SPE and determination by FAAS of heavy metals using a new synthesized polymer resin in various water and dried vegetables samples

Firstly, poly[phenyl thiadiazole methacrylamide-co-divinylbenzene-co-2-acrylamido-2-methylpropane sulfonic acid] (PTMAAm-co-DVB-co-AMPS), a new polymer resin was synthesized. This polymer resin was characterized by elemental analyzer, X-ray diffractometer, scanning electron microscope (SEM) and IR spectrometer. The glass column packed with the synthesized polymer resin was used for solid phase extraction (SPE). At the same time, the analytes were separated and preconcentrated from various water, dried vegetables samples and standard reference material (CRM) with SPE and determined by flame atomic absorption spectrometer (FAAS). The experimental conditions of this method such as pH, flow rates of sample, flow rates of eluent, type / concentration / volume of eluent, sample volume and matrix ions were examined. The limits of detection (µg L^?1) were calculated (3s) 0.9 for Mn(II), 1.4 for Cd(II), Co(II) and Zn(II), 1.5 for Cr(III), 2.2. for Cu(II), 1.9 for Pb(II),1.5 for Ni(II) and 1.9 for Fe(III) (n = 21). The low relative standard deviation, ≤ 2% (n = 11) and preconcentration factor as 75 for analytes were obtained.     

On-line preconcentration and determination of Au(III) in various environmental/industrial samples by flame atomic absorption spectrometry

A rapid and simple on-line method is described for the determination of Au(III) in various samples. The method is based on the sorption of gold(III) on Lewatit MonoPlus TP207 chelating resin including the iminodiacetate group, which is used as sorbent material and packed in a minicolumn. The chemical variables such as the pH of the sample solution, eluent type, interfering ions and concentrations of reagents, and instrumental variables such as sample loading volume, reagents flow rates, and tubing length, which affect the efficiency of the method were studied and optimised. Au(III) was sorbed on the chelating resin, from which it could be eluted with 3 mol L^?1 HCl, and then introduced directly to the nebuliser-burner system of FAAS. The limit of detection of the method was 0.2 µg L^?1 while the relative standard deviation was <4.0% for 20 µg L^?1 Au(III) concentration. The preconcentration factor was found to be 106 while the optimised sample volume was 15.3 mL. The accuracy of the method was verified by analysing the certified reference material. The developed method was applied successfully for the determination of gold in different samples with satisfactory results.     

Studies on Carbohydrates X. A New Method for the Preparation of Isopropylidene Saccharides

Cabohydrates reacting with acetone in the presence of molecular sieve and p—toluene sulfonic acid provided a simple, convenient, high yield and good selective process for preparation of isopropylidene carbohydrates.     

A new method for preparing TiO2 catalyst honeycombs without sintering

Composite catalyst honeycombs without sintering were prepared via kneading, mulling, extrusion molding, and solidifying at room temperature with the magnesite oxychloride gels modified by nano-rice husk ash (RHA) as a solidifying agent. The effects of nano-RHA and composite water-resistant agents on the water resistance of magnesite materials were studied. The solidification of the modified magnesite gels on TiO₂ catalyst honeycombs was analyzed. The experiments show that the proportional addition of nano-RHA markedly increases the water resistance of magnesite materials without reducing the bending strength, and the softening coefficient increases from 0.29 to 0.78. With further addiition of the complex water-resistant agents, the softening coefficient increases from 0.78 to 0.97. The optimal mass ratio of MgO in the solidifying agent to TiO₂ is 4:1, and the bending strength of unsintered catalyst honeycombs is 11.46 MPa. The desulfurization rate and denitration rate of this composite catalyst honeycomb on simulation smoke was 97 and 65 %, respectively, in 3 h.     

A mass‐fraction‐based interface‐capturing method for multi‐component flow

An interface‐capturing method based on mass fraction is developed to solve the Riemann problem in multi‐component compressible flow. Equations of mass fraction with modified form, which is derived from conservative equations of mass, are employed here to capture the interface. By introducing mass fraction into Euler equations system, as well as other conservative coefficients, a quasi‐conservative numerical model is created. Numerical examples show that the mass fraction model performs well not only in multi‐component fluids modeled by simple stiffened gas equation of state (EOS) but also in that modeled by complex Mie–Grüneisen EOS. Moreover, the mass fraction model is applied to Riemann problem with piecewise EOS; the expression of which depends on density. It is found that the mass fraction model can well adapt to the analytic change in piecewise EOS and produce accuracy solutions with fewer unknown quantities, and the model can be easily extended to m‐component fluid mixture by using only m + 4 equations with no additional conditions. Copyright © 2013 John Wiley & Sons, Ltd.     

Hydrothermal synthesis and characterization of NiS flower-like architectures

Under the influence of thiocyanate anions (SCN^?) and cetyltrimethyl ammonium bromide (CTAB), NiS flower-like architectures were successfully synthesized by a one-step hydrothermal method. The synthesized flower-like architectures, with a multilayered and highly ordered texture, have diameters of several micrometers. X-ray powder diffraction (XRD) shows that the NiS flower-like architectures are rhombohedral crystalline. On the basis of condition-dependent experiments, the diffusion-limited aggregation (DLA) model and cage effect were used to explain the growth process of rhombohedral crystalline NiS flower-like architectures. Magnetic measurements showed that the coercivity (H_c) of the as-obtained NiS flower-like architectures was 102.14 Oe.