Chlorite clay minerals

KIMBARA (K.) and SUDO (C.T.), 1973. Chloritic clay minerals in tuffaceous... 

MARTIN VIVALDI (J.L.) and MACEWAN (D.M.C.), 1960. Corrensite and swelling chlorite. Clay Miner. Bull., 4, 173-81. 

Ball, D.F., 1966. Chlorite clay minerals in Ordovician pumice-tuff and derived soils in Snowdonia, north Wales. Clay Miner., 6 195-209. 

Peterson, N.M.A., 1961. Expandable chloritic clay minerals from Upper Mississippian carbonate rocks, of the Cumberland Plateau in Tennessee. Am. Mineralogist, 46 1245- 1269. 

Leipe, T.,, Gingele, F. X., 2003. The kaoUnite/chlorite clay mineral ratio in surface sediments of the southern Baltic Sea as an indicator for long distance transport of fine-grained material. Baltica, 16, 31-37. 

Micas, chlorites, clay minerals Carbonates, oxides, sulfides, halides Olivines... 

Alkali-carbonate reaction. The alkali-carbonate reaction is different from the alkali-silica reaction in forming different products. Expansive dolomite contains more calcium carbonate than the ideal 50 % (mol) proportion and frequently also contains illite and chlorite clay minerals. 

Stephen, I., and D. M. C. MacEwan, 1951. Some chloritic clay minerals of unusual type. Clay Min. Bull. 1 157. 

In the production of ceramic ware the shape of the ware must be retained after drying and the ware must be free from cracks and other defects. Controlled drying helps to minimize defects. In general, clays containing moderate amounts of nonclay minerals are easier to dry than those composed whoUy of clay minerals. Furthermore, clays composed of iUite, chlorite, and kaolinite are relatively easier to dry than those composed of montmorillonite. 

Main gangue minerals of the Se-type deposits comprise quartz, adularia, illite/ smectite interstratified mixed layer clay mineral, chlorite/smectite interstratified mixed layer clay mineral, smectite, calcite, Mn-carbonates, manganoan caleite, rhodoehrosite, Mn-silicates (inesite, johannsenite) and Ca-silicates (xonotlite, truscottite). 

Principal gangue minerals in base-metal vein-type deposits are quartz, chlorite, Mn-carbonates, calcite, siderite and sericite (Shikazono, 1985b). Barite is sometimes found. K-feldspar, Mn-silicates, interstratified mixed layer clay minerals (chlorite/smectite, sericite/smectite) are absent. Vuggy, comb, cockade, banding and brecciated textures are commonly observed in these veins. 

Zeolite minerals (wairakite, laumontite etc.), mixed-layer clay minerals and sme-cite occur in the upper part of the propylitically altered rocks (e.g., Seigoshi, Fuke, Kushikino), but they are sometimes poor in amounts. Generally carbonates are more abundant in the mine area as in the Toyoha district. Temporal relationship between the formation of high temperature propylitic alteration minerals (epidote, actinolite, prehnite) and low temperature propylitic alteration minerals) (wairakite, laumontite, chlorite/smectite, smectite) in these areas (Seigoshi, Fuke, Kushikino) is uncertain. 

Seigoshi argentite electrum, pearceite, polybasite, pyrargyrite, stephanite, chalcopyrite, fahore, galena, sphalerite quartz, adularia, inesite, xonotlite, chlorite, mixed layer clay mineral, sericite. calcite, rhodochrosite... 

In the Se-type gangue minerals comprise quartz, adularia, illite/smectite inter-stratified mixed layer clay mineral, smectite, calcite, Mn carbonates (manganoan calcite, rhodochrosite), Mn silicates (inesite, johansenite) and Ca silicates (xonotlite, truscottite). In comparison, the Te-type contains fine-grained, chalcedonic quartz, sericite, barite, adularia and chlorite/smectite interstratified mixed layer clay mineral. Carbonates and Mn minerals are very poor in the Te-type and they do not coexist with Te minerals. Carbonates are abundant and barite is absent in the Se-type. Grain size of quartz in the Te-type is very fine, while large quartz crystals are common in the Se-type. 

Izawa et al. (1990) recognized the following alteration zones from the vein towards margin of the Hishikari Au-Ag mine area, chlorite-sericite zone (zone IV), interstratified clay mineral zone (zone III), quartz-smectite zone (zone II) and cristobalite-smectite zone (zone I) and least altered zone (L.A. (least altered) zone) (Fig. 1.131). 

Stoesell, R.K. (1984) Regular solution site-mixing model for chlorites. Clays Clay Minerals, 32, 205-212. 

The dominant alteration minerals at the deeper part of the well include anhydrite, epidote, sericite, chlorite, calcite, dolomite, rhodochrosite, kutnahorite, zeolites (mordenite, clinoptilorite), chlorite and sericite/smectite interstratified clay mineral with subordinate amounts of kaolinite in the shallower part (Imai et al., 1996). 

Figure 6. Scanning electron microscope photos of the troublesome clay minerals kaolinite, chlorite, smectite, and illite. (Reproduced with permission, Halliburton Services.) Continued on next page.

Some of the clays that enter the ocean are transported by river input, but the vast majority of the riverine particles are too large to travel fer and, hence, settle to the seafloor close to their point of entry on the continental margins. The most abundant clay minerals are illite, kaolinite, montmorillonite, and chlorite. Their formation, geographic source distribution and fete in the oceans is the subject of Chapter 14. In general, these minerals tend to undergo little alteration until they are deeply buried in the sediments and subject to metagenesis. 

The CEC of clay minerals is partly the result of adsorption in the interlayer space between repeating layer units. This effect is greatest in the three-layer clays. In the case of montmorillonite, the interlayer space can expand to accommodate a variety of cations and water. This causes montmorillonite to have a very high CEC and to swell when wetted. This process is reversible the removal of the water molecules causes these clays to contract. In illite, some exchangeable potassium is present in the interlayer space. Because the interlayer potassium ions are rather tightly held, the CEC of this illite is similar to that of kaolinite, which has no interlayer space. Chlorite s CEC is similar to that of kaolinite and illite because the brucite layer restricts adsorption between the three-layer sandwiches. 

Rivers transport clay minerals primarily as part of their suspended load (silts and clays). The silt-size fraction is composed of quartz, feldspars, carbonates, and polycrystalline rocks. The clay-sized fraction is dominated by the clay minerals illite, kaolinite, chlorite, and montmorillonite. In addition to suspended particles, rivers carry as a bed load larger size fractions. The bed load constitutes only 10% of the total river load of particles and is predominantly quartz and feldspar sands. 

Ice rafting is responsible for 7% of the terrigenous input of siliclastic particles to the ocean. When the ice melts, the particles settle to the seafloor to form glacial marine deposits. These are currently forming at latitudes greater than 40°N and 50° S. Most of the glacial marine sediments are poorly sorted deposits composed of relatively unweathered materials with chlorite being the dominant clay mineral. In the North Atlantic, layers... 

This information is reported as the percentage that each of the clay mineral type contributes to total identifiable clay mineral content of the noncarbonate clay-sized fraction of the surface sediments. These percentages were determined by x-ray diffraction, which is luiable to identify noncrystalline solids. Using this technique, clay minerals were found to comprise about 60% of the mass of carbonate-free fine-grained fraction. Most of the noncrystalline soUds are probably mixed-layer clay minerals. Carbonate was removed to facilitate the x-ray diffraction characterization of the clay minerals. In some cases, roimd off errors cause the sum of the percentages of kaolinite, illite, montmorillonite, and chlorite to deviate slightly from 100%. 

During this zone refining, the primary (igneous) rocks are transformed into secondary minerals. These include (1) clay minerals, such as phillipsite, chlorite, montmo-rillonite (smectite), saponite, celadonite, and zeolite (2) iron oxyhydroxides (3) pyrite (4) various carbonates and (5) quartz. These minerals form rapidly, within 0.015 and 0.12 million years after creation of the oceanic crust at the MOR. During these alteration... 

The dominant clay mineral at high latitudes is chlorite. In addition to ice rafting, lithogenous materials are transported in the polar oceans by rivers and winds. Polar seas are also characterized by diatomaceous oozes due to the occurrence of upwelling supported by divergence at 60°N and 60°S. 

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