Ionic Aggregates in Zn- and Na-neutralized Poly(ethylene-\u3cem\u3eran\u3c/em\u3e-methacrylic acid)

The morphology of ionic aggregates in semi-crystalline Zn- and Na-neutralized poly(ethylene-ran-methacrylic acid) (EMAA) ionomer blown films has been explored with scanning transmission electron microscopy (STEM) and small angle x-ray scattering (SAXS). The ionic aggregates of Zn-EMAA are spherical, monodisperse and uniformly-distributed in as-extruded pellets and blown films prepared at low and high blow-up ratio. Thus, although the biaxial stresses of film blowing are sufficient to alter the PE superstructure, the ionic aggregates in Zn-EMAA are unaffected. In contrast, the morphology of Na-EMAA as detected by STEM changes from featureless in the as-extruded pellets to a heterogeneous distribution of Na-rich aggregates in the blown films. This transformation in Na-EMAA morphology is consistent with our earlier study of quiescent annealing suggesting that the morphological change is the result of thermal processing rather than the biaxial stresses of film blowing

A Coagulation Method to Prepare Single-Walled Carbon Nanotube/PMMA Composites and Their Modulus, Electrical Conductivity, and Thermal Stability

A coagulation method that provides better dispersion of SWNT in the polymer matrix has been used to produce single-walled carbon nanotube (SWNT)/poly(methyl methacrylate) (PMMA) composites. Optical microscopy and SEM show improved dispersion of SWNT in the PMMA matrix, which is a key factor in composite performance. Aligned and unaligned composites were made with purified SWNT with different SWNT loadings, from 0.1 to 7 wt%. Comprehensive testing shows improved elastic modulus, electrical conductivity, and thermal stability with addition of SWNT. The electrical conductivity of a 2 wt% SWNT composite decreases significantly (\u3e105), when the SWNT is aligned and this result is discussed in terms of percolation

Effect of nanotube alignment on percolation conductivity in carbon nanotube/polymer composites

Percolation conductivity of a stick network depends on alignment as well as concentration. We show that both dependences exhibit critical (power-law) behavior, and study the alignment threshold in detail. The highest conductivity occurs for slightly aligned, rather than isotropic, sticks. Experiments on single wall carbon nanotube composites are supported by Monte Carlo simulations. These results should be broadly applicable to percolating networks of anisotropic conductors

Production of haloperidol loaded PLGA nanoparticles for extended controlled drug release of haloperidol

This study developed an emulsion-solvent evaporation method for producing haloperidol-loaded PLGA nanoparticles with up to 2% (wt/wt. of polymer) drug content, in vitro release duration of over 13 days and less than 20% burst release. The free haloperidol is removed from the nanoparticle suspension using a novel solid phase extraction technique. This leads to a more accurate determination of drug incorporation efficiency than the typical washing methods. It was discovered that PLGA end groups have a strong influence on haloperidol incorporation efficiency and its release from PLGA nanoparticles. The hydroxyl-terminated PLGA (uncapped) nanoparticles have a drug incorporation efficiency of more than 30% as compared to only 10% with methyl-terminated PLGA (capped) nanoparticles. The in vitro release profile of nanoparticles with uncapped PLGA has a longer release period and a lower initial burst as compared to capped PLGA. By varying other processing and materials parameters, the size, haloperidol incorporation and haloperidol release of the haloperidol-loaded PLGA nanoparticles were controlled

Controlling the \u3cem\u3eIn Vitro\u3c/em\u3e Release Profiles for a System of Haloperidol-Loaded PLGA

We have used a systematic methodology to tailor the in vitro drug release profiles for a system of PLGA/PLA nanoparticles encapsulating a hydrophobic drug, haloperidol. We applied our previously developed sonication and homogenization methods to produce haloperidol-loaded PLGA/PLA nanoparticles with 200–1000 nm diameters and 0.2–2.5% drug content. The three important properties affecting release behavior were identified as: polymer hydrophobicity, particle size and particle coating. Increasing the polymer hydrophobicity reduces the initial burst and extends the period of release. Increasing the particle size reduces the initial burst and increases the rate of release. It was also shown that coating the particles with chitosan significantly reduces the initial burst without affecting other parts of the release profile. Various combinations of the above three properties were used to achieve in vitro release of drug over a period of 8, 25 and \u3e40 days, with initial burst \u3c25% and a steady release rate over the entire period of release. Polymer molecular weight and particle drug content were inconsequential for drug release in this system. Experimental in vitro drug release data were fitted with available mathematical models in literature to establish that the mechanism of drug release is predominantly diffusion controlled. The average value of drug diffusivities for PLGA and PLA nanoparticles was calculated and its variation with particle size was established

Increased Flexural Modulus and Strength in SWNT / Epoxy Composites by a New Fabrication Method

A new method for preparing SWNT/epoxy nanocomposites has been developed which involves high shear mixing of the epoxy resin and SWNT and heat treating the mixture prior to introducing the hardener. The glass transition temperature of the epoxy resin is unaffected by the presence of nanotubes. An improvement of 17% in flexural modulus and 10% in flexural strength has been achieved at 0.05 wt% of nanotubes. These improvements in flexural modulus and strength are attributed to good dispersion of the nanotubes and grafting of epoxy resin to SWNT by an esterification reaction

Interfacial in situ polymerization of single wall carbon nanotube/nylon 6,6 nanocomposites

An interfacial polymerization method for nylon 6,6 was adapted to produce nanocomposites with single wall carbon nanotubes (SWNT) via in situ polymerization. SWNT were incorporated in purified, functionalized or surfactant stabilized forms. The functionalization of SWNT was characterized by FTIR, Raman spectroscopy and TGA and the SWNT dispersion was characterized by optical microscopy before and after the in situ polymerization. SWNT functionalization and surfactant stabilization improved the nanotube dispersion in solvents but only functionalized SWNT showed a good dispersion in composites, whereas purified and surfactant stabilized SWNT resulted in poor dispersion and nanotube agglomeration. Weak shear flow induced SWNT flocculation in these nanocomposites. The electrical and mechanical properties of the SWNT/nylon nanocomposites are briefly discussed in terms of SWNT loading, dispersion, length and type of functionalization

Cellular Structures of Carbon Nanotubes in a Polymer Matrix Improve Properties Relative to Composites with Dispersed Nanotubes

A new processing method has been developed to combine a polymer and single wall carbon nanotubes (SWCNTs) to form electrically conductive composites with desirable rheological and mechanical properties. The process involves coating polystyrene (PS) pellets with SWCNTs and then hot pressing to make a contiguous, cellular SWCNT structure. By this method, the electrical percolation threshold decreases and the electrical conductivity increases significantly as compared to composites with a well-dispersed SWCNTs. For example, a SWCNT / PS composite with 0.5 wt% nanotubes and made by this coated particle process (CPP) has an electrical conductivity of ~ 3 x 10-4 S/cm, while a well-dispersed composite made by a coagulation method with the same SWCNT amount has an electrical conductivity of only ~ 10-8 S/cm. The rheological properties of the composite with a macroscopic cellular SWCNT structure are comparable to PS, while the well-dispersed composite exhibits a solid-like behavior, indicating that composites made by this new CPP method are more processable. In addition, the mechanical properties of the CPP-made composite decrease only slightly, as compared with PS. Relative to the common appoach of seeking better dispersion, this new fabrication method provides an important alternative means to higher electrical conductivity in SWCNT / polymer composites. Our straightforward particle coating and pressing method avoids organic solvents and is suitable for large-scale, inexpensive processing using a wide variety of polymer and nanoparticles

Temperature Dependence of Thermal Conductivity Enhancement in Single-walled Carbon Nanotube/polystyrene Composites

The thermal conductivity of single-walled carbon nanotube (SWCNT)/polystyrene composites, prepared by a method known to produce a uniform distribution of SWCNT bundles on the micrometer length scale, was measured in the temperature range from approximately 140 to 360 K. The thermal conductivity enhancement (50% for 1 mass % at 300 K) is reasonably constant above room temperature but is reduced at the lower temperatures. This result is consistent with the expected, large contribution of interfacial thermal resistance in SWCNT/polymer composites. Enhancements in electrical conductivity show that 1 mass % loading is in the region of the electrical percolation threshold

Simulations and Generalized Model of the Effect of Filler Size Dispersity on Electrical Percolation in Rod Networks

We present a three-dimensional simulation of electrical conductivity in isotropic, polydisperse rod networks from which we determine the percolation threshold (ϕc). Existing analytical models that account for size dispersity are formulated in the slender-rod limit and are less accurate for predicting ϕc in composites with rods of modest L/D. Using empirical approximations from our simulation data, we generalized the excluded volume percolation model to account for both finite L/D and size dispersity, providing a solution for ϕc of polydisperse rod networks that is quantitatively accurate across the entire L/D range