This invention relates to an aluminium based alloy for manufacture of cast parts which display enhanced fracture resistance.
Typical alloys for high pressure diecasting (HPDC) are based around the Al—Si alloying system, with a range of additive elements present. Some common HPDC alloys from different regions of the world and their compositions are shown in Table 1. More recently however, there has been a range of alloy compositions developed for high ductility such as the five specialty alloys Magsimal, Silafont, Aural 2, 367.0 and 368.0, and each of these has found application in components used in crash sensitive applications where high energy absorption is required. The compositions of these alloys are shown in Table 2. These specialty alloys generally display levels of ductility between 8 and 20% in the as-cast conditions. Some common features of these three alloys are as follows:
Silafont, Aural 2, 367 and 368 are similar and based around the Al—Si system, whereas Magsimal is based on the Al—Mg alloying system. However, several of the alloys of Table 2 also are required to have low contents of Zn, which may also assist in avoiding the formation of Zn vapour porosity in the components. Generally, these three alloys also preferably are produced using vacuum diecasting, to reduce porosity that can be considered detrimental to ductility.
All of the above features 1 to 4 are known to assist in improving ductility of other HPDC alloys. Furthermore it should be noted that iron and manganese are present in HPDC alloys to minimize die soldering (sticking) so that die life is increased and productivity is improved. In general, the Fe content needs to be above 0.5% to avoid soldering, but can be substituted by other elements such as Mn, as in the case of the specialty alloys mentioned. In other cases, Sr may be used for the prevention of die soldering. However, Fe allowances are preferred because a large proportion (estimated at greater than 95%) of HPDC alloys are made of secondary metal. Additionally, Fe tends to accumulate during recycling operations, and, as a result, is an important factor to be considered in the development of alloys. Fe, Mn and Cr tend to form intermetallics that will be present in differing amounts and morphologies, depending on the so-called “sludge factor” of the alloy. In high pressure diecasting, a proportion of sludge particles form in the melt, some in the shot sleeve, and some during solidification in the die. Generally, a simple rule to be followed is that:
Sludge factor (SF)=(1×wt % Fe)+(2×wt % Mn)+(3×wt % Cr),
where SF less than 1.7 is generally considered to be most acceptable in practice. Cr is purposefully omitted in most compositions worldwide, due to its toxicity. It can however sometimes be present as a minor impurity. When no Cr is present, the relationship is then:
SF=(1×wt % Fe)+(2×wt % Mn)
The morphology of the sludge particles is strongly influenced by the Fe:Mn:Cr ratio of the alloy, and because of this, Mn and Cr are sometimes referred to as Fe correctors since they can eliminate a proportion of the undesirable, needle-like Fe—Al intermetallic phases within the alloy, causing the Fe—Al intermetallics to form more innocuous particle morphologies such as star-like rosettes, blocky shaped, Chinese script or polyhedral particles. In general, it is the Chinese script morphology that is considered to be most desirable. However, the Chinese script form is generally associated with additions of Cr, which is now purposefully omitted from most alloy specifications due to toxicity concerns. Although other transition metal elements (for example Co, Ni, V) may also serve as Fe correctors, Mn is the most common in commercial alloy products since it often appears in alloys produced by recycling. When the ratio of Fe:(Mn+Cr) is high, the sludge particles tend to be needle-like. When the ratio of Fe:(Mn+Cr) is low, the particles tend to exhibit more Chinese script, blocky, star-like or polyhedral particles. In general, the recommended amounts of Fe correctors are of the order of half the concentration of Fe. However, adding Fe correctors to an alloy also increases the total fraction of hard, brittle particles that may be detrimental to machining, fracture resistance and ductility of the alloy. Some sludge particles may also be more detrimental than needle-like particles to fracture resistance (e.g. star like or rosette shaped) when they are present in larger amounts because they may behave as large brittle plates. The size, shape and distribution of these particles are therefore very important.
Although ductility and fracture resistance may both be affected by similar microstructural features, they are not necessarily directly related, and high ductility does not necessarily mean high fracture resistance. A survey of the literature concerning the fracture properties of HPDC products has revealed that little information exists, with the exception of a limited amount of data on Charpy impact energy. It has also become a widely accepted practice in the design of HPDC products to rely solely on tensile elongation as a measure of fracture resistance. However, neither Charpy impact energy nor tensile ductility is considered in scientific literature to be a valid indicator of the comparative fracture toughness properties of different aluminium alloys. Although alloys which have high ductility may often show high fracture resistance, similar alloys with lower tensile ductility may also display high fracture resistance. Similarly, for a specific ductility value, fracture resistance may vary from alloy to alloy. Fundamental to solving this dilemma therefore is the acquisition of valid fracture toughness data.
HPDC products typically approximate to either a single projected plate or a series of interconnected plates. Such castings have a nearly constant wall thickness, often 2 to 6 mm. There are, however, exceptions when locally increased section thickness is required to increase stiffness, to improve metal feeding during casting or to allow for geometric features such as bolt holes and most parts display varying thickness as well as geometric stress raisers. Such changes in thickness or geometric stress raisers may approximate to a notch within the material, which then influences the overall performance of the product in service. As may be appreciated, it is rare to have applications that fail by a purely tensile mode.
ASTM standard B871 describes a method for comparative evaluation of fracture resistance using a technique developed specifically for testing wrought aluminium sheet and plate materials, which is also an acceptable representation of fracture resistance for cast aluminium alloys. The technique also provides an estimate of the notch sensitivity of the material. In general, the tear test method of ASTM standard B871 provides load displacement curves relating to crack initiation and propagation. The area of initiation up to the point of maximum loading when cracking begins, as well as the area of propagation under the curve describes the entire fracture process as it relates to thin plates. The maximum load obtained during the testing of ASTM B871 may be used to determine the tear strength of the material. The ratio of the tear strength to the yield strength (0.2% proof stress) or TYR (Tear to Yield ratio) value gives a measure of notch sensitivity.
The area under the whole curve provides the unit total energy, and the area from the peak load to the end of cracking gives the unit propagation energy. Results are presented along with tensile data (0.2% proof stress, tensile strength, ductility) taken from the same material batch. The inherent reliability of the tear test method has also been shown to provide reasonable correlations with other fracture toughness data such as the critical strain energy release rate Gc.
As might be expected, the fracture resistance of HPDC products is related to a range of failure types. For example, when a fatigue crack reaches a critical length during service, conditions for rapid and uncontrollable fracture may result. As a result, it has also been shown that, at least in some wrought alloys, there is a relationship between the unit propagation energy derived from the tear test, and the rate of crack growth in fatigue. This is not altogether unexpected, since increased fracture toughness may also correspond to improved fatigue resistance.
Optimally, a HPDC component is utilized in the as-cast state. However, there is a range of thermal processes that may be applied to a HPDC alloy. For example, in patent application WO2006/066314, methods are shown by which conventionally produced HPDC alloys and components may be successfully heat treated without displaying surface blistering or dimensional instability, and a range of heat treatments has been demonstrated that take advantage of the procedures disclosed in application WO2006/066314.
The present invention utilises an aluminium based casting alloy which provides high fracture resistance mostly irrespective of the ductility of the alloy, although high ductility in the alloy is an additional advantage in the alloy when casting quality is improved. The alloy is applicable to castings in which porosity may be present. Castings of the alloy may be produced by what can be regarded as a conventional or usual die casting technique, such as with a cold-chamber die casting machine. The castings may be produced with or without either an applied vacuum or use of a reactive gas. The castings may alternately be produced by high integrity casting processes to achieve minimum levels of porosity.
An aluminium based alloy utilised in the invention has a weight percentage composition of:
The alloy preferably is free of beryllium, rare earth elements and transition metal elements other than those individually identified (that is, other than Ti, Mn, Fe, Cu and Zn).
According to the invention, there is provided a HPDC casting having enhanced fracture resistance relative to casting of the same product made of a conventional HPDC alloy when compared in the as cast or same heat treated state, wherein the HPDC casting having enhanced fracture resistance has a weight percentage composition of:
wherein the limits for iron and manganese are constrained such that the amount of iron present in the alloy is 0.4 to 1.6 times the manganese content and the casting composition has a sludge factor (SF), calculated as SF=(1×wt % Fe)+(2×wt % Mn), of from 0.8 to 1.6; and
wherein the casting having enhanced fracture resistance has a microstructure exhibiting silicon present in solidified eutectic, with the eutectic also containing iron-bearing phases consisting substantially of fine polyhedral particles.
The microstructure of the casting is able to be substantially free of acicular silicon particles.
The casting preferably is free of beryllium, rare earth elements and transition metal elements other than those individually identified (that is, other than Ti, Mn, Fe, Cu and Zn).
The role of each of the elements of both the alloy and the manufacture of the casting of the invention now will be discussed in turn.
Silicon is required in the alloy to depress the melting temperature, aid fluidity and increase strength. Compositions ranging from hypoeutectic through to hypereutectic are applicable within the limits of 5 to 15%, but all require good fluidity to aid casting. The Si level preferably is from 6.5 to 10.5% and more preferably from 6.5 to 8.5%.
This corresponds to the optimal casting conditions for the majority of instances. Below the lower limits of Si content, castability may be adversely affected. Above the upper limits of Si content, the high proportion of the Si phase produces proportionately higher embrittling effects and reduced resistance to crack propagation.
Copper is present to also aid fluidity and to provide strengthening to the alloy, optionally by heat treatment, where required. In general, Cu levels around 1.5 to 3 wt% are optimal in the present invention, but levels as low as 1% and as high as 4% may also be considered suitable in some applications. Below 1% Cu, any heat treatment response will be limited, and above 4% Cu, embrittling effects arising from residual Cu-based intermetallics may be evident. Additionally, these Cu-based intermetallics may adversely influence corrosion resistance. Higher levels of Cu may also incur a cost penalty.
Iron and manganese concentrations are interrelated. Although some Cr, rare earth elements or other transition metals may be as functional in practice as Mn, their presence should be restricted or reduced to trace element levels wherever possible to promote the formation of (Al15(Mn,Fe)3Si2 in a fine polyhedral form. Due to toxicity concerns regarding Cr, it is preferable to limit Cr content to a minimum. Because of this, the correct proportions and amounts of both Fe and Mn are required. Following the general rule for sludge factor (SF) of the alloy, for the purpose of the present invention, SF=0.8 to 1.6=(1×Fe)+(2×Mn), and preferably SF=1.0 to 1.3. This ensures good castability, no die sticking and the presence of the correct forms of intermetallic phases. As a result of this sludge factor limitation and that of the alloy composition, the relative amounts of Fe and Mn for the invention are readily determined. If Fe content is proportionately high compared to Mn, the alloy tends to form distributed particles of FeSiAl5 which are present as needles in the microstructure. If the Mn content is proportionately high compared to Fe, the alloy may more readily exceed the sludge factor limits or not form the appropriate morphology of hard particles.
Ideally, the Fe content should be 0.4 to 1.6 times the Mn content by weight, and most preferably 0.5 to 0.9 times, within the scope of the compositional limitations and sludge factor limits. For example, if 0.4% Mn is present in the alloy, then 0.4 times the Mn content gives minimum Fe content of 0.16% with an alloy sludge factor of 0.96. 1.6 times the Mn content gives 0.64% Fe, but there is a maximum Fe allowance of 0.6% to give an alloy sludge factor of 1.4. If the alloy contains 0.6% Fe, then the minimum Mn allowable is 0.375% and the maximum content of Mn permitted is 0.5%, in order to stay within the limits of the sludge factor maximum of 1.6. In the present invention, these ratios and limitations positively influence the microstructure that develops both in the as-cast and heat treated conditions by promoting the formation of innocuous transition metal containing intermetallic particles that are polyhedral rather than plate or needle like in shape.
The Fe content preferably ranges from 0.2 to 0.4%, while the Mn content preferably is from 0.3 to 0.6%.
Rare earth metals are reported to provide both Fe modification and Si modification, but they are preferably omitted from the present invention, due to toxicity, cost and availability. Trace amounts of rare earth elements may however, be present in secondary aluminium alloys where contamination has arisen from other sources. The rare earth elements, combined with other transition metals, should be kept below 0.2% in total.
Strontium is known as a modifier to silicon in cast aluminium alloys. However, it's presence is not necessary in the present invention to promote modification and eliminating it from the alloy has various benefits, such as avoiding the potential formation of Sr—Fe intermetallic compounds which will increase relative sludge content. Sr also is known to increase porosity in aluminium castings. Similarly, Na, Ca and P are omitted or kept to very low levels. Use of any of these four elements as purposeful additions provides a cost penalty associated with the use of master alloys typically utilized, but Sr in particular may appear as trace amounts if alloy is manufactured from recycled material. In this case, the combined levels of silicon modifying elements should be kept at a level below 0.01 wt %, with strontium below 0.007 wt %.
Titanium may be present in small quantities, of up to 0.25%, as an optional element but it is not necessary for the efficacy of the present invention. Above this limit, Ti will form coarse sludge particles which may be detrimental to fracture resistance.
Zinc may be present at levels up to 3%, but its presence is not necessary for the functionality of the invention. Zinc may be present to improve castability, machinability or corrosion resistance in the alloy and optimally, may be 0.3 to 1.0%. Elevated Zn contents such as up to 3% may arise due to the presence of Zn diecast material in recycling operations, but higher levels should be avoided where possible due to the high vapour pressure of Zn resulting in additional gas phase porosity in castings.
Tin should be omitted within the alloy of the invention, or restricted to trace element levels as specified. Tin may have a detrimental effect on the shape of Fe-containing intermetallic particles causing them to form rosettes comprised of brittle phases. Tin may also cause severe problems with die sticking and hot tearing, even when present at very low levels.
Magnesium is often present simply as an impurity in high pressure diecasting alloys which contain Cu. It may however increase strength and modify the precipitation occurring in the alloy during cooling following casting or during heat treatment. At the lower limits, ˜0.05% Mg is required to initiate an age hardening response in HPDC alloys. Higher Mg levels (e.g. greater than 0.2 wt %) lead to progressive reductions in fracture resistance.
Beryllium is known to provide various advantages to aluminium alloys. It is however highly toxic and expensive and should therefore not be permitted or included in the alloy other than trace, incidental amounts which may arise due to the use of secondary metal.
By the manufacture of the abovementioned alloy, it may be appreciated that due to the generous Fe allowance, that the alloy may be manufactured by blends or proportions of secondary alloys. Similarly, as the alloy is similar to the broad specifications of many alloys utilized worldwide, it may be readily recycled with other secondary material without segregation. As may be appreciated, it may also be recycled into alloy within the limits of the alloy composition of the present invention.
The sludge factor SF, as detailed above, generally is taken as:
SF=(1×wt % Fe)+(2×wt % Mn)+(3×wt % Cr),
although Cr usually is not present as more than a minor impurity, such that effectively:
SF=(1×wt % Fe)+(2×wt % Mn).
In the present invention, Cr is constrained by the requirement that transition metal elements other than Ti, Mn, Fe, Cu and Zn, plus rare earth metals, are present at less than 0.2 wt % in total. As a practical matter, that limit of less than 0.2 wt % constrains the Cr content to a sufficiently low level at which its influence in raising the sludge factor can generally be disregarded. That is, given that any Cr present will be accompanied by other metals subject to the limit of less than 0.2 wt % in total, the Cr content will be sufficiently low. However, it generally is desirable that the content of Cr alone is less than 0.05 wt %, such as below 0.02 wt %.
The alloy of the present invention is most highly suited to the process of high pressure diecasting, but may also be utilized on other casting techniques such as squeeze casting or thixo-casting. There is also the possibility that the current alloy may also be suitable for permanent mold casting or sand casting.
a) shows the configuration of the plate shaped castings used for tear test development purposes with the alloy of the present invention;
b) shows a tear test fracture sample and a tensile sample taken from castings as in
The curves of
a) shows the configuration of the plate shaped castings used for tear test development purposes with the alloy of the present invention, as well as the runner system, overflows and ejector pin positions. The dimensions of the plates are 70 mm wide, 60 mm long and approximately 2 mm thick. From these and in accordance with the standard, one tear test fracture sample and one tensile sample were taken from each plate (
The samples were oriented either with the propagating crack running parallel to the direction of metal flow (i.e. stress axis perpendicular to flow direction), or with the propagating crack running perpendicular to the direction of metal flow (i.e. stress axis parallel to the direction of metal flow). According to convention as it relates to rolled products, the fracture samples are hereafter designated as TF where the propagating crack runs in the direction of metal flow, and FT where the propagating crack runs perpendicular to the direction of metal flow. This is necessary because the current work has revealed that some alloy compositions prepared from the aforementioned HPDC plates display directionality of properties. Corresponding tensile samples are hereafter referred to as the T direction where the propagating crack in the tensile sample runs in the direction of metal flow, (i.e. corresponding to the TF fracture orientation) or the F direction where the propagating crack is perpendicular to the direction of metal flow. (i.e. corresponding to the FT fracture direction). As an example, the machined samples shown in
Table 4 shows tear test and tensile data of the same alloy X composition of the present invention, as in
Table 5 shows tear test and tensile data of the same alloy X of the present invention as in
From Tables 3, 4 and 5, it can be surmised that the two main factors influencing the fracture properties of the alloy are the composition and the choice of temper applied to the alloy. The levels of ductility present do not appear to strongly relate to the fracture properties, but do show some relationship where comparisons are made for the same temper condition.
Because of the differences between the two alloys examined in Table 3, further investigations of the microstructure were made as in
The change to the morphology of the Si plates in the as-cast condition as shown by
The microstructure with the alloy according to the present invention shown in
Since tensile ductility is not an optimal representation of fracture properties as indicated by the above examples, it is also desirable to develop alloys displaying both elevated levels of ductility and fracture toughness. Also, as indicated above, for the same temper condition, there is a rough correlation evident. In general, provided all conditions are constant and samples are the same, ductility of the alloy does allow for a rapid approximate determination of compositional ranges or limitations that may not be suited to high fracture resistant applications. In particular, limitations that arise due to alloy chemistry are important.
It can be seen from
Tables 6 to 8 show the chemistry of a range of alloys and their corresponding tensile properties in the as-cast, T4 and T6 conditions, respectively. For T4 conditions of Table 7 and T6 conditions of Table 8, solution treatment was conducted at 490° C. for 15 minutes followed by cold water quenching. T4 conditions were prepared by holding for 14 days at 25° C., and the T6 temper involved ageing for 24 h at 150° C. For alloy 3, in Tables 7 and 8, a solution treatment temperature of 480° C. was also tested, as noted in the table.
Table 6 reveals little difference in tensile ductility of the different alloys examined. A comparison of Alloy 1 and Alloy 3 shows only a minor change in ductility, which is raised from 4.1 to 6.1%, yet displays some reduction in 0.2% proof stress. Comparisons of Alloy 1 with Alloy 2, or Alloy 3 and Alloys 4, 5 and 6, shows that increasing the Mg content from ˜0.1 to ˜0.3wt % tends to increase 0.2% proof strength and slightly decrease ductility in the as-cast condition. In relation to Alloys 1 and 3, these correspond to the two alloys compared in Table 3.
A comparison of alloy 3 with alloy 7, shows that increasing Cu content also tends to decrease ductility. As for Alloy 1 and Alloy 2, or Alloy 3 and alloy 4, comparison of alloy 7 with alloy 8 also shows a reduced ductility with change in Mg content.
Table 7 shows that comparison of alloy 3 with alloy 1 shows a greater difference in ductility for the T4 condition compared to that present in Table 6. This is also consistent with the tear test results presented for the same two alloys in Table 3. Here the 0.2% proof stress and UTS is similar for both alloys. Similar trends to the as-cast results of Table 6 are noted in terms of Cu and Mg contents.
Table 8 shows that there is little difference in the respective ductility of alloy 3 and alloy 1 in the T6 condition. This result is consistent with that shown for the same two alloys in Table 7, and the tear test results presented in Table 3. Results shown in Table 8 confirm trends apparent in Table 6 in that increased Mg contents above 0.25% are preferably avoided, and that increased Cu content also produces some reduction in ductility.
From Tables 6 to 8, the upper limits on some elements may therefore be determined. For example, results from Alloy 6 suggest that Sr should preferably be omitted or minimized wherever possible. Mg contents are optimal when around 0.1%. Cu contents are optimal when below 3.5%, and are better as Cu levels reduce to below 3%. To ensure some heat treatment response is possible, Cu levels can be kept at above 1%. In the T4 and T6 treated conditions alloys 3 and 7 are preferred compared to the other alloys examined.
Although morphological alterations to the Si phase as shown in
In relation to the results of Tables 6 to 8, it is important to note the relationship of the alloy chemistries in reference to the present invention. Alloy 1 has a sludge factor of 1.18, but is outside of the limits of the current invention with regards to the Fe and Mn contents. Alloy 2 is similar to Alloy 1, having a sludge factor of 1.14, but is outside of the limits of the current invention in regards both to Fe and Mn contents and also the Mg content. Alloy 3 is inside the limits of the present invention, and has a sludge factor of 1.22. Alloy 4 has a sludge factor of 1.26 but is outside the limits of the current invention with regards to Mg content. Alloy 5 is similar to alloy 4, has a sludge factor of 1.22 and is outside the limits of the current invention with regard to Mg content. Alloy 6 is similar to alloy 5, has a sludge factor of 1.28 and is outside the limits of the current invention in regards to both the Mg and Sr contents. Alloy 7 is within the limits of the current invention and has a sludge factor of 1.6. Alloy 8 is outside the limits of the current invention in regards to Mg content and has a sludge factor of 1.46. Alloy 9 is similar to alloy 8, has a sludge factor of 1.23 and is outside of the limits of the current invention with regard to Mg content.
The preferred lower limits of Mg would ideally be 0.0% for alloys being heat treated, but some surprising results have also been found in this regard. Tables 9 to 11 show tensile results for a range of alloy compositions wherein the Mg, Cu, Zn and Ti contents were varied. All alloys in Tables 9 to 11 are within the scope of the current invention. For these alloys, it is surprising that for very low Mg contents of around 0.02%, no improvement to tensile properties are observed by heat treatment despite the presence of age hardening elements such as Cu. Additions of Zn appear to slightly decrease ductility, whereas additions of Ti appear to counteract this effect, slightly raising ductility. In the T4 tempers for all alloys, ductility is highest. The as-cast conditions for these alloys also display relatively high ductility. Although these alloys would be expected to exhibit excellent fracture resistance, the reduced strength would limit their potential applications.
Results shown for alloys 13 and 14 highlight the importance of optimizing the Mg content so as to gain a good hardening response, while maintaining adequate ductility. It is worth noting however, that even the alloys showing no age hardening response may find a range of applications where strength is less important than a high level of energy absorption.
To examine this further, samples of a different casting shape (tensile fatigue test bars) having a composition of Al-7.2Si-0.23Fe-1.8Cu-0.49Mn-0.07Mg-0.43Zn-0.05Ti-(<0.2 other total) were tested and were found to also display a good age hardening response by heat treatment, displaying elevated T6 tensile properties and high ductility.
Therefore, Mg contents for heat treated conditions of the alloy of the invention are ideally above 0.03% and less than 0.26%, and preferably in the range of 0.05 to 0.15 to ensure a good response of the alloy to heat treatment without causing any significant decrease in ductility.
Tables 12 to 14 show results for a range of 11 alloys in which the Mg content was raised progressively from 0.005 Mg to 0.22 in progressive increments. All alloys were within the scope of the present invention. As before, five tensile tests were conducted for each alloy in each condition examined. Table 12 shows results for the as-cast condition, Table 13 results for the T4 condition and Table 14 results for the T6 condition. Table 12 shows there is little variation in the tensile properties in the as-cast condition for the 11 alloys examined. Table 13 shows that for the T4 temper, the results are quite different. Alloys 15 and 16 do not show any advantage to tensile yield stress (0.2% proof stress) compared to the as-cast condition, but the tensile ductility is approximately doubled. Alloys 17 to 25 all show improvement to the yield stress (0.2% proof stress) compared to the as-cast condition as well as high levels of ductility, where the Mg content is above 0.05wt % Mg. Alloys 18 to 23 all display similar levels of ductility, and alloys 24 to 25 show lowered levels of ductility.
Table 14 shows that as for Table 13, there is effectively no response to heat treatment for alloys containing very low Mg levels (e.g. alloys 15 and 16.). Alloys 17 to 25 all display good levels of T6 treated tensile properties. Alloys 17 to 23 all display optimum tensile ductility while maintaining a good response to heat treatment.
Additionally, comparison of as-cast alloys as shown in Tables 9 and 12 gives an indication of the preferred limits of Si content. For Table 9, ductility ranges from 7.4 to 9.8%, where the Si levels were between 7 and 8%. For Table 12, the Si content is higher, of the order of 10 to 10.5 wt %, and the ductility values are lower at 4.2 to 5.3%.
Table 15 shows compositions for a range of seven alloys (alloys 26 to 32) within the scope of the present invention. Alloys 26 to 32 were used for determination of tear and tensile properties, (shown in Tables 16 to 19). The major changes were to the Cu content, which ranges from 1.82% Cu to 3.12% Cu in progressive increments. Table 16 shows results for the as-cast condition. Tables 17 to 19 respectively, show results for the T4 condition, the T6 condition, and for an underaged T6 condition (UA) and, in each case, the alloys were aged 6 h at 150° C. following solution treatment and quenching. All the T4, T6 and UA samples were solution treated at 480° C. before quenching. As before, five tensile test specimens and five tear test specimens were prepared for each alloy in each condition examined.
Tensile results shown in Table 16 for samples machined from plates and tested in the T direction for alloys 26 to 32 show that the 0.2% proof stress increases moderately with Cu content in the as-cast condition, while tensile elongation does not change appreciably across the compositions examined. The tear strength from plates tested in the TF direction also does not change appreciably across the seven alloys tested, although the Unit Propagation Energy does decrease as Cu content is raised. Similarly, the values of the Tear-to Yield-Stress ratio decrease from 1.73 for Alloys 26 and 27, down to 1.54 for Alloy 32.
Table 17 shows results as for Table 16, but for material treated to a T4 temper for samples machined from plates and tested in the T direction (tensile) or TF direction (tear) for alloys 26 to 32. In this case, the 0.2% proof stress increases more significantly with Cu content, from a lower value of 150 MPa for Alloy 26 up to a higher level of 196 MPa for Alloy 32. The tear strength increases from 305 MPa to 343 MPa with increasing Cu content for alloys 27 to 30, before then decreasing to a lower level of 317 MPa for Alloy 31. It is then little changed with a further addition of Cu, increasing only to 321 MPa for Alloy 32. The values for UPE change more significantly with the differences in Cu level, changing from 54.63 KJ/m2 for Alloy 26, and down to 34.5 KJ/m2 for Alloy 32. The tear-to-yield-ratio decreases from an upper level of 2.05 for Alloy 26 down to a lower level of 1.64 for Alloy 32.
Table 18 shows results as for Table 16 and 17, but now for material treated to a T6 temper for samples machined from plates and tested in the T direction (tensile) or TF direction (tear) for alloys 26 to 32. Here, the 0.2% proof stress rises with increases in Cu content from 217 MPa for Alloy 26 up to 304 MPa for Alloy 32. The tear strength is above 300 MPa for Alloys 26 to 30, and then falls below 300 MPa for Alloys 31 and 32. The values of UPE decrease monotonically with increasing Cu content, from 29.45 KJ/m2 for alloy 26 down to 9.72 KJ/m2 for Alloy 32. Similarly, the tear-to-yield-ratio is again at its highest for Alloy 26 at 1.45, before then falling to below a value of 1 for Alloys 31 and 32.
Table 19 shows results as for Tables 16 to 18, but now for material treated to an underaged T6 temper for samples machined from plates and tested in the T direction (tensile) or TF direction (tear) for alloys 26 to 32. Here, tensile results are rather similar to the results for the T4 temper shown in Table 17 despite the difference in the heat treatment procedure. in that the T4 treated material is held at 25° C. for 14 days, whereas the UA treated material is held 6 h at 150° C. Tear strength values are all above 300 MPa for the UA treated material. The values of UPE decrease monotonically with increases in Cu content, similar to the T4 treated alloy shown in Table 17. The tear-to-yield ratio is again highest for alloy 26 at 1.95, and decreases to a lower value of 1.49 for alloy 32.
Table 20 shows compositions for a range of additional different alloys (alloys 33 to 36) within the scope of the present invention, which were used for determination of tear and tensile properties.
Table 21 shows tear and tensile test results for alloy 33 and corresponds similarly to the composition used for tensile results shown for alloy 10 in Tables 9 to 11, being made from the same base ingot material. Five tensile samples and five tear test samples were tested in each condition. Tensile testing was in the T direction and tear testing in the TF direction. As is the case for this composition as shown in Tables 9 to 11, the alloy displays little or no heat treatment response in regards to its yield stress. However, heat treatment displays significant and substantial advantages to the fracture resistance of this alloy. The tear strength of this alloy is little changed with heat treatment, but the energy absorbed during fracture, particularly in the UPE, is greatly improved. Additionally, there is less difference between the UPE of the T4, T6 and UA tempers, which results because the alloy does not display a noticeable heat treatment response. The initiation energy of the heat treated conditions is also substantially better than the as-cast condition, because the material yields more before crack initiation, despite the presence of the sharp notch present for the tear test samples. The tear-to-yield ratio is very high for all conditions, but particularly so for the T4 and UA material where this value is over 2.5.
Table 22 shows tear and tensile test results for alloy 34, which is similar to alloy 26 from Table 15. Five tensile samples and five tear test samples were tested in each condition. Tensile testing was in the T direction and tear testing in the TF direction. In the T4 temper the alloy display similar levels of 0.2% proof stress and UTS as for the as-cast condition, but the elongation at failure is substantially increased from 4.9% to 9%. For the T6 temper, the 0.2% proof stress is raised to
216 MPa, while the UTS changes only marginally to 309 MPa. The elongation at failure is reduced compared to the T4 temper at 4.5%. Values of tear strength for alloy 34 are relatively high in all tempers examined, being consistent with the data for alloy 26 in Tables 16 to 18. The tear strength is however superior for alloy 34 in the T6 temper, compared to alloy 26 in the T6 temper. The tear-to-yield ratio is also similar between alloys 26 and 34 for the respective equivalent tempers. Values of UPE are also superior in all tempers examined for alloy 34 compared to alloy 26.
Table 23 shows tear and tensile test results for alloy 35. Alloy 35 is similar to alloy 34 except that the level of Mg was slightly increased, and the level of Cu slightly decreased. Five tensile samples and five tear test samples were tested in each condition. Similar to alloy 34, there is only a small change in tensile 0.2% proof stress and UTS for alloy 35 in the T4 temper when compared to the as-cast condition. The elongation at failure is however improved compared to both of the other conditions examined. Tensile testing was in the T direction and tear testing in the TF direction. The heat treatment response in the T6 temper for alloy 35 is again good. There is little difference between the tear strength of alloys 34 and 35 in their respective tempers, however in the T4 and T6 tempers the tear-to-yield ratio is reduced for alloy 35. Similarly, the values of UPE are also slightly reduced for alloy 35 compared to alloy 34. The overall fracture resistance of alloy 35 is slightly less than that of alloy 34.
Table 24 shows tear and tensile test results for alloy 36. Alloy 36 is similar to alloy 35 except that the level of Mg was again slightly increased, and the level of Cu again slightly decreased. Five tensile samples and five tear test samples were tested in each condition. The levels of tensile properties developed in alloy 36 are again similar to those for alloys 34 and 35 in as-cast and T4 tempers, although there is a slight increase across the three alloys as the levels
of Mg are raised. Similarly, the levels of tensile 0.2% proof stress are raised slightly across the three alloy compositions, in line with the increasing Mg content. Levels of TYR are again slightly decreased at this higher Mg content. The major difference for alloy 36 appears in the UPE values for the T6 temper, where the energy absorbed during crack propagation is more significantly reduced, despite the similar levels of tensile properties. This would tend to suggest that at a level of 0.23% Mg, that the fracture resistance is approaching its upper preferred limit.
In the examples above, upper and lower limits on key alloying elements are detailed for the alloys of the invention.
Finally, it is to be understood that various alterations, modifications and/or additions may be introduced into the constructions and arrangements of parts previously described without departing from the spirit or ambit of the invention.
Number | Date | Country | Kind |
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2008902123 | Apr 2008 | AU | national |
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/AU2009/000532 | 4/30/2009 | WO | 00 | 1/13/2011 |