Corrosion and chemical behavior of Mg97Zn1Y2-1wt.%SiC under different corrosion solutions

To explore the corrosion properties of magnesium alloys, the chemical behavior of a high strength Mg₉₇Zn₁Y₂-1 wt.%Si C alloy in different corrosion environments was studied. Three solutions of 0.2 mol·L^-1 NaCl, Na₂SO₄ and NaNO₃ were selected as corrosion solutions. The microstructures, corrosion rate, corrosion potential, and mechanism were investigated qualitatively and quantitatively by optical microscopy(OM), scanning electron microscopy(SEM), immersion testing experiment, and electrochemical test. Microstructure observation shows that the Mg₉₇ Zn₁Y₂-1 wt.%Si C alloy is composed of α-Mg matrix, LPSO(Mg₁₂ ZnY) phase and Si C phase. The hydrogen evolution and electrochemical test results reflect that the Mg₉₇Zn₁Y₂-1 wt.%SiC in 0.2 mol·L^-1 Na Cl solution has the fastest corrosion rate, followed by Na₂SO₄ and NaNO₃ solutions, and that the charge-transfer resistance presents the contrary trend and decreases in turn.     

Corrosion and electrochemical behavior of Mg–Y alloys in 3.5% NaCl solution

The corrosion mechanism of Mg–Y alloys in 3.5% NaCl solution was investigated by electrochemical testing and SEM observation. The electrochemical results indicated that the corrosion potential of Mg–Y alloys in 3.5% NaCl solution increased with the increase of Y addition. The corrosion rate increased with the increase of Y addition because of the increase of Mg₂₄Y₅ intermetallic amounts. The corrosion gradually deteriorated with the increase of immersion time. The corrosion morphologies of the alloys were general corrosion for Mg–0.25Y and pitting corrosion for Mg–8Y and Mg–15Y, respectively. The main solid corrosion products were Mg(OH)₂ and Mg₂(OH)₃C1.4H₂O.     

Relation between corrosion behavior and microstructure of Mg-Zn-Y alloys prepared by rapid solidification at various cooling rates

The relation between corrosion resistance and microstructure of Mg-Zn-Y alloys with a long period stacking ordered (LPSO) phase has been investigated. In order to clarify the influence of microstructure evolution by rapid solidification on the occurrence of localized corrosion such as filiform corrosion, several Mg_97.25Zn_0.75Y₂ (at. %) alloys with different cooling rates were fabricated by the gravity casting, copper mould injection casting and melt-spinning techniques and their corrosion behavior and microstructures were examined by the salt immersion tests, electrochemical measurements, XRD and TEM. When the cooling rate was less than 3 × 10⁴ K s⁻¹, filiform corrosion propagated in the early stage of salt immersion test, due to formation of a massive block-shaped LPSO phase during casting. On the other hand, when the cooling rate was increased up to 3 × 10⁴ K s⁻¹, rapidly solidified (RS) alloys exhibited excellent corrosion resistance because of grain refinement and formation of a supersaturated single-phase solid solution. Large-sized Mg_97.25Zn_0.75Y₂ alloys fabricated by consolidation of the RS ribbons also exhibited excellent corrosion resistance with passivity. Enhancement of microstructural and electrochemical homogeneities in the Mg-Zn-Y alloys by rapid solidification techniques results in the passivity of substrate materials.     

Corrosion behavior of rapidly solidified Mg-Zn-rare earth element alloys in NaCl solution

Rapidly solidified flaky powder metallurgy (RS FP/M) processing was applied for preparation of corrosion-resistant bulk Mg alloys with Zn and rare earth elements. The corrosion behavior of the melt spun Mg-Zn-La and Mg-Zn-Yb alloy ribbons in 1% NaCl solution was investigated in order to determine optimum composition of corrosion-resistant Mg alloys. The effect of heat-treatment on the corrosion behavior of RS Mg-Zn-La and Mg-Zn-Yb alloys also was studied. In the Mg-Zn-La alloys, as-quenched alloys showed good corrosion resistance in the NaCl solution, but heat-treatment led to degradation due to microstructure change, that is, reduction in dispersion of the Mg₁₇La₂-type intermetallic compound. In the Mg-Zn-Yb alloys, both as-quenched and heat-treated Mg_97.5Zn_0.5Yb₂ alloys exhibited low corrosion rates because fine distribution of Mg₂Yb-type intermetallic compound in α-Mg matrix was not largely changed by heat treatment.     

Effects of cooling rate on microstructure,mechanical and corrosion properties of Mg–Zn–Ca alloy

Mg₆₉Zn₂₇Ca₄ alloys with diameters of 1.5, 2 and 3 mm were fabricated using copper mold injection casting method. Microstructural analysis reveals that the alloy with a diameter of 1.5 mm is almost completely composed of amorphous phase. However, with the cooling rate decline, a little α-Mg and MgZn dendrites can be found in the amorphous matrix. Based on the microstructural and tensile results, the ductile dendrites are conceived to be highly responsible for the enhanced compressive strain from 1.3% to 3.1% by increasing the sample diameter from 1.5 mm to 3 mm. In addition, the Mg₆₉Zn₂₇Ca₄ alloy with 1.5 mm diameter has the best corrosion properties. The current Mg-based alloys show much better corrosion resistance than the traditionally commercial wrought magnesium alloy ZK60 in simulated sea-water.     

Gd添加量对Zn-1.2Cu-1.2Mg锌合金组织和性能的影响

研究了Zn-1.2Cu-1.2Mg-xGd（x=0,0.1,0.25,0.5,质量分数,%）锌合金微观组织、在模拟体液中的腐蚀行为和力学性能。结果表明,锌合金组织主要由Zn固溶体和Mg₂Zn₁₁金属间化合物组成。当Gd添加量为0.5%时,形成了GdZn₁₂化合物。锌合金的硬度随Gd添加量的增加而增加,在0.5% Gd添加量时,硬度达到最大值为1530 MPa。在0.25% Gd添加量时锌合金具有高的抗拉伸强度,而在0.1% Gd添加量时锌合金具有最低的腐蚀速率。     

Effects of Sr on microstructure and corrosion resistance in simulated body fluid of as cast Mg–Nd–Zr magnesium alloys

Mg–2·2Nd–xSr–0·3Zr alloys (wt-%, x?=?0, 0·4, 0·7 and 2·0) were prepared by gravity casting to study the effects of Sr addition on the microstructure and corrosion resistance of Mg–Nd–Zr alloys in simulated body fluid (SBF). Phases were identified by X-ray diffraction, and microstructure was observed with optical microscopy and scanning electron microscopy. Corrosion resistance of the alloys was determined by evaluating mass loss and hydrogen evolution during immersion in SBF. Mg₁₇Sr₂ phase was formed, and the grain size decreased with additional Sr addition. For the grain refinement and more continuous second phase, which could improve the corrosion resistance, the alloy with 0·7 wt-%Sr showed the slowest corrosion rate, whereas the alloy with 2·0 wt-% showed the fastest corrosion rate due to the increased volume fraction of Mg₁₇Sr₂, which led to severe local microgalvanic corrosion.     

添加RE和Ti元素对Zn-2.5Al-3Mg合金微观结构和耐腐蚀性能的影响

采用XRD、SEM、TEM和XPS等研究了RE和Ti元素对Zn-2.5Al-3Mg合金微观结构和耐蚀性的影响。结果表明,Zn-2.5Al-3Mg合金的微观结构由富Zn相、二元共晶（Zn-MgZn₂/Mg₂Zn₁₁）和三元共晶（Zn/Al/Mg₂Zn₁₁）组成,而含有RE和Ti元素的合金中出现了新相(Ce_1-xLa_x)Zn₁₁和Al₂Ti。电化学阻抗谱表明,相对于Zn-2.5Al-3Mg合金,Zn-2.5Al-3Mg-0.1RE-0.2Ti合金的耐蚀性得到了显著的提高。XPS分析结果表明,RE元素的添加促进腐蚀产物Zn₅(CO₃)₂(OH)₆和MgAl₂O₄的形成,而RE和Ti元素的同时添加促进腐蚀产物 Zn₅(CO₃)₂(OH)₆、ZnAl₂O₄和MgAl₂O₄的形成,且都抑制了疏松多孔ZnO的生成。Zn₅(CO₃)₂(OH)₆、ZnAl₂O₄和MgAl₂O₄能够很好地粘附在试样表面,提供一层致密的保护层,从而提高Zn-2.5Al-3Mg合金的耐腐蚀性。     

Effects of Al content on the corrosion properties of Mg–4Y–xAl alloys

The corrosion performances of Mg–4Y–xAl (x = 1, 2, 3, and 4 wt%) alloys in the 3.5% NaCl electrolyte solution are investigated by electrochemical tests, weight loss measurement and corrosion morphology observation. The results indicate that corrosion modes for the alloys are localized corrosion and the filiform type of attack. With Al concentration increasing from 1 to 4 wt%, the corrosion rate of Mg–4Y–xAl alloys decreases firstly and then increases, and WA42 alloy shows the best corrosion resistance. The addition of Al element to Mg–4Y alloys leads to the formation of Al₂Y and Al₁₁Y₃ intermetallic compounds and reduces the proportion of Mg₂₄Y₅ phase. Corrosion resistance of the Mg–4Y–xAl alloys mainly depends on the size and distribution of the second phases. Besides, the addition of excessive Al can greatly consumes the Y element in the matrix, thus leading to a less protective film on the alloys. The effect of the relative Volta potential changes between the second phases and α-Mg on corrosion resistance of Mg–4Y–xAl alloys is insignificant. The main corrosion products of the Mg–4Y–xAl alloys are Mg(OH)₂, Mg₃(OH)₅Cl·4H₂O, Mg_0.72Al_0.28(CO₃)_0.15(OH)_1.98(H₂O)_0.48, and Mg₄Al₂(OH)₁₂CO₃·3H₂O.     

Enhanced corrosion performance of magnesium phosphate conversion coating on AZ31 magnesium alloy

Magnesium phosphate conversion coating (MPCC) was fabricated on AZ31 magnesium alloy for corrosion protection by immersion treatment in a simple MPCC solution containing Mg²⁺ and PO^3?₄ ions. The MPCC on AZ31 Mg alloy showed micro-cracks structure and a uniform thickness with the thickness of about 2.5 µm after 20 min of phosphating treatment. The composition analyzed by energy dispersive X-ray spectroscopy and X-ray photoelectron spectroscopy revealed that the coating consisted of magnesium phosphate and magnesium hydroxide/oxide compounds. The MPCC showed a significant protective effect on AZ31 Mg alloy. The corrosion current of MPCC was reduced to about 3% of that of the uncoated surface and the time for the deterioration process during immersion in 0.5 mol/L NaCl solution improved from about 10 min to about 24 h.     

Zn对均匀化态Mg-3Sn-Ca镁合金腐蚀性能的影响

研究了Zn元素对均匀化态Mg-3Sn-Ca合金耐腐蚀性能的影响。通过XRD、金相、SEM、失重、析氢、电化学极化曲线和阻抗谱分析了Mg-3Sn-Ca(TX31)和Mg-3Sn-Ca-Zn(TXZ311)2种合金的耐蚀性能。结果表明,Mg-3Sn-Ca合金中主要由CaMgSn及Mg₂Sn相组成,加入Zn元素后晶粒得到显著细化,第二相体积分数增加并呈弥散分布,并有Mg₂Ca相析出。而Zn的添加可显著提高Mg-3Sn-Ca合金的耐蚀性能,这主要归因于TXZ311合金具有更细小的晶粒尺寸以及均匀密集分布的CaMgSn相,使合金在腐蚀过程中形成的钝化膜更加均匀。因此,TXZ311合金的耐蚀性远高于TX31合金。     

Phase selection and performance of Mg–Cu–Y amorphous composite with different Mg/Cu ratios

In this article, Mg–Cu–Y alloys with two different Mg/Cu ratios(in at%) were prepared using a watercooled copper mold. Scanning electron microscopy and X-ray diffraction were applied to analyze the microstructure and phase composition. Moreover, corrosion resistance and wear resistance were studied systematically. The results show that both Mg65 Cu25 Y10 and Mg60 Cu30 Y10 alloys could form a composition of crystalline and amorphous phases. Although the microstructure of Mg65 Cu25 Y10 consists of an amorphous phase and a-Mg, Mg2 Cu, and Cu2 Y crystalline phases, the microstructure of Mg60 Cu30 Y10 alloy mainly consists of the amorphous phase and a-Mg, Mg2 Cu. With reducing Mg/Cu ratio, the alloys have better corrosion resistance and wear resistance. The mechanism has also been discussed in detail.     

The impact of different volume fractions of crystalline structures on the electrochemical behaviour of Mg67Zn29Ca4 alloys for biomedical applications

ABSTRACT

In this work, the influence of various volume fractions of the crystalline phase in an amorphous matrix of Mg₆₇Zn₂₉Ca₄ alloys was investigated for its corrosion resistance for biodegradable applications. An amorphous Mg₆₇Zn₂₉Ca₄ alloy was successfully fabricated using melt casting into a copper mould. Then, to obtain different ratios of the crystalline phase in an amorphous matrix, the obtained amorphous rods with 3?mm diameters were annealed at 190, 230, 250, and 400°C. The volume fraction of the crystalline phase was measured by X-ray diffraction, and the microstructures of the obtained alloys were determined based on scanning electron microscopy images. Electrochemical testing was conducted in simulated body fluid at 37°C. This report shows that the ratio of the volume fractions of amorphous and crystalline phases in alloy microstructures strongly influences their corrosion behaviours. The alloy with a fully amorphous structure was the most resistive in the analysed media.     

Effect of solid solution treatment on in vitro degradation rate of as-extruded Mg-Zn-Ag alloys

The degradation behaviors of the as-extruded and solution treated Mg-3Zn-xAg (x=0, 1, 3, mass fraction, %) alloys, as well as as-extruded pure Mg, have been investigated by immersion tests in simulated body fluid (SBF) at 37 °C. The as-extruded Mg-Zn(-Ag) alloys contained Mg₅₁Zn₂₀ and Ag₁₇Mg₅₄. While the quasi-single phase Mg-Zn(-Ag) alloys were obtained by solution treatment at 400 °C for 8 h. The quasi-single phase Mg-Zn(-Ag) alloys showed lower degradation rate and more homogeneous degradation than corresponding as-extruded Mg alloys. Degradation rate of solid-solution treated Mg-3Zn-1Ag and Mg-3Zn-3Ag was approximately half that of corresponding as-extruded Mg alloy. Moreover, the degradation rate of solid-solution treated Mg-3Zn and Mg-3Zn-1Ag was equivalent to that of as-extruded pure Mg. However, heterogeneous degradation also occurred in quasi-single phase Mg-Zn-Ag alloys, compared to pure Mg. So, preparing complete single-phase Mg alloys could be a potential and feasible way to improve the corrosion resistance.     

Effect of Ca on crystallization of Mg-based master alloy containing spherical quasicrystal

Spherical icosahedral quasicrystalline phase （I-phase） was obtained by introducing Ca into Mg-Zn-Y alloy under conventional casting conditions. Due to the addition of Ca, Mg45Zn50Yn4.5Ca0.5 primary I-phase, which is thermodynamically stable and homogeneously distributed, was generated instead of decahedral quasicrystalline phase during the solidification process; the morphology of primary I-phase in the solidification microstructure changed from petal-like one （60-80 μm） to spherical one （≤ 15 μm）. When the mass fraction of Ca reaches 0.05%, sphericalI-phase with the largest quantity, highest spheroidization rate and highest circular degree can be obtained. Meanwhile, due to the changed morphology and the decreased size of primaryI-phase, the hardness of Mg-Zn-Y-Ca master alloy is reduced. The application of spherical I-phase as particulate reinforced phase provides great opporttmities for the improvement of strength and toughness of magnesium alloys.     

A comparative study on corrosion of Mg–Al–Si alloys

Corrosion behavior of various Mg–Al–Si alloys (AS11, AS21, AS41, AS61 and AS91 series), cast under the same cooling conditions and controlled alloying composition, was investigated systematically. Optical microscopy and scanning electron microscopy were used for microstructural examinations. The corrosion behavior was evaluated by immersion tests and potentiodynamic polarization measurements in 3.5% NaCl solution. The results from both immersion tests and the potentiodynamic polarization measurements showed that marginal improvement in corrosion resistance was observed with 2.0% Al (mass fraction) containing alloy (AS21) whereas Al addition above 2.0% (AS41, AS61 and AS91) deteriorated the corrosion resistance which was attributed to β phase, acting as cathode, and the interruption of continuity of the oxide film on the surface of the alloys owing to coarsened β and Mg₂Si phases.     

Effect of Y addition on microstructure and mechanical properties of Mg–Zn–Mn alloy

The effects of Y on the microstructure and mechanical properties of Mg–6Zn–1Mn alloy were investigated. The results show that the addition of Y has significant effect on the phase composition, microstructure and mechanical properties of Mg–6Zn–1Mn alloy. Varied phases compositions, including Mg₇Zn₃, I-phase (Mg₃YZn₆), W-phase (Mg₃Y₂Zn₃) and X-phase (Mg₁₂YZn), are obtained by adjusting the Zn to Y mass ratio. Mn element exists as the fine Mn particles, which are well distributed in the alloy. Thermal analysis and microstructure observation reveal that the phase stability follows the trend of X>W>I>Mg₇Zn₃. In addition, Y can improve the mechanical properties of Mg–Zn–Mn alloy significantly, and the alloy with Y content of 6.09% has the best mechanical properties. The high strength is mainly due to the strengthening by the grain size refinement, dispersion strengthening by fine Mn particles, and introduction of the Mg–Zn–Y ternary phases.     

用球差校正扫描透射电镜研究人工时效7075铝合金的耐蚀性（英文）

使用先进的球差校正扫描透射电子显微镜研究人工时效7075铝合金耐腐蚀性增强机制。通过阻抗谱、等效电路分析、极化测量和浸泡试验,研究人工时效7075铝合金在3.5%(质量分数) NaCl溶液中的腐蚀行为。结果表明,人工时效时间越长,7075铝合金的耐腐蚀性越好。这可能归因于扫描透射电镜技术揭示的以下显微组织特征：在过时效条件下,晶界处的铜偏析有助于延缓晶间腐蚀,在Al₁₈Mg₃(Cr,Mn)₂分散体表面形成的Mg(Zn,Cu)₂沉淀有效地将作为腐蚀阴极的分散体与铝基体隔离。这项研究证明,可以通过适当的合金化和人工时效来设计耐腐蚀合金的可能性。     

The effects of heat treatment and zirconium on the corrosion behaviour of Mg-3Nd-0.2Zn-0.4Zr (wt.%) alloy

The corrosion behaviours of Mg-3Nd-0.2Zn (wt.%) (NZ) and Mg-3Nd-0.2Zn-0.4Zr (wt.%) (NZK) alloys were investigated in as-cast (F), solution-treated (T4) and artificially-aged (T6) conditions in 5% NaCl solution using immersion test and electrochemical measurements. The immersion test indicates that both NZ and NZK alloys exhibit better corrosion resistances in T4 and T6 states than in the F condition due to the galvanic corrosion between the cathodic Mg₁₂Nd compound and the anodic α matrix in the F condition. The NZK alloy demonstrates lower corrosion rates than the NZ alloy in three conditions, which indicates that the addition of zirconium has a beneficial effect on the corrosion resistance. It was discovered by field emission scanning electron microscope (FE-SEM) that the corrosion products of NZK-T6 formed in salt solution are composed of sandwich shape compounds, while that of NZ-T6 is composed of fine needle-like compounds and small particles. The former are more uniform and compact than the latter and can play a more protective role for the alloy. Electrochemical measurements also confirmed that the more protective film formed on the NZK than on the NZ alloy.     

Tensile properties of hot rolled Mg_(97)Zn_1Y_2 alloy sheets at elevated temperatures

The elevated temperature tensile properties of Mg97Zn1Y2 magnesium alloy sheets, hot rolled at 390, 420 and 450 ℃ respectively, were tested in a temperature range from room temperature to 250 ℃ with a strain rate of 1.0×10-3 s-1. The results show that the variations in yield strength for Mg97Zn1Y2 magnesium alloy sheets hot rolled at 390 ℃ and 420 ℃ with temperature resemble each other due to their similar morphology of the chain-shaped strengthening phase. The yield strength maintains at a high level of 283 MPa before 200 ℃ and decreases significantly at 250 ℃. Despite of the fine lamellar structure of Mg97Zn1Y2 magnesium alloy sheet hot rolled at 450 ℃, its yield strength decreases linearly owing to occurrence of the coarse grain, and drops to 239 MPa at 250 ℃. The elongation for all hot rolled Mg97Zn1Y2 magnesium alloy sheets increases slightly with increasing testing temperature.