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11.
Yongfeng JIA Xin WANG George Demopoulos 《中国地球化学学报》2006,25(B08):35-35
Adsorption of arsenate on hydrous iron oxide is an important process controlling geochemical cycling of arsenic in environment as well as the fate of arsenic-bearing mining wastes. The widely accepted view on the mechanism of adsorption is that arsenate is adsorbed via bidentate binuclear inner-sphere complexation. In this study, we characterized the arsenate-hydrous iron oxide sorption solids synthesized at pH=3-8 using Fourier transformed infrared spectroscopy (FTIR) and X-ray diffraction (XRD). It has been determined that poorly crystalline ferric arsenate developed on the surface of iron oxide when arsenate was sorbed at acidic pH, while at alkaline pH the adsorption of arsenate was via bidentate complexation. 相似文献
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13.
采用微波消解-硼酸络合-火焰原子吸收光谱法测定石英砂中的氧化钙和氧化镁。样品在MK-Ⅲ型实验室微波炉上消解,消解压力为2.0 MPa、消解时间为5 m in,以硼酸络合消除氢氟酸的影响。方法已用于实际样品的测定,7次测定的相对标准偏差(RSD)小于5%,加标回收率为95.0%~104.2%。 相似文献
14.
Sandra Andrade Raphael HypolitoHorstpeter H.G.J. Ulbrich Marinês L. Silva 《Chemical Geology》2002,182(1):85-89
The determination of FeO of geologic materials by modern instrumental methods (such as atomic absorption spectroscopy (AAS), inductively coupled plasma atomic emission spectroscopy (ICP-AES), X-ray fluorescence (XRF), etc.) cannot distinguish between different oxidation states of elements. In many cases, the oxidation state of Fe has to be known in order to perform several chemical calculations (norms, etc.) and discuss the reactions that occur during weathering, hydrothermal alteration and other processes. A modified Wilson method is proposed, giving reproducible results in a much shorter time than the classical method. Back-titration with potassium dichromate and an Fe(II) and ammonia sulphate solution is used, after dissolution of the sample powder in a heated HF/H3PO4 mixture and an ammonium vanadate solution. This modified method, tested with several international reference materials, gives reliable results, equivalent to the ones cited in the literature for the reference materials. 相似文献
15.
L. Kristensen C. E. Andersen H. E. Jørgensen P. Kirkegaard K. Pilegaard 《Journal of Atmospheric Chemistry》1997,27(3):249-269
We have discussed the behavior of a non-conserved scalar in the stationary, horizontally homogeneous, neutral surface-flux layer and, on the basis of conventional second-order closure, derived analytic expressions for flux and for mean concentration of a gas, subjected to a first-order removal process. The analytic flux solution showed a clear deviation from the constant flux, characterizing a conserved scalar in the surface-flux layer. It decreases with height and is reduced by an order of magnitude of the surface flux at a height equal to about the typical mean distance a molecule can travel before destruction. The predicted mean concentration profile, however, shows only a small deviation from the logarithmic behavior of a conserved scalar. The solution is consistent with assuming a flux-gradient relationship with a turbulent diffusivity corrected by the Damköhler ratio, the ratio of a characteristic turbulent time scale and the scalar mean lifetime. We show that if we use only first-order closure and neglect the effect of the Damköhler ratio on the turbulent diffusivity we obtain another analytic solution for the profiles of the flux and the mean concentration which, from an experimental point of view, is indistinguishable from the first analytic solution. We have discussed two cases where the model should apply, namely NO which, by night, is irreversibly destroyed by interaction with mainly O3 and the radioactive 220Rn. Only in the last case was it possible to find data to shed light on the validity of our predictions. The agreement seemed such that a falsification of our model was impossible. It is shown how the model can be used to predict the surface flux of 220Rn from measured concentration profiles. 相似文献
16.
本文提出了用ICP-AES法直接同时测定高纯氧化钇中14个稀土和16个非稀土杂质元素的分析方法,对被测元素的 谱线、氧化钇基本及背景影响进行了研究,用标准加入法测出氧化钇基准中的微量杂质元素,消除了由于忽略基准中的杂质元素含量给高纯氧化钇分析测定带来的误差,同时对工作条件进行了优化。方法中各被测元素的检出限为0.003~1.31ug/g,能够满足生产过程中的质量控制及进出口商品检验 相似文献
17.
湘西南区氧化锰矿以锰帽型氧化锰矿为主,赋矿地层为震旦系下统湘锰组。其特点是含锰点多,分布面广,矿体在地壳贫化,往下3~7m开始富集,氧化深度40m左右。 相似文献
18.
西昆仑山南侧甜水海湖岩芯铁变化的环境记录 总被引:11,自引:0,他引:11
阐述了青藏高原西昆仑山南侧甜水海湖岩芯沉积物中氧化铁的丰度、频率分布和富集系数的变化规律。其丰度值范围FeO0.39%-3.95%,平均值为1.25%;Fe2O30.44%-8.09%,平均值为2.60%;Fe2O3/FeO0.21-3.60,平均比值1.12。说明该彻岩芯沉积物中铁平均丰度值较低,但其变化幅度较宽且清楚,在一定程度上反映了古气候环境具有较大幅度的波动。变异系数值表明,该湖岩芯沉积物中FeO的离散程度较Fe2O3大。大约距今23万年来氧化铁的沉积地球化学特征可划分出7个环境演化阶段,并基本上可与深海氧同位索阶段对比。揭示了甜水海湖演化与青藏高原强烈隆升引起的气候环境改变的密切关系。在距今23一15万年,沉积以河流相或冲积、洪积相为主,沉积环境以氧化环境为主导,气候以温干型波动;在距今15-7.4万年,沉积以湖相为主,沉积环境以还原环境为主导,气候以温湿型为主;在距今74万年以来,湖盆沉积环境多样化,沉积物以湖相和近源冲积、洪积相交替出现。气候出现冷湿、冷干、温湿和温干多种波动模式。这些资料分析初步认为甜水海古湖大约形成于距今15万年,即青藏高原第三成湖期,这也与青藏高原在距今15万年左右的再次构造隆升有关。 相似文献
19.
通过对碳酸锰氧化实验的结果分析和讨论,建立了一种适合于锰氧化过程的非平衡热力学模型,并利用此模型对硫酸锰氧化过程作了热力学可行性分析,研究结果表明,碳酸锰氧化过程是矿物组合的变化过程,也是锰自身价态的转为过程,整个过程既存在平衡状态,又存在非平衡状态,是一个不可逆的,多相的复杂反应。 相似文献
20.
Magneticmineralsintheloess paleosolseriesaccountforabout 1 % -2 %ofthetotal (LiuTungshengandZhangZhonghu ,1 962 ) .Duetotheiraerolianorigin ,themagneticmineralsarecomplicatedincomposition ,largeingrainsizerange ,andsignificantlydifferentincrystallinity .Asaresult,researchonthesemagneticmineralswouldbesetwithalotofdifficulties.Previousre searchersemployedopticalmicroscopic ,X raydiffractionandM ssbauerspectrometrictechniquestostudythemagneticmineralsintheloess paleosolseries,andchieflyontheb… 相似文献