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91.
Lead-arsenic soil geochemical study as an exploration guide over the Killik volcanogenic massive sulfide deposit, Northeastern Turkey 总被引:3,自引:0,他引:3
A mountainous terrain, the eastern Pontide tectonic belt, located in northeastern Turkey, contains more than 60 known volcanogenic massive sulfide (VMS) deposits that differ in reserves (0.1–30 million tonnes) and grades. Soil geochemistry is conventionally used in exploration programs to discover concealed VMS deposits in the region. In the present study, Pb and As element pair were used as pathfinder elements to investigate the relationship of their anomalies to a completely delineated ore deposit (Killik VMS deposit) in an orientation survey that served as a natural physical model. Two hundred forty soil samples were analyzed in the present study. The two elements, which represent the opposite ends of the mobility range, revealed high contrast and overlapped each other at the location of the ore deposit due to enhancement of the anomalies by hydromorphic dispersion, which is an indication that soil samples would produce reliable results. The successful delineation of the deposit is remarkable considering the rough topography and the climatic limitations. Previously the extremely moist and temperate climate was thought to cause excessive leaching of the trace element pathfinders from the ore deposits to produce extensive anomalies usually extending away from the mineralization thus, leading to erroneous results and/or extensive anomalous areas. But the present research has shown that the method can be used effectively if the sampling and data evaluation is carefully conducted. 相似文献
92.
Improved Platinum-Group Element Extraction by NiS Fire Assay from Chromitite Ore Samples Using a Flux Containing Sodium Metaphosphate 总被引:1,自引:0,他引:1
Many chromite-rich rocks contain relatively high concentrations of the platinum-group elements (PGE). In many cases, the phases carrying PGE occur as either platinum-group minerals (PGM) or as base metal sulfides in solid solution in sulfides. In some cases, such as the UG-2 unit of the Bushveld Complex, the PGM are occluded inside chromite grains. Chromites are notably difficult to dissolve in most fluxes and if the chromite contains some PGM the possibility exists that not all the PGE will be recovered during fusion. In this work, shortcomings in published methods of analysis based on the nickel sulfide fire assay procedure were investigated and a new procedure developed based on the addition of sodium metaphosphate to the fusion mixture. Optimum composition of the fusion mixture was found to be 10 g sodium metaphosphate and 9 g silica to 10 g sample, 15 g sodium carbonate, 30 g lithium tetraborate, 7.5 g nickel and 4.5 g sulfur to achieve complete dissolution of chromite grains. The new flux mixture was evaluated by the analysis of reference material CHR-Pt+ (which is known to contain PGM inside chromite grains) and no undissolved chromite grains were found in the glassy slag. Analysis of the nickel sulfide beads from this fire assay using neutron activation analysis showed similar results for Rh and Ru when compared with published conventional true (or accepted) values, while Au, Ir, Os, Pd and Pt values determined here were 10 to 30% higher than the corresponding published conventional true values. It was concluded that the addition of sodium metaphosphate improved chromite dissolution in the flux and appears to improve PGE recovery. 相似文献
93.
Abstract. The Takara volcanogenic massive sulfide (VMS) deposit occurs in Miocene formation of the Misaka Mountain, the South Fossa Magna region, central Japan. The tectonic setting of the Misaka Mountain is reconstructed to be a part of the paleo Izu-Ogasawara arc which collided with the Honshu arc and to form accreted body in the present position. The Takara deposit, therefore, is considered to have formed in the paleo Izu-Ogasawara arc.
The ores from the Takara deposit are classified into pyrite-type ore, chalcopyrite-type ore, and sphalerite-type ore on the basis of chemical composition and their mineral assemblages. Some pyrite-type ores are characterized by their high Au content. The Au content is hardly recognized in the chalcopyrite-type and sphalerite-type ores.
The ores from the Takara deposit have intermediate bulk chemical composition between those from the Besshi-type deposits and the Kuroko-type deposits that are two representative VMS deposits. However, the bulk chemical composition is closer to that from the Kuroko-type deposits. And moreover, chemical composition of tetrahedrite-tennantite series minerals (tetrahedrite) is similar to that from the Kuroko-type deposits. The bulk chemical composition (Cu, Zn, Co, Pb, and As contents) of ores is affected by the chemical composition of volcanic rocks associated with VMS deposits. 相似文献
The ores from the Takara deposit are classified into pyrite-type ore, chalcopyrite-type ore, and sphalerite-type ore on the basis of chemical composition and their mineral assemblages. Some pyrite-type ores are characterized by their high Au content. The Au content is hardly recognized in the chalcopyrite-type and sphalerite-type ores.
The ores from the Takara deposit have intermediate bulk chemical composition between those from the Besshi-type deposits and the Kuroko-type deposits that are two representative VMS deposits. However, the bulk chemical composition is closer to that from the Kuroko-type deposits. And moreover, chemical composition of tetrahedrite-tennantite series minerals (tetrahedrite) is similar to that from the Kuroko-type deposits. The bulk chemical composition (Cu, Zn, Co, Pb, and As contents) of ores is affected by the chemical composition of volcanic rocks associated with VMS deposits. 相似文献
94.
内蒙古镁铁质-超镁铁质岩型铜镍矿床成矿条件与找矿远景分析 总被引:5,自引:2,他引:5
按构造环境控岩控矿特点,划分区内铜镍型矿成矿(岩)带,分析成矿条件,研究了与该类矿床成矿有关的镁铁质岩、超镁铁质岩分布规律及铜镍硫化物成矿特征,提出了找矿方向和建议. 相似文献
95.
96.
A Study of DMS Oxidation in the Tropics: Comparison of Christmas Island Field Observations of DMS, SO2, and DMSO with Model Simulations 总被引:2,自引:0,他引:2
G. Chen D. D. Davis P. Kasibhatla A. R. Bandy D. C. Thornton B. J. Huebert A. D. Clarke B. W. Blomquist 《Journal of Atmospheric Chemistry》2000,37(2):137-160
This study reports comparisonsbetween model simulations, based on current sulfurmechanisms, with the DMS, SO2 and DMSOobservational data reported by Bandy et al.(1996) in their 1994 Christmas Island field study. For both DMS and SO2, the model results werefound to be in excellent agreement with theobservations when the observations were filtered so asto establish a common meteorological environment. Thisfiltered DMS and SO2 data encompassedapproximately half of the total sampled days. Basedon these composite profiles, it was shown thatoxidation of DMS via OH was the dominant pathway withno more than 5 to 15% proceeding through Cl atoms andless than 3% through NO3. This analysis wasbased on an estimated DMS sea-to-air flux of 3.4 ×109 molecs cm-2 s-1. The dominant sourceof BL SO2 was oxidation of DMS, the overallconversion efficiency being evaluated at 0.65 ± 0.15. The major loss of SO2 was deposition to theocean's surface and scavenging by aerosol. Theresulting combined first order k value was estimated at 1.6 × 10-5 s-1. In contrast to the DMSand SO2 simulations, the model under-predictedthe observed DMSO levels by nearly a factor of 50. Although DMSO instrument measurement problems can notbe totally ruled out, the possibility of DMSO sourcesother than gas phase oxidation of DMS must beseriously considered and should be explored in futurestudies. 相似文献
97.
铜镍硫化物矿床的成冈——以诺里尔斯克(俄罗斯)和金川(中国)为例 总被引:15,自引:0,他引:15
与超基性岩浆作用有关的铜镍硫化物矿床主要有两种成矿建造,一种为含铬建造,另一种为含铂建造。尖晶石类矿物成分的变化清楚地反映了这两类建造的成矿属性,含铬建造的尖晶石属于铬铁矿-尖晶石系列,含铂建造中则为尖晶石-磁铁矿系列。从含铬建造向含铂建造转变的原因,可以解释为超基性岩艇中硫的作用增加,从而引起反应:4FeO+S=FeS+Fe3O4(磁铁矿),同时分散性铂族元素的专属性特征也发生相应变化(Ru+Os+Ir)→(Pt+Pd)。因此,含铬建造中主要富含Ru、Os和Ir,而含铂建造中则富含Pt和Pd。超基性岩浆作用中硫的化学活动性增加与基碱度增加直接有关。因此,含铂的超基性岩大多数情况下与富碱的玄武岩形成共生组合,当富铁熔浆发生硫化作用时,将会导致硫化物与硅酸岩熔浆的不混融,从而形成矿浆,据此,金川含铂铜镍矿石不是矿 相似文献
98.
Microstructural tectonometamorphic processes and the development of gneissic layering: a mechanism for metamorphic segregation 总被引:6,自引:1,他引:5
The Mary granite, in the East Athabasca mylonite triangle, northern Saskatchewan, provides an example and a model for the development of non-migmatitic gneissic texture. Gneissic compositional layering developed through the simultaneous evolution of three microdomains corresponding to original plagioclase, orthopyroxene and matrix in the igneous rocks. Plagioclase phenocrysts were progressively deformed and recrystallized, first into core and mantle structures, and ultimately into plagioclase-rich layers or ribbons. Garnet preferentially developed in the outer portions of recrystallized mantles, and, with further deformation, produced garnet-rich sub-layers within the plagioclase-rich gneissic domains. Orthopyroxene was replaced by clinopyroxene and garnet (and hornblende if sufficient water was present), which were, in turn, drawn into layers with new garnet growth along the boundaries. The igneous matrix evolved through a number of transient fabric stages involving S-C fabrics, S-C-C' fabrics, and ultramylonitic domains. In addition, quartz veins were emplaced and subsequently deformed into quartz-rich gneissic layers. Moderate to highly strained samples display extreme mineralogical (compositional) segregation, yet most domains can be directly related to the original igneous precursors. The Mary granite was emplaced at approximately 900 °C and 1.0 GPa and was metamorphosed at approximately 750 °C and 1.0 GPa. The igneous rocks crystallized in the medium-pressure granulite field (Opx–Pl) but were metamorphosed on cooling into the high-pressure (Grt–Cpx–Pl) granulite field. The compositional segregation resulted from a dynamic, mutually reinforcing interaction between deformation, metamorphic and igneous processes in the deep crust. The production of gneissic texture by processes such as these may be the inevitable result of isobaric cooling of igneous rocks within a tectonically active deep crust. 相似文献
99.
100.