David Curran
David Curran
*This is an algorithmically generated author record based on publicly available information.
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Research Interests
David Curran has a total of 6 co-authors. Here are the top co-authors by number of shared publications:
- Benjamin L. Kee
Department of Mechanical Engineering, Colorado School of Mines, 1500 Illinois Street, Golden, CO 80401, USA
1 shared publication - Huayang Zhu
Engineering Division, Colorado School of Mines, Golden, Colorado 80401, USA
1 shared publication - Robert J. Braun
Department of Mechanical Engineering, Colorado School of Mines, Golden, Colorado 80401, United States of America
1 shared publication - Robert J. Kee
Colorado School of Mines
1 shared publication - Sandrine Ricote
Colorado School of Mines
1 shared publication - Steven C. DeCaluwe
Colorado School of Mines
1 shared publication
Latest Publications
- Open Access
Thermodynamic Insights for Electrochemical Hydrogen Compression with Proton-Conducting Membranes
Membrane electrode assemblies (MEA) based on proton-conducting electrolyte membranes offer opportunities for the electrochemical compression of hydrogen. Mechanical hydrogen compression, which is more-mature technology, can suffer from low reliability, noise, and maintenance costs. Proton-conducting electrolyte membranes may be polymers (e.g., Nafion) or protonic-ceramics (e.g., yttrium-doped barium zirconates). Using a thermodynamics-based analysis, the paper explores technology implications for these two membrane types. The operating temperature has a dominant influence on the technology, with polymers needing low-temperature and protonic-ceramics needing elevated temperatures. Polymer membranes usually require pure hydrogen feed streams, but can compress H efficiently. Reactors based on protonic-ceramics can effectively integrate steam reforming, hydrogen separation, and electrochemical compression. However, because of the high temperature (e.g., 600 C) needed to enable viable proton conductivity, the efficiency of protonic-ceramic compression is significantly lower than that of polymer-membrane compression. The thermodynamics analysis suggests significant benefits associated with systems that combine protonic-ceramic reactors to reform fuels and deliver lightly compressed H (e.g., 5 bar) to an electrochemical compressor using a polymer electrolyte to compress to very high pressure.Open AccessThermodynamic Insights for Electrochemical Hydrogen Compression with Proton-Conducting Membranes
Membrane electrode assemblies (MEA) based on proton-conducting electrolyte membranes offer opportunities for the electrochemical compression of hydrogen. Mechanical hydrogen compression, which is more-mature technology, can suffer from low reliability, noise, and maintenance costs. Proton-conducting electrolyte membranes may be polymers (e.g., Nafion) or protonic-ceramics (e.g., yttrium-doped barium zirconates). Using a thermodynamics-based analysis, the paper explores technology implications for these two membrane types. The operating temperature has a dominant influence on the technology, with polymers needing low-temperature and protonic-ceramics needing elevated temperatures. Polymer membranes usually require pure hydrogen feed streams, but can compress H efficiently. Reactors based on protonic-ceramics can effectively integrate steam reforming, hydrogen separation, and electrochemical compression. However, because of the high temperature (e.g., 600 C) needed to enable viable proton conductivity, the efficiency of protonic-ceramic compression is significantly lower than that of polymer-membrane compression. The thermodynamics analysis suggests significant benefits associated with systems that combine protonic-ceramic reactors to reform fuels and deliver lightly compressed H (e.g., 5 bar) to an electrochemical compressor using a polymer electrolyte to compress to very high pressure.