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71.
S. M. A. Shibli V. S. Dilimon V. S. Saji 《Journal of Solid State Electrochemistry》2007,11(2):201-208
It has been recently proved that RuO2 can act as an effective surface activator of aluminum alloy sacrificial anodes. TiO2 has the property of stabilizing RuO2 coating and resisting biofouling on metal surfaces. Hence, a mixed oxide catalytic coating of TiO2 and RuO2 can enhance the galvanic performance of aluminum alloy sacrificial anodes and resists biofouling on the anode surface. In the present work RuO2–TiO2 mixed oxide was coated on aluminum alloy sacrificial anodes. The large and uniform porous nature of the coating was found to facilitate efficient ion diffusion. The coating was found to persist on the anode even after 3 months of galvanic exposure. The anode having an optimum combination of the mixed oxide had 70% TiO2 as the major component in the coating. The catalytic coating significantly improved the performance of the anodes to a large extent. 相似文献
72.
Thomas C. Amu 《Journal of solution chemistry》1981,10(1):69-78
Interdiffusion coefficient have been measured for 1,1,2,2-tetrabromoethane in 21 organic solvents in order to ascertain the influence of shape, size, viscosity, nature and degree of branching, of the solvent molecules on transport properties. None of the existing correlations for diffusion in binary liquid systems appear to fit all the experimental data. Steric effects due to the solvent molecules are shown to be very important in the interpretation of the diffusion process. 相似文献
73.
粘土矿物的结构特征及其应用研究 总被引:2,自引:0,他引:2
阐述了贮量巨大、用途广泛的粘土矿物,其充分开发应用的关键,在于根据其结构特征,并通过适当的物理、化学方法加以改造、以适应各种不同工业应用的要求。并以我们对粘土矿物进行活化、改性、层间插入及其工业应用产品开发的初步研究成果,阐明利用粘土硅酸盐多层次结构的可变性,开拓新的应用性能的可能性及粘土矿物充分开发应用的途径。 相似文献
74.
A new technique, called modulated thermogravimetry, is introduced as a tool for obtaining continuous kinetic information for
decomposition and volatilization reactions. The approach makes use of an oscillatory temperature program to obtain kinetic
parameters during a mass loss. MTGA™ may be used under quasi-isothermal conditions to observe a single mass loss or may be
combined with linear heating rate or Hi-Res™ controlled rate thermogravimetry to scan from one mass loss region to another.
Results obtained are in agreement with those obtained by other kinetic methods.
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
75.
This is the second part of a paper which deals with the advantages and disadvantages of relative instrumental neutron activation
analysis concerning traceability and uncertainty, and the current scope and possible future extensions of neutron activation
analysis as a primary ratio method. The first part of this paper has been published in this Journal [1].
Received: 19 March 2001 Accepted: 2 October 2001 相似文献
76.
Recently the hydrogen-bond activated reactions have attracted much attention.1 Takemoto2 reported a highly enantioselective Michael addition of manolate to nitroolefins catalyzed by a bifunctional organocatalyst with tertiary amine and thiourea moiety. As we known,stereoselective conjugate additions of thiols are interesting due to the standpoint of biological and synthetic importance, however, only very limited good results have been obtained except for the works of Shibasaki3, Kanemasa4 and Deng5 et al.In this letter, we report an efficient catalytic asymmetric Michael reactions of thiols to a,a-unsaturated carbonyl compounds promoted by bifunctional organocatalysts. A series of organocatalysts with chiral amine and thiourea structures were designed and synthesized and have been successfully applied in the conjugated additions of thiols to a,a-unsaturated imides and enones.The reactions got quantitative yields and the ee values were up to 84%. It is noteworthy that the a-asymmetric protonation (up to 43% ee) also could be achieved.The Michael addition between aromatic thiols and a,a-unsaturated carbonyl compounds isdescribed as follows:Works to further increase the enantioselectivity is under investigation in our laboratory. 相似文献
77.
78.
Summary Kinetics of dehydration of equilibrium swollen poly(acrylic acid) hydrogel was investigated using methods of non-isothermal
thermal analysis. Methods of Kissinger, Coats-Redfern, Van Krevelen and Horowitz-Metzger were applied for determination the
kinetics parameters: activation energy (E), pre-exponent (lnA) as well as the kinetics model ƒ(69) for the process of hydrogel dehydration under different heating rates. An existence
of good agreement between determined values of kinetic parameters (Eand A), which were obtained applying different methods under the same heating rate. Functional relationship between changes of
kinetic parameters of dehydration and changes of heating rate was established. An existence of compensation effect is accepted
and explanation of compensation effect appearance during the hydrogel dehydration is suggested. 相似文献
79.
The degradation process of TEOS-PDMS Ormosils containing different amounts of γ -APS has been studied by means of DTA, TG, FTIR and 29Si-NMR measurements. It has been found that the amount of γ -APS improved the thermal properties of Ormosil materials. The increase in γ -APS content causes the increment on the decomposition temperatures and activation energies of the studied Ormosils. These results have been attributed to the favourable effect of γ -APS in the copolymerisation reaction between TEOS and PDMS molecules. 29Si-NMR analyses have shown that the incorporation of γ -APS increases the concentration of D(Q) units in the Ormosil structure, i.e., increases the number of TEOS molecules bonded to PDMS ones. Initial decomposition temperature (IDT), temperature of maximum weight loss rate (Tmax), integral procedure decomposition temperature (IPDT) and activation energy values (E) were calculated from different equations which described the degradation of these materials. Addition of 10 wt% γ -APS produced an increase of 63∘C in the IDT and of 115 and 110∘C, respectively, for Tmax and IPDT (up to 478 and 610∘C) compared to the free γ -APS Ormosil. Activation energy values also rise up to 69.4 kJ⋅ mol−1 by introducing 10 wt% of γ -APS. 相似文献
80.