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141.
142.
Speed of sound and density of 1-propanol + heavy water were measured in the whole concentration range at temperatures from 293 to 313 K. Isentropic compressibility was calculated from the Laplace formula. The partial molar volume of 1-propanol reaches a minimum at the mole fraction of 1-propanol x
1 0.03. At the same concentration, the compressibility isotherms intersect one another. These features of the investigated system are similar to those of 1-propanol + H2O, that points to essential similarity of the two mixtures. A clathrate-like structure was suggested to explain the experimental results for dilute solutions of the alcohol. Somewhat more pronounced hydrophobic hydration in D2O than in H2O is manifested by an effect similar to that resulting from the elongation of the alcohol molecule. 相似文献
143.
144.
The polystyrene supported phenylalanine Schiff base complex of Mn(Ⅱ)(PS-Sal-Phe-Mn)was prepared with chloromethylated styrene polymer beads, 2,4-dihydroxybenzaldehyde,L-phenylalanine and manganese(Ⅱ)acetate tetrahyrate., The polymeric ligand and the complex were characterized by FT-IR,, small area X-ray photoelectron spectroscopy(XPS), and ICP-AES. In the presence of the manganese complex, cyclohexene(1)was effectively oxidized by molecular oxygen without reductant. The major products of the reaction were 2-cyclohexen-1-ol(2),2-cyclohexen-1-one(3)and 2-cyclohexen-1- hydroperoxide(4), which was different with typical oxidation of cyclohexene. The influence of reaction temperature and additive for oxidation had been studied. The selectivity of 2-cyclohexen-l-hydroperoxide varied with reaction time and different additives. The mechanism of cyclohexene oxidation had also been discussed. 相似文献
145.
《Surface and interface analysis : SIA》2005,37(5):495-498
The oxidation of iron (Fe) by water (D2O) vapour at low pressures and room temperature was investigated using time‐of‐flight (ToF) SIMS. The results supported those found previously using XPS and the QUASES? program in that a duplex oxide structure was found containing a thin outer surface hydroxide (Fe(OD)2) layer over an inner oxide (FeO) layer. The extraordinary depth resolution of the ToF‐SIMS profiles assisted in identifying the two phases; this resolution was achieved by compensation for surface roughness. A substantial concentration of deuterium was found in the subsurface oxide layer. This observation confirmed previous assessments that the formation of FeO was from the reaction of Fe(OD)2 with outward‐diffusing Fe, leaving deuterium as a reaction product. Copyright © 2005 John Wiley & Sons, Ltd. 相似文献
146.
制备了一系列V,Ag,Ni原子比不同的三元氧化物,应用TPD-MS技术研究了样品表面氧的性质,并测定了甲苯选择性氧化生成苯甲醛的催化活性。实验结果表明,样品表面存在有多种吸附的氧物种。在脱附温度<900℃:当Ni含量对Ag(或V)的原子比为0.25或0.50时,仅在低温处出现有表面的O^-和O^2^-两种氧物种的脱附峰;当Ni含量对Ag(或V)的原子比增高到>0.75时,除有表面的O^-和O^2^ 相似文献
147.
A. V. Kazakova N. D. Kushch L. I. Buravov E. B. Yagubskii S. V. Simonov L. V. Zorina S. S. Khasanov R. P. Shibaeva E. Canadell J. Yamada M. Umemiya 《Russian Chemical Bulletin》2007,56(1):49-55
New radical cation salts based on 2,5-bis(1,3-dithian-2-ylidene)-1,3,4,6-tetrathiapentalene (BDA-TTP) with copper(II) metal complex anions, β-(BDA-TTP)4Cu2Cl6 and (BDA-TTP)2CuCl4, were synthesized and structurally characterized. Single crystals were prepared by electrochemical oxidation of BDA-TTP under
galvanostatic conditions. X-ray diffraction study demonstrated that the salts have a layered structure, in which the conducting
BDA-TTP layers alternate with the [Cu2Cl6]2− or [CuCl4]2− anions. Both salts show the semiconductor-type temperature dependence of the conductivity.
Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 1, pp. 48–54, January, 2007. 相似文献
148.
纳米TiO2膜用于光催化氧化测定化学需氧量的研究 总被引:4,自引:0,他引:4
A photocatalytic oxidation method for determination of chemical oxygen demand (COD) using nano-TiO2 film, based on the use of a nano-TiO2-Ce(SO4)2 system and electrochemical detection, was proposed. The technique was originated from the direct determination of the Ce(Ⅲ) concentration change resulting from photocatalytic oxidation of organic compounds. Ce(Ⅲ), which was produced by photocatalytic reduction of Ce(SO4)2, could be measured at a multi-walled carbon nanotubes (MWNT) chemically modified electrode (CME). The COD values by this method were calculated from the differential pulse voltammetry (DPV) current of Ce(Ⅲ) at the CME. Under the optimal operation conditions, the detection limit of 0.5 mg·L^-1 COD with the linear range of 1-600 mg·L^-1 was achieved. This method was also applied to determination of various COD of ground water and wastewater samples. The resuits were in good agreement with those from the conventional COD methods, i.e., permanganate and dichromate ones. 相似文献
149.
Zhuang Hong Cheng Tiexin Bi Yingli Zhou Guangdong Zhen Kaiji 《Reaction Kinetics and Catalysis Letters》2004,81(1):13-20
Factors (reaction temperature, reaction time, flow rate of oxygen, amount of catalyst, etc.) influencing the catalytic properties of Co3O4/SiO2catalyst in the oxidation octadecan-1-ol to octadecanoic acid were investigated. The catalysts were characterized by means of XRD, FT-IR and N2-adsorption. The experimental results indicate that under the optimal condition the selectivity to octadecanoic acid reached 97.5 % over 5 % Co3O4/SiO2 catalyst.This revised version was published online in December 2005 with corrections to the Cover Date. 相似文献
150.
Sol-gel Cu//MgOSiO2 catalysts were prepared gelling tetraethoxysilane (TEOS), magnesium ethoxide and copper acetylacetonate at pH 3 and pH 9. The catalysts shown specific surface areas ca. 500 m2/g and 140 m2/g for pH 9 and pH 3 preparations respectively. Si(OH) and Si(OH)2 hydroxy groups were observed by MAS-RMN spectroscopy in both preparations. CO2-TPD and NH3-TPD desorption thermograms showed that acid and basic sites were formed on the catalysts surface. It has been found that the catalysts having the highest density of basic sites were the catalysts showing the highest activity for the CO oxidation. It is proposed that the catalytic activity depends of the relative Cu=1/Cu=2 stability given by the support acidity. 相似文献