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171.
l引言管内或窄小流路内的自然对流沸腾CHF的研究比较少。文献[1~41对水及氟里昂系等液体进行了实验,在Kutataladze【’]的池内沸腾无量式基础上,提出如下经验公式当L/De--+0时上式退化为池内沸腾公式。式中qm。x是临界热通量;Hi。是蒸发潜热;。是汽液界面张力;尸l和p。分别是液体和蒸汽的密度;9是重力加速度;c是实验常数;不同研究者之间相差很大。当L/De较大时各经验公式的计算值会相差l~2倍。式(1)没有任何物理机理的支持,仅以J和L/De之间的无量纲关系对实验值进行统计整理,对物性的实际影响、De独立于L/De的… 相似文献
172.
Hien P. Z. Mai T. K. Quang T. X. Thuy T. N. 《Journal of Radioanalytical and Nuclear Chemistry》1986,105(6):351-355
The ko, Au-factors of 10 elements have been determined by irradating the samples with thermal neutrons in the reactor thermal column. The proposed method has the advantage of eliminating the errors induced by the uncertainties of the neutron spectrum parameters and the nuclear data. The results obtained are in good agreement with the literature data. 相似文献
173.
给出了弹性系统瞬时势能泛函的一般表达式,得到了其关于任意挠曲输液管道的具体表达式,根据瞬时最小势能原理建立了该结构的有限元动力方程,并首次推导出其离心力载荷公式,讨论了管道结构静平衡位置的发散流速的确定,最后,用简单的实验结果对理论分析作了验证。 相似文献
174.
A numerical method based on radial basis function networks (RBFNs) for solving steady incompressible viscous flow problems (including Boussinesq materials) is presented in this paper. The method uses a ‘universal approximator’ based on neural network methodology to represent the solutions. The method is easy to implement and does not require any kind of ‘finite element‐type’ discretization of the domain and its boundary. Instead, two sets of random points distributed throughout the domain and on the boundary are required. The first set defines the centres of the RBFNs and the second defines the collocation points. The two sets of points can be different; however, experience shows that if the two sets are the same better results are obtained. In this work the two sets are identical and hence commonly referred to as the set of centres. Planar Poiseuille, driven cavity and natural convection flows are simulated to verify the method. The numerical solutions obtained using only relatively low densities of centres are in good agreement with analytical and benchmark solutions available in the literature. With uniformly distributed centres, the method achieves Reynolds number Re = 100 000 for the Poiseuille flow (assuming that laminar flow can be maintained) using the density of , Re = 400 for the driven cavity flow with a density of and Rayleigh number Ra = 1 000 000 for the natural convection flow with a density of . Copyright © 2001 John Wiley & Sons, Ltd. 相似文献
175.
176.
Reversing the Stereoselectivity of a Palladium‐Catalyzed O‐Glycosylation through an Inner‐Sphere or Outer‐Sphere Pathway
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Shaohua Xiang Kim Le Mai Hoang Jingxi He Yu Jia Tan Prof. Dr. Xue‐Wei Liu 《Angewandte Chemie (International ed. in English)》2015,54(2):604-607
An efficient and concise method for the construction of various O‐glycosidic bonds by a palladium‐catalyzed reaction with a 3‐O‐picoloyl glucal has been developed. The stereochemistry of the anomeric center derives from either an inner‐sphere or outer‐sphere pathway. Harder nucleophiles, such as aliphatic alcohols and sodium phenoxides give β‐products, and α products result from using softer nucleophiles, such as phenol. 相似文献
177.
C‐Selective and Diastereoselective Alkyl Addition to β,γ‐Alkynyl‐α‐imino Esters with Zinc(II)ate Complexes
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Dr. Manabu Hatano Kenji Yamashita Mai Mizuno Orie Ito Prof. Dr. Kazuaki Ishihara 《Angewandte Chemie (International ed. in English)》2015,54(9):2707-2711
Since umpolung α‐imino esters contain three electrophilic centers, regioselective alkyl addition with traditional organometallic reagents has been a serious problem in the practical synthesis of versatile chiral α‐amino acid derivatives. An unusual C‐alkyl addition to α‐imino esters using a Grignard reagent (RMgX)‐derived zinc(II)ate was developed. Zinc(II)ate complexes consist of a Lewis acidic [MgX]+ moiety, a nucleophilic [R3Zn]? moiety, and 2 [MgX2]. Therefore, the ionically separated [R3Zn]? selectively attacks the imino carbon atom ,which is most strongly activated by chelation of [MgX]+. In particular, chiral β,γ‐alkynyl‐α‐imino esters can strongly promote highly regio‐ and diastereoselective C‐alkylation because of structural considerations, and the corresponding optically active α‐quaternary amino acid derivatives are obtained within 5 minutes in high to excellent yields. 相似文献
178.
A Highly cis‐Selective and Enantioselective Metal‐Free Hydrogenation of 2,3‐Disubstituted Quinoxalines
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Zhenhua Zhang Prof. Dr. Haifeng Du 《Angewandte Chemie (International ed. in English)》2015,54(2):623-626
A wide range of 2,3‐disubstituted quinoxalines have been successfully hydrogenated with H2 using borane catalysts to produce the desired tetrahydroquinoxalines in 80–99 % yields with excellent cis selectivity. Significantly, the asymmetric reaction employing chiral borane catalysts generated by the in situ hydroboration of chiral dienes with HB(C6F5)2 under mild reaction conditions has also been achieved with up to 96 % ee, and represents the first catalytic asymmetric system to furnish optically active cis‐2,3‐disubstituted 1,2,3,4‐tetrahydroquinoxalines. 相似文献
179.
The first montmorillonite‐supported surface single‐structure titanium complex: synthesis,characterization and catalytic activity in alkene epoxidation
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Wei Xu Bo Yu Huaming Sun Jindou Yang Ying Zhang Zhenhua Wang Xi Chen Guofang Zhang Ziwei Gao 《Surface and interface analysis : SIA》2015,47(3):308-314
A well‐defined single‐site titanium‐modified montmorillonite (MMT) with only one geometric construction ((?SiO)3–Ti–NMe2) was obtained in moderate conditions. Reaction of tetrakis(dimethylamido)titanium with hydroxylated MMT was conducted by surface organometallic chemistry technique, and the surface structure was characterized by in situ Fourier transform infrared spectroscopy, 13C cross polarization magic angle spinning nuclear magnetic resonance, X‐ray photoelectron spectroscopy, extended X‐ray absorption fine structure, and elemental analysis. The catalytic activity in alkene epoxidation was evaluated, and the results revealed that the steric hindrance of the substances is responsible for the catalytic activity of the MMT‐supported titanium complex but to the characteristic restricted layer‐like structure of the MMT. Copyright © 2014 John Wiley & Sons, Ltd. 相似文献
180.