Halite: Difference between revisions
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[[Category:Halite]] [[Category: | [[Category:Halite]] [[Category:Hschwarz]] [[Category:R-MSteiger]] [[Category:inProgress]] [[Category:Chloride]] [[Category:Salt]] |
Revision as of 13:36, 12 January 2012
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Authors: Hans-Jürgen Schwarz, Nils Mainusch
English version by Christa Gerdwilker
back to Chloride
Halite[1][2][3] | |
Mineralogical name | Halite |
Chemical name | Sodium chloride |
Trivial name | Common Salt, Rock Salt |
Chemical formula | NaCl |
Other forms | Natriumchlorid Dihydrat/Hydrohalit (NaCl•2H2O)[4] |
Crystal system | cubic |
Crystal structure | |
Deliquescence humidity 20°C | 75.7% (10°C), 75.3% (25°C) |
Solubility (g/l) at 20°C | 358 g/l |
Density (g/cm³) | 2.163 g/cm3 |
Molar volume | 27.02 cm3/mol |
Molar weight | 58.44 g/mol |
Transparency | transparent to translucent |
Cleavage | perfect |
Crystal habit | cubic crystal, granular, massive aggregates |
Twinning | none |
Phase transition | |
Chemical behavior | |
Comments | slightly watersoluble |
Crystal Optics | |
Refractive Indices | n=1.544 |
Birefringence | |
Optical Orientation | isotropic |
Pleochroism | |
Dispersion | |
Used Literature | |
{{{Literature}}} |
Abstract[edit]
Halite origins[edit]
Sodium chloride is obtained through mining or derived from the sea or salt lakes and is commonly used for cooking or as road gritting salt.
The salt content of sea water is approx. 2,7 M.%.
Causes of halite formation on monuments[edit]
Contact with materials containing soluble sodium-based ingredients can result in the efflorescence of sodium chloride on monuments. A primary example is the high sodium content of cements. Contamination with sodium and chloride ions can also occur through contact with salt laden ground or surface water. A range of cleaning materials (e.g. acidic and caustic cleaners) and especially previously used restoration materials (e.g. water glass) can introduce sodium and chloride ions into monuments. Further common sources of halite are rock salt used in road gritting which predominantly consists of sodium chloride, as well as salt laden seawater in coastal areas.
Solubility behavior[edit]
The commonly occurring halite found in northern Germany has a solubility of 358 g/l (20°C) and thus belongs to the group of very soluble and, therefore, easily mobilized salts. Its solubility changes comparatively little within a temperature range of 10 -30°C.
Temperature | 10°C | 20°C | 40°C |
Solubility [g/l] | 356,5 | 358,8 | 364,2 |
Hygroscopicity[edit]
Halite’s deliquescence humidity of approx. 75% is often crossed in the climate of northern Europe. Temperature variations hardly affect the deliquescence point of halite which is illustrated below in comparison with potassium nitrate and natrite.
Moisture sorption:
Theoretically 1g NaCl can absorb 4,3g moisture. The moisture sorption during varying relative humidity levels is:
Relative humidity during storge/salt phase | NaCl |
87% RH | 153 |
81% RH | 22 |
79% RH | 7 |
Crystallization pressure[edit]
The crystallization of halite from a water-based solution results in a crystallization pressure of 55,4-65,4 N/mm2 [Winkler:1975]Title: Stone: Properties, Durability in Man´s Environment
Author: Winkler, Erhard M.
(for comparison, the crystallization pressure of different salts can range from 7,2-65,4 N/mm2). These values need to be considered in conjunction with temperature and concentration and can, therefore, only act as indicators of damage potential in relation to salt crystallization pressure. In comparison to other salts, the crystallization pressure of halite is extremely high.
Hydration behavior[edit]
Under normal conditions only the unhydrated form of halite exists. Only at a temperature of below 0.15 °C does a saturated water-based sodium chloride solution result in the precipitation of a deposit of dihydrate hydrohalite[4].
Microscopy[edit]
Laboratory examinations[edit]
Sodium chloride crystals can be reliably identified on the basis of morphological features. Individual particles usually form cubic or octahedral shapes and, therefore, clearly display right angles in their crystal construction.
Refractive index: nD = 1,544
Crystal category: cubic
Examinations under the polarising microscope:
Together with potassium chloride, sodium chloride is one of the few salts belonging to the cubic crystal system which cause damage to masonry. Because of its isotropic internal structure it does not display birefringence.
The classification of the refractive index occurs by immersion method in a standard oil with a refractive index of nD =1,518. Halite crystals display the same optical density in every direction so that the speed and orientation of linear polarised light waves are not distorted. When viewed between crossed polars, the crystals are not visible but appear (independent of orientation) extinguished.
Differentiating of halite from similar salts:
The group of isotropic salts causing masonry damage consists of halite, sylvine and fluorite. All these phases can be differenciated easily.
Salt phase | Identification features |
Sylvine KCl | Refractive index under 1,518. |
Fluorite CaF2 | Refractive index under 1,518, barely water soluble. |
Images of salts and salt damage[edit]
In situ[edit]
Under the polarising microscope[edit]
Weblinks[edit]
- ↑ http://webmineral.com/data/Halite.shtml accessed 28.07.2010
- ↑ http://www.mindat.org/min-1804.html accessed 28.07.2010
- ↑ http://www.mineralienatlas.de/lexikon/index.php/MineralData?mineral=Halit accessed 28.07.2010
- ↑ 4.0 4.1 http://www.mineralienatlas.de/lexikon/index.php/MineralData?mineral=Hydrohalit gelesen 28.07.2010 Cite error: Invalid
<ref>
tag; name "hydrohalit" defined multiple times with different content
Literature[edit]
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