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Moutab Sahihazar Milad Ahmadi Mohammad Taghi Nouri Mina Rahmani Meisam 《Journal of Solid State Electrochemistry》2019,23(6):1641-1650
Journal of Solid State Electrochemistry - Nanostructured carbon material (NSCM) based chemiresistive sensors are popular for sensing different analytes because of their high sensitivity, low cost,... 相似文献
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Zheng Yuanzhou Zhang Xinzhu Soleimani Mobareke Mohammad Taghi Hekmatifar Maboud Karimipour Arash Sabetvand Roozbeh 《Journal of Thermal Analysis and Calorimetry》2021,144(6):2515-2523
Journal of Thermal Analysis and Calorimetry - It is interesting to investigate the number of nanoparticle (NP) and temperature effects on H2O/CuO nanofluid thermal conductivity and the atomic... 相似文献
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Molecular Diversity - 5-Amino-pyrazoles have proven to be a class of fascinating and privileged organic tools for the construction of diverse heterocyclic or fused heterocyclic scaffolds. This... 相似文献
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Bahram Mokhtari Kobra Pourabdollah Naser Dallali 《Journal of Radioanalytical and Nuclear Chemistry》2011,287(3):921-934
Calixarenes has been subject to extensive research in development of many extractants, transporters, stationary phases, electrode ionophores and optical and electrochemical sensors over the past four decades. In this paper, the nuclear applications of calixarenes are summarized in six fields including complexation studies, solvent extraction, membrane transport, chromatography, luminescent and colorimetric applications, and electroanalytical applications. In the first to fourth sections, the extractability, extraction equilibria and extraction constants of lanthanide, actinide and other nuclear waste cations ions, which were subjected to solvent extraction by the macrocyclic ligands, are reviewed. In two last sections, the analytical applications of calixarene complexes towards nuclear waste cations, including spectroscopic and electroanalytic sensors, are discussed. The examples described in this review illustrate the potential of calixarene derivatives in the rapidly growing field of cations recognition in nuclear wastes. 相似文献
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Mohammad Taghi Taghizadeh Nazanin Yeganeh Mostafa Rezaei 《Journal of Thermal Analysis and Calorimetry》2014,118(3):1733-1746
A peak deconvolution procedure used for the analysis of data corresponding to simultaneous overlapping processes begins with separation of individual processes using functions such as Gaussian, Lorentzian, Weibull, and Fraser–Suzuki (FS) followed by application of kinetic analysis methods to the separated peaks. We propose a coupled peak deconvolution procedure to link the parameters of the FS functions of similar peaks in two DTG curves obtained at different linear heating rates, so that the coordinates of each peak can be obtained in a constrained manner. The proposed technique is a kinetic deconvolution method rather than a pure mathematical deconvolution technique. To analyze individual peaks in our study, the non-parametric kinetic and Freidman’s isoconversional methods have been applied to determine kinetic triplet of each process. This technique has been tested with both simulated and experimental data. Using this technique, the effects of molecular weight and degree of hydrolysis of polyvinyl alcohol (PVA) samples on reaction mechanism and activation energy of thermal degradation were studied. The presence of acetate group in the PVA samples causes thermal stability, decreases the rate of main reactions, and increases the activation energy. The results of this study may help tailor heat-resistant materials with proper choice of polymer characteristics. 相似文献
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Mohammad Saraji Taghi Khayamian Zahra Hashemian 《Journal of separation science》2014,37(23):3518-3525
In this work, a polypyrrole/multiwalled carbon nanotubes composite decorated with Fe3O4 nanoparticles was chemically synthesized and applied as a novel adsorbent for the extraction of methocarbamol from human plasma. Electrospray ionization ion mobility spectrometry was used for the determination of the analyte. The properties of the magnetic‐modified adsorbent were characterized by scanning electron microscopy, transmission electron microscopy, Fourier transform IR spectroscopy, and X‐ray diffraction. The effects of experimental parameters on the extraction efficiency of the sorbent were investigated. Under the optimized conditions, the linear dynamic range was found to be 2–150 ng/mL with the detection limit of 0.9 ng/mL. The relative standard deviation was 5.3% for three replicate measurements of methocarbamol in plasma sample. The extraction efficiency of the sorbent for the determination of different drugs with various polarities was also compared to that of Fe3O4‐polypyrrole and Fe3O4‐multiwalled carbon nanotubes sorbents. Finally, the method was used for the determination of methocarbamol in blood samples. 相似文献
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M.C. Menet C.H. Cottart M. Taghi V. Nivet-Antoine D. Dargère F. Vibert O. Laprévote J.-L. Beaudeux 《Analytica chimica acta》2013
Resveratrol is a polyphenol that has numerous interesting biological properties, but, per os, it is quickly metabolized. Some of its metabolites are more concentrated than resveratrol, may have greater biological activities, and may act as a kind of store for resveratrol. Thus, to understand the biological impact of resveratrol on a physiological system, it is crucial to simultaneously analyze resveratrol and its metabolites in plasma. This study presents an analytical method based on UHPLC-Q-TOF mass spectrometry for the quantification of resveratrol and of its most common hydrophilic metabolites. The use of 13C- and D-labeled standards specific to each molecule led to a linear calibration curve on a larger concentration range than described previously. The use of high resolution mass spectrometry in the full scan mode enabled simultaneous identification and quantification of some hydrophilic metabolites not previously described in mice. In addition, UHPLC separation, allowing run times lower than 10 min, can be used in studies that requiring analysis of many samples. 相似文献
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Seyed Abolghasem Kahani Mohammad Sabeti Mohammad Taghi Yosefi 《Phosphorus, sulfur, and silicon and the related elements》2013,188(11):1584-1590
Abstract The oxidation of thiocyanate to polythiocyanic acid by peroxydisulfate was carried out in an aqueous solution at room temperature. The primary step is the decomposition of peroxydisulfate into sulfate-free radicals. At room temperature in the presence of peroxydisulfate as a oxidizing agent, HSCN polymerizes to (HSCN)n. The oxidation of thiocyanate in an aqueous solution is often complicated, but here we obtained the polythiocyanic acid as a major product. The products were characterized by elemental analysis, IR, UV- visible, H-NMR spectroscopy, and X-ray powder diffraction. 相似文献