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Exact(5)
This phenomenon can be attributed to the higher adsorption capability of –COO− on mineral surface as well as the stronger chelation effect formed by Ca2+ and –COO−.
They spread uniformly on the mineral surface as a film of densely packed coccoid cells appearing like cobblestone pavement.
The initial high concentrations of the major ions were caused by salt dissolution and/or ion desorption from mineral surface as discussed above.
The large size of Cs+ is inconsistent with the large energy of hydration needed to maintain an outer sphere complex near a charged mineral surface, as in the case of Li-montmorillonite.[12].[12]
This electrostatic effect is not seen in the adsorption of free siderophores forming mainly inner sphere complexes resulting in the location of the charge of the surface complex closer to the mineral surface as discussed above.
Similar(55)
The nonliquid water may extend out from the clay mineral surfaces as much as 60 100 Å. Hydroxyl ions are driven off by heating clay minerals to temperatures of 400° 700° C. The rate of loss of the hydroxyls and the energy required for their removal are specific properties characteristic of the various clay minerals.
As a model substance of sulfide minerals the xanthate adsorption mechanism at zinc sulfide may give information about adsorption mechanism at the other sulfide mineral surfaces as well.
Stabilization of SOM (soil organic matter) is regulated in part by sorption and desorption reactions happening at mineral surfaces, as well as precipitation and dissolution of organo-metal complexes.
This is expected because at this alkaline pH (8.27), Fe(II) could be strongly adsorbed onto the surface of illite or precipitated on mineral surfaces as insoluble species.
This study describes imbibition studies to assess the incipient interaction between selected hydrocarbons and pertinent mineral surfaces as a function of aqueous phase chemistry and microbiological perturbation.
The basic ideal of that is to regard the mineral surfaces as a functional groups carrier; therefore the surface chemical reaction can be treated in the same way as those of solution chemical reactions.
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