首页> 外文期刊>Energy & fuels >Deciphering the Differential Influence of Organic Additives on Coal Fluidity Development: A First-Principles Investigation
【24h】

Deciphering the Differential Influence of Organic Additives on Coal Fluidity Development: A First-Principles Investigation

机译:解读有机添加剂对煤流动性发展的差异影响:一项初始化调查

获取原文
获取原文并翻译 | 示例
           

摘要

Formation of high-quality coke is essentially controlled by the development of the extended stability of the coal fluid phase during industrial carbonization processes. Stabilization of coal free radicals through hydrogenation leads to this development of coal fluidity. The donatable hydrogens are usually supplied by the donor hydrogen species formed through the thermal decomposition of a coal macromolecular network. In view of the limited reserve of the donor hydrogen species within a coal system, organic additives with characteristic hydrogen-donating ability are conventionally added to the system to maintain the desirable coal fluidity. However, the choice of compounds requires a clear understanding of their chemistry and associated reaction features. In this context, factors controlling hydrogen-donating properties of some organic donor hydrogen compounds are investigated herein within the framework of density functional theory. A mechanistic interpretation of the reaction of the compounds with the coal radical is offered. In addition to structural modification, the influence of the functional group, namely, the phenolic hydroxyl group, on the hydrogen-donating efficiency of the systems is validated through our calculations. The key role of molecular orbitals in facilitating the release of hydrogens from them is also elucidated. Thus, the work features an advanced understanding of a fundamental industrial process combining a detailed electronic description of the systems. The efficiency of a new compound to act as a superior hydrogen donor candidate is identified. The insights obtained are believed to help derive a rational understanding of the systems and structure–property relationships, which, in turn, can inspire future studies to engineer desired compounds with improved properties. The relevance of our findings to practical carbonization processes is also illustrated in the present work.
机译:高质量焦炭的形成基本上通过在工业碳化过程中发展煤流相的延长稳定性来控制。通过氢化稳定煤自由基导致这种煤流动性的发展。通过通过煤大分子网络的热分解形成的供体氢物质通常供应可提供的氢。鉴于煤系统内的供体氢物质的限量储备,常规添加具有特征氢捐助能力的有机添加剂以保持所需的煤流动性。然而,化合物的选择需要清楚地了解其化学和相关的反应特征。在这种情况下,在密度函数理论的框架内研究了控制一些有机供体氢化合物的氢化性质的因素。提供了将化合物与煤自由基反应的机械解释。除了结构改性外,通过我们的计算验证了官能团的影响,即酚羟基,酚羟基对系统的氢捐献效率进行了验证。分子轨道在促进它们中促进氢的关键作用也被阐明。因此,该工作具有对组合系统的详细电子描述的基本工业过程的高级理解。鉴定了新化合物用作优质氢供体候选物的效率。所获得的见解被认为有助于获得对系统和结构性质关系的合理理解,这反过来可以激发未来的研究,以改善具有改善的性质的所需化合物。我们对实际碳化过程的研究结果也在本作中说明。

著录项

  • 来源
    《Energy & fuels》 |2021年第5期|4053-4066|共14页
  • 作者单位

    Research and Development Tata Steel;

    School of Mathematical and Computational Sciences Indian Association for the Cultivation of Science Jadavpur;

    Research and Development Tata Steel;

    Research and Development Tata Steel;

    Research and Development Tata Steel;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号