The work presented here is a study of the behaviour of the particulate
phase of ETS under controlled laboratory conditions and in real indoo
r environments with the aim of providing information for assessment of
human exposure to ETS. This paper reports investigations of the size
distribution of ETS and changes to the distribution with time under a
range of environmental conditions. Measurements were performed using t
wo instruments, the Scanning Mobility Particle Sizer and the Aerodynam
ic Particle Sizer, which enabled the determination of the precise loca
tions of ETS peaks at frequent short time intervals. While total parti
cle concentrations or changes in concentrations are not specific marke
rs of ETS, peaks related to ETS in the spectral distribution of atmosp
heric particles, for a properly designed experiment, are. The presence
and locations of these peaks are characteristic of ETS in indoor envi
ronments and are clearly distinguishable from the background particle
distribution. It is demonstrated that an initial ETS size distribution
in an indoor environment about 10 min after generation by a human smo
ker has a major peak in the submicron range between 60 and 90 nm. The
location of the peak does not depend on the relative humidity, but doe
s depend on the way the cigarette is smoked. An increase in particle s
ize in the range of 20 to 50%, takes place in the first 30 to 60 min a
fter ETS generation and then remains unchanged for the duration of the
experiment. A decrease in particle size (shrinkage), was not observed
during these experiments. Particle shrinkage has been reported in the
literature. Both the SS and the MS smoke reveal bimodal size distribu
tion. In both cases the most significant, in terms of particle numbers
, is the submicron peak. Natural ventilation, which is the most common
type of ventilation for residences, is often not sufficient for effec
tively reducing human exposure to ETS. Controlled chamber experiments
are useful for investigations of general trends in ETS size distributi
on and concentration and the results from such experiments, in most ca
ses, correlate well with those from real indoor measurements. There ar
e however, aspects which show certain differences between the two type
s of experiments. These differences indicate that chamber experiments
can not fully simulate indoor measurements, and results from such expe
riments should be treated with caution when applied to exposure assess
ment. (C) 1997 Elsevier Science B.V.