CN1974388A - Sodium carbonate preparing process - Google Patents

Sodium carbonate preparing process Download PDF

Info

Publication number
CN1974388A
CN1974388A CNA2006101353364A CN200610135336A CN1974388A CN 1974388 A CN1974388 A CN 1974388A CN A2006101353364 A CNA2006101353364 A CN A2006101353364A CN 200610135336 A CN200610135336 A CN 200610135336A CN 1974388 A CN1974388 A CN 1974388A
Authority
CN
China
Prior art keywords
ammonia
nio
water vapor
soda ash
mixture
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
CNA2006101353364A
Other languages
Chinese (zh)
Other versions
CN100436322C (en
Inventor
钟劲光
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.)
Zhongke Yigong Shanghai Chemical Technology Co ltd
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 CNB2006101353364A priority Critical patent/CN100436322C/en
Publication of CN1974388A publication Critical patent/CN1974388A/en
Application granted granted Critical
Publication of CN100436322C publication Critical patent/CN100436322C/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/141Feedstock

Landscapes

  • Manufacture And Refinement Of Metals (AREA)
  • Processing Of Solid Wastes (AREA)
  • Fertilizers (AREA)

Abstract

The present invention is ammonia-nickel process for preparing sodium carbonate, and the process has facile material, low medium ammonia and nickel loss, reuse of medium ammonia and nickel, less pollutant exhaustion and high product quality with chlorine content controlled within 0.1 %. The preparation process includes the following steps: dissolving NiO in the mixture solution of CO2 and ammonia to absorb ammonia to saturation, adding NaCl for metathesis, filtering to separate ammonia water solution of Na2CO3 and Ni(NH3)6Cl2, distilling ammonia water solution of Na2CO3 to eliminate ammonia, filtering to obtain precipitate Ni2(OH)2CO3, concentrating the filtrate to crystallize sodium carbonate product, heating Ni(NH3)6Cl2 to eliminate ammonia and obtain NiCl2, heating NiCl2 to react with water vapor to obtain NiO and mixture of HCl and water vapor, recovering NiO, condensating the mixture of HCl and water vapor to obtain hydrochloric acid and mixing Cl2 and air to obtain liquid chlorine.

Description

Preparation method of sodium carbonate
Technical Field
The invention relates to a carbonate of sodium, potassium or general alkalimetal, in particular to a process for preparing calcined soda by adopting an ammonia nickel method.
Background
The traditional alkali making process mainly comprises an ammonia-soda process, a combined-soda process and a natural alkali refining process, wherein the ammonia-soda process has the advantages of easily obtained raw materials, mature and simple process, low utilization rate of NaCl and simultaneously generation of a large amount of waste liquid. The combined alkali method solves the problems existing in the ammonia-soda method, but has higher equipment requirement and by-product NH4Cl as a fertilizerIs limited abroad, is limited by the market price of other nitrogen fertilizers at home, and has low added value.
Plum loyalty in the invention patent application with publication number CN1308020 provides a new soda production process by adding CaCl in ammonia distillation mother liquor2And converting into CaO again, and returning to the ammonia distillation system. So as to thoroughly eliminate a large amount of waste liquid and waste residue in the ammonia-soda process soda production and reduce the consumption. The theory is as follows:
xugui in the invention patent application with publication No. CN1814548 provides a process for producing soda by ammonia-soda process without waste discharge, which is to treat the waste residue liquid from the ammonia evaporation process, separate the waste residue liquid by the separation process to remove the slag and wash the slag to obtain the engineering soil product; reacting the supernatant with frozen nitre (Na2SO4) in a reaction process to obtain a refined gypsum product; the circulating liquid from the reaction process enters a brine process for recycling; and the redundant circulating liquid enters a salt making procedure to prepare a refined salt product.
Disclosure of Invention
The invention aims to solve the problems of the existing alkali making process and provide a method for preparing sodium carbonate, which has the advantages of easily available raw materials, low loss of medium ammonia and nickel, cyclic utilization, no waste generation in the middle, low discharge capacity, high quality of prepared target products and controllable chlorine content within 0.1%.
The technical scheme of the invention is that NaCl and industrial CO are used2Water and air as raw materials, and ammonia and nickel as media to prepare soda ash and hydrochloric acid or chlorine.
The invention comprises the following steps:
1) dissolving NiO in CO2Adding ammonia into the mixed solution of the sodium chloride and ammonia water, absorbing ammonia until the mixed solution is saturated, adding NaCl for double decomposition, filtering and separating Na2CO3Aqueous ammonia solution and Ni (NH)3)6Cl2
2) Mixing Na2CO3Distilling ammonia water solution to remove ammonia, filtering out precipitate Ni2(OH)2CO3Concentrating and crystallizing the filtrate to obtain a soda ash product;
3) mixing Ni (NH)3)6Cl2Heating to 150-200 ℃ and deaminizing to obtain NiCl2
4) Mixing NiCl2Heating to 500-1000 ℃, reacting with water vapor to obtain NiO and a mixture of hydrogen chloride and water vapor, or reacting with O in the air2Reacting to obtain NiO and Cl2Mixing with air, recovering NiO to the leaching step in step 1 for recycling, and condensing the mixture of hydrogen chloride and water vapor to obtain hydrochloric acid product, Cl2The mixed gas with air is separated into liquid chlorine product by freezing.
NiO and CO in a mass ratio2∶NaCl=100∶62∶162,NiCl2100: 200 of water vapor.
The basic principle of the invention is as follows: because NiO is easily dissolved in (NH)4)2CO3Solution, Ni (NH) can be easily formed3)6CO3Solution of Ni (NH)3)6Cl2The solubility in concentrated ammonia is very low, so that the above characteristics are utilized, and NaCl and Ni (NH) are used3)6Cl2Carrying out double decomposition reaction to obtain Na2CO3The chemical reaction formula is as follows:
Figure A20061013533600042
wherein ammonia and nickel are recycled, and theoretically, the loss in the process is very small.
The invention solves the problems in the existing ammonia-soda process for preparing the sodium carbonate, the needed raw materials are easy to obtain, the loss of medium ammonia and nickel is small, the medium ammonia and nickel can be recycled, no waste is generated in the middle, the discharge capacity is small, the chlorine content of the prepared target product low-chlorine sodium carbonate is less than 0.1 percent, and the byproduct is hydrochloric acid or chlorine.
Detailed Description
The following examples further illustrate the invention.
10kgNiO was dissolved in a solution containing 6.2kgCO2CO of2Adding into mixed solution of ammonia water, absorbing ammonia until saturation, adding 16.2kg NaCl for double decomposition, filtering, and separating Na2CO3Aqueous ammonia solution and Ni (NH)3)6Cl2(ii) a Mixing Na2CO3Distilling ammonia water solution to remove ammonia, filtering out precipitate Ni2(OH)2CO3Concentrating and crystallizing the filtrate to obtain a soda ash product; mixing Ni (NH)3)6Cl2Heating to 150-200 ℃ and deaminizing to obtain NiCl2(ii) a Mixing NiCl2Heating to 500-1000 ℃, reacting with water vapor to obtain NiO and a mixture of hydrogen chloride and water vapor, wherein the addition amount of the water vapor is NiCl2And (2) the NiO is recovered to the leaching process in the step (1) for recycling, and the mixture of the hydrogen chloride and the water vapor is condensed to obtain a hydrochloric acid product.

Claims (5)

1. The preparation method of the soda ash is characterized in that the chemical reaction formula is as follows:
Ni ( NH 3 ) 6 Cl 2 = Δ NiCl 2 + 6 NH 3 ↑
Figure A2006101353360002C2
2. the process for preparing soda ash as claimed in claim 1, wherein the process comprises the steps of:
1) dissolving NiO in CO2Adding ammonia into the mixed solution of the sodium chloride and ammonia water, absorbing ammonia until the mixed solution is saturated, adding NaCl for double decomposition, filtering and separating Na2CO3Aqueous ammonia solution and Ni (NH)3)6Cl2
2) Mixing Na2CO3Distilling ammonia water solution to remove ammonia, filtering out precipitate Ni2(OH)2CO3Concentrating and crystallizing the filtrate to obtain a soda ash product;
NiO and CO in a mass ratio2∶NaCl=100∶62∶162。
3. The process for producing soda ash as claimed in claim 2, wherein Ni (NH) is added3)6Cl2Heating to 150-200 ℃ and deaminizing to obtain NiCl2
4. The process for preparing soda ash as claimed in claim 2, wherein NiCl is added2Heating to 500-1000 ℃, reacting with water vapor to obtain NiO and a mixture of hydrogen chloride and water vapor, or reacting with O in the air2Reacting to obtain NiO and Cl2Mixing with air, recovering NiO to the leaching step in step 1 for recycling, and condensing the mixture of hydrogen chloride and water vapor to obtain hydrochloric acid product, Cl2The mixed gas with air is separated into liquid chlorine product by freezing.
5. The process for preparing soda ash as claimed in claim 4, wherein NiCl is added in a mass ratio2100: 200 of water vapor.
CNB2006101353364A 2006-12-15 2006-12-15 Sodium carbonate preparing process Expired - Fee Related CN100436322C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CNB2006101353364A CN100436322C (en) 2006-12-15 2006-12-15 Sodium carbonate preparing process

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CNB2006101353364A CN100436322C (en) 2006-12-15 2006-12-15 Sodium carbonate preparing process

Publications (2)

Publication Number Publication Date
CN1974388A true CN1974388A (en) 2007-06-06
CN100436322C CN100436322C (en) 2008-11-26

Family

ID=38124784

Family Applications (1)

Application Number Title Priority Date Filing Date
CNB2006101353364A Expired - Fee Related CN100436322C (en) 2006-12-15 2006-12-15 Sodium carbonate preparing process

Country Status (1)

Country Link
CN (1) CN100436322C (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101112998B (en) * 2007-07-09 2010-05-19 钟劲光 Preparation method of soda
CN107934964A (en) * 2017-12-18 2018-04-20 青海盐湖工业股份有限公司 A kind of carbon dioxide method of comprehensive utilization

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1113885A (en) * 1994-06-01 1995-12-27 门伟 Producing method for caustic soda
CN1151966C (en) * 2000-10-30 2004-06-02 李忠 Green chemical process for sodium carbonate production
CN1814548A (en) * 2005-12-26 2006-08-09 徐贵义 Non-waste-emission ammonia-sode process anhydrous sodium carbonate process

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101112998B (en) * 2007-07-09 2010-05-19 钟劲光 Preparation method of soda
CN107934964A (en) * 2017-12-18 2018-04-20 青海盐湖工业股份有限公司 A kind of carbon dioxide method of comprehensive utilization

Also Published As

Publication number Publication date
CN100436322C (en) 2008-11-26

Similar Documents

Publication Publication Date Title
CN108046295B (en) Method for producing sodium bicarbonate and ammonium sulfate by using sodium sulfate solution
CN113493214B (en) Novel method for preparing sodium bicarbonate and co-producing ammonium sulfate from sodium sulfate
CN111039305B (en) Method for preparing sodium bicarbonate and ammonium sulfate by sodium sulfate in short process
CN100515947C (en) Process for producing sodium carbonate using industrial salt dreg
CN112723391B (en) Process for co-producing soda ash and calcium sulfate from ammonium bicarbonate and glauberite tailings
CN114436297B (en) Method for preparing sodium carbonate from mirabilite
BG63775B1 (en) Method for potassium sulphate production
KR20150010704A (en) Selective extraction of potassium chloride from schoenite end liquor employing tartaric acid as safe, benign and recyclable extractant
CN1944291B (en) Method for teating heavy alkali filter liquid in synthesizing alkali producing method
CN114180601A (en) Green low-carbon process for producing sodium carbonate and caustic soda from waste salt and waste residues
CN1948236A (en) Method of producing potassium ammonium sulfate compound fertilizer using potassium containing rock
CA2552104C (en) Process for recovery of sulphate of potash
CN1974388A (en) Sodium carbonate preparing process
AU6170594A (en) Process for recovering solid sodium bicarbonate from diaphragm cell
CN111039304B (en) Method for preparing ammonium sulfate and sodium bicarbonate by using sodium sulfate
CN105329920A (en) Method for joint production of potassium sulphate and calcium chloride dihydrate
CN1055901C (en) Combiend production process of potassium carbonate and light magnesium carbonate
CN102085483A (en) Novel catalyst for urea method hydrazine hydrate production process
CN1796280A (en) Separation of salt and alkali from waste salt and alkali residue in production of hydrazine hydrate and technique of cyclic utilization
CN1151966C (en) Green chemical process for sodium carbonate production
WO2019082207A1 (en) Energy efficient synthesis of sulphate of potash using ammonia as a catalyst
CN1974386A (en) Sodium hydroxide preparing process
CN101786643B (en) Method for comprehensively utilizing byproduct salt and alkali waste in production of hydrazine hydrate by urea process
CN1128105C (en) Sodium carbonate extracting process from caustic lime containing sodium sulfate
CN115784263B (en) Method for preparing sodium carbonate by sodium sulfate and application thereof

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
ASS Succession or assignment of patent right

Owner name: XIAMEN YIGONG CHEMICAL SCIENCE AND TECHNOLOGY CO.,

Free format text: FORMER OWNER: ZHONG JINGUANG

Effective date: 20091211

C41 Transfer of patent application or patent right or utility model
TR01 Transfer of patent right

Effective date of registration: 20091211

Address after: Unit 289, 401422423 Weng Weng Road, Haicang District, Fujian, Xiamen

Patentee after: XIAMEN YIGONG CHEMICAL TECHNOLOGY Co.,Ltd.

Address before: Room 836, No. 704, Dong Qian Dong Road, Fujian, Xiamen

Patentee before: Zhong Jinguang

C56 Change in the name or address of the patentee

Owner name: ZHONGKE YIGONG (XIAMEN) CHEMICAL TECHNOLOGY CO., L

Free format text: FORMER NAME: XIAMEN YIGONG CHEMICAL TECHNOLOGY CO., LTD.

CP03 Change of name, title or address

Address after: Haicang District of Xiamen City, Fujian province 361026 Weng Kok Road No. 289 Chong Building 422 unit

Patentee after: ZHONGKE YIGONG (XIAMEN) CHEMICAL TECHNOLOGY Co.,Ltd.

Address before: 361022, unit 289, 401422423 Weng Weng Road, Haicang District, Fujian, Xiamen

Patentee before: XIAMEN YIGONG CHEMICAL TECHNOLOGY Co.,Ltd.

C56 Change in the name or address of the patentee

Owner name: ZHONGKE YIGONG (SHANGHAI) CHEMICAL TECHNOLOGY CO.,

Free format text: FORMER NAME: ZHONGKE YIGONG (XIAMEN) CHEMICAL TECHNOLOGY CO., LTD.

CP03 Change of name, title or address

Address after: 200030 room 6, building 829, No. 558, Xuhui District, Shanghai, Yishan Road

Patentee after: ZHONGKE YIGONG (SHANGHAI) CHEMICAL TECHNOLOGY CO.,LTD.

Address before: Haicang District of Xiamen City, Fujian province 361026 Weng Kok Road No. 289 Chong Building 422 unit

Patentee before: Zhongke Yigong (Xiamen) Chemical Technology Co.,Ltd.

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: 20081126

Termination date: 20211215