Liming Wu , Zhongyu Su , Jinzhou Fan , Daoguang Teng , Weijun Peng , Wei Wang , Yijun Cao
{"title":"Yeast-activated carbon/montmorillonite nanosheets with porous spherical shells for efficient tetracycline degradation","authors":"Liming Wu , Zhongyu Su , Jinzhou Fan , Daoguang Teng , Weijun Peng , Wei Wang , Yijun Cao","doi":"10.1016/j.clay.2025.107846","DOIUrl":null,"url":null,"abstract":"<div><div>A bio-derived carbon composite catalyst was successfully prepared by loading yeast onto the assembled montmorillonite nanosheets (MMTNS-L), followed by calcination, which effectively prevented catalyst aggregation. MMTNS assembled in a two-dimensional direction to form large sheets, providing a robust support structure. After carbonization, yeast cells, as natural biological entities rich in nitrogen, exhibited a distinctive hollow thin-layer spherical shell with a large specific surface area and abundant pores. The evaporation of internal water vapor further contributed to the formation of this porous structure. The spherical shells uniformly distribute on the assembled MMTNs, resisting aggregation and exposing more active sites, which enhances the catalyst's efficiency. The pyridine N and pyrrole N formed after carbonization provide additional active sites to facilitate electron transfer, while the stable graphite N and N<img>O enhance the catalyst's stability and promote the non-radicals generation. During the degradation process, potassium peroxymonosulfate (PMS) was introduced and activated by the catalyst, generating both free and non-free radicals to effectively degrade tetracycline (TC). Under optimal conditions, the assembly of MMTNS with a lamellar structure, followed by high-temperature yeast carbonization, achieved an 84 % TC degradation rate within 15 min. In this process, <span><math><mo>•</mo><msubsup><mi>SO</mi><mn>4</mn><mo>–</mo></msubsup></math></span>, <span><math><mo>•</mo><msubsup><mi>O</mi><mn>2</mn><mo>–</mo></msubsup></math></span>, and <sup>1</sup>O<sub>2</sub> all participated in TC degradation, with <sup>1</sup>O<sub>2</sub> being the dominant reactive species. As a highly reactive non-radical, <sup>1</sup>O<sub>2</sub> interacts with organic matter to facilitate its degradation. This structure significantly enhances photocatalytic performance and shows great potential for antibiotic removal. This technique aims to enhance the exposure of active sites on carbonized yeast and improve the catalyst's stability, thereby supporting the efficient treatment of antibiotic wastewater and the application of biocarbon catalytic materials.</div></div>","PeriodicalId":245,"journal":{"name":"Applied Clay Science","volume":"273 ","pages":"Article 107846"},"PeriodicalIF":5.3000,"publicationDate":"2025-05-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Applied Clay Science","FirstCategoryId":"89","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0169131725001516","RegionNum":2,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
Abstract
A bio-derived carbon composite catalyst was successfully prepared by loading yeast onto the assembled montmorillonite nanosheets (MMTNS-L), followed by calcination, which effectively prevented catalyst aggregation. MMTNS assembled in a two-dimensional direction to form large sheets, providing a robust support structure. After carbonization, yeast cells, as natural biological entities rich in nitrogen, exhibited a distinctive hollow thin-layer spherical shell with a large specific surface area and abundant pores. The evaporation of internal water vapor further contributed to the formation of this porous structure. The spherical shells uniformly distribute on the assembled MMTNs, resisting aggregation and exposing more active sites, which enhances the catalyst's efficiency. The pyridine N and pyrrole N formed after carbonization provide additional active sites to facilitate electron transfer, while the stable graphite N and NO enhance the catalyst's stability and promote the non-radicals generation. During the degradation process, potassium peroxymonosulfate (PMS) was introduced and activated by the catalyst, generating both free and non-free radicals to effectively degrade tetracycline (TC). Under optimal conditions, the assembly of MMTNS with a lamellar structure, followed by high-temperature yeast carbonization, achieved an 84 % TC degradation rate within 15 min. In this process, , , and 1O2 all participated in TC degradation, with 1O2 being the dominant reactive species. As a highly reactive non-radical, 1O2 interacts with organic matter to facilitate its degradation. This structure significantly enhances photocatalytic performance and shows great potential for antibiotic removal. This technique aims to enhance the exposure of active sites on carbonized yeast and improve the catalyst's stability, thereby supporting the efficient treatment of antibiotic wastewater and the application of biocarbon catalytic materials.
期刊介绍:
Applied Clay Science aims to be an international journal attracting high quality scientific papers on clays and clay minerals, including research papers, reviews, and technical notes. The journal covers typical subjects of Fundamental and Applied Clay Science such as:
• Synthesis and purification
• Structural, crystallographic and mineralogical properties of clays and clay minerals
• Thermal properties of clays and clay minerals
• Physico-chemical properties including i) surface and interface properties; ii) thermodynamic properties; iii) mechanical properties
• Interaction with water, with polar and apolar molecules
• Colloidal properties and rheology
• Adsorption, Intercalation, Ionic exchange
• Genesis and deposits of clay minerals
• Geology and geochemistry of clays
• Modification of clays and clay minerals properties by thermal and physical treatments
• Modification by chemical treatments with organic and inorganic molecules(organoclays, pillared clays)
• Modification by biological microorganisms. etc...