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Theoretical enhancement factors were compared with experimental data for the absorption using a stirred tank absorber with a plane gas-liquid interface at 25°C.
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The calculated optical absorption using a 5×5 k.p Hamiltonian, accounts well for the absorption edge.
The concentration of Dylight549 bound to the ocr dimer was calculated from absorption using a molar extinction coefficient of 150 000 M−1 cm−1 at 562 nm.
The chromatograms were monitored by UV absorption using a photodiode array detector MD-20188, JASCorp.rp., Tokyo, Japan) and by fluorescence at excitation and emission wavelengths of 460 and 520 nm, respectively, using a fluorescence detector (FP-920, JASCO Corp., Tokyo, Japan).
The diameter of each CQD was determined from the position of the absorption edge, using a previously reported empirical relationship,[ 29] and the volume calculated assuming a spherical shape.
By repeating the measurements over the absorption edge using a miscut analyser, so as to reduce the detector acceptance, it may be possible to show that the satellite intensities are indeed given by the phase shift, and so identify the origin of the twinning in LN as being through Nb, or O.
At given time intervals, the solution was analyzed by measuring the absorption spectra using a UV-Vis spectrometry.
The absorption experiments using a wetted wall contactor have been carried out over the temperature range of 298 313 K and CO2 partial pressure range of 2 14 kPa.
After processing the absorption images using a filtered back-projection or similar algorithm to reconstruct the horizontal slice, a 3D reconstruction of the whole sample image is completed (Rivers et al. 1999, 2010).
This piece of research studies the absorption process, using a viscous organic absorbent (di 2-ethylhexyl) adi 2-ethylhexylo treadipate= DEHAloaded ventogas, in treat of hydrodynamics and mass transfer.
The absorption measurement used a xenon lamp (69911, Newport) as the light source coupled with a monochromator (74125, Newport).
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