Metal treatment – Process of modifying or maintaining internal physical... – With casting or solidifying from melt
Reexamination Certificate
2000-09-26
2003-04-08
Wyszomierski, George (Department: 1742)
Metal treatment
Process of modifying or maintaining internal physical...
With casting or solidifying from melt
C148S612000, C148S614000, C164S004100, C164S057100
Reexamination Certificate
active
06544359
ABSTRACT:
CROSS REFERENCE TO RELATED APPLICATION
The present application is the national stage under 35 U.S.C. 371 of PCT/SE99/00456, filed Mar. 23, 1999.
INTRODUCTION
Cast irons can be divided into four major groups, flake graphite, malleable, spheroidal and compacted graphite iron (CGI) as described in Cast Iron Technology by Roy Elliott, Butterworths 1988 and in ASM Specialty Handbook, Cast Iron, edited by J. R. Davis, Davis & Associates 1996, the disclosures of which are herewith incorporated by reference. In malleable iron graphite phase is formed as a result of a solid state reaction, but in the other kinds of iron, graphite is precipitated out of the liquid during solidification. Depending on nucleating particles present in the melt and on the prevailing constitutional conditions (i.e. the presence of certain alloying elements and impurities) the various forms of graphite crystals are growing from the melt, as flakes, nodules or compacted (vermicular) crystals. Cast iron with various forms of graphite exhibits different mechanical and physical properties. Cast iron with compacted graphite, defined as Type IV in ASTM A 247 is characterised by high strength, reasonable ductility, good heat conductivity and high damping capacity, which makes the material especially interesting for production of engine blocks, cylinder heads, exhaust manifolds, disk breaks and similar products for the automotive industry. The material is, however, rather difficult to produce as it requires specific nuclei and a very narrow control of elements like sulphur and oxygen. The present invention describes a method by which these requirements can be fulfilled during a foundry production process.
First a review of different kinds of nucleating particles is presented:
Flake Graphite
Normally nucleating particles consist of saturated SiO
2
(cristobalite or tridymite) which are formed at high silicon and oxygen contents, the reaction of Si to SiO
2
occurs within the normal casting temperature range and there is a good lattice fit (epitaxy) between the graphite crystals and cristobalite. The formation of SiO
2
particles may, by kinetic reasons, be facilitated by the presence of stable oxide particles like Al
2
O
3
.
Compacted Graphite Iron (CGI)
It has been found that in compacted graphite iron SiO
2
particles are not very efficient as nucleating particles but so are various forms of magnesium silicates. In cases where SiO
2
is present there is a great risk that graphite flakes nucleate, which is disastrous for the compacted graphite iron quality. The silicate particles are, however, good nucleants for the compacted graphite crystals which will develop in full provided the remaining oxygen content, after magnesium-treatment of the melt, is kept in a suitable range normally between 20 to 60 ppm.
Nodular Iron
It is not quite clear what kind of nucleating particles are the most efficient in triggering the growth of nodular graphite particles, which, due to heavy desoxidization, to a remaining oxygen concentration between 5 and 10 ppm, develop in a nodular form.
It is obvious from above, that in gray cast iron and in compacted graphite iron, nucleant particles consist of desoxidization products, in gray iron preferentially silica (SiO
2
) and in compacted graphite iron, after the addition of magnesium, of magnesium silicate particles. These latter particles need a larger degree of undercoooling before they become active as nuclei.
BACKGROUND OF THE INVENTION
The relative amount of silicate particles formed at the addition of magnesium at the start of the deoxidization process depends on the amount of oxygen originally present in the melt. A control of the oxygen content (dissolved oxygen) is therefore of great importance in production of compacted graphite iron. There are several means to assess the oxygen content, from direct EMF (electromotive force) based measurements to indirect methods based on thermal analysis. Such methods are known to the man skilled in the art. It must be noted, however, that direct measurements and determination of oxygen content in samples extracted under vacuum show lower results than samples poured into a sample mould, where oxygen may be absorbed from the air and from the mould material.
In liquid iron, certain reactions arc of specific importance in determining the thermodynamic conditions. First, the reduction temperature of SiO
2
by carbon:
SiO
2
+2C⇄Si+2 CO I
This temperature may be referred to as the “boiling temperature” (TB) where bubbles appear as the CO-gas is expelled. This temperature is usually 50 to 100° C. above the “equilibrium temperature” (TE) at which further pick up of oxygen leads to formation of saturated SiO
2
:
TE
=
27486
15
,
47
-
log
⁢
⁢
(
Si
C
2
)
-
273
,
15
⁢
[
°
⁢
⁢
C
.
]
II
The relation between these two temperatures is given by:
TB=0.7866 TE+362 III
expressing the displacement of the “boiling point”. The temperature interval between TE and TB depends on the carbon and silicon content of the melt, but is commonly found between 1400° and 1500° C. In this temperature region, oxygen can readily be picked up, absorbed, by the melt. The absorption rate of oxygen, up to the point where FeO is formed, depends on the temperature difference between the actual temperature of the mel (TM) and TE. The absorption follows an exponential function. The temperature at which the melt is poured into the moulds is usually adjusted to values between TE and TB, the higher the thinner the sections in the casting of compacted graphite iron are.
In the case of producing CGI, an addition of silicon is required followed by deoxidation with magnesium. In order to calculate the amount of deoxidizing addition needed to produce CGI, the oxygen potential of the melt must be known precisely. This can be determined by calculations, calibration or by a direct or indirect measurement of the oxygen content by methods known per se.
The aim of the desoxidazation process is two-fold:
a) to precipitate Mg/Fe-silicate particles which constitute good nucleating sites for compacted—graphite crystals, and
b) to reduce the oxygen content of the melt to the desired level, before pouring the melt into moulds.
Unless the process is controlled within very narrow limits, there is a great risk that flake crystals or an excess of nodular crystals appear in the casting. In the following these limits are specified.
DISCLOSURE OF THE INVENTION
Thus, the present invention relates to a method of producing objects of cast iron containing compacted (vermicular) graphite by:
a) preparing a cast iron melt, preferably with the same requirements regarding base material as is common practice for the production of ductile iron, having substantially a carbon content at the desired final level and a silicon content below the desired final value, so that the equilibrium temperature (TE) for the reaction between carbon and SiO
2
, falls near 1400° C.;
b) adjusting the temperature of the melt (TM) to a value between the equilibrium temperature (TE) and the “boiling temperature” (TB), at which carbon monoxide (CO) is expelled from the melt, to allow absorption of oxygen by the melt to a level exceeding the desired level at the time the melt is poured into a mould, preferably to above a concentration of 50-100 ppm, adding a required amount of silicon and thereafter reducing the oxygen content by addition of magnesium or a magnesium containing material, preferably an FeSiMg-alloy to an oxygen level of 10 to 20 ppm oxygen in liquid solution, and forming, during the reduction process, particles of magnesium containing silicates.
The melt temperature (TM) may be adjusted during the absorption of oxygen to a value of at least 20° C. above TE and at most 10° C. below TB.
The addition of deoxidizing agent is preferably calculated to result in a casting containing more than 80% of compacted graphite crystals, the remainder being nodular crystals and practically no graphite flakes, in wall sections between 3 and 10 mm.
The oxygen content is suita
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