The calibration and deployment of a low-cost methane sensor

被引:26
|
作者
Riddick, Stuart N. [1 ,5 ]
Mauzerall, Denise L. [1 ,2 ]
Celia, Michael [1 ]
Allen, Grant [3 ]
Pitt, Joseph [3 ,6 ]
Kang, Mary [4 ]
Riddick, John C. [1 ]
机构
[1] Princeton Univ, Dept Civil & Environm Engn, Princeton, NJ 08544 USA
[2] Princeton Univ, Woodrow Wilson Sch Publ & Int Affairs, Princeton, NJ 08544 USA
[3] Univ Manchester, Ctr Atmospher Sci, Manchester M13 9PL, Lancs, England
[4] McGill Univ, Dept Civil Engn & Appl Mech, Montreal, PQ H3A 0C3, Canada
[5] Colorado State Univ, Energy Inst, Ft Collins, CO 80523 USA
[6] SUNY Stony Brook, Sch Marine & Atmospher Sci, Stony Brook, NY 11794 USA
基金
美国海洋和大气管理局;
关键词
Methane; Mixing ratio; Measurement; Inexpensive; Calibration; GREENHOUSE-GAS EMISSION; OIL;
D O I
10.1016/j.atmosenv.2020.117440
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Since 1850 the atmospheric mixing ratio of methane (CH4), a potent greenhouse gas, has doubled. This increase is directly linked to an escalation in emissions from anthropogenic sources. An inexpensive means to identify and monitor CH4 emission sources and evaluate the efficacy of mitigation strategies is essential. However, sourcing reliable, low-cost, easy-to-calibrate sensors that are fit for purpose is challenging. A recent study showed that CH4 mixing ratio data from a low-power, low-cost CH4 sensor (Figaro TG52600) agreed well with CH4 mixing ratios measured by a high precision sensor at mixing ratios between 1.85 ppm and 2 ppm. To investigate, as a proof of concept, if this low-cost sensor could be used to measure typical ambient CH4 mixing ratios, we operated a TG52600 in conjunction with a Los Gatos Ultra-portable Greenhouse Gas Analyzer (UGGA) in controlled laboratory conditions. We then explored the sensor's long-term reliability by deploying the TG52600 near an onshore gas terminal to calculate emissions from May to July 2018. Our initial studies showed that previously published linear algorithms could not convert TG52600 output to CH4 mixing ratios measured by the UGGA. However, we derived a non-linear empirical relationship that could be used to reliably convert the output of a TG52600 unit to CH4 mixing ratios over a range of 1.85-5.85 ppm that agree to a high-precision instrument output to +/- 0.01 ppm. Our study showed that the TG52600 could be used to continuously measure variability in CH4 mixing ratios from 1.82 to 5.40 ppm for three months downwind of the gas terminal. Using a simplified Gaussian Plume approach, these mixing ratios correspond to an emission flux range of 0-238 g CH(4)s(-1), with average emission of 9.6 g CH(4)s(-1) from the currently active North Terminal and 1.6 g CH(4)s(-1) from the decommissioned South Terminal. Our work here demonstrates the feasibility of utilizing a low-cost sensor to detect methane leakage at concentrations close to ambient background levels, as long as the device is routinely calibrated with an accurate reference instrument. Having a widely deployed network of such low-cost CH4 sensors would allow improved identification, monitoring and mitigation of a variety of CH4 emissions.
引用
收藏
页数:7
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