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Sour Gas Adsorption on Silica Gels

[Image: see text] One of the essential factors for water adsorption on silica gels is the concentration of silanol groups on the silica surface. However, no systematic investigation on the adsorption of sour gas components, methane (CH(4)), carbon dioxide (CO(2)), and hydrogen sulfide (H(2)S) on sil...

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Autores principales: Jacobs, John H., McKelvie, Kaylan H., Nanji, Safeer, Marriott, Robert A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10077463/
https://www.ncbi.nlm.nih.gov/pubmed/37033864
http://dx.doi.org/10.1021/acsomega.3c01366
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author Jacobs, John H.
McKelvie, Kaylan H.
Nanji, Safeer
Marriott, Robert A.
author_facet Jacobs, John H.
McKelvie, Kaylan H.
Nanji, Safeer
Marriott, Robert A.
author_sort Jacobs, John H.
collection PubMed
description [Image: see text] One of the essential factors for water adsorption on silica gels is the concentration of silanol groups on the silica surface. However, no systematic investigation on the adsorption of sour gas components, methane (CH(4)), carbon dioxide (CO(2)), and hydrogen sulfide (H(2)S) on silica gels with different textural properties and surface silanol concentrations, has been conducted. Three silica gels of 22, 30, and 60 Å pore sizes, with silanol concentrations of α(total) = 2.516, 2.340, and 2.152 OH nm(–2), respectively, were studied in this work. The adsorption data for CH(4), CO(2), H(2)S, and H(2)O at T = 0, 25, and 50 °C on the 22 and 30 Å pore size silica gels were presented, and a comparison of the data for the 60 Å pore size silica gel on the same adsorbates was conducted. All three silica gels showed an adsorption affinity in the order of H(2)O > H(2)S > CO(2) > CH(4). The isosteric heats of adsorption of H(2)O and H(2)S had a greater dependence on the silanol concentration than CO(2) and CH(4). At p < 10 bar, there was no difference in the adsorption per m(2) of CH(4) between the silica gels (n(ads) = 1.7 mmol m(–2), for all silicas at p = 10 bar), while higher pressures resulted in greater adsorption capacity in the larger pore volume silica gels (at p = 20 bar: n(ads) = 3.0, 3.3, and 3.4 mmol m(–2) for the 22, 30, and 60 Å pore size silicas, respectively). H(2)S adsorption at low pressures (p < 4 bar) was larger on the samples with larger silanol concentrations (at p = 3 bar: n(ads) = 6.1, 4.7, and 4.5 mmol m(–2) for the 22, 30, and 60 Å pore size silicas, respectively), but above p = 4 bar, the 60 Å pore size silica had a greater adsorption capacity than the 30 Å pore size (at p = 5 bar: n(ads) = 8.0, 6.0, and 6.2 mmol m(–2) for the 22, 30, and 60 Å pore size silicas, respectively).
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spelling pubmed-100774632023-04-07 Sour Gas Adsorption on Silica Gels Jacobs, John H. McKelvie, Kaylan H. Nanji, Safeer Marriott, Robert A. ACS Omega [Image: see text] One of the essential factors for water adsorption on silica gels is the concentration of silanol groups on the silica surface. However, no systematic investigation on the adsorption of sour gas components, methane (CH(4)), carbon dioxide (CO(2)), and hydrogen sulfide (H(2)S) on silica gels with different textural properties and surface silanol concentrations, has been conducted. Three silica gels of 22, 30, and 60 Å pore sizes, with silanol concentrations of α(total) = 2.516, 2.340, and 2.152 OH nm(–2), respectively, were studied in this work. The adsorption data for CH(4), CO(2), H(2)S, and H(2)O at T = 0, 25, and 50 °C on the 22 and 30 Å pore size silica gels were presented, and a comparison of the data for the 60 Å pore size silica gel on the same adsorbates was conducted. All three silica gels showed an adsorption affinity in the order of H(2)O > H(2)S > CO(2) > CH(4). The isosteric heats of adsorption of H(2)O and H(2)S had a greater dependence on the silanol concentration than CO(2) and CH(4). At p < 10 bar, there was no difference in the adsorption per m(2) of CH(4) between the silica gels (n(ads) = 1.7 mmol m(–2), for all silicas at p = 10 bar), while higher pressures resulted in greater adsorption capacity in the larger pore volume silica gels (at p = 20 bar: n(ads) = 3.0, 3.3, and 3.4 mmol m(–2) for the 22, 30, and 60 Å pore size silicas, respectively). H(2)S adsorption at low pressures (p < 4 bar) was larger on the samples with larger silanol concentrations (at p = 3 bar: n(ads) = 6.1, 4.7, and 4.5 mmol m(–2) for the 22, 30, and 60 Å pore size silicas, respectively), but above p = 4 bar, the 60 Å pore size silica had a greater adsorption capacity than the 30 Å pore size (at p = 5 bar: n(ads) = 8.0, 6.0, and 6.2 mmol m(–2) for the 22, 30, and 60 Å pore size silicas, respectively). American Chemical Society 2023-03-22 /pmc/articles/PMC10077463/ /pubmed/37033864 http://dx.doi.org/10.1021/acsomega.3c01366 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Jacobs, John H.
McKelvie, Kaylan H.
Nanji, Safeer
Marriott, Robert A.
Sour Gas Adsorption on Silica Gels
title Sour Gas Adsorption on Silica Gels
title_full Sour Gas Adsorption on Silica Gels
title_fullStr Sour Gas Adsorption on Silica Gels
title_full_unstemmed Sour Gas Adsorption on Silica Gels
title_short Sour Gas Adsorption on Silica Gels
title_sort sour gas adsorption on silica gels
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10077463/
https://www.ncbi.nlm.nih.gov/pubmed/37033864
http://dx.doi.org/10.1021/acsomega.3c01366
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