Nanomaterials in Catalysis: Design, Characterization and Applications

A special issue of Catalysts (ISSN 2073-4344). This special issue belongs to the section "Nanostructured Catalysts".

Deadline for manuscript submissions: closed (31 January 2024) | Viewed by 2936

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Centro de Química Estrutural, Instituto Superior Técnico, Universidade de Lisboa, Av. Rovisco Pais, 1049-001 Lisboa, Portugal
Interests: catalysis; nanomaterials; green metrics; sustainability; mechanochemistry; biomass
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Special Issue Information

Dear Colleagues,

As catalysis is one of the key technologies for sustainable energy and the environment, the past few years have seen increasing numbers of nanomaterials being reported for these applications. Depending on the application, a number of different catalyst synthesis, characterization, and optimization protocols can be used. This Special Issue, entitled “Nanomaterials in Catalysis: Design, Characterization and Applications“, aims to highlight and present the current and future impacts of the emerging development and synthesis of a diverse range of nanomaterials in catalysis.

This Special Issue considers all aspects related to the use of nanomaterials for environmental science and engineering, including the synthesis, characterization, and utilization of nanomaterials for water/air/solid purification and energy production and storage.

Dr. Ana Paula da Costa Ribeiro
Guest Editor

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Keywords

  • catalysts
  • nanomaterials
  • nanoparticles
  • synthesis of nanomaterials
  • characterization of nanomaterials
  • environment protection
  • environment remediation
  • energy production
  • energy storage

Published Papers (3 papers)

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Research

20 pages, 7989 KiB  
Article
Au Nanoparticles Supported on Hydrotalcite-Based MMgAlOx (M=Cu, Ni, and Co) Composite: Influence of Dopants on the Catalytic Activity for Semi-Hydrogenation of C2H2
by Xun Sun, Wenrui Lv, Yanan Cheng, Huijuan Su, Libo Sun, Lijun Zhao, Zifan Wang and Caixia Qi
Catalysts 2024, 14(5), 315; https://doi.org/10.3390/catal14050315 - 10 May 2024
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Abstract
Semi-hydrogenation of acetylene to ethylene over metal oxide-supported Au nanoparticles is an interesting topic. Here, a hydrotalcite-based MMgAlOx (M=Cu, Ni, and Co) composite oxide was exploited by introducing different Cu, Ni, and Co dopants with unique properties, and then used as support [...] Read more.
Semi-hydrogenation of acetylene to ethylene over metal oxide-supported Au nanoparticles is an interesting topic. Here, a hydrotalcite-based MMgAlOx (M=Cu, Ni, and Co) composite oxide was exploited by introducing different Cu, Ni, and Co dopants with unique properties, and then used as support to obtain Au/MMgAlOx catalysts via a modified deposition–precipitation method. XRD, BET, ICP-OES, TEM, Raman, XPS, and TPD were employed to investigate their physic-chemical properties and catalytic performances for the semi-hydrogenation of acetylene to ethylene. Generally, the catalytic activity of the Cu-modified Au/CuMgAlOx catalyst was higher than that of the other modified catalysts. The TOR for Au/CuMgAlOx was 0.0598 h−1, which was 30 times higher than that of Au/MgAl2O4. The SEM and XRD results showed no significant difference in structure or morphology after introducing the dopants. These dopants had an unfavorable effect on the Au particle size, as confirmed by the TEM studies. Accordingly, the effects on catalytic performance of the M dopant of the obtained Au/MMgAlOx catalyst were improved. Results of Raman, NH3-TPD, and CO2-TPD confirmed that the Au/CuMgAlOx catalyst had more basic sites, which is beneficial for less coking on the catalyst surface after the reaction. XPS analysis showed that gold nanoparticles exhibited a partially oxidized state at the edges and surfaces of CuMgAlOx. Besides an increased proportion of basic sites on Au/CuMgAlOx catalysts, the charge transfer from nanogold to the Cu-doped matrix support probably played a positive role in the selective hydrogenation of acetylene. The stability and deactivation of Au/CuMgAlOx catalysts were also discussed and a possible reaction mechanism was proposed. Full article
(This article belongs to the Special Issue Nanomaterials in Catalysis: Design, Characterization and Applications)
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17 pages, 9298 KiB  
Article
TiO2/Zeolite Composites for SMX Degradation under UV Irradiation
by Saule Mergenbayeva, Zhanibek Abitayev, Milana Batyrbayeva, John Vakros, Dionissios Mantzavinos, Timur Sh. Atabaev and Stavros G. Poulopoulos
Catalysts 2024, 14(2), 147; https://doi.org/10.3390/catal14020147 - 16 Feb 2024
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Abstract
Sulfamethoxazole (SMX) is a common antibiotic that is considered an emerging pollutant of water bodies, as it is toxic for various aquatic species. TiO2-based photocatalysis is a promising method for SMX degradation in water. In this work, TiO2/zeolite (Z-45 [...] Read more.
Sulfamethoxazole (SMX) is a common antibiotic that is considered an emerging pollutant of water bodies, as it is toxic for various aquatic species. TiO2-based photocatalysis is a promising method for SMX degradation in water. In this work, TiO2/zeolite (Z-45 loaded with TiO2 labeled as TZ and ZSM-5 loaded with TiO2 labeled as TZSM) composites were prepared by mechanical mixing and liquid impregnation methods, and the photocatalytic performance of these composites (200 mg·L−1) was investigated toward the degradation of SMX (30 mg·L−1) in water under UV light (365 nm). The pseudo-first-order reaction rate constant of the TZSM1450 composite was 0.501 min−1, which was 2.08 times higher than that of TiO2 (k = 0.241 min−1). Complete SMX degradation was observed in 10 min using the UV/TZSM1450 system. The mineralization ability in terms of total organic carbon (TOC) removal was also assessed for all of the prepared composites. The results showed that 65% and 67% of SMX could be mineralized within 120 min of photocatalytic reaction by TZSM2600 and TZSM1450, respectively. The presence of Cl and CO32 anions inhibited the degradation of SMX, while the presence of NO3 had almost no effect on the degradation efficiency of the UV/TZSM1450 system. The electrical energy per order estimated for the prepared composites was in the range of 68.53–946.48 kWh m−3 order−1. The results obtained revealed that the TZSM1450 composite shows promising potential as a photocatalyst for both the degradation and mineralization of SMX. Full article
(This article belongs to the Special Issue Nanomaterials in Catalysis: Design, Characterization and Applications)
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16 pages, 3611 KiB  
Article
Characterization and Catalytic Performance of Al-SBA-15 Catalyst Fabricated Using Ionic Liquids with High Aluminum Content
by Obaid F. Aldosari, Mosaed S. Alhumaimess, Mohamed A. Betiha, Emad A. Ahmed, Laila M. Alhaidari, Afnan Altwala and Hassan M. A. Hassan
Catalysts 2023, 13(11), 1395; https://doi.org/10.3390/catal13111395 - 26 Oct 2023
Viewed by 1056
Abstract
This study involved the fabrication of a set of aluminum ion-grafted SBA-15 utilizing ethylenediamine and trimethylamine ionic liquids. The primary objective was to examine the impact of the fabrication environment on the physicochemical characteristics of the catalysts. Comprehensive characterization of the Al-SBA-15 catalysts [...] Read more.
This study involved the fabrication of a set of aluminum ion-grafted SBA-15 utilizing ethylenediamine and trimethylamine ionic liquids. The primary objective was to examine the impact of the fabrication environment on the physicochemical characteristics of the catalysts. Comprehensive characterization of the Al-SBA-15 catalysts was conducted using various techniques, including XRD, FTIR, surface area, pyridine FTIR, 27Al-NMR, TGA, HRTEM, and FESEM, to analyze their physicochemical characteristics. Furthermore, the acidic characteristics were examined by conducting potentiometric titration in a nonaqueous solvent and employing FTIR spectroscopy to analyze the chemisorbed pyridine. The effectiveness of the fabricated acid materials was evaluated by testing their performance in acetic acid esterification with butanol. The findings obtained reveal that mesostructured SBA-15 remains intact following the successful inclusion of Al3+ ions into the silica frameworks. Additionally, a remarkable enhancement in the existence of both Bronsted and Lewis acid centers was noted due to the grafting process of Al3+ ions. At temperatures of 80 °C and 100 °C, the reaction in Al-SBA-15(T-120) proceeds swiftly, reaching approximately 32% and 38% conversion, respectively, within a span of 110 min. The excellent catalytic performance observed in the esterification reaction can be attributed to two factors: the homogeneous distribution of Al3+ ions within the SBA-15 frameworks and the acidic character of Al-SBA-15. The findings further indicate that the grafting process for incorporating Al3+ ions into the silica matrix is more efficient. Full article
(This article belongs to the Special Issue Nanomaterials in Catalysis: Design, Characterization and Applications)
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