第 44 卷第 6 期Vol. 44 No. 6
2014 年 12 月Dec 2014

所属栏目:功能材料

硫酸亚铁-过氧化氢体系绿色合成聚苯胺的研究
潘 珍1,邱 野1,孟 勇1,2*,李 明1,尹笃林2 (1. 湖南师范大学 资源循环综合技术研究中心, 湖南 长沙 410081; 2. 石化新材料与资源精细利用国家地方联合工程实验室, 湖南 长沙 410081)
摘 要:以硫酸亚铁-过氧化氢为绿色催化氧化体系合成了聚苯胺。探讨了硫酸亚铁浓度、过氧化氢的用量、反应体系酸度、反应温度、苯胺浓度等工艺条件对聚苯胺收率的影响,分析了该体系中苯胺可能的聚合机理,推测并初步验证了反应液重复使用的可行性。在亚铁浓度为3.36×10-4 mol/L,n(过氧化氢)∶n(苯胺)=1.4∶1.0,反应温度为70℃,H+(硫酸)浓度1.5 mol/L,单体浓度0.9 mol/L条件下,聚苯胺收率为77.2%。
关键词:绿色合成;过氧化氢;硫酸亚铁;聚苯胺;苯胺
中图分类号:TQ21  文献标识码:A  文章编号:1009-9212(2014)06-0067-05
Study on Green Synthesis of Polyaniline by Ferrous Sulfate and Hydrogen Peroxide System
PAN Zhen1, QIU Ye1, MENG Yong1,2*, LI Ming1, YIN Du-lin2 (1. Research Center of Resource Recycling Integrated Technology, Hunan Normal University, Changsha 410081, China; 2. Key Laboratory of Resource Fine-Processing and Advanced Materials, Universities of Hunan Province, College of Chemistry and Chemical Engineering, Hunan Normal University, Changsha 410081, China)
Abstract:In this paper, polyaniline was synthesized in a green way under catalysis of ferrous sulfate and hydrogen peroxide. The effects of the amount of hydrogen peroxide, the concentration of ferrous sulfate, the acidity, the reaction temperature and the concentration of aniline(Ani)were studied. A possible mechanism of the aniline polymerization was proposed. The feasibility of reusing the reaction liquid was conjectured from the polymerization mechanism, and it was verified by experiments. The obtained polyaniline was characterized by IR spectra, and the characteristic absorption peaks of polyaniline could be found. The polyaniline was prepared in 77.2% yield under the following conditions: concentration of Fe2+ 3.36×10-4 mol/L, n(H2O2):n(Ani)=1.4:1.0, reaction temperature 70℃, concentration of H+(sulfuric acid) 1.5 mol/L, concentration of aniline monomer 0.9 mol/L.
Key words:green synthesis; hydrogen peroxide; ferrous sulfate; polyaniline; aniline
作者简介: 潘 珍(1989-),女,湖南长沙人,硕士研究生,研究方向:高分子还原材料的制备及应用(E-mail:panz1989@163.com)。
联 系 人:孟 勇,副教授,研究方向:废水、净水处理剂及其工艺研究(E-mail:mengyong76@163.com)。
收稿日期: 2014-10-1