Adsorption separation performance of H2/CH4 on ETS-4 by concentration pulse chromatography

To exploit an effective adsorbent to separate hydrogen and methane, microporous titanium silicate molecular sieve NaETS-4 was synthesized and modified by strontium. The adsorption characteristics and diffusion behaviors of the prepared titanosilicate molecular sieve were studied by concentration pulse chromatography. And the effects of ion-exchange and dehydration temperature on adsorbent structure and gas diffusion were also discussed. The results showed that the thermal stability and Henry＇s Law constants were enhanced and micropore diffusivity decreased after exchanging Na＋ with Sr2＋. With the increase of dehydration temperature, Henry＇s Law constant and micropore diffusivity of CI-I4 decreased in both NaETS-4 and SrETS-4. While for 1-12 in SrETS-4, the increase of Henry＇s Law constant and the decrease of diffusion rate can be attributed to the shrinks of pore diameter resulting from the relocation of Sr2＋. Correspondingly, the kinetic selectivity of H2/CH4 reached 8.91 indicating its potentiality in separating H2 and CH4.     

Preparation and characterization of Ti0.7Sn0.3O2 as catalyst support for oxygen reduction reaction

Sn-doped TiO_2 nanoparticles with high surface area of 125.7 m~2·g~(-1) are synthesized via a simple one-step hydrothermai method and explored as the cathode catalyst support for proton exchange membrane fuel cells.The synthesized support materials are studied by X-ray diffraction analysis,energy dispersive X-ray spectroscopy and transmission electron microscopy.It is found that the conductivity has been greatly improved by the addition of 30 mol%Sn and Pt nanoparticles are well dispersed on Ti_(0.7)Sn_(0.3)O_2 support with an average size of 2.44 run.Electrochemical studies show that the Ti_(0.7)Sn_(0.3)O_2 nanoparticles have excellent electrochemical stability under a high potential compared to Vulcan XC-72.The as-synthesized Pt/Ti_(0.7)Sn_(0.3)O_2 exhibits high and stable electrocatalytic activity for the oxygen reduction reaction.The Pt/Ti_(0.7)Sn_(0.3)O_2 catalyst reserves most of its electrochemically active surface area(ECA),and its half wave potential difference is 11 mV,which is lower than that of Pt/XC-72(36 mV) under 10 h potential hold at 1.4 V vs.NHE.In addition,the ECA degradation of Pt/Ti_(0.7)Sn_(0.3)O_2is 1.9 times lower than commercial Pt/XC-72 under 500 potential cycles between 0.6 V and 1.2 V vs.NHE.Therefore,the as synthesized Pt/Ti_(0.7)Sn_(0.3)O_2 can be considered as a promising alternative cathode,catalyst for proton exchange membrane fuel cells.     

黄油中8种类固醇激素的液相色谱/串联质谱检测

建立了黄油中雌酮、α-雌二醇、β-雌二醇、雌三醇、睾酮、表睾酮、孕酮和丙酸睾酮8种类固醇激素的凝胶渗透色谱(GPC)-液相色谱/串联质谱(LC-MS/MS)检测方法。样品用乙酸乙酯-环己烷(1∶1,V/V)提取,提取液经GPC柱净化除脂,GPC浓缩液采用C18色谱柱(100 mm×2.0 mm i.d.,3.0μm)分离,以乙腈和水为流动相进行梯度洗脱,电喷雾电离多反应监测模式进行定性和定量分析。8种类固醇激素以基质匹配外标法定量,药物在1.0~20.0μg/kg线性范围内相关系数(r)均大于0.999;方法检出限(S/N=3)为0.04~0.30μg/kg,定量限LOQs(S/N=10)为1.0μg/kg;添加水平为1.0,2.0,4.0μg/kg时,回收率范围在64.1%~110%之间;相对标准偏差(RSD)小于11%。结果表明,本方法准确、可靠,满足黄油中8种类固醇激素的检测分析要求。     

Synthesis,Crystal Structure and MMCT Property of a New Mixed-valence Cyanide-bridged Binuclear Complex

A new mixed-valence cyanide-bridged complex, Br3Fe(μ-NC)RuBr(dppm)2(dppm = bis(diphenylphosphino)methane), was obtained through the reaction between trans-(dppm)2ClRuCN and FeBr3. Its crystal structure was characterized. Electronic absorption spectra indicate the existence of metal-to-metal charge transfer(MMCT) and this complex is Class Ⅱ mixed valence complexes according to the classification of Robin and Day. Magnetic analysis shows it is paramagnetic.     

Synthesis and Antibacterial Activity of Novel 5,5′-(Pyridine-2,6-Diyl)bis(4-Arylideneamino-3-Mercapto-1,2,4-Triazole)-Related Derivatives

The reaction of 5,5′-(pyridine-2,6-diyl)bis(4-amino-3-mercapto-1,2,4-triazole) with various aromatic aldehydes in acetic acid yielded the corresponding 5,5′-(pyridine-2,6-diyl)bis(4-arylideneamino-3-mercapto-1,2,4-triazole) derivatives. The structures of the synthesized compounds as well as their intermediates were confirmed by elemental analysis, infrared spectra, ¹H NMR spectra and mass spectra studies. All the synthesized title compounds were screened for their antibacterial activities, and the preliminary results revealed that some of them showed good activities against Escherichia coli and Pseudomonas aeruginosa.     

Enhanced Expression of GCRV VP6 in CIK Cells by Relative Sequence Optimization

Efficient expression of target protein is one of strategies for gene therapy or vaccine design. Many studies showed that codon optimization could enhance the expression of target proteins. In this paper, a target sequence of about 1.26 kb encoding the major capsid protein VP6 of grass carp reovirus (GCRV) and an optimized counterpart were synthesized and inserted into vectors for expressing VP6. The final constructs (named as pcDV6G and pcDV6YG) were transfected in Ctenopharyngodon idellus kidney (CIK) cells. The fluorescence analysis and the Western blot results showed that the gene fragment was transfected and expressed in CIK cells successfully. Although the qRT-PCR results showed no difference at the messenger RNA (mRNA) levels between the different versions of vp6 in the indicated stages, the enzyme-linked immunosorbent assay (ELISA) results showed that the protein level of VP6 expressed by pcDV6YG was higher than that by pcDV6G in the indicated hours. Taken together, these results suggest that the enhanced expression of GCRV VP6 in CIK cells by relative sequence optimization may be a good choice for making DNA vaccine against GCRV.     

pH-responsive pseudorotaxane between comblike PEO-grafted triblock polymer and α-cyclodextrin

The pH-responsive inclusion complexation of comblike triblock polymer, P2VP-b-PPEOMA-b-P2VP, with α-cyclodextrin (α-CD) was studied. The triblock polymer was prepared by reversible addition–fragmentation chain transfer polymerization (RAFT) and formed inclusion complexes (ICs) after selective threading of the PEO segment of the triblock polymer through the cavities of α-CD units. For comparison, PPEOMA homopolymer was prepared, and the inclusion complexation with α-CD was also studied. The formed ICs were characterized by XRD and ¹H NMR. The results revealed that P2VP-b-PPEOMA-b-P2VP can form ICs with α-CD even when forming micelles, and the introduction of P2VP had a great influence on the solution property and the stoichiometry of EO to CD of the inclusion complexes depending on the concentration and the pH of the solution.     

表面增强拉曼光谱在食品安全分析中的应用

拉曼光谱技术具有样品用量少、快速高效、无损分析等特点,表面增强拉曼光谱克服了常规拉曼光谱灵敏度低的缺点,可以获得更多物质结构信息,在现场快速筛查、检测和鉴别农兽残、限用或禁用添加剂分析检测中具有广阔的应用前景。本文综述了表面增强拉曼光谱在食品中农药残留、兽药残留和限/禁用添加剂检测中的研究进展,并展望了其发展前景。     

豆芽中甲硝唑、多菌灵、赤霉素、6-苄基腺嘌呤、2,4-二氯苯氧乙酸的定量检测

本文建立了快速筛查豆芽中常见添加物甲硝唑、多菌灵、赤霉素、6-苄基腺嘌呤和2,4-二氯苯氧乙酸的液相色谱定量方法。回收率为79%～96.6%,定量限在20～200μg/kg。对市场随机抽查64份豆芽样品检测发现,高达32份样品中含有1种以上添加物,主要是多菌灵、6-苄基腺嘌呤和2,4-二氯苯氧乙酸。     

Nitrobenzene degradation by micro-sized iron and electron efficiency evaluation

The effect of pH, temperature, zero-valent iron (ZVI) dosage and reaction duration on nitrobenzene (NB) degradation by micro-sized ZVI was investigated in batch experiments and the electron efficiency (EE) was evaluated at constant pH. The experimental results showed that the reaction rate constant attained 0.616 min^?1, which was far higher than reported in previous studies. The decrease in pH and increase in temperature of the reaction bath promoted the reaction kinetics. ZVI dosage and reaction duration were two key factors affecting NB reduction and EE. A lower ZVI dosage and a slightly longer reaction duration could afford an optimised EE and optimum NB removal. A prolonged reaction or too high a ZVI dosage resulted in increased ZVI waste.