Chemical
Oceanography Div.
Korea Ocean Research & Development
Institute
Ansan
e-mail:
jroh@kordi.re.kr
Alkylphenol ethoxylates(APEs), chlorophenols(CPs) and bisphenol-A(BPA) have
been widely used in the preparation of detergents, wood preservatives and
polymeric materials for household and industrial applications. They have been discharged directly or indirectly
to environment, and contaminated the atmosphere, water and soil. APEs are degraded
to alkylphenols(APs) during
aerobic or anaerobic waste treatment process or by micro-organism and
photolysis in the nature. Although the APEs are less toxic to organism, their metabolites show
high toxicity to organisms. So most countries including
Phthalates
have a broad range of applications.
Phthalate esters are liquid plasticizers, similar in appearance to
vegetable oils, which are added to a hard plastic called polyvinyl chloride
(PVC or vinyl). The liquid phthalates
act as a softener causing the PVC, which is hard in its raw form, to become flexible.
Phthalates have made possible a wide range of flexible vinyl products which
have improved the quality of life in homes, offices and hospitals for more than
several tens years, including vinyl wall covering flooring, upholstery, wire
and cable sheathing, medical products, packaging and toys. Unplasticized
PVC is hard it might be used in such applications as piping or plumbing
fixtures. Phthalates may also be used to
lubricate and/or enhance the durability and longevity of other materials. Such applications include detergents,
solvents, lubricating oils and personal care products, such as lotions, nail
polish, perfumes and pharmaceuticals(http://www.phthalates.org/html/pegenhow.htm). Phthalates exhibit very low direct acute toxicity.
However, long time exposure has shown toxic effects on testes, kidney and liver
in animal experiments.
Table
1 shows the target analytes of phenolic
compounds, phthalates and organochlorine pesticides.
|
Phenols(11) |
Phthalates(9) |
Pesticides(10) |
|
t-butylphenol(t-BP) |
diethylphthalate(DEP) |
a-HCH |
|
n-butylphenol(t-BP) |
dipropylphthalate(DprP) |
b-HCH |
|
n-pentylphenol(n-PP) |
dibutylphthalate(DBP) |
g-HCH |
|
n-hexylphenol(n-HexP) |
dipentylphthalate(DPP) |
d-HCH |
|
n-heptylphenol(n-HepP) |
butylbenaylphthalate(BBP) |
p,p-DDD |
|
t-octylphenol(t-OP) |
dihexylphthalate(DHexP) |
p,p-DDE |
|
n-octylphenol(n-OP) |
dicycrohexylphthalate(DCHP) |
p,p-DDT |
|
nonylphenol(NP) |
diethylhexyladipate(DEHA) |
aldrin |
|
2,4-dichlorophenol(DCP) |
diethylhexylphthalate(DEHP) |
dieldrin |
|
pentachlorophenol(PCP) |
|
endrin |
|
bisphenol-A |
|
|
Water
samples were collected by using pre-cleaned one liter amber glass bottles with teflon-lined caps.
Duplicate samples were collected from each sampling sites. The sampling personnel wore latex gloves
during sampling. The personnel put the
bottle under the surface of the water as it is closed and open it till it
becomes a half full. Close the bottle
and take it out. Shake the bottle 10
seconds and discard water from the bottle.
Put the bottle under the surface of the water as it is closed again and
open it till it becomes full. Close the
bottle and take it out. Open the cap and
add surrogate standards to the sample.
Store the sample in the room temperature and ship back to the laboratory
as soon as possible. If it is not
possible to analyze the sample immediately, extract the sample with solvent.
Coastal
water sampling sites were selected according to the following criteria:
· The site shall be outside
the zone of initial dilution of a dumpsite or point-source discharge, and easy
to access
· The sampling sites will coincide with historical monitoring sites (i.e., on-going Korea Ministry of Environment Endocrine Disruptors Monitoring Program) when feasible and all other criteria are met.
Sampling
sites of coastal seawater is shown in Fig. 1.
The
weather was fine during water sampling in September, 2001 and January,
2002. Most sampling dates in September
were sunny and air temperature was quite hot.
Sampling dates in January were sunny and no snowing during sampling
period.
All
the samples were analyzed by using Shimadzu GC-MS QP5000.
Organochlorine pesticides in water
Not
like 1999 and 2000, all the surficial waters were
below detection of organochlorine pesticides in
summer and winter.
The
total phenolic compounds concentrations ranged from
60 to 285 ng/L (Table 3). In our samples, the most abundant phenolic compounds were Nonylphenol
and Bisphenol-A. Nonylphenol
was detected in all samples.
4-t-Butylphenol was present in 8 samples out of 9. t-Ocytlphenol was
present in 7 samples out of 9.
4-n-Butylphenol, n-Pentylphenol,
4-n-Hexylphenol, n-Heptylphenol and n-Octylphenol were not detected at all. The total alkylphenol
concentrations ranged from 46 (Uljin) to 182 ng/L (
Chlorophenols were not detected at all.
Bisphenol A was detected in all samples.
The concentrations ranged from 14 (Uljin) to
137 ng/L (
The
total phenolic compounds concentrations ranged from
31 to 1736 ng/L (Table 4). The most abundant phenolic
compound was nonylphenol like summer. 4-t-Butylphenol t-Octylphenol
were present in 8 samples out of 9. Nonylphenol and Bisphenol A were
detected in all samples.
4-n-Butylphenol, n-Pentylphenol, 4-n-Hexylphenol,
n-Heptylphenol and n-Octylphenol
were not detected at all. The total alkylphenol concentrations ranged from 18 (Uljin) to 1392 ng/L (Busan). Busan showed extremely high level of Nonylphenol. The alkylphenols
concentrations were generally lower than summer except Busan
and
Chlorophenols were not detected at all.
Bisphenol A was detected in all samples.
The concentrations ranged from 12 (Shiwha) to
344 ng/L (Busan). Busan and
The
total phthalates concentrations ranged from undetected to 246 ng/L (Table 6). In
our samples, the most abundant phthalates compounds were DBP and DEHP. DBP was present in 5 samples out of 8 and
DEHP was present in 7 samples out of 8. DEP, DprP,
DPP, BBP, DhexP, DCHP and DEHA were not detected at
all. DBP concentrations ranged from
undetected to 59 ng/L. DEHP concentrations ranged from undetected to
311 ng/L. The
level of DEHP was generally much higher than DBP.
The
total phthalates concentrations ranged from 17 to 304 ng/L
(Table 7). Like summer, the most
abundant phthalate compounds were DBP and DEHP.
DBP was present in 5 samples out of 9 and DEHP was present in 9 samples
out of 9. DEP, DprP,
DPP, BBP, DhexP, DCHP and DEHA were not detected at
all. DBP concentrations ranged from
undetected to 122 ng/L. DEHP concentrations ranged from 17 to 182 ng/L. Like summer,
all sites showed higher level of DEHP than DBP except
A
five-point calibration curve established the response of the detector. The calibration curve was prepared using a
linear calibration equation. The
calibration solutions were analyzed in the beginning and at the end of the
analytical GC-MS run.
An
acceptable method blank analysis did not contain any target compound at a
concentration 3 times greater than the MDL (Table 8). If the method blank did not meet these
criteria, the analytical system was out of control and the source of the
contamination was investigated and corrective measures taken and documented
before further sample analysis proceeded.
For
organochlorine pesticides analysis, phenanthrene-d10
and perylene-d12 were used as internal standards. For phenolic
compounds, bisphenol A-d14 was used as surrograte standard, and naphthalene-d8, phenanthrene-d10 and
perylene-d12 were used as internal standards.
For phthalates, Di n-butyl phthalate-d4
(DBP-d4), Di 2-ethylhexyl phthalate-d4 (DEHP-d4) were
used as internal standards, and Di n-pentyl phthalate-d4(DPeP-d4) was used as surrogate
standard. The internal and/or surrogate
standard solution was spiked into the sample prior to extraction in an attempt
to compensate for individual sample matrix effects associated with sample
preparation and analysis. The laboratory
took corrective action whenever the recovery of the internal standard used to quantitate was outside of the 60 to 140% range. The following corrective action was taken
when an out of control event occurred:
Calculations
were checked to assure that no errors were made. The internal standard solutions were checked
for degradation, contamination, and other problems, and instrument performance
was checked. If the steps above failed
to reveal a problem, the sample or extract was reanalyzed. If reanalysis of the extract yielded internal
standard recoveries within the stated limits, then the reanalysis data was
reported. If QA criteria were still
violated upon reinjection, the sample was submitted
for re-extraction.
The
target compounds, internal standard, and GC internal standard were resolved
from one another and from interfering compounds. When they were not, coelutions
were documented.
Recovery and
Reappearance Test
10 ng of each phthalate was added into seven real water samples (100 ml) and took the same preparation and analysis to check the recovery. The recovery of phthalates showed very good result and range was 96.4~121.7%(Table 9 & 10). CV was 4.2~13.7%.
2 ul of each phthalates standards (0.200ng/ml) were analyzed
seven times by using GC-MS to check the repeatability
of analysis (Table 11). It showed excellent
repeatability of analysis and range was 0.197~0.229 ng/ml. CV was from 1.0 to 4.8% except BBP (11.7%).
Sediment
CRM (CRM117-100) was purchased from R.T. Cooperation and analyzed for
phthalates (DEP, DBP and DEHP). CRM was
analyzed 10 times. The results should
agree within 65 to 135% of certified values.
The average of recovery of DEP was 113% and range was 72~128%(Table 12). The average of recovery of DBP was 103% and
range was 67~133%. The average of recovery of DEHP was 107% and
range was 70~130%. All the results were within 65 to 135% of
certified values.
Because
of aging of GC-MS, it has been out of order frequently and it hindered routine
maintenance of the instrument. The PC
attached to GC-MS is an old model, so its speed is too slow to proper
treatment of chromatograms. It can be
easily mended by changing the old PC.
No organochlorine
pesticides and chlorophenols were detected in this
study.
Alkylphenols and bisphenol-A were detected in summer and winter. The range of alkylphenols in summer and winter were 25~142 ng/L and 18~1392 ng/L respectively. 4-t-Butylphenol and Nonylphenol were dominant compounds among target alkylphenols. The range of bisphenol-A in summer and winter were 14~137 ng/L and 12~344 ng/L respectively.
The level of total phenolic
compounds was generally higher in summer than winter except Busan
and
The level of bisphenol A showed very similar trend to total phenols. The level was generally higher in summer than
winter except Busan and
Only
DBP and DEHP were detected among 11 target phthalates in summer and
winter. DEHP level was generally higher
than DBP level in summer and winter (Fig. 7 & 8). There was no special seasonal variation of
DBP levels (Fig. 9). But DEHP level in
summer was generally higher than in winter except Uljin
(Fig. 10).

Fig. 1. Sampling sites of seawater

Fig. 2. Seasonal variation of phenolic compounds in seawater

Fig. 3. Comparison between alkylphenols and bisphenol-A in summer
Fig. 4. Comparison between alkylphenols and bisphenol-A in winter
Fig. 5. Seasonal variation of alkylphenols in seawater

Fig. 6. Seasonal variation of Bisphenol A in seawater

Fig. 7. Comparison between DBP and DEHP in summer

Fig. 8. Comparison between DBP and DEHP in winter

Fig. 9. Seasonal variation of DBP in seawater

Fig. 10. Seasonal variation of DEHP in seawater
Table
2. Concentrations of organochlorine pesticides from
seawater in summer (ng/L)
|
Compounds |
Uljin |
|
|
Busan |
|
|
Kunsan |
Boryung |
Shihwa |
|
a"-HCH |
ND |
ND |
ND |
ND |
ND |
ND |
ND |
ND |
ND |
|
b-HCH |
ND |
ND |
ND |
ND |
ND |
ND |
ND |
ND |
ND |
|
g-HCH |
ND |
ND |
ND |
ND |
ND |
ND |
ND |
ND |
ND |
|
d-HCH |
ND |
ND |
ND |
ND |
ND |
ND |
ND |
ND |
ND |
|
Aldrine |
ND |
ND |
ND |
ND |
ND |
ND |
ND |
ND |
ND |
|
Dieldrine |
ND |
ND |
ND |
ND |
ND |
ND |
ND |
ND |
ND |
|
Endrin |
ND |
ND |
ND |
ND |
ND |
ND |
ND |
ND |
ND |
|
p,p'-DDE |
ND |
ND |
ND |
ND |
ND |
ND |
ND |
ND |
ND |
|
p,p'-DDD |
ND |
ND |
ND |
ND |
ND |
ND |
ND |
ND |
ND |
|
p,p'-DDT |
ND |
ND |
ND |
ND |
ND |
ND |
ND |
ND |
ND |
|
Total |
ND |
ND |
ND |
ND |
ND |
ND |
ND |
ND |
ND |
Table
3. Concentrations of organochlorine pesticides from
seawater in winter (ng/L)
|
Compounds |
Uljin |
|
|
Busan |