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在固体废物焚烧过程中氧化钙抑制氯苯的形成。

Inhibition of chlorobenzenes formation by calcium oxide during solid waste incineration.

机构信息

State Key Laboratory of Pollution Control and Resource Reuse, Tongji University, Shanghai, 200092, China; Institute of Waste Treatment & Reclamation, College of Environmental Science and Engineering, Tongji University, Shanghai, 200092, China; Shanghai Institute of Pollution Control and Ecological Security, Shanghai, 200092, China.

State Key Laboratory of Pollution Control and Resource Reuse, Tongji University, Shanghai, 200092, China; Institute of Waste Treatment & Reclamation, College of Environmental Science and Engineering, Tongji University, Shanghai, 200092, China.

出版信息

J Hazard Mater. 2020 Dec 5;400:123321. doi: 10.1016/j.jhazmat.2020.123321. Epub 2020 Jun 26.

Abstract

Solid waste incineration is a major emission source of polychlorinated dibenzo-p-dioxins and polychlorinated dibenzofurans (PCDD/Fs). The injection of N- and S-containing compounds is an effective way to suppress the formation of PCDD/Fs, but this approach is still shortcoming because additional pollutants such as NH and SO are emitted. To avoid the secondary pollutions, a de novo synthesis inhibition mechanism in the presence of CaO was postulated to transform CuCl to CuO and deplete Cl and HCl. Chlorobenzenes (CBzs), which are indicators and precursors of PCDD/Fs, were adopted to prove the inhibitory effect of CaO at 400 °C, using both simulated synthetic ash and extracted air pollution control residues. As the molar ratio of CaO to CuCl exceeded 3, the residual carbon increased, and the inhibition efficiency of CBzs exceeded 93 %. This performance is superior to the corresponding performance of NHHPO, which has been proved to be a potential inhibitor. Furthermore, with CaO, chlorides remained in the solid phase and had inactive catalytic performance; and they were the major products rather than HCl, Cl and CuOCl. The addition of CaO during waste incineration therefore can facilitate the abatement of PCDD/Fs contamination and reduce the emissions of acid gas simultaneously.

摘要

固体废物焚烧是多氯二苯并对二恶英和多氯二苯并呋喃(PCDD/Fs)的主要排放源。 注入含 N 和 S 的化合物是抑制 PCDD/Fs 形成的有效方法,但这种方法仍有缺陷,因为会排放出额外的污染物,如 NH 和 SO。为了避免二次污染,提出了在 CaO 存在下的从头合成抑制机制,将 CuCl 转化为 CuO,并消耗 Cl 和 HCl。采用氯苯(CBzs)作为 PCDD/Fs 的指示物和前体,在 400°C 下使用模拟合成灰分和提取的空气污染控制残渣来证明 CaO 的抑制作用。当 CaO 与 CuCl 的摩尔比超过 3 时,残余碳增加,CBzs 的抑制效率超过 93%。这种性能优于已被证明是潜在抑制剂的 NHHPO 的相应性能。此外,在 CaO 存在下,氯留在固相,没有活性催化性能;它们是主要产物,而不是 HCl、Cl 和 CuOCl。因此,在废物焚烧过程中添加 CaO 可以促进 PCDD/Fs 污染的减少,并同时减少酸性气体的排放。

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