Special Issue "Photocatalysts for Organics Degradation"

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

Deadline for manuscript submissions: closed (31 July 2018)

Special Issue Editors

Guest Editor
Prof. Barbara Bonelli

Institute of Chemistry, Department of Applied Science and Technology; PoliTO BiomED Interdepartmental Lab; Politecnico di Torino, 10129 Torino, Italy
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Interests: nanoporous materials; heterogeneous catalysis; photocatalysis; gas adsorption and storage; emerging contaminants; dyes degradation; advanced oxidation processes; CO2 reduction; H2 production; spectroscopy; physical-chemistry
Guest Editor
Dr. Maela Manzoli

Department of Drug Science and Technology, Università degli Studi di Torino, Via Pietro Giuria 9, 10125 Torino, Italy
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Interests: Morphological and spectroscopic characterization of heterogeneous catalysts
Guest Editor
Dr. Francesca S. Freyria

Department of Chemistry, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, United States
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Interests: synthesis and characterization of heterostructured nanocrystals
Guest Editor
Dr. Serena Esposito

Department of Civil and Mechanical Engineering, Università degli Studi di Cassino e del Lazio Meridionale, Cassino (FR), Italy
Website | E-Mail
Interests: sol-gel synthesis; porous inorganic materials; surface properties; heterogeneous catalysis

Special Issue Information

Dear Colleagues,

This Issue is devoted to papers concerning the synthesis, the physico-chemical properties and the performance of photo-catalysts for the degradation of organic pollutants. Research papers, reviews and perspectives dealing with the photo-catalytic degradation of most common organic pollutants (dyes, pesticides, herbicides, etc.) are welcome, as well as papers dealing with the removal of emerging ones, like drugs and their metabolites. Authors are encouraged to enlighten several aspects, including the synthesis of novel photocatalysts (hybrid materials, quantum dots, colloidal nanoparticles, doped mesostructured materials, etc..), the optimization of processes utilizing state-of-art photocatalysts and the influence of the physico-chemical properties of the photocatalyst on its final performance. Since one of the main issues related to the photocatalytic degradation of organic pollutants is their actual mineralization as well as the formation of by-products that can be per se harmful, a number of papers dealing with the correct determination of mineralization as with the detection of such by-products is expected.

Prof. Dr. Barbara Bonelli
Dr. Maela Manzoli
Dr. Francesca S. Freyria
Dr. Serena Esposito
Guest Editors

Manuscript Submission Information

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Keywords

  • Novel synthesis of photocatalysts
  • Water remediation
  • Organic pollutants degradation
  • Harmful by-products
  • Advanced Oxidation processes
  • Physico-chemical properties of photocatalysts
  • Fenton, Fenton-like and photo-Fenton processes
  • Scale-up of photocatalytic processes
  • Detection of degradation products
  • Mineralization/Decoloration

Published Papers (5 papers)

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Research

Open AccessArticle Photocatalytic Behavior of Strontium Aluminates Co-Doped with Europium and Dysprosium Synthesized by Hydrothermal Reaction in Degradation of Methylene Blue
Catalysts 2018, 8(6), 227; https://doi.org/10.3390/catal8060227
Received: 4 April 2018 / Revised: 22 May 2018 / Accepted: 22 May 2018 / Published: 28 May 2018
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Abstract
Strontium aluminates co-doped with europium and dysprosium were prepared by a hydrothermal reaction through a sintering process at lower temperatures. The physicochemical properties of the strontium aluminates co-doped with europium and dysprosium were characterized and compared with those of strontium aluminates prepared by
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Strontium aluminates co-doped with europium and dysprosium were prepared by a hydrothermal reaction through a sintering process at lower temperatures. The physicochemical properties of the strontium aluminates co-doped with europium and dysprosium were characterized and compared with those of strontium aluminates prepared by a sol–gel method. The photocatalytic properties of the strontium aluminates co-doped with europium and dysprosium were evaluated through the photocatalytic decomposition of methylene blue dye. The strontium aluminates co-doped with europium and dysprosium prepared by the hydrothermal reaction exhibited good phosphorescence and photocatalytic activities that were similar to those prepared by the sol–gel method. The photocatalytic activity of these catalysts for methylene blue degradation was higher than that of the titanium dioxide (TiO2) photocatalyst. Full article
(This article belongs to the Special Issue Photocatalysts for Organics Degradation)
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Open AccessArticle Fabrication of a Z-Scheme g-C3N4/Fe-TiO2 Photocatalytic Composite with Enhanced Photocatalytic Activity under Visible Light Irradiation
Catalysts 2018, 8(3), 112; https://doi.org/10.3390/catal8030112
Received: 30 January 2018 / Revised: 7 March 2018 / Accepted: 8 March 2018 / Published: 13 March 2018
Cited by 4 | PDF Full-text (9094 KB) | HTML Full-text | XML Full-text
Abstract
In the present study, a nanocomposite material g-C3N4/Fe-TiO2 has been prepared successfully by a simple one-step hydrothermal process and its structural properties were thoroughly studied by various characterization techniques, such as X-ray diffraction (XRD), Fourier Transform Infrared (FTIR)
[...] Read more.
In the present study, a nanocomposite material g-C3N4/Fe-TiO2 has been prepared successfully by a simple one-step hydrothermal process and its structural properties were thoroughly studied by various characterization techniques, such as X-ray diffraction (XRD), Fourier Transform Infrared (FTIR) spectroscopy, electron paramagnetic resonance (EPR) spectrum, X-ray photoelectron spectroscopy (XPS), and UV-vis diffuse reflectance spectrometry (UV-vis DRS). The performance of the fabricated composite material towards the removal of phenol from aqueous phase was systematically evaluated by a photocatalytic approach and found to be highly dependent on the content of Fe3+. The optimum concentration of Fe3+ doping that showed a dramatic enhancement in the photocatalytic activity of the composite under visible light irradiation was observed to be 0.05% by weight. The separation mechanism of photogenerated electrons and holes of the g-C3N4/Fe-TiO2 photocatalysts was established by a photoluminescence technique in which the reactive species generated during the photocatalytic treatment process was quantified. The enhanced photocatalytic performance observed for g-C3N4-Fe/TiO2 was ascribed to a cumulative impact of both g-C3N4 and Fe that extended its spectrum-absorptive nature into the visible region. The heterojunction formation in the fabricated photocatalysts not only facilitated the separation of the photogenerated charge carriers but also retained its strong oxidation and reduction ability. Full article
(This article belongs to the Special Issue Photocatalysts for Organics Degradation)
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Open AccessArticle Highly Efficient and Visible Light Responsive Heterojunction Composites as Dual Photoelectrodes for Photocatalytic Fuel Cell
Catalysts 2018, 8(1), 30; https://doi.org/10.3390/catal8010030
Received: 11 November 2017 / Revised: 18 December 2017 / Accepted: 8 January 2018 / Published: 18 January 2018
Cited by 1 | PDF Full-text (4013 KB) | HTML Full-text | XML Full-text
Abstract
In the present work, a novel photocatalytic fuel cell (PFC) system involving a dual heterojunction photoelectrodes, viz. polyaniline/TiO2 nanotubes (PANI/TiO2 NTs) photoanode and CuO/Co3O4 nanorods (CuO/Co3O4 NRs) photocathode, has been designed. Compared to TiO2
[...] Read more.
In the present work, a novel photocatalytic fuel cell (PFC) system involving a dual heterojunction photoelectrodes, viz. polyaniline/TiO2 nanotubes (PANI/TiO2 NTs) photoanode and CuO/Co3O4 nanorods (CuO/Co3O4 NRs) photocathode, has been designed. Compared to TiO2 NTs electrode of PFC, the present heterojunction design not only enhances the visible light absorption but also offers the higher efficiency in degrading Rhodamine B–a model organic pollutant. The study includes an evaluation of the dual performance of the photoelectrodes as well. Under visible-light irradiation of 3 mW cm−2, the cell composed of the photoanode PANI/TiO2 NTs and CuO/Co3O4 NRs photocathode forms an interior bias of +0.24 V within the PFC system. This interior bias facilitated the transfer of electrons from the photoanode to photocathode across the external circuit and combined with the holes generated therein along with a simultaneous power production. In this manner, the separation of electron/hole pair was achieved in the photoelectrodes by releasing the holes and electrons of PANI/TiO2 NTs photoanode and CuO/Co3O4 NRs photocathode, respectively. Using this PFC system, the degradation of Rhodamine B in aqueous media was achieved to an extent of 68.5% within a reaction duration of a four-hour period besides a simultaneous power generation of 85 μA cm−2. Full article
(This article belongs to the Special Issue Photocatalysts for Organics Degradation)
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Open AccessArticle Low-Temperature Sol-Gel Synthesis of Nitrogen-Doped Anatase/Brookite Biphasic Nanoparticles with High Surface Area and Visible-Light Performance
Catalysts 2017, 7(12), 376; https://doi.org/10.3390/catal7120376
Received: 21 October 2017 / Revised: 26 November 2017 / Accepted: 30 November 2017 / Published: 4 December 2017
Cited by 1 | PDF Full-text (2832 KB) | HTML Full-text | XML Full-text | Supplementary Files
Abstract
Nitrogen doping in combination with the brookite phase or a mixture of TiO2 polymorphs nanomaterials can enhance photocatalytic activity under visible light. Generally, nitrogen-dopedanatase/brookite mixed phases TiO2 nanoparticles obtained by hydrothermal or solvothermal method need to be at high temperature and
[...] Read more.
Nitrogen doping in combination with the brookite phase or a mixture of TiO2 polymorphs nanomaterials can enhance photocatalytic activity under visible light. Generally, nitrogen-dopedanatase/brookite mixed phases TiO2 nanoparticles obtained by hydrothermal or solvothermal method need to be at high temperature and with long time heating treatment. Furthermore, the surface areas of them are low (<125 m2/g). There is hardly a report on the simple and direct preparation of N-doped anatase/brookite mixed phase TiO2 nanostructures using sol-gel method at low heating temperature. In this paper, the nitrogen-doped anatase/brookite biphasic nanoparticles with large surface area (240 m2/g) were successfully prepared using sol-gel method at low temperature (165 °C), and with short heating time (4 h) under autogenous pressure. The obtained sample without subsequent annealing at elevated temperatures showed enhanced photocatalytic efficiency for the degradation of methyl orange (MO) with 4.2-, 9.6-, and 7.5-fold visible light activities compared to P25 and the amorphous samples heated in muffle furnace with air or in tube furnace with a flow of nitrogen at 165 °C, respectively. This result was attributed to the synergistic effects of nitrogen doping, mixed crystalline phases, and high surface area. Full article
(This article belongs to the Special Issue Photocatalysts for Organics Degradation)
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Open AccessArticle Saturated Resin Ectopic Regeneration by Non-Thermal Dielectric Barrier Discharge Plasma
Catalysts 2017, 7(12), 362; https://doi.org/10.3390/catal7120362
Received: 26 October 2017 / Revised: 21 November 2017 / Accepted: 22 November 2017 / Published: 27 November 2017
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Abstract
Textile dyes are some of the most refractory organic compounds in the environment due to their complex and various structure. An integrated resin adsorption/Dielectric Barrier Discharge (DBD) plasma regeneration was proposed to treat the indigo carmine solution. It is the first time to
[...] Read more.
Textile dyes are some of the most refractory organic compounds in the environment due to their complex and various structure. An integrated resin adsorption/Dielectric Barrier Discharge (DBD) plasma regeneration was proposed to treat the indigo carmine solution. It is the first time to report ectopic regeneration of the saturated resins by non-thermal Dielectric Barrier Discharge. The adsorption/desorption efficiency, surface functional groups, structural properties, regeneration efficiency, and the intermediate products between gas and liquid phase before and after treatment were investigated. The results showed that DBD plasma could maintain the efficient adsorption performance of resins while degrading the indigo carmine adsorbed by resins. The degradation rate of indigo carmine reached 88% and the regeneration efficiency (RE) can be maintained above 85% after multi-successive regeneration cycles. The indigo carmine contaminants were decomposed by a variety of reactive radicals leading to fracture of exocyclic C=C bond, which could cause decoloration of dye solution. Based on above results, a possible degradation pathway for the indigo carmine by resin adsorption/DBD plasma treatment was proposed. Full article
(This article belongs to the Special Issue Photocatalysts for Organics Degradation)
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