Waste for Product Approach: The Role of the Nanomaterials in the Process

A special issue of Nanomaterials (ISSN 2079-4991). This special issue belongs to the section "Energy and Catalysis".

Deadline for manuscript submissions: 30 January 2026 | Viewed by 1172

Special Issue Editor


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Guest Editor
Faculty of Non-Ferrous Metals, AGH University of Science and Technology, Al. A. Mickiewicza 30, 30-059 Krakow, Poland
Interests: microreactor system; nanoparticles; nanomaterials; clusters; metalorganic; complexes; kinetics; catalyst; metal determination; separation
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Special Issue Information

Dear Colleagues,

Nowadays, a big challenge is finding new metal resources or methods for their efficient recovery from waste solutions. In this collection, we propose the “Waste for Product” (W4P) approach as a vision for better and faster metals recovery and processing of metals directly from waste solutions (synthetic as well as industrial sample) to new products. In the W4P approach, it is necessary to take into account the wealth of products that we can produce, considering the various sources of waste solutions (mining, chemistry, pharmacy). As many types of waste solutions (specificity of their composition) as we have, we can obtain the same number of different product properties, even if the same metals are present in the waste solution. This, in turn, provides a great opportunity to create completely new materials with unique properties.

This issue presents a broad range of subjects in which nanomaterials are substrate, intermediate, or final products of the recovery process. The conducted research should also include information on the estimated costs/benefits resulting from the use of the W4P approach. Articles that include concept proof in the form of confirmation of synthesized product applications for selected areas (catalysis, chemistry, pharmacy, etc.), as well as commentary on the environmental impact of the proposed solution, are also welcome.

Dr. Magdalena Luty-Błocho
Guest Editor

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Keywords

  • nanomaterials
  • catalyst
  • pharmaceutical waste
  • mining waste
  • metals recovery

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Published Papers (1 paper)

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Research

16 pages, 5125 KB  
Article
One-Step Synthesis of Ultra-Small RhNPs in the Microreactor System and Their Deposition on ACF for Catalytic Conversion of 4–Nitrophenol to 4–Aminophenol
by Adrianna Pach, Konrad Wojtaszek, Ahmed Ibrahim Elhadad, Tomasz Michałek, Anna Kula and Magdalena Luty-Błocho
Nanomaterials 2025, 15(17), 1375; https://doi.org/10.3390/nano15171375 - 5 Sep 2025
Viewed by 704
Abstract
The rising demand for platinum-group metals, driven by their essential applications in catalysis, energy storage, and chemical conversion, underscores the need to identify new sources for their recovery. Waste solutions originating from industrial processes offer a promising alternative source of noble metals. However, [...] Read more.
The rising demand for platinum-group metals, driven by their essential applications in catalysis, energy storage, and chemical conversion, underscores the need to identify new sources for their recovery. Waste solutions originating from industrial processes offer a promising alternative source of noble metals. However, due to their typically low concentrations, effective recovery requires a highly targeted approach. In this study, we present a synthetic waste solution containing trace amount of Rh(III) ions as both a medium for metal ion recovery and a direct precursor for catalyst synthesis. Using a bimodal water–ethanol solvent system, ultra-small rhodium nanoparticles were synthesized and subsequently immobilized onto activated carbon fibers (ACFs) within a microreactor system. The resulting Rh@ACF catalyst demonstrated high efficiency in the reduction of 4-nitrophenol (4-NP) to 4-aminophenol (4-AP), serving as a model catalytic reaction. The Rh@ACF catalyst, containing 4.24 µg Rh per milligram of sample, exhibited notable catalytic activity, achieving 75% conversion of 4-NP to 4-AP within 1 h. Full conversion to 4-AP was also reached within 5 min, but requires extra NaBH4 addition to the catalytic mixture. Full article
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