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Effect of carbonation on the leaching of organic carbon and of copper from MSWI bottom ash

机译:碳酸化对MSWI底灰浸出有机碳和铜的影响

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摘要

In Flanders, the northern part of Belgium, about 31% of the produced amount of MSWI bottom ash is recycled as secondary raw material. In view of recycling a higher percentage of bottom ash, a particular bottom ash fraction (0 0.1-2 mm) was studied. As the leaching of this bottom ash fraction exceeds some of the Flemish limit values for heavy metals (with Cu being the most critical), treatment is required. Natural weathering and accelerated carbonation resulted in a significant decrease of the Cu leaching. Natural weathering during 3 months caused a decrease of Cu leaching to <50% of its original value, whereas accelerated carbonation resulted in an even larger decrease (to ca. 13% of its initial value) after 2 weeks, with the main decrease taking place within the first 48 h. Total organic carbon decreased to ca. 70% and 55% of the initial concentration in the solid phase, and to 40% and 25% in the leachate after natural weathering and after accelerated carbonation, respectively. In the solid material the decrease of the Hy fraction was the largest, the FA concentration remained essentially constant. The decrease of FA in the leachate can be attributed partly to an enhanced adsorption of FA to Fe/Al (hydr)oxides, due to the combined effect of a pH decrease and the neoformation of Al (hydroxides (both due to carbonation). A detailed study of adsorption of FA to Fe/Al (hydr)oxides showed that significant adsorption of FA occurs, that it increases with decreasing pH and started above pH 12 for Fe (hydr)oxides and around 10 for Al (hydr)oxides. Depending whether FA or Hy are considered the controlling factor in enhanced Cu leaching, the decreasing FA or Hy in the leachate explains the decrease in the Cu leaching during carbonation.
机译:在比利时北部的法兰德斯,大约31%的MSWI底灰产生量被回收用作辅助原料。考虑到回收更高百分比的底灰,研究了特定的底灰分率(0 0.1-2 mm)。由于这种底灰分的浸出超过了重金属的某些弗拉芒极限值(其中Cu是最关键的),因此需要进行处理。自然风化和加速碳化导致铜的浸出显着减少。 3个月的自然风化使铜的浸出量减少到其原始值的<50%,而加速的碳酸化作用导致2周后的浸出量甚至更大(下降至其初始值的约13%),主要发生在在最初的48小时内。总有机碳减少到大约固相中初始浓度的70%和55%,以及自然风化后和加速碳化后分别在渗滤液中达到40%和25%。在固体材料中,Hy分数的下降最大,FA浓度基本保持恒定。由于pH值降低和Al(氢氧化物(均由于碳化)而新形成)的综合作用,渗滤液中FA的减少可部分归因于FA对Fe / Al(氢)氧化物的吸附增强。对FA在Fe / Al(氢)氧化物上的吸附的详细研究表明,FA发生了显着的吸附,随着pH的降低,FA的吸附增加,对于Fe(氢)氧化物,其开始于pH高于12,对于Al(氢)氧化物,其约为10左右。不管FA或Hy被认为是增加Cu浸出的控制因素,渗滤液中FA或Hy的减少都说明了碳化过程中Cu浸出的减少。

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  • 来源
    《Waste Management》 |2010年第7期|1296-1302|共7页
  • 作者单位

    KHLeuven, Department of Health and Technology, Herestraat 49,3000 Leuven, Belgium;

    Department of Chemical Engineering, K.U. Leuven, de Croylaan 46, B-3001 Leuven, Belgium;

    Department of Chemical Engineering, K.U. Leuven, de Croylaan 46, B-3001 Leuven, Belgium;

    Department of Chemical Engineering, K.U. Leuven, de Croylaan 46, B-3001 Leuven, Belgium;

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