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A high-pressure steel tubing connected the sample vessel to the gas meter.
The impurity enrichment factors for such sampling devices are functions of the sampler size, and the sample vessel pressures before and after enrichment.
Also, the image could not be segmented employing the proposed segmentation method without preprocessing as depicted in Figure 16g.Another sample vessel segmentation result for a non-pathological fundus image from STARE dataset is depicted in Figure 17.
The non-uniform intensities in the given image are estimated and corrected properly.A sample vessel segmentation result for a non-pathological fundus image from our dataset is shown in Figure 16.
The step velocity of the tetragonal hen egg-white lysozyme (1 1 0) crystal plane toward the [0 0 1] direction could be controlled and measured accurately on a nanometer scale using a specially designed sealed sample vessel on an atomic force microscope.
Then 10 mL of HNO3 was added to the sample vessel.
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The sample vessels were end-over-end shaken overnight at room temperature.
Stainless steel sample vessels were filled with 0.76 g of the sample solution and the water-filled reference vessel matched to this within 1 mg.
Samples were separated during milking into sample vessels (capacity about 1 liter) controlled by milk flow rate and total amount of milk (Metatron P21, GEA WestfaliaSurge, Boenen, Germany).
Each respondent was asked to extract water from the storage container as s/he normally would and to pour it into the sampling vessel.
The Salivette sampling device with no preservative (Sarstedt) was used, the tube consisting of a plastic sampling vessel with a sterile neutral cotton wool swab, which had to be chewed for about 30 s and then returned to the insert.
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