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For computational purposes, concentrations at t = −15 min were taken as concentration at zero time.
When dissolved in polyethylene oxide) (PEO), the alkali metal imides LiN CF3SO2 2 (LiTFSI), NaN CF3SO2 2 (NaTFSI) and KN CF3SO2 2 (KTFSI) yield rubbery electrolytes over a wide range of concentrations at T > 50 °C.
Dependence of the thermal noise in the MCT QW with molar composition x = 0.06 on the well width, for different electron concentrations at T = 77 K Fig. 4 Dependence of the thermal noise on electron concentration.
To control for potential differences in water quality parameters between treatments, dissolved oxygen (mg L−1) and pH were also measured at selected temperatures and Cu concentrations at t = 0 and t = 24h for treatments containing 10 day old A. millepora larvae.
The ODE system was numerically solved and the values for concentrations at t = 999999 were taken as steady state values.
We estimated the rate parameters (k → ) and the initial metabolite concentrations at t = 0 (X → 0 ) from the training data.
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Three-layer ANN architecture was trained using an experimental database and the concentration at t time over initial concentration (C/Co) was calculated as output variable.
Figure 3 shows that glucose concentration at T is higher when the injection dose σ is smaller and the injection period τ is longer.
During the CO2 photoreduction reaction, the increase of CH4 concentration (ppm/cm2, △CH4, which is the difference between CH4 concentration at t reaction time and the initial time) was used to evaluate the photocatalytic performance.
The solution is characterized by the (adimensional) concentration u ( μ, t ) = ( c − c init ) / c inlet, being c the dimensional concentration, c init the initial dimensional concentration (at t = 0 ), and inlet the dimensional concentration imposed at the inflow (at every time step).
The synthesis/hydrolysis (S/H) ratio was calculated according to the following equation: ({text{S/H ratio = }}frac{{C{text{p}} - {text{t}}}}{{C{text{ester}} - 0- C{text{ester}} - {text{t}} - C{text{p}}text{text{t}}}}), where C p−t, C ester−0, and C ester−t are the N-bromoacetyl-7-ACA concentration at t h, the bromoacetate concentrations at 0 and t h, respectively.
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