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991.
通过短接电极间隙,开展了3 MV多级多通道缩比开关不同间隙级数和单独触发间隙的自击穿特性分析,结果表明:自击穿电压随电极间隙距离不是线性增加,与Bradley经验公式存在差距。采用Ansoft软件模拟了实验开关不同级数的电场分布,得到不同级数开关电场分布的不均匀系数。结合缩比开关自击穿实验数据、Bradley经验公式和电场分布不均匀系数,在Bradley经验公式中加入开关作用时间因素和电场不均匀系数,得到一个Bradley外推公式,能较好地反应多级多通道气体开关的自击穿电压,使3 MV实际开关自击穿电压理论值与实验值误差减小到5%。 相似文献
992.
993.
Lucas Pailler Pascal Renard Edith Nicol Laurent Deguillaume Angelica Bianco 《Molecules (Basel, Switzerland)》2022,27(22)
FT-ICR MS (Fourier-transform ion cyclotron resonance mass spectrometry) analysis has shown great potential to aid in the understanding of the extremely high molecular diversity of cloud water samples. The main goal of this work was to determine the differences in terms of formula assignment for analytical (i.e., measurement replicates) and experimental replicates of a given cloud water sample. The experimental replicates, obtained by solid phase extraction, were also compared to the results obtained for freeze-dried samples to evaluate whether the presence of salts interferes with the analysis. Two S/N ratios, generally adopted for atmospheric samples, were evaluated, and three different algorithms were used for assignment: DataAnalysis 5.3 (Bruker), Composer (Sierra Analytics), and MFAssignR (Chemical Advanced Resolution Methods Lab). In contrast to other works, we wanted to treat this comparison from the point of view of users, who usually must deal with a simple list of m/z ratios and intensity with limited access to the mass spectrum characteristics. The aim of this study was to establish a methodology for the treatment of atmospheric aqueous samples in light of the comparison of three different software programs, to enhance the possibility of data comparison within samples. 相似文献
995.
本文主要利用解析方法以及二项指数和与Dirichlet特征的性质,研究多项式的特征和与二项三次指数和的混合均值的计算问题,并得到一个较强的渐近公式. 相似文献
996.
Dr. Chi Zhang Dr. Meiling Shao Dr. Dongqing Wu Dr. Zhongyi Li Muzhi Zhao Xiangfei Zhang Prof. Bin Zhai Prof. Yunjun Luo Prof. Xiaoyu Li 《Angewandte Chemie (International ed. in English)》2023,62(52):e202314052
Azide compounds are widely used and especially, polymers bearing pendant azide groups are highly desired in numerous fields. However, harsh reaction conditions are always mandatory to achieve full azidation, causing severe side reactions and degradation of the polymers. Herein, we report the design and preparation of two azide ionic liquids (AILs) with azide anion and triethylene glycol (E3)-containing cation, [P444E3][N3] and [MIME3][N3]. Compared with the traditional sodium azide (NaN3) approach, both AILs showed much higher reaction rates and functional-group tolerance. More importantly, they could act as both reagents and solvents for the quantitative azidation of various polymeric precursors under mild conditions. Theoretical simulations suggested that the outstanding performance of AILs originated from the existence of ion pairs during the reaction, and the E3 moieties played a crucial role. Lastly, after the reaction, the AILs could be easily regenerated, presenting a safer, greener, and highly efficient synthesis route for azide polymers. 相似文献
997.
998.
This article shows that the solution of a backward stochastic differential equation under G-expectation provides a probabilistic interpretation for the viscosity solution of a type of path-dependent Hamilton-Jacobi-Bellman equation. Particularly, a G-martingale can be considered as a nonlinear path-dependent partial differential equation (PDE). We also show that certain class of path-dependent PDEs can be transformed into classical multiple state-dependent PDEs. As an application, the path-dependent uncertain volatility model can be described directly by path-dependent Black-Scholes-Barrenblett equations. 相似文献
999.
1000.