CN1325688C - Abrasion-resistant corrosion-resistant material and process for preparing the same - Google Patents
Abrasion-resistant corrosion-resistant material and process for preparing the same Download PDFInfo
- Publication number
- CN1325688C CN1325688C CNB2005100863986A CN200510086398A CN1325688C CN 1325688 C CN1325688 C CN 1325688C CN B2005100863986 A CNB2005100863986 A CN B2005100863986A CN 200510086398 A CN200510086398 A CN 200510086398A CN 1325688 C CN1325688 C CN 1325688C
- Authority
- CN
- China
- Prior art keywords
- resistant
- minute
- warming
- powder
- abrasion
- 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
Links
Abstract
The present invention relates to an abrasion-resistant corrosion-resistant material and a method for preparing the abrasion-resistant corrosion-resistant material, which belong to the field of abrasion-resistant corrosion-resistant materials. 316L stainless steel powder and Y2O3 part stabilizing zirconia powder are used as raw materials, and the novel abrasion-resistant corrosion-resistant material is prepared by using the method of powder metallurgy and is composed of 316L stainless steel powder of which the content is from 30 wt% to 80 wt% and Y-PSZ powder of which the content is from 70 wt% to 20 wt%. The preparing method of the abrasion-resistant corrosion-resistant material is that the two powder raw materials are mixed with adhesive, the fully mixed powder is molded by cold press, hot degreasing is carried out on an obtained raw billet, and a degreased billet body is sintered and molded under vacuum environment or inert gas atmosphere. The present invention has the advantages of simple process, low cost, good abrasion-resistant performance, good corrosion-resistant performance, etc., and can be widely used for manufacturing abrasion-resistant corrosion-resistant components in the field of energy engineering, power machinery, chemical industry, metallurgy, aerospace, etc.
Description
Technical field
The invention belongs to wear-and corrosion-resistant material field, a kind of 316L/Y-PSZ wear-and corrosion-resistant preparation methods particularly is provided.
Background technology
Along with science and technology and high speed development of national economy, fields such as machinery, chemical industry, metallurgy are more and more higher to the requirement of wear-and corrosion-resistant material, and producing more and more becomes the important factor that influences production efficiency the work-ing life of equipping.And traditional high-abrasive material can not satisfy the requirement of application conditions gradually, therefore aspect applied research, ceramic-metal composite, engineering ceramic material and organic materials development possess excellent comprehensive performance and cheap ceramic-metal composite and solve that the material wear-resistant corrosion resisting property is required just and more preferably select rapidly.
The research of metal current ceramic composite mainly concentrate on the magnesium base, aluminium base etc. light metal-based on because it costs an arm and a leg, be mainly used in high-tech sectors such as aerospace.Wear-resistant structural part as work under high temperature, the high-speed condition, as the collars of high-speed rod-rolling mill and guide deflection sheave etc., high comprehensive performance, cheap iron and steel base wearing composite material come into one's own [open and to wait quietly. the present situation of iron base composite material and development. material Leader, 1995,1:67-71].
For improving the wear resistance of steel-based composite material, require enhanced granule in matrix, can tiny and uniformly to distribute, difficult drop-off, this point is subjected to preparation method's influence very big.The preparation method who uses mainly contains technology such as powder metallurgic method, casting infiltration, injection disperse method, casting and in-situ synthesis at present.But all there is certain deficiency in these methods, as casting infiltration, spray complex process such as disperse method and composite bed thickness is difficult to control; The subject matter of casting is easily to react between liquid metal and the particle, and the difficult control of even particle distribution; In-situ synthesis then faces do not need how to suppress the generation of reactant and the problems such as volume fraction of control enhanced granule.Though it should be noted that in the preparation of each comfortable some wearing composite material of these methods and obtained success, but applying, the scale distance also has certain distance, still need further perfect [Feng Keqin etc. the technology of preparing of iron base composite material and prospect. mechanical engineering material, 2002,26 (12): 9-13].
According to statistics, 1/3～1/2 of the energy is consumed in wearing and tearing, and 80% of material lost efficacy in wearing and tearing, if add the shut-down that manpower is changed parts, then financial loss bigger [He Jun. this year high-abrasive material development. external metallic ore ore dressing, 1996,4:21-24].Therefore, research and development excellent property, cheap iron and steel base wearing composite material have important and practical meanings.
Summary of the invention
The objective of the invention is to: a kind of 316L/Y-PSZ wear-and corrosion-resistant preparation methods is provided, and the 316L stainless steel has higher intensity, good plasticity and toughness and erosion resistance, and its thermal expansivity is about 17.5 * 10 in 20～300 ℃
-6K
-1, differ less with the thermal expansivity of yttrium oxide PSZ (Y-PSZ) pulverulent product, and the two chemical compatibility is fine, utilize the 316L/Y-PSZ matrix material of powder metallurgic method preparation, have good wear and corrosion behavior.
The present invention is by 316L powder of stainless steel and Y
2O
3PSZ Y-PSZ powder constituent, material prescription is expressed as with weight percent: 316L powder of stainless steel 30～80%, Y
2O
3PSZ Y-PSZ powder 70%～20%.The particle diameter of two kinds of powder is 0.1～100 μ m.
Preparation technology of the present invention is:
1, preparation 316L stainless steel/Y-PSZ mixed powder, 316L powder of stainless steel 30～80wt% wherein, Y-PSZ powder 70～20wt%.
2, adopt powder metallurgical technique, in the original mixed powder, add binding agent, the mixing cohesive powders of making.316L stainless steel/Y-PSZ mixed powder 90～99 weight %, binding agent 10～1 weight %.Binding agent by powdery, water-soluble Vltra tears HPMC (content be 1～10wt%) and deionized water (content is 99～90wt%) to form.HPMC has good water-solubility and viscosity, helps reducing the addition of viscosity additives, also is convenient to the compression moulding and the degreasing of blank simultaneously.With preserving at ambient temperature 12～48 hours after the cohesive powders sealing wrapping, so that its abundant maturation.Binder content can change in 1～10wt% scope.
3, cleaning die, even spraying lubricant EBS paraffin on mould inner wall reducing the frictional force in pressing process and the knockout course, thereby makes pressed density evenly and can avoid the pressed compact that causes because of frictional force is excessive in the knockout course cracked.Mixing cohesive powders after is evenly put into mould, with the pressing speed compacting of 0.1～10mm/min, is to protect under the condition of 200～600MPa to carry 1～5min moulding at pressure.
4, the pressed compact that obtains needs to carry out hot degreasing under specific technology.According to the pyrolysis temperature of each constituent element in the binding agent, take following degreasing process:
Heat-up rate with 5～10 ℃/min is warming up to 100～150 ℃, is incubated 0.5～5 hour; Heat-up rate with 5～15 ℃/min is warming up to 400～600 ℃ again, is incubated 4～8 hours.
5, the base substrate after the degreasing carries out sintering in 1200～1400 ℃ of scopes in a vacuum.Because the stainless composition of 316L is positioned at the composition range of separating out the harmful phase of fragility, if might separate out harmful fragility phase (as the σ phase) 600～900 ℃ of long-time insulations, thereby cause material structure and mis-behave, so the sintering process process should be tried one's best and fast separated out temperature range mutually through harmful fragility.
The vacuum sintering technology of taking is:
Be warming up to 300～700 ℃ with stove, be evacuated to 1.0 * 10
-1～1.0 * 10
-2Pa; Heat-up rate with 5～10 ℃/min is warming up to 900～1100 ℃; Heat-up rate with 5～10 ℃/min is warming up to 1200～1400 ℃ again, is incubated 1～3 hour; Cooling rate with 10～5 ℃/min is cooled to 900～1100 ℃; Cooling rate with 10～5 ℃/min is cooled to 600～800 ℃ again; Furnace cooling then.
The gas pressure sintering technology of taking is:
Be pumped to the stove internal gas pressure and reach 1.0 * 10
-2～50Pa; Be warming up to 300～700 ℃ with stove; Be warming up to 900～1100 ℃ with 5～10 ℃/minute heat-up rates; Be warming up to 1200～1400 ℃ with 5～10 ℃/minute heat-up rate again, be incubated 1～3 hour, filling with inert gas 1～30 minute to air pressure reaches 0.1～10MPa, heat-insulation pressure keeping 1～3 hour then; Be cooled to 900～1100 ℃ with 10～5 ℃/minute cooling rates; Be cooled to 600～800 ℃ with 10～5 ℃/minute cooling rate again; Furnace cooling then.
6, the base substrate after the degreasing also can adopt in 1200～1400 ℃ of scopes increases sintering pressure or double sintering, thermograde sintering, improves the tissue and the performance of sintered compact.
The invention has the advantages that: even particle distribution, interface are in conjunction with good and do not have the existence of thermal stresses, because the existence of hard phase Y-PSZ, the wear resisting property of material is good.Because matrix material is made up of Y-PSZ and 316L stainless steel, corrosion resisting property can reach the level identical with the 316L stainless steel simultaneously.Above-mentioned 316L/Y-PSZ high-abrasive material has higher density (＞0.97), higher microhardness (HV
0.2/15＞11GPa), higher abrasion resistance properties (under the same abrasive conditions nearly 10 times to Ni/MoS
2Matrix material).
Embodiment
Embodiment 1:316L/Y-PSZ matrix material, its material mixture ratio is: 316L/Y-PSZ mixed powder 95wt% (wherein 316L powder of stainless steel 37.9wt%, Y-PSZ powder 62.1wt%), binding agent 5wt% (wherein HPMC5wt%, water 95wt%).To preserve at ambient temperature 48 hours after the cohesive powders sealing wrapping; In mould, suppress then, reach to protect behind the pressure of 300MPa and carried 1 minute with 1mm/ minute speed; The compression moulding base substrate is put into heat treatment furnace be warming up to 100 ℃, be incubated 5 hours, be warming up to 450 ℃ with 8 ℃/minute speed then, be incubated 8 hours with 10 ℃/minute speed; Base substrate after the degreasing is warming up to 500 ℃ with stove in vacuum sintering furnace, vacuum is evacuated to 6.65 * 10
-2Pa is warming up to 1000 ℃ with 10 ℃/minute speed, is warming up to 1350 ℃ with 5 ℃/minute speed again, is incubated 2.5 hours, is cooled to 1000 ℃ with 5 ℃/minute speed then, is cooled to 800 ℃ with 10 ℃/minute speed again, then furnace cooling.
Embodiment 2:316L/Y-PSZ matrix material, its material mixture ratio is: 316L/Y-PSZ mixed powder 92wt% (wherein 316L powder of stainless steel 58.7wt%, Y-PSZ powder 41.2wt%), binding agent 8wt% (wherein HPMC10wt%, water 90wt%).To preserve at ambient temperature 24 hours after the cohesive powders sealing wrapping; In mould, suppress then, reach to protect behind the pressure of 300MPa and carried 5 minutes with 1mm/ minute speed; The compression moulding base substrate is put into heat treatment furnace be warming up to 110 ℃, be incubated 2 hours, be warming up to 450 ℃ with 8 ℃/minute speed then, be incubated 6 hours with 5 ℃/minute speed; Base substrate after the degreasing is warming up to 500 ℃ with stove in vacuum sintering furnace, vacuum is evacuated to 6.65 * 10
-2Pa is warming up to 1100 ℃ with 10 ℃/minute speed, is warming up to 1300 ℃ with 5 ℃/minute speed again, is incubated 3 hours, is cooled to 1000 ℃ with 5 ℃/minute speed then, is cooled to 800 ℃ with 10 ℃/minute speed again, then furnace cooling.
Embodiment 3:316L/Y-PSZ matrix material, its material mixture ratio is: 316L/Y-PSZ mixed powder 93wt% (wherein 316L powder of stainless steel 48.7wt%, Y-PSZ powder 51.3wt%), binding agent 7wt% (wherein HPMC7wt%, water 93wt%).To preserve at ambient temperature 36 hours after the cohesive powders sealing wrapping; In mould, suppress then, reach to protect behind the pressure of 400MPa and carried 2 minutes with 2mm/ minute speed; The compression moulding base substrate is put into heat treatment furnace be warming up to 120 ℃, be incubated 3 hours, be warming up to 500 ℃ with 10 ℃/minute speed then, be incubated 6 hours with 8 ℃/minute speed; Base substrate after the degreasing is warming up to 500 ℃ with stove in air pressure reaches the sintering oven of 14Pa, be warming up to 1000 ℃ with 10 ℃/minute speed, be warming up to 1350 ℃ with 5 ℃/minute speed again, be incubated 1.5 hours, filling with inert gas 10 minutes to air pressure reaches 9MPa then, and heat-insulation pressure keeping 1 hour is cooled to 1000 ℃ with 5 ℃/minute speed, be cooled to 800 ℃ with 10 ℃/minute speed again, then furnace cooling.
316L powder of stainless steel median size is 35 μ m in the foregoing description, and yttrium oxide PSZ Y-PSZ powder median size is 1 μ m.
To the sintering finished performance test of doing of above embodiment, Archimedes's method is adopted in the density test; Its microhardness of test on the microhardness instrument adopts 200 gram load, protects and carries 15 seconds; Compressive strength σ
BcOn material-testing machine, carry out.Test-results is as shown in table 1.
Table 1
| Embodiment | Density | HV 0.2/15(GPa) | σ bc(MPa) |
| Embodiment 1 | 98.1％ | 13.05 | 437 |
| Embodiment 2 | 97.6％ | 12.86 | 398 |
| Embodiment 3 | 97.2％ | 12.87 | 410 |
Embodiment 2 is carried out the wear resisting property test, and wear test adopts ball dish friction pair to carry out on UMT pin dish (pin-on-disc) wear testing machine.The material of the steel ball that test is used is GCr15, and diameter is 5mm.Sample is processed by embodiment two described 316L/Y-PSZ matrix materials, and diameter is Φ 27mm.Do reciprocating type Dry Sliding motion with 25Hz frequency and 8mm stroke in disc surfaces, speed is 0.05m/s, and at first running-in 3min under 2N load adds load then and continues wearing and tearing 30min to 5N, and the atmospheric environment temperature of test is 27 ℃, and relative humidity is 60%.The result contrasts as shown in table 2.
Table 2
| Sample | Frictional coefficient | Wear rate (mm/ (Nm)) |
| Embodiment 2 | 0.42 | 5.1×10 -4 |
| Ni/MoS 2Matrix material | 0.40 | 4.68×10 -3 |
Claims (3)
1, a kind of preparation 316L/Y
2O
3The method of PSZ wear-and corrosion-resistant material is characterized in that: preparation technology is:
A. prepare 316L stainless steel/Y
2O
3The PSZ mixed powder, 316L powder of stainless steel 30～80 weight % wherein, Y
2O
3PSZ powder 70～20 weight %;
B. in mixed powder, add binding agent, the mixing cohesive powders of making: 316L stainless steel/Y
2O
3PSZ mixed powder 90～99 weight %, binding agent 10～1 weight %, the content of powdery, water-soluble Vltra tears HPMC is 1～10 weight % in binding agent, the content of deionized water is 99～90 weight %; With preserving at ambient temperature 12～48 hours after the cohesive powders sealing wrapping, so that its abundant maturation;
C. the compression moulding in mould of mixing uniform cohesive powders: forming pressure is 200～600MPa, and pressing speed is 0.1～10mm/ minute, and hold time is 1～5 minute;
The parison that is pressed into that d. will obtain carries out hot degreasing, and degreasing process is: be warming up to 100～150 ℃ with 5～10 ℃/minute heat-up rates, be incubated 0.5～5 hour; Be warming up to 400～600 ℃ with 5～15 ℃/minute heat-up rate again, be incubated 4～8 hours;
E. the base substrate after the degreasing carries out vacuum sintering, and sintering process is: be warming up to 300～700 ℃ with stove, vacuum is evacuated to the limit 1.0 * 10
-1～1.0 * 10
-2Pa; Be warming up to 900～1100 ℃ with 5～10 ℃/minute heat-up rates; Be warming up to 1200～1400 ℃ with 5～10 ℃/minute heat-up rate again, be incubated 1～3 hour; Be cooled to 900～1100 ℃ with 10～5 ℃/minute cooling rates; Be cooled to 600～800 ℃ with 10～5 ℃/minute cooling rate again; Furnace cooling then.
2, preparation method according to claim 1 is characterized in that: the base substrate after the degreasing carries out gas pressure sintering, and sintering process is: be pumped to the stove internal gas pressure and reach 1.0 * 10
-2～50Pa; Be warming up to 300～700 ℃ with stove; Be warming up to 900～1100 ℃ with 5～10 ℃/minute heat-up rates; Be warming up to 1200～1400 ℃ with 5～10 ℃/minute heat-up rate again, be incubated 1～3 hour, filling with inert gas 1～30 minute to air pressure reaches 0.1～10MPa, heat-insulation pressure keeping 1～3 hour then; Be cooled to 900～1100 ℃ with 10～5 ℃/minute cooling rates; Be cooled to 600～800 ℃ with 10～5 ℃/minute cooling rate again; Furnace cooling then.
3, preparation method according to claim 1 and 2 is characterized in that: the base substrate after the degreasing adopts 1200～1400 ℃ of scopes increases sintering pressures or double sintering, thermograde sintering, improves the tissue and the performance of sintered compact.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB2005100863986A CN1325688C (en) | 2005-09-12 | 2005-09-12 | Abrasion-resistant corrosion-resistant material and process for preparing the same |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB2005100863986A CN1325688C (en) | 2005-09-12 | 2005-09-12 | Abrasion-resistant corrosion-resistant material and process for preparing the same |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1737184A CN1737184A (en) | 2006-02-22 |
| CN1325688C true CN1325688C (en) | 2007-07-11 |
Family
ID=36080126
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CNB2005100863986A Expired - Fee Related CN1325688C (en) | 2005-09-12 | 2005-09-12 | Abrasion-resistant corrosion-resistant material and process for preparing the same |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN1325688C (en) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102264938B (en) * | 2009-01-23 | 2013-05-15 | 阿尔卑斯绿色器件株式会社 | Iron-based soft magnetic alloy and dust core comprising the iron-based soft magnetic alloy |
| CN104057084A (en) * | 2013-03-20 | 2014-09-24 | 江苏天一超细金属粉末有限公司 | Water-soluble ink for printing metal and ceramic products |
| CN104059427A (en) * | 2013-03-20 | 2014-09-24 | 江苏天一超细金属粉末有限公司 | Solvent based ink for printing of metal and ceramic products |
| CN105312571A (en) * | 2015-06-17 | 2016-02-10 | 洛阳名力科技开发有限公司 | Manufacturing method for stainless steel easy to polish |
| CN116197625B (en) * | 2023-04-28 | 2023-07-21 | 安徽巨盛石油钻采配件有限公司 | Preparation process of high-pressure-resistant wear-resistant cylinder sleeve |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH04136135A (en) * | 1990-09-28 | 1992-05-11 | Toshiba Corp | High corrosion resistant and wear resistant material and its manufacture |
| CN1101737C (en) * | 1997-06-09 | 2003-02-19 | 北京科技大学 | Cosedimentation for preparing stainless steel-zirconium oxide continuous gradient functional material |
-
2005
- 2005-09-12 CN CNB2005100863986A patent/CN1325688C/en not_active Expired - Fee Related
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH04136135A (en) * | 1990-09-28 | 1992-05-11 | Toshiba Corp | High corrosion resistant and wear resistant material and its manufacture |
| CN1101737C (en) * | 1997-06-09 | 2003-02-19 | 北京科技大学 | Cosedimentation for preparing stainless steel-zirconium oxide continuous gradient functional material |
Non-Patent Citations (1)
| Title |
|---|
| Microstructure and properties of composite of stainless steel and partially stabilized zirconia Zhang Wen.quan et. al,Trans. Nonferrous Met. Soc. China,Vol.Vol. 13 No.No. 1 2003 * |
Also Published As
| Publication number | Publication date |
|---|---|
| CN1737184A (en) | 2006-02-22 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN100509693C (en) | Method for preparing micro-nano composite ceramic die material | |
| CN1321768C (en) | Preparation of warm pressed diffusing particle reinforced iron-based powder metallized composite materials | |
| CN1325688C (en) | Abrasion-resistant corrosion-resistant material and process for preparing the same | |
| CN104844178A (en) | Preparation method of self-lubricating ceramic cutting tool material comprising spherical nanometer silicon dioxide coated hexagonal boron nitride composite powder | |
| CN110819842A (en) | Preparation method of formed part based on reduced graphene oxide and copper composite material | |
| CN106119604B (en) | A kind of Y2O3Ti 8Si 1.4Zr alloys of alloying and preparation method thereof | |
| CN107513651B (en) | A kind of preparation method of titanium particle reinforced magnesium base composite material | |
| CN109811177A (en) | A kind of preparation method of highly conductive high-intensitive silver-graphene composite material | |
| WO2015066952A1 (en) | High-performance powder metallurgy stainless steel and preparation method for same | |
| CN109722605A (en) | A kind of molten infiltration combination method of powder metallurgy | |
| CN104674098A (en) | Cermet material based on TiCN-(Ti,M)CN core mixed structure and preparation method thereof | |
| CN106756599A (en) | The preparation method of cBN High Speed Steel Composites and cBN High Speed Steel Composites | |
| CN108251671A (en) | A kind of preparation method for adulterating graphene oxide enhancing ODS copper | |
| CN111531166A (en) | Method for improving sintering density of iron-based powder metallurgy part | |
| CN114318038A (en) | Boride modified Mo2FeB2Base cermet and method for preparing same | |
| CN110499442A (en) | A kind of high-strength corrosion-resistant Cr3C2Base light-weight metal ceramal and preparation method thereof | |
| CN113880557A (en) | AL2O3-cBN-based ceramic cutting tool material and method for producing the same | |
| CN113620713A (en) | WC/VCxHard material, method for the production thereof and use thereof | |
| CN109518037A (en) | A kind of Ti-18Mo-xSi alloy material and preparation method thereof of SPS preparation | |
| CN102731071A (en) | Preparation method of Al-Ti-B and rare metal synergistically-toughened alumina | |
| CN101880814B (en) | Abrasion-resistant electricity and heat conducting material and preparation method thereof | |
| CN110576176A (en) | Preparation method of high-performance diamond tool | |
| CN105369087A (en) | Bearing material resistant to high temperature | |
| CN102392149B (en) | Method for microwave sintering preparation of nano-metric rare earth modified steel-bonded hard alloy | |
| CN108975918A (en) | A kind of high tenacity high-temperature structural material MoSi2-Mo5Si3The preparation of composite ceramics |
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 | ||
| C41 | Transfer of patent application or patent right or utility model | ||
| TR01 | Transfer of patent right |
Effective date of registration: 20090515 Address after: Beijing, Xueyuan Road, Haidian District No. 30: 100083 Co-patentee after: Guangdong Fenglu Aluminium Co., Ltd. Patentee after: University of Science and Technology Beijing Co-patentee after: Foshan Sanshui Fenglu Aluminium Industry Co., Ltd. Address before: Beijing, Xueyuan Road, Haidian District No. 30: 100083 Patentee before: University of Science and Technology Beijing |
|
| CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20070711 Termination date: 20140912 |
|
| EXPY | Termination of patent right or utility model |