尿素辅助一步热解合成大孔碳气凝胶/MgO复合材料的快速磷酸盐回收。

IF 3.9 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Xiaojun Ma, , , Yan Kong, , , Haitao Feng, , , Jie Jia, , , Zuhai Hu, , , Jiao He, , , Liang Jiang, , , Yongjuan Chen*, , and , Jiaqiang Wang*, 
{"title":"尿素辅助一步热解合成大孔碳气凝胶/MgO复合材料的快速磷酸盐回收。","authors":"Xiaojun Ma,&nbsp;, ,&nbsp;Yan Kong,&nbsp;, ,&nbsp;Haitao Feng,&nbsp;, ,&nbsp;Jie Jia,&nbsp;, ,&nbsp;Zuhai Hu,&nbsp;, ,&nbsp;Jiao He,&nbsp;, ,&nbsp;Liang Jiang,&nbsp;, ,&nbsp;Yongjuan Chen*,&nbsp;, and ,&nbsp;Jiaqiang Wang*,&nbsp;","doi":"10.1021/acs.langmuir.5c03529","DOIUrl":null,"url":null,"abstract":"<p >Addressing global phosphorus scarcity and eutrophication, MgO-based adsorbents face challenges of slow kinetics and low active-site utilization. In this study, a waste biomass-derived carbon aerogel (CA) was used as a support for a one-step pyrolysis method, simultaneously constructing a porous structure and achieving high-dispersion MgO loading. Results showed a maximum adsorption capacity of 399.8 mg P/g. Kinetic studies indicated 165.4 mg P/g adsorbed within 5 min, with 90% saturation achieved within 40 min. The Pseudo-second-order kinetic constants increased 11-fold compared to commercial MgO. By integrating experiments, machine learning (ML), and density functional theory (DFT), a multiscale investigation revealed the synergistic effect between MgO and the carbon aerogel support. It was demonstrated that the rapid adsorption kinetics originated from the macroporous structure of the support rather than a high specific surface area. Furthermore, urea participation during pyrolysis modulated the pyridinic-N content of the CA, thereby modifying the pH adaptability of the material. Collectively, this study provides a foundation for reusing waste biochar and designing high-performance phosphate adsorbents.</p>","PeriodicalId":50,"journal":{"name":"Langmuir","volume":"41 41","pages":"27868–27879"},"PeriodicalIF":3.9000,"publicationDate":"2025-10-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Urea-Assisted One-Step Pyrolytic Synthesis of Macroporous Carbon Aerogel/MgO Composites for Rapid Phosphate Recovery\",\"authors\":\"Xiaojun Ma,&nbsp;, ,&nbsp;Yan Kong,&nbsp;, ,&nbsp;Haitao Feng,&nbsp;, ,&nbsp;Jie Jia,&nbsp;, ,&nbsp;Zuhai Hu,&nbsp;, ,&nbsp;Jiao He,&nbsp;, ,&nbsp;Liang Jiang,&nbsp;, ,&nbsp;Yongjuan Chen*,&nbsp;, and ,&nbsp;Jiaqiang Wang*,&nbsp;\",\"doi\":\"10.1021/acs.langmuir.5c03529\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Addressing global phosphorus scarcity and eutrophication, MgO-based adsorbents face challenges of slow kinetics and low active-site utilization. In this study, a waste biomass-derived carbon aerogel (CA) was used as a support for a one-step pyrolysis method, simultaneously constructing a porous structure and achieving high-dispersion MgO loading. Results showed a maximum adsorption capacity of 399.8 mg P/g. Kinetic studies indicated 165.4 mg P/g adsorbed within 5 min, with 90% saturation achieved within 40 min. The Pseudo-second-order kinetic constants increased 11-fold compared to commercial MgO. By integrating experiments, machine learning (ML), and density functional theory (DFT), a multiscale investigation revealed the synergistic effect between MgO and the carbon aerogel support. It was demonstrated that the rapid adsorption kinetics originated from the macroporous structure of the support rather than a high specific surface area. Furthermore, urea participation during pyrolysis modulated the pyridinic-N content of the CA, thereby modifying the pH adaptability of the material. Collectively, this study provides a foundation for reusing waste biochar and designing high-performance phosphate adsorbents.</p>\",\"PeriodicalId\":50,\"journal\":{\"name\":\"Langmuir\",\"volume\":\"41 41\",\"pages\":\"27868–27879\"},\"PeriodicalIF\":3.9000,\"publicationDate\":\"2025-10-09\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Langmuir\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acs.langmuir.5c03529\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Langmuir","FirstCategoryId":"92","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.langmuir.5c03529","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

摘要

为解决全球磷短缺和富营养化问题,基于mgo的吸附剂面临着动力学慢和活性位点利用率低的挑战。本研究以废弃生物质衍生的碳气凝胶(CA)为载体,采用一步热解法,在构建多孔结构的同时,实现了高分散的MgO负载。结果表明,其最大吸附量为399.8 mg P/g。动力学研究表明,5 min内吸附165.4 mg P/g, 40 min内达到90%的饱和。伪二阶动力学常数比工业MgO提高了11倍。通过综合实验、机器学习(ML)和密度泛函理论(DFT),一项多尺度研究揭示了MgO和碳气凝胶载体之间的协同效应。结果表明,快速吸附动力学源于载体的大孔结构,而不是高比表面积。此外,热解过程中尿素的参与调节了CA的吡啶- n含量,从而改变了材料的pH适应性。本研究为废弃生物炭的资源化利用和高性能磷酸盐吸附剂的设计提供了基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Urea-Assisted One-Step Pyrolytic Synthesis of Macroporous Carbon Aerogel/MgO Composites for Rapid Phosphate Recovery

Urea-Assisted One-Step Pyrolytic Synthesis of Macroporous Carbon Aerogel/MgO Composites for Rapid Phosphate Recovery

Addressing global phosphorus scarcity and eutrophication, MgO-based adsorbents face challenges of slow kinetics and low active-site utilization. In this study, a waste biomass-derived carbon aerogel (CA) was used as a support for a one-step pyrolysis method, simultaneously constructing a porous structure and achieving high-dispersion MgO loading. Results showed a maximum adsorption capacity of 399.8 mg P/g. Kinetic studies indicated 165.4 mg P/g adsorbed within 5 min, with 90% saturation achieved within 40 min. The Pseudo-second-order kinetic constants increased 11-fold compared to commercial MgO. By integrating experiments, machine learning (ML), and density functional theory (DFT), a multiscale investigation revealed the synergistic effect between MgO and the carbon aerogel support. It was demonstrated that the rapid adsorption kinetics originated from the macroporous structure of the support rather than a high specific surface area. Furthermore, urea participation during pyrolysis modulated the pyridinic-N content of the CA, thereby modifying the pH adaptability of the material. Collectively, this study provides a foundation for reusing waste biochar and designing high-performance phosphate adsorbents.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Langmuir
Langmuir 化学-材料科学:综合
CiteScore
6.50
自引率
10.30%
发文量
1464
审稿时长
2.1 months
期刊介绍: Langmuir is an interdisciplinary journal publishing articles in the following subject categories: Colloids: surfactants and self-assembly, dispersions, emulsions, foams Interfaces: adsorption, reactions, films, forces Biological Interfaces: biocolloids, biomolecular and biomimetic materials Materials: nano- and mesostructured materials, polymers, gels, liquid crystals Electrochemistry: interfacial charge transfer, charge transport, electrocatalysis, electrokinetic phenomena, bioelectrochemistry Devices and Applications: sensors, fluidics, patterning, catalysis, photonic crystals However, when high-impact, original work is submitted that does not fit within the above categories, decisions to accept or decline such papers will be based on one criteria: What Would Irving Do? Langmuir ranks #2 in citations out of 136 journals in the category of Physical Chemistry with 113,157 total citations. The journal received an Impact Factor of 4.384*. This journal is also indexed in the categories of Materials Science (ranked #1) and Multidisciplinary Chemistry (ranked #5).
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信