FINAL REPORT - serdp-estcp.org

1 FINAL REPORT Extending The Applicability of Compound-Specific Isotope analysis To Low Concentrations Of 1,4-Dioxane SERDP Project ER-2535 FEBRUARY 2017 Peter Bennett Haley & Aldrich, Inc. Distribution Statement A Page Intentionally Left Blank This REPORT was prepared under contract to the Department of Defense Strategic Environmental Research and Development Program (SERDP). The publication of this REPORT does not indicate endorsement by the Department of Defense, nor should the contents be construed as reflecting the official policy or position of the Department of Defense.

2 Reference herein to any specific commercial product, process, or service by trade name, trademark, manufacturer, or otherwise, does not necessarily constitute or imply its endorsement, recommendation, or favoring by the Department of Defense. Page Intentionally Left Blank REPORT DOCUMENTATION PAGE Form Approved OMB No. 0704-0188 Public reporting burden for this collection of information is estimated to average 1 hour per response, including the time for reviewing instructions, searching existing data sources, gathering and maintaining the data needed, and completing and reviewing this collection of information.

3 Send comments regarding this burden estimate or any other aspect of this collection of information, including suggestions for reducing this burden to Department of Defense, Washington Headquarters Services, Directorate for Information Operations and Reports (0704-0188), 1215 Jefferson Davis Highway, Suite 1204, Arlington, VA 22202-4302. Respondents should be aware that notwithstanding any other provision of law, no person shall be subject to any penalty for failing to comply with a collection of information if it does not display a currently valid OMB control number.

4 PLEASE DO NOT RETURN YOUR FORM TO THE ABOVE ADDRESS. 1. REPORT DATE (DD-MM-YYYY)26-01-20182. REPORT TYPESERDP FINAL REPORT Report3. DATES COVERED (From - To)Dec 2014 Jan 20184. TITLE AND SUBTITLEF inal REPORT 5a. CONTRACT NUMBER W912HQ-14-P-0143 Extending the Applicability of Compound-Specific Isotope 5b. GRANT NUMBER N/A analysis to Low Concentrations of 1,4-Dioxane5c. PROGRAM ELEMENT NUMBER N/A (S)Bennett, Peter 5d. PROJECT NUMBER ER-2535 Aravena, Ramon 5e. TASK NUMBER N/A 5f. WORK UNIT NUMBERN/A 7.

5 PERFORMING ORGANIZATION NAME(S) AND ADDRESS(ES) 8. PERFORMING ORGANIZATION REPORTNUMBERH aley & Aldrich, Inc. 1956 Webster Street Suite 300 Oakland, California 94612 41703-0049. SPONSORING / MONITORING AGENCY NAME(S) AND ADDRESS(ES)10. SPONSOR/MONITOR S ACRONYM(S)Strategic Environmental Research and Development ProgramSERDP4800 Mark Center Drive, Suite 17D08 Alexandria, VA 22350-360511. SPONSOR/MONITOR S REPORTNUMBER(S)12. DISTRIBUTION / AVAILABILITY STATEMENTA pproved for public release; distribution is unlimited 13.

6 SUPPLEMENTARY NOTESN/A 14. ABSTRACTThe objective of this work was to develop a reliable method to perform compound-specific isotope analysis (CSIA) on low aqueous concentrations (1 g/L) of 1,4-dioxane in groundwater and then apply it to investigate 1,4-dioxane biodegradation. It was determined that grams of a synthetic carbonaceous sorbent, when added to a 40 mL vial containing aqueous 1,4-dioxane in the 10 to 100 g/L range, could adsorb more than 99 percent of the 1,4-dioxane from solution. The 1,4-dioxane was successfully recovered from the dried solid sorbent by thermal desorption into a gas chromatograph with isotope ratio mass spectrometry.

7 The method was successfully applied to samples at concentrations in the 1 g/L range. It is anticipated that the CSIA method will be applied to demonstrate the biodegradation of 1,4-dioxane in the 1-10 0 g/L range. The method is likely to be adaptable to other contaminants and media ( ,air and soil), thereby extending the applicability of CSIA to possibly document degradationprocesses that may be occurring at much lower concentrations in the SUBJECT TERMS1,4- dioxane, compound-specific isotope analysis , CSIA, Ambersorb 560, thermal desorption, GC-IRMS 16.

8 SECURITY CLASSIFICATION OF:17. LIMITATIONOF ABSTRACT18. NUMBEROF PAGES19a. NAME OF RESPONSIBLE PERSONP eter Bennett a. REPORTUNCLASS b. ABSTRACTUNCLASS c. THIS PAGEUNCLASS UNCLASS 53 19b. TELEPHONE NUMBER (include area code)(510)879-4547 Standard Form 298 (Rev. 8-98) Prescribed by ANSI Std. Intentionally Left Blank i LIST OF TABLES iiiLIST OF FIGURES iiiLIST OF ACRONYMS ivABSTRACT viACKNOWLEDGEMENTS INTRODUCTION1 Degradation of 1,4-Dioxane 2 Compound Specific Isotope analysis for Documenting Degradation 2 TECHNICAL SCOPE OF PROJECT ER-2535 3 Task 1 Method Development 3 Task 2 Assessment of Isotope Fractionation 3 Task 3 CSIA of 1,4-Dioxane and CVOCs during Cometabolic Degradation 4 Task 4 CSIA of 1.

9 4-Dioxane and CVOCs at Field Sites 4 Task 5 Project Management and Reporting 4 AND TASK 1 METHOD DEVELOPMENT6 Tests 1-4: Micro-Column Sorption with Acetone Elution 7 Test 5: Column Sorption with Thermal Recovery 7 Tests 6-14: Column Sorption with Either Solvent Elution or Thermal Desorption 8 Equilibrium Sorption of 1,4-Dioxane 10 TASK 2 ASSESSMENT OF ISOTOPE FRACTIONATION 11 Determination of Carbon Isotope Ratios of 1,4-Dioxane by Direct Injection GC-IRMS 12 Determination of Carbon Isotope Ratios of 1,4-Dioxane by Thermal Desorption GC-IRMS 12 Determination of Hydrogen Isotope Ratios of 1,4-Dioxane by Thermal Desorption GC-IRMS 12 TASK 3 CSIA OF 1.

10 4-DIOXANE DURING COMETABOLIC DEGRADATION 12 Microcosm Studies for Determining Enrichment Factors 13 Field Study of Aerobic Cometabolic Degradation 14 TASK 4 CSIA OF 1,4-DIOXANE AT FIELD SITES 15 ii Vandenberg Air Force Base Site 24 15 Cape Canaveral Air Force Station Sites 16 4. RESULTS AND DISCUSSION 17 analysis OF STABLE CARBON AND HYDROGEN ISOTOPE RATIOS OF 1,4-DIOXANE AT LOW CONCENTRATIONS IN WATER SAMPLES 17 Stable Carbon Isotope analysis of 1,4-Dioxane 18 Stable Hydrogen Isotope analysis of 1,4-Dioxane 19 MICROCOSM STUDIES ON ENRICHMENT OF CARBON AND HYDROGEN ISOTOPE RATIOS DURING AEROBIC COMETABOLIC DEGRADATION OF 1,4-DIOXANE 21 ASSESSMENT OF CARBON AND HYDROGEN ISOTOPE RATIOS DURING AEROBIC COMETABOLIC DEGRADATION OF 1.