Efficacy of acupoint injection in the treatment of chronic eczema and its influence on peripheral blood T cells.

BACKGROUND: Chronic eczema significantly impacts daily life, social interactions, and quality of life; however, no curative treatment has been identified. AIM: To determine the clinical efficacy of acupoint injection for chronic eczema and its influence on peripheral blood T cells. METHODS: Eighty patients with chronic eczema treated at our hospital between June 2022 and March 2023 were randomly assigned to a control group (n = 40), which received conventional Western medicine treatment, or an observation group (n = 40), which received routine Western medicine treatment plus acupoint injection of triamcinolone acetonide. Response and adverse reaction rates, as well as differences in the levels of serum cytokines IFN-γ, IL-2, IL-4, and IL-10 before and after treatment were investigated. RESULTS: No difference in overall response rates were found between the observation and control groups (100% vs 90%, respectively; P > 0.05); however, the observation group had a higher marked response rate than the control group (87.5% vs 52.5%; P < 0.05). Both groups had decreased Eczema Area and Severity Index scores and increased pruritus after treatment (P < 0.05), particularly in the observation group (P < 0.05). The observation group had an adverse reaction rate of 2.5% (1/40), which did not differ significantly from that of the control group (P > 0.05). The observation group exhibited higher post-treatment INF-γ and IL-2 but lower IL-4 levels than the control group (P < 0.05); however, no significant inter-group difference was observed in post-treatment IL-10 levels (P > 0.05). CONCLUSION: Acupoint injection of triamcinolone acetonide is safe and effective in treating chronic eczema. Its therapeutic mechanism is related to the regulation of peripheral blood T cell levels, inhibition of inflammatory reactions, and mitigation of immune imbalance.

Quantification and cultivation of Helicobacter pylori (H. pylori) from various urban water environments: A comprehensive analysis of precondition methods and sample characteristics.

Substantial evidence suggests that all types of water, such as drinking water, wastewater, surface water, and groundwater, can be potential sources of Helicobacter pylori (H. pylori) infection. Thus, it is critical to thoroughly investigate all possible preconditioning methods to enhance the recovery of H. pylori, improve the reproducibility of subsequent detection, and optimize the suitability for various water types and different detection purposes. In this study, we proposed and evaluated five distinct preconditioning methods for treating water samples collected from multiple urban water environments, aiming to maximize the quantitative qPCR readouts and achieve effective selective cultivation. According to the experimental results, when using the qPCR technique to examine WWTP influent, effluent, septic tank, and wetland water samples, the significance of having a preliminary cleaning step becomes more evident as it can profoundly influence qPCR detection results. In contrast, the simple, straightforward membrane filtration method could perform best when isolating and culturing H. pylori from all water samples. Upon examining the cultivation and qPCR results obtained from groundwater samples, the presence of infectious H. pylori (potentially other pathogens) in aquifers must represent a pressing environmental emergency demanding immediate attention. Furthermore, we believe groundwater can be used as a medium to reflect the H. pylori prevalence in a highly populated community due to its straightforward analytical matrix, consistent detection performance, and minimal interferences from human activities, temperature, precipitation, and other environmental fluctuations.

Long-range hydrophobic force enhanced interfacial photocatalysis for the submerged surface anti-biofouling.

Developing anti-biofouling and anti-biofilm techniques is of great importance for protecting water-contact surfaces. In this study, we developed a novel double-layer system consisting of a bottom immobilized TiO2 nanoflower arrays (TNFs) unit and an upper superhydrophobic (SHB) coating along with the assistance of nanobubbles (NBs), which can significantly elevate the interfacial oxygen level by establishing the long-range hydrophobic force between NBs and SHB and effectively maximize the photocatalytic reaction brought by the bottom TNFs. The developed NBs-SHB/TNFs system demonstrated the highest bulk chemical oxygen demand (COD) reduction efficiency at approximately 80% and achieved significant E. coli and Chlorella sp. inhibition efficiencies of 5.38 and 1.99 logs. Meanwhile, the system showed a sevenfold higher resistance to biofilm formation when testing in a wastewater matrix using a wildly collected biofilm seeding solution. These findings provide insights for implementing nanobubble-integrated techniques for submerged surface protection.

Indigenous microbial community governs the survival of Escherichia coli O157:H7 in constructed wetlands.

The survival pattern of Escherichia coli O157:H7 (E. coli O157:H7) and its regulatory factors in natural environments have been widely studied. However, there is little information about the survival of E. coli O157:H7 in artificial environments, especially in wastewater treatment facilities. In this study, a contamination experiment was performed to explore the survival pattern of E. coli O157:H7 and its central control factors in two constructed wetlands (CWs) under different hydraulic loading rates (HLRs). The results showed that the survival time of E. coli O157:H7 was longer in the CW under the higher HLR. Substrate ammonium nitrogen and available phosphorus were the main factors that influenced the survival of E. coli O157:H7 in CWs. Despite the minimal effect of microbial α-diversity, some keystone taxa, such as Aeromonas, Selenomonas, and Paramecium, governed the survival of E. coli O157:H7. In addition, the prokaryotic community had a more significant impact on the survival of E. coli O157:H7 than the eukaryotic community. The biotic properties had a more substantial direct power on the survival of E. coli O157:H7 than the abiotic factors in CWs. Collectively, this study comprehensively disclosed the survival pattern of E. coli O157:H7 in CWs, which is an essential addition to the environmental behavior of E. coli O157:H7, providing a theoretical basis for the prevention and control of biological contamination in wastewater treatment processes.

Processes of nitrogen removal from rainwater runoff in bioretention filters modified with ceramsite and activated carbon.

Conventional bioretention filters lack satisfactory performance in nitrogen removal. In this study, we used a mixture of cultivated soil and river sand as the bioretention filter to remove nitrogen pollutants from simulated rainwater runoff. To improve its permeability and nitrogen removal performance, both activated carbon and ceramsite were used as additives. The nitrogen removal processes and its mass accumulation in the modified bioretention filters were studied. The contribution of adsorption and biotransformation processes, together with the effects of percolate rate on nitrogen removal performance was explored. The results showed that an activated carbon layer in the bioretention filters could obviously improve nitrogen removal efficiencies, but its location made no significant difference in nitrogen removal performance. Bioretention filters modified with 20% of ceramsite could achieve the optimal percolate rate and nitrogen removal efficiencies. At given conditions, the average removal efficiencies of ammonium nitrogen (NH3-N), nitrate-nitrogen (NO3-N), and total nitrogen (TN) by the modified bioretention filter reached 80.27%, 41.48%, and 59.45%, respectively. During the leaching processes, organic nitrogen originated in the filter materials can be mineralised into NH3-N, then be denitrified and completely removed in the anaerobic environment under flooding conditions. Biotransformation in the modified bioretention filters caused a reduction of NH3-N removal efficiency by 15.41% and an increase of NO3-N removal efficiency by 31.03%. The modified bioretention filter can withstand a long-term operation. Compared with NO3-N and TN, the pollutant of NH3-N in rainwater runoff is not easy to form a mass accumulation in the modified bioretention filter.Highlights The modified bioretention filter showed high percolation rate and nitrogen removal.Hydraulic residence time is a critical design parameter to achieve nitrogen removal.NH3-N is not easy to form a mass accumulation in the filler media as NO3-N.Biodegradation increased NO3-N removal efficiency by 31.03% at given conditions.

Toward an intensive understanding of sewer sediment prokaryotic community assembly and function.

Prokaryotic communities play important roles in sewer sediment ecosystems, but the community composition, functional potential, and assembly mechanisms of sewer sediment prokaryotic communities are still poorly understood. Here, we studied the sediment prokaryotic communities in different urban functional areas (multifunctional, commercial, and residential areas) through 16S rRNA gene amplicon sequencing. Our results suggested that the compositions of prokaryotic communities varied significantly among functional areas. Desulfomicrobium, Desulfovibrio, and Desulfobacter involved in the sulfur cycle and some hydrolytic fermentation bacteria were enriched in multifunctional area, while Methanospirillum and Methanoregulaceae, which were related to methane metabolism were significantly discriminant taxa in the commercial area. Physicochemical properties were closely related to overall community changes (p < 0.001), especially the nutrient levels of sediments (i.e., total nitrogen and total phosphorus) and sediment pH. Network analysis revealed that the prokaryotic community network of the residential area sediment was more complex than the other functional areas, suggesting higher stability of the prokaryotic community in the residential area. Stochastic processes dominated the construction of the prokaryotic community. These results expand our understanding of the characteristics of prokaryotic communities in sewer sediment, providing a new perspective for studying sewer sediment prokaryotic community structure.

Enhanced Photocatalytic Removal of Hexavalent Chromium over Bi12TiO20/RGO Polyhedral Microstructure Photocatalysts.

A Bi12TiO20/RGO photocatalyst with polyhedron microstructure was fabricated via the template-free hydrothermal method, and the visible-light-induced photocatalytic activity of the prepared Bi12TiO20 was also evaluated by the photocatalytic reduction of heavy metal pollutants. The structures and optical properties of the prepared Bi12TiO20/RGO were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), and UV-vis diffuse reflectance spectrum (UV-vis DRS). The effects of the reaction time and mineralizer concentration on the formation of the Bi12TiO20 polyhedral microstructure were analyzed. The enhanced photocatalytic performances of Bi12TiO20/RGO were observed which were ascribed to the combination of the Bi12TiO20 microstructure induced photogenerated charges and the RGO nanostructure as a photogenerated charges carrier. The effect of organic acids, p-hydroxybenzoic acid (PHBA), chloroacetic acid, and citric acid on the Cr(VI) photocatalytic reduction was also discussed. This work provides an insight into the design of the bismuth-based microstructure photocatalyst towards the application for environment purification of heavy metals.

Kinetic and mechanistic insights into the degradation of clofibric acid in saline wastewater by Co2+/PMS process: a modeling and theoretical study.

Recently, the degradation of non-chlorinated organic pollutants in saline pharmaceutical wastewater by SO4˙--based advanced oxidation processes (AOPs) has received widespread attention. However, little is known about the oxidation of chlorinated compounds in SO4˙--based AOPs. This study chose clofibric acid (CA) as a chlorinated pollutant model; the oxidation kinetics and mechanistic pathway were explored in the Co2+/peroxymonosulfate (PMS) system. Notably, a high removal efficiency (81.0%) but low mineralization rate (9.15%) of CA within 120 min were observed at pH 3.0 during Co2+/PMS treatment. Exogenic Cl- had a dual effect (inhibitory then promoting) on CA degradation. Several undesirable chlorinated by-products were formed in the Co2+/PMS system. This demonstrated endogenic chlorine and exogenic Cl- both reacted with SO4˙- to generate chlorine radicals, which participated in the dechlorination and rechlorination of CA and its by-products. Furthermore, SO4˙- was the dominant species responsible for CA degradation at low Cl- concentrations (≤1 mM), whereas Cl2˙- was the predominant radical at [Cl-]0 > 1 mM. A possible degradation pathway of CA was proposed. Our findings suggested that chlorinated compounds in highly saline pharmaceutical wastewater will be more resistant and deserve more attention.

Impact analysis of hydraulic loading rate on constructed wetland: Insight into the response of bulk substrate and root-associated microbiota.

Constructed wetland (CW) is an environment-friendly and low-cost technology for nutrients removal from domestic wastewater. For a well-tuned CW, hydraulic loading rate (HLR) is one of the critical factors, particularly under the challenging circumstance of more frequent heavy rainfall events brought by global warming. In this study, a comprehensive investigation was conducted to explore the influence of different HLRs on the CW's bulk substrate and root-associated microbiota aiming to yield new insight for CW management from a hybrid perspective of environmental microbiology and engineering science. The response of the microbial community and associated nutrients removal performance under different HLR settings were analyzed after a one-year operation. Results showed that the bulk substrate and rhizosphere genera involved in desulfurization and denitrification, such as Ferritrophicum, Sulfurimonas, and Sulfurisoma, were enriched in the higher HLR condition and associated with the higher total nitrogen (TN) and nitrate nitrogen (NO3--N) removal compared to the lower HLR condition. Co-occurrence network analysis demonstrated a more complex network under the higher HLR condition. Besides, it was observed that more stochastic in microbial assembly under the higher HLR condition. Surprisingly, zoonotic pathogens were observed and showed a greater prevalence under the higher HLR condition, indicating the potential correlation between HLR and pathogen intrusion. Collectively, this study revealed that the microbiota could be significantly altered under different HLR conditions, thereby resulting in differences in nutrients removal performance.

Mechanically Strong and Electrochemically Stable Single-Ion Conducting Polymer Electrolytes Constructed from Hydrogen Bonding.

Herein, composite membranes based on a single-ion conducting polymer electrolyte (SIPE) and poly(vinylidene fluoride-hexafluoropropylene) (PVDF-HFP) were prepared by an electrospinning technology. The SIPE with hydrogen bonding was obtained via reversible addition-fragmentation chain transfer (RAFT) copolymerization of 2-(3-(6-methyl-4-oxo-1,4-dihydropyrimidin-2-yl)ureido)ethyl methacrylate (UPyMA), poly(ethylene glycol) methyl ether methacrylate (PEGMA), and lithium 4-styrenesulfonyl (phenylsulfonyl) imide (SSPSILi). The obtained composite membrane exhibited a highly porous network structure, superior thermal stability (>300 °C), and high mechanical strength (17.3 MPa). The fabricated SIPE/PVDF-HFP composite membrane without lithium salts possessed a high ionic conductivity of 2.78 × 10-5 S cm-1 at 30 °C, excellent compatibility with the lithium metal electrode, and high lithium-ion transference number (0.89). The symmetric Li//Li cell exhibited a superior cycle performance without short circuit, indicating the generation of a stable interface between SIPE and the lithium metal electrode during the process of lithium plating/stripping, which could inhibit lithium dendrite growth in lithium metal batteries (LMBs). The Li//LiFePO4 cell also exhibited superior cycle life and excellent rate capability at 60 or 25 °C. In consequence, the composite membrane exhibits a considerable future prospect for advanced LMBs.

A combined radical and non-radical oxidation processes for efficient degradation of Acid Orange 7 in the homogeneous Cu(II)/PMS system: important role of chloride.

Trace copper ion (Cu(II)) in water and wastewater can trigger peroxymonosulfate (PMS) activation to oxidize organic compounds, but it only works under alkaline conditions. In this work, we found that the presence of chloride could significantly accelerate the oxidation of Acid Orange 7 (AO7) by the Cu(II)/PMS process at a wide pH range (4.0-9.0). The observed pseudo-first-order rate constant k for AO7 oxidation was linearly correlated with the increased Cl- concentration (0-300 mM). An increase in mineralization rate was observed in the presence of Cl-, while the overall mineralization was quite low. Decomposition of PMS facilitated when Cl- concentration or pH value increased. Based on the scavenger experiments and electron paramagnetic resonance (EPR) measurement, the mechanism of Cu(II)-catalyzed PMS oxidation process in the presence of Cl- was proposed as both the radical and non-radical pathway, and 1O2 was the reactive oxygen species in the Cu(II)/PMS system. Finally, a possible degradation pathway of AO7 was elucidated. The feasibility of in situ utilizing high salinity and trace cupric species to accelerate the degradation of organic pollutants by the Cu(II)/PMS process in water and wastewater was demonstrated. However, the identification of undesired chlorinated by-products reminds us of cautiousness in assessing the application of Cu(II)/PMS system under chloride-rich environment. The findings of this work provide a simple and efficient approach to apply PMS in the remediation of refractory organic contaminants in the presence of trace cupric species under a high salinity environment with a wide range of pH.

Degradation and chlorination mechanism of fumaric acid based on SO4•-: an experimental and theoretical study.

It is well known that chloride ions could affect the oxidation kinetics and mechanism of contaminant based on SO4•- in the wastewater. Here, the degradation of an organic acid, fumaric acid (FA), was investigated in the presence of chloride (0-300 mM) by the Fe(II)/peroxymonosulfate (Fe(II)/PMS) system. A negative impact of chloride was observed on the rates of FA degradation. The degree of inhibitory effect was higher in Fe(II)/PMS addition order. Some chlorinated byproducts were identified during the FA oxidation process in the presence of Cl- by the ultraperformance liquid chromatography and quadrupole-time of flight mass spectrometer (UPLC-QTOF-MS). With the increasing content of Cl-, an accumulation of adsorbable organic halogen (AOX), an increase in acute toxicity, and an inhibition of mineralization were observed. According to the results of kinetic modeling, the production and transformation of oxidative species were dependent on Cl- dosage and reaction time. SO4•- was supposed to be the main radical for FA degradation with Cl- concentration below 5 mM, whereas Cl2•- was primarily responsible for the depletion of FA at [Cl-] > 5 mM. A possible degradation pathway of FA was discussed. This study reveals the potential environmental risk of organic acid and is necessary to explore useful strategies for ameliorating the treatment of chloride-rich wastewater.

Performance of permeable pavement systems on stormwater permeability and pollutant removal.

Permeable pavement is an effective means for stormwater runoff control and pollutant removal. However, relatively few studies have examined the characteristics of permeable brick and corresponding permeable pavement system (PPS). In this work, the permeable pavement systems consisted of surface permeable brick layer (concrete or ceramic) with structural layer (including a cement mortar layer, a permeable concrete layer, and a gravel layers) were selected as typical cases to assess their permeability and runoff pollutant removal performance by laboratory experiments. The results indicated that PPS had obvious outflow hysteresis effect. The PPS with ceramic brick layer reached the saturation flow rate earlier and showed larger outflow rate than that with concrete brick layer. Both types of PPSs had a relatively high efficiency (83.8-95.2%) in removing suspended solids (SS) in stormwater runoff mainly due to the interception and filtration of the surface brick layer, whereas the structural layer of the PPS played a vital role in the removal of total phosphorus (TP). The percentage of total nitrogen (TN) removal efficiency via ceramic brick layer accounted for via corresponding PPS was obviously larger than that of concrete brick layer. The PPS also displayed a certain chemical oxygen demand (COD) removal ability: around 14.0-27.0% for concrete type and 20.9-28.9% for ceramic type. Subsequently, a multi-objective evaluation model was implemented based on the analytic hierarchy process (AHP) method to identify the optimal scheme in relation to four indices: permeability, environmental benefit, compressive strength, and comprehensive economic cost. The results showed, insofar, the ceramic PPS is preferred with a better economic performance. Our study attempts to select optimal designs of PPS and provides insight into the permeable capacity and the efficiency of pollutant removal in PPS.

Stabilizing Liquid Electrolytes in a Porous PVDF Matrix Incorporated with Star Polymers with Linear PEG Arms and CycloPEG Cores.

Porous membranes fabricated from poly(vinylidene fluoride) (PVDF) and a star polymer with linear poly(ethylene glycol) (PEG) arms and cycloPEG cores were fabricated via the phase-separation method. The porous gel polymer electrolytes (PGPEs) were obtained by immersing the porous membranes in the electrolyte solution. When the additive amount of star polymer was up to 20 wt %, the prepared membrane had the largest porosity and the pores were uniformly distributed in the membrane. The star polymer can not only decrease the crystallization of PVDF and enhance the absorption of liquid electrolyte but also offer ion conduction channels (cycloPEG cores). Therefore, the PGPE with 20 wt % star polymers exhibited competitive ionic conductivities of 1.27 mS cm-1 at 30 °C and 2.89 mS cm-1 at 80 °C. To stabilize the liquid electrolyte in the holes of porous membranes, a gelator was introduced in the liquid electrolyte to form gelled porous gel polymer electrolytes (GPGPEs), and the leakage of liquid electrolytes was thus remarkably reduced. The ionic conductivity of GPGPEs with 20 wt % star polymer and 1.5 wt % gelator was importantly improved at high temperatures (6.02 mS cm-1 at 80 °C). We systematically investigated the electrochemical performances of PGPEs without star polymer, PGPEs with star polymer, and GPGPEs with star polymer. The incorporation of star polymers with linear PEG arms and cycloPEG cores into the PGPEs and GPGPEs significantly improved the electrochemical performances of the lithium metal/LiFePO4 cell assembled with the PGPEs or GPGPEs.

Removal of acenaphthene from wastewater by Pseudomonas sp. in anaerobic conditions: the effects of extra and intracellular substances.

Sorption and degradation are considered two primary modes of pollutant removal by microorganisms, and extracellular polymeric substances (EPS) have been shown to play an important role in these biological processes. However, their role in removing refractory organic pollutants the effects of intracellular substances in microorganisms remain unclear. In this study, we investigated both the removal mechanism and intracellular substances involved in removing the pollutant acenaphthene (ACE) from Pseudomonas sp. bacteria in anaerobic conditions. The results indicated that the ACE was mainly adsorbed rather than degraded by bacteria. Moreover, ACE had little impact on EPS secretion at concentrations ranging 0-3 mg/L. Cell walls and membranes accounted for more than 70% of ACE adsorption, whereas intra-cellular substances accounted for about 10-25% and the effect of other components on ACE adsorption was not obvious. A possible mechanism of ACE removal by bacteria is proposed.

Effect of Organic Substrates on the Photocatalytic Reduction of Cr(VI) by Porous Hollow Ga2O3 Nanoparticles.

Porous hollow Ga2O3 nanoparticles were successfully synthesized by a hydrolysis method followed by calcination. The prepared samples were characterized by field emission scanning electron microscope, transmission electron microscope, thermogravimetry and differential scanning calorimetry, UV-vis diffuse reflectance spectra and Raman spectrum. The porous structure of Ga2O3 nanoparticles can enhance the light harvesting efficiency, and provide lots of channels for the diffusion of Cr(VI) and Cr(III). Photocatalytic reduction of Cr(VI), with different initial pH and degradation of several organic substrates by porous hollow Ga2O3 nanoparticles in single system and binary system, were investigated in detail. The reduction rate of Cr(VI) in the binary pollutant system is markedly faster than that in the single Cr(VI) system, because Cr(VI) mainly acts as photogenerated electron acceptor. In addition, the type and concentration of organic substrates have an important role in the photocatalytic reduction of Cr(VI).

Treatment of facial telangiectasia with narrow-band intense pulsed light in Chinese patients.

Objective: To evaluate the efficacy and safety of narrow-band intense pulsed light (DPL) in treating facial telangiectasia. Method: Thirty patients with facial telangiectasia underwent five sessions of treatment with DPL (500 nm～600 nm) at 4-week interval. The erythema index (EI), temperature, transepidermal water loss (TEWL), and lightness of the skin (L) were measured before each treatment session and at each follow-up. Result: Thirty cases completed treatment and follow-ups. Twenty-seven cases (90%) got more than 50% clearance post-treatment and among them eight cases (27%) got more than 75% clearance. The average of the mean EI value decreased with the number of treatment sessions; the EI observed after two treatment sessions was significantly different from that observed before treatment (P = 0.012, P < 0.05). The decrease in skin temperature and TEWL values post-treatment was statistically significant (P = 0.000, P = 0.027, P < 0.05), while the L value increased significantly (P = 0.025, P < 0.05). Thirty percent cases had reccurence at 6-month follow-up. While burning sensation, erythema, and swelling were usually seen during the treatment, no severe side effects were observed during treatment and follow-ups. Conclusion: Narrow-band intense pulsed light DPL is effective and safe in treating facial telangiectasia.

An improved biofilter to control the dissolved organic nitrogen concentration during drinking water treatment.

Dissolved organic nitrogen (DON) is a key precursor of numerous disinfection by-products (DBPs), especially nitrogenous DBPs (N-DBPs) formed during disinfection in drinking water treatment. To effectively control DBPs, reduction of the DON concentration before the disinfection process is critical. Traditional biofilters can increase the DON concentration in the effluent, so an improved biofilter is needed. In this study, an improved biofilter was set up with two-layer columns using activated carbon and quartz sand under different influent patterns. Compared with the single-layer filter, the two-layer biofilter controlled the DON concentration more efficiently. The two-point influent biofilter controlled the DON concentration more effectively than the single-point influent biofilter. The improved biofilter resulted in an environment (including matrix, DO, and pH) suitable for microbial growth. Along the depth of the biofilter column, the environment affected the microbial biomass and microbial activity and thus affected the DON concentration.

Enhanced visible-light-driven photocatalytic inactivation of Escherichia coli by Bi2O2CO3/Bi3NbO7 composites.

The Bi2O2CO3/Bi3NbO7 (BiCO/BiNbO) composite was successfully fabricated by a simple hydrothermal method and found to be an effective visible-light-driven photocatalyst for inactivation of Escherichia coli (E. coli). The BiCO/BiNbO composite was characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), high-resolution transmission electron microscopy (HRTEM), UV-vis diffuse reflectance spectrum (UV-vis DRS), and Fourier transform infrared (FT-IR) spectroscopy. The BiCO/BiNbO composite exhibited largely enhanced photocatalytic inactivation of E. coli as compared to the pure Bi3NbO7 under visible light irradiation. The enhanced photocatalytic performance can be attributed to the improved separation efficiency of the photogenerated holes and electrons. In addition, the possible bactericidal mechanism of the BiCO/BiNbO composite under visible light irradiation was discussed.

Micro/nano-structured CaWO4/Bi2WO6 composite: synthesis, characterization and photocatalytic properties for degradation of organic contaminants.

The micro/nano-structured CaWO(4)/Bi(2)WO(6) composite was successfully synthesized by a one-step hydrothermal route without using any templates or surfactants. The as-prepared samples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), UV-vis diffuse reflectance spectroscopy (UV-vis DRS), Fourier transform infrared (FT-IR) spectroscopy, thermogravimetry-differential scanning calorimetry (TG-DSC) and Brunauer-Emmet-Teller (BET) theory. The results indicated that the composite has a two-phase composition: CaWO(4) and Bi(2)WO(6). The photocatalytic activities of the CaWO(4)/Bi(2)WO(6) composite were evaluated for the degradation of Rhodamine B (RhB) dye and 4-nitrophenol (4-NP) in aqueous solution under visible-light irradiation (>420 nm), which were 4.5 times and 2.5 times higher than that of the pure Bi(2)WO(6), respectively. On the basis of the calculated energy band positions, the mechanism of enhanced photocatalytic activity for the micro/nano-structured CaWO(4)/Bi(2)WO(6) composite can be attributed to the effective separation of electron-hole pairs.