Evaluation of a biologically active cover for mitigation of landfill gas emissions

被引:178
作者
Barlaz, MA
Green, RB
Chanton, JP
Goldsmith, CD
Hater, GR
机构
[1] N Carolina State Univ, Dept Civil Construct & Environm Engn, Raleigh, NC 27695 USA
[2] Waste Management Inc, Bioreactor & BioSites Technol, Cincinnati, OH 45211 USA
[3] Florida State Univ, Dept Oceanog, Tallahassee, FL 32306 USA
[4] Alternat Nat Technol Inc, Blacksburg, VA 24060 USA
关键词
D O I
10.1021/es049605b
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Landfills are the third largest source of anthropogenic CH4 in the United States, and there is potential for reduction in this source of greenhouse gases and other contaminants. The objective of this work was to contrast emissions of CH4 and non-methane organic compounds (NMOGs) from landfill cells covered with soil or a biologically active cover consisting of yard waste compost. On the basis of four field campaigns over 14 months, CH4 emissions from the biocover (BC) varied from -1.73 to 1.33 g m(-2) d(-1), with atmospheric uptake measured in 52% of tests. BC emissions did not increase when the gas collection system was turned off. Uptake of atmospheric CH4 was measured in 54% of tests on the soil cover (SC) when the gas collection was system active and 12% when the gas collection system was off. Many (26%) relatively high fluxes (>15 g m(-2) d(-1)) were measured from the SIC as were some dramatic effects due to deactivation of the gas collection system. In tests with positive emissions, stable isotope measurements showed that the BC and SC were responsible for oxidation of 55% and 21% of the CH4 reaching the bottom of the respective cover. Seven of the highest 10 NMOC emissions were measured in the SC, and 17 of 21 fluxes for speciated organic compounds were higher in the SC. The relationship between CH4, NMOC, and individual organic compound emissions suggested a correlation between CH4 and trace organic oxidation. BCs can reduce landfill gas emissions in the absence of a gas collection system and can serve as a polishing step in the presence of an active system.
引用
收藏
页码:4891 / 4899
页数:9
相关论文
共 41 条
[1]   Trace organic compounds in landfill gas at seven UK waste disposal sites [J].
Allen, MR ;
Braithwaite, A ;
Hills, CC .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1997, 31 (04) :1054-1061
[2]  
[Anonymous], ADVAN AT MOL PHYS
[3]   CARBON ISOTOPE FRACTIONATION DURING MICROBIAL METHANE OXIDATION [J].
BARKER, JF ;
FRITZ, P .
NATURE, 1981, 293 (5830) :289-291
[4]   Stable isotopic signatures (δ13C, δD) of methane from European landfill sites [J].
Bergamaschi, P ;
Lubina, C ;
Konigstedt, R ;
Fischer, H ;
Veltkamp, AC ;
Zwaagstra, O .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1998, 103 (D7) :8251-8265
[5]   Methane emission from a landfill and the methane oxidising capacity of its covering soil [J].
Boeckx, P ;
vanCleemput, O ;
Villaralvo, I .
SOIL BIOLOGY & BIOCHEMISTRY, 1996, 28 (10-11) :1397-1405
[6]   Kinetics of methane oxidation in a landfill cover soil: Temporal variations, a whole landfill oxidation experiment, and modeling of net CH4 emissions [J].
Bogner, JE ;
Spokas, KA ;
Burton, EA .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1997, 31 (09) :2504-2514
[7]  
Bradley Paul M., 2003, Bioremediation Journal, V7, P81, DOI 10.1080/713607980
[8]   Seasonal variation in methane oxidation in a landfill cover soil as determined by an in situ stable isotope technique [J].
Chanton, J ;
Liptay, K .
GLOBAL BIOGEOCHEMICAL CYCLES, 2000, 14 (01) :51-60
[9]   Quantifying methane oxidation from landfills using stable isotope analysis of downwind plumes [J].
Chanton, JP ;
Rutkowski, CM ;
Mosher, B .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1999, 33 (21) :3755-3760
[10]   FRACTIONATION OF CARBON AND HYDROGEN ISOTOPES BY METHANE-OXIDIZING BACTERIA [J].
COLEMAN, DD ;
RISATTI, JB ;
SCHOELL, M .
GEOCHIMICA ET COSMOCHIMICA ACTA, 1981, 45 (07) :1033-1037