Valorization of a Steel Industrial Co-Product for the Development of Alkali-Activated Materials: Effect of Curing Environments

IF 1.5 Q4 MATERIALS SCIENCE, MULTIDISCIPLINARY
Arezki Sarri, M. Oualit, S. Kennouche
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Abstract

Abstract While natural resources are becoming scarce and climate change is accelerating, the recovery and recycling of wastes and by-products is an effective way to deal with the economic and ecological constraints of recent decades. The valorization of industrial by-products in civil engineering is a common practice either by their incorporation during the manufacture of Portland cements or as a partial replacement of cement during the production of concrete. The present work aims to develop waste-based alkali-activated materials WAAMs intended for civil engineering applications as a potential alternative to cement-based materials. A steel industrial by-product called commonly granulated blast furnace slag GBFS was used alone as a solid CaO-rich precursor; two alkaline activators such us sodium silicate (Na2SiO3) and sodium hydroxide (NaOH) were used separately for the production of two-part alkali-activated materials. Besides the microstructure analysis of the hardened samples, the influence of activator/precursor mass ratio, NaOH molarity, and two curing environments (Room temperature and 60°C) on the compressive strength, water accessible porosity, mass loss, and drying shrinkage were assessed. The results showed that a high Liquid/Solid ratio leads to a decrease in the compressive strength of the samples, while high NaOH molarity significantly improves the mechanical properties by reducing the porosity of the specimens. Moreover, alkaline silicate activator provides higher compressive strengths compared to the alkaline hydroxide activator, especially when the samples were cured at room temperature where a maximum 28days-compressive strength value of 105.28 MPa was achieved. For the samples activated using sodium hydroxide solution, the results revealed that their curing at 60°C promotes obtaining high initial-compressive strengths (7 days) before decreasing subsequently as a function of the curing time. As an indication, at high alkaline concentration (NaOH = 9M), a mechanical strength decline of 21% was recorded between a curing time of 7 to 28 days. Moreover, curing at 60°C induced high porosity, significant mass loss and high drying shrinkage. SEM analysis highlighted a dense, homogeneous microstructure without apparent defects, in particular for the samples where the alkali silicate activator was used.
一种用于碱活化材料开发的钢铁工业副产品的增值:固化环境的影响
在自然资源日益稀缺和气候变化加速的背景下,废弃物和副产品的回收和循环利用是应对近几十年来经济和生态约束的有效途径。在土木工程中,工业副产品的增值是一种常见的做法,要么是在波特兰水泥的制造过程中被掺入,要么是在混凝土的生产过程中部分替代水泥。目前的工作旨在开发基于废物的碱活化材料WAAMs,用于土木工程应用,作为水泥基材料的潜在替代品。以炼钢工业副产物——普通粒状高炉渣GBFS为原料,单独作为固体富cao前驱体;分别使用硅酸钠(Na2SiO3)和氢氧化钠(NaOH)两种碱性活化剂制备双组分碱活性材料。除了对硬化样品的微观结构进行分析外,还评估了活化剂/前驱体质量比、NaOH摩尔浓度和两种固化环境(室温和60℃)对试样抗压强度、可水孔隙率、质量损失和干燥收缩率的影响。结果表明:高液固比导致试样的抗压强度降低,而高NaOH摩尔浓度通过降低试样的孔隙率显著改善试样的力学性能。此外,碱性硅酸盐活化剂比碱性氢氧化物活化剂具有更高的抗压强度,特别是当样品在室温下固化时,其最大28天抗压强度达到105.28 MPa。对于使用氢氧化钠溶液活化的样品,结果表明,在60°C下的养护促进了其获得较高的初始抗压强度(7天),随后随着养护时间的延长而降低。作为一个指标,在高碱性浓度(NaOH = 9M)下,固化时间为7至28天,机械强度下降21%。此外,在60°C下固化会导致高孔隙率,显著的质量损失和高干燥收缩率。SEM分析强调了致密,均匀的微观结构,没有明显的缺陷,特别是对于使用碱硅酸盐活化剂的样品。
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来源期刊
Advances in Materials Science
Advances in Materials Science MATERIALS SCIENCE, MULTIDISCIPLINARY-
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