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In this article, compact representation of spatial variation of Head-Related Transfer Function (HRTF) or its corresponding inverse Fourier transform, namely Head-Related Impulse Response (HRIR) based on Principal Components Analysis (PCA), which is called the Spatial Principal Component Analysis (SPCA), is investigated, focusing on effect of domain selection. The SPCA was carried out for a database of HRTFs in all directions by selecting the domain as one of the HRIRs, the complex HRTFs, the frequency amplitudes of HRTFs, and log-amplitudes of HRTFs. In the latter two cases the minimum phase approximation was incorporated. Comparison of the accuracy in both time and frequency domains showed that the most compact representation is obtained by using the frequency amplitudes of HRTFs when the minimum phase approximation is acceptable, and the complex HRTFs bring about the most compact representation when the minimum phase approximation is not acceptable. 相似文献
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In the present work we investigate the behavior of all three components of persistent spin current in a quasi-periodic Fibonacci ring subjected to Rashba and Dresselhaus spin–orbit interactions. Analogous to persistent charge current in a conducting ring where electrons gain a Berry phase in presence of magnetic flux, spin Berry phase is associated during the motion of electrons in presence of a spin–orbit field which is responsible for the generation of spin current. The interplay between two spin–orbit fields along with quasi-periodic Fibonacci sequence on persistent spin current is described elaborately, and from our analysis, we can estimate the strength of any one of two spin–orbit couplings together with on-site energy, provided the other is known. 相似文献
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F. Farid 《Linear and Multilinear Algebra》2013,61(3):223-239
An upper bound for the number of components of the numerical range of matrix polynomials is established. We also establish a necessary condition and a sufficient condition for the connectedness of the numerical range of a quadratic selfadjoint matrix polynomial. The boundary of the numerical range of linear matrix polynomials is also considered. 相似文献
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X射线荧光光谱分析法对高风险零部件快速的RoHS检测,使用这种"快速筛选"的方法有以下两点目的:一方面审核供应商提交的有毒有害物质符合性声明的准确性,另一方面也节约企业检测成本。 相似文献
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Shurong Wang Xiujuan Guo Kaige Wang Zhongyang Luo 《Journal of Analytical and Applied Pyrolysis》2011,91(1):183-189
There has been much interest in the utilization of biomass-derived fuels as substitutes for fossil fuels in meeting renewable energy requirements to reduce CO2 emissions. In this study, the pyrolysis characteristics of biomass have been investigated using both a thermogravimetric analyzer coupled with a Fourier-transform infrared spectrometer (TG-FTIR) and an experimental pyrolyzer. Experiments have been conducted with the three major components of biomass, i.e. hemicellulose, cellulose, and lignin, and with four mixed biomass samples comprising different proportions of these. Product distributions in terms of char, bio-oil, and permanent gas are given, and the compositions of the bio-oil and gaseous products have been analysed by gas chromatography-mass spectrometry (GC-MS) and gas chromatography (GC). The TG results show that the thermal decomposition of levoglucosan is extended over a wider temperature range according to the interaction of hemicellulose or lignin upon the pyrolysis of cellulose; the formation of 2-furfural and acetic acid is enhanced by the presence of cellulose and lignin in the range 350-500 °C; and the amount of phenol, 2,6-dimethoxy is enhanced by the integrated influence of cellulose and hemicellulose. The components do not act independently during pyrolysis; the experimental results have shown that the interaction of cellulose and hemicellulose strongly promotes the formation of 2, 5-diethoxytetrahydrofuran and inhibits the formation of altrose and levoglucosan, while the presence of cellulose enhances the formation of hemicellulose-derived acetic acid and 2-furfural. Pyrolysis characteristics of biomass cannot be predicted through its composition in the main components. 相似文献
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An isocratic liquid chromatographic method for determination of acetaminophen (AMP), caffeine (CAF), chlorphenamine maleate (CPM) and guaiacol glyceryl ether (GGE) in a compound cold formulation is described. Separation and quantitation were achieved on a Diamonsil C18 column using a binary mixture of methanol and 1.5% aqueous acetic acid (55: 45, v/v, pH 3.6) as mobile phase delivered at 0.4 mL min–1. Single wavelength detection was at 220 nm for all four drugs and the run time was < 10 min. The linearity, accuracy and precision of the method were found to be acceptable over the concentration ranges: 16.0–127.8 g mL–1 for AMP, 6.0–48.2 g mL–1 for CAF, 5.0–40.0 g mL–1 for CPM and 10.1–80.6 g mL–1 for GGE. 相似文献
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