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从实验和理论两方面研究了不同布置方式对加热U型管不稳定性的影响。实验在氟利昂-113试验台上进行,研究了不同布置U型管在三种压力工况,六种加热工况及各种流量下的流动不稳定性。理论研究得出了系统稳定性的判据,比较了不同布置方式U型管的脉动起始边界;并对实际工业现场的U型管布置方式进行了模拟数值计算,比较了在较高系统压力下不同布置方式U型管的脉动起始边界  相似文献   
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粘塑性薄壁管中复合应力波的传播特性研究   总被引:3,自引:0,他引:3  
以本构关系一般理论为基础,导出了计及材料功硬化效应和应变率硬化效应的粘塑性薄壁管的本构关系及管中复合应力波的控制方程,应用有限差分方法研究了在压扭复合冲击载荷作用下粘塑性薄壁管中复合应力波的传播特性与演化规律,分析了复合应力波的耦合效应以及薄壁管中粘塑性参数和功硬化效应对复合应力波传播与演化规律的影响,并对有关现象进行了分析和解释。  相似文献   
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We have demonstrated that the fragments of Telaprevir can act as organocatalysts for asymmetric aldol reactions between aromatic aldehydes and acetone under mild conditions. The reaction conditions have been optimized in terms of the catalyst nature, choice of temperature, solvent, additive, and the catalyst loading. Under proper conditions, fairly good yield and enantioselectivity have been achieved.  相似文献   
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Danshen (DS) is a widely used traditional Chinese medicine for treating cardiovascular and cerebrovascular diseases. A simple, rapid and sensitive method was developed for identification of the in vivo metabolites in urine of WZS‐miniature pigs after oral administration of DS decoction by HPLC coupled with diode array detection with electrospray ionization tandem ion trap and time‐of‐flight mass spectrometry. This method has been successfully applied to simultaneous identification of 50 compounds (including 11 new ones) in pig urine. In addition, one new compound, (3‐hydroxyphenyl) crylic acid glycine methyl ester (C1), along with eight known ones were first isolated by column chromatography and identified by spectroscopic means, including 1D/2DNMR and mass spectrometry, as reference substances. Ten phenolic compounds (protocatechuic aldehyde, protocatechuic acid, caffeic acid, danshensu, ferulic acid, isoferulic acid, rosmarinic acid and salvianolic acid A/B/D) were found to be the main absorbed original constituents of DS decoction, which underwent the metabolic reactions of glucuronidation, sulfation, methylation, hydrogenation and glycine conjugation in vivo. In conclusion, the developed method is applicable to the analysis and identification of constituents in biological matrices after administration of DS decoction. Copyright © 2012 John Wiley & Sons, Ltd.  相似文献   
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Four new prenylindole derivatives, (R)‐6‐(2,3‐dihydroxy‐3‐methylbutyl)indole (1), (R)‐6‐(2,3‐dihydroxy‐3‐methylbutyl)indolin‐2‐one (2), and an unseparated mixture of (Z)‐6‐(4‐hydroxy‐3‐methylbut‐2‐en‐1‐yl)indolin‐2‐one (3a) and (E)‐6‐(4‐hydroxy‐3‐methylbut‐2‐en‐1‐yl)indolin‐2‐one (3b) with a ratio of 3 : 2, were isolated from the culture broth of a streptomycete isolated from Ailuropoda melanoleuca feces. Their structures were elucidated on the basis of 1D and 2D NMR spectroscopic techniques. The absolute configuration of 1 was determined by Mosher's method. Copyright © 2013 John Wiley & Sons, Ltd.  相似文献   
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In this paper, we consider the zero-norm minimization problem with linear equation and nonnegativity constraints. By introducing the concept of generalized Z-matrix for a rectangular matrix, we show that this zero-norm minimization with such a kind of measurement matrices and nonnegative observations can be exactly solved via the corresponding p-norm minimization with p in the open interval from zero to one. Moreover, the lower bound of sample number for exact recovery is allowed to be the same as the sparsity of the original image or signal by the underlying zero-norm minimization. A practical application in communications is presented, which satisfies the generalized Z-matrix recovery condition.  相似文献   
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Neopanaxadiol (NPD), a major ginsenoside in Panax ginseng C. A. Meyer (Araliaceae), was reported to have neuroprotective effect. In this study, a method of ultra‐performance liquid chromatography quadrupole time‐of‐flight mass spectrometry (UPLC/QTOF‐MS) was developed and validated for quantitative analysis of NPD in tissues, urine and feces, using liquid–liquid extraction (LLE) to isolate NPD from different biological samples, and chromatographic separation was performed on an Agilent Zorbax Stable Bond C18 (2.1 × 50 mm, 1.8 µm) column with 0.1% formic acid in water and acetonitrile. All standard calibration curves were linear (all r2 > 0.995) within the test range. After oral administration, NPD was extensively distributed to most of the tissues without long‐term accumulation. The higher levels were observed in stomach and intestine, followed by kidney and liver. Approximately 64.56 ± 20.32% of administered dose in feces and 0.0233 ± 0.0356% in urine were found within 96 h, which indicated that the major elimination route was fecal excretion. This analytical method was applied to the study of NPD distribution and excretion in rats after oral intake for the first time. The results we found here are helpful for us to understand the pharmacological effects of NPD, as well as its toxicity. Copyright © 2014 John Wiley & Sons, Ltd.  相似文献   
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