US3351684A - Method of reducing carbon deposits on surfaces in contact with carbonaceous gases and subjected to elevated temperatures - Google Patents
Method of reducing carbon deposits on surfaces in contact with carbonaceous gases and subjected to elevated temperatures Download PDFInfo
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- US3351684A US3351684A US437676A US43767665A US3351684A US 3351684 A US3351684 A US 3351684A US 437676 A US437676 A US 437676A US 43767665 A US43767665 A US 43767665A US 3351684 A US3351684 A US 3351684A
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- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 title claims description 33
- 229910052799 carbon Inorganic materials 0.000 title claims description 33
- 238000000034 method Methods 0.000 title claims description 13
- 239000007789 gas Substances 0.000 title description 43
- 230000008021 deposition Effects 0.000 claims description 14
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 5
- 229910052708 sodium Inorganic materials 0.000 claims description 5
- 239000011734 sodium Substances 0.000 claims description 5
- 239000000463 material Substances 0.000 description 10
- 229910052782 aluminium Inorganic materials 0.000 description 7
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 7
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 7
- 235000012239 silicon dioxide Nutrition 0.000 description 6
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 5
- 229910052802 copper Inorganic materials 0.000 description 5
- 239000010949 copper Substances 0.000 description 5
- 239000010453 quartz Substances 0.000 description 5
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 4
- 230000009471 action Effects 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 230000009467 reduction Effects 0.000 description 3
- 238000005070 sampling Methods 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 2
- 229910045601 alloy Inorganic materials 0.000 description 2
- 239000000956 alloy Substances 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 238000005255 carburizing Methods 0.000 description 2
- 238000004140 cleaning Methods 0.000 description 2
- 238000005336 cracking Methods 0.000 description 2
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 2
- 229910052737 gold Inorganic materials 0.000 description 2
- 239000010931 gold Substances 0.000 description 2
- 229910052752 metalloid Inorganic materials 0.000 description 2
- 150000002738 metalloids Chemical class 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 239000007800 oxidant agent Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052697 platinum Inorganic materials 0.000 description 2
- 229910052709 silver Inorganic materials 0.000 description 2
- 239000004332 silver Substances 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- WURBVZBTWMNKQT-UHFFFAOYSA-N 1-(4-chlorophenoxy)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)butan-2-one Chemical compound C1=NC=NN1C(C(=O)C(C)(C)C)OC1=CC=C(Cl)C=C1 WURBVZBTWMNKQT-UHFFFAOYSA-N 0.000 description 1
- 229910000851 Alloy steel Inorganic materials 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- 238000006219 Matteson homologation reaction Methods 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 229910002091 carbon monoxide Inorganic materials 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 230000003628 erosive effect Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D1/00—General methods or devices for heat treatment, e.g. annealing, hardening, quenching or tempering
- C21D1/68—Temporary coatings or embedding materials applied before or during heat treatment
- C21D1/72—Temporary coatings or embedding materials applied before or during heat treatment during chemical change of surfaces
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C8/00—Solid state diffusion of only non-metal elements into metallic material surfaces; Chemical surface treatment of metallic material by reaction of the surface with a reactive gas, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals
- C23C8/06—Solid state diffusion of only non-metal elements into metallic material surfaces; Chemical surface treatment of metallic material by reaction of the surface with a reactive gas, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using gases
- C23C8/08—Solid state diffusion of only non-metal elements into metallic material surfaces; Chemical surface treatment of metallic material by reaction of the surface with a reactive gas, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using gases only one element being applied
- C23C8/20—Carburising
- C23C8/22—Carburising of ferrous surfaces
Definitions
- This invention relates to a method for substantially reducing undesirable carbon deposits onto surfaces from carbonaceous gases, and more particularly to a method of providing a means at the inner surface of at least a cer tain portion of a passage for reducing deposition of carbon from carbonaceous gases carried in the passage.
- a carbonaceous gaseous atmosphere in a heat-treating furnace to aid in the treatment of parts therein, for example, to cause an extremely hard surface to be formed on the parts, is well known.
- the carbonaceous gas is usually supplied through an inlet passage or tube extending through a wall of the furnace.
- the present invention is based upon the discovery that certain material can be applied to the inner surfaces of passages or tubes through which carbonaceous gases fiow to substantially reduce build-up or deposition of carbon therein. More specifically, it has been found that materials effective in accomplishing this result are those having a positive standard electrode potential, based upon the standard electrode potential of sodium as being negative. Hence, the effectiveness of the materials at the inner surface of the passages is achieved because the deposition of the carbon is caused by an electromotive force and not by cracking of the gases, as has heretofore been commonly believed. In retrospect, it is believed that one part of the tube may act as an anode and another part, contiguous with the first or spaced therefrom by a greater or lesser distance may act as a cathode.
- the carbonaceous atmosphere must undergo a composition change at temperatures within the indicated range to initiate the galvanic action and then serve as the electrolyte through which an electric current flows to cause erosion of the anode.
- the carbonaceous gas may simply act as an anode and the passage or tube in which the gas is carried may act as a cathode of a galvanic cell to cause the carbon deposition.
- the substantial reduction and, in most instances, elimination of the carbon deposition occur because of the passive nature of the material used, which tends to prevent the galvanic action. This result does not explain which type of galvanic action is involved;
- I907 ice carbon inserts can be used in those portions of a tube or passage subjected to a temperature Within the range of 11001300 F. to produce the desired effect.
- a coating of aluminum can be provided in the corresponding portion of the tube with substantially equal effectiveness, the exposed surface of the aluminum subsequently oxidizing.
- the copper has been found to be effective in de position reduction, it does have the disadvantage that it tends to oxidize when there are no carbonaceous gases passing through the tube and the copper is subjected to oxygen from the atmosphere.
- Other materials with a positive standard electrode potential include silver, platinum, gold, silicon, and metal and metalloid oxides.
- FIG. 1 is a schematic view in vertical cross section of a furnace and a tube made of a common material, showing typical carbon deposition within the: tube after a short period of operation;
- FIG. 2 is a graph showing the temperature along the length of the tube of FIG. 1;
- FIG. 3 is a view similar to FIG. 1 of a furnace and a gascarrying tube according to the invention, after operation for the same period of time.
- a furnace indicated at 10 has a tube 12 for carrying a carbonaceous gas.
- the tube 12 extends through a back wall 14, through a heating chamber 15, and through a front wall 16 of the furnace, but it is to be understood that the invention is not limited to a furnace or tube of a particular design.
- Carbonaceous gas is supplied to a rear inlet 18 of the tube 12 and enters the chamber 15 thorugh orifices 20.
- the front end of the tube beyond the front furnace wall 16 is closed by a cap 22.
- a carbon deposit 24 accumulates in a portion of the tube subjected to a temperature ranging from about 1100 to about 1300 F. and a somewhat smaller but still significant deposit 26 is formed at the stagnant end of the tube where a similar temperature range exists.
- the extent of the deposits depends upon a number of factors, including the concentration of carbon in the gas, the volume or rate of flow of gas, and the length of the tube in the 1100-1300" F. temperature range.
- the furnace 10 was maintained at a temperature of 1700 F. and the tube 112 was 8 /2. feet long with 1% inch I.P.S. Twenty-four of the orifices 20 were drilled centrally in the top of the tube 12 on two-inch centers and with inch diameters.
- the carbonaceous gas used was produced by adding 5% methane, by volume, to a gas which has a typical composition, by volume, of 0.1% CO 20.7% C0, 40.6% H 0.4% CH 0.3% H 0, and 37.9% N
- the gas was supplied through the tube 12 at a rate of cu. ft. per hour.
- the tube 12 was made of an alloy steel containing 15% of chromium, 35% of nickel; 0.25% maximum carbon, balance iron.
- the deposits 24 and 26 are shown as they existed after the carbonaceous gas was' supplied to the furnace it) for a period of eight hours.
- Thermocouples were located along the tube 12 to measure temperature distribution which was as shown in FIG. 2.
- the tube temperature ranges from near ambient at the inlet 18 to a high temperature of about 1700 F. at a point approximately three feet from the inlet 18, which point is approximately one-and-one-half feet from the inner surface of the back wall 14. Consequently, an intermediate part of the tube 12 extending through the wall 14 is subjected to temperatures Within the critical range of 1l001300 F. and it is in this area that the carbon deposition 24 occurs.
- a portion of the opposite end of the tube falls within the 11001300 F. range, although this portion is shorter since the temperature differential is sharper at the right hand end of the tube where the gas is stagnant.
- the components are identical to those shown in FIG. 1 except that the tube 12 now has a thin cylindrical quartz insert 28.
- This insert has a length suificient to cover the inner surface of the tube in the region which is at a temperature between 1100-1300 F. when the furnace is in operation.
- the insert 28 has an outer diameter equal to the inner diameter of the tube 12 and has a thickness sufficient to provide adequate strength and integrity for the insert.
- Another quartz insert 30 is also located in the tube at the right hand portion which is subjected to temperatures within the range of 11001300 F.
- the problem of carbon deposit is so great that carbonaceous gas-carrying tubes cannnot be used at all.
- a long alloy cylindrical retort extends horizontally through a furnace and is rotatably supported at its ends.
- the retort has an internal helical ridge which causes parts in the bottom of the retort to be moved along as the retort rotates.
- a carbonaceous gas is fed into the retort at one end for the purpose of carburizing parts, while the furnace is heated by enclosed radiant tubes, as is well known in the art.
- a ported carbonaceous gas-supplying tube be used in place of the usual tube which merely supplies the carbonaceous gas at one end of the retort.
- the ported type of tube would enable the carbonaceous gas to be supplied at particular portions of the retort in which the parts can be most effectively carburized.
- the heavy carbon deposits formed within ported tubes have rendered such use impractical. With the inserts according to the invention, such tubes can be used to advantage and without any plugging problem.
- inserts 28 and 30 in FIG. 3 have been described specifically as being quartz or silicon dioxide, the inserts can also equally effectively be made of carbon. Further, copper inserts have also been effective for the purpose but have the disadvantage that they oxidize when they are hot and are subjected to oxygen of the atmosphere. It has been found also that a coating can be applied to the interior surface of the tube to reduce or eliminate carbon deposition. For this purpose, a coating of aluminum can be applied to the tube in the critical portion thereof and no carbon deposit will be found in the coated portion of the tube. It is important inthe case of aluminum that no de-oxidizer be used in order that the aluminum surface is oxidized to alumina.
- any material can be used at the inner surface of the carbonaceous gas-carrying tube to reduce carbon deposits, if the material has a positive standard electrode potential, based upon the potential of sodium as being negative. This includes gold, platinum, and silver which are not commercially practical from a cost standpoint but, nevertheless, are effective from the standpoint of substantially reducing carbon deposits.
- the steps comprising: securing a tube in confluent relationship with a furnace, providing that portion of the tube having a temperature between 1100 and 1300 F. with a lining having a positive standard electrode potential, based upon the standard eiectrode potential of sodium as being negative, and passing the carbonaceous gas through said tube.
- the steps comprising: securing a tube in confluent relationship with a furnace, providing a positive electrode potential, based upon the standard electrode potential of sodium as being negative, to that portion of the tube having a temperature range of 1100 to 1300 F. and passing the carbonaceous gas through said tube.
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- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
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- Chemical Vapour Deposition (AREA)
Description
Nov- 7, 196 J. A. LINCOLN ,351,684
ON DEPOSITS ON SURFACES IN CONTACT WITH ATED TEMPERATURES METHOD OF'VREDUCING CARB CARBONACEOUS GASES AND SUBJECTED TO ELEV Filed March 8, 1965 2 TUBE EN6 77/ Iii.
00 man .PM ATT'YE United States Patent Ohio Filed Mar. 8, 1965, Ser. No. 437,676 8 Claims. (Cl. 263-52) This invention relates to a method for substantially reducing undesirable carbon deposits onto surfaces from carbonaceous gases, and more particularly to a method of providing a means at the inner surface of at least a cer tain portion of a passage for reducing deposition of carbon from carbonaceous gases carried in the passage.
The use of a carbonaceous gaseous atmosphere in a heat-treating furnace to aid in the treatment of parts therein, for example, to cause an extremely hard surface to be formed on the parts, is well known. In such furnaces, the carbonaceous gas is usually supplied through an inlet passage or tube extending through a wall of the furnace.
. In these furnaces and also in other applications using carbonaceous gases, it is common to remove part of the carbonaceous gases from the furnace or from other heated regions through sampling tubes, to determine the compositions of the gases.
In both the inlet passages or tubes and in the sampling tubes, it has been known that carbon is deposited from the gases and that the. deposits occur almost exclusively in portions of the tubes where the temperature is within the range of 1100-1300" F. For years, such deposits have been attributed to cracking of the gases and were considered to be impossible to eliminate, other than by periodic cleaning by physically removing the deposits from the tubes. In some instances, the deposits have occurred with sufficient rapidity that cleaning several times a week has been necessary, involving substantial labor costs and even sometimes requiring shutdown of the entire heattreating operation. In other instances, proposed systems for handling the carbonaceous gases in certain ways have had to be discarded because of the deposition problem.
The present invention is based upon the discovery that certain material can be applied to the inner surfaces of passages or tubes through which carbonaceous gases fiow to substantially reduce build-up or deposition of carbon therein. More specifically, it has been found that materials effective in accomplishing this result are those having a positive standard electrode potential, based upon the standard electrode potential of sodium as being negative. Apparently, the effectiveness of the materials at the inner surface of the passages is achieved because the deposition of the carbon is caused by an electromotive force and not by cracking of the gases, as has heretofore been commonly believed. In retrospect, it is believed that one part of the tube may act as an anode and another part, contiguous with the first or spaced therefrom by a greater or lesser distance may act as a cathode. The carbonaceous atmosphere must undergo a composition change at temperatures within the indicated range to initiate the galvanic action and then serve as the electrolyte through which an electric current flows to cause erosion of the anode. On the other hand, although less likely, the carbonaceous gas may simply act as an anode and the passage or tube in which the gas is carried may act as a cathode of a galvanic cell to cause the carbon deposition. Apparently, the substantial reduction and, in most instances, elimination of the carbon deposition occur because of the passive nature of the material used, which tends to prevent the galvanic action. This result does not explain which type of galvanic action is involved;
Specifically, tests have shown that copper, quartz, and
3,351,654 Patented Nov. 7, I907 ice carbon inserts can be used in those portions of a tube or passage subjected to a temperature Within the range of 11001300 F. to produce the desired effect. In addition a coating of aluminum can be provided in the corresponding portion of the tube with substantially equal effectiveness, the exposed surface of the aluminum subsequently oxidizing. These materials have been found to be most effective not only from the standpoint. of deposition reduction but also from the standpoint of material costs.
While the copper has been found to be effective in de position reduction, it does have the disadvantage that it tends to oxidize when there are no carbonaceous gases passing through the tube and the copper is subjected to oxygen from the atmosphere. Other materials with a positive standard electrode potential, and which could also be used, include silver, platinum, gold, silicon, and metal and metalloid oxides.
It is, therefore, a principal object of the invention to provide means for substantially reducing deposition of carbon from carbonaceous gases in the interior of passages or tubes through which gases are carried.
Other objects of the invention will be apparent from the following detailed description of a preferred embodiment thereof, reference being made to the accompanying drawings, in which:
FIG. 1 is a schematic view in vertical cross section of a furnace and a tube made of a common material, showing typical carbon deposition within the: tube after a short period of operation;
FIG. 2 is a graph showing the temperature along the length of the tube of FIG. 1; and
FIG. 3 is a view similar to FIG. 1 of a furnace and a gascarrying tube according to the invention, after operation for the same period of time.
Referring to FIG. 1, a furnace indicated at 10 has a tube 12 for carrying a carbonaceous gas. The tube 12 extends through a back wall 14, through a heating chamber 15, and through a front wall 16 of the furnace, but it is to be understood that the invention is not limited to a furnace or tube of a particular design. Carbonaceous gas is supplied to a rear inlet 18 of the tube 12 and enters the chamber 15 thorugh orifices 20. The front end of the tube beyond the front furnace wall 16 is closed by a cap 22. With this arrangement, the gas between the inlet 18 and the orifices 20 is constantly in motion whereas the gas between the front orifice 20 and the cap 22 is relatively stagnant.
As shown in FIG. 1, a carbon deposit 24 accumulates in a portion of the tube subjected to a temperature ranging from about 1100 to about 1300 F. and a somewhat smaller but still significant deposit 26 is formed at the stagnant end of the tube where a similar temperature range exists. The extent of the deposits depends upon a number of factors, including the concentration of carbon in the gas, the volume or rate of flow of gas, and the length of the tube in the 1100-1300" F. temperature range.
'In a specific example of operation of the apparatus of FIG. 1, the furnace 10 was maintained at a temperature of 1700 F. and the tube 112 was 8 /2. feet long with 1% inch I.P.S. Twenty-four of the orifices 20 were drilled centrally in the top of the tube 12 on two-inch centers and with inch diameters. The carbonaceous gas used was produced by adding 5% methane, by volume, to a gas which has a typical composition, by volume, of 0.1% CO 20.7% C0, 40.6% H 0.4% CH 0.3% H 0, and 37.9% N The gas was supplied through the tube 12 at a rate of cu. ft. per hour. The tube 12 was made of an alloy steel containing 15% of chromium, 35% of nickel; 0.25% maximum carbon, balance iron. The deposits 24 and 26 are shown as they existed after the carbonaceous gas was' supplied to the furnace it) for a period of eight hours.
Thermocouples were located along the tube 12 to measure temperature distribution which was as shown in FIG. 2. As can be seen from a direct comparison of FIGS. 1 and 2, the tube temperature ranges from near ambient at the inlet 18 to a high temperature of about 1700 F. at a point approximately three feet from the inlet 18, which point is approximately one-and-one-half feet from the inner surface of the back wall 14. Consequently, an intermediate part of the tube 12 extending through the wall 14 is subjected to temperatures Within the critical range of 1l001300 F. and it is in this area that the carbon deposition 24 occurs. Similarly, a portion of the opposite end of the tube falls within the 11001300 F. range, although this portion is shorter since the temperature differential is sharper at the right hand end of the tube where the gas is stagnant.
Referring more particularly to FIG. 3, the components are identical to those shown in FIG. 1 except that the tube 12 now has a thin cylindrical quartz insert 28. This insert has a length suificient to cover the inner surface of the tube in the region which is at a temperature between 1100-1300 F. when the furnace is in operation. Preferably, the insert 28 has an outer diameter equal to the inner diameter of the tube 12 and has a thickness sufficient to provide adequate strength and integrity for the insert. Another quartz insert 30 is also located in the tube at the right hand portion which is subjected to temperatures within the range of 11001300 F.
It was found that when the apparatus of FIG. 3 was operated as described above, referring to FIG. 1, no carbon deposit build-up whatsoever occurred in eight hours either on the insert 28 or on any part of the inner surface of the tube adjacent the insert 28. \Vliile a very fine layer of carbon appeared on the insert 30, it was much too fine to measure. As indicated previously, the latter layer apparently was caused by reduced solubility of the carbon in the gas at the lower temperatures. Even after the furnace was operated for approximately one week, no carbon deposit was found on or near the insert 23 and the deposit on the insert 36 was only slightly more than that existing after eight hours.
While the problem of carbon deposit has been discussed in connection with a ported tube, the deposit also is a problem with other tubes which are subjected to the 1100-1300 F. temperature range and which carry carbonaceous gases. This includes direct inlet tubes which supply gas directly into a carburizing furnace, for example, and also to sampling tubes by means of which carbonaceous atmosphere gases are withdrawn from a furnace chamber for purposes of testing.
In some instances, the problem of carbon deposit is so great that carbonaceous gas-carrying tubes cannnot be used at all. For example, in rotary retort furnaces, a long alloy cylindrical retort extends horizontally through a furnace and is rotatably supported at its ends. The retort has an internal helical ridge which causes parts in the bottom of the retort to be moved along as the retort rotates. A carbonaceous gas is fed into the retort at one end for the purpose of carburizing parts, while the furnace is heated by enclosed radiant tubes, as is well known in the art. It has heretofore been suggested that a ported carbonaceous gas-supplying tube be used in place of the usual tube which merely supplies the carbonaceous gas at one end of the retort. The ported type of tube would enable the carbonaceous gas to be supplied at particular portions of the retort in which the parts can be most effectively carburized. However, the heavy carbon deposits formed within ported tubes have rendered such use impractical. With the inserts according to the invention, such tubes can be used to advantage and without any plugging problem.
It has also been proposed heretofore that atmosphere gas be recirculated through atmosphere furnaces so that more effective use of the gas could be achieved. However, the problem of carbon deposits again made such proposals impractical since the tubes through which the gases were to be recirculated would quickly plug. With the tube inserts according to the invention, however, the use of such tubes is feasible.
While the inserts 28 and 30 in FIG. 3 have been described specifically as being quartz or silicon dioxide, the inserts can also equally effectively be made of carbon. Further, copper inserts have also been effective for the purpose but have the disadvantage that they oxidize when they are hot and are subjected to oxygen of the atmosphere. It has been found also that a coating can be applied to the interior surface of the tube to reduce or eliminate carbon deposition. For this purpose, a coating of aluminum can be applied to the tube in the critical portion thereof and no carbon deposit will be found in the coated portion of the tube. It is important inthe case of aluminum that no de-oxidizer be used in order that the aluminum surface is oxidized to alumina. If a de-oxidizer is used with the aluminum so that the oxide of the aluminum is not present, the carbon will build up even more rapidly than in the case of the bare alloy. Actually, as mentioned previously, any material can be used at the inner surface of the carbonaceous gas-carrying tube to reduce carbon deposits, if the material has a positive standard electrode potential, based upon the potential of sodium as being negative. This includes gold, platinum, and silver which are not commercially practical from a cost standpoint but, nevertheless, are effective from the standpoint of substantially reducing carbon deposits.
Various modifications of the abovedescribed embodiments of the invention will be apparent to those skilled in the art, and it is to be understood that such modifications can be made without departing from the scope of the invention, if they are Within the spirit and tenor of the accompanying claims.
I claim:
1. In the method of preventing deposition of carbon from a heated carbonaceous gas, the steps comprising: securing a tube in confluent relationship with a furnace, providing that portion of the tube having a temperature between 1100 and 1300 F. with a lining having a positive standard electrode potential, based upon the standard eiectrode potential of sodium as being negative, and passing the carbonaceous gas through said tube.
2. The method of claim 1 wherein said lining is a metallic oxide.
3. The method of claim 1 wherein said lining is a metalloid oxide.
4. The method of claim 1 wherein said lining is aluminum oxide.
5. The method of claim 1 wherein said lining is carbon.
6. The method of claim 1 wherein said lining is quartz.
7. The method of claim 1 wherein said lining is copper.
8. In the method of preventing the deposition of carbon from a heated carbonaceous gas, the steps comprising: securing a tube in confluent relationship with a furnace, providing a positive electrode potential, based upon the standard electrode potential of sodium as being negative, to that portion of the tube having a temperature range of 1100 to 1300 F. and passing the carbonaceous gas through said tube.
References Cited UNITED STATES PATENTS 884,181 4/1908 Machlet 14S16.5 X 2,604,936 7/1952 Kaehni et al. 26352 X 2,648,976 8/1953 Bur 73421.5 X 2,682,277 6/1954 Marshall et al. 73-421.5 X 3,070,990 1/1963 Krinov 73-421.5 X 3,237,928 3/1966 Warrnan 148-165 X FREDERICK L. MATTESON, 1a., Primary Examiner.
D. A. TAMBURRO, I. J. CAMBY, Assistant Examiners.
Claims (1)
1. IN THE METHOD OF PREVENTING DEPOSITION OF CARBON FROM A HEATED CARBONACEOUS GAS, THE STEPS COMPRISING: SECURING A TUBE IN CONFLUENT RELATIONSHIP WITH A FURNACE, PROVIDING THAT PORTION OF THE TUBE HAVING A TEMPERATURE BETWEEN 1100* AND 1300*F. WITH A LINING HAVING A POSITIVE SATANDARD ELECTRODE POTENTIAL, BASED UPON THE STANDARD ELECTRODE POTENTIAL OF SODIUM AS BEING NEGATIVE, AND PASSING THE CARBONACEOUS GAS THROUGH SAID TUBE.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US437676A US3351684A (en) | 1965-03-08 | 1965-03-08 | Method of reducing carbon deposits on surfaces in contact with carbonaceous gases and subjected to elevated temperatures |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US437676A US3351684A (en) | 1965-03-08 | 1965-03-08 | Method of reducing carbon deposits on surfaces in contact with carbonaceous gases and subjected to elevated temperatures |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3351684A true US3351684A (en) | 1967-11-07 |
Family
ID=23737428
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US437676A Expired - Lifetime US3351684A (en) | 1965-03-08 | 1965-03-08 | Method of reducing carbon deposits on surfaces in contact with carbonaceous gases and subjected to elevated temperatures |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US3351684A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3947234A (en) * | 1973-08-11 | 1976-03-30 | Nippon Steel Corporation | Method of raising the temperature of reducing gas containing co component |
| US4123294A (en) * | 1977-01-28 | 1978-10-31 | General Motors Corporation | Method of separating ferritic steel or ductile iron from certain nonferrous metals |
| US4347106A (en) * | 1978-09-06 | 1982-08-31 | Dr. C. Otto & Comp. G.M.B.H | Regeneratively-operated coke oven |
Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US884181A (en) * | 1905-12-20 | 1908-04-07 | Adolph W Machlet | Case-hardening. |
| US2604936A (en) * | 1946-01-15 | 1952-07-29 | Metal Carbides Corp | Method and apparatus for controlling the generation and application of heat |
| US2648976A (en) * | 1946-04-12 | 1953-08-18 | John F Robb | Method and apparatus for gas sampling and recording analyses and temperatures |
| US2682277A (en) * | 1949-04-28 | 1954-06-29 | Standard Oil Dev Co | Apparatus for obtaining fluid samples and quenching same |
| US3070990A (en) * | 1960-02-11 | 1963-01-01 | Pittsburgh Plate Glass Co | Sampling device and method for analysis of furnace gases |
| US3237928A (en) * | 1961-12-22 | 1966-03-01 | Basic Products Corp | Control arrangement for controlled atmosphere furnace |
-
1965
- 1965-03-08 US US437676A patent/US3351684A/en not_active Expired - Lifetime
Patent Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US884181A (en) * | 1905-12-20 | 1908-04-07 | Adolph W Machlet | Case-hardening. |
| US2604936A (en) * | 1946-01-15 | 1952-07-29 | Metal Carbides Corp | Method and apparatus for controlling the generation and application of heat |
| US2648976A (en) * | 1946-04-12 | 1953-08-18 | John F Robb | Method and apparatus for gas sampling and recording analyses and temperatures |
| US2682277A (en) * | 1949-04-28 | 1954-06-29 | Standard Oil Dev Co | Apparatus for obtaining fluid samples and quenching same |
| US3070990A (en) * | 1960-02-11 | 1963-01-01 | Pittsburgh Plate Glass Co | Sampling device and method for analysis of furnace gases |
| US3237928A (en) * | 1961-12-22 | 1966-03-01 | Basic Products Corp | Control arrangement for controlled atmosphere furnace |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3947234A (en) * | 1973-08-11 | 1976-03-30 | Nippon Steel Corporation | Method of raising the temperature of reducing gas containing co component |
| US4123294A (en) * | 1977-01-28 | 1978-10-31 | General Motors Corporation | Method of separating ferritic steel or ductile iron from certain nonferrous metals |
| US4347106A (en) * | 1978-09-06 | 1982-08-31 | Dr. C. Otto & Comp. G.M.B.H | Regeneratively-operated coke oven |
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