PROCESS FOR PRODUCING CORROSION RESISTANT ALLOY CLAD METAL PIPES
20220226929 · 2022-07-21
Assignee
Inventors
Cpc classification
B32B15/011
PERFORMING OPERATIONS; TRANSPORTING
B32B15/04
PERFORMING OPERATIONS; TRANSPORTING
C23C26/00
CHEMISTRY; METALLURGY
B32B15/015
PERFORMING OPERATIONS; TRANSPORTING
F16L9/153
MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
International classification
Abstract
The present invention relates to a process for producing corrosion resistant alloy-clad metal pipes by: (a) providing one or more pipes to be clad; (b) providing an exothermic mixture; 5 (c) loading and distributing the exothermic mixture into the one or more pipes in a cladding assembly at a rotational speed suitable to generate a centrifugal force of at most 10 times the gravitational force; (d) igniting the loaded exothermic mixture using an ignition system at a rotational speed generating a centrifugal force of at least 50 times the gravitational force; 10 and (e) applying a post cladding pipe procedure.
Claims
1. A process for producing corrosion resistant alloy-clad metal pipes by: (a) providing one or more pipes to be clad; (b) providing an exothermic mixture; (c) loading and distributing the exothermic mixture into the one or more pipes in a cladding assembly at a rotational speed suitable to generate a centrifugal force of at most 10 times the gravitational force; (d) igniting the loaded exothermic mixture using an ignition system at a rotational speed generating a centrifugal force of at least 50 times the gravitational force; and (e) applying a post cladding pipe procedure.
2. The process according to claim 1, wherein the corrosion resistant alloy comprises stainless steels, copper-nickel alloys, cobalt super alloys or nickel super alloys.
3. The process according to claim 1, wherein an end cap having a center opening is attached to at least one end of the steel pipe, preferably to both ends of the steel pipe prior to loading.
4. The process according to claim 1, wherein the exothermic mixture comprises at least one transition metal oxide and at least one fuel.
5. The process according to claim 1, wherein the exothermic mixture further comprises other metals or alloys or their oxides, other oxides or fluorides.
6. The process according to claim 1, wherein the clad pipes as obtained in step (d) are contacted with a cooling medium.
7. The process according to claim 6, wherein the cooling medium is water, preferably a water spray or a water tank placed underneath the cladding assembly.
8. The process according to claim 1, wherein the transition metal oxide is selected from the group consisting of copper oxides, iron oxides, nickel oxide, chromium oxides, niobium oxides, cobalt oxides or molybdenum oxides, and tungsten oxides, and mixtures thereof.
9. The process according to claim 1, wherein the exothermic mixture further comprises as fuel a component selected from the group consisting of aluminium, calcium, magnesium, silicon and mixtures thereof, more preferably binary, ternary, or quaternary fuels selected from Al, Ca, Mg and Si, even more preferably binary, ternary, or quaternary fuels comprising at least Ca.
10. The process according to claim 1, wherein the exothermic mixture further comprises a metal selected from the group of copper, iron, nickel, chromium, cobalt, manganese, molybdenum, niobium, tantalum, tungsten, and the alloys thereof.
11. The process according to claim 1, wherein step (c) is performed using blade powder spreading, interior tubing, expandable interior cylinder, and/or rotational velocity variation.
12. The process according to claim 1, wherein the cladding assembly includes mechanical support, an ignition system, and a cooling system.
13. The process according to claim 12, wherein the mechanical support includes a spring shock loaded mechanism to dynamically position and confine the pipe in rotation by confining wheels.
14. The process according to claim 1, wherein green pellets prepared by uniaxial pressing of the exothermic mixture, resistant wire, and a power supply are placed inside the pipes.
15. The process according to claim 1, wherein loading the exothermic mixture to the steel pipes is performed at a rotational velocity generating a centrifugal force of at least 1 g, more preferably at least 2 g and at most 10 g, more preferably at most 8 g.
16. The process according to claim 1, wherein igniting the exothermic mixture using an ignition system is performed at a rotational velocity generating a centrifugal force of at least 100 g, preferably at least 150 g.
17. The process according to claim 1, wherein the cladding assembly comprises an array of water spraying nozzles.
18. The process according to claim 1, wherein the post-cladding pipe procedure includes subjecting the slag layer to a mechanical ablative treatment, including breaking off slag by mechanical means, more preferably by mechanical means assisted by thermal shock due to cooling water spraying and/or by surface machining.
19. The process according to claim 1, wherein the interior of the one or more pipes are subjected to a thorough cleaning step prior to the cladding comprising by sand blasting and/or by using a chemical wash treatment followed by drying.
20. The process according to claim 19, wherein the chemical wash treatment comprises contacting the steel pipe surface with a weak acid, preferably acetic acid, more preferably in an aqueous solution.
21. The process according to claim 20, wherein the concentration of the acetic acid is between 1 and 10 vol %, preferably between 4 and 6 vol %.
Description
[0057] The following, non-limiting embodiments of the invention are further described hereinafter with reference to the accompanying figures, wherein like letters and numerals refer to like parts, wherein the figures are approximately to scale, and wherein:
[0058]
[0059]
[0060]
[0061]
[0062]
[0063]
[0064] Prior the clad operation, the backing pipe is preferably prepared by removing rust and grease at the interior surface by for example sandblasting and/or by soaking the pipe in a 5% vinegar solution for at least 24 hours, following by water cleaning and drying.
[0065] The clad operation starts with placing the backing pipe (30) between the four wheels (20) and (40), and the exothermic powder mixture is loaded into the pipe and distributed by one of two methods. In the first method, the powder mixture is first loaded to the inside of the pipe, which is then rotated at a rotational speed, at a rotation per minute (RPM) corresponding to the generation of a gravitational force of 2 g or higher. A device consisting of a blade (110) made of steel (or any other material), guide tracks (120) and adjusting screw (130) as illustrated in
[0066] In the another method, a combustible, e.g. paper, wax or carton tube (210) is placed inside at the centre of the backing pipe (220) as illustrated in
[0067] In still another method, the powder mixture is loaded to the inside of the pipe. The pipe is then rotated at a rotational velocity in RPMs that generates a gravitational force less than 1 g to allow the powder mixture to tumble initially, then the rotational velocity is increased to higher g-levels until it reached about 4 g. The rotational velocity is increased slowly and continuously to allow the inner powder to continue to tumble until the powder is distributed with a uniform layer thickness around the inner circumference of the backing pipe. This method is referred to as the RPM variation method.
[0068] Once the powder mixture is loaded to the clad pipe, the rotation of the pipe is increased to a higher rotational velocity to generate a gravitational force of at least 50 g. The powder is then ignited by using a setup illustrated in
[0069] The required rotational velocity during the reaction is selected according to the combustion temperature of the reaction, compositions of the CRA and slag, and the diameter of the pipe. Typically, it is in the range of 500-2000 RPM, generating a gravitational force of 50-300 g depending on the diameter of the pipes.
[0070] Shortly after the completion of the reaction, the pipe is cooled by water quenching, as shown in
[0071] The final clad pipe is illustrated in
[0072] The final step of the manufacture process involves removing the slag thus exposing the CRA. In most cases, slag can be easily broken off by mechanical operation. The slag removal can also be assisted by thermal shock, i.e., spraying the slag with water while it is still hot thus cracking and weakening the slag.
[0073] Optionally, the clad pipe may be heat treated post-clad to obtain the desired microstructure and properties for the backing pipe and clad layer.
[0074] The following, non-limiting examples are provided to illustrate the invention. The clad pipe manufacture process is illustrated in the following using stainless steel as CRA examples.
[0075] For all examples except for example 8, a section of X60 carbon steel pipe having an outside diameter of 273.1 mm, a wall thickness of 11.1 mm and a length of 500 mm was cleaned by sand blasting and soaking in 5% white vinegar for 24 hours.
[0076] After loading the different exothermic mixtures, the ignition set up shown in
[0077] For all examples, the pipe was cooled shortly after the completion of the reaction, by spraying water from both inside and outside. Water spraying from inside the pipe leads to the weakening of the slag by thermal shocking, thus the slag could be readily removed from a subsequent mechanical operation.
Example 1
[0078] An exothermic mixture containing iron oxide (Fe.sub.2O.sub.3), calcium (Ca) and aluminum (Al), and alloying metals of chromium (Cr), nickel (Ni), iron (Fe), molybdenum (Mo), silicon (Si), and manganese (Mn) was loaded to the inside of the pipe by the BPS method while the pipe was in rotation at approximately 250 RPM (.sup.˜8 g). Afterward, the rotational velocity was raised to 1150 RPM (.sup.˜185 g) and the mixture was ignited. Shortly after the completion of the reaction, the pipe was cooled by spraying water.
[0079] Upon the ignition and reaction, the mixture formed molten CRA of stainless steel 316L composition and a molten slag of oxides (CaO and Al.sub.2O.sub.3). Owing to the large difference in specific gravities between the CRA and the slag, the CRA was deposited to the inner wall of the X60 backing pipe with the slag on top. Shortly after the completion of the reaction, the pipe was cooled by spraying water from both inside and outside and slag was removed using a separate mechanical operation. Examination of the cross sections of the cladded pipe showed that a strong metallurgical bond had been formed between the cladded layer and the X60 steel backing.
Example 2
[0080] An exothermic mixture containing iron oxide (Fe.sub.2O.sub.3), chromium oxide (Cr.sub.2O.sub.3), calcium (Ca) and aluminum (Al), and alloying metals of chromium (Cr), nickel (Ni), iron (Fe), molybdenum (Mo), silicon (Si), and manganese (Mn) was loaded to the inside of the pipe by the paper tube (PT) method. Afterward, the rotational velocity was raised to 1150 RPM (.sup.˜185 g) and the mixture was ignited. Shortly after the completion of the reaction, the pipe was cooled by spraying water.
[0081] Upon the ignition and reaction, the mixture formed molten CRA of stainless steel 316L composition and molten slag of oxides (CaO and Al.sub.2O.sub.3). Owing to the large difference in specific gravities between the CRA and the slag, the CRA was deposited to the inner wall of the X60 backing pipe with the slag on top. Shortly after the completion of the reaction, the pipe was cooled by spraying water from both inside and outside and slag was removed using a separate mechanical operation. Examination of the cross sections of the cladded pipe showed a strong metallurgical bond had been formed between the cladded layer and the X60 steel backing.
Example 3
[0082] An exothermic mixture containing iron oxide (Fe.sub.2O.sub.3), calcium (Ca) and aluminum (Al), and alloying metals of chromium (Cr), nickel (Ni), iron (Fe), molybdenum (Mo), silicon (Si), and manganese (Mn) was loaded to the inside of the pipe. The powders were tumbled using a rotational velocity that generates a gravitational force of about 0.5 g for 30 seconds. The rotational velocity or rotational speed is then gradually increased to generate a gravitational force of 4 g with about 5 minutes taken to transition from 0.5 g to 4 g. Afterward, the rotational velocity was raised to 1150 RPM (.sup.˜185 g) and the mixture was ignited. Shortly after the completion of the reaction, the pipe was cooled by spraying water.
[0083] Upon the ignition and reaction, the exothermic mixture forms molten CRA of stainless steel 316L composition and molten slag of oxides (CaO and Al.sub.2O.sub.3). Owing to the large difference in specific gravities between the CRA and the slag, the CRA was deposited to the inner wall of the X60 backing pipe with the slag on top. Shortly after the completion of the reaction, the pipe was cooled by spraying water from both inside and outside and slag was removed using a separate mechanical operation. Examination of the cross sections of the cladded pipe showed a strong metallurgical bond has been formed between the cladded layer and the X60 steel backing.
Example 4
[0084] An exothermic mixture containing iron oxide (Fe.sub.2O.sub.3), calcium (Ca) and aluminum (Al), fluorspar (CaF.sub.2) and alloying metals of chromium (Cr), nickel (Ni), iron (Fe), molybdenum (Mo), silicon (Si), and manganese (Mn) was loaded to the inside of the pipe by the BPS method while the pipe was in rotation at approximately 250 RPM (.sup.˜8 g). Afterward, the pipe was rotated at 1150 RPM (.sup.˜185 g) and the mixture was ignited. Shortly after the completion of the reaction, the pipe was cooled by spraying water.
[0085] Upon the ignition and reaction, the mixture forms molten CRA of stainless steel 316L composition and a molten slag made of oxides (CaO and Al.sub.2O.sub.3) and fluoride (CaF.sub.2). Owing to the large difference in specific gravities between the CRA and the slag, the CRA was deposited to the inner wall of the X60 backing pipe with the slag on top. Shortly after the completion of the reaction, the pipe was cooled by spraying water from both inside and outside and slag was removed using a separate mechanical operation. Examination of the cross sections of the cladded pipe showed a strong metallurgical bond has been formed between the cladded layer and the X60 steel backing.
Example 5
[0086] An exothermic mixture containing iron oxide (Fe.sub.2O.sub.3), calcium (Ca), silicon (Si) and aluminum (Al) and alloying metals of chromium (Cr), iron (Fe), nickel (Ni), molybdenum (Mo), and manganese (Mn) was loaded to the inside of the pipe by the BPS method while the pipe was in rotation at approximately 250 RPM (.sup.˜8 g). Afterward, the rotation speed was raised to 1150 RPM (.sup.˜185 g) and the mixture was ignited. Shortly after the completion of the reaction, the pipe was cooled by spraying water.
[0087] Upon the ignition and reaction, the mixture forms molten CRA of stainless steel 316L composition and a molten slag of oxides (CaO, SiO.sub.2 and Al.sub.2O.sub.3). Owing to the large difference in specific gravities between the CRA and the slag, the CRA was deposited to the inner wall of the X60 backing pipe with the slag on top. Shortly after the completion of the reaction, the pipe was cooled by spraying water from both inside and outside and slag was removed using a separate mechanical operation. Examination of the cross sections of the cladded pipe showed a strong metallurgical bond has been formed between the cladded layer and the X60 steel backing.
Example 6
[0088] An exothermic mixture containing iron oxide (Fe.sub.2O.sub.3), nickel oxide (NiO), chromium oxide (Cr.sub.2O.sub.3), calcium (Ca), aluminium (Al), and silicon (Si) and alloying metals of iron (Fe), molybdenum (Mo), and manganese (Mn) was loaded to the inside of the pipe by the BPS method while the pipe was in rotation at approximately 250 RPM (.sup.˜8 g). Afterward, the rotation speed was raised to 1150 RPM (.sup.˜185 g) and the mixture was. Shortly after the completion of the reaction, the pipe was cooled by spraying water.
[0089] Upon the ignition and reaction, the mixture forms molten CRA of stainless steel 316L composition and a molten slag of oxides (CaO, Al.sub.2O.sub.3 and SiO.sub.2). Owing to the large difference in specific gravities between the CRA and the slag, the CRA was deposited to the inner wall of the X60 backing pipe with the slag on top. Shortly after the completion of the reaction, the pipe was cooled by spraying water from both inside and outside and slag was removed using a separate mechanical operation. Examination of the cross sections of the cladded pipe showed a strong metallurgical bond has been formed between the cladded layer and the X60 steel backing.
Example 7
[0090] An exothermic mixture containing iron oxide (Fe.sub.2O.sub.3), calcium (Ca), aluminium (Al) and silicon (Si), and alloying metals of chromium (Cr), nickel (Ni), iron (Fe), molybdenum (Mo), silicon (Si), and manganese (Mn) was loaded to the inside of the pipe by the BPS method while the pipe was in rotation at approximately 250 RPM (.sup.˜8 g). Afterward, a calculated amount of silica (SiO.sub.2) was loaded to the inside of the pipe by the BPS method while the pipe was in rotation. Then the pipe was rotated at 1150 RPM (.sup.˜185 g) and the mixture was ignited. Shortly after the completion of the reaction, the pipe was cooled by spraying water.
[0091] Upon the ignition and reaction, the mixture forms molten CRA of stainless steel 316L composition and a molten slag made of oxides (CaO, Al.sub.2O.sub.3 and SiO.sub.2). Owing to the large difference in specific gravities between the CRA and the slag, the CRA was deposited to the inner wall of the X60 backing pipe with the slag on top. Shortly after the completion of the reaction, the pipe was cooled by spraying water from both inside and outside and slag was removed using a separate mechanical operation. Examination of the cross sections of the cladded pipe showed a strong metallurgical bond has been formed between the cladded layer and the X60 steel backing.
Example 8
[0092] A section of X60 carbon steel pipe having an outside diameter of 273.1 mm, a wall thickness of 11.1 mm and a length of 500 mm was not cleaned and used “as is” although it was exposed to the environment for a few years and contained visible rust. An exothermic mixture containing iron oxide (Fe.sub.2O.sub.3), nickel oxide (NiO), calcium (Ca), aluminium (Al) and silicon (Si), and alloying metals of chromium (Cr), iron (Fe), molybdenum (Mo), silicon (Si), and manganese (Mn) was loaded to the inside of the pipe by the BPS method while the pipe was in rotation at approximately 250 RPM (.sup.˜8 g). Afterward, the pipe was rotated at 1150 RPM (.sup.˜185 g) and the mixture was ignited. Shortly after the completion of the reaction, the pipe was cooled by spraying water.
[0093] Upon the ignition and reaction, the mixture forms molten CRA of stainless steel 316L composition and a molten slag made of oxides (CaO, Al.sub.2O.sub.3 and SiO.sub.2). Owing to the large difference in specific gravities between the CRA and the slag, the CRA was deposited to the inner wall of the X60 backing pipe with the slag on top. Shortly after the completion of the reaction, the pipe was cooled by spraying water from both inside and outside and slag was removed using a separate mechanical operation. Examination of the cross sections of the cladded pipe showed a strong metallurgical bond has been formed between the cladded layer and the X60 steel backing.
[0094] The above examples for manufacture of stainless steel 316L cladded pipes can be extended to the manufacturing of other CRA clad pipes such as other stainless-steel compositions, nickel super alloys, and copper nickel alloys using appropriate transition metal oxides, thus manufacture of these CRA cladded pipes are also included in the scope of the current invention.