vvEPA
                             United States
                             Environmental Protection
                             Agency
                                Risk Reduction
                                Engineering Laboratory
                                Cincinnati OH 45268
                             Research and Development
                                EPA/600/M-89/023  Jan. 1990
ENVIRONMENTAL
RESEARCH  BRIEF
               Predicting Movement of Selected Metals in Soil:
                        Application to Disposal Problems
                                    Hinton K. Howard*
Abstract
Data from  laboratory column studies  of movement of
selected metals in municipal solid waste (MSW) leachate
through soils from several parts of the United States were
used as a base for developing simple, field-oriented tools
for predicting pollutant  movement.  The metals studied
were arsenic, beryllium, cadmium,  chromium, copper,
iron, mercury, nickel, lead, selenium, vanadium, and zinc.
Principal variables in the laboratory study and in the
models were 1. Physical/chemical properties of soil such
as clay content, pH, and iron/manganese hydrous oxide
content, and 2. Leachate properties such as total organic
carbon (TOC) and total salts.
The first model was based on the Lapidus and Amundson
(L-A) equation. A simpler, more adaptable model based
on the Error Function equation was also developed and
tested. Both models effectively predicted rates of metal
movement  through soil  in MSW leachates, but the L-A
method of  developing  the model was  somewhat more
difficult in terms of the amount of input data and param-
eter estimation.
"Risk Reduction Engineering Laboratory, U S Environmental Protection
 Agency, Cincinnati, OH 45268
                Work was  also conducted on movement in soil of the
                natural phenolic fraction  of MSW leachate and of six
                monohydroxybenzene derivatives of phenol  added to
                MSW leachate. Movement rates and the soil  and leachate
                characteristics that influenced the rates were identified;
                the results have not been incorporated into the model.
                This  Research  Brief was  developed  by  EPA's  Risk
                Reduction  Engineering Laboratory, Cincinnati, OH, to
                announce key findings of the research projects that are
                fully documented in separate reports and journal articles.

                Introduction
                The composition  of landfill  leachate and  the charac-
                teristics/composition of the  soil  determine  the rate at
                which metals in the leachate migrate through the soil.
                Having the capability to predict migration rates based on
                a knowledge of the leachate and soil characteristics would
                greatly aid in the design  of landfills. The first section of
                this Research Brief outlines the small-scale soil column
                experiments that  measured migration rates of various
                materials through a variety of soils and the  development
                of  equations for  predicting  leachate migration rates in
                soils. The  work builds on  the  results of a  previous
                literature survey (1) and  laboratory soil column studies
                with MSW leachate (2,3,4) by Dr.  Wallace H. Fuller et al.,

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at the University of Arizona.  The second section presents
information concerning adsorption and movement in soils
of the phenolic fraction of MSW leachate.

No  field  data were  available to  test the  equations  for
predicting leachate  migration rates.  It is thought  that
models based on laboratory  soil column data  are capable
of making qualitative predictions (relative migration rates,
etc.) but are  much  less  accurate  for quantitative pre-
dictions. The hydraulic characteristics of a  laboratory soil
column may not be  very representative of field conditions
because  1. removing  a  soil  sample from the  ground and
placing it in a column can alter the sample  physically and
2. the sample(s) size or numbers  may not  be  sufficient to
represent the total ground area of interest.  The adsorptive
characteristics of a soil sample will, however, represent the
field characteristics unless the adsorptive process is slow
and  the  contact  times  (between  leachate  and  soil)  are
different in the laboratory than in the field

Models  based  on laboratory soil  column   data  may  not
quantitatively predict migration in field soils Nevertheless,
predictions of extremes based on laboratory  data  can
provide important perspective concerning pollutant migra-
tion  in the field, e g.,  identifying contaminants or soil/
leachate conditions  that will  produce  slow  or rapid
migration.

Soil Column Procedure
The several experiments covered in this publication took
place during the period 1976-1982  The   same  general
procedures,  as  described  below,  were  used for   all
experiments,  with variations  introduced as required  for
specific experiments.

Leachate was generated in 4000-L containers  packed with
materials representative of those found in municipal waste
After packing, the containers were filled with water and the
resulting  mix was allowed to age.  Leachate  was  withdrawn
from the bottom of the tank anaerobically and stored under
a blanket of carbon dioxide.  Leachate was  spiked with  the
metals of interest and applied to the 5-cm-diameter x  10-
cm-length  packed   columns using  a constant  head
apparatus that supplied  a blanket of  carbon dioxide  to
prevent oxidation/precipitation of  leachate components.
Leaching through the soils was continued until  one of three
conditions was met: breakthrough (effluent concentration
 = influent concentration), steady state (unchanging or very
slowly changing effluent concentration);  or  continued
absence  of  a trace  metal after  extended  leaching  The
trace element content of the leachate was determined and
used  to  calculate a  correlation  matrix  and a multiple
regression  analysis  of  trace metal mobility  versus  soil
properties.

The soils used in the experiments, obtained from different
regions of the United States, exhibited a  wide range of
composition and characteristics (Table 1). Before  being
packed  into 5-cm-diameter x 10-cm- length columns, the
soils were air  dried  and passed through 0 5-mm screens.
Soil columns were perfused with  either constant head or
constant flux, depending  upon  the specific experimental
objectives.

Metals Migration
The metals used in the soil properties study  (5,6) were
arsenic, beryllium, cadmium, chromium, copper, mercury,
nickel, lead,  selenium,  vanadium,  and zinc.  This study
investigated the effect of soil properties, leachate  proper-
ties, and leachate flow rates on Metal Migration

So/7 Properties
There  were 11  different soils from  7 orders in  the  Soil
Taxonomy  classification system. The  best correlation  with
mobility was obtained  for the  percent clay  in  a  soil,
followed in order by the surface area and the percentage
of free iron oxides. The researchers concluded that, even
though the mobilities of trace metals differed significantly,
qualitatively predicting mobility on the basis  of these soil
properties should be possible.

Leachate  Properties
The leachate  properties studies (4,5,7,8)  examined  the
movement  of salts  of  cadmium,  iron, nickel, and  zinc
through six soils (see Table 1). The leachate composition
variables were  total organic carbon (TOG), total inorganic
salts (SALT), and iron (Fe).

Leachate was displaced through the  soil under saturated
anaerobic  conditions  at constant flux rates. Influent  and
effluent analysis at set time intervals provided the basis for
conclusions  concerning  the  influence of  the  various
parameters on metal migration.

For each of the four metals in all of the soils it was found
that the  rate  of migration  was  higher when  the con-
centration of any of the three parameters (TOC, SALT, Fe)
was higher. The quantitative  results from these  studies
were  used to  develop  equations for predicting  metals
migration.

Leachate  Flow Rate
In the leachate flow  rate studies (9,10), leachates were
individually enriched with  salts  of  arsenic,  beryllium,
cadmium, chromium, iron, nickel, and zinc and displaced
through soils  under anaerobic saturated conditions  with
controlled  flow rates  from 12 to  18  cm/day. Nine  soils
were  used. Effluent  collected  at  hourly  intervals  was
analyzed  for  the  metal ions of  interest.  Solution
displacements  continued  until  the concentration  of the
metal in the effluent equaled that of the influent.

In general, the   results  showed that  the slower the  flux,
the lower the concentration of  metals in the effluent  at a
given  number  of pore  volume  displacements.  The
magnitude  of  the  effect was large  for arsenic, beryllium,
chromium, and  iron ions; and  small  for cadmium, nickel
and zinc ions.

Prediction Equations
The general method  to  develop prediction equations
(11,12) was regression analysis with the use  of movement
rates for Ni, Cd, and Zn from the soil column studies  Soil
and leachate properties were used  to obtain coefficients
for the prediction equation.

The predictive  equation developed from the error  function
model was:
       C/Co = 0.5 erfc [(Rz-vt)/(4DRt)0 &]
[1]
 where C is the solute concentration  in soil water at time t
 and depth z,  Co is the solute concentration in the input

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Table 1.   Soil Properties*

           Iron
Soil Clay Surface
Oxide
Series (%) (%) (M2/g)
Davidson
Molokai
Nicholson
Fanno
Mohave (Ca)
Chalmers
Ava
Anthony
Mohave
Wag ram
Kalkaska
17
23
5.6
3.7
2.5
3.1
4
1.8
1.7
0.6
1.8
52
52
49
46
40
31
31
15
11
4
5
51
67
120
122
128
96
62
20
38
8
9
Dominant
Clay Minerals
Kaolin. +
Kaolin., Gibbs.
Vermic.
Mont, mica
Mica, Mont.
Mont., Vermic.
Vermic., Kaolin.
Mont, mica
Mica, Kaolin.
Kaolin., Chlor.
Chlor., Kaolin.
Texture
(USDA)
Cl.
Cl.
Si. Cl.
Cl.
Cl. loam
Si Cl loam
Si Cl loam
Sandy loam
Cl. loam
Loamy sand
Sand
 "Most common values cited  in the references at the end of this
Research Brief.
 + CI #-Clay;  Si #-Silty; Mont.  #-Montmonllonite;  Kaolin.-Kaolnite;
  Gibbs.-Gibbsite; Chlor.-Chlonte; Vermic.-Vermicuhte

solution; z is the depth; t is the time; v is the pore water
velocity; R is the retardation factor (dimensionless); D is
the diffusion coefficient (units  12/t);  and  erfc  is  the
complementary error function.  The user obtains  values
for  D and R from regression equations [2] of the form:
       V = C1P1 +  C2P2 +  C3P3  +
[2]
where V is the value for D or R to be used in equation [1];
C1, C2, C3,  etc.,  are  coefficients that  were developed
from regression analysis of the soil column data, and P1,
P2, P3,  etc., are soil and leachate properties such as clay
content, TOG, etc.,  supplied  by  the user.  One  set  of
coefficients (Cl, C2, C3, etc.) was developed for each
metal when it is the only solute of interest in the leachate,
and another set  is to be used when one or more other
competing metals are present in the leachate.
The predictive equations developed from the L-A model
(3) are of the form:
       V.# =(v/25)[C1P1  +C2P2 +  C3P3  + ...]
[3]
where  V.# is the  velocity of  the  relative  solute
concentration (C/Co), e.g. # = 0.1, 0.2, 0.3, etc.;  v is the
pore water velocity (seepage  velocity);  C1, C2, C3,  etc.,
are regression  coefficients  calculated  from the  soil
column  data; and  P1, P2, P3,  etc., are properties  such as
clay and  iron  oxide  content  in soil  and TOC and salt
concentration  in  leachate.  There is  one set  of the
regression coefficients for each metal and for each of 10
relative  concentrations (0.1, 0.2,...0.8, 0.9). Additionally, a
second  set of  coefficients was developed for use when
one or  more  competing  metals are  present  in  the
leachate along  with the metal of interest
The results provide a simple set of equations that can be
quickly calculated without the  aid of a computer. Although
no  field test has  been conducted  to date, it should be
noted that the equations were  based on soils with a great
variety  of  chemical  and  physical  properties.  This
suggests that the results will be broadly applicable,
particularly where exact values are not of interest (as in
screening studies).

Phenols Migration/Adsorption
Phenols are water contaminants  both because of their
toxicity  and because they may,  at low concentrations,
render  drinking  water unpotable due  to  their strong
taste and odor. Simple phenols (monohydroxybenzene
derivatives)  are  found  in  soil  as  a  result of  the
decomposition  and  disposal  of  organic  wastes,
biological  synthesis, and  the breakdown  of aromatic
pesticides.  Lakes  and lagoons  used  by  paper  mill
industries for disposal of large amounts of  delignified
wood wastes  contain  abundant  natural phenols. Oil
refineries and coke plants also separate  and  dispose of
large amounts  of  phenols  from  coal tar  wastes.
Industries dealing in  the manufacturing  and use of
medicinals,  dyes,  resins,  perfumes,  explosives,
disinfectants, and photodevelopers use and  dispose of
sizable  quantities of  phenols  of  both  natural  and
synthetic origin.
In the  phenol  studies  (13, 14),  the  parameters
investigated  were  phenol  concentration  in  MSW
leachates  versus  leachate  age,  effect  of   soil
composition on attenuation, and the effect of aeration.

Adsorption
Six  different  monohydroxybenzene derivatives
(phenols) at concentrations from  5 to 200 ppm  in water
were mixed with small amounts of  five different  soil
samples with which contact was maintained for up to
14 days. The amount of the various phenols adsorbed
on each soil  was measured, and the results were
correlated with soil properties. The characteristics  that
correlated most highly were, in order, level of free  iron
oxide, pH, and percent clay.

Concentration versus Age
The natural phenol levels in Carbon  dioxide-blanketed
leachates ranging from 1  to  7 yr old were  monitored
over a  12-mo  period.  The  phenol  concentration
dropped considerably  in  the  1-year-old  (initially)
leachate but  remained relatively constant in  5-yr-old
and 7-yr-old leachate. Even in the older leachates, the
level remained  at 40  to 90  times higher  than that of
drinking water standards,  leading to the conclusion  that
MSW landfill leachates retained large quantities of
natural phenols in solution, whether they are young or
old.

Soil Composition
Anaerobic constant flux soil column experiments were
run using the natural  leachate  as  well as  leachates
enriched with specific phenols.  The  overall results
showed  that  soils with higher iron levels were  more
effective at  attenuating phenol  migration.  Also,  high
TOC levels and low pH in leachates correlate with  low
retention of phenols by soils.

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Aeration
Enriched leachates were stored under carbon dioxide and
also bubbled with air for 15 days. The phenol levels in the
air-aerated samples  were significantly reduced when
compared with  the  levels  in the carbon dioxide covered
samples except  for  nitrophenol, which  showed  little
reactivity.

The references  listed below  are reports  and  articles
submitted in partial fulfillment of Contract 68-03-0208 and
Grants R805731 and R803988 by the  University of Arizona
under the sponsorship of the U.S. Environmental Protec-
tion Agency. The Principal  Investigator was Dr. Wallace H.
Fuller of the University of Arizona,  Tucson, AZ 85721.
Michael H. Roulier was the  EPA Project Officer.

The EPA reports  and symposium proceedings  are avail-
able only from:
      National Technical Information Service
      5285 Port Royal Road
      Springfield, VA 22161
      Telephone: 703-487-4650

The NTIS order numbers  are listed  at  the  end of  each
reference citation. The other references were published in
journals, as noted, and are available at many libraries.


References
 1.  Fuller, W.  H. 1977. Movement  of  selected  metals,
    asbestos, and cyanide in soil: applications to disposal
    problems. (EPA-600/2-77-020) U.S. Environmental  Pro-
    tection Agency, Cincinnati,  OH 45268.  NTIS  No. PB
    266 905.
 2.  Fuller, W.  H. 1978. Investigation of landfill leachate
    pollutant attenuation by soils. (EPA-600/2-78-158)  U.S.
    Environmental  Protection  Agency,  Cincinnati,  OH
    45268. NTIS No. PB 286 995.
 3.  Fuller, W.  H.,  B.  A. Alesii, and  G.  E.  Carter. 1979.
    Behavior of municipal solid  waste leachate.  I.  Compo-
    sition variations. J. Environ. Sci.  Health, A14(6):  461-
    586.
                          4.  Fuller, W. H., A. Amoozegar-Fard, E. E. Niebla, and M.
                             Boyle. 1980. Influence of leachate quality on soil atten-
                             uation of metals,  p.  108-117.  In David  Schult;:  (ed.)
                             Proc. 6th Annual Res. Symposium,  Chicago, IL, 17-20
                             Mar.  1980.  (EPA  600/9-80-010).  U. S.  Environmental
                             Protection Agency, Cincinnati, OH 45268. NTIS No. PB
                             80-175-086.
                          5.  Fuller, W. H.,  and  B.  A.  Alesii. 1979. Behavior  of
                             municipal solid waste leachates. II.  In soil. J. Environ.
                             Sci. Health, A14(7): 559-592.
                          6.  Korte, N. E., J. Skopp, W.  H. Fuller, E.  E. Niebla, and
                             B.  A.  Alesii. 1976. Trace element  movement in  soil:
                             influence of soil physical and chemical properties. Soil
                             Sci. 122:350-359.
                          7.  Boyle, M., and W. H. Fuller.  1987.  Effect of municipal
                             solid  waste  leachate composition  on zinc migration
                             through soils. J. Environ. Qual. 16(4):357-360.
                          8.  Turjoman, A. M., and W. H.  Fuller.  1987. Behavior of
                             lead as  a migrating pollutant in  Saudi Arabian  soils.
                             Arid Soil Research and Rehabilitation, V31-45.
                          9.  Alesii, B. A., and W. H. Fuller, and  M. V. Boyle. 1980.
                             Effect of leachate flow rate on metal migration through
                             soil. J. Environ. Qual. 9:119-126.
                         10.  Fuller, W. H. 1981. Liners  of natural porous materials
                             to  minimize  pollutant migration.  (EPA-600/2-81-122)
                             U.S. Environmental Protection Agency, Cincmnali, OH
                             45268. NTIS No. PB 81-221-863.
                         11.  Amoozegar-Fard, A., A. W. Warrick, and W. H. Fuller.
                             1983. A  simplified model for solute  movement through
                             soils. Soil Sci. Soc. Am. J. 47:1047-1049.
                         12.  Amoozegar-Fard, A., W. H. Fuller, and A. W. Warrick.
                             1984.  An approach to predicting  the  movement  of
                             selected  polluting metals  in soils.   J. Environ.  Qual.
                             13:290-297.
                         13.  Artiola-Fortuny, J., and W. H. Fuller. 1982a. Phenols in
                             municipal solid  waste leachates and their attenuation
                             by clay soils. Soil Sci. 133:218-227.
                         14.  Artiola-Fortuny, J., and W. H. Fuller. 1982b. Adsorption
                             of  some monohydroxybenzene derivatives by  soils.
                             Soil Sci. 133:18-26.
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