NaA zeolite membranes on modified porous stainless steel supports: A comparative study of different SiO2 sources

The deposition of a NaA zeolite layer on porous stainless steel substrates was optimized in order to obtain composite membranes for hydrogen separation. The effect of the silica source on NaA zeolite crystallinity and morphology was studied using two synthesis routes: concentrated gel and clear solution. The optimized synthesis conditions were applied for the synthesis of NaA zeolitelayers on top of porous stainless steel disks or on the outer surface of tubular supports. SEM and XRD measurements confirmed that the use of rice husk allowed obtaining defect free and pure phase NaA zeolite membrane. Selectivity values similar to those published for NaA zeolite membranes based in ceramic substrates were obtained using zeolite layers deposited on porous stainless steel tubes. From the curve fitting of the experimental data, the contribution of zeoliticand non-zeolitic flux was estimated. For the membranes synthesized from a concentrated gel, H2 showed a predominated contribution of the zeolitic flux.Fil: Martinez Galeano, Yohana. 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"; ArgentinaFil: 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"; ArgentinaFil: 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"; Argentin

NaA zeolite membranes synthesized on top of APTES-modified porous stainless steel substrates

NaA zeolite membranes were synthesized on top of both disk and tubular porous stainless steel substrates by the secondary growth method. The support seed stage was optimized, considering the seed synthesis conditions and the deposition method. The formation of the NaA zeolite on both the membrane and the residual powder collected at the bottom of the vessel after synthesis was corroborated by X-ray diffraction (XRD). Scanning electron microscopy (SEM) revealed the formation of a film with well-defined crystals with a cubic morphology characteristic of the NaA zeolite. The support modification with 3-aminopropyltriethoxysilane improved the morphology and stability of the NaA zeolite membranes synthesized on top of porous stainless steel substrates. When vacuum was applied only in the last hydrothermal synthesis stage, a smooth zeolite layer was obtained on top of porous stainless steel supports. The single gas (H2, N2, CO2 and CH4) and mixture (H2/N2 and H2/CH4) perm-selective properties of the tubular membranes were evaluated as a function of temperature and pressure. Separation factors higher than the Knudsen coefficient were obtained in all membranes. The single gas H2 and CO2 permeation flux of the membranes increased with temperature indicating a preponderance of the activated diffusion over the Knudsen diffusion. The higher H2/CO2 ideal separation factors were 7.6 and 5.6 for the more selective tubular membranes, at 453 K and 100 kPa.Fil: Martinez Galeano, Yohana. 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"; ArgentinaFil: 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"; ArgentinaFil: 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"; Argentin

Synthesis of Pt-zeolite coated palladium alloys as catalytic membranes for hydrogen production

PdAu composite membranes were applied for the preparation of PtNaA-PdAu catalytic membranes for hydrogen production from the water gas shift reaction. In the first stage, the deposition of NaA zeolite on top of the PdAu alloys was optimized. Functionalization employing a 1.0 v/v % 3-aminopropyltriethoxysilane solution prior to both seeding and hydrothermal synthesis allowed obtaining a homogeneous and complete PdAu alloy surface coverage. Even though the NaA zeolite coverage decreased the pure hydrogen permeance at 623 K and 50 kPa in comparison with a PdAu membrane, the resistance to a CO containing stream was higher. From direct incorporation of Pt during the zeolite synthesis, a homogeneous, well-intergrown PtNaA zeolite coverage on top of a PdAu alloy membrane was obtained. PtNaA catalytic tubular membranes were evaluated in the water gas shift reaction at 673 K. The membranes were active and stable under reaction conditions, without evidence of methane formation.Fil: Dalla Fontana, Agustina. 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"; ArgentinaFil: Martinez Galeano, Yohana. 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"; ArgentinaFil: 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"; ArgentinaFil: 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"; Argentin

Pt encapsulated into NaA zeolite as catalyst for the WGS reaction

Pt catalysts were prepared by encapsulating the active metal in the NaA zeolite structure. The catalysts were prepared by hydrothermal synthesis using two heating sources, conventional heating through a thermal bath and microwave radiation. The synthesis time was significantly reduced using microwave radiation without affecting the crystallinity or metallic content of the solids obtained. By X-ray diffraction the presence of the pure NaA zeolite phase was confirmed in all the samples. XRD, XPS and TEM results suggested the presence of Pt particles preferentially located inside the crystalline structure. Pt_NaA catalysts were active and selective for the water gas shift reaction at 673 K. No methane formation was detected in any of the samples under the reaction conditions studied. The Pt_NaA catalyst with low Pt content (0.6% wt.) achieved a high conversion of CO (ca. 70%).Fil: Martinez Galeano, Yohana. 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"; ArgentinaFil: Negri, Florencia. 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"; ArgentinaFil: Moreno, Mario Sergio Jesus. Comisión Nacional de Energía Atómica. Centro Atómico Bariloche; ArgentinaFil: Múnera Agudelo, John 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"; ArgentinaFil: 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"; ArgentinaFil: 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"; Argentin