food chemistry and nutrition practical manual · 03/08/2015 · food chemistry and nutrition-...

FOOD CHEMISTRY

AND NUTRITION- PRACTICAL

MANUAL

©Vedpal Yadav, Lecturer in Food Technology, Government Polytechnic, Mandi Adampur, Hisar,

Haryana, India-125052. e-mail- [email protected] Mobile- +919416589819

mailto:[email protected]

3.2 FOOD CHEMISTRY & NUTRITION L T P 3 - 2

LIST OF PRACTICALS 1. Determination of moisture in a given food sample

2. Determination of protein in a given food sample

3. Determination of carbohydrates in a given food sample

4. Determination of ash in a given food sample

5. Determination of fat in a given food sample

6. Determination of pH of a given sample

7. Determination of acidity of given food sample/beverage

8. Determination of total non reducing and reducing sugars

9. Determination of vitamin C in given food sample

10. Determination of diastase enzyme activity

11. Identification of pigments in a given food sample

12. Effect of Baking Soda in CO2 production

13. Detection of Saccharine in beverages

14. Visit to hospital/slide show on various nutritional deficiency disorders

©Vedpal Yadav, Lecturer in Food Technology, Government Polytechnic, Mandi Adampur, Hisar, Haryana, India-125052. e-mail- [email protected] Mobile- +919416589819 Last Updated- 28 September 2016

Food Chemistry and Nutrition- Practical Manual

3

Table of Contents

Experiment Page No. Signature

Experiment- 1- Moisture Content- Lab Oven Method 4

Experiment- 2- Moisture Content- Using Moisture Meter 7

Experiment- 3- Ash - Total 10

Experiment- 4- Ash- Acid Insoluble 14

Experiment- 5- Crude Protein- Kjeldahl Method 17

Experiment- 6- Crude Protein- Protein by Kjeltec 24

Experiment- 7- Crude Fat- Soxhlet Apparatus Method 29

Experiment- 8- Total Carbohydrates 33

Experiment- 9- Crude Fiber 35

Experiment- 10- Determination of pH using pH paper and Universal Indicator 37

Experiment- 11- Determination of pH using pH Meter 44

Experiment- 12- Determination of acidity of given honey sample 54

Experiment- 13- Determination of acidity of extracted fat in a given sample of biscuit 57

Experiment- 14- Determination of reducing and non- reducing sugars in a given food sample

59

Experiment- 15- Determination of Vitamin- C (Ascorbic Acid) in a given food sample 62

Experiment- 16- Determination of Diastase enzyme (α- amylase) activity in a given food sample by Falling Number test

65

Experiment- 17- Identification of pigments in a given food sample by paper chromatography

68

Experiment- 18- Effect of Baking Soda in CO2 production 72

Experiment- 19- Detection of Saccharine in beverages 74

Experiment- 20- Visit to hospital/slide show on various nutritional deficiency disorders 76



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Experiment- 1- Moisture Content- Lab Oven Method

Objective: To find out the moisture content from a given food sample by lab oven method. Theory: Upon heating water evaporates and loss of weight is equal to the moisture content of material. Materials:

1. Enough food sampleto supply three 20 gram samples. 2. Oven (almost any oven will do, provided the temperature can be set reliably at 130°C for an

extended period of time). 3. Analytical Balance. 4. Tray (to place the paddy grain samples on before drying in the oven). 5. Simple plastic containers or small paper bags to hold grain. 6. Pen/pencil, paper and calculator to compute the average of three samples and record the

moisture content. Procedure:

1. Set the oven temperature to 130°C. 2. From your paddy grain supply, use your scale to measure three 20-gram paddy grain samples. 3. Place the three samples inside the oven and leave for 16-24 hours. 4. Measure the final weight of each sample after the 16 to 24 hours. 5. Compute the moisture content for each sample using the equation. 6. You now have three separate moisture content results. Compute the average of these results by

adding them together and dividing by 3. Calculation:

Moisture Content (%) = {(W2 – W1) / (W1 – W)} x 100 Where, W = Weight of empty moisture dish W1 = Weight of empty moisture dish + Sample W2 = Weight of empty moisture dish + Dried Sample Observations:

Sample Name

Wheat Flour

Sample Number

Weight of Empty Moisture Dish (W)

(in gms.)

Weight of Moisture

Dish+Sample (W1) (in gms.)

Weight of Moisture Dish+Dried Sample

(W2) (in gms.)



5

Sample Number


(in gms.)

Weight of Moisture



(W2) (in gms.)

Weight of Sample (W1-W) (in gms.)

Weight of Moisture (W2-W1)

(in gms.) Moisture % Average Moisture %

% RSD

Conclusions:

1. Did each of your samples contain approximately the same amount of moisture content? 2. What was the average moisture of all three samples? 3. Based on what you know about correct moisture content for milling (14%), is the paddy rice you

sampled ready for milling? Why or why not?

Sample Name

Wheat Flour

Sample Number


(in gms.)

Weight of Moisture



(W2) (in gms.)

A 34.5679 39.6384 39.5173

B 34.3369 39.7865 39.6652

C 34.1256 39.5596 39.4396


Weight of Moisture (W2-W1)

(in gms.) Moisture % Average Moisture %

% RSD

5.0705 0.1211 2.39

2.28 4.327 5.4496 0.1213 2.23

5.4340 0.1200 2.21



6

Space for Observations and Calculations



7

Experiment- 2- Moisture Content- Using Moisture Meter

Objective: To find out the moisture content from a given sample by using moisture meter. Materials:

1. Moisture meter and instructions for use 2. Paddy rice – enough to provide three samples for the moisture meter (approximately one handful) 3. Simple plastic containers or small paper bags to hold grain 4. Pen/pencil, paper and calculator to compute the average of three samples and record the moisture

content Procedure:

1. Read the operator’s instructions. 2. Turn the moisture meter on. 3. Ensure the machine is set for paddy rice. 4. Fill the tray or bowl of the moisture tester with a sample of the paddy rice to be tested 5. Turn or press the knob until the moisture reading is displayed. 6. Test at least three samples and calculate the average of the three readings.

Observations & Calculations:

Sample

Volume

Thickness

Sample No. Moisture %

Average Moisture Content

% RSD

Conclusions:

1. Did each of your samples contain approximately the same amount of moisture content? 2. What was the average moisture content of all three samples? 3. Is the paddy rice you sampled ready for milling? Why or why not?



8

Sample Paddy

Volume C

Thickness 3.25

Sample No. Moisture %

1 10.30

2 10.40

3 10.80

Average Moisture Content 10.50

% RSD 2.52



9




10

Experiment- 3- Ash - Total

Objective: To find out the ash in the given food sample. Theory: Organic matter is burnt off at as low temperature as possible. Heating is done in stages, first to char the product thoroughly and finally to ash at 550° C in a muffle furnace. The inorganic matter left after burning organic matter is cooled and weighed. Apparatus:

1. Crucible 2. Heating Plate 3. Muffle Furnace 4. Dessicator 5. Analytical Balance

Procedure:

1. Place the crucibles in muffle furnace to heat at 550° C for 15 minutes. 2. Remove the crucibles, cool in a dessicator for one hour and weigh the crucible (W). 3. Weigh 2 g of sample in the crucible (W1). 4. Keep the sample on a hot plate till smoking ceases and sample become thoroughly

charred. 5. Place the crucibles inside the muffle furnace and heat to 550° C for 5 to 6 hours. 6. Let the furnace cool and take out crucibles containing ash, clean and white in

appearance. 7. If traces of carbon are still evident, cool the crucible, add 1 – 2 ml of water and stir with

a glass rod to break up the ash. Dry on steam bath and place in muffle furnace and again heat at 550° C.

8. Cool the crucible in a dessicator and reweigh (W2) the crucible containing ash. Calculation: Ash % = {(W2 – W) / (W1 – W)} x 100 Where, W = Weight of empty crucible W1 = Weight of empty crucible + Sample W2 = Weight of empty crucible + Ashed Sample Observations:

Sample Name ___________________________

Sample Number

Weight of Empty Silica Crucible (W)

(in gms.)

Weight of Silica Crucible+Sample

(W1) (in gms.)

Weight of Silica Crucible+Ashed Sample

(W2) (in gms.)



11

Sample Number


(in gms.)


(W1) (in gms.)


(W2) (in gms.)


Weight of Ash (W2-W) (in gms.)

Ash % Average Ash % %

RSD



12

Sample Name Wheat Flour

Sample Number


(in gms.)


(W1) (in gms.)


(W2) (in gms.)

A 10.2569 12.2698 10.2762

B 10.2444 12.3009 10.2642

C 10.3597 12.4001 10.3801

Weight of

Sample (W1-W) (in gms.)

Weight of Ash (W2-W) (in gms.)

Ash % Average Ash % %

RSD

2.0129 0.0193 0.96

0.97 2.381 2.0565 0.0198 0.96

2.0404 0.0204 1.00



13




14

Experiment- 4- Ash- Acid Insoluble

Objective: To find out the acid insoluble ash from a given food sample. Reagents: Dil HCL approximately 0.5 N prepared from conc.HCl Procedure: To the ash contained in a dish, add 25 ml of dil, HCl. Cover with a watch glass and heat on a water bath for 10 minutes. Allow to cool and fitter the contents of the dish through a Watman filter paper No.42 or its equivalent. Wash the filter paper with water until the washing are free from the acid and return it to the dish. Keep it in an electric oven maintained at 135 ± 20C for about 3 hrs. Ignite in a muffle furnace at 550-6000C for 1hr. Cool the dish in a dessicator and weigh. Repeat the process of igniting in muffle furnace, cooling and weighing at half hours interval until the difference in mass between 2 successive weighings is less than 1 mg. Note: the lowest mass. Calculation % Ash Insoluble ash (on dry basis)

% by mass =

)WW(

)WW(100

1

2

Where W2 - Mass in g of dish + acid insoluble W - Mass in g of empty dish W1 - Mass in g of dish with the dried material Observation and Result Acid insoluble ash % of a given sample

)7786.377786.45(

)7786.377816.37(100

=%037.0

8

0030.0100

Where W2 = 37.7816 g W1 = 45.7786 g W = 37.7786 g



15

Sample Name

Wheat Flour

Sample Number

Weight of Empty Silica Crucible (W) (in gms.)


(W1) (in gms.)

Weight of Silica Crucible+Acid Insoluble Ashed Sample (W2)

(in gms.) A 10.2569 12.2698 10.2641

B 10.2444 12.3009 10.2521

C 10.3597 12.4001 10.3671

Weight of

Sample (W1-W) (in gms.)

Weight of Acid Insoluble Ash (W2-W)

(in gms.)

Acid Insoluble Ash %

Average Acid Insoluble Ash % % RSD

2.0129 0.0072 0.36

0.36 1.604 2.0565 0.0077 0.37

2.0404 0.0074 0.36



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17

Experiment- 5- Crude Protein- Kjeldahl Method

Objective: To find out the amount of crude protein in a given food sample. Introduction The protein content of foods can be determined by numerous methods. The Kjeldahl, nitrogen combustion (Dumas) and infrared spectroscopy methods for protein analysis are based on nitrogen determination. The methods are from the Official Methods of Analysis of AOAC International (1), and are used commonly in research laboratories working on proteins. Theory Nitrogen is one of the five major elements found in organic materials such as protein. This fact was recognized by a Danish chemist, Johan Kjeldahl, who used it as a method of determining the amount of protein in samples taken from a wide variety of organisms. In 1883 Kjeldahl presented to the Danish Chemical Society a method (much revised since his day) for determining the amount of nitrogen in mixtures of substances containing ammonium salts, nitrate, or organic nitrogen compounds. The central basis used in this procedure is the oxidation of the organic compound using strong sulfuric acid. As the organic material is oxidized the carbon it contains is converted to carbon dioxide and the hydrogen is converted into water. The nitrogen, from the amine groups found in the peptide bonds of the polypeptide chains, is converted to ammonium ion, which dissolves in the oxidizing solution, and can later be converted to ammonia gas.

The Kjeldahl method of nitrogen analysis is the worldwide standard for calculating the protein content in a wide variety of materials ranging from human and animal food, fertilizer, waste water and fossil fules.

Figure 1 Trapping the Ammonia

Principle The Kjeldahl procedure can be basically divided into three parts: (1) digestion, (2) distillation, (3) titration. In the digestion step, organic nitrogen is converted to an ammonium in the presence of a catalyst at approximately 370ºC. In this experiment, the sample is digested in H2SO4, using Copper-based catalyst, converting N to NH3 which is distilled and titrated.

Protein (NH4)2SO4

Sulfuric acid

Heat, catalyst



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In the distillation step the digested sample is made alkaline with NaOH and the nitrogen is distilled off as NH3. This NH3 is trapped in a boric acid solution. The amount of ammonia nitrogen in this solution is quantified by titration with a standard HCl solution. A reagent blank is carried through the analysis and the volume of HCl titrant required for this blank is subtracted from each determination. This analysis determines total nitrogen and not usable nitrogen and this is the reason it is called a crude protein analysis.

A three step procedure The Kjeldahl method consists of three steps, which have to be carefully carried out in sequence:

1. the sample is first digested in strong sulfuric acid in the presence of a catalyst, which helps in the conversion of the amine nitrogen to ammonium ions,

2. the ammonium ions are then converted into ammonia gas, heated and distilled. The ammonia gas is led into a trapping solution where it dissolves and becomes an ammonium ion once again,

3. finally the amount of the ammonia that has been trapped is determined by titration with a standard solution, and a calculation made.

Figure 2 Digetion

Step One: Digestion of the Sample This is the most time-consuming step in the analysis. The purpose of this step is to break down the bonds that hold the polypeptides together, and convert them to simpler chemicals such as water, carbon dioxide and, of course, ammonia. Such reactions can be considerably speeded up by the presence of a catalyst and by a neutral substance, such as potassium sulfate (K2SO4), which raises the boiling point of the digesting acid and thus the temperature of the reaction. Catalysts are also used to help in the digestion process; many different one have been tried including selenium, mercury, copper, or ions of mercury or copper.

(NH4)2SO4 + 2NaOH 2NH3 + Na2SO4 + 2H2O NH3 + H3BO3 (boric acid) NH4 + H2BO3

-

(borate ion)

H2BO3

- + H+ H3BO3



19

Figure 3 Digestion by Sulfuric Acid and Heat

Digestion is accomplished by:

1. Weighing out approximately 1 gm of the sample containing protein, making a note of the weight, and placing the sample into a digestion flask, along with 12-15 ml of concentrated sulfuric acid (H2SO4).

2. Adding seven grams of potassium sulfate and a catalyst, usually copper. 3. Bringing the digestion tube/flask and mixture to a "rolling boil" (about 370oC to 400oC) using a

heating a block. 4. Heating the mixture in the tube/flask until white fumes can be seen, and then continuing the heating

for about 60-90 mins. 5. Cooling the tube/flask and cautiously adding 250 mls of water.

Step Two: Distillation The purpose of the next step, distillation, is to separate the ammonia (that is, the nitrogen) from the digestion mixture. This is done by,

1. raising the pH of the mixture using sodium hydroxide (45% NaOH solution). This has the effect of changing the ammonium (NH4

+) ions (which are dissolved in the liquid) to ammonia (NH3), which is a gas.

2. separating the nitrogen away from the digestion mixture by distilling the ammonia (converting it to a volatile gas, by raising the temperature to boiling point) and then trapping the distilled vapors in a special trapping solution of about 15 ml HCl (hydrochloric acid) in 70 ml of water.

3. removing the trapping flask and rinsing the condenser with water so as to make sure that all the ammonia has been dissolved.

Figure 4 Trapping of Ammonia

Step Three: Titration As the ammonia dissolves in the acid trapping solution, it neutralizes some of the HCl it finds there. What acid is left can then be "back titrated", that is titrated with a standard, known solution of base (usually NaOH). In this way the amount of ammonia distilled off from the digestive solution can be calculated, and hence the amount of nitrogen in the protein determined.



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Figure 5 Titration

The quantities of acid, and hence ammonia are determined by,

1. adding an indicator dye to the acid/ammonia trapping solution. This dye should turn a strong color, indicating that a significant amount of the original trapping acid is still present.

2. putting a standard solution of NaOH (sodium hydroxide) into the buret (a long tube with a tap at the end), and slowly, slowly adding small amounts of the sodium hydroxide solution to the acid solution with the dye.

3. watching for the point at which the dye turns orange, indicating that the "endpoint" has been reached and that now all the acid has been neutralized by the base.

4. recording the volume of the neutralizing base (sodium hydroxide solution) that was necessary to reach the endoint.

5. performing a calculation to find the amount of ammonia, and thus nitrogen, that came from the original sample.

Calculations One mole of ammonia coming from the digestion mixture (and hence from the original protein) will neutralize exactly one mole of the acid in the trapping flask. The first calculation, therefore, is to find the number of moles of ammonia that have been produced and then trapped from your sample(s). This is done by,

calculating the number of moles of acid in the trapping flask originally (before any ammonia was trapped) by multiplying the molarity of the acid solution by the volume of the trapping solution

moles of acid =molarity of acid x volume used in flask (molesA = M x V)

calculating the number of moles of base (NaOH) that were added from the buret to neutralize the remaining acid (that NOT neutralized by the ammonia).

moles of base =molarity of base x volume added from buret (molesB = M x V)

subtracting the "moles of base" added from the "moles of acid" present at the beginning, to get, the number of "moles of ammonia" coming from the protein, the number of "moles of ammonia" is the same as the "moles of nitrogen", so ... to calculate the number of grams of nitrogen in the original sample of protein, multiply the

"moles of nitrogen" by the atomic mass of nitrogen (mass of atoms of nitrogen), gms nitrogen =moles nitrogen x atomic mass (gN = molesN x 14.0067)



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Figure 6 Calculation

Percent Nitrogen The percentage of nitrogen found in the orginal sample can now be calculated by: %nitrogen =(gms nitrogen / gms sample) x 100 %N = (gN / gS) x 100 It is also possible to calculate the amount of crude protein in the sample. Although there are differences between different samples, the amount of "crude protein" (CP) can be found by multipling the percent Nitrogen by a factor (usually 6.25). CP = %N x 6.25 Weight of food sample = W1 Volume of acid in sample titration = V1 Volume of acid in blank titration = BL Concentration of acid, M = 0.1 M See below for calculation of total and percentage values

Total Nitrogen and Protein in the food, measured in dry sample: Total Nitrogen = (V1 – BL) x 0.1 x 0.0014 x Total Dry Matter of Food W1 where 0.1 is molar concentration of the HCl and 0.0014 is factor for equivalence of HCl to NH3

To convert to protein multiply by the appropriate factor:



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x 6.25 for meat and general protein x 6.38 for milk protein x 5.70 for cereal protein. NB These are not perfect and you must choose according to the major type of food in the sample. In most cases this will be the first one.

Percentage Nitrogen and Protein In original, wet sample: Nitrogen, % = (V1 – BL) x 0.1 x 0.0014 x 100 x %Dry Matter W1 100 To convert to protein multiply by the appropriate factor: x 6.25 for meat and general protein x 6.38 for milk protein x 5.70 for cereal protein. NB These are not perfect and you must choose according to the major type of food in the sample. In most cases this will be the first one.



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24

Experiment- 6- Crude Protein- Protein by Kjeltec

Principle All nitrogen in the sample is converted to NH4

+ by digestion with concentrated H2SO4 and H2O2 using inorganic salt catalysts at a high temperature. The solution is then made alkaline (with NaOH) and steam is passed through and the ammonia is distilled into a solution of boric acid that contains an indicator (methyl orange). Finally the distilled ammonia, now dissolved in the boric acid, is titrated against 0.1 M HCl. The Kjeldahl method described above is the standard method for determining protein content. The Kjeltec is a semi-automated version of this method. Apparatus/Instrument/Chemicals/Samples

Sulfuric acid 98% min.

Catalyst tablets to be used: Kjeltabs CX

Caustic soda 32%

Boric acid solution 2%

Indicator Solution M5 (Merck) or similar

Standard acid 0.1N or c = 0.1 mol/, alternatively sulfuric acid 0.1N or c = 0.05 mol/l

Mechanical comminuting instrument

Analytical balance (0.001 g)

Kjeldahl digestion block Kjeldatherm, Turbotherm, flask heater for Kjeldahl flask with wide neck opening

Vapodest distillation System

Burette, 50 ml nominal capacity, with a scale on 0.05 ml or titration system (not with the Vap 50) or pH meter with combined electrode

1 Digestion Wear Gloves and Safety Glasses throughout this Procedure

1. Collect two Kjeldahl digestion tubes and label them with a permanent marker close to the top. Always carry them in a tube rack (share with your colleagues).

2. Accurately weigh out (to nearest mg) in duplicate approximately 0.1 g of dry sample on to a filter paper (W1).

3. If using a wet sample, pipette about 1 g (to nearest mg) directly into the bottom of a labelled digestion tube.

4. Fold up the paper containing the dry sample and carefully transfer the whole parcel to a labelled digestion tube.

5. Place a filter paper in a further digestion tube to act as a blank. 6. Add 2 catalyst tablets (copper sulphate + potassium sulphate) to each tube. Then add 10 cm3

concentrated H2SO4 and mix by gentle swirling. Take care. See the demonstrator before making these additions.

7. Now add 10 cm3 H2O2 in a fume cupboard and beware of frothing. Add the peroxide slowly at first. 8. Place the tubes in the digestion block and digest until clear (30 minutes to 2 hours). Check that there

are no black carbon particles visible. 9. Allow the tubes to cool until barely warm but still liquid. Then add approximately 70 cm3 distilled

water.



25

CARE - add the water slowly in the early stages and beware of spitting. If necessary the digestion tubes may be left at this stage by covering the top of the tubes with Parafilm.

2 Distillation and Titration a) In turn place the tubes into the distillation unit and twist to seal. If this is not done properly the tube

contents may leak out and the results be useless. b) Close the door on the apparatus and start the cycle. c) The exact sequence will depend on which instrument you are using. d) The apparatus will automatically add alkali to the tube and then bubble steam to distil off the ammonia.

This is collected in boric acid. The Foss Kjeltec machine used boric containing indicator but the Buchi machine measure pH. The titration is automatic. The volume of acid used is displayed on the front of the apparatus. With both instruments the results are saved and can be accessed later if necessary.

e) When the titration is finished the tubes will be emptied automatically. Record the volume of acid used. f) Insert the next tube and continue. Procedure 1. Sample Preparation

1. Weigh accurately 2.00g comminuted sample as a start on a piece of a filter paper. 2. Store the sample air tight so that any changes or decay of the composition is avoided. Prior to the

analysis the sample should be at room temperature. The examination of the thus prepared sample has to be done within the following 24 h.

2. Digestion chemicals

1. The chemicals are added. Sulfuric acid is used to wash down any sample residue, which might remain at the glass walls.

Chemicals Sulfuric acid 20 ml Kjeltabs 2 Indicator solution M5

Standard acid 0.1N or c=0.1mol/L; alternatively sulfuric acid 0.1N or c=0.05mol/L

3. Digestion with Kjeldatherm

When working with a Kjeldatherm-System with 250 ml Kjeldatherm-digestion tubes, the following digestion parameters are recommended:

Time in min Temperature in ° C Comments 40 400 Digestion tubes are put into the preheated block and

time it takes for the sample to become translucent 30 400 Dehydrate the sample

Foaming during the digestion has to be expected, however, the foaming should not go higher then 2/3 of the glass.

If excessive reactions should occur, take out the insert rack.



26

During the digestion black particles remaining at the glass wall are washed back with condensing sulfuric acid.

The sample glass has to be translucent after the digestion in order to obtain good results. 4. Digestion with Turbotherm

When working with a Turbotherm-System with 250 ml Kjeldatherm-digestion tubes, the following program parameter are recommended:

Time in min

Power in % Comment

10 to 15 100 Heating up of the system to bring digestion solution to boiling

60 70 to 80 Digestion solution is turning translucent after ca 20 to 30 min

5. Digestion with Flask heater

For Serial Flask Heater with 500 or 750 ml Kjeldahl flask with wide neck opening the following procedure is recommended:

Time in min

Power Comments

20 3 Heating up till the digestion solution is boiling 50 1,5 After 20-30 min. the sample should turn translucent.

Wash down remaining sample particles with condensing sulfuric acid into the flask.

6. Suction

During the entire digestion period the scrubber should be on. About 1200 ml of a 15% caustic soda is recommended for the washing bottle; this amount is sufficient to neutralize digestion gases of about 60 digestions.

The cooling off period after the lifting of the insert rack or the cooling off period after turning off the heating is about 30 minutes; during this time the scrubber should be working as well.

7. Distillation

After the digested sample has cooled off the water steam distillation is done according to the following program:

Program parameter Vap 50 Water addition in s 9 NaOH addition in s 8 Reaction time in s 0 Distillation time in s 240 Steam output in % 100 Suction sample in s 25 Boric acid addition in s 6 s Suction receiver in s 25 Titration Auto Calculation Auto



27

8. Titration (is done automatically when using the Vap 50)

3 - 4 drops of an indicator mixture M 5 are added to the receiving solution and it is then titrated with 0.1 N titration acid till the color changes from green to grey/violet.

If the determination of the endpoint is done with a pH-meter or a titrator, the addition of the indicator mixture is obsolete.

9. Blank Value

For the determination of the blank value the analysis (digestion and distillation) is run just using the given chemicals.

The consumption of those chemicals has then to be taken into account when the calculation is done.

10. Calculation % N = 1.4007 * c * (V - Vb)

Sample weight (g)

c : Concentration of the standard-acid solution: Hydrochloric acid 0.1N or c = 0.1 mol/l Alternative: sulfuric acid 0.1N or c = 0.05 mol/l V: Consumption of the standard acid in ml (Sample) Vb: Consumption of the standard acid in ml (Blank Sample) % raw protein= % N * 6.25 Nitrogen to Protein Conversion Factors for Various Foods

Product Factor Egg or meat 6.25 Dairy products 6.38 Wheat 5.70 Other cereal grains or oilseeds 6.25 Almonds 5.18 Peanut and Brazil nuts 5.46 Other tree nuts and coconut 5.30 Soybean products 6.08



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29

Experiment- 7- Crude Fat- Soxhlet Apparatus Method

Objective: To find out the amount of crude fat in a given food sample. Principle: A Soxhlet extractor is a piece of laboratory apparatus invented in 1879 by Franz von Soxhlet. It is a procedure to remove lipids (fats) from food. A solvent is used to wash the solid using a reflux apparatus. The sample is dried and ground and placed in a tube above the extraction solvent. When heated, the solvent evaporates into a gas, then cools into a liquid in a condenser. It then leaks into the sample tube. This continues several hours until the lipid is removed from the sample. The solvent is evaporated off, and the amount of lipid is determined. Apparatus

Soxhlet extraction apparatus - A glass Soxhlet extraction apparatus of suitable size (100 mL) for containing the sample and a 250 mL collection flask is required for the conventional Soxhlet procedure. An automated extraction apparatus (Brinkmann Buchi B-810 or equivalent) with circulating oil bath and associated glassware is required for the automated Soxhlet procedure.

Alundum extraction thimbles - Medium porosity (10 - 15 mm pore), sized to fit the Soxhlet extractor.

Analytical balance - Sensitive to 0.1 mg.

Rotary evaporator with vacuum and water bath - Rotary evaporator equipped with a "bump" trap, condenser, receiving vessel, and vacuum source sufficient to pull a vacuum of less than 150 torr.

Vacuum oven or drying oven - Vacuum oven should be controllable to a temperature of 40 ± 1°C and vacuum of between 75 to 100 torr. If drying oven is used in place of the vacuum oven, the drying oven must be able to maintain 45 ± 2°C

Reagents and Materials

Ethyl alcohol, 95% in water (190 proof), USP grade.

Boiling chips.

Glass wool.

Buchner funnel.

Desiccator. Procedure 1. Dry the Soxhlet extraction thimble at 105°C to constant weight. Remove, cool to room temperature in a

desiccator, and weigh to the nearest 0.1 mg. 2. Carefully add the sample to the extraction thimble. Do not overfill the thimble, leave at least a 1 cm gap

between the sample and the top of the thimble. Weigh the filled thimble to the nearest 0.1 mg. Place a plug of glass wool on top of the sample to prevent sample loss during the extraction.

Note: Samples for total solids determination (following Laboratory Analytical Procedure #001, Determination of Total Solids and Moisture in Biomass) must be weighed out at the same time as the samples for the extractives determination. If this determination is done at a later time, an error in the calculation of the amount of extractives will be introduced, since the moisture content of a biomass sample can change rapidly when exposed to air.

3. Place several boiling chips into a clean, dry receiving flask or beaker. Weigh the container, with chips, to the nearest 0.1 mg and record as the tare weight of the container.

4. For a conventional Soxhlet extraction (this procedure was reproduced from the Chemical Technologies Research Branch Procedure #001c, Determination of Extractives Content): 4.1. Assemble the Soxhlet apparatus using at least 160 mL of 95% ethanol. Insert the thimble and heat

at reflux for 24 hours. Periodically check the reflux rate and adjust the heating rate to give four to



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five solvent exchanges per hour in the Soxhlet thimble. Approximately 100-120 solvent exchanges are required during the 24 hour period.

4.2. When the extraction time is complete, remove the thimble and carefully transfer the sample to a Buchner funnel. Remove any residual solvent by vacuum filtration and wash the sample thoroughly with 95% ethanol, collecting all of the filtrate. Allow the biomass to air dry in the Buchner funnel while it is still attached to the vacuum system.

4.3. Combine the filtrate from the previous step and any solvent from the upper section of the Soxhlet apparatus with the solvent in the 250 mL flask. Place the flask on the rotary evaporator and remove the solvent under vacuum. Use a water bath temperature of 45 ± 5°C to heat the flask during evaporation.

4.4. After all of the visible solvent is removed by the rotary evaporator, place the flask in a vacuum oven (75-100 torr) at 40 ± 1°C for 24 ± 1 hour. Remove the flask at this time and allow to cool to room temperature in a desiccator. Weigh the flask and record this total weight to the nearest 0.1 mg.

Figure 7 A schematic representation of a Soxhlet extractor

1: Stirrer bar 2: Still pot (the still pot should not be overfilled and the volume of solvent in the still pot should

be 3 to 4 times the volume of the soxhlet chamber) 3: Distillation path 4: Thimble 5: Solid 6: Siphon top 7: Siphon exit 8: Expansion adapter 9: Condensor 10: Cooling water in 11: Cooling water out

http://en.wikipedia.org/wiki/File:Soxhlet_extractor.svg



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Figure 8 Mechanism of Soxhlet extractor

Calculations 1. Calculate the oven dry weight of the sample, using the average total solids content.

2. Calculate the amount of extractives in the sample, on a percent dry weight basis.

http://en.wikipedia.org/wiki/File:Soxhlet_mechanism.gif



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33

Experiment- 8- Total Carbohydrates

Objective To find out the amount of total carbohydrates in a given food sample. Theory Carbohydrates are the important components of storage and structural materials in the plants. They exist as free sugars and polysaccharides. The basic units of carbohydrates are the monosaccharides which cannot be split by hydrolysis into more simpler sugars. The carbohydrate content can be measured by hydrolyzing the polysaccharides into simples sugars by acid hydrolysis and estimating the resultant monosaccharides. Principle Carbohydrates are first hydrolysed into simple sugars using dilute hydrochloric acid. In hot acidic medium glucose is dehydrated to hydroxymethyl furfural. This compound forms with anthrone a gree colored product with an absorption maximum at 630nm. Materials

2.5 N-HCl

Anthrone Reagent: Dissolve 200mg anthrone in 100mL of ice cold 95% H2SO4. Prepare fresh before use.

Standard Glucose: Stock – Dissolve 100mg in 100mL water. Working standard – 10mL of stock diluted to 100mL with distilled water. Store refrigerated after adding a few drops of toluene.

Procedure 1. Weigh 100mg of the sample into a boiling tube. 2. Hydrolyse by keeping it in boiling water bath for 3 hours with 5mL of 2.5 N-HCl and cool to room

temperature. 3. Neutralise it with solid sodium carbonate until the effervescence ceases. 4. Make up the volume to 100mL and centrifuge. 5. Collect the supernatant and take 0.5 and 1mL aliquots for analysis. 6. Prepare the standards by taking 0, 0.2, 0.4, 0.6, 0.8 and 1mL of the working standard. ‘0’ serves as blank. 7. Make up the volume to 1mL in all the tubes including the sample tubes by adding distilled water. 8. Then add 4mL of anthrone reagent. 9. Heat for eight minutes in a boiling water bath. 10. Cool rapidly and read the green to dark green color at 630nm. 11. Draw a standard graph by plotting concentration of the standard on the X-axis versus absorbance on the

Y-axis. 12. From the graph calculate the amount of carbohydrate present in the sample tube. Calculation

Note Cool the contents of all the tubes on ice before adding ice-cold anthrone reagent.

Amount of carbohydrate present in 100mg of the sample = mg of glucose

X 100 Volume of test sample



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35

Experiment- 9- Crude Fiber

Objective To find out the amount of crude fiber in a given food sample.

Theory Crude fiber consists largely of cellulose and lignin (97%) plus some mineral matter. It represents only 60% to 80% of the cellulose and 4% to 6% of the lignin. The crude fiber content is commonly used as a measure of the nutritive value of poultry and livestock feeds and also in the analysis of various foods and food products to detect adulteration, quality and quantity. Principle During the acid and subsequent alkali treatment, oxidative hydrolytic degradation of the native cellulose and considerable degradation of lignin occur. The residue obtained after final filteration is weighed, incinerated, cooled and weighed again. The loss in weight gives the crude fiber content. Materials 1. Sulphuric acid solution (0.255 ±0.005N) : 1.25g concentrated sulphuric acid diluted to 100mL

(concentration must be checked by titration) 2. Sodium hydroxide solution (0.313 ±0.005N) : 1.25g sodium hydroxide in 100mL distilled water

(concentration must be checed by titration with standard acid) Procedure 1. Extract 2g of ground material with ether or petroleum ether to remove fat (Initial boiling temperature 35

-38°C and final temperature 52°C). if fat content is below 1%, extraction may be omitted. 2. After extraction with ether boil 2g of dried material with 200mL of sulphuric acid for 30min with

bumping chips. 3. Filter through muslin and wash with boiling water until washing are no longer acidic. 4. Boil with 200mL of sodium hydroxide solution for 30min. 5. Filter through muslin cloth again and wash with 25mL of boiling 1.25% H2SO4, three 50mL portions of

water and 25mL alcohol. 6. Remove the residue and transfer to ashing dish (preweighed dish W1). 7. Dry the residue for 2h at 130 ±2°C. Cool the dish in a desiccator and weigh (W2). 8. Ignite for 30min at 600 ±15°C. 9. Cool in a desiccator and reweigh (W3). Calculation

% crude fiber in ground sample = Loss in weight on ignition (W2 - W1) – (W3 - W1)

x 100 Weight of the sample



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37

Experiment- 10- Determination of pH using pH paper and Universal Indicator

Objective To determine the pH of a given sample using pH paper and Universal Indicator. Theory There are millions of chemical substances in the world, some are acids, others are bases and some are neutral. Acids and Bases Acids are substances that produce free hydrogen ions (H+ ions) when dissolved in water. Bases are substances that produce hydroxyl ions (OH- ions) when dissolved in water. Acidic solutions are rich in hydrogen ions and basic solutions are poor in hydrogen ions. Some acids dissociate only partly, releasing very small amounts of H+ ions, and are called weak acids. Others dissociate completely, releasing large amounts of H+ ions, and are called strong acids. In the same way, bases that dissociate partly are called weak bases and those that dissociate completely are called strong bases. pH of a Solution The acidic or basic property of substances is measured in terms of pH. It is a measurement of the hydrogen ion concentration. pH is defined as the negative logarithm (base 10) of hydrogen ion concentration.

If the hydrogen ion concentration is very high, the pH value is very low. This is determined using a scale ranging from 0-14 called the pH scale. It was introduced by a Danish chemist Soren Peder Lauritz Sorensen. Substances with pH lower than 7 are acidic, those with pH equal to 7 are neutral and those with pH greater than 7 are basic in nature. The pH of pure water is 7. i.e.,

Figure 9 Danish Chemist Soren Peder Lauritz Sorensen



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Figure 10 pH Scale

pOH of a Solution pOH is used to measure the concentration of hydroxyl ions (OH- ions) or the alkalinity of a solution. pOH is defined as the negative logarithm (base 10) of hydroxyl ion concentration.

pOH is derived from pH and are related by the equation,

Measurement of pH pH of a solution is measured using pH indicators. pH indicators are substances that changes colour when in contact with acidic, basic or neutral solutions. Let us discuss some pH measurement methods. pH paper pH paper is a strip of special paper that is prepared by dipping the strip in different chemical compounds and then drying it. It can be used to find the approximate pH of any solution. These paper changes colour when immersed in acidic or basic solutions. To determine the pH, the pH paper is dipped in a given sample solution and the colour developed in the paper is compared with the colour chart and the approximate pH of the solution can be identified. It is commerically available as test papers.

Figure 11 pH Paper

Universal Indicator Universal indicator is a pH indicator composed of different chemical compounds. When the indicator is poured in the sample solution, the mixture obtained exhibits a smooth colour change over a pH value



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ranging from 1-14 that indicates the acidic or basic property of the solution. It is commercially available as test solutions.

Figure 12 Universal pH Indicator

pH Meter pH meter is an electronic instrument consisting of a special bulb that is sensitive to hydrogen ions that are present in the test solution. The signal produced by the bulb is amplified and sent to an electronic meter connected to the bulb, which measures and display the pH reading. It gives more precise values than the pH papers. For very precise measurement, the pH meter should be calibrated before each measurement. The calibration should be performed with at least two buffer solutions with known pH. For general purposes, buffer solutions with pH 4 and pH 10 are used. For more precise measurements, three buffer solution calibrations are preferred. After each single measurement, the bulb is rinsed with distilled water or deionised water to remove any traces of solution being measured. Then the bulb is blotted with a blotting paper to remove remaining water that could dilute the sample and alter the reading. When not in use, the bulb must be kept wet at all times to avoid dehydration of the pH sensing membrane.

Figure 13 A Digital pH Meter

Red Cabbage Juice This is a blue-violet coloured liquid. When it comes in contact with acidic substances, it becomes red. When it comes in contact with basic substances, it becomes green or even yellow.



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Figure 14 Colour Scale of Red Cabbage Papers

pH helps to determine the acidic and basic strength of acids and bases.

Figure 15 Materials Required

Procedure

Real Lab Procedure Determination of pH using pH Paper

Take a pH paper strip and place it on a white tile.

Pour a drop of the sample on the pH paper using a clean dropper.

Observe the colour of the pH paper.

Now compare the colour obtained on the pH paper with the different colour shades of the standard colour pH chart and note down the pH value.

Similarly, find the pH of the remaining samples using a fresh strip of pH paper and a separate dropper for each sample.

Determination of pH using Universal Indicator Solution

Take a small quantity of the given sample in a test tube using a dropper.



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Using a dropper pour a few drops of the universal indicator solution into the test tube containing the sample.

Shake the test tube well and note the colour developed in the test tube.

Now compare the colour produced in the test tube with the different colour shades of the standard colour pH chart and note down the pH value.

Similarly, find the pH of the remaining samples. Simulator Procedure (as performed through the Online Labs)

Simulator Link- http://amrita.olabs.edu.in/?sub=73&brch=7&sim=144&cnt=4

You can select the aqueous solution from the 'Select the aqueous solution' drop down list.

Now choose any one of the sample solutions in the beaker by clicking on it.

You can find out the pH value of the solution using any of the two methods mentioned below. Using pH Paper

Drag the dropper towards the beaker and dip it into the solution to take the solution in it.

Still holding the dropper, move it from the beaker over to the pH paper and release it to pour a few drops of the solution on to the pH paper .

The area on the pH paper over which the solution is poured develops a colour.

To find the pH value of the solution, select the colour strip from the standard colour pH chart and drag it to the pH paper to compare it.

The colour that matches with the spot on the pH paper indicates the pH value of the solution. Using Universal Indicator Solution

Click on the dropper in the universal indicator solution bottle and drag it towards the solution in the beaker to pour the universal indicator into it.

The solution changes colour.

To find the pH value of the solution, select the colour strip from the standard colour pH chart and drag it near to the solution in the beaker to compare it.

The colour that matches with the colour of the solution in the beaker indicates the pH value of the solution.

Observations Record the observations in a tabular column.

Sample Name For pH Paper For Universal Indicator Solution

Colour produced on the pH Paper

Approximate pH Colour produced in the solution

Approximate pH

Precautions

Use only the standard colour pH chart supplied with the pH paper for assessing the pH value.

Keep the pH strips away from chemical fumes.

Either use fresh fine dropper or glass rod for each different sample, or wash the dropper or glass rod well with water every time.

http://amrita.olabs.edu.in/?sub=73&brch=7&sim=144&cnt=4



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To correctly view the colour produced on the pH paper, keep the pH paper on a white tile while performing the experiment.

Video Link- https://www.youtube.com/watch?v=-lbh5_1xxtI

https://www.youtube.com/watch?v=-lbh5_1xxtI



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44

Experiment- 11- Determination of pH using pH Meter

Objective To determine the pH of a given sample using ph Meter. Theory Chemists, biologists, environmentalists and lab technicians alike all use pH to measure the acidic and basic potentials of a solution. A pH meter is very useful and the most accurate tool available to test pH levels. It measures the potential usable amount of free moving hydrogen atoms versus the amount of available negatively charged protons. More hydrogen = acidic = pH number less than 7. More protons = basic = pH number greater than 7. Understanding pH

Figure 16 Learn about how acids and bases are defined

Acidity and alkalinity (the term used to describe bases) are both defined by the hydrogen ions they lose or accept. An acid is a substance that loses (or, some say, donates) hydrogen ions. A base is a substance that accepts additional hydrogen ions.

Figure 17 Understand the pH scale

The pH number is used to rate the level of acidity or alkalinity of water soluble substances. Water normally contains an equal amount of hydroxide ions (OH-) and hydronium ions (H30+). When an acidic or alkaline substance is added to water, they change the proportion of hydroxide and hydronium ions.



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It is typically said to be on a scale of 0 to 14 (though substances can actually be fall beyond that range). Neutral substances rate close to 7, acidic ones below 7, and alkaline substances are above 7. The pH scale is a logarithmic scale, meaning that differences of a single integer actually represent a tenfold difference in acidity or alkalinity. For instance, a substance that has a pH of 2 is actually ten times more acidic than one with a pH of 3 and 100 times more acidic than a substance with a pH of 4. The scale functions similarly for alkaline substances, with one integer representing a tenfold difference in alkalinity.

Figure 18 Get to know why we test the pH of water

Pure water should have a pH of 7, though common tap water has a pH between 6 and 5.5. Highly acidic water (water with a low pH) is more likely to dissolve toxic chemicals. These can contaminate the water and make it unsafe for human consumption. It is often considered best to test pH on site. If you collect a water sample for study in a lab, carbon dioxide in the air can dissolve into the water. The dissolved carbon dioxide reacts with the ions in the water to increase acidity in basic or neutral solutions. To prevent carbon dioxide contamination, you must test water within 2 hours of collection. Procedure Using Benchtop Model pH Meter in Laboratory Source- http://www.wikihow.com/Calibrate-and-Use-a-pH-Meter

Figure 19 Step-1 Turn on pH meter

http://www.wikihow.com/Calibrate-and-Use-a-pH-Meter



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Figure 20 Step-2 Eait around 30 minutes for the electronics to warm up

Figure 21 Step-3 Take electrode out of storage solution

Figure 22 Step- 4 Rinse the electrode with distilled water



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Figure 23 Step-5 Submerse the electrode into the pH 7 buffer

Figure 24 Step- 6 Press the calibrate button

Figure 25 Step-7 Recalibrate



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Figure 26 Step- 8 Rinse the electrode

Figure 27 Step- 9 Submerse the electrode into the pH 4 buffer

Figure 28 Step- 10 Wait until the pH icon stops flashing and press the measure button



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Figure 29 Step- 11 Rinse the electrode

Figure 30 Step- 12 Submerse the electrode in the sample

Figure 31 Step- 13 Press the measure button



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Figure 32 Step- 14 Record the pH of the sample

Using pocket pH meter in the field Source- http://www.wikihow.com/Measure-the-pH-of-Water

Figure 33 Calibrate the probe and meter following the manufacturer specifications

You may need to calibrate the meter by testing it in a substance with a known pH rating. You can then adjust the meter accordingly. If you will be testing water away from a lab, you may want to perform this calibration several hours before you take the meter to the field. Rinse the probe with clean water before using it. Dry it off with a clean tissue.

Figure 34 Collect a sample of the water in a clean container

http://www.wikihow.com/Measure-the-pH-of-Water



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The water sample must be deep enough to cover the tip of the electrode. Let the sample sit for a moment so the temperature can stabilize. Measure the temperature of the sample using a thermometer.

Figure 35 Adjust the meter to match the sample temperature

The probe's sensitivity is affected by the temperature of the water, and so the reading of the meter cannot be accurate if you do not input the temperature data.

Figure 36 Put the probe into the sample

Wait for the meter to come to equilibrium. The meter has reached equilibrium when the measurement becomes steady.

Figure 37 Read the pH measurement of the sample

Your pH meter should provide a reading on the scale of 0-14. If the water is pure it should read close to 7. Record your findings. Observations and Calculations



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Sample No. Sample Name Temperature of sample (°C) pH



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54

Experiment- 12- Determination of acidity of given honey sample

Theory

Food acids are usually organic acids, with citric, malic, lactic, tartaric, and acetic acids being the most

common. However, inorganic acids such as phosphoric and carbonic acids (arising from carbon dioxide in

solution) often play an important and even predominant role in food acidulation.

The organic acids present in foods influence:

Flavor (i.e., tartness)

Color (through their impact on anthocyanin and other pH-influenced pigments)

Prevent/retard the growth of microorganisms or inhibit the germination of spores

Providing the proper environment for metal ion chelation, an important phenomenon in the

minimization of lipid oxidation

Organic acids may present:

Naturally,

By Fermentation

Added as part of a specific food formulation

The importance of determining food acidity

1. Determine the degree of maturity of fruits and vegetables- The titratable acidity of fruits is used, along

with sugar content, as an indicator of maturity, generally the higher the maturity, the lower the acid

content e.g. in the ripening process, such as tomatoes from green to mature stage , there is an increase

in sugar content.

2. To determine the freshness of foods- For example in milk, the more the lactic acid levels, means that

milk is rotten.

3. Acidity indicators reflect the quality of food- The amount of organic acids in food directly affects the

food flavor, color, stability, and the level of quality.

4. Determination of acid on the microbial fermentation process- Such as fermentation products in soy

sauce, vinegar and other acids is an important indicator of quality.

There are two ways to express food acidity:

1. Titratable acidity

• Simple estimate of the total acid content of food

• Better predictor of acid impact on flavour

2. Hydrogen concentration pH

• Depend on the strength of acid condition

Objective



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To determine the acidity of a given Honey sample.

Reagents

Standard Sodium Hydroxide solution – 0.05 N

Phenolpthalein indicator – Dissolve 0.5 gm Phenolpthalein in 100 ml of 50% ethyl alcohol (v/v)

Procedure

1. Take 10 gm of the sample in a suitable titration flask and dissolve in 75 ml of carbon dioxide free

water.

2. Mix thoroughly.

3. Titrate against standard sodium hydroxide solution using 4-6 drops of phenolphthalein indicator till

pink colour persists for 10 seconds.

4. Determine blank on water and indicator and correct the volume of sodium hydroxide solution used.

Calculation

Acidity as formic acid (%) by weight =

Where,

V = corrected volume of 0.05 N Sodium Hydroxide used

M = weight in gm of the sample taken for test

(Ref: - I.S.I. Handbook of Food Analysis (Part II) 1984 page 37)



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57

Experiment- 13- Determination of acidity of extracted fat in a given sample of biscuit

Objective

To determine the acidity of extracted fat in a given sample of biscuit.

Apparatus

Soxhlet Apparatus – with a 250 mL flat bottom flask.

Reagents

Petroleum Ether – Boiling point 40 to 80°C

Benzene- Alcohol–Phenophthalein Stock solution – To one L of distilled benzene add one L of alcohol

or rectified sprit and 0.4 gm of phenophthalein. Mix the contents well.

Standard sodium hydroxide solution – 0.05N

Procedure

1. Weigh accurately sufficient amount. of biscuit powder (20 – 25 gm) which will yield 3- 4 gm of fat

and transfer it to a thimble and plug it from the top with extracted cotton and filter paper.

2. In case of filled and coated biscuits the weight of the biscuits includes the filling and coating

material.

3. Dry the thimble with the contents for 15 to 30 minutes at 100°C in an oven. Take the weight of

empty dry soxhlet flask.

4. Extract the fat in the soxhlet apparatus for 3 to 4 hours and evaporate off the solvent in the flask on

a water bath.

5. Remove traces of the residual solvent by keeping the flask in a hot air oven for about 30 minutes.

Cool the flask.

6. Weigh accurately about 3.0 gm of extracted fat in a 250 mL conical flask and add 50 mL of mixed

benzene-alcohol-phenolphthalein reagent and titrate the contents to a distinct pink color with the

Sodium hydroxide solution taken in a 10 mL micro burette.

7. If the contents of the flask appear cloudy during titration add another 50 mL of the reagent titration.

Make a blank titration with 50 mL of the reagent.

8. Subtract from the titer of the fat, the blank titer.

Calculation

Acidity of extracted fat (as oleic acid) % by weight =

Where, V = Volume of 0.05N Sodium hydroxide solution used in titration after subtracting the blank N= Normality of Sodium hydroxide (determined using Potassium phthalate) W1 = weight in gm of soxhlet flask containing fat W = weight in gm of the empty soxhlet flask (Ref: - IS 1011: 1992 Biscuits – Specification)



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59

Experiment- 14- Determination of reducing and non- reducing sugars in a given food sample

Objective

To determine the reducing and non- reducing sugars in a given food sample.

Reagents

Fehling A: Dissolve 69.28-g copper sulphate (CuSO4.5H2O) in distilled water. Dilute to 1000 ml. Filter

and store in amber coloured bottle.

Fehling B: Dissolve 346 g Rochelle salt (potassium sodium tartrate) (K Na C4H4O6. 4H2O) and 100 g

NaOH in distilled water. Dilute to 1000 ml. Filter and store in amber coloured bottle.

Carrez 1 – Add 21.9 g Zinc acetate and 3 ml acetic acid in a 100 ml volumetric flask. Make up the

volume with water.

Carrez 2 – 10.6 % aqueous solution of Potassium ferrocyanide.

Methylene Blue Indicator: Prepare 1% of methylene blue solution in distilled water.

Procedure

1. Weigh accurately about 5 g sample, transfer to a 200 ml volumetric flask dissolve in warm water,

dilute to about 150 ml.

2. In case solution is not clear, add 5 ml of Carrez 1 solution followed by 5 ml of Carrez 2 solution.

3. Make up to 200 ml.

4. Filter through a dry filter paper.

5. Titrate the solution obtained as such to determine % Reducing sugars.

Preliminary Titration:

1. Pipet 5 ml each of Fehling A and B into 250 ml conical flask.

2. Mix and add about 10 ml water and a few boiling chips or glass beads.

3. Dispense solution.

4. Heat the flask to boiling.

5. Add 3 drops of methylene blue indicator.

6. Continue the addition of solution dropwise until the blue colour disappears to a brick-red end

point. The concentration of the sample solution should be such that the titre value is between

15 and 50 ml.

7. Note down the titre value.

Final Titration:

1. Pipet 5 ml each of Fehling A and B. Add sample solution about 2 ml less than titre value of the

preliminary titration.

2. Heat the flask to boiling with in 3 minutes and complete the titration.

3. Perform the titration duplicate and take the average.

4. Calculate the reducing sugar % as shown below.



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Reducing Sugars % =

Determination of Sucrose

1. Take an aliquot of the filterate obtained in Reducing sugar method and invert it with Hydrochloric acid in a water bath at 60º C by keeping for 10 minutes.

2. Cool immediately and neutralize with sodium hydroxide and finally with sodium carbonate. 3. Make upto volume and determine reducing sugar by Lane and Eynon method.

Non- Reducing Sugars % (As Invert Sugar)=

Determination of Factor (for Invert Sugar) of Fehling Solution:

1. Accurately weigh around 4.75 g of analar grade sucrose.

2. Transfer to 500 ml volume flask with 50 ml distilled water.

3. Add 5 ml conc. HCl and allow to stand for 24 hours Neutralize with NaOH solution and make up to

volume.

4. Mix well and transfer 50 ml to a 100 ml volumetric flask and makeup to volume.

5. Transfer to a burette having an offset tip.

6. Perform the titration of Fehling solution following the similar procedure as above:

Fehling Factor (As Invert Sugar)=

[Ref: - IS: 6287-1985 (Reaffirmed 2010) Methods of Sampling and Analysis for Sugar Confectionery]



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Experiment- 15- Determination of Vitamin- C (Ascorbic Acid) in a given food sample

Objective

To determine the Vitamin- C (Ascorbic Acid) in a given food sample.

Theory

The ascorbic acid content in fruits and vegetables can be estimated by macerating the sample with

stabilising agents such as 20% metaphosphoric acid.

Principle

2, 6 -dichlorophenol indophenol is reduced to a colourless form by ascorbic acid. The reaction is specific for

ascorbic acid at pH 1 to 3.5. The dye is blue in alkaline solution and pink in acid.

Reagents

1. Standard Indophenol Solution

1.1. Dissolve 0.05 gm 2, 6 dichlorophenol indophenol in 50 mL water, to which 42 mg sodium carbonate

is added, and make upto 200 mL. with water and filter.

1.2. Sodium carbonate is added for stability purpose.

1.3. The dye solution keeps for a few weeks if stored in refrigerator. Prepare fresh if possible and

standardize before use.

Blank correction:

1.4. Dissolve 50 mg 2, 6-dichloroindophenol Na salt that has been stored in desiccator over soda lime, in

50 mL H2O to which has been added 42 mg NaHCO3; shake vigorously, and when dye dissolves,

dilute to 200 mL with H2O.

1.5. Filter through fluted paper into amber glass-stoppered bottle.

1.6. Keep stoppered, out of direct sunlight, and store in refrigerator.

1.7. Decomposition products that make end point in distinct occur in some batches of dry indophenol

and also develop with time in stock solution.

1.8. Add 5.0 mL extracting solution containing excess ascorbic acid to 15 mL dye reagent.

1.9. If reduced solution is not practically colorless, discard, and prepare new stock solution.

1.10. If dry dye is at fault, obtain new supply.)

1.11. Transfer three 2.0 mL aliquots ascorbic acid standard solution to each of three 50 mL

Erlenmeyers containing 5.0 mL HPO3–CH3COOH solution, B(a)(1).

1.12. Titrate rapidly with indophenol solution from 50 mL burette until light but distinct rose pink

persists 5 s.

1.13. Each titration should require ca 15 mL indophenol solution, and titrations should check

within 0.1 mL).

1.14. Similarly titrate 3 blanks composed of 7.0 mL HPO3–CH3COOH solution, B(a)(1), plus volume

H2O ca equal to volume indophenol solution used in direct titrations.

1.15. After substracting average blanks (usually ca 0.1 mL) from standardization titrations,

calculate and express concentration of indophenol solution as mg ascorbic acid equivalent to 1.0 mL

reagent.



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1.16. Standardize indophenol solution daily with freshly prepared ascorbic acid standard solution.

2. Standard Ascorbic acid solution – Dissolve 0.05 gm pure ascorbic acid in 60 mL of 20% metaphosphoric

acid (HPO3) and dilute with water to exactly 250 mL in a volumetric flask.

3. Metaphosphoric acid - 20 %

4. Acetone

Standardisation of Dye

1. Pipette 10 mL of standard Ascorbic acid solution in a small flask and titrate with indophenol solution

until a faint pink colour persists for 15 seconds.

2. Express the concentration as mg Ascorbic acid equivalent to 1 mL of dye solution i.e. 10 mL of Ascorbic

acid solution = 0.002 gm ascorbic acid.

3. If 0.002 gm ascorbic acid requires V mL dye solution to neutralize it then 1 mL dye solution = 0.002/V gm

ascorbic acid.

Procedure

1. Pipette 50 mL of unconcentrated juice (or the equivalent of concentrated juice) into a 100 mL volumetric

flask, add 25 mL of 20% metaphosphoric acid as stabilizing agent and dilute to volume.

2. Pipette 10 mL in a small flask and add 2.5 mL acetone.

3. Titrate with indophenol solution until a faint pink colour persists for 15 seconds.

Calculation

Vitamin C (mg/100mL juice) = 20 *(V) *(C)

Where,

V = mL indophenols solution,

C = Vitamin C per mL indophenol solution

Note

Acetone may be omitted if sulphur dioxide is known to be absent. Its function is to form the acetone

bisulphate complex with sulphur dioxide which otherwise interferes with the titration. Sometime a small

proportion of the ascorbic acid in foods becomes reversibly oxidized during aging and forms dehydroascorbic

acid. If this is suspected, first estimate the ascorbic acid as above, then through another portion of the

solution pass a stream of Hydrogen sulphide for 10 minutes. Stopper the flask and allow it to stand overnight

in a refrigerator. Then remove hydrogen sulphide by bubbling nitrogen through the mixture and titrated as

before. The difference between the two titrations gives a measure of the dehydroascorbic acid. One

international unit of vitamin C = 50 μg ascorbic acid.

(Ref :- FAO Manuals of Food Quality Control 14 / 8, page 194 / Pearson’s Composition and Analysis of Foods

9th edn,1991, page 264 and AOAC Official Method 967.21 Ascorbic acid in Vitamin preparation and juices )



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Experiment- 16- Determination of Diastase enzyme (α- amylase) activity in a given food sample by Falling Number test

Objective

To determine the Diastase enzyme (α- amylase) activity in a given food sample by Falling Number test.

Theory

The Falling Number test provides an index of -amylase in a ground wheat or flour sample. The procedure

relies on the reduction in viscosity of starch paste caused by the action of -amylase. The method is based

on the unique ability of alpha-amylase to liquefy a starch suspension. Gelatinization strength is measured by

falling number as “time in seconds” required stirring and allowing the stirrer to fall a measured distance

through hot aqueous flour gel undergoing liquefaction. The starch gelatinizes, and the -amylase liquefies

the resultant paste. The time it takes (in seconds) for the viscometer stirring rod to fall through the starch

paste is the Falling Number. Wheat sample made from sprout-damaged wheat can have a Falling Number of

100s or less. Bread wheat with average -amylase activity has a falling Number of approximately 250s. The

upper limit for the Falling Number test is approximately 400s, which occurs for wheat devoid of -amylase.

Requirements

Analytical balance

Wheat grains

Grinder

Falling Number apparatus

Procedure

1. Ensure that the water level in the gauge is up to the mark.

2. Ensure that water connection for cooling of the instrument.

3. Switch on the mains.

4. The distilled water in bath is brought to boil.

5. Weigh 7 g of g ground wheat, transfer it to viscometric tube, and add 25 ml of distilled water, rubber

the tube and shake vigorously for obtaining a uniform suspension.

6. Remove stopper and push down flour adhering to sides with the viscometer stirrer.

7. Place the tube with stirrer in the boiling water bath. Start the timer and the instrument.

8. After 5 seconds, automatic stirring starts at the rate of 2 stirs/seconds for 60 seconds.

9. After a total of 60 seconds stirring automatically stops releasing the stirrer at its uppermost position

and allows falling by its weight at a fixed distance and time is recorded in seconds

Precautions

Ensure that the discharge hose is placed in the sink.

The water tap should be on for cooling the apparatus.

Handle the viscometer tube gently.

Observations



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Wheat Grains

Falling Number (s) Mean

Standard Deviation Variety 1

Variety 2 Variety 3

Hard wheat

Soft wheat

Interpretation of results

Falling number (in seconds) Interpretation

Below 150 Sprouted wheat, high alpha-amylase activity.

200-250 Normal alpha-amylase activity.

300 and above Amylase activity too low.



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Experiment- 17- Identification of pigments in a given food sample by paper chromatography

Objective

To identify different pigments present in a given food sample by paper chromatography.

Theory

The word chromatography originated from two greek words 'chroma' meaning 'colour' and 'graphine'

meaning 'to write'. Chromatography means colour writing and it was first employed by a Russian scientist

Mikhail Tsvet. This method was first used for the separation of coloured substances in plants.

In the chromatographic technique, the mixture of substances is applied onto a phase called the stationary

phase. The stationary phase may be solid or liquid. A moving phase that can be a pure solvent or a mixture

of solvents, or a gas is allowed to move slowly over the stationary phase. This moving phase is called the

mobile phase. When the mobile phase is moved over the mixture on the stationary phase, the components

of the mixture gradually separates from one another.

Paper Chromatography

In paper chromatography, the stationary phase is a special quality paper called chromatography paper.

Mobile phase is a solvent or a mixture of solvents. A solution of the mixture is spotted on a line about 2 cm

above from the bottom of the paper, called original line or base line and then suspended in a

chromatography chamber containing suitable solvent. The solvent rises up the paper by capillary action and

flows over the spot. The paper selectively retains different components according to their differing partition

in the two phases. The paper strip so developed is called Chromatogram. The spots of the separated

coloured compounds are visible at different heights from the position of initial spot on the chromatogram.

The spots of the separated colourless components may be observed either under ultraviolet light or by the

use of an appropriate spray reagent. The distance travelled by the solvent from the original line is called

solvent front. The relative adsorption of each component of the mixture is expressed in terms of its

Retardation factor (Rf) (Retention factor).

Figure 38 Paper Chromatography



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Requirements

Figure 39 Requirement for Paper Chromatography experiment

Procedure

1. Take a Whatman filter paper strip and using a pencil draw a horizontal line 4cm from one end of the paper. Then draw another line lengthwise (verticallly) from the centre of the paper. Name the point at which the two lines intersect as P.

2. Using a fine capillary tube, put a drop of the extract of spinach leaves at the point P. Let it dry in air. 3. Put another drop on the same spot and dry again, so that the spot is rich in the leaf extract. 4. Pour equal amounts of isopropyl alcohol and distilled water into a chromatographic chamber and

mix it well using a glass rod. This is used as the solvent. 5. Suspend the filter paper vertically in the chromatographic chamber containing the solvent in such a

way that the pencil line remains about 2cm above the solvent level. 6. Close the jar with its lid and keep it undisturbed. 7. Notice the rising solvent along with the coloured components of the leaf extract. 8. After the solvent has risen to about 15 cm you will notice two different spots of coloured

components on the filter paper. 9. Take the filter paper out of the jar and using a pencil mark the distance that the solvent has risen on

the paper. This is called the solvent front. 10. Dry the filter paper and put pencil marks at the centre of each spot. 11. Measure the distance of each spot from the original line and the distance of the solvent front from

the original line. 12. Calculate the Rf values of different components of leaf extract by using the formula,

Precautions Use good quality pencil for drawing the reference line so that the mark does not dissolve in the

solvent in which the chromatography is carried out.

Always use a fine capillary tube.



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Keep the jar undisturbed and covered during the experiment.

The spot should be small and rich in mixture.

Allow the spot to dry before putting the strip in the jar.

Keep the strip erect. Do not let it curl.

Do not allow the spot to dip in the solvent. Observations

Sl. No

Component Distance travelled by the component from the original line (cm)

Distance travelled by the solvent from the original line (cm)

Rf value

1. Orange (Carotene)

2. Yellow (Xanthophyll)

3. Light green (Chlorophyll a)

4. Dark green (Chlorophyll b)

Inference

Rf value of orange (Carotene) = ……………

Rf value of Yellow (Xanthophyll) = …………..

Rf value of Light green (Chlorophyll a) = …………..

Rf value of Dark green (Chlorophyll b) = …………..



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72

Experiment- 18- Effect of Baking Soda in CO2 production

Objective

To observe the effect of baking soda in CO2 production.

Theory

Baking soda (NaHCO3) Sodium bicarbonate has the property of releasing CO2 when it is heated:

2NaHCO3 → Na2CO3 + H2O + CO2

Vinegar (HC2H3O2) is a solution of acetic acid. It reacts with baking soda, sodium bicarbonate (NaHCO3), to

produce carbon dioxide gas (CO2) and an aqueous solution of sodium acetate (NaC2H3O2). The reaction can

be written as follows:

NaHCO3 (aq) + HC2H3O2 (aq) ------> CO2 (g) + H2O (l) + NaC2H3O2 (aq)

Requirements

Safety Goggles

Balloon

Bottle with a narrow neck

Funnel or straw

Water

Vinegar

Baking soda

Procedure

Pour about an inch of liquid (half vinegar, half water) into the bottle.

Use the funnel to fill the balloon half full of baking soda.

Stretch the open end of the balloon over the neck of the bottle. Make sure it's on tight. Let the

heavy end of the balloon dangle, so no baking soda goes in the bottle.

Hold onto the balloon at the bottle neck, and pick up the heavy part of the balloon so that all the

baking soda falls into the vinegar at the bottom of the bottle.

If the balloon does not begin to expand right away, shake the soda bottle slightly to mix the baking

soda and vinegar.



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74

Experiment- 19- Detection of Saccharine in beverages

Objective

To test the presence of Saccharine in the given sample of beverage.

Procedure

1. Curdle an aliquot of the diluted sample (about 25 ml) with dilute acetic acid. 2. Shake well and filter. 3. Acidify the clear filtrate with 2.0 ml of concentrated hydrochloric acid, and extract with two 25 ml

portions of diethyl ether. 4. Draw off the aqueous layers and wash the combined ether extract with three successive portions of 5 ml

of water, evaporate the ether extract on a water bath, add a drop or two of water, mix well with glass rod and taste a little.

5. A characteristic sweet taste indicates the presence of saccharin. 6. Confirm by heating with NaOH and detecting Salicylic acid from thereby.

Conversion to salicylic acid 1. Acidify about 20 -25 ml of filterate obtained above and extract with three portions of ether as above. 2. Wash ether extract with two 5 ml portions of water, evaporate greater portion of ether in porcelain dish

on steam bath, let remainder evaporate spontaneously and add 1 drop of 0.5% (v/v) neutral FeCl3 solution.

3. Violet colour indicates Salicylic acid. (Ref: A.O.A.C. 17th edn,2000 Official Method 941.10 Saccharin in Food read with A.O.A.C. Official Method 975.30 Salicylic acid in Food and Beverages)



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76

Experiment- 20- Visit to hospital/slide show on various nutritional deficiency disorders

Objective

To know about various nutritional deficiency disorders.

Presentation



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78




79

INDEX Ash - Total ............................................................................ 10

Ash- Acid Insoluble .............................................................. 14

Crude Fat- Soxhlet Apparatus Method ................................. 29

Crude Fiber ........................................................................... 35

Crude Protein- Kjeldahl Method ........................................... 17

Crude Protein- Protein by Kjeltec ......................................... 24

Detection of Saccharine in beverages ................................... 74

Determination of acidity of extracted fat in a given sample of

biscuit .............................................................................. 57

Determination of acidity of given honey sample .................. 54

Determination of Diastase enzyme (α- amylase) activity in a

given food sample by Falling Number test ...................... 65

Determination of pH using pH Meter ................................... 44

Determination of pH using pH paper and Universal Indicator

......................................................................................... 37

Determination of reducing and non- reducing sugars in a

given food sample ............................................................ 59

Determination of Vitamin- C (Ascorbic Acid) in a given food

sample .............................................................................. 62

Effect of Baking Soda in CO2 production ............................. 72

Identification of pigments in a given food sample by paper

chromatography ............................................................... 68

Moisture Content- Lab Oven Method ..................................... 4

Moisture Content- Using Moisture Meter ............................... 7

Temperature ......................................................................... 25

Total Carbohydrates .............................................................. 33

Visit to hospital/slide show on various nutritional deficiency

disorders .......................................................................... 76

food chemistry and nutrition practical manual · 03/08/2015 · food chemistry and nutrition-...

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