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Alkyl chain length of quaternized SBA-15 and solution conditions determine hydrophobic and electrostatic interactions for carbamazepine adsorption

Santa Barbara Amorphous-15 (SBA) is a stable and mesoporous silica material. Quaternized SBA-15 with alkyl chains (Q(SBA)) exhibits electrostatic attraction for anionic molecules via the N(+) moiety of the ammonium group, whereas its alkyl chain length determines its hydrophobic interactions. In thi...

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Autores principales: Kang, Jin-Kyu, Lee, Hyebin, Kim, Song-Bae, Bae, Hyokwan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10063578/
https://www.ncbi.nlm.nih.gov/pubmed/36997526
http://dx.doi.org/10.1038/s41598-023-32108-3
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author Kang, Jin-Kyu
Lee, Hyebin
Kim, Song-Bae
Bae, Hyokwan
author_facet Kang, Jin-Kyu
Lee, Hyebin
Kim, Song-Bae
Bae, Hyokwan
author_sort Kang, Jin-Kyu
collection PubMed
description Santa Barbara Amorphous-15 (SBA) is a stable and mesoporous silica material. Quaternized SBA-15 with alkyl chains (Q(SBA)) exhibits electrostatic attraction for anionic molecules via the N(+) moiety of the ammonium group, whereas its alkyl chain length determines its hydrophobic interactions. In this study, Q(SBA) with different alkyl chain lengths were synthesized using the trimethyl, dimethyloctyl, and dimethyoctadecyl groups (C1Q(SBA), C8Q(SBA), and C18Q(SBA), respectively). Carbamazepine (CBZ) is a widely prescribed pharmaceutical compound, but is difficult to remove using conventional water treatments. The CBZ adsorption characteristics of Q(SBA) were examined to determine its adsorption mechanism by changing the alkyl chain length and solution conditions (pH and ionic strength). A longer alkyl chain resulted in slower adsorption (up to 120 min), while the amount of CBZ adsorbed was higher for longer alkyl chains per unit mass of Q(SBA) at equilibrium. The maximum adsorption capacities of C1Q(SBA), C8Q(SBA), and C18Q(SBA), were 3.14, 6.56, and 24.5 mg/g, respectively, as obtained using the Langmuir model. For the tested initial CBZ concentrations (2–100 mg/L), the adsorption capacity increased with increasing alkyl chain length. Because CBZ does not dissociate readily (pK(a) = 13.9), stable hydrophobic adsorption was observed despite the changes in pH (0.41–0.92, 1.70–2.24, and 7.56–9.10 mg/g for C1Q(SBA), C8Q(SBA), and C18Q(SBA), respectively); the exception was pH 2. Increasing the ionic strength from 0.1 to 100 mM enhanced the adsorption capacity of C18Q(SBA) from 9.27 ± 0.42 to 14.94 ± 0.17 mg/g because the hydrophobic interactions were increased while the electrostatic attraction of the N(+) was reduced. Thus, the ionic strength was a stronger control factor determining hydrophobic adsorption of CBZ than the solution pH. Based on the changes in hydrophobicity, which depends on the alkyl chain length, it was possible to enhance CBZ adsorption and investigate the adsorption mechanism in detail. Thus, this study aids the development of adsorbents suitable for pharmaceuticals with controlling molecular structure of QSBA and solution conditions.
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spelling pubmed-100635782023-04-01 Alkyl chain length of quaternized SBA-15 and solution conditions determine hydrophobic and electrostatic interactions for carbamazepine adsorption Kang, Jin-Kyu Lee, Hyebin Kim, Song-Bae Bae, Hyokwan Sci Rep Article Santa Barbara Amorphous-15 (SBA) is a stable and mesoporous silica material. Quaternized SBA-15 with alkyl chains (Q(SBA)) exhibits electrostatic attraction for anionic molecules via the N(+) moiety of the ammonium group, whereas its alkyl chain length determines its hydrophobic interactions. In this study, Q(SBA) with different alkyl chain lengths were synthesized using the trimethyl, dimethyloctyl, and dimethyoctadecyl groups (C1Q(SBA), C8Q(SBA), and C18Q(SBA), respectively). Carbamazepine (CBZ) is a widely prescribed pharmaceutical compound, but is difficult to remove using conventional water treatments. The CBZ adsorption characteristics of Q(SBA) were examined to determine its adsorption mechanism by changing the alkyl chain length and solution conditions (pH and ionic strength). A longer alkyl chain resulted in slower adsorption (up to 120 min), while the amount of CBZ adsorbed was higher for longer alkyl chains per unit mass of Q(SBA) at equilibrium. The maximum adsorption capacities of C1Q(SBA), C8Q(SBA), and C18Q(SBA), were 3.14, 6.56, and 24.5 mg/g, respectively, as obtained using the Langmuir model. For the tested initial CBZ concentrations (2–100 mg/L), the adsorption capacity increased with increasing alkyl chain length. Because CBZ does not dissociate readily (pK(a) = 13.9), stable hydrophobic adsorption was observed despite the changes in pH (0.41–0.92, 1.70–2.24, and 7.56–9.10 mg/g for C1Q(SBA), C8Q(SBA), and C18Q(SBA), respectively); the exception was pH 2. Increasing the ionic strength from 0.1 to 100 mM enhanced the adsorption capacity of C18Q(SBA) from 9.27 ± 0.42 to 14.94 ± 0.17 mg/g because the hydrophobic interactions were increased while the electrostatic attraction of the N(+) was reduced. Thus, the ionic strength was a stronger control factor determining hydrophobic adsorption of CBZ than the solution pH. Based on the changes in hydrophobicity, which depends on the alkyl chain length, it was possible to enhance CBZ adsorption and investigate the adsorption mechanism in detail. Thus, this study aids the development of adsorbents suitable for pharmaceuticals with controlling molecular structure of QSBA and solution conditions. Nature Publishing Group UK 2023-03-30 /pmc/articles/PMC10063578/ /pubmed/36997526 http://dx.doi.org/10.1038/s41598-023-32108-3 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Kang, Jin-Kyu
Lee, Hyebin
Kim, Song-Bae
Bae, Hyokwan
Alkyl chain length of quaternized SBA-15 and solution conditions determine hydrophobic and electrostatic interactions for carbamazepine adsorption
title Alkyl chain length of quaternized SBA-15 and solution conditions determine hydrophobic and electrostatic interactions for carbamazepine adsorption
title_full Alkyl chain length of quaternized SBA-15 and solution conditions determine hydrophobic and electrostatic interactions for carbamazepine adsorption
title_fullStr Alkyl chain length of quaternized SBA-15 and solution conditions determine hydrophobic and electrostatic interactions for carbamazepine adsorption
title_full_unstemmed Alkyl chain length of quaternized SBA-15 and solution conditions determine hydrophobic and electrostatic interactions for carbamazepine adsorption
title_short Alkyl chain length of quaternized SBA-15 and solution conditions determine hydrophobic and electrostatic interactions for carbamazepine adsorption
title_sort alkyl chain length of quaternized sba-15 and solution conditions determine hydrophobic and electrostatic interactions for carbamazepine adsorption
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10063578/
https://www.ncbi.nlm.nih.gov/pubmed/36997526
http://dx.doi.org/10.1038/s41598-023-32108-3
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