Biological monitoring for exposure to volatile organic compounds (VOCs) (IUPAC Recommendations 2000)

2000 ◽  
Vol 72 (3) ◽  
pp. 385-436 ◽  
Author(s):  
R. Heinrich-Ramm ◽  
M. Jakubowski ◽  
B. Heinzow ◽  
J. Molin Christensen ◽  
E. Olsen ◽  
...  

This paper deals with the appropriate application of biological monitoring (BM) for exposure to volatile organic compounds (VOCs). Sampling guidelines, approved analytical procedures, quality control systems, detailed aspects for the interpretation of biomonitoring data, a compilation of international biological action values for VOC exposure at the workplace (e.g., BAT, BEI®), and state of the art reference values are outlined or referred to in this review for recommendation as guidelines for health professionals in occupational and environmental settings.VOCs are frequently encountered at the workplace, in daily routines and widely used consumer products. They cover a broad spectrum of chemical classes with different physicochemical and biological properties. Inhalation is a prominent route of exposure due to their volatility but many VOCs can quite readily be absorbed through the skin. BM allows assessment of the integrated exposure by different routes including inhalation and concomitant dermal and oral uptake—a helpful tool for relating exposure to body burden and possible health effects. Because of the different toxicological profiles of VOCs, no uniform approach for BM can be recommended. VOCs in blood and urinary VOC metabolites are most often applied for BM. Limit values for workplace exposure have been established for many VOCs. In this field, profound analytical methodology and extensive experience exist in numerous international scientific laboratories for reliable routine application. Contamination and loss of VOCs during specimen collection, storage and sample treatment, and applied calibration procedure are the most important uncertainties for analytical quantification of VOCs in blood. For interpretation of the analytical results appropriate time of sampling, according to toxicokinetics of the compound, is crucial due to VOC elimination with short but differing biological half-lives. Lifestyle factors (such as smoking habits, alcohol consumption, and dietary habits), workload, personal working habits, exposure to VOC mixtures and endogeous factors (as genetic polymorphism for VOC metabolizing enzymes, body mass) contribute to BM results and have to be considered in detail. Future analytical work should focus on the improvement of analytical methodology of VOC determination in body fluids at low-level environmental exposure and evaluation of corresponding reference intervals.

2012 ◽  
Vol 2012 ◽  
pp. 1-6 ◽  
Author(s):  
Luis Juan-Peiró ◽  
Anne Bernhammer ◽  
Agustin Pastor ◽  
Miguel de la Guardia

Passive samplers have been widely used for volatile organic compounds determination. Following the green chemistry tendency of the direct determination of adsorbed compounds in membrane-based devices through using head space direct chromatography analysis, this work has evaluated the use of Amberlite XAD-2, XAD-4, and XAD-16 adsorbents as a filling material for passive samplers. Direct analysis of the membranes by HS-GC-MS involves a solvent-free method avoiding any sample treatment. For exposed membranes, recoveries ranged from 10% to 203%, depending on the compound and adsorbent used. The limit of the detection values ranged from 1 to 140 ng per sampler. Acceptable precision and sensitivity levels were obtained for the XAD resins assayed.


2020 ◽  
Vol 19 (1) ◽  
pp. 43-56
Author(s):  
Veerapas Na Roi-et ◽  
◽  
Supawat Chaikasem ◽  

Emission of volatile organic compounds (VOCs) from photocopiers was investigated to assess the potential health impacts on inhalation exposure to VOCs. VOCs samples were collected during working hours using SKC VOCs 575 series passive sample. Twenty-one quantified VOCs were measured and analyzed by GC-MS/MS. The results showed that the total VOCs concentration emitted in the photocopy centers A and B were 2.29×104 and 2.32×104 µg/m3, respectively. The highest detected chemical was trans-1,2-Dichloroethene at about 2.18×104 (photocopy center A) and 2.15×104 µg/m3 (photocopy center B (The results reveal that the non-carcinogenic risk for inhalation exposure to m-Xylene, p-Xylene, and trans-1,2-Dichloroethene were in the range 0.94-1.53 and 1.19-1.79 and 51.54-52.23, respectively, resulting in the hazard index (HI) of non-carcinogenic VOCs in total being greater than 1.0. This indicated that the cumulative effects of inhalation exposure to VOCs at low concentrations should be of concern, even though it does not exceed the occupational exposure limits and Threshold Limit Values-Time Weighted Average for the mixtures (TLV-TWAmix). Plants display a greener solution to reduce indoor air pollution. The bio-concentration levels of total VOCs in Epipremnum aureum were noted as 74.71 to 174.42, signifying that E. aureum is effective for removal of VOCs naturally and sustainably.


2014 ◽  
Vol 77 (22-24) ◽  
pp. 1502-1521 ◽  
Author(s):  
Seong Kwang Lim ◽  
Han Seung Shin ◽  
Kyung Sil Yoon ◽  
Seung Jun Kwack ◽  
Yoon Mi Um ◽  
...  

Sensors ◽  
2021 ◽  
Vol 21 (16) ◽  
pp. 5659
Author(s):  
Michael S. Breen ◽  
Vlad Isakov ◽  
Steven Prince ◽  
Kennedy McGuinness ◽  
Peter P. Egeghy ◽  
...  

Personal exposure to volatile organic compounds (VOCs) from indoor sources including consumer products is an understudied public health concern. To develop and evaluate methods for monitoring personal VOC exposures, we performed a pilot study and examined time-resolved sensor-based measurements of geocoded total VOC (TVOC) exposures across individuals and microenvironments (MEs). We integrated continuous (1 min) data from a personal TVOC sensor and a global positioning system (GPS) logger, with a GPS-based ME classification model, to determine TVOC exposures in four MEs, including indoors at home (Home-In), indoors at other buildings (Other-In), inside vehicles (In-Vehicle), and outdoors (Out), across 45 participant-days for five participants. To help identify places with large emission sources, we identified high-exposure events (HEEs; TVOC > 500 ppb) using geocoded TVOC time-course data overlaid on Google Earth maps. Across the 45 participant-days, the MEs ranked from highest to lowest median TVOC were: Home-In (165 ppb), Other-In (86 ppb), In-Vehicle (52 ppb), and Out (46 ppb). For the two participants living in single-family houses with attached garages, the median exposures for Home-In were substantially higher (209, 416 ppb) than the three participant homes without attached garages: one living in a single-family house (129 ppb), and two living in apartments (38, 60 ppb). The daily average Home-In exposures exceeded the estimated Leadership in Energy and Environmental Design (LEED) building guideline of 108 ppb for 60% of the participant-days. We identified 94 HEEs across all participant-days, and 67% of the corresponding peak levels exceeded 1000 ppb. The MEs ranked from the highest to the lowest number of HEEs were: Home-In (60), Other-In (13), In-Vehicle (12), and Out (9). For Other-In and Out, most HEEs occurred indoors at fast food restaurants and retail stores, and outdoors in parking lots, respectively. For Home-In HEEs, the median TVOC emission and removal rates were 5.4 g h−1 and 1.1 h−1, respectively. Our study demonstrates the ability to determine individual sensor-based time-resolved TVOC exposures in different MEs, in support of identifying potential sources and exposure factors that can inform exposure mitigation strategies.


2018 ◽  
Vol 8 (18) ◽  
Author(s):  
Ajoke F. Idayat Apanpa-Qasim ◽  
Adebola A. Adeyi

Background. Consumer products such as paints are a potentially significant source of volatile organic compounds (VOCs) and oxygenated VOCs. Paints for construction and household use have been rapidly changing from oil-based to water-based paints and are one of the commonly identified sources of oxygenated VOCs in indoor environments. Objectives. Four different anti-freezing agents were identified and analyzed in 174 waterbased paint samples, purchased from popular paint markets in two metropolitan cities in Nigeria, Lagos and Ibadan. Methods. Paint samples were solvent extracted using acetonitrile and milli-Q water. Antifreezing agents in the extracts were identified and quantified using gas chromatography (GC)-mass spectrometry and a GC-flame ionization detector, respectively. Discussion. Four different anti-freezing agents were identified in the samples, ethylene glycol, diethylene glycol, triethylene glycol and propylene glycol. Their levels ranged from 1,000-1,980 ppm, diethylene glycol; 1,000–3,900 ppm, triethylene glycol; 1,090–2,510 ppm, propylene glycol and 1,350–2,710 ppm, ethylene glycol. Levels of anti-freezing agents in all of the paint samples were above the permissible limits of the European Union for VOCs in paints of 500 ppm. Results of multivariate statistical analyses clearly showed that triethylene glycol was the most commonly used anti-freezing agent in paints despite its numerous harmful health effects. Conclusions. We concluded that water-based paints marketed in Nigeria contain high concentrations of anti-freezing agents, which have harmful environmental and human health effects, especially to sensitive individuals such as children. Competing Interests. The authors declare no competing financial interests.


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