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Cadmium isotope fractionation during coal combustion: Insights from two US coal-fired power plants

机译:煤燃烧过程中的镉同位素分馏:来自两个美国燃煤电厂的见解

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Coal combustion, one of the principal energy sources of electricity in the United States, produces over 100 million tons of coal combustion products (CCPs) per year in the U.S. The reuse and disposal of CCPs has the potential to release toxic trace elements, including cadmium (Cd), into the environment. In this study, we investigated CCPs, including bottom ash (BA), economizer fly ash (EFA), and fly ash (FA), as well as feed coal (FC) and pulverized coal (PC) collected from two U.S. coal-fired power plants in New Mexico and Ohio with different coal supplies. The New Mexico plant uses high volatile C bituminous, low-sulfur coals mined from the San Juan Basin (Cretaceous Fruitland Formation) and the Ohio plant uses high volatile A bituminous, high-sulfur central Appalachian Basin coals (Upper Pennsylvanian Monongahela Formation). Mineralogical and elemental analysis showed that these CCP samples consist of similar to 70% amorphous Al-Si-rich glasses and similar to 30% mineral phases of quartz (SiO2) and mullite (Ai(6)Si(2)O(13)). The Cd isotope compositions (delta Cd-14, normalized to NIST Cd standard 3108) of FA and EFA samples (ranging from -0.51 to + 0.47%o) are distinctively heavier than those of BA samples ( - 0.75 to - 0.52%o) in both power plants. We interpret this Cd isotope difference as a result of Cd condensation from the gas phase during flue gas cooling, instead of evaporation of Cd phase during coal combustion. Cd condensation is the main process to generate the isotopically heavy Cd signatures that preferentially partition on the fine FA particles. We also investigated Cd isotope compositions in different leachate products from a series of batch-leaching experiments with these CCPs, using diluted acetic acid, hydroxyl ammonium chloride, hydrogen peroxide followed by ammonium acetate, and 5% nitric acid, as a possible means to identify CCP-released Cd in the environment. Unusually and significantly heavier Cd isotope compositions were observed in each le
机译:煤炭燃烧是美国的主要能源来源之一,美国每年生产超过1亿吨煤炭燃烧产品(CCP),CCP的再利用和处置具有潜力释放有毒的微量元素,包括镉(CD),进入环境。在这项研究中,我们调查了CCP,包括底灰(BA),节能粉煤灰(EFA)和飞灰(FA),以及从两个美国燃煤收集的饲料煤(FC)和粉煤(PC)新墨西哥州和俄亥俄州的发电厂与不同的煤炭供应。新墨西哥州植物采用高挥发性C沥青,低硫煤,从圣胡安盆地(白垩纪果实形成)和俄亥俄州植物使用高挥发性,高硫磺中央阿巴拉契亚盆地煤(上宾夕法尼亚州Monongahela形成)。矿物学和元素分析表明,这些CCP样品与富含70%的无定形Al-Si的玻璃等组成,类似于石英(SiO 2)和莫来石的30%矿物相(Ai(6)Si(2)O(13)) 。 FA和EFA样品的CD同位素组合物(达到NIST CD标准3108标准化为NIST CD标准3108)比BA样品( - 0.75至-0.52%O)显着更重在两个发电厂。我们将该CD同位素差异解释为从烟气冷却过程中的气相中的Cd凝结,而不是在煤燃烧期间蒸发CD相。 CD凝结是产生优先分配在精细FA颗粒上的同位素重的CD签名的主要过程。我们还研究了不同渗滤液产品中的CD同位素组合物,其与这些CCPS的一系列批次浸出实验,使用稀醋酸,氯化铵,过氧化氢,过氧化氢,5%硝酸,作为识别的可能手段CCP发布的环境中的CD。在每个LE中观察到异常而显着较重的CD同位素组合物

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