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Binding of external chlorides by cement pastes.

机译:水泥浆与外部氯化物的结合。

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摘要

Chloride-induced reinforcement corrosion is the dominant cause of premature deterioration of reinforced concrete structures worldwide. The need to quantify the durability of new and existing structures led to the development of service life prediction models. This requires a clear understanding of the mechanisms of chloride penetration into concrete cover. This research looks into chloride binding when chlorides are introduced after the hydration of cement.; Highlights of this research include the X-ray diffraction (XRD) results which provide insight into some mechanisms of chloride binding. They show that several calcium aluminate hydrates (C-A-H), including monosulphate, convert to Friedel's salt. The monosulphate converts Kuzel's salt at low concentrations before transforming into Friedel's salt at higher concentrations. Evidence suggests that ettringite starts converting to Friedel's salt at high chloride concentration. Friedel's salt peaks kept increasing at chloride exposures above 1.0 M, indicating that chemical binding is not exhausted at low chloride concentrations.; The results indicate the chloride binding capacity of cement paste results from the contribution of hydrates of different cement phases. The C3 A has a strong effect on chloride binding, especially at high chloride concentrations (1.0– 3.0 M). Evidence from synthetic compound pastes and cement pastes indicate that C4AF, C3S, and C 2S bind chlorides and significantly contribute to the binding capacity. The binding isotherms of cement pastes can be predicted from the chemical composition of cements.; The results show that chloride binding isotherms are non-linear, and the Freundlich isotherm is the best fit in the chloride concentration range 0.1 M–3.0 M. In general, the partial replacement of cement with fly ash, ground granulated blast furnace slag (GGBFS), or metakaolin, increased chloride binding. Partial replacement with silica fume reduced chloride binding. An increase in the pH (13–14) of the storage solution reduced chloride binding. The presence of sulphate ions in the storage solution at 0.1 M concentration reduced chloride binding. Pre-carbonation of cement pastes greatly reduced chloride binding. An increase in temperature between 7°C and 38°C reduced chloride binding at 0.1 M chloride exposure, but increased it at 3 M exposure.
机译:氯化物引起的钢筋腐蚀是全世界钢筋混凝土结构过早劣化的主要原因。量化新结构和现有结构的耐久性的需求导致了使用寿命预测模型的发展。这需要清楚地了解氯化物渗透到混凝土表层的机理。这项研究研究了在水泥水合后引入氯化物时的氯化物结合。这项研究的重点包括X射线衍射(XRD)结果,可深入了解氯化物结合的某些机理。他们表明,包括单硫酸盐在内的几种铝酸钙水合物(C-A-H)可以转化为弗里德尔盐。一硫酸盐将低浓度的库兹尔盐转化成高浓度的弗里德尔盐。有证据表明,钙矾石在高氯化物浓度下开始转化为弗里德尔盐。当氯化物暴露超过1.0 M时,弗里德尔的盐峰持续增加,这表明在低氯化物浓度下化学结合不会消失。结果表明水泥浆的氯离子结合能力是由于不同水泥相的水合物的贡献所致。 C 3 A对氯离子的结合有很强的作用,尤其是在高氯离子浓度(1.0-3.0 M)下。合成糊料和水泥糊料的证据表明,C 4 AF,C 3 S和C 2 S结合氯化物,并显着地促进了氯化物的形成。结合能力。水泥浆的结合等温线可以由水泥的化学组成来预测。结果表明,氯化物结合等温线是非线性的,弗氏树脂等温线最适合氯浓度范围为0.1 M–3.0M。通常,用粉煤灰,磨碎的高炉矿渣(GGBFS)部分替代水泥)或偏高岭土,增加氯离子的结合。用硅粉部分替代可减少氯离子的结合。储存溶液的pH值升高(13-14)会减少氯离子的结合。储存溶液中浓度为0.1 M的硫酸根离子的存在会降低氯离子的结合。水泥浆的预碳酸化大大降低了氯离子的结合。温度在7°C至38°C之间升高会降低0.1 M氯化物暴露下的氯离子结合,但在3 M暴露下会增加。

著录项

  • 作者

    Zibara, Hassan.;

  • 作者单位

    University of Toronto (Canada).;

  • 授予单位 University of Toronto (Canada).;
  • 学科 Engineering Civil.
  • 学位 Ph.D.
  • 年度 2001
  • 页码 320 p.
  • 总页数 320
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 建筑科学 ;
  • 关键词

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