A Stiff diagram, or Stiff pattern, is a graphical representation of chemical analyses, first developed by H.A. Stiff in 1951. It is widely used by hydrogeologists and geochemists to display the major ion composition of a water sample. A polygonal shape is created from four parallel horizontal axes extending on either side of a vertical zero axis. Cations are plotted in milliequivalents per liter on the left side of the zero axis, one to each horizontal axis, and anions are plotted on the right side. Stiff patterns are useful in making a rapid visual comparison between water from different sources. An alternative to the Stiff diagram is the Maucha diagram.
Stiff diagrams can be used:
A typical Stiff diagram is shown in the figure (right). By standard convention, Stiff diagrams are created by plotting the equivalent concentration of the cations to the left of the center axis and anions to the right. The points are connected to form the figure. When comparing Stiff diagrams between different waters it is important to prepare each diagram using the same ionic species, in the same order, on the same scale.
Environmental laboratories typically report concentrations for anion and cation parameters using units of mass/volume, usually mg/L. In order to convert the mass concentration to an equivalent concentration the following mathematical relationship is used:
For example, a water with a calcium concentration of 120 mg/L would have the following calcium equivalent concentration:
In chemistry, a salt is a chemical compound consisting of an ionic assembly of cations and anions. Salts are composed of related numbers of cations and anions so that the product is electrically neutral. These component ions can be inorganic, such as chloride (Cl−), or organic, such as acetate ; and can be monatomic, such as fluoride (F−) or polyatomic, such as sulfate.
The chloride ion is the anion Cl−. It is formed when the element chlorine gains an electron or when a compound such as hydrogen chloride is dissolved in water or other polar solvents. Chloride salts such as sodium chloride are often very soluble in water. It is an essential electrolyte located in all body fluids responsible for maintaining acid/base balance, transmitting nerve impulses and regulating fluid in and out of cells. Less frequently, the word chloride may also form part of the "common" name of chemical compounds in which one or more chlorine atoms are covalently bonded. For example, methyl chloride, with the standard name chloromethane is an organic compound with a covalent C−Cl bond in which the chlorine is not an anion.
Fluoride is an inorganic, monatomic anion with the chemical formula F−
, whose salts are typically white or colorless. Fluoride salts typically have distinctive bitter tastes, and are odorless. Its salts and minerals are important chemical reagents and industrial chemicals, mainly used in the production of hydrogen fluoride for fluorocarbons. Fluoride is classified as a weak base since it only partially associates in solution, but concentrated fluoride is corrosive and can attack the skin.
Hard water is water that has high mineral content. Hard water is formed when water percolates through deposits of limestone, chalk or gypsum which are largely made up of calcium and magnesium carbonates, bicarbonates and sulfates. Iron oxides or iron carbonates can give a reddish brown colouration to hard water deposits
Hypocalcemia is low calcium levels in the blood serum. The normal range is 2.1–2.6 mmol/L with levels less than 2.1 mmol/l defined as hypocalcemia. Mildly low levels that develop slowly often have no symptoms. Otherwise symptoms may include numbness, muscle spasms, seizures, confusion, or cardiac arrest.
Magnesium chloride is the name for the chemical compound with the formula MgCl2 and its various hydrates MgCl2(H2O)x. Anhydrous MgCl2 contains 25.5% elemental magnesium by mass. These salts are typical ionic halides, being highly soluble in water. The hydrated magnesium chloride can be extracted from brine or sea water. In North America, magnesium chloride is produced primarily from Great Salt Lake brine. It is extracted in a similar process from the Dead Sea in the Jordan Valley. Magnesium chloride, as the natural mineral bischofite, is also extracted (by solution mining) out of ancient seabeds, for example, the Zechstein seabed in northwest Europe. Some magnesium chloride is made from solar evaporation of seawater. Anhydrous magnesium chloride is the principal precursor to magnesium metal, which is produced on a large scale. Hydrated magnesium chloride is the form most readily available.
Calcium fluoride is the inorganic compound of the elements calcium and fluorine with the formula CaF2. It is a white insoluble solid. It occurs as the mineral fluorite (also called fluorspar), which is often deeply coloured owing to impurities.
Dolomite (also known as dolomite rock, dolostone or dolomitic rock) is a sedimentary carbonate rock that contains a high percentage of the mineral dolomite, CaMg(CO3)2. In old USGS publications, it was referred to as magnesian limestone, a term now reserved for magnesium-deficient dolomites or magnesium-rich limestones. Dolomite has a stoichiometric ratio of nearly equal amounts of magnesium and calcium. Most dolomite rock formed as a magnesium replacement of limestone or lime mud before lithification. Dolomite rock is resistant to erosion and can either contain bedded layers or be unbedded. It is less soluble than limestone in weakly acidic groundwater, but it can still develop solution features (karst) over time. Dolomite rock can act as an oil and natural gas reservoir.
Alkalinity is the capacity of water to resist acidification. It should not be confused with basicity which is an absolute measurement on the pH scale.
Ion exchange usually describes a processes of purification of aqueous solutions using solid polymeric ion exchange resin. More precisely, the term encompasses a large variety of processes where ions are exchanged between two electrolytes. Aside from its use to purify drinking water, the technique is widely applied for purification and separation of a variety of industrially and medicinally important chemicals. Although the term usually refers to applications of synthetic (man-made) resins, it can include many other materials such as soil.
In electrochemistry, and more generally in solution chemistry, a Pourbaix diagram, also known as a potential/pH diagram, EH–pH diagram or a pE/pH diagram, is a plot of possible thermodynamically stable phases of an aqueous electrochemical system. Boundaries (50 %/50 %) between the predominant chemical species are represented by lines. As such a Pourbaix diagram can be read much like a standard phase diagram with a different set of axes. Similarly to phase diagrams, they do not allow for reaction rate or kinetic effects. Beside potential and pH, the equilibrium concentrations are also dependent upon, e.g., temperature, pressure, and concentration. Pourbaix diagrams are commonly given at room temperature, atmospheric pressure, and molar concentrations of 10−6 and changing any of these parameters will yield a different diagram.
Carbonate hardness, is a measure of the water hardness caused by the presence of carbonate and bicarbonate anions. Carbonate hardness is usually expressed either in degrees KH (dKH), or in parts per million calcium carbonate. One dKH is equal to 17.848 mg/l (ppm) CaCO
3, e.g. one dKH corresponds to the carbonate and bicarbonate ions found in a solution of approximately 17.848 milligrams of calcium carbonate(CaCO
3) per litre of water. Both measurements are usually expressed as mg/l CaCO
3 – meaning the concentration of carbonate expressed as if calcium carbonate were the sole source of carbonate ions.
Kröger–Vink notation is a set of conventions that are used to describe electric charges and lattice positions of point defect species in crystals. It is primarily used for ionic crystals and is particularly useful for describing various defect reactions. It was proposed by F. A. Kröger and H. J. Vink.
Alkali, or Alkaline, soils are clay soils with high pH, a poor soil structure and a low infiltration capacity. Often they have a hard calcareous layer at 0.5 to 1 metre depth. Alkali soils owe their unfavorable physico-chemical properties mainly to the dominating presence of sodium carbonate, which causes the soil to swell and difficult to clarify/settle. They derive their name from the alkali metal group of elements, to which sodium belongs, and which can induce basicity. Sometimes these soils are also referred to as alkaline sodic soils.
Alkaline soils are basic, but not all basic soils are alkaline.
In 1944, Arthur M. Piper proposed an effective graphic procedure for presenting water chemistry data to help in understanding the sources of the dissolved constituents in water. This procedure is based on the premise that cations and anions in water are generally in chemical equilibrium.
Electrodeionization (EDI) is a water treatment technology that utilizes electricity, ion exchange membranes and resin to deionize water and separate dissolved ions (impurities) from water. It differs from other water purification technologies in that it is done without the use of chemical treatments and is usually a polishing treatment to reverse osmosis (RO). There are also EDI units that are often referred to as continuous electrodeionization (CEDI) since the electric current regenerates the resin mass continuously. CEDI technique can achieve very high purity, with conductivity below 0.1 μS/cm.
A metal ion in aqueous solution or aqua ion is a cation, dissolved in water, of chemical formula [M(H2O)n]z+. The solvation number, n, determined by a variety of experimental methods is 4 for Li+ and Be2+ and 6 for elements in periods 3 and 4 of the periodic table. Lanthanide and actinide aqua ions have a solvation number of 8 or 9. The strength of the bonds between the metal ion and water molecules in the primary solvation shell increases with the electrical charge, z, on the metal ion and decreases as its ionic radius, r, increases. Aqua ions are subject to hydrolysis. The logarithm of the first hydrolysis constant is proportional to z2/r for most aqua ions.
Degrees of carbonate hardness (dKH or °KH; the K is from the German Karbonathärte) is a unit of water hardness, specifically for temporary or carbonate hardness. Carbonate hardness is a measure of the concentration of carbonates such as calcium carbonate (CaCO3) and magnesium carbonate (MgCO3) per volume of water. Specifically, 1 dKH is defined as 17.86 milligrams (mg) of calcium carbonate per litre of water, i.e. 17.86 ppm. Since a mole of calcium carbonate weighs 100.09 grams, 1 dKH is equivalent to 0.17832 mmol per litre.
The residual sodium carbonate (RSC) index of irrigation water or soil water is used to indicate the alkalinity hazard for soil. The RSC index is used to find the suitability of the water for irrigation in clay soils which have a high cation exchange capacity. When dissolved sodium in comparison with dissolved calcium and magnesium is high in water, clay soil swells or undergoes dispersion which drastically reduces its infiltration capacity.
A Maucha diagram, or Maucha symbol, is a graphical representation of the major cations and anions in a chemical sample. R. Maucha published the symbol in 1932.