首页 | 本学科首页   官方微博 | 高级检索  
     

采用分离集成技术从碳十芳烃中提取均四甲苯
引用本文:周永兵,顾正桂,黄杰军,林军.采用分离集成技术从碳十芳烃中提取均四甲苯[J].石油化工,2009,38(10):1085.
作者姓名:周永兵  顾正桂  黄杰军  林军
作者单位:1. 南京师范大学南京萃取分离工程技术研究中心,江苏,南京,210097
2. 南京师范大学南京萃取分离工程技术研究中心,江苏,南京,210097;江苏沿江化工资源开发研究院,江苏,南京,210097
基金项目:中国石化扬子石油化工股份有限公司科研基金项目 
摘    要:采用萃取精馏和连续多级结晶相结合的分离集成技术从C_(10)芳烃中提取均四甲苯。选择甘油为萃取剂,考察实际塔板数、回流比、萃取剂与原料液的体积比(溶剂比)、进料量、结晶温度、结晶时间、抽滤时间等因素对分离均四甲苯的影响。萃取精馏条件:实际塔板数为106块、原料进料位置为第75块塔板、萃取剂进料位置为第5块塔板、溶剂比为1.0、回流比为4、原料进料量为2 mL/min,在此条件下,萃取塔顶馏分中均四甲苯的质量分数为42.7%,收率达到98.4%。连续多级结晶条件:结晶温度-6℃、结晶时间5 h、抽滤时间20 min,在此条件下,可将均四甲苯质量分数从42.7%提纯到99.18%,收率为90.95%。

关 键 词:碳十芳烃  均四甲苯  萃取精馏  多级结晶  分离集成技术

Separation of Durene from C_(10) Aromatics by Integrated Separation Technologies
Abstract:Separation of durene from C_(10) aromatics was carried out by integrated separation technologies of combining extractive distillation with multistage crystallization. Glycerol was selected as extractant. Effects of actual plate number, reflux ratio, volume ratio of extractant to feedstock (solvent ratio), feedstock flow rate, crystallization temperature, crystallization time and filtration time on separation of durene were investigated. Under optimal extractive distillation conditions: actual plate number 106 plate, feedstock position 75th plate, extractant feeding posion 5th plate, solvent ratio 1.0, reflux ratio 4 and feedstock flow rate 2 mL/min, mass fraction of durene in overhead and yield of durene can reach 42.7% and 98.4%, respectively. Under optimal multistage crystallization conditions: crystallization temperature -6 ℃, crystallization time 5 h and filtration time 20 min, mass fraction of durene crystal can reach farther from 42.7 % to 99.18 % and yield of durene is 90.95 %. The overall yield of the integrated separation technologies (by combining extraction distillation with multistage crystallization) is 89.49 %.
Keywords:C_(10) aromatics  durene  extractive distillation  multistage crystallization  integrated separation technology
本文献已被 万方数据 等数据库收录!
点击此处可从《石油化工》浏览原始摘要信息
点击此处可从《石油化工》下载全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号