United States
                   Environmental Protection
                   Agency
Risk Reduction
Engineering Laboratory
Cincinnati OH 45268
                   Research and Development
EPA/600/S2-89/056  Jan. 1990
&EPA         Project  Summary

                   The Morphology  and
                   Microchemistry of
                   Solidified/Stabilized
                   Hazardous Waste  Systems
                  F. K, Cartledge, H. C. Eaton, M. E. Tittlebaum
                    A study was carried out to gather
                  data that can be interpreted in terms
                  of the mechanisms operating during
                  cementitious solidification/stabiliza-
                  tion of  hazardous waste  streams
                  containing water-soluble organics.
                  Most of the work was carried out with
                  phenols and ethylene glycol  as the
                  model wastes and Type I  Portland
                  cement as the fixing agent. Solidified
                  products containing from 2% to 50%
                  by  weight of organics  (measured
                  relative to cement) were studied at
                  various cure time up to 1 year. The
                  products were studied at various time
                  Intervals using  extractions with
                  solvents of  varying polarity, optical
                  microscopy, scanning  electron
                  microscopy and energy dispersive
                  elemental analysis,  transmission
                  electron microscopy,  x-ray  powder
                  diffraction, and several physical tests
                  (setting  times and unconfined com-
                  pressive strength).
                    The report describes and interprets
                  effects  of  the organics on the
                  developing cement matrix  and the
                  nature of the interactions involved.
                  The organics were not effectively im-
                  mobilized toward  water  leaching.
                  Depending on the chemical nature of
                  the organic,  the distribution  of the
                  model waste in  the cement  matrix
                  was either homogeneous  at the
                  micron level or quite heterogeneous.
                  Effects on the matrix were very con-
                  centration dependent and were much
                  more dramatic with ethylene glycol
                  than with the phenols. These effects
                  ranged from microscopic changes in
                  morphologies and compositions  of
cement phases to macroscopic prop-
erties such as compressive strength.
Although there was  evidence  of
chemical reaction between the phe-
nols and the fixing agents (spe-
cifically, salt formation), the reaction
did not result in chemical  fixation of
the organic.
  At low concentrations, the organics
did not greatly alter the  hydration
chemistry of the cement system. The
probable consequence of this would
be  little  interference in  immo-
bilization of inorganics in cases in
which mixed inorganic/organic waste
streams are encountered. Specific
experiments designed  to test this
conclusion, however, have not yet
been carried out.
  This Project Summary was  devel-
oped by EPA's Risk  Reduction Engi-
neering Laboratory, Cincinnati, OH, to
announce key findings of the research
project that is fully documented in a
separate report of the same title (see
Project Report ordering Information at
back).

Introduction
  The report summarized here describes
the first of three phases of work aimed at
thoroughly  characterizing wastes
solidified in a cement matrix, or whatever.
Phase I, the fundamental research aspect
of the work is an effort to  understand
solidification mechanisms with the use of
cement and  several water-soluble
organics. Phase II is  an extension of
Phase I and involves cooperation with the
Waterways Experiment Station  of the
U.S. Army Corps of Engineers (WES) in a

-------
project to characterize interferences  by
various inorganic and organic materials in
solidification of metal sludges with  the
use of cement and fly ash fixing agents.
Phase III of the work involves the use of
x-ray diffraction  (XRD)  and scanning
electron  microscopy (SEM) to  charac-
terize vendor-produced samples  of
wastes solidified by processes, which are
usually proprietary. Phase III is a part of
the U.S.  EPA/Environment  Canada joint
project  to  evaluate test methods  for
solidified products. Phases  II  and  III are
not completed and  will be  described in
detail in a future report.
  Solidification/stabilization is a common
technology  used  to  immobilize wastes
before landfilling, roadbed  construction,
etc. The technology  has been  most com-
monly studied as a potential technique to
immobilize toxic metal ions or  radioactive
waste. Complete detoxification of metals
by chemical, biological, or other means is
impossible short of  elemental  trans-
formation; hence, methods that  dilute
and/or isolate the metals are necessary
as part of waste management schemes.
Although many  vendors  of  solidification/
stabilization technology have  presented
leaching  data  claiming the  efficacy  of
various immobilization techniques, claims
concerning  the  nature of  chemical
interactions between waste  metal ions
and  fixing  agents  have  remained  un-
substantiated.
  The aim of the Phase I research was to
gain information  about the  mechanisms
by  which  solidification/stabilization
schemes operate and to define the nature
of the interferences associated with the
presence of  various classes of com-
pounds,  both inorganic and organic.
Conceptually,  there are  two  broad
classes of mechanisms; namely, physical
entrapment  and  chemical interaction.
Physical tests, spectroscopy, and micros-
copy all  were used  to gain  information
about the  interactions  of various
compounds with typical solidification/
stabilization matrices.
  The two principal  constituents of most
commercial fixing agents are cementi-
tious materials (Portland  cement, fly ash,
etc.)  and soluble silicates. A limitation
often cited is that  the   processes  are
incompatible  with organics,  but  details
about the types of organics that interfere
or  the  concentrations at  which  inter-
ference  is detrimental are not available.
The same is  true with  many inorganic
materials. A  potential concern  is that
interferences, even in small amounts, can
alter the process  sufficiently to  sub-
stantially decrease the ability of the fixing
agents to immobilize metal ions. Indeed,
it is well known that admixtures can alter
the setting characteristics of Portland
cement. It is not clear whether,  and at
what concentrations,  various materials
commonly  present in waste streams
interfere  with the  complex  setting
reactions and result  in a significantly
altered cement matrix. The question is of
obvious interest with respect to solidifica-
tion/stabilization technology, since com-
plex mixed  inorganic/organic  waste
streams are commonly encountered.

Research  Methods
  The  methods used  in  Phase  I were
adaptations of procedures  used to char-
acterize  cement  (or  other inorganic)
matrices, as  well as common techniques
to characterize  solidified waste form.
Samples  were  prepared  using  Type  I
Portland cement in a 0.4 watercement
ratio. The organic compounds were ethyl-
ene glycol  (EG),  p-bromophenol (pBP),
and p-chlorophenol (pCP). The required
amount of organic  compound  (0.2 g, 0.4
g, 1.0 g, or 2.0 g) was  weighed out into a
screw-cap vial, and 10.0 mL of Portland
cement was added followed by 4.0 ml of
deionized water. The mixture was stirred
with a glass  stirring rod, for 1  minute by
hand. The vials were allowed to stand in
the dark at room temperature for periods
of from 12 hours to 1  year before being
tested.
  The  test methods and the information
they were expected to afford  are briefly
summarized  here:

Extraction with Solvents of
Varying Polarity
  The  samples containing various con-
centrations of organics were ground to a
standard  size  and extracted  with three
solvents: dichloromethane (DCM), di-
methyl sulfoxide (DMSO), and deionized
water. The amount of organic  compound
recovered in  the  extractions was  deter-
mined  as a function of solvent polarity
and time of cure for the sample. The data
were  used  to reach qualitative  con-
clusions concerning the environment of
the organic  compound  in the  cement
structure, and trends in  extractability
were compared  with  qualitative differ-
ences  in sample  morphological compo-
sition observed by microscopy.

Microscopy (Optical and SEM)
and Energy-Dispersive X-Ray
Analysis (EDXA)
  Optical and SEM observations  of  sur-
faces of solidified samples were made to
characterize  changes occurring as  a
result of having added wastes to cerr
Because numerous  micrographs  I
been  published  for cements alone
with various additives, a large amoui
data are available for comparisons. E
can provide an elemental profile i
solid  surface,  with certain limitati
These methods in combination with tl
described below can determine whe
the waste has influenced the formatic
the mineral  phases characteristic  of
matrix.

Transmission Electron
Microscopy (TEM) and Select
Area Diffraction (SAD)
  TEM has been used to  study cer<
materials and  minerals for the pas
years,  and several studies of cer
have been  reported. TEM, however,
not been applied to studies  of solid
hazardous  chemical wastes.  The  r
advantage  of TEM is  the high  sp
resolution, which can exceed 0.2 nn
addition,  the SAD pattern can pro
information about  crystal  structure
the orientation of crystalline phases. I
of these  instrumental  characteristics
important for waste research.

X-Ray Powder Diffraction (XR
  Powder diffraction analysis allows
crystalline  mineral constituents  of
matrix  to  be identified  by  t
characteristic  set  of  diffraction  li
Many XRD studies  of cements have t
carried out.  Although  limitations
associated with the complex nature o
formed  solid  matrix,  some min
constituents are easily identifiable.
presence or absence of specific mil
phases can be a function of admixtun
the  cement  formulation;  that
presumably also  be  the case  w
wastes are the admixtures.

Physical  Testing
  Selected physical characteristics o
solidified samples  have been studie
define strength and practical workal
of waste/cement  mixes.  Specific
compressive strengths  and setting ti
(initial  and final) of cements contai
organics  were  studied. The compre:
strength  test  reflects the  amoun
applied loading the solidified wastes
withstand before failure in  a landfill.
setting  time tests indicate  the
needed  for the solidified  waste
become workable. In addition, these
were conducted because they have
been  used  by  the cement  industr
standard  indicators of mechar
performance.

-------
The Use of Polar Organlcs
  Most of the Phase 1 studies involved
relatively  polar  organic  molecules,
although some  preliminary work with
nonpolar organics  is  also  reported.
Because of their relatively high water
solubility, polar organics are the  ones
most likely to be present in substantial
concentrations in  mixed aqueous waste
streams  that also contain metal  ions.
Thus, polar organics are good candidates
as solidification/stabilization interferences.
Glycols  and phenols are typical of such
species and are  also major articles of
commerce  and,  hence,  constituents of
waste streams. Apart from the  fact that
EG, pCP, and  pBP are typical  of  real
wastes,  the reason for  choosing  halo-
genated phenols is that the presence of
the heavy  atoms  enables elemental
analysis  by EDXA to locate the  organic
within the  complex hydrated  cement
matrix.
  These  polyhydroxy compounds are, in
fact, among the classes  of organics that
alter the  setting  characteristics  of
Portland cement.  The polyhydroxy
organic  EG was  chosen  for  several
reasons.  There is evidence in the litera-
ture that EG  has profound effects  on
already  set cement and the  mineral
constituents thereof. When  hydrated
;ement  of tricalcium silicate  (C/S) is
.reated with EG, etching  occurs, but it is
unclear  whether  mainly  calcium silicate
hydrate  gel (CSH) or calcium hydroxide
(CH) is dissolved. A further consideration
is  that EG is  completely  miscible with
water. Hence, cement  pastes  can  be
prepared with any concentration of EDG
in  water, and  in  all cases, a  homog-
eneous liquid phase is being mixed with
the unhydrated cement. The mixing prob-
lems  are  also   minimized  with  the
phenols,  which are substantially water
soluble.  When the very  water-in-soluble
organic  1-decanol was solidified, as the
right ratio of organic to cement  varied
from 50:1 to 1:1, the product of solid-
ification  varied from a solid, which was
outwardly indistinguishable from hard-
ened cement, to a two-phase system with
hardened material and supernatant liquid
(shown by gas chromatograph analysis to
be  pure 1-decanol).  With  the  EG
samples, there was great variation in the
physical  appearance of  the  mixes  as
functions of both concentration and time
of cure.

Results and Discussion
  The systems studied in Phase I repre-
sent the most thoroughly  characterized
combinations of organics  and cement
pastes.  In  particular,  the  combinations
included those  with relatively high con-
centrations of organics—those typical of
situations  in which organics would con-
stitute a large fraction  of a waste mixture
being solidified. Two questions concern-
ing the  Phase  I study  of  organics are
particularly relevant to solidification prac-
tice:

1.  Do cementitious  matrices have the
    ability  to immobilize  the  organics
    themselves?
2.  How  do organics  alter the cement
    matrix and thus  affect immobilization
    of inorganic  constituents?

  The  Phase  I study  has effectively
demonstrated that cement alone is inef-
fective  in  immobilizing water-soluble
organics such as EG or  phenols. The
second  question is  not completely an-
swered to date.  Although many  effects of
organics on the cement matrix at various
concentrations have been  documented.
The leaching studies  needed to  deter-
mine whether  the  organics constitute
interferences in inorganic immobilization
remain to be carried  out or interpreted.
Phases  II and  III will report on  some
leaching studies at 3 later date.
  The following  paragraphs summarize
the information obtained thus far.

EGlCement
1.  For ratios of up to 1:5 EG:cement, the
    same  basic reaction chemistry went
    on  during cement hydration in the
    presence  or absence  of EG.  SEMI
    EDX analysis was able to  identify
    phases apparently identical to those
    in hydrated cement  alone  (although
    not necessarily in  the  same propor-
    tions as in  cement  alone).  At con-
    centrations of 1:5 and  greater, the
    samples did not effectively set even
    at 28 days or longer.
2.  EG  slowed  the  rate of hydration of
    cement, even in the 1:50 mixtures. At
    1:5 ratios, final set was not reached.
3.  There  was  a small percentage  of
    strongly bound  (although mostly
    reversibly bound)  EG.   Solvents  in
    which  EG is very  soluble (DCM and
    DMSO) and that  penetrate the
    cement matrix very effectively  under
    our  extraction  conditions   did not
    always give  high recoveries of EG.
4.  Despite the statements in  the pre-
    ceding paragraph,  EG was not
    effectively immobilized  toward water
    leaching even at low loadings of EG
    on cement. High percentage recover-
    ies (up to 100% in a single extraction
    after  grinding)  were observed at all
    loadings of EG  on cement at all times
    of cure.
5.  The principal effect of  EG  on the
    microstructure of cement involved the
    CSH  gel  phase. There  were notice-
    able effects on the morphology of this
    phase,  particularly  the  presence of
    aggregates of small grains.  EG also
    appeared to absorb to the surfaces of
    Ca(OH)2 crystals. Fine  crystals with
    d-spacings uncharacteristic  of com-
    mon  cement phases could be ob-
    served, but not  identified by TEM.
6.  Overall crystalinity of the matrix was
    diminished with increasing EG con-
    centration, particularly  above  about
    10% EG by weight.
7.  Below 1:10 EG:cement,  28 day com-
    pressive strengths  were comparable
    with those of cement pastes  alone,
    but above 1:10 there were significant
    decreases in strength.
8.  Increasing  EG concentration in-
    creased  porosity of the matrix,  as
    judged qualitatively by SEM.


pCP/Cement
1.  Unconfined compressive strength of
    pCP/cement was lower  than for the
    control  at 7  days but was  approxi-
    mately equal at 28 days.
2.  Times for initial and final  set  were
    approximately doubled.  pCP slowed
    the hydration of cement more than
    did pBP but less than did EG.
3.  In 1:10 pCP:cement samples percent
    recovery  in  water  extraction  de-
    creased with  time of cure from 93%
    (12 hours) to 60%  (90  days). There
    was no  effective immobilization at
    any concentration or time of cure.
4.  SEM  showed  significant morpholog-
    ical differences of pCP/cement when
    compared with cement pastes: more
    porous at 12 and 24 hours  but less
    porous at 7 and 28 days.
5.  EDX  showed homogeneous  distribu-
    tion of Cl at the 10 p level.  pCP was
    not found in the CH  phase, and it was
    not found in a separate phase as was
    pBP.
6.  XRD  showed  new  peaks,  probably
    the Ca salt of pCP.
7.  XRD  showed significantly decreased
    crystalinity.
8.  Despite the observations above, pCP
    allowed the basic reaction chemistry
    of  setting cement to  proceed,  as
    shown by the presence of the normal
    cement mineral phases.

-------
pBP/Cement
1.   Unconfined compressive strength of
    pBP/cement was  lower than was the
    control  at 7 days but approximately
    equal at 28 days.
2.   Time  for initial  set  increased
    approximately 20%; time for final set
    increased approximately 75%.
3.   In 1:10 pBP:cement samples, percent
    recovery  in water extraction varied
    between  45% and  55%  over  the
    period from 12 hours to 90 days, but
    dropped to a low of 9%  at 1 year.
    Again, effective immobilization was
    not achieved  at any concentration or
    any time of cure.
4.   Electron  Probe Micro  Analysis
    showed  inhomogeneous distribution
    of Br at the  10 n level. There were
    distinct Br-rich phases, presumably
    the Ca salt.
5.   XRD  showed  new peaks, probably
    the Ca salt of pBP.
6.   XRD  showed  significantly decreased
    crystalinity.
7.   The presence of pBP  allowed  the
    basic reaction chemistry  of setting
    cement to proceed.

Conclusions
  Clearly neither the phenols used in this
study nor ethylene glycol was effectively
immobilized  by   cement alone  at  any
concentration studied. We  assume  that
this  will  also be  the case  with other
relatively  water-soluble organics. The
only evidence of  reaction  between  the
organics  and the  fixing medium was salt
formation.  Indeed, when  salt formation
occurred, as  in the case of the phenols,
the  organic  remained relatively water
soluble and easily extractable from the
solidified matrix.  There appeared to  be
several distinguishable environments  for
the organics in the cement matrix:

1.   a separate microscopically distin-
    guishable phase,  as with  the Ca salt
    of pBP; as such, it was easily ex-
    tractable.
2.  an  environment from which the  or-
   ganic was  rather easily  extracted by
   water but not by less polar solvents;
   probably involved hydrogen bonding
   by  the organic hydroxy  groups in
   interlayer spaces of CSH gel.
3.  an  environment in which the organic
   was quite  loosely bound  and  easily
   extracted by any solvent  in which it
   was moderately soluble; this environ-
   ment may  also  have  involved the
   CSH phase.

  The idea that there is a definite number
of  binding sites in  the cement matrix at
which  the organic  may be  effectively
immobilized  was not borne out by our
work. Even at the  lowest concentrations
of  organics in the  cement  matrix,  water
extracted the organics efficiently.
  The cement matrix was affected in dra-
matic ways by the  presence of organics.
Presumably  the ability of the matrix to
contain other wastes, such as metal ions,
will also be  affected by the changes
induced by the presence of organics. The
matrix  changes depended on the nature
and the concentration of the organic. The
changes in  easily  observable or meas-
urable  properties  of the  matrix  were
greatest  with  EG,  less  with pCP, and
least with pBP. At or below a 1:10 ratio of
organic to cement,  the effects of all  three
organics on  the easily measurable  prop-
erties of the  matrix were rather minor. All
gave homogeneous matrices that looked
like set cement; set times were affected
to  a significant degree  by  EG but  not
much  by pCP and pBP;  compressive
strengths at  28 days were comparable to
those of cement pastes without additives.
Nevertheless, while SEM, TEM, and XRD
indicated  that some  cement  hydration
reactions were  taking place in the  same
way  that they do in the absence of the
organics, the  situation was much  more
complex. New  phases were formed; the
usual phases appeared  to undergo solid
solution  formation  giving  shifted  XRD
peaks;  new  morphologies appeared with
increasing frequency and increasing con-
centration  of  organics. Although
changes can be documented, the effi
of such changes  on  some of
measurable properties, particularly  c
pressive strength, were minor. The n
important point would be  whether
changes affected the immobilizing at
of the matrix toward  a variety of was
Some information of the latter kind she
be available from the WES project:
results of our  participation  in  that v
will be  reported as Phase II of
project.
  Nevertheless, additional work need;
be done to bridge the gap between
work done here and  field application!
solidification  technology. Cementiti
solidification/stabilization is  most  c>
monly used to  immobilize metal ions.
are now investigating the effectivenes
immobilization, as measured by Toxi
Characteristics  Leaching  Prpced
(TCLP),  as various  metal contair
wastes  are solidified,  increasing
waste-to-cement  ratios gradually i
failure  occurs.  At  the same   ti
increasing  amounts  of  organic   in
ferences are being added. In additioi
monitoring  metal  and  organic  c
centration in TCLP leachates, the  m;
changes are being monitored  using
techniques  developed in this study.
can thus have a thorough characteriza
of the  matrix  in  cases  where
mobilization if effective and  can  w;
changes in the matrix that occur  as
approach failure of the system. We c<
thereby  identify  what changes
associated  with decreasing  (or incn
ing) effectiveness of immobilization.
  The full  report was submitted  in
fillment of Contract No.  CR 812318-1
by Louisiana  State University  under
sponsorship of the  U.S. Environme
Protection Agency.

-------
 F. K. Cartledge,  H.  C. Eaton, and M. E. Tittlebaum are with Louisiana  State
  University, Baton Rouge, LA 70803.
 Charles I. Mashnl is the EPA Protect Officer (see below).
 The complete report, entitled  "The  Morphology and Microchemistry of
  Solidified/Stabilized Hazardous Waste Systems," (Order No. PB 90-134 156/AS;
  Cost: $23.00, 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:
        Risk Reduction Engineering Laboratory
        U.S. Environmental Protection Agency
        Cincinnati, OH 45268
United States
Environmental Protection
Agency
Center for Environmental Research
Information
Cincinnati OH 45268
      BULK RATE
POSTAGE & FEES PAIC
         EPA
   PERMIT No. G-35
Official Business
Penalty for Private Use $300

EPA/600/S2-89/056
                 000085956
                                                       130

                                                60604

-------