CA2427514A1 - Drywall tape and joint - Google Patents
Drywall tape and joint Download PDFInfo
- Publication number
- CA2427514A1 CA2427514A1 CA002427514A CA2427514A CA2427514A1 CA 2427514 A1 CA2427514 A1 CA 2427514A1 CA 002427514 A CA002427514 A CA 002427514A CA 2427514 A CA2427514 A CA 2427514A CA 2427514 A1 CA2427514 A1 CA 2427514A1
- Authority
- CA
- Canada
- Prior art keywords
- drywall
- joint
- tape
- web
- coating
- 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
- 239000011499 joint compound Substances 0.000 claims abstract description 71
- 238000000576 coating method Methods 0.000 claims abstract description 67
- 239000011248 coating agent Substances 0.000 claims abstract description 58
- 239000000853 adhesive Substances 0.000 claims abstract description 36
- 239000003365 glass fiber Substances 0.000 claims abstract description 35
- 239000011230 binding agent Substances 0.000 claims abstract description 34
- 230000001070 adhesive effect Effects 0.000 claims abstract description 32
- 238000000034 method Methods 0.000 claims abstract description 16
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 28
- 229920002689 polyvinyl acetate Polymers 0.000 claims description 22
- 239000004820 Pressure-sensitive adhesive Substances 0.000 claims description 21
- 239000011118 polyvinyl acetate Substances 0.000 claims description 21
- 239000004744 fabric Substances 0.000 claims description 19
- 239000000203 mixture Substances 0.000 claims description 18
- 239000002981 blocking agent Substances 0.000 claims description 14
- 229920005989 resin Polymers 0.000 claims description 14
- 239000011347 resin Substances 0.000 claims description 14
- 229920003048 styrene butadiene rubber Polymers 0.000 claims description 13
- 239000002174 Styrene-butadiene Substances 0.000 claims description 12
- 230000008439 repair process Effects 0.000 claims description 12
- 150000001875 compounds Chemical class 0.000 claims description 11
- 239000000839 emulsion Substances 0.000 claims description 10
- 239000000463 material Substances 0.000 claims description 10
- 239000003292 glue Substances 0.000 claims description 9
- 239000007788 liquid Substances 0.000 claims description 9
- 239000004372 Polyvinyl alcohol Substances 0.000 claims description 8
- 229920000058 polyacrylate Polymers 0.000 claims description 8
- 229920002451 polyvinyl alcohol Polymers 0.000 claims description 8
- 229920001577 copolymer Polymers 0.000 claims description 7
- 238000001035 drying Methods 0.000 claims description 5
- 229920002472 Starch Polymers 0.000 claims description 4
- 229920006243 acrylic copolymer Polymers 0.000 claims description 4
- 238000005304 joining Methods 0.000 claims description 4
- 239000007787 solid Substances 0.000 claims description 4
- 235000019698 starch Nutrition 0.000 claims description 4
- 239000008107 starch Substances 0.000 claims description 4
- 238000009736 wetting Methods 0.000 claims description 4
- 108010010803 Gelatin Proteins 0.000 claims description 3
- 229920000715 Mucilage Polymers 0.000 claims description 3
- 239000004793 Polystyrene Substances 0.000 claims description 3
- 108010073771 Soybean Proteins Proteins 0.000 claims description 3
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 claims description 3
- 239000008273 gelatin Substances 0.000 claims description 3
- 229920000159 gelatin Polymers 0.000 claims description 3
- 235000019322 gelatine Nutrition 0.000 claims description 3
- 235000011852 gelatine desserts Nutrition 0.000 claims description 3
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 claims description 3
- 229920002223 polystyrene Polymers 0.000 claims description 3
- 229920000915 polyvinyl chloride Polymers 0.000 claims description 3
- 239000004800 polyvinyl chloride Substances 0.000 claims description 3
- 108090000623 proteins and genes Proteins 0.000 claims description 3
- 102000004169 proteins and genes Human genes 0.000 claims description 3
- 229940001941 soy protein Drugs 0.000 claims description 3
- 239000011115 styrene butadiene Substances 0.000 claims description 3
- 239000000126 substance Substances 0.000 claims description 3
- 235000013311 vegetables Nutrition 0.000 claims description 3
- 230000006872 improvement Effects 0.000 claims description 2
- 229920000591 gum Polymers 0.000 claims 2
- 150000002484 inorganic compounds Chemical class 0.000 claims 2
- 229910010272 inorganic material Inorganic materials 0.000 claims 2
- 239000004745 nonwoven fabric Substances 0.000 claims 2
- 239000002759 woven fabric Substances 0.000 claims 2
- 238000010276 construction Methods 0.000 abstract description 8
- 239000011521 glass Substances 0.000 description 16
- 210000001503 joint Anatomy 0.000 description 16
- 239000010440 gypsum Substances 0.000 description 13
- 229910052602 gypsum Inorganic materials 0.000 description 13
- 239000000835 fiber Substances 0.000 description 12
- 238000009472 formulation Methods 0.000 description 11
- 239000010410 layer Substances 0.000 description 10
- 229920001971 elastomer Polymers 0.000 description 7
- 239000004816 latex Substances 0.000 description 7
- 229920000126 latex Polymers 0.000 description 7
- 230000008569 process Effects 0.000 description 7
- 238000012360 testing method Methods 0.000 description 7
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 6
- 239000000123 paper Substances 0.000 description 6
- 239000005060 rubber Substances 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 5
- 238000009864 tensile test Methods 0.000 description 5
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- 239000002131 composite material Substances 0.000 description 4
- 239000012943 hotmelt Substances 0.000 description 4
- 239000002655 kraft paper Substances 0.000 description 4
- 239000012188 paraffin wax Substances 0.000 description 4
- 239000001993 wax Substances 0.000 description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 3
- 239000004698 Polyethylene Substances 0.000 description 3
- 230000032798 delamination Effects 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- 239000011152 fibreglass Substances 0.000 description 3
- 239000000945 filler Substances 0.000 description 3
- 239000010408 film Substances 0.000 description 3
- 229920001519 homopolymer Polymers 0.000 description 3
- 239000003973 paint Substances 0.000 description 3
- -1 polyethylene Polymers 0.000 description 3
- 229920000573 polyethylene Polymers 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 230000003014 reinforcing effect Effects 0.000 description 3
- 229920006395 saturated elastomer Polymers 0.000 description 3
- 239000011503 setting type joint compound Substances 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- 230000000903 blocking effect Effects 0.000 description 2
- ZOMBKNNSYQHRCA-UHFFFAOYSA-J calcium sulfate hemihydrate Chemical compound O.[Ca+2].[Ca+2].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O ZOMBKNNSYQHRCA-UHFFFAOYSA-J 0.000 description 2
- 239000004202 carbamide Substances 0.000 description 2
- 239000004568 cement Substances 0.000 description 2
- 239000004567 concrete Substances 0.000 description 2
- 238000005336 cracking Methods 0.000 description 2
- 239000011094 fiberboard Substances 0.000 description 2
- 238000011049 filling Methods 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 230000002787 reinforcement Effects 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- 229920001909 styrene-acrylic polymer Polymers 0.000 description 2
- 229920001169 thermoplastic Polymers 0.000 description 2
- 239000004416 thermosoftening plastic Substances 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- WZZBNLYBHUDSHF-DHLKQENFSA-N 1-[(3s,4s)-4-[8-(2-chloro-4-pyrimidin-2-yloxyphenyl)-7-fluoro-2-methylimidazo[4,5-c]quinolin-1-yl]-3-fluoropiperidin-1-yl]-2-hydroxyethanone Chemical compound CC1=NC2=CN=C3C=C(F)C(C=4C(=CC(OC=5N=CC=CN=5)=CC=4)Cl)=CC3=C2N1[C@H]1CCN(C(=O)CO)C[C@@H]1F WZZBNLYBHUDSHF-DHLKQENFSA-N 0.000 description 1
- CGLQOIMEUPORRI-UHFFFAOYSA-N 2-(1-benzoyloxypropan-2-yloxy)propyl benzoate Chemical compound C=1C=CC=CC=1C(=O)OCC(C)OC(C)COC(=O)C1=CC=CC=C1 CGLQOIMEUPORRI-UHFFFAOYSA-N 0.000 description 1
- DXPPIEDUBFUSEZ-UHFFFAOYSA-N 6-methylheptyl prop-2-enoate Chemical compound CC(C)CCCCCOC(=O)C=C DXPPIEDUBFUSEZ-UHFFFAOYSA-N 0.000 description 1
- 229920002126 Acrylic acid copolymer Polymers 0.000 description 1
- 229920001817 Agar Polymers 0.000 description 1
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- 229920001353 Dextrin Polymers 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 229920002907 Guar gum Polymers 0.000 description 1
- 239000004831 Hot glue Substances 0.000 description 1
- 239000011398 Portland cement Substances 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000002390 adhesive tape Substances 0.000 description 1
- 239000008272 agar Substances 0.000 description 1
- 235000010443 alginic acid Nutrition 0.000 description 1
- 229920000615 alginic acid Polymers 0.000 description 1
- 239000010775 animal oil Substances 0.000 description 1
- 230000003466 anti-cipated effect Effects 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 230000000712 assembly Effects 0.000 description 1
- 238000000429 assembly Methods 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- DQXBYHZEEUGOBF-UHFFFAOYSA-N but-3-enoic acid;ethene Chemical compound C=C.OC(=O)CC=C DQXBYHZEEUGOBF-UHFFFAOYSA-N 0.000 description 1
- 238000001354 calcination Methods 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 235000014633 carbohydrates Nutrition 0.000 description 1
- 150000001720 carbohydrates Chemical class 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000000679 carrageenan Substances 0.000 description 1
- 235000010418 carrageenan Nutrition 0.000 description 1
- 229920001525 carrageenan Polymers 0.000 description 1
- 229940113118 carrageenan Drugs 0.000 description 1
- 239000005018 casein Substances 0.000 description 1
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
- 235000021240 caseins Nutrition 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- FYGDTMLNYKFZSV-MRCIVHHJSA-N dextrin Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)OC1O[C@@H]1[C@@H](CO)OC(O[C@@H]2[C@H](O[C@H](O)[C@H](O)[C@H]2O)CO)[C@H](O)[C@H]1O FYGDTMLNYKFZSV-MRCIVHHJSA-N 0.000 description 1
- 150000004683 dihydrates Chemical class 0.000 description 1
- 239000011501 drying type joint compound Substances 0.000 description 1
- 239000000806 elastomer Substances 0.000 description 1
- 229920001038 ethylene copolymer Polymers 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 150000004676 glycans Chemical class 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 239000000665 guar gum Substances 0.000 description 1
- 235000010417 guar gum Nutrition 0.000 description 1
- 229960002154 guar gum Drugs 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 238000009940 knitting Methods 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000004570 mortar (masonry) Substances 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000011297 pine tar Substances 0.000 description 1
- 229940068124 pine tar Drugs 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 235000019353 potassium silicate Nutrition 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 235000018102 proteins Nutrition 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 239000005061 synthetic rubber Substances 0.000 description 1
- PZTAGFCBNDBBFZ-UHFFFAOYSA-N tert-butyl 2-(hydroxymethyl)piperidine-1-carboxylate Chemical compound CC(C)(C)OC(=O)N1CCCCC1CO PZTAGFCBNDBBFZ-UHFFFAOYSA-N 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
- 238000009941 weaving Methods 0.000 description 1
- UHVMMEOXYDMDKI-JKYCWFKZSA-L zinc;1-(5-cyanopyridin-2-yl)-3-[(1s,2s)-2-(6-fluoro-2-hydroxy-3-propanoylphenyl)cyclopropyl]urea;diacetate Chemical compound [Zn+2].CC([O-])=O.CC([O-])=O.CCC(=O)C1=CC=C(F)C([C@H]2[C@H](C2)NC(=O)NC=2N=CC(=CC=2)C#N)=C1O UHVMMEOXYDMDKI-JKYCWFKZSA-L 0.000 description 1
Classifications
-
- E—FIXED CONSTRUCTIONS
- E04—BUILDING
- E04F—FINISHING WORK ON BUILDINGS, e.g. STAIRS, FLOORS
- E04F13/00—Coverings or linings, e.g. for walls or ceilings
- E04F13/02—Coverings or linings, e.g. for walls or ceilings of plastic materials hardening after applying, e.g. plaster
- E04F13/04—Bases for plaster
- E04F13/042—Joint tapes
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J7/00—Adhesives in the form of films or foils
- C09J7/20—Adhesives in the form of films or foils characterised by their carriers
- C09J7/22—Plastics; Metallised plastics
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06N—WALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
- D06N3/00—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof
- D06N3/0002—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof characterised by the substrate
- D06N3/0015—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof characterised by the substrate using fibres of specified chemical or physical nature, e.g. natural silk
- D06N3/0022—Glass fibres
-
- E—FIXED CONSTRUCTIONS
- E04—BUILDING
- E04F—FINISHING WORK ON BUILDINGS, e.g. STAIRS, FLOORS
- E04F13/00—Coverings or linings, e.g. for walls or ceilings
- E04F13/02—Coverings or linings, e.g. for walls or ceilings of plastic materials hardening after applying, e.g. plaster
- E04F13/04—Bases for plaster
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06N—WALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
- D06N2205/00—Condition, form or state of the materials
- D06N2205/02—Dispersion
- D06N2205/023—Emulsion, aqueous dispersion, latex
Landscapes
- Engineering & Computer Science (AREA)
- Architecture (AREA)
- Civil Engineering (AREA)
- Structural Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Textile Engineering (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Adhesive Tapes (AREA)
- Laminated Bodies (AREA)
- Building Environments (AREA)
- Paints Or Removers (AREA)
Abstract
Drywall tapes, drywall joints and methods for their construction are provided by this invention. The drywall tape of this invention includes a web of glass fibers and a coating disposed over a portion of the glass fibers. The coating includes a resinous binder which is at least partially soluble or dispersible in joint compound. The resinous binder is capable of forming an adhesive bond with the joint compound when set.
Description
DRYWALL TAPE AND JOINT
Field of the Invention S (0001] The present invention relates to drywall joining systems for seams or repairs generally, and more particularly to tape used for drywall installation and repairs.
Background of the Invention [0002] Walls made from gypsum wall board or drywall are conventionally constructed by affixing the boards to studs or joints and filling and coating the joints with a specially prepared adhesive called "joint compound." This process is also used to make repairs of defects, such as holes and dents, including those around electrical boxes, piping and duct work, as well as corners created by the intersection of drywall boards.
Field of the Invention S (0001] The present invention relates to drywall joining systems for seams or repairs generally, and more particularly to tape used for drywall installation and repairs.
Background of the Invention [0002] Walls made from gypsum wall board or drywall are conventionally constructed by affixing the boards to studs or joints and filling and coating the joints with a specially prepared adhesive called "joint compound." This process is also used to make repairs of defects, such as holes and dents, including those around electrical boxes, piping and duct work, as well as corners created by the intersection of drywall boards.
[0003] Drywall tape adds strength and crack resistance as well as smooth concealment at flat joints and inside corners. Conventionally, two types of drywall tape have been employed - a simple kraft paper strip which is adhered to the drywall surfaces by a bedding coat of joint compound or "mud," and glass fiber tape, which can be applied with joint compound or self-adhered. Kraft paper tape must be carefully positioned a~ad care must be taken not to discharge the mud onto non-working surfaces. In addition, once the paper drywall tape has been applied, one must wait as much as a day for the compound to dry before a final surface coat of compound can be applied. Glass fiber tape, on the other hand, provides exceptional wet and dry strength and resists stretching and wrinl,;les. It can be laid flat and resists tearing under load.
[0004] A joint treatment system which includes reinforcing tape and joint compound, must provide joints as strong as the gypsum board itself. Otherwise, normal stmctural movement in the wall or ceiling assembly can result in the development of cracl<a over the finished joins.
PH 11897635.1 [0005] It has been discovered that certain types of fiberglass leno-weave mesh tape when used with conventional joint compounds are more prone to cracking than joints finished with paper tape and conventional joint compounds. Because of this, some manufacturers, such as United States Gypsum Company, Chicago, Illinois, have manufactured glass fiber tapes with cross-fiber construction to provide greater drywall joint strength than conventional fiberglass leno-weave mesh tapes. Such tapes include Sheetrock~
brand fiberglass drywall tape and Imperial~ brand tape. The Imperial~ brand tape includes an open weave of glass fibers (100 meshes per square inch) which is coated with a binder and slit to roll width. Spirally woven (leno) long strands and the binder coating reduce edge raveling and fraying and keep the loose threads from defacing finishing surfaces.
PH 11897635.1 [0005] It has been discovered that certain types of fiberglass leno-weave mesh tape when used with conventional joint compounds are more prone to cracking than joints finished with paper tape and conventional joint compounds. Because of this, some manufacturers, such as United States Gypsum Company, Chicago, Illinois, have manufactured glass fiber tapes with cross-fiber construction to provide greater drywall joint strength than conventional fiberglass leno-weave mesh tapes. Such tapes include Sheetrock~
brand fiberglass drywall tape and Imperial~ brand tape. The Imperial~ brand tape includes an open weave of glass fibers (100 meshes per square inch) which is coated with a binder and slit to roll width. Spirally woven (leno) long strands and the binder coating reduce edge raveling and fraying and keep the loose threads from defacing finishing surfaces.
[0006] Still another drywall tape that has been commercially accepted is Fibatape~ glass tape available through San Gobain Technical Fabrics, Ontario, Canada. This product is an SBR rubber-coated glass fiber tape with a self-adhesive backing. The tape is self-adhered to a drywall seam, and then covered with layers of drywall compound.
Samples of a drywall joint made with Fibatape~ tape have been tensile tested in accordance with ASTM C 474 (Appendix) which measures the strength to first crack of a tape-compound sample coated in electrically conductive paint. The strength is measured until the first crack in the paint occurs, which breaks the electrical continuity along the surface and registers the ultimate tensile load. Failure in Fibatape~ joint tape tensile specimens is observed at the SBR rubber film where the joint compound separates from the film at failure. This suggests that typical taped joints in glass tape-drywall systems do not optimize the strength of the glass joint compound composite, since tensile loads tend to separate the glass fibers from the joint compound matrix instead of transferring these loads to the glass fibers themselves.
Samples of a drywall joint made with Fibatape~ tape have been tensile tested in accordance with ASTM C 474 (Appendix) which measures the strength to first crack of a tape-compound sample coated in electrically conductive paint. The strength is measured until the first crack in the paint occurs, which breaks the electrical continuity along the surface and registers the ultimate tensile load. Failure in Fibatape~ joint tape tensile specimens is observed at the SBR rubber film where the joint compound separates from the film at failure. This suggests that typical taped joints in glass tape-drywall systems do not optimize the strength of the glass joint compound composite, since tensile loads tend to separate the glass fibers from the joint compound matrix instead of transferring these loads to the glass fibers themselves.
[0007] Accordingly, there is a need for creating a higher strength wall board joint composite system employing glass fiber tape. Such a system should be chemically FH 1 X897635.1 compatible with ready mixed or powder joint compound compositions and should not substantially detract from the already established benefits of using glass fiber tape over kraft paper tape.
Summarlr of the Invention [0008] In a first embodiment of the present invention, a drywall tape suitable for joint compound repairs and joint covering is provided. The drywall tape includes a web of glass fibers and a coating disposed over a portion of the glass fibers. The coating comprises a resinous binder which is at least partially soluble or dispersible in the joint compound. The coating is further capable of forming an adhesive bond with the joint compound when set.
Summarlr of the Invention [0008] In a first embodiment of the present invention, a drywall tape suitable for joint compound repairs and joint covering is provided. The drywall tape includes a web of glass fibers and a coating disposed over a portion of the glass fibers. The coating comprises a resinous binder which is at least partially soluble or dispersible in the joint compound. The coating is further capable of forming an adhesive bond with the joint compound when set.
[0009] In the preferred embodiments, the joint compound and re-wettable coating "wet and set" together. The re-wettable coating can be chemically very similar to the binding resin that makes up the compound itself, or is at least soluble or dispersible in the joint compound. Most preferably, the re-wettable coating is soluble or dispersible in the water content of the joint compound so that it flows together with the compound on a microscopic scale. Once dry, the coating most preferably becomes a very rigid film that is well able to transfer loads from the joint compound to the fiber. This permits the joint compound and drywall tape of this invention to act much like a fully integrated composite, which increases the mechanical properties of the joint.
[0010] Tensile testing of joints made in accordance with this invention has revealed that the load to first crack can be increased by as much as 16 to 65% over SBR-coated Fibatape samples embedded in the same joint compound composition. Note that all samples were coated on one side with a pressure sensitive adhesive. Testing of plant production samples in accordance with ASTM C474 (appendix) revealed that leno weave fabrics benefitted most by the new coating, with a 65% improvement, followed by knit PHl1897635. I
fabric (40%) and lastly, plain weaves (16 to 28%). When tapes without an adhesive backing are tested in accordance with ASTM C474, a similar percent increase in tensile load to failure can be attributed to the invention. However, the magnitude of the results will be about double that of the tapes that are adhesive backed. The explanation for this is that, in the case of the adhesive coated samples, half of the surface area of the glass web IO would be covered with a layer of low modulus pressure-sensitive material that does little to resist tensile loads placed on the sample.
[OOI 1] While standard glass tape products typically fail due to the fiber pulling out from the joint compound, the drywall tape of this invention with the re-wettable coating has been shown to fail by delamination within the joint compound itself. Along with the increased load to tensile failure, delamination in the joint compound suggests that the bond between the coating and the compound is improved since the fibers in the sample do not pull out. The drywall tape of this invention also produces tensile strength results which are approximately twice those previously measured for paper tape, without adding anymore basis weight or fibers to the glass fabric, over that for a conventional glass tape, such as Fibatape~ tape.
[0012] In further embodiments of this invention, the re-wettable coating comprises a soluble or dispersible resinous binder alone, or in combination with a blocking agent, such as a wax. A combination of a soluble binder, such as polyvinyl acetate (PVAc), and wax, offers a strong bond with the joint compound, while also minimizing "blocking" in the tape. The preferred re-wettable coating contains PVAc resin which is very hydroscopic. Water vapor absorption can cause a roll of tape made with PVAc resin to block or fuse together, which causes the roll to bind. The roll of tape can also flow plastically and deform the shape of the tape roll. Blocking agents, such as paravffin wax, make the PVAc-based coating vapor resistant. Only when contacted with liquid water, PH 1 X897635. I
5 such as when the tape is applied to a wall and coated with joint compound, does the PVAc resin re-wet and become soluble.
[0013] In a further embodiment of this invention, a method is provided for preparing a drywall joint. The method includes disposing a pair of drywall boards in adjoining relationship to one another to form a seam region. Next, the drywall tape of this invention is disposed over the seam. This drywall tape includes a web of glass fibers having disposed thereon a resinous binder capable of re-wetting and setting when contacted with the joint compound. A first joint compound layer is applied over the drywall tape so as to re-wet the resinous binder. The first joint compound layer ;and re-wetted resinous binder on the tape are then dried to form an adhesive bond.
Brief Description of the Drawings [0014] The accompanying drawings illustrate preferred embodiments of the invention according to the practical application of the principles thereof, and in which:
[0015] FIG. 1: is a partial, front perspective view of the preferred drywall tape of this invention;
[0016] FIG. 2: is a partial, enlarged side-plan view, illustrating a coating on the drywall tape of FIG. 1;
[0017] FIG. 3: is a partial, top, cross-sectional view of a finished flat drywall joint of this invention; and [0018] FIG. 4: is a graphical depiction of the average load to first crack for various drywall tape constructions, including those of the present invention.
Detailed Description of the Invention [0019) This invention provides drywall tape, drywall joints, methods of preparing drywall joints, and reinforcements for cementitious materials generally. It is understood that PH 11897635. I
while the present invention is preferably related to drywall seam or repair constructions, the re-wettable coatings on the glass and other reinforcing fibrous webs provide practical solutions to reinforcing gypsum fiber board, gypsum wall board, glass-faced gypsum board, tilebacker boards, high impact gypsum wall board, and concrete board constructions. The re-wettable coatings of this invention can be useful with cementitious materials such as gypsum, portland cement, and combinations of these materials with fillers or aggregate, such as mortar, cement and concrete. This invention can be used to enhance the performance of existing self adhesive drywall joint tapes and patches, or tapes and patches which do not have a pressure-sensitive adhesive on one side of their construction. The benefits of a re-wettable resinous binder are realized whether a pressure-sensitive adhesive is present on the web or not. As used herein, the team "drywall" includes wall board, fiberboard, glass-faced gypsum boards, and their-equivalents. As used herein, the term "tape" means a strip of material that can be provided in roll form, which may, or may not, contain an adhesive backing layer.
[0020] With regard to the figures, and particularly to FIGS. 1-2 thereof, there is shown a preferred drywall tape 100 including a web of glass fibers 10 and an optional pressure-sensitive adhesive layer 12. When a portion of the drywall tape 100 is magnified, as shown in FIG. 2, the re-wettable coating 14 can be viewed. In the preferred embodiment of the drywall tape 100, the re-wettable coating 14 is disposed along one or bath sides of the web of glass fibers 10. Alternatively, the re=wettable coating 14 can be di;;posed over 100% of the exterior surfaces of the web of glass fibers 10, over 70% of the surface area, or over less than SO% of the surface area. In certain constructions, the glass fibers of the web of glass fibers 10 are bonded together using a web adhesive binder 15, such as vinyl acetate acrylic, styrene/acrylate, vinyUacetate, acrylic, styrene acrylic, or copolymers and mixtures thereof, ete. In instances where a web adhesive binder 15 is employed, it may or may not be re-wettable, soluble or dispersible in liquid water. In the preferred PH 11897635.1 embodiment, the re-wettable coating 14 is used to also bind the fibers of the web of glass fibers together.
[0021] As shown in FIG. 3, a flat drywall joint can be constructed by butt joining a pair of drywall boards 18 and 17 to form a seam region 45. The drywall tape 100 can be applied with the aid of the pressure-sensitive adhesive Iayer 12, or when a pressure-sensitive adhesive is not employed, the drywall tape 100 can be pressed lightly into a wet joint compound layer which is thinly applied to the seam region 45 prior to application of the drywall tape 100. If joint compound is used to adhere the drywall tape 100 to the seam region 45, care must be taken to provide sufficient joint compound under t)he tape to prevent blistering of the tape. While embedding the tape 100, excess joint compound should be removed from the edge.
(0022] Whether the tape 100 is applied with joint compound, or self-adhered, a first coat of joint compound 30 should applied over the tape so as to embed the tape 100 nearly completely. While embedding the tape 100, excess joint compound is removed from the edge. Added water can be included in the joint compound so as to thin it for ea:~ier application. Similar approaches can be provided for inside corners, outside corners, horizontal flat joints and hole and crack repairs, finished seams along electrical boxes and switches and seams around piping and duct work.
[0023] After the first coat 30 is allowed to dry, preferably overnight, a second coat 40 of drywall compound is applied over the first coat 30, ideally with an 8 inch knife., feathering slightly beyond the first coat. If further coats are desired, the second coat 40 is allowed to dry, and a third or finishing coat (not shown) can be applied with a 1.0 inch knife to the flat joints. The second coat 40 or third coat can be lightly sanded if necessary.
[0024] The joint compound useful in the drywall joints of this invention is typically classified as either a "drying" or "setting" type. In a drying-type joint compound, the PH 0897635.1 S filler comprises substantially calcium carbonate. Prior to use, the filler and the binder, along with several other known ingredients, are mixed with water. After application, when the water drys to evaporation, a dry, relatively hard cementitious material is left behind.
[0025] Joint compositions known as the "setting" type include at least a substantial portion of calcium sulfate hemihydrate. In order to produce calcined gypsum, one converts calcium sulfate dihydrate from raw gypsum to the hemihydrate state through a known process called calcination. This process removes 1 ~h molecules of water from the calcium sulfate dihydrate gypsum. The hemihydrate form of calcium sulfate is substantially more soluble in water than the dihydxate form of calcium sulfate. wring 1S use of a setting-type joint compound, the calcium sulfate hemihydrate is rehydrated to the dihydrate state. This rehydration process normally takes place over a fairly short period of time. Accordingly, it is extremely difficult to produce a setting-type joint compound for storage in a bucket, and as such, such compounds are typically provided in powder form. Setting-type joint compounds also form a crystalline network upon setting, and provide a stronger, more durable bond.
[0026] The webs useful in manufacturing the drywall tape I00 of this invention can be provided as non-woven, woven or knitted fabrics, veils, mats, scrims, or fleece. They desirably include high strength fibers, such as glass fiber, and less desirably may include thermoplastic or thermosetting fibers, carbon, boron, graphite fibers or combinations 2S thereof. In most examples of this invention, a web of glass fibers 10 having a basis weight of about S-500 grams/m', preferably about 20-120 grams/m2, is employed.
This web 10 can be fabricated by weaving, such as a plane or leno weave, by knitting, by a laid scrim process or by a non-woven process, such as resin bonding randomly oriented glass fibers. The webs of this invention are, desirably, at least partially porous to wca joint compound so as to form a good bond in the seam region 4S. Alternatively, a veil or PH 11897635.1 fabric could be somewhat non-porous to joint compound and still be useful as a replacement for paper tape and, thus, be applied with a bedding coat of joint compound.
[0027] The preferred re-wettable coating 14 applied to the web desirably has the properties of being soluble or dispersible in liquid water. Glass tapes of the past were often coated with polymers, such as SBR rubber or a resinous binder, such as virnyl acetate acrylic, styrene/acrylate, vinyUacetate, acrylic, styrene acrylic, etc., which wee specifically designed to aid in handling and slitting the reinforcements without regard to how the coatings interacted with joint compounds. The adhesion of traditional rubber based coatings such as SBR to setting or non-setting joint compounds is minimal, and thus, an optimum composite strength cannot be achieved, e.g., the glass fibers tend to pull out from compound when loaded. The preferred re-wettable coatings 14 of this invention set to form a strong bond between the preferred glass fibers and the set joint compound so that the fibers act more as an unit to resist loads. The preferred re-wettable coating 14 of this invention should be as inexpensive as the styrene butadiene rubber (SBR) or joining resin binders currently employed on glass drywall tape. This coating 14 should be easy and versatile to formulate and should run on pad rolls with water clean up being; highly desirable. It should not be significantly prone to oxidation or W light degradation.
Ideally, the preferred re-wettable coating 14 i.s provided in a latex form such as an aqueous emulsion of a binder resin, blocking agent and water.
[0028] The preferred re-wettable coating 14 of this invention contains one or more of the resins selected from the group including: polyvinyl acetate, ethylene vinyl acetate, polystyrene, polyvinyl chloride, polyacrylate, ethylene acetate co-polymer, vinyl-acrylic co-polymer, styrene butadiene, acrylic polymer and starch; protein glues, such as casein, soy protein, animal glue and gelatin; vegetable-based glues, such as cellulosics and their chemically modified derivatives; gums (polysaccharides and carbohydrates) such as guar gum; resins (pine tar) which may not be water soluble; mucilages (agar, carrageenan and PH 1897635.1 5 algin); inorganics such as soluble silicates (water glass) and cementitious materi<ils (cement, gypsum), and co-polymers and combinations of these. Most preferably, the resinous binder contains polyvinyl acetate (PVAc), such as Vinac 524 polyvinyl acetate homopolymer stabilized with polyvinyl alcohol, Airflex 401 polyvinyl acetateJethylene co-polymer stabilized with polyvinyl alcohol, both supplied by Air Products and 10 Chemicals, Inc., of 7201 Hamilton Blvd., Allentown, PA 18195. The re-wettable coating 14 preferably is provided in an aqueous emulsion or solution containing about 2.5-75 wt.
% solids. Alternatively, water soluble polymers in powder form may be applied with adhesive or electrostatically. Two formulations of the re-wettable coating developed within the context of this invention are found below:
(0029] Formulation 1 Vinac 524 Emulsion (PVAc homopolymer stabilized with polyvinyl alcohol) 61.38%
Airflex 40I Emulsion (PVAc/ethylene co-polymer stabilized with polyvinyl alcohol 26.30'%
Water 9.02%
Urea 0.25%
Hydrocer DP69 (paraffin wax, anti-blocking agent) 3.00%
900-103 Henkel Foamaster NXZ mixed 50/50% with water. 0.05%
Other pertinent formula data:
Solids level: 50%
Viscosity: about 1000 cps PH: approximately 6.0 f'H 11897635.1 S [0030] Formulation 2 Vinac S24 Emulsion (PVAc homopolymer 74.53%
stabilized with polyvinyl alcohol) Benzoflex 9-88 (dipropylene glycol dibenzoate plasticizer for PVAc) 7.23%
Urea 0.25%
Hydrocer DP69 (paraffin wax, anti-blocking agent) 3.00%~
Water 14.94°!~
900-103 Henkel Foamaster NXZ mixed SO/SO% with water O.OS%~
(0031] As reflected above, an important ingredient for preventing the PVAc resin from picking up too much water during storage is an anti-blocking agent, such as animal oils, fats, starch, dextrine, silicone oil, waxes and combinations thereof. The preferred anti-blocking agent is low melting point paraffin wax. The paraffin wax can be emulsified in the formulations and "blooms" to the surface when the formation is dried. The blocking agent acts as a vapor burner to the re-wettable 14 coating on the drywall tape 100 of this invention, so as to substantially reduce blocking in tape rolls. The anti-blocking agent should be less than about S-10% by weight of the formulation so that it can be dispersed readily when the re-wettable coating 14 is made soluble by the water in the joint compound. Accordingly, the re-wettable coating 14 with the above formulations containing an anti-blocking agent and PVAc resin in solution, is capable of being vapor resistant when dry, but is water soluble or dispersible when contacted with liquid water in the joint compound.
[0032] The adhesive elements of this invention can be made of any known pressure-sensitive adhesive material. As used herein, the term "pressure-sensitive"
refers to any releasable adhesive or releasable tenacious means. Adhesive compositions suitable for tape include, for example, the water-based pressure-sensitive adhesive such as acrylate adhesives, e.g., isooctyl acrylate and acrylic acid copolymer, or vinyl acetate-2 ethyl hexyl acrylate copolymer which can be combined with tackifiers. Alternatively, the adhesive PHl897635.t may comprise the rapid setting thermoplastic "hot melt" adhesives. The adhesive elements may also comprise a two-sided adhesive tape. It is also anticipated that.
adhesives based on an elastomer selected from natural or synthetic rubbers could be used.
It will be understood that alternative shapes for these adhesives, for examples, continuous coatings, discontinuous lines, squares, dots, circles, etc., may be employed.
IO [0033] The preferred method of manufacturing the drywall tape I00 of this invention shall now be described. The glass fabric knitted web of 42.1 - 52.9 grams/m2 is first passed through a bath of latex including the Formulations 1 or 2 and then through a set of squeeze rollers, which sen~e to control the amount of latex picked up by the fab>-ic, usually about 5-20 grams/m2 of coating when dry. The rollers could be adjusted for gap width or pressure to perform this function, but the solids level and the viscosity of the latex are important factors in determining the coating weight. The saturated fabric is then dried either by contact with steam cans or by convection in a hot oven.
[0034] At this point, the web of glass fibers 10, now coated with a re-wettable coating I4, is provided with a pressure sensitive adhesive layer 12 applied to one side, usually about 3-15 grams/m' of adhesive is applied. This may be done in a subsequent step on a separate finishing machine, or directly in line with the re-wettable coating step. The pressure-sensitive adhesive layer 12 serves to affix the drywall tape 100 to the drywall surface in preparation for drywall filling with drywall compound.
Altemativel;y, the web of glass fibers 10 can be saturated and dried with the re-wettable coating 14, then within the same coating line, passed over a kiss coater that applies the desired amount of latex pressure-sensitive adhesive to the fabric. The fabric then passes into a mechanical convection oven for drying of the pressure-sensitive adhesive. In either case, the web 10 is then wound into large diameter rolls for transport to a slitting department where the roll can be processed into tapes of any desired length and width.
PI111$97635. t [0035] In still another variation of the manufacturing method, large rolls of glass; or other fibrous fabric which have been saturated with the re-wettable coating 14 can then be taken to a separate machine called a hot-melt adhesive coater. The pressure-sensitive adhesive can be based on one of a number of hot-melt polymer technologies (su<;h as those described above) rather than latex technology. The hot-melt coater applies; a thin film of molten adhesive to one side of the fabric. The fabric is then formed onto a large roll for transport to the slitting area where it is processed into tapes of any desired length or width. The pressure sensitive adhesive performs the same function whether it is based on hot-melt or latex technology. Only the method of applying the adhesive differs in these two systems.
[0036] The large rolls produced in accordance with the above processes can be processed on slitter/rewinder machines for conversion into tape. The tapes may be of any ,geometry although most are approximately 50mm wide by about 90m long. The tapes are subsequently wrapped, packaged and sent to customers.
Examples [0037] Tensile testing in accordance with ASTM C 474 (appendix) was conducted on assemblies of joint compound and the joint tape, employing the Formulations 1 and 2, to leno weave (46.3 grams/mz), plain weave (47.5 grams/m2) and knit fabric (52.9 grams/m2). These were compared to control samples with SBR coating and a paper tape.
Each tape sample was applied at the butt joint of two sanded polyethylene substrates.
Joint compound is applied in two coats, and allowed to dry for a specif ed time. A
conductive silver paint was applied to the testing area and connected in a series to form a circuit. The sample is then tested under tensile load on a tensile testing machine. When a crack appeared, the circuit failed, and the load is noted.
PH1~$97635.1 [0038] Tensile testing results revealed that the load to first crack could be significantly increased when the re-wettable coating of this invention is used on a glass tape instead of an SBR rubber based coating.
[0039] The data for the average load to first crack (KN) is located below in Table 1.
Table 1: Average Load to First Crack (I~
(appendix)*
GLASS WEB COATING AVG. STANDARD % STANDARD % INCREASE
TYPE FORMULATION DEVIATION DEVIATION
leno weave 1 0.995350.06660 6.69117 56.4 leno weave 2 1.048330.05500 5.24635 64.7 knit fabric 1 1.145330.04948 4.31990 33.8 knit fabric 2 1.169880.07084 6.05531 36.6'!
plain weave 1 1.1815 0.11113 9.40573 15.83 plain weave 2 1.303830.04717 3.61752 27.8 light plain 2 0.9719 0.03865 3.97723 52 weave control lightSBR 0.639470.02935 4.59053 plain weave control wovenSBR 0.636430.10435 16.39574 leno control plainSBR 1.020070.02424 2.37607 weave paper tape NIA 0.577790.06135 10.61801 control control knit SBR 0.855980.03834 4.47865 fabric * Current testing method allows samples to bend out of testing plane when test is in progress.
Thus, 1 S' crack numbers may be false indication of tensile strength. Actual force at 1 s' crack may be higher when no bending or flexing occurs to initiate cracking.
PN 1 v897635. t 5 [0040] This data is reflected in the bar chant of Fig. 4, using averages for Formulations 1 and 2 load reading when available. It was observed in these tests that there was at least about a 16% increase in average load to first crack using the rewettable coating of Formulations 1 and 2 over SBR coatings. Note that all samples were coated on one side with a pressure sensitive adhesive. It would be expected that the average load to first 10 crack would be increased by a factor of two when no adhesive is applied to the back of equivalent samples. The explanation for this is that, in the case of the adhesive coated samples, half of the surface area of the glass web would be covered with a layer of low modulus pressure-sensitive material that does little to resist the loads placed on the sample.
fabric (40%) and lastly, plain weaves (16 to 28%). When tapes without an adhesive backing are tested in accordance with ASTM C474, a similar percent increase in tensile load to failure can be attributed to the invention. However, the magnitude of the results will be about double that of the tapes that are adhesive backed. The explanation for this is that, in the case of the adhesive coated samples, half of the surface area of the glass web IO would be covered with a layer of low modulus pressure-sensitive material that does little to resist tensile loads placed on the sample.
[OOI 1] While standard glass tape products typically fail due to the fiber pulling out from the joint compound, the drywall tape of this invention with the re-wettable coating has been shown to fail by delamination within the joint compound itself. Along with the increased load to tensile failure, delamination in the joint compound suggests that the bond between the coating and the compound is improved since the fibers in the sample do not pull out. The drywall tape of this invention also produces tensile strength results which are approximately twice those previously measured for paper tape, without adding anymore basis weight or fibers to the glass fabric, over that for a conventional glass tape, such as Fibatape~ tape.
[0012] In further embodiments of this invention, the re-wettable coating comprises a soluble or dispersible resinous binder alone, or in combination with a blocking agent, such as a wax. A combination of a soluble binder, such as polyvinyl acetate (PVAc), and wax, offers a strong bond with the joint compound, while also minimizing "blocking" in the tape. The preferred re-wettable coating contains PVAc resin which is very hydroscopic. Water vapor absorption can cause a roll of tape made with PVAc resin to block or fuse together, which causes the roll to bind. The roll of tape can also flow plastically and deform the shape of the tape roll. Blocking agents, such as paravffin wax, make the PVAc-based coating vapor resistant. Only when contacted with liquid water, PH 1 X897635. I
5 such as when the tape is applied to a wall and coated with joint compound, does the PVAc resin re-wet and become soluble.
[0013] In a further embodiment of this invention, a method is provided for preparing a drywall joint. The method includes disposing a pair of drywall boards in adjoining relationship to one another to form a seam region. Next, the drywall tape of this invention is disposed over the seam. This drywall tape includes a web of glass fibers having disposed thereon a resinous binder capable of re-wetting and setting when contacted with the joint compound. A first joint compound layer is applied over the drywall tape so as to re-wet the resinous binder. The first joint compound layer ;and re-wetted resinous binder on the tape are then dried to form an adhesive bond.
Brief Description of the Drawings [0014] The accompanying drawings illustrate preferred embodiments of the invention according to the practical application of the principles thereof, and in which:
[0015] FIG. 1: is a partial, front perspective view of the preferred drywall tape of this invention;
[0016] FIG. 2: is a partial, enlarged side-plan view, illustrating a coating on the drywall tape of FIG. 1;
[0017] FIG. 3: is a partial, top, cross-sectional view of a finished flat drywall joint of this invention; and [0018] FIG. 4: is a graphical depiction of the average load to first crack for various drywall tape constructions, including those of the present invention.
Detailed Description of the Invention [0019) This invention provides drywall tape, drywall joints, methods of preparing drywall joints, and reinforcements for cementitious materials generally. It is understood that PH 11897635. I
while the present invention is preferably related to drywall seam or repair constructions, the re-wettable coatings on the glass and other reinforcing fibrous webs provide practical solutions to reinforcing gypsum fiber board, gypsum wall board, glass-faced gypsum board, tilebacker boards, high impact gypsum wall board, and concrete board constructions. The re-wettable coatings of this invention can be useful with cementitious materials such as gypsum, portland cement, and combinations of these materials with fillers or aggregate, such as mortar, cement and concrete. This invention can be used to enhance the performance of existing self adhesive drywall joint tapes and patches, or tapes and patches which do not have a pressure-sensitive adhesive on one side of their construction. The benefits of a re-wettable resinous binder are realized whether a pressure-sensitive adhesive is present on the web or not. As used herein, the team "drywall" includes wall board, fiberboard, glass-faced gypsum boards, and their-equivalents. As used herein, the term "tape" means a strip of material that can be provided in roll form, which may, or may not, contain an adhesive backing layer.
[0020] With regard to the figures, and particularly to FIGS. 1-2 thereof, there is shown a preferred drywall tape 100 including a web of glass fibers 10 and an optional pressure-sensitive adhesive layer 12. When a portion of the drywall tape 100 is magnified, as shown in FIG. 2, the re-wettable coating 14 can be viewed. In the preferred embodiment of the drywall tape 100, the re-wettable coating 14 is disposed along one or bath sides of the web of glass fibers 10. Alternatively, the re=wettable coating 14 can be di;;posed over 100% of the exterior surfaces of the web of glass fibers 10, over 70% of the surface area, or over less than SO% of the surface area. In certain constructions, the glass fibers of the web of glass fibers 10 are bonded together using a web adhesive binder 15, such as vinyl acetate acrylic, styrene/acrylate, vinyUacetate, acrylic, styrene acrylic, or copolymers and mixtures thereof, ete. In instances where a web adhesive binder 15 is employed, it may or may not be re-wettable, soluble or dispersible in liquid water. In the preferred PH 11897635.1 embodiment, the re-wettable coating 14 is used to also bind the fibers of the web of glass fibers together.
[0021] As shown in FIG. 3, a flat drywall joint can be constructed by butt joining a pair of drywall boards 18 and 17 to form a seam region 45. The drywall tape 100 can be applied with the aid of the pressure-sensitive adhesive Iayer 12, or when a pressure-sensitive adhesive is not employed, the drywall tape 100 can be pressed lightly into a wet joint compound layer which is thinly applied to the seam region 45 prior to application of the drywall tape 100. If joint compound is used to adhere the drywall tape 100 to the seam region 45, care must be taken to provide sufficient joint compound under t)he tape to prevent blistering of the tape. While embedding the tape 100, excess joint compound should be removed from the edge.
(0022] Whether the tape 100 is applied with joint compound, or self-adhered, a first coat of joint compound 30 should applied over the tape so as to embed the tape 100 nearly completely. While embedding the tape 100, excess joint compound is removed from the edge. Added water can be included in the joint compound so as to thin it for ea:~ier application. Similar approaches can be provided for inside corners, outside corners, horizontal flat joints and hole and crack repairs, finished seams along electrical boxes and switches and seams around piping and duct work.
[0023] After the first coat 30 is allowed to dry, preferably overnight, a second coat 40 of drywall compound is applied over the first coat 30, ideally with an 8 inch knife., feathering slightly beyond the first coat. If further coats are desired, the second coat 40 is allowed to dry, and a third or finishing coat (not shown) can be applied with a 1.0 inch knife to the flat joints. The second coat 40 or third coat can be lightly sanded if necessary.
[0024] The joint compound useful in the drywall joints of this invention is typically classified as either a "drying" or "setting" type. In a drying-type joint compound, the PH 0897635.1 S filler comprises substantially calcium carbonate. Prior to use, the filler and the binder, along with several other known ingredients, are mixed with water. After application, when the water drys to evaporation, a dry, relatively hard cementitious material is left behind.
[0025] Joint compositions known as the "setting" type include at least a substantial portion of calcium sulfate hemihydrate. In order to produce calcined gypsum, one converts calcium sulfate dihydrate from raw gypsum to the hemihydrate state through a known process called calcination. This process removes 1 ~h molecules of water from the calcium sulfate dihydrate gypsum. The hemihydrate form of calcium sulfate is substantially more soluble in water than the dihydxate form of calcium sulfate. wring 1S use of a setting-type joint compound, the calcium sulfate hemihydrate is rehydrated to the dihydrate state. This rehydration process normally takes place over a fairly short period of time. Accordingly, it is extremely difficult to produce a setting-type joint compound for storage in a bucket, and as such, such compounds are typically provided in powder form. Setting-type joint compounds also form a crystalline network upon setting, and provide a stronger, more durable bond.
[0026] The webs useful in manufacturing the drywall tape I00 of this invention can be provided as non-woven, woven or knitted fabrics, veils, mats, scrims, or fleece. They desirably include high strength fibers, such as glass fiber, and less desirably may include thermoplastic or thermosetting fibers, carbon, boron, graphite fibers or combinations 2S thereof. In most examples of this invention, a web of glass fibers 10 having a basis weight of about S-500 grams/m', preferably about 20-120 grams/m2, is employed.
This web 10 can be fabricated by weaving, such as a plane or leno weave, by knitting, by a laid scrim process or by a non-woven process, such as resin bonding randomly oriented glass fibers. The webs of this invention are, desirably, at least partially porous to wca joint compound so as to form a good bond in the seam region 4S. Alternatively, a veil or PH 11897635.1 fabric could be somewhat non-porous to joint compound and still be useful as a replacement for paper tape and, thus, be applied with a bedding coat of joint compound.
[0027] The preferred re-wettable coating 14 applied to the web desirably has the properties of being soluble or dispersible in liquid water. Glass tapes of the past were often coated with polymers, such as SBR rubber or a resinous binder, such as virnyl acetate acrylic, styrene/acrylate, vinyUacetate, acrylic, styrene acrylic, etc., which wee specifically designed to aid in handling and slitting the reinforcements without regard to how the coatings interacted with joint compounds. The adhesion of traditional rubber based coatings such as SBR to setting or non-setting joint compounds is minimal, and thus, an optimum composite strength cannot be achieved, e.g., the glass fibers tend to pull out from compound when loaded. The preferred re-wettable coatings 14 of this invention set to form a strong bond between the preferred glass fibers and the set joint compound so that the fibers act more as an unit to resist loads. The preferred re-wettable coating 14 of this invention should be as inexpensive as the styrene butadiene rubber (SBR) or joining resin binders currently employed on glass drywall tape. This coating 14 should be easy and versatile to formulate and should run on pad rolls with water clean up being; highly desirable. It should not be significantly prone to oxidation or W light degradation.
Ideally, the preferred re-wettable coating 14 i.s provided in a latex form such as an aqueous emulsion of a binder resin, blocking agent and water.
[0028] The preferred re-wettable coating 14 of this invention contains one or more of the resins selected from the group including: polyvinyl acetate, ethylene vinyl acetate, polystyrene, polyvinyl chloride, polyacrylate, ethylene acetate co-polymer, vinyl-acrylic co-polymer, styrene butadiene, acrylic polymer and starch; protein glues, such as casein, soy protein, animal glue and gelatin; vegetable-based glues, such as cellulosics and their chemically modified derivatives; gums (polysaccharides and carbohydrates) such as guar gum; resins (pine tar) which may not be water soluble; mucilages (agar, carrageenan and PH 1897635.1 5 algin); inorganics such as soluble silicates (water glass) and cementitious materi<ils (cement, gypsum), and co-polymers and combinations of these. Most preferably, the resinous binder contains polyvinyl acetate (PVAc), such as Vinac 524 polyvinyl acetate homopolymer stabilized with polyvinyl alcohol, Airflex 401 polyvinyl acetateJethylene co-polymer stabilized with polyvinyl alcohol, both supplied by Air Products and 10 Chemicals, Inc., of 7201 Hamilton Blvd., Allentown, PA 18195. The re-wettable coating 14 preferably is provided in an aqueous emulsion or solution containing about 2.5-75 wt.
% solids. Alternatively, water soluble polymers in powder form may be applied with adhesive or electrostatically. Two formulations of the re-wettable coating developed within the context of this invention are found below:
(0029] Formulation 1 Vinac 524 Emulsion (PVAc homopolymer stabilized with polyvinyl alcohol) 61.38%
Airflex 40I Emulsion (PVAc/ethylene co-polymer stabilized with polyvinyl alcohol 26.30'%
Water 9.02%
Urea 0.25%
Hydrocer DP69 (paraffin wax, anti-blocking agent) 3.00%
900-103 Henkel Foamaster NXZ mixed 50/50% with water. 0.05%
Other pertinent formula data:
Solids level: 50%
Viscosity: about 1000 cps PH: approximately 6.0 f'H 11897635.1 S [0030] Formulation 2 Vinac S24 Emulsion (PVAc homopolymer 74.53%
stabilized with polyvinyl alcohol) Benzoflex 9-88 (dipropylene glycol dibenzoate plasticizer for PVAc) 7.23%
Urea 0.25%
Hydrocer DP69 (paraffin wax, anti-blocking agent) 3.00%~
Water 14.94°!~
900-103 Henkel Foamaster NXZ mixed SO/SO% with water O.OS%~
(0031] As reflected above, an important ingredient for preventing the PVAc resin from picking up too much water during storage is an anti-blocking agent, such as animal oils, fats, starch, dextrine, silicone oil, waxes and combinations thereof. The preferred anti-blocking agent is low melting point paraffin wax. The paraffin wax can be emulsified in the formulations and "blooms" to the surface when the formation is dried. The blocking agent acts as a vapor burner to the re-wettable 14 coating on the drywall tape 100 of this invention, so as to substantially reduce blocking in tape rolls. The anti-blocking agent should be less than about S-10% by weight of the formulation so that it can be dispersed readily when the re-wettable coating 14 is made soluble by the water in the joint compound. Accordingly, the re-wettable coating 14 with the above formulations containing an anti-blocking agent and PVAc resin in solution, is capable of being vapor resistant when dry, but is water soluble or dispersible when contacted with liquid water in the joint compound.
[0032] The adhesive elements of this invention can be made of any known pressure-sensitive adhesive material. As used herein, the term "pressure-sensitive"
refers to any releasable adhesive or releasable tenacious means. Adhesive compositions suitable for tape include, for example, the water-based pressure-sensitive adhesive such as acrylate adhesives, e.g., isooctyl acrylate and acrylic acid copolymer, or vinyl acetate-2 ethyl hexyl acrylate copolymer which can be combined with tackifiers. Alternatively, the adhesive PHl897635.t may comprise the rapid setting thermoplastic "hot melt" adhesives. The adhesive elements may also comprise a two-sided adhesive tape. It is also anticipated that.
adhesives based on an elastomer selected from natural or synthetic rubbers could be used.
It will be understood that alternative shapes for these adhesives, for examples, continuous coatings, discontinuous lines, squares, dots, circles, etc., may be employed.
IO [0033] The preferred method of manufacturing the drywall tape I00 of this invention shall now be described. The glass fabric knitted web of 42.1 - 52.9 grams/m2 is first passed through a bath of latex including the Formulations 1 or 2 and then through a set of squeeze rollers, which sen~e to control the amount of latex picked up by the fab>-ic, usually about 5-20 grams/m2 of coating when dry. The rollers could be adjusted for gap width or pressure to perform this function, but the solids level and the viscosity of the latex are important factors in determining the coating weight. The saturated fabric is then dried either by contact with steam cans or by convection in a hot oven.
[0034] At this point, the web of glass fibers 10, now coated with a re-wettable coating I4, is provided with a pressure sensitive adhesive layer 12 applied to one side, usually about 3-15 grams/m' of adhesive is applied. This may be done in a subsequent step on a separate finishing machine, or directly in line with the re-wettable coating step. The pressure-sensitive adhesive layer 12 serves to affix the drywall tape 100 to the drywall surface in preparation for drywall filling with drywall compound.
Altemativel;y, the web of glass fibers 10 can be saturated and dried with the re-wettable coating 14, then within the same coating line, passed over a kiss coater that applies the desired amount of latex pressure-sensitive adhesive to the fabric. The fabric then passes into a mechanical convection oven for drying of the pressure-sensitive adhesive. In either case, the web 10 is then wound into large diameter rolls for transport to a slitting department where the roll can be processed into tapes of any desired length and width.
PI111$97635. t [0035] In still another variation of the manufacturing method, large rolls of glass; or other fibrous fabric which have been saturated with the re-wettable coating 14 can then be taken to a separate machine called a hot-melt adhesive coater. The pressure-sensitive adhesive can be based on one of a number of hot-melt polymer technologies (su<;h as those described above) rather than latex technology. The hot-melt coater applies; a thin film of molten adhesive to one side of the fabric. The fabric is then formed onto a large roll for transport to the slitting area where it is processed into tapes of any desired length or width. The pressure sensitive adhesive performs the same function whether it is based on hot-melt or latex technology. Only the method of applying the adhesive differs in these two systems.
[0036] The large rolls produced in accordance with the above processes can be processed on slitter/rewinder machines for conversion into tape. The tapes may be of any ,geometry although most are approximately 50mm wide by about 90m long. The tapes are subsequently wrapped, packaged and sent to customers.
Examples [0037] Tensile testing in accordance with ASTM C 474 (appendix) was conducted on assemblies of joint compound and the joint tape, employing the Formulations 1 and 2, to leno weave (46.3 grams/mz), plain weave (47.5 grams/m2) and knit fabric (52.9 grams/m2). These were compared to control samples with SBR coating and a paper tape.
Each tape sample was applied at the butt joint of two sanded polyethylene substrates.
Joint compound is applied in two coats, and allowed to dry for a specif ed time. A
conductive silver paint was applied to the testing area and connected in a series to form a circuit. The sample is then tested under tensile load on a tensile testing machine. When a crack appeared, the circuit failed, and the load is noted.
PH1~$97635.1 [0038] Tensile testing results revealed that the load to first crack could be significantly increased when the re-wettable coating of this invention is used on a glass tape instead of an SBR rubber based coating.
[0039] The data for the average load to first crack (KN) is located below in Table 1.
Table 1: Average Load to First Crack (I~
(appendix)*
GLASS WEB COATING AVG. STANDARD % STANDARD % INCREASE
TYPE FORMULATION DEVIATION DEVIATION
leno weave 1 0.995350.06660 6.69117 56.4 leno weave 2 1.048330.05500 5.24635 64.7 knit fabric 1 1.145330.04948 4.31990 33.8 knit fabric 2 1.169880.07084 6.05531 36.6'!
plain weave 1 1.1815 0.11113 9.40573 15.83 plain weave 2 1.303830.04717 3.61752 27.8 light plain 2 0.9719 0.03865 3.97723 52 weave control lightSBR 0.639470.02935 4.59053 plain weave control wovenSBR 0.636430.10435 16.39574 leno control plainSBR 1.020070.02424 2.37607 weave paper tape NIA 0.577790.06135 10.61801 control control knit SBR 0.855980.03834 4.47865 fabric * Current testing method allows samples to bend out of testing plane when test is in progress.
Thus, 1 S' crack numbers may be false indication of tensile strength. Actual force at 1 s' crack may be higher when no bending or flexing occurs to initiate cracking.
PN 1 v897635. t 5 [0040] This data is reflected in the bar chant of Fig. 4, using averages for Formulations 1 and 2 load reading when available. It was observed in these tests that there was at least about a 16% increase in average load to first crack using the rewettable coating of Formulations 1 and 2 over SBR coatings. Note that all samples were coated on one side with a pressure sensitive adhesive. It would be expected that the average load to first 10 crack would be increased by a factor of two when no adhesive is applied to the back of equivalent samples. The explanation for this is that, in the case of the adhesive coated samples, half of the surface area of the glass web would be covered with a layer of low modulus pressure-sensitive material that does little to resist the loads placed on the sample.
15 [0041] It was additionally observed that, while standard products fail by fiber pull-out from the joint compound, the re-wettable coatings of this invention failed by delamination of the joint compound proximate to the coated fiber. Although the tensile test is conducted on polyethylene blocks, where it is expected that the adhesion of the joint compound to the polyethylene would be poor, real drywall testing may demonstrate even better results.
[0042] From the foregoing it can be realized that this invention provides drywall joints and methods of joint fabrication which demonstrate improved tensile properties over kraft tape joints and over other glass tape joints employing rubber based or binder coatings.
The tape constructions of this invention employ a re-wettable coating containing in the preferred embodiment a resinous binder which is at least partially soluble or dispersible in the aqueous mixture of most joint compounds. Although various embodiments have been illustrated, this was for the purpose of describing, but not limiting the invention. Various modifications, which will become apparent to one skilled in the art, are within the scope of this invention described in the attached claims.
PH 1897635.1
[0042] From the foregoing it can be realized that this invention provides drywall joints and methods of joint fabrication which demonstrate improved tensile properties over kraft tape joints and over other glass tape joints employing rubber based or binder coatings.
The tape constructions of this invention employ a re-wettable coating containing in the preferred embodiment a resinous binder which is at least partially soluble or dispersible in the aqueous mixture of most joint compounds. Although various embodiments have been illustrated, this was for the purpose of describing, but not limiting the invention. Various modifications, which will become apparent to one skilled in the art, are within the scope of this invention described in the attached claims.
PH 1897635.1
Claims (23)
1. A drywall tape suitable for joint compound repairs and joint covering, comprising:
a web of glass fibers; and a coating disposed over a portion of said glass fibers in said web, said coating comprising a resinous binder being at least partially soluble or dispersible in said joint compound, and capable of forming an adhesive bond with said joint compound when sets.
a web of glass fibers; and a coating disposed over a portion of said glass fibers in said web, said coating comprising a resinous binder being at least partially soluble or dispersible in said joint compound, and capable of forming an adhesive bond with said joint compound when sets.
2. The drywall tape of claim 1 wherein said web comprises a non-woven fabric, woven fabric, knitted fabric, mat or scrim.
3. The drywall tape of claim 1 wherein said resinous binder comprises an aqueous emulsion or solution applied to said portion of glass fibers and then dried to form said coating.
4. The drywall tape of claim 3 wherein said aqueous emulsion or solution comprises one or more resins selected from the group comprising: polyvinyl alcohol, polyvinyl acetate, polystyrene, polyvinylchloride, polyacrylate, ethylene vinyl acetate co-polymer, vinyl-acrylic co-polymer, styrene butadiene, acrylic polymer, starch, protein glues, soy protein, animal glue, gelatin, vegetable-based glue, gum, resin, mucilage, inorganic compound, cementitious material and copolymers and combinations thereof.
5. The drywall tape of claim 1 wherein said joint compound comprises an acrylic polymer and said resinous binder comprises polyvinyl alcohol, vinyl-acrylic co-polymer, polyvinyl acetate, or a combination thereof.
6. The drywall tape of claim 1 wherein said web further comprises a pressure sensitive adhesive disposed on a first surface thereof.
7. The drywall tape of claim 6 wherein said coated web is slit and wound into a roll of tape.
8. The drywall tape of claim 1 wherein said resinous binder is applied as an aqueous emulsion having at least about 25-75 wt. % solids.
9. The drywall tape of claim 1 wherein said resinous binder comprises an aqueous emulsion of polyvinyl acetate applied to said web and dried to form said coating.
10. The drywall tape of claim 1, further comprising an anti-blocking agent.
11. The drywall tape of claim 10, wherein said anti-blocking agent comprises less than about wt. % of a waxy substance.
12 A drywall joint comprising:
a pair of drywall boards adjoined to form a seam region;
a drywall tape disposed over a portion of said seam region, said drywall tape comprising a web of glass fibers and a coating disposed thereon, said coating comprising a resinous binder capable of re-wetting when contacted by liquid water;
a first joint compound layer containing liquid water in solution disposed over said drywall tape, said liquid water of said first joint compound layer re-wetting the resinous binder in said coating, said first joint compound layer and said re-wetted coating drying to form an adhesive bond; and a second joint compound layer disposed over said first joint compound layer.
a pair of drywall boards adjoined to form a seam region;
a drywall tape disposed over a portion of said seam region, said drywall tape comprising a web of glass fibers and a coating disposed thereon, said coating comprising a resinous binder capable of re-wetting when contacted by liquid water;
a first joint compound layer containing liquid water in solution disposed over said drywall tape, said liquid water of said first joint compound layer re-wetting the resinous binder in said coating, said first joint compound layer and said re-wetted coating drying to form an adhesive bond; and a second joint compound layer disposed over said first joint compound layer.
13. The drywall joint of claim 12 wherein said resinous coating comprises one or more of the group selected from: polyvinyl alcohol, polyvinyl acetate, polystyrene, polyvinylchloride, polyacrylate, ethylene vinyl acetate co-polymer, vinyl-acrylic co-polymer, styrene butadiene, acrylic polymer, starch, protein glues, soy protein, animal glue, gelatin, vegetable-based glue, gum, resin, mucilage, inorganic compound, cementitious material and copolymers and combinations thereof.
14. The drywall joint of claim 12 wherein said web of glass fibers comprises a non-woven fabric, woven fabric, knitted fabric, mat or scrim.
15. The drywall joint of claim 12 wherein said web comprises a pressure sensitive adhesive disposed on a first surface thereof, said pressure sensitive adhesive adhering said web of glass fibers to said seam region.
16. The drywall joint of claim 12 wherein said resinous coating comprises is a water vapor resistant composition compromising PVAc and an anti-blocking agent.
17. The drywall joint of claim 16 wherein said anti-blocking agent comprises a waxy substance.
18. The drywall joint of claim 12 wherein said adhesive bond between said first joint compound layer and said coating is stronger than the tensile strength of the set compound of said first joint compound layer.
19 19. A method of preparing a drywall joint comprising:
disposing a pair of drywall boards in adjoining relationship to one another to form a seam region;
disposing a drywall tape over said seam region, said drywall tape comprising a web of glass fibers having disposed thereon a resinous binder capable of re-wetting and setting when contacted with a joint compound to form an adhesive bond therewith;
applying a first joint compound layer over said drywall tape whereby a portion of said resinous binder is re-wetted; and drying said first joint compound layer and said re-wetted resinous binder together to form an adhesive bond.
disposing a pair of drywall boards in adjoining relationship to one another to form a seam region;
disposing a drywall tape over said seam region, said drywall tape comprising a web of glass fibers having disposed thereon a resinous binder capable of re-wetting and setting when contacted with a joint compound to form an adhesive bond therewith;
applying a first joint compound layer over said drywall tape whereby a portion of said resinous binder is re-wetted; and drying said first joint compound layer and said re-wetted resinous binder together to form an adhesive bond.
20. The method of claim 19 wherein said finished drywall joint has an average load to first crack ASTM C 474 (Appendix) which is at least 16% greater than a similarly prepared finished drywall joint without said resinous binder.
21. The method of claim 19 wherein said drywall tape is adhered to said drywall seam region by a pressure sensitive adhesive.
22. A finished drywall seam or repair region, comprising:
a drywall seam or repair region;
a drywall tape comprising a web of glass fibers, including a re-wettable, resinous coating disposed at least on a first surface of said web, and a pressure-sensitive adhesive disposed on at least a second surface of said web;
said drywall tape adhered to the seam or repair region by said pressure-sensitive adhesive so as to substantially cover said seam or repair region;
a first joint compound layer containing liquid water in solution disposed over said drywall tape, wherein said liquid water re-wets the re-wettable, resinous binder, said first joint compound layer and said re-wetted, resinous binder drying to form an adhesive bond joining said web to said first joint compound layer;
said finished drywall joint comprising at least a 16% improvement in the:
average load to first crack under tensile load ASTM C474 (Appendix) over a similarly prepared finished drywall joint which does not contain said re-wettable resinous binder.
a drywall seam or repair region;
a drywall tape comprising a web of glass fibers, including a re-wettable, resinous coating disposed at least on a first surface of said web, and a pressure-sensitive adhesive disposed on at least a second surface of said web;
said drywall tape adhered to the seam or repair region by said pressure-sensitive adhesive so as to substantially cover said seam or repair region;
a first joint compound layer containing liquid water in solution disposed over said drywall tape, wherein said liquid water re-wets the re-wettable, resinous binder, said first joint compound layer and said re-wetted, resinous binder drying to form an adhesive bond joining said web to said first joint compound layer;
said finished drywall joint comprising at least a 16% improvement in the:
average load to first crack under tensile load ASTM C474 (Appendix) over a similarly prepared finished drywall joint which does not contain said re-wettable resinous binder.
23. The finished drywall seam or repair region of claim 22, wherein said re-wettable resinous coating comprises a dried emulsion including wax and polyvinyl acetate.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PCT/IB2003/002226 WO2004099529A1 (en) | 2003-05-06 | 2003-05-06 | Drywall tape and joint |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2427514A1 true CA2427514A1 (en) | 2004-11-01 |
Family
ID=34385732
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002427514A Abandoned CA2427514A1 (en) | 2003-05-06 | 2003-05-01 | Drywall tape and joint |
| CA002525971A Expired - Lifetime CA2525971C (en) | 2003-05-06 | 2003-05-06 | Drywall tape and joint |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002525971A Expired - Lifetime CA2525971C (en) | 2003-05-06 | 2003-05-06 | Drywall tape and joint |
Country Status (7)
| Country | Link |
|---|---|
| EP (1) | EP1620613A1 (en) |
| JP (1) | JP2007516366A (en) |
| CN (1) | CN1788130A (en) |
| AU (1) | AU2003232993A1 (en) |
| BR (1) | BR0318297A (en) |
| CA (2) | CA2427514A1 (en) |
| WO (1) | WO2004099529A1 (en) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20080118728A1 (en) | 2006-10-20 | 2008-05-22 | Dow Global Technologies Inc. | Aqueous dispersions disposed on glass-based fibers and glass-containing substrates |
| US9376824B2 (en) * | 2006-12-12 | 2016-06-28 | United States Gypsum Company | Nonwoven joint tape having low moisture expansion properties and method for using same |
| US8828892B2 (en) | 2007-01-18 | 2014-09-09 | Saint-Gobain Adfors Canada, Ltd. | Drywall tape and drywall joint |
| AU2010220805A1 (en) * | 2009-03-05 | 2011-10-20 | Csr Building Products Limited | Improved plasterboard jointing system |
| FR2953531B1 (en) | 2009-12-07 | 2012-03-02 | Ahlstroem Oy | NON-WOVEN SUPPORT FOR JOINT STRIP AND STABLE, DIMENSIONALLY STABLE SEALING STRIP WITHOUT LOSS OF MECHANICAL STRENGTH COMPRISING SAID SUPPORT |
| AR093506A1 (en) * | 2012-11-16 | 2015-06-10 | Shawcor Ltd | REINFORCED TAPE OR SHEET WITH FIBERS FOR REINFORCING PIPES |
| CN103643516B (en) * | 2013-12-02 | 2016-01-20 | 山东永泰化工有限公司 | A kind of preparation method of glass fibre wallhanging coating |
| US11066576B2 (en) * | 2015-09-21 | 2021-07-20 | United States Gypsum Company | Drywall joint tape with dual purpose adhesive backing |
| CN107905407A (en) * | 2017-12-01 | 2018-04-13 | 中冶天工集团天津有限公司 | A method for anti-seismic and anti-cracking of fireproof gypsum wallboard joints |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3391037A (en) * | 1964-10-12 | 1968-07-02 | Joseph D. Mcnulty | Method of covering joints in interior wall construction |
| CA957120A (en) * | 1971-01-28 | 1974-11-05 | Joseph W. Schneller | Drywall joint system |
-
2003
- 2003-05-01 CA CA002427514A patent/CA2427514A1/en not_active Abandoned
- 2003-05-06 CA CA002525971A patent/CA2525971C/en not_active Expired - Lifetime
- 2003-05-06 JP JP2004571534A patent/JP2007516366A/en active Pending
- 2003-05-06 WO PCT/IB2003/002226 patent/WO2004099529A1/en not_active Ceased
- 2003-05-06 BR BRPI0318297-5A patent/BR0318297A/en not_active IP Right Cessation
- 2003-05-06 EP EP03727793A patent/EP1620613A1/en not_active Withdrawn
- 2003-05-06 AU AU2003232993A patent/AU2003232993A1/en not_active Abandoned
- 2003-05-06 CN CNA038265796A patent/CN1788130A/en active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| CA2525971A1 (en) | 2004-11-18 |
| BR0318297A (en) | 2006-07-11 |
| AU2003232993A1 (en) | 2004-11-26 |
| WO2004099529A1 (en) | 2004-11-18 |
| AU2003232993A8 (en) | 2004-11-26 |
| CA2525971C (en) | 2008-11-18 |
| EP1620613A1 (en) | 2006-02-01 |
| JP2007516366A (en) | 2007-06-21 |
| CN1788130A (en) | 2006-06-14 |
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