微波与传统水热法合成丙酸锌
DOI:
CSTR:
作者:
作者单位:

作者简介:

通讯作者:

中图分类号:

TS202.3

基金项目:

“绿色催化与反应工程”湖南省高等学校重点实验室开放课题(2009LC002)


Synthesis of Zinc Propionate by Microwave and Conventional Hydrothermal Method
Author:
Affiliation:

Fund Project:

  • 摘要
  • |
  • 图/表
  • |
  • 访问统计
  • |
  • 参考文献
  • |
  • 相似文献
  • |
  • 引证文献
  • |
  • 资源附件
  • |
  • 文章评论
    摘要:

    采用微波水热法和传统水热法以氧化锌和丙酸为原料、去离子水为溶剂成功合成了丙酸锌 (C6H10O4Zn)。对比考察了两种合成方法中单因素(反应温度、反应时间、丙酸/氧化锌摩尔比、去离子水量)对丙酸锌产率的影响;利用EDTA络合滴定、元素分析仪(EA)、红外光谱仪(FT-IR)和热重分析仪(TG)分析了丙酸锌的组成与结构。结果表明,在最优化反应条件下,微波水热法和传统水热法合成丙酸锌的产率分别为94.06%和87.34 %;与传统水热法相比,微波水热法对丙酸锌制备过程具有强化作用。采用两种不同方法所合成的样品都具有典型的丙酸锌结构,组成略有差异,微波条件下的丙酸锌含更多结晶水,热稳定性更好。

    Abstract:

    With the water as the solvent, zinc propionate (C6H10O4Zn) was successfully synthesized from propionic acid and zinc oxide as the raw material by microwave and conventional hydrothermal methods. The effects of reaction temperature, time, molar ratio of propionic acid/zinc oxide and dosage of deionized water in the two synthesis process on the yield of C6H10O4Zn were studied through parallel experiments. The product was characterized by means of EDTA complexometric method, EA, FT-IR and TG. The results showed that the yields of C6H10O4Zn by microwave and conventional hydrothermal methods were 94.06% and 87.34%, respectively, under the optimal synthetic conditions. Compared with conventional hydrothermal method, microwave hydrothermal method had a great strengthening effect on synthesis of C6H10O4Zn. The synthesized product possessed the typical structure of C6H10O4Zn, and the composition of C6H10O4Zn was nearly the same for the two synthesis methods. However, C6H10O4Zn obtained by microwave hydrothermal method had more crystallization water and better thermal stability than that from conventional hydrothermal method.

    参考文献
    相似文献
    引证文献
引用本文

张娟娟,谢放华,陈晓宁,李焙,郭鑫鹏,刘嘉惠.微波与传统水热法合成丙酸锌[J].精细化工,2015,32(2):0

复制
分享
文章指标
  • 点击次数:
  • 下载次数:
  • HTML阅读次数:
  • 引用次数:
历史
  • 收稿日期:2014-07-30
  • 最后修改日期:2014-09-24
  • 录用日期:2014-09-26
  • 在线发布日期: 2015-01-07
  • 出版日期:
文章二维码