BACKGROUND OF THE INVENTION

This invention relates to additive compositions, otherwise known as air-entraining admixtures, for incorporation in hydraulic cement mixes, such as concretes and mortars, but not limited thereto, for the purpose of increasing the durability of such mixes, after hardening, to cycles of freezing and thawing under conditions of water saturation. The increased durability of the ce entitious mix under such conditions is attained by incorporation of a system of air bubbles into the plastic mix in such a way that it will remain in the mix after hardening, and meet the specifications of resistance to freezing and thawing set forth in ASTM designation C 260. This requires that the air void system be an appropriate amount as volume percent of the hardened cementitious mass and that it have bubbles of an appropriate range of sizes and spacing parameters as determined by ASTM designation C 457. In order to attain this condition it is well known in the art to use surface agents to effect the desired air entrain ent. A number of chemical agents to achieve a desirable air entrainment are known in the art and are commercially available. Generally, these are organic chemicals having a surface active functionally at the air-water interface and fall broadly into the classes of soaps and detergents. One of the best known agents of this kind is known in the art as Vinsol resin, and is normally employed as an aqueous alkaline solution which is added to a plastic, cementitious mix, either alone or in combination with other admixtures. In the latter case, the Vinsol resin solution is separately added because of the chemical incompatibility with many other admixtures, due to the fact that the pH and the presence of calcium and various other ions renders insoluble the al ali-neutralized acids comprising Vinsol resin. Thus, Vinsol resin is the sodium soap of specific resin acids derived by solvent extraction from pine stumps. It is also known in the art

to employ various anionic and nonionic surfactants broadly in the detergent class to effect a desirable kind and degree of air entrainment in cementitious mixes. Thus, U.S. Patent 4,249,948 discloses the use of an alpha olefin sulfoπate with a water reducing agent wherein the former acts as an air-entraining agent in a hydraulic cement composition.

Materials described above generally and historically have been satisfactory for their intended use. However, recent changes in concrete technology have caused an increase in instances of unsatisfactory performance. A significant change in concrete technology is employment of pozzolanic materials as additions or more commonly as partial substitutes for a portion of the portland cement on a larger scale than hitherto. In particular, fly ash, a by-product of coal combustion in the generation of electric power, is finding increasing usage as a pozzolanic cement substitute. The composition of fly ashes is determined by the nature of the coal burned and the combustion conditions but generally they are alu inosilicate glasses with varying amounts of iron oxide, alkali and alkaline earth cations and residual uπburned carbon. Certain ones, rich in calcium ions, may be not only pozzolanic in nature but may possess some cementitious qualities inherently, because of their mineralogical composition, such as the presence of tricalcium aluminate. However, it is the residual carbon content which is generally considered to be associated with the increased incidence of failure of the known air entraining agents to perform in a desirable manner. These failures include the need to use higher dosages of admixtures known in the art, and even more troublesome, a tendency to either lose air, or to uncontrollably increase in air content, as mixing time is extended. Associated with this loss of air is a loss in workability as measured by the slump cone in accordance with the American Society for Testing and Materials (ASTM) designation C 143.

Thus, there exists the continuing need to discover surface active agents, or combinations of such agents, that will overcome the problem described above.

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SUMMARY OF THE INVENTION

The present invention is an additive composition for incorporation in hydraulic cement mixes, such as normal concretes, mortars and grouts and neat cement mixes, with optional replacement of a portion of the hydraulic cement of said mixes with a corresponding amount of pozzolanic material, and the resulting improved cementitious mixes and process for incorporating the additive composition.

For purposes of this invention the term "hydraulic cement" is intended to mean and to include all cementitious compositions based primarily on silicates capable of being set and hardened by the action of water, such as port!and cements, sulfate-resisting cements, blast furnace cements and pozzolanic cements, but the preferred use of the present additive composition is in port!and cement mixes and such mixes when a portion of the port!and cement has been replaced by fly ash. The term "port!and cement" is intended to include all cementitious compositions which have a high content of tricalcium silicate, conforming with the specifications set forth in ASTM designation C-150, and the Portland blended cements such as those described in ASTM C-595. Broadly, the invention comprises a hydraulic cement mix including hydraulic cement, aggregate, sufficient water to effect hydraulic setting of the cement, and an additive comprising a mixture of the soluble alkanolamine and alkali salts of fatty acids plus the soluble alkali and alkanolamine salts of certain sulfonic acids such as alpha olefin sulfonic acids plus a third nonionic component such as the fatty acid amides and polyethylene glycol derivatives as well as selected other components, as more fully described hereafter. While these materials may be added in combination in their normal state to a cementitious mix it is most convenient to add them as a single aqueous solution which may have a desired cosmetic coloring agent and if the water employed is not distilled or "deionized" so as to be essentially free of alkaline earth cations, the necessary amount of a chelating agent for these ions may also be added so as to

maintain the additive components tn solution. The sodium salt of nitrilotriacetic acid is one example of such a chelating agent. The effect of the additive to entrain a desirable amount and kind of air void system in a variety of cementitious mixes and particularly in mixes containing fly ash having a relatively high carbon content as indicated by an ignition loss of up to 62 or more by weight of fly ash, when the cementitious system is subjected to prolonged mixing up to the order of one hour, was found to depend optimally on the presence of all three of the components described above, although in certain instances combination of two of the three components may produce desirable effects. Thus, the fatty acid salts of soaps which are known as such in the art under prolonged mixing in a cementitious system require relatively high dosages, entrain air slowly, and have a tendency to gain air with extended mixing. The sulfonic acid salts employed alone in cementitious mixes, on prolonged mixing, tend to progressively lose the air which they first entrain. The polyethylene glycol or other nonionic component may or may not of itself be an air-entraining agent in cementitious mixes. However, the unexpected and πonobvious result obtained by employing these three materials in combination in a cementitious system undergoing extended mixing is to yield with a favorable dosage response an excellent air void system stable in the plastic cementitious system and having a desirable improved size and distribution in the cementitious system after hardening.

It is therefore an object of the present invention to provide improved air-entrained hydraulic cement mixes.

It is another object of this invention to provide improved air-entrained hydraulic cement mixes, including concrete, mortar and grout mixes, neat cement and dry mixes, which include an additive composition that will advantageously entrain an air void system having desired characteristics when said additive is employed over a relatively wide dosage range, or have a superior dosage response relative to functionally similar additives known in the art.

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DESCRIPTION OF THE PREFERRED EMBODIMENTS

The fatty acid salts of the instant invention may be represented by the following formula:

RCOOM ^" where R is an alkyl chain that may be branched or unbranched, saturated or unsaturated, but wherein the number of carbon atoms is in the range from about 12 to about 24, and M is an alkali metal, with sodium or potassium being preferred. Optionally, the fatty acid may be neutralized with triethanolamine so as to produce the triethanolamine salt of the fatty acid, or other alkanolamines may be so employed. The portion of this component in the three-component additive may range from a minimum of about 50% to a maximum of about 90% by weight based on dry solids or 100% active materials. The salts of the sulfonic acids having a carbon chain length of 12 to 24 may be represented by the following general formula:

RS0 ₃ M where R is an alkyl or an alkylaryl group in which the alkyl group may be branched or unbranched and saturated or unsaturated with a number of carbon atoms in the range indicated above for the fatty acid salts and M has the same meaning as described above. Optionally, anionic sulfates may be used. The proportion of this component in two- or three-component additives may vary from 0% to about 25% by weight, based on dry solids or 100% active material.

The preferred nonionic ingredient is a polyethylene glycol deriative which may be represented by the following general formula: where n is an integer ranging from about 3 to about 30 and R is selected from a group comprising hydrogen, a fatty acid ester, an alkyl or an alkylaryl group. The proportion of this component in the additive of this invention may range from about 0 to about 25% by weight, based on dry solids or 100% active material. Optionally, other nonionic components such as fatty acid amides may be used.

In sumπary the present invention comprises a set of three-component additives comprising up to about 25% sulfonates with 12 to 14 carbon chain length plus from about 0% to about 25% nonionic component and the remainder being a salt of a fatty acid, all on a dry solids basis, and a set of two-component additives of like proportions except that the sulfonic acid salt is absent. In either case the additive is incorporated into a cementitious mix from about .002% to about .06% based on dry solids or 100% active ingredients with respect to total cementitious material. The two-component subsystem obtained when the nonionic component is absent is also useful. In this context the term cementitious material means portland cement plus pozzolanic addition, if any. The pozzolanic additions may be slag as well as fly ash. In the practice of the present invention the additive is incorporated into hydraulic cement mixes such as portland cement concretes and mortars in amounts sufficient to yield an entrained air void system of the proper amount and quality after extended mixing in the plastic state. As a practical matter the additive is incorporated into the mix as an aqueous solution, which may be of any convenient concentration.

The additive may be incorporated into the mix as a portion of the mix water, but it may also be incorporated in any other convenient manner, including adding it to the dry mix before the water s incorporated therein.

The term aggregate is intended to include both fine aggregate, such as sand, and coarse aggregate, such as crushed stone or gravel, as in common in the art. In general for mortars, the aggregate may be sand or other fine aggregate meeting the requirements of ASTM standard C-33. The proportions of fine and coarse aggregate will vary depending upon the desired use and properties of the mortar or concrete. For most uses, although not limited thereto, the size of the fine aggregate will be within the broad range of about +4 mesh to -100 mesh U.S. Standard Sieve (ASTM C-ll), while the size of the coarse aggregate will be within the broad range of 3 inches (7.6 cm) to

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4 mesh. The coarse aggregate will usually be of mineral origin, such as gravel or crushed rock, but it may in some instances consist at least partially of graded metallic materials such as crushed iron borings, or it may be a manufactured aggregate, such as a slag.

For both mortars and concretes, the amount of water employed generally would be enough to effect hydraulic setting of cementitious material in the mix and to provide suitable workability in the plastic state. This would broadly range from about 20% to 60% by weight of the cementitious materials in mortars and about 25% to 70% by weight of the cementitious material in concrete mixes. The precise proportion of water will depend on the end use of the cementitious mix as well as on its composition. For the purpose of illustrating the advantageous results obtainable by the practice of the present invention, plain concrete mixes were prepared and compared to similar mixes containing the additives of the present invention and functionally similar additives previously known. Since there are no standard test methods to demonstrate in the laboratory the loss of air or undesirable gain in air content on extended mixing of concretes containing air entraining agents, it was necessary to devise a procedure that is considered to be representative of practice in the field. The sequence of operations in this procedure are: preparation of concrete mixes with a nominal slump of 5 to 6 inches (10.2 to 12.7 cm) and an air content of 6.0 _+ 1.0% by volume of the concrete. Each mix was designed for a total of 517 lbs/yd ³ (307 Kg/m ³ ) to 600 lb/yd ³ (356 Kg/m ) of cementitious material with either portland cement alone or with a combination of portland cement and fly ash, with the latter substituted for 22% or greater of the cement by weight. The concrete, with an appropriate amount of water to attain the specified slump value is then mixed in a mixer of 2 cubic feet (.057 m ) capacity at 20 revolutions per minute for 3 or 5 minutes. Next, specimens are taken for subsequent determination of parameters of the air void system after

hardening when desired and the initial air content is determined by the pressure meter method as described in ASTM standard test method C-231 and the slump value which is an index of workability is determined in accordance with ASTM standard method C-143. Next, agitation is continued at a reduced rate to simulate practice in the field wherein there are delays and variable delivery times, as is discussed in ASTM designation C-94, until about 30 minutes have elapsed. Then, slump and air content are again determined and the material is mixed for an additional 2 minutes. This process is repeated until about 1 hour after initial mixing has elapsed, at which time air content is again determined and additional water is added to restore initial slump. The concrete is mixed for 3 minutes, and air content is again determined. Thus the experiment is terminated at about 67 minutes after the beginning of initial mixing. The retempering by water addition at the final mixing period to restore desired slump follows field practice. It is the air content at this point which is vital to the concrete durability after hardening. In Table I below are shown data, obtained as outlined above, at an ambient temperature of 72 ^β F (22 ^β C) and the cementitious material being portland cement only in the proportion of 517 lb/yd ³ (307 Kg/m ³ ), illustrating the problem of progressive air loss with extended mixing. Dosages of the air entraining additives are on a 100% solids or active basis, as weight percent to cementitious material. Initial slump was about 5 inches (12.7 cm).

TABLE I

Sodium Alpha

Admixture Vinsol Resin Olefin Sulfonate Admixture dosage, % .0061 .00169

Initial Air Content, Vol .% 5.8 5.9 Air, After 1/2 hr. mixing 4.6 4.8 Ai r, after 1 hr. mixi ng 3.4 4.0 Air, after sl ump restored 3.3 3.5

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The desired air content after slump restoration is a value close to the initial 5.8 volume percent. It is apparent that the air loss with extended mixing and use of Vinsol resin is very significant. Use of one component of the present invention, the sodium alpha olefin sulfonate, somewhat improves air retention, but still, to a lesser extent than is desired.

A combination of the foaming surfactant, sodium alpha olefin sulfonate, and a nonionic agent, in this case, the 1:1 molar reaction product of cocamide-diethanolamine, (DEA), when tested in a plastic concrete mix in the manner described above, and results were secured as shown in Table II.

TABLE I I

Sodi urn Alpha

Ol efi n Sul fonate pl us Coca i de

DEA i n 5 :1

Admixture Vinsol Resin Wei ght Ratio Admixture Dosage, % .0069 .0016 Initial Air Content, Vol .% 5.8 5.6 Air, after 1/2 hr. mixing 5.2 4.6 Air, after 1 hr. mixi ng 3.5 4.1 Air, after slump restored 3.3 3.7

It i s apparent that the combination of foami ng surfactant and the nonionic agent, as shown above, somewhat further benefits air retention, but stil l , not to the extent desi red. However, when the soap of a l ow rosin tal l oil fatty acid, i s added to make a three-component air-entraining admixture, and simil ar tests are made, results are remarkable and unexpected, as shown by data i n Tabl e III bel ow.

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TABLE III

Air

Dosage Initial Air, w/ Air w/ after

Wt.% of Air 30 min. 60 min. slump cementit. Content mixing mixing restor.

No. Admixture component Vol.% Vol.% Vol.% Vol.%

1. Vinsol Resin .0071 5.5 4.0 2.8 2.5 2. A0S ⁽¹⁾ +CD ⁽²⁾ - ¥ FA< ³ > Wt. Ratio:

1:1/2:6-1/4 .0070 6.0 7.5 6.8 6.6

3. AOS+CD+FA, Wt. ratio:

1:1:6-1/4 .0075 6.0 7.8 6.0 6.8

4. AOS+CD+FA, Wt. Ratio:

1:2:6-1/4 .00685 6.0 8.0 7.1 7.0

(1) Alpha olefin sulfonate, sodium salt.

(2) cocami de-diethanol a iπe reaction product, described above.

(3) the tall oil fatty acid soap, described above

The very beneficial results illustrated in Table III were unexpected and were shown by further experiments to be due to a synergistic interaction of the three components of the air-entraining agents as shown below, in Tables IV, V, and VI. In this case, the experimental conditions described above were employed except that instead of whole concrete, a mortar simulating the mortar fraction of corresponding whole concrete was employed. That is, since air entrainment occurs wholly within the mortar fraction, removal of aggregate accentuates the effects being measured.

The shorthand symbols defined above are shown in the tables and have the same meaning except that the cocamide-diethanolamine (DEA) reaction product is derived from a 1:2 molar ratio of reactants instead of a 1:1 molar ratio. It is still properly designated a cocamide DEA product, however.

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TABLE IV

Initially

Dose, Wt. % Entrained air,

No. Admi xture of Cement Vol. %

1. FA .01 2

2. AOS .0016 2

3. CD .0032 2

4. No. l+No.2+No.3 .0148 14

Since 14 is significantly greater than 2 plus 2 plus 2, synergism is strongly indicatted by data in Table IV. Note that component CD, although used at twice the dosage of AOS entrains only equal air.

TABLE V

Initially

Dose, Wt. % Entrained air,

No. Admixture of Cement Vol. %

1. AOS .0023 4

2. CD .0046 4

3. No.l+No.2 .0069 14

Since 14 is significantly greater than 4 plus 4, data in

Table V indicate a synergistic interaction in this two-component subsystem, with respect to air-entrainiπg efficiency. Note that again the CD component must be employed at twice the dosage of the AOS component to entrain the same amount of air.

TABLE VI

Initially

Dose, Wt. % Entrained air,

No. Admi xture of Cement Vol. %

1. FA .0170 3

2. CD .0054 5

3. No.l+No.2 .0224 14

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Since 14 is significantly greater than 3 plus 5, data of Table VI indicate a synergistic interaction of the FA and CD components, with respect to air-entraining efficiency.

Further experimentation revealed that in this type of three-component air-entraining admixture, namely, a combination o-f a fatty acid soap, a foaming detergent and a nonionic agent as described above7 that another type of nonionic agent of the class of which polyethylene glycol is an example, function in the same manner. Experiments were conducted as shown below in Table VII, employing a polyethylene glycol with an average molecular weight of 400. The experimental conditions were the same as previously described except that more severe conditions were imposed. Cement was replaced in the concrete mix by 22% of its weight with a fly ash that normally aggravates air loss on prolonged mixing of the plastic mix. The total cementitious component, that is, cement plus fly ash, was 517 lb/yd ³ (307 kg/m ³ ). In Table VII, the polyethylene glycol is designated PEG and the other two components are designated AOS and FA, as previously defined.

TABLE VII

Air

Dosage Initial Air, w/ Air w/ after Wt.% of Air 30 mi n. 60 mi n. s ump cementit. Content mixi ng mixi ng restor.

No. Admixture component Vol . % Vol . % Vol . % Vol .% 1. FA+PE6+A0S

Wt.Ratio:

.75:.125:.125 .0335 6.1 6.7 7.0 6.6

2. FA+AOS Wt. Ratio:

.86:.17 .0269 5.9 6.4 6.2 5.2

3. FA+AOS+CD Wt. Ratio:

.75: .125: .125 .0285 6.3 6.7 6.7 5.8

Data in Table VI I show, in compari ng Mix No. 1 and Mix No. 3, that the polyethyl ene glycol may be substituted for the

cocamide-diethanolamine adduct in three-component mixes, with the same component ratios and essentially the same total dosage, namely about .03 weight percent of cementitious material, and similar beneficial effects of retain ent of entrained air are secured. Omission of the nonionic component, as shown in Mix No. 2, still results in a desirable result with use of the other two components, but not quite to the same degree.

Further experiments, conducted under the same conditions as described above to secure data for Table VII, led to results shown in Table VIII below. These data give insight into why combinations of components are necessary and also show that foaming detergents other than AOS can beneficially be used. The particular one shown in Table VIII is the sodium salt of dodecyl benzene sulfonic acid, where the alkyl chain is linear, and is designated DBS. Other components are indicated by symbols defined above.

TABLE VIII

Air

Dosage Initial Air, w/ Air w/ after

Wt.% of Air 30 mi n. 60 min. sl ump cementit. Content mixi ng mi xi ng rest or

No. Admi xture component Vol . % Vol . % Yol . % Vol .%

1. FA+PEG+DBS wt. ratio: .0300 6.3 6.8 7.1 6.9

.75 : .125 : . 125

2. FA .0503 6.0 7.4 8.1 7.3

3. AOS .0093 6.3 2.6 2.0 1.1

In the table above, Mix No. 1 indicate that alkylaryl sulfonate salts may advantageously be employed as the foaming detergent component of the three-component admixture. Data for Mix No. 2 indicates the disadvantages of using the fatty acid salt or soap component alone, namely that a high dosage is required to secure the initial air content desired, namely about 6 volume percent, and that there s a tendency to gain air with increased mixing. Data for Mix No. 3 show the disadvantages of

employing the foaming surfactant type of air entraining agent alone, namely, that while it readily entrains the initially desired air content with a low dosage rate, it quickly loses this air with continued mixing.

The high foaming anionic detergent described above and illustrated by alkanolamine and alkali salts of sulfonic acids may be replaced by functionally similar alcohol sulfates and ethoxylated alcohol sulfates as illustrated by data in Table IX below. In this case DBS as defined above is replaced by sodium laureth 12 sulfate, designated LS. The other symbols have the same meaning earlier described. In addition the nonionic component may be ethoxylated alkylphenol, shown in Table IX as EAP. The same conditions as previously described for the fly-ash containing mixes were employed.

TABLE IX

Air

Dosage Initial Air, w/ Air w/ after

Wt.% of Air 30 min. 60 min. sl ump cementit. Content mixi ng mixi ng restor

No. Admixture component Vol .% Vol .% Vol .% Vol .%

1 . FA+PEG+LS Wt. Ratio

.75: .125: .125 .0205 5.7 6.3 5.4 5.2

2. FA+EAP+AOS Wt. Ratio

.75: .125: .125 .0138 6.0 6.1 5.8 6.0

While the invention has been described with reference to certain preferred embodiments thereof, those skilled in the art will appreciate that various modifications and substitutions can be made without departing from the spirit of the invention. In particular in the context of this invention aqueous solutions of the components described may have added thereto small amounts of compatible chelating agents for alkaline earth cations such as magnesium or calcium which normally occur in ordinary water but which would tend to precipitate the surface active agents herein

described. Also, smal l amounts of compatible cosmetic coloring agents may be added. It is intended that the invention will be l imited only by the scope of the claims which follow: