Document v15qwyvE19x89XLrda1VNjz1b

BACK TO MAIN Centre Analytical Laboratories, Inc. 3048 Research Drive State College, PA 16801 www.centrelab.com ^P h on e : (814) 231 -8032 Fax: (814) 231 -1253 or (814) 231 -1580 Analytical Report Fluorochemical Characterization of Drinking Water Samples Port St. Lucie, FI (W2363) Centre Analytical Laboratory Report No. 023-007E (Revision 1) Revision Date 3/20/01 Testing Laboratory Centre Analytical Laboratory, Inc. 3048 Research Drive State College, PA 16801 3M Environmental Laboratory Contact Kent R. Lindstrom Bldg. 2-3E-09 P.O. Box 33331 St. Paul, MN 55133-3331 Phone: (651)778-5352 Requester Kris J. Hansen, Ph.D. 3M Environmental Technology & Safety Services Bldg. 2-3E-09 P.O. Box 33331 St. Paul, MN 55133-3331 PAGE 1 0 F 5 BACK TO MAIN 1 Introduction Results are reported for the analysis of a series of drinking water samples received by Centre Analytical Laboratories, Inc. (Centre) from the 3M Environmental Laboratory. The samples were collected from Port St. Lucie, FI. The Centre study number assigned to the project is 023-007. Specific fluorochemical characterization by liquid chromatography / tandem mass spectrometry (LC/MS/MS) was requested for all samples. A total of 16 samples 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 Perfluorooctane Sulfonate Perfluorooctane Sulfonvlamide Perfluorooctanoate Acronvm PFOS PFOSA POAA The analytical method used was validated by Centre. The validation protocol and results are on file with Centre. Data presented here is the highest quality data available at this time. 2 Sample Receipt The samples were submitted in individual plastic containers and were not preserved. Sixteen individual sample containers were received. Samples were received on 02/15/00. The sample collection dates were not supplied. Chain-of-custody information is presented in Attachment C. 3 Holding Times The analytical method used was validated against a maximum holding time of 14 days. The stability of the analytes of interest for longer periods has not been determined. However, it should be noted that field fortifications in water and other matrices have shown acceptable recoveries at 100 and 1000 ng/L for periods longer than 14 days. PAGE2 OF5 BACK TO MAIN 4 Methods - Analytical and Preparatory 4.1 LC/MS/MS 4.1.1 Sample Preparation for LC/MS/MS Analysis 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 forty-milliliter portion of sample was transferred to a C18SPE cartridge. The cartridge was first eluted with 5 mL of 40% methanol in water solution. The eluate was discarded and the SPE column was then eluted with 100% methanol. A 5 ml portion of methanol was collected for analysis by LC/MS/MS. This treatment resulted in an eight-fold concentration of the 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 fluorochemicals. Electrospray is generally operated at relatively mild temperatures; molecules are ionized, fragmented, and detected. Ions characteristic of known fluorochemicals are observed and quantitated against standards. A Hewlett-Packard HP1100 HPLC system coupled to a Micromass Ultima MS/MS was used to analyze the sample extracts. Analysis was performed using selected reaction monitoring (SRM). Samples were extracted on 2/25/00 and analyzed by MS/MS on 2/26/00. The HPLC and MS/MS methods used for analysis and instrument parameters can be found in attachment D. 5 Analysis 5.1 Calibration A 7-point calibration curve was analyzed at the beginning and end of the analytical sequence for the compounds of interest. The calibration points were prepared at 0, 25, 50, 100, 250, 500, and 1000 ng/L (ppt) The response of the quantitation ion 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 same SPE procedure used for samples. Calibration check standards were analyzed periodically (every three to five sample injections) throughout the analysis sequence. Compliance is obtained if the standard analyte concentrations are within +/-20% of the actual value. For the results reported here, calibration criteria were met. PAGE 3 OF 5 BACK TO MAIN 5.2 Blanks Extraction blanks were prepared and analyzed with every extraction batch of samples. The extraction blanks should not have any target analytes present at or above the concentration of the low-level calibration standard. For these samples, the extraction blanks were compliant. Instrument 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-level 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 method. 5.4 Matrix Spikes Matrix spikes were prepared for every sample at a concentration of 100 ng/L using all compounds of interest. Matrix spike recoveries are given in Attachment B. Field spikes were also prepared on several samples at a concentration of 100 ng/L using all compounds of interest. Field spike recoveries are also given in Attachment B. 5.5 Duplicates All samples were analyzed in duplicate. Results are given along with the sample results in Attachment A. 5.6 Laboratory Control Samples Milliq water was spiked with all compound of interest at 25 and 250 ng/L. All recoveries for all compounds were between 70-130% in each LCS. 5.7 Sample Related Comments Field blank samples consisted of empty containers. Forty milliliters of type I water filtered through a hypercarb cartridge was added to the empty container and analyzed in the same manner as the other samples. 6 Data Summary Please see Attachment A for a detailed listing of the analytical results. 7 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 Centre. PAGE 4 OF 5 BACK TO MAIN 8 Attachments 8.1 Attachment A: Results 8.2 Attachment B: Matrix Spike Recoveries (Field and Laboratory Spikes) 8.3 Attachment C: Chain of Custody 8.4 Attachment D: LC/MS/MS Raw Analytical Data 9 Signatures Other Lab Members Contributing to Data Enaksha Wickremesinhe Karen Smith PAGE 5 OF5 BACK TO MAIN _ ANALYTICAL REPORT Analytical Results W2363 Port St. Lucie, FI 3M Sample Identification MC-615H MC-617H MC-620H MC-621H MC-623H MC-626H MC-628H MC-631H NA MC-632H NA MC-633H Sample Description Intake-P/N Intake-P/N duplicate Intake-Field Blank Empty Outflow-P/N Outflow-P/N duplicate Site 1 P/N Site 1 P/N duplicate Site 2 P/N Site 2 P/N duplicate Site 3 P/N Site 3 P/N duplicate Field Blank-P/N Empty PFOS (ng/L) ND ND ND ND ND ND ND ND ND ND . ND ND PF( (ng/L) ND ND ND ND ND ND ND ND ND ND ND ND POAA (ng/L) ND ND ND ND ND ND ND ND ND ND ND ND Limit of Detection (LOD) for the procedure Is appoxlmately 2.5 ng/L for PFOS and PFOSA and 7.5 ng/L for POAA Limit of Quantitation (LOQ) for the procedure Is 25 ng/L for all compounds ND - Compound not detected NQ - Compound detected at a level between the LOD and LOQ. Result is not quantifiable. ND < LOD < NQ < LOQ Please refer to the reverse side for our standard terms and conditions. 0 BACK TO MAIN Attachment B: LC/MS/MS Laboratory Spike Recovery Sample 10: Spiked Amount (ng/L): MC-619H 100 PFOS PFOSA POAA Lower Recovery Limit: Upper Recovery Limit: Sample Concentration (ng/L) 0 0 0 70 130 Matrix Spike Result (ng/L) 87.1 90.4 96.2 Matrix Spike Result (% Recovery) 87.1 90.4 96.2 Criteria (Pass / Fail) PASS PASS PASS BACK TO MAIN Attachment B: LC/MS/MS Laboratory Spike Recovery Sample ID: Spiked Amount (ng/L): MC-625H 100 PFOS PFOSA POAA Lower Recovery Limit: Upper Recovery Limit: Sample Concentration (ng/L) 0 0 0 70 130 Matrix Spike Result (ng/L) 83.6 89.5 93.2 Matrix Spike Result (% Recovery) 83.6 89.5 93.2 Criteria (Pass / Fail) PASS PASS PASS BACK TO MAIN Attachment B: LC/MS/MS Laboratory Spike Recovery Sample ID: Spiked Amount (ng/L): MC-630H 100 PFOS PFOSA POAA Lower Recovery Limit: Upper Recovery Limit: Sample Concentration (ng/L) 0 0 0 70 130 Matrix Spike Result (ng/L) 87.4 81.0 98.3 Matrix Spike Result (% Recovery) 87.4 81.0 98.3 Criteria (Pass / Fail) PASS PASS PASS BACK TO MAIN Attachment B: LC/MS/MS Laboratory Spike Recovery Sample ID: Spiked Amount (ng/L): MC-631H 100 PFOS PFOSA POAA Lower Recovery Limit: Upper Recovery Limit: Sample Concentration (ng/L) 0 0 0 70 130 Matrix Spike Result (ng/L) 95.0 87.0 104 Matrix Spike Result (% Recovery) 95.0 87.0 104.0 Criteria (Pass / Fail) PASS PASS PASS BACK TO MAIN Attachment B: LC/MS/MS Laboratory Spike Recovery Sample ID: Spiked Amount (ng/L): MC-632H 100 PFOS PFOSA POAA Lower Recovery Limit: Upper Recovery Limit: Sample Concentration (ng/L) 0 0 0 70 130 Matrix Spike Result (ng/L) 94.0 97.1 95.8 Matrix Spike Result (% Recovery) 94.0 97.1 95.8 Criteria (Pass / Fail) PASS PASS PASS BACK TO MAIN Attachment B: LC/MS/MS Field Spike Recovery Sample ID: Spiked Amount (ng/L): MC-618H 100 PFOS PFOSA POAA Lower Recovery Limit: Upper Recovery Limit: Sample Concentration (ng/L) 0 0 0 70 130 Matrix Spike Result (ng/L) 125 128 125 Matrix Spike Result (% Recovery) 125.0 128.0 125.0 Criteria (Pass / Fail) PASS PASS PASS BACK TO MAIN Attachment B: LC/MS/MS Field Spike Recovery Sample ID: Spiked Amount (ng/L): MC-624H 100 PFOS PFOSA POAA Lower Recovery Limit: Upper Recovery Limit: Sample Concentration (ng/L) 0 0 0 Matrix Spike Result (ng/L) 128 109 126 130 Matrix Spike Result (% Recovery) 128.0 109.0 126.0 Criteria (Pass / Fail) PASS PASS PASS BACK TO MAIN Attachment B: LC/MS/MS Field Spike Recovery Sample ID: Spiked Amount (ng/L): MC-629H 100 PFOS PFOSA POAA Lower Recovery Limit: Upper Recovery Limit: Sample Concentration (ng/L) 0 0 0 70 130 Matrix Spike Result (ng/L) 130 107 126 Matrix Spike Result (% Recovery) 130.0 107.0 126.0 Criteria (Pass / Fail) PASS PASS PASS Envii .mental Laboratory Form 38778 - PWO Shipping Address: 3M Bklg 2-3E-09 935 Bush Avenue St. Paul, MN 55106 Telephone: Sample Receiving: (651) 778-4948 Alternate: (651) 778-6753 FAX: (651)778-6176 Contact Name z, ^ Company '2^Y\ BACK TO MAIN Chain of Custody /R eque^ jr Laboratory Analytical i / i J J Project ID/Project Name D P i - O l l M i > l4 n /.VLTA^tLKnlunii U J k M s A y) * L / & > Template # Fit'l l Reprt Due Date d <J Project Lead J y / js Internal Due Date Dept. # (main) / . Class/Job/Project # iQ O t S ' S O tS A Date Available 3M Env j Project # For Inteiiidl Use Only Report Results to: Mailing Address fouM 'i/W l 2 ~ ^ ~ T P \ Crty, State, Z . p < ^ . i Telephone # pOfT Special Instructions and/or Specific Regulatory Requirements: (method, limit of detection, repotting units, etc.) P O Prt)L FAX * ( k S H T 7 & - b U b (b tA ^ O \ \ Date Due Contract Lab Preservatives: ( L 1 U T <2- L . Analysis Requested: Complete below. Attach any associated Information. V ib T 'L 0Z1n ** oCXMO coa> z VOCs Other Total Number of Containers Item # Client Sample Identification 1. y M - b S F\ 2. m C -L > n iA - J v r U b - f i d ! A j u b ____________ 3. ~ T y .lA 5 > p ilL i - P / A J 4. m c -L p l^ M - ^ ) k U - U J o S p i t i -P ) M _____ 5. m o M P iH -J V v V U . -T ig -V I k ^ ilh -P lA M m fk i 6. rr\L- (p ^ \ -C tH Vfppu -P Ia J _________________ ^ 7. 8. m o / / -O H V W - T i ^ ^ p i u . - p / A j ____ 9. m o L W 5 >-) - (P ^ -v ic w -b b S p iL e . -P iA J _____ 10. M C - b ^ U U ^Lfce.L z .Ia A __________________ Collected by (print): Item # Relinquished by/Affillatlon \h o \ / j a L cm s& } u j z i j u ' j p t y y ) 3M LIMS# Date Sampled aM - Time Sampled Matrix/ Media Enter the number of containers of each P l A UJ/xA H .\ \ t l I (Enter an 'X' in the box below to indicate request) \1___ \y Vi y / i \V \J T r Collector's signature: 1 1 1 1 1 Time -- : Date Shipped Via: 7*--tl ltQ//*iT*-.* - Received bv/Affiliation ^ Time Date \0%O L-IF-Ci) Chain of Custod Sample Condition Upon Receipt: Acceptable 0 Other: Temperature: 'C Received on Ice Other Associated CoCs: l~) \ ~UO, IT t'Z.', |~J l XX\ 1*7 13, H I'iS " Copies to: m n . i m n i r t , m * o ,n > b \,n W l4 ^ }-). L A L f T P Paga i i - Of Original - Accompanying Samples Last Page - Originator Comments: See Reverse Side for Instructions 3 M Envii mental Laboratory Form 3877B - PWO .. Shipping Address: 3M Bldg 2-3E-09 935 Bush Avenue St Paul, MN 55106 Telephone: Sample Receiving: (651) 778-4948 Alternate: (651) 778-6753 FAX: (651)778-6176 BACK TO MAIN Chain of Custody /Reque.^,,. jr Laboratory Analytical 1 (1J4 Project tD/Project Name 0 2 V O C T 7 ' flfW W rV r t-lvA V d U ) r O r in y i/tA t Template # F ihil Repbrt Due Date 0 Project Lead iW lO Internal Due Date Dept. # (main) <-) / Class/Job/Project # O O t o S ^ S Q S A ^ 3M Env. >Project # For Internal Use Only Contact Name V>r i S 3 3ifl Company STA * Mailing Address p^ t- O O. City. State, Zip ^n a. Telephone# (i0^ m ^ (oOi^ Special In structions and/or Specific Regulatory Requirements: (method, limit of detection, reporting units, etc.) _ f)\ P D &UlL S S 13 5 *F A X (ifiSJ &LO -Oi[ Date Available Date Due Contract Lab ~ 11U=_____________ P re s e rv a tiv e s : c KJf _ T e t . A nalysis Requested: Complete helow. Attach any associated inform ation. Other Total Number of Containers \aJ 2 $ I p 3 SF U x i e , rL . f) o z X * o wM X 10 0) oc Oo >z Item Client Sample Identification # 3M LIMS# Date Sampled 1. - s U t cup P u M b 2. M i- b a t f - S ) b l A ^ W L S p U - P / V b3. >\ L - I p 4D -S \ U A nS W i ~Y)A) 4. k n C - U > 3 / L \ - 5 > i t r 3 - P I / O ' 5. im / - J A J- 5 ____________________________ 6. I L - [iVA-Tpi-iXA h k n h ~ P lA J / i/ T t ^ y_ i____ > N/ 7. 8. 9. -- r * ______________________ ___ 10. rr s P ^ Collected by (print): o oS3</> Item # l-(o Relinquished by/Affiliation ' i h a. C m u j J j L i / 1 3 y y ) o c <3 on Time _r___. Time Sampled 1 Matrix/ Media LM tf Enter the number of containers of each " ZI ____ / / y -y 1 \ 1 \ (Enter an X in the box below to indicate request) \J \/ 7$ VT~ :%L Collector's signature: \ \ Date Shipped Via: Received by/Affiliation fi Time Date ----- ---. ^ 1o % o Z-IS--> Sample Condition Upon Receipt: e Acceptable O Other: Temperature: Other Associated CoCs \ i7 iL 7 'C 6 Received on Ice i o , n I l i , n 1LTi n 1x 3 , m i i j Copies to; LAC/ Comments; Page Of Original - Accompanying Samples Last Page - Originator See Reverse Side for Instructions