Sol–Gel Treatments to Flame Retard PA11/Flax Composites

International audienceThis work investigates the efficiency of sol-gel treatments to flame retard flax fabric/PA11 composites. Different sol-gel treatments applied to the flax fabrics were prepared using TEOS in combination with phosphorus and/or nitrogen containing co-precursors (DEPTES, APTES) or additives (OP1230, OP1311). When the nitrogen and the phosphorus co-precursors were used, two coating methods were studied: a 'one-pot' route and a successive layer deposition method. For the "one-pot" method, the three precursors (TEOS, DEPTES, and APTES) were mixed together in the same solutions whereas for the different layers deposition method, the three different treatments were deposited on the fibers successively, first the TEOS, then a mix of TEOS/DEPTES, and finally a mix of TEOS/APTES. After deposition, the sol-gel coatings were characterized using scanning electron microscope, electron probe microanalyzer, and 29 Si and 31 P solid-state NMR. When only TEOS or a mix of TEOS and DEPTES is used, homogeneous coatings are obtained presenting well-condensed Si units (mainly Q units). When APTES is added, the coatings are less homogenous and agglomerates are present. A lower condensation rate of the Si network is also noticed by solid-state NMR. When additives are used in combination with TEOS, the TEOS forms a homogenous and continuous film at the surface of the fibers, but the flame retardants are not well distributed and form aggregates. The flame retardant (FR) efficiency of the different treatments on flax fabrics was evaluated using horizontal flame spread test. The following ranking of the different systems is obtained: TEOS + Additives > TEOS > TEOS + DEPTES~TEOS + DEPTES + APTES > multilayers. All the sol-gel coatings improve the flame retardant properties of the flax fabric, except the multilayer treatment. Based on these results, the three most efficient sol-gels were selected to prepare sol-gel-modified flax/PA11 composites. The composite modified with only TEOS showed the best FR properties. Surprisingly, the composite modified with the phosphorus-based flame retardant (AlPi) did not exhibit improved FR properties. This effect was attributed to the fact that the amount of the FR additive deposited on the fabrics was too low

Adsorption of Orange G Dye on Hydrophobic Activated Bentonite from Aqueous Solution

This report focusses on the modification of physical structure and chemical properties of a bentonite clay from the Hammam Boughrara region of the Maghnia district in western Algeria to maximize its adsorption capacity. The purified bentonite clay (called B) was modified, either by acid activation with 1M sulfuric acid (B-Act), or by intercalation with the cationic surfactant cetytrimethyl ammonium bromide (CTAB), applying a cation exchange capacity (CEC) of 100% (called B-CTAB). Modification of B was also introduced by combining these two steps consecutively, i.e., at first acid activation of B, followed by intercalation with CTAB (B-Act-CTAB). The B-Act-CTAB was obtained by H2SO4 (1M) acid activation, followed by co-adsorption of CTAB with 100% and 300% of the CEC of B-Act as precursor. In particular, a strong increase of surface area and pore volume of the modified bentonites was observed for B-Act (469.83 m²/g and 0.401 cm3g−1), B-Act-CTAB100 (267.72 m²/g and 0.316 cm3 g−1) and B-Act-CTAB300 (111.15 m²/g and 0.171 cm3g−1), compared to B (31.79 m²/g and 0.074 cm3 g−1) and B-CTAB (3.79 m²/g and 0.034 cm3 g−1), respectively. The bentonite-based adsorbents were then used to evaluate the removal efficiency of an organic molecule, the azo dye Orange G (OG), as a model for a Persistent Organic Pollutant. Freundlich, Langmuir and Sips (Langmuir–Freundlich) models were applied to analyze equilibrium isotherms, showing a good correlation between experimental data and the Freundlich model. A good agreement was obtained between experimentally obtained kinetic adsorption data and the pseudo-second-order model, allowing to evaluate rate constants. B-Act-CTAB300 can be applied as a low-cost material for removal of azo dyes, since its adsorption capacity towards OG (102.80 mg/g) exceeds largely that of B-CTAB (31.49 mg/g) and B-Act-CTAB100 (12.77 mg/g)

Adsorption of Orange G Dye on Hydrophobic Activated Bentonite from Aqueous Solution

This report focusses on the modification of physical structure and chemical properties of a bentonite clay from the Hammam Boughrara region of the Maghnia district in western Algeria to maximize its adsorption capacity. The purified bentonite clay (called B) was modified, either by acid activation with 1M sulfuric acid (B-Act), or by intercalation with the cationic surfactant cetytrimethyl ammonium bromide (CTAB), applying a cation exchange capacity (CEC) of 100% (called B-CTAB). Modification of B was also introduced by combining these two steps consecutively, i.e., at first acid activation of B, followed by intercalation with CTAB (B-Act-CTAB). The B-Act-CTAB was obtained by H2SO4 (1M) acid activation, followed by co-adsorption of CTAB with 100% and 300% of the CEC of B-Act as precursor. In particular, a strong increase of surface area and pore volume of the modified bentonites was observed for B-Act (469.83 m²/g and 0.401 cm3g−1), B-Act-CTAB100 (267.72 m²/g and 0.316 cm3 g−1) and B-Act-CTAB300 (111.15 m²/g and 0.171 cm3g−1), compared to B (31.79 m²/g and 0.074 cm3 g−1) and B-CTAB (3.79 m²/g and 0.034 cm3 g−1), respectively. The bentonite-based adsorbents were then used to evaluate the removal efficiency of an organic molecule, the azo dye Orange G (OG), as a model for a Persistent Organic Pollutant. Freundlich, Langmuir and Sips (Langmuir–Freundlich) models were applied to analyze equilibrium isotherms, showing a good correlation between experimental data and the Freundlich model. A good agreement was obtained between experimentally obtained kinetic adsorption data and the pseudo-second-order model, allowing to evaluate rate constants. B-Act-CTAB300 can be applied as a low-cost material for removal of azo dyes, since its adsorption capacity towards OG (102.80 mg/g) exceeds largely that of B-CTAB (31.49 mg/g) and B-Act-CTAB100 (12.77 mg/g)

Selective ligand-free cobalt-catalysed reduction of esters to aldehydes or alcohols

International audienceCobalt(II) salts combined with NaBHEt3 and eventually a base catalyse efficiently and selectively the reduction of esters to aldehydes or alcohols through hydrosilylation by using phenylsilane. Catalyst characterisation by XRD, XPS, TEM and STEM analyses indicates the materials were partially crystalline with the presence of cobalt nanoparticles. Control experiments suggested low valent Co(0) was the active catalytic species involved

Evaluation de la conversion en lit fluidisé dans le cadre du traitement du combustible nucléaire usé

National audienc

Gold(I)-Catalysed Asymmetric Hydroamination of Alkenes: A Silver- and Solvent-Dependent Enantiodivergent Reaction

International audienceIn the present study, we report the first silver dependent enantiodivergent gold catalysed reaction. The asymmetric intramolecular hydroamination of alkenes catalysed by the combination of a single chiral binuclear gold(I) chloride complex and silver perchlorate can afford both enantiomers of the products by a simple solvent change from toluene to methanol. Such an enantiodivergent reaction is strictly independent of the nature of the catalyst anion or the reaction temperature and displays the same first-order kinetic rate law with respect to substrate concentration in both solvents. Beyond a simple solvent effect, the enantioinversion is controlled by gold-silver chloride adducts which occur only in methanol and allow a dual activation of the reagent. While one single gold atom activates the alkene moiety, the other gold atom forms an oxophilic gold-silver chloride adduct which interacts with the carbamate function. By comparison with toluene which affords (S)-enantiomer, this proximal and bimetallic activation allows an opposite stereodifferentiation of the two diastereomeric intermediates during the final protodeauration step and leads therefore to the (R)-enantiomer

ClinMine: Optimizing the Management of Patients in Hospital

International audienceA better understanding of “patient pathway” thanks to data analysis can lead to better treatments for patients. The ClinMine project, supported by the The French National Research Agency (ANR), aims at proposing, from various case studies, algorithmic and statistical models able to handle this type of pathway data, focusing primarily on hospital data. This article presents two of these case studies, focusing on the integration of temporal data within analysis. First, the hypothesis that some aspects of the patient pathway can be described, even predicted, from the management process of the hospital medical mail is studied. Therefore a specific functional data analysis is driven, and several types of patients have been detected. The second case study deals with the detection of profiles through a biclustering of the patients. The difficulty to simultaneously deal with heterogeneous data, including temporal data is exposed and a method is proposed. Results on real data show the effectiveness of the proposed method

Keynote on processing to obtain grain refinement and improved mechanical properties

Peer reviewed: YesNRC publication: Ye