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排序方式: 共有474条查询结果,搜索用时 15 毫秒
1.
K. Kaya K. Fuke S. Nonose N. Kikuchi 《Zeitschrift für Physik D Atoms, Molecules and Clusters》1989,12(1-4):571-573
Aluminum clusters were generated by a laser vaporization method. Ionization potential of Al2 was found to be lower than that of Al. In the reaction with oxygen at high concentration, the mixed cluster Al9O7 survives predominantly as a stable cluster. Ammonia was found to be adsorbed weakly on the Aln surface. 相似文献
2.
Vnira R. Akhmetova Guzel R. Nadyrgulova Tat'yana V. Tyumkina Mikhail Yu. Antipin Usein M. Dzhemilev 《Tetrahedron》2007,63(47):11702-11709
Cyclocondensation of aliphatic diamines with CH2O and H2S (1:3:2 ratio, 0 °C) was carried out to give thiadiazabicyclanes and dithiadiazabicyclanes (1:6:4 ratio), which were previously difficult to synthesize. Symmetric α,ω-bis-1,3,5-dithiazinanes were synthesized at 80 °C by this reaction. The stereochemistry of thiadiazabicyclanes was assigned by 1H and 13C NMR spectroscopy and by theoretical DFT calculations, and of bis-dithiazinanes by X-ray diffraction study in the solid state. 相似文献
3.
Tsuyoshi Kurikawa Hiroaki Takeda Atsushi Nakajima Koji Kaya 《Zeitschrift für Physik D Atoms, Molecules and Clusters》1997,40(1):65-69
In the gas phase, we have successfully synthesized organometallic clusters, Mn(benzene)m (M=3d transition metal atoms), by using a laser vaporization method. The measurements of mass spectra and ionization energies (Ei) have revealed that the organometallic clusters can take two types of structures; layered sandwich structures (m = n + 1) and metal clusters saturatedly covered with benzenes. For early transition metals of Sc, Ti, and V, only the multiple decker sandwich structure clusters were preferentially produced, in which benzene and metal atoms are alternately piled up. For late transition metals of Co and Ni, the metal clusters saturatedly surrounded by benzenes were also produced as well as the sandwich clusters. Furthermore, the Eis of M1(benzene)2 (M = Sc-Ni) were systematically measured and their electronic properties will be discussed. 相似文献
4.
The effect of diffusion on radiation-initiated graft polymerization has been studied with emphasis on the single- and two-penetrant cases. When the physical properties of the penetrants are similar, the two-penetrant problem can be reduced to the single-penetrant problem by redefining the characteristic parameters of the system. The diffusion-free graft polymerization rate is assumed to be proportional to the v power of the monomer concentration C, in which the proportionality constant a = kpR/k, where kp and kt are the propagation and termination rate constants, respectively, and Ri is the initiation rate. The values of v, w, and z depend on the particular reaction system. The results of our earlier work were generalized by allowing a non-Fickian diffusion rate, obtained from an extension of the Fujita free-volume theory, which predicts an essentially exponential dependence on the monomer concentration of the diffusion coefficient, D = D0 [exp(δC/M)], where M is the saturation concentration. It was shown that a reaction system is characterized by the three dimensionless parameters v, δ, and A = (L/2)[aM(v?1)/D0]1/2, where L is the polymer film thickness. Graft polymerization tends to become diffusion controlled as A increases. Larger values of δ and v cause a reaction system to behave closer to the diffusion-free regime. The transition from diffusion-free to diffusion-controlled reaction involves changes in the dependence of the reaction rate on film thickness, initiation rate, and monomer concentration. Although the diffusion-free rate is w order in initiation rate, v order in monomer, and independent of film thickness, the diffusion-controlled rate is w/2 order in initiator rate and inverse first-order in film thickness. The dependence of the diffusion-controlled rate on monomer is dependent in a complex manner on the diffusional characteristics of the reaction system. 相似文献
5.
Frequency and voltage-dependent electrical and dielectric properties of Al/Co-doped PVA/p-Si structures at room temperature 下载免费PDF全文
In order to investigate of cobalt-doped interracial polyvinyl alcohol (PVA) layer and interface trap (Dit) effects, A1/p- Si Schottky barrier diodes (SBDs) are fabricated, and their electrical and dielectric properties are investigated at room temperature. The forward and reverse admittance measurements are carded out in the frequency and voltage ranges of 30 kHz-300 kHz and -5 V-6 V, respectively. C-V or er-V plots exhibit two distinct peaks corresponding to inversion and accumulation regions. The first peak is attributed to the existence of Dit, the other to the series resistance (Rs), and interfacial layer. Both the real and imaginary parts of dielectric constant (er and err) and electric modulus (Mr and Mrr), loss tangent (tan~), and AC electrical conductivity (aac) are investigated, each as a function of frequency and applied bias voltage. Each of the M~ versus V and Mrr versus V plots shows a peak and the magnitude of peak increases with the increasing of frequency. Especially due to the Dit and interfacial PVA layer, both capacitance (C) and conductance (G/w) values are strongly affected, which consequently contributes to deviation from both the electrical and dielectric properties of A1/Co-doped PVA/p-Si (MPS) type SBD. In addition, the voltage-dependent profile of Dit is obtained from the low-high frequency capacitance (CLF-CHF) method. 相似文献
6.
7.
Three-phase partitioning (TPP) was used to purify and recover catalase from potato crude extract. The method consists of ammonium sulfate saturation, t-butanol addition, and adjustment of pH, respectively. The best catalase recovery (262 %) and 14.1-fold purification were seen in the interfacial phase in the presence of 40 % (w/v) ammonium sulfate saturation with 1.0:1.0 crude extract/t-butanol ratio (v/v) at pH 7 in a single step. The sodium dodecyl sulfate–polyacrylamide gel electrophoresis (SDS-PAGE) analysis of the enzyme showed comparatively purification and protein molecular weight was nearly found to be 56 kDa. This study shows that TPP is a simple, economical, and quick method for the recovering of catalase and can be used for the purification process. 相似文献
8.
The fast transient fluorescence (FTRF) technique was used to study critical exponents at the glass transition in free-radical crosslinking copolymerization (FCC) for two different monomeric systems, methyl methacrylate (MMA) and styrene (S). Pyrene (Py ) was used as a fluorescence probe. The fluorescence lifetimes of Py from its decay traces were measured and used to monitor the gelation process. Changes in the viscosity of the pregel solutions due to glass formation dramatically enhance the fluorescent yield of aromatic molecules. This effect is used to study the glass transition upon gelation of MMA and S monomeric systems as a function of time, at various temperatures and crosslinker concentrations. The results are interpreted in the view of percolation theory. The gel fraction and weight average degree of polymerization exponents β and γ are found to be 0.37 ± 0.02 and 1.66 ± 0.07 in agreement with percolation results. 相似文献
9.
Hilal Goktas Dogan Mansuroglu Betul Atalay Sinan Bilikmen Ismet Kaya 《Plasma Chemistry and Plasma Processing》2012,32(1):35-44
The synthesis of polyfluorene (PF) thin films by simultaneously superposing a continuous and pulsed discharge and the characterizations
of these samples are presented. The double discharge plasma system is constructed by superposing two discharges; namely, a
low pressure dc glow one and a high current pulsed one. The fluorene monomer in powder form was vaporized in the system at
argon plasma without any modification, at 0.5 mbar operating pressure. The structure of the thin films was investigated via
XPS, UV–visible, FTIR, XRD and SEM. The FTIR and the UV–visible results revealed that the fluorene structure was retained
at the produced samples. Semi-conducting behavior was established, and upon the iodine doping, the optical energy band gap
(E
g
) dropped down from 3.7 to 2.4 eV. The morphology of the synthesized PF thin films was amorphous, with granular structures
of different sizes depending on the location of the substrate. 相似文献
10.
The transport of Hg (II) ions from an aqueous solution into an aqueous receiving solution through bulk and supported liquid membranes containing a calix[4]arene derivative 1 as a carrier was examined. The kinetic parameters of bulk liquid membrane studies were analyzed assuming two consecutive, irreversible first‐order reactions. The influence of temperature, stirring rate, carrier concentration and solvent on the kinetic parameters (k1, k2, Rm max, tmax, Jd max, Ja max) has also been investigated. The membrane entrance rate, k1, and the membrane exit rate, k2, increased with increasing temperature and stirring rate. The activation energy values are calculated as 4.87 and 48.63 kj mol?1 for extraction and reextraction, respectively. The values of calculated activation energy indicate that the process is diffusionally controlled by species. Also, the transport behavior of Hg2+ from aqueous solution through a flat‐sheet supported liquid membrane has been investigated by the use of calix[4]arene derivative 1 as carrier and Celgard 2500 as the solid support. A Danesi mass transfer model was used to calculate the permeability coefficients for each parameter studied. The highest values of permeability were obtained with 2‐nitrophenyloctyl‐ether (NPOE) solvent and the influence was found to be in the order of NPOE>chloroform>xylene. 相似文献