Monte Carlo simulations on magnetic behavior of a spin-chain system in triangular lattice doped with antiferromagnetic bonds

A three-dimensional Ising-like model doped with anti-ferromagnetic (AFM) bonds is proposed to investigate the magnetic properties of a doped triangular spin-chain system by using a Monte-Carlo simulation. The simulated results indicate that a steplike magnetization behavior is very sensitive to the concentration of AFM bonds. A low concentration of AFM bonds can suppress the stepwise behavior considerably, in accordance with doping experiments on Ca₃Co₂O₆. The analysis of spin snapshots demonstrates that the AFM bond doping not only breaks the ferromagnetic ordered linear spin chains along the hexagonal c-axis but also has a great influence upon the spin configuration in the ab-plane.      

Self-Assembly of Micro-Parts onto Si Substrates at Liquid-Liquid Interface

We report a new approach for the self-assembly of cuboid micro-parts onto Si substrates to construct three-dimensional microstructures. To perform assembly, the Si substrates are prepared with a deep cavity array as binding sites. An aggregate composed of hundreds of uniformly aligned micro-parts is formed at the C10F18-H2O interface. The micro-parts are arranged by passing the substrate through the aggregate of micro-parts, thus the micro-parts are left on the substrate, and then the substrate is vibrated ultrasonically in the solution, making it possible for the micro-parts to fall into the cavities on the substrate. Finally the substrate is pulled out of the solution after assembly. This technique could give a high yield of up to 70%, providing a new method for micro-assembly.     

Further study of the viscoelastic phase separation of cyanate ester modified with poly(ether imide)

In this study, the viscoelastic phase separation process was studied further by time‐resolved light scattering, differential scanning calorimetry, and scanning electron microscopy in the system of poly(ether imide)‐modified bisphenol‐A dicyanate. It was observed that the evolution time of phase structure and relaxation time of diffusion flow of the bisphenol‐A dicyanate were similar with the phase diagram of curing conversion versus content of PEI. The results suggested that the viscoelastic phase separation was affected by the curing conversion of the system at the onset point of phase separation. © 2005 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 44: 517–523, 2006     

Chemoselective Catalytic Hydrogenation of α,β-Unsaturated Ketones and α,β-Unsaturated Carboxylic Esters

ＣｈｅｍｏｓｅｌｅｃｔｉｖｅＣａｔａｌｙｔｉｃＨｙｄｒｏｇｅｎａｔｉｏｎｏｆα，β┐ＵｎｓａｔｕｒａｔｅｄＫｅｔｏｎｅｓａｎｄα，β┐ＵｎｓａｔｕｒａｔｅｄＣａｒｂｏｘｙｌｉｃＥｓｔｅｒｓＺＨＡＮＧＪｉｎｇ－ｗｅｎ＊，ＺＨＡＯＪｉａｎ－ｚｈａｎｇ，Ｚ...     

Semilinear Differential Inclusions in Separable Banach Spaces

Ｓｅｍｉｌｉｎｅａｒ　Ｄｉｆｆｅｒｅｎｔｉａｌ　Ｉｎｃｌｕｓｉｏｎｓ　ｉｎ　Ｓｅｐａｒａｂｌｅ　Ｂａｎａｃｈ　ＳｐａｃｅｓＸｕｅＸｉｎｇｍｅｉ（薛星美）ａｎｄＳｏｎｇＧｕｏｚｈｕ（宋国柱）（ＤｅｐａｒｔｍｅｎｔｏｆＭａｔｈｅｍａｔｉｃｓ，Ｎａｎｊｉｎ...     

激光二极管泵浦的高重复频率Nd：YAG激光器

报道两个１．５Ｗ连续激光二极管端面泵浦的声光调ＱＮｄ：ＹＡＧ激光器，输出激光脉冲的最高重复频率为３０ｋＨｚ重复频率１ｋＨｚ时，最窄脉宽为１２ｎｓ，最高峰值功率为１２．１ｋＷ。     

新型稀土电子输运材料Tb(AcA)3·phen

Kido等人在文献[1]中报导,在研究有机电致发光(OEL)器件时发现,斓系化合物不能很好地传输载流子.但是,我们在实验中却现Tb(AcA)3phen·不仅是一种很好的OEL发射材料.而且具有很强的电子输运能力.     

Renormalization group calculation of the critical temperature dependence on longitudinal magnetic field for a disordered superconductor model

We describe a calculation ofT _c (P, H) in a model of a disordered superconductor which is based on the de Gennes-Skal-Shklovskii (dGSS) picture of the large cluster in a percolation system. The calculation is done by carrying out successive decimations on the Landau-Ginzburg Hamiltonian describing the links in the model. We calculateT _c (P, H) in the presence of longitudinal magnetic field by evaluating the renormalized Landau-Ginzburg coupling when the renormalized Landau-Ginzburg length equals the percolation link length in the dGSS picture and obtain the approximate analytic form ofT _c (P, H).Work supported by China Natural Science Foundation     

Thermodynamic properties of aqueous mixtures of LiCl and Li2SO4 at different temperatures

Emf measurements were made on the cell without liquid junction: Li?ISE LiCl(m₁), Li₂SO₄(m₂) Ag/AgCl. The performances of the electrode pairs constructed in our laboratory were tested and exhibited near-Nernstian behavior. The mean activity coefficients of LiCl for the system Li⁺?Cl^??SO ₄ ^2? ?H₂O have been investigated by the emf values at temperatures of 0, 15, 35°C and constant total ionic strengths of 0.05, 0.1, 0.5, 1.0, 2.0, 3.0 and 5.0 mol·kg^?1. The activity coefficients decrease with increasing temperature and the ionic strength fraction of Li₂SO₄ in the mixtures. The thermodynamic properties are interpreted by use of Harned's empirical equations and Pitzer's ion interaction approach including the contribution of higher order electrostatic terms. The experimental results obey Harned's rule and are described by using Pitzer equations satisfactorily. The activity coefficients of Li₂SO₄, the osmotic coefficients and the excess free energies of mixing for the system in the experimental temperature range were reported.