Pota Giulio, Venezia Virginia, Vitiello Giuseppe, Di Donato Paola, Mollo Valentina, Costantini Aniello, Avossa Joshua, Nuzzo Assunta, Piccolo Alessandro, Silvestri Brigida, Luciani Giuseppina
Department of Chemical, Materials and Production Engineering, University of Naples "Federico II", p.le V. Tecchio 80, 80125 Naples, Italy.
CSGI, Center for Colloids and Surface Science, via della Lastruccia 3, 50019 Florence, Italy.
Polymers (Basel). 2020 Apr 23;12(4):982. doi: 10.3390/polym12040982.
Humic acids (HA) exhibit fascinating multifunctional features, yet degradation phenomena as well as poor stability in aqueous environments strongly limit their use. Inorganic nanoparticles are emerging as a powerful interface for the development of robust HA bio-hybrid materials with enhanced chemical stability and tunable properties. Hybrid organic-inorganic SiO/HA nanostructures were synthesized via an in-situ sol-gel route, exploiting both physical entrapment and chemical coupling. The latter was achieved through amide bond formation between carboxyl groups of HA and the amino group of 3-aminopropyltriethoxysilane (APTS), as confirmed by Fourier-Transform Infrared (FTIR) and Nuclear Magnetic Resonance (NMR) spectroscopy. Monodisperse hybrid nanoparticles about 90 nm in diameter were obtained in both cases, yet Electron Paramagnetic Resonance (EPR) spectroscopy highlighted the different supramolecular organization of HA. The altered HA conformation was reflected in different antioxidant properties of the conjugated nanoparticles that, however, resulted in being higher than for pure HA. Our findings proved the key role of both components in defining the morphology of the final system, as well as the efficacy of the ceramic component in templating the HA supramolecular organization and consequently tuning their functional features, thus defining a green strategy for bio-waste valorization.
腐殖酸(HA)具有迷人的多功能特性,但其降解现象以及在水性环境中较差的稳定性严重限制了它们的应用。无机纳米颗粒正成为开发具有增强化学稳定性和可调性能的坚固HA生物杂化材料的强大界面。通过原位溶胶 - 凝胶法合成了有机 - 无机SiO/HA纳米结构,利用了物理包埋和化学偶联。傅里叶变换红外(FTIR)和核磁共振(NMR)光谱证实,后者是通过HA的羧基与3 - 氨丙基三乙氧基硅烷(APTS)的氨基之间形成酰胺键来实现的。在两种情况下均获得了直径约90nm的单分散杂化纳米颗粒,然而电子顺磁共振(EPR)光谱突出了HA不同的超分子组织。HA构象的改变反映在共轭纳米颗粒不同的抗氧化性能上,不过其抗氧化性能高于纯HA。我们的研究结果证明了两种组分在确定最终体系形态方面的关键作用,以及陶瓷组分在模板化HA超分子组织并因此调节其功能特性方面的功效,从而确定了一种生物废物增值的绿色策略。