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Currently, the main limitations of Pd-coated Nb-TiFe dual-phase alloys include insufficient hydrogen permeability, susceptibility to hydrogen embrittlement (HE), and poor tolerance of H2S poisoning. To address these issues, this study proposes a series of improvements. First, a novel Nb15Ti55Fe30 alloy composed of a well-aligned Nb-TiFe eutectic was successfully prepared using directional solidification (DS) technology. After deposition with a Pd catalytic layer, this alloy exhibits high hydrogen permeability of 3.71 × 10−8 mol H2 m−1 s−1 Pa−1/2 at 673 K, which is 1.4 times greater than that of the as-cast counterpart. Second, to improve the H2S corrosion resistance, a new Pd88Au12 catalytic layer was deposited on the surface using a multi-target magnetic control sputtering system. Upon testing in a 100 ppm H2/H2S mixture, this membrane exhibited better resistance to bulk sulfidation and a higher permeance recovery (ca. 58%) compared to pure Pd-coated membrane. This improvement is primarily due to the lower adsorption energies of the former with H2S, which hinders the formation of bulk Pd4S. Finally, the composition region of the Pd-Au catalytic membrane with high comprehensive performance was determined for the first time, revealing that optimal performance occurs at around 12–18 at.% Au. This finding explains how this composition maintains a balance between high H2 permeability and excellent sulfur resistance. The significance of this study lies in its practical solutions for simultaneously improving hydrogen permeability and resistance to H2S poisoning in Nb-based composite membranes.
Currently, the main limitations of Pd-coated Nb-TiFe dual-phase alloys include insufficient hydrogen permeability, susceptibility to hydrogen embrittlement (HE), and poor tolerance of H2S poisoning. To address these issues, this study proposes a series of improvements. First, a novel Nb15Ti55Fe30 alloy composed of a well-aligned Nb-TiFe eutectic was successfully prepared using directional solidification (DS) technology. After deposition with a Pd catalytic layer, this alloy exhibits high hydrogen permeability of 3.71 × 10−8 mol H2 m−1 s−1 Pa−1/2 at 673 K, which is 1.4 times greater than that of the as-cast counterpart. Second, to improve the H2S corrosion resistance, a new Pd88Au12 catalytic layer was deposited on the surface using a multi-target magnetic control sputtering system. Upon testing in a 100 ppm H2/H2S mixture, this membrane exhibited better resistance to bulk sulfidation and a higher permeance recovery (ca. 58%) compared to pure Pd-coated membrane. This improvement is primarily due to the lower adsorption energies of the former with H2S, which hinders the formation of bulk Pd4S. Finally, the composition region of the Pd-Au catalytic membrane with high comprehensive performance was determined for the first time, revealing that optimal performance occurs at around 12–18 at.% Au. This finding explains how this composition maintains a balance between high H2 permeability and excellent sulfur resistance. The significance of this study lies in its practical solutions for simultaneously improving hydrogen permeability and resistance to H2S poisoning in Nb-based composite membranes.
The separation of high-purity hydrogen from mixed gasses using dense metallic alloy membranes is essential for advancing a hydrogen-based economy. Palladium-based membranes exhibit outstanding catalytic activity and theoretically infinite hydrogen selectivity, but their high cost and limited performance in contaminant-rich environments restrict their widespread use. This study addresses these limitations by exploring strategies to develop cost-effective, high-performance alternatives. Key challenges include the vast compositional design space, lack of systematic design principles, and the slow pace of traditional material development. This review emphasizes the potential of high-throughput and combinatorial techniques, such as composition-spread alloy films and the statistical design of experiments (DoE), combined with machine learning and materials informatics, to accelerate the discovery, optimization, and characterization of palladium-based membranes. These approaches reduce development time and costs while improving efficiency. Focusing on critical properties such as surface catalytic activity, resistance to chemical and physical stresses, and the incorporation of low-cost base metals, this study introduces domain-specific descriptors to address data scarcity and improve material screening. By integrating computational and experimental methods, future research can identify hidden material correlations and expedite the rational design of next-generation hydrogen separation membranes.
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