Catalytic hydrodeoxygenation of phenolic compounds over Ru-MoFeP/Al2O3 catalyst

Ma, Haile; Zhang, Wei; Chen, De

doi:10.1016/j.cattod.2022.10.001

Cited by 14 publications

(1 citation statement)

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“…With the swi progress of industrialization, a diverse array of carbon-based and non-organic materials, serving as agents, networks, and reagents, nd extensive application within crucial industrial sectors such as petrochemicals, cloth dyeing and coloring, polymer manufacturing, biopharmaceuticals, and process engineering. [1][2][3] The previously discussed manufacturing processes oen generate polluted water alongside intricate components. Nevertheless, contaminated water with sophisticated constituents frequently comprises a multitude of organic contaminants that prove challenging for disintegrate and are extremely poisonous.…”

Section: Introductionmentioning

confidence: 99%

Adsorption behavior of different cresols on bismuthene: a DFT study

Iqrar,

Masood,

Alarfaji

et al. 2024

RSC Adv.

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Section: Introductionmentioning

confidence: 99%

Adsorption behavior of different cresols on bismuthene: a DFT study

Iqrar,

Masood,

Alarfaji

et al. 2024

RSC Adv.

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Catalytic Hydrodeoxygenation of Phenols and Cresols to Gasoline Range Biofuels

Mohammed,

Tannous

2024

The Chemical Record

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Unlike fossil fuels, biomass has oxygen amounts exceeding 10 wt%. Hydrodeoxygenation (HDO) is a crucial step in upgrading biomass to higher heating value liquid fuels. Oxygen removal has many challenges due to the complex chemistry and the high reactivity leading to irreversible catalyst deactivation. In this study, the focus is on the catalytic HDO of aromatic oxygen‐containing model compounds in biomass: phenols and cresols. In the current work, literature on catalytic HDO of phenols using molecular hydrogen is reviewed, with a focus on non‐nickel‐based mono‐ and bi‐metallic catalysts, as nickel‐based catalysts were reviewed elsewhere. In addition, the catalytic HDO of m‐cresol using molecular hydrogen is examined. This review also addresses the use of hydrogen donors for the HDO of phenols and cresols. The operating conditions, catalysts, products, and yields are summarized to find the catalyst with promising activity and high selectivity toward aromatics. A critical review of the reactions that successfully led to HDO is presented and research gaps related to the HDO of phenols and cresols are highlighted. The conclusions provide potential successful catalyst combinations that can be used for HDO of phenols, cresols, and liquid aromatic hydrocarbons.

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