کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
6466669 1422965 2017 11 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Direct fabrication of lamellar self-supporting Co3O4/N/C peroxymonosulfate activation catalysts for effective aniline degradation
موضوعات مرتبط
مهندسی و علوم پایه مهندسی شیمی مهندسی شیمی (عمومی)
پیش نمایش صفحه اول مقاله
Direct fabrication of lamellar self-supporting Co3O4/N/C peroxymonosulfate activation catalysts for effective aniline degradation
چکیده انگلیسی


- Lamellar self-supporting Co3O4/N/C were fabricated directly.
- Co3O4/N/C is an efficient heterogeneous catalyst for activation of PMS.
- Favorable catalytic properties own to the formation of highly active N-binding metal sites.

N-doped carbon materials have great potential as functional materials for water pollution control. However, the synthesis of green and sustainable N-doped carbon catalysts face numerous challenges. This study uses a thermal treatment by directly heating a homogeneous mixture of cobalt acetate and dimethylglyoxime to synthesize lamellar ordering Co3O4/N/C compounds. Dimethylglyoxime was chosen to play duple roles as both nitrogen and carbon source. The obtained N-doped carbon material was used as a catalyst for effective aniline degradation by activating peroxymonosulfate (PMS). In this approach, nanomaterials with good catalytic performance, high stability, and magnetic property can be obtained, which facilitate recycle convenience. In this study, graphitic N is found to improve electron mobility, and the lone pair of pyrrolic-like N electrons tends to form effective Co-N4 moieties with Co species, which can increase the catalyst activity. Therefore, the prepared catalyst has higher activity than individual Co3O4. Furthermore, the effects of N-doped carbon materials on aniline degradation by activated PMS and the proposed reaction pathways for the mineralization of aniline were explain in detailed.

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ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Chemical Engineering Journal - Volume 313, 1 April 2017, Pages 1088-1098
نویسندگان
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