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Amorphous silica is a common precipitate in modern and ancient hot springs and in geothermal power plants, yet the corresponding precipitation rates and mechanisms are still highly debated, primarily due to the plethora of parameters that can affect the reactions in natural waters. Here, we report the results from a first ever industrial-scale time-resolved (1 day to 10 weeks) study of silica precipitation conducted at the Hellisheiði geothermal power plant (SW-Iceland). We show that such in-work pipelines of a geothermal power plant are ideal environments to investigate silica precipitation because the physicochemical conditions are well constrained and con-2 stantly monitored. Our results document that amorphous silica forms via two distinct precipitation modes: (1) the fast deposition of continuous botryoidal silica layers and (2) the growth of 3D fan-or ridge-shaped silica aggregates. The continuous layers grow by heterogeneous nucleation and subsequent surface controlled growth by monomer addition. In contrary, the 3D aggregates form through homogeneous nucleation of silica nano-and microparticles in solution, followed by deposition and cementation on the surface of the botryoidal layer. From the time-resolved data, silica precipitation rates of over 1 g m-2 day-1 are derived. Over time, this deposition of silica on pipelines and fluid handling equipment is detrimental to geothermal power production. Our data does not only help improve our understanding of silica precipitation from geothermal fluids, but the determined silica precipitation mechanisms and rates help improve mitigation strategies against silica scaling inside in-work geothermal power plants.

Interactions between silica and proteins are crucial for the formation of biosilica and the production of novel functional hybrid materials for a range of industrial applications. The proteins control both precipitation pathway and the properties of the resulting silicaorganic composites. Here, we present data on the formation of silica-lysozyme composites through two different synthesis approaches (co-precipitation vs. adsorption) and show that the chemical and structural properties of these composites, when analyzed using a combination of synchrotron-based scattering (total scattering and small-angle X-ray scattering), spectroscopic, electron microscopy, and potentiometric methods vary dramatically. We document that while lysozyme was not incorporated into nor did its presence alter the molecular structure of silica, it strongly enhanced the aggregation of silica particles due to electrostatic and potentially hydrophobic interactions, leading to the formation of composites with characteristics differing from pure silica. The differences increased with increasing lysozyme content for both synthesis approaches. Yet, the absolute changes differ substantially between the two sets of composites, as lysozyme did not just affect aggregation during co-precipitation but also particle growth and likely polymerization during co-precipitation. Our results improve the fundamental understanding of how organic macromolecules interact with dissolved and nanoparticulate silica and how these interactions control the formation pathway of silica-organic composites from sodium silicate solutions, a widely available and cheap starting material.

A quantitative understanding of aggregation mechanisms leading to the formation of composites of inorganic nanoparticles (NPs) and proteins in aqueous media is of paramount interest for colloid chemistry. In particular, the interactions between silica (SiO2) NPs and lysozyme (LZM) have attracted attention, because LZM is well-known to adsorb strongly to silica NPs, while at the same time preserving its enzymatic activity. The inherent nature of the aggregation processes leading to NP–LZM composites involves structural changes at length scales from few to at least hundreds of nanometres but also time scales much smaller than one second. To unravel these we used in situ synchrotron-based small-angle X-ray scattering (SAXS) and followed the subtle interparticle interactions in solution at a time resolution of 50 ms/frame (20 fps). We show that if the size of silica NPs (ca. 5 nm diameter) is matched by the dimensions of LZM, the evolving scattering patterns contain a unique structure-factor contribution originating from the presence of LZM. We developed a scattering model and applied it to analyse this structure function, which allowed us to extract structural information on the deformation of lysozyme molecules during aggregation, as well as to derive the mechanisms of composite formation.