Lignin waste-based low-cost porous carbon for efficient and stable CO2 capture

• Synthesis of low-cost porous carbon CO 2 adsorbents from lignin waste via one-step carbonization/activation method. • Utilization of K 2 CO 3 activator and high calcination temperature enabled the formation of numerous micropores below 2 nm and mesopores in the range of 2–4 nm. • Optimal porous carbon demonstrates exceptional CO 2 capture capacity up to 3.75 mmol/g at 1 bar and 25 °C. • Excellent CO 2 /N 2 selectivity of 57.2, low regeneration energy Q st of 15.9–23.8 kJ/mol and excellent stability over multiple adsorption/desorption cycles highlight application potentials. Developing a low-cost and renewable porous carbon-based CO 2 adsorbent with excellent CO 2 capture capacity, selectivity, stability and low regeneration energy is a contemporary research subject worldwide, especially in the context of a circular and carbon neutral economy. Herein, we report the synthesis of novel low-cost porous carbon materials for highly efficient CO 2 capture prepared from abundant lignin waste via a one-step direct activation/carbonization method. Upon optimization of the activation temperature and activator concentration, the optimal carbon adsorbent material L-K-2–750 with K 2 CO 3 as activator, K 2 CO 3 /lignin mass ratio of 2/3 and activation temperature of 750 °C, exhibited a high specific surface area (797 m 2 /g) and high total pore volume (0.33 cm 3 /g). It demonstrated an excellent CO 2 adsorption capacity of 3.75 mmol/g at 25 °C and 1 bar, which is comparable to or better than the CO₂ adsorption capacities reported in the literature (1.1–4.4 mmol/g). Adsorption/desorption cycling experiments revealed excellent stability over five cycles with <2 % loss of adsorption capacity. CO 2 /N 2 selectivity experiments showed an excellent selectivity of 57.2 in a CO 2 /N 2 mixture (15:85). The Isosteric Adsorption Heat (Q st ) level of 15.9–23.8 kJ/mol confirmed low regeneration energy, thus making this material highly promising for practical applications.

Authors

Institutions

Publication Details

Journal
Results in Engineering
Published
2025-06-27
DOI
https://doi.org/10.1016/j.rineng.2025.105962
Citations
4
Primary Topic
Carbon Dioxide Capture Technologies
Type
article
Field-Weighted Citation Impact
2.85
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Lignin waste-based low-cost porous carbon for efficient and stable CO2 capture

Yuhe Liao, Fu‐An Guo, Shao‐Tao Bai, Ruiqin Zhang et al.
4 citations
Results in Engineering
Carbon Dioxide Capture Technologies
2.85
article

Lignin waste-based low-cost porous carbon for efficient and stable CO2 capture

Yuhe Liao, Fu‐An Guo, Shao‐Tao Bai, Ruiqin Zhang, Haiming Yang, Boshi Li, Zhongyao Liang, Chenguang Bai, Changle Wang, Jiong Sun, Salman Qadira
article en
4 citations

Abstract

• Synthesis of low-cost porous carbon CO 2 adsorbents from lignin waste via one-step carbonization/activation method. • Utilization of K 2 CO 3 activator and high calcination temperature enabled the formation of numerous micropores below 2 nm and mesopores in the range of 2–4 nm. • Optimal porous carbon demonstrates exceptional CO 2 capture capacity up to 3.75 mmol/g at 1 bar and 25 °C. • Excellent CO 2 /N 2 selectivity of 57.2, low regeneration energy Q st of 15.9–23.8 kJ/mol and excellent stability over multiple adsorption/desorption cycles highlight application potentials. Developing a low-cost and renewable porous carbon-based CO 2 adsorbent with excellent CO 2 capture capacity, selectivity, stability and low regeneration energy is a contemporary research subject worldwide, especially in the context of a circular and carbon neutral economy. Herein, we report the synthesis of novel low-cost porous carbon materials for highly efficient CO 2 capture prepared from abundant lignin waste via a one-step direct activation/carbonization method. Upon optimization of the activation temperature and activator concentration, the optimal carbon adsorbent material L-K-2–750 with K 2 CO 3 as activator, K 2 CO 3 /lignin mass ratio of 2/3 and activation temperature of 750 °C, exhibited a high specific surface area (797 m 2 /g) and high total pore volume (0.33 cm 3 /g). It demonstrated an excellent CO 2 adsorption capacity of 3.75 mmol/g at 25 °C and 1 bar, which is comparable to or better than the CO₂ adsorption capacities reported in the literature (1.1–4.4 mmol/g). Adsorption/desorption cycling experiments revealed excellent stability over five cycles with <2 % loss of adsorption capacity. CO 2 /N 2 selectivity experiments showed an excellent selectivity of 57.2 in a CO 2 /N 2 mixture (15:85). The Isosteric Adsorption Heat (Q st ) level of 15.9–23.8 kJ/mol confirmed low regeneration energy, thus making this material highly promising for practical applications.

Results in EngineeringVol. 27
University of Science and Technology Liaoning (CN), City University of Hong Kong (HK), Shenzhen Polytechnic University (CN), Chinese Academy of Sciences (CN), Guangzhou Institute of Energy Conversion (CN)
Responsible consumption and production
Openalex Percentile: Top 10%
Carbon Dioxide Capture Technologies
2.85
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.