Numerical Simulation of Solitary Kinetic Alfvén Waves

Using the two-fluid model in the case of α〉〉1 （α= β/2Q, β is the ratio of thermal pressure to magnetic pressure, and Q = me/mi ）, we numerically investigate the interactions between two solitary kinetic Alfvén waves （SKAWs） and between an SKAW and a density discontinuity. The results show that the two SKAWs would remain in their original shapes and propagate at their initiating speeds, which indicates that SKAWs behave just like standard solitons. The simulation also shows that SKAWs will reflect and refract when crossing a discontinuity and propagating into a higher density region. The transmission wave is an SKAW with increasing density, and the reverberation is a disturbance with lower amplitude.     

用户需求行为对互联网动力学整体特性的影响

由Internet构成的复杂网络的动力学特性主要受到用户需求行为的影响,具备时域的统计规律性. 通过对区域群体用户需求行为的时域实验统计分析,发现用户对Web网站的访问频度及其生成的二分网络的入度分布也呈现幂律分布和集聚现象,其幂指数介于1.7到1.8之间. 建立了虚拟资源网络VRN和物理拓扑网络PTN双层模型,分析了双层模型映射机理,并对网络用户需求行为进行建模. 虚拟资源网络VRN对物理拓扑网络PTN映射过程的不同机理,模拟了Internet资源网络到物理网络的不同影响模式. 幂律分布的用户需求特性会 关键词： 复杂网络 无标度拓扑 用户需求 相变     

全血中维生素E和辅酶Q10含量的高效液相色谱法测定

建立了一种同时测定全血中维生素E和辅酶Q10的高效液相色谱法.样品经乙醇沉淀蛋白,以正己烷萃取,氮气吹干后,流动相溶解,以甲醇-乙醇(体积比20 : 80)为流动相,在C18柱 (5 μm, 250 mm×4.6 mm i.d.)上进行色谱测定.维生素E和辅酶Q10的线性范围皆为1.0 ～50.0 mg/L,检出限分别为0.21、0.15 mg/L,相对标准偏差分别为5.2%、5.9%;全血样品的维生素E和辅酶Q10加标回收率分别为97%～115%和90%～112%.     

The Initial Reactions of H3PO4 and NaH2PO4Supported on Silica: A Joint Experimental and Theoretical Study

利用XRD、TG、DRIFTS、31P MAS NMR和密度泛函理论研究了浸渍法制备的硅胶负载型磷酸和磷酸二氢钠催化剂,阐明了催化剂制备过程中生成的初始缩合产物和其反应机理. 光谱试验结果显示,在二氧化硅负载的磷酸上,除了聚磷酸外,还有硅磷酸盐的存在;在二氧化硅负载的磷酸二氢钠上,仅发现聚磷酸钠存在. 密度泛函模拟结果也证明,磷酸与二氧化硅表面硅羟基之间的反应在缩合反应的初始阶段比其自身的二聚反应更为有利. 但是在硅胶负载的磷酸二氢钠上,磷酸二氢钠的二聚和三聚是缩合反应初始阶段的主要反应.     

微型滴定法测定硫酸亚铁的含量

将微型滴定用于硫酸亚铁含量的测定 ,设计并使用与微型滴定管精度一致的移液管 ,比较了微型滴定与常量滴定的测定结果。方法可行 ,有使用价值。     

Poisson–Dirichlet distribution with small mutation rate

A large deviation principle is established for the Poisson–Dirichlet distribution when the mutation rate θ$\theta$ converges to zero. The rate function is identified explicitly, and takes on finite values only on states that have finite number of alleles. This result is then applied to the study of the asymptotic behavior of the homozygosity, and the Poisson–Dirichlet distribution with selection. The latter shows that several alleles can coexist when selection intensity goes to infinity in a particular way as θ$\theta$ approaches zero.     

The facile in situ preparation and characterization of C/FeOF/FeF<Subscript>3</Subscript> nanocomposites as LIB cathode materials

C/FeOF/FeF₃ nanocomposite was synthesized by a facile in situ partial oxidation method. High-resolution transmission electron microscopy (HR-TEM) showed a special texture comprised of interpenetrating nanodomains of FeOF and FeF₃. Cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) measurements revealed that the introduction of nanodomain FeOF enhanced both the electronic and ionic conductivity of the composite material. Therefore, the improvement of electron and lithium-ion dynamics resulted in the significant enhancement of the electrochemical performances of the material at ambient temperature. At a current density of 20 mA g^?1 within potential range 1.5–4.5 V, the specific capacities of the first ten circles were maintained at about 400 mAh g^?1 _. This material also exhibited excellent cycling capacity retention capability especially for high C rates. When the current density further increased to 100 and 200 mA g^?1, a steady capacity of 80 and 60 mAh g^?1 was observed, respectively. Furthermore, nearly no capacity loss was observed for the followed cycles. The discharge platforms based on intercalation and conversion reaction were also heightened by about 0.4 V, which increased the contribution of high voltage capacities. Compared to C/FeF₃, C/FeOF/FeF₃ is showing more of capacitive behavior, which also contributes to the high specific capacity delivered and is believed to be closely related to the enlarged nanodomain interfaces between two electrochemical active materials. An expansion-cracking-oxidation mechanism was proposed to explain the formation of this interpenetrating nanodomains of FeOF and FeF₃.