动态环境约束下企业的资本积累

本文讨论动态环境约束下企业的动态投资行为,拓广了文献[4]的结果.为了使讨论的问题更符合实际情况,本文假设政府设定的污染排放上限是与企业的规模大小有关,即假设污染排放上限是生产资本的函数,讨论动态环境约束下企业的最佳动态投资行为,并为政府制定污染排放政策提供依据.     

氨基乙硫醇修饰金电极直接测定芦丁含量的研究

利用分子自组装技术制备氨基乙硫醇修饰金电极,并采用脉冲伏安法直接测定芦丁的含量。以pH7.0的乙醇和磷酸盐混合缓冲溶液作底液,芦丁在氨基乙硫醇修饰金电极上于0.19 V(vs.SCE)处呈现一灵敏的氧化电流峰,峰电流和芦丁的浓度在8.0~2.5×102μmol/L范围内呈良好的线性关系。由于抗坏血酸在氨基乙硫醇修饰金电极上的氧化电位出现显著负移,因此,可避免抗坏血酸对芦丁检测的干扰。本方法可以不经预分离直接检测药物中芦丁含量。     

共振光散射法研究脱氧核糖核酸与多胺的相互作用及精胺的测定

在一定条件下,精胺不仅能够与脱氧核糖核酸(DNA)大沟嵌入结合,还能与DNA链上的碱基和磷酸基进行链内结合和跨链结合,形成致密的环状螺旋结构,造成DNA的凝聚,从而使DNA共振光散射(RLS)强度强烈地增强。增强的共振光散射强度与精胺的浓度呈现良好的线性关系,线性范围为5.0×10-7~1.0×10-5mol/L;校正曲线的回归方程为IRLS=40.22 5.28×107C(mol/L),相关系数r=0.9936;检出限(3σ)为7.4×10-8mol/L。在测定精胺的线性范围内,其它多胺(亚精胺,腐胺)、蛋白质及常见的金属离子不干扰测定。该方法用于测定新几内亚凤仙中的精胺,获得满意结果。     

Ring-opening metathesis copolymerization employing ruthenium-based metathesis catalysts

The copolymerization of both high- and low-strain cyclic olefins employing three ruthenium-based metathesis catalysts is desribed. The effect of the ligand environment as well as the nature of the carbene on the copolymerizations is discussed.     

不同溶剂中番茄红素的荧光光谱及其特性研究

用970CRT荧光光度计测定了番茄红素在正己烷、乙酸乙酯、四氢呋喃、氯仿、丙酮和苯等6种溶剂中的荧光光谱以及番茄红素在四氢呋喃溶液中不同浓度下的荧光光谱。对所测光谱分析得出:6种溶剂中荧光光谱的最大峰值波长(λmax)分别为542.5 nm5、48.2 nm5、55.0 nm、555.7 nm、556.4 nm和565.7 nm,由于溶剂效应,随溶剂极性由小到大,荧光光谱的最大峰值波长(λmax)逐渐红移,由这些峰值波长计算得出相应的番茄红素分子在6种溶剂中的跃迁能ET分别为220.5 kJ/mol2、18.2 kJ/mol2、15.6 kJ/mol2、15.3 kJ/mol2、14.9 kJ/mol和211.5 kJ/mol,可见跃迁能ET也随溶剂极性增大而降低;当番茄红素在四氢呋喃溶液中的质量浓度低于50μg/ml时,溶液的荧光强度随溶液浓度增加而增大,当质量浓度高于50μg/ml时,由于番茄红素的激发态分子与基态分子相互作用,荧光强度反而减小;在浓度低于80μg/ml的溶液中,番茄红素的荧光光谱除最大峰值外还有三个较小峰值,据此计算得出相应的番茄红素分子的跃迁能分别为E(T1)=278.2 kJ/mol、E(T2)=260.2 kJ/mol和E(T3)=239.3 kJ/mol。     

280mm×280mm口径单脉冲过程电光开关

用于高功率惯性约束聚变(ICF)激光驱动器的大口径电光开关均采用等离子体电极泡克耳斯盒。与传统的等离子体电极电光开关原理不同,单脉冲过程驱动电光开关没有独立的大电流等离子体发生单元,而只是通过具有较高幅值的正负开关脉冲完成对大口径电光开关的驱动。介绍单脉冲过程驱动等离子体电极泡克耳斯盒电光开关的设计,并建立280 mm×280 mm口径电光开关实验平台,利用连续激光器测试了电光开关特性,实验测得该电光开关中心处开关效率为99.3%,开关上升时间为90 ns。     

脉冲压缩光栅光路调节新方法研究

介绍了一种简单而实用的大口径脉冲压缩光栅光路调节方法,有效解决了普通光路调节方法中轴向调节精度不高的问题。首先由全息透镜(光栅)成像公式出发,推导出了该光路调节的基本原理。并从光栅记录系统与光栅衍射波像差的关系,结合初级像差理论推导得出叠栅条纹像差为0.4786λ,大约是光栅衍射波像差(0.25λ)的两倍,利用此关系也可对光栅衍射波像差进行实时监测。从数值模拟结果可知,利用叠栅条纹法调节光路可将光栅波像差减至0.06λ,相应的轴向误差量为0.007 mm,可有效提高了轴向调节精度。     

Highly effective and chemoselective hydrodeoxygenation of aromatic alcohols

Effective hydrodeoxygenation (HDO) of aromatic alcohols is very attractive in both conventional organic synthesis and upgrading of biomass-derived molecules, but the selectivity of this reaction is usually low because of the competitive hydrogenation of the unsaturated aromatic ring and the hydroxyl group. The high activity of noble metal-based catalysts often leads to undesired side reactions (e.g., saturation of the aromatic ring) and excessive hydrogen consumption. Non-noble metal-based catalysts suffer from unsatisfied activity and selectivity and often require harsh reaction conditions. Herein, for the first time, we report chemoselective HDO of various aromatic alcohols with excellent selectivity, using porous carbon–nitrogen hybrid material-supported Co catalysts. The C–OH bonds were selectively cleaved while leaving the aromatic moiety intact, and in most cases the yields of targeted compounds reached above 99% and the catalyst could be readily recycled. Nitrogen doping on the carbon skeleton of the catalyst support (C–N matrix) significantly improved the yield of the targeted product. The presence of large pores and a high surface area also improved the catalyst efficiency. This work opens the way for efficient and selective HDO reactions of aromatic alcohols using non-noble metal catalysts.

Porous carbon–nitrogen hybrid material-supported Co catalysts can effectively promote the chemoselective hydrodeoxygenation reaction of a various of aromatic alcohols in ethanol and hydrogen atmosphere, under relatively mild conditions.     

Upper Bound Shakedown Analysis of Plates Utilizing the C1 Natural Element Method

This paper proposes a numerical solution method for upper bound shakedown analysis of perfectly elasto-plastic thin plates by employing the C1 natural element m...