CA2137135A1 - Brass alloy - Google Patents
Brass alloyInfo
- Publication number
- CA2137135A1 CA2137135A1 CA 2137135 CA2137135A CA2137135A1 CA 2137135 A1 CA2137135 A1 CA 2137135A1 CA 2137135 CA2137135 CA 2137135 CA 2137135 A CA2137135 A CA 2137135A CA 2137135 A1 CA2137135 A1 CA 2137135A1
- Authority
- CA
- Canada
- Prior art keywords
- alloy
- lead
- alloys
- remainder
- brass
- 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.)
- Abandoned
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C9/00—Alloys based on copper
- C22C9/04—Alloys based on copper with zinc as the next major constituent
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Domestic Plumbing Installations (AREA)
- Manufacture Of Metal Powder And Suspensions Thereof (AREA)
- Motor Or Generator Current Collectors (AREA)
- Conductive Materials (AREA)
Abstract
Described is a copper-based alloy containing 57 to 65 %
by wt. of copper, up to 3 % by wt. of other alloying constituents and bismuth as a machining additive, the remainder being zinc.
by wt. of copper, up to 3 % by wt. of other alloying constituents and bismuth as a machining additive, the remainder being zinc.
Description
Z1371~5 WO 93/24670 PC~/DE93/00468 DESCRIPTION
BRASS ALLOY
The invention relates to an alloy on a copper base with zinc as alloying constituent having the next to the highest share in the alloy. Such alloys, generally called brass, are used for the production of very different technical devices and components. Depending on the application, different alloying constituents are added to the brass alloys in order to obtain very specific properties which correspond to the respective intended use. If, for example, alloys are to be provided that are suitable for machining, the element lead is usually added to them in amounts of approximately 1 to 3 wt %. The lead has the effect that the chips occurring during machining are short-brittle. This characteristic is indispensable, particularly for the machining of workpieces on automatic machines.
When such lead-containing alloys are used for the production of components for the drinking water supply, there is the risk that the alloying constituent lead passes into - -the drinking water. Together with the drinking water, the lead reaches the human organism via the gastrointestinal tract, is mainly accumulated in the bones and leads to the known damage. Hazards due to lead are, however, also present in companies that produce lead-containing brass by melting or process products made from it. Here, the lead may enter the body through ingestion, inhalation or skin resorption.
It is known from DE 38 34 460 C2 to use an alloy for the production of components for water supply installations containing 1.5 to 7 wt ~ bismuth, 5 to 15 wt % zinc, 1 to 12 wt % tin and copper as remainder with accidental impurities.
This is a red cast alloy, which means, a tin bronze with zinc as additional alloying constituent. The disadvantage of such alloys is that they have a very wide solidification range because of the formation of a mixed substitution crystal between copper and zinc. This is a considerable disadvantage in that these alloys are only marginally suited for chill casting. This is mainly due to the fact that they have a relatively high melting temperature. The result of this is that, already after a few casting cycles, the chill molds become unusable owing to the high thermal stress.
Furthermore, these alloys have a comparatively wide - -solidification range of approximately 150 C. Together with the relatively high cooling rates in chill casting, this leads to an increased hot shortness of the cast parts.
Therefore, the alloys mentioned above can virtually only be used for sand casting processes.
A further disadvantage of the known alloy is the fact that a relatively high bismuth portion is required to make machining possible.
On this basis, it is the object of the invention to provide an alloy that is low in lead content or that is lead-free and suitable for the production of components for drinking water installations, which does not have the above disadvantages. The alloy should continue to have the casting and mechanical properties necessary for the intended use.
Water fittings, for example, should have a polishable surface and a pressure-tightness that is sufficient for the pressure ranges prevailing in drinking water supply systems, properties that depend directly on the fine-grainedness of the structure of the cast parts.
This object is solved by the characterizing features of claim 1. Surprisingly, it turned out that an alloy whose Cu content is set to 57 - 65 wt % and whose further alloying - -constituents do not exceed 3 wt % can be cast into the chill mold without any problems and, additionally, solidifies from the melt relatively finely grained and thus virtually free of shrinkholes. The latter is particularly advantageous in cases where the alloy is used to cast molded parts that should have a smooth and polishable surface, as is the case with high-quality fittings for kitchen and plumbing uses.
Furthermore, the fittings made with the alloy according to the invention are provided with a very good pressure-tightness which is due to the absence of shrinkholes or "sponge-like" regions in inner walls or sealing surfaces that separate different pressure zones. Sponge-like regions are understood to mean structural regions having a broken up, cavity-containing structure similar to a sponge. A further advantage of the invention is the fact that it is provided with good flow properties which is particularly important for the production of molded parts with a complex design.
If lead, which has been used so far as alloying constituent, is replaced by bismuth, the components produced with the alloy according to the invention can practically be classified as toxicologically safe. A cumulative toxic effect corresponding to that of lead is not known for - -bismuth. According to the DABl, bismuth is considerably 1 Translator's Note: DAB = Deutsches Arzneibuch = German Dispensatory.
` 2137~3S
less toxic than lead so that, in comparison, the concentrations caused by the passage of bismuth into the drinking water should lead to only a very minor potential health hazard. As could be shown with microorganisms and small animals, the toxic effect of bismuth on these organisms is approximately 10 times smaller than that of lead. Another indicator for the relative non-toxicity of bismuth can be seen in the fact that bismuth was classified as not hazardous to health in the German Regulation on Hazardous Materials and, contrary to lead, bismuth is not mentioned in standard regulations such as the TV02.
During the production of the alloy according to the invention, minor lead contaminations may possibly occur depending on the degree of purity of the alloying lS constituents used. Normally, however, these only amount to levels of approximately 0.3 wt % at most and are therefore rather negligible compared to the lead additives deliberately added to lead-containing brass alloys.
The dependent claims 2 and 3 list advantageous - -compositions of an alloy according to the invention. Here, 2 Translator's Note: TV0 = Trinkwasserverordnung =
Drinking Water Regulation.
--S--~ 1 3 ~
~O 93/24670 PCT/DE93/00468 it should be emphasized in particular that an addition of boron in an amount of 5 to 15 ppm can reduce the mean grain size of the structure.
The advantage of the alloys according to claims 4 and 5 is that they are dezincification-resistant. Because of this characteristic, drinking water fittings, for example, made from these alloys can also be used in areas with high water aggressivity and they have a generally higher service life.
In order to arrive at dezincification-resistant brass alloys when starting from conventional brass alloys, such as Ms 60 Fk tsic~, it is necessary to increase the Cu content, for example, to 64%. Such alloys, however, are not suitable for many applications, specifically for the manufacture of fittings for sanitary installations, because their structure is too coarse, which brings about the known negative concomitant phenomena such as increased formation of shrinkholes. Up until now, efforts have failed to refine the grain of brass alloys having an increased Cu content by means of boron which is normally used for these purposes.
io Therefore, virtually only the known, not dezincification-resistant alloys were used for the application mentioned.
It turned out, surprisingly, that grain refining with 21371~
boron is possible in spite of a Cu content that is increased compared to the known alloys, if the elements Mn, Si and Sb are added by alloying in amounts according to the invention and if, simultaneously, the Fe content can be limited to a maximum of 0.25 wt %. Furthermore, it turned out, surprisingly, that the alloy is provided with enhanced hot shortness if the Sn content is as low as possible but, at least, does not exceed 0.25 wt %. A further advantage is that the occurrence of hard inclusions is strongly repressed.
Hard inclusions, which are mainly disturbing during surface finishing, mainly occur in increased numbers in conventional lead-containing brass alloys if these have been refined with boron.
In the following, the invention is explained in greater detail by way of embodiments:
ExamPle 1:
By melting together the corresponding alloying constituents, a melt was obtained containing 59.78 wt % Cu, 0.60 wt % Al, 1.00 wt % Bi, 13 ppm B, as melting-related contaminations 0.02 wt % Pb, 0.01 wt % Sn, 0.02 wt % Fe, 0.01 wt % Sb and Zn as remainder. The melt was cast to form sample ingots and finished cast parts (fittings). Different 2137~3~
~.
~O 93/24670 PCT/DE93/00468 standard tests were carried out with parts of the ingots or with the finished parts:
In order to test the polishability of the alloy according to the invention a number of polishing tests were carried out. The result of this test series was that the formed parts produced with the alloy according to the invention are provided with the surface polishability required for high-quality fittings. Fracture tests were also conducted with all sample pieces. Here, it was found that there were practically no foreign inclusions or "sponge regions." Particularly the latter are often the reason for leakage if they are disposed in the separation walls between spaces with different pressurization or, for instance, in seats for seals.
The structure of the examined samples was essentially globulitic throughout and had a mean grain size of approximately 30 ~m. The casting spiral flow length (according to Schneider) at a temperature of 1,000 C to 1,005~ C was designated as the measure for the flowability of-the alloy. The determined values were between 522 mm and 531 mm and thus within the range of the values known from Gk Ms 60 Fk (500 mm - 600 mm).
~ 213713~ -Several finished parts were subjected to machining on automatic machines by producing threads and sealing end faces, as is done in the normal production process. It turned out that the molded parts cast with the alloy according to the invention could be machined just as well as those made from the conventional brass alloy Gk Ms 60 Fk.
The chips that were machined off of the molded parts were short-brittle, as is the case with lead-containing brass alloys.
Also in grinding tests in which the material removal during a predetermined time was determined, no significant differences compared to the conventional brass were found.
With regard to the electroplating ability of the castings made from the alloy according to the invention there were also no differences found compared to conventional brass castings.
The mechanical properties were determined pursuant to DIN 1709, paragraph 5. From the wedge test specimens cast in conformity with standards, the lowest section was taken for ~0 the "round test specimen." The round test specimens were produced and drawn according to DIN 50150. The values that were determined are listed in the following table:
~137i35 Table 1:
Alloy Gk Ms60 Fk acc. to invention Elongation limit Rp 0.2 (N/mm2): 157.0 153.7 Tensile strength Rm (N/mm2): 360.8 396 Elongation at rupture A10 (%): 12.6 19.7 Brinell hardness 2.5/62.5 (HB): 121 107 For the determination of the dezincification resistance, a dezincification sample was produced pursuant to the IS0 Standard 6509-1981 (E). The dezincification test itself was carried out according to the Australian Standard No. 2345-1980. The dezincification depths found were greater than 100 ~m throughout but were within the ranges known from Gk Ms 60 Fk.
Example 2:
This embodiment concerns an alloy of the following composition (wt %): -Cu: 63.00%, Bi: 0.8%, Mn: 0.45%, Si: 0.5%, Al: 0.5%, Sb:
0.1%, B: 10 ppm, Pb: <0.10%, Sn: <0.10%, Fe: <0.10%, Ni:
<0.10%, Zn: remainder.
~O 93/24670 PCT/DE93/00468 For the determination of the dezincification resistance, transverse sections were cold-separated from the plumbing fittings made from the alloy according to the invention (sample P III in Table 2) and subjected to a test pursuant to IS0 6509 (Corrosion of metals and alloys/Determination of dezincification resistance of brass-, edition 1981)3. The casting temperature was 1,000 C. For purposes of comparison, 2 samples (PI and PII) with the following known composition were tested (data in wt %):
Cu: 60.06%, Zn: 37.38%, Ni: 0.030%, Al: 0.65%, Mn:
<0.010%, Sn: 0.10%, Sb: 0.020%, Si: 0.010%, Fe: 0.080%, Pb:
1.65%, B: 0.0008%.
The result of the dezincification resistance test is shown in the following Table 14:
Table 2:
SampleDezincification depth (~m) 3 Translator's Note: Text in brackets up to "brass-"
appears in English in German original text.
BRASS ALLOY
The invention relates to an alloy on a copper base with zinc as alloying constituent having the next to the highest share in the alloy. Such alloys, generally called brass, are used for the production of very different technical devices and components. Depending on the application, different alloying constituents are added to the brass alloys in order to obtain very specific properties which correspond to the respective intended use. If, for example, alloys are to be provided that are suitable for machining, the element lead is usually added to them in amounts of approximately 1 to 3 wt %. The lead has the effect that the chips occurring during machining are short-brittle. This characteristic is indispensable, particularly for the machining of workpieces on automatic machines.
When such lead-containing alloys are used for the production of components for the drinking water supply, there is the risk that the alloying constituent lead passes into - -the drinking water. Together with the drinking water, the lead reaches the human organism via the gastrointestinal tract, is mainly accumulated in the bones and leads to the known damage. Hazards due to lead are, however, also present in companies that produce lead-containing brass by melting or process products made from it. Here, the lead may enter the body through ingestion, inhalation or skin resorption.
It is known from DE 38 34 460 C2 to use an alloy for the production of components for water supply installations containing 1.5 to 7 wt ~ bismuth, 5 to 15 wt % zinc, 1 to 12 wt % tin and copper as remainder with accidental impurities.
This is a red cast alloy, which means, a tin bronze with zinc as additional alloying constituent. The disadvantage of such alloys is that they have a very wide solidification range because of the formation of a mixed substitution crystal between copper and zinc. This is a considerable disadvantage in that these alloys are only marginally suited for chill casting. This is mainly due to the fact that they have a relatively high melting temperature. The result of this is that, already after a few casting cycles, the chill molds become unusable owing to the high thermal stress.
Furthermore, these alloys have a comparatively wide - -solidification range of approximately 150 C. Together with the relatively high cooling rates in chill casting, this leads to an increased hot shortness of the cast parts.
Therefore, the alloys mentioned above can virtually only be used for sand casting processes.
A further disadvantage of the known alloy is the fact that a relatively high bismuth portion is required to make machining possible.
On this basis, it is the object of the invention to provide an alloy that is low in lead content or that is lead-free and suitable for the production of components for drinking water installations, which does not have the above disadvantages. The alloy should continue to have the casting and mechanical properties necessary for the intended use.
Water fittings, for example, should have a polishable surface and a pressure-tightness that is sufficient for the pressure ranges prevailing in drinking water supply systems, properties that depend directly on the fine-grainedness of the structure of the cast parts.
This object is solved by the characterizing features of claim 1. Surprisingly, it turned out that an alloy whose Cu content is set to 57 - 65 wt % and whose further alloying - -constituents do not exceed 3 wt % can be cast into the chill mold without any problems and, additionally, solidifies from the melt relatively finely grained and thus virtually free of shrinkholes. The latter is particularly advantageous in cases where the alloy is used to cast molded parts that should have a smooth and polishable surface, as is the case with high-quality fittings for kitchen and plumbing uses.
Furthermore, the fittings made with the alloy according to the invention are provided with a very good pressure-tightness which is due to the absence of shrinkholes or "sponge-like" regions in inner walls or sealing surfaces that separate different pressure zones. Sponge-like regions are understood to mean structural regions having a broken up, cavity-containing structure similar to a sponge. A further advantage of the invention is the fact that it is provided with good flow properties which is particularly important for the production of molded parts with a complex design.
If lead, which has been used so far as alloying constituent, is replaced by bismuth, the components produced with the alloy according to the invention can practically be classified as toxicologically safe. A cumulative toxic effect corresponding to that of lead is not known for - -bismuth. According to the DABl, bismuth is considerably 1 Translator's Note: DAB = Deutsches Arzneibuch = German Dispensatory.
` 2137~3S
less toxic than lead so that, in comparison, the concentrations caused by the passage of bismuth into the drinking water should lead to only a very minor potential health hazard. As could be shown with microorganisms and small animals, the toxic effect of bismuth on these organisms is approximately 10 times smaller than that of lead. Another indicator for the relative non-toxicity of bismuth can be seen in the fact that bismuth was classified as not hazardous to health in the German Regulation on Hazardous Materials and, contrary to lead, bismuth is not mentioned in standard regulations such as the TV02.
During the production of the alloy according to the invention, minor lead contaminations may possibly occur depending on the degree of purity of the alloying lS constituents used. Normally, however, these only amount to levels of approximately 0.3 wt % at most and are therefore rather negligible compared to the lead additives deliberately added to lead-containing brass alloys.
The dependent claims 2 and 3 list advantageous - -compositions of an alloy according to the invention. Here, 2 Translator's Note: TV0 = Trinkwasserverordnung =
Drinking Water Regulation.
--S--~ 1 3 ~
~O 93/24670 PCT/DE93/00468 it should be emphasized in particular that an addition of boron in an amount of 5 to 15 ppm can reduce the mean grain size of the structure.
The advantage of the alloys according to claims 4 and 5 is that they are dezincification-resistant. Because of this characteristic, drinking water fittings, for example, made from these alloys can also be used in areas with high water aggressivity and they have a generally higher service life.
In order to arrive at dezincification-resistant brass alloys when starting from conventional brass alloys, such as Ms 60 Fk tsic~, it is necessary to increase the Cu content, for example, to 64%. Such alloys, however, are not suitable for many applications, specifically for the manufacture of fittings for sanitary installations, because their structure is too coarse, which brings about the known negative concomitant phenomena such as increased formation of shrinkholes. Up until now, efforts have failed to refine the grain of brass alloys having an increased Cu content by means of boron which is normally used for these purposes.
io Therefore, virtually only the known, not dezincification-resistant alloys were used for the application mentioned.
It turned out, surprisingly, that grain refining with 21371~
boron is possible in spite of a Cu content that is increased compared to the known alloys, if the elements Mn, Si and Sb are added by alloying in amounts according to the invention and if, simultaneously, the Fe content can be limited to a maximum of 0.25 wt %. Furthermore, it turned out, surprisingly, that the alloy is provided with enhanced hot shortness if the Sn content is as low as possible but, at least, does not exceed 0.25 wt %. A further advantage is that the occurrence of hard inclusions is strongly repressed.
Hard inclusions, which are mainly disturbing during surface finishing, mainly occur in increased numbers in conventional lead-containing brass alloys if these have been refined with boron.
In the following, the invention is explained in greater detail by way of embodiments:
ExamPle 1:
By melting together the corresponding alloying constituents, a melt was obtained containing 59.78 wt % Cu, 0.60 wt % Al, 1.00 wt % Bi, 13 ppm B, as melting-related contaminations 0.02 wt % Pb, 0.01 wt % Sn, 0.02 wt % Fe, 0.01 wt % Sb and Zn as remainder. The melt was cast to form sample ingots and finished cast parts (fittings). Different 2137~3~
~.
~O 93/24670 PCT/DE93/00468 standard tests were carried out with parts of the ingots or with the finished parts:
In order to test the polishability of the alloy according to the invention a number of polishing tests were carried out. The result of this test series was that the formed parts produced with the alloy according to the invention are provided with the surface polishability required for high-quality fittings. Fracture tests were also conducted with all sample pieces. Here, it was found that there were practically no foreign inclusions or "sponge regions." Particularly the latter are often the reason for leakage if they are disposed in the separation walls between spaces with different pressurization or, for instance, in seats for seals.
The structure of the examined samples was essentially globulitic throughout and had a mean grain size of approximately 30 ~m. The casting spiral flow length (according to Schneider) at a temperature of 1,000 C to 1,005~ C was designated as the measure for the flowability of-the alloy. The determined values were between 522 mm and 531 mm and thus within the range of the values known from Gk Ms 60 Fk (500 mm - 600 mm).
~ 213713~ -Several finished parts were subjected to machining on automatic machines by producing threads and sealing end faces, as is done in the normal production process. It turned out that the molded parts cast with the alloy according to the invention could be machined just as well as those made from the conventional brass alloy Gk Ms 60 Fk.
The chips that were machined off of the molded parts were short-brittle, as is the case with lead-containing brass alloys.
Also in grinding tests in which the material removal during a predetermined time was determined, no significant differences compared to the conventional brass were found.
With regard to the electroplating ability of the castings made from the alloy according to the invention there were also no differences found compared to conventional brass castings.
The mechanical properties were determined pursuant to DIN 1709, paragraph 5. From the wedge test specimens cast in conformity with standards, the lowest section was taken for ~0 the "round test specimen." The round test specimens were produced and drawn according to DIN 50150. The values that were determined are listed in the following table:
~137i35 Table 1:
Alloy Gk Ms60 Fk acc. to invention Elongation limit Rp 0.2 (N/mm2): 157.0 153.7 Tensile strength Rm (N/mm2): 360.8 396 Elongation at rupture A10 (%): 12.6 19.7 Brinell hardness 2.5/62.5 (HB): 121 107 For the determination of the dezincification resistance, a dezincification sample was produced pursuant to the IS0 Standard 6509-1981 (E). The dezincification test itself was carried out according to the Australian Standard No. 2345-1980. The dezincification depths found were greater than 100 ~m throughout but were within the ranges known from Gk Ms 60 Fk.
Example 2:
This embodiment concerns an alloy of the following composition (wt %): -Cu: 63.00%, Bi: 0.8%, Mn: 0.45%, Si: 0.5%, Al: 0.5%, Sb:
0.1%, B: 10 ppm, Pb: <0.10%, Sn: <0.10%, Fe: <0.10%, Ni:
<0.10%, Zn: remainder.
~O 93/24670 PCT/DE93/00468 For the determination of the dezincification resistance, transverse sections were cold-separated from the plumbing fittings made from the alloy according to the invention (sample P III in Table 2) and subjected to a test pursuant to IS0 6509 (Corrosion of metals and alloys/Determination of dezincification resistance of brass-, edition 1981)3. The casting temperature was 1,000 C. For purposes of comparison, 2 samples (PI and PII) with the following known composition were tested (data in wt %):
Cu: 60.06%, Zn: 37.38%, Ni: 0.030%, Al: 0.65%, Mn:
<0.010%, Sn: 0.10%, Sb: 0.020%, Si: 0.010%, Fe: 0.080%, Pb:
1.65%, B: 0.0008%.
The result of the dezincification resistance test is shown in the following Table 14:
Table 2:
SampleDezincification depth (~m) 3 Translator's Note: Text in brackets up to "brass-"
appears in English in German original text.
4 Translator's Note: "1" appears in German original text.
~13713~
In sample III, a dezincification depth of 60 ~m was found, while the samples consisting of conventional Gk Ms 60 Fk had considerably greater dezincification depths.
According to the standards BS 2872 (BS = British Standard), BS 2974, SS 11710 (SS = Swedish Standard) or the Swedish Construction Standard R8, the sample PIII is dezincification-resistant. The allowable dezincification depth for castings is 100 ~m according to BS, 200 ~m according to the Swedish Construction Standard R8.
The tests described in the following were carried out with samples PIV and PV having the following compositions (data in wt %~:
PIV: Cu: 64.81%, Bi: 0.33%, Mn: 0.44%, Fe: 0.039%, B:
0.0015%, Ni: <0.01%, Si: 0.53%, Sn: <0.01%, Pb:
<0.01%, Al: 0.53%, Zn: remainder.
PV: Cu: 64.83%, Bi: 0.53%, Fe: 0.049%, Mn: 0.40%. The remaining alloying constituents correspond to those of PIV.
First, the castings were cast under the usual production 2`0 conditions. These castings were first subjected to a cylindrical machine grinding, a manual finish grinding and fine grinding and, finally, to a machine as well as manual 2~3713~ -polishing. In this process, the parts were channeled into the normal production and they were weighed in the raw state and after each of the mentioned operations. Here, it was found that, compared to castings made from conventional brass Gk Ms 60 Fk, the material removed through the machine grinding was significantly less. The surface quality of the parts made from the alloy according to the invention was better compared to that of conventional castings, which could be seen from a lower number of complaints after the first grinding or polishing operation. The above-mentioned samples PIV and PV were also subjected to fracture tests in order to examine their structure for shrinkholes and "sponge regions."
All samples were free of such structural flaws.
The microstructure of the alloy corresponding to PIV and PV was determined with usual metallographic methods. The structure showed an essentially globulitic grain structure with a mean grain size of approximately 35 ~m. The maximum grain size was below 100 ~m.
For the determination of machinability, 60 castings (fittings) were machined on automatic machines. Sealing end faces and threads, for example, were produced. It was found that the machinability can take place without a considerable -change of the machining parameters that are normal for conventional castings.
The mechanical parameters elongation limit, tensile strength, elongation at rupture and Brinell hardness were determined according to the usual standardized methods. The result of these series of tests was that the cited mechanical values were comparable to those of the known brass alloy Gk Ms 60 Fk.
~13713~
In sample III, a dezincification depth of 60 ~m was found, while the samples consisting of conventional Gk Ms 60 Fk had considerably greater dezincification depths.
According to the standards BS 2872 (BS = British Standard), BS 2974, SS 11710 (SS = Swedish Standard) or the Swedish Construction Standard R8, the sample PIII is dezincification-resistant. The allowable dezincification depth for castings is 100 ~m according to BS, 200 ~m according to the Swedish Construction Standard R8.
The tests described in the following were carried out with samples PIV and PV having the following compositions (data in wt %~:
PIV: Cu: 64.81%, Bi: 0.33%, Mn: 0.44%, Fe: 0.039%, B:
0.0015%, Ni: <0.01%, Si: 0.53%, Sn: <0.01%, Pb:
<0.01%, Al: 0.53%, Zn: remainder.
PV: Cu: 64.83%, Bi: 0.53%, Fe: 0.049%, Mn: 0.40%. The remaining alloying constituents correspond to those of PIV.
First, the castings were cast under the usual production 2`0 conditions. These castings were first subjected to a cylindrical machine grinding, a manual finish grinding and fine grinding and, finally, to a machine as well as manual 2~3713~ -polishing. In this process, the parts were channeled into the normal production and they were weighed in the raw state and after each of the mentioned operations. Here, it was found that, compared to castings made from conventional brass Gk Ms 60 Fk, the material removed through the machine grinding was significantly less. The surface quality of the parts made from the alloy according to the invention was better compared to that of conventional castings, which could be seen from a lower number of complaints after the first grinding or polishing operation. The above-mentioned samples PIV and PV were also subjected to fracture tests in order to examine their structure for shrinkholes and "sponge regions."
All samples were free of such structural flaws.
The microstructure of the alloy corresponding to PIV and PV was determined with usual metallographic methods. The structure showed an essentially globulitic grain structure with a mean grain size of approximately 35 ~m. The maximum grain size was below 100 ~m.
For the determination of machinability, 60 castings (fittings) were machined on automatic machines. Sealing end faces and threads, for example, were produced. It was found that the machinability can take place without a considerable -change of the machining parameters that are normal for conventional castings.
The mechanical parameters elongation limit, tensile strength, elongation at rupture and Brinell hardness were determined according to the usual standardized methods. The result of these series of tests was that the cited mechanical values were comparable to those of the known brass alloy Gk Ms 60 Fk.
Claims (9)
1. Alloy with the following composition (wt %):
Cu: 57 - 65%
Bi: 0.3 - 1.5%
Al: 0.4 - 0.8%
B: 5 - 15 ppm Impurities: 0 - 1%
Zn as remainder.
Cu: 57 - 65%
Bi: 0.3 - 1.5%
Al: 0.4 - 0.8%
B: 5 - 15 ppm Impurities: 0 - 1%
Zn as remainder.
2. Alloy according to claim 1, characterized in that the composition is as follows (wt %):
Cu: 57 - 62%
Bi: 0.3 - 1.5%
Al: 0.4 - 0.8%
B: 5 - 15 ppm Impurities: 0 - 1%
Zn: Remainder
Cu: 57 - 62%
Bi: 0.3 - 1.5%
Al: 0.4 - 0.8%
B: 5 - 15 ppm Impurities: 0 - 1%
Zn: Remainder
3. Alloy according to claim 2, characterized in that the composition is as follows (wt %):
Cu: 59.78 Al: 0.60 Bi: 1.00 B: 13 ppm Pb: 0.02 Sn: 0.01 Fe: 0.02 Sb: 0.01 Si: 0. 01 Zn: Remainder
Cu: 59.78 Al: 0.60 Bi: 1.00 B: 13 ppm Pb: 0.02 Sn: 0.01 Fe: 0.02 Sb: 0.01 Si: 0. 01 Zn: Remainder
4. Alloy according to claim 1, characterized in that the composition is as follows (wt %):
Cu: 62 - 65%
Bi: 0.3 - 1.5%
Mn: 0.3 - 0.7%
Si: 0.3 - 0.7%
Al: 0.3 - 0.7%
Sb: 0.05 - 0.15%
B: 5 - 15 ppm Miscellaneous: <1%
Zn: Remainder
Cu: 62 - 65%
Bi: 0.3 - 1.5%
Mn: 0.3 - 0.7%
Si: 0.3 - 0.7%
Al: 0.3 - 0.7%
Sb: 0.05 - 0.15%
B: 5 - 15 ppm Miscellaneous: <1%
Zn: Remainder
5. Alloy according to claim 4, characterized in that the composition is as follows (wt %):
Cu: 62 - 65%
Bi: 0.5 - 1.5%
Mn: 0.3 - 0.5%
Si: 0.5 - 0.7%
Al: 0.3 - 0.7%
Sb: 0.05 - 0.1%
B: 5 - 15 ppm Pb: 0 - 0.3%
Sn: 0 - 0.25%
Fe: 0 - 0.20%
Ni: 0 - 0.5%
Zn: Remainder
Cu: 62 - 65%
Bi: 0.5 - 1.5%
Mn: 0.3 - 0.5%
Si: 0.5 - 0.7%
Al: 0.3 - 0.7%
Sb: 0.05 - 0.1%
B: 5 - 15 ppm Pb: 0 - 0.3%
Sn: 0 - 0.25%
Fe: 0 - 0.20%
Ni: 0 - 0.5%
Zn: Remainder
6. Alloy according to claim 5, characterized in that the composition is as follows (wt %):
Cu: 63.0%
Bi: 0.8%
Mn: 0.45%
si: 0. 5%
Al: 0.5%
Sb: 0.1%
B: 10 ppm Pb: <0.1%
Sn: <0.1%
Fe: <0.1%
Ni: <0.1%
Zn: Remainder
Cu: 63.0%
Bi: 0.8%
Mn: 0.45%
si: 0. 5%
Al: 0.5%
Sb: 0.1%
B: 10 ppm Pb: <0.1%
Sn: <0.1%
Fe: <0.1%
Ni: <0.1%
Zn: Remainder
7. Alloy according to claim 5, characterized in that the composition is as follows (wt %):
Cu: 64.81%
Bi: 0.33%
Mn: 0.44%
Fe: 0.039%
B: 15 ppm Ni: <0.01%
Si: 0.53%
Sn: <0.01%
Pb: <0.01%
Al: 0.53%
Zn: Remainder
Cu: 64.81%
Bi: 0.33%
Mn: 0.44%
Fe: 0.039%
B: 15 ppm Ni: <0.01%
Si: 0.53%
Sn: <0.01%
Pb: <0.01%
Al: 0.53%
Zn: Remainder
8. Alloy according to claim 5, characterized in that the composition is as follows (wt %):
Cu: 64.83%
Bi: 0.53%
Fe: 0.049%
Mn: 0.40%
B: 15 ppm Ni: <0.01%
Si: 0.53%
Sn: <0.01%
Pb: <0.01%
Al: 0.53%
Zn: Remainder
Cu: 64.83%
Bi: 0.53%
Fe: 0.049%
Mn: 0.40%
B: 15 ppm Ni: <0.01%
Si: 0.53%
Sn: <0.01%
Pb: <0.01%
Al: 0.53%
Zn: Remainder
9. Use of an alloy according to claims 1 through 8 for the production of components for drinking water installations.
Applications Claiming Priority (8)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEP4218513.0 | 1992-06-02 | ||
DE4218513 | 1992-06-02 | ||
DEP4240880.6 | 1992-12-04 | ||
DE4240880 | 1992-12-04 | ||
DEP4312484.4 | 1993-04-16 | ||
DEP4312466.6 | 1993-04-16 | ||
DE4312484 | 1993-04-16 | ||
DE4312466 | 1993-04-16 |
Publications (1)
Publication Number | Publication Date |
---|---|
CA2137135A1 true CA2137135A1 (en) | 1993-12-09 |
Family
ID=27435479
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA 2137135 Abandoned CA2137135A1 (en) | 1992-06-02 | 1993-05-28 | Brass alloy |
Country Status (10)
Country | Link |
---|---|
EP (1) | EP0642596B1 (en) |
JP (1) | JP2793041B2 (en) |
KR (1) | KR100191702B1 (en) |
AU (1) | AU669406B2 (en) |
BR (1) | BR9306475A (en) |
CA (1) | CA2137135A1 (en) |
DE (1) | DE59300867D1 (en) |
ES (1) | ES2082644T3 (en) |
HK (1) | HK107096A (en) |
WO (1) | WO1993024670A1 (en) |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ATE178362T1 (en) * | 1993-04-22 | 1999-04-15 | Federalloy Inc | SANITARY FACILITIES |
DE4438485C2 (en) * | 1994-10-28 | 1998-05-20 | Wieland Werke Ag | Use of a copper-zinc alloy for drinking water installations |
JP2003277855A (en) * | 2002-03-22 | 2003-10-02 | San-Etsu Metals Co Ltd | Lead-free, free-cutting brass alloy material and production method thereof |
JP4620963B2 (en) * | 2004-03-31 | 2011-01-26 | Dowaホールディングス株式会社 | Brass, manufacturing method thereof, and parts using the same |
WO2009047919A1 (en) * | 2007-10-10 | 2009-04-16 | Toto Ltd. | Lead-free free-cutting brass excelling in castability |
WO2009048008A1 (en) * | 2007-10-10 | 2009-04-16 | Toto Ltd. | Lead-free, free-machining brass having excellent castability |
JP5513230B2 (en) * | 2009-06-17 | 2014-06-04 | サンエツ金属株式会社 | Copper-base alloy for casting |
CN101876012B (en) * | 2009-12-09 | 2015-01-21 | 路达(厦门)工业有限公司 | Brass alloy with excellent stress corrosion resistance and manufacture method thereof |
TWI398532B (en) * | 2010-01-22 | 2013-06-11 | Modern Islands Co Ltd | Lead-free brass alloy |
WO2018076165A1 (en) * | 2016-10-25 | 2018-05-03 | 广东伟强铜业科技有限公司 | Free-cutting brass alloy and manufacturing method therefor |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE889984C (en) * | 1944-02-11 | 1953-09-14 | Wieland Werke Ag | Use of copper-zinc alloys for workpieces to be machined |
JPS54135618A (en) * | 1978-04-13 | 1979-10-22 | Sumitomo Metal Mining Co | Cuttable presssformable brass bismuth alloy |
GB8724311D0 (en) * | 1987-10-16 | 1987-11-18 | Imi Yorkshire Fittings | Fittings |
US5137685B1 (en) * | 1991-03-01 | 1995-09-26 | Olin Corp | Machinable copper alloys having reduced lead content |
US5288458A (en) * | 1991-03-01 | 1994-02-22 | Olin Corporation | Machinable copper alloys having reduced lead content |
-
1993
- 1993-05-28 KR KR1019940704212A patent/KR100191702B1/en not_active IP Right Cessation
- 1993-05-28 BR BR9306475A patent/BR9306475A/en not_active IP Right Cessation
- 1993-05-28 WO PCT/DE1993/000468 patent/WO1993024670A1/en active IP Right Grant
- 1993-05-28 EP EP93909801A patent/EP0642596B1/en not_active Expired - Lifetime
- 1993-05-28 CA CA 2137135 patent/CA2137135A1/en not_active Abandoned
- 1993-05-28 DE DE59300867T patent/DE59300867D1/en not_active Expired - Fee Related
- 1993-05-28 JP JP6500087A patent/JP2793041B2/en not_active Expired - Lifetime
- 1993-05-28 AU AU53404/94A patent/AU669406B2/en not_active Ceased
- 1993-05-28 ES ES93909801T patent/ES2082644T3/en not_active Expired - Lifetime
-
1996
- 1996-06-19 HK HK107096A patent/HK107096A/en not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
DE59300867D1 (en) | 1995-12-07 |
KR100191702B1 (en) | 1999-06-15 |
BR9306475A (en) | 1998-06-30 |
EP0642596A1 (en) | 1995-03-15 |
ES2082644T3 (en) | 1996-03-16 |
JPH08503520A (en) | 1996-04-16 |
WO1993024670A1 (en) | 1993-12-09 |
JP2793041B2 (en) | 1998-09-03 |
EP0642596B1 (en) | 1995-11-02 |
AU669406B2 (en) | 1996-06-06 |
HK107096A (en) | 1996-06-28 |
AU5340494A (en) | 1993-12-30 |
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