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91.
顺—反异构体的研究,在配合物化学中占有重要的地位。二水二草酸合铬酸钾这一配合物顺、反异构体的制备和异构化现象的研究已有报导,但多限于水溶液体系。也有关于该配合物热稳定性和热分解动力学研究的报导但对固相中该配合物异构体转变的研究尚未见报导。本文利用DTA方法,对二水二草酸合铬酸钾顺、反异构体的制备以及固相中异 相似文献
92.
An evaluation of measurements of heat capacities by modulated differential scanning calorimetry, MDSC is presented. Heat capacities were obtained from 130 to 550 K by a non isothermal technique in which a periodic modulation was added to the linear heating rate. Effects of amplitude and period of modulation, sample weight, sample type, pan type, and cell imbalance are described. Results are compared with those obtained using the isothermal technique. Heat capacity could be measured well into the decomposition region and separated from the non reversing signal due to chemical reaction (degradation), thus allowing a precise detection of onsets of the thermal degradation. This additional information will aid in the interpretation of the degradation chemistry, a field vital for the petroleum-industry.Dedicated to Professor Bernhard Wunderlich on the occasion of his 65th birthdayPart of this paper was presented at the 23rd Conference of the North American Thermal Analysis Society, Toronto, Canada, September 25–28, 1994.The author (MVN) acknowledges the experimental assistance provided by J. Balogh of Exxon Research and Engineering Company, Linden. Helpful discussions with A. Boller of the University of Tennessee at Knoxville, Dr. Y. Jin, General Electrical, and Dr. S. Sauerbrunn formerly of TA Instruments are also acknowledged. 相似文献
93.
The surface free energies of polyethylene terepthalate fibers with different draw ratios were experimentally determined by contact angle measurements inn-alkane/water systems. The dispersive component of the surface free energy increased with increasing draw ratio, whereas the nondispersive one remained almost constant. After heat treatment, the dispersive surface free energy increased, but was reduced above 140°C. The nondispersive component increased by heat treatment at 190°C. The increases in the density and birefringence of the fibres due to the drawing and heat treatment suggested that the increase in the dispersive surface free energy was caused by the increase in the atomic density at the fiber surface due to drawing and heat treatment. ESCA results indicated that the increment in the nondispersive surface free energy due to heat treatment was caused by the addition of functional groups to the fiber surface due to heat treatment. 相似文献
94.
稀土高氯酸盐-谷氨酸配合物[Pr2(L-α-Glu)2(ClO4)(H2O)7](ClO4)3•4H2O的低温热容和热化学研究 总被引:1,自引:0,他引:1
合成了一种稀土高氯酸盐-谷氨酸配合物. 经TG/DTG、化学和元素分析、FTIR及与相关文献对比, 确定其组成为[Pr2(L-α-Glu)2(ClO4)(H2O)7](ClO4)3•4H2O, 纯度为99.0%以上. 利用显微熔点仪分析发现其没有熔点. 在78~370 K温区, 用精密绝热量热仪测量其低温热容, 在285~306 K温区发现一明显吸热峰, 归结为固-固相变过程. 通过相变温区三次重复热容测量, 得到相变温度Ttr、相变焓ΔtrHm和相变熵ΔtrSm分别为(297.158±0.280) K, (12.338±0.016) kJ•mol-1和(41.520±0.156) J•K-1•mol-1. 用最小二乘法将非相变温区的热容对温度进行拟合, 得到了热容随温度变化的两个多项式方程. 用此方程进行数值积分, 得到每隔5 K的舒平热容值和相对于273.15 K的热力学函数值. 根据TG/DTG结果, 推测了该配合物的热分解机理. 依据Hess定律, 选择1 mol•dm-3盐酸为量热溶剂, 利用等温环境溶解-反应量热计, 测定了该配合物的标准摩尔生成焓为: ΔfHm0=-(7223.1±2.4) kJ•mol-1. 相似文献
95.
微量热法研究γ-Mo2N催化剂表面氢的微分吸附热 总被引:1,自引:0,他引:1
Differential heats of H 2 adsorption on γ-Mo2N catalysts were studied by using microcalorimetry. Samples with high and medium surface areas (90 and 17 m2•g -1 ) present a homogeneous energetic distribution of surface sites, which corresponds with the preferential orientation of their (200) planes. Molybdenum nitride with low surface area (8 m2•g -1 ) displays a heterogeneous energetic distribution of H 2 adsorption sites. The higher initial differential heat of hydrogen adsorption observed for the low surface Mo nitride was attributed to species adsorbed on surface sites associated with the (111) plane. 相似文献
96.
Calorimetry has been used in the investigations of calcium aluminate materials produced as a binder for aluminate-corundum
composites of high refractoriness. The kinetics and of hydration process was thus characterized and the optimum compositions
of initial binders and cement-corundum refractory filler blends could be selected for further tests. The acceleration of heat
evolution - the shortening of so-called induction period and relatively high heat output in the presence of corundum was observed.
It means the acceleration of hydration process, that is early crystallisation of hydration products and subsequent further
dissolution of initial anhydrous aluminate phases. In the presence of fine grained corundum particles these phenomena should
be attributed to the nucleating effect of fine corundum particles.
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
97.
Penna Thereza Christina Vessoni Marques Marcelo Machoshvili Irena A. Ishii Marina 《Applied biochemistry and biotechnology》2002,98(1-9):539-551
Large-volume parenteral solutions were submitted to heat treatments after being inoculated with Bacillus stearothermophilus ATCC 7953 (T
r
=121°C) and Bacillus subtilis ATCC 9372 (T
r
=104.5°C) spores. The average decimal reduction time for B. stearothermophilus ranged from a D
121°C value of 1.31 to 3.14 min, in glucophysiologic and Ringer’s solutions respectively. For B. subtilis, D
104.5°C value increased from 0.69 to 1.37 min, in Ringer’s (pH=5.91) and 50% glucose (pH 3.05) solutions respectively. The z value ranged from 7.95°C (20% mannitol solution) to 13.14°C (50% glucose solution), corresponding to an activation energy
(Ea) of 81.48 and 49.30 kcal/mol, respectively. 相似文献
98.
热管冷却反应堆采用非能动传热技术,热响应速度快,可避免堆芯单点失效,具有功率密度大、寿命长、环境适应性强、工作性能稳定等特点,是目前空间核反应堆研究的热点。本文基于清华大学开发的反应堆蒙特卡洛中子输运程序RMC (Reactor Monte Carlo code),以美国爱荷华国家实验室(Idaho National Laboratory, INL)设计的热管冷却反应堆INL Design A为研究对象,选取3种热管工质开展热管冷却反应堆堆芯物理计算。计算结果表明:锂热管工质不仅拥有很好的热物性参数,并且使用锂热管工质的热管冷却反应堆缓发中子有效份额最大、中子能谱较硬、燃耗反应性损失最小、增殖性能最佳,有利于热管冷却反应堆堆芯小型化与长寿命。因此,推荐锂为热管冷却反应堆的热管工质。 相似文献
99.
100.
A. Zielenkiewicz K. Busserolles G. Roux-Desgranges A. H. Roux J-P. E. Grolier W. Zielenkiewicz 《Journal of solution chemistry》1995,24(7):623-632
Densities and specific heat capacities of ternary aqueous systems containing dipeptides (glycyl-glycine or L--alanyl-L--alanine) and nucleic acid bases (cytosine or thymine) or their alkyl derivatives (1,3-diethylthymine or caffeine) were determined at 25°C by flow calorimetry and flow densimetry. The partial molar volumes and heat capacities of transfer at infinite dilution of the different nucleic acid bases from water to water+dipeptide solutions were obtained therefrom. Except for the case of the transfer of cytosine to aqueous glycyl-glycine solutions where a small positive dependence of the transfer quantities was observed with the dipeptide concentration, the values of the heat capacities of transfer were in general low, positive or negative, depending on the compensation of hydrophobic-hydrophilic interactions between the dipeptide and the base. The volumes of transfer of most of the bases are very small, within the limit of the experimental error. 相似文献