Nanoscale Material Catalysis for Environmental Protection

A special issue of Nanomaterials (ISSN 2079-4991). This special issue belongs to the section "Environmental Nanoscience and Nanotechnology".

Deadline for manuscript submissions: 23 May 2025 | Viewed by 2344

Special Issue Editor


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Guest Editor
School of Ecology and Environment, Zhengzhou University, No.100 Science Avenue, High-Tech District, Zhengzhou 450001, China
Interests: environmental catalysis; air pollutant removal; environment function material; carbon dioxide conversion

Special Issue Information

Dear Colleagues,

Nanoscale material catalysis is actively studied in the field of environmental protection. It has great potential and unique superiority in various aspects such as air pollutant elimination, wastewater purification, soil remediation, waste disposal, and CO2 conversion. The issues of how to synthesize efficient and highly selective catalysts and reveal the reaction/ inactivation are important topics in this field.

This Special Issue aims to report the latest innovative research and development in nanoscale material catalysis for the environmental protection field, covering a broad range of topics, including the design, synthesis, and application of nanoscale catalysts for pollutant removal or conversion in air, water, and soil. Revealing the related reaction/deactivation mechanism using various experimental and theoretical calculation means is also encouraged. We welcome contributions from all related groups that contribute to our understanding of this exciting and rapidly advancing field.

In this Special Issue, original research articles and reviews are welcome. Research areas may include (but are not limited to) the following:

  • Nanoscale catalyst synthesis, characterization for environmental applications.
  • Catalytic mechanisms and strategies for catalyst activation and regeneration.
  • Catalytic strategies aimed at abating environmental pollutants, including air pollutants (such as nitrogen oxides and volatile organic compounds), water pollutants, and soil pollutants.
  • Catalytic reactions that adeptly transform CO2 into valuable and useful products.

We look forward to receiving your contributions.

Dr. Wenjie Li
Guest Editor

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Keywords

  • nanoscale materials
  • environmental catalysis
  • pollution control
  • gas purification
  • water treatment
  • carbon dioxide catalytic conversion
  • electrocatalysis
  • photocatalysis
  • catalytic mechanism
  • air pollutants

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Published Papers (2 papers)

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Research

17 pages, 27979 KiB  
Article
Effect of Chemical Polishing on the Formation of TiO2 Nanotube Arrays Using Ti Mesh as a Raw Material
by Wanshun Li, Shiqiu Zhang and Fei Li
Nanomaterials 2024, 14(23), 1893; https://doi.org/10.3390/nano14231893 - 26 Nov 2024
Viewed by 381
Abstract
As a unique form of TiO2, TiO2 nanotube arrays (TiO2NTAs) have been widely used. TiO2NTAs are usually prepared by Ti foil, with little research reporting its preparation by Ti mesh. In this paper, TiO2NTAs [...] Read more.
As a unique form of TiO2, TiO2 nanotube arrays (TiO2NTAs) have been widely used. TiO2NTAs are usually prepared by Ti foil, with little research reporting its preparation by Ti mesh. In this paper, TiO2NTAs are prepared on a Ti mesh surface via an anodic oxidation method in the F-containing electrolyte. The optimal parameters for the synthesis of TiO2NTAs are as follows: the solvent is ethylene glycol and water; the electrolyte is NH4F (0.175 mol/L); the voltage is 20 V; and the anodic oxidation time is 40 min without chemical polishing. However, there is a strange phenomenon where the nanotube arrays grow only at the intersection of Ti wires, which may be caused by chemical polishing, and the other areas, where TiO2NTAs cannot be observed on the surface of Ti mesh, are covered by a dense TiO2 film. New impurities (the hydrate of TiO2 or other products) introduced by chemical polishing and attaching to the surface of the Ti mesh reduce the current of anodic oxidation and further inhibit the growth of TiO2 nanotubes. Hence, under laboratory conditions, for commercially well-preserved Ti mesh, there is no necessity for chemical polishing. The formation of TiO2NTAs includes growth and crystallization processes. For the growth process, F ions corrode the dense TiO2 film on the surface of Ti mesh to form soluble complexes ([TiF6]2−), and the tiny pores remain on the surface of Ti mesh. Given the basic photoelectrochemical measurements, TiO2NTAs without chemical polishing have better properties. Full article
(This article belongs to the Special Issue Nanoscale Material Catalysis for Environmental Protection)
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14 pages, 9321 KiB  
Article
One-Pot Synthesis of Cellulose-Based Carbon Aerogel Loaded with TiO2 and g-C3N4 and Its Photocatalytic Degradation of Rhodamine B
by Fangqin Liu, Mingjie Fan, Xia Liu and Jinyang Chen
Nanomaterials 2024, 14(13), 1141; https://doi.org/10.3390/nano14131141 - 2 Jul 2024
Cited by 1 | Viewed by 1218
Abstract
A cellulose-based carbon aerogel (CTN) loaded with titanium dioxide (TiO2) and graphitic carbon nitride (g-C3N4) was prepared using sol–gel, freeze-drying, and high-temperature carbonization methods. The formation of the sol–gel was carried out through a one-pot method using [...] Read more.
A cellulose-based carbon aerogel (CTN) loaded with titanium dioxide (TiO2) and graphitic carbon nitride (g-C3N4) was prepared using sol–gel, freeze-drying, and high-temperature carbonization methods. The formation of the sol–gel was carried out through a one-pot method using refining papermaking pulp, tetrabutyl titanate, and urea as raw materials and hectorite as a cross-linking and reinforcing agent. Due to the cross-linking ability of hectorite, the carbonized aerogel maintained a porous structure and had a large specific surface area with low density (0.0209 g/cm3). The analysis of XRD, XPS, and Raman spectra revealed that the titanium dioxide (TiO2) and graphitic carbon nitride (g-C3N4) were uniformly distributed in the CTN, while TEM and SEM observations demonstrated the uniformly distributed three-dimensional porous structure of CTN. The photocatalytic activity of the CTN was determined according to its ability to degrade rhodamine B. The removal rate reached 89% under visible light after 120 min. In addition, the CTN was still stable after five reuse cycles. The proposed catalyst exhibits excellent photocatalytic performance under visible light conditions. Full article
(This article belongs to the Special Issue Nanoscale Material Catalysis for Environmental Protection)
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