六方相磷酸铈一维纳米材料的合成与表征

以磷酸钠、硝酸铈为原料, 利用P123表面活性剂的水溶液形成的胶束为反应模板, 采用水热法合成工艺, 在反应溶液的pH＝1, 反应温度为140 ℃, 反应时间为24 h的条件下成功合成了六方相的CePO4一维纳米发光材料, 并提出其可能的形成机理. 通过XRD, TEM, FT-IR, UV-Vis, PL测试表征, 发现制备的磷酸铈一维纳米材料最长可以达到1 μm左右, 而直径为10～25 nm, 轴径比较高; 其在紫外光区的荧光发射性能与普通的纳米颗粒相比得到了很大程度的提高; 六方相磷酸铈一维纳米材料以其独特的荧光发射性能, 有望在光、电等领域发挥其潜在的应用价值.     

界面聚合及其应用进展

综述了界面聚合的发展过程及其在膜、微胶囊、纳米材料、聚酯等制备方面的应用进展.     

功能化PbS量子点的水相合成及结构表征

在水溶液中以Pb(NO3)2和Na2S为原料,巯基乙酸为稳定剂,合成了水溶性PbS量子点.用透射电子显微镜、扫描电子显微镜、粒度分析仪和红外光谱对PbS量子点进行了表征,结果表明所合成的PbS量子点的平均粒径为25 nm左右,分散性好,且巯基乙酸成功修饰于PbS纳米粒子表面,使其具有进一步与生物分子偶联的作用.     

Automation and Standardization—A Coupled Approach towards Reproducible Sample Preparation Protocols for Nanomaterial Analysis

Whereas the characterization of nanomaterials using different analytical techniques is often highly automated and standardized, the sample preparation that precedes it causes a bottleneck in nanomaterial analysis as it is performed manually. Usually, this pretreatment depends on the skills and experience of the analysts. Furthermore, adequate reporting of the sample preparation is often missing. In this overview, some solutions for techniques widely used in nano-analytics to overcome this problem are discussed. Two examples of sample preparation optimization by automation are presented, which demonstrate that this approach is leading to increased analytical confidence. Our first example is motivated by the need to exclude human bias and focuses on the development of automation in sample introduction. To this end, a robotic system has been developed, which can prepare stable and homogeneous nanomaterial suspensions amenable to a variety of well-established analytical methods, such as dynamic light scattering (DLS), small-angle X-ray scattering (SAXS), field-flow fractionation (FFF) or single-particle inductively coupled mass spectrometry (sp-ICP-MS). Our second example addresses biological samples, such as cells exposed to nanomaterials, which are still challenging for reliable analysis. An air–liquid interface has been developed for the exposure of biological samples to nanomaterial-containing aerosols. The system exposes transmission electron microscopy (TEM) grids under reproducible conditions, whilst also allowing characterization of aerosol composition with mass spectrometry. Such an approach enables correlative measurements combining biological with physicochemical analysis. These case studies demonstrate that standardization and automation of sample preparation setups, combined with appropriate measurement processes and data reduction are crucial steps towards more reliable and reproducible data.     

有机纳米材料的应用及分析方法研究进展

有机纳米材料是指基于脂质、蛋白、多糖及有机高分子聚合物的新型纳米材料。近年来,随着纳米科技的发展,有机纳米材料已被广泛应用于食品、农业、生物医药等行业中。虽然有机纳米材料独特的性质使其具有很大的应用潜力,但同时也存在潜在的健康风险。一些难降解的有机纳米粒子能够通过人类活动被排入环境中,并在生物体中不断累积。因此,有机纳米材料的安全性研究日益受到重视,对其分析表征方法也提出了新的要求。目前对有机纳米材料的分析主要包括样品处理、分离、表征、检测等步骤,其中主要涉及过滤、离心、电镜、色谱、光谱、质谱等技术。该文综述了目前有机纳米材料的应用及其分析方法的研究进展,并对未来研究趋势进行了展望。     

固相萃取材料在金属离子前处理应用中的研究进展

为避免摄入过量重金属、危害人类健康,应提高对金属离子的检测能力.常用的金属检测技术如电感耦合等离子体质谱、电热原子吸收光谱、火焰原子吸收光谱等可以有效识别痕量重金属,并且具有多组分分析能力以及检出限低、产量高等优点.但复杂样品本身浓度较低且基质干扰大,因此检测前需进行前处理以消除基质干扰,满足低浓度和小体积样品的检测需...     

固定Fe 3＋的磁性微球分离富集鼠肝中铁结合蛋白的初步研究

采用键合Fe3＋的纳米材料分离富集了大鼠肝脏中的铁结合蛋白质组, 并进行了质谱分析. 在相同的起始富集蛋白质量以及相同的吸附和洗脱条件下, 键合了Fe3＋的磁性纳米材料比未键合金属离子的空白材料富集了更多的蛋白质, 经质谱鉴定得到42个蛋白质, 主要包括代谢酶类、呼吸链主要成员、氧化还原蛋白、转运蛋白、血红蛋白等.     

共价有机框架的合成及其在肿瘤治疗中的应用研究进展

共价有机框架(covalent organic frameworks,COFs)是近年来开发的一种由有机单元连接而成的高结晶性多孔聚合物,由于具有良好的孔隙率、模块性、结晶性和生物相容性等特点在肿瘤治疗中显示出了良好的应用前景.本综述总结了已报道的COFs制备方法,包括溶剂热合成法、机械化学合成法、微波合成法、离子热合...     

新型空间硅太阳电池纳米减反射膜系的优化设计

结合纳米材料折射率（小于1.4）和AM0太阳光谱特性,对空间硅太阳电池的减反射膜进行了设计分析.分别设计了常规材料和纳米材料的双层、三层减反射膜,得到了最佳的膜系参数,并作出了反射率变化曲线.结果发现,采用低折射率纳米材料的三层减反射膜有着更好的减反射效果,新型纳米减反射膜系与采用常规材料的减反射膜系相比,优化后的最小加权平均反射率减小了15%（双层减反射膜）和24.5%（三层减反射膜）. 关键词： 折射率 减反射膜 纳米材料 空间硅太阳电池     

Gas-Constructed Vesicles with Gas-Moldable Membrane Architectures

Integrating gas as a main building block into nanomaterial construction is a challenging mission that remains elusive. Herein, we report a gas-constructed vesicular system formed by CO₂ gas and frustrated Lewis pairs (FLPs). Two molecular triads bearing three bulky borane and phosphine groups are designed as trivalent disc-like FLP monomers. CO₂, as a gas cross-linker, can drive the two-dimensional polymerization of these two FLP monomers, leading to the generation of planar FLP networks that further transform into a thermodynamically favored membranous vesicle structure. Gas-guided vesicle formation is also applicable to other inert but FLP-activatable gases. Different gas linkages can form vesicles with distinct architectures, sizes, and morphologies. We envisage that this study would suggest a new concept that exploits gases to fabricate tunable nanomaterials.