Laboratory for Earth Surface Processes, College of Urban and Environmental Sciences, Peking University, Beijing 100871, PR China.
Laboratory for Earth Surface Processes, College of Urban and Environmental Sciences, Peking University, Beijing 100871, PR China.
J Hazard Mater. 2018 Jun 5;351:270-276. doi: 10.1016/j.jhazmat.2018.03.012. Epub 2018 Mar 9.
Two typical types of electronic waste (E-waste) were selected to investigate the emission characteristics of polycyclic aromatic hydrocarbons (PAHs) during pyrolytic processing, including emission factor, compositional profile, size distribution and gas-particle partitioning. The mean emission factors (EFs) of total PAHs were measured to be 2.77 ± 1.41 μg/g and 23.65 ± 14.52 μg/g for printed wiring boards and plastic casings, respectively, lower than those for coal combustion and biomass burning. Low molecular weight species were predominant in exhaust fumes, with overwhelming amounts of naphthalene (NAP) and phenanthrene (PHE) in the gaseous phase and particulate phase, respectively. The particle-size distribution exhibited the largest enrichment of total PAHs in finer particles less than 2.1 μm. Similarly, the distributions of individual species were dominated by finer particles. Most freshly emitted PAHs were liable to exist in particulate phase relative to gaseous phase. Based on the benzo[a]pyrene equivalent carcinogenic power, PAHs in particulate phase may have much stronger toxicity compared with those present in gaseous phase. The gas-particle partitioning behaviors of freshly emitted PAHs from pyrolytic processing of E-wastes were mainly regulated by absorption rather than adsorption, and the gas-particle partitioning did not reach equilibrium.
选取两种典型的电子废弃物(E-waste),研究了热解过程中多环芳烃(PAHs)的排放特征,包括排放因子、成分谱、粒径分布和气相-颗粒相分配。印刷线路板和塑料外壳的总多环芳烃的平均排放因子(EFs)分别为 2.77±1.41μg/g 和 23.65±14.52μg/g,低于煤燃烧和生物质燃烧。低分子量物质在废气中占主导地位,气态相中萘(NAP)和菲(PHE)占绝对优势,而颗粒相中则分别占绝对优势。粒径分布显示总多环芳烃在小于 2.1μm 的细颗粒中富集最多。同样,各物种的分布也以细颗粒为主。与气相相比,大部分新排放的多环芳烃更易存在于颗粒相中。基于苯并[a]芘等效致癌毒性,颗粒相中的多环芳烃可能比气相中的多环芳烃具有更强的毒性。电子废物热解过程中新鲜排放的多环芳烃的气-粒分配行为主要受吸收而不是吸附的控制,且气-粒分配未达到平衡。