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排序方式: 共有439条查询结果,搜索用时 15 毫秒
1.
由共聚法制得的铁铝复合交联剂交换钠基蒙脱石层间的水合钠离子,再经SO42-改性处理制备了铁铝复合层柱粘土固体超强酸催化剂.利用xRD、FT-IR和BET法对催化剂的结构进行了表征.以乙酸正丁酯的合成反应为探针反应对催化剂的活性进行了测试.通过正交实验确定了铁铝复合交联粘土SO42-改性最佳工艺条件.研究了催化剂对探针反应的选择性及重复使用情况.结果表明:在由实验确定的最佳改性工艺条件下,乙酸的转化率达92.2%,反应中无副产物产生,催化剂具有较好的重复使用性能. 相似文献
2.
太平洋中部表层沉积物镁铝含量比的变化 总被引:4,自引:0,他引:4
本文根据中、日调查资料,研究了太平洋中部表层沉积物镁铝含量比的变化,并探讨其影响因素。 相似文献
3.
Lateral moraines constructed along west to east sloping outlet glaciers from mountain centred, pre-last glacial maximum (LGM) ice fields of limited extent remain largely preserved in the northern Swedish landscape despite overriding by continental ice sheets, most recently during the last glacial. From field evidence, including geomorphological relationships and a detailed weathering profile including a buried soil, we have identified seven such lateral moraines that were overridden by the expansion and growth of the Fennoscandian ice sheet. Cosmogenic 10Be and 26Al exposure ages of 19 boulders from the crests of these moraines, combined with the field evidence, are correlated to episodes of moraine stabilisation, Pleistocene surface weathering, and glacial overriding. The last deglaciation event dominates the exposure ages, with 10Be and 26Al data derived from 15 moraine boulders indicating regional deglaciation 9600 ± 200 yr ago. This is the most robust numerical age for the final deglaciation of the Fennoscandian ice sheet. The older apparent exposure ages of the remaining boulders (14,600-26,400 yr) can be explained by cosmogenic nuclide inheritance from previous exposure of the moraine crests during the last glacial cycle. Their potential exposure history, based on local glacial chronologies, indicates that the current moraine morphologies formed at the latest during marine oxygen isotope stage 5. Although numerous deglaciation ages were obtained, this study demonstrates that numerical ages need to be treated with caution and assessed in light of the geomorphological evidence indicating moraines are not necessarily formed by the event that dominates the cosmogenic nuclide data. 相似文献
4.
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6.
新疆十红滩砂岩型铀矿床基本特征及成因分析 总被引:29,自引:9,他引:29
新疆十红滩铀矿床是中国近年发现的层间氧化带型砂岩铀矿床。该矿床位于吐鲁番—哈密盆地西南部的艾丁湖斜坡带西侧,赋矿地层为中侏罗统西山窑组辫状河—曲流河相的含煤碎屑岩系;矿体严格受发育于河道砂体中的层间氧化带前锋线控制,矿体形态呈卷状或板状;含矿岩石主要为灰—深灰色疏松和次疏松细—粗粒长石石英砂岩,铀主要以吸附形式存在;全岩Pb同位素测定的主成矿年龄为24 Ma。研究认为:晚侏罗世后,持续干热气候条件下,层间氧化带的充分发育,高含氧水在富铀地层砂体中持续向前运移,在富还原剂地球化学障形成铀沉淀富集,是该铀矿床的成因。 相似文献
7.
8.
柱撑粘土矿物层间域的性质及其环境意义 总被引:10,自引:3,他引:10
柱撑粘土矿物是近年来胺国内外矿物学广泛关注的矿物材料之一。柱撑粘土矿物层间域是一个特殊的化学反应场所。本系统评述了氮氧化物、重金属离子、阴离子、肥料养分及有机污染物等环境污染物在柱撑粘土矿物层间域中的催化还原、吸附、脱附、控释及光催化反应机理,着重阐述了柱撑粘土矿物的层间域性质,讨论了它们的环境化学行为对环境的影响和意义。 相似文献
9.
I. E. Paukov N. K. Moroz Yu. A. Kovalevskaya I. A. Belitsky 《Physics and Chemistry of Minerals》2002,29(4):300-306
The heat capacity of paranatrolite and tetranatrolite with a disordered distribution of Al and Si atoms has been measured
in the temperature range of 6–309 K using the adiabatic calorimetry technique. The composition of the samples is represented
with the formula (Na1.90K0.22Ca0.06)[Al2.24Si2.76O10]·nH2O, where n=3.10 for paranatrolite and n=2.31 for tetranatrolite. For both zeolites, thermodynamic functions (vibrational entropy, enthalpy, and free energy function)
have been calculated. At T=298.15 K, the values of the heat capacity and entropy are 425.1 ± 0.8 and 419.1 ±0.8 J K−1 mol−1 for paranatrolite and 381.0 ± 0.7 and 383.2 ± 0.7 J K−1 mol−1 for tetranatrolite.
Thermodynamic functions for tetranatrolite and paranatrolite with compositions corrected for the amount of extraframework
cations and water molecules have also been calculated. The calculation for tetranatrolite with two water molecules and two
extraframework cations per formula yields: C
p
(298.15)=359.1 J K−1 mol−1, S(298.15) −S(0)=362.8 J K−1 mol−1. Comparing these values with the literature data for the (Al,Si)-ordered natrolite, we can conclude that the order in tetrahedral
atoms does not affect the heat capacity. The analysis of derivatives dC/dT for natrolite, paranatrolite, and tetranatrolite has indicated that the water- cations subsystem within the highly hydrated
zeolite may become unstable at temperatures above 200 K.
Received: 30 July 2001 / Accepted: 15 November 2001 相似文献
10.
G. M. da Costa E. Van San E. De Grave R. E. Vandenberghe V. Barrón L. Datas 《Physics and Chemistry of Minerals》2002,29(2):122-131
A novel method for synthesis of aluminium hematites, based upon the homogeneous precipitation of Fe and Al oxinates in various proportions, is presented. The precursor precipitates are heated in air at 700?°C. X-ray diffraction, thermal analyses, BET, FTIR, optical reflection analysis, TEM and Mössbauer spectroscopy at room temperature and 80?K of the resulting products indicate that single-phase hematites are formed with structural Al substitution of up to 10 at%. Interestingly, the particle size (>100?nm) is not substantially reduced by the Al content. Although it remains difficult to obtain a homogeneously distributed Al substitution in the final hematite, this processing line offers a unique opportunity to separate the effects of grain size and Al substitution on the Morin transition temperature (T M) of Al hematite. From the comparison between the present hematites and a series of Al-substituted hematites with lepidocrocite as precursor, it could be shown that the effect on T M, associated with a change of a factor 10 in grain size, is about 1/3 of the effect caused by a change of 10 in the degree of substitution. Finally, it is suggested that proper thermal treatments under different conditions of the same precursors are likely to produce spinel phases. 相似文献