However, the mineral samples available for laboratory experiments usually display very large dimensions, which preclude any potential applications. Green rusts (GR) are layered FeII-FeIII hydroxisalts composed of positively charged Fe(OH)6 octahedra sheets alternating

with interlayers filled with charge-compensating Salubrinal Microtubule Associated inhibitor anions and water molecules [13]. Early studies on the reduction of AgI or AuIII by green rusts were reported in 2003, from Heasmann et al. and O’Loughlin et al. [14, 15]. The presence of Au or Ag metal was evidenced by X-ray absorption spectroscopy and transmission electron microscopy. Later, these green rusts doped with very low metal loads were utilized as reducing compounds for the removal of some chlorinated hydrocarbons [16, 17]. In these studies, the reaction mechanisms between green rust and soluble

metal precursor were not detailed and none of the studies gave an evidence of metallic particles by X-ray diffraction (XRD). The proposed mechanism involves the oxidation of sulfate green rust into magnetite Fe3O4, coupled to the reduction of AuIII or AgI to Au or Ag. The oxidation mechanisms of green rusts have been extensively studied. This reaction can imply transformations via solution, i.e., dissolution, oxidation, and precipitation of the resulting ferric oxy-hydroxides, lepidocrocite, and goethite [18, 19]. Otherwise, a solid-state oxidation SAHA HDAC order of green rusts involving both the conversion of FeII to FeIII inside the crystal lattice and the charge-compensating loss of protons is also possible [19–22]. The latter mechanism especially occurs when high oxidation rate is imposed, for example, by reaction with some soluble oxidizers such as H2O2. The resulting ferric products, named as ‘exGR-Fe(III)’ or as ‘ferric green rust’, keep the same apparent morphology Resminostat as the initial green rusts; only local disorders at nanometric scale are induced, as indicated by the disappearance or the large

decrease of (00l) lines in diffraction patterns [19, 21, 22]. In the present paper, we introduce a new one-pot synthesis of supported noble metal nanoparticles in which the green rust particle is an individual micro-reactor acting as both the reducing agent and the support for the resulting metal nanoparticles. Carbonate (GRc) or sulfate (GRs) green rust suspensions were obtained from the oxidation by air of slightly alkaline solutions containing ferrous species and carbonate or sulfate anions and the reactions with AuIII or AgI were operated shortly after, in the same solution [23]. Our purpose is the production of Au or Ag nanoparticles by this new method and we therefore target high metal loads. This simple synthesis is carried out at near ambient temperature, in aqueous solution, and requires only common salts; it is environment friendly since no organic solvents/additives are used and the filtrates do not represent a problem for recycling.