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The data set encompasses the data generated through the 8 experimental runs on the 25 kWth calcium looping pilot plant at Cranfield University arranged into 8 functional Excel spreadsheets. The operational data are gathered by the acquisition with Labview software (the composition of the gas from the calciner and carbonator; temperatures of the electrical furnaces on the preheating lines and around the calciner; temperatures of the gas in the preheating lines and in the calciner) and Pico software (temperatures in the carbonator and lower loop seal and pressures in the calciner and in the carbonator). Moreover, the data from the experimental diary (inputs of gasses and solids into the rig) and the data from the post-processing of the extracted solids are included. All the data are combined into comprehensible charts that describe and explain the experimental runs together with the mass and energetic model of the system during steady state operations.
We used existing coretop samples from several sites from the Atlantic, Arctic, Pacific, and Indian Oceans (Fig. 1 and Table S1) to test the relationship between Mg/Ca ratios and D47 values in modern foraminifera. In the North Atlantic the cores were the same as those used previously by Elderfield and Ganssen (2000) (Tables S1 and S2). Coretops with the potential to yield large (>5 mg) mono-specific samples of foraminifera were selected from the >300 lm size fraction of the sediment except for Neogloboquadrina pachyderma (sinistral) where the >150 lm size fraction was chosen to obtain sufficient material. After cleaning the samples consisted of _3 mg of foraminiferal calcite and included 8 different species of surface- and deepdwelling planktonic foraminifera: Globigerina bulloides, Globigerinoides sacculifer, Globorotalia hirsuta, Globorotalia inflata, Globorotalia menardii, Neogloboquadrina dutertrei, Neogloboquadrina pachyderma (s), and Orbulina universa. The Godwin Laboratory clumped isotope calibration (i.e., the regression between D47 and temperature) was established using natural cave carbonates that precipitated subaqueously at known temperatures, ranging from 3 to 47ºC (Table 1, Fig. 2). These carbonates grew under conditions that minimize CO2-degassing and evaporation and hence kinetic fractionation effects are negligible owing to an unlimited DIC pool in the water (Kele et al., 2015). All samples consist of calcite, except NAICA-1 which is aragonite.
This dataset represents the first publication of complete national maps from the Geochemical Baseline Survey of the Environment (G-BASE) and TellusNI projects, whose aim was to conduct a national geochemical survey of the United Kingdom in order to improve understanding of our geology and environment and provide quantitative evidence against which to gauge future environmental change. This dataset consists of a series of interpolated raster (ASCII grid) maps displaying the concentrations of a suite of chemical elements (and oxides) in the stream sediments of the United Kingdom. The chemical elements are as follows: Arsenic, Barium, Calcium (CaO), Chromium, Cobalt, Copper, Iron (Fe2O3), Lanthanum, Lead, Magnesium (MgO), Manganese (MnO), Nickel, Potassium (K2O), Rubidium, Uranium, Vanadium, Zinc and Zirconium.
The London Earth data is part of a nationwide project to determine the distribution of chemical elements in the surface environment, namely Geochemical Baseline Survey of the Environment (G-BASE). London Earth focuses on the soil of the capital city, the limits of the survey being defined by the Greater London Authority (GLA) administrative boundary. Chemical elements have been determined by X-ray fluorescence spectrometry (XRFS) at the laboratories of the British Geological Survey (BGS) in Keyworth, Nottingham. These results are presented as a MS Excel file.