Qiong Hou

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Name: 侯琼; Qiong Hou
Organization: South China Normal University , China
Department:
Title: Associate Professor(PhD)

TOPICS

Co-reporter:Qi Li;Yiquan Chen;Xinpu Song;Yingpeng Xie;Guang Shi
Journal of Applied Polymer Science 2015 Volume 132( Issue 12) pp:
Publication Date(Web):
DOI:10.1002/app.41677

ABSTRACT

By adjusting the molar ratios of antistatic monomer of octyl phenol ethylene oxide acrylate (denoted as AS), rigid monomer of methyl methacrylate (denoted as MMA), and flame-retardant monomer of 2-(phosphoryloxymethyl oxyethylene) acrylate (denoted as FR), a series of flame-retardant antistatic copolymers poly (octyl phenol ethylene oxide acrylate-co-methyl methacrylate-co-phosphoryloxymethyl oxyethylene acrylate) (donated as AMF) were synthesized through radical polymerization. Among the obtained copolymers, two copolymers, AMF162 (the feed molar ratio of AS, MMA, and FR as 1 : 6 : 2) and AMF1104 (the feed molar ratio of AS, MMA, and FR as 1 : 10 : 4) with different concentrations were added into polypropylene (PP) to prepare PP-AMF162 and PP-AMF1104 series of composites. The thermal stability, limiting oxygen index, the antistatic property, and mechanical properties of PP composites were tested and analyzed. PP-AMF162 series composites have excellent antistatic effect. When the AMF162 content was equal to or <15 wt %, the impact strength of PP-AMF162 composites was higher than that of pure PP. The results indicated that copolymer AMF162 was a suitable flame-retardant and antistatic additive for PP. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015, 132, 41677.

Co-reporter:Tao Jia;Kang Xiong;Qi Li
Journal of Materials Science: Materials in Electronics 2014 Volume 25( Issue 4) pp:1639-1646
Publication Date(Web):2014 April
DOI:10.1007/s10854-014-1777-6
Two novel benzo[1,2-b:3,4-b′]thiophene-based copolymers (namely, PBDT-TPABTBn and PBDT-BTCz) with a pendent acceptor were synthesized through Pd-catalyzed Stille coupling reactions for use in organic photovoltaic devices. To study the photovoltaic properties of the resulting copolymers, polymer solar cells were fabricated with the copolymers as electron donors and [6,6]-phenyl-C71-butyric acid methyl ester as an electron acceptor. The obtained devices based on PBDT-TPABTBn and PBDT-BTCz exhibited power conversion efficiencies of 1.62 % (Voc = 0.94 V, Jsc = 4.74 mA cm−2, FF = 0.39) and 0.95 % (Voc = 0.64 V, Jsc = 4.16 mA cm−2, FF = 0.36), respectively. Results indicated that the two copolymers were the promising donor candidates for polymer solar cell applications.
Benzenamine, 4-[3-dodecyl-5-(tributylstannyl)-2-thienyl]-N,N-diphenyl-
Benzenamine, 4-[(1E)-2-(7-bromo-2,1,3-benzothiadiazol-4-yl)ethenyl]-N-[4-[(1E)-2-(7-bromo-2,1,3-benzothiadiazol-4-yl)ethenyl]phenyl]-N-phenyl-
Benzaldehyde, 4-[[4-[(1E)-2-(7-bromo-2,1,3-benzothiadiazol-4-yl)ethenyl]phenyl]phenylamino]-
Propanedinitrile, 2-[[4-[[4-[(1E)-2-(7-bromo-2,1,3-benzothiadiazol-4-yl)ethenyl]phenyl]phenylamino]phenyl]methylene]-
Propanedinitrile, 2-[[4-[[4-[(1E)-2-[7-[5-[4-(diphenylamino)phenyl]-4-dodecyl-2-thienyl]-2,1,3-benzothiadiazol-4-yl]ethenyl]phenyl]phenylamino]phenyl]methylene]-
Benzeneacetonitrile, α-[[4-[[4-[(1E)-2-[7-[5-[4-(diphenylamino)phenyl]-4-dodecyl-2-thienyl]-2,1,3-benzothiadiazol-4-yl]ethenyl]phenyl]phenylamino]phenyl]methylene]-4-nitro-, (αE)-
Benzeneacetonitrile, α,α'-[[4,8-bis[(2-ethylhexyl)oxy]benzo[1,2-b:4,5-b']dithiophene-2,6-diyl]bis[2,1,3-benzothiadiazole-7,4-diyl-(1E)-2,1-ethenediyl-4,1-phenylene(phenylimino)-4,1-phenylenemethylidyne]]bis[4-nitro-, (αE,α'E)-
Benzenamine, 4,4'-thiazolo[5,4-d]thiazole-2,5-diylbis[N,N-bis(4-bromophenyl)-
Benzenamine, 4,4'-thiazolo[5,4-d]thiazole-2,5-diylbis[N,N-bis[4-(4-hexyl-2-thienyl)phenyl]-
Benzenamine, 4,4'-thiazolo[5,4-d]thiazole-2,5-diylbis[N,N-bis[4-[5-[4-(diphenylamino)phenyl]-4-dodecyl-2-thienyl]phenyl]-