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81.
An exfoliated poly(4,4-oxybis(benzene)disulfide) (POBDS)/vermiculite (VMT) nanocomposite was prepared by using cyclo(4,4-oxybis(benzene)disulfide) (COBDS) oligomers and cetyltrimethyl ammonium bromide exchanged VMT. The POBDS/VMT nanocomposites were fabricated in two steps. First, the COBDS oligomers were used to swell and exfoliate organo VMT to afford COBDS-VMT nanocomposite precursor. Subsequently, the exfoliated POBDS-VMT nanocomposite can be made via in situ and instant melt ring-opening polymerization of the COBDS-VMT nanocomposite precursor. High molecular weight POBDS polymer can be formed in a few minutes. The nano scale dispersion of VMT layers within POBDS polymer was confirmed by both the X-ray diffraction patterns and TEM examinations. This methodology provides a potential approach to synthesize high performance polymer nanocomposite.  相似文献   
82.
用溶胶-凝胶法制备了在可见光照射下具有光催化活性的掺杂P(t Ⅳ)离子的非晶态微孔TiO2,表面积为160~200 m2/g;含3.0%Pt(Ⅳ)的AMM-Ti具有最大的光催化活性. X射线精细结构分析(EXAFS)表明,单个的PtCl4分子均匀地分布在非晶态二氧化钛表面;用这种光催化剂降解2,4-二氯苯氧基乙酸时,2,4-二氯苯酚是主要的中间物,通过Langmuir-Hinshelwood 方程的线性形式估算了反应速率常数k 和吸附平衡常数K,研究了光催化起始反应速率和反应物起始浓度之间的关系,同时,提  相似文献   
83.
We have carried out a systematic structural, electric, and magnetic study on Y---Pd---B---C samples with different compositions with emphasis on the as-cast and annealed YPd5B3C0.3 which was first reported to superconduct at 23 K by Cava et al. We found that the tetragonal body-centered YPd2B2C with lattice parameters a=3.71 Å and c=10.81 Å is the phase responsible for the 23 K superconductivity and that YPd2B2C is metastable, which is consistent with the suggestion made by Cava et al. [1]: it is not stable at high temperatures nor stabilizable by Ni doping, although its isostructural compound, YNi2B2C, exists. Two new phases with Y:Pd ratios of 1:7 and 2:3, respectively, have also bee detected.  相似文献   
84.
本文通过对脉管内自然对流的数值模拟,讨论了当脉管冷端处在不同方向时,脉管内的自然对流对脉管制冷机性能的影响.数值模拟结果表明,当冷端在下时获得的制冷温度最低;当热端在下并与重力方向成30°时制冷温度最高.结论与实验测量结果定性一致.所做的理论分析对实现脉管制冷机的良好运行有指导意义。  相似文献   
85.
This paper introduces the principles, instrumentation, implementation, and industrial applications of an on-line thermal neutron prompt-gamma element analysis system (using a252Cf neutron source, Am–Be neutron source, or neutron generator). The energy resolution of the system at the H prompt-gamma full-energy photopeak (2.22325 MeV) is 3.6 keV. The concentration measurement error of Al2O3, FeO3, CaO, and SiO2 is ±0.3%, ±0.1%, ±0.4%, and ±0.4%, respectively. The system has been tested on-site at both the Shandong and the Zhengzhou Aluminium Works. Our preliminary on-site measurements confirm that the stability, reliability, measurement range, and accuracy of the system can meet the requirements of the aluminium production process. Facilitation of this measurement at aluminium plants is expected to reduce plant costs by over 3 million dollars annually through reduced energy consumption, more rapid qualification of pulps being mixed during the production process, and in reduced labor costs.Other participants of Shandong and Zhenghou Aluminium Works are: Wang Aili, Zengshen, Dei Jianguo and Lu Jinnan, Wang Deyu, Jin Hequan.  相似文献   
86.
Seven new highly oxygenated nortriterpenoids, rubriflorins D–J ( 1 – 7 ), were isolated from the leaves and stems of Schisandra rubriflora, and their structures were elucidated on the basis of extensive analysis of spectroscopic data. These new compounds feature the opening of ring A compared with related known nortriterpenoids isolated from the genus Schisandra and showed weak activity against HIV‐1.  相似文献   
87.
The thermal behavior of two new non-linear optical (NLO) materials, urea-(D) tartaric acid (UDT) and urea-(DL) tartaric acid (UDLT) were studied by using DSC, TG and TMA. The results show that: 1) The two crystals have different melting points but similar decomposition temperatures due to the influences of intermolecular forces, which is attributed to the stereo effects of (D)-tartaric and (DL)-tartaric acid molecules; 2) There was only thermal expansion and no thermal contraction when the UDT and UDLT crystals were heated; 3) There was no phase transition within the measured temperature range; 4) The thermal expansion of the UDT and UDLT crystals shows a small anisotropy; 5) The specific heats of UDT and UDLT change linearly with temperature in the measured temperature range and the value for UDT is 1.321 J g-1 K-1 at 320 K while the specific heat of UDLT is 1.357 J g-1 K-1 at the same temperature. This revised version was published online in July 2006 with corrections to the Cover Date.  相似文献   
88.
铽-甲基吲哚乙酰丙酮三元配合物发光过程研究   总被引:1,自引:0,他引:1  
测定和分析了RE.L1.L2(RE=Tb(Ⅲ)、Gd(Ⅲ),L1=3M(3甲基吲哚-1-乙酰基丙酮),L2=TPPO、Phen、Dipy)三元配合物的荧光光谱、磷光光谱、磷光寿命及变温荧光光谱等.讨论了Tb(Ⅲ)与配体之间的能级匹配和L1与L2的三重态之间传能的问题,说明了影响这些三元配合物荧光效率的主要因素及其发光过程.  相似文献   
89.
The terephthalate dianion and the bis(imidazolyl)benzene ligand of the title compound, {[Zn(C8H4O4)(C20H14N4)]·C2H6O}n, each bridges two adjacent zinc centers, resulting in a layer‐type coordination polymer; the zinc center shows tetrahedral coordination. The disordered ethanol solvent molecules occupy the spaces between the layers and are hydrogen bonded to the layers. The two symmetry‐independent dianions lie on different inversion sites.  相似文献   
90.
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