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In situ chemical oxidation of residual LNAPL and dissolved‐phase fuel hydrocarbons and chlorinated alkenes in groundwater using activated persulfate
Author(s) -
Siegal Joan,
Rees Assaf A.,
Eggers Karl W.,
Hobbs Rebecca L.
Publication year - 2009
Publication title -
remediation journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.762
H-Index - 27
eISSN - 1520-6831
pISSN - 1051-5658
DOI - 10.1002/rem.20199
Subject(s) - persulfate , sodium persulfate , chemistry , environmental chemistry , groundwater , dissolution , sodium hydroxide , nuclear chemistry , geology , organic chemistry , catalysis , geotechnical engineering
A treatablity study (TS) was conducted to evaluate the efficacy of in situ chemical oxidation (ISCO) using activated persulfate, alone and in combination with air sparging (AS), for treating a source area contaminated with residual light nonaqueous‐phase liquid (LNAPL), dissolved‐phase fuel hydrocarbons (HCs), and dissolved‐phase chlorinated alkenes at Edwards Air Force Base (AFB), California. The TS was implemented in two phases. Phase I included injecting a solution of sodium persulfate and sodium hydroxide (NaOH) into groundwater via an existing well where residual LNAPL and dissolved‐phase contaminants were present. Because the results of Phase I indicated a limited distribution of the activated persulfate, Phase II was performed to assess whether AS could enhance the distribution of the sodium persulfate. Each phase was followed by groundwater monitoring and sampling at the injection well and at three monitoring wells, located 20 to 44 feet from the injection well. Results from Phases I and II of the TS indicated that (1) alkaline‐activated persulfate was effective in promoting the dissolution of LNAPL and the degradation of dissolved‐phase contaminants, but only at the injection well; (2) the addition of AS was effective in enhancing the radius of persulfate distribution from less than 20 feet to greater than 44 feet, and (3) persulfate alone (i.e., not in an activated state) was effective in reducing the concentrations of dissolved‐phase fuel HC and chlorinated alkenes. © 2009 Wiley Periodicals, Inc.