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The concentration used for this study was 50 ppm of dye.
In order to determine the decolorization kinetic, Kirk's media was employed, with 200 ppm of dye, during 21 days at 25 °C and 150 rpm.
The culture was carried out in Erlenmeyer flasks with 50 mL of malt extract liquid media, 200 ppm of dye and an inoculum of four cylinders from the fungus.
In addition to this, the dye removal efficiency was also examined by a CDI flow cell for the solution containing 10 ppm of dye and 500 ppm of Na2SO4.
The effect of dye concentration on photodegradation rate of methyl violet was also evaluated by studying photodegradation at various concentrations (5, 10, 15, 20 and 25 ppm) of dye. Figure 7 shows the %degradation of methyl violet using constant catalyst dosage and irradiated time (15 min).
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In this effluent, the experiment's factors were: medium supplementation (10 g/L of glucose and 5 g/L of ammonium tartrate), inoculum (4 or 8 cylinders), and dilution (as received and 200 ppm of dyes, the dye concentration was calculated based in Novacron Red's original concentration).
1000 mL of 10 ppm concentration of dye was prepared as stock solution.
A stock solution of 1000 ppm of each dye was prepared and diluted with distilled water to prepare diluted standard solutions.
The rate constants for 5, 10, 20 and 30 ppm of RhB dye concentrations are estimated to be 0.228, 0.183, 0.033 and 0.009 h−1, respectively.
15 mg of photocatalyst showed excellent activity with 94% degradation under visible light and 10 mg of photocatalyst showed better activity for 10 ppm of OG dye with 96% for UV light irradiation under neutral pH.
The effect of dose is studied by varying the amount of dose from 0.1 to 1.0 g of each adsorbent in 50 ml of 100 ppm of MB dye solution.
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