There has been a recent push to examine the materials that nature is able to synthesize and consider whether the materials that humans have invented are geomimetic in nature, and whether designing nature-inspired materials is economically and environmentally beneficial. Mesoporous silica represents a class of materials with pore sizes of 2-50 nm and has been studied in catalysis, separations, and drug delivery. It has generally been made using organosilicon precursors, but in this work, we demonstrate for the first time the successful synthesis of mesoporous silica with uniform mesoporosity of 10 nm using the mineral forsterite (Mg2SiO4) as a silica source, providing a potentially cheaper and more Earth-friendly route to making this technologically important material. Forsterite was synthesized by a solid-state chemistry route and underwent dissolution-reprecipitation in an aqueous acid solution containing the soft template surfactant, Pluronic P123. The formation of forsterite was confirmed with X-ray diffraction (XRD), the successful templating of surfactant was demonstrated with thermogravimetric analysis (TGA) and Fourier-transform infrared spectroscopy (FTIR), the surface area was determined through Brunauer-Emmett-Teller (BET) analysis, and pore size and distribution were demonstrated with Barrett-Joyner-Halenda (BJH) analysis. The synthesized mesoporous silica at optimal conditions has surface area of 740 m2/g and pore volume of 1.4 mL/g.

Ammonia is one of the most important chemicals for modern civilization as well as a potentially invaluable intermediary component of a future sustainable H2 economy, yet its current production is decidedly unsustainable. Accordingly, researchers are attempting to devise new paradigms for ammonia production, one of which would involve the cyclical reaction of H2 with a nitride compound and the renitridation of that compound with N2 - a thermochemical loop that would allow for ammonia production with renewable inputs and at relatively low pressures. In this paper, researchers identified several ternary and quaternary metal nitrides with the potential to exhibit relatively favorable thermodynamics for both the reduction and nitridation steps of that reaction cycle. These compounds were synthesized via co-precipitation and Pechini synthesis and several were tested under gas flows of 75% H2/Ar at 100-700 C and 75% H2/N2 at 700 C to determine their behavior under these conditions. As suggested by the available literature, Co3Mo3N was found to be a far better candidate for thermochemical looping than Fe3Mo3N or Ni2Mo3N - with higher mass loss and mass regain. Interestingly, quaternary nitrides containing Fe and Co in addition to Mo also demonstrated remarkable reduction and nitridation capability under ambient pressures. Ultimately, this paper demonstrates the feasibility of synthesizing a variety of single phase ternary and quaternary nitrides and the potential that several of these nitrides hold for producing ammonia sustainably via cyclic thermochemistry.