全文获取类型
收费全文 | 98篇 |
免费 | 16篇 |
国内免费 | 35篇 |
专业分类
测绘学 | 6篇 |
大气科学 | 1篇 |
地球物理 | 19篇 |
地质学 | 104篇 |
海洋学 | 7篇 |
综合类 | 5篇 |
自然地理 | 7篇 |
出版年
2024年 | 1篇 |
2023年 | 2篇 |
2022年 | 3篇 |
2020年 | 2篇 |
2019年 | 3篇 |
2018年 | 2篇 |
2017年 | 1篇 |
2016年 | 3篇 |
2015年 | 5篇 |
2014年 | 6篇 |
2013年 | 8篇 |
2012年 | 2篇 |
2011年 | 12篇 |
2010年 | 5篇 |
2009年 | 7篇 |
2008年 | 3篇 |
2007年 | 2篇 |
2006年 | 6篇 |
2005年 | 8篇 |
2004年 | 6篇 |
2003年 | 6篇 |
2002年 | 4篇 |
2001年 | 11篇 |
2000年 | 9篇 |
1999年 | 2篇 |
1998年 | 7篇 |
1997年 | 3篇 |
1996年 | 5篇 |
1995年 | 1篇 |
1994年 | 1篇 |
1993年 | 6篇 |
1992年 | 2篇 |
1991年 | 1篇 |
1990年 | 2篇 |
1989年 | 1篇 |
1985年 | 1篇 |
排序方式: 共有149条查询结果,搜索用时 31 毫秒
51.
Secondary reactions occurring in pyrite-containing sediments from open cut coal mines are complex and not fully understood. In this study, the changes in seepage water composition in a column experiment with a sediment containing pyrite (5.6 g kg−1) were evaluated using a chemical equilibrium model. A column experiment with artificial irrigation (730 mm water yr−1) was carried out for 2 yr with a sediment from the open pit mine Garzweiler, Germany, at the Institute of Applied Geology. Tracer (LiCl) was added to the sediment. Seepage water composition at 52 cm depth was sampled weekly. Redox potential and the water potential were also recorded weekly. Sulphate and Fe(II) were the dominant ions in the seepage water with concentration maxima of 500 and 350 mmol l−1 after 50 days (0.7 pore volumes (PV)). Minimum pH values were around 0.8 after 100 days (1.4 PV), but increased subsequently and reached 2.4 after 700 days (9.5 PV). Ion activity product calculations indicated the intermediate formation of gypsum (19th–480th day of the experiment). Solutions were undersaturated with respect to alunite, jarosite, jurbanite, schwertmannite, melanterite, gibbsite and goethite during the whole experiment. The model of coupled equilibria which included inorganic complexation, precipitation/dissolution of gypsum and multiple cation exchange was tested. Pyrite oxidation and pH-dependent silicate weathering were considered using simple input functions. Transport was modelled using a field capacity cascade submodel. Model results showed satisfactory agreement with measured values for pH and concentrations of SO4, Fe, Mg, Ca and Al. Correlation coefficients lay between 0.7 and 0.9 and linear regression coefficients (modelled against measured) were 1.5 (Ca), 1.0 (Fe, SO4), 0.8 (Mg), 0.7 (pH) and 0.6 (Al). The results showed that the protons produced during pyrite oxidation (94 mmolc H+ kg−1) were mainly released into seepage water (as HSO4− and H+). Cation exchange reactions buffered 20 mmolc of H+ kg−1 sediment, and Al released by silicate weathering accounted for 3.6 mmolc H+ kg−1. Modelling was useful to further understand the significance of different pH buffer reactions. 相似文献
52.
53.
采用氯化铵交换-原子吸收光谱法和CaCl2-甲醛缩合法测定3个金云母-蛭石间层矿物样品的各阳离子交换分量和阳离子交换总量,通过分析样品粒度和溶液pH值对阳离子交换容量的影响及晶层端面水解使表面荷电的特点,确定样品的等电点.结果表明,随着粒度的增大,样品的阳离子交换容量逐渐减小;随着pH值的增大,样品的阳离子交换容量先急剧减小(pH=2~5),后趋于平缓(pH=5~9),而后再急剧减小(pH=9~11.5),这些变化主要与晶层端面的水解作用和八面体片阳离子的溶出作用有关;样品的等电点为pH值≈9.研究结果对于排除端面水解作用对阳离子交换容量的影响和进一步确定蛭石晶层的层电荷具有重要的意义. 相似文献
54.
S.Ismael H.M.Baioumy 《中国地球化学学报》2003,22(4):337-344
Classic physical and chemical treatments applied to separating clay minerals from the host sediments are often difficult or aggressive for clay minerals. A technique using cation exchange resins (amberlite IRC-50H and amberlite IR-120) is used to separate clay minerals from the host sediments. The technique is based on the exchange of cations in the minerals that may be associated clay minerals in sediments, such as Ca and Mg from dolomite; Ca from calcite, gypsum and francolite with cations carried by resin radicals. The associated minerals such as gypsum, calcite, dolomite and francolite are removed in descending order. Separation of clay minerals using cation exchange resins is less aggressive than that by other classic treatments. The efficiency of amberlite IRC-50H in the removal of associated minerals is greater than that of amberlite IR-120. 相似文献
55.
利用天然矿物蛭石的阳离子交换特点,通过离子交换法将Cu^2 植入到蛭石中,制得铜含量高达5.5%(相当于蛭石阳离子交换容量的80%)、具良好抗菌性能的铜型蛭石。经XRD、TEM、AAS分析,结合晶胞参数及晶体化学式的计算,铜型蛭石的XRD特征值更接近于标准的Mg^-蛭石,这与Cu^2 与Mg^2 半径相近,电价相等的特点相符合,Cu^2 部分以水合物的形式存在于蛭石层间,部分进入八面体中以六次配位的形式存在。铜型蛭石的a0和b0值无明显变化而c0值略有减小,这对于Cu^2 的稳定是有利的,上述各特点有利于铜型蛭石抗菌剂的稳定性和持久性。 相似文献
56.
57.
阴离子交换树脂已被应用于酸法消解-电感耦合等离子体质谱(ICP-MS)测定铜铅锌矿石等地质样品中铼的分离富集,样品溶液中的ReO_4~-用树脂交换吸附后再用洗脱剂将ReO_4~-选择性洗脱,该方法流程长,影响其稳定性和准确性。本文以基体元素为吸附交换目标,用8 g的732强酸型阳离子交换树脂在2%硝酸介质条件下静态吸附1.5 h,可有效地消除基体元素的影响。用空矿(石英)稀释低含量铼的样品做空白试验,获得方法检出限为0.004μg/g,精密度(RSD)小于6%,加标回收率为96%~104%。本方法应用的732强酸型阳离子交换树脂在适宜酸度条件下,对矿石中除钨、钼以外的金属元素吸附率高达95%以上,降低了样品溶液离子强度和干扰元素浓度,实现了ICP-MS的直接测定,操作方法比阴离子交换吸附法简便。 相似文献
58.
Effects of cation substitutions in garnet and pyroxene on equilibrium oxygen isotope fractionations 总被引:3,自引:0,他引:3
High-grade metamorphic rocks were used to explore oxygen isotope fractionations between pyroxene and garnet, and to investigate the effects on fractionation factors of the cation substitutions Fe3+Al?1 and Ca(Fe,Mg)?1. Recrystallized, granulite facies (725 °C) wollastonite ores from the northern Adirondack highlands contain essentially only the minerals clinopyroxene (a Di–Hd solid solution)+garnet (a Grs–Adr solid solution)±wollastonite, and exhibit a systematic dependence of measured fractionations on the Fe3+ content of calcic garnet: Δ(Cpx–CaGrt)=(0.14±0.12)+(0.78±0.20)XAdr and Δ(Wo–CaGrt)=(0.15±0.22)+(0.57±0.33)XAdr. In eclogites formed at T ≤650 °C, measured compositions of Ca-poor garnet and omphacite combined with experimental data indicate that Ca-poor, Fe-rich garnet is enriched in 18O compared to both diopside and grossular: extrapolating to 1000 K, Δ(Alm–Di)≈c. 0.2 and Δ(Alm–Grs)≈c. 0.5. Orthopyroxene and clinopyroxene from Gore Mountain, New York, show a constant fractionation that is independent of rock type, as expected if they have the same closure temperature. These data imply Δ(Opx-Cpx)≈c. 0.7 at 1000 K. Measured fractionations among Ca-poor garnet, orthopyroxene, clinopyroxene and hornblende in the Gore Mountain rocks further indicate an 18O enrichment in Ca-poor garnet over Grs (≈c. 0.5 at 1000 K). The new measurements are indistinguishable from expected equilibrium values based on experiments for the minerals enstatite, diopside, grossular, wollastonite and feldspar, but consistently indicate a significant isotope effect for the simple octahedral cation substitutions Fe3+Al?1 (Grs vs. Adr) and Ca(Fe,Mg)?1 (Ca-poor garnet vs. Grs; Opx vs. Cpx). Neither cation substitution has been directly investigated for its effect on 18O/16O fractionation with experiments in silicates. Chemical characterization of minerals is required prior to petrological interpretation of oxygen isotope trends. 相似文献
59.
氮迁移转化对地下水硬度升高的影响 总被引:15,自引:0,他引:15
城市地下水硬度升高是一个普遍的环境问题,研究表明地下水硬度高值区与硝酸盐污染在空间上的分布具有一致性。通过室内土柱试验和化学热力学模拟,讨论了污水入渗过程中氮迁移转化对水土系统钙镁迁移的影响。结果表明:在连续入渗条件下,阳离子交换作用是控制地下水硬度升高的主要过程;在间歇入渗条件下,硝化作用改变了土水系统的酸碱条件,使钙镁难溶盐溶解,导致地下水硬度升高。 相似文献
60.
基于岩浆铬矿床与超镁铁质岩石的关系,从元素亲合性和共生规律的角度揭示了铝对铬成矿制约的主导作用。分析了铝和铬亲石、亲氧的二重性及其晶体化学的依存关系。论证了超镁铁Si-O体系中铝丰度过高或过低均不利于铬的成矿。揭示了制约因素分散富集的因素都是在一定条件下互为依存和转化的。是在动态中的矛盾的对立和统一。 相似文献