Abstract

The kinetic rate parameters of a reaction rate model are usually estimated using reaction rate measurements obtained at intrinsic kinetic conditions, viz., without limitation of the reaction rate by mass transport, irrespective of the order of the reaction kinetics. For positive order kinetics, this is good practice and the kinetic rate parameters can be safely applied both at intrinsic and mass transport limited conditions. However, for negative order kinetics, erroneous results are obtained because the kinetic rate parameters estimated at intrinsic kinetic conditions fail to predict the reaction rate when mass transport limitation also plays a role. This is demonstrated for the simple case of Langmuir–Hinshelwood (LH) negative-order kinetics and for the, more complex, kinetics of the oxidation of methyl α -D-glucopyranoside on noble metal catalysts. It is concluded that for a negative-order reaction rate model, which is valid for a wide range of reaction conditions, the kinetic rate parameters need to be estimated both at intrinsic and mass transport limited conditions.

Full Text
Paper version not known

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.