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新型溴化二恶英和呋喃的合成。

De novo synthesis of brominated dioxins and furans.

机构信息

Chemical Engineering Department, University of Alicante , Post Office Box 99, 03080 Alicante, Spain.

出版信息

Environ Sci Technol. 2014 Jul 15;48(14):7959-65. doi: 10.1021/es501818d. Epub 2014 Jun 26.

Abstract

On the basis of laboratory experiments with model mixtures (active carbon+CuBr2 at different loads), this work studies the formation of polybrominated dibenzo-p-dioxins and dibenzofurans (PBDD/Fs) by de novo synthesis. For the different samples, the temperature of the maximum carbon oxidation rate was determined by thermogravimetric analysis, and a kinetic model was proposed for the degradation of the materials in an oxidizing atmosphere (synthetic air). The effect of the addition of different amounts of CuBr2 was studied, finding that its presence accelerates the degradation of the carbonaceous structure in the presence of oxygen. The thermal degradation of the samples in air is satisfactorily described by a first-order single-reaction model. In addition, combustion runs of one of the mixtures (consisting of activated carbon+50 wt % CuBr2, pyrolyzed at 700 °C) were performed in a quartz horizontal laboratory furnace. The analysis of the emissions and the solid residue proved the formation of brominated dioxins and furans at 300, 400, and 500 °C, with a maximum yield at 300 °C (91.7 ng/g of total PBDD/Fs) and a higher bromination degree with increasing temperature.

摘要

基于对模型混合物(不同负载量的活性炭+CuBr2)的实验室实验,本工作研究了从头合成法形成多溴二苯并二恶英和多溴二苯并呋喃(PBDD/Fs)的情况。通过热重分析确定了不同样品中最大碳氧化速率的温度,并提出了在氧化气氛(合成空气)中降解材料的动力学模型。研究了添加不同量 CuBr2 的效果,发现其存在会加速含氧条件下碳质结构的降解。空气样品的热降解可以用一级单反应模型很好地描述。此外,在石英水平实验室炉中进行了一种混合物(由在 700°C 下热解的活性炭+50wt%CuBr2 组成)的燃烧实验。排放物和固体残余物的分析证明,在 300、400 和 500°C 下形成了溴化二恶英和呋喃,在 300°C 时产率最高(总 PBDD/Fs 为 91.7ng/g),随着温度的升高,溴化程度也增加。

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