2017
DOI: 10.1016/j.apsusc.2017.05.136
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Oxidation of limonene using activated carbon modified in dielectric barrier discharge plasma

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Cited by 31 publications
(13 citation statements)
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“…Further, it is more intense than the G band, indicating there to be a large amount of highly disordered graphite (Bielza et al, 1999). The G band, in contrast, corresponds to graphitic carbon, which is more ordered, symmetrical, and crystalline (Cheng et al, 2016;Glonek et al, 2017). Figure 2 shows the FTIR spectrum for each of the activated carbons.…”
Section: Characterization Of the Active Carbons Producedmentioning
confidence: 99%
“…Further, it is more intense than the G band, indicating there to be a large amount of highly disordered graphite (Bielza et al, 1999). The G band, in contrast, corresponds to graphitic carbon, which is more ordered, symmetrical, and crystalline (Cheng et al, 2016;Glonek et al, 2017). Figure 2 shows the FTIR spectrum for each of the activated carbons.…”
Section: Characterization Of the Active Carbons Producedmentioning
confidence: 99%
“…The catalyst landscape is a hostile environment and is subjected to bombardment by ionised and energetic species including electrons and this will affect how the catalyst and its adsorbed species survive. It is well established that catalysts can be pre-treated by exposure to plasma for subsequent use in conventional thermal processing [44][45][46]. For example, using a low pressure glow discharge or radio frequency plasma with Ar, He, N 2 or air as a source of energetic electrons, it is possible to reduce a metal catalyst [47,48].…”
Section: The Catalytic Landscape As Seen By a Plasma Dischargementioning
confidence: 99%
“…According to literature reported data, the orange essential oil spectrum obtained in SE displays, for limonene (LIM), a peak at 274 [ 34 , 35 ] followed by a smaller one at 252 nm (the first row from Table 1 ). The splitting of absorption maximum can be caused especially by the appearance of hydrophobic interactions and/or due to the limonene susceptibility to oxidation, during storage, at one or both double bonds leading to the formation of some compounds such as oxides, peroxides, or alcohols [ 36 , 37 ].…”
Section: Resultsmentioning
confidence: 99%