Preparation of crown ether complexing highly active double metal cyanide catalysts and copolymerization of CO2 and propylene oxide
被引:14
|
作者:
Zhang, Min
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机构:
Foshan Univ, Coll Food & Hort Sci, Foshan 528231, Guangdong, Peoples R ChinaFoshan Univ, Coll Food & Hort Sci, Foshan 528231, Guangdong, Peoples R China
Zhang, Min
[1
]
Yang, Yong
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机构:
Chinese Acad Sci, Guangzhou Inst Chem, Guangzhou 510650, Guangdong, Peoples R China
Univ Chinese Acad Sci, Beijing 100049, Peoples R ChinaFoshan Univ, Coll Food & Hort Sci, Foshan 528231, Guangdong, Peoples R China
Yang, Yong
[2
,3
]
Chen, Liban
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机构:
Chinese Acad Sci, Guangzhou Inst Chem, Guangzhou 510650, Guangdong, Peoples R ChinaFoshan Univ, Coll Food & Hort Sci, Foshan 528231, Guangdong, Peoples R China
Chen, Liban
[2
]
机构:
[1] Foshan Univ, Coll Food & Hort Sci, Foshan 528231, Guangdong, Peoples R China
[2] Chinese Acad Sci, Guangzhou Inst Chem, Guangzhou 510650, Guangdong, Peoples R China
[3] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
Double metal cyanide (DMC) catalysts are generally prepared by coprecipitation of potassium hexacyanocobaltate(III) with zinc chloride followed by complexation with tert-butanol, and these materials have been used for several decades in the copolymerization of CO2 and epoxides. However, the catalytic efficiency of DMC catalysts can be adversely affected by the presence of excess K+, and the preparation of these catalysts can therefore become complicated and time-consuming because of the multiple washing and centrifugation stages required for the removal of the excess K+. In this study, 18-crown-6 ether was used as an effective co-complexing agent for the removal of K+. A series of DMCs containing 18-crown-6 were prepared with different quantities of the crown ether and different washing times. The resulting crown ether-complexing catalysts (CDMCs) and DMC catalysts without crown ether were characterized by Fourier transform infrared spectroscopy, scanning electron microscopy, thermogravimetric analysis-IR and X-ray diffraction. These characterization results showed that the inclusion of 18-crown-6 allowed for the formation of uniform and highly dispersed CDMC catalysts. In contrast, the DMC catalysts prepared in the absence of 18-crown-6 became uneven and delaminated during the purification by centrifugation, with high- and low-density portions of the material forming on the bottom and top of the catalyst cakes, respectively. The inclusion of 18-crown-6 not only trapped K+ but also participated in the complexion process. The complexion of tert-BuOH and 18-crown-6 led to a less crystalline form of the CDMC catalyst. Elemental analysis revealed that CDMC1 contained 1.2% K+. The copolymer was obtained by the copolymerization of CO2 with propylene oxide using CDMC3 catalyst, which was superior to the copolymer prepared using DMC1. CDMC3 was as active as DMC2 prepared without the crown ether but with seven washing steps. A hypothetical two-stage catalytic mechanism was proposed. (C) 2015, Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by Elsevier B.V. All rights reserved.
机构:
Pusan Natl Univ, Dept Polymer Sci & Engn, BK21 PLUS Ctr Adv Chem Technol, Busan 609735, South KoreaPusan Natl Univ, Dept Polymer Sci & Engn, BK21 PLUS Ctr Adv Chem Technol, Busan 609735, South Korea
Tran, Chinh Hoang
Kim, Sun A.
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Pusan Natl Univ, Dept Polymer Sci & Engn, BK21 PLUS Ctr Adv Chem Technol, Busan 609735, South KoreaPusan Natl Univ, Dept Polymer Sci & Engn, BK21 PLUS Ctr Adv Chem Technol, Busan 609735, South Korea
Kim, Sun A.
Moon, Yeji
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Pusan Natl Univ, Dept Polymer Sci & Engn, BK21 PLUS Ctr Adv Chem Technol, Busan 609735, South KoreaPusan Natl Univ, Dept Polymer Sci & Engn, BK21 PLUS Ctr Adv Chem Technol, Busan 609735, South Korea
Moon, Yeji
Lee, Yechan
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Pusan Natl Univ, Dept Polymer Sci & Engn, BK21 PLUS Ctr Adv Chem Technol, Busan 609735, South KoreaPusan Natl Univ, Dept Polymer Sci & Engn, BK21 PLUS Ctr Adv Chem Technol, Busan 609735, South Korea
Lee, Yechan
Ryu, Hyun Mo
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Pusan Natl Univ, Dept Polymer Sci & Engn, BK21 PLUS Ctr Adv Chem Technol, Busan 609735, South KoreaPusan Natl Univ, Dept Polymer Sci & Engn, BK21 PLUS Ctr Adv Chem Technol, Busan 609735, South Korea
Ryu, Hyun Mo
Baik, Joon Hyun
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机构:
Res Inst Ind Sci & Technol, Climate & Energy Res Grp, 67 Cheongam Ro, Pohang 37673, South KoreaPusan Natl Univ, Dept Polymer Sci & Engn, BK21 PLUS Ctr Adv Chem Technol, Busan 609735, South Korea
Baik, Joon Hyun
Hong, Sung Chul
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机构:
Sejong Univ, Dept Nanotechnol & Adv Mat Engn, 209 Neungdong Ro, Seoul 143747, South KoreaPusan Natl Univ, Dept Polymer Sci & Engn, BK21 PLUS Ctr Adv Chem Technol, Busan 609735, South Korea
Hong, Sung Chul
Kim, Il
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Pusan Natl Univ, Dept Polymer Sci & Engn, BK21 PLUS Ctr Adv Chem Technol, Busan 609735, South KoreaPusan Natl Univ, Dept Polymer Sci & Engn, BK21 PLUS Ctr Adv Chem Technol, Busan 609735, South Korea
机构:
Hainan Normal Univ, Coll Chem & Chem Engn, Haikou 571158, Hainan, Peoples R ChinaHainan Normal Univ, Coll Chem & Chem Engn, Haikou 571158, Hainan, Peoples R China
Lin Qiang
Guo Zhifang
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机构:
Hainan Normal Univ, Coll Chem & Chem Engn, Haikou 571158, Hainan, Peoples R ChinaHainan Normal Univ, Coll Chem & Chem Engn, Haikou 571158, Hainan, Peoples R China
Guo Zhifang
Pan Lisha
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h-index: 0
机构:
Hainan Univ, Hainan Prov Fine Chem Engn Res Ctr, Inst Mat & Chem Engn, Haikou 570228, Hainan, Peoples R ChinaHainan Normal Univ, Coll Chem & Chem Engn, Haikou 571158, Hainan, Peoples R China
Pan Lisha
Xiang Xue
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机构:
Hainan Normal Univ, Coll Chem & Chem Engn, Haikou 571158, Hainan, Peoples R ChinaHainan Normal Univ, Coll Chem & Chem Engn, Haikou 571158, Hainan, Peoples R China
机构:
Shanghai Res Inst Petrochem Technol, SINOPEC, Shanghai 201208, Peoples R ChinaShanghai Res Inst Petrochem Technol, SINOPEC, Shanghai 201208, Peoples R China
Lu, YG
Tu, JJ
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Shanghai Res Inst Petrochem Technol, SINOPEC, Shanghai 201208, Peoples R ChinaShanghai Res Inst Petrochem Technol, SINOPEC, Shanghai 201208, Peoples R China
Tu, JJ
Jin, H
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机构:
Shanghai Res Inst Petrochem Technol, SINOPEC, Shanghai 201208, Peoples R ChinaShanghai Res Inst Petrochem Technol, SINOPEC, Shanghai 201208, Peoples R China
Jin, H
Cai, LP
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Shanghai Res Inst Petrochem Technol, SINOPEC, Shanghai 201208, Peoples R ChinaShanghai Res Inst Petrochem Technol, SINOPEC, Shanghai 201208, Peoples R China
Cai, LP
Wang, RW
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Shanghai Res Inst Petrochem Technol, SINOPEC, Shanghai 201208, Peoples R ChinaShanghai Res Inst Petrochem Technol, SINOPEC, Shanghai 201208, Peoples R China
Wang, RW
[J].
ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY,
2002,
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: U377
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