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排序方式: 共有177条查询结果,搜索用时 31 毫秒
1.
Xu Yongjian Yu Ling Liang Lizhen Hu Chundong Xie Yahong Xie Yuanlai Jiang Caichao Liu Sheng Wei Jianglong Liu Zhimin Sheng Peng Tao Ling 《Journal of Thermal Analysis and Calorimetry》2020,139(1):527-533
Journal of Thermal Analysis and Calorimetry - According to EAST’s experimental plan, the long-pulse and high-power operation of neutral beam injector is the requirement for EAST. In this... 相似文献
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Zhaoqi Ye Dr. Yang Zhao Dr. Hongbin Zhang Prof. Yahong Zhang Prof. Yi Tang 《Chemistry (Weinheim an der Bergstrasse, Germany)》2020,26(28):6147-6157
For zeolite catalysts, the regulation of active site and pore structure plays an important role in the enhancement of their catalytic performance. In this work, a one-pot and organic template-free co-regulation route is proposed to straightforwardly synthesize basic mesoporous ZSM-5 zeolites with adjustable alkaline-earth metal species. The synthesis pathway combines two decisive strategies: 1) the seed-induced interface assembly growth method and 2) the acidic co-hydrolysis/condensation of aluminosilicate species and alkaline-earth metal (e.g., Mg, Ca, Sr, or Ba) sources. It is interesting that the mesoporous structure was self-evolved through particle-attached seed-interfacial crystallization without the assistance of any template. Meanwhile, the incorporation of alkaline-earth metals species is homogeneous and highly dispersed in the solid products during the whole crystallization process, and finally generate the superior basicity. Catalysis tests of the as-synthesized samples displayed their novel performance in the typical base reaction of Knoevenagel condensation, even for bulky substrates owing to the enhanced diffusion arising from the meso/microporous network. This finding opens new possibilities for facile, cost-effective, and environmentally friendly synthesis of mesoporous high-silica zeolites with tunable acid/base properties, and deepens our understanding of the particle-attached crystallization. 相似文献
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The polyaniline water hydrogen-bonded complex was studied by first-principles calculation. The density functional theory method was used to calculate the structure characters, natural bond orbital charge distribution, infrared spectra and the frontier molecular orbital. Results showed that the H–O···H–N and C–N···H–O type intermolecular hydrogen bonds were formed. The bonds involved in the intermolecular H-bond were all influenced by the hydrogen bonding interaction. During the hydrogen bond formation, the polymer chains in the complexes were all charged, which can be an important factor contributing to the increase of electrical conductivity. The N1–H vibration was strongly influenced, and the locations as well as the intensities of N1–H absorption bands were all changed in the complexes. In the orbital transition of HOMO to LUMO, the electron density transferred from benzenoid ring to quinoid ring. 相似文献
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Yaru Qin Qian Gao Yanmei Chen Wei Liu Feng Lin XiangFei Zhang Yaping Dong Yahong Li 《Journal of Cluster Science》2017,28(3):891-903
The incorporation of LnIII ions into the 12-metallacrown-4 topology affords the formation of four mixed 3d-4f pentanuclear complexes of compositions [NH(C2H5)3]{[Ln(OAc)4] [12-MC Mn III (N)shi-4]}·xH2O (Ln = Sm (1), Gd (2), Tb (3), Dy (4); x = 0.5 for 1 and 3, x = 0.25 for 2, x = 0 for 4; H3shi = salicylhydroxamic acid). Compounds 1–4 were obtained from the reactions of H3shi with Mn(CH3COO)2·4H2O and Ln(NO3)3·6H2O, in the presence of N(C2H5)3. They all contain a crown-like [Mn4Ln(μ-NO)4]11+ core with four MnIII atoms being at the rim of the crown and an LnIII ion occupying the dome of the crown. The peripheral ligation about the core is provided by four η1:η1:µ acetate groups. The identity of the LnIII ions slightly affects the 12-metallacrown-4 frameworks, as demonstrated by the gradual decrease of the distances between the LnIII ions and the centres of the Mn4 planes (1.85 Å for 1, 1.81 Å for 2, 1.80 Å for 3, and 1.77 Å for 4). Variable-temperature dc magnetic susceptibility studies were carried out on polycrystalline samples of 1–4. Antiferromagnetic interactions are determined for complexes 1–4. 相似文献
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Crystal structure of meso‐substituted pyrazolyl porphyrin complexes and their highly active catalyst for oxidation of alkylbenzenes 下载免费PDF全文
During the past few years, a great deal of effort has been devoted to the anchoring of catalytic oxidation. In this work, three new catalysts CuPp, MnPp and ZnPp by solvothermal methods with 5, 10, 15, 20‐tetrakis(4‐N‐pyrazolyl)‐phenyl porphyrin (H2Pp) and the corresponding metal salts have been synthesized and structurally characterized. The single crystal structures determined by X‐ray diffraction show the bond distances of M‐N in porphyrin cores determined the conformation of porphyrin rings. We explored the catalytic activity of CoPp, CuPp, MnPp and ZnPp for oxidation of alkylbenzenes. The experimental results display these products exhibit high catalytic activities and selectivities for oxidation of ethylbenzene to acetophenone, and can be reused by filtration without appreciable decrease in catalytic activity and selectivity. 相似文献
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In this paper, we investigate the dynamics of the inverted pendulum with delayed feedback control. The existence and stability of multiple equilibria depending on the control strengths are studied. Taking the time delay of the control terms as a parameter, periodic oscillations induced by delay are found. By using the method of multiple scales, the effect of the control gains and the relative mass of the pendulum on the stability and direction of Hopf bifurcations are discussed. Numerical simulations are employed to illustrate the obtained theoretical results. 相似文献