Surface mounting using partially cured B staged and fully cured C staged thermoplastic polyimide TPI adhesive compounds

1. A method for preparing a laminate by bonding two surfaces utilizing heat activated thermoplastic adhesive, said method comprising in combination:

A. providing a first laminate surface to be bonded;

B. providing a first liquid solution comprising a less than fully cured thermoplastic polyimide adhesive precursor polyamic acid polymer disposed in a solvent;

C. coating a layer of said first liquid solution upon said first surface;

D. fully curing said first liquid solution to form a layer of fully cured thermoplastic polyimide adhesive;

E. providing a second laminate surface to be bonded;

F. providing a second liquid solution comprising a less than fully cured thermoplastic polyimide adhesive precursor polyamic acid polymer disposed in a solvent;

G. coating a layer of said second liquid solution upon either said second laminate surface or said layer of fully cured thermoplastic polyimide;

H. partially curing said second liquid solution to a layer of partially cured thermoplastic polyimide adhesive comprising in combination:

a mixture of polyamic acid polymer and thermoplastic polyimide polymer solids disposed in said solvent, said mixture containing no less than 10% and no greater than 50% thermoplastic polyimide of the total polymer mass and said mixture further containing an amount of solvent of between 20 and 60% of the total mass of the mixture;

I. positioning said first and second laminate surfaces together to form an unbonded laminate wherein said partially cured layer of thermoplastic polyimide is disposed between second laminate surface and said fully cured layer of thermoplastic polyimide; and

J. applying heat and pressure to said unbonded laminate to:

i. outgas said solvent from said adhesive bondline;

ii. substantially convert all of said polyamic-acid polymer to said thermoplastic polyimide polymer, said conversion generating a quantity of water vapor;

iii. outgas said water vapor from said adhesive bondline; and

iv. bond said surfaces at the completion of said outgassing.

2. The method of claim 1 wherein the coefficient of thermal expansion of

one of said laminate surfaces is greater than the other.

3. The method of claim 1 further including the further step of applying additional higher pressure to said laminate to enhance said bond.

4. The method of claim 1 wherein said solvent is selected from the group consisting of N-methyl-2-pyrrolidone (NMP) and dimethylacetamide (DMAC).

5. The method of claim 1 wherein said polyamic acid polymer comprises a mixture of diamine and dianhydride monomers, said diamine monomer is selected from the group consisting of:

3 , 5 -diaminobenzoic acid (DABA), 3,3′-diaminobenzophenone (3,3′-DABP),3,4′-diaminobenzophenone (3,4′-DABP), 1,3-Bis (4-aminophenoxy) benzene (TPER), 3,4′-Oxydianiline (3,4′-ODA), 4,4′-Oxydianiline (4,4′-ODA), 4,4′-Methylene dianiline (4,4′-MDA), an aliphatic diamine, and a silicon-diamine; and said dianhydride monomer is selected from the group consisting of 3,3′,4,4′-Biphenyltetracarboxylic dianhydride (BPDA), 3,3′,4,4′-Benzophenone tetracarboxylic dianhydride (BTDA), 4,4′-Oxydiphthalic anhydride (ODPA), Pyromellitic dianhydride (PMDA), and 2,2′-Bis-(3,4-Dicarboxyphenyl) hexafluoropropane dianhydride (6FDA).

6. A method for preparing a laminate by bonding two surfaces utilizing a heat activated thermoplastic adhesive coated bondfilm, said method comprising in combination:

A. providing a substrate having first and second substrate surfaces;

B. providing a first liquid solution comprising a less than fully cured thermoplastic polyimide adhesive precursor polyamic acid polymer disposed in a solvent;

C. coating a layer of said first liquid solution upon said first substrate surface;

D. fully curing said first liquid solution to form a layer of thermoplastic polyimide adhesive on said first substrate surface;

E. providing a second liquid solution a less than fully cured thermoplastic polyimide adhesive precursor polyamic acid polymer disposed in a solvent;

F. coating a layer of said second solution upon said second substrate surface;

G. partially curing said second liquid solution to form a layer of thermoplastic polyimide adhesive on said second substrate surface comprising in combination:

a mixture of polyamic acid polymer and thermoplastic polyimide polymer solids disposed in said solvent, said mixture containing no less than 10% and no greater than 50% thermoplastic polyimide of the total polymer mass and said mixture further containing an amount of solvent of between 20 and 60% of the total mass of the mixture; said coated substrate comprising said bondfilm;

H. providing a first laminate surface to be bonded;

I. providing a second laminate surface to be bonded;

J. disposing said coated substrate comprising said bondfilm between said first and second laminate surfaces to form an unbounded laminate; and

K. applying heat and pressure to said unbonded laminate to:

i. outgas said solvent from said adhesive bondline;

ii. substantially convert all of said polyamic-acid polymer to said thermoplastic polyimide polymer, said conversion generating a quantity of water vapor;

iii. outgas said water vapor from said adhesive bondline; and

iv. bond said surfaces at the completion of said outgassing.

7. The method of claim 6 wherein the coefficient of thermal expansion of

one of said laminate surfaces is greater than the other.

8. The method of claim 6 further including the further step of applying additional higher pressure to said laminate to enhance said bond.

9. The method of claim 6 wherein said solvent is selected from the group consisting of N-methyl-2-pyrrolidone (NMP) and dimethylacetamide (DMAC).

10. The method of claim 6 wherein said polyamic acid polymer comprises a mixture of diamine and dianhydride monomers, said diamine monomer is selected from the group consisting of:

3,5-diaminobenzoic acid (DABA), 3,3′-diaminobenzophenone (3,3′-DABP), 3,4′-diaminobenzophenone (3,4′-DABP), 1,3-Bis(4-aminophenoxy)benzene (TPER), 3,4′-Oxydianiline (3,4′-ODA), 4,4′-Oxydianiline (4,4′-ODA), 4,4′-Methylene dianiline (4,4-MDA), an aliphatic diamine, and a silicon-diamine; and said dianhydride monomer is selected from the group consisting of 3,3′,4,4′-Biphenyltetracarboxylic dianhydride (BPDA), 3,3′,4,4′-Benzophenone tetracarboxylic dianhydride (BTDA), 4,4′-Oxydiphthalic anhydride (ODPA), Pyromellitic dianhydride (PMDA), and 2,2′-Bis-(3,4-Dicarboxyphenyl) hexafluoropropane dianhydride (6FDA).