An acrylic resin emulsion containing a quaternary ammonium salt (hybrid q‐chitosan/acrylic resin emulsion) was prepared by emulsion polymerization using an acrylic monomer with and without DAAM. DAAM was used to incorporate a functional keto group into the acrylic resin emulsion. Furthermore, a hybrid chitosan/acrylic resin emulsion was prepared for comparison. The elution of q‐chitosan in water from the acrylic resin film with a keto group was less than that from the acrylic resin emulsion without a keto group. In addition, the mechanical properties of the hybrid q‐chitosan/acrylic resin film could be modified by q‐chitosan that was crosslinked between acrylic resin particles. Furthermore, hybrid q‐chitosan/acrylic resin films had adsorption ability for formaldehyde, and the antimicrobial properties of these films were superior to those of the hybrid chitosan/acrylic resin film.
Hybrid organic/inorganic acrylic nanostructured films were prepared by a UV/thermal dual‐curing process. The role of a fluorinated hydroxyl acrylate monomer (AF) as coupling agent was investigated. Increased Tg values and modulus of the dual‐cured films were achieved by increasing the TEOS inorganic precursor. The coupling agent deeply modified the surface properties of the cured films: the formation of hybrid films characterized by high hydrophobicity together with an increase on surface hardness was achieved. TEM analysis clearly evidenced the reducing of the nanosize dimensions of the inorganic silica domains by increasing the coupling agent content in the photocurable formulation.
Electrically conducting films containing AgNws, hydrophilic and hydrophobic resins were prepared. FT‐IR reveals that the interface between the AgNws and epoxy could be successfully modified by APTES. XPS shows that the AgNws were attracted by hydrogen bonds of ? NH2 and ? NH? groups after APTES modification. SEM analysis shows that the AgNws were well dispersed in the resin. The AgNws were also blended with hydrophilic and acrylic resins, and the resulting blends were compared with AgNws/epoxy blends. Results show that AgNw/PVA‐resin films possess the lowest surface electrical resistance. The AgNw/PVA‐resin and silane‐modified AgNw/epoxy resin conductive films possess a similar electrical percolation threshold.
In this study, novel protein/biodegradable polymer blend biomaterials‐gelatin/poly(ethylene oxide) blend films with compositional gradients were successfully fabricated by a dissolution/diffusion method. Two kinds of compositional gradient films, which were different in gradient structure, were prepared. The compositional gradient structure in the films was characterized by polarized optic microscopy, ATR‐FTIR, and trans‐FT‐IR mapping measurement. In addition, the mechanical properties of the gradient films were characterized with reference to their gradient structure. It is found that the compositional gradient films have better mechanical properties than the pure gelatin film. These protein/biodegradable polymer compositional gradient films have a potential for many biomedical applications.
Phenolic resin/clay composites were prepared by high‐shear mixing of clay suspended in CH3OH solutions of Novolac resin and curing agent. Pure clay Cloisite Na+ and pillared clays Cloisite 10A, 30B, and Na+Cloisite that was pillared by 3‐hexadecyl‐1‐methylimidazolium bromide were studied. After CH3OH evaporation, Novolac was cured at low temperatures. XRD showed that clay gallery d‐spacings decreased upon solvent evaporation and partial curing. Slight d‐spacing increases were sometimes observed from a partially cured stage to a further cured composite. Na+Cloisite gave the highest nanodispersion, Cloisites 10A and 30B the lowest. TGA revealed that Na+ clay or organoclay incorporation in partially cured and cured composites did not improve the thermal stability of Novolac.
Summary: Organic‐inorganic nanocomposite hybrid coatings were prepared through a dual‐cure process involving cationic photopolymerization of a hyperbranched epoxy functionalized resin and subsequent condensation of an alkoxysilane inorganic precursor. All the formulations investigated gave rise to photocured films characterized by high gel content values. An increase in glass transition temperature and an increase in storage modulus above Tg in the rubbery plateau is observed with increasing TEOS content in the photocurable formulation. The important role of GPTS on reducing the inorganic domain size and avoiding macroscopic phase separation was demonstrated by TEM analyses.
TEM obtained for one of the cured films in the presence of GPTS. 相似文献
Summary: In this study high‐refractive‐index polyimide/titania hybrid optical thin films were successfully prepared using a sol‐gel process combined with spin coating and multistep baking. The hybrid thin films were prepared from a soluble polyimide, a coupling agent, and a titania precursor. Transparent hybrid thin films can be obtained at TiO2 content as high as 40 wt.‐%. The FE‐SEM results suggest that the TiO2 particles in the hybrid thin films have diameters in the nanometer range. The thermal decomposition temperatures of the prepared hybrid materials are above those of the respective polyimide except for the highest TiO2 content hybrids. The refractive indices at 633 nm of the prepared hybrid thin films increase linearly from 1.66 to 1.82 with increasing TiO2 content. The excellent optical transparency, thermal stability, and tunable refractive index provide the potentials of the polyimide/titania hybrid thin films in optical applications.
Transparent light‐emitting hybrid materials are produced by UV curing of acrylic resins containing silica precursors and photoluminescent [Cu4I4L4] clusters. Acrylic double‐bond conversion is followed by means of FT‐IR spectroscopy, and optical measurements are performed on cured films showing a high transparency of the films up to a content of 30 wt% TEOS and a bright luminescence with a maximum of emission centered at 565 nm (yellow‐orange). This study shows the possibility to obtain new advanced materials in which functional properties such as photoluminescence and scratch resistance are successfully conjugated in a hybrid film that maintains high transparency.
This paper introduces an electroactive paper (EAPap) prepared with cellulose and chitosan films. The fabrication process, performance test, and the effect of acetic acid dosage of the EAPap were investigated. For the fabrication of cellulose EAPap, cellulose fibers were dissolved into a solution using N,N‐dimethylacetamide and lithium chloride. The solution was cast and immersed in water to form a cellulose film, followed by casting chitosan/acetic acid and glycerol aqueous solutions on the cellulose film. A bending EAPap actuator was made by depositing thin gold electrodes on both sides of the cellulose film. The bending displacement of the EAPap actuators was evaluated with respect to voltage, frequency, humidity, and acetic acid dosage. An optimum mole ratio of the acetic acid and chitosan structure unit was found. Also, the effects of chitosan and acetic acid on the actuation behavior of the cellulose‐chitosan laminated films were investigated.
Summary: In the present study (3‐methacryloxypropyl)trimethoxysilane (MPMS) containing acrylic resin/alumina hybrid materials with various alumina contents were prepared. The effects of ethylacetoacetate (EAA) content, catalyst type, and water content during sol–gel process for alumina sols on the microstructure and properties of the hybrid materials were investigated by SAXS, AFM, DSC, TGA, and nano‐indentation tester, respectively. It was found that the hybrid materials exhibited a homogeneity and the alumina phase of the hybrids had mass fractal dimension and open structure. The thermal and mechanical properties of the hybrid materials were obviously improved when alumina was incorporated. The EAA contents, catalyst type, and water content during sol–gel process for alumina sols had obvious effects on the microstructure and properties of the hybrid materials.
Typical load–displacement curves of the pure acrylic resin and hybrid materials with increasing alumina content. 相似文献
A fluorinated acrylic resin was synthesized for use as a co‐monomer with a commercially available epoxy resin for UV‐cured interpenetrating polymer network preparation. Hybrid IPN networks were achieved with morphology ranging from a co‐continuous IPN to complete phase separation simply by changing monomer ratios. Highly hydrophobic coatings with good adhesion properties on glass substrates were obtained.
The effects of the CTA concentration on polymerization kinetics, polymer microstructure, particle morphology, and adhesive performance of waterborne hybrid PSAs prepared by simultaneous free‐radical and addition miniemulsion polymerizations are studied. The development of the microstructure is shown to differ from waterborne acrylic PSAs obtained by free‐radical polymerization because of the contribution of the addition reaction, which in turn causes marked differences in the adhesive performance of the final films. A computer simulation is developed to obtain detailed information about the microstructure of PU/acrylic hybrids and to correlate the microstructure with the final adhesive properties.
Summary: In this work, epoxy resin/CaCO3 nanocomposites were prepared by in situ and inclusion polymerization. Nanoparticles with a size of 30–40 nm were dispersed efficiently in bisphenol‐A alkaline solution before polymerization and the dispersion could be kept in the resultant composite by a reaction that took place at the nanoparticle surface and among the nanoparticles when epichlorohydrin was added. Furthermore, the slightly conglomerated nanoparticles could even be separated by epoxy resin growing among them. This method showed a better dispersion of nanoparticles compared with solution‐blending as observed with TEM. Owing to better combination of epoxy resin and nanoparticles, the resultant nanocomposite showed a 12 °C increase in Tg compared to the nanocomposite prepared by solution‐blending. Tensile test revealed that the tensile strain of nanocomposites rises as the nano‐CaCO3 content increases.
The dispersion mechanism of nanoparticles through in situ and inclusion polymerization. 相似文献
Surface properties of epoxy coatings are modified by PDMS additives in cationic UV curing of a cycloaliphatic epoxy resin. The cured films show a very high hydrophobicity that does not depend on PDMS concentration, indicating that a threshold is reached even at 0.3 wt% additive. A slight increase of the water contact angle as a function of PDMS molecular weight is observed. The additive selectively modified the air‐side of the film, while the glass‐side retains the surface properties of the pure resin. This segregation phenomenon permits to obtain highly hydrophobic films with still good adhesion properties on polar substrates, which is an important advantage over common surface‐modified resins.
A dual‐cure latex is prepared by mixing an amide‐functionalized latex with a latex that has both acetoacetoxy and unsaturated acrylic functionalities. The amide‐functionalized latex provides a thermal cure with the acetoacetoxy groups of the other latex via Michael addition. The partially polymerized triacrylates in the acrylate‐functionalized latex provide active sites for photocuring. Thermoset latex films are prepared by blending amide‐ and acrylate‐functionalized latexes in varying amounts. The effect of the photosensitizer (camphorquinone) concentration on thermal and mechanical properties is studied. The highest tensile modulus and elongation is observed in a 50:50 wt% amide/acrylate‐functionalized latex blend.
Acrylic‐epoxy interpenetrating polymer networks were prepared by means of UV curing. The photopolymerization process was investigated via real‐time FTIR spectroscopy. The hybrid, cured films showed a broad tan δ peak in DMTA demonstrating the high damping properties of the hybrid, cured formulations. A decrease on shrinkage was achieved by increasing the epoxy‐resin content in the photocurable formulation, with a consequent increase in adhesion properties.
Cardanol, a well known natural resource, was used to produce a polymer resin in the presence of formaldehyde, catalyzed by H2SO4. Before reticulation, PAni · H2SO4 was blended with the resin. The blended material was cast into poly(propylene) cups and kept inside a desiccator under vacuum until complete water evaporation. The final in situ polymer blend was solid and could not be dissolved in ordinary solvents, indicating that a reticulated material had been obtained. Samples prepared similarly were then characterized, showing that the produced blends can be used as pressure sensing materials.
Summary: Contact‐mode AFM adhesion strength measurements were employed in order to investigate the capability of PBBMA FR as an adhesion promoter in PP composites. The reactive FR exhibited superior coupling properties in comparison to conventional coupling agents such as PP‐g‐ma introduced in reinforced PP composites.
AFM image showing the recess carved out by the AFM tip in a PBBMA layer deposited on glass treated with APS. 相似文献
Summary: An alkyl‐functionalized hyperbranched polymer, HBP(OH)–C16, was synthesized by partial modification with fatty acid of an aromatic‐aliphatic OH‐terminated hyperbranched polyester HBP? OH. This product was used as additive in the cationic photopolymerization of an epoxy resin. The alkyl‐modified polyester takes part in the photopolymerization process thanks to the residual OH groups by means of chain‐transfer reactions. An increase of the epoxy conversion is observed by increasing the amount of the HBP additive in the photocurable resin with a modification of the bulk properties of the final ultraviolet‐cured films. The presence of HBP(OH)–C16 induces an increase in glass transition temperature, thermal stability, and solvent resistance. Moreover the surface properties of the films are modified achieving highly hydrophobic surfaces in the presence of even very low amounts of HBP(OH)–C16.
Summary: Films of poly(L ‐lactic acid) (PLLA) and copolymers of L ‐lactide (LLA) with either glycolide [P(LLA‐GA)](81/19) or D ‐lactide [P(LLA‐DLA)](77/23) were prepared and an effect of comonomer type on the hydrolytic degradation of the films was studied in phosphate‐buffered solutions at 37 °C. The degraded films were investigated using gravimetry (weight loss and water absorption), gel permeation chromatography, DSC, X‐ray diffractometry, tensile testing and polarization optical microscopy. To exclude the effects of molecular weight and crystallinity on hydrolytic degradation, the films were prepared from polymers with similar molecular weights and were made amorphous by melt quenching. It was found that the hydrolytic degradation rate decreased in the order P(LLA‐GA) > P(LLA‐DLA) > PLLA. The hydrolytic degradation rate constant of PLLA and LLA copolymer films increased with increasing the water absorption (hydrophilicity), or with decreasing the initial glass transition temperature or the L ‐lactyl unit sequence length, indicating that the hydrolytic degradation rate of the copolymers was closely related to these three parameters. The crystallization of P(LLA‐GA) film occurred within hydrolytic degradation for 20 weeks.
Mn of PLLA and LLA copolymer films as a function of hydrolytic degradation time. 相似文献
