Section I Introduction - Philadelphia University materi… · is produced per day? Answer 0.2 *...
Transcript of Section I Introduction - Philadelphia University materi… · is produced per day? Answer 0.2 *...
Section I Introduction
1
Environmental Engineering (0670343)
Very Important Note: Most of the figures and tables are downloaded from google
and various text books
System Units:
1- International system (SI)
is the modern form of the metric system.
It is the world's most widely used system of units, both in everyday commerce
and in science.
The SI was developed in 1960 from the metre-kilogram-second (mks) system,
rather than the centimetre-gram-second (cgs) system which, in turn, had many
variants.
2- Non SI unit like U.S. and UK
In the United States, industrial use of SI is increasing, but popular use is still limited.
In the United Kingdom, conversion to metric units is official policy but not yet
complete. Those countries that still recognize non-SI units (e.g. the U.S. and UK)
have redefined their traditional non-SI units in terms of SI units.
Basic SI Units
Type Name Symbol
length metre m
mass kilogram kg
time second s
electric current ampere A
temperature kelvin K
amount of substance mole mol
luminous intensity candela cd
Section I Introduction
2
SI prefixes
Factor Prefix Symbol
1024
1E24 yotta Y
1021
1E21 zetta Z
1018
1E18 exa E
1015
1E15 peta P
1012
1E12 tera T
109 1E9 giga G
106 1E6 mega M
103 1E3 kilo k
102 1E2 hecto h
101 1E1 deca da
101 1E1 deka da
10-1
1E-1 deci d
10-2
1E-2 centi c
10-3
1E-3 milli m
10-6
1E-6 micro µ
10-9
1E-9 nano n
10-12
1E-12 pico p
10-15
1E-15 femto f
10-18
1E-18 atto a
10-21
1E-21 zepto z
10-24
1E-24 yocto y
What to remember:
1ft = 12inch
1 inch = 2.54 cm
1 ft = 30.48 cm
Section I Introduction
3
1 US gallon = 3.78L
1 mile = 1609 m
I pound = 454g
Example:
Some employees at GE wash the PCB tainted floor with organic solvent (TCE) and
the discharge enters a holding tank that is 25 m x 25 m x 5 ft and is full with water.
The volume of solvent is 3 L and the concentration of PCBs in the solvent is 10 ppm.
What is the final concentration of PCB in mg/l in the holding tank?
Solution:
Tank Volume = 25*25*5*0.3048 = 937.5m3
Added solvent quantity (gramm) = 3L*10 mg/L = 30mg = 0.03g
The final concentration (mg/l) = 30/(937500+3) = mg/l
Reactor and Material balance:
Law of matter conservation: the matter can neither be created or destroyed
Law of Energy conservation: the energy can neither be created or destroyed but it
transformed form one type of energy to another
Material Balance:
- Is a key tools in achieving a quantitative understanding of the behavior of
environmental systems.
- It provide us with a tool for modeling the production, transport, and fate of
pollutants in the environment
Main equation:
Accumulation = input – output
- The control volume: it is a imaginary line around the process flowchart or part
of it in which the inputs, outputs and accumulations are determined to ease the
problem solution.
Section I Introduction
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Example: a family brings approximately 50 kg of consumer good a week (food,
magazine , appliances…) of this amount 60% is consumed as food . half of the food is
used for biological maintenance and ultimately released as CO2 and the reminder is
discharged to sewer. The green recycle is about 25% of the solid waste that is
generated. Approximately 1kg is accumulated at home. Estimate the solid waste
amount that placed at curb each week??
consumer good food
(input)
Solid waste
Consumed food = 0.6 * 50 = 30 kg
Input = output (food) + output (solid waste) + accumulation
50 = 30 + solid waste + 1 total amount of generated solid waste = 19 kg
25% of the solid waste is recycled = 0.25 * 19 = 4.75 kg is recycled
Thus the solid waste send to curb side collection weekly = 19- 4.75 = 14.25 kg.
Time factor:
Mass rate of input = mass rate of output + mass rate of accumulation
𝑑𝑚𝑎𝑠𝑠𝑖𝑛𝑝𝑢𝑡
𝑑𝑡=
𝑑𝑚𝑎𝑠𝑠𝑜𝑢𝑡𝑝𝑢𝑡
𝑑𝑡+
𝑑𝑚𝑎𝑠𝑠𝑎𝑐𝑢𝑢𝑚𝑢𝑙𝑎𝑡𝑖𝑜𝑛
𝑑𝑡
Example:
a tank with volume 0.35 m3 has a leak, the inlet tap flows water at rate 2.32 L/min
while the leak (outlet) is running at 0.32 L/min of water. how long it takes to fill the
tank? How much water has been wasted?
𝑑(𝑖𝑛)
𝑑𝑡=
𝑑(𝑜𝑢𝑡)
𝑑𝑡+
𝑑(𝑎𝑐𝑐𝑢𝑚𝑢𝑙𝑎𝑡𝑖𝑜𝑛)
𝑑𝑡
Accumulation
Section I Introduction
5
𝑑(𝑎𝑐𝑐𝑢𝑚𝑢𝑙𝑎𝑡𝑖𝑜𝑛)
𝑑𝑡= 2.32 – 0.32 = 2L/min
The tank volume = 0.35 m3 = 350 L
The time needed to fill the tank = 350 𝐿
2 𝐿/𝑚𝑖𝑛= 175 𝑚𝑖𝑛
The amount of wasted water = 175 min * 0.32 l/min = 56 L.
Efficiency = (𝒊𝒏−𝒐𝒖𝒕
𝒊𝒏) × 𝟏𝟎𝟎%
Example:
a waste incinerator has an air pollution control bag filter to collect the particulate
matter. The bag filter consists of 424 cloth bags arranged in parallel.where 1/424 of
the flow goes through each bag. The gas flow rate in and out of the filter is 47m3/sec.
and the concentration of the particulate entering the filter is 15g/m3. Under normal
operation the bag filter meets the authority discharge requirement of 24mg/m3
?estimate the removed particle in kg? estimate the efficiency of the bag filter? if due
to emergency one cloth bag is damaged and getout of the service, dose the effluent
comply with the standard?
Air inFlow Q= 47m3/sec out flow = 47m
3/sec
Cin= 15g/m3
Cout= 24mg/m3
Particulate removed by filter??
𝑑(𝑖𝑛)
𝑑(𝑣𝑜𝑙𝑢𝑚𝑒)=
𝑑(𝑜𝑢𝑡)
𝑑(𝑣𝑜𝑙𝑢𝑚𝑒)+
𝑑(𝑎𝑐𝑐𝑢𝑚𝑢𝑙𝑎𝑡𝑖𝑜𝑛)
𝑑(𝑣𝑜𝑙𝑢𝑚𝑒)
Note: the accumulated particulate is discharged as waste.
Concentration of inlet particulate =
15000 𝑚𝑔
𝑚3×
47 𝑚3
𝑠𝑒𝑐= 705,000 mg/sec
Section I Introduction
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Outlet concentration =
24 𝑚𝑔
𝑚3×
47 𝑚3
𝑠𝑒𝑐= 1800 mg/sec
1- Removed particle = 705,000 – 1,800 = 703,872mg/sec = 0.7038 kg/sec
2- Efficiency = (15000 – 24 / 15000)*100% = 99.84%
Or
Efficiency = (705000 - 1800 / 705000 )*100% = 0.9984
3- Since the flow is distributed over the bag clothes
Q =(1
424) 47𝑚3/sec
Bypass
Air in-Flow Q= (423
424) *47m
3/sec out flow = (
423
424) 47m
3/sec
Cin= 15g/m3
Cout= ??
Particulate removed by filter??
- Then Concentration of Bypass = 15000 *1
424 * 47 = 1,662.7 mg/sec
- The inflow = 15000 𝑚𝑔
𝑚3 ×423
424× 47
𝑚3
𝑠𝑒𝑐 = 703,337.2 𝑚𝑔/𝑠𝑒𝑐
- The efficiency of the bag filter is constant = 99.84%
- Thus the removed particulate by filter = 0.9984 × 703,337.2 𝑚𝑔/ sec =
702,211.9
- Then the amount of particulate left the system = in – out
- = 703,337.2 𝑚𝑔/ sec − 702,211.9 = 1,125.2 𝑚𝑔/𝑠𝑒𝑐
Thus the total outlet concentration = out from bypass + filter outflow
= 1,662.7 mg/sec + 1,125.2 𝑚𝑔/ sec = 2,787.9 𝑚𝑔/𝑠𝑒𝑐
Section I Introduction
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The overall concentration in the effluent = 2,787.9 𝑚𝑔/𝑠𝑒𝑐
47 𝑚3 /𝑠𝑒𝑐= 59.3 𝑚𝑔/𝑚3
The new efficiency = 115000−59
15000× 100% = 99.61%
Example:
A wastewater treatment plant with an output of 38400m3/day discharges the liquid
effluent with a BOD of 20mg/L into a river. If the BOD of the river upstream of the
discharge point is 0.2mg/l, at a minimum flow of 20m3/s, compare the BOD of the
river downstream of the discharge, assuming complete mixing?
Discharge amount = 20𝑚𝑔
𝐿× 38400
𝑚3
𝑑𝑎𝑦∗ 1000
𝐿
𝑚3 = 768 kg/day = 8888mg/sec
River flow = 0.2g/m3 *
20 𝑚3
𝑠𝑒𝑐 = 4g/sec
Plant discharge = 38400 m3/day = 0.44 m
3/sec
Thus the final concentration downstream = 4000𝑚𝑔
𝑠𝑒𝑐 + 8888
𝑚𝑔
𝑠𝑒𝑐/(20,000 + 440) l/sec
= 0.64mg/l
Example:
A slurry containing 20 percent by weight of limestone (CaCO3) is processes to
separate pure dry limestone from water. If feed rate of the slurry is 2000kg/h, how
much CaCO3 is produced per day?
Answer 0.2 * 2000 = 400 kg/h = 400*24 = 9,600 kg/day
HW#1:
1. Each day 3780 m3 of wastewater is treated at a municipal wastewater
treatment plant. The influent contains 220 mg/L of suspended solids. The
clarified water has a suspended solids concentration of 5mg/L. Determine the
mass of sludge produced daily from the clarifier and write down the mass
balance of the clarifier.
Answer (215g/m3
*3780m3/day = 812.7 kg/day)
Section I Introduction
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Section II Reactors
9
Reactor and steady state:
in most of environmental system a transformation occurs within the system and by
product is formed (CO2; bio-mass formed…)
Accumulation rate = input rate – output rate ±𝑡𝑟𝑎𝑛𝑠𝑓𝑜𝑟𝑚𝑎𝑡𝑖𝑜𝑛 𝑟𝑎𝑡𝑒
𝑑𝑀
𝑑𝑡=
𝑑(𝑖𝑛)
𝑑𝑡−
𝑑(𝑜𝑢𝑡)
𝑑𝑡 + 𝑟 …… (**)
Where r is the rate of reaction that is a complex function of pressure, temperature and
reactants and products concentrations.
Analysis performance of reactor type
Reactor Types:
1- Batch reactor
2- Continuous flow stirred tank reactor (CSTR)
3- Plug flow reactor (PFR)
1- Batch reactor :
- There is no in or out (it is like domestic mixer) fill in the material ,
- Mix and allow time for reaction to occur then discharge.
- Most experiment done in such reactor, because it is cheap, easy to operate and
build
𝑑𝑀
𝑑𝑡=
𝑑(𝑖𝑛)
𝑑𝑡−
𝑑(𝑜𝑢𝑡)
𝑑𝑡 + 𝑟
influent Effluent
Qin
CAin
Q out
C Aout
V (m3)
Reactor
Section II Reactors
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In this reactor 𝑑(𝑖𝑛)
𝑑𝑡=
𝑑(𝑜𝑢𝑡)
𝑑𝑡= 0 , and M = C.V
Thus the main reaction equation is (**)
𝑑𝑀
𝑑𝑡= 𝑉
𝑑𝐶
𝑑𝑡= 𝑟 𝑉
𝑑𝐶
𝑑𝑡= −𝑘𝐶𝑉
𝑑𝐶
𝑑𝑡= −𝑘𝐶 𝑙𝑛
𝐶𝑜𝑢𝑡
𝐶𝑖𝑛 = −𝑘t
Example:
a contaminated soil is to be excavated and treated in a completely mixed
aerated lagoon. How long time it is needed to treat the soil. If the
following data obtained from lab scale batch reactor, assume first order
reaction. Estiamte the reaction constant k? and the required time to
achieve reduction of 99% of the original concentration?
Tiem (day) Waste concentration (mg/l)
1 280
16 132
Solution:
During 15 days (16-1) the waste concentration decreased from 280-132
Using the (**) equation
𝑑𝑀
𝑑𝑡= 𝑟 = −𝑘𝐶
𝑑𝐶
𝑑𝑡= −𝑘𝐶
𝐶𝑡
𝐶𝑜= 𝑒−𝑘 (15)
Section II Reactors
11
𝑙𝑛 132
280= −15 × 𝑘
K = 0.0501 d-1
thus to achieve 99% reduction: 𝐶𝑡
𝐶𝑜 = 0.01
then ln(0.1) = 0.0501 (t) t = 91.9 day = 92 day
What dose it mean??
No material in or out
Section II Reactors
12
2- CSTR: or equilization basin
𝑑𝑀
𝑑𝑡=
𝑑(𝑖𝑛)
𝑑𝑡−
𝑑(𝑜𝑢𝑡)
𝑑𝑡 + 𝑟
Where M = CV
Then the equation (**) become
𝑉𝑑𝐶
𝑑𝑡= 𝐶𝑖𝑛𝑄𝑖𝑛 − 𝐶𝑜𝑢𝑡𝑄𝑜𝑢𝑡 − 𝑘𝐶𝑜𝑢𝑡𝑉
For completely mix Qin = Qout, and divide by tnak volme (𝑉)
Residence time (to)= V/Q
𝑑𝐶
𝑑𝑡=
𝐶𝑖𝑛
𝑡𝑜−
𝐶𝑜𝑢𝑡
𝑡𝑜− 𝑘𝐶𝑜𝑢𝑡
for stedy state dc/dt = 0
Section II Reactors
13
𝐶𝑖𝑛
𝑡𝑜=
𝐶𝑜𝑢𝑡
𝑡𝑜+ 𝑘𝐶𝑜𝑢𝑡
𝐶𝑖𝑛
𝑡𝑜= 𝐶𝑜𝑢𝑡 (
1
𝑡𝑜 + 𝑘)
𝐶𝑜𝑢𝑡 = 𝐶𝑖𝑛
1 + 𝑘𝑡𝑜
Section II Reactors
14
Section II Reactors
15
Example:
A sewerage lagoon with surface area = 10 ha and water depth of 1m. The lagoon
receive daily waste water = 430 m3/day with pollutant concentration = 180 ppm. The
pollutant degradation in the lagoon is according the first order reaction with K = 0.7
day-1
find the concentration of the effluent ?
Solution: Assume
1- The lagoon is completely mixed
2- Their is no water losses
3- And steady state
𝑑𝑀
𝑑𝑡=
𝑑(𝑖𝑛)
𝑑𝑡−
𝑑(𝑜𝑢𝑡)
𝑑𝑡 + 𝑟
𝑉𝑑𝐶
𝑑𝑡= 𝐶𝑖𝑛𝑄𝑖𝑛 − 𝐶𝑜𝑢𝑡𝑄𝑜𝑢𝑡 − 𝑘𝐶𝑜𝑢𝑡𝑉
For completely mix Qin = Qout, and divide by tnak volme (𝑉)
Residence time (to)= V/Q
𝑑𝐶
𝑑𝑡=
𝐶𝑖𝑛
𝑡𝑜−
𝐶𝑜𝑢𝑡
𝑡𝑜− 𝑘𝐶𝑜𝑢𝑡
Section II Reactors
16
for stedy state dc/dt = 0
𝐶𝑜𝑢𝑡 = 𝐶𝑖𝑛
1 + 𝑘𝑡𝑜
Tank volume = 10 *104 (m
2) * 1m = 10,000 m
3
residence time at the tank (to) = V/Q = 100,000/(430) = 232.558 day
Cout = 180 / (1+ 0.7*232.558) = 1.09 mg/l
Example 2 : CSTR
Before entering the underground utility to do a maintenance, the air sample was
analyzed and found to contain 29 mg/m3 of H2S. The maximum allowable exposer
limit is 14 mg/m3. Thus the worker ventilate vault (القبو) using an air blower that has a
flow of 10 m3/min. if the vault volume is 160 m
3 estimate how long time it is required
to lower H2S concentration to the allowable limit?
Assume the vault behaves as CSTR and the H2S is non-reactive?
The general MB equation is
𝑑𝑀
𝑑𝑡=
𝑑(𝑖𝑛)
𝑑𝑡−
𝑑(𝑜𝑢𝑡)
𝑑𝑡 + 𝑟
But since no inlet and no reaction (non reactive)
𝑑𝑀
𝑑𝑡= −
𝑑(𝑜𝑢𝑡)
𝑑𝑡
V𝑑𝑐
𝑑𝑡= −𝑄𝑜𝑢𝑡𝐶𝑜𝑢𝑡
But the residence time τ = V/Q
Ct = Co Exp(-t/τ)
where
Section II Reactors
17
Ct : is the concentration at any time
Co : is the initial concentration
We need to calculate the residence time
τ = 160 𝑚3
10 𝑚3/𝑚𝑖𝑛 = 16 min
Now the required time is
14 𝑚𝑔/𝑚3
29𝑚𝑔
𝑚3
= exp (-t/ 16)
Thus the required time t = 11.6 min
Note: the H2S threshold is 0.18 mg/m3 thus the vault will keep have a very strong
odor (ad smell) even after 12 min of blowing
Concentration
(ppm)
Symptoms/Effects
0.00011-
0.00033
Typical background concentrations
0.01-1.5 Odor threshold (when rotten egg smell is first noticeable to some). Odor becomes
more offensive at 3-5 ppm. Above 30 ppm, odor described as sweet or sickeningly
sweet.
2-5 Prolonged exposure may cause nausea, tearing of the eyes, headaches or loss of
sleep. Airway problems (bronchial constriction) in some asthma patients.
20 Possible fatigue, loss of appetite, headache, irritability, poor memory, dizziness.
50-100 Slight conjunctivitis ("gas eye") and respiratory tract irritation after 1 hour. May
cause digestive upset and loss of appetite.
100 Coughing, eye irritation, loss of smell after 2-15 minutes (olfactory fatigue).
Altered breathing, drowsiness after 15-30 minutes. Throat irritation after 1 hour.
Gradual increase in severity of symptoms over several hours. Death may occur
after 48 hours.
Section II Reactors
18
100-150 Loss of smell (olfactory fatigue or paralysis).
200-300 Marked conjunctivitis and respiratory tract irritation after 1 hour. Pulmonary
edema may occur from prolonged exposure.
500-700 Staggering, collapse in 5 minutes. Serious damage to the eyes in 30 minutes.
Death after 30-60 minutes.
700-1000 Rapid unconsciousness, "knockdown" or immediate collapse within 1 to 2 breaths,
breathing stops death within minutes.
1000-2000 Nearly instant death
Source : OSHA (US department of labor)
3- PFR:
it can be represented as a pipe or long river.
- Biological treatment of domestic waste water (WW) usually done in long
narrow tank that may modeled as PFR
𝑑𝑀
𝑑𝑡=
𝑑(𝑖𝑛)
𝑑𝑡−
𝑑(𝑜𝑢𝑡)
𝑑𝑡 + 𝑟 …… (**)
But because no mass excange accure during the flow in the pipe
d(in) and d(out) = 0
Thus the equation (**) became as batch reactor
𝑑𝑀
𝑑𝑡= 𝑟 𝑉
𝑑𝐶
𝑑𝑡= −𝑘𝐶𝑉
𝑑𝐶
𝑑𝑡= −𝑘𝐶 𝑙𝑛
𝐶𝑜𝑢𝑡
𝐶𝑖𝑛= −𝑘t
Another form of the equation:
t= is the travel time and equalt L/U
where
L: length of plug-flow segment
Section II Reactors
19
U: is the Linear velocity, m/s
In (Cout/Cin)=-K L/U= -k V/Q
Example:
(exam): a waste water plant needs to disinfect its effluent , the treated water contains
4.5 × 105 fecal coliform colony forming unit (CFU) per liter. But the maximum
allowable concentration is 2000 CFU per liter. If the pipe is used to carry the water,
determine the required pipe length if the water flow inside the pipe by 0.75m/sec. and
the reaction rate constant for fecal coliform destruction is 0.23 min-1
Solution: assume that the pipe behave a s steady state plug flow reactor and the
reaction rate is first order:
ln𝐶𝑜𝑢𝑡
𝐶𝑖𝑛 = −𝑘𝑡 ln
2000
4.5 × 105= −(0.23)𝑡
Required residence time (t) = 23.5 min = 1,412.9 sec
But t = 𝑣𝑜𝑙𝑢𝑚𝑒 (𝑉)
𝑄 =
𝐴𝑟𝑒𝑎∗𝐿
𝑣∗𝐴𝑟𝑒𝑎= 𝐿/𝑣
0.75 m/sec * 1412.9 = 1059.7 = 1060 m
Section II Reactors
20
General Material Balance equation for first order reaction rates:
influent Effluent
Qin
CAin
Q
out
C Aout
V (m3)
Reactor
Section II Reactors
21
VdC/dt =ΣCinQin − ΣCoutQout±kCV
C = concentration in the control volume (river/stream/reactor) [=] mg/L
V = volume of control volume [=] L, m3, ft
3
Qin = flowrate of inlet streams [=]m3/s, L/s, cfs, MGD
Qout = summation of all outlet streams
[=]m3/s, L/s, cfs, MGD
Cin = concentration in each inlet stream [= ] mg/L
Cout = concentration in each inlet stream [= ] mg/L
k = 1st order reaction rate constant (will be given) [=] 1/s
t = time [=] sec, mi
Section III Water Chemistry
22
Water Quality: Introduction
Very Important Note: Most of the figures and tables are downloaded from google
and various text books
It is a branch of Civil engineering deals with study, design and construct of drinking
and waste water plant and their network. It consists of
a- Water supply engineering: it deals with drinking water (collection, treatment,
storage and distribution)
b- Waste water engineering: deals with domestic and industrial waste water
(collection, treatment and disposal)
c- Environmental Engineering: deals with pollutant and their reduction, treatment
and disposal.
water uses are
Drinking, removing, or diluting wastes, agriculture, producing and goods
manufacturing and energy production
Required water quantity depends on various factors:
I. climatic conditions,
II. Extreme weather
III. lifestyle and city size
IV. Culture and tradition: and activities within the community.
V. Diet and population characteristics
VI. technology,
VII. and wealth
Section III Water Chemistry
23
Source of water:
Chemistry: Review:
Molecular weight: is the mass of a molecule. It is a sum of the combining element
[g/mole].
Equivalent weight: is the molecular weight divided by the number of positive or
negative electrical charges that resulting from compound dissolution [g/eq. weight]
Molarity (M): [No. of mole/L]: is the number of mole per litter of solution
Molality [mole/kg]is the number of mole per kg of material
Normality (N) [g equ./l]: is the number of equivalent weight per litter of solution
It is N = M*n
ppm : part per million and equals to mg/l
Fe2 (SO4)3 has a MW = 400 [g/mole]
-since its dissolution produces 6 charge
thus its eq. weight = 400/6 = 66.7 [g/eq. weight]
Section III Water Chemistry
24
Examples:
(1) H2SO4 + 2OH-= 2H2O + SO4
2-
Molecular weight of sulfuric acid (H2SO4) = (2*1) + (1*32) + (4*16) = 98.07 g/mol
Equivalent weight of sulfuric acid (H2SO4) = 49.03 g/equivalent of H+
Reasoning:
98.07 g/mol H2SO4 * (1 mole H2SO4 / 2 equivalents of H+) = 49.03 g/equivalent of H
+
In this example, the magnitude of the equivalent weight of sulfuric acid is HALF of
that of the molecular weight. This is because according to the balanced chemical
reaction, one mole of sulfuric acid reacts with TWO equivalents of hydroxide.
Example 2:
NH4OH + H+ = H2O + NH4
+
Molecular weight of ammonium hydroxide (NH4OH) = 35.00 g/mol
Equivalent weight of ammonium hydroxide (NH4OH) = 35.00 g/equivalent of OH-
Reasoning:
35.00g/mol of NH4OH * (1 mole NH4OH / 1 equivalent of OH-) = 35.00 g/equivalent
of OH-
In this example, the magnitude of the equivalent weight of ammonium hydroxide is
the same as the molecular weight.This is beacuse according to the balanced chemical
reaction, one mole of ammonium hydroxide reacts with ONE equivalent of H+.
Example 3:
Calculate the equivalent weights of HNO3 (MW = 63) and Ga(OH)3
(MW = 121) in the following three reactions:
- (a) 3HNO3 + Ga(OH)3 → 3H2O + Ga(NO3)3
EW(HNO3) = 63/1 = 63g
EW[Ga(OH)3] = 121/3 = 40.3g
Section III Water Chemistry
25
All 3 OH- enter the reaction. Note the 3 water formed and that no unused OH
- are
found in the salt Ga(NO3)3.
- (b) HNO3 + Ga(OH)3 → H2O + Ga(OH)2(NO3)
EW(HNO3) = 63/1 = 63g
EW(Ga(OH)3] = 121/1 = 121g
Since only 1 H+ is available to react with the 3 OH
- from the Ga(OH)3, only 1 OH
-
reacts. Note also that only one water forms and two OH- are left unused in the salt
Ga(OH)2NO3.
- (c) 2HNO3 + Ga(OH)3 → 2H2O + Ga(OH)(NO3)2
EW(HNO3) = 63/1 = 63g
EW[Ga(OH)3] = 121/2 = 60.5g
Two OH- are used by the 2H
+ provided by the 2 moles of HNO3. Note also that 2
moles of water form and 1 OH- is left unused in the product Ga(OH)(NO3)2.
Example:
500 mg of anhydrous Ca(HCO3)2 is dissolved in 750 ml of water. What is the molar
concentration, normality and the concentration in ppm as expressed as CaCO3?
Mw of Ca(HCO3)2 = 162gm/mole
The equivalent weight = 162/2 = 81g/equivelant
Concentration of Ca(HCO3)2 in the solution = 500/0.75 =666.67mg/l (ppm)
No of mole = 500/162 = 3.08 mmole
Morality concentration = 3.08/0.75 = 4.12 m mole/L
Normality concentration = 500/(81*0.75) = 8.24 N
666.67mg
L
81𝑔
𝑒𝑞𝑢𝑖𝑣𝑒𝑙𝑎𝑛𝑡
= 8.24𝑚𝑒𝑞𝑢𝑖
𝐿
Thus the concentration as CaCO3 = 8.24*50 = 412mg/l as CaCO3
Section III Water Chemistry
26
Example:
what mass of CO2 would be produced if (100g) of butane (C4H10) is completely
oxidized into CO2 and water?
2C4H10+ 13O2 8CO2 + 10H2O
Solution : from the balanced chemical equation
Each 2 mole of butan produces 8 mole of CO2
- Determine the number of mole of butane
No of mole = weight/MW = 100/58 = 1.724 molw
2 mole of CH4 8 mole of CO2
1.72 of CH4 X
Thus X= 1.72*8 / 2 = 6.8 mole of CO2 is produced
MW of CO2 = 44 g/mole
Thus the amount of CO2 is 6.8 * 44 = 303 g of CO2
Example: Commercial Sulphuric acid H2SO4 is often purchased as 93% solution. Find the
concentration (mg/l),the molarity and normality of the solution. If the specific gravity
of H2SO4 = 1.839.
Solution:
If H2SO4concentration is 100% , thus its itsspecific gravity will be 1.839
but since the concentration is only 93%
thus the solution S. gravity = 0.93* 1.839 = 1.710
MWH2SO4 = 2*1 + 1*32+4*16 = 98g/mole
Assume one litter of the solution:
Thus it contain 1710 g/l
Thus the molarity = 1710
𝑔
𝑙
98𝑔
𝑚𝑜𝑙𝑒
= 17.45𝑚𝑜𝑙𝑒
𝑙 𝑜𝑟 17.45 𝑀
Normality : MWH2SO4 = 98/2 = 48
N= 1710/48 = 34.9 eq/l
Section III Water Chemistry
27
Example: find the weight of sodium bicarbonate [NaHCO3] that is required to prepare 1M
solution?
MWNaHCO3= 84g/mole
1mole/l= mass
84𝑔/𝑚𝑜𝑙𝑒 = mass = 84g/l = 84,000mg/l
Section III Water Chemistry
28
Water
The source of water supply may be generally classified as
(a) Surface waters: (i) Rivers (ii) Lakes (iii) Impounding reservoirs
(b) Ground waters: (i) Springs (ii) Infiltration galleries (iii) wells.
GENERAL CHARACTERISTICS OF SURFACE WATERS:
1. More suspended impurities are present in surface waters.
2. Surface water may contain more pathogenic bacteria as pathogenic
bacteria are generally embodied in suspended impurities.
3. Surface water generally has color due to presence of Iron-oxide,
mineralogical compounds, suspended particles…. Etc
GENERAL CHARACTERISTICS OF GROUND WATERS:
1. Ground water contain large amount of the dissolved impurities.
2. It is generally free from suspended matter as it gets strained during its passage
through the porous underground strata.
3. It is soft or hard as it comes into contact with the Geological formations.
4. The Bacterial content is usually low due to the straining of suspended
impurities.
5. It may have taste and odour due to presence of organic matter dissolved during
passage through underground strata.
Water quality is studied for the following reasons:
1- Determine the degree of pollution
2- Determine the required step for W.T. P (water treatment plant)
3- Proper design for treatment unit
4- Check the effluent of WTP in reference with the specified standards.
Characteristic of water:
1- Physical characteristics
2- Chemical characteristics
3- Microbiological characteristics
4- Radiological characteristics
Section III Water Chemistry
29
Quality assessment of Harvested Rainwater for domestic use in Jordan
- The water samples were from Zarqa, Irbid, Jerash and Ajloun
- Water demand (available ) for Jordanian in 2008 is 160 m3/capita / year and is
expected to reach 90 m3/capita / year by 2025
Sources of Rainwater Harvesting In Jordan
1- Roof top of houses and institutions (schools, hospitals…etc)
2- Yard and garden
3- Street
Rainwater Harvesting In Jordan For
1- Drinking and domestic purposes (washing, bathing, cooking)
2- Irrigation and livestock
The Harvested Water Is Stored In:
1- Concrete tank : made from (bricks, reinforced concrete
Usually near the houses and collect the water from the roof
2- Rock tank with cement interior :
Usually in gardens and yards and collect the water street and yards
Quality of Harvested Rainwater depends on:
1- Location (in which governorate)
2- Catchment area
3- Public sewer system availability or use a septic tank
Effect of location on harvested rain water quality:
In Zarqa : the water was polluted by air pollution in the city that emitted from
chimneys (chemical pollutant such as iron (Fe),lead (pb), chromium (Cr), high
alkalinity and hardness)
Section III Water Chemistry
30
It was free from Chemical Oxygen Demand (COD) and Nitrate (NO3)
- For other governorate the main pollutants were Nitrate and biological
contaminants due to agricultural activities in Irbid, Ajloun and Jerash.
Effect of catchment area:
1- Roof top catchment:
-usually the main pollutants are from air and chimneys
-organic pollutant such as (COD, NO3, Ammonia) usually exist in yard and garden
catchment
2- Rock tank: since it collects the water from yard the main pollutants were
COD, Nitrate and biological
Effect of tank types:
1- Concrete tank: since it is included with houses , thus it collects the water from
the roof top.
2- Rock tank: it collects the water from yard thus it has same catchment area
effects.
Effect of public sewer availability:
- If public sewer is available: less biological contamination is expected
- If No public system : means dependant on septic tanks there is high risk of
biological contamination due to low maintenance and monitoring levels.
General conclusion: the harvested rainwater is suitable only for irrigation due
to effect of biological and pollutants contaminations.
Ammonia and nitrate (NO3) is sign for fertilizer and livestock pollution.
Section III Water Chemistry
31
A- Physical characteristics: it is associated with water appearance and includes
Parameter Range for Drinking Water (DW)
Temperature 15:20 oC
Turbidity ≤ 1 𝑁𝑇𝑈 (Nephlometric turbidity unit)
Color Colorless
Taste and Odor No odor
B- Chemical Characteristics:
- can be evident be their reaction like hardness , PH residual elements
- it includes also toxic substances such as organic matters, Nitrate (NO3),
Cyanides (CN) and heavy metals.
- It controlled by maximum allowable pollutants (organic, non-organic)
concentrations
Parameter Maximum Range for Drinking Water
(DW)
PH 6.5-8.5
Acidity
Alkalinity
Dissolved Oxygen
Hardness >300 mg/l
Chlorides >250 mg/l
sulphates 150-200 mg/l
Nitrates >45 mg/l
Iron 0.1 – 0.3 mg/l
Solids - Total dissolved Solid (TDS) >500*
- suspended solids
*if there is no other source it my increased to 1500 mg/l
C- Microbiological characteristics
- Mainly caused by microorganism activities like bacteria, Viruses, protozoa
- E-coli Fecal Coliform and total coliform tests are commonly used to
determine the water pollution with bacteria
- Their presence in water indicates pollution with human or animal fecal.
- Controlled by safe drinking water standards and wastewater effluent standard
- Usually the result presented by presence absence test, most probable
number (MPN)
Section III Water Chemistry
32
- For Filtered water Pseudomonas aeruginosa is tested , because it comes as a
result of unclean old filter.
D- Radiological characteristics
- The water should not contain any radioactive materials, that cause chronic or
cancer diseases
Solids: Types of impurities in water:
1- Suspended Solids (SS):
It is the large particle in water with diameter between (10-1
: 10-3
mm) such as
clay, salt, sand.
Note: ground water is usually free from SS? Why
-It cause the water turbidity
- Can be removed by filtration or sedimentation
-Turbidity measurement principle:
Section III Water Chemistry
33
2- Colloidal matters: its smaller particle size usually (10-3
: 10-6
mm) and can’t
be settled alone
- Can be removed by very high force centrifugation or using an additive
(coagulant)
3- Dissolved solids (D.S): it is the salts and dissolved organic matter
- Usually cause water problem like calcium and potassium carbonate and
bicarbonate
- Can be removed by distillation, adsorption , ion –exchange or liquid extraction
What is water conductivity? Ability of water to conduct
Electrical current
Max .value 5000 µS/cm
TDS [ppm] = 1.56 of
conductivity [µS/cm]
Why? Sugar and salt
Section III Water Chemistry
34
Exercise: At home: Bring a cup of water and dissolve the following:
1- One spoon salt (NaCl)
2- Single spoon of Sugar (C6 H12 O6)
3- Single spoon of very fine spice (any type)
4- Single spoon of fine sand
Describe to which W characteristic each one belong with justification?
SS Testing summary:
1- Dry known weight of water sample at 103 oC to 105
oC to drive off water in the
sample.
2- The residue is cooled, weighed, and dried again at 550oC to drive off volatile
solids in the sample.
3- The total, fixed, and volatile solids are determined by comparing the mass of the
sample before and after each drying step. Where
Laboratory procedure to determine TS and TVS Source: UMT
Total Suspended solid (SS) = ws
V
Volatile solid = 𝑤𝑠−𝑤𝑓
𝑉
Note: for water the each 1000ml= 1000g
Section III Water Chemistry
35
Example:
If the following data is obtained from a 100ml of water sample ,calculate TSS and
VS?
filter mass = 1.5413g
Mass after drying at 105 oC= 1.5541g
Mass after igniting at 550oC= 1.5519g
Solution:
Suspended solid (SS) (𝑤𝑠= 1.5541−1.5413
100/1000= 0.128 g/l = 128mg/l
Volatile solid = 𝑤𝑠−𝑤𝑓
𝑉 =
1.5541−1.5519
100/1000= 0.022 g/l = 22mg/l
Fixed solid (𝑤𝑓) = 1.5519−1.5413
100/1000= 0.106 g/l = 106mg/l
Dissolved Oxygen (DO):
- The source of D.O in water is photosynthesis and aeration
- It is one of important parameters to measure the water quality.
- It gives pleasure taste to water
- As the temp D.O
- If the D.O concentration decreases to less than 4mg/l all fish die
- If the D.O concentration is less than 2 mg/l all organism dies and the water is
called septic water
- Best D.O concentration is between 8-10 ppm. Optimum is 9ppm.
- The maximum naturally accrued is 14 mg/l.
Section III Water Chemistry
36
Biochemical Oxygen demand (BOD) :
- is the quantity of oxygen that is used by microorganism to stabilize the wastewater,
Usually measured after 5 days.
- a BOD test can be used to measure waste loadings to treatment plants, plant
efficiency and the effects of a discharge on a receiving stream, and to control the
plant process.
- It is indicator for the required aeration amount.
- The main equation describes the process is:
DO + organic matter CO2 + biological growth
- Drinking water usually has a BOD of less than 1 mg/L
- Ordinary domestic sewage may have a BOD of 200 mg/L.
-Any effluent to be discharged into natural bodies of water should have BOD less than
30 mg/L.
Test Summary:
1- The sample is filled in an airtight bottle and incubated at 20 oC for 5 days.
2- The dissolved oxygen (DO) content of the sample is determined before and
after five days of incubation at 20°C
3- and the BOD is calculated from the difference between initial and final DO.
The initial DO is determined shortly after the dilution is made; all oxygen uptake
Section III Water Chemistry
37
occurring after this measurement is included in the BOD measurement
Calculations:
BOD5 mg/l = (Initial DO - DO5) x Dilution Factor
Dilution Factor =Bottle Volume (300 ml)
𝑠𝑎𝑚𝑝𝑙𝑒 𝑉𝑜𝑙𝑢𝑚𝑒
BOD At any time:
BODt = L(1-10-kt
)…. Or BODt = L(1-exp-kt
)….
Where:
BODt : BOD at any time
L: ultimate bio-oxygen demand
k: oxygen decay constant, [day-1
]
t: time, [days]
However: The BOD reaction rate constant (K) is dependent on the following:
1. The nature of the waste:
- degradability of the organic matter. For example , Simple sugar
and starches are rapidly degraded
2. The ability of the organisms in the system to utilize the waste
Section III Water Chemistry
38
3. The temperature
- the water temperature may vary from place to place for the same river; hence, the
BOD rate constant is adjusted to the temperature of receiving water using
following relationship:
KT = K20 θ (T-20)
Where
T = temperature of interest, oC
KT = BOD rate constant at the temperature of interest, day-1
K20 = BOD rate constant determined at 20oC, day
-1
θ = temperature coefficient. This has a value of 1.056 in general and 1.047 for higher
temperature greater than 20oC
BOD incubator
Example:
Determine ultimate BOD for a wastewater having 5 day BOD at 20oC as 160 mg/L.
Assume reaction rate constant as 0.23 per day (base exp).
Solution
BOD5 = Lo ( 1 – exp-k.t
)
160 = Lo (1 – exp-5 x 0.23
)
Therefore, Lo = 234.1 mg/L
Section III Water Chemistry
39
Example:
A BOD test is done by pipiting 5 ml of waste water into 300 ml testing bottle. If the
initial DO was 8.4 mg/l and the DO after 5-days of incubation at 20 oC was 3.7mg/l,
calculate the BOD and estimate the 20-days BOD value assuming the reaction decay
constant k = 0.1 day-1
. (USE base 10)
Solution:
Dilution factor = 300/5 = 60
BOD5 = (8.4 – 3.7)*60 = 282 mg/l ….*
b- to determine the BOD after 20 days:
from (*) calculate L
282 = L (1-10−0.1 ×5 ) L = 412 mg/l
Thus BOD20 = 412 (1-10−0.1 ×20 ) BOD20 = 407.8 mg/l
Try the solution using Base (Exp ) but in this case the K = 0.23 day-1
Example:
The wastewater is being discharged into a river that has a temperature of 15oC. The BOD
rate constant determined in the laboratory for this mixed water is 0.12 per day. What
fraction of maximum oxygen consumption will occur in first four days? (Base Exp)
Solution
Determine the BOD rate constant at the river water temperature:
K15 = K20 (1.056) (T-20)
= 0.12 (1.056) (15-20)
= 0.091 per day .....
note 1: per day mean day-1...
note 2: as the temp decrease the reaction rate (K) decreases
Using this value of K to find the fraction of maximum oxygen consumption in four days:
BOD4 = Lo (1 – e-0.091x4
)
Therefore, BOD4 / Lo = 0.305
Section III Water Chemistry
40
Chemical oxygen demand (COD):
-Measure the amount of organic compounds in water that can be oxidized by strong
oxidant like mixture of sulfuric and chromic acids.
-Most applications of COD determine the amount of organic pollutants found in
surface water.
- It indicates of the strength (degree of pollution) of industrial WW that are not
biodegradable
- the test is faster than BOD test.
Section III Water Chemistry
41
Water PH
- Very important parameter that affects treatment processes, especially
coagulation, anddisinfection
- any unusual change may reflect a major event
H2O H+ + OH
-1 ,
A- kw = [H+] [OH
-1];;;; kw = 1 × 10−14
B- PH = -log[H+] [H
+] = 10
-PH
Where the [PH] is in Molar [mole/L]
Alkalinity :
- The source of alkalinity in natural water is bicarbonates that formed in reactions in
the soils through which the water percolates.
- It measures the capacity of water to neutralize acids (buffer capacity) in other
words its inherent resistance to pH change).
- river alkalinity values of up to 400 mg/l CaCO3
- it is determined by titration against standardized sulfuric acid (H2SO4)
- source of alkalinity is bicarbonate (main) carbonate and hydroxide
CO2 + H2O H2CO3 (carbonic acid)
H2CO3 H+ + HCO3
-1 Bicarbonate ka1 = 4.3 × 10−7
HCO3-1
H+ + CO3
-2 carbonate ka2 = 4.7 × 10−11
C- ka1 = 4.3 × 10−7 = [𝐻+] [𝐻𝐶𝑂3−1]
[H2CO3]
D- ka2 = 4.7 × 10−11 = [𝐻+] [𝐶𝑂3−2]
[𝐻𝐶𝑂3−1]
Alkalinity = [HCO3-1
]+2[CO3-2
] + [OH-1
] - [H+] …. Mole/l
-in a typical alkalinity problem , it is required to determine [H+]; [HCO3
-1]; [OH
-1];
[H2CO3]; [CO3-2
]
Section III Water Chemistry
42
Example:
a water has alkalinity of 250mg/l as CaCO3 and a PH equals 7.5, determine [H+];
[HCO3-1
]; [OH-1
]; [H2CO3]; [CO3-2
].
Solution:
1- PH = 7.5 = -log [H+] …
thus[H+] = 10−7.5 = 3.16 × 10−8 𝑚𝑜𝑙𝑒/𝑙
thus [H+] = 3.16 × 10−8 × 1 × 103 = 3.16 × 10−5 𝑚𝑔/𝑙
2- Kw = 10-14
= [H+][OH
-1] .. thus [OH
-1] =
10−14
3.16 × 10−8 = 3.16 × 10−7 𝑚𝑜𝑙𝑒/𝑙
[OH-1
] = 3.16 × 10−7 𝑚𝑜𝑙𝑒
𝑙 ×
17𝑔
𝑚𝑜𝑙𝑒= 5.37 × 10−6 𝑔
𝑙= 5.37 × 10−3 𝑚𝑔/𝑙
3- Determine the equivalent number of mole :
No of Eq. mole = weight/ eq. weight
250 × 10−3𝑔/𝑙
50𝑔/𝑒𝑞. 𝑚𝑜𝑙𝑒= 5 × 10−3 𝑚𝑒𝑞/𝑙
Thus
Section III Water Chemistry
43
CaCO3 Ca + CO3-2
- Every 1 mole of CaCO3 produces 1 mole of CO3-2
- 100g/mole of CaCO3 produces 60 g/ mole of CO3-2
- thus 250mg/mole of CaCO3 will produce = 250*60/100 = 150 mg of CO3-2
[CO3-2
] = 5 × 10−3 𝑒𝑞.𝑚𝑜𝑙𝑒
𝑙
Alkalinity = 5 × 10−3 𝑒𝑞.𝑚𝑜𝑙𝑒
𝑙= [HCO3
-1]+2[CO3
-2] + [OH
-1] - [H
+]…..A
ka1 = 4.3 × 10−7 = [𝐻+] [𝐻𝐶𝑂3−1]
[H2CO3]
ka2 = 4.7 × 10−11 = [𝐻+] [𝐶𝑂3−2]
[𝐻𝐶𝑂3−1]…. Thus
[𝐶𝑂3−2] = 4.7× 10−11
3.16× 10−7 𝑚𝑜𝑙𝑒/𝑙* [𝐻𝐶𝑂3−1] =1.48 × 10−4[𝐻𝐶𝑂3−1]
Substitute in A
5 × 10−3 𝑒𝑞.𝑚𝑜𝑙𝑒
𝑙= [HCO3
-1]+2×1.48 × 10−4]+[OH
-1] - [H
+]
[HCO3-1
]= 4.99× 10−3𝑞.𝑚𝑜𝑙𝑒
𝑙
Hardness:
- It is the capacity of a water to destroy the lather of soap.
- Causes economical losses.
- hardness mainly caused by the calcium (Ca+2
) and magnesium (Mg+2
)ions
- It is expressed as mg/l CaCO3
CaCO3 [mg/l] Type of water
Up to 50 ppm as CaCO3 Soft water
51- 100 ppm as CaCO3 Moderately soft
101-150 ppm as CaCO3 Slightly hard water
151-250 ppm as CaCO3 Moderately hard water
> 250 ppm as CaCO3 Hard water
There is a differences among countries in term of accepted water quality . in other
words, different water standards…..why?
Nitrate in Germany… blue baby …..
Section III Water Chemistry
44
Total Hardness: is the expression of the results of direct measurement (principally of calcium and
magnesium) expressed as mg/l CaCO3
Calcium Hardness: is the expression of the results of the measurement of calcium only, as mg/l CaCO3.
Magnesium Hardness:
is the difference between total hardness and calcium hardness is taken as the
magnesium hardness .
There are other types of hardness like Carbonate Hardness( is removed by heating)
, Non-carbonate Hardness and Permanent Hardness.
Ca+2
+ CO3 CaCO3
Mg+2
+ OH- Mg[OH]2
Molecular weight of CaCO3 = 1*40 + 12 + 3*16 = 100 g/mole
Equivalent weight = Mw/charge = 100/2 = 50 g/eq. weight
Example:
the result of water analysis show the following for cations :calcium 35.8; magnesium
9.9; sodium 4.6 and potassium 3.9 ppm. While the anions were chloride 7.1; HCO3-1
131; SO4-2
26.4, draw a milliequivalent – per litter bar graph and express alkalinity
and hardness in unit of mg/l as CaCO3?
element Conc. [mg/l] Equ. weight M eq/l
Major cations Ca+2
35.8 20 1.79 Mg
+2 9.9 12.2 0.81
Na+ 4.6 23 0.20
K+ 3.9 39.1 0.10
Total cation 2.9
Major anions HCO3-1
131 61 2.15 SO4
-2 26.4 48 0.55
Cl-
7.1 35.5 0.20 Total anion 2.9
Note: usually total anions equal total cations; remember the arrangement
Thus we have:
1.79 meq/l of Ca(HCO3)2
0.36 meq/l of Mg(HCO3)2
0.45 meq/l of MgSO4
Draw milieq./l bar
graph
Section III Water Chemistry
45
0.1 meq/l of KCl
0.1 meq/l of Na2 SO4
0.1 meq/l of NaCl
thus total carbonate hardness = 1.79 +0.36 = 2.15 meq/l
2.15 meq/l * 50 mg/meq = 107.5 mg/l as CaCO3
- total non-carbonate hardness
= 0.45 * 50 = 22.5 mg/l as CaCO3
Example 2:
element Conc. [mg/l] Equ. weight m eq/l
Major cations Ca+2
29 20 1.45 Mg
+2 16.4 12.2 1.34
Na+ 23 23 1.00
K+ 17.5 39.1 0.45
Total cation 4.24
Major anions HCO3-1
171 61 2.81 SO4
-2 36 48 0.75
Cl-
24 35.5 0.68 Total anion 4.24
1.45meq/l of Ca(HCO3)2
1.34meq/l of Mg(HCO3)2
0.02 meq/l of Na(HCO3)
0.75meq/l of Na2 SO4
0.23 meq/l of NaCl
0.45 meq/l of KCl
Total hardness = 1.45 + 1.34 = 2.79
2.79* 50 = 139.5mg/l as CaCO3
Hardness is determined (tested) in Lab by tetrametric with EDTA
1.79 Ca++ 0.81 Mg++ 0.2 Na+ 0.1 K+
2.15 HCO3- 0.55SO4
-2 0.2 Cl
-
Section III Water Chemistry
46
Residual Chlorine :
Section III Water Chemistry
47
Heavy Metals:
Volatile Organic Matter (VOC):
- Emitted mainly from chemical and petrochemical industries, which include
most solvents such as thinner cleaners,lubricants, and liquid fuels.
- The most commonly reported VOC’c are:
1- formaldehyde (CH2O),
2- tetrachloroethylene (C2Cl4),
3- benzene (C6H6),
4- toluene (C7H8),
5- xylene (C8H10)
6- and acetaldehyde (C2H4O).
- VOC’s are hazardous to environment because they severely affect
- both human health and environment such as global warming;
- destroy the ozone layer
- and photochemical smog [1-3].
- Especially, benzene and toluene are known to cause cancer in animals.
- Technologies used to control VOCs can be subdivided into two major sections:
I) Decomposition:
This method involves thermal oxidation and/or bio-filtration methods to reduce
the effects of emissions by decomposing VOCs.
Section III Water Chemistry
48
II) Recovery: Absorption, adsorption, and condensation are common recovery
technologies.
various technologies for VOC removal have been investigated in recent years, with
treatments now including:
1- thermal oxidation,
2- bio-filtration,
3- absorption,
4- adsorption,
5- and condensation
Extra Examples:
Example 1:
A water treatment plant produces 100kg of dry weight of sludge daily, this sludge is
removed with 10m3
of water. What is the percentage solid concentration in the
effluent? And what is the ppm concentration assuming the water density is
1000kg/m3?
Sludge % concentration= 100 kg dry sludge
100 𝑘𝑔 𝑠𝑙𝑢𝑑𝑔𝑒+10,000 𝑘𝑔 𝑤𝑎𝑡𝑒𝑟 × 100% = 0.99%
Sludge concentration (ppm) = 100 kg dry sludge×106
10,000 𝐿𝑖𝑡𝑒𝑟 𝑜𝑓 𝑤𝑎𝑡𝑒𝑟 = 10,000 ppm
Example 2:
Commercial sulfuric acid (H2SO4) is often produced as 93% W/V? find the
concentration of H2SO4 [ ppm], and the molarity and normality of the solution. If the
specific gravity of H2SO4 is 1.839
Solution:
Since the S.G = 1.839 then
1L of H2SO4 = 1.839 kg /L= 1839g/L
Section III Water Chemistry
49
But each litter contains only 93% of H2SO4
then H2SO4 in 1L = 0.93 * 1839g/L = 1,710g/L = 1.710 * 106
ppm (mg/L) #1
#2:
MWH2SO4 = 98g/mole
Then the molarity = 1,710g/L
98g/mole = 17.45 mole/L or 17.45 M
#3 the Normality
Equiv Weight of H2SO4 = 98/2 = 48g/equiv
Then the normality = 1,710g/L
48g/equiv = 34.9 equiv./L or N
Example3
If the solubility constant of AlPO4 dissolution in water is (Ks) = 10-20
what is the
concentration of such solution that is in equilibrium with water?
AlPO4Al+3
+ PO4-3
for every mole of AlPO4 produces one mole ofAl+3
and one mople of PO4 -3
(Ks) = 10-20
= [Al+3
] [PO4 -3
]
10-20
= X2
…. Then X = [PO4 -3
] = 10-10
mole/l
Since MWPO4 -3 = 95g/mole
Thus the final [PO4 -3
] in mg/l = 95g/mole * 10-10
mole/l = 9.5 * 10-6
mg/l
Example4:
If 100 mg of H2SO4is added to1L of water what is the final PH?
Solution
Section III Water Chemistry
50
[H2SO4] = 100mg/L
98 g/mole×
1𝑔
1000 𝑚𝑔 = 1.02 ×10
-3mole/L
The reaction is:
H2SO4 2H+
+ SO4 -2
Every mole of H2SO4 produces 2 mole of H+
then 1.02 ×10-3
mole/L needs = 2* 1.02*10-3
= 2.04*10-3
mole of H+
PH = -log [H+] = 2.69
Section IV Water Treatment - Introduction
51
The main purpose of water treatment is:
- To protect both human and environmental health,
- To save water by using the treated
- To protect the ground water resources form pollution.
Water source could be
River
Lakes and moorland (swamp)
Groundwater; most likely better quality than surface water
Rainwater ++/ Dam
Raw water quality varies with the source, and if the source is surface water,
the quality vary seasonally, particularly with flooding, upland and lowland, etc
Section IV Water Treatment - Introduction
52
Sources of Water pollution:
Section IV Water Treatment - Introduction
53
Section V Water Treatment Plant-conventional Treatment
54
Conventional water treatment:
is a combination of coagulation-Flocculation, sedimentation, filtration and
disinfection process.
1- Primary treatment involves : pumping, screening and grit removal
- Screening: aims to remove large objects, such as stones or sticks, that could
plug lines or block tank inlets.
- grit chamber- slows down the flow to allow grit to fall out
- sedimentation tank (settling tank or clarifier): settleable solids settle out and
are pumped away, while oils float to the top and are skimmed off
The typical functions of each unit operations are given in the following table:
Functions of Water Treatment Units Unit treatment
Function (removal)
Aeration, chemicals use Colour, Odour, Taste
Screening Floating matter
Chemical methods Iron, Manganese, etc.
Softening Hardness
Sedimentation Suspended matter
Coagulation Suspended matter, a part of colloidal matter and bacteria
Filtration Remaining colloidal dissolved matter, bacteria
Disinfection Pathogenic bacteria, Organic matter and Reducing
Section V Water Treatment Plant-conventional Treatment
55
Aeration:
- It removes odor, color and taste due to reducing the concentration of volatile
gasses like H2S (hydrogen sulfide) , and algae and other related organisms.
- It oxidizes iron and manganese,
- increasing [DO], removes CO2 , CH4 and other flammable gasses, reduces
corrosion.
- Its work principle is based on the fact that the atmospheric oxygen will replace
the volatile gasses in water , while it will escape into atmosphere.
- The replacement will continue till reaching the equilibrium depending on the
partial pressure of each specific gasses.
Type of aeration:
1- Gravity aerators:
In this type water is allowed to fall by gravity, such that large area of water will
exposed to atmosphere.
2- Fountain (Spray) aerators
A special nozzle is used to produce a fine spray. Each nozzle is 2.5- 4cm diameter.
Discharging about 18-36 L/h
Nozzle spacing should be such that each meter cube of water (m3) has aerator area of
0.03 – 0.09 m2 for one hour.
3- Injection or Diffused aerator :
- It consists of tank with perforated pipes, tube or diffuser plates, fixed at the
bottom to release fine air bubbles from compressor unit.
- The tank depth is 3-4m and the tank width is 1.5 times of tank depth.
- If the depth is more the diffusers must be placed at 3-4m below the water
surface
Section V Water Treatment Plant-conventional Treatment
56
- Aeration time is 10-30 min and 0.2-0.4 litter of air is required per litter of
water.
- Increase the diffuser depth increases the aeration rate and efficiency
- Decrease the orifice size increases the aeration rate and efficiency
4- Mechanical aerator:
Mixing paddle as in flocculation are used.
Section V Water Treatment Plant-conventional Treatment
57
The puddle may be submerged or at surface.
Section VII Water Treatment - Coagulation
58
Settling (Sedimentation)
it is a type of solid liquid separation process in which a suspension is separated into two phases:
a- Clarified supernatant leaving the top of the sedimentation tank (overflow).
b- Concentrated sludge leaving the bottom of the sedimentation tank (underflow).
Purpose of Settling
To remove coarse dispersed phase. To remove coagulated and flocculated impurities.
To remove precipitated impurities after chemical treatment. To settle the sludge (biomass) after activated sludge process /
tricking filters.
Principle of Settling
Suspended solids present in water having specific gravity
greater than that of water (1) tend to settle down by gravity as soon as the turbulence is retarded by offering storage.
Basin in which the flow is retarded is called settling tank. Theoretical average time for which the water is detained in
the settling tank is called the detention period. Sedimentation tanks are circular or rectangular.
Sedimentation types:
It exist, based on characteristics of particles. 1- Discrete or type 1 settling particles whose size, shape, and specific gravity do not
change over time (has a density (ρ) = 2000 – 2200 kg/m3).
2- Flocculating particles or type 2 settling; particles that change size, shape and
perhaps specific gravity over time(has a density (ρ) = 1030 – 1070 kg/m3).
3- Hindered settling or type 3 settling: blanket sedimentation occurs at Lime
softening sedimentation and Sludge thickeners in water treatment
4- Compressed settling or type 4 settling occurs Sludge thickeners in water treatment
Section VII Water Treatment - Coagulation
59
Applications in Water Treatment:
1. grit removal
2. suspended solids removal in primary clarifier
Place of Sedimentation in various WW plant:
Or
Section VII Water Treatment - Coagulation
60
For treating hard water to removes flocculated solids. The sedimentation tank comes after the flocculation tank.
Section VII Water Treatment - Coagulation
61
Section VII Water Treatment - Coagulation
62
Section VII Water Treatment - Coagulation
63
Section VII Water Treatment - Coagulation
64
Sedimentation process:
It is a physical treatment that allows for particles having specific gravity higher than
water to settle under its own weight.
Factor affecting the sedimentation:
1- Water prosperities:
a) Sed. Decreases when water viscosity increase
b) Sed. Decreases when water density increase
c) Sed. Increase when water temp. Increase.
2- Suspended solids concentration, size and shape
3- Detention time: sed. Efficiency increase by increasing the water retention at
the tank , but after time the precipitation is decreased sharply thus the time
should be determined correctly. (2-4hr)
4- Flow velocity: decrease the flow velocity increase the sed. The max.
Allowable velocity in the tank is 0.3 m/sec
5- Tank shape: circular tanks are more efficient for sedimentation
Ideal sedimentation tank:
1- The flow is laminar
2- There are no dead zones
3- The horizontal velocity is constant
4- Good arrangement of inlet and outlet weirs.
Type of sedimentation:
1- Plain sedimentation: no chemical is used
2- Chemical sedimentation: chemical is used to enhance the efficiency
Critical Settling Velocity & settling Velocity (Overflow rate)
- Settling velocity Vs or as called overflow rate
Section VII Water Treatment - Coagulation
65
Particles move horizontally with the fluid (all particles have the same horizontal
velocity)
Particles move vertically with terminal settling velocity(different for particles
with different size, shape and density)
All particle with Vs,o>Vcwill be completely settled.
All particle with Vs,o<Vcwill be removed in the ratio Vp/Vc
Section VII Water Treatment - Coagulation
66
Available length = Circumference
of Circleمحيط الدائرة
Section VII Water Treatment - Coagulation
67
In plain sedimentation : no chemical is used the precipitation just is done by gravity
Example:
Design the plain rectangular sedimentation tank for a water purification of an hourly
output 5000m3 if the retention time is 4hr, then get the amount if the sludge in the S.S
if the raw wastewater has SS concentration 80ppm and the sludge specific gravity is
1.1?
Solution:
Assume Surface .Load .Rate (S.L.R) = 30 m3/m
2/day
Thus the minimum total volume = 4 * 5000 = 20,000 m3 = n.w.l.d
Thus total tank area = 5000 * 24 / 30 = 4000 m2
=No. of tank * length* width of tank
4000m2 = n.l.w
Then the water depth = 20,000/ 4,000 = 5m.
Assume number of tank = 8 then each tank area = 500 m2
then the tank width = =√500
4 = 11.2 make the width = 10m
then the length = 50m ,
Section VII Water Treatment - Coagulation
68
then each tank volume = 10*50*5 = 2,500 m3
actual total volume = 2,500 * 8 = 20,000 m3
Check:
Actual Retention time = 20,000/5000 = 4hr .ok
Actual SLR = (5000/4000)*24 = 30 m3/m
2/d . ok
Hydraulic .Line (H.L) = 5000 ×24
8 ×50 = 300 m3
/m/d .ok
Sludge Amount:
S.S = 80 mg/l ; assume Recovery .Rate (R.R) = 80%
Then the amount of sludge per day = Y 9ton/day)
= 5000 × 24 (m3/d)
×80 ×0.8
106 = 7.68 ton/day
Assume the S.S concentration in the sludge = 3%
Thus the total amount of sludge (water + SS) = 7.68/0.03 = 256 ton/day
Thus the total sludge volume = 256/1.1 = 232 m3/day
Section VII Water Treatment - Coagulation
69
Coagulation Flocculent Sedimentation ( type 2 and 3):
- The design procedure for sedimentation tanks of type 2 and 3 are
the same as type 1.
- The difference is mainly in the overflow rate (vs)???
- The following table gives the design criteria of these two types.
Typical sedimentation tanks design dimensions :
A- Rectangular Tank
- depth: 3-5 m
- length: 15-90 m
- width: 3-24 m
B- Circular Tank
- depth: 3-5 m
- diameter: 4-60 m
C- Retention time 2-4 hr
D- Tank bottom slope 1-2%in rectangular tank; 2-4% in circular tank
E- The weir (الهدارات) length should be 1/7 of total tank length
F- Surface load rate = Q/ (total surface area)= 𝑄
𝑛.𝐴= over flow rate = 20-40m
3/m
2/d
Where n = number of tanks
G- Hydraulic load (H.L) on outlet weir = weir loading rate = over load =
H.L =𝑄/(𝑛. 𝐿𝑤) = 150 − 300 m3/𝑚/𝑑
H- Horizontal velocity ≤ 0.3 𝑚/𝑚𝑖𝑛
sizes change shape change specific gravity change
Section VII Water Treatment - Coagulation
70
Example:
a circular clarifier (sedimentation tank) will be used to treat 3000m3hourly, assume
the surface area of the tank is 2400 m2
estimate the tank dimensions?
Solution :
Water depth =
Assume tank diameter = 30m thus number of tank =
No of tank = n× 𝜋 × 302
4= 2400
Thus n = 3.4 take 3 tanks
Modify the required diameter :
3× 𝜋 × 𝑑
2
4= 2400 d = 32m
S.L.R (over flow) = 3000×24
3×𝜋 × 322
4
= 29.8 m3/m
2/d within the range (20:40)
H.L= Q/Lw = 3000×24
3×𝜋 ×32 = 238 m
3/m/d within the range (150:300) .OK
Section VII Water Treatment - Coagulation
71
Coagulation :
Particles smaller than 10 µm are difficult to remove by simple settling or by filtration.
It is a chemical addition process of coagulant, it consists two steps
Source: Terry L. Engelhardt, HACH
5- Coagulation is a process to neutralize the particles charges
6- form a gelatinous mass (floc) to trap (or bridge) particles thus forming a mass large
enough to settle or be trapped in the filter
Aims of Coagulation:
7- Reduce retention time
8- Increase filtration rate
Section VII Water Treatment - Coagulation
72
9- Improve water quality
10- Increase sedimentation efficiency (90 – 96%)
Coagulation used chemicals:
A- Alum (Aluminiumsulphate )
B- Iron based salts
1- Ferric Sulfate (Fe2SO
4 · 9 H2O )
2- Ferric chloride (FeCl
3)
C- Sodium Aluminate, NaAlO2
D- Polyelectrolytes or resin: is generally low molecular weight (<500,000) it may be
anionic or cationic
Factors affecting coagulation:
1- Water PH
2- Water temperature
3- Coagulant doase
4- Coagulant type
5- Mixing type
Coagulation process:
1- Coagulant addition: wet or dry
2- Mixing
3- Flocculation,
4- Sedimentation
Coagulant feeding:
a- Dry feeding:
- the coagulant is added as powder to the water
- Main limitations are: hard to control the optimum doase, more workers and the
powder is sensitive to humidity.
b- Wet feeding:
- a solution from the coagulant is prepared in a separate tank
- High dispersion rate, and easy to control
- The solution is prepared by rabid mix (flash) mix
Section VII Water Treatment - Coagulation
73
The Jar Test is used to determine the optimum Dose
1- it is the most basic test for control of coagulation/flocculation/filtration
How to determine the optimum coagulant and dosage using the jar test:
1- do the basic analysis for water (PH, Alkalinity, Hardness, Temp)
2- in each jar add different coagulant (choose the doase between 20:30mg/l)
3- flash mix for 30 sec (100:300rpm)
4- gentle mix for 10 min (20:30 rpm)
5- allow for sedimentation (30:40 min)
6- get removal efficiency for each vessel (depth of sedimentation solids)
7- determine the best coagulant
8- repeat the steps from 2-7 using the best coagulant in step (2) add different
dosage (10:60 ppm) now determine the optimum doase
Note: optimum PH is determined by repeating the steps 2-7.
Design of mixing tank:
Tank volume = 𝑸×.𝑺
𝑪×𝜸×.𝒏×.𝟏𝟎𝟔
where
Section VII Water Treatment - Coagulation
74
S:coagulant dose
C: Coagulant concentration
𝜸: solution spesific gravity usually (1.02 − 1.07)
n: number of tanks
usually the tank is circular with dimensions is
d= 1:2m
n≥ 2
Example: Jar test
two sets of jar test on raw water with turbidity = 15TUand an HCO3- concentration =
50ppm expressed as CaCO3, given the below data find the optimum PH, coagulant
dose, and the theoretical amount of alkalinity that can be consumed at the optimal
dose?
First test:
1 2 3 4 5 6
PH 5 5.5 6 6.5 7 7.5
Alum dose (ppm) 10 10 10 10 10 10
Turbidity (TU) 11 7 5.5 5.7 8 13
Second test:
1 2 3 4 5 6
PH 6 6 6 6 6 6
Alum dose (ppm) 5 7 10 12 15 20
Turbidity (TU) 14 9.5 5 4.5 6 13
Thus from the result the optimum PH is 6.25 and the optimum doase = 12.5mg/l
Al2(SO
4)3 · 14 H
2O + 6HCO
3
-1 2Al(OH)3
+ 3SO4+ 6CO2
+ 11H2O
From the equation:
1 mole alum 6 mole HCO3
-1
Section VII Water Treatment - Coagulation
75
thus
594 g/mole 6*61 g/mole
12.5 of alum X g/mole of carbonic acid
X = carbonic acid mass consumed = 12.5 ×6×61×10−3
594𝑔/𝑚𝑜𝑙𝑒= 7.7 × 10−3 𝑔/𝑙 = 7.7 mg/l
To represent the consumed mass by CaCO3
7.7 ×50
61= 6.31 mg/l as CaCO3
Coagulant Mixing:
This strep aims to disperse the coagulant solution in the sedimentation tank
Type of mixing:
1- coagulant injection to suction pipes of Low .Lifting .Pump
2- hydraulic mixing :
- using hydraulic weirs that causes water jump or using the venturi pipe
- low coast and easy to operate and maintain
3- Mechanical Mixing:
- Using a mixer with 150:200 r.p.m
Section VII Water Treatment - Coagulation
76
Mechanical mixing
Design of mixing tank: it can be square or circular
Retention time = 5:60 sec
D= 2:4m
n≥ 1
Section VII Water Treatment - Coagulation
77
Velocity Gradient calculation:
It is used to measure the degree of mixing
G= √𝑷
µ×𝑽
G: velocity gradient = velocity/distance [sec-1
] usually 300:500sec-1
P: motor power in watt
µ: 𝑤𝑎𝑡𝑒𝑟𝑣𝑒𝑠𝑐𝑜𝑠𝑖𝑡𝑦 (N.sec/m2) depends on water temp. (1.014 𝑋 10
-3)
V: mixing tank volume
B-Flocculation or gentle mixing tank:
-It is used to complete the reaction and interaction between the SS and the coagulant
solution ,
-The SS aggumulerate to form a flocks(increase the size and the weight)
Type of Flocculation tanks:
1- Hydraulic type: it is a tank with vertical or horizontal
Maze Flocculation basin , source (google image)
2- Mechanical mixing: it uses paddle to mix the water
Section VII Water Treatment - Coagulation
78
Flocculation tank design
Time retention = 20: 30 min
D = 2:4m
L = 3:5m
n≥ 2
Example:
If Q =60000m3
daily, and the required alum dose = 40ppm calculate the
1- The required Alum solution tank and alum doase (dosage) if the alum
concentration in thank is 10%
2- The volume of flash mixing tank, if retention time is 30sec
3- The dimension of rectangular flocculation tank (L=3b)if retention time is
20min
Solution:
Total required volume = 𝑸×.𝑺
𝑪×𝜸×.𝒏×.𝟏𝟎𝟔
= 𝟔𝟎,𝟎𝟎𝟎 𝒎×𝟒𝟎
𝟎.𝟏×𝟏.𝟎𝟏×.𝟏𝟎𝟔= 24m3
assume 3 tanks then each tank has a volume of 8m3
assume water depth d= 2 then
tank area = 8/2 = 4m2
thus the tank is square length = 2m , n = 3, and water depth = 2
step by step solution:
daily alum dose required = 60000 * 40 * 10-6
= 2.4 ton/day of alum
but alum concentration = 0.1 then the required mass = 2.4/0.1 = 24 tons
the required volume = mass/density ... assume the solution density = 1ton/1.01ton/m3
thus the required volume = 24m3
Section VII Water Treatment - Coagulation
79
Rate of dosing:
Dosing rate = required alum volume / time
24m3
/day 1000
24 ×60 = 16.67l/min
2-For flash mixing tank:
Q = 60000 𝑚3
𝑑𝑎𝑦 =
60000
24 ×60 = 41.67 m
3/min
V= Q * retention time = 41.67 * 30/60 = 20.835 m3
If the tank is circular (one tank)
V = π/4 * φ2
* d ... assume φ= d
Then d= 3m and tank diameter = 3m
3-for flocculation tank
V = 41.67 m3/min * 20 min = 833.4 m
3
Assume two tanks and water depth in each tank = 3m
Required area of each tank = 833.4 / (2*3) = 139 m2
thus b = 6.8m and l = 20.4 m
thus the final design: 2 tanks of l=20.4m and b=6.8m and water depth 3m
Section VII Water Treatment - Coagulation
80
Development of coagulation-flocculation and sedimentation system:
A- At the first each process was done in separated tank as the following picture
B- Improvement was done to use one tank for flocculation part and sedimentation
part
Section VII Water Treatment - Coagulation
81
C- One circular tank is used and called clariflocculater
It is very efficient , the SS removing efficiency may reach 96%
Retention time in the inner tank is 20:30 min...for flocculation
Retention time in the outer tank 2:3hr..... for sedimentation
Section VII Water Treatment - Coagulation
82
Clariflucculator basic design :
For outer part:
To = 2:3 hr (total time for flocculation and sedimentation)
do = 3:5m
φo≤ 35𝑚
For inner part:
Ti = 20:30min
di = do - (0.5:1m)
ni = no
φi= (0.3: 0.5 )𝜑𝑜
Check:
Lw
Surface Load Rate (S.L.R) = 𝑄
𝑆𝑢𝑟𝑓𝑎𝑐𝑒 𝑎𝑟𝑒𝑎 =
𝑄
𝑛.𝜋
4 .(𝜑𝑜
2−φi2) = 25:40m
3/m
2/day
Section VII Water Treatment - Coagulation
83
Hydraulic Load Rate (H.L.R) = 𝑄
𝑤𝑒𝑖𝑟 𝑙𝑒𝑛𝑔𝑡ℎ (𝑙𝑤 ) =
𝑄
𝑛.𝜋 .(𝜑𝑜)
≤ 300m3/m/day
Note: if mention retention time in sed. Tank = 2.5hr
And retention time in floc. Tank =30min
Thus the To = 2.5+0.5 = 3hr
Ti = 0.5hr
Treated water by coagulation can be measured by:
1- Zeta potential
2- Streaming Current : it is an on-line measurement of how well charge
neutralization has occurred
Example:
Design clarifluccolator tanks for water treatment plant of a daily flow (Q) = 48000m3
And working hours is 16hrs per day?
Solution:
Q = 48000 𝑚3 /𝑑𝑎𝑦
16ℎ𝑟/𝑑𝑎𝑦 = 3000m
3/hr
Outer tank design:
Retention time To = 3hr +0.5 = 3.5hr
Thus the required volume = 3000 *3.5 = 10,500 m3
assume water depth in the tank (d) = 3m
thus the required total surface area = 10,500m3/3m = 3500m
2
total area=3500 m2
= n ×𝜋
4× 𝜑𝑜
2assume 𝜑𝑜 = 35m
thus n = 3.6 use 4 tanks
thus𝜑𝑜 = 33.4𝑚
Section VII Water Treatment - Coagulation
84
Design of inner tank:
Ti = 0.5hr
Required volume = 3000 * 0.5 = 1500m3
Di = d0 – (0.5:1m) = 3 -0.75 = 2.25m
Thus the required surface area = 1500/2.25 = 666.67m2
use 4 tanks ...
666.67 m2
= 4 ×𝜋
4× 𝜑𝑖
2
thus the required 𝜑𝑖 = 14.6m
Check:
S.L.R = 𝑄
𝑠𝑢𝑟𝑓𝑎𝑐𝑒 𝑎𝑟𝑒𝑎=
3000𝑚3
ℎ𝑟×24ℎ𝑟
𝑛.𝜋4
.(33.42
−14.62
) = 25.4m
3/m
2/day
H.L.R = 𝑄
𝑤𝑒𝑖𝑟 𝑙𝑒𝑛𝑔𝑡ℎ (𝑙𝑤 ) =
3000∗24
𝑛.𝜋 .(33.4) 171.5 m3
/m/day
Vh =
𝑄
𝑐𝑟𝑜𝑠𝑠 𝑠𝑒𝑐𝑡𝑖𝑜𝑛𝑎𝑙 𝑎𝑟𝑒𝑎 =
3000/60
𝑛.𝜋 .(14.6)∗3 = 0.09 m/min
φi= (0.3: 0.5 )𝜑𝑜 𝑡ℎ𝑢𝑠
φi
𝜑𝑜 =
14.6
33.4 = 0.44
Example:
For an existing water treatment plant with 4 clarifluculator with the following
dimension find the Max population that can be served
φo= 32m φi = 14m
do = 3.5m di= 3m
if Wc = 300L/c/day and water pump = 20hr
Solution:
- In such question the answer dose not consider the tank volume only but the
discharge from each tank (SLR;HLR, and Vh) then we determine the minimum
Section VII Water Treatment - Coagulation
85
discharge which is equal to the maximum allowable discharge for the
treatment plant.
For outer part:
Tank volume or capacity = Q.T
To find the total retention time we estimate the sedimentation time (2hr) and the
flocculation time (20min) … thus T = 2.33 hr (which allow for max Q)
Q = 4×
𝜋
4 ×322 ×3.5
2.33= 4832 m3
/hr
From S.L.R
S.L.R = 𝑄 𝑝𝑒𝑟 𝑑𝑎𝑦
𝑠𝑢𝑟𝑓𝑎𝑐𝑒 𝑎𝑟𝑒𝑎 = 25: 40 …take 40 to get the max. flow
Then Q2 = (40/24) × 4 ×𝜋
4 × (322 − 142 ) = 4335.4 m
3/hr
-note: S.L.R is converted to hr by dividing on 24 but not 20 (pump regime)
From H.L.R
H.L.R = 𝑄 𝑝𝑒𝑟 𝑑𝑎𝑦
𝑛.𝑙 𝑤𝑒𝑖𝑟= 300 m3
/m/day
Thus Q3 = (300/24) × 4 × 𝜋 × 32 = 5026.5 m3/hr
From Vh
Vh = 𝑄
𝑋.𝐴 = 0.3 m/min
Q4 = (0.3 *60) × ( 4 × 𝜋 × 14) × 3.5 = 11,875 m3/hr
- X.A is perimeter (circumference )of cylinder at the face of the internal tank
multiplied by water depth in the outer tank.
For inner part:
c = T.Q
from capacity: T = 0.33 hr
Q5 = 4×
𝜋
4 ×142 ×3
0.33= 5597.7 m
3/hr
-So maximum hourly flow from the plant is the minimum Q value =4335.4 m3/hr
Section VII Water Treatment - Coagulation
86
- Maximum daily flow = 4335.4 m3/hr * 20 hr = 86,708 m
3/day
Thus maximum served population can be =𝑄𝑑𝑎𝑖𝑙𝑦
𝑊𝑐
= 86,708 m3/day
0.3𝑚3
𝑐/𝑑𝑎𝑦
= 289,027 capita
Section VIII
87
Water intake:
- Aims to safely withdrawing water from the source
- Its location is predetermined under specific pool levels
Factors Governing Location of Intake:
- The site should be near the treatment plant so that the cost of conveying water
is less.
- The intake must be located in the purer zone of the source to draw best quality
water from the source, thereby reducing load on the treatment plant.
- The intake must never be located at the downstream or in the vicinity of the
point of disposal of wastewater.
- The intake must be located at a place from where it can draw water even
during the driest period of the year.
- The intake site should remain easily accessible during floods and should not
get flooded.
Types of water intake:
1- Pipe intake:
- It is best type, good water quality
- Used when water level is changing
- Used for long distance water transmission
Section VIII
88
2- Shore intake:
-The water intake is placed directly near the water source like river bank
-The pumped waster quality is low due to pollution risk
-Good for industrial and agricultural water uses
-Low discharge capacity
Section VIII
89
3- Submerged (deep) intake:
- Used in narrow and deep water streams
- when the water cover is polluted
- When the water stream is used for sailing
Section VIII
90
4- Tower intake:
- Used for large water surfaces (lakes , dams)
- When water level is varied
- Water quality is varied with water depth
Water intake design depend mainly on water consumption
Section VIII
91
Filtration
- The resultant water after sedimentation will not be pure, and may contain
some very fine suspended particles and bacteria in it.
- To remove or to reduce the
a- remaining impurities
b- Algae
c- Iron and manganese salts
d- Color and taste of water
- The water is filtered through the beds of fine granular material, such as sand,
etc.
Filtration rates for granular media filtration are typically expressed at the number of
gallons filtered per square foot of filter surface area per min, gal/ft2/min or m3/m
2/hr
It is called filtration rate or Flux
Filter Materials
1- Gravel:
- It supports the sand layer, uniformly distribute the effluents
- It permits the filtered water to move freely to the under drains, and allows the
wash (backwash) water to move uniformly upwards.
Section VIII
92
2- Sand:
It is either fine or coarse, is generally used as filter media.
- The size of the sand is measured and expressed by the term called effective size.
The effective size, i.e. D10 may be defined as the size of the sieve in mm through
which ten percent of the sample of sand by weight will pass.
- The uniformity in size or degree of variations in sizes is represented by uniformity
coefficient. The uniformity coefficient, i.e. (D60/D10)
3- Other materials:
Such as Anthracite that is made from anthracite, which is a type of coal-stone that
burns without smoke or flames.
It is cheaper and has been able to give a high rate of filtration, remove odor .
Section VIII
93
Types of Filter:
Slow sand filter: (SSF)
- it consists of fine sand, supported by gravel.
- it captures particles near the surface of the bed and are usually cleaned by
scraping away the top layer of sand that contains the particles.
- The filtration is done on the layer (sticky, gelatinous film)
- The layer takes several weeks to form can consist of bacteria, fungi, protozoa,
alga, and microscopic aquatic organisms, once fully
- water turbidity should less than <50 NTU
- filtration rate = 0.05 gal/ft2/min
Section VIII
94
Construction of SSF
a- 1.2 : 1.5 m of water depth at the top
b- 0.9 : 1.5 m layers of fine sand with effective size (D10 = 0.25:0.35mm) and
uniformity coefficient (Cu = 1.75)
c- 0.3:0.6 m of well graded Gravel
d- Under-drainage system : which is group of pipes that collect the filtered water
into main pip
SSF operation and maintenance:
1- Prepare the filter layers (gravel, sand) then fill with water for 2-3 weeks to
form the dirty skin (stick layer)
2- The produced water during the preparation period is not usable.
3- Pass the water to be filtered for a period of 2-5 months ,
4- When significant the pressure drop is happened. Stop water inlet and clean the
filter
5- Filter cleaning: by removing the top sand and stick layers and replace the sand
Section VIII
95
Design Data:
Rate of Filtration (R.O.F) = 5:8 m3/m
2/day
No of tank ≥ 2 𝑤𝑜𝑟𝑘𝑖𝑛𝑔 + 𝑛𝑐𝑙𝑒𝑎𝑛𝑖𝑛𝑔
Area of one filter = 1,000 : 2,000 m2
L=(1:1.25)b and both L, b are ≤ 50m
Operation 2:5 months
Cleaning (removing skin) 1: 15 days depends on shift
Preparation (forming dirty skin) 1:3 weeks
Example:
Design SSF for a water treatment plant working 16 hr/day if the design flow is
32,000 m3/day, if the rate of filtration (R.O.F) is 6 m
3/m
2/day?
Since the working hours is 16 per day then every hour the flow is
32,000 m3/day
16 hr/day = 2,000 m
3/hr
Then the surface area (S.A)
S.A = 2,000
m3
hr∗24hr/day
6 m3/m2/day = 8,000 m
2
Note: when using R.O.F always use the day as 24 hrs nevertheless the
filtration working hours
Assume filter area is 2,000 m2 .. thus we need 4 filters
No of filters = total area/ area of each filter = 8,000/2,000 = 4 filters
Since L = 1.25 b then
Then 2,000 = 1.25 b2
.. thus b = 40 m
Then L = 50m
Thus the final desing is 4 filters... (40*50m)
Note: For stand by during cleaning use 2 filters with same dimensions
Section VIII
96
Rapid-sand filter (R.S.F):
- it consists of larger sand grains supported by gravel and capture particles
throughout the bed.
- Most popular nowadays
- They are cleaned by backwashing water through the bed to 'lift out' the
particles.
- Filtration rate 2 gal/ft2/min., a dual media filter with a rate of 4-6 gal/ft
2/min.
multimedia filter with a rate of 7-10 gal/ft2/min
- Can be
e- single media (usually sand)
f- Double media (sand and anthracite)
g- Multimedia (sand, anthracite , granular activated carbon, and ilmenite)
- Advantages: higher loading rate;
- Water need pre-treatment to stabilize particle charges
Operation procedures:
1- Preparation phase:
a- Open the backwash water from bottom to release the escaped air
b- Open the inlet valve (from top) for 15 min to form a stick layer
2- Filtration phase:
a- Open the waste valve and open the effluent valve and use the water
b- This phase continue for 12:24 hrs depending on water quality
3- Wash phase:
a- After filtration the voids (فجوات) will be filled and there is a pressure head
loss, and the effluent water is not clear
Section VIII
97
b- Close the effluent valve and open the waste valve (5 min)
c- Open pressure air valve (bottom) for 5 min
d- Open water back wash valve (water is pressurized) for 10 min
Design data:
R.O.F = 120 : 200 m3/ m
2/ day
Area of one filter = 40:60 m2
L= (1:1.25) b
Note: No stand by filter is required
Section VIII
98
Quantity of wash water:
Rate of washing (R.O.W) =5:6 R.O.F
Time of washing using compressed water is 8:10 min
Thus the required water quantity for washing in a day =
= No of washing time* (R.O.W) * time of washing * total area of filters
= No of washing time * (5:6 R.O.F) * (8:10min)* area of one filter* No of filters.
Example:
Design SSF for a water treatment plant working 16 hr/day if the design flow is
32,000 m3/day, if the rate of filtration (R.O.F) is 120 m
3/m
2/day? If L = 8m?
Daily flow (Qd) = 32,000 m3/day
16 hr/day = 2,000 m
3/hr
Total Surface area = 2,000*24 / 120 = 400 m2
If L= 8m thus b = 8/1.25 = 6.25 m
Thus the single filter area = 8*6.25 = 50 m2
Then no of filters = 400 /50 = 8 filters
If the filters are washed once a day estimate the required water quantity for filters
wash?
R.O.W = 5 ROF = 5 ∗ 120 𝑚3/𝑚2/𝑑𝑎𝑦 = 600 m3/m
2/day
Amount of water = 600 * 400 *10min /(24hr*60min) = 1,666.6 m3/ day
Section VIII
99
Example:
An existing WTP with 10 Rapid sand filters (and two stand by) each filter dimension
is 8*6m with R.O.F = 150 m3/m
2/day. Check if this plant can serve the future
400,000 capita who has maximum daily water consumption rate = 250L/capiat/day?
Current water capacity (Qc) = 150 * 10 * 8*6 = 72,000 m3/day
Required water in the future (Qf) = 250 L
capita.day∗
1m3
1000L∗ 400,000 = 100,000 m3
/day
Thus the water deficit (shortage) = 100,000 – 72,000 = 28,000 m3/day
How many additional filters are required?
Additional Total area required = 𝟐𝟖,𝟎𝟎𝟎 m3/day
150𝑚3
𝑚2.𝑑𝑎𝑦
= 186.7 m2
Additional number of filters = 186.7 / (8*6) = 3.8 = 4 filters
Pressure filters (in Vessel)
- Same as rapid filter but the filter media is in Vessel and under a high pressure
caused by Air
- The R.O.F = 170:480 m3/m
2/day
- They consist of two or more layers of different granular materials, with
different densities. Usually, anthracite coal, sand, and gravel are used.
- The different layers combined may provide more versatile collection than a
single sand layer.
- Because of the differences in densities, the layers stay neatly separated, even
after backwashing
Section VIII
100
Filter backwash:
-Rapid filters, pressure filter – require periodic cleaning to remove accumulated
solids.
-The pressure (head loss) increase with time thus the filter need to backwash
During the cleaning cycle, or backwash, the flow is reversed and a flow rate of
13-20 gals/ft2/min is forced back through the bed to remove accumulated solids
Section VIII
101