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  • SPACE RADIATION  (135)
  • Chemical Engineering  (98)
  • Physics  (73)
  • STRUCTURAL MECHANICS  (72)
  • ASTROPHYSICS
  • 1970-1974  (282)
  • 1960-1964  (96)
  • 1972  (282)
  • 1963  (96)
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  • 1970-1974  (282)
  • 1960-1964  (96)
Year
  • 1
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    Manned Space Flight (1963)
    In:  Other Sources
    Details
    Publication Date: 2019-08-14
    Description: Manned space flight - summary
    Keywords: SPACE RADIATION
    Format: text
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    NASA TECHNICAL REPORTS
  • 2
    Electronic Resource
    Electronic Resource
    Dispersed phase reactor model for predicting conversion and mixing effects (1972)
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 18 (1972), S. 1268-1271 
    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: 5 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/aic.690180631
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    Paper (German National Licenses)
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  • 3
    Electronic Resource
    Electronic Resource
    Agitation of liquid systems requiring a high shear characteristic (1963)
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 9 (1963), S. 338-342 
    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: 7 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/aic.690090312
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  • 4
    Electronic Resource
    Electronic Resource
    Dispersed phase mixing: II. Measurements in organic dispersed systems (1963)
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 9 (1963), S. 196-202 
    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: When two liquid phases are contacted in a stirred tank reactor, dispersed phase mixing can affect average reaction rate and product selectivity in nonfirst order or mass transfer controlled reactions, as shown theoretically in Part I. This work is concerned with experimental measurement of the dispersed phase mixing rate. Various organic phase dispersions in water were studied in stirred tanks with a dye transfer light transmission technique. Batch experiments were performed in 0.30, 5.5, and 86-gal. vessels. The variables studied were power input per unit volume, phase fraction, impeller type, and vessel scale. Dispersed phase mixing rates were found to be in the range where they can have significant effects on chemical reactions. A typical value of the mixing rate is 10 volumes of dispersed phase/min. at a power input of 10 hp./1,000 gal. The information given here and in Part I shows for the first time the importance of these effects in reactor design.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/aic.690090212
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  • 5
    Electronic Resource
    Electronic Resource
    Effect of carbon monoxide in causing nonuniform gasification of graphite by carbon dioxide (1963)
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 9 (1963), S. 303-306 
    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: Existing theories on the effect of mass transport on the rate (uniformity) of chemical reaction within a porous solid assume that the reaction is of integer order. However the carbon-carbon-dioxide reaction has the kinetic rate form, rate = k1pCO2/(1 + k2pCO + k3pCO2). For conditions where the retarding effect of carbon monoxide is very pronounced, the buildup of small concentrations of carbon monoxide within the porous graphite can lead to appreciable nonuniformity of gasification. Thus the criteria normally used to predict uniformity of gasification break down. A numerical integration of the combined differential equation of mass transport and chemical reaction has been performed, with rate constants for the carbon-carbon dioxide reaction taken from the literature. The results indicate that extreme nonuniformity of reaction can exist even when the change in carbon dioxide concentration from the exterior of the sample to the interior is small. The results are similar to experimental determinations of non-uniformity of gasification, obtained by determining the porosity of reacted graphite samples as a function of depth from the reacting face. Experimentally nonuniformity of reaction was observed for gasification rates a hundredfold lower than the usual Thiele criteria would predict, probably because of carbon monoxide inhibition.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/aic.690090306
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  • 6
    Electronic Resource
    Electronic Resource
    Numerical solution of convective transport problems (1963)
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 9 (1963), S. 681-688 
    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: 8 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/aic.690090521
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  • 7
    Electronic Resource
    Electronic Resource
    Fracture behavior in nylon 6 fibers (1972)
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 1415-1445 
    Details
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A reaction rate model of fracture in polymer fibers is described. This model assumes that bond rupture is governed by absolute reaction rate theory with a stress-aided activation energy. It is demonstrated that the key in obtaining good agreement between the model and experiment lies in taking proper account of the variation of stress on the tie-chain molecules. The more taut chains rupture first, and the load is redistributed among the remaining unruptured tie chains. The effect of varying the temperature both in the model and in experiments on fracture in fibers is explored. Good agreement between predictions of the model and experiment is possible only with an undeterstanding of the distribution in stress on the tie chains. The distribution in stress on the chains was experimentally determined by monitoring the kinetics of bond rupture with electron paramagnetic resonance (EPR) spectroscopy. Temperature is found to have two effects on macroscopic strength. (1) The thermal energy aids the atomic stress in breaking the atomic bonds; as a consequence the rate of bond rupture of a family of bonds under a given molecular stress is increased. In this respect temperature might be viewed as decreasing the “strength” of a bond. (2) Temperature also serves to “loosen” the molecular structure and in this way modify the distribution in stress on the tie chains. To explain bond rupture and macroscopic fracture behavior quantitatively, account must be taken of both effects.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pol.1972.160100802
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  • 8
    Electronic Resource
    Electronic Resource
    EPR studies of mechanically induced bond rupture in elastomersPaper presented at the Symposium on Mechano-Chemistry of Polymers, American Chemical Society National Meeting, Washington, D. C., September 16, 1971. (1972)
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 599-606 
    Details
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Electron paramagnetic resonance (EPR) spectroscopy was used to compute the surface bond rupture density in polyurethane and to determine the phase experiencing fracture in styrene-butadiene block copolymers when these elastomers are subjected to mechanical degradation by grinding. The polyurethane grinding was done at temperatures above and below the glass transition Tg; 0.155 × 1013 radicals/cm2 of fracture surface area were formed above the Tg and 4.42 × 1013 radicals/cm2 for grinding below the Tg. These values are essentially equal to those found earlier for spherulitic polymers. In all cases the fracture appears able to progress along preferential paths so as to rupture significantly fewer molecular chains than one would expect on the basis of calculations of the number of chains passing through each square centimeter of cross section. Comparison of EPR spectra formed by grinding styrene-butadiene copolymer with those of styrene and butadiene above indicated that at cryogenic temperature, the fracture in the copolymer takes place in the butadiene phase.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pol.1972.160100403
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  • 9
    Electronic Resource
    Electronic Resource
    Chromocene catalysts for ethylene polymerization: Scope of the polymerization (1972)
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 10 (1972), S. 2621-2637 
    Details
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Chromocene deposited on silica supports of high surface area forms a highly active catalyst for polymerization of ethylene. Polymerization is believed to occur by a coordinated anionic mechanism previously outlined. The catalyst formation step liberates cyclopentadiene and leads to a new divalent chromium species containing a cyclopentadienyl ligand. The catalyst has a very high chain-transfer response to hydrogen which permits facile preparation of a full range of molecular weights. Catalyst activity increases with an increase in silica dehydration temperature, chromium content on silica, and ethylene reaction pressure. The temperature-activity profile is characterized by a maximum near 60°C, presumably caused by a deactivation mechanism involving silica hydroxyl groups. A value of 72 was estimated for the ethylene-propylene reactivity ratio (r1). Linear, highly saturated polymers are normally prepared below 100°C. By contrast with other commercial polyethylenes, the chromocene catalyst produces polyethylenes of relatively narrow molecular weight distribution. Above 100°C, unsaturated, branched polymers or oligomers are formed by a simultaneous polymerization-isomerization process.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pol.1972.150100910
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  • 10
    Electronic Resource
    Electronic Resource
    Stereochemistry of alternating isobutene-maleic anhydride, isobutene-dimethyl fumarate, and isobutene-dimethyl maleate copolymersPresented in part at the XXIIIrd International Congress of Pure and Applied Chemistry, Boston, Massachusetts, July 1971. (1972)
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 10 (1972), S. 1297-1310 
    Details
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The stereochemical composition of the free radical alternating isobutene-maleic anhydride (IB/MA), isobutene-dimethyl fumarate (IB/DMF), and isobutene-dimethyl maleate (IB/DMM) copolymers was investigated by proton magnetic resonance. In contrast to the singlet gem-dimethyl resonance found in polyisobutene or in the alternating isobutene/acrylonitrile copolymer, the gem-dimethyl resonance of IB/MA, hydrolyzed IB/MA, and esterified IB/MA is a quadruplet with peaks of approximately equal intensity. The multiplicity of the spectra is consistent with the presence of equal amounts of threo-di-isotactic and threo-di-syndiotactic triads, disproving previous claims that such copolymers are predominantly threo-di-isotactic. The spectrum of the analogous IB/DMF indicates that the copolymer is composed entirely of erythro-di- isotactic and erythro-di-syndiotactic triads. This result is consistent with the exclusive trans opening of the dimethyl fumarate double bond and provides the first example for the stereospecific double bond opening of a noncyclic monomer in free radical polymerization. In contrast, the spectrum of IB/DMM shows that the dimethyl maleate double bond opens approximately 93% cis and 7% trans during copolymerization. Since the stereochemical composition of IB/DMF and IB/DMM is not the same, it is concluded that the radicals formed from dimethyl maleate and/or dimethyl fumarate do not equilibrate freely among all the possible configurations before isobutene addition.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pol.1972.150100502
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