Vapor permeable, water resistive, air barrier polyester membrane having a polyacrylic coating with porous pressure sensitive adhesive added to the rear surface of the membrane

Abstract

An ultra violet stable polyester membrane with a polyacrylic coating on one side and a coated pressure sensitive adhesive coating on its other side capable of allowing water vapor to pass through it. The pressure sensitive adhesive is formed of a copolymer comprising a backbone of n-butyl acrylate, 2-ethylhexyl acrylate, and vinyl acetate which is mixed with at least one surfactant and emulsified to produce air bubbles which form pores when the copolymer is set with about 80% to about 90% of the pore sizes ranging from about 200 microns to about 300 microns and being uniformly distributed to form a flow path through the pressure sensitive adhesive.

Claims

1. A water resistive building membrane comprising: at least one permeable polyester plastic sheet having a front face, a polyacrylic coating coating the sheet's front face, a coating of permeable pressure sensitive acrylic; adhesive applied to an outer surface of the sheet opposite the sheet's front face, wherein the permeable pressure sensitive acrylic; adhesive comprises: at least 4000 entrained interconnected pores per square inch of adhesive, of which at least 80% of the pores have a size ranging from about 200 microns to about 300 microns, the pores being uniformly distributed and interconnected throughout the adhesive to form a water resistive water vapor flow path through the adhesive such that the adhesive has a vapor permeability of at least 40 Perms, and a copolymer with a backbone of n-butyl acrylate, 2-ethylhexyl acrylate, and vinyl acetate.

2. A water resistive building membrane as claimed in claim 1 wherein the pressure sensitive porous adhesive has a vapor permeability ranging from 40 to 70 Perms.

3. A water resistive building membrane as claimed in claim 1 wherein said pressure sensitive adhesive has a density ranging between about 0.65 to about 0.75.

4. A water resistive building membrane as claimed in claim 1 wherein said pressure sensitive adhesive has a pore density which ranges from 4000 per in.sup.2 to about 4600 per in.sup.2.

5. A water resistive building membrane as claimed in claim 1 wherein said pressure sensitive adhesive has a pore density of about 4400 per in.sup.2.

6. A water resistive building membrane as claimed in claim 1 wherein said pressure sensitive adhesive contains a flame-retardant material.

7. A water resistive building membrane as claimed in claim 6 wherein said flame retardant material is Antimony Oxide.

8. A water resistive building membrane as claimed in claim 6 wherein said flame retardant material is taken from a group consisting of halogenated fire suppressants, hydrated inorganic compounds selected from one of the following aluminum trihydrate, magnesium hydroxide, calcium borate and zinc borate, intumescent phosphate, ammonium polyphosphate, organic and inorganic phosphate compounds selected from one of the following ammonium sulfate, sulfamate compounds and free radical scavenger materials.

9. A water resistive building membrane as claimed in claim 6 wherein said flame retardant material is present in said pressure sensitive adhesive in a range of about 0.5% by weight to about 3% by weight.

10. A water resistive building membrane as claimed in claim 6 wherein said pressure sensitive adhesive contains a flame-retardant material in a range of about 2% by weight to about 3% by weight.

11. A water resistive building membrane comprising: a permeable polyester sheet with a polyacrylic coating, and a coating of permeable pressure sensitive adhesive applied to an outer surface of the sheet, wherein the permeable pressure sensitive acrylic adhesive comprises: at least 4000 entrained interconnected pores per square inch of adhesive, of which at least 80% of the pores have a size ranging from about 200 microns to about 300 microns, the pores having a rounded shape and being uniformly distributed and interconnected throughout the adhesive to form a water resistive water vapor flow path through the adhesive, and a copolymer with a backbone of n-butyl acrylate, 2-ethylhexyl acrylate, and vinyl acetate.

12. A water resistive building membrane as claimed in claim 11 wherein said pressure sensitive adhesive contains a flame-retardant material.

13. A water resistive building membrane as claimed in claim 11 wherein a release liner is placed on said pressure sensitive adhesive material.

14. A water resistive membrane as claimed in claim 11 wherein said pressure sensitive adhesive has a density ranging between about 0.65 and about 0.75 after aeration.

15. The membrane of claim 11 wherein the permeable pressure sensitive acrylic adhesive has a vapor permeability of at least 40 Perms.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) FIG. 1 is a perspective view of a roll of the inventive construction membrane;

(2) FIG. 2 is an enlarged partial broken apart cross sectional view of the construction membrane shown in FIG. 1 applied in a building construction environment;

(3) FIG. 3 is a side elevation view of a building construction using the present invention with components removed;

(4) FIG. 4 is a scanning electron microscopy photograph of the porous adhesive used with the construction membrane at 50× magnification; and

(5) FIG. 5 is a scanning electron microscopy photograph of the porous adhesive used with the construction membrane at 200× magnification.

DETAILED DESCRIPTION OF THE INVENTION

(6) The preferred embodiment and best mode of the invention is shown in FIGS. 1-5.

(7) A building construction membrane 10 in the form of a blank UV stable highly vapor permeable water resistive barrier, air barrier for open joint rain screen cladding system. UV stable means that it is applicable in all climates and sustains 180 days exposure to UV and climate prior to cladding installation. The inventive sheet 12 is constructed of a permeable polyester sheet with a polyacrylic coating 13 on its front face and has a layer of porous pressure sensitive adhesive 14 coated and set over a back portion of the sheet surface in the form of a strip or over the entire surface of the sheet. The composite sheet installs as a single layer black membrane and is particularly useful in connection with open joint rain screen cladding. It emits zero VOC's eliminating exposure to harmful and volatile chemicals. The surface of the adhesive is covered by a removable film cover or liner 15. When the release film liner 15 is removed, the back surface of membrane 12 with pressure sensitive adhesive 14 is mounted to a wall board or exterior sheathing or rigid insulation 16 which is secured to studs 17. As shown in FIG. 2, the outer face polyacrylic coating 13 is pressed against battens 18 which are secured to an open joint cladding 22. Air and vapor flow is shown by Arrows A and B, respectively.

(8) The membrane 10 is produced as a roll of sheet material 20, preferably 165 feet in length and with a width of 58-60 inches, preferably 59 inches. The membrane 10 is ultra violet (UV) stable water resistant and has a water vapor transmission greater than 40 Perms, preferably ranging from about 40 to about 70 Perms and acts as an air barrier. The produced membrane is inert and can be recycled for reuse.

(9) As shown in FIG. 3, an exterior sheeting or wall board 16 is mechanically fastened to studs 17 and the sheet 12 is adhesively secured to sheet 16. The sheet 12 may also be secured by the adhesive to rigid insulation or other wall substrates as gypsum sheathing. The open joint cladding 22 is fastened to the battens 18 by mechanical means.

(10) The pressure sensitive porous adhesive 14 is coated and cured on the back of the polyester/polyacrylic liner sheet 12 to fix the pores in place. The composite structure of the present invention has a high vapor permeability (40 to 50 Perms) and the adhesive breathes allowing vapor to escape while being water resistant.

(11) A Perm is a unit of water vapor transmission defined as 1 grain of water vapor per square foot per hour per inch of mercury pressure difference (1 inch mercury=0.49 psi). The metric unit of measure is ng/m2 s Pa. 1 perm=55 ng/m2 s Pa. Permeability is the time rate of water vapor transmission through unit area of a material of unit thickness induced by unit vapor pressure difference between two specific surfaces, under specified temperature and humidity conditions. Membranes with a higher Perm value greater than 20 reduce the risk of condensation and promote escape of moisture through the building envelope. Additionally, membranes with a high Perm value can help building materials dry-out during the construction phase.

(12) The copolymer portion of the pressure sensitive adhesive (PSA) has a backbone consisting of n-butyl acrylate, 2-ethylhexyl acrylate, and vinyl acetate. The structure of the backbone is shown in Table I below as follows:

(13) TABLE-US-00001 TABLE I (Structure of PSA Polymer Backbone)

(14) The adhesive fully bonds to almost any substitute for air tightness and ease of installation and requires no primer.

(15) The pressure sensitive adhesive (PSA) is an acrylic solution and bonds to the sheet 12. The polymeric portion of the PSA makes up at least 95% of the adhesive formulation and has a copolymer backbone of n-butyl acrylate (about 60% by weight), 2-ethylhexyl acrylate (about 32% by weight) and vinyl acetate (about 7% by weight) forming a copolymer solvent blend capable of accepting water. Proper foaming of the adhesive is critical to good micropore formation. The aeration process includes high sheer mixing to entrain air in the mixed liquid solution. Once the proper foam level is produced, the adhesive needs to be coated on the membrane sheet and the micropores formed.

(16) The coating method used with the present invention was a blade coater. This is a non-contact coating method and it does not crush or destroy the foam during coating. It should be noted that other coating methods such as Meyer rod, comma coating and pattern bar coating were attempted but found to be detrimental to suitable micropore formation. After coating, the adhesive must be heated to lock-in the micropore formation. The adhesive in the present invention was reformulated by adding surfactants and water to the copolymer to control bubble size, bubble density, viscosity, and stability of the copolymer. The peel value of the adhesive is reduced by the introduction of voids (air bubbles) and the addition of surfactant such as long chain alcohols create a stable inverse emulsion. The peel value of the presently formulated adhesive during testing using dynamic peel data from stainless steel (Peel Adhesion ASTM D-3330) was about 25 oz. in at 1 minute; 27.5 oz. in at 10 minutes and 36.5 oz. in at 24 hours.

(17) Microscopy of the modified adhesive surface was performed revealing a porous structure of the inventive adhesive having a bubble density (number of pores) ranging from about 4000 pores in 1.0 in.sup.2 to about 4600 pores in 1.0 in.sup.2, preferably about 4400 pores in 1.0 in.sup.2 with a majority of the pores, preferably about 80% to about 90% of the bubbles/pores having a size ranging from about 200 microns to about 300 microns. See FIGS. 4 and 5. The pores formed are generally round and oval in shape and form a vapor pathway through the adhesive layer. The majority of the pores 100 formed by the entrained air bubbles appear to be distributed evenly across the surface penetrating through the adhesive layer when the polymer mixture is heat treated to set or cure the pores in the adhesive. The pore distribution is shown in FIG. 5. Preferably, the density of the foamed adhesive should fall between about 0.65 and about 0.75 after aeration.

(18) The reformatted PSA was manufactured as follows:

(19) The adhesive copolymer as shown in Table I ranged from about 45% by weight to about 50% by weight, preferably about 48% to about 49% by weight. The copolymer was mixed with a first solvent-free, surfactant-based wetting agent, preferably ranging from about 4% by weight to about 6% by weight, and most preferably about 5% by weight to provide emulsification and bubble size; and a second surfactant such as a foaming agent ranging from about 1.5% by weight to about 2.0% by weight, and preferably about 1.7% by weight to provide foam formation. A polymeric based water thickener was added to the mixture in a range from about 0.2% by weight to about 0.4% by weight, preferably about 0.30% by weight. The composition was added to water ranging from about 40% by weight to about 50% by weight, preferably about 43% by weight to about 45% by weight and mixed in a high speed dispersion mixer at 500 rpm to form uniform bubbles in the mixture and fed into a coater feeder as previously described. The foamed adhesive was coated onto a porous polyacrylic coated polyester liner sheet and heat cured to form an adhesive laminate with pores in place. The resultant foamed adhesive had average MVTR (g/m.sup.2 day) of about 500 with a Peel adh @1800 (measured stability) ranging from about 65 to IS, preferably about 40.

(20) The pressure sensitive porous adhesive construction membrane is preferably made by adding a coating of adhesive as a strip on the liner sheet with the composition of the adhesive noted above. If desired, as a building covering membrane, the entire rear surface of the sheet can be covered with the porous adhesive.

(21) In a modified version, a flame retardant material Antimony Oxide was added to the adhesive mixture at about 2% by weight to about 3% by weight. Other flame retardant materials suitable for use with the adhesive may include halogenated fire suppressants, hydrated inorganic compounds such as aluminum trihydrate, magnesium hydroxide, calcium borate and zinc borate, intumescent phosphate, ammonium polyphosphate, organic and inorganic phosphate compounds such as ammonium sulfate, sulfamate compounds and free radical scavenger materials such as antimony trioxide.

(22) The principles, preferred embodiments and modes of operation of the present invention have been described in the foregoing specification. However, the invention should not be construed as limited to the particular embodiments which have been described above. Instead, the embodiments described here should be regarded as illustrative rather than restrictive. Variations and changes may be made by others without departing from the scope of the present inventions defined by the following claims.