基于官能团非等活性假设的尼龙66盐溶液聚合动力学模型

王颖; 林程; 崔晶; 奚桢浩; 赵玲

doi:10.11949/0438-1157.20200208

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基于官能团非等活性假设的尼龙66盐溶液聚合动力学模型

催化、动力学与反应器 | 更新时间：2026-07-24

- 基于官能团非等活性假设的尼龙66盐溶液聚合动力学模型
- New kinetic model for polymerization process of nylon 66 salt solution based on functional group non-isoactivity
- 化工学报 2020年71卷第11期页码：5208-5215
- 作者机构：
  
  1.华东理工大学化工学院，化学工程联合国家重点实验室，上海 200237
  2.中国石化上海石油化工研究院，上海 201208
  3.新疆大学化学与化工学院，石油天然气精细化工教育部重点实验室，新疆乌鲁木齐 830046
- 作者简介：
  
  王颖（1995—），女，硕士研究生，wangying_hola@163.com
  奚桢浩（1981—），男，博士，副教授，zhhxi@ecust.edu.cn
- 基金信息：
  
  十三五国家重点研发计划项目(2016YFB0303001);国家自然科学基金项目(21878256);中央高校基本科研业务费专项资金(22221817014)
- DOI：10.11949/0438-1157.20200208
  中图分类号： TQ 316.4
- 收稿：2020-02-28，
  
  修回：2020-05-23，
  
  网络首发：2020-11-03，
  
  纸质出版：2020-11-05
- 稿件说明：
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王颖, 林程, 崔晶, 奚桢浩, 赵玲. 基于官能团非等活性假设的尼龙66盐溶液聚合动力学模型[J]. 化工学报, 2020, 71(11): 5208-5215

WANG Ying, LIN Cheng, CUI Jing, XI Zhenhao, ZHAO Ling. New kinetic model for polymerization process of nylon 66 salt solution based on functional group non-isoactivity[J]. CIESC Journal, 2020, 71(11): 5208-5215
王颖, 林程, 崔晶, 奚桢浩, 赵玲. 基于官能团非等活性假设的尼龙66盐溶液聚合动力学模型[J]. 化工学报, 2020, 71(11): 5208-5215 DOI： 10.11949/0438-1157.20200208.

WANG Ying, LIN Cheng, CUI Jing, XI Zhenhao, ZHAO Ling. New kinetic model for polymerization process of nylon 66 salt solution based on functional group non-isoactivity[J]. CIESC Journal, 2020, 71(11): 5208-5215 DOI： 10.11949/0438-1157.20200208.

摘要

尼龙66盐溶液聚合过程属于动力学控制过程。基于官能团非等活性假设，在Mallon酸催化3阶反应动力学模型基础上，引入尼龙盐脱水反应，建立了新的尼龙66盐溶液聚合反应动力学模型，拟合得到了关键反应动力学模型参数，其中盐脱水反应速率常数为8.17×10

-3

kg∙mol

-1

∙h

-1

、活化能为19859 cal∙mol

-1

。与Mallon模型相比，新模型拟合效果更优，可在更宽的温度和水含量范围内准确预测聚合过程的变化。模拟仿真发现，盐脱水反应对聚合过程有重要影响，低温和高水含量下尼龙盐浓度高，聚合效率低；适当提高反应温度或降低初始水含量可以加快尼龙盐脱水反应，从而提高聚合反应效率。新的尼龙盐聚合动力学建模方法不仅适用于尼龙66，也可应用于尼龙1212等盐溶液聚合体系。

Abstract

The polymerization process of nylon 66 salt solution is a dynamically controlled process. Based on the assumption of unequal activity of functional carboxyl and amido groups

a new nylon 66 salt solution polymerization kinetic model was established by introducing the nylon salt dehydration reaction to the acid-catalyzed third-order reaction kinetic model and fitted to obtain the corresponding key kinetic parameters. The fitted salt dehydration reaction rate constant was 8.17×10

-3

kg∙mol

-1

∙h

-1

while the activation energy was 19859 cal∙mol

-1

respectively. Compared with Mallon model

the new developed model has a better fitting effect and can accurately predict the change of the polymerization process in a wider range of temperature and water content. Simulation results showed that salt dehydration reaction has an important effect on the polymerization process and the polymerization efficiency was relatively lower with higher concentration of nylon salt

especially under low temperature and high water content. Appropriately increase the reaction temperature or reduce the initial water content can accelerate the nylon salt dehydration reaction

thereby increasing the polymerization reaction efficiency. New nylon salt polymerization kinetics modeling method is not only applicable to nylon 66

but also to nylon 1212 and other salt solution polyme

rization systems.

关键词

Keywords

references

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