排序方式: 共有56条查询结果,搜索用时 15 毫秒
21.
We examine the electronic structure of nanostructured nickel oxide with an average particle size of 4–5nm using Ni 2p X-ray photoelectron spectrum. The most striking features of the spectrum are the Ni 2p main line broadening and an increase in the relative intensity of the 1.5eV satellite. We explain the observations as due to an enhancement in the non-local screening process on the basis of Ni7O36 cluster model by taking into account the large surface area to volume ratio and high Ni2+ vacancy concentration in nanostructured nickel oxide. The important contribution of an enhanced Ni 3d–O 2p hybridization and the origin of shake-up peaks above the 7eV satellite is also discussed. The study underlines the importance of factors such as the actual local environment of the core hole site, defect density and distribution, possible structural transitions, etc. in determining the Ni 2p core level X-ray photoelectron spectrum of nanostructured nickel oxide and shows that the actual synthesis routes and the thermal history greatly influence the electronic structure of nanostructured nickel oxide. 相似文献
22.
García Ruano JL Gamboa AE Gutiérrez LG Martín Castro AM Rodríguez Ramos JH Yuste F 《Organic letters》2000,2(6):733-736
A new kind of chiral dienophiles, cyclic vinyl-p-tolylsulfilimines (2a and 2b), were obtained from the corresponding (Z)-sulfinylacrylonitriles with HBF(4) and methanol. The asymmetric Diels-Alder reaction of optically pure 2a with cyclopentadiene under mild thermal or catalyzed conditions afforded only the endo-4a adduct with complete endo and pi-facial selectivities. The ability of the sulfilimine moiety to enhance the dienophilic reactivity of the double bond is similar to that of the sulfinyl group. 相似文献
23.
Acoustic non-linearity parameter B/A is calculated for binary mixtures using four different methods. The interactions in the liquid mixtures are explained on the basis of excess non-linearity parameter and excess adiabatic compressibility. Sehgal's relations for calculating molecular properties of pure liquids are extended to binary mixtures. 相似文献
24.
Nanocrystals of calcium tungstate (CaWO4) of three different grain sizes were synthesized through chemical precipitation technique and the grain sizes and crystal structure were determined using the broadening of X‐ray diffraction patterns and transmission electron microscopy. The microhardness of compacted pellets of nanocrystalline calcium tungstate (CaWO4) with different grain sizes were measured using a Vickers microhardness tester for various applied loads ranging from 0.049 N to 1.96 N. The values of microhardness showed significant reverse indentation size effect at low indentation loads. The microhardness data obtained for samples of different grain sizes showed grain size dependent strengthening obeying normal Hall‐Petch relation. The dependence of compacting pressure and annealing temperature on microhardness of the nanostructured sample with grain size of 13 nm were also studied. The samples showed significant increase in microhardness as the compacting pressure and annealing time were increased. (© 2008 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim) 相似文献
25.
26.
27.
Simultaneous determination of titanium and molybdenum in steel samples using derivative spectrophotometry in neutral micellar medium 总被引:2,自引:0,他引:2
Varghese A Khadar AM Kalluraya B 《Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy》2006,64(2):383-390
A simple, selective and sensitive spectrophotometric method has been developed for the individual and simultaneous determination of Ti(IV) and Mo(VI) using resacetophenone p-hydroxybenzoylhydrazone (RAPHBH) in presence of Triton X-100, without any prior separation. Beer's law is obeyed between 0.13-1.2 microg mL-1 and 0.18-1.90 microg mL-1 concentration of Ti(IV) and Mo(VI) at 455 nm and 405 nm, respectively. The molar absorptivity and Sandell's sensitivity of the coloured complexes at pH 3.0 are 3.1x10(4) L mol-1 cm-1, 4.2x10(4) L mol-1 cm-1, and 1.6 ng cm-2, 2.3 ng cm-2 for Ti(IV) and Mo(VI), respectively. The stoichiometry of the complexes were found to be 1:2 and 1:1 (metal:ligand) for Ti(IV) and Mo(VI), respectively. These metal ions interfere with the determination of each other in zero-order spectrophotometry. The first derivative spectra of these complexes permitted a simultaneous determination of Ti(IV) and Mo(VI) at zero crossing wavelengths of 500.0 nm and 455.0 nm, respectively. The effect of foreign ions in the determination of Ti(IV) and Mo(VI) were investigated. The proposed method has been successfully applied for the determination of titanium and molybdenum in standard alloy steel, mineral and soil samples. 相似文献
28.
29.
Munshi G Mustafa Sudhir Raniwala T Awes B Rai RS Bhalerao JG Contreras RV Gavai SK Ghosh P Jaikumar GC Mishra AP Mishra H Mishra B Mohanty J Nayak J-Y Ollitrault SC Phatak L Ramello R Ray PK Sahu AM Srivastava DK Srivastava VK Tiwari 《Pramana》2006,67(5):961-981
This is the report of Heavy Ion Physics and Quark-Gluon Plasma at WHEPP-09 which was part of Working Group-4. Discussion and
work on some aspects of quark-gluon plasma believed to have created in heavy-ion collisions and in early Universe are reported. 相似文献
30.
AM Cardoso SM Alexandre CM Barros AJ Correia NM Nibbering 《Rapid communications in mass spectrometry : RCM》1999,13(19):1885-1888
The collision-induced dissociation (CID) of deprotonated arylalkylamines of general formula R(1)C(6)H(4)CHR(2)CH(2)NR(3)(2) (where R(1) = H, OH, F or NO(2); R(2) = H or OH; R(3) = H or CH(3)) generated by negative chemical ionization with H(2)O and D(2)O as ionizing reagents, is discussed. The negative chemical ionization mass spectra show that, in the absence of a hydroxy group in the aromatic ring, deprotonation takes place at the benzylic position whereas the proton is lost from the OH group when present. The nitro compound forms only M(-.) ions. The CID spectra of the deprotonated molecules show that fragmentations are strongly dependent on the structural features of the molecules, namely the presence or absence of substituents in the aromatic ring or aliphatic chain. Copyright 1999 John Wiley & Sons, Ltd. 相似文献