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  • 1
    Online Resource
    Online Resource
    American Chemical Society (ACS) ; 1964
    In:  The Journal of Physical Chemistry Vol. 68, No. 6 ( 1964-06), p. 1566-1567
    In: The Journal of Physical Chemistry, American Chemical Society (ACS), Vol. 68, No. 6 ( 1964-06), p. 1566-1567
    Type of Medium: Online Resource
    ISSN: 0022-3654 , 1541-5740
    RVK:
    Language: English
    Publisher: American Chemical Society (ACS)
    Publication Date: 1964
    detail.hit.zdb_id: 2006064-6
    detail.hit.zdb_id: 3003-X
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  • 2
    Online Resource
    Online Resource
    AIP Publishing ; 1963
    In:  The Journal of Chemical Physics Vol. 38, No. 11 ( 1963-06-01), p. 2725-2735
    In: The Journal of Chemical Physics, AIP Publishing, Vol. 38, No. 11 ( 1963-06-01), p. 2725-2735
    Abstract: The unilateral flow of saturated mercury vapor through cylindrical channels of stainless steel and a thin-edged orifice into a vacuum has been investigated at source pressures ranging from 10—6 to 1 atm. The results generally agree with the semitheoretical equation derived by Knudsen in a study of the bilateral flow of permanent gases under small pressure gradients, but significant differences exist. For channels with ratios of length to radius of about 60 to 100 and radii of about 0.02 cm, the agreement is within the experimental errors for pressures ranging from the lowest of 10—6 to about 5×10—4 atm. Above this latter value the rate of flow is less than that predicted by the equation, and at pressures near 1 atm the rate tends to approach that value which is expected for a situation in which the channel is filled with the saturated vapor. For the thin-edged orifice the results display the molecular flow and a transition to hydrodynamic flow which is nearly isothermal. For an intermediate value of the ratio (∼5) the results at the lowest pressures are about 6% less than those predicted by molecular flow and show a transition to a flow which tends to approach isothermal hydrodynamic flow and which is greater than molecular flow divided by the transmission probability.
    Type of Medium: Online Resource
    ISSN: 0021-9606 , 1089-7690
    Language: English
    Publisher: AIP Publishing
    Publication Date: 1963
    detail.hit.zdb_id: 3113-6
    detail.hit.zdb_id: 1473050-9
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  • 3
    Online Resource
    Online Resource
    AIP Publishing ; 1964
    In:  The Journal of Chemical Physics Vol. 41, No. 4 ( 1964-08-15), p. 1051-1062
    In: The Journal of Chemical Physics, AIP Publishing, Vol. 41, No. 4 ( 1964-08-15), p. 1051-1062
    Abstract: Approximate wavefunctions for the low-lying 1Σ+ state of the titanium monoxide molecule have been calculated by the method of Roothaan at three internuclear distances about the minimum of the potential energy curve. Basis orbitals were chosen to represent the principal effects of distortion and polarization of the atomic constituents for a very limited set of atomic basis orbitals. The calculations yield approximate Hartree—Fock molecular constants and binding energies for the 1Σ+ state, and for the 3Δ ground state and other excited states relative to the 1Σ+ state. An empirical estimate of the net molecular correlation energy relative to separated atoms is made using purely atomic data for appropriate ionic constituents of the molecule. The computed dissociation energies are in qualitative agreement with experimental values but have small errors partly owing to the approximations employed in the calculations. The ground-state parameters obtained here are De=5.61 eV, Re=1.539 Å, ωe=1263 cm—1, compared with experimental values De=6.86±0.30 eV, Re=1.620 Å, ωe=1008.4 cm—1.
    Type of Medium: Online Resource
    ISSN: 0021-9606 , 1089-7690
    Language: English
    Publisher: AIP Publishing
    Publication Date: 1964
    detail.hit.zdb_id: 3113-6
    detail.hit.zdb_id: 1473050-9
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  • 4
    Online Resource
    Online Resource
    AIP Publishing ; 1963
    In:  The Journal of Chemical Physics Vol. 38, No. 9 ( 1963-05-01), p. 2064-2074
    In: The Journal of Chemical Physics, AIP Publishing, Vol. 38, No. 9 ( 1963-05-01), p. 2064-2074
    Abstract: Previously presented analyses of the molecular flow of saturated vapor from a condensed phase in an isothermal enclosure have introduced simplifying approximations early in the treatments. Consequently functions and subtle inconsistencies have appeared which can be recognized, identified, and understood only by returning to the original formulation. A more desirable procedure is to pursue rigorously as far as possible the problem before introducing approximations. The presently described analysis differs from the others in the following respects: (1) The precise system described and the fundamental assumptions employed are defined initially. (2) For a cylindrical (and a generalized) enclosure it is shown that the form p=pe(1—Δ) with pe equal to the equilibrium pressure and Δ a function of the parameters of the cell is a convenient one for the purpose of effecting approximations. (3) The exact physical system corresponding to the classical equation, pe=p[1+(S0/S1)] , in which S0 is the area of an orifice and S1 is the evaporating area (both on a spherical surface), has been found to be a spherical enclosure for which Δ can be easily calculated. (4) The single approximation leading to the formulation of Whitman and of Motzfeldt has been found and Δ has been evaluated. An intercomparison is given.
    Type of Medium: Online Resource
    ISSN: 0021-9606 , 1089-7690
    Language: English
    Publisher: AIP Publishing
    Publication Date: 1963
    detail.hit.zdb_id: 3113-6
    detail.hit.zdb_id: 1473050-9
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  • 5
    Online Resource
    Online Resource
    American Chemical Society (ACS) ; 1963
    In:  The Journal of Physical Chemistry Vol. 67, No. 12 ( 1963-12), p. 2644-2647
    In: The Journal of Physical Chemistry, American Chemical Society (ACS), Vol. 67, No. 12 ( 1963-12), p. 2644-2647
    Type of Medium: Online Resource
    ISSN: 0022-3654 , 1541-5740
    RVK:
    Language: English
    Publisher: American Chemical Society (ACS)
    Publication Date: 1963
    detail.hit.zdb_id: 2006064-6
    detail.hit.zdb_id: 3003-X
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  • 6
    Online Resource
    Online Resource
    Rockefeller University Press ; 1963
    In:  The Journal of General Physiology Vol. 46, No. 5 ( 1963-05-01), p. 851-882
    In: The Journal of General Physiology, Rockefeller University Press, Vol. 46, No. 5 ( 1963-05-01), p. 851-882
    Abstract: Using frog's sartorius muscles we have found no correlation between phosphocreatine hydrolysis and shortening under conditions (iodoacetate poisoning and anoxia) where this reaction was the only expected source of energy. Phosphocreatine hydrolysis did, however, show a constant term corresponding to the activation heat of A.V. Hill, and a linear term with work. It was concluded that shortening heat comes from some other chemical reaction, or else Hill's equation (E = A + W + ax) fails to describe correctly the energy output in a complete cycle of contraction and relaxation. To decide between these possibilities direct measurements of heat and work during a complete cycle were made. Also, experiments were performed in which heat, work, and phosphocreatine breakdown were measured simultaneously on the same muscles. The total energy output in a complete twitch could be most simply represented by a fixed "activation" heat, plus the work. There was no term corresponding to the shortening heat. Hill's equation must, therefore, be held as invalid for the complete isotonic twitch. A value of 9.8 ± 0.5 (sE) kcal/mole was obtained for the in vivo heat of hydrolysis of phosphocreatine. This quantity showed no significant dependence on load, and it is in good agreement with the value obtained from thermochemical data. It is concluded that phosphocreatine hydrolysis and its associated buffer reactions can account quantitatively for the total energy output of isometric and isotonic twitches.
    Type of Medium: Online Resource
    ISSN: 1540-7748 , 0022-1295
    Language: English
    Publisher: Rockefeller University Press
    Publication Date: 1963
    detail.hit.zdb_id: 1477246-2
    SSG: 12
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  • 7
    Online Resource
    Online Resource
    AIP Publishing ; 1964
    In:  The Journal of Chemical Physics Vol. 40, No. 2 ( 1964-01-15), p. 613-614
    In: The Journal of Chemical Physics, AIP Publishing, Vol. 40, No. 2 ( 1964-01-15), p. 613-614
    Type of Medium: Online Resource
    ISSN: 0021-9606 , 1089-7690
    Language: English
    Publisher: AIP Publishing
    Publication Date: 1964
    detail.hit.zdb_id: 3113-6
    detail.hit.zdb_id: 1473050-9
    Location Call Number Limitation Availability
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