Retardation mechanisms and microstructure evolution of triclinic tricalcium silicate induced by three different organic phosphonic acids

IF 13.1 1区 工程技术 Q1 CONSTRUCTION & BUILDING TECHNOLOGY
Xingdong Lv , Zhuofan Gao , Lu Yang , Fazhou Wang
{"title":"Retardation mechanisms and microstructure evolution of triclinic tricalcium silicate induced by three different organic phosphonic acids","authors":"Xingdong Lv ,&nbsp;Zhuofan Gao ,&nbsp;Lu Yang ,&nbsp;Fazhou Wang","doi":"10.1016/j.cemconres.2025.108041","DOIUrl":null,"url":null,"abstract":"<div><div>This paper investigated the inhibition effects and mechanisms of organic phosphonic acids (OPAs) with distinct functional groups on triclinic tricalcium silicate (C<sub>3</sub>S) clinker hydration. In particular, the effects of three representative OPAs, namely ATMP, HEDP, and PBTC on adsorption/complexation behavior, hydration products, and microstructure characteristics of C<sub>3</sub>S clinker were studied. OPAs retardation of the C<sub>3</sub>S clinker hydration was governed by synergistic interactions of electrostatic adsorption, and cationic complexation, potentially involving intermolecular self-polycondensation. ATMP primarily relied on Ca<sup>2+</sup> complexation through its [–C-PO(OH)<sub>2</sub>] groups, forming low-solubility precipitates that inhibited hydration. HEDP combined strong complexation with intermolecular self-polycondensation, driven by its [–C–PO(OH)<sub>2</sub>] and (–OH) groups, generating dense three-dimensional polymers that enhanced steric hindrance, while PBTC operated through surface adsorption and self-polycondensation. The revealed retardation efficiency hierarchy (HEDP &gt; PBTC &gt; ATMP) arose from functional group synergy: the maximal inhibition was provided by synergy of [–C–PO(OH)<sub>2</sub>] and (–OH) groups, a weaker one-by that of [–C–PO(OH)<sub>2</sub>] and (–COOH) groups, while isolated [–C–PO(OH)<sub>2</sub>] groups had the minimal retarding capacity.</div></div>","PeriodicalId":266,"journal":{"name":"Cement and Concrete Research","volume":"199 ","pages":"Article 108041"},"PeriodicalIF":13.1000,"publicationDate":"2025-09-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cement and Concrete Research","FirstCategoryId":"5","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0008884625002601","RegionNum":1,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CONSTRUCTION & BUILDING TECHNOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

This paper investigated the inhibition effects and mechanisms of organic phosphonic acids (OPAs) with distinct functional groups on triclinic tricalcium silicate (C3S) clinker hydration. In particular, the effects of three representative OPAs, namely ATMP, HEDP, and PBTC on adsorption/complexation behavior, hydration products, and microstructure characteristics of C3S clinker were studied. OPAs retardation of the C3S clinker hydration was governed by synergistic interactions of electrostatic adsorption, and cationic complexation, potentially involving intermolecular self-polycondensation. ATMP primarily relied on Ca2+ complexation through its [–C-PO(OH)2] groups, forming low-solubility precipitates that inhibited hydration. HEDP combined strong complexation with intermolecular self-polycondensation, driven by its [–C–PO(OH)2] and (–OH) groups, generating dense three-dimensional polymers that enhanced steric hindrance, while PBTC operated through surface adsorption and self-polycondensation. The revealed retardation efficiency hierarchy (HEDP > PBTC > ATMP) arose from functional group synergy: the maximal inhibition was provided by synergy of [–C–PO(OH)2] and (–OH) groups, a weaker one-by that of [–C–PO(OH)2] and (–COOH) groups, while isolated [–C–PO(OH)2] groups had the minimal retarding capacity.
三种不同有机膦酸对三斜型硅酸三钙的缓凝机理及微观结构演变
研究了不同官能团的有机膦酸(OPAs)对三斜硅酸三钙(C3S)熟料水化的抑制作用及其机理。特别研究了三种具有代表性的OPAs,即ATMP、HEDP和PBTC对C3S熟料吸附/络合行为、水化产物和微观结构特征的影响。OPAs对C3S熟料水化的阻滞是由静电吸附和阳离子络合的协同作用控制的,可能涉及分子间的自缩聚。ATMP主要依靠Ca2+络合通过其[-C-PO (OH)2]基团,形成低溶解度的沉淀物,抑制水合作用。HEDP在其[-C-PO (OH)2]和(-OH)基团的驱动下,结合了强络合作用和分子间自缩聚作用,生成了致密的三维聚合物,增强了位阻,而PBTC则通过表面吸附和自缩聚作用。HEDP > PBTC >; ATMP是由官能团的协同作用引起的:[-C-PO (OH)2]和(-OH)基团的协同作用最大,[-C-PO (OH)2]和(-COOH)基团的协同作用较弱,而分离的[-C-PO (OH)2]基团的阻滞能力最小。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Cement and Concrete Research
Cement and Concrete Research 工程技术-材料科学:综合
CiteScore
20.90
自引率
12.30%
发文量
318
审稿时长
53 days
期刊介绍: Cement and Concrete Research is dedicated to publishing top-notch research on the materials science and engineering of cement, cement composites, mortars, concrete, and related materials incorporating cement or other mineral binders. The journal prioritizes reporting significant findings in research on the properties and performance of cementitious materials. It also covers novel experimental techniques, the latest analytical and modeling methods, examination and diagnosis of actual cement and concrete structures, and the exploration of potential improvements in materials.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信