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Increased urbanization and industrialization accelerated demand for energy, large-scale waste output, and negative environmental consequences. Therefore, the implementation of an effective solid-waste-management (SWM) policy for the handling of food waste is of great importance. The global food waste generation is estimated at about 1.6 gigatons/yr which attributes to an economic revenue of 750 billion USD. It can be converted into high-value enzymes, surfactants, Poly-hydroxybutyrate, biofuels, etc. However, the heterogeneous composition of food with high organic load and varying moisture content makes their transformation into value-added products difficult. This review aims to bring forth the possibilities and repercussions of food waste management. The socio-economic challenges related to SWM are comprehensively discussed particularly in terms of environmental concern. The engineering aspect in the collection, storage, and biotransformation of food waste into useful value-added products such as biofuels, advanced biomaterials, bioactive compounds, and platform chemicals are critically reviewed for efficient food waste management.

The contamination of marine sediments by 4-nonylphenol (4-NP) has become a global environmental problem, therefore there are necessaries searching appropriate and sustainable remediation methods for in-situ applications. Herein, water hyacinth [(WH) (Eichhornia crassipes)]-derived metal-free biochar (WHBC) prepared at 300-900 °C was used to promote the calcium peroxide (CP)-mediated remediation of 4-NP-contaminaed sediments. At [CP] = 4.37 × 10

The accumulation of pollutants in the semi-enclosed waters of ports has long been a concern. This study assessed the pollution status, sources, and toxicity risks of 16 polycyclic aromatic hydrocarbons (PAHs) in surface sediments of 7 major ports in Taiwan. Total PAHs concentrations in sediments ranged between 8.4 and 572.5 ng/g dw, with an average of 112.4 ± 136.5 ng/g dw. The 3- and 4-ring PAHs (63 %) were the major constituents of PAHs in the sediments. Diagnostic ratios and positive matrix factorization analyses indicated that PAHs in sediments were mainly contributed by biomass combustion (45.0 %), coal combustion (31.5 %), and vehicle emissions and related fossil fuels (23.5 %). The results of ecological risk assessment showed a low-medium risk of PAHs in the sediments outside the port, whereas most of the sediments within the port presented a medium-high risk. An assessment of the possible human health risks indicated that PAHs were present at acceptable levels.

Seawater, sediments, and three genera of wild scleractinian corals were collected from four coral reef areas nearshore Liuqiu Island, southwestern Taiwan. Abundance, characteristics (sizes, colors, shapes, and polymer types), and enrichment of microplastics (MPs) in the corals, and their impacts on coral cover were determined. The average MPs abundances were 0.95, 0.77, and 0.36 item/g for Galaxea sp, Acropora spp, and Pocillopora sp, respectively. The MPs abundance was relatively higher on the coral surfaces than inside the skeletons, dominated by blue rayon-fibers, correspondingly observed in seawater and sediments. Large-size colorless MPs tended to be mis-ingested by Galaxea sp. (71%) compared with Pocillopora sp. (43%) and Acropora spp. (31%). The low hard coral cover (12.5%) observed at Yufu (L1) on the northeastern coastal zone nearby tourism center of Liuqiu Island where correspondingly associated with high MPs abundance in seawater (10 item/L), sediments (260 item/kg), and corals (0.60 item/g). Tourism induced sewage discharges and sailing activities significantly contributed to the MPs pollution, probably contributing to the loss of coral cover. High MPs enrichment in corals (EF

The present report investigates the various MoO

Phthalate esters (PAEs) are a group of ubiquitous organic environmental contaminants. Engineered ferromanganese-bearing sludge-derived biochar (SDB), synthesized using one-step pyrolysis in the temperature range between 300 and 900 °C, was used to enable Fenton-like processes that decontaminated PAE-laden sediments. SDB was thoroughly characterized using scanning electron microscopy energy-dispersive spectroscopy, transmission electron microscopy, Brunauer–Emmett–Teller surface area, thermogravimetric analysis, Raman spectroscopy, Fourier-transform infrared spectroscopy, electron paramagnetic resonance, X-ray photoelectron spectroscopy, and fluorescence excitation–emission matrix spectroscopy coupled with parallel factor analysis. The maximum PAE degradation was remarkable at 90% in 12 h at pH 6.0 in the presence of 1.7 g L−1 of SDB 900. The highly-effective PAE degradation was mainly attributed to the synergism between FeOx and MnOx, which strengthened the activation of percarbonate (PC) via electron transfer, hydroxy addition, and hydrogen abstraction through radical (HO•) and nonradical (1O2) oxidation mechanisms, thereby facilitating PAE catalytic degradation over SDB in real sediments, which clearly proved the efficacy of ferromanganese-bearing SDB and PC for the remediation of contaminated sediments. The cytotoxicity exhibited by human skin keratinocyte cells exposure to high SDB concentration (100–400 µg mL−1) for 24–48 h was low indicating insignificant cellular toxicity and oxidative damages. This study provides a new strategy for freshwater sludge treatment and reutilization, which enables a water-cycle-based circular economy and waste-to-resource recycling.

Managing the concentration of atmospheric CO2 requires a multifaceted engineering strategy, which remains a highly challenging task. Reducing atmospheric CO2 (CO2R) by converting it to value-added chemicals in a carbon neutral footprint manner must be the ultimate goal. The latest progress in CO2R through either abiotic (artificial catalysts) or biotic (natural enzymes) processes is reviewed herein. Abiotic CO2R can be conducted in the aqueous phase that usually leads to the formation of a mixture of CO, formic acid, and hydrogen. By contrast, a wide spectrum of hydrocarbon species is often observed by abiotic CO2R in the gaseous phase. On the other hand, biotic CO2R is often conducted in the aqueous phase and a wide spectrum of value-added chemicals are obtained. Key to the success of the abiotic process is understanding the surface chemistry of catalysts, which significantly governs the reactivity and selectivity of CO2R. However, in biotic CO2R, operation conditions and reactor design are crucial to reaching a neutral carbon footprint. Future research needs to look toward neutral or even negative carbon footprint CO2R processes. Having a deep insight into the scientific and technological aspect of both abiotic and biotic CO2R would advance in designing efficient catalysts and microalgae farming systems. Integrating the abiotic and biotic CO2R such as microbial fuel cells further diversifies the spectrum of CO2R.

A sensitive voltammetric sensor has been developed for hazardous methyl parathion detection (MP) using graphene oxide@Ce-doped TiO2 nanoparticle (GO@Ce-doped TiO2 NP) electrocatalyst. The GO@Ce-doped TiO2 NPs were prepared through the sol-gel method and characterized by various physicochemical and electrochemical techniques. The GO@Ce-doped TiO2 NP–modified glassy carbon electrode (GCE) addresses excellent electrocatalytic activity towards MP detection for environmental safety and protection. The developed strategy of GO@Ce-doped TiO2 NPs at GCE surfaces for MP detection achieved excellent sensitivity (2.359 μA μM−1 cm−2) and a low detection limit (LOD) 0.0016 μM with a wide linear range (0.002 to 48.327 μM). Moreover, the fabricated sensor shows high selectivity and long-term stability towards MP detection; this significant electrode further paves the way for real-time monitoring of environmental quantitative samples with satisfying recoveries.

Freshwater demand is rising worldwide due to largely increasing population and industrialization. Latest focus is to explore the Ocean and saline effluent from industries to produce freshwater in a sustainable way via algal desalination. Current physicochemical desalination technology is not only an energy-intensive and expensive process but also gives severe environmental impact from brine and GHGs emissions. Therefore, it is neither environmentally-friendly nor feasible to countries with limited resources. Biodesalination could be an attractive technology with recent breakthroughs in algal bioprocess with fast growth rate under highly saline conditions to effectively remove salts optimally 50–67% from saline water. Algal desalination mainly occurs through biosorption and bioaccumulation which governs by biotic and abiotic factors e.g., strain, temperature, pH, light and nutrients etc. This review provides a current scenario of this novel technology by an in-depth assessment of technological advancement, social impact, possible risks and scope for policy implications.

Biochar is a carbon-rich material prepared from the pyrolysis of biomass under various conditions. Recently, biochar drew great attention due to its promising potential in climate change mitigation, soil amendment, and environmental control. Obviously, biochar can be a beneficial soil amendment in several ways including preventing nutrients loss due to leaching, increasing N and P mineralization, and enabling the microbial mediation of N2O and CO2 emissions. However, there are also conflicting reports on biochar effects, such as water logging and weathering induced change of surface properties that ultimately affects microbial growth and soil fertility. Despite the voluminous reports on soil and biochar properties, few studies have systematically addressed the effects of biochar on the sequestration of carbon, nitrogen, and phosphorus in soils. Information on microbially-mediated transformation of carbon (C), nitrogen (N), and phosphorus (P) species in the soil environment remains relatively uncertain. A systematic documentation of how biochar influences the fate and transport of carbon, phosphorus, and nitrogen in soil is crucial to promoting biochar applications toward environmental sustainability. This report first provides an overview on the adsorption of carbon, phosphorus, and nitrogen species on biochar, particularly in soil systems. Then, the biochar-mediated transformation of organic species, and the transport of carbon, nitrogen, and phosphorus in soil systems are discussed. This review also reports on the weathering process of biochar and implications in the soil environment. Lastly, the current knowledge gaps and priority research directions for the biochar-amended systems in the future are assessed. This review focuses on literatures published in the past decade (2009–2021) on the adsorption, degradation, transport, weathering, and transformation of C, N, and P species in soil systems with respect to biochar applications.

Lytic polysaccharide monooxygenases (LPMOs) emerged a decade ago and have been described as biomass deconstruction boosters as they play an extremely important role in unravelling the enzymatic biomass hydrolysis scheme. These are oxidative enzymes requiring partners to donate electrons during catalytic action on cellulose backbone. Commercial cellulase preparations are mostly from the robust fungal sources, hence LPMOs from fungi (AA9) have been discussed. Characterisation of LPMOs suffers due to multiple complications which has been discussed and challenges in detection of LPMOs in secretomes has also been highlighted. This review focuses on the significance of LPMOs on biomass hydrolysis due to which it has become a key component of cellulolytic cocktail available commercially for biomass deconstruction and its routine analysis challenge has also been discussed. It has also outlined a few key points that help in expressing catalytic active recombinant AA9 LPMOs.

The presence of ultrafine plastics particles and its potential to concentrate and transport organic contaminants in aquatic environments have become a major concern in recent years. Specifically, the uptake of hazardous chemicals by plastics particles may affect the distribution and bioavailability of the chemicals. In this study, the adsorption of tetracycline (TC), an antibiotic frequently found in aquatic environments, on high-density polyethylene (PE) particles with the average size of 45 μm, was investigated. The PE particles were characterized for surface acidity for the first time. Results showed that pH controls the surface charge of PE particles. TC adsorption onto PE particles was rapid as expected following the pseudo-second-order rate law (r2 > 0.99). Polar forces in addition to specific chemical interactions, such as hydrogen bonding and hydrophophilicity controlled TC adsorption onto PE particles. Parameters, including pH, dissolved organic matter, ionic strength, major cations and anions affected TC adsorption onto PE micro-particles. Results indicated that PE particles can function as a carrier of antibiotics in the aquatic environment, which potentially imposes ecosystem and human health risks.

Sediment is an important final repository of persistent organic pollutants such as polycyclic aromatic hydrocarbons (PAHs). Herein, a novel catalyst of LaFeO

There has been growing research interest in exploiting biochar for cost-effective. removal of different pollutants. Heavy metals, especially copper II (Cu II) is highly toxic and nonbiodegradable pollutants, and has been major source of environmental pollution. In this study adsorption of Cu (II) on seaweed (Ascophyllum nodosum)-derived biochar was systematically examined. The removal efficiency based on surface property of biochar and type of interactions associated with biochar produced at varying pyrolysis conditions were investigated. The highest removal efficiency of Cu (II) from aqueous media was >99% with 223 mg g−1 Cu (II) adsorption capacity observed by biochar derived at 700 °C and pH 5. Langmuir adsorption isotherm described the adsorption mechanisms of Cu (II) on biochar with cationic and anionic electrostatic attractions, surface precipitation, and pore depositions. Thus, this study shows that waste biomass (seaweed) could be a valuable bioresource for heavy metal remediation from various water bodies.

A sensitive voltammetric sensor has been developed for hazardous methyl parathion detection (MP) using graphene oxide@Ce-doped TiO

The concentrations level and distribution of 16 US EPA polycyclic aromatic hydrocarbon (PAHs) from the water treatment plant (WTP), sewage treatment plant (STP), and industrial water treatment plant (ITP) sludge in Taiwan were determined and then assessed the sources, and potential toxicity (carcinogenic polycyclic aromatic hydrocarbons [CPAHs] and toxic BaP equivalent [TEQ]). Results indicated that the total concentrations of PAHs ranged between 58 and 16,436 μg/kg dw. Among the 17 samples, the 2-4 ring of total PAHs were the predominant compound in three kinds of treatment plant (> 60%). Especially, ITP1 owns 95.8% of 2-4 ring of total PAHs and ITP3 owns 54% of five- and six-ring of total PAHs. The molecular indices and principal component analysis (PCA) were used to determine the source contributions, with the results showing that the contributions of combustion/grass, coal or wood combustion and combustion/ liquid (oil) fossil fuel combustion. A PAH toxicity indicated by TEQ was 2.5-506 μg TEQ/g dw. Although, the results indicated that these were not recommended for land applications, but analyses are beneficial to develop effective management strategies for controlling PAH discharge in treatment plants and establishing strategies for its reuse in managing pollutants.

Growth in population and thereby increased industrialization to meet its requirement, has elevated significantly the demand for energy resources. Depletion of fossil fuel and environmental sustainability issues encouraged the exploration of alternative renewable eco-friendly fuel resources. Among major alternative fuels, bio-ethanol produced from lignocellulosic biomass is the most popular one. Lignocellulosic biomass is the most abundant renewable resource which is ubiquitous on our planet. All the plant biomass is lignocellulosic which is composed of cellulose, hemicellulose and lignin, intricately linked to each other. Filamentous fungi are known to secrete a plethora of biomass hydrolyzing enzymes. Mostly these enzymes are inducible, hence the fungi secrete them economically which causes challenges in their hyperproduction. Biomass’s complicated structure also throws challenges for which pre-treatments of biomass are necessary to make the biomass amorphous to be accessible for the enzymes to act on it. The enzymatic hydrolysis of biomass is the most sustainable way for fermentable sugar generation to convert into ethanol. To have sufficient ethanol concentration in the broth for efficient distillation, high solid loading >20% of biomass is desirable and is the crux of the whole technology. High solid loading offers several benefits including a high concentration of sugars in broth, low equipment sizing, saving cost on infrastructure, etc. Along with the benefits, several challenges also emerged simultaneously, like issues of mass transfer, low reaction rate due to water constrains in, high inhibitor concentration, non-productive binding of enzyme lignin, etc. This article will give an insight into the challenges for cellulase action on cellulosic biomass at a high solid loading of biomass and its probable solutions.

Waste activated sludge contaminated with high levels of 4-nonylphenol (4-NP) is a major environmental concern. We have synthesized lignin-based biochar (LGBC) for use as a carbocatalyst in calcium peroxide (CP)-mediated sewage sludge pretreatment. Treatment of sewage sludge with 3.1 × 10

Although the pollution of coral reefs by microplastics (MPs) is an environmental problem of global significance, the effects of MP concentration on scleractinian corals remain largely underexplored. Herein, we exposed a representative scleractinian coral (Goniopora columna) to different concentrations (5-300 mg L

Biochars derived from three species of algae was synthesized by impregnating the green algae Ulva Ohnoi, red algae Agardhiella subulata, and brown algae Sargassum hemiphyllum with ZnCl

Potential toxic chemicals, specifically, polycyclic aromatic hydrocarbons (PAHs), are major sediment contaminants. Herein, green seaweed (Ulva lactuca) was used as a feedstock and pyrolyzed at temperature in the range between 300 and 900 °C. The metal-free carbocatalyst (GSBC) for peroxymonosulfate (PMS) activation to degrade PAHs contaminated sediments was studied. The effects of GSBC‒PMS treatment on microbial community abundance was studied as well. The pyrolysis temperature of GSBC preparation affected the PMS activation performance. Results show that GSBC700 exhibited remarkable catalytic characteristics in PAHs degradation by effective activation of PMS. The results also demonstrated that the sulfate radical-carbon-driven advanced oxidation processes (SR-CAOP) reaction achieved 87% and apparent rate constant (k

Ethyl esters of omega-3 fatty acids are active pharmaceutical ingredients used for the reduction in triglycerides in the treatment of hyperlipidemia. Herein, an ultrasonic packed-bed bioreactor was developed for continuous production of docosahexaenoic acid (DHA) and eicosapentaenoic acid (EPA) ethyl esters from DHA+EPA concentrate and ethyl acetate (EA) using an immobilized lipase, Novozym® 435, as a biocatalyst. A three-level–two-factor central composite design combined with a response surface methodology (RSM) was employed to evaluate the packed-bed bioreactor with or without ultrasonication on the conversion of DHA + EPA ethyl ester. The highest conversion of 99% was achieved with ultrasonication at the condition of 1 mL min−1 flow rate and 100 mM DHA + EPA concentration. Our results also showed that the ultrasonic packed-bed bioreactor has a higher external mass transfer coefficient and a lower external substrate concentration on the surface of the immobilized enzyme. The effect of ultrasound was also demonstrated by a kinetic model in the batch reaction that the specificity constant (V′max/K2) in the ultrasonic bath was 8.9 times higher than that of the shaking bath, indicating the ultrasonication increased the affinity between enzymes and substrates and, therefore, increasing reaction rate. An experiment performed under the highest conversion conditions showed that the enzyme in the bioreactor remained stable at least for 5 days and maintained a 98% conversion.

This study focuses on the development of flat sheet thin film nanocomposite (TFN) pressure retarded osmosis (PRO) membranes for the enhancement of osmotic power generation by the incorporation of laboratory-synthesised graphene oxide (GO) into the polysulfone (PSf) polymer matrix. A series of membranes containing different weight percent of GO (0, 0.1, 0.25, 0.5 and 1.0 wt%) were fabricated via a phase inversion method with polyethylene glycol (PEG) as the pore forming agent. The results show that the TFN-0.25GO membrane has excellent water flux, salt reverse flux, high porosity and an enhanced microvoids morphology compared to the control membrane. The highest power density was achieved when TFN-0.25GO was used is 8.36 Wm&minus, 2 at pressure &gt, 15 bar. It was found that the incorporation of GO into the polymer matrix has significantly improved the intrinsic and mechanical properties of the membrane.

Recently, microalgal biomass has become an attractive and sustainable feedstock for renewable production of various biochemicals and biofuels. However, attaining required productivity remains a key challenge to develop industrial applications. Fortunately, mixotrophic cultivation strategy (MCS) is leading to higher productivity due to the metabolic ability of some microalgal strain to utilise both photosynthesis and organic carbon compared to phototrophic or heterotrophic processes. The potential of MCS is being explored by researchers for maximized biochemicals and biofuels production however it requires further development yet to reach commercialization stage. In this review, recent developments in the MCS bioprocess for selective value-added (carotenoids) products have been reviewed; synergistic mechanism of carbon and energy was conferred. Moreover, the metabolic regulation of microalgae under MCS for utilized carbon forms and carbon recycling was demonstrated; Additionally, the opportunities and challenges of large-scale MCS have been discussed.

This study aims to clarify the removal mechanism and to calculate the effective current of electrocoagulation (i.e., EC) for treating wastewater containing Ni(II), Cu(II), and Cr(VI). The adsorption behavior of various heavy metals onto Al(OH)3 coagulant generated by the EC process was investigated and the estimating method of the corresponding current was established. Results indicate that adsorption of single Ni(II) and Cu(II) by Al(OH)3 coagulant can be simulated by the Langmuir isotherm, while Cr(VI) adsorption fits the Freundlich isotherm better. As treating single heavy metal of wastewater, the removal mechanism of the EC process is the adsorption reaction. Under the coexisting condition, the Ni(II) and Cu(II) will compete for the same active sites on the Al(OH)3 surface and Cu(II) suppresses Ni(II) adsorption. As treating the coexisting heavy metals, Ni(II) removal not only associates with adsorption but also with the coprecipitation. In contrast, Cr(VI) does not compete with other metal ions for the same type of adsorption sites. Whether single or coexisting conditions, the adsorption capacity of heavy metals onto Al(OH)3 coagulants can be used to compute the necessary current to effectively remove heavy metals in the EC system.

Heterogeneous Fenton-like catalyst prepared by dispersing iron oxides in activated carbon (FeOx@AC) has frequently been assembled for advanced oxidation processes (AOPs). An intriguing but barely emphasized property of FeOx@AC is that it can be easily reactivated through a simple carbothermal reaction. Importantly, by this manner the life time of FeOx@AC could be effectively enhanced. We herein reported the synthesis of FeOx@ACs hydrothermally with assistance of several commercially available surfactants and their performance in degrading real dye wastewater were evaluated. In general, as-synthesized FeOx@ACs were noted to equip high Fe content. Deposited FeOx reduced the fraction of micropores but simultaneously introduced additional mesopores and macropores. Elevated magnetite content was observed in FeOx@AC equipped with high fraction of micropore and mesopore and macropore but fast dye degradation occurred at FeOx@AC possessing low fraction of micropore along with low mesopores and macropores. Reactivation via carbothermal reaction redistributed the deposited FeOx by increasing micropores while decreasing mesopores and macropores. Importantly, well dispersed FeOx synthesized with the assistance of surfactants exhibited high resistance to the corrosion in the degradation process. For the perspective of circular economy, deep understanding the material chemistry of FeOx@AC would be of particularly interest for further enhancing its life time.

Hierarchical porous birnessite-MnO2-based nanostructure composite materials were prepared on a nickel foam substrate by a successive ionic layer adsorption and reaction method (SILAR). Following composition with reduced graphene oxide (rGO) and multiwall carbon nanotubes (MWCNTs), the as-obtained MnO2, MnO2/rGO and MnO2/rGO-MWCNT materials exhibited pore size distributions of 2&ndash, 8 nm, 5&ndash, 15 nm and 2&ndash, 75 nm, respectively. For the MnO2/rGO-MWCNT material in particular, the addition of MWCNT and rGO enhanced the superb distribution of micropores, mesopores and macropores and greatly improved the electrochemical performance. The as-obtained MnO2/rGO-MWCNT/NF electrode showed a specific capacitance that reached as high as 416 F&middot, g&minus, 1 at 1 A&middot, 1 in 1 M Na2SO4 aqueous electrolyte and also an excellent rate capability and high cycling stability, with a capacitance retention of 85.6% after 10,000 cycles. Electrochemical impedance spectroscopy (EIS) analyses showed a low resistance charge transfer resistance for the as-prepared MnO2/rGO-MWCNT/NF nanostructures. Therefore, MnO2/rGO-MWCNT/NF composites were successfully synthesized and displayed enhanced electrochemical performance as potential electrode materials for supercapacitors.

A series of experiments with different NaCl concentrations added to the PCB (printed circuit board) wastewater were prepared to investigate the chloride effect on the formation of aluminum floc and removal efficiency of Cu and Ni. The effects of pH, current density, and different concentration of NaCl were studied and the results are discussed. Results imply that chloride ions are favored to avoid the passivation of the aluminum anode in the EC (electro-coagulation) system. Chloride ions used as the electrolyte can facilitate the release of Al3+, which results in the current efficiency of over 100% in the EC system. For the PCB factory&rsquo, s wastewater, the EC system could remove Cu2+ and Ni2+ effectively (both Cu and Ni concentration of treated wastewater was less than 1.0 mg/L within three minutes). PCB wastewater&rsquo, s pH value could maintain stably about 9.0 in the EC system when the initial pH value was around 2.5. The estimated electricity consumption for treating PCB wastewater by the EC process was about 0.894 kWh for each meter of cubic wastewater.

Dyes are hazardous compounds commonly found in industrial wastewaters. Efficient and inexpensive removal of dye molecules from the water matrix has been demonstrated by adsorption processes. Magnetic nano-adsorbents, such as metal ferrites, can be efficiently recovered from the reaction mixture after treating the pollutant. Herein, MFe2O4@GO (M = Cu, Co or Ni) was synthesized via solution combustion method for the removal of dye molecules from aqueous solutions. The characteristics of the MFe2O4@GO, including surface area and pore diameter, surface functional groups, and elemental composition, were examined. Methylene blue was used as representative dye pollutant. Batch adsorption results conformed to the Langmuir isotherm. Maximum adsorption capacities of the MFe2O4@GO (M = Cu, Co or Ni) were 25.81, 50.15 and 76.34 mg g−1, respectively. Kinetics of methylene blue adsorption fitted the pseudo-second-order model. Overall, NiFe2O4@GO exhibited the highest adsorbent performance among the graphene-metal ferrites investigated, primarily because of its high specific surface area and presence of mesopores.

A direct and efficient hydrothermal system has been established for the synthesis of MoS

A facile impregnation method was used to fabricate a hybrid CoO-3D ordered mesoporous carbon nitride (CoO@mpgCN) catalyst that effectively activated peroxymonosulfate (PMS) for the degradation of pharmaceutical chemical, exemplified by antibiotic sulfamethoxazole (SMX) in aqueous solutions. The CoO@mpgCN/PMS system exhibited high catalytic reactivity and SMX removal efficiency over a wide pH range with an observed rate constant (kobs) of 0.314 min−1. Furthermore, CoO@mpgCN was stable with consistently high degree of SMX degradation without having cobalt dissolution and loss of catalytic activity for at least five consecutive cycles. The significant catalysis performance of CoO@mpgCN was due to its uniformly distributed mesopores, large specific surface area, and high electron transfer ability at the active CoO sites. Both quenching experiments and electron paramagnetic resonance (EPR) analysis verified the yield, in abundance, of highly active species, specifically SO4 − and OH from the CoO@mpgCN activation of PMS, primarily. Hence, SMX degradation followed a radical chain reaction mechanism. The result of this study revealed a novel prospective of CoO@mpgCN composite as PMS activator for the remediation of recalcitrant pollutants in water.

Sludge from a groundwater treatment plant was used to prepare biochar by pyrolysis. The Fe–Mn rich biochar was used to activate percarbonate for the remediation of polycyclic aromatic hydrocarbons (PAHs) contaminated aquatic sediments. Results showed that the sludge–derived biochar (SBC) produced at a pyrolysis temperature of 700 °C was the most effective in activating percarbonate, which exhibited significant oxidative removal of PAHs. PAHs degradation took place via a Fenton-like oxidation manners, contributed from the Fe3+/Fe2+ and Mn3+/Mn2+ redox pairs, and achieved the highest degradation efficiency of 87% at pH0 6.0. Reactions between oxygenated functional groups of biochar and H2O2 generated of O2•– and HO• radicals in abundance under neutral and alkaline pH was responsible for the catalytic degradation of PAHs. Our results provided new insights into the environmental applications of SBC for the green sustainable remediation of organics-contaminated sediments and aided in reduction of associated environmental and health risk.

In this work, nano V/TiO2 catalysts at different molar ratios were prepared and fabricated as the electrocatalytic electrodes for electrocatalytic degradation. The effect of the vanadium doping on the surface morphology, microstructural, and specific surface area of V/TiO2 catalysts was probed by field emission scanning electron microscope (FESEM) x-ray diffractometer (XRD), and Brunauer&ndash, Emmett&ndash, Teller (BET), respectively. Afterward, the solution of Acid Red 27 (AR 27, one kind of azo dye) was treated by an electrocatalytic system in which the nano V/TiO2 electrode was employed as the anode and graphite as the cathode. Results demonstrate that AR 27 can be effectively degraded by the nano V/TiO2 electrodes, the highest removal efficiency of color and total organic carbon (TOC) reached 99% and 76%, respectively, under 0.10 VT (molar ratio of vanadium to titanium) condition. The nano V/TiO2 electrode with high specific surface area facilitated the electrocatalytic degradation. The current density of 25 mA cm&minus, 2 was found to be the optimum operation for this electrocatalytic system whereas the oxygen was increased with the current density. The electricity consumption of pure TiO2 and nano V/TiO2 electrode in this electrocatalytic system was around 0.11 kWh L&minus, 1 and 0.02 kWh L&minus, 1, respectively. This implies that the nano V/TiO2 electrode possesses both high degradation and energy saving features. Moreover, the nono V/TiO2 electrode shows its possible repeated utilization.

Contamination by microplastics (MPs) and the associated organic pollutants has caused potential threats to the ecological environment of global waters. In this study, MPs were sampled by trawling from the surface waters of the estuary, fishing port entrance and harbor entrance areas connected to the southwestern coast of Taiwan. Moreover, the abundance, morphological characteristics, composition, and associated polycyclic aromatic hydrocarbons (PAHs) of MPs were analyzed. The abundance of MPs was 0.36 ± 0.21 items/m3, which was 6.4 ± 10.7% of the abundance of zooplanktons. The average abundance of MPs was the highest in the estuary area, indicating that river transport was the primary way for MPs to enter the ocean. The most dominant MPs were small (0.33–2 mm; 78.8 ± 8.1%), colored (60.0 ± 12.8%), fragments (66.1 ± 10.6%), comprising PE (52.6 ± 7.6%), and PP (38.7 ± 9.4%). The decomposition of various plastic products and disposable plastic packaging may be the most significant source. The total concentration of PAHs in MPs ranged from 104 to 3595 ng/g dw, with an average of 818 ± 874 ng/g dw. The diagnostic ratios and the results of principal component analysis (PCA) and multiple linear regression of the absolute principal component scores (MLR-APCS) indicated that the PAHs were mainly contributed from sources related to petrogenic (71.4%) and vehicles (28.6%). Most likely due to MPs on the sea surface coming into contact with floating oil spills from ships or floating tar particles.

Shellfishes can easily accumulate metals via water and sediment and which may pose a human health risk by consumption. This study assessed the distribution of metals, including Cd, Cr, Cu, Pb, Ni, Zn, and Hg, in soft tissues of hard clam (Meretrix lusoria), surrounding water body, and sediment in the southwest coast of Taiwan. Hard clams contained the relatively higher concentration of the essential element, such as Zn, Cu, and Ni, and the metal concentration from high to low was Zn > Cu > Ni > Cd > Cr > Pb > Hg. However, the metal concentrations found in hard clam all were lower than the Sanitation Standard for Aquatic Animal of Taiwan. Results of bioaccumulation factors indicated that hard clam shows the ability of metal accumulation from water was higher than that from sediment. Moreover, the metal concentrations in hard clam were negatively correlated with body size except for Hg, which could be presented by the significant power function. Generally, hard clams from the aquaculture pond located on the southwest coast of Taiwan would not be harmful to adult consumers, except for people that consume shellfish more than 100 g. Besides strengthening the management of seafood safety and aquaculture, adjusting the eating and purchasing habits of the consumer could be a practical and feasible way for decreasing health risks. These results can assist the government in determining seafood safety and its implementation in Taiwan.

4-Nonylphenol (4-NP), a phenolic endocrine disruptor chemical (EDC), is known to have high toxicity to aquatic organisms and humans. The remediation of 4-NP-contaminated marine sediments was studied using red algae-based biochar (RAB) thermochemically synthesized from Agardhiella subulata with simple pyrolysis process under different temperatures of 300–900 °C in CO2 atmosphere. The RAB was characterized by XRD, Raman, FTIR spectroscopy, and zeta potential measurements. The calcium in RAB efficiently activated sodium percarbonate (SPC) to generate reactive radicals for the catalytic degradation of 4-NP at pH 9.0. The oxygen-containing functional groups reacted with H2O2, which increased the generation of reactive radicals under alkaline pH condition. Ca2+ ion was the active species responsible for 4-NP degradation. CaO/CaCO3 on RAB surface enhanced direct electron transfer, increased HO production, and 4-NP degradation in marine sediments. Langmuir‒Hinshelwood type kinetics well described the 4-NP degradation process. Remediation of contaminated sediments using RAB could be a sustainable approach toward closed-loop biomass cycling in the degradation of 4-NP contaminants.

Nanocomposite materials can enhance the capabilities of water treatment processes such as photocatalysis. In this work, novel light-driven nanocatalysts were synthesized by using nickel ferrite (NiFe

Producción Científica, Relevance of Biotechnology for a sustainable living has increased over the past few decades by addressing the different domains including agriculture, food, health care, livestock management, energy, environment, climate change, waste management and a multitude of other areas. Today, the subject not only encompasses life sciences and engineering, but spans across most of the human activities, affecting and influencing every one. The subject is poised to tackle emerging challenges like rapidly spreading global pandemics by providing solutions in the form of vaccines or drugs, immune boosters and diagnostics. Green processes, renewable clean energy, super foods and nutraceuticals, biodegradable polymers and materials are but a few of the outcomes of development in this field. In wake of the rapid deterioration of land and water resources and environment catalysed by anthropogenic activities, urgent calls have to be made on addressing the issues of solid, liquid and chemical waste management, atmospheric pollution, and moving towards greener manufacturing processes and deriving energy through renewable routes for a sustainable development and improved quality of life. It may not be incorrect to say that the world needs to move towards a sustainable bio-economy for human race to persist on this planet.

Lignin is the 3rd most abundant biopolymer surpassed by cellulose and hemicellulose and is the most abundant aromatics resource available on earth for utilization by mankind. It was considered undesirable historically which was usually burned as inefficient fuel. Lignin’s 3D recalcitrant nature caused hinderance to feasible biorefinery of holocellulosic fraction of biomass; however, with the rise of lignin biorefinery the concept has changed completely. Now modern biorefinery of biomass insists on making complete value of all the streams including lignin by valorising into variety of phenolics, biopolymers and other high value-added chemicals. Biological depolymerisation of lignin via enzymes is environmentally benign and preferred approach by virtue of low chemical requirement and disposal and energy demand; however, economic challenges are ahead. Robust enzymes are available in nature which can either modify or depolymerise lignin to add further value. Lignin modifying as well as lignin degrading auxiliary enzymes are instrumental and pave the way to a green process for lignin valorisation. This review article is focussed on various lignin degrading as well as lignin modifying enzymes produced by microorganisms especially fungi for degradation or modification of lignin, and its mechanisms, along with the strength and challenges for sustainable bio-based economy development.