CA2070489A1 - Gypsum board coating - Google Patents
Gypsum board coatingInfo
- Publication number
- CA2070489A1 CA2070489A1 CA 2070489 CA2070489A CA2070489A1 CA 2070489 A1 CA2070489 A1 CA 2070489A1 CA 2070489 CA2070489 CA 2070489 CA 2070489 A CA2070489 A CA 2070489A CA 2070489 A1 CA2070489 A1 CA 2070489A1
- Authority
- CA
- Canada
- Prior art keywords
- wax
- gypsum board
- barrier layer
- layer
- moisture vapour
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
- 239000010440 gypsum Substances 0.000 title claims abstract description 72
- 229910052602 gypsum Inorganic materials 0.000 title claims abstract description 72
- 239000011248 coating agent Substances 0.000 title claims description 31
- 238000000576 coating method Methods 0.000 title claims description 31
- 239000001993 wax Substances 0.000 claims abstract description 57
- 230000004888 barrier function Effects 0.000 claims abstract description 27
- 239000012188 paraffin wax Substances 0.000 claims abstract description 25
- 238000007766 curtain coating Methods 0.000 claims abstract description 22
- 239000012943 hotmelt Substances 0.000 claims abstract description 16
- 239000004200 microcrystalline wax Substances 0.000 claims abstract description 14
- 235000019808 microcrystalline wax Nutrition 0.000 claims abstract description 14
- 239000000463 material Substances 0.000 claims abstract description 13
- -1 polyethylene Polymers 0.000 claims abstract description 12
- 239000004698 Polyethylene Substances 0.000 claims abstract description 11
- 229920000573 polyethylene Polymers 0.000 claims abstract description 11
- 239000005038 ethylene vinyl acetate Substances 0.000 claims abstract description 10
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 claims abstract description 10
- 238000005507 spraying Methods 0.000 claims abstract description 7
- 239000000155 melt Substances 0.000 claims abstract description 3
- 238000000034 method Methods 0.000 claims description 40
- 238000002844 melting Methods 0.000 claims description 18
- 230000008018 melting Effects 0.000 claims description 18
- 239000000203 mixture Substances 0.000 claims description 16
- 229940114937 microcrystalline wax Drugs 0.000 claims description 9
- 229920005989 resin Polymers 0.000 claims description 9
- 239000011347 resin Substances 0.000 claims description 9
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 6
- 239000003963 antioxidant agent Substances 0.000 claims description 6
- 229920001400 block copolymer Polymers 0.000 claims description 6
- 230000003078 antioxidant effect Effects 0.000 claims description 5
- 229920001971 elastomer Polymers 0.000 claims description 5
- 239000005060 rubber Substances 0.000 claims description 5
- ADCOVFLJGNWWNZ-UHFFFAOYSA-N antimony trioxide Chemical compound O=[Sb]O[Sb]=O ADCOVFLJGNWWNZ-UHFFFAOYSA-N 0.000 claims description 4
- 239000003063 flame retardant Substances 0.000 claims description 3
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 claims description 2
- DQXBYHZEEUGOBF-UHFFFAOYSA-N but-3-enoic acid;ethene Chemical compound C=C.OC(=O)CC=C DQXBYHZEEUGOBF-UHFFFAOYSA-N 0.000 claims description 2
- 239000003365 glass fiber Substances 0.000 claims description 2
- 229940076134 benzene Drugs 0.000 claims 1
- 230000015572 biosynthetic process Effects 0.000 abstract description 4
- 230000001680 brushing effect Effects 0.000 abstract description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 16
- 239000010410 layer Substances 0.000 description 11
- 235000019809 paraffin wax Nutrition 0.000 description 11
- 235000019271 petrolatum Nutrition 0.000 description 11
- 238000002203 pretreatment Methods 0.000 description 7
- 229920001577 copolymer Polymers 0.000 description 6
- 238000007757 hot melt coating Methods 0.000 description 6
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- 239000008199 coating composition Substances 0.000 description 4
- 230000035515 penetration Effects 0.000 description 4
- 239000000758 substrate Substances 0.000 description 4
- 238000011282 treatment Methods 0.000 description 4
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 3
- 239000010426 asphalt Substances 0.000 description 3
- 239000011888 foil Substances 0.000 description 3
- 239000007921 spray Substances 0.000 description 3
- 235000010919 Copernicia prunifera Nutrition 0.000 description 2
- 244000180278 Copernicia prunifera Species 0.000 description 2
- 239000005977 Ethylene Substances 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 239000005030 aluminium foil Substances 0.000 description 2
- 238000010276 construction Methods 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 239000002985 plastic film Substances 0.000 description 2
- 239000013074 reference sample Substances 0.000 description 2
- MRAKLTZPBIBWFH-ARJAWSKDSA-N (z)-2-ethenylbut-2-enedioic acid Chemical compound OC(=O)\C=C(\C=C)C(O)=O MRAKLTZPBIBWFH-ARJAWSKDSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- JLBJTVDPSNHSKJ-UHFFFAOYSA-N 4-Methylstyrene Chemical compound CC1=CC=C(C=C)C=C1 JLBJTVDPSNHSKJ-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 229920006272 aromatic hydrocarbon resin Polymers 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 239000004566 building material Substances 0.000 description 1
- 239000013068 control sample Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- BXOUVIIITJXIKB-UHFFFAOYSA-N ethene;styrene Chemical compound C=C.C=CC1=CC=CC=C1 BXOUVIIITJXIKB-UHFFFAOYSA-N 0.000 description 1
- 229920006242 ethylene acrylic acid copolymer Polymers 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- FTQWRYSLUYAIRQ-UHFFFAOYSA-N n-[(octadecanoylamino)methyl]octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(=O)NCNC(=O)CCCCCCCCCCCCCCCCC FTQWRYSLUYAIRQ-UHFFFAOYSA-N 0.000 description 1
- 235000013873 oxidized polyethylene wax Nutrition 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 229920006255 plastic film Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 150000003097 polyterpenes Chemical class 0.000 description 1
- 238000005086 pumping Methods 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 229920002725 thermoplastic elastomer Polymers 0.000 description 1
- 238000009834 vaporization Methods 0.000 description 1
- 230000008016 vaporization Effects 0.000 description 1
- 238000004078 waterproofing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B41/00—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
- C04B41/009—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone characterised by the material treated
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B41/00—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
- C04B41/45—Coating or impregnating, e.g. injection in masonry, partial coating of green or fired ceramics, organic coating compositions for adhering together two concrete elements
- C04B41/4505—Coating or impregnating, e.g. injection in masonry, partial coating of green or fired ceramics, organic coating compositions for adhering together two concrete elements characterised by the method of application
- C04B41/4523—Coating or impregnating, e.g. injection in masonry, partial coating of green or fired ceramics, organic coating compositions for adhering together two concrete elements characterised by the method of application applied from the molten state ; Thermal spraying, e.g. plasma spraying
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B41/00—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
- C04B41/45—Coating or impregnating, e.g. injection in masonry, partial coating of green or fired ceramics, organic coating compositions for adhering together two concrete elements
- C04B41/46—Coating or impregnating, e.g. injection in masonry, partial coating of green or fired ceramics, organic coating compositions for adhering together two concrete elements with organic materials
- C04B41/47—Oils, fats or waxes natural resins
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B41/00—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
- C04B41/60—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone of only artificial stone
- C04B41/61—Coating or impregnation
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B41/00—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
- C04B41/60—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone of only artificial stone
- C04B41/61—Coating or impregnation
- C04B41/62—Coating or impregnation with organic materials
-
- E—FIXED CONSTRUCTIONS
- E04—BUILDING
- E04C—STRUCTURAL ELEMENTS; BUILDING MATERIALS
- E04C2/00—Building elements of relatively thin form for the construction of parts of buildings, e.g. sheet materials, slabs, or panels
- E04C2/02—Building elements of relatively thin form for the construction of parts of buildings, e.g. sheet materials, slabs, or panels characterised by specified materials
- E04C2/04—Building elements of relatively thin form for the construction of parts of buildings, e.g. sheet materials, slabs, or panels characterised by specified materials of concrete or other stone-like material; of asbestos cement; of cement and other mineral fibres
- E04C2/043—Building elements of relatively thin form for the construction of parts of buildings, e.g. sheet materials, slabs, or panels characterised by specified materials of concrete or other stone-like material; of asbestos cement; of cement and other mineral fibres of plaster
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2111/00—Mortars, concrete or artificial stone or mixtures to prepare them, characterised by specific function, property or use
- C04B2111/00474—Uses not provided for elsewhere in C04B2111/00
- C04B2111/00612—Uses not provided for elsewhere in C04B2111/00 as one or more layers of a layered structure
- C04B2111/0062—Gypsum-paper board like materials
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Ceramic Engineering (AREA)
- Structural Engineering (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Architecture (AREA)
- Physics & Mathematics (AREA)
- Plasma & Fusion (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Civil Engineering (AREA)
- Laminated Bodies (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
Abstract
ABSTRACT
A gypsum board having an integrated moisture vapour barrier layer of an improved moisture vapour impermeability is disclosed. The layer is applied to the surface of the board by curtain coating a hot melt of a material comprising a natural or synthetic wax, such as a paraffin or polyethylene wax and, for example, an ethylene-vinyl acetate copolymer or a microcrystalline wax, and permitting the melt to cool. To improve the integrity of the moisture vapour barrier layer by reducing the formation of pinholes and blisters during the curtain coating, a layer of a paraffin or microcrystalline wax may be applied to the surface of the board, for example by brushing or spraying, prior to curtain coating.
A gypsum board having an integrated moisture vapour barrier layer of an improved moisture vapour impermeability is disclosed. The layer is applied to the surface of the board by curtain coating a hot melt of a material comprising a natural or synthetic wax, such as a paraffin or polyethylene wax and, for example, an ethylene-vinyl acetate copolymer or a microcrystalline wax, and permitting the melt to cool. To improve the integrity of the moisture vapour barrier layer by reducing the formation of pinholes and blisters during the curtain coating, a layer of a paraffin or microcrystalline wax may be applied to the surface of the board, for example by brushing or spraying, prior to curtain coating.
Description
~7~ 9 2796~-2 GYPSUM BOARD COATING
This lnvention relates to gypsum board provided with an integrated molsture vapour barrie:r and to a method of preparing such gypsum board. The invention also relates to a method of treating gypsum board prior to cuxtain coating to improve the moisture vapour impermeability of the coating.
Panels of gypsum board are a well known building material used mostly to form walls and ceilings of buildings and also, to some extent, as an exterior material. While gypsum boards provide excellent fire resistance, they also have a dis-advantage of being susceptible to moisture, which easily pene-- trates into and through the boards. When put in contact with liquid water, gypsum board absorbs in a short time a considerable amount of water. This usually damages the board in that it causes ; deformation, decreases mechanical strength and may even destroy the structural integrity of the board.
Numerous attempts to enhance the water resistance of ~- gypsum boards are known from the prior art. The most common practice is the incorporation of water-dispersible hydrophobic materials, such as paraffin wax or asphalt, into gypsum slurry prior to setting (see, for example, U.S. 2,604,411). Another approach is a surface post-treatment of gypsum boards, by applying a water impermeable or repellant coating to the surface (see, for example, U.S. 4,350,736, U.S. 3,839,141 and U.S. 3,850,680).
The moisture resistance of a surface coating may be seriously impaired if pinholes are formed in the process of coating. This happens, for example, when the surface of a gypsum ~ 1 .
~ . ~
~. .
. . ' ' .
:
~7~
2796~-2 board is being covered with a hot material. Such a process usual-ly results in blistering o~ the coating and in disr~lpting of the integrity of th~ produced coating.
The effect of blistering was noted, for example, in U.S.
4,879,173, where hot asphalt was applied to gypsum boards used in roof construc-tion. In this process gypsum boards faced on both sides with a glass filament mat were used. Blister formation was attributed to the vaporization of water contained in the gypsum itself, caused by contact with the hot asphalt ~400-450F). Pre-treatment of the gypsum board with little amounts of a reinforcingresin binder prevented the formation of blisters without affecting the drying characteristics of the board, i.e. without providing a barrier to the passage o water vapour.
The known waterproofing treatments, even though impart-ing resistance to the entry of liquid water, usually do not pro-vide an efficient moisture vapour barrier. The inclusion of such a barrier, in particular in an exterior wall or a ceiling structure of a building is a standard practice in the fabrication of buildings and can be accomplished by various methods, such as extending large sheets of plastic film, for example polyethylene, - throughout the vapour protected surface.
The prior art of producing gypsum boards having moisture vapour barrier properties, for use in constructions, is limited to laminating aluminum foil to the paper backing of the gypsum board (see, for example, CA 1,091,566). The aluminum foil must be glued manually to each sheet of drywall, which makes the process both time consuming and expensive.
. ' ' ~7~3~3 2796~-2 According to one aspect, the invention provides a method for coating a gypsum board to provide a gypsum board having a moisture vapour barrier layer on a surface thereof, which method comprises applying to the surface by curtain coating a hot melt of a material that will cool to form a moisture vapour barrier layer and permitting the melt to cool to form the required moisture vapour barrier layer.
According to another aspect, the invention provides a gypsum board having a moisture vapour barrier layer applied to a surface of the board by curtain coating a hot melt of a material that form -the moisture vapour barrier layer when permitted to ` cool.
Since the application of a vapour barriers by curtain coating is carried out mechanically, labour requirements and costs are reduced and the overall speed of the production line may be increased. The curtain coating material is also less expensive, leading to further reduction in costs.
In ~he curtain coating process, the coating composition is delivered in a falling sheet or curtain onto the substrate, which is moved through the curtain at a controlled rate. The coating composition must be sufficiently fluid to fall freely and sufficiently cohesive to form a continuous film on the substrate.
In one embodiment of the invention, the coating composition is first melted and heated in a tank to the required temperature.
The composition is then pumped from the tank to a reservoir which has a wide, narrow slit opening in its bottom. The slit allows a : ~:
wide, thin flow of molten coating, referred to as a curtain, to :~ 3 ~. . . ~ :......... ' ~ . ' : - . , : . ' , ' . :,, . ' ' ' fall upon the substrate as it passes underneath the reservoir.
The thickness of the resulting coating can be controlled by vary-ing the slit opening, the rate of pumping of the molten composi-tion and/or the speed at which the substrate is passed under the slit.
In the conventional process of producing gypsum boards, the wet gypsum board is placed in an oven to remove excess water.
According to the invention, the gypsum board may be curtain coated directly upon leaving the oven or, alternatively, after cooling or being cooled to required temperature, for example the ambient temperature. If coating takes place immediately after the board leaves the oven, the melting point of the hot melt coating material must be higher than the temperature of the gypsum board - as it leaves the oven. In general, application temperatures of the hot melt may range from about 180 to about 350F. Application temperatures from about 250 to about 300F are preferred.
The thickness of the coating may be adjusted as re-quired. A thickness of from about one-half to about ten thousandths of an inch has been found satisfactory for most applications, a thickness of from about two to about four thousandths of an inch being preferred. The board may be coated - in one or several passes through a curtain coating machine. A
single or double pass is preferred. Depending on the intended application of the board, the coating may be applied to one or to both faces of the gypsum board.
The preferred gypsum board to receive the coating according to the invention is of the standard type, having a core :
~ 4 ... , ~
~ ~ .
.
.,: ~ ~ :
:` ~
This lnvention relates to gypsum board provided with an integrated molsture vapour barrie:r and to a method of preparing such gypsum board. The invention also relates to a method of treating gypsum board prior to cuxtain coating to improve the moisture vapour impermeability of the coating.
Panels of gypsum board are a well known building material used mostly to form walls and ceilings of buildings and also, to some extent, as an exterior material. While gypsum boards provide excellent fire resistance, they also have a dis-advantage of being susceptible to moisture, which easily pene-- trates into and through the boards. When put in contact with liquid water, gypsum board absorbs in a short time a considerable amount of water. This usually damages the board in that it causes ; deformation, decreases mechanical strength and may even destroy the structural integrity of the board.
Numerous attempts to enhance the water resistance of ~- gypsum boards are known from the prior art. The most common practice is the incorporation of water-dispersible hydrophobic materials, such as paraffin wax or asphalt, into gypsum slurry prior to setting (see, for example, U.S. 2,604,411). Another approach is a surface post-treatment of gypsum boards, by applying a water impermeable or repellant coating to the surface (see, for example, U.S. 4,350,736, U.S. 3,839,141 and U.S. 3,850,680).
The moisture resistance of a surface coating may be seriously impaired if pinholes are formed in the process of coating. This happens, for example, when the surface of a gypsum ~ 1 .
~ . ~
~. .
. . ' ' .
:
~7~
2796~-2 board is being covered with a hot material. Such a process usual-ly results in blistering o~ the coating and in disr~lpting of the integrity of th~ produced coating.
The effect of blistering was noted, for example, in U.S.
4,879,173, where hot asphalt was applied to gypsum boards used in roof construc-tion. In this process gypsum boards faced on both sides with a glass filament mat were used. Blister formation was attributed to the vaporization of water contained in the gypsum itself, caused by contact with the hot asphalt ~400-450F). Pre-treatment of the gypsum board with little amounts of a reinforcingresin binder prevented the formation of blisters without affecting the drying characteristics of the board, i.e. without providing a barrier to the passage o water vapour.
The known waterproofing treatments, even though impart-ing resistance to the entry of liquid water, usually do not pro-vide an efficient moisture vapour barrier. The inclusion of such a barrier, in particular in an exterior wall or a ceiling structure of a building is a standard practice in the fabrication of buildings and can be accomplished by various methods, such as extending large sheets of plastic film, for example polyethylene, - throughout the vapour protected surface.
The prior art of producing gypsum boards having moisture vapour barrier properties, for use in constructions, is limited to laminating aluminum foil to the paper backing of the gypsum board (see, for example, CA 1,091,566). The aluminum foil must be glued manually to each sheet of drywall, which makes the process both time consuming and expensive.
. ' ' ~7~3~3 2796~-2 According to one aspect, the invention provides a method for coating a gypsum board to provide a gypsum board having a moisture vapour barrier layer on a surface thereof, which method comprises applying to the surface by curtain coating a hot melt of a material that will cool to form a moisture vapour barrier layer and permitting the melt to cool to form the required moisture vapour barrier layer.
According to another aspect, the invention provides a gypsum board having a moisture vapour barrier layer applied to a surface of the board by curtain coating a hot melt of a material that form -the moisture vapour barrier layer when permitted to ` cool.
Since the application of a vapour barriers by curtain coating is carried out mechanically, labour requirements and costs are reduced and the overall speed of the production line may be increased. The curtain coating material is also less expensive, leading to further reduction in costs.
In ~he curtain coating process, the coating composition is delivered in a falling sheet or curtain onto the substrate, which is moved through the curtain at a controlled rate. The coating composition must be sufficiently fluid to fall freely and sufficiently cohesive to form a continuous film on the substrate.
In one embodiment of the invention, the coating composition is first melted and heated in a tank to the required temperature.
The composition is then pumped from the tank to a reservoir which has a wide, narrow slit opening in its bottom. The slit allows a : ~:
wide, thin flow of molten coating, referred to as a curtain, to :~ 3 ~. . . ~ :......... ' ~ . ' : - . , : . ' , ' . :,, . ' ' ' fall upon the substrate as it passes underneath the reservoir.
The thickness of the resulting coating can be controlled by vary-ing the slit opening, the rate of pumping of the molten composi-tion and/or the speed at which the substrate is passed under the slit.
In the conventional process of producing gypsum boards, the wet gypsum board is placed in an oven to remove excess water.
According to the invention, the gypsum board may be curtain coated directly upon leaving the oven or, alternatively, after cooling or being cooled to required temperature, for example the ambient temperature. If coating takes place immediately after the board leaves the oven, the melting point of the hot melt coating material must be higher than the temperature of the gypsum board - as it leaves the oven. In general, application temperatures of the hot melt may range from about 180 to about 350F. Application temperatures from about 250 to about 300F are preferred.
The thickness of the coating may be adjusted as re-quired. A thickness of from about one-half to about ten thousandths of an inch has been found satisfactory for most applications, a thickness of from about two to about four thousandths of an inch being preferred. The board may be coated - in one or several passes through a curtain coating machine. A
single or double pass is preferred. Depending on the intended application of the board, the coating may be applied to one or to both faces of the gypsum board.
The preferred gypsum board to receive the coating according to the invention is of the standard type, having a core :
~ 4 ... , ~
~ ~ .
.
.,: ~ ~ :
:` ~
2 ~ r~ 8 ~l 279~4-2 of set yypsum sandwiched between two sheets of facing paper.
However, other types of gypsum boards, for example those haviny facing sheets of glass fibers, as described in U.S. patent 4,879,173, or even those having th~e core waterproofed by admixing water-resistant additives, such as wax emulsions, may also be used.
A preferred hot melt applied by curtain coating com-prises a paraffin wax admixed with one or more of the following:
ethylene-vinyl acetate copolymer, tackifying resins, styrene-rubber block copolymers, an N,N'-ethylene bis-amide and micro-crystalline wax.
Synthetic or natural waxes other than a paxaffin wax may be used as components in the curtain coating blend. Examples of ; synthetic waxes may be polyethylene waxes, oxidized polyethylene waxes, chlorinated paraffin waxes and Fisher-Tropsch waxes.
Examples of natural waxes may be carnauba and candellila waxes.
;~ Similarly, other polymers and copolymers, such as ethylene-maleic acid anhydride copolymer, ethylene-acrylic acid copolymer, ethylene-acrylic ester copolymers, ethylene-alkyl acrylic acid and ester copolymers, as well as ionically crosslinked variations thereof can also be used in combination with or in place of the ethylene-vinyl acetate and styrene-rubber block copolymers.
Ethylene-vinyl acetate copolymer having acetate content of from about 5% to about 50%, preferably from about 18~ to about 28%, with softening points up to about 400F may be used.
Tackifying resins suitable for the practice of the invention include C5 aliphatic and Cg aromatic hydrocarbon resins .
, -,: :
27g6~-2 and copolymers, resin acids and derivati~es thereof, ~tyrenic and polyterpene resins and copolymers and phenolic resins, with softening points up to about 140C. The choice of resin is made according to softening point, colour and compatibility require-ment, well known to those skilled in the art.
Styrene-rubber block copolymers are thermoplastic rubbers which are block copolymers composed of styrene or methyl styrene in combination with one or more of ethylene, butylene, isoprene, and isobutylene. The styrene content may range from about 10 to about 50%.
N,N'-Ethylene bis-amides are di-amide waxes, containing either bis-stearami~e or bis-oleamide with melting points of 110-120C and 130 150C, respectively.
In general, the coating composition may comprise 54-90 paraffin wax, 0-20% microcrystalline wax, 0-25% ethylene-vinyl acetate copolymer, 0-10% tackifying resin, 0-10% low molecular weight polyethylene wax, and 0-6% styrene-rubber block copolymer.
A composition comprising from about 65~ to about 90% paraffin wax, from about 5% to about 20% ethylene-vinyl acetate copolymer, from about 5% to about 10% tackifying resin and from 0% to about 5% low molecular weight polyethylene wax is preferred.
The hot melt used for curtain coating may contain further additives, such as antioxidants and/or flame retardants.
1,3,5-Trimethyl-~,4,6-tris-(3,5-di-tert-4-hydroxybenzyl)benzene is preferred as antioxidant. The preferred flame retardant composi-tion is obtained by combining 100 parts by weight of the hot melt -,. ~ .
2 ~
~ 796~-2 coating with 5 parts by welght of chlorinated paraffin and 2.5 parts by weight of antimony trioxide.
The gypsum board coated according to the invention is characterized by an improved moisture vapour impermeability.
However, as discussed earlier in connection with U.S. 4,879,173, the application of a hot melt coating to the surface of a gypsum board may result in formation of pinholes and blisters in the coating as it solidifies. This, in turn, may impair the moisture vapour properties of the coating. It is believed that the pin-holes and blisters form as a result of water present in the paperfacing and/or the core of the gypsum board, which water vaporizes upon contact with hot melt coating, which may be applied at temperatures as high as 350F. It has now been found that this adverse effect can be substantially reduced by covering the surface of the gypsum board with a layer of a paraffin or micro-crystalline wax, or a mixture thereof, prior to curtain coating.
~ It is believed that this pre-treatment of the gypsum board serves - the purpose of both absorbing heat from the molten hot melt and providing an additional barrier to the vaporized water, thus preserving the integrity of the subsequently applied hot melt coating as the hot melt solidifies.
Waxes suitable for the pre-treatment are those capable of forming a surface layer at the facing of the gypsum board.
These include paraffin and microcrystalline waxes, polyethylene waxes, Fischer-Tropsch waxes, and natural waxes, such as carnauba and candellila waxes. For the purpose of pre-treatment, the hot -~ melt curtain coating material may also be applied.
`'. , ~" 7 , ' ~.` ' . `' '' . :: ' , ~`' ` ~ . , .
Penetration of wax into the paper facing is not desir-able, in that it increases the amount of the material used without significantly increasing the beneficial effects of the treatment.
Factors which determine the degree of penetration of the wax into the paper facing include the method of application, the melting point of the wax and the temperature of the gypsum board, as dis-cussed below.
For the pre-treatment, various methods of applying the molten wax to the surface of the gypsum board, such as brushing or spraying, may be used. Of these, spraying molten wax is pre-ferred. It was found that spraying allows control over the degree of penetration of wax into the paper facing, by adjusting -the wax temperature, spraying intensity, and spraying distance.
Paraffin waxes with melting points in a range of from about 120 to about 165F and microcrystalline waxes with melting points of from about 150 to about 1930F have been found to be suitable for application at room temperature to gypsum boards.
; The applied wax blend may consist entirely of paraffin or micro-crystalline wax, or it may be a mixture of the two.
Pr -treatment of the gypsum board may take place immedi-ately after the board leaves the drying oven. In this case, the melting point of the wax or wax blend should be preferably greater than the temperature of the gypsum board. If the melting point of the wax is lower than the temperature o~ the gypsum board to be coated, excessive penetration of wax into the paper facing will occur. Consequently, proper selection of the wax or wax blend '~' ' : ' .
- ' .
2~7~3s~
with which to spray the gypsum board is important. If the temperature of the gypsum board is 1400F, then paraffin waxes with melting polnts in the range of from about 140 to about 165F or microcrystalline waxes with melting points in the range of from about 150 to about 193F may be used alone or in combination wi~h each other. Paraffin waxes with melting points lower than 140F
may be used in combination with waxes of higher melting points to produce a blend of sufficiently high melting point.
The thickness of the wax pre-treatment layer may be varied as required, but is normally in the range of from about one-half to about 10 thousandths of an inch. A thickness of from ; about 2 to about 4 thousandths of an inch is preferred. Depending on the intended application of the board, the wax layer may be applied to one or to both sides of the gypsum board. Curtain coating may take place immediately after applying the wax coating,:
or after allowing the wax coating to cool to ambient temperature.
When the surface of the board was pre-treated according to the invention, it could be observed that in some cases bubbles were absent from the subsequently applied coating, whereas in other cases bubbles trapped in the coating were noted, but the coating surface integrity was not affected. Thus, the wax layer effectively absorbs heat from the hot melt in the former cases, whereas in the latter cases it impedes expulsion of water vapour through the coating surface.
The invention will be further described by way of a ~ preferred embodiment and non-limiting examples.
.; 9 , .
- . ' i .
.'.~ ` ~
` , ' ' ' '~, . ;, .' '' '~ , `2 ~
2796~-2 ~L~ 1 An 111- X 11" piece of gypsum board was warmed in an oven to 140F, then removed from the oven and i.mmediately passed twice through a curtain coater. From the curtain coater was applied a hot melt coating having temperature of 300F and comprising a blend of 17.5% ethylene-vinyl acetate copolymer and 82.5% of paraffin having melting point o~ 140F. The coating thickness of each pass was 2 thousandths of an inch for a final thickness of ~ thousandths of an inch.
10 EXAMI?LE 2 Gypsum board was cut into 11" x 11" pieces and warmed in an oven to 140F. The boards were removed from the oven one at a time and immediately sprayed on one side with a paraffin wax having melting point of 160F, using a hand held spray gun driven by compressed nitrogen gas. The final coating thickness of the wax layer was 4 thousandths of an inch. The wax coated board was immediately curtain coated with a blend of 17.5~ ethylene-vinyl acetate copolymer and 82.5% of paraffin having melting point of 140F, at an application temperature of 300F. The thickness of the hot melt coating was 2 thousandths of an inch.
EXAMPL~ 3 A 11" x 11" piece of gypsum board having room tempera-ture was sprayed on one side with a paraffin having melting poin~
of 120F using a hand held spray gun, as in Example 2. The thick-ness of this coating was 4 thousandths of an inch. Curtain coating was carried out as in Example 1. In this case, some .
.
: . .
~; ' . .
2 ~
bubbles were no~ed in the coating, but they were retained in the coating and did not disrupt the surface integrity.
The coated gypsum boards from Examples 1, 2 and 3 were tested in a controlled environment cabinet with a relative humidity of 92~ at a temperature of 100F. To prevent the entry of water through the untreated surfaces of the board the uncoated sides of the gypsum boards were covered with a double layer of a polyethylene plastic sheet covered with a sheet of aluminium foil.
A control sample consisted of an 11" x 11" piece of gypsum board completely covered with polyethylene plastic and aluminium foil.
A reference sample was identical with samples of examples 1, 2 and 3 except that it was not pretreated with wax nor curtain coated.
The edges of the gypsum boards were sealed by dipping in a 60/40 mixture of microcrystalline wax/paraffin wax. After the samples were covered and sealed, the surface area exposed to moisture vapour was in each case nine square inches. The samples were weighed, placed in the controlled environment cabinet for twenty-four hours and weighed again. The difference between the weight after the exposure in the cabinet and the original weight constituted the water uptake. The values repor~ed in the follow-ing table are averages of at least two determinations.
~ .
.; ., . ~ . :
. ' ' '~ , ~ ' ~
:; :
~ , ~7~89 27g6~-2 5~MPL~ ~T~ ~PTAX~ (GR~M5 Control o Reference 7.3 Example 1 0.42 Example 2 0.06 Example 3 0.12 The ~ater uptake of the control demonstrates that the wrapping with polyethylene plastic and aluminum foil was effective in preventing passage of moisture. Consequently, any water uptake will have occurred through untreated surfaces, in the reference sample, or through surfaces treated in accordance with the inven-tion, in Examples 1, 2 and 3.
The results clearly demonstrate the moisture vapour ~; barrier properties of the curtain coated gypsum board (Example 1) compared with the uncoated board ~Reference), as measured by the amount of moisture penetrating into the board in the form of vapour. Examples 2 and 3 also show the effectiveness of the wax ~ pre-treatment in improving the moisture vapour barrier properties : of the curtain coating.
~, :
,'~ ' .,
However, other types of gypsum boards, for example those haviny facing sheets of glass fibers, as described in U.S. patent 4,879,173, or even those having th~e core waterproofed by admixing water-resistant additives, such as wax emulsions, may also be used.
A preferred hot melt applied by curtain coating com-prises a paraffin wax admixed with one or more of the following:
ethylene-vinyl acetate copolymer, tackifying resins, styrene-rubber block copolymers, an N,N'-ethylene bis-amide and micro-crystalline wax.
Synthetic or natural waxes other than a paxaffin wax may be used as components in the curtain coating blend. Examples of ; synthetic waxes may be polyethylene waxes, oxidized polyethylene waxes, chlorinated paraffin waxes and Fisher-Tropsch waxes.
Examples of natural waxes may be carnauba and candellila waxes.
;~ Similarly, other polymers and copolymers, such as ethylene-maleic acid anhydride copolymer, ethylene-acrylic acid copolymer, ethylene-acrylic ester copolymers, ethylene-alkyl acrylic acid and ester copolymers, as well as ionically crosslinked variations thereof can also be used in combination with or in place of the ethylene-vinyl acetate and styrene-rubber block copolymers.
Ethylene-vinyl acetate copolymer having acetate content of from about 5% to about 50%, preferably from about 18~ to about 28%, with softening points up to about 400F may be used.
Tackifying resins suitable for the practice of the invention include C5 aliphatic and Cg aromatic hydrocarbon resins .
, -,: :
27g6~-2 and copolymers, resin acids and derivati~es thereof, ~tyrenic and polyterpene resins and copolymers and phenolic resins, with softening points up to about 140C. The choice of resin is made according to softening point, colour and compatibility require-ment, well known to those skilled in the art.
Styrene-rubber block copolymers are thermoplastic rubbers which are block copolymers composed of styrene or methyl styrene in combination with one or more of ethylene, butylene, isoprene, and isobutylene. The styrene content may range from about 10 to about 50%.
N,N'-Ethylene bis-amides are di-amide waxes, containing either bis-stearami~e or bis-oleamide with melting points of 110-120C and 130 150C, respectively.
In general, the coating composition may comprise 54-90 paraffin wax, 0-20% microcrystalline wax, 0-25% ethylene-vinyl acetate copolymer, 0-10% tackifying resin, 0-10% low molecular weight polyethylene wax, and 0-6% styrene-rubber block copolymer.
A composition comprising from about 65~ to about 90% paraffin wax, from about 5% to about 20% ethylene-vinyl acetate copolymer, from about 5% to about 10% tackifying resin and from 0% to about 5% low molecular weight polyethylene wax is preferred.
The hot melt used for curtain coating may contain further additives, such as antioxidants and/or flame retardants.
1,3,5-Trimethyl-~,4,6-tris-(3,5-di-tert-4-hydroxybenzyl)benzene is preferred as antioxidant. The preferred flame retardant composi-tion is obtained by combining 100 parts by weight of the hot melt -,. ~ .
2 ~
~ 796~-2 coating with 5 parts by welght of chlorinated paraffin and 2.5 parts by weight of antimony trioxide.
The gypsum board coated according to the invention is characterized by an improved moisture vapour impermeability.
However, as discussed earlier in connection with U.S. 4,879,173, the application of a hot melt coating to the surface of a gypsum board may result in formation of pinholes and blisters in the coating as it solidifies. This, in turn, may impair the moisture vapour properties of the coating. It is believed that the pin-holes and blisters form as a result of water present in the paperfacing and/or the core of the gypsum board, which water vaporizes upon contact with hot melt coating, which may be applied at temperatures as high as 350F. It has now been found that this adverse effect can be substantially reduced by covering the surface of the gypsum board with a layer of a paraffin or micro-crystalline wax, or a mixture thereof, prior to curtain coating.
~ It is believed that this pre-treatment of the gypsum board serves - the purpose of both absorbing heat from the molten hot melt and providing an additional barrier to the vaporized water, thus preserving the integrity of the subsequently applied hot melt coating as the hot melt solidifies.
Waxes suitable for the pre-treatment are those capable of forming a surface layer at the facing of the gypsum board.
These include paraffin and microcrystalline waxes, polyethylene waxes, Fischer-Tropsch waxes, and natural waxes, such as carnauba and candellila waxes. For the purpose of pre-treatment, the hot -~ melt curtain coating material may also be applied.
`'. , ~" 7 , ' ~.` ' . `' '' . :: ' , ~`' ` ~ . , .
Penetration of wax into the paper facing is not desir-able, in that it increases the amount of the material used without significantly increasing the beneficial effects of the treatment.
Factors which determine the degree of penetration of the wax into the paper facing include the method of application, the melting point of the wax and the temperature of the gypsum board, as dis-cussed below.
For the pre-treatment, various methods of applying the molten wax to the surface of the gypsum board, such as brushing or spraying, may be used. Of these, spraying molten wax is pre-ferred. It was found that spraying allows control over the degree of penetration of wax into the paper facing, by adjusting -the wax temperature, spraying intensity, and spraying distance.
Paraffin waxes with melting points in a range of from about 120 to about 165F and microcrystalline waxes with melting points of from about 150 to about 1930F have been found to be suitable for application at room temperature to gypsum boards.
; The applied wax blend may consist entirely of paraffin or micro-crystalline wax, or it may be a mixture of the two.
Pr -treatment of the gypsum board may take place immedi-ately after the board leaves the drying oven. In this case, the melting point of the wax or wax blend should be preferably greater than the temperature of the gypsum board. If the melting point of the wax is lower than the temperature o~ the gypsum board to be coated, excessive penetration of wax into the paper facing will occur. Consequently, proper selection of the wax or wax blend '~' ' : ' .
- ' .
2~7~3s~
with which to spray the gypsum board is important. If the temperature of the gypsum board is 1400F, then paraffin waxes with melting polnts in the range of from about 140 to about 165F or microcrystalline waxes with melting points in the range of from about 150 to about 193F may be used alone or in combination wi~h each other. Paraffin waxes with melting points lower than 140F
may be used in combination with waxes of higher melting points to produce a blend of sufficiently high melting point.
The thickness of the wax pre-treatment layer may be varied as required, but is normally in the range of from about one-half to about 10 thousandths of an inch. A thickness of from ; about 2 to about 4 thousandths of an inch is preferred. Depending on the intended application of the board, the wax layer may be applied to one or to both sides of the gypsum board. Curtain coating may take place immediately after applying the wax coating,:
or after allowing the wax coating to cool to ambient temperature.
When the surface of the board was pre-treated according to the invention, it could be observed that in some cases bubbles were absent from the subsequently applied coating, whereas in other cases bubbles trapped in the coating were noted, but the coating surface integrity was not affected. Thus, the wax layer effectively absorbs heat from the hot melt in the former cases, whereas in the latter cases it impedes expulsion of water vapour through the coating surface.
The invention will be further described by way of a ~ preferred embodiment and non-limiting examples.
.; 9 , .
- . ' i .
.'.~ ` ~
` , ' ' ' '~, . ;, .' '' '~ , `2 ~
2796~-2 ~L~ 1 An 111- X 11" piece of gypsum board was warmed in an oven to 140F, then removed from the oven and i.mmediately passed twice through a curtain coater. From the curtain coater was applied a hot melt coating having temperature of 300F and comprising a blend of 17.5% ethylene-vinyl acetate copolymer and 82.5% of paraffin having melting point o~ 140F. The coating thickness of each pass was 2 thousandths of an inch for a final thickness of ~ thousandths of an inch.
10 EXAMI?LE 2 Gypsum board was cut into 11" x 11" pieces and warmed in an oven to 140F. The boards were removed from the oven one at a time and immediately sprayed on one side with a paraffin wax having melting point of 160F, using a hand held spray gun driven by compressed nitrogen gas. The final coating thickness of the wax layer was 4 thousandths of an inch. The wax coated board was immediately curtain coated with a blend of 17.5~ ethylene-vinyl acetate copolymer and 82.5% of paraffin having melting point of 140F, at an application temperature of 300F. The thickness of the hot melt coating was 2 thousandths of an inch.
EXAMPL~ 3 A 11" x 11" piece of gypsum board having room tempera-ture was sprayed on one side with a paraffin having melting poin~
of 120F using a hand held spray gun, as in Example 2. The thick-ness of this coating was 4 thousandths of an inch. Curtain coating was carried out as in Example 1. In this case, some .
.
: . .
~; ' . .
2 ~
bubbles were no~ed in the coating, but they were retained in the coating and did not disrupt the surface integrity.
The coated gypsum boards from Examples 1, 2 and 3 were tested in a controlled environment cabinet with a relative humidity of 92~ at a temperature of 100F. To prevent the entry of water through the untreated surfaces of the board the uncoated sides of the gypsum boards were covered with a double layer of a polyethylene plastic sheet covered with a sheet of aluminium foil.
A control sample consisted of an 11" x 11" piece of gypsum board completely covered with polyethylene plastic and aluminium foil.
A reference sample was identical with samples of examples 1, 2 and 3 except that it was not pretreated with wax nor curtain coated.
The edges of the gypsum boards were sealed by dipping in a 60/40 mixture of microcrystalline wax/paraffin wax. After the samples were covered and sealed, the surface area exposed to moisture vapour was in each case nine square inches. The samples were weighed, placed in the controlled environment cabinet for twenty-four hours and weighed again. The difference between the weight after the exposure in the cabinet and the original weight constituted the water uptake. The values repor~ed in the follow-ing table are averages of at least two determinations.
~ .
.; ., . ~ . :
. ' ' '~ , ~ ' ~
:; :
~ , ~7~89 27g6~-2 5~MPL~ ~T~ ~PTAX~ (GR~M5 Control o Reference 7.3 Example 1 0.42 Example 2 0.06 Example 3 0.12 The ~ater uptake of the control demonstrates that the wrapping with polyethylene plastic and aluminum foil was effective in preventing passage of moisture. Consequently, any water uptake will have occurred through untreated surfaces, in the reference sample, or through surfaces treated in accordance with the inven-tion, in Examples 1, 2 and 3.
The results clearly demonstrate the moisture vapour ~; barrier properties of the curtain coated gypsum board (Example 1) compared with the uncoated board ~Reference), as measured by the amount of moisture penetrating into the board in the form of vapour. Examples 2 and 3 also show the effectiveness of the wax ~ pre-treatment in improving the moisture vapour barrier properties : of the curtain coating.
~, :
,'~ ' .,
Claims (30)
1. A method for coating a gypsum board to provide a gypsum board having a moisture vapour barrier layer on a surface thereof, which method comprises applying to the surface by curtain coating a hot melt of a material that will cool to form a moisture vapour barrier layer and permitting the melt to cool to form the required moisture vapour barrier layer.
2. A method according to claim 1, wherein the thickness of the barrier layer is from about one-half to about 10 thousandths of an inch.
3. A method according to claim 2, wherein the thickness of the barrier layer is from about 2 to about 4 thousandths of an inch.
4. A method according to claim 1, wherein the gypsum board consists of a core of gypsum sandwiched between two layers of paper.
5. A method according to claim 1, wherein the gypsum board consists of a core of gypsum sandwiched between two layers of glass fibre mat.
6. A gypsum board according to claim 1, wherein the barrier layer is adhered to one face of the gypsum board.
7. A gypsum board according to claim 1, wherein the barrier layer is adhered to both faces of the gypsum board.
8. A method according to claim 1, wherein the hot melt has a temperature of from about 180 to about 350°F.
9. A method according to claim 1, wherein the hot melt is applied to the gypsum board having a room temperature.
10. A method according to claim 1, wherein the hot melt is applied to the gypsum board having a temperature of about 140°F.
11. A method according to claim 1, wherein the curtain coating is effected in a single pass through a curtain coater.
12. A method according to claim 1, wherein the curtain coating is effected in a double pass through a curtain coater.
13. A method according to claim 1, wherein the moisture vapour barrier layer comprises from about 54 to about 90% paraffin wax, from 0 to about 20% microcrystalline wax, from 0 to about 25%
ethylene-vinyl acetate copolymer, from 0 to about 10% low molecu-lar weight polyethylene wax, from 0 to about 10% tackifying resins, and from 0 to about 6% styrene-rubber block copolymer.
ethylene-vinyl acetate copolymer, from 0 to about 10% low molecu-lar weight polyethylene wax, from 0 to about 10% tackifying resins, and from 0 to about 6% styrene-rubber block copolymer.
14. A method according to claim 13, wherein the moisture vapour barrier layer comprises from about 65 to about 90% paraffin wax, from about 5 to about 20% ethylene-vinyl acetate wax, from about 5 to about 10% tackifying resin, and from 0 to about 5% low molecular weight polyethylene wax.
15. A method according to claim 13, wherein the moisture vapour barrier layer further comprises an antioxidant and/or a flame retardant.
16. A method according to claim 15, wherein the antioxidant is 1,3,5-trimethyl-2,4,6-tris-(3,5-di-tert-4-hydroxybenzyl)ben-zene.
17. A method according to claim 16, wherein the antioxidant is added in an amount of from about 0.001 to about 0.1% by weight.
18. A method according to claim 17, wherein the antioxidant is added in the amount of 0.01% by weight.
19. A method according to claim 15, wherein the flame re-tardant consists of 5 parts by weight of chlorinated paraffin and 2.5 parts by weight of antimony trioxide per 100 parts by weight of the moisture vapour impermeable material.
20. A method according to claim 1, further comprising applying a wax layer to the surface of the gypsum board prior to applying the hot melt, the wax layer comprising a paraffin wax, a microcrystalline wax or a blend thereof.
21. A method according to claim 20, wherein the paraffin wax has a melting point of from about 120 to about 165°F and the microcrystalline wax has a melting point of from about 150 to about 193°F.
22. A method according to claim 20, wherein the wax layer is applied by spraying the molten wax onto the surface of the gypsum board.
23. A method according to claim 20, wherein the thickness of the wax layer is from about one-half to about 10 thousandths of an inch.
24. A method according to claim 23, wherein the thickness of the wax layer is from about 2 to about 4 thousandths of an inch.
25. A method according to claim 20, wherein the wax layer is applied to one face of the gypsum board.
26. A method according to claim 19, wherein the wax layer is applied to both faces of the gypsum board.
27. A method according to claim 20, wherein the wax layer is applied to the gypsum board having a room temperature.
28. A method according to claim 20, wherein the wax layer is applied to the gypsum board having a temperature of about 140°F.
29. A gypsum board having a moisture vapour barrier layer applied to a surface of the board by curtain coating a hot melt of a material that form the moisture vapour barrier layer when per mitted to cool.
30. A gypsum board according to claim 29 further comprising a wax layer applied to the surface of the board prior to curtain coating, the wax layer comprising a paraffin wax, a micro-crystalline wax or a blend thereof.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CA 2070489 CA2070489A1 (en) | 1992-06-04 | 1992-06-04 | Gypsum board coating |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CA 2070489 CA2070489A1 (en) | 1992-06-04 | 1992-06-04 | Gypsum board coating |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2070489A1 true CA2070489A1 (en) | 1993-12-05 |
Family
ID=4149969
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA 2070489 Abandoned CA2070489A1 (en) | 1992-06-04 | 1992-06-04 | Gypsum board coating |
Country Status (1)
| Country | Link |
|---|---|
| CA (1) | CA2070489A1 (en) |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6279284B1 (en) | 1998-01-12 | 2001-08-28 | Emco Limited | Composite vapor barrier panel |
| US20110256372A1 (en) * | 2008-08-29 | 2011-10-20 | Certainteed Gypsum, Inc. | Composite Building Boards with Thermoplastic Coatings and Cementitious Precoated Fibrous Mats |
| US20110297291A1 (en) * | 2010-06-07 | 2011-12-08 | Certainteed Gypsum, Inc. | System and Method for Constructing Composite Building Boards Using Thermoplastic Films |
| US20120308795A1 (en) * | 2008-08-29 | 2012-12-06 | Certainteed Gypsum, Inc. | Composite Floor Underlayment With Thermoplastic Coatings |
| US20130295286A1 (en) * | 2008-08-29 | 2013-11-07 | Certainteed Gypsum, Inc. | Plastic Coated Composite Building Boards and Method of Making Same |
| US9486980B2 (en) | 2010-06-07 | 2016-11-08 | Certainteed Gypsum, Inc. | Method for constructing composite building boards using dissolvable films |
| US10472293B2 (en) | 2016-04-29 | 2019-11-12 | Certainteed Gypsum, Inc. | Building assembly containing a water barrier coating film and method of making the building assembly |
| US11865820B2 (en) | 2017-12-19 | 2024-01-09 | Saint-Gobain Adfors Canada, Ltd. | Reinforcing layer, a cementitious board, and method of forming the cementitious board |
-
1992
- 1992-06-04 CA CA 2070489 patent/CA2070489A1/en not_active Abandoned
Cited By (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6279284B1 (en) | 1998-01-12 | 2001-08-28 | Emco Limited | Composite vapor barrier panel |
| US9346244B2 (en) * | 2008-08-29 | 2016-05-24 | Certainteed Gypsum, Inc. | Composite building boards with thermoplastic coatings and cementitious precoated fibrous mats |
| US20110256372A1 (en) * | 2008-08-29 | 2011-10-20 | Certainteed Gypsum, Inc. | Composite Building Boards with Thermoplastic Coatings and Cementitious Precoated Fibrous Mats |
| US20120308795A1 (en) * | 2008-08-29 | 2012-12-06 | Certainteed Gypsum, Inc. | Composite Floor Underlayment With Thermoplastic Coatings |
| US20130295286A1 (en) * | 2008-08-29 | 2013-11-07 | Certainteed Gypsum, Inc. | Plastic Coated Composite Building Boards and Method of Making Same |
| US10767368B2 (en) * | 2008-08-29 | 2020-09-08 | Certainteed Gypsum, Inc. | Plastic coated composite building boards and method of making same |
| US9186869B2 (en) * | 2008-08-29 | 2015-11-17 | Certainteed Gypsum, Inc. | Composite floor underlayment with thermoplastic coatings |
| US9885179B2 (en) * | 2008-08-29 | 2018-02-06 | Certainteed Gypsum, Inc. | Plastic coated composite building boards and method of making same |
| US20180187416A1 (en) * | 2008-08-29 | 2018-07-05 | Certainteed Gypsum, Inc. | Plastic Coated Composite Building Boards and Method of Making Same |
| US9259888B2 (en) * | 2008-08-29 | 2016-02-16 | Certainteed Gypsum, Inc. | Plastic coated composite building boards and method of making same |
| US20110297291A1 (en) * | 2010-06-07 | 2011-12-08 | Certainteed Gypsum, Inc. | System and Method for Constructing Composite Building Boards Using Thermoplastic Films |
| US9486980B2 (en) | 2010-06-07 | 2016-11-08 | Certainteed Gypsum, Inc. | Method for constructing composite building boards using dissolvable films |
| US10457027B2 (en) | 2010-06-07 | 2019-10-29 | Certainteed Gypsum, Inc. | System and method for constructing composite building boards using thermoplastic films |
| US9096036B2 (en) * | 2010-06-07 | 2015-08-04 | Certainteed Gypsum, Inc. | System and method for constructing composite building boards using thermoplastic films |
| US10472293B2 (en) | 2016-04-29 | 2019-11-12 | Certainteed Gypsum, Inc. | Building assembly containing a water barrier coating film and method of making the building assembly |
| US11865820B2 (en) | 2017-12-19 | 2024-01-09 | Saint-Gobain Adfors Canada, Ltd. | Reinforcing layer, a cementitious board, and method of forming the cementitious board |
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