IP Library Granted Patent US 7,153,445
Granted Patent B2
US 7,153,445 · App. 10/028,955 · Granted Dec 26, 2006

Method for roughening copper surfaces for bonding to substrates

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Quick Facts
Patent No.
US 7,153,445
App. No.
10/028,955
Granted
Dec 26, 2006
Kind
B2
Abstract

The invention is directed to a method and composition for providing roughened copper surfaces suitable for subsequent multilayer lamination. A smooth copper surface is contacted with an adhesion promoting composition under conditions effective to provide a roughened copper surface, the adhesion promoting composition consisting essentially of an oxidizer, a pH adjuster, a topography modifier, and a uniformity enhancer. A coating promoter may be used in place of the uniformity enhancer or in addition to the uniformity enhancer. The adhesion promoting composition does not require a surfactant. The process may further comprise the step of contacting the uniform roughened copper surface with a post-dip, wherein the post-dip comprises an azole or silane compound or a combination of said azole and said silane. The post-dip may further comprise, alone or in combination, a titanate, zirconate, and an aluminate. The pH adjuster is preferably sulfuric acid and the oxidizer is preferably hydrogen peroxide. A hydrogen peroxide stabilizer may be used in the adhesion promoting composition.

Claims (29)

1. A process for preparing roughened copper surfaces suitable for subsequent multilayer lamination, said process comprising the steps of: contacting with a clean copper surface an adhesion promoting composition under conditions effective to provide a roughened copper surface, said adhesion promoting composition consisting essentially of:

hydrogen peroxide;

a pH adjuster;

a 5-membered aromatic fused N-heterocyclic ring compound, wherein the N-heterocyclic ring has a nitrogen atom at position 1 bonded to a hydrogen atom; and

a uniformity enhancer having the formula:

wherein R1 and R2 are independently selected from hydrogen or hydroxyl, amino, alkyl, hydroxyalkyl, aminoalkyl, nitroalkyl, mercaptoalkyl, or alkoxy groups;

wherein said adhesion promoting composition is at least essentially free of halogen ions.

2. The process according to claim 1 , wherein said process is preceded with the step of cleaning said copper surface.

3. The process according to claim 1 , wherein said process further comprises the step of contacting the uniform roughened copper surface with a post-dip.

4. The process according to claim 3 , wherein said post-dip comprises an azole or silane compound or a combination of said azole and said silane.

5. The process according to claim 4 , wherein said post-dip further comprises a titanate, zirconate, aluminate or a combination of said titanate, zirconate and aluminate.

6. The process of claim 4 , wherein said silane is selected from the group consisting essentially of

3-methylacryloyloxypropyltrimethoxysilane,

3-(N-styrylmethyl-2aminoethylamino) propyltrimethoxysilane hydrochloride,

3-(N-allyl-2-aminoethylamino)-propyltrimethoxysilane hydrochloride,

N-(styrylmethyl)-3-aminopropyltrimethoxysilane hydrochloride,

N-2-aminoethyl-3-aminopropyltrimethoxysilane,

3-(N-Benzyl-2-aminoethylamino)-propyltrimethoxy silane hydrochloride,

beta-(3,4-epoxycyclohexyl) ethyltrimethoxysilane, gamma-aminopropyl-triethoxy silane,

gamma-glycidoxypropyltrimethoxysilane, and

vinyltrimethoxysilane.

7. The process of claim 5 , wherein said titanate is selected from the group comprising titanate amine, tetraocytl di(ditridecyl)phosphito titanate, tetra(2,2-diallyloxymethyl) butyl-di(ditridecyl)phosphito titanate, and neopentyl(diallyl)oxy-tri (dioctyl)pyrophosphatotitanate, and neopentyl(diallyl)oxytri-(m-amino)phenyl titanate.

8. The process of claim 5 , wherein said zirconate is selected from the group comprising tetra (2,2 diallyloxymethyl)butyl, di(ditridecyl)phosphito zi rconate, neopentyl(diallyl)oxy, trineodecanoyl zirconate, neopentyl(diallyl)oxy, tri(dodecyl)benzene-sulfonyl zirconate, tetra (2,2 diallyloxymethyl)butyl-di (ditridecyl)phosphito zirconate, and zirconium IV 2,2-dimethyl 1 ,3-propanediol.

9. The process of claim 5 , wherein said aluminate is selected from the group comprising diisobutyl(oleyl)acetoacetylaluminate, and diisopropyl(oleyl)acetoacetyl aluminate.

10. The process according to claim 1 , wherein said uniformity enhancer is 5-aminotetrazole.

11. The process according to claim 1 , wherein said adhesion promoting composition further consists essentially of a copper salt.

12. The process according to claim 2 , wherein said step of cleaning said copper surface comprises the step of applying a cleaning solution to said copper surface.

13. The process according to claim 12 , wherein said step of cleaning said copper surface further comprises the step of draining excess cleaning solution from the copper surface.

14. The process according to claim 1 , wherein said uniformity enhancer is selected from the group consisting of 5-aminotetrazole; 5-methyltetrazole; 5-methylaminotetrazole; 1H-tetrazol-5-amine; 1H-tetrazol-5-amine, N, N-dimethyl-1 -methyltetrazole; 1-methyl-5-mercaptotetrazole, 1 ,5-dimethyltetrazole; 1-methyl-5-aminotetrazole; and 1-methyl-5-methylamino-tetrazole.

Assignments (16)
MERGER Recorded Jan 19, 2021
From: MACDERMID ENTHONE AMERICA LLC
To: MACDERMID, INCORPORATED
Reel/Frame 054951/0889 →
CHANGE OF NAME Recorded Jun 14, 2019
From: OMG ELECTRONIC CHEMICALS, LLC
To: MACDERMID ENTHONE AMERICA LLC
Reel/Frame 049477/0148 →
PATENT SECURITY AGREEMENT Recorded Feb 1, 2016
From: OMG ELECTRONIC CHEMICALS, LLC
To: BARCLAYS BANK PLC, AS COLLATERAL AGENT
Reel/Frame 037662/0086 →
TERMINATION AND RELEASE OF SECURITY INTEREST IN PATENTS Recorded Oct 28, 2015
From: PNC BANK
To: OMG ELECTRONIC CHEMICALS, LLC
Reel/Frame 036985/0566 →
SECURITY AGREEMENT Recorded Sep 12, 2013
From: OM GROUP, INC.; OMG ELECTRONIC CHEMICALS, LLC; OMG AMERICAS, INC.; EAGLEPICHER TECHNOLOGIES, LLC; EAGLEPICHER MEDICAL POWER, LLC
To: PNC BANK
Reel/Frame 031208/0876 →
RELEASE OF SECURITY INTEREST Recorded Sep 5, 2013
From: BANK OF AMERICA, N.A.
To: OM GROUP, INC.; EAGLEPICHER TECHNOLOGIES, LLC; EAGLEPICHER MEDICAL POWER, LLC; OMG AMERICAS, INC.; OMG ELECTRONIC CHEMICALS, LLC
Reel/Frame 031169/0976 →
SECURITY AGREEMENT Recorded Aug 12, 2011
From: OM GROUP, INC., A DELAWARE CORPORATION; COMPUGRAPHICS U.S.A. INC., A DELAWARE CORPORATION; CYANTEK CORPORATION, A DELAWARE CORPORATION; OMG AMERICAS, INC., A OHIO CORPORATION; OMG ELECTRONIC CHEMICALS, LLC, A DELAWARE LIMITED LIABILITY COMPANY; OMG ENERGY HOLDINGS, INC., A DELAWARE CORPORATION; OMG HARKO HOLDINGS, LLC, A DELAWARE LIMITED LIABILITY COMPANY; EAGLEPICHER MEDICAL POWER, LLC, A DELAWARE LIMITED LIABILITY COMPANY; EAGLEPICHER TECHNOLOGIES, LLC, A DELAWARE LIMITED LIABILITY COMPANY; EPEP HOLDING COMPANY, LLC, A DELAWARE LIMITED LIABILITY COMPANY
To: BANK OF AMERICA, N.A., AS COLLATERAL AGENT
Reel/Frame 026740/0353 →
PATENT RELEASE AGREEMENT Recorded Aug 10, 2011
From: PNC BANK, NATIONAL ASSOCIATION, AS ADMINISTRATIVE AGENT
To: OM GROUP, INC., A DELAWARE CORPORATION; OMG AMERICAS, INC., A OHIO CORPORATION; OMG ELECTRONIC CHEMICALS, INC., A DELAWARE LIMITED LIABILITY COMPANY; COMPUGRAPHICS U.S.A. INC., A DELAWARE CORPORATION; OMG ENERGY HOLDINGS, INC., A DELAWARE CORPORATION; EAGLEPICHER TECHNOLOGIES, LLC, A DELAWARE LIMITED LIABILITY COMPANY; EPEP HOLDING COMPANY, LLC, A DELAWARE LIMITED LIABILITY COMPANY; EAGLEPICHER MEDICAL POWER, LLC, A DELAWARE LIMITED LIABILITY COMPANY
Reel/Frame 026727/0485 →
CHANGE OF NAME Recorded Aug 11, 2010
From: OMG ELECTRONIC CHEMICALS, INC.
To: OMG ELECTRONIC CHEMICALS, LLC
Reel/Frame 024812/0920 →
SECURITY AGREEMENT Recorded Mar 11, 2010
From: OM GROUP, INC.; OMG AMERICAS, INC.; OMG ELECTRONIC CHEMICALS, INC.; COMPUGRAPHICS U.S.A. INC.; OM HOLDINGS, INC.; OMG ENERGY HOLDINGS, INC.; EAGLEPICHER TECHNOLOGIES, LLC; EPEP HOLDING COMPANY, LLC; EAGLEPICHER MEDICAL POWER, LLC
To: PNC BANK, NATIONAL ASSOCIATION
Reel/Frame 024066/0130 →
MERGER Recorded Jan 14, 2009
From: ELECTROCHEMICALS INC.; OMG FIDELITY, INC.
To: OMG ELECTRONIC CHEMICALS, INC.
Reel/Frame 022102/0711 →
TERMINATION AND RELEASE OF SECURITY INTEREST IN PATENT RIGHTS PREVIOUSLY RECORDED AT REEL 015667 FRAME 0177 Recorded Dec 31, 2007
From: CREDIT SUISSE FIRST BOSTON, ACTING THROUGH ITS CAYMAN ISLANDS BRANCH, AS ADMINISTRATIVE AGENT
To: ELECTROCHEMICALS, INC.
Reel/Frame 020299/0637 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 15, 2006
From: BERNARDS, ROGER; GONZALEZ, HECTOR; KUCERA, AL; SCHANHAAR, MIKE
To: ELECTROCHEMICALS INC.
Reel/Frame 018522/0359 →
SECURITY AGREEMENT Recorded Aug 10, 2004
From: ELECTROCHEMICALS, INC.
To: CREDIT SUISSE FIRST BOSTON, ACTING THROUGH ITS CAYMAN ISLANDS BRANCH, AS ADMINISTRATIVE AGENT
Reel/Frame 015667/0177 →
TERMINATION AND RELEASE OF SECURITY INTEREST IN PATENT RIGHTS (PREVIOUSLY RECORDED AT REEL 14289 FRAME 0742) Recorded Aug 4, 2004
From: JPMORGAN CHASE BANK, AS ADMINISTRATIVE AGENT
To: ROCKWOOD SPECIALTIES INTERNATIONAL, INC.; ROCKWOOD SPECIALTIES GROUP, INC.; ALPHAGARY CORPORATION; ADVANTIS TECHNOLOGIES, INC.; CHEMICAL SPECIALTIES, INC.; COMPUGRAPHICS U.S.A. INC.; CYANTEK CORPORATION; ELECTROCHEMICALS INC.; EXSIL, INC.; LUREX, INC.; ROCKWOOD AMERICA INC.; ROCKWOOD SPECIALTIES INC.; ROCKWOOD PIGMENTS NA, INC.; RS FUNDING CORPORATION; SOUTHERN CLAY PRODUCTS, INC.; SOUTHERN COLOR N.A., INC.
Reel/Frame 014943/0249 →
SECURITY AGREEMENT Recorded Jul 31, 2003
From: ROCKWOOD SPECIALTIES INTERNATIONAL, INC.; ROCKWOOD SPECIALTIES GROUP INC.; ALPHAGARY CORPORATION; ADVANTIS TECHNOLOGIES, INC.; CHEMICAL SPECIALTIES, INC.; COMPUGRAPHICS U.S.A. INC.; CYANTECK CORPORATION; ELECTROCHEMICALS INC.; EXSIL, INC.; LUREX, INC.; ROCKWOOD AMERICA INC.; ROCKWOOD SPECIALTIES INC.; ROCKWOOD PIGMENTS NA, INC.; RS FUNDING CORPORATION; SOUTHERN CLAY PRODUCTS, INC.; SOUTHERN COLOR N.A., INC.
To: JPMORGAN CHASE BANK
Reel/Frame 014289/0742 →