Nidhi
H. No. 560/29, Tilak
nagar, Rohtak
*Corresponding Author
E-mail: jitender.dhull1982@gmail.com
ABSTRACT:
Water is an indispensable need of life and ground water has become
a global problem partly because of population explosion and partly due to phenomenal advances in industrialization. First check Ca2+
and Mg+ F-1, Cl-,
Na, PH, Electronic conductivity TDS, Hardness of drinking water surrounding
villages of Jhajjar District Check the potability of
drinking water
KEY WORDS:
INTRODUCTION:
Water in the most abundant substance of
living being. It forms
70-80% of cells and 70% of human body. In seeds and spores the content of water
is as low as 10-20%. About 95% of water occurs in the free
state while the remaining 5% is found in the bound and combined state.
Water has maximum solvent power 10 compared to other liquids:
Non-polar substance can be dispersed by water due to two reasons.
(a) In association with other polar materials.
(b) In the hole of lattice aggregate the small
amount of water is in the ionic state.
H2O H+ +
OH-
Water is ideal medium of chemical reaction. It is product of
respiration. Water has high thermal conductivity water cycle consists of two
overlapping cycles lager global and smaller global. Global water cycle consists
of evaporation and precipitation of water.
One estimate put the world precipitation state at 4.46 × 1020g
per year. This means that the atmosphere must be refilled with the water vapours 34 times in years. Aquatic
animals absorbs water from the surroundings and excrete it after the
death of organisms water returns to the surrounding medium through three
process of decay.
Water classified as “hard’ and “Soft” water concentration of
calcium and Magnesium ions is high, the capacity of lather is reduced is this
is “hard water.” A soft water which produce lather easily.
Global Distribution of Fresh
Water
|
Sr. No. |
Fresh water |
Expressed in
Cubic Kms. |
|
1. |
Water in ice
sheets, snow cope and glaciers etc. |
24,000,000 |
|
2. |
Ponds, lakes and
reservoirs |
280,000 |
|
3. |
Streams and
rivers |
1,200 |
|
4. |
Soil moisture |
85,000 |
|
5. |
Ground water and
well water |
60,000,000 |
|
|
Total amount of
fresh water |
84,366,200 |
The use of water can be considered under
two categories namely.
(i) Consumptive and partially consumptive
(ii) Non consumptive.
The first category comprises such uses as domestic water supply
irrigation and requirement of industries and power generation with fossil and
nuclear fuels.
The second category encompasses hydropower, generation,
navigation, pisciculture, recreation wild life
preservation and river conservancy. Almost 76% of total used by man has to utilized to grow food following agriculture. Power generation (6.2%) and industries (5.5%) domestic requirement
and stock management taken together (4.67%) of total drawn. A large
fraction is returned to the surface deposits or stream flows often in a
polluted stated which can be reused as such or after treatment to remove
impurities out of the total quantity of water drawn the amount of water
irrecoverable consumed was estimated to be about 2,200 cubic kms. (L’ vovich 1989) the
approximate requirement of fresh water in India as estimated for the year 1974
A.D., 2000 A.D. and
2025 A.D.
|
Water herd |
1974 |
2000 |
2025 |
|
Irrigation |
350.0 |
630.0 |
770.0 |
|
Thermal power generation |
11.0 |
60.0 |
160.0 |
|
Industries |
5.5 |
30.0 |
120.0 |
|
Domestic
requirement |
8.8 |
26.6 |
39.0 |
|
Lince
stock management |
4.7 |
7.4 |
11.0 |
|
Total |
38.0 |
754.0 |
1,1000 |
Potable Water
The water which is safe to drink is potable water. However does
mean distilled or pure water. Potable water fit for human consumption, should
satisfy the following essential requirement.
(1) It should be sparking clear and orderless.
(2) Pleasant in taste.
(3) Perfectly cool
(4) Turbidity should not exceed 10ppm.
(5) It should free from objectionable dissolved
gases like H2S.
Technique employed the analyses of water
Polythene bottles of 2.5 litre capacity
are used as sample container.
Sampling Techniques
For the analysis of ground water, two principal types of sapling
procedures13/14 are employed.
1. Spot or Grab samples sport samples are
discrete portions of water samples taken at a given time. A series of grab
samples, collected from different depths at a given site, reflect variations in
constituents are period of time.
2. composite samples when the grab samples of a particular water is collected at a regular interval for a
specific period such as 12 hours or 24 hours and mixed, then the integrated
sample is called composite sample.
When liquid is homogeneous, it is sufficient take the grab sample
only. The sample bottle should first be rinsed with the liquid being sampled
and then filled.
When liquid to be sampled is heterogeneous such as sewage a
composite sample is necessary of any constituent to be determined is affected
by air contact take the sample out of contact with air and completely fill the
container when hot sample are taken they must be cooled using cooling coils. The
tap should be cleaned inside and outside then collect the sample the water
being sample should then be allowed to waste for sometime so that the sample
will be representatives of the whole supply.
Then water from well is collected then well has to be pumped for a
sufficient time such that the sample represent the ground water that feeds the
well. Samples are taken at the mid point of livers
and scheme. Collect samples at least 0.6 to 1 km. below dams or water sample
keep out of light and low temperature (4°C) white. Determination like Ph,
dissolved gases as O2, CO2 and H2S were made
immediately while other constituents analyzed after sometime.
Chemical Substance Affecting
Portability Colour
This test is usually applicable to drinking water and potable
water. It was carried out by comparison with known colour
standard5. Colour in water may be due to
presence of fine particles in suspension or due to certain mineral matter in
solution. Even pure water is not colourless and it
has been found to have a pale green tint in large quantities. The three colour of a water sample is due to the substances present
as fine collides, colour is measured with an
instrument known as tinto meter. The unit of colour is measured on the platinum
cobalt scale and expressed in
Hazen units. The standard colour can be produced by
dissolving 1 mg. of platinum
Cobalt in one litre of double distilled water.
Turbidity
Turbidity in water is due to colloidal and extremely fine
dispersions. Suspended matter such as clay, silt, finely divided organic and
inorganic matter, plankton and other macro-organisms also contribute turbidity.
Turbidity can be measured by visual method and instrumental methods such as absorptiometrically or nephelometically.
The standard unit of turbidity is considered as that produced by one ppm of silica in the form of diatomaceous earth. Turbidity
removed by setting or by centrifuging.
Odour
Odours in water are due to presence of microscopic organisms or
delaying vegetation including algi, fungi, bacteria, actinomycetescets and weeds16. Sewage and
industrials effluents cause offensive odours to
receiving waters. The extent of odour depends upon
the pH of water-lower the pH higher will be the amount of
hydrogen sulphide
produced.
For example, the protozoa, dinobryon
imparts a fishy odour in water. The algae oscilltory and rivularia produce mouldly odour and algae anabaena
a strong grassy odour. Mineral matters such as sand
and clay when present in finely divided state produce a faint earthy taste and odour in water.
To determine the hot odour quality take
250ml sample in a 500ml stoppered conical flask and
heat to 58-60°C. Sniff the odour which may be:
(i) Aromatic
(ii) Chlorinous
(iii) Chemical (iv) Medicinal
(v) Sulphuretted (vi) Septic
(vii) Earthy (viii) Peaty
(xi) Grassy (x) Moldy
(xi) Fishy (xii) Disagreeable
(xiii) Vegetable (xiv) Putrid
(xv) Wormy
The intensity of odour is expressed in
terms of Threshold Odour Number. For drinking water
TON should not exceed three.
Taste
Taste is always accompanied by odour.
However, dissolved mineral matters produce tastes but not odour.
A faint bitter taste may be due to the presence of sulphate while soapy or inky
taste may be due to excess of sodium carbonate. Water containing unusual salt
content have a brackish taste. Dissolved gases,
minerals, nitrates and carbonic acid make water palatable.
Temperature
Surface waters differ considerably in temperature between winter
and summer. Temperature measurements are useful in detecting an unsuspected source
of pollution, in calculating alkalinity and in industrial water supplies for
heat transmission calculations Hydrogen Ion concentration (pH).
pH, a measure of hydrogen ion activity, is used to express the
intensity of acidic or alkaline condition of a solution. it is also an
important factor water to 100ml in volumetric flask at 25°C.
pH
7 Buffer Solution
dissolve 1.361g anhydrous potassium dihydrogen
phosphate (KH2PO4) and 1.420g sodium dihydrogen
phosphate (NaH2PO4) in distilled water and make up to
1000ml in a volumetric flask.
pH
9 buffer solution
dissolve 3.81 borax (Na2B4O7.10H2O)
in distilled water to 1000ml.
(i) The desirable pH range for drinking waters
is 7.0 to 8.5.
(ii) pH in conjunction with total salinity and
temperature is used to determine whether a water is corrosive in nature or
having scale forming tendencies.
Electrometric Method for the
Determination of pH
Electrometric determination of pH involves the measurement of
(EME) of a cell comprising an indicator electrode (glass electrode) responsive
to hydrogen ions and a reference electrode (calomel electrode)
pH
4 Buffer Solution
dissolve 1.012 anhydrous potassium hydrogen phthalate in distilled.
Its unit is micromhos/cm or micro siemns/cm3.
Conductity of water varies directly with the
temperature and is proportional to its dissolved mineral matter content.
Specific Conductance
specific conductance is the conductance of one centimeter cube of a
solution of an electrolyte. It is generally denoted by k (Kappa) thus
k = 1/P
A simple conductivity meter with dip-type cell was used for the
analysis of water samples. The instrument and the cell was calibrated by using
0.005M KCI solution (Conductivity = 654 mho cm-1).
Acidity
Mineral Acidity
Took 50ml or suitable dechlorinated
aliquot of the sample in a 250ml conical flask. Added 2 drops of methyl orange indicator
and titrated with 0.02N-NaOH solution till faint orange colour.
Calculation
Acidity as CaCO3
mg/L =
Results
Methyl orange acidity value shows mineral acidity. In absence of
mineral acidity, total acidity is only the CO2 acidity of the water
sample.
Alkalinity
Alkalinity of water is due to the presence of carbonate and
hydroxide ions. Determination of alkalinity by Titrimetric method principle alkalinity was
determined by titration with 0.02 NH2SO4 using methyl
orange and phenolphthalein as indicators.20
Reactions
2CaCO3 + H2SO4 CaSO4 + Ca(HCO3)2
Ca(HCO3) + H2SO4
CaSO4 + 2CO2 + 2H2O
Ca(OH)2 + H2SO4 CaSO4
+ 2H2O
Total hardness (Ca and Mg)
The hardness of water is not a pollution
parameter but indicates water quality, mainly in terms of Ca2+ and
Mg2+, expressed as CaCO3. The analysis is done by complexometric titration.21,22
Classification
of Hardness
Hardness has traditionally been divided
into temporary and permanent hardness.
Temporary
Hardness
The portion of hardness which disappears on
prolonged boiling is called temporary, hardness. It is caused by bicarbonates
of Ca2+ and Mg2+.
Permanent
Hardness
The hardness that remains after boiling is
called permanent hardness. It is caused by the presence of sulphate,
chlorides, nitrates of Ca2+ and Mg2+.
Determination
of total hardness
Principle
During titration with EDTA (Na2H2Y),
Ca2+ first reacts to form relatively stable CaY2-,
followed by Mg2+ to give MgY2- complex (indicator/wine
red) releasing the free indicator (blue). The colour
changes from wine-red to blue at the end point.
Reaction
Eriochrome Black T
{1-(1-Hydroxy-2-naphthylzao-6-nitro-2-naphthol-4-sulphonate)}
This gives total Ca2+ and Mg2+
Next from a aliquot of the sample, Ca2+ is estimated selectivity at
pH 12.3 (Mg2+ gets precipitated as Mg(OH)2 in presence of
cation indicator. The colour
change is from pink to blue.
Calcon
[1-2
(Hydroxy-1-naphthylzao)-2-naphthol-4-sulphonate]
Total hardness (Ca and Mg)
Total hardness of water is not pollution
parameter but indicates water quality in term of Ca2+ and Mg2+
expressed as CaCO3. The total hardness is also expressed in ppm. The analyses is done by complexometric titration using EDTA. The hardness of water
reflects the nature of geological formation with which the water is in
contract. Ground water30 may be hard due to the natural accumulation
of salts from contract with the soil. Generally surface water are softer than ground well waters. Total hardness is
calculated by adding the multi equivalents of Ca and Mg per litre
and multiplying the sum by 50.
According to the degree of hardness the
waters are commonly classfied31 as per U.S. Geological survey as
illustrated in table.
Table : Classification of
Hardness
|
Total hardness as CaCO3 in mgk |
Classification |
|
0-55 |
Soft |
|
50-100 |
Slightly hard |
|
101-200 |
Moderately hard |
|
201-500 |
Very hard |
On examining the table total hardness value ranges in between 100
to 4300ppm. These results indicate that the ground water of this region in very
hard in nature. Hard water of these wells are reported
to cause no harmful effect upon the health of consumers. The use of hard waters
however is limited because of excessive soap consumption in homes. Hard water
form incrustation untensils and the vegetables cooked
in it get toughened.
Total
dissolved solids
In natural waters, the dissolved Solids consist mainly of
bicarbonates, carbonates, chlorides, sulphate,
nitrate and possibly phosphates of calcium, magnesium, sodium and potassium
with traces of iron and other substances. In the percent study the total
dissolved solids range between 120 to 40,700 ppm in
the water samples. The WHO International32 standards set the
permissible33 limit for total dissolved solids as 1000 ppm and excessive limit as 3000ppm. Thus water for domestic
and industrial uses should have TDS value of less than 1000ppm. And for
agriculture utility the optimum range should be below 3000ppm. In the percent
investigation the TDS value lies between 175 to 4300 ppm.
Sodium
Sodium is a major component of potable waters. Most of the sodium
compounds are water soluble and do not play any role in the incrustation of
wells. The primary sauce of sodium in natural water is from the release of
soluble products – All natural waters contain meouble34 amount of
sodium.
Calcium
Calcium is an essential element and human body requires
approximately 0.7 to 2.0g of calcium per day as a food element. However waters
with high calcium content are undesirable for washing, bathing and laundering
because of the consumption of more soap and other clearing gents sub surface
waters in contact with sedimentary35 rocks of marine origin drive
most of their calcium for the
solution of dolomite, anhydrite and gypsum.
Surface water in equilibrium with atmospheric carbon dioxide can
contain as much as 20ppm to 30ppm of calcium at saturation. In the present in
investigation the calcium concentration lies between 24 to 1544 ppm.
Magnesium
Magnesium is an essential element for human beings. Magnesium is
relatively non-toxic to man. However, a higher concentration causes unpleasant
taste to water. At high concentrations, magnesium salts have a laxative effect
particularly when present as magnesium sulphate.
Despite higher solublities of most of
the magnesium compounds, magnesium is generally found in lesser amount in
natural than is calcium. In contrast with most natural water, sea water
contains above five times as much magnesium as
calcium. The deficiency of calcium in sea water is undoubtedly due to the
preferential abstraction of calcium by plants and animals.
Common concentration of magnesium range from about 1 to 40 ppm, water from rocks rich in magnesium may have as much as
100ppm, but concentrations more than 100 ppm rarely
encountered except in sea water and brines. Exceptionally low values of calcium
and magnesium are found in some waters which have undergone natural softening
by cation exchange.
Fluoride
Source of fluoride in ground water are minerals like calcium
fluoride, apatite cryohite and fluorspar in sedentary
rocks. Presence of fluoride in drinking water in beneficial36
because it reduces tooth decay. At higher levels, however mettling of the teeth occurs. For this reason maximum fluoride
concentrations recommended for drinking water as per WHO or ICMR standards
range from 1.4 to 2.4ppm depending on how much water is ingested. In the
present investigation the fluoride concentration ranges in between 0.1 to 1.85 ppm.
Chloride
Chloride is a major dissolved constituents
of most natural water. The concentration of C1 ions varies team sample to
sample under investigation. Chloride produces a salty taste to all well waters,
but the salty taste is variable. Reasonable amounts of chloride are tolerable
in many water supplies. Chloride salts are highly soluble in water so they can not be removed simply by precipitation.
Chloride is also free from the effects of exchange, adsorption and
biological activity. Chloride concentration found in natural
water vary between 0.1 ppm in arctic snow to
150,000 ppm in brines. Continental37 rain
and snow may contain from 1.0 to 3.0 ppm of chloride.
1.village –
dighal
pH 7.9
E.C(µmhos/cm) 1500
TDS 380ppm
Hardness 280ppm
Ca2+ 52.0ppm
Mg2+ 36.0ppm
Cl- 90ppm
Na+ 6.8ppm
Result – water
is potable here. All constituents present within the limit.
|
2. VILLAGE – GUDDA |
|
|
pH |
8.4 |
|
E.C |
3700 |
|
TDS |
90 |
|
Total Hardness |
460 |
|
Ca2+ |
96.0 |
|
Mg2+ |
50.8 |
|
Cl- |
150 |
|
Na+ |
17.8 |
Result: water is potable here.
|
3.
VILLAGE -
SHERIA |
|
|
pH |
8.0 |
|
E.C |
1000 |
|
TDS |
640 |
|
Total Hardness |
400 |
|
Ca2+ |
76.0 |
|
Mg2+ |
38.0 |
|
Cl- |
240 |
|
Na+ |
4.4 |
Result:
As all the value lies within the limit. Thus
sample is potable.
Suggestions and Conclusions:
Water is an indispensable need39-41 of life. We are now
near the stage when surface and ground water has become a global problem partly
because of the population explosion and partly due to phenomenal advances in
industrialization. Now there is the need to prevent water borne diseases such
as typhoid, chlorea, diarrhea and dysentery etc. The
water quality of wells needs a betterment in which can be achieved by
considering the following suggestions :-
1. The contaminant sources near the wells
should be carefully surveyed so that there is no seepage of toxic constituents.
2.
Location
of wells for drinking water supplies should be decided with utmost caution.
3.
Surrounding
contaminant’s sources and flow direction of effluents should be considered.
4.
It is
not advisable to tap the uppermost acquifer in case
of drinking wells.
5.
Location
of industrial and municipal disposal sites should be decided keeping in view
the ground (well) water levels and flow patter in the area.
6.
In
case of toxic industrial effluents, steps should be taken for predisposal
treatment by the industry itself.
7.
Industries
must also learn to do a better job of controlling the release of its pollutants
or thermal discharges.
8.
The 4R
concept i.e., recycling, renovation, recharge and reuse should be employed in
the modern technology of waste water treatment.
9.
All
disposal of solid wastes near the well waters or the various channels need to
be curtailed.
10.
Most
of the municipalities still use the inadequate primary treatment. So there is
an urgent need to design sewage treatment facilities so that BOD load on
receiving water is reduced.
11.
Water
quality of the wells rivers need to be monitored and
controlled in a sustained manner for human use and sustenance of the ecosystem.
12. More treatment plants should be created for
treatment of effluents. Discharge of raw sewage, sullage
and sludge should not be allowed in the water bodies.
References:
1.
Nag B.S. and Kathapalia G.N.,
Water resources of India. Second World congress of water resources. Report of
the irrigation Commission, Ministry of Irrigation and Power, New Delhi Vol. 3,
1975.
2.
Vaidyanthan A., Water
Resources, what we do not now? The Hindu survey of environment, Madras, 1994.
3.
Vohra B.B., Managing
India’s water resources INTACH Environmental Series-II, New Delhi, 1990.
4.
Rogers P.P., Freshwater. In the Global possible: Resource,
development and the new century. Ed. Repetto R., App.
E.W. Press, New Delhi, 1991.
5.
Lvovitch M.J., World water
resources and their future. English translation. Ed. R.L. Nace,
American Geophysical Union, Washington D.C., 1979.
6.
Peixoto J.P., Kettani M.A., The control of water cycle. Scientific
American, 228(4), 46, 1973.
7.
Kathpalia G., Water
budgeting and Planning. In water pollution and
management Ed. Varshney C.K., Wiley Eastern Ltd., New
Delhi, 1985.
8.
Desarda H.M., Irrigation
planning, water its economic and politics. In the
Hindu survey of Environment, Madras, 1994.
9.
Sandra Postel, Manageing
fresh-water supplies. In state of the world, Eds. Brown LR., et al., Prentice
Hall, New Delhi, 1985.
10.
Vohra B.B., Agenda for
water, Myth and reality. The Hindu survey of environment, 1998.
11.
Stumn W. and Morgan
J.J., Aquatic Chemistry, Wiley inter science, New York, 1977.
12.
Suffer I., Mcguire M., Josephson,
J. and Ember L., Env. Sci. Tech., 12, 1138, 1978.
13.
American Society for sampling and testing manual on water, 3rd
edition, Philadelphia, 1979.
14.
Black H.H., Procedures for sampling and measuring
industrials wastes, SIWAA, 24, 45, 1972.
15.
Aboo K.M., Shastry
C.A. and Alex P.G., A study of well water in Bhopal city, Indian J. Environ.
Health, 1978.
16.
British standards Institutions, Specification for pH scale,
BS-1647, 1971.
17.
Robinson R.A. and Stokes R.H., Electrolytic solutions,
Second edition, Academic Press, New York, 1979.
18.
Dickinson D., The chemical analysis of waters, boilers and
feed waters, sewage and effluents, Blackie and Son, London, 1980.
19.
Marr I.L. and Gesser M.S.,
Environmental Chemical analysis, International Text Book Co., Glasgow, 1983.
20.
Natusch D.F.S. and Hopke P.K. Analytical aspects of environmental Chemistry,
John Wiley and Sons, New York, 1983.
21.
Vogel A.I., A text book of quantitative inorganic analysis
including elementary analysis LBS Longman, Green and Co. Ltd. London, 1984.
22.
Dean J.A., Flame Photometry, McGraw Hill publishing Co., New
York, 1980.
23.
Kolthoff I.M. and Sandell E.B., Text Book of quantitative inorganic analysis,
McMillan Co., New York, 1992.
24.
Hillebrand W.F., Applied
inorganic analysis, John Wiley and Sons, New York, 1983.
25.
Her Majestry’s stationary office.
Analysis of raw, potable and waste waters, HMSO, London, 1972.
26.
Bis, Drinking
water specifications, Business of India Standard, New Delhi, UDC, 15, 00315,
621, 1991.
27.
American Public Health Association AWWA, water pollution
control federation. Standard methods for the examination of water and waste
water, 19th APHA, Washington, 1995.
28.
Stanely N. Davis, Roger
J.M., Hydrogeology, John Wiley and Sons, New York, 96-125, 1990.
29.
Todd David Ceith, Ground water
hydrology, John Wiley and Sons. Inc. New York, 191, 1959.
30.
Goetx C.A. Loomis T.C.
and Delhi H., Total Hardness in water, Anal. Chem., 22, 798, 1980.
31.
Babbit H.E. and Donald
J.J., Water supply engineering, 5th Ed, McGraw Hill and Co. London,
1955.
32.
Manahan S.E., Environmental Chemistry, Willard Grant Press,
Boston USA, 3rd Ed. 1989.
33.
Edwin Windle Taylor, The
examination of water and water supplies, 6th Ed., Churchill Ltd.,
London, 1989.
34.
Dean J.A., Flame Photometry, McGraw Hill Publishing Co. New
York, 1980.
35.
Marr I.L. and Cresser M.S.
Environmental Chemical analysis, International text book Co. Glasgow, 1983.
36.
Samant H.S., Methods for
chemical analysis of water and waste, Surveillance report EPSS-AR 73-12,
Canada, 1983.
37.
Home R.A., Chemistry of aquatic environment, Wiley Inter
science, 1978.
38.
Ciacci L.L., Water and
water pollution handbook, Marcell Dekker, New York,
1982.
39.
Jackson D.V., et a;., Recovery from
Industrial and domestic wastes in centralized treatment plant. In: Chem. Engg. In a changing world, edited by Koester W.T. (EISEVIEW
scientific Pub. Co. Amsterdam), 1986.
Received on 04.12.2012
Modified on 12.12.2012
Accepted
on 18.12.2012
©
A&V Publication all right reserved
Research J. Science and Tech.
4(6): November –December, 2012: 267-273