Bryan A. Tiban-Anrango, Andrea N. Arias-Sánchez, Justo Lobato, Manuel A. Rodrigo
{"title":"Scale-up of a BTX electrochemically assisted reactive absorption","authors":"Bryan A. Tiban-Anrango, Andrea N. Arias-Sánchez, Justo Lobato, Manuel A. Rodrigo","doi":"10.1016/j.jelechem.2025.118998","DOIUrl":null,"url":null,"abstract":"<div><div>Electrochemical technologies have proven highly efficient in remediating polluted gas with benzene, toluene, and xylene (BTX). However, their scalability has yet to be explored to determine the best configurations to maintain optimal removals and energetic efficiencies. Here, we report a straightforward scale-up of an electro-absorption process that combines the absorption of BTX in 0.05 M H<sub>2</sub>SO<sub>4</sub> (electrolyte) and their electrochemical oxidation in the electrolyte. The electrochemical cell was upsized by stacking eight single-compartment cells, permitting the circulation of the absorbent in series. The results showed the successful removal of BTX from a synthetic gas stream, which increased at high current densities and low gas flow rates. Average removals over 60 % were achieved in the electro-absorption with 50 mA cm<sup>−2</sup>. Analysis of the contaminants in the electrolyte confirmed the absorption of BTXs and their electrochemical oxidation by mineralisation, which was enhanced at larger gas flows and current densities. Nevertheless, a comparison of equivalent scaled and baseline systems indicated an inferior current efficiency on the larger scale due to mass transfer inefficiencies, which are affected by circulating the absorbent in series. These findings suggest that the replication of single electrochemical cells (parallel) can optimise the performance of the electro-absorption degradation of BTX at larger scales.</div></div>","PeriodicalId":355,"journal":{"name":"Journal of Electroanalytical Chemistry","volume":"981 ","pages":"Article 118998"},"PeriodicalIF":4.1000,"publicationDate":"2025-02-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Electroanalytical Chemistry","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1572665725000712","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
引用次数: 0
Abstract
Electrochemical technologies have proven highly efficient in remediating polluted gas with benzene, toluene, and xylene (BTX). However, their scalability has yet to be explored to determine the best configurations to maintain optimal removals and energetic efficiencies. Here, we report a straightforward scale-up of an electro-absorption process that combines the absorption of BTX in 0.05 M H2SO4 (electrolyte) and their electrochemical oxidation in the electrolyte. The electrochemical cell was upsized by stacking eight single-compartment cells, permitting the circulation of the absorbent in series. The results showed the successful removal of BTX from a synthetic gas stream, which increased at high current densities and low gas flow rates. Average removals over 60 % were achieved in the electro-absorption with 50 mA cm−2. Analysis of the contaminants in the electrolyte confirmed the absorption of BTXs and their electrochemical oxidation by mineralisation, which was enhanced at larger gas flows and current densities. Nevertheless, a comparison of equivalent scaled and baseline systems indicated an inferior current efficiency on the larger scale due to mass transfer inefficiencies, which are affected by circulating the absorbent in series. These findings suggest that the replication of single electrochemical cells (parallel) can optimise the performance of the electro-absorption degradation of BTX at larger scales.
期刊介绍:
The Journal of Electroanalytical Chemistry is the foremost international journal devoted to the interdisciplinary subject of electrochemistry in all its aspects, theoretical as well as applied.
Electrochemistry is a wide ranging area that is in a state of continuous evolution. Rather than compiling a long list of topics covered by the Journal, the editors would like to draw particular attention to the key issues of novelty, topicality and quality. Papers should present new and interesting electrochemical science in a way that is accessible to the reader. The presentation and discussion should be at a level that is consistent with the international status of the Journal. Reports describing the application of well-established techniques to problems that are essentially technical will not be accepted. Similarly, papers that report observations but fail to provide adequate interpretation will be rejected by the Editors. Papers dealing with technical electrochemistry should be submitted to other specialist journals unless the authors can show that their work provides substantially new insights into electrochemical processes.