CN108940553A - A kind of ore crushing grinding aid special - Google Patents

A kind of ore crushing grinding aid special Download PDF

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Publication number
CN108940553A
CN108940553A CN201810797414.XA CN201810797414A CN108940553A CN 108940553 A CN108940553 A CN 108940553A CN 201810797414 A CN201810797414 A CN 201810797414A CN 108940553 A CN108940553 A CN 108940553A
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Prior art keywords
grinding aid
parts
ore
crushes
graphene oxide
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CN201810797414.XA
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CN108940553B (en
Inventor
裘友玖
马俊杰
宋宇星
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Qianxi Fortune Mining Co ltd
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Foshan Ling Chao New Material Co Ltd
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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B02CRUSHING, PULVERISING, OR DISINTEGRATING; PREPARATORY TREATMENT OF GRAIN FOR MILLING
    • B02CCRUSHING, PULVERISING, OR DISINTEGRATING IN GENERAL; MILLING GRAIN
    • B02C23/00Auxiliary methods or auxiliary devices or accessories specially adapted for crushing or disintegrating not provided for in preceding groups or not specially adapted to apparatus covered by a single preceding group
    • B02C23/06Selection or use of additives to aid disintegrating

Abstract

The invention discloses a kind of ores to crush grinding aid special, belongs to technical field of mineral processing.It includes surfactant, ammonium nitrate, inorganic salts, crystallization hydrate, coupling agent, isocyanates and amino graft modification graphene oxide that the ore that the present invention develops, which crushes grinding aid special, surfactant, ammonium nitrate, inorganic salts, crystallization hydrate, coupling agent and amino graft modification graphene oxide are first mixed and are poured into batch mixer by the present invention, and the dehydrated alcohol of 1.0~2.0 times of inorganic salt quality is added, under the conditions of temperature is 10~20 DEG C, after being stirred 2~4h, vacuum freeze drying obtains mixture;Again by mixture and isocyanates under the conditions of temperature is 4~6 DEG C, after being stirred, discharging crushes grinding aid special to get ore.The ore of technical solution of the present invention preparation, which crushes grinding aid special, has the characteristics that excellent grinding efficiency, has broad prospects in the development of mineral processing technology industry.

Description

A kind of ore crushing grinding aid special
Technical field
The invention discloses a kind of ores to crush grinding aid special, belongs to technical field of mineral processing.
Background technique
Grinding process is the very high operation of energy consumption, especially when needing to carry out fine grinding and Ultrafine Grinding to mineral, energy It consumes higher.Statistical result shows that the electric energy of grinding consumption accounts for about the 5% of current year power generation total amount;In investment, grinding operation accounts for whole 60% or so of a dressing plant's investment;The power consumption of grinding operation accounts for about the 30%~70% of full factory's investment, and production and operation expense also accounts for entirely Factory's investment 40%~50%;Technically, main problem existing for grinding operation is exactly energy consumption height, low efficiency.Therefore, ore grinding is reduced The energy consumption of energy consumption, particularly fine grinding and Ultra-fine grinding is of great significance.Adding grinding aid in ore grinding can be to a certain extent Reduce ore grinding energy consumption, the grinding efficiency obtained.Reinforce the research of the mechanism of action of grinding process grinding aid, the choosing to grinding aid It selects and using being of great significance.
The crushing of raw material is an essential process in mineral process, and crush be a high energy consumption, it is inefficient The operation process of rate, such as the levigate power consumption of ceramic industry chats raw material account for about the 2/3 of the total power consumption of full factory of ceramics factory, but efficiency It but is only 1% even lower, most input energy is for generating heat, useless impact, extruding, abrasion, electrostatic energy, bullet Property and plastic deformation and noise.And this is used for 1% electric energy of grinding, and due in grinding process, with the increase of grinding fineness And specific surface area is caused to increase, the adhesion strength or interfacial tension of powder increase with it, and the crack that particle can be made to have generated is cured again It closes, qualified fine powder generates cushion, cut down impact, grinding energy in mill due to that cannot draw off in time;In addition, particle is disconnected Free electrovalent bond when splitting on generated new surface drives adjacent particles to adhere to each other and assemble.It is all these all to seriously affect The mill efficiency of milling equipment, greatly reduces capacity usage ratio.Therefore, raw material fine grinding efficiency is improved, is had to energy-saving Important realistic meaning.Traditional mineral grinding aid generally uses such as sodium carbonate, sodium metasilicate, sodium phosphate inorganic salts, and The inorganic salts of some amines.These grinding aids have preferable grinding-aid effect to a certain extent, but because its sphere of action is limited, It is often only preferable to certain raw material effect.
And traditional ore crushes therefore how the grinding aid special problem bad there is also grinding-aid effect makes mineral powder Broken grinding aid special, which plays better performance, becomes the art one of the technical problems that are urgent to solve.
Summary of the invention
The present invention solves the technical problem of: grinding-aid effect existing for grinding aid special is crushed for traditional ore Bad disadvantage provides a kind of ore crushing grinding aid special.
In order to solve the above-mentioned technical problem, the technical scheme adopted by the invention is that:
A kind of ore crushing grinding aid special, the raw material including following parts by weight:
3~5 parts of surfactant
4~8 parts of ammonium nitrate
30~40 parts of inorganic salts
8~10 parts of hydrate of crystallization
2~3 parts of coupling agent
4~6 parts of isocyanates
8~10 parts of amino graft modification graphene oxide
The ore crushes the process for preparation of grinding aid special are as follows:
(1) each component is weighed by raw material composition;
(2) by surfactant, ammonium nitrate, inorganic salts, crystallization hydrate, coupling agent and amino graft modification graphene oxide Mixing is poured into batch mixer, and the dehydrated alcohol of 1.0~2.0 times of inorganic salt quality is added, under the conditions of temperature is 10~20 DEG C, After being stirred 2~4h, vacuum freeze drying obtains mixture;
(3) by mixture and isocyanates under the conditions of temperature is 4~6 DEG C, after being stirred, discharging crushes special to get ore Use grinding aid.
The surfactant is in neopelex, cetyl trimethylammonium bromide or sodium lignin sulfonate Any one.
The inorganic salts are that aluminium chloride and sodium thiosulfate are that 3:1~10:1 is mixed in mass ratio.
The crystallization hydrate is that Disodium sulfate decahydrate, green vitriol and 12 hydrazine aluminum sulfate potassium press quality Than being compounded for 10:1:1.
The coupling agent is any one in silane coupling agent, aluminate coupling agent or titanate coupling agent.
The isocyanates is toluene di-isocyanate(TDI), methyl diphenylene diisocyanate or trimethyl cyclohexane diisocyanate Any one in ester.
The modifying process of the amino graft modification graphene oxide are as follows: by the dimethyl of graphene oxide and sodium azide Formamide solution is after reaction is mixed in 1:8~1:10, to add 0.4~0.5 times of graphene oxide quality in mass ratio Lithium aluminium hydride reduction continues after being stirred to react, filtering, and washing and drying obtain amino graft modification graphene oxide.
The beneficial effects of the present invention are:
(1) technical solution of the present invention passes through addition ammonium nitrate, inorganic salts, crystallization hydrate, isocyanates and modified oxidized A variety of active principles such as graphene play good grinding-aid effect by mutual synergistic effect;In product use process In, since mechanical lapping can generate a large amount of heat, the heat of generation can be used as " fuse cord " for causing a series of complex reaction, First happens is that the crystallization water in crystallization hydrate is changed into the process of free water, free water generate can in system Isocyanates is contacted and is reacted, and generates carbon dioxide gas, and the generation of gas, which can not only be played, improves body in process of lapping It is the effect of mobility, the reunion again of slag particle can also be effectively avoided in crushing process, to effectively improves grinding Efficiency;In addition the accumulation of the heat generated with grinding, internal local temperature is further up, so as to cause the decomposition of ammonium nitrate And the melting of lower melting-point inorganic salts, wherein ammonium nitrate is decomposed into violent exothermic reaction, can be in a heated condition Explosion type occurs to decompose, to be conducive to the quick disintegration of ore in process of lapping, in addition, the explosion type decomposition of its part can produce Raw certain air pressure further promotes grinding efficiency, wherein fusing point to be conducive to scattering and permeating of the grinding aid in system Lower inorganic salts, i.e. sodium thiosulfate and aluminium chloride can effectively improve the mobility of system after melted by heating, in addition, its Partly because temperature reduces and is covered on the ore particles surface of refinement again after heat loss in transfer process after melting, thus So that the electronic state on solid mineral surface is changed, eliminates or weaken solid particle and form after section that adhesion and aggregation becomes again Gesture reduces a possibility that section heals again, and increases the specific surface area of solid matter, keeps powder granule finer and smoother, separately Outside, the hardness that the absorption package of lower melting-point inorganic salts can lead to mineral particle surface reduces, and is conducive to subsequent process of lapping In further refinement;
(2) technical solution of the present invention aoxidizes stone by the graphene oxide of addition amino graft modification as one of effective component Black alkene can play good lubricant effect during the grinding process, and not only had amino in its structure but also had carboxyl, and no matter is the two Be under acid system or alkaline system, after one of group is ionized, can make graphene oxide layer structure because It is mutually exclusive with like charges, to make its fine dispersion in system, and attract each other with the opposite charges in system, It is set effectively to be adsorbed on abrasive media, milling apparatus surface effectively prevents ore raw materials in abrasive media and milling apparatus table The adherency in face further increases grinding efficiency, promotes grinding yield.
Specific embodiment
In mass ratio it is 1 by the dimethyl formamide solution of sodium azide that graphene oxide and mass fraction are 4~6%: 8~1:10 mixing is poured into reaction kettle, under the conditions of supersonic frequency is 65~70kHz, after 30~40min of ultrasonic disperse, and Yu Wen Degree is 70~85 DEG C, under the conditions of revolving speed is 600~800r/min, after constant temperature is stirred to react 2~3h, adds graphene oxide matter The lithium aluminium hydride reduction of 0.4~0.5 times of amount is 75~85 DEG C in temperature, and under the conditions of revolving speed is 600~800r/min, constant temperature stirring is anti- After answering 3~5h, filtering obtains filter cake, and gained filter cake is dried in vacuo, obtains amino graft modification graphene oxide;By weight Number meter, successively takes 3~5 parts of surfactants, 4~8 parts of ammonium nitrate, 30~40 parts of inorganic salts, 8~10 parts of crystallization hydrates, and 2 ~3 parts of coupling agents, 8~10 parts of amino graft modification graphene oxides, first by surfactant, ammonium nitrate, inorganic salts, the crystallization water Compound, coupling agent and the mixing of amino graft modification graphene oxide are poured into batch mixer, and be added inorganic salt quality 1.0~ 2.0 times of dehydrated alcohol is then 10~20 DEG C in temperature, and under the conditions of revolving speed is 400~600r/min, constant temperature is stirred 2 After~4h, discharging, vacuum freeze drying obtains mixture;Gained mixture and isocyanates are poured into batch mixer again, in temperature It is 4~6 DEG C, under the conditions of revolving speed is 800~1200r/min, after low temperature is stirred 4~6h, discharging crushes dedicated to get ore Grinding aid.The surfactant is in neopelex, cetyl trimethylammonium bromide or sodium lignin sulfonate Any one.The inorganic salts are that aluminium chloride and sodium thiosulfate are that 3:1~10:1 is mixed in mass ratio.The crystallization Hydrate be Disodium sulfate decahydrate, green vitriol and 12 hydrazine aluminum sulfate potassium be in mass ratio 10:1:1 compounding and At.The coupling agent is any one in silane coupling agent, aluminate coupling agent or titanate coupling agent.The isocyanates Any one for toluene di-isocyanate(TDI), in methyl diphenylene diisocyanate or trimethylhexane diisocyanate.
It is in mass ratio 1:10 by the dimethyl formamide solution of sodium azide that graphene oxide and mass fraction are 6% Mixing is poured into reaction kettle, is 85 DEG C in temperature, revolving speed is after ultrasonic disperse 40min under the conditions of supersonic frequency is 70kHz Under the conditions of 800r/min, after constant temperature is stirred to react 3h, 0.5 times of graphene oxide quality of lithium aluminium hydride reduction is added, is in temperature 85 DEG C, under the conditions of revolving speed is 800r/min, after constant temperature is stirred to react 5h, filtering obtains filter cake, and gained filter cake is dried in vacuo, Obtain amino graft modification graphene oxide;According to parts by weight, 5 parts of surfactants are successively taken, 8 parts of ammonium nitrate, 40 parts inorganic Salt, 10 parts of crystallization hydrates, 3 parts of coupling agents, 10 parts of amino graft modification graphene oxides, first by surfactant, nitric acid Ammonium, inorganic salts, crystallization hydrate, coupling agent and the mixing of amino graft modification graphene oxide are poured into batch mixer, and are added The dehydrated alcohol of 2.0 times of inorganic salt quality is then 20 DEG C in temperature, and under the conditions of revolving speed is 600r/min, constant temperature is stirred After 4h, discharging, vacuum freeze drying obtains mixture;Gained mixture and isocyanates are poured into batch mixer again, are in temperature 6 DEG C, under the conditions of revolving speed is 1200r/min, after low temperature is stirred 6h, discharging crushes grinding aid special to get ore.The table Face activating agent is neopelex.The inorganic salts be aluminium chloride and sodium thiosulfate be in mass ratio 10:1 mixing and At.The crystallization hydrate is that Disodium sulfate decahydrate, green vitriol and 12 hydrazine aluminum sulfate potassium are in mass ratio 10:1:1 is compounded.The coupling agent is silane coupling agent.The isocyanates is toluene di-isocyanate(TDI).
According to parts by weight, 5 parts of surfactants, 8 parts of ammonium nitrate, 40 parts of inorganic salts, 10 parts of crystallization hydrates are successively taken Object, 3 parts of coupling agents, 10 parts of graphene oxides, first by surfactant, ammonium nitrate, inorganic salts, crystallization hydrate, coupling agent It is poured into batch mixer with the mixing of amino graft modification graphene oxide, and the dehydrated alcohol of 2.0 times of inorganic salt quality is added, then It is 20 DEG C in temperature, under the conditions of revolving speed is 600r/min, after constant temperature is stirred 4h, discharging, vacuum freeze drying must be mixed Material;Gained mixture and isocyanates are poured into batch mixer again, in temperature be 6 DEG C, revolving speed be 1200r/min under the conditions of, it is low After temperature is stirred 6h, discharging crushes grinding aid special to get ore.The surfactant is neopelex. The inorganic salts are that aluminium chloride and sodium thiosulfate are that 10:1 is mixed in mass ratio.The crystallization hydrate is ten hydrations Sodium sulphate, green vitriol and 12 hydrazine aluminum sulfate potassium are that 10:1:1 is compounded in mass ratio.The coupling agent is Silane coupling agent.The isocyanates is toluene di-isocyanate(TDI).
According to parts by weight, 5 parts of surfactants, 8 parts of ammonium nitrate, 40 parts of inorganic salts, 10 parts of crystallization hydrates are successively taken Object, 3 parts of coupling agents, first by surfactant, ammonium nitrate, inorganic salts, crystallization hydrate, coupling agent and amino graft modification oxygen The mixing of graphite alkene is poured into batch mixer, and the dehydrated alcohol of 2.0 times of inorganic salt quality is added, and is then 20 DEG C in temperature, is turned Under the conditions of speed is 600r/min, after constant temperature is stirred 4h, discharging, vacuum freeze drying obtains mixture;Again by gained mixture Poured into batch mixer with isocyanates, in temperature be 6 DEG C, revolving speed be 1200r/min under the conditions of, after low temperature is stirred 6h, out Material crushes grinding aid special to get ore.The surfactant is neopelex.The inorganic salts are aluminium chloride It is mixed in mass ratio for 10:1 with sodium thiosulfate.The crystallization hydrate is Disodium sulfate decahydrate, seven hydrated sulfuric acids Ferrous and 12 hydrazine aluminum sulfate potassium are that 10:1:1 is compounded in mass ratio.The coupling agent is silane coupling agent.It is described different Cyanate is toluene di-isocyanate(TDI).
It is in mass ratio 1:10 by the dimethyl formamide solution of sodium azide that graphene oxide and mass fraction are 6% Mixing is poured into reaction kettle, is 85 DEG C in temperature, revolving speed is after ultrasonic disperse 40min under the conditions of supersonic frequency is 70kHz Under the conditions of 800r/min, after constant temperature is stirred to react 3h, 0.5 times of graphene oxide quality of lithium aluminium hydride reduction is added, is in temperature 85 DEG C, under the conditions of revolving speed is 800r/min, after constant temperature is stirred to react 5h, filtering obtains filter cake, and gained filter cake is dried in vacuo, Obtain amino graft modification graphene oxide;According to parts by weight, 5 parts of surfactants, 40 parts of inorganic salts, 10 parts of crystallizations are successively taken Hydrate, 3 parts of coupling agents, 10 parts of amino graft modification graphene oxides, first by surfactant, inorganic salts, crystallization aquation It closes object, coupling agent and the mixing of amino graft modification graphene oxide to pour into batch mixer, and the nothing of 2.0 times of inorganic salt quality is added Water-ethanol is then 20 DEG C in temperature, and under the conditions of revolving speed is 600r/min, after constant temperature is stirred 4h, discharging, vacuum refrigeration is done It is dry, obtain mixture;Gained mixture and isocyanates are poured into batch mixer again, in temperature be 6 DEG C, revolving speed 1200r/min Under the conditions of, after low temperature is stirred 6h, discharging crushes grinding aid special to get ore.The surfactant is dodecyl Benzene sulfonic acid sodium salt.The inorganic salts are that aluminium chloride and sodium thiosulfate are that 10:1 is mixed in mass ratio.The crystallization hydrate Object is that Disodium sulfate decahydrate, green vitriol and 12 hydrazine aluminum sulfate potassium are that 10:1:1 is compounded in mass ratio.Institute Stating coupling agent is silane coupling agent.The isocyanates is toluene di-isocyanate(TDI).
It is in mass ratio 1:10 by the dimethyl formamide solution of sodium azide that graphene oxide and mass fraction are 6% Mixing is poured into reaction kettle, is 85 DEG C in temperature, revolving speed is after ultrasonic disperse 40min under the conditions of supersonic frequency is 70kHz Under the conditions of 800r/min, after constant temperature is stirred to react 3h, 0.5 times of graphene oxide quality of lithium aluminium hydride reduction is added, is in temperature 85 DEG C, under the conditions of revolving speed is 800r/min, after constant temperature is stirred to react 5h, filtering obtains filter cake, and gained filter cake is dried in vacuo, Obtain amino graft modification graphene oxide;According to parts by weight, 5 parts of surfactants are successively taken, 8 parts of ammonium nitrate, 40 parts inorganic Salt, 10 parts of crystallization hydrates, 3 parts of coupling agents, 10 parts of amino graft modification graphene oxides, first by surfactant, nitric acid Ammonium, inorganic salts, crystallization hydrate, coupling agent and the mixing of amino graft modification graphene oxide are poured into batch mixer, and are added The dehydrated alcohol of 2.0 times of inorganic salt quality is then 20 DEG C in temperature, and under the conditions of revolving speed is 600r/min, constant temperature is stirred After 4h, discharging, vacuum freeze drying obtains mixture;Gained mixture is poured into batch mixer again, is 6 DEG C in temperature, revolving speed is Under the conditions of 1200r/min, after low temperature is stirred 6h, discharging crushes grinding aid special to get ore.The surfactant is Neopelex.The inorganic salts are that aluminium chloride and sodium thiosulfate are that 10:1 is mixed in mass ratio.The knot Brilliant hydrate is that Disodium sulfate decahydrate, green vitriol and 12 hydrazine aluminum sulfate potassium are 10:1:1 compounding in mass ratio It forms.The coupling agent is silane coupling agent.
It is in mass ratio 1:10 by the dimethyl formamide solution of sodium azide that graphene oxide and mass fraction are 6% Mixing is poured into reaction kettle, is 85 DEG C in temperature, revolving speed is after ultrasonic disperse 40min under the conditions of supersonic frequency is 70kHz Under the conditions of 800r/min, after constant temperature is stirred to react 3h, 0.5 times of graphene oxide quality of lithium aluminium hydride reduction is added, is in temperature 85 DEG C, under the conditions of revolving speed is 800r/min, after constant temperature is stirred to react 5h, filtering obtains filter cake, and gained filter cake is dried in vacuo, Obtain amino graft modification graphene oxide;According to parts by weight, 5 parts of surfactants, 8 parts of ammonium nitrate, 10 parts of crystallizations are successively taken Hydrate, 3 parts of coupling agents, 10 parts of amino graft modification graphene oxides, first by surfactant, ammonium nitrate, crystallization aquation It closes object, coupling agent and the mixing of amino graft modification graphene oxide to pour into batch mixer, and dehydrated alcohol is added, then in temperature It is 20 DEG C, under the conditions of revolving speed is 600r/min, after constant temperature is stirred 4h, discharging, vacuum freeze drying obtains mixture;Again will Gained mixture and isocyanates pour into batch mixer, are 6 DEG C in temperature, under the conditions of revolving speed is 1200r/min, low temperature stirring is mixed After closing 6h, discharging crushes grinding aid special to get ore.The surfactant is neopelex.The crystallization Hydrate be Disodium sulfate decahydrate, green vitriol and 12 hydrazine aluminum sulfate potassium be in mass ratio 10:1:1 compounding and At.The coupling agent is silane coupling agent.The isocyanates is toluene di-isocyanate(TDI).
It is in mass ratio 1:10 by the dimethyl formamide solution of sodium azide that graphene oxide and mass fraction are 6% Mixing is poured into reaction kettle, is 85 DEG C in temperature, revolving speed is after ultrasonic disperse 40min under the conditions of supersonic frequency is 70kHz Under the conditions of 800r/min, after constant temperature is stirred to react 3h, 0.5 times of graphene oxide quality of lithium aluminium hydride reduction is added, is in temperature 85 DEG C, under the conditions of revolving speed is 800r/min, after constant temperature is stirred to react 5h, filtering obtains filter cake, and gained filter cake is dried in vacuo, Obtain amino graft modification graphene oxide;According to parts by weight, 5 parts of surfactants are successively taken, 8 parts of ammonium nitrate, 40 parts inorganic Salt, 3 parts of coupling agents, 10 parts of amino graft modification graphene oxides, first by surfactant, ammonium nitrate, inorganic salts, coupling agent and The mixing of amino graft modification graphene oxide is poured into batch mixer, and the dehydrated alcohol of 2.0 times of inorganic salt quality is added, then in Temperature is 20 DEG C, and under the conditions of revolving speed is 600r/min, after constant temperature is stirred 4h, discharging, vacuum freeze drying obtains mixture; Gained mixture and isocyanates are poured into batch mixer again, are 6 DEG C in temperature, under the conditions of revolving speed is 1200r/min, low temperature is stirred After mixing mixing 6h, discharging crushes grinding aid special to get ore.The surfactant is neopelex.It is described Inorganic salts are that aluminium chloride and sodium thiosulfate are that 10:1 is mixed in mass ratio.The coupling agent is silane coupling agent.It is described Isocyanates is toluene di-isocyanate(TDI).
Comparative example: the ore of Jinhua material production Co., Ltd production crushes grinding aid special.
Example 1 to the resulting ore of example 7 is crushed into grinding aid special and comparative example product carries out performance detection, it is specific to examine Survey method is as follows:
Test specimen is calculated according to 100% purity, is added in speed muller with different additional amount and quartz, talcum, zircon etc. Natural mineral raw is ground together, the ratio of control material, ball, water when grinding are as follows: material: ball: water=1:2:1, is used after grinding 5min 200 mesh sieves, with a ten thousandth electronic balance weighing drying after tailing over, using tail over number as measurement grinding effect it is excellent Bad index.The grinding efficiency increase rate of grinding aid is calculated using formula (1).
Formula (1): E=[(R0-R1) ÷ R0】×100%
E is grinding efficiency increase rate, % in formula.R0Not add screen over-size when grinding aid, %;R1Tailing over when for grinding aid is added Amount, %.
Specific testing result is as shown in table 1:
1 ore of table crushes the specific testing result of grinding aid special
It is found that the ore of technical solution of the present invention preparation crushes grinding aid special there is excellent grinding to imitate by 1 testing result of table The characteristics of rate, has broad prospects in the development of mineral processing technology industry.

Claims (7)

1. a kind of ore crushes grinding aid special, which is characterized in that the raw material including following parts by weight:
3~5 parts of surfactant
4~8 parts of ammonium nitrate
30~40 parts of inorganic salts
8~10 parts of hydrate of crystallization
2~3 parts of coupling agent
4~6 parts of isocyanates
8~10 parts of amino graft modification graphene oxide
The ore crushes the process for preparation of grinding aid special are as follows:
(1) each component is weighed by raw material composition;
(2) by surfactant, ammonium nitrate, inorganic salts, crystallization hydrate, coupling agent and amino graft modification graphene oxide Mixing is poured into batch mixer, and the dehydrated alcohol of 1.0~2.0 times of inorganic salt quality is added, under the conditions of temperature is 10~20 DEG C, After being stirred 2~4h, vacuum freeze drying obtains mixture;
(3) by mixture and isocyanates under the conditions of temperature is 4~6 DEG C, after being stirred, discharging crushes special to get ore Use grinding aid.
2. a kind of ore according to claim 1 crushes grinding aid special, which is characterized in that the surfactant is ten Any one in dialkyl benzene sulfonic acids sodium, cetyl trimethylammonium bromide or sodium lignin sulfonate.
3. a kind of ore according to claim 1 crushes grinding aid special, which is characterized in that the inorganic salts are aluminium chloride It is in mass ratio that 3:1~10:1 is mixed with sodium thiosulfate.
4. a kind of ore according to claim 1 crushes grinding aid special, which is characterized in that the crystallization hydrate is Disodium sulfate decahydrate, green vitriol and 12 hydrazine aluminum sulfate potassium are that 10:1:1 is compounded in mass ratio.
5. a kind of ore according to claim 1 crushes grinding aid special, which is characterized in that the coupling agent is that silane is even Join any one in agent, aluminate coupling agent or titanate coupling agent.
6. a kind of ore according to claim 1 crushes grinding aid special, which is characterized in that the isocyanates is toluene Any one in diisocyanate, methyl diphenylene diisocyanate or trimethylhexane diisocyanate.
7. a kind of ore according to claim 1 crushes grinding aid special, which is characterized in that the amino graft modification oxygen The modifying process of graphite alkene are as follows: the dimethyl formamide solution by graphene oxide and sodium azide be in mass ratio 1:8~ After reaction is mixed in 1:10,0.4~0.5 times of graphene oxide quality of lithium aluminium hydride reduction is added, is continued after being stirred to react, mistake Filter, washing and drying, obtain amino graft modification graphene oxide.
CN201810797414.XA 2018-07-19 2018-07-19 Grinding aid special for ore crushing Expired - Fee Related CN108940553B (en)

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* Cited by examiner, † Cited by third party
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CN109859879A (en) * 2019-03-06 2019-06-07 毛红玲 A kind of high-performance conductive film and its processing method based on graphene
CN111250252A (en) * 2019-12-30 2020-06-09 浙江瑞堂塑料科技股份有限公司 Grinding aid for thermoplastic grinding process and grinding equipment
CN112592098A (en) * 2020-12-24 2021-04-02 泰安市同达建材有限公司 Concrete modifying flexibilizer and preparation method thereof
CN113636777A (en) * 2020-04-27 2021-11-12 南京神仂建材科技有限公司 Slag grinding aid and preparation method thereof

Citations (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101708970A (en) * 2009-05-26 2010-05-19 湖北统领科技有限公司 Low-alkali composite multi-functional cement grinding aid and preparation method thereof
CN102001840A (en) * 2010-12-10 2011-04-06 甘肃省建材科研设计院 Powder composite cement grinding additive and preparation method thereof
CN102976650A (en) * 2012-12-04 2013-03-20 山东宏艺科技股份有限公司 Set-retarding grinding aid for set-retarding cement and preparation method of set-retarding grinding aid
CN103265223A (en) * 2013-06-03 2013-08-28 东南大学 Cement grinding aid
CN103332670A (en) * 2013-06-21 2013-10-02 重庆交通大学 Method for preparing graphene oxide
CN103949218A (en) * 2014-04-21 2014-07-30 华南理工大学 Modified graphene adsorbent as well as preparation method and application thereof
CN102311242B (en) * 2011-05-27 2014-10-01 刘长福 Water-soluble polymer grinding aid prepared from papermaking waste liquor and preparation method thereof
CN104743952A (en) * 2015-03-11 2015-07-01 南京工业大学 Activation grinding aid used for grinding of high titanium slag powder and preparation method of activation grinding aid
CN105110689A (en) * 2015-07-23 2015-12-02 柳州博泽科技有限公司 Cement grinding aid, and preparation method thereof
CN105130253A (en) * 2015-09-18 2015-12-09 广西路佳道桥勘察设计有限公司 Novel cement grinding aid and cement employing same
CN105198271A (en) * 2015-10-28 2015-12-30 徐福明 Cement grinding aid and preparation method thereof
CN105694461A (en) * 2015-12-14 2016-06-22 上海应用技术学院 Graphene oxide-modified silicone rubber composite and preparation method thereof
CN106277894A (en) * 2016-09-05 2017-01-04 陈小华 A kind of environmental protection early-strength graphene oxide cement grinding aid and preparation method thereof
CN106673479A (en) * 2016-10-25 2017-05-17 广东弘朝科技有限公司 Cement grinding aid used for gangue
CN107235649A (en) * 2017-05-17 2017-10-10 常州第六元素材料科技股份有限公司 A kind of cement grinding aid and preparation method thereof
CN107497404A (en) * 2017-10-18 2017-12-22 中南林业科技大学 A kind of preparation method of modified graphene oxide sorbing material
CN107935427A (en) * 2017-11-21 2018-04-20 常州市奥普泰科光电有限公司 A kind of composite steel slag grinding aid

Patent Citations (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101708970A (en) * 2009-05-26 2010-05-19 湖北统领科技有限公司 Low-alkali composite multi-functional cement grinding aid and preparation method thereof
CN102001840A (en) * 2010-12-10 2011-04-06 甘肃省建材科研设计院 Powder composite cement grinding additive and preparation method thereof
CN102311242B (en) * 2011-05-27 2014-10-01 刘长福 Water-soluble polymer grinding aid prepared from papermaking waste liquor and preparation method thereof
CN102976650A (en) * 2012-12-04 2013-03-20 山东宏艺科技股份有限公司 Set-retarding grinding aid for set-retarding cement and preparation method of set-retarding grinding aid
CN103265223A (en) * 2013-06-03 2013-08-28 东南大学 Cement grinding aid
CN103332670A (en) * 2013-06-21 2013-10-02 重庆交通大学 Method for preparing graphene oxide
CN103949218A (en) * 2014-04-21 2014-07-30 华南理工大学 Modified graphene adsorbent as well as preparation method and application thereof
CN104743952A (en) * 2015-03-11 2015-07-01 南京工业大学 Activation grinding aid used for grinding of high titanium slag powder and preparation method of activation grinding aid
CN105110689A (en) * 2015-07-23 2015-12-02 柳州博泽科技有限公司 Cement grinding aid, and preparation method thereof
CN105130253A (en) * 2015-09-18 2015-12-09 广西路佳道桥勘察设计有限公司 Novel cement grinding aid and cement employing same
CN105198271A (en) * 2015-10-28 2015-12-30 徐福明 Cement grinding aid and preparation method thereof
CN105694461A (en) * 2015-12-14 2016-06-22 上海应用技术学院 Graphene oxide-modified silicone rubber composite and preparation method thereof
CN106277894A (en) * 2016-09-05 2017-01-04 陈小华 A kind of environmental protection early-strength graphene oxide cement grinding aid and preparation method thereof
CN106673479A (en) * 2016-10-25 2017-05-17 广东弘朝科技有限公司 Cement grinding aid used for gangue
CN107235649A (en) * 2017-05-17 2017-10-10 常州第六元素材料科技股份有限公司 A kind of cement grinding aid and preparation method thereof
CN107497404A (en) * 2017-10-18 2017-12-22 中南林业科技大学 A kind of preparation method of modified graphene oxide sorbing material
CN107935427A (en) * 2017-11-21 2018-04-20 常州市奥普泰科光电有限公司 A kind of composite steel slag grinding aid

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109859879A (en) * 2019-03-06 2019-06-07 毛红玲 A kind of high-performance conductive film and its processing method based on graphene
CN111250252A (en) * 2019-12-30 2020-06-09 浙江瑞堂塑料科技股份有限公司 Grinding aid for thermoplastic grinding process and grinding equipment
CN111250252B (en) * 2019-12-30 2021-07-09 浙江瑞堂塑料科技股份有限公司 Grinding aid for thermoplastic grinding process and grinding equipment
CN113636777A (en) * 2020-04-27 2021-11-12 南京神仂建材科技有限公司 Slag grinding aid and preparation method thereof
CN112592098A (en) * 2020-12-24 2021-04-02 泰安市同达建材有限公司 Concrete modifying flexibilizer and preparation method thereof

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