CN111375875A - Duplex stainless steel overlaying layer and preparation method thereof - Google Patents
Duplex stainless steel overlaying layer and preparation method thereof Download PDFInfo
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- 229910001039 duplex stainless steel Inorganic materials 0.000 title claims abstract description 34
- 238000002360 preparation method Methods 0.000 title abstract description 5
- 239000000843 powder Substances 0.000 claims abstract description 37
- 229910045601 alloy Inorganic materials 0.000 claims abstract description 18
- 239000000956 alloy Substances 0.000 claims abstract description 18
- 238000003466 welding Methods 0.000 claims abstract description 13
- 229910001566 austenite Inorganic materials 0.000 claims abstract description 11
- 238000000034 method Methods 0.000 claims description 22
- 239000011651 chromium Substances 0.000 claims description 20
- 238000010438 heat treatment Methods 0.000 claims description 16
- 229910052804 chromium Inorganic materials 0.000 claims description 15
- 229910052750 molybdenum Inorganic materials 0.000 claims description 14
- 230000008569 process Effects 0.000 claims description 14
- 229910052757 nitrogen Inorganic materials 0.000 claims description 11
- 229910052748 manganese Inorganic materials 0.000 claims description 10
- 229910052759 nickel Inorganic materials 0.000 claims description 7
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 6
- 229910000519 Ferrosilicon Inorganic materials 0.000 claims description 4
- 229910052802 copper Inorganic materials 0.000 claims description 4
- 230000001681 protective effect Effects 0.000 claims description 4
- 229910052710 silicon Inorganic materials 0.000 claims description 4
- 229910000604 Ferrochrome Inorganic materials 0.000 claims description 3
- 229910000616 Ferromanganese Inorganic materials 0.000 claims description 3
- 229910000863 Ferronickel Inorganic materials 0.000 claims description 3
- SJKRCWUQJZIWQB-UHFFFAOYSA-N azane;chromium Chemical compound N.[Cr] SJKRCWUQJZIWQB-UHFFFAOYSA-N 0.000 claims description 3
- DALUDRGQOYMVLD-UHFFFAOYSA-N iron manganese Chemical compound [Mn].[Fe] DALUDRGQOYMVLD-UHFFFAOYSA-N 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims description 2
- 229910000734 martensite Inorganic materials 0.000 claims description 2
- 238000003756 stirring Methods 0.000 claims description 2
- 230000010355 oscillation Effects 0.000 claims 1
- 238000005260 corrosion Methods 0.000 abstract description 21
- 230000007797 corrosion Effects 0.000 abstract description 21
- 239000000203 mixture Substances 0.000 abstract description 8
- 229910018648 Mn—N Inorganic materials 0.000 abstract description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 11
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 10
- 239000011572 manganese Substances 0.000 description 9
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 9
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 8
- 239000000463 material Substances 0.000 description 8
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 6
- 239000007789 gas Substances 0.000 description 6
- 239000011733 molybdenum Substances 0.000 description 6
- 239000010935 stainless steel Substances 0.000 description 6
- 229910000963 austenitic stainless steel Inorganic materials 0.000 description 4
- 238000001816 cooling Methods 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 229910000859 α-Fe Inorganic materials 0.000 description 4
- 229910000831 Steel Inorganic materials 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 239000010959 steel Substances 0.000 description 3
- 239000010963 304 stainless steel Substances 0.000 description 2
- 229910000589 SAE 304 stainless steel Inorganic materials 0.000 description 2
- 238000005275 alloying Methods 0.000 description 2
- 238000005253 cladding Methods 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- QDOXWKRWXJOMAK-UHFFFAOYSA-N dichromium trioxide Chemical compound O=[Cr]O[Cr]=O QDOXWKRWXJOMAK-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000002161 passivation Methods 0.000 description 2
- 239000006104 solid solution Substances 0.000 description 2
- 238000005728 strengthening Methods 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
- 241001085205 Prenanthella exigua Species 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- CXOWYMLTGOFURZ-UHFFFAOYSA-N azanylidynechromium Chemical compound [Cr]#N CXOWYMLTGOFURZ-UHFFFAOYSA-N 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000004364 calculation method Methods 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
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- 238000002474 experimental method Methods 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000002715 modification method Methods 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
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- 239000002245 particle Substances 0.000 description 1
- 238000012827 research and development Methods 0.000 description 1
- 239000013535 sea water Substances 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 229910000601 superalloy Inorganic materials 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B23—MACHINE TOOLS; METAL-WORKING NOT OTHERWISE PROVIDED FOR
- B23K—SOLDERING OR UNSOLDERING; WELDING; CLADDING OR PLATING BY SOLDERING OR WELDING; CUTTING BY APPLYING HEAT LOCALLY, e.g. FLAME CUTTING; WORKING BY LASER BEAM
- B23K10/00—Welding or cutting by means of a plasma
- B23K10/02—Plasma welding
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/001—Ferrous alloys, e.g. steel alloys containing N
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/02—Ferrous alloys, e.g. steel alloys containing silicon
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- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
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- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
- C22C38/22—Ferrous alloys, e.g. steel alloys containing chromium with molybdenum or tungsten
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- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
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- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
- C22C38/38—Ferrous alloys, e.g. steel alloys containing chromium with more than 1.5% by weight of manganese
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- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
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- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
- C22C38/40—Ferrous alloys, e.g. steel alloys containing chromium with nickel
- C22C38/44—Ferrous alloys, e.g. steel alloys containing chromium with nickel with molybdenum or tungsten
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- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
- C22C38/40—Ferrous alloys, e.g. steel alloys containing chromium with nickel
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Abstract
本发明公开了一种双相不锈钢堆焊层的制备方法,包括以下步骤:使用中间合金粉按比例机械混合合金粉;使用等离子弧焊进行表面堆焊;利用固溶热处理的方法将双相不锈钢的奥氏体调节到70~80%。本发明设计了Mn‑N型双相不锈钢,实践出一种制备的方法,能有效的提高过流件的耐空蚀性能,并能大大降低过流件的防护成本。
The invention discloses a preparation method of a duplex stainless steel surfacing layer, comprising the following steps: using intermediate alloy powder to mechanically mix alloy powder in proportion; using plasma arc welding to perform surface surfacing; The austenite is adjusted to 70~80%. The invention designs the Mn-N type duplex stainless steel, and practises a preparation method, which can effectively improve the cavitation corrosion resistance of the overflow parts, and can greatly reduce the protection cost of the overflow parts.
Description
技术领域technical field
本发明涉及一种不锈钢堆焊层,尤其涉及一种双相不锈钢及其制备方法。The invention relates to a stainless steel surfacing layer, in particular to a duplex stainless steel and a preparation method thereof.
背景技术Background technique
空泡腐蚀是水工建筑和水力机械使用过程中普遍存在的一种破坏形式,是属于磨损腐蚀的一种特殊形式。它的产生原因是多相流在高速运动条件下,液体内部压力分布不均,导致液体内部产生气泡和气泡溃灭,气泡溃灭时会形成高速、高压的微射流,微射流连续不断地冲击材料表面,就会导致材料表面发生严重破坏。Cavitation corrosion is a common damage form in the use of hydraulic construction and hydraulic machinery, and it is a special form of wear and corrosion. It is caused by the uneven distribution of the internal pressure of the liquid under the condition of high-speed movement of multiphase flow, which leads to the formation of bubbles in the liquid and the collapse of the bubbles. The surface of the material will cause serious damage to the surface of the material.
双相不锈钢是不锈钢领域内重要的组成部分,它的显微组织中既包含面心立方结构的奥氏体相又包含体心立方结构的铁素体相,并且其中任一相的比例至少占有30%。正是由于双相不锈钢同时具有两相组织的结构特征,所以其性能兼具奥氏体不锈钢和铁素体不锈钢的特点。相对于铁素体不锈钢,双相不锈钢含有更多的合金元素,因此它有着全面、更好的耐腐蚀性能。在力学性能方面,因为双相不锈钢含有约一半奥氏体组织,故比铁素体不锈钢具有更好的塑性和韧性;相对于奥氏体不锈钢,双相不锈钢除了具有更高的强度外,其耐晶间腐蚀、应力腐蚀及腐蚀疲劳性能都有着明显地改善。此外,双相不锈钢还具有良好的抗点蚀、缝隙腐蚀、应力腐蚀的性能,能够与高合金奥氏体不锈钢相媲美。Duplex stainless steel is an important part in the field of stainless steel. Its microstructure contains both austenite phase of face-centered cubic structure and ferrite phase of body-centered cubic structure, and the proportion of either phase at least occupies 30%. It is precisely because duplex stainless steel has the structural characteristics of two-phase structure at the same time, so its performance has the characteristics of both austenitic stainless steel and ferritic stainless steel. Compared with ferritic stainless steel, duplex stainless steel contains more alloying elements, so it has comprehensive and better corrosion resistance. In terms of mechanical properties, because duplex stainless steel contains about half of the austenite structure, it has better plasticity and toughness than ferritic stainless steel; compared with austenitic stainless steel, duplex stainless steel has higher strength, and its The resistance to intergranular corrosion, stress corrosion and corrosion fatigue has been significantly improved. In addition, duplex stainless steel also has good resistance to pitting corrosion, crevice corrosion, and stress corrosion, which is comparable to high-alloy austenitic stainless steel.
堆焊是用焊接的方法在零件表面熔覆一层具有特定性能材料的工艺过程,其目的不是为了连接零件,而是为了使零件表面覆盖一层性能更优秀的熔覆金属,是一种经济有效的表面改性方法。Surfacing is a process of cladding a layer of materials with specific properties on the surface of parts by welding. The purpose is not to connect the parts, but to cover the surface of the parts with a layer of cladding metal with better performance. It is an economical process. Effective surface modification method.
等离子粉末堆焊是以等离子弧作为热源,应用等离子弧产生的高温将合金粉末与基体表面迅速加热并一起熔化、混合、扩散、凝固,等离子束离开后自激冷却,形成一层高性能的合金层,从而实现零件表面的强化与硬化的堆焊工艺。Plasma powder surfacing uses a plasma arc as a heat source, and the high temperature generated by the plasma arc is used to rapidly heat the alloy powder and the surface of the substrate to melt, mix, diffuse and solidify together. After the plasma beam leaves, it is self-excited and cooled to form a layer of high-performance alloy. layer, so as to realize the surfacing process of strengthening and hardening of the surface of the part.
解决水力过流部件的空泡腐蚀可从以下两方面入手 :一是开发抗空蚀综合性能更优异的新材料 ;二是利用先进的表面工程技术对过流部件表面提供防护。由于新材料的研发与制造成本非常昂贵,仅适用于大型部件和主要部件,在实际使用时,对材料表面熔覆一层性能更强的金属,既可节约贵重材料,又可对易发生空蚀破坏的部位进行具有针对性的高效防护。双相不锈钢在不同的热处理状态下性能的差异很大,将热处理调节奥氏体铁素体两相比例实际应用于空蚀服役环境的理论研究和实际应用都很少。To solve the cavitation corrosion of hydraulic overcurrent parts, we can start from the following two aspects: one is to develop new materials with better comprehensive anti-cavitation performance; the other is to use advanced surface engineering technology to provide protection for the surface of overcurrent parts. Because the research and development and manufacturing costs of new materials are very expensive, they are only suitable for large parts and main parts. In actual use, a layer of metal with stronger performance is clad on the surface of the material, which can not only save valuable materials, but also reduce the risk of voids. Targeted and efficient protection of the parts damaged by corrosion. The properties of duplex stainless steels vary greatly under different heat treatment states. There are few theoretical studies and practical applications of heat treatment to adjust the two-phase ratio of austenitic ferrite in cavitation service environments.
发明内容SUMMARY OF THE INVENTION
本发明的目的在于提供一种耐空蚀性能强的双相不锈钢堆焊层,为了实现上述目的,本发明所采取的技术方案为:The purpose of the present invention is to provide a duplex stainless steel surfacing layer with strong cavitation resistance, in order to achieve the above purpose, the technical scheme adopted in the present invention is:
一种双相不锈钢堆焊层,包括以下重量百分数的组分A duplex stainless steel surfacing layer, comprising the following components by weight percentage
C 0.02~0.04%,C 0.02~0.04%,
Cr 18.0~20.0%,Cr 18.0~20.0%,
Ni≤0.8%,Ni≤0.8%,
Mo≤0.3%,Mo≤0.3%,
N≥0.15%,N≥0.15%,
Mn≥5.0%,Mn≥5.0%,
Si 0.5~1.0%。Si 0.5~1.0%.
Fe:68.5~74.0%Fe: 68.5~74.0%
进一步的,所述双相不锈钢的PREN值≥20,其中PREN=Cr%+3.3Mo%+30N%-Mn%,其中Cr%、Mo%、N%和Mn%分别为Cr、Mo、N和Mn的重量百分含量。Further, the PREN value of the duplex stainless steel is ≥20, wherein PREN=Cr%+3.3Mo%+30N%-Mn%, wherein Cr%, Mo%, N% and Mn% are Cr, Mo, N and Mn, respectively. The weight percentage of Mn.
进一步的,所述双相不锈钢的形变诱发马氏体温度Md≥50℃,其中Md=580-520C%-2Si%-16Mn%-16Cr%-23Ni%-300N%-26Cu%-10Mo%,其中C%、Si%、Mn%、Cr%、Ni%、N%、Cu%、Mo%分别为C、Si、Mn、Cr、Ni、Cu、Mo的重量百分含量。Further, the deformation-induced martensite temperature of the duplex stainless steel Md≥50℃, wherein Md=580-520C%-2Si%-16Mn%-16Cr%-23Ni%-300N%-26Cu%-10Mo%, wherein C%, Si%, Mn%, Cr%, Ni%, N%, Cu%, and Mo% are the weight percentages of C, Si, Mn, Cr, Ni, Cu, and Mo, respectively.
本发明还提供了一种利用所述双相不锈钢堆焊层的制备方法,包括以下步骤The present invention also provides a preparation method using the duplex stainless steel surfacing layer, comprising the following steps
配置合金粉并将合金粉充分机械搅拌混合;Alloy powder is configured and fully mechanically stirred and mixed;
将混合后的合金粉加入到等离子堆焊焊机中,进行粉末堆焊,堆焊层厚度为2~3mm;The mixed alloy powder is added to the plasma surfacing welding machine for powder surfacing, and the thickness of the surfacing layer is 2~3mm;
将堆焊好的工件进行固溶热处理,固溶热处理完后,双相不锈钢堆焊层的奥氏体含量为70~80%。The surfacing welded workpiece is subjected to solution heat treatment. After the solid solution heat treatment, the austenite content of the surfacing layer of the duplex stainless steel is 70-80%.
进一步的,所述合金粉包括锰铁、铬铁、镍铁、氮化铬、铁粉、硅铁。Further, the alloy powder includes ferromanganese, ferrochromium, ferronickel, chromium nitride, iron powder, and ferrosilicon.
进一步的,所述固溶热处理温度为1000~1150℃。Further, the solution heat treatment temperature is 1000-1150°C.
进一步的,粉末堆焊过程中等离子堆焊工艺参数为Further, the plasma surfacing process parameters in the powder surfacing process are:
进一步的,所述粉末堆焊采用等离子粉末堆焊。Further, the powder surfacing welding adopts plasma powder surfacing welding.
双相不锈钢中合金元素会对其力学性能和耐腐蚀性能造成影响,本发明中的铬在耐蚀性方面起着决定性的作用。铬元素可以在钢表面形成稳定致密的Cr2O3保护膜,能够降低表面钝化的电流密度,钝化不锈钢,降低钝化状态下钢的溶解速率。同时铬还能提高钢的抗氧化性、稳定铁素体相,减少奥氏体相面积。Alloying elements in duplex stainless steel will affect its mechanical properties and corrosion resistance, and chromium in the present invention plays a decisive role in corrosion resistance. Chromium can form a stable and dense Cr2O3 protective film on the steel surface, which can reduce the current density of surface passivation, passivate stainless steel, and reduce the dissolution rate of steel in passivation state. At the same time, chromium can improve the oxidation resistance of steel, stabilize the ferrite phase, and reduce the area of the austenite phase.
镍能够控制双相不锈钢的两相平衡。通过与铬、钼协同作用,提高双相不锈钢的抗腐蚀性能。Nickel can control the two-phase equilibrium of duplex stainless steels. Through synergistic action with chromium and molybdenum, the corrosion resistance of duplex stainless steel is improved.
锰的加入可以提高双相不锈钢中氮的溶解度,并在奥氏体中发挥明显的固氮作用。The addition of manganese can improve the solubility of nitrogen in duplex stainless steel and play a significant role in nitrogen fixation in austenite.
氮是一种强奥氏体形成和稳定元素,在双相不锈钢中氮元素能有效替代镍元素,达到节约成本的目的,而且氮元素对不锈钢固溶强化、提高抗点蚀和缝隙腐蚀能力也有明显效果。Nitrogen is a strong austenite forming and stabilizing element. Nitrogen can effectively replace nickel in duplex stainless steel to save costs. Nitrogen also has solid solution strengthening and improved resistance to pitting and crevice corrosion of stainless steel. obvious effect.
钼是铁素体形成元素,在双相不锈钢中钼能和铬协同作用,提高不锈钢的抗点蚀能力。当不锈钢中的铬含量至少为18%时,钼在含氯环境中抗点蚀和缝隙腐蚀的能力是铬的三倍。但是随着钼含量的增加,双相不锈钢中σ相、χ相也跟易析出。Molybdenum is a ferrite-forming element. In duplex stainless steel, molybdenum and chromium can act synergistically to improve the pitting resistance of stainless steel. When the chromium content in stainless steel is at least 18%, molybdenum is three times more resistant to pitting and crevice corrosion than chromium in chlorine-containing environments. However, with the increase of molybdenum content, σ phase and χ phase in duplex stainless steel are also easy to precipitate.
本发明所产生的有益效果包括:本发明中的双相不锈钢配方,通过堆焊的方法熔覆在普通的金属板上,经过热处理后,耐空蚀性能优于市售2209和304不锈钢堆焊层。The beneficial effects of the present invention include: the duplex stainless steel formula in the present invention is clad on a common metal plate by surfacing, and after heat treatment, the cavitation corrosion resistance is better than that of commercially available 2209 and 304 stainless steel surfacing layers .
附图说明Description of drawings
图1 本发明中双相不锈钢堆焊层的金相组织结构图。Fig. 1 is a metallographic structure diagram of the duplex stainless steel surfacing layer in the present invention.
具体实施方式Detailed ways
下面结合附图和具体实施例对本发明做进一步详细的解释说明,但应当理解为本发明的保护范围并不受具体实施例的限制。The present invention will be further explained in detail below with reference to the accompanying drawings and specific embodiments, but it should be understood that the protection scope of the present invention is not limited by the specific embodiments.
采用等离子粉末堆焊的方法在304不锈钢板上制备双相不锈钢堆焊层具体为Mn-N型双相不锈钢堆焊层,合金粉末选用中间合金粉,具体包括锰铁、铬铁、镍铁、氮化铬、铁粉、硅铁,合金粉的主要元素含量如表1所示,表中某些元素含量使用“—”表示该元素含量过低,未检测到,粉末的粒度为100目,使用高精度的天平称量出配方所需的合金粉并机械搅拌混合在一起,为了使金属粉末均匀混合,每次搅拌的时间不小于30min,搅拌完成后将金属粉末过筛以得到粒度均匀的合金粉末,使用前放入烘箱,在70℃下烘干一小时。随后将合金粉末加入送粉器,并拧紧送粉器盖子,避免漏气导致送粉失败。The duplex stainless steel surfacing layer is prepared on the 304 stainless steel plate by the method of plasma powder surfacing, specifically the Mn-N type duplex stainless steel surfacing layer. The content of the main elements of chromium nitride, iron powder, ferrosilicon and alloy powder is shown in Table 1. In the table, the content of some elements uses "—" to indicate that the content of this element is too low and not detected. The particle size of the powder is 100 mesh. Use a high-precision balance to weigh out the alloy powder required for the formula and mix it mechanically. In order to mix the metal powder evenly, the time for each stirring is not less than 30min. Alloy powder, put into an oven before use, and dry at 70°C for one hour. Then add the alloy powder to the powder feeder, and tighten the powder feeder cover to avoid the failure of powder feeding due to air leakage.
表1 合金粉末化学成分(质量分数/%)Table 1 Chemical composition of alloy powder (mass fraction/%)
为了便于后续检测试验的开展,需要获得高质量的等离子弧堆焊层,需要合理预先选择工艺参数。等离子弧堆焊的主要工艺参数:堆焊电流、堆焊速度、送粉速度、离子气体和送粉气体流量、焊枪摆动幅度和频率、喷嘴与工件的距离等,本次等离子弧焊的工艺参数如表2所示,堆焊三次,堆焊后堆焊层总厚度5mm。In order to facilitate the development of subsequent inspection tests, it is necessary to obtain high-quality plasma arc surfacing layers, and it is necessary to reasonably pre-select process parameters. The main process parameters of plasma arc surfacing welding: surfacing current, surfacing speed, powder feeding speed, ion gas and powder feeding gas flow, welding torch swing amplitude and frequency, distance between nozzle and workpiece, etc. The process parameters of this plasma arc welding As shown in Table 2, surfacing was performed three times, and the total thickness of the surfacing layer after surfacing was 5 mm.
表2 等离子堆焊工艺参数Table 2 Plasma surfacing process parameters
焊接完成后进行固溶热处理,热处理加热方式采用随炉加热,热处理炉使用如表3所示的工艺路线,冷却时用钳子将试样从电阻炉中取出,取出后即刻放入水中冷却,冷却的过程中不停晃动试样,以避免气泡在试样周围集聚降低冷却速度,金相组织见附图1,亮白色区域为奥氏体组织,深色区域为铁素体组织,经过image pro软件的计算,奥氏体组织占比达到72.2%。After the welding is completed, solution heat treatment is carried out. The heating method of heat treatment adopts heating with the furnace. The heat treatment furnace uses the process route shown in Table 3. When cooling, the sample is taken out from the resistance furnace with pliers, and immediately after taking it out Shake the sample continuously during the process to avoid the accumulation of bubbles around the sample and reduce the cooling rate. The metallographic structure is shown in Figure 1. The bright white area is austenite structure, and the dark area is ferrite structure. After image pro According to the calculation of the software, the proportion of austenite structure reaches 72.2%.
表3 热处理工艺参数Table 3 Heat treatment process parameters
实施例2-5与实施例1的区别之处仅在于所加入的各合金粉重量不同,以使最终配置的堆焊层化学成分如表4,各合金粉使用的掺量根据所需堆焊层成分百分含量配置。The difference between Examples 2-5 and Example 1 is only that the weight of each alloy powder added is different, so that the chemical composition of the final configuration of the surfacing layer is shown in Table 4, and the amount of each alloy powder used is based on the required surfacing welding. Layer composition percentage configuration.
对照组试样为2209双相不锈钢与304奥氏体不锈钢堆焊层,采用市售焊丝TIG堆焊制备,堆焊层化学成分如表4所示,对比测试结果见表4。实施例1-5的奥氏体组织含量均在65-75%。The samples in the control group are 2209 duplex stainless steel and 304 austenitic stainless steel surfacing layers, which are prepared by TIG surfacing with commercially available welding wires. The chemical composition of the surfacing layer is shown in Table 4, and the comparative test results are shown in Table 4. The content of austenite in Examples 1-5 is all 65-75%.
表4 堆焊层化学成分(质量分数/%)Table 4 Chemical composition of surfacing layer (mass fraction/%)
表5table 5
经过点蚀浸泡和空蚀实验,本发明中的耐空蚀性能“实例”>“对比1”>“对比2”,耐点蚀性能“对比1”>“实例”>“对比2”。该种堆焊层在海水中的综合性能优秀,表现良好,耐空蚀性能比现在典型的市售的材料要优秀,且节约了镍钼铬的使用,经济效益好。After pitting immersion and cavitation corrosion experiments, the cavitation resistance performance in the present invention is "Example" > "Comparison 1" > "Comparison 2", and pitting corrosion resistance "Comparison 1" > "Example" > "Comparison 2". This kind of surfacing layer has excellent comprehensive performance in seawater, good performance, better cavitation corrosion resistance than typical commercially available materials, and saves the use of nickel, molybdenum and chromium, and has good economic benefits.
以上所述仅是本发明的优选实施方式,应当指出,对于本技术领域的普通技术人员来说,在不脱离本发明技术原理的前提下,还可以做出若干改进和变形,这些改进和变形也应视为本发明的保护范围。The above are only the preferred embodiments of the present invention. It should be pointed out that for those skilled in the art, without departing from the technical principle of the present invention, several improvements and modifications can also be made. These improvements and modifications It should also be regarded as the protection scope of the present invention.
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