Adsorbent Tubes Research Articles

Variability in the Levels of BTEX at a Pollution Hotspot in New Delhi, India

It is a matter of concern that despite taking measures to control aromatic content in gasoline in India, the levels of volatile organic compounds are rising again in many of the Indian cities. The transport sector has been one of the major sectors which are re-sponsible for worsening the air quality of Delhi city. While thousands of toxic com-pounds are emitted from automobiles, industries, gasoline stations as well as service stations, however, volatile organic compounds are important due to their significant contribution to ozone formation, cancer, and non-cancer health risks. In this study, roadside levels of benzene, toluene, ethylbenzene and xylenes (BTEX) were investi-gated at the one of the major arterial road of Delhi city. Air samples were collected by activated coconut shell charcoal adsorbent tubes. The BTEX concentrations were de-termined by gas chromatography-flame ionization detector (GC-FID) technique. The mean concentrations of benzene, toluene, ethylbenzene and xylenes were, respectively, 60.22, 162.68, 49.42 and 25.25 μg/m3. The relative concentration distribution pattern and mutual correlation analysis indicated that in BTEX had sources other than vehicle emission at the study site. The samples collected, showed that BTEX had significantly higher concentrations in winter than those in spring and summer.

Atmospheric VOCs measurement in Nature Reserve Kopački rit, Croatia

To determine the impact of volatile organic compounds (VOCs) on ozone formation, their identification as well as air concentration assessment is necessary. These were one of the first collections on adsorption tube samples of VOCs in air from the Nature Reserve Kopacki rit. The samples were analysed by gas chromatography coupled with flame ionisation detector (FID) and mass selective detector (MSD), and results for the hydrocarbons with two to six carbon atoms are reported. The results show that among the measured concentrations, ethane, propane and n-butane were the highest. Biogenic hydrocarbon isoprene, whose concentrations follow daily cycle of ozone formation during the summer, was also identified and quantified. We used the cluster analysis (CA) to indentify the possible common emission sources among the measured data. The measured data are discussed in relation to the EU guidelines (Directive 2008/112/EC; Directive 2004/42/EC).

Emissions of Nanoparticles and Gaseous Material from 3D Printer Operation

This study evaluated the emissions characteristics of hazardous material during fused deposition modeling type 3D printing. Particulate and gaseous materials were measured before, during, and after 3D printing in an exposure chamber. One ABS and two PLA (PLA1 and PLA2) cartridges were tested three times. For online monitoring, a scanning mobility particle sizer, light scattering instrument, and total volatile organic compound (TVOC) monitor were employed and a polycarbonate filter and various adsorbent tubes were used for offline sampling. The particle concentration of 3D printing using ABS material was 33-38 times higher than when PLA materials were used. Most particles were nanosize (<100 nm) during ABS (96%) and PLA1 (98%) use, but only 12% were nanosize for PLA2. The emissions rates were 1.61 × 10(10) ea/min and 1.67 × 10(11) ea/g cartridge with the ABS cartridge and 4.27-4.89 × 10(8) ea/min and 3.77-3.91 × 10(9) ea/g cartridge with the PLA cartridge. TVOCs were also emitted when the ABS was used (GM; 155 ppb, GSD; 3.4), but not when the PLA cartridges were used. Our results suggest that more research and sophisticated control methods, including the use of less harmful materials, blocking emitted containments, and using filters or adsorbents, should be implemented.

Measurement of breakthrough volumes of volatile chemical warfare agents on a poly(2,6-diphenylphenylene oxide)-based adsorbent and application to thermal desorption–gas chromatography/mass spectrometric analysis

To establish adequate on-site solvent trapping of volatile chemical warfare agents (CWAs) from air samples, we measured the breakthrough volumes of CWAs on three adsorbent resins by an elution technique using direct electron ionization mass spectrometry. The trapping characteristics of Tenax® TA were better than those of Tenax® GR and Carboxen® 1016. The latter two adsorbents showed non-reproducible breakthrough behavior and low VX recovery. The specific breakthrough values were more than 44 (sarin) L/g Tenax® TA resin at 20°C. Logarithmic values of specific breakthrough volume for four nerve agents (sarin, soman, tabun, and VX) showed a nearly linear correlation with the reciprocals of their boiling points, but the data point of sulfur mustard deviated from this linear curve. Next, we developed a method to determine volatile CWAs in ambient air by thermal desorption–gas chromatography (TD–GC/MS). CWA solutions that were spiked into the Tenax TA® adsorbent tubes were analyzed by a two-stage TD–GC/MS using a Tenax® TA-packed cold trap tube. Linear calibration curves for CWAs retained in the resin tubes were obtained in the range between 0.2pL and 100pL for sarin, soman, tabun, cyclohexylsarin, and sulfur mustard; and between 2pL and 100pL for VX and Russian VX. We also examined the stability of CWAs in Tenax® TA tubes purged with either dry or 50% relative humidity air under storage conditions at room temperature or 4°C. More than 80% sarin, soman, tabun, cyclohexylsarin, and sulfur mustard were recovered from the tubes within 2 weeks. In contrast, the recoveries of VX and Russian VX drastically reduced with storage time at room temperature, resulting in a drop to 10–30% after 2 weeks. Moreover, we examined the trapping efficiency of Tenax TA® adsorbent tubes for vaporized CWA samples (100mL) prepared in a 500mL gas sampling cylinder. In the concentration range of 0.2–2.5mg/m3, >50% of sarin, soman, tabun, cyclohexylsarin, and HD were recovered, whereas <1% of VX and Russian VX were recovered in the same concentration range. The results indicate that CWA vapors, with the exception of VX and Russian VX, can be measured by an on-site collection procedure using the Tenax® TA resin tubes, followed by a subsequent TD–GC/MS analysis.

Electrocautery Devices With Feedback Mode and Teflon-Coated Blades Create Less Surgical Smoke for a Quality Improvement in the Operating Theater.

Monopolar electrocautery is a fast and elegant cutting option. However, as it creates surgical smoke containing polycyclic aromatic hydrocarbons (PAHs), it may be hazardous to the health of the surgical team. Although new technologies, such as feedback mode (FM) and Teflon-coated blades (TBs), reduce tissue damage, their impact on surgical smoke creation has not yet been elucidated. Therefore, we analyzed the plume at its source.The aim of this study was to evaluate if electrocautery FM and TBs create less surgical smoke.Porcine tissue containing skin was cut in a standardized manner using sharp-edged Teflon-coated blades (SETBs), normal-shaped TBs, or stainless steel blades (SSBs). Experiments were performed using FM and pure-cut mode. Surgical smoke was sucked through filters or adsorption tubes. Subsequently, filters were scanned and analyzed using a spectrophotometer. A high-performance liquid chromatography (HPLC-UV) was performed to detect benzo[a]pyrene (BaP) and phenanthrene as 2 of the most critical PAHs. Temperature changes at the cutting site were measured by an infrared thermometer.In FM, more surgical smoke was created using SSB compared with TBs (P < 0.001). Furthermore, differences between FM and pure-cut mode were found for SSB and TB (P < 0.001), but not for SETB (P = 0.911). Photometric analysis revealed differences in the peak heights of the PAH spectrum. In HLPC-UV, the amount of BaP and phenanthrene detected was lower for TB compared with SSB. Tissue temperature variations increased when SSB was used in FM and pure-cut mode. Furthermore, different modes revealed higher temperature variations with the use of SETB (P = 0.004) and TB (P = 0.005) during cutting, but not SSB (P = 0.789).We found that the use of both TBs and FM was associated with reduced amounts of surgical smoke created during cutting. Thus, the surgical team may benefit from the adoption of such new technologies, which could contribute to the primary prevention of smoke-related diseases.

Investigation of Polycyclic Aromatic Hydrocarbons (PAHs) and Methoxyphenols (MPs) from laboratory scale thermal oxidation of waste wood samples

In the present study, Polycyclic Aromatic Hydrocarbons (PAHs) and Methoxyphenols (MPs) emitted from the low temperature oxidation of the waste wood samples were identified in the laboratory scale small burning system. Four types of waste wood including untreated hardwood (HW), untreated softwood (SW), treated roof material (RM) and treated window frame (WF) were examined during the experiments. XAD-2 adsorbent tubes were used for sampling of the gaseous combustion products. After extraction of the sample tubes, extracts were analyzed by using the Hewlett Packard 6890 GC coupled with Agilent 5971 Mass Selective (MS) Detector. The relative average contributions of the naphthalene, acenaphthylene and retene in hardwood samples were found higher than those measured in softwood. On the contrary, the relative average contribution of the phenanthrene, anthracene, fluoranthene, benzo(a)anthracene, chrysene and benzo(b)fluoranthene to the total PAH concentration in softwood samples were obtained higher as compared to hardwood sample. Syringol, 4-methyl syringol, 4 methyl guaiacol, eugenol, properlysyringol, 4-ethylsyringol, syringylacetone and iso-eugenol were found to be most abundant compounds in the hardwood samples. On the other hand, the most observed compounds in the softwood samples were 4-methylguacicol, iso-eugenol, guaiacol, eugenol and vanillin.

Measurement of carbonyls in exhaust gases of light-duty vehicles in China using pentafluorophenyl hydrazine derivatisation and GC/MS analysis

A method for determining carbonyl emissions from motor vehicles was developed in which exhaust gases from test vehicles running on a dynamometer are directly collected in 6-L Teflon bags and then introduced into pentafluorophenyl hydrazine -coated adsorbent tubes for derivatisation and subsequent analysis of generated derivatives by GC/MS. Twenty gasoline and LPG light-duty vehicles were sampled at a vehicle inspection station in Guangzhou, China, by running test vehicles over a transient testing cycle and analysed for carbonyls. Results show that the method can achieve a detection limit of 8–28 ng m−3 for individual carbonyls with a relative standard deviation of 14.5%. Twenty-four carbonyls were identified in the gasoline vehicle exhaust gases and their total concentration was 19.2 mg m−3. For the LPG vehicles, 20 carbonyls were found in the exhaust gases with a total concentration of 4.71 mg m−3. Based on the results, carbonyl emission factors for the gasoline and LPG vehicles were estimated to be 25.0 and 7.36 mg km−1, respectively.

On scope of improving solid sorption cooling—generating it continuously in a regenerative single adsorbent column

An experimental study relating generation of continuous solid sorption cooling in a single adsorbent tube is described in this article. Quick periodic pressurization and depressurization of an adsorbent column generates differential cooling between the two ends of the column. Based on a critical review of previous research findings, however, few modifications have been found necessary in the existing process design. Experiments conducted earlier have indicated that significant cooling is available within activated carbon inside the bed. To retrieve this cooling, the system has been modified to a regenerative-type cooling cycle. On the basis of theoretical recommendation, a carbon dioxide-activated carbon pair has been chosen for the present study, aiming at cooling for nearly room temperature applications. Results not only indicate noticeable improvement from its previous design, they seem to be quite promising.

An airborne perfluorocarbon tracer system and its first application for a Lagrangian experiment

Abstract. A perfluorocarbon tracer system (PERTRAS), specifically designed for Lagrangian aircraft experiments, has been developed by the Deutsches Zentrum für Luft- und Raumfahrt (German Aerospace Center, DLR). It consists of three main parts: a tracer release unit (RU), an adsorption tube sampler (ATS), and a tracer analytical system. The RU was designed for airborne tracer release experiments; meanwhile, it can be used on various platforms for different experimental purposes (here research vessel). PERTRAS was for the first time applied in the field campaign Stratospheric ozone: Halogen Impacts in a Varying Atmosphere (SHIVA) in November 2011. An amount of 8.8 kg perfluoromethylcyclopentane (PMCP) was released aboard the research vessel Sonne (RV Sonne) near the operational site of this campaign, Miri, Malaysia, on 21 November. The tracer samples collected using the ATS onboard the DLR research aircraft Falcon were analyzed in the laboratory using a thermal desorber–gas chromatography–mass spectrometry (TD–GC–MS) system. Guided by forecasts calculated with the Lagrangian model Hybrid Single Particle Lagrangian Integrated Trajectory (HYSPLIT), 64 tracer samples were collected onboard the Falcon approximately 5 and 25 h after the release, mostly with a time resolution of 1 min. Enhanced PMCP concentrations relative to ambient PMCP background values (mean: 6.62 fmol mol−1) were detected during three intersects of the fresh tracer plume (age 5 h), with a maximum value of 301.33 fmol mol−1. This indicates that the fresh tracer plume was successfully intercepted at the forecast position. During the second flight, 25 h after the release, the center of tracer plume was not detected by the sampling system due to a faster advection of the plume than forecast. The newly developed PERTRAS system has been successfully deployed for the first time. The instrumental setup and comparisons between the measurements and HYSPLIT simulations are presented in this study.

Activated Carbon-hydrogen based Continuous Sorption Cooling in Single Adsorbent Bed with LN2 Heat Sink

Quick and periodic inflow-outflow of adsorbate in an adsorbent column createsa differential temperature between the two ends of it, allowing for the generation of continuous sorption cooling in a single adsorbent tube. The concept has been proven experimentally and theoretically for near room temperature applications using activated carbon-nitrogen. The feasibility of generating continuous solid sorption cooling in a single adsorbent tube in the cryogenic domainhas been studied theoretically with a different adsorbent-adsorbate pair, namely, activated carbon-hydrogen. Precooling of gaseous hydrogen (before it enters the adsorbent column) and removal of the heat of adsorption has been achieved using liquid nitrogen. Theoretical estimation shows nearly 20 K temperature difference between the two ends under no load condition. Finally, parametric variations have been performed.

Analysis of Benzene Exposure Levels on Commuters Traveling within the Metropolitan Area of Costa Rica

This study reports the benzene exposure levels of commuters traveling within the metropolitan area of Costa Rica using personal cars, buses, and urban trains. 47 in-vehicle samples were col- lected in the 2014 wet season under three different driving conditions: rush hour traffic, normal traffic and weekends. Samples were collected in Tedlar bags and analyzed using 75 µm carboxen- polydimethylsiloxane (CAR/PDMS) and gas chromatography with flame ionization detection (GC- FID). Additionally, duplicate samples were collected on adsorption tubes filled with Tenax TA and analyzed by thermal desorption (TD) and GC-FID. Results indicate that travelling in cars and buses under rush hour conditions exposes commuters to statistically equal average benzene concentra- tion of 48.7 and 51.6 µg/m3, respectively. Average benzene levels in urban trains (33.0 µg/m3) were measured only during morning rush hours. Greater benzene levels in buses than personal cars concentrations may be attributable to the immersion of traffic-related emission within the bus ca- bins. Factors, such as the driving pattern, the number of vehicles on the route, the road infrastruc- ture, and the prevalence of gasoline-fueled vehicles in Costa Rica, may increase ambient benzene concentrations. Benzene levels inside car cabins reported in this study are in the range of those reported in other urban areas; however, the corresponding concentrations inside buses and urban trains (rush hour only) are higher than previously published exposure levels.

Identification of Volatile Organic Compounds in Several Indoor Public Places in Korea

A comprehensive profile of volatile organic compounds (VOCs) in public spaces is needed for interpreting indoor air measurements. Seasonal differences in profiles are critical for epidemiological study and risk assessment. The purposes of this study were to establish profiles for individual VOCs in 50 indoor public places in Korea and to determine seasonal variations in their concentrations. Air samples were taken during working hours. Seventy-two of the 91 targeted VOCs were identified using multiple standards. Six VOCs detected in all summer and winter samples were toluene, acetone, m,p-xylenes, ethylbenzene, benzene, and styrene. In summer, methyl ethyl ketone and 1-butanol were also found in all samples. In both seasons, the dominant indoor VOCs were toluene, m,p-xylenes, ethylbenzene, acetone, and isopropyl alcohol. Other chemicals associated with gasoline emissions were dominant in summer. Limonene was dominant only in winter due to the consumption of tangerines. The nine VOCs with the highest concentrations comprised 64.8% and 49.6% of the TVOC in summer and winter, respectively. Comparing two types of adsorbent tube, a single adsorbent tube with Tenax-TA had similar detection performance as a double adsorbent tube with Tenax and Carbotrap.

실내공기질 공정시험법 중 VOCs 측정방법의 문제점 고찰 및 개선방안에 관한 연구

During the last two decades, indoor air quality and volatile organic compounds (VOCs) have been of concern in Korean society due to their nature of potential health impacts. In order to investigate the pollution levels of VOCss in indoor environments, establishment of a solid test method for monitoring the airborne VOCss is essential. In Korea, a method based on adsorbent sampling and GC analysis coupled with thermal desorption was proclaimed as the Korea Standard Method for Indoor Air Quality Test. This study was carried out to examine some inherent problems of the VOCs measurement method. The VOCs method does not describe in detail preparing the standard samples. The standard samples may be prepared by impregnation of either liquid standard solutions or a mixture of standard gases. In this study, we investigated the optimal temperature condition for transferring the liquid standards onto a standard adsorbent tube. As a result, keeping the impregnation temperature at 250℃ will be recommended in regard of the boiling points of multiple target analytes and the thermal stability of the adsorbent. We also demonstrated some problems associated with handling of a syringe used for transferring the standard solutions onto the adsorbent tubes, and a best way to get rid of the syringe problems was suggested. Finally, a number of field works were conducted to evaluate the performance of adsorbent sampling methods. Comparison of different adsorbent tubes, i.e. tube packed with single sorbent (Tenax) and double sorbents (Tenax with Carbotrap), revealed that 30 to 40% differences between the two groups, implying that sampling efficiency is depending on the volatility and the strength of adsorbents. However, duplicate precisions for VOCs sampling with a same type of adsorbent and at same flow rates appeared to be satisfactory to be all within 20%, which is a quality control guideline. Distributed volume precisions were also found to be within a guideline value, 25%, although the precision was in general inferior to the duplicate precision. The Korea indoor VOCs test method should be more refined and improved in many aspects, particularly procedure and instrumentation for preparing the standard samples and specification of quality control assessment.

Determination of sevoflurane and isopropyl alcohol in exhaled breath by thermal desorption gas chromatography–mass spectrometry for exposure assessment of hospital staff

Volatile anaesthetics and disinfection chemicals pose ubiquitous inhalation and dermal exposure risks in hospital and clinic environments. This work demonstrates specific non-invasive breath biomonitoring methodology for assessing staff exposures to sevoflurane (SEV) anaesthetic, documenting its metabolite hexafluoroisopropanol (HFIP) and measuring exposures to isopropanol (IPA) dermal disinfection fluid. Methods are based on breath sample collection in Nalophan bags, followed by an aliquot transfer to adsorption tube, and subsequent analysis by thermal desorption gas chromatography–mass spectrometry (TD-GC–MS). Ambient levels of IPA were also monitored. These methods could be generalized to other common volatile chemicals found in medical environments. Calibration curves were linear (r2=0.999) in the investigated ranges: 0.01–1000ppbv for SEV, 0.02–1700ppbv for IPA, and 0.001–0.1ppbv for HFIP. The instrumental detection limit was 10pptv for IPA and 5pptv for SEV, both estimated by extracted ion-TIC chromatograms, whereas the HFIP minimum detectable concentration was 0.5pptv as estimated in SIM acquisition mode. The methods were applied to hospital staff working in operating rooms and clinics for blood draws. SEV and HFIP were present in all subjects at concentrations in the range of 0.7–18, and 0.002–0.024ppbv for SEV and HFIP respectively. Correlation between IPA ambient air and breath concentration confirmed the inhalation pathway of exposure (r=0.95, p<0.001) and breath-borne IPA was measured as high as 1500ppbv. The methodology is easy to implement and valuable for screening exposures to common hospital chemicals. Although the overall exposures documented were generally below levels of health concern in this limited study, outliers were observed that indicate potential for acute exposures.

Evaluation of sorbent materials for the sampling and analysis of phosphine, sulfuryl fluoride and methyl bromide in air

Phosphine (PH3), sulfuryl fluoride (SO2F2) and methyl bromide (CH3Br) are highly toxic chemical substances commonly used for fumigation, i.e., pest control with gaseous pesticides. Residues of fumigation agents constitute a health risk for workers affected, and therefore accurate methods for air sampling and analysis are needed. In this study, three commercial adsorbent tubes; Carbosieve SIII™, Air Toxics™ and Tenax TA™, were evaluated for sampling these highly volatile chemicals in air and their subsequent analysis by thermal desorption–gas chromatography–mass spectrometry (TD–GC–MS). The breakthrough volume (BTV) of each fumigant was experimentally determined on the different adsorbents at concentrations at or above their permissible exposure limits, using a method based on frontal chromatography of generated fumigant atmospheres. Carbosieve SIII™, a molecular sieve possessing a very high specific area, proved to be a better adsorbent than both Air Toxics™ and Tenax TA™, resulting in at least a 4-fold increase of the BTV50%. BTV50% for Carbosieve SIII™ at 20°C was measured as 4.7L/g, 5.5L/g and 126L/g for phosphine, sulfuryl fluoride and methyl bromide, respectively, implying safe sampling volumes of 1.9L, 2.2L and 50L, respectively, for a commercial tube packed with 800mg Carbosieve SIII™. The temperature dependence of BTV was strong for Carbosieve SIII™, showing a reduction of 3–5%/°C in breakthrough volume within the range −20 to 40°C. Furthermore, although Carbosieve SIII™ reportedly has a higher affinity for water than most other adsorbents, relative humidity had only a moderate influence on the retention capacity of phosphine. Overall, the applicability of Carbosieve SIII™ adsorbent sampling in combination with TD–GC–MS analysis was demonstrated for highly volatile fumigants.

Aggregate dermal exposure to cyclic siloxanes in personal care products: Implications for risk assessment

Consumers who use personal care products (PCPs) are internally exposed to some of the organic components present of which some may be detected in exhaled air when eliminated. The aim of this study was the quantitative determination of octamethylcyclotetrasiloxane (D4) and decamethylcyclopentasiloxane (D5) in end-exhaled air to study dermal absorption of substances in PCPs. We exposed the forearm of fifteen healthy volunteers for 60min to pure D4 or D5 and to commercial products containing D4 and D5. Inhalation uptake was kept to a minimum by keeping the forearm in a flow cabinet during dermal exposure and supplying filtered air to the breathing zone of the volunteer during the post-exposure period. End-exhaled air was collected using a breath sampler (Bio-VOC), transferred to carbograph multi-bed adsorbent tubes and analyzed by thermal desorption gas chromatography mass spectrometry (TD-GC-MS). In the end-exhaled air of non-exposed volunteers background concentrations of D4 (0.8–3.5ng/L) and D5 (0.8–4.0ng/L) were observed. After exposing the volunteers, the level of D4 and D5 in end-exhaled air did not or barely exceed background concentrations. At t=90min, a sharp increase of the D4/D5 concentration in end-exhaled air was observed, which we attributed to the inhalation of the substances during a toilet visit without using inhalation protection devices. When this visit was taken out of the protocol, the sharp increase disappeared. Overall, the results of our study indicate that dermal absorption of D4 and D5 contributes only marginally to internal exposure following dermal applications. As in our study inhalation is the primary route of entry for these compounds, we conclude that its risk assessment should focus on this particular exposure route.

Occupational Exposures through Inhalation and Dermal Contact among Hot Asphalt Roofers in Denver

Construction work has been repeatedly linked to occupational cancers and roofers are among the most vulnerable group in this industry. Work with hot asphalt has been the main concern, but co-exposure to coal tar is viewed as a significant confounder. This study fills an important research gap by quantifying exposures to polycyclic aromatic hydrocarbons (PAH) through inhalation and dermal routes. Twenty roofers have been recruited from a construction site at the Air Force Academy in Colorado. Information on work and task related factors and use of personal protective equipment were collected via questionnaires. Blood and urine samples and dermal wipes (sunflower oil) have been collected on two work days, before and after 6h of work. Particle-bound PAHs have been collected using personal pumps fitted with PM2.5 sampling inlets (37 mm Teflon filters) during the work hours. Gas-phase PAHs were collected using standard adsorbent tubes (XAD-2, 75/150 mg) with sample flow rate set at 2.7 L/min. The presence of coal tar in roof core was determined using a fluorescence scan. Levels of individual PAHs are being analyzed from air, plasma, urine samples (all with GC/MS) and dermal wipes (GC/TOFMS). Our early results suggest that smaller molecular PAHs, such as naphthalene (median 241.9 and 364.6 ng/m3 on day 1 and 2, respectively) and phenanthrene (median 48.7 and 90 ng/m3 on day 1 and 2, respectively) are the most abundant PAH in gaseous phase. We observed strong correlations between air levels of gaseous PAHs, such as naphthalene, phenanthrene, pyrene and anthracene (Spearman coefficients between 0.527 and 0.943 for, p&lt;0.05 for all). Plasma PAHs were mostly below the quantification limit on both study days. Even though analyses of roof core samples did not indicate the presence of coal tar, 4-6 ring PAHs appear to predominate dermal wipe extracts.

Exploratory breath analyses for assessing toxic dermal exposures of firefighters during suppression of structural burns

Firefighters wear fireproof clothing and self-contained breathing apparatus (SCBA) during rescue and fire suppression activities to protect against acute effects from heat and toxic chemicals. Fire services are also concerned about long-term health outcomes from chemical exposures over a working lifetime, in particular about low-level exposures that might serve as initiating events for adverse outcome pathways (AOP) leading to cancer. As part of a larger US National Institute for Occupational Safety and Health (NIOSH) study of dermal exposure protection from safety gear used by the City of Chicago firefighters, we collected pre- and post-fire fighting breath samples and analyzed for single-ring and polycyclic aromatic hydrocarbons as bioindicators of occupational exposure to gas-phase toxicants. Under the assumption that SCBA protects completely against inhalation exposures, any changes in the exhaled profile of combustion products were attributed to dermal exposures from gas and particle penetration through the protective clothing. Two separate rounds of firefighting activity were performed each with 15 firefighters per round. Exhaled breath samples were collected onto adsorbent tubes and analyzed with gas-chromatography-mass spectrometry (GC-MS) with a targeted approach using selective ion monitoring. We found that single ring aromatics and some PAHs were statistically elevated in post-firefighting samples of some individuals, suggesting that fire protective gear may allow for dermal exposures to airborne contaminants. However, in comparison to a previous occupational study of Air Force maintenance personnel where similar compounds were measured, these exposures are much lower suggesting that firefighters’ gear is very effective. This study suggests that exhaled breath sampling and analysis for specific targeted compounds is a suitable method for assessing systemic dermal exposure in a simple and non-invasive manner.

Ambient aromatic hydrocarbon measurements at Welgegund, South Africa

Abstract. Aromatic hydrocarbons are associated with direct adverse human health effects and can have negative impacts on ecosystems due to their toxicity, as well as indirect negative effects through the formation of tropospheric ozone and secondary organic aerosol, which affect human health, crop production and regional climate. Measurements of aromatic hydrocarbons were conducted at the Welgegund measurement station (South Africa), which is considered to be a regionally representative background site. However, the site is occasionally impacted by plumes from major anthropogenic source regions in the interior of South Africa, which include the western Bushveld Igneous Complex (e.g. platinum, base metal and ferrochrome smelters), the eastern Bushveld Igneous Complex (platinum and ferrochrome smelters), the Johannesburg–Pretoria metropolitan conurbation (&gt; 10 million people), the Vaal Triangle (e.g. petrochemical and pyrometallurgical industries), the Mpumalanga Highveld (e.g. coal-fired power plants and petrochemical industry) and also a region of anticyclonic recirculation of air mass over the interior of South Africa. The aromatic hydrocarbon measurements were conducted with an automated sampler on Tenax-TA and Carbopack-B adsorbent tubes with heated inlet for 1 year. Samples were collected twice a week for 2 h during daytime and 2 h during night-time. A thermal desorption unit, connected to a gas chromatograph and a mass selective detector was used for sample preparation and analysis. Results indicated that the monthly median (mean) total aromatic hydrocarbon concentrations ranged between 0.01 (0.011) and 3.1 (3.2) ppb. Benzene levels did not exceed the local air quality standard limit, i.e. annual mean of 1.6 ppb. Toluene was the most abundant compound, with an annual median (mean) concentration of 0.63 (0.89) ppb. No statistically significant differences in the concentrations measured during daytime and night-time were found, and no distinct seasonal patterns were observed. Air mass back trajectory analysis indicated that the lack of seasonal cycles could be attributed to patterns determining the origin of the air masses sampled. Aromatic hydrocarbon concentrations were in general significantly higher in air masses that passed over anthropogenically impacted regions. Inter-compound correlations and ratios gave some indications of the possible sources of the different aromatic hydrocarbons in the source regions defined in the paper. The highest contribution of aromatic hydrocarbon concentrations to ozone formation potential was also observed in plumes passing over anthropogenically impacted regions.

Analyses on influencing factors of airborne VOCS pollution in taxi cabins.

Due to the long time in vehicular cabins, people have high exposure to the airborne volatile organic compounds (VOCS), which will lead to negative effects on human health. In order to analyze the influencing factors of in-car VOCS pollution concentrations, 38 taxis were investigated on the static and closed conditions. The interior air of taxis was collected through activated Tenax adsorption tubes, and the air samples were analyzed with thermally desorbed gas chromatograph. The average concentrations of in-car benzene, toluene, ethylbenzene, xylenes, styrene, butyl acetate, undecane, and total VOCS (TVOC) were 82.7, 212.3, 74.7, 182.3, 24.7, 33.5, 61.3, and 1,441.7 μg/m(3), respectively. Furthermore, the VOCS and TVOC concentrations increase with the rise of in-car temperature and relative humidity, and decrease with the increase of car age and total mileage. In addition, the VOCS and TVOC concentrations are higher in vehicles with small cabins than in ones with big cabins, and change with different sampling sites and various vehicular grades. Finally, according to the multiple linear regression analysis and hierarchical cluster analysis, car age is the most important factor influencing airborne VOCS and TVOC pollution concentrations in vehicular cabins, followed by interior temperature and total mileage.