James J. Jetter
United States Environmental Protection Agency
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Featured researches published by James J. Jetter.
Environmental Science & Technology | 2012
James J. Jetter; Yongxin Zhao; Kirk R. Smith; Bernine Khan; Tiffany L.B. Yelverton; P. F. DeCarlo; Michael D. Hays
Realistic metrics and methods for testing household biomass cookstoves are required to develop standards needed by international policy makers, donors, and investors. Application of consistent test practices allows emissions and energy efficiency performance to be benchmarked and enables meaningful comparisons among traditional and advanced stove types. In this study, 22 cookstoves burning six fuel types (wood, charcoal, pellets, corn cobs, rice hulls, and plant oil) at two fuel moisture levels were examined under laboratory-controlled operating conditions as outlined in the Water Boiling Test (WBT) protocol, Version 4. Pollutant emissions (carbon dioxide, carbon monoxide, methane, total hydrocarbons, and ultrafine particles) were continuously monitored. Fine particle mass was measured gravimetrically for each WBT phase. Additional measurements included cookstove power, energy efficiency, and fuel use. Emission factors are given on the basis of fuel energy, cooking energy, fuel mass, time, and cooking task or activity. The lowest PM(2.5) emissions were 74 mg MJ(delivered)(-1) from a technologically advanced cookstove compared with 700-1400 mg MJ(delivered)(-1) from the base-case open 3-stone cookfire. The highest thermal efficiency was 53% compared with 14-15% for the 3-stone cookfire. Based on these laboratory-controlled test results and observations, recommendations for developing potentially useful metrics for setting international standards are suggested.
Science of The Total Environment | 2002
James J. Jetter; Zhishi Guo; Jenia A. McBrian; Michael R. Flynn
The primary objective of this study was to improve the characterization of particulate matter emissions from burning incense. Emissions of particulate matter were measured for 23 different types of incense using a cyclone/filter method. Emission rates for PM2.5 (particulate matter less than 2.5 microm in aerodynamic diameter) ranged from 7 to 202 mg/h, and PM2.5 emission factors ranged from 5 to 56 mg/g of incense burned. Emission rates were also determined using an electrical low pressure impactor (ELPI) and a small electrostatic precipitator (ESP), and emission rates were compared to those determined using the cyclone/filter method. Emission rates determined by the ELPI method were consistently lower than those determined by the cyclone/filter method, and a linear regression correlation was found between emission rates determined by the two methods. Emission rates determined by the ESP method were consistently higher than those determined by the cyclone/filter method, indicating that the ESP may be a more effective method for measuring semivolatile particle emissions. A linear regression correlation was also found between emission rates determined by the ESP and cyclone/filter methods. Particle size distributions were measured with the ELPI, and distributions were found to be similar for most types of incense that were tested. Size distributions by mass typically ranged from approximately 0.06 to 2.5 microm in aerodynamic diameter, with peak values between 0.26 and 0.65 microm. Results indicated that burning incense emits fine particulate matter in large quantities compared to other indoor sources. An indoor air quality model showed that indoor concentrations of PM25 can far exceed the outdoor concentrations specified by the US EPAs National Ambient Air Quality Standards (NAAQS), so incense smoke can pose a health risk to people due to inhalation exposure of particulate matter. Emissions of carbon monoxide (CO), nitric oxide (NO), and sulfur dioxide (SO2) were also measured for seven types of incense. Emission rates of the gaseous pollutants were sufficient to cause indoor concentrations, estimated using the indoor air quality model, to exceed the outdoor concentrations specified by the NAAQS under certain conditions. However, the incense samples that were tested would fill a room with thick smoke under these conditions.
Risk Analysis | 2001
James J. Jetter; Reynaldo Forte; Reva Rubenstein
A fault tree analysis was used to estimate the number of refrigerant exposures of automotive service technicians and vehicle occupants in the United States. Exposures of service technicians can occur when service equipment or automotive air-conditioning systems leak during servicing. The number of refrigerant exposures of service technicians was estimated to be 135,000 per year. Exposures of vehicle occupants can occur when refrigerant enters passenger compartments due to sudden leaks in air-conditioning systems, leaks following servicing, or leaks caused by collisions. The total number of exposures of vehicle occupants was estimated to be 3,600 per year. The largest number of exposures of vehicle occupants was estimated for leaks caused by collisions, and the second largest number of exposures was estimated for leaks following servicing. Estimates used in the fault tree analysis were based on a survey of automotive air-conditioning service shops, the best available data from the literature, and the engineering judgement of the authors and expert reviewers from the Society of Automotive Engineers Interior Climate Control Standards Committee. Exposure concentrations and durations were estimated and compared with toxicity data for refrigerants currently used in automotive air conditioners. Uncertainty was high for the estimated numbers of exposures, exposure concentrations, and exposure durations. Uncertainty could be reduced in the future by conducting more extensive surveys, measurements of refrigerant concentrations, and exposure monitoring. Nevertheless, the analysis indicated that the risk of exposure of service technicians and vehicle occupants is significant, and it is recommended that no refrigerant that is substantially more toxic than currently available substitutes be accepted for use in vehicle air-conditioning systems, absent a means of mitigating exposure.
Environmental Science & Technology | 2018
Guofeng Shen; Michael D. Hays; Kirk R. Smith; Craig Williams; Jerroll W. Faircloth; James J. Jetter
Liquefied petroleum gas (LPG) cookstoves are considered to be an important solution for mitigating household air pollution; however, their performance has rarely been evaluated. To fill the data and knowledge gaps in this important area, 89 laboratory tests were conducted to quantify efficiencies and pollutant emissions from five commercially available household LPG stoves under different burning conditions. The mean thermal efficiency (±standard deviation) for the tested LPG cookstoves was 51 ± 6%, meeting guidelines for the highest tier level (Tier 4) under the International Organization for Standardization, International Workshop Agreement 11. Emission factors of CO2, CO, THC, CH4, and NOx on the basis of useful energy delivered (MJd) were 142 ± 17, 0.77 ± 0.55, 130 ± 196, 5.6 ± 8.2, and 46 ± 9 mg/MJd, respectively. Approximately 90% of the PM2.5 data were below the detection limit, corresponding to an emission rate below 0.11 mg/min. For those data above the detection limit, the average emission factor was 2.4 ± 1.6 mg/MJd, with a mean emission rate of 0.20 ± 0.16 mg/min. Under the specified gas pressure (2.8 kPa), but with the burner control set to minimum air flow rate, less complete combustion resulted in a visually yellow flame, and CO, PM2.5, EC, and BC emissions all increased. LPG cookstoves met guidelines for Tier 4 for both CO and PM2.5 emissions and mostly met the World Health Organization Emission Rate Targets set to protect human health.
Environmental Science & Technology | 2017
Guofeng Shen; Chethan K. Gaddam; Seth M. Ebersviller; Randy L. Vander Wal; Craig Williams; Jerroll W. Faircloth; James J. Jetter; Michael D. Hays
Ultrafine particle (UFP) emissions and particle number size distributions (PNSD) are critical in the evaluation of air pollution impacts; however, data on UFP number emissions from cookstoves, which are a major source of many pollutants, are limited. In this study, 11 fuel-stove combinations covering a variety of fuels and different stoves are investigated for UFP emissions and PNSD. The combustion of LPG and alcohol (∼1011 particles per useful energy delivered, particles/MJd), and kerosene (∼1013 particles/MJd), produced emissions that were lower by 2-3 orders of magnitude than solid fuels (1014-1015 particles/MJd). Three different PNSD types-unimodal distributions with peaks ∼30-40 nm, unimodal distributions with peaks <30 nm, and bimodal distributions-were observed as the result of both fuel and stove effects. The fractions of particles smaller than 30 nm (F30) varied among the tested systems, ranging from 13% to 88%. The burning of LPG and alcohol had the lowest PM2.5 mass emissions, UFP number emissions, and F30 (13-21% for LPG and 35-41% for alcohol). Emissions of PM2.5 and UFP from kerosene were also low compared with solid fuel burning but had a relatively high F30 value of approximately 73-80%.
Energy & Fuels | 2017
Guofeng Shen; William Preston; Seth M. Ebersviller; Craig Williams; Jerroll W. Faircloth; James J. Jetter; Michael D. Hays
This study measures polycyclic aromatic hydrocarbon (PAH) compositions in particulate matter emissions from residential cookstoves. A variety of fuel and cookstove combinations are investigated, including: (i) liquid petroleum gas (LPG), (ii) kerosene in a wick stove, (iii) wood (10 and 30% moisture content on a wet basis) in a forced-draft fan stove, and (iv) wood in a natural-draft rocket cookstove. The wood burning in the natural-draft stove had the highest PAH emissions followed by the wood combustion in the forced-draft stove and kerosene burning. LPG combustion has the highest thermal efficiency (∼57%) and the lowest PAH emissions per unit fuel energy, resulting in the lowest PAH emissions per useful energy delivered (in the unit of megajoule delivered, MJd). Compared with the wood combustion emissions, LPG burning also emits a lower fraction of higher molecular weight PAHs. In rural regions where LPG and kerosene are unavailable or unaffordable, the forced-draft fan stove is expected to be an alternative because its benzo[a]pyrene (B[a]P) emission factor (5.17-8.24 μg B[a]P/MJd) and emission rate (0.522-0.583 μg B[a]P/min) are similar to those of kerosene burning (5.36 μg B[a]P/MJd and 0.452 μg B[a]P/min). Relatively large PAH emission variability for LPG suggests a need for additional future tests to identify the major factors influencing these combustion emissions. These future tests should also account for different LPG fuel formulations and stove burner types.
Science of The Total Environment | 2009
Steven C. Patch; Margaret C. Ullman; Richard P. Maas; James J. Jetter
A controlled simulation experiment was performed to assess whether dislodgeable arsenic can be tracked onto carpets via foot traffic from chromated copper arsenate (CCA) pressure-treated decks. The pilot simulation study demonstrated that it is possible to track arsenic from CCA-decks onto carpets under the test conditions evaluated. A total of nine CCA-decks and two non-CCA-treated control surfaces were tested under wet and dry conditions. Five participants walked in a controlled manner (60 cycles, 11 steps per cycle) across decks and then walked over various lanes of carpet to simulate the tracking of arsenic indoors on the bottoms of shoes under heavy foot traffic conditions. To determine if arsenic was transferred from the CCA-treated wood to the carpet via shoes, laboratory analysis was performed on three different types of samples: (1) wipe samples of dislodgeable arsenic from a 46 cm(2) area of carpet, (2) dust samples obtained from vacuuming a 7442 cm(2) area of carpet, and (3) extractions of 13 cm(2) carpet samples. Wipe samples were also taken directly from the deck lumber. Following digestion and extraction, the amount of arsenic in each sample was measured using Graphite Furnace Atomic Absorption Spectrometry. The mean arsenic concentration measured on the carpets was 2.52 microg/(100 cm(2)) and 2.05 microg/(100 cm(2)) with wipes for the dry and wet conditions, respectively, 4.69 microg/(100 cm(2)) and 0.68 microg/(100 cm(2)) with vacuumed dust for the dry and wet conditions, respectively, and 15.56 microg/(100 cm(2)) and 12.31 microg/(100 cm(2)) with carpet extractions for the dry and wet conditions, respectively. The mean arsenic concentration measured on the decks was 22.2 microg/(100 cm(2)) with wipes. Further research is needed to determine if indoor exposure to arsenic due to track-in from outdoor decks via foot traffic is significant compared to exposures from other sources.
Environmental Pollution | 2018
Wei Du; Xi Zhu; Yuanchen Chen; Weijian Liu; Wei Wang; Guofeng Shen; Shu Tao; James J. Jetter
Residential combustion emission contributes significantly to ambient and indoor air pollution in China; however, this pollution source is poorly characterized and often overlooked in national pollution control policies. Few studies, and even fewer field-based investigations, have evaluated pollutant emissions from indoor biomass burning. One significant feature of Chinese household biofuel stoves is that many are built on site. In this study, 112 tests were conducted to investigate pollutant emission factors and variations for 11 fuel-stove combinations in actual use in the field. Results showed that, compared to those emission tests under controlled fuel burning conditions, EFs of methane, sulfur dioxide, particulate matter, and organic carbon from the field-based uncontrolled tests were higher, but carbon monoxide, nitrogen oxides, and elemental carbon were not significantly different. Controlled burning tests may be unrepresentative of real-world fuel burning. Pollutant emissions from uncontrolled burning tests had much higher variations compared with controlled tests. Most pollutant emissions from indoor straw burning are higher than that in open burning, except nitrogen oxides. The typical built-in-place home stoves in China had low efficiencies and high pollutant emissions that were rated as Tier 0 (the worst) or Tier 1 of a four-tier scale according to the International Organization for Standardization, International Workshop Agreement 11-2012. Effective interventions are expected to lower pollutant emissions from residential combustion to improve air quality and to protect human health.
Environmental Pollution | 2018
Mingjie Xie; Guofeng Shen; Amara L. Holder; Michael D. Hays; James J. Jetter
Household cookstove emissions are an important source of carbonaceous aerosols globally. The light-absorbing organic carbon (OC), also termed brown carbon (BrC), from cookstove emissions can impact the Earths radiative balance, but is rarely investigated. In this work, PM2.5 filter samples were collected during combustion experiments with red oak wood, charcoal, and kerosene in a variety of cookstoves mainly at two water boiling test phases (cold start CS, hot start HS). Samples were extracted in methanol and extracts were examined using spectrophotometry. The mass absorption coefficients (MACλ, m2 g-1) at five wavelengths (365, 400, 450, 500, and 550 nm) were mostly inter-correlated and were used as a measurement proxy for BrC. The MAC365 for red oak combustion during the CS phase correlated strongly to the elemental carbon (EC)/OC mass ratio, indicating a dependency of BrC absorption on burn conditions. The emissions from cookstoves burning red oak have an average MACλ 2-6 times greater than those burning charcoal and kerosene, and around 3-4 times greater than that from biomass burning measured in previous studies. These results suggest that residential cookstove emissions could contribute largely to ambient BrC, and the simulation of BrC radiative forcing in climate models for biofuel combustion in cookstoves should be treated specifically and separated from open biomass burning.
Archive | 2011
Robert Thompson; James J. Jetter; D. R. Marr; Clyde Owens
Addressing building energy use is the critical first step in any strategic plan for mitigating climate change. Buildings have a direct impact on estimated global climate change due to their large carbon footprint. Energy use in the building sector is the largest man-made contributor to climate change, and coincidentally a key sector to start mitigating climate change. To avoid revisiting problems such as sick building syndrome arising from aggressive building weatherization programs in the 1970s, it is critical that policy makers, regulators, and strategic planners remember that the primary function of buildings is not saving energy. The bottom line of why we build buildings is for safety and comfort in our homes, to enhance productivity in the workplace, and to ensure an optimal learning environment in our schools. The fundamental services of improving human health, comfort, productivity, and performance should not be compromised as we strive to minimize energy use in buildings. A one-dimensional focus on energy could result in unsustainable policies and practices. Much is understood about technologies, materials, and design techniques that can reduce energy use in buildings. However, much attention must be paid to recognizing how these approaches can enhance or damage human health and productivity as well as the environment. The focus of this chapter is not existing energy sectors and conservation technologies that have been extensively understood and considered in the literature, but on underutilized mitigation techniques that both increase the sustainability of our buildings while maintaining a focus on human health and the environment. A key intersection between climate change, buildings, and human health is building materials and products, and an effective testing and information transfer program is urgently needed so that building stakeholders have the information and tools they need to make good decisions during the design, construction, operation, and renovation phases of buildings.