Superhydrophobic micro-nanofibers from PHBV-SiO2 biopolymer composites produced by electrospinning

Saad Rabbani, Reza Jafari, Gelareh Momen
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引用次数: 1

Abstract

Electrospinning is a relatively simple technique for producing continuous fibers of various sizes and morphologies. In this study, an intrinsically hydrophilic poly(3-hydroxybutarate-co-3-hydroxyvalerate) (PHBV) biopolymer strain was electrospun from a solution under optimal processing conditions to produce bilayers of beadless micro-fibers and beaded nano-fibers. The fibrous mats produced from the pure PHBV solution exhibited hydrophilicity with complete wetting. Incorporation of polydimethylsiloxane (PDMS) treated silica into the electrospinning solutions resulted in a non-wetting state with increased fiber roughness and enhanced porosity; however, the fiber mats displayed high water droplet-adhesion. The SiO2–incorporated fibrous mats were then treated with stearic acid at an activation temperature of 80 °C. This treatment caused fiber surface plasticization, creating a tertiary hierarchical roughness owing to the interaction of PHBV chains with the polar carboxyl groups of the stearic acid. Scanning electron microscopy was used to assess the influence of the electrospinning process parameters and the incorporation of nanoparticles on surface morphology of the fibers; energy dispersive X-ray spectroscopy confirmed the presence of SiO2 nanoparticles. Fourier transform infrared spectroscopy was performed to study the incorporation of SiO2 and the interaction of stearic acid with PHBV at various concentrations. The chemical interaction between stearic acid and PHBV was confirmed, while SiO2 nanoparticles were successfully incorporated into the PHBV fibers at concentrations up to 4.5% by weight. The incorporation of nanoparticles and plasticization altered the thermal properties of PHBV and a decrease in crystalline fraction was observed. The stearic acid modified bilayers produced from the micro-nano-fibrous composites showed very low water droplet sticking, a roll off angle of approximately 4° and a high static contact angle of approximately 155° were achieved.

Graphical Abstract

静电纺丝法制备PHBV-SiO2生物聚合物复合材料超疏水微纳米纤维
静电纺丝是一种生产各种尺寸和形态的连续纤维的相对简单的技术。在本研究中,在最佳工艺条件下,从溶液中静电纺丝制备了一种具有亲水性的聚(3-羟基丁酸酯-co-3-羟基戊酸酯)(PHBV)生物聚合物菌株,制备了双层无头微纤维和珠状纳米纤维。由纯PHBV溶液制备的纤维席具有完全润湿的亲水性。将聚二甲基硅氧烷(PDMS)处理过的二氧化硅掺入静电纺丝溶液中,使纤维处于非润湿状态,纤维粗糙度增加,孔隙率提高;然而,纤维垫表现出较高的水滴粘附性。然后用硬脂酸在80℃的活化温度下处理二氧化硅纤维垫。这种处理导致纤维表面塑化,由于PHBV链与硬脂酸的极性羧基相互作用而产生三级层次粗糙度。采用扫描电镜观察了静电纺丝工艺参数和纳米颗粒掺入对纤维表面形貌的影响;能量色散x射线光谱证实了SiO2纳米颗粒的存在。傅里叶变换红外光谱研究了SiO2的掺入以及硬脂酸与PHBV在不同浓度下的相互作用。硬脂酸与PHBV之间的化学相互作用得到了证实,而二氧化硅纳米颗粒以4.5%的重量浓度成功地掺入到PHBV纤维中。纳米颗粒的掺入和塑化改变了PHBV的热性能,晶体分数降低。由硬脂酸修饰的微纳纤维复合材料制备的双层膜具有极低的水滴粘附,滚脱角约为4°,静态接触角约为155°。图形抽象
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