Sélection de la langue

Search

Sommaire du brevet 1106761 

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 1106761
(21) Numéro de la demande: 1106761
(54) Titre français: PROCEDE D'OBTENTION DE GELS D'HYDROXYDE D'ALUMINIUM ET PRODUITS QUI EN DERIVENT
(54) Titre anglais: PROCESS FOR PRODUCING ALUMINUM HYDROXIDE GELS AND RESULTING PRODUCT
Statut: Durée expirée - après l'octroi
Données bibliographiques
Abrégés

Abrégé anglais


A B S T R A C T
A process for producing aluminum hydroxide gels
substantially free of sodium ions involves a heterogeneous
reaction between an aqueous solution of a water soluble alumi-
num salt and an aqueous slurry of a water soluble alkaline
earth carbonate.

Revendications

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


The embodiments of the invention in which an exclu-
sive property or privilege is claimed are defined as follows:
1. A process for producing an aluminum hydroxide
gel which comprises combining water, a water soluble salt of
aluminum and a water insoluble alkaline earth carbonate under
heterogeneous reaction conditions while maintaining a reaction
pH between 4.7 and 5.5, and isolating the aluminum hydroxide
gel.
2. The process of Claim 1 in which an aqueous
solution of the aluminum salt is added to an aqueous slurry of
the carbonate.
3. The process of Claim 1 in which an aqueous
solution of the aluminum salt is gradually added to a pre-
measured volume of an aqueous slurry of the carbonate.
4. The process of Claim 1 in which a constantly
flowing stream of an aqueous solution of the aluminum salt is
continuously added to a constantly flowing aqueous slurry of
the carbonate.
5. The process of Claim 1 in which the aluminum
salt is selected from the group consisting of its chloride,
sulfate and nitrate.
6. The process of Claim 1 in which the carbonate is
selected from the group consisting of calcium and magnesium
carbonates.
7. The process of Claim 2 in which said aqueous
solution has a 14 - 28% by weight aluminum salt content.

8. The process of Claim 2 in which said aqueous
slurry has a 4 - 10% by weight carbonate content.
9. The process of Claim 1, wherein the isolated
aluminum hydroxide gel is mixed with pharmaceutically accepta-
ble excipients to provide a pharmaceutical composition in
oral dosage form.
10. A process for producing aluminum hydroxide gels
which comprises adding a 14 - 28% by weight aqueous solution
of an aluminum salt selected from its chloride, aluminum
sulfate and aluminum nitrate to a 4 - 10% by weight aqueous
slurry of a carbonate selected from the group consisting of
calcium and magnesium carbonate under agitated, heterogeneous
reaction conditions while maintaining a reaction pH between
4.7 and 5.5 by adjustment of the relative amounts of the
reactants, and isolating the aluminum hydroxide gel.

Description

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


76~
This invention relates to a process for producing
aluminum hydroxide gels of pharmaceutical grade and particu-
larly a gel product which is free of or substantially free of
sodium salts.
Physicians are becoming increasingly aware of the
fact that sodium salts are counterindicated for persons having
hypertension and other cardio-vascular diseases and for persons
having renal impairment. For instance, such persons are
instructed to eliminate or severely curtail their consumption
of table salt. If such persons have gastrointestinal disorders
~hich are medicinally benefited by antacids, including aluminum
hydroxide gel, it is quite important that the gel not be con-
taminated by entrained sodium ions. A process which produces
aluminum hydroxide gel with no appreciable sodium ion content,
at a relatively low cost, is desirable.
Prior processes for producing aluminum hydroxide gel
have not been entirely satisfactory either because the process
produced a gel product which included an undesirably large
amount of sodium salts or because the process was too complex
and expensive to be commercially practicable. According to one
prior process, aluminum chloride is reacted with sodium carbon-
ate but this has required extensive flushing with wash water to
remove the sodium chloride. Another known process involves
reacting sodium aluminate with gaseous carbon dioxide but this
also involves using considerable wash water to reduce the
sodium ion content to an acceptable level.
The patent 3,066,012 to C.P. Wilson, Jr. et al is of
interest because it involves as a first step the reaction of an
aluminum sulfate solution with calcium carbonate to form a
basic aluminum sulfate sol, the second step of isolating the
sol, the third step of adding a sodium carbonate solution to

1~6763L
form the alumina gel and the fourth step of washing out the
sodium salts and other soluble impurities. This process
involves a series of homogeneous step-wise reactions. The com-
mercial processes mentioned earlier above likewise involve
homogeneous reactions.
The process of the present invention involves a
heterogeneous reaction in water between a water soluble alumi-
num salt such as aluminum chloride and an alkaline earth carbon-
ate such as calcium carbonate. These reactants should be
selected or be properly purified to minimize sodium, iron and
other contaminants. The process can be carried out either as a
batch or as a continuous operation. A definite advantage of
the chemical reaction is that it may occur at ambient atmos-
pheric pressure and temperature. In either a batch or a con-
tinuous process reaction should be allowed to continue for at
least from 5 to 20 minutes.
Aluminum chloride is the preferred aluminum salt
reactant and it should constitute from 14 to 28% by weight of
the solution which is used. Calcium carbonate is the preferred
carbonate reactant and it should constitute from 4 to 10% by
weight of the aqueous slurry which is used. These two aqueous
preparations are combined in a relative amount so that the
reaction bath is maintained between about pH 4.7 and 5.5. This
will generally require the addition to 100 grams of calcium
carbonate of from 70 to 90 grams of aluminum chloride but it is
preferred that the reaction conditions be controlled on the
basis of the pH of the reaction.
The exact nature of the heterogeneous reaction is not
fully understood but it would appear that the fixing of the
carbonate by the solid calcium carbonate insures that carbonate
is present at the site of precipitation. This gives the alumi-

76~
num ion the immediate opportunjty of complexing with the carbon-
ate, which results in the most reactive and stable gel. This
stabilizing reaction is evidenced by a split of the carbonate
band in the 1400 - 1500 cm 1 region of the infrared spectrum.
The precipitated aluminum hydroxide gel is isolated
from the reaction bath and then washed to obtain it in a puri-
fied form. A unique feature of this process is that the gel
product which it produces is considerably more reactive than
gels produced by present day commercial processes. Because of
its exceptional acid consuming capacity it is particularly
valuable as a medicinal antacid.
Instead of aluminum chloride, other water soluble
aluminum salts may be substituted, such as for example the
sulfate or the nitrate, an amount being used to yield the same
aluminum content. Instead of calcium carbonate, other water
insoluble alkaline earth carbonates may be substituted, such as
for example magnesium carbonate, an amount being used to yield
the same carbonate ion content.
In a batch operation it is preferable, but not
essential, to add the aluminum salt in its water solution, to a
reactor vessel containing the alkaline earth carbonate in its
aqueous slurry. The vessel should be equipped with a stirrer
or other mechanical agitator and the aluminum salt solution
should gradually be added to it. Representative examples are
the following:
EXAMPLE 1
A total of 5000 ml. of water was charged to an agi-
tated reactor under ambient conditions and 210 gm. of U.S.P.
calcium carbonate was added and dispersed, thus forming a
slurry. Aluminum chloride solution (28% by weight) was then
fed to the slurry at a rate of 15 ml./min. until a total of

676~
490 ml. solution had been fed. The reaction bath assayed gener-
ally a pH 5.0 - 5.5 at the end of this addition. The resulting
aluminum hydroxide gel was isolated as by filtration and given
several water washes.
The 4% aluminum hydroxide gel suspension ~hich was
prepared from the gel slurry exhibited the following properties:
Assay, % Al 23 8.53
pH 6.70
Viscosity, cps 1 488
Acid consumption, ml.
O.l N HCl/gm. 25.2
CaO, % O. 44
Chlorides, % Q.04
EXAMPLE 2
In Example 1, magnesium carbonate was substituted for
the calcium carbonate and the product assayed as follows:
Assay, % A~ 23 6.98
pH 7.10
Viscosity, cps 1 084
Acid consumption, ml.
O.l N HCl/gm. 25.2
Mg(OH)2, % 0.38
C 1 , % _ _ _ _
EXAMPLE 3
In Example 1, aluminum sulfate was substituted For
the aluminum chloride.
EXAMPLE 4
This illustrates a continuous process in which the
reactants are constantly being added and intermixed with each
30 other and the resulting product is isolated.
A calcium carbonate slurry, maintained at a con-
sistency to contain 5% CaC03 by weight, and an aluminum

chloride solution, maintained at a consistency to contain 14%
by weight AlC13, were fed simultaneously to an agitated reactor
at ambient pressure and temperature. The calcium carbonate
feed rate was about 1 gal/min and the aluminum chloride feed
was maintained by a pH controller-reactor system to give a
reactor pH around 5Ø Overflow from the reactor, containing
the aluminum hydroxide gel slurry, was filtered and washed on a
rotary filter.
The 4% aluminum hydroxide gel suspension prepared
from this partlcular reaction showed the following properties:
Assay, % A1203 8.09
pH 6.50
Viscosity, cps 420
Acid consumption, ml.
0.1 N HCl/gm. 26.2
CaO, % 0.86
Chlorides, % 0.15
EXAMPLE 5
In Example 4, magnesium carbonate was substituted for
the calcium carbonate and the product assayed as follows:
Assay, % A1203
pH 7.10
Viscosity, cps 1358
Acid consumption, ml.
0.1 N HCl/gm. 24.7
Mg(OH)2, % 0.44
C 1 , %
EXAMPLE 6
In any of the above examples the relative amounts of
the reactants can be varied within the limits of this in-
vention.
The foregoing examples are to be construed as illus-

trations of this invention and are not considered to be limi-
tations thereof.
EXAMPLE 7
The aluminum hydroxide gel obtained in any of
Examples 1-4 is mixed with pharmaceutically acceptable excipi-
ents to form a pharmaceutical composition in oral dosage form.
~'
.. , .' ~ , . .
.., ,..., - : ,,
. , . . . . ~ .

Dessin représentatif

Désolé, le dessin représentatif concernant le document de brevet no 1106761 est introuvable.

États administratifs

2024-08-01 : Dans le cadre de la transition vers les Brevets de nouvelle génération (BNG), la base de données sur les brevets canadiens (BDBC) contient désormais un Historique d'événement plus détaillé, qui reproduit le Journal des événements de notre nouvelle solution interne.

Veuillez noter que les événements débutant par « Inactive : » se réfèrent à des événements qui ne sont plus utilisés dans notre nouvelle solution interne.

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 , Historique d'événement , Taxes périodiques et Historique des paiements devraient être consultées.

Historique d'événement

Description Date
Inactive : Périmé (brevet sous l'ancienne loi) date de péremption possible la plus tardive 1998-08-11
Accordé par délivrance 1981-08-11

Historique d'abandonnement

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

Titulaires au dossier

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

Titulaires actuels au dossier
S.O.
Titulaires antérieures au dossier
GREEN B. GLASSCOCK
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
(aaaa-mm-jj) 
Nombre de pages   Taille de l'image (Ko) 
Abrégé 1994-03-17 1 11
Revendications 1994-03-17 2 44
Dessins 1994-03-17 1 10
Description 1994-03-17 6 153