Document VGM7xz56OVKK7z1EbXXE6RKVq

DEPARTMENT OF THE NAVY NAVAL RESEARCH LABORATORY 4SS5 O VERLO O K AVE SW W A SH IN G T O N DC 20375-5320 B t r m to 3900 Ser 6180/0047 1 9 FEB 2013 From: Commanding Officer, Naval Research Laboratory To: Deputy Under Secretary of Defense, Installations and Environment (Environmental Readiness, Safety, and International Environmental Programs - Nicholls) Subj: AUSTRALIAN DEPARTMENT OF DEFENCE AFFF INQUIRY Ref: (a) E-mail from Ms. Ninette Sadusky, OSD-ATL dtd 15 Feb 2013 (b) DoD Ltr ASEE-D/OUT/2012/AF12854190 dtd 4 Jan 2013 Enel: (1) Identification of Novel Fluorochemicals in Aqueous Film-Forming Foams Used by the U.S. Military 1. In response to references (a) and (b), the environmental impact posed by various formulations of firefighting foams has received a great deal of attention in the United States and has been an ongoing topic of discussion within the Technical Cooperation Program (TTCP) Maritime Systems Group, which includes representatives from the United States, United Kingdom, Canadian, New Zealand, and Australian governments. 2. Aqueous Film Forming Foam (AFFF) for use aboard commissioned U.S. Navy ships is required to be in accordance with military specification MIL-F-24385F. Current products are listed in the U.S. DoD qualified products database (QPD). There are no restrictions on procurement of AFFF. U.S. Navy ships are permitted to discharge AFFF under non emergency conditions for required system testing. Such discharge is only permitted in international waters; otherwise AFFF runoff must be collected for disposal. 3. The Naval Research Laboratory (NRL), located in Washington, DC, conducts all qualification testing of foams to MIL-F-24385F. In addition, NRL has conducted various research projects on AFFF and alternative foam technologies, and has a great deal of experience with the Solberg RF6 fluorine-free foam product discussed in reference (b), which was originally developed by 3M Australia. 4. Assessing the relative environmental impacts o f different foam products is complicated, as there are several different classes of possible environmental effects which are not directly comparable; a. All AFFF's (but not fluorine-free foams such as RF6) contain fluorosurfactants, which are environmental persistent as a class. As a result o f legacy AFFF use, soil and ground water at a number of present and former DoD sites in the U.S. are contaminated by fluorosurfactants. The DoD Strategic Environmental R&D Program (SERDP) has funded several research projects to characterize the types and occurrence of fluorosurfactant contamination from legacy AFFF use and to develop remediation technologies. At present, US00005830 Subj: AUSTRALIAN DEPARTMENT OF DEFENCE AFFF INQUIRY there is no straightforward treatment approach once fluorosurfactants have been dispersed into the environment. Enclosure (1) provides an example of research funded by an ongoing SERDP study that relates to the identification of fluorochemicals in AFFF used by the U.S. Military. b. Perfluorooctane sulfonate (PFOS) is a specific class o f fluorosurfactants which was manufactured by 3M and was used primarily in 3M's AFFF products. We are unaware of the presence of PFOS in any current MILSPEC AFFFs, including the Ansul products noted in reference (b). Enclosure (1) reported the presence of PFOS only in the 3M products. c. Perfluorooctanoic acid (PFOA), sometimes called "C8", is not present in MILSPEC AFFFs, but in some cases, the fluorochemical surfactants in AFFF can degrade into PFOA in the environment. The key factor for this to occur is the presence of an eight-carbon fluorinated "tail" on the surfactant molecule. The non-PFOS fluorosurfactants currently used in AFFF have predominately a six-carbon tail, which cannot form PFOA. However, they typically have an eight-carbon tail impurity. The current U.S. EPA PFOA Stewardship Program has established a goal to eliminate PFOA, PFOA precursors and related higher homologue chemicals from emissions and products including AFFF, by 2015. This will require reformulation of AFFF products and their re-qualification under the MIL-F-24385F standard. In short, current MILSPEC AFFFs do not contain PFOS, and will not contain significant materials capable of degrading into PFOA after reformulation, but they do contain fluorochemicals which are environmentally persistent. d. In addition to the long-term impact of fluorosurfactants, AFFF can have acute environmental effects. They can be acutely toxic to aquatic life forms, particularly fish. The mechanism of fish toxicity is adherence of the hydrocarbon surfactants to the fish gills, causing suffocation. Alternative fluorine-free formulations will have higher levels of hydrocarbon surfactants in comparison to AFFF and therefore may have greater fish toxicity. However, fluorine-free alternative foams will degrade quickly in the environment. There is no straightforward way to compare the relative environmental impact of short-term toxicity to that o f long-term environmental persistence. e. Because AFFF and fluorine-free foams both contain hydrocarbons, which can be biodegraded, their oxidation can cause depletion o f oxygen if large amounts are discharged into a small body of water. For this reason, MIL-F-24385F specifies a maximum chemical oxygen demand (COD) as well as a minimum ratio of biological oxygen demand (BOD) to COD. 5. With regard to Solberg RF6, previous NRL AFFF MILSPEC testing has demonstrated that the present RF6 formulation does not conform to MIL-F-24385F, and cannot be used as an AFFF substitute in U.S. DoD applications which require MILSPEC AFFF. The principal reasons for this are: 2 US00005831 Subj: AUSTRALIAN DEPARTMENT OF DEFENCE AFFF INQUIRY a. MIL-F-24385F explicitly states that AFFF must contain fluorosurfactants. In addition, it requires that all qualified products be cross-compatible (two or more qualified products mixed in any proportions must maintain the same firefighting performance). Cross compatibility with several AFFF formulations already listed on the QPD would be difficult to achieve for a fluorine-free foam. b. Although RF6 has good fire suppression performance, it falls short o f the MIL-F24385F requirements. Fire extinguishment times for RF6 against a six-foot diameter gasoline test fire (as tested by NRL) range from 35 seconds to 40 seconds, compared to a 30second maximum extinguishment time required by the MIL-F-24385F standard, and a typical extinguishment time of 23 seconds to 25 seconds for DoD qualified AFFFs. An extinguishment time as short as possible is critical for applications such as flight decks fires where there may be ordnance present. c. As presently formulated, the RF6 concentrate is very viscous, and would not be compatible with existing proportioning systems aboard U.S. Navy ships which require a low viscosity concentrate. MIL-F-24385F has a concentrate viscosity specification for this reason. 6. The Naval Research Laboratory's points of contact are John P. Farley, Code 6186, (202) 404-8459, e-mail: john.farlev@nrl.navv.mil and Dr. Bradley A. Williams, Code 6185, (202) 767-3583, e-mail: bradlev.williams@nrl.navy.mil. RICHARD J. COLTON By direction Copy to: COMNAVSEASYSCOM (Code 05P, Hunstad, Fletcher) 3 US00005832 pubs.acs.org/est Correction to Identification of Novel Fiuorochemicals in Aqueous Film-Forming Foams Used by the US Military B. J. Place and J. A. Field* Environ. Sci. Technol. 2012, 4<S(l3), 7120-7127; D O I: 10.1021/es301465n It was incorrectly written that the fluorotelomer chain lengths fycohlaratienth(leFenifggluutroherso4itdAeel)onmtwifeeirreedsu4w:le2for, ne6a:6m2:,2i,d8e:82:,2d,aimn1d0e:t2h1,y0:la2na,dmw1ihn2ee:n2.ctaAhrelbsooax,c-ttuhael fluorotelomer sulfonamide amine (Figure 4B) chain length pshaogueld71b2e4"6u:n2daenrd"N8:a2t"io. nTahlesFeoacomrrAecFtiFoFn"s should be made on and on page 7125 under "Fire Service Plus AFFF". The structure in Figure 4A should in the sSauyp"pno=rti6n,g8, 10, 12". This change should Information under Table S also be made 2 under the column "Generic Structure". In the Supporting Information on Tables SI and S2, the identified accurate masses are correct, as well as the elemental composition. This correction does not change the overall findings of the study. AUTHOR INFORMATION C*Pohrroensep:o5n4d1i-n7g37A-2u2t6h5o;re-mail: Jennifer.Field(oregonstate. Hjpr ACS Publications C 2012 American Chemical Society Published: September 17, 2012 10859 dx.doi.org/10.1021/es303627k I Environ. Sci. Technol. 2012, 46, 10859-10859 US00005833 daence&iecnnuogy pybs.acs.org/est Identification of Novel Fluorochemicals in Aqueous Film-Forming Foams Used by the US Military Benjamin J. Place* and Jennifer A. Field*'* department of Chemistry, Oregon State University, Corvallis, Oregon department of Environmental and Molecular Toxicology, Oregon State University, Corvallis, Oregon O Supporting Information ABSTRACT: Aqueous film-forming foams (AFFFs) are a vital tool to fight large hydrocarbon fires and can be used by public, commercial, and military firefighting organizations. In order to possess these superior firefighting capabilities, AFFFs contain fluorochemical surfactants, of which many of the * chemical identities are listed as proprietary. Large-scale " controlled (e.g., training activities) and uncontrolled releases of AFFF have resulted in contamination of groundwater. Information on the composition of AFFF formulations is needed to fully define the extent of groundwater contamination, and the first step is to fully define the fluorochemical composition of AFFFs used by the US military. Fast atom bombardment mass spectrometry (FAB-MS) and high resolution quadrupole-time-of-flight mass spectrometry (QTOF-MS) were combined to elucidate chemical formulas for tire fluorochemicals in AFFF mixtures, and, along with patent-based information, structures were assigned. Sample collection and analysis was focused on AFFFs that have been designated as certified for US military use. Ten different fluorochemical classes were identified in tire seven military-certified AFFF formulations and include anionic, cationic, and zwitterionic surfactants with perfiuoroalkyl chain lengths ranging from 4 to 12. The environmental implications are discussed, and research needs are identified. INTRODUCTION Aqueous film-forming foams (AFFF) formulations are chemical mixtures that are used to effectively extinguish hydrocarbon fuel-based fires and have a secondary benefit of preventing reignition.1 Due to their surface-tension lowering properties, AFFF containing fluorinated surfactants have superior fire fighting capabilities compared to nonfluorinated fire extinguish ing methods.2 Fluorinated surfactants have other unique properties that cause some of these compounds to be classified as persistent, bioaccumulative, and toxic.3 Historical reports of uncontrolled spills and the repeated use of AFFF during fire training and for AFFF performance testing have been correlated to higher concentrations of fluorochemicals, including perfiuoroalkyl carboxylates, perfiuoroalkyl sulfonates, and fluorotelomer sulfonates, in biota, surface water, or groundwater.4-8 These studies did not report the fluorochem ical composition of the AFFF released, and therefore there is no direct connection between the AFFF product spilled and the resulting contamination. The US military possesses the largest stockpile (almost 11 million liters) of AFFF in the United States, accounting for approximately 29% of all AFFF in the US in 2004.9 Unlike general commercial AFFF formulations, AFFF sold to the US military must conform to military-specific performance and quality control requirements as prescribed by the military specification (Mil-Spec) MIL-F-24385, which specifies charac teristics such as extinguishment time, corrosion rate, environ mental impact as indicated by short-term toxicity (LC50 (Fundulus herteroclitus)), biological oxygen demand (BOD), and chemical oxygen demand (COD)), and total fluorine content (no specific methodology is required).10 Nonmilitary AFFF must comply with other performance standards. Once an AFFF product has been shown to perform to MIL-F-24385 requirements, the product is listed on the US military's AFFF Qualified Products Listing (QPL). Since the initial development of AFFF materials in 1966, seven different manufacturers have developed AFFF that have passed military specifications, and a subset was purchased on contract in large quantities by the military (Figure l).1 The fluorochemicals contained in the AFFF formulations can be the result of electrochemical fluorination or telomerization processes. These AFFF formulations sold by 3M containing fluorochemicals synthesized by electrochemical fluorination accounted for 75% of the total AFFF stockpiled on military bases.9 The remaining stockpiled AFFF contain telomerizationbased fluorochemicals,9 which are structurally distinct from those made by electrochemical fluorination, a process dominated by 3M,11'12 Telomerization-based fluorochemicals possess carbon chains that are not fully fluorinated and typically have homologues of varying --C2F4-- units, while electrofluorination-based fluorochemicals possess fully fluorinated Received: April 12, 2012 Revised: June 6, 2012 Accepted: June 7, 2012 Published: June 7, 2012 -wy ACS Publications 2012 American Chemical Society 7120 dx.doi.org/!0.1021/esJ01465n I Environ. Sci. Technoi. 2012, 46, 7120-7127 US00005834 Environmental Science & Technology sFpiegcuirfeica1t.ioTnism. WelihnieleotfhAeFUFSFmpirloitdauryctuasedddiAtiFoFnFtositnhcee DtheepadretvmeleonptmoefnDteinfen19se63Q, uthaelifrieecdorPdrsodoufcAtsFFLFistoinngth(Qe UPLS)mtihliattarwyeQrePcLeratriefieodnltyo MIL-F-24385 available up to m19a7n6u.fAaclttuhroeurgFhir3eMSerrevmicaeinPeldus,onIntch.e QPL until 2010, the company ceased production of their AFFF product in 2002. "FSP" indicates the AFFF carbon chains with homologues of varying --CF2-- units.13 Although 3M voluntarily removed their AFFF products from manufacture due to the rising concern about PFOA/PFOS- based products in 2002,13,14 currently there is no restriction by the US government on the use of stockpiled 3M AFFF.14 However, both regulations to tcheaesEe uurosepeaonf Union and Canada have set forth and remove PFOS-based AFFF stockpiles.15,16 Other fluorochemical and AFFF manufacturers have agreed to comply with the EPA program to cease production of PaFllOCA8/P-bFaOseSd Stewardship fluorinated coBmoptohuMndSsDbSefaonrde 2015.17 patents pertaining to military list that these mixtures contain ftlhueoArinFaFtFeds used by the surfactants, although the exact elemental composition of these compounds ApiseFrfFplFuroosp.r1or8iaeltkFayorlry.suthTlfioshnearteesaisnsoganll,ets,aenaxsacleyinptidtciaioclnatteoidsolisnthaeMreSpDrneSeseefdnoecrde 3Mof to determine (e.g., reverse engineer) the composition of AFFFs sold to the military. Fast atom bombardment mass spectrom etry (FAB-MS) with unit mass resolution is an established qualitative technique that requires minimal sample preparation and that favorably ionizes hydrocarbon and fluorocarbon surfactants in commercial and environmental mixtures.8'19-21 As opposed to most LC-MS/MS methods, FAB-MS does not require prior knowledge of analytes of interest in order to analyze the samples (e.g., mass ranges, acidity/basicity, mixture composition, and concentration). In contrast, high resolution mass spectrometry (HRMS) with chromatographic separation allows for the accurate determination of ion masses, which can sibHadaeoemlanwpruteiglsfveeyesedrqco,oufttmaAhonepFtoFidmtuFyeantjfedooorsfrrmmodoinfubatelsiaantattiscetophlrneeaessctitiss.fpm2itc3ahu-na2snet5tilfneFbumgoleleransrrtctehaaadninlsugceHrceeoodRamfsMoimpnnSoa,nsopmiurtrifduooaevlnctritisdup.te2rloes2 ing years were first screened by FAB-MS to identify target analytes for further analysis by HRMS in order to determine the final elemental compositions of the fluorochemicals (Figure 2). Finally, the information on chemical structure was compared to structures given in patents. EXPERIMENTAL SECTION Materials. All solvents used for sample preparation and SanigamlyasisAbldyriFcAh B(-SMt.SLwouerise, HPLC-Grade quality or better from MO). Laboratory water at Oregon State University was deionized and cleaned with a Millipore Synergy UV Water System (Bedford, MA) that included a LC- Figure 2. Workflow scheme for the elucidation of fluorochemical surfactants in AFFF formulations. Pak C18 polisher. For FAB-MS analysis, MS-grade 3-nitro- benzyl alcohol (3-NBA) was purchased from Sigma Aldrich. UPLC/QTOF-MS analysis was performed at the Waters Corporation Facility in Pleasanton, CA. Solvents used for mobile phases and sample dilutions included Fisher Optima ALanCmdMmSoMngiilrulaimpdoearmceeetatMhteailnbliuo-flQffe,rrolwambasoFrmiasthaoderreySucswiienangttelirafibco((BrFaeatdoirfroyLrddaew,inoM,niNzAeJ)d). water and high purity ammonium acetate (Sigma Aldrich). NaSlgaemneplbeottCleosl)lepcutriochna.seSdamfropmle containers (60 mL HOPE VWR International (Radnor, PA) were shipped to 21 different US Navy and Air Force military bases within the United States. Sampling instructions also were sent that included sample handling and recording of pertinent AFFF formulation information. Sampling instructions specifically stated to sample AFFF from their original product container in order to avoid mixtures of products. Additional AFFF samples were sent by Bradley Williams of the US Naval Research Laboratory. In total, 74 QPL-listed AFFF samples were received with manufacturing dates ranging from 1984 to 2011. AFFF product names have changed over time; therefore, products were categorized by their manufacturer rather than product name and were reported as such ("3M AFFF", "Chemguard AFFF", "National Foam AFFF", etc.). After receipt, AFFF samples were stored in the dark at room temperature until analysis. MSFaasntalAysteosmwerBeopmebrfaorrdmmedenwtithMaasJsEOSLpeMctSro-RmOeUtrTyE. FABJMS- 600H magnetic sector mass spectrometer that was equipped with a FAB interface (JEOL, Ltd., Peabody, MA). Prior to 7121 dx.doi.org/10.1021/es301465nirnWron. Set Technal. 2012,46, 7120-7127 US00005835 Environmental Science & Technology Figure 3. Electrofluorination-based fluorinated surfactants identified in AFFF. The perfluoroalkyi chain lengths identified in AFFF are shown as the number of n fluorocarbons. The ionic species shown are estimated at an environmentally relevant pH. ganlyaclyoslism, itxhtuerein(swtriuthmeanvet rawgaes mcaolliebcrualtaerdwuesiignhgt aofp3o0ly0etgh/ymleonle) over keV, the m while /xzen1o0n0--g1a0s0w0a, sanudsetdheasiotnhizeaitoionnizaentieorngygaws.as set to 5 Each AFFF sample was diluted grade methanol, and an aliquot was amt ixleeadstw1it0h:13-wNiBthAHoPnLtChe- FAB probe. Samples were scanned over an m/z range from 100--1000 in both positive and negative ionization mode. A smmaaimnssipmlsepus,emctcrooafnw7siessrtcieanncgaslocwufelraoetnepdlyearsf3oa-rNnmBaevAde,rfaowgreeeroaefchtahlsesao7mapscnlaea,nlysa.zneBddlatnhtoke provide background mass spectra and to verify no compound carryover and/or contamination between AFFF samples. A number of AFFF samples from each AFFF manufacturer were analyzed in order to cover the entire range of available lot numbers and manufacturing dates. Multiple parameters were used to identify target masses for subsequent screening by high resolution Ions in a series characterized by spacings mofassms/pzec5t0ro, mwehtircyh. corresponds to --CF2-- units, were selected because they are ifnludoicriantaivtieono. fIofnlusorwoicthhemspicaaclisngsproodf umce/dz by electrochemical 100 correspond to --C2F4--units were selected because they can be characteristic of fluorochemicals produced by telomerization or electro- fluorination (Figures SI, S2).11,20 In addition, other masses that were identified in the FAB-MS spectra of multiple lots of the same AFFF were also added to the list of target masses. Ultra Performance Liquid Chromatography/Quadru- UpoPlLeC-T/QimTeOFo-fMFSli,ghatll Mass AFFF Spectrometry. For analysis formulations were prepared by in HPLC-grade methanol and diluted to ~12 ppb concentrations of fluorochemical surfactants as estimated from information provided by the available MSDS. Blank samples (consisting of 50% 0.5 mM ammonium acetate in water and 50% methanol) were injected regularly throughout the sequence to verify that there was neither system contamination nor analyte carryover. Separations were performed on a Waters Acquity H-Class UPLC (Waters Corp., Milford, MA); the chromatographic conditions are reported in the Supporting Information (SI). The chromatographic conditions selected provided the minimum resolution interest. A Waters XreeqvuoireGd 2to separate the suspect ions of Quadrupole-Time of Flight (QTOF) mass spectrometer with electrospray ionization (ESI) was operated as the high resolution mass spectrometer. Voltages for the cone and capillary were 30 V and 1.50 kV, respectively. Additional parameters included a source temper ature of gas flow 130 C, a of 25 L/h, desolvation temperature of and a desolvation gas flow o f3510000CL, /ah.coMnSe scan time was 0.1 s with an MS scan range of 150--1000 m/z. Every 15 s, the system was recalibrated using leucine- enkelphalin as the lockmass, and the resolution was set to be 20,000 (unitless, defined as the peak width at half-maximum). All samples were analyzed in both positive and negative ionization modes. UPLC/QTOF chromatograms for each of the AFFF formulations were first screened for only compounds that had mass defects from --0.100 to +0.150, which is typical of fluorochemicals. Mass defects are the difference between the actual/theoretical ion mass from the nominal ion mass. For ieoxnammp/lez:5P0F0.O00S0h0a, sfoarnaamctuasasl ion m defect /z o 499.9375 and a nominal f m /z --0.0625. The low- to-negative cumulative mass defects negative mass of fluorochemicals are due to defect of multiple fluorine atoms (tmhe/ z --0.0016) and can be compared to the positive mass defect created by multiple hydrogen atoms (m /z +0.0079). Chromatograms were extracted for each target mass. High accuracy masses (to the ten-thousandth of a mass-to-charge unit) were calculated as an average over the entire peak width, which has been reported to give the most reproducible results (Figures S3, S4). 6 Possible elemental compositions of the high-accuracy masses were calculated along with the error, which is reported as the deviation of the detected mass from the calculated elemental composition's mass (in parts-per- 7122 'fccdoi.org/l0.102l/es301465n I Environ. Sd. TedmaL 2012, 46, 7120-7127 US00005836 Environmental Science & Technology n =F4 ,6 ,8',-1--0----S------NH F `I 11 = 6,8 ri B O. H nt F-ji 8 \ n = 6,8 ,NH* Figure 4. Telomerization-based fluorinated surfactants identified in AFFF. The perfluoroalkyl chain lengths identified in AFFF are shown as the number of n fluorocarbons. The ionic species shown are estimated at an environmentally relevant pH. million [ppm]). In addition, the elemental composition of the +1 and +2 isotopes were used to rank the likely parent 7soetl;freascmuianelrftnbsuotrain:nl:c0l0--cu--od7m;5e0paa;nonhdsiyetfrdiloruronoorsgr.ielninmeT::iht00e--o--f52e05l;e.5moxpeypngmteanl:an0cdo--me7l;pemonsietirtniotoagnel nli:cmo0int--s PaPteanttesntreIlnaftoedrmtaotioAnFFanFd foSrtmruucltautrioensCocnofnirtmaiantiolinm. itUedS information on the functional groups and possible perfluor oalkyl chain lengths of fluorochemical components. A database was compiled, which contained the masses and elemental formulas for all potential AFFF fluorochemicals identified in pQaTteOntFs. The high accuracy masses detected by analysis and their calculated elemental the UPLC/ composition wfroerme then matched to those patents to confirm the in the final structural structures database derived of the identified fluorochemical compounds. RESULTS AND DISCUSSION Electrochemical Fluorination-Based AFFF. 3M AFFF. From the sampling program, 19 samples of 3M AFFF were received from US Air Force and Navy bases within the United S1t9a8t8est.oT2h0e01s.amAlpthleosuhgahd3aMrAanFgFeFosfwmeraenupflaaccteudrionng dates from the QPL in 1976, attempts to locate samples older than 1988 were unsuccessful. Six representative 3M AFFF samples were qualitatively analyzed by FAB-MS. The FAB-MS ionization mode spectra of contained 3M AFFF spadngs o fobmta/inz ed50i,n negative which is characteristic of fluorination.20 compounds In the 3M syAnFthFeFs,izeCd6f--roCm8 electrochemical perfluoroalkyl sulfonates (Figure 3A) were identified components in all the 3M AFFF tested (Table Si), and this is consistent with the frequent detection of perfluoroalkyl sulfonates found in AFFF- impacted groundwater.4'5'7'8'27 Contrary to these findings, however, no perfluoroalkyl carboxylates were detected in any AFFF product, with dates that ranged from 1988 to 2001. However, PFCAs are reported as primary components in early 3M AFFFs.11 A limitation of the FAB-MS/QTOF-MS method is that it can only capture the major components and that minor (approximately <0.1%) fluorochemical compounds may go undetected; therefore, if PFCAs were an impurity and/or minor component of the analyzed AFFF products they could not be detected with the current method. Current research udesitnergmLiCne/Md SPMFCSAtso determine trace components in AFFF has are present in some 3M AFFF (unpub lished work), While chemical degradation could occur during long-term storage of any AFFF product, it was beyond the scope of the study to determine the stability of fluorochemicals in commercial AFFF mixtures during long-term (e.g., decades) storage. In addition, 3M AFFF were comprised of zwitterionic C4-- C6 perfluoroalkyl sulfonamides containing carboxylic add and tertiary amine functionalities (Figure 3B), which are consistent with patent information28 and Material Safety Data Sheets (MSDS) that list "amphoteric fluoroalkylamide derivatives".29 The identification of these compounds was made in positive ionization mode, an uncommon method of mass spectrometric 7123 dx.doi.org/10.1021/esBOl465n I Environ. Set. Technol. 2012, 46, 7120-7127 US00005837 Environmental Science & Technology AaidonaFnatFiilnzyFagzsteid1om9,na8nt8fhouerofarfczlt1uwu9ori8tre9tode.crihTinoehnm1ei9cic39aM3cl,odm1Ae9Fpt9eFo8cuF,tinsaodnnwsd.e2Orwe0ef0rr1teehcbeefruotstiuifxnnieod3dtMiionnnAtl1yhF9o9Fsi2Fne, but not thweelaldddioticounmoefnztwedit.t3e0r'3i1onAicFfFluForofocrhmemuliacatilosntor3eMcerAtiFficFaFtisoins would occur if there were changes to military specifications or if the AFFF formulation itself was significantly changed (i.e,, a change in chemical components). An additional set of ions of lower abundance was observed in positive ionization FAB-MS wticnhhidatehtimcamcictoeaarlsrCseces5lspa--sotshCnad6sthewdopweertrnoefluitnohrmeoFai/zlgzkwuy7rilte2tes3durBiiloff.foneniTrcaehmnsetuid(lafTedoandcbaiotlmiemoinSpdoeio)ufncflrdmaossm/szwbti7huth2et an additional propanoic add branch (Figure 3C), and the loss of m /z 72 indicates the absence of the propanoic add branch (Figure 3D). These derivatives are impurities from the synthesis as indicated in the AFFF patent.28 No C8-based homologues of the zwitterionic corresponding impurities (Figure 3Ccla-Dss) (Figure 3B) or were identified. the Telomerization-Based AFFF. National Foam AFFF. Nineteen samples were collected from military bases with manufacturing dates ranging from 2003 to 2008. Although National Foam has AFFFs on no samples from 1976 to 2003 the QPL since were acquired. S1ix97r6ep(rFeisgeunrtaetilv)e, samples were analyzed by FAB-MS. The primary fluorochemicals of National Foam AFFF were detected by m/z 100 spacings in both positive and negative mode FAB-MS, which correspond to --C2F4-- units that are characteristic of telomer-based fluorochemicals. The targeted ions were then identified by QTOF-MS as the 4:2, 6:2, 8:2, and 10:2 fluorotelomer sulfonamide with dimethyl quaternary amine and carboxylic add functional groups (Figure 4A; Table S i).32 Less abundant ions were identified with m /z --58 differences from the 4:2 and 6:2 fluorotelomer ions, which are related to the same structure but without the terminal acetic add functionality (Figure 4B). In the related patent, Norman et al. suggest that these compounds could result as a byproduct in the synthesis of the major betaine compound.32 Ansul AFFF. Ansul AFFF, along with 3M and National sFFaoimfatempel,ninwgsaapsmroppgllraeascmed,o fwoinAthntsmhueal nAuAfFFaFFcFtFuriQwnPgeLrdeaitnceos l1tlhe9c7at6tedra(Fnfgirgeoudmrefrotlhm)e. 1984 to 2010 (Figure l), of these eight representative samples were analyzed by FAB-MS. Negative ionization mode FAB-MS analyses for Ansul AFFF revealed two abundant ions with characteristic fluorotelomer mass spacings of m /z 100 (Table S i). The primary components identified in the Ansul AFFF were the 6:2 and 8:2 fluorotelomer thioether amido sulfonates at m /z 586 and 686, respectively (Figure 4C). This structure is supported by multiple patents33-33 and a limited number of other reports on AFFF composition.8'20 An ion of lower abundance was identified at m /z 602, corresponding to a mass difference of m/z 15.9940 from the 6:2 thioether amido sulfonate and is proposed to be the addition of an oxygen atom (structure not shown). The identity of this fluorochemical class could not be definitively determined from the mass spectral data nor from the patents and may be a synthetic impurity. The 6:2 fluorotelomer sulfonate was also reported as being detected by no LfluCo/rMotSe/lMomSerinsuAlfnosnualtAesFF(FFT,8Sb) uwt ewreithdettheectceudr. rTenhtemlaectkhoodf identification of FTS in AFFF formulations is most likely due to the aforementioned high detection limits, and current work developing a quantitative LC-MS/MS method will determine these trace components. Angus AFFF. Only one sample of Angus AFFF was received and analyzed. Because there was no recertification from the time that the product met Mil-Spec in 1994 to present (Figure l),30'31 and there were no formulation changes that necessitate recertification, the single sample may well represent the entirety of Angus AFFFs regardless of the year of manufacture. In the Angus AFFF formulation, the 6:2 fluorotelomer thioether amido sulfonate (Figure 4C) and corresponding oadxydgiteionna,tedtwiompmuaristsyes(startucmtu/rze not 496 sahnodwn5)96wewreerdeetiedcetnetdi.fieInd through analysis, positive ionization the structure was FAB-MS analysis. determined to be Ba y6:Q2TaOnFd-M8:S2 fluorotelomer thioether with hydroxyl and trimethyl quaternary amine functionalities (Figure 4D; Table Si).33 Chemguard AFFF. From the sampling program, 11 samples were received from US military bases, and the manufacturing dates ranged from 2006 to 2010. While this is a narrow range of dates, there htahveerebweeans no no AFFF sample recertification, and therefore official formulation changes.30'31 Therefore these samples are likely to be representative of the QPL-listed AFFF product. Five representative samples were analyzed by FAB-MS. Within the samples analyzed by FAB-MS, there were distinct differences between Chemguard products with manufacturing dates from 2006 to 2007 and 2008--2010. The FAB-MS spectra of the later manufacturing years had no patterns characteristic of fluorochemicals detected through positive and negative ionization FAB-MS, but there was a single strong peak detected at m /z 586, which was previously identified as the 6:2 fluorotelomer thioether amido sulfonate (Figure 4C) and verified by QTOF-MS. The other homologues of the fluorotelomer thioether amido sulfonate (4:2, 8:2, 10:2) may be present at concentrations below the above-specified detection limit. In the earlier manufacturing years, fluorochem ical was patterning identified was by identified for QTOF-MS mto/zb6e02t,h7e02s,oadniudm8-0a2d,dwuhctiechd compounds of compounds with m /z 581, 681, and 781. These compounds were identified as 6:2, 8:2, and 10:2 fluorotelomer thioether amido amino carboxylic add (Figure 4E; Table S i).36 Buckeye AFFF. Buckeye AFFF was initially certified for military use in 2004, making it the second most recent product to be added to the QPL (Figure l).30,31 Only one sample of QPL-listed Buckeye AFFF was received from a military base, and an additional sample was supplied by the US Naval Research Laboratory; both of these samples were analyzed by FAB-MS. No characteristic mass spadngs of fluorochemicals were identified by analysis under negative ionization FAB-MS. Two dspifafceirnegn)t series of fluorotelomer-based homologues (m/z were detected in positive ionization mode at m /z 100 432, 532, and 632 and m /z 414, 514, and 614 (Table Si). Based on AFFF patent information,33 the fluorochemicals were identified as fluorotelomer betaines with quaternary amine and carboxylic acid functionalities (Figure 4F and 4G). The difference between the two series of homologues is 18 mass units, which is identified as the substation of a hydrogen atom with a fluorine atom near the fluorotelomer chain. Both compounds have perfluoroalkyl chains with lengths of 5, 7, and 9. The compounds with the additional fluorotelomer chains are referred tfoluoarsinxe:y:aztofmluornoetaerlomtheer 7124 dx.doi.oig/10.7021/es301465n I Environ. S cl Technol. 2012, 46, 7120-7127 US00005838 Environmental Science & Technology ______________ fnbloeutnoafrilniuneoart(ieFndiagtuecdraerbc4oaFnr)bs,,oinnysdicpsaritniiongrlgyttohfaluttohtrehienafictroesdmt pfcuoanurcnbtdioonnhsaa,sl x fully and z group (quaternary amine) (Table Si). These compounds do not follow chain the typical lengths.11 telomerization In addition, pattern of even the structure offluotrhoecaxrb:yo:nz fluorotelomer betaine does not follow the typical telomerization paradigm of a fully fluorinated carbon chain (with the singly fslturuorcitnuaretedrescualrtsbofnromlinkthagee)u.seThoef synthesis of this unique an unsaturated fluoroalkyl amine.37'38 waserFtehireereASceeFirFvveFicdejforPionlmuesdtAhthFeFesFam.mNilpiotlainrFygirpQerPoSgeLrravimince,2wP01hlu1ics.hAHwFoaFwsFeevsxeaprm,ecpttwleedos Fire Service Plus samples (from the same manufacturing batch) were received from the Naval Research Laboratory and analyzed. Positive ionization mode FAB-MS analysis of Fire Service Plus AFFF showed fluorotelomer characteristic spacings (m/z 100) at the same masses as the National Foam AFFF. This was vpeerrfifliueodroaaslktyhl echfaluinorloetneglothmseor f sulfonamide 4, 6, 8, and betaine class with 10 (Figure 4A). In addition, the 4:2 and 6:2 fluorotelomer sulfonamide amine impurities were also identified in the formulation (Figure 4B). As the newest addition to the AFFF QPL for US military use, it is very unlikely that there has been any environmental exposure of this AFFF due to uncontrolled or controlled releases of the material. Environmental Implications and Research Needs. This ipsoloynfeluoorfinthateedfirsstursftaucdtaienststocorenptaoirntetdheinidemnitliittiaersy-oufseperA-FaFnFd. While the specific compounds are now known, the environ mental behavior and toxicity of the individual fluorinated surfactants (and as mixtures) are still unknown. Previous studies have examined the presence of PFOS and the other perfluoroalkyl sulfonic acids in environmental samples due to AFFF-use and have detected relatively high concen trations of these compounds in groundwater.5'7'8 While Schultz et al. reported the identity of the fluorotelomer thioamido sulfonate in AFFF formulations, no data occurrence were obtained.8 Oakes et al. aolnsoitisncelnuvdierdontmheen6ta:2l and 8:2 although fnluoovraoltueelos mfoerrencovmiropnomunedntsalinprtehseeinrcaenwaelyrteicraelpmoretethdo.3d9 The scope of the current study was to qualitatively identify the vflauroioruocsheMmSicDaSl components to range in in AFFF, which concentrations of 0a.r5e--2li5s%ted in (by weight) in the product concentrate. On-going research is underway to develop LC-MS/MS methods with the capability for quantifying trace levels all of the newly identified fluorochemicals in groundwater, sediment, and soil. Such methodology can be applied to future studies on the fate of tshysetenmews layniddetnotiefvieadlufaluteorthocehiremociccualrsreinncneaatunrdalefafnecdtseninginbieoetrae.d Of the 11 fluorinated surfactant classes reported in this study, 9 were determined to have cationic or zwitterionic function alities at environmental conditions (Figure 3B-D, Figure 4A, B, D-G). The nature of these fluorinated surfactants in the environment has not been investigated in the peer-reviewed literature. Cationic (nonfluorinated) surfactants have different environmental transport characteristics than anionic surfactants. For instance Lee et al. reported that the studied cationic surfactants would cation-exchange onto the negatively charged surfaces of sediments and therefore retard the transport of the _________________________________________________________ compounds through the environmental system.40 In addition, the adsorbed cationic surfactants could act as a carbon loading surface that further retained other hydrocarbon compounds at the source fluorinated of contamination.40 Cationic surfactants may also behave in aansidmilzawritmtearnionneirc, suggesting that groundwater sampling may not be sufficient in the detection of these compounds in the environment. Fausrinthketromroertea,inthfeluocaroticohneimc ifclualosroocraortbhoenr surfactants may act as priority pollutants and create long-term source zones of high fluorocarbon contami nation. Most of the studies perfluoroalkyl carboxylic also adds f(oPuFnCdAsd) etienctAabFlFeF-liemveplascteodf PgcorFonCutaAnidsnwemdaatPyeFrh,C5a-vA8es'2b7ae's3e9an'4m1maajbjoourrtccoonmmopnpoeonneeonnftt.sAthosefp3rMaenvAiaolFuyFzsleFydpalrAliuoFdrFetdFo, 1988 or are minor (e.g., < 0.1%) components of current AFFF at trace levels. In addition, the presence of PFCAs may be due to the degradation of other fluorochemicals. Wang et al. reported the degradation of fluorotelomers to the correspond isnlugdcgaer.4b2oxWyloarteks through aerobic biotransformation in activated by Houtz and Sedlak has shown, through the advanced oxidation process, that more functionalized fluo rocarbon surfactants can be degraded down to the more oxidation-resistant fluorinated carbon backbone, resulting in the production of corresponding perfluoroalkyl carboxylates.43 This has important implications toward the application of in situ chemical oxidation (ISCO) remediation processes that may be used to dean up contaminated sites that may also contain these AFFF-based fluorochemicals. These examples suggest that not only do the AFFF compounds present their own environmental and toxiocological concerns, they also could be potential sources of perfluoroalkyl carboxylates through environmental and anthropogenic transformation. Future research studying the fate of the fluorochemicals during biodegradation and upon exposure to chemical remediation approaches (e.g., ISCO) is needed. The data from these experiments will have important ramifications btoawseasr.dTthhee site closure of fluorochemical-contaminated military targeted approach based on FAB-MS described in this study may be useful in the identification of transformation products of the fluorochemicals identified in this study if they continue to exhibit surface-active properties. However, FAB- MS analysis has poor sensitivity (approximately mg/L levels) compared to that of LC-MS/MS (ng/L), which is necessary to dcoemtecbtinterdacwe iltehveQlsToOfFinatenramlyesdesiatmesa. yTbheeremfoorree, LC-MS/MS suitable for environmental transformation and/or bioaccumulation studies. In addition to understanding the environmental behavior of these fluorochemicals, it is mportant to understand the implications of remedial strategies applied in the field. For example, `pump and treat' access the positively charged rfelumoerdoicahteiomnicmalsaythnatotcobueld acbalteiotno exchange to the sediments. In addition, advanced oxidation could potentially result in the increase of `dead end products' (such as the perfluorinated carboxylates), some of which are compounds of concern. Development of new approaches to fluorochemical remediation may be important to fully account for the various classes identified in this research. bagaArseeseddpArtFeovFitFohueisnlvy2o0nlu0on2tet,adwr,yh3irlMeegtuhcleeaatrsieoesdntspoorfofthdtuehceAtiFEoFnPFAomfPtaFhnOeuirAfa/cPPtFuFOrOeSrSs- Stewardship Program, which calls for the complete phase-out of 7125 dx.doi.org/10.1021/es301465n I Environ. Scl. Technol. 2012, 46, 7120-7127 US00005839 Environmental Science & Technology C8-based products from materials. As reported in this study, while most AFFF formulations did contain C8 and above AmfflluuFoooFsrrtFoinciwnahtteeeermdnesiscoeuafrlspfiaghecrnotfamalulnootvslrio,oagtahuFlkeeAysmlBoc-aMhfjoacSrihn)ahliioennnmgltoethnhleogsgttluheeelsos8m(tiohderaerinngztrai8eft,iiaeoatdneltr-habowsaustegehrhdee itrdheeseenatri2fc0ihe1d5coautdledleasdbsleeirnaeip,npteltionesditviteeosri.ffuyTtuhtreheemAeFrtFehmFodofvodarlemscuorlfaibtieCodn8s-i,nbaatsfhteeidsr fluorochemicals from these products, ASSOCIATED CONTENT O Supporting Information Materials and methods, Figures S I --S4, and Tables SI and S2. This material is available free of charge via the Internet at http://pubs.acs.org. AUTHOR INFORMATION CedouPr.hreonsCepo:ornr5ed4si1pn-og7n3dA7i-un2tg2h6o5ar.uthEo-rmaaild:drJeesnsn: ife1r0,F07ieldA(LSoreBgounilsdtiantge,. Oregon State University, Corvallis, OR 97331. Notes The authors declare no competing financial interest. ACKNOWLEDGMENTS The authors would like to acknowledge Mike Wakefield and Greg Witkop of the Waters Corporation for their assistance with UPLC/QTOF-MS and data analysis. We would like to acknowledge Bradley Williams of the U.S. Naval Research Laboratory, Donald Warner of the U.S. Air Force, and all of the participating U.S. Navy and Air Force bases for the collection and shipment of the AFFF materials. In addition, we thank the Fire Fighting Foam Coalition, especially Executive Director Tom Cortina, for their technical assistance and historical knowledge on the use of AFFF. This study was supported by Oregon State University's Department of Chemistry N.L Tartar Fellowship and the Strategic Environmental Research and Defense Program (SERDP) grant number ER-2128. 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