Thermal analysis and X-ray studies of chiral ferroelectric liquid crystalline materials and their binary mixtures

Summary Thermal properties of a homologous series of ferroelectric liquid crystals S-(-)-[4-(2-n-alkoxy-propionyloxy)]biphenyl-4'-[n-alkoxy-(3,5-dimethyl)]benzoate have been investigated by polarizing optical microscopy and differential scanning calorimetry. The mesophases were identified and confirmed by X-ray too. Three binary mixtures were prepared from the individual homologues. In one of the mixtures (Mix1), the ferroelectric SmC* phase has broadened and became enantiotropic. This mesophase remained monotropic in the other two mixtures (Mix2, Mix3). The chiral nematic N* phase did not appear in Mix1, but remained monotropic for the other two mixtures. Two molecular parameters, the layer spacing and the average intermolecular distance have been calculated from the X-ray results for the homologues and their mixtures. An intercalated tail-to-tail packing of molecules was found both in the single compounds and their mixtures resulting in the layer spacing about half of the molecular length of the single compounds.     

Construction of Polycation‐Based Non‐Viral DNA Nanoparticles and Polyanion Multilayers via Layer‐by‐Layer Self‐Assembly

Summary: The multilayers of polycation‐based non‐viral DNA nanoparticles and biodegradable poly(L ‐glutamic acid) (PGA) were constructed by a layer‐by‐layer (LbL) technique. Poly(ethyleneimine) (PEI) was used to condense DNA to develop non‐viral DNA nanoparticles. AFM, UV‐visible spectrometry, and TEM measurements revealed that the PEI‐DNA nanoparticles were successfully incorporated into the multilayers. The well‐structured, easily processed multilayers with the non‐viral DNA nanoparticles may provide a novel approach to precisely control the delivery of DNA, which may have great potential for gene therapy applications in tissue engineering, medical implants, etc.

A TEM image of the cross section of a (PGA/PEI‐DNA nanoparticle)₂₀ multilayer.     

NARROW-DISPERSED CROSSLINKED CORE-SHELL POLYMER MICROSPHERES PREPARED BY SURFACE-INITIATED ATOM TRANSFER RADICAL POLYMERIZATION＊

Grafting of polystyrene with narrowly dispersed polymer microspheres through surface-initiated atom transfer radical polymerization (ATRP) was investigated. Polydivinylbenzene (PDVB) microspheres were prepared by dispersion polymerization with poly(N-vinyl pyrrolidone) (PVP) as stabilizer. The surfaces of PDVB microspheres were chloromethylated by chloromethyl methyl ether in the presence of zinc chloride as catalyst to form chloromethylbenzene initiating core sites for subsequent ATRP grafting of styrene using CuCl/bpy as catalytic system. Polystyrene was found to be grafted not only from the particle surfaces but also from within a thin shell layer, resulting in the formation of particles size increased from 2.38-2.58μm, which can further grow to 2.93μm during secondary grafting polymerization of styrene. This demonstrates that grafting polymerization proceeds through a typical ATRP procedure with living nature. All of the prepared microspheres have narrow particle size distribution with coefficient of variation around 10%.     

MICRO-PHASE SAEPARATION IN EPOXY RESIN WATERBORNE PARTICLES DURING CURING PROCESS

Sub-micron sized phenolic epoxy resin waterborne particles were prepared by phase inversion emulsification. Micro-phase separation occurred during the curing process at high temperature. The as-prepared samples possessed one glass transition temperature （Tg） and two exothermal processes during DSC heating scannings. After being thermally treated above the exothermal peak temperature, they possessed two glass transition temperatures with the disappearance of exothermal peaks, whilst a core/shell structure was formed. This was likely related with the outward diffusion of reactive oligomers to the outer layer of particles.     

Double Electric Layer on Liquid Sn-Ga Alloy in Acetonitrile Solutions of Electrolytes

The structure of the double electric layer (DEL) on a liquid dropping Sn-Ga electrode containing 8 at. % of Sn is studied in acetonitrile (AN) solutions of electrolytes. It is shown that the transition from aqueous to AN solutions of electrolytes makes it possible to expand the region of investigation of parameters of DEL on an Sn-Ga electrode from negative charges to a zero charge and to small positive charges. As follows from the obtained data, throughout the entire interval of charges studied, an excess, as compared with an Hg electrode, chemisorption interaction (Sn-Ga)-AN is absent. It is established that the distance of the closest approach of AN dipoles to an ionic core increases upon going from Hg to Sn-Ga to Ga. The Ga, Bi-Ga, and Sn-Ga electrodes, which possess close values of the “electrochemical work function,” are used as an example to show that the metal-solvent chemisorption interaction increases with decreasing distance of the closest approach of its dipoles to the ionic core of the metal. The effect of this factor becomes stronger as the donor number of the solvent increases.     

Sorption of Arsenic Oxyanions from Aqueous Solution on Goethite: a Study of Process Modelling

In the course of researching methods of sampling and monitoring toxic metals (as arsenic ions) in water and wastewaters, we selected the use of sorption for in-depth examination. Among other things, sorption modelling was investigated by the mechanism of surface complexation in order to describe the process or even predict the outcome for the expected rate, and in general, to develop this detection technique for pollutants. This investigation will include the application of goethite mineral as the suitable metal ion sorbent and the use of appropriate computer software. The relative thermodynamic aqueous speciation of the solution, in similar experimental conditions, was also studied.     

N-二氯乙酰基噁唑烷合成反应的薄层色谱法研究

用薄层色谱法监测了用二氯乙酰氯、醇胺和酮合成的除草剂的安全剂N 二氯乙酰基 口恶唑烷的反应过程。方法操作简便、快速、准确。     

Three-dimensional flow over a stretching surface in a viscoelastic fluid

This article looks at the hydrodynamic elastico-viscous fluid over a stretching surface. The equations governing the flow are reduced to ordinary differential equations, which are analytically solved by applying an efficient technique namely the homotopy analysis method (HAM). The solutions for the velocity components are computed. The numerical values of wall skin friction coefficients are also tabulated. The present HAM solution is compared with the known exact solution for the two-dimensional flow and an excellent agreement is found.     

Implicit meanflow–multigrid algorithms for Reynolds stress model computation of 3‐D anisotropy‐driven and compressible flows

The present paper investigates the multigrid (MG) acceleration of compressible Reynolds‐averaged Navier–Stokes computations using Reynolds‐stress model 7‐equation turbulence closures, as well as lower‐level 2‐equation models. The basic single‐grid SG algorithm combines upwind‐biased discretization with a subiterative local‐dual‐time‐stepping time‐integration procedure. MG acceleration, using characteristic MG restriction and prolongation operators, is applied on meanflow variables only (MF–MG), turbulence variables being simply injected onto coarser grids. A previously developed non‐time‐consistent (for steady flows) full‐approximation‐multigrid (s–MG) is assessed for 3‐D anisotropy‐driven and/or separated flows, which are dominated by the convergence of turbulence variables. Even for these difficult test cases CPU‐speed‐ups r_CPUSUP∈[3, 5] are obtained. Alternative, potentially time‐consistent approaches (unsteady u–MG), where MG acceleration is applied at each subiteration, are also examined, using different subiterative strategies, MG cycles, and turbulence models. For 2‐D shock wave/turbulent boundary layer interaction, the fastest s–MG approach, with a V(2, 0) sawtooth cycle, systematically yields CPU‐speed‐ups of 5±½, quasi‐independent of the particular turbulence closure used. Copyright © 2008 John Wiley & Sons, Ltd.     

Molecular Mixing and Flowfield Measurements in a Recirculating Shear Flow. Part I: Subsonic Flow

The mixing and flowfield of a complex geometry, similar to a rearward-facing step flow but with injection, is studied. A subsonic top-stream is expanded over a perforated ramp at an angle of 30°, through which a secondary stream is injected. The mass flux of the second stream is chosen to be insufficient to provide the entrainment requirements of the shear layer, which, as a consequence, attaches to the lower guidewall. Part of the flow is directed upstream forming a re-entrant jet within the recirculation zone that enhances mixing and flameholding. A control-volume model of the flow is found to be in good agreement with the variation of the overall pressure coefficient of the device with variable mass injection. The flowfield response to changing levels of heat release is also quantified. While increased heat release acts somewhat analogously to increased mass injection, fundamental differences in the flow behaviour are observed. The hypergolic hydrogen-fluorine chemical reaction employed allows the level of molecular mixing in the flow to be inferred. The amount of mixing is found to be higher in the expansion-ramp geometry than in classical free-shear layers. As in free-shear layers, the level of mixing is found to decrease with increasing top-stream velocity. Results for a similar configuration with supersonic flow in the top stream are reported in Part II of this two-part series.