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61.
现场表面拉曼光谱研究Fe-Mo合金诱导共沉积 总被引:1,自引:0,他引:1
现场表面拉曼光谱结果显示,在0.2mol·L-1Na2MoO4,pH=4.0的溶液中,电位正于0.5V(vsSCE)时只观察到多钼酸盐的拉曼峰(940、880和450cm-1).负于-0.5V时,出现中心位于730cm-1的宽峰.同时电极表面有蓝色膜生成.表明混合氧化态(MO(Ⅳ),MO(Ⅴ))氧化膜的形成.730cm-1的峰在-1.9V时仍然存在,说明氧化膜没有被进一步还原.在钼酸钠溶液中同时含有0.1mol·L-1FeSO4和0.2mol·L-1柠檬酸时,中间态氧化膜的拉曼峰的中心移到740cm-1.且峰强度随着电位从-1.3V负移到-1.9V而逐渐减弱并最终消失.电极表面沉积层呈银白色,说明由于Fe2 的存在,钼的中间态氧化膜的结构发生了变化,能够被进一步还原形成Fe-Mo合金,表现出诱导共沉积的特征. 相似文献
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The growth of cobalt hexacyanoferrate (CoHCF) films on bare and Au-colloid-modified electrodes in nitrate or sulfate solutions was monitored by electrochemical quartz crystal microbalance. The average efficiency of CoHCF film growth for Au colloid modified electrodes is 23 and 12 ng cm(-2) s(-1) in KNO3 and K2SO4 solutions, respectively, while those values for the bare gold electrode are 15 and 9 ng cm(-2) s(-1), respectively. In K2SO4 solution, the apparent molar masses for the Au-colloid-modified electrode at lower and higher potential is 58.4 and 37.3 g mol(-1), respectively, which is larger than those for the bare gold electrode (51.7 and 26.3 g mol(-1), respectively). The respective results were also obtained in KNO3 solution. Furthermore, the difference of the apparent molar masses at lower and higher potential for Au-colloid-modified electrodes is smaller than that for bare gold electrodes in the same electrolyte. Additionally, the mechanism of charge propagation is dependent on different anions in electrolyte solutions at higher potentials where the second redox reaction of CoHCF occurs. Therefore, the existence of Au colloids can accelerate CoHCF film growth and weaken the effect of anions on mass transport. 相似文献
64.
[reaction: see text] A 30-member library of small molecules based on the vinyl sulfone scaffold was prepared on rink amide resin, using solid phase-based reactions such as oxidation and Horner-Wadsworth-Emmons reaction. The library was designed such that three points of diversity were readily introduced in the library to accommodate the S(1)', S(1), and S(2) binding pockets of different cysteine proteases, making the strategy suitable for high-throughput generation of potential cysteine protease inhibitors. 相似文献
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Direct electrochemical and electrocatalytic behavior of hemoglobin (Hb) immobilized on glass carbon electrode (GCE) containing gelatine (Gel) films was investigated. The characteristics of Hb/Gel film modified GC electrode were performed by using SEM microscopy, UV-vis spectroscopy and electrochemical methods. The immobilized Hb showed a couple of quasi-reversible redox peak with a formal potential of −0.38 V (versus SCE) in 0.1 M pH 7.0 PBS. The formal potential changed linearly from pH 4.03 to 8.41 with a slope value of −52.0 mV pH−1, which suggested that a proton transfer was accompanied with each electron transfer (ET) in the electrochemical reaction. The Hb/gelatine/GCE displayed a rapid amperometric response to the reduction of H2O2 and nitrite. 相似文献
67.
Dachun Yao 《Analytica chimica acta》2003,478(1):23-30
A new detection system based on microdialysis sampling and chemiluminescence (CL) reaction was developed for in vivo monitoring of uric acid (UA) with high sensitivity, selectivity and accuracy. The uric acid is indirectly monitored by CL detection of enzymatic reaction product formation (H2O2), catalyzed by Uricase. A microprobe was modified and coated with immobilized enzyme through a Streptavidin-biotin mediated linker by using a chitosan support membrane, polyurethane trapped ferrocene film is employed to protect the probe surface and diminish the interference from reductant molecules, which often are present in the blood (e.g. ascorbic acid). The earlier mentioned probe and the constructed sensor can detect uric acid in the range of 0.01-1 mM with detection limit (3σ) of 5 μM. Finally, the system is used to monitor uric acid (UA) variation through an acute myocardial infarction (AMI) model. Following AMI-induced oxidative stress, the UA level decreases continuously, thus suggesting that UA plays a protective role as a substitute antioxidant. Furthermore, the in vivo monitoring results show good agreement with those obtained by a standard method, and the procedure is recommended for in vivo and real time monitoring of UA. In addition, the proposed method can be more accurate since the UA may be potentially oxidized by in vitro exposure to oxygen in the presence of a catalyst. 相似文献
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Nb6.74Ta5.26S4 has been prepared by high temperature techniques. The crystal structure has been determined from single crystal X-ray diffraction data (R/Rw = 0.0588/0.0655). The compound crystallizes in the orthorhombic space group Pnma with unit cell dimensions a = 959.11 (26) pm, b = 336.37 (10) pm, and c = 3282.51 (74) pm. The orthorhombic cell contains four formula units. Its structure is similar to that of Nb-rich sulfides, rather than to that of Ta-rich sulfides. The metal coordinations are capped distorted cubic prisms and pentagonal prisms while the coordinations of sulfur are capped trigonal prisms. 相似文献
70.
Xin Sheng Li Yao Jun Zhang Qin Xin Chun Xin Ji Yan Fen Miao Li Wang 《Reaction Kinetics and Catalysis Letters》1996,57(1):177-182
Volumetric H2-uptake measurements on an Mo2N (79 m2g–1) sample reduced at 673 K have been carried out and the uptake isotherms in the temperature range of 308–623 K have been determined. Both the total and reversible hydrogen uptake increased with the uptake temperature. The irreversible hydrogen uptake increased abruptly when the uptake temperature was raised up to 423 K. The maximum of irreversible hydrogen uptake was measured at 473 K. The HIR/Mo ratio calculated from the uptakes obtained in the temperature range of 308–623 K varies in the range of 0.0010–0.0202. One possible mechanism for hydrogen adsorption is proposed to be heterolytic dissociation on Mo-N paris, in which the molybdenum atoms are in unsaturated coordination. 相似文献