LAPSE:2023.1556
Published Article

LAPSE:2023.1556
Activated Carbon Modified by Ester Hydrolysis of Ethyl Acetate for Water Vapor Adsorption Enhancement
February 21, 2023
Abstract
To improve water vapor adsorption, this study employed oxalic acid−ethyl acetate acidic hydrolysis to modify honeycomb activated carbon and introduce hydrophilic functional groups. Scanning electron microscopy (SEM), Boehm titration, Fourier transform infrared spectroscopy (FT-IR), and an automatic surface area analyzer (BET) were used to characterize the microscopic morphology, surface functional groups, specific surface area, and pore size changes. The results showed that, when the concentration of oxalic acid is 0.0006 mol/cm3, the specific surface area is 179.06 m2/g. After hydrolysis with ethyl acetate, the original functional groups became more abundant, while the number of total acidic functional groups on the surface grew from 0.497 mmol/g to 1.437 mmol/g. The static water vapor adsorption experiments were conducted on modified activated carbon under constant temperature and humidity conditions. Compared with unmodified activated carbon, the activated carbon modified with 0.0006 mol/cm3 oxalic acid increased the adsorption capacity of water vapor by 15.7%. The adsorption capacity of activated carbon after being combined with 0.0006 mol/cm3 oxalic acid and ester hydrolysis modification increased by 37.1%. At the same temperature, the adsorption capacity increased with a higher relative humidity. At the same relative humidity, the adsorption capacity decreased as the temperature rose. Therefore, this modification method may provide clues for the application of enhancing the hygroscopic ability of activated carbon.
To improve water vapor adsorption, this study employed oxalic acid−ethyl acetate acidic hydrolysis to modify honeycomb activated carbon and introduce hydrophilic functional groups. Scanning electron microscopy (SEM), Boehm titration, Fourier transform infrared spectroscopy (FT-IR), and an automatic surface area analyzer (BET) were used to characterize the microscopic morphology, surface functional groups, specific surface area, and pore size changes. The results showed that, when the concentration of oxalic acid is 0.0006 mol/cm3, the specific surface area is 179.06 m2/g. After hydrolysis with ethyl acetate, the original functional groups became more abundant, while the number of total acidic functional groups on the surface grew from 0.497 mmol/g to 1.437 mmol/g. The static water vapor adsorption experiments were conducted on modified activated carbon under constant temperature and humidity conditions. Compared with unmodified activated carbon, the activated carbon modified with 0.0006 mol/cm3 oxalic acid increased the adsorption capacity of water vapor by 15.7%. The adsorption capacity of activated carbon after being combined with 0.0006 mol/cm3 oxalic acid and ester hydrolysis modification increased by 37.1%. At the same temperature, the adsorption capacity increased with a higher relative humidity. At the same relative humidity, the adsorption capacity decreased as the temperature rose. Therefore, this modification method may provide clues for the application of enhancing the hygroscopic ability of activated carbon.
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Keywords
activated carbon, ester hydrolysis, modification, water vapor adsorption
Subject
Suggested Citation
Xu J, Zhang H, Ji X, Lan Q, Fan Q. Activated Carbon Modified by Ester Hydrolysis of Ethyl Acetate for Water Vapor Adsorption Enhancement. (2023). LAPSE:2023.1556
Author Affiliations
Xu J: Education Ministry Key Laboratory of Renewable Energy Advanced Materials and Manufacturing Technology, School of Energy and Environmental Science, Yunnan Normal University, Kunming 650500, China
Zhang H: Education Ministry Key Laboratory of Renewable Energy Advanced Materials and Manufacturing Technology, School of Energy and Environmental Science, Yunnan Normal University, Kunming 650500, China
Ji X: Education Ministry Key Laboratory of Renewable Energy Advanced Materials and Manufacturing Technology, School of Energy and Environmental Science, Yunnan Normal University, Kunming 650500, China; Yunnan Key Laboratory of Optoelectronic Information Technol
Lan Q: Education Ministry Key Laboratory of Renewable Energy Advanced Materials and Manufacturing Technology, School of Energy and Environmental Science, Yunnan Normal University, Kunming 650500, China
Fan Q: Education Ministry Key Laboratory of Renewable Energy Advanced Materials and Manufacturing Technology, School of Energy and Environmental Science, Yunnan Normal University, Kunming 650500, China
Zhang H: Education Ministry Key Laboratory of Renewable Energy Advanced Materials and Manufacturing Technology, School of Energy and Environmental Science, Yunnan Normal University, Kunming 650500, China
Ji X: Education Ministry Key Laboratory of Renewable Energy Advanced Materials and Manufacturing Technology, School of Energy and Environmental Science, Yunnan Normal University, Kunming 650500, China; Yunnan Key Laboratory of Optoelectronic Information Technol
Lan Q: Education Ministry Key Laboratory of Renewable Energy Advanced Materials and Manufacturing Technology, School of Energy and Environmental Science, Yunnan Normal University, Kunming 650500, China
Fan Q: Education Ministry Key Laboratory of Renewable Energy Advanced Materials and Manufacturing Technology, School of Energy and Environmental Science, Yunnan Normal University, Kunming 650500, China
Journal Name
Processes
Volume
10
Issue
8
First Page
1527
Year
2022
Publication Date
2022-08-03
ISSN
2227-9717
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Original Submission
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PII: pr10081527, Publication Type: Journal Article
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LAPSE:2023.1556
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https://doi.org/10.3390/pr10081527
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