Polyurethane Foam Disks Research Articles

Characterizing PUF disk passive air samplers for alkyl-substituted PAHs: Measured and modelled PUF-AIR partition coefficients with COSMO-RS.

Isomers of alkyl-substituted polycyclic aromatic hydrocarbons (PAHs) and dibenzothiophenes are modelled with COSMO-RS theory to determine the effectiveness and accuracy of this approach for estimation of isomer-specific partition coefficients between air and polyurethane foam (PUF), i.e., KPUF-AIR. Isomer-specific equilibrium partitioning coefficients for a series of 23 unsubstituted and isomeric alkyl-substituted PAHs and dibenzothiophenes were measured at 22 °C. This data was used to determine the accuracy of estimated values using COSMO-RS, which is isomer specific, and the Global Atmospheric Passive Sampling (GAPS) template approach, which treats all alkyl-substitutions as a single species of a given side-chain carbon number. A recently developed oligomer-based model for PUF was employed, which consisted of a 1:1 condensed pair of 2,4-toluene-diisocyanide and glycerol. The COSMO-RS approach resulted in a significant reduction in the RMS error associated with simple PAHs and dibenzothiophene compared with the GAPS template approach. When used with alkylated PAHs and dibenzothiophenes grouped into carbon-number categories, the GAPS template approach gave lower RMS error (0.72) compared to the COSMO-RS result (0.87) when the latter estimates were averaged within the carbon-number-based categories. When the isomer-specific experimental results were used, the COSMO-RS approach resulted in a 21% reduction in RMS error with respect to the GAPS template approach, with a 0.57 RMS error for all alkylated PAHs and dibenzothiophenes studied. The results demonstrate that COSMO-RS theory is effective in generating isomer-specific PUF-air partition coefficients, supporting the application of PUF-based passive samplers for monitoring and research studies of polycyclic aromatic compounds (PACs) in air.

Antimicrobial Activity of a Novel Vascular Access Film Dressing Containing Chlorhexidine Gluconate

BackgroundCovering insertion sites with chlorhexidine impregnated dressings has been proven to be clinically effective in reducing catheter related blood stream infections (CR-BSI). Two chlorhexidine gluconate (CHG)-impregnated dressings are commercially available, a polyurethane foam disk and a film dressing containing a chlorhexidine gluconate-impregnated gel pad. While both have demonstrated efficacy in clinical settings, the major drawback of high cost and impaired IV insertion site visibility limits their usage. A new, simple film dressing containing CHG within its adhesive layer is now available. The objective of this study was to test the in vitro antimicrobial efficacy of the new dressing in comparison to the CHG-impregnated gel dressing.MethodsQuantitative aliquots of suspensions (concentration of 1.0x106 to 5.0x106 cfu/sample) of clinically relevant challenge organisms (Staphylococcus species, gram-negative bacilli, Candida albicans) were incubated in contact with the new CHG-containing film dressing, a placebo version of the same (negative control) and the commercially available CHG-impregnated gel dressing (positive control). Serial dilutions of the surviving organisms were quantified using the pour plate after 1, 3, 5, and 7 days of incubation in order to calculate an antimicrobial log10 reduction for each organism/dressing combination at each point in time.ResultsThe new CHG-containing film dressing delivered greater than 5.0 log10 reduction throughout the 7 days on all aerobic gram-negative bacilli and Staphylococcus species tested. As of day 1 the CHG-containing film dressing provided greater than 5.0 log10 reduction on Candida albicans. There were no statistically significant differences in the log10 reduction between the two dressings tested.ConclusionThe new CHG-containing film dressing was found to be as effective as the chlorhexidine gluconate-impregnated gel dressing on clinically relevant microbes.

Using air, soil and vegetation to assess the environmental behaviour of siloxanes.

This study aimed to contribute to the enhancement of the knowledge of levels, trends and behaviour of eight siloxanes (four linear and four cyclic) in the environment. Adding to the prioritised scrutiny of the incidence in the atmosphere through passive samplers (sorbent-impregnated polyurethane foam disks--SIPs), the sampling of pine needles and soil was also performed, thus closing the circle of atmospheric exposure in the areas of study. Two sampling campaigns (one in summer and one in winter) were done in a total of eight sampling points in the Portuguese territory, which covered a wide range of human presence and land uses (urban, industrial, remote and beach areas). By adopting a "green" approach in terms of analytical methods, namely reducing the clean-up steps for the passive air samples and using the quick, easy, cheap, effective, rugged and safe (QuEChERS) technology for soils and pine needles, the results showed total concentration of siloxanes between 5 and 70 ng g(-1) (dry weight) for soils and from 2 to 118 ng g(-1) (dry weight (dw)) for pine needles, with no clear seasonal trend. For SIPs, the levels varied from 0.6 to 7.8 ng m(-3) and were higher in summer than in winter in all sites. Overall, the cyclic siloxanes were found in much higher concentrations, with D5 and D6 being the most predominant in a great majority of cases. Also, the urban and industrial areas had the highest incidence, suggesting a strong anthropogenic fingerprint, in line with their main uses.

Sources and potential health risk of gas phase PAHs in Hexi Corridor, Northwest China.

Gas phase polycyclic aromatic hydrocarbons (PAHs) in Hexi Corridor, Northwest China were determined during heating and non-heating seasons, respectively, using passive air samplers. Polyurethane foam (PUF) disks were chosen as the sampling medium. Fifteen PAHs out of the 16 PAHs classified by the United States Environmental Protection Agency (U.S. EPA) were detected in this field sampling investigation. The atmospheric levels of sampled PAHs were higher at urban sites than that at rural sites among 14 sampling sites and increased during heating season. The highest concentration (11.34 ng m(-3)) was observed in Lanzhou during the heating season, the capital and largest industrial city of Gansu Province. PAH contamination in air was dominated by three aromatic ring congeners. Possible sources of PAHs were apportioned using PAH species ratios and the principle component analysis (PCA) combined with a multiple linear regression (MLR) method. Fossil fuel consumption was identified to be the predominant source of PAHs over Hexi Corridor, accounting for 43 % of the concentration of total (15) PAHs. Backward and forward trajectory and cluster analysis were also carried out to identify potential origins of PAHs monitored at several urban and rural sites. Lung cancer risk of local residents to gas phase PAHs via inhalation exposure throughout the province was found to be around a critical value of the lung cancer risk level at 10(-6) recommended by the U.S. EPA risk assessment guideline.

Spatial and seasonal variations of atmospheric organochlorine pesticides along the plain-mountain transect in central China: Regional source vs. long-range transport and air–soil exchange

Polyurethane foam (PUF) disk passive air samplers (PAS) were deployed to measure spatiality and seasonality of atmospheric OCPs in Jianghan Plain (JHP) and Western Hubei Mountain (WHM), to make a preliminary explorative study of the source–sink relationship of organochlorine pesticides (OCPs) and their association with the monsoon. The concentrations of individual OCPs in the JHP were generally higher than those in the WHM. Significantly high levels of DDTs and Endosulfan were found in the spring and summer, HCB was found in autumn and winter, and HCHs displayed uniform distributions. Compared with the levels of 2005, a significant decrease of atmospheric HCHs, DDTs and HCB was observed, whereas an increase in Endosulfan was observed. The air–soil equilibrium status of OCPs suggested that Dajiuhu (DJH) soils are likely to be a sink for OCPs, and JHP soils are acting as the emitter, contaminating the atmosphere at certain monitoring stations. Backward air trajectory analysis demonstrated that the seasonal fluctuation of atmospheric DDTs, HCB and Endosulfan at the DJH site were closely associated with the variations of the East Asian monsoon.

Stability of polycyclic aromatic compounds in polyurethane foam-type passive air samplers upon O3 exposure

Stability of polycyclic aromatic compounds (PACs) in polyurethane foam (PUF) disks upon O3 exposure was studied in a flow tube. A wide range of PACs was evaluated by spiking PUF disks with PACs and exposing to O3 at concentrations that were equivalent to two months exposure, a typical deployment period for these passive air samplers. Ambient concentrations of O3 (∼50 ppb) at 0% and 50% relative humidity (RH) were applied. At 0% RH, 23 of 68 PACs yielded more than 50% loss after exposure. The mean percent loss was 30% with perylene and 9,10-dimethylanthracene the most reactive polycyclic aromatic hydrocarbons (PAHs) and alkylated PAHs, respectively. At 50% RH, 77% of the studied PACs was stable upon O3 exposure (PACexposed/PACunexposed > 0.7). The mean percent loss was 17% and only 7 of 68 PACs yielded greater than 50% loss. In general, the reactivity of most of the PACs decreased at higher RH, except for the reactive PAHs (acenaphthylene, 2,3-dimethylanthracene, 9,10-dimethylanthracene, dibenzothiophene, and 2-methyldibenzothiophene) which demonstrated lower RH dependence. The experimental conditions in this study represent a worst case scenario for the stability of PACs sorbed to PUF. In reality, the sampling of PACs in ambient air represents an ‘aged’ component of PACs where the most reactive species have already partially been removed. Also, PACs in ambient air will be associated with the particle phase to varying extents that will help to enhance their stability. Therefore, under regular operating conditions, over a 2-month exposure, we expect a minimal error in the measurement of total concentration of PACs in air using the PUF disk passive sampler.

Calibration of two passive air samplers for monitoring phthalates and brominated flame-retardants in indoor air

Two passive air samplers (PAS), polyurethane foam (PUF) disks and Sorbent Impregnated PUF (SIP) disks, were characterized for uptake of phthalates and brominated flame-retardants (BFRs) indoors using fully and partially sheltered housings. Based on calibration against an active low-volume air sampler for gas- and particle-phase compounds, we recommend generic sampling rates of 3.5±0.9 and 1.0±0.4m3/day for partially and fully sheltered housing, respectively, which applies to gas-phase phthalates and BFRs as well as particle-phase DEHP (the later for the partially sheltered PAS). For phthalates, partially sheltered SIPs are recommended. Further, we recommend the use of partially sheltered PAS indoors and a deployment period of one month. The sampling rate for the partially sheltered PUF and SIP of 3.5±0.9m3/day is indistinguishable from that reported for fully sheltered PAS deployed outdoors, indicating the role of the housing outdoors to minimize the effect of variable wind velocities on chemical uptake, versus the partially sheltered PAS deployed indoors to maximize chemical uptake where air flow rates are low.

Assessing Polycyclic Aromatic Hydrocarbons (PAHs) using passive air sampling in the atmosphere of one of the most wood-smoke-polluted cities in Chile: The case study of Temuco

This study addresses human health concerns in the city of Temuco that are attributed to wood smoke and related pollutants associated with wood burning activities that are prevalent in Temuco. Polycyclic Aromatic Hydrocarbons (PAHs) were measured in air across urban and rural sites over three seasons in Temuco using polyurethane foam (PUF) disk passive air samplers (PUF-PAS). Concentrations of ΣPAHs (15 congeners) in air ranged from BDL to ∼70ngm−3 and were highest during the winter season, which is attributed to emissions from residential heating by wood combustion. The results for all three seasons showed that the PAH plume was widespread across all sites including rural sites on the outskirts of Temuco. Some interesting variations were observed between seasons in the composition of PAHs, which were attributed to differences in seasonal point sources. A comparison of the PAH composition in the passive samples with active samples (gas+particle phase) from the same site revealed similar congener profiles. Overall, the study demonstrated that the PUF disk passive air sampler provides a simple approach for measuring PAHs in air and for tracking effectiveness of pollution control measures in urban areas in order to improve public health.

Assessing levels and seasonal variations of current-use pesticides (CUPs) in the Tuscan atmosphere, Italy, using polyurethane foam disks (PUF) passive air samplers

Polyurethane foam disks (PUF) passive air samplers (PAS) were deployed over 4 sampling periods of 3–5-months (≥ 1 year) at ten urban and rural locations throughout the Tuscany Region. The purpose was to assess the occurrence and seasonal variations of ten current-use pesticides (CUPs). PUF disk extracts were analyzed using GC–MS. The organophosphates insecticides; chlorpyrifos (3–580 pg m−3) and chlorpyrifos-methyl (below detection limit – to 570 pg m−3) presented the highest levels in air, and showed seasonal fluctuation coinciding with the growing seasons. The relative proportion urban/(urban + rural) ranged from 0.4 to 0.7 showing no differences between urban and rural concentrations. Air back trajectories analysis showed air masses passing over agricultural fields and potentially enhancing the drift of pesticides into the urban sites. This study represents the first information regarding CUPs in the atmosphere of Tuscany region using PAS-PUF disk.

Variations of Flame Retardant, Polycyclic Aromatic Hydrocarbon, and Pesticide Concentrations in Chicago's Atmosphere Measured using Passive Sampling.

Atmospheric concentrations of flame retardants, polycyclic aromatic hydrocarbons, and pesticides were measured using passive air samplers equipped with polyurethane foam disks to find spatial information in and around Chicago, Illinois. Samplers were deployed around the greater Chicago area for intervals of 6 weeks from 2012 to 2013 (inclusive). Volumes were calculated using passive sampling theory and were based on meteorology and the compounds' octanol-air partition coefficients. Geometric mean concentrations of total polybrominated diphenyl ethers ranged from 11 to 150 pg/m3, and tributyl phosphate, tris(2-chloroethyl)phosphate, tris(1-chloro-2-propyl)phosphate, and triphenyl phosphate concentrations were in the ranges of 54-290, 32-340, 130-580, and 170-580 pg/m3, respectively. The summed concentrations of 16 PAHs ranged from 8700 to 52,000 pg/m3 over the sampling area, and DDT, chlordane, and endosulfan concentrations were in the ranges of 2.7-9.9, 8.2-66, and 16-85 pg/m3, respectively. Sampling sites were split into two groups depending on their distances from the Illinois Institute of Technology campus in Chicago. With a few exceptions, the concentrations of most compound groups in the city's center were the same or slightly higher than those measured >45 km away. The data also showed that the concentrations measured with a passive atmospheric sampling system are in good agreement with those measured with an active, high-volume, sampling system. Given that the sampling times are different (passive, 43 days; active, 1 day), and that both of these measured concentrations cover about 5 orders of magnitude, the agreement between these passive and active sampling methods is excellent.

Assessing polychlorinated dibenzo-p-dioxins and polychlorinated dibenzofurans in air across Latin American countries using polyurethane foam disk passive air samplers.

A passive air sampling network has been established to investigate polychlorinated dibenzo-p-dioxins (PCDDs) and polychlorinated dibenzofurans (PCDFs) at Global Atmospheric Passive Sampling (GAPS) sites and six additional sites in the Group of Latin American and Caribbean Countries (GRULAC) region. The air sampling network covers background, agricultural, rural, and urban sites. Samples have been collected over four consecutive periods of 6 months, which started in January 2011 [period 1 (January to June 2011), period 2 (July to December 2011), period 3 (January to June 2012), and period 4 (July 2012 to January 2013)]. Results show that (i) the GAPS passive samplers (PUF disk type) and analytical methodology are adequate for measuring PCDD/F burdens in air and (ii) PCDD/F concentrations in air across the GRULAC region are widely variable by almost 2 orders of magnitude. The highest concentrations in air of Σ4-8PCDD/Fs were found at the urban site São Luis (Brazil, UR) (i.e., 2560 fg/m3) followed by the sites in São Paulo (Brazil, UR), Mendoza (Argentina, RU), and Sonora (Mexico, AG) with values of 1690, 1660, and 1610 fg/m3, respectively. Very low concentrations of PCDD/Fs in air were observed at the background site Tapanti (Costa Rica, BA), 10.8 fg/m3. This variability is attributed to differences in site characteristics and potential local/regional sources as well as meteorological influences. The measurements of PCDD/Fs in air agree well with model-predicted concentrations performed using the Global EMEP Multimedia Modeling System (GLEMOS) and emission scenario constructed on the basis of the UNEP Stockholm Convention inventory of dioxin and furan emissions.

Cadmium removal by Anabaena sp. ATCC 33047 immobilized in polyurethane foam

The nitrogen-fixing cyanobacterium Anabaena sp. ATCC 33047, which generates substantial amounts of exopolysaccharide, was immobilized by entrapment within the reticulate network of polyurethane foam discs. The immobilized Anabaena sp. system has been investigated as a potential biosorbent for the removal of cadmium from aqueous solutions. The results showed that it was a highly fast process, with 80 % of the adsorption taking place in the first 10 min, reaching full equilibrium in about 50 min. Data analysis indicated that the behaviour of the system accurately fits to a monolayer adsorption model (Langmuir isotherm). The maximal biosorption capacity determined for the immobilized Anabaena sp. system was as high as 162 mg Cd (II) per gram dry biomass. The outstanding properties established for immobilized Anabaena sp. in polyurethane foam underline the relevance of such a system as an alternative to current treatments of variety effluents or wastewater contaminated with cadmium.

First results from the oil sands passive air monitoring network for polycyclic aromatic compounds.

Results are reported from an ongoing passive air monitoring study for polycyclic aromatic compounds (PACs) in the Athabasca oil sands region in Alberta, Canada. Polyurethane foam (PUF) disk passive air samplers were deployed for consecutive 2-month periods from November 2010 to June 2012 at 17 sites. Samples were analyzed for polycyclic aromatic hydrocarbons (PAHs), alkylated PAHs, dibenzothiophene and its alkylated derivatives (DBTs). Relative to parent PAHs, alkylated PAHs and DBTs are enriched in bitumen and therefore considered to be petrogenic markers. Concentrations in air were in the range 0.03-210 ng/m(3), 0.15-230 ng/m(3) and 0.01-61 ng/m(3) for ∑PAHs, ∑alkylated PAHs and ΣDBTs, respectively. An exponential decline of the PAC concentrations in air with distance from mining areas and related petrogenic sources was observed. The most significant exponential declines were for the alkylated PAHs and DBTs and attributed to their association with mining-related emissions and near-source deposition, due to their lower volatility and greater association with depositing particles. Seasonal trends in concentrations in air for PACs were not observed for any of the compound classes. However, a forest fire episode during April to July 2011 resulted in greatly elevated PAH levels at all passive sampling locations. Alkylated PAHs and DBTs were not elevated during the forest fire period, supporting their association with petrogenic sources. Based on the results of this study, an "Athabasca PAC profile" is proposed as a potential source marker for the oil sands region. The profile is characterized by ∑PAHs/∑Alkylated PAHs = ∼0.2 and ∑PAHs/∑DBTs = ∼5.

Temporal variations of cyclic and linear volatile methylsiloxanes in the atmosphere using passive samplers and high-volume air samplers.

Cyclic and linear volatile methylsiloxanes (cVMSs and lVMSs, respectively) were measured in ambient air over a period of over one year in Toronto, Canada. Air samples were collected using passive air samplers (PAS) consisting of sorbent-impregnated polyurethane foam (SIP) disks in parallel with high volume active air samplers (HV-AAS). The average difference between the SIP-PAS derived concentrations in air for the individual VMSs and those measured using HV-AAS was within a factor of 2. The air concentrations (HV-AAS) ranged 22-351 ng m(-3) and 1.3-15 ng m(-3) for ΣcVMSs (D3, D4, D5, D6) and ΣlVMSs (L3, L4, L5), respectively, with decamethylcyclopentasiloxane (D5) as the dominant compound (∼75% of the ΣVMSs). Air masses arriving from north to northwest (i.e., less populated areas) were significantly less contaminated with VMSs compared to air arriving from the south that are impacted by major urban and industrial areas in Canada and the U.S. (p < 0.05). In addition, air concentrations of ΣcVMSs were lower during major snowfall events (on average, 73 ng m(-3)) in comparison to the other sampling periods (121 ng m(-3)). Ambient temperature had a small influence on the seasonal trend of VMS concentrations in air, except for dodecamethylcyclohexasiloxane (D6), which was positively correlated with the ambient temperature (p < 0.001).

Persistent Organic Pollutants (POPs) in the atmosphere of agricultural and urban areas in the Province of Buenos Aires in Argentina using PUF disk passive air samplers

Passive air samplers consisting of polyurethane foam (PUF) disks were deployed in a network of eight sites across agricultural and urban areas in the Province of Buenos Aires in Argentina to assess levels of polychlorinated biphenyls (PCBs) and organochlorine pesticides (OCPs) during two sampling periods in 2006 and 2007. Concentrations (pg m−3) of PCBs in air ranged from BDL to 360, with an average at urban sites of Bahia Blanca (200±130) about one order of magnitude higher than at agricultural sites in the Province of Buenos Aires (20±20). Endosulfan exhibited the highest concentrations of all the chemicals investigated with a maximum of 16 000pg m−3 in the agricultural area. The remaining OCPs had lower levels (pg m−3) in the following ranges: ΣHCH (α−+γ− hexachlorocyclohexane) from 1 to 50, HEPT (heptachlor) and HEPX (heptachlor epoxide) from BDL to 20, chlordanes (Σtrans–chlordane, cis–chlordane and trans–nonachlor) from 1 to 40, dieldrin from BDL to 30, and p,p′–DDE (the only isomer of DDT that was detected) from BDL to 20. Concentrations of OCPs in air were highest at Bahia Blanca city and generally higher during the warmer sampling period. This study is one of the first investigations of the POPs composition in ambient air in the Province Buenos Aires of Argentina. The results support the Global Monitoring Plan of the Stockholm Convention on POPs and specifically, the need for air data to contribute to the regional report of the GRULAC (GRoUp of Latin American and Caribbean countries) region.

Air concentrations of currently used herbicides and legacy compounds in the Canadian prairies, subarctic, and arctic

Passive air samplers were installed in the summers of 2005 and 2007 for 90 days at four locations in the agricultural region of the Canadian Prairies and at five locations in the Canadian Subarctic and Arctic. The presence and masses of ten currently used herbicides and three legacy compounds in the polyurethane foam disks were quantified. Herbicides 2,4-D, bromoxynil and MCPA were detected at all locations in the Canadian Prairies and in both years because these herbicides are widely applied to control broadleaf weeds in cereal crops that are an integral part of Prairie agricultural production systems. MCPA was also detected at one location in the Arctic in 2007. The detection of the other seven herbicides in the 2 years combined ranged from no detections (atrazine only) to five detections for the relatively volatile herbicides trifluralin and triallate. Triallate was the only other herbicide detected in the Arctic (2005). Legacy compounds were either not detected (alachlor) or at levels near their detection level (γ-HCH and α-HCH). γ-HCH and α-HCH were more frequently detected in 2005 than in 2007 indicating that their concentrations in Canadian air have decreased over time. γ-HCH, widely used as an insecticide in Prairie oilseed production until 2002, was detected at larger concentrations in the Canadian Prairies than in the Subarctic and Arctic. α-HCH, a manufacturing by-product in technical HCH prior to 1971 in Canada, was not detected in the Canadian Prairies but was at detectable levels in the Subarctic and Arctic as the Arctic Ocean is reported to be a major source of α-HCH to the atmosphere. We conclude that some of the most widely used herbicides in Canadian agriculture today are commonly present in the air in regions where they are applied and that a portion of these herbicides may be traveling as parent molecules to the Canadian Arctic. To the authors’ knowledge, this is the first evidence of the presence of MCPA and triallate in Arctic air samples, perhaps because previous research has seldomly monitored for currently used herbicides in this region.

Characterization of urban pollution in two cities of the Puglia region in Southern Italy using field measurements and air quality (AQ) model approach

Passive air sampling (PAS) consisting of polyurethane foam (PUF) disks were deployed simultaneously over four periods of 2–5 months at four locations in urban and sub–urban sites of Bari and San Vito Taranto in Southern Italy. The purpose of the study was to characterize the urban pollution for two groups of semi volatile organic compounds (SVOCs), polychlorinated biphenyls (PCBs) and polycyclic aromatic hydrocarbons (PAHs), by using two different approaches consisting of PAS–PUF and air quality models (Flexible Air quality Regional Model, FARM). The concentrations in the air ranged from 20 to 200pg m−3 for PCBs and from 5 to 48ng m−3 for PAHs with the highest concentrations being detected at Bari center. PCB composition was dominated by the 3–Cl congeners (periods 1 and 2) and by 5–Cl (periods 3 and 4). PCB–28 and –37 were the most abundant congeners during the four periods. The PAHs profile was dominated by the 3–ring (70±6)%, with phenanthrene alone accounting for (49±2)%. On a seasonal basis opposite patterns were observed for PCBs and PAHs showing high PCB concentrations during the warm periods, period 3: summer and 2: spring, while PAHs were found during cool periods, period 4: autumn, and 1: winter. The results obtained from the application of the FARM model, during 2010, and limited to period 4 in this study, showed similar estimated levels for PCBs indicating a good performance for PCB modeled concentrations whilst for benzo[b]fluoranthene (B[b]F) the results showed a less better agreement. This study represents one of the few efforts at characterizing PCBs and PAHs compositions in ambient air in southern Italy and also represents one of the preliminary attempts at using PAS–PUF to give more insight into a modeling prediction in Italy. These results also provide useful information for the future development of the FARM model.

Outdoor passive air monitoring of semi volatile organic compounds (SVOCs): a critical evaluation of performance and limitations of polyurethane foam (PUF) disks

The most commonly used passive air sampler (PAS) (i.e. polyurethane foam (PUF) disk) is cheap, versatile, and capable of accumulating compounds present both in gas and particle phases. Its performance for particle associated compounds is however disputable. In this study, twelve sets of triplicate PUF-PAS were deployed outdoors for exposure periods of 1-12 weeks together with continuously operated active samplers, to characterize sampling efficiency and derive sampling rates (RS) for compounds belonging to 7 SVOC classes (including particle associated compounds). PUF-PAS efficiently and consistently sampled polychlorinated biphenyls (PCBs), organochlorine pesticides (OCPs), polycyclic aromatic hydrocarbons (PAHs), and eight novel brominated flame retardant (nBFR) compounds. Low accuracy and lack of sensitivity was observed for most polychlorinated dibenzo-p-dioxins/furans PCDD/Fs and polybrominated diphenyl ethers (PBDEs) (under the conditions of this study), with the exception of some congeners which may be used as qualitative markers for their respective classes. Application of compound specific RS was found crucial for all compounds except PCBs. Sampling efficiency of the particle associated compounds was often low.

A Case Study on the Long-Term Influence of Historical Intensive Usage of Organochlorine Pesticides on Current Ambient Air

Polyurethane foam disk passive air sampling was performed to investigate the levels and spatial distributions of organochlorine pesticides (OCPs) in the atmosphere of a typical city (Tangshan) in China where unparalleled amounts of OCPs including dichlorodiphenyltrichloroethane (DDT) and hexachlorocyclohexane (HCH) were used for sanitary purposes following the 1976 Tangshan Earthquake. This study aimed to investigate the long-term influence of historical intensive usage of OCPs during the earthquake on the current ambient air levels. Sampling was performed at seven sites in Tangshan between July and October 2010. The levels of Sigma DDTs and Sigma HCHs were relatively high, with concentrations ranging from 79-254 pg/m(3) and 117-176 pg/m(3), respectively. The concentration of hexachlorobenzene (HCB) was 69-89 pg/m(3). Technical DDTs and HCHs were sprayed for preventing epidemics mainly in the southern region of Tangshan in 1976. In this study, high levels of DDTs and HCHs were found in the southern region, and levels decreased considerably to the north. Unlike DDTs and HCHs, the levels of HCB are very similar for the different sampling sites. This suggests that intensive usage of DDTs and HCHs following the earthquake had a significant effect on the levels of OCPs. Correlations identified between the enantiomers of the OCPs indicated that p,p'-DDTs and HCHs shared the same source, and that o,p'-DDT and HCB may come from similar sources. The signatures of OCPs suggested that the technical DDTs and HCHs used following the earthquake still contribute to their current levels in the atmosphere of Tangshan city.

Characterization of Two Passive Air Samplers for Per- and Polyfluoroalkyl Substances

Two passive air sampler (PAS) media were characterized under field conditions for the measurement of per- and polyfluoroalkyl substances (PFASs) in the atmosphere. The PASs, consisting of polyurethane foam (PUF) and sorbent-impregnated PUF (SIP) disks, were deployed for over one year in parallel with high volume active air samplers (HV-AAS) and low volume active air samplers (LV-AAS). Samples were analyzed for perfluoroalkyl carboxylic acids (PFCAs), perfluoroalkane sulfonic acids (PFSAs), fluorotelomer alcohols (FTOHs), fluorotelomer methacrylates (FTMACs), fluorotelomer acrylates (FTACs), perfluorooctane sulfonamides (FOSAs), and perfluorooctane sulfonamidoethanols (FOSEs). Sampling rates and the passive sampler medium (PSM)-air partition coefficient (KPSM-A) were calculated for individual PFASs. Sampling rates were similar for PFASs present in the gas phase and particle phase, and the linear sampling rate of 4 m(-3) d(-1) is recommended for calculating effective air sample volumes in the SIP-PAS and PUF-PAS for PFASs except for the FOSAs and FOSEs in the PUF-PAS. SIP disks showed very good performance for all tested PFASs while PUF disks were suitable only for the PFSAs and their precursors. Experiments evaluating the suitability of different isotopically labeled fluorinated depuration compounds (DCs) revealed that (13)C8-perfluorooctanoic acid (PFOA) was suitable for the calculation of site-specific sampling rates. Ambient temperature was the dominant factor influencing the seasonal trend of PFASs.