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CHAPTER 22

                           ENVIRONMENTAL REMEDIATION OF VOLATILE
                           ORGANIC COMPOUNDS





                           RON FALTA
                           Clemson University, Clemson, SC, USA


                           22.1  INTRODUCTION

                           Over the past 25 years, groundwater and subsurface contamination by volatile
                           organic compounds (VOCs) has emerged as a widespread problem in industrialized
                           countries. This class of compounds is broad, and it includes a variety of com-
                           mon organic chemicals such as aromatic hydrocarbons (e.g., benzene, toluene,
                           and xylenes) aliphatic hydrocarbons, (e.g., pentane, hexane, and cyclohexane)
                           and halogenated hydrocarbons (e.g., carbon tetrachloride, tetrachloroethylene, and
                           trichloroethylene). These chemicals are widely used as chemical feedstocks, as
                           cleaning solvents and degreasers, and, in the case of hydrocarbons, as fuels.
                             These chemicals, besides having a high vapor pressure, tend to have low aqueous
                           solubilities, on the order of 50 to 2000 mg/l. The low solubility of most VOCs tends
                           to result in high Henry’s constants, and strong partitioning into the gas phase from
                           the aqueous phase.
                             Unfortunately, many of these common chemicals are also toxic, and have very
                           low maximum contaminant levels (MCLs) in drinking water. For example, benzene,
                           which is one of the most common industrial chemicals in the world, has an aqueous
                           solubility of about 1760 mg/l, yet the United States MCL is only 5 ug/l.
                             Due to their low aqueous solubility, VOCs typically exist as nonaqueous phase
                           liquids (NAPLs), and they are often released to the environment in this form. The
                           hydrocarbon fuel mixtures such as gasoline, kerosene, diesel, jet fuel, and fuel oil
                           form LNAPLs (lighter than water NAPLs), while the chlorinated cleaning solvents
                           form DNAPLs (denser than water NAPLs). Due to capillary trapping, complete
                           removal of NAPLs from the subsurface by mobilization is nearly impossible, and
                           conventional fluid pumping operations typically leave behind NAPL saturations of
                           5 to 25%.


                                                           353
                           C. Ho and S. Webb (eds.), Gas Transport in Porous Media, 353–370.
                           © 2006 Springer.
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