[0001] In the metal casting industry, it is customary to employ metal casting vessels,
such as tundishes and ladles, etc., as means which serve to transfer various molten
metals. Because of the corrosive nature of the liquid metals and the slags, and to
prevent heat loss and premature solidification of the metals, the metal casting vessels
are prevented from contacting with such metals and/or slags by lining the vessels
with heat-insulating refractory boards. Additionally, a trend in the industry is to
preheat these lined vessels to minimize heat loss from the initial molten metals poured
through the vessels at the start of casting, and to remove, if possible, all sources
of hydrogen derived from, for instance, moisture (H₂O) and/or organic compounds embodied
in the refractory linings, which can be dissolved by and incorporated into the liquid
metals passing through the lined vessels. In particular, when low hydrogen grades
of steel are being cast, it is especially desirable to preheat such refractory lined
vessels to remove all possible hydrogen sources which can serve only to contaminate
the liquid metals.
[0002] In addition to driving off all sources of hydrogen, it is desirable to minimize the
amount of unstable oxides, such as silica, which are present in the heat-insulating
refractory boards. These unstable oxides, and in particular silica, can react with
various elements contained in the molten metals and lead to the formation of oxide
inclusions in the liquid metals. For example, some of the undesirable reactions of
silica with various elements leading to the formation of oxide impurities are as follows:
SiO₂ + [2Mn] 2MnO + [Si]
3SiO₂ + [4Al] 2Al₂O₃ + [Si]
SiO₂ + [2Fe] 2FeO + [Si]
[0003] The MnO and FeO formed can further attack the silica in the heat-insulating refractory
linings by forming low melting liquid oxide slags at metal casting temperatures.
[0004] Unfortunately, the dilemma facing the metal-making industry concerning the addition
of unstable oxides which act to lower sintering and solidus temperature versus the
use of pure, stable refractory oxides for refractoriness and molten metal purity is
extremely difficult to overcome, especially with preheatable heat-insulating refractory
boards which must sinter and develop sufficient hot strength for casting at sub-casting
temperatures which can be sometimes as much as about 1,000°F. lower than casting temperatures.
[0005] Another problem presently associated with the heat-insulating refractory linings
for the metal casting vessels involves shrinkage of such linings upon heating. One
solution within the metal-making industry to this problem is to fire such linings
at temperatures higher than those that are expected during use, so that shrinkage
during use can be avoided. Again, since preheating can occur at temperatures as low
as about 1000°F. below casting, this presents a further problem with the current preheatable
boards.
[0006] In this case of cold tundish practice, i.e., the pouring of a molten metal into a
tundish without first preheating it, the temperature increases as the molten metal
enters the tundish and decomposes the organic binder under reducing conditons forming
carbon bonds. The carbon bonds hold the refractory grain together giving the tundish
lining the required hot strength. As the carbon bonds are dissolved by the molten
metal and oxidized, sintering of the refractory grain occurs over time. Thus, in cold
tundish practice, the organic binder decomposition gives carbon bonds allowing the
use of more stable refractory oxides which sinter more slowly and at higher temperatures,
i.e., MgO and silica.
[0007] Nevertheless, in casting, the temperature associated with cold tundish linings increases
quickly to that of casting such that by the time the carbon bonds are completely disintegrated,
the linings are still held together by the formation of ceramic bonds resulting from
the sintering of the refractory oxides. Because preheating may sometimes last up to,
for example, 12 hours before casting actually begins, the linings utilized in cold
tundish practice are unsuited for preheating use. The problem basically is due to
oxidation of the carbon bonds within the linings at preheat temperatures which are
generally too low for ceramic bonds to form resulting in usually soft and weak linings
which will collapse due to their own weight or wash away as the molten metal enters
the vessels.
[0008] In the past, several attempts or approaches without success have been made to overcome
the problems presently associated with preheatable heat-insulating refractory boards
for metal casting vessels. For example, large amounts of low-melting glass formers,
such as borax, have been incorporated into the linings in an effort to stick the refractory
grain together at preheat temperatures. Unfortunately, the glassy or liquid bonds
allow the preheated linings to be deformed easily at preheat and casting temperatures
after the carbon bonds burn out. Further, the preheated linings generally fail to
develop the requisite hot strength casting when preheated at preheat temperatures
for extended periods of time prior to the start of casting. As a result, it has generally
been found that at both preheat and casting temperatures, the liners would collapse
or wash away.
[0009] An additional problem associated with the use of low-melting glass formers is that
they are generally thermodynamically unstable to, for instance, ferrous alloys. In
the case of B₂O₃, it can be reduced resulting in the incorporation of boron into the
molten metals, such as ferrous alloys, that can alter the properties of the ferrous
alloys as well as product oxide inclusions.
[0010] Other types of preheatable linings are those made with the addition of about 5% to
about 20% quartz (silica) for the purpose of bonding with MgO. Unfortunately, these
preheatable boards have two serious drawbacks. First, the addition of quartz or other
silica forms utilized by these liners is sufficiently high enough to cause formation
of oxide inclusions by reaction of the molten metals with the linings. In order to
minimize liquid metal contamination, the metal manufacturers specify that the quartz
or free silica levels should be as low as possible. Secondly, presence of finely divided
quartz or free crystalline silica can become airborne when, for instance, the boards
are removed from the vessels after use presenting health hazards to the metal manufacturers
and workers.
[0011] Examples of still other types of preheatable linings are those which contain about
85-90% magnesite and about 5% to about 10% calcium fluoride. The calcium fluoride
is typical of a strong fluxing agent which reacts with oxides to develop a liquid
bonding phase at preheat temperatures. These linings, like those utilizing the low-melting
glass formers, develop a liquid bonding phase when the organic binder is burnt out
at, for instance, 1900°F. and up (preheat temperatures). The linings, unfortunately,
are also very soft and weak at such temperatures after the organic binder is oxidized.
Thus, as with the preheatable linings containing low melting glass formers, these
preheatable linings fail to develop the sufficient hot strength for casting when
heated at preheat temperatures for typical preheat periods of time.
[0012] In summary, previous attempts or approaches have been made to develop suitable preheatable
insulating refractory liners. Heretofore no satisfactory preheatable heat-insulating
refractory liner has been developed which can overcome the problems aforementioned.
Basically, the past preheatable liners fall into two categories: those in which quartz
is added in unacceptable amounts to form a ceramic bond; and those in which low melting
materials are added to develop a liquid phase at preheat temperatures as an unsatisfactory
attempt to protect the carbon bonds from oxidation and to bond the refractory grain
and promote sintering.
[0013] In other words, all of the preheatable heat-insulating refractory liners provided
hitherto invariably necessarily lack some of the key fundamental qualities required
to develop sufficient hot strength at preheatable or sub-casting temperatures for
the typical range in which preheating times occur. Consequently, there are strong
commercial needs for preheatable heat-insulating refractory liners for metal casting
vessels that can initiate the development of hot strength at preheat temperatures,
that can withstand preheat temperatures for extended periods of preheat time, that
can withstand molten metal erosion and corrosion, that will not experience substantial
shrinkage on use, and that has minimum amounts of free silica and hydrogen content.
[0014] In brief, the present invention seeks to alleviate the above-mentioned problems and
shortcomings of the present state of the art through the discovery of novel preheatable
molded refractory insulating liners and methods of use thereof for lining metal casting
vessels intended to contain, for instance, ferrous alloys, such as steel and in particular
low hydrogen grades of steel.
[0015] A method of making a preheatable molded refractory insulating liner of predetermined
shape which assists in the solution of these problems, in accordance with the invention,
comprises making a preheatable molded refractory insulating liner structure of predetermined
shape having insulating porosity for temporarily lining a casting vessel and for developing
sufficient hot strength to maintain the integrity of the structure at vessel preheat
and metal casting temperatures which are in the range of about 1900°F. to about 3000°F.
during its use as a liner in a casting vessel,comprising making a molded uniform mixture
having a substantial insulating porosity on the order of about 50% prior to preheating
containing a particulate refractory component in an amount of about 75% to about 98.5%
by weight of said preheatable liner structure of a mixture of zircon and MgO refractory
grain wherein said zircon and MgO refractory grain are in a ratio of about 1:1.5 to
about 1:24, respectively, and adding a binder for said component and inorganic fibrous
material in sufficient amounts to maintain the predetermined shape of insulating porosity
at least prior to the preheat temperatures wherein said zircon and MgO refractory
grain are of a particle size in said preheatable liner structure to facilitate the
formation of fosterite bonding which results in increased hot strength with substantial
maintenance of insulating porosity and shape without substantial shrinkage at both
the vessel preheat temperatures of about 1900°F to about 2400°F and higher metal casting
temperatures when said preheatable liner structure is used as a liner in a casting
vessel and heated for a sufficient period of time. One embodiment of a liner resulting
from this method is a preheatable molded refractory insulating liner for a casting
vessel suitable for developing sufficient hot strength at vessel preheat and metal
casting temperatures which are in the range of about 1900°F. to about 3000°F. comprising
a liner structure of predetermined shape, the liner structure comprising a molded
uniform mixture containing a particulate refractory component comprised of zircon
and MgO refractory grain and a binder for the component to maintain the predetermined
shape at least prior to the preheat temperatures wherein the zircon and MgO refractory
grain are in amounts proportioned in the liner structure to facilitate the formation
of fosterite bonding which results in increased hot strength at vessel preheat and
metal casting temperatures when such a liner structure is heated for a sufficient
period of time. Typically, in the industry preheat times can be from about one half-hour
and extend to about twelve hours or more. Preferably, the MgO refractory grain may
be derived from, for instance, natural, seawater or brine magnesite, periclase grain,
or other suitable sources, or mixtures thereof plus, if any, incidental impurities.
The MgO refractory grain and the zircon are the main essential constituents responsible
for the development of the hot strength at the vessel preheat and metal casting temperatures.
At such temperatures, it is believed that the MgO refractory grain and zircon react
as follows to form the fosterite bonds and zirconia needed for hot strength and refractoriness:
2MgO + ZrO₂ SiO₄ Mg₂SiO₄ + ZrO₂
It is thought that the formation of zirconia and fosterite enhances the desirable
hot strength and corrosion resistance to the molten metals, such as ferrous alloys,
and slag. It should be appreciated, however, that the formation of fosterite and zirconia
is believed to occur over the entire range of vessel preheat and metal casting temperatures
which are on the order of about 1900°F. to about 3000°F. More particularly, the vessel
preheat temperatures, for instance, can range from, for example, about 1900°F. to
about 2400°F. whereas, in the case of ferrous alloys, the metal casting temperatures
are generally at about 2800°F. or above.
[0016] In a further feature of this invention, the particulate refractory component may
contain in addition to the zircon and MgO refractory grain a suitable refractory filler
in acceptable amounts, such as olivine or zirconia.
[0017] Therefore, the new and vastly improved preheatable liner structures provide means
for developing effectively the increased hot strength needed for casting molten metals
at both vessel preheat and metal casting temperatures. Further, the unique preheatable
liners possess the necessary hot strength during the range of casting temperatures
that are experienced in the metal making industry and especially the ferrous alloy
making industries. In effect, a feature of the present invention is to provide preheatable
molded refractory insulating liners that possess corrosion-erosion resistance to metal
making environments which is greatly superior to that of the common commercial preheatable
refractories used heretofore. Thus, the present invention provides a solution to the
art that has long sought suitable liners for preheating and makes it now possible
to make preheatable casting vessels lined with the preheatable refractory insulating
liners of this invention for extended periods of time prior to the start of casting.
Further, it is found that extended preheating advantageously enhances the development
of the desired increased hot strength in the liners of the present invention.
[0018] Magnesite and zircon refractory compositions for fabricating refractory bricks having
utility incident to the glass and metal making industries have been heretofore known
in the art. Examples of refractory bricks formulated from such compositions can be
found in U.S. Patent No. 3,303,032, U.S. Patent No. 3,192,059 and U.S. Patent No.
3,528,830. It also has been heretofore known, as described in U.S. Patent No. 3,303,032,
that mixtures of stabilized zirconia, fosterite and periclase have resulted only after
prolonged firing of such bricks at temperatures generally far in excess of those encountered
at low vessel preheat temperatures.
[0019] In the literature, it has been reported that the decomposition of zircon to produce
zirconia and amorphous silica generally occurs at about 1600°C. (2980°F.). Zirconia
silicate (Zircon). IN: Ryshkewitch, E. (Ed); Oxide Ceramics. Academic Press pp. 399-406
(1960). In addition, it has been reported that basic substances such as MgO decompose
zircon at about 1240°C. (2264°F.). W. Eitel, "Silica Melt Equilibria", Rutgers University
Press, New Brunswick, N.J. p. 17 (1951). This agrees with R. F. Rea,
J. Am. Cermic Soc., 22, 95 (1929) who reported MgO to be among several oxides which react with zircon
to form melting slag mixtures. Thus, the early literature and U.S. Patents teach that
zircon is decomposed by MgO at about 2264°F. and develops a fosterite matrix only
after prolonged firing at temperatures generally far in excess of the usual low vessel
preheat temperatures associated with the preheatable liners presently available.
[0020] Recently, S. Yangyun and R. J. Brook: Preparation and Strength of fosterite - Zirconia
Ceramic Composites.
Ceramics International. 9(2):39-45 (1983) described the reaction of magnesium oxide (MgO) with zircon (ZrO₂
SiO₂) as follows:
2MgO + ZrO₂ SiO₂ 2MgO SiO₂ + ZrO₂. The authors therein used a low temperature
calcined reactive fine grain MgO intimately mixed with finely milled zircon. The reactants
were milled together in a micronizer and pressed into pellets. They reported that
about 10% reaction was achieved at 1100°C. (2012°F.) in two hours.
[0021] Notwithstanding the fact that such teachings as to zircon and MgO refractory compositions
have been well known in the glass and metal making industries, it has been heretofore
unknown to utilize zircon and MgO refractory compositions to form fosterite at low
vessel preheat temperatures. Further, it has been heretofore unknown to utilize such
compositions to fabricate preheatable molded refractory insulating liner structures
for casting vessels. Moreover, it has been surprisingly discovered that such compositions
in the liners react to facilitate development of effective hot strength at low vessel
preheat temperatures.
[0022] To improve the quality of the molten metals including ferrous alloys, and especially
low hydrogen grades of steel, during casting, the heat-insulating refractories employed
to line the casting vessels which come into contact with the molten metals should
be composed of the most stable oxides possible (i.e., the stronger the chemical bonding
of the oxides, the higher the melting point). Unfortunately, this means that temperatures
greater than preheatable temperatures which are generally from about 1900°F. to about
2400°F. are required to sinter the refractory grain of the stable oxides present in
the linings. Thusly, a balance or compromise has to be struck between the refractory
stable oxides and impurities utilized in the present heat-insulating refractory boards.
The refractory stable oxides must have enough impurities, but without sacrificing
quality of the casting metals, to develop a dense sinter surface at temperatures of
about 2800°F. or higher. The types and amounts of unstable impurities which act to
lower temperatures needed for sintering and solidus, however, must be controlled to
maintain the needed heat-insulating refractory lining requirements and to minimize
the contamination of the casting metals by the unstable oxides. The present invention,
however, has remarkably overcome this arduous dilemma by providing a unique blend
of stable and unstable oxides which is suitable for developing the necessary refractoriness
and hot strength at vessel preheat and casting temperatures while developing a dense
sinter at about 2800°F. without significantly contaminating the molten metals, such
as ferrous alloys, with impurities during casting.
[0023] In a further feature of the present invention, the binder component may be derived
from organic and/or inorganic binders or mixtures thereof in the range from about
1.5% to about 15% by weight. The inorganic binder may, for instance, constitute low
melting fluxing compounds, such as boric acid. Additionally, the preheatable liners
may contain a fibrous material component which may also be derived from organic and/or
inorganic materials in the range from 0% to about 10% by weight. In keeping with the
invention, the preheatable liner may further contain a thioxotropic substance, such
as bentonite, in amounts ranging from 0% to about 5% by weight.
[0024] In still a further feature of the present invention resides in providing preheatable
molded refractory insulating liner structures suitable for lining casting vessels
like hot tops, ladles, tundishes, troughs, or pipes, etc. for conveying molten ferrous
alloys. The preheatable liners, if desired, can be molded into the form of a plurality
of predetermined shaped inserts, such as tundish boards.
[0025] An especially desirable corrosion-erosion resistant preheatable molded refractory
insulating liner according to this invention comprises by weight about 80% to about
95% a particulate refractory component containing MgO refractory grain and zircon
wherein the MgO refractory grain and zircon are in a ratio of about 5:1 to about 18:1,
respectively, about 1% to about 8% fibrous material, about 1.5% to about 10% binder,
and about 0.5% to about 5% a thixotropic substance. As noted above, the MgO refractory
grain may be derived from, for instance, natural, seawater or brine magnesite, periclase
grain, or other suitable sources, or mixtures thereof. The lower silica and hydrogen
content of the preheatable structures provide a further feature for reasons recited
above; that is, the cast molten metals and particularly the ferrous alloys are distinctly
purer as a result of less contamination presently experienced from high silica and
hydrogen content associated with the common preheatable refractories available hitherto.
[0026] A preferred form of liner resulting from the present invention and possessing the
high degree of hot strength developed at vessel preheat and metal casting temperatures
comprising by weight about 10% zircon and about 80% MgO refractory grain plus incidental
impurities, wherein the MgO is preferably derived from dead burned natural, seawater
or brine magnesite, periclase grain or mixtures thereof which may range from about
80% to about 98% MgO purity, the balance being binder, and if desired fibrous material
or bentonite or mixtures thereof. Keeping the silica and bydrogen contents low in
this preferred form, the same as aforesaid, will also provide distinctly purer cast
molten metals.
[0027] Other incidental impurities are merely those of extremely minor contaminants which
result from the ordinary impurity contents normally associated with different grades
of raw material sources for MgO, zircon, etc. The total amount of impurities should
be kept to a minimum, if possible, to reduce or avoid possible detrimental effects
to the above-noted properties and structural characteristics.
[0028] In still another feature of the present invention is directed to a method of casting
using a casting vessel comprising the steps of providing within the vessel a preheatable
molded refractory insulating liner of this invention, heating the vessel to at least
a vessel preheat temperature to initiate the development of hot strength in the preheatable
liner for casting at metal casting temperatures, and introducing a molten metal, such
as a ferrous alloy, into the vessel.
[0029] Thusly, it can be appreciated that the special features and unique advantages of
the preheatable molded refractory insulating liners of this invention makes the same
highly effective refractory liners suitable for preheating for extended periods of
[0030] By way of illustrating and providing a better appreciation of the present invention,
the following detailed description and example are given concerning the preheatable
molded refractory insulating liners resulting from the invention and their properties
or characteristics.
[0031] A preheatable molded refractory insulating liner for lining a casting vessel made
by the process of the invention is suitable for developing sufficient hot strength
at vessel preheat and metal casting temperatures which are on the order of about 1900°F.
to about 3000°F. when such a liner is heated for a sufficient period of time. For
example, a preheatable molded refractory insulating liner may comprise a liner structure
of predetermined shape, the liner structure comprising a uniform molded mixture containing
a particulate refractory component comprised of zircon and MgO refractory grain, and
a binder therefore. In addition, the preheatable liner preferably contains a fibrous
material and, if desired, minor amounts of bentonite or other suitable thioxtropic
substances.
[0032] In the specification, the term "hot strength" refers to a liner having sufficient
hot strength to support itself during extended preheating and to withstand erosion
resulting from a molten metal entering a vessel during casting. In other words, the
preheatable liners made and used in accordance with the teachings of this invention
unexpectedly and advantageously generally do not soften or weaken, collapse or wash
away after being preheated by a molten metal entering the vessel, as currently experienced
with other prior art preheatable liners. Additionally, the preheatable liners of the
present invention are less prone to contaminate the molten metals because of their
low free silica and low hydrogen contents.
[0033] In a preferred embodiment, the preheatable molded refractory insulating liners are
formed of by weight of about 75% to about 98.5% a particulate refractory component
comprised of zircon and MgO refractory grain being in a ratio from about 1:1.5 to
about 1:24, respectively, about 1.5% to about 15% binder, 0% to about 10% fibrous
material and 0% to about 5% a thixotropic substance. Preferably, the zircon is about
5% to about 15%, and most preferably about 10% by weight of the liner. The zircon,
also known as zirconium silicate (ZrSiO₄ or ZrO₂ SiO₂), and sometimes known as hyacinth,
jargon, etc., can be derived from natural or synthetic products, or any other suitable
sources not inconsistent with the teachings of this invention. It has been surprisingly
discovered that when zircon, and especially finely comminuted zircon, or zirconium
silicate, is intimately mixed with MgO refractory grain in sufficient amounts and
made into a molded refractory insulating liner for a casting vessel, the zircon and
MgO refractory grain unexpectedly react at vessel preheat temperatures which are
in the range of about 1900°F. to about 2400°F. to develop sufficient hot strength
as a result of the formation of fosterite bonding when such a liner is heated for
a sufficient period of time. To this end, it is not necessary, but highly preferable,
that the entire amount of zircon, or zirconium silicate, used be very finely comminuted.
For example, preferably about 95% of the zircon particles should pass through a 325
mesh screen, and more preferably substantially all should pass through a 400 mesh
screen. Most preferably, the zircon should have an average particle size of about
10 microns. In particular, ground zircon sand and especially zircon flour, for instance,
are suitable sources of highly comminuted zircon to be employed pursuant to the invention.
The term zircon employed herein is to be understood in each instance as referring
to a chemical combination of zirconium, silicon and oxygen designatable by the formula
ZrSiO₄ and irrespective of its origin be it synthetic or natural.
[0034] In carrying out the invention, the MgO refractory grain, also known as magnesium
oxide or magnesia, can be derived from any suitable sources and especially from sources,
such as natural, seawater or brine magnesite, periclase grain, or any other suitable
sources, or mixtures thereof. The magnesite or periclase grain, however, preferably
is of the type commonly referred to as dead burned magnesite or dead burned periclase.
By "dead burned" magnesite or periclase is meant magnesite or periclase fired to high
temperatures to produce a hydration resistant grain consisting essentially of well-sintered
low porosity periclase crystals and this grain structure distinguishes it from the
more reactive lower temperature calcined caustic magnesites. Nevertheless, it should
be understood that it is preferred that the MgO refractory grain content, whether
derived from natural, seawater or brine magnesite, periclase grain, or other suitable
sources, should be substantially pure. By "substantially pure", it means containing
at least about 80% MgO by weight on the basis of an oxide analysis, with the remainder,
if any, being only minor amounts of incidental impurities. Generally, the best results
are achieved when the particle size distribution of the MgO refractory grain is not
too coarse or too fine. Preferably, such particles should be sized so that no more
than about 40% are retained on a 50 mesh screen and no more than about 40% can pass
through a 325 mesh screen. More preferably, no more than about 15% of the MgO refractory
grain particles should be retained on a 50 mesh screen and no more than about 30%
should pass through a 325 mesh screen.
[0035] It is surprisingly found that the use of a blend of different magnesite sources for
MgO refractory grain achieve the best results. As noted above, the blend should be
of sources for MgO refractory grain having an MgO content of at least about 80%. Additionally,
sources for MgO refractory grain should be selected to minimize silica and hydrogen
content. Further, sources of MgO refractory grain should be selected on the basis
of their low tendency to hydrate due to their high dead burning temperatures and as
a result of their composition. For example, it is astonishingly found that a blend
of equal parts of about 88% MgO magnesite and about 95% MgO magnesite is optimal for
minimizing silica and hydrogen content while still achieving a strong sinter and hot
strength. The 95% MgO magnesite contains about 2% to about 3% SiO₂ and the 88% MgO
magnesite contains about 7% to about 8% SiO₂. Thus, in a most preferred form of the
present invention, the preheatable molded refractory insulating liners comprise by
weight about 10% zircon, about 40% of an about 88% MgO magnesite and about 40% of
an about 95% MgO magnesite wherein the zircon and MgO refractory grain are in a ratio
of about 1:8, respectively, about 1.5% to about 15% binder, 0% to about 10% fibrous
material, and 0% to about 5% a thixotropic substance.
[0036] A suitable refractory filler may be added in acceptable amounts to the particulate
refractory component which comprises zircon and MgO refractory grain. Exemplary of
such fillers are olivine and zirconia wherein the olivine may be by weight of the
liner from 0% up to about 70% and the zirconia may be by weight of the liner from
0% up to about 80%. When a refractory filler is added to the particulate refractory
component, however, it should be understood that such a mixture will still be by weight
of the preheatable liner from about 75% up to about 98.5% as aforementioned. It should
further be understood that the zircon and MgO refractory grain are in the stated ratios
not inconsistent with the teachings of this invention so that sufficient hot strength
is developed in the preheatable liners at vessel preheat temperatures and metal casting
temperatures. It should additionally be understood that the refractory fillers preferably
should have a particle size approximating the size distribution of the MgO refractory
grain. The advantages to adding a refractory filler to the particulate refractory
component include, for instance, a reduction in manufacturing cost or to improve the
corrosion resistance of the liner. An example of a preheatable refractory liner containing
olivine as a refractory filler has a composition comprising by weight olivine about
62%, zircon about 4%, MgO refractory grain about 25%, binder about 1.5% to about 15%,
fibrous material 0% to about 10% and a thixotropic substance 0% to about 5%. It can
be noted that in this exemplary composition the MgO refractory grain and zircon ratio
by weight is about 6:1, respectively.
[0037] The binder component may be derived from any suitable binder or mixtures of binders
of those known in the refractory making and allied industries including organic and/or
inorganic binders. Typically, vessel preheating is conducted at about 1900° F. to
about 2400° F. and more typically between about 2000°F. and 2300°F. These preheat
conditions cause the organic binders incorporated within the liners to burn out,
for instance, starting at the hot face and sometimes throughout the entire board thickness,
of course, depending upon preheat time, temperature and board thickness. Nonetheless,
up until the point of burnout, the organic binders serve to hold or bind the other
materials together and comprises by weight of the liner from about 1.0% to about 10%.
Samples of organic binders suitable to be employed in the liners include, starches,
cereals, natural or synthetic resins, such as amino resins, phenolic resins or mixtures
thereof. More particularly, the phenol-formaldehyde and urea-formaldehyde resins
are best suited for use and most preferably is the phenol-formaldehyde resin. It should
be appreciated that when the phenol-formaldehyde resin is employed, a catalyst such
as hexamethylenetetraamine, also known as HMTA, Hexa, methenamine, hexamine, aminoform,
etc., should be added in sufficient amounts to polymerize the phenolformaldehyde
resin to bond the refractory grains for making a rigid structure suitable for use
as a liner.
[0038] In addition to providing binding support prior to the burnout of organic binder,
the inorganic binder generally serves to stick or hold the particulate refractory
component together during preheat conditions particularly after the organic binder
has been consumed or burnt out. To this end, it is believed that the inorganic binder
forms a glassy or viscous phase under preheat conditions developing characteristics
suitable for sticking or binding the particulate refractory component together. In
other words, an inorganic binder can act as a temporary binder characterized as a
low melting fluxing material which aids in maintaining the particulate refractory
component together subsequent to organic burnout under preheat conditions and until
the fosterite refractory bonding develops. Examples of inorganic binders suitable
for use are boric acid, borax, colemanite, etc., and preferably boric acid. Generally,
boric acid comprises by weight from about 0.5% to about 5% of the structure. In addition,
upon heating boric acid is converted to B₂O₃ which advantageously promotes sintering
of the MgO refractory grain for improving the hot strength of the preheatable liner.
[0039] The fibrous materials may comprise inorganic fibrous materials such as rockwool,
slag wool, glass wool, refractory aluminum silicate fibers, and especially slag wool;
and organic fibrous materials such as cellulosic materials derived from paper, paper
wood, sawdust, wood meal, synthetic organic fibers or the like, and particularly paper.
These fibrous materials generally serve to reinforce the preheatable liners so that
the liners are not damaged by any impact during the manufacturing, shipment and installation.
Additionally, the fibrous materials serve to prevent the particulate refractory component
from settling out of the slurry and to control porosity and permeability of the liner.
Further, by the use of such a fibrous material, the resulting preheatable liners can
become a porous board which has low bulk density, whereby the heat-insulating effect
thereof is improved. As noted above, the fibrous materials represents by weight of
the liner from 0% to about 10% and preferably about 5%.
[0040] As to the incorporation of a thixotropic substance, it generally acts as a thickening
agent or forming aid during preparation of the desired shape and generally comprises
by weight of the liner from 0% to about 5%. Exemplary of thixotropic substances are
bentonite, methylcellulose, alginates, etc., and especially bentonite. As to the bentonite,
it is preferred that the calcium bentonite is employed as opposed to the sodium bentonite.
[0041] The preheatable molded refractory insulating liner structures resulting from the
method of the invention are suitable for the forming linings for casting vessels,
such as hot tops, ladles, tundishes, troughs and pipes etc., which are intended to
contain molten ferrous alloy metals. The versatility of these structures enables them
to be shaped, for example, into the form of a plurality of predetermined shaped inserts.
Preferably, the preheatable liners are in the form of a plurality of shaped boards
employed in tundishes.
[0042] As is conventional in the art of refractory insulating liners, manufacture can be
readily done, for instance, by vacuum forming or injection molding methods which,
for example, comprise forming an aqueous slurry of solids comprising a mixture con
taining a particulate refractory component, a binder therefore and, most preferably,
a fibrous material component. Bentonite or other suitable thixotropic substances may
also be employed as discussed above. Because of the copious amounts of water utilized
in making the aqueous slurry, vacuum sources which are well-known in this art for
removing substantial amounts of water are preferably employed. The raw batch of materials
are suitably proportioned to provide the desired final mixture and preferably are
intimately premixed in the slurry form prior to vacuum forming. After the preparation
of a sufficient amount of a desired slurry, the material is usually poured into preformed
molds of the desired shape and subjected to sufficient sub-atmospheric or vacuum
conditions to suck away a substantial amount of the liquid in the slurry so that
the formed shapes can be removed from the mold and dried. The wet vacuum formed shapes
are passed through conventional hot air dryers to remove or evaporate virtually all
the water and to heat the entire structure thickness to a suitable temperature for
curing the organic and/or inorganic binder. The thickness of the liner when making
a board may range, for instance, from about 3/4 of an inch to about 2 inches.
[0043] The method of casting of the invention using a casting vessel which serves to transfer
molten metals, such as ferrous alloys, comprises the steps of providing in the casting
vessel a preheatable molded refractory insulating liner structure of this invention,
heating the casting vessel to at least a vessel preheat temperature to initiate the
development of hot strength in the preheatable liner structure for casting at metal
casting temperatures and introducing a molten metal, such as a ferrous alloy, into
the casting vessel.
EXAMPLE
[0044] The following represents two preferred compositions A and B for manufacturing a preheatable
molded refractory insulating liner in accordance with this invention:
Composition |
Ingredient |
% |
A |
Phenol-formaldehyde resin |
2.30 |
|
Hexamethylenetetraamine |
0.20 |
|
Paper |
1.40 |
|
Slag wool |
3.30 |
|
Calcium bentonite |
1.60 |
|
Magnesite: about 88% MgO |
40.60 |
|
Magnesite: about 95% MgO |
40.60 |
|
Zircon Flour |
10.00 |
|
|
100.00% |
Boric Acid 2.5% of dry batch weight. |
Composition |
Ingredient |
% |
B |
Phenol-formaldehyde resin |
2.30 |
|
Hexamethylenetetraamine |
0.20 |
|
Paper |
1.40 |
|
Slag wool |
3.30 |
|
Calcium bentonite |
1.60 |
|
Magnesite: about 88% MgO |
24.50 |
|
Zircon Flour |
4.00 |
|
Olivine |
62.70 |
|
|
100.00% |
Boric Acid 1.0% of dry batch weight. |
TABLE I
Effect of Preheat and Contact with Molten Steel on the Porosity of the Tundish Board
Manufactured with Composition A Disclosed in the Example |
PREHEAT |
POROSITY |
SPECIFIC GRAVITY |
Prior to preheat |
50.95% |
3.33 g/cc |
After 1 hour 2100°F Preheat |
56.03% |
3.55 g/cc |
AFTER CASTING |
POROSITY |
SPECIFIC GRAVITY |
Sample - 6 inches under metal line |
|
|
1 heat - medium carbon steel, medium manganese steel |
|
|
Hot Face - (11/16" thick) |
22.2% |
3.44 g/cc |
Cold Face - (3/4" thick) |
54.3% |
3.57 g/cc |
Sample - 18 inches under metal line |
|
|
1 heat medium carbin steel, 1.50% manganese steel |
|
|
Hot Face - (5/8" thick) |
14.5% |
3.37 g/cc |
Cold Face - (3/4" thick) |
53.9% |
3.51 g/cc |
GUNNABLE TUNDISH COATING |
|
|
After 1 heat sample uniform throughout 1" thick coating |
34.6% |
3.40 g/cc |
[0045] Preheat increased the porosity by 10% by burning out organic binders sintering and
reacting to form fosterite. This effect was also observed by the increase in specific
gravity when the low specific gravity organic material was removed.
[0046] Table I shows that after contact with a molten ferrous alloy, the preheatable refractory
board formed a dense (approximately 20% porosity), impermeable 0.5 inch thick layer
in contact with the steel. The porosity of the cold side of the board remained high
at about 55%. The dense hot face contained some closed pores and some oxide contamination
which lowered the apparent specific gravity compared to the cold face and the preheated
specific gravities.
[0047] X-ray diffraction showed that zircon and MgO refractory grain was consumed, and that
fosterite and cubic zirconia were formed at tundish preheat condition and both fosterite
and cubic zirconia were found present in the hot face and the cold face of the tundish
boards after casting ferrous alloys.
[0048] In use, the dense board hot face which developed resisted and reduced erosion and
steel contamination. The high porosity on the back of the board advantageously gave
lower thermal conductivity through the board, thus, lower temperatures at the permanent
lining and less heat loss from the vessel resulted. Such boards had low erosion with
high manganese steels, low hydrogen contribution to the steel and were preheated to
about 2300°F for up to about seven hours without adversely affecting their hot strength
during casting. The gunnable coating referred to in Table I had an intermediate (34%)
porosity through its entire thickness. It failed to develop a dense layer at the hot
face.
[0049] It was observed that the preheatable tundish boards developed sufficient hot strength
and remained substantially rigid and intact during the vessel preheat temperatures
and metal casting temperatures.
1. A method of making a preheatable molded refractory insulating liner structure of
predetermined shape having insulating porosity for temporarily lining a casting vessel
and for developing sufficient hot strength to maintain the integrity of the structure
at vessel preheat and metal casting temperatures which are in the range of about 1900°F.
to about 3000°F. during its use as a liner in a casting vessel,comprising making a
molded uniform mixture having a substantial insulating porosity on the order of about
50% prior to preheating containing a particulate refractory component in an amount
of about 75% to about 98.5% by weight of said preheatable liner structure of a mixture
of zircon and MgO refractory grain wherein said zircon and MgO refractory grain are
in a ratio of about 1:1.5 to about 1:24, respectively, and adding a binder for said
component and inorganic fibrous material in sufficient amounts to maintain the predetermined
shape of insulating porosity at least prior to the preheat temperatures wherein said
zircon and MgO refractory grain are of a particle size in said preheatable liner structure
to facilitate the formation of fosterite bonding which results in increased hot strength
with substantial maintenance of insulating porosity and shape without substantial
shrinkage at both the vessel preheat temperatures of about 1900°F to about 2400°F
and higher metal casting temperatures when said preheatable liner structure is used
as a liner in a casting vessel and heated for a sufficient period of time.
2. A method of making a preheatable insulating liner as claimed in claim 1 wherein
the vessel is either a hot top, ladle, tundish, pipe or trough.
3. A method of making a preheatable insulating liner as claimed in claim 1 or 2 wherein
said liner structure is in the form of a plurality of shaped inserts.
4. A method of making a preheatable insulating liner as claimed in any of the preceding
claims wherein said MgO refractory grain comprises magnesite, periclase or mixtures
thereof.
5. A method of making a preheatable insulating liner as claimed in any of the preceding
claims wherein said binder component is an inorganic binder.
6. A method of making a preheatable insulating liner as claimed in any of the preceding
claims wherein the liner includes an organic fibrous materials.
7. A method of making a preheatable liner as claimed in any of the preceding claims
wherein said inorganic fibrous material is slag wool or alumina silicate.
8. A method of making a preheatable insulating liner as claimed in any of the preceding
claims wherein said zircon is about 5% to about 15% by weight of the liner structure.
9. A method of making a preheatable insulating liner as claimed in any of the preceding
claims wherein the liner structure comprises about 75% to about 98.5% by weight of
said particulate refractory component, 1% to about 10% of said fibrous material, about
1.5% to about 15% of said binder component and 0% to about 5% of a thixotropic substance.
10. A method of making a preheatable insulating liner as claimed in any of the preceding
claims comprising a refractory filler comprising olivine or zirconia, if olivine being
present in an amount of weight of said liner structure ranging from 0% to about 70%
and said zirconia is in an amount by weight of the liner ranging from 0% to about
80%.
11. A method of casting with a vessel which serves to transfer molten metals wherein
the vessel is temporarily lined with a preheatable molded refractory insulating liner
structure prior to preheating of predetermined shape having insulating porosity, and
method comprises the steps of providing in the vessel the preheatable molded refractory
insulating liner structure of predetermined shape which is suitable for developing
sufficient hot strength to maintain the integrity of the structure at vessel preheat
and metal casting temperatures which are in the range of about 1900°F to about 3000°F
wherein the preheatable molded refractory insulating liner structure comprises :
a) a molded uniform mixture having a substantial insulating porosity on the order
of about 50% prior to preheating containing a particulate refractory component in
an amount of about 75% to about 98.5% by weight of said preheatable liner structure
of a mixture of zircon and MgO refractory grain wherein the zircon and MgO refractory
grain are in a ratio of about 1:1.5 to about 1:24, respectively, and
b) a binder for the component and inorganic fibrous material in sufficient amounts
to maintain the predetermined shape of insulating porosity at least prior to the preheat
temperatures wherein the zircon and MgO refractory grain are of a particle size in
the preheatable liner structure to facilitate the formation of fosterite bonding which
results in increased hot strength with substantial maintenance of insulating porosity
and shape without substantial shrinkage at both the vessel preheat and higher metal
casting temperatures when the preheatable liner structure is heated for a sufficient
amount of time; heating the vessel to at least a vessel preheat temperature of about
1900°F to about 2400°F to initiate development of hot strength in the preheatable
liner structure for casting at metal casting temperatures; and introducing a molten
metal into the vessel with substantial maintenance of insulating porosity and shape
of said liner structure without substantial shrinkage.
12. A method as claimed in claim 11 wherein the vessel is a hot top, a ladle, tundish,
pipe or trough.