Hromádko Luděk, Koudelková Eva, Bulánek Roman, Macak Jan M
Center of Materials and Nanotechnologies, Faculty of Chemical Technology, University of Pardubice, Nam. Cs. Legii 565, Pardubice 530 02, Czech Republic.
Department of Physical Chemistry, Faculty of Chemical Technology, University of Pardubice, Studentska 573, Pardubice 530 02, Czech Republic.
ACS Omega. 2017 Aug 28;2(8):5052-5059. doi: 10.1021/acsomega.7b00770. eCollection 2017 Aug 31.
Facile and innovative route for large-scale synthesis of SiO fibers with excellent textural properties and HO adsorption performance is presented. At first, a three-dimensional network of SiO precursor fibers was produced from tailored spun solutions (without any toxic elements and surfactants) by centrifugal spinning, which is a very modern fiber-synthesis technique, with numerous advantages over electrospinning. Upon thermal annealing of the precursor fibers, mesoporous amorphous SiO fibers with an ultrahigh surface area of up to 824 m/g and pore size distribution in the range of 2-10 nm were produced. Owing to the high number of OH groups available on the surface, the produced SiO fibers showed significantly better performance in HO adsorption compared to that of the reference silicagel.
本文提出了一种简便且创新的路线,用于大规模合成具有优异结构性能和水吸附性能的SiO纤维。首先,通过离心纺丝从定制的纺丝溶液(不含任何有毒元素和表面活性剂)中制备出SiO前驱体纤维的三维网络,离心纺丝是一种非常现代的纤维合成技术,与静电纺丝相比具有许多优势。对前驱体纤维进行热退火后,制备出了具有高达824 m²/g的超高比表面积和2-10 nm孔径分布的介孔无定形SiO纤维。由于表面存在大量的羟基,所制备的SiO纤维在水吸附方面表现出比参比硅胶显著更好的性能。