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oil content and physicochemical characteristics of oils

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SGt 2 −0.<br />

0006X<br />

+ SGt1<br />

= (Wan Nik et al., 2007), where X is the variation <strong>of</strong> temperature in degrees.<br />

This linearity is more reliable around the interval <strong>of</strong> 10 degrees (Kabele, 1975). This will allow<br />

comparing plant <strong>oil</strong> SG with different products such as fuel.<br />

3.2.3.2. Melting point<br />

The complete melting point (Cmp) <strong>of</strong> the <strong>oil</strong>s was determined using a fusiometer (Baur, 1995). The<br />

mpt is defined as the temperature at which a column <strong>of</strong> <strong>oil</strong> in an open capillary tube moves up the<br />

tube when it is subjected to controlled heating in a water bath (APOC, 2004). To determine the Cmp,<br />

a melting point capillary tube was filled with <strong>oil</strong> from the open end <strong>of</strong> tube. The capillary was placed<br />

in the melting point apparatus through one <strong>of</strong> the side tubes so that the sealed end <strong>of</strong> the capillary<br />

was touching the front <strong>of</strong> the mercury reservoir <strong>of</strong> the thermometer <strong>and</strong> begins to heat the apparatus<br />

with a micro burner. Thereafter burner was placed under the back end <strong>of</strong> the <strong>oil</strong> bath <strong>of</strong> the<br />

apparatus. The melting range was recorded when <strong>oil</strong> start dropping until when all <strong>oil</strong> has empty the<br />

capillary tube. The Cmp is recorded when the <strong>oil</strong> empty the capillary tube.<br />

3.2.3.3. Saponification value<br />

Two grams <strong>of</strong> the <strong>oil</strong> sample were introduced in a flask containing 30ml <strong>of</strong> ethanolic KOH (0.5 M)<br />

<strong>and</strong> heated under a reversed condenser for 30 minutes to ensure that the sample was fully dissolved.<br />

The sample was then cooled. One ml <strong>of</strong> phenolphthalein was added <strong>and</strong> titrated with 0.5 M HCl<br />

until a pink endpoint was reached. The same procedure was repeated with a blank, i.e. a flask with<br />

30ml <strong>of</strong> ethanolic KOH (0.5 M) but without <strong>oil</strong>. The saponification value was computed using the<br />

C1<br />

− C2<br />

formula: SV X 28<br />

M<br />

= , where C1 = number <strong>of</strong> ml <strong>of</strong> the Hydrochloric acid (0.5 M) used in<br />

blank, C2 = number <strong>of</strong> ml <strong>of</strong> the Hydrochloric acid used in the assay, M = mass in g <strong>of</strong> <strong>oil</strong> used.<br />

42

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