Troy M Benn’s research while affiliated with Arizona State University and other places

Combustion processes can form fullerenes (C60). Therefore we investigate the occurrence of C60 in various atmospheric environments. The detection and quantification is achieved with the highly specific and sensitive method of liquid chromatography coupled to mass spectrometry following solvent extraction of the samples. C60 was detected in the air particulates of a parking garage and the exhaust soot of a diesel truck. These results would indicate that fullerenes are incidentally produced from combustion processes and become associated with atmospheric particulate matter. However C60 is susceptible to atmospheric oxidation processes. In particular ozonation tests on solid C60 confirm the production of fullerene-based compounds such as C60O. Such oxidation and alteration of the molecular structure of the fullerenes would explain the low ambient concentrations observed respectively the inability to detect C60 in ambient air in many locations, further away from potential emission sources. These results have significant policy implications including considering incidental sources of C60 in addition to engineered C60 added to commercial products, and understanding environmental oxidation processes for C60 in conjunction with quantifying transformation products.

There is a growing concern about the human and environmental health effects of fullerenes (e.g., C(60)) due to their increasing application in research, medicine, and industry. Toxicological and pharmacokinetic research requires standard methods for extraction and detection of fullerenes from biological matrices such as urine. The present study validates the use of liquid-liquid extraction (LLE) and solid-phase extraction (SPE) methods in conjunction with liquid chromatography-mass spectrometry (LC-MS) for the quantitative determination of C(60) in human and synthetic urine as compared with ultrapure water. Glacial acetic acid, which is necessary to prevent emulsions during LLE, inhibited C(60) detection by LC-MS, but this could be mitigated with evaporation. Aqueous C(60) aggregates (nC(60)) were spiked at 180 μg/L into the components of a synthetic urine recipe to determine their individual impacts on extraction and detection. Urea, creatinine, and a complex protein (i.e., gelatin) were found to impair SPE, leading to a low recovery rate of 43 ± 4% for C(60) spiked into human urine. In contrast, C(60) was consistently recovered from synthetic matrices using LLE, and recovery in human urine was 80 ± 6%. These results suggest that LLE combined with LC-MS is suitable for studying the clearance of fullerenes from the body. LLE is a robust technique that holds promise for extracting C(60) from other complex biological matrices (e.g., blood, sweat, amniotic fluid) in toxicological studies, enabling a better understanding of the behavior of fullerenes in human and animal systems and facilitating a more comprehensive risk evaluation of fullerenes.

Fullerenes are sphere-like molecules with unique physico-chemical properties, which render them of particular interest in biomedical research, consumer products and industrial applications. Human and environmental exposure to fullerenes is not a new phenomenon, due to a long history of hydrocarbon-combustion sources, and will only increase in the future, as incorporation of fullerenes into consumer products becomes more widespread for use as anti-aging, anti-bacterial or anti-apoptotic agents.An essential step in the determination of biological effects of fullerenes (and their surface-functionalized derivatives) is establishment of exposure-assessment techniques. However, in ecotoxicological studies, quantification of fullerenes is performed infrequently because robust, uniformly applicable analytical approaches have yet to be identified, due to the wide variety of sample types. Moreover, the unique physico-chemistry of fullerenes in aqueous matrices requires reassessment of conventional analytical approaches, especially in more complex biological matrices (e.g., urine, blood, plasma, milk, and tissue).Here, we present a review of current analytical approaches for the quantification of fullerenes and propose a consensus approach for determination of these nanomaterials in a variety of environmental and biological matrices.

Environmental, health, and safety (EHS) concerns are receiving considerable attention in nanoscience and nanotechnology (nano) research and development (R&D). Policymakers and others have urged that research on nano's EHS implications be developed alongside scientific research in the nano domain rather than subsequent to applications. This concurrent perspective suggests the importance of early understanding and measurement of the diffusion of nano EHS research. The paper examines the diffusion of nano EHS publications, defined through a set of search terms, into the broader nano domain using a global nanotechnology R&D database developed at Georgia Tech. The results indicate that nano EHS research is growing rapidly although it is orders of magnitude smaller than the broader nano S&T domain. Nano EHS work is moderately multidisciplinary, but gaps in biomedical nano EHS's connections with environmental nano EHS are apparent. The paper discusses the implications of these results for the continued monitoring and development of the cross-disciplinary utilization of nano EHS research.

Nanosilver has become one of the most widely used nanomaterials in consumer products because of its antimicrobial properties. Public concern over the potential adverse effects of nanosilver's environmental release has prompted discussion of federal regulation. In this paper, we assess several classes of consumer products for their silver content and potential to release nanosilver into water, air, or soil. Silver was quantified in a shirt, a medical mask and cloth, toothpaste, shampoo, detergent, a towel, a toy teddy bear, and two humidifiers. Silver concentrations ranged from 1.4 to 270,000 microg Ag g product(-1). Products were washed in 500 mL of tap water to assess the potential release of silver into aqueous environmental matrices (wastewater, surface water, saliva, etc.). Silver was released in quantities up to 45 microg Ag g product(-1), and size fractions were both larger and smaller than 100 nm. Scanning electron microscopy confirmed the presence of nanoparticle silver in most products as well as in the wash water samples. Four products were subjected to a toxicity characterization leaching procedure to assess the release of silver in a landfill. The medical cloth released an amount of silver comparable to the toxicity characterization limit. This paper presents methodologies that can be used to quantify and characterize silver and other nanomaterials in consumer products. The quantities of silver in consumer products can in turn be used to estimate real-world human and environmental exposure levels.

We studied the occurrence, characterization, and removal of nano- and larger-sized titanium (Ti) in a full-scale wastewater treatment plant. Raw sewage contained 100 – 3,000 μg/L Ti, while tertiary effluent Ti concentrations ranged from about 10 to 100 μg/L. The Ti that was removed across the treatment train accumulated in plant solids. Finished plant biosolids, tertiary effluent, and commercial toothpaste were analyzed by scanning electron microscopy, and various forms of Ti solids were observed, including aggregates containing nanoscale primary particles of titanium oxides. To support field work, laboratory batch sorption experiments were conducted with various types of nanoparticles as sorbates and wastewater biomass as sorbent. Upon exposure to 400 mg/L total suspended solids of wastewater biomass, 97% of silver nanoparticles 88% of fullerenes, 39% of functionalized nanosilver, 23% of nanoscale titanium dioxide, and only 13% of fullerol nanoparticles were removed.

The issues of water supply and management will become more and more critical as the global population increases. In order to meet future demands, water supply systems must be developed to maximize the use of locally available water. It is also important to minimize the impact of water system developments on the environment. In this study, the overall environmental impacts were compared for water importation, reclamation and seawater desalination to address the water scarcity in areas where local supplies are not sufficient. The city of Scottsdale, Arizona was chosen for this study. Life Cycle Assessment (LCA) was performed and it suggests that seawater desalination has the highest impact whereas reclamation shows a relatively lower impact. However, importation and reclamation systems have comparable results for several damage categories. The impacts of facility operations are significantly higher than the construction phase even when the life-span of infrastructure reduces from 50 year to 10 year. Due to the high impacts associated with the energy use during plant operations, different energy mixes were analyzed for their capabilities to lower the environmental burden.

Titanium (Ti) occurs naturally in soils and as highly purified titanium dioxide (Ti5O2) in many commercial products that have been used for decades. We report for the first time the occurrence, characterization, and removal of nano- and larger-sized Ti at wastewater treatment plants (WWTPs). At one WWTP studied in detail, raw sewage contained 100 to nearly 3000 microg TVL Ti larger than 0.7 microm accounted for the majority of the Ti in raw sewage, and this fraction was well removed by WWTP processes. Ti concentrations in effluents from this and several other WWTPs ranged from <5 to 15 microg/L and were nearly all present in the < 0.7 microm size fraction. As Ti was removed, it accumulated in settled solids at concentrations ranging from 1 to 6 microg Ti/mg. Ti-containing solids were imaged in sewage, biosolids, and liquid effluent as well as in commercial products containing engineered TiO2. Single nanoparticles plus spherical aggregates (50 nm to a few hundred nanometer in size) composed of sub-50 nm spheres of Ti and oxygen only (presumably TiO2) were observed in all samples. Significantly larger silicate particles containing a mixture of Ti and other metal atoms were also observed in the samples. To support the field work, laboratory adsorption batch and sequencing batch reactor experiments using TiO2 and activated sludge bacteria verified that adsorption of TiO2 onto activated sludge biomass occurs. Monitoring for TiO2 in the environment where WWTP liquid effluent is discharged (rivers, lakes, oceans) or biomass disposed (landfills, agriculture and soil amendments, incinerator off-gas or residuals) will increase our knowledge on the fate and transport of other nanomaterials in the environment

Manufacturers of clothing articles employ nanosilver (n-Ag) as an antimicrobial agent, but the environmental impacts of n-Ag release from commercial products are unknown. The quantity and form of the nanomaterials released from consumer products should be determined to assess the environmental risks of nanotechnology. This paper investigates silver released from commercial clothing (socks) into water, and its fate in wastewater treatment plants (WWTPs). Six types of socks contained up to a maximum of 1360 microg-Ag/g-sock and leached as much as 650 microg of silver in 500 mL of distilled water. Microscopy conducted on sock material and wash water revealed the presence of silver particles from 10 to 500 nm in diameter. Physical separation and ion selective electrode (ISE) analyses suggest that both colloidal and ionic silver leach from the socks. Variable leaching rates among sock types suggests that the sock manufacturing process may control the release of silver. The adsorption of the leached silver to WWTP biomass was used to develop a model which predicts that a typical wastewater treatment facility could treat a high concentration of influent silver. However, the high silver concentration may limitthe disposal of the biosolids as agricultural fertilizer.