IP Library Granted Patent US 12,559,641
Granted Patent B2
US 12,559,641 · App. 16/386,594 · Granted Feb 24, 2026

Printed appliance component

Inventors: Urban Weber (Weiler bei Bingen, DE); Inga Gheczy (Wiesbaden, DE); Jochen Drewke (Mainz, DE); Kevin Duval (Penetanguishene, CA); Lucas Alousis (Riesweiler, CA); Stephanie Mangold (Klein-Winternheim, DE)
Assignee: SCHOTT AG
C09D11/54B32B17/10B41M5/0017B41M5/0047B41M5/007C03C17/30C03C17/32C09D11/037C09D11/102C09D11/107C09D11/108C09D11/322C09D11/38B41M1/34C03C17/34C03C17/3405C03C2217/445C03C2217/485C03C2217/72C03C2218/10C03C2218/112C03C2218/119C09D5/002C09D7/40C09D11/40C09D125/08C09D125/14C09D133/06C09D133/062C09D183/08Y10T428/24901Y10T428/24926
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 12,559,641
App. No.
16/386,594
Granted
Feb 24, 2026
Kind
B2
Abstract

A method for producing an appliance component is provided. The appliance component has an operational front side and back side and has a substrate made of thermally tempered flat glass with a coating. The method includes the steprs of: a) providing a glass substrate made of thermally tempered glass with the dimensions of the appliance component; b) applying a preparation for producing an adhesion promoter layer onto a surface of the glass substrate, wherein the preparation is applied onto the surface of the glass substrate that forms the operational back side of the decorative panel; c) producing the adhesion promoter layer by polymerization of the preparation applied in step b); d) applying a preparation for producing an organic color layer onto the adhesion promoter layer produced in step c) by digital printing; and e) producing the organic color layer by polymerization of the preparation applied in step d).

Claims (22)

1 . An appliance component, comprising:

a glass substrate having an operational front side that faces a user and an operational back side that faces an inside of the appliance, the glass substrate being made of thermally tempered flat glass;

a coating only on the operational back side, wherein the coating comprises at least two coatings, wherein the at least two coatings comprise an intrinsically colored adhesion promoting layer adjacent to the operational back side and an organic color layer applied to the adhesion promoting layer, wherein the organic color layer is a digitally printed layer having a polymer matrix and a colorant;

wherein the adhesion promoting layer comprises a polymer matrix with functional groups for bonding to the glass substrate, and wherein the adhesion promoting layer is between the glass substrate and the organic color layer;

wherein the adhesion promoting layer has a transmittance of at least 80% for a light wavelength range between 380-780 nm at a layer thickness in a range of between 1-5 μm, and wherein the organic color layer is viewable through the adhesion promotor layer and through the glass substrate, from the operational front side of the glass substrate with a mean color coordinate shift ΔE caused by the adhesion promoting layer that is <15 for a color blue, is <5 for a color red, and is <6 for a color green, and

wherein:

(a) the adhesion promoting layer comprises a copolymer containing the following monomer units:

wherein R1 is an aromatic residue, R2 is an aliphatic residue or an aliphatic acid, R3 is hydrogen or a methyl group, and R4 is an aliphatic or aromatic residue;

or

(b) the polymer matrix of the adhesion promoter promoting layer is crosslinked by Si—O—Si bonds and carbon-carbon bonds.

2 . The appliance component of claim 1 , wherein the glass substrate is selected from a group consisting of a substrate having a thickness of at least 2.5 mm, a substrate having a thickness in a range of 3 to 8 mm, and a substrate having a thickness in a range of 3.5 to 5.5 mm.

3 . The appliance component of claim 1 , wherein the polymer matrix of the adhesion promoting layer is formed from monomer units of at least one monomer with radically polymerizable groups.

4 . The appliance component of claim 1 , wherein the polymer matrix of the organic color layer comprises a crosslinked polyacrylic matrix and at least one organic colorant.

5 . The appliance component of claim 1 , wherein the organic color layer comprises at least one light stabilizer comprising a constituent selected from the group consisting of HALS, piperidine derivatives, and organic aromatic compounds with extended π-systems.

6 . The appliance component of claim 1 , wherein the organic color layer is a single layer having a force required for delamination from the glass substrate of 3.5 to 5 N.

7 . The appliance component of claim 1 , wherein the organic color layer comprises two layers and that the coating has a force required for delamination from the glass substrate of 5 to 7 N.

8 . The appliance component of claim 1 , wherein the organic color layer comprises three layers and that the coating has a force required for delamination from the glass substrate of 14 to 16 N.

9 . The appliance component of claim 1 , wherein the coating further comprises an opaque cover layer arranged on the organic color layer.

10 . The appliance component of claim 1 , wherein the glass substrate is a soda-lime glass substrate.

11 . The appliance component of claim 1 , wherein the polymer matrix of the adhesion promoting layer comprises silanes with polymerizable groups, and silsesquioxanes with polymerizable groups.

12 . The appliance component of claim 1 , wherein the polymer matrix of the adhesion promoting layer comprises pre-hydrolysates of silanes with polymerizable groups as monomer units.

13 . The appliance component of claim 1 , wherein the polymer matrix of the adhesion promoting layer comprises trialkoxysilanes containing an acrylic or vinyl group.

Assignments (2)
NUNC PRO TUNC ASSIGNMENT Recorded Dec 17, 2021
From: SCHOTT GEMTRON CORPORATION; SCHOTT AG
To: SCHOTT AG
Reel/Frame 058413/0496 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 2, 2019
From: WEBER, URBAN, DR.; GHECZY, INGA; DREWKE, JOCHEN; DUVAL, KEVIN; ALOUSIS, LUCAS; MANGOLD, STEPHANIE
To: SCHOTT AG; SCHOTT GEMTRON CORPORATION
Reel/Frame 049649/0413 →
Priority Claims (1)
DE 10 2018 109 102.8 · Apr 17, 2018 · national
Continuity (1)
Related Publication 20190315991A1 · Oct 17, 2019
References Cited (54)
US 6136382A · Kamen · 2000 [cited by examiner]
US 10434818B2 · O'Ryan · 2019 [cited by examiner]
US 10933685B2 · O'Ryan · 2021 [cited by examiner]
US 20020128351A1 · Kiguchi · 2002 [cited by examiner]
US 20030021961A1 · Ylitalo · 2003 [cited by examiner]
US 20030069329A1 · Kubota · 2003 [cited by examiner]
US 20040097658A1 · Everaerts · 2004 [cited by examiner]
US 20050152125A1 · Fukuda · 2005 [cited by applicant]
US 20060093797A1 · Sawatsky · 2006 [cited by examiner]
US 20080069949A1 · Glockner · 2008 [cited by examiner]
US 20080206504A1 · Hayes · 2008 [cited by examiner]
US 20090304948A1 · Witter · 2009 [cited by examiner]
US 20100103355A1 · Sakamoto · 2010 [cited by examiner]
US 20100119705A1 · Roche · 2010 [cited by examiner]
US 20110008547A1 · Grant · 2011 [cited by applicant]
US 20110126578A1 · Kim · 2011 [cited by examiner]
US 20110143047A1 · Kappaun · 2011 [cited by examiner]
US 20110249056A1 · Weingartner · 2011 [cited by applicant]
US 20120021193A1 · Lecolley · 2012 [cited by examiner]
US 20120090246A1 · Nunez-Regueiro · 2012 [cited by examiner]
US 20120197026A1 · Maeda · 2012 [cited by examiner]
US 20130008318A1 · McPherson · 2013 [cited by examiner]
US 20130034702A1 · Bockmeyer · 2013 [cited by examiner]
US 20130323477A1 · Depauw et al. · 2013 [cited by examiner]
US 20140146538A1 · Zenker · 2014 [cited by examiner]
US 20140357468A1 · Siebers · 2014 [cited by examiner]
US 20150225285A1 · Domey · 2015 [cited by examiner]
US 20150267079A1 · Bockmeyer · 2015 [cited by examiner]
US 20160145465A1 · Furutaka · 2016 [cited by applicant]
US 20160200625A1 · Miyasaka · 2016 [cited by examiner]
US 20160297222A1 · Allington · 2016 [cited by examiner]
US 20170001906A1 · Karagoz et al. · 2017 [cited by examiner]
US 20170031480A1 · Gabriel · 2017 [cited by applicant]
US 20170342282A1 · Torfs · 2017 [cited by applicant]
US 20180112906A1 · Yi · 2018 [cited by examiner]
US 20220227664A1 · Lambricht · 2022 [cited by examiner]
CN 1290281 · 2001 [cited by applicant]
CN 1644637 · 2005 [cited by applicant]
CN 101362917B · 2011 [cited by examiner]
CN 102390191 · 2012 [cited by applicant]
CN 103105676 · 2013 [cited by examiner]
CN 104936775 · 2015 [cited by applicant]
CN 105584245 · 2016 [cited by applicant]
DE 102016113162 · 2017 [cited by applicant]
DE 102016111162 · 2017 [cited by applicant]
EP 3034312 · 2016 [cited by applicant]
EP 3034312A1 · 2016 [cited by examiner]
IT MI20091870 · 2011 [cited by applicant]
JP 2002502201 · 2002 [cited by examiner]
WO 9850317 · 1998 [cited by applicant]
English machine translation CN103105676 (2013). [cited by examiner]
English machine translation CN101362917 (2011). [cited by examiner]
JP2002-502201 English machine translation (2002). [cited by examiner]
Arkles, B. “Tailoring Surfaces with Silanes”. Chemtech, Dec. 1977, vol. 7, pp. 766-778. (1977) (Year: 1977). [cited by examiner]