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首页> 外文期刊>Geochemistry International >Differential behavior of components of the 238U-206Pb and 235U-207Pb isotopic systems in polymineralic U ores
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Differential behavior of components of the 238U-206Pb and 235U-207Pb isotopic systems in polymineralic U ores

机译:多矿物矿石中238U-206Pb和235U-207Pb同位素系统的组分的差异行为

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U-Pb systems were examined in samples (ranging from 4 to 10 cm3 in volume) of ore material taken from along a 3.5-m profile across a zone of U mineralization exposed in an underground mine at the Strel'tsovskoe U deposit in eastern Transbaikalia. The behaviors of two isotopic U-Pb systems (238U-206Pb and 235U-207Pb) are principally different in all samples from our profile. While the individual samples are characterized by a vast scatter of their T(206Pb/238U) age values (from 112 to 717 Ma), the corresponding T(207Pb/235U) values vary much less significantly (from 127 to 142 Ma) and are generally close to the true age of the U mineralization. The main reason for the distortion of the U-Pb system is the long-lasting (for tens of million years) migration of intermediate decay products in the 238U-206Pb(RD238U) in the samples. This process resulted in the loss of RD238U from domains with high U concentrations and the subsequent accommodation of RD238U at sites with low U concentrations. The long-term effect of these opposite processes resulted in a deficit or excess of 206Pb as the final product of 238U decay. The loss or migration of RD238U are explained by the occurrence of pitchblende in association with U oxides that have higher Si and OH concentrations than those in the pitchblende and a higher +6U/+4U ratio. The finely dispersed character of the mineralization and the loose or metamict texture of the material are the principal prerequisites for RD238U loss and an excess of 206Pb in adjacent domains with low U concentrations. Domains with low U contents in the zone with U mineralization serve as geochemical barriers (because of sulfides contained in them) at which long-lived RD238U(226Ra, 210Po, 210Bi, and 210Pb) were accommodated and subsequently caused an excess of 206Pb. The 235U-207Pb system remained closed because of the much briefer lifetime of the 235U decay products. This may account for the significant discrepancies between the T(206Pb/238U) and T(207Pb/235U) age values. RD238U was most probably lost via the migration of radioisotopes at the middle part and end of the 238U family (starting with 226Ra). The heavy Th, Pa, and U radioisotopes (234Th, 234Pa, 234U, and 230Th) that occur closer to the beginning of 238U decay, before 226Ra, only relatively insignificantly participated in the process. Our results show that the loss and migration of RD238U are, under certain conditions, the main (or even the only) process responsible for the distortion of the U-Pb system. (PUBLICATION ABSTRACT)
机译:在跨贝加利亚东部Strel'tsovskoe U矿床的地下矿山中暴露的U矿化区沿3.5 m剖面采集的矿石材料样品(体积为4至10 cm3)中检测了U-Pb系统。 。根据我们的资料,在所有样品中,两种同位素U-Pb系统(238U-206Pb和235U-207Pb)的行为主要不同。尽管各个样本的特征在于其T(206Pb / 238U)年龄值(从112到717 Ma)的巨大分散,但相应的T(207Pb / 235U)值的变化却不那么明显(从127 Ma到142 Ma),并且通常接近U矿化的真实年龄。 U-Pb系统畸变的主要原因是样品中238U-206Pb(RD238U)中的衰变产物的持久迁移(持续了数千万年)。此过程导致RD238U从高U浓度的域中丢失,并随后将RD238U容纳在低U浓度的位点。这些相反过程的长期影响导致238P衰变的最终产物赤字或过量206Pb。 RD238U的损失或迁移是通过与硅氧化物和OH浓度比在沥青混合料中高的+ 6U / + 4U比的U氧化物结合的混合沥青而发生的。矿物质的精细分散特性和材料的松散或亚变质质地是RD238U损失的主要先决条件,并且在低U浓度的相邻区域中有206Pb过量。 U矿化区中U含量低的区域充当了地球化学屏障(由于其中包含硫化物),在其中容纳了长寿命的RD238U(226Ra,210Po,210Bi和210Pb),随后导致了206Pb的过量。 235U-207Pb系统保持关闭状态,因为235U衰变产物的寿命要短得多。这可能解释了T(206Pb / 238U)和T(207Pb / 235U)年龄值之间的显着差异。 RD238U很可能是由于放射性同位素在238U家族中部和末端(从226Ra开始)的迁移而丢失的。较重的Th,Pa和U放射性同位素(234Th,234Pa,234U和230Th)发生在226Ra之前,更接近238U衰变的开始,仅相对微不足道。我们的结果表明,在某些条件下,RD238U的损耗和迁移是导致U-Pb系统变形的主要(甚至是唯一)过程。 (出版物摘要)

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