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含磷、硫、氮配原子的钴羰基簇合衍生物的合成和表征 总被引:1,自引:0,他引:1
过渡金属原子簇化学是当今化学学科中非常活跃的研究领域之一 ,这类簇合物大多有着新颖的几何构型和多样化的成键方式 ,并且具有独特的催化性能[1 ] 。迄今为止 ,人们合成了多种含磷、硫、氮等原子的铁、钴、钌等羰基簇合衍生物 ,但其中三种以上原子同时配位的情况并不多见 ,有金振兴等的含C、S、N配原子的三核钴簇[2 ] ;Luga和Cabeza的三钌簇[3 ,4] 以及Chihara等合成的五核钌簇[5] ,其分子中都有P、N、O三原子配位。我们利用复杂的含P、S、N等可配原子的有机配前体与二元钴羰合物反应 ,合成了一系列三核、四核… 相似文献
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对利用微波放电直接解离Cl2生成Cl, Cl与HN3反应生成NCl(a1Δ )和NCl(b1∑)的过程进行了实验研究。得到了较强的NCl(a1Δ 和NCl(b1∑)自发辐射光谱,考察了Cl2流量和He/Cl2配比对NCl(a1Δ 和NCl(b1∑)生成的影响。发现对于一定的He流量,Cl2流量对NCl(a1Δ 和NCl(b1∑)生成的影响存在一最佳范围,而最佳He/Cl2配比不是一定值,而是随He流量升高而变大,在实验所考察的He流量范围(5~40 L/min)内,最佳He/Cl
2配比在30∶1~100∶1之间。 相似文献
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利用几何特性及神经网络进行人脸探测技术的研究 总被引:4,自引:0,他引:4
在人脸识别过程中 ,首先也是最重要的一个环节是人脸探测 ,因为一旦从图像中定位并提取到了人脸 ,那么下一步的人脸识别工作就变得非常容易。眼睛是人脸图像中最容易探测的部位 ,而且通过探测双眼来发现人脸最符合人的视觉习惯。提出了一种基于几何特征分析和人工神经网络的由粗到细的两级人脸探测方法。在第一级中 ,眼睛和脸是通过测量眼睛的尺寸和眼睛与脸的位置关系探测到的 ,第一级的输出是一个尺寸归一化的人脸 ,但偶尔也伴随着一个或多个因对复杂背景中与眼睛类似的物体的误判而得到的非人脸图像 ;第二级神经网络正是用来过滤掉第一级中被误判的人脸。实验表明 ,这种由粗到细的两级人脸探测系统具有很高的稳定性和探测正确率 相似文献
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随着信息产业国际化趋势的发展,广域网理论的研究显得越来越重要,中提出了网络的分形生长结构模型和生长方法,从全新的角度讨论广域网的生长、发展的过程。该结构模型将是描述互连广域的重要工具。 相似文献
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报道了用光子能量低于GaAs禁带宽度的红外激光脉冲,触发电极间隙为3mm和8mm的半绝缘GaAs光电导开关的实验结果。使用单脉冲能量为1.9mJ的1 064nm Nd:YAG激光触发开关, 在偏置电压分别为3kV和5kV条件下,光电导开关分别工作于线性和非线性模式。用900nm半导体激光器和1 530nm掺铒光纤激光器分别进行触发实验,得到了重复频率分别为5kHz和20MHz的电脉冲波形。结果表明,半绝缘GaAs光电导开关可以吸收大于本征吸收限波长红外激光脉冲。 相似文献
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Structure Modification Function of g‐C3N4 for Al2O3 in the In Situ Hydrothermal Process for Enhanced Photocatalytic Activity
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Prof. Fa‐tang Li Shao‐jia Liu Ya‐bin Xue Dr. Xiao‐jing Wang Dr. Ying‐juan Hao Dr. Jun Zhao Rui‐hong Liu Prof. Dishun Zhao 《Chemistry (Weinheim an der Bergstrasse, Germany)》2015,21(28):10149-10159
Heterojunctions of g‐C3N4/Al2O3 (g‐C3N4=graphitic carbon nitride) are constructed by an in situ one‐pot hydrothermal route based on the development of photoactive γ‐Al2O3 semiconductor with a mesoporous structure and a high surface area (188 m2g?1) acting as electron acceptor. A structure modification function of g‐C3N4 for Al2O3 in the hydrothermal process is found, which can be attributed to the coordination between unoccupied orbitals of the Al ions and lone‐pair electrons of the N atoms. The as‐synthesized heterojunctions exhibit much higher photocatalytic activity than pure g‐C3N4. The hydrogen generation rate and the reaction rate constant for the degradation of methyl orange over 50 % g‐C3N4/Al2O3 under visible‐light irradiation (λ>420 nm) are 2.5 and 7.3 times, respectively, higher than those over pristine g‐C3N4. The enhanced activity of the heterojunctions is attributed to their large specific surface areas, their close contact, and the high interfacial areas between the components as well as their excellent adsorption performance, and efficient charge transfer ability. 相似文献
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Effect of formulation of silica‐based solution on corrosion resistance of silicate coating on hot‐dip galvanized steel
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Shuang‐hong Zhang Gang Kong Zi‐wen Sun Chun‐shan Che Jin‐tang Lu 《Surface and interface analysis : SIA》2016,48(3):132-138
Several silica‐based solutions with 50 g/l of SiO2 were prepared from sodium silicate solutions and silica sol; the silicate conversion coatings were obtained by immersing hot‐dip galvanized steel sheets in these solutions. These solutions were characterized using high‐resolution transmission electron microscopy and 29Si nuclear magnetic resonance; the morphology of the coatings was observed by SEM and atomic force microscopy while the corrosion resistance was evaluated by electrochemical measurements as well as neutral salt spray tests. The results show that the coatings obtained from the single silica sol solution had poor adhesion and the coating obtained from the sodium silicate solution with low SiO2/Na2O molar ratio was uneven. By adding the silica sol to the silicate solution with low molar ratio, uniform coatings with better protection property were obtained. According to the results of 29Si nuclear magnetic resonance spectra, the effects of the distribution of silicate anions with various polymerization degrees in the silica‐based solutions on the microstructure and corrosion resistance of the silicate coatings are discussed. Copyright © 2016 John Wiley & Sons, Ltd. 相似文献