Overall
- Language
- English
- Conflict of Interest
- 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
-
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.
Most Cited
Montmorillonite-Loaded Copper Sulfide for the Removal of Tetracycline Hydrochloride from Aqueous Solutions
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.

