SciELO - Scientific Electronic Library Online

 
vol.23The solar chimney air standard thermodynamic cycle author indexsubject indexarticles search
Home Pagealphabetic serial listing  

Services on Demand

Journal

Article

Indicators

    Related links

    • On index processCited by Google
    • On index processSimilars in Google

    Share


    R&D Journal

    On-line version ISSN 2309-8988Print version ISSN 0257-9669

    R&D j. (Matieland, Online) vol.23  Stellenbosch, Cape Town  2007

     

    Evaporation from a Water Surface: Theory and Experiment

     

     

    D.G. KrögerI; G.R. BranfieldII

    IProfessor Emeritus. Department of Mechanical and Mechatronic Engineering. University of Stellenbosch Private Bag X1. 7602 Matieland. E-mail: dgk@sun.ac.za
    IIPost-graduate student. Department of Mechanical and Mechatronic Engineering. University of Stellenbosch. Private Bag X1. 7602 Matieland

     

     


    ABSTRACT

    Evaporation from a horizontal water surface that is exposed to the natural environment is analysed. An approximate equation is deduced that predicts the turbulent convection mass transfer or evaporation rate for cases where the water surface temperature is measurably higher than that of the ambient air. An empirical equation is recommended in the case where the temperature difference is relatively small and for application at night. Evaporation rates are measured and the results are found to be in good agreement with predicted values.

    Additional keywords: Mass transfer


     

     

    Nomenclature

    Roman

    cMolar concentration of species [mol/m3]

    CfFriction coefficient

    cpSpecific heat [J/kg K]

    DDiffusion coefficient [m2/s]

    gGravitational acceleration [m/s2]

    kThermal conductivity [W/m K]

    hHeat transfer coefficient [W/m2 K]

    I Solar irradiation [W/m2]

    mMass flux [kg/sm2]

    pPressure [N/m2]

    qHeat flux [W/m2]

    TTemperature [°C or K]

    tTime [s]

    v Speed [m/s]

    wHumidity ratio [kg vapour/kg dry air]

    z Coordinate

    Dimensionless numbers

    Le Lewis number, k/(ρcpD)

    Pr Prandtl number, μcp/k

    Ra Rayleigh number,

    Sc Schmidt number, μ/(ρD)

    Greek

    αThermal diffusivity, k/(ρcp)9 [m2/s] or solar absorptivity

    δ Concentration or partial density layer thickness, [m]

    θZZenith angle, [°]

    μ Dynamic viscosity, [kg/ms]

    ρ Density, [kg/m3]

    φRelative humidity

    Subscripts

    aAir

    avAir-vapour mixture

    aviAir-vapour mixture at initial condition

    avoAir-vapour mixture at z = 0

    cConcentration

    DMass diffusion

    enEnergy

    expExperimental

    hHorizontal

    i Initial condition

    mUniform mass flux

    oAt z = 0

    qUniform heat flux

    TTemperature

    tTime

    uUnstable condition

    v Vapour

    wWater or wind

    z Zenith

     

    1. Introduction

    In 1802 Dalton's classical paper entitled "Experimental essays on the constitution of mixed gases; on the force of steam or vapour from water and other liquids at different temperatures, both in a Torricellian vacuum and in air; on evaporation and on the expansion of gas by heat", was published. In this paper Dalton stated that the rate of evaporation from a water surface is proportional to the difference in vapour pressure at the surface of the water and that in the surrounding air, and furthermore that the wind speed affects this proportionality1. Subsequently numerous researchers investigated the problem of evaporation on the basis of Dalton's model. A recent critical and comprehensive review of many of the empirical equations employed to predict evaporation rates from water surfaces is presented by Sartori2. Other references are listed by Bansal and Xi3 and Tang et al.4. It follows from these publications that there was essentially no further more detailed theoretical modelling of the process of evaporation of water from a horizontal surface into the natural environment subsequent to Dalton's publication. Much uncertainty exists and significant discrepancies occur between empirical equations that predict rates of evaporation under different conditions.

     

    2. Analysis

    In the following analysis an approximate equation is deduced that predicts the convective mass transfer or evaporation rate per unit area from a horizontal water surface exposed to the natural environment. Initially the transfer rate due to natural convection only is deduced and the equation is then extended to make provision for windy (forced convection) conditions.

    Consider a stationary semi-infinite fluid (binary mixture consisting of air and water vapour) in which the concentration cvi of the species of interest (water vapour) is initially uniform.

    Beginning with the time t = 0, the concentration at the z = 0 boundary or surface is maintained at a greater level cvo as shown in figure 1(a).

     

     

    Water vapour will diffuse into the semi-infinite medium to form a concentration boundary layer, the thickness of which increases with time.

    The mathematical equation of time dependent diffusion in a binary mixture, expressed in terms of the molar concentration c is as follows:

    The diffusion flux is driven solely by the concentration gradient strictly in an isothermal and isobaric medium. Nevertheless, equation 1 is a good approximation in many non-isothermal systems, where temperature differences are relatively small. If changes in Kelvin temperature are small the diffusion coefficient D can be assumed to be constant.

    Equation 1 is analogous to the time-dependent equation for heat conduction into a semi-infinite solid body i.e.

    If the temperature of a semi-infinite solid is initially uniform at Ti and a sudden increase in temperature to To occurs at z = 0 as shown in figure 1(b), Schneider5 shows that the temperature gradient at z = 0 is given by

    An effective heat transfer coefficient can be expressed in terms of this heat flux i.e.

    Similarly, by solving equation 2 for the case where the semi-infinite solid at an initial uniform temperature Ti is suddenly exposed to a constant surface heat flux qq, the latter can, according to Holman6, be expressed in terms of an effective surface temperature Toq as

    Although equation 2 is applicable to a solid, it is a good approximation when applied to a thin layer of gas or vapour near a solid surface.

    Due to the analogy between mass and heat transfer the solution of equation 1 gives the following relations corresponding to equations 3 to 8 respectively:

    If the initial concentration at z = 0 is suddenly increased to

    If vapour is generated uniformly at a rate mvm at z = 0, this mass flux can be expressed in terms of an effective concentration cvom to give analogous to equation 6

    These latter equations are applicable in the region of early developing concentration distribution in a semi-infinite region of air exposed to a water or wet surface. According to Merker7 for a Rayleigh number Ra > 1101, unstable conditions prevail with the result that water vapour is transported upwards away from the wetted surface by means of "thermals"as shown in figure 2.

     

     

    The generation of such thermals is periodic in time, and both spatial frequency and rate of production are found to increase with an increase in heating rate.

    For an analysis of the initial developing vapour concentration distribution near the suddenly wetted surface at z = 0, consider figure 1(a).

    The approximate magnitude of the curvature of the concentration profile is the same as the change in slope dcv /z across the relatively small concentration layer thickness or height δD i.e.

    The approximate magnitude of the term on the right-hand side of equation 1 can be deduced by arguing that the average concentration of the δD-thick region increases from the initial value cvi by a value of (cvo - cvi)/2 during the time interval of length t.

    It is stressed that these equations are only applicable to the first phase of the heat or mass transfer process (growth of concentration layer) and do not include the second phase during which thermals exist (breakdown of concentration layer). No simple analytical approach is possible during this latter phase, although the mean mass transfer coefficient during the breakdown of the concentration layer will probably not differ much from the first phase. This would mean that the mean mass transfer coefficient over the cycle of conduction or concentration layer growth and breakdown is of approximately the same value as that obtained during the first phase of the cycle.

    By following a procedure similar to the above, the analogous problem of heat transfer during natural convection above a heated horizontal surface for a constant surface temperature of To can be analysed to find according to Kröger8

    Note the similarity between equations 23, 24, 25 and 26 respectively. These equations are applicable to natural convection mass and heat transfer respectively.

    In the absence of winds, effective values of in equations 23 and 24 and ρi in equation 25 and 26 respectively, change with time (t > tu).

    During windy periods (forced convection) evaporation rates generally increase with increasing wind speed. According to the Reynolds-Colburn analogy and the analogy between mass and heat transfer, the following relations exist6

    In general the rate of mass transfer or evaporation from a horizontal wetted surface at a uniform concentration cvo is thus

    For relatively small temperature differences, the concentrations in equation 29 can be replaced by the partial vapour pressures i.e. c=pv/RvToi where Toi = (To + Toi)/2and Rv =461.52 J/KgK. Furthermore, for air-water vapour mixtures Sc 0.6.

    Substitute these values into equation 29 and find

    Similarly, if the vapour is generated uniformly at z=0 find the rate of evaporation according to equations 24, 27 and 28 i.e.

    Since the thermal conductivity of water is not negligible, it is not possible to achieve a truly uniform heat flux situation. The value of the dimensionless mass transfer coefficient as given by equation 24 may thus be less than 0.243, i.e. it will be some value between 0.243 and 0.155 as given by equation 23. Burger and Kröger9 report the results of experiments conducted during analogous heat transfer tests between a low thermal conductivity horizontal surface and the environment. They obtain a value of 0.2106 instead of the theoretical value of 0.243 given in equation 26 and the analogous equation 24. They furthermore obtain a value of Cf= 0.0052 based on a wind speed measured 1 m above the test surface. With these values equation 26 applied over a wetted surface can be extended to become

    When density differences are very small and conditions near the surface are relatively stable or at night when Toq < Ti and the heat flux is uniform they recommend

    In cases where Toq < Ti and hq according to equation 33 is larger than the value of hq obtained according to equation 32, the former is applicable. If the above values (0.2106 and Cf= 0.0052) are substituted into equation 31 find

    Equation 37 is found to be in good agreement with equations recommended by Tang et al.4. This expression is applicable at night and during the day when the value for mvom is found to be larger that that given by equation 34.

    The density of the ambient air is given by

    Sartori2 lists many empirical correlations that predict the rate of evaporation. The values given by these equations may differ significantly over a range as shown by the shaded area in figure 3. In part this may be due to errors in the determination of the water surface temperature, as well as different vapour concentration distributions above water surfaces having different areas. In figure 3 the rate of evaporation is shown as a function of wetted surface temperature To and ambient air temperatures Ti= To - 5, a relative humidity of φ = 45 per cent and a wind speed of vw = 3 m/s at about 1m above the wetted surface. Sartori2 recommends the equations proposed by the WMO10 and McMillan11 as shown in figure 3. Equation 34 is also shown in figure 3 for an ambient pressure of p = 105 N/m2.

     

     

    3. Experimental Apparatus and Procedure

    To experimentally determine the rate of evaporation from a water surface exposed to the natural environment, the use of an evaporation pan as shown in figure 4 was employed. It consisted of a 50 mm thick horizontal polystyrene plate having an effective upper surface area of approximately 0.97 m2, which was painted with a waterproof matt black paint. A 3 mm high bead of silicon sealant was run along the perimeter of the pan, with the purpose of containing a 1 - 2 mm deep layer of water. Five type-T thermocouples were embedded flush in the surface of the plate with the purpose of measuring the water temperature. Four of the five were positioned in the corners of the pan, 150 mm from adjacent sides, while the fifth was placed in the centre. The pan was surrounded by a dry stony surface.

     

     

    The wind speed, ambient air- and dew-point temperatures were measured with the aid of a weather station at a height of 1 m above the ground8. A Kipp and Zonen pyranometer was used to measure the total incident solar radiation on the surface, while diffuse solar radiation readings were measured by shielding the pyranometer from direct sunlight for a period long enough for stable measurements to be taken. All tests were conducted on clear sunny days.

    The evaporation rate from the water surface was measured by adding consecutive quantities of water (500 ml) to the evaporation pan at a temperature similar to that of the remaining water, and recording the period of time taken for each to evaporate. With the average temperature of the water known during the particular period, the mass flowrate or evaporation rate could be determined. This evaporation rate will be denoted by mexp.

    By applying an energy balance to the surface of a film of water on an insulated base that is exposed to the natural environment as shown schematically in figure 4, it is possible to obtain an expression for the rate of evaporation per unit surface area i.e.

    where Ihαw represents the solar radiation absorbed by the surface, εwσ(Toq4- Tsky4) is the sky radiation while hq(Toq- Ti) is the convective heat transfer rate. The absorptivity of solar radiation at the surface of the water is given by Holman6 and can be approximated by the following equation

    where θZ is the zenith angle measured in degrees.

    The surface emits radiation to a sky temperature Tsky, which can be calculated according to

    Berdahl and Fromberg12 express the emissivity of the sky εsky during the day as

    where Tdp is the dew-point temperature measured in degrees Celsius.

    The heat transfer coefficient hq is given by equation 32 while equation 33 is applicable when Toq > T¡ or when the value of hq according to equation 33 during the day is larger than the value obtained according to equation 32. The heat transfer through the polystyrene plate is negligible.

    According to Holman6 the intensity of solar radiation in clear water at a distance z from the surface is given by

    An analysis was performed on equation 34 to determine the sensitivity of the expression to an error of ±1°C in measured water temperature. It was found that equation 34 is very sensitive to water temperature early in the morning and towards evening, while a difference in the predicted evaporation rate of approximately 10% was found during the day. These findings suggest that extreme care should be taken when measuring the water surface temperature Toq.

    Tests were conducted on the 13th and 14th of April 2005 at the University of Stellenbosch Solar Energy Laboratory (33.93° S, 18.85° E), at an altitude of 100 m above sea level with an ambient pressure of 100990 Pa. The associated weather data is given in figures 5 and 6 and the results are shown in figures 7 and 8.

     

     

     

     

     

     

     

     

    Figure 7 shows a comparison between the experimental and theoretical evaporation rates between approximately 8 h and 15 h (14th April). Note that no wind was present until roughly 10 h; figure 7 shows almost 'stunted' evaporation rates until this point which may be due to the accumulation of moist air above the water surface, which lead to an increase in ρvi and thus reduced evaporation. Figure 8 shows evaporation rates over a period of 24 hours. Note that a negative evaporation rate, or condensation in the form of dew is found to occur during the night when the water surface temperature Toq is less than the dew-point temperature Tdp.

    Table 1 compares the experimentally measured quantity of water evaporated between 8.319 h and 14.752 h, with the values predicted by equations 34 and 45. The error margin is calculated with respect to the experimentally measured quantity.

     

     

    Results from above show that equation 34 predicts the measured evaporation rate most accurately, while equation 45 is also within reasonable accuracy.

    Both equations predict condensation on the water surface during night-time operation, while the magnitudes of the predicted rates seem to be of the same order.

     

    4. Conclusion

    Horizontal natural water or wetted surfaces (surface area of approximately one square metre) having a relatively low thermal conductivity and exposed to solar radiation, transfer both mass and heat to the natural environment. Under these conditions the rate of evaporation at the wetted surface will be determined primarily by the heat flux due to solar radiation and can thus be evaluated according to equation 34 for cases where ρavi > ρavo, the free stream vapour concentration cvi is uniform and the wind speed is less than 4 m/s at a height of 1 m above the surface8. Although equation 34 is an approximation it is based on a sound theoretical approach. Equation 37 is recommended for use during the night-time and when it gives a value of mvom that is larger than that given by equation 34.

     

    References

    1. Dalton J, Experimental essays on the constitution of mixed gases on the force of steam or vapour from water and other liquids at different temperatures both in a Torricellian vacuum and in air; on evaporation and on the expansion of gases by heat, Memoirs and Proceedings of the Manchester Literary and Philosophical Society 1802, 5(11), 5-11.         [ Links ]

    2. Sartori, E, A critical review on equations employed for the calculation of the evaporation rate from free water surfaces, Solar Energy, 2000, 68(1), 77-89.         [ Links ]

    3. Bansal PK and XG, Aunified empirical correlation for evaporation of water at low air velocities, International Communications in Heat Transfer, 1998, 25(2), 183- 190.         [ Links ]

    4. Tang Y, Etzion I A and Meir IA, Estimates of clear night sky emissivity in the Negev Highlands, Israel, Energy Conversion and Management, 2004, 45, 1831 - 1843.         [ Links ]

    5. Schneider PJ, Conduction Heat Transfer, Addison-Wesley, Reading, Massachusetts, 1955.

    6. Holman JP, Heat Transfer, McGraw Hill, New York, 1986.

    7. Merker GP, Konvektiewe Wärmeübertragung, Springer-Verlag, Berlin, 1987.

    8. Kröger DG, Convection heat transfer between a horizontal surface and the natural environment, R&D Journal of the South African Institution of Mechanical Engineering, November 2002, 18(3), 49-53.         [ Links ]

    9. Burger M and Kröger DG, Experimental convection heat transfer coefficient between a horizontal surface and the natural environment, (submitted for publication).

    10. WMO-World Meteorological Organization, Measurement and estimation of evaporation and evapotranspiration, In Technical Report, 83, Working Group on Evaporation Measurement, Geneva, 1966, 92.

    11. McMillan W, Heat dispersal - Lake Trawsfynyd cooling studies, Symposium on Freshwater Biology and Electrical Power Generation, Part 1, 1971, 41 -80.

    12. Berdahl P and Fromberg R, The thermal radiance of clear skies, Solar Energy, 1982, 32(5), 299-314.         [ Links ]

     

     

    Received 1 February 2007
    Revised form 26 September 2007
    Accepted 8 October 2007