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Shock-tube study of the ignition and product formation of fuel-rich CH4/air and CH4/additive/air mixtures at high pressure

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TLDR
In this paper, the ignition delay times of fuel-rich methane/(additive)/air mixtures were measured in a shock tube at about 30 bar and temperatures between 600 and 1650 K.
Abstract
Higher-value chemicals can be produced from methane with small exergy losses by partial oxidation if the chemical conversion proceeds in an internal combustion engine (ICE) as a polygeneration process (Gossler and Deutschmann, 2015). Kinetics models are not sufficiently validated for the very fuel-rich and high-pressure conditions relevant for this process. Therefore, ignition delay times of fuel-rich methane/(additive)/air mixtures were measured in a shock tube at about 30 bar and temperatures between 600 and 1650 K. n-heptane and diethylether were used as additives to increase the reactivity of the fuel so that the polygeneration process can be realized in an ICE at HCCI conditions at lower compression temperatures. At ϕ = 2, measured ignition delay times agree well with simulations using different mechanisms from literature. Synthesis gas (CO, H2) is the main product at these conditions (Sen et al., 2016). For the production of higher hydrocarbons, the equivalence ratio must be increased. Very fuel-rich mixtures (ϕ = 10) were used because the temperature increase during the reaction of these mixtures is quite low (

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Citations
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Power and syngas production from partial oxidation of fuel-rich methane/DME mixtures in an HCCI engine

TL;DR: In this article, a single-cylinder engine operated in homogeneous charge compression-ignition (HCCI) mode on a mixture of methane and air with dimethyl ether (DME) as a reactivityenhancing additive was used to generate synthesis gas.
Journal ArticleDOI

An experimental and modeling study on the reactivity of extremely fuel-rich methane/dimethyl ether mixtures

TL;DR: In this paper, an extended chemical kinetics mechanism was developed that also covers extremely fuel-rich conditions of methane/dimethyl ether mixtures, which is shown to predict well the ignition delay time and species concentration evolution measurements presented in this paper.
Journal ArticleDOI

Impact of shock-tube facility-dependent effects on incident- and reflected-shock conditions over a wide range of pressures and Mach numbers

TL;DR: In this article, the authors investigated the influence of geometry and operating procedures on the performance of four geometrically different shock tubes located in two laboratories, Texas A&M University and the University of Duisburg-Essen.
Journal ArticleDOI

Shock-tube study of methane pyrolysis in the context of energy-storage processes

TL;DR: In this article, the thermal decomposition of methane (10% in inert gases) was investigated behind reflected shock waves, and the results were compared to simulations based on three different literature mechanisms (Cai and Pitsch, 2015; Porras et al., 2017; Wang et al, 2007) as well as with the new rate constant of methane dissociation.
References
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Journal ArticleDOI

A Comprehensive Modeling Study of iso-Octane Oxidation

TL;DR: In this paper, a detailed chemical kinetic mechanism has been developed and used to study the oxidation of iso-octane in a jet-stirred reactor, flow reactors, shock tubes and in a motored engine.
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Kinetic modeling of gasoline surrogate components and mixtures under engine conditions

TL;DR: In this article, an improved version of the kinetic model was used to analyze the combustion behavior of several components relevant to gasoline surrogate formulation, focusing attention on the mixing effects of the fuel components.
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An ignition delay and kinetic modeling study of methane, dimethyl ether, and their mixtures at high pressures

TL;DR: In this article, both experimental and chemical kinetic model-predicted ignition delay time data are provided covering a range of conditions relevant to gas turbine environments (T = 600-1600 K, p = 7-41 K, ϕ ǫ = 0.3, 0.5, 1.0, and 2.0 in ‘air’ mixtures).
Journal ArticleDOI

A consistent chemical mechanism for oxidation of substituted aromatic species

TL;DR: In this paper, a consistent chemical mechanism to predict the high temperature combustion characteristics of toluene, styrene, ethylbenzene, 1,3-dimethylbenzenes (m-xylene), and 1-methylnaphthalene is presented.
Journal ArticleDOI

Optimized chemical mechanism for combustion of gasoline surrogate fuels

TL;DR: In this article, a reduced combustion mechanism of primary reference fuel (PRF) mixtures (n-heptane and iso-octane) is integrated into the published kinetic model, allowing for the formulation of multi-component surrogate fuels (e.g. PRF/toluene) and for the prediction of Polycyclic Aromatic Hydrocarbon (PAH) formation in gasoline engines.
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