用于Z箍缩X辐射谱诊断的柱面凸晶摄谱仪的性能分析

 考虑X光源的空间尺寸和晶体的摇摆曲线,用光线追迹方法计算了诊断丝阵Z箍缩等离子体X辐射谱的柱面凸晶摄谱仪的色散、能谱分辨和空间分辨以及系统参数对它们的影响。结果表明：决定柱面凸晶摄谱仪能谱分辨的主要因素是光源尺寸以及光源-晶体之间距离;增大光源-晶体之间距离能够改善能谱分辨,但导致径向空间分辨能力下降。并依此建立了云母晶体摄谱仪,在“强光一号”装置上对系统进行了测试,获得时间积分铝丝阵负载Z箍缩等离子体X辐射谱。     

空中目标多波段红外辐射特性描述与仿真分析

针对空中目标在复杂背景下的探测需求,根据实际目标的运动特性,分析目标在飞行高度、飞行姿态角改变时的辐射特点,基于MODTRAN计算得到大气辐射和衰减数据,建立目标的三维模型、热辐射和反射模型,搭建空中目标的红外成像仿真系统.分析和仿真结果表明:在中波波段,目标尾焰的红外辐射比蒙皮强很多,在长波波段,蒙皮的红外辐射比较强,仿真图像的细节比较多,尾焰的红外辐射虽然有所减弱,红外成像效果依旧很好;相同探测条件下,由于位置越高大气越稀薄,探测器的可探测距离会变得比较远.目标红外辐射特性的分析和红外仿真系统的搭建对缩短红外探测器的研制周期和进一步确定探测器波段和系统分辨率等指标提供了参考依据.     

An efficient algorithm for the three-guard problem

Given a simple polygon P with two vertices u and v, the three-guard problem asks whether three guards can move from u to v such that the first and third guards are separately on two boundary chains of P from u to v and the second guard is always kept to be visible from two other guards inside P. It is a generalization of the well-known two-guard problem, in which two guards move on the boundary chains from u to v and are always kept to be mutually visible. In this paper, we introduce the concept of link-2-ray shots, which can be considered as ray shots under the notion of link-2-visibility. Then, we show a one-to-one correspondence between the structure of the restrictions placed on the motion of two guards and the one placed on the motion of three guards, and generalize the solution for the two-guard problem to that for the three-guard problem. We can decide whether there exists a solution for the three-guard problem in O(nlogn) time, and if so generate a walk in O(nlogn+m) time, where n denotes the number of vertices of P and the size of the optimal walk. This improves upon the previous time bounds O(n²) and O(n²logn), respectively. Moreover, our results can be used to solve other more sophisticated geometric problems.     

Ray shooting and intersection searching amidst fat convex polyhedra in 3-space

We present a data structure for ray-shooting queries in a set of convex fat polyhedra of total complexity n in . The data structure uses O(n^2+ε) storage and preprocessing time, and queries can be answered in O(log²n) time. A trade-off between storage and query time is also possible: for any m with n<m<n², we can construct a structure that uses O(m^1+ε) storage and preprocessing time such that queries take time.We also describe a data structure for simplex intersection queries in a set of n convex fat constant-complexity polyhedra in . For any m with n<m<n³, we can construct a structure that uses O(m^1+ε) storage and preprocessing time such that all polyhedra intersecting a query simplex can be reported in O((n/m^1/3)logn+k) time, where k is the number of answers.     

Photocycloaddition Reactions of 5,5‐Dimethyl‐3‐(3‐methylbut‐3‐en‐1‐ynyl)cyclohex‐2‐en‐1‐one

The title cyclohexenone 1d undergoes photodimerization selectively at the exocyclic C?C bond to give a 1 : 1 mixture of 1,2‐dialkynyl‐1,2‐dimethylcyclobutanes 6 and 7 . On irradiation in the presence of 2,3‐dimethylbuta‐1,3‐diene, 1d affords bicyclo[8.4.0]tetradeca‐1,2,3,7‐tetraen‐11‐one 9 . This – formal – (6+4)‐cycloadduct undergoes quantitative isomerization to 3‐cycloheptadienyl‐2,5,5‐trimethylcyclohex‐2‐enone 11 on treatment with basic silica gel.     

Addition Reactions of Sulfenyl and Sulfinyl Chlorides with 3‐Phenyl‐1‐azabicyclo[1.1.0]butane

The reactions of 3‐phenyl‐1‐azabicyclo[1.1.0]butane with α‐chlorosulfenyl chlorides and sulfinyl chlorides lead to the corresponding sulfenamides and sulfinamides, respectively, which possess an azetidine ring. It is proposed that a two‐step mechanism occurs involving an intermediate carbenium ion, which is formed by the addition of the electrophile at the N‐atom and cleavage of the N(1)? C(3) bond. The structures of 9b and 10b are established by X‐ray crystallography.     

Nortriterpenoids from Schisandra wilsoniana

Three new highly oxygenated nortriterpenoids, wilsonianadilactones A–C ( 1 – 3 ), together with twelve known ones, i.e., 4 – 15 , were isolated from the leaves and stems of Schisandra wilsoniana. Their structures were established by means of extensive analysis of spectroscopic data, and compound 1 was further confirmed by X‐ray crystallographic diffraction. Compounds 1 – 3 showed weak anti‐HIV‐1 activity with EC₅₀ values of 23.5, 55.5, and 66.4 μg/ml, respectively.     

Urinary exposure marker discovery for toxicants using ultra-high pressure liquid chromatography coupled with Orbitrap high resolution mass spectrometry and three untargeted metabolomics approaches

Human biomonitoring is the assessment of actual internal contamination of chemicals by measuring exposure markers, chemicals or their metabolites, in human urine, blood, serum, and other body fluids. However, the metabolism of chemicals within an organism is extremely complex. Therefore, the identification of metabolites is often difficult and laborious. Several untargeted metabolomics methods have been developed to perform objective searching/filtering of accurate-mass-based LC-MS data to facilitate metabolite identification. In this study, three metabolomics data processing approaches were used for chemical exposure marker discovery in urine with an LTQ-Orbitrap high-resolution mass spectrometry (HRMS) dataset; di-isononyl phthalate (DINP) was used as an example. The data processing techniques included the SMAIT, mass defect filtering (MDF), and XCMS Online. Sixteen, 83, and 139 probable DINP metabolite signals were obtained using the SMAIT, MDF, and XCMS procedures, respectively. Fourteen probable metabolite signals mined simultaneously by the three metabolomics approaches were confirmed as DINP metabolites by structural information provided by LC-MS/MS. Among them, 13 probable metabolite signals were validated as exposure-related markers in a rat model. Six (m/z 319.155, 361.127, 373.126, 389.157, 437.112 and 443.130) of the 13 exposure-related DINP metabolite signals have not previously been reported in the literature. Our data indicate that SMAIT provided an efficient method to discover effectively and systematically urinary exposure markers of toxicant. The DINP metabolism information can provide valuable information for further investigations of DINP toxicity, toxicokinetics, exposure assessment, and human health effects.     

催化裂化催化剂上污染重金属含量测定的XRF光谱分析方法的研究

介绍了用 X射线荧光光谱测定催化裂化平衡催化剂上污染重金属 Fe、Ni、V、Cu、Sb和 Ca含量的分析方法。考查了影响 Fe、Ni等元素测定的各种因素 ,提出以新鲜催化剂为配制标样的载体 ,较好地克服了元素间互相干扰的影响 ,减少基体效应 ,取得了 Fe、Ni等元素含量的准确结果。实验结果表明 ,XRF光谱法测定催化剂上污染重金属元素的含量是一种快速、准确、简便的分析方法