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排序方式: 共有89条查询结果,搜索用时 93 毫秒
1.
Determination of cadmium(II), copper(II), manganese(II) and nickel(II) species in Antarctic seawater with complexing resins 总被引:1,自引:0,他引:1
Raffaela Biesuz Giancarla Alberti Girolamo D'Agostino Emanuele Magi Maria Pesavento 《Marine Chemistry》2006,101(3-4):180-189
The strong species of cadmium(II), copper(II), manganese(II) and nickel(II) in an Antarctic seawater sample are investigated by a method based on the sorption of metal ions on complexing resins. The resins compete with the ligands present in the sample to combine with the metal ions. Two resins with different adsorbing strengths were used. Very stable metal complexes were investigated with the strong sorbent Chelex 100 and weaker species with the less strong resin, Amberlite CG-50. Strong species were detected for three of the considered metal ions, but not for Mn(II). Cu(II) is completely linked to species with a side reaction coefficient as high as log αM(I) = 11.6 at pH = 7.3. The ligand concentration was found to be similar to that of the metal ion, and the conditional stability constant was around 1020 M− 1. In the considered sample, only a fraction of the metal ions Cd(II) and Ni(II) is bound to the strong ligands, with side reaction coefficients equal to log αM(I) = 5.5 and 6.5 at pH = 7.3 for Cd(II) and Ni(II), respectively. These findings were confirmed by the test with the weaker sorbent Amberlite CG-50. It can be calculated from the sorption equilibria that neither Mn(II) nor Ni(II) is adsorbed on Amberlite CG-50 under the considered conditions and, in fact, only a negligible fraction of Mn(II) and Ni(II) was adsorbed. A noticeable fraction of Cd(II) was adsorbed on Amberlite CG-50, meaning that cadmium(II) is partially linked to weak ligands, possibly chloride, while no copper(II) was adsorbed on this resin, confirming that copper(II) is only combined in strong species. These results are similar, but not identical, to those obtained for other seawater samples examined in previous investigations. 相似文献
2.
Hiroshi Hasumoto Tsuneo Imazu Toshiaki Miura Kazuhiro Kogure 《Journal of Oceanography》2006,62(1):99-103
The use of an optical oxygen sensor to measure dissolved oxygen in seawater was investigated. The sensor is based on the dynamic
quenching of an oxygen-sensitive fluorochrome embedded in the tip. Dissolved oxygen in seawater samples collected from eight
stations at depths ranging from 3000 to 6000 m was analyzed both with the optical sensor and by the Winkler titration method.
The two sets of data did not differ significantly. The stability and simplicity of the method and the good agreement of the
results with those of the titration method indicate that the sensor would be useful for fieldwork. 相似文献
3.
将多元校正分析法应用于配位滴定中,以EDTA为滴定剂,玻璃电极为指示电极,饱和甘汞电极为参比电极。依据电位滴定原理,对混合三组分:Cu ̄(2+)、Cd ̄(2+)、Zn ̄(2+)、及Cu ̄(2+)、CO ̄(2+)、Ni ̄(2+)进行测定,各金属离子之间的△logK在0.04~2.34之间,计算误差一般小于土10%。 相似文献
4.
名铁矿中三氧化二铝含量测定的方法研究 总被引:1,自引:0,他引:1
名铁矿试样经碱熔,直接分离铁,再酸化,中和后用六次甲基四胺沉淀铝与络合物,沉淀酸溶,用氟盐取代-EDTA容量法测定三氧化二铝。该法充分消除了铁的干扰,使滴定终点比DZG93-012(铬铁矿操作规程-氟盐取代)-EDTA容量法测定三氧化二铝)方法的滴定终点更清晰,准确,结果重现性好。 相似文献
5.
氢醌滴定法测定金矿石中金的不确定度评定 总被引:5,自引:4,他引:5
以氢醌滴定法测定金矿石中贵金属金的实例进行不确定度评定。测量结果的不确定度由配制金标准母液、金标准工作液、氢醌滴定液浓度、称样质量、滴定样品所用氢醌溶液体积等所引入的不确定度分量组成。在对各个不确定度分量进行量化的基础上,通过合成得到测量结果的标准不确定度,再乘以95%置信概率下的扩展因子2,得到测量结果的扩展不确定度。 相似文献
6.
7.
自动电位滴定技术精确测定铜矿石中高含量铜的方法研究 总被引:2,自引:2,他引:0
铜矿石中百分含量铜的分析通常采用手动目视滴定法,该方法借助化学指示剂判定终点,存在终点判断和人为操作等误差,精密度、可靠性相对较差。基于此,本文建立了精确测定铜矿石中高含量铜的分析方法,采用智能型自动电位滴定仪自动判定终点,高分辨加液器精确控制硫代硫酸钠标准溶液加入量至0.001 m L,并且通过加大碘化钾用量使得滴定中产生的碘化亚铜被高浓度的I-溶解,消除对碘的吸附影响。本法应用于铜含量为24.2%~59.09%的铜精矿、黄铜矿、铅黄铜国家标准物质分析,相对标准偏差(RSD,n=10)0.3%,极差仅为0.13%、0.21%、0.29%,优于手动目视滴定法。本法提高了铜矿石分析的自动化程度,适用于精确测定铜含量大于0.5%尤其是10%以上的铜矿石。 相似文献
8.
The model selection from EMF data of pH titration curves has been studied for binary and ternarysystems(Ni~(2+)-glycine and Ni~(2+)-methionine-taurine respectively)by using the MINIGLASSprogram.Comparison between experimental and calculated titration curves with this interactive programindicates the presence(and the pH range)of the different species in equilibrium. 相似文献
9.
The Cercis siliquastrum tree leaves are introduced as a low cost biosorbent for removal of Ag(I) from aqueous solution in a batch system. FT‐IR, XRD analysis, and potentiometric titration illustrate that the adsorption took place and the acidic functional group (carboxyl) of the sorbent was involved in the biosorption process. In addition, it was observed that the pH beyond pHpzc 4.4 is favorable for the removal procedure. The effect of operating variables such as initial pH, temperature, initial metal ion concentration, and sorbent mass on the Ag(I) biosorption was analyzed using response surface methodology (RSM). The proposed quadratic model resulting from the central composite design approach (CCD) fitted very well to the experimental data. The optimum condition obtained with RSM was an initial concentration of Ag(I) of 85 mg L?1, pH = 6.3 and sorbent mass 0.19 g. The applicability of different kinetic and isotherm models for current biosorption process was evaluated. The isotherm, kinetic, and thermodynamic studies showed the details of sorbate‐sorbent behavior. The competitive effect of alkaline and alkaline earth metal ions during the loading of Ag(I) was also considered. 相似文献
10.