Institute of Biogeochemistry and Pollutant Dynamics (IBP), Department of Environmental Systems Science, ETH Zurich, 8092 Zurich, Switzerland.
Environ Sci Process Impacts. 2017 Apr 19;19(4):507-516. doi: 10.1039/c6em00646a.
The rate constant for the reaction between furfuryl alcohol (FFA) and singlet oxygen (O) in aqueous solution was measured as a function of temperature, pH and salt content employing both steady-state photolysis (β value determination) and time-resolved singlet oxygen phosphorescence methods. The latter provided more precise and reproducible data. The reaction rate constant, k, had a relatively small temperature dependence, no pH dependence and showed a small increase in the presence of high salt concentrations (+19% with 1 M NaCl). A critical review of the available literature suggested that the widely used value of 1.2 × 10 M s is likely overestimated. Therefore, we recommend the use of 1.00 × 10 M s for reactions performed in low ionic strength aqueous solutions (freshwater) at 22 °C. Furthermore, corrections are provided that should be applied when working at higher or lower temperatures, and/or at high salt concentrations (seawater).
采用稳态光解(β 值测定)和时间分辨单重态氧磷光法测量了糠醇(FFA)与单重态氧(O)在水溶液中的反应速率常数随温度、pH 值和盐含量的变化。后者提供了更精确和可重复的数据。反应速率常数 k 对温度的依赖性相对较小,对 pH 值没有依赖性,并且在高盐浓度下略有增加(在 1 M NaCl 下增加 19%)。对现有文献的批判性回顾表明,广泛使用的 1.2×10 M s 值可能被高估。因此,我们建议在 22°C 下在低离子强度水溶液(淡水)中进行反应时使用 1.00×10 M s。此外,还提供了在较高或较低温度以及/或高盐浓度(海水)下工作时应应用的校正值。