Bi系高温超导带材冷压工艺优化试验

采用套管法（ＰＥＴ）制备Ｂｉ系高温超导带材,进行了冷压工艺的优化研究。试验结果表明,Ｂｉ系带材所能承受的压力有一个限值,若超过这个限值后,密度虽可提高,但晶粒破碎严重Ｊｃ值反而降低,带材优化的冷压工艺参数是８３８℃／６０ｈ＋冷压＋８３８℃／６０ｈ。第１次压力为２ＧＰａ,第２次２．５ＧＰａ;冷压压下速率为１．５×１０＾－４ｍｍ／ｓ。同时研究还表明冷压的主要作用是提高带材的致密度和晶粒取向度,最终改善     

变质量高阶非线性非完整系统的相对论性Kane方程

本文在同时考虑经典变质量和相对论变质量的情况下,由相对论性成有Ｄ’Ａｌｅｍｂｅｒｔ原理推导出变质量高阶非线性非完整系统的相对论性Ｋａｎｅ方程。     

不同贮藏条件下鳗骨油氧化特性的研究

研究了室温下（15℃）鳗骨油在空气中的自氧化速度,以及温度和贮藏条件对鳗骨油氧化速度的影响。实验所设的温度梯度分别为6℃、15℃、35℃,贮藏条件分别是敞口,密封（蜡封）和用N2驱除氧气后密封保存。实验结果显示,室温下鳗骨油在空气中的自氧化速度,敞口存放4天,过氧化值就已超过0.15;温度和贮藏条件对鳗骨油的氧化速度有显著影响,驱除氧气低温贮藏可以有效地防止鳗骨油的氧化。     

茶叶矿质元素浸出量与茶叶冲泡时间及冲泡次数的关系

研究了茶汤中茶叶１０种矿质元素（Ｋ、Ｃａ、Ｍｇ、Ｐ、Ａｌ、Ｆｅ、Ｍｎ、Ｓｒ、Ｂａ、Ｚｎ）的浸出量与茶叶冲泡次数以及冲泡时间的关系．结果表明：（１）茶叶中１０种元素的浸出量与茶叶冲泡次数之间具有显著的指数函数相关,相关方程为ｙ＝ａｅ－ｂｘ,１０种元素的浸出量与茶叶冲泡时间之间具有显著的对数函数相关,相关方程为ｙ＝ａ＋ｂｌｇｘ,各元素在两方程中的相关显著性均为α＜０．０１;（２）性质相近的元素,如Ｂａ与Ｓｒ在上述函数中的变化行为更为相近;（３）元素Ｋ、Ｚｎ、Ａｌ、Ｍｇ浸出比在３０％以上,可认为是易浸出元素,而元素Ｍｎ、Ｆｅ、Ｓｒ、Ｂａ、Ｃａ的浸出比低于３０％,可认为是较难浸出元素;（４）茶叶与茶汤之比为１∶１０,冲泡水温１００℃,冲泡时间２分钟,３泡茶汤已能充分利用茶叶中常见的人体营养元素Ｋ、Ｍｇ、Ｐ、Ｍｎ、Ｚｎ,元素浸出量与总浸出量之比在６０％以上．     

3,5-diBr-PADAP作锆(Ⅳ)显色剂的分光光度法研究与应用

本文研究了在非离子表面活性剂存在下,用3,5-diBr-PADAP作锆显色剂的胶束增溶分光光度法。在pH1.0～2.0的HCl介质中,配合物吸光度最大且稳定,最大吸收值在610nm处。Zr(Ⅳ)与试剂形成1:2的配合物,摩尔吸光系数为1.10×10~5L·mol~(-1)·cm~(-1),zr(Ⅳ)量在0～30μg/25mL范围内遵守比尔定律。采用钽试剂一苯苹取分离法,适合于钽铌矿中微量锆的测定。     

Tuning of the alpha-terthiophene radical cation coupling reaction using mixed micelles with varying charge density.

The photophysics and photochemistry of alpha-terthiophene (alphaT), compartmentalized in mixed nonionic/anionic micelles, have been investigated with focus on the influence of the micellar surface charge density on the formation of the radical coupling product alpha-hexathiophene (alphaH). By varying the ratio of nonionic-to-anionic surfactants, and assuming ideal mixing, the charge density of the mixed micelles was varied. From Poisson-Boltzmann calculations, performed using the cell model, the electrostatic potential and the counterion activity were estimated as a function of the distance from the micellar surface. Upon excitation, the triplet state of alphaT is formed, from which the alphaT radical cation can be formed by absorption of a second photon. The radical cation can form alphaH if it encounters another alphaT radical cation. Under the experimental conditions used, this implies that the alphaH formation only occurs if the compartmentalized radical cation is able to migrate from its host micelle to another micelle, either via the surrounding bulk or by fusion of two micelles followed by mixing of their contents before micellar fission. The formation yield of the radical cation depends on the charge density of the mixed micelle; a lower charge density, that is, an increased amount of nonionic surfactant, lowers the yield. The yield of the coupling product alphaH, however, does not follow the same trend. A maximum yield of alphaH is found at intermediate nonionic surfactant molar ratios. This behavior is understood in terms of the Poisson-Boltzmann simulation results and by comparing charge-density changes as a function of molar fraction with the changes in counterion activity. The alphaH yield is a result of the balance between an increased possibility of radical cation bulk migration and a lowered electrostatic stabilization of the radical.     

A density functional theory study on the electrocyclization of 1,2,4,6-heptatetraene analogues: converting a pericyclic to a pseudopericyclic reaction

A comprehensive B3LYP/6-31+G* study on the electrocyclization of 1,2,4,6-heptatetraene analogues was conducted. Starting from the cyclization of (2Z)-2,4,5-hexatrienal, a pericyclic disrotatory process favored by the assistance of a electron lone pair, we incorporated small modifications in its molecular structure to obtain a truly pseudopericyclic process. To this purpose electronegative atoms (fluorine and nitrogen) were added to give a more electrophilic character on the carbon atom which is attacked by the electron lone pair of the oxygen atom. The complete pathway for each reaction was determined, and changes in magnetic properties were monitored with a view to estimating the aromatization associated with each process. This information, together with the energetic and structural results, allowed us to classify the reactions as pseudopericyclic or pericyclic. Among all studied reactions only one was a truly pseudopericyclic process and another was a borderline case. The features of this unequivocally pseudopericyclic case were analyzed in depth.     

Solubility of Triethylamine in Tetraethylammonium Chloride Aqueous Solutions from 20 to 35°C

Solubilities of triethylamine in aqueous tetraethylammonium chloride solutions were measured at 20, 25, and 35°C. The molalities in Et₄NCl of the aqueous solvents ranged from 0.03 to 1 mol-kg^–1. The data were evaluated from density measurements using a vibrating-tube densimeter. At each temperature, least-squares method was used to fit experimental density data points to double polynomial equations of various degrees. Triethylamine molalities of the saturated aqueous phases were estimated by extrapolation from those equations. Experimental data were interpreted in terms of hydrophobic and electrostatic perturbed domains in the hydration shells of the noneleceory and of the cation of the salt, as a function of temperature and salt concentration. The conclusions obtained are consistent with previous volumetric studies.     

Influence of Cycle Temperatures on the Thermochemical Heat Storage Densities in the Systems Water/Microporous and Water/Mesoporous Adsorbents

The adsorption equilibrium of water on microporous adsorbents (zeolites of NaA-, NaY- and NaX-type as well as their ion exchanged forms) and on mesoporous adsorbents (different silica gels and composite material i.e. silica gel + salt hydrate) has been studied experimentally and theoretically. Using the Dubinin theory of pore filling the characteristic curves of the adsorption systems and other relevant dependences such as isotherms, isobars, isosteres and the curve of the differential heat of adsorption were calculated. For all systems investigated the adsorption were calculated. A_ads and the desorption potential A_des of the closed heat storage system were estimated. These values define the working range of the adsorption/desorption cycle and allow to calculate the specific heat storage density Δ h_sp. On the basis of Δ h_sp the different adsorbents were compared in order to select the optimal porous storage material for a given application. The presented experimental and theoretical investigations show that the adsorption systems water-zeolite and water-composites are promising working pairs for thermochemical heat storage processes for hot tap water supply and space heating of single family dwellings. The advantage of the water-composite system is the low desorption temperature (solar energy) the main shortcoming the low temperature lift. The advantage of the water zeolite system is the high temperature lift, the shortcoming are the relative high desorption temperatures.     

Effect of Neck Formation on the Measurement of Dynamic Interfacial Tension in a Drop Volume Tensiometer

Dynamic interfacial tension values obtained by drop volume tensiometry will be affected under certain experimental conditions by the formation of a neck between the drop and the capillary tip. This phenomenon must be accounted for to obtain accurate values of interfacial tension. In this work, neck formation for a water–mineral oil system is studied under conditions where hydrodynamic effects can be neglected. A model originally developed for the determination of the surface tension of a suspended drop is modified for application to dynamic interfacial tensions of surfactant-containing liquids. The model relates apparent values of interfacial tension calculated from drops possessing necks to actual values. Experiments with Span 80 (sorbitan monooleate) and sodium dodecyl sulfate (SDS) surfactants in a mineral oil–water system are used to test the validity of the developed model. For the small tip diameter used, good agreement is obtained for Span 80 up to the critical micelle concentration, and for low concentrations of SDS, when the surfactant adsorption is diffusion-limited. In both cases, the neck diameter of the growing drop can be considered constant over the range of dynamic interfacial tensions tested.