Non-thermal plasma abatement of trichloroethylene with DC corona discharges

The decomposition of trichloroethylene (TCE) in air by non-thermal plasma was investigated with a multi-pin-to-plate direct current (DC) discharge at atmospheric pressure and room temperature. The effects of various operating parameters on the removal efficiency (RE) were examined. The experiments indicated that for low energy densities higher removal could be obtained with positive corona. For negative corona and 10 % relative humidity (RH) a maximum RE of 99.5 % could be achieved at 1100 J L-1. Formation of by-products was qualitatively analyzed in detail with FT-IR spectroscopy and mass spectrometry. Detected by-products for negative corona operated at 300 J L-1 and 10 % RH include dichloroacetylchloride, trichloroacetaldehyde, phosgene, ozone, HCl, Cl2, CO and CO2. The highest RE for TCE was achieved with a relative humidity of 19 %

XPF-Dependent DNA Breaks and RNA Polymerase II Arrest Induced by Antitumor DNA Interstrand Crosslinking-Mimetic Alkaloids

SummaryTrabectedin and Zalypsis are two potent anticancer tetrahydroisoquinoline alkaloids that can form a covalent bond with the amino group of a guanine in selected triplets of DNA duplexes and eventually give rise to double-strand breaks. Using well-defined in vitro and in vivo assays, we show that the resulting DNA adducts stimulate, in a concentration-dependent manner, cleavage by the XPF/ERCC1 nuclease on the strand opposite to that bonded by the drug. They also inhibit RNA synthesis by: (1) preventing binding of transcription factors like Sp1 to DNA, and (2) arresting elongating RNA polymerase II at the same nucleotide position regardless of the strand they are located on. Structural models provide a rationale for these findings and highlight the similarity between this type of DNA modification and an interstrand crosslink

Characterization of new Co and Ru on WC catalysts for Fischer-Tropsch reaction. Influence of the carbide surface state.

International audienceAn investigation of the performances in Fischer-Tropsch reaction of 1 wt% M/WC(X) (M = Co, Ru; X=A, B), where A is a tungsten carbide protected by free carbon and B is a clean tungsten carbide, was carried out. Supported catalysts performances were compared to those of the parent tungsten carbides at 473K and 20 bar. It was found that WC(A) produces mainly hydrocarbons but also 20–40% alcohols, whereas WC(B) activity is only towards linear alkanes. Before catalytic test, a reduction in pure hydrogen allows obtaining Co0 and Ru0 dispersed on layers of free carbon covering the WC core for the WC(A), and on a surface free of oxygen for WC(B). Co as Ru dispersions are improved on WC(B) compared to WC(A). A direct consequence is that Co/WC(B) has a better activity than Co/WC(A). Ru–W alloy formation could be responsible of the inobservance of a better activity for Ru/WC(B). On contrary, addition of Ru on WC(A) highly increases the activity and the production of heavy hydrocarbons. This beneficial effect, not observed with cobalt, could be attributed to a better dispersion of ruthenium on a carbon polymeric surface of WC

Study of cobalt and ruthenium supported on WC catalysts for FT reaction.

An investigation of bulk and cobalt or ruthenium supported tungsten carbide was carried out for their use in the Fischer-Tropsch reaction. Two types of WC were studied : tungsten carbide protected by free carbon and clean tungsten carbide, respectively noticed WC(A) and WC(B). XPS analysis shows that after air exposure, the WC(A) carbide surface is protected from the excess carbon whereas a surface W6+ phase is induced during the passivation step for WC(B). However WC(A) is inert towards aqueous impregnation, whereas WC(B) starts to corrode. A reduction in hydrogen at 673 K for Ru and 773K for Co supported catalysts allows obtaining Co0 and Ru0 dispersed on layers of free carbon covering the WC core for WC(A) and on a surface free of oxygen for WC(B). All the catalysts were active for the FT reaction. WC(A) produces mainly light alkanes (78%) and alcohols (22%), whereas no alcohol production is observed for WC(B). Co/WC(B) has a better activity than Co/WC(A), due to a better dispersion of cobalt on WC(B). The addition of Ru on WC(A) allow to obtain an high active catalyst with production of heavy hydrocarbons. On the contrary, formation of a Ru-W alloy could be consider to explain the low activity of Ru/WC(B) catalyst

Epidemiology and clinical features of gastroenteritis in hospitalised children: prospective survey during a 2-year period in a Parisian hospital, France

International audienceRotavirus is recognised as the most important agent of severe acute gastroenteritis (AGE) in young children. In a 2-year prospective survey, we investigated the epidemiology and clinical features of the viral and bacterial pathogens in children hospitalised for AGE. The study was performed in a Parisian teaching hospital from November 2001 to May 2004. Clinical data were prospectively collected to assess the gastroenteritis severity (20-point Vesikari severity score, the need for intravenous rehydration, duration of hospitalisation). Stools were systematically tested for group A rotavirus, norovirus, astrovirus and adenovirus 40/41, sapovirus and Aichi virus and enteropathogenic bacteria. A total of 457 children (mean age 15.9 months) were enrolled. Viruses were detected in 305 cases (66.7%) and bacteria in 31 cases (6.8%). Rotaviruses were the most frequent pathogen (48.8%), followed by noroviruses (8.3%) and adenoviruses, astroviruses, Aichi viruses and sapoviruses in 3.5%, 1.5%, 0.9% and 0.4%, respectively. Cases of rotavirus gastroenteritis were significantly more severe than those of norovirus with respect to the Vesikari score, duration of hospitalisation and the need for intravenous rehydration. Rotaviruses were the most frequent and most severe cause in children hospitalised for AGE, and noroviruses also account for a large number of cases in this population

Oscillatory behavior of Pd-Au catalysts in toluene total oxidation

In this work, the activity of bimetallic Pd-Au doped hierarchically structured titania catalysts has been investigated in the total oxidation of toluene. In earlier works, doping titania with group Vb metal oxides ensured an increased catalytic performance in the elimination of VOC molecules. A synergy between gold and palladium loaded at the surface of titania supports provided better performances in VOC oxidation reactions. Therefore, the main focus in this work was to investigate the durability of the prepared catalysts under long time-on-stream periods. Vanadium-doped catalysts showed a stable activity throughout the whole 110 h test, whereas, surprisingly, niobium-doped catalysts presented a cycle-like activity while nevertheless maintaining a high performance in toluene elimination. Operando Diffuse Reflectance Infrared Fourrier Transform spectroscopy (DRIFT) experiments revealed that variations in the presence of OH radicals and the presence of carbonaceous compounds adsorbed at the surface of spent catalysts varies with the occurrence of oscillations. X-ray Photoelectron Spectroscopy (XPS) results show that interactions between the material and the active phase provided extra amounts of mobile oxygen species and participated in easing the reduction of palladium. An enhanced redox reaction scheme is thus obtained and allows the occurrence of the cyclic-like performance of the catalyst

Temperature-induced melting of double-stranded DNA in the absence and presence of covalently bonded antitumour drugs: insight from molecular dynamics simulations

The difference in melting temperature of a double-stranded (ds) DNA molecule in the absence and presence of bound ligands can provide experimental information about the stabilization brought about by ligand binding. By simulating the dynamic behaviour of a duplex of sequence 5′-d(TAATAACGGATTATT)·5′-d(AATAATCCGTTATTA) in 0.1 M NaCl aqueous solution at 400 K, we have characterized in atomic detail its complete thermal denaturation profile in <200 ns. A striking asymmetry was observed on both sides of the central CGG triplet and the strand separation process was shown to be strongly affected by bonding in the minor groove of the prototypical interstrand crosslinker mitomycin C or the monofunctional tetrahydroisoquinolines trabectedin (Yondelis®), Zalypsis® and PM01183®. Progressive helix unzipping was clearly interspersed with some reannealing events, which were most noticeable in the oligonucleotides containing the monoadducts, which maintained an average of 6 bp in the central region at the end of the simulations. These significant differences attest to the demonstrated ability of these drugs to stabilize dsDNA, stall replication and transcription forks, and recruit DNA repair proteins. This stabilization, quantified here in terms of undisrupted base pairs, supports the view that these monoadducts can functionally mimic a DNA interstrand crosslink

Hydroxyapatite as an unconventional support material : new opportunity for the design of efficient VOC oxidation catalysts

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