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101.
Saeed Dehghanpour Rhett Kempe Sreenivas Balireddi Lida Fotouhi Farzaneh Tabasia Fresia Mojahed Samaneh Salek 《无机化学与普通化学杂志》2006,632(14):2321-2325
A novel ligand, N,N′‐Bis‐[3‐(2‐nitrophenyl)‐allylidene]‐ethane‐1,2‐diamine (nca2en), and their corresponding copper(I) complexes, [Cu(ncaen)2]ClO4 ( 1 ), and [Cu(nca2en)(PPh3)2]BPh4 ( 2 ), have been synthesized and characterized by CHN analyses, 1H and 13C‐NMR, IR, and UV‐Vis spectroscopy. The crystal and molecular structures of [Cu(ncaen)2]ClO4 ( 1 ), and [Cu(nca2en)(PPh3)2]BPh4 ( 2 ), were determined by X‐ray crystallography from single‐crystal data. The coordination polyhedron about the copper(I) atom in the two complexes is best described as a distorted tetrahedron. A quasireversible redox behavior is observed for complex 1 and 2 (E1/2 = 0.55 and 0.95 V, respectively). 相似文献
102.
Wetting characteristics of micro-nanorough substrates of aluminum and smooth silicon substrates have been studied and compared by depositing hydrocarbon and fluorinated-hydrocarbon coatings via plasma enhanced chemical vapor deposition (PECVD) technique using a mixture of Ar, CH4 and C2F6 gases. The water contact angles on the hydrocarbon and fluorinated-hydrocarbon coatings deposited on silicon substrates were found to be 72° and 105°, respectively. However, the micro-nanorough aluminum substrates demonstrated superhydrophobic properties upon coatings with fluorinated-hydrocarbon providing a water contact angle of ∼165° and contact angle hysteresis below 2° with water drops rolling off from those surfaces while the same substrates showed contact angle of 135° with water drops sticking on those surfaces. The superhydrophobic properties is due to the high fluorine content in the fluorinated-hydrocarbon coatings of ∼36 at.%, as investigated by X-ray photoelectron spectroscopy (XPS), by lowering the surface energy of the micro-nanorough aluminum substrates. 相似文献
103.
104.
Farzaneh Ebrahimgol Hossein Tavanai Farzaneh Alihosseini Taghi Khayamian 《先进技术聚合物》2014,25(9):1001-1007
This work reports on producing wool keratin nanoparticles through electrospraying. Wool keratin is a natural biodegradable and biocompatible protein. Keratin powder has found application in hygiene, cosmetics, filtration, tissue engineering scaffolds, and controlled drug release. Like other nano materials, the performance of keratin in submicron size range changes drastically. Electrospraying is a technique that is capable of producing nanosized, regular, and spherical particles. To prepare the electrospraying wool keratin solution, keratin was recovered from descaled wool fibers by dissolving it in mercaptoethanol first, and keratin sponge was obtained. Then, the keratin sponge was dissolved in formic acid that provided the electrospraying solution. This research involved primarily an investigation on the effect of important electrospraying conditions such as polymer concentration, feed rate, voltage, and nozzle‐collector distance on the average particle size of the electrosprayed nanoparticles. The results showed that the proper concentration of keratin in formic acid for the electrospraying keratin nanoparticle was about 0.5% (w/v). As far as electrospraying conditions are concerned, decreasing feed rate and increasing nozzle‐collector distance led to lower average particle size. Voltage did not show a practically significant effect on the average particle size. The average size of the electrosprayed keratin nanoparticles fabricated in this work lies in the range of 36–72 nm. Fourier transform infrared Fourier transform infrared (FTIR) spectra showed that electrosprayed keratin nanoparticles contain –SO2–S– and –SO–S– linkages. Copyright © 2014 John Wiley & Sons, Ltd. 相似文献
105.
106.
VOSO4 immobilized within nanoreactors of Al-MCM-41 (VO2+/Al-MCM-41) was synthesized and characterized by X-ray diffraction, Fourier transform infrared spectroscopy, nitrogen adsorption-desorption, and chemical analysis techniques. The prepared VO2+/Al-MCM-41 successfully catalyzes the oxidation of aryl alkyl sulfides and up to 99% conversion and 90% selectivity for the corresponding sulfoxides were obtained with H2O2 as oxidant in acetonitrile at room temperature in 30 min. 相似文献
107.
108.
A new approach, employing cloud point extraction (CPE) in combination with thermal lens spectrometry (TLS), has been developed for the determination of cobalt. The CPE and TLS methods have good matching conditions for combination because TLS is suitable for low volume samples obtained after CPE and for organic solvents, which are used for dissolving the remaining analyte phase.1-(2-Pyridylazo)-2-naphthol (PAN) was used as a complexing agent and octylphenoxypolyethoxyethanol (Triton X-114) was added as a surfactant; then the pH of solution was adjusted. After phase separation at 50 °C based on the cloud point extraction of the mixture, the surfactant-rich phase was dried and the remaining phase was dissolved using 20 μL of carbon tetrachloride. The obtained solution was introduced into the quartz micro cell and the analyte was determined by thermal lens spectrometry. The He-Ne laser (632.8 nm) was used as both the probe and the excite source.Under optimum conditions, the analytical curve was linear for the concentration range of 0.2-40 ng mL−1 and the detection limit was 0.03 ng mL−1. The enhancement factor of 470 was achieved for a 10 mL sample. Relative standard deviations were lower than 5%.The method was successfully applied to the extraction and determination of cobalt in tap, river and sea water. 相似文献
109.
Jamali MR Assadi Y Shemirani F Hosseini MR Kozani RR Masteri-Farahani M Salavati-Niasari M 《Analytica chimica acta》2006,579(1):68-73
A new functionalized mesoporous silica (MCM-41) using salicylaldehyde was utilized for the separation, preconcentration and determination of uranium in natural water by inductively coupled plasma atomic emission spectrometry (ICP-AES).Experimental conditions for effective adsorption of trace levels of U(VI) were optimized. The preconcentration factor was 100 (1.0 mL of elution for a 100 mL sample volume). The analytical curve was linear in the range 2-1000 μg L−1 and the detection limit was 0.5 ng mL−1. The relative standard deviation (R.S.D.) under optimum conditions was 2.5% (n = 10). Common coexisting ions did not interfere with the separation and determination of uranium at pH 5. The sorbent exhibited excellent stability and its sorption capacity under optimum conditions has been found to be 10 mg of uranium per gram of sorbent. The method was applied for the recovery and determination of uranium in different water samples. 相似文献
110.
A computational technique based on the Müntz polynomials and meshless method has been presented for the solution of nonlinear and linear space fractional partial differential equations (PDEs). The meshless method that is used in this study is the new version of backward substitution method (BSM). First, the time-derivative term is discretized by the Crank-Nicolson method. Then, the approximate solution is given as the separation of the approximation of the boundary data and the correcting functions using the Müntz polynomials. In general form, this approximate solution that does not necessarily satisfy the original equation is shown as the sum of the system basics in which it consists free parameters. Finally, these parameters are determined by the BSM method inside the domain. The main advantage of the method is efficiency and reliability that is examined by six numerical experiments. 相似文献