跳到主要导航 跳到搜索 跳到主要内容

Towards eco-friendly biofuel design: Atmospheric transformation and divergent ecological risk assessment of dimethylbutanol isomers

  • Zhi Meng Wang
  • , Wan Ying Yu
  • , Shuang Ni
  • , Tai Xing Chi
  • , Feng Yang Bai*
  • , Ke Zhang
  • , Xiu Hui Zhang*
  • , Zhen Zhao
  • *此作品的通讯作者
  • Institute of Catalysis for Energy and Environment
  • Shenyang Normal University
  • State Key Laboratory of Environment Characteristics and Effects for Near-space
  • Beijing Institute of Technology
  • College of Science
  • China University of Petroleum - Beijing

科研成果: 期刊稿件 › 文章 › 同行评审

摘要

Branched saturated higher alcohols such as 3,3-dimethyl-1-butanol (3,3DM1ButOH) and 3,3-dimethyl-2-butanol (3,3DM2ButOH) are promising oxygenated biofuel additives, yet their atmospheric transformation pathways and associated ecological risks remain poorly constrained. Here, we integrate density functional theory with multi-structural canonical variational transition state theory including small-curvature tunneling to elucidate the ·OH-initiated oxidation mechanisms and kinetics of both isomers over atmospherically relevant conditions. Four distinct H-abstraction channels are identified for each alcohol, with reactivity governed by hydroxyl position: the β -secondary H in 3,3DM1ButOH and the α-carbinol H in 3,3DM2ButOH dominate abstraction. At 298 K, computed total rate coefficients—5.29 × 10−12 cm3 molecule−1 s−1 (3,3DM1ButOH) and 1.07 × 10−11 cm3 molecule−1 s−1 (3,3DM2ButOH)—agree well with experimental data and reveal that 3,3DM2ButOH reacts nearly twice as fast due to its activated α-hydrogen. Subsequent peroxy radical (RO2·) chemistry is mapped under varying NOx regimes: RO2· + NO dominates in polluted environments, yielding multifunctional carbonyls (e.g., aldehydes, enols, ketones) and organic peroxynitrite (ROONO), while RO2· + HO2· and RO2· + RO2· pathways under low-NOx conditions produce hydroperoxides (ROOH) and dimeric products. Critically, environmental risk assessment using EPA-based toxicity models reveals divergent hazard trajectories: H-shift-driven autoxidation channels amplify developmental and aquatic toxicity, whereas radical termination via RO2· + HO2·/RO2· yields readily biodegradable, low-toxicity products. The RO2· + NO route exhibits mixed risk outcomes. Overall, low-NOx conditions mitigate integrated ecological risk despite comparable degradation rates. These findings bridge atmospheric chemical mechanisms with ecological risk assessment, providing a scientific foundation for the development of eco-friendlier biofuel additives with reduced environmental hazards.

源语言英语
期刊论文编号149324
期刊Journal of Cleaner Production
卷576
DOI
出版状态已出版 - 20 9月 2026

学术指纹

探究 'Towards eco-friendly biofuel design: Atmospheric transformation and divergent ecological risk assessment of dimethylbutanol isomers' 的科研主题。它们共同构成独一无二的学术指纹。

引用此