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Sommaire du brevet 1062916 

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(12) Brevet: (11) CA 1062916
(21) Numéro de la demande: 1062916
(54) Titre français: METHODE D'INTRODUCTION DE PRODUITS DE TRAITEMENT DE TERRE ALCALINE DANS LES COULEES D'ACIER
(54) Titre anglais: METHOD OF INTRODUCING ALKALINE-EARTH TREATING AGENTS INTO STEEL MELTS
Statut: Durée expirée - au-delà du délai suivant l'octroi
Données bibliographiques
Abrégés

Abrégé anglais


ABSTRACT OF THE DISCLOSURE
A method of introducing alkaline-earth
metal treating agents into steel melts in a deoxidized
or nondeoxidized state wherein a siliceous-oxide-free
slag is applied to the melt and the treating agent in
finely-divided form is blown into the melt in a carrier
gas. The treating agent is introduced at a depth of
greater than 2000 mm, preferably about 2700 mm.

Revendications

Note : Les revendications sont présentées dans la langue officielle dans laquelle elles ont été soumises.


The embodiments of the invention in which an exclusive
property or privilege is claimed are defined as follows:
1. A process for the treatment of a steel melt with
an alkaline-earth metal treating agent which comprises the steps
of:
(a) forming a deoxidized or nondeoxidized steel
melt in a ladle lined with a material free from siliceous oxide;
(b) covering said melt with a synthetic siliceous-
-oxide-free slag; and
(c) injecting into said melt a quantity of said
treatment agent equal to the quantity thereof which stoichio-
metriccally reacts with oxygen and sulfur therein, the injec-
tion being effected at a rate less than the maximum rate of re-
action of said melt with said agent and over a period in excess
of the time required for said quantity to react with said melt
under the thermodynamic and reaction-kinetic parameters preva-
lent therein.
2. The process defined in claim 1 wherein said agent
is injected into said melt in a neutral carrier gas at a depth
at least 2000 mm below the surface of said melt.
3. The process defined in claim 1 or claim 2 wherein
said depth is about 2700 mm below the surface of said melt.
4. The process defined in claim 1 or claim 2 wherein
said melt consists of nondeoxidized steel and is deoxidized
during the treatment with said agent, said agent being intro-
duced at least over a period corresponding to the ending of
deoxidization in said melt.

5. The process defined in claim 1 or claim 2 wherein said
melt is a deoxidized steel melt and said agent is introduced
until the degree of desulfurization of said melt has attained
60%.
6. The process defined in claim 1 or claim 2 wherein the
treatment agent is capable of both deoxidization and puriffi-
cation of said melt.
7. The process defined in claim 1 or claim 2 wherein the
treatment agent is injected over a period at least twice as
long as is necessary for said quantity to react at said maximum
rate and sufficient to effect at least 60% desulfurization of
the melt.

Description

Note : Les descriptions sont présentées dans la langue officielle dans laquelle elles ont été soumises.


D6Z9~6
~ .
Field of the In~ention
The present invention relates to the treat~
ment of steel melts and, mora particularly, to the
treatment of steel melts wi~h alXaline-earth-metal
trea~ing agents.
Back round of the Invention
,g ~
It ha~ been known heretofore in steel
mQ~allurgy to treat s~eel melts in a deoxidized
or nondeoxldized sta~ with treating agents con-
taining alkaline-earth me~als. Gcnerally the
all~line-earth metals are ~he elem~ntal or pure
m~tals or are provided in mixtures, compounds or
alloys.
The moBt com~on alkaline-ea~th metals used
for this purpose ar~ calcium and m~gnesium and typicaL
treatmen~ agents include calcium carbide, calclum-
-silicon (CaSi) or calcium ferrosilicon which consists
o 30% by weight calcium, 60~/o by w~ight silicon and
10~/o by weigh~ iron.
Other trestment agents include in addi~ion
~o the calcium or magnesium and apart from silicon,
substances such as aluminum and manganeseO
-1- ~ ".

~06Z9~6
The treatm~nt agent is generally blown lnto the
melt at a depth of 2000 mm or more to increase the degree
o effec~i~eness and the reaction of the ~rea~ing agent
with the 1.nelt~
The treatment serves to purify the melt by re-
ducing the oxygen content and the content of oxidic im-
purities, improves the elimination of sulfides which may
remain aftsr desulfurization, etc.
For the mDst part the treatment quantities are
the ~oichiometric requirement and substan~ially ~o excess
unreacted alkaline-earth-metal treat~ent agent remains in
the meltO
In the conventional systems, substantially only
deoxidized steal m~l~s are treated to obtain m~xlmum utilization .-
o~ the all~line-car~h treating agentO Howeve~, it has been
recognized that the introduction of the entire quantity of
the alkaline-earth treating agent into ~he mel~ in a single
administration results in volatillzation of this agent and
hence it has been proposed to control the ra~e of addition ~:
so that at any instant in time the quantity which is added
is equal to the quantity which reactsO The reac~ion speed
depends on the thermodynamic and reaction-kinetic paramet~rs
of the total system. With this approach one is able to
achieve excellent utllization of the alkaline-eartll treating
agen~9 effective ductility and elongation to brealc and the
like. However, it is not possible to furtller improve the

OGZ9~6
~hrinkage and viscosity characteristics~ -
Ob ects of the Inv ntion
It is the principal object of the present in-
ven~ion to provide a method of or process for treating
a steel melt with an all~line-earth treating agent which
o~
i5 applicable to deoxldized4nondeoxidized steel melts and
which improv~ the ductllity and break contraction char-
acteristics of the steel and is also capable o improving
the i80tropy 0~ the systemO
Descript~on of the Inventlon
Thi~ object and other which will become apparsnt
her~ina~ter ar~ attained, in accordance w~th th& invention, ..
by a process for introducing allcaline-earth treating agents
into a steel melt whereby the st~el melt ~in a deoxidized
or nondeoxidized state) i~ introdu¢sd into a casting ladle
with a siliceou -oxlde-~ree lining, is covered with a
synthetlc slliceous-oxide~ree slag, and is ~rea~ed with
the requisite quan~ity of alkaline-earth metal treating
agent in finely divided form by blowing the treating agent
in a neutral carrier gas (e.g. argon~ into the steel m~lto
The i~vention resides in that the necessary quanti~y
_
of allualine-earth treating ag~nt is introduced in deficit
or in reduced amount below that dictated by reaction
equilibrium and over a longer period ~han i~ otherwi~e
requiredO In oth~r words if the quantity Q of the trea~lng

~o62~6
agent is stoichiometrically required by the melt and the
quantity i9 introduced at a rate R ~ which corresponds
~o the rate at ~Jhich the treating agenS is capable of
reacting with the sy~tem under the thermodynamic and
r&action-kinetic condltions mentioned abo~e, the rate R
corresponds ~o the customary rate of addltionO The trea~-
ment tim~ t will then be determined by the ralation~hip
t-Q/Ro According to the invention, however, the ~reating
agent i8 added at a rat2 R'<R and over a period t'~t~ - :
Pre~erably ~ 5 minutes and R'~ 0.6 kg
of Ca pe~ ~on of steel. The "breal~ contraction" referred ~o
hereina~ter is the percent reduction in a linesr dimension a~
break caused by the application o tensile stressO Thus
(break contraction) : ~ar~ x 100% in percen~ where d is
the linear dim~nsion (e~g. thiclcness) prior to application :~
of tensile ~tres~ and d' is the same dimension a~ter brealc.
More specifically, th~ deficit supply of
the all;aline-ear~h treating agent or agen~s m~ans tha~ the
reaction rate is limi~ed by the rats of supply which is less
than the maximum po~sible reaction rate under the thermodynamic : :.
peram~ters and reaction kinetic parameters and therefore
substantially smaller than the rate at w~ich the treating
agsnt has been supplied heretoforeO The tarm "prolonged'~
when u~ed herein to refer to the treatment time thu~ means a
~ime substantially grea~er than the treatment ~lme used for
the same quantity per ton of similar trea~ing agents heretofore~
Preferably the rate R' of the addition of the treating agent

~ o629~6
in accordance with the present invention is less than
0~5R where R is the rate of addition corresponding to the
maximum rate of reaction as de~ined above and the period
o~ addition t according to ~he invention is at least
equal to 2t where t is the addition rate for a given
quantity Q o~ the treating agent which is necessary to .!
maintain the ra~e of addition R.
Surprisingly, by the deficit and prolonged
addition ~f the alumin-~m earth treating agent, the
ductility characteristics can be increased and it is
pos~ible to lmprove substantially th~ constriction of
the r~sulting metal body at break (break contraction)
to 5O~/O or greater. The isotropy of th~se characteris~ics
is also improvedO
It has been ~ound that the introductlon of the
alkaline-earth ~rea~ing agent shouLd take place at a
depth in excess of ~000 mm, preferably about 2700 mm, in
the steel melt uslng lan~es or the likeO An important
advantage of the invention is that it can be carried out
with nondeoxidized steel melts as well 8S with deoxidized
me~ts~
When the reaction is carried out wi~h nondeoxidized
melts, the alkaline-earth treatlng agent is introduced prior
to and up to the ~ermination o~ deoxidation in the melt~
When the treatment is carried out with deoxidized ~teel
melts, the reactlon is carried out until ~he deoxidized
but yet sul~ur-containing melt has reached a desul~urizatlon
degree of 60%~
, , .,, ,i ; ~. : ,:

~629~L6
Deoxidation and desulfuriza~ion otherwise can
be carried out by any of the conventional processes.
0~ course the trea~men~ according ~o the present in-
vention can be carried out as part o the dooxida~ion
or desulfuriza~ion process or both so that the lat~ar
treatment and the alkaline-earth treatment according to
ehe inven~ion can o~erlap. The processes may b~ con- ~ .
trolled in terms of the degree of desulfurization as .
indicat0d earlier.
~leC :
A 120 ~ons nondeoxidi~d sS~el melt has a com-
position by weigh~ of:
0.17~/~ carbon ~C~
0.01% s~licon (ST3 ~ ;
0080% mangane~e (Mn~
0~01~/o phosphorous (P) ~ :
0~017% 8ulfur (S)
0.002% aluminum (Al)
Balance iron tFe)
The melt in a dolomlte-line casting ladle is
covered with 500 kg of synthetic ~lag consisting of 80%
by weighS lime (CaO) and 20% by weight calcium fluorid~
(CaF2 ) ~
The treatlng agent was 400 kg of c~lcium-silicon
(30% by welght calcium, 60% by weight ~ilicon, 3% by
: .... ....
~6- .
'' ". " ' , ", "- ~ , ," ~ ".",.. ......

1~;)6Z9~6
weight aluminum, balance iron) and was introduced in ~.
powder ~orm using aluminum as a carrier gas and through
lances to a depth oE about 2600 mm below the sur~ac~ of
the melt over a period of over twelv~ minutesO
The composition of the melt af~er inj2ction
of the calcium silicon wa6
0.17% by weight carbon
0.21% by weight silicon
0.~8Vb by weight manganese
0.012% by weig~t phosphorous
0.006% by weight sulfur
0.010% by weight aluminum ..
balance iron
The steel mel~ was cast into ingots and rolled
into 50 mm thick sheets. The break contraction-in the
thi~kness direction of the sheets was 65 ~o 68O9%o
. . . ~
~ .
110 tons of a deoxidiæed steel melt has a com-
position of
0013% by w~ight carbon
0.41% by weigh~ silicon
1~45% by w~ight manganese
0.025% by weight phosphorous
0.017% by w2ight sulfur
0.068% by weight aluminum
balance iron.

10629~i
In a casting ladle a3 deqcribed in Example I,
the steel ~elt was covered ~ith 450 kg of a synthetic
slag consis~ing o 80% by weigh~ calcium oxide and 20%
by weight calcium fluorideO
10 kg of magnesium powder and 100 kg of
ma~ne~ium ox~de powder are blown in argon into the steel .:
melt at a depth of about 2700 mm over a period of ~en
minutes~
~ er the ~reatmen~ the composition of ~he
melt is:
.
0013% carbon
0~40% silicon
1~45% manganese ..
00024% phosphorou~
0.007% sulfur
00045% aluminum
balance iron
After the steel has been rolled as described in
Example 1, the breal~ge contra~tion was 50% or reO
-8-

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Historique d'événement

Description Date
Inactive : CIB de MCD 2006-03-11
Inactive : Périmé (brevet sous l'ancienne loi) date de péremption possible la plus tardive 1996-09-25
Accordé par délivrance 1979-09-25

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Description du
Document 
Date
(aaaa-mm-jj) 
Nombre de pages   Taille de l'image (Ko) 
Abrégé 1994-04-27 1 29
Revendications 1994-04-27 2 64
Dessins 1994-04-27 1 12
Description 1994-04-27 8 272