The presence of erionite in North American geologies and the estimated mesothelioma potency by region.

OBJECTIVE: Erionite is a naturally occurring fibrous mineral found in soils in some geographical regions. Known for its potency for causing mesothelioma in the Cappadocia region of Turkey, the erionite fiber has attracted interest in the United States due to its presence in a band of rock that extends from Mexico to Montana. There are few toxicology studies of erionite, but all show it to have unusually high chronic toxicity. Despite its high potency compared to asbestos fibers, erionite has no occupational or environmental exposure limits. This paper takes what has been learned about the chemical and physical characteristics of the various forms of asbestos (chrysotile, amosite, anthophyllite, and crocidolite) and predicts the potency of North American erionite fibers. MATERIALS AND METHODS: Based on the fiber potency model in Korchevskiy et al. (2019) and the available published information on erionite, the estimated mesothelioma potency factors (the proportion of mesothelioma mortality per unit cumulative exposure (f/cc-year)) for erionites in the western United States were determined. RESULTS AND DISCUSSION: The model predicted potency factors ranged from 0.19 to 11.25 (average ∼3.5), depending on the region. For reference, crocidolite (the most potent commercial form of asbestos) is assigned a potency factor ∼0.5. CONCLUSION: The model predicted mesothelioma potency of Turkish erionite (4.53) falls in this same range of potencies as erionite found in North America. Although it can vary by region, a reasonable ratio of average mesothelioma potency based on this model is 3,000:500:100:1 comparing North American erionite, crocidolite, amosite, and chrysotile (from most potent to least potent).

Occupational exposures to asbestos in the steel industry: An analysis of the AISI sampling campaign (1989-1997).

The American Iron and Steel Institute (AISI) gathered data between 1989 and 1997 to build an "objective database" to further understand the occupational exposures generated by the few asbestos-containing materials remaining at various steelmaking companies at this time. This paper analyzed the 520 samples from this campaign which occurred at five different steel manufacturers: Georgetown Steel Company, Inland Steel Company, Ling-Temco-Vought (LTV) Corporation, United States Steel Corporation, and Weirton Steel Corporation. This database is believed to have never previously been systematically organized. Samples were grouped based on sampling times to determine whether they should most appropriately be compared to the OSHA short-term excursion limit (EL) or the 8-hr time-weighted average (TWA) permissible exposure limit (PEL). Sampling times of 30 min or less were considered short-term samples, and samples of 180 min or greater were considered representative workday samples. Samples that did not fit into either category, with sampling times between 31 and 179 min, were considered task samples. Overall, the data indicated that the airborne concentrations were quite low in 1989 and they continued to be low through the study period which ended in 1997. Only seven out of 286 (approximately 2.5%) short-term or representative workday samples were in exceedance of the current OSHA OELs that were implemented in 1994 (short-term samples being compared to the 1 f/cc EL and representative workday samples being compared to the 0.1 f/cc 8-hr TWA PEL). Consistent with prior data, analysis of this dataset supports the view that materials containing asbestos were not used in many applications in the steel industry, and measured airborne concentrations of asbestos were almost always below the occupational exposure limits (OELs) in the post-OSHA era (1972-2000).

Occupational exposure to asbestos in the steel industry (1972-2006).

BACKGROUND: Historically, the use of asbestos in steelmaking has been limited to a few applications. Due to its physical and chemical properties, asbestos was not necessary or suitable for most purposes in a steel mill. The few applications where asbestos were used (i.e., certain gaskets, brakes, protective cloth, refractory materials, insulation materials, and hot top products) were replaced by alternative materials as they became available. OBJECTIVE: We discuss historical uses of asbestos in steel manufacturing and the associated airborne asbestos concentrations collected at sixteen U. S. Steel facilities between 1972 and 2006. METHODS: A total of 495 personal airborne asbestos samples from the U. S. Steel industrial hygiene records were analyzed across four time periods corresponding to changes in the OSHA permissible exposure limit (PEL) for asbestos. 68% of the samples (n = 337) were considered representative of an employee's workday. The remaining samples (n = 158) represented task samples. Samples were grouped by facility, department, and job category within the four time periods. RESULTS: The average fiber concentrations measured for each facility and department over time were below the contemporaneous OSHA PEL. The mean representative workday asbestos air concentration from 1972 and 1975 was 1.09 f/cc. The mean representative workday concentration decreased to 0.13 f/cc between 1976 and 1985, then decreased again to 0.02 f/cc between 1986 and 1993 and 0.03 f/cc between 1994 and 2006. For task samples, the mean air concentration from 1972 to 1975 was 3.29 f/cc. The mean task sample concentration decreased to 0.48 f/cc between 1976 and 1985, then decreased again to 0.01 f/cc between 1986 and 1993 and 0.03 f/cc between 1994 and 2006. Only eleven out of the 495 samples (2.2%), for both task and representative workday samples, were in exceedance of the contemporaneous PEL(as an 8-hour TWA), ten of which occurred prior to 1978. Eight of these eleven PEL exceeding samples were task samples. Of the remaining three representative workday samples, two had unknown sampling times. IMPACT: This paper presents an analysis of all the available personal sampling data for airborne asbestos across 16 facilities of the U. S. Steel Corporation between 1972 and 2006. This dataset has previously never been publicly shared or analyzed. It represents one of the more complete industrial hygiene datasets from a corporation to be presented in a scientific journal and, due to the similarities in the processes at each mill, it should reflect analogous exposures throughout the steelmaking industry in the United States. One of the benefits of presenting these data is that it also provides insight into where asbestos-containing materials (ACMs) were used in the steel making process. This is just one example of a large firm that released information that had previously remained in file cabinets for decades. We believe that another benefit of publishing this paper is that it may encourage the largest firms in industry to assemble and analyze their industrial hygiene data to benefit the occupational hygiene, medical, and epidemiology communities. This can support future epidemiology studies and improve the design of future industrial hygiene programs.

Living at Work: 24-hour Noise Exposure Aboard US Navy Aircraft Carriers.

BACKGROUND: Personnel assigned to aircraft carriers are exposed to a variety of noise sources from equipment and flight deck operations for durations >12 h. Personnel work and live in environments where hazardous noise areas and hearing recovery spaces such as sleeping and relaxation areas are in proximity to one another which provides little recovery time from hazardous noise. This investigation describes noise levels measured over a 24-h period on a US Navy aircraft carrier during flight operations for different populations of aircraft carrier personnel. METHODS: Personal noise monitoring occurred from 23 to 28 January 2014 aboard a US Navy Nimitz-class aircraft carrier during a routine at-sea period. Fifty-nine study volunteers were assigned to similar exposure groups (SEGs). The SEGs were compared to determine which groups were at greatest risk of hazardous noise exposure. Statistical analysis was conducted with SPSS version 24 using an alpha level of 0.05. RESULTS: Mean 24-h equivalent continuous sound levels Leq(24-h) and on-duty time weighted averages (TWA(on-duty)) ranged from 71 to 127 decibels A weighted (dBA). The 80 dBA American Conference of Governmental Industrial Hygienists (ACGIH) threshold limit value (TLV) for 24-h noise exposure was exceeded by 93% of the study volunteers. The 85 dBA ACGIH TLV and Department of Defense Occupational exposure limit for 8-h noise exposures was exceeded by 68% of the population. Leq(off-duty) ranged from 38 to 102 dBA with 61% of the population exceeding the 70 dBA ACGIH TLV classified as effective quiet to allow for temporary threshold shift recovery. SEG 2 Flight Deck Launch and Recovery had significantly higher 24-h noise exposures than SEG 3 Damage Control Maintenance and Repair (P = 0.01), SEG 5 Supply (P = 0.01), and SEG 7 Administrative/Professional (P = 0.009). Similar results were found for TWA(on-duty) noise exposures. Median TWA(on-duty) and Leq(24-h) for SEG 2 were 16-21 dB higher than SEG 3, 5, and 7. There were no significant differences between off-duty Leq noise exposures according to SEG. DISCUSSION/CONCLUSIONS: SEGs located on the flight deck (SEGs 1 and 2) and SEGs responsible for maintenance and repair activities (SEGs 3 and 4) supporting flight operations had the highest TWA(on-duty) and Leq(24-h). These findings raise serious concerns because high noise exposures both on- and off-duty may result in immediate acoustic trauma and development of temporary threshold shifts, which, if unresolved with auditory rest, may lead to permanent hearing loss.

Determination of airborne concentrations of dichlorvos over a range of temperatures when using commercially available pesticide strips in a simulated military guard post.

Dichlorvos is a chemical compound which has been used for decades as a pesticide. Potential inhalational exposure to dichlorvos vapor associated with using commercially-based, dichlorvos-impregnated resin strips in a simulated military guard post was evaluated. A varying number of these pesticide strips, ranging from the manufacturer's guidelines ((3)-16 g strips) up to a full package of strips ((12)-16 g strips), were placed in a small, enclosed space (2.31 m x 2.26 m x 2.44 m, 12.7 m3), which was similar in size to a typical military guard post. Static air sampling was then conducted to simulate personal air sampling, followed by analysis using OSHA Method 62 (GC-ECD). Air sampling was conducted over a range of discrete temperatures (26-38˚C) which approximated average ambient temperatures expected in a variety of deployed environments. Air sampling in this range was conducted to determine the airborne concentration generated at each temperature setting. Airborne concentrations were then compared to established short term military exposure guidelines (MEGs) and the 8-hr OSHA permissible exposure limit (PEL) for dichlorvos (both criteria limits are 0.99 mg/m3). Results from air sampling indicated that exceeding the manufacturer-recommended number of strips for the workspace volume and environmental conditions produced airborne dichlorvos concentrations above established occupational standards (1.77-3.70 mg/m3). Such exposures may potentially lead to adverse effects, such as loss of mental and visual acuity for guard post watch standers who employ more strips within a space than recommended per the manufacturer for the size of the space. However, concentrations of airborne dichlorvos generated when adhering to manufacturer's guidelines based on workspace volume resulted in levels of 0.16-0.39 mg/m3 for 1-hr and 8-hr timeframes, which were below the established occupational health limits. While dichlorvos-impregnated strips are not currently recommended for use in manned workspaces for periods > 4 hr, findings suggest that prolonged use (8 hr) of similar pesticide strips within manned spaces to repel and/or kill disease-carrying insects may be possible without experiencing adverse health effects.

Short duration needle trap sampling with gas chromatography analysis to determine nearly instantaneous concentrations of selected organic vapor contaminants.

Needle trap device samplers were used for rapid (60 s) quantitative sampling of short-term exposure limit (STEL) and peak exposure standard concentrations using a manually operated pump to collect small volume (10 mL) gas phase samples containing methylene chloride, benzene, toluene, and tetrachloroethylene vapors. Solventless introduction of chemical samples for gas chromatography analysis with flame ionization detection yielded linear results (R(2) > 0.99) for vapor standard mixtures of the four target analytes ranging from 10% to 200% of their respective nominal STEL or peak exposure standard concentrations. Needle trap samplers showed ≥86% recovery (as GC-FID peak area responses) following 14-day storage at room temperature compared to the same samplers analyzed immediately, with better recovery values observed with shorter storage (≥95% at room temperature for seven days, except for methylene chloride) or with storage at 4°C. Calibration for quantitation of concentrations of benzene, toluene, and tetrachloroethylene was shown to be possible with the use of an internal standard to account for injector discrimination between the solventless NTD approach and injections of target analytes in carbon disulfide. Due to the simple sampling method (no field calibration and battery-free pumping) and the avoidance of solvent dilution, a needle trap sampling approach could simplify sample collection and analysis to chromatographically determine nearly instantaneous (1 min) exposure concentrations.

Application of a high surface area solid-phase microextraction air sampling device: collection and analysis of chemical warfare agent surrogate and degradation compounds.

This work examines a recently improved, dynamic air sampling technique, high surface area solid-phase microextraction (HSA-SPME), developed for time-critical, high-volume sampling and analysis scenarios. The previously reported HSA-SPME sampling device, which provides 10-fold greater surface area compared to commercially available SPME fibers, allowed for an increased analyte uptake per unit time relative to exhaustive sampling through a standard sorbent tube. This sampling device has been improved with the addition of a type-K thermocouple and a custom heater control circuit for direct heating, providing precise (relative standard deviation ∼1%) temperature control of the desorption process for trapped analytes. Power requirements for the HSA-SPME desorption process were 30-fold lower than those for conventional sorbent-bed-based desorption devices, an important quality for a device that could be used for field analysis. Comparisons of the HSA-SPME device when using fixed sampling times for the chemical warfare agent (CWA) surrogate compound, diisopropyl methylphosphonate (DIMP), demonstrated that the HSA-SPME device yielded a greater chromatographic response (up to 50%) relative to a sorbent-bed method. Another HSA-SPME air sampling approach, in which two devices are joined in tandem, was also evaluated for very rapid, low-level, and representative analysis when using discrete sampling times for the compounds of interest. The results indicated that subparts per billion by volume concentration levels of DIMP were detectable with short sampling times (∼15 s). Finally, the tandem HSA-SPME device was employed for the headspace sampling of a CWA degradation compound, 2-(diisopropylaminoethyl) ethyl sulfide, present on cloth material, which demonstrated the capability to detect trace amounts of a CWA degradation product that is estimated to be less volatile than sarin. The rapid and highly sensitive detection features of this device may be beneficial in decision making for law enforcement, military, and civilian emergency organizations and responders, providing critical information in a contaminated environment scenario when time is of the essence.