CN104630566B - Ferro-nickel alloy and preparation method thereof - Google Patents

Ferro-nickel alloy and preparation method thereof Download PDF

Info

Publication number
CN104630566B
CN104630566B CN201510064491.0A CN201510064491A CN104630566B CN 104630566 B CN104630566 B CN 104630566B CN 201510064491 A CN201510064491 A CN 201510064491A CN 104630566 B CN104630566 B CN 104630566B
Authority
CN
China
Prior art keywords
dilval
refining
ferro
preparation
nickel alloy
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.)
Expired - Fee Related
Application number
CN201510064491.0A
Other languages
Chinese (zh)
Other versions
CN104630566A (en
Inventor
梅百荣
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.)
Hunan Zhongwei Holding Group Co., Ltd.
Original Assignee
Tongling Hundred Flourish Type Material Foundry Goods 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 Tongling Hundred Flourish Type Material Foundry Goods Co Ltd filed Critical Tongling Hundred Flourish Type Material Foundry Goods Co Ltd
Priority to CN201510064491.0A priority Critical patent/CN104630566B/en
Publication of CN104630566A publication Critical patent/CN104630566A/en
Application granted granted Critical
Publication of CN104630566B publication Critical patent/CN104630566B/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Landscapes

  • Manufacture And Refinement Of Metals (AREA)

Abstract

The invention discloses a ferro-nickel alloy and a preparation method thereof. The ferro-nickel alloy comprises the following components in percentage by weight: 38-50% of Ni, 0.8-1.5% of C, 0.5-1.5% of Si, 0.03-0.10% of P, 0.01-0.05% of S, 1-2.5% of Cr, 0.5-1.0% of Co and the balance of Fe. The preparation method comprises the steps of (1) mixing and pelleting; (2) reducing; (3) smelting, namely firstly carrying out solid phase sintering on the a metalized pellet at the temperature of 1000-1350 DEG C for 4-6 days, further heating to 1500-1750 DEG C, and smelting for 1-3 hours to obtain crude ferro-nickel alloy; and (4) refining, namely refining the crude ferro-nickel alloy, adding basic oxide accounting for 2.5-3.5% of the weight of the crude ferro-nickel alloy while refining to obtain refined molten ferro-nickel, and then, pouring to obtain a refined ferro-nickel alloy product, wherein the refining temperature is 1500-1700 DEG C, the refining period is 30-50 minutes, and the oxygen blowing quantity is 100-200Nm<3>/t. The ferro-nickel alloy and the preparation method thereof have the advantages that the prepared ferro-nickel alloy is high in density and purity and good in strength, toughness and wear resistance; and the preparation method is simple, low in production cost and remarkable in energy-saving and emission-reduction effects.

Description

A kind of dilval and preparation method thereof
Technical field
The present invention relates to technical field of iron alloy, more particularly, to a kind of dilval and preparation method thereof.
Background technology
Ferroalloy, the ferroalloy of broad sense refers to add as deoxidier, element additive etc. during steel-making makes steel have in molten iron Certain characteristic standby or a kind of product reaching certain requirement, iron and the intermediate alloy of one or more elements composition, are mainly used in Smelting iron and steel.Nickel can be melt into dilval with iron, form the light-alloy of high intensity, have a wide range of applications in every respect.At present The conventional method producing dilval the domestic nickel ore from nickeliferous 1.5-2.5% is mainly sintered using nickel minerals, Make solvent with lime, make reducing agent with coke and carry out the prepared dilval product of selective reduction in ore-smelting electric furnace, for producing Stainless steel uses, and its traditional processing technology is more complicated, and low production efficiency, sintering circuit coke consumption are high, and lime was producing Easy efflorescence in journey, coke price is expensive, and costly, pollution is big.
Content of the invention
The purpose of the present invention is to overcome the deficiencies in the prior art, provides a kind of dilval and preparation method thereof, preparation Dilval density and purity are high, and intensity, toughness and abrasive resistance are good, and preparation method is simple, and production efficiency is high, and production cost Low, effects of energy saving and emission reduction is notable.
The present invention adopts the following technical scheme that to achieve these goals
A kind of dilval, its composition content by weight percentage is: ni 38-50%, c 0.8-1.5%, si 0.5-1.5%, p 0.03-0.10%, s 0.01-0.05%, cr 1-2.5%, co 0.5-1.0%, balance of iron.
The uniformity on described dilval surface is less than 5%.
The surface brightness of described dilval is one-level light.
The preparation method of described dilval, comprises the following steps:
(1) batch mixing, pressure ball: it is below 10mm that nickel oxide ores are crushed to granularity, is subsequently adding its weight 5-10% Coal dust, the bonding agent of 0.8-1.5%, the pulverized limestone of 3-5%, the water cobaltous sulfate mixing of 0.5-1.0%, are pressed into pelletizing, control Pelletizing moisture is in 8-10%;
(2) reduce: obtain metallized pellet by carrying out reduction in the pelletizing made feeding rotary hearth furnace, reduction temperature is 1300-1500 DEG C, the recovery time is 1-3 hour;
(3) melting: metallized pellet is first carried out solid-phase sintering 4-6 hour at a temperature of 1000-1350 DEG C, then proceedes to It is heated to 1500-1750 DEG C and carries out melting 1-3 hour, obtain thick dilval;
(4) refine: thick dilval is adopted aod refining furnace to refine, during refining, adds the alkalescence of its weight 2.5-3.5% Oxide, obtains smart ferronickel water, and refining temperature is 1500-1700 DEG C, and refining cycle is 30-50min/ stove, and blowing oxygen quantity is 100- 200nm3/ t, then obtain Refining Nickel ferroalloy productor through casting.
Bonding agent described in step (1) is waterglass or pva.
Basic anhydride described in step (4) are lime stone, fluorite.
Compared with the prior art, beneficial effects of the present invention are as follows:
Dilval of the present invention and preparation method thereof, the dilval density of preparation and purity are high, intensity, toughness and resistance to Mill ability is good, and preparation method is simple, and production efficiency is high, coal blending powder pelletizing in raw material, and the recovery time is short, and energy consumption is low, and dust is few, The useful element rate of recovery is high, adopts two-step sintering method during melting, controls the deformation in melting for the dilval, improves dilval Density, purity, the various performance requirements such as internal microstructure, low production cost, effects of energy saving and emission reduction is notable.
Specific embodiment
The present invention is further illustrated with reference to embodiments, but the present invention is not limited only to these embodiments, not On the premise of departing from present inventive concept, any improvement made is within the scope of the present invention.
Embodiment 1:
A kind of dilval, its composition content by weight percentage is: ni 38-50%, c 0.8-1.5%, si 0.5-1.5%, p 0.03-0.10%, s 0.01-0.05%, cr 1-2.5%, co 0.5-1.0%, balance of iron.Described The uniformity on dilval surface is less than 5%, and surface brightness is one-level light.
The preparation method of described dilval, comprises the following steps:
(1) batch mixing, pressure ball: it is below 10mm that nickel oxide ores are crushed to granularity, is subsequently adding its weight 5-10% Coal dust, the bonding agent of 0.8-1.5%, the pulverized limestone of 3-5%, the water cobaltous sulfate mixing of 0.5-1.0%, are pressed into pelletizing, control Pelletizing moisture is 8%;Described bonding agent is waterglass.
(2) reduce: obtain metallized pellet by carrying out reduction in the pelletizing made feeding rotary hearth furnace, reduction temperature is 1300 DEG C, the recovery time is 3 hours;
(3) melting: metallized pellet is first carried out solid-phase sintering 6 hours at a temperature of 1000 DEG C, then proceedes to be heated to 1500 DEG C carry out melting 3 hours, obtain thick dilval;
(4) refine: thick dilval is adopted aod refining furnace to refine, during refining, adds the alkalescence of its weight 2.5-3.5% Oxide, obtains smart ferronickel water, and refining temperature is 1500 DEG C, and refining cycle is 50min/ stove, and blowing oxygen quantity is 100nm3/ t, then warp Cross casting and obtain Refining Nickel ferroalloy productor.Described basic anhydride are lime stone, fluorite.
Embodiment 2:
A kind of dilval, its composition content by weight percentage is: ni 38-50%, c 0.8-1.5%, si 0.5-1.5%, p 0.03-0.10%, s 0.01-0.05%, cr 1-2.5%, co 0.5-1.0%, balance of iron.
The preparation method of described dilval, comprises the following steps:
(1) batch mixing, pressure ball: it is below 10mm that nickel oxide ores are crushed to granularity, is subsequently adding its weight 5-10% Coal dust, the bonding agent of 0.8-1.5%, the pulverized limestone of 3-5%, the water cobaltous sulfate mixing of 0.5-1.0%, are pressed into pelletizing, control Pelletizing moisture is 10%;Described bonding agent is pva.
(2) reduce: obtain metallized pellet by carrying out reduction in the pelletizing made feeding rotary hearth furnace, reduction temperature is 1500 DEG C, the recovery time is 1 hour;
(3) melting: metallized pellet is first carried out solid-phase sintering 4 hours at a temperature of 1350 DEG C, then proceedes to be heated to 1750 DEG C when carrying out melting 1, obtain thick dilval;
(4) refine: thick dilval is adopted aod refining furnace to refine, during refining, adds the alkalescence of its weight 2.5-3.5% Oxide, obtains smart ferronickel water, and refining temperature is 1700 DEG C, and refining cycle is 30min/ stove, and blowing oxygen quantity is 200nm3/ t, then warp Cross casting and obtain Refining Nickel ferroalloy productor.Described basic anhydride are lime stone, fluorite.

Claims (6)

1. a kind of dilval it is characterised in that: its composition content by weight percentage is: ni 38-50%, c 0.8- 1.5%th, si 0.5-1.5%, p 0.03-0.10%, s 0.01-0.05%, cr 1-2.5%, co 0.5-1.0%, balance of Iron;
The preparation method of described dilval it is characterised in that: comprise the following steps:
(1) batch mixing, pressure ball: by nickel oxide ores be crushed to granularity be below 10mm, be subsequently adding its weight 5-10% coal dust, The bonding agent of 0.8-1.5%, the pulverized limestone of 3-5%, the water cobaltous sulfate mixing of 0.5-1.0%, are pressed into pelletizing, control pelletizing water Divide in 8-10%;
(2) reduce: obtain metallized pellet by carrying out reduction in the pelletizing made feeding rotary hearth furnace, reduction temperature is 1300- 1500 DEG C, the recovery time is 1-3 hour;
(3) melting: metallized pellet is first carried out solid-phase sintering 4-6 hour at a temperature of 1000-1350 DEG C, then proceedes to heat Carry out melting 1-3 hour to 1500-1750 DEG C, obtain thick dilval;
(4) refine: thick dilval is adopted aod refining furnace to refine, during refining, adds the alkaline oxygenated of its weight 2.5-3.5% Thing, obtains smart ferronickel water, and refining temperature is 1500-1700 DEG C, and refining cycle is 30-50min/ stove, and blowing oxygen quantity is 100- 200nm3/ t, then obtain Refining Nickel ferroalloy productor through casting.
2. dilval according to claim 1 it is characterised in that: the uniformity on described dilval surface is less than 5%.
3. dilval according to claim 1 it is characterised in that: the surface brightness of described dilval be one-level light Bright.
4. a kind of preparation method of dilval as claimed in claim 1 it is characterised in that: comprise the following steps:
(1) batch mixing, pressure ball: by nickel oxide ores be crushed to granularity be below 10mm, be subsequently adding its weight 5-10% coal dust, The bonding agent of 0.8-1.5%, the pulverized limestone of 3-5%, the water cobaltous sulfate mixing of 0.5-1.0%, are pressed into pelletizing, control pelletizing water Divide in 8-10%;
(2) reduce: obtain metallized pellet by carrying out reduction in the pelletizing made feeding rotary hearth furnace, reduction temperature is 1300- 1500 DEG C, the recovery time is 1-3 hour;
(3) melting: metallized pellet is first carried out solid-phase sintering 4-6 hour at a temperature of 1000-1350 DEG C, then proceedes to heat Carry out melting 1-3 hour to 1500-1750 DEG C, obtain thick dilval;
(4) refine: thick dilval is adopted aod refining furnace to refine, during refining, adds the alkaline oxygenated of its weight 2.5-3.5% Thing, obtains smart ferronickel water, and refining temperature is 1500-1700 DEG C, and refining cycle is 30-50min/ stove, and blowing oxygen quantity is 100- 200nm3/ t, then obtain Refining Nickel ferroalloy productor through casting.
5. dilval according to claim 4 preparation method it is characterised in that: the bonding agent described in step (1) For waterglass or pva.
6. dilval according to claim 4 preparation method it is characterised in that: alkaline oxygenated described in step (4) Thing is lime stone, fluorite.
CN201510064491.0A 2015-02-06 2015-02-06 Ferro-nickel alloy and preparation method thereof Expired - Fee Related CN104630566B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201510064491.0A CN104630566B (en) 2015-02-06 2015-02-06 Ferro-nickel alloy and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201510064491.0A CN104630566B (en) 2015-02-06 2015-02-06 Ferro-nickel alloy and preparation method thereof

Publications (2)

Publication Number Publication Date
CN104630566A CN104630566A (en) 2015-05-20
CN104630566B true CN104630566B (en) 2017-01-25

Family

ID=53209809

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201510064491.0A Expired - Fee Related CN104630566B (en) 2015-02-06 2015-02-06 Ferro-nickel alloy and preparation method thereof

Country Status (1)

Country Link
CN (1) CN104630566B (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105648323A (en) * 2016-01-13 2016-06-08 铜陵百荣新型材料铸件有限公司 Ferronickel material and preparation technique thereof
CN106191433A (en) * 2016-08-12 2016-12-07 金堆城钼业股份有限公司 A kind of ball press technique of small grain size molybdenum-iron
CN107604265A (en) * 2017-10-27 2018-01-19 湖州正德轻工机械有限公司 Wear-resisting dilval
CN113528928A (en) * 2021-07-15 2021-10-22 山西太钢不锈钢股份有限公司 Iron-nickel base alloy continuous casting billet for precision strip steel and production method thereof

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101386950A (en) * 2008-10-17 2009-03-18 河北上大再生资源科技有限公司 Nickel iron intermediate alloy and melting and purification treatment method thereof
CN101495663A (en) * 2006-02-02 2009-07-29 蒂森克鲁普德国联合金属制造有限公司 Iron-nickel alloy
CN102776451A (en) * 2012-08-08 2012-11-14 山西太钢不锈钢股份有限公司 Nickel-iron spectrum standard sample and preparation method thereof

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101495663A (en) * 2006-02-02 2009-07-29 蒂森克鲁普德国联合金属制造有限公司 Iron-nickel alloy
CN101386950A (en) * 2008-10-17 2009-03-18 河北上大再生资源科技有限公司 Nickel iron intermediate alloy and melting and purification treatment method thereof
CN102776451A (en) * 2012-08-08 2012-11-14 山西太钢不锈钢股份有限公司 Nickel-iron spectrum standard sample and preparation method thereof

Also Published As

Publication number Publication date
CN104630566A (en) 2015-05-20

Similar Documents

Publication Publication Date Title
CN101748298B (en) Method for treating laterite nickel ore and producing ferronickel by combining tunnel kiln prereduction and melting furnace final reduction
CN101935794A (en) Method for producing ferro-nickel alloy by using nickel-bearing laterite in shaft furnace and smelting furnace
CN102242259B (en) Preparation process of low-grade laterite nickel ore oxidized pellet
WO2008131614A1 (en) A SMELTING METHOD OF LOW-P STAINLESS STEEL BASE USING LOW-GRADE IRONSTONE CONTAINING Ni AND Cr
CN104630566B (en) Ferro-nickel alloy and preparation method thereof
CN100424191C (en) Method for directly reducing ferronickel by tunnel kiln using laterite-nickel ore as raw material
CN105695850A (en) Utilization method of nickel-contained iron ore
CN103710543B (en) Utilize the method for producing low carbon and high silicon manganese-silicon containing manganese industrial residue two step method
CN105132674B (en) The method for preparing ferrochrome
CN107868872A (en) The method that vanadium chromium reducing slag two step method reduction melting prepares vanadium ferrochrome
CN103103347A (en) Method for preparing blast furnace ironmaking burden from full-vanadium titanium magnetite concentrate
CN102766775B (en) Production method of low-carbon high-silica silicomanganese
CN103866115B (en) The preparation of red soil nickel ore single stage method is containing the method for nickel and stainless steel raw material
CN106319124A (en) Preparing method for ferrochrome silicon alloy
CN103045790B (en) Containing nickel steel production technology
CN105463214B (en) A kind of method that high ferronickel is produced using low poor grade lateritic nickel ore
CN103757165A (en) Comprehensive valuable component utilization method of blast-furnace smelting of high iron bauxite
TW201400624A (en) Method for producing austenitic stainless steel with nickel and chromium ore
CN113957185B (en) Furnace charge formula for smelting vanadium-titanium magnetite in blast furnace
CN102010985A (en) Method for smelting ferronickel by laterite-nickel ore added by circular sintering machine-submerged arc furnace
CN103088183B (en) Method for smelting laterite-nickel ores through one-step controlled reduction
CN104651606A (en) Method for simultaneously producing iron alloy and glass ceramics by utilizing lean iron ore resources
CN101643839A (en) Method for producing ferroalloy by using pellet
CN101220438A (en) Manufacture method for directly smelting high-nickel ferronickel with low ore grade nickel materials
CN113549726B (en) Method for strengthening gas-based solid reduction of chromite

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant
TR01 Transfer of patent right

Effective date of registration: 20180814

Address after: 410000 room 24045, Zhongtian Plaza, 766 Wuyi Road, Furong district, Changsha, Hunan

Patentee after: Hunan Zhongwei Holding Group Co., Ltd.

Address before: 244199 14a24 14, Tongling big market, lion mountain area, Tongling, Anhui.

Patentee before: Tongling hundred flourish type material foundry goods company limited

TR01 Transfer of patent right
CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20170125

Termination date: 20200206

CF01 Termination of patent right due to non-payment of annual fee