In-situ carbonate mineral coupling by hydrothermal carbonization: a strategy for enhanced hydrochar stability and long-term carbon sequestration

IF 7.5 1区 工程技术 Q2 ENERGY & FUELS
Fuel Pub Date : 2025-06-13 DOI:10.1016/j.fuel.2025.135709
Xin Luo , Xiangjun Pei , Xiaochao Zhang , Xiangrui He , Tao Liu , Xiaoye Dong
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Abstract

The development of effective carbon sequestration materials is crucial for mitigating climate change. This study introduces a novel one-step hydrothermal carbonization (HTC) strategy to enhance hydrochar carbon sequestration by in-situ coupling carbonate minerals (CaCO3 and MgCO3). Unlike traditional biochar-mineral coupling methods, which suffer from poor interaction and uneven mineral distribution, this approach enables uniform mineral nucleation and crystalline growth within the hydrochar matrix. The result shows that the hydrothermal environment facilitates effective ion dispersion and the formation of a stable organic–inorganic composite, with functional groups like carboxyl and hydroxyl on the hydrochar surface promoting mineral nucleation. Mineral-coupled hydrochars exhibited significant improvements in carbon sequestration capacity compared to pristine hydrochar. Ca coupling resulted in a 69.9 % reduction in carbon loss rate under oxidative conditions, a 41.86 % increase in thermal stability, and a 63.86 % reduction in dissolved organic carbon (DOC). Mg coupling also enhanced stability, reducing carbon loss by 47.8 % and DOC by 54.5 %, although its thermal stability (R50 = 0.53) and mineral integration were less pronounced due to the formation of smaller, less crystalline MgCO3 particles. These improvements are attributed to the synergistic interaction between the carbon matrix and mineral phase, which reduces O-containing groups, enhances condensation, and forms a crystalline barrier. This work demonstrates that mineral coupling during HTC significantly enhances hydrochar stability and carbon retention, offering a scalable and sustainable solution for long-term carbon storage and negative-emission technologies.
热液碳化的原位碳酸盐矿物耦合:提高烃类稳定性和长期固碳的策略
开发有效的固碳材料对减缓气候变化至关重要。本研究提出了一种新的一步水热碳化(HTC)策略,通过原位耦合碳酸盐矿物(CaCO3和MgCO3)来增强烃类碳固存。传统的生物炭-矿物耦合方法相互作用差,矿物分布不均匀,与之不同的是,这种方法可以在碳氢化合物基质中实现均匀的矿物成核和晶体生长。结果表明,水热环境有利于离子有效分散,形成稳定的有机无机复合物,烃类表面羧基、羟基等官能团促进矿物成核。与原始碳氢化合物相比,矿物偶联碳氢化合物的固碳能力有显著提高。Ca偶联使氧化条件下的碳损失率降低了69.9%,热稳定性提高了41.86%,溶解有机碳(DOC)降低了63.86%。Mg偶联也增强了稳定性,减少了47.8%的碳损失和54.5%的DOC,尽管其热稳定性(R50 = 0.53)和矿物整合不太明显,因为形成了更小、更不结晶的MgCO3颗粒。这些改进是由于碳基体和矿物相之间的协同作用,减少了含o基团,增强了缩聚,形成了晶体屏障。这项研究表明,在HTC过程中,矿物偶联显著提高了碳氢化合物的稳定性和碳保留率,为长期碳储存和负排放技术提供了可扩展和可持续的解决方案。
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来源期刊
Fuel
Fuel 工程技术-工程:化工
CiteScore
12.80
自引率
20.30%
发文量
3506
审稿时长
64 days
期刊介绍: The exploration of energy sources remains a critical matter of study. For the past nine decades, fuel has consistently held the forefront in primary research efforts within the field of energy science. This area of investigation encompasses a wide range of subjects, with a particular emphasis on emerging concerns like environmental factors and pollution.
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