基于能量目标的芳烃萃取精馏溶剂评价模型
详细信息    查看全文 | 推荐本文 |
  • 英文篇名:Solvent evaluation model base on energy consumption objective for aromatic extraction distillation units
  • 作者:汪勤 ; 张冰剑 ; 何畅 ; 陈清林
  • 英文作者:WANG Qin;ZHANG Bingjian;HE Chang;CHEN Qinglin;School of Chemical Engineering and Technology/Guangdong Engineering Technology Research Center for Petrochemical Energy Conservation, Sun Yat-sen University;
  • 关键词:萃取精馏 ; 热力学 ; 优化 ; 芳烃 ; 物性关联 ; 模型
  • 英文关键词:extractive-distillation;;thermodynamics;;optimization;;arene;;property correlation;;model
  • 中文刊名:HGSZ
  • 英文刊名:CIESC Journal
  • 机构:中山大学化学工程与技术学院/广东省石化过程节能工程技术研究中心;
  • 出版日期:2019-03-07 07:21
  • 出版单位:化工学报
  • 年:2019
  • 期:v.70
  • 基金:石化联合基金项目(U1462113)
  • 语种:中文;
  • 页:HGSZ201905017
  • 页数:8
  • CN:05
  • ISSN:11-1946/TQ
  • 分类号:161-168
摘要
以NRTL活度系数模型为基础,利用Aspen Plus对不同单组分萃取剂回收芳烃的萃取精馏装置进行了全流程模拟和工艺操作参数优化。综合考虑各操作变量及其关联,提出了基于局部耦合参数迭代优化的整体协同优化策略,在保证分离要求的条件下,以能耗为目标,对萃取精馏塔(EDC)、溶剂回收塔(ERC)的进料位置、ERC回流比等关键操作参数进行优化,建立过程能耗的物性关联模型。通过分析不同溶剂对芳烃萃取精馏过程能耗和分离效果的影响,提出了基于能耗目标的芳烃萃取精馏溶剂评价模型,结果表明影响芳烃萃取精馏过程能耗的关键物性为溶剂的分子量及常压沸点,所建立的过程能耗关联模型具有较高的关联性,其R2均大于0.9,可有效指导萃取精馏溶剂选择,为计算机辅助分子设计提供简化的目标函数。
        Based on the NRTL activity coefficient model, the whole process simulation and process parameters were optimized by using Aspen Plus for extractive distillation equipment for aromatics recovery from different single component extractants. With consideration of multiple variables and their interactions, a coordinative optimization strategy was further proposed from iterative optimization of local coupling parameters. At given separation specifications, energy consumption was optimized through adjusting critical operating parameters, such as the feed stages of extractive distillation column(EDC), the feed stage of entrainer recovery column(ERC) and the reflux ratio of ERC. An energy consumption model correlated with physical properties was presented based on the energy transfer rules. A solvent evaluation model based on the energy consumption objective for aromatic extraction distillation processes was put forward through the analysis of energy consumption and separation efficiency with different solvents. The results show that the molecular weight and boiling point of solvent are the pivotal factors influencing the energy consumption of aromatics extraction distillation units. There is a high correlation of the energy consumption model with the R2 value bigger than 0.9 which can guide the selection, evaluation and design of the extracting solvent for an aromatic ED process.
引文
[1]范景新,臧甲忠,于海斌,等.重芳烃轻质化研究进展[J].工业催化,2015,23(9):666-673.Fan J X,Zang J Z,Yu H B,et al.Research progress in conversion of heavy aromatics to light ones[J].Industrial Catalysis,2015,23(9):666-673.
    [2]段然,巩雁军,孔德嘉,等.轻烃芳构化催化剂的研究进展[J].石油学报(石油加工),2013,29(4):726-737.Duan R,Gong Y J,Kong D J,et al.Development of the catalyst for light paraffins aromatization[J].Acta Petrolei Sinica(Petroleum Processing Section),2013,29(4):726-737.
    [3]智研咨询集团.2018-2024年中国PX行业市场全景评估及投资潜力研究报告[EB/OL].北京:智妍咨询集团,2018[2018-10-05].http://www.chyxx.com/research/201802/613733.html.Zhiyan Consultative Group.Report of Panoramic Evaluation and Investment Potential Research for PX Industry Market in China from 2018 to 2024[EB/OL].Beijing:Zhiyan Consultative Group,2018[2018-10-05].http://www.chyxx.com/research/201802/613733.html.
    [4]Rahimpour M R,Jafari M,Iranshahi D.Progress in catalytic naphtha reforming process:a review[J].Appl.Energ.,2013,109(2):79-93.
    [5]韩凤山,林克之.世界芳烃生产技术的发展趋势[J].当代石油石化,2006,14(5):30-35.Han F S,Lin K Z.Development trends of aromatic production and technology in the world[J].Petroleum&Petrochemical Today,2006,14(5):30-35.
    [6]UOP.Aromatics[EB/OL].New York:Honeywell,2013[2018-10-05].https://www.uop.com/products/catalysts/aromatics/.
    [7]袁天聪.芳烃抽提工艺评析[J].石油化工设计,2003,20(4):5-8.Yuan T C.Summary of aromatics extraction process[J].Petrochemical Design,2003,20(4):5-8.
    [8]徐春明,杨朝合,林世雄.石油炼制工程[M].北京:石油工业出版社,2009:557-569.Xu C M,Yang Z H,Lin S X.Petroleum Refining Engineering[M].Beijing:Petroleum Industry Press,2009:557-569.
    [9]Ho T L,Fieser M,Fieser L.Fieser and Fieser’s Reagents for Organic Synthesis:Tetramethylene Sulfone(Sulfolane)[M].New York:John Wiley&Sons Inc.,2006:23.
    [10]Wittig R,Lohmann J,Gmehling J.Prediction of phase equilibria and excess properties for systems with sulfones[J].AIChE J.,2010,49(2):530-537.
    [11]Wang Z R,Huang L,Xia S Q,et al.Isobaric(vapour+liquid)equilibria for sulfolane with toluene,ethylbenzene,and isopropylbenzene at 101.33 kPa[J].J.Chem.Thermodyn.,2011,43(12):1865-1869.
    [12]Santiago R S,Aznar M.Liquid-liquid equilibria for quaternary mixtures of nonane+undecane+(benzene or toluene or mxylene)+sulfolane at 298.15 and 313.15 K[J].Fluid Phase Equilib.,2007,253(2):137-141.
    [13]Doulabi F S M,Mohsen-Nia M.Ternary liquid-liquid equilibria for systems of(sulfolane+toluene or chloronaphthalene+octane)[J].J.Chem.Eng.Data,2006,51(4):1431-1435.
    [14]Ko M,Im J,Sung J Y,et al.Liquid-liquid equilibria for the binary systems of sulfolane with alkanes[J].J.Chem.Eng.Data,2007,52(4):34-38.
    [15]Awwad A M,Al-Dujaili A H,Al-Haideri A M A.Liquid-liquid equilibria for pseudo-ternary systems:(sulfolane+2-ethoxyethanol)+octane+toluene at 293.15 K[J].Fluid Phase Equilib.,2008,270(1/2):10-14.
    [16]Wisniak J,Ortega J,Fernández L.A fresh look at the thermodynamic consistency of vapour-liquid equilibria data[J].J.Chem.Thermodyn.,2017,105:385-395.
    [17]汪勤,张冰剑,何畅,等.环丁砜萃取精馏过程模拟分析及工艺参数优化[J].化工学报,2017,68(5):1969-1976.Wang Q,Zhang B J,He C,et al.Process simulation and optimization of sulfolane extractive distillation[J].CIESC Journal,68(5):1969-1976.
    [18]Choi Y J,Cho K W,Cho B W,et al.Optimization of the sulfolane extraction plant based on modeling and simulation[J].J.Chem.Eng.,2000,17(6):712-718.
    [19]Li L M,Tu Y Q,Sun L Y,et al.Enhanced efficient extractive distillation by combining heat-integrated technology and intermediate heating[J].Ind.Eng.Chem.Res.,2016,55(32):8837-8847.
    [20]Berg L,Yeh A.Separation of m-xylene from o-xylene by extractive distillation[J].Chem.Eng.Commun.,2012,54(1-6):149-159.
    [21]Miyano Y,Henry S.Constants and infinite dilution activity coefficients of propane,propene,butane,isobutene,1-butene,isobutane,trans-2-butene and 1,3-butadiene in 1-propanol at T(260 to 340)K[J].J.Chem.Thermodyn.,2004,36(2):101-106.
    [22]Krummen M,Gmehling J.Measurement of activity coefficients at infinite dilution in N-methyl-2-pyrrolidone and N-formylmorpholine and their mixtures with water using the dilutor technique[J].Fluid Phase Equilib.,2004,215(2):283-294.
    [23]Lek-Utaiwana P,Suphanit B,Douglas P L,et al.Design of extractive distillation for the separation of close-boiling mixtures:solvent selection and column optimization[J].Comput.Chem.Eng.,2011,35(6):1088-1100.
    [24]Lyu Z,Zhou T,Chen L,et al.Simulation based ionic liquid screening for benzene-cyclohexane extractive separation[J].Chem.Eng.Sci.,2014,113(13):45-53.
    [25]董文威,傅吉全.苯-环己烷体系萃取精馏溶剂的计算机筛选[J].计算机与应用化学,2011,28(6):757-760.Dong W W,Fu J Q.Solvents selection by using of computer in extractive distillation separation for the system of benzenecyclohexane[J].Computers and Applied Chemistry,2011,28(6):757-760.
    [26]Chen B H,Lei Z G,Li Q S,et al.Application of CAMD in separating hydrocarbons by extractive distillation[J].AIChE J.,2010,51(12):3114-3121.
    [27]Qin J W,Ye Q,Xiong X J,et al.Control of benzene-cyclohexane separation system via extractive distillation using sulfolane as entrainer[J].Ind.Eng.Chem.Res.,2013,52(31):10754-10766.
    [28]Aniya V,De D,Satyavathi B.A comprehensive approach towards dehydration of tert-butyl alcohol by extractive distillation:entrainer selection,thermodynamic modeling and process optimization[J].Ind.Eng.Chem.Res.,2016,55(25):6982-6995.
    [29]Kossack S,Kraemer K,Gani R,et al.A systematic synthesis framework for extractive distillation processes[J].Chem.Eng.Res.Des.,2008,86(7):781-792.
    [30]刘家祺.传质分离过程[M].北京:高等教育出版社,2005:8-21.Liu J Q.Separation Process of Mass Transfer[M].Beijing:Higher Education Press,2005:8-21.
    [31]Henley E J,Seader J D,Roper D K.Separation Process Principles[M].New York:John Wiley&Sons Inc.,2002:46.
    [32]Renon H,Prausnitz J M.Local compositions in thermodynamic excess functions for liquid mixtures[J].AIChE J.,1968,14(1):135-144.

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700