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31.
32.
It is considered the class of Riemann surfaces with dimT1 = 0, where T1 is a subclass of exact harmonic forms which is one of the factors in the orthogonal decomposition of the spaceΩH of harmonic forms of the surface, namely The surfaces in the class OHD and the class of planar surfaces satisfy dimT1 = 0. A.Pfluger posed the question whether there might exist other surfaces outside those two classes. Here it is shown that in the case of finite genus g, we should look for a surface S with dimT1 = 0 among the surfaces of the form Sg\K , where Sg is a closed surface of genus g and K a compact set of positive harmonic measure with perfect components and very irregular boundary. 相似文献
33.
Improved performance of near UV light-emitting diodes with a composition-graded p-AlGaN irregular sawtooth electron-blocking layer 下载免费PDF全文
We investigate the performances of the near-ultraviolet(about 350 nm-360 nm) light-emitting diodes(LEDs) each with specifically designed irregular sawtooth electron blocking layer(EBL) by using the APSYS simulation program.The internal quantum efficiencies(IQEs),light output powers,carrier concentrations in the quantum wells,energy-band diagrams,and electrostatic fields are analyzed carefully.The results indicate that the LEDs with composition-graded pAl_xGa_(1-x)N irregular sawtooth EBLs have better performances than their counterparts with stationary component p-AlGaN EBLs.The improvements can be attributed to the improved polarization field in EBL and active region as well as the alleviation of band bending in the EBL/p-AlGaN interface,which results in less electron leakage and better hole injection efficiency,thus reducing efficiency droop and enhancing the radiative recombination rate. 相似文献
34.
A weighting of the edges of a hypergraph is called vertex‐coloring if the weighted degrees of the vertices yield a proper coloring of the graph, i.e. every edge contains at least two vertices with different weighted degrees. In this article, we show that such a weighting is possible from the weight set for all hypergraphs with maximum edge size and not containing edges solely consisting of identical vertices. The number is best possible for this statement. 相似文献
35.
Chaonan Xie Qin Li Gang Han Huan Liu Jien Yang Jincheng Li 《Biomedical chromatography : BMC》2019,33(5)
Tricaine methanesulfonate is one of most commonly used anesthetics in fish during blood sampling, artificial propagation and long‐distance transportation. In this study, an accurate method for the quantitative determination of tricaine in fish samples by a stable isotope dilution assay coupled with high‐performance liquid chromatography–triple quadrupole mass spectrometry was developed. Tricaine‐D5 was synthesized and used as an isotopically labeled internal standard for the determination of tricaine. The analytical performance of the method was validated for tricaine determination in marine fish and freshwater fish. The determination of tricaine was linear in the range of 2.0–200.0 μg L?1. The limit of detection and limit of quantitation for fish muscle tissues were 1.0 and 4.0 μg kg?1, respectively. Good recoveries were obtained in the range of 92.08–97.50%. The inter‐ and intra‐assay relative standard deviations (RSD values) were investigated, and the values were 0.39–3.01 and 0.85–2.77%, respectively. The values of CCα and CCβ were 10.21–10.43 and 10.42–10.87 μg kg?1, respectively. The clearance of MS‐222 from grass carp was further studied using our method. The results demonstrate that MS‐222 could be well absorbed and rapidly eliminated after bath administration. 相似文献
36.
《Electroanalysis》2017,29(3):880-889
A new method for modifying electrodes with Ag nanoparticles (AgNPs) using electrospray deposition for sensitive, selective detection of Zn(II), Cd(II), and Pb(II) in aerosol samples when combined with Bismuth and Nafion coating and square‐wave anodic stripping voltammetry (SWASV) is reported. Carbon stencil‐printed electrodes (CSPEs) fabricated on a polyethylene transparency (PET) sheet were produced for an inexpensive, simple to fabricate, disposable sensor that can be used with the microliter sample volumes for analysis. Sensor performance was improved by modifying the electrode surface with electrospray‐deposited AgNPs. The use of electrospray deposition resulted in more uniform particle dispersion across the electrode surface when compared to drop‐casting. Using AgNP‐modified electrodes combined with Bi and Nafion, experimental detection limits (LODs) of 5.0, 0.5, and 0.1 μg L−1 for Zn(II), Cd(II), and Pb(II), respectively, were achieved. The linear working ranges were 5.0–400.0 μg L−1, 0.5–400.0 μg L−1, and 0.1–500.0 μg L−1 for Zn(II), Cd(II), and Pb(II), respectively. Interference studies showed Cu(II) was the only metal that interfered with this assay but inference could be eliminated with the addition of ferricyanide directly to the sample solution. This electrochemical sensor was applied for the simultaneous determination of Zn(II), Cd(II), and Pb(II) within source particulate matter (PM) samples collected on filters using an aerosol test chamber. 相似文献
37.
《Electrophoresis》2017,38(3-4):460-468
Ultrasound‐assisted extraction (UAE), cloud point extraction (CPE), and ultrasound back‐extraction (UABE) techniques have been coupled for lixiviation, preconcentration, and cleanup of polybrominated diphenyl ethers (PBDEs) from milk samples for determination by gas chromatography‐electron capture detection (GC‐ECD). Physicochemical parameters that affect the efficiency of the extraction system were investigated using a design of experiments based on multivariate statistical tools, and considering the sample matrix along the development. The coupling of the leaching step, UAE, enhanced ca. 3.5 times the extraction efficiency of the former sample preparation methodology (CPE‐UABE) leading to cleaner sample extracts suitable for GC analysis. Under optimum conditions, the proposed methodology exhibits successful performance in terms of linearity and precision, with recoveries in the range of 68–70% and LODs within the range 0.05–0.5 ng/g dry weight (d.w.). The proposed sample preparation methodology coupled three green analytical techniques. It expands the application frontiers of CPE for the analysis of biological samples by GC. The optimized methodology was used for determination of PBDEs in powder milk samples, from both commercial and human sources. 相似文献
38.
Ricardo E. Rivas Ignacio López-GarcíaManuel Hernández-Córdoba 《Spectrochimica Acta Part B: Atomic Spectroscopy》2009
A new procedure for the determination of inorganic arsenic (III,V) and antimony (III,V) in water samples by dispersive liquid–liquid micro extraction separation and electrothermal atomic absorption spectrometry (ETAAS) is presented. At pH 1, As(III) and Sb(III) are complexed with ammonium pyrrolidine dithiocarbamate and extracted into the fine droplets formed when mixing carbon tetrachloride (extraction solvent), methanol (disperser solvent) and the sample solution. After extraction, the phases are separated by centrifugation, and As(III) and Sb(III) are determined in the organic phase. As(V) and Sb(V) remain in the aqueous layer. Total inorganic As and Sb are determined after the reduction of the pentavalent forms with sodium thiosulphate. As(V) and Sb(V) are calculated by difference. The detection limits are 0.01 and 0.05 µg L− 1 for As(III) and Sb(III), respectively, with an enrichment factor of 115. The relative standard deviation is in the 2.9–4.5% range. The procedure has been applied to the speciation of inorganic As and Sb in bottled, tap and sea water samples with satisfactory results. 相似文献
39.
Walter N.L. dos Santos Geovani C. Brandão Lindomar A. Portugal Jorge M. David Sérgio L.C. Ferreira 《Spectrochimica Acta Part B: Atomic Spectroscopy》2009
This paper proposes the use of photo-oxidation with UV radiation/H2O2 as sample pretreatment for the determination of iron and manganese in wines by flame atomic absorption spectrometry (FAAS). The optimization involved the study of the following variables: pH and concentration of buffer solution, concentrated hydrogen peroxide volume and irradiation time. The evaluation of sample degradation was monitored by measuring the absorbance at the maximum wavelength of red wine (530 nm). Using the experimental conditions established during the optimization (irradiation time of 30 min, oxidant volume of 2.5 mL, pH 10, and a buffer concentration of 0.15 mol L− 1), this procedure allows the determination of iron and manganese with limits of detection of 30 and 22 μg L− 1, respectively, for a 5 mL volume of digested sample. The precision levels, expressed as relative standard deviation (RSD), were 2.8% and 0.65% for iron and 2.7% and 0.54% for manganese for concentrations of 0.5 and 2.0 mg L− 1, respectively. Addition/recovery tests for evaluation of the accuracy were in the ranges of 90%–111% and 95%–107% for iron and manganese, respectively. This digestion procedure has been applied for the determination of iron and manganese in six wine samples. The concentrations varied from 1.58 to 2.77 mg L− 1 for iron and from 1.30 to 1.91 mg L− 1 for manganese. The results were compared with those obtained by an acid digestion procedure and determination of the elements by FAAS. There was no significant difference between the results obtained by the two methods based on a paired t-test (at 95% confidence level). 相似文献
40.
Gel filtration chromatography using a TSKgel G2000 SW column coupled with differential refractive index detection was used to analyse five grades of polyvinyl alcohol. Limits of detection and quantification for the assay were 0.14 mg mL–1, 0.47 mg mL–1 respectively. The inter and intra-day co-efficient of variance were both <7%. There was a significant difference (p<0.05, n=5) between the calibration curves across the five grades of PVA due to a refractive index range of 13.0790 –1.3181 (n=3). The assay accuracy was 98.99% ± 8.97% (n=5) and 90.60% ± 7.87% (n=5) of a spiked PVA sample was recovered from a commercial formulation. 相似文献