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BISCUITS
SARAH IZHAR
ENROLMENT NO: 2017-335-024, FINAL YEAR, 8th SEMESTER
B.TECH FOOD TECHNOLOGY
► Moisture
► Ash
► Fat
► Protein
► Carbohydrate and
► Energy
MATERIALS & METHOD FOR ANALYSIS OF
WHOLE WHEAT BISCUIT AND RAGI BISCUIT
❑ METHOD:
• Dry a dish with lid in the oven maintained at 100+2ºC.
• Cool the dish in the desiccator.
• Weigh the empty dish and then weigh 5g of sample.
• Heat it in the Hot Air oven for 2 hours.
• Take it out. Cool it in desiccator for 15 minutes.
• Weigh the dish
HOT AIR OVEN DESSICATOR
2. Ash Content (Dry Ashing method)
❑ METHOD:
• Add 3g of sample in previously dried and weighed crucible.
• Heat it over burner or hot plate and then heat it in muffle furnace
(550ºC).
• For about 5 hrs the process will run over.
• Cool the crucible in the desiccator .
• Weigh the sample and calculate the values.
MUFFLE FURNACE
3. Fat estimation (Soxhlet Apparatus)
❑ METHOD:
• Dry a Soxhlet beaker.
• Take a filter paper and weigh 2 gm of sample in it and fold it well.
• In a thimble put cotton and then the folded sample.
• Close it with another cotton ball.
• Put thimble in beaker.
• Add petroleum ether and place it in the assembly.
• PV1= 80°C for 2 hrs and PV2= 180°C for drying of petroleum ether.
• Cool the beaker in dessicator.
• Weigh it.
SOXHLET APPARATUS
4. Protein Estimation (Kjeldhal method)
❑ METHOD:
• Weigh about 0.2 to 0.3g of sample in butter paper.
• Transfer the sample along with butter paper in digestion tube.
• Add 4 g of digestive mixture.
• Add 10 ml of H2SO4.
• Set the digestion unit
• Start digestion for 2:30 hours.
• Cool the digestion tubes.
• Add 30 ml of distilled water.
• Set the distillation unit.
• Add 4% boric acid in conical flask for few seconds to absorb
ammonia.
• Add 40% of alkali in the tube to neutralise the sample.
• After distillation take the conical flask from the unit and
titrations with 0.1N HCL.
• End point is pink in colour.
• Take blank value for calculation.
PROTEIN ASSEMBLY
5. Dietary Fibre
❑ METHOD:
• Weigh duplicate test portion of sample.
• Sample with more than 10% fat needs to be defatted by petroleum
ether.
• Prepare the samples for digestion.
1. α-Amylase: Gelatinize
⮚ Add phosphate buffer (ph 6.0 , 50 ml) in the sample.
⮚ Adjust to ph 6.0 +- 0.2
⮚ Add enzyme
⮚ Incubate at 95-100°C for 30 min in water bath.
2. Protease: Removes protein
⮚ Cool at room temperature.
⮚ Adjust PH to 7.5 +- 0.2.
⮚ Add enzyme and incubate at 60°C for 30 minutes.
❑ METHOD:
• Weigh 1 g of sample.
• Transfer the sample in oven dried Gooch crucible.
• Place the crucible into metal adopter of fibre plus hot extraction unit and
set properly into it.
• Pour 150 ml of 1.25% H2SO4 in it.
• Open the inlet tap water for FIBRA PLUS condensation the switch on
instrument & press RUN key.
• Wait until process completes.
• Open all knobs to drain the solution from extraction unit.
• After draining the acid solution wash the sample with distilled
water twice or thrice.
• Now pour 150 ml of 1.25% NaOH into the extractors from the top.
• Switch on instrument and press RUN key.
• Wait till the process completes.
• Now drain the solution and rinse the sample twice or thrice with
distilled water.
• Now, place the crucibles in hot air oven for drying.
• After drying cool them in Dessicator and weigh them.
• Put the crucible in muffle furnace for ashing.
• Then again cool it in Dessicator and take the final weight.
CRUDE FIBRE ASSEMBLY
RESULTS AND DISCUSSION
▪ Energy
Carbohydrate 69.24%
69.94%