Magnesium oxide nanoparticles modified biochar derived from tea wastes for enhanced adsorption of o-chlorophenol from industrial wastewater

In this work, magnesium oxide nanoparticles supported biochar derived from tea wastes (MgO@TBC) was prepared as an effective adsorbent for removing hazardous o-chlorophenol (o-CP) from industrial wastewater. The surface area, porous structure, surface functional groups and surface charge of tea wast...

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Published inChemosphere (Oxford) Vol. 337; p. 139342
Main Authors Chu, Thi Thu Hien, Tran, Thi Minh Nguyet, Pham, Minh Thuy, Viet, Nguyen Minh, Thi, Huong Pham
Format Journal Article
LanguageEnglish
Published England Elsevier Ltd 01.10.2023
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Summary:In this work, magnesium oxide nanoparticles supported biochar derived from tea wastes (MgO@TBC) was prepared as an effective adsorbent for removing hazardous o-chlorophenol (o-CP) from industrial wastewater. The surface area, porous structure, surface functional groups and surface charge of tea waste biochar (TBC) significantly enhanced after the modification process. The best uptake performance of o-CP was found at pH = 6.5 and 0.1 g of MgO@TBC adsorbent. According to the adsorption isotherm, the adsorption of o-CP onto MgO@TBC followed the Langmuir model with a maximum uptake capacity of 128.7 mg/g, which was 26.5% higher than TBC (94.6 mg/g). MgO@TBC could be reused for eight cycles with a high o-CP uptake performance (over 60%). Besides, it also exhibited good removal performance of o-CP from industrial wastewater with a removal rate of 81.7%. The adsorption behaviors of o-CP onto MgO@TBC are discussed based on the experimental results. This work may provide information to prepare an effective adsorbent for removing hazardous organic contaminants in wastewater. [Display omitted] •MgO modified biochar derived from tea wastes (MgO@TBC) was prepared.•Removal of o-chlorophenol by MgO@TBC was investigated.•Maximum adsorption capacity of o-chlorophenol was 128.7 mg/g.•81.7% o-chlorophenol was removed from industrial wastewater.
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ISSN:0045-6535
1879-1298
DOI:10.1016/j.chemosphere.2023.139342