Soap‐free emulsion copolymerization of perfluoroalkyl acrylates in the presence of a reactive surfactant

Soap‐free emulsion copolymerization of perfluoroalkyl acrylate (FA)/methyl methacrylate (MMA)/n‐butyl acrylate (n‐BA) was carried out in the presence of sodium 2‐acrylamide‐2‐methyl propanesulfonate (AMPSNa) as a reactive surfactant and potassium persulfate (KPS) as an initiator. An analysis of the effects of concentration of AMPSNa, KPS, FA as well as polymerization temperature on the kinetic features (rate of polymerization) and colloidal characteristics (mean particle diameter, particle disperse index, particle numbers, and surface charge density) was followed. NMR, FTIR, AFM, and fluorine‐selective electrode analysis were used to characterize the composition and morphology of the FA copolymers. Both AFM analysis and contact angle measurements strongly implied that the fluorinated segments migrated to the outmost surface and created films with lower surface energy. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 104: 2438–2444, 2007     

Synthesis and characterization of crosslinking waterborne fluorinated polyurethane‐acrylate with core‐shell structure

Crosslinking core‐shell emulsions of waterborne fluorinated polyurethane‐acrylate (WFPUA) were successfully synthesized using a solvent‐free method. The crosslinkers of diacetone acrylamide and adipic dihydrazide were introduced into the WFPUA emulsions. The physical properties of hybrid emulsions such as the average particle size, stability, and viscosity were characterized. The core‐shell of crosslinking WFPUA emulsion synthesized in this study was observed by transmission electron microscopy. Then, the results of Fourier transform infrared spectroscopy, atomic force microscopy, and X‐ray photoelectron spectroscopy indicated that the fluorinated monomer (FA) had been polymerized into the crosslinking waterborne polyurethane‐acrylate polymer, and the fluorinated groups have evident enrichment on the film‐air surface with the increase of FA content. At the same time, the thermal properties, water repellent/antifouling properties, and mechanical properties were measured. Moreover, the thermal properties and the elongation are raised but tensile stress and shore hardness are decreased with the increase of FA content. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40970.     

Preparation and properties of poly(siloxane‐ether‐urethane)‐acrylic hybrid emulsions

Poly(siloxane‐ether‐urethane)‐acrylic (PU‐AC) hybrid emulsions were prepared by introducing different hydroxyethoxypropyl‐terminated polydimethylsiloxane (PDMS) content into the acrylic‐terminated poly(ether‐urethane) backbone and then in situ copolymerizing with methyl methacrylate and butyl acrylate via emulsion process. The effects of PDMS on the particle size and viscoelastic behavior of the hybrid emulsions were investigated. Meanwhile, the hydrogen bonding, mechanical and thermal mechanical properties, water resistance, the surface gloss, and wettability of the resultant hybrid films were also studied. The results showed that all the hybrid emulsions showed shear‐thinning behaviors, and the introduction of PDMS resulted in the formation of the hybrid emulsions with increased average particle size and decreased viscosity. The chemical bonds built between PU and AC yielded higher than 73% crosslinking fraction in all the hybrid materials, but this value decreased with increasing PDMS content because PDMS reduced the hydrogen bonding interactions and enhanced the phase separation. As a result, an increase in the PDMS content led to an increase in the elongation, water resistance, surface roughness, and water hydrophobic of the films, but the tensile strength, hardness, storage modulus, and glass transitions temperature decreased. It is suggested that introduction of PDMS can provide the hybrid materials with the improved flexibility, water resistance, and surface hydrophobicity, which has potential application value in the fouling‐release coatings, biomaterials, and surface fishing. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 44927.     

Considerations of functional fluoropolymer structure in the design of acrylic–fluorine hybrid PSAs: Graft versus telechelic cooligomers

The objectives of this present article are to design and compare novel acrylic‐fluorine networks as the replacement of fluorinated polyacylate for adhesives application. Firstly, two effective strategies have been developed to achieve functional poly(VDF‐co‐HFP) copolymers based on commercial fluoropolymers. The first approach extensively involved the facile chemical degradation of commercial poly(VDF‐co‐HFP) copolymers to obtain telechelic cooligomers. The second route dealt with the preparation of functional fluoropolymers grafted by multiplex acrylate. Then these two functional and original products were applied as precursors of acrylic‐fluorine hybrid networks in situ polymerization with acrylic monomers. In contrast to original fluoropolymers, functional poly(VDF‐co‐HFP) copolymers exhibited better compatibility with acrylic chain, especially after crosslinking by aluminium acetylacetonate. Additionally, the surface properties of acrylic‐fluorine hybrid networks were discussed based on the SEM and contact angle test. Finally, the peel strength and shear holding power measurements indicated that acrylic‐fluorine hybrid networks can find their potential applications in low surface energy fluorinated PSAs. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 46038.     

Effect of hydrophilic monomer on the surface properties of cationic polyurethane‐fluorinated acrylate hybrid dispersions

Cationic polyurethane‐fluorinated acrylate hybrid dispersions (PUFA) were prepared by the copolymerization of styrene, butyl acrylate, and 2,2,3,4,4,4‐hexafluorobutyl methacrylate in the medium of crosslinked polyurethane via phase inversion polymerization. The said polyurethane was synthesized in acetone from 2,4‐tolyene diisocyanate, N‐methyldiethanolamine, trimethylolpropane, and soft polyester diol block. The influences of hydrophilic monomer on the surface properties, immersion behaviors, particle size and, zeta potential of the dispersions were investigated. The results show that the addition of hydrophilic monomer can be advantaged to the stability of dispersions and yet will increase the surface free energy by more than 19.9%. The PUFA coating films cured at ambient conditions have the lower surface free energy (less than 0.02033 J/m²). At the same time, there is an obvious mobility of fluorinated groups in fluorinated polymer films. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci, 2006     

含氟乳化剂丙烯酸酯乳液的制备及性能

以丙烯酸丁酯、甲基丙烯酸甲酯、丙烯酸、十二烷基硫酸钠为主要成份分别制备了含氟乳化剂FC80、FC91 1、FC90 8、4 FC氟醇的丙烯酸酯共聚物乳液 ,测定了它们的表面张力、粘度、PH值、固含量等性能 ,重点讨论了 FC80含量对乳液性能的影响。实验发现在 FC80含量为 0 .0 5%时丙烯酸酯共聚物乳液性能变化明显     

Preparation of porous polymer materials using water‐in‐oil gel emulsions as templates

Water‐in‐oil gel emulsions consisting of water and n‐butyl acrylate were successfully prepared using N‐3‐hydroxybutylcarbonyl‐l ‐isoleucylaminooctadecane and sorbitan monooleate (Span 80) as gelator and surfactant, respectively. Stable gel emulsions were formed using aqueous phase fractions (APFs) ranging from 10 to 90 vol%. Creaming, flocculation and coalescence were not observed. Low‐temperature polymerization of the gel emulsions with a redox initiator gave the corresponding low‐density, highly porous poly(n‐butyl acrylate)s (PBAs). The microstructures of the PBAs were observed using scanning electron microscopy. All the porous PBAs comprised numerous spherical structures whose sizes could be controlled by adjusting the gel emulsion APF. The densities and porosities of the porous PBAs decreased and increased, respectively, with increasing APF. The absorption capacities of the porous PBAs in organic solvents were studied. The porous PBAs selectively absorbed kerosene from water instantly and the kerosene could then be recovered by physical compression of the PBAs. Further porous polymers were prepared from gel emulsions containing styrene, methyl methacrylate (MMA) or 2‐ethylhexyl acrylate (EHA) as continuous oil phases. The order of absorption capacity and swelling ratio in kerosene was poly(EHA) > PBA ? poly(MMA). Porous copolymers were also prepared from gel emulsions containing a mixture of EHA and MMA as the oil phase. Their absorption and swelling in liquids could be controlled by changing the ratio of EHA and MMA in the gel emulsions. poly(EHA‐co‐MMA) (6:4) was the best polymer when absorption capacity, swelling ratio and durability were simultaneously considered. © 2018 Society of Chemical Industry     

Polyurethane‐acrylic hybrid emulsions with high acrylic/polyurethane ratios: Synthesis,characterization, and properties

Allyl polyoxyethylene ether (APEE) was used as coupling agent between polyurethane (PU) and acrylic polymer (AC) to synthesize stable waterborne polyurethane‐acrylic (PU‐AC) hybrid emulsions with high AC/PU weight ratio ranged from 45/55 to 70/30. The effect of the AC/PU weight ratio and the acrylate type including methyl methacrylate (MMA), butyl acrylate (BA) and mixture of them on the properties of the synthesized emulsions and resultant films were investigated. The research results showed that the colloidal particle of the emulsions behaved core‐shell structure, and the copolymers were not crosslinked. An increase in the AC/PU weight ratio led to an increase in the average particles size and the particle size distribution, but decrease in the viscosity of the emulsions. Meanwhile, the molecular weight distribution of the copolymers became wide, and the tensile stress, shore A hardness, storage modulus, glass transfer temperature, water resistance, and water contact angle of the resultant films increased, except that the films of PU‐BA were too soft to determine their mechanical properties. MMA and BA can provide the PU‐AC hybrid emulsions with very different properties, and which can be adjusted according to the special application. It was suggested that APEE can not only built up chemical bonds between PU and AC, but also increase the self‐emulsifying ability in the emulsion polymerization due to its hydrophilic ethylene oxide and carboxylic groups, resulting in that PU‐AC hybrid emulsions with high AC/PU ratio can be obtained by this method. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 44488.     

Preparation of fluorescent pigment latex and its application on binder‐free printing of cotton fabrics

The recognized disadvantages of pigment printing are the stiff hand feel owing to the large particle size of the binder and pigments and the crosslinked binder introducing rigidity. In the current study, fluorescent pigment latex (FPL) was prepared via mini‐emulsion polymerization and further applied on cotton fabric printing in the absence of binder. The mini‐emulsions were prepared by dispersing the fluorescein in the monomers methyl methacrylate (MMA) and butyl acrylate (BA) with DNS‐86 as emulsifier, hexadecane as co‐emulsifier, and ammonium persulfate as initiator. The Fourier‐transform infrared‐attenuated total refraction, transmission electron microscopy, differential scanning calorimetry, and thermogravimetric analysis showed that the fluorescein was successfully encapsulated into P(MMA‐co‐BA) and the polymer content was 91.22%. The surface morphology study revealed that compact and smooth film was formed onto the surface of FPL printings, which resulted in better hand feel and rubbing fastness as compared to the conventional printings with a large amount of binder. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 45826.     

Synthesis and properties of novel soluble polyamides containing both fluorene or xanthene cardo moieties and fluorinated phenoxy pendant groups

A series of novel aromatic polyamides containing both fluorene or xanthene cardo moieties and fluorinated phenoxy pendant groups were synthesized from two fluorinated isophthaloyl chlorides and four diamines containing cardo groups by the low‐temperature solution polycondensation in N,N‐dimethylacetamide (DMAc). The obtained polymers were characterized by different physicochemical techniques. All the polymers were amorphous and readily soluble in many organic solvents such as DMAc, N‐methyl‐2‐pyrrolidinone, N,N‐dimethylformamide, dimethyl sulfoxide, pyridine, and tetrahydrofuran at room temperature. The new fluorinated polyamides had high thermal stability with the glass transition temperatures of 237–259°C, the temperatures at 5% weight loss of 437–476°C in nitrogen. All the polymers formed transparent, strong, and flexible films with tensile strengths of 70.6–87.5 MPa, tensile moduli of 2.23–2.78 GPa, and elongations at break of 5.8–8.7%. These polyamide films had high optical transparency with an ultraviolet–visible absorption cutoff wavelength of 352–368 nm, low dielectric constants of 3.24–3.45 (1 MHz), and lower water absorptions of 1.06–1.43%. POLYM. ENG. SCI., 57:1234–1241, 2017. © 2017 Society of Plastics Engineers     

Preparation and performance of waterborne UV‐curable polyurethane containing long fluorinated side chains

Novel waterborne UV‐curable polyurethane containing long fluorinated side chains (WUVFPU) was prepared and the fluorinated component was incorporated by two novel fluorinated macromolecular diols (FDO) with different chain length as chain extender. FDO was synthesized via free radical polymerization of hexafluorobutyl methacrylate (HFBMA) using 1‐thioglycerol (TG) as chain transfer agent. Extremely low dosage of FDO incorporated could change the surface property significantly. The influence of both the content and chain length of FDO on the surface energy, surface composition and morphology were investigated by contact angle measurement, XPS and AFM. Surface energy significantly decreased at extremely low concentration of FDO. The hydrophobicity was enhanced with increasing both the content and the chain length of FDO. XPS and AFM results revealed the enhancing hydrophobicity was attributed to the enrichment of F atoms and rougher surface morphology. Gel content, pencil hardness, adhesion, and optical transmittance tests were employed to investigate the coating properties of the UV‐cured films. The preparation and investigation of WUVFPU might provide better understanding of the influence of fluorinated chain length on the properties of polyurethane for theory. Moreover, it might provide a facile and effective route to prepare polyurethane materials with low surface energy for engineering and industry. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 44506.     

Preparation and properties of core–shell nanosilica/poly(methyl methacrylate–butyl acrylate–2,2,2‐trifluoroethyl methacrylate) latex

A core–shell nanosilica (nano‐SiO₂)/fluorinated acrylic copolymer latex, where nano‐SiO₂ served as the core and a copolymer of butyl acrylate, methyl methacrylate, and 2,2,2‐trifluoroethyl methacrylate (TFEMA) served as the shell, was synthesized in this study by seed emulsion polymerization. The compatibility between the core and shell was enhanced by the introduction of vinyl trimethoxysilane on the surface of nano‐SiO₂. The morphology and particle size of the nano‐SiO₂/poly(methyl methacrylate–butyl acrylate–2,2,2‐trifluoroethyl methacrylate) [P(MMA–BA–TFEMA)] core–shell latex were characterized by transmission electron microscopy. The properties and surface energy of films formed by the nano‐SiO₂/P(MMA–BA–TFEMA) latex were analyzed by Fourier transform infrared spectroscopy, differential scanning calorimetry, thermogravimetric analysis, scanning electron microscopy/energy‐dispersive X‐ray spectroscopy, and static contact angle measurement. The analyzed results indicate that the nano‐SiO₂/P(MMA–BA–TFEMA) latex presented uniform spherical core–shell particles about 45 nm in diameter. Favorable characteristics in the latex film and the lowest surface energy were obtained with 30 wt % TFEMA; this was due to the optimal migration of fluorine to the surface during film formation. The mechanical properties of the films were significantly improved by 1.0–1.5 wt % modified nano‐SiO₂. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Polymerized high internal‐phase emulsions: Properties and interaction with water

The synthesis and characterization of novel polymerized high internal‐phase emulsions (polyHIPE) materials are described. Homogeneous, highly porous, low‐density, open‐cell crosslinked copolymers were prepared by polymerizing the continuous phase of HIPE containing styrene and varying amounts of 2‐ethylhexyl methacrylate. The glass transition temperatures (T_gs) of the homopolymers were similar to the literature values, but the copolymer T_gs were lower than expected. These results indicate that the copolymer composition is richer in 2‐ethylhexyl methacrylate than the feed composition. The homopolymer moduli, calculated from the foam moduli, were similar to the literature values. The influence of composition and surface treatment on the water absorbed by the foams was investigated. For example, washing a polyHIPE based on poly(ethylhexyl acrylate) in water at 70°C increased water absorption because of the removal of the residual salt. Adding a fluorinated comonomer to the HIPE reduced hydrophilicity and, thus, water absorption. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 84: 2018–2027, 2002; DOI 10.1002/app.10555     

Effects of polymeric emulsifiers on the properties of acrylic emulsion pressure‐sensitive adhesives

A series of polymeric emulsifiers was polymerized with 2‐ethylhexyl acrylate, butyl acrylate, and acrylic acid. The polymeric emulsifiers were used to make emulsion copolymers of 2‐ethylhexyl acrylate, butyl acrylate, and acrylic acid. The average particle size of the synthesized emulsions was around 145 nm and the size distribution was very narrow. Also, the emulsions showed good freeze–thaw stability and adhesion properties. The peel strength and holding power of the emulsions were investigated by changing the composition and molecular weight of the polymeric emulsifier. The results show that the peel strength exhibits a maximum at particular molecular weight and acrylic acid content of the polymeric emulsifier, while the holding power increases with molecular weight. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 94: 1456–1460, 2004     

The effect of nonionic monomer HAM on properties of cationic surfactant‐free acrylic/alkyd hybrid emulsion

A series of cationic acrylic/alkyd resin (CPAAR) hybrid emulsions was successfully prepared through surfactant‐free emulsion polymerization, using methacryloxyethyltrimethyl ammonium chloride, methyl methacrylate, butyl acrylate and alkyd resin as reaction monomers. And nonionic N‐hydroxymethyl acrylamide (HAM) of different content was simultaneously incorporated into the CPAAR backbone. The structure of CPAAR copolymer was characterized by Fourier transform infared spectrometer, and then the effect of HAM content on properties of CPAAR emulsions was studied by particle size analyzer, transmission electron microscopy and rheometer. In addition, thermal properties, water absorption and contact angle of CPAAR latex films were also investigated. The results showed that the CPAAR emulsions prepared with 4.9 wt % HAM displayed smallest average particle size of 92.2 nm. As HAM content increased from 0 to 19.6 wt %, the initial viscosity of the emulsions increased from 22.48 to 53 mPa.s. At the same time, the emulsions transferred from Newtonian fluid to pseudoplastic fluid, and a transition from viscous liquid to elastic liquid was also detected. Meanwhile, the degradation temperature at 5% weight loss increased by 30.59°C. In addition, with increasing HAM content from 0 to 4.9 wt %, the water absorption and surface free energy of films increased by 4.42% and 5.02 mJ m^?2, respectively. However, the water absorption and surface free energy kept almost invariable with further increase in HAM content. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41406.     

Synthesis of graft copolymers from a linear polyolefin through a combination of coordination polymerization and atom transfer radical polymerization

This article reports on a facile route for the preparation of methyl acrylate and methyl methacrylate graft copolymers via a combination of catalytic olefin copolymerization and atom transfer radical polymerization (ATRP). The chemistry first involved a transforming process from ethylene/allylbenzene copolymers to a polyolefin multifunctional macroinitiator with pendant sulfonyl chloride groups. The key to the success of the graft copolymerization was ascribed to a fast exchange rate between the dormant species and active radical species by optimization of the various experimental parameters. Polyolefin‐g‐poly(methyl methacrylate) and polyolefin‐g‐poly(methyl acrylate) graft copolymers with controlled architecture and various graft lengths were, thus, successfully prepared under dilute ATRP conditions. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Synthesis and properties of novel fluoroalkyl end‐capped oligomers containing silsesquioxane segments

Fluoroalkyl end‐capped homo‐ and co‐ oligomers containing silsesquioxane segments were prepared by the reactions of fluoroalkanoyl peroxides with the corresponding methacrylate monomer‐bearing silsesquioxane unit (Si‐MMA) and comonomers such as N,N‐dimethylacrylamide (DMAA) and acrylic acid (ACA). These new fluorinated Si‐MMA oligomers were easily soluble in various organic solvents and were able to reduce the surface tension of m‐xylene effectively. The modified poly(methyl methacrylate) [PMMA] and glass surface treated with fluorinated Si‐MMA homo‐oligomers exhibited a strong oleophobicity, although these fluorinated oligomers possess high oleophilic silsesquioxane segments. In contrast, the modified PMMA surface treated with fluorinated Si‐MMA–DMAA cooligomers exhibited a good hydrophilicity with a strong oleophobicity. In a series of fluorinated Si‐MMA oligomers, fluorinated Si‐MMA homo‐oligomers had a relatively high thermal stability. Therefore, these fluoroalkyl end‐capped Si‐MMA oligomers are suggested to have high potential for new functional materials through their unique properties such as a high solubility and surface active properties. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 86: 3486–3493, 2002     

Synthesis of Bis(1H, 1H, 2H, 2H‐perfluoro‐octyl)methylenesuccinate copolymers and their application on cotton fabrics

Bis(1H, 1H, 2H, 2H‐perfluoro‐octyl)methylenesuccinate (FOM)/ethyl acrylate (EA)/methyl methacrylate (MMA) copolymer (FOME) latexes, FOM/butyl acrylate (BA)/MMA copolymer (FOMB) latexes, and FOM/octyl acrylate (OA)/MMA copolymer (FOMO) latexes were synthesized by continuous emulsion polymerization. Solution polymerization was also carried out to prepare FOMB. The influences of fluorine content and curing conditions on the surface properties of polymer films were discussed. The water and oil repellency of cotton fabrics treated with the FOM copolymers was better than that of conventional poly(fluoroalkyl acrylate)s containing the same fluorinated chain. The polymer films or the treated fabrics were characterized by Fourier transform infrared, scanning electron microscope, atomic force microscopy, thermogravimetric analysis, x‐ray photoelectron spectrometry, and wide angle x‐ray diffraction. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci, 2013     

Synthesis and characterization of core‐shell particles containing a perfluoroacrylate copolymer rich in the shell

A simple synthetic method for preparing the core‐shell latex particles containing fluorinated shell was presented. Polymerization was achieved by a low‐sheer monomer‐starved emulsion polymerization process, thus facilitating mobility and subsequent polymerization of perfluoroacrylate (FA) along with methyl methacrylate (MMA) and n‐butyl acrylate (nBA) monomers. The structure and thermal behavior of the resulting perfluoroacrylate copolymer were investigated by FTIR, NMR, and DSC. Furthermore, PCS, TEM as well as SFM, were carried out to characterize the surface morphology of the particles. These studies illustrated that the incorporation of FA into MMA/nBA particle morphologies facilitated surface phase separation during coalescence, resulted in F‐containing film‐air interfaces. Thus, surface properties with a significant increase in the contact angles could be produced. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2007     

Synthesis and characterization of a novel silicone containing vinylic macromonomer and its uses in the preparation of poly (silicone‐co‐styrene‐co‐butylacrylate) with montmorillonite nanocomposite emulsion

A new silicone containing macromonomer, 4‐(methacrylamido) phenoxy polymethylhydrosiloxane (4‐MPMHS) with a vinyl group, was successfully synthesized. Then poly (silicone‐co‐styrene‐co‐butylacrylate) with montmorillonite, P (Si‐co‐St‐co‐BA) with MMT nanocomposite emulsion was prepared by in situ intercalative emulsion polymerization of styrene (St), butyl acrylate (BA), and 4‐MPMHS, in the presence of organic modified montmorillonite (OMMT) with different OMMT contents (0, 0.5, 1.0, 1.5, and 2 wt %). Potassium persulphate (KPS) was used as an initiator and sodium lauryl sulfoacetate (SLSA) and nonyl phenol ethylene oxide—40 U (NP‐40) were used as anionic and nonionic emulsifiers, respectively. The resulting macromonomer was characterized by elemental analysis, Fourier transformer infrared (FT‐IR), proton (¹H NMR), and carbon (¹³C NMR) nuclear magnetic resonance spectroscopes. The OMMT was characterized by FT‐IR and X‐ray diffraction (XRD). The nanocomposite emulsions were characterized by using Fourier Transform infrared spectroscopy (FT‐IR), laser light scattering, and surface tension method. Thermal properties of the copolymers were studied using thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC) and then the effects of OMMT percent on the water absorption ratio and drying speed were examined. Results showed that OMMT could improve the properties of emulsion. In other words, the properties of nanocomposite emulsions were better when compared with those of the silicone‐acrylate emulsion. The property of nanocomposite emulsion containing 1 wt % OMMT was the best one, and the following advantages were obtained: smaller particle size, faster drying speed, smaller surface tension, and improved water resistance by the incorporation of OMMT. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011