WATER: PROPERTIES, STRUCTURE, AND OCCURRENCE IN NATURE 1297
CHEMICAL PROPERTIES OF NATURAL WATERS
Natural waters acquire their chemical characteristics by dis-
solution of and by chemical reactions with solids, liquids,
and gases with which they have come into contact during
the various parts of the hydrologic cycle. Waters vary in
their chemical composition, but these variations are at
least partially understandable if the environmental history
of the water and the chemical reactions of the rock-water-
atmosphere systems are considered. Dissolved mineral matter
is provided by the crustal materials of the earth; water dis-
integrates and dissolves mineral rocks by weathering. Gases
and volatile substances participate in these processes. As
a first approximation, seawater may be interpreted as the
result of a gigantic acid-base titration: acids of volcanoes
(sulfur dioxide, hydrochloric acid, hydrogen sulfide) react-
ing with bases of rocks (oxides, carbonates, silicates). The
composition of fresh water similarly may be represented as
resulting from the interaction of the carbon dioxide of the
atmosphere with mineral rocks. The earth may be regarded
as a heat engine which extracts energy from solar radiation
in order to drive winds, ocean currents, hydrogeochemical
cycles (cycles of water and rocks) and life cycles. Water,
acting as a transport medium as well as a chemical reagent,
gradually converts primary rocks into soil, sediments, and
sedimentary rocks (Figure 9).
Weathering Processes
Dissolution reactions due to weathering take place because
many constituents of the earth’s crust are thermodynamically
unstable in the presence of water and the atmosphere. Most
important among the weathering reactions is the incongruent
–20^020406080100
Temperature [°C]
0.1
0.2
0.3
0.4
0.5
0.6
0.7
0.8
0.9
1.0
Pressure [bar]
0
0.01
0.02
0.03
0.04
0.05
–10 0 10 20
VAPOR
LIQUID
WATER
ICE I
TRIPLE
POINT
FIGURE 6 The vapor pressure of ice and liquid wa-
ter as a function of temperature. The inset shows the
vicinity of the triple point. (Data from Eisenberg and
Kauzmann, 1969.)
(^0204060)
60
70
80
80
90
100
Temperature [°C]
50
Dielectric Constant
FIGURE 7 The dielectric constant of water as a
function of temperature. (Data from Malmberg and
Maryott, 1956.)
0
0
0.5
1.0
1.5
2.0
20 40 60 80 100
Temperature [°C]
Viscosity [centipoise]
FIGURE 8 The shear viscosity of water as a func-
tion of temperature. (1 centipoise = 10−3 N s m−2).
(Data from Stokes and Millis, 1965.)
where t is the shear stress (force in the x -direction per unit
area normal to z) to maintain the velocity gradient d v x dz in
the z-direction, in the fluid of viscosity m. The viscosity of
water approximately doubles in the range between 25C and
0 C (Figure 8).
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