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The composites were mixed with an optimum volume of neutral phosphate buffer maintaining a solid/liquid ratio of 1.08 g/ml and thoroughly mixed and filled in a syringe to fill up at the site of injury or casted by filling up in metallic moulds to produce pellet-shaped samples or coated as slurry on surface of cover slips.
Then, the PPy/VGCF composites were mixed with activated carbons (AC) at various mixing ratios.
Obtained powders of the composites were mixed with powder of strontium oxide (1 wt.%).
In the case of alkali activation, C/SiO2 composites were mixed with scaly either KOH or NaOH (without additional water).
The composites were mixed with acetylene black (15 wt.%) and dispersed in 0.5 mL of anhydrous ethanol solution by sonication for 5 min.
The RGO/ZnO nanocrystals composites were mixed with wax with different mass fraction (5, 10, 15, 20 wt%) to examine the dielectric and microwave absorption properties.
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The recycledcopper-filled epoxy composite was mixed using a mechanical stirrer.
The MB solution and the TiO2/PAA/PTFE composite membrane were mixed on a magnetic stirring machine and remained in dark for an hour to establish a MB solution adsorption desorption equilibrium on the membrane before light irradiation.
At first, the appropriate amounts of Y2O3 were dissolved in nitric acid; then, the zirconium and yttrium salts (in case of matrix material) and zirconium, aluminum, and yttrium salts (in case of composite material) were mixed with a propeller stirrer for 30 min and were subsequently added to an aqueous solution of the precipitant (25% NH4OH) with constant stirring.
Prepared composite NPs (100 mg) were mixed with HCl solution (600 ml, 1 N) and incubated for 18 h at room temperature.
The nano-HAP/collagen I composite powder material and PLGA were mixed with sodium chloride (NaCl) at a certain proportion and dissolved in acetone as the substratum cartilage material.
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