波形钢腹板箱梁的约束扭转剪应力分析

基于周边不变形理论,结合闭口薄壁杆件约束扭转的计算分析,研究了波形钢腹板箱梁在约束扭转时混凝土悬臂板上扭转剪应力的分布,并进行了计算.通过对悬臂板在约束扭转中剪力流计算公式的推导,进一步阐述了其自由扭转剪应力及翘曲扭转剪应力的分布,指出了相关文献在这部分计算中存在的问题.通过一个简支波形钢腹板组合箱梁算例,将该文方法计算结果与ANSYS有限元计算结果进行比较.结果表明:在波形钢腹板箱梁截面中,主要由波形钢腹板承受扭转剪应力,其次是混凝土底板,底板剪应力最大值发生在底板中心处,其数值近似等于腹板剪应力的一半,而混凝土顶板和悬臂部分的扭转剪应力很小;该文计算的扭转剪应力结果在总体上符合有限元得到的扭转剪应力分布规律,在悬臂自由端为0,随着离开悬臂自由端距离的增大,扭转剪应力逐渐增大并达到峰值.     

Classification of Teleparallel Homothetic Vector Fields in Cylindrically Symmetric Static Space-Times in Teleparallel Theory of Gravitation

In this paper we classify cylindrically symmetric static space-times according to their teleparallel homothetic vector fields using direct integration technique. It turns out that the dimensions of the teleparallel homothetic vector fields are 4, 5, 7 or 11, which are the same in numbers as in general relativity. In case of 4, 5 or 7 proper teleparallel homothetic vector fields exist for the special choice to the space-times. In the case of 11 teleparallel homothetic vector fields the space-time becomes Minkowski with all the zero torsion components. Teleparallel homothetic vector fields in this case are exactly the same as in general relativity. It is important to note that this classification also covers the plane symmetric static space-times.     

Group-theoretical investigation of the tunneling splitting patterns of enolic acetylacetone

Extensive experimental and theoretical studies for enolic acetylacetone have been presented in the literature, but studies of the tunneling splitting patterns are still lacking. In this work we adopt the C_s symmetry equilibrium structure and apply a group-theoretical formalism to study the tunneling splitting pattern of the ground vibrational level of enolic acetylacetone. Enolic acetylacetone has three large-amplitude motions, one intramolecular hydrogen transfer and two methyl torsions. Therefore, the C_s structure of enolic acetylacetone has 18 (3 × 3 × 2) equivalent equilibrium molecular frameworks, nine (3 × 3) of them are from the two methyl torsions, and two are from the intramolecular hydrogen transfer. Tunneling motions among the 18 equivalent molecular frameworks split the ground vibrational level into eight sublevels: A₁, A₄, E₁, E₂, E₃, E₄, G(1) and G(2). In enolic acetylacetone the intramolecular hydrogen transfer induces a rearrangement of the CC, CO single and double bonds, and then triggers two additional 60° internal rotations, one in each of the two methyl groups attached to the hydrogen-bonded malonaldehyde ring. This interaction further complicates the tunneling splitting patterns and increases the difficulty of spectral analysis. In this work the influence of the intramolecular hydrogen transfer on the energy order of the eight sublevels is determined by a group-theoretical formalism.     

Twisted analytic torsion

We review the Reidemeister, Ray-Singer’s analytic torsion and the Cheeger-Mller theorem. We describe the analytic torsion of the de Rham complex twisted by a flux form introduced by the current authors and recall its properties. We define a new twisted analytic torsion for the complex of invariant differential forms on the total space of a principal circle bundle twisted by an invariant flux form. We show that when the dimension is even, such a torsion is invariant under certain deformation of the metric and the flux form. Under T-duality which exchanges the topology of the bundle and the flux form and the radius of the circular fiber with its inverse, the twisted torsion of invariant forms are inverse to each other for any dimension.     

余模范畴中的余倾斜预包络和余倾斜挠类

众所周知, Assem-Smal定理在倾斜理论中有重要的作用.本文的目的是建立一个在余模范畴中的Assem-Smal定理的版本,并通过利用预包络理论来刻画余模范畴中的余倾斜挠类.     

On finitely generated module whose first nonzero fitting ideal is maximal

Let R be a Noetherian ring and M be a finitely generated R-module. Let I(M) be the first nonzero Fitting ideal of M. The main result of this paper asserts that when I(M) = Q is a regular maximal ideal of R, then M?R∕Q⊕P, for some projective R-module P of constant rank if and only if T(M)?QM. As a consequence, it is shown that if M is an Artinian R-module and I(M) = Q is a regular maximal ideal of R, then M?R∕Q.     

Quantum-chemical calculations of the structure,vibrational spectra,and torsional and inversion potentials of methylcarbamate

We present results of ab initio and DFT calculations of the structure, potential functions of the methyl group internal rotation and the amino group inversion, and vibrational frequencies and intensities in IR and Raman spectra of methylcarbamate. The calculations were carried out using different basis sets in the HF, MP2, and DFT/B3LYP approximations. The influence of both the basis set size and the allowance for electronic correlation on peculiarities of the structure of the amino group in methylcarbamate has been analyzed. It is shown that the B3LYP/6-311++G(2d, p) and B3LYP/cc-pVDZ calculations reproduce highly accurately experimental geometric parameters of methylcarbamate. Parameters of torsional and inversion potentials and characteristics of vibrational spectra calculated in different approximations show satisfactory agreement with experimental values. Translated from Zhurnal Prikladnoi Spektroskopii, Vol. 76, No. 3, pp. 349–357, May–June, 2009.     

中国优秀物理学家的杰出代表——葛庭燧

回顾介绍了葛庭燧院士的生平和他在科学研究、人才培养方面所作出的贡献,展示了他的高尚情操,分析了他取得卓著成就的原因.     

Force field parameters for rotation around chi torsion axis in nucleic acids

To raise the accuracy of the force field for nucleic acids, several parameters were elaborated, focusing on the rotation around chi torsion axis. The reliability of molecular dynamics (MD) simulation was significantly increased by improving the torsion parameters at C8--N9--C1'--X (X = H1', C2', O4') in A, G and those at C6--N1--C1'--X in C, T, and U. In this work, we constructed small models representing the chemical structure of A, G, C, T, and U, and estimated energy profile for chi-axis rotation by executing numerous quantum mechanical (QM) calculations. The parameters were derived by discrete Fourier transformation of the calculated QM data. A comparison in energy profile between molecular mechanical (MM) calculation and QM one shows that our presently derived parameters well reproduce the energy surface of QM calculation for all the above torsion terms. Furthermore, our parameters show a good performance in MD simulations of some nucleic acids. Hence, the present refinement of parameters will enable us to perform more accurate simulations for various types of nucleic acids.