《Table 1–Quantification methods of Cl content in solid materials (Wang et al., 2010;Rahim et al., 20

《Table 1–Quantification methods of Cl content in solid materials (Wang et al., 2010;Rahim et al., 20   提示:宽带有限、当前游客访问压缩模式
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《Review on fate of chlorine during thermal processing of solid wastes》


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Several methods are available for determining Cl content in solid materials,which can be classified into four categories,i.e.,combustion,hydrolysis,extraction(Wang et al.,2010;Rahim et al.,2013b)and spectroscopy(Pereira et al.,2014)methods,as presented in Table 1.The combustion methods are the most commonly used methods,e.g.,bomb combustion(BC),flask combustion(FC),muffle/tube furnace combustion(MFC)and microwave-induced combustion(MIC).Combustion methods are capable to quantify the total Cl content(TCC)due to the high operating temperatures(>1000°C).Although Cl may still exist in the residues after combustion,the amount is negligible comparatively to the corresponding TCC(Silva et al.,2014).However,the non-volatile Cl in ash is not negligible by MFC at relatively lower temperatures(<1000°C),which can be further quantified by water washing(Ma et al.,2010)or spectroscopy analyses.Water washing methods are specially used for the determination of water-soluble Cl.The remained water-insoluble Cl in dried solid matters can be quantified by combustion methods.Digestion(acid and microwave)methods have the problem of analyte loss due to the formation of volatile Cl-compounds(Pereira et al.,2014).Spectroscopy methods can achieve non-destructive analyses on solid materials(Ne?emer et al.,2003),e.g.,X-ray fluorescence(XRF)and instrumental neutron activation analysis(INAA).The minimum detection limit of INAA is in the sub-ppm range with an accuracy in the region of 5%(Pollard and Heron,2008).However,non-destructive methods have very strict requirement on the homogeneity of solid sample.The choice of specific Cl quantification method depends on the species,content and distribution of Cl in solid materials.