An in situ nuclear magnetic resonance spectroscopy (NMR) technique is used to monitor the aqueous-phase copolymerization kinetics of methacrylic acid (MAA) and poly(ethylene glycol) methyl ether methacrylate (PEGMA) macromonomers. In particular, the study analyses the effect of the number of ethylene glycol (EG) groups along the lateral chains of PEGMA and is carried out under fully ionized conditions of MAA at different initial monomer ratios and initial overall monomer concentrations (5-20 wt % in aqueous solution). The composition drift with conversion indicates that PEGMA macromonomer is more reactive than MAA. Individual monomer consumption rates show that the rates of consumption of both monomers are not first order with respect to overall concentration of the monomer. The reactivity ratios estimated from the copolymerization kinetics reveal, that for the short PEGMA, the reactivity ratios r MAA and r PEGMA increase with the solids content (SC). A totally different trend is obtained for the longer PEGMA, whose reactivity ratio (r PEGMA23 ) decreases with solids content, whereas the reactivity ratio of MAA remains roughly constant.

Methacrylic acid‐co‐polyethylene glycol methacrylate (MAA‐co‐PEGMA) copolymers (also known as MPEG‐type polycarboxylate ether (PCE) superplasticizers) present comb‐shaped microstructure and they are generally used as dispersants of inorganic particles in cementitious formulations. Application properties of the PCEs strongly depend on the molecular structure and therefore accurate characterization of the microstructure is necessary to fully understand the structure–property relationship. In this work, MAA‐co‐PEGMA copolymers with various lateral size chain lengths and homogeneous copolymer compositions are synthesized by starved‐feed semibatch copolymerization. Molar mass and radius of gyration distributions and monomer sequence distribution are measured using size exclusion chromatography coupled with multi angle light scattering (SEC/MALS/refractive index, RI) and 1H and 13C NMR, respectively. Furthermore, it is proved that the experimental radius of gyration compares well with the prediction of a theoretical model for the radius of gyration that uses characteristic parameters of the microstructure of the PCEs (e.g., average molar masses). This confirms the accuracy of the measurements of the absolute molar masses for the MPEG‐type PCEs synthesized by free‐radical (co)polymerization.

Modelling and controlling the cumulative copolymer composition of the copolymerisation of water soluble monomers MAA and PEGMAS.

Polycarboxylic ethers or polycarboxylate (PCEs) are one of the most employed superplasticizers in construction. However, the understanding of their microstructure–property relationship is still incomplete. Recently, a theoretical model was proposed that relates the microstructure–conformation of the PCE to its effect on the adsorption onto cement particles and cement hydration time. In this work, the effects of a wide range of PCEs with different side chain lengths (P = 5, Group 1; P = 20, Group 2; and P = 45 and 113, Group 3) having flexible backbone worm conformation except one which has stretch backbone worm conformation (P = 113) were experimentally investigated for their effect on adsorption and cement hydration. It is found that PCEs from Group 1 show electrostatic repulsion as dispersing mechanism, unlike PCEs from Groups 2 and 3. Furthermore, the prediction of the theoretical model is also assessed for all the studied PCEs. Only Group 1 PCEs (shortest side chains) showed deviation from the theoretical predictions, and it was attributed to their different behaviors from the standard PCEs for which the theoretical model was developed.