IP Library Granted Patent US 12,503,620
Granted Patent B2
US 12,503,620 · App. 17/311,086 · Granted Dec 23, 2025

Thin layer UV curing coating on non-woven facers

Inventors: Xin Wang (Fort Mill, SC); Paul Geel (Heveadorp, NL)
Assignee: Owens Corning Intellectual Capital, LLC
C09D163/10C09D4/00C09D183/10D06N3/0011D06N3/042D06N2211/06
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Quick Facts
Patent No.
US 12,503,620
App. No.
17/311,086
Granted
Dec 23, 2025
Kind
B2
Abstract

A UV-cured coated facer includes a non-woven mat having a first side and a second side and an intermediate coating disposed on the first side of the non-woven mat. The intermediate coating includes a coating binder and a filler. The UV-cured coated facer also includes a UV-curable coating composition disposed on the intermediate coating, wherein the UV-curable coating composition is essentially free of a filler.

Claims (26)

1 . A UV-cured coated facer comprising:

a non-woven mat having a first side and a second side;

50 g/m 2 to 300 g/m 2 of a cured intermediate coating disposed on the first side of the non-woven mat; wherein the cured intermediate coating comprises 5.5 to 20 weight percent of a coating binder and at least 75 weight percent of a filler, wherein the coating binder comprises a water-based polymer emulsion or solution; and

a UV-cured coating composition disposed on the cured intermediate coating, wherein said UV-cured coating composition is essentially free of a filler, wherein the UV-cured coating composition comprises the reaction product of at least one polyfunctional oligomer, at least one reactive diluent, and at least one photoinitiator blend comprising a Type II photoinitiator and an amine, and is applied to the intermediate layer with a thickness of 5 μm to 100 μm;

wherein the UV-cured coated facer has a Gurley air permeation number from 50,000 s to 150,000 s.

2 . The UV-cured coated facer of claim 1 , where the UV-cured coated facer has a percent weight loss that is 50% less than a facer with a comparable filled coating when an abrasion test is performed by cycling a wire bristle brush head on the facer for 50 cycles.

3 . The UV-cured coated facer of claim 1 , wherein the UV-cured coating composition has a solids content with a weight percent greater than 90%.

4 . The UV-cured coated facer of claim 1 , where the reactive diluent is selected from (meth) acrylates, (meth) acrylic acids, vinyl aromatics, divinyl ethers, and N-vinyl pyrrolidone, and combinations thereof.

5 . The UV-cured coated facer of claim 1 , where the polyfunctional oligomer is selected from epoxy acrylates, urethane acrylates, polyester acrylates, polyether acrylates, soy oil acrylates and straight-chained acrylic oligomers.

6 . The UV-cured coated facer of claim 1 , where the UV-cured coating composition further comprises one or more additives selected from the group consisting of surfactants, UV stabilizers, oxygen inhibitors, and pigments.

7 . A construction board that includes the UV-cured coated facer of claim 1 .

8 . The construction board of claim 7 , wherein the second side of the coated facer is attached to a gypsum board.

9 . The construction board of claim 7 , wherein the second side of the coated facer is attached to a polyisocyanurate board.

10 . A method for preparing a UV-cured coated facer comprising:

providing a non-woven fiber mat;

forming an intermediate coating on the non-woven fiber mat by coating the non-woven fiber mat with 50 g/m 2 to 300 g/m 2 of a coating composition including 5.5 to 20 weight percent of a coating binder and at least 75 weight percent of a filler;

curing the intermediate coating composition on the non-woven fiber mat;

coating the intermediate coating with UV-curable coating composition, wherein the UV-curable coating composition comprises at least one polyfunctional oligomer, at least one reactive diluent, and at least one photoinitiator blend comprising a Type II photoinitiator and an amine, and is essentially free of a filler, wherein the UV-curable coating composition is applied to the intermediate layer at a thickness of 5 μm to 100 μm; and

supplying a UV-light source to cure the UV-curable coating composition, forming a UV-cured coated facer;

wherein the UV-cured coated facer has a Gurley air permeation number from 50,000 s to 150,000 s.

11 . The method of claim 10 , where the UV-curable coating composition has a solids content with a weight percent of at least 90%.

12 . The method of claim 11 , where wherein said UV-curable coating composition has a solids content with a weight percent of at least 99%.

13 . The method of claim 10 , where the reactive diluent is selected from (meth) acrylates, (meth) acrylic acids, vinyl aromatics, divinyl ethers, and N-vinyl pyrrolidone, and combinations thereof.

14 . The method of claim 10 , where the polyfunctional oligomer is selected from epoxy acrylates, urethane acrylates, polyester acrylates, polyether acrylates, soy oil acrylates and straight-chained acrylic oligomers.

15 . The method of claim 10 , where the UV curable coating composition further comprises an additive selected from the group consisting of surfactants, UV stabilizers, oxygen inhibitors, and pigments.

16 . The method of claim 10 , where the non-woven fiber mat is a non-woven glass fiber mat.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 9, 2021
From: WANG, XIN; GEEL, PAUL
To: OCV INTELLECTUAL CAPITAL, LLC
Reel/Frame 056492/0068 →
MERGER Recorded Jun 9, 2021
From: OCV INTELLECTUAL CAPITAL, LLC
To: OWENS CORNING INTELLECTUAL CAPITAL, LLC
Reel/Frame 056492/0076 →
Continuity (2)
Provisional Application 62781770 · Dec 19, 2018
Related Publication 20210332260A1 · Oct 28, 2021
References Cited (22)
US 3842559A · Payne · 1974 [cited by examiner]
US 5288523A · Klaiber et al. · 1994 [cited by applicant]
US 6277939B1 · Smith · 2001 [cited by applicant]
US 6316089B1 · Ohtani et al. · 2001 [cited by applicant]
US 7087696B2 · Wiesendanger et al. · 2006 [cited by applicant]
US 7323248B2 · Ramsey · 2008 [cited by applicant]
US 7553780B2 · Smith · 2009 [cited by applicant]
US 8268737B1 · Kumar · 2012 [cited by applicant]
US 9475967B2 · Lipscomb et al. · 2016 [cited by applicant]
US 9701802B2 · Bushmire et al. · 2017 [cited by applicant]
US 20040170873A1 · Smith · 2004 [cited by examiner]
US 20080124576A1 · Elliott · 2008 [cited by applicant]
US 20170326761A1 · Springer · 2017 [cited by applicant]
CA 2774509A1 · 2013 [cited by applicant]
DE 102017001274A1 · 2018 [cited by applicant]
EP 1801278A1 · 2007 [cited by applicant]
WO 2000014358A2 · 2000 [cited by applicant]
WO 2004055286A2 · 2004 [cited by applicant]
WO 2004094723A1 · 2004 [cited by applicant]
Communication from EP Application No. 19848914.8 dated Jul. 15, 2022. [cited by applicant]
International Search Report and Written Opinion from PCT/US2019/067040 dated Mar. 26, 2020. [cited by applicant]
Office Action from CA Application No. 31,123,938 dated Oct. 22, 2024. [cited by applicant]