RESUMO
This paper integrates perspectives from analytical chemistry, environmental engineering, and industrial hygiene to better understand how workers may be exposed to perfluorinated carboxylic acids when handling them in the workplace in order to identify appropriate exposure controls. Due to the dramatic difference in physical properties of the protonated acid form and the anionic form, this family of chemicals provides unique industrial hygiene challenges. Workplace monitoring, experimental data, and modeling results were used to ascertain the most probable workplace exposure sources and transport mechanisms for perfluorooctanoic acid (PFOA) and its ammonium salt (APFO). PFOA is biopersistent and its measurement in the blood has been used to assess human exposure since it integrates exposure from all routes of entry. Monitoring suggests that inhalation of airborne material may be an important exposure route. Transport studies indicated that, under low pH conditions, PFOA, the undissociated (acid) species, actively partitions from water into air. In addition, solid-phase PFOA and APFO may also sublime into the air. Modeling studies determined that contributions from surface sublimation and loss from low pH aqueous solutions can be significant potential sources of workplace exposure. These findings suggest that keeping surfaces clean, preventing accumulation of material in unventilated areas, removing solids from waste trenches and sumps, and maintaining neutral pH in sumps can lower workplace exposures.
Assuntos
Poluentes Ocupacionais do Ar/química , Ácidos Carboxílicos/química , Fluorocarbonos/química , Exposição Ocupacional/prevenção & controle , Local de Trabalho/estatística & dados numéricos , Poluentes Ocupacionais do Ar/análise , Caprilatos/análise , Caprilatos/química , Ácidos Carboxílicos/análise , Indústria Química/estatística & dados numéricos , Descontaminação/métodos , Monitoramento Ambiental , Fluorocarbonos/análise , Humanos , Concentração de Íons de Hidrogênio , Modelos Químicos , Exposição Ocupacional/estatística & dados numéricos , Transição de Fase , Absorção Cutânea , Tensoativos/química , Pressão de VaporRESUMO
Perfluorooctanoate (PFO) is the anion of perfluorooctanoic acid. As the ammonium salt, PFO has been used for 50 years as a processing aid in the commercial production of perfluorinated and highly fluorinated polymers. To assess the effectiveness of industrial hygiene controls in processes involving PFO products and intermediates, a wipe test was developed and validated to determine quantitatively the PFO concentration on six surfaces: stainless steel, polycarbonate, Formica, butyl acid suit material, laminated disposable suit material, and a painted surface. Acceptable recovery and precision results were obtained for nonporous surfaces, such as stainless steel, polycarbonate, Formica, acid suit material, and painted surfaces on a 10-cm x 10-cm surface. The analytical method was evaluated over a range of 1 to 23 ng/cm2, or 100 to 2300 ng/100 cm2. The reporting limit for the method was 100 ng/wipe.
Assuntos
Caprilatos/análise , Monitoramento Ambiental/métodos , Poluentes Ambientais/análise , Fluorocarbonos/análise , Exposição Ocupacional/análise , Calibragem , Cromatografia Líquida/métodos , Monitoramento Ambiental/normas , Exposição Ocupacional/normas , Saúde Ocupacional , Controle de Qualidade , Propriedades de Superfície , Espectrometria de Massas em Tandem/métodosRESUMO
To determine the optimum conditions for the complete extraction of perfluorooctanoate (PFO) from polytetrafluoroethylene fluoropolymers, sample preparation and pressurized solvent extraction (PSE) conditions were investigated. Solvent extraction temperature, solvent residence time, relaxation time between extractions, and the effects of heating before PSE showed that methanol at 150 degrees C extraction temperature and a 12 min solvent residence time were the most efficient conditions. Preheating the polymer before extraction at 150 degrees C for 24 h significantly enhanced the quantity of PFO removed. Heating above 150 degrees C resulted in loss of PFO. PFO was determined by liquid chromatography with tandem mass spectrometry.