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Alteration Of Non-swelling Clay Minerals And Magadiite By Acid Activation

机译:酸活化改变非膨胀黏土矿物和辉绿岩

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The bulk material of three kaolins, a sepiolite, an illite and one magadiite were treated with 1, 5 and 10 M H_2SO_4 at 80 ℃ for several hours. The alteration of the non-swelling day mineral structures was controlled by the individual character of each mineral (chemical composition and initial particle size). The reaction resulted in a successive dissolution of the octahedral sheets by edge attack. The number of substitutions by Mg or Fe in the octahedral sheet promoted the dissolution of these layers and the formation of a silica phase. High amounts of Al in the tetrahedral sheet of the clay minerals caused partial dissolution of these sheets. The dissolution of the octahedral cations occurred in the following order: Mg>Fe>Al. Thus, dioctahedral clay minerals were more stable against acid attack than trioctahedral clay minerals. The release of the octahedral cations caused the lightening of the material together with a development of micropores and an increasing specific surface. Dissolution and splitting of the particles required longer reaction times compared to swellable smectites and vermiculites. Acid activation of non-swelling clay minerals can be used to produce layered materials with simple chemical composition and high specific surface area.
机译:将三种高岭土,海泡石,伊利石和一种菱铁矿的块状物料在80℃下分别用1、5和10 M H_2SO_4处理数小时。非膨胀日矿物结构的变化由每种矿物的个体特征(化学组成和初始粒径)控制。该反应导致八面体片材由于边缘侵蚀而连续溶解。八面体片中Mg或Fe的取代数目促进了这些层的溶解和二氧化硅相的形成。粘土矿物的四面体薄片中的大量Al导致这些薄片的部分溶解。八面体阳离子的溶解按以下顺序发生:Mg> Fe> Al。因此,二八面体粘土矿物比三八面体粘土矿物对酸侵蚀更稳定。八面体阳离子的释放导致材料的重量减轻以及微孔的发展和比表面积的增加。与溶胀性蒙脱石和ver石相比,颗粒的溶解和分裂需要更长的反应时间。非膨胀粘土矿物的酸活化可用于生产具有简单化学组成和高比表面积的层状材料。

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