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51.
Dr. Tran Quang Hung Dr. Ferial Terki Dr. Souleymane Kamara Mourad Dehbaoui Prof. Salam Charar Brajalal Sinha Prof. CheolGi Kim Dr. Philippe Gandit Il'ya A. Gural'skiy Dr. Gabor Molnar Dr. Lionel Salmon Dr. Helena J. Shepherd Dr. Azzedine Bousseksou 《Angewandte Chemie (International ed. in English)》2013,52(4):1058-1058
52.
Georgina M. S. Alves Júlia M. C. S. Magalhães Helena M. V. M. Soares 《Electroanalysis》2013,25(5):1247-1255
A simple, fast, sensitive and greener voltammetric procedure for simultaneous analysis of nickel (Ni) and cobalt (Co) by square wave adsorptive cathodic stripping voltammetry (SW‐AdCSV) using a solid bismuth vibrating electrode is presented for the first time. The procedure enables to determine Ni together with Co, in ammonia buffer 0.1 M (pH 9.2) and in the presence of oxygen, and involves an adsorptive accumulation of metal‐dimethylglyoxime (Ni‐DMG and Co‐DMG) complexes on the electrode surface. For Ni and Co, the detection limits, obtained with 30 s of accumulation time, were 0.6 and 1.0 µg L?1, respectively. The method was free of metals (Cd2+, Cr3+, Cr6+, Cu2+, Fe3+ and Pb2+ up to 50 µg L?1, Al3+ and Mn2+ up to 500 µg L?1; Zn2+ up to 300 µg L?1) interferences up to the concentrations mentioned in brackets. The proposed method was validated for simultaneous determination of Ni and Co in a certified reference surface and river waters with good results. 相似文献
53.
Georgina M. S. Alves Júlia M. C. S. Magalhães Roma Tauler Helena M. V. M. Soares 《Electroanalysis》2013,25(8):1895-1906
Simultaneous anodic stripping voltammetric determination of Pb and Cd is restricted on gold electrodes as a result of the overlapping of these two peaks. This work describes the quantitative determination of a binary mixture system of Pb and Cd, at low concentration levels (up to 15.0 and 10.0 µg L?1 for Pb and Cd, respectively) by differential pulse anodic stripping voltammetry (DPASV; deposition time of 30 s), using a green electrode (vibrating gold microwire electrode) without purging in a chloride medium (0.5 M NaCl) under moderate acidic conditions (HCl 1.0 mM), assisted by chemometric tools. The application of multivariate curve resolution alternating least squares (MCR‐ALS) for the resolution and quantification of both metals is shown. The optimized MCR‐ALS models showed good prediction ability with concentration prediction errors of 12.4 and 11.4 % for Pb and Cd, respectively. The quantitative results obtained by MCR‐ALS were compared to those obtained with partial least squares (PLS) and classical least squares (CLS) regression methods. For both metals, PLS and MCR‐ALS results are comparable and superior to CLS. For Cd, as a result of the peak shift problem, the application of CLS was unsuitable. MCR‐ALS provides additional advantage compared to PLS since it estimates the pure response of the analytes signal. Finally, the built up multivariate calibration models, based either in MCR‐ALS or PLS regression, allowed to quantify concentrations of Pb and Cd in surface river water samples, with satisfactory results. 相似文献
54.
Tomáš Křížek Veronika Doubnerová Helena Ryšlavá Pavel Coufal Zuzana Bosáková 《Analytical and bioanalytical chemistry》2013,405(8):2425-2434
Enzyme assays of β-N-acetylhexosaminidase from Aspergillus oryzae using capillary electrophoresis in the offline and online setup have been developed. The pH value and concentration of the borate-based background electrolyte were optimized in order to achieve baseline separation of N,N′,N″-triacetylchitotriose, N,N′-diacetylchitobiose, and N-acetyl-d-glucosamine. The optimized method using 25 mM tetraborate buffer, pH 10.0, was evaluated in terms of repeatability, limits of detection, quantification, and linearity. The method was successfully applied to the offline enzyme assay of β-N-acetylhexosaminidase, which was demonstrated by monitoring the hydrolysis of N,N′,N″-triacetylchitotriose. The presented method was also utilized to study the pH dependence of enzyme activity. An online assay with N,N′-diacetylchitobiose as a substrate was developed using the Transverse Diffusion of Laminar Flow Profiles model to optimize the injection sequence and in-capillary mixing of substrate and enzyme plugs. The experimental results were in good agreement with predictions of the model. The online assay was successfully used to observe the inhibition effect of N,N′-dimethylformamide on the activity of β-N-acetylhexosaminidase with nanoliter volumes of reagents used per run and a high degree of automation. After adjustment of background electrolyte pH, an online assay with N,N′,N″-triacetylchitotriose as a substrate was also performed. Figure
Electropherograms resulting from online enzyme assays of β-N-acetylhexosaminidase for chitobiose as a substrate with 10-min (red line), 5-min (blue line) and 0-min (black line) reaction time. Peak identification: 1 chitobiose, 2 N-acetylglucosamine 相似文献
55.
Abstract A power law behaviour of dielectric loss versus frequency has been found in members of the 4,4′-di-n-alkyloxyazoxybenzene series. For each member the scaling of the data with respect to v/v max is possible in the liquid-crystalline temperature range; this suggests a fractal-like geometry in nematic and smectic phases. The values of the scaling exponents, indicating a cooperativity of molecular reorientation around the short axes, exhibit an odd–even effect. 相似文献
56.
Abstract The phase diagram of a two component system composed of two smectic compounds: 4-octyloxy-4′-cyanobiphenyl (8OCB) and 4-isothiocyanatophenyl 4-butylbenzoate (4TPB) was investigated. Three Miesowicz viscosity coefficients η1, η2, η3 and the refractive indices at different temperatures as well as the enthalpies of the phase transitions were measured. It was stated, that the properties of the induced nematic phase, for example, the nematic phase existing between two smectic regions, are the same as the ones observed in the case of low viscosity nematic mesogens. 相似文献
57.
Abstract This paper presents a new analysis of all (old and new) quasi-elastic neutron scattering results obtained for seven members of the PAA series (n = 1,…, 7). The analysis is based upon a discussion of the parameter p, which is the deviation of the intensity of the elastic component from the intensity demanded by a reorientational model. If the value of this parameter is negative, it may be interpreted as an indication of an additional motion which has not been taken into account in the model. The first model analysed in this way for all seven substances in the nematic phase was that of the rotational diffusion of the whole molecule in its stretched (trans) conformation, around the long axis. A very large negative values of p (p ? -60 per cent) was obtained, clearly showing that some motions have been neglected. The second model was that of the rotational diffusion of moieties consisting of benzene rings plus alkoxy side-chains. The diffusion occurs around the benzene para-axes, and the alkoxy side-chains are assumed to be in their trans conformations. Less negative values of p (p ? -10 per cent) were obtained, indicating that other motions still exist. Since these must take place in the alkyl chains, we make a third step in the analysis, in which we retain the second model but now take substances which are alkyl-deuterated (which means masking for the neutron incoherent scattering method). Now values of p which are nearly zero are obtained which means that the motions previously ignored indeed exist in the alkyl chains. An even-odd effect observed in the dependence of p on n indicates that even molecules are more mobile than odd ones, probably due to less steric hindrance in more ordered, even substances. A critical discussion on reorientational correlation times is also presented. 相似文献
58.
Stanislaw Urban Krzysztof Czuprynski Roman Dąbrowski Bo Gestblom Joanna Janik Horst Kresse 《Liquid crystals》2013,40(5):691-696
Results of the dielectric studies of nine members of the nBT (4-n-alkyl-4'-thiocyanatobiphenyl, n= 2-10) homologous series in the crystal E (E) and isotropic (I) phases are presented. The dependence of the static permittivity ?s in the isotropic phase, the longitudinal relaxation times τis and τ∥, and the activation enthalpies ΔH is and ΔH ∥ on the number of carbon atoms in the alkyl chain n are analysed. A considerable increase in the retardation factor g= τ∥/τis with decreasing n is observed. The results are compared with those obtained for similar two-ring homologous series. The parameters characterizing the molecular rotations around the short axis in the E phase (τ∥ and ΔH ∥) indicate a hardening of this solid-like phase with shortening of the alkyl chain. 相似文献
59.
Gunilla Niklasson Ingemar Kvarnström Björn Classon Bertil Samuelsson† Ulrika Nillroth Helena Danielson 《Journal of carbohydrate chemistry》2013,32(5):555-569
ABSTRACT D-Mannitol was used as precursor for the synthesis of acyclic C 2 symmetric potential HIV-1 protease inhibitors. The 1- and 6-hydroxy groups of D-mannitol were substituted by -NHBoc, -NHValZ, -SAr, -SOAr and -SO2Ar and the 2-and 5-hydroxy groups were benzylated. In some products one of the central hydroxyl groups was either inverted or deoxygenated. Despite a close structural similarity to previously published inhibitors none of the products showed significant inhibitory activity against HIV-1 protease. 相似文献
60.
In this study the effect of the mercerization degree on the water retention value (WRV) and tensile properties of compression molded sulphite dissolving pulp was evaluated. The pulp was treated with 9, 10, or 11 % aqueous NaOH solution for 1 h before compression molding. To study the time dependence of mercerization the pulp was treated with 12 wt% aqueous NaOH for 1, 6 or 48 h. The cellulose I and II contents of the biocomposites were determined by solid state cross polarization/magic angle spinning carbon 13 nuclear magnetic resonance (CP/MAS 13C NMR) spectroscopy. By spectral fitting of the C6 and C1 region the cellulose I and II content, respectively, could be determined. Mercerization decreased the total crystallinity (sum of cellulose I and cellulose II content) and it was not possible to convert all cellulose I to cellulose II in the NaOH range investigated. Neither increased the conversion significantly with 12 wt% NaOH at longer treatment times. The slowdown of the cellulose I conversion was suggested as being the result from the formation of cellulose II as a consequence of coalescence of anti-parallel surfaces of neighboring fibrils (Blackwell et al. in Tappi 61:71–72, 1978; Revol and Goring in J Appl Polym Sci 26:1275–1282, 1981; Okano and Sarko in J Appl Polym Sci 30:325–332, 1985). Compression molding of the partially mercerized dissolving pulps yielded biocomposites with tensile properties that could be correlated to the decrease in cellulose I content in the pulps. Mercerization introduces cellulose II and disordered cellulose and lowered the total crystallinity reflected as higher water sensitivity (higher WRV values) and poorer stiffness of the mercerized biocomposites. 相似文献