Abstract

In this study, the production of synthesis gases has been purposed under between 250oC - 700oC and 1 - 2 bars pressures. The research was conducted over a commercial BASF catalyst and a laboratory prepared catalyst. The catalyst has a content of different substances including basically NiO/Al2O3 and some additionals (Ca, Mg, Cr, Si). The experimental measurements were carried out within a recently developed experimental equipment which can be operated up to 1200o and 1 to 3 bars pressures. The study was conducted over a commercial BASF catalyst and a laboratory prepared catalyst under different ethanol/water ratios, temperatures, and catalyst loads. Under the condition when ethanol/water ratios were decreased from 1/2 to 1/10, it was observed that hydrogen ratios increased in exit gas composition of the reactor. With increments in catalyst loads from 1 to 5 grammes, hydrogen ratios in exit gas composition gradually increased. Reaction of ethanol-steam reforming started nearly at 300oC, and when temperature increments continued further up to 700oC, hydrogen yields in exit gas compositions of the reactor increased significantly to a range of 70% - 80%. In the case of using commercial BASF catalyst, hydrogen ratios in exit gas composition were found slightly higher than laboratory prepared catalyst. According to our observations, life time of laboratory prepared catalyst was found higher than the commercial BASF catalyst. In this study which kinetic measurements were applied, some kinetic parameters of ethanol-steam reaction were calculated. The mean activation energy of ethanol consumptions at 573oK - 973oK was found as 26.87 kJ/mol, approximately. All kinetic measurements were analyzed with a first order reaction rate model. In this study, some diffusion limitations existed, however, overall reaction was chemically controlled.

Highlights

  • Due to high demand in energy consumption and the recent improvements in fuel cell technology, it increases the synthesis gas production requirements from the different fuel sources

  • Hydrogen production yields were investigated at different EtOH/water ratios and at different temperatures with ethanol-water vapour process over a commercial BASF and a laboratory prepared catalyst

  • Some kinetic parameters related to ethanol-steam reforming reaction were determined at different temperature conditions and at different catalyst loads with different ethanol/water feed ratios

Read more

Summary

Introduction

Due to high demand in energy consumption and the recent improvements in fuel cell technology, it increases the synthesis gas production requirements from the different fuel sources. It was demonstrated that ceria supported catalyst were significantly active and selective for hydrogen production by steam reforming of ethanol. A. Akande et al [28] studied kinetic modeling of hydrogen production by the catalytic reforming of crude ethanol over a Ni-Al2O3 catalyst in a packed bed tubular reactor. The findings from this study show that syngas production from methane dry reforming over ceria-supported cobalt catalyst is significantly influenced by the variation in the partial pressure of the reactants.Their catalytic activity test shows that highest CO2 and CH4 conversions were obtained at CH4 partial pressure of 45 and 25 kPa. Production of hydrogen from steam reforming of ethanol over LaNiO3 and LaNiO3/CeSiO2 oxide types catalysts was studied by A. At higher temperatures more than 700 ̊C, some increments in production rate of CO were detected and a small decrement in H2 rate and some decrements in CO2 rate have been observed

Experimental System
The Composition of the Commercial BASF Catalyst and Catalyst Test Studies
The Composition of the Laboratory Prepared Catalyst and Catalyst Test Studies
Results and Discussions
Conclusions

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.