Shili Xiao

Facile immobilization of gold nanoparticles into electrospun polyethyleneimine/polyvinyl alcohol nanofibers for catalytic applications

We report a facile approach to immobilizing gold nanoparticles (AuNPs) into electrospun polyethyleneimine (PEI)/polyvinyl alcohol (PVA) nanofibers for catalytic applications. In this study, electrospun PEI/PVA nanofibers with a mean diameter of 490 nm were first crosslinked with glutaraldehyde vapor to render them water stable. Then, the water-insoluble nanofibrous mats were used as nanoreactors to complex AuCl4− anions via binding with the free amine groups of PEI for subsequent formation and immobilization of AuNPs. The formed AuNPs with a diameter of 11.8 nm within the nanofibers do not significantly change the morphology of the nanofibers; while importantly the mechanical property of the fibers was greatly improved compared to the crosslinked fibers without AuNPs. Scanning electron microscopy, Fourier transform infrared spectroscopy, transmission electron microscopy, energy dispersive spectroscopy, and thermogravimetric analysis were used to characterize these hybrid nanofibers. Furthermore, we show that the AuNP-containing nanofibers display an excellent catalytic activity and reusability for the transformation of 4-nitrophenol to 4-aminophenol. The present approach to fabricating AuNP-containing nanofibers may be extended for producing other nanoparticle-containing composite nanofibrous materials for various applications in catalysis, sensing, and biomedical sciences.

Fabrication of multiwalled carbon nanotube-reinforced electrospun polymer nanofibers containing zero-valent iron nanoparticles for environmental applications

A new approach to immobilizing zero-valent iron nanoparticles (ZVI NPs) into electrospun polymer nanofibers with enhanced mechanical properties for environmental applications is presented. In this approach, multiwalled carbon nanotubes (MWCNTs) are mixed with polyacrylic acid (PAA)/polyvinyl alcohol (PVA) mixture polymer solution for subsequent electrospinning to form uniform nanofibers. The MWCNT-incorporated PAA/PVA nanofibers are crosslinked and then used as a nanoreactor to complex Fe(III) ions through binding with the PAA carboxyl groups for the reductive formation of ZVI NPs. The MWCNT-incorporated PAA/PVA nanofibers before and after immobilization with ZVI NPs are characterized using scanning electron microscopy, energy dispersive spectroscopy, transmission electron microscopy, Fourier transform infrared spectroscopy, thermogravimetric analysis, and mechanical property measurements. We show that the mechanical properties of uniform nanofibrous mats with and without ZVI NPs are significantly enhanced even with only 1.0 wt% MWCNTs incorporated. The MWCNT-reinforced PAA/PVA nanofibrous mats containing ZVI NPs (1.6 nm) display excellent capability to decolorize model dyes such as methyl blue, acridine orange, and acid fuchsine with a decoloration percentage of more than 90%. Likewise, the same nanofibrous mats are found to be able to effectively degrade trichloroethylene, a model chlorinated hydrocarbon contaminant, with a degradation efficiency approaching 93%. The MWCNT-reinforced PAA/PVA nanofibrous mats may be used for generating other functionalized nanofiber-based complex materials with enhanced mechanical properties for applications in environmental remediation, catalysis, sensing, and biomedical sciences.

Polyelectrolyte Multilayer-Assisted Immobilization of Zero-Valent Iron Nanoparticles onto Polymer Nanofibers for Potential Environmental Applications

We report a facile approach to synthesizing and immobilizing zero-valent iron nanoparticles (ZVI NPs) onto polyelectrolyte (PE) multilayer-assembled electrospun polymer nanofibers for potential environmental applications. In this approach, negatively charged cellulose acetate (CA) nanofibers fabricated by electrospinning were assembled with multilayers of poly(diallyldimethylammonium chloride) (PDADMAC) and polyacrylic acid (PAA) through electrostatic layer-by-layer assembly. The formed PAA/PDADMAC multilayers onto CA nanofibers were then used as a nanoreactor to complex Fe(II) ions through the binding with the free carboxyl groups of PAA for subsequent reductive formation of ZVI NPs. Combined scanning electron microscopy, transmission electron microscopy, energy dispersive spectroscopy, Fourier transform infrared spectroscopy, and thermogravimetry analysis studies demonstrate that the ZVI NPs are successfully synthesized and uniformly distributed into the PE multilayers assembled onto the CA nanofibers. The produced hybrid nanofibrous mats containing ZVI NPs were found to exhibit superior capability to decolorize acid fuchsin, an organic dye in dyeing wastewater. We show that the loading capacity of ZVI NPs can be tuned by changing the number of PE layers and the cycles of binding/reduction process. Increasing the number of the binding/reduction cycles leads to a slight bigger size of the ZVI NPs, which is not beneficial for improving the reactivity of ZVI NPs. The present approach to synthesizing and immobilizing ZVI NPs onto polymer nanofibers opens a new avenue to fabricating various fiber-based composite materials with a high surface area to volume ratio for environmental, catalytic, and sensing applications.

Fabrication and characterization of water-stable electrospun polyethyleneimine/polyvinyl alcohol nanofibers with super dye sorption capability

We report the fabrication of water-stable electrospun polyethyleneimine (PEI)/polyvinyl alcohol (PVA) nanofibers that have super dye sorption capability. Electrospinning parameters including flow rate, applied voltage, and polymer concentration were optimized to obtain smooth and uniform PEI/PVA nanofibers. The nanofibers with a mean diameter of 490 ± 83 nm can be rendered water insoluble via crosslinking using glutaraldehyde vapor. The formed nanofibers with a smooth and uniform morphology before and after crosslinking were characterized using scanning electron microscopy, Fourier transform infrared spectroscopy, and mechanical property testing. The sorption capability of the PEI/PVA nanofibers was confirmed by UV-vis spectrometry. We show that the water-stable nanofibrous mats can effectively absorb methyl blue, which is a typical dye used in the printing and dyeing industry. The dye sorption kinetics and isotherm follow the pseudo-second-order model and the Langmuir model, respectively. The developed polymer nanofiber system has a great potential in decolorizing dyeing wastewater for environmental remediation applications.

Polyelectrolyte multilayer film-assisted formation of zero-valent iron nanoparticles onto polymer nanofibrous mats

A facile approach that combines the electrospinning technique and layer-by-layer (LbL) assembly method has been developed to synthesize and immobilize zero-valent iron nanoparticles (ZVI NPs) onto the surface of nanofibers for potential environmental applications. In this approach, negatively charged cellulose acetate (CA) nanofibers fabricated by electrospinning CA solution were modified with bilayers composed of positively charged poly(diallyl-dimethyl-ammoniumchloride) (PDADMAC) and negatively charged poly(acrylic acid) (PAA) through electrostatic LbL assembly approach to form composite nanofibrous mats. The composite nanofibrous mats were immersed into the ferrous iron solution to allow Fe(II) ions to complex with the free carboxyl groups of PAA, and then ZVI NPs were immobilized onto the composite nanofibrous mats instantly by reducing the ferrous cations. Combined scanning electron microscopy (SEM), transmission electron microscopy (TEM), energy dispersive spectroscopy (EDS), and thermogravimetry analysis demonstrated that the ZVI NPs are successfully synthesized and uniformly distributed into the polyelectrolyte (PE) multilayer films assembled onto the CA nanofibers. The present approach to synthesis ZVI NPs opens a new avenue to fabricating various materials with high surface area for environmental, catalytic, and sensing applications.