CN1143611A - Method for producing iron oxide yellow using sulfuric acid roasting residue - Google Patents

Method for producing iron oxide yellow using sulfuric acid roasting residue Download PDF

Info

Publication number
CN1143611A
CN1143611A CN 95108773 CN95108773A CN1143611A CN 1143611 A CN1143611 A CN 1143611A CN 95108773 CN95108773 CN 95108773 CN 95108773 A CN95108773 A CN 95108773A CN 1143611 A CN1143611 A CN 1143611A
Authority
CN
China
Prior art keywords
sulfuric acid
solution
oxide yellow
iron oxide
iron
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
Application number
CN 95108773
Other languages
Chinese (zh)
Inventor
廖维炎
朱新宏
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.)
Yunxi Phosphate Fertilizer Factory
Original Assignee
Yunxi Phosphate Fertilizer Factory
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 Yunxi Phosphate Fertilizer Factory filed Critical Yunxi Phosphate Fertilizer Factory
Priority to CN 95108773 priority Critical patent/CN1143611A/en
Publication of CN1143611A publication Critical patent/CN1143611A/en
Pending legal-status Critical Current

Links

Landscapes

  • Compounds Of Iron (AREA)

Abstract

A process for producing ferrite yellow as pigment with waste dregs of sulfuric acid production includes producing ferrous sulfacte from said waste dregs and transforming the ferrous sulfate into ferrite yellow, and features low cost, high quality of product and reducing environmental pollution caused by the waste dregs.

Description

The method of producing iron oxide yellow using sulfuric acid roasting residue
The present invention relates to a kind of the utilization and produce the production method that the vitriolic waste residue is a fired slags manufacturing ferric oxide yellow pigment.
The method of traditional mode of production ferric oxide yellow pigment is to produce ferrous sulfate with iron filings and sulfuric acid reaction to make through oxidation again, and the waste residue in the production sulfuric acid process is thrown away as waste product always, cause environmental pollution, and the iron that contains about 30% in this fired slags slatterns thereupon also.
The objective of the invention is to invent a kind of method of utilizing sulfuric acid roasting residue to make ferric oxide yellow pigment.
This method is made up of the following step:
A: sulfuric acid roasting residue and 21~30% dilute sulphuric acids are inserted in the acid tolerance response cylinder react, produce ferrous sulfate, the quality proportioning is between the two:
Iron: sulfuric acid=56: 98
B: in above-mentioned solution, add an amount of iron filings and make whole ferric irons be reduced to ferrous iron;
C: B is gone on foot gained solution contract evaporation concentration to original volume 2/3, naturally cooling 24 hours then has a large amount of ferrous sulfate crystal to separate out.
D: the solution that ferrous sulfate is dissolved solid carbon dioxide preparation 40%, place the acid tolerance response bucket, 30% the solution that slowly adds while stirring that the sodium hydroxide that accounts for ferrous sulfate weight 7.2~9.5% is made into, disclose the bottom from reaction simultaneously and blast filtered air with gas blower, through 20~30 hours, get the outstanding dark liquid of iron oxide yellow crystal seed.
E: above-mentioned iron oxide yellow crystal seed is added in the acid tolerance response cylinder, heat to 75~85 ℃ with steam, atmospheric oxidation behind the feeding filtration, purification slowly drips 30% sodium hydroxide solution simultaneously, exists until no ferrous ion.
F: above-mentioned solution is precipitated, and rinsing is dried to PH=7, the levigate finished product that gets.
Advantage of the present invention is the pollution problem that has solved sulfuric acid roasting residue, and production cost is low, saves a large amount of scrap iron.
Embodiment: accurately measure the iron-holder in the fired slags earlier, undertaken by following step then;
A: in iron: sulfuric acid=56: 98 ratio is inserted fired slags and dilute sulphuric acid (21~30%) in the reaction cylinder and is reacted.
B: in above-mentioned solution, add an amount of iron filings and make whole ferric iron reduction (available potassium sulfocyanate test).
C: evaporation concentration solution cooled off 24 hours to original volume 2/3.
D: ferrous sulfate is dissolved in water prepares 40% solution, place the acid tolerance response bucket, 30% the solution that slowly adds while stirring that the sodium hydroxide that accounts for ferrous sulfate weight 7.2~9.5% is made into, blast filtered air from the reaction container bottom with gas blower simultaneously, through 20~30 hours, get iron oxide yellow crystal seed suspension.
E: above-mentioned iron oxide yellow crystal seed is added in the acid tolerance response cylinder, heat to 75~85 ℃ with steam, atmospheric oxidation behind the feeding filtration, purification slowly drips 30% sodium hydroxide solution simultaneously, exists until no ferrous ion.
F: above-mentioned solution is precipitated, and rinsing is to PH=7, oven dry, levigate finished product.

Claims (1)

1, a kind of method of producing iron oxide yellow using sulfuric acid roasting residue is characterized in that being made up of the following step:
A: sulfuric acid roasting residue and 21~30% dilute sulphuric acids are inserted in the acid tolerance response cylinder react, produce ferrous sulfate, the quality proportioning is between the two:
Iron: sulfuric acid=56: 98
B: in above-mentioned solution, add an amount of iron filings and make whole ferric irons be reduced to ferrous iron;
C: B is gone on foot gained solution contract evaporation concentration to original volume 2/3, naturally cooling 24 hours then has a large amount of ferrous sulfate crystal to separate out.
D: the solution that ferrous sulfate is dissolved in water preparation 40%, place the acid tolerance response bucket, 30% the solution that slowly adds while stirring that the sodium hydroxide that accounts for ferrous sulfate weight 7.2~9.5% is made into, disclose the bottom from reaction simultaneously and blast filtered air with gas blower, through 20~30 hours, get iron oxide yellow crystal seed suspension.
E: above-mentioned iron oxide yellow crystal seed is added in the acid tolerance response cylinder, heat to 75~85 ℃ with steam, atmospheric oxidation behind the feeding filtration, purification slowly drips 30% sodium hydroxide solution simultaneously, exists until no ferrous ion.
F: above-mentioned solution is precipitated, and rinsing is dried to PH=7, the levigate finished product that gets.
CN 95108773 1995-08-24 1995-08-24 Method for producing iron oxide yellow using sulfuric acid roasting residue Pending CN1143611A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN 95108773 CN1143611A (en) 1995-08-24 1995-08-24 Method for producing iron oxide yellow using sulfuric acid roasting residue

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN 95108773 CN1143611A (en) 1995-08-24 1995-08-24 Method for producing iron oxide yellow using sulfuric acid roasting residue

Publications (1)

Publication Number Publication Date
CN1143611A true CN1143611A (en) 1997-02-26

Family

ID=5076888

Family Applications (1)

Application Number Title Priority Date Filing Date
CN 95108773 Pending CN1143611A (en) 1995-08-24 1995-08-24 Method for producing iron oxide yellow using sulfuric acid roasting residue

Country Status (1)

Country Link
CN (1) CN1143611A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101225246B (en) * 2008-01-28 2010-11-17 升华集团德清华源颜料有限公司 Special iron oxide yellow pigment for tobacco and production method thereof
CN102502870A (en) * 2011-10-21 2012-06-20 南通宝聚颜料有限公司 Preparation process of iron oxide orange pigments
CN106219611A (en) * 2016-07-27 2016-12-14 升华集团德清华源颜料有限公司 A kind of low viscosity iron oxide yellow
CN113104901A (en) * 2021-04-13 2021-07-13 江西理工大学 Method for preparing iron oxide yellow from rare earth waste acid leaching residues

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101225246B (en) * 2008-01-28 2010-11-17 升华集团德清华源颜料有限公司 Special iron oxide yellow pigment for tobacco and production method thereof
CN102502870A (en) * 2011-10-21 2012-06-20 南通宝聚颜料有限公司 Preparation process of iron oxide orange pigments
CN102502870B (en) * 2011-10-21 2013-12-11 南通宝聚颜料有限公司 Preparation process of iron oxide orange pigments
CN106219611A (en) * 2016-07-27 2016-12-14 升华集团德清华源颜料有限公司 A kind of low viscosity iron oxide yellow
CN106219611B (en) * 2016-07-27 2017-07-11 升华集团德清华源颜料有限公司 A kind of low viscosity iron oxide yellow
CN113104901A (en) * 2021-04-13 2021-07-13 江西理工大学 Method for preparing iron oxide yellow from rare earth waste acid leaching residues
CN113104901B (en) * 2021-04-13 2024-02-09 江西理工大学 Method for preparing iron oxide yellow from rare earth waste acid leaching slag

Similar Documents

Publication Publication Date Title
CN101108745A (en) Method for manufacturing iron oxide with waste slag containing iron
CN108110357A (en) A kind of method that valuable metal is recycled from positive material of waste lithium iron phosphate
CN100396733C (en) Method for producing the red pigment of ferric oxide from ferrous sulphate of byproduct abolished by titanium white
CN102021345A (en) Method for recycling vanadium pentoxide and sodium dichromate
CN108584901B (en) Method for recovering ceramic-grade iron phosphate from polymetallic hazardous wastes
CN101585554A (en) Method for preparing manganous carbonate by using waste slag and waste water containing manganese as raw materials
CN100396734C (en) Method for producing the yellow pigment of ferric oxide from ferrous sulphate of byproduct abolished by titanium white
CN113968578B (en) Method for synthesizing ferric phosphate by using titanium dioxide byproduct ferrous sulfate
CN1386710A (en) Process for preparing superfine iron oxide
CN1143611A (en) Method for producing iron oxide yellow using sulfuric acid roasting residue
CN1233562C (en) Method for preparing ferrous sulphate
CN1067269A (en) With delafossite wet method direct production copper sulfate process
CN1058201A (en) The novel process of wet producing manganese sulfate from two kinds of mine
CN1114638A (en) Process for producing ferrous sulfate by using sulfuric acid to leach pyrite cinder
CN1843939A (en) Method for preparing hybrid oxide of manganese by manganese sulfate solution
CN114084878B (en) Preparation method for synthesizing ferric phosphate by using double iron sources
CN115448285A (en) Method for preparing lithium iron phosphate by taking recycled lithium phosphate as raw material
CN1365948A (en) Process for preparing industrial beryllium oxide by sulfuric acid method
CN100363264C (en) Method of preparing tribasic lead sulphate utilizing spent lead battery plate grid and connecting piece
CN1193937C (en) Production process of high-purity ferric oxide for ferrite
CN1094014A (en) The method that directly prepares copper sulfate by chalcopyrite
CN206562305U (en) A kind of utilization containing chromium slag prepares the production system of chromium hydroxide
CN1772628A (en) Prepn process of iron red with salfated roasted dreg of sulfur containing aurin ore
CN1050367A (en) A kind of method of producing single nickel salt
CN113816354B (en) Method for preparing ferric phosphate by utilizing waste in titanium dioxide production process

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C01 Deemed withdrawal of patent application (patent law 1993)
WD01 Invention patent application deemed withdrawn after publication