Chapter 4
Chapter 4
Chapter 4
Tutor
Prepared By:
Priyanshu Pokhrel Asst. Prof. Shukra Raj Paudel
Rabin lamsal
Rabin Poudel Department Of Civil Engineering IOE,
Rahul Yadav
Rajan Bhushal Tribhuvan University
Rajesh shrestha
WHAT WILL STUDENTS LEARN AT
THE END OF THIS PRESENTATION !!
REMOVAL GOOD
IMPURE
OF
WATER WATER
PHYSICAL
IMPURITIES
HARMFU
CHEMICA L POTABLE
LLY SUBSTAN WATER
IMPURE CE
POTABLE WATER
CLASSIFICATION OF CLASSIFICATION OF
IMPURITIES ACCORDING IMPURITIES
TO ITS ACCORDING TO ITS
CHARACTERISTICS STATE
Physical Suspended
impurities impurities
Chemical Colloidal
impurities impurities
Bacteriologica Dissolved
l impurities impurities
Physical impurities
HARDNESS
ALKALINITY
RELATION BETWEEN HARDNESS AND ALKALINITY
NUMERICAL ON HARDNESS AND ALKALINITY
4.2.1 HARDNESS
Source:
chemicalprocessing.com
Types of hardness
A)temporary hardness
b)permanent hardness
a)temporary hardness
BOIL OR
HARDNESS
WATER ADDITION
REMOVED
OF LIME
B)Permanent hardness
Zeolite method
Source: ques10.com
Fig: permanent hardness
removal
source: quora
Source: slideshare.com
DETERMINATION OF
HARDNESS
TOTAL HARDNESS= CH + NCH
TOTAL ALKALINITY :
TOTAL ALKALINITY :
SOLUTION:
WE HAVE,
EQUIVALENT WT. OF CACO3 = 50
EQUIVALENT WT. OF CA = 20
TH> ALKALINITY
NCH = TH –CH
a)Aerobic
a)Cocci a)Saprophytic
b)Anaerobic
b)Bacilla b)parasitic
c)Facultative
c)spirilla
a)Psycrophillic
a)Pathogenic b)Mesophillic
b)Non-pathogenic c)Thermophillic
According to shape
Eg:-Malaria,
Water vector Diseases
Arboviruses, Filariasis
4.4.1 Water Borne Diseases
CHEMICAL CONTAMINATION:-
• Water borne chemical diseases are illness associated with ingestion
of water containing toxic substances in harmful concentrations. The
substances may be of natural origin or manmade and include metals
such as arsenic,iron, etc , inorganic chemicals such as fluoride, nitrate,
etc. And organic chemicals.
• In some cases, contamination of water is caused by industrial wastes
and drainage from fields containing harmful pesticides.
• It’s not major problem as microbiological diseases in context of nepal.
CHEMICAL CONTAMINATION
MICROBIOLOGICAL
CONTAMINATION
• It’s major part of our concern.
• Human faeces contaminate water supplies and trigger
a variety of diseases of microbiological nature.
Source:-medulance.com
CHOLER
A
Fig:-Bacterium Vibrio
Cholerae
• SOURCE: ABHIMANUIAS.COM
4.4.4 WATER VECTOR DISEASES
• The Diseases Which Are Transmitted By Insects Which Breed In Or Near Water
Are Called Water Vector Diseases.
• For Example:
1) Malaria
3)filariasis
WATER VECTOR DISEASES-
PROCESS OF TRANSMISSION
• The Transmission Of Diseases Involve At Least Three
Livimg Things-a Host(man And Animal), A Parasite
That Causes The Diseases(protozoa,virus Or Worm)
And A Carrier Or Vector(insect, Fly Or Mosquito).
• Transmission Occurs when Insect Becomes
Infected with Disease organism from Biting A Person
Or Animal , And Then Bites Another person.
• The parasites Are Injected Into The skin Of
Bloodstream By The Insect Bite, The Diseases
Being called Water Insect carried Diseases.
MALARIA
• Malaria Is An Infection Of Human By Protozoan
Transmitted Through Mosquito Bite.
• Symptoms Include Patient Feeling bad For No Specific
Reason Initially.
• Chills. Fever. Headaches, Nausea And Heavy Sweating
Follow Thereafter And The Cycle Is Repeated daily Or
Every several Days For Weeks, Months or Even Longer If
Not Treated.
• Relapses Are Common And May Occur Without Warning
For Many Years.
Arboviruses
, The Pulse Slows and Weakens, And The Blood Comes throuThe Arboviral
Diseases Transmitted By Mosquito Bite Include Yellow Fever And Dengue.
Yellow Fever Is Infectious Disease Of Short duration and The Attack May
Be Mild Or Severe.
Early Symptoms Of Yellow Fever Include Fever, Head And Body
Aches, nausea And Vomiting.
As The Disease Progressesgh nosebleed, Vomiting Or Stools.
Jaundice Is moderate Early But Becomes Severe later.
Dengue Has Similar Early Symptoms but Is Accompanied By A Rash ,
Recovering Patients suffer fatigue For Long Time.
Epidemics Of Disease are Explosive But Death Are Rare.
FILARIASIS
SOURCE: WHO(2019)
4.4.6 PREVENTIVE MEASURES
Identification Of Transmission Mechanism Is Helpful In
The Selection Of Suitable Preventive Measures.
The Barriers Should Be Employed In The transmission
Route to disrupt transmission Of Diseases.
Barriers Are Namely Primary And Secondary Barriers.
Primary Barriers are Employed By : A) washing Hands
With Soap After Defecation
B) constructing Sanitation Facilities to prevent the spread
of diseases.
PREVENTIVE MEASURES.....
• Secondary Barriers Are Hygiene Practices That Prevent
The fecal pathogens From Multiplying And Reaching The New Host
And These Are Employed By : A) washing Hands Before Food
B) cooking And Reheating food To Prevent survival And
Multiplication Of Pathogens.
• C) Protecting Water Supplies From Contamination
Through boiling Or chlorination.
• Other Secondary Barriers Include keeping Playgrounds Free From
Fecal Contaminants, preventing Children From Eating Earth And
Controlling Flies Etc
PREVENTIVE MEASURES....
2) Chemical
1)Physical 3)Bactoriological
Examination:
Examination :Don examination:
Done to determine
e to determine the Used to
the Chemical
physical determine the
impurities & their
impurities & their micro organism
characteristic
characteristic in the water
4.5.1 PHYSICAL EXAMINATION OF
WATER
Physical examination of water includes:
A) Temperature b) Color
C)Turbidity
Temperature :
Affects physical properties of water such as density, viscosity, surface tension
saturation value of gases etc.
Affects chemical and biological activity. At the lower temperature the rate if
the biological activity is lower and vice versa.
10°c to 15°c of water is desirable for drinking.
Determination Of Temperature In
Laboratory
Procedure:
Place the instrument in front of you with the
red switch towards you.
Open the lid at the top of the instrument.
Insert the color measurement disc (Hazen
disc).
Place an empty glass tube in the left hand slot.
Fill the other tube with the water sample and Fig: Tintometer
𝑐𝑜𝑛𝑐𝑒𝑛𝑡𝑟𝑎𝑡𝑖𝑜𝑛𝑜𝑓𝑎𝑛𝑖𝑜𝑛𝑠𝑋𝑐𝑜𝑛𝑐𝑒𝑛𝑡𝑟𝑎𝑡𝑖𝑜𝑛𝑜𝑓𝑐𝑎𝑡𝑖𝑜𝑛𝑠
Constant
𝑐𝑜𝑛𝑐𝑒𝑛𝑡𝑟𝑎𝑡𝑖𝑜𝑛𝑜𝑓𝑢𝑛𝑑𝑖𝑠𝑠𝑜𝑐𝑖𝑎𝑡𝑒𝑑𝑚𝑜𝑙𝑒𝑐𝑢𝑙𝑒𝑠
• [H+] X [OH-] = Ionization constant
• HERE,
• Ionization constant = 10^(-14) AT 21°C.
• PH=LOG(1/[𝐻+])
Determination Of pH In Laboratory
• PROCEDURE:
Pour some pH 4 buffer solution into one the 100ml beakers.
Take the temperature of the solution.
Set this temperature on the dial of the meter.
Switch on the meter and set into “pH manual”.
Remove the electrode form the beaker in which it is stored and wash it
down with de-ionised or distilled water.
Place the electrode in the buffer solution.
The meter should read pH 4.
If the meter does not read pH 4 use the knob marked “buffer to set the
reading to pH 4”.
Remove the electrode form the buffer and wash it down with deionised or
distilled water.
Pour some of the water sample into 250 ml beaker.
Wash down the electrode and place it in the sample.12.Record the pH value
SOLID
Solid present in the water are either in dissolved solid or
suspended solid.
The total solid is the sum of the dissolved solid and the
suspended solid.
Dissolved solid result from the solvent action of the water.
Dissolved solid may be inorganic salts, minerals, organic
matters.
Suspended particle may consist of the organic and
inorganic matters.
DETERMINATION OF SOLID IN
LABORATORY
(A)To measure the suspended solids in sample of sewage
• Procedure:
Weigh the membrane filter circle accurately = A gm.
Fix the circle in the filter holder.
Measure the volume of the sample sewage. A volume of 50 ml to be
measured for raw sewage.
Transfer the sample to the funnel and vacuum the filter.
Carefully, transfer the filter circle to the drying oven and dry for 30
minutes at 105oc.
Remove the circle form the oven and cool it in a dessicator.
Re-weight =B gm. Suspended solid content in the original
sample(mg/l) = (B-A) X 1000/vol. Of water used (50 ml)
• (B)To determine the amount of total solids in given sample
• procedure:
Place a clean evaporating dish in the drying oven at 105oc, for 30
minutes.
Weigh the dish , W = A gm
Measure 50 ml of water sample with the help of a pipette and transfer to
the evaporating dish.
Put the dish on the burner and evaporate it to dryness.
Put it to the drying oven for 10 minutes.
Remove the dish from the oven and place in the desiccator to cool for 5
minutes.
Weigh the dish + residue, W = B gm total solids = 2 X (B –A) X 104mg/l.
Compare your value with the WHO standards.
4.5.3 BACTERIOLOGICAL
EXAMINATION
Here, in this examination, the concentration of coliforms and E-
coli are tested rather than pathogens because they are small in
numbers and their testing is time consuming and expensive.
There are two methods of determining coliform and E-coli in the
lab:
➢Multiple tube fermentation technique
➢Membrane filter fermentation technique
MULTIPLE TUBE
FERMENTATION TECHNIQUE
yes
Proceed to next yes
test Proceed to
Results in all tubes next test
positive
N Observe
Continue same Sample with
o Gas in
test for another negative
tubes
24 hours result are
N discarded
Confirmed Test
➢Except coliforms, other bacteria may also ferment lactose broth
and produce gas.
➢This test thus confirms the result with more degree of accuracy.
➢Consists of growing cultures of coliform group of bacteria on
media which suppress the growth of other organisms.
• Procedure
Yes Test is
Samples from Presumptive
positive
test transferred to fermentation
Observe Gas
tubes containing brilliant
in tubes
green lactose broth at temp
37°Cfor 24 hours
• No Test is
negative
yes
Proceed to yes
Proceed to
next test
Results in all tubes next tes
positive
N Observe
o Continue same
Gas in
test for another Sample with
tubes
24 hours negative result
N are discarded
Completed Test
Demonstrates certainly that the organisms showing
positive results in the confirmed tests are members of
coliform group.
• Procedure
Yes Test is
Discrete
Positive result sample from positive
isolated
confirmed test placed in Eosin colonies at
methylene blue agarfor 37°C& 37°Cfor 24
24 hours. hours
• No Test is
negative
yes
yes Test is
End all test
positive. End
Results in all tubes all Tests
positive
N Observe
o Continue same
Gas in
test for another Sample with
tubes
24 hours negative result
N are discarded
Most Probable Number
3 of 1 3 of 0.1
3of 10 ml each ml each ml each MPN Index lower Upper
0 0 1 3 <0.5 9
0 1 0 3 <0.5 13
1 0 0 4 <0.5 20
1 0 1 7 1 21
1 1 0 7 1 23
1 1 1 11 3 36
1 2 0 11 3 36
2 0 0 9 1 36
2 0 1 14 3 37
2 1 0 15 3 44
2 1 1 20 7 89
2 2 0 21 4 47
2 2 1 28 10 150
3 0 0 23 4 120
3 0 1 39 7 130
3 0 2 64 15 380
3 1 0 43 7 210
3 1 1 75 14 230
3 1 2 120 30 380
3 2 0 93 15 380
3 2 1 150 30 440
3 2 2 210 35 470
3 3 0 240 36 1300
3 3 1 460 71 2400
(B) Membrane filter fermentation technique
NDWDQS WHO++
Turbidity NTU 5(10)** 5
pH 6.5-8.5** 6.5-8.5*
Colour TCU 5(15)* 5
Taste and Odor Would not be
objectionable
Total dissolved solid mg/l 1000
Electrical conductivity µc/cm 1500
Iron mg/l 0.3(3)** 0.3
Manganese mg/l 0.2 0.1
Arsenic mg/l 0.05 0.01
Cadmium mg/l 0.003 0.003
Chromium mg/l 0.05 0.05
Cyanide mg/l 0.07 0.07
Fluoride mg/l 0.5-1.5* 1.5
Lead mg/l 0.01 0.01
Ammonia mg/l 1.5 1.5
Chloride mg/l 250 250
Sulphate mg/l 250 250
Calcium mg/l 25
Magnesium mg/l 20
Sodium mg/l 150
Potassium mg/l 12
Nitrate mg/l 50 10
Nitrite mg/l 0.01
Copper mg/l 1 2
Total Hardness mg/l 500 500
Total Alkalinity mg/l 500
Calcium mg/l 200 25
Zinc mg/l 3 3
Nickel mg/l 0.02
Barium mg/l 0.7
Boron mg/l 0.3
Mercury mg/l 0.001 0.001
Uranium mg/l 0.002
Aluminium mg/l 0.2 0.2
Residual Chlorine mg/l 0.1-0.2*
E-Coil MPN/l 0 0
Total Coliform MPN/l 95% in sample 0