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101.
以盐湖副产水氯镁石为原料,与一定比例的石灰反应得到氢氧化镁和氢氧化钙的混合沉淀物,该混合物经过滤、洗涤、烘干后在一定温度下煅烧得到符合皮江法炼镁用的合成煅白。实验结果表明,该工艺是可行的,在石灰/氯化镁摩尔比2.05~2.10:1,反应时间1.5,煅烧温度为800℃,煅烧时间为60min时,合成的煅白中钙镁摩尔比: 0.95~1.07:1,煅白的平均水活度达34%,符合硅热法炼镁用中间原料煅白的参数条件。该技术可为利用盐湖氯化镁制备金属镁新工艺开发提供了数据参考。 相似文献
102.
Evolving factor analysis is used to estimate the concentration profiles and spectra of Bi~(3 )and the bismuthchloride complexes BiCl~(2 )through BiCl_6~(3-)formed by injection of bismuth percblorate into a flowingstream of 1.0 mol l~(-1) HCl.The estimated spectra compare favorably with previously published spectraof the complexes. 相似文献
103.
Recharge patterns, possible flow paths and the relative age of groundwater in the Akaki catchment in central Ethiopia have been investigated using stable environmental isotopes δ18O and δ2H and radioactive tritium (3H) coupled with conservative chloride measurements. Stable isotopic signatures are encoded in the groundwater solely from summer rainfall. Thus, groundwater recharge occurs predominantly in the summer months from late June to early September during the major Ethiopian rainy season. Winter recharge is lost through high evaporation–evapotranspiration within the unsaturated zone after relatively long dry periods of high accumulated soil moisture deficits. Chloride mass balance coupled with the isotope results demonstrates the presence of both preferential and piston flow groundwater recharge mechanisms. The stable and radioactive isotope measurements further revealed that groundwater in the Akaki catchment is found to be compartmentalized into zones. Groundwater mixing following the flow paths and topography is complicated by the lithologic complexity. An uncommon, highly depleted stable isotope and zero‐3H groundwater, observed in a nearly east–west stretch through the central sector of the catchment, is coincident with the Filwoha Fault zone. Here, deep circulating meteoric water has lost its isotopic content through exchange reactions with CO2 originating at deeper sources or it has been recharged with precipitation from a different rainfall regime with a depleted isotopic content. Copyright © 2006 John Wiley & Sons, Ltd. 相似文献
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105.
The solubilities of ammonium chloride in aqueous ammonia decreased first and then increased with increasing ammonia concentrations, but the mechanism of this phenomenon has not been clarified. In the present work, the ATR-FTIR and Raman spectroscopy were employed to investigate the corresponding mechanism. The spectra analysis was focused on the region between 2500 and 4000 cm-1. It was firstly discovered that the N-H???N hydrogen bonds between ammonium ions and ammonia molecule was mainly formed in the NH4Cl-NH3-H2O system with concentrations higher than 10% ammonia, but N-H???O hydrogen bonds between ammonium ions and water molecule took advantage in the system with lower ammonia concentrations. Correspondingly, the phenomena of hydrogen bonding redshift and blueshift was observed respectively compared in NH3?H2O solution. Moreover, the hydrogen bonding structure of the saturated solution was obtained by means of MD simulation. The present work provides some theoretical basis for the separation of ammonium potassium chloride. 相似文献
106.
The results of a study evaluating the recharge/discharge conditions of an unconfined stressed granitic aquifer situated in a semi‐arid region of Andhra Pradesh, Southern India are presented. Over the last three decades, excessive withdrawal of groundwater has drastically lowered the water table to the bedrock. The watershed studied was divided into four zones based on geomorphology and hydrogeological conditions. Using environmental chloride data pertaining to groundwater, soil depth profiles, and some hydrogeologic and hydrochemical observations, a recharge model for the watershed was developed. The model revealed that the bulk of the vertical recharge in the western elevated land occurs through preferred pathways and that a small fraction occurs through the soil matrix. In addition, the watershed has a poor hydrogeologic fabric, as indicated by the small range of matrix flow recharge (1 to 1·5% of rainfall) among the four zones. The dominating preferential flow was high (~16% of the annual average rainfall) in the valley fills, but decreased to 5–5·5% in the plains. Furthermore, although the bulk of the recharge occurs vertically, considerable lateral movement of groundwater down the slope indicates that sequential hydrochemical changes occur. Distinct geomorphological features that exist in the watershed support the proposed model. Situations similar to those described above may exist in numerous watersheds in the granitic hard rock region; therefore, information obtained from investigations conducted in this watershed can aid in the development of plans enabling the sustainable exploitation of watersheds that have not yet been developed, as well as implementation of appropriate rainwater conservation measures in over‐exploited watersheds. Copyright © 2009 John Wiley & Sons, Ltd. 相似文献
107.
M. E. Sweeney C. L. Moore K. G. McQueen T. Spandler 《Australian Journal of Earth Sciences》2017,64(8):1085-1096
In Tasmania, most salts in the landscape originate from rainfall and accumulate in landscapes after evaporation occurs. The distribution and quantity of salt in rainfall from an array of bulk deposition collectors in the Greater Tamar Catchment were assessed for the period September 2013 to August 2014. The bulk deposition samples were analysed for pH, electrical conductivity, major ions (Ca, Mg, Na, SO4 and Cl) and a selection of trace ions. The average salt flux across the study area was 79 ± 10 kg/ha/yr region, ranging from 170 ± 12 kg/ha/yr near the coast in the north to 42 ± 6 kg/ha/yr inland. Deposition of most ions decreased from the northwest to the south and east, and peaked in winter and spring. Geomorphic factors such as elevation and topography have an important effect on the volume of rainfall and flux of salt from windblown dust and oceanic aerosols. A comparison of measured chloride and salt deposition in Tasmania with other Australian atmospheric studies indicates that continental-scale models of salt flux are not appropriate for Tasmania. New models are proposed that take into account the influence of the Southern Ocean, Tasman Sea and topographic variation in the study area. The results provide improved estimates of rainfall-derived salt inputs to catchments in northeast Tasmania and enable more accurate salt budget modelling. Improved understanding of volumes and distribution of salts has implications for the management of soils and infrastructure that degrade as a result of dryland salinity in Tasmania. 相似文献
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109.
M. L. Cox G. A. Sturrock P. J. Fraser S. T. Siems P. B. Krummel S. O'Doherty 《Journal of Atmospheric Chemistry》2003,45(1):79-99
There are large uncertainties in identifying and quantifying the natural and anthropogenic sources of chloromethanes – methyl chloride (CH3Cl), chloroform (CHCl3) and dichloromethane (CH2Cl2), which are responsible for about 15% of the total chlorine in the stratosphere. We report two years of in situ observations of these species from the AGAGE (Advanced Global Atmospheric Gas Experiment) program at Cape Grim, Tasmania (41° S, 145° E). The average background levels of CH3Cl, CHCl3 and CH2Cl2 during 1998–2000 were 551± 8, 6.3± 0.2 and 8.9± 0.2 ppt (dry air mole fractions expressed in parts per 1012) respectively, with a two-year average amplitude of the seasonal cycles in background air of 25, 1.1 and 1.5 ppt respectively. The CH3Cl and CHCl3 records at Cape Grim show clear episodes of elevated mixing ratios up to 1300 ppt and 55 ppt respectively, which are highly correlated, suggesting common source(s). Trajectory analyses show that the sources of CH3Cl and CHCl3 that are responsible for these elevated observations are located in coastal-terrestrial and/or coastal-seawater regions in Tasmania and the south-eastern Australian mainland. Elevated levels of CH2Cl2 (up to 70 ppt above background) are associated mainly with emissions from the Melbourne/Port Phillip region, a large urban/industrial complex (population 3.5 million) 300 km north of Cape Grim.Now at the Centre for Atmospheric ChemistryNow at School of Environmental Sciences 相似文献
110.
有机累托石的合成与特性研究 总被引:7,自引:0,他引:7
累托石是二八面体云母层与蒙脱石层1:1规间民支矿物,兼有云母和蒙脱三 某些特征。本文利用二甲基十八烷基羟乙基季铵盐与累托石进行阳离子交换反应合成有机累托石。并采用物理化学、X射线衍射、差热、热失重和红外吸收光谱等分析方法对它的特性进行了研究。经季铵盐复合处理后,累托放扣蒙脱石层间被有机阳离子覆盖,它的面网间距d001由原来的24.8°/A增至29.5°/A。累托石粘土亲水憎油性转变为憎水亲油性有机粘土后能在有机溶剂中膨胀和分散。它是一种有应用前景的新材料。 相似文献