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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Biotechnology and Bioengineering 48 (1995), S. 246-256 
    ISSN: 0006-3592
    Keywords: polyethylene glycol ; phosphate ; phase separation ; kinetics ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Phase separation times for polyethylene glycol (PEG)-4000-phosphate aqueous two-phase systems were studied, for small scale (5-g) and large scale (1300-g) systems, as a -function of the stability ratio. Profiles of dispersion height for both large and small scale systems were represented as a fraction of the initial height and were found to be independent of the geometrical dimensions of the separator. Furthermore, by plotting time as a fraction of the initial height the total time of separation can be calculated for a given height of system at a particular stability ratio. This generalization is important for the design of large scale aqueous two-phase separators. Phase separation times were also found to be dependent on which of the phases is continuous. A characteristic change in phase separation time was also observed at the phase inversion point (i.e., where the dispersed phase changes to a continuous phase and vice versa) and this point tends toward higher volume ratios as the tie-line length (TLL) is increased. Furthermore, the phase inversion point at each TLL corresponds to a fixed phosphate concentration. © 1995 John Wiley & Sons, Inc.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 22 (1982), S. 637-644 
    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 order to understand the mechanism of adhesion promotion by organo silane in joints where its chemical reaction with a polymer matrix may be negligible, we studied the role of γ-aminopropyl triethoxy silane (γ-APS) in α-Al2O3/ polyethylene joints. When adsorbed or deposited on α-A12O3/ and moderately dried, γ-APS forms a multimolecular film that is not fully cured. Drying at elevated temperatures for an extended time leads to further curing, resulting in a glassy silane film with a Tg around 108°C, while prolonged dry may cause some degradation. Joint strength is markedly improved by the application of a γ-APS film with a maximum peel strength of 2.3 kg/cm when the silane is applied from a 2 percent aqueous solution. Drying the silane at an elevated temperature prior to joint formation reduces joint strength and also changes the failure mode from cohesive failure through the polyethylene to a mixed mode. Evidence of interdiffusion between γ-APS film and polyethylene at a temperature (149°C) that is above the melting point of polyethylene and the Tg of the silane film was obtained by measuring the Si concentration profile across the interface of the laminate of polyethylene/γ-APS/polyethylene. Diffusion constants in the order of 10-12 cm2/s were obtained, with a teridency toward reduced diffusion as a consequence of extensive drying. DSC results indicate at least partial miscibility of the silane polymer in the amorphous region of polyethylene. It is proposed that the interdiffusion between γ-APS silane film and polyethylene is an important mechanism for adhesion promotion of the joints investigated in this study.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 26 (1986), S. 768-775 
    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 strength and durability in wet environment of aluminum/epoxy/aluminum joints are investigated as a function of structural changes of γ aminopropyltriethoxy silane (γ-APS) primer at the interface. Both dry and wet strengths exhibit strong dependencies on both the thickness and the extent of drying of γ-APS prior to joint formation. Generally, dry strength decreases with increasing thickness of γ-APS primer, and increases with dehydration of γ-APS at any given thickness. Strength retention of the joints after exposure to water at 55°C also improves dramatically when the adsorbed γ-APS is extensively dried. These results are analogous to earlier observations with α-Al2O3/polyethylene joint system. In aluminum joints, porous oxide substrate facilitates the mechanical interlocking mechanism, and its interplay with both the thickness and the extent of cure of γ-APS is analyzed by characterizing the fractured surfaces using scanning electron microscopy (SEM) electron spectroscopy for chemical analysis (ESCA).
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 25 (1985), S. 1171-1178 
    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: Unprimed sapphire/nylon 6 peel joints (2.13 ± 0.27 Kg/cm) are found to be stronger than sapphire/polyethylene joints (0.06 ± 0.02 Kg/cm). Priming the sapphire with γ-aminopropyl triethoxy silane (γ-APS) improves the strength significantly resulting in adherend failure in the nylon. The rate and extent of degradation is lower with priming. The optimal silane thickness is about 1900 Å, obtained with a 0.3 percent γ-APS solution, for a five day exposure to water at 25°C. Peel joints made with 0.3 percent γ-APS film, both dried at 25°C (standard conditions) and dehydrated at 110°C under vacuum, fail cohesively when exposed at 25°C. Increasing the exposure to 55°C in a second step results in strength degradation only with dehydrated films. Lower joint strengths are obtained with five days exposure as compared to one day exposure. However, if the temperature is raised to 65°C the joints primed with standard dried films now begin to degrade and lose 90 percent of their strength in five days. Further, the nylon 6 peel joints made with a 0.3 percent γ-APS film, dehydrated for three days prior to lamination, show 10 times greater wet strengths than the corresponding PE joints. Failure surface analyses by ESCA and SEM suggest that failure locus due to water degradation is within the γ-APS layer and the failure mode is cohesive. Failure mechanics during testing the wet peel joints may also cause a partial interfacial failure mode. The effects of the silane film thickness, dehydration condition, time, and temperature dependence of the peel strength degradation indicates that the structure of the γ-APS layer plays an important role in the promotion and retention of adhesion with a thermoplastic polymer system capable of limited primary interactions through possible interdiffusion with the silane layer.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 24 (1984), S. 493-500 
    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 durability of the joints, consisting of α-Al2O3 primed with γ-aminopropyl triethoxysilane (γ-APS) and polyethylene (PE), in wet environment is investigated as a function of the γ-APS thickness, dehydration of γ-APS prior to joint formation and redrying the joint after a certain exposure. The joint strength measured by 180°s peel is found to decrease with exposure time in wet environment more rapidly in water than in 100 percent RH. With exposure time, the debonded area increases from the edges toward the central area of the joint. Relatively thin γ-APS treatments on α-Al2O3 appear to provide a more durable joint than thicker γ-APS treatments resulting in an optimal thickness in the range of 0.3 ∼ 1 percent γ-APS concentration level. Dehydration of γ-APS leads to more durable joints with an optimal condition found between 1 ∼ 2 days of dehydration at 100°C in vacuum. Regardless of the γ-APS thickness and dehydration history, the failure in the de-bonded area seems to occur by the hydrolysis of γ-APS near the α-Al2O3 side and by the deformation of polyethylene (cohesive failure) in the peeled area, as characterized by SEM and ESCA. The debonded area in the dried joint recovers little strength, but in the central bonded areas, the strength is mostly recovered, characterized by cohesive failure of polyethylene. Diffusion of water in γ-APS near the α-Al2O3 side rather than the PE side can explain at least qualitatively most of the observed trends. The effects of γ-APS thickness and dehydration on the durability in wet environments are compared with those on adhesion promotion in dry environments as well as on their respective failure mode.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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