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Гидрогеология Загрязнений и их Транспорт в Окружающей Среде Yoram Eckstein, Ph.D. Fulbright Professor 2013/2014 Tomsk Polytechnic University Tomsk, Russian Federation Fall Semester 2013 Transport and Fate of Contaminants in Surface Waters Nature of surface waters Free surface in equilibrium with the atmosphere Open system; exchange with the atmosphere, biosphere and the lithosphere Stratification Flow velocity from 0 to x Sources of contaminants Point sources Non-point sources Transport in streams and rivers Manning’s velocity The Manning formula is also known as the Gauckler– Manning formula, or Gauckler–Manning–Strickler formula in Europe. In the United States, in practice, it is very frequently called simply Manning's Equation. The Manning formula is an empirical formula estimating the average velocity of a liquid flowing in a conduit that does not completely enclose the liquid, i.e., open channel flow. All flow in so-called open channels is driven by gravity. It was first presented by the French engineer Philippe Gauckler in 1867, and later re-developed by the Irish engineer Robert Manning in 1890. Transport in streams and rivers Manning’s velocity 𝑘 𝑣= 𝑛 2 3 𝑅ℎ 1 𝑆2 𝑣 is the cross-sectional average velocity (L/T; ft/s, m/s); k is a conversion factor of (L1/3/T), 1 m1/3/s for SI, or 1.4859 ft1/3/s U.S. customary units, if required. n is the Gauckler–Manning coefficient, it is unitless; Rh is the hydraulic radius (L; ft, m); dx S = the slope of the water surface or the linear hydraulic dl head loss (L/L) (S = hf/L). Transport in streams and rivers Manning’s velocity – hydraulic radius 𝐴 𝑅ℎ = 𝑃 Rh is the hydraulic radius (L); A is the cross sectional area of flow (L2); P is the wetted perimeter (L). The hydraulic radius is a measure of a channel flow efficiency. Flow speed along the channel depends on its cross-sectional shape (among other factors), and the hydraulic radius is a characterization of the channel that intends to capture such efficiency. Transport in streams and rivers Manning’s velocity 𝑘 𝑣= 𝑛 2 3 𝑅ℎ 1 𝑆2 n - the Gauckler–Manning coefficient 1 𝑑506 𝑛= 21.2 where d50 = median sediment diameter, m. The Gauckler-Manning roughness coefficient 0.012 < n < 0.050 smooth rough concrete mountain bed streambed Transport in streams and rivers Chezy’s velocity v - velocity dx v C R dl C – Chezy friction coefficient dx - hydraulic gradient dl Transport in streams and rivers dx v C R dl Chezy friction coefficient 1 1/6 𝐶 = (𝑅ℎ ) 𝑛 Travel time l - length x2 l 1 t dx v x1 v x v - velocity Q = v∙A Ji = Q∙Ci Rate of flow (l3/t) flux of a chemical (M/t) Miscible conservative tracer D – dispersion coefficient Miscible conservative tracer Gaussian (normal) curve – longitudinal D 1 C( x) e 2 x2 2 2 D 2 2t where σ is the standard deviation and C(x) is concentration of the transported chemical Miscible conservative tracer Gaussian (normal) curve – longitudinal D 1 C ( x, t ) e 2 D t 2 x2 2 2 Dl t l C ( x, t ) 1 4 D t l e ( x vt )2 4 Dl t Miscible conservative tracer Gaussian normal curve – longitudinal D M C ( x, t ) e 4 D t ( x vt )2 4 Dl t l M – mass of the tracer Miscible non-conservative tracer Gaussian normal curve – longitudinal D M C ( x, t ) e 4 D t ( x vt )2 4 Dl t e kt l M – mass of the tracer M C e 4 D t max l kt Miscible non-conservative tracer Transversal dispersion l l - the length of the transverse mixing zone Miscible non-conservative tracer Gaussian normal curve – transversal D 2D t w t t w – width of the river l - the length of the transverse mixing zone t = l/v wv l 2D 2 t Longitudinal and transversal mixing Longitudinal mixing is dominated by the process of dispersion Transversal mixing is caused only by flow turbulence Turbulence is predominantly by shear velocity: u* = ½ [gd(dx/dl)] where d is the depth of the river Longitudinal and transversal mixing for straight channels: Dt = 0.15 d u* for natural channels: Dt = 0.6 d u* Longitudinal and transversal mixing Dl = (0.011 2 v w – width of the river w )/(d u*) Lakes & estuaries Wind driven advection 2-d mixing Stratification – thermocline - halocline Tidal effects in estuaries Wind driven advection The Lake Erie surface at the east end stands ca. 1 m higher than at the west end Wind driven advection Summer lake stratification Wind driven advection Summer lake stratification Wind driven advection End of summer stratification Wind driven advection Fall mixing Wind driven advection Winter lake stratification Thermocline and halocline January 2010 temperature and salinity profiles in Arctic Ocean Thermocline and halocline Stream transport Dissolved load Suspended load Bed load Solid particles in surface waters Suspended load Bed load Solid particles in surface waters Mineral – metal-hydroxides - clay ρ ≈ 2.6 g/cm3 Organic – bacteria & algae ρ ≈ 1.3 g/cm3 Solid particles in surface waters and air Particle Settling Stokes’ Law 2 g 1 r 9 s f f f Bottom sediments record 2 Particle Settling Stokes’ Law Bottom sediments record Bottom sediments record How do we establish the age of layers in lake sediments record? 210Pb dating is based on a relatively constant atmospheric deposition of this radionuclide onto surface waters and subsequent sorption of 210Pb on particles in the water that eventually settle into a chronostratigraphic deposit. The 210Pb concentration (measured by its radioactivity) at any depth in the sediment is equal to its concentration in freshly deposited material (at the water/sediment interface) is multiplied by exp(-λt), where λ is the 210Pb decay constant = 0.03/year How do we establish the age of layers in lake sediments record? Therefore: −1 𝐴𝑑 𝑡= × ln( ) 𝜆 𝐴𝑜 Where: Ad is 210Pb activity at a depth d Ao is 210Pb activity at lake sediment surface λ = 0.03/year Concentration and Partial Pressure of Gases in Air Partial pressure = Percentage of concentration of specific gas × Total pressure of a gas Dalton’s law Total pressure = Sum of partial pressure of all gases in a mixture Concentration and Partial Pressure of Gases in Air Ambient Air O2 = 20.93% = ~ 159 mm Hg PO2 CO2 = 0.03% = ~ 0.23 mm Hg PCO2 N2 = 79.04% = ~ 600 mm Hg PN2 Air-Water Exchange Cequil = Ca/H J = -kw(Cw – Ca/H) kw is gas exchange coefficient Cw is the gas concentration in water Ca is the gas concentration in air Air-Water Exchange Solubility of CO2 and oxygen in pure water The tragedy at Lake Nyos, Cameroon Lake Nyos is a deep volcanic crater lake, 5,900 feet (1,800 m) across and 682 feet (208 m) deep, that is thermally stratified, with layers of warm, less dense water near the surface floating on the colder, denser water layers near the lake's bottom. Over long periods, carbon dioxide gas seeping from underground lava dissolve into the cold water at the lake's bottom in great amounts. The amount of CO2 entering the lake is estimated to be about 90 million kilogrammes annually. The tragedy at Lake Nyos, Cameroon Lake Nyos fills a roughly circular maar in the Oku Volcanic Field, an explosion crater caused when a lava flow interacted violently with groundwater. The maar is believed to have formed in an eruption about 400 years ago, and is 1,800 m (5,900 ft) across and 208 m (682 ft) deep The tragedy at Nyos Lake, Cameroon Over time, the bottom layers of the lake become supersaturated with CO2. When this occurs, the lake becomes dangerously unstable, and an event such as an earthquake or landslide can trigger a catastrophic outgassing. This was the situation on August 21, 1986. The tragedy at Nyos Lake, Cameroon On August 21, 1986 a small landslide in the lake disturbed the lake stratification triggering outgassing and up to a cubic kilometre of gas was released. Because CO2 is denser than air, the gas flowed down two valleys in a layer tens of metres deep, displacing the air and suffocating all the people and animals. The gas killed all living things within a 15-mile (25km) radius of the lake, suffocating 1,700 people and 3,500 livestock in nearby towns and villages. The tragedy at Nyos Lake, Cameroon The normally blue waters of the lake turned a deep red after the outgassing, due to iron-rich water from the deep rising to the surface and being oxidised by the air. The level of the lake dropped by about a metre, representing the volume of gas released. The solution at Nyos Lake, Cameroon The method consists of a pipe set up vertically between the lake bottom and the surface. A small pump raises the water in the pipe up to a level where it becomes saturated with gas, thus lightening the water column; consequently, the diphasic fluid rises to the surface. Therefore, once it has primed the gas lift, the pump is not needed, since the process is self-powered: above the saturation level, isothermal expansion of gas bubbles drives the flow of the gas-liquid mixture as long as dissolved gas is available for ex-solution and expansion. The solution at Nyos Lake, Cameroon Thin-Film Model Ca Molecular diffusion Csa Air film Csw Water film Cw Molecular diffusion Thin-Film Model Water-side control J = -Dw(Cw – Ca/H)/δw where δw is the thickness of the water film if Ca = 0 J = -DwCw/ δw = -kw Cw Thin-Film Model Air-side control J = -(Da/δa) (CwH - Ca) or J = – (Da - H/δa ) (Cw - Ca /H) where δa is the thickness of the air film Thin-Film Model for H ≈ 0.01 1 C J C H D DH a w w w a a Estimating gas exchange coefficient MW k D k D MW A A B B B A Estimating gas exchange coefficient In absence of a tracer with a known gas exchange coefficient models are constructed empirically for each gas, e.g. the four models for kO2 : K O2 24.94 1 N u * d Thackston & Krenkel, 1969 K O2 K O2 V 1.92 d 0.85 Neglescu & Rojanski, 1969 23.2 V 0.73 K O2 d 1.75 Owens et al., 1964 103 V 0.413 w0.273 d 1.408 Bennet & Rathbun, 1972 Estimating gas exchange coefficient Similarly, gas exchange coefficients for slowly flowing waters, lakes or estuaries are approximated empirically: for slowly flowing or stagnant waters: kw[cm/sec] ≈ 4·10-4 + (4·10-5·u2w10) or ka[cm/sec] ≈ 0.3 + (0.002·uw10) Using gas exchange coefficient The air-water flux density is proportional to the difference between a chemical concentration in water [Cw] and the corresponding equilibrium concentration [CwH]. Therefore: C( x ,t ) Co e k r t Thin-Film of Air Model Above a Slick of NAPL P C MW RT a while δa is the thickness of the stagnant air film above the slick, the velocity of gas transfer (vaporization) is proportional to Da of that gas J Da a Ca Thin-Film of Air Model Above a Slick of NAPL the velocity of gas transfer (vaporization) is also dependent on the size of the slick v= -0.11 -0.67 0.029·uw10·L ·Sc where: uw10 wind velocity 10m above the slick [m/hr] L is the slick diameter [m] Sc is the Schmidt number