Ladder-Structured Polysilsesquioxane/Al<Subscript>2</Subscript>O<Subscript>3</Subscript> Nanocomposites for Transparent Wear-Resistant Windows

As a protective layer for deformable displays, we synthesized ladder-type polysilsesquioxanes (LPSQs) containing cyclic epoxy as a curable unit. The mechanical properties after photo- and thermal-curing of LPSQs with a small amount of added Al₂O₃ nanoparticles were compared with those of the pure LPSQs. The prepared LPSQ-Al₂O₃ nanocomposites and the pure LPSQs exhibited comparable optical transparencies and thermal stabilities. In addition, the degree of conversion of the applied epoxy units in LPSQs and the resulting mechanical properties, as monitored by Fourier transform infrared spectroscopy and nanoindentation tests, indicated that the addition of nanoparticles to LPSQs moderately enhanced the epoxy conversion rate and remarkably improved the wear resistance, including hardness, after photo-/thermal-curing processes. The LPSQ-Al₂O₃ nanocomposites achieved higher wear resistance than epoxy-silica nanocomposites containing similar curable functional groups and reinforcing fillers (silica). The excellent mechanical properties of the LPSQ-Al₂O₃ nanocomposites could be attributed to three-dimensionally interconnected networks of organic-inorganic hybrid-type chemical structures in the LPSQ as well as additional reinforcement from amine-functionalized Al₂O₃ nanoparticles covalently interconnected with the LPSQ. We believe that the devised LPSQ-Al₂O₃ nanocomposites could serve effectively as a wear-resistant platform for deformable display windows.     

Effect of phase transformation on physical and biological properties of PVA/CaFe<Subscript>2</Subscript>O<Subscript>4</Subscript> nanocomposite

The thermal treatment method was employed to achieve higher homogeneity of calcium ferrite (CaFe2O4) and Poly (vinyl alcohol) (PVA) nanocomposites. The influences of phase transformation on physical and biological properties of calcined specimens were investigated by various experimental techniques including X-ray diffraction (XRD), Transmission Electron Microscopy (TEM), high resolution Field emission scanning electron microscope (FESEM) and Fourier transform infrared spectroscopy (FT-IR). Heat treatment was conducted at temperatures between 723 and 923 K, so that a phase transformation occurred from cubic to orthorhombic spinel structure at 923 K. The chemical analysis of the PVA/CaFe₂O₄ nanocomposite was performed by energy dispersion X-ray analysis (EDXA), demonstrated the PVA/CaFe₂O₄ nanocomposites contained the elements of C, Ca, Fe, and O. The formed nanocomposites exhibited ferromagnetic behaviors which were confirmed by using a vibrating sample magnetometer (VSM). The calcined specimens were carried out to an antimicrobial or antifungal test.     

Fabrication and characterization of nano Al<Subscript>2</Subscript>O<Subscript>3</Subscript> filled PVA:NH<Subscript>4</Subscript>SCN electrolyte nanofibers by electrospinning

Present paper reports a method of preparing polymer composite electrolyte nanofiber mat using polyvinyl alcohol (PVA), ammonium thiocynate (NH₄SCN) salt, and aluminium oxide (Al₂O₃) nano particles based on electrospinning technique. Two-stage process of preparation of nanofibers, namely, preparation of nano particles filled PVA electrolyte gel solution followed by its electrospinning has been used. The so obtained nanofibers have been characterized by XRD, DSC, SEM, and Conductivity measurements. XRD patterns affirm the formation of nanocomposite while SEM pictures reveal formation of fibers on a nano scale format (300–800 nm). Fibers of the electrolytes are seen to be thermally stable. Ionic conductivity of electrolyte fiber is seen to improve in the presence of nano filler at room temperature with a maximum at 5.31×10⁻³ Scm⁻¹ for 4 wt% filler concentration, which is comparable to that for corresponding dried gel electrolyte films.     

Controlling the Properties of OPEFB/PLA Polymer Composite by Using Fe<Subscript>2</Subscript>O<Subscript>3</Subscript> for Microwave Applications

Microwave-absorptive polymer composite materials provide protection against interference to communication systems caused by microwave-inducing devices. Microwave-absorptive polymer composites were prepared from polylactic acid (PLA) biocomposite blended with oil palm empty fruit bunch (OPEFB) fiber and commercial Iron oxide (Fe₂O₃) as filler using the melt-blending method. The composites characterization was carried out using the scanning electron microscopy (SEM) and X-ray diffraction (XRD) analyses. The coefficient of reflection S₁₁ and coefficient of transmission S₂₁ of the composites for various Fe₂O₃ filler percentages were determined using a rectangular waveguide in connection with microwave vector network analyser (HP/Agilent model PNA N5227). These coefficients were then used to calculate microwave-absorption properties (in decibels). XRD analysis showed that increasing amounts of reinforced material (Fe₂O₃) reduces the crystallinity of the composites. SEM data indicated that Fe₂O₃ filler ratio increased in the composites, and adhesion to the cellulose fiber grew gradually until the highest percentage of filler was added. The complex relative permittivity and relative permeability were obtained within the broad frequency range of 8–12 GHz at room temperature for various percentages of filler and were measured by the transmission/reflection method using a vector network analyser. Fe₂O₃ embedment in OPEFB/PLA was observed to have resulted in enhancing the dielectric and magnetic properties. The values of permittivity and permeability increased with increasing Fe₂O₃ filler content. Theoretical simulation studied the relation between ε′ and ε″ of the relative complex permittivity in terms of Cole-Cole dispersion law. The result indicated that the processes of Debye relaxation in Fe₂O₃/OPEFB/PLA, the unique dielectric characteristics of Fe₂O₃ cannot be accounted for by both the Debye dipolar relaxation and natural resonance. Results further showed that the material transmission, reflection, and absorption properties could be controlled by changing the percentage of Fe₂O₃ filler in the composites.     

Degradation and kinetic modeling of polyvinyl alcohol in aqueous solutions by a H<Subscript>2</Subscript>O<Subscript>2</Subscript>/Mn(II) system

This paper is about the degradation of polyvinyl alcohol (PVA) in aqueous solutions using a H2O2/Mn(II) system. Fourier transform infrared spectroscopy (FTIR) and gel permeation chromatography (GPC) were applied to analyze the degradation products of PVA, and the results revealed that the backbone chain of PVA could be effectively broken and oxidized. Several unsaturated degradation products, including carboxylic acids, ketones, aldehydes, olefins, and alkynes were also detected and identified by gas chromatography-mass spectrometry (GC-MS), which indicated that higher treatment temperatures would considerably promote the generation of lower molecular weight degradation products. According to the work presented in this paper, the degradation efficiency of PVA increased from 55 % at 60 oC to 99 % at 90 oC after treatment when the initial PVA concentration was 5 %, at pH=3 with a H2O2 and Mn(II) dose of 100 ml/l and 0.6 mol/l, respectively. In addition, kinetic modeling indicated that the experimental results were best fitted by the Page-modified model with an activation energy of 48.78 kJ/mol.     

Preparation and characterization of inner-pressure hollow fiber composite membrane via two-way coating technique for CO<Subscript>2</Subscript>/CH<Subscript>4</Subscript> separation

High-selectivity inner-pressure hollow fiber composite (HFC) membrane for CO₂/CH₄ separation was prepared through the Two-way coating (TWC) technique. The blends of poly(vinylamine) (PVAm)/polyvinyl alcohol (PVA) were coated onto porous hollow fiber polysulfone (PSF) ultrafiltration (UF) membrane with an effective membrane area of 0.4 m². The effects of fabrication parameters on the permselectivity of the resultant HFC membrane were investigated and the optimum preparation conditions were obtained as follows: coating time for 30 min and air blowing time for 30 min after the coating. The prepared HFC membrane showed the typical characteristic of fixed carrier membrane with a high selectivity of CO₂ and CH₄: the separation factor of CO₂/CH₄ (40 vol% CO₂ at 25 °C and 0.2 MPa) was 36.6 and the CO₂ permeability was 56.3 GPU. Field emission scanning electron microscopy (FESEM) images indicated that the HFC membrane prepared by TWC technique had a uniform coating layer along the whole hollow fiber. Membrane permselectivity showed almost no difference between different membrane sections. The HFC membrane showed a good stability during the continuous testing process of 540 h. And the HFC membrane preserved at 30 °C and 40 % humidity exhibited a good durability with a basically unchanged separation factor after 30 days.     

Preparation and UV-protective property of PVAc/ZnO and PVAc/TiO<Subscript>2</Subscript> microcapsules/poly(lactic acid) nanocomposites

The poly(vinyl acetate) (PVAc)/zinc oxide (ZnO) microcapsule and PVAc/titanium dioxide (TiO₂) microcapsule were synthesized via in-situ emulsion polymerization method. The PVAc/ZnO microcapsule and PVAc/TiO₂ microcapsule were characterized by fourier transform infrared spectroscopy (FTIR), thermogravimetric analysis(TG), transmission electron microscopy (TEM), and UV-visible spectroscopy (UV-vis). Effect of PVAc/ZnO microcapsule and PVAc/TiO₂ microcapsule on properties of poly(lactic acid) (PLA) was evaluated by UV-vis, SEM and mechanical properties test. The results showed that the addition of PVAc/ZnO and PVAc/TiO₂ microcapsules as a UV-blocking additive could significantly enhance UV-blocking property of PLA/PVAc/ZnO microcapsule composites and PLA/PVAc/TiO₂ microcapsule composites compared with pure PLA, PLA/ZnO composites and PLA/TiO₂ composites. The mechanical properties of PLA/PVAc/ZnO microcapsule composites were better than those of PLA/ZnO composites due to good dispersability and compatibility of PVAc/ZnO microcapsule in PLA matrix. Also, the mechanical properties of PLA/PVAc/TiO₂ microcapsule composites were better than those of pure PLA and PLA/TiO₂ composites. This study demonstrates the great potentials of the intrinsically UV shield additive PVAc/ZnO and PVAc/TiO₂ microcapsules in the application of high performance matrix resin and composite material.     

Multifunctional modification of wool fabric using graphene/TiO<Subscript>2</Subscript> nanocomposite

In this study, a new finishing technique is introduced through treatment of wool fabric with graphene/TiO₂ nanocomposite. Graphene oxide/titanium dioxide nanocomposite first applied on the wool fabric by hydrolysis of titanium isopropoxide in graphene oxide suspension and then this coating chemically converted by sodium hydrosulfite to graphene/TiO₂ nanocomposite. The homogenous distribution of the graphene/TiO₂ nanocomposite on the fiber surface was confirmed by field emission scanning electron microscopy (FE-SEM), Energy-dispersive X-ray spectroscopy (EDS) and X-ray mapping. X-ray diffraction patterns proved the presence of titanium dioxide nanoparticles with a crystal size of 127 Å on the treated wool fabric. Also, the defect analysis based on X-ray photoelectron spectroscopy (XPS) established the composition of the nanocomposite. Other characteristics of treated fabrics such as antibacterial activity, photo-catalytic self-cleaning, electrical resistivity, ultraviolet (UV) blocking activity and cytotoxicity were also assessed. The treated wool fabrics possess significant antibacterial activity and photo-catalytic self-cleaning property by degradation of methylene blue under sunlight irradiation. Moreover, this process has no negative effect on cytotoxicity of the treated fabric even reduces electrical resistivity and improves UV blocking activity.     

In situ loading TiO<Subscript>2</Subscript> and its photocatalysis and UV resistance on cotton fabric

Anatase TiO₂ nanoparticles was in-situ formed on the cotton fabric by using tetrabutyl titanate (TBT) as a precursor through the normal pressure hydrothermal method. X-ray diffraction (XRD), Scanning electron microscopy (SEM), UV visible spectra (UV-VIS), ATR-IR were used as the characterization techniques. Photocatalytic performance of TiO₂ on the fabric surface was evaluated by methylene blue (MB), 4 kinds of the common living stains and three dyes under ultraviolet and visible light radiation. XRD analysis found that the TiO₂ loaded on the fabric was mainly anatase crystalline phase with particle size of 6.4 nm. SEM observed that a large number of nano TiO₂ particles are distributed on the fabric surface. UV-VIS test indicated that theTiO₂-coated fabric possessed an obvious absorption for ultraviolet. ATR-IR analysis indicated that the nano-TiO₂ possesses a strong affinity with the hydroxyl group of the cotton fabric, and the soaping tests showed that the TiO₂ was firmly bonded with the fabrics. The treated fabrics have good degradation ability for MB aqueous solution, and could degrade azo, anthraquinone and phthalocyanine dyes. The order of degradation of the common life stains was: pepper oil> tea > coffee > soy sauce.     

The effect of floating vegetation on CH<Subscript>4</Subscript> and N<Subscript>2</Subscript>O emissions from subtropical paddy fields in China

Duckweed (Lemna minor), a floating macrophyte belonging to the Lemnaceae family, is commonly found in subtropical paddy fields. This plant rapidly takes up nutrients from water and forms dense floating mats over the water surface that may impact the biogeochemical processes and greenhouse gas production in paddy fields. In this study, we measured CH₄ and N₂O emissions from duckweed and non-duckweed plots in a subtropical paddy field in China during the period of rice growth using static chamber and gas chromatography methods. Our results showed that CH₄ emission rate ranged from 0.19 to 26.50 mg m^?2 h^?1 in the duckweed plots, and from 1.02 to 28.02 mg m^?2 h^?1 in the non-duckweed plots. The CH₄ emission peak occurred about 1 week earlier in the duckweed plots compared to the non-duckweed counterparts. The mean CH₄ emission rate in the duckweed plots (9.28 mg m^?2 h^?1) was significantly lower than that in non-duckweed plots (11.66 mg m^?2 h^?1) (p < 0.05), which might be attributed to the higher water and soil Eh in the former. N₂O emission rates varied between ?50.11 and 201.82 µg m^?2 h^?1, and between ?28.93 and 54.42 µg m^?2 h^?1 in the duckweed and non-duckweed plots, respectively. The average N₂O emission rate was significantly higher in the duckweed plots than in the non-duckweed plots (40.29 vs. 11.93 µg m^?2 h^?1) (p < 0.05). Our results suggest that the presence of duckweed will reduce CH₄ emission, but increase N₂O flux simultaneously. Taking into account the combined global warming potentials of CH₄ and N₂O, we found that growing duckweed could reduce the overall greenhouse effect of subtropical paddy fields by about 17 %.     

Effect of organic,inorganic and slow-release urea fertilisers on CH<Subscript>4</Subscript> and N<Subscript>2</Subscript>O emissions from rice paddy fields

Vietnam is one of the world’s top two rice exporting countries. However, rice cultivation is the primary source of agriculture’s greenhouse gas (GHG) emissions in Vietnam. In particular, strategies are required to reduce GHG emissions associated with the application of organic and inorganic fertilisers. The objective of this study was to assess the effects of various combinations of biochar (BIOC), compost (COMP) and slow-release urea (SRU) on methane (CH₄) and nitrous oxide (N₂O) emissions. In total, 1170 gas samples were collected from closed gas chambers in rice paddies at Thinh Long commune and Rang Dong farm in northern Vietnam between June and October 2014. The gas samples were analysed for CH₄-C and N₂O-N fluxes using gas chromatography. The application of BIOC alone resulted in the lowest CH₄ emissions (4.8–59 mg C m^?2 h^?1) and lowest N₂O emissions (0.15–0.26 µg N m^?2 h^?1). The combined application of nitrogen–phosphorus–potassium (NPK) + COMP emitted the highest CH₄ (14–72 mg C m^?2 h^?1), while ½NPK + BIOC emitted the highest N₂O (1.03 µg N m^?2 h^?1 in the TL commune), but it was the second lowest (0.495 µg N m^?2 h^?1) in the RD farm. Green urea and orange urea reduced N₂O emissions significantly (p < 0.05) compared to white urea, but no significant differences were observed with respect to CH₄ emissions. SRU fertilisers and BIOC alone measured the lowest greenhouse gas intensity, i.e. <2.5 and 3 kg CO₂ eq. kg^?1 rice grain, respectively. Based on these results, application of fertilisers in the form of BIOC and/or orange or green urea could be a viable option to reduce both CH₄ and N₂O emissions from rice paddy soils.     

Performance of PTT fabric treated with CNTs/SiO<Subscript>2</Subscript>/thiazole dye hybrid materials

A series of CNTs/SiO₂/thiazole dye hybrid materials prepared via the sol-gel process is synthesized from carbon nanotubes (CNTs) and tetraethoxysilane with heteroaryl 4-phenyl-2-amino-thiazole dyes. Heterocyclic 4-phenyl-2-aminothiazole dyes are processed with the hydrolysis-condensation reaction at a constant ratio of vinyltriethoxysilane and tetraethoxysilane condensed with modified CNTs in appropriate proportion under a catalyst. The structures of the CNTs/SiO₂/thiazole dye hybrid materials are characterized by Fourier transform infrared spectroscopy (FTIR). Polytrimethylene terephthalate (PTT) fabrics are used to evaluate the morphology structure by scanning electron microscopy (SEM). SEM images show that a uniform dyeing on the PTT fabrics to confirm the reaction of hybrid materials with PTT fabrics. The washing fastness, color evenness, water contact angle, air permeability, electric conductivity, and weatherability of PTT fabrics dyed with CNTs/SiO₂/thiazole dye hybrid materials are evaluated, with results indicating improved conductivity and water-repellent.     

The synergy effect of Graphene/SiO<Subscript>2</Subscript> hybrid materials on reinforcing and toughening epoxy resin

Based on the situ preparation of silica nanoparticles (SiO₂) on the surface of Graphene nanoplatelets (GNPs) in the previous work, these unique three dimensional (3D) materials were introduced into epoxy resin to study the reinforcing and toughening synergy effect on the composites. Firstly, the tensile tests showed that Graphene/SiO₂ hybrid materials attached with different size of SiO₂ particles exhibited different reinforcing and toughening effect on the composites. With the increasing of the diameter of SiO₂ particles, the toughness and strength properties of the composites firstly improved and then decreased, and when the average diameter was 0.14 μm, the elongation reached the max.. Meanwhile, the fractured surfaces presented on SEM images were consistent with the results of the tensile tests, which further explained the hybrid materials increased the interfacial adhesion between the fillers and matrix, leading to significant improvement in mechanical properties. Moreover, the DSC curves demonstrated that Graphene/SiO₂ hybrid materials accelerated the curing process of epoxy resin due to the cross-link structure between fillers and matrix. Lastly, the crack propagation modes were built to clarify the synergy effect mechanism of reinforcing and toughening on nanoparticles/epoxy resin composites.     

Coloration and Decoloration of Textiles Using a TiO<Subscript>2</Subscript> Composite Pigment

A colorable pigment was prepared by dye adsorption onto titanium dioxide and subsequent silane coating. The effects of pH value, dye concentration, and adsorption times on dye adsorption were discussed. Large adsorption capacity of an anionic dye was obtained at pH value of 2 and the adsorption process was well described by the Langmuir isotherm model. Good dyeability and color fastness of pigment dyed fabric were achieved in the normal life cycle under sunlight. The decoloration of pigment was realized through photocatalytic degradation of dye molecules by titanium dioxide under ultraviolet irradiation when reusing the pigment dyed textiles after disposal. The new absorption peaks in the FTIR spectrum at 2924.95 cm^-1, 1714.91 cm^-1, 1461.17 cm^-1, and 1289 cm^-1 verified silane modification. Silane modification improved fixation of dyes onto the pigment and immobilization of pigments onto substrates. The close attachment of silane coating layer to titanium dioxide was conducive to photodegradation of dye molecules in the pigment.     

Evaluating the Mechanical Behavior of Basalt Fibers/Epoxy Composites Containing Surface-modified CaCO<Subscript>3</Subscript> Nanoparticles

Polymer matrix composites (PMCs) owing to their outstanding properties such as high strength, low weight, high thermal stability and chemical resistance are broadly utilized in various industries. In the present work, the influence of silanized CaCO₃ (S-CaCO₃) with 3-aminopropyltrimethoxysilane (3-APTMS) coupling agent at different values (0, 1, 3 and 5 wt.% with respect to the matrix) on the mechanical behavior of basalt fibers (BF)/epoxy composites was examined. BF-reinforced composites were fabricated via hand lay-up technique. Experimental results from three-point bending and tensile tests showed that with the dispersion of 3 wt.% S-CaCO₃, flexural strength, flexural modulus, tensile strength and tensile modulus enhanced by 28 %, 35 %, 20 % and 30 %, respectively. Microscopic examinations revealed that the development of the mechanical properties of fibrous composites with the incorporation of modified CaCO₃ was related to enhancement in the load transfer between the nanocomposite matrix and BF as well as enhanced mechanical properties of the matrix part.     

Modification and Characterization of Nano-TiO<Subscript>2</Subscript> for Efficient Fixation on Cotton Fibers

In this paper, a silane coupling agent, 3-aminopropyltriethoxysilane, was reacted with nano-TiO₂ to introduce amino group onto it which was then reacted with trichlorotriazine to obtain a dichlorotriazine functionalized nano-TiO₂ for the firm fixation of it on cotton fibers. The reaction process was monitored by the titration of primary and secondary amino groups, and the reaction conditions were optimized with orthogonal method accordingly. The dichlorotriazine functionalized nano-TiO₂ was reacted with cotton fabric by the nucleophile substitution reaction to afford nano-TiO₂ functionalized cotton fabric, the structure and surface morphology of the nano-TiO₂ finished cotton fibers were studied by FT-TR and SEM. In addition, the fixation duration of the nano-TiO₂ modified cotton was studied according to AATCC test method 61–2010. The results show that the washing fastness of the nano-TiO₂ is excellent.     

Synthesis of electrospun carbon nanofiber/WO<Subscript>3</Subscript> supported Pt,Pt/Pd and Pt/Ru catalysts for fuel cells

In the present study, nano-sized Pt/WO₃-carbon nanofiber, Pt-Pd/WO₃-carbon nanofiber and Pt-Ru/WO₃-carbon nanofiber electrocatalysts were synthesized and the performance of prepared catalysts were compared with catalysts coated carbon black for the oxygen reduction reaction (ORR). The morphology and structure of prepared catalysts were characterized using scanning electron microscopy (SEM) and X-ray diffraction (XRD) analysis. The SEM images showed that the catalyst nanoparticles were well dispersed on the both carbon nanofiber and carbon black supports. Electrochemical measurements including linear sweep voltammetry (LSV), electrochemical impedance spectroscopy (EIS) and chronoamperometry (CA) tests were applied to investigate the potential of the fabricated electrodes on the ORR. The results demonstrated that the catalysts based on carbon nanofibers showed a significant increase of activity toward the ORR. Also, the Pt/Pd coated carbon nanofibrous electrode showed the highest electrochemical activity.     

Rapid fabrication and optimization of silk fibers supported and stabilized MnO<Subscript>2</Subscript> catalysts

We report on the in situ synthesis and stabilization of manganese dioxide (MnO₂) onto four different silk yarns (mulberry, tasar, muga and eri silks). A new ultrasound-assisted procedure was used to reduce permanganate (MnO₄ ^?) and yielded MnO₂ nanoparticles (NPs) on/in the different silk fibers. Using a factorial design we assessed the influence of the silk type, manganese precursor concentration, sonication time, and temperature. The results indicated no measurable effect of the process parameters on the silk structures, but significant correlation with the rate of degradation of methylene blue (MB) and the fraction of permanganate consumed. Further optimization of the factorial model identified the optimal process conditions for each silks: mulberry (150 min sonication, 20 mM permanganate), eri (360 min, 10 mM), tasar (150 min, 10 mM) and Muga (20 min, 10 mM). The operational stability (successive catalysis) of the optimum hybrids showed good performance over 5 cycles and most importantly reduced direct dye absorption relatively to dye oxidation. Overall, we found that all silks could template the formation and stabilization of different MnO₂ polymorphs and yielded catalytic instead of stoichiometric hybrid fibers.     

Immobilization of Cationic Titanium Dioxide (TiO<Subscript>2</Subscript><Superscript>+</Superscript>) on Electrospun Nanofibrous Mat: Synthesis,Characterization, and Potential Environmental Application

We report a facile approach to fabrication and characterization of cationic titanium dioxide (TiO₂⁺) on poly (vinyl alcohol)/poly (acrylic acid) (PVA/PAA) composite electro-spun nanofibrous mat. The aim of this study is to develop a “functional electrospun nanofibrous mat” as a sustainable approach to superior photocatalytic degradation of organic colorants. For that, the PVA/PAA nanofibrous mat was prepared by electrospinning of PVA and PAA solution according to an aspect ratio of 1:1 and later water stability was induced by the thermal cross linking at an elevated temperature of 145 °C for 30 minute. By means of electrostatic layer-by-layer (LbL) assembly, cationic titanium dioxide (TiO₂⁺, ~19 nm) was immobilized on the surface of the water stable nanofibrous mat. As functionalized composited nanofibrous mat was characterized by using scanning electron microscope (SEM), fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD) analysis and thermogravimetric analysis (TGA). Superior competency of the functionalized nanofibrous mat towards photocatalytic degradation of organic dye (methyl blue) in aqueous solution was observed by using UV-visible spectrophotometer with quantitative measuring method. The result indicates a complete degradation of methyl blue within 40 mins and superior reusability upto 5 cycles application. The study signifies the prospect of using electrospun nanofibers to manipulate the catalytic activity, which could be a foundation for further rational design of various composite nanofibrous materials.     

Development of UV Protective,Superhydrophobic and Antibacterial Textiles Using ZnO and TiO<Subscript>2</Subscript> Nanoparticles

In this research work, multifunctional cotton fabric comprising of UV protection, superhydrophobicity and antibacterial activity has been developed using facile pad-dry-cure method. In the first step, the concentration of repellent chemical has been optimized. Then, formulations containing nanoparticles of ZnO or TiO₂ along with optimized concentration of repellent chemical and organic-inorganic binder have been applied to cotton fabric followed by the evaluation of functional properties. The surface morphology and elemental composition of treated fabric has been characterized through SEM and EDX, respectively. The treated samples have shown promising UV protection, superhydrophobicity and antibacterial properties durable upto 20 washing cycles.