Library

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of the American Chemical Society 115 (1993), S. 8427-8431 
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 92 (1990), S. 6742-6746 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The thermal behavior of hyperquenched glassy D2O was investigated by differential scanning calorimetry from 103 to 250 K, in order to investigate the isotope effect on the glass→liquid transition and on the liquid to cubic, and cubic to hexagonal ice. For a heating rate of 30 K min−1 the temperatures of the thermal effects are: 137 K for the onset of the reversible glass→liquid transition (Tg), 154 and 173 K for the beginning and the peak minimum of the crystallization exotherm, and ≈229 K for the peak minimum of the transformation cubic→hexagonal ice. Increase in heat capacity at Tg and the width of the glass transition are similar to those reported for glassy H2O. Tg of D2O is higher than that of H2O by an amount that is expected for isorelaxational and/or isoviscous states assuming that the functional form of the molecular reorientation rates with temperature is unaffected by the isotopic substitution. The increase in the temperature of crystallization of "fluid'' D2O is ≈three times greater than the increase in the glass→liquid transition which causes Tg and devitrification to become more separated in D2O than in H2O. Implications of these results for both the inferred λ-type anomally at ≈228 K in H2O and at ≈233 K in D2O, and the presumed formation of a gel-like structure at these temperatures are discussed.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 3
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: High-density amorphous ice was heated at constant pressures of between 0.52 to 1.9 GPa from 77 K up to 240 K. The formed phases were characterized by x-ray diffractograms of samples recovered under liquid N2 at 1 bar. The (meta)stability domain of ice XII thus revealed extends between (approximate)158–212 K from (approximate)0.7 to (approximate)1.5 GPa. We further discuss whether ice XII has a low-temperature region of stability within the ice VI domain. Our (meta)stability domain of ice XII is in a different region of water's phase diagram than that shown by Koza et al. [Phys. Rev. Lett. 84, 4112 (2000)]. © 2002 American Institute of Physics.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 4
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 100 (1994), S. 2743-2747 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Metastable liquid water, obtained by heating its hyperquenched glassy state above its glass→liquid transition temperature, crystallizes to cubic ice. Kinetics of this crystallization has been studied by Fourier transform infrared spectroscopy by determining the change in the spectra of stretching vibrations of the decoupled OD oscillator in 3.6 mole % HOD in H2O. The crystallization kinetics follows the equation x=[1−exp(−ktn)] and is diffusion controlled. Annealing at a temperature below its glass→liquid transition temperature alters this kinetics as the grain–growth process begins to control the early stages of crystallization.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 5
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 95 (1991), S. 6849-6855 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Amorphous solid D2O from hexagonal and cubic ices and H2O from (HF, NH3, and NH4F) doped hexagonal ice have been prepared by Whalley's method, and their thermal behavior has been investigated by differential scanning calorimetry from 103 to 250 K. For a heating rate of 30 K min−1 , the temperature of the onset of the reversible glass(large-closed-square)liquid transition, Tg, is raised by about 4 K when H2O is substituted by D2O. Doping with NH3 and NH4F causes little change in Tg but with HF Tg becomes undetectable. The increase in heat capacity at Tg is reduced by about a factor of 3 on deuteration but marginal changes occur on doping with NH3 or NH4F. The increase in Tg on deuteration is ≈4 times of that observed for the amorphous forms made from the vapor and the liquid, and more than twice of that expected from isoviscous or isorelaxational states, assuming that the functional form of the molecular reorientation rates with temperature is unaffected by isotopic substitution. NH3 and NH4F as dopants, which generally increase the reorientation rate of water molecules in hexagonal and cubic ices, have no detectable effect on the calorimetric relaxation rate of the pressure-amorphized forms, thus indicating that the increase in the concentration of Bjerrum defects for these two dopants does not alter Tg. All these observations suggest that the structure of pressure-amorphized solids is topologically different from that of the amorphous forms made from the vapor and the liquid.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 6
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 95 (1991), S. 2955-2964 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The dielectric permittivity and loss of vapor-deposited amorphous solid water (ASW) have been measured for fixed frequencies of 1 and 10 kHz from 80 K to its crystallization temperature. Similar measurements have also been made on the cubic ice formed after the crystallization of ASW and the hexagonal ice formed on heating the cubic ice. The loss tangent shows a broad sub-Tg relaxation peak centered at about 100 K and an approach towards a plateau value which appears as a shoulder. The peak is attributed to thermally activated rotation of H2O molecules with one or two dangling OH groups on the surface of the pores of the microporous sample, and the shoulder to localized motions within the network structure. Sintering of the samples on thermal cycling between 77 and ≈120 K in vacuo causes the broad peak to vanish. With increase in temperature, above Tg, the loss tangent shows the emergence of the expected α-relaxation peak of a liquid at T〉Tg, whose completion is terminated by the onset of crystallization to cubic ice at about the same temperature for 1 kHz and for 10 kHz measurements. Thereafter, crystallization becomes slower, thus allowing further observation of the low-temperature part of the α-relaxation peak.The dielectric loss of amorphous solid water at 80 K is nearly 20 times that of the cubic ice formed on its crystallization after heating to 193 K, and nearly 3.5 times higher at Tg. The dielectric loss of the cubic ice formed on crystallization tends towards a plateau value prior to rapidly increasing with increase in temperature, an evidence for a low temperature relaxation which vanishes on conversion to hexagonal ice. This relaxation indicates a remnant topologically disordered structure of intergranular water and/or stacking faults in cubic ice. Samples sintered by thermal cycling in vacuo to ≈120 K crystallized in one step, whereas those without prior thermal cycling crystallized in two steps to cubic ice. Annealing of the ASW at 130 K completely removes the broad peak at ≈100 K and reduces the magnitude of the β-relaxation process. Partial crystallization of ASW completely removes the β-relaxation process, which indicates either preferential crystallization at the local regions of high mobility in the amorphous matrix or a change in the structure of the amorphous phase during crystallization.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 7
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 91 (1987), S. 503-505 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 8
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 99 (1995), S. 5161-5165 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 9
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 98 (1994), S. 4719-4725 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 10
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 99 (1995), S. 8401-8404 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...