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Relevant bibliographies by topics / Kinetics; Oxidation; DMF (N

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Academic literature on the topic 'Kinetics; Oxidation; DMF (N'

Author: Grafiati

Published: 5 June 2025

Last updated: 2 August 2025

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Journal articles on the topic "Kinetics; Oxidation; DMF (N"

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S., Sheik Mansoor, and H. Asghar Basim. "Studies on the kinetics of tetrahexylammonium bromochromate oxidation of methionine in various percentage of acetic acid + N,N-dimethylformamide mixture." Journal of Indian Chemical Society Vol. 90, Sep 2013 (2013): 1395–401. https://doi.org/10.5281/zenodo.5789184.

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Post Graduate and Research Department of Chemistry, C. Abdul Hakeem College, Melvisharam-632 509, Tamilnadu, India <em>E-mail </em>: smansoors2000@yahoo.co.in Department of Chemistry, Faculty of Applied Sciences, Umm Al-Qura University, Makkah, Saudi Arabia <em>Manuscript received online 21 October 2012, revised 18 November 2012, accepted 19 November 2012</em> Abstract : Methionine (Met) is a naturally occurring sulphur containing amino acid. The kinetics of oxidation of methionine by tetrahexylammonium bromochromate (THexABC) in various percentage of acetic acid + <em>N,N</em>-dimethylformami

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Munna, Lal Meena. "A kinetic and mechanistic study of oxidation of N-Acetyl-DL-Methionine by pyridinium chlorochromate in aqueous DMF medium." GSC Advanced Research and Reviews 20, no. 1 (2024): 484–94. https://doi.org/10.5281/zenodo.13685185.

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The Kinetics of Oxidative transformation of N-Acetyl-DL-Methionine by pyridinium chlorochromate in aqueous DMF medium, containing perchloric acid has been studied at 40 ℃. The rate of reaction was found to be of first order dependence on PCC, N-Acetyl-DL-Methionine, and H<sup>+</sup> ion Concentration. Michaelis–Menten type kinetics is observed respect to substrate. The increase in the rate of reaction with increase in acidity indicates the involvement of a protonated chromium(VI) species in the rate-determining step. The product of oxidation has been identified as N-Acetyl-DL-Methionine

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Munna, Lal Meena. "Oxidation of threonine by Corey's reagent: A kinetic study." World Journal of Biology Pharmacy and Health Sciences 18, no. 3 (2024): 395–402. https://doi.org/10.5281/zenodo.13767651.

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Oxidation of Threonine by pyridinium chlorochromate in DMF-water medium has been studied. The rate of reaction was found to be of first order dependence on [PCC], [Threonine] and [H+]. The Michaelis–Menten type kinetics is observed with respect to Threonine. The increase in the rate of oxidation with increase in acidity indicates the involvement of a protonated chromium (VI) species in the rate-determining step. The product of oxidation has been identified as an aldehyde. The rate of reaction decreased with increase in the polarity of medium indicates that there is involvement of an ion-

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Munna, Lal Meena. "Kinetic and mechanistic study of oxidation of valine by pyridinium chlorochromate in aqueous DMF medium." World Journal of Biology Pharmacy and Health Sciences 14, no. 3 (2023): 053–62. https://doi.org/10.5281/zenodo.8285571.

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Oxidative transformation of Valine by pyridinium chlorochromate in aqueous DMF medium, containing perchloric acid has been studied at 40 ℃. The rate of reaction was found to be of first order dependence on Oxidant, Valine, and H<sup>+</sup> ion Concentration. The increase in the rate of reaction with increase in acidity indicates the involvement of a protonated chromium(VI) species in the rate-determining step. The product of oxidation has been identified as aldehyde. The rate of reaction decreased with increase in the polarity (dielectric constant of medium) of solvent, which indicates t

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Munna Lal Meena. "A kinetic and mechanistic study of oxidation of N-Acetyl-DL-Methionine by pyridinium chlorochromate in aqueous DMF medium." GSC Advanced Research and Reviews 20, no. 1 (2024): 484–94. http://dx.doi.org/10.30574/gscarr.2024.20.1.0311.

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The Kinetics of Oxidative transformation of N-Acetyl-DL-Methionine by pyridinium chlorochromate in aqueous DMF medium, containing perchloric acid has been studied at 40 ℃. The rate of reaction was found to be of first order dependence on PCC, N-Acetyl-DL-Methionine, and H+ ion Concentration. Michaelis–Menten type kinetics is observed respect to substrate. The increase in the rate of reaction with increase in acidity indicates the involvement of a protonated chromium(VI) species in the rate-determining step. The product of oxidation has been identified as N-Acetyl-DL-Methionine sulfoxide. The r

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Munna Lal Meena. "A kinetic and mechanistic study of oxidation of N-Acetyl-DL-Methionine by pyridinium chlorochromate in aqueous DMF medium." GSC Advanced Research and Reviews 20, no. 2 (2024): 146–56. http://dx.doi.org/10.30574/gscarr.2024.20.2.0304.

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The Kinetics of Oxidative transformation of N-Acetyl-DL-Methionine by pyridinium chlorochromate in aqueous DMF medium, containing perchloric acid has been studied at 40 ℃. The rate of reaction was found to be of first order dependence on PCC, N-Acetyl-DL-Methionine, and H+ ion Concentration. Michaelis–Menten type kinetics is observed respect to substrate. The increase in the rate of reaction with increase in acidity indicates the involvement of a protonated chromium(VI) species in the rate-determining step. The product of oxidation has been identified as N-Acetyl-DL-Methionine sulfoxide. The r

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Al-Duri, Bushra, Faihan Alsoqyani, and Iain Kings. "Supercritical water oxidation for the destruction of hazardous waste: better than incineration." Philosophical Transactions of the Royal Society A: Mathematical, Physical and Engineering Sciences 373, no. 2057 (2015): 20150013. http://dx.doi.org/10.1098/rsta.2015.0013.

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Supercritical water oxidation (SCWO) is an advanced process mainly employed for the treatment of hazardous stable wastes, otherwise treatable by incineration. It is based on the unique properties of water above its critical point ( T c =675 K, P c =22.2 MPa), making it a superior reaction medium for the destruction of all organics in the presence of oxygen. This work presents preliminary laboratory scale studies on SCWO of nitrogen (N)-containing hazardous hydrocarbons, with a view to enhancing the process performance, using available reagents and non-complex reactor design. This article inves

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Rajarajan, Govindasamy, Natesan Jayachandramani, Subramaniyan Manivarman, Jayaraman Jayabharathi та Venugopal Thanikachalam. "Kinetics and mechanism of oxidation of N,α-diphenylnitrones by 4-(dimethylamino)pyridinium chlorochromate (DMAPCC) in aqueous DMF medium". Transition Metal Chemistry 33, № 3 (2008): 393–97. http://dx.doi.org/10.1007/s11243-008-9055-1.

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Fomenko, Iakov, Artem Gushchin, Pavel Abramov, et al. "New Oxidovanadium(IV) Complexes with 2,2′-bipyridine and 1,10-phenathroline Ligands: Synthesis, Structure and High Catalytic Activity in Oxidations of Alkanes and Alcohols with Peroxides." Catalysts 9, no. 3 (2019): 217. http://dx.doi.org/10.3390/catal9030217.

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Reactions of [VCl3(thf)3] or VBr3 with 2,2′-bipyridine (bpy) or 1,10-phenanthroline (phen) in a 1:1 molar ratio in air under solventothermal conditions has afforded polymeric oxidovanadium(IV) four complexes 1–4 of a general formula [VO(L)X2]n (L = bpy, phen and X = Cl, Br). Monomeric complex [VO(DMF)(phen)Br2] (4a) has been obtained by the treatment of compound 4 with DMF. The complexes were characterized by IR spectroscopy and elemental analysis. The crystal structures of 3 and 4a were determined by an X-ray diffraction (XRD) analysis. The {VOBr2(bpy)} fragments in 3 form infinite chains due

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Barrios-Reyna, M. L., J. Uribe-Godínez, J. M. Olivares-Ramírez, and O. Jiménez-Sandoval. "Study of IrxMny(CO)n(DMF)z as Electrocatalyst for Oxygen Reduction and Hydrogen Oxidation in the Presence of Fuel Cell Contaminants." Journal of New Materials for Electrochemical Systems 19, no. 4 (2016): 185–92. http://dx.doi.org/10.14447/jnmes.v19i4.284.

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The oxygen reduction reaction (ORR) and the hydrogen oxidation reaction (HOR) have been studied on a wide range of elec-trocatalysts, including bimetallic materials which are based solely on platinum group metals and their alloys. This work reports the synthe-sis and characterization of a novel bimetallic electrocatalyst, IrxMny(CO)n(DMF)z, for the ORR and HOR in acid media. The material was synthesized by reacting Ir4(CO)12 and MnCl2·4H2O in DMF. It was characterized structurally by FT-IR and micro-Raman spectroscopy, X-ray diffraction, SEM and energy-dispersive X-ray spectroscopy; the electr

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Dissertations / Theses on the topic "Kinetics; Oxidation; DMF (N"

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Srivastav, Rajat. "Kinetics of NDMA (N-nitrosodimethylamine) oxidation by permanganate under a range of pH and temperature conditions." Connect to online resource, 2008. http://gateway.proquest.com/openurl?url_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:dissertation&res_dat=xri:pqdiss&rft_dat=xri:pqdiss:1460876.

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Zhang, Huichun. "Metal oxide-facilitated oxidation of antibacterial agents." Diss., Available online, Georgia Institute of Technology, 2004:, 2004. http://etd.gatech.edu/theses/available/etd-07072004-152317/unrestricted/zhang%5Fhuichun%5F200407%5Fphd.pdf.

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Thesis (Ph. D.)--School of Civil and Environmental Engineering, Georgia Institute of Technology, 2005. Directed by Ching-Hua Huang.<br>Wine, Paul, Committee Member ; Pavlostathis, Spyros, Committee Member ; Mulholland, James, Committee Member ; Yiacoumi, Sotira, Committee Member ; Huang, Ching-Hua, Committee Chair. Includes bibliographical references.

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Hakka, Mohammed Hichem. "Étude de l'oxydation en phase gazeuse de composants des gazoles et des biocarburants diesel." Thesis, Vandoeuvre-les-Nancy, INPL, 2010. http://www.theses.fr/2010INPL001N/document.

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En raison de la complexité de leur composition, l’étude de l’oxydation des gazoles et des carburants biodiesel nécessite de choisir des molécules modèles représentant ces mélanges. Dans ce contexte nous avons sélectionné deux molécules pouvant représenter les gazoles : le n-décane, souvent considéré comme molécule modèle des paraffines contenues dans les gazoles, et le n-hexadécane, molécule de référence pour l’estimation de l’indice cétane, ainsi que deux molécules représentant les carburants biodiesel : le palmitate de méthyle (C17H34O2, ester méthylique saturé) et l’oléate de méthyle (C19H3

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Mokrani, Nabil. "Effet des paramètres physiques et d’additifs sur l'allumage du n-décane par claquage laser non résonant." Thesis, Orléans, 2016. http://www.theses.fr/2016ORLE2062/document.

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L’allumage par claquage laser non résonant des mélanges réactifs considérés à l’état gazeux et au repos est étudié dans ce travail, principalement avec des mélanges n-décane/air (C₁₀H₂₂+N₂+O₂). Ce système est considéré comme étant prometteur dans les différentes stratégies futures concernant les systèmes d’allumages équipant les moteurs à combustion interne. Le plasma d’allumage est généré en focalisant un faisceau laser de haute intensité pendant quelques nanosecondes. Le laser Nd :YAG opère à 1064 nm, il est choisi comme source laser pour l’ensemble des expériences menées en laboratoire afin

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Fox, Clayton D. L. "Modeling Simplified Reaction Mechanisms using Continuous Thermodynamics for Hydrocarbon Fuels." Thesis, Université d'Ottawa / University of Ottawa, 2018. http://hdl.handle.net/10393/37554.

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Commercial fuels are mixtures with large numbers of components. Continuous thermodynamics is a technique for modelling fuel mixtures using a probability density function rather than dealing with each discreet component. The mean and standard deviation of the distribution are then used to model the chemical reactions of the mixture. This thesis develops the necessary theory to apply the technique of continuous thermodynamics to the oxidation reactions of hydrocarbon fuels. The theory is applied to three simplified models of hydrocarbon oxidation: a global one-step reaction, a two-step reaction

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Huang, Yen-Wei, and 黃彥瑋. "Study on The Regenerative Thermal Oxidation of Gas-borne N,N-dimethylformamide (DMF) and Its Associated NOx Formation Characteristics." Thesis, 2006. http://ndltd.ncl.edu.tw/handle/53822339985911429036.

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碩士<br>國立中山大學<br>環境工程研究所<br>94<br>In this study, a two-bed electrically-heated regenerative thermal oxidizer (RTO) was used to test NOx formation characteristics from burning air-laden N, N-dimethyl formamide (DMF) and air-laden DMF mixed with methyl ethyl ketone (MEK). The RTO contained two 0.152 m × 0.14 m × 1.0 m (L × W × H) beds both packed with gravel particles of around 1.11 cm in average diameter to a height of 1.0 m, and the packed section had a void fraction of 0.416. Performances on the thermal destructions of DMF and MEK, the thermal recovery efficiency, as well as the gas pressure

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Manjunathswamy, H. "Kinetics and Mechanism of Oxidation of some Organic substrates with N-chloro-p-toluenesulphonamide." Thesis, 1998. http://hdl.handle.net/2009/5979.

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Hsu, Hui-Jan, and 許惠然. "The Effect of N/Ti Molar Ratio and Calcination Temperature on the Characteristics of N-Doped TiO2 Catalyst and Kinetics of Heterogeneous Photocatalytic Oxidation of Ethylene." Thesis, 2012. http://ndltd.ncl.edu.tw/handle/08521795081611222414.

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碩士<br>國立中興大學<br>土壤環境科學系所<br>100<br>The conservation deadline of vegetables and fruits are limiting with plants hormone ethylene which always are promoting them ripe. Therefore, we use the photocatalyst of N-doped TiO2 degrade ethylene pollutant under visible light response. It aims that we can remove of ethylene for vegetables and fruits, improving the conservation deadline of vegetables and fruits. In our studies, the titanium tetraisopropoxide and aqua ammonia are titanium and nitrogen precursor, respectively. We had focused on the sol gel synthesis of N-doped TiO2 at calcination temperature

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Rotavera, Brandon Michael. "Oxidation Kinetics of Pure and Blended Methyl Octanoate/n-Nonane/Methylcyclohexane: Measurements and Modeling of OH*/CH* Chemiluminescence, Ignition Delay Times and Laminar Flame Speeds." Thesis, 2012. http://hdl.handle.net/1969.1/ETD-TAMU-2012-05-10959.

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The focus of the present work is on the empirical characterization and modeling of ignition trends of ternary blends of three distinct hydrocarbon classes, namely a methyl ester (C9H18O2), a linear alkane (n-C9H20), and a cycloalkane (MCH). Numerous surrogate biofuel formulations have been proposed in the literature, yet specific blending of these species has not been studied. Moreover, the effects of blending biofuel compounds with conventional hydrocarbons are not widely studied and a further point is the lack of studies paying specific attention to the effects of fuel variation within a giv

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Books on the topic "Kinetics; Oxidation; DMF (N"

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Taufiq-Yap, Y. H. A study of the kinetics and mechanism of the partial oxidation of n-butane anad but-1-ene to maleic anhydride. UMIST, 1997.

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Sanguanruang, Oravan. [Lambda hyperon]-((R)-cysteinesulfenamido-N,S) bis (ethylenediamine) cobalt(III) complex: Characterization of the complex and kinetics and mechanism of formation and base-catalyzed decomposition. 1988.

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Sanguanruang, Oravan. [Lambda hyperon]-((R)-cysteinesulfenamido-N,S) bis (ethylenediamine) cobalt(III) complex: Characterization of the complex and kinetics and mechanism of formation and base-catalyzed decomposition. 1988.

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Book chapters on the topic "Kinetics; Oxidation; DMF (N"

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Sun, S. C., and H. Y. Chang. "Oxidation Simulation and Growth Kinetics of Thin SiO 2 in Pure N 2 O." In Simulation of Semiconductor Devices and Processes. Springer Vienna, 1993. http://dx.doi.org/10.1007/978-3-7091-6657-4_41.

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Anowar Hossain, Md. "Evaluation of Camouflage Coloration of Polyamide-6,6 Fabric by Comparing Simultaneous Spectrum in Visible and Near-Infrared Region for Defense Applications." In Colorimetry [Working Title]. IntechOpen, 2021. http://dx.doi.org/10.5772/intechopen.101537.

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Polyamide-6,6 (PA-6,6) knitted fabric was coated with a complex combination of liquid-phase oxidized carbon black pigment (CBP) as light absorber and mono-sulfonated telon violet 3R (TVR) as acid dyes. Nitric acid (NA) moiety was used as liquid-phase oxidation of CBP and hydrophilic transformation of CBP-TVR. Thermoplastic polyurethane (TPU) and N, N-dimethylformamide (DMF) were formulated as cross-linker between composite mixture (CM) and PA-6,6 fabric. Six different CMs were coded for coating of PA-6, 6 fabric such as TPU-DMF, CBP-TPU-DMF, TVR-TPU-DMF, CBP-TVR-TPU-DMF, NA-TVR-TPU-DMF, NA-CBP

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Madeira, L. M., and M. F. Portela. "Kinetics and mechanism of the selective oxidation and degradation of n-butane over nickel molybdate catalysts." In Natural Gas Conversion V, Proceedings ofthe 5th International Natural Gas Conversion Symposium,. Elsevier, 1998. http://dx.doi.org/10.1016/s0167-2991(98)80499-0.

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Dowell, D., J. T. Gleaves, and Y. Schuurman. "The nature of the active/selective phase in VPO catalysts and the kinetics of n-butane oxidation." In Studies in Surface Science and Catalysis. Elsevier, 1997. http://dx.doi.org/10.1016/s0167-2991(97)80980-9.

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O’Connor, Ryan P., and Lanny D. Schmidt. "Oxygenates and Olefins from Catalytic Partial Oxidation of Cyclohexane and n-Hexane in Single-Gauze Chemical Reactors." In Reaction Kinetics and the Development and Operation of Catalytic Processes, Proceedings of the 3rd International Symposium. Elsevier, 2001. http://dx.doi.org/10.1016/s0167-2991(01)81974-1.

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Ghosh, Sangeeta, Paramita Hajra, Debasis Sariket, Debasish Ray, Swarnendu Baduri, and Chinmoy Bhattacharya. "Modifications of BiVO4 Semiconductors for Oxidation of Water and Detoxification of Organic Waste." In Innovative Nanocomposites for the Remediation and Decontamination of Wastewater. IGI Global, 2022. http://dx.doi.org/10.4018/978-1-6684-4553-2.ch001.

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The photoelectrochemical water splitting process has a lucid and efficacious impact, which emulates the natural photosynthesis process by converting solar energy into chemical energy. The construction of a PEC system can convert H2O to H2 or CO2 to C-based fuels. To achieve artificial photosynthesis, rate-determining kinetics of the OER is regarded as a highly efficient photo-anode. BiVO4 grabbed strong attention as a photoanode in the communal of PEC. Owing to a moderate bandgap and the Earth-abundant nature of the constituents, it is considered an inexpensive n-type semiconductor for PEC H2O

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Akindeji Jerome, Sabejeje, Adebare Nurudeen Adewumi, Yi Cheng Yi, Huaneng Su, and Lindiwe Khotseng. "Preparation and Characterization of Pd Nanoparticles Supported on Graphene-Based Anode Catalysts for Direct Methanol Fuel Cells." In Methanol Fuel in Transportation Sector and Fuel Cells [Working Title]. IntechOpen, 2024. http://dx.doi.org/10.5772/intechopen.1005441.

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Palladium (Pd) nanoparticles supported by graphene nanomaterials were prepared and tested in this work using methanol as the fuel. The synthesized nanoparticles were used as electrocatalysts for direct methanol fuel cell. The support materials were synthesized by modified Hummer’s method and subsequently doped with nitrogen using melamine. The electrocatalysts were synthesized using modified polyol method. The synthesis method of the electrocatalyst was further modified by adjusting the pH of the electrocatalyst from 12 to 13. The structural characterization of the support materials was carrie

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Conference papers on the topic "Kinetics; Oxidation; DMF (N"

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Qin, Wentao, Esteban Ortiz, Brandon Lent, et al. "High Contact Resistance from Preferential Oxidation of Silane Gas." In ISTFA 2024. ASM International, 2024. http://dx.doi.org/10.31399/asm.cp.istfa2024p0447.

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Abstract High resistance failures in P+ and N+ contact chains were traced to contacts partially filled with silicon dioxide (SiO2) instead of the intended tungsten. Investigation revealed that oxygen (O2) entered the deposition chamber through a faulty valve during silane gas (SiH4) flow for tungsten seed deposition. This contamination triggered a gas-phase reaction producing SiO2 particles that partially filled the contacts. Analysis of reaction kinetics explained the predominance of SiO2 formation over tungsten deposition: the bond dissociation energy for SiO2 formation is lower than that fo

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Bischoff, J., A. T. Motta, Y. Chen, and T. R. Allen. "Oxidation of 9Crods Exposed to Supercritical Water." In CORROSION 2009. NACE International, 2009. https://doi.org/10.5006/c2009-09248.

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Abstract The oxide layers formed on 9CrODS have been characterized using synchrotron radiation fluorescence and diffraction. This analysis showed a three-layer structure with an outer layer containing only Fe3O4, an inner layer containing a mixture of FeCr2O4 and Fe3O4, and a diffusion layer containing a mixture of metal grains and FeCr2O4 precipitates. A Cr2O3 ribbon formed at the diffusion layer-metal interface on the samples exposed to 600°C supercritical water for 4 and 6 weeks. Calculations of the oxidation behavior were undertaken to calculate the activation energy and the corrosion rate

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Andresen, Peter L. "Mechanisms & Modeling of Water Chemistry Effects in Inconels & Stainless, Low Alloy & Carbon Steels in High Temperature Water." In CORROSION 1989. NACE International, 1989. https://doi.org/10.5006/c1989-89566.

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Abstract The kinetics of environmental cracking of iron- and nickel-base alloys exposed to high temperature water is governed by water and material chemistry as well as by stressing parameters. A unifying, quantitative model based on evaluation of the crack tip ion activities is derived to account for the effects of water chemistry (water purity and corrosion potential), convective contributions (external fluid velocity and mechanical cycling), and material chemistry (metallurgical impurities). The subsequent effect on oxidation kinetics of crack tip solution chemistry and material chemistry (

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Dagaut, Philippe, and Sandro Gai¨l. "Kinetics of Gas Turbine Liquid Fuels Combustion: Jet-A1 and Bio-Kerosene." In ASME Turbo Expo 2007: Power for Land, Sea, and Air. ASMEDC, 2007. http://dx.doi.org/10.1115/gt2007-27145.

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The oxidation of kerosene and bio-kerosene (kerosene-rapeseed oil methyl esters 80/20 in mole) was studied experimentally in a jet-stirred reactor at 10 atm and constant residence time, over the high temperature range 740-1200 K, and for variable equivalence ratios in the range 0.5–1.5. Concentration profiles of reactants, stable intermediates, and final products were obtained by probe sampling followed by on-line and off-line GC analyses. The oxidation of these fuels in these conditions was modeled using a detailed kinetic reaction mechanism consisting of 2027 reversible reactions and 263 spe

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Dagaut, Philippe. "Kinetics of Kerosene Combustion Over Extended Conditions: Experimental and Modeling." In ASME Turbo Expo 2006: Power for Land, Sea, and Air. ASMEDC, 2006. http://dx.doi.org/10.1115/gt2006-90015.

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The oxidation of kerosene (Jet-A1) and that of surrogate mixtures have been studied experimentally in a jet-stirred reactor at 1 to 40 atm and constant residence time, over the high temperature range 800–1300 K, and for variable equivalence ratio 0.5&lt;φ&lt;2). Concentration profiles of the reactants, stable intermediates, and final products have been obtained by probe sampling followed by on-line and off-line GC analyses. The oxidation of kerosene in these conditions was modeled using a detailed kinetic reaction mechanism (209 species and 1673 reactions, most of them reversible). In

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Guler, Mehmet Oguz, Mirac Alaf, Deniz Gultekin, Hatem Akbulut, and Ahmet Alp. "Oxidation Kinetics of Nano Crystalline Tin Oxide Conductive Thin Films." In ASME 2008 2nd Multifunctional Nanocomposites and Nanomaterials International Conference. ASMEDC, 2008. http://dx.doi.org/10.1115/mn2008-47072.

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Tin oxide was the first transparent conductor to have achieved significant commercialization. SnO2 is an n-type semiconductor with an optical band gap of about 3.6 eV in poly crystalline form. One of the main reasons for the wide use is its rather desirable characteristic of having both, high optical transmittance and high electrical conductivity. Under optimum deposition conditions, tin oxide crystallizes in the tetragonal (rutile) structure. In this study, nano crystalline thin oxide conductive thin films has been manufactured by thermal evaporation techniques onto steel substrates using met

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Donato, Nicole, Christopher Aul, Eric Petersen, Christopher Zinner, Henry Curran, and Gilles Bourque. "Ignition and Oxidation of 50/50 Butane Isomer Blends." In ASME Turbo Expo 2009: Power for Land, Sea, and Air. ASMEDC, 2009. http://dx.doi.org/10.1115/gt2009-59673.

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One of the alkanes found within gaseous fuel blends of interest to gas turbine applications is butane. There are two structural isomers of butane, normal butane and iso-butane, and the combustion characteristics of either isomer are not well known. Of particular interest to this work are mixtures of n-butane and iso-butane. A shock-tube experiment was performed to produce important ignition delay time data for these binary butane isomer mixtures which are not currently well studied, with emphasis on 50–50 blends of the two isomers. These data represent the most extensive shock-tube results to

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Loparo, Zachary E., Joseph G. Lopez, Sneha Neupane, Subith S. Vasu, William P. Partridge, and Konstantin Vodopyanov. "Time-Resolved Measurements of Intermediate Concentrations in Fuel-Rich n-Heptane Oxidation Behind Reflected Shock Waves." In ASME Turbo Expo 2017: Turbomachinery Technical Conference and Exposition. American Society of Mechanical Engineers, 2017. http://dx.doi.org/10.1115/gt2017-63344.

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The chemical kinetics of the oxidation of n-heptane (C7H16) — an important reference compound for real fuels — are well studied at stoichiometric and lean conditions. However, there is only limited information on the chemical kinetics of fuel-rich combustion. In order to improve the accuracy of chemical kinetic models at these conditions, the oxidation of rich n-heptane mixtures has been investigated. Combustion of n-C7H16/O2/Ar mixtures at equivalence ratios, ϕ, of 2.0 behind reflected shock waves has been studied at temperatures ranging from 1075 to 1418K and at pressures ranging from 1.6 to

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Gromov, Mikhail, Kseniia Leonova, Nikolay Britun, et al. "N₂ Oxidation Pathways in a ns-Pulsed Discharge Above Water: O Atoms, No, and Oh Radicals Kinetics." In 2021 IEEE International Conference on Plasma Science (ICOPS). IEEE, 2021. http://dx.doi.org/10.1109/icops36761.2021.9588569.

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Slavinskaya, N. A., A. Zizin, and U. Riedel. "Towards Surrogate Reaction Model Development." In ASME 2011 Turbo Expo: Turbine Technical Conference and Exposition. ASMEDC, 2011. http://dx.doi.org/10.1115/gt2011-45198.

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The present paper describes the proposed strategy of fuel model design based on identification of chemical and physical criteria for the selection of initial formula of the reference fuel. The first 8 criteria established and studied in previous papers so far are combustion enthalpy, formation enthalpy, molecular weight, C/H-ratio, sooting tendency index, critical point, two-phase diagram, and distillation curve. With these criteria established, the following candidate formula of the kerosene surrogate blend is defined and optimized to adequately mimic the properties of the real fuel: 10% n-pr

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