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Use of PAHs in Environmental
Forensics
Presented by:
Court Sandau, PhD, PChem
ISPAC 2013
Corvallis, OR
Environmental Forensics
• What is it?
• Analytical issues with PAHs and EFI
• Expanding PAHs (beyond 16)
• PAHs and EFIs – examples and case
studies
2
For case study on PAHs and a pipeline oil spill, see a part blog on our website:
http://chemistry-matters.com/pipeline-spill/
For more information on PAHs, click here to see our website page on PAHs.
Environmental Forensic Investigation
The systematic examination of historical and
environmental information (which may be used in
litigation) to allocate responsibility for contamination
“The application of
scientific methods used to
identify the origin and
timing of a contaminant
release”
See our website for more information on environmental forensic investigations.
Disciplines in Environmental Forensics
• Chemistry
• Statistics
• Engineering
• Microbiology
• Hydrogeology
• Soil Science
• Toxicology
• Biology
• Ecology
• Litigation Experience
• And others….
Birthplace of Environmental Forensics
Exxon Valdez 1989
Term “Environmental Forensics”
coined in Dr. Robert Morrison’s
first books since it was used in a
peer reviewed publication. 5
Crime Scene Investigations
6
Environmental Forensic Investigation
EFI Video
Click here for link to video on slideshare.
Two Categories of EFIs
Academic & Research
Liability Driven
Litigation and Liability Driven EFIs
• Adversarial process
• Goal – make you look bad or incompetent while making
themselves look good/sympathetic
• They are trying to tell if you are telling the truth or not
• Good science does not necessarily prevail
• Unfortunately, science is complicated (scientific literacy
28% in 2007)
• Need to prove it beyond a reasonable doubt
10
Differences Between Legal and
Research
• Documentation,
Documentation,
Documentation
Project id.
Address
Project id.DateDate
Date
Notes and pictures/videos
Differences Between Legal and
Research
• Documentation
• Sample Handling
• Chain of Custody
Differences Between Legal and
Research
• Documentation
• Sample Handling
• Chain of Custody
• Laboratory Competence
• Standard Procedures
• Communicating Results
Carpet Dust Sampling
• Must follow
standardized
procedures where
available
• Difficult to change
approaches
• Validation required if
methodology changes
Designation: D 5438 – 05
Standard Practice for
Collection of Floor Dust for Chemical Analysis1
This standard is issued under the fixed designation D 5438; the number immediately following the desig
original adoption or, in the case of revision, the year of last revision. A number in parentheses indicates th
superscript epsilon (e) indicates an editorial change since the last revision or reapproval.
1. Scope
1.1 This practice covers a procedure for the collection of a
sample of dust from carpets and bare floors that can be
analyzed for lead, pesticides, or other chemical compounds and
elements.
1.2 This practice is applicable to a variety of carpeted and
bare floor surfaces. It has been tested for level loop and plush
pile carpets and bare wood floors, specifically.
1.3 This practice is not intended for the collection and
evaluation of dust for the presence of asbestos fibers.
1.4 The values stated in SI units are to be regarded as the
standard.
1.5 This standard does not purport to address all of the
safety concerns, if any, associated with its use. It is the
responsibility of the user of this standard to establish appro-
priate safety and health practices and determine the applica-
bility of regulatory limitations prior to use.
2. Referenced Documents
2.1 ASTM Standards: 2
D 422 Test Method for Particle-Size Analysis of Soils
D 1356 Terminology Relating to Sampling and Analysis of
Atmospheres
E 1 Specification for ASTM Thermometers
E 337 Test Method for Measuring Humidity with a Psy-
larger, embedded in carpet
household vacuum cleaners
3.1.2 surface dust—soil
proximately 5-µm equivalen
adhering to floor surfaces a
hold vacuum cleaners.
4. Summary of Practice
4.1 The sampling metho
from work published in Rob
(4).
4.2 Particulate matter is
floor by means of vacuu
through a sampling nozzle
and the particles are separat
cyclone is designed to effic
approximately 5-µm mean
However, much smaller par
efficiencies. The sampling
and suction adjustments to
air velocity for the removal
and bare floor surfaces, so
be repeated.
NOTE 1—Side-by-side compa
upright vacuum cleaner revealed
Designation: D 422 – 63 (Reapproved 2002)e 1
Standard Test Method for
Particle-Size Analysis of Soils1
This standard is issued under the fixed designation D 422; the number immediately following the designation indicates the year of
original adoption or, in the case of revision, the year of last revision. A number in parentheses indicates the year of last reapproval. A
superscript epsilon (e) indicates an editorial change since the last revision or reapproval.
HVS-3 Vacuum Cleaner
Commercial Laboratory
PAH Analysis
• Methods vary from lab to lab
• Quantification
– Semi-quantitative methods with surrogates
– Quantitative methods with labeled internal
standards
• Analytes measured
– Routine EPA
– Routine EPA+
– Deluxe EPA compounds with substituted PAHs
and then some (up to 63 compounds in an
analysis)
www.chemistry-matters.com 16
US EPA Priority Pollutants
PAH Compounds
benzo[k]fluoranthene benzo[a]pyrene
benzo[b]fluoranthenepyrenefluoranthenechrysene
fluorenephenanthreneacenaphthyleneanthraceneacenaphthenenaphthalene
benzo[ghi]perylenedibenz[a,h]anthracene indeno[1,2,3-cd]pyrene
benzo[a]anthracene
2-ring 3-ring
4-ring
5-ring 6-ring
LMW
HMW
Analysis of PAHs
S
Retention Time
RelativeResponse
Interlaboratory Comparisons
Method 8270C
• Interlaboratory study conducted
• Each lab measured homogeneous
soil sample 4 times over a ~ week
• Requested standard PAH method
• Compared variability amoung labs
and within each laboratory
Naphthalene
Fluorene
Pyrene
0.00
0.10
0.20
0.30
0.40
0.50
0.60
0.70
0.80
0.90
All Labs Lab A Lab B Lab C Lab D Lab E Lab F Lab G Lab H
mg/kg
Mean Value Maximum Value Minimum Value
FAL - Coarse (0.40)
Results
• Laboratory variability issues amoung
laboratories
• Sample to sample variability within
the laboratories
Variability can be measured and controlled with
a good data validation program
Method Comparison - PAHs
Low Resolution MS Method
• EPA Method 8270C
• Full Scan analysis
• No confirmation ions or
ratios
• Inappropriate surrogate
standards
• Many versions of method
High Resolution MS Method
• Modified California Method
(Carb 429)
• IDMS quantitation
• Less likely to have
interferences present
• Isotopically labeled
standards
• More accurate and precise
• Better data = better
decisions
PAH Analysis
• Many interferences exist in low molecular
weight range
– Depends on matrix, clean up method
• Specificity of HRMS allows better accuracy
and precision
• Comes at a cost – 4-6x
Difference in measuring
252 versus 252.30928
Benzo(a)pyrene
Internal Standards vs. Surrogates
naphthalene phenanthrene benzo(a)pyrene
N+
O
O-
F
*
*
*
*
*
*13
C
*
* *
*
**
* *
*
*
Isotope Dilution Quantification
• Standards behave exactly like compounds
being analyzed
• Loss of analytes during method, included
in measurement
• Matrix interferences in method, can usually
be seen with standards as well
• THE most accurate measurement
available
Is more expensive better?
Experiment:
• SRM – determine accuracy
• Duplicate – determine precision
• Unknown duplicates to compare
results
Compared methods, not laboratories
Lab A – ID-HRMS
Lab B- LRMS, surrogates
PAH Comparisons
0
0.2
0.4
0.6
0.8
1
1.2
AcenaphtheneAcenaphthylene
Anthracene
Benzo(a)anthraceneBenzo(a)pyrene
Benzo(b)fluoranthene
Benzo(g,h,i)perylene
Benzo(k)fluoranthene
Chrysene
Dibenz(a.h)anthracene
Fluoranthene
Fluorene
Indeno(1,2.3-cd)pyrene
2-Methylnaphthalene
Naphthalene
Phenanthrene
Pyrene
Certified SRM Value Lab A Lab B
Compound
Concentration(ng/g)
Standard Reference Material
Overestimation
PAH Duplicate Results
0
20
40
60
80
100
120
BaA BaP BbF BkF CHRY FLUOR PHEN PYR
Sample 1 Sample 2
0
20
40
60
80
100
120
BaA BaP BbF BkF CHRY FLUOR PHEN PYR
Sample 1 Sample 2
Compounds
Compounds
Concentration
(ng/g)
Concentration
(ng/g)
Lab B
Lab A
100% 92% 111% 100% 86% 94% 101% 90% RPD
3% 8% 15% 16% 18% 17% 27% 11% RPD
0
5000
10000
15000
20000
25000
30000
35000
ACE
ACY
NAP
2-NAP
FLR
ANT
PHEN
FLUOR
PYR
BAA
CHRY
BBF
BKF
BAP
B(ghi)P
DB(ah)A
IND
0
100
200
300
400
500
600
700
800
900
1000
ACE
ACY
NAP
2-NAP
FLR
ANT
PHEN
FLUOR
PYR
BAA
CHRY
BBF
BKF
BAP
B(ghi)P
DB(ah)A
IND
Results of On-Site Samples (unknowns)
LRMS Method
HRMS Method
Causes of Overestimation
• Incomplete cleanup, residue matrix in
extracts
• Co-elution of other PAHs not being
monitored
Data Quality for PAHs
• Low resolution surrogate MS methods for
PAHs can be highly variable between
laboratories
• Sites driven by PAH risk require IDMS
– Sensitivity – for the guidelines
– Specificity – for the interferences that are
naturally present in samples
• IDMS methods are suggested for forensics
investigations
– May reduce variability of diagnostic ratios
Diagnostic Ratios
Ratios Values / Sources References
Phenanthrene /
Anthracene
< 5 = Pyrogenic; > 5 =
Petrogenic
Neff et al., 2005
Fluorene / Pyrene
+ 1 = Pyrogenic. < 1 =
Petrogenic
Neff et al., 2005
Indeno(1,2,3-cd)pyrene /
(Indeno(1,2,3-cd)pyrene
+ Benzo(g,h,i)perylene
> 0.1 = Combustion
Motelay-Massei et al
2007; Yunker et al.,
2002
Fluoranthrene/ Pyrene
< 1 = Petrogenic; >1
Pyrogenic
Motelay-Massei et al
2007
LMW / HMW < 1 = Combustion Zhang et al 2005;
Benzo(a)pyrene /
Benzo(a)pyrene +
Chrysene
< 0.2 = Petrogenic; >
0.35 = Combustion
Zhang et al 2005;
Zhang et al 2007
• Decrease analytical variability with better methods
• Some good, some not as good – use what fits?
• Good for bulk characterization – what about further
distinction of sources
Expanding the List of PAHs
Alkylated-PAHs and Other PAHs
C1-Phenanthrenes
1
2
3456
7
8
9 10
CH3
C2-Phenanthrenes
Phenanthrene
CH3
CH3
CH3
H3C
CH2 CH3
C3-Phenanthrenes
C4-Phenanthrenes… (?)
CH3
CH3
CH3
CH2
H2C
CH3
(5)
(30) (?)
Chromatography Gets Busy
C1-DBT
C2-DBT
C3-DBT
C4-DBT
Additional PAHs
– Biogenic (transformation of natural
precursors)
• Yulin et al. (1996) Biogenic Polycyclic Aromatic
Hydrocarbons in an Alaskan Arctic Lake Sediment,
Polycyclic Aromatic Compounds, 9(1-4).
– Petrogenic (fossil fuels)
– Pyrogenic (burning of organic materials)
Phenanthrene Retene Perylene
Click here for past blog on retene.
Petrogenic vs. Pyrogenic
Advanced – 2D-GC-TOF-MS
• Cost – Highest
• Interpretation – Difficult
• Time – slow
• Can look for anything organic
• Advantage – separation + mass spectra id +
sensitivity
• Can be qualitative or semi-quantitative
Diesel – Gas Station - Canada
Middle East Crude Oil Investigation
Alkyl Phenanthrenes/Anthracenes
Alkyl Naphthalenes
Alkyl Benzenes
Alkanes
Middle East Crude Oil 1
Saskatchewan Crude
Middle East Crude Oil 2
Middle East Crude Oil 3
Middle East Crude Oil Investigation
www.chemistry-matters.com 41
Stable Isotopes – CSIA
“DNA” Fingerprinting
-40
-35
-30
-25
-20
-15
δ13
C(‰)
Compound
• Stable isotope data gives a “signature” to samples
• Samples may be linked or differentiated
O
Case Study
Residents have
allegedly been
exposed to PAHs
released from a local
industry. Exposure
pathways include
inhalation of ambient
air and incidental
ingestion of soil
Investigation
A number of techniques were
completed including:
– Chemical fingerprinting
– Molecular diagnostic ratios
– Statistical Analysis
• Cosine Theta Analysis
Sampling
www.chemistry-matters.com 45
Suspected Source
Unknown
Human Habitation/
Background
Chemical Fingerprint
Molecular Diagnostic Ratios
0
2
4
6
8
10
12
14
16
18
20
0.0 0.5 1.0 1.5 2.0 2.5
FLRN/PYR
PHEN/ANTH
Unknown Human Habitation Suspected Source
Petrogenic
Sources
After Sicre et al 1987, Budzinski et al 1997, Tam et al 2001 and Neff et al 2005
Mixed Sources
Pyrolytic SourcesMixed Sources
Cosine Theta Analysis
An analysis of the matrix of similarity
coefficients between several different
samplesOrthogonal
Dissimilar
Co-linear, similar compositions
Theoretical Vector
1.00, 0o
Theoretical Vector
0.00, 90o
Human Habitation/Background
0.995
Suspected Source
0.586
Unknown
Results of Study
–Independent lines of evidence were
developed to indicate the potential
source of PAHs in soils
–Multiple forensic techniques supported
these lines of evidence
–Conclusion: PAHs found at residence
shared similar properties to those of
human habitation or background
– Not similar to the suspected source
Environmental Forensics in the Gulf
Oil Spill
• Reddy et al. sampled oil directly above well to conduct
comprehensive characterization
– Gas isotopes, GOR, fluid characteristics, API etc.
– Fingerprinted with 2D-GC-TOF
– Could distinguish between crudes
Reddy et al. 2011, PNAS Early Edition, p.1-6
Environmental Forensics in the Gulf
Oil Spill
• Hall et al. took 41 samples (slicks, scrapings off rocks,
grasses and debris, sand patties etc)
• Oxidized hydrocarbons comprised of more than 50% of
extractable hydrocarbons
• Used 2D-GC-TOF of samples compared to oil to assess
weathering of oil spill using chemometric techniques
Hall et al. 2013, Marine
Pollution Bulletin, in
press
Environmental Forensics in the Oil
Sands
Environmental Forensics in the Oil
Sands
Alberta Oil Sands
• Discovered by aboriginals and used to
waterproof canoes – “tar sands”
– “Tar sands” is a dirty term
• In 1719, European fur traders received
sample at Hudson’s Bay Company
• In 1783, first European saw them
personally
• Development began in 1967 by (now
known as) Suncor
Environmental Forensics in the Oil
Sands
• 2009 Kelly et al. (Schindler)
examined water and snow
PAHs near oil sands
development
• Upstream [PAC] <
downstream [PAC] (p<0.05)
• Study was generally ignored
by industry but is cited as the
first attempt to assess
environmental impacts from
oil sands development
Kelly et al. 2009, PNAS, 106, 52, p.22346
Environmental Forensics in the Oil
Sands
• Kurek et al. sampled local
lake sediments (no flow)
• Sediment dating (Pb/Cs)
combined with PAH analysis
• PAHs sharply increased in
lake sediments in ~1970 (but
are still well below guidelines)
• Important study:
– Demonstrated that inputs were
occurring
– Established historical baseline
(hadn’t been done previously)
• No longer a question of if, now
it is question of how much
Kurek et al. 2013, PNAS, 110, 5, p.1761
Environmental Forensics in the Oil
Sands
• Jautzy et al. sampled
local lake sediments (no
flow)
• Sediment dating (Pb/Cs)
combined with PAH
analysis & compound
specific isotopic analysis
• Additional line of
evidence showing isotope
shift in DBT
• Increase due to
deposition of bitumen in
dust particles with erosion
of open pit mines
Jautzy et al. 2013, ES&T, 47, p.6155
Environmental Forensics in the Oil
Sands
• Lundin et al. sampled scat
from wolf, moose and caribou
around SAGD facilities
• DNA testing, hormone testing,
scat detection dogs, etc.
• Higher concentrations of
PAHs (NAP and alkyl-NAP) in
moose scat near SAGD
compared to control locations
• Suggests that SAGD facilities
may still be implicated
Lundin et al. 2013, ISPAC 2013, Tues,11:00 AM
Environmental Forensics Resources
Societies and Organizations
• International Network of Environmental Forensics
(INEF)
• Association for Environmental Health & Sciences
(AEHS) Foundation
• International Society of Environmental
Forensics (ISEF)
University Degrees and Training
• Masters degree – University of Strathclyde
• Bachelor Degree – Bangor University
• University of Florida – Certificate program
• Many courses on Environmental Forensics
offered at Universities
• Environmental Forensics certification
(AEHS Foundation and others)
Questions?
Contact Info:
Chemistry Matters
Court Sandau
Email: csandau@chemistry-matters.com
Twitter: @Chem_Matters
Slideshare: www.slideshare.net/csandau
Please visit our website for related information, case
studies and blogs. www.chemistry-matters.com
Got a question, post it to our website, HERE.

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ISPAC2013 plenary talk - Environmental Forensics and PAHs

  • 1. Use of PAHs in Environmental Forensics Presented by: Court Sandau, PhD, PChem ISPAC 2013 Corvallis, OR
  • 2. Environmental Forensics • What is it? • Analytical issues with PAHs and EFI • Expanding PAHs (beyond 16) • PAHs and EFIs – examples and case studies 2 For case study on PAHs and a pipeline oil spill, see a part blog on our website: http://chemistry-matters.com/pipeline-spill/ For more information on PAHs, click here to see our website page on PAHs.
  • 3. Environmental Forensic Investigation The systematic examination of historical and environmental information (which may be used in litigation) to allocate responsibility for contamination “The application of scientific methods used to identify the origin and timing of a contaminant release” See our website for more information on environmental forensic investigations.
  • 4. Disciplines in Environmental Forensics • Chemistry • Statistics • Engineering • Microbiology • Hydrogeology • Soil Science • Toxicology • Biology • Ecology • Litigation Experience • And others….
  • 5. Birthplace of Environmental Forensics Exxon Valdez 1989 Term “Environmental Forensics” coined in Dr. Robert Morrison’s first books since it was used in a peer reviewed publication. 5
  • 8. EFI Video Click here for link to video on slideshare.
  • 9. Two Categories of EFIs Academic & Research Liability Driven
  • 10. Litigation and Liability Driven EFIs • Adversarial process • Goal – make you look bad or incompetent while making themselves look good/sympathetic • They are trying to tell if you are telling the truth or not • Good science does not necessarily prevail • Unfortunately, science is complicated (scientific literacy 28% in 2007) • Need to prove it beyond a reasonable doubt 10
  • 11. Differences Between Legal and Research • Documentation, Documentation, Documentation Project id. Address Project id.DateDate Date Notes and pictures/videos
  • 12. Differences Between Legal and Research • Documentation • Sample Handling • Chain of Custody
  • 13. Differences Between Legal and Research • Documentation • Sample Handling • Chain of Custody • Laboratory Competence • Standard Procedures • Communicating Results
  • 14. Carpet Dust Sampling • Must follow standardized procedures where available • Difficult to change approaches • Validation required if methodology changes Designation: D 5438 – 05 Standard Practice for Collection of Floor Dust for Chemical Analysis1 This standard is issued under the fixed designation D 5438; the number immediately following the desig original adoption or, in the case of revision, the year of last revision. A number in parentheses indicates th superscript epsilon (e) indicates an editorial change since the last revision or reapproval. 1. Scope 1.1 This practice covers a procedure for the collection of a sample of dust from carpets and bare floors that can be analyzed for lead, pesticides, or other chemical compounds and elements. 1.2 This practice is applicable to a variety of carpeted and bare floor surfaces. It has been tested for level loop and plush pile carpets and bare wood floors, specifically. 1.3 This practice is not intended for the collection and evaluation of dust for the presence of asbestos fibers. 1.4 The values stated in SI units are to be regarded as the standard. 1.5 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appro- priate safety and health practices and determine the applica- bility of regulatory limitations prior to use. 2. Referenced Documents 2.1 ASTM Standards: 2 D 422 Test Method for Particle-Size Analysis of Soils D 1356 Terminology Relating to Sampling and Analysis of Atmospheres E 1 Specification for ASTM Thermometers E 337 Test Method for Measuring Humidity with a Psy- larger, embedded in carpet household vacuum cleaners 3.1.2 surface dust—soil proximately 5-µm equivalen adhering to floor surfaces a hold vacuum cleaners. 4. Summary of Practice 4.1 The sampling metho from work published in Rob (4). 4.2 Particulate matter is floor by means of vacuu through a sampling nozzle and the particles are separat cyclone is designed to effic approximately 5-µm mean However, much smaller par efficiencies. The sampling and suction adjustments to air velocity for the removal and bare floor surfaces, so be repeated. NOTE 1—Side-by-side compa upright vacuum cleaner revealed Designation: D 422 – 63 (Reapproved 2002)e 1 Standard Test Method for Particle-Size Analysis of Soils1 This standard is issued under the fixed designation D 422; the number immediately following the designation indicates the year of original adoption or, in the case of revision, the year of last revision. A number in parentheses indicates the year of last reapproval. A superscript epsilon (e) indicates an editorial change since the last revision or reapproval. HVS-3 Vacuum Cleaner
  • 15. Commercial Laboratory PAH Analysis • Methods vary from lab to lab • Quantification – Semi-quantitative methods with surrogates – Quantitative methods with labeled internal standards • Analytes measured – Routine EPA – Routine EPA+ – Deluxe EPA compounds with substituted PAHs and then some (up to 63 compounds in an analysis)
  • 16. www.chemistry-matters.com 16 US EPA Priority Pollutants PAH Compounds benzo[k]fluoranthene benzo[a]pyrene benzo[b]fluoranthenepyrenefluoranthenechrysene fluorenephenanthreneacenaphthyleneanthraceneacenaphthenenaphthalene benzo[ghi]perylenedibenz[a,h]anthracene indeno[1,2,3-cd]pyrene benzo[a]anthracene 2-ring 3-ring 4-ring 5-ring 6-ring LMW HMW
  • 17. Analysis of PAHs S Retention Time RelativeResponse
  • 18. Interlaboratory Comparisons Method 8270C • Interlaboratory study conducted • Each lab measured homogeneous soil sample 4 times over a ~ week • Requested standard PAH method • Compared variability amoung labs and within each laboratory
  • 21. Pyrene 0.00 0.10 0.20 0.30 0.40 0.50 0.60 0.70 0.80 0.90 All Labs Lab A Lab B Lab C Lab D Lab E Lab F Lab G Lab H mg/kg Mean Value Maximum Value Minimum Value FAL - Coarse (0.40)
  • 22. Results • Laboratory variability issues amoung laboratories • Sample to sample variability within the laboratories Variability can be measured and controlled with a good data validation program
  • 23. Method Comparison - PAHs Low Resolution MS Method • EPA Method 8270C • Full Scan analysis • No confirmation ions or ratios • Inappropriate surrogate standards • Many versions of method High Resolution MS Method • Modified California Method (Carb 429) • IDMS quantitation • Less likely to have interferences present • Isotopically labeled standards • More accurate and precise • Better data = better decisions
  • 24. PAH Analysis • Many interferences exist in low molecular weight range – Depends on matrix, clean up method • Specificity of HRMS allows better accuracy and precision • Comes at a cost – 4-6x Difference in measuring 252 versus 252.30928 Benzo(a)pyrene
  • 25. Internal Standards vs. Surrogates naphthalene phenanthrene benzo(a)pyrene N+ O O- F * * * * * *13 C * * * * ** * * * *
  • 26. Isotope Dilution Quantification • Standards behave exactly like compounds being analyzed • Loss of analytes during method, included in measurement • Matrix interferences in method, can usually be seen with standards as well • THE most accurate measurement available
  • 27. Is more expensive better? Experiment: • SRM – determine accuracy • Duplicate – determine precision • Unknown duplicates to compare results Compared methods, not laboratories Lab A – ID-HRMS Lab B- LRMS, surrogates
  • 29. PAH Duplicate Results 0 20 40 60 80 100 120 BaA BaP BbF BkF CHRY FLUOR PHEN PYR Sample 1 Sample 2 0 20 40 60 80 100 120 BaA BaP BbF BkF CHRY FLUOR PHEN PYR Sample 1 Sample 2 Compounds Compounds Concentration (ng/g) Concentration (ng/g) Lab B Lab A 100% 92% 111% 100% 86% 94% 101% 90% RPD 3% 8% 15% 16% 18% 17% 27% 11% RPD
  • 31. Causes of Overestimation • Incomplete cleanup, residue matrix in extracts • Co-elution of other PAHs not being monitored
  • 32. Data Quality for PAHs • Low resolution surrogate MS methods for PAHs can be highly variable between laboratories • Sites driven by PAH risk require IDMS – Sensitivity – for the guidelines – Specificity – for the interferences that are naturally present in samples • IDMS methods are suggested for forensics investigations – May reduce variability of diagnostic ratios
  • 33. Diagnostic Ratios Ratios Values / Sources References Phenanthrene / Anthracene < 5 = Pyrogenic; > 5 = Petrogenic Neff et al., 2005 Fluorene / Pyrene + 1 = Pyrogenic. < 1 = Petrogenic Neff et al., 2005 Indeno(1,2,3-cd)pyrene / (Indeno(1,2,3-cd)pyrene + Benzo(g,h,i)perylene > 0.1 = Combustion Motelay-Massei et al 2007; Yunker et al., 2002 Fluoranthrene/ Pyrene < 1 = Petrogenic; >1 Pyrogenic Motelay-Massei et al 2007 LMW / HMW < 1 = Combustion Zhang et al 2005; Benzo(a)pyrene / Benzo(a)pyrene + Chrysene < 0.2 = Petrogenic; > 0.35 = Combustion Zhang et al 2005; Zhang et al 2007 • Decrease analytical variability with better methods • Some good, some not as good – use what fits? • Good for bulk characterization – what about further distinction of sources
  • 34. Expanding the List of PAHs Alkylated-PAHs and Other PAHs C1-Phenanthrenes 1 2 3456 7 8 9 10 CH3 C2-Phenanthrenes Phenanthrene CH3 CH3 CH3 H3C CH2 CH3 C3-Phenanthrenes C4-Phenanthrenes… (?) CH3 CH3 CH3 CH2 H2C CH3 (5) (30) (?)
  • 36. Additional PAHs – Biogenic (transformation of natural precursors) • Yulin et al. (1996) Biogenic Polycyclic Aromatic Hydrocarbons in an Alaskan Arctic Lake Sediment, Polycyclic Aromatic Compounds, 9(1-4). – Petrogenic (fossil fuels) – Pyrogenic (burning of organic materials) Phenanthrene Retene Perylene Click here for past blog on retene.
  • 38. Advanced – 2D-GC-TOF-MS • Cost – Highest • Interpretation – Difficult • Time – slow • Can look for anything organic • Advantage – separation + mass spectra id + sensitivity • Can be qualitative or semi-quantitative Diesel – Gas Station - Canada
  • 39. Middle East Crude Oil Investigation Alkyl Phenanthrenes/Anthracenes Alkyl Naphthalenes Alkyl Benzenes Alkanes
  • 40. Middle East Crude Oil 1 Saskatchewan Crude Middle East Crude Oil 2 Middle East Crude Oil 3 Middle East Crude Oil Investigation
  • 41. www.chemistry-matters.com 41 Stable Isotopes – CSIA “DNA” Fingerprinting -40 -35 -30 -25 -20 -15 δ13 C(‰) Compound • Stable isotope data gives a “signature” to samples • Samples may be linked or differentiated O
  • 42. Case Study Residents have allegedly been exposed to PAHs released from a local industry. Exposure pathways include inhalation of ambient air and incidental ingestion of soil
  • 43. Investigation A number of techniques were completed including: – Chemical fingerprinting – Molecular diagnostic ratios – Statistical Analysis • Cosine Theta Analysis
  • 45. www.chemistry-matters.com 45 Suspected Source Unknown Human Habitation/ Background Chemical Fingerprint
  • 46. Molecular Diagnostic Ratios 0 2 4 6 8 10 12 14 16 18 20 0.0 0.5 1.0 1.5 2.0 2.5 FLRN/PYR PHEN/ANTH Unknown Human Habitation Suspected Source Petrogenic Sources After Sicre et al 1987, Budzinski et al 1997, Tam et al 2001 and Neff et al 2005 Mixed Sources Pyrolytic SourcesMixed Sources
  • 47. Cosine Theta Analysis An analysis of the matrix of similarity coefficients between several different samplesOrthogonal Dissimilar Co-linear, similar compositions Theoretical Vector 1.00, 0o Theoretical Vector 0.00, 90o Human Habitation/Background 0.995 Suspected Source 0.586 Unknown
  • 48. Results of Study –Independent lines of evidence were developed to indicate the potential source of PAHs in soils –Multiple forensic techniques supported these lines of evidence –Conclusion: PAHs found at residence shared similar properties to those of human habitation or background – Not similar to the suspected source
  • 49. Environmental Forensics in the Gulf Oil Spill • Reddy et al. sampled oil directly above well to conduct comprehensive characterization – Gas isotopes, GOR, fluid characteristics, API etc. – Fingerprinted with 2D-GC-TOF – Could distinguish between crudes Reddy et al. 2011, PNAS Early Edition, p.1-6
  • 50. Environmental Forensics in the Gulf Oil Spill • Hall et al. took 41 samples (slicks, scrapings off rocks, grasses and debris, sand patties etc) • Oxidized hydrocarbons comprised of more than 50% of extractable hydrocarbons • Used 2D-GC-TOF of samples compared to oil to assess weathering of oil spill using chemometric techniques Hall et al. 2013, Marine Pollution Bulletin, in press
  • 51. Environmental Forensics in the Oil Sands
  • 52. Environmental Forensics in the Oil Sands
  • 53. Alberta Oil Sands • Discovered by aboriginals and used to waterproof canoes – “tar sands” – “Tar sands” is a dirty term • In 1719, European fur traders received sample at Hudson’s Bay Company • In 1783, first European saw them personally • Development began in 1967 by (now known as) Suncor
  • 54. Environmental Forensics in the Oil Sands • 2009 Kelly et al. (Schindler) examined water and snow PAHs near oil sands development • Upstream [PAC] < downstream [PAC] (p<0.05) • Study was generally ignored by industry but is cited as the first attempt to assess environmental impacts from oil sands development Kelly et al. 2009, PNAS, 106, 52, p.22346
  • 55. Environmental Forensics in the Oil Sands • Kurek et al. sampled local lake sediments (no flow) • Sediment dating (Pb/Cs) combined with PAH analysis • PAHs sharply increased in lake sediments in ~1970 (but are still well below guidelines) • Important study: – Demonstrated that inputs were occurring – Established historical baseline (hadn’t been done previously) • No longer a question of if, now it is question of how much Kurek et al. 2013, PNAS, 110, 5, p.1761
  • 56. Environmental Forensics in the Oil Sands • Jautzy et al. sampled local lake sediments (no flow) • Sediment dating (Pb/Cs) combined with PAH analysis & compound specific isotopic analysis • Additional line of evidence showing isotope shift in DBT • Increase due to deposition of bitumen in dust particles with erosion of open pit mines Jautzy et al. 2013, ES&T, 47, p.6155
  • 57. Environmental Forensics in the Oil Sands • Lundin et al. sampled scat from wolf, moose and caribou around SAGD facilities • DNA testing, hormone testing, scat detection dogs, etc. • Higher concentrations of PAHs (NAP and alkyl-NAP) in moose scat near SAGD compared to control locations • Suggests that SAGD facilities may still be implicated Lundin et al. 2013, ISPAC 2013, Tues,11:00 AM
  • 59. Societies and Organizations • International Network of Environmental Forensics (INEF) • Association for Environmental Health & Sciences (AEHS) Foundation • International Society of Environmental Forensics (ISEF)
  • 60. University Degrees and Training • Masters degree – University of Strathclyde • Bachelor Degree – Bangor University • University of Florida – Certificate program • Many courses on Environmental Forensics offered at Universities • Environmental Forensics certification (AEHS Foundation and others)
  • 61. Questions? Contact Info: Chemistry Matters Court Sandau Email: csandau@chemistry-matters.com Twitter: @Chem_Matters Slideshare: www.slideshare.net/csandau Please visit our website for related information, case studies and blogs. www.chemistry-matters.com Got a question, post it to our website, HERE.