US3865634A - Heat resistant alloy for carburization resistance - Google Patents

Heat resistant alloy for carburization resistance Download PDF

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Publication number
US3865634A
US3865634A US387946A US38794673A US3865634A US 3865634 A US3865634 A US 3865634A US 387946 A US387946 A US 387946A US 38794673 A US38794673 A US 38794673A US 3865634 A US3865634 A US 3865634A
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United States
Prior art keywords
alloy
manganese
metal
chromium
steam
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Expired - Lifetime
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US387946A
Inventor
Donald L Bagnoli
Anthony R Ciuffreda
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
ExxonMobil Technology and Engineering Co
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Exxon Research and Engineering Co
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Publication date
Application filed by Exxon Research and Engineering Co filed Critical Exxon Research and Engineering Co
Priority to US387946A priority Critical patent/US3865634A/en
Priority to CA204,577A priority patent/CA1028601A/en
Priority to GB3143274A priority patent/GB1472090A/en
Priority to DE2434994A priority patent/DE2434994A1/en
Priority to DE19742447146 priority patent/DE2447146A1/en
Priority to NL7410570A priority patent/NL7410570A/en
Priority to FR7427906A priority patent/FR2240964B1/fr
Priority to JP49092072A priority patent/JPS5072839A/ja
Priority to BE147542A priority patent/BE818775A/en
Priority to AU72348/74A priority patent/AU484945B2/en
Priority to US501220A priority patent/US3919073A/en
Application granted granted Critical
Publication of US3865634A publication Critical patent/US3865634A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
    • C10G9/00Thermal non-catalytic cracking, in the absence of hydrogen, of hydrocarbon oils
    • C10G9/14Thermal non-catalytic cracking, in the absence of hydrogen, of hydrocarbon oils in pipes or coils with or without auxiliary means, e.g. digesters, soaking drums, expansion means
    • C10G9/18Apparatus
    • C10G9/20Tube furnaces
    • C10G9/203Tube furnaces chemical composition of the tubes
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J19/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J19/0006Controlling or regulating processes
    • B01J19/002Avoiding undesirable reactions or side-effects, e.g. avoiding explosions, or improving the yield by suppressing side-reactions
    • B01J19/0026Avoiding carbon deposits
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
    • C10G2300/00Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
    • C10G2300/40Characteristics of the process deviating from typical ways of processing
    • C10G2300/4075Limiting deterioration of equipment

Definitions

  • This invention relates to the pyrolysis of hydrocarbons. More particularly, it relates to a technique for minimizing carburization of furnace tubes exposed to hydrocarbons under pyrolysis and reforming conditions.
  • Processes for the controlled pyrolytic decomposition of hydrocarbons are well known.
  • the hydro carbon is decomposed at high temperatures, for example in the range of l,700 to 2,000 F. under varying pressure conditions ranging from atmospheric up to about 1,200 psi.
  • Such pyrolytic techniques are frequently used, for example, in producing ethylene.
  • the hydrocarbons are cracked at elevated temperatures in the presence of predetermined amounts of steam.
  • Pyrolytic techniques are also used for increasing the octane rating of gasoline.
  • a method of heating hydrocarbon carbons in contact with metal surfaces under conditions which normally would cause difficulties due to carburization of the metal surfaces which comprises contacting the hydrocarbons of the metal surface containing adherent oxide layer of manganese and chromium, whereby heat is passed from the metal surface to the hydrocarbon without significant carburization of the metal.
  • the present invention contemplates a method of rendering metal surfaces exposed to hydrocarbons under pyrolysis and reforming conditions resistant to carburization by providing on such metal surfaces in contact with the hydrocarbons and adherent layer of manganese and chromium oxide.
  • an ad herent layer of manganese and chromium oxide is formed on a metal alloy surface by oxidizing a nickelchromium-iron alloy that has at least 36% nickel and from 1.25% to 2.0% manganese.
  • the present invention can be carried out for example by passing a hydrocarbon through a heating means having one or more tubes or conduits which are heated di- 'rectly or indirectly to transfer heat to the hydrocarbon.
  • the metal surfaces to be used in accordance with this invention should have an adherent coating of manganese and chromium oxide.
  • the metal tubes are formed from an alloy consisting essentially of chromium, nickel and iron and having at least l.25% manganese and at least 36% nickel.
  • the alloy may have from 36 to 38% nickel, from 23 to 27% chromium, and from 1.25% to 2% manganese.
  • the metal surfaces are pretreated with steam at temperatures in the range of 500 F. to about 2,000 F., and preferably at about l,500 F. for from about 24 hours to about 96 hours, such as about 72 hours.
  • the grain structure of the contact surface Equally important in providing an adequate protective coating of manganese and chromium oxide on the surface of the metal is the grain structure of the contact surface. It has been discovered that with furnace tubes, for example, the interior contact surface should be made up of equiaxed grain structure. Basically the grain structure is achieved by casting the alloy into a tube and controlling the thermal gradient during solidification. Any other technique known in the art for controlling grain structure can be employed.
  • a nickel content, in a nickel-chromiumiron alloy, of greater than 36% and a manganese content of greater than 1.25% is necessary to provide a good protective scale of manganese and chromium oxide in the interior surface of the furnace tube.

Abstract

The catastrophic carburization of metal furnace tubes used in cracking and pyrolyzing hydrocarbons is minimized by forming a protective scale of manganese and chromium oxide on the surface of the metal. A nickel content of about 36 to 38% and a manganese content of 1.25 to 2.0% in a nickel-chromium-iron alloy promotes the formation of the oxide scale upon treatment of the alloy with steam.

Description

United States Patent [191 Bagnoli et a1.
[ HEAT RESISTANT ALLOY FOR CARBURIZATION RESISTANCE [75] Inventors: Donald L. Bagnoli, Oak Ridge;
Anthony R. Ciuffreda, Colonia, both of NJ.
[73] Assignee: Exxon Research and Engineering Company, Linden, NJ.
[22] Filed: Aug. 13, 1973 [21] Appl. No.: 387,946
[52] US. Cl. 148/635, 75/128 A [51] Int. Cl. C23c 13/00 [58] Field of Search 148/635; 75/128 A [56] References Cited UNITED STATES PATENTS 2,543,710 2/1951 Schmidt et a] 148/635 X [4 1 Feb. 11, 1975 3,260,594 7/1966 Ornitz et a] 75/128 A Primary ExaminerCameron K. Weiffenbach Assistant Examiner-John D. Smith Attorney, Agent, or Firm-John .1. Dvorak [57] ABSTRACT 3 Claims, No Drawings HEAT RESISTANT ALLOY FOR CARBURIZATION RESISTANCE BACKGROUND OF THE INVENTION This invention relates to the pyrolysis of hydrocarbons. More particularly, it relates to a technique for minimizing carburization of furnace tubes exposed to hydrocarbons under pyrolysis and reforming conditions.
Processes for the controlled pyrolytic decomposition of hydrocarbons are well known. Typically, the hydro carbon is decomposed at high temperatures, for example in the range of l,700 to 2,000 F. under varying pressure conditions ranging from atmospheric up to about 1,200 psi. Such pyrolytic techniques are frequently used, for example, in producing ethylene. The hydrocarbons are cracked at elevated temperatures in the presence of predetermined amounts of steam. Pyrolytic techniques are also used for increasing the octane rating of gasoline.
It has been well recognized that the abovementioned cracking and reforming processes when conducted in the presence of certain metals and metal alloys often lead to excessive deposition of carbon. These carbon deposits not only tend to reduce the size of the furnace tubes with concomitant problems of plugging, but most importantly they also affect the strength of the metal furnace tubes resulting in structural failure of the metal tubes. In such instances such failure is frequently referred to as catastrophic carburization of the metal.
It is known for example that iron surfaces will have a catalytic effect upon the pyrolysis of hydrocarbons, promoting carbon formation. The carbon formed is absorbed or diffused into metal resulting in the structural failure of into the metal. Consequently, numerous techniques have been proposed for avoiding such catastrophic carburization of metal tubes by alloying the iron and/or by forming protective coatings of an oxide on the surface of the metal to be contacted with the hydrocarbon under the reforming or pyrolysis conditions. None of these techniques have provided a complete panacea and there is more than definite commercial interest in prevent carburization of furnace tubes exposed to hydrocarbons under pyrolysis and reforming conditions.
SUMMARY OF THE INVENTION According to the present invention, there is provided a method of heating hydrocarbon carbons in contact with metal surfaces under conditions which normally would cause difficulties due to carburization of the metal surfaces which comprises contacting the hydrocarbons of the metal surface containing adherent oxide layer of manganese and chromium, whereby heat is passed from the metal surface to the hydrocarbon without significant carburization of the metal.
Thus, in one aspect the present invention contemplates a method of rendering metal surfaces exposed to hydrocarbons under pyrolysis and reforming conditions resistant to carburization by providing on such metal surfaces in contact with the hydrocarbons and adherent layer of manganese and chromium oxide.
In yet another aspect of the present invention, an ad herent layer of manganese and chromium oxide is formed on a metal alloy surface by oxidizing a nickelchromium-iron alloy that has at least 36% nickel and from 1.25% to 2.0% manganese.
DETAILED DESCRIPTION OF THE INVENTION The present invention can be carried out for example by passing a hydrocarbon through a heating means having one or more tubes or conduits which are heated di- 'rectly or indirectly to transfer heat to the hydrocarbon. The metal surfaces to be used in accordance with this invention should have an adherent coating of manganese and chromium oxide.
In a particularly preferred embodiment of the present invention the metal tubes are formed from an alloy consisting essentially of chromium, nickel and iron and having at least l.25% manganese and at least 36% nickel. For example, the alloy may have from 36 to 38% nickel, from 23 to 27% chromium, and from 1.25% to 2% manganese. Indeed such an alloy when contacted with steam at elevated temperatures for a time sufficient to oxidize some of the manganese present in the alloy results in the formation of an adherent protective coating of manganese and chromium oxide which is resistant to carburization. For example, the metal surfaces are pretreated with steam at temperatures in the range of 500 F. to about 2,000 F., and preferably at about l,500 F. for from about 24 hours to about 96 hours, such as about 72 hours.
Equally important in providing an adequate protective coating of manganese and chromium oxide on the surface of the metal is the grain structure of the contact surface. It has been discovered that with furnace tubes, for example, the interior contact surface should be made up of equiaxed grain structure. Basically the grain structure is achieved by casting the alloy into a tube and controlling the thermal gradient during solidification. Any other technique known in the art for controlling grain structure can be employed.
The invention will be better understood by reference to the following examples and demonstrations.
EXAMPLE 1 TABLE I Alloy 1 Alloy 2 Carbon, 0.4-0.5 0.43 Manganese, 7r l.09 1.30 Silicon, L01 L10 Chromium, 7: 28.0 23.5 Nickel, 70 19.0 37.0 Molybdenum, 7c 0 L89 Iron, Balance Balance At the end of 30,000 hours on stream the furnace tubes were physically inspected. Those tubes of alloy l were, at least in some instances, carburized as much as and had as little as two-thirds of an effective wall thickness remaining. Those of alloy 2 were effectively protected against carburization. Magnetic readings of the tubes of both alloy 1 and alloy 2 showed that the protected regions were predominantly oxides of manganese and chromium whereas the unprotected areas were predominantly oxides of iron.
in a more detailed analysis performed with a microprobe analyzer, it was surprisingly discovered that a continuous layer of manganese oxide was lying outside the chromium oxide layer and close to the surface and the highly protected layers. Indeed, in alloy 2 the thickness of the manganese oxide scale was about times greater than the amount of manganese oxide scale in alloy 1.
Apparently, a nickel content, in a nickel-chromiumiron alloy, of greater than 36% and a manganese content of greater than 1.25% is necessary to provide a good protective scale of manganese and chromium oxide in the interior surface of the furnace tube.
Although the present invention has been described in conjunction with preferred embodiments, it is to be understood that modifications or variations may be resorted to without departing from the spirit and scope of the invention. Those skilled in the art will readily understand that such modifications and variations are considered to be within the purview and scope of the invention and appended claims.
What is claimed is: l. The method of forming a protective scale of manganese and chromium oxide on the surface of alloy consisting essentially of manganese, chromium, iron and nickel comprising: 7
l. adjusting the nickel content of the alloy to the range of 36 to 38% and the manganese content of the alloy from 1.2 to 2.0%;
2. forming the alloy'into a metal surface; and
3. thereafter, treating the metal surface with steam at elevated temperatures for a time sufficient to oxidize manganese and chromium present in the alloy and form a protective scale of manganese and chromium oxide.
2. The method of claim 1 wherein the metal is treated with steam at temperatures in the range of 500 F. to 2,000 F. for at least about 24 hours.
3. The method of claim 1 wherein the metal is treated with steam at a temperature of about l,450 F. for
about 72 hours.

Claims (8)

1. THE METHOD OF FORMING A PROTECTIVE SCALE OF MANGANESE AND CHROMIUM OXIDE ON THE SURFACE OF ALLOY CONSISTING ESSENTIALLY OF MANGANESE, CHROMINUM, IRON AND NICKEL COMPRISING:
1. ADJUSTING THE NICKEL CONTENT OF THE ALLOY TO THE RANGE OF 36 TO 38% AND THE MANGANESE CONTENT OF THE ALLOY FROM 1.2 TO 2.0%,
2. FORMING THE ALLOY INTO A METAL SURFACE, AND
2. forming the alloy into a metal surface; and
2. The method of claim 1 wherein the metal is treated with steam at temperatures in the range of 500* F. to 2,000* F. for at least about 24 hours.
3. The method of claim 1 wherein the metal is treated with steam at a temperature of about 1,450* F. for about 72 hours.
3. thereafter, treating the metal surface with steam at elevated temperatures for a time sufficient to oxidize manganese and chromium present in the alloy and form a protective scale of manganese and chromium oxide.
3. THERAFTER, TREATING THE METAL SURFACE WITH STEAM AT ELEVATED TEMPERATURES FOR A TIME SUFFICIENT TO OXIDIZE MANGANESE AND CHROMIUM PRESENT IN THE ALLOY AND FORM A PROTECTIVE SCALE OF MANAGANESE AND CHROMIUM OXIDE.
US387946A 1973-08-13 1973-08-13 Heat resistant alloy for carburization resistance Expired - Lifetime US3865634A (en)

Priority Applications (11)

Application Number Priority Date Filing Date Title
US387946A US3865634A (en) 1973-08-13 1973-08-13 Heat resistant alloy for carburization resistance
CA204,577A CA1028601A (en) 1973-08-13 1974-07-11 Heat resistant alloy for carburization resistance
GB3143274A GB1472090A (en) 1973-08-13 1974-07-16 Heat resistant alloy forcarburization resistance
DE2434994A DE2434994A1 (en) 1973-08-13 1974-07-20 PROCESS FOR HEATING HYDROCARBONS IN THE PRESENT NICKEL-IRON METAL SURFACES
DE19742447146 DE2447146A1 (en) 1973-08-13 1974-07-20 PROCESS FOR THE FORMATION OF A PROTECTIVE LAYER FROM MANGANIUM AND CHROMOXYDE
NL7410570A NL7410570A (en) 1973-08-13 1974-08-06 PROCEDURE FOR ANTI-CARBONATION OF OVEN TUBES IN PYROLYSIS AND REFORMING OF HYDROCARBONS.
FR7427906A FR2240964B1 (en) 1973-08-13 1974-08-12
JP49092072A JPS5072839A (en) 1973-08-13 1974-08-13
BE147542A BE818775A (en) 1973-08-13 1974-08-13 PROCESS FOR HEATING HYDROCARBONS
AU72348/74A AU484945B2 (en) 1973-08-13 1974-08-14 Heat resistant alloy for carburization resistance
US501220A US3919073A (en) 1973-08-13 1974-08-28 Heat resistant alloy for carburization resistance

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US387946A US3865634A (en) 1973-08-13 1973-08-13 Heat resistant alloy for carburization resistance

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US3865634A true US3865634A (en) 1975-02-11

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US (1) US3865634A (en)
JP (1) JPS5072839A (en)
BE (1) BE818775A (en)
CA (1) CA1028601A (en)
DE (2) DE2447146A1 (en)
FR (1) FR2240964B1 (en)
GB (1) GB1472090A (en)
NL (1) NL7410570A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4784831A (en) * 1984-11-13 1988-11-15 Inco Alloys International, Inc. Hiscor alloy
US5169515A (en) * 1989-06-30 1992-12-08 Shell Oil Company Process and article
US5873950A (en) * 1996-06-13 1999-02-23 Inco Alloys International, Inc. Strengthenable ethylene pyrolysis alloy

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5684789A (en) * 1979-12-13 1981-07-10 Toyo Eng Corp High-temperature treatment of hydrocarbon-containing material
GB2233672A (en) * 1989-06-30 1991-01-16 Shell Int Research High temperature treatment of stainless steals used in high temperature reactors
DE10017512A1 (en) * 2000-04-10 2001-10-18 Atec Weiss Gmbh & Co Kg Ring plate for flexible shaft couplings, plate pack formed from such ring plates and flexible shaft coupling with such ring plates
US6824883B1 (en) * 2000-09-12 2004-11-30 Nova Chemicals (International) S.A. Surface on a stainless steel matrix
US6899966B2 (en) 2003-06-24 2005-05-31 Nova Chemicals (International) S.A. Composite surface on a stainless steel matrix
FR3060430B1 (en) * 2016-12-20 2019-07-19 Institut National Des Sciences Appliquees De Lyon (Insa Lyon) METHOD FOR THE MECHANICAL TREATMENT OF A WALL REDUCING COKE FORMATION.

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2543710A (en) * 1948-01-15 1951-02-27 Westinghouse Electric Corp Process for producing insulating iron oxide coatings
US3260594A (en) * 1965-01-11 1966-07-12 Blaw Knox Co High temperature alloys

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2543710A (en) * 1948-01-15 1951-02-27 Westinghouse Electric Corp Process for producing insulating iron oxide coatings
US3260594A (en) * 1965-01-11 1966-07-12 Blaw Knox Co High temperature alloys

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4784831A (en) * 1984-11-13 1988-11-15 Inco Alloys International, Inc. Hiscor alloy
US5169515A (en) * 1989-06-30 1992-12-08 Shell Oil Company Process and article
US5873950A (en) * 1996-06-13 1999-02-23 Inco Alloys International, Inc. Strengthenable ethylene pyrolysis alloy

Also Published As

Publication number Publication date
DE2434994A1 (en) 1975-02-20
FR2240964B1 (en) 1978-07-13
GB1472090A (en) 1977-04-27
CA1028601A (en) 1978-03-28
FR2240964A1 (en) 1975-03-14
NL7410570A (en) 1975-02-17
DE2447146A1 (en) 1975-06-26
AU7234874A (en) 1976-02-19
BE818775A (en) 1975-02-13
JPS5072839A (en) 1975-06-16

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