轻核中中子间的对相互作用和中子晕

选择Skyme势E作为两核子间唯象相互作用,在Hartree-Fock理论中结合粒子数守恒方法处理同类核子间的对相互作用,计算了Li和Be的丰中子同位素的结构,计算表明中子间的对相互作用和双中子晕之间存在紧密的联系.     

Difference in moments of inertia and paring interaction strength in superdeformed nuclei

The difference in the bandhead moments of inertia between the superdeformed (SD) band¹⁹⁴Hg(1) and the two-quasiparticle SD bands¹⁹⁴Hg(2, 3) was investigated using the particle-number-conserving treatment for the cranked shell model Hamiltonian. and the pairing interaction strength in SD nuclei is estimated to be much weaker than that in normally deformed nuclei.     

The quadrupole plus pairing interaction model in large configuration space for W,Os and Pt nuclei

The equilibrium deformations of tungsten, osmium and platinum nuclei are studied with the self-consistent quadrupole plus pairing interaction model by considering all the nucleons in nucleus explicitly. It is shown that similar results can be obtained by performing calculations with or without the assumption of an inert core. The only difference is in the strength of the quadrupole and pairing interactions to be employed in the respective calculations. The experimental static quadrupole moments and theB (E2) values are correctly reproduced by performing calculations with bare nucleon charge for all the nucleons.     

Conductance of tetraalkylammonium salts in propylene carbonate at 25°C

Conductance measurements of 12 quaternary ammonium salts in propylene carbonate (PC) have been made at 25°C. The cations were either tetramethylammonium, tetraethylammonium, or tetra-n-butylammonium, and the concentrations of salt varied from about 2×10^–4 to 5×10^–3 M. The data were analyzed by the equation of Pitts. The results showed that the benzoate, nitrobenzoate, and pentachlorophenolate salts are completely dissociated. The nitrophenolate, chlorophenolate, methylsulfonate, and nitrate salts are only slightly associated (K _A from 2.5 to 6.5), while the acetate, phenylacetate, and nitrophenolate salts display somewhat more extensive association, with ionpair association constants from 17 to 45. Limiting molar conductances for the anions were derived. The factors affecting ionic mobilities in this dipolar aprotic solvent are discussed.On leave 1973–1975 from the University of Gdask, Poland.     

Elliptic Curves Suitable for Pairing Based Cryptography

For pairing based cryptography we need elliptic curves defined over finite fields whose group order is divisible by some prime with where k is relatively small. In Barreto et al. and Dupont et al. [Proceedings of the Third Workshop on Security in Communication Networks (SCN 2002), LNCS, 2576, 2003; Building curves with arbitrary small Mov degree over finite fields, Preprint, 2002], algorithms for the construction of ordinary elliptic curves over prime fields with arbitrary embedding degree k are given. Unfortunately, p is of size .We give a method to generate ordinary elliptic curves over prime fields with p significantly less than which also works for arbitrary k. For a fixed embedding degree k, the new algorithm yields curves with where or depending on k. For special values of k even better results are obtained.We present several examples. In particular, we found some curves where is a prime of small Hamming weight resp. with a small addition chain.AMS classification: 14H52, 14G50     

Effect of the type of ion-pairing reagent in reversed-phase ion-pair chromatography

Summary The retention of positively and negatively charged and neutral solutes was studied in an aqueous phosphate buffer eluent, with constant inorganic-counterion concentration, on ODS-Hypersil stationary phase in the presence of various sulfonic acid ion-pairing reagents. The adsorption isotherms of the ion-pairing reagents d-camphor-10-sulfonic acid, sodium cyclohexylsulfamic acid and sodium alkylsulfonates (butyl-, hexyl- and octyl-) were determined by the breakthrough method.Dedicated to Professor J. F. K. Huber on the occasion of his 60th birthday.     

Divalent sulfate ion pairs in aqueous solutions at pressures up to 2000 atm

Electrical conductance measurements have been made at various temperatures and at concentrations from ca. 0.00005 to ca. 0.01M in aqueous solutions of MgSO₄, CaSO₄, CoSO₄ and NiSO₄ at pressures up to 2000 atm. The data have been analyzed with the Fernandez-Prini modification of the Fuoss-Hsia conductance equation to obtain the molal dissociation constants K _m at each pressure. The results for V^°, obtained from the pressure dependence ofK _m,are compared with other experimental data and with values calculated from acoustically derived multistate dissociation models.     

一种灵活的基于身份的签名方案

在基于身份的密钥提取过程中,使密钥生成器在私钥中嵌入随机数,从而使得密钥提取具有较好的灵活性,使得用户对一个身份可具备多个私钥,这无疑会增加密钥使用的安全性;基于这种新的密钥提取思路,给出一个基于身份的签名体制,新的密钥提取方式使得它具有更好的安全性和灵活性;新的基于身份的签名体制中具有最少对运算,因此,与类似的方案相比,其具备较好的计算效率;新签名体制的安全性依赖于k-合谋攻击问题(k-CAAP)的困难性,其在适应性选择消息和ID攻击下具备强不可伪造性,并且其安全性证明具有紧规约性.     

Maximal resolvable packings and minimal resolvable coverings of triples by quadruples

Determination of maximal resolvable packing number and minimal resolvable covering number is a fundamental problem in designs theory. In this article, we investigate the existence of maximal resolvable packings of triples by quadruples of order v (MRPQS(v)) and minimal resolvable coverings of triples by quadruples of order v (MRCQS(v)). We show that an MRPQS(v) (MRCQS(v)) with the number of blocks meeting the upper (lower) bound exists if and only if v≡0 (mod 4). As a byproduct, we also show that a uniformly resolvable Steiner system URS(3, {4, 6}, {r₄, r₆}, v) with r₆≤1 exists if and only if v≡0 (mod 4). All of these results are obtained by the approach of establishing a new existence result on RH(6²ⁿ) for all n≥2. © 2009 Wiley Periodicals, Inc. J Combin Designs 18: 209–223, 2010     

Quantum double constructions for compact quantum group

For a non-degenerate pair of compact quantum groups, we first construct the quantum double as an algebraic compact quantum group in an algebraic framework. Then by adopting some completion procedure, we give the universal and reduced quantum double constructions in the correspondence C＊-algebraic settings, which generalize Drinfeld＇s quantum double construction and yield new C＊-algebraic compact quantum groups.