Carbonate minerals, weathering process

Under well drained conditions, iron in soil, unless chelated, is insoluble and tends to be concentrated through weathering as the more soluble ions are removed. In poorly drained soils, iron is reduced to the soluble ferrous state and is either removed from the soil or precipitated as sulfide, phosphate, or carbonate minerals. Other processes, such as chelation, are also effective in mobilizing the iron in the soil profile. The bulk of secondary iron in soils is in the oxide forms. 

Sulfate, halide, and carbonate minerals form in mine waste as a result of chemical weathering reactions and as a by-product of mineral processing. The formation of carbonate minerals is of particular interest for its potential in offsetting greenhouse gas emissions associated with mining. We have documented secondary carbonate mineral precipitation at the Mount Keith Nickel Mine (Western Australia) and the... 

Many technical-chemical processes take maximum benefit of similarities with ongoing processes in Nature, with increased purity or reaction speed as the most important differences. The production of carbonates is a typical example of this, and the process of C02 mineralization for carbon capture and storage (CCS) (see Section 14.4) is in fact the accelerated version of what is known as the natural weathering of minerals. This is a combination of the interacting processes of mechanical and chemical weathering, and relevant to the current discussions are the chemical weathering processes of dissolution and hydrolysis that involve C02 [6, 7]. A dissolution equilibrium reaction that proceeds in Nature with dissolved C02 in water and calcite gives a bicarbonate solution ... 

This process consumes oxygen and produces C02. As a result, the oxygen content of air in soil may be as low as 15%, and the carbon dioxide content may be several percent. Thus, the decay of organic matter in soil increases the equilibrium level of dissolved C02 in groundwater. This lowers the pH and contributes to weathering of carbonate minerals, particularly calcium carbonate. 

To begin the discussion, we will present briefly a view of the modern carbon cycle, with emphasis on processes, fluxes, reservoirs, and the "CO2 problem". In Chapter 4 we introduced this "problem" here it is developed further. We will then investigate the rock cycle and the sedimentary cycles of those elements most intimately involved with carbon. Weathering processes and source minerals, basalt-seawater reactions, and present-day sinks and oceanic balances of Ca, Mg, and C will be emphasized. The modern cycles of organic carbon, phosphorus, nitrogen, sulfur, and strontium are presented, and in Chapter 10 linked to those of Ca, Mg, and inorganic C. In conclusion in Chapter 10, aspects of the historical geochemistry of the carbon cycle are discussed, and tied to the evolution of Earth s surface environment. 

Acid Hydrolysis. The water that enters soil as rain or snow is in equilibrium with CO2 in the atmosphere, which dissolves to form carbonic acid. Unpolluted rainwater has a pH of approximately 5.7, whereas water in soil pores may be exposed to air containing a higher partial pressure of CO2 than the free atmosphere, and hence soil water may be more acidic (see Section 5.4). It is the attack on soil minerals by this weak carbonic acid that is the major chemical weathering process in most soils. For example, acid hydrolysis of calcium carbonate yields calcium and bicarbonate ions ... 

Al3+). In nature they occur widely in silicate minerals, although weathering processes give rise to concentrated deposits of other compounds such as halides (e.g. NaCl, CaF2) carbonates (CaC03) and... 

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