Studies on the physico‐mechanical,thermal, and morphological behaviors of high density polyethylene/coleus spent green composites

This study is aimed at utilizing nutraceutical industrial waste and reducing carbon footprints of plastics. Eco‐friendly “green composites” of high density polyethylene (HDPE) were fabricated using coleus spent (CS)—a nutraceutical industrial waste as reinforcing filler and maleic anhydride‐graft‐polyethylene (MA‐g‐PE) as compatibilizer. Composites were fabricated with 5, 10, 15, and 20% (w/w) of CS by extrusion method. The fabricated HDPE/CS composites were evaluated for mechanical and thermal behavior. A slight improvement of about 5% in tensile strength and marked improvement of about 25% in tensile modulus for 20 wt % CS filled HDPE composites was noticed. The effect of CS content on rheological behavior was also studied. Thermal characteristics were performed using thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC). TGA thermogram indicated increased thermal stability of CS‐filled composites. From TGA curves the thermal degradation kinetic parameters of the composites have been calculated using Broido's method. The enthalpy of melting (ΔH_m) obtained from DSC curves was reduced with increase in CS content in HDPE matrix, due to decrease in HDPE content in composite systems. An increase in CS loading increased the water absorption behavior of the composites slightly. Morphological behavior of cryo‐fractured composites has been studied using scanning electron microscopy. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Influence of plasticizers (DOP and CNSL) on mechanical and electrical properties of SBS/polyaniline blends

Electrically conductive blends based on polyaniline-dodecylbenzene sulfonic acid (Pani.DBSA)/styrene-butadiene-styrene (SBS) block copolymer have been prepared in the presence of different plasticizers such as dioctyl phthalate (DOP) and cashew nut shell liquid (CNSL). The products were characterized by ultraviolet-visible (UV-vis) spectrometry, scanning electron microscopy, X-ray diffraction, electron paramagnetic resonance (EPR) and resistivity measurements. The presence of DOP resulted in an increase of the electrical resistivity whereas the increasing concentration of CNSL resulted in a decrease of electrical resistivity. In the latter case, the presence of cardanol, a phenol-type compound in CNSL, may be responsible for the improved electrical performance, probably because of a secondary doping process, which changes the molecular conformation of Pani.DBSA chains from “compact coil” to “expanded coil”. In addition, CNSL contributes to the formation of cocontinuous-type morphology with conducting pathways in larger extension. EPR studies also showed an increase of the polaron mobility as the amount of CNSL in the blend increases.     

Influence of free volume on the mechanical properties of Epoxy/poly (methylmethacrylate) blends

Positron lifetime measurements have been performed to investigate the free volume dependence of the mechanical properties of Epoxy/poly methyl methacrylate (PMMA) blends of varying composition of PMMA (2.5, 5, 7.5, 10, 12.5, 15, and 17.5 wt%). The mechanical properties of the blends have been evaluated according to the (ASTM) standard. The positron results indicate that the mechanical properties like tensile strength and surface hardness have a significant dependence on the free volume of the blends. It is also found that the blends of the present study show positive deviation from the familiar linear additivity rule suggesting the immiscible nature of the blends. Further, up to 5-wt% of PMMA in the blend, an increase in relative fractional free volume correlates well with a decrease of tensile strength.     

Investigation on miscibility behaviors of elastin‐like polypentapeptide blends with polyvinyl alcohol in aqueous and solid state

The polypentapeptide of elastin, poly(GVGVP) has shown remarkable properties and have great potential for biomedical applications. To explore its applications further, the miscibility behaviors of poly(vinyl alcohol) (PVA)/poly(GVGVP) blends have been explored in a very broad composition range. The miscibility behaviors of these blends have been investigated in both solution and solid state using various analytical techniques, including ultrasonic velocity, density, refractive index (RI) and viscosity techniques at 25 °C. The results confirmed the miscibility of the blend up to 40% of the polypeptide. This was further supported by Fourier transform infrared (FTIR) spectroscopy, differential scanning calorimetry (DSC) and scanning electron microscopy (SEM). © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 44624.     

Structure–property relationship of starch‐filled chain‐extended polyurethanes

Chain‐extended polyurethane (PU) elastomers were prepared using castor oil with 4,4′‐methylene bis (phenyl isocyanate) (MDI) as a crosslinker and 4,4′‐diamino diphenyl sulphone (DDS) as an aromatic diamine chain extender. A series of starch‐filled (from 5 to 25% wt/wt) diamines chain‐extended PUs have been prepared. The starch‐filled PU composites were characterized for physico‐mechanical properties viz, density, surface hardness, tensile strength, and percentage elongation at break. Thermal stability of PU/starch have been carried out by using thermogravimetric analyzer (TGA). Thermal degradation process of PU/starch were found to proceed in three steps. TGA thermograms of PU/starch shows that all systems were stable upto 235°C, and maximum weight loss occur at temperature 558°C. The microcrystalline parameters such as crystal size (〈N〉) and lattice strain (g in %) of PU/starch have been established using wide‐angle X‐ray scattering (WAXS) method. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 90: 2945–2954, 2003     

Investigation of multi‐walled carbon nanotube‐reinforced high‐density polyethylene/carbon black nanocomposites using electrical,DSC and positron lifetime spectroscopy techniques

BACKGROUND: The positive temperature coefficient (PTC) effect on material properties has attracted much attention in recent years due to the prospects of many applications like temperature sensors, thermistors, self‐regulating heaters, etc. It has been suggested that incorporation of multi‐walled carbon nanotubes (MWNTs) into carbon black (CB)‐filled polymers could improve the electrical properties of composites due to high conductivity and network structure and significantly reduce the required CB loading. RESULTS: We observed no change in melting temperature and crystalline transition temperature on addition of MWNTs. However, the heat of fusion decreases as the amount of conducting carboxylated MWNT (c‐MWNT) filler increases and the resistivity of the composite decreases. The free volume shows an increase up to 1.5 wt% of c‐MWNT content and then decreases. CONCLUSION: Well‐developed crystals could not be formed due to restricted chain mobility as filler content increases. This results in minimum intermolecular interactions, and thus a decreased heat of fusion. A composite with c‐MWNT content of 0.5 wt% showed the highest PTC and higher resistivity at 150 °C possibly due to the formation of flocculated structures at elevated temperature. For filler content greater than 1.5 wt%, the decrease in free volume may be due to restricted chain mobility. Copyright © 2009 Society of Chemical Industry     

The influence of zinc oxide–cerium oxide nanoparticles on the structural characteristics and electrical properties of polyvinyl alcohol films

With the objective to investigate the influence of zinc oxide–cerium oxide (ZnO–Ce₂O₃) nanoparticles on the electrical properties of polyvinyl alcohol (PVA), PVA/ZnO–Ce₂O₃ nanocomposite films were prepared by solution intercalation method with different weight percentage viz., 0.5, 1.0, and 2.0?wt% of ZnO–Ce₂O₃ nanoparticles. The fabricated nanocomposites were characterized by Fourier transform-infrared spectroscopy (FT-IR), X-ray diffraction (XRD), and differential scanning calorimetry (DSC). The effect of ZnO–Ce₂O₃ nanoparticles on the dielectric constant (ε′), dielectric loss (ε″), electric modulus (M′ and M″), ac conductivity (σ _ac), and dielectric loss tangent (tan δ) over a range of frequencies at room temperature of PVA nanocomposites have been studied. FT-IR, XRD, and DSC analysis indicates the nature of ZnO–Ce₂O₃ nanoparticles interaction with the PVA matrix. The morphological behavior of the nanocomposites has been performed using scanning electron microscopy (SEM). The dielectric behaviors such as dielectric constant (ε′) and dielectric loss (ε″) increases with increase in nanoparticle concentration, but decreases with increase in frequency. But, the electric modulus (M′) increases with increase in frequency. Dielectric loss tangent (tan δ) decreases with increase in filler content at lower frequency, but at higher frequencies the tan δ increases with increase in nanoparticles content. AC conductivity (σ _ac) of PVA/ZnO–Ce₂O₃ nanocomposites increases with increasing frequency following the universal dielectric response law.     

Ethylene Methacrylate (EMA) Co-polymer Toughened Polymethyl Methacrylate Blends: Physico-mechanical,Optical, Thermal and Chemical Properties

Polymethyl methacrylate (PMMA) was blended with ethylene methacrylate (EMA) copolymer in different compositions by melt mixing technique using Haake Rheochord twin screw extruder. The physico-mechanical, thermal, optical and chemical properties of PMMA/EMA blends were investigated with special reference to the blend compositions. The impact strength of the blends was found to increase significantly with increase in EMA content, without affecting the optical properties significantly. Optical micrograph images of the blends reveals that the rubbery phase dispersed as domains in the continuous PMMA matrix at 5 and 10 wt. % addition of EMA. The PMMA/EMA, 80/20 blend was found to exist as co-continuous system. Attempts have been made to correlate changes in morphology with mechanical properties. The influence of chemical ageing and heat ageing on the mechanical performance of PMMA/EMA blends has been studied. Four composite models such as series model, parallel model, Hapin-Tsai and Kerner's model have been used to fit the experimental tensile strength, tensile modulus and surface hardness.     

Microstructure,thermal, physico–mechanical and tribological characteristics of molybdenum disulphide‐filled polyamide 66/carbon black composites

With an objective to investigate the influence of molybdenum disulphide (MoS₂) on physico–mechanical and tribological properties of polyamide 66 (PA 66), was compounded with MoS₂ in the presence of carbon black (CB). The compounded material was injection molded to make test specimens to evaluate physico–mechanical, thermal, and tribological (wear, friction, and laser etching) characteristics. It was found that tensile strength, percentage elongation at break, and tensile modulus of PA 66/CB/MoS₂ composite increased linearly with increase in MoS₂ content. The impact strength of the PA 66 matrix increased from 37.2 to 43.2 J/m with an increase in MoS₂ content. The wear behavior of PA 66/CB/MoS₂ composites have been investigated under dry sliding conditions at different normal loads, sliding distances, and sliding velocities at room temperature. It was found that the introduction of MoS₂ in the presence of CB has certainly reduced the friction, wear behavior of PA 66 with improvement in laser etching resistance. MoS₂ could increase the adhesion between the transfer film and the counterface surface. The ability of the synergistic fillers in helping the formation of thin, uniform, and continuous transfer film would contribute to enhance the wear resistance of PA 66 composites. POLYM. ENG. SCI., 2013. © 2012 Society of Plastics Engineers     

Molecular transport of n‐alkanes through diol chain‐extended polyurethane membranes

Molecular transport of n‐alkanes was investigated by calculating sorption, diffusion, and permeation of liquids through the diol chain‐extended polyurethane (PU) membranes in the temperature interval 25–60°C. Sorption experiments were performed gravimetrically. Diffusion coefficients were calculated from Fick's equation. These results showed a dependency on the nature and size of interacting n‐alkane molecules as well as morphology of the chain‐extended PUs. Transport kinetics followed an anomalous trend. Using the temperature‐dependent transport parameters, activation energies were calculated for diffusion and permeation processes using an Arrhenius equation. The van't Hoff relationship was used to obtain enthalpy and entropy of sorption. Concentration profiles of liquids through PU membranes were computed using Fick's equation, solved under appropriate initial and boundary conditions. A correlation was attempted between transport properties of liquids and physicomechanical properties of PU membranes. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 96: 874–882, 2005