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Surface modification of TiO(2) nanoparticles with biodegradable nanocellolose and synthesis of novel polyimide/cellulose/TiO(2) membrane

In this paper, novel polyimide/cellulose/TiO(2) bionanocomposites (PI/BNCs) were prepared via a simple and inexpensive ultrasonic irradiation process. PI was synthesized by direct polycondensation reaction of novel monomer dianhydride with 4-(2-(4-aminophenyl)-1,1,1,3,3,3-hexafluoropropan-2-yl)benze...

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Detalles Bibliográficos
Autor principal: Ahmadizadegan, Hashem
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Academic Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5261836/
https://www.ncbi.nlm.nih.gov/pubmed/28068578
http://dx.doi.org/10.1016/j.jcis.2016.11.043
Descripción
Sumario:In this paper, novel polyimide/cellulose/TiO(2) bionanocomposites (PI/BNCs) were prepared via a simple and inexpensive ultrasonic irradiation process. PI was synthesized by direct polycondensation reaction of novel monomer dianhydride with 4-(2-(4-aminophenyl)-1,1,1,3,3,3-hexafluoropropan-2-yl)benzenamine. Due to the high surface energy and tendency for agglomeration the surface of nanoparticles was modified with cellulose. PI/BNCs containing 5, 10, and 15% of cellulose/TiO(2) (BNCs) were successfully fabricated through ultrasonic irradiation technique. The obtained PI/BNCs were characterized by Fourier transform-infrared (FT-IR) spectroscopy, thermogravimetry analysis, X-ray powder diffraction, field emission-scanning electron microscopy (FE-SEM), and transmission electron microscopy (TEM). Thermogravimetric analysis data indicated an increase thermal stability of the PI/BNC polymers in compared to the pure polymer. From TEM image of PI/BNCs it can be found that the surface modified TiO(2) with diametric size of less than 50 nm, uniformly dispersed in the obtained PI matrix. The results obtained from gas permeation experiments with a constant pressure setup indicated that adding cellulose/TiO(2) to the polymeric membrane structure increased the permeability of the membranes.