Mesoporous and adsorption behavior of algal biochar prepared via sequential hydrothermal carbonization and ZnCl2 activation

[Display omitted] •Brown algal was hydrothermally carbonized to modify surface physicochemistry.•ZnCl2-activated hydrochar produced mesoporous biochar.•Algal biochar showed superior ciprofloxacin removal in different conditions.•Electrostatic interaction, H-bond and π-EDA were major adsorption mecha...

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Veröffentlicht in:Bioresource technology 2022-02, Vol.346, p.126351-126351, Article 126351
Hauptverfasser: Nguyen, Thanh-Binh, Truong, Quoc-Minh, Chen, Chiu-Wen, Doong, Ruey-an, Chen, Wei-Hsin, Dong, Cheng-Di
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container_end_page 126351
container_issue
container_start_page 126351
container_title Bioresource technology
container_volume 346
creator Nguyen, Thanh-Binh
Truong, Quoc-Minh
Chen, Chiu-Wen
Doong, Ruey-an
Chen, Wei-Hsin
Dong, Cheng-Di
description [Display omitted] •Brown algal was hydrothermally carbonized to modify surface physicochemistry.•ZnCl2-activated hydrochar produced mesoporous biochar.•Algal biochar showed superior ciprofloxacin removal in different conditions.•Electrostatic interaction, H-bond and π-EDA were major adsorption mechanism. In this study, biochar derived from brown algal Ascophyllum nodosum was synthesized through hydrothermal carbonization (HTC) coupling with ZnCl2 chemical activation and applied as a sustainable adsorbent for antibiotic removal from water exemplified by ciprofloxacin (CIP). Various surface analysis techniques such as Brunauer-Emmett-Teller (BET), scanning electron microscopy (SEM), Fourier transform infrared (FTIR) spectroscopy, and zeta potential were used to clarify the surface properties of prepared biochars. The adsorption performance of biochars was investigated using batch adsorption experiments with a variety of parameters (initial pH, ionic types, temperature and water matrixes). The application of prepared biochar in CIP removal showed a good result of adsorption capacity (150–400 mg g−1) in different conditions. Overall, algal biochars, as a product recycled from biowaste, demonstrated a novel and promising adsorbent for effective and sustainable method for removal of antibiotics from water.
doi_str_mv 10.1016/j.biortech.2021.126351
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In this study, biochar derived from brown algal Ascophyllum nodosum was synthesized through hydrothermal carbonization (HTC) coupling with ZnCl2 chemical activation and applied as a sustainable adsorbent for antibiotic removal from water exemplified by ciprofloxacin (CIP). Various surface analysis techniques such as Brunauer-Emmett-Teller (BET), scanning electron microscopy (SEM), Fourier transform infrared (FTIR) spectroscopy, and zeta potential were used to clarify the surface properties of prepared biochars. The adsorption performance of biochars was investigated using batch adsorption experiments with a variety of parameters (initial pH, ionic types, temperature and water matrixes). The application of prepared biochar in CIP removal showed a good result of adsorption capacity (150–400 mg g−1) in different conditions. 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In this study, biochar derived from brown algal Ascophyllum nodosum was synthesized through hydrothermal carbonization (HTC) coupling with ZnCl2 chemical activation and applied as a sustainable adsorbent for antibiotic removal from water exemplified by ciprofloxacin (CIP). Various surface analysis techniques such as Brunauer-Emmett-Teller (BET), scanning electron microscopy (SEM), Fourier transform infrared (FTIR) spectroscopy, and zeta potential were used to clarify the surface properties of prepared biochars. The adsorption performance of biochars was investigated using batch adsorption experiments with a variety of parameters (initial pH, ionic types, temperature and water matrixes). The application of prepared biochar in CIP removal showed a good result of adsorption capacity (150–400 mg g−1) in different conditions. 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subjects Adsorption
Algal biochar
Ciprofloxacin (CIP)
Hydrothermal carbonization
ZnCl2
title Mesoporous and adsorption behavior of algal biochar prepared via sequential hydrothermal carbonization and ZnCl2 activation
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