• Refine Query
  • Source
  • Publication year
  • to
  • Language
  • 1
  • 1
  • Tagged with
  • 4
  • 4
  • 4
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • About
  • The Global ETD Search service is a free service for researchers to find electronic theses and dissertations. This service is provided by the Networked Digital Library of Theses and Dissertations.
    Our metadata is collected from universities around the world. If you manage a university/consortium/country archive and want to be added, details can be found on the NDLTD website.
1

Homogenization and incompatibility fields in finite strain elastoplasticity

Clayton, John D. 12 1900 (has links)
No description available.
2

In situ composites of compatibilized polypropylene/liquid crystalline polymer blends

O'Donnell, Hugh J. 05 February 2007 (has links)
Methods of processing polypropylene (PP)/ liquid crystalline polymer blends to obtain high mechanical properties from injection molded samples were investigated in this dissertation. Three liquid crystalline polymers (LCPs), two liquid crystalline (LC) copolyesters and one LC poly(ester-amide), were used. The PP/LCP blends were compatibilized with a maleic anhydride grafted polypropylene (MAP) to enhance the mechanical properties. The effect of increasing MAP content on the mechanical properties, morphology, and interfacial tension of injection molded tensile bars and plaques made from blends with 30 wt% LCP was investigated. It was determined that MAP enhances both the tensile strength and modulus, but the tensile strength is increased to a greater degree than the tensile modulus. For the LC copolyesters, the tensile strength appeared to reach a maximum while for the LC poly(ester-amide) the tensile strength increased without limit in the range of MAP contents studied. Simultaneously, a finer dispersion was created as the MAP content was increased. Calculation of the interfacial tension from contact angle measurements indicated that the interfacial tension decreased as MAP was added to the PP matrix. Analysis of the MAP concentration after blending indicated that MAP did not react with the LCP, but enhanced tensile properties resulted from physical interaction such as hydrogen bonding. This mechanism is consistent with the greater property improvements found in the LC poly(ester-amide) blends where the amide group is expected to undergo stronger hydrogen bonding than the ester group. Analysis of the injection molding of these blends found that heat transfer and solidification significantly affected the flexural modulus of these blends. Injection molding conditions such as fill time, mold thickness, mold temperature and melt temperature were investigated in three molds of different thicknesses. Different processing relationships were found between the LC copolyesters and the LC poly(ester-amide). For the former LCP blends, the highest moduli were obtained from the thinnest mold in a manner parallel to that of the moduli of neat LCPs. For the latter LCP blends, the highest moduli were obtained in the intermediate thickness mold. The differences between the copolyester and LC poly(ester-amide)s processing / property relationships were related to the melt rheology of the LCPs. For the LC copolyesters, maximum mechanical properties were obtained when the melt temperature was selected so that the storage and loss moduli of the LCP were nearly equal. This equality of storage and loss moduli could not be achieved with the LC poly(ester-amide). In addition, upon cooling, the storage and loss moduli of the LC poly(ester-amide) indicated that rapid solidification occurred while a much lower rate of solidification was indicated for the LC copolyesters. In addition the mechanical properties were sensitive to the rate of cooling as indicated by the Graetz number. It was speculated that attainment of the highest mechanical properties was related to the LCP being deformed during the filling stage followed by rapid solidification of the LCP morphology upon cessation of flow. / Ph. D.
3

Development of nano-graphene cementitious composites (NGCC)

Ilyas, Muhammad January 2016 (has links)
Ordinary Portland cement (OPC) is the main constituent of concrete works as a principal binder for aggregates and intrinsically transmits the brittleness into concrete through the formation of hydration crystals in the cement microstructure. A number of nano cementitious composites were developed in recent years to offset the brittleness with newly discovered nanomaterials and the most prevalent among those is the graphene oxide (GO). The main objective of this PhD research work is to develop nano graphene cementitious composites (NGCC) using low cost, two dimensional (2D) graphene nanoplatelets (GNPs) and one dimensional (1D) graphited carbon nanofibres (GCNFs) with unique conical surface morphology. The GNPs were sourced synthesised in an environmental friendly way via plasma exfoliation whereas, GCNFs were manufactured through catalytic vapour grown method. The project further investigated the effect of these nanomaterials in regulating the distinctive microstructure of cement matrix leading to enhance its mechanical properties. Three different types of high-performance NGCC namely NGCC-Dot, NGCC-Fnt and NGCC-CNF, are developed by activating pristine GNPs (G-Dot), functionalised GNPs (G-Fnt) and graphited nanofibers (G-CNFs) into the cement matrix respectively. It is found through various characterization and experimental techniques that both GNPs and GCNFs regulated the cement microstructure and influenced the mechanical properties of NGCC uniquely. A remarkable increase in the flexural and the tensile strength of newly developed NGCC has been achieved and that could be attributed to the formation of distinctive microstructure regulated by catalytic activation of these nanomaterials. The shape (1D, 2D) and unique morphology of these nanomaterials played a vital role in the mechanism of crystal formation to regulate the cement microstructure. Based on the observations of test results and comprehensive characterization, the possible mechanisms of crystal formation and development of distinctive microstructure of NGCC has been established which has then proceeded to the development of a physical model for NGCC development.
4

Characterization and Design of Liquid Crystal Polymer (LCP) Based Multilayer RF Components and Packages

Thompson, Dane C. 11 April 2006 (has links)
This thesis discusses the investigation and utilization of a new promising thin-film material, liquid crystal polymer (LCP), for microwave and millimeter-wave (mm-wave [>30 GHz]) components and packages. The contribution of this research is in the determination of LCP's electrical and mechanical properties as they pertain to use in radio frequency (RF) systems up to mm-wave frequencies, and in evaluating LCP as a low-cost substrate and packaging material alternative to the hermetic materials traditionally desired for microwave circuits at frequencies above a few gigahertz (GHz). A study of LCP's mm-wave material properties was performed. Resonant circuit structures were designed to find the dielectric constant and loss tangent from 2-110 GHz under both ambient and elevated temperature conditions. Several unique processes were developed for the realization of novel multilayer LCP-based RF circuits. These processes include thermocompression bonding with tight temperature control (within a few degrees Celsius), precise multilayer alignment and patterning, and LCP laser processing with three different types of lasers. A proof-of-concept design that resulted from this research was a dual-frequency dual-polarization antenna array operating at 14 and 35 GHz. Device characterization such as mechanical flexibility testing of antennas and seal testing of packages were also performed. A low-loss interconnect was developed for laser-machined system-level thin-film LCP packages. These packages were designed for and measured with both RF micro-electromechanical (MEM) switches and monolithic microwave integrated circuits (MMICs). These research findings have shown LCP to be a material with uniquely attractive properties/capabilities for vertically integrated, compact multilayer LCP circuits and modules.

Page generated in 0.5965 seconds