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151.
Hashem Sharghi Omid Asemani Seyed Mohammad Hossein Tabaei 《Journal of heterocyclic chemistry》2008,45(5):1293-1298
152.
Hassan Nabizadeh Bahareh Feyzi Amir Ahmad Salarian Seyed Reza Abtahi Ali Mohammadi Zahra Hami 《Electroanalysis》2023,35(1):e202200022
The development of selective and simple methods for the determination of different analytes is of great interest. This is the first time to show the applicability of graphene oxide-chitosan (GO-CS) nanocomposite for designing an electrochemical nanosensor for determination of Amlodipine, Valsartan, and Hydrochlorothiazide, simultaneously. Differential pulse voltammetrics current of AML, HCT, and VAL increased linearly in the ranges of 0.1–110, 0.1–110, and 1–230 μM with LOD of 5.5×10−2, 3.5×10−2 and 8.6×10−2 μM, respectively. Finally, GO-CS/GCE was used for the detection of these drugs in commercial tablets and compared with the reference method (HPLC). 相似文献
153.
Masoud Salavati-Niasari Seyed Nezamoddin Mirsattari Mehdi Bazarganipour 《Polyhedron》2008,27(18):3653-3661
The chemical modification of multi-wall carbon nanotubes (MWNTs) is an emerging area in material science. In the present study, an hydroxyl functionalized manganese(II) Schiff-base has been covalently anchored on modified MWNTs. The new modified MWNTs have been characterized by transmission electron microscopy (TEM), X-ray diffraction (XRD), X-ray photoelectron (XPS), thermal analysis, UV–Vis, diffuse reflectance (DRS), FT-IR spectroscopy and elemental analysis. The results suggest that the symmetrical Schiff-base; N,N-bis(4-hydroxysalicylidene)-ethylene-1,2-diamine; H2[(OH)2-salen]; is a bivalent anion with tetradentate N2O2 donors derived from the phenolic oxygens and azomethine nitrogens. The formulae was found to be [Mn((OH)2-salen)] for the 1:1 non-electrolytic complex. The multi-wall carbon nanotubes covalently anchored manganese(II) complex ([Mn((OH)2-salen)]@MWNTs) catalyze the oxidation of cyclohexene with TBHP. Oxidation of cyclohexene catalyzed by this complex gave 2-cyclohexene-1-ol, 2-cyclohexene-1-one and 1-(tert-butylperoxy)-2-cyclohexene as the major products. The manganese(II) complex covalently anchored on MWNTs shows significantly higher catalytic activity than [Mn((OH)2-salen)]. The activity of the immobilized catalyst remains nearly the same after three cycles, suggesting the true heterogeneous nature of the catalyst. This catalyst is more selective towards 2-cyclohexene-1-one. 相似文献
154.
Three diamine monomers with different derivatives of imidazole heterocyclic ring, aryl ethers and electron withdrawing trifluoromethyl groups in the backbone were synthesized and used in polycodensation reaction with various aliphatic and aromatic dicarboxylic acids for preparation of a series of novel polyamides(PAs). The PAs were obtained in high yields and possessed inherent viscosities in the range of 0.26-0.75 d L/g. All of the polymers were amorphous in nature,showed outstanding solubility and could be easily dissolved in amide-type polar aprotic solvents. They showed good thermal stability with glass transition temperatures between 162-302 ℃. Thermogravimetric analysis showed that all polymers were stable, with 10% weight loss recorded above 421 ℃ in N_2 atmospheres. All the PAs presented fluorescence upon irradiation with ultraviolet light and thus showed promise for applications in electroluminescent devices. The monomers and PAs were also screened for antibacterial activity against Gram positive and Gram negative bacteria. 相似文献
155.
Ehsan Zolfonoun Seyed Reza Yousefi 《International journal of environmental analytical chemistry》2016,96(3):203-211
In this work, multi-walled carbon nanotubes (MWCNTs)-coated cellulose acetate membrane was used for on-line extraction and pre-concentration of uranium from aqueous samples prior to inductively coupled plasma optical emission spectrometry (ICP-OES) determination. Sample solutions containing the U(VI)-2-(5-bromo-2-pyridylazo)-5-diethylaminophenol (Br-PADAP) complex were passed through the membrane. The adsorbed analyte was subsequently eluted from the membrane with acid, which was directly introduced into the ICP-OES nebuliser. The main variables affecting the pre-concentration and determination steps of uranium were studied and optimised. Under the optimised conditions, the enrichment factor of 150 and the detection limit of 0.16 μg L–1 were obtained. This method was successfully used for determination of uranium in environmental water samples. 相似文献
156.
Surface properties for three binary mixtures containing a 1-butyl-3-methylimidazolium thiocyanate ([BMIM][SCN]) and a long-chain alcohol (1-butanol, 1-pentanol and 1-hexanol) were determined by surface tension data at the following temperatures: (298.15, 308.15, 318.15, 328.15 and 338.15) K. The surface tension data over the entire mole fraction range are correlated by the Fu et al.(FLW) and Myers-Scott (MS) models. There is good agreement between the experimental data and the results of correlations for 15 binary systems (the three systems at five temperatures) with an average relative error below 1.5%. In addition, the UNIFAC group contribution method is applied for calculation of activity coefficients of components in solution. Moreover, the relative adsorptions of alcohol at the air/liquid interface are determined using Gibbs adsorption isotherm. The obtained results show that the values of adsorption for mixtures of alcohols/[BMIM][SCN] increase with increasing the alkyl chain length of alcohol and decreasing temperature. 相似文献
157.
Seyed Mehrdad Jalilian Hassan Farhadnejad Farshid Ziaee Behrouz Furughi Nia Hossein Abdollahi Vahid Najafi 《Polymer Science Series B》2016,58(6):675-680
The free radical solution polymerization of n-octyl methacrylate has been studied in benzene-d 6 in the presence of 2,2′-azobisisobutyronitrile as thermal initiator. An on-line nuclear magnetic resonance spectroscopy was applied to record the reaction data and to determine the monomer conversion at different times during the polymerization reaction. Effect of monomer and initiator concentration as well as reaction temperature on polymerization rate was studied. The order of the reaction with respect to initiator (0.45) was consistent with the classical kinetic rate equation, while the order of reaction with respect to monomer (1.87) was much greater than unity. An overall activation energy (E a = 53.8 kJ/mol) was obtained over the temperature range 328?338 K. Also, the efficiency of the synthesized poly(n-octyl methacrylate) for improving the viscosity index of the lube oil was investigated. 相似文献
158.
Elham Vatandost Fereshteh Chekin Seyed Ahmad Shahidi Yasaghi 《Russian Journal of Electrochemistry》2016,52(10):960-965
Stable silver nanoparticles were synthesized with the aid of a novel, non-toxic, eco-friendly biological material namely, green pepper extract. The aqueous pepper extract was used for reducing silver nitrate. The synthesized silver nanoparticles were analyzed with transmission electron microscopy (TEM), X-ray diffraction (XRD) and energy dispersive spectrometer (EDS). TEM image shows the formation of silver nanoparticles with average particle size of 20 nm which agrees well with the XRD data. The main advantage of using pepper extract as a stabilizing agent is that it provides long-term stability for nanoparticles by preventing particles agglomeration. To investigate the electrocatalytic efficiency of silver nanoparticles, silver nanoparticles modified carbon-paste electrode (AgNPs–CPE) displayed excellent electrochemical catalytic activities towards hydrogen peroxide (H2O2) and hydrogen evolution reaction (HER). The reduction overpotential of H2O2 was decreased significantly compared with those obtained at the bare CPE. An abrupt increase of the cathodic current for HER was observed at modified electrode. Also, the antibacterial activity of silver nanoparticle was performed using Escherichia coli and Salmonellae. The approach of plant-mediated synthesis appears to be cost efficient, eco-friendly and easy methods. 相似文献
159.
Marjaneh Jafari Fesharaki Gholamreza Nabiyouni Bita Shahdoost Seyed Farshad Akhtarianfar 《Journal of Cluster Science》2016,27(3):1005-1015
NiFe2?x Bi x O4 (x = 0, 0.1, 0.2, 0.3) nanoparticles with various grain sizes were synthesized via annealing treatment followed by ball milling of its bulk component materials. Commercially available bismuth, nickel and iron oxide powders were first mixed and then annealed at 1200 °C in an oxygen environment furnace for 4 h. The samples were then milled for 2 h by high-energy ball milling. X-ray diffraction (XRD) pattern indicated that in this stage the samples are single phase. The microstructure investigation was carried out by a scanning electron microscope with maximum magnification of 30,000. The average grain size for different samples was estimated by XRD technique and transmission electron microscopy. Magnetic behavior of the samples at room temperature was studied using an alternating gradient force magnetometry. The Néel temperature of the powders was measured by a Faraday balance. Based on magnetic studies, increase in bismuth content leads to a decrease in the saturation magnetization, coercive field and Néel temperature. This can be attributed to the substitution of Bi3+ ion in the ferrite system as a nonmagnetic cation. 相似文献
160.
Mojtahedi MM Chalavi S Ghassempour A Tabar-Heydar K Sharif SJ Malekzadeh M Aboul-Enein HY 《Biomedical chromatography : BMC》2007,21(3):234-240
This work aims to evaluate for the enantiomeric separations of three agrochemical toxins: haloxyfop-methyl, fenoxaprop-p-ethyl and indoxacarb on crystalline degradation products-chiral stationary phase (CDP-CSP) of high-performance liquid chromatography (HPLC) under normal and polar organic phases. In the normal phase, the mobile phase was n-hexane with alcohols including methanol and isopropanol as polar modifiers. In the polar organic phase mode, the mobile phase was methanol with different percentages of triethylammunium acetate. The influence of flow rate (0.3-0.9 mL/min), analyte concentration and silica gel particle sizes (10, 15 and 30 microm) was investigated. This new chiral stationary phase showed excellent stereoselectivity for the two enantiomers of haloxyfop-methyl and fenoxaprop-p-ethyl and chiral recognition for indoxacarb under normal-phase mode. However, under polar organic phase, only indoxacarb was separated (alpha < 1.5). The chromatographic results were compared with commercial chiral columns. 相似文献