Perfluoroalkyl and polyfluoroalkyl substances thermal desorption evaluation. Issue 4 (11th September 2019)

• Record Type: Journal Article
• Authors: Crownover, Emily; Oberle, Daniel; Kluger, Mark; Heron, Gorm
• Is Part Of: Remediation. Volume 29:Issue 4(2019)
• Page Start: 77
• Page End: 81
• Publication Date: 2019-09-11
• Subjects: Sanitary engineering -- Periodicals; 628
• DOI: 10.1002/rem.21623
• Languages: English
• ISSNs: 1051-5658

Abstract

Abstract: Per‐ and polyfluoroalkyl substances (PFAS) are highly resistant to biotic and abiotic degradation and can withstand very high temperatures before breaking down. The storage of PFAS‐impacted water and sediments in a holding pond or stockpiled investigation or remedial action‐derived waste is occurring on an increasing number of sites. The most common PFAS water treatment options include granular‐activated carbon and resins and the most common soil treatment options have been primarily limited to excavation, offsite incineration, and, in some cases, soil stabilization. An increasing number of states across the United States are establishing part per trillion PFAS guidance levels for drinking water. Removing PFAS from soils removes PFAS source impacts to groundwater. In this study, volatilization of PFAS from soil treated using in situ thermal heating is evaluated as a treatment method to achieve a high degree of PFAS removal from soils. The evaluation of temperatures needed to achieve removal is described. To minimize vapor treatment required for PFAS thermal remediation, a scrubber was incorporated into the treatment train to transfer PFAS to the liquid phase in a concentrated, low‐volume solution. Vapor‐liquid equilibrium behavior and the extent of PFAS volatilization from impacted soil over a range of temperatures were evaluated. Results showed that heating soil to 350°C and 400°C reduces PFAS soil concentrations by 99.91% and 99.998%, respectively. It was also confirmed that sulfonate‐based PFAS generally required higher temperatures for volatilization to occur than carboxylate‐based PFAS.