生物质吸附剂的大气吸水动力学:初步研究

IF 1.7 4区 化学 Q4 CHEMISTRY, PHYSICAL Reaction Kinetics, Mechanisms and Catalysis Pub Date : 2024-08-09 DOI:10.1007/s11144-024-02694-y
G. Raveesh, R. Goyal, S. K. Tyagi
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引用次数: 0

摘要

本研究旨在研究在半干旱和半湿润的实时条件下,从废弃甘蔗生物质中提取的 CaCl2 盐浸渍吸附剂对大气水的吸附动力学。根据吸水和吸附动力学,初步筛选了将废弃甘蔗渣制备的高孔活性炭浸渍在不同浓度 CaCl2 盐中制备的样品。随后,对筛选出的吸附剂进行进一步表征,以评估其质地特性、表面形态、热稳定性、官能团和密度。在 30% 到 50% 的低相对湿度条件下,该吸水剂的吸水率在 0.71 到 0.95 克/克之间,吸附和解吸动力学速度很快。该吸附剂还在 10 个吸附-解吸循环中表现出操作稳定性。还利用线性驱动力(LDF)模型对实验吸水数据进行了拟合,以确定吸附速率常数,结果与模型非常吻合。此外,在 60 °C 时,解吸率超过 80%,这表明太阳能辅助操作是可行的。这项研究凸显了从废弃生物质中提取的吸附剂在可持续 AWH 应用中的潜力。
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Atmospheric water sorption kinetics of a biomass-derived sorbent: a preliminary study

This study aims to investigate the atmospheric water sorption kinetics of a CaCl2 salt-impregnated sorbent derived from waste sugarcane biomass under real-time semi-arid to semi-humid conditions. The samples prepared by impregnating highly porous activated carbon prepared from waste sugarcane bagasse in different salt concentrations of CaCl2 was initially screened based on its water uptake and sorption kinetics. Subsequently, the screened sorbent underwent further characterization to assess its textural properties, surface morphology, thermal stability, functional groups, and density. Under low relative humidity (RH) conditions ranging from 30 to 50%, the sorbent exhibited commendable water uptake ranging between 0.71 and 0.95 g/g, coupled with rapid adsorption and desorption kinetics. The sorbent also demonstrated operational stability over 10 adsorption–desorption cycles. The experimental water uptake data was also fitted using the Linear Driving Force (LDF) model to determine the sorption rate constant and resulted in a very good agreement with the model. Furthermore, at 60 °C, more than 80% desorption was attained, indicating the feasibility of solar-assisted operation. This study highlights the potential of sorbents derived from waste biomass for sustainable AWH applications.

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来源期刊
CiteScore
3.30
自引率
5.60%
发文量
201
审稿时长
2.8 months
期刊介绍: Reaction Kinetics, Mechanisms and Catalysis is a medium for original contributions in the following fields: -kinetics of homogeneous reactions in gas, liquid and solid phase; -Homogeneous catalysis; -Heterogeneous catalysis; -Adsorption in heterogeneous catalysis; -Transport processes related to reaction kinetics and catalysis; -Preparation and study of catalysts; -Reactors and apparatus. Reaction Kinetics, Mechanisms and Catalysis was formerly published under the title Reaction Kinetics and Catalysis Letters.
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