A MEMS-based solid propellant microthruster array for space and military applications

Since combustion is an easy way to achieve large quantities of energy from a small volume, we developed a MEMS based solid propellant microthruster array for small spacecraft and micro-air-vehicle applications. A thruster is composed of a fuel chamber layer, a top-side igniter with a micromachined nozzle in the same silicon layer. Layers are assembled by adhesive bonding to give final MEMS array. The thrust force is generated by the combustion of propellant stored in a few millimeter cube chamber. The micro-igniter is a polysilicon resistor deposited on a low stress SiO2/SiNx thin membrane to ensure a good heat transfer to the propellant and thus a low electric power consumption. A large range of thrust force is obtained simply by varying chamber and nozzle geometry parameters in one step of Deep Reactive Ion Etching (DRIE). Experimental tests of ignition and combustion employing home made (DB+x% BP) propellant composed of a Double-Base and Black-Powder. A temperature of 250 therefore degrees C, enough to propellant initiation, is reached for 40 mW of electric power. A combustion rate of about 3.4 mm/s is measured for DB+20% BP propellant and thrust ranges between 0.1 and 3,5 mN are obtained for BP ratio between 10% and 30% using a microthruster of 100 mu m of throat wide

Dioxygen activation with a cytochrome P450 model. Characterization and electrochemical study of new unsymmetrical tetradentate Schiff-base complexes with iron(III) and cobalt(II)

Salicylaldehyde or 5-bromosalicylaldehyde react with 2,3-diaminophenol to give two unsymmetrical Schiff-bases H2L1, H2L2, respectively. With Fe(III) and Co(II), these ligands lead to four complexes: Fe(III)ClL1, Fe(III)ClL2, Co(II)L1, Co(II)L2. The structures of these complexes were determined by mass spectroscopy, infrared and electronic spectra. Cyclic voltammetry in dimethylformamide (DMF) showed irreversible waves for both ligands. In the same experimental conditions, Fe(III)ClL1 exhibited a reversible redox couple Fe(III)/Fe(II) while the three other complexes showed quasi-reversible systems. The behavior of some of these complexes in the presence of dioxygen and the comparison with cytochrome P450 are described

Population dynamics of Anopheles gambiae s.l. in Bobo-Dioulasso city: bionomics, infection rate and susceptibility to insecticides.

Published onlineJournal ArticleResearch Support, Non-U.S. Gov'tBACKGROUND: Historical studies have indicated that An. gambiae s.s. is the predominant malaria vector species in Bobo-Dioulasso the second biggest city of Burkina Faso (West Africa). However, over the last decade, An. arabiensis appears to be replacing An. gambiae s.s. as the most prevalent malaria vector in this urban setting. To investigate this species transition in more detail the present study aims to provide an update on the malaria vector composition in Bobo-Dioulasso, and also the Plasmodium infection rates and susceptibility to insecticides of the local An. gambiae s.l. population. METHODS: An entomological survey was carried out from May to December 2008 in Dioulassoba and Kodeni (central and peripheral districts respectively), which are representative of the main ecological features of the city. Sampling consisted of the collection of larval stages from water bodies, and adults by monthly indoor residual spraying (IRS) using aerosol insecticides. Insecticide susceptibility tests were performed using the WHO filter paper protocol on adults emerged from larvae. PCR was used to determine vector species and to identify resistance mechanisms (kdr and ace-1(R)). The Plasmodium infection rate was estimated by ELISA performed on female mosquitoes collected indoors by IRS. RESULTS: An. arabiensis was found to be the major malaria vector in Bobo-Dioulasso, comprising 50 to 100% of the vector population. The sporozoite infection rate for An. arabiensis was higher than An. gambiae s.s. at both Dioulassoba and Kodeni. An. gambiae s.l. was resistant to DDT and cross-resistant to pyrethroids at the two sites with higher levels of resistance observed in An. gambiae s.s. than An. arabiensis. Resistance to 0.1% bendiocarb was observed in the An. gambiae s.s. S form but not the M form or in An. arabiensis. The L1014F kdr mutation was detected in the two molecular forms of An. gambiae s.s. at varying frequencies (0.45 to 0.92), but was not detected in An. arabiensis, suggesting that other mechanisms are involved in DDT resistance in this species. The ace-1(R) mutation was only detected in the S molecular form and was observed at the two sites at similar frequency (0.3). CONCLUSIONS: Over the last ten years, An. arabiensis has become the major malaria vector in Bobo-Dioulasso city where it was formerly present only at low frequency. However, the ecological determinant that enhances the settlement of this species into urban and peri-urban areas of Bobo-Dioulasso remains to be clarified. The impact of the changing An. gambiae s.l. population in this region for vector control including resistance management strategies is discussed.CORUS 6015MIM 60098

High binding yet accelerated guest rotation within a cucurbit[7]uril complex. Toward paramagnetic gyroscopes and rolling nanomachines †

International audienceThe (15-oxo-3,7,11-triazadispiro[5.1.5.3]hexadec-7-yl)oxidanyl, a bis-spiropiperidinium nitroxide derived from TEMPONE, can be included in cucurbit[7]uril to form a strong (K a ∼ 2 × 10 5 M −1) CB[7]@bPTO complex. EPR and MS spectra, DFT calculations, and unparalleled increased resistance (a factor of ∼10 3) toward ascorbic acid reduction show evidence of deep inclusion of bPTO inside CB[7]. The unusual shape of the CB[7]@bPTO EPR spectrum can be explained by an anisotropic Brownian rotational diffusion, the global tumbling of the complex being slower than rotation of bPTO around its " long molecular axis " inside CB[7]. The CB[7] (stator) with the encapsulated bPTO (rotator) behaves as a supramolecular para-magnetic rotor with increased rotational speed of the rotator that has great potential for advanced nano-scale machines requiring wheels such as cucurbiturils with virtually no friction between the wheel and the axle for optimum wheel rotation (i.e. nanopulleys and nanocars)

Effect of MoO3 in the cathode buffer layer on the behaviour of layered organic solar cells

The behaviour of small-molecule organic solar cells based on coper-phthalocyanine/fullerene with different cathode buffer layer is investigated as a function of air exposure duration. We present the study of the effect of MoO3 on the properties of photovoltaic solar cells (OPVCs) when it is introduced in the cathode buffer layer (CBL). Photovoltaic performances were measured as a function of time of air exposure. During the first days of air exposure the efficiency of the OPVCs with MoO3 in their CBL increases significantly, while it decreases immediately after air exposure in the case of reference OPVCs, i.e. without MoO3 in the CBL. Nevertheless, the lifetime of the OPVCs with MoO3 in their CBL is around 60 days, while it is only 10 days in the case of reference OPVCs. The initial increase of the OPVC with MoO3 in their CBL is attributed to the slow decrease of the work function of MoO3 due to progressive contamination. Then, the progressive degradation of the OPVCs efficiency is due water vapour and oxygen contamination of the organic layers. The use of a double CBL, Alq3/MoO3, allows to interrupt the growth of pinholes, defects and increases the path of permeating gas. Also it can prevent the contamination of the organic layer by Al. All this results in significant increase of the lifetime of the OPVCs

Optically Enhanced Solid-State ¹H NMR Spectroscopy

International audienceLow sensitivity is the primary limitation toextending nuclear magnetic resonance (NMR) techniques tomore advanced chemical and structural studies. Photochemicallyinduced dynamic nuclear polarization (photo-CIDNP) is an NMRhyperpolarization technique where light is used to excite a suitabledonor−acceptor system, creating a spin-correlated radical pairwhose evolution drives nuclear hyperpolarization. Systems thatexhibit photo-CIDNP in solids are not common, and this effecthas, up to now, only been observed for 13C and 15N nuclei.However, the low gyromagnetic ratio and natural abundance ofthese nuclei trap the local hyperpolarization in the vicinity of thechromophore and limit the utility for bulk hyperpolarization. Here,we report the first example of optically enhanced solid-state 1HNMR spectroscopy in the high-field regime. This is achieved viaphoto-CIDNP of a donor−chromophore−acceptor molecule in a frozen solution at 0.3 T and 85 K, where spontaneous spindiffusion among the abundant strongly coupled 1H nuclei relays polarization through the whole sample, yielding a 16-fold bulk 1Hsignal enhancement under continuous laser irradiation at 450 nm. These findings enable a new strategy for hyperpolarized NMRbeyond the current limits of conventional microwave-driven DNP

Solid-State NMR/Dynamic Nuclear Polarization of Polypeptides in Planar Supported Lipid Bilayers

Dynamic nuclear polarization has been developed to overcome the limitations of the inherently low signal intensity of NMR spectroscopy. This technique promises to be particularly useful for solid-state NMR spectroscopy where the signals are broadened over a larger frequency range and most investigations rely on recording low gamma nuclei. To extend the range of possible investigations, a triple-resonance flat-coil solid-state NMR probe is presented with microwave irradiation capacities allowing the investigation of static samples at temperatures of 100 K, including supported lipid bilayers. The probe performance allows for two-dimensional separated local field experiments with high-power Lee-Goldberg decoupling and cross-polarization under simultaneous irradiation from a gyrotron microwave generator. Efficient cooling of the sample turned out to be essential for best enhancements and line shape and necessitated the development of a dedicated cooling chamber. Furthermore, a new membrane-anchored biradical is presented, and the geometry of supported membranes was optimized not only for good membrane alignment, handling, stability, and filling factor of the coil but also for heat and microwave dissipation. Enhancement factors of 17-fold were obtained, and a two-dimensional PISEMA spectrum of a transmembrane helical peptide was obtained in less than 2 h

Dynamic Nuclear Polarization NMR Spectroscopy Allows High-Throughput Characterization of Microporous Organic Polymers

Dynamic nuclear polarization (DNP) solid-state NMR was used to obtain natural abundance 13C and 15N CP MAS NMR spectra of microporous organic polymers with excellent signal-to-noise ratio, allowing for unprecedented details in the molecular structure to be determined for these complex polymer networks. Sensitivity enhancements larger than 10 were obtained with bis-nitroxide radical at 14.1 T and low temperature (∼105 K). This DNP MAS NMR approach allows efficient, high-throughput characterization of libraries of porous polymers prepared by combinatorial chemistry methods