Active food packaging films from Carboxy methyl cellulose and starch (CMC-g-Starch) reinforced with Magnesium-oxide (MgO) NPs are created and characterized. The effect of different particle sizes, MgO NPs concentrations and different gamma irradiation doses on the preparation of (CMC-g-Starch-MgO) edible nanocomposite films were investigated to determine their properties. Several analytical methods, such as swelling behavior, FT-IR, TEM, TGA, and mechanical characteristics, are represented to investigate different characteristics of the prepared (CMC-g-Starch-MgO) edible nanocomposite films. Also, the prepared (CMC-g-Starch-MgO) edible nanocomposite films and their coating were subjected to the fresh Peaches fruits. Their effect on the Peach fruits' lifespan was evaluated. The anti-microbial property of the edible (CMC-g-Starch-MgO) nanocomposite films of gram (+ve) and gram (–ve) bacteria was reported. Results represented the thermal and mechanical characteristics of (CMC-g-Starch-MgO) edible nanocomposite films, which were enhanced by γ irradiation. Also, the irradiated (CMC-g-Starch-MgO) edible nanocomposite films and their coating extend the lifespan of Peaches fruits and exhibit resistance to pathogenic microorganisms. In conclusion, (CMC-g-Starch-MgO) edible nanocomposite films fulfilled the required behaviors for the application in the nanofood packaging era.

A study on electrical conduction of carbon/epoxy laminates has so far been conducted in an ad hoc nature without a standardised method, involving many extrinsic factors. How these factors affect electrical conduction of carbon/epoxy laminates has not been well established. The objectives of this work are to ascertain the effects of electrical currents, temperatures, and clamping torques on the anisotropic electrical conduction of carbon/epoxy laminates. Two-probe method with solid electrodes was developed with machined carbon/epoxy laminate specimens of various dimensions. The contributions of elevated temperatures and clamping pressures to electrical conduction were investigated. Various contact conditions with or without conductive paint were examined. The relationship of electrical resistance correlating with temperature and clamping pressure was developed to aid an analysis of data trends. From the average test results of 18 groups, aided with qualitative predictions, the milliampere-to-ampere increases of current led to significant reductions in electrical conductivities in both in-plane and through-the-thickness directions. The rises of temperatures resulted in the similar reductions in electrical conductivity due to the increased resistance. The increase in clamping torque increased the electrical conductivity values in both directions. Applying conductive paint to the contact faces did not appear to affect the contact resistance. Thus, the enhanced values of electrical conductivity from the painted specimens were attributed to their lower body temperatures, as the conductive paint at the contact faces soaked up the substantial amount of the electrical energies.

Lack of access to potable water and abating levels of ground water level demands the reuse of unconventional water sources after remediating it in a sustainable way. In this context, purifying brackish, land and sea water seems a feasible solution to the ever-growing population.In this work, a novel composite membrane was fabricated by 'layer-by-layer' self-assembly of poly-dopamine (PDA) and polystyrene sulfonate (PSS) supported on a highly crosslinked graphene oxide (GO) membrane to sieve ions to purify contaminated water as well as enhance the resistance towards chlorine. This GO membrane was sandwiched between layers of various nanoporous polyvinylidene difluoride (PVDF) membranes obtained by selectively etching out the PMMA component from the demixed blends. The blend membranes were designed following the melt-extrusion process and subsequent quenching to facilitate confined crystallization of PVDF and selective etching of PMMA. The membranes with different pore sizes were tuned on varying the composition in blends and a gradient in microstructure was achieved by stitching the membranes. Pure water flux, salt rejection, dye removal, and antibacterial activity were performed to study the membrane's efficiency. The GO membrane was chemically crosslinked with methylenediamine to impart dimensional stability and to enhance rejection efficiency through the nanoslits that GO offers. Besides effective rejection, the sandwiched membrane was modified with ‘layer-by-layer’ self-assembly of polyelectrolytes on the surface to improve the chlorine tolerance performance. This strategy resulted in an excellent salt (about 95% and 97% for monovalent and divalent ion, respectively) and dye rejection (100% for both cationic and anionic dye), besides facilitating excellent chlorine tolerance performance. Moreover, this modified membrane showed superior antifouling properties (flux recovery ratio is more than 90%) and excellent antibacterial performance (near about 3 log reduction).Thus the concept of using layer-by-layer self-assembly of polycations (PDA) and polyanions (PSS) onto a hierarchical chemically modified GO sandwiched PVDF membrane proved to be a productive strategy to purify contaminated water. Thus the membrane can be a potential candidate for domestic as well as industrial application.

The interface between polymer matrices and nanofillers is critical for efficient interaction to achieve the desired final properties. In this work, block copolymers were utilized to control the interface and achieve optimum interfacial interaction. Specifically, we studied the compatibilizing effects of styrene-ethylene/butadiene-styrene (SEBS) and styrene-ethylene/propylene (SEP) block copolymers on the morphology, conductivity, and rheological properties of polypropylene-polystyrene (PP/PS) immiscible blend with 2 vol% multiwall carbon nanotube (MWCNT) at different blend compositions of PP/PS 80:20, 50:50 and 20:80.MWCNTs induced co-continuity in PP/PS blends and did not obstruct with the copolymer migration to the interface. Copolymers at the interface led to blend morphology refinement. Adding block copolymers at a relatively low concentration of 1 vol% to compatibilize the PP/PS 80:20 blend substantially increased the electrical conductivity from 5.15*10−7S/cm for the uncompatibilized blend to 1.07*10−2S/cm for the system with SEP and 1.51*10−3S/m for the SEBS system. These values for the compatibilized blends are about 4 orders of magnitude higher due to the interconnection of the droplet domains. For the PP/PS 50:50 blend, the SEBS copolymer resulted in a huge increase in conductivity at above 3 vol% concentration (conductivity increased to 3.49*10−3S/cm from 5.16*10−7S/cm). Both the conductivity and the storage modulus increased as the SEBS copolymer content was increased. For the PP/PS 20:80 blend, we observed an initial decrease in conductivity at lower copolymer concentrations (1–3 vol%) and then an increase in conductivity to values higher than the uncompatibilized system, but only at a higher copolymer concentration of 10 vol%. The triblock copolymer (SEBS), which had 60 wt% PS content, shows a more significant increase in rheological properties compared to the diblock copolymer (SEP). The morphology shows that the interaction between MWCNT and PS is stronger than the interaction between MWCNT and PP, hence there is selective localization of the nanofiller in the PS phase as predicted by Young’s equation and by molecular simulation.

Conventional carbon fibre laminates are known to be moderately electrically conductive in-plane, but have a poor through-thickness conductivity. This poses a problem for functionality aspects that are of increasing importance to industry, such as sensing, current collection, inductive/resistive heating, electromagnetic interference (EMI) shielding, etc. This restriction is of course more pronounced for non-conductive composite reinforcements such as glass, organic or natural fibres. Among various solutions to boost through-thickness electrical conductivity, tufting with hybrid micro-braided metal-carbon fibre yarns is one of the most promising. As a well-characterised method of through thickness reinforcement, tufting is easily implementable in a manufacturing environment. The hybridisation of materials in the braid promotes the resilience and integrity of yarns, while integrating metal wires opens up a wide range of multifunctional applications. Many configurations can be produced by varying braid patterns and the constituting yarns/wires. A predictive design tool is therefore necessary to select the right material configuration for the desired functional and structural performance. This paper suggests a fast and robust method for generating finite-element models of the braids, validates the prediction of micro-architecture and electrical conductivity, and demonstrates successful manufacturing of composites enhanced with braided tufts.

The aim of this study was to identify the effect of material type (matrix and reinforcement) and process parameters, on the mechanical properties of 3D Printed long-fibre reinforced polymer composites manufactured using a commercial 3D Printer (Mark Two). The effect of matrix material (Onyx or polyamide), reinforcement type (Carbon, Kevlar®, and HSHT glass), volume of reinforcement, and reinforcement lay-up orientation on both Ultimate Tensile Strength (UTS) and Flexural Modulus were investigated.For Onyx, carbon fibre reinforcement offered the largest increase in both UTS and Flexural Modulus over unreinforced material (1228 ± 19% and 1114 ± 6% respectively). Kevlar® and HSHT also provided improvements but these were less significant. Similarly, for Nylon, the UTS and Flexural Modulus were increased by 1431 ± 56% and 1924 ± 5% by the addition of carbon fibre reinforcement. Statistical analysis indicated that changing the number of layers of reinforcement had the largest impact on both UTS and Flexural Strength, and all parameters were statistically significant.