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Rat livers were weighed in a clean beaker.
The rats' livers were then removed and transferred to clean beaker and weighed.
After the black solution cooling down to room temperature naturally, 50 μL of OA, 50 μL of OAm, and absolute ethanol were added into the mixture to a total volume of 80 mL in a clean beaker.
The above-prepared UiO-66 powders (0.2 g) were placed into a clean beaker, which contained 200 mL of deionized water and mixed with appropriate amount of H2PdCl4 solution, and were vigorously stirred for another 1 h to disperse them completely.
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Room temperature and hot water bath samples were placed in clean beakers with 100 and 250 ml milliQ water (i.e., 18 megaohms), respectively.
For measuring pH, 100 ml of the sample taken in a clean dry beaker stirred well until reached the stable value.
The plant water extracts were digested with 5 mL of concentrated HNO3 (Suprapure, Merck) and 2 mL of H2O2 (Suprapure, Merck) in a clean glass beaker and heated on a hot plate and diluted to 10 mL with double deionized water (Milli-Q Millipore 18.2 MW/cm resistivity).
The solutions of PVP and AgNO3 were prepared separately by dissolving appropriate amounts of AgNO3 (10 and 25 mM AgNO3 in 10 ml) and PVP in distilled water and in well-cleaned dry beakers at room temperature.
Even when the membrane cleaned in the beaker was also physically cleaned (wiping the surface) the recovered flux was still 20% less than that obtained for membranes cleaned in place.
Third, the obtained homogeneous mixture was sonicated for 30 min after transferring them into a clean 10-ml beaker with the frequency of 20 kHz using ultrasonication bath.
After the heat shock, 30 synchronized larvae (based on the time of molting) from each group were placed into a clean 200 ml beaker with 150 ml distilled water and were fed the same amount of food.
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CEO of Professional Science Editing for Scientists @ prosciediting.com