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131.
随着对汽车安全性以及舒适性要求的提高,汽车厂商对于负载模拟系统的动态响应和控制精度也有了更高的要求。在电机控制系统中,参数的突变会引起试验台的稳定性降低并且伴有震荡产生。为克服震荡,文中使用伺服控制液压马达模拟EPS的方向盘系统以及负载系统代替原有的电机控制。通过Simulink仿真得到的系统阶跃响应图和Bode图分析发现,该试验台液压系统闭环稳定,且在一定程度上克服了震荡现象,具有可借鉴性。 相似文献
132.
二维液相色谱(2D-LC)因具有较高的峰容量,在复杂样品的分离分析中获得了广泛的关注。然而,制备型2D-LC以纯化高纯单体为目标,在方法开发和设备构成等方面与分析型2D-LC有较大的不同,目前尚未得到充分的开发,在大规模的制备纯化中应用较少。本文以一套制备液相色谱模块为分离系统,以稀释泵、切换阀和捕集柱阵列为接口,构建了新型的制备型2D-LC系统,旨在规模化纯化多个活性成分。以烟叶中可以用作医药原料的烟碱、绿原酸、芦丁和茄尼醇等组分为目标物,考察了不同类型填料对样品的捕集效率、过载条件下的色谱保留行为等,优化了制备色谱条件。进而利用在线2D-LC系统实现了烟叶提取物的纯化,通过一次运行获得了4个高纯化合物。该系统具有中压色谱纯化成本低、系统在线运行自动化程度高、稳定性好及容易放大等优点。烟叶中活性化学成分的回收利用对促进烟草行业的发展及带动地方农业经济开发具有重大的意义。 相似文献
133.
新型两性聚电解质高吸水性树脂CMCTS-g-(PAA-co-PTMAAC)的制备研究 总被引:2,自引:0,他引:2
通过氧化还原引发荆引发的接枝共聚反应,使阴离子型单体丙烯酸(AA)和阳离子型单体三甲基烯丙基氯化铵(TMAAC)在羧甲基壳聚糖(CMCTS)的分子链上接枝共聚,制得羧甲基壳聚糖接枝-(聚丙烯酸-co-聚三甲基烯丙基氯化铵)(CMCTS-g-(PAA-co-PTMAAC)两性聚电解质高吸水性树脂.采用红外光谱对产物的结构进行了表征,比较了反应条件对产物吸液性能的影响.发现制备具有良好吸液性能的高吸水性树脂的最优化反应条件为:TMAAC占单体总质量的14.3%,mNNMBA/mAA值在0.014附近,单体总质量为CMCTS质量的9.33倍,丙烯酸中和度在20%~30%之间.研究发现,随外部溶液pH值的变化,两性聚电解质高吸水性树脂的溶胀性能在酸性和碱性条件下各有一个最大值,在等电点处产物的吸液性相对较低. 相似文献
134.
135.
136.
Adsorbed para-nitrophenol on HDTMAB organoclay--a TEM and infrared spectroscopic study 总被引:1,自引:0,他引:1
para-Nitrophenol adsorbed on hexadecyltrimethylammonium bromide modified montmorillonite has been studied using a combination of X-ray diffraction TEM and infrared spectroscopy. Upon formation of the organoclay, the properties change from hydrophilic to hydrophobic. It is proposed that para-nitrophenol is adsorbed onto the water in the cation hydration sphere of the organoclay. As the cation is replaced by the surfactant molecules the para-nitrophenol replaces the surfactant molecules in the clay interlayer. Significant changes in the water vibrations occur in this process. Bands attributed to CH stretching and bending vibrations in general decrease as the concentration of the surfactant (CEC) increases up to 1.0 CEC. After this concentration the bands increase approaching a value the same as that of the surfactant. Strong changes occur in the HCH deformation modes of the methyl groups of the surfactant. These changes are attributed to the methyl groups locking into the siloxane surface of the montmorillonite. Such a concept is supported by changes in the SiO stretching bands of the montmorillonite siloxane surface. This study demonstrates that para-nitrophenol will penetrate into the untreated clay interlayer and replace the intercalated surfactant in surfactant modified clay, resulting in the change of the arrangement of the intercalated surfactant. 相似文献
137.
Water purification is of extreme importance worldwide. p-Nitrophenol was used as a test chemical to design and test an organoclay for the removal of p-nitrophenol from an aqueous solution. Synthesis of the organoclay with methyltrioctadecylammonium bromide [CH(3)(CH(2))(17)](3)NBr(CH(3)) labeled as MTOAB results in multiple expansions of the montmorillonite clay from 1.24 nm to a maximum of 5.20 nm as is evidenced by the XRD patterns. Thermal analysis shows strong bonding of the surfactant to the clay siloxane layers and the interaction of the p-nitrophenol with the clay surfaces. It is proposed that the p-nitrophenol penetrates the siloxane layer of the clay and bonds through the ditrigonal space of the siloxane hexagonal units to the inner OH units. Such a concept is supported by the observation of an additional infrared band at 3652 cm(-1) for the organoclay. Shifts in the p-nitrophenol OH stretching vibrations mean a strong interaction of the p-nitrophenol molecule. Significant changes in the siloxane stretching bands are also observed. 相似文献
138.
Surfaces of a Wyoming SWy-2 sodium montmorillonite were modified using microwave radiation through intercalation with the cationic surfactants octadecyl-trimethyl ammonium bromide, dimethyldioctadecylammonium bromide, and methyl-tri-octadecyl ammonium bromide by an ion exchange mechanism. Changes in the surfaces and structure were characterized using X-ray diffraction (XRD), thermal analysis (TG) and infrared (IR) spectroscopy. Different configurations of surfactants within montmorillonite interlayer are proposed based on d(001) basal spacings. A range of surfactant molecular environments within the surface-modified montmorillonite are proposed based upon their thermal decomposition. IR spectroscopy using a smart endurance single bounce diamond attenuated total reflection (ATR) cell has been used to study the changes in the spectra of CH asymmetric and symmetric stretching modes of the surfactants to provide more information of the surfactant molecular configurations. 相似文献
139.
Caoshui Xiong Li Pi Yeqing Tang Hong Zhu Denggang Zong Junfeng Zhang Yunfei Deng Jingsheng Zhu Yuheng Zhang 《中国科学A辑(英文版)》1999,42(1):106-112
The La0,67Sr0.33Mn03 +δ/Pr0.7Cao.3Mn03+δ/La0.67Sr0.33Mn03+δ(LPL) trilayered films on (100)LaA-1O3 substrates are prepared by using direct current (DC) magnetron sputtering method. The results obtained by means of X-ray
powder diffractometer show that all films are the high quality epitaxial films. The results gained by SQUID magnetometer indicate
that there is a magnetic coupling in the LPL trilayered films. The resistivities of LSMO, PC-MO and LPL films are measured
using standard four-probe method and analyzed logp-1/T curve. From the results it is concluded that the middle-layered PCMO which is ferromagnetic may play a role of intra-magnetic
field, which weakens the paramagnetism of LSMO film, lowersp
max and enlargesT
p
which is the transition temperature from metal to insulator, just as the applied magnetic field does. And the middle-layered
PCMO may induce the change of the density of states in the LSMO’s gap. The two reasons above make the resistivity andT
p
of the samples in zero field change with the thickness of PCMO layers.
Project supported by the Chinese Academy of Sciences and the Foundation of State Science and Technology Commission of China. 相似文献
140.
常规X射线成象技术是建立在吸收衬度和几何光学基础上.介绍了“in-line”位相衬度成象 技术和成象理论.以生物样品为例,说明常规X射线吸收衬底成象与位相衬度成象的差别,并 对X射线源尺寸对成象衬度的影响进行了研究.此外,对吸收衬底象和位相衬度象的关键参量 进行了计算模拟和讨论.
关键词:
位相衬度
成象
硬X射线 相似文献