Pt-Au二元双金属/氧化石墨烯电化学传感器同时检测尿酸及多巴胺的应用研究

尿酸(UA)是人体最基础的代谢产物,多巴胺(DA)是一种重要的神经递质。二者同时存在于体液当中,其含量对于人体的健康有着极大的影响,因此实现快速、高效、准确的同时检测具有非常重要的意义。该文研制了一种基于Pt-Au二元双金属负载石墨烯的电化学传感器用于尿酸和多巴胺的测定,结果表明Pt-Au和石墨烯的纳米复合物对尿酸和多巴胺具有非常好的催化氧化作用,并且能实现峰的分离(ΔE>200mV),为尿酸和多巴胺的同时测定提供了有力条件。该传感器对尿酸和多巴胺同时测定的检测下限分别为1.996μmol/L和0.999μmol/L,线性范围分别为17.417μmol/L～1259.357μmol/L和2.486μmol/L～260.141μmol/L。基于Pt-Au二元双金属和石墨烯的电化学传感器具有制作简单方便,成本低廉且具有良好的重现性,用于实际样品的同时测定也得到较好的效果。     

"牺牲"阳极法合成乙醇钽研究

研究了“牺牲“阳极法电化学合成乙醇钽过程中,添加剂种类与浓度、电解液温度、阴阳极极距和电流密度的影响.选取最佳合成条件为:四甲基氯化铵0.04 mol/L,温度为电解液的沸腾温度,极距约2 cm,电流密度220 A/m2.电合成的混合液经常压蒸馏和减压蒸馏,得到产品用红外光谱、拉曼光谱和元素分析进行表征,确定了产品为乙醇钽.电合成的电流效率大于95%,产品蒸馏时钽的直收率82.8%.     

银纪念币的腐蚀变色研究

银纪念币在大气环境中表面发生变色，失去原有的金属光泽。采用OM，SEM，EMPA，XPS，XRD等现代物理测试技术对变色的银纪念币进行分析。结果表明，银纪念币的变色部位呈均匀的浅褐色，并随机分布着深褐色的斑点。变色银纪念币表面沿着划痕密集分布着蚀孔。表面分析显示，除Ag外，还有S和O元素。XPS，XRD分析发现，变色银纪念币表面存在Ag2S，Ag2SO3和Ag2O。实验室加速变色试验毒明，在含S气体环境中，Ag被氧化生成A82S，导致银纪念币表面变色,从而验证银纪念币的变色是由电化学腐蚀引起的，S和O元素参与了腐蚀历程。     

电沉积镧镍合金薄膜的电化学贮氢性能研究

利用在水溶液中电沉积的方法制备了LaNi5贮氢合金薄膜。采用XRD方法研究了贮氢合金薄膜在充放电前后相结构的变化，运用扫描电镜观察了合金薄膜的表面形态，通过电化学测试（循环伏安、恒电流充放电）研究其电化学贮氢性能。结果表明，该合金薄膜具有较好的电化学贮氢性能，电化学活性较高，无需活化过程，最高电化学容量可达156mAh／g。     

小间隙电解加工工艺探讨

简要阐明了小间隙电解加工的主要工艺及注意事项.     

Structural stability of single-layered LaNi4.25Al0.75 film and its electrochemical hydrogen-storage properties

AB5-based hydrogen storage thin fdms （LaNi4.25Al0.75）, deposited on Cu substrate by dc magnetron sputtering were investigated in this study. X-ray diffraction （XRD） revealed that the microstructure of the layer was in crystal form. SEM and AFM analyses proved that the film appeared to be rather rough with numerous randomly sized pores of approximately 15-40 in nm diameter. Structural stability of the film was examined by the combined analyses of DSC, XRD, and SEM, which indicated that this film maintained its structural stability below 500 K or so, and a network structure was observed on the film after being heated at 700 K for 30 min. Electrochemical hydrogen-storage properties of the films were investigated by simulated battery tests. It was found that single-layered LaNi4.25A10.75 film exhibited electrochemical hydrogen-storage properties similar to typical AB5 alloys in bulk, and the maximum discharge capacity of the film was about 220 mAh/g. After 20 charge/discharge cycles, small needle-shaped aluminium oxide was formed on some fractions of the film surface.     

LiCoO2材料的电化学制备及回收研究进展

LiCoO₂电池自商业化以来,在人们的生产和生活中发挥重要作用。电化学法具有简单、高效、环保等特点,被广泛应用于LiCoO₂材料的制备和回收。综述了电化学法制备和回收LiCoO₂材料的研究现状,重点阐述了电化学制备LiCoO₂材料的方法、原理及产物的电化学性能等,以期为电化学方法在制备和回收LiCoO₂材料领域的发展提供基础。     

Orientated Immobilization of FAD-Dependent Glucose Dehydrogenase on Electrode by Carbohydrate-Binding Module Fusion for Efficient Glucose Assay

The discovery or engineering of fungus-derived FAD-dependent glucose 1-dehydrogenase (FAD-GDH) is especially important in the fabrication and performance of glucose biosensors. In this study, a novel FAD-GDH gene, phylogenetically distantly with other FAD-GDHs from Aspergillus species, was identified. Additionally, the wild-type GDH enzyme, and its fusion enzyme (GDH-NL-CBM2) with a carbohydrate binding module family 2 (CBM2) tag attached by a natural linker (NL), were successfully heterogeneously expressed. In addition, while the GDH was randomly immobilized on the electrode by conventional methods, the GDH-NL-CBM2 was orientationally immobilized on the nanocellulose-modified electrode by the CBM2 affinity adsorption tag through a simple one-step approach. A comparison of the performance of the two electrodes demonstrated that both electrodes responded linearly to glucose in the range of 0.12 to 40.7 mM with a coefficient of determination R² > 0.999, but the sensitivity of immobilized GDH-NL-CBM2 (2.1362 × 10⁻² A/(M*cm²)) was about 1-fold higher than that of GDH (1.2067 × 10⁻² A/(M*cm²)). Moreover, a lower detection limit (51 µM), better reproducibility (<5%) and stability, and shorter response time (≈18 s) and activation time were observed for the GDH-NL-CBM2-modified electrode. This facile and easy immobilization approach used in the preparation of a GDH biosensor may open up new avenues in the development of high-performance amperometric biosensors.     

新能源汽车电池负极材料的制备与性能研究

采用原位合成法制备了镍-氧化镍/多孔碳纳米片（Ni-NiO/PCNs）负极材料,对比分析了氯化钠模板、退火温度和退火时间对负极材料物相组成、显微形貌和电化学性能的影响。结果表明,Ni/PCNs、Ni-NiO/C和Ni-NiO/PCNs负极材料都主要含有镍和无定型C相,且后2种负极材料还含有氧化镍相;300 ℃/4 h为Ni-NiO/PCNs负极材料适宜的退火工艺,此时Ni-NiO/PCNs负极材料中Ni-NiO粒子分散性较好且保持着三维片层结构,平均尺寸约为27 nm,Ni-NiO实现了对无定型C的包裹;退火时间过长（6 h）会使得镍粒子过氧化且发生团聚,而温度过高（400 ℃）会使得粒子以团聚为主,三维片层状结构消失。电流密度为1 A/g、循环5 000圈后Ni-NiO/PCNs负极材料的放电比容量为235 mA·h/g,此时的放电比容量约为首圈放电比容量的83.93%;Ni-NiO/C和Ni/PCNs负极材料在充放电循环过程中以及循环5 000圈后的放电比容量和容量保持率都明显低于Ni-NiO/PCNs负极材料,Ni-NiO/PCNs负极材料具有更好的循环稳定性,这主要与其具有独特的多孔三维片层结构有关。     

垃圾焚烧飞灰中氯元素存在形态及深度脱氯的研究

垃圾焚烧飞灰中的氯含量影响其在水泥窑协同处置生料中的占比,因此需要对飞灰做脱氯处理。利用XRD对飞灰氯元素的存在形态研究表明：氯元素以水溶性氯和非水溶性氯2种形态存在于飞灰中,炉排炉飞灰的水溶性氯化物为CaCl₂·Ca（OH）₂·H₂O、CaClOH、CaCl₂·2H₂O、KCl和NaCl,非水溶性氯化物为AlOCl和Ca₁₀（Si₂O₇）₂（SiO₄）Cl₂（OH）₂等;流化床飞灰的水溶性氯以CaCl₂·2H₂O和KCl形式存在,非水溶性氯以AlOCl、Ca₁₀（Si₂O₇）₂（SiO₄）Cl₂（OH）₂和Ca₄OCl₆等形式存在。对水洗脱除水溶性氯的研究结果显示：对于炉排炉飞灰,控制液固比（mL/g,下同）为10+4+2、3次常温水洗,水溶性氯脱除率达97.01%;对于流化床飞灰,控制液固比组合6+6+4、3次常温水洗,水溶性氯脱除率达99.17%;酸、碱洗及高温煅烧均能降低飞灰非水溶性氯含量,其中煅烧处理后的炉排炉飞灰残氯质量分数为0.36%、流化床飞灰为0.45%。