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21.
铅在高岭石表面的解吸动力学   总被引:3,自引:0,他引:3  
经过酸性条件下(pH=3.1)Pb(Ⅱ)高岭石表面解吸动力学的研究,发现解吸反应与吸附反应动力学相似,也是一个二阶段的过程,即初始的快速解吸之后伴随着一个缓慢的释放过程。在快速解吸阶段,7min内解吸量即已达到41%。吸附铅没有完全解吸,有近38%残留在高岭石表面,即解吸和吸附过程不是完全可逆的。解吸过程可以用扩展Elovich方程、Elovich方程、双常数方程和一级扩散方程较好地似合。  相似文献   
22.
1 INTRODUCTION Extensive literature (Brown et al., 1985; Sawhney et al., 1981; Bierman and Swain, 1982; Connolly, 1980; Lopez-Avila and Hites, 1980; O扖onnor, 1988) described lots of sorbed pollutants or toxic substances in bed sediments of rivers, even after the effluent was halted for a long time. This is particularly true for hydrophobic organic compounds that can be sorbed on the particles and accumulated in the river bed sediments (Karickhoff et al., 1979). Pollution events of…  相似文献   
23.
The applications of calorimetric and ellipsometric methods to the understanding of adsorption phenomena occurring at the solid–liquid interface are presented with examples in the field of surfactant adsorption. The various experimental approaches are presented and compared, i.e., immersion calorimetry, titration calorimetry and liquid flow calorimetry. It is shown how they can be used to follow, in situ, the building steps of the surfactant adsorbed layer. On the other hand, ellipsometry allows the adsorption isotherm, the adsorption kinetics as well as the thickness of the adsorbed layer to be determined on well-defined flat surfaces. To cite this article: R. Denoyel, C. R. Geoscience 334 (2002) 689–702.  相似文献   
24.
萃淋树脂吸附法测金   总被引:5,自引:0,他引:5  
对萃淋树脂在酸性介质中吸附解脱金及相关体系的条件选择,以及萃淋树脂在生产方面的应用前景进行了实验研究。结果表明,萃淋树脂在稀王水介质中能较好地吸附金,用硫脲解脱金简便完全,检测限达0.002μg/g,吸附率达100%,解脱率99.8%。  相似文献   
25.
湍流混合动力学机理研究   总被引:7,自引:0,他引:7       下载免费PDF全文
在分析传统混合动力学机理基础上,通过宏观混合与微观混合时间量级的对比,提出了湍流条件下,涡流扩散主导宏观混合,分子扩散主导微观混合,而混合过程由宏观混合主导,欧拉数Eu可作为混合效果的控制指标,并通过3种不同容积反应器的混合搅拌试验,进一步证实了该指标的实用性。  相似文献   
26.
 The kinetics of the dehydroxylation of chrysotile was followed in situ at high temperature using real-time conventional and synchrotron powder diffraction (XRPD). This is the first time kinetics parameters have been calculated for the dehydroxylation of chrysotile. The value of the order of the reaction mechanism calculated using the Avrami model indicates that the rate-limiting step of the reaction is a one-dimensional diffusion with an instantaneous nucleation or a deceleratory rate of nucleation of the reaction product. Hence, the rate-limiting step is the one-dimensional diffusion of the water molecules formed in the interlayer region by direct condensation of two hydrogen atoms and an oxygen atom. The calculated apparent activation energy of the reaction in the temperature range 620–750 °C is 184 kJ mol−1. The diffusion path is along the axis of the fibrils forming the fibers. The amorphous or short-range ordered dehydroxylate of chrysotile is extremely unstable because forsterite readily nucleates in the Mg-rich regions. Moreover, it is less stable than the dehydroxylate of kaolinite, the so-called metakaolinite, which forms mullite at about 950 °C. This difference is interpreted in terms of the different nature of the two ions Mg2+ and Al3+ and their function as glass modifier and glass-forming ion, respectively. Received: 10 April 2002 / Accepted: 7 January 2003 Acknowledgements This work is part of a COFIN project (04 Scienze della Terra, NR 17, 2000) supported by MURST. Dr Dapiaggi is kindly acknowledged for help during the data collection at the Dipartimento di Scienze della Terra, University of Milan.  相似文献   
27.
The rate of the reversible homogeneous disproportionation of polysulfides was studied by following the optical absorbance of polysulfide solutions in a continuous plug flow reactor equipped with an on-line photometric detector. In order to avoid heterogeneous slow reactions involving sulfur colloids or precipitate, the reaction was initiated by an abrupt pH change from an undersaturated solution containing predominantly tetrasulfide species to a pH where pentasulfide is the dominant species. The disproportionation was found to follow first order reversible reaction dynamics. At environmentally relevant conditions the characteristic time of the disproportionation reaction is of the order of 10 s. This characteristic time implies that necessary conditions for speciation of the different polysulfide species by chromatography or another separation and subsequent quantification scheme should be of the order of 1 s.  相似文献   
28.
A multi-layer deposited ice film was prepared through water vapor deposition on a Ni plate in a vacuum chamber at 90 K, and was used as it was or after annealing at 140 K. NO2 was adsorbed as N2O4 approximately 90 K on the ice film prepared as above, and irradiated by 193 nm excimer laser light. The time-of-flight (TOF) spectra of the desorbed species, i.e., NO2, NO, O2 and O, were measured by a quadrupole mass spectrometer. The photochemical process obeyed an one-photon process. The relative yields of the products and their TOF spectra were dependent on the preparation condition of the ice film and also varied with the continuation of the laser irradiation. From the ice film annealed at 140 K, NO2, NO and O2 were desorbed with an approximate ratio of 1:1:0.01. From the non-annealed film, the relative yield of NO2 was much smaller than that of NO. The TOF spectrum of NO from the non-annealed ice film consisted of distinctly different two components corresponding to the 1700 and 100 K translational temperature, respectively. The fast component was lost when additional ice was deposited on the adsorbed N2O4. NO was supposed to be a predissociation product from the electronically excited NO2 prepared through the photodissociation of N2O4.  相似文献   
29.
南黄海盆地油气资源潜力一直是中国海上油气勘探关心的问题,但仍未取得突破性进展。生烃动力学研究对烃源岩生烃潜力评价至关重要,而该区古近系烃源岩的生烃动力学的研究十分薄弱。为此,在对南黄海盆地南部凹陷烃源岩常规地球化学分析统计基础上,着重选择南二凹低成熟样品开展PY-GC,SRA 和MSSV 等实验分析及动力学模拟。结果表明:南二凹阜四段烃源岩已进入生烃阶段,其产出的石油类型为石蜡-环烷-芳香基低蜡型,活化能分布范围为43~60 kcal/mol,其活化能主峰为51 kcal/mol,占72%,指前因子A=9.66×1012,生烃窗温度为128~158℃。该套烃源岩生烃历程中所生成的烃类在渐新世末期(23~30 Ma)以气液两相共存的形式存在,其余时期均以单一液相存在于该地层,至今转化率仍处于50%~60%。研究获得的南黄海盆地南二凹古近系泥岩的生烃动力学特征对于估算该盆地油气资源潜力极为重要,可为该区下一步油气勘探开发决策提供参考依据。  相似文献   
30.
Coexisting quartz, feldspar and biotite vary widely in their δ18O values and display a remarkable 18O/16O disequilibrium relation; especially, a quartz-feldspar reversal (△ 18OQUartz_feldspar< 0) exsists in the Aral granite pluton of the Altay Mountains, northern Xinjiang. The 18O / 16O exchange reaction definitely occurred between granite and water. Initial δ18O values of the granite and exotic fluid are evaluated by the mass balance consideration. The conventional method of discrimination between various magma derivations simply with δ18O values of either whole rock or separate minerals is misleading and unreliable. Experiments carried out by the authors show that the 18O / 16O exchange reaction is not accompanied by what geologists describe as petrological and mineralogical alteration effect. This decoupling relation implies that exchange reaction occurs at a relatively high temperature during subsolidus-postmagmatic cooling of magmas. The exchange mechanism is mainly diffusion-controlled. It is  相似文献   
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