CN110028045A - Utilize the method for calcium metaborate concentration titanium white waste acid - Google Patents

Utilize the method for calcium metaborate concentration titanium white waste acid Download PDF

Info

Publication number
CN110028045A
CN110028045A CN201910334849.5A CN201910334849A CN110028045A CN 110028045 A CN110028045 A CN 110028045A CN 201910334849 A CN201910334849 A CN 201910334849A CN 110028045 A CN110028045 A CN 110028045A
Authority
CN
China
Prior art keywords
titanium white
waste acid
white waste
concentration
calcium metaborate
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.)
Withdrawn
Application number
CN201910334849.5A
Other languages
Chinese (zh)
Inventor
穆宏波
穆天柱
邓斌
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.)
Chengdu Advanced Metal Materials Industry Technology Research Institute Co Ltd
Original Assignee
Chengdu Advanced Metal Materials Industry Technology Research Institute Co Ltd
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 Chengdu Advanced Metal Materials Industry Technology Research Institute Co Ltd filed Critical Chengdu Advanced Metal Materials Industry Technology Research Institute Co Ltd
Priority to CN201910334849.5A priority Critical patent/CN110028045A/en
Publication of CN110028045A publication Critical patent/CN110028045A/en
Withdrawn legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B17/00Sulfur; Compounds thereof
    • C01B17/69Sulfur trioxide; Sulfuric acid
    • C01B17/88Concentration of sulfuric acid

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Heat Treatment Of Water, Waste Water Or Sewage (AREA)

Abstract

The invention discloses a kind of methods using calcium metaborate concentration titanium white waste acid, belong to chemical field, the following steps are included: titanium white waste acid and calcium metaborate are respectively placed in same closed container, the sulfuric acid for being 50~55% to get mass percentage concentration after the completion of to be concentrated.The method of the present invention completely avoids the use of boiler and evaporator, avoid the use of expensive resistant material, to reduce production cost, and operation it is at normal temperature or slightly hot under conditions of carry out, operating condition is significantly improved in this way, but also the economy of titanium white waste acid concentration is improved.

Description

Utilize the method for calcium metaborate concentration titanium white waste acid
Technical field
The invention belongs to chemical fields, and in particular to a method of titanium white waste acid is concentrated using calcium metaborate.
Background technique
Titanium White Production By Sulfuric Acid Process will generate Waste Sulfuric Acid (abbreviation titanium white waste acid) and the green vitriol containing 7 crystallizations water (FeSO4·7H2O), when using ilmenite concentrate, (main component is metatitanic acid iron FeTiO3, wherein TiO2Content be 45-50wt%) be When raw material, 1 ton of titanium dioxide is generally produced by seven inkstone of output 3.5-4 ton, while generating 7~8 tons and containing 17~20% sulfuric acid Titanium white waste acid.
Due to too big using the waste sulfuric acid solution quantum of output of method for producing gtitanium dioxide with sulphuric acid by-product, and contain a certain amount of sulphur It is sour ferrous, so that this waste sulfuric acid solution can not be utilized in other fields using dilute sulfuric acid.Lime is generallyd use at present In stone and generate calcium sulfate method titanium white waste acid is handled, however, obtained calcium sulfate there is no utility value and can only Stockpiling, this does not utilize raw material not only well, but also biggish pressure can be caused to environment.Positive method is first to lead to When crossing preliminary evaporation and concentration and improving the mass percentage concentration of sulfuric acid to 30%~40%, ferrous sulfate is isolated;Further Evaporation and concentration becomes 50% or more sulfuric acid, returns to acidolysis operation, uses for continuous acidolysis, to completely be utilized.But It is that the corrosivity of sulfuric acid solution at high temperature is extremely strong, it is desirable that be worth higher graphite material, while being concentrated by evaporation and needing large capacity Steam boiler so that the equipment investment of this method is high and production cost is also high.
Summary of the invention
The technical problem to be solved by the present invention is to it is existing concentration titanium white waste acid method it is big to equipment corrosion, it is at high cost.
The technical solution of present invention solution above-mentioned technical problem are as follows: provide a kind of utilization calcium metaborate concentration titanium white waste acid Method, comprising the following steps: titanium white waste acid and calcium metaborate are respectively placed in same closed container, after the completion of to be concentrated, The sulfuric acid for being 50~55% up to mass percentage concentration.
Wherein, the above-mentioned method using calcium metaborate concentration titanium white waste acid, the quality percentage of sulfuric acid in the titanium white waste acid Concentration is 17~20%.
Wherein, it is above-mentioned using calcium metaborate concentration titanium white waste acid method, the calcium metaborate be two water calcium metaborates or Four water calcium metaborates.
Wherein, the above-mentioned method using calcium metaborate concentration titanium white waste acid, the quality of the titanium white waste acid and calcium metaborate Than for 1:1.35~6.
Wherein, the above-mentioned method using calcium metaborate concentration titanium white waste acid, the quality of the titanium white waste acid and calcium metaborate Than for 1:1.35~3.
Wherein, the above-mentioned method using calcium metaborate concentration titanium white waste acid, the temperature of the concentration are 10~38 DEG C.
Wherein, the above-mentioned method using calcium metaborate concentration titanium white waste acid, the time of the concentration are 3~7 days.
Compared with prior art, the beneficial effects of the present invention are:
The method of the present invention completely avoids the use of boiler and evaporator, avoids the use of expensive resistant material, To reduce production cost, and operate it is at normal temperature or slightly hot under conditions of carry out, significantly improve work in this way Condition, but also the economy of titanium white waste acid concentration is improved.
The raw material calcium metaborate that the present invention uses can recycle, and greatly reduce the cost of raw material.
Specific embodiment
Specifically, a kind of method using calcium metaborate concentration titanium white waste acid, comprising the following steps: by titanium white waste acid and partially Line borate is respectively placed in same closed container, the sulfuric acid for being 50~55% to get mass percentage concentration after the completion of to be concentrated.
The mass percentage concentration of sulfuric acid is 17~20% in titanium white waste acid used in the method for the present invention.
In method of the invention, in the method for the present invention, calcium metaborate selection has hygroscopic two water calcium metaborate or four The better two water calcium metaborate of water calcium metaborate, preferably hygroscopicity.
In the method for the present invention, the dosage of calcium metaborate and the time of concentration are to be mutually related: the dosage of calcium metaborate is more, Then concentration time is short, and the dosage of calcium metaborate is few, then the time being concentrated is short.
A specific embodiment of the invention is further described below with reference to embodiment, is not therefore limited the present invention System is among the embodiment described range.
Embodiment 1
By 100 grams of this Waste Sulfuric Acids, wherein the ferrous sulfate of sulfuric acid and 2~3wt% containing 20wt%.With 135 gram of two water Calcium metaborate (CaB2O4·2H2O) be respectively placed in same closed container at normal temperature, (pay attention to two kinds of materials it is separated, It cannot mix).Two kinds of materials are taken out after 7 days, liquid is the sulfuric acid of 50~55wt%, and solid is six water calcium metaborate (CaB2O4· 6H2O), the removing crystallization water is dried at 300~350 DEG C in solid phase, becomes two water calcium metaborate (CaB2O4·2H2O) returning makes With.The sulfuric acid of 50~55wt% can return to acidolysis and use for continuous acidolysis.
Embodiment 2
By 100 grams of this Waste Sulfuric Acids, wherein the ferrous sulfate of sulfuric acid and 2~3wt% containing 20wt%.With 270 gram of two water Calcium metaborate (CaB2O4·2H2O) be respectively placed in same closed container at normal temperature, (pay attention to two kinds of materials it is separated, It cannot mix).Two kinds of materials are taken out after 3.5 days, liquid is the sulfuric acid of 50~55wt%, and solid is four water calcium metaborates (CaB2O4·4H2O), the removing crystallization water is dried at 300~350 DEG C in solid phase, becomes two water calcium metaborate (CaB2O4· 2H2O it) returns and uses.The sulfuric acid of 50~55wt% can return to acidolysis and use for continuous acidolysis.
Embodiment 3
In order to improve two water calcium metaborate (CaB2O4·2H2O utilization rate) can use the mode of operation of " adverse current ".
By the finally obtained solid phase CaB of embodiment 22O4·4H2O continues to put respectively at normal temperature with 100 grams of new Waste Sulfuric Acids It is placed in same closed container, (notice that two kinds of materials are separated, cannot mix).Two kinds of materials are taken out after 7 days, liquid is The sulfuric acid of 50wt%, solid are six water calcium metaborate (CaB2O4·6H2O), removing crystallization is dried at 300~350 DEG C Water becomes CaB2O4·2H2O, which is returned, to be used.
The sulfuric acid of 50wt% continues and CaB2O4·2H2O is respectively placed at normal temperature in same closed container, (is paid attention to Two kinds of materials are separated, cannot mix).Two kinds of materials are taken out after 3.5 days, liquid is the sulfuric acid of 55wt%, returns to acidolysis and supplies Continuous acidolysis uses;Solid phase calcium metaborate still has the space of water suction, continues to act on new Waste Sulfuric Acid, until it is saturated and becomes CaB2O4·6H2O is dried the removing crystallization water at 300~350 DEG C, becomes CaB2O4·2H2O, which is returned, to be used;Liquid phase continues With new CaB2O4·2H2O effect, until liquid concentration reaches 55wt% and stops.

Claims (7)

1. utilizing the method for calcium metaborate concentration titanium white waste acid, which comprises the following steps: by titanium white waste acid and inclined boron Sour calcium is respectively placed in same closed container, the sulfuric acid for being 50~55% to get mass percentage concentration after the completion of to be concentrated.
2. utilizing the method for calcium metaborate concentration titanium white waste acid according to claim 1, it is characterised in that: the titanium white waste acid The mass percentage concentration of middle sulfuric acid is 17~20%.
3. utilizing the method for calcium metaborate concentration titanium white waste acid according to claim 1, it is characterised in that: the calcium metaborate For two water calcium metaborates or four water calcium metaborates.
4. utilizing the method for calcium metaborate concentration titanium white waste acid according to claim 1, it is characterised in that: the titanium white waste acid Mass ratio with calcium metaborate is 1:1.35~6.
5. utilizing the method for calcium metaborate concentration titanium white waste acid according to claim 4, it is characterised in that: the titanium white waste acid Mass ratio with calcium metaborate is 1:1.35~3.
6. utilizing the method for calcium metaborate concentration titanium white waste acid according to claim 1, it is characterised in that: the temperature of the concentration Degree is 10~38 DEG C.
7. according to claim 1 using calcium metaborate concentration titanium white waste acid method, it is characterised in that: the concentration when Between be 3~7 days.
CN201910334849.5A 2019-04-24 2019-04-24 Utilize the method for calcium metaborate concentration titanium white waste acid Withdrawn CN110028045A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201910334849.5A CN110028045A (en) 2019-04-24 2019-04-24 Utilize the method for calcium metaborate concentration titanium white waste acid

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201910334849.5A CN110028045A (en) 2019-04-24 2019-04-24 Utilize the method for calcium metaborate concentration titanium white waste acid

Publications (1)

Publication Number Publication Date
CN110028045A true CN110028045A (en) 2019-07-19

Family

ID=67240132

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201910334849.5A Withdrawn CN110028045A (en) 2019-04-24 2019-04-24 Utilize the method for calcium metaborate concentration titanium white waste acid

Country Status (1)

Country Link
CN (1) CN110028045A (en)

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101525187A (en) * 2009-03-24 2009-09-09 四川大学 Method for concentrating titanium pigment waste acid
CN101538023A (en) * 2008-03-22 2009-09-23 四川大学 Processing method for titanium pigment waste acid
CN102910594A (en) * 2012-11-06 2013-02-06 黄正源 Method for concentrating waste sulfuric acid by utilizing waste heat of titanium dioxide calcinator

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101538023A (en) * 2008-03-22 2009-09-23 四川大学 Processing method for titanium pigment waste acid
CN101525187A (en) * 2009-03-24 2009-09-09 四川大学 Method for concentrating titanium pigment waste acid
CN102910594A (en) * 2012-11-06 2013-02-06 黄正源 Method for concentrating waste sulfuric acid by utilizing waste heat of titanium dioxide calcinator

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
朱洪法 等: "《无机化工产品手册》", 31 December 2008, 金盾出版社 *

Similar Documents

Publication Publication Date Title
CN102249471A (en) Method for processing battery-level lithium carbonate mother liquor
CN107857243A (en) The method that titanium white by product thing ferrous sulfate prepares LITHIUM BATTERY superfine iron phosphate
US20220135425A1 (en) Method for Co-Producing Synthetical Rutile and Polymeric Ferric Sulfate with Waste Sulfuric Acid
WO2021088459A1 (en) Method for producing amino trimethylene phosphonic acid as water treatment agent
CN105332058B (en) The method that dissolution method produces gypsum for paper whisker is recycled under ardealite normal pressure
CN1086361C (en) Production technology of yellow flaky sodium sulfide with low carbon and iron contents
CN105271157A (en) Method for comprehensively treating titanium white waste acid and phosphate floatation tailings
CN110028045A (en) Utilize the method for calcium metaborate concentration titanium white waste acid
CN110040698B (en) Method for treating titanium dioxide waste acid by using magnesium sulfate
CN110104616A (en) Utilize the method for sodium tetraborate concentration titanium white waste acid
CN110104617A (en) Utilize the method for alum concentration titanium white waste acid
CN109941970A (en) Utilize the method for aluminum aluminum sulfate concentration titanium white waste acid
CN109987589A (en) Utilize the method for ferric trichloride concentration titanium white waste acid
CN101973530A (en) Method for treating waste titanium dioxide acid
CN102897802B (en) Method for recycling reagent-grade anhydrous sodium sulfate from basic cupric carbonate production waste liquid
CN109941971A (en) Utilize the method for biphosphate Calcium treatment waste sulfuric acid solution
CN108217739A (en) It is a kind of to prepare the method for manganese sulfate and its product obtained with troilite
CN109941969A (en) Utilize the method for disodium hydrogen phosphate processing waste sulfuric acid solution
CN110040697A (en) The processing method of titanium dioxide waste acid by sulfuric acid process
CN109941968A (en) Utilize the method for sodium dihydrogen phosphate processing waste sulfuric acid solution
CN102503812A (en) Method for increasing citric acid yield in extracting process of citric acid with calcium-salt method
CN109987588A (en) Utilize the method for sodium pyrophosphate processing waste sulfuric acid solution
CN110040693A (en) Utilize the method for calcium monohydrogen phosphate processing waste sulfuric acid solution
CN110040695A (en) Utilize the method for trbasic zinc phosphate processing waste sulfuric acid solution
CN110040694A (en) Utilize the method for sodium phosphate processing waste sulfuric acid solution

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
WW01 Invention patent application withdrawn after publication
WW01 Invention patent application withdrawn after publication

Application publication date: 20190719