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   108篇
  免费   1篇
  国内免费   3篇
电工技术   25篇
综合类   7篇
化学工业   5篇
金属工艺   12篇
机械仪表   4篇
矿业工程   1篇
能源动力   14篇
轻工业   3篇
水利工程   4篇
石油天然气   1篇
武器工业   1篇
无线电   13篇
一般工业技术   8篇
冶金工业   4篇
自动化技术   10篇
  2024年   1篇
  2022年   1篇
  2021年   3篇
  2020年   3篇
  2019年   1篇
  2018年   1篇
  2017年   3篇
  2015年   3篇
  2014年   9篇
  2013年   6篇
  2012年   8篇
  2011年   18篇
  2010年   8篇
  2009年   5篇
  2008年   11篇
  2007年   8篇
  2006年   5篇
  2005年   3篇
  2004年   1篇
  2003年   3篇
  2001年   3篇
  2000年   3篇
  1999年   1篇
  1997年   1篇
  1996年   2篇
  1991年   1篇
排序方式: 共有112条查询结果,搜索用时 0 毫秒
1.
本文介绍了汽轮机监视装置和瞬态数据管理一体化系统在某发电厂300MW等级汽轮机上运行中,几个典型故障的诊断实例。  相似文献   
2.
基于TSI568的RapidIO交换模块设计   总被引:1,自引:0,他引:1  
RapidIO互连构架是一个开放的标准,可应用于连接多处理器、存储器和通用计算平台.本文简要介绍了基于Tundra公司T5I568芯片的RapidIO交换模块的设计原理和实现方法,并对一些关键技术进行介绍.  相似文献   
3.
为了提高TC4合金的耐磨性能,采用激光热喷涂技术在其表面制备了Co30Cr8W1.6C3Ni1.4Si涂层。通过扫描电子显微镜(SEM)和X射线衍射(XRD)分析了涂层的形貌和物相,并通过摩擦磨损实验研究了涂层在PAO+2.5% MoDTC(质量分数)油中的磨损行为。结果表明,激光热喷涂的Co30Cr8W1.6C3Ni1.4Si涂层主要由Ti、WC1-x、CoO、Co2Ti4O和CoAl相组成,在涂层界面形成冶金结合。在激光功率为1000、1200和1400 W时所制备的涂层平均摩擦因数分别为0.151、0.120和0.171,其对应的磨损率分别为1.17×10-6、1.33×10-6和2.80×10-6 mm3?N-1?m-1,磨损机理为磨粒磨损,其枝晶尺寸对降磨起主要作用。  相似文献   
4.
结合华能辛店发电厂200MW机组汽轮机监视仪表系统(TSI)改造的情况,介绍了MMS 6O0O系统的配置及系统特点,对TSI改造中遇到的问题及解决方法进行了总结和分析。  相似文献   
5.
首次提出了N,N-二氯二甲基对苯二胺一H2O2-HRP光度法测定HRP的方法。HRP催化H2O2氧化N,N-二氯二甲基对苯二胺生成有色化合物,通过测定有色化合物在λmax=553.6nm处的吸光光度值,间接测定HRP的含量。在所选定的实验条件下,HRP的线性范围为1.0×10-10~1.0×10-8g/mL,本法用于游离HRP的测定,与经典的ELISA显色光度法相比,灵敏度提高了一个数量级。HRP的检测限为5.1×10-11g/mL。  相似文献   
6.
J2EE平台上消息驱动Bean对客户的响应与回传的实现   总被引:1,自引:0,他引:1  
EJB是基于Java的服务器端组件架构技术,借助于EJB,开发者能够轻松构建企业的、分布式组件应用,并且能够开发架构灵活、运行可靠及安全的应用系统.在EJB规范中,客户可向中间件发送消息,而消息驱动Bean(MDB)能从中间件接收消息,从而客户与消息驱动Bean实现异步传输消息,形成松耦合的状态.介绍了消息发布客户与消息驱动Bean通过服务器互传消息的理论,给出了Java消息服务的请求/响应解决方案,并且在J2EE1.4平台上实现了消息驱动Bean将响应结果异步回传给生产消息的客户,而客户可以是应用程序,Servlet/JSP,或EJB本身.  相似文献   
7.
Photochemical decomposition of nilvadipine (NV), a derivative of 1,4-dihydropyridine (DHP), was studied. Photodegradation was carried out in the conditions recommended in the first version of the document issued by the International Conference on Harmonization (ICH), currently in force in the studies of photochemical stability of drugs and therapeutic substances. Methanol solutions of NV were irradiated with a high-pressure mercury arc lamp, type HBO 200 (300–400 nm). The maximum absorption of radiation at 365 nm was achieved by applying the interference filter and Wood's filter. The assessment of NV photodegradation was made on the basis of the UV spectrophotometric and high-performance liquid chromatographic (HPLC) methods. Quantitatively, the process was described with the calculated rate constants of decomposition k, time of decomposition of 50% of the compound t0.5, and time of decomposition of 10% of the compound t0.1. The two methods applied allowed a determination of the kinetic parameters of NV photodegradation from the relationship ln c = f(t). Using the Reinecke salt as a chemical actinometer, apparent quantum yields of photodegradation were obtained; after extrapolation to the time of irradiation zero, these gave the actual quantum yield (Φ = 7.3 · 10?5). The quantum yield of fluorescence at λexc = 375 nm was about 9.3 · 10?4. The methods used for evaluation of NV photodegradation were subjected to validation, and results of the analytical methods were statistically assessed by Snedecor F and Student t tests. The former test revealed no statistically significant difference between the variances obtained by the HPLC and UV spectrophotometric methods. Also, verification of the zero hypothesis of the Student t test on equality of means of the results obtained gave no significant differences between the two methods.  相似文献   
8.
Samples with nominal composition RuSr2Sm1.4Ce0.6Cu2O10−δ were synthesized at different conditions and their magnetic and superconducting properties were investigated. It was established that the magnetic order is of a long range type. It was shown that the increase of the oxygen content and the presence of larger microcrystals enhance the temperature of the onset of diamagnetism and the diamagnetic volume fraction of the samples, but do not significantly affect the temperatures of the intragrain superconducting and ferromagnetic transitions.  相似文献   
9.
The cyclopentadiene/cyclopentadienyl system forms a critical part in the oxidation chemistry of aromatic fuel components used in surrogate fuels and the importance of the cyclopentadienyl radical in poly-aromatic hydrocarbon (PAH) growth has also been noted due to its site dependent reactivity. The latter aspect has been subject to a number of studies along with the initial pyrolysis steps. By contrast, few studies have been performed of the corresponding oxidation chemistry under conditions of relevance to combustion applications. Thermochemical data for oxidation reactions featuring the cyclopentadienyl radical with O, OH, HO2 and O2 were determined at the G3B3 and G4/G4MP2 levels in combination with an analysis of internal rotations using density functional theory and with the Jahn–Teller effect treated as a pseudo-rotation. The calculated potential energy surfaces were subsequently used in a consistent manner for the determination of pressure dependent reaction rate parameters through the Rice–Ramsperger–Kassel–Marcus/master-equation approach with Eckart quantum tunnelling corrections applied to reactions involving hydrogen transfers. The accuracy of the method was further investigated by comparisons of computed rate parameters for pyrolysis reactions with alternative determinations. The resulting chemistry was incorporated into an evaluation framework for the study of cyclopentadiene oxidation using recent experimental flow reactor data and principal uncertainties in reaction pathways assessed.  相似文献   
10.
采用高温固相两步法制备了两种Li1.4M0.4Ti1.6(PO4)3(M=Al、Cr)系列NASICON功能材料,对不同掺杂合成的样品进行了XRD和SEM表征,并分别对其Na+的交换吸附容量进行了测定。结果表明,对LiTi2(PO4)3掺入适量的Al3+和Cr3+后未改变其晶体结构,合成的吸附剂粒径分布在5~10μm;Li1.4M0.4Ti1.6(PO4)3(M=Al、Cr)对Na+有特效吸附作用,当pH=11.0时,Li1.4Al0.2Cr0.2Ti1.6(PO4)3的饱和交换吸附容量可达69.26mg/g。  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