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| 1. | Is AL-6XN stainless steel? |
7. | Can I weld AL-6XN by hand? |
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| 2. | Can I weld AL-6XN to 316L stainless steel? | 8. | Do I need to passivate a system constructed of AL-6XN? |
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| 3. | Are there special welding procedures that have to be followed? |
9. | Aren't all 6-moly materials the same? |
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| 10. | How much longer can I expect a system fabricated from AL-6XN to last over 316L? |
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| 4. | What is a weld insert ring? |
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| 5. | Is one style or material of insert ring better than the other? |
11. | Will AL-6XN help or eliminate my rouging problem? |
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| 12. | What type of application is best suited for AL-6XN? |
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What happens if I don't use the insert rings and don't anneal after welding? |
13. | How can I justify the cost of AL-6XN? |
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1. Is AL-6XN stainless steel? 2. Can I weld AL-6XN to 316L stainless steel? When welding the two materials together, as stated previously, chemical segregation of the molybdenum and chromium will occur in the heat-affected zone of the weld area. This increases the odds for crevice corrosion and pitting to occur under oxides on the surface of the weld areas. Due to the chemical composition of these materials during weld segregation, 316L actually becomes less noble when coupled by welding than if the two materials were joined together by clamping or bolting, and even these unions cannot eliminate the potential for galvanic corrosion. Dependent on the severity of the service and if indeed it is a borderline application between AL-6XN and 316L, the mixing of the two metals in the melt most likely would not be attacked. However, if the intended service is indeed very corrosive, the heat affected zone just past the weld in the 316L joining more than likely would be preferentially attacked. 3. Are there special welding procedures that have to be followed? 4. What is a weld insert ring? 5. Is one style or material of insert ring better than the other? 6. What happens if I don't use the insert rings and don't anneal after welding? 7. Can I weld AL-6XN by hand? 8. Do I need to passivate a system constructed of AL-6XN? 9. Aren't all 6-moly materials the same? 10. How much longer can I expect a system fabricated from AL-6XN to last over 316L? 11. Will AL-6XN help or eliminate my rouging problem? Class I is the most prevalent type found in pharmaceutical systems; it is caused from the erosion of centrifugal pump components, impellers, volutes and venturi on the back of the pump, and cracked valves. You can see the erosion of the softer material primarily the austenite away from the heavier material which is the nickel poor ferrites. When you look at the eroded areas with a scanning electron microscope you can see the ghosts of the dendritic structures. The softer parts are blasted out by the higher velocity water (sonic velocities). What happens is the higher velocity waters erode the tips of the impellers and all other items in its path, as soon as it gets into the tube it drops velocity back to std flow velocity (approx. 5 ft per second) and drops out everything it has picked up. The metal particles are attracted to the metal walls by electrostatic actions and gather on the walls. Concentrations are always heavier in the area from the pump outlet to some distance down stream. In these areas the particles will oxidize in the WFI because this is a superior oxidizing agent and begins to develop oxide films. Class I is strictly a function of the pump and the velocities. Type I - the red oxide - is due to the formation of hematites (Fe2O3), yellow oxide is hydrated hematites which is water stuck on to the molecule. Any material used down stream will rouge where Class I rouging is occurring. Class II comes from the metal itself, and it is usually caused by a corrosion mechanism eating into the passive layer. Usually this form of rouging occurs in systems that have not been chemically passivated. This is why it is so critical all WFI systems are passivated with nitric or citric acid. Class II rouging forms when little pustules developing on the surface explode, leaving brilliant silver spots under them. These are active sites of rouging, known as "in-situ rouging." Type II is primarily hematite (Fe2O3). AL-6XN will help this form of rouging tremendously. Class III is high temperature rouging and develops a heavy black film (magnetite Fe2O3) on the surface. If the surface has been electro polished this film will appear glossy black. If the system is non-passivated it becomes a powdery black. The glossy black is extremely stable. If you strip it off, re-passivate and pass high temp steam through it again. It will reform in a matter of months. In most cases you don't worry about this form of rouging. The powdery black surface is not stable and can release particles into the product. Currently, not enough data has been collected to determine if AL-6XN will help this form of rouging. In summary, AL-6XN will not help in class I rouging problems. However, class II rouging applications will see a definite benefit from the use of AL-6XN. In class III formations, there is no data available at this time to make a determination; all indications state that AL-6XN will improve class III rouging problems but will not totally eliminate the problem in all cases. 12. What type of application is best suited for AL-6XN? 13. How can I justify the cost of AL-6XN? If you have a specific question regarding the use AL-6XN alloy, please e-mail your questions to Technical Assistance at CSI. |
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