硫酸高铈铵分光光度法测定葡萄籽提取物中原花青素

建立了葡萄籽提取物中原花青素测定的新方法 硫酸高铈铵分光光度法。它是基于原花青素与Ce4 在强酸性介质中反应生成无色的Ce3 ,通过测定黄色高铈盐的吸光度,间接测定原花青素,Ce4 在319nm波长处具有最大吸收。该方法的线性范围为0.12～10μg mL,RSD为0.98%～1.1%,回收率为97.2%～102.8%,相关系数r=0.9992,检出限为0.04μg mL。     

钇,铈对低铪镍基K444返回合金组织与力学性能的影响

研究了Y,Ce对含铪(Hf)镍基铸造高温合金K444返回料(添加50%返回料)合金的力学性能和组织的影响.研究结果表明:适量Y,Ce(Y<0.03%,Ce<0.015%(质量分数))添加到返回料合金后,一方面,Y,Ce具有去除N,O等有害杂质的作用,使O含量由15×10~(-6)降低到8×10~(-6),N含量由35×10~(-6)降低到18×10~(-6),从而使返回料合金得到净化.另一方面,Y,Ce细化了枝晶组织,减少了共晶和大块状碳化物数量,并且强化了晶界.和未加Y,Ce的返回料合金相比.添加Y,Ce使返回料合金室温拉伸强度提高约100 MPa,塑性提高近一倍;使900℃的高温瞬时拉伸性能波动较为平稳,塑性提高近一倍.添加Y,Ce还可以提高返回合金900℃/274 MPa条件下的持久性能,达到新料水平;可以明显延长K444返回合金900℃/274 MPa条件下的蠕变第二阶段,提高蠕变寿命.     

Oxidase‐Like Activity of Polymer‐Coated Cerium Oxide Nanoparticles

Inorganic enzyme? Ceria nanoparticles exhibit unique oxidase‐like activity at acidic pH values. These redox catalysts can be used in immunoassays (ELISA) when modified with targeting ligands (see picture; light blue and yellow structures are nanoparticles with attached ligands). This modification allows both for binding and for detection by the catalytic oxidation of sensitive colorimetric dyes (e.g. TMB).

     

Electrospun cerium nitrate/polymer composite fibres: synthesis, characterization and fibre-division model

Cerium (Ⅲ) nitrate/poly(vinylpyrrolidone) (Ce(NO3)3/PVP) composite fibres have been prepared by electrospinning. After calcining the composite fibres in air at 500℃,CeO2 nanowires were obtained. The characterizations of the as-spun composite fibres and resultant nanowires have been carried out by a scanning electron microscope (SEM),an infrared spectrometer,an x-ray diffractometer and a fluorescence spectrophotometer. Interestingly,some unusual ribbon-like or twin fibres were observed besides the common fibres with circular or elliptic cross sections. We developed a fibre-division model resulting from Coulomb repulsion and solvent vaporization to interpret the formation of the ribbons or twin fibres,which has been confirmed by the SEM studies. Our results also indicate that the formation of the ribbons or twin fibres is less dependent on operation voltage and work distance.     

同轴静电纺丝技术制备ZnO@CeO2纳米电缆

采用同轴静电纺丝技术,以硝酸铈、硝酸锌、聚乙烯吡咯烷酮、N,N-二甲基甲酰胺、甘油和氯仿为原料,制备了ZnO@CeO2 同轴纳米电缆。用差热–热重分析、X射线衍射、扫描电镜、透射电镜和能谱仪对样品进行了表征。结果表明,所得到的产物为ZnO@CeO2同轴纳米电缆,以晶态CeO2为壳层,晶态ZnO为芯层,电缆直径约90 nm,芯层直径约60 nm,壳层厚度约15 nm,电缆长度>300 μm,对其形成机理进行了分析。     

Polyaniline-coated cerium oxide nanoparticles as an efficient adsorbent for preconcentration of ultra-trace levels of cadmium (ІІ) followed by electrothermal atomic absorption spectrometry

For the first time, polyaniline-coated cerium oxide nanoparticles were synthesized in alkaline media and applied for preconcentration of ultra-trace levels of cadmium (??) in different real samples followed by electrothermal atomic absorption spectrometry. Cerium oxide nanoparticles were synthesized by a microwave method and modified by polyaniline to produce polyaniline-coated cerium oxide nanoparticles. Fourier-transform infrared spectroscopy and scanning electron microscopy were used to characterize the synthesized adsorbent. To optimize the critical experimental conditions; surface response methodology—Box–Behnken experimental design was used. On the basis of the results, pH 8.4, 10?mg of polyaniline-coated cerium oxide nanoparticles, 14.4?min extraction time, and 4.3?min desorption time were selected as the optimum conditions. Under the optimum conditions the calibration curve of cadmium (??) was linear in the range of 0.02–0.4?ng?mL^?1 with a correlation coefficient of 0.9976. The relative standard deviation based on seven replicate analysis of 0.1?ng?mL^?1 cadmium (??) was 4.2% and limit of detection was 0.005?ng?mL^?1 cadmium (??). The analysis of certified reference material shows very good agreement with the certified value. Finally, the proposed method was applied for the determination of ultra-trace levels of cadmium (??) in different water, rice, and tea samples.     

铈γ→α相变的室温动态特性

通过试样组件尺寸匹配设计的被动围压SHPB实验,获得了99.8%纯铈在1.7GPa静水压内的、包含γ?α相变和逆相变过渡区的室温动态静水压-体应变连续曲线。研究显示:室温铈γ→α相变是具有明显滞后现象的一级相变,而非以往研究认为的体积跃变的一级相变;相变过渡区的静水压范围是0.8~1.3GPa。逆相变过渡区的静水压范围是0.6~1.1GPa;逆相变过渡区的静水压-体应变曲线滞后于相变过渡区的静水压-体应变曲线0.15GPa静水压;在相变和逆相变过渡区内,静水压-体应变曲线按照约4.2GPa体积模量的线性关系演化;演化机制为γ和α两相均匀混合、静水压驱动两相组份转化。基于该演化机制,构建了描述相变前后和相变过程的静水压-体应变响应的三段线性模型。     

Zr的添加对提高NH3选择性催化还原NOx整体式催化剂热稳定性的影响

采用共沉淀的方法制备了CeTiO_x和CeZrTiO_x两种用于NH₃选择性催化还原NO_x的催化剂.两种催化剂在不同的高温条件下进行热老化以考察Zr的添加对CeTiO_x催化剂热稳定性的影响.NH₃-SCR活性数据显示,经过650、750和850 ℃的高温老化处理,Zr改性后的催化剂较CeTiO_x催化剂具有更好的催化活性和N₂选择性.XRD、Raman和H₂-TPR结果表明添加Zr可以阻止Ce物种的烧结并且抑制金红石相TiO₂的生成.催化剂的SEM图像显示Zr的添加可以抑制颗粒随着焙烧温度升高而产生的聚集长大.XPS的Ce3d光谱表明,随着老化温度的提升,CeTiO_x催化剂表面的Ce³⁺/Ce⁴⁺比相对于CeZrTiO_x催化剂下降更加明显.这意味着随着Zr的添加,更多的晶格缺陷和氧空缺出现在Zr改性催化剂的表面,这有利于催化性能的提升.另外,NH₃-TPD结果表明经过相同的高温老化,改性的催化剂保持了更多的Brönsted酸性位,提高了催化活性并抑制了氨的氧化.因此,Zr的添加提高了催化剂的热稳定性能.     

Effect of Mg2+ co‐doping on the scintillation performance of LuAG:Ce ceramics

Ce‐doped Lu₃Al₅O₁₂ optical ceramics co‐doped with Mg²⁺ are fabricated by solid‐state reaction method and further optimized by an air‐annealing process. Mg²⁺ co‐doping leads to a significant decrease of thermoluminescence intensity above room temperature and an increase of scintillation light yield (LY) value and fast component content even if the overall scintillation efficiency decreases. Scintillation LY of ～21900 ph/MeV has been achieved with a short shaping time of 1 μs, and the ratio of LY values for 1 μs and 10 μs shaping times was as high as 79%. The acceleration of scintillation response induced by Mg²⁺ co‐doping and the role of Ce⁴⁺ ions in the scintillation mechanism are discussed.

     

含氮不饱和大环铈配合物催化磷酸二酯降解的研究

本文利用含氮不饱和大环铈配合物催化BNPP水解。通过改变温度、pH等方法测定含氮大环铈配合物催化对硝基苯酚磷酸二酯的反应速率。整个实验过程保持含氮大环铈配合物浓度高于底物浓度10倍以上,以使反应为一级反应。结果表明:其水解反应的最佳温度在45℃左右,最佳pH在8.0左右。