激光陀螺磁灵敏度特性研究

分析、计算了激光陀螺的磁灵敏度特性，并进行了磁灵敏度试验.试验结果及分析表明：在腔体加工准确度不变的情况下，采用合理的设计可以大大降低激光陀螺在某些方向上的磁灵敏度，同时磁试验结果对于设计激光陀螺的磁屏蔽结构具有一定的实用价值.     

激光陀螺锁区特性的研究

从理论和试验两个方面，研究了四边形腔环行激光陀螺的锁区特性.利用环行腔中背向散射光束具有相干性，导出了环行谐振腔综合背向散射与反射镜、反射镜之间的相对位置的关系.在有两个位移反射镜的四边形谐振腔中，理论上得到了综合背向散射系数与谐振腔腔长具有双波长周期.利用综合背向光强实验及锁区与陀螺工作模数实验分别验证了理论的正确性.试验证实散射光的强度与谐振腔的工作模数存在双模周期性，综合背向散射系数大，陀螺锁区大，反之亦然.     

大孔吸附树脂对大豆皂苷的吸附研究

比较了5种大孔吸附树脂对大豆皂苷的吸附等温线、吸附容量、解吸率和吸附动力学。发现ZTC-1树脂对大豆皂苷吸附量大、解吸容易、吸附速度快，是一种良好的大豆皂苷吸附荆，AB-8树脂次之．选择ZTC-l树脂纯化大豆皂苷粗提液，得到大豆皂苷产品纯度为78．2％(干物质)，回收率为93．1％．     

Analysis of total nitrogen and total phosphorus in soil using laser-induced breakdown spectroscopy

Laser-induced breakdown spectroscopy(LIBS) is used to determine the total nitrogen(TN) and total phosphorus(TP) in soil.Quantitative determinations are conducted using the line intensity of the analyte element and element concentration.Calibration models are obtained using ten samples for TN and seven samples for TP.The rest samples are used to validate the results.Strong linear correlations are obtained from the determined TN and TP concentrations.LIBS is a powerful tool for analyzing soil samples to determine nutrient elements by selecting calibration and validation samples with similar matrix composition.     

A Novel Fluorescence Probe for the Reversible Detection of Bisulfite and Hydrogen Peroxide Pair in Vitro and in Vivo

The detection of changes in the reactive oxygen species (ROS)/reactive sulfur species (RSS) couple is important for studying the cellular redox state. Herein, we developed a 1,8-naphthalimide-based fluorescence probe ( NI ) for the reversible detection of bisulfite (HSO₃⁻) and hydrogen peroxide (H₂O₂) in vitro and in vivo. NI has been designed with a reactive ethylene unit which specifically reacts with HSO₃⁻ by a Michael addition reaction mechanism, resulting in the quenching of yellow fluorescence at 580 nm and the appearing of green fluorescence at 510 nm upon excitation at 500 nm and 430 nm, respectively. The addition product ( NI−HSO₃ ) could be specifically oxidized to form the original C=C bond of NI , recovering the fluorescence emission and color. The detection limits of NI for HSO₃⁻ and NI−HSO₃ for H₂O₂ were calculated to be 2.05 μM and 4.23 μM, respectively. The reversible fluorescence response of NI towards HSO₃⁻/H₂O₂ couple can be repeated for at least five times. NI is reliable at a broad pH range (pH 3.0–11.5) and features outstanding selectivity, which enabled its practical applications in biological and food samples. Monitoring the reversible and dynamic inter-conversion between HSO₃⁻ and H₂O₂ in vitro and in vivo has been verified by fluorescence imaging in live HeLa cells, adult zebrafish and nude mice. Moreover, NI has been successfully applied to detect of HSO₃⁻ levels in food samples.     

Utilizing a Photocatalysis Process to Achieve a Cathode with Low Charging Overpotential and High Cycling Durability for a Li-O2 Battery

The practical applications of non-aqueous lithium-oxygen batteries are impeded by large overpotentials and unsatisfactory cycling durability. Reported here is that commonly encountered fatal problems can be efficiently solved by using a carbon- and binder-free electrode of titanium coated with TiO₂ nanotube arrays (TNAs) and gold nanoparticles (AuNPs). Ultraviolet irradiation of the TNAs generates positively charged holes, which efficiently decompose Li₂O₂ and Li₂CO₃ during recharging, thereby reducing the overpotential to one that is near the equilibrium potential for Li₂O₂ formation. The AuNPs promote Li₂O₂ formation, resulting in a large discharge capacity. The electrode exhibits excellent stability with about 100 % coulombic efficiency during continuous cycling of up to 200 cycles, which is due to the carbon- and binder-free composition. This work reveals a new strategy towards the development of highly efficient oxygen electrode materials for lithium-oxygen batteries.     

A tantalum electrode coated with graphene nanowalls for simultaneous voltammetric determination of dopamine,uric acid,L-tyrosine,and hydrochlorothiazide

The authors describe a voltammetric sensor for simultaneous determination of dopamine (DA), uric acid (UA), L-tyrosine (Tyr), and the diuretic drug hydrochlorothiazide (HCTZ). The assay is based on the use of graphene nanowalls deposited on a tantalum substrate. The nanowalls are characterized by scanning electron microscopy, transmission electron microscopy, X-ray diffraction, electrochemical impedance spectroscopy, and cyclic voltammetry. The nanowalls are vertically grown on the substrate by direct-current arc plasma jet chemical vapor deposition. The modified electrode is shown to enable simultaneous differential pulse voltammetric determination of DA, UA, Tyr, and HCTZ. The graphene nanowalls display a large specific surface, high conductivity, and a large number of catalytically active sites for oxidation of analytes. Simultaneous detection is performed best at a pH value of 7.0 and at peak potentials of 0.124 V (vs. SCE) for DA, 0.256 V for UA, 0.536 V for Tyr and 0.708 V for HCTZ. The respective detection limits are 0.04 μM, 0.1 μM, 0.6 μM and 0.4 μM. The results show that this graphene wall modified electrode is a promising tool for the design of sensitive, selective, and stable sensors.

Open image in new window

Graphical abstract The graphene-based differential pulse voltammetric sensor for simultaneous determination of dopamine, uric acid, L-tyrosine, and hydrochlorothiazide exhibits high selectivity, sensitivity, and stability.

     

Microbial fuel cells using natural pyrrhotite as the cathodic heterogeneous Fenton catalyst towards the degradation of biorefractory organics in landfill leachate

An investigation aimed at checking the integration of cathodic pyrrhotite Fenton's reaction with anodic microbial respiration for the enhancement of MFC performance and treatment of a real landfill leachate was carried out. The MFC equipped with a pyrrhotite-coated graphite-cathode generated the maximum power density of 4.2 W/m³ that was 133% higher than graphite-cathode. Concomitantly, electrochemical impedance spectroscopy (EIS) showed that the polarization resistance of pyrrhotite-cathode (92 Ω) was much lower than the graphite-cathode (1057 Ω), indicating that the cathodic overpotential was significantly lowered, probably due to the occurrence of pyrrhotite Fenton's reaction. The in situ generation of Fenton's reagents (Fe²⁺ and H₂O₂) at the pyrrhotite-cathode was demonstrated by the cyclic voltammetry measurement. Besides, reactive oxygen species produced from the pyrrhotite Fenton's reaction were detected and demonstrated to be vital to the enhancement of MFC power output. Further, the effectiveness of this system was examined by treating an old-aged landfill leachate. 77% of color and 78% of COD were removed from the original leachate, indicating that the pyrrhotite not only acted as a cost-effective cathodic catalyst for MFCs in power generation, but also extended the practical merits of traditional MFCs towards advanced oxidation of biorefractory pollutants.     

Host-molecule-coated quantum dots as fluorescent sensors

“Host” molecules, containing a binding site that is highly specific for an analyte “guest,” are used as sensors to register analyte binding through a variety of mechanisms such as colorimetric, fluorescent, or electrochemical signals. There is increasing interest in the host–guest chemistry on the surface of quantum dots (QDs) and in the changes that it produces in the luminescent properties of QDs. The bulk of this study focuses on those QDs with bound host molecules (crown ether, cyclodextrin, calixarene, and porphyrin) and the selectivity they display toward metal ions and small organic molecules.