热液体系氢、氧同位素分馏机制及其地质意义   总被引：9，自引：0，他引：9  

陈振胜  张理刚 《地质学报》1992,66(2):158-169

探讨了热液体系氢、氧同位素地球化学行为及其与水/岩交换同位素分馏的内在关系。有效W/R值是除温度条件外,另一控制蚀变岩石和热液水氢、氧同位素组成变化的因素。此外还根据数个矿区成矿热液水和蚀变岩石氢、氧同位素组成及变化特征对水/岩交换和W/R值的应用及地质意义展开讨论。最后提出热液体系中大气降水和岩浆热液水氢、氧同位素组成演化模式简图。  相似文献   

Studies on Separation of Heavy Metals from Acidic Solutions by Foam Fractionation with Respect to an Application on Acidic Soil Extracts     

S. Wmmel  W. Calmano 《洁净——土壤、空气、水》1992,20(5):265-268

An experimental investigation is presented on the batch foam fractionation of the heavy metal cations Pb²⁺, Cd²⁺, Cu²⁺, Sb³⁺ and As⁵⁺ from diluted aqueous solutions with hexamethylenedithiocarbamate (HMDC) as complexing agent and sodiumdodecylsulfate (SDS) as surfactant. Among the considered pH-values of 2,4 and 7 the pH 2 experiments allow a direct application of foam fractionation on acidic extracts from heavy metal contaminated soil. The experiments at pH 2 and pH 4 show better results than those at neutral pH. Although a simple device was used, a maximum enrichment factor of 13.8 and a minimum removal factor of 0.01 have been measured. The flotation with weak organic acids like citric acid (CA) and acetic acid (AA) show about 50–70% smaller enrichment factors than those acidified with hydrochloric acid. The dissolution and mixing of the reacting components as well as the concentration of the detergent and the gaseous volume flow can be regarded as basic parameters of foam fractionation.  相似文献   

稳定氯同位素分馏机理及其应用的研究     

王佩仪 《地质科技情报》1993,12(3):83-88

过去一直认为稳定氯同位素比值(~(37)Cl/~(35)Cl)几乎不变。80年代以来利用高精度质谱法成功地发现了自然界氯同位素分馏作用。单纯的溶解和对流迁移作用不能引起同位素组分变化,而扩散作用、离子渗透作用和对流混合作用却可导致同位素分馏。各地不同深度海水的氯同位素成分极为一致,故以标准平均海水氯(SMOC)作为对比标准。得克萨斯—路易斯安那海湾油田水的δ~(37)Cl大致为+0.5‰~-1.25‰,且与氯浓度大致呈正相关。热液成矿系统中,氯同位素可作为研究矿床成因的示踪剂,如美国田纳西州密西西比河谷型矿床(MVD)的δ~(37)Cl在+0.2‰~-1.1‰之间,几个斑岩铜矿床(PVD)的早期脉岩与晚期脉岩中不同δ~(37)Cl的存在,都表明在成矿过程中有不同氯源的参与。  相似文献   

Intracrystalline fractionation of Fe in synthetic (Fe, Mg, Zn) - bearing staurolite: a Mössbauer spectroscopic study     

M. Koch-Müller  I. Abs-Wurmbach  W. Bubenik 《Physics and Chemistry of Minerals》1999,26(4):312-321

⁵⁷Fe-Mössbauer spectra of eleven Fe-Mg-bearing staurolite samples, synthesized at 5, 20 and 25 kbar and 680°C, ranging in composition from x_Fe?=1.00 to x_Fe?=0.15, and of two Zn-Fe-bearing staurolite samples, synthesized at 20 kbar and 700°C with x_Fe?=0.10 and x_Fe?=0.32 were collected at room temperature. The spectra reveal that about 80% of Fe_tot (in case of Fe-Mg-bearing staurolite) and about 70% of Fe_tot (in case of Fe-Zn-bearing staurolite) are located as Fe²⁺ at the three subsites Fe1, Fe2 and Fe3 of the tetrahedral T2-site. The refinement of the spectra results in almost identical values for the isomer shift (IS) (±1.0 mm/s) but significantly different values for the quadropole splitting (QS) for the three subsites which is in accordance with the different distortions of these sites. About 8% of Fe_tot (in case of Fe-Mg-bearing staurolite) and 13% of Fe_tot (in case of Fe-Zn-bearing staurolite) are located as Fe²⁺ at the octahedral M4 site, while the remainder percents of Fe_tot indistinguishably occur as Fe²⁺ at the octahedral M1 and M2 sites of the kyanite-like part of the structure. Within the whole Fe-Mg-staurolite solid solution series the Mössbauer parameters QS of the sites M4 and (M1, M2) vary systematically with composition whereas IS remains constant. There is a high negative correlation of the total Mg-content with Fe-occupation of all the Fe-bearing sites indicating a continuous substitution of Fe²⁺ by Mg on all these sites. Synthetic Fe-staurolites show no increasing occupation of the octahedral sites by two-valent cations with pressure, as was assumed by several authors.  相似文献   

The role of coarse colloids as a carrier phase for trace metals in riverine systems   总被引：2，自引：0，他引：2  

Davide Vignati  Janusz Dominik 《Aquatic Sciences - Research Across Boundaries》2003,65(2):129-142

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Distribution and fractionation mechanism of stable carbon isotope of coalbed methane   总被引：1，自引：0，他引：1  

QIN Shengfei  TANG Xiuyi  SONG Yan  WANG Hongyan 《中国科学D辑(英文版)》2006,49(12):1252-1258

The stable carbon isotope values of coalbed methane range widely, and also are gener- ally lighter than that of gases in normal coal-formed gas fields with similar coal rank. There exists strong carbon isotope fractionation in coalbed methane and it makes the carbon isotope value lighter. The correlation between the carbon isotope value and Ro in coalbed methane is less obvious. The coaly source rock maturity cannot be judged by coalbed methane carbon isotope value. The carbon isotopes of coalbed methane become lighter in much different degree due to the hydrodynamics. The stronger the hydrodynamics is, the lighter the CBM carbon isotopic value becomes. Many previous investigations indicated that the desorption-diffusion effects make the carbon isotope value of coalbed methane lighter. However, the explanation has encountered many problems. The authors of this arti- cle suggest that the flowing groundwater dissolution to free methane in coal seams and the free methane exchange with absorbed one is the carbon isotope fractionation mechanism in coalbed methane. The flowing groundwater in coal can easily take more 13CH4 away from free gas and com- paratively leave more 12CH4. This will make 12CH4 density in free gas comparatively higher than that in absorbed gas. The remaining 12CH4 in free gas then exchanges with the adsorbed methane in coal matrix. Some absorbed 13CH4 can be replaced and become free gas. Some free 12CH4 can be ab- sorbed again into coal matrix and become absorbed gas. Part of the newly replaced 13CH4 in free gas will also be taken away by water, leaving preferentially more 12CH4. The remaining 12CH4 in free gas will exchange again with adsorbed methane in the coal matrix. These processes occur all the time. Through accumulative effect, the 12CH4 will be greatly concentrated in coal. Thus, the stable carbon isotope of coalbed methane becomes dramatically lighter. Through simulation experiment on wa- ter-dissolved methane, it had been proved that the flowing water could fractionate the carbon isotope of methane, and easily take heavy carbon isotope away through dissolution.  相似文献   

Lithium isotope fractionation in the southern Cascadia subduction zone   总被引：2，自引：0，他引：2  

Tom&#x; Magna  Uwe Wiechert  Timothy L. Grove  Alex N. Halliday 《Earth and Planetary Science Letters》2006,250(3-4):428-443

We present lithium (Li) abundances and isotope compositions for a suite of anhydrous olivine tholeiites (HAOTs) and hydrous basalt-andesitic (BA) lavas from the Mt. Shasta and Medicine Lake regions, California. The values of δ⁷Li vary from + 0.9‰ to + 6.4‰ and correlate inversely with distance from the trench. These data are consistent with continuous isotope fractionation of Li during dehydration of the subducted oceanic lithosphere, an interpretation corroborated by uniformly high pre-eruptive H₂O contents in basaltic andesites accompanied by high Li, Rb, Sr, Ba and Pb abundances. The subduction-derived component that was added to these hydrous magmas is shown to be very similar beneath both Mt. Shasta and Medicine Lake volcanoes despite characteristically distinct Li isotope compositions in the magmas themselves. More evolved andesites and dacites from Mt. Shasta have δ⁷Li from + 2.8 to + 6.9‰ which is identical with the range obtained for HAOTs and BA lavas from Mt. Shasta. Therefore, Li isotopes do not provide evidence for any other crustal component admixed to Mt. Shasta andesites or dacites during magmatic differentiation and magma mixing in the crust.  相似文献   

Element diffusion ability in metasomatic agents and its effect on chemical characteristics of metasomatized peridotites     

Y S O’Reilly 《中国科学D辑(英文版)》2006,49(9):926-937

The partial melting and metasomatism are two most important geological processes of changing chemical compositions of mantle. Extracting partial melt from primitive mantle leads residual mantle to deplete in- compatible elements, whereas the metasomatism …  相似文献   

多接收器等离子体质谱(MC-ICPMS)高精度测定Nd同位素方法   总被引：19，自引：1，他引：19  

何学贤  唐索寒  朱祥坤  王进辉 《地球学报》2007,28(4):405-410

多接收器等离子体质谱是近年发展起来的高精度同位素分析手段之一,通过用等离子体质谱测量Nd国际标准材料La Jolla和JMC Nd203以及实际样品GBW04419,研究MC-ICPMS测量Nd的质量分馏特点,解决MC-ICPMS测量的关键所在质量分馏校正.通过修正分馏系数,可以实现理想的分馏校正.结果显示出所得到的分析精度达到热电离质谱的测量水平.具有实际地质样品代表性的实验室内部标准CAGS-Nd-1重现性长期分析结果为:143Nd/144Nd=0.512072±0.000008(2σ,n=140).  相似文献   

对稳定同位素地球化学一个基本原理的反思     

刘耘 《矿物岩石地球化学通报》2007,26(1):49-51

用基于Urey模型的量子化学从头计算,揭示Fe在FeCN63-和FeCN46-中的不同“自旋态”对同位素分馏行为的巨大影响,说明了只考虑“价态”的做法是不正确的,修正了关于“重同位素倾向于富集在高价化合物中”的这个广泛被接受的基本原理。并首次指出在压力导致自旋态变化的地质过程中,必定存在同位素分馏反常的复杂状况,是值得进一步研究的方向。  相似文献