To study the effect of side chains on the dispersing properties of polycarboxylate-type superplasticisers (PCs) in cement pastes, PCs with different side chains were synthesised and used as a superplasticiser for cement suspensions. The effect of side chains of PC on the zeta potential, adsorption, fluidity of the corresponding cement suspensions was investigated systematically, and total interparticle potential energy between particles was calculated. The results show that the higher the short side chains ratio of PC, the larger the adsorption amount of PC. PC with both short and long side chains presents a better dispersing property than PC with short side chains, while PC with long side chains falls in between. The maintaining dispersing ability of PC for cement particles increases as the short side chains ratio increases. The changing rule of total interparticle potential energy produced by PC is in accordance with the changing rule of dispersing property of PC in cement pastes. This indicates that the calculated results of total interparticle potential energy further support the explanation of dispersing property difference of PC in theory. This paper uses the sum of electrostatic energy and steric hindrance potential as the total interparticle potential energy to evaluate the dispersing property of PC for the first time, which is meaningful for the evaluation of dispersing property of polymer dispersant adsorbed on particle surfaces.
NotationA Hamaker constant a particle radius c equilibrium concentration of solute (mg . l À1 ) e charge of an electron F 0 , F t initial fluidity and fluidity with elapsed time h interparticle separation distance I ionic strength of the solution k equilibrium constant (l . mg À1 ) k B Boltzmann's constant Mw molecular weight of the polymer m average number of side chains in a comb-like copolymer N A Avogadros number (r 2 o ) 1=2 mean distance between the chains ends in the free solution S function of the segment density distribution S BET BET specific surface area T absolute temperature v number of adsorbed chains per unit area V elect electrostatic energy V steric steric effect V T total interparticle potential energy V vdwc van der Waals potential energy AE expansion coefficient adsorption amount (mg . g À1 ) 1maximum adsorption amount (mg . g À1