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Mortars added with chemically inert sediment aggregates: performance assessment and microstructure changes

机译:迫击砂浆添加化学惰性沉积物聚集体:性能评估和微观结构变化

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This study investigates the influence of treated sediment aggregates (TSA) used as substitutes to natural aggregates in cement-based building materials. Microstructure in presence of TSA is identified, in order to justify observed changes in macroscopic performance (mainly mechanical properties and durability). TSA are valorized wastes derived from initially polluted marine sediments. They are subjected to a treatment patented by Solvay SA. It is composed of (1) a phosphatation phase, which creates, from raw sediments, an apatite-like mineral able to capture heavy metal components, and (2) a calcination at 650 degrees C, which eliminates organic pollutants. Efficient pollutant retention capability of TSA has been attested in former work. Their high water retention ability, low strength, high fine particles content, low pozzolanic activity and low chloride content are also known. In this study, mixing of the cement-based material (a normalized mortar) induces unavoidable TSA crushing and fine particles creation. In the introduction, we recall our main results as regards the potential effect of TSA content, curing conditions and age upon the performance of mortars substituted with water-saturated TSA. These are substituted to pure silica sand (0, 33, 66 and 100% sand volume). With reference to industrial practice, two extreme curing conditions are used, either water immersion (most favorable to cement hydration), or air curing (highly deficient curing). With more amplitude after water curing, porosity is shown to increase hugely with TSA amount, while apparent density decreases linearly. Up to 33% substitution, elastic Young’s modulus, uniaxial compressive strength and apparent gas permeability are all improved as compared to reference 0%-substitution mortar, all the more so when mortar is air-cured. Maturity is attained from 28 to 60 days curing only. Observed positive changes are attributed to the internal curing effect of watersaturated TSA, whereas negative performance evolutions, significant above 33% substitution, are attributed to TSA brittleness. Secondly, microstructure changes are investigated, in order to validate our interpretation of the observed changes in mechanical and durability performance. To this purpose, SEM observations and EDS analysis have been performed. Noticeable changes in silica sand/cement paste interface are shown qualitatively, whereby portlandite amount is lowered in presence of TSA. We also provide qualitative assessment of the sediment aggregate/cement paste interface and of the microstructure of cement paste in presence of TSA
机译:本研究研究了在基于水泥基建筑材料中用作自然聚集体的替代沉积物聚集体(TSA)的影响。确定在TSA存在下的微观结构,以证明观察到的宏观性能的变化(主要是机械性能和耐用性)。 TSA是源自初始污染的海洋沉积物的算源废物。它们经受溶剂SA专利的治疗方法。它由(1)磷酸化阶段组成,该磷酸化阶段从原料沉积物中产生磷灰石样矿物能够捕获重金属组分,(2)在650℃下煅烧,消除有机污染物。 TSA的有效污染物保留能力已在前工作中证明。还已知其高保水能力,低强度,高细颗粒含量,低火谷活性和低氯含量。在该研究中,混合水泥基材料(归一化砂浆)诱导不可避免的TSA破碎和细颗粒产生。在介绍中,我们回顾我们的主要结果,了解TSA含量,治愈条件和年龄在用水饱和TSA取代的迫击炮的潜在影响。这些被取代纯​​二氧化硅砂(0,33,66和100%砂体积)。参考工业实践,使用两个极端固化条件,水浸(最有利的水泥水合),或空气固化(耐高量耐用)。随着水固化后的更多振幅,显示孔隙率随着TSA的量而增加,而表观密度线性降低。与参考0% - 砂浆相比,全部改善了高达33%的替代,弹性杨氏模量,单轴抗压强度和表观透气性,所以当砂浆是空气固化时,就越多。成熟期仅达到28至60天固化。观察到的阳性变化归因于水域饱和TSA的内部固化效果,而负性性能进化,显着的替换为33%,归因于TSA脆性。其次,研究了微观结构的变化,以验证我们对机械和耐用性性能的观察变化的解释。为此目的,已经进行了SEM观察和EDS分析。定性示出了二氧化硅砂/水泥浆料界面的明显变化,从而在TSA的存在下降低了波特兰石的量。我们还提供对沉积物骨料/水泥浆料界面的定性评估,以及在TSA存在下水泥糊的微观结构

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