Preparation of Chitosan/Poly(vinyl Alcohol) Blend Nanofibers Containing Ag-SiO2 Nanoparticles via Electrospinning

2011 ◽  
Vol 675-677 ◽  
pp. 271-274
Author(s):  
Fang Fang Zuo ◽  
Bo Wen Cheng ◽  
Wei Min Kang ◽  
Yu Hao Ma

Chitosan (CS) / poly(vinyl alcohol) (PVA) blend nanofibers containing Ag-SiO2 nanoparticles (CS/PVA/Ag-SiO2 nanofibers) were successfully prepared by electrospinning using formic acid (HCOOH) as solvent in this paper. The morphology, diameter and structure of the electrospun nanofibers were examined by scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR) and X-ray Photoelectron Spectroscopy (XPS). And the diameter distribution of the nanofibers was measured by Image-Pro Plus. The results showed that the ideal nanofibers with the diameter in 85-165 nm can be obtained with the proper technical parameters as follows: the spinning voltage at 40 kV, the extruding speed at 0.5 mL/h and the collecting distance at 200 mm. The CS/PVA/Ag-SiO2 nanofibers will present potential applications in wound dressing and bandage etc.

2012 ◽  
Vol 602-604 ◽  
pp. 157-160
Author(s):  
Wei Min Kang ◽  
Jing Yan ◽  
Bo Wen Cheng

Polyurethane-poly (vinyl alcohol)/chitosan (PU-PVA/CS) blend nanofiber nonwovens were successfully prepared by coelectrospinning in this paper. The morphology, diameter and structure of the electrospun nanomaterials were examined by SEM and FITR, and their mechanical properties were tested. The diameter distribution of the nanofibers was measured by Image-Pro Plus. The results show that the ideal nanofibers with the diameter in 50-350 nm can be obtained with the proper technical parameters of PU and PVA/CS nanofibers as follows: the spinning voltage at 30 kV and 40 kV, the extruding speed at 6 mL/h and 0.5 ml/h, the collecting distance at 150 mm and 200 mm, respectively.


2010 ◽  
Vol 152-153 ◽  
pp. 1333-1336 ◽  
Author(s):  
Xu Pin Zhuang ◽  
Zheng Li ◽  
Wei Min Kang ◽  
Bo Wen Cheng

New chitosan/poly (vinyl alcohol) (PVA) nanofibers functionalized with silver nanoparticles were electrospun using solutions of PVA blended with silver nanoparticles-chitosan composites. The structure of the electrospun fibers were studied with the aid of scanning electron microscopy, transmission electron microscopy, and X-ray photoelectron spectroscopy. The results indicated that the electrospun fibers smoothly with 220 to 650 nm diameter, and the silver nanoparticles were successfully embed into the fibers which show high antibacterial activity against E.coli.


2016 ◽  
Vol 701 ◽  
pp. 265-269 ◽  
Author(s):  
Md Shariful Islam ◽  
Fayeka Mansura ◽  
Amalina Muhammad Afifi ◽  
Bee Chin Ang

In this study, poly (vinyl alcohol) / chitosan blend nanofibers were synthesized by electrospinning process in different polyvinyl alcohol and chitosan weight ratios. The nanofibers were characterized by scanning electron microscopy (SEM), Fourier transform infrared (FTIR) and X-ray diffraction (XRD). SEM images showed that, 50:50 poly vinyl alcohol/chitosan blend was the ideal ratio for producing beadless nanofiber. The average diameter of the beadless nanofiber was found to be 123 nm. FTIR and XRD results demonstrated the presence of intermolecular hydrogen bonding between the molecules of poly vinyl alcohol and chitosan.


2013 ◽  
Vol 747 ◽  
pp. 405-408
Author(s):  
Yuan Hsiang Yu ◽  
Chih Jie Jan

A series of poly (vinyl alcohol) (PVA)/functionalized graphene oxide (FGO) nanofibers with low feeding ratios of FGO to PVA were fabricated by electrospinning method. In this study, the prepared PVA/FGO nanocomposites were dispersed in water phase followed by electrospinning treatment under different operational parameters (i.e., applied voltage, feeding rate and FGO contents) to give nanofibers of various diameters and morphologies. The morphology, diameter and structure of electrospun nanofibers and FGO were investigated by Fourier transform infrared (FT-IR) spectroscopy, X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), (TGA) and differential scanning calorimetry (DSC). SEM images showed that the morphologies of the nanofibers were improved by the incorporation of FGO at a low loading content (e.g., 0.1~0.5 wt %) as compared to pure electrospun PVA. The crystallinity and thermal stability of PVA/FGO nanofibers were also studied.


Author(s):  
Wenxiu Wang ◽  
Hui Xu ◽  
Jian Chen ◽  
Yuanfang Shen ◽  
Imre Bertóti ◽  
...  

Graphene oxide foams with a wide range of poly (vinyl alcohol) contents were synthesized by freeze casting, and then thermally reduced at 300ºC in argon atmosphere. Their thermal stability, microstructure, composition and chemical states of constituents, mechanical and electrical properties were investigated by X-ray diffraction, scanning electron microscopy, X-ray photoelectron spectroscopy, thermogravimetry, compressive testing and electrochemical analysis. The results indicated that the PVA content highly influenced the crystallinity and microstructure, resulting in different mechanical properties. After thermal reduction, not only graphene oxide was reduced to graphene, but also PVA was subjected to partial pyrolysis. With the increase of the PVA content, the intensity of the sp2 C-C bond decreased while the sp3 C-C bond increased. Although the mechanical properties decreased after thermal reduction, the composite foams still showed high cyclic structure stability up to 18 % compression strain. Meanwhile, the reduced foams exhibited high electrical conductivity. Applying as anodes in lithium ion battery, the initial discharge capacity for the foams can reach 1822 mA h g-1 and it remained more than 330 mA h g-1 after 50 cycles.


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