In the present research, magnesium aluminate spinel was prepared as catalyst support using a novel, facile, and efficient mechanochemical method. The Co-promoted catalysts with 20 wt.% of Ni were fabricated using an impregnation route and the samples were analyzed by the X-ray diffraction (XRD), N2 adsorption/desorption (BET), temperature-programmed reduction and desorption (H2-TPR and O2-TPD), and field emission scanning electron microscopy (FESEM) tests. The results confirmed that all samples have a mesoporous structure with a high specific surface area and the presence of cobalt caused complete CH4 oxidation at low temperatures, and no side reactions were observed. The results indicated that the 3%Co-20%Ni/MgAl2O4 catalyst was the optimal sample among the prepared catalysts, owing to the improvement of reduction features and oxygen mobility. The 50 and 90% of methane conversion was obtained at 530 and 600 °C, respectively. Also, the influence of calcination temperature, GHSV, and feed ratio was determined on the catalytic activity. The obtained outcomes revealed that the calcination temperature has a significant effect on the textural properties and catalytic efficiency. The sample calcined at 700 °C showed the weakest performance, which was related to the sintering of particles at high temperatures. The catalytic stability showed that the 3%Co-20%Ni/MgAl2O4 has acceptable stability during 600 min time of reaction.
We demonstrate a three orders of magnitude increase and stability in the backscattered fluorescence signal from nitrogen molecules
by terawatt femtosecond laser pulse induced air filaments using a new method. The method is based on squeezing the initial
beam diameter using a telescope. The effect of laser shot-to-shot fluctuations was included in numerical simulations by a
random distribution of the initial intensity in both squeezed and non-squeezed beams. Statistical processing of the simulation
results shows that the average diameter of plasma channels as well as the total amount of free electrons generated in a bunch
of multiple filaments in air is larger in the squeezed beam. Shot-to-shot stability of the simulated plasma density increases
in the squeezed beam. The change of this plasma density with propagation distance is in good qualitative agreement with the
change of the range-corrected nitrogen fluorescence signal with distance.
PACS 42.65.Jx; 42.60.Jf; 42.68.Ay; 42.68.Wt 相似文献
Several planar waveguides have been fabricated. The waveguides have been polished for determination of their refractiveindex profiles (RIP) by wedge method. The RIP determined by inserting the sample in a Mach-Zehnder interferometer andapplying fringe analysis methods. 相似文献
Enthalpies of mixing (mH) aqueous solutions of CoCl2, CuCl2, and MnCl2 with NaCl solutions were measured at constant ionic strengths of 0.5, 1.0, and 3.0 molal at 25°C. The excess enthalpy equations of Pitzer were then fit to the resulting mH data. The resulting parameters are the temperature derivatives of the activity coefficient mixing parameters in the Pitzer system. The heat of mixing data for CoCl2 and CuCl2 were in agreement with earlier isomolal results by other workers. 相似文献
Headspace solvent microextraction (HSME) into a single drop is developed for the determination of six trihalomethanes, CH2Cl2, CHCl3, C4H9Cl, CCl4, C2HCl3, and C2Cl4, in aqueous solution. A drop of benzyl alcohol containing bromoform, as an internal standard, is used for extraction. The analytes are extracted by suspending a 3-microL drop directly from the needle of a microsyringe. The needle passes through the septum of a vessel, and the needle tip appears above the surface of the solution. After the prescribed extraction time, the drop is drawn back into the syringe. The syringe is then removed, and its content is injected directly into a gas chromatography column for analysis. The main parameters affecting the HSME process, such as stirring speed, microdrop volume, sample solution temperature, microsyringe needle temperature, sample volume, solution pH, extracting solvent, and ionic strength of the solution, are studied. Also, the linear range and precision of the method are examined. 相似文献
A satisfactory method was described for separation and preconcentration of ultratrace amounts of fluoride ions enriched by
zirconia (ZrO2) as an inorganic ion exchanger. Fluoride ions can be adsorbed rapidly and selectively on zirconia from an acidic solution
(pH 4.8) then reversibly desorbed by increasing pH up to 13. A flow system consisting of a column packed with zirconia impregnated
on cellulose fibers and an ion-selective electrode was used for the determination of fluoride. The RSD was found to be 1.6%
and the detection limit defined by S/N = 3 was 3 × 10−9 mol L−1. The interference effects of various ions, such as nitrate, sulfate, halides, alkaline, and alkaline earth ions, which may
be found in the environmental water, were studied, and it was found that they were tolerated even at high concentrations.
The method was applied to determine fluoride in drinking water, which contains ultratrace amounts of fluoride. The concentration
of fluoride was found to be 42 μg L−1, which is confirmed by spiking 2 μmol fluoride to the drinking water with a recovery of 99%.
Published in Russian in Zhurnal Analiticheskoi Khimii, 2006, Vol. 61, No. 2, pp. 179–183.
The text was submitted by the authors in English. 相似文献
Some new N‐carbonyl, phosphoramidates with formula C6H5C(O)N(H)P(O)R2 (R = NC3H6 ( 1 ), NC6H12 ( 2 ), NHCH2CH=CH2 ( 3 ), N(C3H7)2 ( 4 )) and CCl3C(O)N(H)P(O)R′2 (R′ = NC3H6 ( 5 ), NHCH2CH=CH2 ( 6 )) were synthesized and characterized by 1H, 13C, 31P NMR and IR spectroscopy and elemental analysis. The structures were determined for compounds 1 and 2 . Compound 1 exists as two crystallographically independent molecules in crystal lattice. Both compounds 1 and 2 produced dimeric aggregates via intermolecular ‐P=O…H‐N‐ hydrogen bonds, which in compound 2 is a centrosymmetric dimer. In compounds with four‐membered ring amine groups, 3J(P,C)>2J(P,C), in agreement with our previous studies about five‐membered ring amine groups. Also, 3J(P,C) values in compounds 1 and 5 are greater than in compounds with five‐, six‐ and seven‐membered ring amine groups. 相似文献