Heterogeneous catalysis is a promising technology for the valorization of renewable biomass to sustainable advanced fuels and fine chemicals. Porosity and nanostructure are the most versatile features of heterogeneous solid catalysts, which can greatly determine the accessibility of specific active sites, reaction mechanisms, and the selectivity of desirable products. Hence, the precise tuning of porosity and nanostructure has been a potential strategy towards developing novel solid catalysts with indispensable characteristics for efficient biomass valorization. Herein, we present a timely and comprehensive review of the recent advances in catalytic biomass conversions over microporous zeolites, mesoporous silicas, and nanostructured metals/metal oxides. This review covers the catalytic processing of both edible (lipids and starch) and non-edible (lignocellulose) biomass as well as their derived compounds, along with a systematic evaluation of catalyst reusability/kinetic/mechanistic aspects in the relevant processes. The key parameters essential for tailoring particle size, morphology, porosity, acid–base, and redox properties of solid catalysts are emphasized, while discussing the ensuing catalytic effects towards the selective conversion of biomass into desirable chemicals. Special attention has been drawn to understand the role of water in liquid phase biomass conversions as well as the hydrothermal stability and the deactivation of nanoporous catalysts. We believe this comprehensive review will provide new insights towards developing state-of-the-art solid catalysts with well-defined porosity and nanoscale properties for viable biomass conversion.

/pdf/advances-in-porous-and-nanoscale-catalysts-for-viable-41c9h3z96y.pdf

Advances in porous and nanoscale catalysts for viable biomass conversion.

Hierarchical zeolites combine the intrinsic catalytic properties of microporous zeolites and the enhanced access and transport of the additional meso- and/or macroporous system. These materials are the most desirable catalysts and sorbents for industry and become a highly evolving field of important current interests. In addition to the enhanced mass transfer leading to high activity, selectivity, and cycle time, another essential merit of the hierarchical structure in zeolite materials is that it can significantly improve the utilization effectiveness of zeolite materials resulting in the minimum energy, time, and raw materials consumption. Substantial progress has been made in the synthesis, characterization, and application of hierarchical zeolites. Herein, we provide an overview of recent achievements in the field, highlighting the significant progress in the past decade on the development of novel and remarkable strategies to create an additional pore system in zeolites. The most innovative synthesis approaches are reviewed according to the principle, versatility, effectiveness, and degree of reality while establishing a firm link between the preparation route and the resultant hierarchical pore quality in zeolites. Zeolites with different hierarchically porous structures, i.e., micro-mesoporous structure, micro-macroporous structure, and micro-meso-macroporous structure, are then analyzed in detail with concrete examples to illustrate their benefits and their fabrications. The significantly improved performances in catalytic, environmental, and biological applications resulting from enhanced mass transport properties are discussed through a series of representative cases. In the concluding part, we envision the emergence of "material-properties-by-quantitative and real rational design" based on the "generalized Murray's Law" that enables the predictable and controlled productions of bioinspired hierarchically structured zeolites. This Review is expected to attract important interests from catalysis, separation, environment, advanced materials, and chemical engineering fields as well as biomedicine for artificial organ and drug delivery systems.

Hierarchically Structured Zeolites: From Design to Application.

https://backend.orbit.dtu.dk/ws/files/129909915/Leaching_review_draft_final_AR.pdf

Deactivation of solid catalysts in liquid media: the case of leaching of active sites in biomass conversion reactions

Titanium silicalite-1 (TS-1) is a zeolitic material with MFI framework structure, in which 1 to 2 per cent of the silicon atoms are substituted for titanium atoms. It is widely used in industry owing to its ability to catalytically epoxidize olefins with hydrogen peroxide (H2O2), leaving only water as a byproduct1,2; around one million tonnes of propylene oxide are produced each year using this process3. The catalytic properties of TS-1 are generally attributed to the presence of isolated Ti(IV) sites within the zeolite framework1. However, despite almost 40 years of experimental and computational investigation4-10, the structure of these active Ti(IV) sites is unconfirmed, owing to the challenges of fully characterizing TS-1. Here, using a combination of spectroscopy and microscopy, we characterize in detail a series of highly active and selective TS-1 propylene epoxidation catalysts with well dispersed titanium atoms. We find that, on contact with H217O2, all samples exhibit a characteristic solid-state 17O nuclear magnetic resonance signature that is indicative of the formation of bridging peroxo species on dinuclear titanium sites. Further, density functional theory calculations indicate that cooperativity between two titanium atoms enables propylene epoxidation via a low-energy reaction pathway with a key oxygen-transfer transition state similar to that of olefin epoxidation by peracids. We therefore propose that dinuclear titanium sites, rather than isolated titanium atoms in the framework, explain the high efficiency of TS-1 in propylene epoxidation with H2O2. This revised view of the active-site structure may enable further optimization of TS-1 and the industrial epoxidation process.

/pdf/efficient-epoxidation-over-dinuclear-sites-in-titanium-4xb464ziea.pdf

Efficient epoxidation over dinuclear sites in titanium silicalite-1.

Hydrogen peroxide (H2O2) is a highly effective, green oxidant that has found application in sectors ranging from the synthesis of fine chemicals and waste stream treatment to the extraction of precious metals and the bleaching of paper pulp and textiles. The growing demand for H2O2 has seen it become one of the 100 most important chemicals in the world. The direct synthesis of H2O2 from H2 and O2 has been a challenge for the scientific community for over 100 years and represents an attractive alternative to the current means of production. Herein we discuss the historical perspective of the direct synthesis process, the recent literature regarding catalyst design and the role of additives as well as the application of H2O2 as an in situ oxidant. We discuss the key problems that remain and conclude that although there has been progress with respect to the selectivity of hydrogen utilisation, there is a need to now concentrate on catalyst activity as the key remaining problem requiring a solution is the concentration of H2O2 that can be achieved especially in flow reactors.

/pdf/recent-advances-in-the-direct-synthesis-of-h2o2-42mn8eubjf.pdf

Recent Advances in the Direct Synthesis of H2O2

Green and efficient epoxidation of propylene with hydrogen peroxide (HPPO process) catalyzed by hollow TS-1 zeolite: A 1.0 kt/a pilot-scale study

Hierarchical TS-1 with intracrystalline voids could be synthesized by post-modification with tetrapropyl ammonium hydroxide (TPAOH), however the process was supposed to be restrained by the charge balance effect. In order to release the constraint, NH3·H2O was introduced in the post-modification. The influences of the TPAOH/NH3·H2O modification, the TPAOH concentration and the modification time on the physiochemical properties were studied. The dissolution process and recrystallization process were observed in the combined modification, and both of them were intensified by the NH3·H2O introduced, indicating that the constraint on the OH− diffusion was released. Owing to the intensified processes, the TPAOH concentration and post-modification time could be reduced, and hierarchical TS-1 with relative high crystallinity, less defect sites and a larger secondary pore volume (about 0.18 cm3 g−1) was achieved in 4 h. However, the combined-modification exerted little influence on the chemical composition and acidity, and the microporous properties were almost the same with that of TS-1 modified with TPAOH only. The secondary porosity in the combined-modified samples were mainly intracrystalline voids, and grooves on the surface were also found. Although extra-framework titanium species were created by the post-modification, part of the titanium was still in the framework position. The catalytic activity was evaluated by phenol hydroxylation and 1-octene epoxidation, and better catalytic activity was achieved for the improved accessibility of the active sites.

Hierarchical TS-1 synthesized effectively by post-modification with TPAOH and ammonium hydroxide

Irreversible deactivation of hollow TS-1 zeolite caused by the formation of acidic amorphous TiO2–SiO2 nanoparticles in a commercial cyclohexanone ammoximation process

The synthesis, characterization and catalytic activity of the hierarchical TS-1 with the intracrystalline voids and grooves

Hierarchical TS-1 synthesized via the dissolution-recrystallization process: Influence of ammonium salts

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