CN103316776A - Sulfonated soap and preparation method thereof - Google Patents

Sulfonated soap and preparation method thereof Download PDF

Info

Publication number
CN103316776A
CN103316776A CN2013102262729A CN201310226272A CN103316776A CN 103316776 A CN103316776 A CN 103316776A CN 2013102262729 A CN2013102262729 A CN 2013102262729A CN 201310226272 A CN201310226272 A CN 201310226272A CN 103316776 A CN103316776 A CN 103316776A
Authority
CN
China
Prior art keywords
soap
preparation
sulfonation
november
grade
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
CN2013102262729A
Other languages
Chinese (zh)
Inventor
田清源
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.)
Guangping Shangyuan Ore Dressing Auxiliaries Co Ltd
Original Assignee
Guangping Shangyuan Ore Dressing Auxiliaries 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 Guangping Shangyuan Ore Dressing Auxiliaries Co Ltd filed Critical Guangping Shangyuan Ore Dressing Auxiliaries Co Ltd
Priority to CN2013102262729A priority Critical patent/CN103316776A/en
Publication of CN103316776A publication Critical patent/CN103316776A/en
Pending legal-status Critical Current

Links

Landscapes

  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

The invention discloses a sulfonated soap and a preparation method thereof. The preparation method includes: mixing 50% of high-iodine plant oil, 10% of sulfoacid, 8% of sodium hydroxide and 32% of water, heating the mixture to the temperature of 60 DEG C to obtain the sulfonated soap. The content of organic acid in the sulfonated soap prepared by the method is 38%. The problem of low grade and high energy consumption of selected lithium concentrate can be solved, and the problem that beneficiation cannot be performed under low temperature can be solved.

Description

A kind of sulfonation soap and preparation method thereof
Technical field
What the present invention relates to is a kind of sulfonation soap and preparation method thereof (model T-3 soap).
Background technology
Select that the lithium concentrate grade is low, high energy consumption, existing chemical concentration is slow, resistance to low temperature is relatively poor, and concentrate grade and yield are lower.
Therefore, there is defective in prior art, needs to improve.
Summary of the invention
Technical problem to be solved by this invention is to provide a kind of sulfonation soap and preparation method thereof for the deficiencies in the prior art.
Technical scheme of the present invention is as follows:
A kind of preparation method of sulfonation soap according to percentage by weight, adds high iodine number vegetable oil 50%, 10% sulfonic acid, 8% NaOH, 32% water, heats 60 degrees centigrade, the sulfonation soap.
The sulfonation soap of described preparation method's preparation, organic acid content is 38%.
This product selects the phosphorus yield up to monthly average casting yield 95% at the Fanshan, Hebei Province phosphorus ore.Solved the serious problem of ore deposit loss of running.Safe and sound lithium industry company brings up to existing concentrate grade more than 5.5% from former concentrate grade 4.6% in Sichuan.Solved the problem of selecting the high consumption of the low high energy of lithium concentrate grade.And solved the problem that low temperature can not ore dressing.
The specific embodiment
Below in conjunction with specific embodiment, the present invention is described in detail.
Production equipment: one of 02 boiler furnace, one of ten tons of reactor, factory building 50 square meters, water power is complete, one in pond, ten tons of ground.The product processes flow process: add first high iodine number vegetable oil 50%, 10% sulfonic acid, 8% NaOH, 32% water is heated 60 degrees centigrade, the sulfonation soap, organic acid content is 38%.
This product can improve the concentrate grade of product, reduces tailings grade, and gas release is large, and load force is strong, and final pH value is 8.3.
Table 1 product quality indicator
Figure BDA00003321949600021
Annotate: in iron ore, phosphorus ore and lithium ore deposit ore dressing process, can not use separately this product.Existing best proportioning, sulfonation soap (being this product): oxidized paraffin wax soap 6:1 namely gets both sulphonated oxidized paraffinum sodium salts to be developed of the Ministry of Chemical Industry.
Two goldenrain trees are built dragon and select phosphorus collecting agent T-3 laboratory report (proof sulfonation soap has improved concentrate grade and the rate of recovery of selecting phosphorus)
T-3 is a kind of novel phosphorus collecting agent that selects, and in order to verify the character of T-3, gets two Luans and builds Long Shunda to select two the serial flotation in phosphorus workshop be raw material to the ore deposit, take alkali as the ph conditioning agent, waterglass is as inhibitor, tests.
Original ore property: raw ore is phosphorous 2.60%, granularity 31.42%;
Test medicine: collecting agent is T-3 soap (concentration 10%); Foaming agent is activation calcium (concentration 1%); The ph conditioning agent is Na 2CO 3(concentration 5%); Inhibitor is waterglass (concentration 10%);
Testing equipment: roughly select and select the 1L of laboratory flotation device; The selected 0.5L of the laboratory flotation device of selecting;
Conclusion (of pressure testing): 1, Guangping, Hebei Shang Yuan: sulfonation soap: paraffin soap: activation calcium: MES<6:2:1:0.5〉with Handan capric acid leftover bits and pieces soap: paraffin soap: MES<5:4:1〉and Hubei W-1: sulfonation soap: MES<5:4:1〉be respectively laboratory's contrast test of collecting agent at raw ore<Hanyuan phosphorus stone grade is that 5.01%<decimal is disregarded condition under, still medicament closed-circuit test in source has been obtained concentrate grade 36%, tailings grade 0.4%, the sorting index of the rate of recovery 92%.Handan soap closed-circuit test has been obtained concentrate grade 27%, tailings grade 1.8%, and the selection index of the rate of recovery 64%, Hubei W-1 closed-circuit test is obtained concentrate grade 33%, tailings grade 0.9%, the selection index of the rate of recovery 82%.(MES, namely surfactant is commonly called as foaming agent)
2, this test sample ore former grade be 5.01%<by 5%, approximately lower by about 3% than the former grade of normal sample ore, namely floating elaboration position and the rate of recovery are all low.
3, Bench test shows, to compare concentrate grade high by 9% with Handan leftover bits and pieces soap take Handan sulfonation soap as collecting agent, and the rate of recovery is high by 28%, and to compare concentrate grade high by 3% with Hubei W-1, and the rate of recovery is high by 10%
It is single that table 2 pair goldenrain tree is built the first phase output comparison of imperial mining industry Co., Ltd
Unit Time Proportioning Output (ton) Remarks
Lianyun Harbour medicament factory Zero point November 2 6:02:02 96 ?
(TP-2: paraffin soap: MES) On November 28 point 6:02:02 95 ?
? On November 2 16 point 6:02:02 120 ?
? Zero point November 3 6:02:02 101 ?
? On November 38 point 6:02:02 103 ?
? On November 3 16 point 6:02:02 111 ?
? Zero point November 3 6:02:02 120 ?
The Guangping is source medicament factory still On November 48 point 10:02:02 135 ?
(T-3: paraffin soap: MES) On November 4 16 point 10:02:02 115 ?
? Zero point November 4 10:02:02 124 ?
? On November 58 point 10:02:02 124 ?
? On November 5 16 point 10:02:02 130 ?
? Zero point November 5 10:02:02 133 ?
? On November 68 point 10:02:02 118 ?
? On November 6 16 point 10:02:02 136 ?
? Zero point November 6 10:02:02 148 ?
Handan medicament factory On November 78 point 6:02:02 110 ?
(JP-2: paraffin soap: MES) On November 7 16 point 6:02:02 118 ?
? Zero point November 7 6:02:02 125 ?
? On November 88 point 6:02:02 130 ?
? On November 8 16 point 6:02:02 118 ?
? Zero point November 8 6:02:02 104 ?
Annotate: the sulfonation soap of upper table explanation Guangping Shang Yuan is compared with Lianyun Harbour medicament, Handan medicament, and product recovery rate is higher.And concentrate grade adds up to 36.67% the end of the year, is higher than market average 34%.
Anshan iron and steel selects iron collecting agent T-3 laboratory report (proof sulfonation soap improved concentrate grade and the rate of recovery of selecting iron) test medicine, equipment, flow process the same;
Conclusion (of pressure testing): 1, Handan sulfonation soap: tall oil (9:1) and R98-1: tall oil (3:1) and oxidized paraffin wax soap: tall oil (3:1) is respectively laboratory's contrast test of collecting agent, be under 29.53% the condition at head grade, Handan sulfonation soap closed-circuit test has been obtained concentrate grade 58.75%, tailings grade 13.22%, the sorting index of the rate of recovery 71.26%.The R98-1 closed-circuit test has been obtained concentrate grade 58.19%, tailings grade 13.61%, the sorting index of the rate of recovery 70.37%.The oxidized paraffin wax soap closed-circuit test has been obtained concentrate grade 58.96%, tailings grade 13.41%, the sorting index of the rate of recovery 70.66%.
2, the former grade of this test sample ore is 29.53%, and is approximately lower by about 1.5% than normal sample ore original, makes test index lower, and namely floating elaboration position and the rate of recovery are all low.
3, Bench test shows, take Handan sulfonation soap as collecting agent, compares concentrate grade with R98-1 high by 0.56%, and the rate of recovery is high by 0.89%; Compare concentrate grade with oxidized paraffin wax soap low by 0.21%, the rate of recovery is high by 0.60%.
Comprehensive above-mentioned test: this product is mainly used in the flotation at low temperature of metallic ore, nonmetallic ore, has now made Anshan Iron, two Luans, Chengde, alum mountain phosphorus ore etc. all obtain unprecedented benefit.
Should be understood that, for those of ordinary skills, can be improved according to the above description or conversion, and all these improvement and conversion all should belong to the protection domain of claims of the present invention.

Claims (2)

1. the preparation method of a sulfonation soap is characterized in that, according to percentage by weight, adds high iodine number vegetable oil 50%, 10% sulfonic acid, 8% NaOH, 32% water, heats 60 degrees centigrade, the sulfonation soap.
2. the sulfonation soap of preparation method's preparation according to claim 1 is characterized in that, organic acid content is 38%.
CN2013102262729A 2013-06-08 2013-06-08 Sulfonated soap and preparation method thereof Pending CN103316776A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN2013102262729A CN103316776A (en) 2013-06-08 2013-06-08 Sulfonated soap and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN2013102262729A CN103316776A (en) 2013-06-08 2013-06-08 Sulfonated soap and preparation method thereof

Publications (1)

Publication Number Publication Date
CN103316776A true CN103316776A (en) 2013-09-25

Family

ID=49185988

Family Applications (1)

Application Number Title Priority Date Filing Date
CN2013102262729A Pending CN103316776A (en) 2013-06-08 2013-06-08 Sulfonated soap and preparation method thereof

Country Status (1)

Country Link
CN (1) CN103316776A (en)

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4545939A (en) * 1983-07-01 1985-10-08 Lion Corporation Process for producing sulfonate of unsaturated fatty acid ester
US20100021370A1 (en) * 2008-07-25 2010-01-28 Devarayasamudram Ramachandran Nagaraj Flotation Reagents and Flotation Processes Utilizing Same
CN101704769A (en) * 2009-11-19 2010-05-12 贵州大学 Hydrogenated jatropha seed oil fatty acid methyl ester sulfonate prepared by using chlorosulfonic acid as sulfonating agent and preparation method thereof
CN102179311A (en) * 2011-03-16 2011-09-14 内蒙古包钢稀土林峰科技有限公司 Anion collecting agent prepared from illegal cooking oil

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4545939A (en) * 1983-07-01 1985-10-08 Lion Corporation Process for producing sulfonate of unsaturated fatty acid ester
US20100021370A1 (en) * 2008-07-25 2010-01-28 Devarayasamudram Ramachandran Nagaraj Flotation Reagents and Flotation Processes Utilizing Same
CN101704769A (en) * 2009-11-19 2010-05-12 贵州大学 Hydrogenated jatropha seed oil fatty acid methyl ester sulfonate prepared by using chlorosulfonic acid as sulfonating agent and preparation method thereof
CN102179311A (en) * 2011-03-16 2011-09-14 内蒙古包钢稀土林峰科技有限公司 Anion collecting agent prepared from illegal cooking oil

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
余侃萍等: "铁矿反浮选脱磷捕收剂分子设计及其作用机理", 《中国有色金属学报》 *
田爱华: "用植物油研制磷矿浮选剂初探", 《中国优秀硕士学位论文全文数据库工程科技Ⅰ辑》 *
罗惠华等: "胶磷矿选矿中不同植物脂肪酸的常温浮选性能", 《武汉工程大学学报》 *

Similar Documents

Publication Publication Date Title
CN101797536B (en) Collophanite flotation collector and method for preparing same
CN103241966B (en) Clinker free regenerated slag micro-powder compound cement
CN106116295A (en) A kind of frost-resistant concrete
CN205193558U (en) Water electrolytic hydrogen production's hydrogen, oxygen separator protection device
CN101318845A (en) Process for preparing potash magnesium sulphate fertilizer with kalium containing sulfate
CN101837958A (en) Preparation method of high temperature stability insoluble sulfur
CN106269286B (en) Preparation method of sulfonated fatty acid phosphate reverse flotation collector
CN105502303A (en) Production process for preparing insoluble sulfur high in thermal stability and content
CN104399592A (en) Fluorite floatation process
CN107522433A (en) Biomass ash dreg concrete building block and preparation method thereof
CN103265223A (en) Cement grinding aid
CN104372413A (en) Preparation method of calcium sulfate whiskers
CN104451202B (en) Two-stage curing vanadium extraction method of stone coal vanadium ores
CN103316776A (en) Sulfonated soap and preparation method thereof
CN101590450A (en) A kind of preparation method of mineral inhibitor for barite
CN103435376A (en) Method and apparatus used for preparing ammonium phosphate fertilizer from phosphoric acid sediment
CN105195334B (en) Magnesium-rich silicate mineral flotation inhibitor and preparation method and application thereof
CN104475263B (en) Fluorite ore flotation collecting agent
CN106171093A (en) A kind of ardealite and the method in desulfurated plaster improved coordination salt-soda soil
CN202954017U (en) Device for regulating H/C ratio of synthesis gas
CN103357510B (en) Cellophane positive flotation collector and preparation method of cellophane positive flotation collector
CN208413869U (en) A kind of boron trifluoride process units
CN201567228U (en) Ammonia decomposition pressure swing adsorption hydrogen production tail gas recovery device
CN204504566U (en) Magnetic orbit device is used in a kind of spherical storage tank Spherical Tank Shell Plates blanking cutting
CN204138439U (en) Filtering device special for mine water

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C12 Rejection of a patent application after its publication
RJ01 Rejection of invention patent application after publication

Application publication date: 20130925