Energy Conservation with Non-Symplectic Methods: Examples and Counter-Examples

Energy conservation of numerical integrators is well understood for symplectic one-step methods. This article provides new insight into energy conservation with non-symplectic methods. Sufficient conditions and counter-examples are presented. AMS subject classification (2000) 65L06, 65P10, 37J99.Submitted June 2004. Accepted October 2004. Communicated by Syvert Nørsett.     

Excavations in molecular crystals

Single crystals built from porous molecular networks can react with agents that penetrate the crystals, cleave fragments from the network, and thereby increase the volume available for guests, all without loss of crystallinity.     

An Algebraic Approach to Invariant Preserving Integators: The Case of Quadratic and Hamiltonian Invariants

In this article, conditions for the preservation of quadratic and Hamiltonian invariants by numerical methods which can be written as B-series are derived in a purely algebraical way. The existence of a modified invariant is also investigated and turns out to be equivalent, up to a conjugation, to the preservation of the exact invariant. A striking corollary is that a symplectic method is formally conjugate to a method that preserves the Hamitonian exactly. Another surprising consequence is that the underlying one-step method of a symmetric multistep scheme is formally conjugate to a symplectic P-series when applied to Newton’s equations of motion.     

Microwave-assisted synthesis of α-ethoxycarbamates

An efficient and reproducible synthesis of various α-ethoxycarbamates is described via a microwave heating mode. Compared to the thermal process, the microwave dielectric heating induces a dramatic reduction of the reaction time and the improvement of the yields. The reaction is general since applicable to aromatic and aliphatic aldehydes with various primary amines. Several examples involving chiral aldehydes have also been considered.     

Aqueous suspensions of natural swelling clay minerals. 2. Rheological characterization

We report in this article a comprehensive investigation of the viscoelastic behavior of different natural colloidal clay minerals in aqueous solution. Rheological experiments were carried out under both dynamic and steady-state conditions, allowing us to derive the elasticity and yield stress. Both parameters can be renormalized for all sizes, ionic strength, and type of clay using in a first approach only the volume of the particles. However, applying such a treatment to various clays of similar shapes and sizes yields differences that can be linked to the repulsion strength and charge location in the swelling clays. The stronger the repulsive interactions, the better the orientation of clay particles in flows. In addition, a master linear relationship between the elasticity and yield stress whose value corresponds to a critical deformation of 0.1 was evidenced. Such a relationship may be general for any colloidal suspension of anisometric particles as revealed by the analysis of various experimental data obtained on either disk-shaped or lath- and rod-shaped particles. The particle size dependence of the sol-gel transition was also investigated in detail. To understand why suspensions of larger particles gel at a higher volume fraction, we propose a very simplified view based on the statistical hydrodynamic trapping of a particle by an another one in its neighborhood upon translation and during a short period of time. We show that the key parameter describing this hydrodynamic trapping varies as the cube of the average diameter and captures most features of the sol-gel transition. Finally, we pointed out that in the high shear limit the suspension viscosity is still closely related to electrostatic interactions and follows the same trends as the viscoelastic properties.     

关于“Programming with Semilocally Convex Function”(英文)

“ＰｒｏｇｒａｍｍｉｎｇｗｉｔｈＳｅｍｉｌｏｃａｌｙＣｏｎｖｅｘＦｕｎｃｔｉｏｎ”［１］一文对定义在局部星形集上的局部凸函数给出了二择一定理，并应用到约束最小化问题，得到了优化条件和共轭定理，本文用具体反例说明这些结果是错误的．     

Uranium oligomerization in chloride-based high temperature melts: in situ XAS studies

In situ EXAFS spectroscopic studies of uranium compounds in high temperature alkali chloride melts indicate the presence of oligomeric species. An investigation into UCl(3) and UCl(4) dissolved in LiCl reveals long range ordering of uranium atoms in the molten state which is not maintained on quenching. Studies of uranium dioxide dissolved in LiCl-KCl eutectic with HCl exhibit long range ordering in both molten and quenched states, and the EXAFS data can be modeled using multiple coordination shells.