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Inhibition efficiency increases as adsorption increases.
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At low pressure, the hydrogen adsorption is also low, and when the pressure increases the hydrogen adsorption increases as well.
The composite index also decreases as the surfactant adsorption increases.
The utilization efficiency decreases as the surfactant adsorption increases.
CH4 formation selectivity becomes higher as H2O vapor adsorption increases due to the greater concentration of OH groups or hydrophilicity of the material [4].
This is consistent with a model where the proportion of potential binding sites meeting the criterion for probe adsorption increases as the domain size decreases, as shown in Figure 6 C iii).
As we know that the physical adsorption decreases with increasing temperature, and chemical adsorption increases as the temperature increases, in solution, the molecule or adsorbate is not free like in the gas phase; it is surrounded by solvent molecules.
Our results show that phosphate adsorption is dependent on pH; adsorption increases as pH decreases.
The Γ vs E plots show that adsorption increases as potential becomes more positive.
According to results of linear shrinkage, as one expect water adsorption increases by addition of white cement.
As might be expected, adsorption increases at a given pH, ionic strength and sorbate/sorbent ratio with increasing quantities of HFO (Fig. 7).
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