Dataset for generation of figures in Air-broadening in near-infrared carbon dioxide line shapes: quantifying contributions from O2, N2, and Ar (https://doi.org/10.1016/j.jqsrt.2021.107669)

Data corresponding to Figs. 2,3,5,6,11,12,13,14 for Fleurbaey et al J. Quant Spectrosc. Radiat. Transf. vol 270, 107684 (2021). doi.org.10.1016/j.jqsrt.2021.107684

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.

These data from the laboratory tests of a prototype residential liquid-to-air ground-source air conditioner (GSAC) using CO2 as the refrigerant. The data collection and processing methods are described in detail in this report:

Report Title: "Laboratory Tests of a Prototype Carbon Dioxide Ground-Source Air Conditioner", NIST Technical Note 2068
Publication Date: October 2019
DOI: https://doi.org/10.6028/NIST.TN.2068
Authors: Harrison Skye, Wei Wu

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.

Data files for the publication "High Accuracy Near-infrared Carbon Dioxide Intensity Measurements to Support Remote Sensing" in Geophysical Research Letters

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.