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Kaolinite origin

Original kaolinite Sodium kaolinite Ammonium kaolinite Hydrogen kaolinite Original montmorillonite Sodium montmorillonite Ammonium montmorillonite Hydrogen montmorillonite... [Pg.170]

Ash is the inorganic residue that remains after the coal has been burned under specified conditions, and it is composed largely of compounds of sihcon, aluminum, iron, and calcium, and minor amounts of compounds of magnesium, sodium, potassium, phosphorous, sulfur, and titanium. Ash may vaiy considerably from the original mineral matter, which is largely kaolinite, iUite, montmoriUonite, quartz, pyrites, and gypsum. [Pg.2359]

Ore deposits associated with volcanic rocks generally exhibit polymetallic (Cu, Pb, Zn, Sn, W, Au, Ag, Mo, Bi, Sb, As and In) mineralization. Sulfur isotopic values of sulfides from these deposits are close to 0%o, suggesting a deep-seated origin of the sulfide sulfur. Clay deposits (pyrophyllite, sericite and kaolinite) are associated with both felsic volcanic rocks and ilmenite-series granitic rocks of late Cretaceous age in the San-yo Belt. [Pg.4]

Hydrothermal alteration in the Osorezan area is extensive. At the foot of the lava dome, highly silicified alteration occurs. From this zone towards marginal parts, kaolinite zone and montmorillonite zone exist. This type of alteration was caused by the acid hydrothermal solution. But at present such acid hot solutions are not present in the Osorezan area. The acid solution is considered to be of volcanic origin. It is therefore thought that the water chemistry evolved from extremely acid at the early stage to neutral pH at present (Aoki, 1992a). [Pg.315]

The presence of excess salt, particularly of bivalent inorganics can reduce the electrostatic repulsion between the anionic polymer and the kaolinite particles and enhance flocculation (24,25). The optimum flocculation of fine coal and coal refuse (which contained 13 to 65% clays) obtained by Lewellyn and Wang(24) with hydrolyzed polyacrylamide containing 70% acrylate in fact might have resulted from the use of recycled water which contained 55 ppm Ca and 30 ppm Mg. Other works in literature have reported maximum flocculation of kaolinite to occur with 30% hydrolyzed polyacrylamide (5,6,10,26,27). Such differences in reported results could easily result from variations in water chemistry, originating either with the water used or with dissolved organics released by the mineral itself. [Pg.407]

Polyelectrolytes provide excellent stabilisation of colloidal dispersions when attached to particle surfaces as there is both a steric and electrostatic contribution, i.e. the particles are electrosterically stabilised. In addition the origin of the electrostatic interactions is displaced away from the particle surface and the origin of the van der Waals attraction, reinforcing the stability. Kaolinite stabilised by poly(acrylic acid) is a combination that would be typical of a paper-coating clay system. Acrylic acid or methacrylic acid is often copolymerised into the latex particles used in cement sytems giving particles which swell considerably in water. Figure 3.23 illustrates a viscosity curve for a copoly(styrene-... [Pg.96]

Figure 2. Infrared absorption spectra of the 8.4A hydrate (A), the 8.6A hydrate (B), the 10A hydrate (C)i and the original kaolinite used to synthesize the three hydrates (D). Figure 2. Infrared absorption spectra of the 8.4A hydrate (A), the 8.6A hydrate (B), the 10A hydrate (C)i and the original kaolinite used to synthesize the three hydrates (D).
The size distribution of the kaolinite is quite variable and again the Kingston sample differed in that most of the kaolinite has sodium associated with it and could therefore be considered a smectite rather than kaolinite. Marcasite is commonly present as a replacement of original coal particles. The gypsum is present mainly in the -20 ym size range. Overall the mineral matter content of the lignites is of the order of 5%-10% (i.e. a medium distribution density). [Pg.28]

Fig. 16.9 Electron micrographs of soil lepidocro-cite. a) Large multidomainic lath-like crystal viewed perpendicularto [001] with laminar pores from a re-doximorphic soil, Natal, South Africa, b) Poorly crystalline grassy lepidocrocite crystals mixed with tiny ferrihydrite particles and pseudo-hexagonal kaolinite platelets. Origin as before (a. b courtesy P. Self), c) Small lepidocrocite crystal from a hydromorphic soil (with ferrihydrite) viewed perpendicularto [001] and showing (020) lattice fringes (see also Schwert-mann. Taylor, 1989,with permission). Fig. 16.9 Electron micrographs of soil lepidocro-cite. a) Large multidomainic lath-like crystal viewed perpendicularto [001] with laminar pores from a re-doximorphic soil, Natal, South Africa, b) Poorly crystalline grassy lepidocrocite crystals mixed with tiny ferrihydrite particles and pseudo-hexagonal kaolinite platelets. Origin as before (a. b courtesy P. Self), c) Small lepidocrocite crystal from a hydromorphic soil (with ferrihydrite) viewed perpendicularto [001] and showing (020) lattice fringes (see also Schwert-mann. Taylor, 1989,with permission).
Studies of hydrothermal alteration products associated with ore mineralization in acidic rocks have established the general propensity for the original minerals to be replaced by illite, sericite or hydromica in the innermost zone near the source of hydrothermal fluids and by kaolinite or expandable minerals further from the vein or center of fluid emanation. The newly-formed "mica" can be 2M, 1M, or lMd in polymorph and range compositionally from muscovite to a low potassium, silicic species which can be assimilated in the term illite (Lowell and Guilbert, 1970 Schoen and White, 1966, 1965 Kelly and Kerr, 1957 Bonorino, 1959 Tomita, e al., 1969 Yoder and Eugster, 1955 Meyer and Hemley, 1959, among many authors). [Pg.38]

Distribution coefficients were measured employing batch methods. The solution (ml) to clay (mg) ratios were aporoximate-ly as follows 1 5 attapulgite 1 60 montmorilIonite and 1 25 kaolinite. The solutions were brines (NaCl) buffered with pH 5 acetate solution. The original stock solution contained 3 M NaCl and 1 M Na acetate buffer. The lower [Na] solutions were made by... [Pg.201]

Kaolins. The kaolin minerals include kaolinite. dickite. and nacrite which all have composition AUOi 2 SiO 2 FLO halloysite (7 At. AGO, 2 SiO, 2 H.O and halfoysile (10 A). Al 0, 2 SiO 4 H 0 The struclural formulas for kaolinite and halloysite tIO At. which are shown in Figure I, are AbSiaOiotOH)). and AljSi.iO, i(OH) -4 H,(). respectively. The so-called fire day mineral is a h-axis disordered kaolinite halloysite (7 A) and halloysite (10 A) are disordered along both the a- and h-Mcs Indeed, most variations in the kaolin group originate as structural polymorphs, related to variations in layer slacks. [Pg.387]

Reconstruction of Original Minerals. To test the conclusions of Feth (3) concerning the weathering reaction, allow an average spring water to back-react with kaolinite, the chief weathering product, and see if the original rock minerals can be formed. The reactions and products... [Pg.229]

Next all Mg2+ and enough K HCXV, and Si02 reacted with kaolinite to make biotite, leaving a small residue of Kf, HCCV, and Si02 to form K-feldspar. Some silica remained—about 4% of the original concentration. Thus, the mass balance is probably within the limits of error of the original values of concentration used for the median composition of spring waters. [Pg.231]


See other pages where Kaolinite origin is mentioned: [Pg.195]    [Pg.196]    [Pg.196]    [Pg.311]    [Pg.313]    [Pg.180]    [Pg.334]    [Pg.311]    [Pg.313]    [Pg.45]    [Pg.347]    [Pg.111]    [Pg.5]    [Pg.520]    [Pg.4]    [Pg.586]    [Pg.320]    [Pg.389]    [Pg.427]    [Pg.632]    [Pg.252]    [Pg.84]    [Pg.34]    [Pg.49]    [Pg.714]    [Pg.73]    [Pg.229]    [Pg.872]    [Pg.102]    [Pg.90]    [Pg.94]    [Pg.131]    [Pg.13]    [Pg.137]    [Pg.142]    [Pg.145]    [Pg.46]   
See also in sourсe #XX -- [ Pg.141 , Pg.142 ]




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