A BRAZING MATERIAL FOR BRAZING ARTICLES OF AUSTENITIC STAINLESS STEEL AND METHOD THEREFORE

Abstract

A brazing material for brazing articles of austenitic stainless steel comprises: 1.8-2.2% Molybdenum (Mo); 12.5-13.5% Nickel (Ni); 16.8-18.6% Chromium (Cr); 7.0-12.0% Silicon (Si); 3.0-5.5% Mn; 1.0-2.0% Boron (B); balance being Iron (Fe) and small amounts of other elements, wherein the percentages of these elements are lower than 0.1% for each element, all percentages being given by weight.

Claims

1. A brazing material, comprising: 1.6 to 2.6% Molybdenum (Mo); 12.5 to 14.5% Nickel (Ni); 18.0 to 20.0% Chromium (Cr); 6.8 to 8.2% Silicon (Si); 4.0 to 5.8% Mn; 0.6 to 1.2% Boron (B); balance being Iron (Fe) and small amounts of other elements, wherein the percentages of these elements are lower than 0.1% for each element, all percentages being given by weight.

2. The brazing material of claim 1, wherein the percentage of Molybdenum (Mo) is 1.9-2.2%.

3. The brazing material of claim 1, wherein the percentage of Nickel (Ni) is 13.2-13.7%.

4. The brazing material of claim 1, wherein the percentage of Chromium (Cr) is 18.0-19.0%.

5. The brazing material of claim 1, wherein the percentage of Silicon (Si) is 7.3-8.2%.

6. The brazing material of claim 1, wherein the percentage of Silicon (Si) is 7.8-8.2%.

7. The brazing material of claim 1, wherein the percentage of Manganese (Mn) is 4.5-5.5%.

8. The brazing material of claim 1, wherein the percentage of Manganese (Mn) is 5.0-5.5%.

9. The brazing material of claim 1, wherein the percentage of Manganese (Mn) is 5.1-5.5%.

10. The brazing material of claim 1, wherein the percentage of Manganese (Mn) is 5.2-5.4%.

11. The brazing material of claim 1, wherein the percentage of Boron (B) is 0.8-1.2%.

12. The brazing material of claim 1, wherein the percentage of Boron (B) is 1.0-1.2%.

13. The brazing material of claim 1, wherein the percentage of Boron (B) is 1.0-1.1%.

14. Use of a brazing material according to claim 1 for brazing together articles of stainless steel.

15. The use according to claim 14, wherein the stainless steel is an austenitic stainless steel of type 304 or 316.

16. Use according to any of the claim 14, wherein the stainless steel articles to be brazed are heat exchanger plates.

17. A heat exchanger made from plates from stainless steel according to claim 15.

18. The heat exchanger made from plates from stainless steel being brazed with a brazing material according to claim 1.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0036] In the following, the invention will be described by reference to preferred embodiments of the invention, in conjunction with the accompanying drawings, wherein:

[0037] FIG. 1a is a graph showing DTA-TGA curves for several different brazing materials according to the present invention;

[0038] FIG. 1b is a graph showing a DTA-TGA diagram for one brazing material having a composition according to the present invention;

[0039] FIG. 2 is three graphs showing the main effects for erosion as a function of percentage of Silicon, Manganese and Boron; and

[0040] FIG. 3 is a scatterplot showing erosion vs. brazing temperature minus liquidus temperature, i.e. superheat, for different brazing materials.

DESCRIPTION OF EMBODIMENTS

[0041] The brazing material according to the invention contains: [0042] 1.6-2.6% Molybdenum (Mo); [0043] 12.5-14.5% Nickel (Ni); [0044] 18-20% Chromium (Cr); [0045] 6.8-8.2% Silicon (Si); [0046] 3.0-6.4% Manganese (Mn); [0047] 0.6-1.2% Boron (B);

[0048] Balance being Iron (Fe) and small amounts of other elements, wherein the percentages of these elements are lower than 0.1% for each element, all percentages being given by weight.

[0049] Below, some reasoning concerning the constituents of the brazing materials according to the invention will be given. It should be noted that the brazing material constituents all cooperate to give the desired properties. It is hence not possible to amend the percentage of one constituent and foresee the effect on the brazing material as a whole, concerning e.g. melting point, corrosion resistance, erosion and strength.

[0050] Concerning the balance, i.e. Iron (Fe), Iron is used for two reasons: the first reason is that it is a low cost metal and the second reason is that it will make a brazing material mimicking the base material to be brazed (in this case 316 or 304 stainless steel);

[0051] Nickel (Ni) will give the brazing material its austenitic properties. If less Nickel than defined above is used, the risk of excessive formation of ferritic phases in the brazing joint is increased. Also, there will be a risk that Nickel in the base material will migrate to the brazing joint during the brazing process, hence increasing the risk of formation of ferritic phases in the base material. If more Nickel than defined above is used, the cost of the brazing material will increase.

[0052] The Chromium (Cr) content will give the brazing joint its corrosion resistancesmaller amounts than defined above will give less corrosion resistance, while larger amounts will increase the cost of the brazing material and influence the melting temperature of the brazing material in a non-desired manner. Increased amounts of Chromium will, however, increase the melting temperature. Chromium also works as a ferrite stabilizerby adding an amount of Chromium to the brazing material that about equals the amount of Chromium in the material to be brazed, the base material composition is mimicked.

[0053] Molybdenum (Mo) will also increase the corrosion resistance of the brazing material. If less Molybdenum than defined above is used, the corrosion resistance will decrease. Molybdenum is an expensive metalhence, the cost of the brazing material will increase if more Molybdenum is used. Moreover, Molybdenum is a ferrite stabilizer, and the used level is tailored to mimic the austenitic base material to be brazed.

[0054] Manganese (Mn) is a constituent that reduces the erosion of the base material, i.e. the material being joined by brazing. The Manganese will evaporate during the brazing process, at least to some extent, and excessive amounts of manganese is added to the brazing material, the evaporated Manganese will foul the interior of the brazing furnaces in which the brazing is performed. However, in the percentages given above, the Manganese will reduce erosion significantly, without causing too much fouling of the furnace interior or the vacuum pumps used to pump out gas from the furnace in case it is desired to use vacuum during the brazing. Moreover, Manganese is an austenite stabilizer, and will to some extent counteract the melt depressant Silicon, which is a ferrite stabilizer. In the prior art, the austenite stabilizing properties seem to be neglected, just like its erosion reducing properties. Also, the interaction between the Silicon and the Manganese properties when it comes to ferrite/austenite formation are not mentioned in conjunction with brazing material.

[0055] Silicon (Si) is added for reduction of the melting temperature. It also increases the wettability of the brazing material to the base material. If less Silicon than defined is used, the melting point of the brazing material is not decreased sufficiently, while more Silicon than defined above will give a weaker brazing joint, due to formation of brittle Silicide phases. Moreover, the erosion of the base material increases with large amounts of Silicon.

[0056] Boron (B) is also added for depressing the melting point. However, it has turned out that the Boron may react with the other constituents of the brazing material and the base material to form borides, primarily chromium borides, which are very brittle and hence decreases the strength of the brazing joints. Increased amounts of Boron will worsen the corrosion properties. However, in the amounts defined above, the boride formation and corrosion resistance have turned out to be within acceptable limits.

[0057] One desired feature of the brazing material is that the liquidus temperature should be below 1170 degrees C. A liquidus temperature of 1190 degrees C. may, however, be acceptable in some cases. According to an embodiment, the brazing material has a liquidus temperature of less than 1170 degrees C., e.g. 1160 degrees C.

[0058] It is also important the erosion properties, i.e. that the brazing material entrains the base material and lowers its melting temperature, such that the base material melts, are acceptable.

[0059] In order to attain a suitable brazing material, a test has been carried out on the following brazing material compositions:

TABLE-US-00001 TABLE 1 the percentages of the respective element are given as weight percent. Alloy_Lot_No C S Mo Ni Cr Si Mn Fe B T_sol T_liq G118 0.04 0.009 2.04 13.3 18.1 7.9 5.1 Bal. 1.08 1115 1160 G227 0.043 0.005 2.04 13.4 18.9 8.1 5.3 Bal. 1.04 1110 1163 G228 0.057 0.004 2.18 13.5 18.6 7.8 5.5 Bal. 2.05 1088 1145 G35 0.029 0.003 2.1 12.8 17 12.4 0 Bal. 1.9 1127 1200 G68 0.07 0.004 2.16 12.8 16.8 11.6 0 Bal. 2.02 1130 1195 G69 0.041 0.003 1.87 12.8 17.5 10.7 0 Bal. 1.92 1133 1172 G7 0.017 0.003 1.87 13.1 17.4 12.7 0 Bal. 2.1 1131 1201 G71 0.047 0.005 2.04 13.4 17 8.16 3.16 Bal. 2 1093 1165 G72 0.073 0.009 1.99 13.4 17.2 10.7 2.97 Bal. 1.99 1107 1170 G74 0.03 0.005 2.14 13.7 17.3 7 5.2 Bal. 2.03 1092 1170

[0060] For these materials, DTA-TGA measurements, tensile strength tests, erosion tests and corrosion tests have been performed.

[0061] In FIG. 1 a, DTA-TGA measurements for the brazing alloys G74, G71, G72 and G69 are shown. As can be noted, the melting temperatures for these materials ranges from 1092 degrees C. (for G74) to 1133 degrees C. (for G69) it can further be noted that there is a distinct DSC peak at 1092 degrees C. for the G72 brazing material, indicating that one component of the brazing material will start to melt that the rest of the brazing material.

[0062] In FIG. 1b, DTA-TGA measurements for the brazing alloy G118 is shown. As can be noted, this material is completely melted at 1160 degrees C., and there is also a slight peak at 1115 degrees C., indicating that some of the material melts at this temperature.

[0063] Surprisingly, it has been found that the erosion, i.e. the phenomenon that the brazing material, or at least the melting point depressants thereof, has a minimum (it is desired with an as low erosion as possible) for 3-5.5% Manganese. Moreover, it has been found that Silicon in amounts of more than 9% rapidly increases erosion. In FIG. 2, Plots of erosion as a function of Silicon, Manganese and Boron percentages are shown. As can be seen, the erosion increases rapidly above 8-9% Silicon, while Manganese percentages above 3% decrease the erosion. When it comes to the content of Boron, the results are indecisive.

[0064] In FIG. 3, a scatterplot showing erosion ratio on the X-axis and the difference between brazing temperature and melting temperature is shown. As can be seen in this plot, the brazing alloys G71 and G74 stand out when it comes to low erosion. Although G72 has similar Mn content as G71, the higher Si content in G72 seems to increase the erosion rate. The erosion ratio is defined as (h.sub.0h.sub.1)/h.sub.0, wherein h.sub.0 is the material thickness before brazing and h.sub.1 is the undissolved material thickness after brazing.

[0065] Another effect of addition of Manganese is that the solidus and liquidus temperatures of the brazing material after the brazing cycle will be higher than the solidus and liquidus temperatures under a brazing cycle. This is due to the Manganese, which has liquidus lowering properties, vaporizing during the brazing operation, meaning that if the brazed article is reheated after the brazing, it must be heated to a higher temperature before the brazing joints melt. The vaporized Manganese will not entrain into the base material; rather, it will leave the furnace in which the brazing is performed through the vacuum pumps usually deployed to evacuate the furnace. The Boron, which as mentioned also has some liquidus lowering properties, will also to some extent leave the brazing material, since it will migrate into the base material during the brazing cycle, hence increasing the solidus and liquidus temperatures of the brazing material.

[0066] In order to manufacture a brazing material according to the invention, it is preferred to blend alloys containing some or all of the desired metals of the brazing material according to the invention, and/or elemental metal, and melt the blend to form a uniform alloy containing all the desired elements in the desired percentages. It should be noted that vaporizing of the Manganese during the blending and consecutive melting of the brazing material can be avoided if the melting is performed in a protective atmosphere rather than under vacuum. Once melted and blended, the alloy is poured into one or several molds and allowed to solidify to form ingots of brazing alloy. It should be noted that in some cases, it might be suitable to use rather small molds for obtaining small ingots, since there might be a small risk that the elements of the brazing alloy might separate during the solidification in the mold.

[0067] After the ingots have solidified, they are crushed. In order to even out possible differences between the compositions of the ingots, a batch of powder may be mixed. The powder is then mixed with a binder to form a paste.

[0068] More common methods of forming a powder are, however, water or gas atomization.

[0069] In another embodiment of the invention, the brazing material is made in form of ribbons or foils, e.g. by melt spinning.

[0070] Corrosion tests were performed by subjecting braze joints to salt spray for up to four weeks. It was found that the G118 braze material exhibited the best corrosion results. Generally, an overall increased amount of melt depressants, e.g. Si, B, seems to increase the corrosion; consequently, it is preferred to keep Si below 8%. However, the high percentage of Boron in the G74 increases the risk of formation of chromium borides, which may lead to brittle phases in and around the brazing joint.

[0071] The excellent properties of the G118 braze material come at a pricethe melting temperature of this brazing material is considerably higher than for prior art brazing materials. Historically, it has been desired to use Iron based brazing materials having a considerably lower melting temperature than the base material to be brazed. The brazing temperature has been kept slightly above the melting temperature of the brazing material. The prime reason for this approach has been to reduce erosion of the base material, which, as mentioned above, results due to melting point depressant migrating into the base material such that its melting temperature decreases.

[0072] However, surprisingly it has been found that by using the brazing material of the invention and high brazing temperatures, i.e. above 1200 degrees C., preferably above 1230 degrees C., brazing joints exhibiting high strength, limited corrosion due to entrainment of melting point depressant into base material and excellent corrosion resistance at a reasonable price have been achieved.

[0073] Brazing Process

[0074] In order to get an as strong brazing joint as possible, it is important to control both the application of the brazing material to the items to be brazed and the process where the articles are brazed. A suitable brazing process for brazing articles of austenitic stainless steels with the brazing material according to the invention may e.g. comprise: [0075] Placing brazing material on or in close vicinity of portions to be brazed to one another; [0076] Placing the articles in a furnace; [0077] Heating the furnace to a temperature such that the binder is vaporized and hold the temperature a time sufficient for the binder to be vaporised, hence leaving the powdered brazing material on the articles to be brazed; [0078] Heating the furnace to a temperature slightly below the melting temperature of the brazing material; [0079] Holding the furnace on the temperature slightly below the melting temperature for a time period sufficient to equalize the temperature in the furnace and the load, i.e. the articles to be brazed; [0080] Heating the temperature in the furnace to a temperature sufficient to melt the brazing material but insufficient to melt the material from which the articles to be brazed are manufactured; [0081] Cooling the furnace such that the brazing material solidifies and the brazed articles may be removed from the furnace.

[0082] Very promising results have been achieved by placing the brazing material around, not at, the joint to be brazed. This brazing method has been thoroughly disclosed in Swedish patent application 1351284-3, filed by SWEP International on Oct. 29, 2013, and has proven to give excellent brazing results when combined with the brazing material according to the invention.

[0083] One reason for the excellent result of the combination between the brazing method of Swedish patent application 1351284-3 and the brazing material according to the present invention may be the high temperatureby placing the brazing material such that no brazing material is located between the surfaces to be brazed to one another, the diffusion bonding between the surfaces to be brazed increases (due to the parts coming in close contact with one another), and diffusion brazing increases with increasing temperature.

[0084] Concerning the strength of the brazing joint, it is often found that the brazing joint has a strength exceeding the theoretical strength of the brazing material. Tests have shown that this might be due to the diffusion or trans liquid phase bonding processif the items to be joined are located very close to one another during the brazing process, the base material of the items to be joined will start to migrate into one another, such that a metallic bond is formed without or with minimal melting of the base material. This also reduces the amount of brittle phases (e.g. nickel silicides and chromium borides) in the joint.

[0085] The bonding process becomes more rapid the higher the temperature isthis is probably one of the reasons for the strong brazing joints achieved by using the brazing material according to the present invention, which demands for a high brazing temperature due to the comparatively high melting point of the brazing material and allows for a high brazing temperature with low erosion of the base material due to the low erosion properties of the brazing material.