JPS59152951A - ポリエステル型ブロツク共重合体組成物 - Google Patents
ポリエステル型ブロツク共重合体組成物Info
- Publication number
- JPS59152951A JPS59152951A JP2812683A JP2812683A JPS59152951A JP S59152951 A JPS59152951 A JP S59152951A JP 2812683 A JP2812683 A JP 2812683A JP 2812683 A JP2812683 A JP 2812683A JP S59152951 A JPS59152951 A JP S59152951A
- Authority
- JP
- Japan
- Prior art keywords
- block copolymer
- polyester
- type block
- epoxy compound
- heat
- 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.)
- Granted
Links
- 229920000728 polyester Polymers 0.000 title claims abstract description 35
- 229920001400 block copolymer Polymers 0.000 title claims abstract description 23
- 239000000203 mixture Substances 0.000 title claims abstract description 10
- 150000001875 compounds Chemical class 0.000 claims abstract description 24
- 239000004593 Epoxy Substances 0.000 claims abstract description 18
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical class C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 claims abstract description 13
- 125000003118 aryl group Chemical group 0.000 claims abstract description 11
- 150000002596 lactones Chemical class 0.000 claims abstract description 10
- 150000003464 sulfur compounds Chemical class 0.000 claims abstract description 4
- 150000002989 phenols Chemical class 0.000 claims abstract description 3
- 239000012760 heat stabilizer Substances 0.000 claims description 13
- -1 polyethylene terephthalate Polymers 0.000 abstract description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 7
- 238000006243 chemical reaction Methods 0.000 abstract description 5
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 abstract description 4
- 239000002253 acid Substances 0.000 abstract description 3
- PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-Caprolactone Chemical compound O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 0.000 abstract description 3
- 229920000139 polyethylene terephthalate Polymers 0.000 abstract description 2
- 239000005020 polyethylene terephthalate Substances 0.000 abstract description 2
- 238000002156 mixing Methods 0.000 description 12
- 238000004519 manufacturing process Methods 0.000 description 11
- 125000004432 carbon atom Chemical group C* 0.000 description 10
- 125000001183 hydrocarbyl group Chemical group 0.000 description 8
- BGYHLZZASRKEJE-UHFFFAOYSA-N [3-[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxy]-2,2-bis[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxymethyl]propyl] 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CCC(=O)OCC(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 BGYHLZZASRKEJE-UHFFFAOYSA-N 0.000 description 7
- 230000000052 comparative effect Effects 0.000 description 6
- 150000002148 esters Chemical class 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 230000032683 aging Effects 0.000 description 4
- 239000003054 catalyst Substances 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 4
- SEFYJVFBMNOLBK-UHFFFAOYSA-N 2-[2-[2-(oxiran-2-ylmethoxy)ethoxy]ethoxymethyl]oxirane Chemical compound C1OC1COCCOCCOCC1CO1 SEFYJVFBMNOLBK-UHFFFAOYSA-N 0.000 description 3
- WPMYUUITDBHVQZ-UHFFFAOYSA-N 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoic acid Chemical compound CC(C)(C)C1=CC(CCC(O)=O)=CC(C(C)(C)C)=C1O WPMYUUITDBHVQZ-UHFFFAOYSA-N 0.000 description 3
- UJAWGGOCYUPCPS-UHFFFAOYSA-N 4-(2-phenylpropan-2-yl)-n-[4-(2-phenylpropan-2-yl)phenyl]aniline Chemical compound C=1C=C(NC=2C=CC(=CC=2)C(C)(C)C=2C=CC=CC=2)C=CC=1C(C)(C)C1=CC=CC=C1 UJAWGGOCYUPCPS-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- CWERGRDVMFNCDR-UHFFFAOYSA-N alpha-mercaptoacetic acid Natural products OC(=O)CS CWERGRDVMFNCDR-UHFFFAOYSA-N 0.000 description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- LZFNKJKBRGFWDU-UHFFFAOYSA-N 3,6-dioxabicyclo[6.3.1]dodeca-1(12),8,10-triene-2,7-dione Chemical group O=C1OCCOC(=O)C2=CC=CC1=C2 LZFNKJKBRGFWDU-UHFFFAOYSA-N 0.000 description 2
- ZVSXNPBSZYQDKJ-UHFFFAOYSA-N 3,8-dioxabicyclo[8.3.1]tetradeca-1(14),10,12-triene-2,9-dione Chemical group O=C1OCCCCOC(=O)C2=CC=CC1=C2 ZVSXNPBSZYQDKJ-UHFFFAOYSA-N 0.000 description 2
- KERJVHXRZDUVKQ-UHFFFAOYSA-N 4-tert-butyl-2-(5-tert-butyl-2-hydroxyphenyl)sulfanylphenol Chemical compound CC(C)(C)C1=CC=C(O)C(SC=2C(=CC=C(C=2)C(C)(C)C)O)=C1 KERJVHXRZDUVKQ-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- FQYUMYWMJTYZTK-UHFFFAOYSA-N Phenyl glycidyl ether Chemical compound C1OC1COC1=CC=CC=C1 FQYUMYWMJTYZTK-UHFFFAOYSA-N 0.000 description 2
- 239000007983 Tris buffer Substances 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 238000007334 copolymerization reaction Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 230000007062 hydrolysis Effects 0.000 description 2
- 238000006460 hydrolysis reaction Methods 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 239000012778 molding material Substances 0.000 description 2
- NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 description 2
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 2
- 150000003018 phosphorus compounds Chemical class 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 229920000874 polytetramethylene terephthalate Polymers 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- PUZXLFQBRGGQEY-UHFFFAOYSA-N 1,3-dioxonane-4,9-dione Chemical group O=C1CCCCC(=O)OCO1 PUZXLFQBRGGQEY-UHFFFAOYSA-N 0.000 description 1
- XFQHIELVPOKJIM-UHFFFAOYSA-N 1,4-dioxacyclotetradecane-5,14-dione Chemical group O=C1CCCCCCCCC(=O)OCCO1 XFQHIELVPOKJIM-UHFFFAOYSA-N 0.000 description 1
- PAALZGOZEUHCET-UHFFFAOYSA-N 1,4-dioxecane-5,10-dione Chemical group O=C1CCCCC(=O)OCCO1 PAALZGOZEUHCET-UHFFFAOYSA-N 0.000 description 1
- 125000001140 1,4-phenylene group Chemical group [H]C1=C([H])C([*:2])=C([H])C([H])=C1[*:1] 0.000 description 1
- AMCTYGGTIWUNMF-UHFFFAOYSA-N 1,6-dioxacyclohexadecane-7,16-dione Chemical group O=C1CCCCCCCCC(=O)OCCCCO1 AMCTYGGTIWUNMF-UHFFFAOYSA-N 0.000 description 1
- DQVKSODCEUXVCS-UHFFFAOYSA-N 1-(1-octadecylsulfanylethylsulfanyl)octadecane Chemical compound CCCCCCCCCCCCCCCCCCSC(C)SCCCCCCCCCCCCCCCCCC DQVKSODCEUXVCS-UHFFFAOYSA-N 0.000 description 1
- UWFRVQVNYNPBEF-UHFFFAOYSA-N 1-(2,4-dimethylphenyl)propan-1-one Chemical compound CCC(=O)C1=CC=C(C)C=C1C UWFRVQVNYNPBEF-UHFFFAOYSA-N 0.000 description 1
- DFRUTCAWYNEDOW-UHFFFAOYSA-N 1-(dodecylsulfanylmethylsulfanyl)dodecane Chemical compound CCCCCCCCCCCCSCSCCCCCCCCCCCC DFRUTCAWYNEDOW-UHFFFAOYSA-N 0.000 description 1
- IHWDIGHWDQPQMQ-UHFFFAOYSA-N 1-octadecylsulfanyloctadecane Chemical compound CCCCCCCCCCCCCCCCCCSCCCCCCCCCCCCCCCCCC IHWDIGHWDQPQMQ-UHFFFAOYSA-N 0.000 description 1
- ICKWICRCANNIBI-UHFFFAOYSA-N 2,4-di-tert-butylphenol Chemical compound CC(C)(C)C1=CC=C(O)C(C(C)(C)C)=C1 ICKWICRCANNIBI-UHFFFAOYSA-N 0.000 description 1
- OPLCSTZDXXUYDU-UHFFFAOYSA-N 2,4-dimethyl-6-tert-butylphenol Chemical compound CC1=CC(C)=C(O)C(C(C)(C)C)=C1 OPLCSTZDXXUYDU-UHFFFAOYSA-N 0.000 description 1
- DKCPKDPYUFEZCP-UHFFFAOYSA-N 2,6-di-tert-butylphenol Chemical compound CC(C)(C)C1=CC=CC(C(C)(C)C)=C1O DKCPKDPYUFEZCP-UHFFFAOYSA-N 0.000 description 1
- CJBVGVDGFXKBJU-UHFFFAOYSA-N 2,6-ditert-butyl-4-(diphenoxyphosphorylmethyl)phenol Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CP(=O)(OC=2C=CC=CC=2)OC=2C=CC=CC=2)=C1 CJBVGVDGFXKBJU-UHFFFAOYSA-N 0.000 description 1
- LKMJVFRMDSNFRT-UHFFFAOYSA-N 2-(methoxymethyl)oxirane Chemical compound COCC1CO1 LKMJVFRMDSNFRT-UHFFFAOYSA-N 0.000 description 1
- JLTJAOURJZHBKM-UHFFFAOYSA-N 2-hydroxy-n-octadecyl-2-sulfanylacetamide Chemical compound CCCCCCCCCCCCCCCCCCNC(=O)C(O)S JLTJAOURJZHBKM-UHFFFAOYSA-N 0.000 description 1
- MMINFSMURORWKH-UHFFFAOYSA-N 3,6-dioxabicyclo[6.2.2]dodeca-1(10),8,11-triene-2,7-dione Chemical group O=C1OCCOC(=O)C2=CC=C1C=C2 MMINFSMURORWKH-UHFFFAOYSA-N 0.000 description 1
- WSQZNZLOZXSBHA-UHFFFAOYSA-N 3,8-dioxabicyclo[8.2.2]tetradeca-1(12),10,13-triene-2,9-dione Chemical group O=C1OCCCCOC(=O)C2=CC=C1C=C2 WSQZNZLOZXSBHA-UHFFFAOYSA-N 0.000 description 1
- XDILCINHTMZTGG-UHFFFAOYSA-N 3-(3-dodecoxy-3-oxopropyl)sulfanylpropanoic acid Chemical compound CCCCCCCCCCCCOC(=O)CCSCCC(O)=O XDILCINHTMZTGG-UHFFFAOYSA-N 0.000 description 1
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 1
- YTPNQWFYUCOECH-UHFFFAOYSA-N C(CCC)C1=C(C=CC=C1)O.C(C)(C1=C(C(=CC(=C1)C(C)(C)C)C(C)(C)C)O)C1=C(C(=CC(=C1)C(C)(C)C)C(C)(C)C)O Chemical compound C(CCC)C1=C(C=CC=C1)O.C(C)(C1=C(C(=CC(=C1)C(C)(C)C)C(C)(C)C)O)C1=C(C(=CC(=C1)C(C)(C)C)C(C)(C)C)O YTPNQWFYUCOECH-UHFFFAOYSA-N 0.000 description 1
- MHYXFBUAIRLHTO-UHFFFAOYSA-N C(CCCCCCCCCCCCCCCCC)C1=C(C(=C(C(=C1P(O)(O)=O)CCCCCCCCCCCCCCCCCC)C(C)(C)C)O)C(C)(C)C Chemical compound C(CCCCCCCCCCCCCCCCC)C1=C(C(=C(C(=C1P(O)(O)=O)CCCCCCCCCCCCCCCCCC)C(C)(C)C)O)C(C)(C)C MHYXFBUAIRLHTO-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- GKXVJHDEWHKBFH-UHFFFAOYSA-N [2-(aminomethyl)phenyl]methanamine Chemical compound NCC1=CC=CC=C1CN GKXVJHDEWHKBFH-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- LUFPJJNWMYZRQE-UHFFFAOYSA-N benzylsulfanylmethylbenzene Chemical compound C=1C=CC=CC=1CSCC1=CC=CC=C1 LUFPJJNWMYZRQE-UHFFFAOYSA-N 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 125000006267 biphenyl group Chemical group 0.000 description 1
- KKZRJQUSKHOTMO-UHFFFAOYSA-N bis(dodecylsulfanyl)methylbenzene Chemical compound CCCCCCCCCCCCSC(SCCCCCCCCCCCC)C1=CC=CC=C1 KKZRJQUSKHOTMO-UHFFFAOYSA-N 0.000 description 1
- FQUNFJULCYSSOP-UHFFFAOYSA-N bisoctrizole Chemical compound N1=C2C=CC=CC2=NN1C1=CC(C(C)(C)CC(C)(C)C)=CC(CC=2C(=C(C=C(C=2)C(C)(C)CC(C)(C)C)N2N=C3C=CC=CC3=N2)O)=C1O FQUNFJULCYSSOP-UHFFFAOYSA-N 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- LTYMSROWYAPPGB-UHFFFAOYSA-N diphenyl sulfide Chemical compound C=1C=CC=CC=1SC1=CC=CC=C1 LTYMSROWYAPPGB-UHFFFAOYSA-N 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- WNAHIZMDSQCWRP-UHFFFAOYSA-N dodecane-1-thiol Chemical compound CCCCCCCCCCCCS WNAHIZMDSQCWRP-UHFFFAOYSA-N 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 125000004464 hydroxyphenyl group Chemical group 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- AUHZEENZYGFFBQ-UHFFFAOYSA-N mesitylene Substances CC1=CC(C)=CC(C)=C1 AUHZEENZYGFFBQ-UHFFFAOYSA-N 0.000 description 1
- 125000001827 mesitylenyl group Chemical group [H]C1=C(C(*)=C(C([H])=C1C([H])([H])[H])C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 150000002763 monocarboxylic acids Chemical class 0.000 description 1
- WDMJWWMDMSQIGM-UHFFFAOYSA-N n-(2-phenylethyl)butan-1-amine Chemical group CCCCNCCC1=CC=CC=C1 WDMJWWMDMSQIGM-UHFFFAOYSA-N 0.000 description 1
- DLVKRCGYGJZXFK-UHFFFAOYSA-N n-phenyl-2-sulfanylacetamide Chemical compound SCC(=O)NC1=CC=CC=C1 DLVKRCGYGJZXFK-UHFFFAOYSA-N 0.000 description 1
- YSPHRFZMBKXSAX-UHFFFAOYSA-N n-phenyl-3-sulfanylpropanamide Chemical compound SCCC(=O)NC1=CC=CC=C1 YSPHRFZMBKXSAX-UHFFFAOYSA-N 0.000 description 1
- IFUHTURYMZWNNJ-UHFFFAOYSA-N n-phenyl-6-sulfanylhexanamide Chemical compound SCCCCCC(=O)NC1=CC=CC=C1 IFUHTURYMZWNNJ-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- UCUPUEARJPTGKU-UHFFFAOYSA-N octadecyl 3-sulfanylpropanoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CCS UCUPUEARJPTGKU-UHFFFAOYSA-N 0.000 description 1
- LSDVYCAUUPAHPO-UHFFFAOYSA-N octadecyl 6-sulfanylhexanoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CCCCCS LSDVYCAUUPAHPO-UHFFFAOYSA-N 0.000 description 1
- QADJHAOXTKCYFT-UHFFFAOYSA-N octyl 3-(3-octoxy-3-oxopropyl)sulfanylpropanoate Chemical compound CCCCCCCCOC(=O)CCSCCC(=O)OCCCCCCCC QADJHAOXTKCYFT-UHFFFAOYSA-N 0.000 description 1
- FDPIMTJIUBPUKL-UHFFFAOYSA-N pentan-3-one Chemical compound CCC(=O)CC FDPIMTJIUBPUKL-UHFFFAOYSA-N 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 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
- YODZTKMDCQEPHD-UHFFFAOYSA-N thiodiglycol Chemical compound OCCSCCO YODZTKMDCQEPHD-UHFFFAOYSA-N 0.000 description 1
- TUQOTMZNTHZOKS-UHFFFAOYSA-N tributylphosphine Chemical compound CCCCP(CCCC)CCCC TUQOTMZNTHZOKS-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2812683A JPS59152951A (ja) | 1983-02-21 | 1983-02-21 | ポリエステル型ブロツク共重合体組成物 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2812683A JPS59152951A (ja) | 1983-02-21 | 1983-02-21 | ポリエステル型ブロツク共重合体組成物 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS59152951A true JPS59152951A (ja) | 1984-08-31 |
| JPH0427269B2 JPH0427269B2 (enrdf_load_stackoverflow) | 1992-05-11 |
Family
ID=12240090
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2812683A Granted JPS59152951A (ja) | 1983-02-21 | 1983-02-21 | ポリエステル型ブロツク共重合体組成物 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS59152951A (enrdf_load_stackoverflow) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1997030112A1 (en) * | 1996-02-15 | 1997-08-21 | Ciba Specialty Chemicals Holding Inc. | Stabilisation of polyolefin-recyclates |
| JP2001342330A (ja) * | 2000-06-02 | 2001-12-14 | Daicel Chem Ind Ltd | ポリエステルブロック共重合体組成物 |
| EP1498442A3 (en) * | 1999-08-05 | 2005-03-09 | Daicel Chemical Industries, Ltd. | Method for the preparation of a polyester block copolymer, a polyester block copolymer composition and method for the preparation thereof |
| EP1378540A4 (en) * | 2001-04-03 | 2005-04-27 | Daicel Chem | Polyester block copolymer composition |
| WO2007111059A1 (ja) | 2006-03-24 | 2007-10-04 | Daicel Chemical Industries, Ltd. | ポリエステル系樹脂組成物及び成形体 |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS50107044A (enrdf_load_stackoverflow) * | 1974-01-29 | 1975-08-23 | ||
| JPS51111896A (en) * | 1975-03-28 | 1976-10-02 | Teijin Ltd | Hollow articles for medical equipment |
| JPS52108452A (en) * | 1976-03-08 | 1977-09-10 | Toray Ind Inc | Fire-retarding polybutylene terephthalate composition |
| JPS58162654A (ja) * | 1982-03-19 | 1983-09-27 | Toyobo Co Ltd | ポリエステル型ブロツク共重合体組成物 |
-
1983
- 1983-02-21 JP JP2812683A patent/JPS59152951A/ja active Granted
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS50107044A (enrdf_load_stackoverflow) * | 1974-01-29 | 1975-08-23 | ||
| JPS51111896A (en) * | 1975-03-28 | 1976-10-02 | Teijin Ltd | Hollow articles for medical equipment |
| JPS52108452A (en) * | 1976-03-08 | 1977-09-10 | Toray Ind Inc | Fire-retarding polybutylene terephthalate composition |
| JPS58162654A (ja) * | 1982-03-19 | 1983-09-27 | Toyobo Co Ltd | ポリエステル型ブロツク共重合体組成物 |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1997030112A1 (en) * | 1996-02-15 | 1997-08-21 | Ciba Specialty Chemicals Holding Inc. | Stabilisation of polyolefin-recyclates |
| EP1498442A3 (en) * | 1999-08-05 | 2005-03-09 | Daicel Chemical Industries, Ltd. | Method for the preparation of a polyester block copolymer, a polyester block copolymer composition and method for the preparation thereof |
| US7196123B2 (en) | 1999-08-05 | 2007-03-27 | Jun Watanabe | Polyester block copolymer composition and process for the preparation thereof |
| CN100424131C (zh) * | 1999-08-05 | 2008-10-08 | 大赛璐化学工业株式会社 | 聚酯嵌段共聚体组合物及其制备方法 |
| CN100424132C (zh) * | 1999-08-05 | 2008-10-08 | 大赛璐化学工业株式会社 | 聚酯嵌段共聚体组合物 |
| JP2001342330A (ja) * | 2000-06-02 | 2001-12-14 | Daicel Chem Ind Ltd | ポリエステルブロック共重合体組成物 |
| EP1378540A4 (en) * | 2001-04-03 | 2005-04-27 | Daicel Chem | Polyester block copolymer composition |
| WO2007111059A1 (ja) | 2006-03-24 | 2007-10-04 | Daicel Chemical Industries, Ltd. | ポリエステル系樹脂組成物及び成形体 |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0427269B2 (enrdf_load_stackoverflow) | 1992-05-11 |
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