萃取精馏及进展

萃取精馏是一种特殊精馏方法 ,适用于近沸点物系和共沸物的分离。萃取精馏按操作方式可分为连续萃取精馏和间歇萃取精馏 ,间歇萃取精馏是近年发展起来的新的萃取精馏方法。萃取精馏的关键是溶剂的选择 ,以往萃取精馏采用的溶剂是单一溶剂 ,近年来人们开始研究使用混合溶剂 ,取得了良好效果     

分批间歇萃取精馏技术的进展

对分批问歇萃取精馏技术和进展进行了评述，从分批问歇萃取精馏的操作方式、操作可行性、操作优化等几方面介绍了分批间歇萃取精馏的研究情况，指出存在问题和发展方向。     

间歇萃取精馏技术的进展

对间歇萃取精馏分离技术和进展进行了评述,主要从萃取精馏溶剂选择,操作方式,新型塔设备的研究,操作优化及过程模拟等几个方面,介绍了国内外关于间歇萃取精馏新兴分离技术的最新研究动态,最后指出了萃取精馏技术目前存在的问题和今后发展的方向。     

双再沸器间歇萃取精馏及模拟

本文提出了具有双再沸器的间歇萃取精馏新方法。实验选用乙二醇作为溶剂分离乙醇-水共沸物．结果表明,双再沸器间歇精馏具有再沸器温度稳定、操作简便、节省操作时间、收率提高等优点。为了更深入的研究间歇萃取精馏,本文建立了描述间歇萃取精馏的平衡级恒摩尔持液模型,并对此数学模型求解,通过模拟结果与实验结果的对比分析了塔顶与塔底浓度和温度的变化、溶剂流率等操作参数对实验的影响。     

带塔底储罐的间歇萃取精馏的实验研究

提出了带塔底储罐的间歇萃取精馏操作方式.新操作方式使精馏过程中加入的溶剂及塔内回流液直接流入塔底储罐,不再返回塔釜.以乙二醇为溶剂分离乙醇–水共沸物的实验研究表明,新操作方式克服了普通间歇萃取精馏塔釜体积庞大的缺陷,同时具有塔釜温度稳定、加热容易控制、收率提高等优点.     

带有中间储罐的间歇萃取精馏的模拟研究

本文提出了带有中间储罐塔间歇萃取精馏过程计算模型,将中间罐看成一块理论板,萃取剂看成第三组份进行建模,利用调节因子和泡点法相结合对整个塔进行迭代计算,经实例模拟表明,本模型只需较简单的赋初值,能以较快的速度收敛,本模型对带有中间储罐间歇萃取精馏操作及模拟具有一定的指导作用。     

间歇萃取精馏技术的研究进展

对间歇萃取精馏分离技术和进展进行了评述,主要从萃取精馏的溶剂选择与设计、模拟及优化、操作参数对分离过程影响及萃取精馏塔设备等几个方面,介绍了国内外关于间歇萃取精馏新兴分离技术的最新研究动态,最后指出了萃取精馏技术目前存在的问题和今后发展的方向。     

化工生产废液中四氢呋喃的回收

1引言 间歇精馏以其操作灵活、投资少并适合分离热敏性物料等特点而被广泛应用于现代化工生产。萃取精馏是一种常用的特殊精馏方法,通过加入高沸点的第三组分（萃取剂）来改变原混合物的相对挥发度而使共沸物或近沸点物系分离。20世纪80年代Berg提出了间歇萃取精馏操作方式,它同时具备了间歇精馏的灵活性、经济性与萃取精馏的实用性,特别适用于化工、制药、石油深加工等行业中普通精馏无法完成的相对挥发度小的物系的分离,兼有学术研究和实际应用价值。     

间歇萃取精馏过程模拟计算

提出了一种可用于间歇萃取精馏过程模拟计算的快捷模型－准稳态模型，并对该方法的数学模型进行了推导。用此方法对间歇萃取精馏过程中塔顶、塔釜浓度，各塔板温度随时间的变化进行模拟，其结果与实验值吻合较好。它具有计算精度高、计算速度快等优点。     

伴有简单蒸馏的间歇萃取精馏方法研究

提出了伴有简单蒸馏的间歇萃取精馏操作方式。在新操作方式中，混有溶剂的塔内液相不流回塔釜，而是流入塔底简单蒸馏釜，再经简单蒸馏的汽相返回塔釜，而富含溶剂的液相留在简单蒸馏釜中。以乙二醇作溶剂分离乙醇-水物系统为例的实验研究表明：新的操作方式具有塔釜温度稳定、溶剂回收简便、操作时间短和操作弹性大等优点。     

拟稳态模型用于间歇萃取精馏的数值模拟

Batch extractive distillation (BED) is a special method used in the distillation process by adding a solvent into the batch distillation column to alter the relative volatility of the components and improve the separation. A comprehensive design and simulation method is required due to the complexity of BED. In this study, a quasi-steady-state model for BED is proposed, the derivation and solution of the model are presented. This shortcut model can be used to simulate the composition and temperature of the reboiler, the top and other plates of the column in a batch extractive distillation operation. The calculated values are in good agreement with the experi-mental data. The results show that the quasi-steady-state model is a practical method because of some advantages such as high precision and fast calculation.     

分批萃取精馏回收无水乙醇的新工艺

针对分批萃取精馏法回收无水乙醇原有工艺流程中存在的问题,提出了优化方案。在原有流程的基础上,添加了一个溶剂回收釜,塔的下段液相流体直接流入溶剂回收釜。结果使得塔釜的温度变化降低,加热容易控制,操作时间变短。此方案对分批萃取精馏法回收无水乙醇的工艺改造有参考价值。     

Extractive distillation: Advances in conceptual design,solvent selection,and separation strategies

Extractive distillation(ED) is one of the most promising approaches for the separation of the azeotropic or closeboiling mixtures in the chemical industry. The purpose of this paper is to provide a broad overview of the recent development of key aspects in the ED process involving conceptual design, solvent selection, and separation strategies. To obtain the minimum entrainer feed flow rate and reflux ratio for the ED process, the conceptual design of azeotropic mixture separation based on a topological analysis via thermodynamic feasibility insights involving residue curve maps, univolatility lines, and unidistribution curves is presented. The method is applicable to arbitrary multicomponent mixtures and allows direct screening of design alternatives. The determination of a suitable solvent is one of the key steps to ensure an effective and economical ED process. Candidate entrainers can be obtained from heuristics or literature studies while computer aided molecular design(CAMD) has superiority in efficiency and reliability. To achieve optimized extractive distillation systems, a brief review of evaluation method for both entrainer design and selection through CAMD is presented. Extractive distillation can be operated either in continuous extractive distillation(CED) or batch extractive distillation(BED), and both modes have been well-studied depending on the advantages in flexibility and low capital costs. To improve the energy efficiency, several configurations and technological alternatives can be used for both CED and BED depending on strategies and main azeotropic feeds. The challenge and chance of the further ED development involving screening the best potential solvents and exploring the energy-intensive separation strategies are discussed aiming at promoting the industrial application of this environmentally friendly separation technique.     

Comparison of diester waste treatment by conventional andbipolar electrodialysis

Diester manufacturing plants produce large quantities of glycerol solutions. Their economic development requiressodium sulfate elimination to obtain glycerol rates over 80% of the initial content. Conventional electrodialysis (ED) and bipolar electrodialysis (BED) were investigated for their performances in the demineralisation of effluents. Results indicate that both ED and BED achieve the demineralisation objective with a global loss below 2.5% of the initial glycerol. Salt fluxes are twice as high with a bipolar membrane, bipolar membranes having however a lower efficiency. Hence energetic consumption is higher for BED. This technique also leads to the production of alkali and acid solutions which are useful to the diester process. The glycerol content of the solutions acts, via its viscosity, on the energetic cost of fluid pumping and on energetic efficiency. Therefore, ED or BED has to be used before the preconcentration of the solution.     

Design and Control Comparison of Alternative Separation Methods for n‐Heptane/Isobutanol

The binary mixture of n‐heptane and isobutanol forms an azeotrope at atmospheric pressure, with a composition of 66.9 mol % n‐heptane and a temperature of 364 K. Several methods of separation are possible. This study compares the steady‐state economics and the dynamic controllability of three alternative separation techniques: a two‐column extractive distillation process, a two‐column pressure‐swing distillation process, and a single column with a refrigerated condenser.     

分子蒸馏过程模型化研究进展

介绍了分子蒸馏基本原理和常用分子蒸馏设备 ,系统地对分子蒸馏过程模型化的研究进展情况进行了叙述 ,重点介绍了蒸发系数法、液体内部传质传热和蒸馏区惰性气体压力对分子蒸馏的影响等方面的研究结果 ,并对其进行了评述 ,同时对分子蒸馏过程研究的进一步发展提出了一些展望。     

Comparison of continuous homogenous azeotropic and pressure-swing distillation for a minimum azeotropic system ethyl acetate/n-hexane separation

Continuous homogenous azeotropic distillation (CHAD) and pressure-swing distillation (PSD) are explored to separate a minimum-boiling azeotropic system of ethyl acetate and n-hexane. The CHAD process with acetone as the entrainer and the PSD process with the pressures of 0.1 MPa and 0.6 MPa in two columns are designed and simulated by Aspen Plus. The operating conditions of the two processes are optimized via a sequential modular approach to obtain the minimum total annual cost (TAC). The computational results show that the partially heat integrated pressure-swing distillation (HIPSD) has reduced in the energy cost and TAC by 40.79% and 35.94%, respectively, than the conventional PSD, and has more greatly reduced the energy cost and TAC by 62.61% and 49.26% respectively compared with the CHAD process. The comparison of CHAD process and partially HIPSD process illustrates that the partially HIPSD has more advantages in averting the product pollution, energy saving, and economy.     

反应蒸馏塔中固体催化剂的装填结构

反应蒸馏是集化学反应与蒸馏分离两个过程于一体的新化工单元过程 ,反应蒸馏塔中固体催化剂的装填结构既要满足汽液两相对流流动的需要 ,又要使反应介质与催化剂能够良好接触。简述了对反应蒸馏塔中固体催化剂装填结构的基本要求 ,分类介绍了国内外开发的有特色与应用前景的催化剂装填结构的特点、局限性与应用范围 ,指出了开发新型催化剂装填结构的必要性     

Design of entrainer-enhanced reactive distillation for the synthesis of butyl cellosolve acetate

An innovative entrainer-enhanced reactive distillation (RD) process is presented, which aims to the production of high-purity butyl cellosolve acetate from butyl cellosolve and acetic acid via an esterification reaction. This entrainer-enhanced RD process can procure technical advantages from both heterogeneous azeotropic distillation and RD. Solvents such as cyclohexane, ethylene dichloride, toluene, and octane are considered as candidates in this esterification RD process. The function of entrainers is to simplify the separation between water and acetic acid. For this purpose, the proper entrainer to use is thus evaluated based on its mutual solubility with water in two liquid phases. Simulation results reveal that total annual cost can be substantially reduced when cyclohexane, toluene, and octane are used as entrainers in the RD column. The octane-enhanced RD provides the most economical design in this studied case.