CN101108729A - Method for manufacturing artificial plumbago negative pole material of lithium ion power cell - Google Patents
Method for manufacturing artificial plumbago negative pole material of lithium ion power cell Download PDFInfo
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- CN101108729A CN101108729A CNA2006100148786A CN200610014878A CN101108729A CN 101108729 A CN101108729 A CN 101108729A CN A2006100148786 A CNA2006100148786 A CN A2006100148786A CN 200610014878 A CN200610014878 A CN 200610014878A CN 101108729 A CN101108729 A CN 101108729A
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Abstract
The invention discloses a preparation method of lithium ion power battery artificial graphite cathode materials, which belongs to the lithium ion battery graphite cathode materials technology. The process of the method comprises that the coal pitch or the mixture of the coal pitch and the heavy oil of the secondary oil is added into an autoclave under 380 DEG C. to 450 DEG C. for 7 to 15 hours polymerization; the coal pitch of the same model or the mixture of the coal pitch and the heavy oil of the secondary oil is added into another autoclave under 360 DEG C. to 420 DEG C. for 1 to 6 hours polymerization; the solid-fluid mixtures gained by the two autoclave polymerization are led to the extraction tank according to the volume ratio; the coal tar light fraction, the oil light fraction or toluol is used as the extractant and stirred to be extracted; the extracted mixture is led into a separation device to separate the solid and the fluid; the particulate matters are heated, dried and classified to produce the artificial graphite ball with average grain size of 6Mum to 13Mum and the graphitization degree d002 is between 0.335nm to 0.337nm. The invention is characterized in by technological process, high product yield, low manufacture cost and process with better environment protection.
Description
Technical field
The present invention relates to a kind of preparation method of artificial plumbago negative pole material of lithium ion power cell, belong to silicon/carbon/graphite in lithium ion batteries negative material technology.
Background technology
The research of the lithium cell of China continues nearly 20 years, and along with to the improvement of current material and battery design technology and the appearance of novel material, the range of application of lithium ion battery is constantly expanded.Comprise civilian information industry, energy traffic, and military submarine, unmanned aerial vehicle, satellite etc.The lithium-ion electric pool technology has not been a simple industrial technology, its concern development of information industry, and one of basic technology of new forms of energy industry development especially, and become one of modern and following military equipment indispensable important " grain ".
At present China has become the second-biggest-in-the-world lithium ion battery producing country that is only second to Japan, at lithium electricity miniaturization technology relatively after the maturation, develops large-scale lithium ion battery and relevant novel material becomes active demand.And the bottleneck one that influences power cell development at present is cost, the 2nd, and battery performance (as: high-rate discharge ability, rapid charge time, long cycle life and for the adaptability of severe environment etc.).
Wherein the selection of cell negative electrode material directly influences the performance of lithium ion battery.Though natural graphite has higher specific storage in the raw material of wood-charcoal material, be easy to react with electrolytic solution, make solvent molecule embed altogether and cause peeling off of graphite linings, the reversible capacity of battery reduces, and the cycle performance of lithium ion battery descends.The way that solves is to carry out modification to handle on the natural graphite surface, and wherein the way of Bao Fuing is difficult to once coat complete, and the secondary coating has then increased cost and difficulty.Other materials charcoal fiber and carbon nanotube manufacturing process be wayward to exist very big difficulty in practicality.Synthetic graphite MCMB perfect structure embedding lithium superior performance comparatively speaking, the specific storage height has extended cycle life, and the pole piece process industrial art performance is good, obtains in the industry extensively certainly and uses.High-rate discharge ability research MCMB is had higher relatively electronic conductivity and lithium velocity of diffusion, and discover that the small-particle carbon microspheres has more superior high rate during charging-discharging than macrobead material.Because the electric current that small-particle can make unit surface load reduces, help reducing overpotential, the edge of carbon crystallite can provide more migrating channels for lithium ion, and the path of lithium ion migration is shortened, and diffusion impedance reduces.Carbon microspheres has good structure properties simultaneously, has guaranteed the cycle life of battery, is a kind of developable power lithium-ion battery artificial plumbago negative pole material.At present in the thermal polycondensation process production MCMB, productive rate is less than 23% between 14～25 μ m the time for the copolycondensation preparation method production median size of patent ZL00133301.1 MCMB, and productive rate will be lower between 6～13 μ m the time to produce particle diameter d (0.5) according to processing requirement.To effectively improve the productive rate of product if employing is mitogenetic with washing separation of polymeric technology, reduce product cost, satisfy the demand in market.
Summary of the invention
The preparation method who the purpose of this invention is to provide a kind of artificial plumbago negative pole material of lithium ion power cell, this method has the advantages that process is simple, product yield is high and production cost is low.
The present invention is realized by following technical proposals, a kind of preparation method of artificial plumbago negative pole material of lithium ion power cell, and described artificial plumbago negative pole material is meant that median size is 6～13 μ m granular graphites, is characterized in that comprising following process:
(1) mixture (volume ratio 4: 1) with coal-tar pitch or coal-tar pitch and secondary petroleum heavy oil adds in the reactor, at 380～450 ℃, and thermopolymerization 7～15 hours.
(2) employing adds in another reactor with the coal-tar pitch of the mutually same model of step (1) or the mixture (volume ratio 4: 1) of coal-tar pitch and secondary petroleum heavy oil, at 360～420 ℃, and thermopolymerization 1～6h.
(3) solidliquid mixture that step (1) and step (2) polymerization are obtained (7～3) by volume: (3～7) import in the extraction tank, are that extraction agent extracts it under whipped state with coal tar light ends, oil light ends or toluene.Temperature is controlled to be lower than under 20 ℃ of the solvent boiling points and extracts.
(4) will carry out solid-liquid separation in step (3) the extraction mixture lead-in separation device.
(5) the particulate matter heating, drying that obtains of step (4), then by classification, extracting median size is 6～13 μ m particulate matter, this particulate matter is carried out graphitization processing under 2800 ℃ temperature, obtaining median size is the rostone tampon of 6～13 μ m, graphite layers apart from d002 between 0.335～0.337nm.
Characteristics of the present invention are, the separating technology that adopts is mitogenetic with washing partition method, i.e. thermal polycondensation reaction under two kinds of different conditions, in colloidal dispersion separately, generate the product of different-grain diameter, common extracting and separating in proportion is mixed each still solidliquid mixture, solved the loss in pure small particle size extracting and separating and the cleaning process, and washing lotion to be difficult to infiltrate through filter cake be the method that filter cake is difficult to soak into cleaning.This technology has improved the purity of material, has reduced the usage quantity of solvent, has simplified technological process, has improved product yield, has reduced manufacturing cost, more environmental protection.
Embodiment
Embodiment 1 injects polymeric kettle No. 1 with medium temperature coal pitch 400mL and ethylene bottom oil 100mL, slowly heating under agitation condition.Temperature is controlled at 415 ℃ of insulation 10h.The medium temperature coal pitch 400mL and the ethylene bottom oil 100mL of same model are injected polymeric kettle No. 2, slowly heating under agitation condition.Temperature is controlled at 400 ℃ of insulation 3h.When the two still materials that the while polymerization is finished are cooled to 300 ℃, No. 1 product and No. 2 products are imported in the same extraction tank, add washing oil and under agitation extract 3h, 115 ℃ of extraction temperature, then by tripping device with solid-liquid separation.Isolated solid cleans back 120 ℃ of dry 3h with toluene, and dried solid is classified, and extracting median size is the product of 6～13 μ m, obtains rostone tampon finished product through 2800 ℃ of graphitization processing, and graphite layers is apart from d
002Between 0.335～0.337nm.
Embodiment 2 injects polymeric kettle No. 1 with medium temperature coal pitch 500mL, slowly heating under agitation condition.Temperature is controlled at 415 ℃ of insulation 10h.The medium temperature coal pitch 500mL of same model is injected polymeric kettle No. 2, slowly heating under agitation condition.Temperature is controlled at 400 ℃ of insulation 3h.When the two still materials that the while polymerization is finished are cooled to 300 ℃, No. 1 product and No. 2 products are imported with in the extraction tank together, add washing oil and under agitation extract 3h, 120 ℃ of extraction temperature, then by tripping device with solid-liquid separation.Isolated solid with toluene clean back 120 ℃ in dry 3h, dried solid is classified, and extracting median size is the product of 6～13 μ m, obtains rostone tampon finished product through 2800 ℃ of graphitization processing, graphite layers is apart from d
002Between 0.335～0.337nm.
Embodiment 3 injects No. 1 polymeric kettle with medium temperature coal pitch 400mL and ethylene bottom oil 100mL, slowly heating under agitation condition.Temperature is controlled at 400 ℃ of insulation 10h.The medium temperature coal pitch 600mL and the ethylene bottom oil 150mL of same model are injected another polymeric kettle No. 2, slowly heating under agitation condition.Temperature is controlled at 380 ℃ of insulation 5h.When the two still materials that the while polymerization is finished are cooled to 300 ℃, No. 1 product and No. 2 products are imported add washing oil in the extraction tank and under agitation extract 3h, 115 ℃ of extraction temperature, then by tripping device with solid-liquid separation.Isolated solid cleans back 120 ℃ of dry 3h with toluene, and dried solid is classified, and extracting median size is the product of 6～13 μ m, obtains novel artificial graphite pebbles finished product through 2800 ℃ of graphitization processing, requires graphite layers apart from d
002Between 0.335～0.337nm.
Embodiment 4 injects No. 1 polymeric kettle with medium temperature coal pitch 500mL, slowly heating under agitation condition.Temperature is controlled at 400 ℃ of insulation 10h.The medium temperature coal pitch 750mL of same model is injected another polymeric kettle No. 2, slowly heating under agitation condition.Temperature is controlled at 380 ℃ of insulation 5h.When the two still materials that the while polymerization is finished are cooled to 300 ℃, No. 1 product and No. 2 products are imported add washing oil in the extraction tank and under agitation extract 3h, 200 ℃ of extraction temperature, then by tripping device with solid-liquid separation.Isolated solid cleans back 120 ℃ of dry 3h with toluene, and dried solid is classified, and extracting median size is the product of 6～13 μ m, obtains rostone tampon finished product through 2800 ℃ of graphitization processing, and graphite layers is apart from d
002Between 0.335～0.337nm.
Embodiment 5 injects No. 1 polymeric kettle with medium temperature coal pitch 600mL and ethylene bottom oil 150mL, slowly heating under agitation condition.Temperature is controlled at 415 ℃ of insulation 10h.The medium temperature coal pitch 400mL and the ethylene bottom oil 100mL of same model are injected another polymeric kettle No. 2, slowly heating under agitation condition.Temperature is controlled at 410 ℃ of insulation 2h.When the two still materials that the while polymerization is finished are cooled to 300 ℃, will No. 1 product and No. 2 products import and add washing oil extraction 3h in the extraction tanks, 115 ℃ of extraction temperature, then by tripping device with solid-liquid separation.Isolated solid cleans back 120 ℃ of dry 3h with toluene, and dried solid is classified, and extracting median size is the product of 6～13 μ m, obtains rostone tampon finished product through 2800 ℃ of graphitization processing, and graphite layers is apart from d
002Between 0.335～0.337nm.
Embodiment 6 injects No. 1 polymeric kettle with medium temperature coal pitch 750mL, slowly heating under agitation condition.Temperature is controlled at 415 ℃ of insulation 10h.The medium temperature coal pitch 500mL of same model is injected another polymeric kettle No. 2, slowly heating under agitation condition.Temperature is controlled at 410 ℃ of insulation 2h.When the two still materials that the while polymerization is finished are cooled to 300 ℃, will No. 1 product and No. 2 products import and add washing oil extraction 3h in the extraction tanks, 200 ℃ of extraction temperature, then by tripping device with solid-liquid separation.Isolated solid cleans back 120 ℃ of dry 3h with toluene, and dried solid is classified, and extracting median size is the product of 6～13 μ m, obtains rostone tampon finished product through 2800 ℃ of graphitization processing, and graphite layers is apart from d
002Between 0.335～0.337nm.
Comparative example 1 injects polymeric kettle with medium temperature coal pitch 500mL, slowly heating under agitation condition.Temperature is controlled at 400 ℃ of insulation 3h.Heat tracing finishes, and blowing is gone in the extraction tank when naturally cooling to 300 ℃, adds washing oil and stirs, and is incubated 200 ℃, extraction 3h.With solid-liquid separation, solid cleans behind back 120 ℃ of dry 3h classified with toluene by tripping device, and extracting median size is the product of 6～13 μ m, obtains finished product rostone tampon through 2800 ℃ of graphitization processing, requires graphite layers apart from d
002Between 0.335～0.337nm.
The physicals test median size of the rostone tampon that makes with the present invention is measured by Britain Malvern-Mastersizer2000 laser particle size analyzer, specific surface area is measured by U.S.'s health tower Qusntachrome-NOVA 1000e specific surface and porosity tester, tap density goes out the FZS4-4 type tap density determinator of Iron and Steel Research Geueral Inst to be measured, and crystal pitch is measured by Japan's motor D of science/Max-2005 X-ray diffractometer.
Yield calculates:
m
0--preparation process raw material add-on/Kg
m
1--amount of solid/Kg that drying finishes
Test result sees Table 1.
Table 1 physical testing result
| Example | Mean particle size μ m | Specific surface area m 2/g | Tap density g/cm 3 | Yield % | The solvent consumption ton |
| Embodiment 1 | 8.029 | 1.51 | 1.18 | 24.7 | 13.8 |
| Embodiment 2 | 8.252 | 1.50 | 1.19 | 20.5 | 13.9 |
| Embodiment 3 | 10.604 | 1.48 | 1.24 | 23.4 | 15.4 |
| Embodiment 4 | 10.315 | 1.46 | 1.23 | 18.7 | 15.6 |
| Embodiment 5 | 6.672 | 1.56 | 1.16 | 23.9 | 13.4 |
| Embodiment 6 | 6.894 | 1.57 | 1.17 | 19.3 | 13.3 |
| Comparative example 1 | 10.624 | 1.49 | 1.23 | 17.2 | 17.4 |
Annotate: solvent consumption with 1 ton of greying of every production before the required quantity of solvent of solid material.
Adjust the processing parameter of reaction process according to test result, produce the rostone tampon of peculiar size, adopt and mitogeneticly make the graphite pebbles production technology with washing the separation of polymeric legal person, produce the power-type lithium ion battery negative material of high-performance low price, improved the productive rate of rostone tampon, different-grain diameter has reduced the difficulty of cleaning process in conjunction with cleaning, reduced the usage quantity of organic solvent, reduced the recovery of waste, become pollution-free, the material of environmental protection.
By to making the technology adjustment of artificial graphite pebbles, the mean particle size that changes condition may command products such as polymerization temperature, polymerization time between 3～15 μ m, stable physical property after tested.
Product and oiliness binding agent PVDF (polyvinylidene difluoride (PVDF)), conductive agent that electrochemical property test is made the foregoing description and comparative example respectively mix with 90: 4: 6 mass ratio, binding agent PVDF should be dissolved in earlier among the NMP (N-Methyl pyrrolidone), the cathode size that mixes is coated on the Copper Foil uniformly, and carries out drying, cut and make cathode pole piece.Positive electrode material adopts LiCoO
2Be coated on the aluminium foil as anode pole piece, electrolytic solution adopts 1.2MLiPF
6The solution of PC/EC/EMC/VC.Carry out charge-discharge test after above-mentioned materials is assembled into rectangular cell, the equipment that test is used is tested as Shenzhen Xin Wei BTS of Electronics Co., Ltd. type battery test system.Test index comprises that loading capacity, test multiplying power discharging property adopt 0.2C, 1C, 2C, 5C, 10C, 15C, 20C discharge, sparking voltage 4.2～2.75V first.
Test result is listed in table 2.
Table 2. electrochemical property test result
| Discharge-rate | Test index | Embodiment 1 | Embodiment 2 | Embodiment 3 | Embodiment 4 | Embodiment 5 | Embodiment 6 |
| 0.2C | Specific discharge capacity mAh/g | 330 | 329 | 321 | 323 | 327 | 325 |
| 1C | 1C/0.2C％ | 99.8 | 99.8 | 99.4 | 99.5 | 99.7 | 99.6 |
| 2C | 2C/0.2C％ | 99.6 | 99.7 | 99.2 | 99.2 | 99.6 | 99.6 |
| 5C | 5C/0.2C％ | 98.5 | 99.5 | 98.0 | 97.9 | 98.3 | 98.4 |
| 10C | 10C/0.2C％ | 94.2 | 94.1 | 92.9 | 92.8 | 93.7 | 93.5 |
| 15C | 15C/0.2C％ | 92.1 | 92.3 | 91.3 | 91.1 | 91.9 | 91.7 |
| 20C | 20C/0.2C％ | 90.6 | 90.5 | 90.0 | 89.9 | 90.5 | 90.3 |
By the rostone tampon is carried out electric performance test, shown good discharge performance for the heavy-current discharge aspect, illustrate that product having unique advantage aspect the big multiplying power discharging, can satisfy the requirement of market to the power type lithium secondary battery cathode material.
Claims (1)
1. the preparation method of an artificial plumbago negative pole material of lithium ion power cell, described artificial plumbago negative pole material is meant that median size is 6～13 μ m granular graphites, is characterized in that comprising following process:
(1) with coal-tar pitch or coal-tar pitch and secondary petroleum heavy oil be 4: 1 mixture by volume, add in the reactor, under 380～450 ℃, thermopolymerization 7～15 hours;
(2) adopt with in the coal-tar pitch of the mutually same model of step (1) or coal-tar pitch and secondary petroleum heavy oil are 4: 1 mixture adding reactor by volume, at 360～420 ℃, thermopolymerization 1～6h;
(3) with step (1) and step (2) solidliquid mixture that obtains of polymerization (7～3) by volume respectively: (3～7) import in the extraction tank, with coal tar light ends, oil light ends or toluene is that extraction agent extracts under whipped state, and extraction temperature is controlled at and is lower than 20 ℃ of solvent boiling points;
(4) carry out solid-liquid separation in the extract lead-in separation device that obtains with step (3);
(5) the particulate matter heating, drying that step (4) is obtained, by classification, extracting median size is 6～13 μ m particulate matter then, and this particulate matter is carried out graphitization processing under 2800 ℃ temperature, obtaining median size is the rostone tampon of 6～13 μ m, and graphite layers is apart from d
002Between 0.335～0.337nm.
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Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101570330A (en) * | 2009-03-07 | 2009-11-04 | 垦利三合新材料科技有限责任公司 | Method for preparing modified natural graphite nodules |
| CN101880042A (en) * | 2010-06-02 | 2010-11-10 | 天津大学 | Artificial graphite microspheres for preparing cathode of lithium ion battery and preparation method thereof |
| CN102104141A (en) * | 2010-12-25 | 2011-06-22 | 雷铁军 | Method for preparing graphite anode material of membrane-structural lithium ion battery by hot coating method |
| CN107324327A (en) * | 2017-07-11 | 2017-11-07 | 陕西科技大学 | A kind of method and purposes using coal as the direct synthetic graphite material of raw material |
| CN108483437A (en) * | 2018-03-19 | 2018-09-04 | 天津锦美碳材科技发展有限公司 | It is a kind of using ethylene coke as lithium cell carbon cathode material of raw material and preparation method thereof |
| CN109671938A (en) * | 2018-12-21 | 2019-04-23 | 赣州市瑞富特科技有限公司 | Compound coating type graphite cathode material with hamburger structure and preparation method thereof |
| CN109713237A (en) * | 2017-10-26 | 2019-05-03 | 宁德时代新能源科技股份有限公司 | Lithium ion secondary battery |
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2006
- 2006-07-20 CN CNB2006100148786A patent/CN100554150C/en active Active
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101570330A (en) * | 2009-03-07 | 2009-11-04 | 垦利三合新材料科技有限责任公司 | Method for preparing modified natural graphite nodules |
| CN101880042A (en) * | 2010-06-02 | 2010-11-10 | 天津大学 | Artificial graphite microspheres for preparing cathode of lithium ion battery and preparation method thereof |
| CN102104141A (en) * | 2010-12-25 | 2011-06-22 | 雷铁军 | Method for preparing graphite anode material of membrane-structural lithium ion battery by hot coating method |
| CN107324327A (en) * | 2017-07-11 | 2017-11-07 | 陕西科技大学 | A kind of method and purposes using coal as the direct synthetic graphite material of raw material |
| CN107324327B (en) * | 2017-07-11 | 2019-05-24 | 陕西科技大学 | It is a kind of using coal as the method and purposes of the direct synthetic graphite material of raw material |
| CN109713237A (en) * | 2017-10-26 | 2019-05-03 | 宁德时代新能源科技股份有限公司 | Lithium ion secondary battery |
| CN108483437A (en) * | 2018-03-19 | 2018-09-04 | 天津锦美碳材科技发展有限公司 | It is a kind of using ethylene coke as lithium cell carbon cathode material of raw material and preparation method thereof |
| CN108483437B (en) * | 2018-03-19 | 2021-07-09 | 安徽锦美碳材科技发展有限公司 | Lithium battery carbon negative electrode material taking ethylene coke as raw material and preparation method thereof |
| CN109671938A (en) * | 2018-12-21 | 2019-04-23 | 赣州市瑞富特科技有限公司 | Compound coating type graphite cathode material with hamburger structure and preparation method thereof |
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