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Determination of furan and furan derivatives in baby food

Food Chemistry, 2018
A Headspace-Solid Phase Microextraction-Gas Chromatography-Mass Spectrometry (HS-SPME-GC-MS) method was developed and validated for the simultaneous determination of furan, 2-methylfuran, 2-ethylfuran, 2-butylfuran, 2-pentylfuran, 2-acetylfuran, furfural and furfuryl alcohol in jarred baby food. The method was specific for the analytes.
Concetta Condurso   +2 more
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Furans in foods

C R C Critical Reviews in Food Science and Nutrition, 1979
Furan represent a class of compounds that have been reported in a wide variety of foods. Normally, they result from thermal decomposition reactions, and, as such, are important in foods. They also possess unique sensory properties and, thus, can significantly contribute to food flavor.
Joseph A. Maga, Ira Katz
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Fun with Furans

ChemInform, 2004
AbstractFor Abstract see ChemInform Abstract in Full Text.
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Furans

2014
International audience ; Polymer networks derived from furan monomers are discussed, with particular emphasis on recent contributions. Resins based on furfural and furfuryl alcohol represent the most important family within this context, but other materials are becoming relevant, such as polyurethane foams, various photo-curable macromolecules bearing ...
Gandini, A., Belgacem, M.N.
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Furans

ChemInform, 2003
AbstractFor Abstract see ChemInform Abstract in Full Text.
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The Conversion of Furans into Phosphinines

Chemistry – A European Journal, 2011
AbstractThe [4+2] cycloadducts between furan compounds and a methylenechlorophosphane pentacarbonyltungsten complex are converted into the corresponding 2‐hydroxy‐ or 2‐bromophosphinine complexes by treatment with BBr3 and triethylamine. The X‐ray crystal structure of the parent 2‐phosphaphenol complex shows that the hydroxy substituent is coplanar ...
Yanli, Mao, François, Mathey
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Electron collisions with furan

The Journal of Chemical Physics, 2007
The authors report integral, differential and momentum transfer cross sections for elastic scattering of low-energy electrons by C4H4O (furan) molecules. Their calculations employed the Schwinger multichannel method with pseudopotentials and were performed in the static-exchange and in the static-exchange plus polarization approximations.
M H F, Bettega, M A P, Lima
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Reactivity Trends in Furan and Alkyl Furan Combustion

Energy & Fuels, 2014
A systematic study of the ignition behavior of furan and the substituted furans 2-methyl furan (2-MF) and 2,5-dimethyl furan (DMF) is presented. Ignition delay times are measured over a temperature range from 977 to 1570 K and pressures up to 12 atm for lean, stoichiometric, and rich mixtures of fuel, oxygen, and argon.
Mazen A. Eldeeb, Benjamin Akih-Kumgeh
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The Electronic Spectrum of Furan

Journal of the American Chemical Society, 1998
The 30 lowest electronic states of furan have been investigated with theoretical calculations (up to approximately 8.3 eV), and the experimental spectrum scrutinized in the relevant energy region.
Christiansen, O., Jørgensen, Poul
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