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AR226-2363 9 ------ "| Hl i| Detecting and I Quantifying | Low Levels of Lo Fluoropolymer i Polymerization Aids -- 2 A Guidance Document I | Cl| bl | )y i . i FESLySae IEr eE "Technical naVeeGroup (AWG) This page left intentionally blank. EXP000572 NOTE TO USERS This Guidance Document was developed by die Fluoropolymer Manufacturers Group of The Society of die Plastics Industry, Inc. and is intended to provide information on general guidelines for die determination of fluoropolymer polymerization aids in a variety of matrices. The guidelines provided are based on die collective experience of members of me industry, but are not intended to be either exhaustive or inclusive of all pertinent requirements. The information provided in mis guide is offered in good faith and believed to be reliable, but is made WITHOUT WARRANTY, EXPRESSED OR IMPLIED, AS TO THE MERCHANTABIUTY, FITNESS FOR A PARTICULAR USE, OR ANY OTHER MATTER. The guidelines provided and me examples included are not intended to be directed to any particular product, nor are they claimed to satisfy all current requirements of Good Laboratory Practices. Following me Guidance Document does not guarantee compliance with any regulation or standard, safe handling, nor safe operation of laboratory equipment Users are cautioned mat the information upon which mis Guidance Document is based is subjectto change, which may invalidate any or all of me comments contained herein. This Guidance Document is not intended to provide specific advice, legal or otherwise, on particular products or processes. In designing experiments and operating equipment, users of this Guidance Document should consult with their own legal and technical advisors, their suppliers, and other appropriate sources (including but not limned to product or package labels, technical bulletins, or sales literature) which contain information about known and reasonably foreseeable health and safety risks of their proprietary products and processes. SPI, its members and contributors, do not assume any responsibility for the user's compliance with any applicable laws and regulations, nor for any persons relying on the information contained in this Guidance Document SPI does not endorse the proprietary products or processes of any manufacturer or user of fluoropolymer polymerization aids, resins or products, or any manufacturer or user of laboratory instruments or supplies. All information about an individual manufacturer's 'products contained herein has been provided by those manufacturers who are solely responsible for me accuracy and completeness of me data. Copyright 2003 The Society of the Plastics Industry, Inc. All Rights Reserved SPI Literature Catalogue #: BZ-102 -A Determining Low Levels of Fluoropotymer Polymerization Aids Guidance Document Copyright 2003 The Society of the Plastics Industry. Inc., All Rights Reserved EXP000573 This page left intentionally blank. EXP000574 Determining Low Levels ofFlnoropolymer Polymerization Aids A Guidance Document 1.0 Purpose.................................................................................................. I 2.0 Introduction............................................................................................ 1 3.0 Safe Handling Information......................................................................... 3 4.0 Analytical Technologies.............................................................................. 4 5.0 Analysis ofPFOA in Water......................................................................... 5 6.0 Analysis ofAmmoaipm Perflnorooctanoate (APFO) m Air................................. 7 7.0 Determination ofAmmoninm Perflnorooctanoate (APFO) m Biological Matrices.... 8 8.0 Solids.................................................................................................... 9 9.0 Additional Ana^tical Considerations............................................................ 9 10.0 References.............................................................................................. 11 b TABLE 1: General Terminology and Definitions.................................................... 2 TABLE 2: Definitions of Quality Assurance (QA) Criteria........................................ 10 TABLE 3: Physical and Chemical Properties......................................................... 14 APPENDIX A: Examples ofFlnoropolymer Polymerization Aids................................ 12 APPENDIX B. General Physical and Chemical Properties......................................... 13 APPENDIX C: Comparison of Available Analytical Techniques for Ftuoropolymers........ 16 EXP000575 This page left intentionally blank. EXP000576 1.0 Purpose This document will focus on die determination of low levels of Fluoropolymer Polymerization Aids (FPAs) in various matrices. This document is not meant to be all-inclusive, but rather to emphasize the state of knowledge and the difficulty of ensuring reliable sampling and data acquisition on these materials. Since the FPAs cover a wide range of chemical structures, a successful method for one compound does not necessarily ensure the method will be as useful for another. Also, this document will direct the reader to a subset of the appropriate literature that will be useful in establishing analytical protocols. Table 1 will provide the reader with the terminology and definitions used in the field. 2.0 Introduction Fluoropolymer Polymerization Aids (FPAs) are used in diverse industrial applications as surfactants, dispersants, etc. The most common use of FPAs is as surfactants. Fluorosurfactants are similar in structure to conventional surfactants in that they have a hydrophilic part and a hydrophobic part. The difference lies in that the hydrophobic part of the fluorosurfactant molecule contains fluoridated carbons. The extent of the fluorination and the position of the fluorine atoms in the surfactant molecule affect die characteristics of die fluorosurfactant Consequenfly, die surfactants may be termed either partially or fully fluorinated (aka perfluorinated). The hydrophobes of partially fluorinated surfactants contain bodi fluorine and hydrogen atoms. Unlike die hydrophobes of hydrocarbon surfactants, die partially fluorinated hydrophobe consists of two mutually phobic parts which are not compatible. Consequendy, partially fluorinated surfactants exhibit anomalies in macroscopic characteristics, such as critical micelle concentration (cmc), and in microscopic phenomena as well. However, partially fluorinated surfactants have several advantages over fully perfluorinated surfactants. The hydrocarbon segment provides solubility in more commonly used solvents, lowers die melting point of me surfactant, reduces volatility, and decreases die acid strengdi of fluorinated acids.1 Perfluorinated surfactants are remarkably stable, having exceptional diennal and chemical stability, which enables them to be used in applications diat would be too severe for conventional hydrocarbon-based surfactants. The very strong C-F bond in a carbon chain (note: die F attached to C=0 is not stable) is stable to acids, alkali, oxidation, and reduction, even at relatively high temperatures. It is dlis very stability diat is die root cause of die difficulties in die determination of low levels of FPAs using conventional analytical techniques. Fluorosurfactants as a class of compounds cover a range of chemical structures. Like all surfactants, fluorosurfactants are eidier ionic or nonionic. Ionic surfactants can, unlike nonionic surfactants, dissociate into ions in an aqueous medium. The hydrophilic part can belong to a negative or positive ion. Fluorosurfactants can be classified into four types: 1) anionic, where the hydrophilic part is an anion; 2) cationic, where die hydrophilic part is a cation; 3) amphoteric, which have at least one anionic and one cationic group, and 4) nonionic. Like dieir hydrocarbon counterparts, ionic fluorosurfactants dissociate in water and form a surface-active ion widi an oppositely charged counterion. It is die surface-active ions of anionic fluorosurfactants diat bear die negative charge. It is die anionic fluorosurfactants diat are die most important class of fluorinated surfactants. They are classified based on the structure of EXP000577 Table 1. General Terminology and Definitions Fluorinated Chemical Fluorinated Organic Polymer Fluorinated Organic Surfactant Fluorochemical Fluoropolymer Fluoropolymer Polymerization AFluiodr_os_u_ria_c_ta_n_t Perfluoro- / Perfluorinated Perfluorinated Surfactant Perfluoroalkylated Substance A general, non-specific term used synonymously with "fluorochemical." A general tenn used to describe a polymer which has a hydrocarbon backbone (polyamide, polyester, polyurethane, etc.) to which is appended a fluorinated carbon chain, also known as a fluorinated alkyi chain; an example would be a polymer such as -[CH2CH(C(0)OCH2CH2(CF2)gF)3, A term to describe a surface active, low molecular weight (<1000), substance which contains fluorinated carbons; the term fluorosuriactant is non-specific but often used synonymously; an example is F(CF2)(,CH2CH2S03"NH4+ _ _ A general, non-specific term used to describe broadly all chemicals containing the element fluorine; specifically, the term is used most commonly to describe small (1-8 carbon length) fluorinated molecules that are most often used for re&igeradon, as fire suppression agents and as specialty solvents. A general tenn used to describe a polymer which has fluorine attached to the majority of carbon atoms which comprise the polymer chain backbone [common fluoropolymers are: polytetiafluoroethylene (PTFE), polyvinylidene fluoride (PVDF), fluorinated ethylene-propylene (PEP), etc.]; these are typically high molecular weight polymers used in high performance applications where chemical resistance and thermal stability are essential. A general term used to describe a subset ofperfluoroalfcylated substances; members of a class of commercially available perfluoroalkyi carboxylate surfactants, dispersants, etc. A non-specific, general term used to describe a surface active, low molecular weight (<1000), substance where carbons bear fluorine in place of hydrogen. Examples would include CF3(CF2)7S03'K+, H(CF2)7COO" NH4+, F(CF2CF2)3CH2CH2S03NH4+,CH3CH2CF2CF2CH2COO-NH4+, etc. Describes specifically a substance where all hydrogen atoms attached to carbon atoms are replaced with fluorine atoms - CFn - where n = 1 - 4. A term used to describe a surface active, low molecular weight (<1000), substance where all carbons bear fluorine in place of hydrogen; the tenn fluorosurfactant is less specific but used synonymously; an example is F(CF2)6S03'NH4" A general term describing a substance that bears a perfluorocarbon unit, also known as a perfluroroalkyi functional group, F(CF2)n-R, where n is an integer and R is not a halogen, or hydrogen. Examples include F(CF2)6CH2CHzOH, F(CF2)6SC>2N(CH3)CH2CH20H, and p-F(CF2)6- C^OH EXP000578 ifaeir hydrophile, which can be divided into four main categories: a) carboxylates (R^OO'M4), b) svlfooates (RiSOsM"), c) sutfates (RiOSOs'M1), and d) phosphates (RfOP(0)02"M24), where Rf is a fluorine-containing hydrophobe and M^ an inorganic or an organic cation- The predominate fonn used and for which there is the most analytical data are the perfluorinated carboxylic adds (PFOAs) and their salts. In cationic fluodnated surfactants, the fluorinated hydrophobe is attached directly or indirectly to a protonated ammo group, a quaternary ammonium group, or a heterocyclic base.1 Canonic surfactants dissociate in water, forming a surface-active positively charged ion and a negatively charged counterfoil. Like anionic surfactants, cationic surfactants are usually affected by the pH of the medium and the electrolytes. There is a general belief that cationic surfactants adsorb on negatively charged surfaces.1 Amphoteric fluonnated surfactants are bifunctional compounds having at least one cationic group, one anionic group, and are electronically neutral around their isoelectric points. Amphoteric fluonnated surfactants can function both as anionic and as cationic surfactants depending on the pH of the medium.2 They are compatible with other types of surfactants and are believed to absorb on either positively c negatively charged surfaces.1 Amphoteric fluonnated surfactants are used in foam stabilizers, emulsifiers for manufacturing fluoropolymers, wetting agents, repellants for paper and textiles, fire-eExtinguishing agents, spreading agents on hydrocarbon surfaces, cleaning agents for degreasing metal surfaces, and personal care products. Nonionic fluorinated surfactants are soluble in an acid or an alkaline medium. They do not dissociate into ions in water. Consequently, nonionic fluorinated surfactants are less sensitive to pH and electrolyte changes. They are not preferentially adsorbed on charged surfaces.! Appendix A covers some of the structure types of these molecules. Appendix B discusses general physical and chemical properties. 3.0 Safe Handling Information for Fluoropolymer Polymerization Aids Read safety information prior to use, including MSDSs, and the Society of the Plastics Industry, Inc. (SPI) "Guide to Safe Handling of Fluoropolymers Dispersions," available either online (http://www.iluoropolymers.org/news/APFOsafebandlmgguide.pdf) or directly from SPI.3 Any information, whether in an MSDS or in this guide, may change as results of further studies become available. Consult your supplier or SPI for the most up-to-date information. A general treatment of physical and other properties of FPAs may be found in Fluorinated Surfactants.1 The majority of the toxicology data and health studies on FPAs have been conducted on ammonium perfluorooctanoate (APFO). APFO is a perfluorinated chemical; it is extremely stable, degrades slowly, and therefore persists in the environment. APFO can be absorbed by the body and may be detected in the blood stream following ingestion, inhalation or skin contact APFO has been classified by the American Conference of Governmental Industrial Hygienists (ACGffl) as an animal carcinogen, but available evidence does not suggest that the agent is likely to cause cancer in humans except under uncommon or unlikely routes or levels of exposure.4 Use of engineering controls, good hygienic practices and personal protection equipment (PPE) are critical in reducing exposure to FPAs. Avoid contact when handling materials containing FPAs. FPAs may be released when dispersions are heated or dried. Although solids, <!<%>. EXP000579 some FPAs have high vapor pressures. It is important to clean up spills before they dry and allow the FPA to sublime. Handle all chemicals with caution, including <fluorosurfectants. It is the responsibility of the individuals handling neat materials, standards, and samples to determine the most appropriate precautions to follow based on available information. 4.0 Analytical Technologies The logical approach to determining which analytical method to use for a particular application is to define the need, determine which analytical technologies might be able to solve the problem, determine if these resources are available in a timely fashion, and if so, proceed. Often the process is not as simple as it might seem, especially if the analyte of interest is difficult A useful tool to define the need is "Fitness for Purpose." Fitness for Purpose is the property of data produced by measurement mat enables the user of the data to make technically correct decisions for a stated purpose.5 Fitness for Purpose refers to the magnitude of the uncertainty associated with the measurement in relation to the needs of the application area. For many applications ofperfluorinated fluoropolymer polymerization aids, it might be sufficient to simply determine the total fluoride after combustion witfa a fluorine ion-selective electrode. For measurements required in an industrial, regulated environment, it would be necessary to have more exacting quantitative and qualitative tools with defensible quality assurance as an integral part of each step. The following checklist might also be a useful tool in selecting the analytical method. What is me purpose of the measurement? What concentration of analyte is expected? How will the material be identified? What quality assurance procedures are required? How will sampling and transport be accomplished? What are the sources of potential cross contamination? What is the method specificity? Should screening be used to expedite the measurement process? What is the linearity and range of the measurement? What is the detection limit (both method and instrument)? What is the stability of me sample in the containers and conditions from sampling to analysis? What type of error analysis is appropriate? What criteria are needed to reject data? (R2, blank less than the method detection limit (MDL), nonzero blanks) Validation Time, money, resources Have you carefully considered the next steps ("What if' planning) after the data are obtained? In evaluating the overall Fitness for Purpose, consideration should be given to the resources needed to improve the accuracy, precision, and qualitative nature of the analysis. Generally, the more precise, accurate, and certain, the higher the cost and greater the time needed. 4 EXP000580 The most common fluoropolymer polymerization aid is ammonium perfluorooctanoate, APFO. Since it is the most common material in use, it is also the most studied and reported upon. In water, APFO dissociates into its anion, perfluorooctanoate, and its cation, ammonium. For analytical measurements, the concentrations are usually expressed as the original ammonium salt (APFO) or its parent, perfluorooctanoic acid (PFOA). The following sections will highlight various aspects involved in me sampling, sample preparation, analysis, and data reduction for PFOA. 5.0 Analysis of PFOA in Water 5.1 Sampling and Preservation Care must be used in sampling to avoid later problems in analysis, especially when determining perfluorooctanoic acid (PFOA) and its salts at part per billion (ppb) levels or less. It is important mat multiple blanks and standards are run. If blanks show measurable quantities of PFOA, results should be considered suspect To avoid contamination from sampling equipment and containers, fluoropotymers should be avoided, since PFOA is often used in fluoropolymer manufacture. Field blanks can help to identify problems in this area. It is important to ensure the sampling equipment being used is not subject to adsorption, absorption, or volatilization losses, and does not compromise me sample. Sample history should be well documented and contain details of sample collection and transport. It is important to verify hold times for analyses of this type. If not analyzed promptly, samples should be stored at temperatures at or near zero degrees Celsius. 5.2 Preparation Different types of water have different sample preparation issues associated with them. If the PFOA salts dissolve more readily than me free acid, it may be necessary to adjust solution conditions through the addition of appropriate bases, such as ammonium hydroxide (see Appendix B). Since PFOA and its salts are surfactants, they tend to spread and coat sample containers and apparatus. Thus unnecessary changing of me test sample container should be avoided, and spike recovery analyses should be performed to assess me degree to which the analyte may be lost due to this phenomenon. Filtration of the sample may be necessary to remove undissolved solids. This should be done only if necessary, since analyte may be lost due to absorption onto the filter. Polypropylene filter media may be preferred for certain perfluorinated surfactants, since absorption is generally less than for other materials.6 In me case of very dilute samples it may be necessary to preconcentrate the sample. This can be accomplished using preconditioned cartridges such as CIS7, Porapak Q, or Tenax. Recovery of spiked blanks and samples should be assessed to determine the efficiency of analyte recovery from such cartridges. Additional sample preparation may be necessary depending on the analytical method chosen for the determination. 53 Types of Water "Clean" water, such as drinking water, usually should not require filtration. Since the concentration of PFOA is likely to be very low, however, it is especially important to avoid contamination during sampling and handling. Preconcentration and pH adjustment may be necessary. Interference from inorganic fluoride may cause problems with a non-specific ^ analytical method, such as total fluorine content. EXP000581 Groundwater and river water may or may not require filtration, depending on the source. Most of the comments pertaining to "clean" water also apply. There may be additional problems created by the presence of biological organisms and .other interfering compounds, especially in river water. Process water, such as that found in fluoropolymer manufacturing facilities or in plants that use fluoropolymers in their manufacturing processes, may contain relatively high concentrations of PPOA or its sates. It is important that the time and place of sampling is carefully noted, since concentrations ofPFOA may fluctuate substantially with time. Filtration may be necessary to remove undissolved solids, but it will probably be necessary to analyze any solids removed, since they may contain sizeable quantities of PFOA as a result of sorption. Interference from other components in the process stream should be considered when choosing an analytical technique. Each type of water mentioned above should be considered as unique, and has its own set of sampling and analytical problems. Seasonal variations might be significant. Again, it is important to verify hold times for analyses of this type. 5.4 Analytical Methods There are many methods that may be applied to the analysis of PFOA and its salts. Factors to be considered when choosing a method include cost and availability of equipment, analytical skin level required for analysts, time requirements for sample preparation and analysis, and any trade-ofis required between sensitivity, accuracy, and precision of measurement These considerations are summarized in Appendix C. Total fluorine content is non-specific to PFOA, but may be adequate for relatively high concentrations in samples where it is known that there are no other sources of fluorine besides PFOA. The organic fluorine must be converted to soluble fluoride ion for many of the more common techniques, and mis will require some type of combustion. It should be noted that perfluorinated compounds, such as PFOA, are difficult to combust completely.7 Analysis of standards and spiked samples are important to ensure that combustion is complete. Gas cbromatography with flame ionizanon (FID), electron capture (BCD), or mass spectroscopic (MSD) detection can be used to determine PFOA. These methods have been reported for me determination of PFOA in blood plasma and urine6'9'10,and may be adapted to water analysis. Since the acid form cannot be chromatographed, it is necessary to first convert the carboxylic acid to an ester. Various procedures can be used for Ihe esterification, and it is important to ensure that the esterification is complete by using spiked samples. These techniques are semi-specific, since the retention times of known standards can serve to identify the materials being analyzed. The lower limit of detection for these techniques is of the order of one to five parts per million by weight They have the advantage of using relatively inexpensive and widely available equipment Nuclear magnetic resonance (^F-NMR) has been reported8to be applicable to PFOA analysis in water with a detection limit of 10 ug/L. It is also semi-specific, but perfluorinated surfactants other than PFOA can interfere with the determination. The presence of branched surfactants can lead to erroneous quantitation; care must be taken to account for the amount of branching. Pre-concentration of samples may be necessary, but derivatization is not. The equipment is expensive and may be available only in larger laboratories. High performance liquid cbromatography (HPLC) has been reported to be applicable to th& analysis perfluorocarboxylic acids in biological samples", and may be adaptable for water analysis. Since PFOA and its salts lack chromophores, it is also necessary to derivatize the sample before analysis when using fluorescence detection. As with gas chromatography, it is semi-specific in that retention time of standards can be used to identify the analyte. HPLC EXP000582 equipment is only moderately expensive and is reported to be more sensitive than gas chromatography.1i Liquid chromatography/tandem mass spectrometry (LC/MS/MS) has been used to determine PFOA in river water8 and human serum.12 It is compound specific and does not require derivadzadon of the sample prior to analysis. It is superior to LC/MS in that it provides an additional dimension, which helps to avoid false positives. A detection limit of 1 pg was reported for water8 and 10 ng/mL for serum.12 It is likely to be ihe most generally applicable technique, especially for trace levels, but the equipment is expensive and likely to be available only in larger laboratories. 5.5 Analytical Method Validation Before generating analytical data on unknown samples with any of die methods mentioned above, it is important to ensure that the method is validated. This is especially important if a method developed for one type of medium, e.g. human serum, is to be adapted to another medium, e.g. water. Lab spiking should be performed to address matrix effects. Blanks are very important for low-level quantitation and minimizing sampling artifacts. Good guidelines for method validation can be found in reference 13. 6.0 Analysis ofAmmoBium Perfluorooctanoate (APFO) in Air Applications of air sampling and analyses methods to the measurement of APFO should include method validation criteria consistent with appropriate regulatory guidance. Due to the potential biphasic nature of APFO and other airborne fluorochemicals consideration of sampling media is critical. Method development should include "zero" air measurements as well as adsorption and desorption efficiencies, and holding time measurements. Preferably the method should be able to discriminate between analyte on particles versus analyte in the vapor phase. There should be "real" blanks, including field blanks taken to the field and exposed to all conditions except for having the air pumped through them. Demonstration of lab capability via analysis of spiked samples and replicates and all associated quality control requirements should be documented. This documentation should include instrumental calibrations and written Standard Operating Procedures (SOPs) or written lab procedures for each step from materials preparation, sampling, analysis, documentation, reporting and deliverables, and data retention. Third party validation or review is desired. Established quality criteria including method performance should be documented (Limit of Quantitation - .LOQ, uncertainties, accuracy, precision, specificity, calibration criteria, blank criteria, matrix or lab control spike criteria, replicates, retention-time window criteria, tuning criteria). Reports of analyses of semivolatile or non-volatile fluorochemicals in air have been limited/ 4'15^ A recent analytical air method exists for the analysis of APFO in workplace atmospheres. This method involves LC/MS/MS analysis of acetone extracts from OSHA Versatile Sampler (OVS) tubes (Occupational Safety and Health Administration, OSHA).14 This method applies to the analysis of "clean" ambient workplace air. Application of the memod to environmental manufacturing emissions sampling or other air matrices would require source specific validation. OVS tubes were used to simultaneously trap fluorochemical particulates and vapors from workplace air. Analytical methods were developed for air samples collected on OVS tubes to quantitatively analyze for both total fluorine, using oxygen bomb combustion/ion selective electrode, and for nineteen analyte specific organofluorochemicals using LC/MS, GC/MS, and 1C (ion cbromatography).14A method validation study was conducted according to 7 EXP000583 the National Institute of Occupational Safety and Health (NIOSH) with minor revisions of the experimental 'design due to specifics of this particular sampling application.16 Method performance for APFO analysis was sufficient in terms of analytical recovery, sampler capacity, storage stability, determination of limits of detection, and precision and bias of me samples. The method combines OVS tube sampling with LC/MS analysis and is applicable for quantitadon of 0.06 - 6 ugs APFO in an OVS tube sample. This method range corresponds to quantitation of APFO in ambient air in the concentration range of 0.001 - 0.1 mg/m3with a 60-liter air sample. 7.0 Determination of Ammonium Perfluorooctanoate (APFO) in Biological Matrices Analyte specific detection of APFO in biological matrices at trace levels (parts per billion by weight) can be accomplished using two primary analytical detection techniques/8'17'and"& w'fl"n) The first technique combines chemical derivatization techniques coupled with gas chromatography/mass spectrometry detection. The second technique combines biological matrix extraction with liquid chromatography/mass spectrometry detection. Biological matrices are highly variable and impact analytical method performance with unpredictable results. Significant differences in method performance criteria can be observed for the same analytical method when it is applied to biological matrix variations of tissue type (e.g., liver versus sera), tissue fractions/components (e.g., whole blood versus serum), and species variation (e.g., rabbit versus rat). Food and Drug Administration (PDA) bioanalytical method validation guidance has been recently published to ensure analytical method performance criteria are denned and are consistent with regulatory method guidelines for data reporting.13 Some recent publications on the determination of APFO in biological matrices show low spike recovery. Low (i.e., <70%) spike recovery percentages may not be appropriate for reporting to regulatory agencies. Analytical method validation plans for "partial" validation of a method that already has successfully met all requirements of a full validation will differ based on the specific method change that requires validation- Examples of specific method changes requiring "partial validation" are given as a list in the FDA guidance document 1. Transfers between laboratories or between analysts 2. Change in analytical methodology (e.g., detection system) 3. Change in anticoagulant in harvesting biological fluid 4. Change in matrix within species (e.g., human plasma to human urine) 5. Change in sample processing procedures 6. Change in species within matrix (e.g., rat plasma to mouse plasma) 7. Change in relevant concentration range 8. Change in instruments and/or software platforms 9. Limited sample volume (e.g., pediatric.study) 10. Rare matrices (e.g., limited number ofindividual samples-endangered species) 11. Selectivity in the presence of concomitant medications 12. Selectivity in the presence of specific metabolites g EXP000584 8.0 Solids The determination of perfluorinated carboxylic acids or their salts in solids can be accomplished directly or indirectly. An indirect method such as the combustion of the material with a Wickbold7 torch for total organic fluoride, followed by determination with fluoride ion- selective electrode measurement, is used to see ifafluorinated compound is present in the solid. Of course the indirect method cannot definitively confirm the presence of any specific fluorinated material. A direct method would probably employ either mermal desorption, derivatizadon, gas chromatography mass spectrometty (GC/MS) or solvent extraction followed by liquid chromatography tandem mass spectrometry (LC/MS/MS). The mass spectrometric methods are specific and definitive since they provide both qualitative and quantitative data. The mass spectrum and retention time are the minimum data needed to identify the presence of a material in a solid. Often with a complex matrix, such as a solid, it is necessary to also characterize the solid since the extraction efficiency of the analyte from its matrix will depend on the composition of the solid and also perhaps how long the solid has been exposed to the analyte of interest It might also be necessary to perform an aging and sequestration study to determine the effect of aging and other components of the matrix. The EPA document "Preparation of Soil Sampling Protocols: Sampling Techniques and Strategies"18notes mat most of the variance involved in soil analysis comes from the sampling and not from the laboratory analysis. With solids ftom a manufacturing process, however, more information on the composition of the solid would be known so that defining the analytical task should be somewhat less complex.' If the solid's matrix contains other fluorinated species, a determination of die concentration and source (decomposition or reaction with the analyte of interest) might also have to be performed to ascertain the "real" concentration. 9.0 Additional Analytical Considerations Fluoropolymer polymerization aids are unique in their physicochemical properties; therefore special care must be taken in sample preparation and analysis. Common predictive models may lead to significantly erroneous results for physieochemical properties: Since these compounds "look" like hydrocarbons, the temptation is to assume similar characteristics for measures of volatility, solubility, etc. This temptation must be resisted and thought given to each step in die method with a full slate of quality assurance (QA) components incorporated into the process ftom sampling through analysis and date acceptance and reduction. Method validation studies need to be conducted to ensure the method is sufficient in terms of analytical recovery, sampler capacity, storage stability, determination of limits of detection, and precision and bias of the samples.16 Before any data are reported, it is important that the work be reviewed for quality and rigor. A good resource is "Guidance for Industry, Bioanalytical Method Validation."13 This document is especially useful when GC or LC methods are employed, and is especially helpful for a single laboratory initiated validation. Table 2 contains some suggested QA components that will add to the defensibility of the data. EXP000585 Table 2. Definitions of Quality Assurance (QA) Criteria QA Criteria ' Definition Blank Calibration A sample subjected to the usual analytical or measurement process to establish a zero or baseline value. A. comparison of a measurement standard, instrument, or item with i standard or instrument of higher accuracy to detect and quantify naccurades and to report or eliminate those inaccuracies by adjustments. Check Standard A. standard prepared independently of die calibration standards and analyzed exactly like the samples. Duplicate Samples Field Blank Laboratory Control Spike two samples taken from, and representative of, the same population and carded through all steps of sampling and analytical procedures in an identical manner. A. blank used to provide information about contanrinante that may be introduced during sample collection, storage, and transport. determines the desorption efficiency of the target analytes from the sampling media. Samples are prepared by spiking blank sampling media, preferably from die same lot of media used in sample collection, with quantities of target analytes commensurate with the ange determined in samples. Laboratory Split Samples Matrix Spike Method Blank two or more representative portions taken from the same sample and analyzed by different laboratories to estimate intedaboratory >recision or variability and die data comparability. A. sample prepared by adding a known mass of a target analyte to a. specified amount of matrix sample for which an independent estimate of the target analyte concentration is available. A blank prepared to represent me sample matrix as closely as >ossible and analyzed exactly like the calibration standards, samples, and quality control (QC) samples. Results of method )lanks provide an estimate of within batch variability of the blank response and an indication of the bias introduced by the analytical procedure. Split Samples Two or more representative portions taken from one sample in the ield and or in the laboratory and analyzed by different analysts or aboratories. Surrogate Spike or Analyte A pure substance wim properties that mimic the analyte of interest Validation Confirmation by examination and provision of objective evidence that die particular requirements for a specific intended use have been fulfilled. Variance (statistical) A measure of the dispersion of a sample or population distribution. EXP000586 10 10.0 References 1 E. Kissa, "Fhiorinated Surfectants and Repellents," Surfactant Science Series, A. T. Hubbard, Ed. Volume 97, Marcel Dekkar, Inc., New York, 2001. 2 B. R. Bhiestein and C.L. Hilton, eds., "Amphoteric Surfactants," Surfactant Science Ser. Vol. 12, Marcel Dekker, New York (1982). 3 Guide to the Safe Handling of Fluoropolymer Dispersions. Fluoropolymer Manufacturers Group, The Society of the Plastics Industry, Inc., Washington, DC, October 2001. 4 ACGM Threshold Limit Values for Chemical Substances and Physical Agents and Biological Exposure Indexes (current edition). ACGffl, 1330 Kemper Meadow Drive, Cincinnati, OH 45240-1634. 5 M. Thompson and M. Ramsey, Analyst, 120,261 (1995). 6 J. Belisle, D. F. Hagen, Analytical Biochemistry, 1980,101,369-376. 7 R. Wickbold, "Quantitative Combustion of Fluorine Containing Organic Substances," Angew. Chem., 1954,66; 173-174. 8 C. A. Moody, W. C. Kwan, J. W. Martin, D. C. Muir, S. A, Mabury, Analytical Chemistry, 2001,73,2200-206. 9 M. YIinen, H. Hanhijarvi, P. Peura, 0. RamQ, Arch. Environ. Contain, and ToxicoL, 1985, 14,713-717. 10 J. Belisle, D. F. Hagen, Analytical Biochemistry, 1978,87,545-555. 11 T.Ohya.N. Kudo, E. Suzuki, Y. Kawashima, J. Chromatogr. B, 1998,720,1-7. 12 C. Sottani, C. Minoia, Rapid Commun. Mass Spectrom., 2002,16,650-654. 13 Guidance for Industry, Bioanalytical Method Validation. U. S. Department of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research (CDER), Center for Veterinary Medicine (CVM), May 2001. 14 W.K. Reagen, et. al., "Analytical Techniques And Method Validation For The Measurement of Selected Semi-Volatile and Non-Volatile Organofluorochemicals In An-," ADHA Journal, manuscript in preparation. 15 J.W. Martin, et. al., "Collection of Airborne Fluorinated Qrganics and Analysis by Gas Chromatography/Chemical lonization Mass Spectrometry," Anal. Chem. 2002,74, 584-590. 16 Guidelines/or Air Sampling and Analytical Method Development and Evaluation, NIOSH Technical Report (May, 1995). 17 K. J. Hansen, L. A. Clemen, M. E. Ellefson, and H. 0. Johnson; "Compound-Specific, Quantitative Characterization of Organic Fluorochemicals in Biological Matrices," Environmental Science & Technology; 2001; 35(4); 766-770. 18 "Preparation of Soil Sampling Protocols: Sampling Techniques and Strategies", EPA 600/R2/128 (1992). 19 T.J. Brice, in "Fluorine Chemistry," J.H. Simons, ed.. Vol. I, Academic Press, New York (1950). 20 D. Lines and H. Sutcliffe, J. Fluorine Chem., 25,505 (1984). 21 J.D. LaZerte, L.J. Hals, T.S. Reid and G.H. Smith, J. Am. Chem. Soc. 75,4525 (1953). 22 H.G. Klein, J.N. Meussdoerffer, and H. Niederpriim, MetaUoberflache 29,559 (1975). 23 V. Glockner, K. Lunkwitz, and D. Prescher, Tenside 26,376 (1989). 24 N. 0. Brace, J. Org. Chem. 27,4491 (1962). 25 P. Mukerjee and K. J. Mysels, Pap. Symp., 1974 ACS Symp. Ser. 9,239 (1975). 26 J. H. Hildebrand, J. M. Prausnitz, and R. L. Scott, "Regular and Related Solutions," p. 204, Van Nostrand Reinhold, New York (1970). 27 E. A. Kauck and A. R. Diesslin, Ind. Eng. Chem. 43,2332 (1951). EXP000587 11 APPENDIX A: Examples ofFlnoropolymer Polymerization Aids Chemical Name Heptafluorobutanoic acid Nonafluoropentanoic acid Ammonium nonafluoropentanoate Undecafluorohexanoic acid Sodium undecafluorohexanoate Ammonium undecafluorohexanoate Tridecafluoroheptanoic acid Potassium tridecafluoroheptanoate Ammonium tridecafluoroheptanoate Pentadecafluorooctanoic acid Potassium pentadecafluorooctanoate Sodium pentadecafluorooctanoate Ammonium pentadecafluorooctanoate Heptadecafluorononaaoic acid Sodium heptadecafluorononanoate Ammonium heptadecafluorononanoate Nonadecafluorodecanoic acid Potassium nonadecafluorodecanoate Sodium nonadecafluorodecanoate Ammonium nonadecafluorodecanoate Heneicosafluoroundecanoic acid Potassium heneicosafluoroundecanoate Sodium heneicosafluoroundecanoate Ammonium heneicosafluoroundecanoate Tricosafluorododecanoic acid Potassium tricosafluorododecanoate Sodium tricosafluorododecanoate Ammonium tricosafluorododecanoate Synonym C4acid CSacid C5NH4salt C6acid CfiNasate C6NH4salt C7acid C7Ksatt C7NH4salt CSacid CSKsatt CSNasaft C8NH4salt C9acid C9Nasaft C9NH4salt ClOacid ClOKsaIt ClONasalt C10NH4salt Cllacid CllKsalt CllNasalt CllNH4salt C12 acid C12 K; salt C12 Na salt C12 NH4 salt CAS# 375-22-4 2706-90-3 68259-11-0 307-24-4 2923-26-4 21615-47-4 375-85-9 21049-36-5 6130-43-4 335-67-1 2395-00-8 335-95-5 3825-26-1 375-95-1 21049-39-8 4149-60-4 335-76-2 51604-85-4 3830-45-3 3108-42-7 2058-94-8 30377-53-8 60871-96-7 4234-23-5 307-55-1 6060-71-5 307-67-5 3793-74-6 Formula C3F7COOH C4F9COOH C4F9COONH4 C5F11COOH C5FllCOONa C5F11COONH4 C6F13COOH C6F13COOK. C6F13C001ffl:4 C7F15COOH C7F15COOK C7F15COONa C7F15COONH4 C8F17COOH C8F17COONa C8F17COONH4 C9F19COOH C9F19COOK C9F19COONa C9F19COONH4 C10E21COOH C10F21COOK C10F21COONa C10F21COONH4 C11F23COOH C11F23COOK CllF23COONa C11F23COONH4 EXP000588 12 Appendix B: General Physical and Chemical Properties a. Thermal Stability Perfluorinated surfactants are remarkably stable; enabling them to withstand conditions which would be too severe for hydrocarbon surfactants.1'16 The C-F bond is one of the strongest known, thus providing the fluorosurfactant stability even at high temperature in the presence of acids, alkali, oxidation and reduction. It has been found that perfluoroalkanecarboxylic acids and perfluoroalkanesulfonic acids are the most stable fluorinated surfactants, while their salts decompose more readily with the cation and Rf chain length apparently of profound influence.1-"'18 b. Chemical Stability Perfluorinated alkanoic and alkanesulfonic acids have excellent chemical stability towards acids, oxidants and alkali.1118'19 Perfluorinated alkanecarboxylic acids are strong acids, similar in strength to mineral acids.20 c. Melting Points The peifluorinated carbon chains of surfactant molecules, as compared to their hydrocarbon analogs, are stiff and inflexible due to the rigidity of the C-F bond.! It is believed that this contributes to their higher melting points, a high Krafft point with reduced solubility in solvents. The Rf chain length and branching of the terminal units have been found to have a marked effect on the melting point21 The size of the cation also has an effect on the melting point The melting points ofperfluorooactanoates with inorganic cations do not increase linearly with increasing size of ionic radii17. This phenomenon is believed to be due to the reduce stability of the salt with increasing size of the ionic radii. d. Solubility The unusual properties of the fluorine atom and the C-F bond also affect the solubilities of the fluorinated surfactants. Perfluoroalkanes are more hydrophobic man their hydrocarbon analogs as shown by their solubility data.22'23 The Rf chain and the hydrophile have an effect on the solubility of the fluorinated surfactant1 The solubility ofperfluoroalkanoic acids decreases with increasing chain length. At 25 C, Cl to C6 perfluorinated alkanoic acids are miscible in water in all proportions whereas the C8 and C10 perfluorinated alkanoic acids are only slightly soluble.24 The same is true for the solubility of alkali metal salts of perfluorinated alkanoic acids in water - i.e. it decreases with increasing chain length. EXP000589 13 Table 3: Physical and Chemical Properties Perfluorobutanoic acid (a) CAS# 375-22-4 Molecular Formula C4HF702 Molecular Weight 214.04 Boiling Point 120 C Melting Point -19.5 C (b) Perfluorovalenc acid (a) 2706-90-3 C5HF902 264.05 127C(c) N/A Undecafluorohexanoic acid (a) Perfluoroheptanoic acid 307-24-4 375-85-9 C6HF1102 C7HF1302 314.06 364.06 157 C at 742 nun (d) 175-177 C 12-14C(f) 54CinCC14(c) Pentadecafluorooctanoic acid (g) Ammonium Pentadecafluorooctanoate (a) Perfluorononan-1-oic acid (a) 335-67-1 3825-26-1 375-95-1 C8HF1502 C8HP1502-H3N C9HF1702 414.07 431.10 464.08 189 "C at 736 nun N/A N/A 55-56<'C 157-165 C (h) 71-77C Perfluoro-N-decanoic acid (a,g) Perfluoroundecanoic acid (a,g) Perfluorododiecanoic acid (a,g) 335-76-2 2058-94-8 307-55-1 C10HF1902 C11HF2102 C12HF2302 514.09 564.09 614.10 2l8C at 740 mm 160 C at 60 mm 245 C at 740 mm 83 - 85 C 96 -101 C 107 -109 C a Beilstein Insdtut as Foerderung der Chemischen Wissenschaften. Copyright 1988-2001 b Henne; Fox; J. Amer. Chem.. Soc., 73,2323 (1953). 0 Benefice-Malouet, S, Blancou, H., Itier, J., Commeyras, A; Synthesis, 647-648 (1991). d E. A. Kauck, and A. R. Diesslin, Ind. Eng. Chem. 43,2332 (1951). e Bnce, etal.; J. Amer. Chem.Soc. 75,2698-2702 (1953). f Rubio, S., Blancou, H., Commeyras, A.; J. Fluorine Chem., 99(2), 171-176 (1999). 8 Data from MSDS sheets h D. Lines and H. Sutcliffe, J. Fluorine Chem.., 25,505-512 (1984). N/A - not available EXP000590 14 Perfluorobutanoic acid (a) Perfluorovaleric acid (a) Undecafluorohexanoic acid (a) Perfluoroheptanoic acid Pentadecafluorooctanoic acid (g) Ammonium Pentadecafluorooctanoate (a) Perfluotononan-1-oic acid (a) Perfluoro-N-decanoic acid (a,g) Perfluoroundecanoic acid (a,g) Perfluorododecanoic acid (a,g) CAS# 375-22-4 Density 1.764 g/cm^d) Refractive Index 1.297 2706-90-3 307-24-4 375-85-9 335-67-1 1.713 g/cm-' (d) 1.762 g/cm1(d) 1.792 g/cm1 (d) N/A 1.294 at R.T. at 589 Dm (e) 1.298 at R.T. at589nm 13119 at 2TC at589nm N/A 3825-26-1 N/A N/A 375-95-1 N/A N/A 335-76-2 N/A N/A 2058-94-8 N/A N/A 307-55-1 N/A N/A Vapor Pressure lOmmHg at20C N/A N/A N/A 0.1 kPa (0.75 mm Hg) N/A N/A N/A N/A N/A Water Solubility N/A N/A N/A N/A 3.4-9.5g/L N/A N/A N/A N/A N/A EXP000591 15 APPENDIX C: Comparison of Available Analytical Techniques for Fhsoropolymers1' Technique Sensitivity Total Fluorine Lowppm 'TNMR* GC/FID Lowppm Lowppm GC/MS* GC/ECD Lowppm Lowppm LC LC/MS* Lowppm ppb LC/MS/MS* Sub-ppb Strencths Non-matrix specific Versatile Specificity Readily available Specificity Sensitivity Sensitivity Specificity Minimal sample preparation Specificity Minimal sample preparation Weaknesses Non-specific Operator dependent Field strength dependent Non-specific Multi-step (derivatization) Multi-step (derivatization) Multi-step (derivatization) Narrow range of linearity Radiation (''Ni source) Detector dependent Possible matrix interference Cost of Instrumentation < $20,000 USD > $100,000 USD $20,000-50,000 USD $50,000100,000 USD $20,000-50,000 USD $20,000-50,000 USD $50,000100,000 USD Timine After Sample Preparation and Instrument Calibration One sample per hour One sample every 8 hours Data acquisition less man 1 hour Date. acquisition less man 1 hour Data acquisition less nian 1 hour Data acquisition less than 1 hour 30 minutes per sample Possible matrix interference > $100,000 USD 30 minutes per sample ' Analytical techniques should be validated for each individual fluoropolymer being analyzed for. * Technique which requires greater or significantly greater operator skill than others listed here. EXP000592 16