Research Article

Study on Dicarboxylic Acids in Aerosol Samples with Capillary Electrophoresis

Table 1

Method optimization data: the calibration of the DCAs. Experimental conditions: 4 mM PDA + 0.5 mM MTAH, pH 11.0; indirect detection at 310/266 nm (pilot/reference wavelength); sample injection for 6 sec. at 50 mbar; separation voltage −24 kV; analysis time 5 min.

Dicarboxylic acidsConcentration calibration equation Calibration range* [pg]Minimum amounts (MDL)** [pg]

Oxalic acid (C2) 0.99961.03*–102.618.3**
Malonic acid (C3) 0.93371.19–118.920.1
Succinic acid (C4) 0.99941.02–102.615.2
Glutaric acid (C5) 0.93671.02–101.611.4
Adipic acid (C6) 0.99891.01–100.811.9
Pimelic acid (C7) 0.99891.02–102.012.2
Suberic acid (C8) 0.99781.0–100.015.2
Azelaic acid (C9) 0.99911.07–107.317.4
Sebacic acid (C10) 0.99931.03–103.030.5
Mandelic acid (MA, IS1) 0.9908ndnd
Trichloroacetic acid (TCA, IS2) 0.9778ndnd

Example about the calculations: Injection of 0.5 p.s.i. for 6 sec. 6 nL sample into the capillary, calculated with program CE Expert Lite; corresponds: 0.167 mg/L standard sample that is injected for 6 s at 0.5 p.s.i.; signal-to-noise ratio (S/N) used is 3. Oxalic acid in detection: 1.03 pg.
**Calculation made by similar ways as in calibration; signal-to-noise ratios (S/N) is 3; Oxalic acid in the filter sample: 3.05 mg/L.