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1.
Environ Sci Technol ; 52(21): 12915-12925, 2018 11 06.
Article in English | MEDLINE | ID: mdl-30256618

ABSTRACT

We used site-level methane (CH4) emissions data from over 1000 natural gas (NG) production sites in eight basins, including 92 new site-level CH4 measurements in the Uinta, northeastern Marcellus, and Denver-Julesburg basins, to investigate CH4 emissions characteristics and develop a new national CH4 emission estimate for the NG production sector. The distribution of site-level emissions is highly skewed, with the top 5% of sites accounting for 50% of cumulative emissions. High emitting sites are predominantly also high producing (>10 Mcfd). However, low NG production sites emit a larger fraction of their CH4 production. When combined with activity data, we predict that this creates substantial variability in the basin-level CH4 emissions which, as a fraction of basin-level CH4 production, range from 0.90% for the Appalachian and Greater Green River to >4.5% in the San Juan and San Joaquin. This suggests that much of the basin-level differences in production-normalized CH4 emissions reported by aircraft studies can be explained by differences in site size and distribution of site-level production rates. We estimate that NG production sites emit total CH4 emissions of 830 Mg/h (95% CI: 530-1200), 63% of which come from the sites producing <100 Mcfd that account for only 10% of total NG production. Our total CH4 emissions estimate is 2.3 times higher than the U.S. Environmental Protection Agency's estimate and likely attributable to the disproportionate influence of high emitting sites.


Subject(s)
Air Pollutants , Natural Gas , Appalachian Region , Methane , United States , United States Environmental Protection Agency
2.
Phys Rev Lett ; 108(20): 203201, 2012 May 18.
Article in English | MEDLINE | ID: mdl-23003146

ABSTRACT

Using cryogenic helium buffer-gas cooling, we have prepared dense samples of atomic lithium and molecular calcium monohydride at temperatures as low as 1 K. We have measured the Li+CaH→LiH+Ca chemical reaction, observed in both the accelerated disappearance of CaH in the presence of high densities of lithium and in the appearance of the LiH molecule.

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