Complete Oxidation (complete + oxidation)

Distribution by Scientific Domains


Selected Abstracts


Ultralow Dielectric Constant Tetravinyltetramethylcyclotetrasiloxane Films Deposited by Initiated Chemical Vapor Deposition (iCVD)

ADVANCED FUNCTIONAL MATERIALS, Issue 4 2010
Nathan J. Trujillo
Abstract Simultaneous improvement of mechanical properties and lowering of the dielectric constant occur when films grown from the cyclic monomer tetravinyltetramethylcyclotetrasiloxane (V4D4) via initiated chemical vapor deposition (iCVD) are thermally cured in air. Clear signatures from silsesquioxane cage structures in the annealed films appear in the Fourier transform IR (1140,cm,1) and Raman (1117,cm,1) spectra. The iCVD method consumes an order of magnitude lower power density than the traditional plasma-enhanced CVD, thus preserving the precursor's delicate ring structure and organic substituents in the as-deposited films. The high degree of structural retention in the as-deposited film allows for the beneficial formation of intrinsically porous silsesquioxane cages upon annealing in air. Complete oxidation of the silicon creates ,Q' groups, which impart greater hardness and modulus to the films by increasing the average connectivity number of the film matrix beyond the percolation of rigidity. The removal of labile hydrocarbon moieties allows for the oxidation of the as-deposited film while simultaneously inducing porosity. This combination of events avoids the typical trade-off between improved mechanical properties and higher dielectric constants. Films annealed at 410,°C have a dielectric constant of 2.15, and a hardness and modulus of 0.78 and 5.4,GPa, respectively. The solvent-less and low-energy nature of iCVD make it attractive from an environmental safety and health perspective. [source]


Genome sequence of Desulfobacterium autotrophicum HRM2, a marine sulfate reducer oxidizing organic carbon completely to carbon dioxide

ENVIRONMENTAL MICROBIOLOGY, Issue 5 2009
Axel W. Strittmatter
Summary Sulfate-reducing bacteria (SRB) belonging to the metabolically versatile Desulfobacteriaceae are abundant in marine sediments and contribute to the global carbon cycle by complete oxidation of organic compounds. Desulfobacterium autotrophicum HRM2 is the first member of this ecophysiologically important group with a now available genome sequence. With 5.6 megabasepairs (Mbp) the genome of Db. autotrophicum HRM2 is about 2 Mbp larger than the sequenced genomes of other sulfate reducers (SRB). A high number of genome plasticity elements (> 100 transposon-related genes), several regions of GC discontinuity and a high number of repetitive elements (132 paralogous genes Mbp,1) point to a different genome evolution when comparing with Desulfovibrio spp. The metabolic versatility of Db. autotrophicum HRM2 is reflected in the presence of genes for the degradation of a variety of organic compounds including long-chain fatty acids and for the Wood,Ljungdahl pathway, which enables the organism to completely oxidize acetyl-CoA to CO2 but also to grow chemolithoautotrophically. The presence of more than 250 proteins of the sensory/regulatory protein families should enable Db. autotrophicum HRM2 to efficiently adapt to changing environmental conditions. Genes encoding periplasmic or cytoplasmic hydrogenases and formate dehydrogenases have been detected as well as genes for the transmembrane TpII- c3, Hme and Rnf complexes. Genes for subunits A, B, C and D as well as for the proposed novel subunits L and F of the heterodisulfide reductases are present. This enzyme is involved in energy conservation in methanoarchaea and it is speculated that it exhibits a similar function in the process of dissimilatory sulfate reduction in Db. autotrophicum HRM2. [source]


Anaerobic degradation of benzene by a marine sulfate-reducing enrichment culture, and cell hybridization of the dominant phylotype

ENVIRONMENTAL MICROBIOLOGY, Issue 1 2008
Florin Musat
Summary The anaerobic biodegradation of benzene, a common constituent of petroleum and one of the least reactive aromatic hydrocarbons, is insufficiently understood with respect to the involved microorganisms and their metabolism. To study these aspects, sulfate-reducing bacteria were enriched with benzene as sole organic substrate using marine sediment as inoculum. Repeated subcultivation yielded a sediment-free enrichment culture constituted of mostly oval-shaped cells and showing benzene-dependent sulfate reduction and growth under strictly anoxic conditions. Amplification and sequencing of 16S rRNA genes from progressively diluted culture samples revealed an abundant phylotype; this was closely related to a clade of Deltaproteobacteria that includes sulfate-reducing bacteria able to degrade naphthalene or other aromatic hydrocarbons. Cell hybridization with two specifically designed 16S rRNA-targeted fluorescent oligonucleotide probes showed that the retrieved phylotype accounted for more than 85% of the cells detectable via DAPI staining (general cell staining) in the enrichment culture. The result suggests that the detected dominant phylotype is the ,candidate species' responsible for the anaerobic degradation of benzene. Quantitative growth experiments revealed complete oxidation of benzene with stoichiometric coupling to the reduction of sulfate to sulfide. Suspensions of benzene-grown cells did not show metabolic activity towards phenol or toluene. This observation suggests that benzene degradation by the enriched sulfate-reducing bacteria does not proceed via anaerobic hydroxylation (mediated through dehydrogenation) to free phenol or methylation to toluene, respectively, which are formerly proposed alternative mechanisms for benzene activation. [source]


Fate of air toxics and VOCs in the odor control scrubbers at the deer island treatment plant

ENVIRONMENTAL PROGRESS & SUSTAINABLE ENERGY, Issue 4 2000
Thomas Myslinski
Process off-gases at the Deer Island wastewater treatment plant in Boston are collected and treated and its stack emissions regulated for selected gases including volatile organic compounds (VOCs), which are monitored as nonmethane hydrocarbons (NMHC). The air treatment processes of countercurrent wet oxidation scrubbing and granulated activated carbon adsorption are available for emissions control at Deer Island. In addition, since the wastewater treatment process of biochemical oxidation is fully enclosed at the site, microbial destruction of VOCs is an intrinsic treatment process for organic gases. Surveyed results of wastewater research literature indicate that the use of scrubbers for the removal of VOCs is controversial, as the fate of volatile hydrocarbon molecules across odor control scrubbers is complex and not fully understood. Continuous emission monitoring tests across the Deer Island scrubbers have consistently shown a VOC removal efficiency in excess of 50%. The fate of the scrubber inlet VOCs at Deer Island was researched as part of a plant-wide, on-going VOC study. Removal efficiencies across the pure oxygen bioreactors were also investigated. Preliminary results of this study indicate chemical reactions involving VOCs in odor control scrubbers partially oxidize and chlorinate derivatives possibly destroying a fraction of the compounds by complete oxidation. In addition, VOC reduction across the enclosed aerobic bioreactors was found to be significant. This article represents the opinions and(legal) conclusions of the authors and not necessarily those of the MWRA. [source]


Redox Cycling of Ni-Based Solid Oxide Fuel Cell Anodes: A Review

FUEL CELLS, Issue 3 2007
D. Sarantaridis
Abstract The published literature relating to damage to SOFCs caused by redox cycling of Ni-based anodes is reviewed. The review covers the kinetics of Ni oxidation and NiO reduction (as single phases and as constituents of composites with yttria-stabilised zirconia, YSZ), the dimensional changes associated with redox cycling and the effect of this on the mechanical integrity and electrical performance of cells and stacks. A critical parameter is the expansion strain that is caused by oxidation. Several studies report that the first complete oxidation of a Ni/YSZ composite causes a linear expansion of the order of 1%, but the actual values vary substantially between different investigations. The oxidation strain is the result of microstructural irreversibility during the redox process and leads to strain accumulation over several redox cycles. This can cause mechanical disruption to an anode, anode support or other cell components attached to the anode. A simplified mechanical model of the stress and damage that are likely to be caused by anode expansion is proposed and applied to anode-supported, electrolyte-supported and inert substrate-supported cell configurations. This allows the maximum oxidation strain to avoid damage in each configuration to be estimated. [source]


Modeling of the catalytic removal of CO and NO in dry combustion gases

AICHE JOURNAL, Issue 3 2010
C. Treviño
Abstract Catalytic removal of pollutants in dry combustion gases in a planar stagnation-point flow over a platinum foil is studied using both numerical and analytical tools. The governing equations have been numerically integrated with the Newton technique, and the response curve has been obtained as functions of temperature and the mixture concentrations. Using the appropriate stoichiometry, the additional oxygen needed to reduce the NO and to achieve complete oxidation of CO has been obtained. The asymptotic analysis leads to an algebraic equation for the surface coverage of empty sites as a function of two nondimensional parameters: the mass transfer number, relating the residence time to the chemical time (sort of Damköhler number), and a parameter, which relates the desorption rate to the adsorption rate of carbon monoxide and depends strongly on temperature. Critical conditions of ignition (light-off) and extinction are identified and closed form solutions are obtained for these phenomena. © 2009 American Institute of Chemical Engineers AIChE J, 2010 [source]


Xylitol Production from Sugarcane Bagasse Hydrolyzate in Fluidized Bed Reactor.

BIOTECHNOLOGY PROGRESS, Issue 4 2003
Effect of Air Flowrate
Cells of Candida guilliermondiiimmobilized onto porous glass spheres were cultured batchwise in a fluidized bed bioreactor for xylitol production from sugarcane bagasse hemicellulose hydrolyzate. An aeration rate of only 25 mL/min ensured minimum yields of xylose consumption (0.60) and biomass production (0.14 gDM/gXyl), as well as maximum xylitol yield (0.54 gXyt/gXyl) and ratio of immobilized to total cells (0.83). These results suggest that cell metabolism, although slow because of oxygen limitation, was mainly addressed to xylitol production. A progressive increase in the aeration rate up to 140 mL/min accelerated both xylose consumption (from 0.36 to 0.78 gXyl/L·h) and xylitol formation (from 0.19 to 0.28 gXyt/L·h) but caused the fraction of immobilized to total cells and the xylitol yield to decrease up to 0.22 and 0.36 gXyt/gXyl, respectively. The highest xylitol concentration (17.0 gXyt/L) was obtained at 70 mL/min, but the specific xylitol productivity and the xylitol yield were 43% and 22% lower than the corresponding values obtained at the lowest air flowrate, respectively. The concentrations of consumed substrates and formed products were used in material balances to evaluate the xylose fractions consumed by C. guilliermondii for xylitol production, complete oxidation through the hexose monophosphate shunt, and cell growth. The experimental data collected at variable oxygen level allowed estimating a P/O ratio of 1.35 molATP/molO and overall ATP requirements for biomass growth and maintenance of 3.4 molATP/C-molDM. [source]