Narrow Results

UV embossing for polymeric micro-patterning thin film is an emerging replication technique. This paper investigates UV curable multifunctional acrylates pre-polymer resin patterned by a micro-structured mold and subsequently cured by UV irradiation. To further enhance this duplication method for high aspect ratio production, demolding must be reliable and repeatable without damage to the embossing or mold. Previously, it has been reported that UV embossed patterns for aspect ratios as high as 14 have been achieved experimentally. Finite element analyses for patterns with aspect ratios of 5 using parallel demolding between two parallel plates have also been reported. However, the parallel demolding method may not be suitable for large area patterns as forces generated were high. As such, an alternative demolding method, namely peel demolding, for micro-patterns with an aspect ratio of 14 was investigated and key parameters identified. The parameters governing the demolding process were the peel angle, the pre-crack condition, shrinkage, interface fracture toughness, tensile strength and modulus of polymer. A pre-crack between the polymer and mold was introduced before peel demolding. Numerical analyses in terms of Cohesive Zone Modeling (CZM) were used to simulate the demolding process. Shrinkage caused by UV exposure was represented by thermal strain effects and the fully cured polymer was peeled off using displacement control. The ultimate tensile strength (U.T.S) of the cured polymer was used as a failure criterion. The stresses involved were crucial for determining clean demolding. As peeling progressed, stresses experienced in the polymer matrix increased rapidly in the region ahead of the crack with little or no stress at the cracked region. When stresses experienced by the polymer were below the U.T.S, demolding was deemed to be successful.

Electrospinning is a very simple and versatile process by which polymer nanofibers with diameters ranging from a few nanometers to several micrometers can be produced using an electrostatically driven jet of polymer solution (or polymer melt). Significant progress has been made in this process throughout the last decade and the resultant nanostructures have been exploited to a wide range of applications. An important feature of the electrospinning process is that electrospinning nanofibers are produced in atmospheric air and at room temperature. This paper reviews the assembled polyacrylonitrile (PAN)-based carbon nanofibers with various processing parameters such as electrical potential, distance between capillary and collector drum, solution flow rate (dope extrusion rate), and concentration of polymer solution. The average fiber diameter would increase with increasing concentration of the polymer solution and the flow rate. Therefore, the screen distance could also increase but the average electrical potential of the fibers diameter decreases. Electrospinning process can be conducted at higher electrical potentials, lower flow rate, nearer screen distance, and higher concentrations of dope.

One of the most important techniques to improve the functional properties of organized molecular films is to introduce nanometer-size solid particles into them. The Langmuir balance has proved to be useful for controlling and modifying these films by organizing molecules into highly ordered structures. Our aim is to study the efficacy of this technique to improve the compactness of biocompatible polymer films by incorporating nanosilica particles. The experimental technique consists of first adsorbing the polymer on silica particles in an aqueous medium, followed by preparation of a monolayer at the air–water interface in a Langmuir balance. The film is organized by repeated expansion and compression. The surface pressure-surface area characteristics are recorded during each cycle. The pressure of the film increases with decrease in the mean molecular area, but reaches a plateau, probably due to instability of the film. With repeated cycling, the plateau pressure increases indicating that the film has become more stable and rigid. The cycling is continued till plateau pressure does not change with further cycling. The amount of the polymer loaded on the subphase and the ratio of PEO to silica in the film, on the plateau pressure has been studied. A substantial increase in the stability and rigidity of the film is achieved by this technique.

In this project, nanocomposite films were prepared with different Titanium dioxide (TiO₂) percentages. Properties of polycarbonate (PC) and PC–TiO₂ nanocomposite films were studied by X-ray diffraction (XRD) analysis and Fourier transform infrared (FTIR) spectroscopy. The structure of samples was studied by XRD. The mechanical properties of PC–TiO₂ nanocomposite films were investigated by conducting tensile tests and hardness measurements. Thermal stability of the nanocomposites was studied by thermogravimetric analysis (TGA) method. The elastic modulus of the composite increased with increasing weight fraction of nanoparticles. The microhardness value increases with increasing TiO₂ nanoparticles. The results of tensile testing were in agreement with those of micro-hardness measurements. In addition, TGA curves showed that nanocomposite films have higher resistance to thermal degradation compared to polycarbonate. There are many reports related to the modification of polycarbonate films, but still a systematic study of them is required.

This research aims to study the addition of nanoclays on unsaturated polyester (UP) and epoxy resin (EP) as filling and by weight percentage (2%, 4% and 6%) to this mixture and then study the extent of the effect of this addition on wear rate of the composites’ material where three loads were adopted (10, 15 and 20N), respectively, on the iron hard disk (269 HB) and copper hard disk of 111HB for the resin before and after adding the clays, where the approved sliding velocities were 4.1887, 3.1415 and 2.0943m/sec, respectively, and the test duration was 10 min on the test disc. Immersion of samples in the water for 2, 4, 6 and 8 weeks showed a clear improvement in the wear rate and tear values of dry and submerged conditions in a water under different conditions of load change, slipping speed, time and temperature stability after adding the nanoclays to the polymer.

In recent times, nanomaterials have attracted the interest of the scientific community with their superior applications when compared to bulk counterparts. Tungsten oxide (WO₃) nanoparticles (NPs) with their distinct properties such as electrochemical, photocatalytic, photoluminescent and gas sensing capabilities, are highly sought out. With these distinct properties, WO₃ NPs find significant application in device fabrication. This review provides an overview of the different synthesis methods, the properties and applications of tungsten oxide and doped tungsten oxide. The enhanced properties of WO₃ NPs with doping are also discussed in detail. In addition, this review also emphasizes on properties of WO₃ polymer nanocomposite and their applications in several areas of human enterprise.

Polymer nanocomposites (PNCs) are functional hybrids lying at the interface of organic and inorganic realm, whose high versatility offers numerous possibilities to develop tailor-made materials with advanced material behaviors. Accordingly, a considerate combination of optically effective additive and particle-stabilizing polymer often opens up unique design possibilities, thereby offering momentous lead in creating advanced functional materials for targeted techno-commercial applications. Accordingly, optically effective nanofillers characterized by particle size and dielectric constant of the surrounding medium-dependent surface plasmon resonance effects may induce entirely new optical functionalities (UV and visible light absorption, optical dichroism, spectral manipulation, photonic emission and so forth) in the polymeric host. Herein, we discuss the major causative factors, which enable nanostructured materials to exhibit unique properties, general introduction to nanotechnology-enabled polymer-based nanocomposites and present a comprehensive review on functional properties and related applications of PNCs, with special emphasis on optical functionalities (photonic absorption encompassing UV shielding, color switching and refractive index engineering and photonic emission covering photoluminescence and spectral manipulations). This review also sheds light on the effect of nature of filler, filler morphology, filler size and filler composition and dispersion homogeneity on optical behaviors of polymer nanocomposites.

It is shown that the molecules of double — stranded DNA form a liquid-crystaline ordered phase, depending on the value of parameter of Flory-Huggins, DNA aspect ratio, energy of attraction between the molecules of DNA and volume fraction of the flexible polymer. Liquid crystalline order formation in double-stranded DNA, immeresed in the polymeric matrix occurs with increase of the volume fraction of the flexible polymer. The orrdered phase formation in double-stranded DNA is governed by volume fraction of DNA and by temperature. The results clearly show the effect of the polymer matrix on the ordering in DNA molecules.

Cadmium sulphide (CdS) nanocrystallites were prepared by sulphuration route with capping in polyethylene oxide (PEO) polymer matrix. It is found that PEO could provide a confined environment for particle nucleation and growth of CdS nanocrystallites. The scanning electron microscopy (SEM) with energy dispersive analysis by X-ray (EDAX) studies confirms the presence of CdS nanocrystallites in polymer matrix. X-ray diffraction (XRD) studies and transmission electron microscopy (TEM) selected area diffraction (SAD) patterns show that these crystallites have hexagonal structure. The TEM and UV-Visible absorption studies indicate uniform size distribution having size around 2.3 nm and band gap of 2.7 eV. X-ray photoelectron spectroscopy (XPS) studies reveal that core level energy positions of the Cd is shifted towards the lower binding energy and has similar chemical environment to that of bulk CdS.

A novel and shape-controlled synthesis method for uniformly-shaped poly(p-phenylenediamine) (PpPD) microparticles was developed using (NH₄)₂S₂O₈ (APS) as an oxidant. The results demonstrated that the morphologies of PpPD varied from nanofibers to nanospheres and nest-like microspheres by tuning the pH of solution. Tiny pH change leads to the significant change in product morphology. The structure of microspheres is similar to graphene which was first discovered. Further study showed that the PpPD nanofibers were dimer. The difference in the structure of PpPD nanofibers and nanospheres (microspheres) resulted in different solubility in water. The nanosized oligomer crystallites served as starting templates for the nucleation of PpPD nanofibers. Further growth of nanofibers was proceeded by the self-organization of phenazine units or their blocks located at the ends of the PpPD chains.

The electrochemical properties of poly sodium 4-styrenesulfonate intercalated graphite oxide (PSSGO) have been investigated in a 1 M H₂SO₄ electrolyte. We observed capacitor behavior at scan rate of 1–25 mV/s in a cyclic voltammetry. Specific capacitance obtained from galvanostatic charge and discharge measurements were 6 F/g to 102 F/g at 1 A/g to 0.1 A/g, respectively. The specific capacitance of PSSGO is relatively high compared to that of the precursor graphite oxide in which the specific capacitance was 11–20 F/g at 0.03 A/g. Capacitance retention was 73% after 3000 cycles, proving reliable cyclic stability up to 3000 cycles.

Amphiphilic polymer carriers (PEG–St–$R$) were prepared from cassava starch and their pH response was investigated. First, hydrophobic tapioca starch polymer (St–$R$) was prepared with octyl acyl as the hydrophobic group. The hydrophilic group polyethylene glycol (mPEG) was then introduced into the polymer by esterification to produce amphiphilic tapioca starch polymer (PEG–St–$R$). Its self-assembly behavior was characterized using fluorescent probes. The morphology of PEG–St–$R$ was investigated by transmission electron microscopy (TEM). Loading of the anti-cancer drug curcumin was used to assess the delivery and slow-release performance of the amphiphilic tapioca starch polymer. Cumulative drug release was explored at various pH conditions, with the greatest release from drug-loaded micelles being observed under acidic conditions and stable in a neutral environment. These results provide a theoretical basis for the preparation of pH-responsive nanomicelle carriers, and a platform for the preparation of novel amphiphilic starch-based polymers.

Long polymer chains that mainly exhibit thermoplastic properties are recognized to demonstrate excellent thermal and mechanical features at the molecular level. For the purpose of facilitating its study, we present the results of a coarse-grained Molecular Dynamics (MD) and Dissipative Particle Dynamics (DPD) simulations under the Canonical ensemble (NVT) conditions. For each simulation method, the structure, static and dynamic properties were analyzed, with particular emphasis on the influence of density and temperature on the equilibrium of the polymer. We find, after correcting the Soft Repulsive Potential (SRP) parameters used in DPD method, that both simulation methods describe the polymer physics with the same accuracy. This proves that the DPD method can simplify the polymer simulation and can reproduce with the same precision the equilibrium obtained in the MD simulation.

Devices such as solar and fuel cells have been studied for many decades and noticeable improvements have been achieved. This paper proposes a Micro Photosynthetic Power Cell (μPSC) as an alternative energy-harvesting device based on photosynthesis of blue-green algae. The effect of important biodesign parameters on the performance of the device, such as no-load performance and voltage–current (V–I) characteristics, were studied. Open-circuit voltage as high as 993 mV was measured while a peak power of 175.37 μW was obtained under an external load of 850 Ω. The proposed μPSC device could produce a power density of 36.23 μW/cm², voltage density of 80 mV/cm² and current density of 93.38 μA/cm² under test conditions.

Membrane technologies are essential for water treatment, bioprocessing and chemical manufacturing. Stimuli-responsive membranes respond to changes in feed conditions (e.g., temperature, pH) or external stimuli (e.g., magnetic field, light) with a change in performance parameters (permeability, selectivity). This enables new functionalities such as tunable performance, self-cleaning and smart-valve behavior. Polymer self-assembly is a crucial tool for manufacturing such membranes using scalable methods, enabling easier commercialization. This review surveys approaches to impart stimuli responsive behavior to membrane filters using polymer self-assembly.

Nowadays tools based on Scanning Probe Methods (SPM) have become indispensable in a wide range of applications such as cell imaging and spectroscopy, profilometry, or surface patterning on a nanometric scale. Common to all SPM techniques is a typically slow working speed which is one of their main drawbacks. The SPM speed barrier can be improved by operating a number of probes in parallel mode. A key element when developing probe array devices is a convenient read-out system for measurements of the probe deflection. Such a read-out should be sufficiently sensitive, resistant to the working environment, and compatible with the operation of large number of probes working in parallel. In terms of fabrication, the geometrical uniformity i.e. the realisation of large numbers of identical probes, is a major concern but also the material choice compatible with high sensitivity, the detection scheme and the working environment is a challenging issue. Examples of promising applications using parallel SPM are dip-pen-nanolithography, data storage, and parallel imaging.

Sensing is a basic ability of smart structures. Self-sensing involves the structural material sensing itself. No device incorporation is needed, thus resulting in cost reduction, durability enhancement, sensing volume increase and absence of mechanical property diminution. Carbon fiber renders electrical conductivity to a composite material. The effect of strain/damage on the electrical conductivity enables self-sensing. This review addresses self-sensing in structural composite materials that contain carbon fiber reinforcement. The composites include polymer–matrix composites with continuous carbon fiber rein-forcement (relevant to aircraft and other lightweight structures) and cement–matrix composites with short carbon fiber reinforcement (relevant to the civil infrastructure). The sensing mechanisms differ for these two types of composite materials, due to the difference in structures, which affects the electrical and electromechanical behaviors. For the polymer–matrix composites with continuous carbon fiber reinforcement, the longitudinal resistivity in the fiber direction decreases upon uniaxial tension, due to the fiber residual compressive stress reduction, while the through-thickness resistivity increases, due to the fiber waviness reduction; upon flexure, the tension surface resistance increases, because of the reduction in the current penetration from the surface, while the compression surface resistance decreases. These strain effects are reversible. The through-thickness resistance, oblique resistance and interlaminar interfacial resistivity increase irreversibly upon fiber fracture, delamination or subtle irreversible change in the microstructure. For the cement–matrix composites with short carbon fiber rein-forcement, the resistivity increases upon tension, due to the fiber–matrix interface weakening, and decreases upon compression; upon flexure, the tension surface resistance increases, while the compression surface resistance decreases. Strain and damage cause reversible and irreversible resistance changes, respectively. The incorporation of carbon nano-fiber or nanotube to these composites adds to the costs, while the sensing performance is improved marginally, if any. The self-sensing involves resistance or capacitance measurement. Strain and damage cause reversible and irreversible capacitance changes, respectively. The fringing electric field that bows out of the coplanar electrodes serves as a probe, with the capacitance decreased when the fringing field encounters an imperfection. For the cement-based materials, a conductive admixture is not required for capacitance-based self-sensing.

Immunotherapy has offered an alternative therapy method for cancer patients with metastatic tumors or who are not suitable for surgical resection. Different from traditional surgery, radiotherapy and chemotherapy, immunotherapy mainly restores the activity of the body’s own immune cells silenced in the tumor microenvironment to achieve anticancer therapy. Gene therapy which corrects abnormal expression of immune cells in tumor microenvironment by delivering exogenous genes to specific immune cells, is the most widely studied immunotherapy. Although most available gene delivery vectors are still viral vectors, the further application of viral vectors is still limited by the immunogenicity and mutagenesis. Based on this, cationic polymeric gene vectors with high flexibility, high feasibility, low cost and high safety have been widely used in gene delivery. The structural variability of polymers allows specific chemical modifications to be incorporated into polymer scaffolds to improve their physicochemical properties for more stable loading of genes or more targeted delivery to specific cells. In this review, we have summarized the structural characteristics and application potential in cancer immunotherapy of these polymeric gene vectors based on poly(L-lysine), poly(lactic-co-glycolic acid), polyethyleneimine, poly(amidoamine) and hydrogel system.