Hall effects and entropy generation applications for peristaltic flow of modified hybrid nanofluid with electroosmosis phenomenon

The electroosmotic peristaltic flow of modified hybrid nanofluid in presence of entropy generation has been presented in this thermal model. The Hall impact and thermal radiation with help of nonlinear relations has also been used to modify the analysis. The assumed flow is considered due to a non-uniform trapped channel. The properties of modified hybrid nanofluid model are focused with interaction of three distinct types of nanoparticles namely copper ($Cu)$, silver ($Ag$) and aluminum oxide ($A{l}_2{O}_3).$ The mathematical modeling and significances of entropy generation and Bejan number are identified. With certain flow assumptions, the governing equations are attained for optimized peristaltic electroosmotic problem. Widely used assumptions of long wave length and low Reynolds number reduced the governing equations in ordinary differential equations. The ND solver is flowed for the solution process. The physical significant of results is observed by assigning the numerical values to parameters.     

Electrochemical vapor generation of selenium species after online photolysis and reduction by UV-irradiation under nano TiO<Subscript>2</Subscript> photocatalysis and its application to selenium speciation by HPLC coupled with atomic fluorescence spectrometry

An online UV photolysis and UV/TiO₂ photocatalysis reduction device (UV–UV/TiO₂ PCRD) and an electrochemical vapor generation (ECVG) cell have been used for the first time as an interface between high-performance liquid chromatography (HPLC) and atomic fluorescence spectrometry (AFS) for selenium speciation. The newly designed ECVG cell of approximately 115 L dead volume consists of a carbon fiber cathode and a platinum loop anode; the atomic hydrogen generated on the cathode was used to reduce selenium to vapor species for AFS determination. The noise was greatly reduced compared with that obtained by use of the UV–UV/TiO₂ PCRD–KBH₄–acid interface. The detection limits obtained for seleno-DL-cystine (SeCys), selenite (Se^IV), seleno-DL-methionine (SeMet), and selenate (Se^VI) were 2.1, 2.9, 4.3, and 3.5 ng mL^–1, respectively. The proposed method was successfully applied to the speciation of selenium in water-soluble extracts of garlic shoots cultured with different selenium species. The results obtained suggested that UV–UV/TiO₂ PCRD–ECVG should be an effective interface between HPLC and AFS for the speciation of elements amenable to vapor generation, and is superior to methods involving KBH₄.     

Surface patterns of block copolymers in thin layers after vapor treatment

A systematic study of formation of surface patterns in block copolymer thin layers after their exposure to solvent vapors was performed. The studied effect involves layers of thickness approximately equal to the ordering size of polymers - about 45 nm. Experiments were performed on three styrene - methacrylate derivative block copolymers, synthesized by living anionic polymerization: poly(4-octylstyrene)-block-poly(butyl methacrylate), poly(4-fluorostyrene)-block-poly(butyl methacrylate) and poly(p-octylstyrene)-block-poly(methyl methacrylate). The polymers were exposed to vapors of chloroform, 1,4-dioxane, hexane, acetone and tetrahydrofuran.     

Comparison between the pervaporation and vapor permeation performances of polycarbonate membranes

The pervaporation and vapor permeation performance of symmetrical and asymmetrical polycarbonate membranes, prepared via a dry-phase inversion and wet-phase inversion methods, respectively, were studied by measuring the permeation rate and separation factor. It was found that the polymer concentration effect on the pervaporation performance for the symmetrical polycarbonate membrane was lower than that for the asymmetrical polycarbonate membrane. Compared with pervaporation, vapor permeation has a significantly increased separation factor with a decreased permeation rate for the symmetrical polycarbonate membrane. Water molecules preferentially dissolve into the symmetrical polycarbonate membrane and diffuse easily through the membrane.     

Application of correlation-gas chromatography to evaluate the vaporization enthalpy of a component in an equilibrium mixture

The vaporization enthalpies and vapor pressures of acetoin, ethyl 3-hydroxybutyrate and ethyl 3-hydroxyhexanoate, found in a variety of foods and flavors, are evaluated at T = 298.15 K using correlation-gas chromatography; values of (48.7 ± 0.4), (55.9 ± 0.6) and (61.9 ± 0.6) kJ mol⁻¹, respectively, were obtained. These values are in good agreement with estimated values. Vapor pressures of the standards as a function of temperature were also used to calculate vapor pressures of the target compounds and all resulting data were fit to second order polynomials. These polynomials were then used to predict boiling temperatures of both standards and target substances. Agreement with experimental boiling temperatures was generally within 10 K suggesting that vapor pressures are accurate to within a factor of two. Acetoin exists as an equilibrium mixture of monomer and dimer. This report provides an example of the utility of using correlation-gas chromatography to obtain thermochemical data on an impure material.     

Selective pre-concentration of selenite from aqueous samples using mercapto-silica

Silica gel modified with 3-mercaptopropyl-trimethoxysilane was used for the selective separation and pre-concentration of selenite (Se(IV)) from aqueous solutions containing Se(IV) and selenate (Se(VI)). Over a wide range of acidity, from 2 mol l⁻¹ HCl to pH 9.00, Se(IV) was taken up by the mercaptopropyl-silica with nearly 100% efficiency; Se(VI) however was unretained. Se(IV) content was determined by hydride generation atomic absorption spectrometry (HGAAS), following batch release of the selenium from the pre-concentration medium by acidic periodate. The overall pre-concentration efficiency, including both take-up and elution, in the range of 89-106%. The method was applied to spiked seawater samples containing as low as 800 ng l⁻¹ Se in selenite form. This solid-phase extraction system offers several major advantages over conventional solvent extraction procedures. It firstly exhibits high selectivity for Se(IV) over Se(VI). Using the solid-phase media, pre-concentration of Se(IV) in dilute water samples can be carried out in the field, stabilizing the selenite-selenium in a convenient form for transport and storage. In addition, selenium stored on silica is derived solely from Se(IV) overcoming problems of selenium redox speciation changes and loss during storage.     

气相渗透法中的溶质吸附效应

在气相渗透仪上，用四个低分子量有机化合物和五个已知平均分子量的窄分布聚苯乙烯低聚体，对ＶＰＯ方法中的溶质吸附效应作了研究，提出了一种对吸附效应作改正的方法．所得结果表明，在扣除溶质吸附效应后，仪器常数Ｋ无分子量依赖性，提高了测定低分子量聚合物数均分子量的准确性．     

Determination of tin in soil by continuous hydride generation and inductively coupled plasma mass spectrometry

A method was investigated for the determination of Sn in soil samples by KOH fusion followed by continuous hydride generation coupled with inductively coupled plasma mass spectrometry (HG-ICP-MS). Sample solutions in 3.0 M HCl were mixed in line with a solution of 2.4% NaBH₄ and 0.25 M KOH to generate stannane gas. The mixture was delivered continuously to a gas/liquid separator and the stannane gas was introduced into a Perkin-Elmer Sciex Elan 6000 ICP-MS for concentration measurements. A method detection limit of 0.45 mg/kg was sufficient for Sn levels commonly found in soil samples. Sn concentrations as low as 2.5 mg/kg were reproducibly measured in soil samples. Sample results by HG-ICP-MS agreed within ±17% relative difference to results by instrumental neutron activation analysis (INAA) and within ±6% relative difference to results by KOH fusion followed by inductively coupled plasma optical emission spectroscopy (ICP-OES).     

Molecular origins of the remarkable chiral sensitivity of second-order nonlinear optics.

Recent observations of remarkably large chiroptical effects in second-harmonic generation (SHG) and sum-frequency generation (SFG) measurements suggest exciting possibilities for the development of new chiral-specific spectroscopies and novel chiral materials for nonlinear optics. Several fundamental studies designed to elucidate the molecular and macromolecular origins of the chiral responses are reviewed to provide a framework for development of this emerging field. In general, the chiral activity in SHG and SFG has the potential to arise from complex interactions between hosts of different competing effects. Fortunately, relatively simple electric dipole-allowed mechanisms routinely dominate the nonlinear optical chiral activities of most practical systemsexpressions can often be generated to link the. This substantial reduction in complexity allows for the development of simple models connecting the macroscopic nonlinear optical response to intuitive molecular and supramolecular properties.     

Hyphenation of flow injection/sequential injection with chemical hydride/vapor generation atomic fluorescence spectrometry

The dominant role played by flow injection/sequential injection (FI/SI, including lab-on-valve, LOV) in automatic on-line sample pretreatments coupling to various detection techniques is amply demonstrated by the large number of publications it has given rise to. Among these, its hyphenation with hydride/vapor generation atomic fluorescence spectrometry (HG/VG-AFS) has become one of the most attractive sub-branches during the last years, attributed not only to the high sensitivity of this technique, but also to the superb separation capability of hydride/vapor forming elements from complex sample matrices. In addition, it also provides potentials for the speciation of the elements of interest.It is worth mentioning that quite a few novel developments of sample pretreatment have emerged recently, which attracted extensive attentions from the related fields of research. The aim of this mini-review is thus to illustrate the state-of-the-art progress of implementing flow injection/sequential injection and miniaturized lab-on-valve systems for on-line hydride/vapor generation separation and preconcentration of vapor forming elements followed with detection by atomic fluorescence spectrometry, within the period from 2004 up to now. Future perspectives in this field are also discussed.