPOANT-UHFFFAOYSA-N Perchloroethylene Chemical group ClC(Cl)=C(Cl)Cl CYTYCFOTNPOANT-UHFFFAOYSA-N 0.000 description 1
229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
238000007259 addition reaction Methods 0.000 description 1
238000007605 air drying Methods 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
125000002723 alicyclic group Chemical group 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
150000008064 anhydrides Chemical class 0.000 description 1
239000003963 antioxidant agent Substances 0.000 description 1
230000003078 antioxidant effect Effects 0.000 description 1
125000004429 atom Chemical group 0.000 description 1
229960004217 benzyl alcohol Drugs 0.000 description 1
238000007664 blowing Methods 0.000 description 1
235000008429 bread Nutrition 0.000 description 1
YHWCPXVTRSHPNY-UHFFFAOYSA-N butan-1-olate;titanium(4+) Chemical compound [Ti+4].CCCC[O-].CCCC[O-].CCCC[O-].CCCC[O-] YHWCPXVTRSHPNY-UHFFFAOYSA-N 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 Chemical group 0.000 description 1
239000003054 catalyst Substances 0.000 description 1
150000001875 compounds Chemical class 0.000 description 1
238000001816 cooling Methods 0.000 description 1
PDXRQENMIVHKPI-UHFFFAOYSA-N cyclohexane-1,1-diol Chemical compound OC1(O)CCCCC1 PDXRQENMIVHKPI-UHFFFAOYSA-N 0.000 description 1
230000003247 decreasing effect Effects 0.000 description 1
230000018044 dehydration Effects 0.000 description 1
238000006297 dehydration reaction Methods 0.000 description 1
239000003599 detergent Substances 0.000 description 1
230000006866 deterioration Effects 0.000 description 1
238000011161 development Methods 0.000 description 1
IEPRKVQEAMIZSS-AATRIKPKSA-N diethyl fumarate Chemical compound CCOC(=O)\C=C\C(=O)OCC IEPRKVQEAMIZSS-AATRIKPKSA-N 0.000 description 1
239000000539 dimer Substances 0.000 description 1
VNGOYPQMJFJDLV-UHFFFAOYSA-N dimethyl benzene-1,3-dicarboxylate Chemical compound COC(=O)C1=CC=CC(C(=O)OC)=C1 VNGOYPQMJFJDLV-UHFFFAOYSA-N 0.000 description 1
229910001873 dinitrogen Inorganic materials 0.000 description 1
238000004821 distillation Methods 0.000 description 1
238000001035 drying Methods 0.000 description 1
238000005516 engineering process Methods 0.000 description 1
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
230000007062 hydrolysis Effects 0.000 description 1
238000006460 hydrolysis reaction Methods 0.000 description 1
239000012948 isocyanate Substances 0.000 description 1
150000002513 isocyanates Chemical class 0.000 description 1
230000014759 maintenance of location Effects 0.000 description 1
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical group OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
239000011976 maleic acid Chemical group 0.000 description 1
FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
BJEPYKJPYRNKOW-UHFFFAOYSA-N malic acid Chemical compound OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
239000000203 mixture Substances 0.000 description 1
230000004048 modification Effects 0.000 description 1
238000012986 modification Methods 0.000 description 1
125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
125000004433 nitrogen atom Chemical group N* 0.000 description 1
229920006122 polyamide resin Polymers 0.000 description 1
229920001225 polyester resin Polymers 0.000 description 1
229920005672 polyolefin resin Polymers 0.000 description 1
238000012805 post-processing Methods 0.000 description 1
239000000843 powder Substances 0.000 description 1
239000001294 propane Substances 0.000 description 1
210000004189 reticular formation Anatomy 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
FZHAPNGMFPVSLP-UHFFFAOYSA-N silanamine Chemical compound [SiH3]N FZHAPNGMFPVSLP-UHFFFAOYSA-N 0.000 description 1
229910000077 silane Inorganic materials 0.000 description 1
125000005372 silanol group Chemical group 0.000 description 1
150000003377 silicon compounds Chemical class 0.000 description 1
239000000344 soap Substances 0.000 description 1
239000011780 sodium chloride Substances 0.000 description 1
230000008961 swelling Effects 0.000 description 1
229950011008 tetrachloroethylene Drugs 0.000 description 1
229920005992 thermoplastic resin Polymers 0.000 description 1
229920001187 thermosetting polymer Polymers 0.000 description 1
239000004634 thermosetting polymer Substances 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
238000012546 transfer Methods 0.000 description 1
LFGUOQUMQLUOAM-UHFFFAOYSA-N tris(2-ethylhexoxy)silane Chemical compound CCCCC(CC)CO[SiH](OCC(CC)CCCC)OCC(CC)CCCC LFGUOQUMQLUOAM-UHFFFAOYSA-N 0.000 description 1

Landscapes

Polyesters Or Polycarbonates (AREA)
Adhesives Or Adhesive Processes (AREA)
Manufacturing Of Multi-Layer Textile Fabrics (AREA)

JP16884684A 1984-08-14 1984-08-14 繊維用接着剤 Granted JPS6147773A (ja)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
JP16884684A JPS6147773A (ja)	1984-08-14	1984-08-14	繊維用接着剤

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP16884684A JPS6147773A (ja)	1984-08-14	1984-08-14	繊維用接着剤

Publications (2)

Publication Number	Publication Date
JPS6147773A true JPS6147773A (ja)	1986-03-08
JPH0149392B2 JPH0149392B2 (2)	1989-10-24

Family

ID=15875618

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP16884684A Granted JPS6147773A (ja)	1984-08-14	1984-08-14	繊維用接着剤

Country Status (1)

Country	Link
JP (1)	JPS6147773A (2)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPH03227219A (ja) *	1990-02-01	1991-10-08	Paron:Kk	家具・パーティション構成体の接着方法
JP2017508818A (ja) *	2013-12-12	2017-03-30	ダウグローバルテクノロジーズエルエルシー	ウレタン系用のアミノシラン接着促進剤

1984
- 1984-08-14 JP JP16884684A patent/JPS6147773A/ja active Granted

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPH03227219A (ja) *	1990-02-01	1991-10-08	Paron:Kk	家具・パーティション構成体の接着方法
JP2017508818A (ja) *	2013-12-12	2017-03-30	ダウグローバルテクノロジーズエルエルシー	ウレタン系用のアミノシラン接着促進剤

Also Published As

Publication number	Publication date
JPH0149392B2 (2)	1989-10-24

Legal Events

Date	Code	Title	Description
2004-08-14	EXPY	Cancellation because of completion of term

Publication	Publication Date	Title
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JP3373652B2 (ja)	2003-02-04	紫外線吸収性ポリウレタンおよびポリエステル
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US2915480A (en)	1959-12-01	Aziridine-carboxylic acid polymers
US3967030A (en)	1976-06-29	Siloxanes
JPH07308995A (ja)	1995-11-28	発泡プラスチック製の防水・通気性雨着及び防水性製品
JPS61218631A (ja)	1986-09-29	架橋性ホットメルト接着剤の製造方法
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US3716517A (en)	1973-02-13	Siloxane polymers for soil-repellent and soil-release textile finishes
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US3007899A (en)	1961-11-07	Polyurethane (ester glycol) compositions
US4511727A (en)	1985-04-16	Quaternary ammonium-functional silicon compounds
JPS58206596A (ja)	1983-12-01	第四アンモニウム−珪素化合物
JPS6241989B2 (2)	1987-09-05
US3403046A (en)	1968-09-24	Method of forming a water vapor permeable film and coating on a substrate
JPS60252638A (ja)	1985-12-13	多孔性シ−ト材料の製造方法
US4299879A (en)	1981-11-10	Process for treating a textile material
US4867750A (en)	1989-09-19	Alkoxylated polyesters
US3642972A (en)	1972-02-15	Process of producing nonwoven fabrics using aziridine-modified polyurethane bonding agent
JPH0543792A (ja)	1993-02-23	ポリアミノ酸ウレタン樹脂及びそれを用いた製品
US4615706A (en)	1986-10-07	Quaternary ammonium-functional silicon compounds
JPS598429B2 (ja)	1984-02-24	帯電防止処理組成物
JPH02225581A (ja)	1990-09-07	ホットメルト接着剤
JPH04175369A (ja)	1992-06-23	合成樹脂組成物及びそれを用いた合成シート

JPS6147773A - 繊維用接着剤 - Google Patents

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