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DOI 10.1016/j.chemosphere.2021.130020

Медицинская библиотека · Chemosphere · 2021

Synthesis and NOx removal performance of anatase S-TiO2/g-CN heterojunction formed from dye wastewater sludge.

Hossain Sayed Mukit, Park Heeju, Kang Hui-Ju, Mun Jong Seok, Tijing Leonard, Rhee Inkyu, Kim Jong-Ho, Jun Young-Si, Shon Ho Kyong

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Аннотация

In this study, sludges generated from Ti-based flocculation of dye wastewater were used to retrieve photoactive titania (S-TiO2). It was heterojunctioned with graphitic carbon nitride (g-CN) to augment photoactivity under UV/visible light irradiance. Later the as-prepared samples were utilized to remove nitrogen oxides (NOx) in the atmospheric condition through photocatalysis. Heterojunction between S-TiO2 and g-CN was prepared through facile calcination (@550 °C) of S-TiO2 and melamine mix. Advanced sample characterization was carried out and documented extensively. Successful heterojunction was confirmed from the assessment of morphological and optical attributes of the samples. Finally, the prepared samples' level of photoactivity was assessed through photooxidation of NOx under both UV and visible light irradiance. Enhanced photoactivity was observed in the prepared samples irrespective of the light types. After 1 h of UV/visible light-based photooxidation, the best sample STC4 was found to remove 15.18% and 9.16% of atmospheric NO, respectively. In STC4, the mixing ratio of S-TiO2, to melamine was maintained as 1:3. Moreover, the optical bandgap of STC4 was found as 2.65 eV, where for S-TiO2, it was 2.83 eV. Hence, the restrained rate of photogenerated charge recombination and tailored energy bandgap of the as-prepared samples were the primary factors for enhancing photoactivity.

Для цитирования: Hossain Sayed Mukit, Park Heeju, Kang Hui-Ju, Mun Jong Seok, Tijing Leonard, Rhee Inkyu, Kim Jong-Ho, Jun Young-Si, Shon Ho Kyong. Synthesis and NOx removal performance of anatase S-TiO2/g-CN heterojunction formed from dye wastewater sludge.. Chemosphere. 2021. DOI: 10.1016/j.chemosphere.2021.130020.

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