Authors:Y. Li, G. Fei, H. Xingen, L. Ruisen, and L. Zhen
Enthalpies of dilution at 298.15 K of aqueous solutions of THF and 1,4-dioxane have been determined using flow microcalorimetry.
The results obtained were used to determine the homotactic enthalpic interaction coefficients that characterize pair interactions
of THF and 1,4-dioxane in aqueous solution. These are briefly discussed from the point of view of intermolecular interaction
between the hydrated solute species.
Authors:Y. Li, G. Fei, Z. Honglin, L. Zhen, Z. Liqiang, and L. Ganzuo
The power–time curves of micellar formation of two anionic surfactants, sodium laurate (SLA) and sodium dodecyl sulfate (SDS),
in N,N-dimethyl acetamide (DMA) in the presence of various long-chain alcohols (1-heptanol, 1-octanol, 1-nonanol and 1-decanol)
were measured by titration microcalorimetry at 298 K. The critical micelle concentrations (CMCs) of SLA and SDS under various
conditions at 298 K were obtained based on the power–time curves. Thermodynamic parameters (
) for micellar systems at 298 K were evaluated according to the power–time curves and the mass action model. The influences
of the number of carbon-atom and the concentration of alcohol were investigated. Moreover, combined the thermodynamic parameters
at 303, 308 and 313 K in our previous work and those of 298 K in the present work for SLA and SDS in DMA in the presence of
long-chain alcohols, an enthalpy–entropy compensation effect was observed. The values of the enthalpy of micellization calculated
by direct and indirect methods were made a comparison.
Authors:L. Ji-zhen, F. Xue-zhong, H. Rong-zu, Z. Xiao-dong, Z. Feng-qi, and G. Hong-Xu
The thermal behavior of copper(II) 4-nitroimidazolate (CuNI) under static and dynamic states are studied by means of high-pressure
DSC (PDSC) and TG with the different heating rates and the combination technique of in situ thermolysis cell with rapid-scan
Fourier transform infrared spectroscopy (thermolysis/RSFTIR).
The results show that the apparent activation energy and pre-exponential factor of the major exothermic decomposition reaction
of CuNI obtained by Kissinger’s method are 233.2 kJ mol−1 and 1017.95 s−1, respectively. The critical temperature of the thermal explosion and the adiabatic time-to-explosion of CuNI are 601.97 K
and 4.4∼4.6 s, respectively. The decomposition of CuNI begins with the split of the C-NO2 and C-H bonds, and the decomposition process of CuNI under dynamic states occurs less readily than those under static states
because the dynamic nitrogen removes the strong oxidative decomposition product (NO2). The above-mentioned information on thermal behavior is quite useful for analyzing and evaluating the stability and thermal
charge rule of CuNI.