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This modification was realized by a hydrothermal treatment following a Mg2+ or Ca2+ ion-substitution process.
Such modification was realized by grafting with alkanols of different chain lengths (hexanol, dodecanol and octadecanol) on the surface of starch-based films.
The surface modification was realized through the binding of the triptycene moiety onto the sidewall of SWCNTs through a π π stacking interaction, and the oligo ethylene glycol) chains extend into the water and act as dispersing agents, thus yielding an aqueous SWCNT dispersion.
It seems, however, that only a limited number of ways of plastome modification was realized in the evolutionary history of higher plants.
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In order to overcome this constraint and infiltrate the template effectively, a practical approach of centrifuge tube modification is realized by placing a small-sized tube within the original long tube.
The chemical modifications were realized with Brazilian bentonite sample, 3-aminopropyltrietoxisilane (APS) and 3,2-aminoethylaminopropyltrimetoxisilane (AEAPS), such as raw material and intercalating agents, respectively.
The activation reaction was carried out at 293 K for 2 h, while modification of APTES was realized at 293 K for 20 h.
Chemical modification of cotton was realized by grafting with glycidyl methacrylate alone or in combination with β-cyclodextrin by irradiation using fasting electron beam.
The separation was realized according to the method described by Lopez Torres et al.[ 82] with some modifications.
As O-GlcNAc modification in protein occurs at serine/threonine residues, the potential for interplay between serine/threonine phosphorylation and O-GlcNAc modification has been realized very early on [ 4].
The modification can be realized by doping foreign elements, coupling UV-active photocatalysts with narrow band gap semiconductors, as well as forming inorganic-organic hybridization [14 30].
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