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From Wikipedia, the free encyclopedia
This article is about the mineral. For the aircraft manufacturer, see Belite Aircraft.
Belite is an industrial mineral important in Portland cement manufacture. Its main
constituent is dicalcium silicate, Ca2SiO4, sometimes formulated as 2 CaO · SiO2 (C2S
in cement chemist notation).
Etymology[edit]
The name was given by Törnebohm in 1897 to a crystal identified in microscopic
investigation of Portland cement.[1] Belite is a name in common use in the cement
industry, but is not a recognised mineral name. It occurs naturally as the mineral larnite,
the name being derived from Larne, Northern Ireland, the closest town to Scawt
Hill where it was discovered.[2]
Composition and structure[edit]
Simplified crystal structure of belite
The belite found in Portland cement differs in composition from pure dicalcium silicate. It
is a solid solution and contains minor amounts of other oxides besides CaO and SiO2. A
typical composition:[3]
Oxide Mass %
CaO 63.5
SiO2 31.5
Al2O3 2.1
Fe2O3 0.9
MgO 0.5
SO3 0.1
Na2O 0.1
K2O 0.9
TiO2 0.2
P2O5 0.2
4) ions, provided that for each sulfate ion, two aluminate (AlO
5−
Polymorphs[edit]
Dicalcium silicate is stable, and is readily prepared from reactive CaO and SiO2 at
300 °C. The low temperature form is γ-belite, or lime olivine. This form does not hydrate,
and is avoided in cement manufacture.
As the temperature rises, it passes through several polymorphic states:
>1425 α Hexagonal
500-680 β Monoclinic
<500 γ Orthorhombic
Hydration[edit]
Belite is the mineral in Portland cement responsible for development of "late" strength.
The other silicate, alite contributes "early" strength, due to its higher reactivity. Belite
reacts with water (roughly) to form calcium silicate hydrates (C-S-H)
and portlandite (Ca(OH)2) according to the reaction:
This rapid reaction is "chemically analogue" to the slow natural hydration
of forsterite (the magnesium end-member of olivine) leading to the formation
of serpentine and brucite in nature, although the kinetic of hydration of poorly
crystallized artificial belite is much faster than the slow weathering of well crystallized
Mg-olivine under natural conditions.
The hydrate phase, [3 CaO · 2 SiO2 · 3 H2O], is referred to as the "C-S-H" phase. It
grows as a mass of interlocking needles that provide the strength of the hydrated
cement system. Relatively high belite reactivity is desirable in Portland cement
manufacture, and the formation of the unreactive γ-form must be rigorously avoided.
This is achieved by rapid cooling, forming crystals that are small, distorted and highly
defective. Defects provide sites for initial water attack. Failure to cool the clinker rapidly
leads to inversion of belite to the γ-form. The γ-form has a substantially different
structure and density, so that inversion leads to degradation of the crystal and its
surrounding matrix, and can also trigger decomposition of the neighboring alite. This is
observed macroscopically as "dusting": the clinker nodules fall to a fine dust.
Detection[edit]