Open Access
Multifunctional nanocomposites based on kaolinite/titania/iron applied to hydrogen peroxide production and bisphenol-A removal
(Elsevier, 2024-11-06) Do Prado, Marcus Vinicius; Lima, Vinicius; Oliveira, Larissa; Nassar, Eduardo José; Marçal, Liziane; Faria, Emerson H. de; Vicente, Miguel Ángel; Trujillano, Raquel; Santamaría Arana, Leticia; Gil Bravo, Antonio; Korili, Sophia A.; Ciuffi, Katia J.; Ciencias; Zientziak; Institute for Advanced Materials and Mathematics - INAMAT2; Universidad Pública de Navarra / Nafarroako Unibertsitate Publikoa
The rising global demand for hydrogen peroxide, recognized for its eco-friendly properties, underscores the need for greener synthesis methods. Traditional production processes pose environmental risks, while direct synthesis faces challenges like water formation, explosion hazards, and stability issues, limiting industrial application. On the other hand, Bisphenol A (BPA), an endocrine disruptor widely used in plastics, presents significant environmental and health concerns due to its potential leaching into food and water. The present work introduces efficient and selective photocatalysts aimed at sustainable hydrogen peroxide synthesis and BPA degradation. Both processes were enhanced by the synergistic properties of Fe2O3–TiO2 nanoparticles dispersed within a kaolinite matrix. The Fe2O3-TiO2 photocatalysts, characterized by photoluminescence spectroscopy and X-ray diffraction, showed reduced emission upon iron incorporation and anatase presence on the kaolinite surface. The photocatalytic activity was evaluated through hydroxylation of terephthalic acid, revealing a 127 umol/L min hydroxylation rate for the KaFeTi400 sample. BPA degradation studies indicated optimal performance in acidic conditions, achieving 96 % removal in 2 h and 98 % in 4 h, with the addition of H2O2 enhancing efficiency. Further, the photocatalyst facilitated benzyl alcohol oxidation to benzaldehyde, demonstrating a H2O2 production rate of 120 umol. These findings highlight the multifunctional capabilities and environmental benefits of the photocatalyst, underscoring its potential for sustainable hydrogen peroxide synthesis and broader applications in environmental remediation. The catalysts address the pressing challenges associated with hydrogen peroxide synthesis and pollutant removal, particularly in the context of sustainability and environmental impact.
Open Access
Titania-triethanolamine-kaolinite nanocomposites as adsorbents and photocatalysts of herbicides
(Elsevier, 2021) Ferreira, Ana Vera de Toledo Piza Figueiredo; Barbosa, Lorrana Vietro; Souza, Suelen Delfino de; Ciuffi, Katia J.; Vicente, Miguel Ángel; Trujillano, Raquel; Korili, Sophia A.; Gil Bravo, Antonio; Faria, Emerson H. de; Zientziak; Institute for Advanced Materials and Mathematics - INAMAT2; Ciencias
Kaolinite-titania adsorbents/photocatalysts were prepared by functionalizing a kaolinite with titanium(IV) triethanolaminate isopropoxide by the sol–gel route. These materials were characterized by various techniques and applied in adsorption studies (kinetic and equilibrium) of the herbicides diuron, hexazinone, and tebuthiuron. Photodegradation studies were also conducted with the materials submitted to heat-treatment at 400, 700, or 1000 °C. The basal spacing increased from 0.71 to 1.08 nm when pure kaolinite was functionalized with titanium triethanolaminate units. The materials displayed FTIR bands of –CH, –NH2, and Ti–OH groups, thereby confirming that titanium alkoxide was present in the kaolinite interlayer space. The pseudo second-order model was the best for describing the kinetic adsorption process. In the equilibrium study, the Langmuir model best described the adsorption mechanism. The photodegradation studies showed that the kaolinite-titania nanocomposites heat-treated at 400 and 700 degraded diuron, hexazinone, and tebuthiuron efficiently due to the presence of metakaolin and formation of the anatase phase. © 2021 Elsevier B.V.
Open Access
White and red Brazilian Sao Simao's kaolinite-TiO2 nanocomposites as catalysts for toluene photodegradation from aqueous solutions
(MDPI, 2019) Mora, Lucas D.; Trujillano, Raquel; Rives, Vicente; Pérez Bernal, María Elena; Korili, Sophia A.; Gil Bravo, Antonio; Faria, Emerson H. de; Zientziak; Institute for Advanced Materials and Mathematics - INAMAT2; Ciencias
The presence of volatile organic compounds in groundwater is a major concern when it is used as a drinking water source because many of these compounds can adversely affect human health. This work reports on the preparation and characterization of white and red Brazilian Sao Simao's kaolinite-TiO2 nanocomposites and their use as catalysts in the photochemical degradation of toluene, a significant volatile organic compound. The nanocomposites were prepared by a sol-gel procedure, using titanium bis(triethanolaminate)diisopropoxide as a precursor. Thermal treatments of the nanocomposites led to different polymorphic titania phases, while the clay changed from kaolinite to metakaolinite. This structural evolution strongly affected the photocatalytic degradation behavior-all the solids efficiently degraded toluene and the solid calcined at 400 degrees C, formed by kaolinite and anatase, showed the best behavior (90% degradation). On extending the photochemical treatment up to 48 h, high mineralization levels were reached. The advantage of photodegradation using the nanocomposites was confirmed by comparing the results from isolated components (titanium dioxide and kaolinite) to observe that the nanocomposites displayed fundamental importance to the photodegradation pathways of toluene.
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
M(II)-Al-Fe layered double hydroxides synthesized from aluminum saline slag wastes and catalytic performance on cyclooctene oxidation
(Elsevier, 2022) Santamaría Arana, Leticia; Oliveira-Garcia, L.; Faria, Emerson H. de; Ciuffi, Katia J.; Vicente, Miguel Ángel; Korili, Sophia A.; Gil Bravo, Antonio; Institute for Advanced Materials and Mathematics - INAMAT2; Universidad Pública de Navarra / Nafarroako Unibertsitate Publikoa
Aluminum was extracted from saline slags via an alkaline method and employed in the synthesis of Layered Double Hydroxides (LDH) with various M2+ cations (Co, Mg, Ni and Zn), while Al and Fe were the M3+ cations, using the co-precipitation method and a M2+/M3+ 2:1 ratio. The structural characterization of the samples was performed with powder X-ray diffraction (PXRD), scanning electron microscopy (SEM), nitrogen physisorption at 77 K, thermogravimetric analysis (TGA), temperature-programmed reduction (TPR) and X-ray photoelectron spectroscopy (XPS). Their catalytic performance was tested for the oxidation of olefins (cyclooctene) and their biomimetic potential was analyzed. Results show a great selectivity towards epoxides with no other products obtained. Reaction yields followed the descending order Co4AlFe, Zn4AlFe, Ni4AlFe, and Mg4AlFe, the sample with cobalt as M2+ converting up to 85% of cyclooctene.
Open Access
Inorganic–organic hybrids based on sepiolite as efficient adsorbents of caffeine and glyphosate pollutants
(Elsevier, 2020) Baldan Junior, Hugo; Silva Grazziano, Eliane da; Saltarelli, Michelle; Crispim, Denise; Nassar, Eduardo José; Trujillano, Raquel; Rives, Vicente; Vicente, Miguel Ángel; Gil Bravo, Antonio; Korili, Sophia A.; Faria, Emerson H. de; Ciuffi, Katia J.; Institute for Advanced Materials and Mathematics - INAMAT2
Sepiolite clay mineral was functionalized with (3-chloropropyl)triethoxysilane (ClPTES) or 3-[tri(ethoxy/methoxy)silyl] propylurea (TEMSPU) alkoxides and tested as adsorbent for herbicide glyphosate and also of caffeine, two pollutants with very different chemical composition. The materials obtained were characterized by X-ray diffractometry, infrared spectroscopy, thermal analysis, scanning electron microscopy and nitrogen adsorption at −196 °C, and submitted to toxicity and desorption tests. Silane functional groups blocked sepiolite active positions, and adsorption occurred within the zeolitic channels and on the surface of the functionalized solids. Caffeine and glyphosate effectively interacted with urea groups from grafted alkoxide, which could lower the mobility of the adsorbed contaminants. Glyphosate adsorbed on functionalized sepiolite derivatives showed low toxicity.