Chemistry of inorganic compounds – Treating mixture to obtain metal containing compound – Group iiia metal or beryllium
Reexamination Certificate
2001-11-29
2004-11-09
Bos, Steven (Department: 1754)
Chemistry of inorganic compounds
Treating mixture to obtain metal containing compound
Group iiia metal or beryllium
C423S116000, C423S117000, C423S158000, C423S163000, C423S166000, C423S127000, C423S129000, C423S164000, C423S165000, C423S600000
Reexamination Certificate
active
06814947
ABSTRACT:
The invention relates to the production and use of calcium compounds containing water of crystallisation, in particular of ionogenic bound compounds on calcium aluminatehydrate and calcium aluminatehydrate salt basis, preferably of the corresponding sulfates, silicates, carbonates, fluorides and/or chlorides. The thus obtained different compounds are useful as fillers or extra white pigments in the production and surface-coating of paper, paperboard or card, in the production of paints and lacquers, such as in the production of paints and lacquers for indoor and outdoor uses or for the rust-protection of metals, as a flame-retardant filler for fire-protecting construction materials, insulating materials, mortars, wallpapers, cardboards, papers and paints as well as fillers for producing plasterboards and construction slabs, respectively, mortars, paints or as an hydraulically active additive for producing swelling cements, swelling plasters and screeds as well as a swelling component for explosion-protected explosives.
Fillers and additives, in particular mineral fillers and additives are used in great extent i.a. in the plastic, paint, tire and ceramic industries as well as in the construction material industries, in particular in pulp and paper industries.
Papier, paperboard and card are produced for example from an aqueous suspension essentially by dehydrating, drying and pressing it. Besides fiber materials like cellulose and wood chips, i.a. also fillers, preferably the natural minerals kaolin (aluminosilicates) and chalk (calcium carbonate) are used. Depending on the requirements in regard to the quality of paper and paperboard, respectively, (printability, whiteness, gloss, strength etc.) the amount of added fillers, however, is limited. Typically it is from 10 to 25% by weight, based on the weight of the paper. In Germany in the paper industries about 3 millions of tons of fillers per year are consumed.
Mineral natural fillers have to be degraded, purified (for example washed) and milled. Higher quality demands of the filler processors have resulted in that more synthetic precipitates, preferably precipitated calcium carbonate, are used. Furthermore, several approaches have been made to use plaster (calcium sulfate) as a filler, in particular the reaction products obtained in vast amounts from fuming gas desulfurisation installations of power plants (REA plaster). However, until yet these were not successful since calcium sulfate is water-soluble up to a concentration of about 2 g SO
4
2−
/l and no sufficient whiteness has been achieved. In the paper production an accumulation of dissolved calcium sulfate in the process water cycle occurs and therefore undesired deposits and microbiologic problems (for instance by bacteria like desulfovibrio or desulfazomaculum) arose.
In the paper industries a calcium aluminum sulfate precipitate is used as spreading pigment for high quality papers. This product is obtained from the starting materials aluminum sulfate and chalkhydrate according to the following reaction equation:
Al
2
(SO
4
)
3
+7Ca(OH)
2
+25H
2
O→Ca
6
Al
2
((OH)
4
)SO
4
)
3
*25H
2
O+Ca(OH)
2
Since the above chemical reaction only proceeds spontaneously at a high pH of>12, an excess of chalkhydrate is necessary. Furthermore, in this method only suspensions having a solid content of <50% can be obtained, which are known i.a. as satin-white.
A further great application demand for mineral fillers exists in the contruction industries. The development goes to prefabricated constructions and to the increased application of construction slabs. These should be as stabile as possible, heat-protecting and noise-protecting but nevertheless they should be lightweighted and having good fire-protecting properties. For this reason in an increasing, extent construction slabs on plaster basis are produced either as plastercard slabs (outside card, inside plaster) or as plasterfiber slabs (for example mixtures of paper fibers and plaster). Plaster has a crystal water proportion of 2 mole and 21% by weight, respectively. Therefore, a certain fire-protection is ensured. However, this fire-protection could be substantially improved with calcium aluminatesalt precipitates having a higher content of water of crystallisation.
A further application field is the production of insulating boards on fiber basis or other insulating materials. They are prepared from pulp, waste paper, waste textiles, coco and other fiber materials by pressing and they have to be made sufficiently fire-protecting by proper additives. As fire-protecting agents useful are mineral materials having a high content of water of crystallisation.
A further possibility for application of calcium aluminate products in the contruction industries is their use as swelling components. In this case calcium aluminates and calcium sulfoaluminates are used the preparation thereof being carried out by sintering raw materials like bauxite, plaster and chalk at very high temperatures of up to 1400° C. This production is very cost and work intensive. An alternative low-cost preparation of swelling components would be highly desired.
Therefore, the object of the invention was to find crystal water-containing calcium compounds which can be easily produced as precipitates in a large scale process and which can be used advantageously in the above-mentioned application fields.
It has been found that this object according to the present invention can be achieved by a process for producing calcium compounds containing water of crystallisation, the process being characterized in that
a) by a chemical reaction between an aqueous alkaline solution of sodium aluminate and a solid or dissolved and suspended, respectively, calcium (hydr)oxide in the presence of carbon dioxide or carbonate a precipitate of a mixture of calcium aluminatehydrates having the following modular formula is formed:
x
CaO.Al
2
O
3
.z
CaCO
3
.y
H
2
O (wherein
x
=3-6
,y
=6-32
,z
=0-1)
and
b) the thus obtained precipitate, in a manner known per se, is separated by sedimentation, dehydrated, optionally washed with water and the thus obtained filter cake is either dried and/or calcined and/or milled,
c) or the filter cake obtained in step (b) in a wet and/or dried form is suspended in water and added with at least one mineral acid and/or at least one salt thereof for forming a calcium aluminatesalt precipitate containing water of crystallisation, the precipitate is separated by sedimentation, dehydrated, optionally washed with water and the thus obtained filter cake is crushed and optionally dried and/or milled.
As an aqueous alkaline sodium aluminate solution preferably a waste pickling lye as obtained in the surface-treatment of aluminum metal with caustic sodium is used.
A particularly preferably used aqueous alkaline sodium aluminate solution and waste pickling lye, respectively, is such one wherein Na
2
O and Al
2
O
3
are present in a mole ratio of (1.0 to 10.0):1, preferably of (1.2 to 2.5):1.
According to a preferred embodiment of the invention in step (a) a diluted caustic sodium is used as the starting material and an alkaline sodium aluminate solution is then added and calcium hydroxide or calcium oxide in solid form or dissolved or suspended in caustic sodium is further added. The order of the addition of the sodium aluminate solution and of the calcium (hydr)oxide can also be reversed.
As calcium compound(s) preferably chalk milk (chalk hydrate or Ca(OH
2
)) or burnt chalk (CaO) is used.
The calcium compound(s) is (are) preferably used in an amount of from 2 to 8 mole of CaO equivalents, in particular from 3 to 5 mole of CaO-equivalents, based on 1 mole of Al
2
O
3
equivalent.
The precipitation of the precipitate in step (a) Is preferably carried out within a reaction time of from 5 to 3000 min, in particular from 60 to 600 min, at a temperature of from 5 to 60° C., preferably from 30 to 50° C. In doing this, a white precipitate of calcium aluminatehydrate containing crystal water is obtained.
According to a
Bings Hubert
Fendel Ansgar
Lehmkuhl Josef
Bos Steven
Rethmann Lippewerk GmbH
Wenderoth Lind & Ponack LLP
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