CN1911801A - Technology for preparating boric acid, magnesium carbonate and sodium sulphate by combined method - Google Patents

Technology for preparating boric acid, magnesium carbonate and sodium sulphate by combined method Download PDF

Info

Publication number
CN1911801A
CN1911801A CN 200610127337 CN200610127337A CN1911801A CN 1911801 A CN1911801 A CN 1911801A CN 200610127337 CN200610127337 CN 200610127337 CN 200610127337 A CN200610127337 A CN 200610127337A CN 1911801 A CN1911801 A CN 1911801A
Authority
CN
China
Prior art keywords
reaction
filtrate
boric acid
magnesium carbonate
magnesium
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.)
Granted
Application number
CN 200610127337
Other languages
Chinese (zh)
Other versions
CN100532259C (en
Inventor
沙文斌
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.)
Individual
Original Assignee
Individual
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 Individual filed Critical Individual
Priority to CNB2006101273374A priority Critical patent/CN100532259C/en
Publication of CN1911801A publication Critical patent/CN1911801A/en
Application granted granted Critical
Publication of CN100532259C publication Critical patent/CN100532259C/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Abstract

The process of co-producing boric acid, magnesium carbonate and sodium sulfate includes the first reaction step of reacting ascharite with 85 % concentration sulfuric acid to obtain wet boric acid and filtering to obtain filtrate; and the second reaction step of reacting the filtrate and sodium carbonate solution inside a reaction pond, filtering to obtain magnesium carbonate, concentrating the filtrate in a directly burning evaporator and hot filtering to obtain anhydrous sodium sulfate.

Description

Combined process for preparing boric acid, magnesium carbonate and sodium sulfate
The technical field is as follows:
the invention relates to the technical field of boron ore processing.
Background
At present, the domestic method for producing boric acid from boron-magnesium ore mainly adopts sulfuric acid to decompose boron-magnesium ore, and after the boric acid is prepared, the boric acid and magnesium sulfate in mother liquor reach a common saturation point. The mother liquor is treated in two ways, namely, the mother liquor is discharged to seriously pollute the environment; and secondly, magnesium sulfate is recovered, but the magnesium sulfate has boric acid, so that the product quality cannot reach the product standard, and the benefit is poor. The process seeks a processing method of the boron-magnesium ore, which can solve the problem of processing the mother liquor in the process and can comprehensively utilize the effective components in the boron-magnesium ore. The final product of the invention obtains boric acid, magnesium carbonate and sodium sulfate. Boric acid is used in the glass industry, enamel and ceramic industry, alkali-free glass fiber industry, metallurgical industry, electrical engineering industry, electroplating, electrolysis industry, pharmaceutical industry, rubber industry, wood preservation, soap manufacturing industry, leather industry, photography, fire-resistant fabrics, synthetic gemstones, dyes, perfume manufacturing, organic synthesis, electrical appliance manufacturing, agriculture, etc., and as a raw material for the production of various boron compounds. Magnesium carbonate is mainly used in rubber industry, dye industry, plastic industry, electronic industry, refractory materials, etc., and is used as a raw material for producing various magnesium compounds and magnesium. The anhydrous sodium sulfate is mainly used as raw material for vinylon, dye, synthetic detergent, glass, paper making, inorganic salt and other industries.
Disclosure of Invention
The method for preparing boric acid by the combined method comprises two steps, namely: after reacting the boron-magnesium ore with sulfuric acid, separating boric acid; the second step of reaction: after boric acid is separated, sodium carbonate is added into the mother liquor for continuous reaction to produce hydrated magnesium carbonate, after the hydrated magnesium carbonate is filtered, the mother liquor is evaporated to separate anhydrous sodium sulfate, and the filtrate is reused.
The first step of reaction:
the second step of reaction:
the process is as follows: the first step of reaction: adding the boron-magnesium ore (fine powder) and 85% sulfuric acid into a reaction tank according to a proportion, wherein the weight ratio of the boron-magnesium ore to the 85% sulfuric acid is 1-3: 0.5-2, adding water, and continuously stirring for reaction at 80-115 ℃. Filtering when the reaction is complete while the reaction is hot, feeding the filtrate into a cooling crystallizer, and cooling and crystallizing under stirring. Separating with a centrifugal separator to obtain wet boric acid, washing, and drying to obtain the final product. And (5) the filtrate enters a second-step reaction tank. The second step of reaction: adding the dissolved sodium carbonate solution into the filtrate obtained in the first step of reaction process, wherein the weight ratio of the boron-magnesium ore to the sodium carbonate is 1-3: 0.5-1, controlling the temperature at 40-70 ℃, and reacting under the condition of continuous stirring. Filtering after the reaction is completed to obtain magnesium carbonate, washing and drying to obtain the finished product. Concentrating the filtrate in a direct combustion evaporator, filtering while the filtrate is hot to obtain anhydrous sodium sulfate product, washing, and drying to obtain the final product. The filtrate is used for the first step of reaction process burdening.
Compared with the traditional one-step method for preparing the boric acid, the process has the advantages that:
1. the problem of low yield of the traditional process is solved, the product yield is improved, and mineral resources are saved;
2. the method is carried out at normal temperature and normal pressure, so that investment, production and management are facilitated, and the operation cost is reduced;
3. the process adopts a direct fuel gas evaporation technology,improves the evaporation efficiency and saves energy;
4. the process has no waste gas and waste water discharge, and is favorable for environmental protection;
5. the waste residue contains boron fertilizer, and can be mixed with phosphate fertilizer to be processed into compound fertilizer;
6. the processing range of the boron-magnesium ore is expanded, and the processing of mineral products with higher magnesium content can be met;
7. the gas source is the self-developed gas producer, and can meet the requirement of fuels in a wider range.
The specific implementation mode is as follows:
the first step of reaction: 2.00 tons of fine powder boron-magnesium ore and 0.75 tons of 85 percent sulfuric acid are added into a reaction tank, water is added, and the mixture is continuously stirred and reacted at 95 ℃. Filtering when the reaction is complete while the reaction is hot, feeding the filtrate into a cooling crystallizer, and cooling and crystallizing under stirring. Separating with a centrifugal separator to obtain wet boric acid, washing, and drying to obtain the final product. And (5) the filtrate enters a second-step reaction tank. The second step of reaction: and adding the dissolved sodium carbonate solution into the filtrate obtained in the first step of reaction process, wherein the amount of the added sodium carbonate is 0.83 ton, the temperature is controlled to be about 55 ℃, and the reaction is carried out under the condition of continuous stirring. Filtering after the reaction is completed to obtain magnesium carbonate, washing and drying to obtain the finished product. And (3) filtering magnesium carbonate, concentrating the filtrate in a direct-fired evaporator, filtering while the filtrate is hot to obtain an anhydroussodium sulfate product, washing and drying to obtain a finished product. The filtrate is used for the first step of reaction process burdening. The resulting product meets the following specifications: boric acid in product specification: GB538-82, hydrated basic magnesium carbonate: HG/T2959-2000 anhydrous sodium sulfate: HG 1-520-80.

Claims (2)

1. A method for preparing boric acid, magnesium carbonate and sodium sulfate is characterized in that: in the first step of reaction, adding fine powder boron-magnesium ore and 85% sulfuric acid into a reaction tank in proportion, adding water, continuously stirring and reacting at 80-115 ℃, filtering while the reaction is complete, feeding the filtrate into a cooling crystallizer, cooling and crystallizing while stirring, separating by using a centrifugal separator to obtain wet boric acid, washing and drying to obtain a finished product; and (2) the filtrate after centrifugal separation enters a second-step reaction tank, in the second-step reaction, the filtrate obtained after the first-step reaction process is added with a dissolved sodium carbonate solution, the temperature is controlled to be 40-70 ℃, the reaction is carried out under continuous stirring, the reaction is completed, the filtrate is filtered to obtain magnesium carbonate, the magnesium carbonate is washed and dried to obtain a finished product, the filtrate obtained after the magnesium carbonate is filtered enters a direct-fired evaporator for concentration, the filtrate is filtered while hot to obtain an anhydrous sodium sulfate product, and the finished product is washed and dried.
2. The method of claim 1, wherein: the weight ratio of the boron-magnesium ore to 85% sulfuric acid is 1-3: 0.5-2, and the weight ratio of the boron-magnesium ore to sodium carbonate is 1-3: 0.5-1.
CNB2006101273374A 2006-09-14 2006-09-14 Technology for preparing boric acid, magnesium carbonate and sodium sulphate by combined method Expired - Fee Related CN100532259C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CNB2006101273374A CN100532259C (en) 2006-09-14 2006-09-14 Technology for preparing boric acid, magnesium carbonate and sodium sulphate by combined method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CNB2006101273374A CN100532259C (en) 2006-09-14 2006-09-14 Technology for preparing boric acid, magnesium carbonate and sodium sulphate by combined method

Publications (2)

Publication Number Publication Date
CN1911801A true CN1911801A (en) 2007-02-14
CN100532259C CN100532259C (en) 2009-08-26

Family

ID=37720900

Family Applications (1)

Application Number Title Priority Date Filing Date
CNB2006101273374A Expired - Fee Related CN100532259C (en) 2006-09-14 2006-09-14 Technology for preparing boric acid, magnesium carbonate and sodium sulphate by combined method

Country Status (1)

Country Link
CN (1) CN100532259C (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101563292B (en) * 2007-12-14 2012-08-29 派诺尔斯管理服务公司 Method for the production of sodium sulphate and magnesium hydroxide
CN108101078A (en) * 2018-01-31 2018-06-01 四川思达能环保科技有限公司 A kind of process system and method with boron magnesium mud production epsom salt

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101563292B (en) * 2007-12-14 2012-08-29 派诺尔斯管理服务公司 Method for the production of sodium sulphate and magnesium hydroxide
CN108101078A (en) * 2018-01-31 2018-06-01 四川思达能环保科技有限公司 A kind of process system and method with boron magnesium mud production epsom salt

Also Published As

Publication number Publication date
CN100532259C (en) 2009-08-26

Similar Documents

Publication Publication Date Title
CN100558633C (en) The method for preparing PHOSPHORIC ACID TECH.GRADE, food grade phosphoric acid and industrial monoammonium phosphate with phosphoric acid by wet process
CN109928872B (en) Method for high-purity synthesis of anthraquinone and co-production of magnesium sulfate
CN110980782A (en) Method for producing high-purity magnesium sulfate by using alkylation waste sulfuric acid and application thereof
CN101492399B (en) Method for preparing methylpropene sodium sulfonate
CN102757072B (en) Process for preparing magnesium sulfate heptahydrate
CN101486481A (en) Method for coproduction of ammonia sulfate and superfine light calcium carbonate from fluorgypsum
CN1911801A (en) Technology for preparating boric acid, magnesium carbonate and sodium sulphate by combined method
CN104445281A (en) Waste residue comprehensive utilization method for trichlorosilane leaching system
CN104557517A (en) Comprehensive treatment process for waste sodium citrate mother solution
CN1063730C (en) Technology for producing magnesium sulfate in treatment of titanium white waste sulfuric acid
CN110304639B (en) Purification method of sodium o-sulfonate benzaldehyde byproduct salt
CN109608354B (en) Method for refining aniline dye intermediate
CN104018397A (en) Paper stiffness improver and preparation method thereof
CN102786076B (en) Method for preparing high-purity copper sulfate by means of waste liquid of copper-contained circuit boards
CN105329952A (en) Refining method of titanium dioxide by-product ferrous sulfate
CN101696016B (en) Hydrothermal synthesis method of alkaline lithium pentaborate
CN109928871B (en) Method for high-purity anthraquinone synthesis and ammonium sulfate co-production
CN111620353A (en) Method for extracting potassium salt from potassium feldspar
CN1202016C (en) Production process of tetrahydrated zirconium sulfate
CN115215310B (en) Impurity removal and recovery method for crude phosphoric acid
CN1215971C (en) Refining method for removing chlorate from perchlorate
CN1114560C (en) Once crystallizing process for rotary separation of boric acid and bitter salt
CN100355719C (en) Salicylic acid preparing process
CN114477249B (en) Method for preparing high-purity magnesium hydroxide and calcium sulfate by adopting calcium carbide furnace purification ash
CN115724453B (en) Purification and recovery method of ferric phosphate mother liquor

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
C17 Cessation of patent right
CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20090826

Termination date: 20100914