| Literature DB >> 29296263 |
Sara Moradi1, Alireza Fazlali1, Hamid Hamedi2.
Abstract
BACKGROUND: Hydro-distillation (HD) method is a traditional technique which is used in most industrial companies. Microwave-assisted Hydro-distillation (MAHD) is an advanced HD technique utilizing a microwave oven in the extraction process.Entities:
Keywords: Essential Oil; Hydro distillation; Microwave distillation; Rosemary
Year: 2018 PMID: 29296263 PMCID: PMC5742650
Source DB: PubMed Journal: Avicenna J Med Biotechnol ISSN: 2008-2835
Figure 1.MAHD apparatus used in this study.
Concentrations of the essential oil of Rosemary compounds obtained by different methods
| Tricyclene | 9.84 | 926 | 922 | 0.07 | 0.05 | - | - | |
| a-Thujene | 13.39 | 931 | 926 | 0.31 | 0.25 | 0.21 | 0.28 | |
| a-Pinene | 13.61 | 939 | 930 | 24.24 | 20.02 | 17.95 | 22.74 | |
| Camphene | 13.96 | 953 | 950 | 7.51 | 6.4 | 5.35 | 6.95 | |
| β-pinene | 14.02 | 980 | 976 | 4.27 | 4.79 | 4.32 | 5.59 | |
| 1-octen-3-ol | 14.28 | 978 | 975 | 0.34 | 0.49 | 0.41 | 0.5 | |
| β-myrcene | 14.36 | 991 | 985 | 2.48 | 2.3 | 2.14 | 2.37 | |
| α-phellandrene | 14.52 | 1005 | 1000 | 0.33 | 0.3 | 0.26 | 0.3 | |
| 3-carene[ | 14.97 | 1011 | 1008 | 0.05 | 0.15 | 0.13 | - | |
| α-terpinene | 15.20 | 1018 | 1015 | 1.64 | 1.59 | 1.52 | 1.38 | |
| P-cymene | 15.44 | 1026 | 1022 | 3.74 | 3.5 | 3.46 | 3.52 | |
| 1,8-cineole[ | 15.52 | 1032 | 1030 | 8.79 | 9.35 | 8.84 | 9.34 | |
| Cis-Ocimene | 15.92 | 1040 | 1036 | 0.09 | 0.08 | - | 0.09 | |
| β-Ocimene | 16.13 | 1050 | 1045 | 0.05 | 0.06 | - | - | |
| γ-terpinene | 16.45 | 1062 | 1060 | 2.36 | 3.49 | 3.33 | 3.28 | |
| cis-Sabinene hydrate[ | 16.72 | 1067 | 1065 | 0.69 | 0.74 | 0.66 | 0.74 | |
| Terpinolene | 17.15 | 1088 | 1085 | 0.32 | 0.38 | 0.3 | 0.22 | |
| Linalool | 17.73 | 1098 | 1090 | 10.98 | 11.99 | 12.19 | 12.13 | |
| Fenchol | 17.80 | 1115 | 1110 | 0.06 | 0.07 | - | - | |
| Campholaldehyde[ | 17.96 | 1124 | 1120 | 2.13 | 2.35 | 2.39 | 2.23 | |
| Camphor | 18.20 | 1143 | 1140 | 7.56 | 8.75 | 8.86 | 8.06 | |
| Isopulegol | 18.28 | 1145 | 1147 | 1.49 | 1.71 | 1.8 | 1.62 | |
| Pinocamphone/isopinocamphone | 18.46 | 1160 | 1162 | 1.83 | 2.15 | 2.24 | 1.91 | |
| Pinocarvone/trans-pinocarvone | 18.60 | 1162 | 1164 | 1.25 | 1.48 | 1.56 | 1.32 | |
| Borneol | 18.81 | 1165 | 1167 | 11.28 | 11.53 | 15.38 | 10.39 | |
| 4-terpineol[ | 19.25 | 1177 | 1175 | 0.19 | 0.21 | 0.23 | 0.2 | |
| p-cymene-8-ol | 19.41 | 1183 | 1180 | 0.77 | 0.95 | 1.01 | 0.82 | |
| α-terpineol | 19.55 | 1189 | 1185 | 1.17 | 1.39 | 1.43 | 1.25 | |
| Myrtenol | 19.72 | 1194 | 1195 | 0.04 | 0.05 | 0.13 | - | |
| Verbenone | 20.16 | 1204 | 1200 | 1.49 | 1.66 | 1.72 | 1.33 | |
| Citronellol | 20.60 | 1228 | 1225 | 0.04 | 0.05 | - | - | |
| Bornyl acetate | 20.99 | 1285 | 1280 | 0.33 | 0.29 | 0.42 | 0.27 | |
| Carvacrol | 21.40 | 1298 | 1295 | 0.27 | 0.05 | - | - | |
| Methyl eugenol | 21.54 | 1401 | 1400 | 0.13 | 0.1 | - | 0.08 | |
| β-caryophyllene | 22.93 | 1418 | 1415 | 0.3 | 0.5 | 0.59 | 0.49 | |
| α-humulene | 23.44 | 1453 | 1450 | 0.06 | 0.08 | - | 0.11 | |
| Methyl jasmonate | 25.57 | 1647 | 1650 | 0.1 | 0.13 | 0.19 | 0.14 | |
| Others | 26.52 | 0.35 | 0.35 | 0.51 | 0.29 | |||
NI : Not identified,
Literature,
Experimental
Figure 2.Extraction yield as a function of time for the hydro-distillation. (HD) and microwave-assisted hydro-distillation (MAHD) of essential oils from thyme aerial parts.
Figure 3.Chromatography of Rosemary essential oil by HD.
Figure 4.Chromatography of Rosemary essential oil by MAHD.
Figure 5.Comparison between chemical compositions of rosemary extracts isolated through the different processes. HC=hydrocarbons, OX=oxygenated.
Percent of chemical components of rosemary extracts by different methods
| 47.00 | 42.84 | 38.67 | 46.39 | |
| 50.88 | 55.44 | 59.46 | 52.33 | |
| 0.36 | 0.58 | 0.59 | 0.6 |