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101.
102.
Synthetic titanite, CaTiOSiO4, and the series of (Ca1−x
Na
x
)(Ti1−x
Ta
x
)OSiO4 and Ca(Ti1−2x
Ta
x
Al
x
)OSiO4 solid solutions have been prepared by ceramic methods, and their crystal structure determined by the Rietveld analysis. At ambient conditions, titanite can contain up to 20 mol% NaTaOSiO4 or 60 mol% Ca(Al0.5Ta0.5)OSiO4. These limits might differ in natural samples due to combination with substitutions involving fluorine and/or hydroxyl replacing oxygen together with vacancies at cationic sites. All cations located at the vii
X- and vi
Y-sites in the structures of tantalian titanite are disordered. Expansion of the <Si–O> bond from 1.618 to 1.621 Å in CaTi0.8Ta0.1Al0.1OSiO4 and CaTi0.6Ta0.2Al0.2OSiO4 to 1.644 Å in the CaTi0.4Ta0.3Al0.3OSiO4 titanite suggests the possible presence of some Al3+ in the tetrahedral site replacing Si4+ in the latter. All tantalian titanites crystallize in the space group A2/a. This implies that both single-site and complex double-site substitutional schemes induce P21/a → A2/a phase transition(s). The (Ca1−x
Na
x
)(Ti1−x
Ta
x
)OSiO4 substitution scheme incorporates larger cations at both the vii
X and vi
Y sites, whereas the Ca(Ti1−2x
Ta
x
Al
x
)OSiO4 scheme involves only vi
Y-site (Al3+,Ta5+) cations with a slightly smaller “average” radius. Unit cell dimensions change insignificantly or increase incrementally with increase of average cationic radii in the (Ca1−x
Na
x
)(Ti1−x
Ta
x
)OSiO4 series, and with an insignificant decrease in the viR
Y
average cationic radii in the Ca(Ti1−2x
Ta
x
Al
x
)OSiO4 series. Both Ta-doped titanite and CaTiOSiO4 consist of distorted polyhedra with the XO7, YO6 coordination polyhedra and the SiO4 tetrahedron in tantalian titanite being less distorted compared to those of the pure CaTiOSiO4. 相似文献
103.
104.
正It is well known that boron exists as polyborate anions in aqueous solution.Boron atom can coordinates to three or four oxygen atoms and borate can exist as not only the monomer but also the polymer.The polymerization 相似文献
105.
湖南七里坪-半边街接触交代型硼矿,矿体产于中石炭统壶天群白云岩与燕山期花岗岩接触带的矽卡岩中,产状受岩体顶板形态的控制,多为似层状、透镜状、囊状等。一般离岩体较远的部位硼矿石的品位较富,但靠近岩体的部位矿体较厚大。据微量元素相关系数聚类谱系图分析,B元素在岩体中呈分散状态,在高温热液中易于聚集,在矽卡岩中富集成矿,在蚀变的白云岩中有轻微的富集。 相似文献
106.
在对宽甸砖庙硼矿床的研究中发现了电气石与遂安石共生的现象,电气石为钙镁电气石,由电子探针分析结果计算的晶体化学式为:(Ca0.59Na0.355K0.06)(Mg2.557Fe0.1512+Ti0.013Cr0.002Ni0.006)(Al5.416Fe0.5642-(BO3)3Si 6.16 O16(OH)4,同围岩中的电气石相比:(1)淡绿色,多色性弱;(2)折射率为Ne=1.646,Ns=1.624;(3)成分上富Mg(MgO 11.47%)和Ca(CaO3.14%);相对贫Na(Na2O 1.09%),Fe(FeO4.63%)和Al(Al2O326.69%)(4)结构上d101=3.393A,a0=15.957±0.002,c0=7.227±0.001;(5)红外光谱晶格Si-O4四面体振动I1001>I1036。这些标型特征具有硼矿床的找矿指示意义。 相似文献
107.
Comparison of Fused Glass Beads and Pressed Powder Pellets for the Quantitative Measurement of Al,Fe, Si and Ti in Bauxite by Laser‐Induced Breakdown Spectroscopy
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Alexandrina A. C. Carvalho Victoria C. Alves Daniel M. Silvestre Flávio O. Leme Pedro V. Oliveira Cassiana S. Nomura 《Geostandards and Geoanalytical Research》2017,41(4):585-592
Due to matrix interference and sample particle size effects, some of the most important and difficult issues in laser‐induced breakdown spectroscopy (LIBS) analysis are the calibration and quantitative measurement of a complex matrix. This study proposes the use of borate fusion as an alternative sample preparation procedure for the quantitative measurement of Al, Fe, Si and Ti in bauxite by LIBS. Analytical calibration curves were made using bauxite certified reference materials (CRM), and the precision and accuracy of the methods were evaluated by analysing an additional bauxite CRM, using two different approaches: pressed powder pellets and fused glass beads. The borate fusion method was the most suitable sample preparation technique, since particle size effects and matrix interference could be minimised, obtaining better linearity on the analytical calibration curves (r2), and more accurate and more precise results for bauxite analysis. 相似文献
108.
辽东-吉南地区早元古代硼镁石型硼矿床地质特征及矿床成因 总被引:1,自引:0,他引:1
通过对辽东-吉南硼矿床地质特征、矿床地球化学及O、C、B同位素特征的研究,结合数学地质方法分析认为辽东-吉南地区早元古代硼矿的成矿作用可分为沉积成岩成矿和变质-混合岩化改造成矿这两个主要成矿期。矿床成因类型为沉积变质改造型 相似文献