Open Access
Multifunctional heterogeneous catalysts: Tetrakis (pentafluorophenyl)porphinato]iron(III) immobilized on amine-functionalized Diatomaceous Earth for catalytic and adsorption applications
(Elsevier, 2023) Do Prado, Marcus Vinicius; González, Beatriz; Vicente, Miguel Ángel; Trujillano, Raquel; Nassar, Eduardo José; Gil Bravo, Antonio; Santamaría Arana, Leticia; Korili, Sophia A.; Marçal, Liziane; Faria, Emerson H. de; Ciuffi, Katia J.; Ciencias; Zientziak; Institute for Advanced Materials and Mathematics - INAMAT2; Universidad Pública de Navarra / Nafarroako Unibertsitate Publikoa
The use of Diatomaceous Earth (DE) as a promising support of a synthetic metalloporphyrin is reported, trying to heterogenize metalloporphyrin catalysts to mimicking enzyme site isolation and improving reaction selectivity. New multifunctional hybrid materials consisting of DE amino–functionalized with aminopropyltriethoxysilane (DE–APTES), followed by grafting with [meso–tetrakis(pentafluorophenyl)porphinato]iron(III) (DE–APTES–FeTFPP), were prepared and fully characterized. FeTFPP was grafted into DE–APTES via the amine groups (band at 1570 cm–1 ). The brown color of the materials indicated that FeTFPP was immobilized in the matrix; a Soret band characteristic of ironporphyrin located in a confined space, was found at 416 nm. Leaching studies confirmed that the ironporphyrin was entrapped and not just adsorbed on the silica surface. DE was composed of typical quartz and cristobalite crystalline phases and amorphous silica. The intensity of its characteristic reflection at 22◦ (2θ) decreased in the presence of FeTFPP, evidencing that the ironporphyrin influenced the organization of the material. Catalytic tests using DE–APTES–FeTFPP in cyclooctene epoxidation to cyclooctene oxide (56 % yield, with complete selectivity for the epoxide) and cyclohexane oxidation (4 % yield of oxidized products, with ketone/alcohol selectivity ~ 3:1), evidenced the versatility of the catalyst and the multifunctionality of the resulting hybrid materials and the ability of DE as a promising natural support for ironporphyrin catalysts. Finally, the capacity of the materials as CO2 adsorbents was evaluated in the temperature range 100–200 ◦C. DE–APTES showed a maximum adsorption capacity of 1.26 mmol/g at 100 ◦C, 18 times higher than the value found under the same conditions for the non–functionalized support.
Open Access
Metal-Al layered double hydroxides synthesized from aluminum slags as efficient CO2 adsorbents at pre- and post-combustion temperature
(Elsevier, 2023) Santamaría Arana, Leticia; Korili, Sophia A.; Gil Bravo, Antonio; Ciencias; Zientziak; Institute for Advanced Materials and Mathematics - INAMAT2; Universidad Pública de Navarra / Nafarroako Unibertsitate Publikoa
Layered double hydroxides (LDH) have been proposed as the materials that offer the best performance in the moderate-temperature range, between 200 and 450 °C, for CO2 adsorption, so the effect of some synthesis parameters and surface modification on their adsorption capacities is herein investigated. This work reports the use of M2+ (Co, Mg, Ni and Zn)/Al layered double hydroxides synthesized with a 3:1 molar ratio by the co-precipitation method and using aluminum extracted from saline slags as source of this metal as CO2 adsorbents. The synthesis and use of Zn/TiAl is also reported considering several proportions of Al-Ti. Structural characterization and comparison of the series has been achieved using powder X-ray diffraction (PXRD), scanning electron microscopy (SEM), nitrogen physisorption at single bond196 °C and thermogravimetry measurements (TGA). The performance of calcined LDH as CO2 adsorbents was evaluated in the 50 – 400 °C temperature range and 80 kPa and results show that Ni6Al2 and Mg6Al2 samples present a significant adsorption capacity at low temperature (0.382 and 0.292 mmolCO2/g, respectively). At 400 °C only Mg6Al2 maintains its high adsorption capacity (0.275 mmolCO2/g) compared to the other calcined LDH. Its adsorption capacity at moderate-temperature range was proven to be better than that of a commercial Mg6Al2 sample. In all materials the CO2 adsorption capacity at 200–450 °C increased by incorporating potassium (K2CO3 and KOH as sources) up to 0.58 mmolCO2/g for Mg6Al2 +K2CO3. The addition of the amine TEPA in the low-temperature range worked for Co6Al2 and Mg6Al2 (increment > 40 %). In the case of Zn6Al2, the partial substitution of Al by Ti also increased the CO2 adsorption capacity from 0.177 to 0.244 mmolCO2/g, finding isosteric heats between 17.07 and 23.30 kJ/mol using the Clausius-Clapeyron equation.
Open Access
Layered double hydroxides for CO2 adsorption at moderate temperatures: synthesis and amelioration strategies
(Elsevier, 2023) Santamaría Arana, Leticia; Korili, Sophia A.; Gil Bravo, Antonio; Ciencias; Zientziak; Institute for Advanced Materials and Mathematics - INAMAT2; Universidad Pública de Navarra / Nafarroako Unibertsitate Publikoa
Curving the CO2 atmospheric levels is one of the challenges of this century, given its direct impact on climate change. Of the several strategies of CO2 capture and storage, sorption-enhanced water–gas shift (SEWGS) process, a combination of CO2 adsorption and the water–gas shift reaction, has been appointed as one of the most promising techniques due to is low energy consumption and high efficiency. SEWGS operating settings at both moderate temperature (200–450 ◦C) and high pressure (more than 10 bar) bring the need to find an adsorbent capable of working at these conditions. Calcined layered double hydroxides (LDH) have been proven to give the best results in this range of pressure/temperatures even though its performance can be greatly improved. Herein, a state-of-art of the research accomplished up until now is presented. Several strategies can be followed to improve the adsorbents performance: the synthesis method, LDH composition, modifications employed to promote their adsorption capacity or how the adsorption conditions can affect their efficiency

Korili, Sophia A.

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