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Патент USA US2405861

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Patented Aug. 13, 1946
Charles William Tod, Kingswinford, Brierley
H_ill,_ England, asslgnor to Albright & Wilson
Limited, Oldbury, near Birmingham, England,
a British company
7 No _Drawing. Application September 11, 1942, Se
rial No. 458,064. In-Great Britain September
19, 1941
10 Claims. (Cl. 252—~316)
This invention comprises improvements in or
relating to the production of alginate solutions.
Alginates are capable of forming very viscous
solutions or jellies which on account of their
physical properties are valuable in various con
nections, and it is an object of the invention to
are e?ective for the purpose. These salts may be
described as molecularly dehydrated alkali metal
D01yDh0sphates. They have the property of form
ing stable complex ions with alkaline earth ions.
Surprisingly, in view of the fact that it has
only a feeble power of sequestering calcium ions,
facilitate the production of aqueous solutions, in
sodium citrate has also been found valuable in
cluding under the term “solutions” jellies, disper
this connection.
sions and emulsions containing alginates.
It is possible, within the scope of the inven
It is well known that alkaline-earth alginates 10 tion, to use an alkali alginate such as sodium
are insoluble in water. By the term "alkaline
alginate along with the calcium alginate to help
earth alginates” in this connection is meant the
to take the calcium alginate into solution. While
alginates of the metals properly and strictly called
in this case the use of sodium alginate is not
altogether avoided, the quantity employed is re
alkaline earth metals, viz., calcium, barium, and
strontium. Magnesium and beryllium do not fall 15 duced as compared with the use of sodium al
into this category (although sometimes loosely
ginate as the sole source of alginate in prepar
ing alginate solutions.
called alkaline earth metals). They di?er in
The following examples show by way of il
many ways from the true alkaline earth metals
and magnesium alginate is not insoluble in water.
lustration speci?c methods of carrying the inven
As a result of the insolubility of alkaline earth 20 tion into effect:
alginates, although alginic material is usually
Example I
separated from seaweed in the form of the cal
cium salt, it has hitherto been necessary to con
An example of the method of using the inven
tion is the preparation of a glycerin hand jelly.
vert it into the sodium salt or other soluble al
ginate in order to utilise the properties of the
This can be made by dissolving sodium citrate
alginates in forming viscous solutions and gels.
in water, adding glycerin and a preservative, and
then stirring in the calcium alginate, which is
If it were possible to bring the calcium salt di
preferably ?nely ground. With the correct con
rectly into solution instead of ?rst converting it
centrations a jelly will form in a few hours. 20
into the sodium salt this would obviate the steps
30 grams of sodium citrate‘ dissolved in 1 litre of
connected with the conversion of the material.
water witli800 c. c. glycerin is sul?cient to deal
It has, of course, been known for some time
with 30 grams of calcium alginate.
that certain sodium salts, such as the carbonate
and the sesqui-carbonate, will react with calcium
Example II
alginate to give viscous solutions, but-these are
The following is an example of the preparation
opaque because of the presence of an insoluble
of an emulsion:
salt, such as calcium carbonate.
It has now been found it is possible to produce
Sodium citrate is dissolved in water to which
has been added a preservative. Calcium alginate
directly from alkaline-earth alginates, clear vis
is stirred in until completely dissolved, and the
cous solutions or gels, by the use of certain com
pounds capable of sequestering alkaline-earth 40 desired quantity of oil is then added. After fur
ther stirring, the resulting mixture is passed
ions. such salts are known in themselves; for
through a homogeniser when it will be found to
example it is known that sodium hexametaphos
give a. stable emulsion.
phate can sequester calcium ions and, for exam
Thus 7.5 gms. of ?nely powdered calcium al
ple, prevent calcium carbonate or the like from
being precipitated out of solution in water by the 45 ginate are dissolved in a solution of 7.5 gmS. so
dium citrate in 250 cos. of water. 5 gms. of soya
use of soap. (See Schwartz and Gilmore, “In
bean oil are stirred into the resulting viscous
dustrial 8: Engineering Chemistry” vol. 26, page
solution and the product is subsequently passed
through a homogeniser.
According to the present invention a process
of preparing the solution of an alkaline-earth 50
Example III
alginate is characterised by introducing into the
so vent salts capable of sequestering alkaline
ea th ions, so as to assist solution.
It has been found that sodium hexametaphos
phate and sodium tripolyphosphate (NasPaOio) 55
The following is an example where sodium al
ginate and- calcium alginate are employed to
10 gms. sodium alginate are dissolved in 1 litre
of water and 15 grams calcium alginate are added
with stirring. A jelly is formed in a short time.
These preparations can be used as the basis
of cosmetic or pharmaceutical Jellies and, when
the nature of the compound used for reacting
with the calcium alginate permits, food Jellies
and emulsions can also be made.
I claim:
5. A process as claimed in claim 1, wherein the
salt is sodium citrate,
6. A process as claimed in claim 2, wherein
the salt employed is sodium citrate in a prbpor
;tion of about two-thirds that of the alginate.
7. A process for the preparation of a glycerine
hand Jelly which c 'mprises dissolving sodium
.citrate in water, add‘ \ glycerine and a preserva
1. A process 01' preparing a solution of an al
itive, then stirring in ?nely ground calcium al
' kaline earth alginate comprising the steps of 10 \gin'ate, and then allowing the mass to stand until
introducing into an aqueous solvent sequestering
va Jelly is formed.
salts chosen from the group consisting of molecu
3 8. A process for preparing a Jelly which com
larly dehydrated alkali metal polyphosphates and
prises dissolving about 20 grams oi.’ sodium citrate
alkali citrates and thereafter introducing alka
in about 1 litre of water, adding about 800 c. c.
line-earth alginate and forming stable complex 15 of glycerine, then stirring in about 30 grams of
ions therefrom by the action of the sequestering
calcium alginate, and allowing the mass to stand
salts thereon.
2. A process of preparing a jelly containing an
alkaline-earth alginate wherein an aqueous solu
tion is made containing a salt capable of seques 20
tering alkaline earth ions and selected from the
group consisting of molecularly dehydrated al
luntil a jelly is formed.
9. A process for the preparation of an emulsion
which comprises the steps of dissolving sodium
citrate in water to which has been added a pre
servative, stirring in a quantity of calcium algi
nate until it is completely dissolved, then adding
the desired quantity of oil, stirring the mixture,
kali metal polyphosph'ates and alkali citrates,
thereafter the alkaline-earth alglnate is dispersed
and passing it through a homogeniser.
in the solution in quantity su?icient to form a
10. The method of preparing an emulsion which
jelly, and the solution thus produced is allowed
comprises dissolving about ‘7.5 grams of ?nely
to stand until gelled.
powdered calcium alginate in a solution of about
3. Preparations containing alkaline-earth al
7.5 grams of sodium citrate in about 250 c. c. of
ginate, as produced by a process as claimed in
water, stirring in about 5 grams of soya bean
claim 2.
30 oil and passing the product through a homogen
4. A process as claimed in claim 1, wherein the
salt employed is sodium hexametaphosphate.
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