Azeotropic and pseudoazeotropic blends

Abstract

The present invention relates to azeotropic blends and pseudoazeotropic blends and to coating compositions including such blends. In one aspect, an azeotropic blend or a pseudoazeotropic blend consists essentially of hexamethyldisiloxane and a second component selected from the following: isobutanol, n-propyl acetate, n-butanol, and 1-methoxy-2-propanol.

Claims

1. A coating composition comprising: an azeotropic blend or a pseudoazeotropic blend consisting essentially of hexamethyldisiloxane and a second component selected from the following: isobutanol, n-propyl acetate, n-butanol, and 1-methoxy-2-propanol; and an acrylic resin or epoxy resin, wherein the coating composition contains 50 to 80 wt % of hexamethyldisiloxane when the second component is isobutanol, n-butanol, or 1-methoxy-2-propanol, and wherein the coating composition contains 20 to 50% wt % of hexamethyldisiloxane when the second component is n-propyl acetate, the wt % calculated against the total weight of hexamethyldisiloxane and the second component.

2. The coating composition of claim 1, wherein the second component is isobutanol.

3. The coating composition of claim 1, wherein the second component is n-propyl acetate.

4. The coating composition of claim 1, wherein the second component is n-butanol.

5. The coating composition of claim 1, wherein the second component is 1-methoxy-2-propanol.

6. A method of forming a coating composition, comprising: blending an acrylic resin or epoxy resin with an azeotropic blend or a pseudoazeotropic blend comprising hexamethyldisiloxane and a second component selected from the following: isobutanol, n-propyl acetate, n-butanol, and 1-methoxy-2-propanol, wherein the coating composition contains 50 to 80 wt % of hexamethyldisiloxane when the second component is isobutanol, n-butanol, or 1-methoxy-2-propanol, and wherein the coating composition contains 20 to 50% wt % of hexamethyldisiloxane when the second component is n-propyl acetate, the wt % calculated against the total weight of hexamethyldisiloxane and the second component.

7. The method of claim 6, further comprising applying the coating composition as a paint or coating.

Description

DETAILED DESCRIPTION

(1) As used herein, “a,” “an,” “the,” “at least one,” and “one or more” are used interchangeably.

(2) The terms “comprising,” “including,” “having,” and their derivatives, are not intended to exclude the presence of any additional component, step or procedure, whether or not the same is specifically disclosed. In order to avoid any doubt, all compositions claimed through use of the term “comprising” may include one or more additional compounds unless stated to the contrary. In contrast, the term, “consisting essentially of” excludes from the scope of any succeeding recitation any other component, step, or procedure, excepting those that are not essential to operability. The term “consisting of” excludes any component, step, or procedure not specifically delineated or listed. The term “or”, unless stated otherwise, refers to the listed members individually as well as in any combination. Use of the singular includes use of the plural and vice versa.

(3) Also herein, the recitations of numerical ranges by endpoints include all numbers subsumed in that range (e.g., 1 to 5 includes 1, 1.5, 2, 2.75, 3, 3.80, 4, 5, etc.). For the purposes of the invention, it is to be understood, consistent with what one of ordinary skill in the art would understand, that a numerical range is intended to include and support all possible subranges that are included in that range. For example, the range from 1 to 100 is intended to convey from 1.01 to 100, from 1 to 99.99, from 1.01 to 99.99, from 40 to 60, from 1 to 55, etc.

(4) Unless stated to the contrary, implicit from the context, or customary in the art, all parts and percents are based on weight and all test methods are current as of the filing date of this disclosure.

(5) “Azeotropic” and like terms mean a blend of two or more components that boil or distill as a single component at a given temperature and pressure while the liquid and the vapor concentrations are the same. “Pseudo-azeotropic” and like terms mean a blend of two or more components that boils or evaporates closely, but not exactly, like a single component, i.e., the solvent system sufficiently approximates an azeotropic system so as to allow it to be used as an azeotropic system. Both azeotropic and pseudo-azeotropic blends have boiling points lower than either of the pure components used in the blend. Unless stated otherwise herein, the determination of whether a blend is azeotropic or pseudo-azeotropic is based on boiling points at 720 mm mercury (mm Hg).

(6) “Solvent” and like terms mean a substance that is capable of dissolving another substance (i.e., a solute) to form an essentially uniformly dispersed mixture (i.e., solution) at the molecular or ionic size level.

(7) “Hydrocarbon” and like terms mean a compound consisting only of carbon and hydrogen atoms.

(8) “Solution” and like terms mean a homogeneous composition that is (1) variable, i.e., can exist in different concentrations of solute in solvent, (2) all but one component is present in simplest units, e.g., molecules, and (3) can be separated by physical methods into two or more pure substances. In the context of this invention, solution refers to liquid compositions.

(9) “Composition” and like terms mean a mixture or blend of two or more components.

(10) Embodiments of the present invention generally relate to azeotropic blends or pseudoazeotropic blends consisting essentially of hexamethyldisiloxane and a second component selected from the following: isobutanol, n-propyl acetate, n-butanol, and 1-methoxy-2-propanol.

(11) In some embodiments, the azeotropic blend or pseudoazeotropic blend consists essentially of hexamethyldisiloxane and isobutanol. In some embodiments, the blend consists of hexamethyldisiloxane and isobutanol. The boiling point of the blend, in some embodiments, is less than the boiling point of hexamethyldisiloxane and less than the boiling point of isobutanol at 720 mm Hg. In some such embodiments comprising isobutanol, the blend comprises 50 to 80 weight percent hexamethyldisiloxane based on the total weight of the blend.

(12) In some embodiments, the azeotropic blend or pseudoazeotropic blend consists essentially of hexamethyldisiloxane and n-propyl acetate. In some embodiments, the blend consists of hexamethyldisiloxane and n-propyl acetate. The boiling point of the blend, in some embodiments, is less than the boiling point of hexamethyldisiloxane and less than the boiling point of n-propyl acetate at 720 mm Hg. In some such embodiments comprising n-propyl acetate, the blend comprises 20 to 50 weight percent hexamethyldisiloxane based on the total weight of the blend.

(13) In some embodiments, the azeotropic blend or pseudoazeotropic blend consists essentially of hexamethyldisiloxane and n-butanol. In some embodiments, the blend consists of hexamethyldisiloxane and n-butanol. The boiling point of the blend, in some embodiments, is less than the boiling point of hexamethyldisiloxane and less than the boiling point of n-butanol at 720 mm Hg. In some such embodiments comprising n-butanol, the blend comprises 50 to 80 weight percent hexamethyldisiloxane based on the total weight of the blend.

(14) In some embodiments, the azeotropic blend or pseudoazeotropic blend consists essentially of hexamethyldisiloxane and 1-methoxy-2-propanol. In some embodiments, the blend consists of hexamethyldisiloxane and 1-methoxy-2-propanol. The boiling point of the blend, in some embodiments, is less than the boiling point of hexamethyldisiloxane and less than the boiling point of 1-methoxy-2-propanol at 720 mm Hg. In some such embodiments comprising 1-methoxy-2-propanol, the blend comprises 50 to 80 weight percent hexamethyldisiloxane based on the total weight of the blend.

(15) Embodiments of the present invention also relate to coating compositions. A coating composition of the present invention comprises any of the azeotropic blends or pseudoazeotropic blends disclosed herein.

(16) Blends

(17) Blends according to embodiments of the present invention advantageously behave as azeotropes or pseudoazeotropes. The azeotropic blends and pseudoazeotropic blends of the present invention consist essentially of, or consist of, a first component and a second component. The first component is hexamethyldisiloxane. The second component is isobutanol, n-propyl acetate, n-butanol, or 1-methoxy-2-propanol. The first and second components form the blend. The blend can be used as a solvent in some embodiments. Thus, some embodiments of the present invention relate to solvents that consist essentially of, or consist of, hexamethyldisiloxane and a second component selected from the following: isobutanol, n-propyl acetate, n-butanol, and 1-methoxy-2-propanol.

(18) The first component in the blend is hexamethyldisiloxane. Hexamethyldisiloxane is commercially available from The Dow Chemical Company as XIAMETER™ PMX-200 silicone fluid, 0.65 cSt (centistokes). As set forth further herein, the amount of hexamethyldisiloxane used in embodiments of the present invention depends on the second component used (e.g., isobutanol vs. n-propyl acetate vs. n-butanol vs. 1-methoxy-2-propanol).

(19) In some embodiments, the second component is isobutanol. Isobutanol is commercially available from a variety of manufacturers. In some such embodiments, the blend or solvent consists essentially of hexamethyldisiloxane and isobutanol. In some such embodiments, the blend or solvent consists of hexamethyldisiloxane and isobutanol. In embodiments where the second component is isobutanol, the blend comprises 50 to 80 weight percent hexamethyldisiloxane based on the total weight of the blend. The blend or solvent, in some embodiments, consists essentially of 50 to 80 weight percent hexamethyldisiloxane and 20 to 50 weight percent isobutanol, based on the total weight of the blend. The blend or solvent, in some embodiments, consists of 50 to 80 weight percent hexamethyldisiloxane and 20 to 50 weight percent isobutanol, based on the total weight of the blend.

(20) In some embodiments, the second component is n-propyl acetate. n-propyl acetate is commercially available from a variety of manufacturers. In some such embodiments, the blend or solvent consists essentially of hexamethyldisiloxane and n-propyl acetate. In some such embodiments, the blend or solvent consists of hexamethyldisiloxane and n-propyl acetate. In embodiments where the second component is n-propyl acetate, the blend comprises 20 to 50 weight percent hexamethyldisiloxane based on the total weight of the blend. The blend or solvent, in some embodiments, consists essentially of 20 to 50 weight percent hexamethyldisiloxane and 50 to 80 weight percent n-propyl acetate, based on the total weight of the blend. The blend or solvent, in some embodiments, consists of 20 to 50 weight percent hexamethyldisiloxane and 50 to 80 weight percent n-propyl acetate, based on the total weight of the blend.

(21) In some embodiments, the second component is n-butanol. n-butanol is commercially available from a variety of manufacturers. In some such embodiments, the blend or solvent consists essentially of hexamethyldisiloxane and n-butanol. In some such embodiments, the blend or solvent consists of hexamethyldisiloxane and n-butanol. In embodiments where the second component is n-butanol, the blend comprises 50 to 80 weight percent hexamethyldisiloxane based on the total weight of the blend. The blend or solvent, in some embodiments, consists essentially of 50 to 80 weight percent hexamethyldisiloxane and 20 to 50 weight percent n-butanol, based on the total weight of the blend. The blend or solvent, in some embodiments, consists of 50 to 80 weight percent hexamethyldisiloxane and 20 to 50 weight percent n-butanol, based on the total weight of the blend.

(22) In some embodiments, the second component is 1-methoxy-2-propanol. 1-methoxy-2-propanol is commercially available from The Dow Chemical Company as DOWANOL™ PM. In some such embodiments, the blend or solvent consists essentially of hexamethyldisiloxane and 1-methoxy-2-propanol. In some such embodiments, the blend or solvent consists of hexamethyldisiloxane and 1-methoxy-2-propanol. In embodiments where the second component is 1-methoxy-2-propanol, the blend comprises 50 to 80 weight percent hexamethyldisiloxane based on the total weight of the blend. The blend or solvent, in some embodiments, consists essentially of 50 to 80 weight percent hexamethyldisiloxane and 20 to 50 weight percent 1-methoxy-2-propanol, based on the total weight of the blend. The blend or solvent, in some embodiments, consists of 50 to 80 weight percent hexamethyldisiloxane and 20 to 50 weight percent 1-methoxy-2-propanol, based on the total weight of the blend.

(23) Blends or solvents according to embodiments of the present invention can be prepared using techniques known to those of skill in the art based on the teachings herein.

(24) Coating Compositions

(25) Some embodiments of the present invention relate to coating compositions. Coating compositions of the present invention comprise, in various embodiments, any azeotropic blend or pseuodoazeotropic blend disclosed herein. The azeotropic and pseudoazeotropic blends can be solvents in such coating compositions.

(26) Examples of coating compositions that can incorporate an azeotropic blend or pseudoazeotropic blend of the present invention as a solvent include, without limitation, paints (e.g., house paints, asphalt paints, industrial paints, etc.), paints used to coat metal, and other coatings. For example, the azeotropic and pseudoazeotropic blends can be used to replace other solvents typically used in such coating compositions (e.g., paints) such as p-chlorobenzotrifluoride (PCBTF), n-butyl acetate, methyl acetate, acetone, toluene, and others.

(27) Persons of ordinary skill in the art can readily modify typical coating compositions to incorporate the inventive azeotropic or pseudoazeotropic blends as solvents based on the teachings herein. In addition to solvent, typical coating compositions also include polymeric binders, pigments, and other additives. Examples of such coating compositions can be found in W. Finzel, “Volatile Methylsiloxanes as Exempt Solvents in Protective Coatings”, J. of Coatings Technology, Vol. 68, No. 852, pp. 69-72 (January 1996); US Patent Publication No. 2018/0148605; US Patent Publication No. 2014/0065432 and Product Bulletin from Reichhold for Beckosol 10-060.

(28) Coating compositions of the present invention can be prepared using techniques known to those having ordinary skill in the art based on the teachings herein.

(29) Some embodiments of the invention will now be described in detail in the following Examples.

EXAMPLES

(30) The following examples are given to illustrate the invention and should not be construed as limiting its scope. All parts and percentages are by weight unless otherwise indicated.

(31) A number of components are blended with hexamethyldisiloxane. The hexamethyldisiloxane used is XIAMETER™ PMX-200 silicone fluid, 0.65 cSt (centistokes) from the Dow Chemical Company. The components evaluated as part of a binary blend with hexamethyldisiloxane are: isobutanol, methyl isobutyl ketone (MIBK), propyl acetate and isobutyl acetate (all from the Aldrich Chemical Company), and n-butanol and 1-methoxy-2-propanol (DOWANOL™ PM) both from The Dow Chemical Company).

(32) Boiling Point Measurements

(33) The boiling measurements of the pure components and the blends are measured as follows. In a typical experiment, 15 grams of the pure solvent or solvent blend to be tested is added to a single neck, 50 mL round bottom flask equipped with a built-in thermocouple well. A small Teflon stir bar is added to the flask and the flask is secured on a ring stand with a clamp. A heating mantle is attached to the flask and a magnetic stir plate is placed beneath the mantle. Control and high limit thermocouples leading from a digital temperature controller are placed between the mantle and the flask. Another thermocouple is placed inside the thermocouple well. A condenser is attached to the flask and an adapter leading to a nitrogen-vacuum line is placed on the condenser. The stir plate is turned on low speed. Dry ice is added to the vacuum trap and the vacuum pump turned on. The pressure is adjusted to the desired value by means of a Tescom backpressure regulator and nitrogen flow from a 5 psig nitrogen line. The pressure is read with a digital Rosemount gauge. The system had a relief valve in place so that over pressurization would not occur. The pressure in the apparatus is initially reduced to about 10 mmHg and then increased to about 760 mmHg with nitrogen. After this initial purging of air, the pressure is set to 720 mm Hg. The temperature controller is turned on and the mantle temperature increased gradually in small increments until the liquid in the flask is observed to boil and a reflux is established. The temperature of the boiling liquid measured at the thermocouple well is recorded as the boiling point.

(34) The boiling points of the neat XIAMETER™ PMX-200 fluid and of the neat second solvent (second component) of interest are measured before measuring the boiling point of blends. Blends are made up with the following weight percent compositions: 80/20 XIAMETER™ PMX-200 fluid (24.00±0.03 g) and second solvent (6.00±0.03 g); 50/50 XIAMETER™ PMX-200 fluid (15.00±0.03 g) and second solvent (15.00±0.03 g); and 20/80 XIAMETER™ PMX-200 fluid (6.00±0.03 g) and second solvent (24.00±0.03 g). Each blend made is labeled and stirred briefly to achieve solubility. For the boiling point determination, 15.00±0.03 g of blend was used.

(35) The results are shown in Table 1.

(36) TABLE-US-00001 TABLE 1 Boiling Boiling Point (° C.) of Point of XIAMETER ™ PMX-200 Second blend at Given Weight % of Second Component Component XIAMETER ™ fluid (Second Solvent) (° C.) 100% 80% 50% 20% Iso-butanol 107 99 91* 93*  99 Methyl isobutyl ketone 114 99 99  102  106 Propyl acetate 96 99 95* 95*  95* Isobutyl acetate 116 99 100  104  109 n-butanol 117 99 94* 97* 105 1-methoxy-2-propanol 119 99 95* 97* 104
The blends marked with an asterisk (*) represent inventive azeotropic blends according to some embodiments of the present invention.
Solubility of Acrylic and Epoxy Resins in the Inventive Azeotropic Blends

(37) To demonstrate the potential use of the inventive azeotropic blends in coating formulations, their compatibility with three common resins is evaluated at a theoretical concentration of 10% resin (weight of resin per volume of solvent, w/v). The resins used are: PARALOID™ B-66 100% acrylic resin (The Dow Chemical Company), PARALOID™ B-72 100% acrylic resin (The Dow Chemical Company), and DER® 331 epoxy resin (Olin Corporation). The resin (0.50±0.03 g) is weighed into a 16 mL vial, and 5.0 ml of the specified azeotropic blend is pipetted into the vial, which is then capped with a polyethylene-lined lid and labeled appropriately. This procedure is repeated with each of the resins and the azeotropic blends evaluated. The vials are placed in an Eberbach shaker on low setting. After 24 hours, the vials are removed from the shaker and allowed to sit on a lab bench for 30 minutes before they are visually rated as soluble or insoluble. The ratings are summarized in Table 2.

(38) TABLE-US-00002 TABLE 2 PARALOID ™ B-66 PARALOID ™ B-72 DER ™ 331 Azeotropic Composition (10% by wt.) (10% by wt.) (10% by wt.) 50% XIAMETER ™ PMX-200 Soluble Insoluble Soluble 50% n-propyl acetate 20% XIAMETER ™ PMX-200 Soluble Soluble Soluble 80% n-propyl acetate 50% XIAMETER ™ PMX-200 Soluble Insoluble Soluble 50% 1-methoxy-2-propanol 20% XIAMETER ™ PMX-200 Soluble Soluble Soluble 80% 1-methoxy-2-propanol
As shown above, depending on the specific blend and resin evaluated, resin solubility is observed in blends containing 20-50% of the hexamethyldisiloxane. This demonstrated the potential use of low VOC azeotropic blends as solvents with common resins used in coating compositions.