Choice of suitable entrainer in heteroazeotropic batch distillation system for acetic acid dehydration

Mixture containing acetic acid and water does not form azeotrope. However, because of tangent pinch on the pure water end, it is customary in industry to add an entrainer into this mixture to aid the separation via heterogeneous azeotropic distillation. When the production scale is relatively small, it is more beneficial to run the acetic acid dehydration in batch mode. In Chien et al. [Chien, I. L., K. L. Zeng, H. Y. Chao, and J. H. Liu, “Design and Control of Acetic Acid Dehydration System via Heterogeneous Azeotropic Distillation,” Chemical Engineering Science, 59, 4547 (2004)], a suitable entrainer for acetic acid dehydration operating in continuous mode was found to be iso-butyl acetate. This paper demonstrates that although iso-butyl acetate is a good entrainer for continuous heterogeneous azeotropic distillation system, it is not suitable in heteroazeotropic batch system for acetic acid dehydration. Instead, the performances of two other acetates are compared for the suggestion of better entrainer in batch operation. An extremely simple batch operating sequence for acetic acid dehydration will be demonstrated via dynamic simulation. The proposed batch operation is very robust in terms of the particular values chosen for the operating variables. This proposed batch operation gives very similar separation performance comparing to a multivessel operation and requires less process, instrumentation, and control equipments.     

Heterogeneous extractive batch distillation of chloroform-methanol-water: Feasibility and experiments

A novel heterogeneous extractive distillation process is considered for separating the azeotropic mixture chloroform-methanol in a batch rectifying column, including for the first time an experimental validation of the process. Heterogeneous heavy entrainer water is selected inducing an unstable ternary heteroazeotrope and a saddle binary heteroazeotrope with chloroform (ternary diagram class 2.1-2b). Unlike the well-known heterogeneous azeotropic distillation process and thanks to continuous water feeding at the column top, the saddle binary heteroazeotrope chloroform-water is obtained at the column top, condensed and further split into the liquid-liquid decanter where the chloroform-rich phase is drawn as distillate. First, feasibility analysis is carried out by using a simplified differential model in the extractive section for determining the proper range of the entrainer flowrate and the reflux ratio. The operating conditions and reflux policy are validated by rigorous simulation with ProSim Batch Column^® where technical features of a bench scale distillation column have been described. Six reproducible experiments are run in the bench scale column matching the simulated operating conditions with two sequentially increasing reflux ratio values. Simulation and experiments agree well. With an average molar purity higher than 99%, more than 85% of recovery yield was obtained for chloroform and methanol.     

New double column system for heteroazeotropic batch distillation

A new double column system (DCS) operated in closed mode is suggested for heterogeneous batch distillation. This configuration is investigated by feasibility studies based on the assumption of maximal separation and is compared with the traditional batch rectifier (BR). We study the configurations also by dynamic simulation based on a detailed model using a professional simulator. For the new configuration the minimal duration of the process is determined. The influence of the most important operational parameters is studied. The calculations and the simulations are performed for a binary (n-butanol–water) and for a ternary heteroazeotropic mixture (isopropanol–water + benzene as entrainer). One of the advantages of the DCS is that distillation of binary and ternary systems is performed in only one step. Furthermore the recovery of components is usually higher and the amount of byproducts is lower.     

Design and control of acetic acid dehydration system via heterogeneous azeotropic distillation

Acetic acid dehydration is an important operation in the production of aromatic acid, such as terephthalic acid or in the manufacture of cellulose acetate. Although acetic acid and water does not form azeotrope, but using simple distillation to separate these two components is not practical. The reason is because the system has tangent pinch on the pure water end, thus it is more customary in industry to use an entrainer via a heterogeneous azeotropic distillation column system for the separation. In this study, a suitable entrainer is selected from three candidate acetates through rigorous steady-state simulation of this system. Optimum process design and operating condition are determined to keep high-purity bottom acetic acid composition and also keep a small acetic acid loss through top aqueous draw. Furthermore, the overall control strategy of this column system is proposed to hold both bottom and top product specifications in spite of feed rate and feed composition load disturbances. The proposed overall control strategy is very simple requiring only one tray temperature control loop inside the heterogeneous azeotropic column.     

Influence of entrainer recycle for batch heteroazeotropic distillation

Dehydration of isopropanol applying batch heteroazeotropic distillation with toluene as entrainer (E) is investigated. The composition of the feed is near to that of the isopropanol (A)-water (B) azeotrope. The effects of recycling the entrainer and the off-cut are studied by dynamic simulation with a professional flow-sheet simulator. Three consecutive batches (one production cycle) is studied. Both operational modes (Mode I: decantation after distillation and Mode II: decantation during distillation) are simulated. For Mode II, calculations are performed both for Strategy A (distillate from the aqueous (E-lean) phase only) and Strategy B (partial withdrawal of the organic (Erich phase), as well). The E-rich phase, the final column hold-up and the off-cut (Mode II only) are recycled to the next batch. The influence of the following parameters are determined: quantity of entrainer, reflux ratios of the steps. The variations caused by the recycling in the 2^nd and 3^rd batches are also shown. The best results (lowest specific energy demand and highest recovery of A) are obtained by Mode II, Strategy A. Recycling increases the recovery, and drastically diminishes the entrainer consumption. However, it makes the production slower and decreases the quantity of fresh feed that can be processed.

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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.     

结合图论和基团贡献法的非均相共沸精馏挟带剂设计

非均相共沸精馏挟带剂的计算机辅助分子设计(CAMD)由分子合成、分子筛选及分子确认3个环节递进构成。在分子合成环节,预选基团,限定合成分子的基团总数及类型,基于图论原理实现由基团到分子的自动合成。在分子筛选环节,依据基础物性筛选指标形成基础分子库,输入待分离物系,采用非均相共沸物形成判据筛选出若干候选分子。在分子确认环节,由非均相共沸温度及组成、挟带剂的汽化热等参数组成模糊综合评判函数,实现分子排序,从而输出一组较优挟带剂。以乙酸-水物系、乙腈-乙酸乙酯物系为例,得到了相应设计结果,与文献结果进行了对比。研究表明该方法及所编程序具备可靠实用性,可为近沸程及共沸混合物分离过程的开发与设计提供先导性支持。     

Operation and control of batch extractive distillation for the separation of mixtures with minimum-boiling azeotrope

Batch distillation is commonly used in the fine chemicals, specialty polymer, biochemical, pharmaceutical, and food industries. For separating mixtures with minimum-boiling azeotrope, a heavy entrainer is frequently added to the top section of the batch column to aid in the separation. This process is called batch extractive distillation. Most of the papers in open literature have only studied the first operating step of the batch extractive distillation which is the recovery of the light component without mentioning the later steps for the recovery of the other component and entrainer. In this paper, two real chemical systems, one separating acetone and methanol using water as entrainer and the other separating isopropyl alcohol (IPA) and water using dimethyl sulfoxide (DMSO) as entrainer, are studied for the feasible operation of the complete batch distillation sequence. The operating variables, including the pre-load amount with the mixture, continuous feed rate of the entrainer, and reflux ratio at each operating step are determined in the operating sequence. The constant reflux ratio and constant entrainer feed rate operating policy and another policy to allow these two operating variables to be varied will be compared in order to further improve the batch operation. All dynamic simulations that are performed directly mimic industrial situations from an empty column using a rigorous dynamic simulator, Aspen Dynamics™.     

Generalised method for the determination of heterogeneous batch distillation regions

A new, general method for the calculation of residue curves and for the determination of batch distillation regions of heteroazeotropic distillation is suggested. The method proposed, which means the extension of the method of Pham and Doherty, takes into consideration the possibility of the withdrawal of any fraction of either liquid phase from the decanter as distillate. The simplified and rigorous simulation calculations were carried out for the mixtures dichloromethane-acetone (low α) + water (heavy, selective, heterogeneous entrainer), water-ethylenediamine (maximum azeotrope) + benzene (light, selective, heterogeneous entrainer) and isopropanol-water (minimum azeotrope) + benzene (light, non-selective, heterogeneous entrainer). The new method gives the right sequence of the cuts for all operation modes and strategies of heterogeneous batch distillation.     

A semicontinuous approach for heterogeneous azeotropic distillation processes

The separation of azeotropes has substantial energy and investment costs, and the available methods require high capital costs for reconstruction of process plants. As an alternative, a semicontinuous configuration that utilizes an existing plant with minor modifications has been explored. In this paper, a semicontinuous, heterogeneous azeotropic distillation process is proposed and acetic acid dehydration process is used as a case study. To carry out the simulation work, Aspen HYSYS^® simulation software is used along with MATLAB^® and an interface program to handle the mode-transition of the semicontinuous process. Sensitivity analyses on operating parameters are performed to identify the process limits. Comparisons are made to conventional heterogeneous azeotropic distillation, and dividing-wall distillation column on the annual cost. The results proved that the semicontinuous system is the best setup in terms of total annual costs and energy requirements.     

Flowsheet synthesis and complex distillation column design for separating ternary heterogeneous azeotropic mixtures

The boundary value method for design of distillation columns separating ternary heterogeneous azeotropic mixtures is extended to include complex configurations, i.e. columns with integrated decanters and with multiple heterogeneous stages; double-feed columns; columns with intermediate decanters. The methods can be used for establishing product feasibility in a column and evaluating a column design in terms of cost. Multiple feasible designs can be generated for a given set of product specifications, according to the reflux ratio, number of heterogeneous stages and liquid phase ratio; these designs may be evaluated with respect to operating and equipment costs. Case studies illustrate the design method.An algorithmic approach is presented for synthesising novel sequences for separating, by distillation and decanting, ternary heterogeneous azeotropic mixtures. Existing synthesis procedures that consider only simple single-feed columns with decanters and integrated decanters are extended to include more industrially relevant options such as columns with several heterogeneous stages, double-feed columns, columns with intermediate decanters, and those accepting a heterogeneous liquid feed. With these advanced column configurations included in the synthesis method, a wider range of sequences may be considered systematically, allowing sequences that are more economically attractive than conventional designs to be identified. A case study illustrates the approach.     

MINLP optimization of a heterogeneous azeotropic distillation process: Separation of ethanol and water with cyclohexane as an entrainer

Heterogeneous distillation processes are widely used in industry for the separation of azeotropic and close-boiling mixtures. This paper addresses the optimization of a heterogeneous distillation process for the separation of an azeotropic ethanol/water mixture using cyclohexane as an entrainer. Starting from a given process superstructure a MINLP problem is set up to consider continuous as well as discrete decision variables such as the feed locations and the number of stages of the distillation columns. A modified Generalized Benders Decomposition algorithm to account for non-convexities of the model equations solves the MINLP problem. The algorithm can be attached via Visual Basic for Applications (VBA) to any commercial process simulator with NLP and VBA capabilities. Various optimization runs show that the algorithm is easily applicable and returns solutions independent of the initial values.     

Dynamic parameter estimation and optimization for batch distillation

This work reviews a well-known methodology for batch distillation modeling, estimation, and optimization but adds a new case study with experimental validation. Use of nonlinear statistics and a sensitivity analysis provides valuable insight for model validation and optimization verification for batch columns. The application is a simple, batch column with a binary methanol–ethanol mixture. Dynamic parameter estimation with an ℓ₁-norm error, nonlinear confidence intervals, ranking of observable parameters, and efficient sensitivity analysis are used to refine the model and find the best parameter estimates for dynamic optimization implementation. The statistical and sensitivity analyses indicated there are only a subset of parameters that are observable. For the batch column, the optimized production rate increases by 14% while maintaining product purity requirements.     

用离子液体作催化剂和夹带剂时在反应萃取精馏塔中乙酸甲酯和正丁醇酯交换反应的模拟

A new reactive and extractive distillation process with ionic liquids as entrainer and catalyst (RED-IL) was proposed to produce methanol and n-butyl acetate by transesterification reaction of methyl acetate with n-butanol. The RED-IL process was simulated via a rigorous model, and high purity products of methanol and n-butyl acetate can be obtained in such a process. The effects of reflux ratio, feed mode, holdup, feed location, entrainer ratio and catalyst concentration on RED-IL process were investigated. The conversion of methyl acetate and purities of products increase with the holdup in column, entrainer ratio and catalyst content. An optimal reflux ratio exists in RED-IL process. Comparing to the mixed-feed mode, the segregated-feed mode is more effective, in which the optimal feed locations of reactants exist.     

Modelling and simulation of a hybrid process (pervaporation–distillation) for the separation of azeotropic mixtures of alcohol–ether

This work reports the modelling and simulation of a hybrid process, based on the combination of distillation and pervaporation, for the separation of azeotropic mixtures of alcohol–ether. After having selected the separation of methanol‐2‐metoxi‐2,2‐dimethyl ethane (ETHER) as a motivating example the mathematical modelling of the distillation column was achieved and used together with a mass transfer model previously reported for the pervaporation operation in order to simulate the behaviour of the hybrid process for different compositions of the feed stream (case 1: 3.2 wt% methanol, 55.4 wt% C₄, 41.4 wt% ETHER, and case 2: 5.2 wt% methanol, 42 wt% C₄, 52.8 wt% ETHER). Simulation tasks were carried out with the process modelling system gPROMS and the results of alternative process configurations that result from the relative location of the separation technologies have been compared on the basis of the required membrane area. Finally, the design of the pervaporation unit including the overall processing costs is reported. Copyright © 2001 Society of Chemical Industry     

Short-cut methods for the optimal design of simple and complex distillation columns

New short-cut methods providing optimal design parameters for distillation columns with simple and complex configurations including two-feed and one-feed-one-side-stream columns are presented. The methods assume constant relative volatilities and constant molar flow rates within each distillation section. The design equations are based on the Underwood equations for the calculation of minimum reflux (reboil) ratio, the analytical formulations of the distillation line, the Eigenfunction and the number of theoretical stages for each mass transfer section of the column. Furthermore, the geometrical properties of a given separation are considered. Optimization algorithms based on the minimization of the total number of theoretical stages of the column with taking into account the mass balance at each feed section have been elaborated. In comparison to the boundary value method the new short-cut methods require a minimum number of specifications; they do not need any graphical support, and provide a lower total number of theoretical stages particularly for complex configurations. The new short-cut methods have been extended to the design of columns separating azeotropic mixtures by approximating the latter by appropriate pseudo-ideal mixtures. Several separation examples for azeotropic mixtures, including different types of splits as well as columns with simple and complex configurations were tested and show a very good agreement with the simulation results obtained with Radfrac (Aspenplus).     

Hybrid separations combining distillation and organic solvent nanofiltration for separation of wide boiling mixtures

Membrane assisted hybrid separations offer tremendous potential for process intensification which aims at increasing resource efficiency as well as decreasing operating and capital costs. Design of such processes is challenging due to large number of degrees of freedom but also due to large experimental effort necessary for membrane screening and for characterising membranes in whole operating range. To address these issues, this paper elaborates a four-step design method for combination of organic solvent nanofiltration (OSN) and distillation in a hybrid separation of wide boiling mixtures. The design method is applied in a case study which is the separation of small amounts of heavy boiler from a mixture containing a mid- and a light-boiler. In the first step, different process options are generated based on heuristics and engineering judgement and screened for feasibility. In the second step, the options are evaluated based on quantitative metrics using rigorous models. In this step the unknown key parameters are identified, and their influences on the process performance are quantified in a detailed a priori process analysis. If hybrid separations with OSN show to be promising when compared to stand-alone distillation, experiments are conducted to (i) identify the best membrane for the operating window in which the hybrid process operates and (ii) to perform model validation and parameterisation in the third step. In the last (fourth) step, an optimisation is performed to identify the best (cost optimal) process using the experimental data gained in step three.