Porphyry copper mineralization triggered by sulfate reduction and alkali metasomatism: Constraints from an experimental investigation

GSA Bulletin Pub Date : 2023-01-10 DOI:10.1130/b36435.1
Jianping Li, Weihua Liu, Long Su, Dengfeng Li, Shitao Zhang, Huayong Chen
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Abstract

The potassium silicate (K-silicate) alteration zone is the main ore contributor in porphyry copper deposits worldwide. Knowledge of element behaviors in the alteration and mineralization processes is essential for an improved understanding of porphyry copper mineralization, but they are still not well understood. In this study, we reacted synthetic Cl-rich fluids, containing K, Na, Cu, Mo, Zn, etc., with andesite in a complex experimental system to simulate the shallow porphyry copper mineralization process. We aimed to bridge the gap between simple experimental studies and complex natural systems and to evaluate the contribution of sulfate reduction to porphyry ore formation and its relationship with early alkali metasomatism. The results show that increasing temperature (from 300 to 500 °C) enhances the K-silicate alteration by promoting ion-exchange reactions, and the K-feldspar is mainly formed by the transformation of plagioclase via a dissolution-reprecipitation processes. The low-salinity vapor phase has a stronger capacity for K-silicate alteration than the liquid phase at similar temperatures. In addition, increasing temperature from 300 to 500 °C favors sulfate reduction to further enhance metal sulfide precipitation. The limited availability of reduced sulfur in the fluid causes preferential precipitation of Cu-(Mo) sulfides, while most of the Zn is soluble in the fluid, and Cu precipitation as sulfides in the vapor is much more efficient than in the coexisting liquid. The overlap between the K-silicate alteration zone and the mineralization triggered by sulfate reduction in porphyry copper deposits is controlled by several concomitant factors, e.g., relatively high temperature (e.g., at 400−500 °C), vapor formation, and decompression. Moreover, K-silicate alteration would further promote mineralization by changing fluid compositions, e.g., removing K from the fluid.
硫酸盐还原和碱交代引发的斑岩铜矿化:来自实验研究的约束
硅酸钾蚀变带是世界范围内斑岩型铜矿床的主要矿源。了解蚀变和成矿过程中的元素行为对于提高对斑岩铜成矿作用的认识是必不可少的,但它们仍然没有得到很好的理解。本研究在复杂的实验系统中,合成含K、Na、Cu、Mo、Zn等富cl流体与安山岩反应,模拟浅层斑岩铜矿化过程。我们旨在弥合简单的实验研究与复杂的自然系统之间的差距,并评估硫酸盐还原对斑岩成矿的贡献及其与早期碱交代的关系。结果表明:温度升高(300 ~ 500℃)通过促进离子交换反应促进了钾硅酸盐的蚀变,钾长石主要由斜长石的溶蚀-再沉淀过程转化而成。在相同温度下,低盐度气相比液相具有更强的钾硅酸盐蚀变能力。此外,温度从300℃升高到500℃有利于硫酸盐还原,进一步增强金属硫化物的析出。流体中有限的还原硫导致Cu-(Mo)硫化物优先沉淀,而大多数Zn在流体中是可溶的,并且Cu在蒸气中以硫化物的形式沉淀比在共存的液体中更有效。钾硅酸盐蚀变带与斑岩铜矿中硫酸盐还原引起的矿化作用重叠,受高温(400 ~ 500℃)、蒸汽形成和减压等伴生因素控制。此外,钾硅酸盐蚀变将通过改变流体成分(例如从流体中去除钾)进一步促进矿化。
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