Community Air Sensor Network (CAIRSENSE) project: evaluation of low-cost sensor performance in a suburban environment in the southeastern United States

被引:329
作者
Jiao, Wan [1 ]
Hagler, Gayle [1 ]
Williams, Ronald [1 ]
Sharpe, Robert [2 ]
Brown, Ryan [3 ]
Garver, Daniel [3 ]
Judge, Robert [4 ]
Caudill, Motria [5 ]
Rickard, Joshua [6 ]
Davis, Michael [7 ]
Weinstock, Lewis [8 ]
Zimmer-Dauphinee, Susan [9 ]
Buckley, Ken [9 ]
机构
[1] US EPA, Off Res & Dev, Res Triangle Pk, NC 27711 USA
[2] ARCADIS US Inc, Durham, NC 27713 USA
[3] US EPA, Reg 4, Atlanta, GA 30303 USA
[4] US EPA, Reg 1, Boston, MA 02109 USA
[5] US EPA, Reg 5, Chicago, IL 60604 USA
[6] US EPA, Reg 8, Denver, CO 80202 USA
[7] US EPA, Reg 7, Lenexa, KS 66219 USA
[8] US EPA, Off Air Qual Planning & Stand, Res Triangle Pk, NC 27711 USA
[9] Georgia Environm Protect Div, Atlanta, GA 30354 USA
关键词
DENSITY NETWORKS; NITROGEN-DIOXIDE; POLLUTION; QUALITY;
D O I
10.5194/amt-9-5281-2016
中图分类号
P4 [大气科学(气象学)];
学科分类号
0706 ; 070601 ;
摘要
Advances in air pollution sensor technology have enabled the development of small and low-cost systems to measure outdoor air pollution. The deployment of a large number of sensors across a small geographic area would have potential benefits to supplement traditional monitoring networks with additional geographic and temporal measurement resolution, if the data quality were sufficient. To understand the capability of emerging air sensor technology, the Community Air Sensor Network (CAIRSENSE) project deployed low-cost, continuous, and commercially available air pollution sensors at a regulatory air monitoring site and as a local sensor network over a surrounding similar to 2 km area in the southeastern United States. Collocation of sensors measuring oxides of nitrogen, ozone, carbon monoxide, sulfur dioxide, and particles revealed highly variable performance, both in terms of comparison to a reference monitor as well as the degree to which multiple identical sensors produced the same signal. Multiple ozone, nitrogen dioxide, and carbon monoxide sensors revealed low to very high correlation with a reference monitor, with Pearson sample correlation coefficient (r) ranging from 0.39 to 0.97, 0.25 to 0.76, and 0.40 to 0.82, respectively. The only sulfur dioxide sensor tested revealed no correlation (r < 0.5) with a reference monitor and erroneously high concentration values. A wide variety of particulate matter (PM) sensors were tested with variable results - some sensors had very high agreement (e.g., r = 0.99) between identical sensors but moderate agreement with a reference PM2.5 monitor (e.g., r = 0.65). For select sensors that had moderate to strong correlation with reference monitors (r > 0.5), step-wise multiple linear regression was performed to determine if ambient temperature, relative humidity (RH), or age of the sensor in number of sampling days could be used in a correction algorithm to improve the agreement. Maximum improvement in agreement with a reference, incorporating all factors, was observed for an NO2 sensor (multiple correlation coefficient R-adj-orig(2) = 0.57, R-adj-final(2) = 0.81); however, other sensors showed no apparent improvement in agreement. A four-node sensor network was successfully able to capture ozone (two nodes) and PM (four nodes) data for an 8-month period of time and show expected diurnal concentration patterns, as well as potential ozone titration due to nearby traffic emissions. Overall, this study demonstrates the performance of emerging air quality sensor technologies in a real-world setting; the variable agreement between sensors and reference monitors indicates that in situ testing of sensors against benchmark monitors should be a critical aspect of all field studies.
引用
收藏
页码:5281 / 5292
页数:12
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