CN104418376B - A kind of production technology of winnofil - Google Patents

A kind of production technology of winnofil Download PDF

Info

Publication number
CN104418376B
CN104418376B CN201310394906.1A CN201310394906A CN104418376B CN 104418376 B CN104418376 B CN 104418376B CN 201310394906 A CN201310394906 A CN 201310394906A CN 104418376 B CN104418376 B CN 104418376B
Authority
CN
China
Prior art keywords
carbon dioxide
winnofil
quick lime
digestion reaction
reaction
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.)
Expired - Fee Related
Application number
CN201310394906.1A
Other languages
Chinese (zh)
Other versions
CN104418376A (en
Inventor
武全保
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
JINGXING JINGHUA CALCIUM INDUSTRY Co Ltd
Original Assignee
JINGXING JINGHUA CALCIUM INDUSTRY Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by JINGXING JINGHUA CALCIUM INDUSTRY Co Ltd filed Critical JINGXING JINGHUA CALCIUM INDUSTRY Co Ltd
Priority to CN201310394906.1A priority Critical patent/CN104418376B/en
Publication of CN104418376A publication Critical patent/CN104418376A/en
Application granted granted Critical
Publication of CN104418376B publication Critical patent/CN104418376B/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01FCOMPOUNDS OF THE METALS BERYLLIUM, MAGNESIUM, ALUMINIUM, CALCIUM, STRONTIUM, BARIUM, RADIUM, THORIUM, OR OF THE RARE-EARTH METALS
    • C01F11/00Compounds of calcium, strontium, or barium
    • C01F11/18Carbonates
    • C01F11/181Preparation of calcium carbonate by carbonation of aqueous solutions and characterised by control of the carbonation conditions

Abstract

The present invention proposes the production technology of a kind of winnofil, including: the carbon dioxide produced during limestone calcination is removed, chaotropic agent is added before digestion reaction, dispersant is added during digestion reaction, carry out digestion reaction with quick lime and water and prepare slaked lime, supplement carbon dioxide during slaked lime carburizing reagent, reclaim and obtain product.The production technology of winnofil of the present invention, the problem that in production process, reaction rate is relatively slow, energy consumption is bigger is solved by controlling the concentration of carbon dioxide in production process, improve the production efficiency of winnofil, reduce energy consumption, save production cost, it is easy to accomplish industrialized production.

Description

A kind of production technology of winnofil
Technical field
The present invention relates to the production technology of winnofil, particularly relate to a kind of by controlling carbon dioxide Concentration improves reaction rate, reduces the production technology of the winnofil of energy consumption of reaction.
Background technology
Winnofil is a kind of critically important inorganic chemical product, and tool has been widely used, and such as it is by extensively Generally as the functional filler of material, such as pigment, papermaking, coating, ink, plastics or sealant etc.. Other application of winnofil are included in the industry such as food, cosmetics and medicine.
The classical production technology feature description of winnofil is as follows: limestone divides through calcining furnace calcination reaction Solution becomes quick lime and carbon dioxide;Quick lime obtains slaked lime through water digestion reaction, i.e. calcium hydroxide Emulsion;Carbon dioxide and slaked lime are carried out carburizing reagent under certain control condition and must precipitate carbonic acid Calcium.The winnofil produced through being dehydrated, be dried, pulverize and packaging becomes finished product winnofil.
Above-mentioned relevant chemical equation is:
Limestone calcination reaction CaCO3→CaO+CO2
Quicklime slaking reaction CaO+H2O→Ca(OH)2
Slaked lime carburizing reagent Ca (OH)2+CO2→CaCO3+H2O
Wherein, in actual production, calcining furnace height is higher, may be up to 25 meters, how to control calcining furnace Reaction rate is problems faced during winnofil produces.Have at present and temperature sensor is set in calcining furnace Measure solve the problems referred to above, according to temperature sensor transmission temperature data control aerator power, This method also can on certain extent control reaction rate, but installation difficulty is relatively big, cost is the highest. In the carbonisation of slaked lime, the carbon dioxide produced in calcining furnace is passed through through washing and compression In carbonators, because the slaked lime that first carburizing reagent is dissolved in water generates carbonic acid with carbon dioxide Calcium, then solid phase adds to rapidly make to be swift in response in liquid phase go on.But in process of production, due to Ca(OH)2Having the least dissolubility in water, carburizing reagent speed is slow, needs to use powerful aerator Constantly toward transport of carbon dioxide in carbonators, this is whole winnofil energy consumption the best part, consumes The substantial amounts of energy.Above-mentioned factor causes whole winnofil production process relatively slow, relatively costly.
Summary of the invention
The present invention proposes the production technology of a kind of winnofil, solves in prior art anti-in production process Answer speed relatively slow, the problem that energy consumption is bigger.
The invention provides the production technology of a kind of winnofil, comprise the following steps:
1) being loaded by limestone in calcining furnace and calcine, blast rate is 3.0~7.5m3/ h, removes carbon dioxide Gas, the density of carbon dioxide gas controlled in calcining furnace is 5%~10%, obtains quick lime;
2) step 1) gained quick lime is carried out digestion reaction in digester, obtain slaked lime;
3) by step 2) gained slaked lime carries out carburizing reagent in carbonators, and blast rate is 5.0~9.0 m3/ h, the density of carbon dioxide gas controlled in carbonators is 20%~80%, keeps the pH of product mixtures Value at least 9.5;And
4) winnofil is reclaimed.
Preferably, the chaotropic agent of 0.3%~the 2.4% of addition quick lime weight ratio before digestion reaction starts;Digestion Reaction adds the dispersant of 0.5%~the 3% of quick lime weight ratio after starting 10min.
Preferably, the chaotropic agent of 1.2%~the 2.0% of addition quick lime weight ratio before digestion reaction starts;Digestion Reaction adds the dispersant of 1.5%~the 2.5% of quick lime weight ratio after starting 10min.
Preferably, at least one during chaotropic agent is sorbitol, ethylene glycol heteroside, mannitol, glycerol; Dispersant is acrylic acid, methacrylic acid, itaconic acid, maleic acid, 2-(Acryloyloxy)ethanol, methacrylic acid At least one in hydroxypropyl acrylate, ammonium acetate, ammonium formate.
Preferably, in step 1) in, exist from calcination reaction first stage turning to calcination reaction second stage Becoming, the feature of transformation is the speed decline that reactant mixture produces carbon dioxide, wherein, the two of generation 80%~the 90% of stoichiometric total amount of carbon oxide gas removes in the first phase, and remainder is Two-stage removes.
Preferably, in step 3) in, exist from carburizing reagent first stage turning to carburizing reagent second stage Becoming, the feature of transformation is that the speed of reactant mixture absorbing carbon dioxide gas declines, wherein, and carbon dioxide 70%~the 80% of stoichiometric total amount of gas disperses in the first phase, and remainder is in second stage Middle dispersion.
Preferably, in step 3) in the carburizing reagent first stage, carbon dioxide is can be mixed by reaction The maximum rate dispersion that thing absorbs.
Preferably, in step 3) in carburizing reagent second stage, carbon dioxide is can be mixed by reaction The maximum rate dispersion that thing absorbs, in carburizing reagent second stage, the dispersion rate of carbon dioxide is less than carbon Change the dispersion rate of carbon dioxide in the reaction first stage.
Preferably, the pH value of product mixtures is at least 10.0.
According to the feature of reaction involved by the production technology of winnofil, in the calcination reaction first stage, produce The speed of raw carbon dioxide is relatively fast, adjusts relatively fast blast rate and enters to remove carbon dioxide And gas concentration lwevel is at reduced levels in controlling calcining furnace.By the particular point in time depending on reaction condition it After, the calcination reaction first stage changes to calcination reaction second stage, mixed in the reaction of calcination reaction second stage Compound produces the maximum rate of carbon dioxide and produces carbon dioxide less than the calcination reaction first stage Maximum rate.Condition is asked, during the transformation in above-mentioned two stage, due to carbon dioxide gas according to reaction Body produces the reduction of speed, and calcining in-furnace temperature may relative constancy.
In a preferred embodiment of the invention, in carbonation reaction, first stage carbon dioxide is divided The speed being scattered in reactant mixture is maximum rate, can be absorbed at above-mentioned speed carbon dioxide gas, So seldom discharge from reactant mixture even without carbon dioxide, and then by carburizing reagent Time necessary to one stage shortens to minimum, thus improves the throughput rate of whole process.
In like manner, carburizing reagent second stage also preferably uses the maximum dioxy that can be absorbed by reactant mixture Changing carbon dispersion rate to carry out, the most above-mentioned stage has the formation of slaked lime solution state.Generally carbon Change the reaction second stage speed first stage to be less than.
Preferably, for guaranteeing that the excess of carbon dioxide causes the decline of winnofil yield, control to produce The pH value of thing mixture, its size is at least 10.0.
When digestion reaction, in sorbitol, ethylene glycol heteroside, mannitol or glycerol, at least one deposits Under, it is possible to making the calcium ion being dissolved in reaction system increase, the amount of addition is the most, the calcium ion of dissolving Amount increases the most.During digestion reaction, acrylic acid, methacrylic acid, itaconic acid, maleic acid, third In olefin(e) acid hydroxyl ethyl ester, Hydroxypropyl methacrylate, ammonium acetate or ammonium formate in the presence of at least one, it is possible to Accelerate the dispersion rate of reactant, the in addition adjustment of reaction system stir speed (S.S.) and the control of blast rate, all The dispersion rate of carbon dioxide can be improved, and then improve throughput rate.
The production technology of a kind of winnofil of the present invention, begins to be controlled from limestone calcination Density of carbon dioxide gas, quicklime slaking reaction before addition chaotropic agent sorbitol, ethylene glycol heteroside, Mannitol or glycerol, during digestion reaction add dispersant acrylic acid, methacrylic acid, itaconic acid, Maleic acid, 2-(Acryloyloxy)ethanol, Hydroxypropyl methacrylate, ammonium acetate or ammonium formate, produced by control During the concentration of carbon dioxide improve the carbonation rate of the decomposition rate of limestone, slaked lime, solve The problem that in production process winnofil reaction rate is slow, energy consumption is high, can be real with conventional equipment Now produce, production cost reduce, simple to operate, it is easy to accomplish industrialized production, can promote industrialization should With.
Accompanying drawing explanation
Fig. 1 is the production technological process of a kind of winnofil of the present invention.
Detailed description of the invention
Below in conjunction with the accompanying drawing in the embodiment of the present invention, the technical scheme in the embodiment of the present invention is carried out clearly Chu, be fully described by, it is clear that described embodiment be only a part of embodiment of the present invention rather than Whole embodiments.Based on the embodiment in the present invention, those of ordinary skill in the art are not making creation The every other embodiment obtained under property work premise, broadly falls into the scope of protection of the invention.
Embodiment 1:
1) 6 tons of limestone loading calcining in calcining furnace, blast rate is 5.5m3/ h, removes carbon dioxide Gas, the density of carbon dioxide gas controlled in calcining furnace is 8%, obtains quick lime;
2) step 1) gained quick lime is carried out digestion reaction in digester, obtain slaked lime;
3) by step 2) gained slaked lime carries out carburizing reagent in carbonators, and blast rate is 7.0m3/ h, The density of carbon dioxide gas controlled in carbonators is 50%, keeps the pH value of product mixtures to be at least 9.5; And
4) winnofil is reclaimed.
The time-consuming 3.5h of calcination reaction in production process, the time-consuming 3.2h of carburizing reagent, relative to not controlling titanium dioxide The time of the classical production technology that carbon gas concentration, remaining reaction condition are identical shortens about 25%, thus drops Low energy consumption.
Embodiment 2
1) 6 tons of limestone loading calcining in calcining furnace, blast rate is 5.5m3/ h, removes carbon dioxide Gas, the density of carbon dioxide gas controlled in calcining furnace is 8%, carbon dioxide stoichiometric always The 80% of amount removes in the first phase, and remainder removes in second stage, obtains quick lime;
2) step 1) gained quick lime being carried out in digester digestion reaction, digestion reaction starts front addition The sorbitol of the 0.3% of quick lime weight ratio;Digestion reaction adds the 0.5% of quick lime weight after starting 10min Acrylic acid, obtain slaked lime;
3) by step 2) gained slaked lime carries out carburizing reagent, the chemistry of carbon dioxide in carbonators The 70% of the total amount of equivalent disperses in the first phase, and remainder disperses in second stage, blast rate For 7.0m3/ h, the density of carbon dioxide gas controlled in carbonators is 50%, keeps the pH of product mixtures Value at least 9.5;And
4) winnofil is reclaimed.
The time-consuming 3.5h of calcination reaction in production process, the time-consuming 2.8h of carburizing reagent, relative to not controlling titanium dioxide The time of the classical production technology that carbon gas concentration, remaining reaction condition are identical shortens about 25%, thus drops Low energy consumption.
Embodiment 3
1) 6 tons of limestone loading calcining in calcining furnace, blast rate is 5.5m3/ h, removes carbon dioxide Gas, the density of carbon dioxide gas controlled in calcining furnace is 8%, carbon dioxide stoichiometric always The 90% of amount removes in the first phase, and remainder removes in second stage, obtains quick lime;
2) step 1) gained quick lime being carried out in digester digestion reaction, digestion reaction starts front addition The Glycol glycoside of the 2.4% of quick lime weight ratio;Digestion reaction adds quick lime weight after starting 10min The itaconic acid of 3%, obtains slaked lime;
3) by step 2) gained slaked lime carries out carburizing reagent, the chemistry of carbon dioxide in carbonators The 80% of the total amount of equivalent disperses in the first phase, and remainder disperses in second stage, blast rate For 7.0m3/ h, the density of carbon dioxide gas controlled in carbonators is 50%, keeps the pH of product mixtures Value at least 9.5;And
4) winnofil is reclaimed.
The time-consuming 3.5h of calcination reaction in production process, the time-consuming 2.7h of carburizing reagent, relative to not controlling titanium dioxide The time of the classical production technology that carbon gas concentration, remaining reaction condition are identical shortens about 25%, thus drops Low energy consumption.
Embodiment 4
1) 6 tons of limestone loading calcining in calcining furnace, blast rate is 5.5m3/ h, removes carbon dioxide Gas, the density of carbon dioxide gas controlled in calcining furnace is 8%, carbon dioxide stoichiometric always The 80% of amount removes in the first phase, and remainder removes in second stage, obtains quick lime;
2) step 1) gained quick lime being carried out in digester digestion reaction, digestion reaction starts front addition The glycerol of the 1.2% of quick lime weight ratio;Digestion reaction adds the 2.5% of quick lime weight after starting 10min Maleic acid, obtain slaked lime;
3) by step 2) gained slaked lime carries out carburizing reagent, the chemistry of carbon dioxide in carbonators The 70% of the total amount of equivalent disperses in the first phase, and remainder disperses in second stage, blast rate For 7.0m3/ h, the density of carbon dioxide gas controlled in carbonators is 50%, keeps the pH of product mixtures Value at least 9.5;And
4) winnofil is reclaimed.
The time-consuming 3.5h of calcination reaction in production process, the time-consuming 2.5h of carburizing reagent, relative to not controlling titanium dioxide The time of the classical production technology that carbon gas concentration, remaining reaction condition are identical shortens about 30%, thus drops Low energy consumption.
Embodiment 5
1) 6 tons of limestone loading calcining in calcining furnace, blast rate is 5.5m3/ h, removes carbon dioxide Gas, the density of carbon dioxide gas controlled in calcining furnace is 8%, carbon dioxide stoichiometric always The 90% of amount removes in the first phase, and remainder removes in second stage, obtains quick lime;
2) step 1) gained quick lime being carried out in digester digestion reaction, digestion reaction starts front addition The mannitol of the 2.0% of quick lime weight ratio;Digestion reaction adds the 1.5% of quick lime weight after starting 10min Ammonium acetate, obtain slaked lime;
3) by step 2) gained slaked lime carries out carburizing reagent, the chemistry of carbon dioxide in carbonators The 70% of the total amount of equivalent disperses in the first phase, and remainder disperses in second stage, blast rate For 7.0m3/ h, the density of carbon dioxide gas controlled in carbonators is 50%, keeps the pH of product mixtures Value at least 9.5;And
4) winnofil is reclaimed.
The time-consuming 3.5h of calcination reaction in production process, the time-consuming 2.4h of carburizing reagent, relative to not controlling titanium dioxide The time of the classical production technology that carbon gas concentration, remaining reaction condition are identical shortens about 30%, thus drops Low energy consumption.
Embodiment 6
1) 6 tons of limestone loading calcining in calcining furnace, blast rate is 3.0m3/ h, removes carbon dioxide Gas, the density of carbon dioxide gas controlled in calcining furnace is 10%, carbon dioxide stoichiometric The 80% of total amount removes in the first phase, and remainder removes in second stage, obtains quick lime;
2) step 1) gained quick lime being carried out in digester digestion reaction, digestion reaction starts front addition The sorbitol of the 0.3% of quick lime weight ratio;Digestion reaction adds the 0.5% of quick lime weight after starting 10min Methacrylic acid, obtain slaked lime;
3) by step 2) gained slaked lime carries out carburizing reagent, the chemistry of carbon dioxide in carbonators The 70% of the total amount of equivalent disperses in the first phase, and remainder disperses in second stage, blast rate For 5.0m3/ h, the density of carbon dioxide gas controlled in carbonators is 20%, keeps the pH of product mixtures Value at least 9.5;And
4) winnofil is reclaimed.
The time-consuming 4.0h of calcination reaction in production process, the time-consuming 2.2h of carburizing reagent, relative to not controlling titanium dioxide The time of the classical production technology that carbon gas concentration, remaining reaction condition are identical shortens about 30%, thus drops Low energy consumption.
Embodiment 7
1) 6 tons of limestone loading calcining in calcining furnace, blast rate is 7.5m3/ h, removes carbon dioxide Gas, the density of carbon dioxide gas controlled in calcining furnace is 5%, carbon dioxide stoichiometric always The 80% of amount removes in the first phase, and remainder removes in second stage, obtains quick lime;
2) step 1) gained quick lime being carried out in digester digestion reaction, digestion reaction starts front addition The sorbitol of the 1.5% of quick lime weight ratio;Digestion reaction adds the 2.5% of quick lime weight after starting 10min 2-(Acryloyloxy)ethanol, obtain slaked lime;
3) by step 2) gained slaked lime carries out carburizing reagent, the chemistry of carbon dioxide in carbonators The 80% of the total amount of equivalent disperses in the first phase, and remainder disperses in second stage, blast rate For 9.0m3/ h, the density of carbon dioxide gas controlled in carbonators is 80%, keeps the pH of product mixtures Value at least 9.5;And
4) winnofil is reclaimed.
The time-consuming 3.0h of calcination reaction in production process, the time-consuming 2.0h of carburizing reagent, relative to not controlling titanium dioxide The time of the classical production technology that carbon gas concentration, remaining reaction condition are identical shortens about 35%, thus drops Low energy consumption.
Embodiment 8
1) 8 tons of limestone loading calcining in calcining furnace, blast rate is 7.0m3/ h, removes carbon dioxide Gas, the density of carbon dioxide gas controlled in calcining furnace is 10%, carbon dioxide stoichiometric The 90% of total amount removes in the first phase, and remainder removes in second stage, obtains quick lime;
2) step 1) gained quick lime being carried out in digester digestion reaction, digestion reaction starts front addition The glycol glucoside of the 2.0% of quick lime weight ratio;Digestion reaction adds quick lime weight after starting 10min 1.5% ammonium formate, obtain slaked lime;
3) by step 2) gained slaked lime carries out carburizing reagent, the chemistry of carbon dioxide in carbonators The 70% of the total amount of equivalent disperses in the first phase, and remainder disperses in second stage, blast rate For 8.5m3/ h, the density of carbon dioxide gas controlled in carbonators is 75%, keeps the pH of product mixtures Value at least 10.0;And
4) winnofil is reclaimed.
The time-consuming 3.0h of calcination reaction in production process, the time-consuming 2.2h of carburizing reagent, relative to not controlling titanium dioxide The time of the classical production technology that carbon gas concentration, remaining reaction condition are identical shortens about 35%, thus drops Low energy consumption.
The foregoing is only presently preferred embodiments of the present invention, not in order to limit the present invention, all at this Within bright spirit and principle, any modification, equivalent substitution and improvement etc. made, should be included in this Within bright protection domain.

Claims (4)

1. the production technology of a winnofil, it is characterised in that: comprise the following steps,
1) being loaded by limestone in calcining furnace and calcine, blast rate is 3.0~7.5m3/ h, removes the two of generation Carbon oxide gas, the density of carbon dioxide gas controlled in calcining furnace is 5%~10%, obtains quick lime;
2) by step 1) gained quick lime carries out digestion reaction in digester, obtains slaked lime;
3) by step 2) gained slaked lime carries out carburizing reagent in carbonators, and blast rate is 5.0~9.0 m3/ h, the density of carbon dioxide gas controlled in carbonators is 20%~80%, keeps the pH of product mixtures Value at least 9.5;And
4) winnofil is reclaimed;
Described digestion reaction adds the chaotropic agent of 0.3%~the 2.4% of quick lime weight ratio before starting;Described digestion Reaction adds the dispersant of 0.5%~the 3% of quick lime weight ratio after starting 10min;
Described chaotropic agent is at least one in sorbitol, mannitol or glycerol;Described dispersant is propylene Acid, methacrylic acid, itaconic acid, maleic acid, 2-(Acryloyloxy)ethanol, Hydroxypropyl methacrylate, acetic acid At least one in ammonium or ammonium formate.
The production technology of a kind of winnofil the most according to claim 1, it is characterised in that described Digestion reaction adds the chaotropic agent of 1.2%~the 2.0% of quick lime weight ratio before starting;Described digestion reaction starts The dispersant of 1.5%~the 2.5% of addition quick lime weight ratio after 10min.
The production technology of a kind of winnofil the most according to claim 1, it is characterised in that in step Rapid 1), in, exist from the calcination reaction first stage to the transformation of calcination reaction second stage, the spy of described transformation Levy be reactant mixture produce carbon dioxide speed decline, wherein, the carbon dioxide of generation 80%~the 90% of the total amount of equivalent removes in the first phase, and remainder removes in second stage.
The production technology of a kind of winnofil the most according to claim 1, it is characterised in that described product The pH value of thing mixture is at least 10.0.
CN201310394906.1A 2013-09-03 2013-09-03 A kind of production technology of winnofil Expired - Fee Related CN104418376B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201310394906.1A CN104418376B (en) 2013-09-03 2013-09-03 A kind of production technology of winnofil

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201310394906.1A CN104418376B (en) 2013-09-03 2013-09-03 A kind of production technology of winnofil

Publications (2)

Publication Number Publication Date
CN104418376A CN104418376A (en) 2015-03-18
CN104418376B true CN104418376B (en) 2016-08-17

Family

ID=52968606

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201310394906.1A Expired - Fee Related CN104418376B (en) 2013-09-03 2013-09-03 A kind of production technology of winnofil

Country Status (1)

Country Link
CN (1) CN104418376B (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109467113A (en) * 2019-01-16 2019-03-15 连平县鑫福建材有限公司 A kind of production technology of calcium carbonate powder

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109133137B (en) * 2018-11-14 2020-12-08 上海应用技术大学 Ellipsoidal micro-nano calcium carbonate and preparation method thereof
CN114276698B (en) * 2021-12-30 2023-04-07 广西华纳新材料股份有限公司 Preparation method of nano calcium carbonate for nail-free glue

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102674425A (en) * 2012-05-19 2012-09-19 祁阳建明化工有限责任公司 Production technique of nano calcium carbonate by normal temperature method
CN102757074A (en) * 2011-04-25 2012-10-31 琳德股份公司 Method and system for preparing precipitate calcium carbonate

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB0917248D0 (en) * 2009-10-02 2009-11-18 Calcitech Synthetic Minerals Ltd Production of calcium carbonate

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102757074A (en) * 2011-04-25 2012-10-31 琳德股份公司 Method and system for preparing precipitate calcium carbonate
CN102674425A (en) * 2012-05-19 2012-09-19 祁阳建明化工有限责任公司 Production technique of nano calcium carbonate by normal temperature method

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109467113A (en) * 2019-01-16 2019-03-15 连平县鑫福建材有限公司 A kind of production technology of calcium carbonate powder

Also Published As

Publication number Publication date
CN104418376A (en) 2015-03-18

Similar Documents

Publication Publication Date Title
EP2371766B1 (en) Process for obtaining precipitated calcium carbonate
CN102602973B (en) Method for synthesizing ultrafine calcium carbonate by utilizing carbide slag
RU2436734C2 (en) Method of producing precipitated calcium carbonate, method of increasing content of dry substance of precipitated calcium carbonate product and reactor system for producing precipitated calcium carbonate
CN101293663B (en) Novel technique for preparing fine calcium carbonate
CN102757075B (en) Method for preparing calcium carbonate powders of different structures and shapes
US20120082602A1 (en) METHOD FOR INDUSTRIAL MANUFACTURE OF PRECIPITATED CALCIUM CARBONATE (CaCO3) FROM CARBONATE BEARING ROCKS
CN104418376B (en) A kind of production technology of winnofil
EP3060523A1 (en) Process and apparatus for manufacture of hydroxide slurry
CN103170226A (en) New process for fixing carbon dioxide
CN112573555A (en) Carbide slag mineralization fixation of CO2And method for preparing fine calcium carbonate
JP2012529418A (en) Method for producing calcium carbonate
US7326400B2 (en) Treatment of high sulfate containing quicklime
CN101804998B (en) Method for producing high-purity magnesium oxide by using dolomite
KR101831971B1 (en) Preparing method for complex calcium carbonate using coal ash
CN109437261A (en) A kind of sheeted nanometer magnesium hydroxide raw powder's production technology
CN103172100A (en) Method for preparing calcium carbonate in different grain sizes
CN108793217A (en) The preparation method of one bulb tufted shape precipitated calcium carbonate
CN110563007A (en) Method for converting sodium sulfate into sodium bicarbonate by using calcium oxide and carbon dioxide
CN107445188B (en) A kind of preparation method of rod-like precipitates calcium carbonate
CN101214979A (en) Method for synthesizing active magnesium hydroxide
CN102838141A (en) Process for producing magnesium hydrate by removing silicon and aluminum from magnesite
CN101920981A (en) Material recycling method for producing calcium carbonate by ammonium carbonization method
CN109467113A (en) A kind of production technology of calcium carbonate powder
CN110589866B (en) Method for preparing ultrafine powder vaterite by using steel slag
CN116528963A (en) Method for producing calcium carbonate and calcium carbonate

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant
CF01 Termination of patent right due to non-payment of annual fee
CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20160817

Termination date: 20180903