Petala Athanasia, Noe Antigoni, Frontistis Zacharias, Drivas Charalampos, Kennou Stella, Mantzavinos Dionissios, Kondarides Dimitris I
Department of Chemical Engineering, University of Patras, Caratheodory 1, GR-26504 Patras, Greece.
Department of Chemical Engineering, University of Patras, Caratheodory 1, GR-26504 Patras, Greece.
J Hazard Mater. 2019 Jun 15;372:52-60. doi: 10.1016/j.jhazmat.2018.03.008. Epub 2018 Mar 13.
Cobalt-promoted bismuth vanadate photocatalysts of variable cobalt content (0-1.0 wt.%) were synthesized and characterized with various techniques including BET, XRD, DRS, XPS and TEM. BiVO exists in the monoclinic scheelite structure, while cobalt addition improves the absorbance in the visible region although it does not affect the band gap energy of BiVO. Cobalt exists in the form of well-dispersed CoO nanocrystallites, which are in intimate contact with the much larger BiVO nanoparticles. Photocatalytic activity was evaluated for the degradation of propyl paraben (PP) under simulated solar radiation. The activity of pristine BiVO is significantly improved adding small amounts of cobalt and is maximized for the catalyst containing 0.5 wt.% Co. PP degradation in ultrapure pure water increases with increasing photocatalyst loading (100 mg/L to 1.5 g/L), and decreasing PP concentration (1600-200 μg/L). Experiments in bottled water, as well as in pure water spiked with bicarbonate and chloride ions showed little effect of non-target inorganics on degradation. Conversely, degradation is severely impeded in secondary treated wastewater. The enhancement of the photocatalytic activity of the synthesized catalysts is attributed to efficient electron-hole separation, achieved at the p-n junction formed between the p-type CoO and the n-type BiVO semiconductors.
合成了钴含量可变(0 - 1.0 wt.%)的钴促进钒酸铋光催化剂,并用包括BET、XRD、DRS、XPS和TEM在内的各种技术对其进行了表征。BiVO以单斜白钨矿结构存在,虽然添加钴不影响BiVO的带隙能量,但能提高其在可见光区域的吸光度。钴以分散良好的CoO纳米微晶形式存在,这些纳米微晶与大得多的BiVO纳米颗粒紧密接触。在模拟太阳辐射下评估了光催化剂对尼泊金丙酯(PP)降解的光催化活性。添加少量钴可显著提高原始BiVO的活性,含0.5 wt.% Co的催化剂活性最高。在超纯水中,PP的降解随光催化剂负载量增加(100 mg/L至1.5 g/L)和PP浓度降低(1600 - 200 μg/L)而增加。在瓶装水中以及在添加了碳酸氢根和氯离子的纯水中进行的实验表明,非目标无机物对降解几乎没有影响。相反,在二级处理后的废水中,降解受到严重阻碍。合成催化剂光催化活性的增强归因于在p型CoO和n型BiVO半导体之间形成的p - n结处实现了有效的电子 - 空穴分离。