二氧化碳的等离子体化学固定化(英文)

二氧化碳排放控制和化学利用是全世界科学家面临的难题。人们已提出利用物理和生物方法来解决二氧化碳问题，但对二氧化碳这样一个巨大的碳资源，还没有特别有效的化学利用方法。在这方面，前人曾考虑过非均相催化。但非均相催化能耗大，而氢源紧缺；以及二氧化碳本身非常稳定，需高温激活，而高温又导致催化剂寿命很有限，很难达到工业化要求。而冷等离子体，包括各种气体放电现象，其某些作用方式类似于常规催化，但在低温高效激活二氧化碳方面更有效率。本文详细讨论了等离子体二氧化碳化学固定化的各种方法，包括直接法和间接法，并比较了等离子体法与常规催化方法的区别。讨论的物系包括：Ｈ２／ＣＯ２、ＣＨ４／ＣＯ２。

HRP的电化学固定化及HRP/P-OPD酶电极的性能

利用电化学固定化方法制备含辣根过氧化物酶的聚邻苯二胺（ＨＲＰ／Ｐ－ＯＰＤ）膜电极，改变聚合用溶液的酸度和所含支持电解质的成分，研究酶的固定化过程及其对所得酶电极性能的影响．结果表明依电聚合条件而异，酶可能以不同途径进入聚合物基质中．支持电解质的品种会影响酶膜的形成速度、组成和稳定性．所得ＨＲＰ／Ｐ－ＯＰＤ膜电极可在溶液不含电子传递体的条件下催化Ｈ２Ｏ２的还原。

固定化活性氧化镧的化学除磷及其真空再生技术研究

为降低污水除磷成本、再生循环利用高效除磷剂、回收水体中磷,在此提出并研究了一种新型的化学除磷技术——固定化活性氧化镧(La2O3)化学除磷及其真空再生技术。该技术利用电解实现镧的固定,运用真空原理,实现氧化镧的再生和磷的回收。通过归纳各种常规除磷和新型除磷方法的特点,以及新型除磷方法的技术可行性,得出固定化活性La2O3化学除磷法较常规的除磷方法运行成本低,无污泥及二次污染产生,除磷效率高,可循环利用氧化镧除磷剂,回收利用水中的磷。

电聚吡咯固定化酪氨酸酶电极的制备及性能

在应用恒电位法电化学聚合吡咯的同时 ,将酪氨酸酶固定在导电聚吡咯膜内 ,制成一种灵敏、稳定的酪氨酸电极 .讨论了溶液 pH值和聚合电位对酶固定化的影响 ,对酶分子嵌入吡咯膜前后的SEM图和CV曲线进行了分析、比较 .该电极对甲苯酚响应的线性范围为 5 .0× 10 -8～ 1.0× 10 -6mol/L ,最适 pH值为 6 .6 ,酶反应表观上遵循Michaelis_Menten动力学 ,表观米氏常数为 2 .2× 10 -5mol/L .

电聚吡咯固定化酪氨酸酶电极的制备及性能

用恒电位法在电化学聚合吡咯的同时，将酪氨酸酶固定在导电聚吡咯膜内，制成一种灵敏、稳定的酪氨酸酶电极。讨论了溶液ｐ Ｈ 值和聚合电位对酶固定化的影响，对酶分子嵌入前后吡咯膜的 Ｓ Ｅ Ｍ 图和 Ｃ Ｖ 曲线进行了分析和比较。该电极响应对甲苯酚的线性范围为５ ．０ ×１０ － ８ ～１ ．０ ×１０ － ６ ｍｏｌ· Ｌ－ １ ，最适ｐ Ｈ 值为６ ．６ ，酶反应表观上遵循 Ｍｉｃｈａｅｌｉｓ＿ Ｍｅｎｔｅｎ 动力学，表观米氏常数为２ ．２ ×１０ － ５ ｍｏｌ· Ｌ－ １ 。

化学还原固定化土壤地下水中六价铬的研究进展

化学还原法在受铬污染土壤地下水系统修复过程中应用广泛。化学还原固定化方法通过将溶解度大、迁移性强的六价铬(Cr(VI))还原转化为稳定的三价铬(Cr(III))氢氧化物,从而实现铬污染控制与修复的目的。常用的还原剂包括:含铁类还原剂(零价铁、纳米零价铁和亚铁类还原剂)、还原性硫化物(H2S、Fe Sx、硫代硫酸盐和多硫化合物等)及一些具有还原活性的有机物。本文系统地综述了不同还原剂对六价铬还原固定化的机理、影响因素、修复效果及适用范围;重点对常用还原剂的优缺点进行了比较,并提出了存在的问题和今后的发展方向。

血红蛋白/聚邻苯二胺膜电极的制备及其电催化性能的研究

用固定化方法在 0 .0 5mol/L硫酸介质中制备了血红蛋白 /聚邻苯二胺膜 (Hb/PPD)电极 .所得电极呈现良好的生物催化活性 ,具有典型的酶催化反应动力学特征 .固定化Hb的转移速率常数是Hb的 5 1.9% ,在 4℃下保存 5 0d ,还保持 91.2 %的活性 .研究了不同制备条件对酶电极性能的影响 ,分析了电极上Hb催化反应的动力学 ,探讨了电极电位下Hb的催化活性 。

辣根过氧化物酶／聚邻苯二胺膜电极的制备与性能研究

辣根过氧化物酶（ＨＲＰ）／聚邻苯二胺（ＰＰＤ）膜电极由ｐＨ７．０磷酸盐缓冲溶液介质中邻苯二胺在玻碳电极上的电聚合而制得。讨论了ＨＲＰ电化学固定化的过程。所得酶电极呈现生物催化活性，可在没有电子传递体存在的情况下催化Ｈ＿Ｏ＿２还原。该反应发生在聚邻苯二胺氧化还原的电位区，聚合物参与了酶的电子转移过程。分析了旋转ＨＲＰ／ＰＰＤ电极上酶反应的动力学，讨论了动力学常数的影响因素。

动态监测清醒自由活动大鼠纹状体细胞外液乙酰胆碱和胆碱水平的方法

目的 建立动态监测正常清醒自由活动大鼠纹状体细胞外液中乙酰胆碱 (ACh)和胆碱 (Ch)水平的方法。方法 应用脑内微透析与高效液相色谱 (HPLC ) 柱后固定化酶反应器 (IMER ) 电化学检测法 (ED)相结合的技术 ,动态监测正常清醒自由活动大鼠纹状体细胞外液中ACh和Ch水平。结果 大鼠纹状体细胞外液中ACh和Ch浓度在灌流开始时较高 ,然后逐渐降低 ,ACh在灌流进行 2 4 0min后达到较稳定水平 ;Ch浓度则在灌流的 4 5 0min内持续下降。HPLC IMER ED检测ACh和Ch的极限可达 15 0fmol,且至少在 0 12 5～ 1 0 μmol·L-1的范围内线性关系良好。结论 HPLC IMER ED是一种灵敏且可靠的测定ACh和Ch的方法 ,和微透析技术相结合可以动态监测清醒自由活动大鼠脑内细胞外液中ACh和Ch的水平。

Fixation of Multiple Metals in Contaminated Soil by Different Passivators

The effects of 4 passivators, zeolite, lime, red mud and peanut shell biochar, on the fixation of Cd, Pb, Cu and Zn in acidic multi-metal contaminated soils were studied by passivator culture experiment in order to screen out the passivator with better fixation effects. The results showed that the soil pH values of zeolite, lime, red mud and peanut shell biochar increased significantly by 0.511.02, 0.821.29, 0.720.89 and 0.300.35 respectively. The effects of 4 passivators on the fixation of Cd and Zn in soil are lime>red mud>zeolite>peanut shell biochar. The order of effects on the fixation of Pb is red mud>lime>zeolite>peanut shell biochar. The order of the fixation effects of Cu is red mud>lime>peanut shell carbon>zeolite. The contents of Cd, Pb, Cu and Zn in the extractable state of CaCl2 decreased with the increase in the dosage of 4 passivators. Lime and red mud showed good fixation effects on Cd, Pb, Cu and Zn. The contents of Cd, Pb, Cu and Zn in the extractable state of CaCl2 at the low dosage(2.5 g/kg) of lime and red mud decreased by 41%, 84%, 76% and 83% respectively. Soil pH value was negatively correlated with CaCl2-Cd, Pb, Cu and Zn(P<0.01). Lime and red mud had significant fixation effects on Cd, Pb, Cu and Zn in acidic multi-metal contaminated soils at low application dosages.

Microbial processes and factors controlling their activities in alkaline lakes of the Mongolian plateau

A striking feature of the Mongolian plateau is the wide range of air temperatures during a year, -30 to 30~C. High summer temperatures, atmospheric weathering and the arid climate lead to formation of numerous alkaline soda lakes that are covered by ice during 6-7 months per year. During the study period, the lakes had pH values between 8.1 to 10.4 and salinity between 1.8 and 360 g/L. According to chemical composition, the lakes belong to sodium carbonate, sodium chloride-carbonate and sodium sulfate-carbonate types. This paper presents the data on the water chemical composition, results of the determination of the rates of microbial processes in microbial mats and sediments in the lakes studied, and the results of a Principal Component Analysis of environmental variables and microbial activity data. Temperature was the most important factor that influenced both chemical composition and microbial activity, pH and salinity are also important factors for the microbial processes. Dark CO2 fixation is impacted mostly by salinity and the chemical composition of the lake water. Total photosynthesis and sulfate-reduction are impacted mostly by pH. Photosynthesis is the dominant process of primary production, but the highest rate （386 mg C/（L.d）） determined in the lakes studied were 2-3 times lower than in microbial mats of lakes located in tropical zones. This can be explained by the relatively short warm period that lasts only 3-4 months per year. The highest measured rate of dark CO2 assimilation （59.8 mg C/（L·d）） was much lower than photosynthesis. The highest rate of sulfate reduction was 60 mg S/（L·d）, while that of methanogenesis was 75.6 μL CH4/（L·d） in the alkaline lakes of Mongolian plateau. The rate of organic matter consumption during sulfate reduction was 3-4 orders of magnitude higher than that associated with methanogenesis.

Study on treatment of acidic black 10B dye wastewater by chemical oxidation and adsorption of activated carbon fixed bed

Acidic black 10B dye wastewater was treated by chemical oxidation and adsorption of activated carbon fixed bed and all kinds of influential factors of removal CODcr were discussed. When the initial concentration of the dye was 150 mg/L, CODer was 432 mg/L and chrome was 2800 times, the appropriate conditions determined by the experiment were as follows： r（NaC10）--4.84 g/L, 25 min, pH=6, height of activated carbon fixed bed was 10 cm. Under these conditions, the decolorizing rate can come up to about 100% and total removed rate of CODer reached at 89.6%. Comparison of UV-Vis adsorption spectrums before and after treatment showed that decomposition effects of chemical oxidation and adsorption of activated carbon fixed bed on acidic black 10B dye wastewater were satisfactory.

Studies of Photocatalytic Kinetics on the Degradation of Bisphenol A （BPA） by Immobilized ZnO Nanoparticles in Aerated Photoreactors

The photocatalytic kinetics of BPA （4, 4＇-isopropylidenediphenol）, a representative endocrine disruptor, was explored using immobilized ZnO nanoparticles as a photocatalyst in a laboratory scale photocatalytic reactor. The conditions of photocatalytic degradation were optimized. Direct photocatalytic degradation of BPA was undertaken in an aqueous solution containing ZnO nanoparticles under the optimized experimental conditions. The effects of various factors, such as initial BPA concentrations, initial pH values and various anions （CI, NO3, COa2, SO42-, HCO3＂） were investigated. In the case of the nanoparticles derived films, the photocatalytic efficiency was found not to be remarkably related with the calcination temperature employed in the coating process. Screen-printed ZnO nanoparticles films obtained in the optimal processing conditions showed that the photocatalytic activity is comparable to ZnO nanoparticles in aqueous suspensions. Over 90% degradation efficiency of BPA was achieved under the optimum conditions. The degradation rates in all photocatalytic experiments were linear with the degradation efficiencies of BPA by regression analysis （r ≥ 0.99）. The results showed that the degradation kinetics of BPA in the reactor with immobilized nano-ZnO film as photocatalyst was in agreement with a pseudo-first order rate law.

Recyclable cobalt-molybdenum bimetallic carbide modified separator boosts the polysulfide adsorption-catalysis of lithium sulfur battery

The polysulfide shuttling and sluggish redox kinetics,due to the notorious adsorption-catalysis underperformance,are the ultimate obstacles of the practical application of lithium-sulfur(Li-S)batteries.Conventional carbon-based and transition metal compound-based material solutions generally suffer from poor catalysis and adsorption,respectively,despite the performance gain in terms of the other.Herein,we have enhanced polysulfide adsorptioncatalytic capability and protected the Li anode using a complementary bimetallic carbide electrocatalyst,Co3 Mo3 C,modified commercial separator.With this demonstration,the potentials of bimetal compounds,which have been well recognized in other environmental catalysis,are also extended to Li-S batteries.Coupled with this modified separator,a simple cathode(S/Super P composite)can deliver high sulfur utilization,high rate performance,and excellent cycle stability with a low capacity decay rate of^0.034%per cycle at 1 C up to1000 cycles.Even at a high S-loading of 8.0 mg cm^-2 with electrolyte/sulfur ratio=6 m L g^-1,the cathode still exhibits high areal capacity of^6.8 m A h cm^-2.The experimental analysis and the first-principles calculations proved that the bimetallic carbide Co3 Mo3 C provides more binding sites for adsorbing polysulfides and catalyzing the multiphase conversion of sulfur/polysulfide/sulfide than monometallic carbide Mo2 C.Moreover,the modified separator can be reutilized with comparable electrochemical performance.We also showed other bimetallic carbides with similar catalytic effects on Li-S batteries and this material family has great promise indifferent energy electrocatalytic systems.

Photochemical fixation and reduction of sulfur dioxide to sulfide by tetraphenylporphyrin magnesium:Spectroscopic and kinetic studies

The photochemical reaction of sulfur dioxide （802） with tetraphenylporphyrin magnesium （MgTPP） has been investigated in dichloromethane （CH2C12） solution at room temperature with illumination by visible light. Conventional fluorescence, UV-vis, and MS spectral analyses showed that under these conditions, SO2 was initially photochemically fixed by MgTPP to form a 1：1 molecular adduct. On continued irradiation and maintaining the flow of SO2, MS and XRD results showed that MgTPP is re- markably effective in the photochemical reduction of SO2 to sulfide （S2 ）. The kinetics of the photochemical reaction of MgTPP with SO2 was studied in a SO2-saturated solution. Under irradiation, the reaction follows pseudo first order kinetics for MgTPP, having a half-life decreasing from 106 to 57 min as the illumination intensity is increased from 350 to 600 Lm. This investigation of the photochemical fixation and reduction of SO2 by MgTPP is of key interest in elucidating fundamental pho- tochemical reaction mechanisms associated with porphyrins in the presence of SO2; furthermore, the analysis of the photo- chemical reaction may offer new opportunities for the fixation and reduction of SO2 to less harmful species.

The preparation of supported ionic liquids (SILs) and their application in rare metals separation

This review summarizes the preparation methods of support ionic liquids （SILs） and their applications in rare metals separation The rare metals separation includes the recovery of high value metal ions and the removal of heavy metal ions from wastewater. SILs can be used as a kind of highly efficient multifunctional separation materials. The preparation methods of SILs include chemical immobilization technique in which ILs moieties are supported on solid supports via covalent bonds and physical immobilization techniques in which ILs are immobilized on solid supports via physical method such as simple im- pregnation, sol-gel method. According to the difference of solid supports, this review summarizes the application of polymer supported ionic liquids （P-SILs）, silica based material supported ionic liquids （SM-SILs） and membrane supported ionic liq- uids （M-SILs） in rare metals separation, P-SILs and SM-SILs prepared by chemical method with N-methylimidazolium group can be used as highly efficient anion exchangers with high thermal stability and good chemical stability for adsorption of Cr（Ⅵ）, Re（Ⅶ）, Ce（Ⅳ）. P-SILs prepared via simple impregnation afforded IL functionalized solvent impregnated resins （SIRs） which showed high separation efficiency and selectivity in the separation of rare earths（Ⅲ） （REs（Ⅲ））. SM-SILs prepared via sol-gel method with IL doped in the support as porogens or extractant show high removal efficiencies and excellent stability for the separation of RE（Ⅲ）, Cr（Ⅲ） and Cr（Ⅵ）. M-SILs with IL as plasticizer or carrier show improved stability, high perme- ability coefficient and good selectivity for Cr（VI） transport. Different supports and different supporting methods were suffi- ciently compared. Based on the different practical application, different forms of SILs can be prepared for separation of rare metals with high separation efficiency and selectivity.