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Supercritical CO2 dried chitosan nanoparticles: production and characterization

机译:超临界CO2干燥的壳聚糖纳米粒子:生产和表征

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摘要

Herein are reported the production and characteristics of chitosan nanoparticles that go through supercritical CO2 drying. First, chitosan nanoparticles in aqueous colloidal suspension were produced by ionic crosslinking with sodium tripolyphosphate. The produced nanoparticles have a surface charge (ζ-potential) of +27 mV and an average diameter of approximately 100 nm, measured by dynamic light scattering and field emission-scanning electron microscopy observations. The liquid phase of the nanoparticle suspension was replaced successively with ethanol and supercritical CO2 to produce dried chitosan nanoparticles finally. The main characteristics of the obtained nanoparticles were determined by diverse analytical techniques. Infrared spectroscopy, solid-state 13C nuclear magnetic resonance and X-ray diffraction studies were performed to explore possible physicochemical changes induced by the drying procedure. Also, the thermal stability of the dry chitosan nanoparticles was determined by thermogravimetric assay and dynamic scanning calorimetry. Structural properties were analyzed and compared with lyophilized nanoparticles finding that the supercritically dried chitosan nanoparticles have a surface area an order of magnitude higher. Microscopy images showed that the supercritically dried chitosan nanoparticles have a porous conglomerated structure, suggesting that there is particle aggregation through the drying process. Notwithstanding, the dry chitosan nanoparticles resuspended in the dilute acid medium readily; microscopy observations showed that the size of the resuspended particles remains in the nanoscale range. The proposed procedure is able to furnish dried chitosan nanoparticles with structural characteristics and functional properties that are appealing for their use in diverse applications.
机译:本文报道了通过超临界CO 2干燥的壳聚糖纳米颗粒的生产和特征。首先,通过与三聚磷酸钠进行离子交联来制备胶体悬浮液中的壳聚糖纳米颗粒。所产生的纳米粒子具有+27 mV的表面电荷(ζ电位),并且通过动态光散射和场发射扫描电子显微镜观察测得的平均直径约为100 nm。依次用乙醇和超临界CO 2代替纳米颗粒悬浮液的液相,以最终产生干燥的壳聚糖纳米颗粒。所获得的纳米颗粒的主要特征通过多种分析技术确定。进行了红外光谱,固态13 C核磁共振和X射线衍射研究,以探讨由干燥过程引起的可能的理化变化。同样,通过热重分析和动态扫描量热法确定了干燥的壳聚糖纳米颗粒的热稳定性。分析了结构性质,并将其与冻干的纳米颗粒进行比较,发现超临界干燥的壳聚糖纳米颗粒的表面积高出一个数量级。显微镜图像显示,超临界干燥的壳聚糖纳米颗粒具有多孔的聚集结构,表明在干燥过程中存在颗粒聚集。尽管如此,干燥的壳聚糖纳米颗粒仍容易重悬于稀酸介质中;显微镜观察显示,重悬浮颗粒的尺寸保持在纳米范围内。所提出的方法能够提供具有特征性和功能性的干燥的壳聚糖纳米颗粒,其吸引了它们在各种应用中的使用。

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