CA1225903A - Hydrocarbon oil based silicone antifoams - Google Patents

Abstract

HYDROCARBON OIL BASED SILICONE ANTIFOAMS
ABSTRACT

Hydrocarbon oil based antifoams compositions containing a hydrogen-silicon copolymer, a hydrophobic filler, an organo-silicone surfactant, a hydrocarbon carrier oil and optionally a silicone oil act to effectively defoam concentrated solutions, including those containing ionic surfactants or protein based solutions. The use of the hydrocarbon oil based silicone antifoams represents an inexpensive route to defoams difficult solutions.

Description

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HYDROCARBON OIL BASED SILICONE ANTIFOAMS
.
BACKGROUND
The present invention relates to a novel hydrocarbon oil based antifoam composition.
Antifoams based on hydrocarbon oils, such as mineral oil, that contain dispersed hydrophobic solid particles are well known ln the art. Although effective in easy-to-defoam solutions of high surface tension, their performance is much more variable in concentrated surfactant solutions particularly those containing ionic surfactants.
This limitation arises, in part, from the intrinsically higher surface tension of hydrocarbon oils relative to other antifoam vehicles such as silicone oil. To overcome this problem, various compounds have been suggested to increase the rate or extent of spreading of the antifoam. These agents are generally low to intermediate hydrophilic-lyophilic balance (HLB) nonionlc surfactants tnat are soluble or dispersible in hydrocarbon oil, such as disclosed in U.S. Patent 3,076,768. However, their effect is often variable and their utility has been questioned, (see, for example, U.S. Patent 3,207,698 and GB Patent 1,166,877).
Because hydrocarbon oil, and particularly mineral oil, is a relatively inexpensive antifoam vehicle, it is desirable to develop a hydrocarbon oil based antifoam that is highly effective in difficult-to-defoam aqueous based surfactant or protein solutions.
It has now been found that certain clearly defined mixtures of specific hydrocarbonsilicone ~2S~

.

copolymers, organo-silicone surfactants and fillers such as silica are highly effective with hydrocarbon oil as an~ifoams for these difficult-to-defoam surfactant solutions. Furtnermore, certain combinations have high antifoam performance in ionic foaming solutions while other are particularly suited to defoaming nonionic surfactant or protein based solutions.
The use of hydrophobic silica in hydrocarbon oil based antifoams is well known as dlsclosed in U.S. Patents 3,076,768; 3,207,698;
3,388,073 and 3,714,068. U.S. Patents 3,912,652 and 3,959,176 deal with the use of hyarophobic silica in polyoxyethylene and polyoxypropylene copolymers.
The use of hydrophllic sllica that lS
activated, in situ, in a non-silicone oil based antifoam is disclosed in U.S. Patent 3,304,266 for a water insoluble polyalkylene oxide and in G.B.
1,166,877 using an alkoxy silicone chloride as the hydrophobing agent.
The use of intrinslcally hydrophobic fillers in organic liquids is well known. For exampLe, Canadian Patent 508,856 discloses N,N
distearyl ethylene diamine in white spirits, while the use of finely divided polyolefin polymers or polyesters dispersed in organic liquids in discloseo in U.S. Patent 3,705,859. A conventional organic surfactant is alleged to improve the performance of the latter compositlon. The use of fatty acid salts is disclosed in G.B. Patent 1,267,482 while low molecular weight polyethylenes (500-25,000) in combination with mineral oil and conventiona-l organic nonionic emulsifiers is disclosed in U.S.
Patent 3,909,445.

9~)3 The use of surfactants to promote spread1ng and to improve the performance of hydrocarbon oil-silica antifoams is claimed in UOS. Patents 3,076,768 and 3,408,306, but these surfactants are conventional organic surfactants or emulsifiers.
The efficacy of such spreading agents is questioned in U.S. Patents 3,207,698; and 3,714,068 and G.B.
Patent 1,166,877.
U.S. Patent 3,691,091 describes the use of organo-silicone compounds to improve the performance of silicone oil-silica based antifoams. However, the organo-silicones are of a different type than that used in the present invention.
The use of silicone-glycol copolymers in association with silicone oil and sllica is disclosea in various Dow Corning Patents: U:S.
Patents 3,746,653; 3,784,479 and 3,865,544. The concentrations claimed are 70-9~.9 wt. %. The compositions of the present invention employ a hydrocarbon oil, such as mineral oil, as the vehicle ana not a silicone oil.
None of the patents cited above mentions the use of hy~rocarbon-silicone copolymers of the type disclosed herein, in combination with a hydrocarbon carrier oil and a hydrophobic filler.
Nor do these patents describe the use of organo-silicone surfactants of the type found effective here, in hydroca~bon oil oased antifoams.
SUMMARY OF THE INVENTION
The present invention provides a novel hydrocarbon oil based sllicone antifoam composition which comprises (a) from 1 to 60 weight percent of a hydrocarbon-silicone copolymer; (b) from 1 to 20 ~L~r~ 33 weight percent of a hydrophobic filler having a particle size on the average o~ from 200 to 5,000 A;
(c) from 0 to 25 weight percent of an organo-silicone surfactant of the general formula R" R R R"
R' - Si - O - (O- Si)L- (OS~ OSi - R' (1) R R' (CH2)x R

wherein R, R', and R" are individually alkyl gr`oups having from 1 to 18 carbon atoms, inclusive, P i5 either a polyoxyethylene group, a polyoxypropylene group or a mixture tnereof which can be terminated with either an alkyl or hydroxyl group and L and ~
are such tnat the surfactant is liquid, has limited solubility, and an HLB value of from 4 to 14; (d) from 20 to 97 weight percent of a hydrocarbon carrier oil; and (e) optionally from 0 to 20 weight percent of a silicone oil.
The present invention also provides a process for defoaming certain solutions employing the novel hydrocarbon oil based silicone antifoam composition. Of particular interest is the capacity for defoaming solutions containing ionic surfactants or proteln based solutions.
DETAILED DESCRIPTION OF THE INVENTION
In accordance with the present invention there is provided a novel hydrocarbon oil based antifoam composition which comprises (a) a hydrocarbon-silicone copolymer; (b) ~inely divided hydrophobic filler particles; (c) an organo-silicone surfactant; (d) a hydrocarbon carrier oil; and (e) optionally a silicone oil.

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As is well known in the art, effective liquid antifoams are those that can spread on the surface of a foaming solution. The criteria for spreading is:
> O
F A AE (2) where ~F is the surface tension of the foaming solution, ~A is the surface tension of the antifoam and ~AF is the interfacial tension between the antifoam and the foaming solution. The role of the hydrocarbon-silicone copolymer is to reduce the surface tension of the hydrocarbon oil and thus by equation (1) increase its spreading ability. It has been found that hydrocarbon-silicone copolymers meeting the following requirements are particularly effective. First, they shoula dissolve in the hydrocarbon carrier oil so as to avoid segregation in this phase. Second, they should be sufficiently surface active at the oil/air interface to decrease the surface tension at a reasonably low concentration.
Ingredients that have been found particularly well suited to this application are hyorocarbon-silicone copolymers. Many useful hydrocarbon-silicone copolymers are known in the art which could be employed in the present invention.
Although not intended to be strictly limited to any partlcular hydrocarbon-silicone copolymer, three generic classes of such copolymers are deemed particularly useful in this invention.
One class of copolymers that has been found to be particularly effective in the present i!9C)3 appllcation is the copolymer represented by the formula:
R' R''' (CH3)3-Si-O[Si-O]x- [Si-O]y - Si(CH3)3 R~ ~ 2)n-1 (3) R

Wherein R is an alkyl, aryl, aralkyl or alkaryl group containing from six to thirty carbon atoms inclusive, preferably from six to eighteen;
R', R" and R''' are individually selected from the group consisting of methyl, ethyl, propyl, hydrogen, hydroxy, and phenyl groups provided that no more than 5% of the total of R', R~ and R''' groups are hydrogen,hydroxy, phenyl or a combin~tion thereof, and the proportions of dialkylsiloxane (x) and alkylmethylsiloxane (y) groups in the polymer as well as the alkyl chain length are selected so as to meet the solubility-spreading criteria in a given hydrocarbon carrier oil. The value of n can vary so long as the ~ CH2 content is as specified. With mineral oil, which is a highly preferred hydrocarbon carrier oil, it has been found that the specific values of x, y, n in equation (3) can be varied over very board limits provided that the % CH2 content is in the range of about 30% to about 70%, preferably between 45% and 65%. When R is phenyl or alkaryl n can equal one. The % CH2 content can be calculated in any of a number of ways but for illustration only, when R, R', R'' and R'" are methyl the % CH2 = (n-l)y _ X 100 (4) (n-l)y + 2(x+y) +6 2S~3 The art of making these compounds is well known and described as, for example, by W. Noll in "The Chemistry and Technology of Silicones", Academic Press, N.Y., 1968. Either random or block copolymers of this type can be utilized.
Other copolymers that have utility in the present antifoam are the non-hydrolyzable ABA block copolymers of the structure:
R' C~H3 R3 - (CH2)n-1 [Si ~ ]x~ Si-(CH2) n-l R (5) Rn c~3 and the hydrolyzable ABA block copolymers of the structure:
R' R - 0 - [SiO]x (6) ~ Another class of copolymers that have demonstrated utility are the non-hydrolyzable ABZ
block copolymers of the structure:
R' R' R' (7) (CH3)3 Si-O ~(SiO)x (Sio-(CH2)n_lSiO)y]z~Si~(CH3)3 ~n Rn Rn and the hydrolyzable ABZ block copolymers of the structure:
R' (CH~)3-SiO-[(Sio)x (CH2)y]z~ OSi-(CH3)3 (8) R"
wherein R,RI,Rn,x,y and n have the same significance as set forth above and z is an interger all chosen so as to meet the solubility and spreading criteria already set forth and a ~ CH2 content within the required range.

~2~ 3 The proportion of copolymer used in the present antifoam composition can be between 1 to 60 percent by weight and preferably is between 5% and 20%.
The second component of the instant antifoam composition is a hydrophobic filler that is well dispersed in the hydrocarbon carrier oil.
The hydrophobic filler can be of any type of mineral that is conventionally employed in making antifoams, such as powdered alumina, titania, silica, pearlite or clay minerals, preferably silica, and more preferably a fumed or precipated silica of an average particle size of 200 to 5,000 A, that has been hydrophobized by pretreatment or by an insitu heating..
The surface of the inorganic solid can be rendered hydrophobic by various treatments before it is incorporated in the antifoam. Such treatments involve reacting the mineral with organic, silicone, or organo-silicone reagents having at least one of the following functional groups: -OH, -NH2, -SH, -NHR, -NR2, -NR3 or-NR4, which can interact with the organic filler surface. The -OH group can include the -Si-OH groups most often formed by hydrolysis of chlorosilanes. Typically used reagents include disilazanes or silanes having alkyl groups containing one to eight carbon atoms, such as hexamethyldisilazane, octadecyltrichlorosilane or trimethyl chlorosilane; primary, secondary, tertiary, or quaternary alkyl or alkylether amines having eight to eighteen carbon atoms in the alkyl group.
A typical process for making hydrophobic filler particles consists of tumbling the fine .

.. 9.

silica with the appropriate hydrophobizing agent and suitable amounts of a solvent. The product is then heated in an oven at a moderate temperature for two hours.
It has been found that the hydrophobization can also be accomplished by an in situ procedure similar to that used in making silicone oil antifoams. Here, a hydrophilic silica such as a fumed silica is incorporated and well dispersed, via high shear, into a solution of the hydrocarbon-silicone copolymer dissolved in a hydrocarbon carrier oil The mixture is then heated under moderate shear for about 2 hours to activate the surface. It has been found that the reaction temperature required for activation can be greatly reduced by incorporation in the reaction mixture of small quantities (0.1 to 1%) of a basic catalyst to facilitate the reaction of silica with a polydimethylsiloxane. Many examples of such basic catalysts are disclosed in U.S. Patent 3,560,401, and include, by way of example, the alkali and alkaline earth hydroxides. The preferred basic catalysts are the alkali metal silanolates.
Another class of potentially suitable fillers for the present application is made up of naturally or intrinsically hydrophobic solids that are known to be effective antifoam fillers.
Examples of such materials are polyolefin polymers (U.S. Patent 3,705,8S9); thermoplastic polyesters (U.S. 3,705,859); polyvalent metal salts of alkyl carboxylic acids (G.B. 1,267,482); amides of long chain fatty acids and mono and polyamines (Canadian Patents 922,456;926,261;943,035); long chain fatty alcohols (G.B. 1,386,042) and low molecular weight polyethylenes (U.S. 3,909,~45).

)3 The hydrophobic filler particles can be present in the antifoam composition at a total level of between l and 20 weight percent preferably between 2.5 and 7%. The filler can be a single species or can be a mixture of several different types.
The organo-silicone surfactant has several functions in the antifoam composition. First, it improves the spreading power of the antifoam over the bubble surface and in this way effectively distributes the antifoam. A second important function of the silicone surfactant is to reduce the adsorption of an ionic surfactant on the surface of the antifoam droplet and thus minimize the electrical repulsive forces that inhibit the transport of antifoam to the bubble surface. An additional function of the organo-silicone surfactant found in the present study is to facilitate the emulsification of the antifoam compositions.
Preferred organo-silicone surfactants are those having the following structure.

Rn R R Rn R' - Si - (O - Si)L - (OSi)M - OSi - R' (9) R R' (, 2)x P

where R, R' and R" are individually alkyl groups having from one to eighteen carbon atoms or hydrogen, hydroxy or phenyl groups provided that total of such R,R' and R" does not exceed 5%~ -Preferably they are methyl groups. P is a polyalkoxy group having from 2 to 4 carbon atoms, ~22~;9C~3 such as polyoxyethylene, polyoxypropylene, or a mixture thereof, and can be terminated by either an alkyl or hydroxyl group. L and M are chosen so that the resulting surfactant is liquid, has limited solubility in both the aqueous ~oaming solution and antifoam oil phase and has an HLB in the range of 4-14, preferably 8-11. And x has a value of from two to fiveO
Typical examples of such sur~actants are:
(Me3) SiO - (SiMe2O)20 - (MeSIiO)3.2 3 (10) C3H6(Oc2H4)7ocH3 (Me3) SiO - (SiMe2O)7 - (MeSiO)3 - SiMe3 (11) C3H6(Oc3H6)l2.5 4 9 (Me3) SiO - (SiMe2O)37 - (MeSiO)3 (12) C3H6(Oc2H4)7ocH3 Techniques for making such organo-silicone surfactants are disclosed in numerous patents and publications such as, for example, in U.S. Patents

2,834,748; 2,917,480; 3,398,104; 3,402,192;

3,507,815 and 3,741,917..
The proportions of silicone surfactant in the antifoam composition ranges between 0 an.d 25 weight percent, preferably between 0.5 and 10% and most preferably between 0.5 and 3%. It has been found that the organo~silicone surfactant is a very important ingredient when the antifoam composition is designed for foaming solutions containing ionic 2~3 surfactants. However, in certain less demanding antifoam applications the silicone surfactant may not be required. This is why the 0% level has been included in the preferred range.
Another component of the instant antifoam composition is an hydrocarbon carrier oil that makes up the balance of the composition, except for when a silicone oil is also employed. Generally, this proportion ranges from between 20 to 98 weight percent.
Any of a broad number of water immiscible hydrocarbon oils can function as the carrier oil.
These include, but are not limited to, the ~ollowing types of oils: normal liquid hydrocarbons such as tetradecane or hexadecane; branched paraffins such as isooctane; complex saturated hydrocarbon liquids composed of paraffinic and naphthenic molecules commonly known as mineral oils or liquid paraffins;
complex products of the distillation of petroleum having boiling points greater than 140C such as kerosene, heating oils or mineral spirits;
triglyceride oils such as trioleins; vegetable oils such as palm oil or olive oil and the like; and alkyl benzenes or other alkyl aryl compounds.
It has been found, however, that mineral oils are particularly well suited to serve as hydrocarbon carrier oils because of their relative inertness and compatibility within the range of components described above. Furthermore, it has been found that mineral oils having viscosities between 15 and 70 cST, preferably 25 to 60 cST, (at the temperatures for which they are used as antifoams) produce highly effective antifoams and are thus preferred carrier oils. It should be noted )3 that in some instances the hydrocarbon oil can be partially (up to 25~) replaced by an oil soluble viscosity additive t such as polyisobutylene.
The antifoam composition may optionally contain from about 0 to 20 weight percent oE a silicone oil. The use of any silicone oil known in the antifoam art is considered within the scope of the invention. Such oils include the polyorganosiloxane with a viscosity in the range of about 5 to 100,000 centistokes meaured at 25C as taught in US Patent 4,076,648.
The antifoam compositions consisting of the components described above can be prepared in any manner suitable and are generally prepared by the following sequence:
(a) The hydrocarbon-silicone copolymer (i) and hydrocarbon carrier oil are combined and ~ixed in the proportions described above.
(b) The hydrophobic filler is thereafter blended into the above mixture (a) and is then dispersed. This dispersion step depends on the type of filler used. For example, if the filler is a pre-hydrophobized material such as silica, low shear mixing is sufficient for incorporation. However, if in-situ hydrophobization is emplo~ed, a higher shear and heat treatment is required (activation). For this case, incorporation of a catalyst is desirable as discussed above~ In other cases that employ intrinsically hydrophobic fillers a crystallization step may be desirable to achieve the optimal particle size.
(c) The organo-silicone surfactant if desired, is then blended into the above mixture (b).
The antifoam composition prepared in steps (a) to (c) can be used neat, i.e., as 100~ active.

~Z~3 Alternatively, it can be emulsified in water by any of the well know emulsification techniques.
Suitable emulsifiers for this purpose are:
polyoxyethylene alcohols; sorbitan or glycerol fatty acid esters; polyoxyethylene fatty acid esters; and mixtures of the same. Additionally, the antifoam composition of the present invention may be blended with other known antifoam composition already commercially available.
The final emulsion contains 1-~0% of the active antifoam compound and can also contain suitable stabilizers as are often used with such emulsions.
The antifoams so prepared, following the teachings disclosed herein, have been found to be highly effective and superior to several commercial antifoams.
Whereas the exact scope of the instant invention is set forth in the appended claims, the following specific examples illustrate certain aspects of the present invention and, more particularly, point out methods of evaluating the same. However, the examples are set forth for illustration only and are not to be construed as limitations on the present invention except as set forth in the appended claims. All parts and percentages are by weight unless otherwise specified.
ANTIFOAM PERFORMANCE
Antifoam performance was tested by a nitrogen bubbling technique. In this procedure, nitrogen is sparged via glass frit through a surfactant solution contained in a 1 liter graduated cylinder. The volume of foam generated is found to S9~)3 be a reasonably linear function of sparging time, i.e., Vf = Rt (13) where Vf is the foam volume, t i~ the time and K
is a constant dependant on the flow rate and foaming solution.
The antifoam efficiency is defined as the rate of incr~èase in foam volume of a given surfactant solution relative to a solution that contains a given concentration of antifoam.
Thus, antifoam efficiency = Ko/K, where K
and Ko are the foaming rates in the presence and absence of antifoam, respectively. An antifoam efficiency equal to 10 indicates that a ten-~old increase in the time required to generate a given volume of foam has been produced by the presence of the antifoam. An antifoam efficiency equal to 1 indicates ~he absence of any antifoam activity. For this technique to be meaningful, the rate of bubble production must be well controlled. Not only must the gas flow rate be controlled but also attention must be paid to the cleanliness of the glassware particularly the glass frit. It is important to clean the frit thoroughly before each run~ For this purpose an alcoholic ROH solution followed by chromic acid and finally rinsing well with distilled water is satisfactory.
COMPONENTS
Surfactant solutions that were used in the present evaluations are listed in Table 1. They represent models of high foaming anionic (SDS), nonionic (15-S-9) and protein based (FF) foamants.
These solutions were freshly prepared before each determination of antifoam performance.

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Table 1 Test Solution Active Foamant Supplier 0.5~ SDS Sodium dodecyl ~. M. Laboratories, sulfate (98 + ~ Inc.
purity) O.5% 15-S-9 TERGITOLT~5-S-9, Union Carbide Corp.
secondary alcohol ethoxylate 103 FF Protein based fire National Foam Systems, fighting foam Inc.

Table 2 illustrates the convention that will be used to identify either random or block hydrocarbon silicone copolymers throughout the following examples.
Table 2 Copolymers Abbreviation Identity Type Random hydrocarbon- MDXDlyM(R) M = (CH3)3-Si-O
silicone copolymer D = (CH3)2Si-O
D' - (CH3)Si-O

ABA Block Copolymers RDnXR Dn - (CH3)2-si-O

.EXAMPLES
. Table 3 illustrates the reduction in surface tension that is achieved by dissolving a typical hydrocarbon-silicone copolymer in mineral oil. The mineral oil of this example is sold by Atlantic Ridgefield under the tradename ArcoprimeTM
200. A marked reduction in surface ten~ion is evident at a fairly low copolymer concentration.

.

. . .

Table 3 Wt.%
~ydrocarbon~SiliconeSurface Tension, Co~olymer(a)~dyne cm~l) 0 31.0 1.0 25.8 5.0 25.7 10.0 24.8 20.0 24.0 100.0 22.4 (a)MDlooD'17.5M (C18H37) Example 1 This example illustrates the importance of the key ingredients described in the previous section. Antifoams AF1-AF6 whose compositions are set forth in Table 4 were prepared in the following manner. The desired parts of mineral oil (Arcoprime 200) and hydrocarbon silicone copolymer were combined and mixed for 10 minutes at speed #2 using a ~obart laboratory mixer (Model N-50). Hydrophobic silica (Tullenox 500 from Tulco Corporation) was added and the mixture stirred for 15 minutes (speed #2).
Finally, the desired amount of an organosilicone surfactant was added and the dispersion was blended for 10 minutes at Speed #2. The resulting antifoam was an opaque uniform viscous liquid.
The performance of antifoams AFl-AF6 was tested by the Antifoam Performance methods set forth above using a 0.5~ sodium dodecyl sulfate (SDS) solution which is a well known example of an anionic surfactant that has a high foaming capacity and which is difficult to defoam. The results of these tests are recorded in Table 5. It is seen that only those antifoams containing the key ingredients described in the previous section, i.e., hydrocarbon-silicone ~LZ;2 S9~

copolymer, hydrophobic filler, organo-silicone surfactant and hydrocarbon oil, have high antifoaming activity. It is also observed that the preferred combinations display a very high degree of synergism that could not be predicted from a knowledge of the individual ingredients. In general, 3-component systems and 2-component systems (e.g., mineral oil plus hydrophobic filler and/or silocone surfactant) other than those already exemplified have poor antifoaming activity.

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AFl1.1 AF21.2 AF31.0 AF41.0 (a)See Table 4 for compositions.

Example 2 This example demonstrates the importance of selecting a hydrocarbon-silicone copolymer that is both soluble in the hydrocarbon oil carrier anà at the same time is surface active so as to allow the antifoam oil to spread on the foaming solution. A
series of antifoam compounds was prepared following .the methods of Example 1. All the preparations contained 6% Tullenox silica, 2.5% of an organo-silicone surfactant used in Example 1 (see Table 4), 71.5% Arcoprime 200 mineral oil and 20~ of various hydrocarbon-sllicone random copolymers of the type described in Table 2. The hydrocarbon-silicone copolymers are identified in Table 6 along with their solubility in mineral oil (at 20~) and the ability of the copolymer-mineral oil solution to spread on 0.5~ SDS. The antifoam performance of these compositions was tested by the Antifoam Performance methods set forth above. The results are shown in Table 6~ Hy~rocarbon-silicone copolymers that are both soluble and cause spreading on the SDS solution have much higher performance than copolymers that do not simultaneously satisfy D-1342~

~L22~;~1)3 these requirements. The active compositions of Table 6 would also be expecteo to be effective against other types of foams, e.g. those from proteins and nonlonic surfactants. Furthermore, Table 6 demonstrates that a broad range of copolymers are useful. For example, copolymers having pendant alkyl groups between 8 and 22 carbon atoms and with 50 to 200 dimethyl siloxane units all function well provided that the CH2 content defined by Equation 4 is ~etween about 45 and 75%.
Logically, it can be expected that copolymers outside of this molecular weight range will also function well so long as their CH2 content falls within the afore-specified percentage range. It appears that the viscosity of the copolymer is not of prime importance since some of the most effective copolymer are highly viscous while other s are low viscosity liquids.

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Example 3 The results in Table 7 demonstrate that quite different organo-silicone surfactants can function in the present antifoam co~positions provided their HLB (measured by techniques well known in the art) falls in the range disclosed above, namely 4-14 and preferably 8-11. Thus antifoams AF 22 and AF 23 were prepared with the organo-silicone surfactants set forth in Table 7, by the procedure described in Table 2. As seen in Table 7, these compositions have high antifoam performance despite the highly different structures of the two surfactants. A composition without either of the organo-silicone surfactants has a ; performance of 1.0 indicating a lack of antifoam activity in 0.5~ SDS.

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CIL. 1~ 1~5 ~r ~: cc _ ~.Z~03 Example 4 This example illustrates the use of an alternative hydrocarbon-silicone copolymer of the ABA type. An antifoam composition, AF24, was prepared by the method of Example 1 that contained 20~ of an ABA copolymer of the formula:
c~3 3( 2)17 (SitCH3)2O)21 - Si (C~2)17C~3 (12) C~3 6% Tullenox 500 silica, 2.5% of an organo-silicone surfactant as used in Example 1 (see Ta~le 4) and 71.5% Arcoprim~M200 mineral oil. When tested in 0.5% SDS at a 500 ppm level this antifoam had an efficiency of 2.9. A similar composition without the ABA copolymer had an efficiency of 1.1.
Although this particular ABA copolymer is not as effective as many o~ the random copolymers described in previous examples it did signiflcantly improve the antifoam activity of the base formulation.
Example 5 As discussed in the description of the invention other fillers besides pre-hydrophobized silica can be used in our antifoam compositlons. A
filler that is particularly convenient is hydrophilic silica that is activated in the composition by a heat tre~tment step. By way of illustration antifoams AF25 - AF31 whose compositions are set forth in Table a were prepared as follows: The hydrocarbon-silicone copolymer was first dissolved in mineral oil (ArcoprimeT~00).
CabosilT~S-5 (Cabot Corporation), a typlcal hydrophilic silica~ was dispersed in this solution .

S9(~3 with the aid of a high shear Cowles mixer.
Potassium silanolate was then added and the dispersion was transferred to a 250 ml, 3 neck flask fitted with a thermal regulator, condenser and stirrer. The mixture was heated at 150C for 2 hours under cons~ant stirring. It was observed that a large drop in viscosity took place after the heat treatment step. If desired, an organo-silicone surfactant can be addea to the antifoam compound after the heat treatment step.
The antifoam performance of compositions AF25 - AF31 was measured in several foaming solutions by the Antifoam Performance method set forth above and the results are recorded in Table 9. It is clear from the results that antifoams compounded with hydrophilic silica are particularly effective in protein (in this case fire fighting foam) based ana nonionic surfactant solutions.
It has been found that lower compounding temperatures, e.g., 75C, can be employed provided that the potassium silanolate catalyst is used.

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~ 2~:5~3 Example 6 Another useful flller is polyethylene wax, which is an example of an intrinsically hydrophobic solid. A 5.0 gm quantity of a low molecular weight polyethylene having a melting point of ll0C (from Allied Chemicals) was dispersed in a mixture consisting of 80.0 gm Arcoprime 200, 5.0 gm of the copolymer MDlooDl7 5M (C18H39) and 10-0 gm of a nonionic surfactant prepared by reacting nonyl-phenol with 4 moles of ethylene oxide. The dispersion was heated to 125C to form a homogeneous mixture. Slow cooling to room temperature yielded a fine particle dispersion of polyethylene. The resulting composition had significant antifoam activity when tested either in 0.5% TERGITOL 15-S-9 and 10% fire fighting foam.
Example 7 The influence of the ~iscosity of the hydrocarbon carrier oil on antifoam performance is shown in Table 10 for compos1tions employing prehydrophobized silica and in Table 11 for antifoams where hydrophilic silica was used.
Optimal performance is achieved when the viscosity of the carrier oil is between 16 and 75 cSt at the temperature the antifoam is used. However, good performance can be expected well outside of this viscosity range.

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~Li~2~9~3 Example 8 Varlous antifoam compositions, AF42-AF69, identified in Table 12 were prepared by procedures described in Example 1 (AF42-AF64) and Example 5 (AF65-AF69~. These composltions were emulsified in water by standard techniques using a mixture of Span 60 and Myrj 52S emulsifiers (From ICI America): 20%
emulslons were prepared. The performance of these emulsions at 200 ppm (as active) level was tested by the Antifoam Performance method set forth above and the results are collected in Table 13. It is seen that there are optimal levels of the silicone surfactant and hydrocarbon-silicone copolymer of Ca.
2.5% and 20% respectively. As was found in Table 3 with the neat antlfoam compound, superior antifoaming ability is reached with soluble hydrocarbon-silicone copolymers. It is noted that effective antifoam emulsions could ~e prepared with a range of copolymers. Finally, we note that prehydrophobized silica favors high performance in anionic surfactant solutions while hydrophilic silica activated in situ yield effective antifoams for nonionic surfactants and protein based foaming solutions.

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~L22~i~03 Example 9 This example illustrates the use of analternative hydrocarbon carrier oil, in this case, an alkyl benzene. Thus, an antifoam composition was prepared by the methods of Example 1 containing 2.5%
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(C18H37) and 71.5~ undecyl benzene. This antifoam had an efficiency of 2.6 in 0.5~ SDS when tested by the Antifoam Performance methods set forth above. The relatively lower efficiency of this composition than many of the preferred mineral oil based antifoams is probably related to its lower viscosity.
Example 10 An antifoam composition very similar to the composition of Example 9 was prepared. However, in this case, the alkylbenzene was replaced by a 1:1 mixture of kerosene and a high molecular weight polyisobutylene polymer. Such polymers are well known to be useful thickeners or "viscosifiers" for hydrocarbon oils and are used as such. The resulting antifoam had an efficiency of 21 in 0.5~
SDS when tested by the Antifoam Performance methods set forth above.
A similar antifoam in which kerosene alone was used as the oil carrier had an efficiency of 1.6 when testing unaer the same conaitions.
Example 11 The performance of several commercial antifoams tested by the Antifoam Performance methods set forth above are recorded in Table 14. On )3 comparing these results with those already given, it is seen that the novel compositions disclosed herein are génerally superior to currently available hydrocarbon oil based antifoams and compare favorably with premium quality silicone based antifoams.

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Claims (21)

1. A novel hydrocarbon oil based silicone antifoam composition comprising:
(a) from 1 to 60 weight percent of a hydrocarbon-silicon copolymer;
(b) from 1 to 20 weight percent of an hydrophobic filler having a particle size on the average of 200 to 5,000 A;
(c) from 0 to 25 weight percent of a organo-silicone surfactant of the general formula:
wherein R, R' and R" are individually alkyl groups having from 1 to 18 carbon atoms inclusive, or hydrogen, hydroxy or phenyl groups provided that no more than 5% of the total R1 R' and R" groups are hydrogen, hydroxy, phenyl or a combination thereof.
P is either a polyoxyethylene group, a polyoxypropylene group, a polyoxybutylene group or a mixture tnereof which can be terminated with elther an alkyl or hydroxyl group and L and M are such that the surfactant is liquid, has limited solubility and an HLB value of from 4-14; and x has a value of from 2 to 5 (d) from 20 to 98 weight percent of a hydrocarbon carrier oil; and (e) optionally from 0 to 20 weight percent of a silicone oil.

2. The antifoam composition of claim 1 wherein the hydrocarbon-silicon copolymer is selected from the group consisting of (a) random or block copolymers of the general formula:

(b) non-hydrolyzable ABA block copolymers of the general formula:
(c) hydrolyzable ABA block copolymers of the general formula:
(e) non-hydrolyzable ABz block copolymers of the general formula:

and (e) hydrolyzable ABz block copolymers of the general formula:

wherein R is an alkyl, aryl, aralkyl or alkaryl group containing from six to thirty carbon atoms, R', R" and R''' are individually selected from the group consisting of hydrogen or methyl, ethyl, propyl, hydroxy, and phenyl groups provided that no more than 5% of the total R', R" and R''' groups are hydrogen hydroxy, phenyl or a combination thereof, and x,y,z and n are of such a value so that the overall % CH2 content is in the range of from 30%
to 70%.

3. The antifoam composition of claim 2 wherein the hydrocarbon-silicone copolymer has a %CH2 in the range of from 45% to 65%.

4. The antifoam composition of claim 1 wherein the hydrocarbon-silicone copolymer proportion is between 5% to 20%.

5. The antifoam composition of claim 1 wherein the hydrophobic filler is selected from the group consisting of alumina, titania, silica, pearlite and clay.

6. The antifoam composition of claim 5 wherein the hydrophobic filler is silica.

7. The antifoam composition of claim 6 wherin the hydrophobic silica has been hydrophobized by either pretreatment or an in situ heating.

8. The antifoam composition of claim 1 wherein the hydrophobic filler proportion is between 2.5to 7%.

9. The antifoam composition of claim 1 wherein the silicone surfactant has an HLB of between 8 to 11.

10. The antifoam composition of claim 1 wherein the silicone surfactant proportion is between 0.5 to 10%.

11. The antifoam composition of claim 1 wherein the hydrocarbon carrier oil has a viscosity of 15 to 70 CST at the temperature for which the antifoam is used.

12. The antifoam composition of claim 11 wherein the hydrocarbon carrier oil has a viscosity of 25 to 60 CST at the temperature for which the antifoam is used.

13. The antifoam composition of claim 1 wherein the hydrocarbon carrier oil is a mineral oil.

14. The antifoam composition of claim 1 wherein up to 25 weight percent of the hydrocarbon carrier oil is replaced by an oil soluble viscosity additive.

15. The antifoam composition of claim 1 wherein the silicone oil is a polyorganosiloxane with a viscosity of from 5 to 100,000 centistokes at 25°C.

16. A novel hydrocarbon oil based silicone composition comprising:
(a) from 5 to 20 weight percent of a hydrocarbon-silicon copolymer having a % CH2 in the range of 45 to 65%;
(b) from 2.5 to 7 weight percent of a hydrophobic silica having a particle size on the average of 200 to 5,000 A;
(c) from 0.5 to 10 weight percent of a silicone surfactant having a HLB value of from 8 to 11; and (d) from 63 to 92 weight percent of a mineral oil having a viscosity of from 15 to 70 CST
at the temperature for which the antifoam is used.

17. A process for preparing the antifoam composition of claim 1 wherein the components (a) through (e) are emulsified in water employing an emulsifier to obtain an emulsion which contains from 1 to 50% of the antifoam composition.

18. The emulsion prepared according to the process of claim 17.

19. A process for defoaming a foamed solution wherein there is added to the foamed solution the antifoam composition of claim 1.

20. The process of claim 19 wherein the foamed solution contains ionic surfactants.

21. The process of claim 19 wherein the foamed solution contains nonionic surfactants.