2. ENVIRONMENTAL ChEMISTRy & TEChNOLOGy 2.1. Lectures
2. ENVIRONMENTAL ChEMISTRy & TEChNOLOGy 2.1. Lectures
2. ENVIRONMENTAL ChEMISTRy & TEChNOLOGy 2.1. Lectures
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Chem. Listy, 102, s265–s1311 (2008) Environmental Chemistry & Technology<br />
P14 INDOOR AEROSOL ExAMINING<br />
ADRIAnA EŠTOKOVá, nADEŽDA ŠTEVULOVá and<br />
LEnKA KUBInCOVá<br />
Technical University of Košice, Civil Engineering Faculty,<br />
Institute of Building and Environmental Engineering, Vysokoškolská<br />
4, 042 00 Košice, Slovak Republic,<br />
Adriana.Estokova@tuke.sk<br />
Introduction<br />
Aerosol particles are generally considered to be one of<br />
the principal indoor risk factors. Operation, number and behavior<br />
of occupancy i.e. type, emission intensity and amount of<br />
indoor contamination sources (building materials, combustion<br />
processes, smoking, cleaning) 1,2 determine temporal and<br />
spatial variations of indoor aerosol distribution. The particulate<br />
matter (PM) cause the negative health effect, when they<br />
are inhaled and deposited in the respiratory tract 3 .<br />
This paper is primarily concerned with suspended PM 10<br />
concentrations and indoor settled PM monitoring with regard<br />
to the chemical composition and shape of PM 10 particles.<br />
Experimental<br />
M e t h o d s<br />
Suspended particulate matter investigation was focused<br />
on thoracic fraction PM 10 monitoring in various types<br />
of residential and non-residential buildings. Measurement<br />
includes integral particles sampling onto a collection material<br />
(membrane filter Synpor 0,8 µm pore size, 35 mm in diameter)<br />
by sampling equipment VPS 2000 (Envitech, Trenčín) at<br />
air flow of 960 dm 3 h –1 during sampling period of approximately<br />
24 hours. The sampling was carried out in the middle<br />
of the room at the height of 1,500 mm from the floor. The<br />
windows and the door were closed during the monitoring<br />
period. The particulate mass concentrations were determined<br />
by gravimetric method from the increase of filter weight.<br />
Because of minimisation of humidity interference, the filters<br />
were dried at 105 °C for 8 h before and after sampling and<br />
than were equilibrated at a constant temperature and humidity<br />
(e.g. 20 °C and 50 % RH) for 24 h before and after sampling.<br />
The monitoring of indoor settled PM was performed<br />
in selected flat building. Sampling was carried out by passive<br />
methods based on PM settling into Petri dishes during<br />
28 days. The particle surface concentrations were determined<br />
by gravimetric method.<br />
The PM 10 samples were characterized by scanning<br />
electron microscopy/energy-dispersive X-ray analysis (SEM/<br />
EDX) and atomic absorption spectroscopy (AAS) as the main<br />
techniques. Particle morphology was determined by SEM on<br />
the equipment Tesla BS 340. The elemental EDX analysis<br />
were carried out on the micro-analytical system LInK ISIS<br />
300 (Oxford Instruments) operating in secondary mode at a<br />
potential 25 kV and at extension 600–30,000. The chemical<br />
analysis of the selected metals samples content was realised<br />
by SpectrAA-30 (Varian).<br />
s361<br />
Results<br />
The results of indoor PM 10 monitoring in different types<br />
of residential and non-residential buildings are illustrated as<br />
average mass concentrations in the Fig. 1.<br />
Fig. 1. The average mass concentrations of PM10 in residential<br />
(A) and non-residential (b) buildings: A1 – single family residences,<br />
A2 – flat-residences, B1 – school buildings; B2 – offices;<br />
b3 – commercial buildings; b4 – buildings for culture and ntertainment,<br />
b5 – hospitals and sanitary facilities<br />
The highest mass PM 10 concentration was observed in<br />
non-residential public buildings. The PM 10 hygienic limit for<br />
indoor air in Slovak republic – 50 µg m –3 was exceeded in all<br />
monitored types of residential and non-residential buildings<br />
excepting B2 (offices) and B5 (hospitals). The concentrations<br />
of settled PM were measured at various heights and were ranged<br />
from 21.0 μg cm –2 to 86.6 µg cm –2 . The trend of gradual<br />
decreasing of particulate matter occurrence with the raise of<br />
height was observed (Fig. <strong>2.</strong>).<br />
Fig. <strong>2.</strong> Average mass surface concentration of settled PM in dependence<br />
on the height<br />
The mass concentrations of metals in PM 10 samples<br />
investigated by AAS are summarised in Table I.<br />
The obtained mass concentrations of metals in indoor<br />
particle samples correspond with those of in typical urban<br />
aerosol 5 . The individual particles in irregular shape of the<br />
various particle size as well as particles aggregates were<br />
observed on the SEM micrographs (Fig. 3.).