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Fluoride ion (F - ) is one of the major geogenic contaminants in water and soil. Excessive consumption of these geogenic contaminants poses serious health impacts on humans and plants. In this study, a novel carbonaceous material, nano-bonechar, was synthesized from cow bones and applied as a soil amendment at rates of 0, 0.5, 1, and 2% to remediate and revitalize naturally F - -contaminated soil. The results revealed that the nano-bonechar significantly reduced the mobility and bioavailability of F - by 90% in the contaminated soil, and improved the soil quality by increasing the soil water holding capacity, soil organic matter, and the bioavailable contents of PO 4 3- , Ca 2+ , and Na + . Subsequently, the pot experiment results showed a significant reduction in the uptake of F - by 93% in Zea mays plants. Moreover, the nano-bonechar application improved the plant's growth, as indicated by the higher fresh and dry weights, root and shoot lengths, and total content of PO 4 3- , Ca 2+ , and K + than those of un-amended soil. The F-immobilization in soil was mainly due to the presence of the hydroxyapatite [Ca 10 (PO 4 ) 6 (OH) 2 ] mineral in the nano-bonechar. Ion exchange between OH - (of nano-bonechar) and F - (of soil), and the formation of insoluble fluorite (CaF 2 ) contributed to the attenuation of F - mobility in the soil. It is concluded that nano-bonechar, due to its size and enrichment in hydroxyapatite, could successfully be utilized for the rapid remediation and revitalization of F - -contaminated agricultural soil., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Ltd. All rights reserved.)

The improper management of solid waste, particularly the dumping of untreated municipal solid waste, poses a growing global challenge in both developed and developing nations. The generation of leachate is one of the significant issues that arise from this practice, and it can have harmful impacts on both the environment and public health. This paper presents an overview of the primary waste types that generate landfill leachate and their characteristics. This includes examining the distribution of waste types in landfills globally and how they have changed over time, which can provide valuable insights into potential pollutants in a given area and their trends. With a lack of specific regulations and growing concerns regarding environmental and health impacts, the paper also focuses on emerging contaminants. Furthermore, the environmental and ecological impacts of leachate, along with associated health risks, are analyzed. The potential applications of landfill leachate, suggested interventions and future directions are also discussed in the manuscript. Finally, this work addresses future research directions in landfill leachate studies, with attention, for the first time to the potentialities that artificial intelligence can offer for landfill leachate management, studies, and applications., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 The Authors. Published by Elsevier B.V. All rights reserved.)

The objectives of this study were to determine selected Hofmeister anions and cations that are important for kidney health, in raw rice samples from selected Chronic Kidney Disease of unknown etiology (CKDu) endemic and non-endemic areas in Sri Lanka and their intake. The anions and cations were analyzed by Ion Chromatography and Microwave Plasma Atomic Emission Spectrometry (MP-AES), respectively, after alkaline and acid digestion in thirty raw rice samples each from CKDu endemic and non-endemic areas, and the dietary intake was estimated. The mean concentrations of fluoride (F - ), chloride (Cl - ), phosphate (PO 4 3- ), sulfate (SO 4 2- ), sodium (Na + ), magnesium (Mg 2+ ), potassium (K + ), and calcium (Ca 2+ ) in raw rice in CKDu endemic areas were 53.317, 1515.3, 2799.6, 2704.9, 30.603, 300.76, 1001.3, and 90.075 mg/kg, respectively. The mean concentration of the anions and cations in raw rice from CKDu non-endemic areas were 22.850, 947.52, 4418.7, 6080.2, 23.862, 364.45, 955.78, and 96.780 mg/kg, respectively. Significantly higher differences (p < 0.05) were reported in the mean concentration of F - , Cl - , and Na + in raw rice from CKDu endemic areas in comparison with the samples from non-endemic areas. The aggregated estimated daily intake (EDI) and cumulative EDI of F - via consumption of cooked non-traditional samba rice from CKDu endemic areas for adults were the highest (0.155 and 0.172 mg/kg bw/d, respectively), which were higher than the recommended tolerable upper intake value (0.15-0.2 mg/kg bw/d). In contrast, the traditional rice from CKDu non-endemic areas for adolescents, reported the lowest values (0.0210 and 0.0470 mg/kg bw/d, respectively). Adults who consume non-traditional samba rice from CKDu endemic areas were at health risk, while children were the most vulnerable group due to their low body weight. These results indicate that the consumption of rice rich in Hofmeister ions may contribute to the total intake and act as risk factors to negatively affect weak kidneys in CKDu endemic areas. Further research to analyze Hofmeister ions in cooked rice and rice from different countries is recommended., (© 2023. The Author(s), under exclusive licence to Springer Nature B.V.)

Hexavalent chromium (Cr(VI)) is deemed a priority contaminant owing to its carcinogenicity, teratogenicity, and mutagenicity towards flora and fauna. A novel Chitosan-modified Mimosa pigra biochar (CMPBC) was fabricated and the efficiency of Cr(VI) oxyanion removal in aqueous systems was compared with the pristine biochar. The instrumental characterization of X-ray photoelectron spectroscopy (XPS), and Fourier transform infrared spectroscopy (FT-IR) confirmed the amino modification of MPBC when treated with chitosan. Characteristic features of the Cr(VI) sorptive process by CMPBC and MPBC were examined by performing batch sorption studies. Experimental data suggested that sorption is heavily dependent on pH and the highest adsorption occurred at pH 3.0. The maximum adsorption capacity of CMPBC was 14.6 ± 1.07 mg g -1 . It was further noted that the removal efficiency of CMPBC (92%) was considerably greater than that of MPBC (75%) when the solution pH, biochar dose, and initial concentration of Cr(VI) are 3.0, 1.0 g L -1 and 5.0 mg L -1 respectively. The kinetic data were best interpreted by the power function model (R 2  = 0.97) suggesting a homogenous chemisorption process. The isotherm data for the removal of Cr(VI) by CMPBC was inferred well by Redlich Peterson (R 2 = 0.96) and Temkin (R 2 = 0.96) isotherms. Results of sorption-desorption regeneration cycles indicated that the Cr(VI) uptake by CMPBC is not fully reversible. The coexistence of Cr(VI) and Cr(III) on CMPBC was confirmed through the XPS analysis. The electrostatic attractions between cationic surface functionalities and Cr(VI) oxyanions, the partial reductive transformation of Cr(VI) species to Cr(III), as well as complexation of Cr(III) onto CMPBC were identified as the possible mechanisms of mitigation of Cr(VI) by CMPBC. The results and outcomes of this research suggest the possibility of utilizing the CMPBC as an easily available, environmentally sustainable, and inexpensive sorbent to decontaminate Cr(VI) from aqueous media., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier Inc. All rights reserved.)

The World Health Organization (WHO) recognised variant B.1.1.529 of the Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) as a variant of concern, termed "Omicron", on November 26, 2021. Its diffusion was attributed to its several mutations, which allow promoting its ability to diffuse worldwide and its capability in immune evasion. As a consequence, some additional serious threats to public health posed the risk to undermine the global efforts made in the last two years to control the pandemic. In the past, several works were devoted to discussing a possible contribution of air pollution to the SARS-CoV-2 spread. However, to the best of the authors' knowledge, there are still no works dealing with the Omicron variant diffusion mechanisms. This work represents a snapshot of what we know right now, in the frame of an analysis of the Omicron variant spread. The paper proposes the use of a single indicator, commercial trade data, to model the virus spread. It is proposed as a surrogate of the interactions occurring between humans (the virus transmission mechanism due to human-to-human contacts) and could be considered for other diseases. It allows also to explain the unexpected increase in infection cases in China, detected at beginning of 2023. The air quality data are also analyzed to evaluate for the first time the role of air particulate matter (PM) as a carrier of the Omicron variant diffusion. Due to emerging concerns associated with other viruses (such as smallpox-like virus diffusion in Europe and America), the proposed approach seems to be promising to model the virus spreading., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier Inc. All rights reserved.)

Most traditional oil spill clean-up techniques are still laboratory based and are expensive and fairly ineffective. This study investigated the capacity of biochars derived from bio-energy industries in oil spill remediation with a pilot-testing. Three different biochars from bio-energy industries, Embilipitya (EBC), Mahiyanganaya (MBC), and Cinnamon Wood Biochar (CWBC) were assessed for the removal of Heavy Fuel Oil (HFO) at three dosages (10, 25, and 50 g L -1 ). Pilot-scale experiment was conducted with 100 g of biochars separately in the oil slick of X-Press Pearl shipwreck. All adsorbents exhibited rapid oil removal (within 30 min). Isotherm data were well explained by Sips isotherm model (R 2  > 0.98). The pilot-scale experiment resulted oil removal for CWBC, EBC and MBC as 0.62, 1.12, and 0.67 g kg -1 respectively, even in rough sea conditions with a limited contact time (>5 min) indicates biochar's capacity in oil spill remediation as a cost-effective material., Competing Interests: Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: Meththika Vithanage reports financial support was provided by University of Sri Jayewardenepura. Meththika Vithanage reports administrative support and travel were provided by Marine Environment Protection Authority., (Copyright © 2023 Elsevier Ltd. All rights reserved.)

Removal of arsenic from drinking water is one of the most important global concerns. Among the various techniques, adsorptive removal of arsenic is considered as a viable most effective method. However, limited attention is given to understand the overall relative sorption capacity of different sorbents (e.g., biocomposite, biochar and nano-composite etc.) since various factors influence the sorption capacity. The aim of this study is to assess the effectiveness of various adsorbents with quantitative estimation (Langmuir adsorption maxima, Qmax) as well as to evaluate the influence of experimental conditions on the achievement of maximum adsorption. A number of analyses including meta-analysis, analysis of variance (ANOVA), scientometric and regression were performed. The results revealed that among the sorbents, nanoparticles show the greatest sorption capacity while pre-doped biochar performed the best among different biochars. Average across all sorbents, As (V) removal efficacy was higher than As (III). As expected, a high point of zero charge (PZC) and higher positive surface charge favored adsorption. The relative contribution of different mechanisms was also discussed. Our scientometric analyses revealed that, research should focus on the development of low-cost adsorbents and increase their reusability, safe disposal of adsorbed arsenic. Altogether, our findings provide a molecular understanding of arsenic sorption to different sorbents with implications for tailoring a good sorbent for arsenic removal from drinking water., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 Elsevier B.V. All rights reserved.)

Dietary exposure of selected Hofmeister ions-fluoride, chloride, sulfate, phosphate, sodium, potassium, magnesium, and calcium from black tea consumption in chronic kidney disease of unknown etiology (CKDu) prevalent areas in Sri Lanka-were assessed in order to understand exposure and risk. Black tea samples (n = 25) were collected from CKDu prevalent areas and control areas (n = 15). Total fluoride content in alkali fused digested black tea samples was determined. The available Hofmeister ions in tea infusions prepared using deionized water and the groundwater collected by CKDu endemic areas were compared. Dietary exposure was calculated by chronic daily intake data. Total fluoride concentrations ranged from 80 to 269 mg/kg in tea collected from the CKDu endemic regions and 62.5-123.5 mg/kg in non-endemic regions. The fluoride content in infusions ranged from 1.45 to 2.04 mg/L in CKDu endemic areas and 1.11-1.38 mg/L in control samples. The infusions prepared with local groundwater from the CKDu endemic areas showed an elevated level of fluoride 95% than that of the infusion prepared using same tea with deionized water. Aggregated chronic daily intake value from tea and groundwater exceeds the estimated adequate daily intake value of fluoride. The hazard quotient (HQ) values of fluoride in 5 min and 120 min tea infusions were 1.60 and 2.20, respectively, and indicate an adverse health risk. Potassium content in tea infusions collected from CKDu endemic areas is higher than in the control. Even though these values are less than the adequate intake, it may pose an impairment on a weak kidney. Chronic daily intake of Hofmeister ions, i.e., fluoride and potassium from black tea consumed in CKDu endemic areas may induce a risk for CKDu., (© 2023. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)

Exposure to excess fluoride is a controversial public health concern as it can cause dental/skeletal fluorosis as well as renal toxicity. The study intended to evaluate the synergistic interaction of clay intercalation and thermochemical modification on corncob biochar to remove fluoride from aqueous solutions. Layered double hydroxide was assorted with thermally activated (torrefaction and pyrolysis) corncob biochar at 1:1 (w/w) ratio to obtain composites called LDH-CCBC250 and LDH-CCBC500. Physicochemically characterized adsorbents were assessed against the pH (3-9), reaction time (up to 12 h) and initial fluoride concentration (0.5-10 mg L -1 ) for defluoridation. The porous structure of biochar was found to be richer compared to biocharcoal. The adsorption performance of LDH-CCBC500 was 6-fold higher compared to LDH-CCBC250 signifying the pronounced effect of thermal activation. Fluoride adsorption was pH dependent, and the best pH was in the range of pH 3.5-5.0 and there was no ionic strength dependency. Fluoride uptake by LDH-CCBC500 follows pseudo-second order and Elovich kinetic models, which suggests a chemisorption process followed by physisorption. The most expected way to eliminate fluoride by LDH-CCBC500, which had a maximum adsorption capacity of 7.24 mg g -1 , was cooperative chemical adsorption upon the Langmuir and Hills isotherm (r 2  = 0.99) parameters. Layered double hydroxide intercalated corncob biochar derived from slow pyrolysis is best performing in acidic waters., Competing Interests: Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests:Meththika Vithanage reports financial support was provided by National Science Foundation, Sri Lanka., (Copyright © 2023 Elsevier Ltd. All rights reserved.)

Microplastics has become a global concern due to their ubiquitous presence which poses unavoidable human exposure risks. Geographical distribution and yearly trends of research on microplastics, food, and beverages do not exist. Thus, no overall account is available regarding the presence of microplastics and plastics-associated contaminants in food and beverages. Hence, this attempt is to review the geographical distribution of studies through a brief bibliometric analysis and the plastics-associated contaminants including plasticizers and microplastics in food and beverages. Estimated microplastic consumption has been listed for the pool of publications reviewed here. Further, this review discusses the ingestion potency of micropollutants associated with microplastics, possible health impacts, and existing challenges. Global trend in research exponentially increased after 2018 and China is leading. Studies on microplastics were limited to a few beverages and food; milk, beer, tea, refreshing drinks, salt, sugar, honey, etc., whereas seafood and drinking water have been extensively studied. Publications on plastic-additives were reported in two ways; migration of plastic-additives from packaging by leaching and the presence of plastic-additives in food and beverages. Bisphenol A and bis(2-Ethylhexyl) phthalate were the most frequently reported both in food and beverages. Exposure of packaging material to high temperatures predominantly involves plastic-additive contamination in food and beverages. Microplastics-bound micropollutants can also be ingested through food and beverages; however, a lack of knowledge exists. The complex matrix of food or beverages and the absence of standard procedures for analysis of microplastics and micropollutants exist as challenges. More investigations on the presence of microplastics and plastic-additives in food and beverage are urgent needs to a better assessment of potential human exposure and human health risk., Competing Interests: Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests:, (Copyright © 2022 Elsevier Ltd. All rights reserved.)

The emergence of novel respiratory disease (COVID-19) caused by SARS-CoV-2 has become a public health emergency worldwide and perturbed the global economy and ecosystem services. Many studies have reported the presence of SARS-CoV-2 in different environmental compartments, its transmission via environmental routes, and potential environmental challenges posed by the COVID-19 pandemic. None of these studies have comprehensively reviewed the bidirectional relationship between the COVID-19 pandemic and the environment. For the first time, we explored the relationship between the environment and the SARS-CoV-2 virus/COVID-19 and how they affect each other. Supporting evidence presented here clearly demonstrates the presence of SARS-CoV-2 in soil and water, denoting the role of the environment in the COVID-19 transmission process. However, most studies fail to determine if the viral genomes they have discovered are infectious, which could be affected by the environmental factors in which they are found.The potential environmental impact of the pandemic, including water pollution, chemical contamination, increased generation of non-biodegradable waste, and single-use plastics have received the most attention. For the most part, efficient measures have been used to address the current environmental challenges from COVID-19, including using environmentally friendly disinfection technologies and employing measures to reduce the production of plastic wastes, such as the reuse and recycling of plastics. Developing sustainable solutions to counter the environmental challenges posed by the COVID-19 pandemic should be included in national preparedness strategies. In conclusion, combating the pandemic and accomplishing public health goals should be balanced with environmentally sustainable measures, as the two are closely intertwined., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 Elsevier Inc. All rights reserved.)

Hydroxyapatite (HAP) is an easily synthesizable, low-cost mineral that has been recognized as a potential material for fluoride removal. Some of the synthesis methods of HAP are quite straightforward and cost-effective, while some require sophisticated synthesis techniques under advanced laboratory conditions. This review assesses the physicochemical characteristics of HAP and HAP-based composites produced via various techniques, their recent development in defluoridation and most importantly, the fluoride removal performances. For the first time, fluoride removal performances of HAP and HAP composites are compared based on partition coefficient (K D ) instead of maximum adsorption capacity (Q max ), which is significantly influenced by initial loading concentrations. Novel HAP tailored composites exhibit comparatively high K D values indicating the excellent capability of fluoride removal along with specific surface areas above 120 m 2 /g. HAP doped with aluminium complexes, HAP doped ceramic beads, HAP-pectin nanocomposite and HAP-stilbite nanocomposite, HAP decorated nanotubes, nanowires and nanosheets demonstrated high Q max and K D . The secret of HAP is not the excellent fluoride removal performances but best removal at neutral and near-neutral pH, which most of the defluoridation materials are incapable of, making them ideal adsorbents for drinking water treatment. Multiple mechanisms including physical surface adsorption, ion-exchange, and electrostatic interactions are the main mechanisms involved in defluoridation. Further research work must be focused on upscaling HAP-based composites for defluoridation on a commercial scale., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 Elsevier Ltd. All rights reserved.)

Extensive use of per- and polyfluoroalkyl substances (PFASs) in various industrial activities and daily-life products has made them ubiquitous contaminants in soil and water. PFAS-contaminated soil acts as a long-term source of pollution to the adjacent surface water bodies, groundwater, soil microorganisms, and soil invertebrates. While several remediation strategies exist to eliminate PFASs from the soil, strong ionic interactions between charged groups on PFAS with soil constituents rendered these PFAS remediation technologies ineffective. Pilot and field-scale data from recent studies have shown a great potential of PFAS to bio-accumulate and distribute within plant compartments suggesting that phytoremediation could be a potential remediation technology to clean up PFAS contaminated soils. Even though several studies have been performed on the uptake and translocation of PFAS by different plant species, most of these studies are limited to agricultural crops and fruit species. In this review, the role of both aquatic and terrestrial plants in the phytoremediation of PFAS was discussed highlighting different mechanisms underlying the uptake of PFASs in the soil-plant and water-plant systems. This review further summarized a wide range of factors that influence the bioaccumulation and translocation of PFASs within plant compartments including both structural properties of PFASs and physiological properties of plant species. Even though phytoremediation appears to be a promising remediation technique, some limitations that reduced the feasibility of phytoremediation in the practical application have been emphasized in previous studies. Additional research directions are suggested, including advanced genetic engineering techniques and endophyte-assisted phytoremediation to upgrade the phytoremediation potential of plants for the successful removal of PFASs., (Copyright © 2022 Elsevier Inc. All rights reserved.)

The objectives of the study were to evaluate and compare the efficacy of hexavalent chromium (Cr(VI)) removal by amino-modified (HDA-MPBC) and pristine biochar (MPBC) derived from an invasive plant Mimosa pigra. Prepared biochars were characterized and batch experiments were conducted to check the performance and the mechanisms of Cr(VI) removal. FTIR spectra revealed that the surface of HDA-MPBC is abundant with amino functional groups which was further confirmed by XPS analysis. The highest Cr(VI) removal for both HDA-MPBC (76%) and MPBC (62%) was observed at pH 3.0. The batch sorption data were well fitted to the Freundlich isotherm model and pseudo-second-order kinetic model, suggesting the involvement of both physisorption and chemisorption mechanisms for Cr(VI) removal. X-ray photoelectron spectroscopy studies showed that both Cr(VI) and Cr(III) were presented at the modified biochar surface after adsorption. These results indicated that the electrostatic attraction of Cr(VI) coupled with reduction of Cr(VI) to Cr(III) and complexation of Cr(III) ions with functional groups on HDA-MPBC as the most plausible mechanism for removal of Cr(VI) by modified biochar. Regeneration experiment concluded that adsorbed Cr(VI) onto the surface of HDA-MPBC had the least tendency of being desorbed in basic conditions. HDA-MPBC showed a high performance in adsorptive removal of Cr(VI) compared to pristine biochar signifying the amino modification to enhance adsorption performance of biochar in Cr(VI) removal from wastewater., (Copyright © 2022 Elsevier Inc. All rights reserved.)

Menstrual hygiene waste management has received lack of attention and hence it has been poorly investigated, mainly due to its association to social and cultural aspects of a natural process, that is often surrounded of entrenched stigma and taboos. Therefore, data about quantities and full lifecycle of the generated waste are often not available or suffer of large incertitude. However, this argument represents a relevant and critical issue, not only for the health of the women, their equality, and dignity, but also possible associated environmental concerns. This work highlights the necessity and the urgency to face the problems associated with menstrual hygiene waste, which cannot be still considered only relegated to low-income countries. It gives the dimension of the waste associated to migrants in the incoming areas, which is often neglected in sanitation program implementation. This work also describes the existing knowledge gaps and suggests some actions to implement in the next future. In the pandemic context, menstrual hygiene needs urgent attention, also to understand the possible implication of this waste, generated for example in refugees' camps, in SARS-CoV-2 spread, and to prevent eventual unknown environmental issues connected with the reconvention of some factories from the production of menstrual hygiene products to facemasks manufacture., Competing Interests: The authors declare no conflict of interest., (© 2022 The Author(s).)

Objectives of the present research were to examine the capacity of disc-milled high lignin biochar colloids (CBC) for the removal of ciprofloxacin (CPX) from aqueous solution and synthetic hydrolyzed human urine. In this study, adsorption of CPX was tested against the initial pH (3-10), ionic strength (0.001-0.1 M NaNO 3 ), resident time (up to 8 h), initial CPX concentration (5-100 mg/L) and temperature (25, 35, and 45 °C). The surface morphology was examined using Brunauer-Emmett-Teller (BET) specific surface area. The CBC was observed to be < 300 nm whereas the BET surface area was 284 m 2 /g. Best CPX adsorption demonstrated at pH 5-6 and however, indicated ionic strength dependency. Experimental kinetics data in aqueous media were well-fitted to the pseudo-second-order (r 2 of 0.98), while the Hill and Langmuir isotherm models best described the isotherm data (r 2 of 0.95 and 0.94, respectively) confirming chemisorption followed by physisorption interactions. The thermodynamics results indicate that CPX adsorption onto CBC is spontaneous (-ΔG), endothermic (+ΔH) and has increased randomness (+ΔS) in the aqueous system. The kinetic experimental data in synthetic urine matrix was fitted with Elovich (r 2  = 0.99) and fractional power (r 2  = 0.96) models whereas Hills (r 2  = 0.99) and Langmuir (r 2  = 0.97) models were the most fitted with isotherm data suggesting the adsorption of CPX on the CBC by chemisorption mechanisms. In conclusion, CBC demonstrated effective removal of CPX indicating its potential to be used in wastewater treatment., (Copyright © 2022 Elsevier Ltd. All rights reserved.)

The contamination of natural resources by hexavalent chromium (Cr(VI)) originating from natural and anthropogenic activities is a serious environmental concern. Although many articles on chromium remediation have been published, a comprehensive understanding of the mechanisms involved in remediation with different sorbents is not yet available. In this systematic review, the performance and applicability of several adsorptive materials for Cr(VI) removal from aqueous media are discussed, along with a detailed analysis of the mechanisms involved. Statistical analysis is applied to compare the efficacies of different adsorbents, while a similar approach is used to determine the effects of sorbent properties and experimental conditions on the adsorption capacity. A detailed analysis of the factors involved in fixed-bed column studies is also presented. A suitable desorption approach to the regeneration of the spent adsorbent and its adsorption performance in reuse is also examined. Among the different sorbents, nanoparticles and mineral-doped biochar were found to be the most effective sorbents, while the adsorption was higher at low pH (~4.0) than that at intermediate pH (6-8). Contrary to our expectation, adsorption was high for sorbents with low specific surface areas, suggesting that the adsorption of Cr(VI) is largely influenced by the chemical properties of the sorbents. The optimum adsorption in fixed-bed column systems is obtained at a lower Cr(VI) ion concentration, a lower influent flow rate, and a higher bed height. Since most of the studies reviewed herein were merely experimental and utilized ideal conditions with the presence of a single contaminant, i.e. Cr(VI) in water, further studies on adsorption dynamics with the presence of other interfering ions are suggested. This review is promising for the further development of Cr(VI) removal strategies and closes the research gaps pertaining to their challenges., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2021 Elsevier B.V. All rights reserved.)

The production of biochar from sewage sludge pyrolysis is a promising approach to transform the waste resultant from wastewater treatment plants (WWTPs) to a potential adsorbent. The current review provides an up-to-date review regarding important aspects of sewage sludge pyrolysis, highlighting the process that results major solid fraction (biochar), as high-value product. Further, the physio-chemical characteristics of sewage-sludge derived biochar such as the elemental composition, specific surface area, pore size and volume, the functional groups, surface morphology and heavy metal content are discussed. Recent progress on adsorption of metals, emerging pollutants, dyes, nutrients and oil are discussed and the results are examined. The sewage sludge-derived biochar is a promising material that can make significant contributions on pollutants removal from water by adsorption and additional benefit of the management of huge volume of sewage. Considering all these aspects, this field of research still needs more attention from the researchers in the direction of the technological features and sustainability aspects., (Copyright © 2021 Elsevier Ltd. All rights reserved.)

The prevalence of chronic kidney disease of unknown etiology (CKDu) is receiving considerable attention due to the serious threat to human health throughout the world. However, the roles of geo-socio-environmental factors in the prevalence of the CKDu endemic areas are still unknown. Sri Lanka is one of the countries most seriously affected by CKDu, where 10 out of 25 districts have been identified as the areas with the high prevalence of CKDu (10-20%). This review summarizes the geographical distribution of CKDu and its probable geochemical, behavioral, sociological, and environmental risk factors based on research related to hydrogeochemical influences on CKDu in Sri Lanka. More than 98% of CKDu patients have consumed groundwater as their primary water source in daily life, indicating the interactions of geogenic contaminants (such as F - , total dissolved solids, Hofmeister ions) in groundwater is responsible for the disease. Apart from the hydrogeochemical factors, mycotoxins, cyanotoxins, use of some herbal medicines, dehydration, and exposure to agrochemicals were alleged as risk factors. Sociological factors, including poverty, living habits and anthropogenic activities, may also provoke the emergence of CKDu. Therefore, the interaction of geo-socio environmental risk factors should be sociologically and scientifically considered to prevent the prevalence of CKDu. Future in-depth studies are required to reveal the individual role of each of the postulated etiological factors, possibly using machine learning and advanced statistics., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2021 Elsevier B.V. All rights reserved.)

Recently, the adsorption-based environmental remediation techniques have gained a considerable attention, due to their economic viability and simplicity over other methods. Hence, detailed presentation and analysis were herein focused on describing the role of biochar in oil spill removal. Oil removal by utilizing biochar is assumed as a green-oriented concept. Biochar is a carbon-rich low-cost material with high porosity and specific surface chemistry, with a tremendous potentiality for oil removal from aqueous solutions. Oil sorption properties of biochar mainly depend on the biochar production/synthesis method, and the biomass feedstock type. In order to preserve the stability of functional groups in the structure, biochar needs to be produced/activated at low temperatures (<700 ᵒC). In general, biochar derived from biomass containing high lignin content via slow pyrolysis is more favorable for oil removal. Exceptional characteristics of biochar which intensify the oil removal capability such as hydrophobicity, oleophilicity or/and specific contaminant-surface interaction of biochar can be enhanced and be tuned by chemical and physical activation methods. Considering all the presented results, future perspectives such as the examination of biochar efficacy on oil removal efficiency in multi-element contaminated aqueous solutions to identify the best biomass feedstocks, the production protocols and large-scale field trials, are also discussed., (Copyright © 2021 Elsevier Ltd. All rights reserved.)

Water scarcity and its pollution has become a concern in recent times. The disposal of nutrient-rich (nitrogen and phosphorous) wastewater is also one of the main cause of water pollution through eutrophication, reduced dissolved oxygen that poses threat to aquatic ecosystems. As a result, nutrient removal has become a mandate apart from the removal of organics. However, the removal of nutrients from sewage is a challenging task. Conversely, conventional biological treatment processes provide little relief in nutrient removal. The treated effluents from conventional biological processes do not achieve the stringent nutrient removal disposal standard limits and become primary cause of pollution in the receiving water bodies. This has stressed upon the need for eco-friendly, low-energy and cost-efficient nutrient removal treatment technologies. Various biological treatment combinations or variants are in use for the efficient removal of nutrients. The biological processes in itself or in combination with chemical processes are preferred over technologies based solely on physico-chemical processes for its treatment performance at lower cost. This review summarizes the existing treatment processes and their possible up-gradation with the aim to accomplish the marked effluent standards for the nutrients. The concept of conventional systems and advanced systems for nutrients (nitrogen and phosphorous) removal which are already developed or under development are deeply discussed. Further, the challenges of each treatment systems are abridged. Finally, the possible suggestions for the modification/retrofitting of existing treatment systems for achieving stringent disposal standards are pointed out., (Copyright © 2021 Elsevier Ltd. All rights reserved.)

This review focuses on existing technologies for carcass and corpse disposal and potential alternative treatment strategies. Furthermore, key issues related to these treatments (e.g., carcass and corpse disposal events, available methods, performances, and limitations) are addressed in conjunction with associated environmental impacts. Simultaneously, various treatment technologies have been evaluated to provide insights into the adsorptive removal of specific pollutants derived from carcass disposal and management. In this regard, it has been proposed that a low-cost pollutant sorbent may be utilized, namely, biochar. Biochar has demonstrated the ability to remove (in)organic pollutants and excess nutrients from soils and waters; thus, we identify possible biochar uses for soil and water remediation at carcass and corpse disposal sites. To date, however, little emphasis has been placed on potential biochar use to manage such disposal sites. We highlight the need for strategic efforts to accurately assess biochar effectiveness when applied towards the remediation of complex pollutants produced and circulated within carcass and corpse burial systems., Competing Interests: Competing interestsThe authors declare that they have no competing interests., (© The Author(s) 2021.)

In this paper, we investigate the release of heavy metals from sludge produced from an electrical industry using both organic and inorganic acids. Single and sequential extractions were conducted to assess heavy metals in different phases of the sludge. Metal release from sludge was investigated in the presence of three inorganic acids (nitric, sulfuric, and phosphoric) and three organic acids (acetic, malic, and citric) at concentrations ranging from 0.1 to 2.0 mol L -1 . Sequential extraction indicated the presence of Cu primarily in the carbonate fraction, Pb in the residual fraction, and Ni in the FeMn oxide fraction. The cumulative release rates of heavy metals (i.e., Pb, Cu, and Ni) by 1.0 mol L -1 of acid increased with the use of the following acids in the order of: malic < sulfuric < acetic < phosphoric < citric < nitric. Acetic acid exhibited the highest release of Cu, at a rate of 72.62 × 10 -11  mol m -2  s -1 at pH 1, and malic acid drove the release of Pb at a maximum rate of 3.90 × 10 -11  mol m -2  s -1 . Meanwhile, nitric acid provided the maximum rate of Ni release (0.23 × 10 -11  mol m -2  s -1 ) at pH 1. The high rate of metal release by organic acids is explained through ligand-promoted mechanisms that enhance the release of metal ions from the sludge. The results from our study emphasize that an understanding of the metal release mechanism is key to selecting the optimal acid for the maximum recovery of heavy metals., (Copyright © 2019. Published by Elsevier B.V.)

This study evaluates a novel adsorbent for ciprofloxacin (CPX) removal from water using a composite derived from municipal solid waste biochar (MSW-BC) and montmorillonite (MMT). The composite adsorbent and pristine materials were characterized using powder X-Ray Diffraction (PXRD), Fourier-Transform Infrared (FTIR) spectroscopy, and Scanning Electron Microscope (SEM) before and after the adsorption. Batch experiments were conducted to study the mechanisms involved in the adsorption process. Ciprofloxacin sorption mechanisms were interpreted in terms of its pH-dependency and the distribution coefficients. The SEM images confirmed the successful binding of MMT onto the MSW-BC through flaky structure along with a porous morphology. Encapsulation of MMT onto MSW-BC was exhibited through changes in the basal spacing of MMT via PXRD analysis. Results from FTIR spectra indicated the presence of functional groups for both pristine materials and the composite that were involved in the adsorption reaction. The Hill isotherm model and pseudo-second-order and Elovich kinetic models fitted the batch sorption data, which explained the surface heterogeneity of the composite and cooperative adsorption mechanisms. Changes made to the MSW-BC through the introduction of MMT, enhanced the active sites on the composite adsorbent, thereby improving its interaction with ionizable CPX molecules giving high sorption efficiency., (Copyright © 2019 Elsevier Ltd. All rights reserved.)

The focus of this research was to synthesize novel clay-biochar composites by incorporating montmorillonite (MMT) and red earth (RE) clay materials in a municipal solid waste (MSW) biochar for the adsorptive removal of tetracycline (TC) from aqueous media. X-ray Fluorescence Analysis (XRF), Fourier Transform Infrared Spectroscopy (FTIR), Powder X-ray Diffraction (PXRD) and Scanning Electron Microscopy (SEM) were used for the characterization of the synthesized raw biochar (MSW-BC) and clay-biochar composites (MSW-MMT and MSW-RE). Results showed that minute clay particles were dispersed on biochar surfaces. The FTIR bands due to Si-O functional group vibrations in the spectra of the clay-biochar composites provided further evidence for successful composite formation. The kinetic TC adsorption data of MSW-MMT were well fitted to the Elovich model expressing high surface activity of biochar and involvement of multiple mechanisms in the adsorption. The kinetic TC adsorption data of MSW-BC and MSW-RE were fitted to the pseudo second order model indicating dominant contribution of chemisorption mechanism during the adsorption. The adsorption differentiation obtained in the kinetic studies was mainly due to the structure of the combined clay material. The adsorption isotherm data of all the adsorbents were well fitted to the Freundlich model suggesting that the adsorption of TC onto the materials occurred via both physisorption and chemisorption mechanisms. In comparison to the raw biochar and MSW-RE, MSW-MMT exhibited higher TC adsorption capacity. Therefore, MSW-MMT clay-biochar composite could be applied in the remediation of TC antibiotic residues in contaminated aqueous media., (Copyright © 2019 Elsevier Ltd. All rights reserved.)

This study investigates the adsorption of ciprofloxacin (CPX) onto a municipal solid waste derived biochar (MSW-BC) and a composite material developed by combining the biochar with bentonite clay. A bentonite-MSW slurry was first prepared at 1:5 ratio (w/w), and then pyrolyzed at 450 °C for 30 min. The composite was characterized by scanning electron microscopy (SEM), Powder X-ray diffraction (PXRD) and Fourier transform infrared (FTIR) spectroscopy before and after CPX adsorption. Batch experiments were conducted to assess the effect of pH, reaction time and adsorbate dosage. The SEM images confirmed successful modification of the biochar with bentonite showing plate like structures. The PXRD patterns showed changes in the crystalline lattice of both MSW-BC and the composite before and after CPX adsorption whereas the FTIR spectra indicated merging and widening of specific bands after CPX adsorption. The optimum CPX adsorption was achieved at pH 6, and the maximum adsorption capacity of the composite calculated via isotherm modeling was 190 mg/g, which was about 40% higher than the pristine MSW-BC. The Hill isotherm model along with pseudo-second order and Elovich kinetic models showed the best fit to the adsorption data. The most plausible mechanism for increased adsorption capacity is the increased active sites of the composites for CPX adsorption through induced electrostatic interactions between the functional groups of the composite and CPX molecules. The added reactive surfaces in the composite because of bentonite incorporation, and the intercalation of CPX in the clay interlayers improved the adsorption of CPX by the biochar-bentonite composite compared to the pristine biochar. Thus, MSW-BC-bentonite composites could be considered as a potential material for remediating pharmaceuticals in aqueous media., (Copyright © 2019 Elsevier Ltd. All rights reserved.)

Fluorescence excitation-emission matrix (EEM) spectroscopy coupled with parallel factor analysis (PARAFAC) enables better understanding of the nature of dissolved organic matter (DOM). In the current study, we characterized 10 biochar samples produced from different feedstocks using EEM/PARAFAC analysis. The composition and distribution of DOM substances present in biochar varied significantly according to feedstock, activation, and pyrolysis temperature. The integration of proximate and ultimate analyses of the solid phase together with water extractable organic matter (WEOM) phase of biochar provided new insights into the characterization of biochars, including nature and functionality. Characterization of both WEOM and solid phases is recommended for biochar research before large-scale production for various environmental and industrial applications., (Copyright © 2018 Elsevier Ltd. All rights reserved.)

Ammonium (NH 4 + ) is a common form of reactive nitrogen in wastewater, and its discharge to water bodies can lead to eutrophication. This study was conducted to understand NH 4 + adsorption mechanisms of pine sawdust and wheat straw biochars in aqueous solutions and the factors affecting NH 4 + removal. Biochars were produced by pyrolysing pine sawdust at 300 °C (PS300) and 550 °C (PS550) and wheat straw at 550 °C (WS550). Pseudo-second-order and Redlich-Peterson models best fitted the adsorption data. The PS300 showed the highest NH 4 + adsorption capacity (5.38 mg g -1 ), followed by PS550 (3.37 mg g -1 ) and WS550 (2.08 mg g -1 ). Higher H/C and O/C ratios of PS300 (0.78 and 0.32, respectively) indicated the greater presence of functional groups on the biochar's surface as compared to PS550 (0.35 and 0.10, respectively) and WS550 (0.36 and 0.08, respectively), resulting in different NH 4 + adsorption through electrostatic interactions. The dominant mechanism for NH 4 + adsorption by the biochars was likely chemical bonding and electrostatic interaction of NH 4 + with the surface functional groups. Lower pyrolysis temperature resulted in a higher NH 4 + adsorption capacity by the pine sawdust biochar. At the same pyrolysis temperature (550 °C), the biochar made with pine sawdust as the feedstock had a higher NH 4 + adsorption capacity than biochar made from wheat straw. We conclude that biochars can be efficient absorbents for NH 4 + removal from wastewater, and the removal efficiency can be optimised by selecting different feedstocks or the pyrolysis condition for biochar production.

Biochar is recognized as an effective material for recovering excess nutrients, including phosphorus (P), from aqueous solutions. Practically, that benefits the environment through reducing P losses from biochar-amended soils; however, how salinity influences P sorption by biochar is poorly understood and there has been no direct comparison on P sorption capacity between biochars derived from different feedstock types under non-saline and saline conditions. In this study, biochars derived from wheat straw, hardwood, and willow wood were used to compare P sorption at three levels of electrical conductivity (EC) (0, 4, and 8 dS m -1 ) to represent a wide range of salinity conditions. Phosphorus sorption by wheat straw and hardwood biochars increased as aqueous solution P concentration increased, with willow wood biochar exhibiting an opposite trend for P sorption. However, the pattern for P sorption became the same as the other biochars after the willow wood biochar was de-ashed with 1 M HCl and 0.05 M HF. Willow wood biochar had the highest P sorption (1.93 mg g -1 ) followed by hardwood (1.20 mg g -1 ) and wheat straw biochars (1.06 mg g -1 ) in a 25 mg L -1 P solution. Although the pH in the equilibrium solution was higher with willow wood biochar (~ 9.5) than with the other two biochars (~ 6.5), solution pH had no or minor effects on P sorption by willow wood biochar. The high sorption rate of P by willow wood biochar could be attributed to the higher concentrations of salt and other elements (i.e., Ca and Mg) in the biochar in comparison to that in wheat straw and hardwood biochars; the EC values were 2.27, 0.53, and 0.27 dS m -1 for willow wood, wheat straw, and hardwood biochars, respectively. A portion of P desorbed from the willow wood biochar; and that desorption increased with the decreasing P concentration in the aqueous solution. Salinity in the aqueous solution influenced P sorption by hardwood and willow wood but not by wheat straw biochar. We conclude that the P sorption capacity of the studied biochars is dependent on the concentration of the soluble element in the biochar, which is dependent on the biochar type, as well as the salinity level in the aqueous solution.

Biochar is an emerging low-cost sorbent used for removing trace metals from water. In this study, we evaluated the removal potential of aqueous hexavalent chromium (Cr(VI)) by biochars produced from soybean (Glycinemax L.) and burcucumber (Sicyos angulatus L.) residues. The highest Cr(VI) removal from solution occurred at low pH values (pH2-5), and adsorption decreased approximately tenfold when the pH increased from 2 to 10. Synchrotron-based X-ray absorption spectroscopy (XAS) investigations showed that Cr(VI) species were reduced to trivalent chromium (Cr(III)) at the biochar surface following Cr(VI) adsorption. Linear combination fitting (LCF) of X-ray absorption near edge structure (XANES) data indicated that approximately 90% of the total Cr(VI) (962μM) was reduced to Cr(III). Extended X-ray absorption fine structure (EXAFS) fitting results yielded interatomic chromium (CrCr) distances consistent with the formation of Cr(III) precipitates as Cr(OH) 3 . Trivalent chromium is far less soluble than Cr(VI) and typically precipitates as amorphous Cr(III) solids. Thus, biochars produced by soybean and burcucumber residues are a promising technique for both adsorbing and reductively immobilizing Cr(VI) from aqueous solutions., (Copyright © 2017 Elsevier B.V. All rights reserved.)

Unfortunately, in the original publication of the article, Prof. Yong Sik Ok's affiliation was incorrectly published. The author's affiliation is as follows.

This study examined the effects of carbon nanotube and biochar on the bioavailability of Pb, Cu and Sb in the shooting range soils for developing low-cost remediation technology. Commercially available multi-walled carbon nanotube (MWCNT) and biochar pyrolyzed from soybean stover at 300 °C (BC) at 0.5, 1 and 2.5% (w w -1 ) were used to remediate the contaminated soil in an incubation experiment. Both DTPA (bioavailable) and TCLP (leaching) extraction procedures were used to compare the metal/loid availability and leaching by the amendments in soil. The addition of BC was more effective in immobilizing mobile Pb and Cu in the soil than that in MWCNT. The BC reduced the concentrations of Pb and Cu in the soil by 17.6 and 16.2%, respectively. However, both MWCNTs and BC increased Sb bioavailability by 1.4-fold and 1.6-fold, respectively, in DTPA extraction, compared to the control. The toxicity characteristic leaching procedure (TCLP) test showed that the leachability of Pb in the soil amended with 2.5% MWCNT was 1.3-fold higher than that the unamended soil, whereas the BC at 2.5% decreased the TCLP-extractable Pb by 19.2%. Precipitation and adsorption via electrostatic and π-π electron donor-acceptor interactions were postulated to be involved in the interactions of Pb and Cu with surfaces of the BC in the amended soils, whereas ion exchange mechanisms might be involved in the immobilization of Cu in the MWCNT-amended soils. The application of BC derived from soybean stover can be a low-cost technology for simultaneously immobilizing bioavailable Pb and Cu in the shooting range soils; however, neither of amendments was effective in Sb immobilization.

This study assesses the distribution of goiter in the Kalutara District, Sri Lanka in order to find causative factors for the occurrence of goiter even after the salt iodization. A questionnaire survey was conducted at the household level and at the same time iodine and selenium levels of the water sources were analyzed. Questionnaire survey results indicated the highest numbers of goiter patients in the northern part where the lowest were found in the southern sector which may be due to the presence of acid sulfate soils. Females were more susceptible and it even showed a transmittance between generations. Average iodine concentrations in subsurface water of goiter endemic regions are 28.25 ± 15.47 μg/L whereas non-goiter regions show identical values at 24.74 ± 18.29 μg/L. Surface water exhibited relatively high values at 30.87 ± 16.13 μg/L. Endemic goiter was reported in some isolated patches where iodine and selenium concentrations low, latter was <10 μg/L. The formation of acid sulfate soils in the marshy lands in Kalutara district may lead to transformation of biological available iodine oxidation into volatile iodine by humic substances, at the same time organic matter rich peaty soil may have strong held of iodine and selenium which again induced by low pH and high temperature were suggested as the instrumental factors in the endemic goiter in Kalutara district. Hence, geochemical features such as soil pH, organic matter and thick lateritic cap in the Kalutara goiter endemic area play a role in controlling the available selenium and iodine for food chain through plant uptake and in water.

The use of biochar has been suggested as a means of remediating contaminated soil and water. The practical applications of conventional biochar for contaminant immobilization and removal however need further improvements. Hence, recent attention has focused on modification of biochar with novel structures and surface properties in order to improve its remediation efficacy and environmental benefits. Engineered/designer biochars are commonly used terms to indicate application-oriented, outcome-based biochar modification or synthesis. In recent years, biochar modifications involving various methods such as, acid treatment, base treatment, amination, surfactant modification, impregnation of mineral sorbents, steam activation and magnetic modification have been widely studied. This review summarizes and evaluates biochar modification methods, corresponding mechanisms, and their benefits for contaminant management in soil and water. Applicability and performance of modification methods depend on the type of contaminants (i.e., inorganic/organic, anionic/cationic, hydrophilic/hydrophobic, polar/non-polar), environmental conditions, remediation goals, and land use purpose. In general, modification to produce engineered/designer biochar is likely to enhance the sorption capacity of biochar and its potential applications for environmental remediation., (Copyright © 2016 Elsevier Ltd. All rights reserved.)

Biochar (BC) could be a potential candidate for the remediation of metal contaminated soil. Mechanistic understandings are needed for the appropriate selection of BC and investigating molecular microbial ecological interactions. The soybean stover-derived BCs were more effective in immobilizing Pb (88%) and Cu (87%) than the pine needle-derived BCs in a contaminated shooting range soil. The sequential chemical extractions indicated that BCs stimulated the geochemical transformation of metal species. Spectroscopic investigations using scanning electron microscopic elemental dot mapping and extended X-ray absorption fine structure spectroscopic measurements showed that Pb in the BCs amended soils was immobilized by the formation of stable chloropyromorphite. Soil organic C and microbial activity were also enhanced by BC. The non-labile C fraction in the soil amended with BCs produced at 700°C was increased. Biochars showed less impact on the bacterial community than feedstock biomass as promulgated by the pyrosequencing of 16S rRNA gene. The feedstock type (namely soybean stover and pine needles) was the main factor influencing the BCs efficacy on metals' (im) mobilization and bacterial health in soils., (Copyright © 2015 Elsevier B.V. All rights reserved.)

A hydrologically contained field study, to assess biochar (produced from mixed crop straws) influence upon soil hydraulic properties and dissolved organic carbon (DOC) leaching, was conducted on a loamy soil (entisol). The soil, noted for its low plant-available water and low soil organic matter, is the most important arable soil type in the upper reaches of the Yangtze River catchment, China. Pore size distribution characterization (by N2 adsorption, mercury intrusion, and water retention) showed that the biochar had a tri-modal pore size distribution. This included pores with diameters in the range of 0.1-10 μm that can retain plant-available water. Comparison of soil water retention curves between the control (0) and the biochar plots (16 t ha(-1) on dry weight basis) demonstrated biochar amendment to increase soil water holding capacity. However, significant increases in DOC concentration of soil pore water in both the plough layer and the undisturbed subsoil layer were observed in the biochar-amended plots. An increased loss of DOC relative to the control was observed upon rainfall events. Measurements of excitation-emission matrix (EEM) fluorescence indicated the DOC increment originated primarily from the organic carbon pool in the soil that became more soluble following biochar incorporation.

High concentration of toxic metals in military shooting range soils poses a significant environmental concern due to the potential release of metals, such as Pb, Cu, and Sb, and hence requires remediation. The current study examined the effectiveness of buffalo weed (Ambrosia trifida L.) biomass and its derived biochars at pyrolytic temperatures of 300 and 700 °C, natural iron oxides (NRE), gibbsite, and silver nanoparticles on metal immobilization together with soil quality after 1-year soil incubation. Destructive (e.g., chemical extractions) and non-destructive (e.g., molecular spectroscopy) methods were used to investigate the immobilization efficacy of each amendment on Pb, Cu, and Sb, and to explore the possible immobilization mechanisms. The highest immobilization efficacy was observed with biochar produced at 300 °C, showing the maximum decreases of bioavailability by 94 and 70% for Pb and Cu, respectively, which were attributed to the abundance of functional groups in the biochar. Biochar significantly increased the soil pH, cation exchange capacity, and P contents. Indeed, the scanning electron microscopic elemental dot mapping and X-ray absorption fine structure spectroscopic (EXAFS) studies revealed associations of Pb with P (i.e., the formation of stable chloropyromorphite [Pb5(PO4)3Cl]) in the biomass- or biochar-amended soils. However, no amendment was effective on Sb immobilization.

Recent investigations have shown frequent detection of pharmaceuticals in soils and waters posing potential risks to human and ecological health. Here, we report the enhanced removal of sulfamethazine (SMT) from water by physically activated biochar. Specifically, we investigated the effects of steam-activated biochars synthesized from an invasive plant (Sicyos angulatus L.) on the sorption of SMT in water. The properties and sorption capacities of steam-activated biochars were compared with those of conventional non-activated slow pyrolyzed biochars. Sorption exhibited pronounced pH dependence, which was consistent with SMT speciation and biochar charge properties. A linear relationship was observed between sorption parameters and biochar properties such as molar elemental ratios, surface area, and pore volumes. The isotherms data were well described by the Freundlich and Temkin models suggesting favorable chemisorption processes and electrostatic interactions between SMT and biochar. The steam-activated biochar produced at 700 °C showed the highest sorption capacity (37.7 mg g(-1)) at pH 3, with a 55% increase in sorption capacity compared to that of non-activated biochar produced at the same temperature. Therefore, steam activation could potentially enhance the sorption capacities of biochars compared to conventional pyrolysis., (Copyright © 2015 Elsevier B.V. All rights reserved.)

Limited mechanistic knowledge is available on the interaction of biochar with trace elements (Sb and As) that exist predominantly as oxoanions. Soybean stover biochars were produced at 300 °C (SBC300) and 700 °C (SBC700), and characterized by BET, Boehm titration, FT-IR, NMR and Raman spectroscopy. Bound protons were quantified by potentiometric titration, and two acidic sites were used to model biochar by the surface complexation modeling based on Boehm titration and NMR observations. The zero point of charge was observed at pH 7.20 and 7.75 for SBC300 and SBC700, respectively. Neither antimonate (Sb(V)) nor antimonite (Sb(III)) showed ionic strength dependency (0.1, 0.01 and 0.001 M NaNO3), indicating inner sphere complexation. Greater adsorption of Sb(III) and Sb(V) was observed for SBC300 having higher -OH content than SBC700. Sb(III) removal (85%) was greater than Sb(V) removal (68%). Maximum adsorption density for Sb(III) was calculated as 1.88 × 10(-6) mol m(-2). The Triple Layer Model (TLM) successfully described surface complexation of Sb onto soybean stover-derived biochar at pH 4-9, and suggested the formation of monodentate mononuclear and binuclear complexes. Spectroscopic investigations by Raman, FT-IR and XPS further confirmed strong chemisorptive binding of Sb to biochar surfaces., (Copyright © 2014 Elsevier Ltd. All rights reserved.)

Sulfamethazine (SMZ) is an ionizable and highly mobile antibiotic which is frequently found in soil and water environments. We investigated the sorption of SMZ onto soils amended with biochars (BCs) at varying pH and contact time. Invasive plants were pyrolyzed at 700 °C and were further activated with 30 % sulfuric (SBBC) and oxalic (OBBC) acids. The sorption rate of SMZ onto SBBC and OBBC was pronouncedly pH dependent and was decreased significantly when the values of soil pH increased from 3 to 5. Modeled effective sorption coefficients (K D,eff) values indicated excellent sorption on SBBC-treated loamy sand and sandy loam soils for 229 and 183 L/kg, respectively. On the other hand, the low sorption values were determined for OBBC- and BBC700-treated loamy sand and sandy loam soils. Kinetic modeling demonstrated that the pseudo second order model was the best followed by intra-particle diffusion and the Elovich model, indicating that multiple processes govern SMZ sorption. These findings were also supported by sorption edge experiments based on BC characteristics. Chemisorption onto protonated and ligand containing functional groups of the BC surface, and diffusion in macro-, meso-, and micro-pores of the acid-activated BCs are the proposed mechanisms of SMZ retention in soils. Calculated and experimental q e (amount adsorbed per kg of the adsorbent at equilibrium) values were well fitted to the pseudo second order model, and the predicted maximum equilibrium concentration of SBBC for loamy sand soils was 182 mg/kg. Overall, SBBC represents a suitable soil amendment because of its high sorption rate of SMZ in soils.

Veterinary antibiotics can be released to environment by the animals' excretions, which thereby poses human health and ecological risks. Six antibiotics (tetracycline, oxytetracycline, chlortetracycline, sulfamethazine, sulfamethoxazole, and sulfadimethoxine) at three concentrations (5, 10, and 20 mg kg(-1) soil) were employed in pots filled with a loamy sand upland soil. Three types of vegetable seedlings, including cucumber (Cucumis sativus), cherry tomato (Solanum lycopersicum), and lettuce (Lactuca sativa), were also cultivated during 45 d in the greenhouse. All antibiotics taken up by tested plants showed negative effects on growth. Relatively high levels of tetracyclines and sulfonamides (SAs) were detected in the nonedible parts, roots, and leaves of cucumber and tomato, but fruit parts accumulated them lower than acceptable daily intake. Indeed, cucumber roots accumulated SAs by up to 94.6% of total addition (at 5 mg kg(-1) soil).

Veterinary antibiotics are frequently detected in soils posing potential contamination of food crops. Sulfamethazine (SMT) uptake was investigated by lettuce (Lactuca sativa L.) grown in the soils treated with/without biochar derived from an invasive plant, burcucumber (Sicyos angulatus L.) (BBC700). Soils were contaminated with SMT at 5 and 50mgkg(-1), and treated with/without 5% BBC700 (ww(-1)). The lettuces were harvested after 5weeks of cultivation and were analyzed for SMT by a high performance liquid chromatography-tandem mass spectrometry after solid-phase extraction. With 5% BBC700, the uptake of SMT was reduced by 86% in the soil spiked with 5mgkg(-1) SMT compared to the control whereas a 63% reduction was observed in the soil spiked with 50mgkg(-1) SMT. Application of BBC700, into soils effectively reduced the SMT uptake by lettuce., (Copyright © 2014 Elsevier Ltd. All rights reserved.)

Sulfonamides (SAs) are one of the most frequently used antibiotics in the veterinary industry, showing high mobility in soils. Objectives of this research were to determine the sorption, distribution coefficients and involvement of different ionic forms of sulfamethazine (SMZ), a representative SAs, and to evaluate the transport of SMZ in biochar treated soils. Biochars were produced from an invasive plant, burcucumber (Sicyos angulatus L.), under slow pyrolysis conditions at peak temperatures of 300 °C (biochar-300) and 700 °C (biochar-700), respectively. The abilities of the biochars to retain SMZ in loamy sand and sandy loam soils were examined under different pHs and SMZ loadings. Soil column experiments were performed with and without biochars addition. Results showed that biochar-700 had a high degree of SMZ retention, with resultant decreased pH in both soils. Modeled effective sorption coefficients (KD,eff) values indicated that the observed high SMZ retention at pH 3 could be attributed to the π-π electron donor-acceptor interaction and electrostatic cation exchange, whereas at pH 5 and 7, cation exchange was the main mechanisms responsible. There was no temporal retardation of SMZ in biochar treated soil as compared to the untreated soil. However, biochar-700 treatment achieved up to 89% and 82% increase in the SMZ retention in sandy loam and loamy sand soils, respectively. The overall results demonstrated that burcucumber biochar produced at higher temperature was effective in reducing the mobility of SMZ in the studied soils., (Copyright © 2014 Elsevier Ltd. All rights reserved.)

Sulfamethazine (SMT) as a veterinary drug has been detected frequently in the environment. In this study, six biochars produced from tea waste (TW) at 300 and 700 °C with or without N2 and steam activation were characterized and evaluated for SMT sorption in water. The sorption of SMT was interpreted as a function of biochar production condition, SMT concentration, pH and physicochemical characteristics of biochar. Distribution coefficient data showed high sorption of SMT at low pH (∼3) and the highest sorption density of 33.81 mg g(-1) was achieved by the steam activated biochar produced at 700 °C. The steam activation process increased the adsorption capacity by increasing the surface area of the biochar. The π-π electron donor-acceptor interaction, cation-π interaction and cation exchange at low pH were the primary mechanisms governing SMT retention by biochars. Overall, steam activated tea waste biochar could be a promising remedy of SMT removal from water., (Copyright © 2014 Elsevier Ltd. All rights reserved.)

Ultramafic rocks and their related soils (i.e., serpentine soils) are non-anthropogenic sources of metal contamination. Elevated concentrations of metals released from these soils into the surrounding areas and groundwater have ecological-, agricultural-, and human health-related consequences. Here we report the geochemistry of four different serpentine soil localities in Sri Lanka by coupling interpretations garnered from physicochemical properties and chemical extractions. Both Ni and Mn demonstrate appreciable release in water from the Ussangoda soils compared to the other three localities, with Ni and Mn metal release increasing with increasing ionic strengths at all sites. Sequential extraction experiments, utilized to identify "elemental pools," indicate that Mn is mainly associated with oxides/(oxy)hydroxides, whereas Ni and Cr are bound in silicates and spinels. Nickel was the most bioavailable metal compared to Mn and Cr in all four soils, with the highest value observed in the Ussangoda soil at 168 ± 6.40 mg kg(-1) via the 0.01-M CaCl2 extraction. Although Mn is dominantly bound in oxides/(oxy)hydroxides, Mn is widely dispersed with concentrations reaching as high as 391 mg kg(-1) (Yudhaganawa) in the organic fraction and 49 mg kg(-1) (Ussangoda) in the exchangeable fraction. Despite Cr being primarily retained in the residual fraction, the second largest pool of Cr was in the organic matter fraction (693 mg kg(-1) in the Yudhaganawa soil). Overall, our results support that serpentine soils in Sri Lanka offer a highly labile source of metals to the critical zone.

Biochar is a stable carbon-rich by-product synthesized through pyrolysis/carbonization of plant- and animal-based biomass. An increasing interest in the beneficial application of biochar has opened up multidisciplinary areas for science and engineering. The potential biochar applications include carbon sequestration, soil fertility improvement, pollution remediation, and agricultural by-product/waste recycling. The key parameters controlling its properties include pyrolysis temperature, residence time, heat transfer rate, and feedstock type. The efficacy of biochar in contaminant management depends on its surface area, pore size distribution and ion-exchange capacity. Physical architecture and molecular composition of biochar could be critical for practical application to soil and water. Relatively high pyrolysis temperatures generally produce biochars that are effective in the sorption of organic contaminants by increasing surface area, microporosity, and hydrophobicity; whereas the biochars obtained at low temperatures are more suitable for removing inorganic/polar organic contaminants by oxygen-containing functional groups, electrostatic attraction, and precipitation. However, due to complexity of soil-water system in nature, the effectiveness of biochars on remediation of various organic/inorganic contaminants is still uncertain. In this review, a succinct overview of current biochar use as a sorbent for contaminant management in soil and water is summarized and discussed., (Copyright © 2013 Elsevier Ltd. All rights reserved.)

Few studies have investigated surface complexation of antimony (Sb) on natural sorbents. In addition, intrinsic acidic constants, speciation, and spectroscopic data are scarce for Sb sorption in soil. Only simple sorption models have been proposed to describe the sorption of Sb(V) on specific mineral surfaces. This study therefore assessed the mechanisms of Sb(III) and Sb(V) adsorption on natural red earth (NRE), a naturally occurring iron coated sand, at various pHs and Sb loadings. The Sb(V) adsorption followed typical anion adsorption curve with adsorption reaching maximum around pH 4-5, while no pH dependence was observed for Sb(III) sorption. The FT-IR spectra revealed that shifts in absorbance of the hydroxyl groups in iron-oxide were related to the Fe-O-Sb bonds and provided evidence for inner sphere bond formation. Direct evidence on the strong interaction of Sb(III) and Sb(V) with ≡Fe-O and ≡Al-O was observed from the decrease in Fe-2p, Al-2p, and Si-2p peaks of the X-ray photoelectron spectroscopy (XPS) data before and after Sb(V) and Sb(III) adsorption on NRE. Successful data modeling using the 2-pK diffuse double layer model (DDLM) with the FITEQL revealed that sorption occurs through the formation of bidentate mononuclear and binuclear complexes. Model simulations showed a high affinity to the ≡FeOH sites at high Sb loadings, whereas at low loadings, both≡ FeOH and ≡AlOH sites showed similar affinities to Sb. In the case of Sb(V), multilayer formation was also revealed in addition to surface complexation by the isotherm data fitted with the Freundlich model and two sites Langmuir equations, which indicated heterogeneous multilayer adsorption of Sb(V) on NRE., (Copyright © 2013 Elsevier Inc. All rights reserved.)

Chromium is abundantly and primarily present as Cr(III) in ultramafic rocks and serpentine soils. Chromium(III) oxidation involving chromite (FeCr2O4) via interactions with birnessite has been shown to be a major pathway of Cr(VI) production in serpentine soils. Alternatively, Cr(III)-bearing silicates with less Cr(III) may provide higher Cr(VI) production rates compared to relatively insoluble chromite. Of the potential Cr(III)-bearing silicates, Cr(III)-muscovite (i.e., fuchsite) commonly occurs in metamorphosed ultramafic rocks and dissolution rates may be comparable to other common Cr(III)-bearing phyllosilicates and clays. Here, we examine the formation of Cr(VI) related to Cr(III)-muscovite and birnessite (i.e., acid birnessite) interactions with and without humic matter (HM) via batch experiments. Experimentally, the fastest rate of Cr(VI) production involving Cr(III)-muscovite was 3.8 × 10(-1) μM h(-1) (pH 3 without HM). Kinetically, Cr(III)-muscovite provides a major pathway for Cr(VI) formation and Cr(VI) production rates may exceed those involving chromite depending on pH, available mineral surface areas in solution, and the abundance of Cr(III) present. However, when HM is introduced to the system, Cr(VI) production rates decrease by as much as 80%. This highlights that HM strongly decreases but may not completely suppress the formation and mobilization of Cr(VI). A Sri Lankan serpentine soil was utilized to provide context with regards to the experimental results. Despite Cr(VI) in the soil solids and Cr(VI) formation being favorable from Cr(III)-bearing minerals, no detectable Cr(VI) was released into soil solutions potentially due to the abundance of HM. Overall, the dynamic interactions of Cr(III)-bearing silicates and birnessite provide a kinetically favorable route of Cr(VI) formation which is tempered by humic matter.

In this study, pine needles were converted to biochar (BC) at different pyrolysis temperatures of 300, 500, and 700 °C to sorb trichloroethylene (TCE), and the changes in BC properties with each temperature were evaluated. Pyrolysis temperature showed a pronounced effect on BC properties. Decreases in molar H/C and O/C ratios resulted from removing O- and H-containing functional groups with increasing temperature, and produced high aromaticity and low polarity BCs. BCs produced at higher temperature showed greater TCE removal efficiency from water due to their high surface area, micro-porosity, and carbonized extent. The performance of various BCs for TCE removal was assessed by the Freundlich, Langmuir, Temkin, and Dubinin-Radushkevich adsorption models, among which the Temkin and Dubinin-Radushkevich models best described TCE adsorption onto various BCs, indicating prevailing sorption mechanism as pore-filling., (Copyright © 2013 Elsevier Ltd. All rights reserved.)