排序方式: 共有116条查询结果,搜索用时 15 毫秒
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借助于Mott-Schottky方程分析了成膜电位、成膜时间、成膜温度以及氯离子等因素对22Cr双相不锈钢在碳酸氢钠/碳酸钠缓冲溶液中所成钝化膜半导体性能的影响, 同时借助于X射线光电子能谱(XPS)技术分析了所成钝化膜的组成. 结果表明: 22Cr双相不锈钢在碳酸氢钠/碳酸钠缓冲溶液中所成钝化膜呈n-p型半导体结构, 钝化膜内施主/受主密度随成膜电位增加、成膜时间延长、成膜温度降低、以及介质中氯离子浓度的降低而减小, 同时膜对基体保护作用随这些因素变化而增强. 钝化膜的XPS分析表明, 钝化膜呈现双层结构, 外层膜主要由三价铁的氧化物(Fe2O3)组成, 内层膜主要由三价铬氧化物(Cr2O3)以及少量二价铁氧化物(FeO)组成. 相似文献
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通过数值模拟方法, 研究了在具有稳定次阈值振荡特性的二维映射神经元体系中, 噪声对体系非线性动力学的调控作用. 通过计算发现了噪声诱导的动作电位和随机共振现象. 另外,还研究了体系的控制参数及输入信号的频率对体系动力学的影响, 发现了该体系中频率依赖的随机共振现象.
关键词:
二维映射神经元模型
次阈值振荡
高斯白噪声
随机共振 相似文献
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Li WY Xiong XQ Zhao DM Shi YF Yang ZH Yu C Fan PW Cheng MS Shen JK 《Molecules (Basel, Switzerland)》2012,17(5):5497-5507
A series of novel quinoline-3-carboxamide derivatives 10-17 and 23-27 were designed and synthesized as cholesteryl ester transfer protein (CETP) inhibitors. All of them exhibited activity against CETP. Particularly, compounds 24 and 26 displayed the best activity against CETP with the same inhibitory rate of 80.1%. 相似文献
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纤维素重复单元的羟基上引入足够数量的柔性分子链,有可能在破坏纤维素分子链间氢键的同时起到内增塑作用,从而赋予纤维素熔融流动性.由纤维素酯化反应得到的一些短链取代的纤维素酯[如纤维素醋酸酯(CA)、纤维素丙酸酯(CP)等]具有热塑性,但需要在外加大量增塑剂条件下才能熔融加工[1].接枝共聚合是改变纤维素物理化学性质的另一种有效方法[2~4]。 相似文献
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N80油套管钢钝化膜的光电化学性能 总被引:1,自引:0,他引:1
采用电容测试法研究了N80油套管钢在浓度为0.5 mol/L NaHCO3溶液中形成钝化膜的半导体性能,结合Mott-Schottky方程分析了测试频率,成膜电位和C l-浓度对钝化膜半导体性能的影响。电容测试结果表明,钝化膜呈n型半导体特性,Mott-Schottky曲线的斜率随着测试频率的增加、成膜电位的正移和溶液中氯离子浓度的增加而增加,相应地膜内的施主密度减小。光电化学实验结果表明,光电流强度随成膜电位的正移及成膜时间的延长而增加,这主要归功于高电位和长时间下所成的钝化膜具有比较均匀的组成,光激发所成的空位或电子在膜内的迁移率的增加。 相似文献
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Best Spatiotemporal Performance Sustained by Optimal Number of Random Shortcuts on Complex Networks 下载免费PDF全文
The spatial synchronization and temporal coherence of FitzHugh-Nagumo (FHN) neurons on complex networks are numerically investigated. When an optimal number of random shortcuts are added to a regular neural chain, the system can reach a state which is nearly periodic in time and almost synchronized in space. More shortcuts do not increase the spatial synchronization too much, but will obviously destroy the temporal regularity. 相似文献
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Thirteen novel triterpenoid saponins, designed as amide derivatives of the natural cytotoxic saponin β-hederin, were synthesized by a stepwise glycosylation strategy. The in vitro cytotoxic activity of these compounds was evaluated against five different tumor cell lines. Most of the evaluated compounds showed effective inhibitory activity against at least one tumor cell line at micromolar concentrations. The preliminary structure-activity relationships (SAR) indicate that mide derivatization at C-28 resulted in highly cytotoxic derivatives on specific tumor cell lines, and also resulted in an increase in the antitumor selectivity of β-hederin. 相似文献
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