CN110272045B - High-activity coke and preparation method thereof - Google Patents

High-activity coke and preparation method thereof Download PDF

Info

Publication number
CN110272045B
CN110272045B CN201910658020.0A CN201910658020A CN110272045B CN 110272045 B CN110272045 B CN 110272045B CN 201910658020 A CN201910658020 A CN 201910658020A CN 110272045 B CN110272045 B CN 110272045B
Authority
CN
China
Prior art keywords
coal
coking
coke
blended coal
blended
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.)
Active
Application number
CN201910658020.0A
Other languages
Chinese (zh)
Other versions
CN110272045A (en
Inventor
杨立新
李轶
高云祥
刘锋
王映荣
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.)
Wugang Group Kunming Iron and Steel Co Ltd
Original Assignee
Wugang Group Kunming Iron and Steel 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 Wugang Group Kunming Iron and Steel Co Ltd filed Critical Wugang Group Kunming Iron and Steel Co Ltd
Priority to CN201910658020.0A priority Critical patent/CN110272045B/en
Publication of CN110272045A publication Critical patent/CN110272045A/en
Application granted granted Critical
Publication of CN110272045B publication Critical patent/CN110272045B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B32/00Carbon; Compounds thereof
    • C01B32/30Active carbon
    • C01B32/312Preparation
    • C01B32/318Preparation characterised by the starting materials
    • C01B32/33Preparation characterised by the starting materials from distillation residues of coal or petroleum; from petroleum acid sludge
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/10Process efficiency

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Materials Engineering (AREA)
  • Inorganic Chemistry (AREA)
  • Coke Industry (AREA)

Abstract

The invention discloses high-activity coke and a preparation method thereof. The high-activity coke is prepared by taking blended coal and refined iron powder as raw materials and performing pretreatment and coking steps, wherein the blended coal is 1/3 coking coal and coking coal mixed coal. The method comprises the steps of pretreatment and coking, and specifically comprises the following steps: 1/3, uniformly mixing the coking coal and the coking coal according to a formula ratio to blend coal, and adding water to adjust the water content of the blend coal to 9-12%; adding the iron concentrate powder with the formula ratio into the blended coal, and uniformly mixing to obtain a material a; and (4) coking the material a to obtain the target high-activity coke. The high-activity coke has high reactivity and stable reactive strength, can greatly reduce the temperature of a heat balance zone of the blast furnace, reduce the coke ratio of the blast furnace and realize energy conservation and emission reduction of the blast furnace.

Description

High-activity coke and preparation method thereof
Technical Field
The invention belongs to the technical field of iron making, and particularly relates to high-activity coke and a preparation method thereof.
Background
With the improvement of national requirements on energy conservation and environmental protection in blast furnace iron making, the iron making industry generally considers that the blast furnace urgently needs coke with moderate heat strength and strong activation performance so as to improve the development of indirect reduction degree of the blast furnace, promote the reduction of coke ratio, coal ratio and fuel ratio of the blast furnace, and achieve the purposes of energy conservation and emission reduction in the iron making process. Therefore, it is very necessary to develop a highly active coke.
Disclosure of Invention
A first object of the present invention is to provide a highly active coke; the second purpose is to provide the preparation method of the high-activity coke.
The first purpose of the invention is realized by that the high activity coke is prepared by using blended coal and refined iron powder as raw materials through pretreatment and coking steps, and the blended coal is 1/3 coking coal and coking coal mixed coal.
The second purpose of the invention is realized by the following steps, including pretreatment and coking steps:
A. pretreatment:
1) preparing blended coal: 1/3, uniformly mixing the coking coal and the coking coal according to a formula ratio to blend coal, and adding water to adjust the water content of the blend coal to 9-12%;
2) adding the iron concentrate powder with the formula ratio into the blended coal, and uniformly mixing to obtain a material a;
B. coking: and (4) coking the material a to obtain the target high-activity coke.
The high-activity coke has high reactivity and stable reactive strength, can greatly reduce the temperature of a heat balance zone of the blast furnace, reduce the coke ratio of the blast furnace and realize energy conservation and emission reduction of the blast furnace.
Detailed Description
The present invention is further illustrated by the following examples, which are not intended to be limiting in any way, and any modifications or alterations based on the teachings of the present invention are intended to fall within the scope of the present invention.
The high-activity coke is prepared by taking blended coal and refined iron powder as raw materials and performing pretreatment and coking steps, wherein the blended coal is 1/3 coking coal and coking coal mixed coal.
The reactivity of the high-activity coke is more than 35%, and the strength after reaction is more than 55%.
The 1/3 coking coal and coking coal are in a mass ratio of (4-5): (5-6).
The water content of the blended coal is 9-12%.
The addition amount of the fine iron powder is 0.4-0.6% of the mass percentage of the blended coal.
The iron content of the fine iron powder is 50-60%.
The iron content of the fine iron powder is 54 percent.
The preparation method of the high-activity coke comprises the steps of pretreatment and coking, and specifically comprises the following steps:
A. pretreatment:
1) preparing blended coal: blending 1/3 coking coal and coking coal into blended coal according to a formula ratio, and adding water to adjust the water content of the blended coal to 9-12%;
2) adding the iron concentrate powder with the formula ratio into the blended coal, and uniformly mixing to obtain a material a;
B. and (3) coking: and (4) coking the material a to obtain the target high-activity coke.
And in the coking step, the material a is placed in an environment with the temperature of 1200-1300 ℃ at the wall machine side of the coke oven and the temperature of 1300-1350 ℃ at the coke side for coking for 15-25 h.
The coking is to coke the material a for 19-21 hours in an environment with the wall temperature of a coke oven of 1220-1290 ℃ and the coke side temperature of 1310-1340 ℃.
The invention is further illustrated by the following specific examples:
example 1
Firstly, adding water into blended coal (the blending ratio is 1/3 coking coal 45 percent and 55 percent) and uniformly mixing, wherein the water content of the blended coal is 10.5 percent.
Secondly, mixing the blended coal and iron concentrate powder containing 54.00% of iron and 0.5% of the total amount of the blended coal uniformly.
Thirdly, controlling the temperature of the wall of the coke oven to 1230 ℃ at the machine side and 1310 ℃ at the coke side, and carrying out normal coking operation for 21 h. The coke reactivity was 35.50% and the strength after reaction was 61.32%.
Example 2
Firstly, adding water into blended coal (the blending ratio is 1/3 coking coal 40% and 60%) and uniformly mixing, wherein the water content of the blended coal is 9.8%.
Secondly, mixing the blended coal and iron concentrate powder containing iron and 54 percent of 3.0 percent of the total amount of the blended coal uniformly.
Thirdly, controlling the temperature of the wall of the coke oven to be 1250 ℃ at the machine side and 1330 ℃ at the coke side, and carrying out normal coking operation within 20 h. The coke reactivity was 40.50% and the post-reaction strength was 58.37%.
Example 3
Firstly, adding water into blended coal (the blending ratio is 1/3 coking coal 50 percent and 50 percent of coking coal) and uniformly mixing, wherein the water content of the blended coal is 11.6 percent.
Secondly, mixing the blended coal and iron concentrate powder containing iron and 54 percent, which is 1.2 percent of the total amount of the blended coal.
Thirdly, the temperature of the wall of the coke oven is controlled to be 1260 ℃ on the machine side and 1340 ℃ on the coke side, and the coking time is controlled to be 19.5 hours for normal coking operation. The coke reactivity was 37.00% and the post-reaction strength was 60.87%.
Example 4
Firstly, adding water into blended coal (the blending ratio is 1/3 coking coal 45 percent and 55 percent) and uniformly mixing, wherein the water content of the blended coal is 10.1 percent.
Secondly, mixing the blended coal and iron concentrate powder containing iron and 54 percent, wherein the iron concentrate powder is 2.2 percent of the total amount of the blended coal.
Thirdly, controlling the temperature of the wall of the coke oven to be 1280 ℃, and carrying out normal coking operation within 19 hours of coking time. The coke reactivity was 42.50% and the post-reaction strength was 57.74%.

Claims (4)

1. The high-activity coke is characterized by being prepared by taking blended coal and refined iron powder as raw materials and performing pretreatment and coking steps, wherein the blended coal is 1/3 coking coal and mixed coal with a coking coal mass ratio of (4-5) to (5-6), the water content of the blended coal is 9-12%, and the addition amount of the refined iron powder is 0.5%, 1.2%, 2.2% or 3.0% of the mass percent of the blended coal; the preparation method of the high-activity coke comprises the steps of pretreatment and coking, and specifically comprises the following steps:
A. pretreatment:
1) preparing blended coal: blending 1/3 coking coal and coking coal into blended coal according to a formula ratio, and adding water to adjust the water content of the blended coal to 9-12%;
2) adding the iron concentrate powder with the formula ratio into the blended coal, and uniformly mixing to obtain a material a;
B. and (3) coking: and (2) coking the material a, namely, putting the material a in an environment of 1200-1300 ℃ on the wall side of a coke oven and 1300-1350 ℃ on the coke side for coking for 15-25 h to obtain the target high-activity coke, wherein the reactivity of the high-activity coke is more than 35%, and the strength after reaction is more than 55%.
2. The highly active coke according to claim 1, wherein the iron content of the fine iron powder is 50 to 60%.
3. The highly active coke according to claim 1, wherein the iron content of the fine iron powder is 54%.
4. The high activity coke of claim 1, wherein the material a is placed in an environment with a coke oven wall temperature of 1220-1290 ℃ and a coke side temperature of 1310-1340 ℃ for coking for 19-21 h.
CN201910658020.0A 2019-07-20 2019-07-20 High-activity coke and preparation method thereof Active CN110272045B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201910658020.0A CN110272045B (en) 2019-07-20 2019-07-20 High-activity coke and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201910658020.0A CN110272045B (en) 2019-07-20 2019-07-20 High-activity coke and preparation method thereof

Publications (2)

Publication Number Publication Date
CN110272045A CN110272045A (en) 2019-09-24
CN110272045B true CN110272045B (en) 2022-07-12

Family

ID=67964858

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201910658020.0A Active CN110272045B (en) 2019-07-20 2019-07-20 High-activity coke and preparation method thereof

Country Status (1)

Country Link
CN (1) CN110272045B (en)

Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2001348576A (en) * 2000-04-04 2001-12-18 Nippon Steel Corp Method for producing highly reactive coke for blast furnace
JP2004300175A (en) * 2003-03-28 2004-10-28 Nippon Steel Corp Manufacturing method of highly reactive molded coke for blast furnace
CN102453490A (en) * 2010-10-22 2012-05-16 宝山钢铁股份有限公司 Coal blending method for preparing high-activity high-strength coke
CN102719264A (en) * 2011-03-29 2012-10-10 鞍钢股份有限公司 High-reactivity coke and production method thereof
CN102851049A (en) * 2011-06-27 2013-01-02 宝山钢铁股份有限公司 Coal blending method for high-reactivity coke for blast furnace
CN103468287A (en) * 2013-09-22 2013-12-25 重庆大学 Preparation method of high strength-hyper reactivity iron containing coke
KR101657402B1 (en) * 2015-03-26 2016-09-13 현대제철 주식회사 High reactivity and high strength coke for blast furnace and method of producing the same
CN107709523A (en) * 2015-06-24 2018-02-16 杰富意钢铁株式会社 The manufacture method of iron coke
CN108219807A (en) * 2016-12-13 2018-06-29 鞍钢股份有限公司 Preparation method of biomass iron coke for blast furnace
CN108913181A (en) * 2018-07-19 2018-11-30 武钢集团昆明钢铁股份有限公司 A kind of high calcium is burnt and its production method

Patent Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2001348576A (en) * 2000-04-04 2001-12-18 Nippon Steel Corp Method for producing highly reactive coke for blast furnace
JP2004300175A (en) * 2003-03-28 2004-10-28 Nippon Steel Corp Manufacturing method of highly reactive molded coke for blast furnace
CN102453490A (en) * 2010-10-22 2012-05-16 宝山钢铁股份有限公司 Coal blending method for preparing high-activity high-strength coke
CN102719264A (en) * 2011-03-29 2012-10-10 鞍钢股份有限公司 High-reactivity coke and production method thereof
CN102851049A (en) * 2011-06-27 2013-01-02 宝山钢铁股份有限公司 Coal blending method for high-reactivity coke for blast furnace
CN103468287A (en) * 2013-09-22 2013-12-25 重庆大学 Preparation method of high strength-hyper reactivity iron containing coke
KR101657402B1 (en) * 2015-03-26 2016-09-13 현대제철 주식회사 High reactivity and high strength coke for blast furnace and method of producing the same
CN107709523A (en) * 2015-06-24 2018-02-16 杰富意钢铁株式会社 The manufacture method of iron coke
CN108219807A (en) * 2016-12-13 2018-06-29 鞍钢股份有限公司 Preparation method of biomass iron coke for blast furnace
CN108913181A (en) * 2018-07-19 2018-11-30 武钢集团昆明钢铁股份有限公司 A kind of high calcium is burnt and its production method

Also Published As

Publication number Publication date
CN110272045A (en) 2019-09-24

Similar Documents

Publication Publication Date Title
CN101705333B (en) Reduction and utilization method of dedusting ash of stainless steel
CN102399978B (en) Manufacture method of iron ore MgO pellet ore
CN102644015A (en) Production method for vanadium nitride ferroalloy
CN101613798B (en) Puddling additive and predation method thereof
CN110330993B (en) Dual-functional binder-based blended coal coking method
CN106010707A (en) Forming method of semicoke powder and quicklime powder
CN105755195B (en) A method of molten steel is directly prepared from high-silicon iron ore
CN101177731B (en) Method for preparing sintered ore
CN110272045B (en) High-activity coke and preparation method thereof
CN107142120B (en) High-reactivity coke and preparation method thereof
CN103627897B (en) Rich iron cooled agglomerated pellet and manufacturing process thereof and purposes
CN113088310B (en) Tamping coal blending coking method, product thereof and blended coal for coking
CN111470788B (en) Mixed injection fuel for Meerz kiln and injection method thereof
CN102424586A (en) Preparation method of SiC fireproof raw material powder
CN102041379A (en) Utilization method of acid remelted iron powder
KR20030013056A (en) Method of Briquettes having superior strength
CN103571489A (en) Method for synthesizing small-granularity narrow-distribution green fluorescent precursor
CN103773549B (en) Coke increases block agent and preparation technology thereof
CN103710531B (en) A kind of method improving vanadium titanium sinter mixture temperature
CN113462901A (en) Method for smelting titanium-containing slag
CN112279651A (en) Ramming material and preparation method thereof
CN114507553A (en) Mixed fuel with high coal-coke replacement ratio for blast furnace injection and preparation method thereof
CN101343688B (en) Pelletization method for vanadium titanium magnet ore concentrate mixing with additive rough rice shell
CN111593168A (en) Slag iron separation accelerant and preparation method and use method thereof
KR100518326B1 (en) Method of manufacturing briquettes having superior strength

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
GR01 Patent grant
GR01 Patent grant