This dataset contains raw mechanical data (strain, stress and strain rate curvesand initial temperatures) for compression experiments performed on aluminum alloy 6061-T6using the NIST pulse-heated Kolsky Bar at strain rates between 2400 1/s and 2700 1/s and initialtemperatures from 23 °C to 527 °C and heating times ranging between 0.2 s and 3.5 s. At this time,the thermal history of the specimen during heating is not included in the dataset but this informationmay be included in a future update.

The database contains radiative line-binned opacities for lanthanides (atomic number 57<=Z<=70) and actinides (atomic number 89<=Z<=102) which are of paramount importance for simulation of light curves and spectra produced by kilonovae. The opacities were calculated by the LANL group under the assumption of local thermodynamic equilibrium. The temperature grid cover the range from 0.01 eV to 5.0 eV while the mass density grid covers 16 orders of magnitude. The database provide search and selection tools along with graphical and tabular outputs.

These four data files contain datasets from an interlaboratory comparison that characterized a polydisperse five-population bead dispersion in water. A more detailed version of this description is available in the ReadMe file (PdP-ILC_datasets_ReadMe_v1.txt), which also includes definitions of abbreviations used in the data files. Paired samples were evaluated, so the datasets are organized as pairs associated with a randomly assigned laboratory number.

Materials discovery and development necessarily begins with the preparation and identification of product phase(s). Crystalline compounds can be identified by their characteristic diffraction patterns using X-rays, neutrons, and or electrons. An estimated 20,000 X-ray diffractometers and a comparable number of electron microscopes are used daily in materials research and development laboratories for this purpose.

This is a file containing aggregation data for two proteins that were thermomechanically aggregated. The aggregated proteins were separated by asymmetric flow field flow fractionation and separated protein fractions were detected and quantified by UV spectrophotometry and multi-angle light scattering. The UV spectrophotometry was used to quantify the amount of residual monomer, which is reported herein. The multi-angle light scattering was fitted to a relevant model to calculate the molecular weight of the aggregated protein, also reported herein.

This Standard Reference Material (SRM) is intended for use as a primary calibration standard for the quantitative determination of barium. A unit of SRM 3104a consists of five 10 mL sealed borosilicate glass ampoules of an acidified aqueous solution prepared gravimetrically to contain a known mass fraction of barium. The solution contains nitric acid at a volume fraction of approximately 1 %, which is equivalent to a concentration (molarity) of approximately 0.16 mol/L. This data is public in the Certificate of Analysis for this material.

This Standard Reference Material (SRM) is intended for use as a primary calibration standard for the quantitative determination of cerium. A unit of SRM 3110 consists of five 10 mL sealed borosilicate glass ampoules of an acidified aqueous solution prepared gravimetrically to contain a known mass fraction of cerium. The solution contains nitric acid at a mass fraction of approximately 16 %. This data is public in the Certificate of Analysis for this material.

This Standard Reference Material (SRM) is intended for use as a primary calibration standard for the quantitative determination of germanium. A unit of SRM 3120a consists of 50 mL of a single element solution in a high density polyethylene bottle sealed in an aluminized bag. The solution was prepared gravimetrically to contain a known mass fraction of germanium. The solution contains nitric acid at a concentration of approximately 1.6 mol/L and hydrofluoric acid at a concentration of approximately 0.6 mol/L. This data is public in the Certificate of Analysis for this material.

This Standard Reference Material (SRM) is intended for use as a primary calibration standard for the quantitative determination of hafnium. A unit of SRM 3122 consists of 50 mL of an acidified aqueous solution prepared gravimetrically to contain a known mass fraction of hafnium in a high density polyethylene bottle sealed in an aluminized bag. The solution contains approximately 8 % nitric acid (volume fraction) and approximately 1 % hydrofluoric acid (volume fraction), equivalent to amount of substance concentrations (molarities) of 1.3 mol/L and 0.3 mol/L, respectively.

This Standard Reference Material (SRM) is intended for use as a primary calibration standard for the quantitative determination of lanthanum. A unit of SRM 3127a consists of five 10 mL sealed borosilicate glass ampoules of an acidified aqueous solution prepared gravimetrically to contain a known mass fraction of lanthanum. The solution contains nitric acid at a volume fraction of approximately 10 %, equivalent to an amount of substance concentration (molarity) of approximately 1.6 mol/L. This data is public in the Certificate of Analysis for this material.