Statistical evaluation of methods for the calculation of static formation temperatures in geothermal and oil wells using an extension of the error propagation theory

The feasibility of using the more sophisticated weighted least-squares (WLS) model, as opposed to the traditional ordinary least-squares (OLS), in linear regressions of BHT data to estimate the static formation temperatures (SFT) was investigated. The most commonly used analytical methods (line-source; spherical and radial heat flow; and cylindrical heat source) were applied. Error propagation equations were derived to calculate errors in the time function of each method. These errors were combined with the BHT measurement errors to compute weighting factors for applying the WLS. Intercept uncertainties were estimated for all regressions using sets of synthetic and actual borehole logs taken from geothermal and oil applications. SFT computed with the spherical and radial heat flow method were generally greater than those from the other two methods.     

Temperature–composition–time (T–X–t) data from authigenic K-feldspar: An integrated methodology for dating fluid flow events

Integration of fluid inclusion analysis with high spatial resolution Ar–Ar dating of K-feldspar cements has been used to resolve and reconstruct palaeo-fluid flow. Fluid inclusion analysis allows discrimination of distinct cement phases, thereby identifying discrete episodes of fluid flow. Ar–Ar dating of the same cements via high spatial resolution laserprobe establishes absolute age constraints on the framework previously constructed. Integration of these two datasets yields temperature–composition–time data.     

Composition and applied sedimentology of salt from brines of the Mamfe Basin, Cameroon

Salts produced using brines of the Mamfe Basin were analysed by XRD for their mineral composition and ICP-MS for minor element composition. Halite (NaCl) and dolomite (CaMg (CO₃)₂) constitute the major minerals with minor impurities from Mo and Cd in the chlorides and Sc and Cu in the carbonates. The mineral composition is evidence of dissolution of evaporites with parent brine of marine origin. Other elements analysed are suggested to be adsorbed to these salts and result from water–rock interaction. The elements partitioned based on their correlation to other elements are suggested to derive from sulphates including barite for Ba, sulphides for Pb, Zn, silicates for Zr, Mn and oxides for V, Cr. The electrical conductance of the brines is related to the salt yield by the equation; M = 9 × 10^− 4E− 3.27, and it can be used to estimate salt yield throughout the year. Over 1200 tons of salt consisting dominantly of grade I halite are lost annually as brines across the basin. Purification is required for some minor elements including Ba, Pb, Hg and Cd for use as a condiment. A genetic relation between the parent brine, sulphide minerals and organic matter-rich sediments is proposed.     

Stable isotope evidence for the atmospheric origin of CO2 involved in carbonation of MSWI bottom ash

Stable isotopes were used to constrain the origin of CO₂ involved in the ageing process of municipal solid waste incineration (MSWI) bottom ash under open-air conditions. The δ¹³C and δ¹⁸O values of CaCO₃ occurring in MSWI bottom ash samples of variable age and the δ¹³C of the residual organic matter content were measured, and laboratory assessments made of the isotopic fractionation accompanying CaCO₃ neo-formation during accelerated carbonation experiments of bottom ash or pure lime with atmospheric or industrial CO₂. The results indicate that stable isotopic compositions exhibited by fresh and aged bottom ash samples reflect non-equilibrium processes resembling those described in the carbonation of concrete and mortar. They also lead to conclusions on the prevalent involvement of atmospheric CO₂ in the open-air carbonation of MSWI bottom ash.