TY - JOUR
T1 - Towards eco-friendly biofuel design
T2 - Atmospheric transformation and divergent ecological risk assessment of dimethylbutanol isomers
AU - Wang, Zhi Meng
AU - Yu, Wan Ying
AU - Ni, Shuang
AU - Chi, Tai Xing
AU - Bai, Feng Yang
AU - Zhang, Ke
AU - Zhang, Xiu Hui
AU - Zhao, Zhen
N1 - Publisher Copyright:
© 2026 Elsevier Ltd.
PY - 2026/9/20
Y1 - 2026/9/20
N2 - 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.
AB - 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.
KW - Atmospheric oxidation
KW - Branched alcohols
KW - Environmental risk assessment
KW - MS-CVT/SCT
KW - Reaction mechanism
UR - https://www.scopus.com/pages/publications/105048461792
U2 - 10.1016/j.jclepro.2026.149324
DO - 10.1016/j.jclepro.2026.149324
M3 - Article
AN - SCOPUS:105048461792
SN - 0959-6526
VL - 576
JO - Journal of Cleaner Production
JF - Journal of Cleaner Production
M1 - 149324
ER -