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  • 1
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 19 (1973), S. 552-558 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: An experimental investigation of the penetration distance required for complete condensation of a submerged turbulent vapor jet injected into a quiescent liquid bath of the same material was made. The bath was maintained in a subcooled condition at a temperature below the boiling temperature of the liquid at the bath pressure. The experiments were limited to choked injector Hows with the penetration regime such that buoyancy effects are negligible. Tests were run for water, ethylene glycol, and iso-octane over a range of flow rates and bath pressures. A theoretical expression for the vapor penetration distance was developed utilizing a variable density single fluid model for the two-phase flow, with the turbulent mixing process treated by an entrainment law. Corrections for the external expansion of the choked flow beyond the injector exit were also determined. This model was found to correlate the results of both the present experiments and those of earlier investigators over a wide range of operating conditions and injector geometries.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 18 (1972), S. 548-553 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: An experimental investigation was made of the lenght of the turbulent vapor cavity formed by a steam jet discharging into a subcooled liquid water both. The experiments considered both constant area and convergent-divergent steam injectors of various external geometries. The tests were conducted with the bath at atmospheric pressure, bath temperatures in the range 301-358K, injector exit diameters in the range 0.00040-0.0112 m, for choked injector flows having mass velocities in the range 332-2050 kg/m2.s. These conditions yielded injector exit Reynolds numbers from 2 to 150 × 104. Over this range a correlation was developed to yield the length of the vapor cavity as a function of the injector diameter, exit mass velocity, and a driving potential for the condensation process. The heat transfer coefficients for this condensation process were found to be significantly greater than those encountered in turbulent film condensation processes in the vicinity of tubes and walls.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 11 (1972), S. 899-912 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The isometric tensile stress generation observed when collagen fibers are immersed in aqueous solutions of lithium bromide ranging in molar concentration up to 7 was studied at 23°C. The reverse process, namely, isometric stress relaxation of the fiber occurring by subsequent immersion in distilled water, was also studied. We find that the data in the region of LiBr concentration up to about 2.5 moles/liter are adequately represented by a superposition integral \documentclass{article}\pagestyle{empty}\begin{document}$$ \sigma (t) = \int_{ - \infty }^\infty {K(t - \tau )} \frac{{dc(\tau )}}{{d\tau }}\,d\tau $$\end{document} where σ(t) is the time-dependent stress generated by the collagen fiber held at fixed length, c(t) is the history of LiBr molar concentration, and K(t) is the isometric contractility function, expressed as stress per unit salt concentration. We conclude that, within a limited range of salt concentration, a collagen fiber in a LiBr bath behaves as if it were a linear, time-invariant system defined mechanochemically by a single function K(t) which depends on the structural characteristics of the fiber while being independent of salt concentration. An analysis is presented of isometric mechanochemical data obtained under conditions of equilibrium by other workers who studied the behavior of collagen fibers in aqueous solutions either of urea, LiBr, or KCNS. The analysis shows that these independent (equilibrium) data confirm the linarity of the relation between isometric contractile stress and salt concentration on which our superposition integral representation is based. We also find that the asymptotic (infinite-time) value of the isometric stress is linearly related to the chemical potential of the salt as well, in agreement with the equilibrium thermodynamic treatment of mechanochemical processes by Katchalsky and Oplatka.
    Additional Material: 7 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 11 (1979), S. 23-44 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The decomposition of C2H6 in Ar was studied by laser-absorption and laser-schlieren measurements of the reaction rate behind incident shock waves with 1300 〈 T 〈 2500°K and 1.1 〈 ρ 〈 4.4 × 10-6 mol/cm3. The experimental profiles were parameterized by suitable measures of reaction progress. Computer simulations using a 14-reaction mechanism were used to compare assumptions about rate constant expressions with the experimental parameters and to investigate the sensitivity of computed parameters to these assumptions. A rate constant expression k(cm3/mol·sec) = 2 × 10111 T-25.26 exp(-80 320/T) was found for the primary dissociation step C2H6 + M = CH3 + CH3 + M under the conditions studied; no difference in rate was discernable between M = Ar and M = C2H6. Rate constant expressions found to be suitable for the remaining reactions of the mechanism, to some of which the computed parameters were sensitive, were in accord with previous proposals. Our results and results from earlier investigations of the primary decomposition reaction, in both forward and reverse directions, were extrapolated, using RRK methods, to obtain low-pressure limiting rate constants and found to be concordant.
    Additional Material: 14 Ill.
    Type of Medium: Electronic Resource
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