Halite
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 | Sodium chloride dihydrate/Hydrohalite (NaCl•2H2O)[4] |
Crystal system | cubic |
Crystal structure | |
Deliquescence humidity 20°C | 75.4% [Steiger etal: 2104]The entry doesn't exist yet. |
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 | water soluble |
Crystal Optics | |
Refractive Indices | n=1.544 |
Birefringence | |
Optical Orientation | isotropic |
Pleochroism | |
Dispersion | |
Used Literature | |
Abstract[edit]
Occurrence[edit]
Sodium chloride is obtained through mining or derived from the sea or salt lakes and is commonly used for cooking or as deicing salt for roads.
The sodium chloride content of sea water is around 2.7 M.%.
Origin of the halite found on monuments[edit]
Sodium chloride can enter buildings or monuments when these are in contact with materials containing this salt or even other salts containing either sodium or chloride, that might combine to produce NaCl in or efflorescence on them. 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 alkaline cleaners or combination of them), or previously used restoration materials (e.g., water glass) as well as Portland cement, can introduce sodium and chloride ions into monuments. Further common and important sources are deicing salts and maritime environments where the air and fogs may contain a significant amount of sodium chloride in suspension or dissolved in droplets.
Solubility behavior[edit]
The commonly occurring halite has a solubility of 358 g/l (20°C) and can be considered a very soluble and, therefore, easily mobilized salt. 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 has a deliquescence humidity of about 75% RH, therefore it tends to pick up moisture easily in most temperate climates.
0°C | 10°C | 20°C | 30°C | 40°C | 50°C |
75.9%r.h. | 75.6%r.h. | 75.4%r.h. | 75.2%r.h. | 75.2%r.h. | 74.8%r.h. |
Moisture sorption:
Theoretically 1g NaCl can take up 4.3g of moisture, i.e., water vapor. 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 |
Hydration behavior[edit]
Under normal environmental conditions only halite will crystallize out of a saturated solution. The hydrated form, dihydrate hydrohalite[4] will only precipitate out at temperatures below 0.15°C.
Microscopy[edit]
Laboratory analysis[edit]
Sodium chloride crystals can be reliably identified on the basis of their 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
Examination by polarized microscopy:
There are few salts belonging to the cubic crystal system which can be found in masonry, i.e., sodium chloride (halite), potassium chloride (sylvite) and calcium fluoride (flourite). Only the two first salts are highly soluble and therefore they are the ones that can cause damage to the masonry. Because of its isotropic internal structure these salts do not display birefringence.
The refractive index can be measured with the immersion method by using 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 polarized light waves are not distorted, therefore, when viewed between crossed polars, the crystals are not visible, i.e., they show "extinction".
Differentiation of halite from similar salts:
The three above mentioned isotropic salts can be easily differentiated.
Salt phase | Identification features |
Sylvine KCl | Refractive index below 1,518. |
Fluorite CaF2 | Refractive index below 1,518, barely water soluble. |
Images of salts and salt damage[edit]
In situ[edit]
Under the polarizing microscope[edit]
Scanning Electron Microscope photomicrographs[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 accessed 28.07.2010
Literature[edit]
[Dana:1951] | Dana E.S. (eds.) Dana J.D. (1951): Dana's System of Mineralogy, 7, Wiley & Sons | |
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[Steiger] | The entry doesn't exist yet. | |
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[Steiger.etal:2014] | Steiger, Michael; Charola A. Elena; Sterflinger, Katja (2014): Weathering and Deterioration. In: Siegesmund S.; Snethlage R. (eds.): Stone in Architecture, Springer Verlag Berlin Heidelberg, 223-316, 10.1007/978-3-642-45155-3_4. | |
[Vogt.etal:1993] | Vogt, R.; Goretzki, Lothar (1993): Der Einfluss hygroskopischer Salze auf die Gleichgewichtsfeuchte und Trocknung anorganischer Baustoffe, unveröffentlichter Bericht. | |
[Winkler:1975] | Winkler, Erhard M. (1975): Stone: Properties, Durability in Man´s Environment, Springer Verlag, Wien |
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