ISSN: 0256-1115 (print version) ISSN: 1975-7220 (electronic version)
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In relation to this article, we declare that there is no conflict of interest.
Publication history
Received February 21, 2026
Accepted May 26, 2026
Available online October 25, 2026
articles This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/bync/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
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Most Cited

Montmorillonite-Loaded Copper Sulfide for the Removal of Tetracycline Hydrochloride from Aqueous Solutions

College of Science, Nanjing Agricultural University
zhangfan0128@njau.edu.cn
Korean Journal of Chemical Engineering, October 2026, 43(12), 3285-3298(14)
https://doi.org/10.1007/s11814-026-00761-9

Abstract

Copper sulfide (CuS) is a common catalytic degradation material, but its adsorption performance for tetracycline hydrochloride

(TCH) remains insufficiently studied. In this work, a modified CuS material was developed for the adsorption of 

TCH in water. Montmorillonite (MMT) was employed as a carrier to enhance the dispersion of CuS, resulting in the synthesis

of montmorillonite-loaded CuS (CuS@MMT). Comprehensive characterization revealed that the composite material 

exhibited a block-like morphology with nanoflower clusters anchored on the supports, demonstrating good crystallinity 

and a structure comprising hexagonal CuS and montmorillonite phases. The (001) diffraction peak of the composite shifted 

compared to the standard MMT reference, indicating an expanded interlayer spacing of montmorillonite and successful 

intercalation of CuS into the interlayers, which effectively dispersed CuS particles. During the purification process, the 

leaching concentration of Cu ions was measured at 1.6 mg·L−1

, demonstrating minimal secondary contamination. Adsorption

kinetics followed the pseudo-second-order kinetic model, suggesting chemisorption as the rate-limiting step. Isothermal

adsorption data aligned with the Langmuir model, confirming monolayer adsorption. A response surface methodology 

(RSM) based on the Doehlert matrix (DM) was employed for mathematical modeling and optimization, yielding optimal 

adsorption conditions: adsorbent dosage of 0.08 g, initial TCH concentration of 20 mg·L−1

, and pH 6.5, achieving a 100% 

removal efficiency. Recyclability tests showed that the material maintained an adsorption capacity of 24.16 mg·g−1

 after 

five cycles. Among coexisting anions, CO3

2− exerted the most significant inhibitory effect on TCH adsorption, while Cl−

and SO4

2− showed minor impacts. Remarkably, the material exhibited high adsorption capacities exceeding 151 mg·g−1

 for 

TCH in real water matrices, including tap water, Xuanwu Lake water, and Yangtze River water, highlighting its practical 

applicability in natural aqueous environments.

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