2013
DOI: 10.1016/j.fuel.2012.08.040
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A potential refinery process of light–light naphtha olefins conversion to valuable oxygenated products in aqueous media – Part 1: Biphasic hydroformylation

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Cited by 14 publications
(15 citation statements)
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“…RhCl 3 ·3H 2 O and TPPTS were purchased from Alfa Aesar and used as catalyst precursor and ligand for hydroformylation reactions, respectively (Kokkinos et al 2013). For the gaseous phase of the hydroformylation reactions, CO/H 2 (1/1) was used without further purification (Kokkinos et al 2013). For hydrogenation reactions, RuCl 3 ·xH 2 O (Aldrich) was used as catalyst precursor (Kokkinos et al 2013, Kokkinos et al 2015.…”
Section: Materials and Instrumentationmentioning
confidence: 99%
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“…RhCl 3 ·3H 2 O and TPPTS were purchased from Alfa Aesar and used as catalyst precursor and ligand for hydroformylation reactions, respectively (Kokkinos et al 2013). For the gaseous phase of the hydroformylation reactions, CO/H 2 (1/1) was used without further purification (Kokkinos et al 2013). For hydrogenation reactions, RuCl 3 ·xH 2 O (Aldrich) was used as catalyst precursor (Kokkinos et al 2013, Kokkinos et al 2015.…”
Section: Materials and Instrumentationmentioning
confidence: 99%
“…For the gaseous phase of the hydroformylation reactions, CO/H 2 (1/1) was used without further purification (Kokkinos et al 2013). For hydrogenation reactions, RuCl 3 ·xH 2 O (Aldrich) was used as catalyst precursor (Kokkinos et al 2013, Kokkinos et al 2015. For the gaseous phase of the hydrogenation reactions, hydrogen 5.0 N was used without further purification.…”
Section: Materials and Instrumentationmentioning
confidence: 99%
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