JPS6249287B2 - - Google Patents

Info

Publication number: JPS6249287B2
Authority: JP; Japan
Prior art keywords: moisture; composition; curable composition; diisocyanate; liquid diene
Prior art date: 1984-11-26
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

Application number

JP59248160A

Other languages

English (en)

Japanese (ja)

Other versions

JPS61126125A (ja

Inventor

Matsunori Yasuyoshi

Juzo Kurashige

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.)

Idemitsu Petrochemical Co Ltd

Original Assignee

Idemitsu Petrochemical Co Ltd

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.)

1984-11-26

Filing date

1984-11-26

Publication date

1987-10-19

1984-11-26 Application filed by Idemitsu Petrochemical Co Ltd filed Critical Idemitsu Petrochemical Co Ltd

1984-11-26 Priority to JP59248160A priority Critical patent/JPS61126125A/ja

1986-06-13 Publication of JPS61126125A publication Critical patent/JPS61126125A/ja

1987-10-19 Publication of JPS6249287B2 publication Critical patent/JPS6249287B2/ja

Status Granted legal-status Critical Current

Links

239000000203 mixture Substances 0.000 claims description 37
150000001993 dienes Chemical class 0.000 claims description 19
239000007788 liquid Substances 0.000 claims description 18
229920000642 polymer Polymers 0.000 claims description 17
239000012948 isocyanate Substances 0.000 claims description 16
-1 isocyanate compound Chemical class 0.000 claims description 16
238000000034 method Methods 0.000 claims description 16
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 13
150000001875 compounds Chemical class 0.000 claims description 7
239000005056 polyisocyanate Substances 0.000 claims description 6
229920001228 polyisocyanate Polymers 0.000 claims description 6
239000000126 substance Substances 0.000 claims description 4
IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims description 3
239000010426 asphalt Substances 0.000 description 7
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 6
229920001577 copolymer Polymers 0.000 description 6
239000000047 product Substances 0.000 description 5
239000011248 coating agent Substances 0.000 description 4
238000000576 coating method Methods 0.000 description 4
239000000463 material Substances 0.000 description 4
239000000178 monomer Substances 0.000 description 4
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
239000000654 additive Substances 0.000 description 3
239000011247 coating layer Substances 0.000 description 3
230000000052 comparative effect Effects 0.000 description 3
238000004519 manufacturing process Methods 0.000 description 3
230000000704 physical effect Effects 0.000 description 3
238000003756 stirring Methods 0.000 description 3
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 3
PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
239000005057 Hexamethylene diisocyanate Substances 0.000 description 2
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
239000005058 Isophorone diisocyanate Substances 0.000 description 2
RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 2
ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 2
UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 2
238000007259 addition reaction Methods 0.000 description 2
TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
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 2
WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
125000004432 carbon atom Chemical group C* 0.000 description 2
239000003054 catalyst Substances 0.000 description 2
238000006243 chemical reaction Methods 0.000 description 2
239000007795 chemical reaction product Substances 0.000 description 2
RWGFKTVRMDUZSP-UHFFFAOYSA-N cumene Chemical compound CC(C)C1=CC=CC=C1 RWGFKTVRMDUZSP-UHFFFAOYSA-N 0.000 description 2
229910001873 dinitrogen Inorganic materials 0.000 description 2
230000000694 effects Effects 0.000 description 2
238000010438 heat treatment Methods 0.000 description 2
RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 2
NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 2
229910052751 metal Inorganic materials 0.000 description 2
239000002184 metal Substances 0.000 description 2
239000004014 plasticizer Substances 0.000 description 2
239000010734 process oil Substances 0.000 description 2
229920005989 resin Polymers 0.000 description 2
239000011347 resin Substances 0.000 description 2
150000003839 salts Chemical class 0.000 description 2
IMNIMPAHZVJRPE-UHFFFAOYSA-N triethylenediamine Chemical compound C1CN2CCN1CC2 IMNIMPAHZVJRPE-UHFFFAOYSA-N 0.000 description 2
239000008096 xylene Substances 0.000 description 2
FKTHNVSLHLHISI-UHFFFAOYSA-N 1,2-bis(isocyanatomethyl)benzene Chemical compound O=C=NCC1=CC=CC=C1CN=C=O FKTHNVSLHLHISI-UHFFFAOYSA-N 0.000 description 1
SBJCUZQNHOLYMD-UHFFFAOYSA-N 1,5-Naphthalene diisocyanate Chemical compound C1=CC=C2C(N=C=O)=CC=CC2=C1N=C=O SBJCUZQNHOLYMD-UHFFFAOYSA-N 0.000 description 1
DKJBREHOVWISMR-UHFFFAOYSA-N 1-chloro-2,3-diisocyanatobenzene Chemical compound ClC1=CC=CC(N=C=O)=C1N=C=O DKJBREHOVWISMR-UHFFFAOYSA-N 0.000 description 1
HNNQYHFROJDYHQ-UHFFFAOYSA-N 3-(4-ethylcyclohexyl)propanoic acid 3-(3-ethylcyclopentyl)propanoic acid Chemical compound CCC1CCC(CCC(O)=O)C1.CCC1CCC(CCC(O)=O)CC1 HNNQYHFROJDYHQ-UHFFFAOYSA-N 0.000 description 1
MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 1
JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
QORUGOXNWQUALA-UHFFFAOYSA-N N=C=O.N=C=O.N=C=O.C1=CC=C(C(C2=CC=CC=C2)C2=CC=CC=C2)C=C1 Chemical compound N=C=O.N=C=O.N=C=O.C1=CC=C(C(C2=CC=CC=C2)C2=CC=CC=C2)C=C1 QORUGOXNWQUALA-UHFFFAOYSA-N 0.000 description 1
229920000459 Nitrile rubber Polymers 0.000 description 1
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
229920000538 Poly[(phenyl isocyanate)-co-formaldehyde] Polymers 0.000 description 1
239000000853 adhesive Substances 0.000 description 1
230000001070 adhesive effect Effects 0.000 description 1
230000003712 anti-aging effect Effects 0.000 description 1
239000012298 atmosphere Substances 0.000 description 1
PASDCCFISLVPSO-UHFFFAOYSA-N benzoyl chloride Chemical compound ClC(=O)C1=CC=CC=C1 PASDCCFISLVPSO-UHFFFAOYSA-N 0.000 description 1
BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 1
NTXGQCSETZTARF-UHFFFAOYSA-N buta-1,3-diene;prop-2-enenitrile Chemical compound C=CC=C.C=CC#N NTXGQCSETZTARF-UHFFFAOYSA-N 0.000 description 1
229910000019 calcium carbonate Inorganic materials 0.000 description 1
239000006229 carbon black Substances 0.000 description 1
150000001735 carboxylic acids Chemical class 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
238000001816 cooling Methods 0.000 description 1
230000000875 corresponding effect Effects 0.000 description 1
MDRWOAQZCGCEQK-UHFFFAOYSA-N cyclohexane;1,2-diisocyanatobenzene Chemical compound C1CCCCC1.O=C=NC1=CC=CC=C1N=C=O MDRWOAQZCGCEQK-UHFFFAOYSA-N 0.000 description 1
239000012975 dibutyltin dilaurate Substances 0.000 description 1
229940105990 diglycerin Drugs 0.000 description 1
GPLRAVKSCUXZTP-UHFFFAOYSA-N diglycerol Chemical compound OCC(O)COCC(O)CO GPLRAVKSCUXZTP-UHFFFAOYSA-N 0.000 description 1
230000001747 exhibiting effect Effects 0.000 description 1
239000000945 filler Substances 0.000 description 1
125000000524 functional group Chemical group 0.000 description 1
235000011187 glycerol Nutrition 0.000 description 1
229920001519 homopolymer Polymers 0.000 description 1
150000002513 isocyanates Chemical class 0.000 description 1
FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
238000002156 mixing Methods 0.000 description 1
125000005474 octanoate group Chemical group 0.000 description 1
WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 1
239000012188 paraffin wax Substances 0.000 description 1
230000035515 penetration Effects 0.000 description 1
239000003208 petroleum Substances 0.000 description 1
150000003014 phosphoric acid esters Chemical class 0.000 description 1
XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical class OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 1
229920002587 poly(1,3-butadiene) polymer Polymers 0.000 description 1
229920001451 polypropylene glycol Polymers 0.000 description 1
239000002994 raw material Substances 0.000 description 1
239000012429 reaction media Substances 0.000 description 1
238000007789 sealing Methods 0.000 description 1
230000036558 skin tension Effects 0.000 description 1
239000002904 solvent Substances 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
150000003505 terpenes Chemical class 0.000 description 1
235000007586 terpenes Nutrition 0.000 description 1
150000003672 ureas Chemical class 0.000 description 1
238000004078 waterproofing Methods 0.000 description 1

Landscapes

Polyurethanes Or Polyureas (AREA)

JP59248160A 1984-11-26 1984-11-26 湿気硬化性組成物の貯蔵方法 Granted JPS61126125A (ja)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
JP59248160A JPS61126125A (ja)	1984-11-26	1984-11-26	湿気硬化性組成物の貯蔵方法

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP59248160A JPS61126125A (ja)	1984-11-26	1984-11-26	湿気硬化性組成物の貯蔵方法

Publications (2)

Publication Number	Publication Date
JPS61126125A JPS61126125A (ja)	1986-06-13
JPS6249287B2 true JPS6249287B2 (fr)	1987-10-19

Family

ID=17174111

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP59248160A Granted JPS61126125A (ja)	1984-11-26	1984-11-26	湿気硬化性組成物の貯蔵方法

Country Status (1)

Country	Link
JP (1)	JPS61126125A (fr)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CA2341202A1 (fr) *	1998-08-19	2000-03-02	Umarani Rajalingam	Compositions a reseau elastomere et polyurethane bitumineux enchevetres
US12157823B2 (en)	2018-12-18	2024-12-03	Basf Se	Asphalt composition comprising monomeric MDI as thermosetting reactive compound
CN111253111A (zh) *	2020-01-16	2020-06-09	交通运输部科学研究院	沥青路面常温快速修补材料的制备方法及使用方法

1984
- 1984-11-26 JP JP59248160A patent/JPS61126125A/ja active Granted

Also Published As

Publication number	Publication date
JPS61126125A (ja)	1986-06-13

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CA2267702C (fr)	2008-03-25	Groupes amines latents et groupes isocyanates comprenant des pre-polymeres polyurethanes, leurs modes de production et d'utilisation
JPS6045673B2 (ja)	1985-10-11	ポリウレタンシ−ラント
US4234714A (en)	1980-11-18	Preparation of single-phase, urethane prepolymers from hydroxy-terminated diene polymers
JP4621460B2 (ja)	2011-01-26	液状重合体組成物
JPH0255451B2 (fr)	1990-11-27
JPS6249287B2 (fr)	1987-10-19
JPS6247900B2 (fr)	1987-10-09
JPS6315294B2 (fr)	1988-04-04
JPS6248988B2 (fr)	1987-10-16
JPH0251950B2 (fr)	1990-11-09
JPH032887B2 (fr)	1991-01-17
JPH0355488B2 (fr)	1991-08-23
JPH0242368B2 (fr)	1990-09-21
JPH0361713B2 (fr)	1991-09-20
JPH0349936B2 (fr)	1991-07-31
JPH0130852B2 (fr)	1989-06-22
JPS60118782A (ja)	1985-06-26	耐熱性粘着組成物
JPH0313269B2 (fr)	1991-02-22
JPH0420605Y2 (fr)	1992-05-12
JPS61166873A (ja)	1986-07-28	防水シ−ト用接着剤
JPH0723421B2 (ja)	1995-03-15	ポリオレフィン系ポリイソシアネート組成物
JPS588705B2 (ja)	1983-02-17	粘着組成物
JPH0436351A (ja)	1992-02-06	二液性ポリウレタン組成物