CN103131879A - Aluminum alloy metamorphism processing method - Google Patents

Aluminum alloy metamorphism processing method Download PDF

Info

Publication number
CN103131879A
CN103131879A CN2011103858608A CN201110385860A CN103131879A CN 103131879 A CN103131879 A CN 103131879A CN 2011103858608 A CN2011103858608 A CN 2011103858608A CN 201110385860 A CN201110385860 A CN 201110385860A CN 103131879 A CN103131879 A CN 103131879A
Authority
CN
China
Prior art keywords
alterant
melt
alloy
refining
protective gas
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.)
Pending
Application number
CN2011103858608A
Other languages
Chinese (zh)
Inventor
车云
门三泉
李祥
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.)
GUIZHOU ALUMINIUM PLANT
Original Assignee
GUIZHOU ALUMINIUM PLANT
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 GUIZHOU ALUMINIUM PLANT filed Critical GUIZHOU ALUMINIUM PLANT
Priority to CN2011103858608A priority Critical patent/CN103131879A/en
Publication of CN103131879A publication Critical patent/CN103131879A/en
Pending legal-status Critical Current

Links

Landscapes

  • Manufacture And Refinement Of Metals (AREA)

Abstract

The invention discloses an aluminum alloy metamorphism processing method. The aluminum alloy metamorphism processing method uses Na2TiO3 as alterant, and includes a step 1 of carrying out furnace refining on melt alloy, adding refining agent into the melt alloy, evenly mixing the melt alloy, and carrying out melt refining in an enclosed environment; a step 2 of carrying out gas removal operation with protective gas after refining deslagging, enabling the alterant Na2TiO3 to be added into the melt alloy in a fluidized mode along with the protective gas at the same time, carrying out stirring at the same time to enable the alterant to fully react with the melt alloy, and adding the protective gas continuously after the alterant is added until full reaction of the alterant is finished; and a step 3 of standing and regulating the temperature to 700-800 DEG C, pouring the melt alloy out of a furnace, and carrying out a next procedure. According to the aluminum alloy metamorphism processing method, the alterant has the performances of nucleus alterant and adsorption alterant, can be diffused in the melt alloy rapidly, restrain the growth of a crystal nucleus, refines material points, and is high in the utilization rate.

Description

A kind of aluminium alloy treatment process that goes bad
Technical field
The present invention relates to a kind of rotten method of aluminium alloy.
Background technology
The industrial method of rotten processing that usually adopts is come refining aluminum alloy crystal grain, and in production, alterant commonly used has type core alterant and absorption alterant.The mechanism of action of type core alterant is to add the material that some can spontaneous generation non-spontaneous nucleation in molten aluminium, makes it reach the purpose of crystal grain thinning by heterogeneous type core in process of setting.Ti is the type core alterant of commonly using, and Ti can form TiAl in aluminium liquid 3The refinement particle, thinning microstructure.The adsorptive type alterant is mainly used in the rotten processing of silumin, and its mechanism of action is that the atomic radius of alterant element is large, and solid solution capacity is little in alloy, is enriched on phase interface when crystal is grown, and hinders crystal and reaches, and can form larger constitutional supercooling again.Na is the adsorptive type alterant of commonly using, and when the aluminium alloy solution temperature dropped near the liquidus temperature of aluminium, the solubleness of sodium reduced, separate out a large amount of highly dispersed sodium colloid particles, be adsorbed in the nucleating surface of silicon, form thin film, hinder growing up of crystal, silicon crystallization condensate depression is increased.
Present industrial type core alterant adds melt mainly with the master alloy form greatly, Ti normally adds with the Al-Ti-B master alloy, use and thisly add method there are the following problems: the one, for energy-conservation unfavorable, the founding link that contains the master alloy of high density alterant element needs very high temperature (>1000 ℃); Add master alloy during aluminium alloy smelting, " dissolving " also " dilution " alterant element casts again, how this process has been equivalent to " melting-casting " link, and in master alloy, a large amount of aluminium only plays the effect that stores alterant element, and its energy that consumes is invalid fully; The 2nd, the effective element in the aluminium intermediate alloy alterant is difficult to play one's part to the full, although the matrix of master alloy is also aluminium, but when producing master alloy, the process of high-melting-point element, indissoluble solution element and aluminium generation alloying is very rambunctious, the scaling loss amount increase of the segregation of effective element, aluminium and sneaking into of a large amount of impurity, all can hardly be avoided, limiting the quantity of for impurity requires very strict high performance alloys production, and often the impurity brought into of alterant just is enough to make Chemical Composition surpass limited field; Simultaneously, under microstate, a large amount of effective alterant elements of assembling still are in homojunction colony bulk state, (<800 ℃) can't dissolve fully and melt at all at the temperature of molten aluminum, only have surface rete as thin as a wafer to play the part metamorphism owing to may producing alloying reaction with aluminium, all the other a large amount of state of aggregations are all just how to add how to exist, metamorphism thereby have a greatly reduced quality.
The adsorptive type alterant adds with the form of compound usually, and Na is that the mixture by sodium salt adds melt, and that work in mixture is NaF.This problem that adds method to exist is: the molecular weight of different sodium salts is different, add the add-on of bad control Na with mixture, and NaF is poisonous, affects the operator healthy.
Summary of the invention
The technical problem to be solved in the present invention:
For the existing problem of present aluminium alloy casting mesometamorphism method, the invention provides a kind of employing Na 2TiO 3Metamorphism treatment method as alterant.
Technical scheme of the present invention:
A kind of metamorphism treatment method of aluminium alloy uses Na 2TiO 3As alterant, specifically comprise the following steps:
Step 1: the alloy melt carries out furnace refining; Add refining agent in alloy melt, and stir, the melt refining operates in enclosed environment;
Step 2: after the refining slagging-off, with protective gas, melt is carried out the degasification operation, alterant Na2TiO3 is joined in alloy melt with protective gas in the fluidization mode; Stir simultaneously, alterant and alloy melt are fully reacted; Alterant adds complete, continues to pass into protective gas complete to the alterant reaction.
Step 3: standing, temperature adjustment to 700~800 ℃, aluminium alloy are toppled over and are come out of the stove, and enter subsequent processing.
Na 2TiO 3The add-on of alterant is the 1ppm~0.1% of furnace charge total amount.
In step 2, protective gas refers to the mixed gas of nitrogen, argon gas or nitrogen and argon gas.
Beneficial effect of the present invention:
1, save this link of making master alloy, avoided meaningless waste, reduced the smelting link.
2, Na 2TiO 3Decomposite the Ti of atomic state under molecular crystal high temperature, seed sphere of action with microcosmic micromicron level (pm), reach be beyond one's reach microtexture state and nano level (nm) state of aggregation when adding pure metal or master alloy, form the Al-Ti phase in melt, the refinement crystal improves mechanical property and the corrosion resistance nature of alloy.
3, Na 2TiO 3Decomposite the Na of atomic state under molecular crystal high temperature, as the absorption alterant, suppress the nucleus growth of silicon.
4, the alterant consumption is few, and modification effect is high, and excessive and not enough performance characteristic is obvious, thereby easily accurately grasps consumption.
5, alterant adds melt in the fluidization mode, can be diffused in rapidly and uniformly in melt, and utilising efficiency is very high.
Embodiment:
Step 1: the selected every element of according to the form below and material formula, and by the alloy total amount 1000kg for preparing, extrapolate the weight of every kind of required material.
Figure 2011103858608100002DEST_PATH_IMAGE001
Step 2: first add aluminium ingot or molten aluminum liquid in smelting furnace, heating makes it to melt fully and insulation under 700~800 ℃; Melting process is completed in enclosed environment;
Step 3: first add the selected alloying element of step 1 by formula rate again, make it dissolve fully and melt, mixed melt is stirred;
Step 4: then above-mentioned alloy melt is carried out furnace refining; Add refining agent in alloy melt, and stir, the melt refining operates in enclosed environment;
Step 5: after the refining slagging-off, with the protective gas argon gas, melt is carried out the degasification operation, make simultaneously Na 2TiO 3Join in alloy melt with the protective gas argon gas in the fluidization mode; Stir simultaneously, alterant and alloy melt are fully reacted; Alterant adds complete, continues to pass into protective gas complete to the alterant reaction.
Step 6: standing, temperature adjustment to 700~800 ℃, aluminium alloy are toppled over and are come out of the stove, and enter subsequent processing.

Claims (3)

1. the metamorphism treatment method of an aluminium alloy, is characterized in that: use Na 2TiO 3As alterant, specifically comprise the following steps:
Step 1: the alloy melt carries out furnace refining; Add refining agent in alloy melt, and stir, the melt refining operates in enclosed environment;
Step 2: after the refining slagging-off, with protective gas, melt is carried out the degasification operation, make simultaneously alterant Na 2TiO 3Join in alloy melt with protective gas in the fluidization mode; Stir simultaneously, alterant and alloy melt are fully reacted; Alterant adds complete, continues to pass into protective gas complete to the alterant reaction; Step 3: standing, temperature adjustment to 700~800 ℃, aluminium alloy are toppled over and are come out of the stove, and enter subsequent processing.
2. the metamorphism treatment method of aluminium alloy according to claim 1, is characterized in that: Na 2TiO 3The add-on of alterant is the 1ppm~0.1% of furnace charge total amount.
3. the metamorphism treatment method of aluminium alloy according to claim 1, it is characterized in that: in step 2, protective gas refers to the mixed gas of nitrogen, argon gas or nitrogen and argon gas.
CN2011103858608A 2011-11-29 2011-11-29 Aluminum alloy metamorphism processing method Pending CN103131879A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN2011103858608A CN103131879A (en) 2011-11-29 2011-11-29 Aluminum alloy metamorphism processing method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN2011103858608A CN103131879A (en) 2011-11-29 2011-11-29 Aluminum alloy metamorphism processing method

Publications (1)

Publication Number Publication Date
CN103131879A true CN103131879A (en) 2013-06-05

Family

ID=48492327

Family Applications (1)

Application Number Title Priority Date Filing Date
CN2011103858608A Pending CN103131879A (en) 2011-11-29 2011-11-29 Aluminum alloy metamorphism processing method

Country Status (1)

Country Link
CN (1) CN103131879A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105936996A (en) * 2016-06-29 2016-09-14 贵州华科铝材料工程技术研究有限公司 Aluminum alloy material replacing QT500 automobile hub and liquid forging forming method of aluminum alloy material
CN105936998A (en) * 2016-06-29 2016-09-14 贵州华科铝材料工程技术研究有限公司 Aluminum alloy material replacing QT450 automobile turbocharger shell and sand casting forming method of aluminum alloy material
CN105936995A (en) * 2016-06-29 2016-09-14 贵州华科铝材料工程技术研究有限公司 Aluminum alloy material replacing QT400 automobile control arm and semi-solid state die-casting forming method of aluminum alloy material
CN106119635A (en) * 2016-06-29 2016-11-16 贵州华科铝材料工程技术研究有限公司 A kind of replacement QT400 aluminium alloy flywheel caliper material and gravitational casting forming method thereof

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1215087A (en) * 1998-09-25 1999-04-28 清华大学 Process for preparation of titanium- and carbon-contained aluminium-base intermediate alloy
CN1312396A (en) * 2000-12-29 2001-09-12 刘庆德 Production process of fast solidified granular metal fining modifier for aluminium alloy

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1215087A (en) * 1998-09-25 1999-04-28 清华大学 Process for preparation of titanium- and carbon-contained aluminium-base intermediate alloy
CN1312396A (en) * 2000-12-29 2001-09-12 刘庆德 Production process of fast solidified granular metal fining modifier for aluminium alloy

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105936996A (en) * 2016-06-29 2016-09-14 贵州华科铝材料工程技术研究有限公司 Aluminum alloy material replacing QT500 automobile hub and liquid forging forming method of aluminum alloy material
CN105936998A (en) * 2016-06-29 2016-09-14 贵州华科铝材料工程技术研究有限公司 Aluminum alloy material replacing QT450 automobile turbocharger shell and sand casting forming method of aluminum alloy material
CN105936995A (en) * 2016-06-29 2016-09-14 贵州华科铝材料工程技术研究有限公司 Aluminum alloy material replacing QT400 automobile control arm and semi-solid state die-casting forming method of aluminum alloy material
CN106119635A (en) * 2016-06-29 2016-11-16 贵州华科铝材料工程技术研究有限公司 A kind of replacement QT400 aluminium alloy flywheel caliper material and gravitational casting forming method thereof
CN105936998B (en) * 2016-06-29 2018-06-29 贵州华科铝材料工程技术研究有限公司 A kind of replacement aluminum alloy materials of QT450 automobile turbocharger housings and its sand casting forming method
CN106119635B (en) * 2016-06-29 2018-06-29 贵州华科铝材料工程技术研究有限公司 A kind of replacement QT400 aluminium alloys flywheel caliper material and its gravitational casting forming method
CN105936995B (en) * 2016-06-29 2019-03-08 贵州华科铝材料工程技术研究有限公司 A kind of aluminum alloy materials and its semisolid pressure casting forming method substituting QT400 automobile control arm
CN105936996B (en) * 2016-06-29 2019-03-12 贵州华科铝材料工程技术研究有限公司 A kind of aluminum alloy materials and its liquid forging forming method substituting QT500 automotive hub

Similar Documents

Publication Publication Date Title
CN103981386B (en) Hypoeutectic and cocrystallized Al-Si alloy go bad and the method for refinement
Tsao Evolution of nano-Ag3Sn particle formation on Cu–Sn intermetallic compounds of Sn3. 5Ag0. 5Cu composite solder/Cu during soldering
CN102086023B (en) In-situ synthesis method combining sol-gel with thermit reaction and FeNiCrTi/NiAl-Al2O3 nano composite material synthesized by method
CN100436615C (en) Aluminum-titanium-carbon-yttrium intermediate alloy and preparing method thereof
CN102787260B (en) Preparation method of superfine crystal inoculating agent for aluminum alloy grain refinement
CN103074506B (en) Two-step charging method for preparing high-quality Al-Ti-B intermediate alloy refiner
CN102212727B (en) Authigenic quasicrystal-reinforced Mg-Zn-Y alloy and smelting method thereof
CN103361524B (en) Composite modification method for hypereutectic aluminum-silicon alloy
CN103060637A (en) Metallic hydrogen compound modified high-performance aluminum alloy material and preparation method thereof
CN104979536B (en) Lithium ion battery and its anode strip, the preparation method of active material of positive electrode
CN102333896A (en) Process for producing improved grain refining aluminium-titanium-boron master alloys for aluminum foundry alloys
CN103131879A (en) Aluminum alloy metamorphism processing method
CN101139666A (en) Method for preparing SiC particle reinforced foamed aluminium radical composite material
CN104030291A (en) Method for high-efficacy removal of phosphorus in silicon by alloy method
CN112011704B (en) Preparation method of rare earth aluminum titanium boron grain refiner
CN101876085A (en) Polycrystalline silicon ingot and preparation method thereof
CN110241342A (en) A kind of high Mn content aluminium manganese intermediate alloy and preparation method thereof
CN105132766B (en) Al-Ti-Zn intermediate alloy and preparation method thereof
CN103060628B (en) A kind of Al-Si aluminum alloy materials rotten containing P title complex and preparation method thereof
CN110273075A (en) The method for preparing high-silicon aluminium-silicon alloy using metal alum recovery crystalline silicon cutting waste material
JP2535678B2 (en) Method for producing Al-B alloy
CN114277277B (en) AlN/Al particle reinforced magnesium-aluminum rare earth based composite material and preparation method thereof
CN102000808A (en) Magnesium alloy grain refiner and grain refined magnesium alloy and preparation method of thereof
CN101886196B (en) Grain refiner for magnesium alloy and preparation method thereof
CN100467635C (en) Method for preparing aluminium-titanium-carbon master alloy

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
AD01 Patent right deemed abandoned

Effective date of abandoning: 20130605

C20 Patent right or utility model deemed to be abandoned or is abandoned