纳氏试剂分光光度法测定铝灰渣浸出液中的氨氮含量

随着水土资源环境日益恶化,监测氨氮量对水土的污染程度也备受关注。为了准确测定铝灰渣浸出液中的氨氮量,实验对振荡方法、振荡时间、固液比、试液过滤方式、纳氏试剂加入量以及测定干扰因素进行了研究。确定了以翻转振荡为前处理方式,最佳振荡时间为14 h,固液比为1:10,最佳纳氏试剂加入量为1.0 mL,通过改善过滤方式,降低了空白值。由实验结果可知：在试验范围内,F^-对氨氮量的测定不产生干扰;对于浸出液中Cl^-、Al³⁺和Ca²⁺浓度高的样品,可通过移取稀释液2.00 mL,加入1.0 mL酒石酸钾钠溶液(500 g/L),即可消除其干扰。运用纳氏试剂分光光度法测定铝灰渣浸出液中的氨氮量,得到氨氮标准曲线线性相关系数为0.9998,方法检出限为0.39 mg.L^-1,RSD(n=6)<5%,回收率在94.7%～105%之间。本方法简单快速,精密度高,且具有较低的检出限,适用于大批量铝灰铝渣等固体废物浸出液中氨氮量的测定。     

介孔钯-硼合金纳米颗粒的制备和甲醇氧化电催化性能北大核心CSCD

合金化可以调节贵金属纳米材料的物理化学性质,从而显著提升它们的电催化性能。尽管合金化在过去的20多年里已取得诸多成果,但是如何充分发挥纳米合金的组分优势仍需深入的探究。本研究通过一步溶液相合成法实现了类金属硼(B)合金化的钯基介孔纳米催化剂材料的合成,同时探究了B原子的组分优势和介孔形貌的结构优势在碱性介质中电化学甲醇氧化反应(MOR)的协同作用。最优PdCuB介孔纳米催化剂表现出优异的电化学MOR活性和稳定性。机理研究表明,优异的催化活性源于B原子在Pd基介孔纳米催化剂中的积极协同作用;该协同作用通过电子效应(改变Pd的表面电子结构从而减弱CO基中间体的吸附)和双功能效应(促进OH_(2)的吸附从而氧化CO基中间体)在动力学上加速了有毒CO基中间体的去除(提高甲醇氧化的决速步骤)。同时,B原子的间隙插入和介孔结构抑制了物理奥斯特瓦尔德(Ostwald)熟化过程,显著增加了催化剂的稳定性。     

基于语义相似度与XGBoost算法的英语作文智能评价框架研究

作文智能评分和评语智能生成能极大减轻评阅专家的工作量、节约人力成本。目前，评分和评语结果的准确性与公平性尚不高。近年来，机器学习和自然语言处理等技术的快速发展，在一定程度上提升了文本分类、机器翻译等任务的性能，但仍有许多新的研究成果尚未应用于作文智能评价。本研究综合了词向量(word2vec)、段落向量(paragraph2vec)、词性向量(pos2vec)和LDA (latent dirichlet allocation)等特征，共同组合为作文的语义表示向量；采用基于kNN (k nearest neighbors)算法的语义相似度模型，得到作文的评语标签；采用基于XGBoost(extreme gradient boosting)的回归模型计算英语作文的评分值；并以900篇大学生英语作文为样本，构造算例进行验证。最后表明，提出的智能评价框架在英语作文自动评分和评语生成的准确性上，都要高于传统方法。     

基于介孔二氧化硅包载白藜芦醇纳米体系的制备

本实验旨在构建一种介孔二氧化硅包载白藜芦醇的纳米体系,并通过扫描电子显微镜、透射电子显微镜、X射线衍射、N₂ 吸附-脱附、差热-热重分析等对包载白藜芦醇前后的纳米体系进行表征分析,探究其光、热稳定特性和体外不同pH 值缓冲液中的释放规律。结果表明,制备的介孔二氧化硅包载白藜芦醇纳米体系,其骨架呈交联网络结构,孔径、比表面积和孔容分别为10.16 nm、245.73 m²/g和0.79 cm³/g,负载量可达39.44%,且负载后其骨架结构未破坏,并有效提高了白藜芦醇的光、热稳定性。同时,经过纳米体系负载后的白藜芦醇2 h内释放速率在两种不同pH 值缓冲液中均可达80%以上。介孔二氧化硅包载白藜芦醇纳米体系性能较好,为白藜芦醇的进一步开发利用提供参考。     

菜粉蝶颗粒体病毒包涵体在银胶中的表面增强拉曼光谱研究

本文讨论了菜粉蝶(preris rtpae)颗粒体病毒(简称 PrGV )包涵体在银胶中的表面增强拉曼光谱。PrGV 包涵体的 SERS 谱与其 RS 谱之间存在一定对应关系。PrGV 包涵体蛋白分子通过羧基和氨基基团吸附于银粒子表面,并构成阴离子形式(NU_2RCOO~-)存在于溶液中。PrGV 在银胶中的表面增强的增强机制属于短程作用。PrGV 包涵体与银胶表面的吸附主要是化学吸附。     

剪切壁流有旁支管道及一小球时的流动计算

本文研究了旁支管道附近的剪切流场变化；计算时考虑到小球的存在．本文采用了《有限元程序自动生成系统》，整个计算所用工作量极少．     

Investigation on optical transmission spectra of (1−x)Pb(Mg1/3Nb2/3)O3-xPbTiO3 single crystals

The optical transmission spectra from 0.3 to 11 μm of relaxor ferroelectric single crystals (1−x)Pb(Mg_1/3Nb_2/3)O₃-xPbTiO₃ (PMN-xPT) were systematically studied at room temperature in this paper. The crystal is transparent between 0.45 and 5.5 μm and becomes completely absorbing around 0.4 μm in near UV region and 10 μm in infrared region. But the wavelength cutoff in near UV is much sharper than the long wavelength cutoff. As compared with other configurations, tetragonal single crystals possess the optimal transmission properties. The optical transmittance in the wavelength region from 0.45 to 5.5 μm is about 70%. The results show that tetragonal PMN-xPT single crystals are promising for a wide range of optical applications. Some discussions about the oxygen-octahedra structure that determines the basic energy level of the crystals are also presented on the optical properties of PMN-xPT single crystals.     

Electro-optic characterization of tetragonal (1−x)Pb(Mg1/3Nb2/3)O3-xPbTiO3 single crystals by a modified Sénarmont setup

The refractive indices of tetragonal (1−x)Pb(Mg_1/3Nb_2/3)O₃-xPbTiO₃ (PMN-xPT) single crystals were measured with a prism coupler and their linear electro-optic (EO) properties were investigated from 20 to 80 °C by the automated scanning Sénarmont system with an ac field. The composition and temperature effect on the EO coefficients were also discussed. It has been found that their EO coefficients are much larger than that of widely used LiNbO₃ single crystal and the calculated half-wave voltages are also much lower, which enable the operation at lower voltages and the smaller device dimensions. Since the excellent EO properties are very stable and such high quality single crystals with large-size have been obtained, the PMN-xPT single crystals are a very promising candidate for EO modulation applications. By linking to the polarization-related quadratic EO coefficients, we find that the linear EO properties are related with the spontaneous polarization and dielectric constants.     

Efficient Detection of Environmental Estrogens Bisphenol A and Estradiol By Sensing System Based on AuNP-AuNP-UCNP Triple Structure

A sensing system based on AuNP-AuNP-UCNP triple structure for efficient detection of dual targets bisphenol A and estradiol was constructed. In the preparation of triple structure, the gold nanoparticles (AuNPs) and upconversion nanoparticles (NaYF₄: Yb, Er, Gd, UCNPs) were synthesized and surface modified. Then, the two nanoparticles and their aptamers were connected to form two kinds of optical fluorescent probes. A nucleic acid sequence that matches with two aptamers was designed, rendering the probes to get close based on the principle of complementary base pairing. On the basis of this, a sensing system with triple structure was prepared, and its connecting effect was characterized by TEM. With this system, dual targets of bisphenol A and estradiol were detected efficiently and conveniently through quantitatively determination by fluorescence and UV spectrophotometer. At the reaction temperature 30 °C and pH 7.8, this method exhibited good linear range for determination of bisphenol A and estradiol from 2 ng mL^–1 to 200 ng mL^–1 and from 10 ng mL^–1 to 150 ng mL^–1, with the limits of detection of 0.2 ng mL^–1 and 0.5 ng mL^–1, respectively. This sensing system with triple structure owned better specificity to structural and functional analogues, showed good repeatability and stability. What's more, this sensing system could be applied to actual water detection, with the recoveries of 86.1%–107.4%, and the relative standard deviation below 6.8%. This method shows promising applications in other environmental estrogens in water sample.     

A comparative study on in vitro cytotoxicity,cellular uptake,localization and apoptosis-inducing mechanism of two ruthenium(II) complexes

Two ruthenium complexes [Ru(MeIm)₄(bpy)]²⁺ (Ru1, MeIm = 1-methylimidazole, bpy = 2,2′-bipyridine) and [Ru(Im)₄(bpy)]²⁺ (Ru2, Im = imidazole) with the same PF ₆ ^? counter-ion but different lipophilicities were synthesized and characterized and as potent anticancer agents. The relationships between cellular uptake, localization and molecular action mechanisms of these complexes were elucidated. The results showed that Ru1 with higher logP_o/w exhibited faster cellular uptake rates, but lower anticancer activity than Ru2. In addition, Ru1 predominantly accumulated in the mitochondria and cytoplasm, and induced G0/G1 cell cycle arrest, whereas the more hydrophilic Ru2 tended to localize and accumulate in the cell nucleus and mitochondria. Further mechanism studies indicated that Ru2 caused cell cycle arrest at S phase by regulating cell cycle related proteins and induced apoptosis in A549 cells through DNA damage, cellular ROS accumulation, activation of the caspase pathway and mitochondrial dysfunction.