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  • Chemical Engineering  (73)
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  • 1
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 32 (1986), S. 1169-1175 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: A feasible means for the long-term storage of thermal energy considers the hydration of CaCl2. Differential and integral beds of Celite pellets impregnated with CaCl2 were employed to dehydrate humid air. Experimental studies were used in modeling the behavior of this system, which involved the solution of four partial differential equations. The simultaneous solution of these equations, using a modified Gear's method, yielded information about the temperature and composition distribution of both the air stream and the impregnated pellets. The mathematical solution predicts the time-dependent moving front characterized by a maximum temperature. Predicted and experimental measurements were found to be in good agreement.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 4 (1958), S. 63-68 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Heat and momentum transfer studies have been made for the flow of gases through fixed beds consisting of randomly packed, solid metallic particles. The experimental technique employed in these studies made possible for the first time the procurement of gas-film heat transfer data under steady state conditions and in the absence of mass transfer effects. Electric current passed through the metallic particles of the bed created within the particles a steady generation of heat, which was continuously removed by gases flowing through the bed. Several direct temperature measurements of both gases and solids within the bed made possible the direct calculation of the heat transfer coefficient for the gas film to produce the Colburn heat transfer factor jh, which has been found to correlate with the modified Reynolds number, Reh = √ ApG/[µ(1 - ∊)ϕ]. The shape factor ϕ was established in these studies for cubes and cylinders and was found to be identical to their respective sphericities.Pressure-drop measurements produced a friction factor fk of the Blake type, which yielded separate curves for each shape when correlated with the modified Reynolds number Rem. No simple relationship was found to exist between the heat transfer and friction factors. A single correlation of the pressure-drop data was obtained for the modulus fkoϕn when correlated with a Reynolds number of the type Rem = √ ApG/[µ(1 - ∊)]. The exponent n varies with the particle shape.Experimental runs have been carried out for 3/16, 1/4, 5/16-in. spheres, 1/4 and 3/8-in. cubes, and regular cylinders using hydrogen and carbon dioxide to extend the range of molecular weights beyond that of air, used for the majority of these runs. A particle-size, column-diameter effect was found to exist for both heat and momentum transfer. This effect becomes significant in the low Reynolds region.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 4 (1958), S. 257-262 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: A reduced-state viscosity correlation has been constructed from the available data of the inert gases. For the development of this correlation, the fragmentary experimental data for argon were utilized along the lines proposed for thermal conductivities by Owens and Thodos (21) in order to determine the effect of pressure on viscosity. In addition, the only available low-pressure viscosity data for neon and helium have been incorporated in this correlation to produce for the first time the effect of subatmospheric pressures. This correlation covers the range of pressures included between PR = 40 and PR = 0.015 × 10-4 and extends up to temperatures of TR = 100. It has been found that the effect of subatmospheric pressures on viscosity does not become significant above pressures of 1 mm. of mercury. However, at lower pressures, viscosity is found to decrease rapidly, particularly in the regions below absolute pressures of 0.01 mm. of mercury.Viscosities calculated with the reduced state correlation produce an average over-all deviation of 0.93% for neon, argon, krypton, and xenon. In these comparisons the available viscosity data for the gaseous and liquid states of these substances have been included. Deviations of the same order of magnitude are produced for helium in the gaseous state; however, these deviations become excessive for viscosities of helium in the liquid state.The application of the final reduced state correlation has been extended to a number of diatomic and polyatomic gases and found to apply well to the diatomic gases only.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 5 (1959), S. 551-555 
    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 enthalpy of water in the liquid state has been calculated from 32°F. to temperatures approaching the critical and pressures ranging from saturated conditions to 160,000 lb./sq. in. abs. (approximately 11,000 atm). The results of this study are presented graphically and show that the influence of pressure on enthalpy is significant, particularly in the lower temperature region. At these conditions pressure is found to increase the enthalpy of liquid water by as much as 360 B.t.u./lb. above the corresponding enthalpy of the saturated liquid state.A comprehensive literature search disclosed PVT data for water that permitted the construction of a density correlation. This correlation expressed in reduced coordinates extends from the normal freezing point of water to temperatures of 1,870°F. (TR = 2.0) and pressures ranging up to 10,915 atm. (PR = 50). The recent extensive PVT data of Kennedy reported in 1950 supplemented with the earlier data of Amagat and Bridgman allowed the calculation of enthalpies at these elevated temperatures and pressures. For these calculations basic thermodynamic relationships were adapted which utilized this reduced density correlation. This approach has made possible the extension of the thermodynamic properties of liquid water above the highest pressure reported by Keenan and Keys. Below this pressure of 6,000 lb./sq. in abs. good agreement was found to exist between the enthalpy values presented by Keenan and Keyes and those reported in this investigation.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 2 (1956), S. 347-353 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: A rigorous analysis of the available data presented in the literature for all the saturated aliphatic hydrocarbons from methane through n-eicosane was conducted to establish the constants A, B, C, and D of the vapor-pressure equation developed by Frost and Kalkwarf (21). With all the constants determined, vapor pressures can be calculated accurately from the triple to the critical point. The actual constants A, B, C, and D have been calculated from the available reported vapor-pressure data of eighty-seven saturated aliphatic hydrocarbons and include all the normal paraffins through eicosane and all the isomeric paraffins through the nonanes.In order to ascertain the validity of calculated-vapor-pressure constants, values of A, B, C, and D were produced from the molecular structure and normal boiling point for all the normal paraffins through eicosane and all the thirty-four isomeric nonanes. The normal paraffins were selected to cover the range of the saturated aliphatic hydrocarbons; whereas the nonanes were chosen because they represent the most complex structures for which reported vapor pressures are available.With the calculated constants, vapor pressures were evaluated from the equation at several representative points and were compared with reported values to produce an overall absolute average percentage of deviation of 0.58 for the normal paraffins and 0.73 for the isomeric nonanes, or 0.68 for these fifty-four saturated aliphatic hydrocarbons.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 7 (1961), S. 78-80 
    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 results obtained by the evaporation of water and nitrobenzene in air from celite spheres in conjunction with the prevailing surface temperature have permitted the simultaneous determination of mass and heat transfer factors. The spheres used were 1.42, 1.88, and 2.00 in. in diameter. The experimental results of this study show that an essentially direct correspondence exists for mass and heat transfer in the flow of fluids past single spheres.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 8 (1962), S. 357-358 
    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 Frost-Kalkwarf vapor-pressure equation has been modified to include as variables the reduced temperature and pressure of the substance. The resulting relationship was found to contain a universal constant δ = 0.1832 and three other constants α, β, and γ, which are characteristic of the substance. Relationships between α, β, and γ were found to exist, and thus a vapor-pressure equation was produced which contains only one characteristic contant β and which is capable of predicting vapor pressures of pure substances up to the critical point.This vapor-pressure relationship has been applied to hydrocarbons of all types, including normal paraffins, isoparaffins, olefins, diolefins, acetylenes, naphthenes, and aromatics. In these calculations values of β were estimated from the molecular structure of the hydrocarbons. For hydrocarbons the approach developed in this study was found to reproduce experimental vapor pressures with an average deviation of 2.7% for 456 experimental points representing fifty four hydrocarbons.This study indicates that if reliable vapor-pressure data, however meager, are available for a hydrocarbon, these data can be used to obtain constants which enable the prediction of the critical temperature and the critical pressure of the substance.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 8 (1962), S. 550-553 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: The critical temperature of any multicomponent hydrocarbon system may be established solely from the normal boiling points of the pure constituents. Such mixtures may include normal paraffins, isoparaffins, olefins, acetylenes, naphthenes, and aromatics and may contain an unlimited number of components.An expression has been developed for the prediction of the critical temperatures of mixtures and has been tested on fifty-five hydrocarbon systems containing from two to five components. For 208 binary mixtures the deviations from reported values were calculated, and the maximum deviations resulting from each system were averaged for the forty-one binary systems to produce an average maximum deviation of 0.91% based on degrees absolute. For twenty-eight multicomponent mixtures reported for nine ternary, two quaternary, and three quinary systems the average deviation was 1.03%.This method presents a simple and accurate means of establishing the critical temperature of any multicomponent hydrocarbon mixture as long as the ratio of the normal boiling points of the heaviest and lightest components present in the mixture does not exceed the prescribed limits.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 8 (1962), S. 608-610 
    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: 4 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 7 (1961), S. 625-631 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Experimental viscosity, thermal conductivity, and self-diffusivity data available in the literature for carbon dioxide have been critically reviewed and used to develop reduced state correlations of the transport properties for this substance. These correlations should apply to nonpolar compounds having critical compressibility factors approximately equal to that of carbon dioxide, zc = 0.275.In order to establish the dependence of these transport properties in the high pressure and liquid state regions, use has been made of relationships between the residual properties, μ-μ*, k-k*, and (PD)*-(PD) and density. These residual quantities represent the differences between the values of the properties at any pressure and temperature and those at atmospheric pressure and the same temperature. These relationships also allow the determination of the values of the transport properties at the critical point. The resulting critical values along with the residual relationships enabled the construction of reduced state correlations for viscosity, thermal conductivity, and the product of self-diffusivity and pressure for carbon dioxide.These correlations extend from the saturated vapor and liquid states to reduced temperatures of TR = 10 and reduced pressures of PR = 50. Comparisons made between values resulting from these correlations and corresponding experimental values, including the region of high pressure for both the gaseous and liquid states and the vicinity of the critical point, produced an average deviation of 2.0% for viscosity, 1.4% for thermal conductivity, and 5.9% for self-diffusivity.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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