IP Library Granted Patent US 7,740,899
Granted Patent B2
US 7,740,899 · App. 10/431,346 · Granted Jun 22, 2010

Electronic device having lead and cadmium free electronic overglaze applied thereto

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Quick Facts
Patent No.
US 7,740,899
App. No.
10/431,346
Granted
Jun 22, 2010
Kind
B2
Abstract

The present invention provides an electronic device having a lead-free and cadmium-free glass composition applied thereto and fired to form an acid resistant overglaze, and a method of overglazing an electronic device using the lead-free and cadmium-free glass composition. The lead-free and cadmium-free glass composition fuses at low firing temperatures and is particularly suitable for use in thick film pastes. The glass composition forms predominantly bismuth titanate and/or zinc titanate crystals upon firing. Preferably, glass compositions include by weight from about 11% to about 52% SiO 2 , from 3.4% to about 40% TiO 2 , up to about 75% Bi 2 O 3 , up to about 40% by weight ZnO, where the sum of Bi 2 O 3 and ZnO comprises from about 15% to about 85% of the glass composition by weight.

Claims (21)

1. A method of forming a protective overglaze on a surface of an electronic device comprising:

applying a lead-free and cadmium-free glass composition to the surface of the electronic device; and

firing the glass composition to form the protective overglaze on the surface, wherein the glass composition comprises by weight from about 11% to about 52% SiO 2 , from 3.4% to about 40% TiO 2 , up to about 75% Bi 2 O 3 , up to about 45% by weight ZnO, provided the sum of Bi 2 O 3 and ZnO comprises from about 15% to about 85% of the glass composition.

2. The method according to claim 1 wherein the glass composition comprises by weight from about 14% to about 35% SiO 2 , from 3.4% to about 35% TiO 2 , from about 8% to about 74% Bi 2 O 3 , up to about 35% by weight ZnO, where the sum of Bi 2 O 3 and ZnO comprises from about 33% to about 74% of the glass composition by weight.

3. The method according to claim 1 wherein said glass composition further comprises one or more optional oxides selected from the group consisting of alkali metal oxides, B 2 O 3 , Al 2 O 3 , alkaline-earth metal oxides V 2 O 5 , Sb 2 O 3 , La 2 O 3 , Y 2 O 3 , Nb 2 O 5 , ZrO 2 , Cr 2 O 3 , Fe 2 O 3 , MnO 2 , CuO, NiO, Co 2 O 3 , CeO 2 , SnO, In 2 O 3 , and Mo 2 O 3 , provided that the total amount of said optional oxides present in said glass composition is limited to up to about 35% by weight, and further provided that the amount of alkali metal oxides is limited to up to 25% of the glass composition by weight, the amount of Bi 2 O 3 is limited to up to about 20% of the glass composition by weight, the amount of Al 2 O 3 is limited to up to about 15% of the glass composition by weight, the amount of alkaline-earth metal oxides is limited to a total of up to about 25% of the glass composition by weight, the amount of V 2 O 5 is limited to up to about 25% of the glass composition by weight, the amount of Sb 2 O 3 is limited to up to about 15% of the glass composition by weight, the amount of any one or a combination of the La 2 O 3 , Y 2 O 3 , Nb 2 O 5 , and ZrO 2 is limited to a total of up to about 25% of the glass composition by weight, the amount of any one or a combination of the Cr 2 O 3 , Fe 2 O 3 , MnO 2 , CuO, NiO, Co 2 O 3 , and CeO 2 is limited to a total of up to about 30% of the glass composition by weight, and the amount of any one or a combination of SnO, In 2 O 3 , and Mo 2 O 3 is limited to a total of up to about 20% of the glass composition by weight.

4. The method according to claim 2 wherein said glass composition further comprises a total of from about 0.1% to about 30% by weight of optional oxides, said optional oxides comprising by weight up to 13% alkali metal oxides, up to about 8% B 2 O 3 , up to about 13% Al 2 O 3 , a total of up to about 20% alkaline-earth metal oxides, up to about 10% V 2 O 5 , up to about 8% Sb 2 O 3 , a total of up to about 20% of any one or a combination of La 2 O 3 , Y 2 O 3 , Nb 2 O 5 , and ZrO 2 , a total of up to about 25% of any one or a combination of Cr 2 O 3 , Fe 2 O 3 , MnO 2 , CuO, NiO, Co 2 O 3 , CeO 2 , and a total of up to about 15% of any one or a combination of SnO, In 2 O 3 , and Mo 2 O 3 .

5. The method according to claim 1 wherein said glass composition is dispersed in a binder system to form a paste, and said paste further comprises one or more selected from the group consisting of inorganic pigments, fillers, and seeds for titanate crystals.

6. The method according to claim 1 wherein said glass composition comprises a combination of two or more glass frits.

7. A method of forming a protective overglaze on a surface of an electronic device comprising:

applying a lead-free and cadmium-free glass composition to the surface of the electronic device, wherein said glass composition comprises by weight from 3.4% to about 40% TiO 2 ; and

firing the glass composition at a temperature of from about 485° C. to about 850° C. to form the protective overglaze on the surface,

wherein the fired protective overglaze comprises a combination of residual glass and crystals, and wherein a predominant portion of said crystals comprise non-silicate crystals.

8. The method according to claim 7 wherein the residual glass comprises SiO 2 .

9. The method according to claim 7 wherein said non-silicate crystals comprise titanate crystals.

10. The method according to claim 9 wherein said titanate crystals comprise bismuth titanates and/or zinc titanates and/or bismuth vanadium titanates.

11. The method according to claim 7 wherein said glass composition further comprises from about 11% to about 52% SiO2, up to about 75% Bi 2 O 3 , up to about 45% by weight ZnO, where the sum of Bi 2 O 3 and ZnO comprises about 15% to about 85% of the glass composition by weight.

12. The method according to claim 11 wherein said glass composition comprises by weight from about 14% to about 35% SiO 2 , from 3.4% to about 35% TiO 2 , from about 8% to about 74% Bi 2 O 3 , up to about 35% by weight ZnO, where the sum of Bi 2 O 3 and ZnO comprises about 33% to about 74% of the glass composition by weight.

13. The method composition according to claim 7 wherein said glass composition further comprises one or more optional oxides selected from the group consisting of alkali metal oxides, B 2 O 3 , Al 2 O 3 , alkaline-earth metal oxides, V 2 O 5 , Sb 2 O 3 , La 2 O 3 , Y 2 O 3 , Nb 2 O 5 , ZrO 2 , Cr 2 O 3 , Fe 2 O 3 , MnO 2 , CuO, NiO, Co 2 O 3 , CeO 2 , SnO, In 2 O 3 , and Mo 2 O 3 , provided that the total amount of said optional oxides present in said glass composition is limited to up to about 35% by weight, and further provided that the amount of alkali metal oxides is limited to up to 25% of the glass composition by weight, the amount of B 2 O 3 , is limited to up to about 20% of the glass composition by weight, the amount of Al 2 O 3 , is limited to up to about 15% of the glass composition by weight, the amount of alkaline-earth metal oxides is limited to a total of up to about 25% of the glass composition by weight, the amount of V 2 O 5 is limited to up to about 25% of the glass composition by weight, the amount of Sb 2 O 3 is limited to up to about 15% of the glass composition by weight, the amount of any one or a combination of the La 2 O 3 , Y 2 O 3 , Nb 2 O 5 , and ZrO 2 is limited to a total of up to about 25% of the glass composition by weight ,the amount of any one or a combination of the Cr 2 O 3 , Fe 2 O 3 , MnO 2 , CuO, NiO, Co 2 O 3 , and CeO 2 is limited to a total of up to about 30% of the glass composition by weight, and the amount of any one or a combination of SnO, In 2 O 3 , and Mo 2 O 3 is limited to a total of up to about 20% of the glass composition by weight.

14. The method according to claim 12 wherein said glass composition further comprises a total of from about 0.1% to about 30% by weight of optional oxides, said optional oxides comprising by weight up to 13% alkali metal oxides, up to about 8% B 2 O 3 , up to about 13% Al 2 O 3 , a total of up to about 20% alkaline-earth metal oxides, up to about 10% V 2 O 5 , up to about 8% Sb 2 O 3 , a total of up to about 20% of any one or a combination of La 2 O 3 , Y 2 O 3 , Nb 2 O 5 , and ZrO 2 , a total of up to about 25% of any one or a combination of Cr 2 O 3 , Fe 2 O 3 , MnO 2 , CuO, NiO, Co 2 O 3 , and CeO 2 , and a total of up to about 15% of any one or a combination of SnO, In 2 O 3 , and Mo 2 3 .

15. The method according to claim 7 wherein said glass composition comprises a combination of two or more glass frits.

16. The method according to claim 7 wherein the lead-free and cadmium-free glass composition is applied to the surface of the electronic device in the form of a thick film paste.

Assignments (14)
SECURITY INTEREST Recorded May 2, 2022
From: CHROMAFLO TECHNOLOGIES CORPORATION; FERRO CORPORATION; FERRO ELECTRONIC MATERIALS INC.; PRINCE ENERGY LLC; PRINCE MINERALS LLC; PRINCE SPECIALTY PRODUCTS LLC
To: CREDIT SUISSE AG, CAYMAN ISLANDS BRANCH, AS ADMINISTRATIVE AGENT
Reel/Frame 059845/0082 →
RELEASE OF SECURITY INTEREST IN PATENTS RECORDED AT R/F 041736/0178 Recorded Apr 21, 2022
From: PNC BANK NATIONAL ASSOCIATION, AS COLLATERAL AGENT
To: FERRO CORPORATION
Reel/Frame 059747/0129 →
SECURITY INTEREST Recorded Feb 16, 2017
From: FERRO CORPORATION
To: PNC BANK, NATIONAL ASSOCIATION, AS COLLATERAL AGENT
Reel/Frame 041736/0178 →
RELEASE OF SECURITY INTEREST Recorded Feb 15, 2017
From: PNC BANK, NATIONAL ASSOCIATION, AS COLLATERAL AGENT
To: FERRO CORPORATION
Reel/Frame 041718/0307 →
PATENT SECURITY AGREEMENT Recorded Aug 12, 2014
From: FERRO CORPORATION
To: PNC BANK, NATIONAL ASSOCIATION
Reel/Frame 033522/0966 →
RELEASE OF SECURITY INTEREST IN PATENT COLLATERAL (RELEASES RF 017527/0934) Recorded Aug 12, 2014
From: PNC BANK, NATIONAL ASSOCIATION (AS SUCCESSOR-BY-MERGER TO NATIONAL CITY BANK)
To: FERRO CORPORATION
Reel/Frame 033522/0474 →
RELEASE OF SECURITY INTEREST IN PATENT COLLATERAL (RELEASES RF 017730/0620) Recorded Aug 12, 2014
From: PNC BANK, NATIONAL ASSOCIATION (AS SUCCESSOR-BY-MERGER TO NATIONAL CITY BANK)
To: FERRO CORPORATION
Reel/Frame 033522/0502 →
RELEASE OF SECURITY INTEREST IN PATENT COLLATERAL (RELEASES RF 024906/0728) Recorded Aug 12, 2014
From: PNC BANK, NATIONAL ASSOCIATION (AS SUCCESSOR-BY-MERGER TO NATIONAL CITY BANK)
To: FERRO CORPORATION
Reel/Frame 033522/0875 →
AMENDED AND RESTATED PATENT SECURITY AGREEMENT Recorded Aug 30, 2010
From: FERRO CORPORATION
To: PNC BANK NATIONAL ASSOCIATION (AS SUCCESSOR-BY-MERGER TO NATIONAL CITY BANK)
Reel/Frame 024906/0728 →
RELEASE OF SECURITY INTEREST Recorded Sep 29, 2008
From: THE BANK OF NEW YORK MELLON TRUST COMPANY, N.A. (AS SUCCESSOR-IN-INTEREST TO J.P. MORGAN TRUST COMPANY)
To: FERRO CORPORATION
Reel/Frame 021590/0591 →
SECURITY AGREEMENT Recorded Jun 15, 2006
From: FERRO CORPORATION
To: J.P. MORGAN TRUST COMPANY, NATIONAL ASSOCIATION, AS TRUSTEE
Reel/Frame 017794/0436 →
SECURITY AGREEMENT Recorded Jun 7, 2006
From: FERRO CORPORATION
To: NATIONAL CITY BANK, AS COLLATERAL AGENT
Reel/Frame 017730/0620 →
SECURITY AGREEMENT Recorded Apr 27, 2006
From: FERRO CORPORATION
To: NATIONAL CITY BANK, AS ADMINISTRATIVE AGENT
Reel/Frame 017527/0934 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 14, 2003
From: SRIDHARAN, SRINIVASAN; MOROZ, MICHAIL
To: FERRO CORPORATION
Reel/Frame 014389/0467 →