CN1047069A - Alikali cupric carbonate produced by boiling water - Google Patents
Alikali cupric carbonate produced by boiling water Download PDFInfo
- Publication number
- CN1047069A CN1047069A CN 89103226 CN89103226A CN1047069A CN 1047069 A CN1047069 A CN 1047069A CN 89103226 CN89103226 CN 89103226 CN 89103226 A CN89103226 A CN 89103226A CN 1047069 A CN1047069 A CN 1047069A
- Authority
- CN
- China
- Prior art keywords
- boiling water
- constant temperature
- crystallization
- alikali
- freeze
- 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.)
- Pending
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01G—COMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
- C01G3/00—Compounds of copper
Abstract
The present invention relates to a kind of novel process of producing ventilation breather, it uses CuSO
45H
2O and sodium bicarbonate are raw material, adopt following operation: mixed dissolution → boiling water reaction → minute filter → crystallization → freeze-day with constant temperature → check and make high purity ventilation breather cheaply is suitable for all kinds of chemical enterprises and produces in batches.
Description
The present invention relates to a kind of novel process of producing ventilation breather.
Ventilation breather is made purposes widely at medicine, chemical industry, national defence and other numerous areas, and special industrial producer that produces ventilation breather of domestic and international now none family still, just in comprehensive chemical reagent factory, with copper sulfate and soda ash is that main raw material is produced on a small quantity, people do not specialize in its manufacture craft, thereby it is very little in batches, far can not satisfy market demand, and product trash content height, the cost height.
The present invention studies the manufacture craft of ventilation breather, sums up the easy production technique of a cover, thereby realizes the purpose of production in enormous quantities, and the product purity height, and cost is low.
As Fig. 1 is technological process of production figure of the present invention.Whole process flow is like this:
Mixed dissolution → boiling water reaction → minute filter → crystallization → freeze-day with constant temperature → check.
Mixed dissolution is to be 2.29 first grade CuSO with proportion
45H
2O and the sodium bicarbonate (NaHCO that meets " Pharmacopoea Chinensis " specification
3) in scale tank (1) in the i.e. (CuSO of 1: 2 ratio
45H
2O): (NaHCO
3After porphyrize is mixed in)=1: 2, send dissolving in the dissolving tank (2); The boiling water reaction is with the mixed solution after the abundant stirring and dissolving, sends into and carries out chemical reaction (main body reaction), CO in the boiling water still (3)
2Gas is discharged from still tower upper discharge hole, and reaction conditions is that 100 ℃~200 ℃ its chemical formulas of normal pressure constant temperature are:
Dividing filter is last operation hot solution and precipitation to be sent in the separating filter (4) separates, and liquid is evaporated moisture content from the discharge of separating filter bottom, crystallization and obtain sodium sulfate, Cu
2(OH)
2CO
3Then it is sent in the crystallization kettle (5) by vacuum fan; Crystallization is with the Cu after minute filter
2(OH)
2CO
3Coarse-grain, the roasting under 100 ℃~300 ℃ constant temperature of the stoving oven in freeze-day with constant temperature chamber (6) is purified then and is obtained Cu
2(OH)
2CO
3Crystal obtains finished product with carrying out the constant temperature recrystallization again after the pure water washing; Check is the Cu with the recrystallization after drying
2(OH)
2CO
3Crystal carries out stochastic sampling and detects, and obtain Cu if produce according to above-mentioned operation
2(OH)
2CO
2>99.9%, undissolved residue<0.01%, proportion are 4 the Powdered ventilation breather of sap green monocline.
Operation that the present invention's employing is very easy and equipment are suitable for all kinds of large, medium and small chemical enterprises and adopt for the industrialized mass of ventilation breather provides an approach.
Description of drawings: Fig. 1 is technological process of production figure of the present invention.
(1) is scale tank among the figure, and (2) are dissolving tank, and (3) are reactor, and (4) are separating filter, and (5) are crystallization kettle, and (6) are the freeze-day with constant temperature chamber.
Embodiment and matters needing attention:
Producing one ton of basic carbonate copper raw material consumption according to aforementioned operation is: CuSO
45H
2The O1.5 ton, NaHCO
31.5 ton, 1000 meters in water
31000 kilowatts/time of Electric, 1 ton in coal.In the boiling water still, carry out boiling water when reaction, 200 ℃ of of boiled water temperature should be controlled at below, otherwise as equation:
Represented, ventilation breather will be decomposed into cupric oxide, and carbonic acid gas and water are in addition because Cu
2(OH)
2CO
3d
20℃=4, can check the insoluble foreign matter content of the finished product whether to be less than 0.01% so pack with constant weight.
Claims (4)
1, a kind of Alikali cupric carbonate produced by boiling water [Cu
2(OH)
2CO
3] method, it is characterized in that ventilation breather that described method is produced is is 2.29 CuSO with proportion
45H
2O and the sodium bicarbonate (NaHCO that meets " Pharmacopoea Chinensis " specification
3) make through following operation by 1: 2 proportioning as raw material: mixed dissolution → boiling water reaction → minute filter → crystallization → freeze-day with constant temperature → check.
2, method according to claim 1 is characterized in that Crystallization Procedure is the Cu that obtains after minute filter operation
2(OH)
2CO
3Coarse-grain is finished under the condition of 100 ℃~300 ℃ of constant temperature calcinings.
As method as described in the claim 1,2, it is characterized in that after Crystallization Procedure that 3, its product is again with sending the freeze-day with constant temperature operation dry and obtain the finished product after the pure water washing.
4, method according to claim 1 is characterized in that in the boiling water reaction process boiled water temperature is below 200 ℃, is preferably 100 ℃ and be reflected under the normal pressure and carry out.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN 89103226 CN1047069A (en) | 1989-05-12 | 1989-05-12 | Alikali cupric carbonate produced by boiling water |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN 89103226 CN1047069A (en) | 1989-05-12 | 1989-05-12 | Alikali cupric carbonate produced by boiling water |
Publications (1)
Publication Number | Publication Date |
---|---|
CN1047069A true CN1047069A (en) | 1990-11-21 |
Family
ID=4855035
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN 89103226 Pending CN1047069A (en) | 1989-05-12 | 1989-05-12 | Alikali cupric carbonate produced by boiling water |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN1047069A (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7713567B2 (en) | 2001-02-13 | 2010-05-11 | The Folgers Coffee Company | Method of making coffee compositions with stable flavor characteristics |
US7713568B2 (en) | 2001-02-15 | 2010-05-11 | The J.M. Smucker Company | Method of making coffee compositions with stable flavor characteristics |
CN101195497B (en) * | 2006-12-04 | 2012-10-03 | 沈祖达 | Process for producing cupric hydroxide or cupric oxide |
CN103864133A (en) * | 2012-12-11 | 2014-06-18 | 财团法人工业技术研究院 | Preparation method of nano metal salt and formation method of absorption layer of solar cell |
CN105502472A (en) * | 2014-10-15 | 2016-04-20 | 刘浩 | Preparation method of basic copper carbonate |
CN106976902A (en) * | 2016-11-30 | 2017-07-25 | 佛山市兴华源机械设备有限公司 | A kind of method for preparing basic copper carbonate using industrial copper-containing etching waste solution |
-
1989
- 1989-05-12 CN CN 89103226 patent/CN1047069A/en active Pending
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7713567B2 (en) | 2001-02-13 | 2010-05-11 | The Folgers Coffee Company | Method of making coffee compositions with stable flavor characteristics |
US7713568B2 (en) | 2001-02-15 | 2010-05-11 | The J.M. Smucker Company | Method of making coffee compositions with stable flavor characteristics |
CN101195497B (en) * | 2006-12-04 | 2012-10-03 | 沈祖达 | Process for producing cupric hydroxide or cupric oxide |
CN103864133A (en) * | 2012-12-11 | 2014-06-18 | 财团法人工业技术研究院 | Preparation method of nano metal salt and formation method of absorption layer of solar cell |
CN105502472A (en) * | 2014-10-15 | 2016-04-20 | 刘浩 | Preparation method of basic copper carbonate |
CN106976902A (en) * | 2016-11-30 | 2017-07-25 | 佛山市兴华源机械设备有限公司 | A kind of method for preparing basic copper carbonate using industrial copper-containing etching waste solution |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN109761209A (en) | A kind of production technology and its production equipment of ferric phosphate | |
CN113428882A (en) | Method for preparing battery-grade lithium carbonate from spodumene | |
CN108584962B (en) | Acid steam prepurification metallic silicon process and surface purification equipment | |
CN1297847A (en) | Comprehensive utilization method of waste ammonia sode liquid and sodium sulfate containing waste liquid | |
CN1047069A (en) | Alikali cupric carbonate produced by boiling water | |
CN113042059A (en) | Preparation method of red mud-based catalyst for biomass pyrolysis | |
CN101367542A (en) | Preparation method for high purity silver nitrate | |
CN1053081A (en) | A kind of method of synthesizing paraffin chloride | |
CN101891256A (en) | Production technique of high-purity potassium permanganate and manganese dioxide, and carbon dioxide reaction tower | |
CN106435186B (en) | Cobalt scrap acid hydrolyzation and preparing the application in cobaltosic oxide high-purity cobalt liquid | |
CN109850911B (en) | System and method for preparing ultrafine silicon dioxide by leaching silicate ore by using hydrogen chloride gas | |
CN209974312U (en) | System for utilize hydrogen chloride gas leaching silicate ore preparation superfine silicon dioxide | |
CN1043044C (en) | Method for preparation of hydroxy-ethylene-diphosphonic acid | |
CN1149294C (en) | Method of extracting metal gallium frojm smelting smoke dust of corundum arc furnace | |
CN101671087B (en) | Method for recovering reagent grade sodium nitrate from waste liquid of bismuth subnitrate production | |
CN1202016C (en) | Production process of tetrahydrated zirconium sulfate | |
CN102849777A (en) | Production process of active copper oxide | |
CN103159236A (en) | Production method of environmental-protective grade magnesium hydroxide | |
CN112456545A (en) | Method for preparing sodium stannate trihydrate by using tin stripping waste liquid | |
CN1107903A (en) | Method for preparing sodium hydroxide by brine electrolysis | |
CN212864145U (en) | Phosphoric acid dearsenification system | |
CN212594083U (en) | Sodium sulfide continuous cooling crystallization system | |
CN210855283U (en) | Automation equipment of chemical purification graphite | |
CN107827149A (en) | A kind of production method of the sodium stannate of low leaded antimony arsenic iron tramp | |
CN1078444A (en) | The preparation method of alkali metal stannate |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
C06 | Publication | ||
PB01 | Publication | ||
C01 | Deemed withdrawal of patent application (patent law 1993) | ||
WD01 | Invention patent application deemed withdrawn after publication |