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Core Shell Nanostructure: Impregnated Activated Carbon as Adsorbent for Hydrogen Sulfide Adsorption

This study focuses on the synthesis, characterization, and evaluation of the performance of core shell nanostructure adsorbent for hydrogen sulfide (H(2)S) capture. Commercial coconut shell activated carbon (CAC) and commercial mixed gas of 5000 ppm H(2)S balanced N(2) were used. With different prep...

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Autores principales: Zulkefli, Nurul Noramelya, Seladorai, Rajeevelosana, Masdar, Mohd Shahbudin, Mohd Sofian, Nabilah, Wan Isahak, Wan Nor Roslam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8838705/
https://www.ncbi.nlm.nih.gov/pubmed/35164410
http://dx.doi.org/10.3390/molecules27031145
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author Zulkefli, Nurul Noramelya
Seladorai, Rajeevelosana
Masdar, Mohd Shahbudin
Mohd Sofian, Nabilah
Wan Isahak, Wan Nor Roslam
author_facet Zulkefli, Nurul Noramelya
Seladorai, Rajeevelosana
Masdar, Mohd Shahbudin
Mohd Sofian, Nabilah
Wan Isahak, Wan Nor Roslam
author_sort Zulkefli, Nurul Noramelya
collection PubMed
description This study focuses on the synthesis, characterization, and evaluation of the performance of core shell nanostructure adsorbent for hydrogen sulfide (H(2)S) capture. Commercial coconut shell activated carbon (CAC) and commercial mixed gas of 5000 ppm H(2)S balanced N(2) were used. With different preparation techniques, the CAC was modified by core shell impregnation with zinc oxide (ZnO), titanium oxide (TiO(2)), potassium hydroxide (KOH), and zinc acetate (ZnAC(2)). The core structure was prepared with CAC impregnated by single chemical and double chemical labelled with ZnAC(2)-CAC (single chemical), ZnAC(2)/KOH-CAC, ZnAC(2)/ZnO-CAC, and ZnAC(2)/TiO(2)-CAC. Then, the prepared core was layered either with KOH, TiO(2), NH(3), or TEOS for the shell. The synthesized adsorbents were characterized in physical and chemical characterization through scanning electron microscopy (SEM), thermal gravimetric analysis (TGA), and Brunauer-Emmett-Teller (BET) analyzers. Operation of the adsorber column takes place at ambient temperature, with absolute pressure at 1.5 bar. The H(2)S gas was fed into the column at 5.5 L/min and the loaded adsorbents were 150 g. The performance of synthesized adsorbent was analyzed through the adsorbent’s capability in capturing H(2)S gas. Based on the results, ZnAc(2)/ZnO/CAC_WOS shows a better adsorption capacity with 1.17 mg H(2)S/g and a 53% increment compared to raw CAC. However, the degradation of the adsorbents was higher compared to ZnAc(2)/ZnO/CAC_OS and to ZnAc(2)/ZnO/CAC_WS ZnAc(2)/ZnO/CAC_OS. The presence of silica as a shell has potentially increased the adsorbent’s stability in several cycles of adsorption-desorption.
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spelling pubmed-88387052022-02-13 Core Shell Nanostructure: Impregnated Activated Carbon as Adsorbent for Hydrogen Sulfide Adsorption Zulkefli, Nurul Noramelya Seladorai, Rajeevelosana Masdar, Mohd Shahbudin Mohd Sofian, Nabilah Wan Isahak, Wan Nor Roslam Molecules Article This study focuses on the synthesis, characterization, and evaluation of the performance of core shell nanostructure adsorbent for hydrogen sulfide (H(2)S) capture. Commercial coconut shell activated carbon (CAC) and commercial mixed gas of 5000 ppm H(2)S balanced N(2) were used. With different preparation techniques, the CAC was modified by core shell impregnation with zinc oxide (ZnO), titanium oxide (TiO(2)), potassium hydroxide (KOH), and zinc acetate (ZnAC(2)). The core structure was prepared with CAC impregnated by single chemical and double chemical labelled with ZnAC(2)-CAC (single chemical), ZnAC(2)/KOH-CAC, ZnAC(2)/ZnO-CAC, and ZnAC(2)/TiO(2)-CAC. Then, the prepared core was layered either with KOH, TiO(2), NH(3), or TEOS for the shell. The synthesized adsorbents were characterized in physical and chemical characterization through scanning electron microscopy (SEM), thermal gravimetric analysis (TGA), and Brunauer-Emmett-Teller (BET) analyzers. Operation of the adsorber column takes place at ambient temperature, with absolute pressure at 1.5 bar. The H(2)S gas was fed into the column at 5.5 L/min and the loaded adsorbents were 150 g. The performance of synthesized adsorbent was analyzed through the adsorbent’s capability in capturing H(2)S gas. Based on the results, ZnAc(2)/ZnO/CAC_WOS shows a better adsorption capacity with 1.17 mg H(2)S/g and a 53% increment compared to raw CAC. However, the degradation of the adsorbents was higher compared to ZnAc(2)/ZnO/CAC_OS and to ZnAc(2)/ZnO/CAC_WS ZnAc(2)/ZnO/CAC_OS. The presence of silica as a shell has potentially increased the adsorbent’s stability in several cycles of adsorption-desorption. MDPI 2022-02-08 /pmc/articles/PMC8838705/ /pubmed/35164410 http://dx.doi.org/10.3390/molecules27031145 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Zulkefli, Nurul Noramelya
Seladorai, Rajeevelosana
Masdar, Mohd Shahbudin
Mohd Sofian, Nabilah
Wan Isahak, Wan Nor Roslam
Core Shell Nanostructure: Impregnated Activated Carbon as Adsorbent for Hydrogen Sulfide Adsorption
title Core Shell Nanostructure: Impregnated Activated Carbon as Adsorbent for Hydrogen Sulfide Adsorption
title_full Core Shell Nanostructure: Impregnated Activated Carbon as Adsorbent for Hydrogen Sulfide Adsorption
title_fullStr Core Shell Nanostructure: Impregnated Activated Carbon as Adsorbent for Hydrogen Sulfide Adsorption
title_full_unstemmed Core Shell Nanostructure: Impregnated Activated Carbon as Adsorbent for Hydrogen Sulfide Adsorption
title_short Core Shell Nanostructure: Impregnated Activated Carbon as Adsorbent for Hydrogen Sulfide Adsorption
title_sort core shell nanostructure: impregnated activated carbon as adsorbent for hydrogen sulfide adsorption
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8838705/
https://www.ncbi.nlm.nih.gov/pubmed/35164410
http://dx.doi.org/10.3390/molecules27031145
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