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931.
932.
Saulius Martusevi
ius Gediminas Niaura Zita Talaikyt Valdemaras Razumas 《Vibrational Spectroscopy》1996,10(2)
The adsorption of
-histidine on a copper electrode from H2O- and D2O-based solutions is studied by means of surface-enhanced Raman scattering (SERS) spectroscopy. Different adsorption states of histidine are observed depending upon pH, potential, and the presence of the SO2−4 and Cl− ions. In acidic solutions of pH 1.2 the imidazole ring of the adsorbed histidine remains protonated and is not involved in the chemical coordination with the surface. The SO2−4 and Cl− ions compete with histidine for the adsorption sites. In solutions of pH 3.1 three different adsorption states of histidine are observed depending on the potential. Histidine adsorbs with the protonated imidazole ring oriented mainly perpendicularly to the surface at potentials more positive than −0.2 V. Transformation of that adsorption state occurs at more negative potentials. As this takes place, histidine adsorbs through the α-NH2 group and the neutral imidazole ring. The Cl− ions cause the protonation and detachment of the α-NH2 group from the surface and the formation of the ion pair NH+3 … Cl− can be observed. In the neutral solution of pH 7.0 histidine adsorbs through the deprotonated nitrogen atom of the imidazole ring and the α-COO− group at E ≥ −0.2 V. However, this adsorption state is transformed into the adsorption state in which the α-NH2 group and/or neutral imidazole ring participate in the anchoring of histidine to the surface, once the potential becomes more negative. In alkaline solutions of pH 11.9 histidine is adsorbed on the copper surface through the neutral imidazole ring. 相似文献
934.
Error of DIAL-measured Ozone Concentration and a Three-Wavelength Inversion Technique 总被引:1,自引:0,他引:1
邱金桓 《中国科学B辑(英文版)》1993,(11)
Sensitivity of the error in the stratospheric ozone concentration measured by DIAL to the scattering property of the stratospheric aerosol is studied through both theoretical analysis and numerical experiment in this paper, and based on the sensitivity, a three-wavelength lidar inversion technique is proposed for a simultaneous determination of ozone concentration profile, aerosol backscatter coefficient profile and its size distribution in the stratosphere. It is found from the sensitivity study that there is a considerable effect of the stratospheric aerosol on accuracy of the ozone concentration solution. If the aerosol scattering is neglected, a large error of the solution can be obtained, especially when there is the stratospheric volcanic cloud, the error can be up to 100%. According to numerical experiments, a great improvement of the ozone concentration solution is obtained by using the present three-wavelenght inversion method. 相似文献
935.
磷酸三丁酯萃取原子吸收光谱法测定微量Cr(Ⅲ)和Cr(Ⅵ) 总被引:2,自引:0,他引:2
常用的 APDC-MIBK 和 DDTC-MIBK 萃取原子吸收法一般只能测至十几个ppb 浓度的铬,且需在较高温度下进行萃取.本文报道一种用磷酸三丁酯(TBP)萃取原子吸收光谱法测定微量 Cr(Ⅲ)和 Cr(Ⅵ)的方法.实验表明,Cr_2O_7在盐酸介质中可与 TBP 形成 Cr(Ⅵ)-TBP-Cl-溶剂化合物,借此可测定0-0.25μg·ml~(-1)浓度范围内的 Cr(Ⅵ).若用 KMnO_4将平行试样中的 Cr(Ⅲ)氧化为 Cr(Ⅵ),测得总铬量,通过差减法即可算出Cr(Ⅲ)的含量.本法灵敏度高,准确度好. 相似文献
936.
原子吸收法测定中药脑心通中微量和宏量元素的含量 总被引:1,自引:0,他引:1
采用原子吸收分光光度法测定了脑心通胶囊中钠、钾、钙、镁、铁、铬、锰、镍、镉、铜、锌11种元素的含量。结果表明,脑心通胶囊中含有较丰富的微量元素,为探讨中药脑心通中微量元素与治疗心脑血管疾病的关系提供了有用的数据。 相似文献
937.
R. Bruce King 《Theoretical chemistry accounts》1980,56(4):269-296
The following procedure is described for investigating the qualitative dynamics of simple chemical systems: 1) A so-called influence diagram is generated representing the relationships between the reference reactants (phase-determining intermediates); 2) This influence diagram is used to generate a truth table indicating possible transitions between state vectors representing the signs of the time derivatives of of the reference reactant concentrations; 3) The truth table is used to determine a state transition diagram representing the flow topology around unstable equilibrium points; 4) The characteristic equation of the adjacency matrix of the influence diagram is solved in order to determine the presence of such unstable equilibrium points. The two types of qualitative dynamics possible for chemical systems containing two reference reactants and one feedback circuit are bifurcation between two attracting regions (bistability) and limit cycle oscillation. However, in two reference reactant systems oscillation requires an additional self-activating loop to generate the unstable equilibrium point required for its realization. Bistability and limit cycle oscillation are also two of the possible types of qualitative dynamics for chemical systems containing three reference reactants. However, chemical systems with three reference reactants and two or more feedback circuits can also contain interlocking limit cycles, which can lead to toroidal oscillations or chaos. The influence diagrams are given for the systems exhibiting these various types of dynamic behavior along with a summary of the important properties of all 729 possible influences for simple chemical systems containing three reference reactants. 相似文献
939.
Hans‐Peter Kormann Günter Schmid Katrin Pelzer K. Philippot Bruno Chaudret 《无机化学与普通化学杂志》2004,630(12):1913-1918
Nanoporous alumina membranes, loaded with palladium and ruthenium nanoparticles of various size, were used for gas phase hydrogenation of 1, 3‐butadiene and for oxidation of carbon monoxide, respectively. Those membranes contain 109 ‐ 1011 pores per cm2, all running perpendicular to the surface. Membrane discs of 20 mm in diameter and only 60 μm thick, incorporated in a reactor in which the reactants can be pumped in a closed circuit through the pores, turned out to very actively catalyze hydrogenation of butadiene (Pd) and oxidation of CO (Ru). The activity of the Pd catalysts depends characteristically on the particles size, the gas flow, and of the educts ratio. As could be expected, larger particles are less active than smaller ones, whereas increasing gas flows in case of hydrogenation accelerates the reactions. Excessive hydrogen reduces selectivity with respect to the various butenes, but favours formation of butane. 相似文献
940.
The rhodium-phosphine complex catalyst Rh(CO)(acac)(PPh3)(Ⅰ) for 1-hexene hydroformylation was studied under the following reaction conditions: CO/H2=1(mole rate), pressure 1.0 MPa, temperature 25-120℃, by using the pressurized in-situ 1H NMR technique. Experimental results indicated that the formation of a rhodium hydride complex from (Ⅰ) began at room temperature and its amount increased with increasing of reaction temperature. This intermediate complex began to decompose at 100℃ and disapeared completely at 120℃. The intensity change of the proton signal was parallel to catalytical activity in hydroformylation of olefins. Under pure CO pressure the proton signal of Ph-H bond was not observed. There was a 0.2 ppm difference in proton chemical shifts of Rh-H bond under pure H2 pressure and under H2+CO pressure. The results showed that the rhodium-hydride carbonyl complex is the active intermediate in the industrial hydroformylation process. 相似文献