Xiao Ye, Montes Vicente, Hill Josephine M
Department of Chemical and Petroleum Engineering, Schulich School of Engineering, University of Calgary, 2500 University Drive NW, Calgary, Alberta, T2N 1N4, Canada; School of Environmental Science and Engineering, Sun Yat-Sen University, Guangzhou, 510006, China.
Department of Chemical and Petroleum Engineering, Schulich School of Engineering, University of Calgary, 2500 University Drive NW, Calgary, Alberta, T2N 1N4, Canada; Department of Chemical Engineering and Physis Chemistry, University Institute of Research in Water, Climate Change and Sustainability (IACYS), University of Extremadura, Badajoz, Spain.
Chemosphere. 2022 Dec;308(Pt 2):136340. doi: 10.1016/j.chemosphere.2022.136340. Epub 2022 Sep 7.
Petroleum coke (petcoke) containing sulphur has limited direct applications, but stockpiling the material creates an environmental issue. Although chemical activation can be used to valorise the petcoke to activated carbon, sulphur is released creating alternative environmental problems. In this study, a new activation method for high sulphur content (∼6.5 wt%) petcoke was developed to retain sulphur and prepare transition metal sulphide catalysts simultaneously. Petcoke was mixed with tungsten and nickel precursors and then activated by KOH at 600 °C in the presence of steam. After washing, the activated petcoke had a sulphur content of 5.1 wt%, which was much higher than that in the absence of steam during activation (0.4 wt%). Sulphur was also retained (>4 wt% of sulphur) when other transition metals including molybdenum and cobalt were used. Characterization by XRD, XPS, and SEM-EDS suggested that sulphur was retained on the activated petcoke in the form of metal sulphides. Further thermodynamic analysis of the system revealed that in the presence of steam an HS/H mixture was generated, and this mixture promoted the formation of the metal sulphide species when metal precursors were introduced. The prepared metal sulphide catalysts were active for several reactions including the photoreduction of CO. Overall, this study provided an effective method to prepare metal sulphide catalysts from sulphur containing carbonaceous waste.
含硫石油焦(石油焦)的直接应用有限,但储存该材料会引发环境问题。尽管化学活化可用于将石油焦转化为活性炭,但会释放硫,从而产生其他环境问题。在本研究中,开发了一种针对高硫含量(约6.5 wt%)石油焦的新活化方法,以保留硫并同时制备过渡金属硫化物催化剂。将石油焦与钨和镍前驱体混合,然后在蒸汽存在下于600℃用KOH活化。洗涤后,活化后的石油焦硫含量为5.1 wt%,远高于活化过程中无蒸汽时的硫含量(0.4 wt%)。当使用包括钼和钴在内的其他过渡金属时,硫也能被保留(硫含量>4 wt%)。XRD、XPS和SEM-EDS表征表明,硫以金属硫化物的形式保留在活化后的石油焦上。对该体系的进一步热力学分析表明,在蒸汽存在下会生成HS/H混合物,当引入金属前驱体时,该混合物促进了金属硫化物物种的形成。所制备的金属硫化物催化剂对包括CO光还原在内的多种反应具有活性。总体而言,本研究提供了一种从含硫碳质废料制备金属硫化物催化剂的有效方法。