GAS PARTICLE PARTITIONING OF ORGANIC-COMPOUNDS TO ENVIRONMENTAL TOBACCO-SMOKE - PARTITION-COEFFICIENT MEASUREMENTS BY DESORPTION AND COMPARISON TO URBAN PARTICULATE MATERIAL/
Ck. Liang et Jf. Pankow, GAS PARTICLE PARTITIONING OF ORGANIC-COMPOUNDS TO ENVIRONMENTAL TOBACCO-SMOKE - PARTITION-COEFFICIENT MEASUREMENTS BY DESORPTION AND COMPARISON TO URBAN PARTICULATE MATERIAL/, Environmental science & technology, 30(9), 1996, pp. 2800-2805
Certain organic compounds in environmental tobacco smoke (ETS) can cau
se respiratory diseases and lung cancers. The behavior and health effe
cts of EIS will depend upon how each of these compounds is distributed
between the gas and the particulate phases. ETS particles were collec
ted on a filter. Semivolatile organic compounds were desorbed from the
filter at 20 degrees C using a Row of clean nitrogen at 60% relative
humidity. The desorption was followed with time. Volatile, lower molec
ular weight compounds were released quickly; less volatile compounds w
ere desorbed slowly. A diffusion model was used to estimate gas/partic
le partition coefficient (K-p) values. The n-alkane and polycyclic aro
matic hydrocarbon (PAH) data agreed with prior measurements for ETS by
another method. New data for four nitrogen-containing compounds were
obtained. At a given pure compound vapor pressure, PAHs were sorbed mo
re strongly than the n-alkanes. The K-p value for nicotine was unusual
ly large, probably due to a significant degree of protonation of the n
icotine in the EIS phase. For carbazole, however, which cannot be prot
onated, K-p was very similar to what would be predicted for a PAH of t
he same vapor pressure. After normalization for the fraction of organi
c matter in the particulate phase, the ETS data for PAHs agreed well w
ith data for PAHs sorbing to urban particulate material (UPM). This is
consistent with the interpretation that partitioning to both ETS acid
UPM is absorptive in nature.