The occurrence of exGR-Fe(III)* transient compounds (marked as ‘oxidized volume’ in Figure 6), keeping temporarily the conductive structure of green rust, may explain the observed high learn more reaction rates; these exGR-Fe(III)* transient compounds were fully evidenced by voltammetry in our previous works [19, 22]. Whatever the R values are, the samples display mass values that are in consistency with Equations 2 and 3. The metal loads that can be obtained from our method are between 0 and the maximal theoretical values,

25.2% for Au/exGRs-Fe(III), 29.2% for Au/exGRc-Fe(III), 35.6% for Ag/exGRs-Fe(III), and up to 40.4% for Ag/exGRc-Fe(III). These load values are very high and should even be increased after calcination to hematite α-Fe2O3. Figure 6 Cross-sectional schematic of Au III /GR reaction. With only one final separation step and the use of non-hazardous reagents, the synthesis of our ��-Nicotinamide metal/exGR-Fe(III) S3I-201 nanohybrids is very attractive. Due to their flat shape,

the nanohybrids can be easily separated from a solution by filtration, either after their synthesis or after their operation as colloidal reagents. Moreover, their manipulation is very easy and relatively safe since mineral types such as iron compounds are generally fully biocompatible and metal nanoparticles are well attached to the inorganic matrices. The surface of inorganic and/or metal parts can be functionalized to target specific Selleckchem Alectinib properties. The nanohybrids can be compacted to build permeable reactive membranes for remediation or disinfection treatments and heterogeneous catalysis. The formation of thin films by cast deposition, for example, may also be considered for the fabrication of modified (bio-) electrodes dedicated

to analytical applications. If necessary, the inorganic part could even be partially or entirely removed by acidic or reducing treatments. This facile removal is attractive when the device requires metal nanoparticles only. Conclusion The paper reports a new, simple, and fast (40 min) one-pot synthesis of supported Au and Ag nanoparticles in which a reactive Fe(II)-bearing green rust inorganic particle is used as an individual micro-reactor acting as both the reducing agent and the support for the resulting metal nanoparticles. The reaction of carbonate or sulfate green rusts with AuCl4 − or Ag(NH3)2 + involves the solid-state oxidation of green rust, and the reduction/precipitation onto the inorganic surface of Au or Ag metal. The resulting nanohybrids display a platy shape inorganic part, similar to the green rust precursor, supporting about one to ten metal nanoparticles which appear as flattened hemispheres (Au) or as polyhedrons (Ag). The size ranges are 10 to 60 nm for sulfate green rust and 20 to 120 nm for carbonate green rust.