6 research outputs found

    Graphene ink laminate structures on poly(vinylidene difluoride) (PVDF) for pyroelectric thermal energy harvesting and waste heat recovery

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    Thermal energy can be effectively converted into electricity using pyroelectrics, which act as small scale power generator and energy harvesters providing nanowatts to milliwatts of electrical power. In this paper, a novel pyroelectric harvester based on free-standing poly­(vinylidene difluoride) (PVDF) was manufactured that exploits the high thermal radiation absorbance of a screen printed graphene ink electrode structure to facilitate the conversion of the available thermal radiation energy into electrical energy. The use of interconnected graphene nanoplatelets (GNPs) as an electrode enable high thermal radiation absorbance and high electrical conductivity along with the ease of deposition using a screen print technique. For the asymmetric structure, the pyroelectric open-circuit voltage and closed-circuit current were measured, and the harvested electrical energy was stored in an external capacitor. For the graphene ink/PVDF/aluminum system the closed circuit pyroelectric current improves by 7.5 times, the open circuit voltage by 3.4 times, and the harvested energy by 25 times compared to a standard aluminum/PVDF/aluminum system electrode design, with a peak energy density of 1.13 μJ/cm<sup>3</sup>. For the pyroelectric device employed in this work, a complete manufacturing process and device characterization of these structures are reported along with the thermal conductivity of the graphene ink. The material combination presented here provides a new approach for delivering smart materials and structures, wireless technologies, and Internet of Things (IoT) devices

    Solvothermal nanoYAG synthesis: mechanism and particle growth kinetics

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    NanoYAG particles with spherical morphology have been synthesised using a solvothermal method; a structure sensitive reaction, where the chemical reaction and the particle growth kinetics are interdependent. It has been observed that the primary YAG particles agglomerated into ∼30 nm clusters via a self-assembled Ostwald ripening process along (2 1 1) planes, separated by a distance of ∼0.49 nm, at 270 °C and 2.0 MPa for 2 h. These nanoclusters coalesced into single nanoparticles of ∼30 nm in size and exhibited a smaller inter planar distance of ∼0.26 nm, corresponding to the (4 2 0) planes, when synthesized at 300 °C and 8.5 MPa for 2 h. in addition, the solvent 1,4-butanediol transformed into 1,4-diacetoxybutane, this will have undergone esterification by reacting with the terminal acetate groups cleaved from the precursor, yttrium acetate. The proposed mechanism based on the analytical evidence suggests that a complete dissolution of precursors facilitated the structural re-arrangement of atoms within the planes and lead to a significantly higher degree of crystallinity. Moreover, once the particles with (4 2 0) planes had formed, they were no longer involved in facile coalescence along their preferential planes due to their lower interfacial energy compared to the (2 1 1) planes. This led to control of the particle morphology and with little agglomeration occurring in the final nanopowder

    Improving the fracture toughness properties of epoxy using graphene nanoplatelets at low filler content

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    This paper reports improvement in the fracture properties of epoxy nanocomposites using plasma functionalized graphene nanoplatelets (f-GNP) at low filler content. Various mechanical tests were performed on a series of f-GNP/epoxy at low nanofiller loading to assess the effect of the nanofiller on mechanical properties. Most importantly, a significant enhancement in fracture toughness is achieved without compromising the tensile and thermal properties of the nanocomposites. The fracture toughness of neat epoxy resin was increased by over 50% with the incorporation of 0.25 wt% f-GNP loading, obtaining a value of 245 J m−2, while the neat epoxy indicated a value of 162 J m−2. The glass transition temperature (Tg) and coefficient of thermal expansion (CTE) both showed a slight increase of 3% and 2%, respectively, both at 1 wt% f-GNP loading. These enhancements are competitive with current literature results on nanocomposites, but at significantly lower filler content. We therefore demonstrate that f-GNPs are capable of providing effective toughening of epoxy resins, while maintaining other tensile and thermal properties

    A comparative study of the synthesis of nanocrystalline Yttrium Aluminium Garnet using sol-gel and co-precipitation methods

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    This paper is in closed access.Nanocrystalline yttrium aluminium garnet (nYAG) powder has been synthesized via sol-gel and co-precipitation methods using nitrate precursors. Thermal evolution and crystallisation kinetics of both the methods were investigated. The optimised calcination condition for the formation of nYAG was also examined. It was found that a complete transformation to nYAG was observed at 925 C/2 h and 1000 C/1 h for the coprecipitation and sol-gel samples respectively. An intermediate YAlO3 phase was formed at 900 C in all powders regardless of the synthesis methods. The powder morphologies obtained from TEM revealed very similar particle sizes for the two routes (20-30 nm); whilst the extent of agglomeration was higher for the sol-gel method. It was also observed that by controlling the pH in a narrow range, maintaining the precipitate processing temperature and dehydrating excess OH- ions in the precipitates using n-butanol treatment, the extent of agglomeration was further reduced in the co-precipitated nYAG powder. © 2013 Elsevier Ltd and Techna Group S.r.l

    Application of Ozone-Assisted Membrane Cleaning for Natural Organic Matter Fouled Membranes

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    The popularity of membrane technology in water treatment has been rising for over last 50 years due to wide range of filtration processes and applications, cost effective production and installation as well as safe and efficient water production. However, the development and improvement of membranes is ongoing due to number of weaknesses. Membrane fouling is a major drawback of membrane application in water and waste water treatment. Mostly caused by natural organic matter (NOM), fouling forms a layer on top of the membrane and blocks pores reducing the water permeation and can be potentially destructive to the membrane structure. The issue of membrane fouling can be addressed during membrane manufacturing, maintenance and operation. In the current study, the graphene-based nanomaterials (GBN) were incorporated in polyvinylidene fluoride (PVDF) to manufacture membranes via the phase-inversion technique. The resulting membranes show significant improvement to the properties of the pure PVDF membranes and their antifouling ability. The addition of GBN enhanced the water permeation by over 79% as a result of increased membrane hydrophilicity. Although this enhancement is beneficial, membrane fouling remained an issue despite the observed improvement. In this study, ozone, which is an effective oxidant, was evaluated as a novel technique for the cleaning of humic acid-fouled membranes. When ozone cleaning was applied to the humic acid-fouled membranes, reestablishment of close to original flux values was observed after just 30 min of cleaning. This statement is supported by SEM images that give an insight into the fouling of the membrane surface after the application of the cleaning methods. The data indicate that ozone is an effective technique for membrane cleaning against NOM-induced fouling

    A comparative study of the synthesis of nanocrystalline Yttrium Aluminium Garnet using sol-gel and co-precipitation methods

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    Nanocrystalline yttrium aluminium garnet (nYAG) powder has been synthesized via sol-gel and co-precipitation methods using nitrate precursors. Thermal evolution and crystallisation kinetics of both the methods were investigated. The optimised calcination condition for the formation of nYAG was also examined. It was found that a complete transformation to nYAG was observed at 925 C/2 h and 1000 C/1 h for the coprecipitation and sol-gel samples respectively. An intermediate YAlO3 phase was formed at 900 C in all powders regardless of the synthesis methods. The powder morphologies obtained from TEM revealed very similar particle sizes for the two routes (20-30 nm); whilst the extent of agglomeration was higher for the sol-gel method. It was also observed that by controlling the pH in a narrow range, maintaining the precipitate processing temperature and dehydrating excess OH- ions in the precipitates using n-butanol treatment, the extent of agglomeration was further reduced in the co-precipitated nYAG powder. © 2013 Elsevier Ltd and Techna Group S.r.l
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