Benedetti Vittoria, Ail Snehesh Shivananda, Patuzzi Francesco, Baratieri Marco
Faculty of Science and Technology, Free University of Bolzano, Bolzano, Italy.
Front Chem. 2019 Mar 13;7:119. doi: 10.3389/fchem.2019.00119. eCollection 2019.
This study responds to the need of finding innovative routes for valorizing char derived from biomass gasification. Char is currently treated as a waste representing an energetic and economic loss for plant owners. However, it displays many similarities to activated carbon (AC) and could replace it in several applications. In this regard, the current work investigates the use of gasification derived char as catalyst support in dry reforming of methane (DRM) reactions. Char collected from a commercial biomass gasifier currently in operation was characterized and employed for the synthesis of cobalt catalysts. The catalysts were characterized and tested in an atmospheric pressure fixed bed reactor operating at 850°C with CH:CO = 1 and a weight hourly space velocity of 6,500 mL g h. The effectiveness of the synthesized catalysts was defined based on CO and CH conversions, the corresponding H and CO yields and their stability. Accordingly, catalysts were synthesized with cobalt loading of 10, 15 and 20 wt.% on untreated and HNO treated char, and the catalyst with optimum comparative performance was promoted with 2 wt.%MgO. Catalysts prepared using untreated char showed low average conversions of 23 and 17% for CO and CH, yields of 1 and 14% for H and CO, and deactivated after few minutes of operation. Higher metal loadings corresponded to lower conversion and yields. Although HNO treatment slightly increased conversions and yields and enhanced the stability of the catalyst, the catalyst deactivated again after few minutes. On the contrary, MgO addition boosted the catalyst performances leading to conversions (95 and 94% for CO and CH) and yields (44 and 53% for H and CO) similar to what obtained using conventional supports such as AlO. Moreover, MgO catalysts proved to be very stable during the whole duration of the test.
本研究旨在满足寻找生物质气化衍生炭增值创新途径的需求。目前,炭被视为一种废物,对工厂所有者来说意味着能源和经济损失。然而,它与活性炭(AC)有许多相似之处,并且在一些应用中可以替代活性炭。在这方面,当前的工作研究了气化衍生炭作为甲烷干重整(DRM)反应中催化剂载体的用途。对从目前正在运行的商业生物质气化炉收集的炭进行了表征,并将其用于合成钴催化剂。在常压固定床反应器中对催化剂进行表征和测试,该反应器在850°C下运行,CH:CO = 1,重量时空速为6500 mL g h。基于CO和CH的转化率、相应的H和CO产率及其稳定性来定义合成催化剂的有效性。因此,在未处理和经HNO处理的炭上合成了钴负载量为10、15和20 wt.%的催化剂,并且用2 wt.%的MgO促进具有最佳比较性能的催化剂。使用未处理炭制备的催化剂显示出较低的平均转化率,CO和CH分别为23%和17%,H和CO的产率分别为1%和14%,并且在运行几分钟后失活。较高的金属负载量对应较低的转化率和产率。尽管HNO处理略微提高了转化率和产率并增强了催化剂的稳定性,但催化剂在几分钟后再次失活。相反,添加MgO提高了催化剂性能,导致转化率(CO和CH分别为95%和94%)和产率(H和CO分别为44%和53%)与使用传统载体(如AlO)时获得的结果相似。此外,MgO催化剂在整个测试期间都非常稳定。