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The sample is detected for 36 min.
Here, the absorption of the sample is detected as a function of time after the laser flash for the two wavelength regions (blue curve: 490 550 nm; red curve: 550 630 nm).
Scattered light from the sample is detected by a photomultiplier tube (PMT) (R6357, HAMAMATSU Photonics K. K., Japan) located below the cuvette.
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A second, highly mobile, amorphous phase, making up (0.8±0.2)% of the sample, was detected by 1H NMR.
The radiation transmitted through the sample was detected using a Ge Ga impurity photodetector.
(PL) spectrum of the sample was detected on a Hitachi H-4500 fluorespectrometerrometer using a Xe lamp as the light source.
To remove endotoxin, the protein sample was applied to polymyxin B column (Bio-Rad, CA, USA), and the lipopolysaccharides (LPS) content of the sample was detected using chromogenic limulus amoebocyte lysate assay (Associates of Cape Cod, MA, USA).
Afterwards, the mixture was filtered and washed by deionized water for several times until no acid on the sample was detected or up to pH 6. Opened MWNTs were dried at 90 °C for overnight.
Complete degradation of phenol was recorded at a dosage of 0.5 g/L in 45 min while at Fe+2 dosage of 0.8 g/L, a yellow color of the sample was detected which indicates excess of iron dosage.
Quantification of the EPR signal in Fig. 2C revealed that only 8.89% of the iron in the sample was detected in the EPR experiments.
Secondary electrons emitted from the sample were detected and the image was formed.
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CEO of Professional Science Editing for Scientists @ prosciediting.com