Per- and polyfluoroalkyl substances (PFAS), a highly persistent and potentially toxic class of chemicals, are added to cosmetics to increase their durability and water resistance. To assess this potential health and environmental risk, 231 cosmetic products purchased in the U.S. and Canada were screened for total fluorine using particle-induced gamma-ray emission spectroscopy. Of the eight categories tested, foundations, mascaras, and lip products had the highest proportion of products with high total fluorine ≥0.384 μg F/cm2. Twenty-nine products including 20 with high total fluorine concentrations were analyzed using targeted LC-MS/MS and GC-MS. PFAS concentrations ranged from 22–10,500 ng/g product weight, with an average and a median of 264 and 1050 ng/g product weights, respectively. Here, 6:2 and 8:2 fluorotelomer compounds, including alcohols, methacrylates, and phosphate esters, were most commonly detected. These compounds are precursors to PFCAs that are known to be harmful. The ingredient lists of most products tested did not disclose the presence of fluorinated compounds exposing a gap in U.S. and Canadian labeling laws. The manufacture, use, and disposal of cosmetics containing PFAS are all potential opportunities for health and ecosystem harm. Given their direct exposure routes into people, better regulation is needed to limit the widespread use of PFAS in cosmetics.

Occupational exposure to aqueous film-forming foams (AFFF) can lead to elevated concentrations of per-and polyfluorinated alkyl substances (PFAS) in firefighter blood sera. AFFF are also one exposure source of PFAS in the general population because of their environmental persistence and solubility in groundwater. Because of the documented adverse health effects of PFAS, the primary concern to date in the fire services has centered on repeated use and exposure to AFFF. In this work, an additional PFAS exposure source for firefighters is presented: PFAS that are shed from their protective clothing. Textiles used as firefighter turnout gear were found to have high levels of total fluorine (up to 2%), and individual PFAS were identified and measured on new and used firefighting turnout gear. Used gear showed lower levels of PFAS as well as an increased migration into untreated material. A dust measurement from a textile storage area also suggests direct loss of PFAS from the fluoropolymers in the textiles. Because PFAS that are shed from the textiles used in turnout gear are more mobile, they represent another viable exposure source for firefighters that warrants further study.

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A novel method for quickly and quantitatively measuring aqueous lead in drinking water has been developed. A commercially available activated carbon felt has been found to effectively capture lead from tap water, and partnered with X-ray fluorescence (XRF) spectrometry, it provides quantitative measurement of aqueous lead in drinking water. Specifically, for a 2 L volume of tap water, the linear range of detection was found to be from 1–150 ppb, encompassing the current EPA limit for lead in drinking water (15 ppb). To make a reproducible and easy to use method for filtering, a 2 L bottle cap with a 1.25 cm diameter hole was used for filtering. Utilizing this filtration method, 75 solutions from 0 to 150 ppb lead gave a 91% sensitivity, 97% specificity, and 93% accuracy, and all the misclassified samples fell between 10 and 15 ppb. This method has also proved reliable for detecting calcium as well as several other divalent metals in drinking water including copper, zinc, iron, and manganese.

Hazardous chemicals used in electronic and electrical consumer products can re-enter commerce when these products are recycled. The objectives of this study were to 1) identify the possible sources of unexpected chemicals and elements in consumer products, including the use of recycled E-waste plastics and 2) demonstrate bromine detection with nondestructive spectroscopy as an indicator of brominated flame retardants contaminating new products via recycled waste streams. More than 1500 consumer products of diverse types purchased in 2012-2014 were examined using X-ray fluorescence spectroscopy for correlations between bromine and other elements. New electronic products were much more likely than new non-electronics to contain greater than 1000 ppm bromine, consistent with intentionally added flame retardants, while nonelectronic products were more likely to contain between 5 and 100 ppm bromine, suggesting unintentional contamination. A typical suite of elements present in E-waste was found in a majority of plastic products. Two product categories, vinyl floor tiles and beaded necklaces/garlands, were explored in more detail. Specific flame retardant chemicals in bead samples were identified by mass spectrometry and their distribution in beads was studied using scanning electron microscopy and energy dispersive spectroscopy. Five brominated chemicals typically used as flame retardants, including BDE-209, were identified in 50 of 50 Mardi Gras beads analyzed.