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  • Chemical Engineering  (68)
  • Wiley-Blackwell  (68)
  • Annual Reviews
  • 1990-1994  (68)
  • 1980-1984
  • 1955-1959
  • 1990  (68)
  • 1
    Electronic Resource
    Electronic Resource
    Enhancing adhesion by ion beam-induced atomic mixing at the interface between copper film and polyimide substrate (1990)
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 30 (1990), S. 137-141 
    Details
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Ion beam mixing was used to improve the adhesion between deposited Cu film (400 Å) and polyimide (PI) substrate. Ar+ ion with the energy levels between 180 and 200 keV, and the dose between 1014 to 4 × 1016 ions/cm2 were used. The surface analyses were carried out by Rutherford Backscattering Spectroscopy (SEM). RBS analysis, using 2 MeV He+ ions, showed mixing of Cu and FI and the mixing depended on the Ar+ energy and dose. The X-ray study showed a very broad halo for deposited Cu film but the (111) peak appeared after the Ar+ implantation and the peak increased with Ar+ ion dose. Optical micrographs showed that Cu film formed circular bubbles after many thermal cycles when adhesion was poor and fracture cracks when adhesion was good.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pen.760300302
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  • 2
    Electronic Resource
    Electronic Resource
    Characterization and processing of blends of polyethylene terephthalate with several liquid crystalline polymers (1990)
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 30 (1990), S. 519-526 
    Details
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Blends of an engineering thermoplastic, poly(ethylene terephthalate) (PET), and two liquid crystalline polymers (LCPs) viz., copolyesters of PET and parahydrox-ybenzoic acid (PHB) in 40/60 mole percent (LCP60) and in 20/80 mole percent (LCP80) were prepared. A blend of LCP60 and LCP80 in 50/50 weight percent (LCP60-80) was blended with PET. Both flat films and rods were extruded and their properties examined. The morphology of the films investigated using Scanning Electron Microscopy (SEM) revealed that the LCP phase remained as dispersed droplets in the PET matrix. In spite of the lack of fibrillation in these films, the mechanical properties were enhanced to some extent with a maximum at 10 weight percent of the LCP phase. However, in the case of the rods thin fibrils of the LCP phase of the order of 1 μm in diameter were observed provided the composition of the LCP was 20 weight percent or greater. This success In achieving fibrillation is through to be due to the extensional flow fields present at the entrance of the capillary die and the fact that a short L/D ratio die was used. Differential Scanning Calorimetry (DSC) thermograms of the extruded films indicated that the LCP phase may act as a nucleating agent for the crystallization of PET. Rheology of the blends revealed that the complex viscosity of the blends is not much different from that of pure PET. This is attributed to the partial miscibility of the two components. Based on the DSC results and residence times in the extruder, it is concluded that no significant transesterification reactions appear to have: taken place in the blends. The rheology is studied further with respect to the cooling behavior of the pure components and factors important to the fibrillation of the LCP phase and the formation of in-situ reinforced composites are discussed.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pen.760300904
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  • 3
    Electronic Resource
    Electronic Resource
    Thermomechanical properties of 1C molding compoundsPresented at the Annual Meeting of American Institute of Chemical Engineers in San Francisco, California on November 6, 1989. (1990)
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 30 (1990), S. 609-617 
    Details
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Eight commercial semiconductor grade epoxy compounds that are used to encapsulate 1C (integrated circuit) devices have been evaluated for their ability to minimize the development of thermal stresses which can cause failure during device temperature cycling. Thermal expansion, dynamic modulus and adhesion studies are used to describe the mechanical interaction between the plastic package and the silicon device it surrounds. A “figure of merit” is defined for the development of stress on the 1C device as it is cooled after the packaging process. The stress is shown to be proportional to the product of three terms: (αp-αs) Ep (Tanch-T) where αp and αs are the expansion coefficients for the plastic and silicon, respectively, Ep is the modulus of the epoxy and Tanch is the temperature at which the epoxy becomes anchored to the silicon device during transfer molding. In addition, the importance of good adhesion between the epoxy encapsulant and the silicon device to prevent package cracking has been demonstrated by finite element analysis and a novel adhesion test.
    Additional Material: 16 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pen.760301008
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  • 4
    Electronic Resource
    Electronic Resource
    Comments on “fracture toughness of impact modified polymers based on the J-integral” (1990)
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 30 (1990), S. 1341-1344 
    Details
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: In (1), Narisawa and Takemori examined the physical interpretations and some experimental techniques of the J-Integral (ASTM E813-81) as applied to toughened polymers. Their results and conclusions are reexamined and discussed in terms of recent developments in J testing.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pen.760302102
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  • 5
    Electronic Resource
    Electronic Resource
    Upgrading of solvent extracted Athabasca Bitumen by membrane ultrafiltration (1990)
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 36 (1990), S. 1279-1282 
    Details
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/aic.690360821
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  • 6
    Electronic Resource
    Electronic Resource
    Thermodynamics of Lewis acid-base mixtures (1990)
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 36 (1990), S. 1851-1864 
    Details
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: The associated perturbed-anisotropic-chain theory (APACT) has been applied to treat multicomponent mixtures, in which components exhibit Lewis acid-base interactions. Mixtures of amphoteric molecules (such as alcohols), acidic molecules (such as chloroform), and basic molecules (such as ketones) as well as nonassociating components (diluents) are treated. The acid-base version of the perturbed-anisotropic-chain theory (ABPACT) is a closed form equation of state that takes into account explicitly dispersion interactions, polar interactions, and hydrogen bonding interactions between components that self-associate or solvate. The equation fits binary VLE mixtures quite accurately. Calculated results also are compared with those obtained from the Peng-Robinson equation of state, UNIFAC and the original APACT. In all cases where there are mixtures of associating components, the ABPACT gives a better fit of experimental data than these other equations.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/aic.690361209
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  • 7
    Electronic Resource
    Electronic Resource
    The reaction-independence of mixing coefficients in fixed-bed reactors (1990)
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 36 (1990), S. 1449-1451 
    Details
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/aic.690360920
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  • 8
    Electronic Resource
    Electronic Resource
    Solidification behavior and recovery kinetics of liquid crystalline polymers (1990)
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 30 (1990), S. 989-995 
    Details
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The supercooling behavior of three thermotropic liquid crystalline polymers (TLCP's), 60 mole% p-hydroxybenzoic acid and 40 mole% poly(ethyleneterephthalate), 60/40 PHB/PET, 80 mole% p-hydroxybenzoic acid and 20 mole% poly(ethyleneterephthalate), 80/20 PHB/PET and a copolyester of 73 mole% p-hydroxybenzoic acid and 27 mole% of 2-hydroxy-6-naphthoic acid, Vectra A900, was studied by means of both rheological and thermal methods. 60/40 PHB/PET and Vectra A900 exhibited a degree of supercooling as high as 80°C while there was only 20°C of supercooling for 80/20 PHB/PET. The degree of supercooling for the blends of 60/40 PHB/PET and 80/20 PHB/PET also decreased with the increase in 80/20 PHB/PET content. The increase in G′ as the temperature decreased was more gradual for 60/40 PHB/PET and Vectra A900 than that for 80/20 PHB/PET, which was beneficial from a processing point of view. The solidification of the LCP melt was attributed to both the crystallization and the freezing of the mesophase. The degree of crystallinity for all three TLCP's was very small, less than 5%, as measured by the DSC. It was found that both 60/40 PHB/PET and Vectra A900 showed an induction period of a few minutes during solidification while 80/20 PHB/PET solidified continuously at the test temperature. Therefore, 60/40 PHB/PET and Vectra A900 seem to be more suitable for use in processes such as blow molding and film blowing than 80/20 PHB/PET.
    Additional Material: 16 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pen.760301608
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  • 9
    Electronic Resource
    Electronic Resource
    Impact modification of styrene-acrylonitrile copolymers by methyl methacrylate grafted rubbers (1990)
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 30 (1990), S. 1373-1381 
    Details
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Monodisperse methyl methacrylate grafted latex rubber (MMA-g) particles (0.12-0.13 µm) have been used for the impact toughening of a series of styrene-acrylonitrile (SAN) copolymers of varied AN content. It was found that the MMA-g particles are most effective in toughening SANs containing about 25 to 34% AN. Mechanical properties, interphase adhesion, mechanical dilatometry, and phase morphology by transmission electron microscopy were determined on blends containing 20-30% rubber. Also, the miscibility range of SANs and poly(methyl methacrylate) (PMMA) graft was considered in attempting to analyze the relationships between the mechanical properties and the characteristic features of the blends. Issues relating the impact strength and deformation mechanisms, interphase adhesion, and particle morphology are discussed. It appears that the high impact strength of some of the blends may be caused primarily by certain morphological features such as particle clustering or small interparticle distances. Thus, craze initiation, shear yielding, and significant matrix deformation may all contribute to the overall ductility of the blend.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pen.760302107
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  • 10
    Electronic Resource
    Electronic Resource
    The interface in binary mixtures of polymers containing a corresponding block copolymer: Effects of industrial mixing processes and of coalescencePresented in part at the Annual Meeting of AIChE, Symposium ‘8A’ on Polymer Engineering and Science. New York, November 18, 1987, and at IMRI-NRCC Conference, ‘Polyblends’ 88. April 6, 1988. Montreal. (1990)
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 30 (1990), S. 741-752 
    Details
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: In theories of the minor phase (domain) formation in polyblends rendered as emulsions it is usually assumed that the size and shape of the domains are the result of melt viscosity effects (Taylor, Wu) or viscoelasticity effects (VanOene, Elmendorp) being balanced by interfacial tension. This assumption would predict a monotonic decrease of the domain size to a final limiting size with increasing energy of mixing. However, a systematic study of the dependence of domain morphology on industrial mixing processes which was carried out on a “model” LDPE/PS (2/1) mixture and the related polyalloy (i.e., the same mixture with a corresponding block copolymer as compatibilizer) does not support this expectation. Doirain size was found to go through a minimum as mixing energy was increased. A similar minimum was seen in data on specific volume of the melt vs. mixing energy, which indicates a correlation between melt specific volume and domain size. Calculation of the approximate surface area of the domains using a simple model of domain shape indicated that total interfacial energy in the polyblend and/or polyalloy is a trivial part of the mixing energy introduced. These calculations also indicated that if compatibilizer was located entirely at the interface, the surface layer would have a thickness of about 90 nm. Some micrographs seem to show such a surface layer. We propose that an abrasion mechanism is responsible for the early stage of the dispersion process, and that the final domain size may be controlled by a dispersion-coalescence equilibrium. This is compared with the theories of final particle size proposed by VanOene and Wu.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pen.760301207
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