اخبار و اعلانات

 آمار

تعداد نشریات418
تعداد شماره‌ها9,991
تعداد مقالات83,502
تعداد مشاهده مقاله76,927,270
تعداد دریافت فایل اصل مقاله53,998,046
Muthuvel, Inbasekaran, Gowthami, Kaliyamoorthy, Thirunarayanan, Ganesamoorthy, Suppuraj, Palusamy, Krishnakumar, Balu, Fraga do Nascimento Sobral, Abílio José, Swaminathan, Meenakshisundaram. (1397). Graphene oxide–Fe2V4O13 hybrid material as highly efficient hetero-Fenton catalyst for degradation of methyl orange. نشریه علمی پژوهشی دانشگاه آزاد اسلامی, 10(1), 77-87. doi: https://doi.org/10.1007/s40090-019-0173-8
Inbasekaran Muthuvel; Kaliyamoorthy Gowthami; Ganesamoorthy Thirunarayanan; Palusamy Suppuraj; Balu Krishnakumar; Abílio José Fraga do Nascimento Sobral; Meenakshisundaram Swaminathan. "Graphene oxide–Fe2V4O13 hybrid material as highly efficient hetero-Fenton catalyst for degradation of methyl orange". نشریه علمی پژوهشی دانشگاه آزاد اسلامی, 10, 1, 1397, 77-87. doi: https://doi.org/10.1007/s40090-019-0173-8
Muthuvel, Inbasekaran, Gowthami, Kaliyamoorthy, Thirunarayanan, Ganesamoorthy, Suppuraj, Palusamy, Krishnakumar, Balu, Fraga do Nascimento Sobral, Abílio José, Swaminathan, Meenakshisundaram. (1397). 'Graphene oxide–Fe2V4O13 hybrid material as highly efficient hetero-Fenton catalyst for degradation of methyl orange', نشریه علمی پژوهشی دانشگاه آزاد اسلامی, 10(1), pp. 77-87. doi: https://doi.org/10.1007/s40090-019-0173-8
Muthuvel, Inbasekaran, Gowthami, Kaliyamoorthy, Thirunarayanan, Ganesamoorthy, Suppuraj, Palusamy, Krishnakumar, Balu, Fraga do Nascimento Sobral, Abílio José, Swaminathan, Meenakshisundaram. Graphene oxide–Fe2V4O13 hybrid material as highly efficient hetero-Fenton catalyst for degradation of methyl orange. نشریه علمی پژوهشی دانشگاه آزاد اسلامی, 1397; 10(1): 77-87. doi: https://doi.org/10.1007/s40090-019-0173-8

Graphene oxide–Fe2V4O13 hybrid material as highly efficient hetero-Fenton catalyst for degradation of methyl orange

International Journal of Industrial Chemistry
دوره 10، شماره 1، خرداد 2019، صفحه 77-87
نوع مقاله: research article
شناسه دیجیتال (DOI): https://doi.org/10.1007/s40090-019-0173-8
نویسندگان
Inbasekaran Muthuvel* 1، 2؛ Kaliyamoorthy Gowthami3؛ Ganesamoorthy Thirunarayanan3؛ Palusamy Suppuraj3؛ Balu Krishnakumar4؛ Abílio José Fraga do Nascimento Sobral4؛ Meenakshisundaram Swaminathan5
1Advanced Photocatalysis Laboratory, Department of Chemistry, Annamalai University, Annamalainagar, Tamilnadu 608 002, India
2Photocatalysis Laboratory, Department of Chemistry, M.R. Govt. Arts College, Mannargudi, Tamilnadu 614 001, India
3Advanced Photocatalysis Laboratory, Department of Chemistry, Annamalai University, Annamalainagar, Tamilnadu, 608 002, India
4Department of Chemistry, University of Coimbra, 3004-535, Coimbra, Portugal
5Nanomaterials Laboratory, International Research Centre, Kalasalingam University, Krishnankoil, Tamilnadu, 626 126, India
چکیده
A new hetero-Fenton type GO/Fe2V4O13 was developed and characterized by FT-IR, XRD, HR-SEM, TEM, and UV-DRS analysis. XRD pattern reveals the presence of monoclinic phase of Fe2V4O13 in the catalyst. TEM images show the particle sizes in the range from 20 to 100 nm and the nice dispersion of nanosized Fe2V4O13 particles on the surface of the graphene oxide. The hetero-Fenton catalyst was used for the degradation of Methyl orange (MO) under UV and solar light. The mineralization rate was influenced by H2O2 concentration, pH, and catalyst loading. The reusability 21% GO/Fe2V4O13 was analyzed. GO/Fe2V4O13 was stable and reusable up to five cycles with 95% degradation. Solar experiments were carried out at different initial solution pH with Fe2V4O13 and 21% GO/Fe2V4O13. Both catalysts show maximum degradation efficiency at pH 6. Mechanism of heterophoto-Fenton process is also proposed. This study reveals that Fe2V4O13 and 21% GO/Fe2V4O13 catalysts are efficient under UV and solar light for the degradation MO and can be utilized for the treatment of dye wastewater.
کلیدواژه‌ها
Fe2V4O13 · Graphene oxide · Wastewater treatment · Hetero؛ Fenton reaction · Photocatalysis
آمار
تعداد مشاهده مقاله: 44


سامانه مدیریت نشریات علمی. قدرت گرفته از سیناوب