Academic literature on the topic 'No-Co/ftir'

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Journal articles on the topic "No-Co/ftir"

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Ivanova, Elena, Mihail Mihaylov, Frédéric Thibault-Starzyk, Marco Daturi, and Konstantin Hadjiivanov. "FTIR spectroscopy study of CO and NO adsorption and co-adsorption on Pt/TiO2." Journal of Molecular Catalysis A: Chemical 274, no. 1-2 (2007): 179–84. http://dx.doi.org/10.1016/j.molcata.2007.05.006.

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Zdravkova, Videlina, Nikola Drenchev, Kristina Chakarova, Mihail Mihaylov, and Konstantin Hadjiivanov. "FTIR Study of CO and NO Coadsorption on Cu-ZSM-5: Does a Cu+(CO)(NO) Complex Exist?" Current Physical Chemistry 6, no. 2 (2016): 152–61. http://dx.doi.org/10.2174/1877946806666160120221645.

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Penkova, A., and K. Hadjiivanov. "FTIR spectroscopic study of CO and NO adsorption on Cr-ZSM-5." Catalysis Communications 4, no. 9 (2003): 485–91. http://dx.doi.org/10.1016/s1566-7367(03)00129-8.

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Yang, Shuwu, Yongxue Li, Jiang Xu, et al. "FTIR study of CO and NO adsorbed on nitrided CoMo/Al2O3 catalysts." Physical Chemistry Chemical Physics 2, no. 14 (2000): 3313–17. http://dx.doi.org/10.1039/b002557g.

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Ivanova, Elena, Konstantin Hadjiivanov, Dimitar Klissurski, Maria Bevilacqua, Tiziana Armaroli, and Guido Busca. "FTIR study of species arising after NO adsorption and NO+O2 co-adsorption on CoY: comparison with Co-ZSM-5." Microporous and Mesoporous Materials 46, no. 2-3 (2001): 299–309. http://dx.doi.org/10.1016/s1387-1811(01)00311-0.

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Hadjiivanov, Konstantin, and Helmut Knözinger. "Species formed after NO adsorption and NO + O2 co-adsorption on TiO2: an FTIR spectroscopic study." Physical Chemistry Chemical Physics 2, no. 12 (2000): 2803–6. http://dx.doi.org/10.1039/b002065f.

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Frache, Alberto, Marcella Cadoni, Chiara Bisio, Leonardo Marchese, Artur J. S. Mascarenhas, and Heloise O. Pastore. "NO and CO Adsorption on Over-Exchanged Cu-MCM-22: A FTIR Study." Langmuir 18, no. 18 (2002): 6875–80. http://dx.doi.org/10.1021/la0257081.

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Raskó, J., Z. Szabó, T. Bánsági, and F. Solymosi. "FTIR study of the photo-induced reaction of NO+CO on Rh/TiO2." Physical Chemistry Chemical Physics 3, no. 19 (2001): 4437–43. http://dx.doi.org/10.1039/b103627k.

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Chenier, J. H. B., J. A. Howard, H. A. Joly, B. Mile, and M. Tomietto. "A spectroscopic study of the reaction of gold atoms with CO in a rotating cryostat: formation of a variety of gold carbonyls." Canadian Journal of Chemistry 67, no. 4 (1989): 655–61. http://dx.doi.org/10.1139/v89-099.

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Reaction of 197Au atoms with CO has been studied in inert hydrocarbon matrices in a rotating cryostat at 77 K by EPR, FTIR, and UV/visible spectroscopy. Au(CO)2 has been positively identified by FTIR spectroscopy and there is evidence for the formation of AuCO, a gold microcrystallite – CO complex and, upon annealing, Au2(CO)4. Electron paramagnetic resonance spectra are consistent with the formation of Au(CO) (OC) with the magnetic parameters: a13 = 325 MHz, a17 = 44 MHz, and g = 2.0014 and a gold microcrystallite – CO complex with g = 2.014. An intense broad absorption in the optical spectru
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Jang, H. J., W. Keith Hall, and Julie L. d'Itri. "Redox Behavior of CuZSM-5 Catalysts: FTIR Investigations of Reactions of Adsorbed NO and CO." Journal of Physical Chemistry 100, no. 22 (1996): 9416–20. http://dx.doi.org/10.1021/jp952525x.

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Dissertations / Theses on the topic "No-Co/ftir"

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Hérault, Nelly. "Préparation contrôlée de catalyseurs bimétalliques Pt-Rh supportés." Thesis, Poitiers, 2014. http://www.theses.fr/2014POIT2298/document.

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Les catalyseurs Pt-Rh supportés ont montré des propriétés intéressantes en ouverture sélective des naphtènes. Les performances catalytiques de ces catalyseurs dépendent, entre autres, de l'interaction entre le rhodium et le platine. L'objectif de ces travaux portait sur l'étude de l'influence de la méthode de préparation sur les interactions Pt-Rh. Dans ce but, plusieurs voies reposant sur des stratégies de synthèse différentes ont été sélectionnées, des plus classiques, comme l'imprégnation, aux plus sophistiquées, comme la modification d'un catalyseur monométallique parent par ajout d'un sec
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Book chapters on the topic "No-Co/ftir"

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Pietrzyk, P., E. Kukulska-Zając, D. Lorens, Z. Sojka, and J. Datka. "The interaction of Co and No with Co sites in CoZSM-5 zeolite. FTIR, EPR and theoretical studies." In Recent Advances in the Science and Technology of Zeolites and Related Materials Part B, Proceedings of the 14th International Zeolite Conference. Elsevier, 2004. http://dx.doi.org/10.1016/s0167-2991(04)80682-7.

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Martins, Ruth Leibsohn, Maria Auxiliadora S. Baldanza, Marcos Teixeira Lima, and Martin Schmal. "Direct FTIR Insight in the Spillover Hydrogen Reactivity: CO and NO Chemisorbed on Ru NaY Zeolite." In Spillover and Mobility of Species on Solid Surfaces. Elsevier, 2001. http://dx.doi.org/10.1016/s0167-2991(01)80042-2.

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"FTIR Remote Sensing of Biomass Burning Emissions of CO2, CO,CH4, CH20, NO, N02, NH3, and N20." In Global Biomass Burning. The MIT Press, 1991. http://dx.doi.org/10.7551/mitpress/3286.003.0034.

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Kuba, Stefan, Konstantin Hadjiivanov, and Helmut Knözinger. "Reactivity of the NO surface species formed after co-adsorption of NOO2 on a WO3/ZrO2 catalyst: An FTIR spectroscopic study." In Studies in Surface Science and Catalysis. Elsevier, 2000. http://dx.doi.org/10.1016/s0167-2991(00)80372-9.

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Zhang, Weigang, Changming Xie, Min Ge, and Xi Wei. "C/C-ZrB2-ZrC-SiC Composites Derived from Polymeric Precursor Infiltration and Pyrolysis Part I." In MAX Phases and Ultra-High Temperature Ceramics for Extreme Environments. IGI Global, 2013. http://dx.doi.org/10.4018/978-1-4666-4066-5.ch013.

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Two-dimensional C/C-ZrB2-ZrC-SiC composites with three phases of ultra high temperature ceramics (UHTCs) are fabricated for the first time using blending pre-ceramic polymeric precursors through the traditional polymer infiltration and pyrolysis (PIP) technique, in which a porous carbon fiber reinforced pyrolytic carbon (C/C) with a porosity of about 60% is prepared as preforms. The fabricated composite possesses a matrix of 20ZrB2-30ZrC-50SiC, which is obtained by co-pyrolysis of three pre-ceramic polymers solution in xylene with certain molar ratios. Pyrolysis of these ZrB2-ZrC-SiC pre-ceramic precursors is studied with XRD characterization of the residual solids. The gas phase products are analysized with an on-line GC-MS-FTIR coupling technique, which confirms the formation of crystalline ZrC and ZrB2 from these precursors at temperatures above 1400°C. Possible mechanisms of pyrolysis and formation of pure ZrB2 from the precursors with various B/Zr molar ratios are suggested. The densification process and microstructures of the fabricated composite are studied. It is found that a composite with a bulk density of 2.06 g/cm3 and open porosity of 9.6% can be obtained after 16 PIP cycles. The formed matrix exhibits homogeneous dispersion of three matrix ceramics without any oxide impurities, i.e., the nano sized ZrB2 and ZrC particles dispersed in a continuous SiC ceramic with clean crystalline boundaries and particle dimensions less than 200 nm. No erosion or interface reaction occurs upon the carbon fiber reinforcement, which therefore avoids a dramatic deterioration of mechanical strength of carbon fiber and the composite. Improvement of PIP benefits from two aspects; firstly, the dense pyrolytic carbon interphase deposited on fiber surface by CVI serves as barrier coating and secondly, pyrolysis of the novel organic polymeric precursors does not release corrosive by-products such as hydrogen chloride.
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Conference papers on the topic "No-Co/ftir"

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Aldina, G. J., and Jeffrey L. Hahn. "Validation Study of FTIR-Based Emissions Measurements at a Municipal Waste Combustor." In 13th Annual North American Waste-to-Energy Conference. ASMEDC, 2005. http://dx.doi.org/10.1115/nawtec13-3158.

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EPA Test Methods 301 and 320 include statistical techniques for validating sampling methods in specific gas matrices. Several of these techniques were used to analyze extractive FTIR data collected at a municipal solid waste incinerator and to validate the method for hydrogen chloride (HCl) measurements. FTIR results for carbon monoxide (CO), sulfur dioxide (SO2), and nitric oxide (NO) were also compared to measurements recorded by the facility’s continuous emissions monitors (CEMs). Presented are discussions of the equipment, spectral analyses, and statistical comparisons of the various test
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Oliver, William, David F. Marran, Martin L. Spartz, John C. Y. Lee, and Waseem Nazeer. "Evaluation of the MKS On-Line FTIR MultiGas™ Analyzer for Gas Turbine Applications." In ASME Turbo Expo 2003, collocated with the 2003 International Joint Power Generation Conference. ASMEDC, 2003. http://dx.doi.org/10.1115/gt2003-38656.

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A side-by-side comparison between the MKS On-Line MultiGas™ analyzer (MGA) and conventional continuous emissions monitoring systems (CEMS) was performed under various test rig operating conditions at Solar Turbines Incorporated (Solar). The CEMS used an array of single gas analyzers (SGA’s) to measure NOX, CO, CO2, O2 and UHC (unburned hydrocarbons). The MGA, which uses Fourier transform infrared (FTIR) spectrometry to make its measurements, simultaneously analyzed the exhaust stream for ten compounds: NO, NO2, CO, CO2, H2O, CH4, H2CO (formaldehyde), N2O, SO2, and NH3. Both dry and wet samples
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Cordon, Dan, Steve Beyerlein, Judi Steciak, and Karen DenBraven. "Measuring and Comparing Accuracy of Emissions Analyzers for Use With IC Engines." In ASME 2009 International Mechanical Engineering Congress and Exposition. ASMEDC, 2009. http://dx.doi.org/10.1115/imece2009-11295.

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Automotive emission analyzers vary in price from under $1000 to well over $100,000. Different analyzers use various technologies to detect exhaust concentrations, and differ in how they condition the sample — leading to a difference in price and performance. Manufacturer claims on accuracy from less expensive analyzers are often similar to much more expensive analyzers. With a variety of analyzers available in the Small Engine Research Facility (SmERF) at the University of Idaho, this often leads to confusion in reporting accuracy of exhaust gas measurements. This study benchmarks the performa
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Miller, M. N., C. W. Wilson, M. Hilton, and G. Marston. "Quantitative Determination of Methane, Ethene, Ethyne, and Benzene From Within the Sector of a Gas Turbine Combustor." In ASME Turbo Expo 2004: Power for Land, Sea, and Air. ASMEDC, 2004. http://dx.doi.org/10.1115/gt2004-53362.

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This paper describes experimental work undertaken in the quantitative measurement of specific hydrocarbons found at different axial locations within a gas turbine combustor. The motivation for this work was to gain a greater understanding of the combustion process and obtain data which could be used to provide validation for computational fluid dynamic and chemical kinetic models. Chemical species routinely measured using the QinetiQ internal traversing facility are: H2, O2, NO, NO2, THC, CO2, CO and smoke. For this work, a Fourier Transform Infrared spectrometer (FTIR) was added to the suite
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Hayashida, Kazuhiro, Kenji Amagai, and Masataka Arai. "Exhaust Gas Analysis in a Catalytic Combustion System With a Methane Mixture." In 2002 International Joint Power Generation Conference. ASMEDC, 2002. http://dx.doi.org/10.1115/ijpgc2002-26133.

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Exhaust gas from the catalytic combustion of methane mixture was analyzed experimentally. A palladium catalyst supported on a cordierite honeycomb was used. The methane/air mixture, which was pre-heated to 530K, was introduced into the catalyst. Combustion states were investigated under various conditions of the equivalence ratio. In the case of lean mixture, homogeneous surface reaction in the catalyst was observed, and combustion reaction was completed within the catalyst. However, in the case of rich mixture, a thermal combustion flame appeared after the catalyst with the homogeneous surfac
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Andrews, Gordon E., Aysha Irshad, Herodotus N. Phylaktou, and Bernard M. Gibbs. "Solid Biomass to Medium CV Gas Conversion With Rich Combustion." In ASME Turbo Expo 2019: Turbomachinery Technical Conference and Exposition. American Society of Mechanical Engineers, 2019. http://dx.doi.org/10.1115/gt2019-90196.

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Abstract A modified cone calorimeter for controlled atmosphere combustion was used to investigate the gases released from fixed bed rich combustion of solid biomass. The cone calorimeter was used with 50 kW/m2 of radiant heat that simulated a larger gasification system. The test specimen in the cone calorimeter is 100mm square and this sits on a load cell so that the mass burn rate can be determined. Pine wood was burned with fixed air ventilation that created rich combustion at 1.5–4 equivalence ratio, Ø. The raw exhaust gas was sampled using a multi-hole gas sample probe in a discharge chimn
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Christensen, Stephen, Kayode Ajayi, Duane Abata, and Kevin Carlin. "An Experimental and Theoretical Study of Fuel Composition on Noxious Emissions in a Natural Gas Engine Operating on Wellhead Gas." In ASME 2015 Internal Combustion Engine Division Fall Technical Conference. American Society of Mechanical Engineers, 2015. http://dx.doi.org/10.1115/icef2015-1050.

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The use of natural gas in spark-ignited internal combustion engines optimized for minimum emissions has repeatedly shown a significant reduction in exhaust emissions over that of gasoline. Pronounced variations in unprocessed natural gas composition can however present an emissions problem for engines used in natural gas recovery where unrefined wellhead gas is used as the fuel. This study is twofold involving both experimental analysis and theoretical development with a computer model that simulates wellhead gas combustion. On the experimental side, Fourier transform infrared spectroscopy (FT
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Soloiu, Valentin, Marvin Duggan, Henry Ochieng, David Williams, Gustavo Molina, and Brian Vlcek. "Investigation of Low Temperature Combustion Regimes of Biodiesel With n-Butanol Injected in the Intake Manifold of a Compression Ignition Engine." In ASME 2012 Internal Combustion Engine Division Fall Technical Conference. American Society of Mechanical Engineers, 2012. http://dx.doi.org/10.1115/icef2012-92053.

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In this study, the in-cylinder soot and NOx trade off was investigated in a Compression Engine by implementing Premixed Charge Compression Ignition (PCCI) coupled with Low Temperature Combustion (LTC) for selected regimes of 1–3 bars IMEP. In order to achieve that, an omnivorous (multi-fuel) single cylinder diesel engine was developed by injecting n-butanol in the intake port while being fueled with biodiesel by direct injection in the combustion chamber. By applying this methodology, the in-cylinder pressure decreased by 25% and peak pressure was delayed in the power stroke by about 8 CAD for
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