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Due to the increased human activities in burning of fossil fuels and deforestation, the CO2 level in the atmosphere gets increased up to 415 ppm; although it is an essential component for plant growth, an increased level of CO2 in the atmosphere leads to global warming and catastrophic climate change. Various conventional methods are used to capture and utilize CO2, among that a feasible and eco-friendly technique for creating value-added products is the CO2RR. Photochemical, electrochemical, thermochemical, and biochemical approaches can be used to decrease the level of CO2 in the atmosphere. The introduction of nano-catalysts in the reduction process helps in the efficient conversion of CO2 with improved selectivity, increased efficiency, and also enhanced stability of the catalyst materials. Thus, in this mini-review of nano-catalysts, some of the products formed during the reduction process, like CH3OH, C2H5OH, CO, HCOOH, and CH4, are explained. Among different types of metal catalysts, carbonaceous, single-atom catalysts, and MOF based catalysts play a significant role in the CO2 RR process. The effects of the catalyst material on the surface area, composition, and structural alterations are covered in depth. To aid in the design and development of high-performance nano-catalysts for value-added products, the current state, difficulties, and future prospects are provided.

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Bismuth, a heavy metal which is found to be inexpensive and at a reduced cost, is utilized in the synthesis of different nanomaterials with novel structure, remarkable physical and chemical properties, adjustable bandgap, notable efficiency for photothermal conversion. These characteristics have made this element desirable for various applications such as storage and conversion of energy, electronics, sensors, photocatalysis, and other biomedical applications. These review papers are the vital points for the students, this report guides them to the research papers which focus on the impressive development in the area of bismuth and similar nanostructures. The purpose of the present review is to discuss the various synthesis routes of bismuth-based nanomaterials along with green synthesis, different nanostructures of bismuth, their significant properties, diverse applications and directions for the upcoming research. Therefore, with these different tuneable synthesis methods of bismuth-based nanomaterials combined with their novel properties, would elucidate on the future devices based on various nanostructures of bismuth.

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In the current work, we present the facile one-pot synthesis of 0.0, 0.5, 1.0, 2.0 and 3.0 wt% of Ni doped ZnO nanoparticles (Ni:ZnO NPs) through combustion route at 550 °C. Structural and vibrational studies approve the synthesis of monophasic hexagonal Ni:ZnO NPs. The crystallite size was calculated to be in the range of 36-60 nm for pure and doped samples. The composition of all elements in the final product along with their homogeneity, was approved through EDX/FESEM e-mapping analysis. The morphology and phase confirmation of the prepared samples was investigated through FESEM and TEM/HRTEM analyses. TEM/HRTEM study shows that the size of grains is within the range of 100 nm and grown along the c-axis as the lattice spacing is found ∼2.6005 Å. Diffused reflectance study was used to estimate the energy gap for all samples and found to reduce from 3.287 eV for pure to 3.258 eV for 3.0 wt% Ni doping. From an applications point of view, the photocatalytic performance of Ni:ZnO NPs was studied, and with 3.0 wt% of Ni doping in ZnO the degradation of methylene blue (MB) and tetracycline (TCN) pollutants were found to be remarkably improved.

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The present report investigates the various MoO3 morphologies prepared via different approaches such as morphologies are cubic sheet, ribbon, and hexagonal sheet. These prepared nanostructures are modified as a MoO3/Ni-F electrode used to detect hydrogen peroxide (H2O2). The influence of the morphology on the microstructural, morphological, electronic state, optical and electrochemical properties of MoO3 nanostructures are systematically studied. The recorded XRD spectra confirmed that the good crystalline nature with the orthorhombic crystal structure. The FESEM analysis shows that preparation approaches strongly influenced the MoO3 morphology. The elemental mapping and XPS analysis confirm the formation of MoO3. The obtained optical band gap values show that the MoO3 morphology-based bandgap values are 3.38, 3.17, and 2.94 eV. The modified MoO3/Ni-F electrode electrochemical impedance spectra show the CP-MoO3 has good conductivity. Moreover, the CP-MoO3/Ni-F electrode has a wide detection window, long-term stability, reproducibility, and a low detection limit is 1.2 µM. Hence, the CP-MoO3/Ni-F electrode electrochemical results suggest that the modified electrode has offered a good matrix for toxic contaminants sensing applications.

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This study evaluated the use of magnetite (Fe3O4), carbon black (CB), and Fe3O4-CB composites activated by persulfate (PS) at circumneutral pH to oxidize polycyclic aromatic hydrocarbons (PAHs) in marine sediments. In addition, the in vitro cytotoxic activity and apoptotic response of the obtained degradation products were investigated. Chemical analyses showed that the total PAH concentration was 26,263 ng/g for sediment samples from an industrial port area. Highly toxic BaP was the main contributor to the TEQ in sediments. Source analyses demonstrated that the PAHs in the sediment were derived from coal combustion. In this study, we found that the PS oxidation processes effectively degrade PAHs at concentration levels of 1.7 × 10-5 M at pH 6.0. The 3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyltetrazolium bromide (MTT) assay was employed to assess the cytotoxicity of the PAH degradation products before and after Fe3O4/PS, CB/PS, and Fe3O4-CB/PS oxidation treatment using a human hepatoma carcinoma cell line (HepG2) and a zebrafish (Danio rerio) embryonic cell line (ZF4). Each sample extract showed a marked dose-related response, with the cell viability reduced by 82% in the case of HepG2 and 58% in the case of ZF4 at 100 µg/mL after the Fe3O4-CB/PS process. The PAH degradation products had different effects on the cell morphologies of the two cell lines. The results suggested that the ZF4 cell model is more sensitive than HepG2 to the toxicity of the PAH samples.

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This study applied a circulation-enhanced electrokinetics (CEEK) technique to remove heavy metal lead from the agricultural land. Soil samples (lead concentration around 4000 mg/kg) were collected in a certain polluted agricultural site in Nantou, Taiwan. Operational parameters of CEEK such as the voltage gradient (1.0 V/cm), the concentration of working solution (EDTA), and pH buffer (0.01 M Na2CO3) were controlled. The CEEK with EDTA can maintain at relatively neutral pH to beneficially remove heavy metals due to appropriate EO flow, electromigration, and EDTA complexation. EDTA served as the chelating agent to react with lead in soils and its concentration plays the key factor for desorbing heavy metals from soils; the 0.1 M EDTA can achieve 79% of Pb depletion (from 3703 mg/kg to 781 mg/kg). The stoichiometric calculation can be roughly used to estimate the Pb removal efficiency based on the 1:1 M ratio of Pb to EDTA and ignores other reactions between EDTA and soil constituents. The CEEK technique with 0.1 M EDTA can remove 63% Pb (from 3430 mg/kg to 1260 mg/kg) within 6-day treatment.

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The main objective of this study was to evaluate the effect of different pyrolysis temperatures on the formation of polycyclicaromatichydrocarbons (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.

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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.

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Some agricultural lands have been contaminated by heavy metals in Taiwan for several decades, because the irrigation system was polluted by wastewater. In this study, a circulation-enhanced electrokinetics (CEEK) and phytoremediation were applied alternately to the real lead-contaminated site. In the beginning, the CEEK was used; then, the corn plants were raised. After this phytoremediation, the CEEK was employed again. Experimental results show that the lead concentration can be reduced from 5672 mg/kg to 2083 mg/kg (around 63%) after the three-stage treatment (CEEK + corn + CEEK). At each stage, CEEK, corn plants, and CEEK can remove around 25%, 5%, and 30% lead from the soil, respectively. During the whole process, the soil pH can maintain around neutral range and the electrical conductivity of soil was stable. The electricity consumption of the CEEK was quite low (89 USD per ton) and the corn plants still were alive throughout the remediation.

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This study investigated the spatial distribution of di-(2-ethylhexyl) phthalate (DEHP), and its potential biological effects, in the surface sediments that were collected from 10 sites at the Love River during dry and wet seasons. The grain size and organic matter were measured to understand the key factors that affect the distribution of DEHP concentrations in the sediments of Love River. The mean DEHP concentrations in the sediments that were collected during the wet and dry seasons were 28.6 ± 19.5 and 17.8 ± 11.6 mg/kg dry weight, respectively. The highest DEHP concentration was observed in the sediments that were sampled in the vicinity of the estuary. The correlation analysis showed that the grain size and organic matter may play a key role in the DEHP distribution in the sediments during the dry season, whereas the DEHP concentrations in the wet season may be mainly affected by other environmental and hydrological conditions. By a comparison with the sediment quality guidelines, the levels of DEHP in the sediments of Love River were found to have the potential to result in an adverse effect on aquatic benthic organisms. Specifically, during the wet season, wastewater from upstream of Love River is flushed downstream, causing a higher DEHP concentration in the sediments. Future pollution prevention and management objectives should move towards reducing the discharge of upstream wastewater and establishing a complete sewer system to reduce DEHP pollution in the environment.

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This study applied circulation-enhanced electrokinetics (CEEK) technique to remove Cd and Pb from the real-site contaminated soils. Soil samples were collected in certain polluted agricultural land in Yunlin, Taiwan. The CEEK system mainly composed of a reactor fulfilling soil samples, one pair of electrodes, a circulation system of working solution and DC power supply. Results demonstrate that the real-site Cd and Pb contaminated soils can be effectively treated by the CEEK technique; the removal efficiency of Cd and Pb can reach 91% and 85%, respectively. The CEEK system can maintain relatively neutral pH of treated soils. The bonding patterns of heavy metals and H+ produced on the anode play the critical roles for removal efficiency. The recovery efficiency of Cd and Pb in the CEEK system can reach 85% and 70%; the species of recovered heavy metals is Cd(OH)2 and Pb5O8, respectively.

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The occurrence of antibiotics in the environment has recently raised serious concerns regarding their potential threat to human health and aquatic ecosystem. A new magnetic nanocomposite, Fe3O4@C (Fe3O4 coated with carbon), was synthesized, characterized, and then applied to remove five commonly-used sulfonamides (SAs) from water. Due to its combinational merits of the outer functionalized carbon shell and the inner magnetite core, Fe3O4@C exhibited a high adsorption affinity for selected SAs and a fast magnetic separability. The adsorption kinetics of SAs on Fe3O4@C could be expressed by the pseudo second-order model. The adsorption isotherms were fitted well with the Dual-mode model, revealing that the adsorption process consisted of an initial partitioning stage and a subsequent hole-filling stage. Solution pH exerted a strong impact on the adsorption process with the maximum removal efficiencies (74% to 96%) obtained at pH 4.8 for all selected SAs. Electrostatic force and hydrogen bonding were two major driving forces for adsorption, and electron-donor-acceptor interactions may also make a certain contribution. Because the synthesized Fe3O4@C showed comprehensive advantages of high adsorptivity, fast magnetic separability, and prominent reusability, it has potential applications in water treatment.

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A 20-40 nm anatase-titania film on a titanium electrode was fabricated using chemical vapor deposition (CVD). The film was characterized using field emission scanning electron microscopy (FESEM), X-ray diffraction (XRD), and atomic force microscopy (AFM). The CVD deposition time and number of deposition coatings were evaluated to establish the appropriate film fabrication parameters. Results indicate that two coatings at a deposition time of 6h each produced the best nano-TiO(2) electrode films (NTEFs) with an even distribution of ca. 20 nm diameter nanoparticles in the anatase lattice. The NTEF was tested as an electrocatalytic anode to investigate the degradation efficiency in treating methyl orange dye wastewater. A high removal efficiency of methyl orange dye and total organic carbon (TOC) of 97 and 56%, respectively; was achieved using a current density of 20 mA cm(-2) for 160 min. Cyclic voltammetry showed that the electrochemical degradation reaction rate at the NTEF surface was predominately driven by molecular diffusion. The electrocatalytic decomposition rate of organic pollutants at the NTEF is controlled by mass transport, which was associated with the nanostructure of the electrocatalytic electrode.

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This research is intended to decompose organic substances in municipal wastewater with nano- and nonnano-scale electrocatalytic electrodes. As an anode, the nano-scale electrodes included lab-made TiO(2) and Cu(2)O electrodes; the nonnano-scale electrodes were a commercial TiO(2) and graphite plate. According to experimental results, the nano- and nonnano-scale catalytic electrodes can effectively remove the organic pollutants in the municipal wastewater. The perforated TiO(2) electrode is the best for eliminating the chemical oxygen demand (COD), and its efficiency is about 90% (COD decreases from 400 to 40 mg L(-1)). The conductivity of municipal wastewater and the electro-catalytic process will increase the pH and eventually remains in the neutral range. The conductivity of municipal wastewater can be lowered to some degrees. The most attractive discovery of electro-catalytic process is that the dissolved oxygen (DO) in the municipal wastewater can be increased by the TiO(2) electrode (nonnano-scale) around 4-6 mg L(-1), but few DO is produced by the nano-scale electrocatalytic electrode.

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For electrokinetics remediation, the acid produced at the anode due to the water electrolysis will cause the soil acidification and destroy the soil constituents. Especially, the contaminated soils in Taiwan are usually agricultural lands; it is necessary to improve the performance of EK system to maintain the soils nature after remediation. In this study, a circulation-enhanced EK system (CEEK) was designed to neutralize the pH of the working solution and soils. Experiments were conducted by the control of different electrolyte species (sodium and potassium salts) and concentrations (10(-3) to 5x10(-2)M), respectively. Experimental results show the operational characteristics include: the CEEK system can effectively stabilize the pH of processing solution at neutral range and the current can be maintained at stable status with carbonate salts; the pH buffering range of working solution in the CEEK system depends on the electrolyte species and their concentration significantly; the water content remains roughly as their original nature in the CEEK system. For consideration of electrochemical reactions, the water electrolysis is the predominating electrochemical reaction in the CEEK system, which not only influences the pH but also the conductivity of the working solution. In the application of practical engineering, there exist linear relationships between the pH, conductivity, current and the electrolyte concentration, respectively, which can serve as a means to assist engineers to select operational parameters of CEEK.

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Electrokinetics (EK) is a technique for soil remediation. However, the acid produced due to the water electrolysis at the anode will cause soil acidification, which may destroy the soil constituents, and reduce contaminant removal efficiency. The formation of a base front produced at the cathode will result in the precipitation of metal hydroxides and a concomitant clogging of pore space. In this study, a circulation-enhanced EK (CEEK) system is designed to neutralize the pH of the working solution and soils for avoiding the above problems. Experiments are conducted by controlling different voltage gradients, electrode materials, and electrode emplacement, respectively. According to the experimental results, the CEEK system could effectively stabilize the current and the pH of processing solution at a neutral range. The strength of voltage gradient is proportional to the current magnitude of the CEEK system. The graphite electrode for CEEK is the better choice than the metal electrodes because graphite electrodes can achieve the lower electricity consumption. The electrode installed in the reservoir without attachment on soils can decrease the pH deviation of the soil matrix.

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This research was conducted to evaluate an integrated technique, combination of the electrokinetics (EK) and zero-valent metal (ZVM), for remediation of the perchloroethylene (PCE) contaminated soils. Various experimental conditions were controlled such as different voltage gradients, the position of ZVM, and ZVM species. The appropriate operational parameters are concluded as follows: (1) 0.01 M sodium carbonate serves as the working solution; (2) the voltage gradient is controlled at 1.0 V/cm; (3) ZVM wall is settled close to the anode. Based on the above operation conditions, the pH value of working solution can maintain at neutral range for avoiding the soil acidification. Neutral pH also causes the system to stay at a stable status of electricity consumption. The removal efficiency reaches 99% and 90% for decontaminating the PCE in the pore-water and the soil, respectively, after a 10-day treatment. The zero-valent zinc performs better PCE degradation than zero-valent iron. Moreover, the soils treated by EK+ZVM still possess their original properties.

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This study is to establish optimal conditions for the minimization of iron sludge produced in Fenton oxidation processes by electro-regenerating Fe(2+) with constant potential (CPM) or constant current mode (CCM). Results indicate that the optimal cathodic potential for Fe(2+) regeneration is -0.1 V vs. the saturated calomel electrode (SCE) in terms of current efficiency. Keeping the initial Fe(3+) concentration ([Fe(3+)](0)) constant, the average current density produced at -0.1 V vs. SCE (CPM) is approximately equal to the optimal current density applied in the CCM. The suitable pH range is below the pH value determined by Fe(3+) hydrolysis. As expected, increasing cathode surface area and solution temperature notably increases Fe(2+) regeneration rate. At the optimal potential, the average current density increases linearly with [Fe(3+)](0), exhibiting a slope of 8.48 x 10(-3)(A/m(2))(mg/L)(-1). The average current efficiency varies with [Fe(3+)](0), e.g., 75% and 96-98% at 100 and > or = 500 mg/L [Fe(3+)](0), respectively. Once reaching 75% of Fe(2+) regeneration capacity, further regeneration becomes difficult due to Fe(3+) mass transfer limitation. Fe(2+) can also be effectively regenerated by dissolving iron sludge at low pH (usually

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Hydrogen peroxide (H2O2) was electro-generated in a parallel-plate electrolyzer by reduction of dissolved oxygen (DO) in acidic solutions containing dilute supporting electrolyte. Operational parameters such as cathodic potential, oxygen purity and mass flow rate, cathode surface area. pH, temperature, and inert supporting electrolyte concentration were systematically investigated as to improve the Faradic current efficiency of H2O2 generation. Results indicate that significant self-decomposition of H2O2 only occurs at high pH (> 9) and elevated temperatures (> 23 degrees C). Results also indicate that the optimal conditions for H2O2 generation are cathodic potential of -0.5 V vs. saturated calomel electrode (SCE), oxygen mass flow rate of 8.2 x 10(-2) mol/min, and pH 2. Under the optimal conditions, the average current density and average current efficiency are 6.4A/m2 and 81%, respectively. However, when air is applied at the optimal flow rate of oxygen, the average current density markedly decreases to 2.1 A/m2, while the average current efficiency slightly increases to 90%. The limiting current density is 6.4 A/m2, which is independent of cathode geometry and surface area. H2O2 generation is favored at low temperatures. In the concentration range studied (0.01-0.25 M), the inert supporting electrolyte (NaClO4) affects the total potential drop of the electrolyzer, but does not affect the net generation rate of H2O2.

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