有限元网格自动生成及自动调整技术

本文给出了一种任意平面域内三角形网格自动生成及自动调整算法，并编制了相应的程序。通过对带Ｕ形槽的三点变曲试件的分析，证明本文算法是可行的，并且具有稳定性能好、收敛速度快的优点。     

溴酚蓝和亚甲蓝双显色体系萃取光度法测定铜

向三元络合物[Cu(phen)_3)BPB的二氯乙烷萃取液中,加入KCN水溶液,形成的[Cu(CN)_2)~-和溴酚蓝离子(BPB)进入水相,向其中加入与BPB颜色相近的亚甲蓝(MB)再进行萃取光度测定。因萃取液中[MB_2BPB)和[Cu(CN)_2)MB两者的吸光作用,使本方法具有很高的灵敏度,ε=1.77×10~5L·mol~(-1)·cm~(-1)。铜含量在0～5μg/25ml遵从比耳定律,对含铜量为10~(-8)g/ml的水样测定5次,相对标准偏差为2％。     

Syntheses,crystal structures and magnetic properties of two new cyano-bridged bimetallic complexes

Transition Metal Chemistry - Two complexes [Fe(1,10-phen)2Ni(CN)4]n (1), {[Fe2(1,10-phen)4(CN)4Co2(1,10-phen)2Fe(CN)6]·2H2O}n (2) were prepared in the reaction of K3[Fe(CN)6] as cyanometalate...     

Valency‐Controlled Framework Nucleic Acid Signal Amplifiers

Weak ligand–receptor recognition events are often amplified by recruiting multiple regulatory biomolecules to the action site in biological systems. However, signal amplification in in vitro biomimetic systems generally lack the spatiotemporal regulation in vivo. Herein we report a framework nucleic acid (FNA)‐programmed strategy to develop valence‐controlled signal amplifiers with high modularity for ultrasensitive biosensing. We demonstrated that the FNA‐programmed signal amplifiers could recruit nucleic acids, proteins, and inorganic nanoparticles in a stoichiometric manner. The valence‐controlled signal amplifier enhanced the quantification ability of electrochemical biosensors, and enabled ultrasensitive detection of tumor‐relevant circulating free DNA (cfDNA) with sensitivity enhancement of 3–5 orders of magnitude and improved dynamic range.     

氢化物-非色散原子荧光法测定饲料矿物添加剂中的砷

本文采用氢化物－非色散原子荧光光谱法研究了十几种饲料矿物添加剂中金属离子对砷测定的干扰，采用加入硫脲－抗坏血酸混合溶液、碘化钾分离、加热蒸干等方法消除干扰。同时本文还对测定砷的酸度、硼氢化钾浓度和仪器工作参数进行了研究和优化。方法相对标准偏差（RSD）为0．54％，检出限（D．L）为54．5ng/L，样品国．加标回收率为102．9％。实际样品测定结果与胂斑法相比具有很好的一致性。     

太赫兹互补金属氧化物半导体场效应管探测器理论模型中扩散效应研究

针对基于经典动力学理论传统模型中忽略扩散效应的问题,通过对基于玻尔兹曼理论的场效应管传输线模型的理论分析,建立了包含扩散效应的太赫兹互补金属氧化物半导体(CMOS)场效应管探测器理论模型,研究扩散效应对场效应管电导及响应度的影响.同时,将此模型与忽略了扩散效应的传统模型进行了对比仿真模拟,给出了两种模型下的电流响应度随温度及频率变化的差别.依据仿真结果,并结合3σ原则明确了场效应管传输线模型中扩散部分省略的依据和条件.研究结果表明:扩散部分引起的响应度差异大小主要由场效应管的工作温度及工作频率决定.其中工作频率起主要作用,温度变化对差异大小影响较为微弱;而对于工作频率而言,当场效应管工作频率小于1 THz时,模型中的扩散部分可以忽略不计;而当工作频率大于1 THz时,扩散部分不可省略,此时场效应管模型需同时包含漂移、散射及扩散三个物理过程.本文的研究结果为太赫兹CMOS场效应管理论模型的精确建立及模拟提供了理论支持.     

磁粉法检测表面裂纹概率曲线的测定

本文介绍了利用实物零件测定裂纹检出概率的方法，并作出了用磁粉法检测表面裂纹的检测概率曲线，为大型构件检测周期的确定提供了可靠数据，为结构损伤容限设计，可靠性设计提供了重要的依据。     

浸没沉淀相转化法制备结晶性聚合物微孔膜的研究进展

综述了近期关于结晶性聚合物浸没沉淀相转化法制备微孔膜的成膜机理和实验研究工作.对制膜体系的热力学、相分离、成膜机理进行了分析和总结,并依此解析了结晶性聚合物膜中常见的结构形态,最后从热力学和动力学两个方面对影响膜结构形态的因素如聚合物的浓度、铸膜液的组成、凝固浴的组成等进行了详细的讨论.     

Ultrafast time-resolved study of photophysical processes involved in the photodeprotection of p-hydroxyphenacyl caged phototrigger compounds

A combined femtosecond Kerr gated time-resolved fluorescence (fs-KTRF) and picosecond Kerr gated time-resolved resonance Raman (ps-KTR(3)) study is reported for two p-hydroxyphenacyl (pHP) caged phototriggers, HPDP and HPA, in neat acetonitrile and water/acetonitrile (1:1 by volume) solvents. Fs-KTRF spectroscopy was employed to characterize the spectral properties and dynamics of the singlet excited states, and the ps-KTR(3) was used to monitor the formation and subsequent reaction of triplet state. These results provide important evidence for elucidation of the initial steps for the pHP deprotection mechanism. An improved fs-KTRF setup was developed to extend its detectable spectral range down to the 270 nm UV region while still covering the visible region up to 600 nm. This combined with the advantage of KTRF in directly monitoring the temporal evolution of the overall fluorescence profile enables the first time-resolved observation of dual fluorescence for pHP phototriggers upon 267 nm excitation. The two emitting components were assigned to originate from the (1)pipi (S(3)) and (1)npi (S(1)) states, respectively. This was based on the lifetime, the spectral location, and how these varied with the type of solvent. By correlating the dynamics of the singlet decay with the triplet formation, a direct (1)npi --> (3)pipi ISC mechanism was found for these compounds with the ISC rate estimated to be approximately 5 x 10(11) s(-)(1) in both solvent systems. These photophysical processes were found to be little affected by the kind of leaving group indicating the common local pHP chromophore is largely responsible for the fluorescence and relevant deactivation processes. The triplet lifetime was found to be approximately 420 and 2130 ps for HPDP and HPA, respectively, in the mixed solvent compared to 150 and 137 ns, respectively, in neat MeCN. The solvent and leaving group dependent quenching of the triplet is believed to be associated with the pHP deprotection photochemistry and indicates that the triplet is the reactive precursor for pHP photorelease reactions for the compounds examined in this study.     

Two 2D uranyl coordination complexes showing effective photocatalytic degradation of Rhodamine B and mechanism study

Two new hydrostable two-dimensional(2 D) uranyl coordination complexes [(UO_2)_5(μ_3-O)_2(nbca)_2].7 H_2O(1) and [(UO_2)_3(nbca)_2(H_2O)_3]·2 H_2O(2)(H_3 nbca=5-nitro-1,2,3-benzenetricarboxylic acid) were hydrothermal synthesized.Single-crystal structural refinements reveal that both of the two complexes were formed by the packing of 2D uranyl coordination sheets via the hydrogen bonds.The nbca ligand coordinating to the uranyl polyhedron centers constructed the 2D sheets.There are UO_8 hexagonal bipyramids and UO_7 pentagonal bipyramids in 1 while only U07 pentagonal bipyramids in 2.Photocatalytic degradation of rhodamine B(RhB) in aqueous solution was studied.Complex 2 possesses better performance than 1 with 96.2 % of the RhB was degraded in only 60 min.Mechanism studies reveal that the dissolved oxygens are essential to the RhB degradation.The photocurrent density of 2 is more stable than that of 1,which indicating the stronger ability to separate photoexcited electrons and hole pairs of 2.