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41.
In this paper we introduce a new variant of L-curve to estimate the Tikhonov regularization parameter for the regularization of discrete ill-posed problems. This method uses the solution norm versus the regularization parameter. The numerical efficiency of this new method is also discussed by considering some test problems.  相似文献   
42.
基于钢材断裂前必先屈服的基本事实, 以钢材断裂面为屈服面后继扩大直至材料完整性(连续性)发生破坏为假设, 以已有的屈服模型的共同特征为切入点, 建议了各向同性钢材在主应力空间的二次函数型断裂模型和屈服模型. 根据不同钢材的特征应力值, 量化了各向同性钢材的二次函数型断裂模型和屈服模型. 依据不同钢材的特征应力值的相互关系, 建议的各向同性钢材的二次函数型断裂模型和屈服模型相应地描述为主应力空间的圆柱面、椭球面、抛物面和双曲面. 建议的各向同性钢材的二次函数型断裂模型和屈服模型较已有的强度模型更具一般性.  相似文献   
43.
不同类型聚合物溶液对采油残余油的作用机理研究   总被引:6,自引:0,他引:6  
通过实验测定了HPAM溶液和黄原胶溶液的流变性、在多孔介质中的流变性和残余阻力系数 ,计算了衰竭层效应 .用不同的浓度和注入速度进行了驱油实验 .提出聚合物分子缠结作用的增强不仅引起表观粘度增加或衰竭层厚度降低 ,而且使平行于油水界面的拉动残余油的力增加 ,从而使残余油饱和度降低 ,采收率提高 .随浓度增加 ,HPAM溶液的表观粘度和残余阻力系数增加 ,衰竭层厚度减小 ;黄原胶溶液的浓度高于缠结浓度时 ,衰竭层厚度和表观粘度变化不大 .注入速度增加时 ,两种聚合物溶液的衰竭层厚度均降低 ,HPAM溶液的残余阻力系数不变 ,粘弹性增加 ;而黄原胶溶液的残余阻力系数下降 .不同浓度和注入速度情况下两种聚合物溶液的驱油结果证实了文中提出的聚合物分子缠结作用和衰竭层效应对残余油的作用机理 .分子结构的不同是造成两种聚合物溶液在多孔介质中渗流规律和对残余油作用机理的差别的根本原因 .  相似文献   
44.
To apply an irradiation technique to sterilize “Hybrid” biomedical materials including enzymes, we selected papain, a well-characterized plant endopeptidase as a model to examine durability of enzyme activity under the practical irradiation condition in which limited data were available for irradiation inactivation of enzymes. Dry powder and frozen aqueous solution of papain showed significant durability against 60Co-gamma irradiation suggesting that, the commercial irradiation sterilizing method is applicable without modification. Although irradiation of unfrozen aqueous papain solution showed an unusual change of the enzymatic activity with the increasing doses, and was totally inactivated at 15 kGy, we managed to keep the residual activity more than 50% of initial activity after 30-kGy irradiation, taking such optimum conditions as increasing enzyme concentration from 10 to 100 mg/ml and purging with N2 gas to suppress the formation of free radicals.  相似文献   
45.
In NMR spectroscopy, residual dipolar couplings (RDCs) have emerged as one of the most exquisite probes of biological structure and dynamics. The measurement of RDCs relies on the partial alignment of the molecule of interest, for example by using a liquid crystal as a solvent. Here, we establish bacterial type 1 pili as an alternative liquid-crystalline alignment medium for the measurement of RDCs. To achieve alignment at pilus concentrations that allow for efficient NMR sample preparation, we elongated wild-type pili by recombinant overproduction of the main structural pilus subunit. Building on the extraordinary stability of type 1 pili against spontaneous dissociation and unfolding, we show that the medium is compatible with challenging experimental conditions such as high temperature, the presence of detergents, organic solvents or very acidic pH, setting it apart from most established alignment media. Using human ubiquitin, HIV-1 TAR RNA and camphor as spectroscopic probes, we demonstrate the applicability of the medium for the determination of RDCs of proteins, nucleic acids and small molecules. Our results show that type 1 pili represent a very useful alternative to existing alignment media and may readily assist the characterization of molecular structure and dynamics by NMR.  相似文献   
46.
以N,N-二甲基甲酰胺(DMF)为溶剂,丁酮为内标,采用PV-101毛细管色谱柱 (30 m×0.22 mm),氢火焰离子化检测器,建立兰索拉唑中五种有机溶剂甲醇、乙醇、丙酮、二氯甲烷、乙酸乙酯残留量的定量分析方法。五种有机溶剂检出限分别为0.002 4%,0.002 4%, 0.001 2%,0.000 6%,0.000 6%;在10-1000 mg·L-1浓度范围内,各组分线性关系良好;对应的平均回收率分别为100.8%±3.6%,102.1%±2.3%,99.97%±4.1%,99.63%±2.7%, 102.3%±3.5%。  相似文献   
47.
GC-MS法测定拟除虫菊酯类农药残留   总被引:3,自引:0,他引:3  
介绍了蔬菜水果中8种拟除虫菊酯农药残留的快速检测方法。采用选择离子-气相色谱-质谱联用(SIM-GC-MS)方式,依据保留时间和特征离子丰度比对农药进行确证。此方法可以在13.50 min内快速检测拟除虫菊酯农药残留,并可同时定性和定量,用于蔬菜水果等多种作物的检验。回收率在75%~108%间,相对标准偏差<10%,检出限为0.000 90~0.008 4 mg.kg-1。  相似文献   
48.
The direct electron transfer reaction of glucose oxidase (GOx) at a bare silver electrode is verified. The electron transfer number n = 2, electron transfer coefficient α = 0.45 and rate constant of the electrochemical reaction Ks = 0.1 s−1 are obtained. This communication presents a multimolecular adsorption model to explain the properties of the direct electron reaction between GOx and bare silver electrodes. The residual valence force may be an important factor to ensure a direct electron transfer reaction on the bare electrode. On the basis of the experimental fact that only biologically active GOx exhibits electrochemical activity in solution, a facile analytical method for analyzing the active GOx concentration is developed. The results determined correspond very well to that of a spectrometric method.  相似文献   
49.
提出了一种以固相微萃取与气相色谱-氢火焰联用技术为基础的测定食品包装材料中15种常用有机溶剂(苯类、醇类、酮类、酯类等)的方法。选择聚二甲亚砜作为固相微萃取的萃取相,采用DB-624毛细管色谱柱进行分离。在优化的试验条件下,15种有机残留溶剂在20min内能很好地分离,15种溶剂的测定下限(10S/N)为0.08~0.69μg.dm-2。加标回收率为60.0%~115.0%,相对标准偏差(n=5)为2.17%~8.34%。  相似文献   
50.
Electrochemical impedance spectroscopy allows the examination of corrosion susceptibility and resistance for different construction materials, in particular the determination of the properties of their passive films. This technique makes possible the analysis of electrochemical processes in time domain, including rapid phenomena such as changes in the properties of passive films, but it has never been used for passive layer cracking examination. In many cases, fracture of the passive film under tensile stresses leads to stress corrosion cracking. Therefore, investigations of passive layer cracking on austenitic stainless steels under tensile stresses facilitate the understanding of the mechanism of stress corrosion cracking in these common engineering materials. The effect of static tensile stresses on the passive film cracking behaviour of type 304L stainless steel immersed in 0.5 M NaCl solution at room temperature has been investigated. This paper presents the impedance spectra obtained for 304L stainless steel samples at different potential values.Contribution to the 3rd Baltic Conference on Electrochemistry, Gdansk-Sobieszewo, Poland, 23–26 April 2003Dedicated to the memory of Harry B. Mark, Jr. (28 February 1934–3 March 2003)  相似文献   
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