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Synthesis of Nanoscale CaO-Al2O3-SiO2-H2O and Na2O-Al2O3-SiO2-H2O Using the Hydrothermal Method and Their Characterization

机译:水热法合成纳米CaO-Al2O3-SiO2-H2O和Na2O-Al2O3-SiO2-H2O及其表征

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摘要

C-A-S-H (CaO-Al2O3-SiO2-H2O) and N-A-S-H (Na2O-Al2O3-SiO2-H2O) have a wide range of chemical compositions and structures and are difficult to separate from alkali-activated materials. Therefore, it is difficult to analyze their microscopic properties directly. This paper reports research on the synthesis of C-A-S-H and N-A-S-H particles with an average particle size smaller than 300 nm by applying the hydrothermal method. The composition and microstructure of the products with different CaO(Na2O)/SiO2 ratios and curing conditions were characterized using XRD, the RIR method, FTIR, SEM, TEM, and laser particle size analysis. The results showed that the C-A-S-H system products with a low CaO/SiO2 ratio were mainly amorphous C-A-S-H gels. With an increase in the CaO/SiO2 ratio, an excess of Ca(OH)2 was observed at room temperature, while in a high-temperature reaction system, katoite, C4AcH11, and other crystallized products were observed. The katoite content was related to the curing temperature and the content of Ca(OH)2 and it tended to form at a high-temperature and high-calcium environment, and an increase in the temperature renders the C-A-S-H gels more compact. The main products of the N-A-S-H system at room temperature were amorphous N-A-S-H gels and a small amount of sodalite. An increase in the curing temperature promoted the formation of the crystalline products faujasite and zeolite-P. The crystallization products consisted of only zeolite-P in the high-temperature N-A-S-H system and its content were stable above 70%. An increase in the Na2O/SiO2 ratio resulted in more non-bridging oxygen and the TO4 was more isolated in the N-A-S-H structure. The composition and microstructure of the C-A-S-H and N-A-S-H system products synthesized by the hydrothermal method were closely related to the ratio of the raw materials and the curing conditions. The results of this study increase our understanding of the hydration products of alkali-activated materials.
机译:C-A-S-H(CaO-Al2O3-SiO2-H2O)和N-A-S-H(Na2O-Al2O3-SiO2-H2O)具有广泛的化学组成和结构,难以与碱活化材料分离。因此,难以直接分析其微观性质。本文报道了利用水热法合成平均粒径小于300 nm的C-A-S-H和N-A-S-H颗粒的研究。用XRD,RIR法,FTIR,SEM,TEM和激光粒度分析对不同CaO(Na2O)/ SiO2比和固化条件的产物的组成和微观结构进行了表征。结果表明,低CaO / SiO2比的C-A-S-H体系产物主要为非晶C-A-S-H凝胶。随着CaO / SiO2比的增加,在室温下会观察到过量的Ca(OH)2,而在高温反应系统中,会观察到钙钛矿,C4AcH11和其他结晶产物。钙钛矿的含量与固化温度和Ca(OH) 2 的含量有关,并且倾向于在高温和高钙的环境下形成,并且温度的升高使得CASH凝胶更致密。室温下N-A-S-H体系的主要产品是非晶态N-A-S-H凝胶和少量的方钠石。固化温度的升高促进了八面沸石和沸石-P结晶产物的形成。在高温N-A-S-H体系中,结晶产物仅由沸石-P组成,其含量稳定在70%以上。 Na 2 O / SiO 2 比值的增加导致更多的不桥接氧,而TO 4 在NASH结构中的分离度更高。水热法合成的C-A-S-H和N-A-S-H体系产物的组成和微观结构与原料比和固化条件密切相关。这项研究的结果加深​​了我们对碱活化材料水合产物的理解。

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