Sentence examples for the samples were determined using from inspiring English sources
Cell concentrations of the samples were determined using a Sysmex XE2100 haematology automated analyser.
Length and width of the samples were determined using this system.
The thermal properties of the samples were determined using differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA).
The optical band gaps and Urbach energies of the samples were determined using the dependence of the absorption coefficient on the photon energy.
Additionally, the effects of temperature and heating rate on the thermal degradation of the samples were determined using thermogravimetric analysis combined with differential thermal analysis (TGA/DTA).
The precipitate and brine samples were collected during the evaporation, and the chlorine isotopic ratios of the samples were determined using an improved thermal ionisation mass spectrometry procedure based on Cs2Cl+ ion measurement.
The anthocyanin content of the samples was determined using HPLC.
The absorbance of the samples was determined using a FilterMax F3&F5 Multi-Mode Microplate Reader (Molecular Devices).
The total content of phenolic compounds in the samples was determined using the Folin-Ciocalteu method31 with gallic acid as a calibration standard.
The bulk specific gravity of the samples was determined using the vacuum sealing method.
The zeta potential of the samples was determined using the SurPASS Instrument (Anton Paar, Graz, Austria).
