Primary mineral

Soil minerals are classified as primary and secondary. Primary minerals are formed under igneous conditions and found in volcanic and similar rocks. Many of them strictly are not thermodynamically stable (or the most stable) under surface conditions thus they evolve slowly in the presence of water toward more stable structures, which are the secondary minerals. However, some primary minerals (such as quartz and micas) do remain stable and are found intermixed with secondary ones. 

FIGURE 7.4 Abundance of the most important elements in soils (black bars) and in the earth s crust (grey bars) in (a) mass units (logarithm of concentration, in parts per million) and (h) molar units (logarithm of concentration in millimoles per kilogram). 

The silica tetrahedra can be linked in a number of ways to form silicates of differing structures, and hence susceptibility to weathering 

In Table 3, susceptibility to weathering increases down the list as fewer silicon-oxygen bonds need to be broken to release silicate. Consequently, quartz and feldspars especially, but also mica in temperate soils, are common inherited minerals in the coarse particle size fractions of soil (the silt and sand fractions, 0.002-2 mm). The amphiboles, pyroxenes, and olivine are much more easily weathered. Thus, soils derived from parent material with rock containing a predominance of framework silicates e.g. granite, sandstone) tend to be more sandy, while those derived from rocks containing the more easily weathered minerals tend to be more clayey. 

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Muscovite mica formed as a primary mineral in pegmatites and granodiorite differs in physical properties compared to muscovite mica formed by secondary alteration (mica schist) (Table 2). The main differences are in flexibiUty and abiUty to be delaminated. Primary muscovite is not as brittle and delaminates much easier than muscovite formed as a secondary mineral. Mineralogical properties of the principal natural micas are shown in Table 3. The make-up of muscovite, phlogopite, and biotite are as follows ... 

Phosphorus [7723-14-0] is a nonmetaUic element having widespread occurrence in nature as phosphate compounds (see Phosphoric acid and phosphates). Fluorapatite [1306-03-4], Ca F(P0 2> is the primary mineral in phosphate rock ores from which useful phosphoms compounds (qv) ate produced. The recovery from the ore into commercial chemicals is accompHshed by two routes the electric furnace process, which yields elemental phosphoms and the wet acid process, which generates phosphoric acid. The former is discussed herein (see Furnaces, electric). Less than 10% of the phosphate rock mined in the world is processed in electric furnaces. Over 90% is processed by the wet process, used primarily to make fertilisers (qv). 

There are over 65 known vanadium-bearing minerals, some of the more important are Hsted in Table 1. Patronite, bravoite, sulvanite, davidite, and roscoehte are classified as primary minerals, whereas all of the others are secondary products which form in the oxidizing zone of the upper Hthosphere. 

During chemical weathering, rocks and primary minerals become transformed to solutes and sods, and eventually to sediments and sedimentary... 

Copper ore minerals maybe classified as primary, secondary, oxidized, and native copper. Primaryrninerals were concentrated in ore bodies by hydrothermal processes secondary minerals formed when copper sulfide deposits exposed at the surface were leached by weathering and groundwater, and the copper reprecipitated near the water table (see Metallurgy, extractive). The important copper minerals are Hsted in Table 1. Of the sulfide ores, bornite, chalcopyrite, and tetrahedrite—teimantite are primary minerals and coveUite, chalcocite, and digenite are more commonly secondary minerals. The oxide minerals, such as chrysocoUa, malachite, and azurite, were formed by oxidation of surface sulfides. Native copper is usually found in the oxidized zone. However, the principal native copper deposits in Michigan are considered primary (5). 

The inorganic component of soil is dominated by four elements O, Si, Al, and Fe (Jackson, 1964). Together with Mg, Ca, Na, and K they constitute 99% of the soil mineral matter (see Table 8-2). Minerals in soil are divided into primary and secondary minerals. Primary minerals, which occur in igneous, metamorphic, and sedimentary rocks, are inherited by soil... 

Secondary minerals. As weathering of primary minerals proceeds, ions are released into solution, and new minerals are formed. These new minerals, called secondary minerals, include layer silicate clay minerals, carbonates, phosphates, sulfates and sulfides, different hydroxides and oxyhydroxides of Al, Fe, Mn, Ti, and Si, and non-crystalline minerals such as allophane and imogolite. Secondary minerals, such as the clay minerals, may have a specific surface area in the range of 20-800 m /g and up to 1000 m /g in the case of imogolite (Wada, 1985). Surface area is very important because most chemical reactions in soil are surface reactions occurring at the interface of solids and the soil solution. Layer-silicate clays, oxides, and carbonates are the most widespread secondary minerals. 

Once a layer-silicate clay forms, it does not necessarily remain in the soil forever. As conditions change it too may weather and a new mineral may form that is more in equilibrium with the new conditions. For example, it is common in young soils for the concentrations of cations such as K, Ca, or Mg in the soil solution to be high, but as primary minerals are weathered and disappear, cation concentrations will decrease. With a decrease in solution cations, a layer-silicate such as vermiculite will no longer be stable and can weather. In its place. 

Contributions made by physical weathering are much greater in steep terrains (i.e., more primary minerals remain), and overall weathering rates are higher. 

The most stable minerals are often physically eroded before they have a chance to chemically decompose. Minerals that decompose contribute to the dissolved load in rivers, and their solid chemical-weathering products contribute to the secondary minerals in the solid load. The secondary minerals and the more stable primary minerals are the most important constituents of clastic sedimentary rocks. Consequently, the secondary minerals of one cycle of erosion are... 

When soil thickness is at the stable value (F), erosion is transport limited. Chemical weathering is also transport limited. This is, however, not because of reaction kinetics instead this limitation is primarily controlled by physical factors, most probably, restricted access of water to the primary minerals. 

The waste organic acids dissolved carbonate minerals, alumino-silicate minerals, and iron/manganese-oxide coatings on the primary minerals in the injection zone. 

Smectite is the first secondary mineral to form upon rock weathering in the semi-arid to sub-humid tropics. Smectite clay retains most of the ions, notably Ca2+ and Mg2+, released from weathering primary silicates. Iron, present as Fe2+ in primary minerals, is preserved in the smectite crystal lattice as Fe3+. The smectites become unstable as weathering proceeds and basic cations and silica are removed by leaching. Fe3+-compounds however remain in the soil, lending it a reddish color aluminum is retained in kaolinite and A1-oxides. Leached soil components accumulate at poorly drained, lower terrain positions where they precipitate and form new smectitic clays that remain stable as long as the pH is above neutral. Additional circumstances for the dominance of clays are ... 

Shindo H, Huang PM (1985b) Catalytic polymerization of hydroquinone by primary minerals. Soil Sci 139 505-511... 

The processes described and their kinetics is of importance in the accumulation of trace metals by calcite in sediments and lakes (Delaney and Boyle, 1987) but also of relevance in the transport and retention of trace metals in calcareous aquifers. Fuller and Davis (1987) investigated the sorption by calcareous aquifer sand they found that after 24 hours the rate of Cd2+ sorption was constant and controlled by the rate of surface precipitation. Clean grains of primary minerals, e.g., quartz and alumino silicates, sorbed less Cd2+ than grains which had surface patches of secondary minerals, e.g., carbonates, iron and manganese oxides. Fig. 6.11 gives data (time sequence) on electron spin resonance spectra of Mn2+ on FeC03(s). 

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