轮图的广义Mycielski图的邻强边色数

设图 G(V,E)为简单图 ,V(Mn(G) ) |{ v0 1,v0 2 ,… ,v0 p;v11,v12 ,… ,v1p,… ,vn1,vn2 ,… ,vnp}E(Mn(G) ) =E(G)∪ { vijv(i+ 1) k|v0 jv0 k ∈ E(G) ,1≤ j,k≤ p ,i =0 ,1,… ,n - 1}称 Mn(G)为 G的 n广义 Mycielski图 ,n为自然数 .本文得到了轮的广义 Mycielski图的临强边色数 .     

三维内肋管内插入螺旋扭带的强化传热实验

本文分别以水和乙二醇为工质，在Ｒｅ数范围为：６００～４００００，Ｐｒ数范围为：５．５～１１０之间，对四根分别插入三种不同扭率螺旋扭带的三维内助管内的换热和流阻特性进行了实验研究。结果表明：三维内肋管内加装扭带的强化传热技术适用于低Ｒｅ数下高Ｐｒ数工质的管内对流换热强化。根据实验值得到了流阻和换热关联式。     

Large deviations for heavy-tailed random sums of independent random variables with dominatedly varying tails

We prove large deviation results on the partial and random sums Sn = ∑i=1n Xi,n≥1; S(t) = ∑i=1N(t) Xi, t≥0, where {N(t);t≥0} are non-negative integer-valued random variables and {Xn;n≥1} are independent non-negative random variables with distribution, Fn, of Xn, independent of {N(t); t≥0}. Special attention is paid to the distribution of dominated variation.     

Soliton molecules and the CRE method in the extended mKdV equation

The soliton molecules of the(1+1)-dimensional extended modified Korteweg–de Vries(mKdV)system are obtained by a new resonance condition, which is called velocity resonance. One soliton molecule and interaction between a soliton molecule and one-soliton are displayed by selecting suitable parameters. The soliton molecules including the bright and bright soliton, the dark and bright soliton, and the dark and dark soliton are exhibited in figures 1–3, respectively.Meanwhile, the nonlocal symmetry of the extended mKdV equation is derived by the truncated Painlevé method. The consistent Riccati expansion(CRE) method is applied to the extended mKdV equation. It demonstrates that the extended mKdV equation is a CRE solvable system. A nonauto-B?cklund theorem and interaction between one-soliton and cnoidal waves are generated by the CRE method.     

G波段500 W带状注扩展互作用速调管设计研究

针对太赫兹频段实现高功率面临物理机制上的难题,设计了一个G波段带状注速调管,展示了基于非相对论带状电子注和扩展互作用技术所能达到的功率水平以及影响性能的物理因素。文中设计基于电压24.5 kV、电流0.6 A,1 mm×0.15 mm的椭圆电子注,以及与之相匹配的互作用系统,即横向过尺寸哑铃型多间隙谐振腔,可以实现高功率和高增益。三维PIC仿真结果显示,在考虑实际腔体损耗的情况下,能够获得超过500 W的功率,电子效率和增益分别达到3.65%和38.2 dB。研究发现,输出功率和效率的提升很大程度上受到多间隙腔模式稳定性以及电路欧姆损耗的制约;输出腔的欧姆损耗对输出功率影响尤为显著,工程设计需要特别考虑。本文的研究为高频段带状注扩展互作用器件的研发打下了良好的基础。     

扩展幂律型脱钉和高温超导体及MgB2的电阻转变

近来，关于无序涡旋物质凝聚体的著名的涡旋玻璃理论受到了来自某些新实验的严重质疑．我们重新审查了高温超导体的临界标度，发现超导混合态的直流伏安特性具有扩展幂律的一般形式．由该扩展幂律型非线性方程模拟的等温线和Strachan等人得到的实验数据[Phys．Rev．Lett．87（2001），067007]符合得很好．文中还讨论了长期以来围绕纵向电阻率和霍尔电阻率的临界指数的某些争议．     

Extended Bose-Hubbard model with pair hopping on triangular lattice

We study systematically an extended Bose-Hubbard model on the triangular lattice by means of a meanfield method based on the Gutzwiller ansatz. Pair hopping terms are explicitly included and a three-body constraint is applied. The zero-temperature phase diagram and a variety of quantum phase transitions are investigated in great detail. In particular, we show the existence and the stability of the pair supersolid phase.     

Extended X‐ray absorption fine structure and multiple‐scattering simulation of nickel dithiolene complexes Ni[S2C2(CF3)2]2n (n = −2, −1, 0) and an olefin adduct Ni[S2C2(CF3)2]2(1‐hexene)

A series of Ni dithiolene complexes Ni[S₂C₂(CF₃)]₂ⁿ (n = ?2, ?1, 0) ( 1 , 2 , 3 ) and a 1‐hexene adduct Ni[S₂C₂(CF₃)₂]₂(C₆H₁₂) ( 4 ) have been examined by Ni K‐edge X‐ray absorption near‐edge structure (XANES) and extended X‐ray absorption fine‐structure (EXAFS) spectroscopies. Ni XANES for 1 – 3 reveals clear pre‐edge features and approximately +0.7 eV shift in the Ni K‐edge position for `one‐electron' oxidation. EXAFS simulation shows that the Ni—S bond distances for 1 , 2 and 3 (2.11–2.16 Å) are within the typical values for square planar complexes and decrease by ～0.022 Å for each `one‐electron' oxidation. The changes in Ni K‐edge energy positions and Ni—S distances are consistent with the `non‐innocent' character of the dithiolene ligand. The Ni—C interactions at ～3.0 Å are analyzed and the multiple‐scattering parameters are also determined, leading to a better simulation for the overall EXAFS spectra. The 1‐hexene adduct 4 presents no pre‐edge feature, and its Ni K‐edge position shifts by ?0.8 eV in comparison with its starting dithiolene complex 3 . Consistently, EXAFS also showed that the Ni—S distances in 4 elongate by ～0.046 Å in comparison with 3 . The evidence confirms that the neutral complex is `reduced' upon addition of olefin, presumably by olefin donating the π‐electron density to the LUMO of 3 as suggested by UV/visible spectroscopy in the literature.     

Tris‐amidoximate uranyl complexes via η2 binding mode coordinated in aqueous solution shown by X‐ray absorption spectroscopy and density functional theory methods

The present study sheds some light on the long‐standing debate concerning the coordination properties between uranyl ions and the amidoxime ligand, which is a key ingredient for achieving efficient extraction of uranium. Using X‐ray absorption fine structure combined with theoretical simulation methods, the binding mode and bonding nature of a uranyl–amidoxime complex in aqueous solution were determined for the first time. The results show that in a highly concentrated amidoxime solution the preferred binding mode between UO₂²⁺ and the amidoxime ligand is η² coordination with tris‐amidoximate species. In such a uranyl–amidoximate complex with η² binding motif, strong covalent interaction and orbital hybridization between U 5f/6d and (N, O) 2p should be responsible for the excellent binding ability of the amidoximate ligand to uranyl. The study was performed directly in aqueous solution to avoid the possible binding mode differences caused by crystallization of a single‐crystal sample. This work also is an example of the simultaneous study of local structure and electronic structure in solution systems using combined diagnostic tools.     

An analysis of the radiation reaction in a charged dumbbell

We make a thorough non-covariant analysis of the derivation of the equation of motion for a charged particle, including radiation reaction, by means of a simple model for the charge: a dumbbell. This model and our method to expand retarded quantities, based on complex-variable theory, allow us to avoid some of the usual approximations, so we can show several features of the radiation reaction problem.