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171.
Data for the adsorption of CO2 on 5A (CaA) and 13X (NaX) zeolite are critically evaluated. In addition, fresh data for the adsorption of CO2 on 13X zeolite is reported. Three intrinsic properties are examined: q max , the saturation loading, K H , the Henry constant, and (?ΔH) q , the isosteric heat of sorption. Below a reduced temperature T r , of 0.9, the q max values for both 5A and 13X zeolites are similar to theoretical values that may be derived using zeolitic crystallographic properties and the sorbate density calculated using the Rackett equation. For the region 0.9 ≤ Tr ≤ 1.0, the calculated q max values exceed the theoretical values similarly calculated, indicating that the molecules have a smaller molar volume than in a similar liquid phase. This is a similar result to that observed in ionic liquids. Linear regressed equations are derived for q max for the region 0.9 ≤ Tr ≤ 1.25. The Henry constant values for 5A are remarkably consistent for the five studies examined, with a correlation coefficient, R, of 0.999 for the van’t Hoff equation, but for the seven studies examined in 13X the data is more disperse as indicated by a correlation coefficient R of 0.899 for the van’t Hoff equation. The values of (?ΔH) q , the isosteric heat of sorption are in agreement with the literature. An explanation is advanced for the discrepancy between the higher heats of sorption values obtained calorimetrically from those obtained from isosteric adsorption studies. Finally, the fresh data is observed to fit the Toth model with regression coefficients of 0.999. However, the parameters obtained for the Toth equation by regression are significantly different from the intrinsic properties derived earlier, indicating the difficulty of deriving intrinsic parameters from isotherm fits. 相似文献
172.
Hassan A. Zedan M. Alghamdi Seham Sh. Tantawy 《Mathematical Methods in the Applied Sciences》2015,38(17):4357-4364
We study in this paper the Q‐symmetry and conditional Q‐symmetries of Drinfel'd–Sokolov–Wilson equations. The solutions which we obtain in this paper take the form of convergent power series with easily computable components. Copyright © 2014 John Wiley & Sons, Ltd. 相似文献
173.
Electroless Ni–P and Ni–P–TiCN composite coatings have been deposited successfully on Al substrates. Scanning electron microscopy (SEM) and energy dispersive X‐ray (EDX) techniques were applied to study the surface morphology and the chemical composition of the deposited films. Moreover, X‐ray diffraction (XRD) proved that Ni–P and Ni–P–TiCN deposits have amorphous structures. The properties of Ni–P–TiCN/Al composite films such as hardness, corrosion resistance and electrocatalytic activity were examined and compared with that of Ni–P/Al film. The results of hardness measurements reveal that the presence of TiCN particles with Ni–P matrix improves its hardness. Additionally, the performance against corrosion was examined using Tafel lines and electrochemical impedance spectroscopy techniques in both of 0.6 M NaCl and a mixture of 0.5 M H2SO4 with 2 ppm HF solutions. The results indicate that the incorporation of high dispersed TiCN particles into Ni–P matrix led to a positive shift of the corrosion potential and an increase in the corrosion resistance for all aluminum substrates after their coating with Ni–P–TiCN. In addition, Ni–P–TiCN/Al electrodes showed a higher electrochemical catalytic activity and stability toward methanol oxidation in 0.5 M NaOH solution compared with that of Ni–P/Al. Copyright © 2014 John Wiley & Sons, Ltd. 相似文献
174.
Atsutoshi Yamada Yuki Watanabe Kyoko Noda Sumitaka Itoh Koji Ishihara Masahiko Inamo Refat Moustafa Hassan Hideo D. Takagi 《Journal of solution chemistry》2014,43(9-10):1479-1486
The reduction reaction of the Cu(II)–pitn complex (pitn = 1,3-di(pyridine-2-carboxaldimino)propane) by decamethylferrocene [Fe(Cp*)2] was examined in acetonitrile. The observed pseudo-first-order rate constants exhibited saturation kinetics with increasing excess amount of [Fe(Cp*)2]. Detailed analyses revealed that the reaction is controlled by a structural change prior to the electron transfer step, rather than a conventional bimolecular electron transfer process preceded by ion pair (encounter complex) formation. The rate constant for the structural change was estimated to be 275 ± 13 s?1 at 298 K (?H* = 33.3 ± 1.0 kJ·mol?1, ?S* = 86 ± 5 J·mol?1·K?1), which is the fastest among gated reactions involving CuN4 complexes. It was confirmed by EPR measurement and Conflex calculations that the dihedral angle between the two N–N planes is significantly large (40°) in solution whereas it is merely 17.14° in the crystal. 相似文献
175.
Anik Goswami Gunjan Verma P. A. Hassan Vinod K. Aswal 《Journal of Dispersion Science and Technology》2014,35(12):1717-1726
The adsorption behavior of binary mixtures comprising nonionic surfactants at the air–water interface has been studied by bubble pressure tensiometry at concentrations above and below their critical micelle concentrations. Surfactants with the same hydrocarbon chains but different degree of ethoxylations were chosen as the components to understand their mixing behavior at equilibrium and dynamic conditions. At short times, the adsorption is found to be diffusion limited for individual components as well as for the mixtures, as predicted by the Ward and Tordai model. The effective diffusion coefficient of the monomers in the mixed state displays a dynamic synergism, consistent with the molecular thermodynamic model for dynamic surface tension. However, the equilibrium surface tension and micellar diffusion coefficient of the mixtures exhibit ideal behavior. 相似文献
176.
K. F. Hassan S. Spellerberg B. Scholten Z. A. Saleh S. M. Qaim 《Journal of Radioanalytical and Nuclear Chemistry》2014,302(1):689-694
A novel anion-exchange chromatographic method for separation of radioiodine from an antimony target irradiated with 3He- or α-particles was developed, with separation yield of radioiodine amounting to 90 ± 5 % and its decontamination factor from the Te and Sb radionuclides to ~104. The optimized separation method developed was then applied to the production of 124I via the 121Sb(α,n)124I process using a highly enriched 121Sb target. Quality control tests showed that the separated 124I occurred >99 % as iodide and the longer lived impurities 126I and 125I amounted to 0.16 % and <0.05 %, respectively. The trace level of inactive Sb impurity was determined by ICP–OES. 相似文献
177.
5‐O‐Caffeoylshikimic acid from Solanum somalense leaves: Advantage of centrifugal partition chromatography over conventional column chromatography 下载免费PDF全文
Saïda Chideh Serge Pilard Jacques Attoumbré Robert Saguez Alshaimaa Hassan‐Abdallah Dominique Cailleu Anne Wadouachi Sylvie Baltora‐Rosset 《Journal of separation science》2014,37(17):2331-2339
Solanum somalense leaves, used in Djibouti for their medicinal properties, were extracted by MeOH. Because of the high polyphenol and flavonoid contents of the extract, respectively, determined at 80.80 ± 2.13 mg gallic acid equivalent/g dry weight and 24.4 ± 1.01 mg quercetin equivalent/g dry weight, the isolation and purification of the main polyphenols were carried out by silica gel column chromatography and centrifugal partition chromatography. Column chromatography led to 11 enriched fractions requiring further purification, while centrifugal partition chromatography allowed the easy recovery of the main compound of the extract. In a solvent system composed of CHCl3/MeOH/H2O (9.5:10:5), 21.8 mg of this compound at 97% purity was obtained leading to a yield of 2.63%. Its structure was established as 5‐O‐caffeoylshikimic acid by mass spectrometry and NMR spectroscopy. This work shows that S. somalense leaves contain very high level of 5‐O‐caffeoylshikimic acid (0.74% dry weight), making it a potential source of production of this secondary metabolite that is not commonly found in nature but could be partly responsible of the medicinal properties of S. somalense leaves. 相似文献
178.
Nada F. Atta Hagar K. Hassan Ahmed Galal 《Analytical and bioanalytical chemistry》2014,406(27):6933-6942
A hybrid of reduced graphene oxide–palladium (RGO–Pd) nano- to submicron-scale particles was simultaneously chemically prepared using microwave irradiation. The electrochemical investigation of the resulting hybrid was achieved using cyclic voltammetry and differential pulse voltammetry. RGO–Pd had a higher current response than unmodified RGO toward the oxidation of morphine. Several factors that can affect the electrochemical response were studied, including accumulation time and potential, Pd loading, scan rate, and pH of electrolyte. At the optimum conditions, the concentration of morphine was determined using differential pulse voltammetry in a linear range from 0.34 to 12 μmol L?1 and from 14 to 100 μmol L?1, with detection limits of 12.95 nmol L?1 for the first range. The electrode had high sensitivity toward morphine oxidation in the presence of dopamine (DA) and of the interference compounds ascorbic acid (AA) and uric acid (UA). Electrochemical determination of morphine in a spiked urine sample was performed, and a low detection limit was obtained. Validation conditions including reproducibility, sensitivity, and recovery were evaluated successfully in the determination of morphine in diluted human urine. 相似文献
179.
180.
Hadisi Maliheh Vosoughi Naser Yousefnia Hassan Bahrami-Samani Ali Zolghadri Samaneh Vosoughi Sara Alirezapour Behrouz 《Journal of Radioanalytical and Nuclear Chemistry》2022,331(2):841-849
Journal of Radioanalytical and Nuclear Chemistry - In this study, optimized preparation, quality control, cell assessments and biostribution of 188Re-HYNIC-PSMA in normal rats and tumor bearing... 相似文献