Adsorption enthalpy and desorption enthalpy during displacement of adsorbate to solvent in a liquid-solid system

The adsorption heat of the stoichiometric displacement process for the adsorption of a solute in a liquid-solid system was investigated. On the basis of the SDM-A and the rule of the additivity of energy, an expression which describes the dependence of the adsorption enthalpy on the nature and concentration of the solute, and on the solvent and adsorbent, was derived. The adsorption heat determined for the solute with the traditional method can be divided into two independent fractions, relating to the adsorption of the solute and to the desorption of the solvent. Experimental data on both isotherms from the literatures and precise calorimetry were used to test the adsorption heat and its fractions computed quantitatively via the equations presented in this study, and a satisfactory degree of conformity between them was obtained. Supported by the Natural Science Foundation of Shaanxi Province in China.     

斜圈弹簧力学性能的有限元分析

斜圈弹簧在医疗器械、高压开关、汽车工业等领域应用广泛. 但其结构特殊, 受力复杂, 目前尚无有效的理论计算方法得出其载荷位移曲线, 只能通过数值仿真的方法研究其力学性能. 利用有限元软件ANSYS参数化建立环形斜圈弹簧有限元模型, 通过对模型的分析求解, 得出了其主要参数线径、节距、倾斜角与斜圈弹簧力学性能之间的关系. 研究了斜圈弹簧工作状态下的受力变形情况, 计算分析结果为斜圈弹簧的优化设计和合理应用提供了理论依据.     

Multi-Step Continuous-Flow Organic Synthesis: Opportunities and Challenges

Continuous-flow multi-step synthesis takes the advantages of microchannel flow chemistry and may transform the conventional multi-step organic synthesis by using integrated synthetic systems. To realize the goal, however, innovative chemical methods and techniques are urgently required to meet the significant remaining challenges. In the past few years, by using green reactions, telescoped chemical design, and/or novel in-line separation techniques, major and rapid advancement has been made in this direction. This minireview summarizes the most recent reports (2017–2020) on continuous-flow synthesis of functional molecules. Notably, several complex active pharmaceutical ingredients (APIs) have been prepared by the continuous-flow approach. Key technologies to the successes and remaining challenges are discussed. These results exemplified the feasibility of using modern continuous-flow chemistry for complex synthetic targets, and bode well for the future development of integrated, automated artificial synthetic systems.     

用红外激光脉冲触发半绝缘GaAs光电导开关的实验研究

报道了用光子能量低于GaAs禁带宽度的红外激光脉冲,触发电极间隙为3mm和8mm的半绝缘GaAs光电导开关的实验结果。使用单脉冲能量为1.9mJ的1 064nm Nd:YAG激光触发开关, 在偏置电压分别为3kV和5kV条件下,光电导开关分别工作于线性和非线性模式。用900nm半导体激光器和1 530nm掺铒光纤激光器分别进行触发实验,得到了重复频率分别为5kHz和20MHz的电脉冲波形。结果表明,半绝缘GaAs光电导开关可以吸收大于本征吸收限波长红外激光脉冲。     

金刚石衬底上GaN HEMT沟道温度建模:各向异性且非均匀热导率的影响

为了改善GaN HEMT的自热效应,集成高热导率的金刚石衬底有助于增强器件有源区的热量耗散。然而,化学气相淀积(CVD)生长的多晶金刚石(PCD)具有柱状晶粒结构,导致了各向异性的材料热导率,且其热导率值与生长厚度有关。为此,通过建模金刚石生长过程中晶粒尺寸的演变过程,计算了金刚石沿面内和截面方向的热导率。基于该PCD热导率模型,利用计入材料非线性热导率的GaN器件热阻解析模型,计算得到了GaN HEMT沟道温度的波动范围,并分析了其与器件结构(栅长、栅宽、栅间距、衬底厚度)和功耗的依赖关系。最后,通过与有限元(FEM)仿真结果对比,分区域提取了GaN HEMT器件中PCD衬底的有效热导率,分别为260~310 W/(m·K)和1 250~1 450 W/(m·K)。本文的计算为预测金刚石衬底上GaN HEMT器件的沟道温度提供了快速、有效的方法。     

基于数值模拟的CZSi单晶收尾控制参数研究

采用理论分析和有限元数值模拟相结合的方法研究了晶体收尾过程中的温度分布与热量传递.解释了"倒草帽"形收尾(收尾前段晶体直径猛然收缩)的成因,指出了改进收尾形状的方法,研究结果对于合理设定直拉硅单晶收尾工艺参数具有一定的参考意义.通过对比试验,仿真计算结果与单晶炉实验测试结果相吻合.     

Monte Carlo方法模拟非直视紫外光散射覆盖范围

针对大气中紫外光散射通信的特点, 用Monte Carlo方法对紫外光非直视(NLOS) 通信三种工作方式的覆盖范围进行分析, 建立了基于Monte Carlo方法的NLOS紫外光传输模型.利用Monte Carlo模拟方法对三种NLOS散射方式的单次和多次散射路径损耗及覆盖范围进行模拟研究, 结果表明, 多次散射和单次散射的路径损耗基本一致, NLOS(a) 类全向发送全向接收通信方式覆盖范围最小但全方位性好, NLOS(b) 类定向发送全向接收通信方式的覆盖范围较大但有一定方向性, NLOS(c) 类定向发送定向接收通信方式的覆盖范围最大但有很强的方向性.     

MOVPE生长的InGaN/GaN单量子阱的光致发光和光吸收特性

研究了用金属有机物气相外延(MOVPE)法在蓝宝石衬底上生长的In组分浓度保持不变的InGaN/GaN单量子阱结构在室温下的发光特性和光吸收特性.实验结果表明,在InGaN厚度<3nm时,随着样品InGaN势阱层宽度的增加(1nm),光致发光(PL)谱的发光峰值波长出现明显的红移33nm现象,而且发光强度下降8%,谱线半峰全宽(FWHM)展宽,通过对样品的透射、反射光谱研究发现,量子阱层窄(1.5nm)的样品在波长接近红外区时出现无吸收的现象,即R+T达到了100%,而在阱层较宽的样品中没有发现这一现象,对引起这些现象的原因进行了讨论.这些结果有助于开发和优化三族氮化物半导体光电器件的进一步研究工作.     

新型毛细管内固相萃取-气相色谱法检测纺织品中烷基酚类物质

建立了毛细管内固相萃取(SPE)-气相色谱(GC)检测纺织品中壬基酚和辛基酚含量的分析方法。通过比较4种性质不同固相萃取剂的萃取效果,筛选出对烷基酚(APs)类物质萃取效果最佳的固相萃取剂,将其作为填充物质制作毛细管内固相萃取柱,将毛细管内固相萃取法与气相色谱联用进行分析检测。最佳固相萃取剂为Abselut NEXUS,毛细管内固相萃取最佳条件为:1.2 μL甲醇和1.2 μL超纯水活化,1.2 μL甲醇洗脱,上样速率是0.4 μL/min。该法在较低浓度范围内呈现良好的线性相关性,对烷基酚的富集倍数约为100倍,对辛基酚和壬基酚的检出限分别为3.7 μg/L和4.5 μg/L,加标回收率分别为85.6%~98.2%和83.8%~95.7%,结果表明,此法能够简捷、迅速、有效地检测出纺织品中残留的烷基酚类物质。     

N503为载体的支撑液膜体系中汞(Ⅱ)的迁移研究

研究了以多孔聚偏氟乙烯为支撑体,N503为膜载体,煤油为膜溶剂的支撑液膜体系中Hg(Ⅱ)的迁移行为,测定了Hg(Ⅱ)与N503在煤油溶剂中的萃合物组成和条件萃取常数,考察了料液相pH值、载体浓度、料液相及反萃相中Cl-浓度等因素对Hg(Ⅱ)迁移的影响,获得Hg(Ⅱ)迁移的最佳条件:料液相pH=2.5～3.0,Cl-浓度为0.1 mol/L,载体浓度为0.706 mol/L,反萃相中Cl-浓度为0.8 mol/L.在最佳实验条件下,当Hg(Ⅱ)起始浓度为5.0×10-5 mol/L时,迁移120 min,Hg(Ⅱ)的迁移率可达99.6%.Hg(Ⅱ)在N503-煤油支撑液膜体系中的扩散层厚度δa为1.57×10-5 m,膜内扩散系数d0为7.26×10-13 m2/s,确立了Hg(Ⅱ) 的渗透系数P方程.