Waste-Based Ceramsite for the Efficient Removal of Ciprofloxacin in Aqueous Solutions

Author:

Qin Juan1,Fang Yeting1,Shi Jian2,Tokoro Chiharu34ORCID,Córdova-Udaeta Mauricio3ORCID,Oyama Keishi3,Zhang Juncheng5

Affiliation:

1. Nantong Key Laboratory of Intelligent and New Energy Materials, School of Chemistry and Chemical Engineering, Nantong University, Nantong 226019, China

2. Analysis and Testing Center, Nantong University, Nantong 226019, China

3. Faculty of Science and Engineering, Waseda University, 3-4-1 Okubo, Shinjuku-ku, Tokyo 169-8555, Japan

4. Faculty of Engineering, University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8656, Japan

5. Department of Science and Engineering, Aoyama Gakuin University, Sagamihara 252-5258, Japan

Abstract

Ciprofloxacin (CIP), a compound with bioaccumulation toxicity and antibiotic resistance, is frequently detected in water at alarming concentrations, which is becoming an increasing concern. In this study, a low-cost ceramsite was developed from industrial solid wastes through sintering to remove CIP from wastewater. The effects of adsorbent dosage, initial pH, contact time, initial CIP concentration, and temperature were explored. More than 99% of CIP (20–60 mg/L) was removed at around pH 2–4 by the ceramsite. The kinetic data fitted well with the pseudo-second-order model, revealing that chemisorption was the main rate-determining step. The isotherm data was better described by the Freundlich model, suggesting that CIP was removed by the formation of multiple layers on the heterogeneous surface. Moreover, the removal efficiency was practically higher than 95% during five regeneration cycles, when different regeneration methods were used, including calcination, HCl, and NaOH washing, indicating that the ceramsite exhibited outstanding reusability in removing CIP. The primary mechanism of CIP removal by the ceramsite was found to be the synergism of adsorption and flocculation, both of which depended on the release of Ca2+ from the ceramsite. In addition, strong Ca-CIP complexes could be formed through surface complexation and metal cation bridging between Ca2+ and different functional groups in CIP.

Funder

the National Natural Science Foundation of China

the Natural Science Foundation of Jiangsu Province

the Jiangsu Water Conservancy Science and Technology project

Publisher

MDPI AG

Subject

Health, Toxicology and Mutagenesis,Public Health, Environmental and Occupational Health

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