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961.
在添加了15%Li_2O的NdMO_3(M=Cr、Mn、Fe、Co、Ni)上进行了甲烷氧化偶联(OCM)反应研究.通过改变反应气中CH_4:O_2浓度比,在氧化态和“脱氧态”催化剂上的CH_4脉冲反应,探讨了表面吸附氧和晶格氧在OCM反应中的作用以及NdMO_3中不同金属离子(M)对OCM反应活性的影响等. 相似文献
962.
In this paper an algorithm is developed to generate all nondominated extreme points and edges of the set of objective values of a multiple objective linear program. The approach uses simplex tableaux but avoids generating unnecessary extreme points or bases of extreme points. The procedure is based on, and improves, an algorithm Dauer and Liu developed for this problem. Essential to this approach is the work of Gal and Kruse on the neighborhood problem of determining all extreme points of a convex polytope that are adjacent to a given (degenerate) extreme point of the set. The algorithm will incorporate Gal's degeneracy graph approach to the neighborhood problem with Dauer's objective space analysis of multiple objective linear programs. 相似文献
963.
964.
This paper considers an optimal boundary control problem fora hyperbolic system in which constant time lags appear in thestate equation and in the boundary condition simultaneously.Making use of Lion's scheme, necessary and sufficient conditionsof optimality for the Neumann problem are derived. 相似文献
965.
We present anO(p · n) algorithm for the problem of finding disjoint simple paths of minimum total length betweenp given pairs of terminals on oriented partial 2-trees withn nodes and positive or negative arc lengths. The algorithm is inO(n) if all terminals are distinct nodes. We characterize the convex hull of the feasible solution set for the casep=2.We gratefully acknowledge the referee's many helpful suggestions to improve the presentation of this paper. 相似文献
966.
双参数变形玻色湮没算符高次幂的本征态及其量子统计性质 总被引:1,自引:1,他引:0
本文构造了双参数变形玻色湮没算符高次幂a'k(k≥3)的k个正交归一木征态的数学结构,发现它们能构成一个完备的Hilbert空间,并且讨论了它们的量子统计性质. 相似文献
967.
P. Guenoun M. Delsanti D. Gazeau J.W. Mays D.C. Cook M. Tirrell M. Tirrell L. Auvray 《The European Physical Journal B - Condensed Matter and Complex Systems》1998,1(1):77-86
Aqueous micellar solutions of ionic/neutral block copolymers have been studied by light scattering, small angle neutron scattering
and small angle X-ray scattering. We made use of a polymer comprised of a short hydrophobic block (polyethylene-propylene)
PEP and of a long polyelectrolytic block (polystyrene-sulfonate) PSSNa which has been shown previously to micellize in water.
The apparent polydispersity of these micelles is studied in detail, showing the existence of a few large aggregates coexisting
with the population of micelles. Solutions of micelles are found to order above some threshold in polymer concentration. The
order is liquid-like, as demonstrated by the evolution with concentration of the peak observed in the structure factor (), and the degree of order is found to be identical over a large range of concentrations (up to 20 wt%). Consistent values
of the aggregation number of the micelles are found by independent methods. The effect of salt addition on the order is found
to be weak.
Received: 19 June 1997 / Received in final form: 4 September 1997 / Accepted: 9 October 1997 相似文献
968.
A diode-end-pumped Nd:YAG laser is passively Q-switched by using Cr4+:YAG as saturable absorber. When CW pumped with a laser diode which the maximum power is 550 mW, the laser produces pulses of 24 ns duration at 1064 nm, with an energy of 26 μJ. 相似文献
969.
I. P. Romanova S. G. Fattakhov A. A. Nafikova I. I. Vandyukova R. R. Shagidullin N. M. Azancheev V. S. Reznik O. G. Sinyáshin 《Russian Chemical Bulletin》1998,47(9):1812-1819
The reactions of phosphine derivatives of diallyl isocyanurates with palladium(ii) dichloride lead to the formation of complexes, whose structure, composition, and stability depend on the length of the methylene
chain between the isocyanurate and diphenylphosphine fragments in the ligand. 1,3-Diallyl-5-[5′-(diphenylphosphino)pentyl
and 10′-(diphenyl-phosphino)decyl] isocyanurates with PdCl2 form monomeric L2PdCl2
trans-complexes in which P atoms of the ligands participate in coordination with the metal. 1,3-Diallyl-5-[2′-(diphenylphosphino)ethyl]
isocyanurate with PdCl2 forms a dimeric (LPdCl2)2 complex, which decomposes in a solution to the monomer including solvent molecule into the coordination sphere of the metal.
The reactions of 1,3-diallyl-5-[4′-(diphenylphosphino)butyl] isocyanurate and 1,3-diallyl-5-[6′-(diphenylphosphino)hexyl]
isocyanurate with PdCl2 give monomeric chelate LPdCl2 complexes in which one of the allyl groups of the isocyanurate cycle participates in coordination with the central ion along
with the phosphorus atom.
Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 9, pp. 1859–1865, September, 1998. 相似文献
970.
Jon Samseth Richard J. Spontak Kell Mortensen 《Journal of Polymer Science.Polymer Physics》1993,31(4):467-474
Poly(siloxaneimide) (PSI) segmented copolymers exhibit organized microdomains if the blocks are sufficiently incompatible. As with neat diblock and triblock copolymers, the processing route employed to prepare films of PSI materials is expected to influence the dimensions and/or morphology of the resultant microstructure. In this work, small-angle neutron scattering (SANS) is utilized to characterize the disordered microstructure found in films of a series of PSI copolymers which are subjected to solvent casting and various thermal treatments. Microstructural dimensions such as the periodicity and correlation length are deduced from the Teubner-Strey (TS) model for disordered microemulsions. The scattering intensity of each copolymer up to q = 5.0 nm?1, where q is the scattering vector, is found to scale as q?2.8+?0.1. Results indicate that processing the materials as cast films or as melt-pressed films allowed to cool slowly has a small, but discernible, effect on microstructural characteristics. SANS profiles of films quenched from elevated temperatures reveal a clear transition in microdomain periodicity, which correlates well with the glass transition temperature of the imide microphase in these and other materials of similar chemical structure. © 1993 John Wiley & Sons, Inc. 相似文献