[go: up one dir, main page]

CN1042842C - Method for prodn. of sodium chlorate by enclosed circulation of non-evaporating mother liquor - Google Patents

Method for prodn. of sodium chlorate by enclosed circulation of non-evaporating mother liquor Download PDF

Info

Publication number
CN1042842C
CN1042842C CN93111198A CN93111198A CN1042842C CN 1042842 C CN1042842 C CN 1042842C CN 93111198 A CN93111198 A CN 93111198A CN 93111198 A CN93111198 A CN 93111198A CN 1042842 C CN1042842 C CN 1042842C
Authority
CN
China
Prior art keywords
salt
sodium chlorate
sodium
enters
mother liquor
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
CN93111198A
Other languages
Chinese (zh)
Other versions
CN1085962A (en
Inventor
谭秉彝
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 CN93111198A priority Critical patent/CN1042842C/en
Publication of CN1085962A publication Critical patent/CN1085962A/en
Application granted granted Critical
Publication of CN1042842C publication Critical patent/CN1042842C/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Landscapes

  • Electrolytic Production Of Non-Metals, Compounds, Apparatuses Therefor (AREA)

Abstract

一种电解食盐生产氯酸钠的方法,包括电解饱和食盐水溶液制备氯酸钠并将电解完成液置入氯化钠增浓器中以工业食盐将其中NaCl浓度提高到120~165g/l,加入尿素、烧碱、纯碱、氯化钡以除去次氯酸盐、镁、钙和硫酸根离子后进入冷冻结晶罐而折出结晶,经分离、干燥而得产品。母液进入溶盐罐制成饱和食盐水再次电解。这一闭路循环工艺避免六价铬离子处理和污染环境,并节省能源、降低成本、提高产品质量。设备中的增浓器设计新颖,作用大且效率高。A method for producing sodium chlorate by electrolyzing salt, comprising preparing sodium chlorate by electrolyzing a saturated salt solution and putting the electrolyzed solution into a sodium chloride thickener to increase the NaCl concentration to 120-165 g/l with industrial salt, adding Urea, caustic soda, soda ash, and barium chloride are removed from hypochlorite, magnesium, calcium, and sulfate ions, and then enter the freezing crystallization tank to fold out the crystals, separate, and dry to obtain the product. The mother liquor enters the salt-dissolving tank to make saturated salt water and electrolyzes again. This closed-loop process avoids the treatment of hexavalent chromium ions and pollutes the environment, saves energy, reduces costs, and improves product quality. The thickener in the equipment is novel in design, powerful in function and high in efficiency.

Description

The method of the production sodium chlorate that electrolyzes table salt
The present invention relates to a kind of method of the production sodium chlorate that electrolyzes table salt, particularly use subzero fractionation method production sodium chlorate.
Sodium chlorate is increasing as its consumption of SYNTHETIC OPTICAL WHITNER such as paper pulp, fabric, and Gross World Product reaches 1,430,000 tons/year.At present, the production technique of sodium chlorate is still based on the salt electrolysis method, and its flow process as shown in Figure 1.This technical process greatest drawback be solution repeatedly vacuum-evaporation concentrate, energy dissipation is big; Secondly concentrate back Cr 6+Concentration also increases, and its barium salt also needs Application and Development after the precipitation process, otherwise contaminate environment, content overproof in the sodium chlorate product simultaneously; Have again sodium chlorate liquid concentrate the back than great (850~900g/l), very easily with the sodium-chlor particle suspension in solution, then need clarify precipitation for what get rid of, evaporation once more caused waste after precipitation also need be dissolved.
The present invention its objective is on the basis with the salt electrolysis method, changes traditional method of evaporation and is separated into the subzero fractionation method, and a whole set of new separating technology is provided, thereby avoids defective such as the miscellaneous and energy dissipation of technology.
Electrolysis section of the present invention still adopts the outer circulation type electrolyzer, the electrolysis saturated common salt aqueous solution, and its flow process sees shown in the accompanying drawing 2, and electrolysis makes that density of sodium chlorate reaches about 550g/l in the electrolytic solution, and sodium-chlor reaches 100~110g/l, uses NaClO then 3-NaCl-H 2The mixed dissolution degree principle of O adopts industrial crude salt to improve sodium chloride concentration in the sodium-chlor enrichment device of special use, makes it reach 120~165g/l.And the utilization electrolysis is finished liquid self temperature (need not heat) and is added urea, caustic soda, soda ash and bariumchloride to handle impurity such as by product hypochlorite and magnesium, calcium, sulfate ion, after separating its throw out, clear liquid enters the crystallisation by cooling jar, folds NaClO under 80~160 rev/mins stirrings and-10~5 ℃ 3Crystal, crystal carries out dry packing and becomes product after separating.Entering of mother liquor salt operation enters electrolytic system after dissolving makes sodium-chlor reach 240~270g/l with salt, electrolysis once more, so repeatedly.Special-purpose sodium-chlor enrichment device as shown in Figure 3, it act as: the one, add sodium-chlor and make its concentration reach 120~165g/l, the crystallization that prevents sodium-chlor is not on the other hand dissolved and is flowed in the crystallisation by cooling jar and make that sodium chloride content exceeds standard in the crystalline sodium chlorate.Its size two drums that are configured to be made by the titanium material are formed, and outer bucket diameter is 1.7~2.2 times of interior bucket diameter, and interior bucket is than the high 200mm of outer bucket, as outer bucket diameter 600mm, high 1200mm, on the outlet pipe of band micropore is arranged, discharging hole is arranged down; An interior bucket diameter is 350mm, high 1400mm, and 4 100 * 100mm perforates are arranged symmetrically at the bottom, and electrolytic solution and industrial crude salt enter on interior bucket, constantly dissolve the back from perforate effusion down, return up from the outlet pipe of band micropore to spill out.The crystallisation by cooling jar has the chuck and the agitator that can lead to chilled brine for to make with stainless steel, and requiring mixing speed is 80~160 rev/mins, and temperature is-10~5 ℃.Because the closed cycle of mother liquor, the dichromate of adding does not run off, and not enrichment reduces consuming and three wastes processing.
Method of the present invention relatively has its outstanding feature with the method for evaporation of usefulness:
(1) technology is simple and reasonable.1. utilize the sodium-chlor temperature variation and solubleness is constant, and sodium chlorate under certain sodium chloride concentration through freezing crystallizable separating out (NaCl does not separate out simultaneously), this is just avoided repeatedly evaporation concentration to waste energy and the time, simplifies technology.2. there is not the enrichment of dichromate in mother liquor closed cycle, without special disposal, and non-hexavalent chromium ionic soil environment.3. electrolytic solution reduces cost without refined salt with Industrial Salt enrichment sodium chloride concentration.
(2) equipment reduces, and the novel and efficient height of sodium-chlor enrichment device, the crystallisation by cooling jar set up.
(3) because energy expenditure greatly reduces with cold method replacement method of evaporation.Frozen portions of the present invention is partly compared with method of evaporation, and its energy consumption has descended 97%.
(4) quality product surpasses national standard.In eight indexs, there are five to be better than the product that method of evaporation is produced.Should be mentioned that especially the product appearance of producing with method of the present invention is pure white, crystal form is the quicksand shape, and exhausted nothing has caking.
(5) product cost descends more than 12% than method of evaporation.
Fig. 1 is the production sodium chlorate prior art separation process scheme figure that electrolyzes table salt.Fig. 2 is separation process scheme figure of the present invention.Fig. 3 is a sodium-chlor enrichment device synoptic diagram, and electrolytic solution and industrial crude salt are entered by interior bucket top, and the dissolving back enters outer bucket by interior bucket lower opening place gradually, is flowed out by outer bucket top band micropore outlet pipe.
Example
Drop into electrolysis and finish liquid 4.5m 3, NaClO wherein 3Be 565g/l, NaCl102g/l; In sodium-chlor enrichment device, throw industrial crude salt 230kg (containing NaCl92.5%) then NaCl concentration rise to 148g/l, add urea 4kg, caustic soda 6.75kg, Na 2CO 34.5kg BaCl26.75kg is to remove impurity such as hypochlorite and magnesium, calcium, sulfate ion.Electrolytic solution after the processing is made a gift to someone in the freezing and crystallizing jar, under-10~5 ℃, 80 rev/mins mixing speed, separate out crystallization and separate NaClO 3820kg gets product 758kg after the drying.Mother liquor enters the molten system saturated brine of dissolved salt jar, wherein K 2Cr 2O 7Content is 2.5g/l, is used for electrolysis once more.Product all reaches country-level standard.

Claims (3)

1、一种电解食盐生产氯酸钠的方法,包括电解饱和食盐水溶液制各含550g/l的氯酸钠和100~110g/l的氯化钠电解液,其特征为电解完成液于氯化钠增浓器中加工业原盐提高其中NaCl浓度为120~165g/l,加入尿素、烧碱、纯碱、BaCl2以处理除去次氯酸盐、镁、钙及硫酸根离子,溶液进入冷冻结晶罐,在80~160转/分钟的搅拌和-10~5℃下折出晶体,经分离、干燥而得产品;母液进入化盐工序,加盐溶解使NaCl达240~270g/l后进入电解系统再次电解。1, a kind of method for producing sodium chlorate by electrolytic table salt, comprise the sodium chlorate electrolytic solution that each contains 550g/l sodium chlorate and 100~110g/l sodium chloride electrolytic solution, it is characterized in that electrolysis completes liquid in chlorination Raw salt in the processing industry is increased in the sodium concentrator, and the NaCl concentration is 120-165g/l. Add urea, caustic soda, soda ash, and BaCl to remove hypochlorite, magnesium, calcium, and sulfate ions. The solution enters the freezing crystallization tank. Stirring at 80-160 rpm and at -10-5°C, the crystals are folded out, separated and dried to obtain the product; the mother liquor enters the salt process, and the salt is dissolved to make NaCl reach 240-270g/l, and then enters the electrolysis system again electrolysis. 2、如权利要求1所述的电解食盐生产氯酸钠的方法,其特征为所述的氯化钠增浓器结构为:由大小两圆桶组成,外桶直径是内桶直径的1.7~2.2倍,外桶高1200mm,桶上方有带微孔的出口管,下部有排净口;内桶比外桶高200mm,下部均匀对称有4个100×100mm开孔,电解液与工业原盐由内桶上端进入,不断溶解后从下开孔逸出,返上至外桶上方出口管流出。2. The method for producing sodium chlorate by electrolyzing table salt as claimed in claim 1, characterized in that the structure of the sodium chloride thickener is as follows: it consists of two drums, the diameter of which is 1.7 to 2.2 diameters of the diameter of the inner drum. times, the height of the outer barrel is 1200mm, there is an outlet pipe with micro-holes on the top of the barrel, and a drain port at the bottom; the inner barrel is 200mm higher than the outer barrel, and there are four holes of 100×100mm evenly and symmetrically in the lower part, and the electrolyte and industrial raw salt come from the upper end of the inner barrel It enters, dissolves continuously, escapes from the lower opening, and returns to the outlet pipe above the outer barrel to flow out. 3、如权利要求1或2所述的电解食盐生产氯酸钠的方法,其特征为氯化钠增浓器是由钛材制成。3. The method for producing sodium chlorate by electrolyzing table salt as claimed in claim 1 or 2, characterized in that the sodium chloride thickener is made of titanium.
CN93111198A 1993-05-31 1993-05-31 Method for prodn. of sodium chlorate by enclosed circulation of non-evaporating mother liquor Expired - Fee Related CN1042842C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN93111198A CN1042842C (en) 1993-05-31 1993-05-31 Method for prodn. of sodium chlorate by enclosed circulation of non-evaporating mother liquor

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN93111198A CN1042842C (en) 1993-05-31 1993-05-31 Method for prodn. of sodium chlorate by enclosed circulation of non-evaporating mother liquor

Publications (2)

Publication Number Publication Date
CN1085962A CN1085962A (en) 1994-04-27
CN1042842C true CN1042842C (en) 1999-04-07

Family

ID=4989001

Family Applications (1)

Application Number Title Priority Date Filing Date
CN93111198A Expired - Fee Related CN1042842C (en) 1993-05-31 1993-05-31 Method for prodn. of sodium chlorate by enclosed circulation of non-evaporating mother liquor

Country Status (1)

Country Link
CN (1) CN1042842C (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103290428B (en) * 2013-06-17 2015-07-01 广西大学 Closed cycle pollution-free sodium chlorate production process
CN106757134A (en) * 2015-11-25 2017-05-31 湖南恒光化工有限公司 A kind of production technology of anti-caking sodium chlorate
CN106591876B (en) * 2016-12-20 2019-04-02 四川岷江雪盐化有限公司 A method of sodium chlorate is prepared by Nacl

Citations (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US488809A (en) * 1892-12-27 Conrad heepe
US2511516A (en) * 1945-10-31 1950-06-13 Western Electrochemical Compan Process for making sodium chlorate
US2797192A (en) * 1953-07-02 1957-06-25 Electro Chimie Metal Electrolytic preparation of alkaline chlorates
US3043757A (en) * 1959-07-08 1962-07-10 Olin Mathieson Electrolytic production of sodium chlorate
US3219563A (en) * 1960-06-22 1965-11-23 Ici Ltd Multi-electrolytic cell comprising a plurality of diaphragm-free unit cells and the use of same for preparing alkali metal chlorates
US3511619A (en) * 1965-11-30 1970-05-12 Hooker Chemical Corp Crystallization of alkali metal chlorate from an alkali metal chloratealkali metal chloride solution
US3574095A (en) * 1968-08-30 1971-04-06 Gothe O Westerlund Chlorate system
CN87102399A (en) * 1986-03-27 1987-10-07 雅士兰石油公司 Tin or bismuth coordination catalyst and relative coating cause and solidify
US4702805A (en) * 1986-03-27 1987-10-27 C-I-L Inc. Production of sodium chlorate
US4888099A (en) * 1986-02-10 1989-12-19 Eka Nobel Ab Process for the production of alkali metal chlorate
CN1052152A (en) * 1989-11-29 1991-06-12 阿托化学公司 Production of alkali metal chlorates or perchlorates
US5104500A (en) * 1990-04-30 1992-04-14 Occidental Chemical Corporation Ion exchange removal of impurities from chlorate process liquors

Patent Citations (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US488809A (en) * 1892-12-27 Conrad heepe
US2511516A (en) * 1945-10-31 1950-06-13 Western Electrochemical Compan Process for making sodium chlorate
US2797192A (en) * 1953-07-02 1957-06-25 Electro Chimie Metal Electrolytic preparation of alkaline chlorates
US3043757A (en) * 1959-07-08 1962-07-10 Olin Mathieson Electrolytic production of sodium chlorate
US3219563A (en) * 1960-06-22 1965-11-23 Ici Ltd Multi-electrolytic cell comprising a plurality of diaphragm-free unit cells and the use of same for preparing alkali metal chlorates
US3511619A (en) * 1965-11-30 1970-05-12 Hooker Chemical Corp Crystallization of alkali metal chlorate from an alkali metal chloratealkali metal chloride solution
US3574095A (en) * 1968-08-30 1971-04-06 Gothe O Westerlund Chlorate system
US4888099A (en) * 1986-02-10 1989-12-19 Eka Nobel Ab Process for the production of alkali metal chlorate
CN87102399A (en) * 1986-03-27 1987-10-07 雅士兰石油公司 Tin or bismuth coordination catalyst and relative coating cause and solidify
US4702805A (en) * 1986-03-27 1987-10-27 C-I-L Inc. Production of sodium chlorate
CN1052152A (en) * 1989-11-29 1991-06-12 阿托化学公司 Production of alkali metal chlorates or perchlorates
US5104500A (en) * 1990-04-30 1992-04-14 Occidental Chemical Corporation Ion exchange removal of impurities from chlorate process liquors

Also Published As

Publication number Publication date
CN1085962A (en) 1994-04-27

Similar Documents

Publication Publication Date Title
US3655331A (en) Production of sodium carbonate
CN110157913A (en) A kind of method of copper ashes integrated treatment
CN106865859A (en) A kind of method of integrated treatment chemical industry strong brine
NO145376B (en) PROCEDURE FOR CONCENTRATION AND CLEANING MGCL2 LUT
CN100471794C (en) Production of Potassium Chloride by Adding Brine
CN1042842C (en) Method for prodn. of sodium chlorate by enclosed circulation of non-evaporating mother liquor
US3212848A (en) Process for producing sodium carbonate
CN100515946C (en) Process for producing potassium chloride from potassium mixed salt produced from sulfate-type brine and old brine
CN110025973A (en) A kind of crystallizer
CN106379861B (en) The production equipment and method of a kind of potassium hyperchlorate
Lozano Recovery of potassium magnesium sulfate double salt from seawater bittern
BRPI0318666B1 (en) integrated process for the preparation of potassium sulphate
CN106495189A (en) A kind of production method of high-purity food-grade potassium chloride
CN108439436A (en) A kind of preparation process of sulfuric acid monohydrate lithium
CN1027883C (en) Pren. method of potassium sulfate from bittern and potassium chloride
CN1044108C (en) Method for preparing potassium sulfate with sulfate type bittern
CN208732632U (en) The production equipment of sodium bicarbonate
CN1179882C (en) Process for preparing potassium sulfate
CN206645962U (en) A kind of integrated treatment chemical industry strong brine system
CN100402426C (en) A method for producing refined salt by utilizing sodium-containing brine
CN103991851A (en) New process for green and cyclic production of hydrazine hydrate
AU2002232114B2 (en) A process for recovery of low sodium salt from bittern
CN205973780U (en) Production facility of potassium chlorate
CN106379860B (en) A kind of production equipment and method of potassium chlorate
CN1035096A (en) The method of high temp. salt system sal epsom and sodium-chlor

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