200 research outputs found
Rate constant of the reaction of chlorine atoms with methanol over the temperature range 291â475 K
The rate constant of the reaction Cl + CH 3 OH ( k 1 ) has been measured in 500â950 Torr of N 2 over the temperature range 291â475 K. The rate constant determination was carried out using the relative rate technique with C 2 H 6 as the reference compound. Experiments were performed by irradiating mixtures of CH 3 OH, C 2 H 6 , Cl 2 , and N 2 with UV light from a fluorescent lamp whose intensity peaked near 360 nm. The resultant temperature-dependent rate expression is k 1 = 8.6 (±1.3) Ă 10 â11 exp[â167 (±60)/T] cm 3 molecule â1 s â1 . Error limits represent data scatter (2ÎŁ) in the current experiments and do not include error in the reference rate constant. © 2009 Wiley Periodicals, Inc. Int J Chem Kinet 42: 113â116, 2010Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/64549/1/20474_ftp.pd
Estimation of rate coefficients and branching ratios for gas-phase reactions of OH with aliphatic organic compounds for use in automated mechanism construction
Reaction with the hydroxyl (OH) radical is the dominant removal process for volatile organic compounds (VOCs) in the atmosphere. Rate coefficients for reactions of OH with VOCs are therefore essential parameters for chemical mechanisms used in chemistry transport models, and are required more generally for impact assessments involving the estimation of atmospheric lifetimes or oxidation rates for VOCs. Updated and extended structureâactivity relationship (SAR) methods are presented for the reactions of OH with aliphatic organic compounds, with the reactions of aromatic organic compounds considered in a companion paper. The methods are optimized using a preferred set of data including reactions of OH with 489 aliphatic hydrocarbons and oxygenated organic compounds. In each case, the rate coefficient is defined in terms of a summation of partial rate coefficients for H abstraction or OH addition at each relevant site in the given organic compound, so that the attack distribution is defined. The information can therefore guide the representation of the OH reactions in the next generation of explicit detailed chemical mechanisms. Rules governing the representation of the subsequent reactions of the product radicals under tropospheric conditions are also summarized, specifically their reactions with O2 and competing processes
Model Reactions Involving Ester Functional Groups during ThermoâOxidative Degradation of Biodiesel
Biodiesel is a renewable fuel used in diesel engines that is typically blended with diesel fuel. However, biodiesel is susceptible to oxidation, which has the potential to produce higher molecular weight materials that may adversely impact vehicle fuelâsystem performance. To investigate the chemical reactions potentially important in biodiesel oxidation, four different types of chemical reactions involving esters were studied: (1) ester formation (reactions of acids with alcohols), (2) alcoholysis (reactions of alcohols with esters), (3) acidolysis (reaction of acids with esters), and (4) ester exchange (reactions between two esters). Experiments with representative model compounds were used to evaluate these reactions at 90â°C with aeration; conditions previously used to simulate thermoâoxidative degradation during biodiesel aging. Reactions were monitored using gas chromatography, fourier transform infrared (FTIR) spectroscopy, and total acid number (TAN). Evidence is presented suggesting that alcoholysis and ester formation (Reactions 1 and 2), catalyzed by carboxylic acids, are important reactions of esters that could lead to larger molecules. Acidolysis (Reaction 3) proceeded at a comparatively slow rate and ester exchange reaction products (Reaction 4) were not detected under these aging conditions.Peer Reviewedhttps://deepblue.lib.umich.edu/bitstream/2027.42/151841/1/aocs12277_am.pdfhttps://deepblue.lib.umich.edu/bitstream/2027.42/151841/2/aocs12277.pd
Emissions of CO 2 , CO, NO x , HC, PM, HFC-134a, N 2 O and CH 4 from the global light duty vehicle fleet
Abstract Vehicle
Atmospheric chemistry of cyclohexanone: UV spectrum and kinetics of reaction with chlorine atoms
Absolute and relative rate techniques were used to study the reactivity of Cl atoms with cyclohexanone in 6 Torr of argon or 800â950 Torr of N 2 at 295 ± 2 K. The absolute rate experiments gave k (Cl + cyclohexanone) = (1.88 ± 0.38) Ă 10 â10 , whereas the relative rate experiments gave k (Cl + cyclohexanone) = (1.66 ± 0.26) Ă 10 â10 cm 3 molecule â1 s â1 . Cyclohexanone has a broad UV absorption band with a maximum cross section of (4.0 ± 0.3) Ă 10 â20 cm 2 molecule â1 near 285 nm. The results are discussed with respect to the literature data. © 2008 Wiley Periodicals, Inc. Int J Chem Kinet 40: 223â229, 2008Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/58072/1/20291_ftp.pd
Reaction of Perfluorooctanoic Acid with Criegee Intermediates and Implications for the Atmospheric Fate of Perfluorocarboxylic Acids
The reaction of perfluorooctanoic
acid with the smallest carbonyl
oxide Criegee intermediate, CH<sub>2</sub>OO, has been measured and
is very rapid, with a rate coefficient of (4.9 ± 0.8) Ă
10<sup>â10</sup> cm<sup>3</sup> s<sup>â1</sup>, similar
to that for reactions of Criegee intermediates with other organic
acids. Evidence is shown for the formation of hydroperoxymethyl perfluorooctanoate
as a product. With such a large rate coefficient, reaction with Criegee
intermediates can be a substantial contributor to atmospheric removal
of perfluorocarboxylic acids. However, the atmospheric fates of the
ester product largely regenerate the initial acid reactant. Wet deposition
regenerates the perfluorocarboxylic acid via condensed-phase hydrolysis.
Gas-phase reaction with OH is expected principally to result in formation
of the acid anhydride, which also hydrolyzes to regenerate the acid,
although a minor channel could lead to destruction of the perfluorinated
backbone
Review of electrofuel feasibilityâcost and environmental impact
Electrofuels, fuels produced from electricity, water, and carbon or nitrogen, are of interest as substitutes for fossil fuels in all energy and chemical sectors. This paper focuses on electrofuels for transportation, where some can be used in existing vehicle/vessel/aircraft fleets and fueling infrastructure. The aim of this study is to review publications on electrofuels and summarize costs and environmental performance. A special case, denoted as bio-electrofuels, involves hydrogen supplementing existing biomethane production (e.g. anaerobic digestion) to generate additional or different fuels. We use costs, identified in the literature, to calculate harmonized production costs for a range of electrofuels and bio-electrofuels. Results from the harmonized calculations show that bio-electrofuels generally have lower costs than electrofuels produced using captured carbon. Lowest costs are found for liquefied bio-electro-methane, bio-electro-methanol, and bio-electro-dimethyl ether. The highest cost is for electro-jet fuel. All analyzed fuels have the potential for long-term production costs in the range 90-160 ⏠MWh-1. Dominant factors impacting production costs are electrolyzer and electricity costs, the latter connected to capacity factors (CFs) and cost for hydrogen storage. Electrofuel production costs also depend on regional conditions for renewable electricity generation, which are analyzed in sensitivity analyses using corresponding CFs in four European regions. Results show a production cost range for electro-methanol of 76-118 ⏠MWh-1 depending on scenario and region assuming an electrolyzer CAPEX of 300-450 ⏠kWelec-1 and CFs of 45%-65%. Lowest production costs are found in regions with good conditions for renewable electricity, such as Ireland and western Spain. The choice of system boundary has a large impact on the environmental assessments. The literature is not consistent regarding the environmental impact from different CO2 sources. The literature, however, points to the fact that renewable energy sources are required to achieve low global warming impact over the electrofuel life cycle
Review of electrofuel feasibility - Prospects for road, ocean, and air transport
To meet climate targets the emissions of greenhouse gases from transport need to be reduced considerably. Electrofuels (e-fuels) produced from low-CO2 electricity, water, and carbon (or nitrogen) are potential low-climate-impact transportation fuels. The purpose of this review is to provide a technoeconomic assessment of the feasibility and potential of e-fuels for road, ocean, and air transport. The assessment is based on a review of publications discussing e-fuels for one or more transport modes. For each transport mode, (a) e-fuel options are mapped, (b) cost per transport unit (e.g. vehicle km) and carbon abatement costs are estimated and compared to conventional options, (c) prospects and challenges are highlighted, and (d) policy context is described. Carbon abatement costs for e-fuels (considering vehicle cost, fuel production and distribution cost) are estimated to be in the range 110-1250 ⏠tonne-1 CO2 with e-gasoline and e-diesel at the high end of the range. The investigated combined biofuel and e-fuels production pathways (based on forest residues and waste) are more cost-competitive than the stand-alone e-fuel production pathways, but the global availability of sustainable biomass is limited making these pathways more constrained. While the potential for e-fuels to decarbonize the transport sector has been discussed extensively in the literature, many uncertainties in terms of production costs, vehicle costs and environmental performance remain. It is too early to rule out or strongly promote particular e-fuels for different transport modes. For e-fuels to play a significant role in transportation, their attractiveness relative to other transport options needs to be improved. Incentives will be needed for e-fuels to be cost-effective and increased clarity on how e-fuels are linked to existing policies is needed
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Evaluated kinetic and photochemical data for atmospheric chemistry: Volume VII-Criegee intermediates
This article, the seventh in the series, presents kinetic and photochemical data sheets evaluated by the IUPAC Task Group on Atmospheric Chemical Kinetic Data Evaluation. It covers an extension of the gas-phase and photochemical reactions related to Criegee intermediates previously published in Atmospheric Chemistry and Physics (ACP) in 2006 and implemented on the IUPAC website up to 2020. The article consists of an introduction, description of laboratory measurements, a discussion of rate coefficients for reactions of O3 with alkenes producing Criegee intermediates, rate coefficients of unimolecular and bimolecular reactions and photochemical data for reactions of Criegee intermediates, and an overview of the atmospheric chemistry of Criegee intermediates. Summary tables of the recommended kinetic and mechanistic parameters for the evaluated reactions are provided. Data sheets summarizing information upon which the recommendations are based are given in two files, provided as a Supplement to this article. © Author(s) 2020
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Henryâs law constants (IUPAC Recommendations 2021)
Article presenting a consistent set of recommendations to express the proportionality coefficient, âHenryâs law constantâ of Henry's law
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