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Table 1. Characterization ofAfze//a africana seed oil may be grouped as a semi-drying oil (Norris, 1965).
This value also places the oil as highly unsaturated
Parameter Value
and as an oleic-linoleic-acid oil (Norris, 1965). The
Oil content (% of dry seeds) 25.80 __+2.00 low acid value and free fatty acid value of the oil
Saponification value (rag/g) 17.74___1.25 also showed the oil to be an oil with a long shelf-life,
Iodine value (g/100 g) 104.46__+2-22 which should not need much purification.
Acid value (mg/g) 1-96+0.11 The property of unsaturation suggested the use of
Free fatty acid (mg/g) 0.98 + 0.06
Specific gravity at room temp. (28C) 0-92 the Afzelia africana seed oil for the formulation of
Mean molecular mass 3162-35 alkyd resin. The oil yielded a good resin on heating
above 250C. The resin was used as part of the
formulation of paint. The oil itself could also be
used for other purposes, such as a constituent of
cobalt naphthenate (1.24%) were all mixed in a con- shoe polish. The paint and polish produced were
tainer and stirred continuously with the addition of good when compared to market ones.
turpentine as the solvent (20.00%) (Chukwumobi,
1987).
REFERENCES
Formulation of shoe polish Ajiwe, V. I. E., Umerie, S. C., Okeke, C. A. & Oburota,
Paraffin wax (20.83%) and beeswax (6.94%) were V. N. (1994). Biores. Technol., 47, 85-6.
melted on a hot plate. Afzelia oil (13.69%) was A.O.C.S. Official Methods (1960). Sampling and Analysis
added with stirring. To this mixture, carbon black of Commercial Fats and Oils. A.O.C.S., Washington, pp.
(2.78%) and turpentine (41-67%) were added. The 801-55.
Boxall, J. & Van Fraunhofer, J. A. (1980). Pain Formula-
liquid was transferred to a container, where it solidi- tion, 1st edn. New York, pp. 4-6.
fied after cooling. Chukwumobi, L. U. (1987). Paint Making. A Report of
Industrial Training Work at Phina Paints Industries. Dept.
of Science Technology, Nnamdi Azikiwe University,
RESULTS AND DISCUSSION Nigeria.
Keay, R. W. J., Onochie, C. F. A. & Stanfield, D. P.
The Afzelia oil obtained after extraction was light (1964). Trees of Nigeria. Clarendon Press, Oxford, pp.
yellow in colour. It did not solidify at room tem- 204-5, 214-8, 300-2.
perature. The percentage oil content and the Lambert, J. & Muir, J. A. (1968). Practical Chemistry, 2nd
physico-chemical properties are shown in Table 1. edn. Heinemann Education Books, London, pp. 315-8.
The percentage oil content is quite high when Norris, F. A. (1965). Fats and fatty acids. In Kirk-Othmer
Encyclopaedia of Chemical Technology, Vol. 8, 2nd edn.
compared to other oil seeds, such as soya bean John Wiley, New York, pp. 770-811.
(16-25), cotton seed (18-28) and rubber seed Williams, K. A. (1966). Oils, Fats and Fatty Foods, 4th edn.
(21-25) (Norris, 1965). This suggests that the pro- Elsevier, New York, pp. 88-122.
cessing of the oil from the seed should be quite
economical and solvent extraction is recommended
as the best extraction method. The oil had a low V. I. E. Ajiwe,* C. A. Okeke &
saponification value but a high iodine value. The low H. U. Agbo
saponification value showed that the oil is a good Nnamdi Azikiwe University, P.M.B. 5025, Awka,
edible oil. This may be the reason why it is accept- Nigeria
able as a soup thickener (Keay et al., 1964). The low
saponification value is directly related to the mean (Received 20 October 1994, revised version received
molecular mass. The iodine value of the oil places it 25 February 1995; accepted 19 March 1995)
within the range of dehydrated castor-bean oil and it