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排序方式: 共有464条查询结果,搜索用时 15 毫秒
1.
Jai Kumar Singhal 《Pramana》2004,62(5):1029-1040
We examine the effects of mixing induced light heavy charged lepton neutral currents on the partial wave amplitude for the
process l+l− →ZZ (withl = e,μ or τ). By imposing the constraints that the amplitude should not exceed the perturbative unitarity limit at high energy (√s
= Λ), we obtain bounds on light heavy charged lepton mixing parameter sin2(2θ
L
a
) where θ
L
a
is the mixing angle of the ordinary charged lepton with its exotic partner. For Λ = 1 TeV, no bound is obtained on sin2 (2θ
L
a
) form
E < 0.69 TeV. However, sin2 (2θ
L
a
) ≤ 1.52×10−5 form
E = 5 TeV, sin2 (2θ
L
a
) ≤ 2.41 ×10−7 form
E = 10 TeV. Similarity for Λ = ∞ no bound is obtained on sin2 (2θ
L
a
) for mE < 1.97 TeV and sin2 (2θ
L
a
) ≤ 0.15 form
E = 5 TeV and sin2 (2θ
L
a
) ≤ 3.88×10-2 form
E = 10 TeV. 相似文献
2.
Transverse flow transversely excited (TFTE) CO2 lasers are easily scalable to multikilowatt level. The laser power can be scaled up by increasing the volumetric gas flow
and discharge volume. It was observed in a TFTE CW CO2 laser having single row of pins as an anode and tubular cathode that the laser power was not increasing when the discharge
volume and the gas volumetric flow were increased by increasing the electrode separation keeping the gas flow velocity constant.
The discharge voltage too remained almost constant with the change of electrode separation at the same gas flow velocity.
This necessitated revision of the scaling laws for designing this type of high power CO2 laser. Experimental results of laser performance for different electrode separations are discussed and the modifications
in the scaling laws are presented. 相似文献
3.
Chae Kyu Kim Eun Seok Song Hyung Joo Kim Chiyoung Park Young Chul Kim Jai Kyeong Kim Jae Woong Yu Chulhee Kim 《Journal of polymer science. Part A, Polymer chemistry》2006,44(1):254-263
We have synthesized conjugated dendrimer with triazine peripheries, and their luminescence properties were investigated. The dendrimers consist of dendritic triazine wedges for electron transport, distyrylbenzene core as an emitting moiety, and t‐butyl peripheral groups for good processing properties. The dendrimers have LUMO values of about ?2.7 eV possibly because of the triazine moiety with high electron affinity. Photoluminescence study indicates that energy transfer occurs from the triazine wedges to the stilbene bridge, and finally to the core chromophore units due to a cascade decrease of bandgap from the peripheral wedge to core moiety. Therefore, the emission wavelength was determined by the structure of the core unit. The energy transfer efficiency of distyrylbenzene‐cored dendrimers was about 75 and 55% for Trz‐1GD‐DSB and Trz‐2GD‐DSB, respectively. A preliminary electroluminescence property also was investigated. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 254–263, 2006 相似文献
4.
Pathak JA Davis MC Hudson SD Migler KB 《Journal of colloid and interface science》2002,255(2):391-402
We investigate the influence of confinement on the steady state microstructure of emulsions sheared between parallel plates, in a regime where the average droplet dimension is comparable to the gap width between the confining walls. Utilizing droplet velocimetry, we find that the droplets can organize into discrete layers under the influence of shear. The number of layers decreases from two (at relatively higher shear rates) to one (at lower shear rates), as the drops grow slightly larger due to coalescence. We argue that the layering and overall composition profile may be controlled by the interplay of droplet collisions (which can cause separation of droplet centers in the velocity gradient direction), droplet migration toward the centerline (due to wall effects), and droplet packing constraints. We also study the effects of mixture composition on droplet microstructure, and summarize these results in the form of a morphology diagram in the parameter space of mass fraction and shear rate. We find that formation of strings of the suspended phase (reported earlier by our group in flow-visualization studies on confined emulsions) is observed over a broad composition window. We also find a stable (nontransient) morphology wherein the droplets are arranged in highly ordered pearl-necklace chain structures. 相似文献
5.
T.?L.?Shanker Rao K.?N.?Lad A.?PratapEmail author 《Journal of Thermal Analysis and Calorimetry》2004,78(3):769-774
The crystallization kinetics of amorphous Cu50Ti50 has been studied using differential scanning calorimetry (DSC) under non-isothermal conditions. The curves at different linear heating rates (2, 4, 8 and 16 K min–1) show sharp crystallization peaks. The crystallization peak shifts to higher temperatures with increasing heating rate. The Kissingers method of analysis of the shift in the transformation peak is applied to evaluate the activation energy (E
c). The KJMA formalism, which is basically developed for isothermal experiments, is also used to obtain E
c and the Avrami parameter (n).The DSC data have been analysed in terms of kinetic parameters, viz. activation energy (E
c), Avrami exponent (n) and frequency factor K
0 using three different theoretical models. It is observed that the activation energy values derived from KJMA approach and modified Kissinger equation agree fairly well with each other. The activation energy values obtained from normal Kissinger method, and Gao and Wang expression underestimate the activation energy.The financial support provided by All India Council for Technical Education (AICTE), New Delhi (Govt. of India) is gratefully acknowledged. 相似文献
6.
The problem of calculating the thermodynamic properties of two-dimensional semiclassical hard-body fluids is studied. Explicit expressions are given for the first-order quantum corrections to the free energy, equation of state, and virial coefficients. The numerical results are calculated for the planar hard dumbbell fluid. Significant features are the increase in quantum corrections with increasing eta and increasing L*=L/sigma(0). 相似文献
7.
Cytochrome P-450 isozymes represent a critical component of nature’s spectrum of detoxification catalysts that could be exploited
for bioremediation. The ethanol-inducible human cytochrome P-450 2E1 serves as a model eukaryotic P-450 that complements the
bacterial P-450 cam in dehalogenation and detoxification of environmental pollutants. We explored the construction of novel
chimeric P-450s using cytochrome P-450 camC and 2E1 genes. For construction of chimera 1 (478 amino acids, 55.14 kDa), 145 amino acids from the N-terminus of P-450 2E1 protein
(493 amino acids, 56.84 kDa) were replaced with 130 amino acids from the N-terminus of P-450 camC protein (415 amino acids,
46.66 kDa). In chimera 2 (525 amino acids, 60.24 kDa) the strategy involves replacement of 28 amino acids in the C-terminus
of chimera 1 with 75 amino acids from the C-terminus of P-450 camC gene. Homology models of both the chimeric proteins were
developed using SWISS-MODEL based on the known crystal structure of cytochrome P-450 camC, BM-3, 1DT6A, and 2C17A. The models
indicated that the proposed heme-binding site was intact, which is inevitable for catalytic activity of cytochrome P-450s.
The expression of chimera 1 and 2 genes in Escherichia coli DH5α was evident from light-pink cell pellets, protein band in sodium dodecyl sulfate polyacrylamide gel electrophoresis,
and diagnostic carbon monoxide-difference spectra. Our studies show that strategies can be developed to exploit the natural
diversity of the P-450 superfamily to generate chimeric biocatalysts that would provide new templates amenable to directed
evolution. 相似文献
8.
The diffusion length of charge carriers in the active layer of a perovskite solar cell (PSC) of the structure Glass/PEDOT: PSS/CH3NH3PbI3/PC60BM/Al is modelled. It is found that the diffusion length depends on the position x in the active layer measured from the PEDOT: PSS interface, Urbach energy and temperature. By varying the voltage in the range from zero to , it is shown that the dependence of diffusion length on the position x in the active layer reduces at higher voltage. The combined influence of applied voltage and temperature on the diffusion length of charge carriers is investigated and it is found that in the low voltage range the diffusion length is temperature independent, but it becomes significantly temperature dependent at higher voltages. Also, it is found that the diffusion length decreases as the applied voltage increases and this reduction becomes much more significant at higher voltage and temperatures. The combined influence of applied voltage and Urbach energy on diffusion length of charge carriers reveals that the diffusion length decreases when both the applied voltage and Urbach energy increase. However, the reduction in the diffusion length due to the increase in Urbach energy becomes less significant at higher voltage. 相似文献
9.
In developing a method for possible low level isotopic enrichment, which uses to advantage the equilibrium isotope effect
observed during U(1V)-U(VI) electron exchange reaction in sulphate solutions, details of a solvent extraction process involving
high concentration of a mixture of U(IV) and U(VI) and at low acid concentrations, are described. The extraction behaviour
of uranium under these conditions is discussed. During the extraction with amines, U(IV) tended to get oxidised in sulphate
solutions. 相似文献
10.
Summary The coagulation concentration for a titania sol decreases if the concentration of a mixture of electrolytes and papain decreases. If the concentration of papain is increased then lesser amount of electrolytes is needed to coagulate the sol. If glycine is added as an additional substance then the value decreases more rapidly. There is no significant change in the pH and the electrical conductance of the sol by the addition of papain or electrolytes. There is a little change, when glycine is added as an additional substance. These observations are explained due to the formation of negative papain ions in a low pH region. The possibility of the adsorption or the release of the counter ions is ruled out.The authors wish to thank Dr.R. C. Mehrotra, Professor and the Head of the Chemistry Department for providing all the facilities for this work. We are also thankful to the Ministry of Education, Government of India, for the award of a research scholarship to one of us (V.K.S.). 相似文献