Ezzat Metwally, Xu Xiaowen, El Cheikh Khadija, Lesage Karel, Hoogenboom Richard, De Schutter Geert
Ghent University, Department of Structural Engineering, Magnel Laboratory for Concrete Research, Technologiepark-Zwijnaarde 60, 9052 Ghent, Belgium; Supramolecular Chemistry Group, Centre of Macromolecular Chemistry (CMaC), Department of Organic and Macromolecular Chemistry, Ghent University, Krijgslaan 281-S4, 9000 Ghent, Belgium.
Supramolecular Chemistry Group, Centre of Macromolecular Chemistry (CMaC), Department of Organic and Macromolecular Chemistry, Ghent University, Krijgslaan 281-S4, 9000 Ghent, Belgium.
J Colloid Interface Sci. 2019 Oct 1;553:788-797. doi: 10.1016/j.jcis.2019.06.088. Epub 2019 Jun 26.
Polycarboxylate ether (PCE) comb-copolymers are widely used as water reducing agents in the concrete industry while maintaining a high fluidity via the polymer adsorption to the cement particles. PCE copolymers with a broad range of structures are well established by Free radical polymerization, however, understanding the structure-property relationship is still complex due to the high polydispersity of PCE copolymers prepared by conventional polymerization. The influence of different structural parameters using well-defined polymeric structures is yet to be explored.
In this study, two different types of comb-like random copolymers, namely polycarboxylate ether (PCE; poly(oligo(ethylene glycol) methyl ether methacrylate/methacrylic acid)) and polysulfonate ether (PSE; poly(oligo(ethylene glycol) methyl ether acrylate/sodium 4-styrenesulfonate)), were synthesized by RAFT polymerization to enable the synthesis of polymers with controlled features. The effect of charge types and side chain lengths on the adsorption, rheology, and dispersing ability of cement pastes have been studied.
RAFT polymerization could be used to prepare PCE random copolymers with good control over the polymer molecular weight and narrow polydispersity (Đ < 1.3). Results revealed that the ζ-potential values depend on both the charge type and side chain lengths. Copolymers containing SO exhibited higher absolute negative ζ-potential values than COO while PCE copolymers with shorter side chains developed higher absolute negative ζ-potential values. On the other hand, the adsorption study demonstrated that decreasing the side chain lengths lead to higher adsorption of PCE copolymers while Copolymers with COO groups were found to be adsorbed more than SO counterparts. These results are further confirmed with the rheological studies and it is found that the shorter the side chain, the lower the yield stress and the higher the dispersion of cement pastes but to a limited effect. Additionally, the charge types have a major influence on the performance of superplasticizers. This study could make further progress in establishing superplasticizers with controlled architectures for better performance.
聚羧酸醚(PCE)梳状共聚物在混凝土行业中被广泛用作减水剂,通过聚合物吸附到水泥颗粒上保持高流动性。通过自由基聚合已很好地制备了具有广泛结构的PCE共聚物,然而,由于传统聚合制备的PCE共聚物具有高多分散性,理解结构-性能关系仍然很复杂。使用明确的聚合物结构来研究不同结构参数的影响尚未得到探索。
在本研究中,通过可逆加成-断裂链转移(RAFT)聚合合成了两种不同类型的梳状无规共聚物,即聚羧酸醚(PCE;聚(低聚(乙二醇)甲基醚甲基丙烯酸酯/甲基丙烯酸))和聚磺酸醚(PSE;聚(低聚(乙二醇)甲基醚丙烯酸酯/4-苯乙烯磺酸钠)),以实现具有可控特性的聚合物的合成。研究了电荷类型和侧链长度对水泥浆体吸附、流变学和分散能力的影响。
RAFT聚合可用于制备对聚合物分子量有良好控制且多分散性窄(Đ<1.3)的PCE无规共聚物。结果表明,ζ电位值取决于电荷类型和侧链长度。含SO的共聚物比含COO的共聚物表现出更高的绝对负ζ电位值,而侧链较短的PCE共聚物产生更高的绝对负ζ电位值。另一方面,吸附研究表明,侧链长度的减少导致PCE共聚物的吸附增加,同时发现含COO基团的共聚物比含SO基团的共聚物吸附更多。流变学研究进一步证实了这些结果,发现侧链越短,水泥浆体的屈服应力越低,分散性越高,但效果有限。此外,电荷类型对高效减水剂的性能有重大影响。本研究可为建立具有更好性能的可控结构高效减水剂取得进一步进展。