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The genus Cinnamomum

The genus Cinnamomum

The genus Cinnamomum

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140 K.R. Dayananda, U.M. Senanayake and R.O.B. Wijesekera<br />

(Tiwari, 1989). CO 2 is the most commonly employed SCF. CO 2 is available freely, it<br />

is cheap, non-flammable, non-toxic and non-corrosive. It behaves either as a polar or<br />

non-polar solvent depending on pressure and temperature employed. CO 2 is liquid<br />

below its critical point (31.2 °C, 7.38 milli pascal pressure) and above that it exists as<br />

a super critical fluid. <strong>The</strong> technical advantages of using SCFE for spices were studied<br />

by Udayasankar (1989).<br />

Coarsely ground cinnamon bark is extracted with supercritical CO 2 using pressures<br />

of 300, 400, 500 and 600 bar. <strong>The</strong> yield is around 1.4% as compared to steam distilled<br />

(0.5–0.8%). No significant differences were reported sensorily between the SCF extract<br />

and steam distilled oil and extracts (Pruthi, 2001). L CO 2 extract of powdered bark is<br />

a mobile oil without the dark coloured waxes and resins normally encountered with<br />

the bark oleoresin prepared with chemical organic solvent. <strong>The</strong> CO 2 selective extract is<br />

more soluble in foods, while the resinous compounds have a slight fixing effect on the<br />

flavour components of cinnamon and cassia bark extracts. However, the SCFE process<br />

is not practiced for commercial cinnamon or cassia oleoresin production because the<br />

process is very costly and the product does not differ much in quality from the solvent<br />

extracted product.<br />

Cinnamon oleoresin<br />

Oleoresins are solvent extracts of spices that contain the volatile oil, non-volatile resinous<br />

material and the active ingredient that characterises the spice as hot or pungent when<br />

such an ingredient is present. <strong>The</strong> solvents commonly used for the preparation of the<br />

oleoresins are acetone, ether, ethanol, propanol or methylene chloride. Ethanol was at one<br />

time the preferred solvent but is no longer used due to its high cost. Acetone is now the<br />

most commonly used solvent for oleoresin production. In solvent extraction the selected<br />

solvent is allowed to percolate down through coarsely ground spice which is loaded in a<br />

percolator. <strong>The</strong> bottom drain of the percolator is kept open for the escape of air. When all<br />

the material is soaked the bottom drain is closed and sufficient contact time is given to<br />

reach the solutes into the solvent. After the contact time, the extract, called “micella”, is<br />

drained and collected.<br />

For oleoresin production either the Soxhlet extraction method or the batch counter<br />

current extraction method (CCE) is industrially practiced. In the Soxhlet method the<br />

solvent is allowed to percolate through the bed of material several times, which involves<br />

continuous heating of the extract. In the CCE method, which is very widely used, the<br />

powdered spice is packed in to a series of extractors and extracted with a suitable<br />

selected solvent. <strong>The</strong> solvent moves from extractor to extractor and the dilute extract is<br />

allowed to percolate through the spice. <strong>The</strong> concentrated extract obtained first from<br />

each extractor is withdrawn for solvent removal in the production of oleoresin.<br />

<strong>The</strong> micelle obtained from the extractor is distilled to get the finished product. Most<br />

of the solvent (90–95%) present in the micella is recovered by normal atmospheric<br />

pressure distillation, while the remaining solvent is taken off by distillation under<br />

reduced pressure. <strong>The</strong> trace amounts of solvent are finally removed by either the<br />

azeotropic or extractive distillation method using an innocuous solvent like ethyl<br />

alcohol. Alternatively, bubbling nitrogen into the thick viscous material is carried out<br />

to drive away the residual solvent. <strong>The</strong> maximum permitted residual limits for some of<br />

the solvents are 30 ppm for acetone and chlorinated solvents, 50 ppm for methyl<br />

alcohol and isopropyl alcohol and 25 ppm for hexane (CFR, 1995). After distillation

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