EP1272427A1 - Method for producing precipitated calcium carbonate - Google Patents
Method for producing precipitated calcium carbonateInfo
- Publication number
- EP1272427A1 EP1272427A1 EP01913859A EP01913859A EP1272427A1 EP 1272427 A1 EP1272427 A1 EP 1272427A1 EP 01913859 A EP01913859 A EP 01913859A EP 01913859 A EP01913859 A EP 01913859A EP 1272427 A1 EP1272427 A1 EP 1272427A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- lime milk
- viscosity
- lime
- milk
- calcium carbonate
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01F—COMPOUNDS OF THE METALS BERYLLIUM, MAGNESIUM, ALUMINIUM, CALCIUM, STRONTIUM, BARIUM, RADIUM, THORIUM, OR OF THE RARE-EARTH METALS
- C01F11/00—Compounds of calcium, strontium, or barium
- C01F11/18—Carbonates
- C01F11/181—Preparation of calcium carbonate by carbonation of aqueous solutions and characterised by control of the carbonation conditions
Definitions
- the invention relates to a process for the preparation of precipitated calcium carbonate (CCP) which is suitable as a functional filler and is distinguished by defined properties.
- CCP precipitated calcium carbonate
- a typical application is its use as a filler in e.g. B. Piastisolen, underbody protection for automobiles, sealants and printing inks.
- the precipitated calcium carbonate is able to control the flow behavior of the masses. For example, by using the appropriate calcium carbonate materials with very different flow behavior.
- the yield point according to Bingham in the plasticizer mixture (SEB) is usually given as a typical characteristic of the application suitability of calcium carbonates as fillers. Depending on the application, high, medium or low flowing grass can be desired.
- the ability of the precipitated calcium carbonate to control the flow limits is influenced, among other things, by the nature of the limestone used for the production of the lime milk, the burning conditions of the limestone and the extinguishing process.
- Finely dispersed calcium carbonate is either made from naturally occurring raw materials by mechanical processing or by chemical means, e.g. B. made by precipitation.
- Precipitated calcium carbonate is usually produced by introducing C0 2 into milk of lime.
- the properties of the precipitated calcium carbonates are e.g. B. depending on the chemical composition of the limestone used, the firing conditions and the extinguishing conditions.
- So-called soft firing is preferably used to produce precipitated calcium carbonate.
- limestone is burned at a temperature of 1,000 to 1,250 ° C.
- the burning process is usually carried out in so-called shaft furnaces or in rotary tube furnaces.
- oil or natural gas can be used as a fuel z. B. coke.
- low firing temperatures lead to high lime milk viscosities.
- the use of this milk of lime for CCP production also leads to small particle diameters of the CCP and high flow limits in the plasticizer mixture. Accordingly, high firing temperatures lead to low lime milk viscosities, coarse CCP particles and low flow limits in the plasticizer mixture.
- the yield of quicklime is highest at medium temperatures, since not all CaC0 3 is converted to CaO at low temperatures and part of the CaO is overburned at high temperatures, ie it can no longer be extinguished using the usual methods.
- the characteristics of quicklime include its ability to react with water.
- the so-called VEC value (Velocite d'Extinction de Chaux).
- the heating rate of a defined water / quicklime mixture is measured.
- Typical VEC values for quicklime, which is suitable for the production of precipitated calcium carbonate, are above 3 ° C / min.
- the quicklime z. B. reacted with water in an extinguishing drum, forming a Ca (OH) 2 suspension, the so-called milk of lime.
- the lime milk usually has a solids content of 70 to 220 g / l of Ca (OH) 2 , a viscosity of 30 to 2500 mPas and an average particle diameter of less than 50 ⁇ m.
- Lime milk is e.g. B. to neutralize. Wastewater, used to make soda or precipitated calcium carbonate.
- the object of the invention is the production of precipitated calcium carbonate (CCP) with controllable defined and reproducible properties in a wide range.
- CCP precipitated calcium carbonate
- the object is achieved in that a lime milk with exactly the viscosity at a given concentration is used for the production of the calcium carbonate with certain rheological properties, which leads to the desired properties of the CCP.
- the properties of calcium carbonate as a rheology-controlling additive are adjusted by the viscosity of the lime milk.
- Piastisoles aim for high flow limits. These are achieved by using lime milk with viscosities above 750 Pas. In print ben medium flow limits are sought so that lime milk with viscosities between 100 and 150 mPas is used for this. For highly filled silicone masses, CCP with a low flow limit are used, so that lime milk with a viscosity below 100 Pas is used.
- the milk of lime thus produced with the viscosity set is then fed to a reactor, into which gas containing CO 2 is introduced to precipitate the calcium carbonate and is homogeneously dispersed in the milk of lime.
- the precipitated calcium carbonate can be post-treated with fatty acids depending on the intended use.
- the precipitation time can be reduced by approximately 20%.
- the viscosity of the milk of lime By adjusting the viscosity of the milk of lime according to the invention, it is possible to significantly influence the flow limit of the CCP-filled plastisols, ie in a targeted manner adjust.
- the yield point was found to be a function of the viscosity of the milk of lime at a given concentration. It was therefore found that the properties of the CCP can be reproducibly influenced by the visually adjustable viscosities of the milk of lime.
- the undesirable influencing of the properties of the CCP by undefined fluctuations in the quality of the limestone of the burning process and the extinguishing process can, for. B. can be canceled by the defined mixing of different limes, the limes being mixed in the ratio from which the desired lime milk viscosity results after subsequent deletion.
- the viscosity can be adjusted by mixing quicklime, which would lead to milk of lime with very different viscosities if used alone, mixed with one another in such a ratio and deleted or deleted together that the desired viscosity of the milk of lime is set. It is also possible to first delete each lime for yourself and then mix the lime milk together. Furthermore, the two limes can be added to the extinguishing apparatus in the specified ratio, where the desired mixture is then formed, from which the desired lime milk viscosity results.
- the measurement of the viscosity of the lime milk is used to control the mixing ratio of the types of lime milk.
- the viscosity is easily z. B. to measure continuously, and via a corresponding control loop, the mixing ratio of the two limes and thus the resulting lime milk quality can be controlled very precisely. Examples 1-6:
- the viscosity of the lime milk can be controlled in a targeted manner by mixing the limes. As a result, the CCP downtime can be reduced by up to 20%.
- the particle diameters of CCP are set reproducibly.
- the flow limit of a mixture of plasticizer and calcium carbonate can be controlled reproducibly.
- the viscosity of the lime milk can also be controlled by grinding the lime milk.
- Known mills can be used to grind the milk of lime. Bead mills are preferably used. Zirconium oxide grinding beads with a diameter of 0.4 to 2 mm are particularly suitable as grinding beads. The fineness of the pearls strongly influences the milling result.
- the grinding effect is also controlled by the speed of the mill, the dwell time of the lime milk in the mill and the resulting specific energy input.
- Solids content 150 g / 1
- the tests are carried out at a constant speed of 1,990 rpm. carried out. Lime milk in the mill was varied. This resulted in various specific energy inputs.
- Limestone is crushed to a grain size of ⁇ 10 mm and then burned for 4 hours at different temperatures. After cooling, the lime is extinguished in a stirred container. This is added to the water in portions. The portions are chosen so that a temperature in the release container does not exceed 95 ° C. A total of 200 g quicklime is added to 1 liter of water. After the reaction is complete, the residue is sieved through a 100 ⁇ sieve and weighed out. The lime milk is diluted to 150 g / 1.
- CCP is produced by introducing gas containing CO into this milk of lime.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Geology (AREA)
- Inorganic Chemistry (AREA)
- Compounds Of Alkaline-Earth Elements, Aluminum Or Rare-Earth Metals (AREA)
Abstract
Description
Claims
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE2000117273 DE10017273A1 (en) | 2000-04-06 | 2000-04-06 | Production of precipitated calcium carbonate comprises controlling the functional properties of the product by controlling the viscosity of the milk of lime |
DE10017273 | 2000-04-06 | ||
PCT/EP2001/002708 WO2001077020A1 (en) | 2000-04-06 | 2001-03-10 | Method for producing precipitated calcium carbonate |
Publications (1)
Publication Number | Publication Date |
---|---|
EP1272427A1 true EP1272427A1 (en) | 2003-01-08 |
Family
ID=7637882
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP01913859A Withdrawn EP1272427A1 (en) | 2000-04-06 | 2001-03-10 | Method for producing precipitated calcium carbonate |
Country Status (5)
Country | Link |
---|---|
EP (1) | EP1272427A1 (en) |
AU (1) | AU2001239288A1 (en) |
DE (1) | DE10017273A1 (en) |
MY (1) | MY136402A (en) |
WO (1) | WO2001077020A1 (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE102007018240A1 (en) * | 2007-04-18 | 2008-10-23 | Voith Patent Gmbh | Process for the formation of calcium carbonate in a pulp suspension |
FI124634B (en) | 2010-06-11 | 2014-11-14 | Upm Kymmene Oyj | Method and apparatus for in-line production of lime milk in a PCC in-line manufacturing process arranged in connection with a fiber web machine |
ES2751144T3 (en) | 2011-10-05 | 2020-03-30 | Imertech Sas | Use of precipitated calcium carbonate particles |
EP2781557A1 (en) | 2013-03-18 | 2014-09-24 | Solvay Sa | Precipitated calcium carbonate, a method for its manufacture and uses thereof |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6086067A (en) * | 1983-10-18 | 1985-05-15 | 奥多摩工業株式会社 | Manufacture of plate-like calcium hydroxide |
JPS62207715A (en) * | 1986-03-08 | 1987-09-12 | Maruo Calcium Kk | Production of calcium carbonate |
JPH0818828B2 (en) * | 1989-12-26 | 1996-02-28 | 奥多摩工業株式会社 | Method for producing agglomerated calcium carbonate |
JP2706384B2 (en) * | 1991-03-22 | 1998-01-28 | 奥多摩工業 株式会社 | Particle size adjustment method of aragonite columnar calcium carbonate |
US5230734A (en) * | 1991-07-29 | 1993-07-27 | Okutama Kogyo Co., Ltd. | Calcium-magnesium carbonate composite and method for the preparation thereof |
DE19900021A1 (en) * | 1999-01-02 | 2000-07-06 | Solvay Soda Deutschland Gmbh | Process for the preparation of precipitated calcium carbonates |
-
2000
- 2000-04-06 DE DE2000117273 patent/DE10017273A1/en not_active Ceased
-
2001
- 2001-03-10 EP EP01913859A patent/EP1272427A1/en not_active Withdrawn
- 2001-03-10 AU AU2001239288A patent/AU2001239288A1/en not_active Abandoned
- 2001-03-10 WO PCT/EP2001/002708 patent/WO2001077020A1/en active Application Filing
- 2001-04-05 MY MYPI20011651 patent/MY136402A/en unknown
Non-Patent Citations (1)
Title |
---|
See references of WO0177020A1 * |
Also Published As
Publication number | Publication date |
---|---|
DE10017273A1 (en) | 2001-10-18 |
AU2001239288A1 (en) | 2001-10-23 |
WO2001077020A1 (en) | 2001-10-18 |
MY136402A (en) | 2008-09-30 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP1016628A1 (en) | Process for the preparation of precipitated calcium carbonate | |
DE602005005979T2 (en) | SURFACE TREATED CALCIUM CARBONATE PARTICLES | |
EP2268863B1 (en) | A pigment particle composition, its method of manufacture and its use | |
EP2150589B1 (en) | Lamp black | |
KR20140031340A (en) | Process for the production of precipitated calcium carbonate, precipitated calcium carbonate and uses thereof | |
EP2141124B1 (en) | Method of producing large-scale and/or nano-scale, coated, disagglomerated magnesium hydroxide particles | |
EP2939980B1 (en) | Production of precipitated calcium carbonate | |
DE69936637T2 (en) | METHOD FOR PRODUCING AND MODIFYING SYNTHETIC CALCIUM CARBONATE | |
DE3617169A1 (en) | CARBONATE-CONTAINING MINERAL FILLERS, PIGMENTS AND SIMILAR MATERIALS | |
DE10311617A1 (en) | Use of at least partly neutralised polyacrylic acid with a mol. wt. of 5000-30000 containing alkylthio end groups, as an auxiliary material for the wet-milling of calcium carbonate | |
DE69105183T2 (en) | Precipitated calcium carbonate. | |
DE102004039664B4 (en) | Flame retardant composition with monomodal particle size distribution based on metal hydroxide and clay, their method of preparation and use, and flame-retardant polymer | |
EP1272427A1 (en) | Method for producing precipitated calcium carbonate | |
CN110366539B (en) | Calcium carbonate and process for producing the same | |
CN107848828B (en) | High solids PCC with depolymerized carboxylated cellulose | |
EP1715009B1 (en) | Use of calcined kaolin for surface coatings, method for its production and calcined kaolin | |
KR910009577B1 (en) | Manufacture of calcitic calcium carbonate | |
JP3668544B2 (en) | Surface-modified heavy calcium carbonate, method for producing the same, and water-based coating composition | |
US20180273395A1 (en) | Production of precipitated calcium carbonate | |
CN107001062B (en) | The improved method for producing winnofil | |
EP0120808A2 (en) | Finely divided calcium carbonate and method of preparing it | |
DE112004002509T5 (en) | Process for hydrometallurgical treatment of steelwork arc electric furnace (EAF) dust and the pigments obtained in this process | |
DE10304314A1 (en) | Production of magnesium hydroxide comprises continuously supplying the reactants to a stirred loop reactor so that hydroxide formation occurs in the presence of a bed of magnesium hydroxide | |
JP2005290059A (en) | Red iron oxide pigment, and coating material and resin composition produced by using the same | |
DE102006005400A1 (en) | Preparing ceramic raw material on the basis of purified aluminum oxide comprises preparing an alumina raw material; calcinating; thermally treating; contacting a bubble-forming carbon dioxide; separating dealklylated alumina; and drying |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
17P | Request for examination filed |
Effective date: 20021106 |
|
AK | Designated contracting states |
Kind code of ref document: A1 Designated state(s): AT BE CH CY DE DK ES FI FR GB GR IE IT LI LU MC NL PT SE TR |
|
AX | Request for extension of the european patent |
Free format text: AL;LT;LV;MK;RO;SI |
|
RAP1 | Party data changed (applicant data changed or rights of an application transferred) |
Owner name: SOLVAY CHEMICALS GMBH |
|
RIN1 | Information on inventor provided before grant (corrected) |
Inventor name: SCHINNINGER, KURT Inventor name: NOVER, CHISTOPH Inventor name: MATTAUSCH, ALFRED Inventor name: DILLENBURG, HELMUT |
|
GRAP | Despatch of communication of intention to grant a patent |
Free format text: ORIGINAL CODE: EPIDOSNIGR1 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN |
|
18D | Application deemed to be withdrawn |
Effective date: 20081001 |