کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1733757 | 1016145 | 2012 | 15 صفحه PDF | دانلود رایگان |
The thermal decomposition of methyl decanoate (MD) was studied in a bench-scale pyrolysis set-up equipped with a dedicated on-line analysis section including a GC × GC-FID/(TOF-MS). This analysis section enables quantitative and qualitative on-line analyses of the entire reactor effluent with high level of detail including measurement of formaldehyde and water. The reactor temperature was varied from 873 K to 1123 K at a fixed pressure of 1.7 bar and a fixed residence time of 0.5 s, for both high (10molN2/molMD) and low (0.6molN2/molMD) nitrogen dilution. Thus covering a wide conversion range in both dilution regimes. In these experiments, significant amounts of large linear olefins and unsaturated esters were observed at lower temperatures, the amounts of which decreased at higher temperatures in favor of permanent gasses (CO, CO2, CH4) and light olefins. At the highest temperatures more than 5 wt% of mono-aromatic and poly-aromatic components were observed. The acquired dataset was used to validate 3 recently published microkinetic models which were developed to model oxidation and/or pyrolysis of methyl decanoate. The results showed that these models accurately predict the product distribution, although important discrepancies were observed for some major products such as certain unsaturated esters, CO2 and H2O. Reaction path analyses and CBS-QB3 quantum-chemical calculations are presented and discussed in order to explain the observed differences.
► New extensive experimental dataset for the pyrolysis of methyl decanoate in a tubular reactor.
► A dedicated separation section including on-line GC × GC allows to obtain quantitative data for over 150 components.
► High level ab-initio calculations for important reactions of the methyl decanoate decomposition.
► Identification of missing reactions/reaction families/inaccurate kinetics in the presently available kinetic models.
Journal: Energy - Volume 43, Issue 1, July 2012, Pages 146–160