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Experimental study of CO(2) capture by nanoparticle-enhanced 2-amino-2-methyl-1-propanol aqueous solution

2-Amino-2-methyl-1-propanol (AMP) is often used as a moderator to enhance the CO(2) capture capacity of absorbents due to its unique spatial site resistance structure, and relatively few studies have been conducted on the enhancement of AMP aqueous solutions by nanoparticles for CO(2) capture. In or...

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Detalles Bibliográficos
Autores principales: Zhang, Qiuli, Ning, Zhongyi, Li, Xuelian, Ning, Xiaogang, Wu, Fan, Zhou, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10652185/
https://www.ncbi.nlm.nih.gov/pubmed/38020032
http://dx.doi.org/10.1039/d3ra06767j
Descripción
Sumario:2-Amino-2-methyl-1-propanol (AMP) is often used as a moderator to enhance the CO(2) capture capacity of absorbents due to its unique spatial site resistance structure, and relatively few studies have been conducted on the enhancement of AMP aqueous solutions by nanoparticles for CO(2) capture. In order to investigate the effect of nanoparticles on the CO(2) capture performance of AMP aqueous solution, different nanofluids were formulated in this paper using a two-step method, and a bubbling reactor and an oil bath were used as the experimental setup for absorption/desorption, and through comparative experiments, it was found that the type of nanoparticles, the solid content, and the different parameters have great influences on the CO(2) absorption load and desorption rate. The experimental results show that the addition of TiO(2) nanoparticles to the AMP base solution can accelerate the absorption–desorption mass transfer rate of CO(2), and there exists an optimal solid content of 1 g L(−1) (±1.0%, ±2.5%); after multiple absorption–desorption experiments, good cycling performance can still be achieved. The experimental results of the nanofluid-promoted mass transfer mechanism are also illustrated and analyzed in this paper.