Surface modification of fabrics is a powerful strategy that can endow fabrics with desired effects while keeping the intrinsic properties. Herein, an ordinary strategy, dipping-drying based layer-by-layer self-assembly (LbL) coating, is reported to functionalize fabrics’ surfaces. Firstly, the novel cation waterborne polyurethanes (QAHDPU) and anion waterborne polyurethanes (HDPU) are successfully designed and synthesized. By incorporating targeted molecule, hydantoin diol (HD) and quaternary ammonium salt with long alkyl chain (DOQA), the QAHDPU are antibacterial and hydrophobically functionalized. Taking advantage of strong adhesion, waterborne polyurethanes (WPUs) are physically bonded to surfaces of fabrics to generate durable antibacterial and hydrophobic fabrics. The QAHDPU with long alkyl chain combined with rough and porous fabric surface fabricates hydrophobic fabric surface, which can prevent bacteria from adhering to the fabrics. Furthermore, the coated fabrics present excellent antibacterial properties after chlorination, forming a second barrier against bacteria. The chlorinated coated fabrics, can inactivate 85.0–99.9% of Staphylococcus aureus and 85.0–97.7% of Escherichia coli with contact time of 60 min. The hydrophobic properties of coated fabrics are greatly improved with water contact angles of 122.0°–141.1°. In addition, the proposed method is applicable for a variety of fibers and expected to be used for industrial production.
We report here the use of a layer-by-layer assembly technique to prepare novel TiO2 heterogeneous nanostructures in which anatase nanoparticles are assembled on rutile nanorods. The preparation includes assembling anatase nanoparticle multilayers on rutile nanorods via electrostatic deposition using poly(sodium 4-styrene sulfonate) as a bridging or adhesion layer, followed by burning off the polymeric material via calcination. The composition of the heterogeneous nanostructures (i.e., the anatase-to-rutile ratio) can be tuned conveniently by controlling the experimental conditions of the layer-by-layer assembly. It was found that, with the optimum preparation conditions, the heterogeneous nanostructures showed better photocatalytic activity for decomposing gaseous acetaldehyde than either the original anatase nanoparticles or the rutile nanorods. This is discussed on the basis of the synergistic effect of the existence of both rutile and anatase in the heterogeneous nanostructure. 相似文献
The possibility of in situ photoreduction of Ag+-ions using TiO2 nanoparticles deposited on cotton and cotton/PET fabrics in the presence of amino acid alanine and methyl alcohol has been discussed. The possible interaction between TiO2, alanine and Ag+-ions was evaluated by FTIR analysis. The fabrication of TiO2/Ag nanoparticles on both fabrics was confirmed by SEM, EDX, XRD, XPS and AAS analyses. Cotton and cotton/PET fabrics impregnated with TiO2/Ag nanoparticles provided maximum reduction of Gram-negative bacteria Escherichiacoli and Gram-positive bacteria Staphylococcusaureus. Although excellent antibacterial activity was preserved after ten washing cycles, a significant amount of silver leached out from the fabrics into the washing bath. The perspiration fastness assessment revealed that smaller amounts of silver were also released from the fabrics into artificial sweat at pH 5.50 and 8.00. In addition, deposited TiO2/Ag nanoparticles imparted maximum UV protection to fabrics. 相似文献
We report on the synthesis of ZnO and TiO2 nanoparticles by solution-phase methods, with a particular focus on the influence of experimental parameters on the kinetics
of nucleation and coarsening. The nucleation rate of ZnO from the reaction between ZnCl2 and NaOH in ethanol was found to increase with increasing precursor concentration, while the coarsening rate is independent
of precursor concentration up to a threshold concentration. The nucleation rate of ZnO from Zn(OOC-CH3)2 and NaOH in n-alkanols was found to decrease with decreasing chain length, which is explained by the increase of the dielectric
constant of the solvent. Due to the larger solubility of ZnO, nucleation is significantly slower than that observed in the
case of TiO2. TiO2 nanoparticles coarsen according to the Lifshitz-Slyozov-Wagner model for Ostwald ripening. We also show that using amorphous
titania as a base material, pure anatase and brookite nanoparticles can be synthesized. 相似文献
Highly crystalline, near monodisperse TiO2 nanoparticles, nanorods and their metal-ion-doped (Sn4+, Fe3+, Co2+, and Ni2+, etc.) derivatives have been prepared by well-controlled solvothermal reactions. Through adjusting the reaction parameters, such as reaction temperature, duration, and concentration of the reactants, the size, shape, and dispersibility of the products can be controlled. A possible reaction mechanism can be proposed based on experimental evidence. 相似文献
In this article, we report on the chemical oxidative polymerization of 3-methylthiophene (3MTh) in a concentrated TiO2/CHCl3 homogeneous suspension with an oxidant/monomer mole ratio of 3 at room temperature. According to the scanning electron microscopy images, in this condition, poly(3-methylthiophene) (P3MTh) was prepared with fibrous morphology decorated by nano-dimensional TiO2 particles. P3MTh/TiO2 was also characterized by Fourier transform infrared spectroscopy and X-ray diffraction techniques. It was found that no aggregation of nanoparticles occurred during the polymerization process. In addition, the thermal stability of P3MTh/TiO2 nanocomposite was investigated by thermogravimetric analysis and compared with that of an analogously prepared neat P3MTh. The thermal degradation of P3MTh in the temperature range of 300–550°C decreases significantly due to the presence of the TiO2 nanoparticles in the polymer composite. 相似文献
Photocatalytic TiO2 nanoparticles are effective photocatalyzers which can damage the cellular membranes and genetic supramolecules such as DNA. In this experiment, we observed the lesion efficacy of the photocatalytic TiO2 nanoparticles upon the cellular membrane and genetic molecule by transmission electron microscopy and single cell gel electrophoresis assay, and the mechanisim of the cell death by photocatalytic TiO2 nanoparticles. 相似文献
The effect of the nanostructure on the photochemistry of TiO2 is an active field of research owing to its applications in photocatalysis and photovoltaics. Despite this interest, little is known of the structure of small particles of this oxide with sizes at the nanometer length scale. Here we present a computational study that locates the global minima in the potential energy surface of Ti(n)O2n clusters with n = 1-15. The search procedure does not refer to any of the known TiO2 polymorphs, and is based on a novel combination of simulated annealing and Monte Carlo basin hopping simulations, together with genetic algorithm techniques, with the energy calculated by means of an interatomic potential. The application of several different methods increases our confidence of having located the global minimum. The stable structures are then refined by means of density functional theory calculations. The results from the two techniques are similar, although the methods based on interatomic potentials are unable to describe some subtle effects. The agreement is especially good for the larger particles, with n = 9-15. For these sizes the structures are compact, with a preference for a central octahedron and a surrounding layer of 4- and 5-fold coordinated Ti atoms, although there seems to be some energy penalty for particles containing the 5-fold coordinated metal atoms with square base pyramid geometry and dangling Ti=O bonds. The novel structures reported provide the basis for further computational studies of the effect of nanostructure on adsorption, photochemistry, and nucleation of this material. 相似文献
The decomposition of silver selenide and sulfide to metallic silver and chalcogen containing oxygen compounds by sintering with an equimolar mixture of sodium nitrate and nitrite was examined. It was found that 100% recovery of silver in a metal phase is reached at 5% excess of sodium nitrate and nitrite and a time of the isothermal exposure at 375 °C for 1 hour or 0.5 hours at 400°C. 相似文献
Anatase TiO2 nanoparticles with a size range of 2 to 10 nm have been formed on carbon nanotubes by the controlled hydrolysis and condensation of titanium bis-ammonium lactato dihydroxide in water and electrosterically dispersed carbon nanotubes. 相似文献
A simple self-catalyzed hydroamination method for creating hybrid TiO(2)-polyaniline core-shell nanoparticles (NP) has been shown. Hybrid NPs with a range of possible sizes are afforded in high yield under mild reaction conditions and simultaneously show improved charge transport and electrochromic behavior compared to either polyaniline alone or physically blended with TiO(2). 相似文献
Chemical grafting of anti-oxidant molecules with an additional hydrophobic polymer coating directly onto TiO(2) particle surfaces, using sonochemistry, is found to eliminate photocatalytic degradation enabling highly effective screening against UV radiation. 相似文献
Au particles (mean size ca. 3 nm) supported on TiO(2) particles were irradiated by UV light (>300 nm) in aqueous solutions at 278 K. Photo-induced dissolution of Au nanoparticles followed by redeposition occurred in aqueous solutions containing halogen ions. The dissolution of Au nanoparticles yielded a Au(III) complex with a halogen ion; subsequent reduction of the Au(III) complex caused precipitation of larger Au particles on TiO(2). 相似文献
Titanium dioxide nanoparticles can be produced by the controlled hydrolysis of titanium tetraisopropoxide in water-in-CO2 (w/c) microemulsions stabilized with the surfactants ammonium carboxylate perfluoropolyether (PFPE-NH4) and poly(dimethyl amino ethyl methacrylate-block-1H,1H,2H,2H-perfluorooctyl methacrylate) (PDMAEMA-b-PFOMA); the greater control of hydrolysis and particle growth with PDMAEMA-b-PFOMA is consistent with the differences in the stabilities and interactions for these two microemulsions. 相似文献
In this study, very small (2–5 nm) TiO2 nanoparticles were synthesized in an aprotic solvent, N,N-dimethylacetamide, via hydrolysis and condensation of titanium alkoxide at room temperature. The synthesized TiO2 sol showed 30 days of storage stability and could be used to prepare high-refractive-index TiO2-polyimide hybrid thin films by an ex-situ method that involved a spin coating and multistep baking process. The field emission scanning electron microscope image showed a flat and uniform morphology of the hybrid thin film. TiO2 domains were in the nanometer range, thus avoiding light scattering. The refractive index at 633 nm of the hybrid thin film reached 2.05, which suggested potential applications of the film to anti-reflective coatings and optical waveguides. 相似文献