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| United States Patent | 4139546 |
| Link to this page | http://www.wikipatents.com/4139546.html |
| Inventor(s) | Berger; Paul D. (Missouri City, TX);
Benavides; Tomas J. (Missouri City, TX) |
| Abstract | An anionic silicone defoamer having the following general formula:
##STR1##
wherein: R is alkyl;
X is 1 to 20;
Y is 1 to 10;
Z is 2 to 4, and;
M is a monovalent cation.
The anionic silicone defoamer is made, for instance, by reacting
dimethyldichlorosilane, trimethylchlorosilane, and beta-cyanoethyl
methyldichlorosilane in the presence of aqueous sodium hydroxide. Dry
detergent compositions containing the present anionic silicone composition
exhibit reduced foaming, even after several months of storage. |
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Title Information  |
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Drawing from US Patent 4139546 |
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Anionic silicone defoamer |
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| Publication Date |
February 13, 1979 |
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| Filing Date |
September 6, 1977 |
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Title Information  |
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Description  |
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This invention relates to anti-foaming agents and more particularly to
novel anionic silicone defoamers useful in agricultural and detergent
compositions. Specifically, the present invention relates to the
incorporation of certain siloxanes as foam inhibitors in detergent
formulations to reduce the foaming tendency of such formulations in water.
The present compositions are also useful in liquid hydrocarbons,
particularly low vapor pressure fuels used as power fuels which have a
tendency to foam when agitated in the presence of air or gases.
Heretofore, various conventional anti-foam agents, such as polyglycols and
morpholine as well as other organopolysiloxanes have been used in
hydrocarbons with varying degrees of success.
In Bluestein et al., U.S. Pat. No. 2,992,083, granted on July 11, 1961, it
is proposed to provide certain cyanoalkyl polysiloxanes as effective foam
inhibitors particularly for low vapor pressure hydrocarbon fuels.
Bluestein et al. utilized only cyano polymeric compositions with no
reference or suggestion to the use of the present alkali polysiloxanes in
detergent formulations or in hydrocarbon power fuels.
In Farminer et al., U.S. Pat. No. 3,843,558, granted on Oct. 22, 1974, it
is proposed to coat sodium tripolyphosphate with an organopolysiloxane.
There is no suggestion of an alkaline form of any polysiloxane as an
anionic defoamer.
Nitzche et al., in U.S. Pat. No. 3,235,509, granted Feb. 15, 1966, propose
trimethylsiloxy end-blocked polysiloxanes as effective anti-foaming agents
in aqueous alkaline systems.
In U.S. Pat. No. 3,650,401, granted on Feb. 2, 1971 to O'Hara et al.,
anti-foaming agents are disclosed which are effective in aqueous media.
These agents are formed from a polysiloxane, an inorganic oxide, and a
basic material.
While the prior art anti-foam agents are to some degree effective, a
satisfactory defoamer which is stable and effective in the presence of
large amounts of nonionic and/or anionic surfactants, such as found in
detergent laundry solutions, was not available before this invention was
made.
It is therefore an object of this invention to provide an improved anionic
silicone defoamer and a novel method for making same.
It is another object of this invention to provide an anionic silicone
defoamer as aforesaid wherein the defoamer is prepared and used in the
alkaline form of the silicone.
It is another object of this invention to provide an anionic silicone
defoamer as aforesaid in an effective one-step reaction.
It is still another object of this invention to provide an anionic silicone
defoamer as aforesaid wherein the defoamer retains its stability in the
presence of large amounts of nonionic and/or anionic surfactants.
It is still another object of this invention to provide an anionic silicone
defoamer as aforesaid which is useful in detergent formulations.
Broadly stated the defoamer of the present invention may be represented by
the following Formula I:
##STR2##
wherein: R is alkyl, preferably methyl and/or ethyl;
X is 1 to 20;
Y is 1 to 10;
Z is 2 to 4; and
M is a monovalent cation such as ammonium or an alkali metal, the latter
being preferred.
The method of preparing the defoamer of the present invention may be
broadly stated as reacting a dialkyldihalosilane, trialkylhalosilane, and
a beta-cyanoalkyl alkyldihalosilane in the presence of a hydroxide; such
as sodium, potassium, lithium, or ammonium hydroxide.
Chlorosilanes are generally preferred, dimethyldichlorosilane and
trimethylchlorosilane are commercially available, and are particularly
preferred. The beta-cyanoalkyl alkyldichlorosilane may be prepared as
disclosed in U.S. Pat. No. 2,922,083, granted July 11, 1961; U.S. Pat. No.
2,860,153, granted Nov. 11, 1958; and U.S. Pat. No. 2,837,551, granted
June 3, 1958.
The preferred preparation of reaction ingredients to make the product of
the present invention is as follows:
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Approximate Approximate
Reactant Weight Range Moles
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Dimethyldichlorosilane
65-130 gm 0.5-1.0
Trimethylchlorosilane
22 gm 0.2
Beta-cyanoethylmethyl-
dichlorosilane 19-60 gm 0.1-0.3
Sodium Hydroxide
(40% Wt. Aqueous)
150-310 gm 1.5-3.0
Solution) (of solution)
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In a preferred embodiment in Formula I, X is 5 to 10, Y is 1 to 3, and Z is
2 or 3.
The anionic defoamer of the present invention may be employed in commercial
preparations where foaming is a problem, such as in herbicides, detergents
and cleansers, adhesives, cutting oils and lubricants, textile dyes, latex
paints, and fuel oils.
Suitable detergents useful pursuant to the present invention include the
sulfonates and phosphates, and particularly the linear alkyl benzene
sulfonates. A concentration of anionic silicone defoamer of up to about 1%
by weight of the detergent composition is generally sufficient to produce
the desired effect.
Generally, it is desirable to use the present anionic silicone defoamers in
concentrations of about 0.1 to 0.5 percent by weight. The specific
proportion to be used being determined by the artisan in each particular
instance. The anionic silicone defoamers of the present invention remain
stable in dry detergent compositions even after several months of storage.
EXAMPLE I
First, 129 grams (i.e. 1 mole) of dimethyldichlorosilane are mixed with
38.6 grams (i.e. 0.2 moles) of betacyanoethylmethyldichlorosilane.
Then, 290 grams of a 40% aqueous solution of sodium hydroxide is added
dropwise over a 30 minute period at room temperature to the above mixture,
followed by 21.6 grams of trimethylchlorosilane.
The entire mixture is stirred and allowed to react for one hour and the
product is allowed to separate from the salt water phase formed during the
reaction.
A yield of 88% of a colorless oily liquid product is obtained.
EXAMPLE II
This example demonstrates the use of the present invention as a defoamer in
detergent compositions.
Forty grams of the product obtained from Example I is absorbed on 25 grams
of powdered silica. Then 0.162 grams of this absorbed product is added to
100 grams of a commercial heavy duty laundry detergent. A 5 percent
solution of this detergent mixture in water at 120.degree. F gives no foam
when agitated in a Hobart mixer for thirty minutes. This detergent
solution without the anti-foamer from Example I, foams over in less than 5
minutes.
The foregoing dry detergent formulation containing the anti-foamer of the
Example I remains stable and effective after shelf storage for over three
months.
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Description  |
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