Who You Gonna Call?: Creating a Call List for Your Facility\u27s Disaster Plan

Preservation can involve responding to active and pressing matters. But not all buildings are lost to the bulldozer. Many are lost to natural and human disasters like storms and water. A Disaster Plan is a common document used by museums and history organizations. Learn how to develop a contact list for a Disaster Response Plan so you know whom to call when disaster strikes

Eco-Friendly Synthesis of Nitrogen-Doped Mesoporous Carbon for Supercapacitor Application

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Bacterial Colonization of Low‐Wettable Surfaces is Driven by Culture Conditions and Topography

Effect of surface low‐wettability on bacterial colonization has become a prominent subject for the development of antibacterial coatings. However, bacteria's fate on such surfaces immersed in liquid as well as causal factors is poorly understood. This question is addressed by using a range of coatings with increasing hydrophobicity, to superhydrophobic, obtained by an atmospheric plasma polymer method allowing series production. Chemistry, wettability, and topography are thoroughly described, as well as bacterial colonization by in situ live imaging up to 24 h culture time in different liquid media. In the extreme case of superhydrophobic coating, substrates are significantly less colonized in biomolecule‐poor liquids and for short‐term culture only. Complex statistical analysis demonstrates that bacterial colonization on these low‐wettable substrates is predominantly controlled by the culture conditions and only secondary by topographic coating's properties (variation in surface structuration with almost constant mean height). Wettability is less responsible for bacterial colonization reduction in these conditions, but allows the coatings to preserve colonization‐prevention properties in nutritive media when topography is masked by fouling. Even after long‐term culture in rich medium, many large places of the superhydrophobic coating are completely free of bacteria in relation to their capacity to preserve air trapping

Elaboration of Highly Modified Stainless Steel/Lead Dioxide Anodes for Enhanced Electrochemical Degradation of Ampicillin in Water

Lead dioxide-based electrodes have shown a great performance in the electrochemical treatment of organic wastewater. In the present study, modified PbO2 anodes supported on stainless steel (SS) with a titanium oxide interlayer such as SS/TiO2/PbO2 and SS/TiO2/PbO2-10% Boron (B) were prepared by the sol–gel spin-coating technique. The morphological and structural properties of the prepared electrodes were characterized by scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), and X-ray photoelectron spectroscopy (XPS). It was found that the SS/TiO2/PbO2-10% B anode led to a rougher active surface, larger specific surface area, and therefore stronger ability to generate powerful oxidizing agents. The electrochemical impedance spectroscopy (EIS) measurements showed that the modified PbO2 anodes displayed a lower charge transfer resistance Rct. The influence of the introduction of a TiO2 intermediate layer and the boron doping of a PbO2 active surface layer on the electrochemical degradation of ampicillin (AMP) antibiotic have been investigated by chemical oxygen demand measurements and HPLC analysis. Although HPLC analysis showed that the degradation process of AMP with SS/PbO2 was slightly faster than the modified PbO2 anodes, the results revealed that SS/TiO2/PbO2-10%B was the most efficient and economical anode toward the pollutant degradation due to its physico-chemical properties. At the end of the electrolysis, the chemical oxygen demand (COD), the average current efficiency (ACE) and the energy consumption (EC) reached, respectively, 69.23%, 60.30% and 0.056 kWh (g COD)−1, making SS/TiO2/PbO2-10%B a promising anode for the degradation of ampicillin antibiotic in aqueous solutions

Large-scale synthesis of fluorinated graphene by rapid thermal exfoliation of highly fluorinated graphite

International audienceWeakly fluorinated graphene nanosheets were efficiently prepared via fast thermal exfoliation of highly fluorinated graphite. This scalable method consists of a fast temperature increase (around 10 °C s−1) of fluorinated HOPG performed under an argon atmosphere, without any post-treatment. The mechanism of exfoliation induced by the defluorination step, evolving volatile fluorocarbons, has been highlighted thanks to thermogravimetric analysis (TGA), high temperature X-ray diffraction (HTK-XRD), X-ray Photoelectron Spectrometry (XPS) studies on temperature, and Raman and infrared spectroscopy. The advantages of the described process are its high-yield for the preparation of fluorinated graphene nanosheets, its ease of implementation and scalability. Moreover, the fluorine content drastically decreases during such a process and graphene layers are slightly functionalized, i.e. conductive contrary to the precursor

Deep-UV laser direct writing of photoluminescent ZnO submicron patterns: an example of nanoarchitectonics concept

International audienceMicro- and nanopatterning of metal oxide materials is an important process to develop electronic or optoelectronic devices. ZnO is a material of choice for its semiconducting and photoluminescence properties. In the frame of the nanoarchitectonics concept, we have developed and investigated a new process that relies on direct writing laser patterning in the Deep-UV (DUV) range to prepare photoluminescent microstructures of ZnO at room temperature, under air. This process is based on a synthesis of colloidal ZnO nanocrystals (NCs) with a careful choice of the ligands on the surface to obtain an optimal (i) stability of the colloids, (ii) redissolution of the non-insolated parts and (iii) cross-linking of the DUV-insolated parts. The mechanisms of photocrosslinking are studied by different spectroscopic methods. This room temperature process preserves the photoluminescence properties of the NCs and the wavelength used in DUV allows to reach a sub-micrometer resolution, which opens new perspectives for the integration of microstructures on flexible substrates for optoelectronic applications

Study of carbon-flax hybrid composites modified by fibre fluorination

International audienceKnowing that fibre reinforced polymers are sensitive to moisture through their interphases, carbon and flax fibres sized with Bisphenol A diglycidyl ether were fluorinated under a N2/F2 atmosphere. Because of differences in reactivity of gaseous F2 between fibres and sizing, only the latter has been fluorinated, resulting in a covalent grafting of fluorine atoms onto the fibres, that has been evidenced by Infrared spectroscopy, and X-Ray Photoelectron Spectroscopy. Fluorinated fibres exhibit enhanced mechanical properties, as highlighted by tensile tests. Hybrid and non-hybrid composite materials were then fabricated with vacuum infusion process, using non-fluorinated and fluorinated carbon and flax fibres. Their hydrothermal behaviour and mechanical properties were investigated, in order to study the impact of both hybridisation and fibre fluorination on the composite properties. A better water resistance was observed for polymer materials reinforced with fluorinated fibres, whereas their mechanical properties were slightly lower than polymers reinforced with non-fluorinated fibres