The synthesis of multilayer graphene materials by the fluorination of carbon nanodiscs/nanocones

Multilayer carbonaceous nanomaterial has been synthesized using a two-step process: carbon nanodiscs/nanocones were fluorinated using either the direct reaction with pure F₂ gas or the thermal decomposition of solid fluorinating agent (TbF₄). Then the fluorinated parts were removed by treatment at 600 °C in air. When the fluorine atoms are homogenously dispersed, using fluorination by TbF₄, thinning due to thermal defluorination results in multilayer materials with 7–10 nm of thickness and 400–500 nm of width. Such resulting materials and the fluorinated precursors have been characterized by solid state NMR, TGA, XRD, SEM, TEM, AFM and Raman spectroscopy.     

Nucleation of polystyrene latex particles in the presence of gamma-methacryloxypropyltrimethoxysilane: functionalized silica particles

Silica/polystyrene nanocomposite particles with different morphologies were synthesized through emulsion polymerization of styrene in the presence of silica particles previously modified by gamma-methacryloxypropyltrimethoxysilane (MPS). Grafting of the silane molecule was performed by direct addition of MPS to the aqueous silica suspension in the presence of an anionic surfactant under basic conditions. The MPS grafting density on the silica surface was determined using the depletion method and plotted against the initial MPS concentration. The influence of the MPS grafting density, the silica particles size and concentration and the nature of the surfactant on the polymerization kinetics and the particles morphology was investigated. When the polymerization was performed in the presence of an anionic surfactant, transmission electron microscopy images showed the formation of polymer spheres around silica for MPS grafting densities lower than typically 1 micromole x m(-2) while the conversion versus time curves indicated a strong acceleration effect under such conditions. In contrast, polymerizations performed in the presence of a larger amount of MPS moieties or in the presence of a non ionic emulsifier resulted in the formation of "excentered" core-shell morphologies and lower polymerization rates. The paper identifies the parameters that allow to control particles morphology and polymerization kinetics and describes the mechanism of formation of the nanocomposite colloids.     

3D Investigation of Damage During Strain-Controlled Thermomechanical Fatigue of Cast Al–Si Alloys

The strain-controlled thermomechanical fatigue behavior is investigated for three cast near-eutectic Al–Si alloys with different Ni, Cu, and Mg contents. Synchrotron tomography and neutron diffraction experiments are used to correlate 3D microstructural features with damage initiation and evolution. The results show that the alloy with lower Cu, Ni, and Mg concentrations has up to 45% higher thermomechanical fatigue resistance for cooling/heating rates of 5 and 15 K s⁻¹. In addition, this alloy also exhibits damage formation at later stages during thermomechanical fatigue and slower damage accumulation compared to other alloys. This difference in behavior is a consequence of its higher ductility, which is a result of the lower volume fraction and global interconnectivity of the 3D hybrid networks formed by Si and intermetallics and the absence of large primary Si clusters which act as preferred crack initiation sites during the early stages of thermomechanical fatigue.     

Molecular Regulation of Canalicular ABC Transporters

The ATP-binding cassette (ABC) transporters expressed at the canalicular membrane of hepatocytes mediate the secretion of several compounds into the bile canaliculi and therefore play a key role in bile secretion. Among these transporters, ABCB11 secretes bile acids, ABCB4 translocates phosphatidylcholine and ABCG5/G8 is responsible for cholesterol secretion, while ABCB1 and ABCC2 transport a variety of drugs and other compounds. The dysfunction of these transporters leads to severe, rare, evolutionary biliary diseases. The development of new therapies for patients with these diseases requires a deep understanding of the biology of these transporters. In this review, we report the current knowledge regarding the regulation of canalicular ABC transporters’ folding, trafficking, membrane stability and function, and we highlight the role of molecular partners in these regulating mechanisms.     

Prevalence and characterization of antibiotic resistant Enterococcus faecalis in French cheeses

Prevalence of enterococci and antibiotic resistance profiles of Enterococcus faecalis was analyzed in 126 French cheeses from retail stores. Forty-four percent of pasteurized or thermised-milk cheeses, and up to 92% of raw-milk cheeses contained detectable enterococci. A total of 337 antibiotic resistant enterococci were isolated in 29% and 60% of pasteurized-milk and raw-milk cheeses, respectively. E. faecalis was the predominant antibiotic resistant species recovered (81%), followed by Enterococcus faecium (13%), and Enterococcus durans (6%). The most prevalent antibiotic resistances were tetracycline (Tet) and minocycline (Min), followed by erythromycin (Ery), kanamycin (Kan) and chloramphenicol (Cm). The most common multiple antibiotic resistance phenotype was Cm Ery Kan Min Tet. The occurrence of antibiotic genes, as searched by PCR, was 100 % for aph3′IIIa, 96 % for ermB, 90 % for tetM and 80 % for catA in isolates resistant to Kan, Ery, Tet or Cm, respectively. MLST analysis of 30 multidrug resistant E. faecalis revealed that ST19, CC21, CC25 and CC55 isolates were the most common in cheeses. In conclusion, as in many other European countries, French cheeses do contain enterococci with multiple antibiotics resistances. However, low occurrence of high-level gentamicin resistant or sulfamethoxazole/trimethoprim-resistant enterococci and absence of vancomycin- or ampicillin- resistant enterococci indicate that cheeses cannot be considered as a major reservoir for nosocomial multi-drug resistant enterococci.     

Using X‐Ray Microtomography for Characterisation of Catalyst Particle Pore Structure

The use of a high‐energy synchrotron radiation source has permitted the introduction of high‐resolution X‐ray microtomography imaging as a method of non‐intrusive and non‐destructive three‐dimensional (3D)visualized characterization of porous media. The use of a combination of X‐ray microtomography, along with mercury porosimetry and Low Melting Point Alloy (LMPA) intrusion potentially provides a more complete approach to more accurate catalyst pore structure characterisation and modelling. This combined approach has been applied to the study of an industrial alumina catalysts support. The data collected from the study has been used to develop and generate an improved pore network model basis, in which both heterogeneity and hierarchy are considered in obtaining an improved pore architecture and pore size distribution.     

Generic and reflective graph transformations for checking and enforcement of modeling guidelines

In the automotive industry, the model driven development of software, today considered as the standard paradigm, is generally based on the use of the tool MATLAB Simulink/Stateflow. To increase the quality, the reliability, and the efficiency of the models and the generated code, checking and elimination of detected guideline violations defined in huge catalogs has become an essential task in the development process. It represents such a tremendous amount of boring work that it must necessarily be automated. In the past we have shown that graph transformation tools like Fujaba/MOFLON allow for the specification of single modeling guidelines on a very high level of abstraction and that guideline checking tools can be generated from these specifications easily. Unfortunately, graph transformation languages do not offer appropriate concepts for reuse of specification fragments—a MUST, when we deal with hundreds of guidelines. As a consequence we present an extension of MOFLON that supports the definition of generic rewrite rules and combines them with the reflective programming mechanisms of Java and the model repository interface standard Java Metadata Interface (JMI).     

Mechanism of carbon–nitrogen bond scission in the presence of H2S on Pt Supported catalysts

The reactivity of a series of amines with various structures and different numbers of hydrogen atoms on the carbon atoms in the and position was used to evidence the C–N bond scission mechanism in the presence of H₂S on Pt based catalysts (deposited on alumina, zirconia and silica–alumina) and compare it with the mechanism on a NiMoP on alumina sulfide catalyst. The effect of the H₂S partial pressure was also checked. Catalytic activities (amine overall conversion, C₅ hydrocarbon formation, and amine disproportionation) deeply depend on the structure of the N-containing molecule. Tert-pentylamine is the most reactive molecule for sulfide catalysts whereas, in the case of n-pentylamine, Pt on zirconia was found to be the most efficient for C–N bond breaking. Such properties cannot be related to the acidic properties of the support but to a unique support–metal interaction, since alumina or silica–alumina supported platinum catalysts do not present this behaviour.