Minghui Hu , Zhipeng Qie , Zhongbao Liu , Xuanpeng Lu , Shiyang Bai , Li Lv , Zepeng Wang , Huaizhong Xiang , Xiaoxia Ou , Yuanye Zhuang
{"title":"Sequential carboxylic acid and ammonium hydroxide treatments for zeolites: Enhancing CO2 adsorption under humid conditions","authors":"Minghui Hu , Zhipeng Qie , Zhongbao Liu , Xuanpeng Lu , Shiyang Bai , Li Lv , Zepeng Wang , Huaizhong Xiang , Xiaoxia Ou , Yuanye Zhuang","doi":"10.1016/j.micromeso.2024.113465","DOIUrl":null,"url":null,"abstract":"<div><div>High-performance carbon dioxide (CO<sub>2</sub>) capture in environments with high humidity remains a significant challenge. In this study, we proposed a sequential post-treatment method using carboxylic acids (oxalic acid, OA, and ethylenediaminetetraacetic acid, EDTA) followed by ammonium hydroxide (NH<sub>4</sub>OH) treatment to enhance the CO<sub>2</sub>/H<sub>2</sub>O adsorption selectivity of zeolite adsorbents. This method was found effective for Y, Beta, and MOR zeolites, in which MOR zeolites with sequential OA and NH<sub>4</sub>OH (OA-NH<sub>4</sub>OH) treatment demonstrated the optimal CO<sub>2</sub>/H<sub>2</sub>O selectivity and the longest CO<sub>2</sub> breakthrough time in dynamic adsorption at 75 % relative humidity (RH). The outstanding performance can be attributed to its well-preserved porosity and improved surface silicon-to-aluminum ratio. Based on advanced characterizations such as CO<sub>2</sub> physisorption and solid state <sup>27</sup>Al NMR, the mechanism for OA-NH<sub>4</sub> treatment was proposed as follows: first, OA treatment increased the micropore volume by restoring partially coordinated Al (IV-2) species, subsequently, NH<sub>4</sub>OH treatment removed Al (VI) (i.e., extra framework Al species) from the MOR zeolites. The sequential OA-NH<sub>4</sub>OH treatment collectively boosted the zeolite's affinity for CO<sub>2</sub>. Additionally, the modified zeolite adsorbent exhibited excellent recyclability, with a CO<sub>2</sub> adsorption capacity loss of less than 1 wt% over five cycles. This study offers new insights into developing “water-resistant” zeolite adsorbents through simple post-treatment approaches.</div></div>","PeriodicalId":392,"journal":{"name":"Microporous and Mesoporous Materials","volume":"384 ","pages":"Article 113465"},"PeriodicalIF":4.8000,"publicationDate":"2024-12-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Microporous and Mesoporous Materials","FirstCategoryId":"88","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1387181124004876","RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, APPLIED","Score":null,"Total":0}
引用次数: 0
Abstract
High-performance carbon dioxide (CO2) capture in environments with high humidity remains a significant challenge. In this study, we proposed a sequential post-treatment method using carboxylic acids (oxalic acid, OA, and ethylenediaminetetraacetic acid, EDTA) followed by ammonium hydroxide (NH4OH) treatment to enhance the CO2/H2O adsorption selectivity of zeolite adsorbents. This method was found effective for Y, Beta, and MOR zeolites, in which MOR zeolites with sequential OA and NH4OH (OA-NH4OH) treatment demonstrated the optimal CO2/H2O selectivity and the longest CO2 breakthrough time in dynamic adsorption at 75 % relative humidity (RH). The outstanding performance can be attributed to its well-preserved porosity and improved surface silicon-to-aluminum ratio. Based on advanced characterizations such as CO2 physisorption and solid state 27Al NMR, the mechanism for OA-NH4 treatment was proposed as follows: first, OA treatment increased the micropore volume by restoring partially coordinated Al (IV-2) species, subsequently, NH4OH treatment removed Al (VI) (i.e., extra framework Al species) from the MOR zeolites. The sequential OA-NH4OH treatment collectively boosted the zeolite's affinity for CO2. Additionally, the modified zeolite adsorbent exhibited excellent recyclability, with a CO2 adsorption capacity loss of less than 1 wt% over five cycles. This study offers new insights into developing “water-resistant” zeolite adsorbents through simple post-treatment approaches.
期刊介绍:
Microporous and Mesoporous Materials covers novel and significant aspects of porous solids classified as either microporous (pore size up to 2 nm) or mesoporous (pore size 2 to 50 nm). The porosity should have a specific impact on the material properties or application. Typical examples are zeolites and zeolite-like materials, pillared materials, clathrasils and clathrates, carbon molecular sieves, ordered mesoporous materials, organic/inorganic porous hybrid materials, or porous metal oxides. Both natural and synthetic porous materials are within the scope of the journal.
Topics which are particularly of interest include:
All aspects of natural microporous and mesoporous solids
The synthesis of crystalline or amorphous porous materials
The physico-chemical characterization of microporous and mesoporous solids, especially spectroscopic and microscopic
The modification of microporous and mesoporous solids, for example by ion exchange or solid-state reactions
All topics related to diffusion of mobile species in the pores of microporous and mesoporous materials
Adsorption (and other separation techniques) using microporous or mesoporous adsorbents
Catalysis by microporous and mesoporous materials
Host/guest interactions
Theoretical chemistry and modelling of host/guest interactions
All topics related to the application of microporous and mesoporous materials in industrial catalysis, separation technology, environmental protection, electrochemistry, membranes, sensors, optical devices, etc.