{Reference Type}: Journal Article
{Title}: Fractionation of oil sands-process affected water using pH-dependent extractions: a study of dissociation constants for naphthenic acids species.
{Author}: Huang R;Sun N;Chelme-Ayala P;McPhedran KN;Changalov M;Gamal El-Din M;
{Journal}: Chemosphere
{Volume}: 127
{Issue}: 0
{Year}: May 2015
{Factor}: 8.943
{DOI}: 10.1016/j.chemosphere.2014.11.041
{Abstract}: The fractionation of oil sands process-affected water (OSPW) via pH-dependent extractions was performed to quantitatively investigate naphthenic acids (NAs, CnH2n+ZO2) and oxidized NAs (Ox-NAs) species (CnH2n+ZO3 and CnH2n+ZO4) using ultra-performance liquid chromatography time-of-flight mass spectrometry (UPLC-TOFMS). A mathematical model was also developed to estimate the dissociation constant pKa for NAs species, considering the liquid-liquid extraction process and the aqueous layer acid-base equilibrium. This model provides estimated dissociation constants for compounds in water samples based on fractionation extraction and relative quantification. Overall, the sum of O2-, O3-, and O4-NAs species accounted for 33.6% of total extracted organic matter. Accumulative extracted masses at different pHs revealed that every oxygen atom added to NAs increases the pKa (i.e., O2-NAs<O3-NAs<O4-NAs), indicating that the additional O atoms exist as -OH in O3- and O4-NAs. Molecule electron-withdrawing groups such as double bonds and aromatic groups, as indicated by higher carbon and -Z number, may be responsible for the lower pKa of O2-, O3-, and O4-NAs. The model obtained estimated pKa values of 3.5 for O2-NAs, 4.8 for O3-NAs, and 6.8 for O4-NAs via nonlinear regression curve fittings. These pKa values are valuable physicochemical parameters for environmental engineering applications targeting OSPW NAs treatment.