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Food Analysis Practical Manual
Food Analysis Practical Manual
Aim- To determine the moisture content in food (Using hot air oven).
Principle- Moisture content is important for shelf-life and storage. Very high moisture
content (greater than 14.5%) attracts mold, bacteria, and insects, all of
which can result in storage issues or baking quality deterioration.
Procedure:
1 : Weigh an empty dry Aluminum dish / Petri Dish and note the weight as (W1).
2 : Take 5-10gm of sample in dish and weight again note the weight as (W2).
3 : Transfer in oven at 1050 C temperature for 2 hrs or till the weight becomes constant.
4 : Take out dish and transfer the sample in a desiccator for cooling and weight again (W3).
Result-
Conclusion /
Discussion
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Rayat Shikshan Sanstha’s
Karmaveer Bhaurao Patil College, Vashi.
Food Technology
PRACTICAL MANUAL
Procedure:
Weigh 10 g of sample (Remove moisture from the oil seed by keeping in oven at 1300 0 C for 10-
1 :
20 min) and transfer it into the thimble (small pouch).
2 : Close the thimble with cotton and transfer the tube in Soxhlet apparatus.
3 : Add sufficient volume of solvent into the round bottom flask (150 ml).
Remove the flask and evaporate the solvent by keeping it in oven or water bath (No direct
7 :
heat).
Result-
Conclusion /
Discussion
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Rayat Shikshan Sanstha’s
Karmaveer Bhaurao Patil College, Vashi.
Food Technology
PRACTICAL MANUAL
Principle- Ash is an inorganic material left after the destruction of organic material
completely present in the food. Ash is a measure of mineral content and is used
to grade flour into different varieties.
Procedure:
1 : Weigh an empty dry Silica dish and note the weight.
3 : Keep the dish in muffle furnace; at 6000 C until the clean ash is obtained (It takes 5-8 hrs).
4 : Take out the dish from furnace, cool it in desiccator and take the weight.
Result-
Conclusion /
Discussion
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Principle- The crude fiber content is commonly used to measure nutritive value of
food product to detect quality and quantity of adulteration. The crude fiber
consists largely of cellulose and lignin (97%) and some mineral materials. It
represents only 60-80% of cellulose and 4-6 % of lignin. During the acid and
alkaline hydrolysis oxidative hydrolytic degradation of cellulose and in some
amount of lignin is carried out. The residue obtained after final filtration is
weighed, incinerated, cooled and weighed again. The loss in weight gives
the crude fiber content.
Procedure:
Extract 2gm of sample, smash it and then add 20ml petroleum ether or ether in conical
1 : flask to remove fat for 30mins (Initial boiling temperature 35-38ºC and final temperature
of 52ºC.)
Boil the dried sample (crude fat free sample) with 200ml of 0.0255 N H 2SO4 for 30mins
2 :
with bumping chips.
3 : Filter through muslin cloth and wash with boiling water until washings are free from acid.
4 : Check the acid wash drain with pH litmus paper to confirm washing end point (pH-7).
6 : Filter through the muslin cloth and wash with 25ml of boiling H 2SO4 and 25ml of alcohol
(50% concentration).
8 : Dry the residue for 2hours at 130ºC and cool it in desiccators and pre-weight (W 2).
9 : Ignite for 30mins at 600º C in muffle furnace, cool and weigh (W 3).
Calculations-
Percent crude fiber content = Loss in weight on ignition (W2 - W1) - (W3 - W1) X 100
Weight of sample
Result-
Conclusion /
Discussion
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