| (19) |
 |
|
(11) |
EP 0 251 295 B1 |
| (12) |
EUROPEAN PATENT SPECIFICATION |
| (45) |
Mention of the grant of the patent: |
|
22.01.1992 Bulletin 1992/04 |
| (22) |
Date of filing: 30.06.1987 |
|
| (51) |
International Patent Classification (IPC)5: C22C 19/05 |
|
| (54) |
High nickel chromium alloy
Nickellegierung mit hohem Chromgehalt
Alliage à base de nickel, à teneur élevée en chrome
|
| (84) |
Designated Contracting States: |
|
GB |
| (30) |
Priority: |
03.07.1986 US 881623
|
| (43) |
Date of publication of application: |
|
07.01.1988 Bulletin 1988/01 |
| (73) |
Proprietor: Inco Alloys International, Inc. |
|
Huntington
West Virginia 25720 (US) |
|
| (72) |
Inventors: |
|
- Ganesan, Pasupathy
Huntington, W VA 25705 (US)
- Smith, Gaylord
Huntington, W VA 25705 (US)
- Tassen, Curtis Steven
Huntington, W VA 25705 (US)
- Wheeler, Jack Milton
Lesage, W.VA. 25537 (US)
|
| (74) |
Representative: Greenstreet, Cyril Henry et al |
|
Haseltine Lake Partners
Motorama Haus 502
Rosenheimer Strasse 30 D-81669 München D-81669 München (DE) |
| (56) |
References cited: :
SU-A- 464 648 US-A- 3 607 243
|
US-A- 3 146 136
|
|
| |
|
|
|
|
| |
|
| Note: Within nine months from the publication of the mention of the grant of the European
patent, any person may give notice to the European Patent Office of opposition to
the European patent
granted. Notice of opposition shall be filed in a written reasoned statement. It shall
not be deemed to
have been filed until the opposition fee has been paid. (Art. 99(1) European Patent
Convention).
|
[0001] The subject invention is directed to a high nickel-chromium-iron alloy, and more
particularly to a Ni-Cr-Fe alloy of special chemistry and micro-structure such that
it is capable of affording a desired combination of properties at elevated temperatures
upwards of 2000°F (1093°C) under oxidizing conditions.
[0002] Since at least the early 50's the demand has been incessant for economical materials
capable of performing satisfactorily under increasingly severe operating conditions,
notably temperature. For example, and by way of illustration, in the ceramic tile
industry frit-firing temperatures have been on the increase in an effort to accomodate
new frits and higher furnace loads, this to remain competitive in the market-place.
Initially, various manufacturers of furnace rollers for this application used an alloy
containing roughly 0.04% C, 0.25% Si, 0.25% Mn, 22.75% Cr, 0.4% Ti, 0.01% Nb, 1.35%
Al, 59.5% Ni, 0.35% Co, 0.03% N, 0.001% 0₂, balance iron, the alloy being produced
from ingots melted in an air induction furnace. The rollers lasted up to roughly 18
months at 2060°F (1127°C), ultimately failing from oxidation-enhanced stress-rupture
failure with fracture being intergranular.
[0003] More recently, the rollers have been produced from electric-arc furnace melted, argon-oxygen
decarburized (AOD) refined ingots. The composition used differed somewhat from the
above, a typical composition being approximately 0.03%C, 0.3% Si, 0.3% Mn, 22.5% Cr,
0.4% Ti, 0.02% Nb, 1.27% Al, 60.8% Ni, 0.08% Co, 0.29% Mo. 0.015% N, less than 0.001%
0₂, balance iron and impurities. At 2050°F (1121°C) rollers lasted some 12 months
and at times longer. However, at 2130°F (1165°C) such rollers manifested failure in
2 months or less.
[0004] From our investigation of the problem it would appear that failure is caused by a
rather dramatic change in microstructure as temperature is increased. This was not
initially or readily apparent since our first approach was to increase the levels
of aluminum and chromium to enhance oxidation behavior. But this was not a panacea.
In any case, extensive experimentation reflects that circa 2150°F (1177°C), and above
there is a lack of microstructural control of grain size. It would appear that the
M₂₃C₆ carbide, stabilized by silicon and molybdenum, but consisting mainly of chromium,
begins to redissolve into the matrix. This frees the grain boundaries to migrate under
applied stress and results in coarse or massive grains, e.g., one to three grains
across the wall thickness, 0.080 in. (2.0mm), of the rollers. This can be viewed,
at least in part, as failure induced by the alternating tensile and compressive stresses
set up in the rollers as a consequence of temperature and time. Actually, many grain
boundaries appear to be perpendicular to the roller surface and serve as sites for
preferential grain boundary oxidation attack which, in turn, leads to premature grain
boundary rupture.
[0005] It has now been found that the oxidation resistance of alloys of the type above-discussed
can be improved by a controlled addition and retention of nitrogen as discussed infra.
Put another way, it has been discovered that the microstructure of the alloys of the
type under consideration, notably grain size, can be controlled or rendered relatively
structurally stable over extended periods at elevated temperature through a microalloying
addition of nitrogen.
[0006] Generally speaking and in accordance with the present invention, the alloy contemplated
herein contains 19 to 28% chromium, 55 to 65% nickel, 0.75 to 2% aluminum, 0.2 to
1% titanium, from 0.1 to 1% silicon, up to 1% each of molybdenum, manganese and niobium,
up to 0.1% carbon, from 0.035 to 0.1% (e.g. 0.04 to 0.08%) nitrogen and up to 0.01%
or even 0.1% boron, up to 0.1% calcium and up to 0.1% magnesium, the balance, apart
from impurities, being iron.
[0007] A preferred alloy contains 21 to 25% Cr, 58 to 63% Ni, 1 to 2% Al, 0.3 to 0.7% Ti,
0.1 to 0.6% Si and optionally 0.1 to 0.8% Mo, up to 0.6% Mn, up to 0.4% Nb, 0.02 to
0.1% c, 0.04 to 0.08% N, with iron being the balance.
[0008] Nitrogen plays a major role in effectively enhancing oxidation resistance. It combines
with titanium to form approximately 0.15 to 0.8% of titanium nitride, depending upon
the stoichiometry of the nitride. This level of titanium nitride pins the grain size
at temperatures as high as 2192°F (1200°C). Put another way, the presence of nitrogen/nitride
increases the temperature capability over conventionally used materials by some 135°F
(75°C) or more. Below about 0.04% nitrogen (0.17% stoichiometric titanium nitride)
there would appear to be insufficient precipitate to pin the grain boundaries. Above
about 0.08% (non-stoichiometric titanium nitride) the alloy tends to become gassy,
difficult to manufacture and difficult to weld. Apart from the foregoing advantage
of this microalloy addition, stress-rupture life is increased, thus permitting furnace
operators to increase load-bearing capacity at temperature without a detrimental sacrifice
in roller life.
[0009] In carrying the invention in practice, care should be exercised in achieving proper
composition control. Nickel contributes to workability and fabricability as well as
imparting strength and other benefits. Aluminum and chromium confer oxidation resistance
but if present to the excess lend to undesirable microstructural phases such as sigma.
Little is gained with chromium levels much above 28% or aluminum levels exceeding
2%.
[0010] Carbon need not exceed 0.1% to minimize the formation of excess carbides. A level
of about 0.1 to 0.5% Cr₂₃C₆ aids strength to about 2057°F (1125°C). Silicon and molybdenum
stabilize the carbide phase. In this regard the presence of 0.1 to 0.6% silicon with
or without 0.1 to 0.8% molybdenum is advantageous.
[0011] Titanium acts as a malleabilizer as well as serving to form the grain boundary pinning
titanium nitride phase. Niobium will further stabilize the nitride phase and from
0.05 to 0.4% is beneficial.
[0012] Manganese is preferably held to low levels, preferably not about 0.6%, since higher
percentages detract from oxidation resistance. Up to 0.006% boron may be present to
aid malleability. Calcium and/or magnesium in amounts, say up to 0.05 or 0.1%, are
useful for deoxidation and malleabilization.
[0013] Iron comprises essentially the balance of the alloy composition. This allows for
the use of standard ferroalloys in melting thus reducing cost. As to other constituents,
sulphur and phosphorus present as impurities should be maintained at low levels, e.g.,
up to 0.015% sulphur and up to 0.02 or 0.03% phosphorus. Copper can be present as
an impurity.
[0014] In terms of processing, conventional air melting procedures may be used, including
the employment of induction furnaces. However, vacuum melting and refining can be
employed where desired. Preferably the alloy is electric-arc furnace melted, AOD refined
and electroslag remelted (ESR) for (a) uniform distribution of the nitrides (b) better
nitrogen content control, and (c) to maximize yield. In this connection, the nitrogen
can be added to the AOD refined melt by means of a nitrogen blow just prior to pouring
the ingot to be ESR melted. The alloy is, as a practical matter, non age-hardenable
or substantially non age-hardenable, and is comprised essentially of a stable austenitic
matrix virtually free of detrimental quantities of subversive phases. For example,
upon heating for prolonged periods, say 300 hours, at temperatures circa 1100°F (593°C)
to 1400°F (760°C) metallographic analysis did not reveal the presence of the sigma
phase.
[0015] The following information and data are given to afford those skilled in the art a
better perspective as to the nature of the alloy herein abovedescribed:
[0016] A series of alloys (Table I) were melted in an air induction furnace (Alloys C, E
and 2) or in an electric-arc furnace (Alloys A, B and D), then AOD refined and ESR
remelted. Ingots were broken down to approximately 70 mm (0.280 inch) hot bands which
were then cold rolled in coils to approximately 2 mm (0.080in) thickness with two
intermediate anneals at 2050°F (1121°C). Sheet specimens were annealed at about 2150°F
(1177°C) prior to test. A metallographic examination was then conducted upon exposing
each alloy for either 16 hour increments at 2012°F (1100°C) and 2192°F (1200°C) or
100 hour increments at 2130°F (1165°C) to measure grain growth versus time at various
temperatures. The data are reported in Table II.

[0017] Alloys A through C are low nitrogen compositions with varying carbon content. Although
increasing carbon content progressively inhibited grain growth, it was ineffective
in controlling grain size for long periods of time above about 1100°C (2010°F). Increasing
the nitrogen level resulted in several beneficial attributes, as shown by the titanium-containing
Alloy 2 of the invention. The uniform dispersion of nitride resulted in stabilization
of the grain size and longer stress rupture lives at elevated temperature. The oxidation
resistance of alloys within the invention was also improved (surprisingly) as measured
by the reduction of the denuded zone beneath the surface scale. The nitrogen levels
of Alloys D and E were also beneficial in comparison with A, B and C, but it is deemed
that Alloy D would not perform as well as Alloys E and 2 over prolonged periods, as
is indicated by the data in Table II.
[0018] Alloys A and B were fabricated into 26.9 mm diameter (1.06 in) x 2438.4mm (96 in.)
rollers using 2.0 mm (0.08 in.) gauge sheets and then field tested in an actual furnace
operating at 1165°C (2130°F). Both alloys failed by stress rupture in a short time.
Alloy C was hot worked into a solid bar 26.9 mm (1.06 in.) diameter and in field operation
for 6 days. The average grain size was 300 µm. after exposure, with grains as large
as 1500 µm. The stress rupture life of an alloy similar to alloy A at 1177°C (2150°F)
and 6.89 MPa (1 Ksi) was 308 hours.
[0019] Alloys E and 2 (and also Alloy D) were fabricated similarly and exposed to the same
thermal conditions as alloys A through C. (Alloys D, E and 2 are intermediate carbon
content compositions with increasing nitrogen levels). The beneficial effect of increasing
nitrogen content on grain size stability is demonstrated by the data in Table II.
Rollers were fabricated from Alloy 2 (and also D) as described for Alloys A and B
and are currently in field service without incident. Alloy E was fabricated into a
solid roller as described for Alloy C. This alloy (1) was tested in field service
at 1165°C (2130°F) for 8 days and then metallographically evaluated for grain size.
The grain size was 300 µm after exposure and 50 µm prior to exposure. The stress rupture
life of an alloy composition similar to Alloy 1 at 1177°C (2150°F) and 6.89 MPa (1Ksi)
was 507 hours. This increase in stress rupture life over, for example, alloy A demonstrates
a contribution to strength by the nitrogen addition. Likewise alloy D was stress rupture
tested at 1090°C (2000°F) and 13.78 MPa (2Ksi) along with an alloy similar to Alloy
C. The times to failure were a maximum of 224 and 157 hours, respectively. Again,
the contribution to strength by the nitrogen addition was noted.
[0020] In manufacturing the furnace rollers, all the above alloys were autogeneously welded
using tungsten-arc argon-shielded welding procedures. No difficulties in welding were
encountered. However, at higher than 0.08% nitrogen welding problems might ensue.
[0021] As indicated herein, electric-arc furnace melting, AOD refining with a nitrogen blow,
followed by ESR remelting of the alloy is the preferred manufacture route over air
induction furnace melting of the ingots because of improved yield to final product
and because of the better dispersion of the nitrides. An additional and unexpected
benefit of the nitrogen additions is a marked reduction of the depth of the denuded
zone (depletion of chromium and aluminum contents) as the nitrogen content is increased.
Table III shows the depth of the denuded zone for alloys C, D and 2. This dramatic
increase in resistance to alloy depletion in the base alloy is attributed to the effect
of nitrogen on grain size retention and concomitantly on oxide scale density and tenacity.
TABLE III
| EFFECT OF NITROGEN ON THE DEPTH OF THE DENUDED ZONE AFTER 600 HOURS AT 1165°C (2130°F) |
| Alloy |
Depth of Denuded Zone (µm) |
| C |
1230 |
| D |
300 |
| 2 |
150 |
[0022] Given the foregoing, including the data in Tables I, II and III it will be noted
that the subject invention provide nickel chromium alloys which afford a combination
of desirable metallurgical properties including (1) good oxidation resistance at elevated
temperatures (2) high stress-rupture lives at such temperatures, and (3) a relatively
stable microstructure. The alloys are characterized by (4) a substantially uniform
distribution of titanium nitrides (TiN) throughout the grains and grain boundaries.
The nitrides are stable in the microstructure up to near the melting point provided
at least 0.04% nitrogen is present. A nitrogen level down to 0.035% might be satisfactory
in certain instances. This is in marked contrast to the M₂₃C₆ type of carbide which
tends to go back into solution at around 2125-2150°F (1163-1177°C) whereupon nothing
remains to control grain size. It is to advantage that (5) the grain size not exceed
about 380 µm, preferably being not more than, 300 µm the size of the grains being
uniform outwardly to the alloy surface.
[0023] While the alloy of the present invention has been described in connection with the
behavior of rollers in furnaces for frit production, the alloy is also deemed useful
for heating elements, ignition tubes, radiant tubes, combustor components, burners,
heat exchangers, furnace fixtures, mufflers, belts, etc. The metal and ceramic process
industries, chemical manufactures and the petroleum and petrochemical processing industries
are illustrative of industries in which the alloy of the invention is deemed particularly
useful.
[0024] Although the present invention has been described in conjunction with preferred embodiments,
it is to be understood that it is not limited thereto.
1. A high nickel-chromium alloy characterised by (a) enhanced resistance to oxidation
at elevated temperature, (b) good stress rupture life at such temperatures, and (c)
a controlled grain size, said alloy consisting of 55 to 65% nickel, 19 to 28% chromium,
0.75 to 2% aluminum, 0.2 to 1% titanium, 0.035% to 0.1% nitrogen, up to 0.1% carbon,
from 0.1 to 1% of silicon, up to 1% each of molybdenum, manganese and niobium and
up to 0.1% boron, up to 0.1% calcium and up to 0.1% magnesium, the balance, apart
from impurities, being iron.
2. An alloy according to claim 1 containing 58 to 63% nickel, 21 to 25% chromium, 1 to
2% aluminum, 0.3 to 0.7% titanium, 0.1 to 0.6% silicon and optionally 0.1 to 0.8%
molybdenum, up to 0.6% manganese, up to 0.4% niobium, 0.02 to 0.1% carbon and 0.04
to 0.08% nitrogen.
3. An alloy according to claim 1 or claim 2 containing molybdenum.
4. An alloy according to claim 1 containing 61.17% nickel, 23.89% chromium, 1.51% aluminum,
0.37% titanium, 0.08% nitrogen, 0.04% carbon, 0.32% silicon, 0.23% molybdenum, and
0.29% manganese, the balance, apart from impurities, being iron.
5. An alloy according to any preceding claim containing at least one of calcium and magnesium.
6. A wrought article or part made from an alloy according to any preceding claim, having
a relatively stable microstructure having titanium nitrides substantially uniformly
distributed throughout the grains and grain boundaries and with the average grain
size not exceeding about 380 µm.
7. The use of an alloy according to any one of claims 1 to 5 for articles and parts requiring
good resistance to oxidation and rupture under stress for prolonged periods at temperatures
exceeding 1093°C.
8. A furnace roller formed from an alloy according to any one of claims 1 to 5.
1. Hochlegierte Nickel-Chrom-Legierung, gekennzeichnet durch (a) eine verbesserte Oxidationsbeständigkeit bei erhöhten Temperaturen, (b) gute
Zeitstandfestigkeit bei derartigen Temperaturen und (c) eingestellte Korngröße, bestehend
aus 55 bis 65% Nickel, 19 bis 28% Chrom, 0,75 bis 2% Aluminium, 0,2 bis 1% Titan,
0,035 bis 0,1% Stickstoff, bis 0,1% Kohlenstoff, 0,1 bis 1% Silizium, jeweils bis
1% Molybdän, Mangan und Niob sowie bis 0,1% Bor, bis 0,1% Kalzium und bis 0,1% Magnesium,
Rest abgesehen von Verunreinigungen Eisen.
2. Legierung nach Anspruch 1 mit 58 bis 63% Nickel, 21 bis 25% Chrom, 1 bis 2% Aluminium,
0,3 bis 0,7% Titan, 0,1 bis 0,6% Silizium und fakultativ 0,1 bis 0,8% Molybdän, bis
0,6% Mangan, bis 0,4% Niob, 0,02 bis 0,1% Kohlenstoff und 0,04 bis 0,08% Stickstoff.
3. Legierung nach Anspruch 1 oder 2 mit Molybdän.
4. Legierung nach Anspruch 1, mit 61,17% Nickel, 23,89% Chrom, 1,51% Aluminium, 0,37%
Titan, 0,08% Stickstoff, 0,04% Kohlenstoff, 0,32% Silizium, 0,23% Molybdän und 0,29%
Mangan, Rest Eisen abgesehen von Verunreinigungen.
5. Legierung nach einem der Ansprüche 1 bis 4 mit Kalzium und/oder Magnesium.
6. Gekneteter Gegenstand oder geknetetes Teil aus einer Legierung nach den Ansprüchen
1 bis 5 mit verhältnismäßig stabilem Mikrogefüge und im wesentlichen gleichmäßig über
die Gefügekörner und Korngrenzen verteilten Titannitriden sowie einer mittleren Korngröße
von höchstens etwa 380 um.
7. Verwendung einer Legierung nach einem der Ansprüche 1 bis 5 als Werkstoff für Gegenstände
und Teile mit guter Oxidationsbeständigkeit und zeitstandfestigkeit bei langfristiger
Beanspruchung über 1093°C.
8. Ofenrolle aus einer Legierung nach einem der Ansprüche 1 bis 5.
1. Alliage à haute teneur en chrome-nickel, caractérisé en ce qu'il possède (a) une meilleure
résistance à l'oxydation aux températures élevées, (b) une bonne durée avant rupture
par contrainte à de telles températures et (c) une grosseur de grain réglée, ledit
alliage consistant en 55 à 65 % de nickel, 19 à 28 % de chrome, 0,75 à 2 % d'aluminium,
0,2 à 1 % de titane, 0,035 à 0,1 % d'azote, jusqu'à 0,1 % de carbone, de 0,1 à 1 %
de silicium, jusqu'à 1 % de chacun des composants molybdène, manganèse et niobium
et jusqu'à 0,1 % de bore, jusqu'à 0,1 % de calcium et jusqu'à 0,1 % de magnésium,
le complément étant du fer, outre les impuretés usuelles.
2. Alliage selon la revendication 1, qui contient de 58 à 63 % de nickel, de 21 à 25
% de chrome, de 1 à 2 % d'aluminium, de 0,3 à 0,7 % de titane, de 0,1 à 0,6 % de silicium
et, facultativement, de 0,1 à 0,8 % de molybdène, jusqu'à 0,6 % de manganèse, jusqu'à
0,4 % de niobium, de 0,02 à 0,1 % de carbone et de 0,04 à 0,08 % d'azote.
3. Alliage selon la revendication 1 ou 2, qui contient du molybdène.
4. Alliage selon la revendication 1, qui contient 61,17 % de nickel, 23,89 % de chrome,
1,51 % d'aluminium, 0,37 % de titane, 0,08 % d'azote, 0,04 % de carbone, 0,32 % de
sillcium, 0,23 % de molybdène et 0,29 % de manganèse, le complément étant du fer outre
les impuretés usuelles.
5. Alliage selon l'une quelconque des revendications précédentes, qui contient au moins
l'un des composants calcium et magnésium.
6. Article ou pièce forgé formé à partir d'un alliage selon l'une quelconque des revendications
précédentes, comportant une microstructure relativement stable ayant des nitrures
de titane distribués d'une façon sensiblement uniforme parmi les grains et les frontières
de grains, la grosseur moyenne des grains ne dépassant pas environ 380 µm.
7. Utilisation d'un alliage selon l'une quelconque des revendications 1 à 5, pour des
articles et pièces qui exigent une bonne résistance à l'oxydation et à la rupture
sous charge pendant des périodes prolongées à plus de 1093°C.
8. Cylindre de four formé en un alliage selon l'une quelconque des revendications 1 à
5.