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Hybrid binders based on alkali sulfate-activated Portland clinker and metakaolin

机译:基于碱硫酸盐活化的波特兰熟料和甲霉素的杂种粘合剂

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The development of hybrid binders based on combinations of conventional Portland clinkers and alkali-activated aluminosilicates as a mean of improving the sustainability of the cement production and reducing CO2 emissions is currently attracting increasing interest. The normal approach in these binders, as with pure alumino-silicate systems, is to use alkali silicate or hydroxide activators; although the production of these chemicals is energy intensive compared to alkali sulfates. New alkali-activated binders in the system Na2SO4 (NS) – white Portland clinker – metakaolin (MK) have been synthesized by designing the precursor mixes based on the desired final phase assemblages. Compared to conventional blended Portland cements, these systems have the added advantage of allowing the use of much higher amounts of supplementary cementitious materials (SCMs) (up to 60% MK of total binder) without any loss in performance. The activation-hydration products of these binders formulated with different contents of NS and MK/(MK+limestone) ratios have been primarily assessed by 29Si and 27Al MAS NMR along with powder X-ray diffraction (XRD) at 28 days of curing. 29Si MAS-NMR shows the formation of silicate chain structures with Al substitution (Q2(1Al) sites) within the binder. The incorporation of tetrahedrally coordinated Al in the C-S-H phase is also observed by 27Al MAS NMR. These spectra also reveal that at lower levels of NS addition, AFm phases (e.g. monosulfate and/or monocarbonate) and AFt phases (ettringite) are the main aluminate phases formed in approximately equal proportions, whereas an increased NS content in the binder leads to the formation of additional ettringite at the expense of the AFm phases. Formation of an X-ray amorphous aluminosilicate gel is also identified in all samples, and the content of this phase increases as a function of reaction time and the content of NS in the binder, which is associated with the activation of the MK included in the system.
机译:基于常规波特兰熟料和碱活化硅硅酸盐的组合的杂交粘合剂的开发作为改善水泥生产可持续性和减少二氧化碳排放的平均值目前吸引了越来越令人利益。与纯铝硅酸盐系统一样,这些粘合剂中的正常方法是使用碱性硅酸盐或氢氧化物活化剂;尽管与碱硫酸盐相比,这些化学品的生产是能量密集。通过基于所需的最终相位组合设计前体混合物,已经合成了系统Na2SO4(NS) - 白色波特兰熟料 - Metakaolin(MK)中的新碱活化粘合剂。与传统的混合波特兰水泥相比,这些系统具有额外的优点,可以使用更高量的辅助水泥材料(SCM)(高达60%的总粘合剂)而没有性能的损失。用不同含量的NS和MK /(MK +石灰石)比配制的这些粘合剂的活化 - 水合产物主要通过29SI和27AlMAS NMR进行评估,以及在28天的固化下的粉末X射线衍射(XRD)。 29SI MAS-NMR显示粘合剂内的Al取代(Q2(1Al)位点的硅酸盐链结构的形成。通过27AlMAS NMR,还观察到C-S-H相中的四面体协调Al。这些光谱还表明,在较低水平的NS加法下,AFM相(例如单硫酸盐和/或一甘料酸盐)和尾剂相(Ettringite)是以大致相等的比例形成的主要铝酸盐相,而粘合剂中的NS含量增加导致以牺牲AFM阶段为代价形成额外的Ettringite。在所有样品中也鉴定了X射线非晶硅铝酸盐凝胶的形成,并且该相的含量随着反应时间的函数和粘合剂中NS的含量而增加,这与包括在内的MK的激活相关联系统。

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