A nanocomposite of poly(N‐vinylcarbazole) with nanodimensional alumina

A nanocomposite of poly(N‐vinylcarbazole) (PNVC) and Al₂O₃ was prepared by precipitation of a preformed PNVC in a tetrahydrofuran solution onto an aqueous suspension of nanodimensional Al₂O₃. Prolonged extraction of a PNVC–Al₂O₃ composite by benzene failed to extract the loaded PNVC from the Al₂O₃, as shown by Fourier transform infrared studies. Scanning electron microscopy analyses revealed distinct morphological features of the composite, and transmission electron microscopy analyses confirmed that the particle sizes were in the range of 120–240 nm. Thermogravimetric analyses demonstrated the enhanced stability of the nanocomposite relative to the base polymer. Direct current conductivity of the PNVC–Al₂O₃ composites was found to be about 0.14 × 10^?6 S/cm. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 88: 2233–2237, 2003     

Synthesis of dendritic polyaniline nanofibers by using soft template of sodium alginate

Highly crystallized polyaniline (PANI) nanofibers were synthesized by oxidative polymerization of aniline in the presence of sodium alginate as a soft template in HCl and ammonium peroxydisulfate (APS) acting as an oxidizing agent. Sodium alginate, in presence of a protonic acid like HCl, formed hydrogen bonds with anilium ions or oligomers. The formed hydrogen bonds provide the driving force to form PANI nanofibers. The nanofibers were separated from the alginate gel by degelling with ammonium hydroxide and during degelling emeraldine salt was converted into emeraldine base form. The polymerized PANI was characterized using ultraviolet (UV)–visible spectroscopy, Fourier transform infrared spectroscopy (FTIR), X‐ray diffraction (XRD), and scanning electron microscopy (SEM). UV and FTIR spectra showed that the presence of sodium alginate had no effect on the electronic state and backbone structures of the resulting PANI products. It was evident from the XRD analysis that the obtained PANI nanofibers exhibit higher crystalline order. SEM micrographs showed that PANI nanofibers were just like a mat of interwoven twisted nanofibers. After magnification of the SEM image, it was found that most of the nanofibers were interconnected to form ramose structures rather than isolated nanofibers. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Biocompatible,stimuli‐responsive hydrogel of chemically crosslinked β‐cyclodextrin as amoxicillin carrier

A novel pH‐responsive, chemically crosslinked hydrogelator (cl‐β‐CD/pVP) has been fabricated using β‐cyclodextrin (β‐CD) and N‐vinyl pyrollidone (N‐VP) in presence of diurethane dimethacrylate (DUDMA) crosslinker/azobisisobutyronitrile initiator through free radical polymerization. Various grades of cl‐β‐CD/pVP have been synthesized and the best grade has been considered with higher crosslinking density, higher gel strength, and lower % swelling ratio. The hydrogelator has been characterized by FTIR, ¹H and ¹³C NMR spectroscopy, TGA, and FESEM analyses. The hydrogelator demonstrates pH‐responsive behavior, which has been confirmed by swelling behavior and gel characteristics at various pH (at 37 °C). Using hen egg lysozyme, degradation experiment has been performed, which confirms the biodegradable nature of the hydrogel. The in vitro cytotoxicity study and live–dead assay suggest that the hydrogelator is cytocompatible toward MG‐63 cells. Finally, the hydrogelator shows excellent efficacy as an antibiotic (amoxicillin) carrier. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 45939.     

Functionalization of styrene–butadiene rubber with meta‐pentadecenyl phenol for better processing: A multifunctional additive and renewable resource

Meta‐pentadecenyl phenol, a nonisoprenoid phenolic lipid, is a renewable agricultural resource and also a byproduct of the cashew industry; it is popularly known as cardanol. This study throws light on the grafting of cardanol, which has been established as a multifunctional additive for natural rubber, onto the main‐chain backbone of styrene–butadiene rubber (SBR), a synthetic polymer used to imbibe the multifunctional properties of the former, such as those of a plasticizer, curing promoter, process aid, and antioxidant, into the latter. The grafting was carried out in the solution stage on a trial basis with a peroxide catalyst, and all of the grafting parameters were optimized with a Taguchi methodology. The grafting of cardanol onto the SBR backbone was successfully confirmed by UV–visible spectroscopy, Fourier transform infrared spectroscopy, and NMR analysis. Thermal analysis of the cardanol‐grafted styrene–butadiene rubber (C‐g‐SBR) revealed a higher thermal stability and better plasticizing effect than that those found in the virgin SBR. The rheological properties of the grafted rubber indicated the improvement of the pseudo‐plastic (shear‐thinning) nature compared to that in gum SBR. The unfilled C‐g‐SBR vulcanizates exhibited physicomechanical properties comparable to 5‐phr processing‐oil‐containing SBR [oil‐plasticized styrene–butadiene rubber (OPSBR)] vulcanizates. The carbon‐black‐filled C‐g‐SBR vulcanizates exhibited improved plasticization, a faster curing rate, easy processability, and better physicomechanical properties compared to the 5‐phr OPSBR vulcanizates. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 45150.     

Speciality polymer blends of polyurethane elastomers and chlorinated polyethylene rubber (peroxide cure)

Two elastomers having polar reactive functional groups may react with each other upon heating. Considering this view, blends of polyurethane (AU) and chlorinated polyethylene (CPE) elastomer have been prepared where better performance properties can be obtained through interchain crosslinking reaction. The entire study was carried out using dicumyl peroxide (DCP) as a curing agent where both the phases were vulcanized to form new materials. The state of cure gradually increased with the addition of CPE. Hardness, modulus and tensile strength were also increased with increase of CPE content. The elongation at break decreased with higher amount of CPE. After ageing, hardness increased but the modulus and tensile strength decreased. There was drastic change in elongation at break on ageing. IR spectra suggested that interchain crosslinking occurred between AU and CPE elastomers. High temperature DSC studies also revealed the improvement of thermal stability with the addition of CPE. SEM study also suggested interphase crosslinking. © 2000 Society of Chemical Industry     

The bulk polymerisation of N-vinylcarbazole in the presence of both multi- and single-walled carbon nanotubes: A comparative study

The bulk polymerisation of N-vinylcarbazole (NVC) at an elevated temperature in the presence of both multi- and single-walled carbon nanotubes (CNTs) leads to the formation of two different types of composite materials, the morphology and properties of which were characterised by a field emission scanning electron microscopy (FE-SEM), Fourier transform infrared (FTIR) spectroscopy, Raman spectroscopy, X-ray photoelectron spectroscopy (XPS), thermogravimetric analysis, and electrical property measurements. The efficiency of CNTs to initiate the NVC polymerisation was investigated using both multi-walled CNTs (MWCNTs) and single-walled CNTs (SWCNTs). The focus was on three major aspects: the degree of polymerisation, the morphology and the properties of the resulting nanocomposite materials. Results showed that SWCNTs were more efficient in initiating NVC polymerisation than MWCNTs, and the morphology of resultant nanocomposites revealed wrapping and grafting of some poly(N-vinylcarbazole) (PNVC) chains on the SWCNT surfaces. The morphology of the PNVC/MWCNT nanocomposites showed only homogeneous wrapping of the outer surfaces of MWCNTs by PNVC chains. The direct current (dc) electrical conductivity of pure PNVC improved dramatically in the presence of both MWCNTs and SWCNTs, however, the extent of improvement is higher in the case of PNVC/MWCNT nanocomposites.     

Synthesis of Co3O4/Poly(N‐vinylcarbazole) Core/Shell Composite With Enhanced Optical Property

Co₃O₄/poly(N‐vinylcarbazole) (PNVC) composite with enhanced optical property was synthesized via a simple in situ bulk polymerization of NVC monomers in the presence of Co₃O₄ nanoparticles at an elevated temperature. High‐resolution electron microscopic observations showed that the Co₃O₄ nanoparticles were coated with uniform nanolayer shells of PNVC. Fourier‐transform infrared (FT‐IR) spectroscopy revealed the presence of strong interactions between the PNVC polymer chains with the Co₃O₄ surface in the Co₃O₄/PNVC composite. Raman spectroscopic results supported conclusions based on electron microscopy and FT‐IR spectra. The uniform nanolayer coating of PNVC decreases the inherent bulk conductivity of Co₃O₄, however, significantly increases the fluorescence property of Co₃O₄ nanoparticles.

     

Microstructures,Martensitic Transformation,and Mechanical Behavior of Rapidly Solidified Ti-Ni-Hf and Ti-Ni-Si Shape Memory Alloys

In this work, the microstructure and mechanical properties of rapidly solidified Ti_50?x/2Ni_50?x/2Hf _x (x = 0, 2, 4, 6, 8, 10, and 12 at.%) and Ti_50?y/2Ni_50?y/2Si _y (y = 1, 2, 3, 5, 7, and 10 at.%) shape memory alloys (SMAs) were investigated. The sequence of the phase formation and transformations in dependence on the chemical composition is established. Rapidly solidified Ti-Ni-Hf or Ti-Ni-Si SMAs are found to show relatively high yield strength and large ductility for specific Hf or Si concentrations, which is due to the gradual disappearance of the phase transformation from austenite to twinned martensite and the predominance of the phase transformation from twinned martensite to detwinned martensite during deformation as well as to the refinement of dendrites and the precipitation of brittle intermetallic compounds.     

Role of the CCAAT-binding protein CBF/NF-Y in transcription

The CCAAT motif is one of the common promoter elements present in the proximal promoter of numerous mammalian genes transcribed by RNA polymerase II. CBF (also called NF-Y and CP1) consists of three different subunits and interacts specifically with the CCAAT motif. In each CBF subunit, the segment needed for formation of the CBF-DNA complex is conserved from yeast to human and, interestingly, the conserved segment of two CBF subunits, CBF-A and CBF-C, are homologous to the histone-fold motif of eukaryotic histones and archaebacterial histone-like protein HMf-2. The histone fold motifs of CBF-A and CBF-C interact with each other to form a heterodimer that associates with CBF-B to form a heterotrimeric CBF molecule, which then binds to DNA.