CO₂-to-carbonates via reaction–separation coupling: pilot performance of continuous DMC/DPC

This study develops and demonstrates integrated pilot plants for the continuous production of dimethyl carbonate (DMC) and diphenyl carbonate (DPC) as part of a carbon capture and utilization (CCU) strategy. DMC was synthesized from urea (derived from CO₂ + NH₃) and methanol over a zirconium-based catalyst. Across three campaigns totaling 211 h, the unit produced 570.5 kg of DMC, corresponding to an overall yield of 85.9% relative to the 663.9 kg theoretical maximum from 442.3 kg of urea. The product reached 99.93% purity, and electrolyte testing showed no statistically significant differences versus commercial battery-grade DMC. DPC was obtained via transesterification of phenol with DMC using a reactor–distillation configuration that enables in-situ removal of methanol. Over ~ 200 h of continuous operation, phenol conversion was ~ 100% and 65.8 kg of DPC were collected, equal to an overall yield of 32.1% versus the 204.98 kg theoretical limit. Yield shortfalls were attributed to hold-up of intermediates (e.g., phenyl methyl carbonate) and high-boiling residues within equipment. Both trains exhibited stable operability without catalyst bed plugging, and product specifications were consistently met. These results validate the technical feasibility of CCU-based carbonate ester production and identify clear levers—enhanced methanol removal, additional reaction stages, and tighter reaction–separation coupling—for yield intensification and scale-up.

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Publication Details

Journal
Advances in Industrial and Engineering Chemistry
Published
2025-12-23
DOI
https://doi.org/10.1007/s44405-025-00039-4
Primary Topic
Carbon dioxide utilization in catalysis
Type
article
Field-Weighted Citation Impact
0.00

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article

CO₂-to-carbonates via reaction–separation coupling: pilot performance of continuous DMC/DPC

Namgyu Son, Wonsang Jung, Gang Min Lee, Joonwoo Kim et al.
Advances in Industrial and Engineering Chemistry
Carbon dioxide utilization in catalysis
article

CO₂-to-carbonates via reaction–separation coupling: pilot performance of continuous DMC/DPC

Namgyu Son, Wonsang Jung, Gang Min Lee, Joonwoo Kim, Jong Cheol Yun, Sang Ho Lee, Sukyong Jung
article en

Abstract

This study develops and demonstrates integrated pilot plants for the continuous production of dimethyl carbonate (DMC) and diphenyl carbonate (DPC) as part of a carbon capture and utilization (CCU) strategy. DMC was synthesized from urea (derived from CO₂ + NH₃) and methanol over a zirconium-based catalyst. Across three campaigns totaling 211 h, the unit produced 570.5 kg of DMC, corresponding to an overall yield of 85.9% relative to the 663.9 kg theoretical maximum from 442.3 kg of urea. The product reached 99.93% purity, and electrolyte testing showed no statistically significant differences versus commercial battery-grade DMC. DPC was obtained via transesterification of phenol with DMC using a reactor–distillation configuration that enables in-situ removal of methanol. Over ~ 200 h of continuous operation, phenol conversion was ~ 100% and 65.8 kg of DPC were collected, equal to an overall yield of 32.1% versus the 204.98 kg theoretical limit. Yield shortfalls were attributed to hold-up of intermediates (e.g., phenyl methyl carbonate) and high-boiling residues within equipment. Both trains exhibited stable operability without catalyst bed plugging, and product specifications were consistently met. These results validate the technical feasibility of CCU-based carbonate ester production and identify clear levers—enhanced methanol removal, additional reaction stages, and tighter reaction–separation coupling—for yield intensification and scale-up.

Advances in Industrial and Engineering ChemistryVol. 1(1)
Mando Corporation (South Korea) (KR), Research Institute of Industrial Science and Technology (KR), Korea Institute of Industrial Technology (KR)
Ministry of Trade, Industry and Energy, Korea Institute of Energy Technology Evaluation and Planning
Openalex Percentile: Top 46%
Carbon dioxide utilization in catalysis
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