Surface Charge and Phosphorus Retention in Metal-Activated Biochars from Different Pyrolysis Temperatures

Biochar is a promising material for phosphorus (P) removal from water, but its surface chemistry can limit adsorption efficiency. In this study, biochars produced at 440 °C and 880 °C from the same feedstock were functionalized post-pyrolysis using aqueous solutions of AlCl3, CaCl2, and FeCl3 at two concentrations (0.5 M and 2.0 M). The aim of this work was to assess how both pyrolysis temperature and post-pyrolysis activation with different metals affect the surface charge of biochar and its capacity to retain P from aqueous solution. The treated materials were characterized for pH, point of zero charge (pHpzc), and phosphorus retention from solution. Results showed that Al- and Fe-activation significantly reduced the biochar pH and shifted the pHpzc to more acidic values, enhancing electrostatic attraction toward phosphate species. Phosphorus adsorption was most effective for biochar obtained at 440 °C and treated with AlCl3 and FeCl3, achieving up to 10.2 mg P g−1. These findings highlight the importance of surface charge modulation in tuning biochar performance for phosphate removal from aqueous solution. Based on the obtained results, electrostatic attraction was the main mechanism by which activated biochar adsorbed P from aqueous solution.

Authors

Institutions

Publication Details

Journal
Applied Sciences
Published
2025-08-11
DOI
https://doi.org/10.3390/app15168855
Primary Topic
Phosphorus and nutrient management
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Surface Charge and Phosphorus Retention in Metal-Activated Biochars from Different Pyrolysis Temperatures

Pellegrino Conte, Vito Armando Laudicina, Luigi Badalucco, Sofia Maria Muscarella
4 links
Applied Sciences
Phosphorus and nutrient management
article

Surface Charge and Phosphorus Retention in Metal-Activated Biochars from Different Pyrolysis Temperatures

Pellegrino Conte, Vito Armando Laudicina, Luigi Badalucco, Sofia Maria Muscarella
article en

Abstract

Biochar is a promising material for phosphorus (P) removal from water, but its surface chemistry can limit adsorption efficiency. In this study, biochars produced at 440 °C and 880 °C from the same feedstock were functionalized post-pyrolysis using aqueous solutions of AlCl3, CaCl2, and FeCl3 at two concentrations (0.5 M and 2.0 M). The aim of this work was to assess how both pyrolysis temperature and post-pyrolysis activation with different metals affect the surface charge of biochar and its capacity to retain P from aqueous solution. The treated materials were characterized for pH, point of zero charge (pHpzc), and phosphorus retention from solution. Results showed that Al- and Fe-activation significantly reduced the biochar pH and shifted the pHpzc to more acidic values, enhancing electrostatic attraction toward phosphate species. Phosphorus adsorption was most effective for biochar obtained at 440 °C and treated with AlCl3 and FeCl3, achieving up to 10.2 mg P g−1. These findings highlight the importance of surface charge modulation in tuning biochar performance for phosphate removal from aqueous solution. Based on the obtained results, electrostatic attraction was the main mechanism by which activated biochar adsorbed P from aqueous solution.

Applied SciencesVol. 15(16)
National Interuniversity Consortium of Materials Science and Technology (IT), University of Palermo (IT)
European Commission
Openalex Percentile: Top 75%
Phosphorus and nutrient management
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.