Por favor, use este identificador para citar o enlazar este ítem: http://hdl.handle.net/20.500.12666/875
Título : Tuning the Morphology in the Nanoscale of NH4CN Polymers Synthesized by Microwave Radiation: A Comparative Study
Autor : Pérez Fernández, Cristina
Valles González, M. P.
González Toril, Elena
Mateo Martí, Eva
De la Fuente, J. L.
Ruiz Bermejo, Marta
Palabras clave : HCN polymers;Cyanide polymerization;Microwave-driven polymerization;Nanoparticles;Nanofibers;Multifunctional materials
Fecha de publicación : 24-dic-2021
Editorial : Multidisciplinary Digital Publishing Institute (MDPI)
DOI: 10.3390/polym14010057
Versión del Editor: https://www.mdpi.com/2073-4360/14/1/57
Citación : Polymers 14(1): 57(2022)
Resumen : A systematic study is presented to explore the NH4CN polymerization induced by microwave (MW) radiation, keeping in mind the recent growing interest in these polymers in material science. Thus, a first approach through two series, varying the reaction times and the temperatures between 130 and 205 °C, was conducted. As a relevant outcome, using particular reaction conditions, polymer conversions similar to those obtained by means of conventional thermal methods were achieved, with the advantage of a very significant reduction of the reaction times. The structural properties of the end products were evaluated using compositional data, spectroscopic measurements, simultaneous thermal analysis (STA), X-ray diffraction (XRD), and scanning electron microscopy (SEM). As a result, based on the principal component analysis (PCA) from the main experimental results collected, practically only the crystallographic features and the morphologies in the nanoscale were affected by the MW-driven polymerization conditions with respect to those obtained by classical syntheses. Therefore, MW radiation allows us to tune the morphology, size and shape of the particles from the bidimensional C=N networks which are characteristic of the NH4CN polymers by an easy, fast, low-cost and green-solvent production. These new insights make these macromolecular systems attractive for exploration in current soft-matter science.
URI : http://hdl.handle.net/20.500.12666/875
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