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Title: | Using ZrO<inf>2</inf> coated sludge from drinking water treatment plant as a novel adsorbent for nitrate removal from contaminated water |
Authors: | Huy Hoang Phan Quang Kiet Tuan Phan Nga Thi Dinh Thanh Ngoc Tran Thi Puangrat Kajitvichyanukul Pankaj Raizada Pardeep Singh Van Huy Nguyen |
Authors: | Huy Hoang Phan Quang Kiet Tuan Phan Nga Thi Dinh Thanh Ngoc Tran Thi Puangrat Kajitvichyanukul Pankaj Raizada Pardeep Singh Van Huy Nguyen |
Keywords: | Biochemistry, Genetics and Molecular Biology;Environmental Science |
Issue Date: | 1-Sep-2022 |
Abstract: | This study aimed to produce a novel efficient absorbent using sludge generated from drinking water treatment plants (DWTPs) as a low-cost absorbent and applied to treat nitrate (NO3−) from contaminated water. Before the ZrO2 coating experiment, the drinking water sludge (DWS) from DWTPs was pretreated by thermal treatment (80 °C, 200 °C, and 500 °C). After that, ZrO2 coated drinking water sludge (DWS@ZrO2) was produced by a simple precipitated reaction. The synthesized DWS@ZrO2 was characterized by FTIR, SEM, and EDS with mapping analysis, XRD, and VSM. The results revealed that DWS@ZrO2 could improve the pore filling in the adsorption experiment. The highest nitrate adsorption capacity was achieved (30.99 mg g− 1) at pH 2 with DWS500@ZrO2. Adsorption kinetics indicated that pyrolyzed DWS at 500 °C provided the highest nitrate adsorption capacity, followed by 200 °C, and 80 °C. Thermodynamic results showed that the obtained nitrate removal was an endothermic and spontaneous process. The possible nitrate adsorption mechanism of DWS@ZrO2 could mainly involve pore filling, electrostatic interaction, and ligand exchange. The experimental results suggest that DWS@ZrO2 is a feasible absorbent with high-efficiency, low-cost, high recyclability, and eco-friendly characteristics for treating nitrate in an aqueous solution. |
URI: | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85132438982&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/74477 |
ISSN: | 10960953 00139351 |
Appears in Collections: | CMUL: Journal Articles |
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