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Macroalgae (seaweeds) are abundant in functional polysaccharides known for their unique biochemical activities. In this study, the antioxidant, anti-lipogenic, and anti-inflammatory activities of the fucoidan extracted from brown seaweed Sargassum siliquosum were investigated by 1,1-diphenyl-2-picrylhydrazyl (DPPH)-scavenging ability, lipid synthesis inhibition, and suppression of pro-inflammatory cytokine tumor necrosis factor-alpha (TNF-α) production, respectively. To examine the effect of molecular mass on fucoidan's bioactivities above, the extracted fucoidan was subject to hydrogen peroxide-mediated partial hydrolysis to obtain lower molecular mass compounds within the range of 107.3–3.2 kDa. Results indicated that fucoidan's antioxidant activity increased with a corresponding decrease in molecular mass; the dosage for the half-maximal response (EC50) dropped from 2.58 to 1.82 mg/mL when the molecular mass decreased from 107.3 to 3.2 kDa. In addition, both the anti-lipogenesis and anti-inflammatory activities of fucoidan were significantly enhanced by 71.1% and 36.7%, respectively, when the molecular mass decreased to about 3 kDa. To further test the effect of sulfation on fucoidan's bioactivities, low molecular mass fucoidan was treated with SO3-DMF to increase the sulfate content. The results indicated that when sulfate content increased from 18.7% to 32.1%, EC50 of DPPH decreased from 1.82 mg/mL to 0.86 mg/mL and the anti-inflammatory activity also increased by 35.2%; however, the anti-lipogenesis activity decreased.

A new electrode was constructed via the anodic electropolymerization of poly-(L-serine) (PLS) on an rGO-Nafion-modified glassy carbon electrode (GCE) for the detection of the emerging organic contaminant naproxen (NPX). The morphology, crystal phase, and surface elements of the electrode were investigated with SEM, TEM, XRD, Raman, ATR-FTIR, zeta potential, C-H-O, and XPS analyses. Results of the surface analysis showed a porous structure resembling graphene sheets inside the Nafion/GCE architecture. Various electrochemical parameters, including scan rate, pH, and NPX concentration, were studied to evaluate the performance of the electrode. The synergistic effect of PLS and rGO-Nafion greatly facilitated the catalytic oxidation of NPX on PLS/rGO-Nafion/GCE. Electrochemical NPX oxidation was a one-electron transfer and adsorption limited process. The optimal working potential was 0.92 V vs. Ag/AgCl. The oxidation current of NPX increased with the increase in the concentration of analyte and scan rate but decreased with pH. The modified electrode exhibited excellent linearity with respect to NPX concentration in the range of 4.3 to 87 μM and limit of detection of 0.23 μM (S/N = 3). The PLS/rGO-Nafion/GCE is a fast, sensitive, reliable, and economical electrode for the detection of NPX in water.

An effective improvement of hydrogen evolution from water splitting under solar light irradiation was investigated using quantum dots (QDs) compounds loaded onto a Au/TiO2 photocatalyst. First, Au/TiO2 was prepared by the deposition-precipitation method, and then sulfide QDs were loaded onto the as-prepared Au/TiO2 by a hydrothermal method. QDs were loaded onto Au/TiO2 to enhance the energy capture of visible light and near-infrared light of the solar spectrum. The results indicated that the as-prepared heterojunction photocatalysts absorbed the energy from the range of ultraviolet light to the near-infrared light region and effectively reduced the electron-hole pair recombination during the photocatalytic reaction. Using a hydrothermal temperature of 120 °C, the as-prepared (ZnS–PbS)/Au/TiO2 photocatalyst had a PbS QDs particle size of 5 nm, exhibited an energy gap of 0.92 eV, and demonstrated the best hydrogen production rate. Additionally, after adding 20 wt % methanol as a sacrificial reagent to photocatalyze for 5 h, the hydrogen production rate reached 5011 μmol g−1 h−1.

Bromide elevation in surface freshwater is unavoidable due to climate change and anthropogenic activities. Freshwater impaired by algal activity and bromide elevation has become problematic worldwi...

Tap water contains some heavy metals and bio-organic substances with variety of concentration and these cannot be treated using regular physicochemical processes. So the present study, aims at evaluating the effectiveness of the sterilization using electrocatalytic technique with Escherichia coli (E. coli) as the observed index. The operational parameters such as anode material, voltage, inflow method, and electrode number are studied to understand the variation of pH, conductivity, E. coli, and residual chlorine of tap water. The outcome reveals that the maximum sterilization efficiency of E. coli is obtained using the titanium dioxide electrode, followed by ruthenium dioxide and graphite. A disinfection efficiency of 98% can be easily achieved. Also, the appropriate increase in the operating voltage can increase the sterilization efficiency and decrease the treatment time. The sterilization efficiency of the E. coli can reach 100% under the continuous inflow of tap water and the voltage of 60 V for 1 min, which meets the conventional standard of drinking water (6 CFU/100ml). The estimated operating cost of treatment of 1 ton of tap water is NTD 1.7.

Bacterial cellulose (BC) is higher in demand due to its excellent properties which is attributed to its purity and nano size. Komagataeibacter xylinum is a model organism where BC production has been studied in detail because of its higher cellulose production capacity. BC production mechanism shows involvement of a series of sequential reactions with enzymes for biosynthesis of cellulose. It is necessary to know the mechanism to understand the involvement of regulatory proteins which could be the probable targets for genetic modification to enhance or regulate yield of BC and to alter BC properties as well. For the industrial production of BC, controlled synthesis is desired so as to save energy, hence genetic manipulation opens up avenues for upregulating or controlling the cellulose synthesis in the bacterium by targeting genes involved in cellulose biosynthesis. In this review article genetic modification has been presented as a tool to introduce desired changes at genetic level resulting in improved yield or properties. There has been a lack of studies on genetic modification for BC production due to limited availability of information on whole genome and genetic toolkits; however, in last few years, the number of studies has been increased on this aspect as whole genome sequencing of several Komagataeibacter strains are being done. In this review article, we have presented the mechanisms and the targets for genetic modifications in order to achieve desired changes in the BC production titer as well as its characteristics.

In this study, the preparation procedures for the polysulfone (PSf) substrate and polyamide (PA) selective layers were systematically investigated to determine their effects on the separation performance of thin-film composite (TFC) forward osmosis (FO) membranes in terms of the permeate flux (Jw) and reverse solute flux (Js). Furthermore, the PA active layer was modified by adding different proportions of an emerging material, graphene oxide (GO), to increase Jw and decrease Js. The experimental results indicated that special attention should be paid to the preparation of the PSf casting solution, which required thorough degassing, sealing, and humidity and temperature control. The optimum casting height was discovered to be 175 μm. For PA layer formation, the same amount of polymer solutions (resulting thickness of 78.5 μm) on the top surface of the PSf substrate (on the side facing the water during phase inversion) resulted in the highest FO performance. GO modification of the PA layer at the dosage of 0.0175 wt% considerably enhanced Jw to 14 L m−2 h−1 and reduced Js to 0.23 mol m−2 h−1. However, higher GO dosage (0.02 wt%) led to lower membrane performance due to aggregation of GO nanoparticles, as confirmed using scanning electron microscopy. Next, the prepared membranes were applied to dye rejection and sludge concentration for water recovery. The virgin and modified FO membranes both exhibited high rejection efficiency (≥96.0 %) for dyes commonly used in the textile industry. The 0.0175 %-GO-modified FO membrane exhibited a higher concentration factor (1.67) and greater water recovery (40.0 %) than the virgin membrane (1.45 and 31.2 %, respectively). Therefore, the application of FO for water recovery is economic and environmentally friendly in terms of saving the transportation cost of sludge disposal while recovering water for reuse in wastewater treatment plants.

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 (NiFe2O4) to nanoenable graphene oxide (GO) substrates. GO is an emerging 2D nanomaterial with high conductivity and adsorption properties. Moreover, the electric properties of GO improve photocatalytic performance by promoting charge carrier separation. Results of the characterization of the nickel ferrite nanoenabled graphene oxide (NiFe2O4@GO) nanocomposites demonstrate that homogeneous and stable photocatalysts were produced. The as-synthesized nanocatalysts enabled complete decolorization of the colored water matrix in short irradiation times of 150 min using minimal catalyst loading at 0.5 g L−1. The selective hook and destroy mechanism reduced the competitive effect of co-existing ions in solution. Furthermore, the use of specific scavengers helped to elucidate the degradation mechanisms of organic dye methylene blue by NiFe2O4@GO nanocomposites.

This study proposed a method for analysis of 10 phthalate esters compounds from wastewater treatment plant sludges. The analytical efficiency of GC-MS for of target compounds was verified by a standard mixture of phthalate esters. The response factors related to the respective internal standards from a five-point calibration curve quantified the phthalate esters in individual compounds. Based on the literature compiled by environmental agencies, new generation phthalate compounds have been developed, such as di-iso-nonyl phthalate (DiNP), di-iso-decyl phthalate (DiDP), as alternative to conventional phthalates. The analytical results showed that the total PAEs concentration was in the range from 7.4 to 138.6 mg kg

In this study, Fenton oxidation and activated persulfate oxidation were used to investigate the optimized in situ chemical oxidation (ISCO) process for its efficiency on petroleum-hydrocarbon contaminated groundwater cleanup. In the batch and column experiments using benzene and toluene as the target compounds, oxidant depletion, soil oxidant demand (SOD), adsorption of oxidant on soils, and oxidation kinetics were studied. Results show that Fenton oxidation process was more catalytic than activated persulfate oxidation by ferrous iron catalysis. Higher SOD value was obtained for H2O2 than persulfate because H2O2 had higher reactivity to soil organic matter. In addition, increased benzene and toluene oxidation rates were observed with increased concentrations of H2O2 and persulfate oxidants. The calculated pseudo first-order decay rate constants (k’) for Fenton and activated persulfate oxidation processes were 1.65 and 0.13 1/h for benzene and 1.28 and 0.1 1/h for toluene, respectively. Compared to persulfate oxidation, results indicate that Fenton oxidation had much higher reaction rates on petroleum hydrocarbon oxidation. Results from the column experiment show that up to 5.94 pore volumes (PVs) of H2O2 solution and 12.85 PVs of persulfate solution were required to cleanup benzene and toluene contaminated groundwater with an oxidant concentration of 10 wt%, ferrous iron concentration of 100 mg/L, and initial contaminant concentration of 50 mg/L. Results indicate that the Fenton oxidation process would be a more practical and efficient approach to remediate petroleum-hydrocarbon contaminated groundwater. The results would be useful in developing an ISCO system for a practical field application to cleanup benzene and toluene contaminated groundwater.

Microbial fermentation is the source of commercial lactic acid (LA), and the price of fermentation-derived LA is heavily challenged by the feedstock price. This study evaluated four different categ...

Fungal delignification can be a feasible process to pretreat biomass for bioethanol production if its performance is improved in terms of efficiency through a few modifications. The aim of this study was to enhance the biodelignification pretreatment of rice straw using laccase in the presence of ionic liquid (1-Allyl-3-methylimidazolium chloride, [AMIM]Cl) or surfactant (TritonX-100). Addition of 750 mg/L [AMIM]Cl and 500 mg/L TritonX-100 increases the lignin removal to 18.49% and 31.79%, which is higher than that of laccase only (11.97%). The enzymatic saccharification process was carried out based on different strategies. The highest cellulose conversion, 40.96%, 38.24%, and 37.91%, was obtained after 72 h of enzymatic saccharification when the substrate was washed with distilled water after pretreatment of rice straw with laccase + TritonX-100, laccase + [AMIM]Cl, and laccase only, respectively. In addition, the morphology and structure changes of pretreated and untreated rice straw were studied. Both surface area and cellulose crystallinity are substantially altered after laccase + [AMIM]Cl and laccase + TritonX-100 pretreatment. Enhanced saccharification efficiency of rice straw was achieved by laccase pretreatment with ionic liquid or surfactant in a single system.

Bacterial cellulose (BC) represents a novel bio-origin nonomaterial with its unique properties having diverse applications. Increased market demand and low yield are the major reason for its higher cost. Bacteria belonging to Komagataeibacter sp are the most exploited ones for BC production. Development of a cost-effective bioprocess for higher BC production is desirable. Though static fermentation modes have been majorly employed for BC production using tray fermenters, agitated mode has also been employed successfully with air-lift fermenters as well as stirred tank reactors. Bioprocess advances in recent years has led BC production to an upper level; however, challenges of aeration requirement and labor cost towards the higher end is associated with static cultivation at large scale. We have discussed the bioprocess development for BC production in recent years along with the challenges associated and the path forward.

The nonstructural antigen protein 3 of the hepatitis C virus (HCV NS3), commonly-used for HCV ELISA diagnosis, possesses protease and helicase activities. To prevent auto-degradation, a truncated NS3 protein was designed by removing the protease domain. Firstly, it was overexpressed in E. coli by IPTG induction under two different temperatures (25 and 37 °C), and purified using affinity chromatography to attain homogeneity above 90%. The molecular mass of purified protein was determined to be approx. 55 kDa. While lowering the temperature from 37 to 25 °C, the yield of the soluble fraction of HCV NS3 was increased from 4.15 to 11.1 mgL−1 culture, which also improved the antigenic activity and specificity. The protein stability was investigated after long-term storage (for 6 months at −20 °C) revealed no loss of activity, specificity, or antigenic efficacy. A thermal stability study on both freshly produced and stored HCV NS3 fractions at both temperatures showed that the unfolding curve profile properly obey the three-state unfolding mechanism. In the first transition phase, the midpoints of the thermal denaturation of fresh NS3 produced at 37 °C and 25 °C, and that produced after long-term storage at 37 °C and 25 °C, were 59.7 °C, 59.1 °C, 55.5 °C, and 57.8 °C, respectively. Microplates coated with the fresh NS3 produced at 25 °C or at 37 °C that were used for the HCV ELISA test and the diagnosis outcome were compared with two commercial kits—Abbott HCV EIA 2.0 and Ortho HCV EIA 3.0. Results indicated that the specificity of the HCV NS3 produced fresh at 25 °C was higher than that of the fresh one at 37 °C, hence showing potential for application in HCV ELISA diagnosis.

Fish bones (FBs) are aquatic by-products that are sources of antioxidant-active peptides, calcium dietary supplements, and biomedical materials. Usually, fermentation of these by-products via microorganisms brings desirable changes, enhancing their value. This study investigates the value addition of FB when fermented with Monascus purpureus (MP) for different time intervals, such as 3 days (F3) and 6 days (F6). The results indicate that the soluble protein, peptide, amino acid and total phenol content, as well as the antioxidant capacity (DPPH, ABTS+ radical scavenging activity, and relative reducing power), of F3 and F6 were significantly increased after fermentation. Furthermore, the ROS contents of F3 and F6 were reduced to a greater extent than that of hydrogen peroxide (H2O2) in Clone-9 cells. The MMP integrity, as well as the SOD, CAT, and GPx activity, of F3 and F6 were also increased significantly compared to the H2O2 in Clone-9 cells. Notably, F3 and F6 displayed significant reductions in ROS content, as well as elevate, SOD activity and MMP integrity in Clone-9 cells, when compared with the native FB. These results indicate that the FBs fermented with MP for 3 days (F3), and 6 days (F6) have antioxidant capacity, with possible applications as natural food supplements.

The need to develop sustainable alternatives for pretreatment and hydrolysis of lignocellulosic biomass (LCB) is a massive concern in the industrial sector today. Breaking down of LCB yields sugars and fuel in the bulk scale. If explored under nanotechnology, LCB can be refined to yield high-performance fuel sources. The toxicity and cost of conventional methods can be reduced by applying nanoparticles (NPs) in refining LCB. Immobilization of enzymes onto NPs or used in conjugation with nanomaterials would instill specific and eco-friendly options for hydrolyzing LCB. Nanomaterials increase the proficiency, reusability, and stability of enzymes. Notably, magnetic NPs have bagged their place in the downstream processing of LCB effluents due to their efficient separation and cost-effectiveness. The current review highlights the role of nanotechnology and its particles in refining LCB into various commercial precursors and value-added products. The relationship between nanotechnology and LCB refinery is portrayed effectively in the present study.

In this study, biochar derived from spent coffee grounds (SCGB) was used to adsorb norfloxacin (NOR) in water. The biochar properties were interpreted by analysis of the specific surface area, morphology, structure, thermal stability, and functional groups. The impacts of pH, NOR, and ion's present on SCGB performance were examined. The NOR adsorption mode of SCGB is best suited to the Langmuir model (R2 = 0.974) with maximum absorption capacity (69.8 mg g−1). By using a Response Surface Method (RSM), optimal adsorption was also found at pH of 6.26, NOR of 24.69 mg L−1, and SCGB of 1.32 g L−1. Compared with biochars derived from agriculture such as corn stalks, willow branches, potato stem, reed stalks, cauliflower roots, wheat straw, the NOR adsorption capacity of SCGB was 2–30 times higher, but less than 3–4 times for biochars made from Salix mongolica, luffa sponge and polydopamine microspheres. These findings reveal that spent coffee grounds biochar could effectively remove NOR from aqueous solutions. Approaching biochar derived from coffee grounds would be a promising eco-friendly solution because it utilizes solid waste, saves costs, and creates adsorbents to deal with emerging pollutants like antibiotics.

Malachite green (MG) is used as fungicide/parasiticide in aquaculture, its persistence is detrimental as it exhibits carcinogenic effects to aquatic organisms. Bacterial laccase evaluated as the best enzyme at extreme condition for aquatic MG removal. Study aims to increase laccase concentration, CotA-laccase from Bacillus subtilis was cloned and overexpressed in Escherichia coli. Optimal catalysis for purified CotA-laccase were at pH 5.0, 60 °C, and 1 mM of (2,2-azino-di-[3-ethylbenzothiazoline-sulphonate-(6)]) with Km and Kcat 0.087 mM and 37.64 S-1 respectively. MG biodegradation by CotA-laccase in clam and tilapia pond wastewaters and cytotoxic effect of biodegraded products in grouper fin-1 cells were determined. MG degradation by CotA-laccase was equally efficient, exhibiting upto 90–94% decolorization at freshwater and saline conditions and treated solution was non-toxic to GF-1 cells. Thus, recombinant-CotA-laccase could be an environmentally-friendly enzyme for aquaculture to remove MG, thereby effective to reduce its accumulation in aquatic organisms and ensuring safe aquaculture products.

Methylmercury (MeHg) presents high toxicity to humans and can be accumulated to organisms via the food chains. In aquatic environments, MeHg is mainly formed by microorganism using the bioavailable inorganic mercury in sediment. In this study, a total of 120 surface sediments from 20 sites in the Kaohsiung Harbor were collected quarterly in the period from July 2016 to October 2017 and analyzed for total mercury (THg), bioavailable inorganic mercury (BIHg), MeHg, and several geochemical parameters. The concentrations of THg, BIHg, and MeHg in sediment were 455-5108, 7.0-1021, and 0.84-24.1 μg/kg dw, respectively. Results indicated that the percentage of MeHg to THg (MeHg ratio) in most sediment (85%) is1.2%. Correlation analysis showed that MeHg in sediment was mainly controlled by BIHg (r = 0.759, p 0.01), while the concentration of BIHg in sediment was mainly related to TOC (r = 0. 480, p 0.01) and THg (r = 0.435, p 0.01). The relationship between total bioavailable inorganic mercury (containing BIHg and the bioavailable inorganic mercury used in the synthesis of MeHg) and MeHg concentration in the sediments that collected from the estuary, harbor channel, and the entrance was established by a Michaelis-Menten model to predict the maximum value of MeHg. The efficiency of Hg methylation in the sediments of Kaohsiung Harbor is significantly affected by the total bioavailable inorganic mercury and the related environmental factors. In addition, changes in environmental conditions caused by local seasonality should also be an important factor to consider when assessing the efficiency of Hg methylation.

The main objective of this study was to evaluate the effect of different pyrolysis temperatures on the formation of polycyclic aromatic hydrocarbons (PAHs) in biochar originated spent coffee ground (SCG) and the tetracycline (TC) adsorption behavior of biochar in water. The results showed that biochar synthesized at 500 °C (SCG 500) contained low PAHs (600 µg kg−1) and the highest TC adsorption efficiency. In addition, the characteristics, influencing factors on TC adsorption, and the related mechanisms of SCG 500 were comprehensively investigated. The results showed that the highest efficiency was observed at pH of 7 and the presence of ions in salinity solution reduced the adsorption capacity of SCG 500. The electrostatic interaction, hydrogen bonding, and π-EDA were the major adsorption mechanisms. Safety PAHs level, low-cost, widely material sources and high TC removal capacity suggested that SCG 500 was a promising environmentally friendly effective absorbent.

An electrode made of loofah sponge derived activated carbon supported on nickel foam (AC/Ni) was successfully fabricated and used to remove ammonium ion (NH4+) from aqueous solution. A multilayer adsorption isotherm was used to describe ammonium electro-sorption on AC/Ni electrodes at different temperature, initial NH4+ concentration, and electrical field. The cyclic voltammetry (CV) results suggested that the electrical capacitance of AC/Ni electrodes, with the AC being prepared without preheating (OAC) or with low temperature heating (i.e., 300 AC), were higher than those prepared at high preheating temperature (i.e., 400 AC and 500 AC). Increasing the electro-sorption temperature from 10 to 50 °C decreased the monolayer NH4+ adsorption capacity from 5 to ca. 2–3 mg-N g−1, respectively. Background electrolyte, namely, sodium sulfate, exhibited significant competitive effect on the adsorption of ammonium ion at sodium ion concentration > 10−2 M. The activation energy and heat of adsorption were 9–23.2 kJ mol−1 and −3.7–−10.7 kJ mol−1, respectively, indicating a physisorption and exothermic adsorption characteristics. Based on the kinetics and thermodynamics analysis, there was slight increase in the activation energy with elevating preheating temperature, which increased the quantity of micro-pores and surface heterogeneity of the AC materials. Overall, results clearly demonstrated that carbon pyrolysis played a role on the capacitive charging behaviors of electrodes and the efficiency of NH4+ electro-sorption on the AC/Ni electrodes.

A simple and facile synthesis method is developed for the fabrication of CoO loaded ordered mesoporous carbon nitride (CoO@meso-CN) composites, at various CoO loadings, and used, for the first time, to activate persulfate (PS) for methylene blue (MB) degradation. The interfacial interaction between the ultrafine CoO nanoparticles, immobilized by high surface area, regular mesopores, and graphitic nature of the meso-CN support can further enhance the catalytic activation of PS for methylene blue (MB) degradation. Among all catalysts studied, the 5-wt% CoO@meso-CN exhibits the best catalytic performance with a kobs of 0.264 min−1. High initial pH, especially at pH-11, is more beneficial for PS activation. Furthermore, the CoO@meso-CN nanocatalyst is highly stable with a consistently high degree of MB degradation and negligible cobalt leaching for at least 5 consecutive catalytic cycles. Both SO4 − and OH are the major reactive species based on results of EPR and quenching experiments. The degradation intermediates of MB are also identified by HPLC/MS/MS and the possible degradation pathway is proposed. Results clearly demonstrate that CoO@meso-CN is a promising green catalyst with enormous potential for the remediation of hazardous chemicals using PS.

In this study, an environmentally friendly and economically viable bamboo biochar (BB) was modified by Fe3O4 and was applied for the treatment of real river sediments containing the endocrine disruptor chemical (EDC) 4-nonylphenol (4-NP). The microporosity of Fe3O4–BB was clearly observed from the N2 adsorption isotherms. The catalytic performance of Fe3O4–BB is highly dependent on pH and the catalyst dosage. The degradation efficiency of 4-NP (85%) was achieved at pH 3.0 using an initial dosage of 3.33 g L−1 Fe3O4–BB and 2.3 × 10−5 M persulfate (PS) in a biochar–sediment system. The kinetic behavior of 4-NP degradation with catalysis can be accounted by using the Langmuir-Hinshelwood type kinetic model. The MTT assay results indicated that Fe3O4–BB has a low potent cytotoxic effect and is therefore suitable for application in remediation of contaminated sediment.

The advanced oxidation process (AOP) is a promising remediation technology for persistent organic pollutants in the environment. We herein investigated the ability of a magnetic carbon microsphere (CM)-based composite catalyst (Fe3O4−CM) to catalyze sodium persulfate (Na2S2O8, SPS) for the remediation of marine sediments contaminated with polycyclic aromatic hydrocarbons (PAHs). The effectiveness of the process parameters, catalyst dose, and initial pH were investigated. Using the optimized conditions, 87% of the PAHs were removed in the Fe3O4−CM/PS system within 24 h, compared with 59% and 41% in the case of persulfate (PS) and CM/PS (PS concentration = 1.3 × 10−5 M, catalyst concentration = 5.0 g/L, pH = 6.0) alone. The PAH reduction rate can be attributed to the uniform graphitic structure of Fe3O4−CM, which serves as an effective matrix for PAH degradation by providing additional active sites. The degradation of the PAHs was related to the number of rings in their structure, as confirmed by the higher degradation efficiency observed for high aromatic ring PAHs (HPAHs). Thus, we herein demonstrated the CM-mediated electron transfer catalysis of the surface functional groups at circumneutral pH values in the Fe3O4−CM/PS system to the highly efficient removal of PAHs from contaminated sediments.

Some industrial wastewater containing complicated contents (e.g., heavy metals and organics) and extensive concentration-variation cannot be well-treated by physical-chemical treatment processes. In order to obtain the feasible electrochemical technique, an electrocatalytic-membrane process (ECMP) was established to treat such wastewater from a mint factory in Taiwan. Wastewater samples with pollutants of Cu2+, Ni2+ and chemical oxygen demand (COD) were categorized into three types based on pH and concentrations. The complexity of wastewater is attributed that a verity of chemical reagents and manufacturing methods are employed to produce different kind of coins. In this study, each type of wastewater was treated by the ECMP and integrated with other techniques to find out the appropriate procedures. Results indicate that the sole ECMP can effectively remove the Cu2+, Ni2+, and COD when the wastewater is with relatively low pH (around 3–5), low COD (around 50 mg L−1), and high concentration of heavy metals (Cu2+ concentration over 500 mg L−1). However, the ECMP should combine with pH-adjustment to effectively remove the Cu2+, Ni2+, and COD when the wastewater is with very low pH (close to 1), high COD (over 200 mg L−1), and high concentration of heavy metals. In addition, the ECMP has to link the electrocoagulation (ECG) to decrease the Cu2+, Ni2+, and COD concentration when the wastewater is with neutral pH (around 7), middle-level COD (around 130 mg L−1), and low concentration of heavy metals (Cu2+ concentration around 1.0 mg L−1). Accordingly, the ECMP integrated with other treatment processes gains potential to treat refractory wastewater.

A sustainable system capable of simultaneous removal of organic contaminants and hydrogen generation in wastewater treatment operation was studied using hematite electrode in the presence of Mn(II), PEC-Mn(II), as a proof of concept. The photoelectrochemical (PEC) system exhibited methylene blue (MB) decolorization threefold faster than that of photo-Fenton processes and yielded comparable photocurrent density to relative to the control system, i.e., PEC water splitting in the absence of MB at otherwise identical operation conditions. Furthermore, the advantages of PEC-Mn(II) system were no H2O2 addition, hydrogen production potential, and ease in Mn(II) separation via the formation of MnO2 precipitates during wastewater treatment operations. The PEC-Mn(II) process is a promising and sustainable approach toward wastewater treatment with the capability of concurrent photochemical energy generation. Moreover, the PEC-Mn(II) process can be an emerging energy-from-wastewater alternative in addition to other systems such as microbial fuel cell and anaerobic digestion.

Harbor sediments normally accumulate the pollutants from municipal and industrial activities in the estuarine zone. This work aimed to characterize the fractionation change of heavy metals in harbor sediments before and after chemical washing. Since the annual dredging around the Kaohsiung Harbor has increased over time, the influence of ex-situ acid washing on sediment quality needs to be evaluated. Experimental parameters of acid washing included the solid loading (4–20%) and types (HCl, HNO3, and citric acid) and concentrations (0.01–1 M) of acids. The fractionation of Cu, Zn, Ni, Cd, Cr, and Pb in the sediments at three estuaries, the Chienchen River, Canon River (Dock No.5), and Yanshui River, before and after washing processes were determined through sequential extraction. The washing efficiencies of HCl, HNO3, and citric acid were similar, being 80.1–83.7%, 27.6–30.9%, 20.7–23.9%, and 97.2–98.8% for Zn, Ni, Cr, and Cd, respectively. After 15 min of washing, HCl was found as a suitable washing agent, and particularly, more effective for Cu (65.3%) and Pb (79.4%) than other acids. The extraction process suggested that the acid washing of carbonate, the Fe-Mn oxide composite, and organic phases were highly correlated to their quantities in the sediments. However, the removal efficiency was inversely related to the metals in the residual phase. Knowing the mobility and bioavailability of heavy metals based on fractionation of metals benefits the assessment of the potential risk of dredged harbor sediment after the washing procedure. This study provided evidence that acid washing, as a remediation method, could be versatile in removing heavy metals from mobile phases without causing mineralogical changes to the contaminated sediments of the harbor area.

To evaluate the toxicity of sediments collected from the mouths of four rivers and entrances of Kaohsiung Harbor, Taiwan, a combination of in vitro cytotoxicity assays (Clone 9 cells) and chemical analysis that quantified 16 polycyclic aromatic hydrocarbons (PAHs), 10 phthalate esters (PAEs), and 2 alkylphenols (APs) was employed. Results showed that the total concentrations of PAHs, PAEs, and APs ranged between 77.9 and 24,363 ng/g dw, between 268 and 118,010 ng/g dw, and between 32.6 and 84,438 ng/g dw in sediments, respectively. The highest concentrations of PAHs, PAEs, and APs were found in the mouths of the Salt River (SR), Love River (LR), and Jen-Gen River (JR), respectively. Mean reference sediment quotient (m-RSQ) values were calculated using the chemical concentrations measured in the sediment of entrance I (EI) as the benchmark, and the order was SR > LR > JR > CR (Canon River mouth) > EII (entrance II) > EI. Results of the cytotoxicity assay showed that the 50% inhibitory concentration (IC50) of Clone 9 cells was in the order of LR < SR < JR < CR < EII < EI. Results on DNA content, apoptotic and autophagy protein biomarkers, and acridine orange staining indicated that the cause of death of Clone 9 cells after treatment with sediment extracts of the LR site was mainly through apoptosis. There was a significant correlation between m-RSQ values and IC50 of Clone 9 cells. The correlation analysis between cytotoxicity and chemical analytical data indicated that certain unknown chemicals may exist in LR sediment. Overall, this study demonstrated that the combination of chemical and biological analyses can provide a more comprehensive and realistic assessment of sediment toxicity to aquatic organisms compared to traditional chemistry-based-only analytical approaches.

Bi2WO6 (BW) and SnO2/Bi2WO6 composites (SnBWs) were synthesized by a single-step solvothermal process. Four SnO2/BW molar ratios, 0.1, 0.25, 0.5 and 1 were used to generate 0.1SnBW, 0.25SnBW, 0.5SnBW and 1SnBW. The surface characteristics of BW, SnO2 and SnBWs were elucidated by X-ray diffractometry (XRD), transmission electron microscopy, specific surface area analysis, UV–vis spectrophotometry, photoluminescence spectrophotometry and X-ray photoelectron spectroscopy. C.I. Reactive Red 2 (RR2) was used as a target pollutant to compare the photocatalytic activities of the prepared SnBWs. The effects of RR2 concentration and photocatalyst dosage on RR2 photodegradation were elucidated. The XRD results revealed that all of the peaks of SnBWs in XRD patterns could be assigned to SnO2 or BW, and no other peak was found, indicating that SnO2 and BW were successfully composited. The band gaps of SnO2, BW, 0.1SnBW, 0.25SnBW, 0.5SnBW and 1SnBW were estimated to be 3.75, 2.85, 2.95, 2.94, 2.93 and 2.97 eV, which correspond to RR2 photodegradation rates under simulated solar light irradiation of 0.0025, 0.0255, 0.0333, 0.0279, 0.0408 and 0.0174 min−1. 0.5SnBW had the highest photocatalytic activity in RR2 photodegradation. The RR2 photodegradation rate increased as the 0.5SnBW dose increased, but decreased as the RR2 concentration increased. The results of adding scavengers suggested that the photogenerated holes were the main oxidative species in RR2 photodegradation in the 0.5SnBW system. The findings of this study suggest that the effective suppression of the recombination of electron–hole pairs in 0.5SnBW may improve the photocatalytic activity of 0.5SnBW over those of pure BW and SnO2.

Despite the growing potential in various applications of nanobiochars, there are still concerns regarding their health effects. In this study, we used a normal human in vitro model to investigate the possible toxic effects, including pulmonary toxicity, of epithelial exposure to nanobiochars. Nano-tobacco stem-pyrolyzed biochars (nTSBs), which are generated at 500 °C, were used to analyze their potential adverse effects on the lungs. Our results demonstrated that nTSBs can cause evident cytotoxic and genotoxic effects in epithelial cells by inducing ROS formation. nTSB exposure also led to the activation of inflammatory factors. Furthermore, decreases in transepithelial electrical resistance and zonula occludens proteins after exposure to nTSBs impaired the integrity of the epithelial barrier. Increases in oxidized α1-antitrypsin in BEAS-2B cells also suggested that nTSB exposure increases the risk of chronic obstructive pulmonary disease. However, all of these adverse responses were induced by high concentrations of nTSBs. Accordingly, the pulmonary toxic potential of nTSBs occurring at high concentrations is likely not the same as that occurring at more realistic outdoor exposure concentrations. Collectively, our results indicate that the risk of nTSB toxicity is low when nTSBs are used as raw materials in commercial applications.

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.

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.

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.

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.

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.