出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2016/10/30 18:47:16」(JST)
Names | |
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IUPAC name
Sodium metasilicate
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Other names
Liquid glass
Waterglass |
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Identifiers | |
CAS Number
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6834-92-0 Y |
Abbreviations | E550 |
ChEBI | CHEBI:60720 Y |
ChemSpider | 21758 Y |
ECHA InfoCard | 100.027.193 |
EC Number | 229-912-9 |
Jmol 3D model | Interactive image |
MeSH | Sodium+metasilicate |
PubChem | 23266 |
RTECS number | VV9275000 |
UN number | 3253 |
InChI
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SMILES
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Properties | |
Chemical formula
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Na2SiO3 |
Appearance | White to greenish opaque crystals |
Density | 2.61 g cm−3 |
Melting point | 1,088 °C (1,990 °F; 1,361 K) |
Solubility in water
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22.2 g/100 ml (25°C) 160.6 g/100 ml (80°C) |
Solubility | insoluble in alcohol |
Refractive index (nD)
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1.52 |
Thermochemistry | |
Specific
heat capacity (C) |
111.8 J/mol K |
Std molar
entropy (S |
113.71 J K−1 mol−1 |
Std enthalpy of
formation (ΔfH |
−1561.43 kJ mol−1 |
Gibbs free energy (ΔfG˚)
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-1427 kJ/mol |
Hazards | |
Safety data sheet | Avantor Performance Materials |
EU classification (DSD)
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C |
R-phrases | R34, R37 |
S-phrases | (S1/2), S13, S24/25, S36/37/39, S45 |
NFPA 704 |
0
2
0
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Lethal dose or concentration (LD, LC): | |
LD50 (median dose)
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1153 (rat, oral) |
Related compounds | |
Other anions
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Sodium carbonate |
Other cations
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Potassium silicate |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Y verify (what is YN ?) | |
Infobox references | |
Sodium silicate is the common name for compounds with the formula Na2(SiO2)nO. A well-known member of this series is sodium metasilicate, Na2SiO3. Also known as waterglass or liquid glass, these materials are available in aqueous solution and in solid form. The pure compositions are colourless or white, but commercial samples are often greenish or blue owing to the presence of iron-containing impurities.
They are used in cements, passive fire protection, textile and lumber processing, refractories, and automobiles. Sodium carbonate and silicon dioxide react when molten to form sodium silicate and carbon dioxide:[1]
Anhydrous sodium silicate contains a chain polymeric anion composed of corner-shared {SiO4} tetrahedral, and not a discrete SiO32− ion.[1] In addition to the anhydrous form, there are hydrates with the formula Na2SiO3·nH2O (where n = 5, 6, 8, 9) which contain the discrete, approximately tetrahedral anion SiO2(OH)22− with water of hydration. For example, the commercially available sodium silicate pentahydrate Na2SiO3·5H2O is formulated as Na2SiO2(OH)2·4H2O and the nonahydrate Na2SiO3·9H2O is formulated as Na2SiO2(OH)2·8H2O.[2]
In industry, the various grades of sodium silicate are characterized by their SiO2:Na2O weight ratio (weight ratios can be converted to molar ratios by multiplication with 1.032), which can vary between 2:1 and 3.75:1.[3] Grades with this ratio below 2.85:1 are termed alkaline. Those with a higher SiO2:Na2O ratio are described as neutral.
Water glass[4] was defined in Von Wagner's Manual of Chemical Technology (1892 translation) as any of the soluble alkaline silicates, first observed by Jean Baptist van Helmont circa 1640 as a fluid substance made by melting sand with excess alkali.[5][6] Glauber made what he termed "liquor silicum" in 1646 from potash and silica.[7] Johann Nepomuk von Fuchs, in 1818, obtained what is now known as water glass by treating silicic acid with an alkali, the result being soluble in water, "but not affected by atmospheric changes".[8][9] Von Wagner distinguished soda, potash, double (soda and potash), and fixing (i.e., stabilizing) as types of water glass. The fixing type was "a mixture of silica well saturated with potash water glass and a sodium silicate" used to stabilize inorganic water color pigments on cement work for outdoor signs and murals.
Sodium silicate is a white powder that is readily soluble in water, producing an alkaline solution. It is one of a number of related compounds which include sodium orthosilicate, Na4SiO4, sodium pyrosilicate, Na6Si2O7, and others. All are glassy, colourless, and soluble in water.
Sodium silicate is stable in neutral and alkaline solutions. In acidic solutions, the silicate ion reacts with hydrogen ions to form silicic acid, which when heated and roasted forms silica gel, a hard, glassy substance.
Sodium silicate is commonly manufactured using a reaction in liquid phase or in solid phase. Both processes use alkaline and quartz sand as raw materials.
A mixture of caustic soda, quartz sand, and water is prepared in a mixing tank, then fed into a reactor, where steam is introduced. The reaction is
n SiO2 + 2 NaOH → Na2O•nSiO2 + H2O
Sodium carbonate and sodium sulfate melt at temperatures far below that of silica. (<900°C vs >1600°C) Either is melted, and silica dissolved into the molten material, where it reacts to form sodium silicate.
In 1990, 4M tons of alkali metal silicates were produced. The main applications were in detergents, paper, water treatment, and construction materials.[3]
The largest application of sodium silicate solutions is a cement for producing cardboard.[3] When used as a paper cement, the tendency is for the sodium silicate joint eventually to crack within a few years, at which point it no longer holds the paper surfaces cemented together.
Sodium silicate is frequently used in drilling fluids to stabilize borehole wells and to avoid the collapse of bore walls. It is particularly useful when drill holes pass through argillaceous formations containing swelling clay minerals such as smectite or montmorillonite.
Concrete treated with a sodium silicate solution helps to significantly reduce porosity in most masonry products such as concrete, stucco, and plasters. A chemical reaction occurs with the excess Ca(OH)2 (portlandite) present in the concrete that permanently binds the silicates with the surface, making them far more durable and water repellent. This treatment generally is applied only after the initial cure has taken place (7 days or so depending on conditions). These coatings are known as silicate mineral paint.
It is used in detergent auxiliaries such as complex sodium disilicate and modified sodium disilicate. The detergent granules gain their ruggedness from a coating of silicates.[3]
Water glass is used as coagulant/deflocculant agent in wastewater treatment plants. Waterglass binds to colloidal molecules, creating larger aggregates that sink to the bottom of the water column. The microscopic negatively charged particles suspended in water interact with sodium silicate. Their electrical double layer collapses due to the increase of ionic strength caused by the addition of sodium silicate (doubly negatively charged anion accompanied by two sodium cations) and they subsequently aggregate. This process is called coagulation/deflocculation.[3]
Water glass is a useful binder of solids, such as vermiculite and perlite. When blended with the aforementioned lightweight aggregates, water glass can be used to make hard, high-temperature insulation boards used for refractories, passive fire protection and high temperature insulations, such as moulded pipe insulation applications. When mixed with finely divided mineral powders, such as vermiculite dust (which is common scrap from the exfoliation process), one can produce high temperature adhesives. The intumescence disappears in the presence of finely divided mineral dust, whereby the waterglass becomes a mere matrix. Waterglass is inexpensive and abundantly available, which makes its use popular in many refractory applications.
Sodium silicate solution is used as a fixative for hand dyeing with reactive dyes that require a high pH to react with the textile fiber. After the dye is applied to a cellulose-based fabric, such as cotton or rayon, or onto silk, it is allowed to dry, after which the sodium silicate is painted on to the dyed fabric, covered with plastic to retain moisture, and left to react for an hour at room temperature.[10]
Sodium silicates are inherently intumescent. They come in prill (solid beads) form, as well as the liquid, water glass. The solid sheet form (Palusol) must be waterproofed to ensure long-term passive fire protection (PFP).
Standard, solid, bead-form sodium silicates have been used as aggregate within silicone rubber to manufacture plastic pipe firestop devices. The silicone rubber was insufficient waterproofing to preserve the intumescing function and the products had to be recalled, which is problematic for firestops concealed behind drywall in buildings.
Pastes for caulking purposes are similarly unstable. This, too, has resulted in recalls and even litigation. Only 3M's "Expantrol" version, which has an external heat treatment that helps to seal the outer surface, as part of its process standard, has achieved sufficient longevity to qualify for DIBt approvals in the US for use in firestopping.
Not unlike other intumescents, sodium silicate, both in bead form and in liquid form, are inherently endothermic, due to liquid water in the water glass and hydrates in the prill form. The absence in the US of mandatory aging tests, whereby PFP systems are made to undergo system performance tests after the aging and humidity exposures, are at the root of the continued availability, in North America, of PFP products that can become inoperable within weeks of installation. Indiscriminate use of sodium silicates without proper waterproofing measures are contributors to the problems and risk. When sodium silicates are adequately protected, they function extremely well and reliably for long periods. Evidence of this can be seen in the many DIBt approvals for plastic pipe firestop devices using Palusol, which use waterproofed sodium silicate sheets.
Sodium silicate was also used as an egg preservation agent through the early 20th century with large success. When fresh eggs are immersed in it, bacteria which cause the eggs to spoil are kept out and water is kept in. Eggs can be kept fresh using this method for up to five months. When boiling eggs preserved this way, it is well advised to pin-prick the egg to allow steam to escape because the shell is no longer porous.[11]
Sodium silicate is used, along with magnesium silicate, in muffler repair and fitting paste. When dissolved in water, both sodium silicate and magnesium silicate form a thick paste that is easy to apply. When the exhaust system of an internal combustion engine heats up to its operating temperature, the heat drives out all of the excess water from the paste. The silicate compounds that are left over have glass-like properties, making a temporary, brittle repair.
Sodium silicate is also used currently as an exhaust system joint and crack sealer for repairing mufflers, resonators, tailpipes, and other exhaust components, with and without fiberglass reinforcing tapes. In this application, the sodium silicate (60–70%) is typically mixed with kaolin (40-30%), an aluminium silicate mineral, to make the sodium silicate "glued" joint opaque. The sodium silicate, however, is the high-temperature adhesive; the kaolin serves simply as a compatible high-temperature coloring agent. Some of these repair compounds also contain glass fibres to enhance their gap-filling abilities and reduce brittleness.
Sodium silicate can be used to fill gaps within the head gasket. Commonly used on aluminum alloy cylinder heads, which are sensitive to thermally induced surface deflection. This can be caused by many things including head-bolt stretching, deficient coolant delivery, high cylinder head pressure, overheating, etc.
"Liquid glass" (sodium silicate) is added to the system through the radiator, and allowed to circulate. Sodium silicate is suspended in the coolant until it reaches the cylinder head. At 100–105°C, sodium silicate loses water molecules to form a glass seal with a remelt temperature above 810°C.
A sodium silicate repair can last two years or longer. The repair occurs rapidly, and symptoms disappear instantly. This repair only works when the sodium silicate reaches its "conversion" temperature at 100–105°C. Contamination of engine oil is a serious possibility in situations in which a coolant-to-oil leak is present. Sodium silicate (glass particulate) contamination of lubricants is detrimental to their function.
Sodium silicate solution is used to inexpensively, quickly, and permanently disable automobile engines. Running an engine with about 2 liters of a sodium silicate solution instead of motor oil causes the solution to precipitate, catastrophically damaging the engine's bearings and pistons within a few minutes.[12] In the United States, this procedure was used to comply with requirements of the Car Allowance Rebate System (CARS) program.[12][13]
Sodium silicate flocculant properties are also used to clarify wine and beer by precipitating colloidal particles. As a clearing agent, though, sodium silicate (water glass) is sometimes confused with isinglass which is prepared from collagen extracted from the dried swim bladders of sturgeon and other fishes. Eggs preserved in a bucket of waterglass gel, and their shells, are sometimes also used (baked and crushed) to clear wine.[14]
Sodium silicate gel is also used as a substrate for algal growth in aquaculture hatcheries.
A mixture of sodium silicate and sawdust has been used in between the double skin of certain safes. This not only makes them more fire resistant, but also makes cutting them open with an oxyacetylene torch extremely difficult due to the smoke emitted.
When crystals of a number of metallic salts are dropped into a solution of water glass, simple or branching stalagmites of coloured metal silicates are formed. This phenomenon has been used by manufacturers of toys and chemistry sets to provide instructive enjoyment to many generations of children from the early 20th century until the present. An early mention of crystals of metallic salts forming a "chemical garden" in sodium silicate is found in the 1946 Modern Mechanix magazine.[15] Metal salts used included the sulfates and/or chlorides of copper, cobalt, iron, nickel, and manganese.
Sodium silicate is used as a deflocculant in casting slips helping reduce viscosity and the need for large amounts of water to liquidize the clay body. It is also used to create a crackle effect in pottery, usually wheel-thrown. A vase or bottle is thrown on the wheel, fairly narrow and with thick walls. Sodium silicate is brushed on a section of the piece. After 5 minutes, the wall of the piece is stretched outward with a rib or hand. The result is a wrinkled or cracked look.
It is also the main agent in "magic water", which is used when joining clay pieces, especially if the moisture level of the two differs.[16]
Sodium silicate with additives was injected into the ground to harden it and thereby to prevent further leakage of highly radioactive water from the Fukushima Daiichi nuclear power plant in Japan in April, 2011.[17] The residual heat carried by the water used for cooling the damaged reactors accelerated the setting of the injected mixture.
On June 3, 1958, the USS Nautilus, the world's first nuclear submarine, visited Everett and Seattle. In Seattle, crewmen dressed in civilian clothing were sent in to secretly buy 140 quarts of an automotive product containing sodium silicate (originally identified as Stop Leak) to repair a leaking condenser system. The Nautilus was en route to the North Pole on a top secret mission to cross the North Pole submerged.[18]
A historical use of the adhesive properties of sodium silicates is the production of paper cartridges for black powder revolvers produced by Colt's Manufacturing Company during the period from 1851 until 1873, especially during the American Civil War. Sodium silicate was used to seal combustible nitrated paper together to form a conical paper cartridge to hold the black powder, as well as to cement the lead ball or conical bullet into the open end of the paper cartridge. Such sodium silicate cemented paper cartridges were inserted into the cylinders of revolvers, thereby speeding the reloading of cap-and-ball black powder revolvers. This use largely ended with the introduction of Colt revolvers employing brass-cased cartridges starting in 1873.[19][20] Similarly, sodium silicate was also used to cement the top wad into brass shotgun shells, thereby eliminating any need for a crimp at the top of the brass shotgun shell to hold a shotgun shell together. Reloading brass shotgun shells was widely practiced by self-reliant American farmers during the 1870s, using the same waterglass material that was also used to preserve eggs. The cementing of the top wad on a shotgun shell consisted of applying from three to five drops of waterglass on the top wad to secure it to the brass hull. Brass hulls for shotgun shells were superseded by paper hulls starting around 1877. The newer paper-hulled shotgun shells used a roll crimp in place of a waterglass-cemented joint to hold the top wad in the shell. However, whereas brass shotshells with top wads cemented with waterglass could be reloaded nearly indefinitely (given powder, wad, and shot, of course), the paper hulls that replaced the brass hulls could be reloaded only a few times.
However, subsequently an article pointed out that the substance prepared by Basil Valentine in 1520, by Agricola in 1550, by van Helmont around 1640, and by Glauber in 1648 was not the waterglass that Fuchs produced in 1818. See:
Wikimedia Commons has media related to Sodium silicates. |
Sodium compounds
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Chemical formulas
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関連記事 | 「glass」「water」「watering」 |
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