A coincidence technique for the study of intense laser atom interactions

A new device for charged particle coincidence experiments in strong-field, short pulse laser-atom/molecule interactions is presented. The device consists of a single time of flight spectrometer, common for both positive and negative charge detection. Experimental parameters required for the use of the device in the high intensity regime are discussed. A demonstration of electron-ion coincidence measurements in the interaction of Xe atoms with 60 fs laser pulses at 800 nm and an intensity of W/cm² is reported. Received 22 November 1999     

Filler effect on photopolymerization of a medical oligoester composition

The effect of an inorganic filler (aerosil) on photopolymerization of an oligoester composition is investigated by means of IR spectroscopy. It is shown that the filler, depending on its concentration, is capable of enhancing or hindering the main process, or inducing side reactions. Institute for Surface Chemistry, National Academy of Sciences of Ukraine, 31, Nauka Ave., Kiev, 252022, Ukraine. Translated from Zhurnal Prikladnoi Spektroskopii, Vol. 66, No. 1, pp. 119–124 January–February, 1999.     

Growth and field emission property of coiled carbon nanostructure using copper as catalyst

Coiled carbon nanostructure (CNS) is prepared by a catalytic chemical vapor deposition (CVD) process on copper/chromium films deposited by radio frequency (RF) sputtering. Uniform CNS with coiled structure is fabricated by changing the size of the catalyst particles. The effects of Cu catalyst size and RF sputtering power, on the growth of the coiled CNS are discussed, and the results importantly conclude that Cu-catalyzed CVD offers a preferable control of coiled CNS to optimize the field emission property for application.     

分散化供应链的自组织演化机制建模与仿真

供应链是一个复杂适应系统.提出了分散化供应链演化的自组织机制.在开放结构下,多企业主体为了适应外部环境,在非线性互动中涌现出供应链协作结构和协调模式.借鉴生物系统环境适应能力思想,建立了分散化供应链自组织演化模型,并采用Multi-agent技术进行仿真,证明了分散化供应链的自组织演化机制.外部环境和企业内部机制因素控制着分散化供应链的演化,其演化对初始条件高度敏感,存在着锁定、路径依赖和混沌等自组织系统特性.     

Rational approximation to trigonometric operators

We consider the approximation of trigonometric operator functions that arise in the numerical solution of wave equations by trigonometric integrators. It is well known that Krylov subspace methods for matrix functions without exponential decay show superlinear convergence behavior if the number of steps is larger than the norm of the operator. Thus, Krylov approximations may fail to converge for unbounded operators. In this paper, we propose and analyze a rational Krylov subspace method which converges not only for finite element or finite difference approximations to differential operators but even for abstract, unbounded operators. In contrast to standard Krylov methods, the convergence will be independent of the norm of the operator and thus of its spatial discretization. We will discuss efficient implementations for finite element discretizations and illustrate our analysis with numerical experiments. AMS subject classification (2000)  65F10, 65L60, 65M60, 65N22     

Measurement of excitation spectra for highly ionized sulphur

The excitation spectra in the wavelength range of 19—40 nm for highly ionized sulphur ions were measured by using the beam-foil method at the Heavy lon Research Facility in Lanzhou. In this experiment, more than 30 spectral lines were observed, which belonged to the transitions of the excitation energy levels for highly ionized SX—SXV ions, and 5 new lines were determined. The experimental results were compared with those from other experiments and theoretical calculations.     

Adsorption of TTF,TCNQ and TTF-TCNQ on Au(111):An in situ ECSTM study

The adsorption and adlayer structures of tetrathiofulvalene (TTF), tetracyanoquinodimethane (TCNQ) and TTF-TCNQ on Au(111) have been systematically investigated by in situ electrochemical scanning tunneling microscopy (ECSTM) and cyclic voltammetry in 0.1 mol?L?1 HClO4. All the three molecules were found to form well-ordered adlayers in the double-layer potential region of Au(111). For TTF and TCNQ adlayers, (6×3) and (4×7) structures have been observed, respectively. A structural transition was observed on...     

Control of the microstructure of polymer network and effects of the microstructures on light scattering properties of UV‐cured polymer‐dispersed liquid crystal films

Polymer‐dispersed liquid crystals (PDLC) films were prepared from ultraviolet (UV) irradiation‐induced polymerization of the photopolymerizable monomers in photopolymerizable monomers/nematic liquid crystal (LC) mixtures. The effects of the composition of the mixtures, the curing temperature, and the UV light intensity on the microstructure of the polymer network in the PDLC films were investigated. Furthermore, the effects of the microstructures on the light scattering properties of the PDLC films in the wavelength region of 300–2500 nm were studied experimentally and theoretically based on the combination of three kinds of classical light scattering theories: the Rayleigh‐Gans (RG) approach, the anomalous diffraction (AD) approach, and the geometrical optics (GO) approach. It was found that the sizes of LC domain in PDLC films increased with the increase of the LC content as well as the decrease of the UV curing intensity, while increased at first and then decreased with the increase of the curing temperature. Moreover, smaller LC domain sizes could exhibit strong scattering properties in a smaller VIS wavelength region and the transmittance in NIR region (especially in the wavelength range of 1300–2500 nm) obviously decreased with the increasing sizes of LC domain. © 2008 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 46: 2090–2099, 2008     

Branched polymer via free radical polymerization of chain transfer monomer: A theoretical and experimental investigation

A simple mathematic model for the free radical polymerization of chain transfer monomers containing both polymerizable vinyl groups and telogen groups was proposed. The molecular architecture of the obtained polymer can be prognosticated according to the developed model, which was validated experimentally by homopolymerization of 4‐vinyl benzyl thiol (VBT) and its copolymerization with styrene. The chain transfer constant (C_T) of telogen group in a chain transfer monomer is considered to play an important role to determine the architecture of obtained polymer according to the proposed model, either in homopolymerization or copolymerization. A highly branched polymer will be formed when the C_T value is around unity, while a linear polymer with a certain extent of side chains will be obtained when the C_T value is much bigger or smaller than unity. The C_T of VBT was determined to be around 15 by using the developed model and ¹H NMR monitored experiments. The obtained poly(VBT) and its copolymers were substantiated to be mainly consisted of linear main chain with side branching chains, which is in agreement with the anticipation from the developed model. The glass transition temperature, number average molecular weight, and its distribution of those obtained polymer were primarily investigated. This model is hopefully to be used as a strategy to select appropriate chain transfer monomers for preparing hyperbranched polymers. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 1449–1459, 2008     

Effect of molecular weight of macro‐iniferter on electro‐optical properties of polymer dispersed liquid crystal films prepared by iniferter polymerization

Polymer dispersed liquid crystal (PDLC) films were prepared by a devised method, in which photo‐polymerization induced phase separation in a mixtures of a macro‐iniferter, methyl acrylater, and liquid crystal. The morphology of the obtained PDLC films was examined on a polarized optical microscopy, and the effect of molecular weight of MIs on the electro‐optical properties was deliberately investigated. Decreasing the molecular weight of MIs in the films led to formation of larger liquid crystal droplets and a lower V_th values. V_sat increased and the memory effect decreased because of the increased interface anchoring strength induced by the higher molecular weight of polymer matrices. © 2009 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 47: 1530–1534, 2009