Breakdown of a gas gap in a surface barrier discharge

The processes that occur in a surface barrier discharge in oxygen at atmospheric pressure have been studied by numerical modeling. Modeling is performed assuming the existence of local equilibrium, and the dynamics of charged particles in the gas gap is calculated using continuity equations. The configuration of the electric field in the discharge zone is determined by integration of the Poisson equation. It turns out that the breakdown of the gas gap is determined by the photoemission from the cathode surface. The appearance and development of the microdischarge channel are sustained by the cathode layer that is formed at the conducting cathode. The parameters of the cathode layer obtained in oxygen at atmospheric pressure are virtually the same as for the ordinary cathode layer of the glow discharge.     

Sedimentation of a composite particle in a spherical cavity

The boundary effect on the sedimentation of a colloidal particle is investigated theoretically by considering a composite sphere, which comprises a rigid core and an ion-penetrable membrane layer, in a spherical cavity. A pseudo-spectral method is adopted to solve the governing electrokinetic equations, and the influences of the key parameters on the sedimentation behavior of a particle are discussed. We show that both the qualitative and quantitative behaviors of a particle are influenced significantly by the presence of the membrane layer. For example, if the membrane layer is either free of fixed charge or positively charged and the surface potential of the rigid core is sufficiently high, the sedimentation velocity has a local minimum and the sedimentation potential has a local maximum as the thickness of the double layer varies. These local extrema are not observed when the membrane layer is negatively charged. If the double layer is thin, the influence of the fixed charge in the membrane layer on the sedimentation potential is inappreciable.     

Relaxation dynamics of a polymer in a 2D confinement

The molecular dynamics of oligomeric poly(propylene glycol) (PPG) liquids (MW=1000, 2000, and 4000 g/mol) confined in a two-dimensional layer-structured Na-vermiculite clay has been studied by broadband dielectric spectroscopy. The alpha-relaxation and the normal mode relaxation processes were studied for all samples in bulk and confinement. The most prominent experimental observation was that for the normal mode process: the relaxation rate in the clay is drastically shifted to lower frequencies compared to that of the bulk material. This slowing down is probably caused by the strongly reduced number of accessible chain conformations in two dimensions. Also the temperature dependence of the relaxation time for the normal mode process is strongly affected by the confinement. In contrast, for the alpha-relaxation of the confined polymers we observed only a slight increase of the relaxation rate at high temperatures compared to the corresponding bulk samples, and a decrease of its relaxation strength relative to the beta relaxation. Thus, the glass transition is unaffected by the 2D confinement, suggesting that the underlying phenomena responsible for the glass transition is the same as in bulk. Moreover, in the clay the intensity of the normal mode is stronger than that of the alpha-process, in contrast to the bulk samples where the opposite behavior is observed.     

Critical shift of a confined fluid in a nanopore

In a van der Waals model for a non-wetting confined fluid in a nanopore a shift in the critical temperature, with respect to the bulk value, is predicted. The agreement with experiment is good, giving that the characterization of fluids is done only by the Lennard–Jones potential parameters. The theory gives also a similar shift in the critical pressure.     

Electrophoresis of a membrane-coated sphere in a spherical cavity

The boundary effect on the electrophoresis of particles covered by a membrane layer is discussed by considering a spherical particle in a spherical cavity under the conditions where the effect of double-layer polarization can be significant. The influence of the key parameters of the system under consideration on the electrophoretic mobility of a particle is investigated. These include the surface potential; the thickness of the double layer; the relative size of the cavity; and the thickness, the fixed charge density, and the friction coefficient of the membrane layer. The fixed charge in the membrane layer of a particle is found to have a significant influence on its electrophoretic behavior. For instance, depending upon the amount of fixed charge in the membrane layer, the mobility of a particle may exhibit a local minimum as the thickness of the double layer varies.     

Wetting of a particle in a thin film

When a particle is placed in a thin liquid film on a planar substrate, the liquid either climbs or descends the particle surface to satisfy its wetting boundary condition. Analytical solutions for the film shape, the degree of particle immersion, and the downward force exerted by the wetting meniscus on the particle are presented in the limit of small Bond number. When line tension is significant, multiple solutions for the equilibrium meniscus position emerge. When the substrate is unyielding, a dewetting transition is predicted; that is, it is energetically favorable for the particle to rest on top of the film rather than remain immersed in it. If the substrate can bend, the energy to drive this bending is found in the limits of slow or rapid solid deflection. These results are significant in a wide array of disciplines, including controlled delivery of drugs to pulmonary airways, the probing of liquid film/particle interface properties using particles affixed to AFM tips and the positioning of small particles in thin films to create patterned media.     

Mechanically regulated rotation of a guest in a nanoscale host

The spinning rate of an encapsulated cyclophane guest is affected by the "size" of the coguests.     

Alignments of a Microparticle Pair in a Glow Discharge

Stability of a vertically aligned microparticle pair in a stratified glow DC discharge is experimentally investigated. Using laser perturbations, it is shown that, for the same discharge parameters, a pair of microparticles can be suspended in two stable configurations: vertical and horizontal. The interparticle interaction and the electric field of the stratum in the region of particle levitation are quantitatively investigated for the first time. The decharging effect of the lower (downstream) particle by the ion flow wake is also observed for the first time in a glow discharge. The obtained experimental data made it possible to check the analytical criteria for the configurational stability of the system.     

Synthesis of a paraffin phase change material microencapsulated in a siloxane polymer

The coemulsification method suitable for the formulation of microcapsules of n-eicosane coated with a polysiloxane is developed. This method allows to synthesize core–shell microcapsules of paraffin which have the shape of spheres or distorted spheres and are designed for the use as phase change materials. The microcapsules are formed in aqueous phase by the precipitation of n-eicosane together with modified polyhydromethylsiloxane from a common solvent which is miscible with aqueous media. The polysiloxane is modified by the attachment of silylvinyl and alkoxy functions before coemulsification with the paraffin. It also contains the Pt(0) Karstedt catalyst. The microcapsules formed by coemulsification are stabilized by the in situ cross-linking of the polysiloxane shell. The shell is additionally modified by the in situ generation of silanol groups which provide colloidal stabilization of microspheres in aqueous phase. Microcapsules were studied by DSC, SEM, optical polarized microscope, and by thermooptical analysis (TOA).     

Implementation of a quality system in a clinical laboratory

The effects of a quality system are measured with the aid of quality indicators, which can be used for both decision-making by the management of the laboratory and for process control. The need for economic appraisal is stressed since the development of a quality system is very time- and labour-consuming. The aspects of both the customer and the personnel involved should be considered to evaluate the quality system. It is also important to define practical means to build up and maintain a quality system especially in smaller laboratories. For instance, simple tools to evaluate uncertainty of measurement and availability of inexpensive national reference materials are needed.     

Location of a branch in a saturated carbon chain

Oxidative degradation by chromic acid in glacial acetic acid has been developed as an effective method for location of a branch in a saturated carbon chain. Detection of cleavage products by use of gas phase chromatography allows convenient application of the method to samples of 3–10 mg. Several branched-chain acids and a branched-chain hydrocarbon have been found to yield the expected cleavage products; however, selective attack on a branch located alpha, beta or gamma to carboxyl is not significant. The mechanism of the oxidation and the protective influence of carboxyl are discussed.     

两嵌段共聚高分子链通过薄膜上纳米孑孔隙输运的研究

针对两嵌段高分子链的跨膜输运过程,分别给出与不同输运次序相对戍的高分子链的自由能,进而通过求解Fokker-Planck方程并在不同条件下对平均首次通过时间进行了数值计算.计算结果表明,当共聚高分子链由良溶剂区向不良溶剂区输运时,不能发生线团一链滴转变的链首先输运总是有利于整个高分子链的输运.而在给定输运次序的情况下,化学势、线团一链滴转变、共聚链的组成以及输运速率等因素对输运时间可产生显著影响.相关研究结果可为调控实际生物高分子链的输运时间提供可能的理论线索.     

Monte Carlo simulation of a polymer-analogous reaction in a polymer blend

The autocatalytic polymer-analogous reaction A → B in a blend composed of two contacting layers of compatible homopolymers A and B is studied by numerical simulation using the dynamic continuum Monte Carlo method. The evolution of the numerical density of units A and units initially belonged to the chains of homopolymer A is investigated in the course of the reaction and interdiffusion. Local characteristics of the distribution of the homopolymer with respect to its composition and blocks A and B with respect to their length are calculated at different times. The dispersions of the above distributions are appreciably higher than the corresponding dispersion of the Bernoullian copolymer of the same average composition, despite the random character of the reaction. This effect can be provided by changes in the composition of the blend on the scale of the reacting chain as well as by the diffusive mixing of the above chains. For the products of the polymer-analogous reaction, the broadening of the compositional distribution is predicted also by the theoretical model, which describes interdiffusion in the reacting system on scales that are markedly greater than the size of a polymer chain.     

Quantum dynamics of a charged particle in a penning trap

With the help of the exact classical path representation of the time dependent propagator the dynamics of a charged particle in a Penning trap in the presence of an additional classical, time-dependent electric field is investigated. In this way the connection between quantum and classical dynamics is exhibited in a clear way. The possibility of localizing a particle in the ground state of a Penning trap with unit probability by a suitably chosen electric field is discussed.     

Electrical conduction in composites of a TCNQ anion-radical salt in a polymer matrix

The conduction behavior of composites of the anion-radical salt NaTCNQ (sodium 7,7,8,8-tetracyanoquinodimethanide) in poly(vinyl chloride) plasticized by polyurethane has been studied. TCNQ salt-polymer composites that have good moldability and flexibility are characterized by molecular or granular dispersion of the TCNQ salt in a polar polymer matrix. The conduction mode changes from one due to molecularly dispersed sites (CMDS) to one due to granularly dispersed sites (CGDS) with increasing NaTCNQ content. In the CMDS region, the predominant conduction is ionic; TCNQ anion-radicals migrate toward the anode under a dc biasing voltage and a high-resistivity layer is formed near the cathode. The fixation of TCNQ salt at sites in the polymer matrix is believed to be important for the stabilization of electronic conduction under a dc electric field. In the CGDS region, the conduction is electronic and the current-voltage characteristics of the composite are nonohmic, which indicates that carrier generation depends on the Poole-Frenkel effect.     

The short-time self-diffusion coefficient of a sphere in a suspension of rigid rods

The short-time self-diffusion coefficient of a sphere in a suspension of rigid rods is calculated in first order in the rod volume fraction phi. For low rod concentrations, the correction to the Einstein diffusion constant of the sphere due to the presence of rods is a linear function of phi with the slope alpha proportional to the equilibrium averaged mobility diminution trace of the sphere interacting with a single freely translating and rotating rod. The two-body hydrodynamic interactions are calculated using the so-called bead model in which the rod of aspect ratio p is replaced by a stiff linear chain of touching spheres. The interactions between spheres are calculated using the multipole method with the accuracy controlled by a multipole truncation order and limited only by the computational power. A remarkable accuracy is obtained already for the lowest truncation order, which enables calculations for very long rods, up to p=1000. Additionally, the bead model is checked by filling the rod with smaller spheres. This procedure shows that for longer rods the basic model provides reasonable results varying less than 5% from the model with filling. An analytical expression for alpha as a function of p is derived in the limit of very long rods. The higher order corrections depending on the applied model are computed numerically. An approximate expression is provided, valid for a wide range of aspect ratios.     

Optical dephasing in a glass-like system: a photon echo study of pentacene in benzoic acid

Optical absorption and picosecond photon echo experiments are used to study the dephasing of pentacene in benzoic acid. It is shown that, while the absorption spectrum of pentacene is effected by proton transfer in the benzoic acid dimer, the dephasing is caused by elastic and inelastic phonon scattering processes.     

Plateau instability of a liquid crystalline cylinder in a magnetic field

The capillary instability of a liquid crystalline cylinder in magnetic field is considered using an energy approach. The boundary problem is solved in the linear approximation of the anisotropy chi(a) of the magnetic susceptibility chi. The effect of anisotropy, in the region 1> chi > chi(a) > chi2, can be strong enough to counteract and even reverse the tendency of the field to enhance stabilization by enlarging the cutoff wave number k(s) beyond the conventional one set by Rayleigh.     

Controlling photochemical geometric isomerization of a stilbene and dimerization of a styrene using a confined reaction cavity in water

Utility of a water-soluble deep cavity cavitand, octa acid, as a reaction medium is illustrated by carrying out photochemical reactions of a stilbene and a styrene included within the octa acid in water. Geometric isomerization of trans-4,4'-dimethyl stilbene is restricted while dimerization of 4-methyl styrene is facilitated within the octa acid cavity. The excited-state chemistry of both systems is different in this medium from that in organic solvents. The change in chemistry is attributed to the supramolecular effects provided by the host cavity.