State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences , Beijing 100085, China.
Toxicology & Environmental Research and Consulting (TERC), The Dow Chemical Company , Midland, Michigan 48674, United States.
Environ Sci Technol. 2017 Nov 7;51(21):12337-12346. doi: 10.1021/acs.est.7b03624. Epub 2017 Oct 12.
In one yearly cycle (2016), D4 and D5 were detected in biogas samples (n = 36, 0.105-2.33 mg/m) from a Chinese municipal landfill, while D4-D6 were detected in influents/effluents of leachate storage pond (n = 72, < LOQ-30.5 μg/L). Mass loads of cVMS in both biogas (591-6575 mg/d) and leachate influents (659-5760 mg/d) increased from January to July (summer), and then decreased from July to December (winter). Removal experiments indicated that 1) hydrolysis and volatilization were predominant removal mechanism for D4 and D5, respectively, in leachate storage pond, responsible for their more significant removal (94.5-100%) in August; 2) indirect phototransformation (t = 25.5-87.0 days), such as hydroxylation by OH radical generated in leachates, was the predominant (50.0-75.5%) removal pathway for D6, which led to the largest removal efficiencies (65.2-73.7%) in June, the month with the largest sun light intensity and highest photosensitizer (e.g., Fe and NO) concentrations. Monohydroxylated products of D5 and D6, D4TOH and D5TOH, were detected in leachate effluents (39.6-187 ng/L) during May-July. Compared to D5 and D6, volatilization half-lives of D4TOH (86.3 days) and D5TOH (177 days) in leachates were 2.9 and 1.4 times longer, while their hydrolysis half-lives (7.50 days for D4TOH and 21.5 days for D5TOH) were 7.1 and 10 times shorter, respectively.
在一个年度周期(2016 年)中,在中国城市垃圾填埋场的沼气样本(n=36,0.105-2.33mg/m)中检测到 D4 和 D5,而在渗滤液储存池的进水/出水(n=72,<LOQ-30.5μg/L)中检测到 D4-D6。沼气(591-6575mg/d)和渗滤液进水(659-5760mg/d)中 cVMS 的质量负荷从 1 月到 7 月(夏季)增加,然后从 7 月到 12 月(冬季)减少。去除实验表明,1)水解和挥发分别是渗滤液储存池D4 和 D5 的主要去除机制,导致它们在 8 月去除率更高(94.5-100%);2)间接光转化(t=25.5-87.0 天),如由渗滤液中生成的 OH 自由基引起的羟化,是 D6 的主要(50.0-75.5%)去除途径,导致 6 月去除效率最高(65.2-73.7%),该月光照强度最大,敏化剂(如 Fe 和 NO)浓度最高。在 5 月至 7 月期间,在渗滤液废水中检测到 D5 和 D6 的单羟基化产物 D4TOH 和 D5TOH(39.6-187ng/L)。与 D5 和 D6 相比,D4TOH(86.3 天)和 D5TOH(177 天)在渗滤液中的挥发半衰期分别长 2.9 和 1.4 倍,而水解半衰期(D4TOH 为 7.50 天,D5TOH 为 21.5 天)分别短 7.1 和 10 倍。