Fractioning of orange (Citrus sinensis L.) essential oil using vacuum fractional distillation

References

• Escobar, C.A.L.; Castro, M.D.L. (2014). Towards a comprehensive exploitation of Citrus. Trends in Food Science & Technology, 39: 63–75 .
   Web of Science ®Google Scholar
• Rowe, D.J. (2005). Chemistry and Technology of Flavors and Fragrances. Blackwell Publishing: Poole, Uk. p. 336.
   Google Scholar
• López-Muñoz, G.A.; Balderas-López, J.A. (2014). Photothermal characterization of citrus essential oils and their derivatives. Thermochimica Acta, 579: 40–44.
   Web of Science ®Google Scholar
• Simões, C.M.O. et al. (2001). Farmacognosia: da planta ao medicamento. 3rd ed. Porto Alegre: Editora da Ufsc. p. 833.
   Google Scholar
• Martins, P.F.; Medeiros, H.H.R.; Sbaite, P.; Wolf Maciel, M.R. (2013). Enrichment of oxyterpenes from orange oil by short path evaporation. Separation and Purification Technology, 116: 385–390.
   Web of Science ®Google Scholar
• Hosni, K.; Zahed, N.; Chrif, R.; Abid, I.; Medfei, W.; Kallel, M.; Brahim, N.B.; Sebei, H.; (2010). Composition of peel essential oils from four selected Tunisian Citrus species: evidence for the genotypic influence. Food Chemistry, 123: 1098–1104.
   Web of Science ®Google Scholar
• Buhl, D.; Roberge, D.M.; Hölderich, W.F. (1999). Production of p-cymene from a-limonene over silica supported Pd catalysts. Applied Catalysis A: General, 188: 287–299.
   Web of Science ®Google Scholar
• Gutiérrez, C.; Rodríguez, J.F.; Gracia, I.; De Lucas, A.; García, M.T. (2014). Preparation and characterization of polystyrene foams from limonene solutions. The Journal of Supercritical Fluids, 88: 92–104.
   Web of Science ®Google Scholar
• Casabianca, H.; Graff, J.B.; Faugier, V.; Fleig, F.; Grenier, C. (1998). Enantiomeric distribution studies of linalool and linalyl acetate: apowerful tool for authenticity control of essential oils. Journal of Separation Science, 21(2): 107–112.
   Google Scholar
• Environmental Protection Agency ( EPA). (2008). Biopesticides registration action document: Linalool. US Government, 27 p. Avaliable in: <http://www3.epa.gov/pesticides/chem_search/reg_actions/registration/decision_PC-128838_10-Jun-08.pdf>.
   Google Scholar
• Nakamura, A.; Fujiwara, S.; Matsumoto, I.; Abe, K. (2009). Stress repression in restrained rats by (R)-(-)-linalool inhalation and gene expression profiling of their whole blood cells. Journal of Agricultural and Food Chemistry, 57: 5480–5485.
   PubMed Web of Science ®Google Scholar
• Behr, A.; Johnen, L. (2009). Myrcene as a natural base chemical in sustainable chemistry: a critical review. ChemSusChem, 2(12): 1072–1095.
   PubMed Web of Science ®Google Scholar
• Panten, J.; Surburg, H. (2015). Flavors and fragrances, 1. general aspects. Ullman’s Encyclopedia of Industrial Chemistry. 1–9.
   Google Scholar
• Moncada, J.; Tamayo, J.A.; Cardona, C.A. (2016). Techno-economic and environmental assessment of essential oil extraction from oregano (Origanum vulgare) and rosemary (Rosmarinus officinalis) in Colombia. Journal of Cleaner Production, 112: 172–181.
   Web of Science ®Google Scholar
• Silva, R.P.F.F.; Rocha-Santos, T.A.P.; Duarte, A. (2016). Supercritical fluid extraction of bioactive compounds. Trends in Analytical Chemistry, 76: 40–51.
   Web of Science ®Google Scholar
• Vega, G.R.; Cervantes, M.A.S.; Alvarado, M.A.G. (2016). Fractionation of vanilla oleoresin by supercritical CO2 technology. The Journal of Supercritical Fluids, 108: 79–88.
   Web of Science ®Google Scholar
• Foust, A.S.; Wenzel, L.A.; Clump, C.W.; Maus, L.; Andersen, L.B. (1982). Principles of Unit Operations. 2nd ed. Rio de Janeiro: Guanabara Dois.
   Google Scholar
• Silvestre, W.P.; Agostini, F.; Muniz, L.A.R.; Pauletti, G.F. (2016). Fractioning of green mandarin (Citrus deliciosa Tenore) essential oil by vacuum fractional distillation. Journal of Food Engineering, 178: 90–94.
   Web of Science ®Google Scholar
• Stüker, C.Z.; Costa, I.M.; Placeres, A.; Gallucci, S.; Kato, V. (2011). Uso de destilação fracionada (DF) para obtenção de produtos diferenciados em perfumaria a partir de óleos essenciais de cítricos. Annals In: Reunião da Sociedade Brasileira de Química, 34, Florianópolis, SC.
   Google Scholar
• Farah, A.; Afifi, A.; Fechtal, M.; Chhen, A.; Satrani, B.; Talbi, M.; Chaouch, A. (2006). Fractional distillation effect on the chemical composition of Moroccan myrtle (Myrtus communis L.) essential oils. Flavour and Fragrance Journal, 21: 351–354.
   Web of Science ®Google Scholar
• Koshima, C.C. (2011). Desterpenação de Óleos Essenciais de Bergamota e Limão: Determinação de Dados de Equilíbrio Líquido - líquido e Modelagem Termodinâmica de Sistemas Modelo, a 25°C. Dissertation (Master degree) – Course of Engineering Sciences of Food Engineering, University of São Paulo, Pirassununga, Brazil. p. 100.
   Google Scholar
• Oliveira, S.M.M.; Jose, V.L.A. (2007). Dossiê Técnico: Processos de extração de óleos essenciais. Paraná: Tecpar.
   Google Scholar
• Gomes, M.S. (2011). Caracterização Química e Atividade Antifúngica dos Óleos Essenciais de Cinco Espécies do Gênero CITRUS. 2011. Dissertation (Master degree) – postgraduate course of Agrochemistry, Federal University of Lavras, Lavras – Brazil. p. 98.
   Google Scholar
• Wei, Q.; Keck, C.M.; Müller, R.H. (2016). Oral hesperidin—Amorphization and improved dissolution properties by controlled loading onto porous silica. International Journal of Pharmaceutics. doi:10.1016/j.ijpharm.2016.11.005.
   Web of Science ®Google Scholar
• Serafini, L.A. ( org.) (2003). Estudos de processos de extração de óleos essenciais e bioflavanóides de frutas cítricas. Caxias do Sul: Educs. p. 112.
   Google Scholar
• Singh; P.; Shukla, R.; Prakash, B.; Kumar, A.; Singh, S; Mishra, P.K.; Dubey, N.K. (2010). Chemical profile, antifungal, antiaflatoxigenic and antioxidant activity of Citrus maxima Burm. and Citrus sinensis (L.) Osbeck essential oils and their cyclic monoterpene, DL-limonene. Food and Chemical Toxicology, 48: 1734–1740.
   PubMed Web of Science ®Google Scholar
• Rowan, D.D.; Allen, J.M.; Fielder, S.; Spicer, J.A.; Brimble, M.A. (1995). Identification of Conjugated Triene Oxidation Products of .alpha.-Farnesene in Apple Skin. Journal of Agricultural and Food Chemistry, 43: 2040–2045.
   Web of Science ®Google Scholar
• Spicer, J.A., Brimble, M.A., Rowan, D.D. (1993). Oxidation of α-Farnesene. Australian Journal of Chemistry, 46: 1929–1939.
   Web of Science ®Google Scholar
• Larsen, B.R.; Lahaniati, M.; Calogirou, A.; Kotzias, D. (1998). Atmospheric oxidation products of terpenes: a new nomenclature. Chemosphere, 37: 1207–1220.
   Web of Science ®Google Scholar
• Librando, V.; Tringali, G. (2005). Atmospheric fate of OH initiated oxidation of terpenes. Reaction mechanism of α-pinene degradation and secondary organic aerosol formation. Journal of Environmental Management, 75: 275–282.
   PubMed Web of Science ®Google Scholar
• Calogirou, A.; Larsen, B.R.; Kotzias, D. (1999). Gas-phase terpene oxidation products: a review. Atmospheric Environment, 33: 1423–1439.
   Web of Science ®Google Scholar