State-of-the-art advancements in the thermocatalytic conversion of CO2 into ethanol and higher alcohols: recent progress in catalyst development and reaction mechanisms

• A systematic literature review of CO 2 hydrogenation into ethanol/HA was conducted. • The discussion covers catalyst systems derived from noble metals, Cu, Co, and Fe. • The influence of promoters, supports and alkali metal(s) doping are explored. • Comprehensive studies of reaction mechanisms are analyzed. • Strategies to enhance ethanol and HA selectivity are proposed. The production of ethanol and higher alcohols (HA) via CO 2 hydrogenation with achieving high product selectivity and catalyst stability is a difficult scientific and technological challenge due to chemical inertness of CO 2 , complexity in various reaction routes, and uncontrollability of C–C coupling from untamed surface moieties in HA synthesis. One of the main solutions is a catalyst design, which can overcome these issues. Hence, in this review, we summarize and analyze the recent advances in thermocatalytic direct CO 2 hydrogenation into ethanol and HA in batch and continuous fixed-bed reactors. The introductory section delves into the discourse surrounding carbon capture and utilization, highlighting the constraints imposed by reaction thermodynamics, and emphasizing the indispensable role of catalysts in the conversion of CO 2 to ethanol and HA. The second section highlights the potential promising catalyst families, in a batch reactor, including modified Cu-based catalysts, modified Co-based catalysts, and a noble-metal catalysts, together with various promoters, supports, and solvent effects specified in each case. The third section reviews the family most active catalysts, but in continuous fixed-bed reactor, including modified Cu-, Co–, Fe-based and noble metals catalysts. The fourth section reviews the possible reaction mechanisms (CO-mediated pathway, formate/methoxy-mediated pathway, and C–C coupling pathways) for ethanol and HA production. Ultimately, the conclusion and future perspectives are provided to offer a forward-looking assessment of catalyst development including approaches to enhance selectivity towards ethanol/HA based on the available experimental results.

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Publication Details

Journal
Chemical Engineering Journal
Published
2024-12-12
DOI
https://doi.org/10.1016/j.cej.2024.158467
Citations
21
Primary Topic
Catalysts for Methane Reforming
Type
article
Field-Weighted Citation Impact
2.24

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article

State-of-the-art advancements in the thermocatalytic conversion of CO2 into ethanol and higher alcohols: recent progress in catalyst development and reaction mechanisms

Andrii Kostyniuk, Blaž Likozar
21 citations
Chemical Engineering Journal
Catalysts for Methane Reforming
2.24
article

State-of-the-art advancements in the thermocatalytic conversion of CO2 into ethanol and higher alcohols: recent progress in catalyst development and reaction mechanisms

Andrii Kostyniuk, Blaž Likozar
article en
21 citations

Abstract

• A systematic literature review of CO 2 hydrogenation into ethanol/HA was conducted. • The discussion covers catalyst systems derived from noble metals, Cu, Co, and Fe. • The influence of promoters, supports and alkali metal(s) doping are explored. • Comprehensive studies of reaction mechanisms are analyzed. • Strategies to enhance ethanol and HA selectivity are proposed. The production of ethanol and higher alcohols (HA) via CO 2 hydrogenation with achieving high product selectivity and catalyst stability is a difficult scientific and technological challenge due to chemical inertness of CO 2 , complexity in various reaction routes, and uncontrollability of C–C coupling from untamed surface moieties in HA synthesis. One of the main solutions is a catalyst design, which can overcome these issues. Hence, in this review, we summarize and analyze the recent advances in thermocatalytic direct CO 2 hydrogenation into ethanol and HA in batch and continuous fixed-bed reactors. The introductory section delves into the discourse surrounding carbon capture and utilization, highlighting the constraints imposed by reaction thermodynamics, and emphasizing the indispensable role of catalysts in the conversion of CO 2 to ethanol and HA. The second section highlights the potential promising catalyst families, in a batch reactor, including modified Cu-based catalysts, modified Co-based catalysts, and a noble-metal catalysts, together with various promoters, supports, and solvent effects specified in each case. The third section reviews the family most active catalysts, but in continuous fixed-bed reactor, including modified Cu-, Co–, Fe-based and noble metals catalysts. The fourth section reviews the possible reaction mechanisms (CO-mediated pathway, formate/methoxy-mediated pathway, and C–C coupling pathways) for ethanol and HA production. Ultimately, the conclusion and future perspectives are provided to offer a forward-looking assessment of catalyst development including approaches to enhance selectivity towards ethanol/HA based on the available experimental results.

Chemical Engineering JournalVol. 503
National Institute of Chemistry (SI)
Javna Agencija za Raziskovalno Dejavnost RS
Openalex Percentile: Top 11%
Catalysts for Methane Reforming
2.24
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