Patent US2749316 - Stabilised sodium aluminate - Google Patentsuche 2017-01-26, 4*11 PM

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Stabilised sodium aluminate Verffentlichungsnummer US2749316 A

US 2749316 A Publikationstyp Erteilung
Verffentlichungsdatum 5. Juni 1956
Eingetragen 5. Mai 1952
ZUSAMMENFASSUNG auf verfgbar Priorittsdatum 17. Aug. 1951
Erfinder Bernard Coates Kenneth
Ursprnglich
Ici Ltd
Bevollmchtigter
BILDER (2) Zitat exportieren BiBTeX, EndNote, RefMan
Patentzitate (3), Referenziert von (6), Klassifizierungen (17)

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BESCHREIBUNG (OCR-Text kann Fehler enthalten) ANSPRCHE auf verfgbar

STABILISED SODIUM ALUIVIINATE Kenneth Bernard Coates, South Kensington,
London,

England, assignor to Imperial Chemical Industries Limited, a corporation of Great Britain No Drawing. Application May 5,
1952, Serial No. 286,207

Claims priority, application Great Britain August 17, 1951 4 Claims. (Cl. 252-182) This invention relates to compositions which
consist preponderantly of sodium aluminate and which, on dissolution in water, yield clear, substantially colorless solutions
which are stable on standing for prolonged periods.

The particular object of the invention is to provide a dry powdered form of sodium aluminate intimately mixed with up to 2 /2 of
a stabilising agent, so that on dissolving the product in water the traces of iron which get into the sodium aluminate during its
manufacture are restrained from coloring the solution or being precipitated as discrete brown-colored particles. Sodium
aluminate is used in the manufacture of paper and in the preparation of lake colors; and for such uses, in which the aluminium
hydroxide is ultimately precipitated, colored or patchy precipitates would be objectionable. Even 0.01% Fe2Oz which
precipitates is sometimes objectionable but the critical amount depends on the chemical or physical condition of the iron.

Dry sodium aluminate which contains molecular proportions of Na20 to A1203 of at least 1.3 :1 is relatively stable and gives
solutions in water which do not precipitate appreciable amounts of aluminium hydroxide. However, with less than 1.3 moles of
Na20 per mole of A1203 in the sodium aluminate, the latter is somewhat unstable in water and aluminium hydroxide is
precipitated. In order to get a low ratio aluminate, i. e. one containing less than 1.3 moles of Na20 per mole of A1203, which
yields stable solutions of restricted alkalinity, it has previously been proposed to make a sodium aluminate product by drying
solutions thereof to which a stabilising agent, such as Rochelle salt, a tartrate, saccharate, gluconate, pyrogallate, sugar,
dextrin, starch, glycerol, glycol or phenolate, has been added, the heating of the solution during drying being limited to 200 C.,
so that a relatively hydrated product containing 20% water is obtained.

In contrast to these prior proposals, the present invention is concerned primarily, though not exclusively, with sodium
aluminate compositions containing Na20 and A120 in molecular ratio of at least 1.3:1, which have been dried by heating until
virtually anhydrous, so that the water content is reduced to 5% or less and in which there is present an unavoidable trace of
iron which has occurred due to the presence of soluble iron compounds at some stage of manufacture or has been picked up

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during drying or other processing in iron vessels. Such compositions may contain as little as 0.01% Fe203 but in fact
anhydrous sodium aluminate generally contains from 0.03 to 0.1% Fe203.

When such substantially anhydrous and highly alkaline sodium aluminate, containing traces of iron oxide as impurity, is
dissolved in water, the solution obtained is neither clear nor colorless. It becomes necessary to find some means of dissolving
this iron in the aqueous sodium aluminate solution without interfering with the precipitation of aluminium hydroxide when the
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solution is used in papermaking or similar applications involving its precipitation. Moreover, the iron must remain dissolved
patents.
during this precipitation of aluminium hydroxide, which is normally Patented June 5, 1956 effected by dilution or by addition of
such reagents as will lower the pH of the solution. Furthermore, if an additive is used for keeping the iron dissolved it must be
virtually inert to all other processes involved and must only be used commercially in relatively small amounts.

It has been found that substances which are normally used in large excess to prevent precipitation of iron and aluminium
during chemical analysis, and those proposed for stabilising the more or less hydrated form of low alkalinity sodium aluminate
described above, such as tartaric acid or Rochelle salt, are insufhciently eifective in industrially practicable amounts to give
clear colorless stable solutions of the substantially anhydrous aluminate containing iron as impurity, suitable for use in paper
or color lake industries. However, we have discovered that mannitol and/ or sorbitol, and apparently only these two
compounds, stabilise solutions of anhydrous sodium aluminate containing traces of iron sufficiently to give clear, colorless
solutions which remain clear and colorless even after standing for many days. Moreover, when aluminium hydroxide is
precipitated from these stabilised solutions during the processes of papermaking or lake manufacture, the precipitate is
uniformly white.

Mannitol and sorbitol are asymmetric hexahydric al cohols and both have been found to have essentially the same effect in
solubilising the iron impurity in alkaline sodium aluminate. The proportion of stabilising agent employed might be varied,
dependent upon the quantity of iron oxide present as impurity. Generally speaking, the stabilising agent should be used in a
quantity suflicient to prevent precipitation of the iron oxide when the aluminate is dissolved in water. Under preferred
conditions, from A to 2 /2% by weight of the sodium aluminate should be stabilising agent.

According to a specific embodiment of our invention, therefore, we provide a dry composition comprising an intimate mixture
of powdered, virtually anhydrous sodium aluminate containing about 1.3 moles of Na20 per mole of A1203, traces of iron
oxide, and from A to 2V2% by weight of a stabiliser selected from the group consisting of mannitol and sorbitol. With 0.01%
F6203 present in the sodium aluminate, of mannitol or sorbitol is suflicient to produce the desired effect; with 0.1% Fe203
present, 22 /2 of mannitol or sorbitol is required. The resulting mixtures are stable on keeping for long periods and dissolve in
water to produce clear, colorless, stable solutions.

In its broadest aspects, our invention comprises stabilised sodium aluminate containing from 1.2 to 1.4 moles of NazO per
mole of A1203, a trace of iron oxide as impurity, and a stabiliser selected from mannitol and sorbitol in sufficient amount to
prevent the trace of iron oxide present from precipitating upon dissolution of the aluminate in water.

For application where the stabilised sodium aluminate is to be dissolved in hard waters containing calcium and/ or
magnesium, we prefer also to incorporate therein a sequestering agent to prevent precipitation of the calcium or magnesium.
Any of the conventional sequestering agents may be used although the preferred agent is the disodium salt of
ethylenediamine tetra acetic acid. The amount of sequestering agent added depends upon the hardness of the water, but 5%
by weight of the preferred agent in the stabilised aluminate will produce a clear solution in a water of 200 p. p. m. hardness in
terms of CaCOs.

In a further feature, therefore, our invention also comprises sodium aluminate which forms clear, colorless solutions on
dissolving in water, containing 50-54% by weight of A1203, 39-42% by weight of Na20, %2 /2% by weight of a stabiliser
selected from the group consisting of mannitol and sorbitol, and V2-3% by weight of disodium ethylenediamine tetra acetate,
the remainder being water and traces of iron oxide.

All the above compositions may be made by milling the aluminate and additives together in standard mixing equipment in the
appropriate proportions. As the proportions of additive are small, we prefer to mix together a small proportion of the aluminate
with all the additive, and, to usethis as a master batch to mix with the remainder of the aluminate and thus make it easier to
prepare an intimate mixture. For reasons of adequate mixing, we prefer to use mannitol because it is a solid not only at
ordinary temperatures but also at somewhat elevated temperatures. Ribbon mixers, pug mills and similar equipment may be
used, and the mixing should becontinued energetically for at least minutes, preferably for from 1 0 to minutes to insure
thorough mixing of the aluminate and additives.

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The invention is illustrated bu not. restricted by. the following example showing the use of mannitol as a stabilising agent for
anhydrous sodium aluminate.

Example- T o 100 parts by weight of anhydrous sodium aluminate powder, containing about 1.3 moles of NagO per mole of
A1203, and 0.05 F2Q3 as impurity, was added 1 part by weight of mannitol in the form of adry powder, and the whole mass
was then thoroughly mixed in a ribbon mixer for 15 minutes. A uniform free-flowing powder was obtained which remained
unchanged and free-flowing on storage in a sealed bottle. 2 /2 parts by weight of the composition were dissolved in 100 parts
by weight of soft water and gave a clear colorless solution which remained clear and colorless after standing for 11 days in a
stoppered' bottle.

Substantially equivalent results were obtained using sorbitol in lieu of the mannitol utilised in the preceding example or
mixtures of sorbitol and mannitol.

The novel principles of this invention are broader than the specific embodiments recited above and, rather than unduly extend
this disclosure by attempting to list all the numerous modifications which have been conceived and reduced to practice during
the course of this development, these novel features are defined in the following claims.

I claim:

1. As a new composition of matter, substantially anhydrous sodium aluminate containing about 1.3 moles of NazO per mole of
A1203, a trace of iron oxide as impurity and from A to 2 /2% by weight, based on the iron-oxide containing aluminate, of a
stabiliser which prevents precipitation of the iron oxide impurity on dissolution of said composition in water, said stabiliser
being selected from the group consisting of mannitol and sorbitol.

2. The composition of claim 1 including the sequestering agent disodium ethylenediamiue tetra acetate.

3. A composition of matter consisting essentially of a dry mixture of powdered substantially anhydrous sodium aluminate
containing from 1.2 to 1.4 moles of NazO per mole of A1203 and from 0.01 to 0.1% by weight of iron oxide as impurity, and
from /4 to 2 /2% byweight of the iron oxide-containing aluminate of a stabiliser which prevents precipitation of said iron oxide
impurity on dissolution of said composition in Water, said stabiliser being selected from the group consisting of mannitol and
sorbitol.

4. As. a new composition of matter, substantially anhydrous sodium aluminate in a form which provides a clear, colorless
solution in water, said sodium aluminate comprising from to. 54% by weight of A1203, 39 to 42% by Weight of NazO, to 2 /2%
by weight of a stabiliser selected. from the group consisting of mannitol and sorbitol and /2 to 3% by weight of disodium
ethylenediamine tetra acetate, the remainder being water and traces of iron oxide.

References Cited in the file of this patent UNITED STATES PATENTS.

1,157,436. Spence et al. Oct. 19, 1915 2,345,134 Lindsay et al. Mar. 28, 1944 2,544,649 Bersworth Mar. 13, 1951 OTHER
REFERENCES Thorpes Dictionary of Applied Chemistry, vol. 7, 4th ed. 1946, page 504; vol. 2', 4th ed. 1938, pages 282,
296. Longmans, Green and C0,, N. Y. C.

Paper Trade 1;, v. No. 8, pp. 131-3 (1940).

PATENTZITATE
Zitiertes Patent Eingetragen Verffentlichungsdatum Antragsteller Titel
Company Of Peter
US1157436 * 18. Aug. 1914 19. Okt. 1915 Solution of sodium aluminate.
Spence & Sons Ltd
Sodium aluminate product and process of producing the
US2345134 * 27. Nov. 1939 28. Mrz 1944 Nat Aluminate Corp
same
Caustic alkali composition of matter and its use as a
US2544649 * 14. Jan. 1949 13. Mrz 1951 Bersworth Frederick C
polyvalent metal precipitationinhibitor
* Vom Prfer zitiert

REFERENZIERT VON
Zitiert von Patent Eingetragen Verffentlichungsdatum Antragsteller Titel
Stockholms Superfosfat Fab Process of wet-spinning fibers containing
US2967085 * 29. Mai 1957 3. Jan. 1961
Ab polyacrylonitrile
Stockholm Superfosfat Process of wet-spinning fibers containing
US2967086 * 29. Mai 1957 3. Jan. 1961

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Stockholm Superfosfat Process of wet-spinning fibers containing

US2967086 * 29. Mai 1957 3. Jan. 1961
Fabriks polyacrylonitrile
US4007252 * 2. Sept. 1975 8. Febr. 1977 Borg-Warner Corporation Stabilized sodium aluminate solutions
US4252735 * 13. Okt. 1978 24. Febr. 1981 Handy Chemicals Limited Stable aqueous alkali metal aluminate solutions
US4629603 * 3. Dez. 1984 16. Dez. 1986 W. R. Grace & Co. Method of inhibiting cold end corrosion in boilers
EP0112525A1 * 7. Dez. 1983 4. Juli 1984 Giulini Chemie GmbH Agent and process for neutral sizing
* Vom Prfer zitiert

KLASSIFIZIERUNGEN

US-Klassifikation 106/499, 423/265, 106/505

Internationale Klassifikation C09B63/00, C01F7/02, C01F7/04, C01F7/00, D21H17/66, D21H17/00
Unternehmensklassifikation C01F7/04, C09B63/00, D21H17/66, C01F7/02
Europische Klassifikation C01F7/02, C09B63/00, D21H17/66, C01F7/04

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