3.1 Density:
Specific weight g represents the force exerted by
gravity on a unit volume of fluid, and therefore must have the units of force
per unit volume, such as pounds per cubic foot (N/m3 in SI
units). Density and specific weight of a fluid are related as:
Since
the physical equations are dimensionally homogeneous, the dimensions of density
in SI units are:
So,
Note that density
is absolute,
since it depends on mass, which is independent of location. Specific weight
, on the other
hand, is not absolute, since it depends on the value of the gravitational
acceleration g, which varies with location, primarily latitude and
elevation above mean sea level. In general, density of a fluid decreases with increase in
temperature. It increases with increase in pressure but density is highly
variable in gases nearly proportional to the pressure and the density of
liquids depends more strongly on temperature than it does on pressure.
Ideal gas equation of state:
The above equation is used to find the density of any
fluid, if the pressure (P) and temperature (T) are known.
Any equation that relates the pressure, temperature,
and specific volume of a substance is called an equation of state. It is
experimentally observed that at a low pressure the volume o f a gas is
proportional to its temperature.
R is the gas universal constant, and it is different
for each gas R = 8.314 (kJ/kmol.K).
3.2 Specific Weight:
Specific weight is the weight possessed by unit volume of a fluid. It is denoted by (
Specific weight g of pure water as a function of temperature and pressure for the condition where g = 9.81 m/s2
3.3 Viscosity:
The
viscosity a fluid is a measure of its resistance to shear or angular
deformation. Motor oil, for example, has high viscosity and resistance to
shear, is cohesive, and feels “sticky,” whereas gasoline has low viscosity. The
friction forces in flowing fluid result from the cohesion and momentum
interchange between molecules
Figure
4 indicates how the viscosities of typical fluids depend on temperature. As the
temperature increases, the viscosities of all liquids decrease, while the
viscosities of all gases increase. This is because the force of cohesion, which
diminishes with temperature, predominates with liquids, while with gases the
predominating factor is the interchange of molecules between the layers of
different velocities. Thus a rapidly-moving gas molecule shifting into a slower
moving layer tends to speed up the latter. And a slow-moving molecule entering
a faster-moving layer tends to slow down the faster-moving layer. This
molecular interchange sets up a shear, or produces a friction force between
adjacent layers. At higher temperatures molecular activity increases, so
causing the viscosity of gases to
increase with temperature.
Fig
4 a graphically present numerical values of absolute and kinematic viscosities
for a variety of liquids and gases, and show how they vary with temperature.
Consider
the classic case of two parallel plates (Fig. 5), sufficiently large that we
can neglect edge conditions, a small distance Y apart, with fluid filling the
space between. The lower plate is stationary, while the upper one moves
parallel to it with a velocity U due to a force F corresponding to some
area A of the moving plate. At boundaries, particles of fluid adhere to
the walls, and so their velocities are zero relative to the wall. This
so-called no-slip condition occurs with all viscous fluids. Thus in Fig.
5 the fluid velocities must be U where in contact with the plate at the upper
boundary and zero at the lower boundary. We call the form of the velocity
variation with distance between these two extremes, as depicted in Fig. 5, a velocity
profile. If the separation distance Y is not too great, if the velocity U is
not too high, and if there is no net flow of fluid through the space, the
velocity profile will be linear, as in Fig. 5a. If, in addition, there is a
small amount of bulk fluid transport between the plates, as could result from
pressure-fed lubrication for example, the velocity profile becomes the sum of the
previous linear profile plus a parabolic profile (Fig. 5b); the parabolic
additions to (or subtractions from) the linear profile are zero at the walls
(plates) and maximum at the centerline. The behavior of the fluid is much as if
it consisted of a series of thin layers, each of which slips a little relative
to the next.
Fig-5
For a large class of fluids under the conditions of
Fig. 5a, experiments have shown that
We see from similar triangles that we can replace U/Y
by the velocity gradient. If we now introduce a constant of proportionality
(mu), we can express the shearing stress
(tau) between any two thin sheets of fluid by:
This equation called ‘’Newton’s equation of viscosity’’
v Viscosity of liquids
& gases:
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