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   23篇
  免费   1篇
  国内免费   5篇
化学   22篇
力学   2篇
数学   1篇
物理学   4篇
  2024年   1篇
  2023年   2篇
  2022年   1篇
  2021年   1篇
  2020年   2篇
  2019年   5篇
  2018年   2篇
  2015年   1篇
  2013年   4篇
  2012年   4篇
  2011年   2篇
  2009年   1篇
  2005年   1篇
  1999年   1篇
  1993年   1篇
排序方式: 共有29条查询结果,搜索用时 31 毫秒
1.
In geomagnetic field, a series of tensile experiments on the low-carbon steel sticks were carried out. A special homemade detector was used to measure the magnetic gradient on the material surface. The results showed that the relationship between the magnetic gradient and the stress varied with different conditions of measurement. There was no obvious correlation between the magnetic gradient and the tensile stress if the sample remained on the material test machine. If the sample was taken off from the machine, the measured magnetic gradient was linear with the prior maximum stress. In Nanjing, PR China, a place of 32°N latitude, the slope of the linear relationship was about 67 (uT/m)/MPa. This offered a new method of non-destructive stress testing by measuring the magnetic gradient on the ferromagnetic component surface. The prior maximum applied stress of the sample could be tested by measuring the present surface magnetic gradient. Actually this phenomenon was the metal magnetic memory (MMM). The magnetic gradient near the stress concentration zone of the sample, the necking point, was much larger than other area. Thus, the hidden damage in the ferromagnetic component could be detected early by measuring the magnetic gradient distribution on its surface. In addition, the magnetic memory signal gradually weakened as the sample was taken off and laid aside. Therefore, it was effective for a given period of time to detect the stress or stress concentration based on the MMM testing.  相似文献   
2.
Summary of main observation and conclusion An efficient and organic ligand-free heterogeneous catalytic system for hydroformylation of olefins is highly desirable for both academy and industry.In this study,simple Rh black was employed as a heterogeneous catalyst for hydroformylation of olefins in the absence of organic ligand.The Rh black catalyst showed good catalytic activity for a broad substrate scope including the aliphatic and aromatic olefins,affording the desired aldehydes in good yields.Taking the hydroformylation of ethylene as an example,86%yield of propanal and TOF of 200 h-1 were obtained,which was superior to the reported homogeneous catalytic systems.In addition,the catalyst could be reused five times without loss of activity under identical reaction conditions,and the Rh leaching was negligible after each cycle.  相似文献   
3.
二氧化碳是碳资源利用的最终形式,也是一种绿色的碳一资源。通过催化化学的方法将二氧化碳转化为高附加值精细化学品是二氧化碳循环利用的有效途径。酰胺类化合物是一类重要的化工原料和溶剂,广泛应用于医药、农药、日用化学品及石油化工等众多领域且需求量巨大。因此,以二氧化碳为羰源,通过高效催化体系的建立实现二氧化碳与胺反应合成甲酰胺具有重要意义。本文分别从催化体系、还原剂和反应机理等角度综述了这一领域近年来的主要研究成果。其中,催化体系可分为贵金属催化剂如Ir、Pd、Pt、Ru、Rh,非贵金属催化剂如Ni、Mo、Cu、Fe、Co、Zn、Al,有机分子催化剂和无催化剂体系,常用的还原剂为H2,硅烷和硼烷。在此基础上,对不同催化体系的典型反应机理进行了讨论。  相似文献   
4.
Olivine LiFePO4/C nanocomposite cathode materials with small-sized particles and a unique electrochemical performance were successfully prepared by a simple solid-state reaction using oxalic acid and citric acid as the chelating reagent and carbon source. The structure and electrochemical properties of the samples were investigated. The results show that LiFePO4/C nanocomposite with oxalic acid (oxalic acid: Fe2+= 0.75:1) and a small quantity of citric acid are single phase and deliver initial discharge capacity of 122.1 mAh/g at 1 C with little capacity loss up to 500 cycles at room temperature. The rate capability and cyclability are also outstanding at elevated temperature. When charged/discharged at 60 °C, this materials present excellent initial discharge capacity of 148.8 mAh/g at 1 C, 128.6 mAh/g at 5 C, and 115.0 mAh/g at 10 C, respectively. The extraordinarily high performance of LiFePO4/C cathode materials can be exploited suitably for practical lithium-ion batteries.  相似文献   
5.
刚体元方法是研究块体系的变形和运动的一种数值方法,可以用它来研究弹塑性物体的极限平衡问题,文中用通用的二维刚体元程序计算了正方形柱体顶面中心区域作用方形基础载荷情况的上限解,结果表明,这种方法较好的精度和广泛的适用性。  相似文献   
6.
氯霉素全抗原的合成与鉴定   总被引:14,自引:0,他引:14  
采用戊二醛法和羰基二咪唑法,将半抗原氯霉素(CAP)与载体牛血清白蛋白(BSA)偶联,制得氯霉素全抗原CAP-BSA,并由紫外光谱和红外光谱确定偶联成功。所合成抗原的聚丙烯酰胺凝胶电泳(SDS)只见一条区带,表明所合成的氯霉素与BSA偶联物可以作为免疫抗原。用市售的氯霉素快速检测试剂盒可以定量测定所合成抗原中氯霉素的含量。将固体配成1mg/mL液,用TNBS法测氨基酸残基,得到BSA上偶联的氯霉素数目。  相似文献   
7.
8.
High-performance catalysts sufficient to significantly reduce the energy barrier of water activation are crucial in facilitating reactions that are restricted by water dissociation. Herein we present a Cu−Co double-atom catalyst (CuCo-DAC), which possesses a uniform and well-defined CuCoN6(OH) structure, and works together to promote water activation in silane oxidation. The catalyst achieves superior catalytic performance far exceeding that of single-atom catalysts (SACs). Various functional silanes are converted into silanols with up to 98 % yield and 99 % selectivity. Kinetic studies show that the activation energy of silane oxidation by CuCo-DAC is significantly lower than that of Cu single-atom catalyst (Cu-SAC) and Co single-atom catalyst (Co-SAC). Theoretical calculations demonstrate two different reaction pathways where water splitting is the rate-determining step and it is accelerated by CuCo-DAC, whereas H2 formation is key for its single-atom counterpart.  相似文献   
9.
An efficient dimedone‐catalyzed synthesis of highly functionalized thiazol‐2‐yl substituted E‐acrylonitrile derivatives has been established through two‐step reaction of α‐thiocyanate ketones with malononitrile and amines. The α‐thiocyanate ketones were subjected with malononitrile to provide thiazol‐2‐ylidenemalononitrile derivatives, followed with various amines in the present of dimedone to yield the final thiazol‐2‐yl substituted acrylonitrile derivatives.  相似文献   
10.
研制一套同时具有时间分辨及空间分辨能力的超快电子衍射(UED)系统,理论时间分辨能力达到300 fs,空间分辨能力160 lp/mm,并对该系统进行了静态性能分析。实验表明,优化后系统电子束直径约为300 m,电子打靶角度约为0.09,同时对x和y偏转板的灵敏度、电子束斑尺寸及位置稳定性进行定量分析,利用该系统进行多晶铝膜电子衍射实验,分析衍射图样表明系统最小可以分辨单个晶格间距的0.36%。  相似文献   
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