Xian Zhang, Ze Liu, Hafiz Ihsan Ul Haq Khan, Diederik P L Rousseau, Stijn Van Hulle
{"title":"可持续炭化氢作为一种高效的过硫酸盐活化剂,可经济有效地降解双酚 A。","authors":"Xian Zhang, Ze Liu, Hafiz Ihsan Ul Haq Khan, Diederik P L Rousseau, Stijn Van Hulle","doi":"10.1016/j.chemosphere.2024.143262","DOIUrl":null,"url":null,"abstract":"<p><p>This study explored Mason pine-derived hydrochar (MPHC) as an effective adsorbent and persulfate (PS) activator for degrading bisphenol A (BPA). Increasing MPHC dosage from 0.25 to 2.0 g L<sup>-1</sup> raised BPA removal from 42% to 87%. Similarly, at the same MPHC dosage range and fixed PS concentration (8 mM), BPA removal by MPHC/PS increased from 66% to 91%. Additionally, at a fixed MPHC dosage (1.0 g L<sup>-1</sup>), higher PS concentrations (2-32 mM) resulted in an overall BPA removal increase from 78% to 99%. The optimal pH for BPA removal by MPHC was at pH 3, while for MPHC/PS was at pH 9. BPA degradation by MPHC was optimal at pH 3, whereas MPHC/PS was at pH 3 and pH 9. Additionally, pH 7 favored BPA adsorption for both MPHC and MPHC/PS. The study also considered the influence of coexisting anions and humic acid (HA). PO<sub>4</sub><sup>3-</sup> and NO<sub>3</sub><sup>-</sup> influence adsorption on MPHC, but these anions' effect on MPHC/PS is limited. Furthermore, the existence of HA had minimal influence on BPA removal by MPHC/PS. The contributions of different reactive species by MPHC for BPA degradation are as follows: electron-hole (h<sup>+</sup>) 2%, singlet oxygen (<sup>1</sup>O<sub>2</sub>) 7%, superoxide radicals (O<sub>2</sub><sup>•-</sup>) 13%, electron (e<sup>-</sup>) 2%, hydroxyl radical (<sup>•</sup>OH) 3%, whereas the remaining 48% removal was the contribution of adsorption. For MPHC/PS, adsorption accounted for 39 %, more reactive species were involved in degradation, and the donations are (h<sup>+</sup>) 3%, sulfate radicals (SO<sub>4</sub><sup>•-</sup>) 3%, (<sup>1</sup>O<sub>2</sub>) 19%, (O<sub>2</sub><sup>•-</sup>) 15%, (e<sup>-</sup>) 2%, and (<sup>•</sup>OH) 2%. Additionally, the performance of MPHC remains stable after three operational cycles. The preparation cost of MPHC is 3.01 € kg<sup>-1</sup>. These results highlight the potential of MPHC as an environmentally friendly material for activating PS and removing organic pollutants, suggesting its promising application in future environmental remediation efforts.</p>","PeriodicalId":93933,"journal":{"name":"Chemosphere","volume":" ","pages":"143262"},"PeriodicalIF":0.0000,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Sustainable hydrochar as an efficient persulfate activator for cost-effective degradation of bisphenol A.\",\"authors\":\"Xian Zhang, Ze Liu, Hafiz Ihsan Ul Haq Khan, Diederik P L Rousseau, Stijn Van Hulle\",\"doi\":\"10.1016/j.chemosphere.2024.143262\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>This study explored Mason pine-derived hydrochar (MPHC) as an effective adsorbent and persulfate (PS) activator for degrading bisphenol A (BPA). Increasing MPHC dosage from 0.25 to 2.0 g L<sup>-1</sup> raised BPA removal from 42% to 87%. Similarly, at the same MPHC dosage range and fixed PS concentration (8 mM), BPA removal by MPHC/PS increased from 66% to 91%. Additionally, at a fixed MPHC dosage (1.0 g L<sup>-1</sup>), higher PS concentrations (2-32 mM) resulted in an overall BPA removal increase from 78% to 99%. The optimal pH for BPA removal by MPHC was at pH 3, while for MPHC/PS was at pH 9. BPA degradation by MPHC was optimal at pH 3, whereas MPHC/PS was at pH 3 and pH 9. Additionally, pH 7 favored BPA adsorption for both MPHC and MPHC/PS. The study also considered the influence of coexisting anions and humic acid (HA). PO<sub>4</sub><sup>3-</sup> and NO<sub>3</sub><sup>-</sup> influence adsorption on MPHC, but these anions' effect on MPHC/PS is limited. Furthermore, the existence of HA had minimal influence on BPA removal by MPHC/PS. The contributions of different reactive species by MPHC for BPA degradation are as follows: electron-hole (h<sup>+</sup>) 2%, singlet oxygen (<sup>1</sup>O<sub>2</sub>) 7%, superoxide radicals (O<sub>2</sub><sup>•-</sup>) 13%, electron (e<sup>-</sup>) 2%, hydroxyl radical (<sup>•</sup>OH) 3%, whereas the remaining 48% removal was the contribution of adsorption. For MPHC/PS, adsorption accounted for 39 %, more reactive species were involved in degradation, and the donations are (h<sup>+</sup>) 3%, sulfate radicals (SO<sub>4</sub><sup>•-</sup>) 3%, (<sup>1</sup>O<sub>2</sub>) 19%, (O<sub>2</sub><sup>•-</sup>) 15%, (e<sup>-</sup>) 2%, and (<sup>•</sup>OH) 2%. Additionally, the performance of MPHC remains stable after three operational cycles. The preparation cost of MPHC is 3.01 € kg<sup>-1</sup>. These results highlight the potential of MPHC as an environmentally friendly material for activating PS and removing organic pollutants, suggesting its promising application in future environmental remediation efforts.</p>\",\"PeriodicalId\":93933,\"journal\":{\"name\":\"Chemosphere\",\"volume\":\" \",\"pages\":\"143262\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-09-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chemosphere\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1016/j.chemosphere.2024.143262\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/9/3 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemosphere","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1016/j.chemosphere.2024.143262","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/9/3 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
本研究探讨了梅森松衍生炭(MPHC)作为一种有效的吸附剂和过硫酸盐(PS)活化剂降解双酚 A(BPA)的问题。将 MPHC 的用量从 0.25 g L-1 提高到 2.0 g L-1,双酚 A 的去除率从 42% 提高到 87%。同样,在相同的 MPHC 用量范围和固定的 PS 浓度(8 mM)下,MPHC/PS 对双酚 A 的去除率从 66% 提高到 91%。此外,在固定的 MPHC 用量(1.0 g L-1)和较高的 PS 浓度(2 至 32 mM)条件下,双酚 A 的总体去除率从 78% 提高到 99%。MPHC 去除双酚 A 的最佳 pH 值为 pH 值 3,而 MPHC/PS 的最佳 pH 值为 pH 值 9。 此外,pH 值 7 对 MPHC 和 MPHC/PS 的双酚 A 吸附均有利。研究还考虑了共存阴离子和腐殖酸(HA)的影响。PO43- 和 NO3- 会影响对 MPHC 的吸附,但这些阴离子对 MPHC/PS 的影响有限。此外,HA 的存在对 MPHC/PS 去除双酚 A 的影响微乎其微。不同活性物种对 MPHC 降解双酚 A 的贡献如下:电子-空穴(h+)2%、单线态氧(1O2)7%、超氧自由基(O2--)13%、电子(e-)2%、羟自由基(-OH)3%,而其余 48% 的去除率是吸附的贡献。对于 MPHC/PS,吸附作用占 39%,更多的反应物参与了降解,其贡献率分别为(h+)3%、硫酸根(SO4--)3%、(1O2)19%、(O2--)15%、(e-)2% 和(-OH)2%。此外,MPHC 的性能在三个运行周期后保持稳定。MPHC 的制备成本为 3.01 欧元 kg-1。这些结果凸显了 MPHC 作为一种环境友好型材料在活化 PS 和去除有机污染物方面的潜力,表明其在未来的环境修复工作中具有广阔的应用前景。
Sustainable hydrochar as an efficient persulfate activator for cost-effective degradation of bisphenol A.
This study explored Mason pine-derived hydrochar (MPHC) as an effective adsorbent and persulfate (PS) activator for degrading bisphenol A (BPA). Increasing MPHC dosage from 0.25 to 2.0 g L-1 raised BPA removal from 42% to 87%. Similarly, at the same MPHC dosage range and fixed PS concentration (8 mM), BPA removal by MPHC/PS increased from 66% to 91%. Additionally, at a fixed MPHC dosage (1.0 g L-1), higher PS concentrations (2-32 mM) resulted in an overall BPA removal increase from 78% to 99%. The optimal pH for BPA removal by MPHC was at pH 3, while for MPHC/PS was at pH 9. BPA degradation by MPHC was optimal at pH 3, whereas MPHC/PS was at pH 3 and pH 9. Additionally, pH 7 favored BPA adsorption for both MPHC and MPHC/PS. The study also considered the influence of coexisting anions and humic acid (HA). PO43- and NO3- influence adsorption on MPHC, but these anions' effect on MPHC/PS is limited. Furthermore, the existence of HA had minimal influence on BPA removal by MPHC/PS. The contributions of different reactive species by MPHC for BPA degradation are as follows: electron-hole (h+) 2%, singlet oxygen (1O2) 7%, superoxide radicals (O2•-) 13%, electron (e-) 2%, hydroxyl radical (•OH) 3%, whereas the remaining 48% removal was the contribution of adsorption. For MPHC/PS, adsorption accounted for 39 %, more reactive species were involved in degradation, and the donations are (h+) 3%, sulfate radicals (SO4•-) 3%, (1O2) 19%, (O2•-) 15%, (e-) 2%, and (•OH) 2%. Additionally, the performance of MPHC remains stable after three operational cycles. The preparation cost of MPHC is 3.01 € kg-1. These results highlight the potential of MPHC as an environmentally friendly material for activating PS and removing organic pollutants, suggesting its promising application in future environmental remediation efforts.