Enhanced CO<sub>2</sub> Capture and Utilization through Chemically and Physically Dual-Modified Amino Cellulose Aerogels Integrated with Microalgae-Immobilized Hydrogels

This study introduces a novel method for CO2 capture and utilization by integrating chemically and physically dual-modified amino cellulose aerogels with microalgae-immobilized silk fibroin/sodium alginate (SF/SA) composite hydrogels. The modified cellulose aerogels, enhanced with 3-(2-aminoethylamino)propyl-dimethoxymethylsilane (AEAPMDS) and fumed silica-polyethyleneimine (SiO2@PEI), exhibited significantly improved CO2 adsorption capacity, mechanical strength, and thermal stability compared to microcrystalline cellulose (MCC) aerogels. This modification addresses the limitations of traditional physical and chemical adsorption methods. The captured CO2 was effectively utilized by the microalgae embedded in the SF/SA hydrogel, leading to increased growth rates, improved carbon fixation efficiency, and reduced energy consumption during CO2 capture and storage. Temperature regulation was applied to optimize CO2 adsorption and desorption, demonstrating the system’s potential for air quality improvement and sustainable bioengineering applications, providing a new strategy to combat climate change.

Authors

Institutions

Publication Details

Journal
ACS ES&T Engineering
Published
2024-11-06
DOI
https://doi.org/10.1021/acsestengg.4c00597
Citations
11
Primary Topic
Carbon Dioxide Capture Technologies
Type
article
Field-Weighted Citation Impact
2.34

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Enhanced CO2 Capture and Utilization through Chemically and Physically Dual-Modified Amino Cellulose Aerogels Integrated with Microalgae-Immobilized Hydrogels

Zhaozhu Zheng, Sijie Li, David L. Kaplan, Xiaoqin Wang et al.
11 citations
ACS ES&T Engineering
Carbon Dioxide Capture Technologies
2.34
article

Enhanced CO2 Capture and Utilization through Chemically and Physically Dual-Modified Amino Cellulose Aerogels Integrated with Microalgae-Immobilized Hydrogels

Zhaozhu Zheng, Sijie Li, David L. Kaplan, Xiaoqin Wang, Gang Li, Jingjing Chang, Yibin Yu
article en
11 citations

Abstract

This study introduces a novel method for CO2 capture and utilization by integrating chemically and physically dual-modified amino cellulose aerogels with microalgae-immobilized silk fibroin/sodium alginate (SF/SA) composite hydrogels. The modified cellulose aerogels, enhanced with 3-(2-aminoethylamino)propyl-dimethoxymethylsilane (AEAPMDS) and fumed silica-polyethyleneimine (SiO2@PEI), exhibited significantly improved CO2 adsorption capacity, mechanical strength, and thermal stability compared to microcrystalline cellulose (MCC) aerogels. This modification addresses the limitations of traditional physical and chemical adsorption methods. The captured CO2 was effectively utilized by the microalgae embedded in the SF/SA hydrogel, leading to increased growth rates, improved carbon fixation efficiency, and reduced energy consumption during CO2 capture and storage. Temperature regulation was applied to optimize CO2 adsorption and desorption, demonstrating the system’s potential for air quality improvement and sustainable bioengineering applications, providing a new strategy to combat climate change.

ACS ES&T EngineeringVol. 5(2)
Tufts University (US), National Institute of Fashion Technology (IN), Soochow University (CN)
National Natural Science Foundation of China, National Key Research and Development Program of China
Openalex Percentile: Top 12%
Carbon Dioxide Capture Technologies
2.34
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.