Sélection de la langue

Search

Sommaire du brevet 1149618 

Énoncé de désistement de responsabilité concernant l'information provenant de tiers

Une partie des informations de ce site Web a été fournie par des sources externes. Le gouvernement du Canada n'assume aucune responsabilité concernant la précision, l'actualité ou la fiabilité des informations fournies par les sources externes. Les utilisateurs qui désirent employer cette information devraient consulter directement la source des informations. Le contenu fourni par les sources externes n'est pas assujetti aux exigences sur les langues officielles, la protection des renseignements personnels et l'accessibilité.

Disponibilité de l'Abrégé et des Revendications

L'apparition de différences dans le texte et l'image des Revendications et de l'Abrégé dépend du moment auquel le document est publié. Les textes des Revendications et de l'Abrégé sont affichés :

  • lorsque la demande peut être examinée par le public;
  • lorsque le brevet est émis (délivrance).
(12) Brevet: (11) CA 1149618
(21) Numéro de la demande: 368479
(54) Titre français: METHODE DE FABRICATION D'AGENTS DE DESULFURATION POUR LE FER BRUT OU L'ACIER EN FUSION
(54) Titre anglais: PROCESS FOR THE MANUFACTURE OF DESULFURIZING AGENTS FOR CRUDE IRON OR STEEL MELTS
Statut: Périmé
Données bibliographiques
(52) Classification canadienne des brevets (CCB):
  • 53/99
(51) Classification internationale des brevets (CIB):
  • C21C 7/064 (2006.01)
(72) Inventeurs :
  • BRAUN, ALBERT (Allemagne)
  • PORTZ, WILLI (Allemagne)
  • STRAUSS, GEORG (Allemagne)
  • DELHEY, HANS-MARTIN (Allemagne)
(73) Titulaires :
  • HOECHST AKTIENGESELLSCHAFT (Allemagne)
  • KRUPP STAHL AKTIENGESELLSCHAFT (Non disponible)
(71) Demandeurs :
(74) Agent: FETHERSTONHAUGH & CO.
(74) Co-agent:
(45) Délivré: 1983-07-12
(22) Date de dépôt: 1981-01-14
Licence disponible: S.O.
(25) Langue des documents déposés: Anglais

Traité de coopération en matière de brevets (PCT): Non

(30) Données de priorité de la demande: S.O.

Abrégés

Abrégé anglais


PROCESS FOR THE MANUFACTURE OF DESULFURIZING AGENTS
FOR CRUDE IRON OR STEEL MELTS

ABSTRACT OF THE DISCLOSURE:
The present invention relates to a process for the
manufacture of desulfurizing agents containing 1 - 6 %
by weight of chemically bonded water, based on calcium
oxide-containing calcium carbide, for crude iron and
steel melts. To this end, a molten mixture of calcium
carbide and calcium oxide with a CaO content of 20 to
80 % by weight is produced, which is allowed to solidify
into a block. Next, the block which still has an average
temperature of more than 400° C, is rough-crushed to
particles with a size of less than 150 mm and calcium
oxide is added to the comminuted mixture, which still
has a temperature of at least 400° C, in accordance with
the CaO content desired in the end product. The mixture
is finally ground in the presence of air or nitrogen with
a moisture content of from 5 to 20 g/m3 (at 1.013 bar and
273.15 K) at temperatures below 100° C to particles with
a size of less than 10 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:
THE CLAIMS:

1) A process for the manufacture of desulfurizing agents
containing 1 - 6 % by weight of chemically bonded
water, based on calcium oxide-containing calcium
carbide, for crude iron and steel melts, which com-
prises: producing from lime and coke a molten mixture
of calcium carbide and calcium oxide having a CaO
content varying within the range 20 to 80 % by weight;
allowing the mixture to cool and solidify into a
block; rough-crushing the solidified block while it
still has an average temperature of more than 400° C
to particles with a size of less than 150 mm, admixing
the comminuted mixture, which still has a temperature
of at least 400 ° C, with a quantity of calcium oxide
necessary to establish in the resulting mixture a
total content of CaO corresponding to the CaO content
desired in the end product, and then grinding the
mixture with thorough agitation and in the presence
of air or nitrogen with a moisture content of 5 to
20 g/m3 (at 1.013 bar and 273.15 K) at temperatures
below 100° C to particles with a size of less than
10 mm.
2) The process as claimed in claim 1, wherein coarse
particles of CaO with a size of 8 to 60 mm are added
to the rough-crushed mixture.
3) The process as claimed in claim 1, wherein a quantity
of CaO sufficient to produce a mixture containing more

-8-


than 45 % up to 90 % by weight of CaO, is added
to the rough-crushed mixture.
4) The process as claimed in claim 1, wherein the
mixture is crushed at temperatures of between
400° C and the solidification temperature.
5) The process as claimed in claim 1, wherein the molten
starting mixture of calcium carbide and calcium oxide
with a CaO content of 20 to 45 % by weight is produced
from lime and coke in customary manner by thermal treat-
ment.
6) The process as claimed in claim 1, wherein the molten
starting mixture of calcium carbide and calcium oxide
with a CaO content of more than 45% up to 80 % by
weight is produced by introducing finely divided
calcium oxide into an existing calcium carbide melt
containing up to 45 % by weight of CaO until establish-
ment therein of a maximum CaO content of up to 80 %
by weight and then allowing the whole to solidify
into a block.
7) The process as claimed in claim 1, wherein the mixture
is ground at 10 - 50° C to particles with a size of
less than 10 mm.
8) The process as claimed in claim 1, wherein the
mixture is ground to particles with a size of
less than 100 /µm.

-9-

Description

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


~96~8

HOE 79/H 051

The present invention relates to a process for the
manufacture of desulfurizing agents containing 1 - 6 %
by weight of chemically bonded water, based on calcium
oxide-containing calcium carbide, for crude iron and
steel melts.
The desulfurization of crude iron and steel melts
by means of calcium carbide (referred to hereinafter as
carbide) containing calcium oxide (briefly referred to
hereinafter as lime) is generally known (DE-PS 1 160 457,
DE-PS 20 37 758).
Heretofore, it has been customary to prepare these
desulfurizing agents by processes, wherein the required
amount of finely divided lime was introduced into molten
carbide in order to produce a homogeneous mixture in the
melt, which was then allowed to cool and was comminuted.
Preferably, the finely divided lime was introduced
into the stream of carbide tapped of~ from the furnace.
Although the amount of lime that can be introduced into
the carbide melt is limited and there are risks associated
with working with liquid carbide, it has long been hel~
in the art that this method could not be avoided since
it was thoughtthat only a mixture of CaC2 and CaO pro-
duced in the melt was ideally suited for desulfurizationof metal melts.
Desulfurizing agents based on calcium carbide that
contain substances which split off water at the temperature


'~



of the metal melt have already been described in DE-AS
22 52 795. These agents, which are mixtures of customary
commercial carbide with, for example, Ca(OH)2 as the
substance that splits off water, have the disadvantage
that they are mixtures produced by mechanical mixing
processes in which carbide particles exist separately from
the Ca(OH)2 particles, so that the use of theæ products
leads to higher consumption, irregular and vigorous gas
reactions and a large variation as regards the desulfuriz-
ing efficiency, rendering difficult any controlled use ofthese agents.
The present invention now unexpectedly provides a
process for making a highly effective desulfurizing agent
for crude iron and steel melts which process permits the
disadvantages of prior art methods to be avoided and which
comprises: thermally producing from lime and coke a molten
starting mi2ture of carbide and calcium oxide with a CaO
content varying within the range 20 to 80 %; allowing
the mixture to cool and solidify into a block; rough-
crushing the solidified block while it still has anaverage temperature of more than 400 C, preferably of
between 400 C and the solidification temperature of the
melt, to particles with a size of less than 150 mm and
calciu~ oxide; and admixing the comminuted mixture, which
still has a temperature of at least 400 C, with a
quantity of calcium oxide, necessary to establish in the
mixture a total content of CaO corresponding to the CaO
content desired in the end product. Preferably, calcium

~961~3

oxide is added in a quantity necessary to establish
in the mixture a total content of CaO of more than 45 O~G
up to 90 % by weight. Next, the mixture is gro~nd with
intensive mixing and in the presence of air or nitrogen
having a moisture content of 5 to 20 g/m3 (at 1.013 bar
and 273.15 K) at temperatures below 100 C, preferably
at 10 - 50 C, to particles with a size of less than
10 mm, preferably of less than 100 /um.
A preferred feature of the present process provides
for the molten starting mixture of calcium carbide and
calcium oxide to contain 20 to 45 % by weight of CaO,
the mixture having been obtained ~rom lime and coke in
known manner by thermal treatment. It is also possible,
however, initially to produce a molten starting mixture
of calcium carbide and calcium oxide with a CaO content
of more than 45 % up to 80 % by weight, by introducing
finely divided calcium oxide into an existing calcium
carbide melt containing up to 45 % by weight of CaO
until establishment of a maximum CaO content of up to
80 % by weight, then allowing the whole to solidify into
a block, and rough-crushing the latter at temperatures of
above 400 C.
The present process permits inhibiting mixing the lime with
a carbide melt and the di~ficulties associated therewith.
In addition to this, the present process has, inter alia,
the following beneficial effects: It is not necessary for
the composition of the burden to be set in each particular
case ~or producing the carbide melt, nor is it necessary

6~

for the lime to be first ground to a certain particle
size. Use can rather be made of a carbide block with
a CaC2 : CaO weight ratio which may vary within wide
limits, In other words, the carbide block may contain
CaC2 and CaO in practically any ratio, and the lime can
even be used in the form of coarse particles with a size
within the range 8 to 60 mm, for example.
A further beneficial effect of the agent produced
in accordance with this invention resides in the fact that
on the surface each individual particle of Ca(OH)2 lies
close to CaC2, with the result that the desulfurizing
reaction is started very early and regularly. As a re-
sult of this, smaller amounts of desulfurizing agents
are required to be used for producing comparable de-
sulfurization results, which incidentally are controllable.
The following Examples illustrate the invention:
EXAMPLE 1
The starting material was a melt as customarily usedfor the manufacture of commercial carbide, the melt con-
taining 80 % by weight of CaC2 and 20 % by weight of CaO.A carbide block of corresponding composition was produced
in known manner in a crucible by allowing this melt to
cool.
After the block had cooled to an average temperature
of approximately 600 C, it was rough-crushed to particles
with a size of less than 150 mm and the carbide, still
with a temperature of 500 C, was covered with a layer
of sufficient lime with a particle size of 8 to 60 mm

~96~8

that the resulting mixture had a total CaO content of
50 ~ by weight.
Next, the mixture was ground in a rotary mill, while
1500 m3/h of air with a moisture content of 10 g/m3 (at
15 C) was passed therethrough. The throughput was 50Q kg/h
at 50 C, and the mixture was ground to particles with a
size of up to 100 /um.
1500 kg of this product was used for customary desul-
furization of 300 000 kg of a crude iron melt th~ contained
0.03 % by weight of sulfur. The iron so treated contained
0.005 % by weight.
EXAMPLE 2
Calcium carbide was thermally produced in known
manner from lime and coke, the lime/coke mi,~ture in the
total burden being set at a weight ratio of approximately
110 : 40, corresponding to a carbide with a CaO content of
approximately 45 % by weight.
CaO of a particle size of 3 - 8 mm was metered into
the carbide tapped off, the CaO being used in a quantity
necessary to establish an average content of approximately
80 % by wei~ht of CaO in the discharge crucible (approxi-
mately 1.2 - 1.3 t of CaO per metric ton material tapped
off).
After cooling the crucible to an average temperature
of no less than 600 C, which was the case after 4 hours,
the block was rough-crushed to particles with a size of
less than 150 mm and a layer of sufficient lime of

~ 61 8

particles with a size of 8 to 60 mm was added to the
hot mixture that the average CaO content was 90 % by
weight. Next, the mixture was ground in a rotary mill,
while 1500 m3/h of air with a moisture content of
10 g/m3 (at 15 C) w~s passed therethrough. The through-
put was 500 kg/h at 50 C and the material was ground
to particles with a size of less than 100 /um.
The mixture permitted the same desulfurization
results to be produced, based on the calcium carbide
content, as described in Example 1.

Dessin représentatif

Désolé, le dessin représentatatif concernant le document de brevet no 1149618 est introuvable.

États administratifs

Pour une meilleure compréhension de l'état de la demande ou brevet qui figure sur cette page, la rubrique Mise en garde , et les descriptions de Brevet , États administratifs , Taxes périodiques et Historique des paiements devraient être consultées.

États administratifs

Titre Date
Date de délivrance prévu 1983-07-12
(22) Dépôt 1981-01-14
(45) Délivré 1983-07-12
Expiré 2000-07-12

Historique d'abandonnement

Il n'y a pas d'historique d'abandonnement

Historique des paiements

Type de taxes Anniversaire Échéance Montant payé Date payée
Le dépôt d'une demande de brevet 0,00 $ 1981-01-14
Titulaires au dossier

Les titulaires actuels et antérieures au dossier sont affichés en ordre alphabétique.

Titulaires actuels au dossier
HOECHST AKTIENGESELLSCHAFT
KRUPP STAHL AKTIENGESELLSCHAFT
Titulaires antérieures au dossier
S.O.
Les propriétaires antérieurs qui ne figurent pas dans la liste des « Propriétaires au dossier » apparaîtront dans d'autres documents au dossier.
Documents

Pour visionner les fichiers sélectionnés, entrer le code reCAPTCHA :



Pour visualiser une image, cliquer sur un lien dans la colonne description du document. Pour télécharger l'image (les images), cliquer l'une ou plusieurs cases à cocher dans la première colonne et ensuite cliquer sur le bouton "Télécharger sélection en format PDF (archive Zip)" ou le bouton "Télécharger sélection (en un fichier PDF fusionné)".

Liste des documents de brevet publiés et non publiés sur la BDBC .

Si vous avez des difficultés à accéder au contenu, veuillez communiquer avec le Centre de services à la clientèle au 1-866-997-1936, ou envoyer un courriel au Centre de service à la clientèle de l'OPIC.


Description du
Document 
Date
(yyyy-mm-dd) 
Nombre de pages   Taille de l'image (Ko) 
Dessins 1994-01-25 1 6
Revendications 1994-01-25 2 70
Abrégé 1994-01-25 1 29
Page couverture 1994-01-25 1 17
Description 1994-01-25 6 208