用于甘油催化转化的沸石基材料的挑战、前景和全面发展:综述

IF 5.2 2区 化学 Q1 CHEMISTRY, APPLIED Catalysis Today Pub Date : 2024-08-20 DOI:10.1016/j.cattod.2024.114998
Felipe Fernandes Barbosa , Adonay R. Loiola , Sibele B.C. Pergher , Tiago Pinheiro Braga
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引用次数: 0

摘要

现代社会对能源的需求促使人们向依靠可持续替代能源的方向转型。在以减少化石燃料使用为重点的现有可能性中,生物柴油产业脱颖而出。然而,作为副产品产生的过量甘油仍引发了如何更好地利用甘油的争论。一种行之有效的方法是利用平台分子(即甘油)在异相催化剂作用下获得附加值产品。沸石以其在石油工业等众多应用领域的多功能性而闻名。此外,在将甘油催化转化为丙烯醛、乙醇、丙烯酸、烯丙醇、缩酮等过程中,不同类型的铝硅酸盐也在被研究。本综述介绍了沸石的一般特性、基本原理、协同方面、理论建模、阻力和焦炭形成,以及对这些反应构成障碍的沸石局限性。这凸显了开发具有特定酸性位点的沸石材料的重要性,这些酸性位点的数量和强度应与孔隙的互联性保持同步,这样才能最大限度地提高试剂在沸石通道内的扩散,从而减少焦炭沉积对活性位点和孔隙的阻碍。据报道,一些改性方法,包括分层、同构取代、酸度调整和附加相(SMSI 效应),可作为提高甘油转化性能和抗失活性能的替代方法。涉及反应机理、焦炭沉积和应用于甘油转化的催化剂等方面的一些研究进展一直是以工艺优化为中心的研究课题,而工艺优化则转化为开发抗失活能力更强的固体。在催化性能最佳的沸石中,以下几种最为突出:BEA、MCM-22、MFI、ITQ-2、SAPO-34 和 ZSM-5。一些复杂的技术问题仍有待更好地理解,以便使甘油催化转化的可扩展性在经济上变得可行,从而引起公共和私营部门的兴趣。
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Challenges, prospects and comprehensive evolution of zeolite-based materials for the catalytic conversion of glycerol: A review

The energetic demands of modern society urge a transition that relies on alternative and sustainable sources. Among the available possibilities focused on mitigating the use of fossil fuels, the biodiesel industry stands out. However, the excess of glycerol generated as a coproduct still raises debate regarding how it could be better used. A well-established approach is the use of the platform molecule, i.e., glycerol, in the presence of heterogeneous catalysts to obtain added value products. Zeolites are well-known for their versatility in numerous applications, such as in the oil industry. Besides, different types of aluminosilicates are being studied in the catalytic conversion of glycerol to acrolein, acetol, acrylic acid, allyl alcohol, solketal, etc. This review addresses the general properties, fundaments, synergetic aspects, theoretical modeling, resistance, and coke formation, as well as the zeolites limitations that pose obstacles for those reactions. This highlights the importance of developing zeolite materials with specific acid sites, synchronizing their amount and strength with the pore interconnectivity so that reagents diffusion within the zeolitic channels can be maximized, leading to a decrease in the obstruction of active sites and pores caused by coke deposition. A number of modifications, including hierarchization, isomorphic substitution, acidity tuning, and additional phases (SMSI effect), have been reported as alternatives for improving the performance of glycerol conversion and the resistance to deactivation. Several developments involving reactional mechanisms, coke deposition, and catalysts applied to glycerol conversion have been the subject of studies centered on process optimization, which is translated into the development of solids more resistant to deactivation. Among the zeolites with the best catalytic performance, the following stand out: BEA, MCM-22, MFI, ITQ-2, SAPO-34, and ZSM-5. Some complex technical aspects still need to be better understood so that the scalability of the catalytic conversion of glycerol becomes economically feasible, thereby arousing the interest of both the public and private sectors.

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来源期刊
Catalysis Today
Catalysis Today 化学-工程:化工
CiteScore
11.50
自引率
3.80%
发文量
573
审稿时长
2.9 months
期刊介绍: Catalysis Today focuses on the rapid publication of original invited papers devoted to currently important topics in catalysis and related subjects. The journal only publishes special issues (Proposing a Catalysis Today Special Issue), each of which is supervised by Guest Editors who recruit individual papers and oversee the peer review process. Catalysis Today offers researchers in the field of catalysis in-depth overviews of topical issues. Both fundamental and applied aspects of catalysis are covered. Subjects such as catalysis of immobilized organometallic and biocatalytic systems are welcome. Subjects related to catalysis such as experimental techniques, adsorption, process technology, synthesis, in situ characterization, computational, theoretical modeling, imaging and others are included if there is a clear relationship to catalysis.
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