JP6521201B1 - 回転成形用ポリアミド樹脂組成物及びそれを用いた回転成形品 - Google Patents
回転成形用ポリアミド樹脂組成物及びそれを用いた回転成形品 Download PDFInfo
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- JP6521201B1 JP6521201B1 JP2018568461A JP2018568461A JP6521201B1 JP 6521201 B1 JP6521201 B1 JP 6521201B1 JP 2018568461 A JP2018568461 A JP 2018568461A JP 2018568461 A JP2018568461 A JP 2018568461A JP 6521201 B1 JP6521201 B1 JP 6521201B1
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- acid
- polyamide
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- polyamide resin
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- 229920006122 polyamide resin Polymers 0.000 title claims abstract description 61
- 239000011342 resin composition Substances 0.000 title claims abstract description 57
- 238000001175 rotational moulding Methods 0.000 title claims abstract description 29
- 229920000098 polyolefin Polymers 0.000 claims abstract description 39
- 239000004953 Aliphatic polyamide Substances 0.000 claims abstract description 15
- 229920003231 aliphatic polyamide Polymers 0.000 claims abstract description 15
- 229920000642 polymer Polymers 0.000 claims abstract description 11
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims abstract description 10
- 229920006012 semi-aromatic polyamide Polymers 0.000 claims description 42
- 239000004711 α-olefin Substances 0.000 claims description 27
- 229920000089 Cyclic olefin copolymer Polymers 0.000 claims description 23
- 229920002292 Nylon 6 Polymers 0.000 claims description 12
- -1 polyethylene Polymers 0.000 description 170
- 239000004952 Polyamide Substances 0.000 description 95
- 229920002647 polyamide Polymers 0.000 description 95
- 229920001577 copolymer Polymers 0.000 description 30
- 238000006116 polymerization reaction Methods 0.000 description 28
- 238000000034 method Methods 0.000 description 26
- GVNWZKBFMFUVNX-UHFFFAOYSA-N Adipamide Chemical compound NC(=O)CCCCC(N)=O GVNWZKBFMFUVNX-UHFFFAOYSA-N 0.000 description 25
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 25
- 238000006243 chemical reaction Methods 0.000 description 21
- 125000001142 dicarboxylic acid group Chemical group 0.000 description 19
- 239000003795 chemical substances by application Substances 0.000 description 18
- 125000004432 carbon atom Chemical group C* 0.000 description 17
- 125000004427 diamine group Chemical group 0.000 description 16
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 14
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 14
- 239000000047 product Substances 0.000 description 13
- 239000004698 Polyethylene Substances 0.000 description 12
- 238000004898 kneading Methods 0.000 description 12
- WLJVNTCWHIRURA-UHFFFAOYSA-N pimelic acid Chemical compound OC(=O)CCCCCC(O)=O WLJVNTCWHIRURA-UHFFFAOYSA-N 0.000 description 12
- 229920006111 poly(hexamethylene terephthalamide) Polymers 0.000 description 12
- 239000002994 raw material Substances 0.000 description 12
- 229910052698 phosphorus Inorganic materials 0.000 description 11
- GKXVJHDEWHKBFH-UHFFFAOYSA-N xylylenediamine group Chemical group C=1(C(=CC=CC1)CN)CN GKXVJHDEWHKBFH-UHFFFAOYSA-N 0.000 description 11
- WPWNSTTVSOUHRP-UHFFFAOYSA-N [1-(aminomethyl)naphthalen-2-yl]methanamine Chemical group C1=CC=CC2=C(CN)C(CN)=CC=C21 WPWNSTTVSOUHRP-UHFFFAOYSA-N 0.000 description 10
- 239000002253 acid Substances 0.000 description 10
- 239000003963 antioxidant agent Substances 0.000 description 10
- VHRGRCVQAFMJIZ-UHFFFAOYSA-N cadaverine Chemical compound NCCCCCN VHRGRCVQAFMJIZ-UHFFFAOYSA-N 0.000 description 10
- 239000000203 mixture Substances 0.000 description 10
- BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 10
- 239000011574 phosphorus Substances 0.000 description 10
- 229920000052 poly(p-xylylene) Polymers 0.000 description 10
- 229920000573 polyethylene Polymers 0.000 description 10
- KIDHWZJUCRJVML-UHFFFAOYSA-N putrescine Chemical compound NCCCCN KIDHWZJUCRJVML-UHFFFAOYSA-N 0.000 description 10
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 10
- LWBHHRRTOZQPDM-UHFFFAOYSA-N undecanedioic acid Chemical compound OC(=O)CCCCCCCCCC(O)=O LWBHHRRTOZQPDM-UHFFFAOYSA-N 0.000 description 10
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 9
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 9
- 125000001931 aliphatic group Chemical group 0.000 description 9
- 150000001412 amines Chemical class 0.000 description 9
- 150000004985 diamines Chemical class 0.000 description 9
- ILRSCQWREDREME-UHFFFAOYSA-N dodecanamide Chemical compound CCCCCCCCCCCC(N)=O ILRSCQWREDREME-UHFFFAOYSA-N 0.000 description 9
- 229920001519 homopolymer Polymers 0.000 description 9
- 230000000379 polymerizing effect Effects 0.000 description 9
- 230000009257 reactivity Effects 0.000 description 9
- 229920006121 Polyxylylene adipamide Polymers 0.000 description 8
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 8
- 239000007789 gas Substances 0.000 description 8
- QQHJDPROMQRDLA-UHFFFAOYSA-N hexadecanedioic acid Chemical compound OC(=O)CCCCCCCCCCCCCCC(O)=O QQHJDPROMQRDLA-UHFFFAOYSA-N 0.000 description 8
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 8
- 238000004519 manufacturing process Methods 0.000 description 8
- 239000000178 monomer Substances 0.000 description 8
- BNJOQKFENDDGSC-UHFFFAOYSA-N octadecanedioic acid Chemical compound OC(=O)CCCCCCCCCCCCCCCCC(O)=O BNJOQKFENDDGSC-UHFFFAOYSA-N 0.000 description 8
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 8
- TYFQFVWCELRYAO-UHFFFAOYSA-N suberic acid Chemical compound OC(=O)CCCCCCC(O)=O TYFQFVWCELRYAO-UHFFFAOYSA-N 0.000 description 8
- MHSKRLJMQQNJNC-UHFFFAOYSA-N terephthalamide Chemical compound NC(=O)C1=CC=C(C(N)=O)C=C1 MHSKRLJMQQNJNC-UHFFFAOYSA-N 0.000 description 8
- XFNJVJPLKCPIBV-UHFFFAOYSA-N trimethylenediamine Chemical compound NCCCN XFNJVJPLKCPIBV-UHFFFAOYSA-N 0.000 description 8
- PGGROMGHWHXWJL-UHFFFAOYSA-N 4-(azepane-1-carbonyl)benzamide Chemical compound C1=CC(C(=O)N)=CC=C1C(=O)N1CCCCCC1 PGGROMGHWHXWJL-UHFFFAOYSA-N 0.000 description 7
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 7
- 239000005977 Ethylene Substances 0.000 description 7
- 239000001361 adipic acid Substances 0.000 description 7
- 235000011037 adipic acid Nutrition 0.000 description 7
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 7
- 125000004202 aminomethyl group Chemical group [H]N([H])C([H])([H])* 0.000 description 7
- 125000003118 aryl group Chemical group 0.000 description 7
- 150000001735 carboxylic acids Chemical class 0.000 description 7
- 238000000465 moulding Methods 0.000 description 7
- KYTZHLUVELPASH-UHFFFAOYSA-N naphthalene-1,2-dicarboxylic acid Chemical group C1=CC=CC2=C(C(O)=O)C(C(=O)O)=CC=C21 KYTZHLUVELPASH-UHFFFAOYSA-N 0.000 description 7
- ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 description 7
- PBLZLIFKVPJDCO-UHFFFAOYSA-N 12-aminododecanoic acid Chemical compound NCCCCCCCCCCCC(O)=O PBLZLIFKVPJDCO-UHFFFAOYSA-N 0.000 description 6
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 6
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 6
- BTZVDPWKGXMQFW-UHFFFAOYSA-N Pentadecanedioic acid Chemical compound OC(=O)CCCCCCCCCCCCCC(O)=O BTZVDPWKGXMQFW-UHFFFAOYSA-N 0.000 description 6
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 6
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 6
- 229910052783 alkali metal Inorganic materials 0.000 description 6
- 150000001339 alkali metal compounds Chemical class 0.000 description 6
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 6
- 230000003078 antioxidant effect Effects 0.000 description 6
- QMKYBPDZANOJGF-UHFFFAOYSA-N benzene-1,3,5-tricarboxylic acid Chemical compound OC(=O)C1=CC(C(O)=O)=CC(C(O)=O)=C1 QMKYBPDZANOJGF-UHFFFAOYSA-N 0.000 description 6
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 6
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 description 6
- PAFZNILMFXTMIY-UHFFFAOYSA-N cyclohexylamine Chemical compound NC1CCCCC1 PAFZNILMFXTMIY-UHFFFAOYSA-N 0.000 description 6
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 6
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 6
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 6
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 6
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 6
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 6
- CBFCDTFDPHXCNY-UHFFFAOYSA-N icosane Chemical compound CCCCCCCCCCCCCCCCCCCC CBFCDTFDPHXCNY-UHFFFAOYSA-N 0.000 description 6
- NFVUAUVSFDFOJT-UHFFFAOYSA-N octanediamide Chemical compound NC(=O)CCCCCCC(N)=O NFVUAUVSFDFOJT-UHFFFAOYSA-N 0.000 description 6
- ACVYVLVWPXVTIT-UHFFFAOYSA-N phosphinic acid Chemical compound O[PH2]=O ACVYVLVWPXVTIT-UHFFFAOYSA-N 0.000 description 6
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 6
- 230000000704 physical effect Effects 0.000 description 6
- 229920000768 polyamine Polymers 0.000 description 6
- SCVFZCLFOSHCOH-UHFFFAOYSA-M potassium acetate Chemical compound [K+].CC([O-])=O SCVFZCLFOSHCOH-UHFFFAOYSA-M 0.000 description 6
- 239000007790 solid phase Substances 0.000 description 6
- HQHCYKULIHKCEB-UHFFFAOYSA-N tetradecanedioic acid Chemical compound OC(=O)CCCCCCCCCCCCC(O)=O HQHCYKULIHKCEB-UHFFFAOYSA-N 0.000 description 6
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 description 6
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 5
- 125000003277 amino group Chemical group 0.000 description 5
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 5
- YQLZOAVZWJBZSY-UHFFFAOYSA-N decane-1,10-diamine Chemical compound NCCCCCCCCCCN YQLZOAVZWJBZSY-UHFFFAOYSA-N 0.000 description 5
- 150000001993 dienes Chemical class 0.000 description 5
- 238000011156 evaluation Methods 0.000 description 5
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 5
- 238000002844 melting Methods 0.000 description 5
- 230000008018 melting Effects 0.000 description 5
- 229910052757 nitrogen Inorganic materials 0.000 description 5
- 239000008188 pellet Substances 0.000 description 5
- 239000002530 phenolic antioxidant Substances 0.000 description 5
- 150000003839 salts Chemical class 0.000 description 5
- SZHOJFHSIKHZHA-UHFFFAOYSA-N tridecanoic acid Chemical compound CCCCCCCCCCCCC(O)=O SZHOJFHSIKHZHA-UHFFFAOYSA-N 0.000 description 5
- PWGJDPKCLMLPJW-UHFFFAOYSA-N 1,8-diaminooctane Chemical compound NCCCCCCCCN PWGJDPKCLMLPJW-UHFFFAOYSA-N 0.000 description 4
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 4
- GQEZCXVZFLOKMC-UHFFFAOYSA-N 1-hexadecene Chemical compound CCCCCCCCCCCCCCC=C GQEZCXVZFLOKMC-UHFFFAOYSA-N 0.000 description 4
- RTBFRGCFXZNCOE-UHFFFAOYSA-N 1-methylsulfonylpiperidin-4-one Chemical compound CS(=O)(=O)N1CCC(=O)CC1 RTBFRGCFXZNCOE-UHFFFAOYSA-N 0.000 description 4
- QFGCFKJIPBRJGM-UHFFFAOYSA-N 12-[(2-methylpropan-2-yl)oxy]-12-oxododecanoic acid Chemical compound CC(C)(C)OC(=O)CCCCCCCCCCC(O)=O QFGCFKJIPBRJGM-UHFFFAOYSA-N 0.000 description 4
- DPQHRXRAZHNGRU-UHFFFAOYSA-N 2,4,4-trimethylhexane-1,6-diamine Chemical compound NCC(C)CC(C)(C)CCN DPQHRXRAZHNGRU-UHFFFAOYSA-N 0.000 description 4
- JZUHIOJYCPIVLQ-UHFFFAOYSA-N 2-methylpentane-1,5-diamine Chemical compound NCC(C)CCCN JZUHIOJYCPIVLQ-UHFFFAOYSA-N 0.000 description 4
- FQLAJSQGBDYBAL-UHFFFAOYSA-N 3-(azepane-1-carbonyl)benzamide Chemical compound NC(=O)C1=CC=CC(C(=O)N2CCCCCC2)=C1 FQLAJSQGBDYBAL-UHFFFAOYSA-N 0.000 description 4
- FJSUFIIJYXMJQO-UHFFFAOYSA-N 3-methylpentane-1,5-diamine Chemical compound NCCC(C)CCN FJSUFIIJYXMJQO-UHFFFAOYSA-N 0.000 description 4
- MBRGOFWKNLPACT-UHFFFAOYSA-N 5-methylnonane-1,9-diamine Chemical compound NCCCCC(C)CCCCN MBRGOFWKNLPACT-UHFFFAOYSA-N 0.000 description 4
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 4
- 239000005635 Caprylic acid (CAS 124-07-2) Substances 0.000 description 4
- KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical compound NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 description 4
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 4
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 4
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 4
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 4
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 4
- FDLQZKYLHJJBHD-UHFFFAOYSA-N [3-(aminomethyl)phenyl]methanamine Chemical compound NCC1=CC=CC(CN)=C1 FDLQZKYLHJJBHD-UHFFFAOYSA-N 0.000 description 4
- 150000008065 acid anhydrides Chemical class 0.000 description 4
- 125000002723 alicyclic group Chemical group 0.000 description 4
- JFCQEDHGNNZCLN-UHFFFAOYSA-N anhydrous glutaric acid Natural products OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 description 4
- 150000004984 aromatic diamines Chemical class 0.000 description 4
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 4
- 229910000389 calcium phosphate Inorganic materials 0.000 description 4
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- XBZSBBLNHFMTEB-UHFFFAOYSA-N cyclohexane-1,3-dicarboxylic acid Chemical compound OC(=O)C1CCCC(C(O)=O)C1 XBZSBBLNHFMTEB-UHFFFAOYSA-N 0.000 description 4
- QFTYSVGGYOXFRQ-UHFFFAOYSA-N dodecane-1,12-diamine Chemical compound NCCCCCCCCCCCCN QFTYSVGGYOXFRQ-UHFFFAOYSA-N 0.000 description 4
- PWSKHLMYTZNYKO-UHFFFAOYSA-N heptane-1,7-diamine Chemical compound NCCCCCCCN PWSKHLMYTZNYKO-UHFFFAOYSA-N 0.000 description 4
- 150000003951 lactams Chemical class 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- RXOHFPCZGPKIRD-UHFFFAOYSA-N naphthalene-2,6-dicarboxylic acid Chemical compound C1=C(C(O)=O)C=CC2=CC(C(=O)O)=CC=C21 RXOHFPCZGPKIRD-UHFFFAOYSA-N 0.000 description 4
- WPUMVKJOWWJPRK-UHFFFAOYSA-N naphthalene-2,7-dicarboxylic acid Chemical compound C1=CC(C(O)=O)=CC2=CC(C(=O)O)=CC=C21 WPUMVKJOWWJPRK-UHFFFAOYSA-N 0.000 description 4
- SXJVFQLYZSNZBT-UHFFFAOYSA-N nonane-1,9-diamine Chemical compound NCCCCCCCCCN SXJVFQLYZSNZBT-UHFFFAOYSA-N 0.000 description 4
- 229960002446 octanoic acid Drugs 0.000 description 4
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 4
- 239000001294 propane Substances 0.000 description 4
- WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical compound CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 description 4
- CYIDZMCFTVVTJO-UHFFFAOYSA-N pyromellitic acid Chemical compound OC(=O)C1=CC(C(O)=O)=C(C(O)=O)C=C1C(O)=O CYIDZMCFTVVTJO-UHFFFAOYSA-N 0.000 description 4
- 150000003335 secondary amines Chemical class 0.000 description 4
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 4
- BPSKTAWBYDTMAN-UHFFFAOYSA-N tridecane-1,13-diamine Chemical compound NCCCCCCCCCCCCCN BPSKTAWBYDTMAN-UHFFFAOYSA-N 0.000 description 4
- ARCGXLSVLAOJQL-UHFFFAOYSA-N trimellitic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C(C(O)=O)=C1 ARCGXLSVLAOJQL-UHFFFAOYSA-N 0.000 description 4
- KLNPWTHGTVSSEU-UHFFFAOYSA-N undecane-1,11-diamine Chemical compound NCCCCCCCCCCCN KLNPWTHGTVSSEU-UHFFFAOYSA-N 0.000 description 4
- PXGZQGDTEZPERC-UHFFFAOYSA-N 1,4-cyclohexanedicarboxylic acid Chemical compound OC(=O)C1CCC(C(O)=O)CC1 PXGZQGDTEZPERC-UHFFFAOYSA-N 0.000 description 3
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 description 3
- BMVXCPBXGZKUPN-UHFFFAOYSA-N 1-hexanamine Chemical compound CCCCCCN BMVXCPBXGZKUPN-UHFFFAOYSA-N 0.000 description 3
- JCUZDQXWVYNXHD-UHFFFAOYSA-N 2,2,4-trimethylhexane-1,6-diamine Chemical compound NCCC(C)CC(C)(C)CN JCUZDQXWVYNXHD-UHFFFAOYSA-N 0.000 description 3
- DWFUTNJGNBYHNN-UHFFFAOYSA-N 2,2,4-trimethylhexanedioic acid Chemical compound OC(=O)CC(C)CC(C)(C)C(O)=O DWFUTNJGNBYHNN-UHFFFAOYSA-N 0.000 description 3
- RLEQVGMLDNITBW-UHFFFAOYSA-N 2,4,4-trimethylhexanedioic acid Chemical compound OC(=O)C(C)CC(C)(C)CC(O)=O RLEQVGMLDNITBW-UHFFFAOYSA-N 0.000 description 3
- QKHWUKPTSMULMZ-UHFFFAOYSA-N 2-(aminomethyl)-3,3,5-trimethylcyclopentan-1-amine Chemical compound CC1CC(C)(C)C(CN)C1N QKHWUKPTSMULMZ-UHFFFAOYSA-N 0.000 description 3
- JZUMVFMLJGSMRF-UHFFFAOYSA-N 2-Methyladipic acid Chemical compound OC(=O)C(C)CCCC(O)=O JZUMVFMLJGSMRF-UHFFFAOYSA-N 0.000 description 3
- RNLHGQLZWXBQNY-UHFFFAOYSA-N 3-(aminomethyl)-3,5,5-trimethylcyclohexan-1-amine Chemical compound CC1(C)CC(N)CC(C)(CN)C1 RNLHGQLZWXBQNY-UHFFFAOYSA-N 0.000 description 3
- WVDRSXGPQWNUBN-UHFFFAOYSA-N 4-(4-carboxyphenoxy)benzoic acid Chemical compound C1=CC(C(=O)O)=CC=C1OC1=CC=C(C(O)=O)C=C1 WVDRSXGPQWNUBN-UHFFFAOYSA-N 0.000 description 3
- IGSBHTZEJMPDSZ-UHFFFAOYSA-N 4-[(4-amino-3-methylcyclohexyl)methyl]-2-methylcyclohexan-1-amine Chemical compound C1CC(N)C(C)CC1CC1CC(C)C(N)CC1 IGSBHTZEJMPDSZ-UHFFFAOYSA-N 0.000 description 3
- DZIHTWJGPDVSGE-UHFFFAOYSA-N 4-[(4-aminocyclohexyl)methyl]cyclohexan-1-amine Chemical compound C1CC(N)CCC1CC1CCC(N)CC1 DZIHTWJGPDVSGE-UHFFFAOYSA-N 0.000 description 3
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- PZZICILSCNDOKK-UHFFFAOYSA-N propane-1,2,3-triamine Chemical compound NCC(N)CN PZZICILSCNDOKK-UHFFFAOYSA-N 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 229920001384 propylene homopolymer Polymers 0.000 description 1
- AOHJOMMDDJHIJH-UHFFFAOYSA-N propylenediamine Chemical compound CC(N)CN AOHJOMMDDJHIJH-UHFFFAOYSA-N 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- MWVKGSABHBJPOX-UHFFFAOYSA-N pyridine-2,4,6-triamine Chemical compound NC1=CC(N)=NC(N)=C1 MWVKGSABHBJPOX-UHFFFAOYSA-N 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000007151 ring opening polymerisation reaction Methods 0.000 description 1
- FOGKDYADEBOSPL-UHFFFAOYSA-M rubidium(1+);acetate Chemical compound [Rb+].CC([O-])=O FOGKDYADEBOSPL-UHFFFAOYSA-M 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- AJPJDKMHJJGVTQ-UHFFFAOYSA-M sodium dihydrogen phosphate Chemical compound [Na+].OP(O)([O-])=O AJPJDKMHJJGVTQ-UHFFFAOYSA-M 0.000 description 1
- FQENQNTWSFEDLI-UHFFFAOYSA-J sodium diphosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])([O-])=O FQENQNTWSFEDLI-UHFFFAOYSA-J 0.000 description 1
- 235000019983 sodium metaphosphate Nutrition 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- 229910000162 sodium phosphate Inorganic materials 0.000 description 1
- 235000011008 sodium phosphates Nutrition 0.000 description 1
- 229940048086 sodium pyrophosphate Drugs 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- UUCCCPNEFXQJEL-UHFFFAOYSA-L strontium dihydroxide Chemical compound [OH-].[OH-].[Sr+2] UUCCCPNEFXQJEL-UHFFFAOYSA-L 0.000 description 1
- 229910001866 strontium hydroxide Inorganic materials 0.000 description 1
- RXSHXLOMRZJCLB-UHFFFAOYSA-L strontium;diacetate Chemical compound [Sr+2].CC([O-])=O.CC([O-])=O RXSHXLOMRZJCLB-UHFFFAOYSA-L 0.000 description 1
- 229920001935 styrene-ethylene-butadiene-styrene Polymers 0.000 description 1
- 238000009864 tensile test Methods 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 125000001302 tertiary amino group Chemical group 0.000 description 1
- FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 description 1
- MVGWWCXDTHXKTR-UHFFFAOYSA-J tetralithium;phosphonato phosphate Chemical compound [Li+].[Li+].[Li+].[Li+].[O-]P([O-])(=O)OP([O-])([O-])=O MVGWWCXDTHXKTR-UHFFFAOYSA-J 0.000 description 1
- RYCLIXPGLDDLTM-UHFFFAOYSA-J tetrapotassium;phosphonato phosphate Chemical compound [K+].[K+].[K+].[K+].[O-]P([O-])(=O)OP([O-])([O-])=O RYCLIXPGLDDLTM-UHFFFAOYSA-J 0.000 description 1
- 235000019818 tetrasodium diphosphate Nutrition 0.000 description 1
- 239000001577 tetrasodium phosphonato phosphate Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 150000004992 toluidines Chemical class 0.000 description 1
- 150000003628 tricarboxylic acids Chemical class 0.000 description 1
- TWQULNDIKKJZPH-UHFFFAOYSA-K trilithium;phosphate Chemical compound [Li+].[Li+].[Li+].[O-]P([O-])([O-])=O TWQULNDIKKJZPH-UHFFFAOYSA-K 0.000 description 1
- CELVKTDHZONYFA-UHFFFAOYSA-N trilithium;phosphite Chemical compound [Li+].[Li+].[Li+].[O-]P([O-])[O-] CELVKTDHZONYFA-UHFFFAOYSA-N 0.000 description 1
- VMFOHNMEJNFJAE-UHFFFAOYSA-N trimagnesium;diphosphite Chemical compound [Mg+2].[Mg+2].[Mg+2].[O-]P([O-])[O-].[O-]P([O-])[O-] VMFOHNMEJNFJAE-UHFFFAOYSA-N 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- NCPXQVVMIXIKTN-UHFFFAOYSA-N trisodium;phosphite Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])[O-] NCPXQVVMIXIKTN-UHFFFAOYSA-N 0.000 description 1
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 239000010937 tungsten Substances 0.000 description 1
- QFKMMXYLAPZKIB-UHFFFAOYSA-N undecan-1-amine Chemical compound CCCCCCCCCCCN QFKMMXYLAPZKIB-UHFFFAOYSA-N 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 238000004260 weight control Methods 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L77/00—Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
- C08L77/06—Polyamides derived from polyamines and polycarboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L77/00—Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/26—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers modified by chemical after-treatment
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L77/00—Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
- C08L77/02—Polyamides derived from omega-amino carboxylic acids or from lactams thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/02—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group
- C08L2205/025—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group containing two or more polymers of the same hierarchy C08L, and differing only in parameters such as density, comonomer content, molecular weight, structure
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/03—Polymer mixtures characterised by other features containing three or more polymers in a blend
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- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
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- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
Abstract
Description
(C)成分:190℃、2.16kgの荷重で測定したMFR値が3.0〜30g/10minの未変性ポリオレフィンをc重量部と
を含み、下記式:
50≦c/(b+c)×100≦70
10≦(b+c)/(a+b+c)×100≦40
を満たす回転成形用ポリアミド樹脂組成物及びそれを用いた回転成形品である。
本発明において使用される脂肪族ポリアミドは、主鎖中にアミド結合(−CONH−)を有し、脂肪族ポリアミド構造単位であるラクタム、アミノカルボン酸、又は脂肪族ジアミンと脂肪族ジカルボン酸を原料として、溶融重合、溶液重合や固相重合等の公知の方法で重合、又は共重合することにより得られる。
本発明において使用される変性ポリオレフィンとして、酸変性ポリオレフィン、エポキシ変性ポリオレフィン、グリシジル変性ポリオレフィン等が挙げられる。このうち、特に酸変性ポリオレフィンが好ましい。酸変性ポリオレフィンは、ポリオレフィンを不飽和カルボン酸又はその酸無水物等により酸変性したものである。不飽和カルボン酸又はその酸無水物の具体例としては、マレイン酸、フマル酸、イタコン酸、アクリル酸、メタクリル酸、シス−4−シクロヘキセン−1,2−ジカルボン酸、無水マレイン酸、無水イタコン酸、シス−4−シクロヘキセン−1,2−無水ジカルボン酸等が挙げられる。中でも、無水マレイン酸又は無水イタコン酸が好ましく、無水マレイン酸がより好ましい。不飽和カルボン酸又はその酸無水物の代わりに、酸アミド、酸エステル等の誘導体を用いることもできる。
本発明において使用される未変性ポリオレフィンは、前述の「<(B)成分:変性ポリオレフィン>」項で記載した変性前のポリオレフィンが挙げられる。これらの中でも、エチレン単独重合体、エチレン−α−オレフィン共重合体等のポリエチレンが好ましく、エチレン単独重合体がより好ましい。ポリエチレンとしては、高密度ポリエチレン(HDPE)、中密度ポリエチレン(MDPE)、低密度ポリエチレン(LDPE)、直鎖状低密度ポリエチレン(LLDPE)などが挙げられる。
本発明において好ましく使用される半芳香族ポリアミド樹脂は、芳香族ジカルボン酸と脂肪族ジアミンの共重合体または脂肪族ジカルボン酸と芳香族ジアミンの共重合体である。半芳香族ポリアミド樹脂を用いることにより、耐熱性と低温耐衝撃性が向上する。これらの中でも、全ジアミン単位に対して、炭素原子数6以上13以下の脂肪族ジアミン単位を50モル%以上含むジアミン単位と、全ジカルボン酸単位に対して、テレフタル酸単位、イソフタル酸単位及び/又ナフタレンジカルボン酸単位を50モル%以上含むジカルボン酸単位よりなる共重合体、あるいは、全ジアミン単位に対して、キシリレンジアミン単位及び/又はビス(アミノメチル)ナフタレン単位を50モル%以上含むジアミン単位と、全ジカルボン酸単位に対して、炭素原子数6以上13以下の脂肪族ジカルボン酸単位を50モル%以上含むジカルボン酸単位よりなる共重合体が好ましい。
本発明に係るポリアミド樹脂組成物は、(A)成分であるポリアミド樹脂と、(B)成分である酸変性ポリオレフィンと、(C)成分である未変性ポリオレフィンとを含む。以下、各成分の配合割合の説明において、(A)成分の配合量をa重量部とし、(B)成分の配合量をb重量部とし、(C)成分の配合量をc重量部とする。
50≦c/(b+c)×100≦70
この式を満たすことで、(B)成分と(C)成分がコア−シェル構造を形成するため、得られる回転成形品の表面性及び低温耐衝撃性を両立することができる。c/(b+c)×100が50未満であると、得られるポリアミド樹脂組成物の低温耐衝撃性が低下する。c/(b+c)×100が70を超えると、相分離した未変性ポリオレフィンによって回転成形品の表面性が悪化する。c/(b+c)×100は、53以上であることが好ましく、56以上であることがより好ましい。c/(b+c)×100は、68以下であることが好ましく、66以下であることがより好ましい。
10≦(b+c)/(a+b+c)×100≦40
この式を満たすことで、得られる回転成形品の表面性及び低温耐衝撃性を両立することができる。(b+c)/(a+b+c)×100が10未満であると、得られる回転成形品の低温耐衝撃性が低下してしまう。(b+c)/(a+b+c)×100が40を超えると、得られる回転成形品の表面に粒子形状物が残りやすくなる。c(b+c)/(a+b+c)×100は、15以上であることが好ましく、20以上であることがより好ましい。(b+c)/(a+b+c)×100は、37以下であることが好ましく、34以下であることがより好ましい。
1≦d/(a+b+c+d)×100≦20
この式を満たすことで、得られるポリアミド樹脂組成物の耐熱性を改善することができる。d/(a+b+c+d)×100は、3以上であることが好ましく、5以上であることがより好ましい。d/(a+b+c+d)×100は、18以下であることが好ましく、16以下であることがより好ましい。
本発明に係る回転成形用ポリアミド樹脂組成物は、上記のポリアミド樹脂組成物を用いたものである。本発明に係る回転成形品は、上記の回転成形用ポリアミド樹脂組成物を用いたものである。回転成形法による回転成形用ポリアミド樹脂組成物の成形は、以下の方法で実施することができる。
ポリアミド6(PA6、宇部興産製、商品名:1011FB、ηr=2.20)68.8重量部と、無水マレイン酸変性エチレン−α−オレフィン共重合体(MAH−PEAO、三井化学製、商品名:タフマーMH5020、密度=0.866)10重量部と、未変性ポリエチレン(PE、プライムポリマー製、商品名:エボリューSP0540、MFR値=3.8)13.2重量部と、半芳香族ポリアミド(半芳香族PA、三井・デュポンポリケミカル製、商品名:シーラーPA3426)8.0重量部と、フェノール系酸化防止剤(オルト位にt−ブチル基を有するヒンダードフェノール系酸化防止剤)0.50重量部と、リン系酸化防止剤(オルト位にt−ブチル基を有するフェノールの亜リン酸エステル系酸化防止剤)0.50重量部と、離型剤0.10重量部と、帯電防止剤0.10重量部と、添着Oil0.10重量部とをドライブレンドした。その後、Werner&Pfleiderer製の二軸混練機(商品名:ZSK32Mc+)で溶融混練することで、ポリアミド樹脂組成物のペレットを得た。得られたペレットをシリンダー温度270℃、金型温度80℃で射出成形し、各種試験片を製造し、物性を評価した。得られた結果を表1に示す。
(A)成分の種類及び/又は(A)〜(D)成分の配合比を表1のように変更したこと以外は、実施例1と同様にして、ポリアミド樹脂組成物を得た。なお、実施例3〜6では、(A)成分として実施例1とは異なるポリアミド6(PA6、宇部興産製、商品名:1013B、ηr=2.45)を使用した。比較例3では、(A)成分の代わりに、(A)成分の条件を満たさない(A’)成分として、ポリアミド6(PA6、宇部興産製、商品名:1015B、ηr=2.60)を使用した。比較例4〜5では、(B)成分の代わりに、(B)成分の条件を満たさない(B’)成分として、無水マレイン酸変性エチレン−α−オレフィン共重合体(MAH−PEAO、三井化学製、商品名:タフマーMA9015、密度=0.896)又はマレイン酸変性エチレン−α−オレフィン共重合体(MA−PEAO、三井化学製、商品名:アドマーNB550、密度=0.920)を使用した。比較例6では、(C)成分の代わりに、(C)成分の条件を満たさない(C’)成分として、超高流動ポリエチレン(PE、プライムポリマー製、商品名:NEO−ZEX40300J、MFR値=36)を使用した。
流動性の指標として、キャピラリーレオメーター(東洋精機製、商品名:Capilograph 1D)を用いて、250℃、みかけ剪断速度365[1/sec]の条件で、みかけ粘度ηaを測定し、以下のように評価した。
◎:250未満
○:250〜450
×:450超
表面性の指標として、290℃に設定したホットプレート上にペレットを冷凍粉砕した樹脂粉末を規定量入れたSUS製円筒容器を乗せ、空気下で5分間加熱後取り出すことで得られる成形品の表面を目視にて観察し、以下のように評価した。
◎:表面に凹凸なし
○:表面に凹凸あるものの滑らか
×:表面に凹凸あり、かつ加熱前の粒子形状物が残るなど表面性が悪い
低温耐衝撃性の指標として、ISO 179/1eAに準じて−60℃でのノッチ付きシャルピー衝撃強度を測定し、以下のように評価した。
◎:12kJ/m2超
○:8〜12kJ/m2
×:8kJ/m2未満
低温耐衝撃性の指標として、ISO 527−1,2(引張試験)に準じて23℃での引張破壊呼びひずみを測定し、以下のように評価した。
◎:250%超
○:150〜250%
×:150%未満
耐熱性の指標として、得られたペレットをシリンダー温度270℃、金型温度80℃で射出成形して得た試験片を、空気下200℃に設定したオーブン中で6時間処理した際のΔEを測定した。
Claims (5)
- (A)成分:JIS K6920に従い、96重量%硫酸、ポリマー濃度1重量%、25℃の条件下にて測定した相対粘度ηrが2.60未満の脂肪族ポリアミドをa重量部と、
(B)成分:ASTM D1505に従い測定した密度が0.895g/cm3以下の変性ポリオレフィンをb重量部と、
(C)成分:190℃、2.16kgの荷重で測定したMFR値が3.0〜30g/10minの未変性ポリオレフィンをc重量部と
を含み、下記式:
50≦c/(b+c)×100≦70
10≦(b+c)/(a+b+c)×100≦40
を満たす回転成形用ポリアミド樹脂組成物。 - 前記脂肪族ポリアミドが、ポリアミド6である
請求項1に記載の回転成形用ポリアミド樹脂組成物。 - 前記酸変性ポリオレフィンが、無水マレイン酸変性エチレン−α−オレフィン共重合体である
請求項1又は2に記載の回転成形用ポリアミド樹脂組成物。 - さらに、
(D)成分:半芳香族ポリアミドをd重量部
を含み、下記式:
1≦d/(a+b+c+d)×100≦20
を満たす請求項1〜3のいずれか1項に記載の回転成形用ポリアミド樹脂組成物。 - 請求項1〜4のいずれか1項に記載の回転成形用ポリアミド樹脂組成物を用いた回転成形品。
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EP3950345A4 (en) * | 2019-03-29 | 2022-11-16 | Ube Industries, Ltd. | LAMINATE |
CN114729152B (zh) | 2019-10-30 | 2024-08-27 | Ube株式会社 | 聚酰胺树脂组合物 |
JP7059243B2 (ja) * | 2019-12-16 | 2022-04-25 | Ube株式会社 | 熱可塑成形水素タンクライナー用ポリアミド樹脂成形材料、熱可塑成形水素タンクライナー及び水素タンクの製造方法 |
JP7491072B2 (ja) | 2020-06-11 | 2024-05-28 | Ube株式会社 | ポリアミド樹脂組成物 |
EP4198089A4 (en) | 2020-08-17 | 2024-08-14 | Ube Corp | POLYAMIDE RESIN COMPOSITION |
JP7523341B2 (ja) * | 2020-12-18 | 2024-07-26 | 株式会社ブリヂストン | 炭素繊維複合体、及び炭素繊維複合体の製造方法 |
JPWO2023032780A1 (ja) | 2021-09-01 | 2023-03-09 | ||
CN117916318A (zh) | 2021-09-08 | 2024-04-19 | Ube株式会社 | 聚酰胺树脂组合物 |
DE102021124764A1 (de) | 2021-09-24 | 2023-03-30 | GRAFE Polymer Solutions GmbH | Mikrogranulat zum Rotationsformen und Verfahren zu seiner Herstellung |
WO2024179859A1 (en) | 2023-02-27 | 2024-09-06 | Envalior B.V. | Polyamide composition, process for preparation, process for producing an article, and article made of the composition |
WO2024203169A1 (ja) * | 2023-03-31 | 2024-10-03 | Ube株式会社 | ポリアミド樹脂組成物、それを含むフィルム及びフィルム積層体、並びにペレット混合物 |
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- 2018-08-10 WO PCT/JP2018/030021 patent/WO2019054109A1/ja unknown
- 2018-08-10 CN CN201880058993.4A patent/CN111094454A/zh active Pending
- 2018-08-10 US US16/635,895 patent/US20210139699A1/en not_active Abandoned
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CN111094454A (zh) | 2020-05-01 |
US20210139699A1 (en) | 2021-05-13 |
JP7131470B2 (ja) | 2022-09-06 |
EP3683272A1 (en) | 2020-07-22 |
US20220325102A1 (en) | 2022-10-13 |
US11692098B2 (en) | 2023-07-04 |
EP3683272B1 (en) | 2023-08-16 |
JP2019131827A (ja) | 2019-08-08 |
KR20200041905A (ko) | 2020-04-22 |
EP3683272A4 (en) | 2021-06-09 |
WO2019054109A1 (ja) | 2019-03-21 |
JPWO2019054109A1 (ja) | 2019-11-07 |
KR102580120B1 (ko) | 2023-09-19 |
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