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Pongamia oil

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Pongamia oil is derived from the seeds of theMillettia pinnata tree, which is native to tropical and temperateAsia.Millettia pinnata, also known asPongamia pinnata orPongamia glabra, is common throughout Asia and thus has many different names in different languages, many of which have come to be used in English to describe the seed oil derived fromM. pinnata;Pongamia is often used as the generic name for the tree and is derived from the genus the tree was originally placed in.[1] Other names for this oil includehonge oil,kanuga oil,karanja oil, andpungai oil.

Cultivation

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Pods and seeds ofMillettia pinnata

Millettia pinnata is native toSouth andSoutheast Asia. Typically, the plant starts yielding pods from the fifth year on with the yields increasing each year until it stabilizes around the tenth year. Seeds are usually harvested in the spring, each seed weighing from about 1.1 grams (0.039 oz) to 1.8 grams (0.063 oz). The yield per tree can range from about 10 kilograms (22 lb) to more than 50 kilograms (110 lb) depending on conditions, with an average of 1500-1700 seeds per kilogram. Historically, the pods are removed from the trees by beating the branches with sticks anddecorticated using mallets or stones. Research is ongoing into mechanical harvesting methods.

The basic nutritional components ofMillettia pinnata seeds may change depending on the season and maturity of the tree (table).[2]

ComponentPercentage
Oil27% - 39%
Protein17% - 37%
Starch6% - 7%
Crude fiber5% - 7%
Moisture15% - 20%
Ash2% - 3%

Description

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Pongamia oil is extracted from the seeds byexpeller pressing, cold pressing, orsolvent extraction. The oil is yellowish-orange to brown in color. It has a high content oftriglycerides, and its disagreeable taste and odor are due to bitterflavonoid constituents includingkaranjin, pongamol,tannin andkaranjachromene.[2]

Millettia pinnata has a number of different varieties but little research has been published on the differences between them.[3] This combined with variances in soil and weather can change the specific composition of pongamia oil. Pongamia oil is composed of the followingfatty acids:[2][4]

Fatty acidNomenclaturePercentage
PalmiticC16:03.7% – 7.9%
StearicC18:02.4% – 8.9%
OleicC18:144.5% – 71.3%
LinoleicC18:210.8% – 18.3%
LinolenicC18:32.6%
ArachidicC20:02.2% – 4.7%
EicosenoicC20:19.5% – 12.4%
BehenicC22:04.2% – 5.3%
LignocericC24:01.1% – 3.5%

The physical properties of crude pongamia oil are as follows:[4]

PropertyUnitValue
Acid valuemg KOH/g4.0 - 12
Calorific valuekcal/kg8742
Cetane number42
Densityg/cm30.924
Iodine valueg/100 g86.5 - 87
Saponification valuemg KOH/g184 - 187
Specific gravity0.925
Unsaponifiable matter% w/w2.6 - 2.9
Viscositymm2/sec40.2
Boiling point°C316
Cloud point°C3.5
Fire Point°C230
Flash point°C225
Pour point°C-3.0

Uses

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Traditional

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It has been used aslamp oil, inleather tanning, insoap making, and as alubricant for thousands of years. Its toxicity, as well as its color, bitter taste, and disagreeable odour, keep it from being used in cooking, but it does have uses in traditional medicine for treating skin disease and liver disease.[1]

It is used as a fish poison, as the metabolites karanjin and pongamol are both toxic to fish.[5]

Biodiesel

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Many studies have been done to convert pongamia oil intobiodiesel.[4][6][7][8][9] The following table shows the physical properties of the methyl esters of pongamia oil versus the ASTM D6751 andEN 14214 biodiesel standards:

PropertyUnitMethyl estersASTM D6751EN 14214
Acid valuemg KOH/g0.46 - 0.5<0.8<0.5
Caloric valuekcal/kg3700
Cetane Number41.7 - 56>45>51
Density at 15 °Cg/cm30.86 - 0.880.87 - 0.890.86 - 0.90
Viscosity at 40 °Cmm2/s4.771.9 - 6.03.5 - 5.0
Iodine valueg/100 g86.5 - 91<120
Oxidation Stability at 110 °Ch2.24>6
Saponification valuemg KOH/g184 - 187
Unsaponifiable matter% w/w2.6 - 2.9
Boiling point°C316
Cloud point°C190/-15 †
Fire Point°C230
Flash point°C174>130>101
Pour point°C15
† This is not a property of the EN 14214 standard; it is country specific standard for summer/winter seasons.

The comparison of themethyl esters of pongamia oil to the ASTM D6751 standard for biodiesel fuels shows that processed pongamia oil is within the standards. Research has shown thatjatropha or pongamia oil can be mixed withpalm oil to achieve an improved low-temperatureviscosity than pure palm oil and a higher oxidation stability than pure jatropha or pongamia oil. In addition, the methyl esters of pongamia oil have a cloud point of 19 °C, which is outside some country specific standards, and a pour point of 15 °C both of which would be problematic in lower temperature climates.

See also

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References

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  1. ^ab"Pongamia Factsheet"(PDF). Retrieved2013-10-02.
  2. ^abc"Factsheet forPongamia pinnata (L.) Pierre". New Crops at Purdue University. 8 January 1998. Retrieved2 September 2025.
  3. ^"Weed Risk Assessment : Pongamia"(PDF). Daff.qld.gov.au. Retrieved2013-11-21.
  4. ^abcAshok Pandey (2008).Handbook of Plant-Based Biofuels. CRC. pp. 255–266.ISBN 978-1-56022-175-3.
  5. ^S., Mahli, S.; P., Basu, S.; P., Sinha, K.; C., Banerjee, N."Pharmacological effects of karanjin and pongamol [from seed oil of Pongamia pinnata]".www.cabdirect.org. Retrieved2016-03-03.{{cite web}}: CS1 maint: multiple names: authors list (link)
  6. ^Meher, L C; Naik, S N; Das, L M (November 2004)."Methanolysis of Pongamia pinnata (karanja) oil for production of biodiesel"(PDF).Journal of Scientific & Industrial Research.63:913–918.
  7. ^Karmee, Sanjib Kumar; Chadha, Anju (September 2005). "Preparation of biodiesel from crude oil of Pongamia pinnata".Bioresour. Technol.96 (13):1425–9.doi:10.1016/j.biortech.2004.12.011.PMID 15939268.
  8. ^Moser, Bryan R. (2009)."Biodiesel production, properties, and feedstocks"(PDF).In Vitro Cellular & Developmental Biology - Plant.46 (3):229–266.doi:10.1007/s11627-009-9204-z.S2CID 8730735.
  9. ^Mathiyazhagan, M.; Ganapathi, A.; Jaganath, B.; Renganayaki, N.; Sasireka, N. (April 2011)."Production of Biodiesel from Non-edible plant oils having high FFA content".International Journal of Chemical and Environmental Engineering.2 (2):119–122.
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