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Although the suitability of some biochars for contaminants' sorption separation has been established, not all potential feedstocks have been explored and characterized. Here, we physicochemically characterized cherry pit biochar (CPB) pyrolyzed from cherry pit biomass (CP) at 500 °C, and we assessed their As and Hg sorption efficiencies in aqueous solutions in comparison to activated carbon (AC). The basic physicochemical and material characterization of the studied adsorbents was carried out using pH, electrical conductivity (EC), cation exchange capacity (CEC), concentration of surface functional groups (Boehm titration), and surface area (SA) analysis; elemental C, H, N analysis; and Fourier-transform infrared spectroscopy (FTIR) and scanning electron microscopy with energy-dispersive X-ray spectroscopy (SEM–EDX). AsO43− anions and Hg2+ cations were selected as model contaminants used to test the sorption properties of the sorption materials. Characterization analyses confirmed a ninefold increase in SA in the case of CPB. The total C concentration increased by 26%, while decreases in the total H and N concentrations were observed. The values of carbonate and ash contents decreased by about half due to pyrolysis processes. The concentrations of surface functional groups of the analyzed biochar obtained by Boehm titration confirmed a decrease in carboxyl and lactone groups, while an increase in phenolic functional groups was observed. Changes in the morphology and surface functionality of the pyrolyzed material were confirmed by SEM–EDX and FTIR analyses. In sorption experiments, we found that the CPB showed better results in the sorption separation of Hg2+ than in the sorption separation of AsO43−. The sorption efficiency for the model cation increased in the order CP < CPB < AC and, for the model anion, it increased in the order CPB < CP < AC. [ABSTRACT FROM AUTHOR]

Elevated or unnatural levels of arsenic (As) and phosphorus (P) concentrations in soils and waterbodies from anthropogenic sources can present significant hazards for both natural ecosystems and human food production. Effective, environmentally friendly, and inexpensive materials, such as biochar, are needed to reduce mobility and bioavailability of As and P. While biochar features several physicochemical properties that make it an ideal contaminant sorbent, certain modifications such as mineral-impregnation can improve sorption efficiencies for targeted compounds. Here, we conducted sorption experiments to investigate and quantify the potential utility of magnesium (Mg) for improving biochar sorption efficiency of P and As. We synthesized a Mg-modified walnut shells-derived biochar and characterized its ability to remove As and P from aqueous solutions, thereby mitigating losses of valuable P when needed while, at the same time, immobilizing hazardous As in ecosystems. SEM-EDX, FTIR and elemental analysis showed morphological and functional changes of biochar and the formation of new Mg-based composites (MgO, MgOHCl) responsible for improved sorption potential capacity by 10 times for As and 20 times for P. Sorption efficiency was attributed to improved AEC, higher SSA, chemical forms of sorbates and new sorption site formations. Synthetized Mg-composite/walnut shell-derived biochar also removed >90% of P from real samples of wastewater, indicating its potential suitability for contaminated waterbody remediation. [ABSTRACT FROM AUTHOR]

Harmful algal blooms have increased globally with warming of aquatic environments and increased eutrophication. Proliferation of cyanobacteria (blue-green algae) and the subsequent flux of toxic extracellular microcystins present threats to public and ecosystem health and challenges for remediation and management. Although methods exist, there is currently a need for more environmentally friendly and economically and technologically feasible sorbents. Biochar has been proposed in this regard because of its high porosity, chemical stability, and notable sorption efficiency for removing of cyanotoxins. In light of worsening cyanobacterial blooms and recent research advances, this review provides a timely assessment of microcystin removal strategies focusing on the most pertinent chemical and physical sorbent properties responsible for effective removal of various pollutants from wastewater, liquid wastes, and aqueous solutions. The pyrolysis process is then evaluated for the first time as a method for sorbent production for microcystin removal, considering the suitability and sorption efficiencies of pyrolysed materials and biochar. Inefficiencies and high costs of conventional methods can be avoided through the use of pyrolysis. The significant potential of biochar for microcystin removal is determined by feedstock type, pyrolysis conditions, and the physiochemical properties produced. This review informs future research and development of pyrolysed materials for the treatment of microcystin contaminated aquatic environments. [ABSTRACT FROM AUTHOR]