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On the basis of recent molecular simulation and experimental studies, we discuss two possible strategies for tuning the mechanical properties of cementitious materials by modifying the bonding scheme in the hydrates at molecular level.
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Previous experience of the dam can also modify the bonding process in some species [ 19, 20].
Because it had issued most of its debt under local law, it could modify the bonds' terms however it chose.
When the HDPE surfaces are not modified, the bond shear strength is only 0.20 MPa, with a standard deviation of 14%%.
This study was expanded by Cortes et al. [9], who observed loss of activity on changing the hydantoin ring to imidazolone or imidazolidinone, by modifying the hydrogen bonding groups.
The problems of single lap joint with humidity exposure were studied by Goglio et al. [17], the main defect mechanism was the presence of bubbles filled with water at primary substrate/adhesive layer modifying the surface bonding area and thus taunting the failure.
Related to this general conclusion and based on factor analyses in multiple samples, Kendler [ 7] proposed three parenting dimensions represented by the scales Warmth, Protectiveness and Authoritarianism, when modifying the Parenting Bonding Instrument (PBI) from earlier work by Parker [ 8].
The presence of water can modify the cation bonding strength depending on the number of bonds each water molecule forms to the cations within the interstitial component.
The results indicated that hydrogen and oxygen plasma treatment modified the carbon bonding structure and the surface roughness differently.
We have designed and synthesised peptides to show how Coulombic interactions between ionizable 2,3-diaminopropionic acid (Dap) side chains can be manipulated to tune the functional pH response of the peptides to afford optimal nucleic acid transfer and have modified the hydrogen bonding capabilities of the Dap side chains in order to reduce cytotoxicity.
Class I hybrids only have weak van der Waals forces, hydrogen bonding and/or ionic bonding, whereas class II hybrids have strong covalent bonding,[ 4b] which is normally achieved by modifying the polymer so it can bond to the inorganic phase.
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