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H.T. Haselton

Publications and source records attributed to H.T. Haselton.

11 recordsLinked to original sources

Techniques for determining pressure in the hydrothermal diamond- anvil cell: behavior and identification of ice polymorphs (I, III, V, VI)

For H2O densities > 1.0 g/cm3, a determination of the ice melting temperature provides the density information required to calculate the P-T path that the sample in a hydrothermal diamond-anvil cell follows when the sample is heated isochorically. The principal difficulty is the identification of the polymorph because of metastable behavior of ices in the H2O system. Usually, an accurate identification of the liquidus ice phase can be made without analytical instrumentation and requires only careful observations. -Authors

American Mineralogist

Heat capacities and entropies at 298.15 K of MgTiO3 (geikielite), ZnO (zincite), and ZnCO3 (smithsonite)

Heat capacities of synthetic MgTiO3 (geikielite), ZnO (zincite), and natural crystals of smithsonite (ZnCO3) were measured between 9 and 366 K using an automatic adiabatically shielded calorimeter. At 298.15 K the standard molar entropies Smo of MgTiO3, ZnO, and ZnCO3 are (74.64 ?? 0.15), (43.16 ?? 0.09), and (81.19 ?? 0.16) J??K-1??mol-1, respectively. Debye temperatures for MgTiO3 and ZnO calculated from our Cp, mo values below 20 K are (900 ?? 20) K and (440 ?? 25) K respectively. Heat capacities for MgTiO3 and ZnO were combined with enthalpy increments from the literature to derive heat-capacity equations for these phases from 260 to about 1800 K. The heat capacities of MgTiO3 between 260 and 1720 K were fitted with an average deviation of 0.3 per cent by the equation: C??p,m/(J??K-1??mol-1) = 222.5-0.05274(T/K)-6.092x105(T/K)-1-1874.6(T/K) -1/2+1.878x10-5(T/K)2 and for ZnO the equation: C??p,m/(J??K-1??mol-1) = 53.999+7.851x10-4(T/K)-5.868x105(T/K)-2 -127.50(T/K)-:1/2+1.9376x10-6(T/K)2 fits the heat capacities in the temperature interval of 250 to 1800 K with an average deviation of 0.7 per cent. ?? 1989.

Journal of Chemical Thermodynamics

The decarbonation and heat capacity of ZnCO3

The decarbonation curve for ZnCO 3 has been determined in the pressure range 3–20 kbar by using a combination of cold-seal vessels and piston-cylinder apparatus with NaCl assemblies. Heat capacities for both synthetic and natural ZnCO 3 samples were measured by differential scanning calorimetry at temperatures ranging from 340 to 497 K. The results of these experiments indicate that the enthalpy of formation for smithsonite, ΔH f (1,298.15), is approximately −817. kJ/mol. which is about 4 kJ more negative than most tabulated values.

Geochimica et Cosmochimica Acta

Heat capacities of synthetic hedenbergite, ferrobustamite and CaFeSi2O6 glass

Heat capacities have been measured for synthetic hedenbergite (9–647 K), ferrobustamite (5–746 K) and CaFeSi 2 O 6 glass (6–380 K) by low-temperature adiabatic and differential scanning calorimetry. The heat capacity of each of these structural forms of CaFeSiO 6 exhibits anomalous behavior at low temperatures. The X-peak in the hedenbergite heat-capacity curve at 34.5 K is due to antiferromagnetic ordering of the Fe 2+ ions. Ferrobustamite has a bump in its heat-capacity curve at temperatures less than 20 K, which could be due to weak cooperative magnetic ordering or to a Schottky anomaly. Surprisingly, a broad peak with a maximum at 68 K is present in the heat-capacity curve of the glass. If this maximum, which occurs at a higher temperature than in hedenbergite is caused by magnetic ordering, it could indicate that the range of distortions of the iron sites in the glass is quite small and that coupling between iron atoms is stronger in the glass than in the edge-shared octahedral chains of hedenbergite. The standard entropy change, S o 298.15 − S o 0 , is 174.2 ± 0.3, 180.5 ± 0.3 and 185.7 ± 0.4 J/mol·K for hedenbergite, ferrobustamite and CaFeSi 2 O 6 glass, respectively. Ferrobustamite is partially disordered in Ca-Fe distribution at high temperatures, but the dependence of the configuratonal entropy on temperature cannot be evaluated due to a lack of information. At high temperatures (298–1600 K), the heat capacity of hedenbergite may be represented by the equation C o p (J/mol·K) = 3 l 0.46 + 0.01257 T -2039.93 T −1 2 − 1.84604× l0 6 T −2 "> −12− 1.84604× 10 6 T −2 and the heat capacity of ferrobustamite may be represented by C o p (J/mol·K) = 403.83−0.04444T+ 1.597× 10 −5 T 2 −3757.3T −1 2 "> C o p (J/mol·K)= 403.83−0.04444T+ 1.597× 10 −5 T 2 −3757.3T −12 .

Geochimica et Cosmochimica Acta

Heat capacities and thermodynamic functions for beryl, Be3Al2Si6O18, phenakite, Be2SiO4, euclase, BeAlSiO4(OH), bertrandite, Be4Si2O7(OH)2, and chrysoberyl, BeAl2O4.

The heat capacities of beryl, phenakite, euclase and bertrandite have been measured between approx 5 and 800 K by combined quasi-adiabatic cryogenic calorimetry and differential scanning calorimetry. The heat capacities of chrysoberyl have been measured from 340 to 800 K. The resulting data have been combined with solution and phase-equilibrium experimental data and simultaneously adjusted using the programme PHAS20 to provide an internally consistent set of thermodynamic properties for several important beryllium phases. The experimental heat capacities and tables of derived thermodynamic properties are presented.-J.A.Z.

American Mineralogist

Akermanite: phase transitions in heat capacity and thermal expansion, and revised thermodynamic data.

A small but sharp anomaly in the heat capacity of akermanite at 357.9 K, and a discontinuity in its thermal expansion at 693 K, as determined by XRD, have been found. The enthalpy and entropy assigned to the heat-capacity anomaly, for the purpose of tabulation, are 679 J/mol and 1.9 J/(mol.K), respectively. They were determined from the difference between the measured values of the heat capacity in the T interval 320-365 K and that obtained from an equation which fits the heat-capacity and heat-content data for akermanite from 290 to 1731 K. Heat-capacity measurements are reported for the T range from 9 to 995 K. The entropy and enthalpy of formation of akermanite at 298.15 K and 1 bar are 212.5 + or - 0.4 J/(mol.K) and -3864.5 + or - 4.0 kJ/mol, respectively. Weak satellite reflections have been observed in hk0 single-crystal X-ray precession photographs and electron-diffraction patterns of this material at room T. With in situ heating by TEM, the satellite reflections decreased significantly in intensity above 358 K and disappeared at about 580 K and, on cooling, reappeared. These observations suggest that the anomalies in the thermal behaviour of akermanite are associated with local displacements of Ca ions from the mirror plane (space group P421m) and accompanying distortion of the MgSi2O7 framework.-L.C.C.

Canadian Mineralogist