JP2006249445A - 分岐ポリオキシメチレン共重合体の製造方法 - Google Patents
分岐ポリオキシメチレン共重合体の製造方法 Download PDFInfo
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- JP2006249445A JP2006249445A JP2006173464A JP2006173464A JP2006249445A JP 2006249445 A JP2006249445 A JP 2006249445A JP 2006173464 A JP2006173464 A JP 2006173464A JP 2006173464 A JP2006173464 A JP 2006173464A JP 2006249445 A JP2006249445 A JP 2006249445A
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- Prior art keywords
- acid
- polyoxymethylene
- group
- polyoxymethylene copolymer
- ether
- 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.)
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- 229920012196 Polyoxymethylene Copolymer Polymers 0.000 title claims abstract description 71
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 13
- -1 glycidyl compound Chemical class 0.000 claims abstract description 96
- 238000002156 mixing Methods 0.000 claims abstract description 28
- 239000002685 polymerization catalyst Substances 0.000 claims abstract description 24
- 239000000203 mixture Substances 0.000 claims abstract description 23
- 125000004122 cyclic group Chemical group 0.000 claims abstract description 19
- 150000004292 cyclic ethers Chemical class 0.000 claims abstract description 17
- 238000010538 cationic polymerization reaction Methods 0.000 claims abstract description 14
- BGJSXRVXTHVRSN-UHFFFAOYSA-N 1,3,5-trioxane Chemical compound C1OCOCO1 BGJSXRVXTHVRSN-UHFFFAOYSA-N 0.000 claims abstract 4
- YSUQLAYJZDEMOT-UHFFFAOYSA-N 2-(butoxymethyl)oxirane Chemical compound CCCCOCC1CO1 YSUQLAYJZDEMOT-UHFFFAOYSA-N 0.000 claims description 6
- DNVXWIINBUTFEP-UHFFFAOYSA-N 2-[(2-phenylphenoxy)methyl]oxirane Chemical compound C1OC1COC1=CC=CC=C1C1=CC=CC=C1 DNVXWIINBUTFEP-UHFFFAOYSA-N 0.000 claims description 6
- FQYUMYWMJTYZTK-UHFFFAOYSA-N Phenyl glycidyl ether Chemical compound C1OC1COC1=CC=CC=C1 FQYUMYWMJTYZTK-UHFFFAOYSA-N 0.000 claims description 6
- 230000000379 polymerizing effect Effects 0.000 claims description 5
- 238000006116 polymerization reaction Methods 0.000 abstract description 27
- 239000012744 reinforcing agent Substances 0.000 abstract description 6
- 229920006324 polyoxymethylene Polymers 0.000 description 58
- 229930040373 Paraformaldehyde Natural products 0.000 description 46
- 238000000034 method Methods 0.000 description 41
- 239000011342 resin composition Substances 0.000 description 38
- 125000004432 carbon atom Chemical group C* 0.000 description 28
- 239000002253 acid Substances 0.000 description 24
- KQBSGRWMSNFIPG-UHFFFAOYSA-N trioxane Chemical compound C1COOOC1 KQBSGRWMSNFIPG-UHFFFAOYSA-N 0.000 description 23
- 229920000642 polymer Polymers 0.000 description 20
- WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 description 18
- 150000003856 quaternary ammonium compounds Chemical class 0.000 description 18
- 125000000217 alkyl group Chemical group 0.000 description 17
- 239000003795 chemical substances by application Substances 0.000 description 17
- 229910052757 nitrogen Inorganic materials 0.000 description 16
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 15
- 150000001875 compounds Chemical class 0.000 description 15
- 239000000126 substance Substances 0.000 description 15
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 14
- 238000005452 bending Methods 0.000 description 14
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 14
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 14
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 12
- 125000003118 aryl group Chemical group 0.000 description 12
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 12
- 125000005702 oxyalkylene group Chemical group 0.000 description 12
- 238000012360 testing method Methods 0.000 description 12
- 229920009382 Polyoxymethylene Homopolymer Polymers 0.000 description 10
- 239000003054 catalyst Substances 0.000 description 10
- 235000019441 ethanol Nutrition 0.000 description 10
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 10
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 9
- 229910015900 BF3 Inorganic materials 0.000 description 9
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- 238000002347 injection Methods 0.000 description 9
- 239000007924 injection Substances 0.000 description 9
- 125000000547 substituted alkyl group Chemical group 0.000 description 9
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 8
- 229920005989 resin Polymers 0.000 description 8
- 239000011347 resin Substances 0.000 description 8
- WNXJIVFYUVYPPR-UHFFFAOYSA-N 1,3-dioxolane Chemical compound C1COCO1 WNXJIVFYUVYPPR-UHFFFAOYSA-N 0.000 description 7
- 125000001931 aliphatic group Chemical group 0.000 description 7
- 239000003963 antioxidant agent Substances 0.000 description 7
- 239000003484 crystal nucleating agent Substances 0.000 description 7
- 238000001125 extrusion Methods 0.000 description 7
- 238000001746 injection moulding Methods 0.000 description 7
- 239000007788 liquid Substances 0.000 description 7
- TZIHFWKZFHZASV-UHFFFAOYSA-N methyl formate Chemical compound COC=O TZIHFWKZFHZASV-UHFFFAOYSA-N 0.000 description 7
- 150000003839 salts Chemical class 0.000 description 7
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 6
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 6
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 6
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 6
- 239000005062 Polybutadiene Substances 0.000 description 6
- 150000001412 amines Chemical class 0.000 description 6
- 230000003078 antioxidant effect Effects 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 6
- 229920001577 copolymer Polymers 0.000 description 6
- 235000019253 formic acid Nutrition 0.000 description 6
- 239000007789 gas Substances 0.000 description 6
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 6
- 239000000155 melt Substances 0.000 description 6
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 6
- 239000000178 monomer Substances 0.000 description 6
- 238000000465 moulding Methods 0.000 description 6
- 239000002667 nucleating agent Substances 0.000 description 6
- 125000005704 oxymethylene group Chemical group [H]C([H])([*:2])O[*:1] 0.000 description 6
- 229920002857 polybutadiene Polymers 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- 150000007513 acids Chemical class 0.000 description 5
- 125000002947 alkylene group Chemical group 0.000 description 5
- 239000007864 aqueous solution Substances 0.000 description 5
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 5
- 239000004327 boric acid Substances 0.000 description 5
- 150000007942 carboxylates Chemical class 0.000 description 5
- OEYIOHPDSNJKLS-UHFFFAOYSA-N choline Chemical compound C[N+](C)(C)CCO OEYIOHPDSNJKLS-UHFFFAOYSA-N 0.000 description 5
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 5
- 229910052739 hydrogen Inorganic materials 0.000 description 5
- 239000001257 hydrogen Substances 0.000 description 5
- KFZMGEQAYNKOFK-UHFFFAOYSA-N isopropyl alcohol Natural products CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 5
- 239000000049 pigment Substances 0.000 description 5
- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical compound OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 4
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 4
- BDAGIHXWWSANSR-UHFFFAOYSA-M Formate Chemical compound [O-]C=O BDAGIHXWWSANSR-UHFFFAOYSA-M 0.000 description 4
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 4
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 4
- 239000002202 Polyethylene glycol Substances 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- 150000007933 aliphatic carboxylic acids Chemical class 0.000 description 4
- 125000002877 alkyl aryl group Chemical group 0.000 description 4
- 125000003277 amino group Chemical group 0.000 description 4
- 229910021529 ammonia Inorganic materials 0.000 description 4
- 125000003710 aryl alkyl group Chemical group 0.000 description 4
- 229920001400 block copolymer Polymers 0.000 description 4
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 4
- 229910052791 calcium Inorganic materials 0.000 description 4
- 239000011575 calcium Substances 0.000 description 4
- 229910052799 carbon Inorganic materials 0.000 description 4
- 150000001735 carboxylic acids Chemical class 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 229960001231 choline Drugs 0.000 description 4
- 238000001816 cooling Methods 0.000 description 4
- 230000009849 deactivation Effects 0.000 description 4
- GHVNFZFCNZKVNT-UHFFFAOYSA-N decanoic acid Chemical compound CCCCCCCCCC(O)=O GHVNFZFCNZKVNT-UHFFFAOYSA-N 0.000 description 4
- NKDDWNXOKDWJAK-UHFFFAOYSA-N dimethoxymethane Chemical compound COCOC NKDDWNXOKDWJAK-UHFFFAOYSA-N 0.000 description 4
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 4
- 125000005843 halogen group Chemical group 0.000 description 4
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 4
- 239000003921 oil Substances 0.000 description 4
- 150000007524 organic acids Chemical class 0.000 description 4
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 4
- 230000000704 physical effect Effects 0.000 description 4
- 229920001223 polyethylene glycol Polymers 0.000 description 4
- 239000012779 reinforcing material Substances 0.000 description 4
- 150000005846 sugar alcohols Polymers 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- AUAGGMPIKOZAJZ-UHFFFAOYSA-N 1,3,6-trioxocane Chemical compound C1COCOCCO1 AUAGGMPIKOZAJZ-UHFFFAOYSA-N 0.000 description 3
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 3
- 239000002841 Lewis acid Substances 0.000 description 3
- 229920002292 Nylon 6 Polymers 0.000 description 3
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 3
- 239000006096 absorbing agent Substances 0.000 description 3
- 235000011054 acetic acid Nutrition 0.000 description 3
- NJYZCEFQAIUHSD-UHFFFAOYSA-N acetoguanamine Chemical compound CC1=NC(N)=NC(N)=N1 NJYZCEFQAIUHSD-UHFFFAOYSA-N 0.000 description 3
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 3
- 150000008065 acid anhydrides Chemical class 0.000 description 3
- 150000001298 alcohols Chemical class 0.000 description 3
- 150000008064 anhydrides Chemical class 0.000 description 3
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 3
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 3
- 238000000354 decomposition reaction Methods 0.000 description 3
- 229920001971 elastomer Polymers 0.000 description 3
- 239000000806 elastomer Substances 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 3
- 150000007517 lewis acids Chemical class 0.000 description 3
- 239000004611 light stabiliser Substances 0.000 description 3
- 239000000314 lubricant Substances 0.000 description 3
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- BDERNNFJNOPAEC-UHFFFAOYSA-N n-propyl alcohol Natural products CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 3
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- FCKXGFANXSHGAW-DTXPUJKBSA-N (2s)-n,n'-bis[(2s)-1-(2-chloro-4-nitroanilino)-1-oxo-3-phenylpropan-2-yl]-2-hydroxybutanediamide Chemical compound C([C@H](NC(=O)C[C@H](O)C(=O)N[C@@H](CC=1C=CC=CC=1)C(=O)NC=1C(=CC(=CC=1)[N+]([O-])=O)Cl)C(=O)NC=1C(=CC(=CC=1)[N+]([O-])=O)Cl)C1=CC=CC=C1 FCKXGFANXSHGAW-DTXPUJKBSA-N 0.000 description 2
- NWHNXXMYEICZAT-UHFFFAOYSA-N 1,2,2,6,6-pentamethylpiperidin-4-ol Chemical compound CN1C(C)(C)CC(O)CC1(C)C NWHNXXMYEICZAT-UHFFFAOYSA-N 0.000 description 2
- FQERLIOIVXPZKH-UHFFFAOYSA-N 1,2,4-trioxane Chemical compound C1COOCO1 FQERLIOIVXPZKH-UHFFFAOYSA-N 0.000 description 2
- ULAGGPJVDRGWTI-UHFFFAOYSA-N 1,3,5-trioxepane Chemical compound C1COCOCO1 ULAGGPJVDRGWTI-UHFFFAOYSA-N 0.000 description 2
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- QUFMVAWAOYDYFV-UHFFFAOYSA-N 10-hydroxyhexadecanoic acid Chemical compound CCCCCCC(O)CCCCCCCCC(O)=O QUFMVAWAOYDYFV-UHFFFAOYSA-N 0.000 description 2
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- ULQISTXYYBZJSJ-UHFFFAOYSA-N 12-hydroxyoctadecanoic acid Chemical compound CCCCCCC(O)CCCCCCCCCCC(O)=O ULQISTXYYBZJSJ-UHFFFAOYSA-N 0.000 description 2
- UGAGPNKCDRTDHP-UHFFFAOYSA-N 16-hydroxyhexadecanoic acid Chemical compound OCCCCCCCCCCCCCCCC(O)=O UGAGPNKCDRTDHP-UHFFFAOYSA-N 0.000 description 2
- ZMWRRFHBXARRRT-UHFFFAOYSA-N 2-(benzotriazol-2-yl)-4,6-bis(2-methylbutan-2-yl)phenol Chemical compound CCC(C)(C)C1=CC(C(C)(C)CC)=CC(N2N=C3C=CC=CC3=N2)=C1O ZMWRRFHBXARRRT-UHFFFAOYSA-N 0.000 description 2
- LHPPDQUVECZQSW-UHFFFAOYSA-N 2-(benzotriazol-2-yl)-4,6-ditert-butylphenol Chemical compound CC(C)(C)C1=CC(C(C)(C)C)=CC(N2N=C3C=CC=CC3=N2)=C1O LHPPDQUVECZQSW-UHFFFAOYSA-N 0.000 description 2
- HJEORQYOUWYAMR-UHFFFAOYSA-N 2-[(2-butylphenoxy)methyl]oxirane Chemical group CCCCC1=CC=CC=C1OCC1OC1 HJEORQYOUWYAMR-UHFFFAOYSA-N 0.000 description 2
- SYEWHONLFGZGLK-UHFFFAOYSA-N 2-[1,3-bis(oxiran-2-ylmethoxy)propan-2-yloxymethyl]oxirane Chemical compound C1OC1COCC(OCC1OC1)COCC1CO1 SYEWHONLFGZGLK-UHFFFAOYSA-N 0.000 description 2
- SEFYJVFBMNOLBK-UHFFFAOYSA-N 2-[2-[2-(oxiran-2-ylmethoxy)ethoxy]ethoxymethyl]oxirane Chemical compound C1OC1COCCOCCOCC1CO1 SEFYJVFBMNOLBK-UHFFFAOYSA-N 0.000 description 2
- QSRJVOOOWGXUDY-UHFFFAOYSA-N 2-[2-[2-[3-(3-tert-butyl-4-hydroxy-5-methylphenyl)propanoyloxy]ethoxy]ethoxy]ethyl 3-(3-tert-butyl-4-hydroxy-5-methylphenyl)propanoate Chemical compound CC(C)(C)C1=C(O)C(C)=CC(CCC(=O)OCCOCCOCCOC(=O)CCC=2C=C(C(O)=C(C)C=2)C(C)(C)C)=C1 QSRJVOOOWGXUDY-UHFFFAOYSA-N 0.000 description 2
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- PQJZHMCWDKOPQG-UHFFFAOYSA-N 2-anilino-2-oxoacetic acid Chemical compound OC(=O)C(=O)NC1=CC=CC=C1 PQJZHMCWDKOPQG-UHFFFAOYSA-N 0.000 description 2
- RLHGFJMGWQXPBW-UHFFFAOYSA-N 2-hydroxy-3-(1h-imidazol-5-ylmethyl)benzamide Chemical compound NC(=O)C1=CC=CC(CC=2NC=NC=2)=C1O RLHGFJMGWQXPBW-UHFFFAOYSA-N 0.000 description 2
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- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 2
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- MECNWXGGNCJFQJ-UHFFFAOYSA-N 3-piperidin-1-ylpropane-1,2-diol Chemical compound OCC(O)CN1CCCCC1 MECNWXGGNCJFQJ-UHFFFAOYSA-N 0.000 description 2
- GZVHEAJQGPRDLQ-UHFFFAOYSA-N 6-phenyl-1,3,5-triazine-2,4-diamine Chemical compound NC1=NC(N)=NC(C=2C=CC=CC=2)=N1 GZVHEAJQGPRDLQ-UHFFFAOYSA-N 0.000 description 2
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- 229920000049 Carbon (fiber) Polymers 0.000 description 2
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- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 2
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- ADXGNEYLLLSOAR-UHFFFAOYSA-N tasosartan Chemical compound C12=NC(C)=NC(C)=C2CCC(=O)N1CC(C=C1)=CC=C1C1=CC=CC=C1C=1N=NNN=1 ADXGNEYLLLSOAR-UHFFFAOYSA-N 0.000 description 1
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- DZLFLBLQUQXARW-UHFFFAOYSA-N tetrabutylammonium Chemical compound CCCC[N+](CCCC)(CCCC)CCCC DZLFLBLQUQXARW-UHFFFAOYSA-N 0.000 description 1
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- 125000002889 tridecyl 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])[H] 0.000 description 1
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- 125000002948 undecyl 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])[H] 0.000 description 1
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Landscapes
- Polyoxymethylene Polymers And Polymers With Carbon-To-Carbon Bonds (AREA)
Abstract
【解決手段】 トリオキサン(a)、単官能グリシジル化合物(b)、環状エーテル及び/又は環状ホルマール(c)をカチオン重合触媒を用いて共重合するに際し、単管能グリシジル化合物(b)と環状エーテル及び/又は環状ホルマール(c)及びトリオキサン(a)をあらかじめ混合した混合物にカチオン重合触媒を添加して重合することを特徴とする分岐ポリオキシメチレン共重合体の製造方法。
【選択図】なし
Description
即ち本発明は、1.トリオキサン(a)、単官能グリシジル化合物(b)、環状エーテル及び/又は環状ホルマール(c)をカチオン重合触媒を用いて共重合するに際し、単官能グリシジル化合物(b)と環状エーテル及び/又は環状ホルマール(c)及びトリオキサン(a)をあらかじめ混合した混合物にカチオン重合触媒を添加して重合することを特徴とする分岐ポリオキシメチレン共重合体の製造方法、
2.単官能グリシジル化合物(b)がブチルグリシジルエーテル、フェニルグリシジルエーテル、フェニルフェノールグリシジルエーテルより選ばれる少なくとも1種であることを特徴とする1記載の分岐ポリオキシメチレン共重合体の製造方法、
その他、本発明は以下の態様も包含している。
3.単官能グリシジルエーテルが下記一般式(2)、(3)、(4)で表される前記2.に記載の分岐ポリオキシメチレン共重合体の製造方法。
5.該分岐ポリオキシメチレン共重合体が下記に示すポリオキシメチレン共重合体の有する不安定な末端部の分解除去処理を経て得られたものであることを特徴とする前記1.〜4.のいずれかに記載の分岐ポリオキシメチレン共重合体の製造方法。
[R1R2R3R4N+]nX-n(5)
(式中、Pは第4級アンモニウム化合物のポリオキシメチレン共重合体及び第4級アンモニウム化合物の合計重量に対する量(ppm)を表わし、14は窒素の原子量であり、Qは第4級アンモニウム化合物の分子量を表わす。)
本発明の方法により得られる共重合体は、オキシメチレン単位(−CH2O−)と、下記一般式(1)に示されたオキシアルキレン単位から構成される分岐を有するポリオキシメチレン共重合体において、一般式(1)のn=1の割合がオキシアルキレン単位全体の95mol%以上、n≧2の割合がオキシアルキレン単位全体の5mol%未満である分岐ポリオキシメチレン共重合体である。
重合時の水素添加液状ポリブタジエン添加時期は、重合反応が開始される前であれば特に制限はなく、予めトリオキサンや単官能グリシジルエーテル、環状エーテル及び/又は環状ホルマール、又はそれらの混合物に添加しておくことも可能であるし、トリオキサンや単官能グリシジルエーテル、環状エーテル及び/又は環状ホルマールを重合装置にフィードする際に、別途フィードすることも可能である。本発明において、トリオキサン(a)100質量部に対し両末端をヒドロキシアルキル化された水素添加液状ポリブタジエン(d)は熱安定性確保の点から0.001〜10質量部を混合して重合することが好ましい。より好ましくは5質量部以下である。
(式中、 R1 、R2 、R3 、R4は、各々独立して、炭素数1〜30の非置換アルキル基または置換アルキル基;炭素数6〜20のアリール基;炭素数1〜30の非置換アルキル基または置換アルキル基が少なくとも1個の炭素数6〜20のアリール基で置換されたアラルキル基;または炭素数6〜20のアリール基が少なくとも1個の炭素数1〜30の非置換アルキル基または置換アルキル基で置換されたアルキルアリール基を表わし、非置換アルキル基または置換アルキル基は直鎖状、分岐状、または環状である。上記置換アルキル基の置換基はハロゲン、水酸基、アルデヒド基、カルボキシル基、アミノ基、またはアミド基である。また、上記非置換アルキル基、アリール基、アラルキル基、アルキルアリール基は水素原子がハロゲンで置換されていてもよい。nは1〜3の整数を表わす。Xは水酸基、または炭素数1〜20のカルボン酸、ハロゲン化水素以外の水素酸、オキソ酸、無機チオ酸もしくは炭素数1〜20の有機チオ酸の酸残基を表す。)
P×14/Q (6)
(式中、Pは第4級アンモニウム化合物のポリオキシメチレン共重合体及び第4級アンモニウム化合物の合計質量に対する量(ppm)を表わし、14は窒素の原子量であり、Qは第4級アンモニウム化合物の分子量を表わす。)
R10COOCOR11 (8)
(式中、R10、R11は、各々、独立にアルキル基を示す。R10、R11は、同じであっても異なっていてもよい。)
<シークエンス>重合体100gを0.1規定塩酸水溶液300mlと混合して耐圧ビンに仕込み、それを滅菌器により加圧状態で120℃、2時間分解させ、ガスクロマトグラフィーを用いて、オキシアルキレングリコールの定量を行い、シークエンスn=1及びn≧2の量をmol%で示した。
<曲げ試験>東芝(株)製IS−80A射出成形機を用い、シリンダー温度200℃、射出圧力60kgf/cm2、射出時間15秒、冷却時間25秒、金型温度70℃にて試験片を作製し、ASTMD790に基づき測定した。
<IZOD衝撃強さ(J/m)>東芝(株)製IS−80A射出成形機を用い、シリンダー温度200℃、射出圧力5.9MPa、射出時間15秒、冷却時間25秒、金型温度70℃にて試験片を作製し、ASTMD256に基づき、温度23℃、ノッチ有りにて測定した。
<二次収縮率(%)>曲げ弾性率測定用試験片作製と全く同じ射出成形機、射出条件で試験片を作製した。成形完了後、23℃、湿度50%の環境下に48時間放置した後の流動方向の寸法をD1(mm)とし、成形完了後、23℃、湿度50%の環境下に72時間放置した後、120℃で24時間加熱し、その後23℃で48時間放置した後の流動方向の寸法をD2(mm)として、次式に従い二次収縮率を(%)を求めた。
二次収縮率(%)={(D1−D2)/金型寸法}×100ただし、金型寸法は130mm、厚さは3mmで、値が小さい程二次収縮性に優れる。
<%、ppm>特に断らない限り、全て質量基準である。
熱媒を通すことができるジャケット付きの2軸パドル型連続重合機(スクリュー径3インチ、L/D=10)を80℃に調整し、スタティックミキサーを設置した配管を用いて表1に示すような量のモノマーであるトリオキサン(a)、コモノマーである1,3−ジオキソラン(c)、ブチルグリシジルエーテル(b―1)、フェニルグリシジルエーテル(b―2)またはフェニルフェノールグリシジルエーテル(b―3)と、分子量調節剤として純度98%、ギ酸メチル含有量が1.1%のメチラールを混合して連続的に添加した。さらに、重合触媒として、三フッ化ホウ素が、トリオキサン1モルに対して1.5×10-5モルになるように、三フッ化ホウ素ジ−n−ブチルエーテラート1wt%のシクロヘキサン溶液を連続的に添加し重合を行った。連続重合機から排出された分岐ポリオキシメチレン共重合体をトリエチルアミン0.1%水溶液中に投入し重合触媒の失活を行った。失活された分岐ポリオキシメチレン共重合体を遠心分離機でろ過した。ここでの粗収率は86%であった。ろ過後の分岐ポリオキシメチレン共重合体100質量部に対して、第4級アンモニウム化合物として水酸化コリン蟻酸塩(トリメチル−2−ヒドロキシエチルアンモニウムフォルメート)を含有した水溶液1質量部を添加して、均一に混合した後120℃で乾燥した。水酸化コリン蟻酸塩の添加量は窒素の量に換算して20ppmとした。水酸化コリン蟻酸塩の添加量は、添加する水酸化コリン蟻酸塩を含有した水溶液中の水酸化コリン蟻酸塩の濃度を調整することにより行った。この乾燥後のパウダー状の分岐ポリオキシメチレン共重合体100質量部に対して、酸化防止剤として、2,2’−メチレンビス−(4−メチル−t−ブチルフェノール)を0.3質量部添加し、ベント付き2軸スクリュー式押出機に供給した。押出機中の溶融しているポリオキシメチレン共重合体100質量部に対して水0.5質量部添加し、押出機設定温度200℃、押出機における滞留時間5分でベント真空度20Torrの条件下に脱揮しながら不安定末端部の分解を行った。押出機ダイス部よりストランドとして排出されたポリオキシメチレン樹脂組成物を、冷水浴中にて冷却した後、ストランドカッターを用いてペレット化した。得られたポリオキシメチレン樹脂組成物を80℃で3時間乾燥した後、シークエンス、MIを測定し、更に成形片の曲げ強度、引っ張り強度、Izod衝撃値、耐クリープ特性、熱安定性を測定した。また実施例2について重合、押出時の電流負荷を観察した。結果を表1、2、3に示した。
コモノマーである1,3−ジオキソラン(c)を導入しない以外は実施例2、3と同様な方法で分岐ポリオキシメチレン共重合体を製造し、ペレット状のポリオキシメチレン樹脂組成物を得た。得られたポリオキシメチレン樹脂組成物を80℃で3時間乾燥した後、シークエンス、MIを測定し、更に成形片の曲げ強度、引っ張り強度、Izod衝撃値、耐クリープ特性、熱安定性を測定した。結果を表1、2に示した。
実施例2、3、10、13と同様にして、重合、触媒の失活、水酸化コリン蟻酸塩を添加後に乾燥を行ったパウダー状の分岐ポリオキシメチレン共重合体と、グリシジル化合物を導入しない以外は実施例1〜14と同様な方法で製造したパウダー状の線状ポリオキシメチレン重合体または旭化成(株)製「TENAC−2010」または「TENAC−C3510」を表1の様な混合比で混合し、実施例1〜14と同様な方法でペレット状のポリオキシメチレン樹脂組成物を得た。得られたポリオキシメチレン樹脂組成物を80℃で3時間乾燥した後、シークエンス、MIを測定し、更に成形片の曲げ強度、引っ張り強度、Izod衝撃値、耐クリープ特性、熱安定性を測定した。結果を表1、2に示した。
コモノマーである1,3−ジオキソラン(c)を混合しない以外は実施例2と同様な方法で製造した分岐ポリオキシメチレン共重合体とグリシジル化合物を導入しない以外は実施例2、3と同様な方法で製造したパウダー状の線状ポリオキシメチレン重合体を表1の様な混合比で混合し、実施例1〜14と同様な方法でペレット状のポリオキシメチレン樹脂組成物を得た。得られたポリオキシメチレン樹脂組成物を80℃で3時間乾燥した後、シークエンス、MIを測定し、更に成形片の曲げ強度、引っ張り強度、Izod衝撃値、耐クリープ特性、熱安定性を測定した。結果を表1、2に示した。
実施例2と同様な重合機を用いて、スタティックミキサーを設置した配管にナトリウムを触媒としてブタジエンを重合しエチレンオキシドで両末端をヒドロキシアルキル化され次いで水素添加処理された両末端ヒドロキシエチル化された23℃、1気圧で液状の水素添加ポリブタジエン(1,2結合を80モル%、1,4結合を20モル%、1,4結合は1,2結合に対しランダムに存在する。以降断らない限り1,4結合と1,2結合はランダムに存在するものとする。数平均分子量2,390、ヨウ素価18g−I2/100g、Mw/Mn=1.5)(d)を更に添加する以外は実施例2と同様な方法でペレットを得た。得られたポリオキシメチレン樹脂組成物を80℃で3時間乾燥した後、シークエンス、MIを測定し、更に成形片の曲げ強度、引っ張り強度、Izod衝撃値、耐クリープ特性、熱安定性を測定した。また重合、押出時の電流負荷を観察した。結果を表1、2、3に示した。
実施例2と同様な方法でパウダー状の分岐ポリオキシメチレン共重合体を製造し、実施例2と同様な酸化防止剤と表1に示される結晶核剤(E−1またはE−2)を配合し、実施例2と同様な方法でペレット状のポリオキシメチレン樹脂組成物を得た。得られたポリオキシメチレン樹脂組成物を80℃で3時間乾燥した後、シークエンス、MIを測定し、更に成形片の曲げ強度、引っ張り強度、Izod衝撃値、耐クリープ特性、熱安定性を測定した。結果を表1、2に示した。
実施例31と同様な方法で得られたパウダー状の分岐ポリオキシメチレン共重合体と実施例2と同様な酸化防止剤と表1に示される結晶核剤(E−1)を配合し、実施例2と同様な方法でペレット状のポリオキシメチレン樹脂組成物を得た。得られたポリオキシメチレン樹脂組成物を80℃で3時間乾燥した後、シークエンス、MIを測定し、更に成形片の曲げ強度、引っ張り強度、Izod衝撃値、耐クリープ特性、熱安定性を測定した。結果を表1、2に示した。
実施例31と同様な方法で製造したパウダー状の分岐ポリオキシメチレン共重合体にグリシジルエーテルを導入しない以外は実施例3と同様な方法で製造したパウダー状の線状ポリオキシメチレン重合体及び/または表1で示される結晶核剤を配合し、実施例1〜14と同様な方法でペレット状のポリオキシメチレン樹脂組成物を得た。得られたポリオキシメチレン樹脂組成物を80℃で3時間乾燥した後、シークエンス、MIを測定し、更に成形片の曲げ強度、引っ張り強度、Izod衝撃値、耐クリープ特性、熱安定性を測定した。結果を表1、2に示した。
実施例2と同様な方法で製造したパウダー状の分岐ポリオキシメチレン共重合体とグリシジルエーテルを導入しない以外は実施例3と同様な方法で製造したパウダー状の線状ポリオキシメチレン重合体及び表1で示される結晶核剤(E−1)を配合し、実施例1〜14と同様な方法でペレット状のポリオキシメチレン樹脂組成物を得た。得られたポリオキシメチレン樹脂組成物を80℃で3時間乾燥した後、シークエンス、MIを測定し、更に成形片の曲げ強度、引っ張り強度、Izod衝撃値、耐クリープ特性、熱安定性を測定した。結果を表1、2に示した。
グリシジルエーテルを導入しない以外は実施例1〜3と同様な方法でペレット状の線状ポリオキシメチレン重合体を得た。得られたポリオキシメチレン樹脂組成物を80℃で3時間乾燥した後、シークエンス、MIを測定し、更に成形片の曲げ強度、引っ張り強度、Izod衝撃値、耐クリープ特性、熱安定性を測定した。結果を表1、2に示した。
熱媒を通すことができるジャケット付きの2軸パドル型連続重合機(スクリュー径3インチ、L/D=10)を80℃に調整し、表1に示すような量のモノマーであるトリオキサン、コモノマーである1,3−ジオキソラン、ブチルグリシジルエーテルと、分子量調節剤として純度98%、ギ酸メチル含有量が1.1%のメチラールをそれぞれ単独に連続的に添加した。さらに、重合触媒として、三フッ化ホウ素が、トリオキサン1モルに対して1.5×10-5モルになるように、三フッ化ホウ素ジ−n−ブチルエーテラート1wt%のシクロヘキサン溶液を連続的に添加し重合を行った。得られた分岐ポリオキシメチレンを実施例1と同様な方法でペレット状のポリオキシメチレン樹脂組成物とした。得られたポリオキシメチレン樹脂組成物を80℃で3時間乾燥した後、シークエンス、MIを測定し、更に成形片の曲げ強度、引っ張り強度、Izod衝撃値、耐クリープ特性、熱安定性を測定した。結果を表1、2に示した。
コモノマーである1,3−ジオキソランを導入しない以外は比較例4と同様な方法で分岐ポリオキシメチレン共重合体を製造し、ペレット状のポリオキシメチレン樹脂組成物を得た。得られたポリオキシメチレン樹脂組成物を80℃で3時間乾燥した後、シークエンス、MIを測定し、更に成形片の曲げ強度、引っ張り強度、Izod衝撃値、耐クリープ特性、熱安定性を測定した。結果を表1、2に示した。
「TENAC−2010」、「TENAC−C3510」ペレットを80℃で3時間乾燥した後、シークエンス、MIを測定し、更に成形片の曲げ強度、引っ張り強度、Izod衝撃値、耐クリープ特性、熱安定性を測定した。結果を表1、2に示した。
Claims (2)
- トリオキサン(a)、単官能グリシジル化合物(b)、環状エーテル及び/又は環状ホルマール(c)をカチオン重合触媒を用いて共重合するに際し、単管能グリシジル化合物(b)と環状エーテル及び/又は環状ホルマール(c)及びトリオキサン(a)をあらかじめ混合した混合物にカチオン重合触媒を添加して重合することを特徴とする分岐ポリオキシメチレン共重合体の製造方法。
- 単官能グリシジル化合物(b)がブチルグリシジルエーテル、フェニルグリシジルエーテル、フェニルフェノールグリシジルエーテルより選ばれる少なくとも1種であることを特徴とする請求項1記載の分岐ポリオキシメチレン共重合体の製造方法。
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WO2008032686A1 (fr) | 2006-09-14 | 2008-03-20 | Cosmo Oil Co., Ltd. | Catalyseur d'hydrodésulfuration/déparaffinage pour un hydrocarbure liquide, procédé servant à produire celui-ci et procédé d'hydrotraitement d'un hydrocarbure liquide avec le catalyseur |
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JP2013001710A (ja) * | 2011-06-10 | 2013-01-07 | Asahi Kasei Chemicals Corp | ポリアセタールブロックコポリマー |
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Publication number | Priority date | Publication date | Assignee | Title |
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WO2008032686A1 (fr) | 2006-09-14 | 2008-03-20 | Cosmo Oil Co., Ltd. | Catalyseur d'hydrodésulfuration/déparaffinage pour un hydrocarbure liquide, procédé servant à produire celui-ci et procédé d'hydrotraitement d'un hydrocarbure liquide avec le catalyseur |
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JP2011116907A (ja) * | 2009-12-06 | 2011-06-16 | Mitsubishi Gas Chemical Co Inc | ポリアセタール樹脂組成物 |
JP2013001710A (ja) * | 2011-06-10 | 2013-01-07 | Asahi Kasei Chemicals Corp | ポリアセタールブロックコポリマー |
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