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However, when it is solubilised in micelles of sodium dodecyl sulphate, which are bacterial membrane-mimetic, the α-helical content increases to ca. 35 40%.
Under optimal reaction conditions at 2 °C, the faradaic efficiency (FE) for converting CO2 to methane (CH4) on a Cu electrocatalyst increases to ca. 50% while ethylene (C2H4) decreases to ca. 10%.
However, the average diameter of α-Fe2O3 microspheres in sample 6 increases to ca. 260 nm, higher than that of sample 1 (170 nm), implying that higher microwave-hydrothermal temperature will produce α-Fe2O3 microspheres with larger size.
At the excitonic peak, the responsivity reaches 230 A/W for an illumination intensity of 30 μW/cm and increases to ca. 450 A/W when the light intensity is reduced to below 1 μW/cm.
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As the surface was approached, the pH over the zinc layer decreased slightly from ca. 5.6 in the original bulk solution, while the pH over the steel surface distant from the zinc layer increased to ca. 11.5.
We found that the WCA of highly ordered pyrolytic graphite (HOPG) was 64.4 ± 2.9° when measured within 10 s after exfoliation in air and increased to ca. 90° after exposure to the ambient air.
Membranes with total ion-exchange capacities above 6 meq/g showed proton conductivities of approximately92 mS/cm at 25 °C and 100% relative humidity increasing to ca.150 mS/cm at 140 °C.
Transmission electron microscopy image of the as-prepared Pt Sn/C catalyst reveals a mean particle diameter of ca. 5.8 nm with a relatively narrow size distribution and the particle size increased to ca. 20 nm when heat-treated at 500 °C due to agglomeration.
Below 51 mm, Mn2+ and Fe2+ tailed off, while the FeIIIL signal increased to ca. 75 nA.
Mn2+ appeared at 9 mm and slowly increased to ca. 30 μm at a depth of 51 mm.
The fluorescence intensity of the monomer emission of 2 linearly decreased as the concentration of Cu2+ increased to ca. 1 × 10-4 M (10 equiv).
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