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PdAgAu alloy films were prepared on porous stainless steel supports by sequential electroless deposition. Two specific compositions, Pd83Ag2Au15 and Pd74Ag14Au12, were studied for their sulfur tolerance. The alloys and a reference Pd foil were exposed to 1000H2S/H2 at 623 K for periods of 3 and 30 h. The microstructure, morphology and bulk composition of both non-exposed and H2S-exposed samples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM) and energy-dispersive X-ray spectroscopy (EDS). XRD and SEM analysis revealed time-dependent growth of a bulk Pd4S phase on the Pd foil during H2S exposure. In contrast, the PdAgAu ternary alloys displayed the same FCC structure before and after H2S exposure. In agreement with the XRD and SEM results, sulfur was not detected in the bulk of either ternary alloy samples by EDS, even after 30 h of H2S exposure. X-ray photoelectron spectroscopy (XPS) depth profiles were acquired for both PdAgAu alloys after 3 and 30 h of exposure to characterize sulfur contamination near their surfaces. Very low S 2p and S 2s XPS signals were observed at the top-surfaces of the PdAgAu alloys, and those signals disappeared before the etch depth reached ∼10 nm, even for samples exposed to H2S for 30 h. The depth profile analyses also revealed silver and gold segregation to the surface of the alloys; preferential location of Au on the alloys surface may be related to their resistance to bulk sulfide formation. In preliminary tests, a PdAgAu alloy membrane displayed higher initial H2 permeability than a similarly prepared pure Pd sample and, consistent with resistance to bulk sulfide formation, lower permeability loss in H2S than pure Pd. Fil: Braun, Fernando. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera". Universidad Nacional del Litoral. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera"; Argentina Fil: Miller, James. University of Carnegie Mellon; Estados Unidos Fil: Gellman, Andrew J. University of Carnegie Mellon; Estados Unidos Fil: Tarditi, Ana Maria. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera". Universidad Nacional del Litoral. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera"; Argentina Fil: Fleutot, Benoit. University of Carnegie Mellon; Estados Unidos Fil: Kondratyuk, Petro. University of Carnegie Mellon; Estados Unidos Fil: Cornaglia, Laura Maria. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera". Universidad Nacional del Litoral. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera"; Argentina

PdRu films were successfully synthesized on top of non-porous stainless steel supports by electroless co-deposition. The effect of synthesis variables on morphology, substrate adherence, bulk and surface composition was studied. The microstructure and morphology of the samples were analyzed by X-ray diffraction and scanning electron microscopy. Homogeneous and defect-free PdRu films were obtained employing baths at low pH, moderate to high agitation speeds, high concentration of hydrazine, using EDTA as a stabilizer and temperatures near 50°C. Films characterized by X-ray photoelectron spectroscopy showed Pd segregation after annealing the sample at 400°C in H2 (5%)/Ar in the load-lock chamber of the spectrometer. The optimized conditions were employed to synthesize a PdRu composite membrane on top of a tubular porous stainless steel substrate (0.1μm grade). Hydrogen permeation was measured over a 350-450°C temperature range and a trans-membrane pressure up to 100kPa. The PdRu membrane showed good performance with a hydrogen permeability of 6.5×10-9molm-1s-1Pa-0.5 and a selectivity higher than 1700. Fil: Braun, Fernando. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera". Universidad Nacional del Litoral. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera"; Argentina Fil: Tarditi, Ana Maria. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera". Universidad Nacional del Litoral. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera"; Argentina Fil: Cornaglia, Laura Maria. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera". Universidad Nacional del Litoral. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera"; Argentina

Dense PdAgCu ternary alloy composite membranes were synthesized by the sequential electroless plating of Pd, Ag and Cu on top of both disk and tubular porous stainless steel substrates. X-ray diffraction and scanning electron microscopy were employed to study the structure and morphology of the tested samples. The hydrogen permeation performance of these membranes was investigated over a 350–450 °C temperature range and a trans-membrane pressure up to 100 kPa. After annealing at 500 °C in hydrogen stream followed by permeation experiments, the alloy layer presented a FCC crystalline phase with a bulk concentration of 68% Pd, 7% Ag and 25% Cu as revealed by EDS. The PdAgCu tubular membrane was found to be stable during more than 300 h on hydrogen stream. The permeabilities of the PdAgCu ternary alloy samples were higher than the permeabilities of the PdCu alloy membranes with a FCC phase. The co-segregation of silver and copper to the membrane surface was observed after hydrogen permeation experiments at high temperature as determined by XPS.

PdCuAu ternary alloy membranes with different component compositions were synthesized by sequential electroless deposition of components onto porous stainless steel substrates. The ternary with the highest Au content, Pd 69 Cu 14 Au 17 , exhibited the highest hydrogen permeation flux, comparable to that of a Pd 91 Au 9 membrane. Upon exposure to 100ppm H 2 S/H 2 at 673 K for 24h, all PdCuAu membranes experienced flux reductions of ~55%, followed by recovery to ~80% of the initial hydrogen flux upon reintroduction of pure hydrogen at 400°C. Complete flux recovery after H 2 S exposure required hydrogen treatment at 500°C. X-ray diffraction (XRD) analysis of the H 2 S-exposed PdCuAu membranes revealed fcc alloy structure with no evidence of bulk sulfide formation. In agreement with the XRD results, sulfur was not detected in the bulk of H 2 S-exposed samples by energy dispersive spectroscopy (EDS). However, analysis of H 2 S-exposed PdCuAu alloys by X-ray photoelectron spectroscopy (XPS) depth profiling revealed low, but measureable, amounts of sulfur in the near-surface region, about 10nm in depth. The depth profiles of samples after hydrogen recovery treatment showed significantly reduced sulfur content. These results indicate that H 2 S exposure causes flux loss in PdCuAu alloys through a surface-poisoning mechanism, and that the surface sulfide can be removed-and flux recovered-by high temperature treatment in hydrogen. Fil: Tarditi, Ana Maria. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera". Universidad Nacional del Litoral. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera"; Argentina Fil: Imhoff, Carolina Guadalupe. Universidad Nacional del Litoral. Facultad de Ingeniería Química; Argentina Fil: Braun, Fernando. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera". Universidad Nacional del Litoral. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera"; Argentina Fil: Miller, James B.. University of Carnegie Mellon; Estados Unidos Fil: Gellman, Andrew J.. University of Carnegie Mellon; Estados Unidos Fil: Cornaglia, Laura Maria. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera". Universidad Nacional del Litoral. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera"; Argentina

The hydrogen transfer reduction of an α,β-unsaturated ketone, mesityl oxide, was studied on several single oxides in the gas-phase using 2-propanol as a hydrogen source. Selectivity is essentially determined by oxide electronegativity because the reaction proceeds via surface intermediates formed by coordination of 2-propanol and also of C{double bond, long}O and C{double bond, long}C groups of the reactant ketone on the Lewis acid sites provided by the metal cations. Oxides that combine weak Lewis acid cations and strongly basic oxygens such as MgO or Y2O3 yield allylic alcohols as the main reduction products of the gas-phase reaction. Adsorption experiments on MgO monitored by FTIR spectroscopy show that competitive 2-propanol and mesityl oxide adsorption on Mg2+ cations favors the hydrogen transfer process by a concerted Meerwein-Ponndorf-Verley mechanism whereas strong mesityl oxide adsorption causes simultaneous reduction of C{double bond, long}O and C{double bond, long}C bonds with formation of the saturated alcohol. High reaction temperatures strongly affect the stability of the complex reaction intermediates postulated for saturated and allylic alcohol formation, thereby favoring the simpler double bond migration reaction over the reduction reactions. More electronegative oxides such as ZrO2 or Al2O3 tend to promote the C{double bond, long}C bond reduction giving the saturated ketone. On these oxides, 2-propanol decomposes into acetone and molecular hydrogen at high rates, which is detrimental to carbonyl reduction. Fil: Braun, Fernando. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera". Universidad Nacional del Litoral. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera"; Argentina Fil: Di Cosimo, Juana Isabel. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera". Universidad Nacional del Litoral. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera"; Argentina

Pd, Pd90Ag10, Pd91Au9, Pd78Ag9Au13 and Pd75Ag16Au9 alloy membranes were prepared on vacuum-assisted ZrO2-modified porous stainless steel supports by sequential electroless deposition. The membranes were evaluated for permeability in pure H2 and in an H2S/H2 mixture. The membranes displayed a range of permeabilities in pure H2: Pd90Ag10>Pd78Ag9Au13>Pd~Pd75Ag16Au9>Pd91Au9. On exposure to 100 ppm H2S/H2 at 673 K for 24 h, all membranes lost a significant fraction of their H2 permeabilities: Pd (lost the largest fraction, 85%)>Pd90Ag10>Pd75Ag16Au9>Pd78Ag9Au13>Pd91Au9 (60%). When H2S was removed, the membranes recovered the lost permeability to different extents. The Pd91Au9 and Pd78Ag9Au13 membranes displayed the highest fractional recovery of initial H2 permeability (~80%). But, with its higher initial pure H2 permeability, Pd78Ag9Au13 had the highest absolute H2 permeability after recovery. The microstructure, morphology and bulk composition of H2S-exposed samples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM) and energy-dispersive X-ray spectroscopy (EDS). XRD revealed the presence of a bulk Pd4S phase on both Pd and Pd90Ag10, the membranes that recovered the least H2 relative flux after their exposure to H2S. In contrast, bulk sulfides did not form on Pd91Au9 or on PdAgAu ternary alloys. In agreement with the XRD results, EDS did not detect sulfur in the bulk of Pd91Au9 or in either of the ternary alloy samples. Our results show that the addition of Au to the high-permeability PdAg binary membrane results in a PdAgAu ternary membrane that minimizes the permanent H2 flux loss associated with H2S exposure by preventing the formation of thick stable sulfides. Fil: Braun, Fernando. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica ; Argentina Fil: Tarditi, Ana Maria. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica ; Argentina Fil: Miller, James B.. University of Carnegie Mellon. Department of Chemical Engineering; Estados Unidos. United States Department of Energy; Estados Unidos Fil: Cornaglia, Laura Maria. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica ; Argentina