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271.
Novel aerial methane (CH4) detection technologies were used in this study to identify anomalously high-emitting oil and gas (O&G) facilities and to guide ground-based “leak detection and repair” (LDAR) teams. This approach has the potential to enable a rapid and effective inspection of O&G facilities under voluntary or regulatory LDAR programs to identify and mitigate anomalously large CH4 emissions from a disproportionately small number of facilities. This is the first study of which the authors are aware to deploy, evaluate, and compare the CH4 detection volumes and cost-effectiveness of aerially guided and purely ground-based LDAR techniques. Two aerial methods, the Kairos Aerospace infrared CH4 column imaging and the Scientific Aviation in situ aircraft CH4 mole fraction measurements, were tested during a 2-week period in the Fayetteville Shale region contemporaneously with conventional ground-based LDAR. We show that aerially guided LDAR can be at least as cost-effective as ground-based LDAR, but several variable parameters were identified that strongly affect cost-effectiveness and which require field research and improvements beyond this pilot study. These parameters include (i) CH4 minimum dectectable limit of aerial technologies, (ii) emission rate size distributions of sources, (iii) remote distinction of fixable versus nonfixable CH4 sources (“leaks” vs. CH4 emissions occurring by design), and (iv) the fraction of fixable sources to total CH4 emissions. Suggestions for future study design are provided.

Implications: Mitigation of methane leaks from existing oil and gas operations currently relies on on-site inspections of all applicable facilities at a prescribed frequency. This approach is labor- and cost-intensive, especially because a majority of oil and gas–related methane emissions originate from a disproportionately small number of facilities and components. We show for the first time in real-world conditions how aerial methane measurements can identify anomalously high-emitting facilities to enable a rapid, focused, and directed ground inspection of these facilities. The aerially guided approach can be more cost-effective than current practices, especially when implementing the aircraft deployment improvements discussed here.  相似文献   

272.
A method, based on XAD-8 resin sorbtion and Particle Induced X-ray Emission (PIXE), was developed for Total Organic Chlorine (TOCl) determinations. The method was applied to recipient waters of a kraft bleach plant, and the determined TOCl values compared with other parameters. The detection limit was about 10 μg/l.  相似文献   
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Amending poultry litter with Al sulfate (alum) has proven effective in reducing water-soluble P in the litter and in runoff from fields that have received litter applications. Although its effectiveness has been demonstrated on a macroscopic scale in the field or in the poultry houses, little is known about P speciation in either alum-amended or unamended litter. This knowledge is important for the evaluation of long-term stability and bioavailability of P, which is a necessary prerequisite for the assessment of the sustainability of intensive poultry operations. Here we report results from an investigation of alum-amended poultry litter (PL) that combined a chemical extraction sequence with solid-state 31P nuclear magnetic resonance (NMR) spectroscopic analysis of the residues. Aluminum is predominantly found in the fine size separate (<125 microm), indicating that the alum added to the poultry houses hydrolyzed without being completely dispersed in the litter. The NMR spectra confirmed the hypothesis that calcium phosphate phases are only dissolved during extraction with dilute acid and phosphate associated with Al is mainly dissolved during extraction with NaOH. Extraction of phosphate associated with Al was incomplete, however, as evidenced by 31P NMR spectroscopy. It could also be demonstrated that the extraction sequence overestimates the calcium phosphate fraction by an order of magnitude in this particular sample. Results from sequential chemical extraction should therefore be used with caution when assessing the magnitude of different phosphate pools in poultry litter.  相似文献   
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