Calcium carbonate solubility product

Considering pressure, a threshold value is found above which the amount of dissolved C02 and (bi)carbonate, together with the dissolved calcium (determined also by L/S ratio) exceeds the calcium carbonate solubility product, such that precipitation can occur. 

Calculation of Apparent Calcium Carbonate Solubility Products The precise determination of the solubility of calcite... 

Equilibrium with precipitation. The previous example calculated carbonate speciation admitting unrestricted solubility of all species. Actually, it is easily verified that the calculated calcium and carbonate concentrations exceed calcium carbonate solubility as measured by the solubility product... 

I art of the North Branch of the Potomac River runs crystal clear through the scenic Appalachian Mountains but it is lifeless—a victim of acid drainage from abandoned coal mines. As the river passes a paper mill and wastewater treatment plant near Westernport, Maryland, the pH rises from a lethal value of 4.5 to a neutral value of 7.2, at which fish and plants thrive. This fortunate accident comes about when calcium carbonate by-product from papermaking exits the paper mill and reacts with massive quantities of carbon dioxide from bacterial respiration at the sewage treatment plant The resulting soluble bicarbonate neutralizes the acidic river and restores life downstream of the plant In the absence of CO2, solid CaCOj would be trapped at the treatment plant and would never enter the river. 

On archaeological glass objects, layers of reaction products are formed and the main constituents of these cmsts are the less-soluble compounds such as siHca and calcium carbonate, which becomes calcium sulfate. 

Calcium carbonate has normal pH and inverse temperature solubilities. Hence, such deposits readily form as pH and water temperature rise. Copper carbonate can form beneath deposit accumulations, producing a friable bluish-white corrosion product (Fig. 4.17). Beneath the carbonate, sparkling, ruby-red cuprous oxide crystals will often be found on copper alloys (Fig. 4.18). The cuprous oxide is friable, as these crystals are small and do not readily cling to one another or other surfaces (Fig. 4.19). If chloride concentrations are high, a white copper chloride corrosion product may be present beneath the cuprous oxide layer. However, experience shows that copper chloride accumulation is usually slight relative to other corrosion product masses in most natural waters. 

The solubility of calcium carbonate is such that in a saturated solution the product of ion concentrations [Ca+2][C0 2] is 5 X I0 B. Though this may seem quite small, it is large enough to be important to man, especially if he lives in a region of the earth where there are extensive limestone deposits. Calcium carbonate can be dissolved in water, especially if it contains much dissolved C02. This is objectionable because soap added to water which contains even traces of Ca+2 forms a precipitate of calcium stearate. This is the ring that is so difficult to remove from the bathtub. 

NOTE The calcium carbonate limit that RO system designers typically require is +1.6 to 1.8 LSI in the concentrate or reject water, and the calcium sulfate design limit typically calls for a maximum reject water saturation ratio of 1.6 to 1.8 times solubility product. 

The product, calcium hydroxide, is commonly known as slaked lime because, as calcium hydroxide, the thirst of lime for water has been quenched (slaked). Slaked lime is the form in which lime is normally sold because quicklime can set fire to moist wood and paper. In fact, the wooden boats that were once used to transport quicklime sometimes caught fire in the heat of reaction when water seeped into their holds. An aqueous solution of calcium hydroxide, which is slightly soluble in water, is called lime water. It is used as a test for carbon dioxide, with which it reacts to form a suspension of the much less soluble calcium carbonate ... 

The insolubility of calcium carbonate is clearly evident from the value of the solubility product, Ksp, in water at 25°C Ksp = 8.7 x 10-9. The carbonate ions are produced in seawater by the dissociation of carbonic acid that forms from the... 

If S moles of CaCC>3 dissolve in a liter of water, then S moles each of calcium ion and carbonate ion form. With these ion concentrations equal to S, the solubility of CaCC>3 is calculated as 9.3 x 10 5 M. The higher solubility of magnesium carbonate in water, 6.3 x 10 3 M, results from the larger solubility product constant. Nevertheless, both of these carbonate salts are rather insoluble, and the excess carbonate anions provided by the sodium carbonate effectively precipitate the calcium and magnesium ions from solution. 

The use of barium sulphide as a secondary sulphidizer [4] was examined on oxidized lead ores from Sicily (BaS). The results obtained were encouraging. Sulphidization using Na2S can also be improved with the use of ammonium salts (chloride and sulphate). These reagents are used in cases where the ore contains clay minerals and calcium carbonate, which prevents suphidization due to the production of soluble calcium bicarbonate. The ammonium increases the solubility of calcium carbonate and improves sulphidization. 

Let us add the moles of precipitated calcium carbonate as a sixth variable x6, modify the calcium and carbonate conservation equations f2(x) and /3(x) in order to account for solid phase contribution, and use the expression of the solubility product as a sixth equation. The six equations to be solved read... 

Marine chemists measme ion concentrations rather than activities, so the solubility product fiar calcium carbonate is usually defined as... 

CALCIUM/CALMODULIN-DEPENDENT PROTEIN KINASE Calcium carbonate (CaCOs), BIOMINERALIZATION SOLUBILITY PRODUCT Calcium hydroxide (Ca(OH)2),... 

The hrst production step involves recovery of the metal from spodumene. The naturahy occurring ore, alpha-spodumene is heated in a brick-lined rotary kiln at a temperature between 1,075 to 1,100°C. This converts the alpha form to a more reactive form, beta-spodumene. The beta form is heated in a rotary kiln at 250°C with an excess of 93% sulfuric acid. The metal reacts with acid forming hthium sulfate. The kiln discharge is leached with water to separate water-soluble hthium sulfate from several impurity metals. Aqueous solution containing excess sulfuric acid is then neutrahzed by treatment with an excess of ground calcium carbonate (limestone). The solution is fdtered to... 

Magnesium hydroxide is commonly produced from seawater, which is rich in Mg2+ ion. The average concentration of Mg2+ in seawater is about 1,300 mg/L. The first step of the process involves removal of interfering substances from seawater, the most notable being the water-soluble calcium bicarbonate. Bicarbonate removal is crucial, as it can form insoluble calcium carbonate, a side product that cannot be separated from magnesium hydroxide readily. Acidification of seawater converts bicarbonate into carbon dioxide, which is degassed by heating. Alternatively, seawater is treated with bme to convert calcium bicarbonate to carbonate ... 

The stabilizing effect of buffers that have multiple charged species in solution should also be investigated to determine the potential reaction between excipients and API. For example, buffers that use carbonates, citrate, tartrate, and various phosphate salts may precipitate with calcium ions by forming sparingly soluble salts. However, this precipitation is dependent upon the solution pH. Because phosphate can exist in mono-, di-, and tribasic forms, each calcium salt has its own solubility product, and precipitation will only occur when one of the solubility product is exceeded. Calcium ions may also interact or chelate with various amino acids, and other excipients, which may also lower the effective concentration of calcium that is capable of interacting with phosphate ions. Finally, the activity of phosphate ions may be lowered due to interactions with other solution components. 

Dissolution of Sparingly Soluble Salts. Obtain precipitates of calcium carbonate and calcium oxalate in test tubes by reacting the relevant salts. Decant the solutions and pour an acetic acid solution onto the moist precipitates. What happens Repeat the experiment, but use hydrochloric acid instead of the acetic acid. Write the equations of the chemical reactions in the molecular and net ionic forms. Explain the results obtained on the basis of the dissociation constants of the acids and the solubility product. 

Application 1.—The solubility of calcium carbonate at 180 is 14 mg. per liter. The solubility product of the salt is therefore very small (calculate this). 

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