Abstract

Metal nanoparticles (NP) in minerals are an emerging field of research. Development of advanced analytical techniques such as Z-contrast imaging and mapping using high-angle annular dark field scanning transmission electron microscopy (HAADF STEM) allows unparalleled insights at the nanoscale. Moreover, the technique provides a link between micron-scale textures and chemical patterns if the sample is extracted in situ from a location of petrogenetic interest. Here we use HAADF STEM imaging and energy-dispersive X-ray spectrometry (EDX) mapping/spot analysis on focused ion beam prepared foils to characterise atypical Cu-As-zoned and weave-twinned hematite from the Olympic Dam deposit, South Australia. We aim to determine the role of solid-solution versus the presence of discrete included NPs in the observed zoning and to understand Cu-As-enrichment processes. Relative to the grain surface, the Cu-As bands extend in depth as (sub)vertical trails of opposite orientation, with Si-bearing hematite NP inclusions on one side and coarser cavities (up to hundreds of nm) on the other. The latter host Cu and Cu-As NPs, contain mappable K, Cl, and C, and display internal voids with rounded morphologies. Aside from STEM-EDX mapping, the agglomeration of native copper NPs was also assessed by high-resolution imaging. Collectively, such characteristics, corroborated with the geometrical outlines and negative crystal shapes of the cavities, infer that these are opened fluid inclusions with NPs attached to inclusion walls. Hematite along the trails features distinct nanoscale domains with lattice defects (twins, 2-fold superstructuring) relative to hematite outside the trails, indicating this is a nanoprecipitate formed during replacement processes, i.e., coupled dissolution and reprecipitation reactions (CDRR). Transient porosity intrinsically developed during CDRR can trap fluids and metals. Needle-shaped and platelet Cu-As NPs are also observed along (sub)horizontal bands along which Si, Al and K is traceable along the margins. The same signature is depicted along nm-wide planes crosscutting at 60° and offsetting (012)-twins in weave-twinned hematite. High-resolution imaging shows linear and planar defects, kink deformation along the twin planes, misorientation and lattice dilation around duplexes of Si-Al-K-planes. Such defects are evidence of strain, induced during fluid percolation along channels that become wider and host sericite platelets, as well as Cl-K-bearing inclusions, comparable with those from the Cu-As-zoned hematite, although without metal NPs. The Cu-As-bands mapped in hematite correspond to discrete NPs formed during interaction with fluids that changed in composition from alkali-silicic to Cl- and metal-bearing brines, and to fluid rates that evolved from slow infiltration to erratic inflow controlled by fault-valve mechanism pumping. This explains the presence of Cu-As NPs hosted either along Si-Al-K-planes (fluid supersaturation), or in fluid inclusions (phase separation during depressurisation) as well as the common signatures observed in hematite with variable degrees of fluid-mineral interaction. The invoked fluids are typical of hydrolytic alteration and the fluid pumping mechanism is feasible via fault (re)activation. Using a nanoscale approach, we show that fluid-mineral interaction can be fingerprinted at the (atomic) scale at which element exchange occurs.

Highlights

  • The abundance and potential significance of nanoparticles in rocks and ores is gaining recognition, as analytical capabilities expand, allowing detailed characterisation of their physical states and quantification of their chemical compositions

  • This explains the presence of Cu-As NPs hosted either along Si-Al-K-planes, or in fluid inclusions as well as the common signatures observed in hematite with variable degrees of fluid-mineral interaction

  • high-angle annular dark-field (HAADF) scanning transmission electron microscopy (STEM) imaging of the three foils from the zoned Cu-As hematite shows oriented trails tens of microns in length consisting of darker inclusions and cavities (Figures 3 and 4)

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Summary

Introduction

The abundance and potential significance of nanoparticles in rocks and ores is gaining recognition, as analytical capabilities expand, allowing detailed characterisation of their physical states and quantification of their chemical compositions. Metal-bearing nanoparticles (NPs) hosted within minerals, sulphides, have drawn research attention because of their potential economic significance and because they can represent evidence in support of petrogenetic models. Inferences for the presence of discrete Au NPs, alongside lattice-bound (solid solution) gold within arsenian pyrite were validated for the first time by direct imaging of high-As (thousands ppm) pyrite using transmission electron microscopy (TEM) [2]. This type of observation has been used in combination with trace element data to determine an empirical solubility limit for structurally-bound Au in pyrite as a function of increasing

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