Rhodium colloidal suspension deposition on porous silica particles by dry impregnation: Study of the influence of the reaction conditions on nanoparticles location and dispersion and catalytic reactivity

Rhodium composite nanomaterials were synthesized by an innovating process called dry impregnation in a fluidized bed. It consists in spraying an aqueous colloidal suspension of rhodium on silica porous particles. The use of this precursor solution containing preformed nanoparticles avoids calcination/activation step. Different composite nanomaterials were prepared displaying various metal loadings. The operating conditions were tuned to modify τs, the solvent vapour saturation rate value, in order to influence the deposit location: either uniform on the whole silica particles or at the particles surface like a coating. τs is defined as the ratio between solvent content in the bed atmosphere and the maximum solvent content. The obtained samples were investigated in catalytic hydrogenation of aromatic compounds under very mild conditions. Their catalytic performances were compared to those of the original colloidal suspension in one hand and of a similar catalyst prepared through wet impregnation in another hand. Interesting activity and selectivity were observed.This illustrates the interest of the dry impregnation method: this way allows an easy control of the metal loading as well as of the metal loading location in the support particles. Moreover, the support particle size and morphology are preserved

Model arenes hydrogenation with silica-supported rhodium nanoparticles:The role of the silica grains and of the solvent on catalytic activities

Silica-supported rhodium-based nanoheterogeneous catalysts were easily prepared by impregnation with a pre-stabilized colloidal suspension. The resulting catalysts contain rhodium nanoparticles well-dispersed in the silica pores with a mean size of 5 nm. Influence of the silica grains size and of the solvent was investigated in arenes hydrogenation. It appeared that the size of the silica grains has a minimal influence on the reaction rate but the supported nanocatalysts displayed higher TOFs in hexane than in water

High-field and low field magnetoresistance of CoFe nanoparticles elaborated by organometallic chemistry

We report on magnetotransport measurements on CoFe nanoparticles surrounded by an insulating organic layer. Samples were obtained by evaporating a solution of nanoparticles on a patterned substrate. Typical behaviour of Coulomb blockade in array of nanoparticles is observed. High and low field magnetoresistance have been evidenced. Below 10 K, a large high-field magnetoresistance is measured, reaching up to 500 %. Its amplitude decreases strongly with increasing voltage. At 1.6 K, this high-field magnetoresistance vanishes and an inverse low field tunnelling magnetoresistance is observed.Comment: 12 pages, with 3 figures, references and figure captions. Proceeding of the 52nd MMM conferenc

CO2 methanation activated by magnetic heating: life cycle assessment and perspectives for successful renewable energy storage

Purpose Technologies with low environmental impacts and promoting renewable energy sources are required to meet the energetic demand while facing the increase of gas emissions associated to the greenhouse effect and the depletion of fossil fuels. CO2 methanation activated by magnetic heating has recently been reported as a highly efficient and innovative power-to-gas technology in a perspective of successful renewable energy storage and carbon dioxide valorisation. In this work, the life cycle assessment (LCA) of this process is performed, in order to highlight the environmental potential of the technology, and its competitivity with in respect to conventional heating technologies. Methods The IMPACT 2002+ was used for this LCA. The process studied integrates methanation, water electrolysis and CO2 capture and separation. This “cradle-to-gate” LCA study does not consider the use of methane, which is the reaction product. The functional unit used is the energy content of the produced CH4. The LCA was carried out using the energy mix data for the years 2020 and 2050 as given by the French Agency for Environment and Energy management (ADEME). Consumption data were either collected from literature or obtained from the LPCNO measurements as discussed by Marbaix (2019). The environmental impact of the CO2 methanation activated by magnetic heating was compared with the environmental impact of a power-to-gas plant using conventional heating (Helmeth) and considering the environmental impact of the natural gas extraction. Results It is shown that the total flow rate of reactants, the source of CO2 and the energy mix play a major role on the environmental impact of sustainable CH4 production, whereas the lifetime of the considered catalyst has no significant influence. As a result of the possible improvements on the above-mentioned parameters, the whole process is expected to reduce by 75% in its environmental impact toward 2050. This illustrates the high environmental potential of the methanation activated by magnetic heating when coupled with industrial exhausts and renewable electricity production. Conclusions The technology is expected to be environmentally competitive compared with existing similar processes using external heating sources with the additional interest of being extremely dynamic in response, in line with the intermittency of renewable energy production

hcp -Co Nanowires grown on metallic foams as catalysts for Fischer-Tropsch Synthesis

The Fischer-Tropsch synthesis (FTS) is a structure‐sensitive exothermic reaction that enables catalytic transformation of syngas to high quality liquid fuels. Now, monolithic cobalt‐based heterogeneous catalysts were elaborated through a wet chemistry approach that allows control over nanocrystal shape and crystallographic phase, while at the same time enables heat management. Copper and nickel foams have been employed as supports for the epitaxial growth of hcp‐Co nanowires directly from a solution containing a coordination compound of cobalt and stabilizing ligands. The Co/Cufoam catalyst was tested for Fischer-Tropsch synthesis in a fixed‐bed reactor, showing stability and significantly superior activity and selectivity towards C5+ compared to a Co/SiO2‐Al2O3 reference catalyst under the same conditions

Magnetically induced CO2 methanation using exchange‐coupled spinel ferrites in cuboctahedron‐shaped nanocrystals

Magnetically induced catalysis can be promoted taking advantage of optimal heating properties from the magnetic nanoparticles to be employed. However, when unprotected, these heating agents that are usually air-sensitive, get sintered under the harsh catalytic conditions. In this context, we present, to the best of our knowledge, the first example of air-stable magnetic nanoparticles that: 1) show excellent performance as heating agents in the CO2 methanation catalyzed by Ni/SiRAlOx, with CH4 yields above 95 %, and 2) do not sinter under reaction conditions. To attain both characteristics we demonstrate, first the exchange-coupled magnetic approach as an alternative and effective way to tune the magnetic response and heating efficiency, and second, the chemical stability of cuboctahedron-shaped core–shell hard CoFe2O4–soft Fe3O4 nanoparticles.Xunta de Galicia | Ref. IN607 A 2018/5Xunta de Galicia | Ref. ED431C 2016-034Agencia Estatal de Investigación | Ref. CTM2017-84050-

Chemical tuning of Coulomb blockade at room-temperature in ultra-small platinum nanoparticle self-assemblies

This work describes self-assemblies of ultra-small platinum nanoparticles, the electrical properties of which can be adjusted through slight modifications of the assemblies' constituents. Elaborating such systems, stable in air for months, is a first step towards nanoelectronic systems, where the charging energy of the nanoparticles is tuned by the nature of the ligands