通过煅烧增强地聚合物的合成:增加天然材料利用的潜力

IF 2.9 Q1 MATERIALS SCIENCE, CERAMICS
Erhan Albayrak, Sevgi Özen
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引用次数: 0

摘要

本研究以两种煅烧火山灰为原料合成地聚合物。通过抗压强度、XRD、FTIR、SEM/EDX等分析手段研究了土聚合物的力学性能和微观结构。结果表明,斜发沸石基地聚合物在室温下具有足够的强度,无需热固化,这是天然材料基地聚合物的一个关键限制。相比之下,尽管经过煅烧,长石基地聚合物在环境和50°C固化条件下都表现出不充分的活化,未能获得显著的强度增益。这一发现强调了煅烧在材料活化中的关键作用,同时强调了原材料成分对地聚合物整体性能的重大影响。XRD和FTIR分析显示,斜沸石峰强度降低,表明其积极参与地聚合物的形成,而无定形峰的存在表明地聚合物凝胶网络发育良好。SEM/EDX证实了斜发沸石基地聚合物中稳定的Si/Al比,进一步支持了其增强的机械性能。这些发现突出了矿物学表征在预测地聚合物反应性和优化合成条件方面的重要意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Enhancing geopolymer synthesis through calcination: Increasing the potential of natural material utilization
In this study, two types of calcined pozzolan were used as raw materials for geopolymer synthesis. The mechanical and microstructural properties of the geopolymers were investigated through compressive strength, XRD, FTIR and SEM/EDX analyses. Results indicated that the clinoptilolite-based geopolymer developed sufficient strength at room temperature, eliminating the need for thermal curing, a key limitation of natural material-based geopolymers. In contrast, despite calcination, the feldspar-based geopolymer exhibited inadequate activation and failed to achieve significant strength gains under both ambient and 50 °C curing conditions. This finding emphasizes the critical role of calcination in material activation while highlighting the significant impact of raw material composition on the overall performance of geopolymers. XRD and FTIR analyses revealed reduced clinoptilolite peak intensities, indicating its active involvement in geopolymer formation, while the presence of an amorphous hump suggested a well-developed geopolymeric gel network. SEM/EDX confirmed a stable Si/Al ratio in the clinoptilolite-based geopolymer, further supporting its enhanced mechanical performance. These findings highlight the significance of mineralogical characterization in predicting geopolymer reactivity and optimizing synthesis conditions.
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来源期刊
Open Ceramics
Open Ceramics Materials Science-Materials Chemistry
CiteScore
4.20
自引率
0.00%
发文量
102
审稿时长
67 days
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