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91.
M. R. Yaftian M. Burgard D. Matt C. Wieser C. Dieleman 《Journal of inclusion phenomena and macrocyclic chemistry》1997,27(2):127-140
The complexing, extracting and mobile carrier properties of the tetra(phosphine oxide)-calix[4]arene 1 and the hybrid diamide-di(phosphine oxide)-calix[4]arene 2 were studied. Both ligands give 1 : 1 complexes with alkali cations in THF as shown by the picrate method. 1H NMR experiments were run to follow encapsulation of sodium and potassium cations. The corresponding spectra indicate C2-symmetrical structure. The observed extraction orders of the alkali picrates were as follows K+>Rb+>Li+>Cs+>Na+ for 1 and Li+>Na+>K+>Rb++ for 2. Transport kinetics was analysed by means of a model which assumes pure diffusion and which allows the evaluation of mass transfer coefficients in all systems. These coefficients and their influences on the transport rate are discussed in terms of size of the transporting species in the liquid membrane. 相似文献
92.
导电氧化物电极上丁酸丁酯电化学合成的研究 总被引:4,自引:0,他引:4
本文研究了某些氧化物电极在不同条件下对丁醇电解直接合成丁酸丁酯的影响,并测定了这些氧化物电极上的丁醇氧化极化曲线,结果表明Ti/PbO2电极在加入SnO2,Sb2O3,PdOx中间层后,不仅电极的PbO2层不易脱落,而且使电极的电催化性能有较大的提高。 相似文献
93.
94.
催化裂化汽油脱硫添加剂USY/ZnO/Al2O3的性能评价 总被引:15,自引:0,他引:15
在固定流化床催化裂化装置上,以减压蜡油为原料,对制备的U\r\nSY/ZnO/Al2O3催化裂化汽油脱硫添加剂的性能进行了评价.结果表明\r\n,随着添加剂添加量和剂油比的增加,生成汽油的硫含量降低.在500\r\n℃和剂油比为5的条件下,在FCC平衡催化剂中添加30%的添加剂时,汽\r\n油的硫含量可由不加添加剂时的1230μg/g降低到770μg/g左右.添\r\n加剂的添加量(10%)较低时,对催化裂化产物的分布基本没有影响;\r\n添加30%的添加剂时,焦炭的产率有所增加,但汽油收率基本不变.X\r\nRD表征结果表明,USY/ZnO/Al2O3添加剂中的ZnO对USY的晶相结构有\r\n一定的破坏作用,但随着反应与再生次数的增多,ZnO与Al2O3之间形成\r\n较为稳定的锌铝尖晶石结构,使添加剂的性能趋于稳定. 相似文献
95.
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97.
Enn Lust Gunnar Nurk Silvar Kallip Indrek Kivi Priit Möller 《Journal of Solid State Electrochemistry》2005,9(10):674-683
The analysis of the medium temperature half-cell Ce0.8Gd0.2O1.9|70 wt% La0.6Sr0.4CoO3- (LSCO) + 30 wt % Ce0.8Gd0.2O1.9 (CGO) has been made by electrochemical impedance, cyclic voltammetry and chronoamperometry. The shape of complex impedance plots depends on temperature and cathodic polarisation of the electrode. Nyquist (Z, Z-) plots were fitted by equivalent circuit taking into account the electrolyte properties (at very high frequencies), charge transfer process at grain boundaries (at high frequencies), and medium and low frequency O2 reduction process at the cathode surface and inside the porous cathode material. Two different time constants have been obtained for the cathode process, i.e. for electroreduction of oxygen. It was found that the addition of CGO into the cathode material (LSCO) only somewhat decreases the surface catalytic activity but the noticeably higher low-frequency resistance (i.e. mainly diffusion-like mass transfer resistance RD) values at lower temperatures have been calculated. It was found that the mainly bulk diffusion-limited process at T773 K deviates toward the kinetically mixed process (diffusion + charge transfer) with increasing temperature. 相似文献
98.
A titanium dioxide sol with narrow particle size distribution was synthesized using TiCl4 as the starting material. The sol was prepared by a process where HCl was added to a gel of hydrated titanium oxide to dissolve it. The resulting aqueous titanic acid solution was heated to form titanium dioxide sol. The effects of preparation parameters were investigated. TiCl4 was slowly added to distilled water at 5°C. Aqueous solution of sodium hydroxide was added to adjust the pH of the system to 8–12. After aging for a period of time, the peptized sol was filtered and sufficiently washed. The filtered cake was repulped in water. Hydrochloric acid was slowly added to the solution with stirring. After condensation reaction and crystallization, a transparent sol with suspended TiO2 was formed. XRD results show that the crystalline phase was anatase. The suspended TiO2 particles were rhombus primary particles with the major axis ca. 20 nm and the minor axis ca. 5 nm. The TiO2 particles prepared at pH 8 had the largest surface area of 141 cm3/g and it was microporous. The compositions of the solution which yielded the smallest suspended TiO2 particles were TiO2:HCl (35% HCl) = 1:1 (molar ratio), concentration of TiO2 = 10%. Hydroxypropyl cellulose with viscosity of 150–400 cps was added as a dispersant. The sol was excellent in dispersibility and long-term stability. Transparent thin films could be obtained through dip-coating glass substrate in the sol. The dip-coating on glass can be less than three times to have one monolayer TiO2. The transparent TiO2 thin film had strong hydrophilicity after being illuminated by UV light. 相似文献
99.
Itsuo Furuoya 《Catalysis Surveys from Japan》1999,3(1):71-73
The vapor phase catalytic reaction between aromatic carboxylic acid and acetic acid was investigated. Many metal oxides catalyzed the reaction between 2methylbenzoic acid (OTA) and acetic acid (AA) to produce 2methylacetophenone (OMA), and weakly acidic oxides such as Th, U, Ce, and La oxide exhibited higher yield of OMA. The OMA yield depended on the catalyst support. SiO2, Al2O3, TiO2, and ZrO2 with a surface area of less than 200 m2 g–1 appeared to be suitable as industrial catalyst supports. CeO2 on Al2O3was chosen as an industrial catalyst for the synthesis of OMA because of higher productivity, longer catalyst life, and lifting of legal restrictions on catalyst handling. This catalyst system can also be applied to the syntheses of acetophenone, nitroacetophenone, and chloroacetophenone. 相似文献
100.
S.?FrangerEmail author P.?Berthet J.?Berthon 《Journal of Solid State Electrochemistry》2004,8(4):218-223
Ultrafine magnetite particles are prepared through an electrochemical process, at room temperature, from an iron-based electrode immersed in an alkaline aqueous medium containing complexing compounds. XRD and chemical analysis indicate that the product is pure magnetite, Fe3O4. The size and morphology of the particles are studied by SEM. The magnetite nanoparticles present a magnetoresistance of almost 3%, at 300 K, under a magnetic field of 1 T. A reactive mechanism for the electrochemical process is proposed. 相似文献