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As a chromogenic reagent, the solution of methyl violet mainly shows purple.
For dissolution of extracts, an aqueous solution of methyl hydroxypropyl cellulose (MHPC, 0.5 %, methocel™ E4M prem) was prepared.
The resist was developed in a 1 3 solution of methyl isobutyl ketone (MIBK) and isopropanol (IPA).
After writing, the patterned substrates were developed in a solution of methyl isobutyl ketone and isopropyl alcohol (volume ratio of 1 3) for 30 s.
Next, a solution of methyl propiolate (2.7 mL, 30 mmol) in anhydrous ether (10 mL) was added dropwise, over a period of about 60 min.
The solution of methyl orange in deionized water with a concentration of 5 ppm was chosen as a matter of photodegradation.
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The P deposit was formed by impregnating carbon/carbon composite samples with methanol solution of methyl-phosphoric acid or phosphorus oxychloride and heating at ca. 600 °C.
A solution of methyl-2- 2-thiocyanatoacetamido)benzoate methyl-2- 2-thiocyanatoacetamido methyl-2- 2-thiocyanatoacetamido, 10 methyl-2- 2-thiocyanatoacetamido allowed to cool.
A solution of methyl-4- 2-chloroacetamido)benzoate methyl-4- 2-chloroacetamidommonium methyl-4- 2-chloroacetamidoetone or absolute methyl-4- 2-chloroacetamidoed for 6 h and allowed to cool.
Surface hydrophobisation was carried out by means of: a solution of methyl-silicone resin with high VOC content, aqueous emulsion from methyl-silicone resin in potassium hydroxide and low-molecular alkyl-alkoxy-silane in an organic solvent.
A solution of methyl-4- 2-chloroacetamido)benzoate methyl-4- 2-chloroacetamidommonium methyl-4- 2-chloroacetamidothanol (30 methyl-4- 2-chloroacetamidoor refluxing 4 in MeOH for 6h then the reaction mixture was allowed to cool down to room temperature.
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