1-(4-氯苯基)-2-环丙基酮肟醚的设计、合成及杀虫活性

采用中间体衍生化方法,以环唑醇中间体1-(4-氯苯基)-2-环丙基丙酮作为基本骨架,引入肟醚活性片段,合成了32个新的1-(4-氯苯基)-2-环丙基酮肟醚类化合物,其化学结构经核磁共振波谱和质谱等确认.单晶X衍射分析表明,化合物2n属于单斜晶系,空间群为P21/c.生物活性筛选结果表明,化合物1i在200mg/L浓度下对蚜虫的致死率为78. 57%;化合物1g在200 mg/L浓度下对红蜘蛛的致死率为69. 95%;化合物1i在200和12. 5 mg/L浓度下对黏虫的致死率分别为100%和85%.     

岩石、混凝土类材料断裂破坏有限元数值模拟中的有效方法

岩石、混凝土类材料断裂破坏有限元数值模拟中的网格重划,依据单元畸变和裂缝介质间的单元干涉作为网格重划判据,采用几何体重构技术把几何实体分解成能在ANSYS上实现六面体网格划分的几个部分,利用体积判断法确定新结点在旧单元的单元编号,在场量传递上采用基于解析性质的等参有限元逆变换,把旧网格场量信息传递到新网格中。本文对ANSYS进行二次开发,实现了三维网格重划,网格重划采用单元畸变和界面干涉两个判据,在网格再划分前进行几何体重构,提取变形后的点线面信息重新生成实体,充分利用AN-SYS的函数和体积判断法找到新结点在旧网格中的位置,在新旧网格间的场量传递中采用基于解析逆等参单元法。在平台上实现了三维有限元网格重划技术,最后利用方料的单轴压缩断裂模拟计算检验了传递前后等效塑性应变分布用载荷信息的变化,证明了所开发系统的正确性。     

R134a在板式换热器中的凝结换热实验研究

本文对R134a在板式换热器内的凝结换热特性进行了实验研究,通过测量换热器中冷却水及板壁温度获得了局部凝结换热系数随蒸气干度、质量流量及热流密度的变化关系.实验结果表明,凝结换热系数随着蒸气干度增加而增加.文章还将实验结果与部分文献数据进行了比较与分析.本文的研究为换热准则关系式的发展提供了实验数据.     

铀床氚残留量的测量

分别采用直接测量法、同位素交换法和溶解法测量铀床中的氚残留量, 并分析了这三种测量方法在本实验条件下的误差. 直接测量法测量铀床的氚残留量的结果如下: 铀床的氚残留量为2.68%, 即每克铀含(0.0308±0.0003) mmol 氚气; 当压力读数在1500～133332 Pa之间时, 基于理想气体状态方程的测量方法(简称PVT法)的标准差小于0.95%. 同位素交换法测量铀床氚的结果如下: 加热充分解吸过的铀床经多次同位素交换后, 其交换效率仅为2.84%, 即不到3%(摩尔分数)的氚被氘气载带出来, 其同位素交换法测量的标准差为7.35%. 溶解法能够彻底地测量铀床中残留的氚, 其溶解法测量的标准差为6.49%.     

基于改进的空域相关的多聚焦图像融合

提出了一种简单有效的像素级多聚焦图像融合方法。针对正交小波变换缺乏平移不变性而产生视觉失真的缺陷,采用Atrous算法将原图像分解在不同频率域上。Atrous算法先将滤波器h0(n),h1(n)各点间插入适当的零值后再与低频信号做卷积,故又称为"多孔算法"。将具有抑制噪声性能的空阈相关法作为高频子图像的融合规则,选取相关性强边缘特征显著的点作为最终融合子图像的像素点。实验表明,由此融合的图像能完好的保留边缘纹理信息。融合后的图像在客观评价和主管视觉效果上均有提高。     

3D Uranyl Organic Frameworks Supported by Rigid Octadentate Carboxylate Ligand: Synthesis,Structure Diversity,and Luminescence Properties

Seven three dimensional (3D) uranyl organic frameworks (UOFs), formulated as [NH₄][(UO₂)₃(HTTDS)(H₂O)] ( 1 ), [(UO₂)₄(HTTDS)₂](HIM)₆ ( 2 , IM=imidazole), [(UO₂)₄(TTDS)(H₂O)₂(Phen)₂] ( 3 , Phen=1,10-phenanthroline), [Zn(H₂O)₄]_0.5[(UO₂)₃(HTTDS)(H₂O)₄] ( 4 ), and {(UO₂)₂[Zn(H₂O)₃]₂(TTDS)} ( 5 ), {Zn(UO₂)₂(H₂O)(Dib)_0.5(HDib)(HTTDS)} ( 6 , Dib=1,4-di(1H-imidazol-1-yl)benzene) and [Na]{(UO₂)₄[Cu₃(u₃-OH)(H₂O)₇](TTDS)₂} ( 7 ) have been hydrothermally prepared using a rigid octadentate carboxylate ligand, tetrakis(3,5-dicarboxyphenyl)silicon(H₈TTDS). These UOFs have different 3D self-assembled structures as a function of co-ligands, structure-directing agents and transition metals. The structure of 1 has an infinite ribbon formed by the UO₇ pentagonal bipyramid bridged by carboxylate groups. With further introduction of auxiliary N-donor ligands, different structure of 2 and 3 are formed, in 2 the imidazole serves as space filler, while in 3 the Phen are bound to [UO₂]²⁺ units as co-ligands. The second metal centers were introduced in the syntheses of 4–7 , and in all cases, they are part of the final structures, either as a counterion ( 4 ) or as a component of framework ( 5 − 7 ). Interesting, in 7 , a rare polyoxometalate [Cu₃(μ₃-OH)O₇(O₂CR)₄] cluster was found in the structure. It acts as an inorganic building unit together with the dimer [(UO₂)₂(O₂CR)₄] unit. Those uranyl carboxylates were sufficiently determined by single crystal X-ray diffraction, and their topological structures and luminescence properties were analyzed in detail.     

Research on Lateral Vibration Coupling Mechanism of a High-Speed Train Based on Singular Coefficients

Russian Physics Journal - The lateral vibration coupling mechanism is the basic law describing the current vibration behavior of a high-speed train. The main reason is that there are design defects...     

Metal-Organic Frameworks with Novel Catenane-like Interlocking: Metal-Determined Photoresponse and Uranyl Sensing

The assembly of two tripyridinium-tricarboxylate ligands and different metal ions leads to seven isostructural MOFs, which show novel 2D→2D supramolecular entanglement featuring catenane-like interlocking of tricyclic cages. The MOFs show tripyridinium-afforded and metal-modulated photoresponsive properties. The MOFs with d¹⁰ metal centers ( 1-Cd , 1-Zn , 2-Cd , 2-Zn ) show fast and reversible photochromism and concomitant fluorescence quenching, 1-Ni displays slower photochromism but does not fluoresce, and 1-Co and 2-Co are neither photochromic nor fluorescent. It is shown here that the network entanglement dictates donor-acceptor close contacts, which enable fluorescence originated from interligand charge transfer. The contacts also allow photoinduced electron transfer, which underlies photochromism and concomitant fluorescence response. The metal dependence in fluorescence and photochromism can be related to energy transfer through metal-centered d-d transitions. In addition, 1-Cd is demonstrated to be a potential fluorescence sensor for sensitive and selective detection of UO₂²⁺ in water.     

温度对NH3气体紫外吸收截面影响研究

为了研究NH3气体在紫外203～220 nm内吸收截面随温度的变化规律,采用高分辨率光栅单色仪、氘灯光源、闭式气样室和配气装置,测量NH3气体温度由308 K升高至397 K的吸收截面.NH3气体吸收截面由离散吸收和连续吸收两部分组成.结果表明,随着温度的升高,基态剩余量子旋转、振动迁移到激发态的概率减少,最终导致离散吸收截面峰值的降低.随着温度由308 K升高至397 K,在特征波长212.5 nm处,离散吸收截面峰值的最大相对减幅为46%.NH3气体在这个波段的吸收截面存在明显的等波长间隔分布特征,约为4 nm.随着温度升高,峰值位置未见变化.连续吸收截面整体上随温度升高而减小,且这种减小趋势随波长红移逐渐减弱.由于NH3气体吸收截面随温度的变化呈现较大的变化,实测时应对气体浓度在线测量结果进行温度补偿计算.     

反映时序特征的听神经自发发放模型

听神经发放时序在听信息编码中起重要作用,要认识和运用听觉系统对听神经发放时序特征的利用机制必须对听神经发放时序特征有认识,但是已有的随机过程数学模型均不能很好地反映听神经发放时序特征。而关于发放的生理模型,如Hodgkin-Huxley方程、Meddis模型对发放过程的描述均是决定性的、连续性的,不能反映生理过程的离散性和发放过程的随机性。本文基于神经发放生理过程,通过对神经发放条件以及自发发放时神经递质释放时序的描述,建立了一个简单自发发放模型。模型在很好地反映听神经自发发放时序外部统计特征的同时,所得到的神经递质的释放速率在生理上也是合理的。模型还能对纯音激励时听神经的锁相发放做出定性解释,可作为进一步研究反映时序特征的有激励发放模型的基础。