Sentence examples for by using a spectrometer from inspiring English sources
Raman spectra were obtained by using a spectrometer (Horiba, ARAMIS) with an Ar+ ion CW (514.5 nm) laser.
Raman spectra are recorded by using a spectrometer (Horiba, ARAMIS) with an Ar+ ion CW (514.5 nm) laser.
The 5 K PL spectra were analyzed by using a spectrometer equipped with a 600-line/mm grating and detected with a liquid-nitrogen cooled charge-coupled device (i.e., CCD detector).
The tube temperature distribution was validated by using a spectrometer system and the errors between three major product yields at the tube outlet obtained by the proposed model and in-situ measured values were within 5%.
The experimental setup was designed by using a Q-switched Nd YAG at 1064 nm with 10 Hz repetition rate, and the intensity signals from Cd II 214.441 nm, Cr II 267.716 nm and Pb II 220.353 nm emission lines were measured by using a spectrometer furnished with an intensified charge-coupled device.
A reflected shock is used to obtain pressures of ∼8.5 atm and temperatures of ∼2600 K. Visible wavelength emission spectra are recorded by using a spectrometer coupled to a streak camera, and two photodetectors record intensity vs. time at AlO emission wavelengths of 486 and 514 nm.
All samples were analyzed by using a Raman spectrometer.
Raman spectroscopy measurements were carried out by using a Raman Spectrometer (LabRAM HR Evol, HORIBA Scientific, Japan) with visible laser light (wavelength 514.5 nm) as the excitation source.
Multilayer film deposited on cotton fabrics was dried at 60°C and cured at 130°C for 3 min. XPS measurements were conducted by using a SPECS spectrometer with an Mg source and a spherical mirror analyzer working in spectrum mode.
Radiation attenuation in the infrared range and opacity in the visible range were measured, by using a FTIR spectrometer and a dedicated opacimetry device especially designed for the present application.
The analysis of beam emittance and ion species fractions from data obtained with an Allison scanner is described and the results of species fraction measurements are compared with those obtained by using a deported spectrometer.
