离子交换膜处理电镀废水

本文针对电镀行业废水处理中存在的问题 ,提出了将离子交换膜应用于离子交换洗脱液的分离处理。并对各室对应物的浓度以及电流效率与时间的关系进行了探讨。结果表明 ,将该工艺应用于分离处理离子交换洗脱液 ,无论是从环境治理角度 ,还是经济效益方面分析都是一种可行的方法之一。

用于促进碱性介质中析氢反应动力学的异质结构电催化剂的合理设计

在碱性介质中,由于电极材料的较高的稳定性,电催化析氢反应(HER)具有实现大规模制氢的巨大潜力。然而,即使对于最突出的铂催化剂,HER在碱性介质中的反应动力学也比在酸性介质中慢2–3个数量级,这是由于碱性环境下质子的浓度较低。异质结构催化剂具有多种结构优势,研究表明,构建异质结构电催化剂是促进碱性HER动力学的有效策略。协同效应是异质结构的一个独特特征,这意味着一个功能活性位点作为水解离的促进剂,另一个活性位点则负责适度的氢吸附,从而协同提高HER催化性能。此外,异质结构中的每个构建模块都是可调节的,为构建最佳催化剂提供了更多的灵活性和可能性。同时,由于界面处两个组分之间存在费米能级差,可以合理地调控每个组分的电子结构,从而大幅度提高碱性介质中的HER催化性能。随着对纳米结构的深入理解,人们开发了更先进的设计策略来构建高性能异质结构电催化剂。本文综述了异质结构催化剂在碱性HER方面的最新发展,以及构建界面异质结构以促进碱性HER动力学性能的合理设计原则。我们首先介绍了HER在碱性介质中的基本反应途径,然后详细讨论了促进碱性HER动力学的新兴有效策略,包括协同效应、应变效应、电子相互作用、相工程和结构工程,最后提出了未来面向实际应用的新型异质结构催化剂设计所面临的挑战和研究机遇。

一种绿色离子交换除盐技术

该文提出了一种新型的绿色离子交换除盐技术(CFIE),以替代传统离子交换复床。结果表明该技术具有可靠的除盐性能及满意的再生效果。除盐时,可将模拟海淡水电导率从50μS/cm降低至1.2μS/cm;电再生后,失效树脂可恢复除盐能力。CFIE系统的能耗和水回收率分别处于0.70 k W·h/m3和86.9%。近中性的再生浓缩液可直接回用至上级除盐设备进水口。重复性试验表明该CFIE系统可稳定运行,长期运行后未见有性能下降。

Structure and corrosion resistance of modified micro-arc oxidation coating on AZ31B magnesium alloy

A hydrophobic surface was fabricated on a micro-arc oxidation (MAO) treated AZ31 Mg alloys via surface modification with myristic acid. The effects of modification time on the wettability of the coatings were investigated using the contact angle measuring device. The surface morphologies and structure of the coatings were evaluated using SEM, XRD and FT-IR. The corrosion resistance was investigated by potentiodynamic polarization curves and long-term immersion test. The results showed that the water contact angle (CA) increases gradually with modification time from 0 to 5 h, the highest CA reaches 138° after being modified for 5 h, and the number and size of the micro pores are decreased. The modification method hardly alters crystalline structure of the MAO coating, but improves the corrosion resistance based on the much positive potential and low current density. Moreover, the corrosion resistance and hydrophobicity can be enhanced with increasing the alkyl chain. The wetting and spreading for the alkylcarboxylate with low surface energy become easier on the micro-porous surface, and alkylcarboxylate monolayer will be formed through bidentate bonding, which changes the surface micropores to a sealing or semi-sealing structure and makes the MAO coating dense and hydrophobic. All the results demonstrate that the modification process improves the corrosion protection ability of the MAO coating on AZ31B Mg alloy.

The roles and mechanism of cocatalysts in photocatalytic water splitting to produce hydrogen

Photocatalytic hydrogen(H2)evolution via water spilling over semiconductors has been considered to be one of the most promising strategies for sustainable energy supply in the future to provide non-pollution and renewable energy.The key to efficient conversion of solar-chemical energy is the design of an efficient structure for high charge separation and transportation.Therefore,cocatalysts are necessary in boosting photocatalytic H2 evolution.To date,semiconductor photocatalysts have been modified by various cocatalysts due to the extended light harvest,enhanced charge carrier separation efficiency and improved stability.This review focuses on recent developments of cocatalysts in photocatalytic H2 evolution,the roles and mechanism of the cocatalysts are discussed in detail.The cocatalysts can be divided into the following categories:metal/alloy cocatalysts,metal phosphides cocatalysts,metal oxide/hydroxide cocatalysts,carbon-based cocatalysts,dual cocatalysts,Z-scheme cocatalysts and MOFs cocatalysts.The future research and forecast for photocatalytic hydrogen generation are also suggested.

Composite Cathode based on Mn-doped Perovskite Niobate-Titanate for Efficient Steam Electrolysis

Redox-active Mn is introduced into the B site of redox-stable perovskite niobate-titanate to improve the electrocatalytic activity of composite cathode in an oxide-ion-conducting solid oxide electrolyzer. The XRD and XPS results reveal the successful partial replacement of Ti/Nb by Mn in the B site of niobate-titanate. The ionic conductivities of the Mndoped niobate-titanate are significantly improved by approximately 1 order of magnitude in reducing atmosphere and 0.5 order of magnitude in oxidizing atmosphere compared with bare niobate-titanate at 800 ℃. The current efficiency for Mn-doped niobate-titanate cathode is accordingly enhanced by ,-25% and 30% in contrast to the bare cathode with and without reducing gas flowing over the cathode under the applied voltage of 2.0 V at 800 ℃ in an oxide-ion-conducting solid oxide electrolyzer, respectively.

Antioxidation Activities of Low-Molecular-Weight Gelatin Hydrolysate Isolated from the Sea Cucumber Stichopus japonicus

Gelatin extracted from the body wall of the sea cucumber （Stichopus japonicus） was hydrolyzed with flavourzyme. Low-molecular-weight gelatin hydrolysate （LMW-GH） of 700-- 1700 Da was produced using an ultrafiltration membrane bioreaetor system. Chemiluminescence analysis revealed that LMW-GH scavenges high free radicals in a concentration-dependent manner; IC50 value for superoxide and hydroxyl radicals was 442 and 285 μgmL-1, respectively. LMW-GH exhibited excellent inhibitory characteristics against melanin synthesis and tyrosinase activity in B16 cells. Furthermore, LMW-GH notably increased in- traeellular glutathione （GSH）, which in turn suppressed melanogenesis. LMW-GH performs antioxidation activity, holding the potential of being used as a valuable ingredient in function foods, cosmetics and pharmaceuticals or nutriceuticals.

A Simple Model to Determine the Trends of Electric Field Enhanced Water Dissociation in a Bipolar Membrane

This work is concentrated on elucidating the mechanism of the electric field enhanced water dissociation. A simple model was established for the theoretical current-voltage characteristics in water dissociation process on a bipolar membrane based on the existence of a depletion layer and Onsager's theory. Particular attention was given to the influence of applied voltage on depletion thickness and the dissociation constant. The factors on the water splitting process, such as water diffusivity, water content, ion exchange capacity, temperature, relative permittivity, etc. Were adequately analysed based on the derived model equations and several suggestions were proposed for decreasing the applied voltage in practical operation. The water dissociation tests were conducted and compared with both the theoretical calculation and the measured current-voltage curves reported in the literature, which showed a very good prediction to practical current-voltage behavior of a bipolar membrane at high current densities when the splitting of water actually commenced.

Mineralogy, liberation and leaching characteristics of iron oxide phases in an Indian diaspore sample

The removal of iron from an Indian diaspore sample was studied using magnetic separation and leaching techniques aided by an in-depth mineralogical characterization study involving quantitative mineralogical evaluation by scanning electron microscope（QEMSCAN）, electron probe micro-analyzer（EPMA） and X-ray diffraction（XRD）. The characterization studies indicate that extremely fine-sized hematite grains are associated with several other mineral phases in a complex manner with around 60% of the hematite not liberated even below the size of 38 μm limiting the scope of physical separation processes to remove the iron. Wet high intensity magnetic separation（WHIMS） studies reveal that only 49% of iron can be removed. Further, leaching studies using oxalic acid suggest that around 76% of the iron can be removed under conditions such as a solid to liquid ratio of 0.05：1, a temperature of 90 ℃ a time period of 120 min and an acid concentration of 1 mol/L. The dissolution of iron in oxalic acid is found to be controlled by chemical reaction and the activation energy is calculated as 35.15 k J/mol.

Investigation of water adsorption and dissociation on Au_1/CeO_2 single-atom catalysts using density functional theory

We examined the water adsorption and dissociation on ceria surfaces as well as ceria‐supported Au single‐atom catalysts using density functional theory calculations.Molecular and dissociative water were observed to coexist on clean CeO2and reduced Au1/CeO2?x surfaces because of the small difference in adsorption energies,whereas the presence of dissociative water was highly favorable on reduced CeO2?x and clean Au1/CeO2surfaces.Positively charged Au single atoms on the ceria surface not only provided activation sites for water adsorption but also facilitated water dissociation by weakening the intramolecular O-H bonds.In contrast,negatively charged Au single atoms were not reactive for water adsorption because of the saturation of Au5d and6s electron shells.This work provides a fundamental understanding of the interaction between water and single‐atom Au catalysts.

Purification of Organic Wastewater Containing Cu^(2+) and Cr^(3+) by a Combined Process of Micro Electrolysis and Biofilm

A complex process of micro electrolysis and biofilm was developed to continuously treat organic wastew-aters containing heavy metal ions such as Cu2+ and Or3+, and the relevant purifying mechanism was also addressed. In detail, organic materials in wastewater could be consumed as nutritious source by biofilm composed of aerobes and anaerobes. However, for heavy metal ions (Cu2+, Cr3+), part was removed by electrodeposition, and some was adsorbed on biofilm. In order to compare with the combined process of micro electrolysis and biofilm, the experimental data of micro electrolysis process (intermittent) or biofilm process (continuous) were provided, and the kinetic data of C6H12O6 (glucose) biodegradation by cultured microbes or acclimated microbes were also obtained. These experimental results indicated that for wastewater initially consisted of CeH12O6 (500mg-L-1), Cu2+ and Cr3+ (10mg-L-1), after treatment, its concentrations of C6H12O6, Cu2+ and Cr3+ were lowered to the level of 55-65mg.L^1, and less than 1mg-L-1, respectively. And the industrial reused water standards could be met by treated wastewater.

Structural and Infrared Spectroscopic Study on Solvation of Acetylene by Protonated Water Molecules

The effect of solvation on the conformation of acetylene has been studied by adding one water molecule at a time. Quantum chemical calculations of the n＋ （C2H2）（H2O）n （n=1-5） clusters indicate that the H2O molecules prefer to form the OH...Tr interaction rather than the CH...O interaction. This solvation motif is different from that of neutral （C2H2）（H2O）n （n=1-4） clusters, in which the H2O molecules prefer to form the CH...O and OH...C Hbonds. For the H＋（C2H2）（H2O）n cationic clusters, the first solvation shell consists of one ring structure with two OH...Tr H-bonds and three water molecules, which is completed at n=4. Simulated infrared spectra reveal that vibrational frequencies of OH... H-bonded O-H stretching afford a sensitive probe for exploring the solvation of acetylene by protonated water molecules. Infrared spectra of the H＋ （C2H2）（H2O）n （n=1-5） clusters could be readily measured by the infrared photodissociation technique and thus provide useful information for the understanding of solvation processes.

Latest progress in hydrogen production from solar water splitting via photocatalysis,photoelectrochemical,and photovoltaic-photoelectrochemical solutions

Hydrogen production via solar water splitting is regarded as one of the most promising ways to utilize solar energy and has attracted more and more attention. Great progress has been made on photocatalytic water splitting for hydrogen production in the past few years. This review summarizesthe very recent progress (mainly in the last 2–3 years) on three major types of solar hydrogenproduction systems: particulate photocatalysis (PC) systems, photoelectrochemical (PEC) systems,and photovoltaic‐photoelectrochemical (PV‐PEC) hybrid systems. The solar‐to‐hydrogen (STH)conversion efficiency of PC systems has recently exceeded 1.0% using a SrTiO3:La,Rh/Au/BiVO4:Mophotocatalyst, 2.5% for PEC water splitting on a tantalum nitride photoanode, and reached 22.4%for PV‐PEC water splitting using a multi‐junction GaInP/GaAs/Ge cell and Ni electrode hybrid system.The advantages and disadvantages of these systems for hydrogen production via solar watersplitting, especially for their potential demonstration and application in the future, are briefly describedand discussed. Finally, the challenges and opportunities for solar water splitting solutions are also forecasted.

Enzyme-like Activities of Algal Polysaccharide-Cerium Complexes

Water-soluble algal polysaccharides (APS) (alginic acid, fucoidan and laminaran) possess many pharmacological activities. The results of this study showed that the APS- Ce4+ complexes have some enzyme-like activities. Fucoidan and its complex with Ce4+ have activities similar to those of SOD. The activities of laminaran, alginic acid and their complexes are not measurable. The APS do not show measurable activities in the digestion of plasmid DNA. In contrast, the APS- Ce4+ complexes show these measurable activities under the comparable condition when APS bind Ce4+ and form homogenous solu-tions. The laminaran- Ce4+ complex shows the most obvious activity in the digestion of plasmid DNA, pNPP and chloropy-rifos under neutral conditions.

An Efficient and Stable Ionic Liquid System for Synthesis of Ethylene Glycol via Hydrolysis of Ethylene Carbonate

An ionic liquid system of [Bmim]X/[Bmim]OH(X Cl,BF4,and PF6,) was developed for the hydroly-sis of ethylene carbonate to ethylene glycol. The important parameters,such as the variety of ionic liquids,molar ratio of [Bmim]X to [Bmim]OH,amount of ionic liquid,molar ratio of water to ethylene carbonate,reaction tem-perature,pressure and reaction time,were investigated systematically. Excellent yield(>93%) and high selectivity(99.5%) of ethylene glycol were achieved. Under the optimum reaction conditions,the ionic liquid system could be reused at least five times and the selectivity of ethylene glycol remained higher than 99.5%.

Rational design of stratified material with spatially separated catalytic sites as an efficient overall water-splitting photocatalyst

The development of metal sulfide catalysts with remarkable activity toward efficient overall photocatalytic water splitting remains challenging owing to the dominant charge recombination and deficient catalytic active sites.Moreover,in the process of water oxidation catalysis,the inhibition of severe photocorrosion is an immense task,requiring effective photogenic hole-transfer kinetics.Herein,stratified Co-MnO_(2)@CdS/CoS hollow cubes with spatially separated catalytic sites were rationally designed and fabricated as highly efficient controllable catalysts for photocatalytic overall water splitting.The unique self-templated method,including a continuous anion/cation-exchange reaction,integrates a Co-doped oxidation co-catalyst(Co-MnO_(2))and a reduction co-catalyst(CoS)on the nanocubes with uniform interface contact and ultrathin two-dimensional(2D)nanometer sheets.We demonstrate that the stratified Co-MnO_(2)@CdS/CoS hollow cubes can provide an abundance of active sites for surface redox reactions and contribute to the separation and migration of the photoionization charge carriers.In particular,CoS nanoparticles dispersed on the walls of CdS hollow cubes were identified as reduction co-catalysts accelerating hydrogen generation,while Co-MnO_(2) nanosheets attached to the inner walls of the CdS hollow cube were oxidation co-catalysts,promoting oxygen evolution dynamics.Benefiting from the desirable structural and compositional advantages,optimized stratification of Co-MnO_(2)@CdS/CoS nanocubes provided a catalytic system devoid of precious metals,which exhibited a remarkable overall photocatalytic water-splitting rate(735.4(H_(2))and 361.1(O_(2))μmol h^(−1) g^(−1)),being among the highest values reported thus far for CdS-based catalysts.Moreover,an apparent quantum efficiency(AQE)of 1.32%was achieved for hydrogen evolution at 420 nm.This study emphasizes the importance of rational design on the structure and composition of photocatalysts for overall water splitting.

Renal elimination of organic anions in cholestasis

The disposition of most drugs is highly dependent on specialized transporters. OAT1 and OAT3 are two organic anion transporters expressed in the basolateral membrane of renal proximal tubule cells, identified as contributors to xenobiotic and endogenous organic anion secretion. It is well known that cholestasis may cause renal damage. Impairment of kidney function produces modifications in the renal elimination of drugs. Recent studies have demonstrated that the renal abundance of OAT1 and OAT3 plays an important role in the renal elimination of organic anions in the presence of extrahepatic cholestasis. Time elapsed after obstructive cholestasis has an important impact on the regulation of both types of organic anion transporters. The renal expression of OAT1 and OAT3 should be taken into account in order to improve pharmacotherapeutic efficacy and to prevent drug toxicity during the onset of this hepatic disease.

Hydrolysis of Aluminum Ions in Kaolinite and Oxisol Suspensions as Influenced by Organic Anions

To evaluate the role of kaolinite and variable charge soils on the hydrolytic reaction of Al, the hydrolysis of Al ions in suspensions of a kaolinite and an Oxisol influenced by organic anions was investigated using changes of pH, Al adsorption, and desorption of pre-adsorbed Al. Kaolinite and the Oxisol promoted the hydrolytic reaction of Al above a certain initial Al concentration (0.1 mmol L-1 for kaolinite and 0.3 mmol L-1 for the Oxisol). The Al hydrolysis accelerated by kaolinite and the Oxisol increased with an increase in initial concentration of Al and was observed in the range of pH from 3.7 to 4.7 for kaolinite and 3.9 to 4.9 for the Oxisol. The acceleration of Al hydrolysis also increased with the increase of solution pH, reached a maximum value at pH 4.5, and then decreased sharply. Al hydrolysis was promoted mainly through selective adsorption for hydroxy-Al. Soil free iron oxides compensated a portion of the soil negative charge or masked some soil surface negative sites leading to a decrease in Al adsorption, which retarded acceleration to some extent. For the Oxisol organic anions increased the proportion of adsorbed Al3+ in total adsorbed Al with the increase in soil negative surface charge and eliminated or reduced the acceleration of Al hydrolysis. Different organic anions inhibited the hydrolysis of Al in the order: citrate > oxalate > acetate (under initial pH of 4.5). The formation of Al-organic complexes in solution also inhibited the hydrolysis of Al.

Synthesis of PdS-CdSe@CdS-Au nanorods with asymmetric tips with improved H_2 production efficiency in water splitting and increased photostability

Charge separation is a crucial problem in photocatalysis.We used a wet‐chemical method to synthesize asymmetrically tipped PdS‐CdSe‐seeded CdS(CdSe@CdS)‐Au nanorod(NR)heterostructures(HCs).In these HCs,electrons and holes are rapidly separated and transported to opposite ends of the NRs by internal electric fields.Their ultraviolet‐visible absorption spectra showed strong electronic coupling between both tips and the CdS body.PdS‐CdSe@CdS‐Au achieved a H2production rate of ca.1100?mol in5h;this is two orders of magnitude greater than the rate achieved with Au‐CdSe@CdS NRs with only one tip.PdS‐CdSe@CdS‐Au NRs can withstand4h of photoirradiation,compared to1.5h for CdSe@CdS NRs,indicating that the photostability of PdS‐CdSe@CdS‐Au is much better than that of CdS.The greatly improved photocatalytic activity and stability are attributed to efficient charge separation and rapid charge transport in the PdS‐CdSe@CdS‐Au HCs.