BUSCADOR RECOLECTA

Álvarez Cobelas, Miguel. Methodology of Las Madres lake study. https://doi.org/10.20350/digitalCSIC/16357 . http://hdl.handle.net/10261/360220, This dataset encompasses field data on freshwater sites sampled for environmental data and algae in Madrid County in 2019, May., Madrid Field Data (2019, May).txt, Peer reviewed

Álvarez Cobelas, Miguel. Methodology of Las Madres lake study. https://doi.org/10.20350/digitalCSIC/16357 . http://hdl.handle.net/10261/360220, This dataset encompasses nutrient data on freshwater sites sampled for environmental data and algae in Madrid County gathered in 2018-2022., Madrid Nutrient Data (2018-2022).txt, Peer reviewed

Álvarez Cobelas, Miguel. Methodology of Las Madres lake study. https://doi.org/10.20350/digitalCSIC/16357 . http://hdl.handle.net/10261/360220, This dataset encompasses nutrient data on freshwater sites sampled for environmental data and algae in Madrid County gathered in May, 2019., Madrid Nutrient Data (2019, May).txt, Peer reviewed

This dataset encompasses data on freshwater sites sampled for environmental data and algae in Madrid County in the 2017-2022 period., Madrid Sampling Sites (2017-2022).txt, Peer reviewed

[Description of methods used for collection/generation of data] IGC measurements at infinite dilution (IGC-ID) and finite dilution (IGC-FD) were carried out using a PerkinElmer Clarus 400 chromatography meter coupled with an Agilent AMD 1000 flowmeter to control the gas injections. The analysis of recorded chromatograms to obtain the isotherms was conducted using the CGI-CF V 709G software from Adscientis. For the determination of energy distribution functions, the FDRJ 07.5.F software from Adscientis was used. For the measurements at infinite dilution (IGC-ID), C3S-I, C3S-II and C3A samples were placed in a 6.4 mm (1/4 in.) measuring column, with an internal diameter of 4 mm and a length of 10 cm. Approximately 2 g of powder were placed in the columns for measurement. Due to the poor handling properties of the kaolinite and metakaolin powders, compaction, crushing and sieving was carried out beforehand. This procedure ensured a suitable gas flow rate in the IGC column. To do this, kaolinite and metakaolin samples were compacted in a pelletizing mold under a pressure of 1 ton for 2 minutes. Afterwards, the pellets were crushed and sieved. A 3.2 mm (1/8 in.) measuring column, with an internal diameter of 2 mm and a length of 10 cm, was filled with pieces with a size between 250 to 450 m. Approximately 0.35 grams of kaolinite and metakaolinite were used in each case. Before conducting the measurements, the surface of the samples inside the column was conditioned for the tests using a flow of dry helium at 5 mL/min during 16 h at 30°C. Measurements were conducted at 30°C for all samples, except kaolinite. In this case, the retention times observed were extremely long, and the measurement temperature was increased to 80°C on this sample to achieve full elution over a reasonable timeframe. Hexane, heptane, octane, nonane, isooctane, 2,2-dimethyl-hexane (2,2-DHM) and cyclooctane were used as n-alkane probes to determine the dispersive surface energy. Isooctane, 2,2-dimethyl-hexane (2,2-DMH) and cyclooctane were used as branched and cyclic probes to measure the surface nanoroughness. Acetone, acetonitrile (CH3CN), tetrahydrofuran (THF), ether, chloroform (CHCl3) and benzene were also used as polar probes to determine the acid-base character of the different cementitious materials. For IGC-FD measurements, water and isopropanol were used as probes over the set of samples with helium as carrier gas in both cases. Water was initially used over C3A and C3S-I samples. In this case, P/P0 values from 0.15 to 0.64 were explored. A strong interaction of water with the surfaces was observed, and consequently isopropanol was selected as a more suitable adsorbate to conduct further experiments. Measurements with isopropanol were done for C3A, C3S-I, C3S-II, C3S-II Ann, C3S-II-TEA, Kaolinite, MK and MK-TEA. For these measurements, the injected amount of isopropanol was fixed so to achieve a P/P0 up to 0.2, with a minimum of 3 injections. All isopropanol injections were preceded by injection pulse of methane (CH4), used as a reference to compute the retention times (TR) at each point of the chromatogram. All measurements were conducted at 30°C. For all cement phases, a 6.4 mm (1/4 in.) measuring column, with an internal diameter of 4 mm and a length of 10 cm was used. The columns were filled with 1.6-2 g of sample. In the case of C3S-II Annealed, a shorter column (3 cm, filled with 0.6 g of sample) with the same diameter was used to decrease the observed retention time. In the case of clay minerals, a 3.2 mm (1/8 in.) measuring column, with an internal diameter of 2 mm and a length of 5 cm was used, filled with 0.13 to 0.18 g of sample. The clay powders were pelletized in the same way as for the IGC-ID measurements. Isothermal calorimetry was used to characterize the reactivity of the different cement phases. Paste samples were prepared by mixing 15 g of powder with distilled water at a water-to-solids ratio of 0.35. A high shear mixer was used at 1600 rpm for 2 minutes. Afterwards, 10 grams of sample were placed in a glass ampoule and sealed. A TAM Air isothermal calorimeter was used to monitor the heat release of the samples for 7 days at 20°C. Isothermal calorimetry was also used to assess the reactivity of the different clay minerals. For this purpose, the R3 test (ASTM C1897) [16] was selected due to its reliability and ease of interpretation. In this procedure, the different clays are mixed with portlandite, calcium carbonate, potassium sulphate, potassium hydroxide and water at 40 °C, and put into glass ampoules inside the calorimeter at 40 °C. The total heat evolved is taken as a measure of the reactivity of the clays., This paper presents a preliminary study of the characterization of the surface energy properties of clinker phases (C3S and C3A), kaolin and metakaolin by Inverse Gas Chromatography (IGC). For this, a reliable measurement methodology was developed. By looking at changes in the whole series of results (dispersive surface energy, specific polar interaction parameter, acid and base constants, morphology index, nanoroughness and adsorption energy distribution function), it is possible to discern changes between the same powders with different surface treatments. A promising correlation between surface properties and the reactivity of studied materials have been found. However, based on the IGC characterization, the increased reactivity of metakaolin compared to the raw kaolinite seems to be strongly linked to the change in local order rather than significant changes in the surface energetics, although a change in the acid/base nature of the surface has been observed., Swiss Agency of Development and Cooperation (SDC) grant 81026665; Swiss National Science Foundation (SNSF) through an Ambizione fellowship (grant 208719); Consejería de Educación e Investigación (Comunidad de Madrid) which funded the 2016-T1/AMB-1434 project in the frame of “Ayudas de Atracción de Talento Investigador”; Ministry of Science and Innovation through funding PID2020-115797RB-I00/AEI/10.13039/501100011033 project., File List: DRX C3S; PSD_C3SC3A; Calculation KaKb; Data_DI&FC; Data_IGC-FC; Water_AEDF_norm; Water_AEDF, Peer reviewed

This dataset encompasses data on freshwater sites sampled for environmental data and algae in Madrid County in 2019, May., Madrid Sampling Sites (2019, May).txt, Peer reviewed

The files contain the dataset of the figures in the article "Description of ultrastrong light-matter interaction through coupled harmonic oscillator models and their connection with cavity-QED Hamiltonians", written by Unai Muniain, Javier Aizpurua, Rainer Hillenbrand, Luis Martín-Moreno and Rubén Esteban. The article will be published in the journal Nanophotonics (DOI: 10.1515/nanoph-2024-0528), MICIU/AEI/10.13039/ 501100011033 and ERDF, EU (grants PID2022-139579NB-I0 and PID2021-123949OB-I00);, MICIU/AEI/10.13039/ 501100011033 (grants Grant CEX2020-001038-M, PID2020-115221GB-C41 and CEX2023-001286-S);, Basque Government (grant IT 1526-22 for consolidated groups of the Basque University);, Department of Economy of the Basque Government (project 4usmart Elkartek);, Government of Aragon (Project Q-MAD);, Peer reviewed

Additional characterization data including NMR, FTIR, ESI HRMS, MALDI-ToF MS, DSC, rheology, and MIP results., Peer reviewed

Experimental details for the synthesis of 1, summary of crystallographic data for [1]Cl and 1 (at 173 and 296 K), comparison of the experimental and computed PXRD patterns and EPR spectra for 1 as well as additional magnetic measurements and computational studies on 1., Peer reviewed

Additional experimental details on ferroelectric poling of the PZT film; electrical characterization of the nominally neutral 180° DWs by conductive AFM; PFM images of the reorganization of the a domains after poling; STEM images illustrating the interaction between 180° and 90° DWs; details of the determination of atomic displacements around the DWs; STEM analysis of a twisted DW., Peer reviewed