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Several Experimental Parameters (several + experimental_parameter)
Selected AbstractsCrinkling Ultralong Carbon Nanotubes into Serpentines by a Controlled Landing ProcessADVANCED MATERIALS, Issue 41 2009Yagang Yao Serpentine carbon nanotubes (CNTs) are successfully synthesized by controlling the landing of ultralong CNTs on a quartz surface. Several experimental parameters are investigated and the growth mechanism is further clarified (see figure). It is demonstrated that the high on/off ratio of single CNTs is maintained when serpentine CNTs are used to produce ultrahigh-current CNT-based devices. [source] Synthesis of lauryl methacrylate star-like polymers via ATRPASIA-PACIFIC JOURNAL OF CHEMICAL ENGINEERING, Issue 5 2009Lei Qiu Abstract Lauryl methacrylate (LMA) star-like polymers were synthesized by atom transfer radical polymerization (ATRP) using the ,arm-first' method. Linear poly lauryl methacrylate (PLMA) precursors were firstly prepared with ethyl ,-bromoisobutyrate (EBriB) as initiator and cuprous chloride (CuCl)/N,N,N,,N,,N,-pentamethyldiethylenetriamine (PMDETA) as catalyst in cyclohexanone via ATRP, and subsequently used as macromolecule initiator(MI) to synthesize star polymers in the presence of cross-linker ethylene glycol dimethacrylate (EGDMA). Several experimental parameters, such as the PLMA arm length, the ratio of MI to cross-linker, the addition amount and moment of cross-linker and the reaction time for the star formation were systematically investigated. The samples were removed at regular intervals and analyzed by gel permeation chromatography (GPC) to track Mn and Mw/Mn of star-like polymer, by which the influence of the experimental parameters on the structures of the star-like polymers was studied. Employing shorter arm lengths and more cross-linker could produce star-like polymers with higher molecular weight and more arms per star. Copyright © 2009 Curtin University of Technology and John Wiley & Sons, Ltd. [source] Development of a new method for analysis of Sudan dyes by pressurized CEC with amperometric detectionELECTROPHORESIS, Issue 11 2007Shaofeng Liu Abstract A new analytical method, pressurized CEC (pCEC) with amperometric detection (AD) using 1.5,,m RP nonporous silica packed columns has been developed for the rapid separation and determination of four Sudan dyes in hot chilli. The influence of several experimental parameters on the retention behavior has been investigated. The electrochemical oxidation of Sudans I,IV separated by pCEC can be reliably monitored with a carbon electrode at +0.95,V (vs. Ag/AgCl). Fast and efficient separation of the analytes was achieved within 7,min by pCEC under the optimum conditions with an ACN/water (95:5%) mobile phase containing formic acid (pH,4.3), 5% acetone and 0.002% triethylamine using a separation voltage of 12,kV. The detection limits for four Sudan dyes ranged from 8.0,×,10,7 to 1.2,×,10,6,mol/L. To evaluate the feasibility and reliability of this method, the proposed pCEC-AD method was further demonstrated with hot chilli samples spiked with Sudan dyes. [source] Small molecule adsorption on to polyester capillary-channeled polymer fibers: Frontal analysis of naphthalene and naphthol (naphthalene and naphthol adsorption on capillary-channeled polymer fibers)JOURNAL OF SEPARATION SCIENCE, JSS, Issue 1 2010Christine M. Straut Abstract Frontal analysis was carried out employing poly(ethylene-terephthalate) capillary-channeled polymer fibers as the stationary phase for the immobilization of low-molecular-weight polycyclic aromatic hydrocarbon compounds (naphthol and naphthalene) from 2% methanol/water solutions. The effects of several experimental parameters on the frontal profile, the breakthrough volume, and the equilibrium parameters were determined for each solute. The amount adsorbed at exhaustion of naphthalene and naphthol was also compared. The kinetics and thermodynamics were maintained at relatively fast flow rates/linear velocities (,6,18,mm/s). Comparisons of dynamic capacity revealed that naphthalene was more retained than naphthol, in most situations more than five times that of the naphthol adsorption. This increase in capacity is most likely due to the multilayering of naphthalene on the surface of the fibers through ,,, interactions between the solute and the fiber surface and successive layering of solute molecules. The extent of layering is a function of the flow, with faster flow rates (and subsequent shear forces) reducing the extent of adsorbate,adsorbate interactions. Although the overall loading capacity of the capillary-channeled polymer fibers is far below porous phases, there are a number of attractive attributes that support further development. [source] Enantiomeric separation of mirtazapine and its metabolites by nano-liquid chromatography with UV-absorption and mass spectrometric detectionJOURNAL OF SEPARATION SCIENCE, JSS, Issue 14 2005Salvatore Fanali Abstract Mirtazapine (MIR) and two of its main metabolites, namely, 8-hydroxymirtazapine and N -desmethylmirtazapine, were separated in totheir enantiomers by nanoLC in a laboratory-made fused-silica capillary column (75 ,m ID) packed with a vancomycin-modified silica stationary phase. The simultaneous separation of the three couples of the studied enantiomers was achieved in less than 33 min, using an experimentally optimized mobile phase delivered in the isocratic mode. Optimization of the mobile-phase composition was achieved by testing the influence of the buffer pH and concentration, the water concentration, the organic modifier type and concentration, and on the retention and resolution of the analytes. The optimum mobile-phase composition contained 500 mM ammonium acetate pH 4.5/water/MeOH/MeCN, 1 : 14 : 40 : 45 v/v/v/v. Using a UV detector at 205 nm, the method was validated studying several experimental parameters such as LOD and LOQ, intraday and interday repeatability, and linearity. Good results were achieved: LOD and LOQ were in the range 5,15 and 10,40 ,g/mL, respectively (the highest value was obtained for the DEMIR enantiomers); correlation coefficients, 0.9993,0.9999; the intraday and interday precision was acceptable (RSD < 2%) using an internal standard. The method was tested for the separation of the studied enantiomers in an extracted (solid-phase) serum sample spiked with standard racemic mixture of MIR and its two metabolites. Finally, the nanoLC system was connected to a mass spectrometer through a nanoelectrospray interface and the MS, MS2, and MS3 spectra were acquired showing the potential of the system used for characterization and identification of the separated analytes. [source] | ||||||||||