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Water

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Title: Water


1
Water
  • Chapter 19

2
Hard Water
  • Hard water is water that does not form a lather
    easily with soap.
  • There are 2 types of hardness.
  • 1. Temporary hardness is referred to as hardness
    in water which can be removed by boiling.
  • 2. Permanent hardness cannot be removed by
    boiling.

3
Water hardness in Irelands
4
Temporary Hardness
  • Temporary hardness is caused by the presence in
    the water of calcium hydrogencarbonate Ca(HCO3)2
    and magnesium hydrogencarbonate Mg(HCO3)2.
  • This form of hardness arises when rain water,
    containing the weak acid carbonic acid (H2CO3),
    runs over limestone rocks(CaCO3 ) dissolving out
    Ca2 according to
  • CaCO3 HCO3 H ? Ca(HCO3)2
  • The dissolved Ca(HCO3)2 is now responsible for
    the temporary hardness.

5
  • Scale
  • When this hard water is boiled a reaction occurs
    which results in the
  • calcium ions being precipitated out of solution
    in the form of CaCO3
  • which is almost insoluble. This precipitate forms
    the deposit called
  • scale or fur which is often clearly visible
    on the inside of kettles and
  • boilers in hard-water regions.
  • heat
  • Ca(HCO3)2(aq). ? CaCO3(s) H2O(l)
    CO2(g)

heat Ca(HCO3)2(aq). ? CaCO3(s) H2O(l)
CO2(g)
6
Water softening.
Any process which removes or reduces the degree
of hardness of a water sample is termed water
softening. Boiling a sample of water which has
temporary hardness is an example of a water
softening method.
7
Permanent Hardness
  • Permanent hardness cannot be removed by boiling .
  • Permanent hardness is caused by the presence of
    dissolved calcium and magnesium sulphates and
    calcium and magnesium chlorides. CaSO4 CaCl2
  • An example of how this type of hardness can be
    acquired by water is where water is flowing
    through, or over, gypsum rocks (calcium
    sulphate). The calcium sulphate is slightly
    soluble in water and so the water contains
    dissolved calcium sulphate after passing through
    the rocks, giving a hardness of up to about 500
    p.p.m., again recorded as 500 p.p.m. CaCO3.
  • The sum of the temporary hardness and the
    permanent hardness is referred to as the total
    hardness.

8
  • A number of methods are used for removing
    hardness.
  • Distillation
  • 2. Addition of washing soda

9
3. Ion Exchange resins and de-ionisers. 4.
Calgon
10
Estimation of the Total Hardness in Water
  • This titration involves titrating a sample of
    water (usually but not
  • always 100 cm3) with a solution of disodium
  • ethylenediaminetetraacetic acid (Na2edta) in the
    presence of a
  • buffer which holds the pH at about 10.
  • Na2edta Ca2 ?. Caedta 2Na
  • The indicator is Eriochrome Black T and it
    changes colour at the
  • end-point from wine-red to blue.
  • An unusual feature is that the indicator is added
    as a tiny pinch of solid.

11
Total Hardness
Blue
Wine Red
12
Calculations
  • The calculation involves application of the
  • formula
  • where V volume, M molarity, n number of
    moles in the balanced equation.
  • Having got the molarity of the Ca2 ions, express
    this as moles CaCO3 per litre and then as mg per
    litre, i.e. parts per million (p.p.m.)

13
Water Treatment
14
Water Treatment
  • The various stages of water treatment are.
  • 1. Screening- removal of large particles
  • 2. Settling
  • The precipitation of the particles causing
    turbidity is achieved using
  • flocullation agents. The most common
    flocullation agent is are
  • aluminium sulphate, Al2(SO4)3.
  • Polyelectrolytes are often added to speed up
    flocculation or
  • coagulation. Aluminium contamination is probably
    the most
  • controversial of these agents there has been
  • ongoing speculation linking it with
    neurodegenerative diseases
  • such as Alzheimers disease.

15
Flocullation
floc floating at the surface of a basin
16
Mechanical system to push floc out of the water
basin
17
Filtration Chlorination
  • 3. Filtration
  • The purpose of filtration is to remove particles
    from the water, whether
  • these exist in the raw water naturally or whether
    they have been produced
  • by the coagulation process. Filtration is usually
    achieved by the downward
  • passage of water through about a metre of finely
    divided inert material
  • (sand or anthracite) which is on a support bed
    of coarser material
  • (usually gravel). Drains at the bottom of the
    filter collect the water as it
  • filters through.
  • 4.Chlorination
  • Elemental chlorine and compounds of chlorine are
    regularly added to
  • water during the treatment of the water for
    public supplies. Chlorination is
  • one of a number of possible treatments whose
    purpose is to disinfect the
  • water to keep the pathogen content down to a safe
    level.

18
Filtration
19
5. Fluoridation
  • Fluoridation
  • Over the past forty years a number of studies
    have shown
  • some correlation between fluoride concentration
    in water
  • and the incidence of tooth decay. It would appear
    that at
  • fluoride concentrations of around 1.0 p.p.m.
    Maximum
  • benefit is obtained. The chemicals added to water
    to supply
  • fluoride ion include simple salts such as sodium
    fluoride,
  • NaF, and calcium fluoride, CaF2.

20
Sewage treatment(Waste water treatment)
  • Two measuring parameters are regularly used in
    analysis of wastewater effluent. These are
    Biochemical oxygen demand (BOD) and chemical
    oxygen demand (COD)
  • Biochemical oxygen demand (BOD) is taken as a
    measure of the degree of pollution of a water
    sample based on the quantity of oxygen consumed
    by the micro organisms present in a one litre
    sample stored in the dark at 20 C for five days.
    It can be expressed in milligrams of oxygen per
    litre of sample, i.e. mg l 1 or p.p.m.

21
Activated sludge
22
Primary Treatment(Physical)
  • Pre-treatment
  • The incoming sewage is pushed through
    mechanically raked screens to macerate the sewage
    and remove large debris.
  • The pre-treated sewage flows into primary
    settling tanks. The sewage enters at the centre
    of the tank, (c. 12 m in diameter and c. 2 m
    deep), and rises allowing sludge to settle.
  • The decanting liquid is transferred to the
    secondary treatment system. The settling tanks
    have a skimmer mechanism at the top to remove
    floating particles and a scraper on the settling
    tank floor (the base of the tank is
    hopper-shaped, i.e. sloping to the centre) to
    gather the settling sludge.

23
Primary
Solids and large floating debris are screened
from the waste water  Remaining solids are
removed by allowing the waste to settle in
sedimentation tanks
24
Secondary Treatment(Biological)
  • This involves the biological degradation of the
    nutrient content of the effluent. This is usually
    done aerobically using percolating filters,
    activated sludge digestion units, aeration basins
    or biotowers.
  • Percolating filters and activated sludge
    digestion units are commonly used in sewage works
    but all four methods can be found in use
    separately or in pairs industrially.

25
Secondary Treatment
Activated Sludge Method The activated sludge
method operates aerobically. The sewage is fed
continuously into aerated tanks that is kept
oxygenated by mechanical agitators. The
micro-organisms break down the organic material
into Carbon Dioxide and Water.
26
Waste water treatment plant
27
Tertiary Treatment(Nitrates and Phosphates)
  • While primary and secondary treatment of effluent
    largely
  • concentrate on the reduction of COD/BOD levels
    they have a
  • lesser impact on phosphate and nitrate
    concentrations under the
  • conditions normally applied. High levels of
    nitrogen and
  • phosphorus are environmentally harmful as they
    act as nutrients
  • which give rise to algal bloom, leading to
    eutrophication.
  • Ammonium salts and nitrates are the common
    sources of nitrogen
  • and usually originate from animal waste or
    fertilisers.
  • Phosphates are precipitated by treatment with
    lime, Ca(OH)2,
  • aluminium sulphate, Al2(SO4)3, or
    iron(III)sulphate, Fe2(SO4)3. In
  • each case an insoluble salt is produced which can
    be filtered off.

28
Tertiary Treatment(Nitrates and Phosphates)
Removal of nitrates and phosphates   Phosphates
are removed by precipitation with Aluminium
Phosphate   Nitrates are removed by biological
nitrification. Tertiary treatment is a costly
process
29
Water pollution
  • Eutrophication.
  • The over-enrichment of waters by nutrients, such
    as nitrate and phosphate, gives rise to a problem
    known as eutrophication.
  • Added nutrients act as fertilisers and result in
    increased growth of algae and other plant matter
    in waterways. This increased growth is often very
    apparent from algal blooms and scums on stretches
    of waterways.
  • When this type of algal bloom is followed by
    death and decay of
  • animal and plant life in a competition for
    depleting oxygen
  • supplies,the term eutrophication is used.

30
Eutrophication
Fish Kill in the Salton Sea as a result of
eutrophication
Algal bloom in Orielton Lagoon, Australia,
31
Suspended and Dissolved Solids
  • Suspended solids can be particles of plant and
    animal remains or silt.
  • These neither sink nor float they are held in
    suspension in the liquid
  • but are not dissolved.
  • The amount of suspended solids in a sample of
    water can be
  • determined by weighing a dried sheet of fine
    grade filter paper and
  • filtering through it a known volume of water (a
    reasonably large volume of
  • water will usually be needed, e.g. one litre).
    The filter paper is then
  • washed with distilled water, dried carefully and
    reweighed. The increase
  • in mass is the mass of solids suspended in the
    sample.
  • Suspended solids are usually expressed in p.p.m.

32
Total Dissolved solids
  • The dissolved solids can be determined by taking
    a known volume
  • of filtered water (to ensure that all suspended
    solids have been
  • removed) in a previously weighed dry beaker, and
    then boiling the
  • contents gently to dryness.
  • The dissolved solids will remain in the beaker
    and their mass can
  • be accurately found by reweighing the beaker when
    it has cooled.
  • The concentration of dissolved solids should also
    be expressed in p.p.m.

33
Estimation of Dissolved Oxygen in Water
  • Estimation of the concentration of dissolved
    oxygen in water is
  • used in the determination of the quality of
    surface waters and also
  • in waste waters, particularly from biological
    treatment plants.
  • The most common titrimetric procedure to measure
    dissolved
  • oxygen is called the Winkler method. It relies on
    reactions involving
  • manganese ions, iodide ions and oxygen. Under
    alkaline conditions
  • the oxygen dissolved in the water oxidises the
    Mn2 ions to Mn3
  • ions. When the mixture is acidified, the Mn3
    ions are reduced
  • back to Mn2 ions by the iodide ions.
  • This reaction liberates iodine whose
    concentration can be estimated
  • by titration against standard sodium thiosulphate
    solution. The
  • concentration of the iodine in the final solution
    is twice the oxygen
  • concentration of the original solution.

34
Winkler method
35
Biochemical Oxygen Demand (BOD)
  • Biochemical Oxygen Demand (BOD)
  • The BOD test was first devised by the Royal
    Commission on Sewage in the early 1900s.
  • The biochemical oxygen demand is the amount of
    dissolved oxygen consumed by biochemical action
    when a sample of water is kept in the dark at 20
    C for five days.
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