The aim of this review article on recent developments of mechanochemistry (nowadays established as a part of chemistry) is to provide a comprehensive overview of advances achieved in the field of atomistic processes, phase transformations, simple and multicomponent nanosystems and peculiarities of mechanochemical reactions. Industrial aspects with successful penetration into fields like materials engineering, heterogeneous catalysis and extractive metallurgy are also reviewed. The hallmarks of mechanochemistry include influencing reactivity of solids by the presence of solid-state defects, interphases and relaxation phenomena, enabling processes to take place under non-equilibrium conditions, creating a well-crystallized core of nanoparticles with disordered near-surface shell regions and performing simple dry time-convenient one-step syntheses. Underlying these hallmarks are technological consequences like preparing new nanomaterials with the desired properties or producing these materials in a reproducible way with high yield and under simple and easy operating conditions. The last but not least hallmark is enabling work under environmentally friendly and essentially waste-free conditions (822 references).

This manuscript reviews the current trends in the recovery of Platinum Group Metals (PGMs) from end-of-life autocatalysts and the aims of the recently funded Marie Sklodowska-Curie Project “Chemistry of Platinum Group Metals-CHemPGM” towards the greening of PGMs recovery processes and the reusing of recovered PGMs for preparation of new catalysts. Together with the analysis of the state of the art recovery of PGMs from spent autocatalysts through pyrometallurgical and hydrometallurgical routes and the recent trends in reducing their environmental impact, also emerging sustainable and green technologies are analyzed. Particular focus is given on the mechanochemical processing as a promising sustainable route not only for the pretreatment of waste materials but also for direct PGMs leaching. The present review identifies also the trends in catalysts for carbon neutrality and the few recent efforts in developing PGM-based catalysts starting directly from the liquor of the leach solutions of spent catalysts envisaging therefore a possible key to close PGMs loop in a more efficient and sustainable way.

Blends of fly ash and natural calcite, mechanically activated for 0–400 s in a planetary mill, were used to synthesize geopolymers at ambient temperature. The calcite content in the blends was 0–10 wt.%. Sodium hydroxide solution was used as an alkaline agent. Mechanical activation of the raw material considerably enhanced its reactivity with respect to the alkaline agent, as was observed using Fourier-transform infrared spectroscopy, isothermal conduction calorimetry, thermogravimetry coupled with mass spectrometry analysis of the evolved gas, and SEM/EDS. The addition of calcite to the fly ash improved the compressive strength of the geopolymers, especially during the early age of curing. For 7 d aged geopolymers based on the 90% fly ash + 10% calcite blend, the strength was 8.0-, 3.5- and 2.9-fold higher than that for the geopolymers based on the unblended fly ash for 30 s, 180 s and 400 s mechanical activation time, respectively. Using Mössbauer spectroscopy, it was revealed that iron present in the fly ash did not play a significant part in the geopolymerization process. The dominant reaction product was sodium containing aluminosilicate hydrogel (N-A-S-H gel). Calcite was found to transform, to a small extent, to vaterite and Ca(OH)₂ in the course of the geopolymerization.