Mild reductive catalytic depolymerization of lignin in a continuous flow reactor using a Cu-enhanced Pd catalyst

• PdCu offers same activity and selectivity to Pd despite 49 % lower Pd content. • 2 distinct PdCu alloys formed during reaction, smaller unordered and larger FCC. • Deactivation due to γ-Al 2 O 3 hydration, not leaching, poisoning or sintering. • Partial replacement of Pd with Cu does not affect catalyst deactivation. Mild reductive catalytic depolymerization (MRCD) of lignin offers a sustainable route to produce functionalized aromatic compounds. However, the economic viability is hindered by the need for expensive palladium (Pd) catalysts and the limited exploration of continuous flow reactors (CFRs), which are essential to achieve an adequate production scale. This study examines the impact of partial replacement of Pd with copper (Cu) on the performance, selectivity, active site characteristics, and deactivation of a γ-Al 2 O 3 supported Pd catalyst in MRCD of lignin using a CFR. Despite containing 49 % less Pd, the PdCu catalyst achieves the same depolymerization degree as the Pd catalyst over 200 min of time on stream. During the reaction, metallic Pd is formed within the Pd catalyst and both a smaller (unordered) and larger (ordered FCC) metallic PdCu phase within the PdCu catalyst. The enhanced performance of the PdCu catalyst is attributed to synergistic effects between Pd and Cu and presence of differently sized metallic phases. A minimal impact of Cu on the selectivity, even in monomer yields, was observed. For both catalysts, the primary cause of deactivation is the hydration of the γ-Al 2 O 3 support to boehmite, leading to loss of its acidity and morphological changes. Metal leaching and poisoning are insignificant, while nanoparticle growth likely arises from the reduction of the metallic phases during reaction. Only a very small amount of coke deposition is observed. Overall, the cost-effective partial replacement of Pd with of Cu forms metallic PdCu alloys during the reaction, enhancing activity without adversely affecting selectivity or deactivation.

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Publication Details

Journal
Chemical Engineering Journal Advances
Published
2025-01-27
DOI
https://doi.org/10.1016/j.ceja.2025.100710
Citations
3
Primary Topic
Lignin and Wood Chemistry
Type
article
Field-Weighted Citation Impact
2.02

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article

Mild reductive catalytic depolymerization of lignin in a continuous flow reactor using a Cu-enhanced Pd catalyst

Pieter Vermeir, Kevin M. Van Geem, Christian Hulteberg, An Verberckmoes et al.
3 citations
Chemical Engineering Journal Advances
Lignin and Wood Chemistry
2.02
article

Mild reductive catalytic depolymerization of lignin in a continuous flow reactor using a Cu-enhanced Pd catalyst

Pieter Vermeir, Kevin M. Van Geem, Christian Hulteberg, An Verberckmoes, Jeriffa De Clercq, Tibo De Saegher, Jonas Elmroth Nordlander, Jeroen Lauwaert, Boyana Atanasova, Filip Hallböök
article en
3 citations

Abstract

• PdCu offers same activity and selectivity to Pd despite 49 % lower Pd content. • 2 distinct PdCu alloys formed during reaction, smaller unordered and larger FCC. • Deactivation due to γ-Al 2 O 3 hydration, not leaching, poisoning or sintering. • Partial replacement of Pd with Cu does not affect catalyst deactivation. Mild reductive catalytic depolymerization (MRCD) of lignin offers a sustainable route to produce functionalized aromatic compounds. However, the economic viability is hindered by the need for expensive palladium (Pd) catalysts and the limited exploration of continuous flow reactors (CFRs), which are essential to achieve an adequate production scale. This study examines the impact of partial replacement of Pd with copper (Cu) on the performance, selectivity, active site characteristics, and deactivation of a γ-Al 2 O 3 supported Pd catalyst in MRCD of lignin using a CFR. Despite containing 49 % less Pd, the PdCu catalyst achieves the same depolymerization degree as the Pd catalyst over 200 min of time on stream. During the reaction, metallic Pd is formed within the Pd catalyst and both a smaller (unordered) and larger (ordered FCC) metallic PdCu phase within the PdCu catalyst. The enhanced performance of the PdCu catalyst is attributed to synergistic effects between Pd and Cu and presence of differently sized metallic phases. A minimal impact of Cu on the selectivity, even in monomer yields, was observed. For both catalysts, the primary cause of deactivation is the hydration of the γ-Al 2 O 3 support to boehmite, leading to loss of its acidity and morphological changes. Metal leaching and poisoning are insignificant, while nanoparticle growth likely arises from the reduction of the metallic phases during reaction. Only a very small amount of coke deposition is observed. Overall, the cost-effective partial replacement of Pd with of Cu forms metallic PdCu alloys during the reaction, enhancing activity without adversely affecting selectivity or deactivation.

Chemical Engineering Journal AdvancesVol. 22
HOGENT University of Applied Sciences and Arts (BE), Lund University (SE), Ghent University (BE)
Fonds Wetenschappelijk Onderzoek, Universiteit Gent, Vlaamse regering
Clean water and sanitation
Openalex Percentile: Top 16%
Lignin and Wood Chemistry
2.02
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