Effect of acid concentration and curing conditions on microstructure, mechanical and electrical properties of phosphate geopolymers

Mahmoud Farag Zawrah , Moataz Bellah Hassan Ata , Hesham Shouib Abdelrahman
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Abstract

This study focuses on how curing conditions and H3PO4 concentration effect on microstructural changes, physical-properties, compressive strength, and electrical properties of phosphate geopolymers. Firstly, phosphate geopolymers were prepared by metakaolin and H3PO4 (8, 10 and 12 M molar-concentrations). Two series of geopolymers were produced: the first series was cured directly in air, while the second series was activated at 75 °C before being cured in air. The phase composition of was investigated by X-ray diffraction technique, and confirmed by infrared spectroscopy. Apparent porosity, bulk density and water absorption were determined according to Archimedes-principle. Scanning electron microscope was utilized to follow the microstructural changes. The compressive strength and electrical resistivity were also investigated. The results revealed that after geopolymerization some amorphous, semi-crystalline and crystalline phases are formed. For example; amorphous alumino-silicate-phosphate-hydrate phases, aluminum hydrogen phosphate 2AlH3(PO4)2.3H2O and berlinite (AlPO4). Moreover, the variation of curing-conditions and acid-concentration had a significant effect on the geopolymerization process which consequently reflected on all properties. The apparent porosity was decreased while the bulk density and compressive strength were increased with increasing the acid concentration up to 10 M, then reduced at 12 M. The electrical resistivity was increased with increasing the acid concentration. Moreover, the geopolymers activated at 75 °C, showed better properties than that cured directly in air. The sample S4 that prepared by 10 M acid and activated at 75 °C exhibited the best properties among the other geopolymers. Their compressive strength, bulk density and apparent porosity values were 68.7 MPa, 2.15 g/cm3, and 20 % respectively.
酸浓度和固化条件对磷酸盐地聚合物微观结构、力学和电性能的影响
研究了固化条件和H3PO4浓度对磷酸盐地聚合物微观结构变化、物理性能、抗压强度和电性能的影响。首先,用偏高岭土和H3PO4(8、10和12 M摩尔浓度)制备磷酸盐地聚合物。生产了两个系列的地聚合物:第一个系列在空气中直接固化,第二个系列在75℃活化后在空气中固化。用x射线衍射技术研究了样品的相组成,并用红外光谱对其进行了表征。根据阿基米德原理测定表观孔隙率、容重和吸水率。利用扫描电镜观察其显微组织变化。并对其抗压强度和电阻率进行了研究。结果表明,经地聚合后形成了非晶、半晶和结晶相。例如;非晶态铝-硅酸盐-磷酸盐-水合相、磷酸氢铝2AlH3(PO4)2.3H2O和白沸石(AlPO4)。此外,固化条件和酸浓度的变化对地聚合过程有显著影响,从而反映在所有性能上。当酸浓度达到10 M时,表观孔隙率减小,体积密度和抗压强度增大,在12 M时减小。电阻率随酸浓度的增加而增加。此外,在75℃下活化的地聚合物比直接在空气中固化的地聚合物表现出更好的性能。在75℃活化条件下,以10 M酸为原料制备的样品S4的性能最好。其抗压强度、容重和表观孔隙率分别为68.7 MPa、2.15 g/cm3和20 %。
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