Facile Synthesis and Characterization of Few-Layer Multifunctional Graphene from Sustainable Precursors by Controlled Pyrolysis, Understanding of the Graphitization Pathway, and Its Potential Application in Polymer Nanocomposites.

The key feature of the present work is the dexterous utilization of an apparently destructive process, pyrolysis, for the synthesis of the most esteemed nanomaterial, graphene. This work is an attempt to synthesize graphene from nonconventional sources such as tannic acid, alginic acid, and green tea by a controlled pyrolysis technique. The precursors used in this work are not petroleum-derived and hence are green.

Controlled Methodology for Development of a Polydimethylsiloxane-Polytetrafluoroethylene-Based Composite for Enhanced Chemical Resistance: A Structure-Property Relationship Study.

Polydimethylsiloxane (PDMS) polymers are highly appreciated materials that are broadly applied in several industries, from baby bottle nipples to rockets. Momentive researchers are continuously working to understand and expand the scope of PDMS-based materials. Fluorofunctional PDMS has helped the world to apply in specialty applications.

Selective Orientation of Needlelike Sepiolite Nanoclay in Polymer Blend for Controlled Properties.

Sepiolite nanoclay needles have been selectively localized either in the natural rubber (NR) phase or in the carboxylated nitrile rubber (XNBR) phase of the XNBR/NR (50/50) blend prepared by the solution casting method. In a systematic manner, the role of the difference value between the interaction parameter of individual blend components (NR or XNBR)/solvent and the interaction parameter of sepiolite nanoclay/solvent in selectively localizing the sepiolite nanoclay to the NR phase or the XNBR phase of the XNBR/NR (50/50) blend has been explored. A higher percentage of sepiolite nanoclay resides in the dispersed NR phase when the difference value between the interaction parameter of NR/solvent and the interaction parameter of sepiolite nanoclay/solvent is lower than the difference value between the interaction parameter of XNBR/solvent and the interaction parameter of sepiolite nanoclay/solvent.

Impeded repair of abasic site damaged lesions in DNA adsorbed over functionalized multiwalled carbon nanotube and graphene oxide.

The processing of abasic site DNA damage lesions in extracellular DNA in the presence of engineered carbon nanomaterials (CNMs) is demonstrated. The efficacy of the apurinic-apyrimidinic endonuclease 1 (APE1) in the cleavage of abasic site lesions in the presence of carboxylated multi-walled carbon nanotubes (MWCNT-COOH) and graphene oxide (GO) are compared. The CNMs were found to perturb the incision activity of APE1.

Graphene Nanocomposites with High Molecular Weight Poly(ε-caprolactone) Grafts: Controlled Synthesis and Accelerated Crystallization.

Grafting of high molecular weight polymers to graphitic nanoplatelets is a critical step toward the development of high performance graphene nanocomposites. However, designing such a grafting route has remained a major impediment. Herein, we report a "" synthetic pathway by which high molecular weight polymer, poly(ε-caprolactone) (PCL), is tethered, at high grafting density, to highly anisotropic graphitic nanoplatelets.

DNA-melamine hybrid molecules: from self-assembly to nanostructures.

Single-stranded DNA-melamine hybrid molecular building blocks were synthesized using a phosphoramidation cross-coupling reaction with a zero linker approach. The self-assembly of the DNA-organic hybrid molecules was achieved by DNA hybridization. Following self-assembly, two distinct types of nanostructures in the form of linear chains and network arrays were observed.

Synthesis and characterization of a biocompatible monotyrosine-based polymer and its interaction with DNA.

A novel tyrosine-based copolymer containing l-tyrosine (Tyr) and diglycidylether of bisphenol A(DGEBA) was synthesized and studied for its interaction with DNA for potential applications in biological systems. The synthesis of the polymer was optimized by varying monomer ratios using 4-(dimethylamino)pyridine (DMAP) as a catalyst to yield polymers with a M of 7500-8000. Further characterization by FTIR, NMR and thermal analysis supported the formation of the monotyrosine-DGEBA polymer.

Conducting instant adhesives by grafting of silane polymer onto expanded graphite.

A "grafting to" methodology for the attachment of a silane based polymer (SG) onto functionalized graphitic platelets is demonstrated. The siloxy end groups of the modifier were further cross-linked without addition of any external curative. These sterically stabilized nanoplatelets with a high grafting density ensured complete screening of the attractive interparticle interactions.

Processing of abasic site damaged lesions by APE1 enzyme on DNA adsorbed over normal and organomodified clay.

The efficiency of the apurinic/apyrimidinic endonuclease (APE1) DNA repair enzyme in the processing of abasic site DNA damage lesions at precise location in DNA oligomer duplexes that are adsorbed on clay surfaces was evaluated. Three different forms of clay namely montmorillonite, quaternary ammonium salt modified montmorillonite and its boiled counterpart i.e.

Stress generation and tailoring of electronic properties of expanded graphite by click chemistry.

The generation of stress in expanded graphite (E-GPT) due to covalent attachment of bulky side groups connected via a hetero atom is reported. Specifically, E-GPT is modified at different levels of grafting using "click" chemistry to graft 1-ethynyl-4-fluoro benzene onto graphene sheets via a triazole ring. In the range of grafting densitites examined, Raman spectroscopy indicates that the stress generated in graphene is linearly dependent on the extent of grafting.

Polyaniline-carbon nanofiber composite by a chemical grafting approach and its supercapacitor application.

Unlike conventional routes by van der Waals forces, a facile and novel approach using covalent bonding is established in the present work to synthesize polyaniline (PANI)-grafted carbon nanofiber (CNF) composites as promising supercapacitors. For this purpose, toluenediisocyanate was initially functionalized to carboxylated CNF via amidation followed by reaction with excess aniline to form a urea derivative and residual aniline, which was subsequently polymerized and grafted with a urea derivative. Amidation of CNF (TCNF) and, consequently, the grafting of PANI on TCNF were verified by IR, Raman, 1H NMR, X-ray photoelectron, and UV-visible spectroscopic methods, X-ray diffraction, and thermogravimetric analysis.

Bionanowhiskers from jute: preparation and characterization.

Bionanowhiskers were extracted from jute by acid hydrolysis. At first cellulose microfibrils were formed by alkali treatment. Addition of an acid to the microfibrils triggered the formation of cellulose nanowhiskers.

Effect of various nanofillers on thermal stability and degradation kinetics of polymer nanocomposites.

Structure of nanofillers and their subsequent interaction with a polymer is very important in determining thermal stability of polymer nanocomposite. In this paper, we tried to correlate structure of various 0, 1 and 2 dimensional nanofillers with the thermal stability of hydrogenated nitrile butadiene rubber (HNBR) nanocomposites. Organically modified and unmodified layered silicates such as montmorillonite (Cloisite Na+, Cloisite 30B and Cloisite 15A), rod-like fibrous filler (sepiolite) and spherical nanoparticles (nanosilica) were chosen for this purpose.

Nanostructured magnesium oxide as cure activator for polychloroprene rubber.

The aim of this research was to synthesize magnesium oxide nanoparticles and to use them as cure activator for polychloroprene rubber (CR). The effects of counterions of magnesium salts on the homogeneous phase precipitation reaction to control size, monodispersity, crystallinity, and morphology of Mg(OH)2 nanoparticles were also investigated. Magnesium oxide nanoparticles were synthesized by optimizing the calcination temperature of Mg(OH)2 nanoparticles.

Effect of the microstructure of a hyperbranched polymer and nanoclay loading on the morphology and properties of novel polyurethane nanocomposites.

Novel polyurethane nanocomposites based on toluene diisocyanate, poly(propylene glycol), various hyperbranched polymers (HBPs), and layered silicate were synthesized with the aim of determining the effect of the layered silicate loading and the functionality of HBP on the structure and properties of polyurethane nanocomposites. The microstructure of the nanocomposites was investigated by X-ray diffraction analysis and high-resolution transmission electron microscopy. It was found that exfoliated morphology and good dispersion were obtained up to 8 phr clay loading for all of the nanocomposites.

Influence of Nanogels on Mechanical, Dynamic Mechanical, and Thermal Properties of Elastomers.

Use of sulfur crosslinked nanogels to improve various properties of virgin elastomers was investigated for the first time. Natural rubber (NR) and styrene butadiene rubber (SBR) nanogels were prepared by prevulcanization of the respective rubber lattices. These nanogels were characterized by dynamic light scattering, atomic force microscopy (AFM), solvent swelling, mechanical, and dynamic mechanical property measurements.

Influence of Matrix Polarity on the Properties of Ethylene Vinyl Acetate-Carbon Nanofiller Nanocomposites.

A series of ethylene vinyl acetate (EVA) nanocomposites using four kinds of EVA with 40, 50, 60, and 70 wt% vinyl acetate (VA) contents and three different carbon-based nanofillers-expanded graphite (EG), multi-walled carbon nanotube (MWCNT), and carbon nanofiber (CNF) have been prepared via solution blending. The influence of the matrix polarity and the nature of nanofillers on the morphology and properties of EVA nanocomposites have been investigated. It is observed that the sample with lowest vinyl acetate content exhibits highest mechanical properties.

Fabrication and properties of ethylene vinyl acetate-carbon nanofiber nanocomposites.

Carbon nanofiber (CNF) is one of the stiffest materials produced commercially, having excellent mechanical, electrical, and thermal properties. The reinforcement of rubbery matrices by CNFs was studied in the case of ethylene vinyl acetate (EVA). The tensile strength was greatly (61%) increased, even for very low fiber content (i.

Effect of silica nanoparticles on reinforcement of poly(phenylene ether) based thermoplastic elastomer.

Reinforcement of a novel poly(phenylene ether) (PPE) based thermoplastic elastomer (TPE), i.e., styrene-ethylene-butylene-styrene (SEBS)/ethylene vinyl acetate (EVA) and PPE-polystyrene (PS), was studied to develop a reinforced thermoplastic elastomer or thermoplastic vulcanizate (TPV).

Influence of functionalization of multi-walled carbon nanotubes on the properties of ethylene vinyl acetate nanocomposites.

Commercially available multiwalled carbon nanotubes (MWNT) were chemically modified by amine, acid and silane and their ethylene vinyl acetate (EVA) based nanocomposites were prepared. Unmodified and modified nanotubes were characterized by thermogravimetry, X-ray diffraction, Raman spectroscopy, X-ray photoelectron spectroscopy and transmission electron microscopy. Early degradation of modified nanotubes from the thermogravimetry study proved the presence of functional groups on nanotube surface.

Comparative studies on crosslinked and uncrosslinked natural rubber biodegradation by Pseudomonas sp.

A comparative study on biodegradation of di-cumyl peroxide (DCP) crosslinked and uncrosslinked natural rubber by Pseudomonas sp. was carried out. Decrease in organic carbon content along with the changes in tensile strength of the treated rubber, both DCP crosslinked and uncrosslinked natural rubber, indicated rubber hydrocarbon utilization by the Pseudomonas sp.