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Synthesis of cementite-dispersed carbons by pressure pyrolysis of organoiron copolymers
Authors:Toshinobu Yogo  Hisanori Yokoyama  Shigeharu Naka  Shin-Ichi Hirano
Affiliation:(1) Synthetic Crystal Research Laboratory, Nagoya University, Furo-cho, Chikusa-ku, 464 Nagoya, Japan;(2) Department of Applied Chemistry, Faculty of Engineering, Nagoya University, Furo-cho, Chikusa-ku, 464 Nagoya, Japan
Abstract:Cementite-dispersed carbons were synthesized by pressure pyrolysis of divinylbenzene-vinylferrocene and styrene-vinylferrocene copolymer at temperatures below 600° C and the pressure of 125 MPa. The pyrolysis process of both copolymers was analysed by infrared spectra and magnetization of the pyrolysed substances. The absorption band of iron-carbon bond of divinylbenzene-vinylferrocene copolymer decreased on increasing its pyrolysis temperature from 300 to 450° C and finally disappeared at 500° C. The carbonization of divinylbenzene-vinylferrocene proceeded more rapidly than styrene-vinylferrocene at temperatures between 450 and 500° C. Styrene-vinylferrocene was heat-treated at 250° C for 2 h under 100 MPa affording a paramagnetic product, whereas the paramagnetic character of divinylbenzene-vinylferrocene was revealed after heat-treatment at 380° C. The saturation magnetization of cementite-dispersed carbon synthesized from both kinds of copolymers was comparable when the pressure pyrolysis was carried out at temperatures between 520 to 600° C at 125 MPa. The saturation magnetization of cementite-dispersed carbon formed at 550° C under 125 MPa was correlated linearly with the iron content in carbon. Threedimensional cross-linked divinylbenzene-vinylferrocene copolymer gave the highly dispersed cementite particles less than 50 nm with the coercive force of 950 Oe. On the other hand, the larger particle size of cementite up to 120 nm and the lower coercive force about 400 Oe were obtained in carbon matrix prepared by the pressure pyrolysis of styrene-vinylferrocene copolymer.
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