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混合聚烯烃热裂解动力学建模
引用本文:丁飞,张海荣,罗彩容,熊莲,陈新德.混合聚烯烃热裂解动力学建模[J].石油学报(石油加工),2012,28(5):821-826.
作者姓名:丁飞  张海荣  罗彩容  熊莲  陈新德
作者单位:1. 中国科学院 可再生能源与天然气水合物重点实验室,广东 广州 510640; 2. 中国科学院 广州能源研究所,广东 广州 510640; 3. 中国科学院 研究生院,北京 100049
基金项目:广东省自然科学基金(9451007006004075)资助
摘    要:通过混合聚烯烃在633.15~673.15K、初始反应压力6.325kPa条件下的釜式热裂解实验,考察了反应温度和反应时间对裂解反应生成的产物分布的影响,并建立了四集总动力学模型,对聚烯烃制备高附加值产品的最佳工艺条件进行了优化。结果表明,利用该模型计算得到的产物分布与实验数据吻合较好,误差较小;混合聚烯烃裂解的总表观活化能为110.4 kJ/mol,指前因子(A)为2.69×107 min-1,塑料添加剂的存在一定程度上降低了反应活化能。在653.15 K下混合聚烯烃裂解反应40 min,重组分收率最高,达到57.2%;在673.15 K下混合聚烯烃裂解反应120 min,中间组分收率最高,达到57.0%。这一研究结果可为废弃塑料热裂解制备高附加值产品提供理论指导。

关 键 词:废弃塑料  聚烯烃  添加剂  热裂解  高附加值产品  动力学模型  
收稿时间:2011-09-06

Dynamics Modeling of Pyrolysis of Mixed Polyolefin
DING Fei,ZHANG Hairong,LUO Cairong,XIONG Lian,CHEN Xinde.Dynamics Modeling of Pyrolysis of Mixed Polyolefin[J].Acta Petrolei Sinica (Petroleum Processing Section),2012,28(5):821-826.
Authors:DING Fei  ZHANG Hairong  LUO Cairong  XIONG Lian  CHEN Xinde
Affiliation:1. Key Laboratory of Renewable Energy and Gas Hydrate, Chinese Academy of Sciences, Guangzhou 510640, China; 2. Guangzhou Institute of Energy Conversion, Chinese Academy of Sciences ,Guangzhou 510640, China; 3. Graduate University, Chinese Academy of Sciences, Beijing 100049, China
Abstract:Pyrolysis of mixed polyolefin was carried out in an autoclave under the reaction temperatures of 633.15~673.15K, initial pressure of 6.325kPa. The influences of reaction temperature and time on the product distribution of polyolefin pyrolysis were investigated. A four-lump kinetic model was also established. Finally, the optimum process conditions were found to obtain maximum yield of value-added products. The results showed that the four-lump kinetic model fit for the pyrolysis reaction of polyolefin. The results calculated by the kinetic model agreed well with experimental data. The overall activation energy and pre-exponential factor was estimated to be 110.4 kJ/mol and 2.69×107 min-1 for the pyrolysis of mixed polyolefin. The apparent activation energy reduced in the presence of plastic additives. The heavy fractions yield could reach its highest value of 57.2%, when the mixed polyolefin was pyrolyzed at 653.15 K for 40 min, and the middle distillate yield was up 57.0%, when the mixed polyolefin was pyrolyzed for 120 min at 673.15 K. The conclusions can provide theoretic direction for conversion of waste plastic to value-added products.
Keywords:waste plastic  polyolefin  additives  pyrolysis  value-added products  kinetics model
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