微加工薄膜变形镜特性分析

 借助测量微加工薄膜变形镜驱动器的面形影响函数，分析了驱动器的电压-位移函数和驱动器之间的线性叠加性;通过对连续面形变形镜拟合像差的理论分析和实验研究，建立了微加工薄膜变形镜电压解耦模型。分析了对前36阶Zernike模式的拟合残差和拟合能力，指出微加工薄膜变形镜仅可用来拟合低级像差并且有较大的拟合能力和较小的拟合残差，而不能拟合高级像差。     

变频压缩机空调系统的理论分析及实验研究

变频空调器是由变频压缩机驱动的空调系统,压缩机通过变频调节其转速使压缩机单位时间内的排气量变化,从而达到调节制冷量的目的。本文提出了变频空调器制冷系统的原理和设计方法,具体给出了制冷量和压缩机频率的关系方程,并从理论和实验两方面对变频空调器制冷系统进行了分析,得到了频率曲线图,为变频空调器制冷系统的设计提供了依据。     

Lemniscates and inequalities for the logarithmic capacities of continua

It is shown that if P(z) = z ⁿ + ? is a polynomial with connected lemniscate E(P) = {z: ¦P(z)¦ ≤ 1} and m critical points, then, for any n? m+1 points on the lemniscate E(P), there exists a continuum γ ? E(P) of logarithmic capacity cap γ ≤ 2^?1/n which contains these points and all zeros and critical points of the polynomial. As corollaries, estimates for continua of minimum capacity containing given points are obtained.     

Finite turns and the regular closure of linear context-free languages

Turn bounded pushdown automata with different conditions for beginning a new turn are investigated. Their relationships with closures of the linear context-free languages under regular operations are studied. For example, automata with an unbounded number of turns that have to empty their pushdown store up to the initial symbol in order to start a new turn are characterized by the regular closure of the linear languages. Automata that additionally have to re-enter the initial state are (almost) characterized by the Kleene star closure of the linear languages. For both a bounded and an unbounded number of turns, requiring to empty the pushdown store is a strictly stronger condition than requiring to re-enter the initial state. Several new language families are obtained which form a double-stranded hierarchy. Closure properties of these families under AFL operations are derived. The regular closure of the linear languages share the strong closure properties of the context-free languages, i.e., the family is a full AFL. Interestingly, three natural new language families are not closed under intersection with regular languages and inverse homomorphism. Finally, an algorithm is presented parsing languages from the new families in quadratic time.     

一种自制的蒸馏水器保护装置

本装置由检测、控制、执行、报警和电源五部分组成。检测部分采用了靠正常水位导通的两根信号线。当蒸馏水器在正常运行时遇停水,本装置可立即实现断电保护,同时发出声光报警,有效防止干烧,杜绝事故发生。本装置制作简便,元器件均为市售,成本低廉,性能可靠。     

LiCoO2中锂离子固相扩散系数随循环次数的变化

The solid diffusion coefficient of lithium-ion in LiCoO₂ cathode material has been investigated by the capacity intermittent titration technique (CITT) at different voltages and at different charge/discharge cycles. By SEM, XRD and FTIR techniques, the structure of LiCoO₂ was studied before and after charge-discharge cycles, and the relationship between solid diffusion coefficient and crystal structure was further discussed. CITT results show that the value of Li⁺ solid diffusion coefficient of LiCoO₂ is about 10^-12 cm²·s^-1. During the whole charge-discharge cycles, the Li⁺ solid diffusion coefficient decreased within the voltage of 4.0～4.3 V, which is attributed to the change of the structure of LiCoO₂.     

Dimerization of some substituted benzoic acids in aqueous solution from conductance measurements

Precision molar conductances of benzoic, o-toluic, 2,6-dimethylbenzoic, 2,3,6-trimethylbenzoic, and, o-fluorobenzoic acids have been determined in aqueous solution as a function of temperature and of concentration up to near saturation (<0.035 M). At the higher concentrations molar conductances are found to be less than anticipated for the simple dissociation of a 1-1 electrolyte. Although the deviations are only 1% or less they have been interpreted to show that these acids are dimerized in solution. The interpretation includes an assumption that the dimer ionizes to produce a triple ion. Increasing numbers of methyl groups lead to increasing dimerization. For those acids with two ortho groups the dimerization increases with increasing temperature while the other three show decreasing dimerization with increasing temperature. Temperature functions have been determined for the dimerization constants and from these functions standard changes in enthalpy, entropy, and heat capacity have been determined. Comparisons are made with dimerization studies in non-aqueous solvents. From these as well as the behavior of benzene in water it is concluded that a major factor driving the dimerization is hydrophobic interaction. To provide a limiting conductance of the triple ion needed in the dimerization calculations a conductance study was also made for o-Phenylbenzoic acid on the assumption that its anion provides an approximate model of the triple ion.     

Schiff碱配合物的研究：Ⅶ.硅胶表面Schiff碱的配位作用

有机高分子Schiff碱对金属离子的螯合作用已引起人们的兴趣。硅胶为无定形高比表面无机高分子,通过氯甲基化,可进行多种化学反应而形成各种表面基团。本文报道四种新型硅胶表面Schiff碱(图1),考察了它们对Cu~(2 ),Co~(2 ),Cd~(2 )和Pb~(2 )的配位作用。     

Microheterogeneity in aqueous-organic solutions: Heat capacities,volumes and expansibilities of some alcohols,aminoalcohol and tertiary amines in water

The heat capacities per unit volume and the densities of aqueous solutions of 2-propanol, neopentanol, tert-amylalcohol, 2-amino-2-methylpropanol, triethylamine and diethylmethylamine were measured, in many cases as a function of temperature, over the whole mole fraction or solubility range. Apparent and partial molal heat capacities, volumes and expansibilities were derived. The concentration dependence of these functions suggest the existence of transitions in some of these systems, in the water-rich region, qualitatively similar to micellization. The large relaxation contribution observed with some of the thermodynamic functions of hydrophobic alcohols and amines suggests a reinforcement of hydrophobic hydration due to strong hydrogen-bonding interactions of the polar groups with water.     

Thermodynamic properties of organic compounds in aqueous solution. II. Apparent molal heat capacities of piperidines,morpholines, and piperazines

Apparent molal heat capacities of some piperidine, morpholine, and piperazine derivatives in aqueous solution have been determined by adiabatic calorimetry in the temperature range 20–55°C and in the molality range 0.2–1m. Comparison of experimental values with those calculated through group contributions, found for monofunctional compounds, indicates strong interactions between the hydrophilic centers. An interpretation is given of the possible mechanism of this interaction. Also, values of ΔC _p for the addition reaction of proton to nitrogen centers of mono- and bifunctional organic compounds are examined.