CN1041529C - Process for refining and bleaching barite powder - Google Patents
Process for refining and bleaching barite powder Download PDFInfo
- Publication number
- CN1041529C CN1041529C CN92103253A CN92103253A CN1041529C CN 1041529 C CN1041529 C CN 1041529C CN 92103253 A CN92103253 A CN 92103253A CN 92103253 A CN92103253 A CN 92103253A CN 1041529 C CN1041529 C CN 1041529C
- Authority
- CN
- China
- Prior art keywords
- barite
- powder
- acid
- remove
- water
- 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
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
- C01F11/46—Sulfates
- C01F11/462—Sulfates of Sr or Ba
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)
- Manufacture And Refinement Of Metals (AREA)
- Solid-Sorbent Or Filter-Aiding Compositions (AREA)
Abstract
The present invention provides whole production manufacturing technology for producing industrial filling material of barite powder (ISO3262 barite b grade) by using natural barite mineral resources. The technology is characterized in that barite raw ores are treated by a physical method to obtain micro powder-grade barite superfine raw material which is roasted into clinker under certain conditions. Base is removed by clear water, and dilute acid is used to wash the clinker. After the clinker is pulped, a certain sulphuric acid content and an aluminium powder dosage are controlled. The pulp is stirred to react at boiling temperature to obtain bleached material, and soluble salt is washed by clear water. The bleached material is dried and crushed to obtain a superthin white barite powder finished product. A manufacturer established by the technology of the present invention has low investment for establishing a plant. The present invention has the advantages of low product cost, less energy consumption and low environmental pollution.
Description
The invention relates to a production process for manufacturing a b-grade product of barite according to the international organization for standardization 3262, in particular to a method for micronizing and bleaching barite powder.
The fine barite powder has wide application in the industrial departments of coating, paper making, rubber, printing ink and the like and the medical field. The traditional method for producing barium sulfate powder is a chemical method, the trade name of the product is precipitated barium sulfate, and the product is popular in industrial departments due to good service performance (small particles, low apparent specific gravity and high whiteness). However, the production process of precipitated barium sulfate is very complicated, the production cost is high, and the environmental pollution is difficult to treat, so that the production of ultra-fine barite powder by a physical-chemical method is very important at home and abroad at present. The powder has good dispersibility, high brightness after being prepared into a coating film, long storage period, and can replace a certain proportion of titanium dioxide in a white decorative high-grade coating after being processed to be superfine and high in whiteness.
The invention aims to provide a mineral resource using natural barite. The product produced by the method of the present invention can be used as a filler in industrial departments such as colored paint, rubber, printing ink, plastics, etc., and the product produced by the process of the present invention has the advantages of low cost, less investment in factory building and less environmental pollution.
The purpose of the invention is realized as follows: the method comprises the steps of processing barite raw ore by a physical method to obtain micron-sized barite raw material, and roasting under certain conditions to obtain clinker. Washing with clear water to remove alkalis (discharging and neutralizing the acidic waste water in the method at the same time), washing with dilute acid once, controlling the content of 100 g/l sulfuric acid and the dosage of 0.4% (weight percent) aluminum powder after pulping, and stirring and reacting at the boiling temperature for about 2.5 hours to obtain a bleaching material. Washing with clear water to remove soluble salts. Drying and crushing to obtain the high-fine white barite powder finished product. The specific method comprises the following steps:
1) the barite powder less than 43 microns is obtained after primary crushing of the barite raw ore. The 43 micron powder produced by barite raw ore is always used for drilling oil field, but about 15-20% (weight percentage)<15 micron powder is mixed in 43 micron powder and is detected to be wasted.
2) The grading point is positioned at 15 microns, and the barite powder raw material with the grain size less than 15 microns is obtained by separation through an airflow classifier. This step not only solves the problem of producing a high fine white powder feedstock in a submerged manner, but also improves the quality of the 43 micron powder as a weighting agent for petroleum drilling muds due to the removal of this fine powder (for<43 micron powder).
3) The raw material is roasted in a roasting furnace for 2 to 3 hours at the temperature of 830 ℃ and 890 ℃ to obtain the roasted clinker. The purpose of roasting the raw meal is two: one is to remove free carbon (a main factor influencing whiteness) contained in the raw materials, and the chemical reaction is as follows:
secondly, roasting carbonates, sulphidic minerals such as witherite (BaCO)3) Limestone (CaCO)3) Dolomite ([ Mg, Ca)]CO3) Pyrite (FeS)2) And the like, so that the oxide is converted into oxides which are convenient to process later. The main chemical reaction is as follows: (M represents an alkaline earth metal element)
4) Adding water, stirring and washing. The raw material is calcined to convert the carbonate into oxide. Most of which are soluble in large amounts of water as hydroxides. Through this step, part of impurities contained in the barite raw powder can be removed. And to make it consume no sulfuric acid. The chemical reaction formula is
5) Settling separation removes most of the water. The water separated by settling is strongly alkaline (pH>14). The water and the residual acid water in the subsequent step are discharged simultaneously to reach the sewage discharge standard meeting the regulations of environmental protection departments, thereby realizing environmental protection.
6) Adding diluted acid, stirring and pickling. The dilute acid can be prepared from the waste acid which is press-filtered from the reactor discharge, this step being not critical with respect to the concentration of acid and being essentially the dissolution of the partially insoluble hydroxides, such as, for example, Mg (OH)2. Thus further removing impurities in the raw ore powder.
7) Settling separation removes most of the dilute acid. The dilute acid can be discharged simultaneously with the alkaline water in step 5) to achieve the purpose of neutralization.
8) And (4) pulping, wherein the density (g/cc) d = 1.3-1.8 of the pulp.
9)Pumping the slurry into a reaction kettle, adding sulfuric acid until the content is 100 g/l, adding aluminum powder according to the proportion of 0.4 percent (weight percent) of ore amount by four times, once every 30 minutes and 0.1 percent (weight percent) of each time, and reacting for 2.5 hours at the reaction temperature of 100 +/-5 ℃ to obtain the bleaching material.
10) Discharging and pumping into an acid-resistant filter press for pressure filtration to remove acid liquor. The acid liquor can be returned to the step 6) for use.
11) Washing with water to remove residual acid and iron ions.
12) Most of the water is removed by pressure filtration.
13) Drying on a drying bed and detecting the quality.
14) Crushing, drying and agglomerating to obtain the high-fine white barite powder.
15) And (6) packaging.
The high-fine white barite powder produced by the method can partially or completely replace precipitated barium sulfate and be used in industrial departments of papermaking (partial), paint (partial), plastics (complete), printing ink (complete), rubber (complete) and the like. Meanwhile, the main raw material barite powder adopted by the method is derived from waste materials generated in the process of producing 43-micron barite powder for oil field drilling, the used production equipment is simple and easy to arrange, the production steps are fewer, and the emission in the production process is easy to neutralize or recycle for preparation, so the method also has the advantages of low factory building investment and small environmental pollution. Low product cost, easy popularization and realization in areas with corresponding barite ore resources, and the like.
The process of the invention is further illustrated below with reference to examples:
1) producing 43 micron powder from barite raw ore by a jaw crusher and a Raymond mill;
2) utilizing an FQN-40 type internal circulation airflow classifier (power 3KW) to position a classification point at 15 microns so as to separate fine powder less than 15 microns to obtain a raw material for producing high-fine white barite powder;
3) roasting the raw material in a roasting furnace for 2.5 hours at 870 ℃ to obtain roasted clinker;
4) adding 5-6 times (volume ratio) of water, stirring and washing for 10 minutes;
5) settling and separating out most of water;
6) adding 5-6 times diluted acid (volume ratio), stirring and washing for 10 minutes; the dilute acid can be prepared by using the acid solution obtained by pressure filtering the discharged material from the reaction kettle in step 9);
7) settling and separating to remove most of dilute acid; discharging the alkaline water in step 5) at the same time.
8) Pulping until the pulp density (g/cubic centimeter) d = 1.6;
9) pumping the slurry into a reaction kettle, adding sulfuric acid until the content is 100 g/l, adding aluminum powder (the particle diameter = 0.84 mm) according to 0.4% (weight percent) of the ore amount in four times, stirring and reacting for 2.5 hours at 105 ℃ once every 30 minutes and 0.1% (weight percent) each time to obtain a bleaching material;
10) discharging and pumping into an acid-resistant filter press to remove acid liquor under pressure; the acid solution can be prepared into dilute acid for the step 6).
11) Adding water into the filter press to fully wash out residual acid and soluble salts until no iron ions are detected;
12) press filtering to remove most of water to obtain paste;
13) drying the paste material on a drying bed and detecting various quality indexes;
14) crushing, drying and agglomerating to obtain a finished product of high-fine white barite powder;
15) and (5) bagging the finished product.
Claims (1)
1. A method for micronizing and bleaching barite powder comprises the following steps:
1) primarily crushing barite raw ore to obtain barite powder less than 43 microns;
2) the grading point is positioned at 15 microns, and the barite powder raw material with the grain size less than 15 microns is obtained by separation through an airflow classifier;
3) roasting the raw material in a roasting furnace for 2-3 hours at the temperature of 830-890 ℃ to obtain roasted clinker;
4) adding water, stirring and washing;
5) settling and separating to remove most of water;
6) adding diluted acid, stirring and washing;
7) settling and separating to remove most of dilute acid;
8) beating the slurry to make the density d = 1.3-1.8 g/cc;
9) pumping the slurry into a reaction kettle, adding sulfuric acid until the content is 100 g/l, adding aluminum powder into the reaction kettle four times according to the proportion of 0.4 percent of the ore weight, reacting for 2.5 hours at the reaction temperature of 100 +/-5 ℃ once every 30 minutes and about 0.1 percent of the ore weight at each time, and obtaining a bleaching material;
10) discharging and pumping into an acid-resistant filter press for pressure filtration to remove acid liquor;
11) washing with water to remove residual acid and iron ions;
12) filter pressing to remove most of water;
13) drying on a drying bed and detecting the quality;
14) crushing, drying and agglomerating to obtain a finished product of high-fine white barite powder;
15) and (6) packaging a finished product.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN92103253A CN1041529C (en) | 1992-04-29 | 1992-04-29 | Process for refining and bleaching barite powder |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN92103253A CN1041529C (en) | 1992-04-29 | 1992-04-29 | Process for refining and bleaching barite powder |
Publications (2)
Publication Number | Publication Date |
---|---|
CN1065874A CN1065874A (en) | 1992-11-04 |
CN1041529C true CN1041529C (en) | 1999-01-06 |
Family
ID=4940094
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN92103253A Expired - Fee Related CN1041529C (en) | 1992-04-29 | 1992-04-29 | Process for refining and bleaching barite powder |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN1041529C (en) |
Families Citing this family (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1048998C (en) * | 1994-06-02 | 2000-02-02 | 中国科学院化学研究所 | Porous oxide micro-balls with uniform granule size and preparing method |
CN100375715C (en) * | 2006-06-28 | 2008-03-19 | 上海安亿纳米材料有限公司 | Process for preparing nano barite |
US20080108528A1 (en) * | 2006-11-03 | 2008-05-08 | M-I Llc | Methods to enhance the pneumatic handling characteristics of weighting agents |
CN101941730A (en) * | 2010-08-23 | 2011-01-12 | 郧西华悦矿化有限公司 | Technological method for processing high-gloss barium sulfate |
CN102303890A (en) * | 2011-08-19 | 2012-01-04 | 卢长生 | Production process for converting gray black barite into white barite finished product |
CN102909119A (en) * | 2012-11-06 | 2013-02-06 | 贵州省黄平县江润矿业有限责任公司 | Ultra-fine barite powder processing method |
CN108002420A (en) * | 2016-10-31 | 2018-05-08 | 天柱县晶盛实业有限公司 | A kind of production technology brightened for barite powder |
CN108975375A (en) * | 2018-08-09 | 2018-12-11 | 株洲冶炼集团股份有限公司 | A kind of high whiteness native sulfate of barium production technology of high pure and ultra-fine |
CN108840363A (en) * | 2018-08-09 | 2018-11-20 | 株洲冶炼集团股份有限公司 | A kind of preparation process of high-purity high whiteness barium sulfate |
CN109264762A (en) * | 2018-11-09 | 2019-01-25 | 长沙万荣粉体设备科技有限公司 | A kind of native sulfate of barium method of purification and equipment |
CN109231253A (en) * | 2018-11-09 | 2019-01-18 | 长沙万荣粉体设备科技有限公司 | A kind of native sulfate of barium method of purification and equipment |
CN114213874A (en) * | 2021-12-03 | 2022-03-22 | 贵州民族大学 | Processing method for quality improvement and whitening of barite ore |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1057277A (en) * | 1990-06-11 | 1991-12-25 | 宣化县氧化铁颜料厂 | A kind of production method of ferric oxide red colorant |
-
1992
- 1992-04-29 CN CN92103253A patent/CN1041529C/en not_active Expired - Fee Related
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1057277A (en) * | 1990-06-11 | 1991-12-25 | 宣化县氧化铁颜料厂 | A kind of production method of ferric oxide red colorant |
Also Published As
Publication number | Publication date |
---|---|
CN1065874A (en) | 1992-11-04 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP1482087B1 (en) | A process of recovering alkali from black liquor of papermaking | |
CN1041529C (en) | Process for refining and bleaching barite powder | |
EP0291271B1 (en) | Method of purifying natural calcium carbonate ores | |
RU2583019C2 (en) | High-brightness product for causticising by pre-slaked lime | |
CN1210477A (en) | Method for separating mixture of finely divided minerals | |
CN101050010A (en) | Method for treating acid wastewater of titanium white | |
CN103153863A (en) | Production of calcium carbonate from waste sludge | |
CN1024565C (en) | Comprechensive utilization of serpentine tailings | |
US3616900A (en) | Method for bleaching gray kaolin clay | |
US8545787B2 (en) | Method of treating an aqueous suspension of kaolin | |
US5688315A (en) | Colored titaniferous coating pigment obtained as a flocculated by-product in a kaolin purification process | |
CN1127726A (en) | Method for producing manganese sulfate using waste residue from production of potassium permanganate | |
CN100384728C (en) | Process for production of silica from olivine | |
CN1544535A (en) | Method for purifying and whitening calcium carbonate | |
EP0168492A1 (en) | Method of treating zeolite ores to remove discoloring impurities and improve its brightness and resulting finely ground zeolitic product and coating materials, paper and coated paper containing same. | |
RU2690330C1 (en) | Method for processing slurchen of acid mine water | |
CN1022558C (en) | Method for separating ultrafine iron oxide from waste mother liquor from rutile production by dilute hydrochloric acid | |
CN107021466B (en) | Sulfuric acid method titanium pigment acid waste water is used for the pretreated closed circulation process of phosphorus ore | |
CN1053412A (en) | The bicarbonate of ammonia neutralisation is produced zinc oxide | |
US1680316A (en) | Composite titanium pigment and method of making same | |
CN116639722A (en) | Production and processing technology of barite powder | |
CN115611307A (en) | Preparation method of anatase titanium dioxide special for chemical fibers | |
CN103922363A (en) | Method for preparing 4A zeolite by taking ferrous sulfide tailings as raw materials | |
AU681711B2 (en) | Method for improving the brightness of aluminium hydroxide | |
EP0757971A1 (en) | Process for obtaining a charge of dihydrate calcium sulfate in the form of acicular crystals and utilization in the paper making industry |
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 | ||
C19 | Lapse of patent right due to non-payment of the annual fee | ||
CF01 | Termination of patent right due to non-payment of annual fee |