Desiree L. Plata
Yale University
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Featured researches published by Desiree L. Plata.
Environmental Science & Technology | 2009
Desiree L. Plata; A. John Hart; Christopher M. Reddy; Philip M. Gschwend
The carbon nanotube (CNT) industry is expanding rapidly, yet little is known about the potential environmental impacts of CNT manufacture. Here, we evaluate the effluent composition of a representative multiwalled CNT synthesis by catalytic chemical vapor deposition (CVD) in order to provide data needed to design strategies for mitigating any unacceptable emissions. During thermal pretreatment of the reactant gases (ethene and H(2)), we found over 45 side-products were formed, including methane, volatile organic compounds (VOCs), and polycyclic aromatic hydrocarbons (PAHs). This finding suggests several environmental concerns with the existing process, including potential discharges of the potent greenhouse gas, methane (up to 1.7%), and toxic compounds such as benzene and 1,3-butadiene (up to 36000 ppmv). Extrapolating these laboratory-scale data to future industrial CNT production, we estimate that (1) contributions of atmospheric methane will be negligible compared to other existing sources and (2) VOC and PAH emissions may become important on local scales but will be small when compared to national industrial sources. As a first step toward reducing such unwanted emissions, we used continuous in situ measures of CNT length during growth and sought to identify which thermally generated compounds correlated with CNT growth rate. The results suggested that, in future CNT production approaches, key reaction intermediates could be delivered to the catalyst without thermal treatment. This would eliminate the most energetically expensive component of CVD synthesis (heating reactant gases), while reducing the formation of unintended byproducts.
Environmental Forensics | 2006
Robert K. Nelson; Brian M. Kile; Desiree L. Plata; Sean P. Sylva; Li Xu; Christopher M. Reddy; Richard B. Gaines; Glenn S. Frysinger; Stephen E. Reichenbach
Comprehensive two-dimensional gas chromatography (GC × GC) was used to investigate the Bouchard 120 oil spill. The latter occurred on April 25, 2003, when the barge Bouchard 120 spilled ∼ 375,000 liters of No. 6 fuel oil into Buzzards Bay, Massachusetts. In order to gain a better understanding of the natural processes affecting the fate of the spilled product, we collected and analyzed oil-covered rocks from Nyes Neck beach in North Falmouth, Massachusetts. Here we discuss the data from samples collected on May 9, 2003, and six months later, on November 23, 2003. Along with standard two-dimensional gas chromatographic analysis, we employed unique data-visualization techniques such as difference, ratio, and addition chromatograms to highlight how evaporation, water washing, and biodegradation weathered the spilled oil. These approaches provide a new perspective to studying oil spills and aid attempts to remediate them.
Environmental Science & Technology | 2014
Robert B. Jackson; Adrian Down; Nathan Phillips; Robert C. Ackley; Charles W. Cook; Desiree L. Plata; Kaiguang Zhao
Pipeline safety in the United States has increased in recent decades, but incidents involving natural gas pipelines still cause an average of 17 fatalities and
Proceedings of the National Academy of Sciences of the United States of America | 2015
Brian D. Drollette; Kathrin Hoelzer; Nathaniel R. Warner; Thomas H. Darrah; Osman Karatum; Megan P. O’Connor; Robert K. Nelson; Loretta A. Fernandez; Christopher M. Reddy; Avner Vengosh; Robert B. Jackson; Martin Elsner; Desiree L. Plata
133 M in property damage annually. Natural gas leaks are also the largest anthropogenic source of the greenhouse gas methane (CH4) in the U.S. To reduce pipeline leakage and increase consumer safety, we deployed a Picarro G2301 Cavity Ring-Down Spectrometer in a car, mapping 5893 natural gas leaks (2.5 to 88.6 ppm CH4) across 1500 road miles of Washington, DC. The δ(13)C-isotopic signatures of the methane (-38.2‰ ± 3.9‰ s.d.) and ethane (-36.5 ± 1.1 s.d.) and the CH4:C2H6 ratios (25.5 ± 8.9 s.d.) closely matched the pipeline gas (-39.0‰ and -36.2‰ for methane and ethane; 19.0 for CH4/C2H6). Emissions from four street leaks ranged from 9200 to 38,200 L CH4 day(-1) each, comparable to natural gas used by 1.7 to 7.0 homes, respectively. At 19 tested locations, 12 potentially explosive (Grade 1) methane concentrations of 50,000 to 500,000 ppm were detected in manholes. Financial incentives and targeted programs among companies, public utility commissions, and scientists to reduce leaks and replace old cast-iron pipes will improve consumer safety and air quality, save money, and lower greenhouse gas emissions.
Nature | 2016
John Liggio; Shao-Meng Li; Katherine Hayden; Youssef M. Taha; Craig Stroud; Andrea Darlington; Brian D. Drollette; Mark Gordon; Patrick A. Lee; Peter Liu; Amy Leithead; Samar G. Moussa; Danny Wang; Jason O’Brien; Richard L. Mittermeier; Jeffrey R. Brook; Gang Lu; Ralf M. Staebler; Yuemei Han; Travis W. Tokarek; Hans D. Osthoff; Paul A. Makar; Junhua Zhang; Desiree L. Plata; D. R. Gentner
Significance Organic compounds found in drinking water aquifers above the Marcellus Shale and other shale plays could reflect natural geologic transport processes or contamination from anthropogenic activities, including enhanced natural gas production. Using analyses of organic compounds coupled with inorganic geochemical fingerprinting, estimates of groundwater residence time, and geospatial analyses of shale gas wells and disclosed safety violations, we determined that the dominant source of organic compounds to shallow aquifers was consistent with surface spills of disclosed chemical additives. There was no evidence of association with deeper brines or long-range migration of these compounds to the shallow aquifers. Encouragingly, drinking water sources affected by disclosed surface spills could be targeted for treatment and monitoring to protect public health. Hundreds of organic chemicals are used during natural gas extraction via high-volume hydraulic fracturing (HVHF). However, it is unclear whether these chemicals, injected into deep shale horizons, reach shallow groundwater aquifers and affect local water quality, either from those deep HVHF injection sites or from the surface or shallow subsurface. Here, we report detectable levels of organic compounds in shallow groundwater samples from private residential wells overlying the Marcellus Shale in northeastern Pennsylvania. Analyses of purgeable and extractable organic compounds from 64 groundwater samples revealed trace levels of volatile organic compounds, well below the Environmental Protection Agency’s maximum contaminant levels, and low levels of both gasoline range (0–8 ppb) and diesel range organic compounds (DRO; 0–157 ppb). A compound-specific analysis revealed the presence of bis(2-ethylhexyl) phthalate, which is a disclosed HVHF additive, that was notably absent in a representative geogenic water sample and field blanks. Pairing these analyses with (i) inorganic chemical fingerprinting of deep saline groundwater, (ii) characteristic noble gas isotopes, and (iii) spatial relationships between active shale gas extraction wells and wells with disclosed environmental health and safety violations, we differentiate between a chemical signature associated with naturally occurring saline groundwater and one associated with alternative anthropogenic routes from the surface (e.g., accidental spills or leaks). The data support a transport mechanism of DRO to groundwater via accidental release of fracturing fluid chemicals derived from the surface rather than subsurface flow of these fluids from the underlying shale formation.
Environmental Science & Technology | 2016
Elijah J. Petersen; D. Xanat Flores-Cervantes; Thomas D. Bucheli; Lindsay C. C. Elliott; Jeffrey A. Fagan; Alexander Gogos; Shannon K. Hanna; Ralf Kägi; Elisabeth Mansfield; Antonio R. Montoro Bustos; Desiree L. Plata; Vytas Reipa; Paul Westerhoff; Michael R. Winchester
Worldwide heavy oil and bitumen deposits amount to 9 trillion barrels of oil distributed in over 280 basins around the world, with Canada home to oil sands deposits of 1.7 trillion barrels. The global development of this resource and the increase in oil production from oil sands has caused environmental concerns over the presence of toxic compounds in nearby ecosystems and acid deposition. The contribution of oil sands exploration to secondary organic aerosol formation, an important component of atmospheric particulate matter that affects air quality and climate, remains poorly understood. Here we use data from airborne measurements over the Canadian oil sands, laboratory experiments and a box-model study to provide a quantitative assessment of the magnitude of secondary organic aerosol production from oil sands emissions. We find that the evaporation and atmospheric oxidation of low-volatility organic vapours from the mined oil sands material is directly responsible for the majority of the observed secondary organic aerosol mass. The resultant production rates of 45-84 tonnes per day make the oil sands one of the largest sources of anthropogenic secondary organic aerosols in North America. Heavy oil and bitumen account for over ten per cent of global oil production today, and this figure continues to grow. Our findings suggest that the production of the more viscous crude oils could be a large source of secondary organic aerosols in many production and refining regions worldwide, and that such production should be considered when assessing the environmental impacts of current and planned bitumen and heavy oil extraction projects globally.
Environmental Science & Technology | 2015
Gordon J. Getzinger; Megan P. O’Connor; Kathrin Hoelzer; Brian D. Drollette; Osman Karatum; Marc A. Deshusses; P. Lee Ferguson; Martin Elsner; Desiree L. Plata
Carbon nanotubes (CNTs) have numerous exciting potential applications and some that have reached commercialization. As such, quantitative measurements of CNTs in key environmental matrices (water, soil, sediment, and biological tissues) are needed to address concerns about their potential environmental and human health risks and to inform application development. However, standard methods for CNT quantification are not yet available. We systematically and critically review each component of the current methods for CNT quantification including CNT extraction approaches, potential biases, limits of detection, and potential for standardization. This review reveals that many of the techniques with the lowest detection limits require uncommon equipment or expertise, and thus, they are not frequently accessible. Additionally, changes to the CNTs (e.g., agglomeration) after environmental release and matrix effects can cause biases for many of the techniques, and biasing factors vary among the techniques. Five case studies are provided to illustrate how to use this information to inform responses to real-world scenarios such as monitoring potential CNT discharge into a river or ecotoxicity testing by a testing laboratory. Overall, substantial progress has been made in improving CNT quantification during the past ten years, but additional work is needed for standardization, development of extraction techniques from complex matrices, and multimethod comparisons of standard samples to reveal the comparability of techniques.
Environmental Science & Technology | 2012
Desiree L. Plata; Christopher M. Reddy; Philip M. Gschwend
Volumes of natural gas extraction-derived wastewaters have increased sharply over the past decade, but the ultimate fate of those waste streams is poorly characterized. Here, we sought to (a) quantify natural gas residual fluid sources and endpoints to bound the scope of potential waste stream impacts and (b) describe the organic pollutants discharged to surface waters following treatment, a route of likely ecological exposure. Our findings indicate that centralized waste treatment facilities (CWTF) received 9.5% (8.5 × 10(8) L) of natural gas residual fluids in 2013, with some facilities discharging all effluent to surface waters. In dry months, discharged water volumes were on the order of the receiving body flows for some plants, indicating that surface waters can become waste-dominated in summer. As disclosed organic compounds used in high volume hydraulic fracturing (HVHF) vary greatly in physicochemical properties, we deployed a suite of analytical techniques to characterize CWTF effluents, covering 90.5% of disclosed compounds. Results revealed that, of nearly 1000 disclosed organic compounds used in HVHF, only petroleum distillates and alcohol polyethoxylates were present. Few analytes targeted by regulatory agencies (e.g., benzene or toluene) were observed, highlighting the need for expanded and improved monitoring efforts at CWTFs.
ACS Applied Materials & Interfaces | 2016
Osman Karatum; Stephen A. Steiner; Justin S. Griffin; Wenbo Shi; Desiree L. Plata
In spite of the growth of the carbon nanotube (CNT) industry, there are no established analytical methods with which to detect or quantify CNTs in environmental matrices. Given that CNTs have relatively high thermal stabilities, we investigated the use of thermal techniques to isolate and quantify single wall carbon nanotubes (SWCNTs). Test materials included ten types of commercial SWCNTs, representative biological macromolecules (bovine serum albumin and methylcellulose), soot, natural coastal sediments, and SWCNT-amended sediments. Different SWCNTs exhibited widely diverse degradation temperatures, and thermal analytical methods may require SWCNT-type specific parameters. To improve quantification capabilities, evolved gases were monitored by mass spectrometry. SWCNTs produced diagnostic ion ratios reflective of their high carbon and low hydrogen and oxygen contents. Current detection limits are roughly 4 μg(SWCNT) per sample (e.g., 100 μg(SWCNT) g(-1)(sediment) and 40 mg sample), controlled by interfering ions associated with the instruments non-airtight design. Although future modifications could improve this limitation, the current method is sufficient for quantifying SWCNTs in laboratories and industrial sites where SWCNTs are handled. Furthermore, the method shows promise to distinguish between incidental (e.g., soot) and engineered (e.g., SWCNTs) nanoparticles, which is not possible with current state-of-the-art techniques.
Journal of Chemical Ecology | 2001
Grant E. Brown; Justin L. Golub; Desiree L. Plata
More than 30 years separate the two largest oil spills in North American history (the Ixtoc I and Macondo well blowouts), yet the responses to both disasters were nearly identical in spite of advanced material innovation during the same time period. Novel, mechanically durable sorbents could enable (a) sorbent use in the open ocean, (b) automated deployment to minimize workforce exposure to toxic chemicals, and (c) mechanical recovery of spilled oils. Here, we explore the use of two mechanically durable, low-density (0.1-0.2 g cm(-3)), highly porous (85-99% porosity), hydrophobic (water contact angles >120°), flexible aerogel composite blankets as sorbent materials for automated oil capture and recovery: Cabot Thermal Wrap (TW) and Aspen Aerogels Spaceloft (SL). Uptake of crude oils (Iraq and Sweet Bryan Mound oils) was 8.0 ± 0.1 and 6.5 ± 0.3 g g(-1) for SL and 14.0 ± 0.1 and 12.2 ± 0.1 g g(-1) for TW, respectively, nearly twice as high as similar polyurethane- and polypropylene-based devices. Compound-specific uptake experiments and discrimination against water uptake suggested an adsorption-influenced sorption mechanism. Consistent with that mechanism, chemical extraction oil recoveries were 95 ± 2 (SL) and 90 ± 2% (TW), but this is an undesirable extraction route in decentralized oil cleanup efforts. In contrast, mechanical extraction routes are favorable, and a modest compression force (38 N) yielded 44.7 ± 0.5% initially to 42.0 ± 0.4% over 10 reuse cycles for SL and initially 55.0 ± 0.1% for TW, degrading to 30.0 ± 0.2% by the end of 10 cycles. The mechanical integrity of SL deteriorated substantially (800 ± 200 to 80 ± 30 kPa), whereas TW was more robust (380 ± 80 to 700 ± 100 kPa) over 10 uptake-and-compression extraction cycles.