The nanotubes of pure hydrogen titanate and anatase-titania have been synthesized via hydrothermal treatment of as-received anatase-titania particles. The formation mechanism of anatase-titania nanotubes via hydrothermal has been discussed in detail in view of the finger-prints produced by characterizing the intermediate and end products using various microscopic and spectroscopic techniques such as scanning electron microscope, high-resolution transmission electron microscope, X-ray diffraction, Brunauer, Emmett, and Teller specific surface-area measurement, Fourier transform infrared spectroscope, diffuse reflectance, photoluminescence, thermal gravimetric and differential thermal analyses. The obtained results strongly support the rollup mechanism, involving multiple nanosheets, for the formation of anatase-titania nanotubes with the formation of different intermediate hydrothermal products having various morphologies such as sodium titanate having aggregated rectangular block-like structures, hydrogen sodium titanate and pure hydrogen titanate having highly aggregated unresolved fine-structures containing nanotubes, and finally, the pure anatase-TiO2 nanotubes. It is demonstrated that, during the hydrothermal treatment, the nanotubes of pure hydrogen titanate are formed first coinciding with the stable solution-pH during washing, indicating the completion of ion-exchange process, and a drastic increase in the specific surface-area of the hydrothermal product. The anatase-titania nanotubes are then derived from the pure hydrogen titanate nanotubes via thermal treatment. The use of pure hydrogen titanate and anatase-titania nanotubes for an organic textile dye-removal, from an aqueous solution under the dark condition, via surface-adsorption mechanism has been demonstrated. It is shown that, the specific surface-area and the surface-charge govern the maximum dye-absorption capacity of the anatase-TiO2 nanotubes under the dark condition.
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http://dx.doi.org/10.1166/jnn.2011.3048 | DOI Listing |
J Mol Model
January 2025
Escuela Superior de Física y Matemáticas, IPN S/N, Edificio 9 de la Unidad Profesional "Adolfo López Mateos", Col. Lindavista, Alc. Gustavo A. Madero, 07738, Mexico City, Mexico.
Context: "Nanostructure of graphene-reinforced with polymethyl methacrylate" (PMMA-G), and vice versa, is investigated using its molecular structure, in the present work. The PMMA-G nanostructure was constructed by bonding PMMA with graphene nanosheet in a sense to get three different configurations. Each configuration consisted of polymeric structures with three degrees of polymerization (such as monomers, dimers, and trimers polymers, respectively).
View Article and Find Full Text PDFChem Asian J
January 2025
China Three Gorges University, Key Laboratory of Inorganic Nonmetallic Crystalline and Energy Conversion Materials, College of Materials and Chemical Engineering, China Three Gorges University, CHINA.
The Keggin clusters are one kind of the most representative molecular structures in the field of metal-oxo clusters. Although the different types of Keggin clusters with various components were reported, the research about γ-Keggin isomer remains less developed. This is ascribed to the difficulty in obtaining the stable pure γ-Keggin cluster for the structural isomerization.
View Article and Find Full Text PDFJ Colloid Interface Sci
January 2025
Institute of Micro/Nano Materials and Devices, Ningbo University of Technology, Ningbo 315211 PR China. Electronic address:
The development of efficient photocatalysts inspired by natural photosynthesis has drawn considerable interest for sustainable hydrogen (H) production. Among the various strategies for enhancing H evolution, constructing step-scheme (S-scheme) heterojunctions has attracted extensive interest, thanks to their limited charge recombination and enhanced charge transport in comparison to the traditional photocatalytic systems. Herein, we report the engineering of a novel S-scheme heterojunction by integrating ultrathin ZnInS (ZIS) nanosheets with MOF-derived N-doped NiO porous microrods (ZIS/N-NiO) toward superior photocatalytic behaviors.
View Article and Find Full Text PDFCommun Chem
January 2025
The Institute for Solid State Physics (ISSP), The University of Tokyo, Kashiwa, Chiba, 277-8581, Japan.
The discovery of fullerene following the synthesis of graphene marked a paradigm shift in chemistry. Here, we report the discovery of biycycloborane, arising from the synthesis of borophane (hydrogen boride). Uniquely, this synthesis method involves a decomposition mechanism rather than traditional atom-by-atom assembly, marking an unique approach to constructing complex borane structures.
View Article and Find Full Text PDFACS Appl Mater Interfaces
January 2025
Department of Chemistry and Materials Engineering, Kansai University, 3-3-35 Yamate-cho, Suita, Osaka 564-8680, Japan.
Hydride (H) species on oxides have been extensively studied over the past few decades because of their critical role in various catalytic processes. Their syntheses require high temperatures and the presence of hydrogen, which involves complex equipment, high energy costs, and strict safety protocols. Hydride species tend to decompose in the presence of atmospheric oxygen and water, which reduces their catalytic activities.
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