CN104340968A - Method for removing impurities SiO2 and Al2O3 and purifying graphite - Google Patents

Method for removing impurities SiO2 and Al2O3 and purifying graphite Download PDF

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Publication number
CN104340968A
CN104340968A CN201310315890.0A CN201310315890A CN104340968A CN 104340968 A CN104340968 A CN 104340968A CN 201310315890 A CN201310315890 A CN 201310315890A CN 104340968 A CN104340968 A CN 104340968A
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China
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graphite
normal pressure
concentration
weight
purification
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CN201310315890.0A
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王志敏
刘天云
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QINGDAO GUANGXING ELECTRONIC MATERIALS CO Ltd
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QINGDAO GUANGXING ELECTRONIC MATERIALS CO Ltd
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Priority to CN201310315890.0A priority Critical patent/CN104340968A/en
Publication of CN104340968A publication Critical patent/CN104340968A/en
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Abstract

The present invention provides a method for removing impurities SiO2 and Al2O3 and purifying graphite, wherein impurities in the graphite can be effectively removed through the method, the graphite is adopted as a raw material, the residual SiO2 content in the purified graphite is less than or equal to 30 MG/L, the residual Al2O3 content in the purified graphite is less than or equal to 0.3%, and the purity is more than 99.99%. According to the method, graphite with the carbon content of more than 65% is taken and placed into a reaction kettle I, pressurization alkali leaching and normal pressure acid leaching are adopted to treat the graphite, the concentration of the used LiCO3 is 10-35%, the concentration of the KOH is 6-30%, the concentration of the NaHCO3 is 7-28%, the normal pressure acid leaching is performed under the ultrasonic wave field or/and the microwave field, 21-24% (calculated as the weight of the graphite) by weight of sulfuric acid and 13-28% (calculated as the weight of the graphite) by weight of hydrofluoric acid are added to the treated graphite powder to carry out leaching, the obtained mixture is added to a reaction kettle, stirring heating is performed, cerium carbonate is added, an oxidizing agent is added slowly, and stirring, heating boiling, standing clarification and filtration are performed so as to obtain the high purity graphite with no silicon and aluminum impurities.

Description

A kind of removal impurity SiO 2and Al 2o 3the method of purification graphite
Technical field
The present invention relates to a kind of removal impurity SiO 2and Al 2o 3the method of purification graphite, purification purity is greater than the method for the high purity graphite of 99.99%.
Background technology
High purity graphite is the graphite of content of graphite more than 99.99%, and it is a kind of non-renewable strategic resource, is important war preparedness resource indispensable in military project and modern crafts and hi-tech development always.
The production method of current high purity graphite is mainly based on the wet-process purification method of flotation process, acid-base method, hydrogen fluoride with based on the pyrogenic process method of purification of chlorinating roasting and pyroprocess.There is the deficiencies such as impurity-eliminating effect difference, energy consumption is high, environmental pollution is serious more or less in this several production method.Impurity SiO in graphite 2and Al 2o 3be modal, how thoroughly remove, can reduce costs again, alleviating environmental pollution is current problem demanding prompt solution.
Summary of the invention
The invention provides a kind of removal impurity SiO 2and Al 2o 3the method of purification graphite, effectively can remove the impurity in graphite, makes the content of the fixed carbon of graphite reach 99.99%, reaches the method for high purity graphite requirement.The better performances of product, its technique is simple, advanced, easy handling, and production efficiency is high, facility investment is few, energy consumption is low, and smaller on the impact of environment, cost is low, and graphite products purity is high, can meet the requirement of high purity graphite.
Solving the technical scheme that technical problem of the present invention adopts is: 1. the graphite adopting carbon content > 65% is raw material, after purifying, make SIO 2residual quantity≤28MG/L, AL 2o 3residual quantity≤0.2%, purity > 99.99%, step is as follows: the graphite 500-600kg getting carbon content > 65%, puts into reactor I, alkaline pressure of oxygen leaching and normal pressure acidleach is first adopted to process graphite, LiCO used 3concentration is 10% ~ 35%, KOH concentration is 6% ~ 30%, NaHCO 3concentration is 7% ~ 28%; Wherein normal pressure acidleach is at ultrasonic wave field or/and carry out under microwave field, Graphite Powder 99 after process adds sulfuric acid 21%-24% by the weight percent of graphite again, hydrofluoric acid 13%-28% leaches, join in reactor, stirring heating adds cerous carbonate, is slowly added by oxygenant, stirs, heated and boiled, leave standstill clarification, filter, highly purified graphite can be obtained.
2. the weight liquid-solid ratio of alkaline pressure of oxygen leaching is 1 ~ 9: 1, and temperature is 150 ~ 280 DEG C, and the treatment time is 1 ~ 11 hour; Adopt lime as reagent reclaiming alkali lye.
3. wherein normal pressure acidleach is at ultrasonic wave field or/and carry out under microwave field; Graphite Powder 99 after process adds sulfuric acid 21%-24% by the weight percent of graphite again, hydrofluoric acid 13%-28% leaches, and obtains highly purified graphite products.The weight liquid-solid ratio of normal pressure acidleach is 1 ~ 9:1, and temperature is 35 ~ 85 DEG C, and the treatment time is 2h ~ 90h.
4. ultrasonic frequency range during normal pressure acidleach is at 20 ~ 70KHz, and microwave field range of frequency is at 280GHz ~ 5GHz.
5, graphite is joined in reactor, be heated with stirring to 75-85 DEG C, cerous carbonate is added in the 2-4% ratio of feed liquid TREO amount, by the amount of the 1-1.5% of TREO, oxygenant is slowly added afterwards, stir, heated and boiled more than 35 minutes, leave standstill clarification more than 10 hours, extract the feed liquid of supernatant liquor and band slag respectively, filter.
Above-mentioned alkaline pressure of oxygen leaching: the graphite after ore dressing drops in compressive reaction still, adds alkaline solution, controls reaction conditions, the impurity in graphite and alkali lye are reacted.After reaction terminates, realize solid-liquid separation.Solid adopts pure water to pH=7, and liquid adopts lime to carry out
Above-mentioned normal pressure acidleach: washing mixes to neutral graphite with the acid solution of above-mentioned condition sizes mixing, and controls reaction conditions, the impurity in graphite is reacted with acid further.Reaction process is carried out in ultrasonic wave field or microwave field.The acid waste water produced in washing process and alkaline waste water neutralize mutually, and add the F-in lime precipitation solution.Water after neutralization returns to system and washs.Whole technological process is free from environmental pollution.
The invention has the beneficial effects as follows: graphite obtains high purity graphite after alkaline pressure of oxygen leaching, acidleach process, and adds ultrasonic wave field or microwave field in acidleach process.Technical process is short, easily realizes suitability for industrialized production, and equipment is simple, and security is good, and energy consumption is low, and production cost is low, and environmental pollution is little; In the high purity graphite obtained, the content of fixed carbon is greater than 99.99%.By further purification, can obtain without silicon, the highly purified graphite of aluminium impurity.
Embodiment
Below by embodiment, the present invention is described in further detail.
Embodiment one
Get the graphite 500kg of carbon content > 65%, put into reactor I, first adopt alkaline pressure of oxygen leaching and normal pressure acidleach to process graphite, LiCO used 3concentration is 10%, KOH concentration is 6%, NaHCO 3concentration is 7%; The weight liquid-solid ratio controlling reaction alkaline pressure of oxygen leaching is 1 ~ 9: 1, and temperature is 150 DEG C, and the treatment time is 1 hour; Adopt lime as reagent reclaiming alkali lye.Reacted material realizes solid-liquid separation, and with pure water cleaning to pH=7.Wherein normal pressure acidleach carries out after the match at ultrasonic wave field; Graphite Powder 99 after process adds sulfuric acid 21% by the weight percent of graphite again, hydrofluoric acid 13% leaches, and the weight liquid-solid ratio controlling normal pressure acidleach is 1 ~ 9:1, and temperature is 35, and the treatment time is 2h.Ultrasonic frequency range during normal pressure acidleach, at 20KHz, obtains highly purified graphite products.Graphite is joined in reactor, is heated with stirring to 75 DEG C, add cerous carbonate in 2% ratio of feed liquid TREO amount, afterwards by TREO 1% amount oxygenant is slowly added, stir, heated and boiled 40 minutes, leave standstill clarification 11 hours, extract the feed liquid of supernatant liquor and band slag respectively, filter.
Embodiment two
Get the graphite 600kg of carbon content > 65%, put into reactor I, first adopt alkaline pressure of oxygen leaching and normal pressure acidleach to process graphite, LiCO used 3concentration is 35%, KOH concentration is 30%, NaHCO 3concentration is 28%; The weight liquid-solid ratio controlling alkaline pressure of oxygen leaching is 1 ~ 9: 1, and temperature is 280 DEG C, and the treatment time is 11 hours; Adopt lime as reagent reclaiming alkali lye.Wherein normal pressure acidleach carries out under microwave field, and the Graphite Powder 99 after process adds sulfuric acid 24% by the weight percent of graphite again, hydrofluoric acid 28% leaches, and the weight liquid-solid ratio controlling normal pressure acidleach is 1 ~ 9:1, and temperature is 85 DEG C, and the treatment time is 90h.Obtain highly purified graphite products.Microwave field range of frequency during control normal pressure acidleach is at 280GHz.Graphite is joined in reactor, is heated with stirring to 85 DEG C, add cerous carbonate in 4% ratio of feed liquid TREO amount, afterwards by TREO 1.5% amount oxygenant is slowly added, stir, heated and boiled 55 minutes, leave standstill clarification 15 hours, extract the feed liquid of supernatant liquor and band slag respectively, filter.

Claims (5)

1. remove impurity SiO for one kind 2and Al 2o 3the method of purification graphite, is characterized in that: the graphite adopting carbon content > 65% is raw material, after purifying, make SIO 2residual quantity≤28MG/L, AL 2o 3residual quantity≤0.2%, purity > 99.99%, step is as follows: the graphite 500-600kg getting carbon content > 65%, puts into reactor I, alkaline pressure of oxygen leaching and normal pressure acidleach is first adopted to process graphite, LiCO used 3concentration is 10% ~ 35%, KOH concentration is 6% ~ 30%, NaHCO 3concentration is 7% ~ 28%; Wherein normal pressure acidleach is at ultrasonic wave field or/and carry out under microwave field, Graphite Powder 99 after process adds sulfuric acid 21%-24% by the weight percent of graphite again, hydrofluoric acid 13%-28% leaches, join in reactor, stirring heating adds cerous carbonate, is slowly added by oxygenant, stirs, heated and boiled, leave standstill clarification, filter, highly purified graphite can be obtained.
2. according to the removal impurity SiO described in claim 1 2and Al 2o 3the method of purification graphite, it is characterized in that the weight liquid-solid ratio of alkaline pressure of oxygen leaching is 1 ~ 9: 1, temperature is 150 ~ 280 DEG C, and the treatment time is 1 ~ 11 hour; Adopt lime as reagent reclaiming alkali lye.
3. according to the removal impurity SiO described in claim 1 2and Al 2o 3the method of purification graphite, is characterized in that wherein normal pressure acidleach is at ultrasonic wave field or/and carry out under microwave field; Graphite Powder 99 after process adds sulfuric acid 21%-24% by the weight percent of graphite again, hydrofluoric acid 13%-28% leaches, and obtains highly purified graphite products,
The weight liquid-solid ratio of normal pressure acidleach is 1 ~ 9:1, and temperature is 35 ~ 85 DEG C, and the treatment time is 2h ~ 90h.
4. according to the removal impurity SiO described in claim 1 2and Al 2o 3the method of purification graphite, ultrasonic frequency range when it is characterized in that normal pressure acidleach is at 20 ~ 70KHz, and microwave field range of frequency is at 280GHz ~ 5GHz.
5. according to the removal impurity SiO described in claim 1 2and Al 2o 3the method of purification graphite, graphite is it is characterized in that to join in reactor, be heated with stirring to 75-85 DEG C, add cerous carbonate in the 2-4% ratio of feed liquid TREO amount, by the amount of the 1-1.5% of TREO, oxygenant is slowly added afterwards, stir, heated and boiled more than 35 minutes, leave standstill clarification more than 10 hours, extract the feed liquid of supernatant liquor and band slag respectively, filter.
CN201310315890.0A 2013-07-25 2013-07-25 Method for removing impurities SiO2 and Al2O3 and purifying graphite Pending CN104340968A (en)

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114524451A (en) * 2021-12-17 2022-05-24 中国北方稀土(集团)高科技股份有限公司 Method for preparing large-particle-size rare earth oxide by one-step microwave at low temperature

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114524451A (en) * 2021-12-17 2022-05-24 中国北方稀土(集团)高科技股份有限公司 Method for preparing large-particle-size rare earth oxide by one-step microwave at low temperature
CN114524451B (en) * 2021-12-17 2024-02-20 中国北方稀土(集团)高科技股份有限公司 Method for preparing large-granularity rare earth oxide by one-step microwave at low temperature

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Application publication date: 20150211