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Bruch S. Hemingway

Publications and source records attributed to Bruch S. Hemingway.

18 recordsLinked to original sources
USGS2002

Thermodynamic data for modeling acid mine drainage problems: compilation and estimation of data for selected soluble iron-sulfate minerals

Enthalpy of formation, Gibbs energy of formation, and entropy values have been compiled from the literature for the hydrated ferrous sulfate minerals melanterite, rozenite, and szomolnokite, and a variety of other hydrated sulfate compounds. On the basis of this compilation, it appears that there is no evidence for an excess enthalpy of mixing for sulfate-H2O systems, except for the first H2O molecule of crystallization. The enthalpy and Gibbs energy of formation of each H2O molecule of crystallization, except the first, in the iron(II) sulfate - H2O system is -295.15 and -238.0 kJ?mol-1, respectively. The absence of an excess enthalpy of mixing is used as the basis for estimating thermodynamic values for a variety of ferrous, ferric, and mixed-valence sulfate salts of relevance to acid-mine drainage systems.

Open-File Report↗
USGS1995

Estimating heat capacity and heat content of rocks

New heat-capacity measurements are reported for four rock types; Westerly granite from Bradford, RI, andesite from Lake County, OR, peridotite from Sonoma County, CA, and basalt from the Columbia River Group. Measurements were made on powders of the rocks in the temperature range of 340 to about 1000 K. Our measured heat-capacity values for rocks and other measurements of heat capacity or heat content of rocks found in the literature have been compared with estimated rock heat capacities calculated from the summation of heat capacities of both minerals and oxide components. The validity of calculating the heat content or heat capacity of rocks to better than about ± 3% from its mineral or chemical composition is well demonstrated by the data presented here.

Open-File Report↗
USGS1982

Heat capacities and entropies of Mg2SiOa, Mn2SiOa, and Co2SiOa between 5 and 380 K

The heat capacities of synthetic single crystats of Mg2Sio4 (forsterite), Mn2Sioa (tephroite), and co2Sioa (cobalt olivine), were measured between 5 and 3g0 K using an adiabatically shieldedc alorimeter. Mg2SiOais diamagnetic,a nd its heat capacity follows a normal sigmoidal curve at low temperatures. co2sioa shows a single sharp )r-type transition at 49.85+0102 K associated with the antiferromagnetic ordering of the magnetic moments of the Co2+ ions into a collinear spin arrangement below 49.8 K. In contrast to co2sioa, Mn2Sioah ast wo transitionsi n ci, a sharpL -typet ransitiona t 47.3g10.05K and a smaller "shoulder" in Ci centered near 12 K. The upper transition corresponds to the paramagnetic (disordered) to collinear antiferromagnetic ordering of the Mn2+ moments, whereas the shoulder near 12 K corresponds to the change from the collinear to a canted spin structure. Our calorimetric values for the antiferromagnetic-paramagnetictr ansition temperature (N6el Temperature) are in excellent agreement with those obtained by powder magnetic susceptibility measurements, 49t2 K and 5015 K for co2Sioa and Mn2Sioa respectively. The thermal Debye temperature, 0$, of Mg2Sioa calculated from our c$ measurements between 6.3 and 13.8 K is 768+15 K and agrees well with the elastic vaiue ofi of 758 K based on the mean sound velocity calculated from the room temperature elastic stiffness constants (ci:) of Graham and Barsch. At 298.15K (25"c) the molar heat capacitiesa re 118.6,1 28.7, and 133.4J /(mol . K) and the molar entropiesa re 94.11-r0.101, 55.910.4a nd,1 42.6-+0.J2l (mol . K) respectivelyf or Mg2SiO4M, n2SiOaa, nd Co2SiOa.

American Mineralogist↗
USGS1981

Thermodynamic tabulations for selected phases in the system CaO-Al 2 O 3 -SiO 2 -H 2 at 101.325 kPa (1 atm) between 273.15 and 1800 K

The standard thermodynamic properties of phases in the lime‐alumina‐silica‐ water system between 273.15 and 1800 K at 101.325 kPa (1 atm) were evalated from published experimental data. Phases included in the compilation are boehmite, diaspore, gibbsite, kaolinite, dickite, halloysite, andalusite, kyanite, sillimanite, Ca‐Al cliniopyroxene, anorthite, gehlenite, grossular, prehnite, zoisite, margarite, wollastonite, cyclowollastonite ( = pseudowollastonite), larnite, Ca olivine, hatrurite, and rankinite. The properties include heat capacity, entropy, relative enthalpy, and the Gibbs energy function of the phases and the enthalpies, Gibbs energies, and equilibrium constants for formation both from the elements and the oxides. Tabulated values are given at 50 K intervals with the 2‐sigma confidence limit at 250 K intervals. Summaries for each phase give the temperature‐ dependent functions for heat capacity, entropy, and relative enthalpy and the experimental data used in the final evaluation.

Journal of Physical and Chemical Reference Data↗