{"title":"Temperature-tailored cellulose-rich Cladophora sp. hydrochar for selective malachite green adsorption from multi-dye systems","authors":"Muhammad Badaruddin , Laila Hanum , Elda Melwita , Sahrul Wibiyan , Yulizah Hanifah , Aldes Lesbani","doi":"10.1016/j.bej.2025.109986","DOIUrl":null,"url":null,"abstract":"<div><div>This study presents the selective adsorption of malachite green (MG) from multi-dye mixtures using hydrochar derived from <em>Cladophora</em> sp<em>.</em> (C) via hydrothermal carbonization (HTC) at 150°C (C150), 200°C (C200), 250°C (C250), and 300°C (C300). Structural characterizations (XRD, FTIR, SEM-EDS, BET) confirmed enhanced porosity and surface functionalization with increasing HTC temperature. C200 exhibited the highest BET surface area (15.84 m²/g), while C300, with the largest pore size (18.27 nm), showed the highest MG adsorption capacity (204.1 mg/g), outperforming C (30.03 mg/g). Selective adsorption tests using ternary anionic-cationic dye mixtures revealed strong affinity toward cationic dyes, with MG showing 95.5 % removal by C300. Kinetic studies fitted the pseudo-second-order model, suggesting chemisorption dominance; the Avrami model also correlated well. Increasing Avrami rate constant (k₃) and decreasing exponent (n) with HTC temperature indicate a transition from diffusion to surface-controlled chemisorption. Equilibrium data followed the Sips isotherm, reflecting mixed monolayer–multilayer adsorption on moderately heterogeneous surfaces. The rising Sips constant (Kₛ) with temperature confirmed an endothermic process consistent with thermodynamic findings, which also verified spontaneity. Regeneration studies showed C300 retained > 50 % efficiency after three cycles, demonstrating stability and reusability. FTIR, XRD, and XPS analyses before and after MG adsorption confirmed interactions via electrostatic attraction, hydrogen bonding, and π–π interactions.</div></div>","PeriodicalId":8766,"journal":{"name":"Biochemical Engineering Journal","volume":"226 ","pages":"Article 109986"},"PeriodicalIF":3.6000,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biochemical Engineering Journal","FirstCategoryId":"5","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1369703X25003602","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/10/30 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
This study presents the selective adsorption of malachite green (MG) from multi-dye mixtures using hydrochar derived from Cladophora sp. (C) via hydrothermal carbonization (HTC) at 150°C (C150), 200°C (C200), 250°C (C250), and 300°C (C300). Structural characterizations (XRD, FTIR, SEM-EDS, BET) confirmed enhanced porosity and surface functionalization with increasing HTC temperature. C200 exhibited the highest BET surface area (15.84 m²/g), while C300, with the largest pore size (18.27 nm), showed the highest MG adsorption capacity (204.1 mg/g), outperforming C (30.03 mg/g). Selective adsorption tests using ternary anionic-cationic dye mixtures revealed strong affinity toward cationic dyes, with MG showing 95.5 % removal by C300. Kinetic studies fitted the pseudo-second-order model, suggesting chemisorption dominance; the Avrami model also correlated well. Increasing Avrami rate constant (k₃) and decreasing exponent (n) with HTC temperature indicate a transition from diffusion to surface-controlled chemisorption. Equilibrium data followed the Sips isotherm, reflecting mixed monolayer–multilayer adsorption on moderately heterogeneous surfaces. The rising Sips constant (Kₛ) with temperature confirmed an endothermic process consistent with thermodynamic findings, which also verified spontaneity. Regeneration studies showed C300 retained > 50 % efficiency after three cycles, demonstrating stability and reusability. FTIR, XRD, and XPS analyses before and after MG adsorption confirmed interactions via electrostatic attraction, hydrogen bonding, and π–π interactions.
期刊介绍:
The Biochemical Engineering Journal aims to promote progress in the crucial chemical engineering aspects of the development of biological processes associated with everything from raw materials preparation to product recovery relevant to industries as diverse as medical/healthcare, industrial biotechnology, and environmental biotechnology.
The Journal welcomes full length original research papers, short communications, and review papers* in the following research fields:
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Bioseparations including scale-up and protein refolding/renaturation
Environmental Bioengineering including bioconversion, bioremediation, and microbial fuel cells
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Bioresources and Biorefinery Engineering including biomass conversion, biofuels, bioenergy, and optimization
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Metabolic Engineering, Systems and Synthetic Biology including OMICS, bioinformatics, in silico biology, and metabolic flux analysis
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