Synthesis of UV crosslinkable waterborne siloxane–polyurethane dispersion PDMS-PEDA-PU and the properties of the films

A UV crosslinkable waterborne siloxane–polyurethane dispersion, PDMS-PEDA-PU, was synthesized by incorporating acrylate groups into the side chain of the polyurethane using pentaerythritol diacrylate (PEDA). Polysiloxane groups were introduced into the soft segment of the polyurethane using polydimethylsiloxane (PDMS). They formed a crosslinking structure after UV radiation. The structure of PDMS-PEDA-PU was confirmed by the use of Fourier transform infrared spectroscopy (FTIR). X-ray diffraction (XRD) analysis indicated that the formed PDMS-PEDA-PU was amorphous. The curing rule of PDMS-PEDA-PU was investigated on the basis of the change in C=C conversion during the UV curing process. The influence of the PDMS/PEDA ratio was studied with respect to the water resistance, the thermal property, and the mechanical property of the films.     

Poly dimethylsiloxane/carbon nanofiber nanocomposites: fabrication and characterization of electrical and thermal properties

This article presents the fabrication and characterization of poly dimethylsiloxane/carbon nanofiber (CNF)-based nanocomposites. Although silica and carbon nanoparticles have been traditionally used to reinforce mechanical properties in PDMS matrix nanocomposites, this article focuses on understanding their impacts on electrical and thermal properties. By adjusting both the silica and CNF concentrations, 12 different nanocomposite formulations were studied, and the thermal and electrical properties of these materials were experimentally characterized. The developed nanocomposites were prepared using a solvent-assisted method providing uniform dispersion of the CNFs in the polymer matrix. Scanning electron microscopy was employed to determine the dispersion of the CNFs at different length scales. The thermal properties, such as thermal stability and thermal diffusivity, of the developed nanocomposites were studied using thermogravimetirc and laser flash techniques. Furthermore, the electrical volume conductivity of each type of nanocomposite was tested using the four-probe method to eliminate the effects of contact electrical resistance during measurement. Experimental results showed that both CNFs and silica were able to impact on the overall properties of the synthesized PDMS/CNF nanocomposites. The developed nanocomposites have the potential to be applied to the development of new load sensors in the future.     

Preparation and coating properties of an acrylic melamine resin containing silicone segments

The aim of this study was the preparation of novel water repellent UV curable materials using acrylic modified melamine (AM) and poly-dimethylsiloxane (PDMS). UV curable acrylic melamines containing silicone segments (SiAMs) were synthesized by condensation of methylolmelamine, 2-hydroxyethyl acrylate, and carbinol-modified PDMS. The SiAM films with a 0.3 wt% PDMS segment that were cured by UV irradiation had higher transparency than that of a blended sample. Examination with a scanning electron microscope revealed that the blend sample has cohesion of the silicone segments, while such a phenomenon was not observed in the composite samples (SiAMs). From these results, it was confirmed that aggregation of the silicone segments was prevented by introducing the silicone segments into the acrylic melamine. By introducing 0.3 wt% of PDMS segments into AM, good water-shedding properties were confirmed, while several of the most attractive features of AM, such as hardness, adhesion, and refractive index, were maintained.     

Post Curing as an Effective Means of Ensuring the Long-term Reliability of PDMS Thin Films for Dielectric Elastomer Applications

Post curing can be used to facilitate volatile removal and thus produce polydimethylsiloxane (PDMS) films with stable elastic and electrical properties over time. In this study, the effect of post curing was investigated for commercial silicone elastomer thin films as a means of improving long-term elastomer film reliability. The Young’s moduli and electrical breakdown strengths of commercial (silica-reinforced) PDMS elastomer films, with and without additional 35 parts per hundred rubber titanium dioxide (TiO₂), were investigated after high-temperature (200°C) post curing for various time spans. The elastomers were found to contain less than 2% of volatiles (significantly higher for TiO₂-filled samples), but nevertheless a strong effect from post curing was observed. The young’s moduli as well as the strain-dependent behavior were found to change significantly upon post curing treatment, where Young’s moduli at 5% strain increase with post curing. Furthermore, the determined dielectric breakdown parameters from Weibull analyses showed that greater electrical stability and reliability could be achieved by post curing the PDMS films before usage, and this method therefore paves a way toward more reliable dielectric elastomers.     

UV‐curing and mechanical properties of polyester–acrylate nanocomposites films with silane‐modified antimony doped tin oxide nanoparticles

Antimony doped tin oxide (ATO) nanoparticles were used as nanofillers to improve mechanical properties of UV‐cured polyester–acrylate films. To improve the dispersion of ATO nanoparticles in the polyester–acrylate resin matrix and to strengthen interfacial interactions between ATO nanoparticles and the resin matrix ATO nanoparticles were first organically modified with 3‐methacryloxypropyltrimethoxysilane (MPS). The modification of ATO nanoparticles with MPS was confirmed by FTIR spectroscopy and thermogravimetric analysis (TGA). UV‐curing behaviors of the nanocomposites films were investigated by FTIR spectroscopy. Compared with the film with neat ATO nanoparticles, the film with the same amount of MPS‐modified ATO nanoparticles showed slightly higher UV‐curing rate and final conversion. The mechanical properties of the nanocomposites films were measured by universal testing machine. The MPS‐modified ATO nanoparticles could improve considerably the mechanical properties of the UV‐cured polyester–acrylate nanocomposites films. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Physical properties of Al-doped ZnO films deposited on nonwoven substrates by radio frequence magnetron sputtering

In this study, the polyethylene terephthalate (PET) spunbonded nonwoven materials were used as substrates for creating electro-optical functional nanostructures on the fiber surfaces. A magnetron sputter coating was used to deposit Al-doped ZnO (AZO) films onto the nonwovens. The influences of the deposition time on the structural, optical, and electrical properties of AZO films were investigated. Atomic force microscopy (AFM) was employed to examine the topography of the fibers. The AFM observation revealed a significant difference in the morphology of the fibers before and after the AZO sputter coating. The examination by UV–visible spectrophotometer analysis showed that the nonwovens deposited with transparent nanostructure AZO films had better UV absorption, and an average transmittance was approximately 50% in the visible light wavelength region. The surface conductivity of the materials was analyzed using a four-probe meter, and it was found that electrical resistance was significantly decreased as the sputtering time increased.     

Effect of surface modification of titanium dioxide on the UV-C aging behavior of silicone rubber

Surface modification of titanium dioxide (TiO₂) nanoparticles (NPs) by silane coupling agents and the ultraviolet-C (UV-C) aging behavior of silicone rubber (SiR) incorporated with the modified TiO₂ NPs were investigated in this work. The SiR samples incorporated with TiO₂ NPs displayed excellent stability against the UV-C radiation. In order to improve the dispersion of TiO₂ NPs in the SiR matrix, the surface of TiO₂ NPs was modified with 3-aminopropyl triethoxysilane and 3-trimethoxysilyl propyl methacrylate, respectively. The surface modification of TiO₂ NPs was characterized by thermal gravimetric analysis and Fourier transform infrared spectroscopy. The dispersion stability of the pristine TiO₂ NPs and surface silane-modified TiO₂ NPs was evaluated in an organic solvent (toluene). Effect of surface modified TiO₂ NPs on the UV-C aging behavior of SiR was evaluated in terms of the change of surface morphology, tensile properties, hardness, crosslinking density, and surface microstructure before and after the UV-C aging. The results showed that surface modification of TiO₂ NPs with silane coupling agents could improve the dispersion of TiO₂ NPs in the SiR matrix. Moreover, the SiR with modified TiO₂ NPs showed an improved aging resistance to the UV-C radiation, compared with the samples with pristine TiO₂ NPs. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47170.     

Preparation and properties of poly(urethane acrylate) (PUA) and tetrapod ZnO whisker (TZnO‐W) composite films

Tetrapod zinc oxide whiskers (TZnO‐Ws) were successfully synthesized via a thermal oxidation method and confirmed using Fourier transform infrared spectroscopy, X‐ray diffraction and scanning electron microscopy. A series of poly(urethane acrylate) (PUA)/TZnO‐W composite films with various TZnO‐W contents were prepared via a UV curing method and their physical properties were investigated to understand their possible use as packaging materials. The morphological, thermal, mechanical, antibacterial and barrier properties of the PUA/TZnO‐W composite films were interpreted as a function of TZnO‐W content. The thermal stability, barrier properties and antibacterial properties of the composite films, which were strongly dependent upon their chemical and morphological structure, were enhanced as the TZnO‐W content increased. The oxygen transmission rate and water vapor transmission rate decreased from 614 to 161 cm³ m^?2 per day and 28.70 to 28.16 g m^?2 per day, respectively. However, the mechanical strength of the films decreased due to the low interfacial interaction and poor dispersion with high TZnO‐W loading. The enhanced barrier properties and good antibacterial properties of the PUA/TZnO‐W composite films indicate that these materials are potentially suitable for many packaging applications. However, further studies are needed to increase the compatibility of polymer matrix and filler. © 2012 Society of Chemical Industry     

Simultaneous Laser‐Induced Reduction and Nitrogen Doping of Graphene Oxide in Titanium Oxide/Graphene Oxide Composites

Titanium oxide/graphene oxide nanocomposite thin films were grown by ultraviolet (UV) matrix‐assisted pulsed laser evaporation (MAPLE) technique in controlled oxygen or nitrogen atmospheres. The effect of graphene oxide addition and laser‐induced reduction as well as nitrogen doping on the wetting behavior and photoactive properties of titanium oxide thin films was investigated. Hydrophobic to hydrophilic conversion of titanium oxide films takes place progressively as the relative amount of graphene oxide in the MAPLE composite target increases. Nitrogen doping leads to further decrease of the static contact angle of the composite films. The photoactive properties of the synthesized materials were investigated through the evolution of contact angle under UV light irradiation. Wetting properties of both TiO₂ and TiO₂/GO nanocomposite thin films improved upon exposure to UV light.     

Mechanical,surface, and thermal properties of polyamideimide–polydimethylsiloxane nanocomposites fabricated by sol–gel process

Polyamideimide (PAI)–epoxysilane (coupling agent) composites were reacted with oligomeric polydimethylsiloxane (PDMS), a condensation product of difunctional silane, by using the sol–gel process, and were then dried into films. After this procedure, the surface, mechanical, and thermal properties were measured. The study showed that PDMS existed in the PAI matrix by the use of FTIR. With respect to mechanical properties, the maximum elongation and toughness were increased in the PAI with silane groups, although the maximum tensile strength was slightly decreased. In this experiment, PAI–30 wt % epoxysilane composite had the best mechanical properties. The intensive dispersion of the silane groups on the surface of PAI was confirmed through XPS measurement. As a function of the siloxane contents, the TGA curve shows less thermal stability in terms of their initial weight loss. However, in an oxygen atmosphere at about 700°C, the series of PAI–siloxane composites indicated a significant increase in char concentration. In the end, PAI with a relevant amount of silane groups was improved in both toughness and surface properties. This experiment showed that PDMS added to PAI had better properties than those of classical materials. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 91: 1774–1783, 2004     

Structural,thermal, micromechanical and electrical study of polyimide composite thin films incorporating indium tin oxide

Studies of composite films incorporating inorganic materials are of immense importance for current technological applications. Polyimide (PI) composite thin films incorporating indium tin oxide (ITO) at various weight ratios were processed using an in situ generation approach. The resultant product was imidized up to 350 °C to test the ability of the material to endure high temperatures without affecting the host matrix. The morphological behaviour of the PI/ITO composite films was investigated using Fourier transform infrared, scanning electron microscopy and atomic force microscopy characterization techniques. The degrees of crystallinity and ITO particle size within the PI matrix were studied using X‐ray diffraction. The thermal, structural and electrical properties were analysed using thermogravimetric analysis, differential scanning calorimetry, UV‐visible spectroscopy and the four‐probe technique. The micromechanical properties of the composites were evaluated in terms of tensile strength, tensile modulus and elongation. An overall improvement in the properties of the composite films was observed in comparison to those of pure PI. The synergistic improvement in the composite films is associated with the interaction mechanism between ITO and PI, where ITO becomes dispersed and interacts within the PI matrix. This leads to a decrease in available free‐space volume and increases the surface enrichment providing reinforcement to the matrix. Copyright © 2010 Society of Chemical Industry     

Preparation and properties of poly(propylene carbonate) and nanosized ZnO composite films for packaging applications

A series of polypropylene carbonate (PPC)/ZnO nanocomposite films with different ZnO contents were prepared via a solution blending method. The morphological structures, thermal properties, oxygen permeability, water sorption, and antibacterial properties of the films were investigated as a function of ZnO concentration. While all of the composite films with less than 5 wt % ZnO exhibited good dispersion of ZnO in the PPC matrix, FTIR and SEM results revealed that solution blending did not lead to a strong interaction between PPC and unmodified ZnO. As such, poor dispersion was induced in the composite films with a high ZnO content. By incorporating inorganic ZnO filler nanoparticles, the diffusion coefficient, water uptake in equilibrium, and oxygen permeability decreased as the content of ZnO increased. The PPC/ZnO nanocomposite films also displayed a good inhibitory effect on the growth of bacteria in the antimicrobial analysis. The enhancement in the physical properties achieved by incorporating ZnO is advantageous in packaging applications, where antimicrobial and environmental‐friendly properties, as well as good water and oxygen barrier characteristics are required. Furthermore, UV light below ～ 350 nm can be efficiently absorbed by incorporating ZnO nanoparticles into a PPC matrix. ZnO nanoparticles can also improve the weatherability of a PPC film. In future research, the compatibility and dispersion of the PPC matrix polymer and the inorganic ZnO filler nanoparticles should be increased. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011.     

Epoxy composites with carbon nanotubes and graphene nanoplatelets – Dispersion and synergy effects

Carbon nanotubes (CNTs) and graphene nanoplatelets (GNPs) at different mix ratios were dispersed by ultrasonication into an epoxy matrix and the effects of CNT:GNP ratios on the mechanical and electrical properties of the hybrid composites were investigated. The combination of CNT and GNP in a ratio 8:2 was observed to synergistically increase flexural properties and to reduce the electrical percolation threshold for the epoxy composites, indicating easier formation of a conductive network due to the improved state of CNT dispersion in the presence of GNPs. The state of dispersion was evaluated at different length scales by using optical microscopy, UV–Vis spectroscopy, rheological measurements, scanning electron microscopy, transmission electron microscopy and sedimentation tests. The Fourier transform infrared spectra for CNT and GNP indicate that the GNPs contain oxygen moieties responsible for better interactions with the epoxy matrix.     

Cu and Ag Nanoparticles Films Deposited on Glass Substrate Using Cold Cathode Ion Source

Structural, electrical and optical properties of Cu and Ag nanoparticles thin films deposited on glass substrates prepared by sputtering were investigated. Cold cathode ion source used for sputtered of copper and silver targets to deposit nanoparticles thin films on glass substrate using argon gas. X-ray diffraction was used to study the structure and the grain size of thin film which reveals that average grain size is in nano region. Copper nanoparticles was in rang 14 nm and silver nanoparticles size was 20 nm in first peak using Scherrer’s method. The electrical resistivities of copper and silver thin films were also investigated. The thin film resistance Rs of Cu and Ag equals 1.33 and 6.35 Ω respectively. I-V characteristics of thin films were recorded at room temperature and are found to be linear. Optical properties of the synthesized materials are studied by UV–Vis in the wavelength range 200–800 nm. The calculated band gap for the Cu thin film on glass are estimated to be E_gCu = 2.18 eV.     

Large strain and toughness enhancement of poly(dimethyl siloxane) composite films filled with electrospun polyacrylonitrile-graft-poly(dimethyl siloxane) fibres and multi-walled carbon nanotubes

Unfilled cross-linked poly(dimethyl siloxane) (PDMS) is a weak material and is generally filled with high levels of particulate fillers such as silica, calcium carbonate and carbon black to improve its mechanical properties. The use of fibrous fillers such as electrospun nanofibres and multi-walled carbon nanotubes as fillers for PDMS has not been widely studied. In this study anew copolymer, polyacrylonitrile-graft-poly(dimethyl siloxane) (PAN-g-PDMS), is used as fibrous filler for PDMS. The graft copolymer is electrospun to produce the fibre filler material. It is shown how the PDMS content of the graft copolymer provides increased compatibility with silicone matrices and excellent dispersion of the fibre fillers throughout a silicone matrix. It is also shown that it is possible to include multi-walled carbon nanotubes in the electrospun fibres which are subsequently dispersed in the PDMS matrix. Fibre mats were used in the non-woven and the aligned forms. The differently prepared fibre composites have significantly different mechanical properties. Conventional composites using fibrous fillers usually show increased strength and stiffness but usually with a resultant loss of strain. In the case of the composites produced in this study there is a dramatic improvement in the extensibility of the non-woven PAN-g-PDMS fibre mat filled silicone films of up to 470%.     

Evaluation of cross‐linking after accelerated photo‐ageing of silicone rubber

Silicone formulations based on polydimethylsiloxane (PDMS) were investigated by using a number of analytical techniques. Horizontal attenuated total reflectance Fourier‐transform infrared (HATR‐FTIR) spectroscopy studies have confirmed the stability of these materials towards photo‐oxidation. No significant oxygenated products were detected after 5000 h of accelerated photo‐ageing. However, by using thermoporosimetry, hardness measurements and densitometry, an important vulnerability of these formulations towards the cross‐linking reactions provoked by UV visible radiation was identified. Thermoporosimetry, using the solid‐solid cyclohexane transition as a textural probe, was also used to visualize the profile of cross‐linking inside the materials by calculation of the mesh size distribution in successive slices of 40 µm in thickness. Copyright © 2003 Society of Chemical Industry     

Radiation resistant metal decorated MWCNTs/PMMA nanocomposite films with enhanced thermomechanical properties

UV/O₃ radiation and chemical resistant nanocomposite films of functionalized/metal decorated multiwall carbon nanotubes (MWCNTs) with polymethylmethacrylate (PMMA) are synthesized. Silver nanoparticles are decorated on the surface of UV/O₃ functionalized MWCNTs by both reduction and in situ growth from AgNO₃ aqueous solution. Microscopic studies reflect the better dispersion of UV/O₃ functionalized/silver decorated MWCNTs in polymer matrix contributing in enhancement of thermal stability, thermomechanical strength, glass transition temperatures, and thermal conductivity of nanocomposites even at 0.25 wt% MWCNTs additions. The thermal stability of nanocomposite film (0.25 wt% loading), prepared by using a surfactant (Sodium dodecyl sulfate) is increased to about 27°C while the thermomechanical properties are raised up to 76% at 100°C. Thermal and thermomechanical behavior of pre‐ and post‐UV/O₃ irradiated nanocomposite films are compared with neat polymer. The results reveal that UV/O₃ functionalized MWCNTs can effectively disperse the radiation and have a dramatic reinforcement effect on the nature of the degradation of PMMA matrix. POLYM. COMPOS., 36:969–978, 2014. © 2014 Society of Plastics Engineers     

Poly(3-hexylthiophene) wrapped carbon nanotube/poly(dimethylsiloxane) composites for use in finger-sensing piezoresistive pressure sensors

We fabricated a piezoresistive composite using multi-walled carbon nanotubes (MWCNTs) as a conductive filler and polydimethylsiloxane (PDMS) as a polymer matrix, which operated in the extremely small pressure range required for finger-sensing. To achieve a homogeneous dispersion of MWCNTs in PDMS, the MWCNTs were modified by a polymer wrapping method using poly(3-hexylthiophene) (P3HT). The percolation threshold of the composites was significantly lowered by the presence of P3HT. The electrical conductivity and piezoresistive sensitivity of the composite were found to strongly depend on the P3HT concentration. The well-dispersed P3HT-MWCNT/PDMS composite showed good piezoresistive characteristics in the 0–0.12 MPa pressure range.     

Investigating the effect of silver nanorods embedded in polydimethylsiloxane matrix using nanoindentation and its use for flexible electronics

The stretchable electrodes with excellent flexibility, electrical conductivity, and mechanical durability are the most fundamental components in the emerging and exciting field of flexible electronics. This article proposes a method for fabrication of such a stretchable electrode by embedding silver nanorods (AgNRs) into a polydimethylsiloxane (PDMS) matrix that is grown by a unique glancing angle deposition technique. The surface, mechanical, and electrical properties of PDMS are significantly changed after embedding the AgNRs in it. The results show that surface roughness and polarity increase after AgNRs are embedded in the PDMS matrix. Elastic modulus (E) and hardness (H) decrease with an increase in the indentation load as a result of the indentation depth effect. Due to strong interfacial adhesion of AgNRs embedded in the PDMS matrix, the E and H of nanocomposite are increased by 167.6 and 93.3% compared with PDMS film, respectively. Furthermore, the AgNRs-PDMS film has an electrical resistivity value in the order of 10⁻⁷ Ωm. It remains conductive during various mechanical strains such as bending, twisting, and stretching, which is demonstrated using a light-emitting diode circuit. Simultaneously, the antimicrobial activity of silver could make it a promising candidate for wearable electronics.