Geology topics

Bruce F. Bohor

Publications and source records attributed to Bruce F. Bohor.

6 recordsLinked to original sources

USGS2024

Surface area of montmorillonite from the dynamic sorption of nitrogen and carbon dioxide

Surface area determinations were made on a montmorillonite with various cations emplaced on the exchangeable sites, utilizing nitrogen and carbon dioxide as adsorbates at 77 ° K and 195 ° K, respectively, in a dynamic system. From the fraction of a Mississippi montmorillonite less than about 1 μ in size, samples were prepared by replacing the original exchangeable cations with Li + , Na + , K + , Rb + , Cs + , Mg ++ , Ca ++ , Ba ++ , and NH 4 + , forming a series of homoionic montmorillonite species. Surface areas from 3-point B.E.T. plots (half-hour adsorption points), with nitrogen as the adsorbate, ranged from 61 m 2 /g for Li-montmorillonite to 138 m 2 /g for Cs-montmorillonite, thus reflecting a certain degree of nitrogen penetration between layers. Complete penetration should theoretically result in a surface area of over 300 m 2 /g for this clay with a nitrogen monolayer between each pair of platelets. The experimental data indicate that the extent of penetration is time-dependent and is also a function of the interlayer forces as governed by the size and charge of the replaceable cation. This finding negates the generally accepted concept that nitrogen at 77 ° K does not penetrate the layers and provides a measure only of the external surface of expandable clay minerals. A further measure of the variation of interlayer forces is provided by the adsorption of carbon dioxide at 195 ° K. Surface area values ranged from 99 m 2 /g for Li-montmorillonite to 315 m 2 /g for Csmontmorillonite. Although the carbon dioxide molecule is larger than the nitrogen molecule, its greater penetration apparently is a result of its being kinetically more energetic (with a larger diffusion coefficient) at its higher adsorption temperature. Similar differences have been found with both adsorbates in the study of microporous substances, such as coal, where activated diffusion is of considerable significance.

Clays and Clay Minerals↗

USGS2024

Surface area of vermiculite with nitrogen and carbon dioxide as adsorbates

Surface-area studies were made on several homoionic vermiculites with both nitrogen and carbon dioxide as adsorbates. These studies show that only very slight penetration occurs between individual vermiculite platelets. This is in contrast to an earlier investigation of montmorillonite where it was found that the degree of penetration between layers is quite high, particularly for carbon dioxide, and is governed by the size and charge of the interlayer cation. The inability of these adsorbates to penetrate substantially between vermiculite platelets is due primarily to this mineral's high surface-charge density. The extent of penetration of nitrogen and carbon dioxide at the edges of vermiculite platelets, though slight, is influenced by the coordinated water retained within the sample at a given degassing temperature. Forces between layers are weakened with increasing water content, which permits slightly greater penetration by adsorbate gases. Thus, the surface area of vermiculite, as determined by gas adsorption, is larger than the calculated external surface area based upon particle size and shape considerations. In addition, "extra" surface is provided by the lifting and scrolling of terminal platelets. These morphological features are shown in scanning electron micrographs of a naturally occuring vermiculite.

Clays and Clay Minerals↗

USGS2024

Chemical disaggregation of kaolinitic claystones (tonsteins and flint clays)

The coarse, non-clay fraction of many flint-like kaolinitic claystones often contains mineral grains diagnostic of the claystone's origin and, in the case of tonsteins (altered volcanic ashes), may also provide minerals suitable for radiometric dating. Separation of the non-clay mineral fraction is often difficult because flint clays and flint-like clays resist slaking in water and thus are difficult to disaggregate. Chemical disaggregation of resistant kaolinitic claystones may be achieved by immersion in either hydrazine monohydrate or DMSO for periods ranging from one day to several weeks. Generally, hydrazine monohydrate works more quickly and efficiently than DMSO to disaggregate most kaolinitic claystones and flint clays.

Clays and Clay Minerals↗

USGS2012

The first direct evidence of pre-columbian sources of palygorskite for Maya Blue

Maya Blue, a nano-structured clay–organic complex of palygorskite and indigo, was used predominantly before the Spanish Conquest. It has fascinated chemists, material scientists, archaeologists and art historians for decades because it is resistant to the effect of acids, alkalis, and other reagents, and its rich color has persisted for centuries in the harsh tropical climate of southern Mesoamerica. One of its components, palygorskite, is part of modern Maya indigenous knowledge, and ethnohistoric and archaeological data suggest that its modern sources were probably utilized in Prehispanic times. Yet no direct evidence verifies that palygorskite was actually mined from these sources to make Maya Blue. Here we characterize these sources compositionally, and compare our analyses to those of Maya Blue from Chichén Itzá and Palenque. We demonstrate that the palygorskite in most of these samples came from modern mines, providing the first direct evidence for the use of these sources for making Maya Blue. These findings reveal that modern Maya indigenous knowledge about palygorskite, its mining, and its source locations, is at least seven centuries old.

Journal of Archaeological Science↗

USGS1990

Shock-induced microdeformations in quartz and other mineralogical indications of an impact event at the Cretaceous-Tertiary boundary

The event terminating the Cretaceous period and the Mesozoic era caused massive extinctions of flora and fauna worldwide. Theories of the nature of this event can be classed as endogenic (volcanic, climatic, etc.) or exogenic (extraterrestrial causes). Mineralogical evidence from the boundary clays and claystones strongly favor the impact of an extraterrestrial body as the cause of this event. Nonmarine KT boundary claystones are comprised of two separate layers—an upper layer composed of high-angle ejecta material (shocked quartz, altered glass and spinel) and a basal kaolinitic layer containing spherules, clasts, and altered glass, together with some shocked grains. Recognition of this dual-layered nature of the boundary clay is important for the determination of the timing and processes involved in the impact event and in the assignment and interpretation of geochemical signatures. Multiple sets of shock-induced microdeformations (planar features) in quartz grains separated from K T boundary clays provide compelling evidence of an impact event. This mineralogical manifestation of shock metamorphism is associated worldwide with a large positive anomaly of iridium in these boundary clays, which has also been considered indicative of the impact of a large extraterrestrial body. Global distributions of maximum sizes of shocked quartz grains from the boundary clays and the mineralogy of the ejecta components favor an impact on or near the North American continent. Spinel crystals (magnesioferrite) occur in the boundary clays as micrometer-sized octahedra or skeletal forms. Their composition differs from that of spinels found in terrestrial oceanic basalts. Magnesioferrite crystals are restricted to the high-angle ejecta layer of the boundary clays and their small size and skeletal morphology suggest that they are condensation products of a vaporized bolide. Hollow spherules ranging up to 1 mm in size are ubiquitously associated with the boundary clays. In nonmarine sections, where a high-angle ejecta layer and an underlying kaolinitic layer can be distinguished, the spherules are found only in the kaolinitic layer. The morphologies and surface features of these spherules suggest that they are original forms, and not secondary growths or algal bodies. These impact spherules closely resemble microtektites in size and shape. All of these features of the boundary clay are uniquely associated with impact, and cannot have been formed by volcanic or other terrestrial processes.

Colorado, Montana, New Mexico, Wyoming↗

USGS1987

Shocked quartz in the Cretaceous-Tertiary boundary clays: Evidence for a global distribution

Shocked quartz grains displaying planar features were isolated from Cretaceous- Tertiary boundary clays at five sites in Europe, a core from the north-central Pacific Ocean, and a site in New Zealand. At all of these sites, the planar features in the shocked quartz can be indexed to rational crystallographic planes of the quartz lattice. The grains display streaking indicative of shock in x-ray diffraction photographs and also show reduced refractive indices. These characteristic features of shocked quartz at several sites worldwide confirm that an impact event at the Cretaceous-Tertiary boundary distributed ejecta products in an earth-girdling dust cloud, as postulated by the Alvarez impact hypothesis.

Science↗