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  4. Process-intensified synthesis of sulfonated peanut shell char through dilute acid hydrolysis and low-temperature sulfonation–carbonization for Pb2 + removal
 
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Process-intensified synthesis of sulfonated peanut shell char through dilute acid hydrolysis and low-temperature sulfonation–carbonization for Pb2 + removal

Journal
Journal of Environmental Chemical Engineering
Journal Volume
14
Journal Issue
3
Start Page
122446
ISSN
22132929
Date Issued
2026-06
Author(s)
Stefani, Maria
Cheng, Kuan-Chen  
Veronica, Theresia Angeline
Ernest, Edward Hartman
et al.
DOI
10.1016/j.jece.2026.122446
URI
https://www.scopus.com/pages/publications/105034377032
https://scholars.lib.ntu.edu.tw/handle/123456789/737650
Abstract
Lead (Pb2+) contamination in water poses persistent environmental and public health risks, driving the need for efficient and sustainable treatment technologies. In this study, a process-intensified and low-energy route is developed to valorize peanut shell waste into a high-performance sulfonated carbon adsorbent via an integrated dilute acid hydrolysis and simultaneous sulfonation–partial carbonization (DAH–SS-PC) strategy. The DAH step partially hydrolyzes the lignocellulosic matrix while generating a sugar-rich hydrolysate as a value-added co-product and retaining a reactive solid precursor. Subsequent low-temperature SS-PC treatment (80–120 °C) introduces sulfonic and oxygen-containing functional groups, yielding a chemically heterogeneous surface enriched with coordination-active sites. The optimized SPS-Char exhibits a high Pb²⁺ adsorption capacity of 3126.9 mg/g, while sigmoidal modeling yields an apparent asymptotic capacity of 3711.9 mg/g. The adsorption behavior deviates from classical monolayer models and follows a sigmoidal isotherm, indicating cooperative, multi-site adsorption driven by heterogeneous surface chemistry. Kinetic analysis reveals pseudo-second-order behavior, consistent with coordination-driven adsorption. Spectroscopic evidence (FTIR and XPS) confirms the involvement of sulfonic and oxygen-containing groups in Pb2+ binding through surface complexation. The adsorbent maintains high removal efficiency under competitive ionic conditions, highlighting its selectivity and robustness in complex aqueous environments. This work establishes a clear structure–function relationship linking low-temperature synthesis, surface chemical heterogeneity, and cooperative adsorption, offering a scalable and energy-efficient pathway for advanced heavy metal remediation.
Subjects
Biomass waste valorization
Heavy metal adsorption
Low-temperature sulfonated carbon
Pb2+ removal
Process intensification
Publisher
Elsevier BV
Description
Article number 122446
Type
journal article

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