Evaluation of Long-Term Flow Controller for Monitoring Gases and Vapors in Buildings Impacted by Vapor Intrusion.

This study evaluated the use of a long-term capillary flow controller paired with an evacuated canister for indoor air exposure monitoring in a vapor intrusion (VI) environment with trichloroethylene in comparison to the traditional method utilizing a diaphragm flow controller. Traditionally, air sampling with 6 L evacuated canisters equipped with diaphragm flow controllers has been best suited for 8 to 24 h samples. New advances in capillary flow controllers can extend sampling to up to 3 weeks by reducing flow rates to 0.

Enhanced Recovery of Per- and Polyfluoroalkyl Substances (PFASs) from Impacted Soils Using Heat Activated Persulfate.

Varying transport potential of cationic, zwitterionic, and anionic per- and polyfluoroalkyl substances (PFASs) may pose challenges for remediation of aqueous film forming foam (AFFF) impacted sites, particularly during groundwater extraction. Slow desorption of stronger sorbing, zwitterionic, and cationic PFASs may cause extended remediation times and rebound in aqueous PFAS concentrations. Persulfate oxidation has the potential to convert a complex mixture of PFASs into a simpler and more recoverable mixture of perfluoroalkyl acids (PFAAs).

Slow-release permanganate versus unactivated persulfate for long-term in situ chemical oxidation of 1,4-dioxane and chlorinated solvents.

The objective of this research was to evaluate slow-release permanganate and unactivated persulfate for in situ treatment of dioxane and associated chlorinated solvents. Laboratory batch studies with unactivated persulfate in deionized water or in soil and groundwater demonstrated dioxane removal with pseudo second-order rate constants ranging from 10 to 10 M s. Flow-through column studies demonstrated over 99% dioxane removal with slow-release unactivated persulfate but not with slow-release permanganate.

Evaluation and Management Strategies for Per- and Polyfluoroalkyl Substances (PFASs) in Drinking Water Aquifers: Perspectives from Impacted U.S. Northeast Communities.

Background: Multiple Northeast U.S. communities have discovered per- and polyfluoroalkyl substances (PFASs) in drinking water aquifers in excess of health-based regulatory levels or advisories.

Field demonstration of polymer-amended in situ chemical oxidation (PA-ISCO).

The methods and results of the first field-scale demonstration of polymer-amended in situ chemical oxidation (PA-ISCO) are presented. The demonstration took place at MCB CAMLEJ (Marine Corps Base, Camp Lejeune) Operable Unit (OU) 15, Site 88, in Camp Lejeune, North Carolina between October and December 2010. PA-ISCO was developed as an alternative treatment approach that utilizes viscosity-modified fluids to improve the in situ delivery and distribution (i.

Release of chromium from soils with persulfate chemical oxidation.

An important part of the evaluation of the effectiveness of persulfate in situ chemical oxidation (ISCO) for treating organic contaminants is to identify and understand its potential impact on metal co-contaminants in the subsurface. Chromium is a redox-sensitive and toxic metal the release of which poses considerable risk to human health. The objective of this study was to investigate the impact of persulfate chemical oxidation on the release of chromium from three soils varying in physical-chemical properties.

Comparative study on oxidative treatments of NAPL containing chlorinated ethanes and ethenes using hydrogen peroxide and persulfate in soils.

The goal of this study was to assess the oxidation of NAPL in soil, 30% of which were composed of chlorinated ethanes and ethenes, using catalyzed hydrogen peroxide (CHP), activated persulfate (AP), and H(2)O(2)-persulfate (HP) co-amendment systems. Citrate, a buffer and iron ligand, was amended to the treatment system to enhance oxidative treatment. Four activation/catalysis methods were employed: (1) oxidant only, (2) oxidant-citrate, (3) oxidant-iron(II), and (4) oxidant-citrate-iron(II).

Experimental design of diffusion and desorption of contaminant in heterogeneous media.

Storage of contaminants in low permeability media (LPM) presents a great challenge for prediction of remediation effectiveness and efficiency. The reason lies in the contaminants' complex behaviors within heterogeneous media. Both interparticle and intraparticle diffusion contribute to the difficulty of precise site assessment.

Enhanced permanganate in situ chemical oxidation through MnO2 particle stabilization: evaluation in 1-D transport systems.

In situ chemical oxidation using permanganate is an increasingly employed approach to organic contaminant remediation at hazardous waste sites. Manganese dioxide (MnO2) particles form as a by-product of the reaction of permanganate with contaminants and naturally-reduced subsurface materials. These particles are of interest because they have the potential to deposit in the subsurface and impact the flow regime in/around permanganate injection, including the well screen, filter pack, and the surrounding subsurface formation.

Control of manganese dioxide particles resulting from in situ chemical oxidation using permanganate.

In situ chemical oxidation using permanganate is an approach to organic contaminant site remediation. Manganese dioxide particles are products of permanganate reactions. These particles have the potential to deposit in the subsurface and impact the flow-regime in/around permanganate injection, including the well screen, filter pack, and the surrounding subsurface formation.

Coupling permanganate oxidation with microbial dechlorination of tetrachloroethene.

For sites contaminated with chloroethene non-aqueous-phase liquids, designing a remediation system that couples in situ chemical oxidation (ISCO) with potassium permanganate (KMnO4) and microbial dechlorination may be complicated because of the potentially adverse effects of ISCO on anaerobic bioremediation processes. Therefore, one-dimensional column studies were conducted to understand the effect of permanganate oxidation on tetrachloroethene (PCE) dechlorination by the anaerobic mixed culture KB-1. Following the confirmation of PCE dechlorination, KMnO4 was applied to all columns at a range of concentrations and application velocities to simulate varied distances from oxidant injection.

Association of cadmium with MnO2 particles generated during permanganate oxidation.

Particle filtration and cadmium sorption studies were performed at selected time points during reaction of potassium permanganate with trichloroethylene under varied reaction matrix conditions. The purpose of the studies was to determine the potential impact of manganese oxides particle generation, a by-product of the permanganate reaction, on subsurface metal mobility, with cadmium serving as a representative metal of interest in the environment. Results of the studies indicate that the association of cadmium with the manganese oxides is a function of (1) particle concentration, (2) pH, (3) the presence of calcium in the reaction matrix, and (4) the rate of particle generation and agglomeration.

Geochemical effects on metals following permanganate oxidation of DNAPLs.

The application of in situ chemical oxidation for dense, nonaqueous phase liquid (DNAPL) remediation requires delivery of substantial levels of oxidant chemicals into the subsurface to degrade target DNAPLs and to satisfy natural oxidant demand. This practice can raise questions regarding changes in subsurface conditions, yet information regarding potential effects, especially at the field scale, has been lacking. This paper describes an evaluation of the effects on metals associated with in situ chemical oxidation using potassium permanganate at Launch Complex 34 (LC34), Cape Canaveral Air Station, Florida.