Applied Chemistry Manual DYPSEM Final
Applied Chemistry Manual DYPSEM Final
……………… Division Batch ………… having Roll No. …………… has satisfactorily
Date:
CERTIFICATE
This is to certify that Mr./Miss …………………………………………… ………………………………….
of …………. ………..Year student of ………………………….. Department from ………….. ………...
……………… Division Batch ………… having Roll No. …………… has satisfactorily
completed all the experiments in the course …………….. during the academic year
……………….. in the laboratories of D.Y. Patil College of Engineering & Tech., Kolhapur.
Date: ………….
Faculty H.O.D.
Department of First Year Engineering
CONTINUOUS ASSESSMENT SHEET
Course Objective:
1 To test water quality parameters using various titration analysis methods
2 To synthesize simple advanced materials and estimate concentration of
elements in material’s.
3 To know handling of glassware’s and simple equipment’s for chemical
Analysis
LIST OF EXPERIMENTS
Exp. Duration
Title of Experiment
No.
Determination of total hardness and of water sample by EDTA
1 02 Hrs.
method. (Complexometric Titration).
Experiment No. 1
Title: Hardness of Water
Date:
EXPERIMENT No. 1
HARDNESS OF WATER
AIM: To determine the hardness of given samples of water by standard EDTA
method.
THEORY:
Various salts present in water cause hardness to water. These salts are
carbonates, bicarbonates, chlorides, sulphates of calcium & magnesium. When
water is allowed to react with soaps, the hardness causing salts react first with
soaps to form a substance called as scum. Scum has no commercial value. It is
light in weight & therefore always floats on water. After all the salts react with
water to form scum, soap reacts with water to give foam. Due to this behavior,
hardness causing salts are called as soap consuming substances. The hardness is
of two types.
i) Temporary or carbonate hardness & ii) Permanent or non-carbonate hardness.
Temporary hardness is due to presence of carbonates & bicarbonates of Ca &
Mg. It can be removed by boiling the water sample. Permanent hardness is due
to sulphates, chlorides & nitrates of Ca & Mg. It cannot be removed by boiling.
Total hardness is combination of temporary & permanent hardness. Total
hardness can be found out by calculating equivalent amounts of hardness
producing substances in terms of calcium carbonate. It is expressed as in parts
per million (ppm) of calcium carbonate equivalent hardness or mg/lit.
PROCEDURE
1. Wash and dry all the apparatus cleanly with water.
2. Fill the burette with 0.01 M EDTA, remove the air bubble & adjust
the zerolevel on the burette. Attach the burette on the stand.
3. Pipette out 50 ml of sample no. 1 in the conical flask & to it add half test tube
of ammonia buffer & 1-2 drops of Eriochrome black T indicator.
4. Titrate the resulting wine-red solution against 0.01M EDTA from the
burette till the color changes to blue.
5. Repeat the same procedure with same sample & note down the constant
reading in the observation table.
6. In the similar way repeat the procedure and take the readings for other
samples.
7. Calculate the total hardness of given samples of water.
Chemical Equation:
OBSERVATIONS:
1. Solution in burette: 0.01M EDTA solution
2. Solution in conical flask: 50 ml of water sample + half test tube
ammonia buffer solution
3. Indicator: Eriochrome black T
4. End Point: Wine red to blue color.
OBSERVATION TABLE:
Sample no.1
Sample no.2
Observations Burette reading in ml CBR/MBR
I II II ml
Final
Initial
Difference
CALCULATIONS:
RESULTS:
The hardness of given samples is:
Hardness of sample no. 1 = mg/l
Hardness of sample no. 2 = ... mg/l
Experiment No. 2
Title: Acidity content of
Water
Date:
EXPERIMENT No. 2
ACIDITY OF WATER
PROCEDURE:
PART-I: PHENOLPHTHALEIN ACIDITY:
OBSERVATIONS:
PARTI: PHENOLPHTHALEIN ACIDITY
1. Solution in burette: N/50 NaOH solution
2. Solution in conical flask: 100 ml of water sample
3. Indicator: phenolphthalein
4. End Point: Colorless to pink
.
PARTI: METHYL ORANGE ACIDITY
1. Solution in burette: N/50 NaOH solution
2. Solution in conical flask: 100 ml of water sample
3. Indicator: Methyl Orange
4. End Point: orange to yellow
CALCULATIONS:
RESULTS
The Acidity of given samples is:
Phenolphthalein Methyl orange
Acidity (mg/litre) Acidity (mg/litre)
Experiment No. 3
Title: Alkalinity of Water
Date:
EXPERIMENT No. 3
ALKALINITY OF WATER
THEORY:
Total alkalinity is the measure of capacity of water to neutralize the strong acid.
The alkalinity is generally due to salts of carbonates, bicarbonates, phosphates,
nitrates together with OH ions in free solids. Total alkalinity can be measured by
titrating a water sample with strong acid (HC1) to pH 8.3 using phenolphthalein
as indicator & further to pH 4.2 to 5.4 with methyl orange indicator. In the first
case, the value is called as phenolphthalein alkalinity (PA) & in the second case,
the value is called as total, alkalinity (TA).
PROCEDURE:
1) Wash all the apparatus cleanly with water.
2) Fill the burette with 0.02 N HC1, remove the air bubble & adjust zero
level on the burette.
3) Take 100 ml of given water sample in the titration flask & add a drop of
NaOH solution to it.
4) Then add phenolphthalein indicator to this solution.
5) Titrtate the pink colored solution with 0.02 N HCl till the pink colour
disappears. Let this reading be A ml. (A1 for sample 1, A2 for sample 2 and A3
for sample 3.)
4) Now to the same solution which has become colorless, add 2 to 3 drops of
methyl orange indicator & continue the titration from same reading till the
yellow color changes to orange. This is total alkalinity (TA).
Let this reading be B ml. (B1 for sample 1 & B2, B3 for sample 2 and 3
respectively).
Course Code: 231FYP116 FY. B.Tech.
Applied Chemistry Lab. DYPSOEM
5) Calculate the phenolphthalein & total alkalinity for both the samples
OBSERVATIONS:
1 Solution in burette: 0.02 N HC1solution
2 Solution in conical flask: 100 ml of water sample + phenolphthalein +
Methyl Orange indicator
3 Indicator: phenolphthalein +Methyl Orange indicator
4 End Point: pink to colorless and yellow to orange
OBSERVATION TABLE:
Sample no.1
Sample no.2
Sample no.3
CALCULATIONS:
RESULTS:
The Alkalinity of given samples is:
Sample No. Phenolphthalein Methyl orange
Alkalinity (ppm) Alkalinity (ppm)
1
2
3
Experiment No. 4
Title: Chloride content of
Water
Date:
EXPERIMENT No. 4
CHLORIDE CONTENT OF THE WATER
PROCEDURE
1) Wash all the apparatus cleanly with water.
2) Fill the burette with 0.01 N AgNO3, remove the air bubble & adjust
zerolevel on the burette.
3) Pipette out 10 ccs of given water sample in the conical flask & to this sample
add 2 to 3 drops of K2CrO4, indicator. Titrate this solution with AgNO3, from
the t burette until reddish colour is obtained.
4) Note down this reading & repeat the same procedure to obtain a
constant burette reading.
5) In the similar manner, determine the burette reading for other water
samples.
Chemical Equation:
AgNO3 + Cl- AgCl + NO3-
OBSERVATIONS:
1) Solution in. burette: 0.01 N AgNO3,
2) Solution pipetted out: 10 cm3 water sample
3) Indicator used: K2CrO4
4) End point: Colorless to reddish color
Observation Table:
(Reading for distilled water Sample (A) =) 0.3 cm3)
Observations Burette reading in ml for CBR/MBR
Samples (B & C) ml (X)
(B) (C)
Final
Initial
Difference
CALCULATIONS:
[(𝑪 𝒐𝒓 𝑩) − 𝑨] 𝒙 𝟎. 𝟎𝟏 𝒙 𝟑𝟓. 𝟓 𝒙 𝟏𝟎𝟎𝟎]
𝐂𝐡𝐥𝐨𝐫𝐢𝐝𝐞 𝐜𝐨𝐧𝐭𝐞𝐧𝐭 =
𝟏𝟎
RESULTS
Sample B Sample C
Experiment No. 5
Title: PH Meter
(Demonstration Only)
Date:
EXPERIMENT No. - 5
DETERMINATION OF pH OF GIVEN SAMPLES USING pH METER
AIM: Determination of pH of Given water Samples using pH Meter
DIAGRAM
pH METER
Results:
Sr. PH of Solution Nature
No.
1
2
3
Experiment No. 6
Title: Colorimetric Method
(Demonstration Only)
Date:
EXPERIMENT NO. 6
ESTIMATION OF IRON CONTENT BY COLORIMETRIC
METHOD
Aim: To determine iron in a water sample by colorimetry.
Apparatus: Colorimeter, Volumetric flask (100ml), beaker (100ml).
Chemicals: Stock solutions of ferrous sulphate, distilled water, HCl, HNO3
Procedure:
1. Prepare a stock solution of ferrous sulphate and pipette out 10 mL in 100 mL
of volumetric flask.
2. Add 1 mL of concentrated HNO3 to flask, also add 5 ml of 40% ammonium
thiocyanate from a burette.
3. Dilute the above solution quantitatively to obtain 5, 10, 15.20,25 ppm
concentrations. Clean the absorption cell or sample tube
4. Switch on the instrument photo-colorimeter and warm up for it for 10
minutes. Adjust the filter position at 1 and the wave length at 495nm.
5. Fill the cuvette with blank (1%HCl) solution. Keep it in cell holder. Set the
filter at position 3 and find that absorbance is 0.00 reading.
6. Replace the blank sample tube with one of the test solutions from 1 to 5
and unknown. Read the absorbance for each sample solution.
7. Plot the graph of absorbance against concentration. It will be straight line.
From it find the concentration of unknown solution.
8. The above procedure is used for photo-colorimeter.
OBSERVATIONS:
CALCULATIONS:
Plot the graph of absorbance against the concentration. A linear
curve is obtained as shown. This shows that Beer-Lamberts law is
obeyed by the solution. Obtain the concentration of unknown
solution from the calibration curve.
Concentration of unknown solution = ------------ ppm.
RESULT:
Concentration of unknown solution = ------- ppm.
Experiment No. 7
Title: Preparation of Urea-
Formaldehyde polymer/resin
Date:
EXPERIMENT No. 7
PREPARATION OF UREA-FORMALDEHYDE POLYMER/RESIN
AIM: To prepare urea-formaldehyde polymer/resin
THEORY:
U-F resin are formed by condensation and polymerization of urea and
formaldehyde monomers; the mechanism is as follows
PROCEDURE:
OBSERVATIONS:
1. Weight of empty watch glass = W1 = ............gm
2. Weight of empty watch glass + polymer formed = W2 = ........... gm
3. Weight of polymer prepared (W) = W2 - W1 = ........... gm
RESULT:
Experiment No. 8
Title: Preparation of
Phenol-Formaldehyde resin.
Date:
EXPERIMENT NO. 8
Chemical Equation:
Step I: - Formation of ortho and para hydroxy benzyl alcohols from phenol and
formaldehyde: -
Procedure:
1) Place 5 ml of glacial acetic acid and 2.5 ml of formaldehyde solution in 500 ml
beaker.
2) Add 2 gm of phenol and 1 ml of conc. HCl solution in it.
3) Heat the solution slowly with constant stirring for 5 minutes.
4) A large mass of pink Plastic is formed.
5) The residue obtained is washed several times with distilled water.
6) Dry the product and calculate the yield accurately.
Observation:
1. Weight of empty watch glass = W1 = ................ gm
2. Weight of empty watch glass + polymer formed = W2 = ................. gm
3. Weight of polymer prepared (W) = W2 - W1 =................. gm
Results:
Experiment No. 9
EXPERIMENT NO: 9
AIM: To determine the proximate analysis of coal
APPARATUS:
1. Silica crucible with lid
2. weight balance
3. Muffle Furnace
4. Oven
SAMPLE REQUIRED: Powered coal sample (1gm)
ASH:
Coals are associated with certain mineral or inorganic matter, which gets deposited
along with vegetable matter or gets into coal by subsequent infiltration. The ash
consists mainly of silica, alumina, iron oxide and lime. When heated, coal as does
not melt sharply at any temperature, but begins to soften at much lower temperature
than that required melting. The ash content in coke is much higher than in coal.
PROCEDURE:
MOISTURE DETERMINATION:
1. Dry the silica dish in an oven and weigh.
2. Spread out about 1 gm of 20 mesh coal sample on the dish.
3. Weigh the dish again to find the exact mass of the sample.
4. Heat the dish without any cover in the oven at about 105-110 ℃ for 1 hour.
5. Take out the dish from the oven, cover it with the lid and cool.
6. Weigh the dish to find the loss in weight of coal due to presence of moisture.
ASH DETERMINATION:
1. Follow the steps 1 to 3 of moisture determination.
2. Insert the open dish in the furnace at 750 ℃ for an hour.
3. Remove the dish; allow it to cool for 10 minutes on the slab and 15 minutes in the
desiccators.
4. Weigh the dish to find the mass left which is the ash content of the coal.
Observations
Moisture
1) Weight of empty crucible (W1) =
2) Weight of empty crucible+ Wt. Of coal sample (W2) =
3) Weight of coal sample(W2-W1) =
Ash
1) Weight of empty crucible (W1) =
2) Weight of empty crucible+ Wt. Of coal sample (W2) =
3) Weight of coal sample(W2-W1) =
CALCULATION:
% of moisture in coal = (Loss in wt. of coal /wt. of coal initially taken) *100 %
% Ash in coal = (wt. of residue ash formed / wt. of coal initially taken) *100 %
Experiment No. 10
Date:
EXPERIMENT NO - 10
AIM: To determine the ultimate analysis of the coal sample.
SAMPLE REQUIRED: Powered coal sample (1gm).
THEORY:
1. Coal is composed primarily of carbon along with variable qualities of other
elements, like hydrogen, Sulphur, oxygen, nitrogen.
2. Ultimate analysis of coal, also known as elemental analysis, is the method of
determination of its total carbon, oxygen, nitrogen, Sulphur and ash content in the
given sample of coal.
3. Ultimate analysis is required as it is essential to understand the properties of bio
mass material to evaluate their utility.
4. As chemical food stock and also design suitable gasifier systems, the analysis is
carried out to fine oxygen required for combustion for efficient production of
energy.
5. It gives analysis in terms of elementary constituents and is helpful in combustion
calculation for design of furnaces and its auxiliaries.
PROCEDURE:
From the proximate analysis of coal, we have found that:
% of moisture = % (M)
% of ash content= % (A)
By using the above data of proximate analysis, the ultimate analysis of the supplied coal
sample i.e., the percentage of hydrogen, nitrogen, Sulphur, oxygen and carbon can be
calculated.
CALCULATION:
1. % of carbon content = 0.97(FC) +0.7(VM-0.1A)-M (0.6-0.01M)
2. % of hydrogen content = 0.036 (FC) + 0.086(VM-0.1A)-0.035M2
(1-0.02M)
3. % of Nitrogen content = 2.10-0.020(VM)
4. % of Sulphur content = 0.8%
5. % of oxygen content =100- (% C +% H+% N+% S)
Course Code: 231FYP116 FY. B.Tech.
Applied Chemistry Lab. DYPSOEM
CONCLUSION:
From the above experiment we have to find out the % of carbon content, % of
Hydrogen content, % of nitrogen content, % of Sulphur content and the % of
oxygen content of a given coal sample.
1 % of N =
2 % of S =
3 % of O =
4 % of C =
Course Code: 231FYP116 FY. B.Tech.
Applied Chemistry Lab. DYPSOEM
Experiment No. 11
Date:
Experiment No. 11
SYNTHESIS AND CHARACTERIZATION OF NANO-SIZED ZnO
AIM: Synthesis and Characterization of Nano-sized ZnO by precipitation method
Materials Required: Zinc nitrate hexahydrate (Zn(NO3)2.6H2O), 99 % , sodium
carbonate (Na2CO3), 99% and Ethanol (C2H5OH, 95%)
Procedure:
Synthesis of ZnO nanoparticle by Precipitation method Materials Zinc
nitrate as the precursor, KOH/NaOH as a precipitating agent to synthesize ZnO
nanoparticles Preparation ZnO nanoparticles can be synthesized by direct
precipitation method using zinc nitrate or zinc chloride and KOH or NaOH. The
aqueous solution (0.2 M) of zinc nitrate (Zn(NO3)2 6H2O) and the solution (0.4
M) of KOH to be prepared with deionized water, respectively. The KOH solution
should be added slowly into zinc nitrate solution (taken in a beaker) at room
temperature under vigorous stirring, which resulted in the formation of a white
suspension. The white product formed should be filtered and washed three times
with distilled water, and once with absolute alcohol. The obtained product to be
calcined at 180°C in hot air oven for 2 hr. The prepared ZnO nano particle to be
fine powder using mortar & pestle.
Characterization:
The optical properties of prepared ZnO NPs are analyzed by UV-visible
Spectrophotomet. A broad absorption peak is observed in each spectrum at 355-
380 nm which is a characteristic band for the pure ZnO. • The FT-IR shows a
broad absorption band related to Zn-O vibration band at 500 cm-1. • The SEM
results show the formation of spherical shaped nano particles.
Experiment No. 12
Title: Construction of Galvanic Cell.
Date:
EXPERIMENT NO. 12
Aim: Construction of a Galvanic cell
Required MATERIALS:
Chemicals
1. 0.5 M copper (II) sulfate
2. 0.5 M zinc sulfate
3. zinc, copper strips (approximately 1 cm x 10 cm)
Equipment
1. 100-mL beaker
2. Dialysis tubing
3. Hook-up wire or bell wire
4. 1.5-volt flashlight lamp with less than 100 milliamp rating
5. Alligator clamps
6. Crimping tool
7. Soldering iron and resin core solder
8. Clamps (for dialysis tubing)
9. Sandpaper or steel wool
PROCEDURE:
Prepare a test lamp by soldering wire test leads to a 1.5-volt flashlight lamp. Attach
alligator clips to the ends of the leads. Obtain strips of copper, each strip should be
2.5 cm longer than the height of the beaker being used. Sand the strips until they
are shiny. Tie a knot with string or use a non-reactive clamp in one end of dialysis
tubing that has been soaked in distilled water. The length of tubing should be long
enough so that it overlaps the edge of the beaker by 2.5 cm. Fill the dialysis tubing
with the prepared copper (II) sulfate solution. Place the copper strip in this piece
of dialysis tubing that is now filled with copper (II) sulfate solution and use string
or a rubber band to secure the top of the dialysis tubing around the copper. Leave
2.5 cm of copper sticking out of the tubing. Fill the beaker with the prepared zinc
sulfate solution; place both the dialysis tubing, containing the copper and copper
(II) sulfate solution, and the Zinc strip in the beaker. Secure both the zinc strip and
Course Code: 231FYP116 FY. B.Tech.
Applied Chemistry Lab. DYPSOEM
the copper strip in the dialysis tubing in the beaker by bending them over the edge
of the beaker. Complete the circuit by attaching one alligator clip to the copper
strip and the other to the zinc strip. Observe and record any activity taking place at
the metal strips, the solution (especially color changes), and the test lamp. Connect
several cells in series and operate a small radio or some other direct current
device. Try making cells with magnesium or aluminum in place of the zinc.
DISCUSSION
1. The following discussion applies when copper and magnesium strips are used
as the metal strips. If other metals are used, similar explanations can be used.
2. Zn(s) + Cu2+(aq) → Zn2+(aq) + Cu(s) + 1.1v
3. This reaction is an oxidation-reduction reaction in which the Zn is oxidized by
the copper to Zn2+ ions. The result of this reaction is a transfer of electrons which
provides the power required to light the flashlight lamp.
4. Students performing this experiment should be familiar with the following
terms: anode, cathode, oxidizing agent, reducing agent, and electromotive series.
Students should be presently studying a unit on electrochemistry and oxidation-
reduction reactions in order to fully understand the "chemistry" of this experiment.