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<title>Polímeros (POLYMERS)</title>
<link>https://hdl.handle.net/10259/4313</link>
<description/>
<pubDate>Fri, 17 Apr 2026 04:40:33 GMT</pubDate>
<dc:date>2026-04-17T04:40:33Z</dc:date>
<item>
<title>Coumarin-inspired light-responsive thermoplastic adhesives for recyclable multilayer packaging</title>
<link>https://hdl.handle.net/10259/11488</link>
<description>Coumarin-inspired light-responsive thermoplastic adhesives for recyclable multilayer packaging
Sedano Labrador, Carlos; Herrero, Manuel; Trigo López, Miriam; Rodríguez Pérez, Miguel Ángel .; Merino, Juan Carlos; García Pérez, José Miguel; Vallejos Calzada, Saúl; Núñez-Carrero, Karina C.
Multilayer plastic packaging offers essential barrier and mechanical properties for food preservation, but its complex structure prevents effective recycling. Here, we report a light-responsive thermoplastic adhesive designed to enable on-demand separation of polymer layers in multilayer packaging. The adhesive adopts a triblock architecture with terminal blocks compatible with polyethylene (PE) and polyamide (PA), and a central segment functionalised with coumarin-based photoremovable groups. Upon ultraviolet (UV) exposure, the adhesive undergoes complete molecular breakdown, triggering clean delamination without solvents or mechanical force. Fabricated PE – photosensitive adhesive – PA films demonstrated superior adhesion performance compared to a commercial benchmark during service life, and efficient separation upon irradiation, as confirmed by Fourier transform infrared (FTIR) spectroscopy, microscopy, and T-peel testing. Life cycle assessment revealed that, while the laboratory-scale synthesis has higher environmental costs, the impact is offset after a single reuse cycle in projected industrial conditions, reaching up to 80% reduction after six cycles. This approach provides a scalable strategy to reconcile performance and recyclability in multilayer packaging.
</description>
<pubDate>Thu, 01 Jan 2026 00:00:00 GMT</pubDate>
<guid isPermaLink="false">https://hdl.handle.net/10259/11488</guid>
<dc:date>2026-01-01T00:00:00Z</dc:date>
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<item>
<title>Naked-eye detection of Listeria monocytogenes using smart chromogenic polymers with tuneable surface morphologies</title>
<link>https://hdl.handle.net/10259/11487</link>
<description>Naked-eye detection of Listeria monocytogenes using smart chromogenic polymers with tuneable surface morphologies
Arnáiz Alonso, Ana; Melero Gil, Beatriz; Trigo López, Miriam; Mendía Jalón, Aránzazu; Fuente Vivas, Dalia de la; Iñigo Martínez, María Emilia; Gómez Cuadrado, Laura; Ibeas Cortes, Saturnino; Vallejos Calzada, Saúl
Listeria monocytogenes is a major foodborne pathogen associated with listeriosis, with a mortality rate of up to 30 %. Conventional detection methods are often time-consuming and require sophisticated equipment or complementary techniques to ensure sensitivity and specificity. This study presents a smart chromogenic polymeric sensor for the rapid detection of L. monocytogenes based on the activity of phosphatidylinositol-specific phospholipase C (PI-PLC). Six hydrophilic polymer films with identical compositions but different surface properties were developed, incorporating a chromogenic substrate that produces a visible colour change upon enzymatic hydrolysis, allowing the direct visual identification of L. monocytogenes. The sensitivity and specificity were assessed against a panel of foodborne bacteria, with detection limits of 104 CFUs/mL. Among the tested materials, NC2sf, Ff, and Sf showed the highest sensitivity and limited cross-reactivity with L. ivanovii, Staphylococcus aureus, and Bacillus cereus. Biocompatibility assays in HepG2 cells confirmed acceptable cytocompatibility, underscoring the importance of substrate selection for minimising adverse cellular effects. A proof-of-concept test on chicken breast slices and fresh-cut melon demonstrated the specific detection of L. monocytogenes and clear discrimination from non-pathogenic L. innocua, confirming the robustness and selectivity of the system. Finally, a Life Cycle Assessment highlighted the environmental impact of the sensing materials and provided insights into their potential pre-industrial scalability.
</description>
<pubDate>Sun, 01 Mar 2026 00:00:00 GMT</pubDate>
<guid isPermaLink="false">https://hdl.handle.net/10259/11487</guid>
<dc:date>2026-03-01T00:00:00Z</dc:date>
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<item>
<title>Multifunctional smart polymers and citizen science for a comprehensive approach to nitrate pollution: Curative and preventive strategies</title>
<link>https://hdl.handle.net/10259/11026</link>
<description>Multifunctional smart polymers and citizen science for a comprehensive approach to nitrate pollution: Curative and preventive strategies
Vallejo García, Jorge Lucas; Hernández Ruiz, Raquel; Torija López, Alba; Trigo López, Miriam; Ibeas Cortes, Saturnino; Gómez Cuadrado, Laura; Martel Martín, Sonia; Barros García, Rocío; Vallejos Calzada, Saúl
This work presents the development and evaluation of a multifunctional smart polymer (FNO₃)&#13;
for the extraction and detection of nitrates in drinking water. A total of 250 tap water samples&#13;
from various localities were analyzed, revealing nitrate concentrations that in some cases doubled&#13;
the legal limit (up to 100 mg⋅L⁻¹). FNO₃, composed of 49.75 mol% NNZA monomer with high&#13;
anion-exchange capacity, exhibited a maximum nitrate adsorption capacity (qmax) of&#13;
164 ± 5 mg⋅g⁻¹ , which is 3.6 times greater than that of commercial resins. The polymer&#13;
demonstrated significant swelling in water (~2014 ± 152 %) and incorporated a sensing functionality&#13;
via a fluorometric monomer, enabling visual detection when saturation occurs. Fluorescence&#13;
response studies yielded a limit of detection (LOD) of 4.26 mg⋅L⁻¹ and a limit of&#13;
quantification (LOQ) of 12.92 mg⋅L⁻¹ , values that are below the regulatory thresholds established&#13;
by European and Spanish legislation for nitrates in drinking water. The material was tested&#13;
through multiple adsorption-regeneration cycles using domestic saline solutions, maintaining&#13;
stable efficiency. Interference studies indicated that carbonates present in hard water partially&#13;
reduce adsorption effectiveness. Life Cycle Assessment (LCA) identified the structural materials and&#13;
functional monomers as the main contributors to environmental impact, while reuse and polymer&#13;
application offer environmental benefits due to nitrate recovery. Additionally, in vitro toxicological&#13;
assays with HepG2 cells confirmed the absence of cytotoxicity, supporting the polymer’s&#13;
viability for safe water treatment applications.
</description>
<pubDate>Sat, 01 Nov 2025 00:00:00 GMT</pubDate>
<guid isPermaLink="false">https://hdl.handle.net/10259/11026</guid>
<dc:date>2025-11-01T00:00:00Z</dc:date>
</item>
<item>
<title>UBU-Polymers Research Group 21032024</title>
<link>https://hdl.handle.net/10259/11017</link>
<description>UBU-Polymers Research Group 21032024
Vallejo García, Jorge Lucas; Trigo López, Miriam; Ibeas Cortes, Saturnino; García García, Félix Clemente; Busto Núñez, Mª Dolores; Núñez-Carrero, Karina C.; Alonso-Pastor, Luis E.; Vallejos Calzada, Saúl
This work presents a new polymeric material in the form of a film (FLAC) containing immobilized laccase enzyme&#13;
through diazo bonds, designed for the degradation of indigo carmine dye, which is highly toxic and commonly&#13;
found in wastewater from the textile industry. The immobilization of the enzyme in the film was characterized by&#13;
SEM, FT-IR, DSC, TGA and EDXS. The degradation of the dye by FLAC initiates in the presence of a mediator due&#13;
to the high redox potential of the dye. Six natural mediators (ferulic acid, syringaldazine, guaiacol, eugenol,&#13;
thymol, and p-coumaric acid) were tested, and complete degradation of the dye was achieved in 180 min, with a&#13;
mediator concentration of 1 ppm (syringaldazine) and a dye concentration of 10 ppm. A novelty in this study is&#13;
the short exposure time of the dye-mediator solution to FLAC (15 min) which allowed the degradation process to&#13;
continue autonomously after the film was removed. Additionally, it was observed that the material was more&#13;
effective in the presence of textile washing products, achieving over 99 % degradation in 40 min, surpassing its&#13;
efficacy in distilled water. Regarding reusability, the material retained &gt;90 % of its activity after five cycles of&#13;
use and washing. Life Cycle Assessment (LCA) and Techno-Economic Analysis (TEA) identified key levers for&#13;
techno-economic and environmental viability: shorten cycle time (surfactant media), maximise re-use and percycle&#13;
volume/concentration, implement solvent recovery, and energy decarbonization thereby outlining a&#13;
roadmap to sustainable scale-up.
</description>
<pubDate>Tue, 28 Oct 2025 00:00:00 GMT</pubDate>
<guid isPermaLink="false">https://hdl.handle.net/10259/11017</guid>
<dc:date>2025-10-28T00:00:00Z</dc:date>
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