4.5 Article

Versatile and Resistant Electroless Pore-Plated Pd-Membranes for H2-Separation: Morphology and Performance of Internal Layers in PSS Tubes

期刊

MEMBRANES
卷 12, 期 5, 页码 -

出版社

MDPI
DOI: 10.3390/membranes12050530

关键词

palladium; electroless plating; composite membrane; intermediate layer; PSS; internal surface; hydrogen; concentration-polarization; CO inhibition

资金

  1. Spanish State Research Agency (Agencia Estatal de Investigacion, AEI) through the competitive projects [ENE2017-83696-R, PID2020-117273RB-I00]
  2. Community of Madrid
  3. Rey Juan Carlos University [M2182-MEMRESPIP]

向作者/读者索取更多资源

This study explores the incorporation of CeO2 and Pd films onto the internal side of PSS tubes for additional protection. The prepared membranes demonstrate excellent mechanical resistance and similar performance to those prepared on the external surface. The membranes exhibit good conformity to Sieverts' law, with high H-2 permeance and complete ideal perm-selectivity. The permeate fluxes decrease with dilution and temperature in H-2 mixtures, and the presence of CO further inhibits the flux, but it can be completely recovered by feeding pure hydrogen again.
Pd-membranes are interesting in multiple ultra-pure hydrogen production processes, although they can suffer inhibition by certain species or abrasion under fluidization conditions in membrane reactors, thus requiring additional protective layers to ensure long and stable operation. The ability to incorporate intermediate and palladium films with enough adherence on both external and internal surfaces of tubular porous supports becomes crucial to minimize their complexity and cost. This study addresses the incorporation of CeO2 and Pd films onto the internal side of PSS tubes for applications in which further protection could be required. The membranes so prepared, with a Pd-thickness around 12-15 mu m, show an excellent mechanical resistance and similar performance to those prepared on the external surface. A good fit to Sieverts' law with an H-2-permeance of 4.571 x 10(-3) mol m(-2) s(-1) Pa-0.5 at 400 degrees C, activation energy around 15.031 kJ mol(-1), and complete ideal perm-selectivity was observed. The permeate fluxes reached in H-2 mixtures with N-2, He, or CO2 decreased with dilution and temperature due to the inherent concentration-polarization. The presence of CO in mixtures provoked a higher decrease because of a further inhibition effect. However, the original flux was completely recovered after feeding again with pure hydrogen, maintaining stable operation for at least 1000 h.

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