In situ Measurement of the Adhesion Strength and Effective Elastic Stiffness of Single Soft Micropillar

We report the deformation behavior and mechanical properties of a polymeric micropillar, which measures approximately 10 μm by 30 μm in size by measuring the loading/unloading response using an in situ force measurement system. When the single poly(dimethylsiloxane) (PDMS) micropillar was subjected to compression, we observed a periodic wrinkle and global (Euler) buckling at the sidewall. During unloading, we found the pull-off force (adhesion force) to increase for higher values of preloading and also for lower loading/unloading rates. From the slope of the load–displacement curves measured in situ, we calculated the effective elastic stiffness of the PDMS micropillar to be about 2.03 MPa. In addition to the current work, we report that this method can be used more broadly for in situ measurement of the intrinsic mechanical and adhesion properties of polymers and other relatively soft materials.     

Synthesis of a Series of PEG-Based ABA Triblock Copolymers and Their Influence on Rheology of Cement Slurries

A series of water-soluble ABA triblock copolymers consisting of a polyethylene glycol central block joined to two blocks of six different homopolymers have been synthesized via simple solvent-free and ecofriendly routes and characterized by FTIR and ¹HNMR spectroscopy. Dispersing and slump-retaining abilities of the copolymers in cement slurries were evaluated by mini-slump spread method. Rheological measurements of samples with the best performance were carried out using a rate-controlled coaxial cylinder viscometer. The test results indicate that the dispersing power of the copolymers in cement pastes is strongly affected by the structure and degree of polymerization of the monomers.     

Thin-film nanofiltration membrane with monomers of 1,2,4,5-benzene tetracarbonyl chloride and ethylene diamine on electrospun support: preparation,morphology and chlorine resistance properties

Polymer Bulletin - Novel polyimide nanofiltration membranes were prepared by interfacial polymerization using 1,2,4,5-benzene tetracarbonyl chloride (BTC) and trimesoyl chloride solution in...     

Synthesis of biocompatible and degradable microspheres based on 2‐hydroxyethyl methacrylate via microfluidic method

Monodisperse poly(2‐hydroxyethyl methacrylate), p‐HEMA, microspheres in size ranging from 16 to 340 (μm) were synthesized by in situ emulsion photopolymerization of HEMA monomer with polyethylene glycol diacrylate (p‐EGDA) by means of a three‐dimensional microfluidic flow‐focusing device. An aqueous solution of HEMA, p‐EGDA as chain extender and UV‐photoinitiator serving as dispersed phase formed microdroplets in a continuous oil phase mainly consisting of n‐heptane. A downward coaxial orifices design in the device led to confinement of the reaction admixtures thread to central axis of the microchannels. This design strategy could solve the wetting problem of dispersed phase with the microchannels leading to a successful production of monodisperse microspheres with size variation of less than 4%. The effects of concentration of p‐EGDA, surfactant, and flow rate ratios on microsphere size were examined. It was observed that increasing the concentration of p‐EGDA slightly increases the size whereas increasing the flow rate ratios of continuous to dispersed phase effectively decreases the size of microspheres. The rapid continuous synthesis of p‐HEMA based microspheres via the microfluidic route with reliable control over size, size distribution, and composition opens new doors for mass production of biocompatible and degradable polymeric microspheres for enormous biotechnological applications. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40925.     

Influence of Ni/Co binders and Mo2C on the microstructure evolution and mechanical properties of (Ti0.93W0.07)C–based cermets

In this research, solid–solution powder of (Ti_0.93W_0.07)C was synthesized by high–energy ball mill method followed by carbothermal reduction process. Subsequently, the acquired powder was blended with Ni/Co and Mo₂C secondary carbide, and sintered under the optimized temperature (1510?°C) for 1?h to produce the modulated cermets. A typical core–rim structure formation with solid–solution phases was confirmed by backscattered electrons studies using a Field Emission electron scanning microscope. The hardness of the synthesized cermets was enhanced by increasing the specific amount of Mo₂C. The acquired results demonstrate that the binder type has a prominent influence on the microstructure and hardness of the prepared cermets. The hardness of (Ti_0.93W_0.07)C–xMo₂C–Ni cermet increased ~ 9%, when nickel was partially substituted by cobalt.     

Nanomechanical and tribological behavior of hydroxyapatite reinforced ultrahigh molecular weight polyethylene nanocomposites for biomedical applications

A hydroxyapatite (HA) particulate reinforced ultrahigh molecular weight polyethylene (UHMWPE) nanocomposite is fabricated by internal mixer at 180°C and using of paraffin oil as a processing aid to overcome the high viscosity of melted UHMWPE. The reinforcing effects of nano‐HA are investigated on nanomechanical properties of HA/UHMWPE nanocomposites by nanoindentation and nanoscratching methods. Results show that the nanocomposite with 50 wt % nano‐HA exhibits a Young's modulus and hardness of 362.5% and 200% higher, and a friction coefficient of 38.86% lower than that of pure UHMWPE, respectively. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42052.     

Electropolymerization and characterization of polyaniline, poly(2-anilinoethanol) and poly(aniline-co-2-anilinoethanol)

Applications of conducting polymers to biosensors have recently aroused much interest. This is because these molecular electronic materials offer control of different parameters such as polymer layer thickness, electrical properties and bio-reagent loading, diversity, ease of fabrication and potentially low cost, etc. Polyaniline, poly(2-anilinoethanol) and poly(aniline-co-2-anilinoethanol) preparations are performed with electrochemical (CV) method at room temperature, in a standard three-electrode cell. Homopolymer and the copolymers of aniline and 2-anilinoethanol films were deposited from 1?M acidic aqueous media containing 0.2?M aniline, 2-anilinoethanol by voltammetric sweep between ?0.1 and 1 V Ag/AgCl, at 20?mV/s^?1. The sweep was stopped after 30 cycles at ?0.1?V Ag/AgCl and the working electrode was covered by homopolymer and copolymer of aniline and 2-anilinoethanol. Characterizations of the products were carried out by cyclic voltammograms, UV?Cvisible, differential scanning calorimetry (DSC), Fourier transform infrared spectroscopy (FTIR) and electrochemical impedance (EIS) was employed to examine the water absorption of the synthesized polymers to be used in biosensor application. Electrochemical properties of polyaniline, poly(2-anilinoethanol) and poly(aniline-co-2-anilinoethanol) were studied and it is shown that with increased (2-anilinoethanol) content in the copolymer, its electroactivity, conductivity and resistance are reduced, though the processability and adhesion properties improve. The hydrophilicity of polymer film obtained has increased with increasing (2-anilinoethanol) content which leads to salt moving to the surface of steel.     

Properties of PET/clay nanocomposite films

Polyethylene terephthalate (PET) nanocomposite films were prepared by cast extrusion followed by uniaxial stretching, using chill rolls. Transmission electron microscopy (TEM) and wide angle X‐ray diffraction (WAXD) showed that the clay layers were aligned in the machine direction (MD) in the PET/clay nanocomposite (PCN) films. Differential scanning calorimetry (DSC) showed that PCN films have higher crystallinity than the neat PET films, possibly due to the nucleating role of the silicate layers. The PCN films became hazier as the clay content increased, but the film transparency remained in the acceptable range. Oxygen permeability of the PCN films decreased by 23% compared to the neat PET film. This is comparable with predictions of models proposed in the literature. Silicate incorporation brought about 20% increase in the tensile modulus, while the puncture and tear propagation resistance were reduced, due to brittleness of the PCN films. The measured modulus (1.7 GPa) was somewhat smaller than the values predicted using the Pseudoinclusion model (2.1 GPa). POLYM. ENG. SCI., 2012. © 2011 Society of Plastics Engineers     

Controlled release of prednisolone acetate from molecularly imprinted hydrogel contact lenses

The aim of this work was to study the influence of methacrylic acid (MAA) as a comonomer and the application of a molecular imprinting technique on the loading and release properties of weakly crosslinked 2‐hydroxyethyl methacrylate (HEMA) hydrogels, with a view toward their use as reloadable soft contact lenses for the administration of prednisolone acetate (PA). The hydrogels were prepared with HEMA (95.90–98.30 mol %) as a backbone monomer, ethylene glycol dimethacrylate (140 mM) as a crosslinker, and MAA (0, 50, 100, or 200 mM) as a functional monomer. Different PA/MAA molar ratios (0, 1 : 8, 1 : 6, and 1 : 4) in the feed composition of the hydrogels were also applied to study the influence of the molecular imprinting technique on their binding properties. The hydrogels (0.4 mm thick) were synthesized by thermal polymerization at 60°C for 24 h in a polypropylene mold. The hydrogels were then characterized by the determination of their swelling and binding properties in water. Their loading and release properties were also studied in 0.9% NaCl and artificial lachrymal fluid. Increasing the MAA content of the hydrogel and applying the molecular imprinting technique led to an increase in the loading capacity of the hydrogel. The optimized imprinted hydrogel showed the highest affinity for PA and the greatest ability to control the release process, sustaining it for 48 h. The results obtained clearly indicate that the incorporation of MAA as a comonomer increased the PA loading capacity of hydrogel. Our data showed that the molecular imprinting technique also had a significant effect on the loading and release properties of the hydrogels. © 2012 Wiley Periodicals, Inc. J Appl Polym Sci, 2012