Lindberg S E, Price J L
a Oak Ridge National Laboratory (ORNL) , Environmental Sciences Division , Oak Ridge , Tennessee , USA.
b Florida Department of Environmental Protection , Waste Management Division , Tallahassee , Florida , USA.
J Air Waste Manag Assoc. 1999 May;49(5):520-532. doi: 10.1080/10473289.1999.10463825.
Large quantities of mercury (Hg) have been placed in municipal landfills from a wide array of sources, including fluorescent lights, batteries, electrical switches, thermometers, and general waste. Despite its known volatility, persistence, and toxicity in the environment, the fate of this Hg has not been widely studied. Using automated flux chambers and atmospheric sampling, we quantified the primary pathways of Hg vapor releases to the atmosphere at two municipal landfill operations in south Florida for eight days in April 1997. These pathways included landfill gas (LFG) releases from passive and active vent systems, passive emissions from landfill surface covers of different ages (including CH "hot spots"), and emissions from daily activities at a working face (WF). Hg vapor was released to the atmosphere at readily detectable rates from all sources measured. Emission rates ranged from ~1 to 20 ng m hr over aged surface covers (generally comparable to background soils), from ~6 to 2400 ng/hr from LFG vents and flares, and from ~5 to 60 mg/hr at the WF. In general the fluxes increased from older to newer landfills, from fresh to aged cover, and from passive to active venting systems. Limited data suggest that methyl- and other organo-mercury compounds may also be emitted from these sites, suggesting an important area for future research. We estimate that atmospheric Hg releases from municipal landfill operations in the state of Florida are on the order of 10 kg/yr, or <1% of the estimated total anthropogenic Hg releases to air in this region.
大量汞(Hg)通过多种来源被排放到城市垃圾填埋场,这些来源包括荧光灯、电池、电气开关、温度计以及一般垃圾。尽管汞在环境中具有挥发性、持久性和毒性已为人所知,但其在垃圾填埋场中的归宿尚未得到广泛研究。我们于1997年4月在佛罗里达州南部的两个城市垃圾填埋场,使用自动通量室和大气采样方法,对汞蒸气释放到大气中的主要途径进行了为期八天的量化研究。这些途径包括来自被动和主动通风系统的填埋气(LFG)排放、不同年份填埋场表面覆盖物(包括CH“热点”)的被动排放以及作业面(WF)日常活动的排放。在所测量的所有来源中,汞蒸气均以易于检测到的速率释放到大气中。排放速率范围为:在老化的表面覆盖物上约为1至20纳克/平方米·小时(通常与背景土壤相当),从LFG通风口和火炬处约为6至2400纳克/小时,在作业面约为5至60微克/小时。一般来说,通量从较旧的填埋场到较新的填埋场、从新鲜覆盖物到老化覆盖物、从被动通风系统到主动通风系统逐渐增加。有限的数据表明,甲基汞和其他有机汞化合物也可能从这些地点排放,这表明这是未来研究的一个重要领域。我们估计,佛罗里达州城市垃圾填埋场作业向大气中释放的汞约为10千克/年,占该地区估计人为汞排放总量的不到1%。