Influence of carbon nanofibers reinforcement on thermal and electrical behavior of polysulfone nanocomposites

Carbon nanofiber (CNF) based polysulfone (PSU) nanocomposites have been developed successfully by a innovative solution mixing technique to explore the effect of state of dispersion and wt% loading of CNFs on different properties of PSU. In order to enhance the interfacial adhesion between CNFs and PSU, CNFs were functionalized by air oxidation. Thermal properties were characterized by using thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC) and it was seen that thermal stability of PSU was increased with increase in CNFs loading. The state of dispersion of CNFs throughout the PSU matrix and PSU–CNFs interaction were confirmed using field emission scanning electron microscopy (FESEM) and high resolution transmission electron microscopy (HRTEM) study. The electrical properties of nanocomposites were studied from direct current (DC) and alternating current (AC) resistivity measurement. DC resistivity registered a very low percolation threshold in‐between 0.5–1 wt% of CNFs loading. DC resistivity of PSU was decreased by nine orders of magnitude with the addition of 1 wt% CNFs loading. Dielectric constant and dissipation factor of nanocomposites were significantly increased with increase in CNFs content in nanocomposites. The enhancement in these properties suggests a great potential application of the resulting nanocomposites as multifunctional materials in various electronics industries. POLYM. ENG. SCI., 2012. © 2012 Society of Plastics Engineers     

Electrochemical inspection of polypyrrole/chitosan/zinc oxide hybrid composites

Polymer nanocomposite composed of polypyrrole, chitosan, and zinc oxide nanoparticles has been synthesized and it has been evaluated for various electrochemical aspects of the current electrochemical industry. The polypyrrole (PPy) was synthesized by the chemical oxidative polymerization reaction by employing ammonium persulfate as oxidizing agent. Composites of polypyrrole/chitosan (PPy/Chy) and polypyrrole/chitosan/ZnO (PCZ) composites were synthesized by the solution blending method. Detailed structural, morphological, thermal characterization of PPy, PPy/Chy, and PCZ were performed to characterize the specific features of the systems. The composites exhibit better thermal stability and high surface area and the addition of ZnO nanoparticle increase the crystallinity of the composite. Electrochemical characterization of the ITO electrodes modified with PPy, PPy/Chy, and PCZ were performed using cyclic voltammetry, electrochemical impedance spectroscopy, and amperometry techniques. The present study highlights the role of a bio-compatible material with high surface area and conductive constituent for designing of various high performing electronic noninvasive sensors, biosensors, and so forth.     

Graphene: a versatile nanoplatform for biomedical applications

Graphene, with its excellent physical, chemical, and mechanical properties, holds tremendous potential for a wide variety of biomedical applications. As research on graphene-based nanomaterials is still at a nascent stage due to the short time span since its initial report in 2004, a focused review on this topic is timely and necessary. In this feature review, we first summarize the results from toxicity studies of graphene and its derivatives. Although literature reports have mixed findings, we emphasize that the key question is not how toxic graphene itself is, but how to modify and functionalize it and its derivatives so that they do not exhibit acute/chronic toxicity, can be cleared from the body over time, and thereby can be best used for biomedical applications. We then discuss in detail the exploration of graphene-based nanomaterials for tissue engineering, molecular imaging, and drug/gene delivery applications. The future of graphene-based nanomaterials in biomedicine looks brighter than ever, and it is expected that they will find a wide range of biomedical applications with future research effort and interdisciplinary collaboration.     

Surface modification of coir fibers. II. Cu(II)‐ IO initiated graft copolymerization of acrylonitrile onto chemically modified coir fibers

A study of the graft copolymerization of acrylonitrile (AN) onto chemically modified coir fibers was carried out using a CuSO₄ and NaIO₄ combination as the initiator in an aqueous medium in a temperature range of 50–70°C. The graft yield was influenced by the reaction time, temperature, concentration of CuSO₄, concentration of NaIO₄, and monomer concentration. Grafting was also carried out in the presence of inorganic salts and organic solvents. A combination of copper(II) and sodium periodate (Cu²⁺‐IO) in an aqueous medium with an IO concentration of 0.005 mol L^?1 and a Cu²⁺ concentration of 0.004 mol L^?1 produced optimum grafting. The chemically modified and AN grafted fibers were characterized by FTIR and scanning electron microscopy (SEM). The SEM studies revealed that grafting not only takes place on the surface of the fibers but also penetrates the fiber matrix. The tensile properties like the maximum stress at break and extension at break of untreated, chemically modified, and AN grafted coir fibers were evaluated and compared. The extent of absorption of water of untreated, chemically modified, and grafted coir fibers was determined. It was found that grafting of AN imparts hydrophobicity onto coir fibers. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 84: 75–82, 2002; DOI 10.1002/app.10221     

Voltammetric Response and Determination of an Anti-Inflammatory Drug at a Cationic Surfactant-Modified Glassy Carbon Electrode

Electrochemical oxidation of thiosalicylic acid in the presence of cationic surfactant, cetyl trimethylammonium bromide (CTAB), at a glassy carbon electrode was investigated. The electrochemical response of a modified sensor towards thiosalicylic acid determination was studied by the means of cyclic voltammetry, linear sweep voltammetry and differential pulse voltammetry (DPV). The liquid phase oxidation of thiosalicylic acid in the presence of CTAB leads to a notable enhancement in the peak current and a lowering of the peak potential. The electrochemical process was observed to be adsorption-controlled, irreversible and involves oxidation of one electron. Effects of anodic peak potential (E _p), anodic peak current (I _pa) and heterogeneous rate constant (k ⁰) were calculated. The linear response was obtained in the range of 1.0 µM–1.0 mM with a detection limit of 113 nM.     

Synthesis,Surface Properties and Effect of an Amino Acid Head Group of 11-(2-Methoxy-4-vinylphenoxy)undecanoicacid-Based Anionic Surfactants

Our present research describes the surface properties of three biobased anionic surfactant synthesized from vinylguaiacol and 11-bromo undecanoic acid. To further improve its hydrophobicity and bioavailability, amino acid head group incorporation was carried out. All these synthesized compounds were thoroughly characterized using NMR and mass spectroscopy. The performance properties such as foaming, wetting, emulsification value and calcium tolerance were evaluated. The studied surfactants possess excellent emulsion stability and moderate calcium tolerance as compared to commercially available surfactant sodium lauryl sulfate (SLS). The micelle formation and the thermodynamics involved at the air–water interface were estimated from surface tension measurements. These surfactants showed a higher tendency towards adsorption at the air–water interface than micellization. Dynamic light scattering and steady state fluorescence anisotropy study were carried out to shed light on the bulk micellization properties of the synthesized surfactant. Along with spherical micelles of <5 nm size, larger aggregates (35–84 nm) were observed with higher anisotropy values. FESEM images further confirmed the larger spherical micelles formed by these surfactants. The surfactants formed chiral aggregates above the critical micelle concentration as indicated by circular dichroism spectra. These surfactants may be suitable candidates for additives to detergents to improve their calcium tolerance especially in the case of hard water. Furthermore, a low foaming ability along with high emulsion stability may find these surfactants to be better replacement of the conventional surfactant used as emulsifiers in many industrial applications.     

An in-Depth Analysis of the Swelling,Mechanical, Electrical,and Drug Release Properties of Agar–Gelatin Co-Hydrogels

Agar–gelatin-based co-hydrogels were prepared with different compositions of the agar and the gelatin fractions. The intermolecular hydrogen bonding was higher in the co-hydrogels as compared to the gelatin hydrogel. Swelling studies indicated diffusion-mediated swelling. The electrical stability of the co-hydrogels was higher as compared to the gelatin hydrogel. Though the firmness of the co-hydrogels was higher, Weichert model of viscoelasticity indicated that the inherent mechanical stability of the gelatin hydrogel was superior. The release of ciprofloxacin hydrochloride was predominately Fickian diffusion-mediated. In gist, the co-hydrogels can be tried as polymeric constructs for controlled drug delivery applications.     

Insight on Castor Oil Based Polyurethane and Nanocomposites: Recent Trends and Development

Castor oil has gained momentous attention as a valuable bio-based monomer and a potential alternative to the current petrobased polyol for synthesizing polyurethane due to the presence of inherent hydroxyl group. In spite of its huge potentiality very little has been reviewed regarding the development of polyurethane from castor oil. This review thus highlights the recent trends and development in the field of polyurethane and its nanocomposite based on castor oil including its biodegradability and weatherability studies. Further, this review also provides an insight regarding the utilization of castor oil based polyurethane and its nanocomposite for coating application.     

Stearic Acid Modified Stearyl Alcohol Oleogel: Analysis of the Thermal,Mechanical and Drug Release Properties

The present study delineates the effect of stearic acid on the properties of stearyl alcohol oleogel. Herein, a series of oleogels were prepared by mixing different proportions of fatty alcohol (Stearyl alcohol; gelator) and fatty acid (stearic acid; co‐gelator). The characterization of the oleogels was done by thermal, macro‐scale stress relaxation, drug release, and antimicrobial studies. The oleogels were formed by the self‐assembly of stearyl alcohol/stearic acid. Thermal studies indicated that the stearic acid alters the crystal morphology, polymorphic transition and rate of crystallization of stearyl alcohol. The firmness of the oleogels with higher stearic proportion was better, which was due to the formation of a rigid network structure of stearyl alcohol in the presence of stearic acid. The release of ciprofloxacin hydrochloride, model drug, from the oleogels was better from the oleogels with higher stearic acid content. The release of the drug from the oleogels was Fickian diffusion‐mediated; except the oleogel with the highest stearic acid proportion. The antimicrobial study showed that the drug loaded oleogels were able to resist the growth of Escherichia coli, model microbe.     

Some Observations on the Dielectric and Conductivity Behavior of Nanocomposites of Polyaniline with Fe3O4 and CuFe2O4

Nanocomposites of polyaniline with iron oxide (PANI-Fe₃O₄) and copper ferrite (PANI-CuFe₂O₄) were prepared and characterized by FTIR, HRTEM, XRD and FESEM. HRTEM images reveals that the main size distributions are located in the range between 25–34 and 22–28 nm in case of PANI-CuFe₂O₄ and PANI-Fe₃O₄ nanocomposites, respectively. The dielectric constant value for PANI-Fe₃O₄ nanocomposites reaches a maximum value as high as ～7000 (10² Hz), while the same for PANI-CuFe₂O₄ composite attains a maximum value of ～2600 at 10² Hz. A quantitative estimation of the contribution of the grain boundary and resistance parameters has been attempted in terms of Maxwell-Wagner two-layered model.