Recycling of silicone rubber waste: Effect of ground silicone rubber vulcanizate powder on the properties of silicone rubber

The silicone rubber vulcanizate powder (SVP) obtained from silicone rubber by mechanical grinding exists in a highly aggregated state. The particle size distribution of SVP is broad, ranging from 2 µm to 110 µm with an average particle size of 33 µm. X‐ray Photoelectron Spectroscopy (XPS) and Infrared (IR) Spectroscopy studies show that there is no chemical change on the rubber surface following mechanical grinding of the heat‐aged (200°C/10 days) silicone rubber vulcanizate. Addition of SVP in silicone rubber increases the Mooney viscosity, Mooney scorch time, shear viscosity and activation energy for viscous flow. Measurement of curing characteristics reveals that incorporation of SVP into the virgin silicone rubber causes an increase in minimum torque, but marginal decrease in maximum torque and rate constant of curing. However, the activation energy of curing shows an increasing trend with increasing loading of SVP. Expectedly, incorporation of SVP does not alter the glass‐rubber transition and cold crystallization temperatures of silicone rubber, as observed in the dynamic mechanical spectra. It is further observed that on incorporation of even a high loading of SVP (i.e., 60 phr), the tensile and tear strength of the silicone rubber are decreased by only about 20%, and modulus dropped by 15%, while the hardness, tension set and hysteresis loss undergo marginal changes and compression stress‐relaxation is not significantly changed. Atomic Force Microscopy studies reveal that incorporation of SVP into silicone rubber does not cause significant changes in the surface morphology.     

Conducting blends of poly(o‐toluidine) and ethylene–propylene–diene terpolymer

Poly(o‐toluidine) (POT) is an electroactive polymer with poor mechanical and thermal characteristics. We examined the scope for improving such properties by making blends of POT with ethylene–propylene–diene rubber (EPDM). We prepared POT–EPDM blends containing different weight fractions of POT by intimately mixing known volumes of separate solutions of the two polymers (POT in THF and EPDM in toluene). Films of EPDM and POT–EPDM blends in solution were obtained by spreading, solvent evaporation, and film casting techniques. POT, EPDM, and their blends were characterized in solution by ultraviolet‐visible spectroscopy, and the respective dried samples were analyzed by Fourier transform infrared spectroscopy and thermogravimetry. The polymer samples were further analyzed morphologically by scanning electron microscopy, and their tensile strengths were also evaluated. Spectroscopic and thermal studies of the blends indicated some sort of interaction between the two constituent polymers. The direct current electrical conductivity of the blends in increasing order of POT loading (12.5–100%) was in the range 9.9 × 10^?5 to 11.6 × 10^?2 S cm^?1. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 88: 2550–2555, 2003     

Recent advances on injectable nanocomposite hydrogels towards bone tissue rehabilitation

There has been significant interest in the recent past to develop injectable hydrogel scaffolds that follow minimally invasive implantation procedures towards efficient healing and regeneration of defective bone tissues. Such scaffolds offer several advantages, as they can be injected into the irregularly shaped defect and can act as a low-density aqueous reservoir, incorporating necessary components for bone tissue repair and augmentation. Considering that bone is a biocomposite of natural biopolymer and bioapatite nanofiller, there has been a growing trend to develop nanocomposite scaffolds by combining biopolymers and inorganic nanofillers to biomimic the hierarchical nanostructure and composition of natural bone. Furthermore, the nanocomposite scaffolds can be tailored to have patient-specific bone properties, which can lead to better biological responses. The present article begins with the introduction, followed by an overview of polymer matrices, property requirements, and crosslinking techniques employed for injectable hydrogels. Various strategies to develop injectable composites, with emphasis on nanocomposite hydrogels incorporating bioinert and bioactive nanofillers have been discussed. The fundamental challenges related to the development of injectable hydrogel nanocomposite scaffolds and the research efforts directed towards solving these problems have also been reviewed. Finally, future trends and conclusions on new generation injectable hydrogel nanocomposite bone scaffolds have been discussed in this article.     

Affinity Studies of Hemicyanine Derived Water Soluble Colorimetric Probes with Reactive Oxygen/Nitrogen/Sulfur Species

Peroxynitrite (ONOO^-) is an essential endogenous reactive oxygen species (ROS) generated in mitochondria under various pathological and physiological conditions. An increase in its level in mitochondria is related to numerous diseases. Herein, we report a series of hemicyanine-derived water-soluble colorimetric probes ( 1 – 4 ) and the reactivity of which was studied with various reactive oxygen, nitrogen, and sulfur species. Probes 1 – 4 are formed by conjugating 1,2,3,3-tetramethyl-3H-indolium iodide and 4-hydroxybenzaldehyde or its derivatives through an alkene linkage formed by the Knoevenagel reaction. Oxidative cleavage of the electron-rich double bond of the conjugated hemicyanine dye revealed a discerning affinity of probe 3 towards peroxynitrite among all reactive oxygen species. The rapid change in color of 3 provides a sensitive and selective method for detecting peroxynitrite with a low detection limit of 180 nM. Notably, the water solubility of the probe displays excellent performance for the selective detection of peroxynitrite among ROS and reactive nitrogen (RNS)/sulfur species (RSS). UV-vis, ¹H NMR, and ¹³C NMR spectroscopic data and results from theoretical calculations provide further information on the interaction of peroxynitrite with probe 3 .     

Peracetic acid bleaching of banana fibre: Process optimisation

Banana is an important commercially available natural fibre, suitable for making coarse yarns. It has also potential for making fine home and apparel textiles after requisite chemical intervention or blending with other fine fibres. For making such products, chemical processing, namely bleaching, coloration and finishing, play an important role. Bleaching of fibre is generally carried out in highly alkaline condition and at high temperature of 85°C using hydrogen peroxide to achieve whiteness index of > 70 with about 25% loss in tensile strength. To achieve a similar whiteness index, while addressing strength loss, a fibre friendly low-temperature low-alkali based peracetic acid (PAA) bleaching of banana fibre has been proposed in the present article. Important bleaching process parameters, namely PAA concentration (10–30 g/L), time (60–180 min) and temperature (60–80°C), have been varied for optimisation of the bleaching process. Banana fibre bleaching using PAA concentration of 20 g/L at 70°C for 2 h can produce fibre with whiteness index of > 70, which is suitable for subsequent coloration. The PAA bleached banana fibre can retain 84% of its bundle strength and 95.6% of its weight. Physical (strength, fineness), chemical (attenuated total reflectance Fourier-transform infrared [ATR-FTIR], energy dispersive X-ray spectroscopy [EDX]), optical (colour) and morphological (scanning electron microscopy [SEM]) properties of banana fibres before and after bleaching were evaluated to study the efficacy of the process.     

Synthesis of Red-Light-Responsive Pheophorbide-a Tryptamine Conjugated Photosensitizers for Photodynamic Therapy

Six methyl pheophorbide-a derivatives were prepared by linking a tryptamine side chain at the C-13 ¹ , C-15 ² and C-17 ³ positions of pheophorbide-a. P repared conjugates were characterized and evaluated for their photocytotoxicity against A549 cells. The conjugate 6 a with strong absorption at 413 nm (Soret band), 663–671 nm (Q bands) and comparable fluorescence quantum yield (0.26) was found to exhibit significant cytotoxicity (659 nM). Molecular integration of pheophorbide-a and tryptamines showed synergistic effects as the most potent conjugate 6 a was identified with enhanced photocytotoxicity when compared to methyl pheophorbide-a. T he conjugate 6 a was smoothly taken up by A549 cells and exhibited intracellular localization predominantly to lysosome in the cytoplasm. Upon photoirradiation 6 a generated singlet oxygen to show potent cytotoxicity toward A549 cells.     

Effect of functionalization on dispersion of POSS‐silicone rubber nanocomposites

The nanocomposite of PDMS using functionalized fumed silica and nonreactive POSS as fillers were prepared by blend method in a planetary mixer. Fumed silica was functionalized by aliphatic and aromatic groups to study the filler–filler interactions with the aliphatic and aromatic POSS fillers and consequently their influence on the properties in the PDMS matrix. Transmission electron microscope (TEM) showed a good dispersion in the systems having the silica and POSS fillers with similar modifications. However, aliphatic and aromatic filler combinations showed more aggregated structures. Moreover, aliphatic POSS despite of good dispersion at higher loadings, act as lubricant, which is attributed to the disturbance in the PDMS‐ silica filler interaction and also the filler–filler interaction within fumed silica. There is a decrease in complex viscosity with the functionalization of fumed silica and with the aromatic/aliphatic POSS fillers. The thermal stability of aromatic functionalized fillers improves owing to the thermally stable phenyl groups. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Preparation and characterization of polypyrrole/modified multiwalled carbon nanotube nanocomposites polymerized in situ in the presence of barium titanate

Polypyrrole (PPy) composites were prepared with both unmodified and amine‐modified multiwalled carbon nanotubes (MWCNTs) in the presence and absence of barium titanate (BaTiO₃) by in situ oxidative polymerization. A uniform coating of PPy on the MWCNTs and BaTiO₃ surfaces was confirmed by field emission scanning electron microscopy and high‐resolution transmission electron microscopy images. The structure of the pure and amine‐modified MWCNTs were identified by Fourier transform infrared spectroscopy. The incorporation of BaTiO₃ enhanced the thermal stability and capacitance properties of the composites. The maximum specific capacitance and energy density values found for the PPy/amine‐modified MWCNT/BaTiO₃ composites were 155.5 F/g and 21.6 W h/kg, respectively, at a scan rate of 10 mV/s. The maximum power density was found to be 385.7 W/kg for the same composite at a scan rate of 200 mV/s. Furthermore, the impedance spectra of the composites showed moderate capacitive behavior. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Solvothermal Conversion of Nanofiber to Nanorod‐Like Mesoporous γ‐Al2O3 Powders,and Study Their Adsorption Efficiency for Congo Red

Mesoporous γ‐Al₂O₃ powders with nanofiber and nanorod‐like structures were synthesized using boehmite sols in the presence of triblock copolymer, P123 in ethanol by solvothermal process at different temparatures (100°C–165°C) followed by calcination at 400°C–1000°C. The powders were characterized by low‐ and wide‐angle X‐ray diffraction (XRD), N₂ adsorption–desorption, and transmission electron microscopy (TEM). The adsorption efficiency of the powders with Congo red (CR) was studied by UV–vis spectroscopy. The γ‐Al₂O₃ phase became stable up to 1000°C. The nanorods obtained at 165°C had narrower pore size distribution (PSD) than nanofibers synthesized at 100°C, the former showed higher CR adsorption efficiency. The stepwise growth mechanism of nanofibers to nanorods conversion with increase in solvothermal temperatures was illustrated.     

Environmental tobacco smoke removal capability of activated carbon

Removal of gaseous and vapor constituents of environmental tobacco smoke (ETS) by activated carbons in a packed bed arrangement was studied under dynamic conditions and was compared with that by silica gel and molecular sieve 13X. ETS is a mixture of sidestream smoke and exhaled mainstream smoke, and it consists of various organic and inorganic compounds, trace heavy metals, and particulate matters. Due to the complex nature of ETS-air mixture, its removal from indoors is a challenging task. For experimentation in a laboratory, the ETS was produced from a specially designed smoking apparatus that simulated the puffng of a cigarette by a person. Air containing ETS was passed through a bed containing about 25 grams of activated carbon at room temperature. The flow rate of air-ETS mixture through the bed was 4000 cm3/min. The relative humidity of the air was 50% and contained about 35 to 40 ppm of hydrocarbons as measured as methane-equivalent. The number of particles in the inlet air stream were in the range of 30,000 to 35,000 particles/cm3. About 60% of hydrocarbons present in ETS were removed at these operating conditions for a period of about 70 hours. Based on 15 adsorption and regeneration cycles, it was noted that the carbon bed did not loose its capacity for ETS significantly as indicated by the BET surface area and water adsorption data. At the beginning of an adsorption cycle, the carbon bed captured a significant number of particles. However, the bed rapidly lost its particle capture effciency as the experiment progressed. The number of particles in the outlet air stream was found to be the same as that of the inlet stream within five minutes.