To meet the stringent requirements of distributed hydrogen production, combined reaction-separation approaches to the endothermic steam methane reforming process have been investigated widely as a potential means to reduce the required reaction temperature, ratio of steam to methane in the fuel (or steam to carbon ratio), and number of sequential unit operation steps. The CHAMP-SORB is a new reactor technology for distributed hydrogen production from methane that incorporates both a hydrogen-selective membrane and CO 2 adsorption into a variable volume batch operation using a four stroke cycle. Active control of the reactor volume, and hence pressure, in combination with continuous removal of both reaction products allows CHAMP-SORB to circumnavigate the equilibrium limitations of the steam-methane reforming (SMR) reaction, which otherwise limit fuel conversion, especially at temperatures below 500°C with a stoichiometric fuel mixture. In this work, we present the first demonstration of an operating CHAMP-SORB reactor, achieving SMR at temperatures as low as 400°C and at a steam to carbon ratio of 2:1. A kinetic model of the CHAMP-SORB process is developed, verified for agreement with detailed experimental measurements, and used to investigate the interactions between the reaction, permeation, and adsorption processes. Timescale analysis is introduced to explore the relationship between reactor component design dcharacteristics and the ratelimiting steps of the CHAMP-SORB. Supported by the results of kinetic simulations, the scaling analysis provides a powerful tool for rapid exploration of the operating space, including operating temperatures and hydrogen collection/utilization pressures.