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IN-SITU XRD INVESTIGATION OF OPC HYDRATION

机译:OPC水化的原位XRD研究

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Rietveld+ calculations of XRD pattern of hydrated OPC pastes are leading to repeatablernresults with true quantitative approach. The first hydration product after stirringrncement powder with water (after 5 min) is Ettringite, with about 10 ma.-% with respectrnto the wet cement paste. C3A, C4AF, and sulfate carriers are decreasing at thernsame time. During the next 2.5 h no significant change in quantitative phase compositionrncould be observed. After about 8.1 h a significant content of Portlandite wasrnobserved. Consequently an increasing amorphous content of CSH phase and a decreasingrncontent of Alite was determined. At the same time C3A and Anhydrite arerndecreasing due to formation of more Ettringite. Until 19 h hydration is continuing andrnleading to an Ettringite content of about 18 ma.-% together with increasing Portlanditernand CSH contents. Belite content is not changing during the hydration until 19.1 h.rnApproximately 45 ma.-% of the paste are hydrated after 19 h. The development ofrnthe phase content is correlating very well with heat flow from calorimetric investigations.rnThe first heat flow maximum correlates with hydration of calcium sulfates andrncalcium aluminates/ferrites. The second heat flow maximum indicates the simultaneousrnhydration of calcium sulfates, calcium aluminates/ferrites and Alite. Crystallinityrnof Ettringite is improved during hydration time. Lattice parameters of Ettringite show arnshift from CO3rn2-/OH-/Fe3+ containing solid solutions towards purernC3A*3CaSO4*32H2O during hydration time.
机译:水合OPC糊剂的XRD图的Rietveld +计算可通过真正的定量方法获得可重复的结果。用水搅拌粉末后(5分钟后)的第一个水合产物是钙矾石,其相对于湿水泥浆约占10%。在相同的时间,C3A,C4AF和硫酸盐载体正在减少。在接下来的2.5小时内,未观察到定量相组成的显着变化。约8.1小时后,观察到大量的硅酸盐。因此,确定了CSH相的无定形含量增加和Alite的含量减少。同时,由于形成更多的钙矾石,C3A和无水石膏逐渐减少。直到水化持续19 h为止,导致钙矾石含量约为18 ma .-%,同时增加了Portlanditern和CSH含量。在水合期间,贝氏体的含量不会改变,直到19.1小时为止。在19小时后,约有45 ma .-%的糊状物被水合。相含量的发展与量热研究的热流有很好的相关性。第一个热流的最大值与硫酸钙和铝酸钙/铁氧体的水合有关。第二个热流最大值表明硫酸钙,铝酸钙/铁氧体和Alite同时脱水。在水化期间,结晶性钙矾石得到改善。钙矾石的晶格参数显示在水合作用期间从含CO3rn2- / OH- / Fe3 +的固溶体向纯rnC3A * 3CaSO4 * 32H2​​O的方向偏移。

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