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1.
Two highly ordered isonicotinamide (INA)‐functionalized mesoporous MCM‐41 materials supporting indium and thallium (MCM‐41‐INA‐In and MCM‐41‐INA‐Tl) have been developed using a covalent grafting method. A surface functionalization method has been applied to prepare Cl‐modified mesoporous MCM‐41 material. Condensation of this Cl‐functionalized MCM‐41 with INA leads to the formation of MCM‐41‐INA. The reaction of MCM‐41‐INA with In(NO3)3 or Tl(NO3)3 leads to the formation of MCM‐41‐INA‐In and MCM‐41‐INA‐Tl catalysts. The resulting materials were characterized using various techniques. These MCM‐41‐INA‐In and MCM‐41‐INA‐Tl catalysts show excellent catalytic performance in the selective oxidation of sulfides and thiols to their corresponding sulfoxides and disulfides. Finally, it is found that the anchored indium and thallium do not leach out from the surface of the mesoporous catalysts during reaction and the catalysts can be reused for seven repeat reaction runs without considerable loss of catalytic performance. 相似文献
2.
Silver nanoparticles immobilized onto poly(4‐vinylpyridine)‐functionalized magnetic nanoparticles: A robust magnetically recyclable catalyst for oxidant‐free alcohol dehydrogenation
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A heterogeneous and recyclable catalyst with a high loading of silver nanoparticles was synthesized via the silver nanoparticles being supported onto the surface of magnetic nanoparticles coated with poly(4‐vinylpyridine). The synthesized catalyst was used in the dehydrogenation of alcohols to corresponding carbonyl compounds. A broad diversity of alcohols was converted into their corresponding carbonyl compounds in excellent yields. The catalyst was easily recovered by applying an external magnetic field and reused for seven reaction cycles without considerable loss of activity. The catalyst was fully characterized using various techniques. 相似文献
3.
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
4.
Masoomeh Jafarinejad Maryam Ezoddin Navid Lamei Khosrou Abdi Nima Babhadi‐Ashar Nazanin Pirooznia Maryam Akhgari 《Journal of separation science》2020,43(16):3266-3274
A novel effervescent tablet‐assisted demulsified dispersive liquid–liquid microextraction based on the solidification of floating organic droplet was developed to determine methadone prior to gas chromatography with flame ionization detection and gas chromatography with mass spectrometry. In this method, a tablet composed of citric acid, sodium carbonate, and 1‐undecanol was utilized. The resulting effervescent tablet generated carbon dioxide in situ to disperse 1‐undecanol in the sample. Thus, the dispersive and extraction processes were performed in one synchronous step. An aliquot of acetonitrile as the demulsifier solvent was used for the separation of two phases instead of centrifugation. Under optimal conditions, the developed method was linear up to 50 000 µg/L with correlation coefficients higher than 0.99. Moreover, limits of detection and limits of the quantification were in the range of 3‐10 and 7‐30 µg/L in water and biological samples, respectively. Intra‐ and interday precisions (n = 6) of the spiked methadone at a concentration level of 50 µg/L were over ranges of 5.1‐6.8% and 5.7‐7.1%, respectively. The preconcentration factors and recovery values were obtained in the range of 140‐145 and 98.1 to 101.6% in real samples, respectively. 相似文献
5.
Hoda Molavi Abbas Yousefpour Akbar Mirmostafa Ali Sabzi Sepideh Hamedi Milad Narimani Nazanin Abdi 《Chromatographia》2017,80(7):1129-1135
Methanol in insulating oil has been proposed as a new marker for condition assessment of the solid insulation system of power transformers. In the current work, as a first step of using the new marker, an analytical static headspace gas chromatography/mass spectrometry method has been developed, optimized, and validated to measure methanol and ethanol contents in the insulating mineral oil. The analyzing setup consists of a 6890 N gas chromatograph equipped with a 5973 network mass spectrometer (MS) in the absence of a costly headspace autosampler, and the chromatography separation was performed on a 60 m × 320 µm × 0.5 µm VF-WAXms GC column. Calibration curves have been provided using several concentrations of the alcohols, and also limit of detection (LOD), limit of quantification (LOQ), and relative standard deviation percentage (RSD%) have been determined. 相似文献
6.
M.R. Bayati Roya Molaei F. Golestani-Fard 《Colloids and surfaces. A, Physicochemical and engineering aspects》2011,373(1-3):51-60
This study sheds light on the effect of vanadium doping on hydrophilicity properties of micro arc oxidized TiO2 porous layers. Pure and V-doped titania layers, with a pore size of 50–400 nm, were grown by micro arc oxidation method. Morphology and topography of the layers were studied by SEM and AFM techniques where formation of a porous structure with a rough surface was confirmed. Moreover, phase structure and chemical composition of the samples were investigated employing XRD and XPS techniques. The pure TiO2 layers consisted of anatase and rutile phase. Vanadia phase was also detected in V-doped layers. It was also revealed that V2O5 not only dispersed in the TiO2 matrix, but also doped into the crystalline lattice. Optical properties and band gap energy of the synthesized layers were evaluated by a UV-Vis spectrophotometer. Our results showed that the band gap energy decreased when vanadium was introduced into the titania lattice. Finally, hydrophilicity of the pure and the doped layers was studied under ultraviolet and visible illuminations by measuring the water contact angle on their surface. The V-doped layers, especially those which were grown under intermediate voltages, revealed an enhanced hydrophilicity when compared to the pure TiO2 layers. 相似文献
7.
In this article the notion of repeller for multifunctions from the viewpoints of semi-bornologicul spaces is considered. The concept of lower semi-continuous multifunctions is extended by the use of semi-bornological spaces. Semi-bornological vector spaces are studied. The notion of conjugacy for semi-bornological multifunctions is considered. The persistence of repeller under conjugate relation is proved. 相似文献
8.
We demonstrate line-by-line pulse shaping of optical comb lines separated by 6.25 GHz. An array of injection-locked VCSELs independently modulate four optical comb lines at frequencies up to 3.125 GHz, updating the pulse shape on the time scale of the pulse period. 相似文献
9.
Dabre R Azad N Schwämmle A Lämmerhofer M Lindner W 《Journal of separation science》2011,34(7):761-772
Several methods for the separation of vitamins on HPLC columns were already validated in the last 20 years. However, most of the techniques focus on separating either fat- or water-soluble vitamins and only few methods are intended to separate lipophilic and hydrophilic vitamins simultaneously. A mixed-mode reversed-phase weak anion exchange (RP-WAX) stationary phase was developed in our laboratory in order to address such mixture of analytes with different chemical characteristics, which are difficult to separate on standard columns. The high versatility in usage of the RP-WAX chromatographic material allowed a baseline separation of ten vitamins within a single run, seven water-soluble and three fat-soluble, using three different chromatographic modes: some positively charged vitamins are eluted in ion exclusion and ion repulsion modes whereas the negatively charged molecules are eluted in the ion exchange mechanism. The non-charged molecules are eluted in a classical reversed-phase mode, regarding their polarities. The method was validated for the vitamin analysis in tablets, evaluating selectivity, robustness, linearity, accuracy, and precision. The validated method was finally employed for the analysis of the vitamin content of some commercially available supplement tablets. 相似文献
10.
Kris Korsak Nazanin F Dolatshad Ayona T Silva M Jill Saffrey 《Chemistry Central journal》2012,6(1):1-7