Geology Department, Faculty of Science, Taibah University, Al-Madinah Al-Munawwarah, KSA.
Environ Sci Technol. 2011 Nov 15;45(22):9799-805. doi: 10.1021/es200695e. Epub 2011 Oct 19.
With the increase in the awareness of the public in the environmental impact of oil shale utilization, it is of interest to reveal the mobility of potentially toxic trace elements in spent oil shale. Therefore, the Cr and As oxidation state in a representative Jordanian oil shale sample from the El-Lajjoun area were investigated upon different lab-scale furnace treatments. The anaerobic pyrolysis was performed in a retort flushed by nitrogen gas at temperatures in between 600 and 800 °C (pyrolytic oil shale, POS). The aerobic combustion was simply performed in porcelain cups heated in a muffle furnace for 4 h at temperatures in between 700 and 1000 °C (burned oil shale, BOS). The high loss-on-ignition in the BOS samples of up to 370 g kg(-1) results from both calcium carbonate and organic carbon degradation. The LOI leads to enrichment in the Cr concentrations from 480 mg kg(-1) in the original oil shale up to 675 mg kg(-1) in the ≥ 850 °C BOS samples. Arsenic concentrations were not much elevated beyond that in the average shale standard (13 mg kg(-1)). Synchrotron-based X-ray absorption near-edge structure (XANES) analysis revealed that within the original oil shale the oxidation states of Cr and As were lower than after its aerobic combustion. Cr(VI) increased from 0% in the untreated or pyrolyzed oil shale up to 60% in the BOS ash combusted at 850 °C, while As(V) increased from 64% in the original oil shale up to 100% in the BOS ash at 700 °C. No Cr was released from original oil shale and POS products by the European compliance leaching test CEN/TC 292 EN 12457-1 (1:2 solid/water ratio, 24 h shaking), whereas leachates from BOS samples showed Cr release in the order of one mmol L(-1). The leachable Cr content is dominated by chromate as revealed by catalytic adsorptive stripping voltammetry (CAdSV) which could cause harmful contamination of surface and groundwater in the semiarid environment of Jordan.
随着公众对油页岩利用的环境影响意识的提高,揭示潜在有毒痕量元素在废弃油页岩中的迁移性变得很有意义。因此,研究了来自约旦 El-Lajjoun 地区的代表性油页岩样品在不同实验室规模的炉处理下的 Cr 和 As 氧化态。在氮气吹扫的容器中进行无氧热解,温度在 600 至 800°C 之间(热解油页岩,POS)。有氧燃烧则简单地在马弗炉中加热瓷杯进行,温度在 700 至 1000°C 之间(燃烧油页岩,BOS),持续 4 小时。BOS 样品高达 370 g kg(-1) 的高失重量(LOI)是由碳酸钙和有机碳降解引起的。LOI 导致 Cr 浓度从原始油页岩中的 480 mg kg(-1)增加到≥850°C BOS 样品中的 675 mg kg(-1)。砷浓度并没有比平均页岩标准(13 mg kg(-1))高多少。基于同步加速器的 X 射线吸收近边结构(XANES)分析表明,在原始油页岩中,Cr 和 As 的氧化态低于其有氧燃烧后。Cr(VI)从未经处理或热解油页岩中的 0%增加到 850°C 燃烧的 BOS 灰分中的 60%,而 As(V)从原始油页岩中的 64%增加到 700°C 燃烧的 BOS 灰分中的 100%。欧洲合规浸出试验 CEN/TC 292 EN 12457-1(1:2 固/水比,24 小时摇晃)未从原始油页岩和 POS 产品中释放出 Cr,而 BOS 样品的浸出液中 Cr 的释放量为一个 mmol L(-1)。通过催化吸附剥离伏安法(CAdSV)表明,可溶 Cr 含量主要由铬酸盐组成,这可能会对约旦半干旱环境中的地表水和地下水造成有害污染。