Superhydrophobic and oleophilic micro‐nano hierarchical Pd‐decorated SiO2 layers

This paper reports a novel fluorinated micro‐nano hierarchical Pd‐decorated SiO₂ structure (hereafter called Pd/SiO₂), which was formed by the deposition of Pd nanoparticles (NPs) on SiO₂ microspheres. The SiO₂ layers with microscale roughness were fabricated by electrospraying a solution prepared using the sol‐gel process. Subsequently, the Pd NPs were deposited using an ultraviolet reduction process. The resulting surfaces exhibited a micro‐nano hierarchical morphology. After fluorination, the micro‐nano hierarchical surface exhibited outstanding water repellency with a water contact angle (WCA) of 170° and a sliding angle <5°, indicating excellent superhydrophobic properties. The layers exhibited good long‐term durability and excellent ultraviolet resistance. Interestingly, the surface was oleophilic (CA of oil ~10°). These results show the potential of employing superhydrophobic fluorinated Pd/SiO₂ layers in smart devices, such as self‐cleanable surfaces and intelligent water/oil separation systems.     

Patterning ZrO2 films surface: Superhydrophilic and superhydrophobic properties

A photosensitive sol-gel method was used to pattern the surface of ZrO₂ film with a groove or a processus mastoideus structure. The surface roughness enhanced by the pattern structure had a strong effect on the ZrO₂ film wettability. Compared to an un-patterned ZrO₂ film, the patterned film showed a smaller static water contact angle (CA) and exhibited superhydrophilicity. Interestingly, the patterned ZrO₂ film did not require the use of UV irradiation to induce the superhydrophilicity and exhibited an excellent anti-fogging behavior. The surface modification with a 1H,1H,2H,2H-perfluorooctyltrichlorosilane (PFOTCS) layer was found to induce the change in the wettability of the patterned ZrO₂ films from superhydrophilicity to hydrophobicity/superhydrophobicity. The PFOTCS-modified ZrO₂ film patterned with the processus mastoideus surface resulted in the highest CA value of 155° and the sliding angle (SA) value of about 7°, and almost did not change under UV irradiation or after being annealed below 350 °C. The surface patterning by using a photosensitive sol-gel method was proved to be a practical approach to fabricate the ZrO₂ film with superhydrophilic/superhydrophobic properties.     

The effect of side chains on the reactive rate and surface wettability of pentablock copolymers by ATRP

The reactive rate and surface wettability of three pentablock copolymers PDMS‐b‐(PMMA‐b‐PR)₂ (R = 3FMA, 12FMA, and MPS) obtained via ATRP for coatings are discussed. Poly(dimethylsiloxane) (PDMS) is used as difunctional macroinitiator, poly(methyl methacrylate) (PMMA) as the middle block, while poly(trifluoroethyl methacrylate) (P3FMA), poly(dodecafluoroheptyl methacrylate) (P12FMA) and poly(3‐(trimethoxysilyl)propyl methacrylate) (PMPS) as the end block, respectively. Their reactive rates obtained by gas chromatography (GC) analysis indicate that 3FMA gains 8.053 × 10^?5 s^?1 reactive rate and 75% conversion, higher than 12FMA (4.417 × 10^?5 s^?1, 35%), but MPS has 1.9389 × 10^?4 s^?1 reactive rate and 96% conversion. The wettability of pentablock copolymer films is characterized by water contact angles (WCA) and hexadecane contact angles (HCA). The PDMS‐b‐(PMMA‐b‐P12FMA)₂ film behaves much higher advancing and receding WAC (120° and 116°) and HCA (60° and 56°) than PDMS‐b‐(PMMA‐b‐P3FMA)₂ film (110° and 106° for WAC, 38° and 32° for HAC) because of its fluorine‐rich surface (20.9 wt % F). However, PDMS‐b‐(PMMA‐b‐PMPS)₂ film obtains 8° hysteretic contact angle in WAC (114°–106°) and HAC (32°–24°) due to its higher surface roughness (138 nm). Therefore, the fluorine‐rich and higher roughness surface could produce the lower water and oil wettability, but silicon‐rich surface will produce lower water wettability. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40209.     

Preparation of a new superhydrophobic nanofiber film by electrospinning polystyrene mixed with ester modified silicone oil

A new superhydrophobic nanofiber membrane with certain mechanical strength was prepared by electrospinning the polystyrene (PS) with ester modified silicone oil (EMSO). To increase the roughness and tensile strength, the EMSO with low energy as hydrophobic macromolecular substance was added into PS precursor solution. Then during the process of electrospinning, some of the ester modified silicone oil was distribution on the surface of substrate (PS) fiber films to generate double structure which leaded to the superhydrophobicity. We probed into the relationship between the surface wettability, morphologies, mechanical property, and the mass ratios of ester modified silicone oil /PS, and with the increasing of EMSO, the water CA value increased from 135 ± 0.5° to 152 ± 0.2°and the tensile strength grown from 0.23 MPa to 0.92 MPa. The film shows a network structure consisting of numerous randomly oriented fibers, the diameters of which changed from 0.5 μm to 2.0 μm belong to relatively big diameter fibers, which has great significance to the research of superhydrophobic membrane with big diameter fibers and also this method is easy, convenient and environment friendly. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40718.     

Influence of Deposition Temperature of GDC Interlayer Deposited by RF Magnetron Sputtering on Anode‐Supported SOFC

Gadolinia‐doped ceria (GDC) film, as a barrier layer to prevent chemical reaction between yttria‐stabilized zirconia (YSZ) electrolyte and Ba_0.5Sr_0.5Co_0.8Fe_0.2O_3–δ (BSCF)–GDC cathode, is deposited by radio frequency (RF) magnetron sputtering on YSZ electrolyte, and the influence of deposition temperature on Ni–YSZ/YSZ/GDC/BSCF–GDC single cell performance is investigated. The SEM results show that the GDC film deposited at 30 °C exhibits a porous structure, whereas the GDC film deposited at 400 °C has a dense structure. The single cells show excellent performance when the deposition temperature is above 250 °C, whereas the single cells show poor performance when the deposition temperature is below 200 °C. The large difference in cell performance occurs from their large difference in polarization resistance. The porous structure of GDC interlayer, which cannot well prevent the reaction between BSCF and YSZ, is responsible for the poor performance of the cells with GDC interlayer deposited at a temperature below 200 °C.     

Oleophilic modification of poly(vinyl alcohol) films by functionalized soybean oil triglycerides

In this study, maleinized (SOMAP) and isocyanated soybean oil (SONCO) triglycerides have been successfully grafted onto one surface of poly(vinyl alcohol)(PVA) films to give films that are hydrophilic on one side and hydrophobic on the other. The surface grafting was accomplished by the reaction of succinic anhydride or isocyanate functionalities of soybean oil derivatives and the hydroxyl groups of PVA films. The reaction was run in toluene, using PVA films on glass slides so that only one side of the film was accessible. After grafting, the films were rinsed with hot toluene to remove ungrafted triglycerides from the surface. The reaction on the surface was confirmed by ATR‐FTIR and ¹H‐NMR spectroscopic techniques. A series of films were prepared at different concentrations of SOMAP or SONCO in toluene. The increase in hydrophobicity with an increase in SOMAP or SONCO concentrations was observed by water contact angle measurements. The contact angles on the grafted side of the film reach their maximum value of 88° and 94° for 26 and 2.5% SOMAP and SONCO concentrations in toluene, respectively, while the ungrafted side gives contact angle of 48°. Surface morphologies of PVA‐g‐SOMAP and PVA‐g‐SONCO films were investigated by atomic force microscopy, whereas optical microscopy and staining was used to determine the homogeneity of the films. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Soybean Oil-Based Polyurethane Networks: Shape-Memory Effects and Surface Morphologies

Vegetable oil‐based shape‐memory polyurethane networks are an emerging class of bio‐based functional materials with great potential applications. In this study, a series of different structural soybean oil polyols were synthesized, and utilized to fabricate polyurethane networks by reacting with 1,6‐diisocyanatohexane. The soybean oil‐based polyurethanes (SOPUs) were characterized with differential scanning calorimetry (DSC), dynamic mechanical tests (DMA), tensile testing, shape‐memory testing, and atomic force microscopy (AFM). It was found that SOPUs with a preserved triglyceride structure were fixed in a temporary shape at ?20 °C, while others were fixed in temporary shapes at 4 °C. Although the recovery speeds were different, all the samples could completely regain their permanent shapes at 37 °C (human body temperature). Furthermore, different SOPUs exhibited different surface structures, which might provide the materials with additional values.     

Effect of solvent on surface wettability of electrospun polyphosphazene nanofibers

Two kinds of biodegradable polymers, poly(ε‐caprolactone) (PCL) and poly[(alanino ethyl ester)_0.67 (glycino ethyl ester)_0.33 phosphazene] (PAGP), were electrospun by using four different solvents. All PCL nanofibrous mats had similar surface water contact angles independent of solvents. However, it was found that the water contact angles of PAGP nanofibrous mats were 102.2° ± 2.3°, 113.5° ± 2.2°, 115.8° ± 1.4°, and 119.1° ± 0.7°, respectively, when trifluoroethanol, chloroform, dichloromethane, and tetrahydrofuran were used as a solvent. This difference was supposed mainly due to phosphorous and nitrous atoms in PAGP being dragged to fiber surface with solvent evaporation during the solidification of nanofibers, because of the strong interaction between positive phosphorous atoms and electronegative atoms in solvents. This interaction was confirmed by Fourier Transform Infrared, and the accumulation of phosphorous and nitrous atoms in the solvent‐casting PAGP film surface was identified by X‐ray photoelectron spectrometry analysis. PCL samples did not show the solvent‐controlled surface wettability because it contained fewer polar atoms. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Optimization of amphiphobic structural surface thickness in relation to its functionality on stainless steel plates

Fluorine‐based amphiphobic coatings have been widely used in commercial textiles to provide water‐ and oil‐repelling abilities. However, few reports from the literature survey have discussed the surface structural effects of the coated substrate on amphiphobicity. In this research, various thickness amphiphobic coatings based on mixed epoxy, tetraethylorthosilicate, and a particular alkoxysilane with fluorinated side chains (F‐silane) were deposited on Grade 420 stainless steel plates. Film amphiphobicity is characterized by measuring the water and oil contact angles of the coating. Film morphology is examined using atomic force microscopy. The deposited films free of F‐silane are thinner than 150 nm. The films become thick at high F‐silane volume percentage with the surface cavities, ridges, and granules being masked out. On the addition of F‐silane, the water contact angle of the deposited films increases up to 105° and then reaches a plateau of ～ 107° with increasing F‐silane. In contrast, the oil contact angle increases up to 60° at first and then slowly declines with the F‐silane concentration. The total drop of oil contact angle by ～ 20° was attributed to the masking out of surface features on film thickening. This indicates that the surface oleophobicity depends on surface structures. Therefore, improving surface amphiphobicity correlates with creating more refined multiscale surface structures during the industrial manufacturing process of steel plate, prior to surface modification by F‐silane. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 41003.     

Solution casting,characterization, and performance evaluation of perfluorosulfonic sodium type membranes for chlor‐alkali application

This investigation describes solution casting, characterization and performance evaluation of perfluorosulfonic sodium (PFSS) type membranes prepared by three different methods from Nafion solution and Nafion‐117 for Chlor‐Alkali (CA) application. A Chlor‐Alkali experimental set‐up was designed and constructed for performance evaluation of the recast membranes. The chemical structure of solution cast films was studied and confirmed by FTIR (Fourier Transform infrared spectroscopy) and ATR (Attenuated total reflection) techniques. The physical properties of solution cast films including mechanical strength, thermal behavior, water sorption, ion‐exchange capacity (IEC), morphology, and crystallinity were also evaluated. All the recast polymeric films behave like elastomers with low modulus but high elongation at break. Differential scanning calorimetric (DSC) thermograms of solution cast films showed two endothermic peaks at 180°C and 250°C attributed to matrix glass transition (T_gm) and ionic cluster glass transition (T_gc) of the Nafion polymer, respectively. The water uptake of polymeric films was reasonable in comparison with Nafion‐117. Solution casting has no significant effect on ion exchange capacity of the recast films. The scanning electron microscope (SEM) micrograph showed that the morphology of recast films is reasonably similar with Nafion‐117. However, the as‐cast films have some micro pores, which are produced during solution casting. The crystallinity of annealed film, because of the heat treatment was slightly high due to local ordering. According to the experimental results, which obtained from performance evaluation in CA cell, the properties of recycled films are similar to commercial membranes such as Nafion‐117 and can be used in CA process. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Self‐Expansion Behavior of Silk Fibroin Film

Summary: Silk fibroin cast film was prepared using a ternary solvent system of CaCl₂/CH₃CH₂OH/H₂O (1/2/8 in mole ratio). A drying temperature at casting influenced crystal structure of fibroin. When a drying temperature was set lower than 9 °C, the cast film became amorphous. When a drying temperature was set higher than 40 °C, a fibroin film of silk‐II structure was obtained. In order to produce a fibroin film of silk‐I structure, a preferable temperature range was from 20 to 26 °C. The crystal transformation from random coil structure into silk‐I could be made through exposure of an amorphous film to water vapor. As for the crystal transformation from silk‐I into silk‐II, the treatment with a glycerin solution was effective. In the course of the treatment a film showed self‐thinning and self‐expanding. The expansion ratio exceeded 40% at maximum. The film produced accompanying self‐expansion was ductile in nature.

The apparent self‐expansion percentage as a function of initial thickness of the film. The ductility of the film was classified into four stages from the observation of recovery behavior after folding: ?, very soft; ?, soft; ?, middle; ?, hard (see Figure 5 ).     

Annealing Effect on the Properties of Cu(In0.7Ga0.3)Se2 Thin Films Grown by Femtosecond Pulsed Laser Deposition

This work reports the crystallization, microstructure, and surface composition of CuIn_0.7Ga_0.3Se₂ (CIGS) thin films grown by femtosecond pulsed laser deposition at different annealing temperatures. The structural and optical properties of the CIGS films were characterized by X‐ray diffraction, Raman scattering, UV‐visible spectroscopy, and Hall effect measurement. The results indicate that binary crystals of CuSe initially formed on the as‐deposited film, but then completely turned into a quaternary chalcopyrite structure after annealing at 400°C. Phase transformation significantly affects the surface morphology, Hall properties, and band gap. Transmission electron microscopy further revealed that an interface between the Mo substrate and CIGS crystallites contains an amorphous layer even at the high temperature of 500°C. For the application of photovoltaic devices, we also report on the photoresponse of both as‐deposited and annealed films as demonstrated by preliminary tests.     

Studies on glass transition temperature of mono and bilayer protein films plasticized by glycerol and olive oil

Thermomechanical and thermal properties of whey protein, maize prolamin protein (zein), and the laminated whey protein–zein films were studied. The dynamic mechanical (thermal) analysis (DMTA) results showed that the single zein film had higher T_g than single whey protein and zein–whey laminated films. The shift in the T_g values of films from 31.2°C in whey protein film and 88.5°C in the zein film to 82.8°C in the laminated whey protein–zein films may be implied some interaction formation between the two polymers. The small tan δ peaks were observed at ?50°C in zein–glycerol films and at ?22.37°C in the whey protein films and can be related to β‐relaxation phenomena or presence of glycerol rich region in polymer matrix. Zein‐olive oil and zein–whey protein–olive oil films showed tan δ peaks corresponded the T_g values at 113.8, and 92.4°C, respectively. Thus, replacing of glycerol with olive oil in film composition increased T_g. A good correspondence was obtained when DSC results were compared with the tan δ peaks in DMTA measurements. DSC thermograms suggested that plasticizers and biopolymers remained a homogeneous material throughout the cooling and heating cycle. The results showed that T_g of zein–glycerol films predicted by Couchman and Karasz equation is very close to value obtained by DSC experiments. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Poly(L‐lactide). X. Enhanced surface hydrophilicity and chain‐scission mechanisms of poly(L‐lactide) film in enzymatic,alkaline, and phosphate‐buffered solutions

Attempts were carried out to enhance the surface hydrophilicity of poly(L ‐lactide), that is, poly(L ‐lactic acid) (PLLA) film, utilizing enzymatic, alkaline, and autocatalytic hydrolyses in a proteinase K/Tris–HCL buffered solution system (37°C), in a 0.01N NaOH solution (37°C), and in a phosphate‐buffered solution (100°C), respectively. Moreover, its chain‐scission mechanisms in these different media were studied. The advancing contact‐angle (θ_a) value of the amorphous‐made PLLA film decreased monotonically with the hydrolysis time from 100° to 75° and 80° without a significant molecular weight decrease, when enzymatic and alkaline hydrolyses were continued for 60 min and 8 h, respectively. In contrast, a negligible change in the θ_a value was observed for the PLLA films even after the autocatalytic hydrolysis was continured for 16 h, when their bulk M_n decreased from 1.2 × 10⁵ to 2.2 × 10⁴ g mol^?1 or the number of hydrophilic terminal groups per unit weight increased from 1.7 × 10^?5 to 9.1 × 10^?5 mol g^?1. These findings, together with the result of gravimetry, revealed that the enzymatic and alkaline hydrolyses are powerful enough to enhance the practical surface hydrophilicity of the PLLA films because of their surface‐erosion mechanisms and that its practical surface hydrophilicity is controllable by varying the hydrolysis time. Moreover, autocatalytic hydrolysis is inappropriate to enhance the surface hydrophilicity, because of its bulk‐erosion mechanism. Alkaline hydrolysis is the best to enhance the hydrophilicity of the PLLA films without hydrolysis of the film cores, while the enzymatic hydrolysis is appropriate and inappropriate to enhance the surface hydrophilicity of bulky and thin PLLA materials, respectively, because a significant weight loss occurs before saturation of θ_a value. The changes in the weight loss and θ_a values during hydrolysis showed that exo chain scission as well as endo chain scission occurs in the presence of proteinase K, while in the alkaline and phosphate‐buffered solutions, hydrolysis proceeds via endo chain scission. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 87: 1628–1633, 2003     

Degradation of red lead pigment in the oil painting during UV aging

The degradation product and mechanism of red lead pigment (Pb₃O₄, minium) in pure powder and in modeled oil painting are dynamically tracked during ultraviolet light aging by the change of color, crystal structure, chemical composition, and surface morphology. After UV aging, the color of pure minium pigment gradually darkens from bright orange‐red into black, but the color of model paint samples made by minium and tung oil binder changes into brownish and whitish color (ΔE^* = 56.60). After aging, the crystal structure of Pb₃O₄ powder is proved to transfer into plattnerite (β‐PbO₂) by X‐ray diffraction (XRD) pattern, but the degradation product of Pb₃O₄ in model paint samples is identified as 2PbCO₃·Pb(OH)₂ by the noticeable peaks at 24.8°, 27.4°, and 34.3° in XRD pattern, and two new Fourier transform infrared peaks at 1393 cm^?1 and 682 cm^?1 attributed to the presence of , and a new peak at 1051 cm^?1 in Raman spectroscopy. During UV aging, the model paint samples' surface is verified gradually from wrinkled surface into nanoscale sheet‐like structure and finally a regular hexagonal plate‐like crystal structure, showing hexagonal crystals of hydrocerussit 2PbCO₃·Pb(OH)₂. This reveals the interaction between organic tung oil binder and inorganic minium to accelerate the degradation of Pb₃O₄ pigment. Therefore, the degradation mechanism is deduced as that CO₂ and H⁺ formed by oxidizing ester/carboxyl groups in tung oil reacts with Pb²⁺ to yield the white product of 2PbCO₃·Pb(OH)₂. It is believed that this study will contribute much to the complete understanding of the degradation of minium pigment in oil paintings.     

Preparation and characterization of porous titanium dioxide sulfonated polystyrene composite microspheres with amphiphilicity

Porous particles with amphiphilicity were prepared by a nonpolymeric pore‐formation process with the sulfonation of polystyrene microspheres. Nano titanium dioxide (TiO₂) particles were then grafted onto the surface via a sol–gel method to finally form the composite particles. The effects of the mass ratio of ethanol (EtOH) to water, temperature, and solubility parameter on the pore‐formation process is discussed in detail. The morphology, porous structure, and wetting properties of the particles were studied by scanning electron microscopy, transmission electron microscopy, Fourier transform infrared (FTIR) spectroscopy, and contact angle measurement. The results show that porous sulfonated polystyrene (SP) microspheres could be fabricated at 60°C with a 1 : 1 mass ratio of EtOH–water and a solubility parameter of 29.69 MPa^1/2. The TiO₂ particles were determined to be grafted onto the SP microspheres by physical‐bond interaction on the basis of FTIR analysis. The contact angles for both water (aqueous‐phase) and various organic solvent (oil‐phase) droplets with different polarities on the surface of compressed tablets of TiO₂–SP powder were all lower than 30°; this indicated excellent amphiphilicity in the composite particles. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Working mechanism of poly(vinyl alcohol) cement fluid loss additive

The working mechanism of poly(vinyl alcohol) (PVA, M_w ～ 200,000 g mol^?1), a fluid loss control additive (FLA) applied in oil well cementing, was investigated. First, characteristic properties of PVA such as solubility and particle size in cold and hot water, minimum film forming temperature, adsorption on cement, viscosity of cement pore solution and static filtration properties of cement slurries treated with PVA were determined. It was found that the working mechanism of PVA relies on hydrated, but water‐insoluble PVA particles (d₅₀ ～ 2.4 μm). During cement slurry filtration, they coalesce into a polymer film. This film effectively plugs the pores of the cement filter cake. The sample studied here becomes water‐soluble at temperatures > 40°C (d₅₀ decreases to ～50 nm) and looses its effectiveness. Addition of highly anionic dispersants such as ß‐naphthalenesulfonate formaldehyde (BNS) or acetone formaldehyde sulfite (AFS) polycondensate extends the temperature range at which PVA works from 40°C to ～60°C. This effect is ascribed to lower solubility of PVA in the presence of these dispersants. The study reveals that decreased performance of PVA caused by higher temperatures is not the result of thermal degradation of the polymer, but is owed to its increasing water‐solubility. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Synthesis and characterization of a novel polyurethane curing agent modified by a diazafluorene derivative

In this study, we synthesized a novel polyurethane (PU) curing agent (CA) modified by the diazafluorene derivative, 9,9′‐di(4‐hydroxyphenyl)‐9‐1H‐4,5‐diazafluorene, at different hydroxyl ratios. The results of ¹H‐NMR and Fourier transform infrared spectroscopy proved the structure of the fluorine derivative and the modification of CAs. Differential scanning calorimetry and dynamic mechanical analysis showed that the glass‐transition temperature of the PU increased with the addition of the diazafluorene derivative, and the PU cured in the novel CA had more stable and better damping properties under moderate‐temperature conditions (30–80 °C) than the PU cured in the N75 CA. Tan δ was maintained in a relatively lower range shift in the moderate‐temperature range. The average adhesion values of the PU coating cured in the novel CA increased. The scanning electron microscopy morphologies of the PU film and the average adhesion of the coatings showed that the PU cured in the novel CA had good mechanical properties. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 46591.     

Hydrophobic and tribological behaviors of a poly(p‐phenylene benzobisoxazole) fabric composite reinforced with nano‐TiO2

1H,1H,2H,2H‐Perfluorooctyl trichlorosilane (PFTS) was used to modify TiO₂ nanoparticles, and hydrophobic PFTS–TiO₂ nanoparticles were obtained by an ultrasonic reaction method. The PFTS–TiO₂ surface morphological and hydrophobic properties were analyzed with scanning electron microscopy (SEM), Fourier transform infrared spectrometry, and contact angle (CA) testing. Then, the poly(p‐phenylene benzobisoxazole) fabric–phenolic composite filled with PFTS–TiO₂ as a lubricant additive was fabricated by a dip‐coating process. The tribological properties of the composite were investigated, and the wear surface morphology was observed by SEM. The experimental results show that the water CA of the composite filled with PFTS–TiO₂ was 158°, and the composite containing 4 wt % PFTS–TiO₂ exhibited excellent antifriction and abrasion resistance. The hydrophobic surface of the composite showed excellent durable performance with a static water CA of 126.7° after abrasion. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 45077.     

Conductive polypyrrole composite films prepared using wet cast technique with a pyrrole–cellulose acetate solution

Conductive polypyrrole‐cellulose acetate films were prepared from cellulose acetate (CA) solution of pyrrole (Py) using wet cast method. In the composite films, Py was used as a solvent for CA which was dissolved with different concentration. Then, to prepare PPy–CA composite film, the Py viscous solution of CA was cast on glass plate and immersed in FeCl₃ aqueous solution. When the CA film was formed in the aqueous solution, the polymerized PPy particles having about 1 μm diameter were formed in composite film. The resultant composite films were characterized, showing good film fabrication and electrical conductivity of around 6.9 × 10^?4 to 3.6 × 10¹ S/cm. POLYM. ENG. SCI., 54:78–84, 2014. © 2013 Society of Plastics Engineers