Commercial turpentine oil enriched with α-terpineol using an acid heterogeneous catalyst
The hydration of α-pinene, limonene, β-pinene, and commercial turpentine oil in the presence of strong acidic cation exchange resin Amberlyst-15 was studied. The acid catalytic hydration was performed in a batch reactor, and the effect of solvent at various temperatures and reaction times was evalua...
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Published in: | Revista Facultad de Ingeniería |
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Universidad de Antioquia
01-07-2024
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Abstract | The hydration of α-pinene, limonene, β-pinene, and commercial turpentine oil in the presence of strong acidic cation exchange resin Amberlyst-15 was studied. The acid catalytic hydration was performed in a batch reactor, and the effect of solvent at various temperatures and reaction times was evaluated. The main hydration product obtained from α-pinene was α-terpineol with a yield of 36 % (4 h, 70 °C, 2-propanol as solvent); however, the selected catalytic system was even more active to obtain α-terpineol when β-pinene was used as a substrate, obtaining α-terpineol yield of 38 % in 2 h of reaction. For the hydration of turpentine (70 °C, turpentine:water:2-propanol mass ratio of 1:0.5:2, 15 % w/w catalyst) the composition of reaction mixture after 4 h was 35 % w/w of α-terpineol, 8 % w/w of α-pinene, and 0.5 % w/w of β –pinene, which correspond to a final content of α-terpineol similar to the concentration obtained when α-pinene was used as a substrate (36 % w/w). |
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AbstractList | The hydration of α-pinene, limonene, β-pinene, and commercial turpentine oil in the presence of strong acidic cation exchange resin Amberlyst-15 was studied. The acid catalytic hydration was performed in a batch reactor, and the effect of solvent at various temperatures and reaction times was evaluated. The main hydration product obtained from α-pinene was α-terpineol with a yield of 36 % (4 h, 70 °C, 2-propanol as solvent); however, the selected catalytic system was even more active to obtain α-terpineol when β-pinene was used as a substrate, obtaining α-terpineol yield of 38 % in 2 h of reaction. For the hydration of turpentine (70 °C, turpentine:water:2-propanol mass ratio of 1:0.5:2, 15 % w/w catalyst) the composition of reaction mixture after 4 h was 35 % w/w of α-terpineol, 8 % w/w of α-pinene, and 0.5 % w/w of β –pinene, which correspond to a final content of α-terpineol similar to the concentration obtained when α-pinene was used as a substrate (36 % w/w). |
Author | Aguas-Caballero, Iván de Jesús Villa-Holguín, Aída Luz Alarcón-Durango, Edwin Alexis |
Author_xml | – sequence: 1 givenname: Iván de Jesús surname: Aguas-Caballero fullname: Aguas-Caballero, Iván de Jesús – sequence: 2 givenname: Aída Luz orcidid: 0000-0002-3770-3223 surname: Villa-Holguín fullname: Villa-Holguín, Aída Luz – sequence: 3 givenname: Edwin Alexis orcidid: 0000-0001-5887-4016 surname: Alarcón-Durango fullname: Alarcón-Durango, Edwin Alexis |
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Cites_doi | 10.3390/molecules28073202 10.1002/9783527632220 10.1016/j.molcata.2008.09.017 10.1007/s10562-017-2267-2 10.1016/j.scp.2019.100207 10.14266/ajoct19-3 10.1016/j.supflu.2009.11.001 10.1021/jf010341b 10.2478/s11532-013-0217-4 10.1016/B978-0-12-386454-3.01034-4 10.1016/S1381-1169(01)00217-5 10.1016/j.cattod.2005.07.061 10.1016/j.molcata.2010.02.028 10.1016/j.cej.2011.01.037 10.1016/j.heliyon.2020.e04984 10.1002/kin.20416 10.1023/B:TOCA.0000013551.99872.8d 10.1039/J29710000668 10.1016/j.micromeso.2006.10.022 10.22146/ijc.21386 10.1016/1381-1169(95)00244-8 10.1021/acs.iecr.9b04848 10.22146/ijc.21327 10.1021/ja01201a026 10.1016/S0920-5861(99)00273-4 10.1021/ie50325a019 10.1016/j.catcom.2006.02.018 10.1016/j.cej.2006.09.004 10.1016/S0920-5861(01)00289-9 10.1021/ie060470n |
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Title | Commercial turpentine oil enriched with α-terpineol using an acid heterogeneous catalyst |
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