CN106623863A - Preparation method of ZTA particle-reinforced steel matrix composite broken wall based on chemical method activating treatment - Google Patents
Preparation method of ZTA particle-reinforced steel matrix composite broken wall based on chemical method activating treatment Download PDFInfo
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- CN106623863A CN106623863A CN201611002238.3A CN201611002238A CN106623863A CN 106623863 A CN106623863 A CN 106623863A CN 201611002238 A CN201611002238 A CN 201611002238A CN 106623863 A CN106623863 A CN 106623863A
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- 239000002131 composite material Substances 0.000 title claims abstract description 27
- 229910000831 Steel Inorganic materials 0.000 title claims abstract description 22
- 239000010959 steel Substances 0.000 title claims abstract description 22
- 238000002360 preparation method Methods 0.000 title claims abstract description 19
- 239000000126 substance Substances 0.000 title claims abstract description 14
- 239000011159 matrix material Substances 0.000 title abstract description 12
- 238000000034 method Methods 0.000 title abstract description 3
- 230000003213 activating effect Effects 0.000 title abstract 2
- 239000002245 particle Substances 0.000 claims abstract description 68
- 150000003839 salts Chemical class 0.000 claims abstract description 39
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims abstract description 26
- 239000010936 titanium Substances 0.000 claims abstract description 25
- 229910052719 titanium Inorganic materials 0.000 claims abstract description 25
- 238000007747 plating Methods 0.000 claims abstract description 23
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims abstract description 22
- 229910052751 metal Inorganic materials 0.000 claims abstract description 14
- 239000002184 metal Substances 0.000 claims abstract description 14
- 238000001816 cooling Methods 0.000 claims abstract description 13
- 229910052759 nickel Inorganic materials 0.000 claims abstract description 11
- 238000000576 coating method Methods 0.000 claims abstract description 10
- 238000005516 engineering process Methods 0.000 claims abstract description 8
- 238000001764 infiltration Methods 0.000 claims abstract description 8
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 26
- 229910052742 iron Inorganic materials 0.000 claims description 13
- 238000010792 warming Methods 0.000 claims description 10
- 238000005266 casting Methods 0.000 claims description 9
- 239000011248 coating agent Substances 0.000 claims description 8
- 239000007788 liquid Substances 0.000 claims description 8
- 239000000463 material Substances 0.000 claims description 8
- 230000008595 infiltration Effects 0.000 claims description 7
- 239000000758 substrate Substances 0.000 claims description 7
- 238000001994 activation Methods 0.000 claims description 6
- 238000009413 insulation Methods 0.000 claims description 6
- 238000003756 stirring Methods 0.000 claims description 6
- 229910001018 Cast iron Inorganic materials 0.000 claims description 4
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims description 4
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 3
- 229910052700 potassium Inorganic materials 0.000 claims description 3
- 239000011591 potassium Substances 0.000 claims description 3
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 claims description 2
- 229910000599 Cr alloy Inorganic materials 0.000 claims description 2
- 239000001110 calcium chloride Substances 0.000 claims description 2
- 229910001628 calcium chloride Inorganic materials 0.000 claims description 2
- 239000000788 chromium alloy Substances 0.000 claims description 2
- 238000010438 heat treatment Methods 0.000 claims description 2
- 238000005245 sintering Methods 0.000 claims description 2
- 239000011780 sodium chloride Substances 0.000 claims description 2
- 238000005660 chlorination reaction Methods 0.000 claims 1
- 239000000919 ceramic Substances 0.000 description 21
- 239000012530 fluid Substances 0.000 description 4
- 239000004576 sand Substances 0.000 description 4
- 230000008901 benefit Effects 0.000 description 3
- 238000010586 diagram Methods 0.000 description 3
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 2
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 2
- 238000005299 abrasion Methods 0.000 description 2
- 235000013339 cereals Nutrition 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 230000002708 enhancing effect Effects 0.000 description 2
- 235000013312 flour Nutrition 0.000 description 2
- 238000003801 milling Methods 0.000 description 2
- 241000237970 Conus <genus> Species 0.000 description 1
- 229910001208 Crucible steel Inorganic materials 0.000 description 1
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- 229910004337 Ti-Ni Inorganic materials 0.000 description 1
- 229910011209 Ti—Ni Inorganic materials 0.000 description 1
- HZEWFHLRYVTOIW-UHFFFAOYSA-N [Ti].[Ni] Chemical compound [Ti].[Ni] HZEWFHLRYVTOIW-UHFFFAOYSA-N 0.000 description 1
- 239000003082 abrasive agent Substances 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 229910052593 corundum Inorganic materials 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 238000005265 energy consumption Methods 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- KHYBPSFKEHXSLX-UHFFFAOYSA-N iminotitanium Chemical compound [Ti]=N KHYBPSFKEHXSLX-UHFFFAOYSA-N 0.000 description 1
- 235000000396 iron Nutrition 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000004570 mortar (masonry) Substances 0.000 description 1
- 229910001000 nickel titanium Inorganic materials 0.000 description 1
- HLXZNVUGXRDIFK-UHFFFAOYSA-N nickel titanium Chemical compound [Ti].[Ti].[Ti].[Ti].[Ti].[Ti].[Ti].[Ti].[Ti].[Ti].[Ti].[Ni].[Ni].[Ni].[Ni].[Ni].[Ni].[Ni].[Ni].[Ni].[Ni].[Ni].[Ni].[Ni].[Ni] HLXZNVUGXRDIFK-UHFFFAOYSA-N 0.000 description 1
- 239000001103 potassium chloride Substances 0.000 description 1
- 235000011164 potassium chloride Nutrition 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000011435 rock Substances 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 229910001845 yogo sapphire Inorganic materials 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22D—CASTING OF METALS; CASTING OF OTHER SUBSTANCES BY THE SAME PROCESSES OR DEVICES
- B22D23/00—Casting processes not provided for in groups B22D1/00 - B22D21/00
- B22D23/04—Casting by dipping
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C33/00—Making ferrous alloys
- C22C33/006—Making ferrous alloys compositions used for making ferrous alloys
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C33/00—Making ferrous alloys
- C22C33/04—Making ferrous alloys by melting
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C28/00—Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D
- C23C28/02—Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D only coatings only including layers of metallic material
- C23C28/023—Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D only coatings only including layers of metallic material only coatings of metal elements only
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Manufacture Of Metal Powder And Suspensions Thereof (AREA)
- Crushing And Grinding (AREA)
Abstract
The invention discloses a preparation method of a ZTA particle-reinforced steel matrix composite broken wall based on chemical method activating treatment. The preparation method comprises the following steps: 1) ZTA particles are subjected to high temperature salt bath plating, and uniform titanium coatings are obtained on the surfaces of the ZTA particles; 2) nickel layers are formed at the peripheries of the titanium coatings; 3) the ZTA particles after plating are sintered, the ZTA particles are connected mutually to form a pore-shaped prefabricated body; and 4) the prefabricated body is fixed to a moulded end face or working face, then steel matrix material molten metal is cast by adopting a cast-infiltration technology, and after cooling, the ZTA particle-reinforced steel matrix composite broken wall is obtained. Active elements introduced in the preparation method can improve the interface boding property between the ZTA particles and metal, mechanical bonding between the ZTA particles and metal is changed to metallurgical bonding, and a macro bonding situation is shown in figure 1. The preparation method can improve the wear resistance of a composite, and ensures that the service life of the ZTA particle-reinforced steel matrix composite broken wall is long.
Description
Technical field
The invention belongs to high-abrasive material preparation field, and in particular to a kind of chemical activation of gyratory crusher processes ZTA
The preparation method of particle enhanced steel iron-based composite breaking wall.
Background technology
Gyratory crusher suitable for it is metallurgical, build, build the road, raw material is broken chemistry and silicate industry, according to broken
The difference and product particle of principle is of different sizes, and many models are divided into again.Cone crushing is lower than big, efficiency high, energy consumption,
Product granularity is uniform, broken and in small, broken bits various ores in being adapted to, rock.When gyratory crusher works, motor is rotated through skin
Belt wheel or shaft coupling, drive shaft of cone crusher and gyratory crusher conus portion eccentric bushing it is forced to move under make around a fixing point
Swing campaign.So that the rolled mortar wall surface being packed in adjusting sleeve is left when close during the crushing wall of crushing head,
Ore is constantly impacted in crusher chamber, extruding and flecition and realize the broken of ore.Therefore, crushing wall is circular cone
The main stressed member of disintegrating machine, in order to improve the service life of disintegrating machine, just has to improve the abrasion resistance properties of crushing wall.
Ceramic particle reinforced metal base composites had both possessed the good plasticity of parent metal and impact flexibility, easy-formation etc.
Advantage, while the high intensity, high rigidity and high-wearing feature but also with ceramic particle.When composite is worn and torn by the external world, just
Work when matrix phase is identical with enhancing in composite bed during the beginning, with the prolongation of wearing- in period, matrix phase gradually grinds off, strengthen phase
Further protect the substrate is then individually protruded, the overall wear resistance of material is improve.
The enhancing particle for preparing ceramic particle reinforced metal base composites selects ZTA ceramic particles, ZTA ceramic particles tool
There are many advantages that other particles are incomparable:First, ZTA is moderate relative to other particles that strengthen, and cost performance is high;Its
Secondary, closer to the thermal coefficient of expansion of ferrous materials, ZTA ceramic particles are used as strengthen mutually can be with for the thermal coefficient of expansion of ZTA ceramics
The composite with good thermal matching is obtained with iron-based.In addition, ZTA complex phase ceramics can be by controlling Al2O3 and ZrO2
Composition ratio, change its mechanical property and thermodynamic property parameter, such that it is able to prepare composite with different matrix phases, greatly
The range of application of ZTA complex phase ceramics is extended greatly.
But, associativity is poor between ZTA particles and iron-based, by ZTA ceramics in composite prepared by casting infiltration
Grain is combined into mechanical bond with iron-based so that ZTA ceramic particles cannot play enhanced effect.
The content of the invention
That what is invented aims to overcome that above technical problem, proposes that a kind of chemical activation processes ZTA particle reinforced irons
The preparation method of base composite breaking wall.
To achieve these goals, the present invention is adopted the following technical scheme that:
It is a kind of based on chemical activation process ZTA particle enhanced steel iron-based composite breaking walls preparation method, including with
Lower step:
1) active element titanium is mixed with inorganic salts, adding ZTA particles to stir carries out high-temperature salt bath plating, high-temperature salt bath
Temperature is 710-800 DEG C, is incubated 15-75min, obtains uniform titanium coating;
2) the ZTA particles of titanizing are inserted in chemical nickel-plating liquid, using magnetic stirrer, simultaneously heating and thermal insulation 2-6 is little
When, form nickel dam in titanium coating periphery;
3) the ZTA particles after plating are sintered, is warming up to 1200 DEG C with the programming rate of 10-15 DEG C/min from room temperature, so
Afterwards 1400 DEG C of sintering are warming up to the programming rate of 5-8 DEG C/min, along with the furnace cooling, it is prefabricated that ZTA particles are interconnected to hole shape
Body;
4) precast body is fixed on the end face or working face of casting mold, then using technology of infiltration casting cast steel substrate material gold
Category liquid, obtains ZTA particle enhanced steel iron-based composite breaking walls after cooling.
Further, step 1) in active element titanium be analytically pure titanium valve, titanium valve account for inorganic salts mass ratio be 10%-
15%.
Further, the mass fraction that ZTA particles account for titanium, inorganic salts and ZTA particle gross masses when salt bath is plated is 60%-
80%.
Further, nickel plating heating-up temperature is 70-90 DEG C.
Further, molten metal is potassium steel, chromium alloy cast iron or ni-hard cast iron.
Further, step 3) in 1400 DEG C sinter 1 hour.
Further, the inorganic salts are villaumite.
Further, the inorganic salts are sodium chloride, calcium chloride or potassium chloride.
Further, composite breaking wall is breaking wall of spindle breaker, gyratory crusher crushing wall, ring hammer crusher
Crushing wall or jaw crusher crushing wall.
Relative to prior art, the invention has the advantages that:The active element introduced in the present invention, salt bath titanizing
When titanium and ZTA ceramic grain surfaces form metallurgical binding, enhance the interfacial bonding property between titanium layer and ZTA ceramic particles, make
Combine between ZTA particles and metal and metallurgical binding is changed into from mechanical bond.ZTA ceramic particles after salt bath titanizing carry out again chemistry
Nickel plating, titanium nickel junction can generate Ti-Ni alloy, Nitinol layer serve between metallic matrix and ZTA particles one it is soft
The effect of property transition zone, greatly improves the bond strength at interface.
In the composite bed of the composite breaking wall that the present invention is prepared, metallic matrix is distributed in the hole of ZTA ceramic particles
In, when crushing wall is rubbed by foreign impacts, ZTA ceramic particles play certain protective effect to metallic matrix, so as to carry
The high abrasion resistance properties of crushing wall.
Description of the drawings
Fig. 1 is composite breaking wall schematic diagram prepared by the embodiment of the present invention 1.Wherein Fig. 1 (a) is the outer flour milling of composite breaking wall
Schematic diagram, Fig. 1 (b) is flour milling schematic diagram in composite breaking wall.
Specific embodiment
The present invention is described in further detail with reference to embodiment.
Embodiment 1:Breaking wall of spindle breaker
1) titanium valve is mixed with inorganic salts, adding ZTA particles to stir carries out high-temperature salt bath plating, and high-temperature salt bath temperature is
750 DEG C, 15min is incubated, obtains homogeneous coating;Wherein, the mass ratio that titanium valve accounts for inorganic salts is 10%, and ZTA is ceramic when salt bath is plated
Mass fraction shared by particle is 80%.
2) the ZTA particles of titanizing are inserted in chemical plating fluid, using magnetic stirrer and be heated to 70 DEG C insulation 2
Hour, obtain nickel dam;
3) the ZTA particles after plating are sintered, is warming up to 1200 DEG C with the programming rate of 10-15 DEG C/min from room temperature, so
It is warming up to 1400 DEG C with the programming rate of 5-8 DEG C/min afterwards to sinter 1 hour, along with the furnace cooling, ZTA particles are interconnected to hole shape
Precast body;
4) precast body is fixed in sand mold, then steel substrate material metal liquid is poured into a mould using technology of infiltration casting, after cooling
ZTA particle enhanced steels iron-based composite breaking wall (breaking wall of spindle breaker) shown in Fig. 1 is obtained, after chemical activation process
ZTA ceramic particles 1 are distributed on metallic matrix 2.
Embodiment 2:Gyratory crusher crushing wall
1) titanium valve is mixed with inorganic salts, adding ZTA particles to stir carries out high-temperature salt bath plating, and high-temperature salt bath temperature is
780 DEG C, 30min is incubated, obtains homogeneous coating;Wherein, the mass ratio that titanium valve accounts for inorganic salts is 15%, and ZTA is ceramic when salt bath is plated
Mass fraction shared by particle is 72%.
2) the ZTA particles of titanizing are inserted in chemical plating fluid, using magnetic stirrer and be heated to 76 DEG C insulation 4
Hour, obtain nickel dam;
3) the ZTA particles after plating are sintered, is warming up to 1200 DEG C with the programming rate of 10-15 DEG C/min from room temperature, so
It is warming up to 1400 DEG C with the programming rate of 5-8 DEG C/min afterwards to sinter 1 hour, along with the furnace cooling, ZTA particles are interconnected to hole shape
Precast body;
4) precast body is fixed in sand mold, then steel substrate material metal liquid is poured into a mould using technology of infiltration casting, after cooling
Obtain the compound gyratory crusher crushing wall of ZTA particle enhanced steels iron-based.
Embodiment 3:Ring hammer crusher crushing wall
1) titanium valve is mixed with inorganic salts, adding ZTA particles to stir carries out high-temperature salt bath plating, and high-temperature salt bath temperature is
710 DEG C, 45min is incubated, obtains homogeneous coating;Wherein, the mass ratio that titanium valve accounts for inorganic salts is 12%, and ZTA is ceramic when salt bath is plated
Mass fraction shared by particle is 68%.
2) the ZTA particles of titanizing are inserted in chemical plating fluid, using magnetic stirrer and be heated to 85 DEG C insulation 6
Hour, obtain nickel dam;
3) the ZTA particles after plating are sintered, is warming up to 1200 DEG C with the programming rate of 10-15 DEG C/min from room temperature, so
Rise to 1400 DEG C with the programming rate of 5-8 DEG C/min afterwards to sinter 1 hour, along with the furnace cooling, it is pre- that ZTA particles are interconnected to hole shape
Body processed.
4) precast body is fixed in sand mold, then steel substrate material metal liquid is poured into a mould using technology of infiltration casting, after cooling
Obtain TA particle enhanced steel iron-based complex loop hammer mill crushing walls.
Embodiment 4:Jaw crusher crushing wall
1) titanium valve is mixed with inorganic salts, adding ZTA particles to stir carries out high-temperature salt bath plating, and high-temperature salt bath temperature is
800 DEG C, 60min is incubated, obtains homogeneous coating;Wherein, the mass ratio that titanium valve accounts for inorganic salts is 13%, and ZTA is ceramic when salt bath is plated
Mass fraction shared by particle is 60%.
2) the ZTA particles of titanizing are inserted in chemical plating fluid, using magnetic stirrer and be heated to 90 DEG C insulation 8
Hour, obtain nickel dam;
3) the ZTA particles after plating are sintered, is warming up to 1200 DEG C with the programming rate of 10-15 DEG C/min from room temperature, so
Rise to 1400 DEG C with the programming rate of 5-8 DEG C/min afterwards to sinter 1 hour, then along with the furnace cooling, ZTA particles are interconnected to hole
Shape precast body;
4) precast body is fixed in sand mold, then steel substrate material metal liquid is poured into a mould using technology of infiltration casting, after cooling
Obtain the compound jaw crusher crushing wall of TA particle enhanced steels iron-based.
Claims (9)
1. a kind of preparation method of the ZTA particle enhanced steel iron-based composite breaking walls based on chemical activation process, its feature exists
In comprising the following steps:
1) active element titanium is mixed with inorganic salts, adding ZTA particles to stir carries out high-temperature salt bath plating, high-temperature salt bath temperature
For 710-800 DEG C, 15-75min is incubated, obtains uniform titanium coating;
2) the ZTA particles of titanizing are inserted in chemical nickel-plating liquid, using magnetic stirrer and heating and thermal insulation 2-6 hours,
Nickel dam is formed in titanium coating periphery;
3) by after plating ZTA particles sinter, be warming up to 1200 DEG C with the programming rate of 10-15 DEG C/min from room temperature, then with
The programming rate of 5-8 DEG C/min is warming up to 1400 DEG C of sintering, and along with the furnace cooling, ZTA particles are interconnected to hole shape precast body;
4) precast body is fixed on the end face or working face of casting mold, then steel substrate material metal is poured into a mould using technology of infiltration casting
Liquid, obtains ZTA particle enhanced steel iron-based composite breaking walls after cooling.
2. preparation method according to claim 1, it is characterised in that:Step 1) in active element titanium be analytically pure titanium
Powder, it is 10%-15% that titanium valve accounts for the mass ratio of inorganic salts.
3. preparation method according to claim 1, it is characterised in that:ZTA particles account for titanium, inorganic salts and ZTA when salt bath is plated
The mass fraction of particle gross mass is 60%-80%.
4. preparation method according to claim 1, it is characterised in that:Nickel plating heating-up temperature is 70-90 DEG C.
5. preparation method according to claim 1, it is characterised in that:Molten metal is potassium steel, chromium alloy cast iron or nickel
Hard cast iron.
6. preparation method according to claim 1, it is characterised in that:Step 3) in 1400 DEG C sinter 1 hour.
7. preparation method according to claim 1, it is characterised in that:The inorganic salts are villaumite.
8. preparation method according to claim 1, it is characterised in that:The inorganic salts are sodium chloride, calcium chloride or chlorination
Potassium.
9. preparation method according to claim 1, it is characterised in that:Composite breaking wall is breaking wall of spindle breaker, rotation
Return formula crusher in crushing wall, ring hammer crusher crushing wall or jaw crusher crushing wall.
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CN109513905A (en) * | 2018-12-28 | 2019-03-26 | 西安交通大学 | A kind of preparation method being surface-treated the iron-based composite wear-resistant part of ZTA particle enhanced steel |
CN109706438A (en) * | 2018-12-28 | 2019-05-03 | 西安交通大学 | A kind of preparation method of the modified ZTA ceramic particle enhancing steel-based composite material in surface |
CN110629106A (en) * | 2019-11-08 | 2019-12-31 | 沈阳工业大学 | Method for reinforcing nodular cast iron material by using nano SiO2 particles |
CN112589095A (en) * | 2020-12-11 | 2021-04-02 | 西安交通大学 | High-flux preparation method of gravity-infiltrated iron-based composite material preform |
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