529 research outputs found

    Penetration of cefuroxime into the cerebrospinal fluid of patients with traumatic brain injury

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    Cefuroxime levels were measured in cerebrospinal fluid (CSF) and serum of four patients with traumatic brain injury following the implantation of intraventricular catheters. The levels ranged from 0.15 to 2.03 μg/mL in CSF and from 1.8 to 66.9 μg/mL in serum. No ventriculostomy related infections were detecte

    XML Reconstruction View Selection in XML Databases: Complexity Analysis and Approximation Scheme

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    Query evaluation in an XML database requires reconstructing XML subtrees rooted at nodes found by an XML query. Since XML subtree reconstruction can be expensive, one approach to improve query response time is to use reconstruction views - materialized XML subtrees of an XML document, whose nodes are frequently accessed by XML queries. For this approach to be efficient, the principal requirement is a framework for view selection. In this work, we are the first to formalize and study the problem of XML reconstruction view selection. The input is a tree TT, in which every node ii has a size cic_i and profit pip_i, and the size limitation CC. The target is to find a subset of subtrees rooted at nodes i1,⋯ ,iki_1,\cdots, i_k respectively such that ci1+⋯+cik≤Cc_{i_1}+\cdots +c_{i_k}\le C, and pi1+⋯+pikp_{i_1}+\cdots +p_{i_k} is maximal. Furthermore, there is no overlap between any two subtrees selected in the solution. We prove that this problem is NP-hard and present a fully polynomial-time approximation scheme (FPTAS) as a solution

    Following carbon condensation by in-situ TEM : towards a rational understanding of the processes in the synthesis of nitrogen-doped carbonaceous materials.

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    Porous carbonaceous materials obtained from biomass have been an important class of CO2 sorbents since ancient times. Recent progress in carbon-based adsorbent technology is based on the implication of the concept of heteroatom doping. In this respect, the synthesis of carbonaceous materials through one-step condensation of cheap nitrogen-containing molecular precursors is an attractive strategy for obtaining such N-doped carbons. The design of the adsorbents obtained by this route relies on the careful adjustment of synthesis parameters, such as the temperature, the heating rate, and the atmosphere. However, in most cases, the latter's choice remains rather empirical due to the lack of a fundamental understanding of the condensation mechanism of molecular precursors. In this work, we followed the structural, morphological, and chemical evolution of a molecular precursor (uric acid) at the nanoscale using a combination of in-situ condensation inside a scanning transmission electron microscope with ex-situ analysis of the products of condensation at different temperatures, atmospheres, and heating rates, and correlate our findings with the CO2 sorption properties of the obtained materials. We showed that varying pressures and reaction rates result in particles with different porosity. The porosity of the surface of the particles during the early stages of condensation governs the subsequent release of volatiles and the development of a hierarchical pore structure. We found that synthesis in vacuum enables effective condensation at considerably low temperatures (500 °C). Using a higher heating rate (10 °C/min) suppresses structural ripening and preserves the optimal size of micropores, thus giving a CO2 uptake twice as high compared to samples synthesized in nitrogen atmosphere, which is commonly used, preserving the same selectivity.ER

    Cu<sup>II</sup>/Cu<sup>I</sup> decorated N-doped carbonaceous electrocatalysts for the oxygen reduction reaction

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    The oxygen reduction reaction (ORR) that for instance takes place at the cathode of fuel cells is one of the most examined model reactions of energy conversion. The ORR presents sluggish reaction kinetics, thus limiting the overall efficiency of these cells. Pt-based catalysts are still the widest choice though they exhibit important drawbacks such as long-term instability and intolerance to methanol crossover. In this context, engineering transition metals in the form of nano- and subnano-sites on carbonaceous supports has the potential of becoming an alternative to scarce noble metal-based catalysts. Herein, we describe a simple synthetic route towards CuII/CuI decorated N-doped carbonaceous ORR electrocatalysts. CuII/CuI nanosites are obtained by calcination in air of an ionic liquid derived noble carbonaceous support impregnated with copper(ii) acetate. The strong interaction between the copper and the noble support foster the co-formation of CuII/CuI nanosites. Larger amounts of copper(ii) acetate translate into larger amounts of CuI and lower Tafel slopes. The material with 4 wt% of copper catalyzes the selective reduction of oxygen through a 4-electron transfer pathway and exhibits a lower Tafel slope than commercial platinum, a minimal overpotential, and a higher limiting current density. Moreover, all materials show promising durability and high methanol stability, which makes them promising to replace noble metals for the ORR
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