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PETROGRAPHIC RELATIONS IN SOME TYPICAL BAUXITE AND DIASPORE DEPOSITS

机译:一些典型的铝土矿和辉绿岩矿床的岩石学关系

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摘要

Three processes that operate in the formation of bauxite and diaspore deposits are (1) desilication, in which silica is removed from clays, from feldspars, and from other aluminous minerals; (2) migration, in which clay minerals and hydrous aluminum oxides are transported within the deposit from the place where they were formed to their present position; (3) resilication, in which silica is added to gibbsite to form a hydrous aluminum silicate or clay. The desilication of feldspars and parent rocks is usually a two-stage process in which clay minerals such as kaolinite, halloysite, and nontronite are formed first and then silica is removed from them to form gibbsite, boehmite, and diaspore. In the desilication of sedimentary clays, the original structure and texture of the clay are preserved. The formation of bauxite directly from feldspars and nepheline, which has been reported at some localities, does not appear to be the dominant process at the deposits studied during this investigation. Replacement of the clay minerals by gibbsite, boehmite, and diaspore is gradual and involves decrease in silica and increase in alumina, titania, and porosity. Transitional zones of clay-retaining structures of the parent rocks indicate that clay was an intermediate stage in the formation of many bauxite deposits. Desilication takes place in a warm moist climate through the agency of carbonic acid, alkaline carbonates, and magnesium bicarbonate solutions, either as surface weathering or by ground water diffusing through masses of clay of varying permeability and porosity. Clay minerals and hydrous aluminum oxides migrate along cracks and open spaces in the days and bauxite. Pipes and nodules of gibbsite lacking the structure of the parent rock are formed by migration, concentration, and crystallization of secondary gibbsite. The occurrence of cellular kaolin with a structure interpreted as inherited from gibbsite is considered evidence of resilication of gibbsite to kaolin in the bauxite district of Georgia. Dense opaque white to gray kaolinite and some of the "chimney rock" of Georgia may have formed by resilication, which takes place under conditions of poor drainage in low-lying areas. The diaspore of Missouri, Pennsylvania, and Washington and the boehmite of Missouri, Kentucky, Washington, and California were formed from flint clays composed of finely divided kaolinite having low plasticity and breaking with a conchoidal fracture. The gibbsite of the bauxite deposits of Georgia and Alabama was formed from a kaolinitic clay of the hard or semihard type. The chief difference between the flint clays and the hard types of Georgia and Alabama is that the very fine particles of flint clay lack the degrees of symmetry in the stacking of the molecular sheets of kaolinite. The low plasticity of flint clays permitted the retention of openings and cracks without collapse, and this aided their alteration. Possible controlling conditions for the formation of gibbsite, boehmite, and diaspore include temperature, nature of the chemical systems, time, pressure, and drainage.
机译:形成铝土矿和 渗铝沉积物的三个过程是(1)脱硅作用,其中从粘土,长石和其他含铝矿物中去除了 二氧化硅; < sup> (2)迁移,其中粘土矿物质和含水氧化铝 从矿床 形成的位置运到矿床中; (3)硅化作用,是将二氧化硅添加到三水铝石中以形成含水铝硅酸盐或粘土。 长石和母岩的硅化作用为通常是一个 两阶段过程,首先形成粘土矿物,例如高岭石, 硅藻土和绿脱石,然后从其中除去二氧化硅 在沉积粘土的脱水过程中,保留了粘土的原始结构 和质地。在某些地方据报道 直接由长石和霞石形成铝土矿 似乎不是矿床的主要过程 。在调查期间进行了研究。用三水铝石,勃姆石和水硬石替代粘土矿物是逐步的,涉及减少二氧化硅和增加氧化铝,增加二氧化钛和孔隙度。母岩保留粘土的 结构的过渡带表明,粘土是许多铝土矿沉积形成的中间阶段。脱硅 在温暖潮湿的气候中通过碳 酸,碱性碳酸盐和碳酸氢镁溶液( )的作用而发生,无论是表面风化还是表面地下水通过渗透性和孔隙率变化的粘土扩散。 粘土矿物和含水氧化铝在几天和几天内沿着裂缝 和开放空间迁移。铝土矿。缺乏母岩结构的 斜长石的管和结核是通过次生 斜长石的迁移,浓缩和结晶形成的。 / sup>格鲁吉亚铝土矿地区发生的具有被解释为gibbsite的结构的 的细胞高岭土的发生被认为是gbbsite与高岭土发生再结合的证据。致密的白色至灰色高岭石致密 和格鲁吉亚的某些“烟囱岩” 可能是由于弹性作用而形成的,这种情况在恶劣的条件下发生 密苏里州,宾夕法尼亚州和华盛顿州的渗水岩以及密苏里州,肯塔基州,华盛顿州和加利福尼亚州的 勃姆石分别为 由细碎的高岭石 组成的火石粘土形成,具有低可塑性,并具有贝壳状断裂。 乔治亚州和阿拉巴马州的铝土矿床的菱铁矿 由硬或半硬类型的高岭土形成。 the石粘土与佐治亚州和阿拉巴马州的硬类型 的主要区别是非常细的fine石颗粒 粘土在高岭石的分子 薄片的堆叠中缺乏对称度。火石粘土的低可塑性允许 保留开口和裂缝而不会塌陷,这 有助于它们的改变。 三水铝石,勃姆石和水硬岩形成的可能控制条件包括温度,化学系统的性质,时间,压力和排水。

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  • 来源
    《GSA Bulletin》 |1952年第7期|p.649-688|共40页
  • 作者

    VICTOR T ALLEN;

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