9 results on '"Huson, Mickey G"'
Search Results
2. Heterogeneity of carbon fibre.
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Huson, Mickey G., Church, Jeffrey S., Kafi, Abdullah A., Woodhead, Andrea L., Khoo, Jiyi, Kiran, M.S.R.N., Bradby, Jodie E., and Fox, Bronwyn L.
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PAN-based carbon fibers , *STIFFNESS (Mechanics) , *INTERMEDIATES (Chemistry) , *RAMAN spectroscopy , *SURFACE energy , *GAS chromatography - Abstract
Abstract: A range of polyacrylonitrile (PAN) and pitch based carbon fibre types (high, standard and intermediate modulus fibres) have been characterised using both physical and chemical techniques, the results highlighting the heterogeneity of the fibre. Nano-indentation showed variation in stiffness between different fibres of the same type as well as variation along a 20μm length of a single fibre. Tensile tests showed variance of approximately 25% in tenacity for three different carbon fibre types but less variability in modulus with values from 8% to 19%. Raman spectroscopy showed variation in the graphitic content both between fibres of different origin as well as variation, with 0.5μm spatial resolution, along the length of a single fibre. Inverse gas chromatography surface energy measurements of larger samples of fibres were carried out using the novel approach of incremental surface coverage by varying the probe molecule concentration and revealed different levels of energetic heterogeneity for PAN based fibres collected at different stages of carbon fibre production. The heterogeneity of the unoxidised fibres (collected after carbonisation) was restricted to about 15% of the fibre surface whereas the surface oxidised fibre sample (collected after the electrolytic oxidation bath) was heterogeneous over more than 30% and the sized fibres were shown to be quite homogeneous. [Copyright &y& Elsevier]
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- 2014
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3. The development of photochemically crosslinked native fibrinogen as a rapidly formed and mechanically strong surgical tissue sealant
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Elvin, Christopher M., Brownlee, Alan G., Huson, Mickey G., Tebb, Tracy A., Kim, Misook, Lyons, Russell E., Vuocolo, Tony, Liyou, Nancy E., Hughes, Timothy C., Ramshaw, John A.M., and Werkmeister, Jerome A.
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FIBRINOGEN , *BIOMEDICAL materials , *HYDROGELS , *TYROSINE , *MOLECULE-molecule collisions , *CHEMICAL bonds - Abstract
Abstract: We recently reported the generation of a highly elastic, crosslinked protein biomaterial via a rapid photochemical process using visible light illumination. In light of these findings, we predicted that other unmodified, tyrosine-rich, self-associating proteins might also be susceptible to this covalent crosslinking method. Here we show that unmodified native fibrinogen can also be photochemically crosslinked into an elastic hydrogel biomaterial through the rapid formation of intermolecular dityrosine. Photochemically crosslinked fibrinogen forms tissue sealant bonds at least 5-fold stronger than commercial fibrin glue and is capable of producing maximum bond strength within 20s. In vitro studies showed that components of the photochemical crosslinking reaction are non-toxic to cells. This material will find useful application in various surgical procedures where rapid curing for high strength tissue sealing is required. [Copyright &y& Elsevier]
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- 2009
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4. Carbon fibre surface modification using functionalized nanoclay: A hierarchical interphase for fibre-reinforced polymer composites.
- Author
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Zabihi, Omid, Ahmadi, Mojtaba, Li, Quanxiang, Shafei, Sajjad, Huson, Mickey G., and Naebe, Minoo
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CLAY-reinforced polymeric nanocomposites , *CARBON fibers , *SURFACE roughness , *WEIBULL distribution , *INVERSE gas chromatography - Abstract
Low interface strength is a common challenge in taking full advantage of excellent physical performances of carbon fibre (CF) reinforced polymer composites. Herein, for the first time, we have used amino-functionalized nanoclay as a linkage between CF surface and epoxy matrix, which by a cation exchange process was grafted on the CF surface. Amino-functionalized nanoclay significantly increased surface roughness, coefficient of friction, and BET surface area of CF. The results showed that nanoclay-based modification does not change the tensile strength and Weibull modulus of CF significantly however, both specific and dispersive surface energies, obtained by inverse gas chromatography technique, were increased. A high compatibility of nanoclay-based modified CF (clay@CF) with epoxy resin was also observed by analysing the contact angle between epoxy droplets and fibre surface. Moreover, single fibre fragmentation tests (SFFT) alongside fractographic observations showed that the length of fibre pull-out and the size of cracks between the fibre and matrix were outstandingly reduced in clay@CF in comparison to untreated CF, demonstrating that the stress transfer and interfacial shear strength (IFSS) have been significantly improved. [ABSTRACT FROM AUTHOR]
- Published
- 2017
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5. A systematic study of carbon fibre surface grafting via in situ diazonium generation for improved interfacial shear strength in epoxy matrix composites.
- Author
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Beggs, Kathleen M., Servinis, Linden, Gengenbach, Thomas R., Huson, Mickey G., Fox, Bronwyn L., and Henderson, Luke C.
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CARBON , *EPOXY compounds , *COMPOSITE materials , *SURFACE grafting (Polymer chemistry) , *DIAZONIUM compounds , *SHEAR strength - Abstract
A recently established means of surface functionalization of unsized carbon fibres for enhanced compatibility with epoxy resins was optimised and evaluated using interfacial shear stress measurements. Interfacial adhesion has a strong influence on the bulk mechanical properties of composite materials. In this work we report on the optimisation of our aryl diazo-grafting methodology via a series of reagent concentration studies. The fibres functionalised at each concentration are characterised physically (tensile strength, modulus, coefficient of friction, and via AFM), and chemically (XPS). The interfacial shear strength (IFSS) of all treated fibres was determined via the single fibre fragmentation test, using the Kelly–Tyson model. Large increases in IFSS for all concentrations (28–47%) relative to control fibres were observed. We show that halving the reagent concentration increased the coefficient of friction of the fibre and the interfacial shear strength of the composite while resulting in no loss of the key performance characteristics in the treated fibre. [ABSTRACT FROM AUTHOR]
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- 2015
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6. Surface functionalization of unsized carbon fiber using nitrenes derived from organic azides
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Servinis, Linden, Henderson, Luke C., Gengenbach, Thomas R., Kafi, Abdullah A., Huson, Mickey G., and Fox, Bronwyn L.
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CARBON fibers , *SURFACE chemistry , *NITRENES , *AZIDES , *AZIRIDINES , *REACTIVITY (Chemistry) - Abstract
Abstract: The surface of both oxidized and unoxidized unsized carbon fiber was functionalized using an aziridine linking group derived from reactive nitrenes. The aziridine functionality arose from the cyclization of a reactive nitrene species onto the highly electron rich graphitic surface of the carbon fibers; the nitrene species evolved from thermal N2 elimination from the corresponding (room temperature stable) azide. Surface functionalization using the nitrene approach was supported by X-ray Photoelectron Spectroscopy, in both oxidized and unoxidized carbon fiber. Attempts were also made to functionalize using amide chemistry, the two-step acid chloride coupling being successful for oxidized fibers by utilizing the carboxylic acid rich defect sites on the carbon fiber. None of the chemical treatment pathways had a significant impact on the tensile strength of the individual fibers, and atomic force microscopy revealed that fibers undergoing these treatment methodologies remained intact, without creating additional surface defects. [Copyright &y& Elsevier]
- Published
- 2013
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7. Molecular and functional characterisation of resilin across three insect orders
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Lyons, Russell E., Wong, Darren C.C., Kim, Misook, Lekieffre, Nicolas, Huson, Mickey G., Vuocolo, Tony, Merritt, David J., Nairn, Kate M., Dudek, Daniel M., Colgrave, Michelle L., and Elvin, Christopher M.
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RESILIN , *ELASTOMERS , *BIOMEDICAL materials , *MICROSCOPY , *GENETIC transcription , *RNA , *AMINO acid sequence , *ESCHERICHIA coli - Abstract
Abstract: Resilin is an important elastomeric protein of insects, with roles in the storage and release of energy during a variety of different functional categories including flight and jumping. To date, resilin genes and protein function have been characterised only in a small number of flying insects, despite their importance in fleas and other jumping insects. Microscopy and immunostaining studies of resilin in flea demonstrate the presence of resilin pads in the pleural arch at the top of the hind legs, a region responsible for the flea’s jumping ability. A degenerate primer approach was used to amplify resilin gene transcripts from total RNA isolated from flea (Ctenocephalides felis), buffalo fly (Haematobia irritans exigua) and dragonfly (Aeshna sp.) pharate adults, and full-length transcripts were successfully isolated. Two isoforms (A and B) were amplified from each of flea and buffalo fly, and isoform B only in dragonfly. Flea and buffalo fly isoform B transcripts were expressed in an Escherichia coli expression system, yielding soluble recombinant proteins Cf-resB and Hi-resB respectively. Protein structure and mechanical properties of each protein before and after crosslinking were assessed. This study shows that resilin gene and protein sequences are broadly conserved and that crosslinked recombinant resilin proteins share similar mechanical properties from flying to jumping insects. A combined use of degenerate primers and polyclonal sera will likely facilitate characterisation of resilin genes from other insect and invertebrate orders. [Copyright &y& Elsevier]
- Published
- 2011
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8. A highly elastic tissue sealant based on photopolymerised gelatin
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Elvin, Christopher M., Vuocolo, Tony, Brownlee, Alan G., Sando, Lillian, Huson, Mickey G., Liyou, Nancy E., Stockwell, Peter R., Lyons, Russell E., Kim, Misook, Edwards, Glenn A., Johnson, Graham, McFarland, Gail A., Ramshaw, John A.M., and Werkmeister, Jerome A.
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ELASTIC tissue , *SEALING compounds , *PHOTOPOLYMERIZATION , *GELATIN , *CROSSLINKING (Polymerization) , *BIOMEDICAL materials - Abstract
Abstract: Gelatin is widely used as a medical biomaterial because it is readily available, cheap, biodegradable and demonstrates favourable biocompatibility. Many applications require stabilisation of the biomaterial by chemical crosslinking, and this often involves derivatisation of the protein or treatment with cytotoxic crosslinking agents. We have previously shown that a facile photochemical method, using blue light, a ruthenium catalyst and a persulphate oxidant, produces covalent di-tyrosine crosslinks in resilin and fibrinogen to form stable hydrogel biomaterials. Here we show that various gelatins can also be rapidly crosslinked to form highly elastic (extension to break >650%) and adhesive (stress at break >100kPa) biomaterials. Although the method does not require derivatisation of the protein, we show that when the phenolic (tyrosine-like) content of gelatin is increased, the crosslinked material becomes resistant to swelling, yet retains considerable elasticity and high adhesive strength. The reagents are not cytotoxic at the concentration used in the photopolymerisation reaction. When tested in vivo in sheep lung, the photopolymerised gelatin effectively sealed a wound in lung tissue from blood and air leakage, was not cytotoxic and did not produce an inflammatory response. The elastic properties, thermal stability, speed of curing and high tissue adhesive strength of this photopolymerised gelatin, offer considerable improvement over current surgical tissue sealants. [ABSTRACT FROM AUTHOR]
- Published
- 2010
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9. Honeybee silk: Recombinant protein production, assembly and fiber spinning
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Weisman, Sarah, Haritos, Victoria S., Church, Jeffrey S., Huson, Mickey G., Mudie, Stephen T., Rodgers, Andrew J.W., Dumsday, Geoff J., and Sutherland, Tara D.
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RECOMBINANT proteins , *FIBERS , *HONEYBEES , *BIOMEDICAL materials , *ESCHERICHIA coli , *BIOMIMETIC chemicals - Abstract
Abstract: Transgenic production of silkworm and spider silks as biomaterials has posed intrinsic problems due to the large size and repetitive nature of the silk proteins. In contrast the silk of honeybees (Apis mellifera) is composed of a family of four small and non-repetitive fibrous proteins. We report recombinant production and purification of the four full-length unmodified honeybee silk proteins in Escherichia coli at substantial yields of 0.2–2.5 g/L. Under the correct conditions the recombinant proteins self-assembled to reproduce the native coiled coil structure. Using a simple biomimetic spinning system we could fabricate recombinant silk fibers that replicated the tensile strength of the native material. [Copyright &y& Elsevier]
- Published
- 2010
- Full Text
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