Centre National de la Recherche Scientifique-Institut National des Sciences de l'Ingénierie et des Systèmes, Institut de Combustion, Aérothermique, Réactivité, Environnement, 1C Avenue de la Recherche Scientifique, CEDEX 2, 45071 Orléans, France.
Collegium Sciences et Techniques, Rue de Chartres, Université d'Orléans, 45100 Orléans, France.
Molecules. 2021 Nov 26;26(23):7174. doi: 10.3390/molecules26237174.
In the present study, we investigated the oxidation of 2500 ppm of di-n-butyl ether under fuel-rich conditions (φ = 2) at low temperatures (460-780 K), a residence time of 1 s, and 10 atm. The experiments were carried out in a fused silica jet-stirred reactor. Oxidation products were identified and quantified in gas samples by gas chromatography and Fourier transform infrared spectrometry. Samples were also trapped through bubbling in cool acetonitrile for high-pressure liquid chromatography (HPLC) analyses. 2,4-dinitro-phenylhydrazine was used to derivatize carbonyl products and distinguish them from other isomers. HPLC coupled to high resolution mass spectrometry (Orbitrap Q-Exactive) allowed for the detection of oxygenated species never observed before, i.e., low-temperature oxidation products (CHO, CHO, and CHO,) and species that are more specific products of atmospheric oxidation, i.e., CHO, CHO, CHO, and CHO. Flow injection analyses indicated the presence of high molecular weight oxygenated products ( > 550). These results highlight the strong similitude in terms of classes of oxidation products of combustion and atmospheric oxidation, and through autoxidation processes. A kinetic modeling of the present experiments indicated some discrepancies with the present data.
在本研究中,我们在富燃料条件(φ=2)、低温(460-780 K)、停留时间为 1 秒和 10 大气压下,研究了 2500 ppm 的二丁醚的氧化。实验在熔融石英射流搅拌反应器中进行。通过气相色谱和傅里叶变换红外光谱法对气体样品中的氧化产物进行了鉴定和定量分析。通过在低温乙腈中鼓泡,也对样品进行了捕获,用于高压液相色谱(HPLC)分析。2,4-二硝基苯肼用于衍生化羰基产物,并将其与其他异构体区分开来。HPLC 与高分辨率质谱(Orbitrap Q-Exactive)联用,可检测到以前从未观察到的含氧物种,即低温氧化产物(CHO、CHO 和 CHO),以及更特定的大气氧化产物,即 CHO、CHO、CHO 和 CHO。流动注射分析表明存在高分子量含氧产物(>550)。这些结果突出了燃烧和大气氧化过程中通过自动氧化途径,在氧化产物类别方面的强相似性。对本实验的动力学建模表明,与现有数据存在一些差异。