多种优化试剂显现潮湿纸张表面潜在手印的比较研究

复杂条件下潜在手印的发现及显现提取一直以来是刑事技术领域研究的热点和难点,尤其是潮湿或水中浸泡客体表面的潜在手印,往往因为环境条件的影响而无法使用常规的显现方法。因此,对于这类疑难条件下潜在手印的显现研究成为亟待解决的问题。本文分别对比了尼罗红、尼罗蓝、物理显影液三种可用于潮湿客体表面潜在手印显现的优化试剂,并对其可靠性、灵敏度及使用条件进行了详细的论证分析,为实战工作中疑难条件下潜在手印的显现提出了可靠的处理方法。     

中学化学骨干教师PCK的实证研究*——以“析氢腐蚀和吸氧腐蚀”主题为例

使用本土化的教学内容表征(CoRe)工具调查了46名接受“国培计划”的中学化学骨干教师关于“析氢腐蚀和吸氧腐蚀”主题的PCK,结果表明:(1)骨干教师的PCK包含5个相互联系的组分,其中课程知识、学生知识以及策略知识均较为丰富。骨干教师能有针对性地选取化学学科专属的教学策略;(2)在教学取向方面,骨干教师在教学中发展与评价学生化学基本观念与学科核心素养的意识有待加强,引导学生自主建构学习的落实程度有待提高;(3)在评价知识方面,评价方式较为多元,但骨干教师对于形成性评价的重视程度不够。文末据此对我国化学教师教育以及化学PCK研究提出相关建议。     

固相萃取/气相色谱-质谱法对土壤中有机氯农药的分析及基质效应研究

建立了一种固相萃取/气相色谱-质谱法同时测定土壤中23种有机氯农药的方法,并研究了不同基质效应补偿方式。土壤样品经正己烷∶丙酮(体积比1∶1)提取,弗罗里土小柱净化,采用气相色谱-质谱仪检测。结果发现7种有机氯存在中/强程度的基质效应;在10 mL二氯甲烷∶正己烷(体积比1∶9)+10 mL丙酮∶正己烷(体积比1∶9)为固相萃取的洗脱剂,且脉冲压力为275.8 kPa条件下,可将23种有机氯的基质效应均控制在20%以内。23种有机氯农药在0.4～10μg·mL~(-1)质量浓度范围内线性良好,相关系数(r~2)均不小于0.999 2,检出限为1.0～8.6μg·kg~(-1),定量下限为4.0～34.4μg·kg~(-1);在20、60、100μg·kg~(-1)3个加标水平下空白土壤中的平均回收率为46.3%～127%,相对标准偏差(n=6)为0.68%～15%。采用该方法在某土壤样品中检出α-六六六、γ-六六六、p,p′-DDE、异狄氏剂醛、p,p′-DDT 5种有机氯农药。     

高效液相色谱-四极杆/飞行时间高分辨质谱测定化妆品中的西咪替丁及雷尼替丁

建立了化妆品中西咪替丁及雷尼替丁的高效液相色谱-四极杆/飞行时间高分辨质谱检测方法,并对其质谱裂解规律进行研究。待测样品经甲醇超声提取,过滤膜后经Zorbax SB-Aq色谱柱(3.0 mm×100 mm,1.8μm)分离,用乙腈-含0.1%甲酸的水溶液梯度洗脱后,在双喷雾电喷雾离子源正离子模式下检测,数据采集使用一级母离子全扫描和目标二级离子扫描。在不同的化妆品基质中,西咪替丁和雷尼替丁分别在5.65～113 ng/mL和4.95～99.0 ng/mL范围内线性关系良好(r0.999),检出限分别为1.1、0.99 ng/mL,定量下限分别为5.6、5.0 ng/mL;2种待测物在低、中、高3个加标水平下的回收率为86.7%～110%,相对标准偏差(RSD)为0.90%～6.0%,方法重复性良好(RSD10%)。该方法前处理简单,灵敏度较好,线性、回收率及重复性均满足方法学要求,可用于化妆品中西咪替丁和雷尼替丁的筛查测定。     

同位素稀释高效液相色谱-串联质谱法测定水体、底泥、鱼及虾中氯硝柳胺残留量

建立了水体、底泥、鱼体自然比例带皮肌肉和虾肌肉中氯硝柳胺(NIC)残留量测定的同位素稀释高效液相色谱-串联质谱(HPLC-MS/MS)法。水样经碱化后以乙酸乙酯提取,其他样品采用0.1%氨水乙腈提取,C_(18)粉进行样品净化。以乙腈-水为流动相,流速为0.3 mL/min,采用Thermo Hypersil Gold C_(18)(150 mm×2.1 mm,5μm)色谱柱进行分离,氯硝柳胺稳定同位素标记物(氯硝柳胺-~(13)C_6)为内标,选择反应监测(SRM)模式扫描,内标法定量。结果表明氯硝柳胺在0.2～200μg/L范围内呈良好线性关系,相关系数(r~2)不小于0.999 5。空白水样在2.5、25、250 ng/L加标水平下的平均回收率为90.5%～109%,相对标准偏差(RSD)为3.2%～11%,检出限(LOD)为1.0 ng/L,定量下限(LOQ)为2.5 ng/L;空白底泥、黄颡鱼自然比例带皮肌肉和克氏原螯虾肌肉在0.5、5.0、50μg/kg加标水平下的平均回收率分别为89.4%～113%、92.8%～110%和94.1%～107%,RSD分别为4.6%～12%、2.8%～11%和3.2%～9.3%,LOD均为0.2μg/kg,LOQ均为0.5μg/kg。该方法的灵敏度、准确度和选择性高,适用于实际水产养殖环境水体、底泥、鱼和虾中氯硝柳胺的残留分析。     

Recent Progress on 2D Transition Metal Compounds-based Electrocatalysts for Efficient Nitrogen Reduction

Ammonia is a commodity chemical with high added value. Electrochemical reduction of nitrogen has great promise for the sustainable synthesis of ammonia in recent years. Because of its rich resources and unique electronic structure and characteristics, 2D transition metal compounds have been used as electrocatalysts for electrochemical reduction of nitrogen for clean and sustainable production of ammonia. This review outlines the latest development in the use of 2D transition metal compounds as high-efficiency electrocatalysts for nitrogen reduction reaction(NRR). First, we introduce the N₂ reduction mechanism, and briefly summarize the performance indicators of the catalyst. Then, we focused on the functionalization of unique 2D materials to design high-performance 2D electrocatalysts in respect of simulation calculation and experimental development. Finally, the current challenges and future opportunities for NRR electrocatalysts are introduced.     

Recent Advances in Atomic-scale Storage Mechanism Studies of Two-dimensional Nanomaterials for Rechargeable Batteries Beyond Li-ion

Developing new types of rechargeable batteries with high energy densities and low cost have received increasing attentions, aiming to reduce the dependence on high-priced lithium. Beyond Li-ion batteries, the potential alternatives including Na-ion batteries, Li-S batteries and Li-air batteries have been investigated recently, which are required to be viable for commercial applications. From this point of view, to understand the electrochemical reaction mechanisms and kinetics of these batteries has become the key challenge to make breakthroughs in the field of new energy storage. In this review, we present a critical overview of the two dimensional nanomaterials-based batteries (except Li-ion-based batteries) that could meet such demonds. To develop new energy storage devices with more promising performances, the microstructure evolution and atomic scale storage mechanism of these batteries are comprehensively summarized. In addition, the major challenges and opportunities of advanced characterization techniques are finally discussed. We do hope that this review will give the readers a clear and profound understanding of the electrochemical reaction mechanisms and kinetics of the as-discussed batteries, thus effectively contributing to the smart design of future-generation energy storage devices.     

Synthesis of N-TiO2@NH2-MIL-88(Fe) Core-shell Structure for Efficient Fenton Effect Assisted Methylene Blue Degradation Under Visible Light

Core-shell TiO₂-based photocatalysts with specific composition, morphology, and functionality have attracted considerable attention for their excellent degradation properties on organic pollutants via a photocatalytic oxidation process. Herein, a N-TiO₂@NH₂-MIL-88(Fe) core-shell structure was prepared by coating NH₂-MIL-88(Fe) on nitrogen-doped TiO₂(N-TiO₂) nanoparticles. Introduction of heteroatom nitrogen to pure TiO₂ expands the spectral response range, leading to enhanced quantum efficiency of photocatalyst. Furthermore, loading NH₂-MIL-88(Fe) on N-TiO₂ improved the adsorption ability of the nanocomposites due to the porous tunnels of NH₂-MIL-88(Fe). The resulted core-shell N-TiO₂@NH₂-MIL-88(Fe) nanocomposites realized the transfer of photo excited electrons from N-TiO₂ to NH₂-MIL-88(Fe) rapidly, partially reduced Fe³⁺ to Fe²⁺ in NH₂-MIL-88(Fe), and further enhanced the Fenton effect on efficiently degrading methylene blue dye(MB) under visible light(λ ≥ 420 nm) with the assistance of H₂O₂.     

单晶电极界面反应过程的电化学原位拉曼光谱研究

自20世纪70年代起,人们利用原位光谱技术（拉曼、红外等）对电化学界面进行了系统的研究,进而发展出原位谱学电化学的研究方向,由于其具有良好的表面灵敏度和能量分辨率,可以提供更多的表面反应信息,进而从微观上揭示反应机理. 伴随着纳米技术的兴起,表面增强拉曼光谱技术取得了快速的发展. 近来,壳层隔绝纳米粒子增强拉曼光谱（shell-isolated nanoparticle-enhanced Raman spectroscopy,SHINERS）技术更是得到人们的广泛关注. SHINERS的出现为研究单晶模型电极上的催化反应提供了一种非常好的原位光谱技术. 本文主要对原位电化学SHINERS技术在单晶电极界面研究的具体应用及其发展前景进行相关论述.     

对硝基甲苯合成3,4-二甲基苯胺的研究

以对硝基甲苯为原料,经胺甲基化、水解、还原3步反应合成了目标化合物。通过单因素实验,分析每一步反应的关键影响因素,初步得到适宜的合成条件。最终产物的结构经核磁氢谱、质谱、元素分析进行确证,纯度经气相色谱分析。3,4-二甲基苯胺的总收率56.6%,纯度大于98.5%。该合成路线原料易得,成本较低,操作简单。