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从受污染土壤中同时去除多氯二苯并二恶英/多氯二苯并呋喃、五氯苯酚和汞。

Simultaneous removal of PCDD/Fs, pentachlorophenol and mercury from contaminated soil.

作者信息

Hung Pao-Chen, Chang Shu-Hao, Ou-Yang Chia-Chien, Chang Moo-Been

机构信息

Graduate Institute of Environmental Engineering, National Central University, Chungli 320, Taiwan.

Graduate Institute of Environmental Engineering, National Central University, Chungli 320, Taiwan.

出版信息

Chemosphere. 2016 Feb;144:50-8. doi: 10.1016/j.chemosphere.2015.08.058. Epub 2015 Sep 5.

Abstract

Pentachlorophenol (PCP), polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs), and mercury were simultaneously removed from heavily contaminated soil using a continuous pilot-scale thermal system (CPTS). Operating the system at 700 °C with 22 min of retention time ensured that the residual contaminants in remediated soil are lower in concentration than the soil standards of Taiwan EPA require. Both PCP and PCDD/Fs are effectively destroyed during the treatment at high temperatures in the CPTS, but significant dechlorination of PCDD/Fs is also found, resulting in lower net destruction efficiencies of TCDD/F and PeCDD/F-congeners, compared with those of highly chlorinated Hx-, Hp- and OCDD/F congeners. Moreover, 2,3,7,8-TetraCDD is significantly formed if the retention time is not long enough for total destruction. Inadequate reaction time (or retention time) even may lead to a rise in TEQ-value due to incomplete dechlorination. Mercury is significantly desorbed from contaminated soil and discharged through the exhaust. For PCP and PCDD/Fs, the exhaust discharge percentages including both the remediated soil and the exhaust are <0.03% and 1.14% of the input, respectively, achieved with 700 °C and 33 min retention time. In contrast, some 97.8% of input mercury rate is desorbed and discharged via the exhaust, so that the latter should be carefully cleaned via efficient air pollution control devices, whereas this contribution focuses on the conditions required for reaching adequate soil cleaning.

摘要

使用连续中试规模热系统(CPTS)从重度污染土壤中同时去除五氯苯酚(PCP)、多氯二苯并 - 对 - 二恶英和二苯并呋喃(PCDD/Fs)以及汞。在700℃下运行该系统并保持22分钟的停留时间,可确保修复后土壤中的残留污染物浓度低于台湾环保署要求的土壤标准。PCP和PCDD/Fs在CPTS的高温处理过程中均被有效破坏,但也发现PCDD/Fs有显著的脱氯现象,与高氯代的六氯代二恶英/呋喃(Hx - OCDD/F)、七氯代二恶英/呋喃(Hp - OCDD/F)和八氯代二恶英/呋喃(OCDD/F)同系物相比,导致四氯代二恶英/呋喃(TCDD/F)和五氯代二恶英/呋喃(PeCDD/F)同系物的净破坏效率较低。此外,如果停留时间不足以实现完全破坏,会显著生成2,3,7,8 - 四氯二苯并二恶英(2,3,7,8 - TetraCDD)。反应时间(或停留时间)不足甚至可能由于脱氯不完全导致毒性当量(TEQ)值升高。汞从污染土壤中显著解吸并通过废气排放。对于PCP和PCDD/Fs,在700℃和33分钟停留时间的条件下,包括修复后土壤和废气中的排放百分比分别<输入量的0.03%和1.14%。相比之下,约97.8%的输入汞率通过废气解吸并排放,因此废气应通过高效的空气污染控制装置仔细净化,而本研究重点关注实现充分土壤净化所需的条件。

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