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^Precise Research. Proven Results.
A nalytical Report
Fluorochemical Characterization of Aqueous Samples Decatur Outfall 001 FC Monitoring (E06-0094)
Exygen Research Laboratory Report No. L0007528 Testing Laboratory Exygen Research 3058 Research Drive
State College, PA 16801
Requester Gary A. Hohenstein Environmental Manager, Special Projects, EHS Operations 3M Bldg, 42-2E-27 St. Paul, MN 55133
exygen.com
1 Introduction
Results are reported for the analysis of aqueous samples received by Exygen Research (Exygen) from PACE Analytical. The Exygen study number assigned to the project is L0007528.
Specific fluorochemical characterization by liquid chromatography / tandem mass spectrometry (LC/MS/MS) was requested for all samples. A total of 8 samples (including field duplicates, blanks, and spikes) were received for analysis.
The samples were prepared and analyzed by LC/MS/MS for the following list of fluorochemicals:
Table 1: Target Analysis
Compound Name Perfluorobutanesulfonate (PFBS) Perfluorohexanesulfonate (PFHS) Perfluoroodanesulfonate (PFOS) Perfluorobutvric Acid Perfluorooentanoic Acid Perfluorohexanoic Acid PerfluoroheDtanoic Acid Perfluorooctanoic Acid Perfluorononanoic Acid Perfluorodecanoic Acid Perfluoroundecanoic Acid Perfluorododecanoic Acid Perfluorobutanesulfonamide (PFB Amide) Perfluorooctanesulfonamide 2-(N-methvloerluorobutanesulfonamido)ethvl alcohol
Acronvm 04 Sulfonate C6 Sulfonate C8 Sulfonate C4 Acid C5 Acid C6 Acid C7 Acid C8 Acid C9 Acid C10 Acid C11 Acid C12 Acid FBSA FOSA Me-FBSE-OH
The analytical methods used were originally developed for groundwater samples and were validated by Exygen. The validation protocol and results are on file with Exygen. Only the C8 Sulfonate, FOSA, and C8 Acid were included in the original method validation. It should be noted that the quality control elements included in this analysis demonstrate the applicability of the method to the additional analytes.
2 Sample Receipt
The water samples were submitted in plastic containers. Samples were received at ambient temperature. Samples were stored at 4C from receipt until analysis. Eight individual containers were received. Field samples were collected on 2/14/06 and 2/15/06. Samples were received on 2/16/06. Chain-of-custody information is presented in Attachment C.
PAGE 2 OF5
3 Holding Times
Field and laboratory spikes of these fluorochemicais have shown stability for periods greater than 90 days. Samples were analyzed within 60 days of collection.
4 Methods - Analytical and Preparatory
4.1 LC/MS/MS
4.1.1 Sample Preparation for LC/MS/MS Analysis
Water samples were initially treated with 200 uL of 250 mg/L sodium thiosulfate solution to remove residual chlorine. Solid phase extraction (SPE) was used to prepare the samples for LC/MS/MS analysis. A 40 mL portion of sample was transferred to a C i8 SPE cartridge. The cartridge was eluted with 5 mL of 100% methanol. This treatment resulted in an eight-fold concentration of the diluted samples prior to analysis.
4.1.2 Sample Analysis by LC/MS/MS
In HPLC, an aliquot of extract is injected and passed through a liquid-phase chromatographic column. Based on the affinity of-the analyte for the stationary phase in the column relative to the liquid mobile phase, the analyte is retained for a characteristic amount of time. Following HPLC separation, ES/MS provides a rapid and accurate means for analyzing a wide range of organic compounds, including fluorochemicais. Electrospray is generally operated at relatively mild temperatures; molecules are ionized, fragmented, and detected. Ions characteristic of known fluorochemicais are observed and quantitated against standards.
A Hewlett-Packard HP1100 HPLC system coupled to a PE Sciex API 4000 MS/MS was used to analyze the sample extracts. Analysis was performed using selected reaction monitoring (SRM). Samples were extracted on 2/20/06. Samples were analyzed on 3/17/06 and 3/18/06. Raw analytical data is provided in Attachment D.
5 Analysis
5.1 Calibration
A 9-level calibration curve was analyzed at the beginning and throughout the analytical sequence for the compounds of interest. The calibration points, were prepared at 0, 25, 50, 100, 250, 500, 1000, 2500, and 5000 ng/L (ppt) for LC/MS/MS analysis. The instrument response versus the concentration was plotted for each point. Using linear regression with 1/x weighting, the slope, y-intercept and correlation coefficient (r) and coefficient of determination (r2) were determined. A calibration curve is acceptable if r >0.985 (r2> 0.970).
Calibration standards are prepared using the seme SPE procedure used for samples.
All calibration criteria were met for this analysis.
5.2 Blanks
Extraction blanks were prepared and analyzed with every extraction batch of samples. The extraction blanks should riot have any target analytes present at or above the concentration of the low-level calibration standard. For these samples, the extraction blanks were compliant.
PAGE 3 OF 5
Instalment blanks in the form of clean methanol solvent were also analyzed after every highlevel calibration standard, and after known high-level samples. Again, the blanks should not have any target analytes present at or above the low-levei calibration standard. For the samples presented here the instrument blanks are compliant.
5.3 Surrogates
Surrogate spikes are not a component of the LC/MS/MS analytical methods.
5.4 Matrix Spikes
Field and laboratory spikes were prepared using all compounds of interest. Field spikes were prepared by adding a measured volume of field sample to a container spiked with the target analytes by the laboratory prior to shipping containers for sample collection. Laboratory spikes consisted of aliquots of un-spiked field samples that were fortified at the laboratory at the time of extraction. Field blank spikes consisted of laboratory water fortified at the laboratory and shipped with the sample containers to the field and back to the laboratory for analysis. Laboratory control spikes (see section 5.6) are samples of laboratory water spiked at the time of extraction. Each type of spike provides information needed to assess analyte stability, extraction efficiency, and matrix effects that may impact analytical results. Matrix spike recoveries are given in Attachment B. Please see Section 5.7 for additional discussion of matrix spike recoveries.
5.5 Duplicates
Field and laboratory duplicates were prepared for each field sample. Duplicate results are given along with the sample results in Attachment A.
5.6 Laboratory Control Samples
For LC/MS/MS analyses, Milliq water was spiked with all compounds of interest at 100 and 500 ng/mL during each extraction set. All recoveries for all compounds were between 70 130% in each LCS. Results are given along with the raw data in Attachment D.
5.7 Statement of Accuracy
Based on results of field blank spikes and laboratory control spikes, the analytical method accuracy for all analytes is 30%. Based on the results of field and laboratory matrix spike samples, the overall accuracy for the analysis is as follows:
C12 Acid and Me-FBSE-OH 40%
C4 Sulfonate 50%
C4 Acid and C5 Acid are considered as screening quality because of high and variable spike recoveries
All others 30%
All spike recovery data are reported in the data fables.
PAGE4 OF5
5.8 Data Summary
Please see Attachment A for a detailed listing of the analytical results. Results are reported in parts per billion (ppb) (ng/ml_). Please note that the limit of quantitation is 1.0 ng/mL for all compounds except MeFBSE-OH and C4 Acid, which have a quantitation limit of 4.0 ng/mL.
6 Data/Sample Retention
Samples are disposed of one month after the report is issued unless otherwise specified. All electronic data is archived on retrievable media and hard copy reports are stored in data folders maintained by Exygen.
7 Attachments
7.1 AttachmentA Results 7.2 Attachment B: Matrix Spike Recoveries 8.3 Attachment C: Chain of Custody 8.4 Attachment D: Raw Analytical Data
9 Signatures
Other Lab Members Contributing to Data C hrissy Edwards
PAGE 5 OF5
Section A
Report^
Summary of Fluorochemical Residues in Outfall 001 Effluent for E06-0094
Sample ID
Outfall 001 Effluent Outfall 001 Effluent* Outfall 001 Effluent Dup
Travel Blank Equipment Blank
, \
\ \ \
C4 A cid" Perfluorobutyric Acid
17.6 22.1 19.7 ND ND
Analyte Found (ng/mL)
C5 Acid
C6 Acid
Perfluoropentanoic Acid Perfluorohexanolc Acid
1.91 2.00 1.62 ND ND
2.40 2.30 2.33 ND ND
C7 Acid Perfluoroheptanoic Acid
1.22 1.19 1.17 ND ND
Sam ple ID Outfall 001 Effluent Outfall 001 Effluent* Outfall 001 Effluent Dup
Travel Blank Equipment Blank
Sample ID Outfall 001 Effluent Outfall 001 Effluent* Outfall 001 Effluent Dup
Travel Blank Equipment Blank
C8 Acid Perfluorooctanolc Acid
. 2.12 2.11 2,12 ND ND
Analyte Found (ng/mL)
C9 Acid
C10 Acid
Perfluorononanoic Acid Perfluorodecanoic Acid
ND ND
ND ND
ND ND
ND ND
ND ND
C11 Acid Perfluoroundecanoic Acid
ND ND ND ND ND
C12 Acid Perfluorododecanoic Acid
ND . ND ND ND ND
Analyte Found (ng/mL)
C4 Sulfonate
C6 Sulfonate
Perfluorobutanesulfonate Perfluorohexanesulfonate
87.0 95.2
ND ND
79.9 ND \ ND
ND ND ND
0 8 Sulfonate Perfluorooctanesulfonate
8.17 8.06 8.61 ND ND
Analyte Found (ng/mL)
Sample ID
Outfall 001 Effluent Outfall 001 Effluent* Outfall 001 Effluent Dup
Travel Blank Equipment Blank
FBSA
10.4 11.3 10.2 ND ND
FOSA
ND ND ND ND . ND ,
Me-FBSE-OH**
15.0 14.1 12.2 ND ND
ND = Not detected = Response between 0 and 1 ng/mL. **ND = Not detected = Response between 0 and 4 ng/mL.
' Laboratory Duplicate
0006
J ^ 3 03055i8 Research Drive -# ^ k S Statate College, PA 16801, USA
VT: 800.281.3219 F: 814.272.1019 exygen.com
Section B
CH
Recovery Summary of Fluorochemical Residues in Outfall 001 Effluent for E06-0094
Sample Description
Outfall 001 Effluent
Low Field Spike
C4 Acid*
C5 Acid
C6 Acid
C7 Acid
Amount Amt Found Amount
Amt Found Amount
Amt Found Amount
Amt Found Amount
Spiked in Sample Recovered Recovery in Sample Recovered Recovery in Sample Recovered Recovery in Sample Recovered Recovery
(ng/mL) (ng/mL) (ng/mL) (%)
(ng/mL) (ng/mL) (%)
(ng/mL) (ng/mL) (%>
(ng/mL) (ng/mL) (%)
10
17.6,
49.9 323
1.91
28.1 262
2.40
13.0 106
1.22
10.8 96
Outfall 001 Effluent
High Field Spike
100
17.6 . 214
196
1.91
197 195 2.40 75.0 73
1.22 83.8 83
Outfall 001 Effluent Spk C Low Lab Spike
1
17.6 21.4 **
1.91
7.73 582
2.40
3.41 101
1.22
2.16 94
Outfall 001 Effluent Spk O High Lab Spike
100
17.6
485 \
467
1.91
494 494
2.40
135 133 1.22
129 128
Field Blank
Low Field Spike
10
ND
10.2 , 102
ND
10.3 103
ND
10.3 103
ND
12.0 120
Field Blank
High Field Spike
100 ND
101 101
ND
119 119
ND
99.9 100
ND
114 114
Sample Description Outfall 001 Effluent
Low Field Spike
Outfall 001 Effluent
High Field Spike
Outfall 001 Effluent Spk C Low Lab Spike
O utfall 001 Effluent Spk O High Lab Spike
Field Blank
Low Field Spike
Field Blank
High Field Spike
Ct Acid
C9 Acid
C10 Acid
C11 Acid
Amount Amt Found Amount
Amt Found Amount
Amt Found Amount
Amt Found Amount
Spiked in Sample Recovered Recovery ih Sample Recovered Recovery in Sample Recovered Recovery in Sample Recovered Recovery
(ng/mL) (ng/mL) (ng/mL) (V.)
(ng/mL) (ng/mL) (%)
(ng/mL) (ng/mL) <%)
(ng/mL) (ng/mL) (%)
10 2.12 12.1 100 ND
10.9 109
ND
10.3 103
ND
9.63 96
100 2.12 81.2 79
ND \
92.4
92
ND
94.0 94
ND 83.6 84
1 2.12 2.87 75 100 2.12 95.2 93
ND ,1.09 109 ND 119 119
ND ND
1.02 102
ND
0.943
94
114 114
ND
121 121
10 ND
10.8 108
ND
10.6 \ 106 ND 9.17 92
ND
11.2 112
100 ND
100 100
ND
105 105
ND
97.6 98
ND
111 111
ND = Not detected = Response between 0 and 1 ng/mL.
*ND = Not detected = Response between 0 and 4 ng/mL.
.
"Sample residue exceeded the spiking level by more than 4 times; therefore an accurate recovery cannot be calculated.
0007
J&303055S8 Research Drive iT m S tSatatte College, PA 16801, USA
YJ: 800.281.3219 F: 814.272.1019 exygen.com
CH
Recovery Summary of Fluorochemical Residues in Outfall 001 Effluent for E06-0094 Continued
Sample Description Outfall 001 Effluent
Low Field Spike
Outfall 001 Effluent
High Field Spike
Amount Spiked (ng/mL)
C12 Acid
C4 Sulfonate
C6 Sulfonate
C8 Sulfonate
Amt Found Amount
Amt Found Amount
Amt Found Amount
Amt Found Amount
in Sample Recovered Recovery in Sample Recovered Recovery in Sample Recovered Recovery in Sample Recovered Recovery
(ng/mL) (ng/mL) (%)
(ng/mL) (ng/mL) (%)
(ng/mL) (ng/mL)____ (%)
(ng/mL) (ng/mL) (%)
10
ND ,
6.00
60
87.0
113
**
ND
12.6 126
8.17
19.6 114
100 ND , 65.8 66 87.0 266 179 ND 98.2 98 8.17 112 104
Outfall 001 Effluent Spk C Low Lab Spike
1
ND
0:863
86
87.0
92.8
**
ND 1.58 158 8.17 9.47 **
Outfall 001 Effluent Spk D High Lab Spike
100
ND
103 \
103
87.0
231 144
ND
92.9 93
8.17
111 103
Field Blank
Low Field Spike
10
ND
10.1 \ 101
ND
9.59 96
ND
12.0 120
ND
9.75 98
Field Blank
High Field Spike
100 ND 101 11 ND 98.5 99 ND 111 i n
ND 111 111
Sample Description Outfall 001 Effluent
Low Fiald Splka
Outfall 001 Effluent
High Field Spike
Outfall 001 Effluent Spk C Low Lab Spike
Outfall 001 Effluent Spk O High Lab Spike
Field Blank
Low Field Spike
Field Blank
High Field Spike
FBSA
FOSA
Me-FBSE-OH*
Amount Amt Found Amount
Amt Found Amount
Amt Found Amount
Spiked in Sample Recovered Recovery in.Sample Recovered Recovery in Sample Recovered Recovery
(ng/mL) (ng/mL) (ng/mL)____ <%)
(ng/mL) (ng/mL) (%)
(ng/mL) (ng/mL)____ (%)
10 10.4 20.3 99
N.
11.3 113
15.0
21.4 64
100 10.4
102 92
ND . 94.1
94
15.0
77.4 62
1 10.4 12.1 **
ND
,1.69
169
15.0
17.0
**
100 10.4
105 95
ND
93.8,
94
15.0
132 117
10
ND
10.4 104
ND
9.08 \ 91
ND 10.3 103
100 ND
106 106 ND 86.1 86
ND 81.5 82
ND = Not detected = Response between 0 and 1 ng/mL.
.
*ND = Not detected = Response between 0 and 4 ng/mL.
"Sample residue exceeded the spiking level by more than 4 times; therefore an accurate recovery cannot be calculated.
0008
J^30,35058 Research Drive
v rm s tSatatte College, PA 16801, USA
YJ: 800.281.3219 F: 814.272.1019 exygen.com
Section C
3058 Research Drive State College, PA 16801
Phone: 814-272-1039 Fax: 814-231-1580
Lopin
Login Group: L0007528
Login #: Project:
Company Name: Submitted By: Login Type: Started: Date Start: Due Date: Login Initiated*:
7639 P0000522
3M Kent Lindstrom Immediate Receipt of Samples True 02/16/2006 02/26/2006 02/16/2006
Conform COC Sample: Conform COC:
Conform Sample: Conform Request:
True True
True True
* Dates entered into "Login Initiated" field prior to 1/5/06 reflect dates of receipt. The field was formerly called "Received Date"
Received By:
Ammerman, Mark
Spread Sample:
Label:
Exygen SD/PI: Risha, Karen
Project Title/Type: Groundwater Sampling, Decatur AL / ROUTINE
Login Notes:
Packaae PK0008674
Carton
Packages / Containers
Date / Condition
ShiDDer/ ID
Received Date: 2/16/06 10:28 Package & Contents Uncompromised
FEDEX 8540 9649 0291
Temo. Control/TemD.
None 20.0
Direction / Handled Bv
RECEIVED Ammerman, Mark
Container # C0151093 C0151094 C0151095 C0151096 C0151097 C0151098 C0151099 C0151100
Gross Weiaht dH
Container TvDe
602.00 g
500 ml Clear Plastic Narrow
601.50 g
500 ml Clear Plastic Narrow
611.50 g
500 ml Clear Plastic Narrow
250.00 g
500 ml Clear Plastic Narrow
250.50 g
500 ml Clear Plastic Narrow
258.80 g
500 ml Clear Plastic Narrow
260.10 g
500 ml Clear Plastic Narrow
256.70 g
500 ml Clear Plastic Narrow
Preservative NONE NONE NONE NONE NONE NONE NONE NONE
Mfa. Lot
Mfa. ID
2/16/2006 Login.rpt
Report Version: Feb 13 2006 2:43PM Page 1 of 2
Instance:
R0229193
R0229193
Sample ID L0007528-0001 L0007528-0002 L0007528-0003 L0007528-0004 L0007528-0005 L0007528-0006 L0007528-0007 L0007528-0008
Container C0151093 C0151094 C0151095 C0151096 C0151097 C0151098 C0151099 C0151100
Matrix LIQUID LIQUID LIQUID LIQUID LIQUID LIQUID LIQUID LIQUID
Login
Fraction Water
Samples
Sample Equipment Blank
Water
Outfall 001 Effluent
Water
Outfall 001 Effluent Dup
Water
Outfall 001 Effluent 10 ppb Low Sp.
Water
Outfall 001 Effluent 100 ppb High Sp.
Water
Field Control/ Travel Blank
Water
Field Control/ Travel Blank Low Sp. (10 ppb)
Water
Field Control/ Travel Blank High Sp. (100 ppb)
Date Sampled 02/14/2006 02/15/2006 02/15/2006 02/15/2006 02/15/2006
Date Due 02/26/2006 02/26/2006 02/26/2006 02/26/2006 02/26/2006 02/26/2006 02/26/2006 02/26/2006
Login Reviewed By:
Date/Time:
9 /$ ^
2/16/2006 Login.rpt
0010
Report Version: Feb 13 2006 2:43PM Page 2 of 2
Instance:
R0229193
R0229193
ace Analytical
/S e c tio n A
' Required Client Information:
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t J s*
Email To- < t . K r totf\a.ST*tw \
Ph ni 5 l - m - & 5 X Fax Requested Due Date/TAT:
cow \
CHAIN-OF-CUSTODY / Analytical Request Document
The Chain-of-Custody is a LEGAL DOCUMENT. All relevant fields must be completed accurately.
S e c tio n B
Required Project Information:
Report To:
.,
..
W l * . K e . 'O T u m d S T r D v n Copy To:
S e c tio n C Invoice Information: Attention:
Company Name:
Address:
Purchase Order No.:
Pace Quote Reference:
Project Name:
r
U C d to T ttA , 0 |a5 w
Project
L-L* O O l W e v A O A
Pace Project ManagerPace Profile #:
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REGULATORY AGENCY
GROUND WATER
DRINKING WATER
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SITE LOCATION
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R E L IN Q U IS H E D B Y / A F F IL IA T IO N
A C C E P T E D B Y / A F F IL IA T IO N
n DATE
T IM E
SAMPLE CONDITION
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SEE REVERSE SIDE FOR INSTRUCTIONS
ORIGINAL
S A M P L E R N A M E A N D S IG N A T U R E
PRINT Name of SAMPLER: rr_
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SIGNATURE of SAMPLER: ,V is \ <3 ^
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-------- --
DATE Signed (MM / DD / YY)
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ALLQ020rev.3,31 Mar05
Instructions for completing Chain of Custody (COC)
1. Section A and B: Complete all Client information at top of sheet: company name, address, phone, tax, contact (the person to contact if there are questions, and who will receive the final report.), e-mail address (if available), PO#, Project Name and/or Project Number as you would like to see it appear on the report.
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4. Site Location: A separate COC must be filled out for each day of sample collection. Record the two letter postal code for the US state in which the samples were collected.
5. Regulatory Agency: List the program that is guiding the work to ensure proper regulations are followed.
6. Section D: Complete a Sample Description in the "SAMPLE ID' section as you would like it to appear on the laboratory report. The following
information should also be included: the sample matrix, sample type (G (grab) orC (composite). When collecting a composite, the start time and end
time should be documented in the respective boxes. The collection time for a grab (G) sample should be entered in the boxes marked "Composite
End/Grab'), Sample temp at collection (if required by state), the total number of containers, and preservative used.
'
7. Mark if the sample was filtered in the field by marking Y or N in `Filtered' row by the Analysis requested.
8. Requested Analysis: lis t the required analysis and methods on the lines provided and place a check in the, column for the samples requiring the analysis. Additional comments should be referenced in the bottom left hand comer or include attachments for extended lists of parameters.
9. The sampler should print their name in the space provided and sign their name followed by the date of the sampling event at the bottom of the COC in
the spaces designated fo r`SAMPLER NAME AND SIGNATURE'.
'
',
,.
10. When relinquishing custody of the samples to a representative of the laboratory or other organization, indicate the Item Numbers of those samples being transferred; sign relinquished by, date and time, and include your affiliation.
*Important Note:
Standard Turnaround Time is 2 Weeks/10 business days. Results will be delivered by end of business on the date due unless other arrangements
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f
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vce Analytical*
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CHAIN-OF-CUSTODY / Analytical Request Document
The Chain-of-Custody is a LEGAL DOCUMENT. All relevant fields must be completed accurately.
Section B
Required Project Information:
Report To: M *.
Copy To:
, K p y jr
.. L m d s T ro m
Section C
Invoice Information: Attention:
Company Name:
NPDES UST
Page: / of j
0945966
REGULATORYAGENCY
GROUNDWATER
RCRA
DRINKING WATER & Other
Address:
Email To- i v .
s r Iia c L s V o w \ ( 8 >yitnft1. c o m
Phone
_ - _ ,, Fax
l 5 l- T ? 8 -5 3 5 *
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One Character per box. (A-Z.p-9/.-)
Samples IDs MUST BE UNIQUE
Purchase Order No.:
Project Name:
r
fe e c a itA A O u ' t A L U 001
ProjectN^ m0b^ - O 0 ^ d
Valid Matrix Codes
MATRIX
CQDE
DRINKING WATER DW
WATER
WT
WASTE WATER WW
PRODUCT
R
SOIL/SOliD
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WIPE
air
OTHER
` SL -
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WP W
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Pace Quote Reference:
'fcieYPace Project Manager:
,
F C VY\ o * \
S **rH A
Pace Profile #: ^T<"
COLLECTED COMPOSITE START COMPOSITE END/GRAB
DATE
*- Z
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SITELOCATION
GA OIL noH nsc
GIN CIMI MN CNC nwi Ntother A l A&a<*><4
Preservatives
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Additional Comments:
c. h I oa A t ' o -il '
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SEE REVERSE SIDE FOR INSTRUCTIONS
RELiNQL'ISHED BY / AFFILIATION
1 ^
3-/ISOV
SAMPLER NAME AND SIGNATURE
PRINT Name o f SAMPLER:
SIGNATURE o f SAMPLER: V
DATE Signed (M M /D D /Y Y )
_______ 2 /-5~ i ( n
ALLQ020rev.3.31 Mar05
Instructions for completing Chain of Custody (COC)
1. Section A and B: Complete all Client information at top of sheet: company name, address, phone, fax, contact (the person to contact if there are
questions, and who will receive the final report.), e-mail address (if available), PC)#. Projeet Name and/or Project Number as you would like to see it
appear on the report.
,
2. Section C: Invoice Information: Billing information is included in this section. This information should include the name and address of the person
receiving the invoice.
3. Quote Reference should be completed if a quotation was provided by Pa^jj; Analytical. The Project Manager, and Profile No. will be completed by
Pace Analytical Services.
'
4c'*'
'' '
'
.
.' -.' '3
'.
4. Site Location: A separate COC must be filled out for each day ofsigriple'collection. Record the two letter postal code for the US state in which the
samples were collected.
',
5. Regulatory Agency: List the program that is guiding the work to ensure proper regulations are followed.
6. Section D : Complete a Sample Description in the "SAMPLE ID' section as you would like it to appear on the laboratory report. The following information should also be included: the sample matrix, sample type (G (grab) or C (composite). When collecting a composite, the start time and end
- time should be documented in the respective boxes. The collection time for a grab (G) sample should be entered in the boxes marked 'Composite End/Grab'), Sample temp at collection (if required by state), the total number of containers, and preservative used. '
7. Mark if the sample was filtered in the field by marking Y or N in 'Filtered' row by the Analysis requested.
.
8. Requested Analysis: List the required analysis and methods on the lines provided and place a check in the column for the samples requiring the analysis. Additional comments should be referenced in the bottom left hand comer or include attachments for extended lists of parameters.
. 9. The sampler should print their name in the space provided and sign their name followed by the date of the sampling event at the bottom of the COC in
the spaces designated for `SAMPLER NAME AND SIGNATURE'.
' '`
.
10. When relinquishing custody of the samples to a representative of the laboratory or other organization, indicate the Item Numbers of those samples
being transferred; sign relinquished by, date and time, and include your affiliation.
:
*Important Note:
j
Standard Turnaround Time is 2 Weeks/10 business days. Results will be delivered by end o f business on the date due unless other arrangements
have been made with your project manager. \ . . :
,
Special Project Requirements such as Low Level Detection Limits or level of QC reported must be included on the chain of custody in the Additional Comments section.
CHAIN-OF-CUSTODY / Analytical Request Document
ace Analytical'
/Section A
' Required Client Information:
Section B
Required Project Information:
The Chain-of-Custody is a LEGAL DOCUMENT. All relevant fields must be completed^ccurately.
Section C
Invoice Information:
Page: ( of ]
0945966
Company --.
3m Address
, Report To:
f r j i i __________
fY L .
1 Copy To:
P O T L u n d s T ro m
Attention: Company Name:
NPDES UST
REGULATORY AGENCY
GROUNDWATER
DRINKING WATER
RCRA
& Other
Email To- i i i
,,
n t li^ o < V o w
c o v r\
Purchase Order No.:
Address: Pace Quote Reference:
SITE LOCATION
GA D IL G IN GMI MN GNC OH GSC GW I V^oTHER A t - A B A * / ?
PhoneU 5 i - l l d ~ S__i_5,A Fax
Requested Due Date/TAT:
Project Name:
r
Pace Project Manager:
,.
f e c c a W O u H a L U 001 F C -W to m ,
T t c Y S w n t-IA
Project N^mb^r: ,,
^
Pace Profile #:
^
S e c t i o n D Required Client Information
SAMPLE ID
One Character per box. (A-Z,p-9/.-) :
Samples IDs MUST BE UNIQUE
Valid Matrix Codes
MATRIX
CODE
DRINKING WATER DW
WATER
WT
WASTE WATER WW
PRODUCT
P
SOIL/SOLlD
. SL
o il >
o i-^ rr t
WIPE
WP 3
AIR AR i ^ | j
OTHER
OT Y
TISSUE
TS 4 * '
>*v e>
o h- ti mO COLLECTED
5
LU h I- O
LU y
COMPOSITE START COMPOSITE END/GRAB DATE
* h y/oc, i ^ v
A
Ou-V A WW o o \
a vu 0>l
i l l u *-n
O vft jp -v u O O \ 1r f f . 0 1 E 5 DU
0
oc I
ioO p?ib V^k
I ID C
W :T ra .v l B l,c k _
B FU>
u0 * ' w,
Vi St
B f ill
(>Vf I h U V = ,H p
tyUj
?337? W U
2 2 WW
f
WT
7 2 3 ( UfT
; v s >//<')VO U i v r = A v l<9Q / V i
a/'rr/oc A/.y to
/o u 5 MMB iw S
V /V / i * h s h &
->/'5' oie
ItSk'OKe
>% 0 ( /
Additional Comments: c h J&/. A t , ' 0
h 'o v S s
&><nb
it
RELINQUISHED BY/AFFILIATION DATE TIME I
tl'.oO
iiim im iiu m
AACCCCEEPPTTED BY / AFFILIATION \ DATE | TIME
02/'-'< / i n
c U 'tK .M : 0 . 0 > c o~pci4/
c k lo r.w t -
SEE REVERSE SIDE FOR INSTRUCTIONS
r . . .0
ii/rS O'* e j
3
SAMPLER NAME AND SIGNATURE
JPRINT Name of SAMPLER:
or. V
, ih e /]
i /. rf,1 SIGNATURE of SAMPLER: \
...
.v V
I WA_ - W --------- -----------------------
-r;
---------------------
DATE Signed (M M /D D /Y Y )
-^ 5 /DCo
MPLE CONDITION z ?
z
<D o
csr =o
>o. O-o
ALLQQ20rev.3,31Mar05
Instructions for completing Chain of Custody (COC)
1. Section A and B: Complete all Client information at top of sheet: company name, address, phone, fax, contact (the person to contact if there are questions, and who will receive the final report.), e-mail address (if available), PO#, Project Name and/or Project Number as you would like to see it appear on the report.
2. Section C: Invoice Information: Billing information is included in this section. This information should include the name and address of the person receiving the invoice.
3. Quote Reference should be completed if a quotation was provided by Pace Analytical. The Project Manager, and Profile No. will be completed by Pace Analytical Services.
4. Site Location: A separate COC must be filled out for each day of sample collection. Record the two letter postal code for the US state in which the samples were collected.
5. Regulatory Agency: List the program that is guiding the work to ensure proper regulations are followed.
6. Section D: Complete a Sample Description in die ` SAMPLE ID' section as you would like it to appear on the laboratory report. The following information should also be included: the sample matrix, sample type (G (grab) orC (composite). When collecting a composite, the start time and end time should be documented in the respective boxes. The collection time for a grab (G) sample should be entered in the boxes marked 'Composite End/Grab'), Sample temp at collection (if required by state), the total number of containers, and preservative used.
7. Mark if the sample was filtered in the field by marking Y or N in `Filtered' row by the Analysis requested.
8. Requested Analysis: List the required analysis and methods on the lines provided and place a check in the column for the samples requiring the analysis. Additional comments should be referenced in the bottom left hand comer or include attachments for extended lists of parameters.
9. The sampler should print their name in the space provided and sign their name followed by the date of the sampling event at the bottom of the COC in
the spaces designated for `SAMPLER NAME AND SIGNATURE '.
'
10. When relinquishing custody of the samples to a representative of the laboratory or other organization, indicate the Item Numbers of those samples being transferred; sign relinquished by, date and time, and include your affiliation.
Important Note:
Standard Turnaround Time is 2 Weeks/10 business days. Results will be delivered by end of business on the date due unless other arrangements have been made with your project manager.
Special Project Requirements such as Low' Level Detection Limits or level of QC reported must be included on the chain of custody in the Additional Comments section.
ace Analytical-
/Section A
' R e q u ire d Client Information:
Company
fr jj^
Address
iC r
W tV n
com
Phone /5 1
. , , , , -, Fax
R e q u e s te d D u e Date/TjT: v "W
\
-
S A IV ^P U E ID
*\
One Character per box.
\ , 4% (Ar/.<?-9M `
TV; Sarripfes IDs MUST BE UNIQUE
E F phui
A ''S lA n Y -
CHAIN-OF-CUSTODY / Analytical Request Document
The Chain-of-Custody is a LEGAL DOCUMENT. All relevant fields must be completed accurately.
Section B
R e q u ir e d Project Information:
Report To:
1
f> 1 v. L B * V T
Copy To:
1 t1
U iy '^ s ir o m
Section C
Invoice Information: Attention:
Company Name:
Address:
Purchase Order No.:
Pace Quote Reference:
Project Name:
r
Pace Project Manager'
f e jc r iW v O B 'A L L - O O l V c W t 0 *a
Project
'
Valid Matrix Codes
MATRIX
CODE
DRINKING WATER DW
WATER
WT
WASTE WATER PRODUCT SOIL/SOLI0 OIL V WIPE AIR
OTHER TISSUE
WW P v SL ' OL `Z r f S WP ^ AR u t r &
t sT &
< - Pace Profile #:
So
$ COLLECTED
8top COMPOSITE START COMPOSITE END/GRAB
TIME
DATE
.,
2 t--o 3O li?
o<
o
o
73! >82 v r Or,
y' .v-o-vli
NPDES UST
Page: / of f
0945966
REGULATORY AGENCY
GROUND WATER RCRA
D R IN K IN G W ATE R M o th e r
S IT E L O C A T IO N
G A D IL
noH nsc
D IN
nwi
D M I MN D N C B other A l a e a ^ A
P re s e rv a tiv e s
Project Number Lab I.D
O s fr f> \V O
CO
l U P /,
A L U oo\ E f i u <"V1 Pup
o c \ t l lOVpe CcuS )
A \ O i l I E f t M PPp V-iqi>
.7M S u*w
o ^ s
n .m
i r . r i i M U C-
/-a v ;;
w w * //< / 1' '
0^> QMA.
J ' <>
H k, I
\o h 5
tons
_EI c B rj.
B f uO
D o H 4 TLor t SI. k _
l i T V s/e 1
-I
ru I f r r A t/t
l . WrA
< ? ? ? ? VvT wr
"V'T B
is r,
\
----- 1______ 1______ 1______ 1______ 1______ i-- __1______1 1 1-----1___ L 1 -1 1 -1
Additional Comments:
c M t ' . /U r
, /- Z1 1-
1 C> ( a 0
! ; >' !; O
RELINQUISHED BY/AFFILIATION DATE! TIME
C*f. :
Vj
C {/I ' t j
- 0 .
c o ^ p o iiV
^ \V
j i i
V C -H u
;
ACCEPTED BY / AFFILIATION
/ ---------
I DATE I TIME
7------------ -------
V/
(//!(. -
/ '-
SAMPLE CONDITION
zZ
>?
zz
?>
z , z
??
zz
>?
z
?
z
?
z
?
z
>
Temp in C Received on Ice Custody Sealed Cooler Samples Intact
- OC
`. I l
- ]r . S
' ' y ' Cj ,>
SAMPLER NAME AND SIGNATURE
1PRINT Name o f SAMPLER:
\ //
s
-1
~~~X
;
j
/
^-
-- * _____ W ^ ' c v . L . / ' /
=.
SEE REVERSE SIDE FOR INSTRUCTIONS
SIGNATURE of SAMPLER: \ /
v
O.
. / S -V --
.....
DATE Signed (MM / DD / YY)
-- "i
1
ALLQQ20rev.3,3t Mar05
Instructions for completing Chain of Custody (COC)
i
1. Section A and B: Complete all Client information at top of sheet: company name, address, phone, fax, contact (the person to contact if there are questions, and who will receive the final report.), e-mail address (if available), PO#. Project Name and/or Project Number as you would like to see it appear on the report.
2 Section C: Invoice Information: Billing information is included in this section. This information should include the name and address of the person
receiving the invoice.
3. Quote Reference should be completed if a quotation was provided by Pace Analytical. The Project Manager, and Profile No. will be completed by Pace Analytical Services.
4. Site Location: A separate COC must be filled out for each day of sample collection. Record the two letter postal code tor the US state in which the samples were collected.
5. Regulatory Agency: List the program that is guiding the work to ensifre proper regulations are followed.
, .*
m
6. Section D: Complete a Sample Description in the "SAMPLE ID' section as you would like it to appear on the laboratory' report. The following .
information should also be included: the sample matrix, sample type (G (grab) or C (composite). When collecting a composite, the start time atxd end
time should be documented in the respective boxes. The collection time for a grab (G) sample should be entered in the boxes marked "Composite
End/Grab'), Sample temp at collection (if required by state), the total number of containers, and preservative used.
(
7. Mark if the sample was filtered in the field by marking Y or N in Filtered' row by the Analysis requested.
8. Requested Analysis: Last the required analysis and methods on the lines provided and place a check in the column tor the samples requiring the analysis. Additional comments should be referenced in the bottom left hand comer or include attachments for extended lists of parameters.
9. The sampler should print their name in the space provided and sign their name followed by the date of the sampling event at the bottom of the COC in
the spaces designated for `SAMPLER NAME AND SIGNATURE'.
'
10. When relinquishing custody of the samples to a representative of the laboratory or other organization, indicate the Item Numbers of those samples being transferred; sign relinquished by, date and time, and include your affiliation.
^Important Note:
Standard Turnaround Time is 2 Weeks/10 business days. Results will be delivered by end of business on the date due unless other arrangements have been made with your project manager.
Special Project Requirements such as Low Level Detection Limits or level of QC reported must be included on the chain of custody in the Additional Comments section.
2/1/2006 Project: E06-0094
3M ENVIRONMENTAL LABORATORY Preliminary/Unauthorized Report
Page 1 of 4
Requester: Schnobrich, Dana M (223-1N-08) Department: 530711 Project Number: 0022674449 Date Received: 1/31/2006
Project Description: Decatur Outfall 001 FC Monitoring Quarterly
Comments:
Completion Date:
Project Lead: Kent Lindstrom Phone Number: 651-778-5352 Email Address: krlindstrom@mmm.com
Statement o f Accuracy: _____________________________________________
Project Results/Activitv Pace Field Sampling Event
3M Sample Number_____ Sampled Date______Sample Description_____________________________________
E06-0094-93375
2/14/2006
Outfall 001 Effluent - Composite
LAB EXYGEN
Analytical Method LCMS
E06-0094-93376
2/14/2006
Components PFOS
Result
PFHS PFBS
FOSA PFBAmide MeFBSE-OH
C4 acid
C5 acid C6 acid C7 acid PFOA C9 acid CIO acid
C ll acid C12 acid
Outfall 001 Effluent - Composite Duplicate
RL Qualifier
LAB EXYGEN
Analytical Method LCMS
Components PFOS PFHS PFBS FOSA PFBAmide MeFBSE-OH C4 acid C5 acid C6 acid C l acid PFOA C9 acid CIO acid C ll acid C12 acid
Result
RL Qualifier
0012
2/1/2006
3M ENVIRONMENTAL LABORATORY Preliminary/Unauthorized Report
Project: E06-0094 (cont.) 3M Sample Number_____ Sampled Date______Sample Description_________________________
E06-0094-93377
2/14/2006
Outfall 001 Effluent Comp -1 0 PPB Low Spike
LAB EXYGEN
Analytical Method LCMS
E06-0094-93378
2/14/2006
Components PFOS PFHS PFBS FOSA PFBAmide MeFBSE-OH C4 acid C5 acid C6 acid C7 acid PFOA C9 acid CIO acid C ll acid C12 acid
Result
Outfall 001 Effluent Comp -100 PPB High Spike
RL
LAB EXYGEN
Analytical Method LCMS
E06-0094-93379
2/14/2006
Components PFOS PFHS PFBS FOSA PFBAmide MeFBSE-OH C4 acid C5 acid C6 acid C7 acid PFOA C9 acid CIO acid C ll acid C12 acid
Field Control/Travel Blank
Result
RL
LAB EXYGEN
Analytical Method LCMS
Components PFOS PFHS PFBS FOSA PFBAmide MeFBSE-OH C4 acid C5 acid C6 acid C7 acid PFOA
Result
RL
0013
Page 2 of 4 Q ualifier
Q u alifier
Qualifier
2/1/2006
3M ENVIRONMENTAL LABORATORY Preliminary/Unauthorized Report
Project: E06-0094 (cont.) 3M Sample Number_____ Sampled Date______Sample Description_________________
E06-0094-93379 (cont.) 2/14/2006
Field Control/Travel Blank
LAB EXYGEN
Analytical Method LCMS (cont.)
E06-0094-93380
2/14/2006
Components C9 acid CIO acid C ll acid
Result
C12 acid
Field Control/Travel Blank Low Spike
LAB EXYGEN
Analytical Method LCMS
E06-0094-93381
2/14/2006
Components PFOS PFHS
Result
PFBS FOSA PFBAmide MeFBSE-OH C4 acid C5 acid C6 acid C7 acid PFOA
C9 acid CIO acid C ll acid C12 acid
Field Control/Travel Blank High Spike
LAB EXYGEN
Analytical Method LCMS
E06-0094-93382
2/14/2006
LAB EXYGEN
Analytical Method LCMS
Components PFOS PFHS PFBS FOSA PFBAmide MeFBSE-OH C4 acid C5 acid C6 acid C7 acid PFOA C9 acid CIO acid C ll acid C12 acid
Equipment Blank
Components PFOS PFHS PFBS FOSA PFBAmide
Result Result
0014
Page 3 of 4 RL Qualifier RL Qualifier
RL Qualifier
RL Qualifier
2/1/2006
3M ENVIRONMENTAL LABORATORY Preliminary/Unauthorized Report
Project: E06-0094 (cont.) 3M Sample Number______ Sampled Date______Sample Description
E06-0094-93382 (cont.) 2/14/2006
Equipment Blank
LAB EXYGEN
Analytical Method LCMS (cont.)
Components MeFBSE-OH C4 acid C5 acid C6 acid C7 acid PFOA C9 acid CIO acid C ll acid C12 acid
Result
Page 4 of 4 RL Qualifier
0015
Sam ple.SaTest.Test_ Test.Replie Test.Analy! ResultNan Result.Res Result.Entr Result.Attri Result.Unit
93375 985370
1 LCMS WVPFOS
N
NG/ML
93375 985370
1 LCMS_WV PFHS
N
NG/ML
93375 985370
1 LCM SJ/W PFBS
N
NG/ML
93375 985370
1 LCMS_WV FOSA N
NG/ML
93375 985370
1 LCMS_WV PFBAmide N
NG/ML
93375 985370
1 LCMS_WV MeFBSE-C N
NG/ML
93375 985370
1 LCMS WV C4 acid N
NG/ML
93375 985370
1 LCMS_WV C5 acid N
NG/ML
93375 985370
1 LCMS_WV C6 acid N
NG/ML
93375 985370
1 LCMS_WV C7 acid N
NG/ML
93375 985370
1 LCMS WVPFOA N
NG/ML
93375 985370
1 LCMS_WVC9 acid N
NG/ML
93375 985370
1 LCMS WVC10 acid N
NG/ML
93375 985370
1 LCMS_WVC11 acid N
NG/ML
93375 985370
1 LCMS_WV C12 acid N
NG/ML
93376 985371
1 LCMS_VW PFHS
N
NG/ML
93376 985371
1 LCMS WV PFBS
N
NG/ML
93376 985371
1 LCMS WV FOSA N
NG/ML
93376 985371
1 LCMS WV PFBAmide N
NG/ML
93376 985371
1 LCMS_WV MeFBSE-C N
NG/ML
93376 985371
1 LCMS_VWC4 acid N
NG/ML
93376 985371
1 LCMS_WV C5 acid N
NG/ML
93376 985371
1 LCMS_WVC6 acid N
NG/ML
93376 985371
1 LCMS_WV C7 acid N
NG/ML
93376 985371
1 LCMS_WV PFOA N
NG/ML
93376 985371
1 LCMS_VW C9 acid N
NG/ML
93376 985371
1 LCMS_WV C10 acid N
NG/ML
93376 985371
1 LCMS_WVC11 acid N
NG/ML
93376 985371
1 LCMS VWC12 acid N
NG/ML
93376 985371
1 LCMS WVPFOS
N
NG/ML
93377 985372
1 LCMS_WV PFOS
N
NG/ML
93377 985372
1 LCMS_WV PFHS
N
NG/ML
93377 985372
1 LCMS_WV PFBS
N
NG/ML
93377 985372
1 LC M SJ/W FOSA
N
N G /M L
93377 985372
1 LCMS WV PFBAmide N
NG/ML
93377 985372
1 LCMS_WV MeFBSE-C N
NG/ML
93377 985372
1 LCMS_WV C4 acid N
NG/ML
93377 985372
1 LCMS_WV C5 acid N
NG/ML
93377 985372
1 LCM SJ/W C6 acid N
NG/ML
93377 985372
1 LCMS_VW C7 acid N
NG/ML
93377 985372
1 LCMS WVPFOA
N
NG/ML
93377 985372
1 LCMS_WVC9 acid N
NG/ML
93377 985372
1 LCM SJ/W C10 acid N
NG/ML
93377 985372
1 LCMS VWC11 acid N
NG/ML
93377 985372
1 LCMS VWC12 acid N
NG/ML
93378 985373
1 LCMS WVPFOS
N
NG/ML
93378 985373
1 LCMS WV PFHS
N
NG/ML
93378 985373
1 LCM SJ/W PFBS
N
NG/ML
93378 985373
1 LCM SJ/W FOSA N
NG/ML
93378 985373
1 LCMS WV PFBAmide N
NG/ML
93378 985373
1 LCMS VW MeFBSE-C N
NG/ML
93378 93378 93378 93378 93378 93378 93378 93378 93378 93379 93379 93379 93379 93379 93379 93379 93379 93379 93379 93379 93379 93379 93379 93379 93380 93380 93380 93380 93380 93380 93380 93380 93380 93380 93380 93380 93380 93380 93380 93381 93381 93381 93381 93381 93381 93381 93381 93381 93381 93381 93381 93381
985373 985373 985373 985373 985373 985373 985373 985373 985373 985374 985374 985374 985374 985374 985374 985374 985374 985374 985374 985374 985374 985374 985374 985374 985375 985375 985375 985375 985375 985375 985375 985375 985375 985375 985375 985375 985375 985375 985375 985376 985376 985376 985376 985376 985376 985376 985376 985376 985376 985376 985376 985376
1 LCMS_WV C4 acid N
1 LCMS WV C5 acid N
1 LCMS_WV C6 acid N
1 LCMS_WV C7 acid N
1 LCMSJWV PFOA N
1 LCMS WV C9 acid N
1 LCMS_VW C10 acid N
1 LCMS_WV C11 acid N
1 LCMS_WV C12 acid N
1 LCMS_WV PFOS
N
1 LCMS WVPFHS
N
1 LCMS_VW PFBS
N
1 LCMS_WV FOSA N
1 LCMS WV PFBAmide N
1 LCMS_WV MeFBSE-C N
1 LCMS WV C4 acid N
1 LCMS_WV C5 acid N
1 LCMS_WV C6 acid N
1 LCMS_WV C7 acid N
1 LCMS WV PFOA N
1 LCMS WV C9 acid N
1 LCMS WV C10 acid N
1 LCMS VWC11 acid N
1 LCMS WV C12 acid N
1 LCMS_WV PFOS N
1 LCMS_WV PFHS
N
1 LCMS_WV PFBS
N
1 LCMS_WV FOSA N
1 LCMS_WV PFBAmide N
1 LCMS_WV MeFBSE-C N
1 LCMS_VW C4 acid N
1 LCMS WV C5 acid N
1 LCMS_WV C6 acid N
1 LCMS_WV C7 acid N
1 LCMS WV PFOA
N
1 LCMS WV C9 acid N
1 LCMS_WVC10 acid N
1 LCMS_WV C11 acid N
1 LCMS WV C12 acid N
1 LCMS_WV PFOS N
1 LCMS WVPFHS
N
1 LCMS_WV PFBS
N
1 LCMS_WV FOSA N
1 LCMS_WV PFBAmide N
1 LCMS_WV MeFBSE-C N
1 LCMS_WV C4 acid N
1 LCMS_WV C5 acid N
1 LCMS_WV C6 acid N
1 LCMS_VW C7 acid N
1 LCMS_WV PFOA N
1 LCMS_WV C9 acid N
1 LCMS WVC10 acid N
0017
NG/ML NG/ML NG/ML NG/ML NG/ML NG/ML NG/ML NG/ML NG/ML NG/ML NG/ML NG/ML NG/ML NG/ML NG/ML NG/ML NG/ML NG/ML NG/ML NG/ML NG/ML NG/ML NG/ML NG/ML NG/ML NG/ML NG/ML NG/ML NG/ML NG/ML NG/ML NG/ML NG/ML NG/ML N G /M L NG/ML NG/ML NG/ML NG/ML NG/ML NG/ML NG/ML NG/ML NG/ML NG/ML NG/ML NG/ML NG/ML NG/ML NG/ML NG/ML NG/ML
93381 93381 93382 93382 93382 93382 93382 93382 93382 93382 93382 93382 93382 93382 93382 93382 93382
985376 985376 985377 985377 985377 985377 985377 985377 985377 985377 985377 985377 985377 985377 985377 985377 985377
1 LCMS_WVC11 acid N
1 LCMS_WV C12 acid N
1 LCMS_WV PFOS N
1 LCMS_WV PFHS
N
1 LCMS WVPFBS
N
1 LCMS WVFOSA N
1 LCMS WV PFBAmide N
1 LCMS_WV MeFBSE-C N
1 LCMS_WV C4 acid N
1 LCMS_WV C5 acid N
1 LCMS WV C6 acid N
1 LCMS_WV C7 acid N
1 LCMS_WV PFOA N
1 LCMS WV C9 acid N
1 LCMS WVC10 acid N
1 LCMS_WV C11 acid N
1 LCMS WVC12 acid N
NG/ML NG/ML NG/ML NG/ML NG/ML NG/ML NG/ML NG/ML NG/ML NG/ML NG/ML NG/ML NG/ML NG/ML NG/ML NG/ML NG/ML
Result.Attri Result.Has Attributes
0019
0020
0021
1 From
USAirbill
Express
Date 3 / K I O ( &
540
DETl
Recipient's Copy
4a Express Package Service To add SATURDAY D e lh e iv .n a S a c tio n S . Packagesup to 150lbs.
* f t M M locations.
dEx Priority Overnight
.Next business morning*
[" I FedEx Standard Overnight
1-- 1 Next business afternoon*
I 1 FedEx FirstOvernight
1-- I EEaarrlileiessttnneexxtbt buussinineessssmmoomrniningg
deliveryto select locations *
Name8" 5 Company
X . ( 0 ^ , ^ l \ l g V______________ Phone .? 0 S
'P A i F .
A t i ^ 1,^ H (r. \
.r-M \h( r s
c ._______
Address
I DO
V a UA
city
2 YourInternal Billing Reference
i jA \ )P V \U t .
:r State A l Q ZIP
,b
Oept/Hoer/Suite/Room
2 6^
3 To
Recipient's Name
1 *0 k
F lq k P r ^
Phone O
? I-
Company
yy jjrv i
Recipient's
Address
3p5 8
We cannot deliver to P.0I.. boSC er P.0, ZIP c o d e s > ^
__ H l w -p
Dept/Fkwr/Suite/Room
m iU lQ M To request a package be held at ai specific FedEx location, print FedEx address here.
efe ,' > 4 a V --
* ^ -j
State P A
ZIP i l ^ - g o i
'
L
8540 9649 0291
SSSSL^
S & Saver
FedEx Envelops rate not available. Minimum charge: One-pound rate.
4b Express FreightService addTo Sa t u r d a y D o im y ,s s a c io a S .
Package*m ar150lbs.
FedEx IDajyi Freight* Next business oay.** C e lfo rC t
I I FedEx2Day Freight
I-- I Second business day.
5 Packaging
I I FedEx Envelope*
I I FedExPak*
P ] FedEx
Inekides FedEx Small Pak.
BOX
FedExLarge Pak, and FedEx Sturdy Pak.
* Declared value limit$500.
Q FedEx Tube
^^thei
6 Special Handling
I-- | SATURDAYOeSven
I Available ONLYfor FedEx Pri 1-----1 Overnight, cFe.ddEr,,x-2w0-i_ay,cFrefCdEx
I Day. Frei,ght, and FedEx2Day. Freightto selectZIP codes.
lactuda FedEx address m Seetien 3.
j-j HOpSatorday 1w u u / w w w M y at FedEx Location
a t FedEx Location
Not available for
Available ONLYfor FedEx Priority
FedEx FirstOvernight
Overnightand FedEx2Dey
to select locations.
Doesthis shipment containdangerousgoods?
YesOee box mustbe checked.
'No n Yes
n
I___..I...A..s...p..e..r. a.t.ta.c.h.ed
I___I Sh.ip.pe.r's. Declaration
/\
Shipper's Dectorrion.
not required,
^a n g e ro u s goods (including dry ice) cannotbe shipped in FedEx packaging.
I I Dry Ice
I-- 1 Dryviicce,.99.,1UN 1845 -
I I Cargo Aircraft Only
7 Payment Biuta: - EuterFedExAcciNo.orCreditCardNo.below.
te tfe
CU Recipient Q Third Party Q CreditCard
Obtain Recip.l I AeM kli-i ^------
0 CastyCheck
m Total Packages
\
- ' -
TeelW wght
.
TotalDoctaredV oter
Total Charges
1
------------------------------------
-------------------------- c----------
$
.00
tQur liability is limited to $100 unless you declare a higher value. See back fo r details.
1 Credit Card Auth.
8 NEW Residential Delivery Signeture Options If you requirea signature, check Director Indirect
I-- , No Signature
, Direct Signature !-- , Indirect Signature
RfiOUired
Anyone at recipient's
at| If no one is available
I-----' Package may be left with `---- i ardirdireasusIYm1aAyVssiugmn ffonrrHdealivuemryv.. '----- ' rreocriinpiiaeRntt''ssaaddddrreessss.-,-aannuynonnee -
out obtaining a signature frdetvety.
at a neighboring address may signfor delivery, fe e y f ,:~
Rev. Date 5/QSPart #158281< 994-2005 FedExPfflNTED IN U S A SRY
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