Effectiveness of PANI/Cu/TiO2 ternary nanocomposite on antibacterial and antistatic behaviors in polyurethane coatings

Surfaces with antibacterial and antistatic functionalities are one of the new demands of todays' industry. Therefore, a facile method for the preparation of multifunctional polyaniline/copper/TiO₂ (PANI/Cu/TiO₂) ternary nanocomposite based on in situ polymerization is presented. This nanocomposite was characterized through the different techniques and was utilized for induction of antibacterial and antistatic properties in polyurethane coatings. Measurement of the conductivity of PANI/Cu/TiO₂ ternary nanocomposite indicated higher electrical conductivity of this nanocomposite compared to pure PANI. The antibacterial activity of the modified polyurethane coatings was tested against Gram-positive and Gram-negative bacteria which led to remarkable reduction in bacterial growth. Besides, it was observed that polyurethane coating with 2 wt % content of ternary nanocomposite has a surface electrical resistance equal 4 × 10⁸ Ω/sq which acquires surface electrical resistance of standard antistatic coatings. The final coatings were also characterized in terms of thermal and mechanical properties to investigate the effect of the ternary nanocomposite on improvement of these properties. © 2020 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137, 48825.     

Effects of nanosilica and titanium oxide on the performance of epoxy–amine nanocoatings

Different types of composite coatings were prepared by the blending of colloidal nanosilica (SiO₂) and titanium dioxide (TiO₂) in epoxy resin to investigate their coating performances. A fixed amount of silica nanoparticles (20 wt %) and different amounts (5, 10, and 15 wt %) of microsized TiO₂ particles were used in the coatings. The functional groups of the formulated coatings were confirmed by Fourier transform infrared spectroscopy. These results indicate that the SiO₂–TiO₂ particles interacted well with epoxy. Scanning electron microscopy images of the composite coatings revealed a good dispersion of TiO₂ particles at a lower amount of loading; this improved the adhesiveness, glass-transition temperature, thermal stability, and chemical resistance properties. At higher loadings, the performances decreased. The composite coatings were also characterized by their UV radiation-absorption properties with an ultraviolet–visible spectrophotometer. Interestingly, this property was found to be enhanced at higher loadings. An impressive result was noticed in the nanocomposites in terms of oxygen transmission rate performance compared to that of the neat epoxy. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47901.     

Multifunctionality of poly(vinyl alcohol) nanofiber webs containing titanium dioxide

We prepared titanium dioxide/PVA nanocomposite fiber webs for application in multifunctional textiles by electrospinning. The morphological properties of the TiO₂/PVA nanocomposite fibers were characterized using scanning electron microscopy and transmission electron microscopy. Layered fabric systems with electrospun TiO₂ nanocomposite fiber webs were developed using various concentrations of TiO₂ and a range of web area densities, and then the UV‐protective properties, antibacterial functions, formaldehyde decomposition ability, and ammonia deodorization efficiency of the fabric systems were assessed. Layered fabric systems with TiO₂ nanocomposite fiber webs containing 2 wt% TiO₂ nanoparticles at 3.0 g m^?2 web area density exhibited an ultraviolet protection factor of greater than 50, indicating excellent UV protection. The same system showed a 99.3% reduction in Staphylococcus aureus. Layered fabric systems with TiO₂ nanocomposite fiber webs containing 3 wt % TiO₂ nanoparticles at 3.0 g m^?2 web area density exhibited a 85.3% reduction in Klebsiella pneumoniae. Titanium dioxide nanocomposite fiber webs containing 3 wt % TiO₂ nanoparticles at 3.0 g m^?2 web area density exhibited a formaldehyde decomposition efficiency of 40% after 2 h, 60% after 4 h, and 80% after 15 h under UV irradiation. The same system showed an ammonia deodorization efficiency of 32.2% under UV irradiation for 2 h. These results demonstrate that TiO₂ nanocomposite fibers can be used to produce advanced textile materials with multifunctional properties. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Corrosion resistance and photocatalytic activity evaluation of electrophoretically deposited TiO2-rGO nanocomposite on 316L stainless steel substrate

TiO₂-rGO nanocomposite coatings were obtained by electrophoretic deposition (EPD) technique of TiO₂ nanoparticles and graphene oxide (GO) on stainless steel substrate. First, GO particles were synthesized using a modified Hummers' method. GO was reduced electrochemically to form a coating in the presence of nano-sized TiO₂ particles. The influences of different parameters such as GO concentration, coupling co-electro-deposition parameters (electrophoretic duration and voltage) on thickness, surface morphology and, corrosion behavior of the as-synthesized TiO₂-rGO nanocomposite coatings were systematically surveyed. The morphology and microstructure were investigated by field emission scanning electron microscopy (FE-SEM), Raman spectra and X-ray diffraction (XRD) techniques. Atomic force microscopy (AFM) was harnessed to evaluate the topography of the as-prepared GO powder. The bonding characteristics of as-synthesized and as-reduced GO were examined after deposition, by Energy Dispersive Analysis of X-Ray (EDX) and Fourier-transform infrared spectroscopy (FT-IR). Corrosion behavior of coatings and that of the pure TiO₂ layer were evaluated by electrochemical impedance spectroscopy (EIS) and polarization techniques (by applying potentiodynamic polarization spectroscopy (PDS)). Detailed SEM studies showed that increasing EPD voltage brings about a coating with increased porosity and microcracks with higher thickness. In addition to that, the presence of rGO reduced corrosion current density (i_corr) and shifted corrosion potential (E_corr) toward more noble values in 3.5% NaCl at room temperature. Also, Analyses revealed that the optimum electrophoretically synthesized coating was obtained at GO concentration of 1 g/L, 30 V and 30 min at room temperature. The corrosion current density of the corresponding coating was remediated up to 0.2 μA cm⁻², which means an anti-corrosion ability of about 30 times compared to TiO₂-coated and bare 316L stainless steel. The results of impedance spectroscopic studies demonstrated that this coating renders as a barrier layer and resistance increased from 2.95 KΩ cm² for TiO₂-coated layer to 10.49 KΩ cm² for the optimized layer.     

Hybridizing MWCNT with nano metal oxides and TiO2 in epoxy composites: Influence on mechanical and thermal performances

In this study, the effects of multi‐walled carbon nanotubes (MWCNT), and its hybrids with iron oxide (Fe₂O₃) and copper oxide (CuO) nanoparticles on mechanical characteristics and thermal properties of epoxy binder was evaluated. Furthermore, simultaneous effects of using MWCNT with TiO₂ as pigment and CaCO₃ as filler for epoxy composites were determined. To investigate effects of nano‐ and micro‐particles on epoxy matrix, the samples were evaluated by TGA and DTA. It was found that the hybrid of MWCNT with nano metal oxides caused considerable increment in the tensile and flexural properties of epoxy samples in comparison to the single MWCNT containing samples at the same filler contents. Significant improvement in the thermal conductivity of epoxy samples was obtained by using TiO₂ pigment along with MWCNT. The TiO₂ pigment also caused considerable improvement in mechanical properties of the epoxy matrix and the MWCNT containing nanocomposite. The best mechanical and thermal properties of epoxy nanocomposites were obtained at 1.5 wt % of MWCNT and 7 wt % of TiO₂ that it should be attributed to particle network forming of the particles which cause better nano/micro dispersion and properties. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43834.     

Sol–gel preparation and characterization of antibacterial and self-cleaning hybrid nanocomposite coatings

ZnO–TiO₂, SiO₂–TiO₂, and SiO₂–TiO₂–ZnO hybrid nanocomposite coatings were synthesized based on sol–gel precursors including tetramethoxysilane (TMOS), 3-glycidoxypropyl trimethoxysilane (GPTMS), tetra(n-butyl orthotitanate) (TBT), and zinc acetate dihydrate. The hybrid network was characterized by FTIR, FESEM, and EDAX techniques. Results indicated that inorganic particles’ size was of nanoorder (20–30 nm), with very uniform distribution and dispersion. Photocatalytic and self-cleaning activities of these coatings were further investigated by degradation of methylene blue in an aqueous solution (20 ppm) at visible light irradiation, indicating photocatalytic performance of the coatings containing ZnO and TiO₂ nanoparticles. The antibacterial effect of the coatings was investigated for inhibition and inactivation of cell growth, with the results showing the same antibacterial activity for ZnO–TiO₂ and SiO₂–TiO₂–ZnO coatings against Escherichia coli and Staphylococcus aureus; the activity was, however, higher than that of SiO₂–TiO₂ hybrid nanocomposite coatings.     

Preparation of epoxy resin/CaCO3 nanocomposites and performance of resultant powder coatings

Epoxy resin/CaCO₃ nanocomposites were prepared by the methods of extruding, solution blending, and in situ and inclusion polymerization, respectively. The contents of nanoparticles in the nanocomposites were varied from 5 wt % to 15 wt %. Powder coatings with different content of nanoparticles were made from the nanocomposites. The results showed that the cupping property and impact resistance decreased with the increase of coating film thickness. The dispersion of nanoparticles in epoxy matrix affected the impact resistance and cupping property of the obtained coating films greatly. The coating films made from the nanocomposite prepared by in situ and inclusion polymerization showed that the best impact resistance and the maximum cupping property was achieved when nano‐CaCO₃ content was 5 wt %. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 101: 2656–2660, 2006     

Incorporation of ZnO–ZrO2 nanoparticles into TiO2 coatings obtained by PEO on Ti–6Al–4V substrate and evaluation of its corrosion behavior,microstructural and antibacterial effects exposed to SBF solution

In this research, Plasma Electrolytic Oxidation technique was used to incorporate ZnO–ZrO₂ nanoparticles into TiO₂ ceramic coating on Ti6–Al–4V using sodium phosphate as an electrolyte. The effect of adding these nanoparticles on corrosion, morphology, wettability and antibacterial properties in the simulated body fluid (SBF) solution was investigated. The results indicated nanoparticles modified the microstructure of coating, which increased corrosion resistance 12 times higher than that of substrate. Besides, ZrO₂ nanoparticles had the most significant effect on increasing the contact angle. In addition, due to the compatibility of zirconium and zinc oxides with human body environment, the antibacterial properties of coatings were significantly improved.     

Efficient preparation of hybrid nanocomposite coatings based on poly(vinyl alcohol) and silane coupling agent modified TiO2 nanoparticles

In the present investigation, at first, the surface of titanium dioxide (TiO₂) nanoparticles was modified with γ-aminopropyltriethoxy silane as a coupling agent. Then a new kind of poly(vinyl alcohol)/titanium dioxide (PVA/TiO₂) nanocomposites coating with different modified TiO₂ loading were prepared under ultrasonic irradiation process. Finally, these nanocomposites coating were used for fabrication of PVA/TiO₂ films via solution casting method. The resulting nanocomposites were fully characterized by Fourier transform infrared spectroscopy (FT-IR), powder X-ray diffraction (XRD), thermogravimetric analysis/derivative thermal gravimetric (TGA/DTG), transmission electron microscopy (TEM), scanning electron microscopy (SEM) and atomic force microscopy (AFM). The TEM and SEM results indicated that the surface modified nanoparticles were dispersed homogeneously in PVA matrix on nanoscale and based on obtained results a possible mechanism was proposed for ultrasonic induced nanocomposite fabrication. TGA confirmed that the heat stability of the nanocomposite was improved. UV–vis spectroscopy was employed to evaluate the absorbance and transmittance behavior of the PVA/TiO₂ nanocomposite films in the wavelength range of 200–800 nm. The results showed that this type of films could be used as a coating to shield against UV light.     

Hydrophobic composite coatings with photocatalytic self-cleaning properties by micro/nanoparticles mixed with fluorocarbon resin

A newly developed hydrophobic composite coating was fabricated by incorporating modified TiO₂ nanoparticles and hydrophobic material polytetrafluoroethylene (PTFE) micropowders dispersed in fluorocarbon resin. Moreover, the surface characteristics and self-cleaning properties of the newly developed composite material were examined. The material was found to exhibit sufficient hydrophobicity with a water contact angle of 133°. The surface free energy of the composite coating was 4.11 mJ/m². Scanning electron microscopy results revealed a micro/nanocomposite structure composed of PTFE micropowders and TiO₂ nanoparticles, which was verified by X-ray photoelectron spectroscopy results. Through ultraviolet irradiation the modified TiO₂-PTFE/FEVE composite coating successfully removed oleic acid absorbed on its surface. These results showed that the functional composite coating had a sufficiently hydrophobic surface with an efficient self-cleaning effect.     

Phase inversion process to prepare quasi-solid-state electrolyte for the dye-sensitized solar cells

A quasi-solid-state electrolyte for the dye-sensitized solar cells was prepared following the phase inversion process. The microporous polymer electrolyte based on poly(vinylidene fluoride-co-hexafluoropropylene) (P(VDF-HFP)) hybrid with different amount of TiO₂ nanoparticles were prepared. The surface morphologies, the differential scanning calorimetry, and the ionic conductivity of the microporous polymer electrolyte were tested and analyzed. The results indicated that the microporous polymer electrolyte with TiO₂ nanoparticles modification exhibited better ionic conductivity compared with the original P(VDF-HFP) polymer electrolyte. The optimal ionic conductivity of 0.8 mS cm⁻¹ is obtained with the 30 wt % TiO₂ nanoparticles modification. When assembled with the 30 wt % TiO₂ nanoparticles modified quasi-solid-state electrolyte, the dye-sensitized TiO₂ nanocrystalline solar cell exhibited the light to electricity conversion efficiency of 2.465% at light intensity of 42.6 mW cm⁻², much better than the performance of original P(VDF-HFP) microporous polymer electrolyte DSSC. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Melt-spinning and thermal stability behavior of TiO<Subscript>2</Subscript> nanoparticle/polypropylene nanocomposite fibers

The elongational flow properties of TiO₂ nanoparticle/polypropylene (PP) nanocomposite fibers were studied via melt spinning. The diameter, tension, and flow rate of fibers were directly measured and used to calculate the apparent elongational viscosity and apparent elongational strain rate using Cogswell’s theory. Thermal gravimetric analysis (TGA) was used to demonstrate that the TiO₂ nanoparticles improved the thermal stability of the PP fibers. With a 1–3 wt % loading of the TiO₂ nanoparticles, the PP fiber decomposition temperatures ranged from 338 °C for the pristine polymer to 342, 349, and 367 °C; the decomposition was accompamied by an initial 95 wt % weight loss. In addition, the well-distributed morphology of the TiO₂ nanoparticles on the side surface of the PP matrix was observed using atomic force microscopy (AFM). At 1 wt % loading of the TiO₂ nanoparticles, the surfaces of the PP nanofibers contained mono-disperse nanoparticles with sizes of 20–50 nm. Furthermore, the TiO₂ nanoparticle/PP nanocomposite fibers were shown to be thermally stable and are suitable for application as an antibacterial polymer.     

Extended hydrophobicity and self-cleaning performance of waterborne PDMS/TiO<Subscript>2</Subscript> nanocomposite coatings under accelerated laboratory and outdoor exposure testing

It has been shown that incorporation of TiO₂ nanoparticles into hydrophobic coatings can show self-cleaning performance. Accelerated laboratory testing indicated that the coats retain their hydrophobic nature for an extended time period. In this paper, hydrophobic polydimethylsiloxane (PDMS)/TiO₂ nanocomposite coatings with a TiO₂ content of 0–40% were fabricated by simple blending of a PDMS dispersion with an aqueous TiO₂ nanoparticle dispersion. Their long-term hydrophobicity and self-cleaning performance were investigated both in laboratory and real-world outdoor testing. As expected, TiO₂ nanoparticle-based coatings exhibited better self-cleaning relative to the TiO₂-free PDMS control coating as measured by methylene blue degradation testing. Excellent long-term hydrophobicity was observed in accelerated weathering testing when they contained the appropriate levels of TiO₂ nanoparticles (i.e., 0–30%). However, the same PDMS/TiO₂ coatings did not show self-cleaning performance, and instead, exhibited improved dirt pickup resistance, in outdoor exposure testing. Sustained hydrophobicity was observed in outdoor exposure testing for the clear films except when TiO₂ levels were at 40%. The hysteresis of water contact angle (HWCA) significantly increased for the PDMS control coating, and water beading was lost as the film surface picked up dirt. In contrast, the TiO₂-based coatings with appropriate TiO₂ levels maintained a relatively low HWCA after outdoor exposure and no water sheeting on rainy days was observed. This result demonstrates that while photocatalytic TiO₂ nanoparticles can maintain coating hydrophobicity upon outdoor exposure, long-term self-cleaning performance in polluted environments has not yet been achieved with this type of coating under real-world conditions.     

Composite ceramic coating with enhanced thermal shock resistance formed by the in-situ synthesis of nano-ZrO2

In this research, nano-ZrO₂/TiO₂ composite coatings were designed for titanium alloys by the in-situ incorporation of ZrO₂ nanoparticles into a TiO₂ ceramic coating. Precise control over the content and structure of nano-ZrO₂ in this nanocomposite coating was achieved by manipulating the pH of the electrolyte during plasma electrolytic oxidation (PEO). The synthesis process and mechanism of tetragonal zirconia (t-ZrO₂) were revealed by analyzing the phase composition and microstructure of the coating. The influence of pH on the formation of t-ZrO₂ was also revealed. By detecting changes in the electrolyte solute composition before and after PEO, the Zr(OH)₄ precursor was determined to be the source of the t-ZrO₂ nanoparticles in the composite coating. The yield of t-ZrO₂ in the composite coating increased upon increasing the pH of the electrolyte. Moreover, the thermal shock tests showed that increasing the t-ZrO₂ content remarkably improved the thermal resistance of the coatings. This strategy and the research outcomes are expected to have great significance for developing advanced nanocomposite coatings on titanium alloys with enhanced thermal shock resistance.     

SiAlON–epoxy nanocomposite coatings: Corrosion and wear behavior

In this study, epoxy powder as a matrix was combined with different contents of silicon–aluminum–oxygen–nitrogen (SiAlON) nanoparticles using a planetary ball mill. Pure epoxy and nanocomposite powders were applied on the surface of plain carbon steel components by the electrostatic spraying method. Curing of the coatings was done in an oven or microwave for the appropriate time. The coating structure and morphology of the SiAlON nanoparticles were studied by scanning electron microscopy and transmission electron microscopy, respectively. The corrosion properties of the coatings were assessed by immersion, Tafel polarization, and electrochemical impedance spectroscopy tests in 3.5% NaCl solution. The results show that addition of 10 wt % SiAlON nanoparticles markedly increases the corrosion resistance of epoxy coatings. Thus, it can be inferred that the corrosion rate of these coatings is 15 to 18 times lower than that of pure epoxy samples and 8 to 11 times lower than coatings with 20 wt % SiAlON. The higher corrosion resistance of nanocomposite coatings can be attributed to the barrier properties of SiAlON nanoparticles. The tribological performance of the coatings was studied with the pin‐on‐disk test. The results of wear testing show that the samples containing 10 wt % SiAlON provide about five times more wear resistance than pure ones and about two times more than coatings with 20 wt % SiAlON. However, the coefficient of friction for nanocomposite coatings is reduced about 50% compared to the pure sample. Also, the curing process in either regime (oven or microwave) has the same effect on the corrosion and wear properties, and the coatings are completely crosslinked. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43855.     

Development of Poly(aniline-co-o-toluidine)/TiO2 nanocomposite coatings for low carbon steel corrosion in 3.5% NaCl solution

Chemical oxidative polymerization of aniline (AN) and o-toluidine (OT) for the synthesis of copolymer, Poly(AN-co-OT) and its composite with TiO₂ nanoparticles, Poly(AN-co-OT)/TiO₂ employing ammonium persulfate as an oxidant and HCl as an external dopant were carried out. The homopolymers, Polyaniline and Poly(o-toluidine) were also prepared by following similar method. The synthesized polymers were characterized with FTIR spectroscopy, XRD/SEM/TEM analysis. The anticorrosive coatings were synthesized in dimethyl sulfoxide solution by dissolving synthesized polymers, and then were applied on low-carbon steel (LCS) samples using epoxy binder. The anticorrosive potential of the polymer coatings containing copolymer, copolymer-nanocomposite and homopolymers on LCS was evaluated in 3.5% NaCl at a temperature of 30?°C by open circuit potential, electrochemical impedance spectroscopy and potentiodynamic polarization measurements. It was observed that the nanocomposite coating increases the protection efficacy by providing better barrier properties against corrosion as compared with neat copolymer and homopolymers coatings. The morphology of the coatings before and after 60 days LCS immersion in 3.5% NaCl solution was determined using SEM.     

TiO2–ZnO/Ni–5wt.%Al composite coatings on GH4169 superalloys by atmospheric plasma spray techniques and theirs elevated-temperature tribological behavior

Ni–based composite coatings with different amounts of TiO₂–ZnO were fabricated by atmospheric plasma spraying (APS) to protect GH4169 superalloy substrates against excess wear and friction at elevated temperatures. In addition, the influence of the simultaneous addition of the oxides on the microstructure, microhardness, and wear behaviour was investigated. According to the results, the simultaneous addition of TiO₂/ZnO provides anti-friction and wear inhibition over 600 °C. In particular at 800 °C, the TiO₂–ZnO/Ni–5wt.%Al composite coating (10 wt% TiO₂ and 10 wt% ZnO were incorporated within Ni–5wt.%Al matrix) exhibits a superior lubricity and wear resistance compared to the Ni–5wt.%Al based coatings. The XRD, Raman, and TEM characterisations reveal the formation of a glaze oxide layer consisting of NiO, TiO₂, ZnO and the in-situ production of ternary oxide (Zn₂TiO₄), which was primarily responsible for the tribological performance of the sliding wear contacts at the specific temperature.     

Modeling and optimization of a new impact-toughened epoxy nanocomposite using response surface methodology

This paper reports the development of a high-impact epoxy nanocomposite toughened by the combination of poly(acrylonitrile-co-butadiene-co-styrene) (ABS) as thermoplastic, clay as layered nanofiller, and nano-TiO₂ as particulate nanofiller. Response surface methodology (RSM) was applied for optimization and modeling of the impact strength of epoxy/ABS/clay/TiO₂ quaternary nanocomposite. A second-order mathematical model between the response (impact strength) and variables (ABS, clay and nano-TiO₂ contents) was derived. Analysis of variance (ANOVA) showed a high coefficient of determination value (R ² = 98%). Under optimum conditions, maximum impact strength of 29.2 KJ/m² with 197% increase compared to neat epoxy was experimentally obtained. Also correlation between morphology and impact strength of the nanocomposite was investigated using scanning electron microscopy (SEM) and X-ray diffraction (XRD). A dispersion of exfoliated clay platelets, TiO₂ nanoparticles with low agglomeration and ABS nanoparticles was obtained as morphology of the nanocomposite. A new and more effective method for impact toughening of epoxy was introduced. This study clearly showed that the addition of the combination of layered and particulate nanofillers along with ABS as thermoplastic has a considerable enhancement effect on impact strength of epoxy.     

TiO2-graphene nanocomposite for electrochemical sensing of adenine and guanine

TiO₂-graphene nanocomposite was prepared by hydrolysis of titanium isopropoxide in colloidal suspension of graphene oxide and in situ hydrothermal treatment. It provides an efficient and facile approach to yield nanocomposite with TiO₂ nanoparticles uniformly embedded on graphene substrate. The electrochemical behavior of adenine and guanine at the TiO₂-graphene nanocomposite modified glassy carbon electrode was investigated. The results show that the incorporation of TiO₂ nanoparticles with graphene significantly improved the electrocatalytic activity and voltammetric response towards these species comparing with that at the graphene film. The TiO₂-graphene based electrochemical sensor exhibits wide linear range of 0.5–200 μM with detection limit of 0.10 and 0.15 μM for adenine and guanine detection, respectively. The excellent performance of this electrochemical sensor can be attributed to the high adsorptivity and conductivity of TiO₂-graphene nanocomposite, which provides an efficient microenvironment for electrochemical reaction of these purine bases.     

Effect of addition of nanosized UV absorbers on the physico-mechanical and thermal properties of an exterior waterborne stain for wood

This study describes the effects of the addition of inorganic nanosized UV absorbers on physico-mechanical and thermal properties of an exterior commercial acrylic-based waterborne stain for wood. Electronic microscopy and water vapor (WV) permeability measurements were performed to characterize the free films of the acrylic stain and resulting nanocomposite coatings. An accelerated weathering method was used to evaluate aging behavior of the coatings on wood through appearance, T_g, abrasion resistance, adhesion strength, hardness and Young's modulus changes. In addition to improving the protection against UV, the doped TiO₂ and silica-coated ZnO nanoparticles in powder form have improved the abrasion resistance and barrier effect against water vapor diffusion of the acrylic stain. For most of nanocomposite coatings, the addition of ZnO hydrophilic nanoparticles in predispersed form has resulted in a decrease in WV permeability, while the adhesion strength and abrasion resistance of those coatings were negatively affected. The addition of ZnO nanoparticles has decreased the T_g of the acrylic stain. Finally, the accelerated weathering has induced an increase in T_g, hardness, Young's modulus (stiffness) and an increase in apparent adhesion strength and abrasion resistance of the coatings. The T_g values of the aged nanocomposite coatings were lower than that of unmodified acrylic stain.