Abstract :
The adsorption isotherm of polyethyleneimine (PEI) on diatomite was studied using UV spectrophotometry, the surface of
diatomite was modified with polyethyleneimine by using impregnation method, and the trapping behavior of the modified
diatomite for phenol was investigated by using 4-aminoantipyrine (4-AAP) spectrophotometric method. The experiment results
show that negatively charged diatomite particles have very strong absorption effect for cationic macromolecule PEI, the
adsorption isotherm fits in Freundlich equation. The character that there is a maximum value after intitial sharp increase of
adsorption capacity on the adsorption curve indicates that there is strong affinity between diatomite particles and polyethyleneimine
macromolecules, and it attributes to the strong electrostatic interaction. After modification with PEI, the electric
property of diatomite particle surface changes essentially, and the isoelectric point of diatomite particles moves from pH 2.0 to
10.5. In acidic solution, phenol exists as molecular state, and the modified diatomite particles adsorb phenol through hydrogen
bond interaction. However, the hydrogen bond interaction between nitrogen atoms on PEI chains and phenol is weaker because
of high degree of protonation of polyethyleneimine macromolecules, so the adsorption quantity is lower. In basic solution,
phenol exists as negative benzene–oxygen ion, and the modified diatomite particles adsorb phenol through electrostatic
interaction. However, the electrostatic interaction between PEI and negative benzene–oxygen ion is very weak because of low
degree of protonation of polyethyleneimine macromolecules, so the adsorption quantity is much lower. The modified diatomite
particles produce very strong trapping effect for phenol in neutral aqueous solution via the cooperating of strong electrostatic
interaction and hydrogen bond interaction, and the saturated adsorption capacity can attain to 92 mg g 1.
Keywords :
polyethyleneimine , Diatomite , phenol , Surface modification , adsorption , Electrostatic interaction , Hydrogen bond interaction