UPLC-ELSD Determination of 1-Octacosanol in Raw Material and Health Products

Determination of the levels of 1-octacosanol is important in food stuff for the study of its pharmacological activities and health benefits. In this study, a novel, simple and fast internal standard method for the non-derivatization ultra-performance liquid chromatographic determination of 1-octacosanol in raw materials and health products was developed and validated based on evaporative light scattering detection. The linearity (r ² > 0.998), recovery (99.1–100.2%, RSD <2.7%), intra- and inter-day precision (RSD <3.8%), limit of detection (1.0 mg/L), limit of quantification (2.2 mg/L) of the 1-octacosanol were determined. The method was successfully applied to nine real 1-octacosanol products. The results of analyses had close agreement with the labeled claims of 1-octacosanol content in these products. Compared with the classical gas chromatography method, the developed method was simpler, faster and more environmentally friendly due to avoiding any derivatization step. This protocol represents a rapid and feasible method for quality control of 1-octacosanol products.

     

Synthesis of mikto‐topology star polymer containing one cyclic arm

Well‐defined mikto‐topology star polystyrene composed of one cyclic arm and four linear arms was synthesized by a combination of atom transfer radical polymerization (ATRP) and Cu‐catalyzed azide‐alkyne cycloaddition (CuAAC) click reaction. First, the bromine‐alkyne α,ω‐linear polystyrenes containing four hydroxyl groups protected with acetone‐based ketal groups were synthesized by ATRP of styrene using a designed initiator. Then, the bromine end‐group was converted to the azide and the linear polystyrene was cyclized intra‐molecularly by the CuAAC reaction. The four hydroxyl groups were released by deprotection and then esterified with 2‐bromoisobutyryl bromide to produce a cyclic polymer bearing four ATRP initiating units. By subsequent ATRP of styrene to grow linear polymers with the cyclic polystyrene as a macroinitiator, the mikto‐topology star polymers were prepared. © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2012     

低温生长Cu(InGa)Se2薄膜吸收层的掺钠工艺研究

在柔性聚酰亚胺衬底上低温制备Cu(In,Ga)Se₂薄膜太阳能电池, Na的掺入会改善电池特性, 但不同的掺Na工艺对Cu(In,Ga)Se₂薄膜和器件特性的改善机理不同. 本实验通过对比前掺NaF和后掺NaF工艺发现, 在前掺Na工艺下, 由于Na始终存在于Cu(In,Ga)Se₂薄膜生长过程中, Na存在于多晶 Cu(In,Ga)Se₂ 薄膜晶界处, 起到了扩散势垒的作用, 导致晶粒细碎、加剧两相分离, 同时减小了施主缺陷的形成概率; 而在后掺Na工艺下, 掺入的Na对薄膜的结构及生长不产生影响, 仅仅起到了钝化施主缺陷、改善薄膜缺陷态的作用. 同时, 研究表明, 后掺Na工艺中, NaF必须依靠外界能量辅助才能扩散进Cu(In,Ga)Se₂内部, 实验结果证实, 只有衬底温度达到350 ℃以上时, 掺入的NaF才能较好地改善薄膜特性. 最终经掺Na工艺的优化, 得到低温工艺制备的柔性聚酰亚胺衬底器件效率达10.4%.     

超软X射线流气式正比计数管

介绍了一种用于测量183～933eV超软X射线的圆柱形、侧窗式、流气式正比计数管,工作气体是0.11MPa的P-10气体或氦气-丙烷混合气体。计数管内径为φ25mm,直径为φ0.3mm的入射窗是由厚度80～90μgcm~2聚乙烯甲醛制成的。该计数管的特点:(1)薄窗,对软X射线透过率高。(2)流气式,工作寿命长。(3)能量分辨率好。(4)计数率高(1×10~(14)个/s)。(5)可测能区宽(0.183～10keV)。(6)可以方便更换窗膜材料、厚度及窗口直径。近几年来该计数管已经为高强度低能X光源提供较好监测。     

256色模式下图形图像处理系统中对不规则区域的处理

概述了图形图像处理系统中关于不规则区域的基本算法，包括：区域填充，边界跟踪，边界标志，几何处理，区域分割等等．并且，根据２５６色模式的特殊性，对传统的算法做了有针对性的改进，加快了处理速度，使其更适合于电影电视字幕、动画卡通人物等不规则图形图像区域．同时还给出了改进算法的程序设计的技巧．     

考虑处置效果的苯系物泄露应急方案生成方法

针对苯系物泄露次生突发环境事件的应急响应问题,研究了基于案例推理和处置效果的应急方案生成方法。首先,在计算案例相似度时,为避免历史案例不全产生的情景要素遗失,基于随机森林算法,结合专家知识构建了权重求解方法,采用案例检索方法得到相似案例集;然后,构建了应急处置效果评估指标体系,以全面评价相似案例对应的处置效果;进一步,考虑多专家评价可弥补决策者知识、经验等的不足,引入了自适应群共识调整算法,得到群体评价意见,通过集结相似度与处置效果,得到了方案的综合评价值并生成最优方案;最后,用算例说明了方法的可行性和有效性。     

C60在几种溶剂中紫外吸光度的负热效应

所采用的变温光谱差减方法是将待测试样分成两份 ,一份作为参比试样 ,恒定在某一温度 (参比温度 )下 ,另一份作为待测样品 ,选定另一待观测温度 ,在一定的波长范围内 ,用岛津UV 2 4 0型紫外 可见双光束分光光度计扫描 ,获得紫外吸收温差光谱 (UVSDT)。选择不同的温度差 ,测得温差光谱随温差的变化。观测了C60 分子在乙醇、环己烷、正己烷、异丙醇等几种有机溶剂中吸光度随温度的变化。观测结果发现C60 溶液的吸光度变化存在显著的负温度效应。C60 的UV吸收光谱峰随试样温度升高而降低 ,UV吸收温差光谱 (U VSDT)为负峰 ,UVSDT峰强随温差增大而负向增大。说明C60 的结构对温度有较强的依赖关系。这种依赖关系与π π 电子跃迁类型密切相关。实时现场测量C60 溶液的吸光度随温度变化规律 ,对分离、纯化、分析富勒烯 ,认识C60 特性、研究以溶剂为媒介的化学反应机理 ,以及提高测量的准确度和重现性等 ,均有一定的理论意义和实用价值