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Polyamide 6/layered double hydroxide composites : an investigation of their mechanical and thermal properties.Zwane, Recardo Derely Sibusiso. January 2014 (has links)
M. Tech. Polymer Technology / Reduced carbon dioxide emissions, improved fuel economy and better performance are just but a few pressures that have continued to define the automotive industry, globally. Low-cost and light weight materials have continually been used to replace metals as conventional raw materials in the manufacturing of automotives. Polymers have been a material of choice for meeting these demands; mainly due to their versatility, ease of processing and giving the manufacturers an option of parts integration. The industry has experienced remarkable product improvement from metal-to-plastic conversion and hence, further the plastic-to-plastic refinement of vehicle parts, from the interior, to body panels and to engine parts. Glass-filled polyamide 66 (PA66) composites have been extensively used in the production of engine components since post World War II era, which has paved the way for glass-filled polyamide 6 (PA6) composites, which has a lower melting point than PA66, to be used in technical applications for vehicle engine parts. This work attempts to investigate the use of layered double hydroxide (LDH) clay, the so called "anionic" clays for the preparation of PA6/LDH composites. In this study, PA6/LDH composites were prepared and the effect of organic modification of magnesium (Mg)-aluminium (Al) LDH clay was investigated. The aim of this research was to investigate the effect of organically modified and "unmodified" commercial Mg-Al LDH on the thermal, mechanical and physical properties of PA6 composites.
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Effect of processing parameters on morphology and mechanical properties of carbon/PEEK (APC2) compositeShukla, Jay G. January 1988 (has links)
No description available.
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On-line consolidation of thermoplastic powder fusion coated filamentsRammoorthy, Madhusudhan 12 1900 (has links)
No description available.
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Model development for the electrostatic fluidized bed powder coating processDeBenedictis, Mach Austin 05 1900 (has links)
No description available.
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Modeling the processing science of thermoplastic composite tow prepreg materialsYang, Heechun 12 1900 (has links)
No description available.
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Performance of jointed fibre-glass composites /Juwono, Ariadne Lakshmidevi. Unknown Date (has links)
Thesis (M.Eng.)--University of South Australia, 1995.
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Polyurethane organosilicate nanocomposites for novel use as biomaterialsStyan, Katie, Graduate School of Biomedical Engineering, Faculty of Engineering, UNSW January 2006 (has links)
Polymer organosilicate nanocomposites have attracted significant attention over the last decade due to improved mechanical, thermal, and barrier properties. Several nanocomposite researchers have recognised potential for biomedical applications, however none have conducted biological investigations. In this project, the predicted ability of the organosilicate to enhance biostability, modulate the release of included drugs, and confer biofunctionality and control over the host response, were assessed as the three primary hypotheses. The studies were conducted with the objective being employment as urinary device biomaterials. Of prime importance was that no detrimental change in cytocompatibility was resultant. Biomedical thermoplastic elastomeric polyurethane organosilicate nanocomposites were prepared from poly(ether)urethane of 1000g/mol poly(tetramethylene oxide) polyol, 4,4??? diphenylmethane diisocyanate, and 1,4 butanediol chain extender chemistry, and various organosilicates with loadings from 1w% to 15w%, using a solution casting technique. Initially, partially exfoliated nanocomposites were produced using a commercially available organosilicate, Cloisite?? 30B. These nanocomposites displayed several advantageous properties, namely i) significant anti-bacterial activity, reducing S. epidermidis adherence after 24h to ~20% for a 15w% organosilicate loading, ii) enhanced biostability, with a 15w% organosilicate loading displaying only slight degradation after a 6 week subcutaneous in vivo ovine implantation, and iii) static modulation of model drug release as a factor of drug properties and organosilicate loading. The former was attributed to the Cloisite?? 30B quaternary ammonium compound, while the latter two were likely primarily barrier effect related and due to changes to poly(ether)urethane permeability. Electrostatic and chemical interactivity between drug and organosilicate was also implicated in the observed drug release modulation. Unfortunately, a lack of in vitro cytocompatibility and poor in vivo inflammatory response will limit in vivo use. Utilising bioinert 1-aminoundecanoic acid as an alternative organic modification, cytocompatible intercalated nanocomposites were produced thus likely allowing in vivo nanocomposite use and exploitation of the barrier effect related properties. However, these nanocomposites were not antibacterial. Variation of the organic modification and/or use of co-modification were viable means of modulating host response and biofunctionality, however nanoscale dispersion of co-modified silicate was poor. Use of nanocomposite technology was concluded beneficial to existing biomaterials, and specifically to biomaterial application as urinary catheters / stents.
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The investigation of novel polymer-photochromic conjugatesSuch, Georgina, School of Chemical Engineering & Industrial Chemistry, UNSW January 2005 (has links)
My research has focussed on the development of a technique to tailor photochromic switching rates by creating a customised local environment for the dye within an otherwise rigid host matrix. Living radical polymerisation offers the potential to design such a system. A living radical initiator based on a spirooxazine compound was used to polymerise a polymer chain of well controlled molecular weight and polydispersity. This technique facilitated the construction of a conjugate with every photochromic moiety convalently attached to a polymer chain with uniform characteristics. The photochromic behaviour of these new polymer-spirooxazine conjugates were investigated in a cross-linked polymer matrix with a Tg of approximately 120??C. It is well known that photochromic switching is susceptible to local environment effects such as rigidity, free volume and polarity.1, 2 The goal of these systems was to create a uniform local environment which would facilitate controlled changes in the photochromic switching rates. The photophysical investigation of these systems demonstrated the success of this technique. The photochromic rates were directly related to the characteristics of the polymer conjugate. It was postulated the conjugates acted as a customised local environment for the photochromic moiety, encapsulating it from the host matrix. Consequently systematic tailoring of the photochromic switching rates was achieved by changes in the characteristics of the attached polymer. To our knowledge this is the first technique to control local environment of a photochromic compound and thus the first example of systematic tuning of photochromic switching rates. Throughout this research, several characteristics of the attached polymer were modified to give a series of rules for the tuning of photochromic switching rates using this technique. The largest variation in switching speed is achieved through variation of Tg. A range of photochromic rates from extremely slow to near solution-like can be easily achieved. The necessary variations in Tg can be achieved easily using living radical polymerisation techniques. The use of different homopolymers, block and random copolymers were all demonstrated successfully in this work. For finer tuning of the photochromic rates, changes in chain length can be used. It was also found the best living radical polymerisation method for this work was ATRP due to the bulky or incompatible halogen which contributed to efficient encapsulation. However this endgroup effect is only important in systems which do not have a low Tg component. The incorporation of such a component overrides all other contributions to the overall behaviour.
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Drag reduction in pipe flows with polymer additives /Grabowski, Daniel W. January 1990 (has links)
Thesis (M.S.)--Rochester Institute of Technology, 1990. / Includes bibliographical references (leaf 80).
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Bulk and interfacial effects on density in polymer nanocompositesSahu, Laxmi Kumari. D'Souza, Nandika Anne, January 2007 (has links)
Thesis (Ph. D.)--University of North Texas, May, 2007. / Title from title page display. Includes bibliographical references.
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