Cyril Aymonier

Hybrids of silver nanoparticles with amphiphilic hyperbranched macromolecules exhibiting antimicrobial properties

Hybrids of silver particles of 1 to 2 nm in size with highly branched amphiphilically modified polyethyleneimines adhere effectively to polar substrates providing environmentally friendly antimicrobial coatings.

Current and foreseeable applications of supercritical water for energy and the environment.

It is crucial to develop economical and energy-efficient processes for the sustainable transformation of biomass into fuels and chemicals. In this context, supercritical water biomass valorization (SCBV) processes are an alternative way to produce biogas, biofuels, and valuable chemicals. Supercritical water technology has seen much progress over the last fifteen years and an industrial application has merged: the supercritical water oxidation of wastes. The evolution from lab-scale to pilot-scale facilities has provided data on reaction mechanisms, kinetics, modeling, and reactor technology as well as an important know-how, which can now be exploited to use the reactivity in supercritical water to transform biomass into gases (CO, H(2), CO(2), CH(4), and N(2)) or into liquids (liquid fuel and valuable chemicals) with the supercritical water biomass gasification and liquefaction processes, respectively. This Review highlights the potential of SCBV processes to transform biomass into gas and liquid energy sources and highlights the developments that are still necessary to push this technology onto the market.

Near- and Supercritical Alcohols as Solvents and Surface Modifiers for the Continuous Synthesis of Cerium Oxide Nanoparticles

Supercritical fluids offer fast and facile routes toward well-crystallized tailor-made cerium oxide nanoparticles. However, the use of surfactants to control morphology and surface properties remains essential. Therefore, although water, near-critical (nc) or supercritical (sc), is a solvent of choice, the poor water solubility of some surfactants could require other solvent systems such as alcohols, which could themselves behave as surface modifiers. In here, the influence of seven different alcohols, MeOH, EtOH, PrOH, iPrOH, ButOH, PentOH, and HexOH, in alcothermal conditions (300 °C, 24.5 MPa) over CeO(2) nanocrystals (NCs) size, morphology, and surface properties was investigated. The crystallite size of the CeO(2) nanocrystals can be tuned in the range 3-7 nm depending on the considered alcohol, and their surface has been modified by these solvents without the use of surfactants. Mechanisms are proposed for the interaction of primary and secondary alcohols with CeO(2) surface and its functionalization during the synthesis based on FTIR and TGA-MS studies. This study allows apprehending the role of alcohols during the synthesis and may lead to an informed choice of solvent as a function of the required size and surface properties of CeO(2) NCs. It also opens new route to CeO(2) functionalization using supercritical alcohol derivatives.

Single-step synthesis of well-crystallized and pure barium titanate nanoparticles in supercritical fluids

Single-step synthesis of ultra-fine barium titanate powder with a crystallinity as high as 90% and without barium carbonate contamination has been successfully performed under supercritical conditions using a continuous-flow reactor in the temperature range 150–380 °C at 16 MPa. To synthesize this bimetallic oxide, alkoxides, ethanol and water were used. The influence of the synthesis parameters on the BaTiO3 powder characteristics was investigated. The results show that the water to alkoxide precursor ratio, the reactor temperature and the Ba:Ti molar ratio of alkoxide precursor play a major role in the crystallization of pure and well-crystallized BaTiO3 nanoparticles. The continuous mode of operation without post-treatments for powder washing, drying or crystallization increase the industrial interest.

Synthesis of nanostructured materials in supercritical ammonia: nitrides, metals and oxides

In this study, the synthesis of nanostructured particles of nitrides (Cr2N, Co2N, Fe4N, Cu3N, Ni3N), metal (Cu) and oxides (Al2O3, TiO2, Ga2O3) by using supercritical ammonia in the reaction medium is described. The elaboration process is based on the thermal decomposition of metal precursors in a supercritical ammonia–methanol mixture at a range of temperatures between 170 and 290 °C at about 16 MPa. Nitrides are obtained at relatively low temperatures in comparison with classical processes. It is shown that the chemical composition of the produced materials can be controlled by the adjustment of process operating conditions (pressure, temperature, metal precursor concentration and residence time in the elaboration reactor) and by the knowledge of the Gibbs free energy of oxide formation of the studied metal.

In Situ IR Spectroscopy and Ab Initio Calculations To Study Polymer Swelling by Supercritical CO2

The CO(2) sorption and polymer swelling of hydroxytelechelic polybutadiene (HTPB) and poly(ethylene glycol) (PEG) have been investigated as a function of temperature and CO(2) pressure by combining in situ near-infrared spectroscopy with molecular modeling. The results reported here for the PEG-CO(2) system are in a very good agreement with literature data hence validating our experimental procedure. It has been found that CO(2) sorption and swelling effect is more important for PEG than for HTPB. For both polymers, an increase of temperature leads to a strong decrease of both the CO(2) sorption and swelling. In order to identify at a molecular level the nature and strength of intermolecular interaction occurring between CO(2) and the polymers, ab initio calculations have been performed on model structures, representative of the main functional group of the polymer, and their complex with CO(2). Trans-3-hexene (3-Hex), propyl methyl ether (PME) and methoxytrimethylsilane (MTMS) have been selected to mimic the functional groups of HTPB, PEG and polydimethyl siloxane (PDMS), respectively. The last system has been chosen since previous works on the swelling of PDMS by high pressure CO(2) have revealed the high ability of CO(2) to swell both uncrosslinked and crosslinked PDMS. The calculated stabilization energies of the MTMS-CO(2), PME-CO(2), and 3-Hex-CO(2) dimers indicate that CO(2) interacts specifically with the three moieties through a Lewis acid-Lewis base type of interaction with the energies displaying the following order: E(MTMS-CO(2)) = -3.59 > E(PME-CO(2)) = -3.43 > E(3-Hex-CO(2)) = -2.5 kcal/mol. Since the solubility of CO(2) in the corresponding homopolymers follows the same order, it is evidenced that the stronger the interaction between CO(2) and the polymer, the higher the CO(2) sorption. Therefore, even if one cannot exclude the influence of free volume and chain flexibility of the polymer, it appears that the solubility of CO(2) in the polymer is predominantly governed by the interaction between CO(2) and the polymer. Although the same trend is observed for the swelling of the polymer as a function of the CO(2) pressure, we have found that for a given value of CO(2) sorption, the swelling of the polymer depends on its nature, meaning that the swelling is not only governed by the CO(2)-polymer interaction but also by other intrinsic properties of the polymer.

Dripping to jetting transitions observed from supercritical fluid in liquid microcoflows

Dripping to jetting transition from liquid-liquid to liquid-gas systems has been widely studied in microfluidics. Recent developments have permitted the use of supercritical fluids at high pressure and various temperatures in microfluidic systems to develop sustainable processes. In this article, we use this strategy to demonstrate the possibility to generate stable droplets and reversible dripping to jetting transitions at microscale from supercritical carbon dioxide-liquid water microcoflows.

CeO2 Nanocrystals from Supercritical Alcohols: New Opportunities for Versatile Functionalizations?

The fast and controlled synthesis of surface-modified cerium oxide nanoparticles was carried out in supercritical {ethanol + alcohol derivative} mixtures. The newly found ability of supercritical alcohols to graft onto cerium oxide nanocrystals (CeO2 NCs) during their synthesis was exploited to control their surface chemistry via the addition of three aminoalcohols: ethanolamine, 3-amino-1-propanol and 6-amino-1-hexanol. Although the ethanol to aminoalcohol ratio was consistent (285:1), the successful grafting of these alcohol derivatives onto CeO2 NCs was identified based on Fourier transform infrared (FTIR) and thermogravimetric analysis-mass spectrometry (TGA-MS) measurements. Smaller crystallite size of CeO2 NCs synthesized in the presence of aminoalcohols, compared to those synthesized in supercritical ethanol alone, were also noticed and attributed to a possible intervention of amine groups helping the grafting of the alcohols, allowing one to stop the growth of the CeO2 NCs faster. The use of supercritical alcohol mixture-ethanol with hexanol, dodecanol, or octadecanol, with a 285:1 ratio-was also investigated. Such mixtures allow accessing a finer control in CeO2 NCs crystallite size compared to pure alcohols, according to calculation made from X-ray diffraction measurements. Finally, fluorescent molecules (fluorescein isothiocyanate) were grafted onto amine-modified CeO2 NCs. The powders displayed a fluorescent behavior under UV light, confirming the suitability and interest of CeO2 NCs surface modification by such technique.

Microfluidic Synthesis of Palladium Nanocrystals Assisted by Supercritical CO2: Tailored Surface Properties for Applications in Boron Chemistry

On the surface: A library of organic-inorganic hybrid palladium nanocrystals was synthesized using continuous supercritical microfluidic technology. The nanocatalysts show moderate to excellent activities towards C(Ar)-B and C(Ar)-C(Ar) bond-forming reactions, thus illustrating the relationship between surface properties and modulated catalytic activity.

Self-assembled composite nano-materials exploiting a thermo reversible n-acene fibrillar scaffold and organic-capped ZnO nanoparticles

An organic–inorganic composite material is obtained by self-assembly of 2,3-didecyloxy-anthracene (DDOA), an organogelator of butanol, and organic-capped ZnO nanoparticles (NPs). The ligand 3, 2,3-di(6-oxy-n-hexanoic acid)-anthracene, designed to cap ZnO and interact with the DDOA nanofibers by structural similarity, improves the dispersion of the NPs into the organogel. The composite material displays mechanical properties similar to those of the pristine DDOA organogel, but gelates at a lower critical concentration and emits significantly less, even in the presence of very small amounts of ZnO NPs. The ligand 3 could also act as a relay to promote the photo-induced quenching process.