基于FAIMS谱图峰位置的离子迁移率非线性函数解析

离子迁移率的非线性函数反映了物质本身的微观碰撞特性,是FAIMS技术实现离子分离检测的基础。现有的离子迁移率非线性函数求解方法多是近似求解,存在较大误差。该工作提出了一种基于半正弦分离电压和FAIMS谱图峰位置下的严格求解方法,推导出严格的二阶、四阶系数求解方程。利用自制的高场不对称波形离子迁移谱仪分别对乙醇、间二甲苯和正丁醇三种典型的醇和苯类物质进行检测,获取了三种物质的FAIMS谱图,通过谱图峰位置获得了不同分离电压值下的补偿电压,利用最小二乘法求出三种离子非线性函数二阶、四阶系数。拟合后的均方误差表明FAIMS非线性函数严格求解的方法,明显优于现有的求解方法。有助于提高FAIMS检测分辨率,进而有助于建立更加准确的FAIMS图谱,实现FAIMS对检测物质的精准识别。     

Interference of dissociating wave packets in the I2 molecule driven by femtosecond laser pulses

The interference between two dissociating wave packets of the I2 molecule driven by femtosecond laser pulses is theoretically studied by using the time-dependent quantum wave packet method.Both the internuclear distanceand velocity-dependent density functions are calculated and discussed.It is demonstrated that the interference pattern is determined by the phase difference and the delay time between two pump pulses.With two identical pulses with a delay time of 305 fs and a FWHM of 20 fs,more interference fringes can be observed,while with two pump pulses with a delay time of 80 fs and a FWHM of 20 fs,only a few interference fringes can be observed.     

Ni/Ni3Al interface: A density functional theory study

The optimal geometries, mechanical and thermal properties, and electronic structures of the three low index (0 0 1), (1 1 0), (1 1 1) Ni/Ni₃Al thin film were studied using first principle calculations. Simulated results indicated that Ni and Al atoms in γ^′ phase preferred to place in the hollow site of Ni atoms in γ phase. In hollow site models, electronic states affected by interface localize within 2 atomic layers. While the top site model, electronic states localize within 3 atomic layers. It is also found that hollow site (1 1 0) interface has the best mechanical properties. Hollow site (0 0 1) interface is the most easily formed interface, which has the best thermodynamic properties.     

“强光一号”Al丝阵Z箍缩产生K层辐射实验研究

在“强光一号”加速器开展了Al丝阵Z箍缩产生K层辐射的实验研究,固定Al丝线径20 μm、丝阵直径12 mm,丝根数为8和12的负载获得K层产额分别为0.9 kJ/cm和1.1 kJ/cm,明显高于16和24根丝负载.辐射功率波形和时间分辨的X射线图像显示,低丝数负载存在拖尾质量引起的多次内爆现象.在60%—80%的内爆时间内,丝阵几乎停留在初始位置;主体内爆在随后的25—30 ns内完成,将部分等离子体留在初始位置,形成质量的拖尾分布;内爆后期驱动电流向外围的拖尾质量迁移,引 关键词： Al丝阵 Z箍缩 K层辐射')" href="#">K层辐射 拖尾质量     

基于三维有限元法模拟分析六面顶顶锤的热应力

以有限元法为理论分析手段模拟分析了国产六面顶压机配套顶锤内部的温度场和热应力分布.探寻出了XKY-6×2000 MN型六面顶压机顶锤内部的温度场分布以及热应力取值.模拟结果表明加热顶锤内部温度分布不均匀,不均匀的温度分布产生了热剪切应力,热剪切应力峰值达到0.62 GPa,分布在41.5°小斜面上.加热顶锤内部的剪切应力值较非加热锤内部的剪切应力值高出18.0％.模拟分析结果与金刚石的高压合成实验事实相符,在理论上解释了加热顶锤使用寿命较非加热顶锤使用寿命短的原因,此项工作对于提高大顶锤使用寿命,降低生产 关键词： 热应力 顶锤 有限元法 工业金刚石     

高压作用下相分离液体玻璃转变的分子动力学研究

采用分子动力学模拟方法,研究了二元混合液体在不同外压作用下的相分离与玻璃转变过程,计算了相分离液体在玻璃转变过程中的结构和动力学特征.研究发现,外压会促进相分离的产生,并提高玻璃转变温度,会使β弛豫出现的温度更高、存在的时间更长,导致系统扩散性降低.同时还发现,相分离液体的玻璃转变过程存在微观不均匀现象. 关键词： 相分离 玻璃转变 分子动力学模拟 外压影响     

精确计算非旋波近似下二能级系统的能谱和动力学性质

利用相干态正交化展开法,精确求解了非旋波近似下Jaynes-Cummings模型的能谱和动力学性质.与近似下解析解比较发现,在弱耦合和强耦合区近似解析解与数值精确解符合很好,但在中间耦合区符合较差. 关键词： 相干态正交化展开 非旋波近似 Jaynes-Cummings模型     

藏红T在阴离子表面活性剂十二烷基硫酸钠上的Langmuir吸附研究

微相吸附 -光谱修正 (MPASC)技术研究了十二烷基硫酸钠 (SLS)与藏红 T(ST)的结合反应 ,分析表面活性剂在微量分析中的增效机理。结果表明 :ST- SLS间相互作用符合 Langmuir单分子层吸附机理 ,产物结合比约为 1∶ 1。     

去甲万古霉素键合手性固定相的制备及其对磷酸苯并哌啉对映异构体的拆分

制备了去甲万古霉素键合手性固定相以及由苯基异氰酸酯衍生化去甲万古霉素键合手性固定相,并在极性有机相模式下对磷酸苯并哌啉进行了手性拆分的研究。发现在此模式下,衍生化去甲万古霉素键合手性固定相对磷酸苯并哌啉的手性选择性要优于没有衍生的去甲万古霉素键合手性固定相;在衍生化去甲万古霉素键合手性固定相上详细考察了流动相组成、酸碱添加剂用量、温度以及流速对分离的影响,优化了分离的条件。在优化的实验条件下,磷酸苯并哌啉可获得基线分离。     

Selective Benzylic and Allylic Alkylation of Protic Nucleophiles with Sulfonamides through Double Lewis Acid Catalyzed Cleavage of sp3 Carbon–Nitrogen Bonds

The acid‐catalyzed benzylic and allylic alkylation of protic nucleophiles is fundamentally important for the formation of carbon? carbon and carbon? heteroatom bonds, and it is a formidable challenge for benzylic and allylic amine derivatives to be used as the alkylating agents. Herein we report a highly efficient benzylic and allylic alkylation of protic carbon and sulfur nucleophiles with sulfonamides through double Lewis acid catalyzed cleavage of sp³ carbon–nitrogen bonds at room temperature. In the presence of a catalytic amount of inexpensive ZnCl₂‐TMSCl (TMSCl: chlorotrimethylsilane), 1,3‐diketones, β‐keto esters, β‐keto amides, malononitrile, aromatic compounds, thiols, and thioacetic acid can couple with a broad range of tosyl‐activated benzylic and allylic amines to give diversely functionalized products in good to excellent yields and with high regioselectivity. Furthermore, the cross‐coupling reaction of 1,3‐dicarbonyl compounds with benzylic propargylic amine derivatives has been successfully applied to the one‐step synthesis of polysubstituted furans and benzofurans.