JP2020500962A - 有機亜鉛触媒の製造方法と前記方法で製造された有機亜鉛触媒、および前記触媒を用いたポリアルキレンカーボネート樹脂の製造方法 - Google Patents
有機亜鉛触媒の製造方法と前記方法で製造された有機亜鉛触媒、および前記触媒を用いたポリアルキレンカーボネート樹脂の製造方法 Download PDFInfo
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- JP2020500962A JP2020500962A JP2019526250A JP2019526250A JP2020500962A JP 2020500962 A JP2020500962 A JP 2020500962A JP 2019526250 A JP2019526250 A JP 2019526250A JP 2019526250 A JP2019526250 A JP 2019526250A JP 2020500962 A JP2020500962 A JP 2020500962A
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- Prior art keywords
- zirconium
- zinc
- catalyst
- acid
- producing
- Prior art date
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- 239000003054 catalyst Substances 0.000 title claims abstract description 113
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 title claims abstract description 33
- 239000011347 resin Substances 0.000 title claims abstract description 33
- 229920005989 resin Polymers 0.000 title claims abstract description 33
- 229920001281 polyalkylene Polymers 0.000 title claims abstract description 32
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 29
- 238000000034 method Methods 0.000 title claims abstract description 23
- 239000011701 zinc Substances 0.000 claims abstract description 89
- 229910052725 zinc Inorganic materials 0.000 claims abstract description 80
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims abstract description 75
- 230000002194 synthesizing effect Effects 0.000 claims abstract 3
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 claims description 58
- 229910052726 zirconium Inorganic materials 0.000 claims description 58
- 239000002243 precursor Substances 0.000 claims description 40
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 36
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 33
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 claims description 26
- 150000001875 compounds Chemical class 0.000 claims description 24
- 239000002904 solvent Substances 0.000 claims description 24
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 claims description 22
- 238000006243 chemical reaction Methods 0.000 claims description 19
- 125000004432 carbon atom Chemical group C* 0.000 claims description 16
- 239000003426 co-catalyst Substances 0.000 claims description 16
- 150000002118 epoxides Chemical class 0.000 claims description 15
- 239000012621 metal-organic framework Substances 0.000 claims description 14
- RTBFRGCFXZNCOE-UHFFFAOYSA-N 1-methylsulfonylpiperidin-4-one Chemical compound CS(=O)(=O)N1CCC(=O)CC1 RTBFRGCFXZNCOE-UHFFFAOYSA-N 0.000 claims description 13
- JFCQEDHGNNZCLN-UHFFFAOYSA-N anhydrous glutaric acid Natural products OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 claims description 13
- 239000013207 UiO-66 Substances 0.000 claims description 11
- 239000001569 carbon dioxide Substances 0.000 claims description 11
- 229910002092 carbon dioxide Inorganic materials 0.000 claims description 11
- DUNKXUFBGCUVQW-UHFFFAOYSA-J zirconium tetrachloride Chemical compound Cl[Zr](Cl)(Cl)Cl DUNKXUFBGCUVQW-UHFFFAOYSA-J 0.000 claims description 10
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 claims description 9
- 229910052751 metal Inorganic materials 0.000 claims description 9
- 239000002184 metal Substances 0.000 claims description 9
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 claims description 9
- ZHQLTKAVLJKSKR-UHFFFAOYSA-N homophthalic acid Chemical compound OC(=O)CC1=CC=CC=C1C(O)=O ZHQLTKAVLJKSKR-UHFFFAOYSA-N 0.000 claims description 7
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 6
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 claims description 6
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 claims description 6
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 claims description 6
- 239000000178 monomer Substances 0.000 claims description 5
- CGWDABYOHPEOAD-VIFPVBQESA-N (2r)-2-[(4-fluorophenoxy)methyl]oxirane Chemical compound C1=CC(F)=CC=C1OC[C@@H]1OC1 CGWDABYOHPEOAD-VIFPVBQESA-N 0.000 claims description 4
- DUFCMRCMPHIFTR-UHFFFAOYSA-N 5-(dimethylsulfamoyl)-2-methylfuran-3-carboxylic acid Chemical compound CN(C)S(=O)(=O)C1=CC(C(O)=O)=C(C)O1 DUFCMRCMPHIFTR-UHFFFAOYSA-N 0.000 claims description 4
- 239000013208 UiO-67 Substances 0.000 claims description 4
- BSDOQSMQCZQLDV-UHFFFAOYSA-N butan-1-olate;zirconium(4+) Chemical compound [Zr+4].CCCC[O-].CCCC[O-].CCCC[O-].CCCC[O-] BSDOQSMQCZQLDV-UHFFFAOYSA-N 0.000 claims description 4
- XPGAWFIWCWKDDL-UHFFFAOYSA-N propan-1-olate;zirconium(4+) Chemical compound [Zr+4].CCC[O-].CCC[O-].CCC[O-].CCC[O-] XPGAWFIWCWKDDL-UHFFFAOYSA-N 0.000 claims description 4
- KASZLOODWXOZIF-UHFFFAOYSA-N terephthalic acid;zirconium Chemical compound [Zr].OC(=O)C1=CC=C(C(O)=O)C=C1 KASZLOODWXOZIF-UHFFFAOYSA-N 0.000 claims description 4
- OMQSJNWFFJOIMO-UHFFFAOYSA-J zirconium tetrafluoride Chemical compound F[Zr](F)(F)F OMQSJNWFFJOIMO-UHFFFAOYSA-J 0.000 claims description 4
- YOBOXHGSEJBUPB-MTOQALJVSA-N (z)-4-hydroxypent-3-en-2-one;zirconium Chemical compound [Zr].C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O YOBOXHGSEJBUPB-MTOQALJVSA-N 0.000 claims description 3
- GOEBEEJCYYXSFT-UHFFFAOYSA-N 2-phenylpentanedioic acid Chemical compound OC(=O)CCC(C(O)=O)C1=CC=CC=C1 GOEBEEJCYYXSFT-UHFFFAOYSA-N 0.000 claims description 3
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 claims description 3
- ZOIORXHNWRGPMV-UHFFFAOYSA-N acetic acid;zinc Chemical compound [Zn].CC(O)=O.CC(O)=O ZOIORXHNWRGPMV-UHFFFAOYSA-N 0.000 claims description 3
- 239000001361 adipic acid Substances 0.000 claims description 3
- 235000011037 adipic acid Nutrition 0.000 claims description 3
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 claims description 3
- 230000000379 polymerizing effect Effects 0.000 claims description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 3
- 239000004246 zinc acetate Substances 0.000 claims description 3
- GTQFPPIXGLYKCZ-UHFFFAOYSA-L zinc chlorate Chemical compound [Zn+2].[O-]Cl(=O)=O.[O-]Cl(=O)=O GTQFPPIXGLYKCZ-UHFFFAOYSA-L 0.000 claims description 3
- UGZADUVQMDAIAO-UHFFFAOYSA-L zinc hydroxide Chemical compound [OH-].[OH-].[Zn+2] UGZADUVQMDAIAO-UHFFFAOYSA-L 0.000 claims description 3
- 229940007718 zinc hydroxide Drugs 0.000 claims description 3
- 229910021511 zinc hydroxide Inorganic materials 0.000 claims description 3
- ONDPHDOFVYQSGI-UHFFFAOYSA-N zinc nitrate Chemical compound [Zn+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O ONDPHDOFVYQSGI-UHFFFAOYSA-N 0.000 claims description 3
- NWONKYPBYAMBJT-UHFFFAOYSA-L zinc sulfate Chemical compound [Zn+2].[O-]S([O-])(=O)=O NWONKYPBYAMBJT-UHFFFAOYSA-L 0.000 claims description 3
- 229960001763 zinc sulfate Drugs 0.000 claims description 3
- 229910000368 zinc sulfate Inorganic materials 0.000 claims description 3
- 239000007795 chemical reaction product Substances 0.000 claims description 2
- 239000011368 organic material Substances 0.000 claims 1
- 238000006116 polymerization reaction Methods 0.000 abstract description 17
- 230000003197 catalytic effect Effects 0.000 abstract description 9
- 230000008569 process Effects 0.000 abstract description 3
- 239000007787 solid Substances 0.000 description 17
- 230000000694 effects Effects 0.000 description 16
- 239000000203 mixture Substances 0.000 description 14
- 239000002245 particle Substances 0.000 description 13
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 12
- 239000011787 zinc oxide Substances 0.000 description 12
- 238000010438 heat treatment Methods 0.000 description 11
- 238000010992 reflux Methods 0.000 description 9
- 229940008309 acetone / ethanol Drugs 0.000 description 8
- 239000011259 mixed solution Substances 0.000 description 8
- SCRKTTJILRGIEY-UHFFFAOYSA-N pentanedioic acid;zinc Chemical compound [Zn].OC(=O)CCCC(O)=O SCRKTTJILRGIEY-UHFFFAOYSA-N 0.000 description 8
- 230000000052 comparative effect Effects 0.000 description 7
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 7
- -1 glutaric acid Chemical compound 0.000 description 7
- 238000003786 synthesis reaction Methods 0.000 description 7
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 5
- QPFMBZIOSGYJDE-UHFFFAOYSA-N 1,1,2,2-tetrachloroethane Chemical compound ClC(Cl)C(Cl)Cl QPFMBZIOSGYJDE-UHFFFAOYSA-N 0.000 description 4
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 4
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 4
- 125000000217 alkyl group Chemical group 0.000 description 4
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- 230000008901 benefit Effects 0.000 description 3
- 229910052736 halogen Inorganic materials 0.000 description 3
- 150000002367 halogens Chemical group 0.000 description 3
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- 150000003624 transition metals Chemical class 0.000 description 3
- UOCLXMDMGBRAIB-UHFFFAOYSA-N 1,1,1-trichloroethane Chemical compound CC(Cl)(Cl)Cl UOCLXMDMGBRAIB-UHFFFAOYSA-N 0.000 description 2
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- HFDVRLIODXPAHB-UHFFFAOYSA-N 1-tetradecene Chemical compound CCCCCCCCCCCCC=C HFDVRLIODXPAHB-UHFFFAOYSA-N 0.000 description 2
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- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 2
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- 239000006227 byproduct Substances 0.000 description 2
- 229910017052 cobalt Inorganic materials 0.000 description 2
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- 239000003125 aqueous solvent Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- FGYBPGJIUUUVTL-UHFFFAOYSA-N benzene-1,3-dicarboxylic acid;zinc Chemical compound [Zn].OC(=O)C1=CC=CC(C(O)=O)=C1 FGYBPGJIUUUVTL-UHFFFAOYSA-N 0.000 description 1
- 229930188620 butyrolactone Natural products 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 229910000428 cobalt oxide Inorganic materials 0.000 description 1
- IVMYJDGYRUAWML-UHFFFAOYSA-N cobalt(ii) oxide Chemical compound [Co]=O IVMYJDGYRUAWML-UHFFFAOYSA-N 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 125000002993 cycloalkylene group Chemical group 0.000 description 1
- ZWAJLVLEBYIOTI-UHFFFAOYSA-N cyclohexene oxide Chemical compound C1CCCC2OC21 ZWAJLVLEBYIOTI-UHFFFAOYSA-N 0.000 description 1
- FWFSEYBSWVRWGL-UHFFFAOYSA-N cyclohexene oxide Natural products O=C1CCCC=C1 FWFSEYBSWVRWGL-UHFFFAOYSA-N 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- DFBKLUNHFCTMDC-PICURKEMSA-N dieldrin Chemical compound C([C@H]1[C@H]2[C@@]3(Cl)C(Cl)=C([C@]([C@H]22)(Cl)C3(Cl)Cl)Cl)[C@H]2[C@@H]2[C@H]1O2 DFBKLUNHFCTMDC-PICURKEMSA-N 0.000 description 1
- 229950006824 dieldrin Drugs 0.000 description 1
- NGPMUTDCEIKKFM-UHFFFAOYSA-N dieldrin Natural products CC1=C(Cl)C2(Cl)C3C4CC(C5OC45)C3C1(Cl)C2(Cl)Cl NGPMUTDCEIKKFM-UHFFFAOYSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 229940069096 dodecene Drugs 0.000 description 1
- 229920006351 engineering plastic Polymers 0.000 description 1
- GKIPXFAANLTWBM-UHFFFAOYSA-N epibromohydrin Chemical compound BrCC1CO1 GKIPXFAANLTWBM-UHFFFAOYSA-N 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 239000003456 ion exchange resin Substances 0.000 description 1
- 229920003303 ion-exchange polymer Polymers 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 235000013847 iso-butane Nutrition 0.000 description 1
- NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 description 1
- VUZPPFZMUPKLLV-UHFFFAOYSA-N methane;hydrate Chemical compound C.O VUZPPFZMUPKLLV-UHFFFAOYSA-N 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- BAVYZALUXZFZLV-UHFFFAOYSA-N mono-methylamine Natural products NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 1
- YKYONYBAUNKHLG-UHFFFAOYSA-N n-Propyl acetate Natural products CCCOC(C)=O YKYONYBAUNKHLG-UHFFFAOYSA-N 0.000 description 1
- LYGJENNIWJXYER-UHFFFAOYSA-N nitromethane Chemical compound C[N+]([O-])=O LYGJENNIWJXYER-UHFFFAOYSA-N 0.000 description 1
- CCCMONHAUSKTEQ-UHFFFAOYSA-N octadecene Natural products CCCCCCCCCCCCCCCCC=C CCCMONHAUSKTEQ-UHFFFAOYSA-N 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical compound [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 description 1
- 229920001515 polyalkylene glycol Polymers 0.000 description 1
- TVOIPJPTFTYKQM-UHFFFAOYSA-N propanedioic acid;zinc Chemical compound [Zn].OC(=O)CC(O)=O TVOIPJPTFTYKQM-UHFFFAOYSA-N 0.000 description 1
- FVSKHRXBFJPNKK-UHFFFAOYSA-N propionitrile Chemical compound CCC#N FVSKHRXBFJPNKK-UHFFFAOYSA-N 0.000 description 1
- 229940090181 propyl acetate Drugs 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000012429 reaction media Substances 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N sec-butylidene Natural products CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- ARCJQKUWGAZPFX-UHFFFAOYSA-N stilbene oxide Chemical compound O1C(C=2C=CC=CC=2)C1C1=CC=CC=C1 ARCJQKUWGAZPFX-UHFFFAOYSA-N 0.000 description 1
- 238000006557 surface reaction Methods 0.000 description 1
- UYISKGVFPMWFJV-UHFFFAOYSA-N terephthalic acid;zinc Chemical compound [Zn].OC(=O)C1=CC=C(C(O)=O)C=C1 UYISKGVFPMWFJV-UHFFFAOYSA-N 0.000 description 1
- 229940095068 tetradecene Drugs 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- LVBXEMGDVWVTGY-UHFFFAOYSA-N trans-2-octenal Natural products CCCCCC=CC=O LVBXEMGDVWVTGY-UHFFFAOYSA-N 0.000 description 1
- UBOXGVDOUJQMTN-UHFFFAOYSA-N trichloroethylene Natural products ClCC(Cl)Cl UBOXGVDOUJQMTN-UHFFFAOYSA-N 0.000 description 1
- 238000001291 vacuum drying Methods 0.000 description 1
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- HYRNDAFTGZPQBR-UHFFFAOYSA-L zinc 5-oxo-5-phenoxypentanoate Chemical compound [Zn++].[O-]C(=O)CCCC(=O)Oc1ccccc1.[O-]C(=O)CCCC(=O)Oc1ccccc1 HYRNDAFTGZPQBR-UHFFFAOYSA-L 0.000 description 1
- AGFGXVAAIXIOFZ-UHFFFAOYSA-L zinc;butanedioate Chemical compound [Zn+2].[O-]C(=O)CCC([O-])=O AGFGXVAAIXIOFZ-UHFFFAOYSA-L 0.000 description 1
- YNKYXJFHDLXPTI-UHFFFAOYSA-L zinc;hexanedioate Chemical compound [Zn+2].[O-]C(=O)CCCCC([O-])=O YNKYXJFHDLXPTI-UHFFFAOYSA-L 0.000 description 1
- 229910001928 zirconium oxide Inorganic materials 0.000 description 1
- 239000013096 zirconium-based metal-organic framework Substances 0.000 description 1
- PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-Caprolactone Chemical compound O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 0.000 description 1
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Abstract
Description
本出願は、2017年8月28日付韓国特許出願第10−2017−0108897号および2018年8月28日付韓国特許出願第10−2018−0101027号に基づいた優先権の利益を主張し、当該韓国特許出願の文献に開示されたすべての内容は本明細書の一部として含まれている。
前記ジルコニウム系助触媒は、ジルコニウムが含まれた金属有機構造体(Zr−metal organic framework,MOF)およびZr前駆体からなる群より選ばれたいずれか一つである有機亜鉛触媒の製造方法を提供する。
亜鉛ジカルボキシレート系化合物;および
前記亜鉛ジカルボキシレート系化合物の表面に担持または置換されたジルコニウム元素を含み、
前記ジルコニウム元素は、ジルコニウムが含まれた金属有機構造体(Zr−metal organic framework,MOF)およびZr前駆体からなる群より選ばれたいずれか一つのジルコニウム系助触媒から含まれる、有機亜鉛触媒を提供する。
発明の一実現例によれば、亜鉛前駆体を炭素数3〜20のジカルボン酸およびジルコニウム系助触媒と反応させる段階を含み、前記ジルコニウム系助触媒は、ジルコニウムが含まれた金属有機構造体(Zr−metal organic framework,MOF)およびZr前駆体からなる群より選ばれたいずれか一つである有機亜鉛触媒の製造方法が提供され得る。
一方、発明の一実施例によれば、亜鉛ジカルボキシレート系化合物;および
前記亜鉛ジカルボキシレート系化合物の表面に担持または置換されたジルコニウム元素を含み、
前記ジルコニウム元素は、ジルコニウムが含まれた金属有機構造体(Zr−metal organic framework,MOF)およびZr前駆体からなる群より選ばれたいずれか一つのジルコニウム系助触媒から含まれる、有機亜鉛触媒が提供され得る。
一方、発明のまた他の一実現例によれば、上述した有機亜鉛触媒の存在下にエポキシドおよび二酸化炭素を含む単量体を重合させる段階を含むポリアルキレンカーボネート樹脂の製造方法が提供される。
100ml容量の丸底フラスコで、50mlのトルエンに2.64g(20mmol)のグルタル酸および0.18gのUiO−66を加えて還流下に分散させた後、55℃の温度で30分加熱した。前記混合溶液に1.36gのZnO粒子を加えた後3時間撹拌した。
100ml容量の丸底フラスコで、50mlのトルエンに2.64g(20mmol)のグルタル酸および0.36gのUiO−66を加えて還流下に分散させた後、55℃の温度で30分加熱した。前記混合溶液に1.36gのZnO粒子を加えた後3時間撹拌した。
100ml容量の丸底フラスコで、50mlのトルエンに2.64g(20mmol)のグルタル酸および0.72gのUiO−66を加えて還流下に分散させた後、55℃の温度で30分加熱した。前記混合溶液に1.36gのZnO粒子を加えた後3時間撹拌した。
100ml容量の丸底フラスコで、50mlのトルエンに2.64g(20mmol)のグルタル酸および0.04gのUiO−66を加えて還流下に分散させた後、55℃の温度で30分加熱した。前記混合溶液に1.36gのZnO粒子を加えた後3時間撹拌した。
100ml容量の丸底フラスコで、50mlのトルエンに2.64g(20mmol)のグルタル酸および0.004gのUiO−66を加えて還流下に分散させた後、55℃の温度で30分加熱した。前記混合溶液に1.36gのZnO粒子を加えた後3時間撹拌した。
100ml容量の丸底フラスコで、50mlのトルエンに2.64g(20mmol)のグルタル酸および0.36gのZrSO4を加えて還流下に分散させた後、55℃の温度で30分加熱した。前記混合溶液に1.36gのZnO粒子を加えた後3時間撹拌した。
100ml容量の丸底フラスコで、50mlのトルエンに2.64g(20mmol)のグルタル酸を加えて還流下に分散させた後、55℃の温度で30分加熱した。前記混合溶液に1.36gのZnO粒子を加えた後3時間撹拌した。
100ml容量の丸底フラスコで、50mlのトルエンに2.64g(20mmol)のグルタル酸および0.1gのMgCl2を加えて還流下に分散させた後、55℃の温度で30分加熱した。前記混合溶液に1.36gのZnO粒子を加えた後3時間撹拌した。
UiO−66の代わりにコバルト酸化物を用いることを除いては、実施例1と同様の方法により亜鉛グルタラート担持触媒を製造した。
実施例1〜6および比較例1〜3の触媒を用いて次の方法でポリエチレンカーボネートを製造した。
有機亜鉛触媒の製造時、ZnGAに対する助触媒(UiO−66)の含有量別に添加されるZrの重量%に応じた表面元素の成分比を測定した。その結果は表2に示した(atomic重量%)。また、各試料のZr 3d narrow scan spectrum結果を図1に示した。
Claims (14)
- 亜鉛前駆体を炭素数3〜20のジカルボン酸およびジルコニウム系助触媒と反応させる段階を含み、
前記ジルコニウム系助触媒は、ジルコニウムが含まれた金属有機構造体(Zr−metal organic framework,MOF)およびZr前駆体からなる群より選ばれたいずれか一つである、有機亜鉛触媒の製造方法。 - 前記ジルコニウムが含まれた金属有機構造体は、UiO−66(Zirconium 1,4−dicarboxybenzene MOF)、UiO−66−NH2、UiO−66−NH3+、UiO−67、UiO−68およびNu−1000からなる群より選ばれた1種以上である、請求項1に記載の有機亜鉛触媒の製造方法。
- 前記Zr前駆体は、ZrSO4、ジルコニウムアセテート、ジルコニウムヨージド、ジルコニウムフルオライド、ジルコニウムクロリド、ジルコニウムアセチルアセトネート、ジルコニウムブトキシド、ジルコニウムプロポキシドおよびZrO2からなる群より選ばれた1種以上である、請求項1に記載の有機亜鉛触媒の製造方法。
- 前記ジルコニウム系助触媒は、亜鉛前駆体1モルに対して0.1mモル〜0.5モル比で用いる、請求項1に記載の有機亜鉛触媒の製造方法。
- ポリアルキレンカーボネート樹脂の合成に用いられる、請求項1に記載の有機亜鉛触媒の製造方法。
- 前記亜鉛前駆体は、酸化亜鉛(ZnO)、硫酸亜鉛(ZnSO4)、塩素酸亜鉛(Zn(ClO3)2)、硝酸亜鉛(Zn(NO3)2)、酢酸亜鉛(Zn(OAc)2)、および水酸化亜鉛(Zn(OH)2)からなる群より選ばれた1種以上の化合物を含み;
前記炭素数3〜20のジカルボン酸は、マロン酸、グルタル酸、コハク酸、アジピン酸、テレフタル酸、イソフタル酸、ホモフタル酸、およびフェニルグルタル酸からなる群より選ばれた1種以上の化合物を含む、請求項1に記載の有機亜鉛触媒の製造方法。 - 前記反応は、トルエン、ヘキサン、ジメチルホルムアミド、エタノール、および水からなる群より選ばれた1種以上の溶媒の存在下で行われる、請求項1に記載の有機亜鉛触媒の製造方法。
- 亜鉛ジカルボキシレート系化合物;および
前記亜鉛ジカルボキシレート系化合物の表面に担持または置換されたジルコニウム元素を含み、
前記ジルコニウム元素は、ジルコニウムが含まれた金属有機構造体(Zr−metal organic framework,MOF)およびZr前駆体からなる群より選ばれたいずれか一つのジルコニウム系助触媒から含まれる、有機亜鉛触媒。 - 前記ジルコニウムが含まれた金属有機構造体は、UiO−66(Zirconium 1,4−dicarboxybenzene MOF)、UiO−66−NH2、UiO−66−NH3+、UiO−67、UiO−68およびNu−1000からなる群より選ばれた1種以上である、請求項8に記載の有機亜鉛触媒。
- 前記Zr前駆体は、ZrSO4、ジルコニウムアセテート、ジルコニウムヨージド、ジルコニウムフルオライド、ジルコニウムクロリド、ジルコニウムアセチルアセトネート、ジルコニウムブトキシド、ジルコニウムプロポキシドおよびZrO2からなる群より選ばれた1種以上である、請求項8に記載の有機亜鉛触媒。
- ポリアルキレンカーボネート樹脂の合成に用いられる、請求項8に記載の有機亜鉛触媒。
- 前記亜鉛ジカルボキシレート系化合物の表面でのジルコニウム元素の含有量は、有機亜鉛触媒を構成する全体元素比の総重量を基準に0.01〜5重量%である、請求項8に記載の有機亜鉛触媒。
- 前記亜鉛ジカルボキシレート系化合物は、亜鉛前駆体と炭素数3〜20のジカルボン酸の反応生成物であり;
前記亜鉛前駆体は、酸化亜鉛(ZnO)、硫酸亜鉛(ZnSO4)、塩素酸亜鉛(Zn(ClO3)2)、硝酸亜鉛(Zn(NO3)2)、酢酸亜鉛(Zn(OAc)2)、および水酸化亜鉛(Zn(OH)2)からなる群より選ばれた1種以上の化合物を含み;
前記炭素数3〜20のジカルボン酸は、マロン酸、グルタル酸、コハク酸、アジピン酸、テレフタル酸、イソフタル酸、ホモフタル酸、およびフェニルグルタル酸からなる群より選ばれた1種以上の化合物を含む、請求項8に記載の有機亜鉛触媒。 - 請求項8に記載の有機亜鉛触媒の存在下にエポキシドおよび二酸化炭素を含む単量体を重合させる段階を含む、ポリアルキレンカーボネート樹脂の製造方法。
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