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G. F. Prozorova I. V. Mazyar V. V. Nosyreva S. A. Korzhova T. I. Vakul’skaya B. A. Trofimov 《Russian Journal of General Chemistry》2014,84(5):892-900
Interaction of trichloroethene with sodium tetra- and pentasulfide (prepared in turn from sodium sulfide and elemental sulfur) has lead to new family of polyvinylenepolysulfides containing up to 94% of sulfur. The polymers were found highly electrochemically active when applied as active cathode for lithium batteries. 相似文献
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G. F. Prozorova I. V. Mazyar S. A. Korzhova T. G. Ermakova N. P. Kuznetsova M. V. Trenikhin Yu. G. Kryazhev B. A. Trofimov 《Doklady Chemistry》2017,473(1):53-56
New sulfur-containing copolymers based on poly(vinyl chloride) have been prepared by the nucleophilic substitution of chlorine atoms by sulfur atoms using sodium tetra- and pentasulfides. It has been shown that these copolymers can be carbonized to produce sulfur-containing carbon materials with residual chlorine content about 2 wt %. 相似文献
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The present study reports the development, validation and application of a new green liquid chromatographic method for the determination of glutathione (GSH) in vegetable samples. In this work we introduce—for the first time—ethyl propiolate (EP) as an advantageous post-column derivatization reagent for thiolic compounds. GSH (tR = 6.60 min) and N-acetylcysteine (NAC, internal standard) (tR = 11.80 min) were separated efficiently from matrix endogenous compounds by using a 100% aqueous mobile phase (0.1%, v/v CH3COOH in 1 mmol L−1 EDTA, QV = 0.5 mL min−1) and a Prevail® reversed phase column that offers the advantage of stable packing material in aqueous mobile phases. The parameters of the post-column reaction (pH, amount concentration of the reagent, flow rates, length of the reaction coil and temperature) were studied. The linear determination range for GSH was 1–200 μmol L−1 and the LOD was 0.1 μmol L−1 (S/N = 3). Total endogenous GSH was determined in broccoli, potato, asparagus and Brussels sprouts using the standards addition approach. The accuracy was evaluated by both recovery experiments (R = 91–110%) and comparison to an o-phthalaldehyde/glycine corroborative post-column derivatization fluorimetric method. 相似文献
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Zarrin Es’haghi Zohreh Rezaeifar Gholam-Hossein Rounaghi Zahra Alian Nezhadi Mazyar Ahmadi Golsefidi 《Analytica chimica acta》2011,(1):8313
A novel solid-phase microextraction technique using a hollow fiber-supported sol–gel combined with multi-walled carbon nanotubes was employed in the determination of phenobarbital in wastewater. In this new technique, a silica-based, organic–inorganic polymer containing functionalized multi-walled carbon nanotubes (MWCNTs) was prepared with sol–gel technology via the reaction of tetraethylorthosilicate (TEOS) with an acidic catalyst (HCl). This sol was injected into a polypropylene hollow fiber segment for in situ gelation. This device operated in direct immersion sampling mode. The experimental setup is simple and affordable, and the device is disposable, so there is no risk of cross-contamination or carry-over. Parameters affecting extraction such as pH of the aqueous solution, ageing and extraction times, aqueous sample volume, agitation speed and carbon nanotube amount were optimized. Linearity was observed over a range of 0.50–5000 ng mL−1, with an estimation coefficient (r2) higher than 0.982. The limit of detection (LOD) was 0.32 ng mL−1 (n = 5), and repeatability (RSD% = 2.9) was from the average of three levels of analyte concentrations (1, 1000 and 4500 ng mL−1) with three replicates for each within a single day. Finally, a pre-concentration factor of 2100 was obtained for phenobarbital. 相似文献
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Jayasundera S Burleigh MC Zeinali M Spector MS Miller JB Yan W Dai S Markowitz MA 《The journal of physical chemistry. B》2005,109(19):9198-9201
Benzene, diethylbenzene, and ethylenediamine-bridged bistrialkoxy precursors were used in the synthesis of multifunctional PMO copolymers for the adsorption of phenols and metal ions. Polyoxyethylene(10) stearyl ether (Brij 76) was used as the structure director with the surfactant template approach in the synthesis. The resulting PMO copolymers with two or more bridging groups have been characterized by nitrogen gas adsorption, powder X-ray diffraction, and 13C and 29Si solid-state NMR. These organosilicas exhibit large surface areas, narrow pore size distributions, large total pore volumes, and pore ordering consistent with well ordered, hexagonally packed p6mm structures. Minimal competitive effects were observed on the adsorption of p-chlorophenol to the copolymers in the presence of copper ions in solution. Similarly, the presence of p-chlorophenol in solution or adsorbed onto the copolymers did not interfere with copper adsorption. Replacement of a small portion of the benzene bridge in the 90:10 BENZ:EDA copolymer with diethylbenzene produced a copolymer 2.5-fold more efficient for p-chlorophenol adsorption. ICP analysis revealed that greater than 98% of adsorbed copper was removed during extraction with HCl, and this extraction process can be repeated with no difference in copper adsorption after regeneration. 相似文献
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Mazyar N. L. Annenkov V. V. Kruglova V. A. Anan'ev S. M. Danilovtseva E. N. Rokhin A. V. Zinchenko S. V. 《Russian Chemical Bulletin》2000,49(12):2013-2017
The interaction of poly(1-vinylimidazole) and poly(1-vinyl-1,2,4-triazole) with HCl and alkalies in aqueous and water-salt solutions was investigated by potentiometric titration, viscosimetry, 1H and 13C NMR, and UV spectroscopy. The effect of the nature and concentration of low-molecular counterions was found. The interaction of poly(1-vinylazoles) with the acid results in the protonation of the azole cycle. The interaction of poly(1-vinylazoles) with alkalies is stipulated by the capability of the pyridine N atom of forming a coordination bond with the metal ion and that of the unsaturated pi-system of the heterocycle of coordinating with the anions. 相似文献
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Threshold photoelectron-photoion coincidence (TPEPICO) spectroscopy has been used to investigate the unimolecular chemistry of gas-phase methyl 2-methyl butanoate ions [CH3CH2CH(CH3)COOCH3·+]. This ester ion isomerizes to a lower energy distonic ion [CH2CH2CH(CH3)COHOCH3·+] prior to dissociating by the loss of C2H4. The asymmetric time of flight distributions, which arise from the slow rate of dissociation at low ion energies, provide information about the ion dissociation rates. By modeling these rates with assumed k(E) functions, the thermal energy distribution for room temperature sample, and the analyzer function for threshold electrons, it was possible to extract the dissociative photoionization threshold for methyl 2-methyl butanoate which at 0 K is 9.80 ± 0.01 eV as well as the dissociation barrier of the distonic ion of 0.86 ± 0.01 eV. By combining these with an estimated heat of formation of methyl 2-methyl butanoate, we derive a 0 K heat of formation of the distonic ion CH2CH2CH(CH3)COHOCH3·+ of 101.0 ± 2.0 kcal/mol. The product ion is the enol of methyl propionate, CH3CHCOHOCH3·+, which has a derived heat of formation at 0 K of 106.0 ± 2.0 kcal/mol. 相似文献