Rawmill

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In cement manufacturing, a raw mill is a type of industrial equipment used to crush, grind, and proportion raw materials into a uniform mixture known as raw meal (or rawmix), which is subsequently processed in a cement kiln to produce clinker, which is then ground to make cement in the cement mill.[1]

The raw milling stage of the process effectively defines the chemistry (and therefore physical properties) of the finished cement, and has a large effect upon the efficiency of the whole manufacturing process.

A medium-sized dry process roller mill

The history of the development of the technology of raw material grinding defines the early history of cement technology. Other stages of cement manufacture used existing technology in the early days. Early hydraulic materials such as hydraulic limes, natural cements and Parker's Roman cement were all based on "natural" raw materials, burned "as-dug". Because these natural blends of minerals occur only rarely, manufacturers were interested in making a fine-grained artificial mixture of readily available minerals such as limestone and clay that could be used in the same way. A typical problem would be to make an intimate mixture of 75% chalk and 25% clay, and burn this to produce an ”artificial cement". The development of the "wet" method of producing fine-grained clay in the ceramics industry afforded a means of doing this. For this reason, the early cement industry used the "wet process", in which the raw materials are ground together with water, to produce a slurry, containing 20–50% water. Both Louis Vicat and James Frost used this technique in the early 19th century, and it remained the only way of making rawmix for Portland cement until 1890. A modification of the technique used by the early industry was "double-burning", in which a hard limestone would be burned and slaked before combining with clay slurry. This technique avoided the grinding of hard stone, and was employed by, among others, Joseph Aspdin. Early grinding technology was poor, and early slurries were made thin, with a high water content. The slurry was then allowed to stand in large reservoirs ("slurry-backs") for several weeks. Large, un-ground particles would drop to the bottom, and excess water rose to the top. The water was periodically decanted until a stiff cake, of the consistency of pottery clay, was left. This was sliced up, discarding the coarse material at the bottom, and burned in the kiln. Wet grinding is comparatively energy-efficient, and so when good dry-grinding equipment became available, the wet process continued in use throughout the 20th century, often employing equipment that Josiah Wedgwood would have recognized.

Materials ground

Rawmixes are formulated to contain a correctly balanced chemistry for the production of calcium silicates (alite and belite) and fluxes (aluminate and ferrite) in the kiln. Chemical analysis data in cement manufacture are expressed in terms of oxides, and the most important of these in rawmix design are SiO2, Al2O3, Fe2O3 and CaO. In principle, any material that can contribute any of these oxides can be used as a rawmix component. Because the major oxide required is CaO, the most prevalent rawmix component is limestone, while the others are mostly contributed by clay or shale. Minor adjustments to the chemistry are made by smaller additions of materials such as those shown below.

Typical rawmix component chemical analyses:

Oxide Gray Limestone White Limestone Marl Clay Sand Millscale Kaolin Bauxite Fly ash
SiO26.62.114.161.698.01.346.111.148.1
Al2O31.50.33.317.50.91.238.554.426.5
Fe2O30.70.131.37.50.1396.80.359.76
CaO48.453.743.81.10.10.30.30.64.7
MgO2.00.80.71.10.00.60.10.11.2
Na2O0.070.020.070.50.020.110.010.050.3
K2O0.270.080.431.90.370.050.090.051.3
TiO20.060.020.150.80.060.300.92.11.5
Mn2O30.030.010.020.1200.6300.090.07
LoI95040.042.735.86.80.3013.720.89.1

Note: LoI950 is the Loss on ignition at 950 °C, and represents (approximately) the components lost during kiln processing. It consists mainly of CO2 from carbonates, H2O from clay hydrates, and organic carbon.

Using these materials, typical rawmixes could be composed:

  • Mix 1: General-purpose cement: 88.0% gray limestone, 8.9% clay, 2.2% sand and 0.9% millscale.
  • Mix 2: Sulfate-resisting cement: 87.6% gray limestone, 5.2% clay, 5.0% sand and 2.2% millscale.
  • Mix 3: White cement: 82.3% white limestone, 6.8% kaolin and 10.9% sand.

The chemical analyses of these rawmixes would be:

Oxide Mix 1 Mix 2 Mix 3
SiO213.4613.9115.55
Al2O32.912.302.96
Fe2O32.163.140.14
CaO42.6942.4744.23
MgO1.861.820.67
Na2O0.110.090.02
K2O0.410.350.11
TiO20.130.100.09
Mn2O30.040.050.01
LoI95035.835.436.1

The raw materials and mixes shown are only "typical": considerable variations are possible depending on the raw materials available.

Control of minor elements

Apart from the major oxides (CaO, SiO2, Al2O3 and Fe2O3) the minor oxides are, at best, diluents of the clinker, and may be deleterious. However, cement raw materials are for the most part dug from the Earth's crust and contain most of the elements in the periodic table in some amount. The manufacturer therefore selects materials so that the deleterious effects of minor elements are minimized or kept under control. Minor elements that are frequently encountered are as follows:

  • Fluorine is beneficial to the kiln process in that it allows alite to form at lower temperature. However, at levels above 0.25% in the clinker, delayed and erratic cement setting time results.
  • Alkali metals (primarily sodium and potassium) cause processing problems because they form volatile salts in the kiln system. These evaporate in the kiln burning zone and re-condense in the cooler regions of the preheater, causing blockages. Alkalis are also deleterious to concrete, potentially causing alkali silica reaction. For this reason, many standards limit alkalis (typically expressed as "total equivalent soda" which is Na2O + 0.658 K2O). Typical specification limits are in the range 0.5–0.8%.
  • MgO causes problems at levels over 2.5%. Small amounts are accommodated in solid solution in the clinker minerals, but above 2.5%, "free" MgO exists in the clinker as periclase. This can slowly hydrate to Mg(OH)2 with expansion in the hardened concrete, causing cracking. Careful processing of the clinker to keep the periclase in a microcrystalline form allows levels up to 5% to be managed without serious effect. All standards limit MgO, typical limits being in the range 4-6%.
  • P2O5 at levels above 0.5% starts to cause slow setting and low clinker reactivity.
  • Chlorine produces very volatile salts and consequent preheater blockages, and is usually limited to below 0.1% in rawmix.
  • TiO2 is ubiquitous, but is rarely present at levels (~1%) that might cause problems.
  • Chromium can end up as chromates (Cr[VI]) in cement, particularly when the clinker is high in sulfate. Chromates cause allergic contact dermatitis in cement users, and for this reason cement Cr[VI] content is limited in many standards to 0.0002%. Typical natural rawmixes contain around 0.01% Cr2O3, and at this level, Cr[VI] formation can be controlled. Chromium present in the cement as Cr[III] is of no consequence.
  • Mn2O3 is not deleterious, acting as a substitute for iron. But it contributes more color to the cement than iron, and high-Mn2O3 cements (>1%) are almost black.
  • ZnO is encountered in some rawmix additives (as well as tires used as kiln fuel). At levels above 0.2%, it causes slow setting and low clinker reactivity.
  • Strontium and barium act as calcium replacements, and only start to reduce clinker reactivity at levels of 1.5% and 0.2% respectively.
  • Toxic heavy metals: among these, low levels of arsenic, selenium, cadmium, antimony and tungsten are not a problem, because they are absorbed in the basic clinker structure as anions. On the other hand, mercury, thallium and lead must be carefully controlled because they can be emitted as volatile halides in the kiln exhaust.

Wet rawmills

Dry rawmills

References

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