Synthesis and property of EPEG‐based polycarboxylate ether superplasticizers via RAFT polymerization

高效减水剂 聚合 材料科学 分散聚合 链式转移 聚乙二醇 单体 共聚物 木筏 吸附 自由基聚合 高分子化学 化学工程 可逆加成-断裂链转移聚合 乙醚 色散(光学) 聚合物 有机化学 化学 复合材料 水泥 工程类 物理 光学
作者
Xiaohong Chen,Xinde Tang,Cuizhen Zhang,Xiao Lü,Haichao Guo,Xuefan Li,Laixue Pang,Yong Yang,Fuying Dong
出处
期刊:Polymer Engineering and Science [Wiley]
卷期号:62 (9): 2769-2778 被引量:7
标识
DOI:10.1002/pen.26060
摘要

Abstract Polycarboxylate ether superplasticizers (PCEs) with comb‐shaped molecular structures have attracted considerable attention in the area of admixtures for construction engineering. However, there are some contradictions in studying the relationship between the molecular structure and property of PCE due to its random structure based on traditional free radical polymerization, which is confused for designing and developing novel PCEs. In this article, a series of reversible addition fragmentation chain transfer (RAFT) polymerization‐based polycarboxylate ether superplasticizers (RPCs) were prepared by the copolymerization of acrylic acid (AA) and ethylene‐glycol monovinyl polyethylene glycol (EPEG). The chemical structure and composition of RPCs were characterized and their adsorption behavior and dispersion properties were conducted. The results demonstrate that the molecular weights of RPCs do not vary significantly with prolonging reaction time, and the actual monomer ratio in RPCs displays a significant change to the feed one due to the monomer reactivity and conversion at higher reaction temperature, which is different from conventional free radical polymerization. The dispersion and adsorption properties of RPCs to cement were evaluated by slurry fluidity tests and total organic carbon (TOC) experiments. The effect of polymerization temperature and time on the dispersion ability has been systematically studied. The results indicate that the dispersion ability and adsorption capacity of RPCs are closely related to their molecular structures. The dispersion ability of RPCs were enhanced with increasing carboxyl group density in a certain range of monomer molar ratios (≤6:1). This study will provide a new platform for designing and developing high‐performance and rational cost‐effective superplasticizers with well‐defined structure and controlled molecular weight.
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