JPWO2013129489A1 - 熱可塑性樹脂組成物 - Google Patents
熱可塑性樹脂組成物 Download PDFInfo
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- JPWO2013129489A1 JPWO2013129489A1 JP2014502317A JP2014502317A JPWO2013129489A1 JP WO2013129489 A1 JPWO2013129489 A1 JP WO2013129489A1 JP 2014502317 A JP2014502317 A JP 2014502317A JP 2014502317 A JP2014502317 A JP 2014502317A JP WO2013129489 A1 JPWO2013129489 A1 JP WO2013129489A1
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- Prior art keywords
- ion
- group
- ammonium
- thermoplastic resin
- carbon atoms
- Prior art date
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- 229920005992 thermoplastic resin Polymers 0.000 title claims abstract description 46
- 239000011342 resin composition Substances 0.000 title claims abstract description 26
- -1 pyrrolinium ion Chemical class 0.000 claims abstract description 635
- 150000002500 ions Chemical class 0.000 claims abstract description 145
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 43
- 239000000126 substance Substances 0.000 claims abstract description 36
- 150000003839 salts Chemical class 0.000 claims abstract description 31
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims abstract description 14
- CZPWVGJYEJSRLH-UHFFFAOYSA-P pyrimidine-1,3-diium Chemical compound C1=C[NH+]=C[NH+]=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-P 0.000 claims abstract description 10
- RAXXELZNTBOGNW-UHFFFAOYSA-O Imidazolium Chemical compound C1=C[NH+]=CN1 RAXXELZNTBOGNW-UHFFFAOYSA-O 0.000 claims abstract description 9
- RWRDLPDLKQPQOW-UHFFFAOYSA-O Pyrrolidinium ion Chemical compound C1CC[NH2+]C1 RWRDLPDLKQPQOW-UHFFFAOYSA-O 0.000 claims abstract description 8
- JUJWROOIHBZHMG-UHFFFAOYSA-O pyridinium Chemical compound C1=CC=[NH+]C=C1 JUJWROOIHBZHMG-UHFFFAOYSA-O 0.000 claims abstract description 8
- 125000002947 alkylene group Chemical group 0.000 claims abstract description 7
- 125000003710 aryl alkyl group Chemical group 0.000 claims abstract description 7
- 125000006165 cyclic alkyl group Chemical group 0.000 claims abstract description 7
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- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 14
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- 125000003118 aryl group Chemical group 0.000 claims description 9
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- XECAHXYUAAWDEL-UHFFFAOYSA-N acrylonitrile butadiene styrene Chemical compound C=CC=C.C=CC#N.C=CC1=CC=CC=C1 XECAHXYUAAWDEL-UHFFFAOYSA-N 0.000 claims description 5
- 239000004676 acrylonitrile butadiene styrene Substances 0.000 claims description 5
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- NQRYJNQNLNOLGT-UHFFFAOYSA-O Piperidinium(1+) Chemical group C1CC[NH2+]CC1 NQRYJNQNLNOLGT-UHFFFAOYSA-O 0.000 claims description 4
- 229910001416 lithium ion Inorganic materials 0.000 claims description 4
- XSCHRSMBECNVNS-UHFFFAOYSA-O quinoxalin-1-ium Chemical compound [NH+]1=CC=NC2=CC=CC=C21 XSCHRSMBECNVNS-UHFFFAOYSA-O 0.000 claims description 4
- 241000534944 Thia Species 0.000 abstract 1
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- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 8
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 8
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- 125000000217 alkyl group Chemical group 0.000 description 5
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- PXKLMJQFEQBVLD-UHFFFAOYSA-N bisphenol F Chemical compound C1=CC(O)=CC=C1CC1=CC=C(O)C=C1 PXKLMJQFEQBVLD-UHFFFAOYSA-N 0.000 description 4
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- BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 4
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- FJKROLUGYXJWQN-UHFFFAOYSA-N 4-hydroxybenzoic acid Chemical compound OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 3
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- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 3
- 239000004743 Polypropylene Substances 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
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- 150000002009 diols Chemical class 0.000 description 3
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- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
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- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 125000001424 substituent group Chemical group 0.000 description 3
- 229920001567 vinyl ester resin Polymers 0.000 description 3
- AFFLGGQVNFXPEV-UHFFFAOYSA-N 1-decene Chemical compound CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 description 2
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 2
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 2
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 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 2
- 125000004204 2-methoxyphenyl group Chemical group [H]C1=C([H])C(*)=C(OC([H])([H])[H])C([H])=C1[H] 0.000 description 2
- URFNSYWAGGETFK-UHFFFAOYSA-N 4,4'-Dihydroxybibenzyl Chemical compound C1=CC(O)=CC=C1CCC1=CC=C(O)C=C1 URFNSYWAGGETFK-UHFFFAOYSA-N 0.000 description 2
- VPWNQTHUCYMVMZ-UHFFFAOYSA-N 4,4'-sulfonyldiphenol Chemical compound C1=CC(O)=CC=C1S(=O)(=O)C1=CC=C(O)C=C1 VPWNQTHUCYMVMZ-UHFFFAOYSA-N 0.000 description 2
- AQIIVEISJBBUCR-UHFFFAOYSA-N 4-(3-phenylpropyl)pyridine Chemical compound C=1C=NC=CC=1CCCC1=CC=CC=C1 AQIIVEISJBBUCR-UHFFFAOYSA-N 0.000 description 2
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- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 2
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- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920001195 polyisoprene Polymers 0.000 description 1
- 239000002861 polymer material Substances 0.000 description 1
- 239000003505 polymerization initiator Substances 0.000 description 1
- 229920005629 polypropylene homopolymer Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920005990 polystyrene resin Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 229920001290 polyvinyl ester Polymers 0.000 description 1
- 239000005033 polyvinylidene chloride Substances 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- SCUZVMOVTVSBLE-UHFFFAOYSA-N prop-2-enenitrile;styrene Chemical compound C=CC#N.C=CC1=CC=CC=C1 SCUZVMOVTVSBLE-UHFFFAOYSA-N 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- YPFDHNVEDLHUCE-UHFFFAOYSA-N propane-1,3-diol Chemical compound OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 1
- 125000001325 propanoyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229960000380 propiolactone Drugs 0.000 description 1
- WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical compound CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- ROSDSFDQCJNGOL-UHFFFAOYSA-N protonated dimethyl amine Natural products CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 1
- NSCBFOVRSLSEIW-UHFFFAOYSA-O pyrazin-1-ium-1-carboxamide Chemical compound NC(=O)[N+]1=CC=NC=C1 NSCBFOVRSLSEIW-UHFFFAOYSA-O 0.000 description 1
- 125000001725 pyrenyl group Chemical group 0.000 description 1
- 238000010526 radical polymerization reaction Methods 0.000 description 1
- 239000002516 radical scavenger Substances 0.000 description 1
- 229920005604 random copolymer Polymers 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000000523 sample Substances 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 229920002379 silicone rubber Polymers 0.000 description 1
- 239000004945 silicone rubber Substances 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 229920003066 styrene-(meth)acrylic acid ester copolymer Polymers 0.000 description 1
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 1
- 150000003462 sulfoxides Chemical class 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 239000008399 tap water Substances 0.000 description 1
- 235000020679 tap water Nutrition 0.000 description 1
- 229920001897 terpolymer Polymers 0.000 description 1
- 125000004213 tert-butoxy group Chemical group [H]C([H])([H])C(O*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 125000001973 tert-pentyl group Chemical group [H]C([H])([H])C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- DZLFLBLQUQXARW-UHFFFAOYSA-N tetrabutylammonium Chemical compound CCCC[N+](CCCC)(CCCC)CCCC DZLFLBLQUQXARW-UHFFFAOYSA-N 0.000 description 1
- 125000001935 tetracenyl group Chemical group C1(=CC=CC2=CC3=CC4=CC=CC=C4C=C3C=C12)* 0.000 description 1
- CBXCPBUEXACCNR-UHFFFAOYSA-N tetraethylammonium Chemical compound CC[N+](CC)(CC)CC CBXCPBUEXACCNR-UHFFFAOYSA-N 0.000 description 1
- QEMXHQIAXOOASZ-UHFFFAOYSA-N tetramethylammonium Chemical compound C[N+](C)(C)C QEMXHQIAXOOASZ-UHFFFAOYSA-N 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
- GJSGYPDDPQRWPK-UHFFFAOYSA-N tetrapentylammonium Chemical compound CCCCC[N+](CCCCC)(CCCCC)CCCCC GJSGYPDDPQRWPK-UHFFFAOYSA-N 0.000 description 1
- OSBSFAARYOCBHB-UHFFFAOYSA-N tetrapropylammonium Chemical compound CCC[N+](CCC)(CCC)CCC OSBSFAARYOCBHB-UHFFFAOYSA-N 0.000 description 1
- 125000003396 thiol group Chemical group [H]S* 0.000 description 1
- 125000003866 trichloromethyl group Chemical group ClC(Cl)(Cl)* 0.000 description 1
- ASLXNOZOXWPTNG-UHFFFAOYSA-N tricosan-1-amine Chemical compound CCCCCCCCCCCCCCCCCCCCCCCN ASLXNOZOXWPTNG-UHFFFAOYSA-N 0.000 description 1
- ABVVEAHYODGCLZ-UHFFFAOYSA-N tridecan-1-amine Chemical compound CCCCCCCCCCCCCN ABVVEAHYODGCLZ-UHFFFAOYSA-N 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-O triethanolammonium Chemical compound OCC[NH+](CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-O 0.000 description 1
- ZMANZCXQSJIPKH-UHFFFAOYSA-O triethylammonium ion Chemical compound CC[NH+](CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-O 0.000 description 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
- WQCRINVIOJTXSE-UHFFFAOYSA-N trimethyl(nonadecyl)azanium Chemical compound CCCCCCCCCCCCCCCCCCC[N+](C)(C)C WQCRINVIOJTXSE-UHFFFAOYSA-N 0.000 description 1
- ZVFDPYZBJGKPII-UHFFFAOYSA-N trimethyl(nonyl)azanium Chemical compound CCCCCCCCC[N+](C)(C)C ZVFDPYZBJGKPII-UHFFFAOYSA-N 0.000 description 1
- FSWHKYOVBASSCG-UHFFFAOYSA-N trimethyl(pentadecyl)azanium Chemical compound CCCCCCCCCCCCCCC[N+](C)(C)C FSWHKYOVBASSCG-UHFFFAOYSA-N 0.000 description 1
- ACZOGADOAZWANS-UHFFFAOYSA-N trimethyl(pentyl)azanium Chemical compound CCCCC[N+](C)(C)C ACZOGADOAZWANS-UHFFFAOYSA-N 0.000 description 1
- GLFDLEXFOHUASB-UHFFFAOYSA-N trimethyl(tetradecyl)azanium Chemical compound CCCCCCCCCCCCCC[N+](C)(C)C GLFDLEXFOHUASB-UHFFFAOYSA-N 0.000 description 1
- QKRNEEOLHKKGMA-UHFFFAOYSA-N trimethyl(tricosyl)azanium Chemical compound CCCCCCCCCCCCCCCCCCCCCCC[N+](C)(C)C QKRNEEOLHKKGMA-UHFFFAOYSA-N 0.000 description 1
- CUHTWKRYGOJCEX-UHFFFAOYSA-N trimethyl(tridecyl)azanium Chemical compound CCCCCCCCCCCCC[N+](C)(C)C CUHTWKRYGOJCEX-UHFFFAOYSA-N 0.000 description 1
- QDUATGYYXKDLEI-UHFFFAOYSA-N trimethyl(undecyl)azanium Chemical compound CCCCCCCCCCC[N+](C)(C)C QDUATGYYXKDLEI-UHFFFAOYSA-N 0.000 description 1
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 1
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- YFTHZRPMJXBUME-UHFFFAOYSA-N tripropylamine Chemical compound CCCN(CCC)CCC YFTHZRPMJXBUME-UHFFFAOYSA-N 0.000 description 1
- QFKMMXYLAPZKIB-UHFFFAOYSA-N undecan-1-amine Chemical compound CCCCCCCCCCCN QFKMMXYLAPZKIB-UHFFFAOYSA-N 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 125000005023 xylyl group Chemical group 0.000 description 1
- PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-Caprolactone Chemical compound O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/30—Sulfur-, selenium- or tellurium-containing compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/32—Polymers modified by chemical after-treatment
- C08G65/329—Polymers modified by chemical after-treatment with organic compounds
- C08G65/334—Polymers modified by chemical after-treatment with organic compounds containing sulfur
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/32—Polymers modified by chemical after-treatment
- C08G65/329—Polymers modified by chemical after-treatment with organic compounds
- C08G65/334—Polymers modified by chemical after-treatment with organic compounds containing sulfur
- C08G65/3344—Polymers modified by chemical after-treatment with organic compounds containing sulfur containing oxygen in addition to sulfur
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/36—Sulfur-, selenium-, or tellurium-containing compounds
- C08K5/41—Compounds containing sulfur bound to oxygen
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L71/00—Compositions of polyethers obtained by reactions forming an ether link in the main chain; Compositions of derivatives of such polymers
- C08L71/02—Polyalkylene oxides
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/30—Sulfur-, selenium- or tellurium-containing compounds
- C08K2003/3045—Sulfates
- C08K2003/3054—Ammonium sulfates
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- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Polyethers (AREA)
Abstract
Description
本発明で用いられる(a)熱可塑性樹脂は、特に制限されないが、例えば、(メタ)アクリル樹脂、スチレン樹脂、オレフィン樹脂(環状オレフィン樹脂を含む)、ポリエステル樹脂、ポリカーボネート樹脂、ポリアミド樹脂、ポリフェニレンエーテル樹脂、ポリフェニレンスルフィド樹脂、ハロゲン含有樹脂(ポリ塩化ビニル、ポリ塩化ビニリデン、フッ素樹脂など)、ポリスルホン樹脂(ポリエーテルスルホン、ポリスルホンなど)、セルロース誘導体(セルロースエステル類、セルロースカーバメート類、セルロースエーテル類など)、シリコーン樹脂(ポリジメチルシロキサン、ポリメチルフェニルシロキサンなど)、ポリ酢酸ビニルなどのポリビニルエステル樹脂、ポリビニルアルコール樹脂およびこれらの誘導体樹脂、ゴムまたはエラストマー(ポリブタジエン、ポリイソプレンなどのジエンゴム、スチレン−ブタジエン共重合体、アクリロニトリル−ブタジエン共重合体、アクリロニトリル−ブタジエン−スチレン共重合体(ABS樹脂)、アクリルゴム、ウレタンゴム、シリコーンゴムなど)などが挙げられる。上記熱可塑性樹脂は、単独でもまたは2種以上組み合わせても使用することができる。
本発明で用いられる(b)イオン結合性塩(以下、単に成分(b)とも称する)は、前記化学式(1)または前記化学式(2)で表される化合物である。該イオン結合性塩は、単独でもまたは2種以上組み合わせて用いてもよい。
本発明の熱可塑性樹脂組成物の製造方法は、特に制限されず、例えば、上記成分(a)、成分(b)、および必要に応じて他の添加剤を溶融混練する方法が挙げられる。溶融混練の方法は特に制限がなく、例えば、単軸押出機、二軸押出機、熱ロール、バンバリーミキサー、ヘンシェルミキサー、タンブラーミキサー、または各種ニーダー等の装置を使用する方法を採用することができる。
本発明の熱可塑性樹脂組成物の用途としては、例えば、塗料、接着剤、粘着剤、繊維助剤、製紙用途(表面コート剤など)、土木用途(コンクリート混和剤など)等が挙げられる。
ドデシルベンゼンスルホン酸(o−,m−,p−ドデシルベンゼンスルホン酸異性体混合物)(テイカ株式会社製、商品名:テイカトックス120、略称:DB−SO3H)326.5質量部に、N−モノエチルエタノールアミン(日本乳化剤株式会社製、商品名:アミノアルコールMEM、略称:MEM)93.6質量部を滴下した後、1時間反応させた。反応後、過剰のMEMを減圧留去して目的とするイオン結合性塩(略称:[MEM][DB−SO3]、前記化学式(8)で表される化合物)を415.6質量部得た。
DB−SO3Hの代わりに、ポリオキシエチレン多環フェニルエーテル硫酸エステルアンモニウム塩の30%水溶液(日本乳化剤株式会社製、商品名:ニューコール707−SF、略称:N−707−SF)を減圧留去して得られたポリオキシエチレン多環フェニルエーテル硫酸エステルアンモニウム塩(略称:707−SF)を920.1質量部を用いたこと以外は、合成例1と同様にして、目的とするイオン結合性塩(略称:[MEM][N−707−S]、前記化学式(3)で表される化合物)を992.2質量部得た。
DB−SO3Hの代わりに、従来公知の方法により合成したポリオキシエチレントリデシルエーテル硫酸エステルアンモニウム塩(略称:1305−SF)517.4質量部を用いたこと以外は、合成例1と同様にして、目的とするイオン結合性塩(略称:[MEM][N−1305−S]、前記化学式(4)で表される化合物)を589.5質量部得た。
DB−SO3Hの代わりに、従来公知の方法により合成したポリオキシエチレントリデシルエーテル硫酸エステルアンモニウム塩(略称:1310−SF)738.0質量部を用いたこと以外は、合成例1と同様にして、目的とするイオン結合性塩(略称:[MEM][N−1310−S]、前記化学式(5)で表される化合物)を810.1質量部得た。
DB−SO3Hの代わりに、従来公知の方法により合成したポリオキシエチレンアルキルエーテル硫酸エステルアンモニウム塩(略称:2320−SF)1170.0質量部を用いたこと以外は、合成例1と同様にして、目的とするイオン結合性塩(略称:[MEM][N−2320−S]、前記化学式(6)で表される化合物)を1242.1質量部得た。
冷却管、窒素導入管、温度計、テフロン半月攪拌翼を備えたフラスコに、水 100.0質量部を仕込み、80℃まで昇温した。別途、三角フラスコにアクリル酸n−ブチル 50.0質量部、メタクリル酸メチル 35.0質量部、スチレン 15.0質量部、アクリル酸 2.0質量部、乳化剤として上記合成例1で合成した[MEM][DB−SO3] 2.04質量部、水 86.3質量部、10%ペルオキソ二硫酸アンモニウム水溶液 5.1質量部を仕込み、混合し混合物を得た。この混合物を、冷却管等を備えた上記フラスコに15.7質量部仕込み、80℃に昇温して30分間の初期重合を行った。その後3時間かけて三角フラスコ中の混合物を80℃で滴下した。さらに80℃で1時間熟成を行い、28%アンモニア水1.1質量部を使用して中和し、エマルジョンを得た。
[MEM][DB−SO3]の代わりに上記合成例2で得られた[MEM][N−707−S]2.04質量部を混合したことを除いては、実施例1と同様にしてエマルジョンを得た。
[MEM][DB−SO3]の代わりに上記合成例3で得られた[MEM][N−1305−S]2.04質量部を混合したことを除いては、実施例1と同様にしてエマルジョンを得た。
[MEM][DB−SO3]の代わりに上記合成例4で得られた[MEM][N−1310−S]2.04質量部を混合したことを除いては、実施例1と同様にしてエマルジョンを得た。
[MEM][DB−SO3]の代わりに上記合成例5で得られた[MEM][N−2320−S]2.04質量部を混合したことを除いては、実施例1と同様にしてエマルジョンを得た。
[MEM][DB−SO3]の代わりにDB−SO3H 2.04質量部を混合したことを除いては、実施例1と同様にしてエマルジョンを得た。
[MEM][DB−SO3]の代わりに707−SF 2.04質量部を混合したことを除いては、実施例1と同様にしてエマルジョンを得た。
[MEM][DB−SO3]の代わりに1305−SF 2.04質量部を混合したことを除いては、実施例1と同様にしてエマルジョンを得た。
[MEM][DB−SO3]の代わりに1310−SF 2.04質量部を混合したことを除いては、実施例1と同様にしてエマルジョンを得た。
[MEM][DB−SO3]の代わりに2320−SF 2.04質量部を混合したことを除いては、実施例1と同様にしてエマルジョンを得た。
[pHおよび粘度]
得られたエマルジョンのpHは、HORIBA製 pH METER F−51を用いて測定した。また、得られたエマルジョンの粘度は、TOKIMEC製 VISCOMETER BL型粘度計を用いて測定した。
初期乳化安定性は、プレエマルジョンを10分間静置した後の液状態を目視で観察し、以下のように評価した。
×:分層する
重合安定性は、乳化重合後の濾過残渣質量/エマルジョン中の固形分質量の百分率で表した。
耐水性は、作製した試験片を水に24時間浸漬させた後の塗膜の状態を確認し、以下のように評価した。
◎:全体が透明
○:部分的に青白濁
△:全体が青白濁
×:全体が白濁
剥離の有無(密着性)
◎:剥離なし(指で擦っても剥離せず)
○:剥離なし(指で擦ると剥離する)
△:部分的に剥離
×:全体が剥離
[帯電防止性試験(表面固有抵抗率)]
試験片作製後の表面固有抵抗率を株式会社三菱化学アナリテック製 高抵抗率計ハイレスターUPおよびURSプローブを用い、印加電圧250Vにて測定した。また、試験片に水道水を30秒間流水(約1L)させ、次いでイオン交換水ですすぎ、水滴を拭き取った後に110℃で5分間乾燥させた。この工程を1回行った後の試験片の表面固有抵抗率を、上記と同様にして測定した。
試験片を自然曝露(1月間、試験片を南面30°傾斜で屋外曝露)させた後、株式会社堀場製作所製 GLOSS CHECKER IG−331を使用して光沢値を測定した。各試験片について、自然曝露後の光沢値/初期光沢値の百分率を算出し光沢保持率とした。光沢保持率の数値が高いほど、耐候性に優れることを意味する。
Claims (6)
- (a)熱可塑性樹脂と、
(b)下記化学式(1)または下記化学式(2)で表されるイオン結合性塩と、
を含む、熱可塑性樹脂組成物:
- 前記(b)イオン結合性塩の含有量は、前記(a)熱可塑性樹脂100質量部に対して0.1〜20質量部である、請求項1に記載の熱可塑性樹脂組成物。
- 前記(a)熱可塑性樹脂が、(メタ)アクリル樹脂、スチレン樹脂、オレフィン樹脂、ポリエステル樹脂およびアクリロニトリル−ブタジエン−スチレン共重合体(ABS樹脂)からなる群より選択される少なくとも1種である、請求項1または2に記載の熱可塑性樹脂組成物。
- 前記化学式(1)および(2)中のQ1およびQ2は、それぞれ独立して、アンモニウムイオンおよびピペリジニウムイオンからなる群より選択される少なくとも1種である、請求項1〜3のいずれか1項に記載の熱可塑性樹脂組成物。
- 前記(a)熱可塑性樹脂がアクリロニトリル−ブタジエン−スチレン共重合体(ABS樹脂)であり、前記(b)イオン結合性塩が前記化学式(2)で表されるものである、請求項1〜4のいずれか1項に記載の熱可塑性樹脂組成物。
- エマルジョンの形態である、請求項1〜5のいずれか1項に記載の熱可塑性樹脂組成物。
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JP5457596B1 (ja) | 2013-07-19 | 2014-04-02 | 日本乳化剤株式会社 | Abs樹脂組成物用帯電防止剤およびabs樹脂組成物 |
WO2016084954A1 (ja) * | 2014-11-28 | 2016-06-02 | 日本乳化剤株式会社 | 熱可塑性樹脂用帯電防止剤および熱可塑性樹脂組成物 |
JP6816431B2 (ja) * | 2016-09-29 | 2021-01-20 | 東レ株式会社 | イオン塩、それを含有する熱可塑性樹脂組成物およびその製造方法 |
JP6791554B2 (ja) * | 2016-12-14 | 2020-11-25 | 花王株式会社 | 耐水塗膜用ポリマーエマルションの製造方法 |
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