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使用多相催化剂对乙醇酸进行反应精馏:实验研究与过程模拟

Reactive Distillation of Glycolic Acid Using Heterogeneous Catalysts: Experimental Studies and Process Simulation.

作者信息

Mutschler Carole, Aparicio Juliana, Mokbel Ilham, Capron Mickaël, Fongarland Pascal, Araque Marcia, Nikitine Clémence

机构信息

CP2M, UMR CNRS 5128, University Lyon 1, CPE Lyon, Villeurbanne, France.

University Lille, CNRS, Centrale Lille, ENSCL, University Artois, UMR 8181 - UCCS - Unité de Catalyse et Chimie du Solide, Lille, France.

出版信息

Front Chem. 2022 Jun 15;10:909380. doi: 10.3389/fchem.2022.909380. eCollection 2022.

Abstract

The glycerol oxidation reaction was developed leading to selective catalysts and optimum conditions for the production of carboxylic acids such as glycolic acid. However, carboxylic acids are produced in highly diluted mixtures, challenging the recovery and purification, and resulting in high production costs, polymerization, and thermal degradation of some of the products. The protection of the acid function by esterification reaction is one of the most promising alternatives through reactive distillation (RD); this technique allows simultaneously the recovery of carboxylic acids and the elimination of most part of the water. The reactive distillation, experimental and simulation, of glycolic acid was performed, based on kinetic and thermodynamic models developed. For the thermodynamic model, binary parameters of the missing couples were determined experimentally, and the non-random two-liquid (NRTL) model was selected as the most suitable to represent the binary behavior. The kinetic study of the esterification in the presence of homogeneous and heterogeneous catalysis concluded that the heterogeneous reaction can be accurately described either by a pseudo-homogeneous model or the Langmuir-Hinshelwood (L-H) adsorption model. Reactive distillation was conducted in a distillation column filled with random packing sulfonated ion-exchange resin, Nafion NR50, or with extruded TiO-Wo. The conversion rate of glycolic acid in reactive distillation increases from 14% without catalyst to 30% and 36% using Nafion NR50 and TiO-Wo, respectively. As opposed to the batch reactor study, the conversion rate of glycolic acid was better with TiO-Wo than with sulfonated ion-exchange resin. The better performance was related to an increase in the hydrodynamics inside the column. Tests using water in the feed confirm the hypothesis by increasing the conversion rate because of the decrease in the mass transfer resistance by reducing the average diffusion coefficient. The simulation of the reactive distillation column with ProSim Plus showed that the yield of the ester increased operating at a low feed rate with reactive stripping. In the presence of water in the feed, nonreactive stages are required, including an enrichment region to separate water vapor.

摘要

开发了甘油氧化反应,得到了用于生产乙醇酸等羧酸的选择性催化剂和最佳条件。然而,羧酸是在高度稀释的混合物中产生的,这对回收和纯化提出了挑战,导致生产成本高昂、一些产品发生聚合和热降解。通过反应蒸馏(RD)对酸官能团进行酯化反应保护是最有前景的替代方法之一;该技术可以同时回收羧酸并去除大部分水。基于所开发的动力学和热力学模型,对乙醇酸进行了反应蒸馏实验和模拟。对于热力学模型,通过实验确定了缺失二元体系的二元参数,并选择非随机双液(NRTL)模型作为最适合描述二元行为的模型。对均相和非均相催化下酯化反应的动力学研究得出结论,非均相反应可以用拟均相模型或朗缪尔-欣谢尔伍德(L-H)吸附模型准确描述。反应蒸馏在填充有散装磺化离子交换树脂Nafion NR50或挤出型TiO-Wo的蒸馏塔中进行。在反应蒸馏中,乙醇酸的转化率从无催化剂时的14%分别提高到使用Nafion NR50和TiO-Wo时的30%和36%。与间歇反应器研究不同,使用TiO-Wo时乙醇酸的转化率比磺化离子交换树脂更好。更好的性能与塔内流体动力学的增加有关。进料中用水进行的测试证实了这一假设,即由于通过降低平均扩散系数降低了传质阻力,从而提高了转化率。用ProSim Plus对反应蒸馏塔进行模拟表明,在低进料速率下进行反应汽提操作时,酯的产率会提高。在进料中有水的情况下,需要非反应阶段,包括一个用于分离水蒸气的富集区。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06f6/9240659/5d50fda37c51/fchem-10-909380-g001.jpg

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