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The samples were placed in a crucible and heated in pure nitrogen (inlet flow rate of 20 ml/min) to a set temperature of 900 °C.
The nanocrystal growth was carried out without an electric field applied in a multipurpose oven for 1 3.5 h periods at a set temperature of 85 °C.
The experimental set up was run during winter inside a 2350 m2 plastic greenhouse in the West of France for a set temperature of 16 °C.
Then, the Erlenmeyer flask was shaken (150 rpm) in an incubator shaker with a set temperature of 25 °C for a period of 24 h to reach adsorption equilibrium.
The fed-batch experiments were conducted in 1 L bioreactor (BioFlo110, New Brunswick Scientific Co., Inc., Canada) with a final working weight of 0.6 kg at a set temperature of 35˚C and 150 rpm.
In groups where HT was applied (III and IV), a feedback control system involving the measurement of temperature in the tumour centre with a thermocouple (∅ 250 μm; type 2ABAc, Philips, Kassel, Germany) was used to heat tumours (0.4°C min−1) to a set temperature of 43°C.
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It was clear from the release measurements that a setting temperature of 60°C resulted in slower release, as compared to setting at room temperature; this was observed for all three investigated Al/Si ratios of the precursor powder.
Clearly, at a set temperature, increased time of incubation represents increased thermal energy input, thus greater cross-link reversal.
All relaxation measurements were conducted at a spinning speed of 10 kHz (±20 Hz) and a nominal set temperature of 25 °C.
Kamaboko gel having setting temperature of 25°C.
Particularly given a set point temperature of 0 °C and a leakage rate of 10%, R-410A determines the best environmental performance.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com