Suppr超能文献

壳聚糖水热碳化制备吸附剂的合成、表征及一氧化碳吸附性能

Synthesis, Characterization, and CO Uptake of Adsorbents Prepared by Hydrothermal Carbonization of Chitosan.

作者信息

Chagas José A O, Crispim Gustavo O, Pinto Bianca P, San Gil Rosane A S, Mota Claudio J A

机构信息

Instituto de Química, Universidade Federal do Rio de Janeiro, Av. Athos da Silveira Ramos 149, CT Bl A, Cidade Universitária, Rio de Janeiro, RJ 21941-909, Brazil.

Escola de Química, Universidade Federal do Rio de Janeiro, Av. Athos da Silveira Ramos 149, CT Bl E, Cidade Universitária, Rio de Janeiro, RJ 21941-909, Brazil.

出版信息

ACS Omega. 2020 Nov 3;5(45):29520-29529. doi: 10.1021/acsomega.0c04470. eCollection 2020 Nov 17.

Abstract

Chitosan, a heteropolysaccharide obtained from the N-deacetylation of chitin, has stood out as a raw material to produce CO adsorbents. In this work, we report the hydrothermal carbonization (HTC) of chitosan for different times and the potential of the materials for CO adsorption. Elemental analysis indicated that the carbon weight content increases, whereas the relative amount of oxygen atoms decreases upon increasing the time of HTC. The relative nitrogen content was almost constant, indicating that HTC did not lead to significant loss of nitrogenated compounds. FTIR and C MAS/NMR spectra suggest that the structure of the sorbents becomes more aromatic with the increase of HTC time. The thermal properties of HTC materials were similar to that of chitosan, whereas their basicity was less compared to that of the parent chitosan. SEM images did not show significant porosity, which was confirmed by the BET area of the materials, around 2 m·g, similar to that of the parent chitosan. The materials were tested for CO capture at 25 °C and 1 bar; the HTC chitosan adsorbents showed CO uptakes about 4-fold higher than that of the parent chitosan. The adsorption process was better described by the Freundlich isotherm and the pseudo-second-order kinetic model.

摘要

壳聚糖是一种通过几丁质的N-脱乙酰作用得到的杂多糖,作为生产一氧化碳吸附剂的原料脱颖而出。在这项工作中,我们报告了壳聚糖在不同时间的水热碳化(HTC)以及所得材料对一氧化碳的吸附潜力。元素分析表明,随着水热碳化时间的增加,碳的重量含量增加,而氧原子的相对含量减少。相对氮含量几乎保持不变,这表明水热碳化不会导致含氮化合物的大量损失。傅里叶变换红外光谱(FTIR)和碳-13固体核磁共振(C MAS/NMR)光谱表明,随着水热碳化时间的增加,吸附剂的结构变得更加芳香。水热碳化材料的热性能与壳聚糖相似,但其碱性比母体壳聚糖小。扫描电子显微镜(SEM)图像未显示出明显的孔隙率,这通过材料的比表面积(约2 m²·g⁻¹)得到证实,与母体壳聚糖相似。在25℃和1巴的条件下对这些材料进行了一氧化碳捕获测试;水热碳化壳聚糖吸附剂对一氧化碳的吸附量比母体壳聚糖高出约4倍。吸附过程用弗伦德利希等温线和伪二级动力学模型能更好地描述。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2925/7676339/799a2d2a73e3/ao0c04470_0002.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验