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Electrolyte decomposition during the electrochemical charging processes increased with Ni substitution.
As shown in Table 1, the PCP degradation rate in both processes increased with increasing pH.
These findings designate that under the selected condition, the oxidation of PCP in both processes increased with the increase of initial pH and reaction time.
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The apparent activation energy of all considered processes increases with sulfur content in the catalyst.
The saturation time of the adsorption process increased with the thickness of the porous layer.
The difference in the permeate TDS between NF NF and NF BW process increased with increasing the feed salinity.
The rate of the corrosion process increased with increasing in molar mass of naphthenic acid, reaching a maximum value in the presence of CHPA acid (C9), and then decreased.
The rate of the forward transfer process increased with decreasing pH and ionic strength whilst the opposite conditions (i.e. high pH and ionic strength) favoured the rapid back extraction of protein from the reverse micellar phase.
Level of total sugars production in saccharification process increased with increase in incubation time.
The efficiency of the process increased with an increase in solution temperature, showing that the overall ozonation reaction is endothermic.
The efficiency of the process increased with an increase in the solution temperature, and the reason of this trend was explained in the previous paragraph.
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