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  • 1975-1979  (18)
  • 1930-1934
  • Chemistry  (14)
  • Engineering  (2)
  • Photosynthesis  (2)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Pure and applied geophysics 117 (1978), S. 498-512 
    ISSN: 1420-9136
    Keywords: History of atmosphere ; Oxygen ; Ozone ; Photosynthesis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences , Physics
    Notes: Abstract There may have been three stages in the growth of oxygen in the terrestrial atmosphere. Prior to the origin of photosynthesis the only source of oxygen was photolysis of water vapor followed by escape of hydrogen to space. The rate of this process was probably less than the rate of release of reduced gases (principally hydrogen) from volcanoes, so the oxygen partial pressure was held to negligibly low values by photochemical reactions with an excess of hydrogen. The photosynthetic source of oxygen was probably in operation as long ago as 3.8 billion years. It released oxygen to the ocean. Presumably most of this oxygen was destroyed in the ocean as long as its rate of supply was less than the rate of supply of readily oxidizable material (principally Fe2+) provided by the weathering of rocks. This phase appears to have lasted until about 2 billion years ago, during which period most banded iron formations were deposited. During this period the production of oxygen by algae was limited by competition with photosynthetic bacteria, which preempted the supply of nutrient phosphorus as long as reduced chemicals were available in the environment. Once the photosynthetic oxygen source exceeded the rate of supply of reduced minerals exposed by erosion and weathering, the accumulation of oxygen in the ocean and atmosphere could be controlled only by reaction of oxygen with reduced organic material. This is the stabilization mechanism that operates today. It seems unlikely that oxygen could be consumed at a significant rate by this process until oxygen levels sufficiently high to support respiration had been achieved. I therefore suggest that atmospheric oxygen rose rapidly from essentially zero to approximately its present value (within a factor of 10) when the photosynthetic source of oxygen rose above the weathering source of reduced minerals, probably about 2 billion years ago. The ozone layer and the ultraviolet screen were absent prior to this time and essentially fully developed after this time.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Pure and applied geophysics 116 (1978), S. 222-231 
    ISSN: 1420-9136
    Keywords: Photolysis ; Photosynthesis ; Primitive Atmosphere
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences , Physics
    Notes: Abstract From time to time there appears in the literature the assertion that photolysis of water vapor could have maintained an appreciable concentration of oxygen in the primitive (prebiological) atmosphere. The implausibility of this assertion is argued in this paper. By itself, photolysis does not provide a source of oxygen because it is usually followed by recombination of the products of photolysis. Only the escape to space (at a much smaller rate) of the hydrogen produced by photolysis of water results in a net source of oxygen. The oxidation state of the primitive atmosphere depended on the relative magnitudes of this net source of oxygen and a volcanic source of hydrogen and other reduced gases. Today the volcanic source of reduced gases is approximately equal to the oxygen source provided by photolysis followed by escape. The oxygen source depends on the mixing ratio of water vapor in the stratosphere, which ultimately determines the rate of escape of hydrogen produced from water vapor. Its magnitude may not have been very different in the past. The volcanic source of hydrogen, on the other hand, is likely to have been much larger when the earth was tectonically young. Hydrogen was therefore released to the primitive atmosphere more rapidly than oxygen, probably. Photochemical reactions with the excess hydrogen maintained oxygen mixing ratios at negligibly small levels. The hydrogen mixing ratio was determined by a balance between the volcanic source (reduced by recombination with oxygen) and escape to space. In time, either because of decline of the volcanic source of hydrogen or because of addition of a biological source of oxygen, the input of oxygen to the atmosphere rose above the input of hydrogen. The oxidation state of the atmosphere changed rapidly. Volcanic hydrogen was now consumed by photochemical reactions with excess oxygen, while the oxygen mixing ratio was determined by a balance between the source (reduced by recombination with volcanic hydrogen) and consumption in reactions with reduced material at the surface.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    International Journal for Numerical Methods in Engineering 11 (1977), S. 1405-1421 
    ISSN: 0029-5981
    Keywords: Engineering ; Engineering General
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Mathematics , Technology
    Notes: In this paper we describe a new class of locally refined macro finite elements which are especially amenable to the use of substructuring techniques for the efficient solution of the resulting idealization. The tools and guidelines illustrated by the examples of modelling crack tips, point load singularities and singularities at re-entrant corners should enable an analyst to construct other such blended macro elements specifically tailored to his particular class of problems. The use of such substructured macro elements in finite element calculations permits substantial reduction in the manual effort of data preparation and the computational cost of numerical solution.
    Additional Material: 18 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    International Journal for Numerical Methods in Engineering 12 (1978), S. 1841-1851 
    ISSN: 0029-5981
    Keywords: Engineering ; Engineering General
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Mathematics , Technology
    Notes: A common method for numerically approximating two-point parabolic boundary value problems of the form ut = L[u]+f(u) defined of the semi-infinite strip S = [0, 1]×[0, ∞] is to first discretize the spatial operator in the differential equation and then solve for the time evolution. Such an approach typically involves solving a system of algebriaic equations at a sequence of time steps. In this paper we take a different approach and subdivide S into a collection of semi-infinite substrips Si = [xi, xi+1]×[0, ∞], and use blending function techniques to derive finite parameter functions ei(x, t) defined on Si. Spectral matching methods are used in deriving ei to ensure that (u - ei) can be made small on Si. Galerkin's method, with associated integration sover the entire space-time domain S, is then used to generate approximations to u(x, t) based upon the so defined infinite element (ei, Si). Approximations are hence found for all (x, t) in S by solving one well structed system of algebraic equations. We apply the method to several linear and non-linear problms.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Biotechnology and Bioengineering 18 (1976), S. 179-187 
    ISSN: 0006-3592
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: The glucose oxidase and catalase activities immobilized to the γ-aminopropyltriethoxysilane derivative of nickel-impregnated silica alumina was controlled by several factors. The most important of these was enzyme concentration. In constructing the dual immobilized enzyme catalyst, competition between the two enzymes for available binding sites was observed. The order of addition of the various reactants during immobilization was also important. Higher glucose oxidase activities were immobilized when glutaraldehyde was added concurrently with the enzyme, while maximal coupling of catalase occurred if glutaraldehyde was first added to react with the amino derivative of the silica alumina support, excess reagent washed away, and then the catalase added. Bovine serum albumin, which aids in the crosslinking of glucose oxidase, hindered the coupling of the enzyme to the support particles.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 24 (1978), S. 1000-1010 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Correlations producing thermodynamic property tables employ the concepts of scaling with increasing frequency in the vapor-liquid critical region. One of the important concepts is that the vapor pressure equation should provide infinite curvature and finite slope ψc at the critical point. The vapor pressure critical exponent θ describes the divergent curvature in a power law expression.This paper provides an extensive study of θ. We have determined an optimal value of θ by two general approaches: a curve fit method (CFM) which employs least-squares analyses, and a numerical derivative method (NDM). The CFM is interpolative but requires a vapor pressure equation, while the NDM is extrapolative but is independent of the vapor pressure equation.The vapor pressure equations, which satisfy scaling concepts most closely, exhibit a very flat minima for the CFM. As a result, the values of θ which provide reasonable correlations vary over an appreciable range (depending upon the compound, form of the equation, and the temperature range). The NDM did not present any particular difficulties. Our overall weighted average for θ is 0.199 with a standard deviation of 0.052, while the overall numerical average was 0.225 with a standard deviation of 0.045; the final recommended value of θ is 0.22 ± 0.04.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 90 (1978), S. 546-547 
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 54 (1976), S. 49-54 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die Massenspektroskopie gilt gewöhnlich nicht als geeignete Methode zur Untersuchung von Polymeren, weil Polymere sich vor dem Verdampfen zersetzen. Wenn jedoch niedermolekulare Oligomere im Polymeren enthalten sind, oder wenn sie sich unter den im Massenspektrometer gegebenen Bedingungen bilden, dann kann die Massenspektrometrie zur Charakterisierung dieser Oligomeren herangezogen werden.Wenn Polyäthylenterephthalat (PET) in der Ionenquelle des Massenspektrometers erhitzt wird, werden cyclische Oligomere vom Dimeren bis zum Hexameren gefunden. Da das vorherrschende extrahierbare Oligomere in PET das cyclische Trimere ist, wurde eine gründliche Untersuchung seines Massenspektrums durchgeführt, um den Mechanismus der Fragmentierung zu ermitteln. Die Informationen aus dieser Untersuchung dienten zur Identifizierung der anderen cyclischen Oligomeren. Es wurde versucht, den Bildungsmechanismus der cyclischen Oligomeren durch Vergleich der Spektren von extrahiertem PET und PET mit benzoatverkappten Endgruppen herauszufinden, aber aus den Ergebnissen konnten wegen der unvollständigen Umsetzung der Hydroxylendgruppen keine Schlusse gezogen werden.
    Notes: Mass spectrometry is not usually considered a satisfactory tool for examining polymers, since polymers usually decompose before vaporizing. However, if low molecular weight oligomers are present in the polymer or if they are formed under the conditions prevailing in the mass spectrometer, then mass spectrometry might be used to characterize these low molecular weight oligomers.When poly(ethylene terephthalate) (PET) is heated in the source of a mass spectrometer, cyclic oligomers from the dimer through the hexamer are observed. Since the predominant solvent extractable oligomer present in PET is the cyclic trimer, a thorough investigation was made of its mass spectrum to determine the mechanism of ion fragmentation. The information from this investigation was used to identify the other cyclic oligomers produced. An attempt was made to determine the mechanism of formation of the cyclic oligomers by comparing spectra of extracted PET and PET with benzoate capped end groups, but the results were inconclusive because of the improbability of removing all hydroxyl ends.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 19 (1979), S. 953-954 
    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
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 19 (1979), S. 975-994 
    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 modules and birefringence of oriented polymers are known to couple through the structural and intrinsic properties of the polymer. Recent developments in both optical and mechanical theories have allowed this coupling to be expanded so that it includes predictions of modulus and refractive indices of uniaxially-oriented polymer films at various angles to the draw direction. The validity of these theories has been tested in this study by predicting the angular dependence of the optical and mechanical properties of seven uniaxiallyoriented films of isotactic polypropylene. The present study also provides intrinsic material properties associated with the crystalline and noncrystalline components of the polymer, and consequently allows the identification of the structural parameters that control the properties of ultra-high oriented isotactic polypropylene.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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