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A non-radioactive solution of approximately 1 mg/mL iodine was used for dilution to prevent 124I from sticking to the walls.
Over a 40-day period, 64% of the PCE was removed by flushing the cell with an alcohol solution of approximately 70% ethanol and 30% water.
US Patent No. 4130627 (1978) describes the alkaline leaching method where in the process takes place in an aqueous alkali solution of approximately pH 13, using NaOH, to form an aqueous CFA blend.
This comparison showed that the ranges of LAC produced by both methods are equivalent with an increase in LAC of the mixed solution of approximately 2% over the range of 0 66 mM.
A small amount of the compounds were dissolved in a solution of approximately 2.5 m m AgBF4 in MeOH.
The BGJ medium consists of an aqueous solution of approximately 50 ingredients including inorganic salts, glucose, amino acids, vitamins, and antibiotics.
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In this scenario, 5% pH -3 solution +95% pH 7 solution results in a solution pH of approximately 0.5, but only contributes 1.7 cal to the solution (i.e., enough to raise 1 liter of water 1.7°C).
Briefly, PHA solutions of approximately 1.0 g L−1 were prepared by dissolution in chloroform and passed through a syringe filter (0.45 μm PTFE).
Fibers of AmelF3 protein were generated by extruding solutions of approximately 3% AmelF3 and less than 0.4% SDS through capillary tubing into an aqueous methanol coagulation bath.
Solvents were either H2O (solvent A) and CH3CN (solvent B), at a flow rate of 1.0 mL min−1 eluting with a gradient 5 80%% B over 60 min. All injections were 50 μL of aqueous solutions of approximately 20 30 μ m of each platinum(IV) complex.
Then, the tube solution consisted of approximately 32 mg/L of individual C-SWCNT in a 0.6 wt% aqueous sodium dodecyl sulfate (SDS) solution.
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