Ys. Fung et al., DETERMINATION OF TOTAL ORGANIC-CARBON IN WATER BY THERMAL COMBUSTION-ION CHROMATOGRAPHY, Analytical chemistry, 68(13), 1996, pp. 2186-2190
sensitive method for determining total organic carbon at microgram per
liter levels in industrial, environmental, and drinking waters by the
rmal combustion ion chromatography was developed using tube furnace an
d readily accessable HPLC equipment. To achieve complete oxidation, pe
rsulfate (0.25%) was added to oxidize nonvolatile organic compounds in
solution and cupric oxide heated at 900 degrees C to convert volatile
organic compounds to CO2, which was scrubbed in a 20 mt solution of 5
0 mM KOH with 10 drops of butanol added. The carbonate anion obtained
was determined by nonsuppressed ion chromatography using 0.6 mM potass
ium hydrogen phthalate (KHP) as the eluent. Both surfactants and volat
ile and nonvolatile organic compounds commonly found in environmental
waters give highly repeatable recoveries close to 100%. The detection
limit (S/N = 2) and linear range for a 1 L water sample are 2 mu g of
C L(-1) and 10-2500 mu g of C L-l, respectively, and they can be adjus
ted using samples ranging from 100 mt to 2 L. Good repeatablity (RSD l
ess than 10%) and close to 100% recoveries were obtained for IMP added
to real samples such as deionized, mineral, tap, and river water and
seawater, Compared with the ASTM D2579 method, the method developed is
3 orders of magnitude more sensitive, more accurate, and reliable in
determining samples with low total organic carbon values and more flex
ible in adjusting the linear range and sensitivity using variable samp
le sizes.