The future and continuity of nanomaterials are heavily dependent on their availability and affordability. This could be achieved when cheap materials are actively employed as starting materials for nanomaterials synthesis. In this study, waste corn cob char was used as support during the preparation of the NiMo catalyst, and the effect of different char-activating techniques on the microstructure, yield and quality of carbon nanotubes (CNTs) obtained from waste polypropylene (PP) plastics using the chemical vapor deposition (CVD) technique was investigated. Properties of the catalysts and obtained nanomaterials were evaluated by XRD, SEM, N physisorption experiment, FTIR, Raman spectroscopy and TEM. Results showed improved surface properties of the NiMo catalyst supported on chemically (NiMo/AC) and physically activated char (NiMo/AC) compared to the NiMo catalyst supported on non-activated char (NiMo/AC). High-quality CNTs were deposited over NiMo/AC compared to NiMo/AC and NiMo/AC. It was also observed that different activation methods resulted in the formation of CNTs of different microstructures and yield. Optimum yield (470.0 mg CNTs/g catalyst) was obtained with NiMo/AC, while NiMo/AC gave the least product yield (70.0 mg CNTs/g catalyst) of the as-produced nanomaterials. Based on the results of the analysis, it was concluded that utilizing a cheap pyrogenic product of waste corn cob as a catalyst support in a bimetallic NiMo catalyst could offer a promising approach to mass producing CNTs and as a low-cost alternative in CNTs production from waste plastics.
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http://dx.doi.org/10.3390/polym14142898 | DOI Listing |
ACS Appl Mater Interfaces
January 2025
Institute of Experimental Physics, Faculty of Mathematics Physics and Informatics, University of Gdańsk, Wita Stwosza 57, Gdańsk 80-308, Poland.
This study examines the structure and properties of NiMo-C coatings synthesized via reactive magnetron sputtering of a NiMo alloy target in an argon/acetylene atmosphere. The coating structure evolves with carbon content from nanocrystalline, through amorphous to quasi-amorphous with a nanocolumnar structure. The nanostructure consists of metallic columns perpendicular to the substrate surrounded by an amorphous carbon shell.
View Article and Find Full Text PDFChemSusChem
January 2025
Qingdao University, College of Chemistry and Chemical Engineering, 308 Ningxia Road, Qingdao, CHINA.
Polyurethane (PU), as a thermoset polymer, is extensively utilized in various applications, such as refrigerator foams, sponges, elastomers, shoes, etc. However, the recycling of post-consumed PU poses significant challenges due to its intricate and extensive crosslinking structures. Catalytic hydrogenation is one of the most effective methods for recycling PU waste, nevertheless, there is currently a lack for a hydrogenation catalyst that is both high-performing, recyclable, and cost-effective for breaking down post-consumed PU materials.
View Article and Find Full Text PDFInorg Chem
January 2025
Henan Key Laboratory of Polyoxometalate Chemistry, College of Chemistry and Molecular Sciences, Henan University, Kaifeng, Henan 475004, P. R. China.
Amide compounds are widely present in drug molecules and natural products, which can be synthesized by acid-amine condensation. It is urgent to design new photocatalysts for achieving both nitroaromatic reduction and C-H oxidation to obtain raw materials, carboxylic acids, and aromatic amines. Herein, a novel isopolymolybdate-incorporated photoactive metal-organic framework, -TPT, was constructed by combining the oxidation catalyst [MoO], Ni(II) cation, and photosensitive ligand 2,4,6-tri(4-pyridyl)-1,3,5-triazine (TPT).
View Article and Find Full Text PDFMicrosc Res Tech
December 2024
Department of Biotechnology, College of Science, Taif University, Taif, Saudi Arabia.
In this study, a catalyst with Ni-Mo combination was synthesized using the electric heating/reductive tempering method. Nickel (II) nitrate hexahydrate and ammonium molybdate were combined in a ratio of 1.1 in this approach.
View Article and Find Full Text PDFACS Appl Mater Interfaces
December 2024
Department of Chemical and Biomolecular Engineering, Lehigh University, 111 Research Dr., Bethlehem, Pennsylvania 18015, United States.
Electrocatalytic urea oxidation reaction is a promising alternative to water oxidation for more efficient hydrogen production due to its significantly lower thermodynamic potential. However, achieving efficient electrochemical urea oxidation remains a formidable challenge, and development of an improved electrocatalyst with an optimal physicochemical and electronic structure toward urea oxidation is desired. This can be accomplished by designing a tailored two-dimensional composite with an abundance of active sites in a favorable electronic environment.
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