CN1117947A - Method for preparation of pure cupric sulfate by using copper-contained waste liquid from preparation of guaiacol and treatment method for its waste liquid - Google Patents
Method for preparation of pure cupric sulfate by using copper-contained waste liquid from preparation of guaiacol and treatment method for its waste liquid Download PDFInfo
- Publication number
- CN1117947A CN1117947A CN 95106987 CN95106987A CN1117947A CN 1117947 A CN1117947 A CN 1117947A CN 95106987 CN95106987 CN 95106987 CN 95106987 A CN95106987 A CN 95106987A CN 1117947 A CN1117947 A CN 1117947A
- Authority
- CN
- China
- Prior art keywords
- copper sulfate
- sulfate
- waste liquid
- copper
- solution
- 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
Links
Images
Landscapes
- Removal Of Specific Substances (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
The present invention relates to a method for producing cupric sulfate by using liquid waste containing copper resulted from preparation of guaiacol and thereof treating said liquid waste. The liquid waste is cooled, then the crude cupric sulfate is settled out, which is dissolved with water and filtered off its insoluble substance, so that the cupric oxide is made up, and then the sulphuric acid is added to the cupric oxide to make a pure cupric sulfate solution which is recrystalized to obtain the pure cupric sulfate. Its residual liquid is cooled, and can be used for preparing sodium sulfate, and the pure cupric sulfate obtained by using said process can be reused in the production of guaiacol.
Description
The invention relates to a treatment technology of copper-containing waste liquid generated in the production of synthetic vanillin.
In the production of vanillin, diazonium salt is hydrolyzed to prepare the intermediate product guaiacol, and the aqueous solution of diazonium salt is hydrolyzed at a higher temperature by taking copper sulfate as a catalyst to generate the guaiacol. After the reaction is finished, high-temperature mixed waste liquid containing copper sulfate, sulfuric acid, sodium sulfate and organic matters is generated. Along with the decrease of the liquid temperature, the dissolution amount of the copper sulfate and the sodium sulfate in the solution reaches saturation, and the massive crude copper sulfate is separated out, namely the crude copper sulfate and the sulfuric acid waste liquid containing the copper sulfate can be separated. The reaction equation for the preparation of guaiacol is as follows:
(1) diazotization of anthranilic ether at low temperatureDiazonium salts
(2) Hydrolysis of diazonium salts to guaiacol in a copper sulfate mediumDistilling the hydrolysate to obtain the final product. Leaving a waste solution containing copper sulfate, sulfuric acid, sodium sulfate and organic matter. The copper is recovered from the copper-containing waste liquid by replacing copper with iron. The "production of copper sulfate by using waste copper catalyst" in 1993 volume 13, page 117 introduces a method for preparing copper sulfate from camphor-synthesizing leftover material by using combustion and extraction method. Refining copper sulfate with waste liquid of guaiacol; and the product is reused in production, and has not been reported.
The invention aims to provide a method for preparing pure copper sulfate, sodium sulfate and sulfuric acid by using copper-containing waste liquid for preparing guaiacol, and the invention also aims to provide a method for treating the waste liquid for preparing the guaiacol.
The method for preparing pure copper sulfate from the waste liquid for preparing the guaiacol comprises the following steps:
(1) cooling or evaporating and cooling the waste liquid to precipitate crude copper sulfate;
(2) the crude copper sulfate is prepared into a pure copper sulfate solution by the following method:
a. the crude copper sulfate is dissolved by adding water,
b. filtering the obtained water solution, filtering to remove insoluble substances,
c. adding sodium hydroxide into the obtained solution and heating to generate copper oxide precipitate,
d. filtering, separating out the copper oxide,
e. adding sulfuric acid into copper oxide and heating to obtain pure copper sulfate solution,
(3) and cooling the copper sulfate solution, and recrystallizing the copper sulfate to obtain the pure copper sulfate.
The method for preparing the pure copper sulfate adopts the step of preparing the copper oxide, and the pure copper sulfate can meet the standard requirement of the first-grade product of the national standard GB437-80 by filtering twice, wherein insoluble substances are removed once and dissolved substances are removed once. Can be reused in the production of vanillin.
FIG. 1 is a flow chart of the above process for preparing pure copper sulfate;
FIG. 2 is a process flow diagram of the waste acid solution;
FIG. 3 is a flow chart of the process for preparing anhydrous sodium sulfate.
As shown in fig. 1, waste heat copper sulfate solution is cooled to precipitate crude copper sulfate containing impurities, water is added to dissolve the crude copper sulfate, insoluble substances are filtered out, sodium hydroxide is added into the obtained solution, steam is introduced for heating to generate copper oxide precipitate, then the copper oxide precipitate is subjected to pressure filtration to separate out copper oxide solid, sulfuric acid is added and steam is introduced for heating to enable the copper oxide to fully react to form pure copper sulfate solution, the solution is cooled to crystallize and separate out pure copper sulfate, and then a refined copper sulfate finished product can be obtained by a centrifugal separation method. The mother liquor obtained by centrifugal separation is pure sulfuric acid and copper sulfate solution, and can be used for preparing sulfuric acid for dissolving copper oxide with concentrated sulfuric acid. The chemical reaction equation of the whole preparation process is as follows:
after the waste copper sulfate solution is cooled and precipitated to obtain crude copper sulfate, the remaining copper-containing waste sulfuric acid solution can be treated according to the method of the flow chart shown in figure 2: the copper-containing waste sulfuric acid solution is heated, evaporated and concentrated, then cooled, and crude copper sulfate is precipitated, and the copper sulfate can be refined by the above-mentioned process. The acid solution obtained by separation is sulfuric acid solution which can be used in the working procedure of dissolving copper oxide into copper sulfate.
As shown in FIG. 3, the main component of the solution left in the copper oxide filter pressing process is sodium sulfate, and the solution is cooled, i.e. precipitated and precipitated with water sodium sulfate. Separating out the sodium sulfate + water, heating and dehydrating to obtain the anhydrous sodium sulfate product.
The refining method of copper sulfate and the treatment method of waste acid liquid can recycle more than 90 percent of copper sulfate, can obtain sulfuric acid and anhydrous sodium sulfate by-products, and reduce environmental pollution.
Several examples are presented below: example 1
Refining crude copper sulfate precipitated from waste heat copper sulfate solution by cooling:
250 kg of crude copper sulfate is weighed, 500 kg of water is added, the mixture is intermittently stirred and dissolved for about 2 hours, and insoluble impurities are filtered after the solution is saturated. Adding sodium hydroxide into the filtrate while stirring until the pH is 6, introducing steam, and directly heating at 80-90 deg.C with Cu (OH)2Dehydration produces a black CuO precipitate. About 58 kg of CuO was obtained by pressure filtration. Diluting the recovered sulfuric acid with copper sulfate mother liquor at a ratio of 1: 1, and adding CuO when the temperature of the acid liquor rises to 90-95 ℃. Adding a little amount of materials within 30-40 min, and after the reaction is finished, the Baume degree of the solution is 38-42 Be', H2SO4The content is 3-49%, the mixture is sent into a crystallization kettle for crystallization, and the pure copper sulfate is obtained after the temperature is reduced to 30-35 ℃ and the material is discharged.
Example 2
Preparing sulfuric acid from copper-containing waste sulfuric acid solution:
1000 kg of copper-containing waste sulfuric acid solution with the specific gravity of 1.36 is taken out, concentrated to the specific gravity of 1.56 by using a film evaporator, discharged andnaturally cooled, and 135 kg of a mixture of solid copper sulfate and sodium sulfate is obtained, wherein the acid content of the solution is 62-68 percent. The solid is used for refining copper sulfate, the sulfuric acid solution is used for preparing copper sulfate from copper oxide, and the redundant part can be sold.
Example 3
Preparation of sodium sulfate:
and (3) taking the sodium sulfate-containing waste liquid obtained by CuO filter pressing in the embodiment 1, and placing the waste liquid in a cooler for cooling to obtain sodium sulfate decahydrate. Heating sodium sulfate decahydrate for dehydration, drying and crushing to obtain anhydrous sodium sulfate. The recovery rate can reach 60 percent.
Claims (4)
1. A method for preparing pure copper sulfate from waste liquid of guaiacol preparation comprises the following steps:
(1) cooling the waste liquid, precipitating to obtain crude copper sulfate,
(2) the crude copper sulfate is prepared into a pure copper sulfate solution,
(3) the copper sulfate solution is cooled and the copper sulfate is crystallized again to obtain pure copper sulfate,
the method for preparing the pure copper sulfate solution from the crude copper sulfate is characterized by comprising the following steps:
a. the crude copper sulfate is dissolved by adding water,
b. filtering the obtained water solution, filtering to remove insoluble substances,
c. adding sodium hydroxide into the obtained solution and heating to generate copper oxide precipitate,
d. filtering, separating out the copper oxide,
e. adding sulfuric acid into the copper oxide and heating to obtain pure copper sulfate solution.
2. The method for producing pure copper sulfate from the copper-containing waste liquid from the production of guaiacol as claimed in claim 1, wherein the sulfuric acid added in said step e is a mixture of the acid solution obtained by separating copper sulfate in said step (3) and sulfuric acid.
3. The method for producing pure copper sulfate from waste liquid from guaiacol production as claimed in claim 1 or 2, wherein said copper-containing spent acid solution obtained in step (1) is treated by: heating the waste acid solution, evaporating and concentrating, cooling and precipitating to obtain crude copper sulfate, and separating the acid solution for reuse in the step of preparing copper sulfate from copper oxide.
4. The method for preparing pure copper sulfate from the waste liquid from the preparation of guaiacol as claimed in claim 1 or 2, wherein the treatment method of the waste liquid containing sodium sulfate obtained in step d comprises: and cooling the sodium sulfate-containing waste liquid, precipitating sodium sulfate decahydrate, and heating and dehydrating the sodium sulfate decahydrate to obtain the refined anhydrous sodium sulfate.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN 95106987 CN1037763C (en) | 1995-07-13 | 1995-07-13 | Method for preparation of pure cupric sulfate by using copper-contained waste liquid from preparation of guaiacol and treatment method for its waste liquid |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN 95106987 CN1037763C (en) | 1995-07-13 | 1995-07-13 | Method for preparation of pure cupric sulfate by using copper-contained waste liquid from preparation of guaiacol and treatment method for its waste liquid |
Publications (2)
Publication Number | Publication Date |
---|---|
CN1117947A true CN1117947A (en) | 1996-03-06 |
CN1037763C CN1037763C (en) | 1998-03-18 |
Family
ID=5076169
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN 95106987 Expired - Fee Related CN1037763C (en) | 1995-07-13 | 1995-07-13 | Method for preparation of pure cupric sulfate by using copper-contained waste liquid from preparation of guaiacol and treatment method for its waste liquid |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN1037763C (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101549882B (en) * | 2008-04-03 | 2011-10-05 | 上海美维科技有限公司 | Method for preparing high-purity cupric oxide powder from acid cupriferous waste liquid |
-
1995
- 1995-07-13 CN CN 95106987 patent/CN1037763C/en not_active Expired - Fee Related
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101549882B (en) * | 2008-04-03 | 2011-10-05 | 上海美维科技有限公司 | Method for preparing high-purity cupric oxide powder from acid cupriferous waste liquid |
Also Published As
Publication number | Publication date |
---|---|
CN1037763C (en) | 1998-03-18 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
WO2018041272A1 (en) | Method for preparing industrial grade lithium carbonate from crude lithium fluoride, and a lithium carbonate product | |
CN106565956A (en) | Method for comprehensive recycling of by-product slurry in polyphenylene sulfide productive process | |
CN115947486B (en) | Desulfurization waste liquid recycling treatment process and system | |
CN112513007B (en) | DMF (dimethyl formamide) recovery method | |
CN114933288B (en) | High-purity potassium dihydrogen phosphate and preparation method thereof | |
CN114988435A (en) | Harmless treatment method for saline water in polyphenylene sulfide resin production | |
CN108585335B (en) | Method for treating phenylhydrazine hydrochloride production waste liquid and recovering resources | |
CN113214046B (en) | Method for recycling D-calcium pantothenate mother liquor | |
KR101562263B1 (en) | Method for preparing sodium nitrate using a waste solution containing nitric acid | |
CN1037763C (en) | Method for preparation of pure cupric sulfate by using copper-contained waste liquid from preparation of guaiacol and treatment method for its waste liquid | |
CN102911018B (en) | Method for separating phenol-containing organic substances from m-phenylenediamine acidic hydrolysate | |
CN101508678B (en) | Process for preparing 2-methyl-4-amino-5-acetyl aminomethyl pyrimidine | |
CN1209290C (en) | Method of preparing anhydrous aluminium chloride | |
US4908462A (en) | Cobalt recovery method | |
CN1176929C (en) | Prepn of high-purity acephate powder (1) | |
CN1156431C (en) | Process for purifying hihg-content o-methylbenzoic acid | |
CN1102141C (en) | Process for purifying 3.5-dimethyl benzoic acid | |
CN1158320A (en) | Method for reclaiming waste keto-acid liquid in prodn. of soluble gluside | |
CN112125845B (en) | Purification method of 9-phenylacridine | |
CN1203197C (en) | Method for preparing nickel and aluminium chemical product from catalyst refuse containing nickel and AL2O3 | |
CN113929561A (en) | Alkali fusion method for preparing phenolic compound | |
US4394364A (en) | Separation of boric acid from mixtures thereof with sulphuric acid | |
CN114471577B (en) | Waste Cu/ZnO/Al 2 O 3 Method for preparing new catalyst precursor by using catalyst | |
CN117586118A (en) | Recovery method of o (p) chlorobenzoic acid as byproduct of o (p) chlorobenzaldehyde | |
JPH05221632A (en) | Method for recovering salt cake from waste liquor of vanillin |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
C06 | Publication | ||
PB01 | Publication | ||
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 |