诃子与川楝子配伍后挥发油化学成分分析

采用水蒸气蒸馏法将诃子与川楝子按1∶1的质量比配伍后提取挥发油,并用GC-M S联机技术对其化学成分进行研究,分离出249个组分,鉴定了其中的13个,主要成分有单[2-乙基己基]邻苯二甲酸、2,2′-亚甲基叔丁基对甲酚,乙基（2E）-3-[4-甲氧基苯基]-2-丙烯、7-甲基-Z-十四烯-1-醇酯。     

地声参数及传播损失不确定性估计与建模

地声参数的不确定性对水声传播具有重要的影响。通过贝叶斯理论建立水声环境不确定性推理模型,理论推导了地声参数的似然函数以及地声参数和传播损失的后验概率密度,并采用MCMC(Markov Chain Monte Carlo)进行了仿真计算,给出了地声参数的二维后验联合概率密度和一维边缘概率密度,在此基础上对传播损失的不确定性进行了估计,得到了传播损失80%的可信区间。仿真和实验结果表明,该方法适用于地声参数反演和不确定性估计,并能获取因地声参数不确定性导致的传播损失不确定性估计。     

大离轴量凹面取样镜的设计

根据系统的使用要求以及椭球面特有的成像性质,提出使用离轴椭球面来完成光束取样和完善成像的设计方式.利用设计输入,计算出镜面的初始结构参数,得到离轴椭球面的二次曲线方程,将计算结果带入光学设计软件ZEMAX中验证成像质量.结果表明:离轴椭球面不但将物点和像点分开,减小了系统的长度,而且在像点处成完善像,将离轴成像转换为轴上成像,使后续光斑成像系统的高质量成像易于实现.     

Stability of convective patterns in reaction fronts: a comparison of three models

Autocatalytic reaction fronts generate density gradients that may lead to convection. Fronts propagating in vertical tubes can be flat, axisymmetric, or nonaxisymmetric, depending on the diameter of the tube. In this paper, we study the transitions to convection as well as the stability of different types of fronts. We analyze the stability of the convective reaction fronts using three different models for front propagation. We use a model based on a reaction-diffusion-advection equation coupled to the Navier-Stokes equations to account for fluid flow. A second model replaces the reaction-diffusion equation with a thin front approximation where the front speed depends on the front curvature. We also introduce a new low-dimensional model based on a finite mode truncation. This model allows a complete analysis of all stable and unstable fronts.     

Thermolysis of 3‐alkyl‐3‐methyl‐1,2‐dioxetanes: Activation parameters and chemiexcitation yields

3‐Methyl‐3‐(3‐pentyl)‐1,2‐dioxetane 1 and 3‐methyl‐3‐(2,2‐dimethyl‐1‐propyl)‐1,2‐dioxetane 2 were synthesized in low yield by the α‐bromohydroperoxide method. The activation parameters were determined by the chemiluminescence method (for 1 ΔH‡ = 25.0 ± 0.3 kcal/mol, ΔS‡ = −1.0 entropy unit (e.u.), ΔG‡ = 25.3 kcal/mol, k₁ (60°C) = 4.6 × 10⁻⁴s⁻¹; for 2 ΔH‡ = 24.2 ± 0.2 kcal/mol, ΔS‡ = −2.0 e.u., ΔG‡ = 24.9 kcal/mol, k₁ (60°C) = 9.2 × 10⁻⁴s⁻¹. Thermolysis of 1–2 produced excited carbonyl fragments (direct production of high yields of triplets relative to excited singlets) (chemiexcitation yields for 1: ϕ^T = 0.02, ϕ ≤ 0.0005; for 2: ϕ^T = 0.02, ϕ^S ≤ 0.0004). The results are discussed in relation to a diradical‐like mechanism. © 2001 John Wiley & Sons, Inc. Heteroatom Chem 12:459–462, 2001     

铪元素及其同位素的发现：技术进步和思想发展的共同结晶

1869年，门捷列夫在第一张元素周期表中的锆元素后留出原子量为180的元素位置，预测铪与锆同族。1913年，原子序数和莫斯莱定律的提出揭示了铪元素在周期表中位置排列的实质，为铪元素的发现提供理论基础。20世纪20年代，玻尔理论的发展证实铪与锆同族，指导科学家从锆矿石中寻找铪元素。1923年，赫维西和科斯特借助X射线光谱技术发现铪元素，彰显了X射线光谱技术的独特价值。20世纪30年代以后，同位素理论和质谱技术促成了铪同位素的发现，使人们对铪元素有了新的认识。总之，铪元素及其同位素的发现是技术进步和思想发展的共同结晶。