(314b) Reaction Path Analysis of the Total Oxidation of Propane Over a Cuo-CeO2/γ-Al2O3 Catalyst by Means of Temporal Analysis of Products (TAP)

Abstract

Total oxidation of volatile organic compounds using metal oxide catalysts has become a necessary end-of-pipe process in order to reduce VOCs emissions. A TAP reactor is applied to investigate the mechanism and kinetics of propane oxidation over a CuO-CeO₂/γ-Al₂O₃ catalyst. Both single-pulse and multi-pulse experiments are performed between 523 and 923 K using various feeds: pure C₃H₈, O₂ and CO₂ next to mixtures C₃H₈/O₂ and C₃H₈/CO₂. At 523 and 573 K propane interacts irreversibly with the oxidized catalyst, while no interaction with dioxygen is observed. From 623 K on both reactant responses show two maxima, indicating reversible interaction with the catalyst. At all temperatures, CO₂ is the main reaction product both in the absence and presence of O₂.
NoCO is formed and only small amounts of propene are detected. H₂O adsorbs strongly on the catalyst surface. Part of the formed CO₂ also remains adsorbed on the catalyst up to 923 K. Despite this strong CO₂ adsorption, the propane conversion at 623 K is not decreasing as the catalyst is submitted to a series of experiments. Adding CO₂ to the propane feed is even increasing the catalyst activity.

1.              Introduction

Given the ever growing environmental concerns, volatile organic compounds (VOCs) should be eliminated as much as possible before releasing waste gases into the atmosphere. According to Spivey [1], catalytic oxidation is one of the most effective technologies for the destruction of VOCs. Supported noble metal catalysts have been established as efficient catalysts for this destruction. However, metal oxide catalysts appear to be a good economic alternative, in particular CuO-CeO₂/γ-Al₂O₃ [2].

In this research, the total oxidation of propane as model molecule for VOCs is studied over a CuO-CeO₂/γ-Al₂O₃ catalyst using the TAP reactor [3] to gain insight into the details of the reaction mechanism.

2.              Experimental

The total oxidation of propane was studied, performing single-pulse and multi-pulse experiments on 50 mg of a CuO-CeO₂/γ-Al₂O₃ catalyst. This amount of catalyst corresponds to 6.61 10¹⁹ O atoms based on both CuO and CeO₂ present in the catalyst. This amount is assumed to be an upper limit for the total number of exchangeable O atoms. The experiments are carried out with different feeds: C₃H₈/Kr (90/10), O₂/Ar (50/50), CO₂/Ar (50/50), C₃H₈/Kr + O₂ (O₂/C₃H₈ ratio of 5) and C₃H₈/Kr + CO₂ (CO₂/C₃H₈ ratio of 5) and with varying temperatures in steps of 50 K between 523 and 923 K. The fresh catalyst samples are first heated to reaction temperature with a ramp of 5 K/min under vacuum. Subsequently, the catalyst is pretreated with multi-pulses of O₂ until a constant level of the oxygen response is obtained.

3.              Results and discussion

The analysis of the propane and dioxygen pulse responses at 523 and 573 K demonstrates that propane is irreversibly interacting with the oxidized catalyst, while dioxygen does not interact. As temperature is increasing, the responses start to show two local maxima. The first corresponds to a fast adsorption while the second is caused by slow desorption.

CO₂ is the most important product at all temperatures during C₃H₈ oxidation, while only very small amounts of C₃H₆ are detected. Neither H₂O, nor CO can be observed during single-pulse experiments, although H₂O is sporadically detected on a scan, indicating that desorption takes place. The same products are present when a C₃H₈/O₂ mixture is fed into the reactor, but in this case higher propane conversions are obtained. Figure 1 shows the propane conversion over 50 mg of catalyst at 623 K for three different feeds as a function of the ratio between the O consumption by reaction and the O initially present in the oxidized catalyst as CuO and CeO₂. When pure propane is pulsed, the conversion is lower and decreases rapidly from 25% to around 3%. This indicates that reduction of the catalyst is taking place by using O atoms from the catalyst to form the oxidation products. Feeding dioxygen together with propane in a stoichiometric ratio of 5 to 1 causes a much less pronounced decrease in the conversion levelling off towards a value of 30%. This observation indicates that the dioxygen present in the feed is consumed by the catalyst in order to re-oxidize the sites that were reduced due to propane. However, since the average O₂ conversion is only 10%, not all sites that were reduced during propane oxidation are re-oxidized by gaseous O₂, leading to a decrease in the catalyst activity.

Figure 1: Comparison of the propane conversion at 623 K as a function of the oxygen consumption during reaction for three different feeds. When pure C₃H₈ is fed, the activity of the fresh catalyst is compared with the activity of the same catalyst sample that was subjected to reduction-oxidation experiments for 5 and 7 days: ♦ pure C₃H₈-fresh catalyst, ▲ pure C₃H₈-catalyst after use for 5 days, Δ pure C₃H₈-catalyst after use for 7 days, ● C₃H₈/O₂ (ratio 1:5) and * C₃H₈/CO₂ (ratio 1:5)

The most surprising observation is that between 523 and 723 K the CO₂ yield remains very low even if three times more catalyst is present in the reactor. Moreover, at these lower temperatures the CO₂ yield does not increase when a C₃H₈/O₂ mixture is fed instead of pure propane although the conversion is higher in the first case. Based on these observations, it is expected that part of the CO₂ formed during reaction remains adsorbed on the catalyst surface. In order to investigate this issue into more detail, CO₂ mixed with Ar is sent over the oxidized catalyst at different temperatures. At the lower temperatures (523-723 K), CO₂ is strongly interacting with the catalyst since only a small amount is detected at the outlet. From 773 K on, considerably more CO₂ is reaching the reactor outlet until at 923 K almost no CO₂ adsorption is observed anymore.

Because CO₂ is staying adsorbed on the catalyst during reaction with C₃H₈ or C₃H₈/O₂ at low temperatures, a possible change in activity can be expected if a catalyst sample is used in the TAP for a longer period of time. However, the catalyst activity is not influenced by this CO₂ adsorption as is illustrated on Figure 1 (triangles), where the propane conversion at 623 K is presented at different times after a fresh catalyst sample was loaded into the reactor. Even if experiments involving reduction or total oxidation and subsequent re-oxidation are performed for 7 days on the same catalyst sample, no significant difference in propane conversion can be observed. When CO₂ is added to the pure propane feed, the conversion at 623 K becomes significantly higher compared to when pure propane is fed into the reactor and initially reaches a level comparable to the conversion with a stoichiometric C₃H₈/O₂ mixture (see Figure 1).

4.              Conclusions

The CuO-CeO₂/γ-Al₂O₃ catalyst performs well as a total oxidation catalyst since no CO and almost no C₃H₆ is detected during reaction with C₃H₈ or C₃H₈/O₂ between 523 K and 923 K. However, the catalyst interacts very strongly with CO₂, leading to unclosed carbon balances at lower temperatures. This irreversible CO₂ adsorption on the catalyst at low temperatures does not affect the activity.

Acknowledgements

This work was performed in the framework of a Concerted Research Action (GOA) financed by the
Ghent University.

References

[1]      J.J. Spivey, Ind. Chem. Res. 26, 1987, 2165-2180

[2]      C.R. Jung, J. Han, S.W.
Nam, T.-H. Lim, S.-A. Hong, H.-I. Lee, Catal. Today 93-95, 2004, 183-190

[3]      J.T. Gleaves, J.R. Ebner, T.C. Kuechler, Catal. Rev. Sci.
Eng. 30, 1988, 49-116