叔丁基过氧化氢对聚丙烯腈环化反应的影响

徐赛男, 徐樑华, 童元建*

化工新型材料 ›› 2022, Vol. 50 ›› Issue (3) : 192 -195.

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化工新型材料 ›› 2022, Vol. 50 ›› Issue (3) : 192-195. DOI: 10.19817/j.cnki.issn1006-3536.2022.03.039
科学研究

叔丁基过氧化氢对聚丙烯腈环化反应的影响

    徐赛男, 徐樑华, 童元建*
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Influence of tert-butyl hydroperoxide on cyclization of PAN

  • Xu Sainan, Xu Lianghua, Tong Yuanjian
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摘要

为加快聚丙烯腈(PAN)的预氧化速度,提高碳化收率,使用分解温度较高的叔丁基过氧化氢(TBHP)对PAN进行改性处理,得到TBHP/PAN改性膜,通过差示扫描量热仪、热重分析仪研究了TBHP对PAN环化反应的影响。结果表明,TBHP/PAN改性膜的环化反应起始温度为175℃左右,较未改性PAN膜降低了约90℃,最大放热峰值温度从277℃(未改性PAN膜)降低到260℃,放热峰宽化明显。环化反应动力学研究表明,TBHP/PAN改性膜的环化反应活化能为167.43kJ/mol,指前因子为1.34×1013。预氧化处理后氮气气氛下TBHP/PAN改性膜700℃的热失重率为33.13%,较未改性PAN膜降低了6.12%。

Abstract

To accelerate the stabilization process of polyacrylonitrile (PAN) and increase carbonization yield,tert-butyl hydroperoxide (TBHP) was used to modify PAN.The effects of TBHP on cyclization of PAN was studied using DSC and TG.The results showed that the initiate temperature of the cyclization for PAN was about 175℃,90℃ lower than that of unmodified PAN.The exothermic peak temperature decreased from 277℃ for unmodified PAN to 260℃ for TBHP/PAN with broader peak width.Kinetic analysis results indicated that the activation energy of cyclic reaction for TBHP/PAN was 167.43kJ/mol,and the pre-exponential factor was 1.34×1013.The weight loss in N2 of the stabilized TBHP/PAN was 33.13%,6.12% less than that of unmodified PAN.

关键词

叔丁基过氧化氢 / 聚丙烯腈 / 环化反应 / 改性

Key words

tert-butyl hydroperoxide / polyacrylonitrile / cyclization / modification

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叔丁基过氧化氢对聚丙烯腈环化反应的影响[J]. 化工新型材料, 2022, 50(3): 192-195 DOI:10.19817/j.cnki.issn1006-3536.2022.03.039

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参考文献

[1] Ouyang Q,Wang X H,Wang X L,et al.Simultaneous DSC/TG analysis on the thermal behavior of PAN polymers prepared by aqueous free-radical polymerization[J].Polymer Degradation and Stability,2016,130:320-327.
[2] Mittal J,Mathur R B,Bahl O P.Post spinning treatment of PAN fibers using succinic acid to produce high performance carbon fibers[J].Carbon,1998,36(7/8):893-897.
[3] Tong Y J,Zhang B W,Li C Q,et al.Copolymerization of acrylonitrile/1-vinyl-3-ethylimidazolium bromide,and rheological,thermal properties of the copolymer[J].Transactions of Tianjin University,2019,25:85-90.
[4] Jeremy D M,Jeffrey S W.Thermo-oxidative stabilization of polyacrylonitrile and its copolymers:effect of molecular weight,dispersity,and polymerization pathway[J].Polymer Degradation and Stability,2016,125:76-86.
[5] Tan L,Wan A.Structural changes of polyacrylonitrile precursor fiber induced by γ-ray irradiation[J].Materials Letters,2011,65(19):3109-3111.
[6] Liu L Q,Chen H F,Pan D.Modification of polyacrylonitrile precursor fiber with hydrogen peroxide[J].Fibers and Polymers,2012,13(5):585-592.
[7] Mathur R B,Bahl O P.Post spinning treatment of PAN fibers using succinic acid to produce high performance carbon fibers[J].Carbon,1998,36(7/8):893-897.
[8] 刘杰,杜大艳,梁杰英,等.化学改性对聚丙烯腈纤维及预氧纤维结构性能的影响[J].高科技纤维与应用,2009,34(5):21-25;54-55.
[9] 王强,朱波,高学平,等.混酸处理对预氧化聚丙烯腈纤维结构和性能的影响[J].高分子材料科学与工程,2006,22(4):162-164;168.
[10] 孙同庆,吕春祥,李永红,等.硼酸改性对聚丙烯腈纤维预氧化的影响[J].合成纤维,2016,45(6):38-41.
[11] Rahaman M S,Ismail A F,Mustafa A.A review of heat treatment on polyacrylonitrile fiber[J].Polymer Degradation and Stability,2007,92(8):1421-1432.
[12] 郭鹏宗,白玉俊.KMnO4改性对聚丙烯腈原丝结构和性能的影响[J].功能材料,2007(11):1800-1801;1805.
[13] 赵雅娴,武帅,康宸,等.H2O2改性对聚丙烯腈原丝化学结构的影响[J].复合材料学报,2019,36(1):85-95.
[14] Xiao S J,Cao W Y,Wang B.Mechanism and kinetics of oxidation during the thermal stabilization of polyacrylonitrile fibers[J].Journal of Applied Polymer Science,2013,127(4):3198-3203.
[15] Shahram A,Ahmad Z.Quantitative analysis of the effects of comonomers and heating conditions on the stabilization reactions of polyacrylonitrile fibers as carbon fiber precursors[J].Polymer Degradation and Stability,2017,139:107-116.
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