首页 | 本学科首页   官方微博 | 高级检索  
文章检索
  按 检索   检索词:      
出版年份:   被引次数:   他引次数: 提示:输入*表示无穷大
  收费全文   1篇
  免费   0篇
  国内免费   2篇
化学   2篇
物理学   1篇
  2022年   1篇
  2016年   1篇
  2008年   1篇
排序方式: 共有3条查询结果,搜索用时 46 毫秒
1
1.
为了构建光学三极管模型,设计了一个基于半导体磁性材料InSb的PT(parity-time)对称耦合微腔的结构模型。通过结构参数优化,产生了PT对称结构磁场强耦合的极点效应。在极点频率附近,通过改变输入电流信号改变施加在磁性材料上的磁感应强度,实现极点状态下信号的放大输出。这种放大可以是同相,也可以是反相,该设计实现了特殊光学三极管模型。  相似文献   
2.
A titania support with a large surface area was developed, which has a BET surface area of 380.5 m2/g, four times that of a traditional titania support. The support was ultrasonically impregnated with 5 wt%vanadia. A special heat treatment was used in the calcination to maintain the large sur‐face area and high dispersion of vanadium species. This catalyst was compared to a common V2O5‐TiO2 catalyst with the same vanadia loading prepared by a traditional method. The new cata‐lyst has a surface area of 117.7 m2/g, which was 38%higher than the traditional V2O5‐TiO2 catalyst. The selective catalytic reduction (SCR) performance demonstrated that the new catalyst had a wid‐er temperature window and better N2 selectivity compared to the traditional one. The NO conver‐sion was>80%from 200 to 450 °C. The temperature window was 100 °C wider than the traditional catalyst. Raman spectra indicated that the vanadium species formed more V‐O‐V linkages on the catalyst prepared by the traditional method. The amount of V‐O‐Ti and V=O was larger for the new catalyst. Temperature programmed desorption of NH3, temperature programmed reduction by H2 and X‐ray photoelectron spectroscopy results showed that its redox ability and total acidity were enhanced. The results are helpful for developing a more efficient SCR catalyst for the removal of NOx in flue gases.  相似文献   
3.
本文以紫外-可见光谱、荧光光谱及黏度法研究了双马来腈二亚胺合铂与DNA的作用。紫外-可见光谱的研究表明,与DNA作用后,双马来腈二亚胺合铂在可见区的吸收显示出了减色效应,并伴随着吸收峰的蓝移。Scatchard图的分析结果表明,双马来腈二亚胺合铂与DNA的作用位点与溴化乙锭不同。黏度法实验表明,双马来腈二亚胺合铂与DNA作用后降低了DNA的相对黏度。这些研究结果表明,双马来腈二亚胺合铂以静电作用方式与DNA结合。本研究有助于深入理解双马来腈二亚胺合铂的作用机理并开发这种潜在的新型光动力治疗剂。  相似文献   
1
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号