Tunga Salthammer

Indoor aerosols: from personal exposure to risk assessment

Motivated by growing considerations of the scale, severity, and risks associated with human exposure to indoor particulate matter, this work reviewed existing literature to: (i) identify state-of-the-art experimental techniques used for personal exposure assessment; (ii) compare exposure levels reported for domestic/school settings in different countries (excluding exposure to environmental tobacco smoke and particulate matter from biomass cooking in developing countries); (iii) assess the contribution of outdoor background vs indoor sources to personal exposure; and (iv) examine scientific understanding of the risks posed by personal exposure to indoor aerosols. Limited studies assessing integrated daily residential exposure to just one particle size fraction, ultrafine particles, show that the contribution of indoor sources ranged from 19% to 76%. This indicates a strong dependence on resident activities, source events and site specificity, and highlights the importance of indoor sources for total personal exposure. Further, it was assessed that 10-30% of the total burden of disease from particulate matter exposure was due to indoor-generated particles, signifying that indoor environments are likely to be a dominant environmental factor affecting human health. However, due to challenges associated with conducting epidemiological assessments, the role of indoor-generated particles has not been fully acknowledged, and improved exposure/risk assessment methods are still needed, together with a serious focus on exposure control.

Formaldehyde in the Ambient Atmosphere: From an Indoor Pollutant to an Outdoor Pollutant?

Formaldehyde has been discussed as a typical indoor pollutant for decades. Legal requirements and ever-lower limits for formaldehyde in indoor air have led to a continual reduction in the amount of formaldehyde released from furniture, building materials, and household products over many years. Slowly, and without much attention from research on indoor air, a change of paradigm is taking place, however. Today, the formaldehyde concentrations in outdoor air, particularly in polluted urban areas, sometimes already reach indoor levels. This is largely a result of photochemical processes and the use of biofuels. In the medium term, this development might have consequences for the way buildings are ventilated and lead to a change in the way we evaluate human exposure.

Ultra-fine particles release from hardcopy devices: Sources, real-room measurements and efficiency of filter accessories

The release of ultra-fine particles (UFP, d < 0.1 microm) from hardcopy devices such as laser printers into the indoor environment is currently a topic of high concern. The general emission behavior of a printer can be examined by conducting emission test chamber measurements with particle-counting devices. Chamber experiments with modified laser printers operated without toner or paper also revealed UFP emissions. On the basis of these results we reasonably doubt the opinion that UFPs primarily originate from the toner. Instead, the high-temperature fuser unit is assumed to be one source for ultra-fine particle emission. UFP release typically follows the flow path of the cooling air which may leave the printer casing at various points (e.g. the paper tray). This limits the usability of the commercial filter systems available because the released particles could leave the printer without passing through the filter. Chamber measurements with various filter systems retrofitted to a laser printer demonstrate different efficiencies of UFP reduction. Complementary experiments were carried out in an office room. Here the decay of the particle concentration after a print job was about ten times slower than in the test chamber. A toxicological assessment of the emitted particles requires that their chemical composition be known. Due to the low mass of the released UFPs chemical analysis needs a prior enrichment on a feasible media. Experiments using electrostatic precipitation showed a flame retardant (tri-xylyl phosphate) whose concentration on the media was dependent on the number of pages printed. Whether this compound was particle-bound could not be determined.

Organic Indoor Air Pollutants

Organic indoor air pollutants , Organic indoor air pollutants , کتابخانه دیجیتال جندی شاپور اهواز

Transdermal uptake of diethyl phthalate and di(n-butyl) phthalate directly from air: Experimental verification

Background Fundamental considerations indicate that, for certain phthalate esters, dermal absorption from air is an uptake pathway that is comparable to or greater than inhalation. Yet this pathway has not been experimentally evaluated and has been largely overlooked when assessing uptake of phthalate esters. Objectives This study investigated transdermal uptake, directly from air, of diethyl phthalate (DEP) and di(n-butyl) phthalate (DnBP) in humans. Methods In a series of experiments, six human participants were exposed for 6 hr in a chamber containing deliberately elevated air concentrations of DEP and DnBP. The participants either wore a hood and breathed air with phthalate concentrations substantially below those in the chamber or did not wear a hood and breathed chamber air. All urinations were collected from initiation of exposure until 54 hr later. Metabolites of DEP and DnBP were measured in these samples and extrapolated to parent phthalate intakes, corrected for background and hood air exposures. Results For DEP, the median dermal uptake directly from air was 4.0 μg/(μg/m3 in air) compared with an inhalation intake of 3.8 μg/(μg/m3 in air). For DnBP, the median dermal uptake from air was 3.1 μg/(μg/m3 in air) compared with an inhalation intake of 3.9 μg/(μg/m3 in air). Conclusions This study shows that dermal uptake directly from air can be a meaningful exposure pathway for DEP and DnBP. For other semivolatile organic compounds (SVOCs) whose molecular weight and lipid/air partition coefficient are in the appropriate range, direct absorption from air is also anticipated to be significant. Citation Weschler CJ, Bekö G, Koch HM, Salthammer T, Schripp T, Toftum J, Clausen G. 2015. Transdermal uptake of diethyl phthalate and di(n-butyl) phthalate directly from air: experimental verification. Environ Health Perspect 123:928–934; http://dx.doi.org/10.1289/ehp.1409151

Interaction of volatile organic compounds with indoor materials -a small-scale screening method

Abstract Indoor air pollution caused by volatile organic compounds (VOCs) may affect the health and well-being of inhabitants. Uptake and release of these compounds by and from indoor materials alter their concentrations in indoor air: uptake will lower peak concentrations, whereas subsequent (slow) release at lower concentration levels will prolong the presence of VOCs in indoor air. An experimental set-up has been implemented where indoor materials are placed as a “membrane” separating two air compartments. Both compartments – consisting of Field and Laboratory Emission Cells FLECs – are constantly flushed with air, one air stream containing a mixture of 20 VOCs, and concentrations in both compartments are measured after 1 h. Ten materials usually covering extensive surfaces indoors were consecutively exposed to the vapour mixture at concentration levels typically found in indoor environments. Under the chosen experimental conditions, five of these materials exhibited a permeability high enough that VOCs could be detected on the other side. Mass transport of VOCs into and through indoor materials has therefore been confirmed by experiment. The set-up allows for a quick screening of indoor materials with respect to their sorption capacity and permeability.

Critical evaluation of approaches in setting indoor air quality guidelines and reference values

The importance of good indoor air quality for the health of the individual was recognized as long as 150 years ago and that period also saw recommendations, which essentially related to questions of ventilation and carbon dioxide. The first evaluation standards for organic and inorganic substances were laid down in the 1970s, often on an empirical basis. It was in the mid-1980s of the 20th century that a shift occurred towards systematically evaluating the results of indoor air measurements, carrying out representative environmental surveys and deriving guideline values and reference values on the basis of toxicological, epidemiological and statistical criteria. Generally speaking the indoor environment is an area which can only be assessed with difficulty since its occupants are in most cases exposed to mixtures of substances and there can be great local and temporal variations in the substance spectrum. Data are available today for a large number of substances and this makes it possible, with the aid of statistically derived reference values and toxicologically based guideline values, to make useful recommendations regarding good indoor air quality. Nevertheless, it is still difficult to evaluate reactive compounds and reaction products. What is disadvantageous, however, is the fact that different guideline values may be published for one and the same substance, whose justification and area of application are often not transparent. A guideline or reference value can only be regarded as rational when necessary and when a strategy for its verification is available.

Experimental setup and analytical methods for the non-invasive determination of volatile organic compounds, formaldehyde and NOx in exhaled human breath.

Different analytical devices were tested and evaluated for their suitability of breath gas analysis by examining the physiological parameters and chemical substances in the exhaled breath of ten healthy probands during light cycling in dependence of methanol-rich nutrition. The probands exercised under normal breathing conditions on a bicycle ergometer. Breath air was exhaled into a glass cylinder and collected under steady-state conditions. Non-invasively measured parameters were pulse rate, breath frequency, temperature, relative humidity, NO(x), total volatile organic compounds (TVOC(PAS)), carbon dioxide (CO(2)), formaldehyde, methanol, acetaldehyde, acetone, isoprene and volatile organic compounds (VOCs). Methanol rich food and beverages strongly influenced the concentration of methanol and other organic substances in human breath. On the other hand, nutrition and smoking had no clear effect on the physical conditions of the probands. The proton transfer reaction mass spectrometry (PTR-MS) method was found to be very suitable for the analysis of breath gas but the m/z 31, if assigned to formaldehyde, is sensitive to interferences. The time vs. concentration curves of nitric oxide showed sudden peaks up to 120ppb in most of the measurements. In one case a strong interference of the NO(x) signal was observed. The time resolved analysis of exhaled breath gas is of high capability and significance for different applications if reliable analytical techniques are used. Some compounds like nitric oxide (NO), methanol, different VOCs as well as sum parameters like TVOC(PAS) are especially suitable as markers. Formaldehyde, which is rapidly metabolized in the human body, could be measured reliably as a trace component by the acetylacetone (acac) method but not by PTR-MS.

Role of clothing in both accelerating and impeding dermal absorption of airborne SVOCs

To assess the influence of clothing on dermal uptake of semi-volatile organic compounds (SVOCs), we measured uptake of selected airborne phthalates for an individual wearing clean clothes or air-exposed clothes and compared these results with dermal uptake for bare-skinned individuals under otherwise identical experimental conditions. Using a breathing hood to isolate dermal from inhalation uptake, we measured urinary metabolites of diethylphthalate (DEP) and di-n-butylphthalate (DnBP) from an individual exposed to known concentrations of these compounds for 6 h in an experimental chamber. The individual wore either clean (fresh) cotton clothes or cotton clothes that had been exposed to the same chamber air concentrations for 9 days. For a 6-h exposure, the net amounts of DEP and DnBP absorbed when wearing fresh clothes were, respectively, 0.017 and 0.007 μg/kg/(μg/m3); for exposed clothes the results were 0.178 and 0.261 μg/kg/(μg/m3), respectively (values normalized by air concentration and body mass). When compared against the average results for bare-skinned participants, clean clothes were protective, whereas exposed clothes increased dermal uptake for DEP and DnBP by factors of 3.3 and 6.5, respectively. Even for non-occupational environments, wearing clothing that has adsorbed/absorbed indoor air pollutants can increase dermal uptake of SVOCs by substantial amounts relative to bare skin.

Comparison of analytical techniques for the determination of aldehydes in test chambers

The level of carbonyl compounds in indoor air is crucial due to possible health effects and the high prevalence of their potential sources. Therefore, selecting a convenient and rapid analytical technique for the reliable detection of carbonyl compound concentrations is important. The acetyl acetone (acac) method is a widely used standard procedure for detecting gaseous formaldehyde. For measuring formaldehyde along with other carbonyl compounds, the DNPH-method is commonly applied. The recommended procedure for measuring volatile organic compounds (VOCs) is sampling on Tenax TA, followed by thermal desorption and GC/MS analysis. In this study, different analytical techniques for the quantification of formaldehyde, pentanal, and hexanal are critically compared. It was found that the acac- and DNPH-method are in very good agreement for formaldehyde. In contrast, the DNPH-method significantly underestimates indoor air concentrations of the higher aldehydes in comparison to sampling on Tenax TA, although both methods are strongly correlated. The reported results are part of the EURIMA-WKI study on levels of indoor air pollutants resulting from construction, building materials and interior decoration.