电工技术学报  2025, Vol. 40 Issue (10): 3082-3096    DOI: 10.19595/j.cnki.1000-6753.tces.240616
电工材料 |
基于ReaxFF的产气材料热解及动力学分析
汪倩1, 赵婉萌1, 曹伟东2, 尚毅1
1.西安理工大学理学院 西安 710048;
2.电工材料电气绝缘全国重点实验室(西安交通大学) 西安 710049
Analyzing the Pyrolysis Kinetics and Pyrolysis Gases of Gassing Materials Using ReaxFF
Wang Qian1, Zhao Wanmeng1, Cao Weidong2, Shang Yi1
1. School of Sciences Xi’an University of Technology Xi’an 710048 China ;
2. State Key Laboratory of Electrical Insulation and Power Equipment Xi’an Jiaotong University Xi’an 710049 China;
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摘要 可再生能源的快速发展对电力系统中直流断路器的开断能力提出了重大挑战,基于产气材料的气吹灭弧技术可以极大地提高直流断路器的开断能力,然而目前并不清楚产气材料的宏观热解规律和微观热解机理。首先基于反应力场分子动力学分析了不同热解温度和不同热解速率下典型产气材料聚酰胺66(PA66)的微观热解机理,发现PA66的初始断键发生在与酰胺基团相邻的C—C键,H2和H2O是PA66的主要热解气体,对其产生过程进行了分析。然后进行了四种不同升温速率下的热解实验,并基于Flynn-Wall-Ozawa等转化率模型获取PA66的活化能均值为194.85 kJ/mol,与分子动力学模拟得到的活化能195.015 kJ/mol较为接近,同时采用热裂解-气谱/质谱实验分析了PA66的热解气体分布,在一定程度上验证了热解动力学计算方法的有效性。该研究为产气材料的宏观热解行为和微观热解机理提供了理论解释,同时为直流断路器用产气材料的性能评价提供了一定的方法基础。
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汪倩
赵婉萌
曹伟东
尚毅
关键词 聚酰胺66(PA66)热分解动力学活化能产气材料反应力场(ReaxFF)    
Abstract:In recent years, the rapid development of renewable energy has posed a significant challenge to the breaking capacity of DC circuit breakers in power systems. Gas-blowing arc extinguishing technology based on gassing materials can greatly enhance the breaking capacity of DC circuit breakers. However, the macroscopic and microscopic pyrolysis mechanisms of gassing materials are unclear.
Firstly, the micro-pyrolysis mechanism of typical gassing material polyamide 66 (PA66) at different pyrolysis temperatures and rates was analyzed based on the reactive force field (ReaxFF). The decomposition process of PA66 and the types and quantities of small molecule gases produced were discussed. It was found that the initial bond breaking of PA66 occurred in the C—C bond adjacent to the amide group. H2 and H2O were the main pyrolysis gases of PA66, and their production process was analyzed. The reaction rate of carbon-free small molecule gas at high temperatures accelerates, and the amount increases. The product amount with carbon atoms below four increases rapidly and decreases slightly after reaching a peak. The main reasons are the Diels-Alder reaction, C3/C4 reaction, and cyclization reaction in the unsaturated hydrocarbons in the product, which leads to the decrease of hydrocarbon molecules. The temperature increase aggravates the disintegration of the PA66 molecular chain and the formation of small molecular gas. The heating rate of the system affects the distribution of heat in the reaction system, thus affecting the formation of the product. The slower the heating rate of the system, the more conducive to the uniform distribution of heat in the reaction system. Additionally, the amount of carbon deposition during pyrolysis at 2 600 K was analyzed. Light tar was dominant, followed by heavy tar, with the least amount of coke.
Subsequently, pyrolysis experiments at four different heating rates were carried out. Based on the Flynn-Wall-Ozawa isoconversional model, the average activation energy of PA66 was 194.85 kJ/mol, which was very close to the activation energy of 195.015 kJ/mol obtained by molecular dynamics simulation. Additionally, the pyrolysis gas distribution of PA66 was analyzed by pyrolysis-gas chromatography/mass spectrometry (Py-GC/MS) experiments, which verified the accuracy and reliability of the pyrolysis kinetics calculation method. PA66 is suitable for the first-order reaction kinetic model, and the simulation data have high accuracy and reliability for the thermal decomposition reaction path and gas type of PA66 at the microscale.
Finally, simulation calculations and arcing experiments of three gas-producing materials, PA6, PA46, and PA66, were carried out. The gas generation rate and quantity changes during pyrolysis were observed, and the transient pressure changes during the arc-breaking experiment were analyzed. The order of transient pressure generated during the arcing process is PA6>PA46>PA66, consistent with the trend of the number of product gas molecules obtained by simulation calculation. The ReaxFF simulation results are confirmed and supplemented with the arc-breaking experiment, further verifying the reliability and accuracy of the research.
This paper offers a theoretical framework for understanding the macroscopic pyrolysis behavior and the microscopic pyrolysis mechanism of gassing materials. It contributes to a deep comprehension of material behavior under high-temperature and arc conditions, laying a methodological foundation for evaluating the performance of gassing materials in DC circuit breakers.
Key wordsPA66    thermal decomposition kinetics    activation energy    gassing materials    reactive force field (ReaxFF)   
收稿日期: 2024-04-22     
PACS: TM614  
基金资助:国家自然科学基金项目(52277163)和陕西省教育厅重点实验室项目(22JS025)资助
通讯作者: 赵婉萌 女,1999年生,硕士研究生,研究方向为基于分子动力学产气材料。E-mail:2220920070@stu.xaut.edu.cn   
作者简介: 汪倩 女,1981年生,教授,硕士生导师,研究方向为等离子体物理特性、电气设备设计及优化等。E-mail:qian.wang@xaut.edu.cn
引用本文:   
汪倩, 赵婉萌, 曹伟东, 尚毅. 基于ReaxFF的产气材料热解及动力学分析[J]. 电工技术学报, 2025, 40(10): 3082-3096. Wang Qian, Zhao Wanmeng, Cao Weidong, Shang Yi. Analyzing the Pyrolysis Kinetics and Pyrolysis Gases of Gassing Materials Using ReaxFF. Transactions of China Electrotechnical Society, 2025, 40(10): 3082-3096.
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