HL-2A托卡马克上的边缘局域模特性初步研究

高约束模式(H模)下自发产生的边缘局域模(ELM),虽然利于控制等离子体密度和排出杂质粒子从而实现H模放电的稳态运行,但是ELM爆发携带的大量粒子和能量会对装置的第一壁材料造成很大的损坏,所以在下一代聚变装置上使用之前很多装置已经开始了对ELM的研究.在HL-2A装置上观察到了不同的ELM,扰动幅度小的ELM引起的等离子体储能损失小于3%,ELM之间的时间间隔约为3 ms,表现出Ⅲ型ELM的特征;扰动幅度较大的ELM的爆发对等离子体电流、等离子体密度及储能都有很明显的扰动,对等离子体储能的扰动大于10%,ELM爆发的频率随通过等离子体磁分界面的净加热功率的增加而增加,表现出明显的Ⅰ型ELM的特征.ELM先兆有不对称性,在弱场侧磁探针信号能观测到,但强场侧却观测不到;ELM先兆的频率约为45 kHz,观测到的最长的先兆先于ELM前约10ms出现.     

Highly Active La(III)-Based Metal-Organic Framework as a Heterogeneous Lewis Acid Catalyst for Friedel-Crafts Alkylation

In this study, a novel La(III)-based two-dimensional (2D) metal-organic framework, [La_2/3(qptca)_1/2] (referred to as SLX-2), from LaCl₃ and 1,1′ : 4′,1′′ : 4′′,1′′′ : 4′′′,1′′′′-quinquephenyl]-2,2′′,2′′′′,5′′-tetracarboxylic acid (H₄qptca) was synthesized by conventional solvothermal method and thoroughly characterized by using X-ray single-crystal diffraction, powder X-ray diffraction, and thermogravimetric analyses. The 2D SLX-2 features a unique lanthanum center exposed to the skeleton and was used as an efficient Lewis acid catalyst for the Friedel-Crafts alkylation of indole and pyrrole with β-nitrostyrene along with a wide substrate scope, giving the desired products in good-to-high yields under the optimal reaction conditions. Furthermore, the catalyst was used for twenty cycles, with nearly no effect on its activity, and the reaction was heterogeneous in nature. Moreover, compared to the previous hydrogen-bond-donating MOF catalysts for such alkylation reactions, SLX-2 showed an excellent stability toward harsh acidic and basic environment, and gave comparable catalytic activities.     

SiO2阶层多孔结构搭建及块体材料制备机理

借助溶胶-凝胶结合相分离和模板法进行了阶层多孔结构的搭建及二氧化硅多孔块体材料的制备,表征了阶层多孔块体的显微结构及孔结构特性,分析了阶层多孔结构的搭建机理。研究结果表明,三嵌段共聚物聚环氧乙烷-聚环氧丙烷-聚环氧乙烷（P123）的加入不仅诱导共混体系发生相分离,调控大孔结构的形成,同时形成球形胶束并作为模板剂进入骨架,而1,3,5-三甲基苯（TMB）的加入使P123形成的胶束膨胀且更加稳定,在骨架上成功引入了球形介孔,骨架中凝胶粒子相互聚集形成微孔,从而搭建贯通大孔-球形介孔-微孔同时分布的阶层多孔结构,并获得相应的多孔块体材料;当正硅酸甲酯（TMOS）：P123：TMB摩尔比为1：0.015：0.353时,多孔块体材料的阶层多孔结构最优,大孔孔径为0.5-1.5 μm,介孔孔径为3-4 nm,显气孔率66.1%,比表面积为616 m²·g^-1。     

2H-吡咯的简易合成方法:金催化与路易斯酸催化的组合应用

报道了利用金催化与铜催化相结合合成5-氨基-2H-吡咯的方法. 首先通过均相金催化异恶唑与炔酰胺反应生成α-亚胺金卡宾中间体, 再经[3+2]环加成反应合成并分离出5-氨基-3H-吡咯, 然后通过铜催化的去酰基化和基团迁移反应来实现3H-吡咯向2H-吡咯的转化. 该方法不但操作简单、反应条件温和、官能团兼容性良好, 而且还能进行克量级放大. 这项研究为合成具有重要生物活性的5-氨基-2H-吡咯化合物提供了广谱实用的合成方法.     

RP-3替代燃料自点火燃烧机理构建及动力学模拟

通过对RP-3 航空煤油成分的分析, 以及对8 组替代模型的对比实验, 选取了73.0%(质量分数)正十二烷, 14.7% 1,3,5-三甲基环己烷, 12.3%正丙基苯作为RP-3 航空煤油的替代模型. 使用本课题组自主研发的机理自动生成程序ReaxGen, 构建了RP-3 替代燃料的高温燃烧详细机理, 用该机理模拟了激波管点火延时, 并与实验数据进行比较. 用物质产率分析和近似轨迹优化算法(ATOA)简化方法简化了详细机理. 最后对燃烧机理在不同化学计量比及压力条件下的点火延时做了敏感度分析, 考察了燃烧机理在不同化学计量比下关键反应的异同. 结果表明, 该替代模型的燃烧机理能很好地描述RP-3煤油的高温点火特性.     

Optoelectronic characterisation of an individual ZnO nanowire in contact with a micro-grid template

Optoelectronic characterisation of an individual ZnO nanowire in contact with a micro-grid template has been studied.The low-cost micro-grid template made by photolithography is used to fabricate the ohmic contact metal electrodes.The current increases linearly with the bias,indicating good ohmic contacts between the nanowire and the electrodes.The resistivity of the ZnO nanowire is calculated to be 3.8 ·cm.We investigate the photoresponses of an individual ZnO nanowire under different light illumination using light emitting diodes(λ = 505 nm,460 nm,375 nm) as excitation sources in atmosphere.When individual ZnO nanowire is exposured to different light irradiation,we find that it is extremely sensitive to UV illumination;the conductance is much larger upon UV illumination than that in the dark at room temperature.This phenomenon may be related to the surface oxygen molecule adsorbtion,which indicates their potential application to the optoelectronic switching device.     

Homotopic mapping method of solitary wave solutions for generalized complex Burgers equation

A class of generalized complex Burgers equation is considered. First, a set of equations of the complex value functions are solved by using the homotopic mapping method. The approximate solution for the original generalized complex Burgers equation is obtained. This method can find the approximation of arbitrary order of precision simply and reliably.     

基于色散效应的光纤光栅高速高精度解调方法研究

利用普通单模光纤(SMF)与色散补偿光纤(DCF)分别具有正色散和负色散系数特性,实现光纤光栅阵列的高速高精度解调.系统采用全光纤结构,仅需发出单一高速光脉冲,即可根据反射光脉冲时延差同时获取各个光栅的波长与位置信息,大幅提高了光纤光栅解调速度;通过建立DCF-SMF双通道和色散差矫正模型,削弱了温度变化及色散值误差对系统解调精度的影响.实验表明,本方法解调速率可达1 MHz,解调过程受传感网络光纤及双通道温变影响较小,具有良好稳定性及高精度;5—75?C温度扰动实验中,传感网络传输光纤温变时系统解调均方差16.8 pm,DCF-SMF双通道受温度扰动时系统解调均方差为11.9 pm,恒温下系统长时间解调时均方差为6.4 pm;应力实验中,解调线性度可达0.9998,解调精度约为8.5 pm.     

AOT/Triton X-100混合反胶束体系的导电性能

采用聚乙二醇辛基苯基醚(TritonX-100)和二(2-乙基己基)琥珀酸磺酸钠(AOT)双表面活性剂,与正己烷、正己醇和水构成混合反胶束体系;研究了表面活性剂质量比、助表面活性剂含量、水油体积比和温度等因素对反胶束体系导电性能的影响,同时采用循环伏安法研究了K3Fe(CN)6/K4Fe(CN)6在该体系中的电化学行为.结果表明:由两种表面活性剂构成的反胶束体系电导率σ明显大于单一表面活性剂反胶束体系电导率;体系电导率随AOT与TritonX-100的质量比w(w=mAOT∶mTritonX-100)的变化而变化,w为0-0.4时,电导率随w增大而线性增大,之后增加趋势变缓;w=0.96时,σ达到稳定值576μS·cm-1.混合体系电导率随溶水量的增大及温度的上升而提高;而增加助表面活性剂可显著降低体系的电导率.在所研究体系中,Fe(CN)36-/Fe(CN)46-电化学反应对的氧化还原峰电位几乎不随扫描速率变化,峰电位差约为75mV,峰电流的比值约为1,氧化峰电流与扫描速率的平方根成正比,说明K3Fe(CN)6/K4Fe(CN)6在混合反胶束体系中显示出良好的氧化还原可逆性,反应由扩散步骤控制.