Data di Pubblicazione:
2017
Citazione:
Kinetic Analysis and Reactor Design of Ethanol Steam Reforming / A. Tripodi, M. Compagnoni, G. Ramis, I.G. Rossetti. ((Intervento presentato al convegno Europacat tenutosi a Firenze nel 2017.
Abstract:
A set of kinetic tests for ethanol steam reforming have been performed and were used as basis for kinetic modelling of the reaction. We performed 25 tests varying temperature, space velocity and water/ethanol ratio according to a composite design of experiments. The results were quantitatively used to understand the parametric dependence of conversion and selectivity on the selected variables, including statistical analysis. Microkinetic modelling followed, specifically focusing on the steps that predict by-products formation. At difference with literature we also interpreted coke accumulation over catalyst surface. Literature data were also modelled to check for consistency and versatility of the proposed kinetic scheme.
1. Scope
An experimental kinetic investigation has been carried out for ethanol steam reforming (ESR). The selected catalyst was a 9 wt% K2O-10 wt% Ni/ZrO2 sample prepared by flame pyrolysis, which revealed particularly active and stable for this application based on previous investigations of the group. Ethanol conversion, selectivity to the main possible byproducts (methane, ethylene and acetaldehyde), hydrogen productivity and the CO/CO2 ratio, as a measure of the contribution of the water gas shift reaction, were correlated to the experimental variables chosen. They were temperature, water/ethanol ratio and space velocity explored in the variable space by means of a central composite experimental design. The parametric dependence of the reaction outcomes helped the qualitative assessment of the best operating conditions and suggested hypotheses on the reaction mechanism. A more quantitative parametric analysis was carried out by multivariate analysis.
Particularly dramatic experimental conditions have been adopted in order to highlight the formation and further evolution of possibly critical intermediates, such as ethylene and acetaldehyde. Indeed, to keep ethanol and intermediates conversion below 100% at least at 550°C to guarantee coke-free operation, the space velocity and feed dilution were increased.
An extended microkinetic model has been proposed for the ethanol steam reforming reaction that includes kinetic steps for the formation of important byproducts such as ethylene, acetaldehyde and coke. The model, initially drawn on our own experimental data, was also validated against literature data collected over a different catalytic system and without the presence of the selected byproducts.
2. Results and discussion
The catalyst was tested under the following experimental conditions [1]:
Min Max
T (°C) 550 650
Catalyst (mg) 26 132
EtOH : H2O (mol/mol) 1 : 5 1 : 3
GHSV (h-1) 25000 125000
An increase of temperature did not adequately improved H2 selectivity, whereas the water/ethanol ratio was an effective parameter to push forward H2 productivity. The reforming reactions of ethanol and of acetaldehyde/ethylene byproducts were dependent on the three parameters (kinetically controlled), whereas the CO/CO2 ratio was substantially independent on the space velocity, indicating that the water gas shift reaction reached a quasi-equilibrium value.
The data were elaborated by setting up a Matlab script for data regression. A Plug-flow reactor model was implemented, neglecting radial dispersion and back mixing. Isothermal operation was assumed and checked experimentally, due to the very low amount of catalyst, diluted in SiC. The same model was also implemented in the Aspen Plus process simulator, obtaining comparable results.
The proposed micrikinetic model, sketched in Figure 1, gave very straightforward predictions of catalyst performance for the literature data: in this case the lump sum of all the square residues (calculated vs. tabulated mol fractions) was 2.88 x 10-2 over a dataset
Tipologia IRIS:
14 - Intervento a convegno non pubblicato
Elenco autori:
A. Tripodi, M. Compagnoni, G. Ramis, I.G. Rossetti
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