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It was noted that an elevated ionic strength due to NaCl did not significantly interfere the binding of dye molecules to adsorption sites on the biomass.
According to Panda et al. 2009, dye adsorption on solid surface may be explained by two distinct mechanisms; (1) an initial rapid binding of dye molecules on the adsorbent surface followed by (2) relatively slow intra-particle diffusion.
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The binding affinity of dye molecules is indicated by high k L values.
Thus, −COOH group is a promising fixed group of dye molecules for the preparation of dye-sensitized solar cells (DSSCS).
The adsorption of dye molecules is pH dependent.
However, encapsulation of dye molecules inside SWCNTs completely quenches dye PL, thus allowing measurement and analysis of their Raman spectra.
The use of AIE dyes, however, requires the significant accumulation of dye molecules on the cells to cause aggregation.
In addition, we demonstrated the strong influence of dye molecules on the ablation threshold.
The visible absorption spectra of aqueous dye solutions changed with the addition of the nonionic surfactants, but further addition of PVP had little effect on the spectra, indicating that the strong binding of the dye molecules with the nonionic surfactant micelles is maintained even in the presence of PVP.
And when it stained with DNA binding dye, dye molecules are intercalate in between loop of extruded DNA and become visualized under fluorescent microscope.
The probability of binding x azo dye molecules with the QD surface is p ( t, x ) = e - t t x x !, (2) .
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