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We used an innovative approach involving hot pressing, low energy consumption, and no adhesive to transform bamboo biomass into a natural sustainable fiber-based biocomposite for structural and furniture applications. Analyses showed strong internal bonding through mechanical "nail-like" nano substances, hydrogen, and ester and ether bonds. The biocomposite encompasses a 10-fold increase in internal bonding strength with improved water resistance, fire safety, and environmentally friendly properties as compared to existing furniture materials using hazardous formaldehyde-based adhesives. As compared to natural bamboo material, this new biocomposite has improved fire and water resistance, while there is no need for toxic adhesives (mostly made from formaldehyde-based resin), which eases the concern of harmful formaldehyde-based VOC emission and ensures better indoor air quality. This surpasses existing structural and furniture materials made by synthetic adhesives. Interestingly, our approach can 100% convert discarded bamboo biomass into this biocomposite, which represents a potentially cost reduction alternative with high revenue. The underlying fragment riveting and cell collapse binding are obviously a new technology approach that offers an economically and sustainable high-performance biocomposite that provides solutions to structural and furniture materials bound with synthetic adhesives.

Hydrogen is recognized as one of the cleanest energy carriers, which can be produced from renewable biomass as a promising feedstock to achieve sustainable bioeconomy. Thermochemical technologies (e.g., gasification and pyrolysis) are the main routes for hydrogen production from biomass. Although biomass gasification, including steam gasification and supercritical water gasification, shows a high potential in field-scale applications, the selectivity and efficiency of hydrogen production need improvement to secure cost-effective industrial applications with high atom economy. This article reviews the two main-stream biomass-to-hydrogen technologies and discusses the significance of operating conditions and considerations in the catalytic system design. Challenges and prospects of hydrogen production via biomass gasification are explored to advise on the critical information gaps that require future investigations.

Selective removal of arsenic (As) is the key challenge for any of As removal mechanisms as this not only increases the efficiency of removal of the main As species (neutral As(III) and As(V) hydroxyl-anions) but also allows for a significant reduction of waste as it does not co-remove other solutes. Selective removal has a number of benefits: it increases the capacity and lifetime of units while lowering the cost of the process. Therefore, a sustainable selective mitigation method should be considered concerning the economic resources available, the ability of infrastructure to sustain water treatment, and the options for reuse and/or safe disposal of treatment residuals. Several methods of selective As removal have been developed, such as precipitation, adsorption and modified iron and ligand exchange. The biggest challenge in selective removal of As is the presence of phosphate in water which is chemically comparable with As(V). There are two types of mechanisms involved with As removal: Coulombic or ion exchange; and Lewis acid-base interaction. Solution pH is one of the major controlling factors limiting removal efficiency since most of the above-mentioned methods depend on complexation through electrostatic effects. The different features of two different As species make the selective removal process more difficult, especially under natural conditions. Most of the selective As removal methods involve hydrated Fe(III) oxides through Lewis acid-base interaction. Microbiological methods have been studied recently for selective removal of As, and although there have been only a small number of studies, the method shows remarkable results and indicates positive prospects for the future.

Refereed/Peer-reviewed Poly- and perfluoroalkyl substances (PFASs) are synthetic chemicals, which are introduced to the environment through anthropogenic activities. Aqueous film forming foam used in firefighting, wastewater effluent, landfill leachate, and biosolids are major sources of PFAS input to soil and groundwater. Remediation of PFAS contaminated solid and aqueous media is challenging, which is attributed to the chemical and thermal stability of PFAS and the complexity of PFAS mixtures. In this review, remediation of PFAS contaminated soils through manipulation of their bioavailability and destruction is presented. While the mobilizing amendments (e.g., surfactants) enhance the mobility and bioavailability of PFAS, the immobilizing amendments (e.g., activated carbon) decrease their bioavailability and mobility. Mobilizing amendments can be applied to facilitate the removal of PFAS though soil washing, phytoremediation, and complete destruction through thermal and chemical redox reactions. Immobilizing amendments are likely to reduce the transfer of PFAS to food chain through plant and biota (e.g., earthworm) uptake, and leaching to potable water sources. Future studies should focus on quantifying the potential leaching of the mobilized PFAS in the absence of removal by plant and biota uptake or soil washing, and regular monitoring of the long-term stability of the immobilized PFAS

Recently, there has been increasing interest in reducing methylmercury (MeHg) phytoavailability using biochar, although the underlying mechanisms are not fully understood. By combining lab-scale batch incubation with pot and field validations, we demonstrate that biochar-impacted sulfur cycling in soils and MeHg-soil binding play key roles in controlling MeHg phytoavailability. (1) Under anoxic conditions, biochar-associated sulfate and biochar-facilitated microbial sulfate reduction enhanced the production of reduced inorganic sulfur species as acid-volatile sulfide (AVS) in soils by 122%, facilitating MeHg binding with soils and thus reducing MeHg phytoavailability. (2) In contrast, under oxic conditions, the reduced inorganic sulfur was oxidized (resulting in a 68-91% decrease in AVS), which released soil-bound MeHg and increased MeHg phytoavailability. The proposed mechanisms could explain the distinct effects of biochar amendment on MeHg bioaccumulation observed under anoxic (10-88% lower in rice grains) and oxic conditions (48-84% higher in wheat grains). Our results dispute the commonly held assumption that reduced MeHg phytoavailability under biochar amendment can be primarily attributed to MeHg-biochar binding. Therefore, the potential increased risk of MeHg in oxic soils following biochar amendment should be evaluated in more detail.

Science of the Total Environment recently discussed how open access and predatory journals affect the flow of scientific knowledge in an unfortunate way. Now, South Korea's Ministry of Education is intervening to establish a system that will help its researchers avoid the growing global number of fake conferences of low academic and scientific merit. Here, we discuss solutions to this problem with respect to what is needed. Particularly, a list similar to that of Beall's for predatory conferences, without restricting researchers' academic freedom.

Soil lead (Pb) pollution is wide spread in China. The Chinese government is taking ambitious actions to tackle the soil pollution issue, with the latest soil quality standards and the Soil Pollutio...

Chromium (Cr) is a potentially toxic metal originating from natural processes and anthropogenic activities such as the iron-steel, electroplating, and leather industries, which is carcinogen to liv...

To effectively remove gaseous pollutants from air using sorbents, a thorough knowledge of the actual sorption performance is needed at ambient conditions rather than at unrealistically high-pressure conditions, as is commonly presented in the literature. To this end, the sorbent capacities of gaseous benzene were evaluated at a constant sorbent bed inlet pressure (50 ppm or ~5 Pa) in 1 atm of N 2 , room temperature (298 K), a fixed flow rate (50 mL min −1 ), and equal outlet sampling intervals (5 min). The benzene adsorption patterns were investigated against six sorbent types in a total of 17 different forms: 1- zeolite in five forms: beads (ZB), ground to 212 µm (ZG212), beads ground to 300 µm (ZG300), coarsely ground/washed zeolite (ZWc), and coarsely ground/washed/thermally treated zeolite (ZTc), 2- activated carbon in two forms: 212 µm (ACd212) and granular (ACdg), 3- Carbopack-X (CX), 4- Tenax TA (TA), 5- used black tea leaves of 150 or 300 µm in three forms: dry (TD150/TD300), wet (TW150/TW300), and wet dust (TWd), and 6- used ground coffee in either dry (CD) or wet forms (CW). Accordingly, the largest adsorption capacities at 5 Pa (e.g., >10 mg g −1 ) were observed for ACd212 (79.1) and ACdg (73.6). Moderate values (e.g., 5 −1 ) were obtained for ZG212 (7.98), CX (6.79), ZG300 (5.70), and ZB (5.58), while the remainder were far lower at −1 (e.g., tea leaves, ground coffee, TA, ZWc, and ZTc). The experimental benzene capacities of the tested sorbents were further assessed by the Langmuir, Henry's law, Freundlich, Dubinin-Radushkevich, and Elovich isotherm models. The linearized Langmuir adsorption isotherms of ACd212, ACdg, and CX showed the presence of more than one adsorption site (i.e., retrograde at the lowest pressures and two others at higher pressures). However, TA, zeolite, tea leaves, and ground coffee exhibited a type-V isotherm, wherein the sorption capacity continued to increase with loaded volume (i.e., multilayer adsorption). Thus, ACd212 has the best figure-of-merit based on a high 10% breakthrough volume (BTV) and low cost for real-world applications.

Aluminium-biochar composites (Al biochars) were devised to serve as a novel heterogeneous catalyst for isomerisation of glucose to fructose to achieve sustainable biorefineries. A series of Al biochars were synthesised from waste wood biomass, by varying the Al loading (10 or 20 wt%), pyrolysis temperature (from 500 to 750 °C), and purge gas (N2 or CO2). Their physicochemical properties, e.g., surface area, porosity, crystalline/amorphous structure, thermal stability, elemental composition, metal speciation, and acid/base site density, can be tuned by adjusting the pyrolysis conditions. As for their catalytic activity, 21.5 mol% fructose (selectivity 73.8 mol%) can be obtained from glucose conversion over Al biochar, after only 5 min heating at 160 °C in acetone/H2O as the medium. Such performance was comparable to those of costly advanced inorganic solid catalysts in the literature. Aluminium species in Al biochars were the major contributor of their catalytic activity, as fructose yield increased by 60% with increasing Al loading. In particular, active Al sites located on the biochar surface contributed to approximately 70% of the system activity, whilst the remainder was attributed to Al components leaching to the solution phase under hydrothermal conditions. The possible active species included Al2O3, Al(OH)3, AlO(OH), and Al–O–C moieties in amorphous phases, which may facilitate glucose isomerisation via the Lewis acid-driven mechanism (i.e., 1,2-hydride shift). This is the first study synthesising Al-biochar composites for catalytic glucose isomerisation, which demonstrates the high potential of biochar as a mesoporous and simple carbon support in emerging applications beyond environmental remediation.

We have developed a wood waste-derived biochar as a sustainable graphitic carbon catalyst for environmental remediation through catalytic pyrolysis under the synergistic effects between Cu heteroatoms and CO2, which for the first time are found to significantly enhance the oxygen functionalities, defective sites, and highly ordered sp2-hybridized carbon matrix. The copper-doped graphitic biochars (Cu-GBCs) were further characterized by XRD, FTIR, Raman, XPS, etc., revealing that the modified specific surface area, pore structure, graphitization, and active sites (i.e., defective sites and ketonic group) on the Cu-GBCs corresponded to the synergistic Cu species loading and Cu-induced carbon-matrix reformation in CO2 environment during pyrolysis. The catalytic ability of Cu-GBCs was evaluated using the ubiquitous peroxydisulfate (PDS) activation system for the removal of various organic contaminants (i.e., rhodamine B, phenol, bisphenol A, and 4-chlorophenol), and gave the highest degradation rate of 0.0312 min−1 in comparison with those of pristine GBCs and N2-pyrolyzed Cu-GBCs ranging from 0.0056 to 0.0094 min−1. The synergistic effects were attributed to the encapsulated Cu heteroatoms, evolved ketonic groups, and abundant unconfined π electrons within the carbon lattice. According to scavenger experiments, ESR analysis, and two-chamber experiments, selective and sustainable non-radical pathways (i.e., singlet oxygenation and electron transfer) mediated by the Cu-induced metastable surface complex were achieved in the Cu-GBC/PDS system. This study offers the first insights into the efficacy, sustainability, and mechanistic roles of Cu-GBCs as an emerging carbon-based catalyst for green environmental remediation.

In this study, a magnesium oxide (MgO) coated corncob biochar (MCB) was synthesized by pyrolyzing MgCl2 pretreated corncob, for a better performance in lead immobilization in a contaminated soil compared with corncob biochar (CB). The properties and microstructures of CB and MCB were investigated. It was observed that MgO particles ranging from 1 to 2 μm were well coated on MCB, and the MgO content in MCB was calculated at 29.90% in w/w. The surface area of the biochar was significantly enhanced from 0.07 to 26.56 m2/g after the MgO coating. The MgO coating also significantly facilitated the lead removal percentage from 23% to 74% in aqueous solution by biochar. CB failed to immobilize lead in a soil washing residue and could not reduce its environmental risks in a laboratory incubation study. In contrast, MCB was applied to the soil and resulted in a significant reduction in TCLP leached lead from 10.63 to 5.24 mg/L (reduced by 50.71%). The comparison between MCB and other amendments suggests that the biochar component of MCB adsorbed lead onto its surface through cation-π interaction and increased surface adsorption due to higher surface area, and then the MgO coated on MCB's surface further enhanced the adsorption through precipitation. The synergistic roles of biochar-mineral composites make them a promising candidate for soil remediation. Keywords: Engineered biochar, Magnesium oxide (MgO), Biochar-mineral composite, Lead immobilization, In situ stabilization, Soil remediation

Elevated levels of potentially toxic elements (PTEs) in aqueous environments have drawn attention recently due to their presence and toxicity to living beings. There have been numerous attempts to remove PTEs from aqueous media. The potential of metal–organic frameworks (MOFs) in removing PTEs from aqueous media has been recognized due to their distinctive advantages (e.g., increased removal capability, large surface area, adjustable porosity, and recyclability). Because of the poor stability of MOFs in water, pre and post synthetic modification and functionalization of MOFs have also been developed for water treatment investigations. This review addresses the performance and mechanisms of PTE removal in various modified MOFs in detail. In order to compare the performance of MOFs, here we used partition coefficient (PC) instead of maximum adsorption capacity, which is sensitively influenced by initial loading concentrations. Therefore, the PC of each material was used to evaluate the adsorption performance of different MOFs and to compare with other sorbents. Furthermore, it discusses the scale-up issues and forthcoming pathway for the research and development needs of MOFs for effective PTE removal. This review further elucidates the main removal mechanisms of PTEs by MOFs. Commercial or domestic water treatment systems or water filters can utilize engineered MOFs to treat water by adsorptive removal. However, marketable products have yet to be investigated thoroughly due to limitations of the large-scale synthesis of MOFs.

The assembly of two-dimensional (2D) nanosheets into three-dimensional (3D) well-organized superstructures is one of the key topics in materials chemistry and physics, due to their potential applications in various fields. Herein, starting from the crystalline metal-organic framework (MOF) particles, a spherical superstructure consisting of metal-organic framework nanosheets (SS-MOFNSs) is synthesized via a simple solvothermal transformation process. After pyrolysis and nitrogenization in ammonia, the SS-MOFNSs are further transformed into the spherical superstructure consisting of boron nitride nanosheets (SS-BNNSs), which preserve the original spherical superstructure morphology. Taking advantage of this unique superstructure, the resulting SS-BNNSs exhibit excellent catalytic activity for selective oxidative dehydrogenation of propane to produce propylene and ethylene. The results of this work provide a novel synthetic strategy to fabricate 3D spherical superstructures consisting of 2D nanosheets for high-performance applications in catalysis, energy storage, as well as other related fields.

In this study, a new photo-aging pathway in the aquatic environments and the underlying transformation mechanism were described for polyvinyl chloride microplastic (PVC-MP). Our results indicated that the photo-aging of PVC-MP was strongly dependent on particle size and the aging reaction could be facilitated in the presence of low-molecular-weight organic acid (LMWOA) and LMWOA-Fe(III) complex under simulated and natural sunlight irradiation and ambient conditions. The hydroxyl radical (OH•) generated from the photolysis of LMWOA or its ferric complexes played a dominant role in enhancing PVC-MP degradation. In situ Fourier transform infrared and Raman spectroscopic techniques and theoretical calculations further confirmed that C-Cl bond cleavage and formation of polyene and carbonyl underwent on the PVC-MP surface, especially in the presence of LMWOA and LMWOA-Fe(III). Moreover, PVC-MP surface oxidation also led to the increase of the specific surface area and affinity towards water as indicated by the results of scanning electron microscopy, Brunauer-Emmett-Teller tests and contact angles for water, which would further enhance the adsorption of polar contaminants on PVC-MP and thus increase the health risk of PVC-MP on aquatic organisms.

Eutrophication of natural water is a universal problem. Nitrogen (N) and phosphorus (P) from agricultural runoff are the main sources of nutrient input, provided that emissions from industrial point sources (IPS) are under control. Therefore, it is of great environmental importance to reduce pollution associated with agricultural runoff as a means of regulating eutrophication levels in natural water. Numerous methods proposed for treating agricultural runoff can be classified into three categories: source control, process control, and end treatment. In this review, major technologies for N and P control from agricultural runoff are summarized along with discussion of newly proposed technologies such as biochar biomimetics and microbial catalyst. Because agricultural runoff (from farmlands to receiving waters) is a complicated pollution process, it is difficult to regulate the nutrients discharged via such process. This review will thus offer a comprehensive understanding on the overall process of agricultural runoff and eutrophication to help establish control strategies against highly complicated agricultural non-point sources.

The ever-increasing rise in the global population coupled with rapid urbanization demands considerable consumption of fossil fuel, food, and water. This in turn leads to energy depletion, greenhouse gas emissions and wet wastes generation (including food waste, animal manure, and sewage sludge). Conversion of the wet wastes to bioenergy and biochar is a promising approach to mitigate wastes, emissions and energy depletion, and simultaneously promotes sustainability and circular economy. In this study, various conversion technologies for transformation of wet wastes to bioenergy and biochar, including anaerobic digestion, gasification, incineration, hydrothermal carbonization, hydrothermal liquefaction, slow and fast pyrolysis, are comprehensively reviewed. The technological challenges impeding the widespread adoption of these wet waste conversion technologies are critically examined. Eventually, the study presents insightful recommendations for the technological advancements and wider acceptance of these processes by establishing a hierarchy of factors dictating their performance. These include: i) life-cycle assessment of these conversion technologies with the consideration of reactor design and catalyst utilization from lab to plant level; ii) process intensification by integrating one or more of the wet waste conversion technologies for improved performance and sustainability; and iii) emerging machine learning modeling is a promising strategy to aid the product characterization and optimization of system design for the specific to the bioenergy or biochar application.

Conventional adsorbents for decontaminating arsenic exhibit low efficacy for the removal of arsenite (As(III)). This study aims to develop a robust As adsorbent from natural magnetite (M0) via a facile ball milling process, and evaluate their performance for decontaminating As(III) and As(V) in water and soil systems. The ball milling process decreased the particle size and crystallinity of M0, resulting in pronounced As removal by the ball-milled magnetite (Mm). Ball milling under air facilitated the formation of Fe-OH and Fe-COOH functional groups on Mm interface, contributing to effective elimination of As(III) and As(V) via hydrogen bonding and complexation mechanisms. Synergistic oxidation effects of hydroxyl and carboxyl groups, and reactive oxygen species (O2·-, and ·OH) on the transformation of As(III) to As(V) during the adsorption were proposed to explain the enhanced As(III) removal by Mm. A short-term soil incubation experiment indicated that the addition of Mm (10 wt%) induced a decrease in the concentration of exchangeable As by 30.25%, and facilitated the transformation of water-soluble As into residual fraction. Ball milling thus is considered as an eco-friendly (chemical-free) and inexpensive (scalable, one-stage process) method for upgrading the performance of natural magnetite towards remediating As, particularly for tackling the highly mobile As(III). Refereed/Peer-reviewed

In chelator-enhanced Zn phytoremediation studies, it is crucial to understand how the degradable chelators and the competition from other ions influence the concentration of Zn in soil solutions. This study investigated the biodegradability of two chelators (EDDS: Ethylenediamine-N,N'-disuccinic acid, and NTA: Nitrilotriacetic acid) and their effects on the Zn concentration in the soil solution during the growth of alfalfa (Medicago Sativa L.). The chelators were added at four doses (0, 0.5, 2 and 5 mmol kg

Improving the recovery of organic matter and phosphorus (P) from hazardous biowastes such as swine manure using acidic substrates (ASs) in conjunction with aerobic composting is of great interest. This work aimed to investigate the effects of ASs on the humification and/or P migration as well as on microbial succession during the swine manure composting, employing multivariate and multiscale approaches. Adding ASs, derived from wood vinegar and humic acid, increased the degree of humification and thermal stability of the compost. The 31P nuclear magnetic resonance spectroscopy and X-ray absorption near-edge structure analyses demonstrated compost P was in the form of struvite crystals, Ca/Al-P phases, and Poly-P (all inorganic P species) as well as inositol hexakisphosphate and Mono-P (organophosphorus species). However, the efficiency of P recovery could be improved by generating more struvite by adding the ASs. The flows among nutrient pools resulted from the diversity in the dominant microbial communities in different composting phases after introducing the ASs and appearance of Bacillus spp. in all phases. These results demonstrate the potential value of ASs for regulating and/or improving nutrients flow during the composting of hazardous biowastes for producing higher quality compost, which may maximize their beneficial benefits and applications.

The continuous growth of population and the steady improvement of people's living standards have accelerated the generation of massive food waste. Untreated food waste has great potential to harm the environment and human health due to bad odor release, bacterial leaching, and virus transmission. However, the application of traditional disposal techniques like composting, landfilling, animal feeding, and anaerobic digestion are difficult to ease the environmental burdens because of problems such as large land occupation, virus transmission, hazardous gas emissions, and poor efficiency. Pyrolysis is a practical and promising route to reduce the environmental burden by converting food waste into bioenergy. This paper aims to analyze the characteristics of food waste, introduce the production of biofuels from conventional and advanced pyrolysis of food waste, and provide a basis for scientific disposal and sustainable management of food waste. The review shows that co-pyrolysis and catalytic pyrolysis significantly impact the pyrolysis process and product characteristics. The addition of tire waste promotes the synthesis of hydrocarbons and inhibits the formation of oxygenated compounds efficiently. The application of calcium oxide (CaO) exhibits good performance in the increment of bio-oil yield and hydrocarbon content. Based on this literature review, pyrolysis can be considered as the optimal technique for dealing with food waste and producing valuable products.

The application of waste oils as pyrolysis feedstocks to produce high-grade biofuels is receiving extensive attention, which will diversify energy supplies and address environmental challenges caused by waste oils treatment and fossil fuel combustion. Waste oils are the optimal raw materials to produce biofuels due to their high hydrogen and volatile matter content. However, traditional disposal methods such as gasification, transesterification, hydrotreating, solvent extraction, and membrane technology are difficult to achieve satisfactory effects owing to shortcomings like enormous energy demand, long process time, high operational cost, and hazardous material pollution. The usage of clean and safe pyrolysis technology can break through the current predicament. The bio-oil produced by the conventional pyrolysis of waste oils has a high yield and HHV with great potential to replace fossil fuel, but contains a high acid value of about 120 mg KOH/g. Nevertheless, the application of CaO and NaOH can significantly decrease the acid value of bio-oil to close to zero. Additionally, the addition of coexisting bifunctional catalyst, SBA-15@MgO@Zn in particular, can simultaneously reduce the acid value and positively influence the yield and quality of bio-oil. Moreover, co-pyrolysis with plastic waste can effectively save energy and time, and improve bio-oil yield and quality. Consequently, this paper presents a critical and comprehensive review of the production of biofuels using conventional and advanced pyrolysis of waste oils.

In this study, biochar supported iron sulfide (FexSy) composite (FexSy@biochar) was synthesized and utilized as a persulfate (PS) activator for benzene removal from contaminated groundwater. The FexSy@biochar/PS system exhibited excellent performance in benzene adsorption and subsequent degradation. The optimal conditions for benzene removal in this study were found to be 1 g L-1 FexSy@biochar dosage and 3 mM PS concentration (removal rate 99.8%), with no reversible desorption of benzene concentrations in a long-time interval. The high catalytic performance of FexSy@biochar was mainly attributed to the free radicals (i.e., SO4•−,·OH) generated from PS activation induced by FexSy particles on biochar, followed by the possible activation by oxygen-containing groups. The as-prepared FexSy@biochar also showed long-term effectiveness for PS activation as confirmed by the 4 test cycled tests. The EPR not only demonstrated the presence of •OH and SO4•− free radicals but also indicated the sustainable release effect of reactive species from FexSy@biochar/PS system, as strong signals were observed in the FexSy@biochar/PS system even after 24 h. The FexSy@biochar could be an alternative to existing activators of in-situ chemical oxidation for contaminated groundwater remediation.

Pyrolysis of the middle layer of a surgical mask (MLM) and inner and outer layers of a surgical mask (IOM) was performed to assess their potential valorization as waste-to-energy feedstocks, and the characteristics of the resulting products were investigated. Pyrolysis of the main organics in waste surgical masks occurred at a very narrow temperature range of 456-466 °C. The main product was carbon-rich and oxygen-deficient liquid oil with a high heating value (HHV) of 43.5 MJ/kg. From the life-cycle perspective, environmental benefits and advantages of this upcycling approach were verified compared with conventional waste management approaches. This study advocated the potential application of waste surgical masks as feedstocks for fuels and energy, which is beneficial to mitigate plastic pollution and achieve sustainable plastic waste-to-energy upcycling, simultaneously.

Liquefaction is an attractive technology for converting biomass into bio-oil without the requirement for drying feedstock, and the process can be conducted at relatively low temperatures. In the practical application, the treated biomass feedstocks are composed of a mixture of agricultural waste, forestry waste and some organic solid waste. The utilization of co-liquefaction technology is suitable for biomass as it can fully utilize different types of feedstocks and enhance the liquefaction degree of each feedstock. During the co-liquefaction of these blending biomass feedstocks, the individual biomass species can degrade according to their own reaction network that is governed by the unique structural compositions. Furthermore, the reaction intermediates from the degradation of different biomasses can potentially interact with each other. This will affect the reaction characteristics and alter the chemical constituents and properties of the bio-oil produced. The understanding of interaction for the blending biomasses during the co-liquefaction process is of significance for tuning the chemical species and yield of the resulting bio-oil. Thus, this review work focuses on the co-liquefaction behavior of the various biomass feedstocks including lignocellulose, organic solid waste and algae. The influences of the essential operation parameters including solvent types, catalyst types, reaction temperature and time, and the mixing ratio of different biomasses on co-liquefaction behavior are also evaluated in detail. The choice of the proper reaction parameters is dependent on the structural characteristics of mixed feedstocks. Additionally, the co-liquefaction impact on the composition and formation mechanism of bio-oils are investigated.

Immense global generation of food waste calls for advanced technologies to maximize the use of such renewable carbon-based resources. In this study, corn, taro, lettuce, and bean sprout, were valorized for the production of value-added chemicals via sequential supercritical CO2 (scCO2) extraction and thermochemical conversion. The scCO2 extraction was performed at 350 bar and 50 °C for 60 min. The extracts of the lettuce contained sterols (764 μg g–1) that have potential anticancer properties. While bean sprout extracts had a higher content of saturated fatty acids (641 μg g–1), corn extracts comprised polyunsaturated fatty acids (405 μg g–1) as one of the major compounds, which are beneficial to cholesterol control. There were also notable amounts of wax esters (75–774 μg g–1) in these food waste extracts. Taro extracts were rich in both saturated (2313 μg g–1) and unsaturated fatty acids (1605 μg g–1) and, in particular, contained difatty acids that exhibit pharmaceutical activities. Moreover, the solid residues after scCO2 extraction served as the substrates for platform chemical production. The starch-rich substrates, i.e., taro and corn, resulted in 11–20% hydroxymethylfurfural (HMF) after microwave heating at 140 °C for 5–10 min using SnCl4 catalyst. In comparison, due to the high fiber content, lettuce and bean sprout required a higher temperature of 170–190 °C for chemical decomposition over H2SO4, generating a levulinic acid yield of ∼7%, in company with glucose and fructose as the coproducts. This study on the combined technologies suggested good compatibility between scCO2 extraction and subsequent thermochemical conversion, producing a wide spectrum of value-added chemicals from biomass waste. We herein highlight the vast potential of integrated technologies for food waste valorization in achieving sustainable and carbon-efficient biorefineries.

Syngas and biochar production are mainly influenced by temperature, feedstock properties, gasifying agent, pressure, and the mass ratio between gasifying agent and feedstock with temperature being the most significant factor. Increasing temperature generally promotes syngas production while suppressing biochar production. The selection of gasifiers (fixed bed, fluidized bed, and entrained flow) is highly dependent on scale requirement (e.g., volume of feedstock and energy demand), feedstock characteristics (e.g., moisture and ash content), and the quality of syngas and biochar. Updraft fixed bed gasifiers are suitable for the feedstocks with a moisture content up to 50 wt.%. High ash feedstocks such as Indian coal, dried sewage sludge, and municipal solid waste that are not suitable for fixed bed gasifiers, have been successfully gasified in bubbling fluidized bed reactors. Woody biomass is not suitable for entrained flow gasifiers unless specialized feeding methods are employed such as wood torre...

A series of organic acids, including maleic acid (maleicA), malic acid (malicA), succinic acid (SA), and oxalic acid (OA)/oxalate, was evaluated as green additives to promote the selective Al(III)-catalyzed production of hydroxymethylfurfural (HMF) from food waste. The roles of Al(III)–organic acid interactions in altering the catalytic functions were elucidated on the basis of experimental and computational evidence. The catalytic results showed that the Al/OA and Al/oxalate systems gave the slowest glucose conversion among the studied systems. OA/oxalate had such a high affinity for Al(III), that the Lewis acidity of Al(III) (i.e., ability to accept electron pairs) was unfavorably reduced, which was supported by the theoretical calculations of Gibbs free energies considering the Al(III)–OA complexes the most thermodynamically feasible. When rice waste was used as the substrate, which is rich in glucose-based starch, the addition of maleicA to the Al(III) system enhanced the HMF selectivity. The Lewis ac...

The impact of biochar (BC) application on soil varies with BC feedstock and soil type. The objective of this study was to investigate the linkage between the properties and surface functionality of various BCs and their role in the rehabilitation of two infertile soils. Sandy loam (SL) and sandy (S) soils were collected from agricultural areas in Korea and Vietnam, respectively. The BCs of amur silvergrass residue (AB), paddy straw (PB), and umbrella tree (UB) were applied to the soils at a rate of 30 t ha−1 and incubated at 25 °C for 90 d. Soil carbon (C) mineralization was investigated by a periodic measurement of CO2 efflux. Soil texture strongly influenced the CO2 efflux more than the BC type as indicated by 2–4 folds increase in cumulative CO2-C efflux from the SL soil compared to that from the S soil. For the PB-, AB-, and UB-treated S soils, the values of cation exchange capacity (CEC) were increased by 906%, 180%, and 130%, respectively, compared to that of the control; however, for the PB-treated SL soil, only a 13% increase in CEC was found. The pH in the PB-treated S soil sharply increased by 4.5 units compared to that in the control, due to a high concentration of readily soluble compounds in the PB and the low buffering capacity of the S soil. The S soil was more sensitive to the addition of BCs than the SL soil. A more prominent improvement in soil fertility can be achieved by BC application to the sandy soil having low clay, nutrient, and organic matter contents.

Human exposure to lead (Pb) is a growing global public health concern. Elevated blood lead is thought to cause the mental retardation of >0.6 million children globally each year, and has recently been attributed to ~18% of all-cause mortality in the US. Due to the severe health risk, the international community, led by the United Nations Environment Programme (UNEP) and the World Health Organization (WHO), is actively supporting the global phase-out of lead-based paint by 2020. However, there are many significant hurdles on the way to achieving this goal. In light of the importance of the lead-based paint issue, and the urgency of achieving the 2020 phase-out goal, this review provides critical insights from the existing scientific literature on lead-based paint, and offers a comprehensive perspective on the overall issue. The global production and international trade of lead-based paints across Asia, Africa, Latin America, and Europe are critically discussed – revealing that lead-based paints are still widely used in many low and middle-income developing countries, and that the production and trade of lead-based paint is still wide-spread globally. In India, as well as many south-east Asian, African, Latin American and European countries, lead concentrations in paints often exceed 10,000 mg/kg. This will certainly pose a serious global threat to public health from surfaces painted with these products for many decades to come. The sources and pathways of exposure are further described to shed light on the associated health risk and socioeconomic costs. Finally, the review offers an overview of the potential intervention and abatement strategies for lead-based paints. In particular, it was found that there is a general lack of consensus on the definition of lead based paint; and, strengthening regulatory oversight, public awareness, and industry acceptance are vital in combating the global issue of lead based paint. Keywords: Lead-based paint, Lead exposure, Blood lead level, Soil contamination

The catalytic activity of engineered biochar was scrutinized for generation of glucose and hydroxymethylfurfural (HMF) from starch-rich food waste (bread, rice, and spaghetti). The biochar catalysts were synthesized by chemical activation of pinewood sawdust with phosphoric acid at 400–600 °C. Higher activation temperatures enhanced the development of porosity and acidity (characterized by C O PO3 and C PO3 surface groups), which imparted higher catalytic activity of H3PO4-activated biochar towards starch hydrolysis and fructose dehydration. Positive correlations were observed between HMF selectivity and ratio of mesopore to micropore volume, and between fructose conversion and total acid density. High yields of glucose (86.5 Cmol% at 150 °C, 20 min) and HMF (30.2 Cmol% at 180 °C, 20 min) were produced from rice starch and bread waste, respectively, over H3PO4-activated biochar. These results highlighted the potential of biochar catalyst in biorefinery as an emerging application of engineered biochar.

Biochar has shown a unique electrochemical property being involved in various redox reactions in soil and water. In this study, the electron donating capacities (EDCs) of biochar pyrolyzed at 200–800 °C from pine wood, barley grass and wheat straw were investigated by using the mediated electrochemical oxidation method. The EDC values for all biochar were in the range of 0.18–1.83 mmol e− (g biochar)−1, showing the increase as the temperature increased from 200 °C to 400 °C, the decrease from 400 °C to 650 °C, and then increase from 650 °C until to 800 °C. At low and intermediate temperatures of 200–650 °C, the EDCs were mainly attributed to the phenolic hydroxyl groups, while the conjugated π-electron system associated with aromatic structure dominated the EDCs of biochar at the high temperatures of over 650 °C. The barley grass- and wheat straw-derived biochar had higher EDCs than the pine wood-derived biochar, resulting from the higher phenolic hydroxyl groups in the former samples than the latter one. In conclusion, the reductive property of biochar was mainly attributed to both phenolic hydroxy group and conjugated π-electron system associated with aromatic structure, depending on the pyrolytic temperature and feedstock source. The results will help us to obtain a complete view on the role of biochar in biogeochemical redox reactions and consider developing biochar with controlled redox properties for specific environmental applications such as electron shuttle and catalyst material.

This study is a comparison of the effect of biochar produced by bioenergy systems, via the pyrolysis and gasification processes, on the immobilization of metals/metalloids in soil. Because the processes for these two techniques vary, the feedstocks undergo different heating regimens and, as a result, their respective char products exhibit different physico-chemical properties. Therefore, this study focuses on (1) the characterization of derivative biochar from the bioenergy system to understand their features and (2) an exploration of various biochar impacts on the mobility of As and Pb in contaminated soil. The results showed bioenergy biochars (BBCs) performed well in mitigating Pb extractability (1 M ammonium acetate) with a Pb immobilization >80%, but unfavorably mobilized the bioavailable As, likely because of electrostatic repulsion and ion exchange competition. The BBC surface functional group would chemically bond with the As and remain stable against the pH change. An increment in aromatic carbon would effectively enhance cation-π interaction for Pb immobilization. Nevertheless, an amendment with richer condensed structure and higher inorganic minerals (Ca2+, K+, Mg2+, and Na+) can lead to better performance in retaining Pb.

In this work, glucose isomerization to fructose was conducted via a solid base biochar catalyst derived from spent coffee grounds and melamine. The X-ray photoelectron spectroscopy spectra identified the majority of pyridinic nitrogen on the biochar surface, which imparted the strong base character of the catalyst. Activity of the catalyst was evidenced by fast conversion of glucose (12%) and high selectivity to fructose (84%) in 20 min at a moderate temperature (120 °C) compared to recently reported immobilized tertiary amines at comparable N concentrations (10–15 mol % relative to glucose). By increasing the reaction temperature to 160 °C, fructose yield achieved 14% in 5 min. The base biochar catalyst showed superior selectivity (>80%) to commonly used homogeneous base catalysts, such as aqueous hydroxides and amines (50–80%) and comparable catalytic activity (∼20 mol % conversion within 20 min). Moreover, cosolvent of acetone in the reaction system may increase the overall basicity by stabilizing prot...

Engineered biochars were prepared by slow pyrolysis of three types of biomass pretreated with eggshell waste. The resulting biochars were composite materials with eggshell particles on carbon surface within the pore networks, which were confirmed by various characterization tools. The engineered biochars showed relatively fast adsorption kinetics to Pb 2+ aqueous solutions. In addition, adsorption isotherms showed that the Langmuir maximum Pb 2+ adsorption capacities of the engineered biochars (103–261 mg/g) were higher than those of the pristine biochars (32.9–56.0 mg/g). The adsorption of Pb 2+ onto the biochars were affected by adsorbent dosage, initial solution pH, and ionic strength. Findings from this work indicated that the engineered biochar from eggshell-treated biochar can be used as an effective agent for soil and water remediation and conservation.

In the recent techno-scientific revolution, nanotechnology has gained popularity at a rapid pace in different sectors and disciplines, specifically environmental, sensing, bioenergy, and agricultural systems. Controlled, easy, economical, and safe synthesis of nanomaterials is desired for the development of new-age nanotechnology. In general, nanomaterial synthesis techniques, such as chemical synthesis, are not completely safe or environmentally friendly due to harmful chemicals used or to toxic by-products produced. Moreover, a few nanomaterials are present as by-product during washing process, which may accumulate in water, air, and soil system to pose serious threats to plants, animals, and microbes. In contrast, using plants for nanomaterial (especially nanoparticle) synthesis has proven to be environmentally safe and economical. The role of plants as a source of nanoparticles is also likely to expand the number of options for sustainable green renewable energy, especially in biorefineries. Despite several advantages of nanotechnology, the nano-revolution has aroused concerns in terms of the fate of nanoparticles in the environment because of the potential health impacts caused by nanotoxicity upon their release. In the present panoramic review, we discuss the possibility that a multitudinous array of nanoparticles may find applications convergent with human welfare based on the synthesis of diverse nanoparticles from plants and their extracts. The significance of plant-nanoparticle interactions has been elucidated further for nanoparticle synthesis, applications of nanoparticles, and the disadvantages of using plants for synthesizing nanoparticles. Finally, we discuss future prospects of plant-nanoparticle interactions in relation to the environment, energy, and agriculture with implications in nanotechnology.

In this review, we scrutinized novel synthetic recipes for the fabrication of nanomaterials derived from various biowastes including crop residue, food waste, and industrial waste (e.g., spent battery waste and polythene waste). To this end, various pretreatment methods have been developed and applied for the conversion of wastes into useful forms of nanomaterials (e.g., metallic/carbon nanoparticles, carbon nanotubes/nanosheets, and nanoactivated carbon) via chemical and thermal activation, arc discharge, vacuum evaporation-inert gas condensation, sodium borohydride reduction and solvent thermal approaches. Possible utilization of the waste-derived nanomaterials in various fields is discussed in detail including environmental remediation, bio-imaging, sensing, and energy storage by exploring their catalytic and fluorescence activities. Possible detrimental impact of using nanomaterials on living system is also highlighted. Lastly, our review emphasizes various aspects of an upcoming research areas which will be beneficial for further research.

Platform chemicals such as hydroxymethylfurfural (HMF) can be obtained through the conversion of biomass with the aid of metal catalyst (i.e., Cr(III) or Sn(IV)) systems. In this study, we examined the use of an environmentally compatible cocatalyst, namely, maleic acid (MA), to regulate the reaction kinetics and product selectivity in the metal-catalyzed conversion of rice waste to HMF. The maximum yields of HMF by Sn(IV) and Cr(III) systems were ∼36 and ∼26 mol %, respectively, in a medium of dimethyl sulfoxide (DMSO)/H2O at 140 °C. The addition of MA to Sn(IV) system did not noticeably alter the conversion kinetics. In contrast, MA significantly changed the kinetics in the Cr(III) system, reducing the rate of glucose isomerization, while accelerating starch hydrolysis. The latter may be ascribed to the increased accessibility of starch, as malic acid (38.4%) emerging from hydration of MA in the Cr(III) system could have interrupted the hydrogen bond network of starch. HMF selectivity was also enhanced ...

This study investigated the use of 30 w/v% H2SO4 sulfonated wood waste-derived biochar as catalysts for production of value-added chemicals from carbohydrates in water as an environmentally benign solvent. Physicochemical characteristics of the sulfonated biochar were revealed by Fourier transform infrared spectroscopy (FTIR), acid-base neutralization titration, gas adsorption analysis, thermogravimetric analysis (TGA), and scanning electron microscopy with energy dispersive X-ray spectroscopy (SEM-EDX). Using the sulfonated biochar as catalysts, hydrolysis of maltose at 140–160 °C resulted in the maximum glucose yield of 85.4% and selectivity of 88.2%, whereas dehydration of fructose at 160–180 °C produced the maximum HMF yield of 42.3% and selectivity of 60.4%. A higher range of reaction temperature was required for fructose dehydration due to the higher energy barrier compared to maltose hydrolysis. While increasing the temperature accelerated the catalytic reactions, the maximum product selectivity remained unchanged in the sulfonated biochar-catalyzed systems. The products were stable despite the increase in reaction time, because rehydration and adsorption of products was found to be minor although polymerization of intermediates led to unavoidable carbon loss. This study highlights the efficacy of engineered biochars in biorefinery as an emerging application.

This study compared the effects of sewchar and mineral fertilizer on plant responses in beans (Phaseolus vulgaris, var. “Jalo precoce”) and soil properties in a pot experiment in a completely randomized design with two harvests. The initial treatments consisted of a control, sewchar doses of 4, 8, 16 and 32 Mg ha−1 and mineral fertilizer (30 mg N, 90 mg P2O5 and 60 mg K2O kg−1). The treatments (4 replications each) were fertilized with 135 mg P2O5 kg−1 at the second harvest. The sewchar application rates correlated positively with the CEC, the water holding capacity, the availability of Zn, Ca, Fe, Cu, and P, and the concentrations of nitrate, ammonium, total N, total organic carbon and hot water extractable carbon. They correlated negatively with the Mg availability and the soil C: N ratio. Additionally, they correlated positively with the P, Zn and Ca uptake from the soil. For both harvests, the 16 Mg ha−1 sewchar treatment had a total dry matter equivalent to that of the mineral fertilizer. After the second harvest, the 16 Mg ha−1 sewchar treatment revealed 96% higher plant biomass than the control and 79% higher biomass than it did during the first period. The positive effect of sewchar in addition to phosphorous on the plant response and soil properties suggests that the residual effect of sewchar could be a promising alternative as a soil amendment for partly replacing mineral fertilizers. In future, further studies are necessary to evaluate long-term residual effects of sewchar in soil.

In the present investigation, poultry manure and farmyard manure-derived biochars were applied as cost-effective adsorbents for manganese (Mn) removal from aqueous media. Effects of functional parameters such as solution pH, contact time, temperature and concentration on the Mn removal efficiency of biochars were evaluated. Poultry manure-derived biochar exhibited greater adsorption efficiency than farmyard manure-derived biochar due to its porosity and surface functionality. The maximum adsorption was achieved at pH 6, temperature 298 K and contact time of 3 h. The adsorption isotherm data was well fitted to the Freundlich model indicating multilayer adsorption onto heterogeneous surfaces of the biochars. Thermodynamics calculations affirmed that Mn adsorption onto biochars was spontaneous and exothermic process governed by hydrogen bonding type of electrostatic interaction. Post-adsorption spectroscopic analysis of Mn-loaded biochars evidenced the binding of Mn with active surface functionalities of biochars.

For removing potentially toxic elements (PTEs) from field-contaminated soils, cost-effective soil remediation has been a worldwide concern. As one of the widely employed techniques, chelant-enhanced phytoremediation can remove PTEs with marginal impact on the soil properties, yet the newly formed metal-chelant complexes cannot be completely captured and extracted by the plants. This arouses concerns about downstream migration and secondary contamination of the metal-chelant complexes and free chelant. Organic amendments, such as food waste compost (FWC), may stabilize metals and/or metal-chelant complexes, improve soil properties and plant growth, and reduce waste volume. Therefore, FWC may provide a solution for the migration of metal-chelant complexes and free chelant. Two chelants were selected in this study: EDTA (ethylene-diaminetetraacetic-acid) and its biodegradable isomer EDDS ([S,S]-ethylenediaminedisuccinic acid). The interactions between FWC and metals, metal-EDTA/metal-EDDS complexes in a field-contaminated soil (mainly by Cu, Zn, and Pb) were investigated. Batch adsorption isotherms indicated a strong adsorption capacity of FWC for uncomplexed Cu, Zn, and Pb ions. Significant adsorption of Pb-EDDS (∼100%), Zn-EDDS (>77%), and Cu-EDTA (36–76%) complexes on the FWC was found at apparent equilibrium. The adsorption capacity of Cu-EDDS (32–38%), Pb-EDTA (∼20%), and Zn-EDTA (∼0%) complexes was limited. However, the co-existence of FWC and EDDS increased the mobilization of Cu and Zn, while the co-existence of FWC and EDTA reduced the available amounts of Cu and Pb in solution. Metal speciation calculation showed that nearly all extracted Cu, Zn, and Pb were complexed with chelants in the solution, while notable amount of dissolved Fe (but not Al and Ca) was associated with dissolved organic matter. In this study, FWC can be useful for minimizing the unintended leaching of Cu- and Pb-EDTA complexes in EDTA-enhanced phytoremediation, yet it might be less suitable for the case of EDDS. A novel integration of recycled waste can enhance the effectiveness of sustainable remediation of contaminated soils.

The removal of recalcitrant organic pollutants in groundwater is a challenge being faced around the world. Achieving effective long-term remediation of contaminated aquifers faces a variety of significant issues such as back diffusion, tailing, and rebound. In recent years, some researchers have proposed the use of controlled release materials (CRMs) as a new approach to counteracting such issues. The novelty of CRMs lies in that they release their active products slowly, over prolonged periods of time, in order to sustain in situ treatments and long-term effectiveness. Here we review the main constituents of CRMs, analyze their production, characterization, and applications, with a focus on reaction mechanisms, effectiveness, and secondary effects. This review shows that the reactive components of CRMs most commonly involve either: (i) chemical oxidants to treat contaminants such as TCE, PCE, BTEX, and 1,4-Dioxane; (ii) sources of dissolved oxygen to stimulate aerobic biodegradation of contaminants such as BTEX and 1,4-Dioxane; or, (iii) substrates that stimulate reductive dechlorination of contaminants such as TCE and 1,2-DCA. It was found that in some studies, CRMs provided sustained delivery of CRM treatment reagents over several years, and achieved complete contaminant removal. However, lower removal rates were apparent in other cases, which may be ascribed to insufficient dispersion in the subsurface. There are a relatively limited number of field-scale applications of CRMs in contaminated land remediation. Those conducted to date suggest that CRMs could prove to be an effective future remediation strategy. Lessons learned from field applications, suggestions for future research directions, and conclusions are put forward in this review.

Chelant-enhanced soil washing, such as EDTA (ethylenediaminetetraacetic acid) and biodegradable EDDS ([S,S]-ethylene-diamine-disuccinic acid), has been widely studied, however, EDTA is persistent under natural conditions while EDDS has a low efficiency for Pb extraction. Therefore, we investigated the efficacy of mixed chelants (EDDS and EDTA mixture at 1:1 M ratio) for the removal of Cu, Zn, and Pb from a field-contaminated soil using various washing schemes (multi-pulse, step-gradient chelant, and continuous washing schemes). Speciation modelling of the target metals, mineral elements, and EDDS/EDTA was performed, while the leachability and bioaccessibility of residual metals in the treated soils were also assessed. Our results suggested that the combined use of EDDS and EDTA reached equivalent extraction efficiency of the target metals as EDTA, i.e., 50% reduction in the dosage of EDTA was made possible. This was accomplished by selective extraction of Cu by EDDS and Pb by EDTA, which was supported by the results of speciation calculation. Multi-pulse washing scheme with intermittent water rinsing steps removed entrapped metal-chelant complexes and free chelants, therefore reducing the leachability and bioaccessibility of residual metals in the treated soils. Step-gradient chelant washing with the maximum dosage of chelants in the first washing step only achieved marginal improvement but undesirably promoted Pb bioaccessibility. Continuous washing for 24 h enhanced metal extraction but promoted mineral dissolution, together with a large amount of uncomplexed chelants and increase in Cu leachability. Thus the combined use of EDDS and EDTA in multi-pulse washing is recommended for further studies.