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GAS TRANSFER

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Title: GAS TRANSFER


1
GAS TRANSFER
2
DEFINITION AND TERMS
  • Gas transfer ? a physical phenomenon, by which
    gas molecules are exchanged between a liquid and
    a gas at a gas-liquid interface ?
  • (1) an increase of the concentration of the
    gas(es) in the liquid phase as long as this phase
    is not saturated with the gas under the given
    conditions of e.g. pressure, temperature
    (absorption of gas)
  • (2) a decrease when the liquid phase is over
    saturated (desorption, precipitation or stripping
    of gas)

3
DEFINITION AND TERMS
  • Important natural phenomena of gas transfer ? the
    reaeration of surface water
  • (1) the transfer of oxygen into surface water
  • (2) release of oxygen produced by algal
    activities up to a concentration above the
    saturation concentration
  • (3) release of taste and odor-producing
    substances
  • (4) release of methane, hydrogen sulfide under
    anaerobic conditions of surface water or of the
    bottom deposits

4
ELEMENTS OF AERATION AND GAS TRANSFER OPERATIONS
  • Gas transfer occurs only through the gas-liquid
    interface ? has to be carried out as to maximize
    the opportunity of interfacial contact between
    the two phases.
  • The engineering goal ? to accomplish the gas
    transfer with a minimum expenditure of initial
    and operational cost (energy).

5
ELEMENTS OF AERATION AND GAS TRANSFER OPERATIONS
  • Four different types of aerators
  • Gravity aerators
  • (a) cascades ? the available difference head is
    subdivided into several steps
  • (b) inclined planes ? eqipped with riffle plates
    to break up the sheet of water for surface
    renewal
  • (c) vertical stacks ? droplets fall and updrafts
    of air ascend in counter current flow

6
ELEMENTS -- CASCADES
7
ELEMENTS INCLINED PLANES
8
ELEMENTS VERTICAL STACKS
9
ELEMENTS VERTICAL STACKS
10
ELEMENTS VERTICAL STACKS
11
ELEMENTS AMMONIA STRIPPING
12
ELEMENTS OF AERATION AND GAS TRANSFER OPERATIONS
  • (2) Spray aerators
  • ? the water is sprayed in the form of fine
    droplets into the air ? creating a large
    gas-liquid interface for gas transfer

13
ELEMENTS SPRAY AERATORS
14
ELEMENTS OF AERATION AND GAS TRANSFER OPERATIONS
  • (3) Air diffusers (bubble aeration)
  • ? air is injected into water
  • (a) through orifices or nozzles in the air
    piping system
  • (b) through spargers
  • (c) through porous tubes, plates, boxes or domes
  • ? to produce bubbles of various size with
    different interfacial areas per m3 of air.

15
ELEMENTS AIR DIFFUSERS
16
ELEMENTS AIR DIFFUSERS (POROUS TUBES)
17
ELEMENTS AIR DIFFUSERS
18
ELEMENTS AIR DIFFUSERS
19
ELEMENTS AIR DIFFUSERS
20
ELEMENTS OF AERATION AND GAS TRANSFER OPERATIONS
  • (4) Mechanical aerators
  • ? create new gas-liquid interfaces by different
    means and constructions ? two types of
    construction
  • (a) various construction of brushes ? a
    horizontal revolving shaft with combs, blades or
    angles
  • (b) turbine or cone aerators with vertical shaft

21
Boyles Law
22
Charles Law
23
Gay-Lussacs Law
24
Ideal Gas Law
The ideal gas law is a special form of an
equation of state, i.e., an equation relating the
variables that characterize a gas (pressure,
volume, temperature, density, .). The ideal gas
law is applicable to low-density gases.
25
Absolute Zero and the Kelvin Scale
The pressure-temperature relation leads to the
design of a constant-volume gas thermometer.
Extrapolation of measurements made using
different gases leads to the concept of absolute
zero, when the pressure (or volume) is zero.
26
Kinetic Theory Applications
  • Kinetic theory investigates (on a molecular
    scale) topics such as
  • Change of phase (evaporation vapour pressure
    latent heat)
  • Pressure
  • Change of shape and volume (elasticity Hooke's
    law)
  • Transport phenomena (diffusion - transport of
    mass viscosity - transport of momentum
    electrical conduction - transport of electric
    charge thermal conduction - transport of heat)
  • Thermal expansion
  • Surface energy and surface tension

27
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28
Kinetic Theory of Gases Basic Assumptions
  • The number of molecules is large, and the average
    separation between them is large compared with
    their dimensions. This means that the molecules
    occupy a negligible volume in the container.
  • The molecules obey Newton's laws of motion, but
    as a whole they move randomly. 'Randomly' means
    that any molecule can move equally in any
    direction.
  • The molecules undergo elastic collisions with
    each other and with the walls of the container.
    Thus, in the collisions both kinetic energy and
    momentum are constant.
  • The forces between molecules are negligible
    except during a collision. The forces between a
    molecule are short-range, so the molecules
    interact with each other only during a collision.
  • The gas is a pure substance. All molecules are
    identical.

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31
SOLUBILITY OF GASES
  • The solubility of gases in water (and also in
    other liquids) depends upon
  • (1) the nature of the gas generally expressed by
    a gas specific coefficient ? the distribution
    coefficient, kD
  • (2) the concentration of the respective gas in
    the gaseous phase ? related to the partial
    pressure of the respective gas in the gas phase
  • (3) the temperature of the water
  • (4) impurities contained in the water

32
INFLUENCE OF THE GAS CONCENTRATION ON SOLUBILITY
  • The higher the gas concentration in the gaseous
    phase ? the greater will be the saturation
    concentration in the liquid phase
  • The relation between the saturation concentration
    cs (g/m3) and the gas concentration in the gas
    phase cg (g/m3)
  • cs kD . cg

33
INFLUENCE OF THE GAS CONCENTRATION ON SOLUBILITY
  • The molar gas concentration in the gas phase
    (according to the universal gas law)
  • (n/V) p / (RT) (moles/m3)
  • Hence the corresponding mass concentration cg is
    obtained by multiplication with the molecular
    weight (MW) of the gas
  • cg (p . MW)/ (RT) (g/m3)

34
INFLUENCE OF THE GAS CONCENTRATION ON SOLUBILITY
  • The combination yields
  • cs (kD . MW . p)/ (RT)
  • Henrys law is generally written as
  • cs kH . p
  • The relation between distribution coefficient kD
    and Henrys constant
  • kH (kD . MW)/ (RT)

35
INFLUENCE OF THE GAS CONCENTRATION ON SOLUBILITY
  • Bunsen absorption coefficient, kb ? how much gas
    volume (m3), reduced to standard temperature
    (0oC) and pressure (101,3 kPa), can be absorbed
    per unit volume (m3) of water at a partial
    pressure of pO 101,3 kPa of the gas in the gas
    phase
  • cs (m3 STP gas/m3 water) kb

36
INFLUENCE OF THE GAS CONCENTRATION ON SOLUBILITY
  • And any other partial pressure p
  • cs kb . (p/p0) (m3STP/m3)
  • Since 1 m3STP contains p0/R.T0 moles of gas and a
    mass of gas equal to MW. p0/R.T0
  • cs (kb . MW)/(R.T0 ) p (g/m3)

37
INFLUENCE OF THE GAS CONCENTRATION ON SOLUBILITY
  • The relation between kD and kb
  • kb kD T0/T
  • The interrelationship between the three
    coefficients
  • kD kH .R.T/MW kb .T/T0

38
INFLUENCE OF THE GAS CONCENTRATION ON SOLUBILITY
  • In the practice of aeration the gas phase will
    always be saturated with water vapor exerting a
    certain partial pressure pw ? the partial
    pressure p of the other gases are reduced ?
  • p p . (P pw)/P

39
INFLUENCE OF TEMPERATURE ON SOLUBILITY
  • Gases dissolved in water ? accompanied by
    liberation of heat ?H
  • Le Chatelier principle ? increase of temperature
    results in a decrease of solubility ? vant
    Hoffs equation
  • d(ln kD)/dT ?H/(RT2)
  • where R universal gas constant
  • T absolute temperature K
  • ?H change of heat content
    accompanying by the absorp- tion of 1 mole
    of gas (J/mole)

40
INFLUENCE OF TEMPERATURE ON SOLUBILITY
  • By integrating between the limits T1 and T2
  • ln(kD)2/(kD)1 (?H/R)(T2-T1)/(T1.T2)
  • The product T1 .T2 does not change significantly
    within the temperature range encountered in gas
    transfer operations
  • (kD)2 (kD)1. econst (T2 T1)

41
INFLUENCE OF IMPURITIES ON SOLUBILITY
  • Other constituent that may be contained in water
    influence the solubility of gases ? expressed by
    an activity coefficient ?
  • cs (kD/?).cg
  • For pure water ? 1
  • ? ? generally increases as the concentration of
    substances dissolved in water rises ? lowering
    the solubility

42
INFLUENCE OF IMPURITIES ON SOLUBILITY
  • The influence of concentration of impurities cimp
    on the activity coefficient
  • for non-electrolytes
  • log ? f . Cimp
  • for electrolytes
  • log ? f . I
  • where f a constant depending on the matter
    dissolved in water
  • I ionic strength of electrolyte

43
DIFFUSION
  • The phenomenon of diffusion ? the tendency any
    substance the spread uniformly throughout the
    space available to it ? in environmental
    engineering ? diffusion phenomena the liquid
    phase in gas transfer operations

44
DIFFUSION
  • For a quiescent body of water of unlimited depth
    contacting the gas by an area of A ? the rate of
    mass transfer dM/dt as a consequence of diffusion
    of the gas molecules in the liquid phase ? Ficks
    Law
  • (dM/dt) -D.A (dc/dx) (g/s)
  • where
  • D coefficient of molecular diffusion (m2/s)
  • x the distance from the interfacial area A
  • dx/dt concentration gradient

45
DIFFUSION
46
DIFFUSION
47
DIFFUSION
48
DIFFUSION
  • The total amount of gas M (g) that has been
    absorbed through the surface area A during the
    time t ? independent of x ?
  • under conditions of unlimited depth of water body

49
DIFFUSION
  • If the depth is not too small ? the time of
    diffusion is not too long ? diffusion is very
    slow process and only very little gas is brought
    into deeper layers of the water body

50
THE CONCEPT OF GAS TRANSFER COEFFICIENTS
51
THE CONCEPT OF GAS TRANSFER COEFFICIENTS
  • In accordance with Ficks Law ? the mass
    transport per unit time (g/s) is proportional to
    the concentration difference
  • for the gas phase
  • for the liquid phase

52
THE CONCEPT OF GAS TRANSFER COEFFICIENTS
  • where
  • kg partial gas transfer coefficient for
    the gas phase
  • kL partial gas transfer coefficient for
    the liquid phase
  • cgi and cLi ? generally not known ?
  • cLi kD . cgi
  • ?

53
THE CONCEPT OF GAS TRANSFER COEFFICIENTS
  • The total gas transfer coefficient KL is composed
    of both the partial coefficients and the
    distribution coefficient
  • then
  • m A KL (kDcg cL)

54
THE CONCEPT OF GAS TRANSFER COEFFICIENTS
  • The value of kD/kg will be very small with
    respect to 1/kL ? the influence of the gas
    transfer coefficient of the gas phase may be
    neglected ?
  • KL kL
  • and consequently
  • m A kL (kDcg cL)

55
FILM THEORY
56
FILM THEORY
57
FILM THEORY
58
FILM THEORY
59
FILM THEORY
60
PENETRATION THEORY
  • During the time of exposure the gas diffuses into
    the fluid element ? penetrates into liquid.
  • In contrast to the film theory, the penetration
    process is described by unsteady diffusion

61
PENETRATION THEORY
62
PENETRATION THEORY
63
PENETRATION THEORY
  • During the time of the liquid the interface to
    the gas, the gases penetrate into the liquid at a
    diminishing rate. The total mass of gas absorbed
    during this time

64
PENETRATION THEORY
  • Hence the average absorption rate m (g/s) during
    the time t is defined by
  • The penetration assumes
  • t tc
  • for a gas transfer process operated under
    steady state condition

65
PENETRATION THEORY
  • The final form of the rate expression for gas
    absorption as proposed by the penetration theory

66
PENETRATION THEORY
  • According to the penetration theory
  • stating that the coefficient of gas transfer is
    proportional to the root of the coefficient
    diffusion.

67
PENETRATION THEORY
  • Assumption of a constant time of exposure of
    fluid elements to the gas phase ? a constant rate
    rc (s-1)
  • Taking rc instead of tc

68
SURFACE RENEWAL THEORY
  • The model underlying the surface renewal theory
    is equal to that of the penetration theory ?
    unsteady diffusion of the gas into liquid
    elements exposed to the gas phase.
  • However, this theory does not assume that the
    time to be constant ? follow a frequency
    distribution f(t) with ages of the fluid elements
    ( time of exposure) ranging from zero to
    infinity.

69
SURFACE RENEWAL THEORY
  • The theory is based on the assumption ? the
    fraction of the surface having ages between t and
    tdt is given by
  • ? if the surface element of any age always has
    chance of s.dt of being replaced ? if each
    surface element is being renewed with a frequency
    s, independent of its age

70
SURFACE RENEWAL THEORY
  • The average rate of gas transfer is
  • The surface renewal theory forecasts

71
FILM-SURFACE-RENEWAL THEORY
  • This theory attempts a combination of the film
    theory and the surface renewal theory in
    principle ? a combination of steady and unsteady
    diffusion.
  • The gas transfer coefficient as a function of the
    rate of surface renewal s and max x dL

72
COMPARISON OF THE THEORIES
73
FACTORS AFFECTING THE GAS TRANSFER COEFFICIENTS
  • The effects of temperature on the rate gas
    transfer (effects on kL and A)
  • The temperature coefficient ? for oxygenation of
    sewage ? in the range of 1,016 to 1,047.

74
FACTORS AFFECTING THE GAS TRANSFER COEFFICIENTS
  • The influence of hydrophobic constituents and
    surface active agents on the rate of gas transfer
    ? Gibbs adsorption equation
  • c concentration of hydrophobic substance in
    the bulk of the solution (g/m3)
  • S excess concentration of hydrophobic
    substance at the surface (g/m3) as compared with
    that of the bulk solution
  • R universal gas constant
  • d?/dc rate of increase of surface tension with
    increasing the concentration of the
    hydrophobic substance

75
FACTORS AFFECTING THE GAS TRANSFER COEFFICIENTS
76
FACTORS AFFECTING THE GAS TRANSFER COEFFICIENTS
77
THE OVERALL GAS TRANSFER COEFFICIENT OR AERATION
COEFFICIENT
  • Under steady state conditions of gas transfer
    operation ? the coefficient diffusion and the
    time of exposure may be assumed constant
  • where k2 or kL.a is the overall gas transfer
    coefficient.

78
THE OVERALL GAS TRANSFER COEFFICIENT OR AERATION
COEFFICIENT
  • The rate of gas transfer can be expressed as the
    rate of concentration change
  • which integrates with c0 at t0 to
  • or

79
THE OVERALL GAS TRANSFER COEFFICIENT OR AERATION
COEFFICIENT
  • The overall gas transfer coefficient k2 can
    easily determined experimentally by measuring the
    change of concentration as a function of time and
    by plotting log (cs-c)/(cs-c0) versus time

80
THE EFFICIENCY COEFFICIENT
  • With some transfer operations, e.g. cascades,
    weir aeration ? difficult or impossible to
    determine the parameter time t.
  • If now a constant time tk is assumed for the
    aeration step under steady state conditions

81
THE EFFICIENCY COEFFICIENT
82
THE EFFICIENCY COEFFICIENT
83
THE OXYGENATION CAPACITY
84
THE OXYGENATION CAPACITY
85
THE OXYGENATION CAPACITY
86
AIR STRIPPING
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AIR STRIPPING
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