No abstract

The effect of the DS ratio is evaluated and a correction approach is proposed to improve the accuracy and robustness of the proposed DS Cd isotope analysis.

CdS nanowire/ZnO nanosphere materials (CdS/ZnO) with hierarchical structure were synthesized by a three-step solvothermal process. XRD, FESEM and TEM analysis confirmed the growth of ZnO nanospheres on the surface of CdS nanowires (NWs). The transient photovoltage (TPV) measurements revealed that the interface between CdS and ZnO can inhibit the recombination of photogenerated excess carriers and prolong the lifetime of excess carriers in CdS/ZnO materials. Moreover, the CdS/ZnO materials exhibit a dramatic improvement in optoelectronic performance and visible-light-irradiation gas sensing activity, which gave 1 order of magnitude larger than that of CdS NWs in response to formaldehyde. The enhancement of sensing properties is attributed to the interfacial transport of excess carriers.

In this paper, a sensitive atomic emission spectrometer (AES) based on a new low power and low argon consumption (<8 W, 100 mL min) miniature direct current (dc) atmospheric pressure glow discharge (APGD) plasma (3 mm × 5 mm) excitation source was developed for the determination of arsenic in water samples. In this method, arsenic in water was reduced to AsH by hydride generation (HG), which was then transported to the APGD source for excitation and detected by a compact CCD (charge-coupled device) microspectrometer. Different parameters affecting the APGD and the hydride generation reactions were investigated. The detection limit for arsenic with the proposed APGD-AES was 0.25 μg L, and the calibration curves were found to be linear up to 3 orders of magnitude. The proposed method was successfully applied to the determination of certified reference material (GBW08605), tap water, pond water, groundwater, and hot spring samples. Measurements from the APGD analyzer showed good agreement with the certified value/values obtained with well-established hydride generation atomic fluorescence spectrometry (HG-AFS). These results suggest that the developed robust, cost-effective, and fast analyzer can be used for field based arsenic determination and may provide an important tool for arsenic contamination and remediation programs.

In the present study, a novel and sensitive liquid spray dielectric barrier discharge induced plasma-chemical vapor generation technique (LSDBD-CVG) is developed for the determination of lead concentration by inductively coupled plasma mass spectrometry (ICPMS). The dissolved Pb is readily converted to volatile species by LSDBD plasma induced chemical processes in the presence of 5% (v/v) formic acid in a supporting electrolyte (HCl, 0.01 mol L). In this LSDBD approach, the sample solution is converted to aerosol and simultaneously mixed with the DBD plasma generated at the nozzle of a pneumatic nebulizer, which greatly facilitates Pb vapor generation because of the enhanced interaction of sprayed analytes and the plasma. Optimal conditions for LSDBD-CVG were identified, and the interference effects from other metal ions were assessed. Under optimized conditions, the detection limit of Pb was found to be 0.003 μg L. The repeatability, expressed as the relative standard deviation (RSD) of the peak height, for the five replicate measurements of 0.03 and 1 μg L lead standard, were 2.1% and 1.7%, respectively. Compared with other vapor generation methods, this new LSDBD-CVG offers several advantages including no requirement of unstable reagents, fast response, and easy coupling with flow injection, along with high tolerance for coexisting ions. The accuracy of the proposed method is demonstrated by successful analysis of Pb in reference material of stream sediment (GBW07311), soil (GBW07403), basalt (BCR-2), and simulated water sample (GBW08601). The proposed LSDBD-CVG extends the scope of elements accessible by plasma-CVG and provides an alternative efficient green approach for the vapor generation of Pb.