JPH0321577B2 - - Google Patents
Info
- Publication number
- JPH0321577B2 JPH0321577B2 JP22762986A JP22762986A JPH0321577B2 JP H0321577 B2 JPH0321577 B2 JP H0321577B2 JP 22762986 A JP22762986 A JP 22762986A JP 22762986 A JP22762986 A JP 22762986A JP H0321577 B2 JPH0321577 B2 JP H0321577B2
- Authority
- JP
- Japan
- Prior art keywords
- group
- groups
- compound
- component
- formula
- 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
- 239000000203 mixture Substances 0.000 claims description 19
- 125000003396 thiol group Chemical group [H]S* 0.000 claims description 17
- 229920000570 polyether Polymers 0.000 claims description 13
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 12
- 125000003700 epoxy group Chemical group 0.000 claims description 9
- 150000001875 compounds Chemical class 0.000 claims description 7
- 125000001183 hydrocarbyl group Chemical group 0.000 claims description 6
- 150000001491 aromatic compounds Chemical class 0.000 claims description 5
- 125000004432 carbon atom Chemical group C* 0.000 claims description 5
- 150000002391 heterocyclic compounds Chemical class 0.000 claims description 5
- 150000003961 organosilicon compounds Chemical class 0.000 claims description 5
- 125000003808 silyl group Chemical group [H][Si]([H])([H])[*] 0.000 claims description 4
- 239000003054 catalyst Substances 0.000 claims description 3
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 claims description 3
- JRNVQLOKVMWBFR-UHFFFAOYSA-N 1,2-benzenedithiol Chemical compound SC1=CC=CC=C1S JRNVQLOKVMWBFR-UHFFFAOYSA-N 0.000 claims description 2
- KKLFFMXJIHZXER-UHFFFAOYSA-N 3,4-dimethylbenzene-1,2-dithiol Chemical group CC1=CC=C(S)C(S)=C1C KKLFFMXJIHZXER-UHFFFAOYSA-N 0.000 claims description 2
- 125000003118 aryl group Chemical group 0.000 claims description 2
- 125000000623 heterocyclic group Chemical group 0.000 claims description 2
- 239000011256 inorganic filler Substances 0.000 claims description 2
- 229910003475 inorganic filler Inorganic materials 0.000 claims description 2
- KYAHXDQYSVFOOV-UHFFFAOYSA-N naphthalene-1,2-dithiol Chemical compound C1=CC=CC2=C(S)C(S)=CC=C21 KYAHXDQYSVFOOV-UHFFFAOYSA-N 0.000 claims description 2
- UKQMUPLYHOXQQR-UHFFFAOYSA-N phenylmethanedithiol Chemical compound SC(S)C1=CC=CC=C1 UKQMUPLYHOXQQR-UHFFFAOYSA-N 0.000 claims description 2
- 229910052710 silicon Inorganic materials 0.000 claims description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical group N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 2
- VLLMWSRANPNYQX-UHFFFAOYSA-N thiadiazole Chemical compound C1=CSN=N1.C1=CSN=N1 VLLMWSRANPNYQX-UHFFFAOYSA-N 0.000 claims 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 229910052757 nitrogen Inorganic materials 0.000 claims 1
- 229910052760 oxygen Inorganic materials 0.000 claims 1
- 239000001301 oxygen Substances 0.000 claims 1
- 125000004430 oxygen atom Chemical group O* 0.000 claims 1
- 125000004434 sulfur atom Chemical group 0.000 claims 1
- 238000010438 heat treatment Methods 0.000 description 31
- 238000003756 stirring Methods 0.000 description 30
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 24
- -1 Oxypropylene units Chemical group 0.000 description 23
- 230000015572 biosynthetic process Effects 0.000 description 13
- 238000003786 synthesis reaction Methods 0.000 description 13
- 229920001451 polypropylene glycol Polymers 0.000 description 12
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 10
- 229910000077 silane Inorganic materials 0.000 description 10
- 238000006116 polymerization reaction Methods 0.000 description 7
- 239000007788 liquid Substances 0.000 description 6
- 229920000642 polymer Polymers 0.000 description 6
- 239000004593 Epoxy Substances 0.000 description 5
- 230000001070 adhesive effect Effects 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 5
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 5
- 230000005484 gravity Effects 0.000 description 5
- 239000012299 nitrogen atmosphere Substances 0.000 description 5
- BIGYLAKFCGVRAN-UHFFFAOYSA-N 1,3,4-thiadiazolidine-2,5-dithione Chemical compound S=C1NNC(=S)S1 BIGYLAKFCGVRAN-UHFFFAOYSA-N 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 239000000047 product Substances 0.000 description 3
- 239000002994 raw material Substances 0.000 description 3
- 239000000565 sealant Substances 0.000 description 3
- 238000009864 tensile test Methods 0.000 description 3
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- WHGNXNCOTZPEEK-UHFFFAOYSA-N dimethoxy-methyl-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CO[Si](C)(OC)CCCOCC1CO1 WHGNXNCOTZPEEK-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 239000001023 inorganic pigment Substances 0.000 description 2
- 229910052740 iodine Inorganic materials 0.000 description 2
- 239000011630 iodine Substances 0.000 description 2
- 125000005702 oxyalkylene group Chemical group 0.000 description 2
- 125000006353 oxyethylene group Chemical group 0.000 description 2
- 239000013008 thixotropic agent Substances 0.000 description 2
- 150000003606 tin compounds Chemical class 0.000 description 2
- HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 description 1
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 230000006750 UV protection Effects 0.000 description 1
- 230000001464 adherent effect Effects 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- WYLQRHZSKIDFEP-UHFFFAOYSA-N benzene-1,4-dithiol Chemical compound SC1=CC=C(S)C=C1 WYLQRHZSKIDFEP-UHFFFAOYSA-N 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 125000004956 cyclohexylene group Chemical group 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- YQGOWXYZDLJBFL-UHFFFAOYSA-N dimethoxysilane Chemical compound CO[SiH2]OC YQGOWXYZDLJBFL-UHFFFAOYSA-N 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- AAPAGLBSROJFGM-UHFFFAOYSA-N naphthalene-1,5-dithiol Chemical compound C1=CC=C2C(S)=CC=CC2=C1S AAPAGLBSROJFGM-UHFFFAOYSA-N 0.000 description 1
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 239000003566 sealing material Substances 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 125000005371 silicon functional group Chemical group 0.000 description 1
- AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 description 1
- 235000019345 sodium thiosulphate Nutrition 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- CZDYPVPMEAXLPK-UHFFFAOYSA-N tetramethylsilane Chemical compound C[Si](C)(C)C CZDYPVPMEAXLPK-UHFFFAOYSA-N 0.000 description 1
- JXUKBNICSRJFAP-UHFFFAOYSA-N triethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CCO[Si](OCC)(OCC)CCCOCC1CO1 JXUKBNICSRJFAP-UHFFFAOYSA-N 0.000 description 1
- 125000003258 trimethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])[*:1] 0.000 description 1
Landscapes
- Sealing Material Composition (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Polyethers (AREA)
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61227629A JPS6383160A (ja) | 1986-09-26 | 1986-09-26 | 室温硬化性組成物 |
KR1019870009013A KR910000425B1 (ko) | 1986-09-26 | 1987-08-18 | 폴리에테르 및 그 제조방법 |
KR1019900012512A KR920000927B1 (ko) | 1986-09-26 | 1990-08-13 | 폴리에테르를 이용한 실온 경화성 조성물 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61227629A JPS6383160A (ja) | 1986-09-26 | 1986-09-26 | 室温硬化性組成物 |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS6383160A JPS6383160A (ja) | 1988-04-13 |
JPH0321577B2 true JPH0321577B2 (ko) | 1991-03-25 |
Family
ID=16863907
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP61227629A Granted JPS6383160A (ja) | 1986-09-26 | 1986-09-26 | 室温硬化性組成物 |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6383160A (ko) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3816808C1 (ko) * | 1988-05-14 | 1989-10-26 | Teroson Gmbh, 6900 Heidelberg, De | |
JPWO2004074330A1 (ja) | 2003-02-18 | 2006-06-01 | コニシ株式会社 | 硬化性樹脂、その製造方法及び硬化性樹脂組成物 |
-
1986
- 1986-09-26 JP JP61227629A patent/JPS6383160A/ja active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS6383160A (ja) | 1988-04-13 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JPH032450B2 (ko) | ||
US4786667A (en) | Polyether end-blocked with hydrolyzable silyl groups, method of manufacturing and room temperature curable composition using the polyether | |
JP2718962B2 (ja) | 加水分解性シリル基で分子鎖末端が閉塞されたポリブタジエン、その製造方法およびそれを含有する室温硬化性組成物 | |
EP0341322B1 (en) | Polyether end-blocked with hydrolyzable silyl groups, method of manufacturing and room temperature curable composition using the polyether | |
US4950707A (en) | Polyether end-blocked with hydrolyzable silyl groups, method of manufacturing and room temperature curable composition using the polyether | |
US4847357A (en) | Polyether end-blocked with hydrolyzable silyl groups, method of manufacturing and room temperature curable composition thereof | |
JPH0321577B2 (ko) | ||
EP0621316A1 (en) | Organic silicon compounds and curable organopolysiloxane compositions | |
JPH01292061A (ja) | 室温硬化性組成物 | |
JPH0313261B2 (ko) | ||
JP2688499B2 (ja) | 加水分解性シリル基で分子鎖末端が閉塞されたポリエーテル、その製造方法およびそれを含有する室温硬化性組成物 | |
JPH0257824B2 (ko) | ||
KR920000927B1 (ko) | 폴리에테르를 이용한 실온 경화성 조성물 | |
JPH0714998B2 (ja) | 加水分解性シリル基で分子鎖末端が閉塞されたポリエ−テル | |
JPH0257823B2 (ko) | ||
JPH0257822B2 (ko) | ||
JPH0477516A (ja) | 硬化性組成物 | |
JPH0457695B2 (ko) | ||
JP3012876B2 (ja) | 加水分解性シリル基で分子鎖末端が閉塞された重合体、その製造方法およびそれを含有する室温硬化性組成物 | |
JPS62181321A (ja) | 室温硬化性組成物 | |
JPH086024B2 (ja) | 室温硬化性組成物 | |
JPS62181320A (ja) | 加水分解性シリル基で末端が閉塞された共重合体 | |
JPH0477525A (ja) | ポリエーテル共重合体、その製造方法およびそれを含有する組成物 | |
JPS6333425A (ja) | 加水分解性シリル基で分子鎖末端が閉塞された共重合体およびその製造方法 | |
JPH0477551A (ja) | 室温硬化性組成物 |