United States
 Environmental Protection
 Agency
 Health Effects
 Research Laboratory
 Research Triangle Park, NC 27711
Research and Development
EPA-600/S1-84-026 Jan. 1985
Project  Summary
 Sorption  Properties  of  Model
 Compounds  on  Cis Adsorbents
 Harold F. Walton
  The bonded silica adsorbent, Bonda-
pak-Cis® (Waters Associates) has been
evaluated for removing organic matter
from secondary sewage effluents and
from solutions of pure organic com-
pounds. The adsorbent is hydrophobic
and will not function effectively in
water unless it is first wet with methanol
or another organic solvent;  therefore,
its behavior in water may be erratic. In
water-methanol mixtures on the other
hand it behaves reproducibly and gives
linear absorption isotherms. Advantages
of Bondapak-CiB®,  compared  with
microparticulate adsorbents, include
greater chemical robustness and toler-
ance to regeneration, lower flow resist-
ance and lower cost. It has been used to
remove organic compounds from water
and as  a  support in low-resolution
chromatographic analysis.
  Part of this effort was to develop
liquid-chromatographic methods of
analysis for  organic constituents of
wastewater.  For this purpose, micro-
particulate adsorbents were used along
with a Sep-Pak® precolumn for  rapid
trace enrichment. Identification of the
many chromatographic  peaks was
difficult, but the chromatograms  were
reproducible  and permit different ef-
fluents to be compared and  tertiary
treatment processes to be evaluated.
  This Project Summary was developed
by EPA's Health  Effects Research
Laboratory, Research Triangle Park.
NC, to announce key findings of the re-
search project that is fully documented
in a separate report of the same title (see
Project Report ordering information at
back).

Introduction
  The research  described  herein is  a
continuation of that reported in March
1979: EPA Report No. 600/1-79-014;
"Chemistry and Cytotoxicity of Renovated
Wastewater."  That report described a
method of analysis of filtered secondary
sewage-effluents using selective adsorp-
tion  and desorption of the less polar
organic constituents and yielded a
number of fractions of successively
decreasing polarity. These fractions were
tested for toxicity' by a micro-scale
cellular technique; some  tests of muta-
genic action were made, and  attempts
were made to  resolve the fractions into
individual, identifiable chemical com-
pounds.
  The primary  purpose of the continued
investigation, described in the final
report, was to study in  detail the
adsorptive properties of Bondapak-Cis®.
A secondary purpose was to determine
how this material, and others like it, could
be applied  to the  chromatographic
analysis of the organic compounds in
treated wastewater. The Bondapak-da®
adsorbent was chosen because, when
packed into a column, it retained an ap-
preciable proportion of the organic
material, about one-half of the total  or-
ganic carbon, and released nearly all of it
when water-methanol mixtures were
passed through the column.
  Bondapak-Cia® is a bonded-phase
adsorbent designed for large-scale or
preparative-scale liquid chromatography.
It consists  of irregular particles of
superficially porous silica,  size range 37-
75 micrometers, to  whose surface is
chemically bonded a  hydrocarbon layer,
equivalent to a coating of paraffin one-
molecule thick. The molecular fragments
bound to silica are  octadecyl groups,
Ci8H37. For  high-performance liquid
chromatography (HPLC) very small and
uniform particles, diameter  10 micro-
meters or less, are used, and  they are

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"totally  porous," that  is, they are
penetrated by internal channels and have
a large  effective surface area. Ideally,
every silicon atom on this surface carries
a carbon chain, if not  CisHs?, then CH3
groups used for "capping." The idea is to
prevent  free Si-OH  groups  that would
otherwise exist at the surface of silica. It
is  impossible  to avoid  Si-OH groups
entirely,  however, and  a part of the
surface of Bondapak-d8® may be con-
sidered to consist of Si-OH groups. They
change the adsorptive properties, making
the particles more prone  to adsorb polar
compounds,  and  even ionic compounds.
Chemically, the  coarse  Bondapak-Ci8®
closely resembles fine-particle  bonded-
phase adsorbents such as Micro Bonda-
pak-Cia® (Waters Associates), Partisil
ODS® (Whatman), and  Zorbax ODS®
(Dupont)*.

Experimental  Procedures

Model Solutes

Breakthrough  and
Elution  Studies
  Two kinds of tests were made: 1) break-
through, in which solutions of the organic
compounds were pumped through the
column  until  the  compounds "broke
through" the column and emerged at the
same concentration level  as they went in,
and 2) elution, in which small  portions
(0.1 ml or less) of solution were injected
into a flowing stream of solvent, and the
compounds were detected as a peak in
ultraviolet absorbance when they emerged.
"Elution" is the  normal  mode used in
chromatographic analysis, but "break-
through" and  its reverse, "stripping,"
provides  a better evaluation of the  be-
havior of the adsorbent in retaining trace
organic compounds from  water. Further,
"breakthrough" permits study of the ef-
fect of concentration and column loading.
  Benzophenone was  tested utilizing a
Bondapak-CiŁ(® column (0.45 cm ID x 10-
15  cm long).  Methanol-water mixtures
were pumped  through them  under
pressure, using  a Waters pump,  model
6000-A or 45; an ultraviolet absorbance
detector  operated at 254 nm  was con-
nected to the column exit. Methanol-
water mixtures were  used, rather than
pure water, because  benzophenone is
almost  insoluble in water; moreover,
retention times  in pure  water are ex-
tremely large.  Curves  for breakthrough,
stripping (desorption)  and elution of
benzophenone  in  50%  methanol  are
shown in Figure 1.
  Caffeine was also chosen for detailed
study because, as  a common contami-
nant  in wastewater,  it  is  sufficiently
hydrophobic to be adsorbed by Bondapak-
Cis®, yet is  freely soluble in water.
Adsorption-desorption  curves (Figure 2)
were obtained for caffeine at 10 ppm, in
simulated  city  water (distilled water
containing anhydrous CaSO.», 120 ppm;
NaHCO3, 70 ppm; and CaCI2 • 2H;>0, 47
ppm); on a Bondapak column (0.45 cm ID
x 5.5 cm long) that had been previously
conditioned with methanol.
  Other compounds selected for evalua-
tion were dibutylphthalate,  dioctyl-
phthalate,  2,4'-diachlorobiphenyl,  an-
thraquinone, pyrene, atrazine, 4,4'-
dichlorobiphenyl,  2,4-dichlorophenol,
furfural, and pentachlorophenol.  The
majority of  these compounds were
selected  from a  list of Consensus
Voluntary Reference Compounds (Keith
et a/., Environ. Sci. Tech., 13, 1469,
1979). These substances were passed
separately through a column of Bondapak-
Cis® (0.45  cm ID x 10.5 cm  long)  and
elution volumes, (Vei) measured. Most of
these substances are sparingly soluble in
water and are strongly retained; retention
volumes were therefore measured in
water-methanol mixtures.  Each mea-
         B s
   
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       Abs.
               100 mL
Figure 2.    Adsorption and desorption of caffeine on Bondapak-C^ from water. These curves
            are copied from strip-chart records. Caffeine concentration was 10 mg/L; flow rates,
            curve (a). 2.5 mL/min, 0.275 cm/sec; (b), 5.0 mL/min, 0.55 cm/sec; fcj,  7.5
            mL/min,  0.825 cm/sec.  Column dimensions, 0.45 cm x 5.5 cm. Absorbance
            measured at 280 nm, 1.0 absorbance units full scale. Note the small dependence on
            flow rate and the unsymmetrical shape, a nonlinear adsorbtion isotherm is
            indicated.
tubing with appropriate end fittings.
Columns were packed dry with Bondapak-
Cis®,  using  a  vibrator. Dry  packing  is
recommended by the manufacturer. Dry
packing is easier than slurry packing
(which was  also used) and gives equal
performance. Pure methanol was pumped
through the  packed columns to displace
air and render the packing hydrophilic.
Columns of different lengths and diame-
ters were used; the widest were 1.0 cm
ID;  most  were 0.45  cm ID.  The wall
thickness was 1 mm; end fittings were of
the standard "zero dead  volume" type
with stainless steel frits. Back pressures
were  of the order  of  100-500 psi  and
increased  with use.

Small-Scale Trace  Enrichment
  These experiments were conducted
using Sep-Pak® (small disposable cart-
ridge  packed with  a  micro particulate
bonded adsorbent — Waters Associates)
for preconcentration. The procedure was
as follows:
  a) Sample  preparation. Filter  a quantity
(50-200 ml) of secondary sewage effluent
through Whatman glass-fiber filter
paper, grade GF/F, adjusting the pH with
nitric acid  where desired. Next, condition
the Cie  Sep-Pak® by passing 2  ml
methylene chloride followed by 5 ml of
methanol. Attach the Sep-Pak® to a Luer
tip syringe and drive the filtered waste-
water through the Sep-Pak® at 5 ml/min
using  a  Sage pumping assembly or
equivalent. Now displace as much water
as possible by  passing  50  ml  of air
downwards thru  the column.  Evaporate
the methylene chloride just to dryness
using a stream of nitrogen. Dissolve the
residue in 0.1-0.15  ml methanol and add
1 ml of water.
  b) Sample introduction-liquid chromat-
ograph. A  liquid chromatography as-
sembly consisting of two Water Model
6000A pumps (Waters Associates),  a
Model 660  solvent  programmer (Waters
Associates),  a U6K injector (Waters
Associates), a Valco six-port valve,  a
Whatman PXS-ODS analytical  column, a
Brownlee precolumn, a  Schoeffel vari-
able-wavelength  ultraviolet detector and
a Schoeffel fluorescence detector with a
Linear Instruments two-pen recorder
was used. The valving system allows one
to inject a fairly large sample, up to 2 ml,
which is the volume of the storage loop of
the U6K injector, and collect the dissolved
compounds on the Brownlee precolumn;
then,  by passing  a  higher concentration
of methanol and reversing the  solvent
 flow, the various dissolved compounds
 are focused  so that they enter the
 analytical column together  in  a  small
 volume.

 Results and Discussion

 Adsorptive Properties of
 Bondapak-C^a

 The Adsorbent
   Regarding chemical  selectivity, the
 partition  of pure organic compounds
 between  the  adsorbent  and a solvent
 (water or methanol-water mixture) and
 the order in which a series of compounds
 is adsorbed and released are the same for
 the 37-75 micron Bondapak-de® as the
 fine particle (< 10 micron) Cis bonded
 phases used in HPLC. The main advant-
 ages of  Bondapak-Cia® for wastewater
 analysis  and the preparation of fractions
 for toxicity testing are  that it  is  more
 robust and less prone to fouling by humic
 substances,  and  back pressures are
 much less than those observed with 10-
 micron particles,  and the material  is
 considerably less expensive.
   When  using Bondapak-Cis® to adsorb
 organic compounds from water, it must
 be recognized that it is hydrophobic and
 not wetted  by water. It must first be
 thoroughly wetted with at least 50%
 methanol or  another water-miscible
 solvent; then,  when the greater part of
 this solvent has been washed out, the
 absorbent can  be used to take up organic
 compounds from  water. Its behavior
 towards purely aqueous solutions depends
 strongly on the small amounts of methanol
 sticking to it, and inevitable the behavior
 is unreproducible, making it impractical
 to try to characterize it by exact physical
 tests. In mixed water-methanol solvents,
 however, its behavior is reproducible and
 similar to that of  microparticulate -Cis
 bonded packings, except for the lower
 plate numbers.

 Model Solutes
  Experimental values of Vads, volume of
 desorption (Vdes), and  Vei for benzophe-
 none; listed in Table 1, indicate that the
 adsorption of benzophenone on Bonda-
 pak-Cie follows a linear  isotherm. As-
 suming the isotherm to be linear, even at
 lowest concentrations, one can predict
 that the breakthrough volume, Vads, is the
 same at  the very low concentrations
 prevailing in treated  sewage effluents
 and in polluted water  as  it is using the
concentrations in this work.
  Figure 2 shows the adsorption-desorp-
tion curves for caffeine. A  marked
contrast exists between these curves and

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I

.O
I
Qi
O
-J
      1.5
1.0
      0.5
                                           Benzophenone
                                                               2.5
                                                               2.0
                                                                      1.5
                                                                      1.0
                  W
                            20        30        40

                             Volume Percent Methanol
                                                    50
Figure 3.
     Adsorption (breakthrough) of furfural and bemophenone on Bondapak-Cia versus
     volume fraction of methanol. Furfural column was 0.45 cm x 10.5 cm, void volume
     0.8 mL; bemophenone column was 0.32 cm x 11.6 cm, void volume 0.6 mi-
     Adsorption volumes are in mL, corrected for the void volume.
those shown in Figure 1 for benzophenone.
In Figure 2, there is a rapid concentration
rise during  breakthrough and a slower
concentration  fall during stripping. This
behavior is due to a nonlinear adsorption
isotherm. When  nonlinear adsorption
occurs, the adsorption becomes less
strong as the concentration rises; this is a
common phenomenon in chromatography.
Measurements of Vads at different con-
centrations confirms this interpretation;
as shown in Table 2.
   Breakthrough volumes were measured
for furfural  at methanol concentrations
ranging from  50% to 20% and in pure
water. Figure  3 shows the relationship.
At low methanol concentrations,  the
linear  relationship breaks down. Adsorp-
tion on hydrophobic bonded-phase adsor-
bents is stronger in pure water and at very
low methanol concentrations than  the
straightline plots predict.  It  has been
suggested that in solvents  rich in
methanol, the long  bonded hydrocarbon
chains stretch out into  the solvent  and
move freely about their anchor points on
the silica surface, but irr pure water they
stick to each  other to form a compact,
hydrophobic, matted layer.
                                    Data for the other model solutes (Figure
                                  4) suggests a linear isotherm, however,
                                  the limited number of points makes it
                                  impossible  to  determine  if a linear
                                  relationship holds at  low methanol
                                  concentrations or whether an effect
                                  similar  to  that  observed for furfural
                                  occurs.

                                  Wastewater Studies

                                  Large Scale Trace  Enrichment
                                  with Gradient Elution
                                    FigureB shows the results of tests with
                                  two Bondapak-da® columns. The erratic
                                  rise  and fall of the dissolved TOC was
                                  mainly  attributed to the  inability to
                                  maintain  a  consistent  flow rate. The
                                  effect of pH is clearly seen. Sorption was
                                  more effective at lower  pH  as expected
                                  since undissociated acids (mainly humic
                                  acids) are more strongly retained than the
                                  acid anions.
                                    With  the larger column, the TOC falls
                                  as  more liquid is passed.  At the very
                                  beginning of a run, the TOC is abnormally
                                  high due to methanol that is washed out
                                  of the adsorbent, but this effect only lasts
                                  for 100 mL. at most. The gradual fall in
TOC seen in Figure 5 might be due to
another effect. Perhaps the humic acid
adsorbed on the Bondapak-Cia® enhances
the adsorption of other organic com-
pounds. With the small column, however,
the TOC rises slowly, that is,  sorption
becomes less efficient as time goes on.
This is a more understandable effect, for
the column  must eventually  become
saturated with adsorbed material. Curve
(d), Figure 5, shows that the column had
adsorbed 6 mg of  organic carbon during
the run. The dry weight of Bondapak-Cia®
in this column was 0.7 gram.

Small-Scale Trace Enrichment
  A serious  difficulty in analyzing the
potentially toxic trace organic compounds
in treated sewage isolated by the above
procedure  is the presence of  humic
material. Humic material is not a single
chemical substance but an  ill-defined
high  molecular weight  polyelectrolyte
with  a  variety of  functional groups. By
utilizing a" Ci8 Sep-Pak® that has been
conditioned  with  methanol, the  humic
material is held back as a thin brown ring
at the entrance to the Sep-Pak®. Elution
with methylene chloride leaves nearly all
the humic material behind. Despite this
separation, the identification of individual
peaks is nearly impossible because of
their  number and  peak overlap. However,
portions of the same filtered waste water
passed through different Sep-Paks® and
analyzed separately produced essentially
identical chromatograms. Figure 6 shows
the fluorescence record for a Denver and
a Boulder wastewater. Note the prominent
peaks in the Boulder sample.

Conclusions
   Bondapak-Cia® adsorbs relatively
hydrophobic compounds, including caf-
feine, phenols and chlorophenols, most
pesticides,  plasticizers  and polycyclic
aromatic hydrocarbons.
   The main advantages of Bondapak-Cia
(37-75 microns)  over microparticulate
Bondapak-Cia (less than 10 microns) for
wastewater analysis and the preparation
of fractions for toxicity  testing are: its
lower cost and the fact that it is more
robust  and less prone to fouling by the
humic substances.
   Adsorption and retention volumes
were determined for a variety of model
solutes. These values were not affected
appreciably by levels of salts and humic
 substances  normally  encountered  in
 drinking water.
   Preliminary data are given on a method
 of HPLC that uses a Sep-Pak® to adsorb
 and  separate the less polar organic

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Figure 4.
                                30      40      50      60

                                Volume Percent Methanol
Plots of capacity factors versus methanol concentration Bondapak-C^. Column
(0.45 cm ID x 10.5 cm long); void volume 0.6 mL; to find the adsorption volumes in
ml, add (log 0.6 = -0.221 to ordinates.
                                 compounds  from  water and humic
                                 material.

                                 Recommendations
                                   Two practical purposes remain to be
                                 fully realized: one is the separation of the
                                 dissolved organic material in wastewater
                                 and treated sewage into well-character-
                                 ized  fractions,  with a view  to toxicity
                                 testing, and  the  other is the chemical
                                 analysis and recognition of  specific
                                 organic compounds, including nonvolatile
                                 compounds,  by high-resolution liquid
                                 chromatography. This work advanced
                                 significantly  toward this goal  through
                                 Sep-Pak®  trace  enrichment and high
                                 resolution  liquid chromatography, as
                                 described  in  the  latter part of the final
                                 report. These  efforts should be continued,
                                 with emphasis  on selective methods of
                                 chromatographic  detection,  particularly
                                 electrochemical, which distinguish oxidi-
                                 zable  compounds like  phenols  and
                                 benzidines. Electrochemical  techniques
                                 are now possible  that can be used with
                                 gradient elution, which the older tech-
                                 niques could  not.
                                   A  few tests  were  made  with other
                                 adsorbents,  notably anion-exchange
                                 resins, Duolit*  A-7 and Bio-Rad MP-1.
                                 Those resins removed organic compounds
                                 from water that were not removed by
                                 Bondapak-Cis®. Stripping  each sorbent
                                 in turn using pH  and solvent gradients
                                 would permit further selective fractiona-
                                 tion.  Additional work is needed in  this
                                 area.
'able 1.    Adsorption and Desorption Volumes of Benzophenone on Bondapak-C\a from Solu-
          tions in 50% Methanol (V/V)
Benzophenone
  concentration, ppm:
                     0.5
2.5
5.0
                                                             6.5
c/ow rate, mL/min:
/ads (mL):
/des* (mL):
1.0 0.5
9.6 9.9
9.6 9.9
0.5
9.9. 9.9
10.2. 9.0
9.9, 9.9
9.8, 9.8
0.5
9.9
9.8
0.5
9.9, 9.8
9.8
9.8, 9.8
9.8
NOTES: (a)column dimensions, 0.45 cm x 10.5 cm.

       (b) theoretical-plate numbers, from adsorption and desorption profiles, 115(1 mL/min),
         165 (0.5 mL/min).

       (c)elution volumes, Vei, for injections of benzophenone varying between 0.2 and 5.0
         micrograms. were 10.0 ± 0.05 mL (mean of 14 measurements).
*Vaes - stripping or desorption volume.

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Table2.    Adsorption Volumes of Caffeine on Bondapak-Cie from Water
Caffeine concentration, ppm:
Adsorption volume, mL,
  at flow rates:
                              2.5 mL/min
                              5.0 mL/min
                              9.9 mL/min
70
65
63
2.5
71
62
56
10
48
46
42
Column (0.45 cm ID x 10 cm long), freshly packed.
  I

         10
  I
  13
                                                              (a)
\
                           1000
                                                       2000
        10
                                                                           (d)
                                                                               Figure 6.    Fluorescence Chromatograms
                                                                                           of two secondary sewage efflu-
                                                                                           ents; (a) Boulder, (b)  Denver.
                                                                                           Each injection corresponds to 10
                                                                                           mL  of secondary effluent. Sol-
                                                                                           vent gradient went from 25% to
                                                                                           75% methanol in 40 minutes.
                                     500
                                                       1000
                                       mL Effluent

Figure 5.    Dissolved organic carbon in effluent from Bondapak- Ci e- Curves (a) and(c), column 1
             cm x 1O cm; influent, 19.5 ppm carbon; (a), pH 7.2; (c), pH 3.5. Curve (b). column
             1 cm x10 cm; influent, 17 ppm carbon; pH 7.5. Curve (b) was taken a month after (a)
             andfc) but with the same packed column. Flow rate was about 5 mL/min but could
             not be controlled accurately. Points (d), column 0.45 cm x 10 cm; influent, 14 ppm
             carbon, pH 7.5; flow rate, 1.5 mL/min.
                                                                         &U. S. GOVERNMENT PRINTING OFFICE: 1985/559-111/10765

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Harold F. Walton is with the University of Colorado, Boulder. CO 8030 J.
H. P. Ringhand is the EPA Project Officer (see below).
The complete report, entitled "Sorption Properties of Model Compounds on Ci8
  Adsorbents, "(Order No. PB 85-125 839; Cost: $8.50, 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:
        Health Effects Research Laboratory
        U.S. Environmental Protection Agency
        Research Triangle Park, NC 27711

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Harold F. Walton is with the University of Colorado, Boulder, CO 80301.
H. P. Ringhand is the EPA Project Officer (see below).
The complete report, entitled "Sorption Properties of Model Compounds on Ci$
  Adsorbents, "(Order No. PB 85-125 839; Cost: $8.50, 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:
        Health Effects Research Laboratory
        U.S. Environmental Protection Agency
        Research Triangle Park. NC 27711

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      HaroldF. Walton is with the University of Colorado. Boulder. CO 80301.
      H. P. Ringhand is the EPA Project Officer (see below).
      The complete report, entitled "Sorption Properties of Model Compounds on Cia
        A dsorbents." (Order No. PB85-125 839; Cost: $8.50, 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:
             Health Effects Research Laboratory
             U.S. Environmental Protection Agency
             Research Triangle Park, NC 27711
United States
Environmental Protection
Agency
Center for Environmental Research
Information
Cincinnati OH 45268
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