Green Synthesis of CHA Zeolite from Expanded Perlite Waste for Rapid and Selective Pb2+ and Cd2+ Removal

The increasing release of non-biodegradable heavy metals, particularly lead (Pb2+) and cadmium (Cd2+), poses severe risks to ecosystems and human health. Herein, we present a sustainable “treating-waste-with-waste” strategy that simultaneously addresses heavy-metal contamination in water and the accumulation of expanded perlite waste. Expanded perlite waste was directly converted into a high-purity, low-silica CHA zeolite via a simple, one-pot, template-free hydrothermal conversion. The resulting sodium-exchanged material (Na-CHA-p) demonstrated excellent Pb2+ and Cd2+ removal performance, featuring ultrafast adsorption kinetics (reaching equilibrium within 5 min for both ions), high adsorption capacities (555.6 mg·g−1 for Pb2+ and 211.0 mg·g−1 for Cd2+), and superior selectivity. This study demonstrates an efficient pathway for the high-value utilization of perlite waste and highlights the strong potential of waste-derived CHA zeolites as advanced adsorbents for heavy-metal wastewater remediation.

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Publication Details

Journal
Molecules
Published
2026-04-22
DOI
https://doi.org/10.3390/molecules31091377
Primary Topic
Adsorption and biosorption for pollutant removal
Type
article
Field-Weighted Citation Impact
0.00

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article

Green Synthesis of CHA Zeolite from Expanded Perlite Waste for Rapid and Selective Pb2+ and Cd2+ Removal

Wenfu Yan, Binyu Wang, Haitao Zhang, Pan Xu et al.
Molecules
Adsorption and biosorption for pollutant removal
article

Green Synthesis of CHA Zeolite from Expanded Perlite Waste for Rapid and Selective Pb2+ and Cd2+ Removal

Wenfu Yan, Binyu Wang, Haitao Zhang, Pan Xu, Z S Liang, Jiaojiao Lv, Changchang Fan
article en

Abstract

The increasing release of non-biodegradable heavy metals, particularly lead (Pb2+) and cadmium (Cd2+), poses severe risks to ecosystems and human health. Herein, we present a sustainable “treating-waste-with-waste” strategy that simultaneously addresses heavy-metal contamination in water and the accumulation of expanded perlite waste. Expanded perlite waste was directly converted into a high-purity, low-silica CHA zeolite via a simple, one-pot, template-free hydrothermal conversion. The resulting sodium-exchanged material (Na-CHA-p) demonstrated excellent Pb2+ and Cd2+ removal performance, featuring ultrafast adsorption kinetics (reaching equilibrium within 5 min for both ions), high adsorption capacities (555.6 mg·g−1 for Pb2+ and 211.0 mg·g−1 for Cd2+), and superior selectivity. This study demonstrates an efficient pathway for the high-value utilization of perlite waste and highlights the strong potential of waste-derived CHA zeolites as advanced adsorbents for heavy-metal wastewater remediation.

MoleculesVol. 31(9)
Jilin University (CN), Chinese Academy of Sciences (CN), Changchun Institute of Optics, Fine Mechanics and Physics (CN), University of Chinese Academy of Sciences (CN), State Key Laboratory of Inorganic Synthesis and Preparative Chemistry
National Natural Science Foundation of China, National Key Research and Development Program of China, Overseas Expertise Introduction Center for Discipline Innovation of Food Nutrition and Human Health (111 Center)
Responsible consumption and production
Openalex Percentile: Top 12%
Adsorption and biosorption for pollutant removal
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Green Synthesis of CHA Zeolite from Expanded Perlite Waste for Rapid and Selective Pb2+ and Cd2+ Removal — Wenfu Yan, Binyu Wang, et al. · Molecules (2026) | TGRS Research Map | TGRS