三参数Weibull分布下随机截尾恒加寿命试验的Bayes统计分析

利用随机截尾恒加寿命试验所获的数据，导出了三参数Ｗｅｉｂｕｌ分布在平方损失下，三个参数的Ｂａｙｅｓ估计，进一步估计了在正常应力水平下的各种可靠性指标     

加强工科院校人文素质教育的思考

加强工科院校人文素质教育势在必行，为此，必须确立专业科技教育与人文素质教育并重的教育思想，重视人文素质教育，努力探索，并构建符合本校实际的人文素质教育的模式。     

块对称加速超松弛迭代法及其收敛性

给出了解线性代数方程组Ａｘ＝ｂ的一个新的迭代算法模型——块对称加速超松弛迭代法（ＢＳＡＯＲ迭代法），并在系数矩阵Ａ为块Ｈ－矩阵的条件下，证明了该模型的收敛性．在该模型中，对参数取特殊值可得到块对称Ｇａｕｓｓ－Ｓｅｉｄｅｌ迭代法和块对称ＳＯＲ迭代法等常用的块对称迭代算法，并且还可产生许多新的块对称迭代法．即事实上建立了块对称迭代法的一般性收敛理论．     

The strong cooperativity of dioxygen binding by dicobalt (II) diporphyrin compounds in nonaqueous solution at room temperature

Thermodynamic data were determined for the reversible binding of O₂ to two compounds of dicobalt(II) di(meso-tetra-phenyl)porphyrin derivatives with different lengths of diamidoaliphatic bridge (abbreviated to Co₂PP₈ and Co₂PP₄) in N,N-dimethylformamide at room temperature. The partial pressure of dioxygen necessary for half-oxygenation (P _1/2) and hill coefficient (n) at 298 K were determined as follows:P _1/2=54.2 kPa,n=2.0 for Co₂PP₈ andP _1/2=6.8 kPa,n=1.8 for Co₂PP₄, respectively. The rate equations of reversible oxygen binding by Co₂PP₈ were determined and the reaction path was proposed. The results of ther-modynamic and kinetic studies indicate that there exists strong cooperative effect during oxygenation of the compounds. The ESR observation reveals that the dioxygen complexes formed in the solutions are of superoxo (Co-O ₂ ⁻ ) type. Supported by the Research Foundation of the State Education Commission of China Zhou Xiaohai: born in 1962, Ph.D. Associate professor     

Studies on the reaction between Laccase ando-methoxyphenol by microcalorimetry

The reaction between Laccase ando-methoxyphenol have been studied by LKB-2107 batch microcalorimetry system. Thermodynamic parameters Δ _r H _m , ΔG _o , ΔG _T ^≠ and kinetic parameters (K _m ,k ₂) have been determined. The process of the reaction has been analyzed from changes in energy by using the transition state theory. Two methods for enhancing catalytic power of Laccase are proposed. The results shown that formation of an enzyme-substrate complex is “anticatalytic”. The enter and sole source of catalytic power is the stabilization of transition state; reactant-state interactions are by nature inhibitory and only waste catalytic power. Supported by the National Natural Science Foundation of China Wang Tianzhi: born in 1968. Ph D