S-EPA
                                 United States
                                 Environmental Protection
                                 Agency
                                 Municipal Environmental Research
                                 Laboratory
                                 Cincinnati OH 45268
                                 Research and Development
                                 EPA-600/S2-81-062  July 1981
Project Summary
                                 Chemical  Speciation  of
                                 Flue  Gas  Desulfurization (FGD)
                                 Sludge  Constituents
                                 James Lu
                                   This project studies the problem of
                                 flue gas desulfurization (FGD) sludge
                                 disposal to land. Specifically, the
                                 chemical species of FGO sludge con-
                                 stituents are thermodynamically mod-
                                 eled using the equilibrium constant
                                 approach in an attempt to predict the
                                 constituent concentrations in fresh
                                 and aged FGD wastewater and sludge.
                                 This method involves solving the
                                 stoichiometric  equations of various
                                 chemical species subject to constraints
                                 imposed by the equilibrium constants
                                 as well as mass balance and charge
                                 balance relations. Diagrams  such as
                                 Eh-pH plots, ion-ratio plots, concen-
                                 tration pH figures, and species distri-
                                 bution figures are then used to display
                                 the stability field and speciation re-
                                 sults.
                                   The thermodynamic model used in
                                 this study was verified for suitability
                                 and accuracy by the analytical results
                                 of various FGD sludge samples taken
                                 from the Kansas City Power and Light
                                 (La Cygne plant)'. The model was also
                                 operated over a wide range of opera-
                                 tional and chemical changes to theo-
                                 retically determine their impacts on
                                 the concentration and speciation of
                                 various solid and soluble species. The
                                 impacts of (1) changes in pH and ionic
                                 strength; (2) addition of lime, silicates,
                                 hydrogen  sulfide, and phosphates to
                                 the sludge; (3) variation of chloride,
                                 sulfate, and borate levels; (4) addition
                                 of magnesium to the sorbent; and (5)
                                 sulfite oxidation were all estimated
                                 using the model.
                                   This Project Summary was devel-
                                 oped by EPA's Municipal Environmen-
                                 tal Research Laboratory, Cincinnati,
                                 OH, to announce key findings of the
                                 research project that is fully docu-
                                 mented in a separate report of the
                                 same title (see Project Report ordering
                                 information at back).
                                  Introduction
                                   A conventional environmental impact
                                  assessment of flue gas desulfurization
                                  (FGD) sludge disposal would include
                                  chemical analysis and identification of
                                  the total concentrations of constituents
                                  in the sludge and its leachate. However,
                                  public health effects of FGD waste
                                  disposal depend on which chemical
                                  forms or species of the constituents are
                                  released to surrounding waters and not
                                  necessarily on their total concentration.
                                   Thermodynamic modeling is the only
                                  feasible means to obtain contaminant
                                  species information of FGD sludge. A
                                  thermodynamic model can also be used
                                  to predict migration trends of constit-
                                  uents when FGD wastes age; estimate
                                  final concentrations of constituents in
                                  FGD leachate (aged wastewater) without
                                  conducting expensive field monitoring;
                                  and predict effects of operational and
                                  chemical changes in FGD wastes.
                                   Many available techniques can be
                                  used to construct and interpret a chemi-
                                  cal thermodynamic model. In this study,
                                  the equilibrium constant approach is
                                  used.

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Methodology of Species
Analyses
  Two principal graphical treatments,
Eh-pH plots and the ion-ratio method,
are used to describe the stability fields
of constituents in FGD sludge. The Eh-
pH plot  is used for constituents with
different redox species such as iron,
manganese,  mercury, arsenic,  and
selenium. The ion-ratio method is used
for constituents with only one redox
state or for reactions involving no
electron transfer.
  The speciation model is constructed
by the equilibrium constant approach.
The actual mathematical equilibrium
model involves a series of simultaneous
equations that describe  the various
interactions among components of the
system. Seven general equations are
involved (Table 1). To solve these equa-
tions simultaneously, the information
on metal  and  ligand species, overall
formation constants, solubility products
(and/or  Henry's constants), and activity
coefficients must be compiled from the
literature. A computer solution is neces-
sary, as the expanded equations number
in the hundreds. The resultant nonlinear
equations are  solved  by Newton-
Raphson iteration.
   Because the chemical composition of
FGD sludge can vary over an extremely
wide range, this  study focused on
speciation at the lowest  levels (ionic
strength (I) =0 05) and the highest levels
(I  = 0 8). All possible distributions of
species  are expected to be within this
range.

Speciation  of Solid and
Soluble Chemical Species

Fresh  FGD  Sludge
   Thermodynamic modeling of the fresh
FGD wastewater system can be per-
formed  as if no solid was  formed or
dissolved because (1) the equilibrium
conditions among soluble species can
easily be  reached and (2) the rates of
nucleation and dissolution of the solid
species  are very low. A summary of the
predominant  soluble species  shows
that the major ions (i.e., calcium, mag-
nesium, potassium, and  sodium) and
the manganese species exist as free
ions in fresh FGD wastewaters(Table2).
   Other trace  metals,  however, can be
complexed considerably  in the same
wastewaters. Chloride complexes may
under certain conditions become the
predominant  species for cadmium,
copper,  lead, mercury, and zinc; borate
Table 1.    General Models Used for Speciation Calculation
                                    Mpfi)
                                 fi) • L*(j)
  h    a    b
  III  *M(i)»L(Jk  = 1
j = 1 p = 1 q = 1

  g    c    d
  III  *M(i)uL(j)v  - 1
i = 1 u = 1 v = 1

                    k    I     h
[M(ih] = [Mm   +   I    I    I  m[M(i)mL(j)n}
                  m=1n=1j=1

              h    a    b
            + I    I    I  p[M(i)fUj)q]
             j=1 p=1q=1

              h    c    d
            + 1    I    I  n(M(i)mL(j)n]


                    k    I    g
[L(jh] = (L(j),]   +    I    I    I  n[M(i)mL(j)n]
                  m = 1 n = 1 j = 1
               gab
            +  I    I    I
             i = 1 p = ; q = 1
               g    c    d
            +  I    I    I  [M(i)aL(M
             j= 1 u = ; v = 1
                                                                        12)
                                                                        (3)
                                                                        (4)
                                                                        15)
                                                                        (6)
                                                                        (7)
where:
         [M(i)mL(j)n] = concentration of complex M(i)mL(j)n (in
                     moles/ liter)

             [M(i)t] = free metal ion concentration of ith metal
                     (in moles/ liter)

              [L(j)<\ = free concentration ofjth ligand (in
                     moles/liter)

             [M(i)i] - total concentration of ith metal in the
                     system (in moles/ liter)
          and
          nM(i)uL(j}y = mole fraction of solid or gas species for
                     metal or ligand solids

                  i = metal species

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Table 1.    (continued)

                 j - ligand species

                 g = total number of metals

                 h = total number of ligands

                 k = maximum number of metals Mfi) coordinating
                     ligands L(j)

                  I = maximum number of ligands Lfj) coordinating
                     metal Mfi)

       a, b, c, and d = positive integer showing maximum number
                     of metals or ligands in the solids or gases

                   - overall formation constant of complex
                     M(i)mL(j)n

                 Xx = thermodynamic activity coefficient of soluble
                     species x

                 fi = thermodynamic activity coefficient of solid
                     for gas) species x (in this study, assume fx =* 1)

                 K - solubility products or Henry's constants
complexes may become the predominant
species for copper and  lead; sulfite
complexes may become the predominant
species for cadmium  and iron; and
hydroxide complexes may become the
predominant species for mercury, zinc,
and the trivalent metals such as chromi-
um and iron. In fresh FGD wastewater,
arsenic and selenium exist primarily as
arsenate and selenite species. The pre-
dominance of a  given species  can  be
affected significantly by the pH  level of
the wastewater. The ionic strength (or
more specifically, the soluble levels of
the related ligands) also  plays  an im-
portant role in the speciation of most
constituents:

Aged FGD Sludge
  The speciation of constituents in the
solid and soluble phases  of aged FGD
sludge was computed assuming that
the equilibrium condition among all the
soluble and solid species had been
reached.  Because of the  long contact
period, equilibrium conditions between
solid and liquid phases probably can be
reached in aged FGD wastes. The calcu-
lated results are summarized in Table 3.
  Results show that sulfur dioxide re-
moved from the flue gas reacts to form
CaSO< • 2H20(s) and CaS03 • 1 /2H20(s)
in the FGD sludge. In the  aged sludge,
carbonate solids  may become the pre-
dominant species for cadmium, calcium
(when pH isgreaterthan?), copper, lead
(at pH greater than about 9), manganese
(at pH greater than about 7.5), and zinc
(at high ionic strength and pH around 8).
Hydroxide solids are the predominant
species for chromium, iron, cadmium (at
pH greater  than 9), magnesium (at pH
greater than 9),  manganese (at pH
greater than about 9), and  zinc (at low
ionic strength  and pH  greater than
about  9) in the aged sludge. Arsenic,
mercury, and selenium exist primarily
as elemental metals in the aged sludge.
Aluminum  forms predominantly phos-
phate solids at low pH and  oxide solids
at high pH. In aged sludge, the molybdate
and silicate solids are usually the pre-
dominant species for lead and zinc,
respectively
  The  predominant soluble species of
constituents in aged FGD leachates are
similar to  those found  in  fresh  FGD
wastewater. However, the concentra-
tions of these soluble species are  gen-
erally decreased through aging because
of the  nature of solids found. The pre-
dominant soluble species and their
concentrations for each individual con-
stituent at two different ionic strengths
are shown in Table 3. In most cases, the
predominant species alone will account
for a major portion of the concentration.
Therefore,  knowing the predominant
solid and soluble species, the total
soluble concentration of a constituent in
FGD leachate can be easily calculated
without the aid of the computer.

Model Verification
  The thermodynamic model was  veri-
fied  by checking the model results
against both analytical data and certain
theoretical considerations.
  The  model, in relation to analytical
data, was evaluated by comparing the
known soluble concentrations of con-
stituents in aged FGD wastes to those
predicted by the model. The calculated
results for aluminum, arsenic, boron,
cadmium, cobalt, copper, iron, manga-
nese, mercury, potassium, selenium,
sodium, and zinc either approach or are
very close to the concentration levels
experienced in  the field (Table  4). For
other elements (specifically calcium,
chromium, fluoride, lead, and magne-
sium),  the model was not as effective.
The low levels of calcium predicted are
due primarily to the interaction of calcite
with Ca-COa and  CaSOa complexes in
the model. The high levels of chromium
and  lead calculated  are due  to the
inclusion of hydroxide and carbonate
complexes in the model  For fluoride
and magnesium, the discrepancy may
be caused by certain unsuitable solids
included in the model. The discrepancies
also may be due to (1) errors in the
stability constants and activity coeffi-
cients; (2) effects of other mechanisms
such as adsorption by hydroxide solids
or clay minerals; and (3)  effects of
kinetic constraints.
  According to scientific considerations,
in general, the model results behave in
accordance  with  basic chemical and
thermodynamic  principles, including
the effects  of changing pH, Eh, and
ligand  levels
Effects of FGD System and
Sludge Variables on Chemical
Speciation
  To select a sludge treatment or dis-
posal procedure, observing the possible
beneficial or adverse effects of opera-
tional or chemical changes in a FGD
system on sludge speciation is  useful.
The chemical changes studied here
include those of pH, ionic strength,
chloride concentration, borate concen-
tration, sulfate concentration, and
sulfite oxidation (Table  5).  The  opera-
tional changes were limited  to the
addition  of lime, silicates, hydrogen
sulfide,  phosphates, and magnesium
(Table 6).
  A  change in  pH can influence the
direction of the alteration processes
(dissolution,  precipitation,  adsorption,
or complexation) in any chemical system.
In general, a pH increase in the FGD
sludge system tends to dissolve more

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Table 2.    Predominant Species of Soluble Constituents in Fresh FGD Wastewater

                                                           Predominant Species"
              Ionic
 Constituent  Strength         pH - 5                         pH = 7
                                                                                             pH =
Al


As

Cd


Ca

Cr

Co


Cu


 F

Fe

Pb



Mg

Mn

Hg


 K

Se

Na

Zn
              0.05

              0.8
              0.05
              0.8
              0.05

              0.8
              0.05
              0.8
              0.05
              0.8
              0.05
              0.8
                      AIF2+(34),AI(OH}2+(20),
                      AIF2(17)
                      AIF2(55)
                      H2As04'(98)
                      H2As04-(95)
                      Cd2+(50)CdC03(aq)(40)
                                       AI(OH)idOO)

                                       AIF2(38),AIF3(31>
                                       HAs02'(68)
                                       HAs042~(78)
                                       Cd2+(49),CdCr(40)
                      Ca2+(83)
        Cr(OHr<79)
        Cr(OHf*(65)
        Co2+(69)
        Co2*(40>. CoSO4(aqj(26]
Ca^(89)
Ca2+(71)
Cr(OH)2<85)
Cr(OH)2*(81)
              0.05    Cu2*(54)
0.8
0.05
0.8
0.05
0.8
0.05

0.8

0.05
0.8
0.05
0.8
0.05
0.8

0.05
0.8
0.05
0.8
0.05
0.8
0.05
0.8
                      CuB(OH)4(35), CuCf(26)
                      F(25),SnF*(52)
                      CaF+(40),F~(38)
Co2+(40J, CoSO4aq)(26)

Cu(B(OH)4)2faq)(5J)

CufBfOHMaqMSSi
                      FeS03(97)
                      Pb2+(55)
F~(40).MgF+(44)
Fe(OH)2(100)
Fe(OH)2(84)
                      PbSO*(22),Pbz*(21)
                                                     Pb2+(19)
                                                     Pb(B(OH)A)2!aq)<87)
                      Mn2*(79)
                      HgCI3-(47),HgC/42-(26)
                      HgCI,(aq)(27)
                      IC(97)
                      HSe03'(97)
                      HSe03(97)
                      Na*(95)
                      Na"(95)
                      Zn2+(74)
                      Zn2+(47),ZnCr(34)
                                                     Mn2+(78)
                                                     Mn2+(55)
                                                     HgCI2laq)(62)
                                                     HgCI3-(46),

                                                     K+(97)
                                                     K"(89)
                                                     Se03*-(74)
                                                     SeO32'(74)
                                                     Na+(95)
                                                     Na*(95)
                                                     Zn2+(74)
                               AI(OHU'dOO)

                               AI(OH)4-(100)
                               HAs02'(100)
                               HAs042~(97)
                               CdC03(35),Cd2*(21).
                                 CdCI(OHFf20)
Ca2+(81)
Ca2+(71)
Cr(OH)A'dOO)
Cr(OH)4-(100)
CoCO3(aq)(44).Co^(26)

CoCr<20)
                                                                                                    z+(25).
                                                                                     Cu(B(OH)4)2faq)(100)
MgF+(47),F~(45)
Fe(OH)4'(93)
Fe(OH)2(93)
PbfBfOHJMaqjOS).
                                                                                    Mn2*(54)
                               HgCIOH(aq)(52)

                               IC(98)
                               K*I89)
                               SeO3 (99)
                               Se02-(99)
                               Na+(97)
                               Zn(OH)2faq)(68)
                               Zn(OHMaq)(42).
                               ZnCIOH(aq)(26)
 Note: Values in the parentheses indicate the percent of the total concentration.
 alf one species accounts for less than 50 percent of the total concentration, then more than one species will appear.
elemental constituents such as As°(s),*
Hg°(l), and Se°(s) and to transform some
of the carbonate, phosphate, or other
sol ids into hydroxide solids, thus affecting
the concentration of soluble constituents.
A pH change may also affect the ligand
concentrations and, thereby,  change
the concentration of soluble constituents.
  The overall  effects of pH on total
constituent  concentration depend on

*s = solid
 I = liquid
                                        the solubility constants of the new
                                        solids formed, the new ligand concen-
                                        trations, and the formation constants of
                                        the complexes. For example, a high pH
                                        level can increase total soluble mercury
                                        and selenium and yet decrease most of
                                        the other bivalent trace metals. For
                                        trivalent metals such as chromium and
                                        iron, the minimum soluble constituent
                                        concentrations occur in the neutral pH
                                        region.
                                          Although a change in ionic strength in
                                        the FGD  sludge can affect the stability
                                                                            constants, its effects on the soluble
                                                                            levels of constituents or on the stability
                                                                            fields  of  various solids are  usually
                                                                            negligible if their related ligand  levels
                                                                            are unchanged. The  soluble chloride
                                                                            concentration  of  FGD waste  is a very
                                                                            important factor in determining the total
                                                                            soluble level of cadmium, copper, lead,
                                                                            mercury, and zinc. Variations  in borate
                                                                            concentration have an impact primarily
                                                                            on total soluble copper and lead concen-
                                                                            trations. The soluble sulfate concentra-
                                                                            tion may affect the total soluble calcium,

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 Table 3.    Predominant Species of Constituents in Aged FGD Sludge

                               Predominant Solid Species'
                                           Predominant Soluble Species'
                Ionic
  Constituent    Strength
  pH=7
pH =
pH=7
Al

As

Cd


Ca





Cr

Cu



Fe

Pb


Mg

Mn


Hg

K

Se

Na

Zn


005
0.8
0.05
08
0.05
0.8

0.05


0.8


0.05
08
005

08

005
0.8
005
08

0.05
0.8
0.05
08

0.05
08
005
0.8
005
0.8
005
08
0.05
0.8

AI(H2PO,)(OHUs)
AHHtPOJIOHMs)
As°(s)
As°(s)
CdCOds)
CdCOa/s)

CaSOyl /2H10(s).
CaSO*-2H20(s)

CaS03-H,0(sl.
CaSOt-2H20(s)

Cr(OHMs)
CrfOHMsl
CuiCOdOHkls)

CutCOalOHMsl

Fe(OHMs)
Fe(OHMs)
PbMoOtls)
PbMoOtfsi

b
b
b
	 b

Hg°(D
Hg°(D
	 b
b
Se'fst
Se°(s/
	 b
	 b
b
ZnSiOa/s)

AlfHtPOdtOHMs)
AlfHiPOtMOHMs)
As°(s)
As°(s)
CdCOils)
CdCOJs)

CaSOyl /2H,0(s),
CaSOt-2HzO(sl

CaSOyHiO(s),
CaSOt-2H20/s)

Cr(OHMs)
CrfOHMs)
CuiCOJOHMs)

CutCOJOHMs)

Fe(OHMs)
Fe(OHMs)
PbMoOJs)
PbMoOtls)

b
b
b
	 b

Hg°(1)
Hg°(1)
b
b
Se°fs)
Se°(s)
b
b
ZnSiOifs)
ZnSiOJs)
Zn(OHMs)
AlzOvSH&ls)
AlzOy3HtO(s)
As'fsl
As°(s/
CdfOHMs)
Cd(OHUs).
CdCOJs)
CaCOJsl,
CaS03-1 /2H20(s).
CaS04-2H,0{s)
CaCOz/sl,
CaSOi-1 /2HiO(s).
CaS04-2HiO(sl
Cr(OHUs)
CrlOHMs)
Cu2COJOHMs>

CuiCOJOHMs)

Fe(OH)Js)
FefOHMsl
PbMoOJs)
PbMoOJsl.
PbCOJs)
Mg(OH)^s)
MglOHMs)
MnCOJs)
MnfOH/M,
MnCOifsl
Hg°(D
Hg°ID
b
b
Se°(s)
Se°(s)
b
b
ZnfOHMsl
ZnSiOJsl,
ZnCOifsj
AIF*(6 04)
AlFi (5.051
HaAsO,~(8 03)
HaAsO,~(75J/
Cd**(5.23>
cdcris 121

Ca^fO 211


Ca** 10.25)


Cr/OHf*(4. 13)
Cr(OHk"(5.0)
CuBtOH)t*(15.38)
(16 78)
CuB(OH)S(1499)
(1609)
FetOHk"(7 16)
FeS03(6.98)
Pb2t(5.80)
PbCr(5.67)

Mg**(391)
Mg**(0.95)
Mn**l3 49)
Mn2t(3.56)

HgCUaqX22. 1)
HgCli(19 9)
K*(1.89)
K*(1 87)
HSeO3-(28.6)
HSeO,~(28.6)
Na*(1 36)
Na*(0.83)
Zn**(3.63)
Zn*+(3.84)

AI(OH)Jaq)(6 26)
Al(OHMaq)(6 89)
HAsO '-(11.231
HAsO*~(1087)
C^(6.03)
CdCr<5 13)

Ce2*<0 53)


Ca*(0.32)


Cr(OH>2*(4. 76)
Cr(OHk''(4 72)
CulB(OH)Maq)
(16.9)
CutBIOHMdaq)
(164)
Fe(OHk*(9 16)
Fe(OH)i(9. 12)
PbB(OH)S(5.82)
PbB(OH)t*(5 44)

Mg*(3 92)
Mg**(0.95)
Mn*(3.49)
Mn2*(3.56)

HgCUaqlVO 4)
HgCk'118.2)
ICI1.89)
IC(1.87)
Se03*-(18.2)
Se03"-(182)
Na'd.Se)
Na'(0.83)
Zn2t(3.65)
Zn**(4 06)

AI(OH)3(aq)(5.95)
A/(OHMaq)(5.36i
HAsOt2~(8.82)
HAs02'(10.91)
CdtS03)2*-(7. 72)
CdCIOH(aqK6.07)

Ca2t(2. 19)


Ca2*(2 0)


Cr(OH)t-f4 03)
Cr(OHk'(3.99)
Cu(B(OH)^aq)

CufB(OH)Maq)

Fe(OH)t'(10.07)
Fe(OH)t-(8.96)
Pb(B(OH).l3-(7 14)
PbfBfOHMitS.SSI

Mg2tf4. 16)
Mg2*(1. 13)
MnSO,laq)(4. 10)
Mn2tl4.33)

Hg(OH)daq)(17 9)
HgCIOH(aq)(1 7 0)
IC(1.93)
1C Y; 91)
SeO32~(6. 19)
Se032-(6. 19)
Na '(1.37)
N a* (0.85 )
ZnSOJaq)(5 67)
Zn(OHMaq)(5.9i

 Note. Values in parentheses indicate the -log molar concentration.
 'If one species accounts for less than 50 percent of the total concentration, then more than one species will appear for each condition
 "—indicates that there is no stable solid or that the stable solid is in complex forms (e.g., complex silicates)
magnesium, cadmium, and zinc concen-
trations. In general, if the total soluble
levels of the above-mentioned  ligands
(e.g., chloride, borate, and sulfate) are
known,  the total soluble metal concen-
trations in the aged'FGD leachates can
be approximated without extensive
computation.
  For operational changes, sulfite oxi-
dation may reduce the concentration of
sulfite  complexes and  increase the
concentration of sulfate complexes but
have very little  impact on the  total
soluble  concentration of most  metals.
The  most significant effect of sulfite
oxidation  is the transformation of
CaSO3-1 /2H20(s) to CaS04-2H20(s) or
CaCO3(s), depending on pH levels. This
transformation may affect  the  soluble
levels of arsenic, mercury, and selenium
if the redox potential is  controlled by
sulfate/sulfite species.
  Adding lime to FGD sludge is used in
pozzolanic fixation processes to improve
the engineering properties of dewatered
sludge. The model shows, however that
adding lime may adversely affect con-
stituent solubility. Adding lime may
reduce the total soluble levels of certain
constituents such as arsenic and manga-
nese; however, the total soluble levels
of most other trace toxic metals such as
cadmium, chromium, copper, lead, mercu-
ry, selenium, and zinc, increase in aged
FGD sludge following  lime addition.
This may actually increase the potential
for  environmental damage should the
concentration increase outweigh the
dilution  factor decrease that results
from permeability reduction.
  Adding silicates may reduce the total
soluble aluminum and zinc concentra-
tions, but other elements studied are
virtually unaffected.
          Phosphate addition will  only reduce
        two soluble major  ions (calcium and
        magnesium) while increasing the soluble
        cadmium level. Phosphate itself is also a
        water pollutant, so adding phosphates
        is not recommended for the treatment of
        FGD wastewater.
          The addition of hydrogen sulfide may
        reduce the soluble concentrations  of
        trace metals substantially (Table 6). This
        operational change, however, may not
        be desirable for an FGD system because
        (1) hydrogen sulfide itself is a pollutant,
        and (2) the diffusion of oxygen into the
        sludge, followed by the oxidation process,
        will eventually return the soluble metals
        to their original concentration.
          Magnesium improves the efficiency
        of wet FGD systems; therefore, use  of
        high magnesium reagents could become
        commonplace. The model shows that,  in
        general, adding  magnesium will not

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Table 4.    Validity of the Thermodynamic Model for the Prediction of FGD Sludge
           Speciation*
Constituent
Al
As
B
Cd
Ca
Cr
Co
Cu
F
Fe
Pb
Mg
Mn
Hg
K
Se
Na
Zn
Validity of
Modef
Excellent
Good
Excellent
Excellent
Not applicable
Not applicable
Good
Excellent
Not applicable
Good
Not applicable
Not applicable
Excellent
Excellent
Good
Good
Good
Excellent
Reason for Discrepancy




Form strong CaCOafs) when pH >7
Form strong Cr-OH complexes


Solubility-controlling solid unknown

Form strong Pb-COs and Pb-OH complexes
Solubility-controlling solid unknown






 'Based on comparison of modeling results with Kansas City Power and Light FGD
  sludge analysis.
 ^Excellent means that the migration trends of the constituent follow those predicted by
  the model and that measured levels in the aged leachate are within 30 percent of
  those estimated by the model; Good means that both estimated and calculated levels
  of constituents show the same migration trends when FGD waste ages.

significantly affect the total soluble
levels of most constituents.
  The full report was submitted in
fulfillment of Contract No. 68-03-2471
by SCS  Engineers under the sponsor-
ship of the U.S. Environmental Protec-
tion Agency. This Project Summary was
authored by James  Lu  of Cal Science
Research, Inc. for SCS Engineers.

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Table 5.     Effects of Chemical Changes on the Speciation of Constituents in FGD Sludge
  Constituent
                        pH
                                    Ionic Strength
                                                            Chloride
                                                         Concentration
                                                                                       Borate
                                                                                    Concentration
                                                   Sulfate
                                                Concentration
                                                   Sulfite
                                                  Oxidation
     Al
     As
     Cd
Ca
Cr
Co
Fe
Pb
         Solid: High pH levels
         favor the formation of
         AI^>,-3H,0(s); low pH
         levels favor the for-
         mation of AI(HiPOt)
         (OHMs)
         Soluble: When pH is
         higher than about 6,
         the predominant
         species will change
         from AlFt  to Al3' -OH'
         complexes
         High pH levels tend to
         dissolve As°(s) and
         form arsenate species

         Solid. When pH is
         higher than 10.5,
         CdCOstst may grad-
         ually transform to
                                    Negligible (when re-    Negligible
                                    lated ligand concen-
                                    trations are unchanged)
                      Negligible
Negligible
                                    Negligible
                                    The relative distri-
                                    bution of Cd2* and
                                    Cd-CI complexes can
                                    be altered by ionic
                                    strength changes
             Soluble- High pH
             level can lower the
             total Cd level
             Solid CaCOa/s)         Negligible
             may greatly increase in the
             sludge when pH>7
             Soluble. WhenpH>7
             the total Ca and Ca"
             are reduced signifi-
             cantly

             Solid: Cr(OHJ3ts) is      Negligible
             significant when pH
             ranges from 6 to 9
             Soluble: When pH is
             higher than about 4,
             the predominant species
             will change from Cr3*
             to Cr-OH complexes
             Solid: Negligible        Negligible

             Soluble. WhenpH
             >4. 8, the predominant
             species will change
             from Co2* to Cu-
             B(OH)t complexes

             Solid. Negligible        Negligible

             Soluble: High pH
             levels fpH >8.5) tend
             to increase Fe-OH~
             complexes but reduce
             the total Fe levels
             Solid: When pH <9,      Negligible
             PbMoOtls) is predomi-
             nant. otherwise. PbCOi/sl
             is predominant

             Soluble: At high pH
             levels, Pb-COj may
             increase the total Pb
             levels
Negligible
Can greatly affect
the total soluble
Cd levels when chlo-
ride is higher than
certain levels
                                                      Negligible
Negligible
Negligible
                      Negligible
                                                      Negligible
                      Negligible
WhenpH<4.7.
Cu-CI com-
plexes may become
predominant when
the chloride
level is higher
than 2,000 ppm

Negligible
When the bor-
ate level in-
creases from
5 ppm to 2OO
ppm, the solu-
ble lead level
can be increased
about 2,000
Negligible
Negligible
Cd-S0t complex
may become predom-
inant when Cl~,
SO,2', or OH'
complexes are not
significant
                      When pH > 5. and the
                      sulfate level is
                      higher than about
                      5.000 ppm. the CaSOt
                      fag) species may
                      become predominant
                      Negligible
                                            Negligible
                                                                                                                            Negligible
Negligible, if the
redox potential is
not controlled by
sulfate/suHite species
Will reduce Cd(SOJt~
and increase CdSOt/aq)
levels. However.
effects on total solu-
ble Cd and  Cd solids
are negligible
                      Will convert the sul-
                      fite solid into sulfate
                      or carbonate solids.
                      Will have very little
                      effect, however, on
                      soluble Ca
                      Negligible
                                                                                                  Negligible
                      Negligible
                                                                                                  Negligible
                                                      When pH >7, Pb-
                                                      Cl complexes may
                                                      become predominant
                                                      when the chloride
                                                      level is higher
                                                      than J,500 ppm
                      When the bor-
                      ate level in-
                      creases from
                      5 ppm to 200
                      ppm. the solu-
                      ble lead level
                      can be increased
                      about 10.OOO
                      times
                      Negligible
                      Will transform FeSOS
                      to FefSOti. but the
                      solid phase will remain
                      unchanged
                      Negligible

-------
Table 5.
Mg







Mn







Hg







K






Se





Na





Zn








(continued)
Solid: High pH levels Negligible
(pH >9) favor the for-
mation of Mg(OH)ifs)

Soluble. When pH is
increased, the MgSOt
(aq) species may be-
come significant
No significant effect Negligible
on predominant solu-
ble species. However.
the total soluble level
will be decreased at
high pH levels because
of the formation of
more solid
Low pH levels favor the Negligible
formation of Hg°(1) in
the sludge. High pH
levels tend to increase
the soluble levels of
HgCI,, HgCI*
HglOHkfaq). and
HgCIOHfaql
Slightly reduces the K' Negligible
levels when pH is
increased




High pH levels tend to Negligible
dissolve Se°(sj and
form selenate species



Will slightly reduce Negligible
the Na* levels when
pH increases



Solid: High pH levels Negligible
favor the formation of
Zn(OHMs). When pH
decreases, ZnSiOsfs)
will replace Zn(OHMs>

Soluble: Will reduce
total levels when pH
increases

Negligible Negligible







May affect the Negligible
levels of
Mn-CI com-
plexes, but will
not change the
total soluble
levels signifi-
cantly
When the chloride Negligible
level varies from
50 to 6,OOO ppm, the
total soluble Hg can
be increased for
more than four orders
of magnitude

Negligible Negligible






Negligible Negligible





Negligible Negligible





When pH <9, the Negligible
total soluble Zn
exists predomi-
nantly as ZnCr if
the chloride level
is higher than
3.00O ppm



When the soluble
sulfate level is
raised to as high
as 3.000 to 5.000
ppm, the level of
MgSOJaq) may
exceed the Me?*
level
Negligible







Negligible







Can affect the
K2SOtlaq) level.
Will not, however.
affect the total
soluble level of K


Negligible





Can affect the
NaxSOt/aq) level.
Will not, however.
affect the total
soluble level of Na

ZnSOtlaq) may
become predominant
at a pH around 9
when Cl ~and OH'
complexes are not
significant




Negligible







Negligible







If the redox poten-
tial is controlled
by sulfate/sulfite
species, sulfite oxi-
dation can increase
the soluble Mg level


Will increase the
KiSOtfaq) level
and reduce the K*
level, but will not
have a significant
effect on total
soluble K
If the redox potential
is controlled by sul-
fate/sulfite species.
sulfite oxidation can
increase the soluble
Se level
Will increase the
NaiSOtlaq) level and
reduce the Na* level.
but will not have a
significant effect on
total soluble Na
Negligible









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Table 6.     Effects of Adding Chemical Compounds on the Speciation of FGD Sludge Constituents
 Constituent
                      Addition of
                        Lime
                                           Addition of
                                            Silicates
                                  Addition of
                               Hydrogen Sulfide
       Addition of
       Phosphates
                                                                                       Addition of
                                                                                      Magnesium
     At
     As
Cd
Ca
Cr
Cu
Fe
Pb
              Effect on total soluble
              A I is negligible
              Lime addition can cause
              more
              form, so reduce the
              total soluble As
              slightly
              When the lime dosage is
              higher than 1,500 ppm,
              soluble Cd can be
              increased from 0.01 ppb
              to 1.45 ppb
              When the dosage of lime
              is from 100 to 1O,000
              ppm, the total soluble
              Ca will increase from
              200 ppm to 400 ppm
              Lime addition tends to
              increase the total
              soluble Cr because of
              hydroxide complexes
              formation
              Lime addition tends to
              increase soluble Cu but
              will  not raise the
              soluble Cu above  the
              detectable level
              When the lime dosage is
              higher than 1,500 ppm,
              the soluble Fe level will
              be increased from 0.012
              ppb  to 22 ppb
              Lime addition tends to
              increase the total sol-
              uble Pb because of car-
              bonate complex formation
                                    The soluble Al level can
                                    be greatly reduced when
                                    silicate addition is
                                    higher than 280 ppm as
                                    Si
                                    Negligible
Negligible
                                    Negligible
Negligible
                                    Negligible
                                    Negligible
                                    Negligible
                           Negligible
                           Negligible
                           Cd can be reduced to
                           trace levels when sul-
                           fide addition is higher
                           than 0.2 ppm

                           Negligible
                                                              Negligible
                           Cu can be reduced to
                           trace levels by adding
                           as little as 0.001 ppm
                           of sulfide

                           Negligible
                          Pb can be reduced to
                          trace levels by adding
                          as little as 0.001 ppm
                          of sulfide
                                                     Effect on total soluble
                                                     AI is negligible
Negligible
When phosphate addition
is higher than 310 ppm
fas PI, the soluble Cd
can be increased about
2 times
If phosphate addition is
higher than 310 ppm
(as P), soluble Ca can
be reduced slightly

Negligible
                                                                                         Negligible
                                                     Negligible
Negligible
                           Will not affect the total
                           soluble AI
                                                                                                                         Will not affect the total
                                                                                                                         soluble As
                                                                                                                    Will not affect the total
                                                                                                                    soluble Cd
                                                                               Magnesium addition may
                                                                               decrease the Ca-S04
                                                                               and Ca-F complexes but
                                                                               will not change the total
                                                                               soluble Ca
                                                                               May affect the total solu-
                                                                               ble Cr through the CrF1*
                                                                               reduction
                           Will not affect the total
                           soluble Cu
                           Will not affect the total
                           soluble Fe
                                                                               Will not affect the total
                                                                               soluble Pb
Mg





Mn


Hg



K



Se



Na



Zn



Lime addition will only
affect the total soluble
Mg slightly but will
significantly transform
Mg-C03 complexes

Lime addition tends to
reduce the soluble Mn
to the 20-36 ppb range
Lime addition tends to
increase the total sol-
uble Hg slightly because
of an increase in pH
Negligible



Lime addition will in-
crease the total soluble
Se because of an
increase in pH
Negligible



Lime addition may
increase the total
soluble Zn to ppm
levels
Negligible





Negligible


Negligible



Negligible



Negligible



Negligible



The soluble Zn level
is reduced when sili-
cate addition exceeds
280 ppm as Si
Negligible





Negligible


Hg can be reduced to
trace levels by adding
as little as 0.001 ppm
of sulfide
Negligible



Negligible



Negligible



Zn will be reduced to
trace levels when sul-
fide addition is higher
than 0.5 ppm
Soluble Mg will be
reduced about 2 5
times as the phos-
phate level is
increased from 0.3
to 3,100 ppm (as PI
Negligible


Negligible



Negligible



Negligible



Negligible



Negligible



Will cause the increase of
soluble Mg




Will not affect the total
soluble Mn

Will not affect the total
soluble Hg


Magnesium addition may
decrease the KiSOJaql
level but will not affect
the total soluble K
Will not affect the total
soluble Se


Magnesium addition may
decrease the NaiSOJaql
level but will not affect
the total soluble Na
Will not affect the total
soluble Zn



-------
James Lu is with Cal Science Research, Inc., Huntington Beach, CA 92647.
Donald E. Sanning is the EPA Project Officer (see below).
The complete report, entitled "Chemical Speciation of Flue Gas Desulfurization
  (FGD) Sludge Constituents," (Order No. PB 81-187 205; Cost: $24.50, subject
  to change) will be available only from:
        National Technical Information Service
        5285 Port Royal Road
        Springfield, VA 22161
        Telephone: 703-487-4650
The EPA Project Officer can be contacted at:
        Municipal Environmental Research Laboratory
        U.S. Environmental Protection Agency
        Cincinnati, OH 45268
                              10
                                                                             ft U.S. GOVERNMENT PRINTING OFFICE: 1W1 -757-01Z/7218

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