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This further confirms that the different velocities observed in solution can be attributed to differences in electrochemical potentials.
Taken into consideration the cited references and the E a value calculated from Arrhenius plots, the action of RL extract as a corrosion inhibitor for mild steel in acidic solution can be attributed to strong adsorption bond of a chemisorptive nature.
The constants k1 and k2 of the first order kinetics solution can be attributed to cell proliferation and cells switching from adherent state to the suspended state.
The SNR improvement relative to the previous experiments on NPs in solution can be attributed to the heat confinement to the cells in addition to the longer averaging time.
The gradual approach of the intraparticle pH to that of the bulk solution can be attributed to a transition from initially mass transfer-limited reaction conditions to new conditions at the end of the conversion (in which enzymatic transformation was mainly rate determining).
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The increase in the tan δ value for the calcium hydroxide solutions can be attributed to the increase in ions from calcium hydroxide and the dissociation of calcium hydroxide molecules to ions with the increase in temperature [11].
Strikingly, the low η of binary solutions can be attributed to a significant decrease in physical interactions between the chains, while strong gel strength could be attributed to an increased fraction of intermolecular cross-links and stiffened molecules as compared to gels comprised of high MW alginates.
This result can be attributed to the pH and/or the amount of metal ions in solution.
And the increase of the solution conductivity can be attributed to the increasing positive charges ionized by cationic dyes dissolved in solution.
Emission in the solid state is ∼400 times stronger than that in solution; this can be attributed to the inhibition of the excited state geometry relaxation to a non-radiative state, in the solid.
The higher ultimate recovery for the secondary ionic solution flooding can be attributed to the lower water content of the sample rocks and hence the less dilution of the ionic solution within the porous medium.
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