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热解四溴双酚 A 过程中氧化铅的命运。

Fate of lead oxide during thermal treatment with tetrabromobisphenol A.

机构信息

Institute of Multidisciplinary Research for Advanced Materials (IMRAM), Tohoku University, 1,1 Katahira, 2-Chome, Aoba-ku, Sendai 980-8577, Japan; Institute of Environmental Engineering of the Polish Academy of Sciences, M. Sklodowska-Curie 34, 41-819 Zabrze, Poland.

出版信息

J Hazard Mater. 2013 Oct 15;261:163-71. doi: 10.1016/j.jhazmat.2013.07.028. Epub 2013 Jul 22.

Abstract

In this paper, the bromination reaction between lead oxide and hydrogen bromide originating from the thermal decomposition of tetrabromobisphenol A (TBBPA), under inert and oxidizing atmospheres, was investigated, using a laboratory-scale furnace. The results obtained under inert conditions indicated that bromination of PbO proceeded simultaneously with debromination of TBBPA, with an average effectiveness of 69% (max. 80%). Volatilization of the formed PbBr2 began at 315°C, intensified at 750°C, and reached 98% at 850°C. The formed organic char served as a source of carbon for reduction of the unreacted lead oxide to metallic lead in the range 315-750°C. Additional experiments conducted at selected temperatures under slightly oxidizing (5 vol% O2) and quasi-atmospheric (20 vol% O2) conditions showed no significant effects on bromination-evaporation of lead in the studied mixture. However, in isothermal treatment under quasi-atmospheric oxygen levels, complete vaporization of the formed lead bromide was obtained at a temperature of only 650°C.

摘要

本文研究了在惰性和氧化气氛下,由四溴双酚 A(TBBPA)热分解产生的氧化铅与氢溴酸之间的溴化反应,使用实验室规模的炉。在惰性条件下得到的结果表明,PbO 的溴化反应与 TBBPA 的脱溴反应同时进行,平均效率为 69%(最高 80%)。形成的 PbBr2 于 315°C 开始挥发,在 750°C 时加剧,并在 850°C 时达到 98%。形成的有机炭质作为碳源,将未反应的氧化铅还原为金属铅,反应温度范围为 315-750°C。在选定温度下进行的其他实验,在轻微氧化(5 vol% O2)和准大气(20 vol% O2)条件下进行,表明对研究混合物中铅的溴化-蒸发没有显著影响。然而,在准大气氧气水平下的等温处理中,仅在 650°C 即可获得形成的溴化铅的完全蒸发。

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