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Catalytic dechlorination of 1,2-DCA in nano Cu(0)-borohydride system: effects of Cu(0)/Cu(n+) ratio, surface poisoning, and regeneration of Cu(0) sites
Aqueous-phase catalyzed reduction of organic contaminants via zerovalent copper nanoparticles (nCu(0)), coupled with borohydride (hydrogen donor), has shown promising results. So far, the research on nCu(0) as a remedial treatment has focused mainly on contaminant removal efficiencies and degradatio...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10363550/ https://www.ncbi.nlm.nih.gov/pubmed/37482593 http://dx.doi.org/10.1038/s41598-023-38678-6 |
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author | Boparai, Hardiljeet Kaur El-Sharnouby, Omneya O’Carroll, Denis M. |
author_facet | Boparai, Hardiljeet Kaur El-Sharnouby, Omneya O’Carroll, Denis M. |
author_sort | Boparai, Hardiljeet Kaur |
collection | PubMed |
description | Aqueous-phase catalyzed reduction of organic contaminants via zerovalent copper nanoparticles (nCu(0)), coupled with borohydride (hydrogen donor), has shown promising results. So far, the research on nCu(0) as a remedial treatment has focused mainly on contaminant removal efficiencies and degradation mechanisms. Our study has examined the effects of Cu(0)/Cu(n+) ratio, surface poisoning (presence of chloride, sulfides, humic acid (HA)), and regeneration of Cu(0) sites on catalytic dechlorination of aqueous-phase 1,2-dichloroethane (1,2-DCA) via nCu(0)-borohydride. Scanning electron microscopy confirmed the nano size and quasi-spherical shape of nCu(0) particles. X-ray diffraction confirmed the presence of Cu(0) and Cu(2)O and x-ray photoelectron spectroscopy also provided the Cu(0)/Cu(n+) ratios. Reactivity experiments showed that nCu(0) was incapable of utilizing H(2) from borohydride left over during nCu(0) synthesis and, hence, additional borohydride was essential for 1,2-DCA dechlorination. Washing the nCu(0) particles improved their Cu(0)/Cu(n+) ratio (1.27) and 92% 1,2-DCA was removed in 7 h with k(obs) = 0.345 h(−1) as compared to only 44% by unwashed nCu(0) (0.158 h(−1)) with Cu(0)/Cu(n+) ratio of 0.59, in the presence of borohydride. The presence of chloride (1000–2000 mg L(−1)), sulfides (0.4–4 mg L(−1)), and HA (10–30 mg L(−1)) suppressed 1,2-DCA dechlorination; which was improved by additional borohydride probably via regeneration of Cu(0) sites. Coating the particles decreased their catalytic dechlorination efficiency. 85–90% of the removed 1,2-DCA was recovered as chloride. Chloroethane and ethane were main dechlorination products indicating hydrogenolysis as the major pathway. Our results imply that synthesis parameters and groundwater solutes control nCu(0) catalytic activity by altering its physico-chemical properties. Thus, these factors should be considered to develop an efficient remedial design for practical applications of nCu(0)-borohydride. |
format | Online Article Text |
id | pubmed-10363550 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-103635502023-07-25 Catalytic dechlorination of 1,2-DCA in nano Cu(0)-borohydride system: effects of Cu(0)/Cu(n+) ratio, surface poisoning, and regeneration of Cu(0) sites Boparai, Hardiljeet Kaur El-Sharnouby, Omneya O’Carroll, Denis M. Sci Rep Article Aqueous-phase catalyzed reduction of organic contaminants via zerovalent copper nanoparticles (nCu(0)), coupled with borohydride (hydrogen donor), has shown promising results. So far, the research on nCu(0) as a remedial treatment has focused mainly on contaminant removal efficiencies and degradation mechanisms. Our study has examined the effects of Cu(0)/Cu(n+) ratio, surface poisoning (presence of chloride, sulfides, humic acid (HA)), and regeneration of Cu(0) sites on catalytic dechlorination of aqueous-phase 1,2-dichloroethane (1,2-DCA) via nCu(0)-borohydride. Scanning electron microscopy confirmed the nano size and quasi-spherical shape of nCu(0) particles. X-ray diffraction confirmed the presence of Cu(0) and Cu(2)O and x-ray photoelectron spectroscopy also provided the Cu(0)/Cu(n+) ratios. Reactivity experiments showed that nCu(0) was incapable of utilizing H(2) from borohydride left over during nCu(0) synthesis and, hence, additional borohydride was essential for 1,2-DCA dechlorination. Washing the nCu(0) particles improved their Cu(0)/Cu(n+) ratio (1.27) and 92% 1,2-DCA was removed in 7 h with k(obs) = 0.345 h(−1) as compared to only 44% by unwashed nCu(0) (0.158 h(−1)) with Cu(0)/Cu(n+) ratio of 0.59, in the presence of borohydride. The presence of chloride (1000–2000 mg L(−1)), sulfides (0.4–4 mg L(−1)), and HA (10–30 mg L(−1)) suppressed 1,2-DCA dechlorination; which was improved by additional borohydride probably via regeneration of Cu(0) sites. Coating the particles decreased their catalytic dechlorination efficiency. 85–90% of the removed 1,2-DCA was recovered as chloride. Chloroethane and ethane were main dechlorination products indicating hydrogenolysis as the major pathway. Our results imply that synthesis parameters and groundwater solutes control nCu(0) catalytic activity by altering its physico-chemical properties. Thus, these factors should be considered to develop an efficient remedial design for practical applications of nCu(0)-borohydride. Nature Publishing Group UK 2023-07-23 /pmc/articles/PMC10363550/ /pubmed/37482593 http://dx.doi.org/10.1038/s41598-023-38678-6 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 Boparai, Hardiljeet Kaur El-Sharnouby, Omneya O’Carroll, Denis M. Catalytic dechlorination of 1,2-DCA in nano Cu(0)-borohydride system: effects of Cu(0)/Cu(n+) ratio, surface poisoning, and regeneration of Cu(0) sites |
title | Catalytic dechlorination of 1,2-DCA in nano Cu(0)-borohydride system: effects of Cu(0)/Cu(n+) ratio, surface poisoning, and regeneration of Cu(0) sites |
title_full | Catalytic dechlorination of 1,2-DCA in nano Cu(0)-borohydride system: effects of Cu(0)/Cu(n+) ratio, surface poisoning, and regeneration of Cu(0) sites |
title_fullStr | Catalytic dechlorination of 1,2-DCA in nano Cu(0)-borohydride system: effects of Cu(0)/Cu(n+) ratio, surface poisoning, and regeneration of Cu(0) sites |
title_full_unstemmed | Catalytic dechlorination of 1,2-DCA in nano Cu(0)-borohydride system: effects of Cu(0)/Cu(n+) ratio, surface poisoning, and regeneration of Cu(0) sites |
title_short | Catalytic dechlorination of 1,2-DCA in nano Cu(0)-borohydride system: effects of Cu(0)/Cu(n+) ratio, surface poisoning, and regeneration of Cu(0) sites |
title_sort | catalytic dechlorination of 1,2-dca in nano cu(0)-borohydride system: effects of cu(0)/cu(n+) ratio, surface poisoning, and regeneration of cu(0) sites |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10363550/ https://www.ncbi.nlm.nih.gov/pubmed/37482593 http://dx.doi.org/10.1038/s41598-023-38678-6 |
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