Page 276 - Fundamentals of Water Treatment Unit Processes : Physical, Chemical, and Biological
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Coagulation                                                                                      231



            Dielectric coefficient: The field between a pair of oppositely  Electron volt: Work done to an electron in moving it
                   charged parallel plates and the induced charges on  through an electric field under a potential differ-
                   the surfaces of a dielectric adjacent to the plates.  ence of 1 V. 1.0 eV ¼ 1.60217733   10  19  C; also,
                   An insulator, or dielectric, is a substance within  1.0 eV ¼ 1.6022   10  19  J. [C ¼ 1.0 A   1.0 s]
                   which there are a few or no charged particles free  Electrophoresis: The movement of a charged particle in an
                   to move under the influence of an electric field.    electric field. A charged particle moves toward a
                   Representative values of the coefficient, D, are    plate of opposite charge at a velocity proportional
                   D(vacuum) ¼ 1,  D(glass) ¼ 5–10,  D(rubber) ¼      to the potential gradient in V=cm.
                   2.5–35, D(water) ¼ 81, D(air) ¼ 1.00059 (Sears,  Electrophoretic mobility (EM): The electrophoretic mobil-
                   1947, p. 177). See also permittivity.              ity, EM, is the particle velocity per unit of field
            Diffuse layer: Ion cloud of counterions having charge oppos-  strength with SI units, m=s=V=m (Pilipovich et al.,
                   ite the surface charge of the colloid; also called the  1958, p. 1469; Gregory, 1975, p. 65, 67).
                   ‘‘Gouy’’ layer.                             Emulsion: Suspension of one liquid in another, for example,
            Disinfection by-product (DBP): Products formed due to     globules of fat in water (Saville, 1917, p. 80).
                   the reaction between a disinfectant and organic  Enhanced coagulation: The addition of alum (or ferric ion)
                   carbon.                                            in excess of that required for removal of colloidal
            Dispersed phase: Two disperse phases important in water   particles to the extent that a substantial amount of
                   systems include a gas in a liquid and particles in  NOM is also removed. The term has been around
                   water (Stumm and O’Melia, 1968, p. 532; Myers,     since about 1984 in general usage, being introduced
                   1991, p. 191).                                     by Kavanaugh (1978) as ‘‘modified’’ coagulation.
            Dispersion: A colloidal dispersion is the solid and liquid  Enhanced coagulation end point: Dosage of coagulant
                   phases together. A system of fine particles is called  and=or pH value which, when achieved, no longer
                   a colloidal dispersion, or a sol (Sennett and Olivier,  produces significant TOC reduction (Pizzi and
                   1965, p. 33).                                      Rodgers, 2000, p. 4).
            Dispersion forces: The same as London-van der Waals  Equilibrium: As pertaining to a chemical reaction, the prod-
                   forces and sometimes called dispersion forces      ucts and reactants have concentrations that do not
                   because the electron oscillations involved are also  change with time.
                   responsible for the dispersion of light; the term is  Equilibrium constant: The ratio of product concentrations in
                   distinguished from dispersions of particles (Gregory,  mol=L to reactant concentrations in mol=L, the stoi-
                   2006, p. 67).                                      chiometric coefficients are exponents. The equilib-
            Dissolved organic carbon (DOC): Organic carbon passing    rium constant is designated, K a . The negative log of
                   through a 0.45 mm filter (Randtke, 1988, p. 43).    K a is designated, pK a , that is,  log K a ¼ pK a .As an
            DLVO theory: A theory of colloid stability synthesized by  example of the use of pK a , for carbonate equilibria,
                   four investigators in colloid science, Derjaguin–  HCO 3    is predominant in the range, 4.35 < pH <
                   Landau–Verwey–Overbeek that integrates electrical  10.33, which are the respective pK a that separate
                   repulsion between particles with van der Waals     HCO 3 from H 2 CO 3 and CO 3 , respectively.
                                                                                               2

                   attraction.                                 Equilibrium diagram: A diagram that delineates equilib-
            Double layer: A negatively charged colloid in water has   rium concentration relationships between a pair of
                   both a ‘‘fixed layer’’ of positive ions bound to the  species in a chemical reaction.
                   particle (as described by Helmholz and Stern) and an  Faraday: Amount of electric charge required to liberate 1 g
                   ‘‘ion cloud’’ that emanates from the fixed layer (as  equivalent of material at an electrolytic cell
                   described by Gouy and Chapman). These two          1 Faraday ¼ 96,514 C
                   parts, the fixed layer and the ion cloud, were termed  Ferric iron salt: The ferric salts used in water treatment
                   the ‘‘double layer.’’ The diffuse layer is characterized  include FeCl 3 and Fe 2 (SO 4 ) 3 ; usually, they are
                   by a gradual change in potential, due to the       hydrated with 6 and 4.5 waters, respectively.
                   thermal energy of the ions (Sennett and Olivier,  Floc: An aggregation of microflocs induced usually by
                   1965, p. 36).                                      hydraulic turbulence causing a growth in size such
            Electric field: A potential gradient. Also, a charged particle at  that settling occurs readily. Size may range 0.1–5mm.
                   a point, A, causes an electric field (Sears, 1947,  Flocculation: Flocculation is the physical process of bringing
                   p. 17).                                            the coagulated particles into contact to promote floc
            Electrokinetic: When two phases exist, that is, a solid and a  formation. The term, flocculation comes from the
                   liquid, each surface is likely to have a charge. When  Latin word, flocculus—a small tuft of wool or a
                   one phase moves past the second phase, four effects  loosely fibrous structure (Black, 1967, p. 277).
                   are possible, depending on the way the motion is  Flocculent: A chemical added to produce growth in size of
                   induced: (1) electrophoresis, (2) electroosmosis, (3)  destabilized particles or precipitate. Usually floccu-
                   streaming potential, (4) sedimentation potential   lents are commercial polymers introduced into the
                   (Hunter, 1981, p. 2).                              flow prior to mechanical flocculation.
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