The objective of this thesis is to design RF circuits using silicon-germanium (SiGe) heterojunction bipolar transistors (HBTs) for communication system. The packaging effect for the SiGe chip using liquid crystal polymer (LCP) is presented and methodology to derive the model for the package is discussed. Chapter 1, we discuss the overview and benefits of SiGe HBT technology in high frequency circuit design. Chapter 2 presents the methodology of the low noise amplifier (LNA) design and discusses the trade-off between the noise and gain matching. The technique for achieving simultaneous noise and gain matching for the LNA is also presented. Chapter 3 presents an L-band cascaded feedback SiGe low noise amplifier (LNA) design for use in Global Position System (GPS) receivers. Implemented in a 200 GHz SiGe BiCMOS technology, the LNA occupies 1 x 1 millimeter square (including the bondpads). The SiGe LNA exhibits a gain greater than 23 dB from 1.1 to 2.0 GHz, and a noise figure of 2.7 to 3.3 dB from 1.2 to 2.4 GHz. At 1.575 GHz, the 1-dB compression point (P1dB) is 1.73 dBm, with an input third-order intercept point (IIP3) of -3.98 dBm. Lastly, Chapter 4 covers the packaging techniques for the SiGe monolithic integrated circuit (MMIC). We present the modeling of a liquid crystal polymer (LCP) package for use with an X-band SiGe HBT Low Noise Amplifier (LNA). The package consists of a 2 mil LCP laminated over an embedded SiGe LNA, with vias in the LCP serving as interconnects to the LNA bondpads. An accurate model for the packaging interconnects has been developed and verified by comparing to measurement results, and can be used in chip/package co-design.

No description available.

Thesis (Ph. D.)--University of Washington, 1998. / Vita. Includes bibliographical references (leaves [89]-102).

Includes bibliographical references (p. 162-177).

Thesis (Ph. D.)--Electrical and Computer Engineering, Georgia Institute of Technology, 2006. / Swaminathan, Madhavan, Committee Chair ; Cressler, John D., Committee Co-Chair ; Kenney, Stevenson J., Committee Member ; Peterson, Andrew, Committee Member ; Durgin, Gregory, Committee Member ; Sitaraman, Suresh, Committee Member.

Molecular reinforcement through in-situ polymerization of liquid crystalline epoxies (LCEs) and a non-liquid crystalline epoxy has been investigated. Three LCEs: diglycidyl ether of 4,4'-dihydroxybiphenol (DGE-DHBP) and digylcidyl ether of 4-hydroxyphenyl-4"-hydroxybiphenyl-4'-carboxylate (DGE-HHC), were synthesized and blended with diglycidyl ether of bisphenol F (DGEBP-F) and subsequently cured with anhydride and amine curing agents. Curing kinetics were determined using differential scanning calorimetry (DSC). Parameters for autocatalytic curing kinetics of both pure monomers and blended systems were determined. The extent of cure for both monomers was monitored by using Fourier transform infrared spectroscopy (FT-IR). The glass transitions were evaluated as a function of composition using DSC and dynamic mechanical analysis (DMA). The results show that the LC constituent affects the curing kinetics of the epoxy resin and that the systems are highly miscible. The effects of molecular reinforcement of DGEBP-F by DGE-DHBP and DGE-HHC were investigated. The concentration of the liquid crystalline moiety affects mechanical properties. Tensile, impact and fracture toughness tests results are evaluated. Scanning electron microscopy of the fracture surfaces shows changes in failure mechanisms compared to the pure components. Results indicate that mechanical properties of the blended samples are improved already at low concentration by weight of the LCE added into epoxy resin. The improvement in mechanical properties was found to occur irrespective of the absence of liquid crystallinity in the blended networks. The mechanism of crack study indicates that crack deflection and crack bridging are the mechanisms in case of LC epoxy. In case of LC modified epoxy, the crack deflection is the main mechanism. Moreover, the effect of coreacting an epoxy with a reactive monomer liquid crystalline epoxy as a matrix for glass fiber composites was investigated. Mechanical properties of the modified matrix were determined by tensile, flexural and impact testing. The improvement in toughness of the bulk matrix by the addition of a LCEs is seen also in the composites. The improvement is related to the enhancement of adhesion between the glass fibers and the matrix.

Thermoplastic polyimides (TPIs) exhibit high glass transition temperatures (Tgs), which make them useful in high performance applications. Amorphous and semicrystalline TPIs show sub-Tg relaxations, which can aid in improving strength characteristics through energy absorption. The a relaxation of both types of TPIs indicates a cooperative nature. The semicrystalline TPI shows thermo-irreversible cold crystallization phenomenon. The polymer liquid crystal (PLC) used in the blends is thermotropic and with longitudinal molecular structure. The small heat capacity change (ACP) associated with the glass transition indicates the PLC to be rigid rod in nature. The PLC shows a small endotherm associated with the melting. The addition of PLC to the semicrystalline TPI does not significantly affect the Tg or the melting point (Tm). The cold crystallization temperature (Tc) increases with the addition of the PLC, indicating channeling phenomenon. The addition of PLC also causes a negative deviation of the ACP, which is another evidence for channeling. The TPI, PLC and their blends show high thermal stability. The semicrystalline TPI absorbs moisture; this effect decreases with the addition of the PLC. The absorbed moisture does not show any effect on the degradation. The addition of PLC beyond 30 wt.% does not result in an improvement of properties. The amorphous TPI + PLC blends also show the negative deviation of ACP from linearity with composition. The addition of PLC causes a decrease in the thermal conductivity in the transverse direction to the PLC orientation. The thermomechanical analysis indicates isotropic expansivity for the amorphous TPI and a small anisotropy for the semicrystalline TPI. The PLC shows large anisotropy in expansivity. Even 5 wt. % concentration of PLC in the blend induces considerable anisotropy in the expansivity. Thus, blends show controllable expansivity through PLC concentration. Amorphous TPI + PLC blends also show excellent film formability. The amorphous TPI blends show good potential for applications requiring high thermal stability, controlled expansivity and good film formability.

This work is concerned with the processing of pellets of polypropylene (PP) containing pregenerated microfibrils of thermotropic liquid crystal polymers (TLCPs), referred to as microcomposites. The processing methods used are injection molding, sheet extrusion, and extrusion blow molding. The TLCPs used are HX6000 and Vectra A950. The microcomposites are produced by drawing strands of PP and TLCPs generated by means of a novel mixing technique and pelletizing the strands. The work was undertaken in an effort to improve on the properties observed for in situ composites in which the TLCP fibrils are generated in elongational flow fields that occur during processing. In situ composites usually exhibit highly anisotropic mechanical properties and the properties do not reflect the full reinforcing potential of the TLCP fibers. Factors considered include the effect of in situ composite strand properties on the properties of the injection molded composite, the melt temperature used in injection molding, TLCP concentration, and the melt temperature of the TLCP. It was found in this work that microcomposites can be processed by means of injection molding, sheet extrusion, and extrusion blow molding. It was necessary to process the materials at low temperatures to maintain the TLCP fibrils. However, HX6000, the higher melting TLCP allowed higher processing temperatures than Vectra A. When the TLCP fibrils were maintained, the properties of the TLCP reinforced composites did show reduced anisotropy as compared to an in situ composite. The tensile strength of the composites produced by all three methods was about equal. The modulus of the injection molded composites was slightly higher than that of the composite sheets, but the composite sheets showed a lower degree of anisotropy. In all three processing methods the modulus of the TLCP reinforced composite was a function of the modulus of the in situ composite strand used to produce the microcomposite. Therefore, it is recommended that to improve the properties of the microcomposites the properties of the in situ composite strands should be improved. Furthermore, the mechanical properties of the composites increased with increasing TLCP composition. To provide a basis of comparison the properties of the extruded sheets and the injection molded composites were compared to both the predictions of composite theory and the properties of glass reinforced composites. It was found that the modulus of the 10 wt% composites approached the predictions of composite theory, but at higher TLCP loadings the modulus showed negative deviations from the predictions of composite theory. This is believed to be the result of a reduction of fiber aspect ratio due to poor fiber distribution and fiber breakup. The modulus of the TLCP reinforced composites was about the same as the modulus of the glass reinforced composites produced by both sheet extrusion and injection molding. The tensile strengths were slightly lower than that of the glass reinforced composites. It is expected that as the modulus and strength of the reinforcing TLCP fibrils are improved the properties of the TLCP reinforced composites should exceed those of glass reinforced composites. It was concluded that the processing of microcomposites is a viable means of producing composites based on TLCPs and thermoplastics with good mechanical properties and low degrees of mechanical anisotropy. / Ph. D.

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.

The overall objectives of this work were to improve a dual extrusion process (DEP) which is used to blend thermotropic liquid crystalline polymers (TLCPs) with thermoplastics, determine the mechanism by which TLCP morphology is developed in the DEP and to determine the optimal properties possible in composite materials generated from the blends. The DEP consists of two single screw extruders within which the TLCP and matrix material are plasticated separately. The two continuous polymer streams are joined and then mixed in a series of static mixing elements. Composite materials were formed from pelletized pregenerated strands by processing at temperatures below the melting point of the TLCP. The DEP was improved by the addition of a gear pump to the TLCP stream, a multiple port phase distribution system, static mixing design, minimization of residence time, die design, and introduction of thermal control over the entire strand production process. The TLCP material was introduced into the matrix phase by means of a multiple port phase distribution system which injected 12 individual TLCP streams parallel to the flow direction of the matrix stream. This design resulted in improvements in the axial continuity of the TLCP phase during mixing and improved radial mixing as compared with a simple T-injection system. Both Kenics and Koch static mixer designs were evaluated in this investigation and it was found that the use of either could produce similar mechanical property enhancement in the resulting blends provided that an excessive number of elements were not used. Furthermore, it was found that the most stable strand materials were formed when the die was designed with respect to the flow exiting the static mixer elements. For example, a dual strand die with each capillary having an L/D ratio of 1 produced the most stable strands when used with the Kenics mixing elements. Finally, it was found that drawing the molten blend strand in a vertical drawing chimney provided a favorable thermal environment and resulted in much higher draw ratios and high mechanical properties of the strand. The other objectives of this work including the development of morphology and composite materials produced from pregenerated strands is presented in two manuscripts formatted for submission to appropriate journals. Detailed abstracts dealing with these two topics are included therein. / Master of Science