CROSS-REFERENCE TO RELATED APPLICATIONS

This application claims the benefit of U.S. Provisional Application No. 60/755,174 filed Dec. 30, 2005; U.S. Provisional Application No. 60/755,249 filed Dec. 30, 2005; and U.S. Provisional Application No. 60/814,260 filed Jun. 16, 2006 which are each incorporated by reference in their entireties.

FIELD OF INVENTION

The present invention relates generally to polymer based substrates that can be selectively drilled (either wholly or partially) and/or surface ablated, using electromagnetic radiation, such as, amplified light (e.g., a laser), an electron beam or the like. More specifically, the compositions of the present invention comprise a drilled or ablated region that is sufficiently activated by the electromagnetic radiation to allow direct metalization (e.g., by electroless or electrolytic metal plating techniques) without requiring a separate metallization seed layer type step.

BACKGROUND INFORMATION

Electronic circuits are conventionally made from rigid epoxy-metal laminates, using a subtractive process. In such a process, a dielectric is typically layered with a solid metal layer, and thereafter, the metal layer is converted to a metal circuit pattern by subtracting away most of the metal using known lithography exposure and development (and/or etching) techniques. Such conventional methods can provide fine line conductive circuit patterns. However, such processes can be expensive, environmentally unfriendly, and increasingly problematic in meeting future requirements in the industry.

EP 1 367 872 A2 to Goosey et al. relates to laser activated dielectric materials and an electroless metal deposition process. This Goosey reference teaches the use of a sensitizing pre-dip and a milling process.

However, a need exists for an alternative, commercially practical method for creating reliable, metalized traces and vias (â€œviasâ€ are also known as and sometimes referred to herein as â€œinterconnectsâ€ ) without requiring the removal of relatively large amounts of metal during circuitization.

SUMMARY OF THE INVENTION

The present invention is directed to an electronic substrate having a polymer based layer. The polymer based layer comprises a heat stable, dielectric polymer in an amount within a range between (and optionally including) any two of the following: 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 96, and 97 weight-percent, based upon the total weight of the polymer based layer. Useful polymers in accordance with the present invention include polyimides, epoxy resins, silica filled epoxies, bismaleimide resins, ismaleimide triazines, fluoropolymers, polyesters, polyphenylene oxide/polyphenylene ether resins, polybutadiene/polyisoprene crosslinkable resins, liquid crystal polymers, polyamides, cyanate esters, and blends, derivations, combinations or copolymers thereof.

In addition to polymer, the polymer based layer further includes at least a plurality of non-conductive, non-activated crystal filler particles. The filler particles are present in an amount within a range between (and optionally including) any two of the following: 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 20, 25, 30, 35, 40, 45, 50, 55 and 60 weight-percent of the total weight of the polymer based layer.

The filler particles of the present invention have a non-homogeneous cationic component within the crystalline structure. Upon activation, such filler particles require no further processing to produce a commercially viable metallization surface.

The non-homogeneous cationic component has at least two different cationic components. In one embodiment, the first cationic component has a valence that is different from the valence of the second cationic component, and in such an embodiment, the first cationic component can be a metal that is different from the metal of the second cationic component. Generally, the first and second cationic components will be present within the crystalline filler particles in a ratio of 0.1-10:1.

In addition to the polymer based layer, the compositions of the present invention further include a conductive metal bonded to the polymer based layer along an interface. The interface is substantially devoid or otherwise free of a metallization seed layer other than a thin (generally less than 1000, 100, 80, 60, 50, 25, 10, 5, 4, 3, 2, 1 or 0.1 microns), continuous or discontinuous network of activated filler. The network of activated filler can be orderly, disorderly or a combination thereof. Once activated, the filler becomes substantially conductive (e.g., has a resistivity less than 0.001, 0.0001 or 0.00001 ohm-cm), whereas prior to activation, the filler is substantially dielectric (e.g., has a resistivity greater than 0.01, 0.1, 1.0 or 10.0 ohm-cm).

The activated filler is created by activating the non-activated crystal filler discussed above. The filler is activated using electromagnetic radiation. In accordance with the present invention, the electromagnetic radiation simultaneously drills or ablates the polymer based layer at precise, pre-defined locations, while simultaneously activating the non-activated multi-cation crystal filler. The surface defining the hole or indentation is effectively converted into a metallization seed layer, due to surface activation induced by the laser (or other high energy electromagnetic radiation). Hence, once the hole or indentation is created, it can then be immediately metalized, such as, by electroless and/or electrolytic metal plating, and the resulting metalized trace or via generally provides excellent electrical conducting performance, without the cost, expense and potential for error, inherent in a pre-dip (or other similar-type means for creating a seed layer that is separate and apart from the drilling or ablation step).

Other optional ingredients can also be incorporated into the polymer base layer of the present invention, such as, fillers, pigments, viscosity modifiers, and other additives common to the above described polymer systems, provided however that (depending upon the particular embodiment chosen) the total amount of optional ingredients does not exceed (or optionally is less than): 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 20, 25, 30, 35, 40, 45, 50, 55 or 60 weight-percent of the total weight of the polymer based layer.

Other features and advantages of the invention will be apparent from the following detailed description as well as the claims. The foregoing general description and the following detailed description are exemplary and explanatory only, and are not intended to be restrictive of the invention as defined in the appended claims.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT(S)Definitions

As used herein, the terms â€œcomprises,â€ â€œcomprising,â€ â€œincludes,â€ â€œincluding,â€ â€œhas,â€ â€œhavingâ€ or any other variation thereof, are intended to cover a non-exclusive inclusion. For example, a composition, a film, a composite, process, method, article, or apparatus that comprises a list of elements is not necessarily limited to only those elements but may include other elements not expressly listed or inherent to such process, method, article, or apparatus. Further, unless expressly stated to the contrary, â€œorâ€ refers to an inclusive or and not to an exclusive or. For example, a condition A or B is satisfied by any one of the following: A is true (or present) and B is false (or not present), A is false (or not present) and B is true (or present), and both A and B are true (or present). Also, use of the â€œaâ€ or â€œanâ€ are employed to describe elements and components of the invention. This is done merely for convenience and to give a general sense of the invention. This description should be read to include one or at least one and the singular also includes the plural unless it is obvious that it is meant otherwise.

As used herein, the term â€œfilmâ€ or â€œpolymer filmâ€ describes the physical form of the polymer composition, which may be flexible or rigid, and in roll or sheet form.

As used herein, the term â€œcompositionâ€ or â€œpolymer compositionâ€ describes a composition including various components, for example, multi cation crystal filler(s) and polymer binder(s).

As used herein, the term â€œcompositeâ€ describes a layered structure having at least one or more layers.

As used herein, the term â€œprepregâ€ means a woven glass or fiber-reinforced rigid dielectric layer with a partially cured B-stage polymer composition or a fully cured C-stage polymer composition. For example, a composition according to an aspect of the invention is impregnated into a woven glass structure to form a prepreg.

As used herein the term's FR-4 and FR-5 are chemically specific epoxy resins in a glass reinforced matrix, for example, copper clad epoxy impregnated glass fabric board in various grades classified by National Electrical Manufacturers Association (NEMA) which include FR-4 and FR-5.

As used herein the term â€œadjacentâ€ does not necessarily mean that a layer, member or structure is immediately next to another layer, member or structure. A combination of layer(s), member(s) or structure(s) that directly contact each other are still adjacent to each other.

As used herein, the term â€œDCâ€ means digital circuitry.

As used herein, the term â€œfunctional layerâ€ means a layer that has functional characteristics including, but not limited to: thermally conductive, dimensionally stable, adhesive, capacitive, resistive, and high frequency dielectric capability.

Unless otherwise defined, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs. Although methods and materials similar or equivalent to those described herein can be used in the practice or testing of the invention, suitable methods and materials are described below. All publications, patent applications, patents, and other references mentioned herein are incorporated by reference in their entirety. In case of conflict, the present specification, including definitions, will control. In addition, the materials, methods, and examples are illustrative only and not intended to be limiting.

Descriptions:

In one embodiment, the composition of the present invention is a light-activatable polymer composition comprises a heat stable, dielectric polymer binder and a crystalline filler. The heat stable, dielectric polymer binder has a dielectric constant less than (or less than and equal to) 10, 6.0, 5.0, 4.0, or 3.5, and sufficient heat stability that the polymer (or polymer blend) exhibits a change in modulus of less than 10, 8, 6, 5, 4, 3, 2, 1, or 0.1 percent when heated from a temperature of 20Â° C. to a temperature of 60, 70, 80, 90, 100, 125, 150, 175 or 200Â° C. Examples of such polymer binders can generally be selected from polyimides, epoxy resins, silica filled epoxy, bismaleimide resins, bismaleimide triazines, fluoropolymers, polyesters, polyphenylene oxide/polyphenylene ether resins, polybutadiene/polyisoprene crosslinkable resins (and copolymers), liquid crystal polymers, polyamides, cyanate esters, or combinations thereof, and a multi cation crystal filler. In this embodiment, the polymer binder is present in an amount between (and optionally including) any two of the following: 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 96 or 97 weight-percent of the total weight of the polymer composition. The filler is a multi-cation metal oxide crystal filler present in an amount between (and optionally, including) any two of the following: 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 20, 25, 30, 35, 40, 45, 50, 55 and 60 weight-percent of the total weight of the polymer composition.

Whereas conventional alumina, titania, silica and other substantially two component metal oxide, crystalline filler particles have a relatively simple crystalline structure which generally react (to the activation energy of the present invention) in a way that creates a surface requiring further processing before a commercially viable metallization surface is produced, the crystalline filler particles of the present invention comprise a complex crystalline structure having a non-homogeneous cationic structure. Such crystalline filler particles of the present invention are capable of acting effectively as a metallization seed layer, when activated by electromagnetic radiation in accordance with the present invention.

In one embodiment, a single-layer light-activatable polymer composite, includes a polymer composition comprising at least (or alternatively, comprising greater than): 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 96 or 97 weight-percent of a polymer binder selected from the group consisting of polyimide, epoxy resins, silica filled epoxy, bismaleimide resins, bismaleimide triazines, fluoropolymers, polyesters, polyphenylene oxide/polyphenylene ether resins, polybutadiene/polyisoprene crosslinkable resins (and copolymers), liquid crystal polymers, polyamides, cyanate esters, or combinations thereof, and a multi cation crystal filler. The weight percent of the filler, based on the total weight of the polymer composition used in the layer, is at least (or alternatively, is greater than): 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 20, 25, 30, 35, 40, 45, 50, 55 or 60 weight percent.

In another embodiment, a two-layer light-activatable polymer composite includes a first layer and a second layer; the first layer including a composition that includes at least (or alternatively, is greater than): 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 96 or 97 weight-percent of a polymer selected from polyimide, epoxy resins, silica filled epoxy, bismaleimide resins, bismaleimide triazines, fluoropolymers, polyesters, polyphenylene oxide/polyphenylene ether resins, polybutadiene/polyisoprene crosslinkable resins (and copolymers), liquid crystal polymers, polyamides, cyanate esters, or combinations thereof, the weight percent of the polymer binder based on the total weight of the polymer composition used in the first layer; and, at least (or alternatively, is greater than): 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 20, 25, 30, 35, 40, 45, 50, 55 or 60 weight-percent multi cation crystal filler based on the total weight of the polymer composition used in the first layer, and the second layer includes a functional layer.

In another embodiment, a three-layer light-activatable polymer composite includes two outer layers adjacent to an inner layer; the inner layer is positioned between the two outer layers, wherein at least one of the outer layers includes a polymer composition that includes at least (or alternatively, is greater than): 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 96 or 97 weight-percent of a polymer binder selected from polyimide, epoxy resins, silica filled epoxy, bismaleimide resins, bismaleimide triazines, fluoropolymers, polyesters, polyphenylene oxide/polyphenylene ether resins, polybutadiene/polyisoprene crosslinkable resins (and copolymers), liquid crystal polymers, polyamides, cyanate esters, or combinations thereof, the weight percent of the polymer binder based on the total weight of the polymer composition used in the one outer layer; and, at least (or alternatively, greater than): 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 20, 25, 30, 35, 40, 45, 50, 55 or 60 weight-percent (multi-cation metal oxide) filler based on the total weight of the polymer composition used in the one outer layer, and the inner layer (and optionally the other outer layer) is a functional layer.

Generally speaking, the activated (multi-cation metal oxide) filler is auto-catalytic, because it can effectively act as a seed layer or metalization catalyst immediately upon (electromagnetic) activation of the filler, and the activated fillers of the present invention can therefore be immediately used as a metallization seed layer without any need for further treatment or processing. Conventional laser activated fillers are often referred to as catalytic, but are generally not auto-catalytic, since conventional laser activated fillers generally require additional processing, such as the use of a pre-dip, before useful metallization is possible.

In another embodiment, a process for making a light-activatable polymer composition includes the steps of: dispersing a spinel type multi cation crystal filler in an organic solvent to form a dispersion where the average particle size of the spinel crystal filler is between (and optionally includes) any two of the following numbers 50, 100, 300, 500, 800, 1000, 2000, 3000, 4000, 5000 and 10000 nanometers; combining the dispersion with a polymer binder selected from polyimide, epoxy resins, silica filled epoxy, bismaleimide resins, bismaleimide triazines, fluoropolymers, polyesters, polyphenylene oxide/polyphenylene ether resins, polybutadiene/polyisoprene crosslinkable resins (and copolymers), liquid crystal polymers, polyamides, cyanate esters, or combinations thereof, to form a polymer composition; applying the polymer composition onto a portion of a flat surface to form a layer, and applying thermal energy to the layer to form a polymer composite.

In another embodiment, a process in accordance with the present invention further includes light-activating a portion of the polymer composite with a laser beam to form a light activated pattern on a surface of the composite, and metal plating the light activated pattern of the polymer composite using an electroless (or alternatively an electrolytic) plating bath to form electrically conductive pathways on the light activated pattern.

In one embodiment, a light-activatable polymer composition includes a polymer binder selected from a group consisting of: polyimide, epoxy resins, silica filled epoxy, bismaleimide resins, bismaleimide triazines, fluoropolymers, polyesters, polyphenylene oxide/polyphenylene ether resins, polybutadiene/polyisoprene crosslinkable resins, liquid crystal polymers, polyamides, cyanate esters, and combinations and copolymers thereof, the polymer binder being present in an amount between (and optionally also including) any two of the following: 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 96 or 97 weight-percent of the total weight of the polymer composition; and a spinel crystal filler present in an amount between (and optionally also including) any two of the following: 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 20, 25, 30, 35, 40, 45, 50, 55 and 60 weight-percent of the total weight of the polymer composition. The polymer composition has a visible-to-infrared light extinction coefficient between and including any two of the following numbers 0.05, 0.06, 0.07, 0.08, 0.09, 0.1, 0.2, 0.3, 0.4, 0.5, and 0.6 per micron.

In one embodiment, the spinel crystal filler is represented by the chemical formula AB₂O₄or BABO₄, where: i. the A component of the formulas is a metal cation having a valence of 2 and is selected from a group consisting of cadmium, zinc, copper, cobalt, magnesium, tin, titanium, iron, aluminum, nickel, manganese, chromium, and combinations of two or more of these; and ii. the B component of the formulas is a metal cation having a valence of 3, selected from a group consisting of cadmium, manganese, nickel, zinc, copper, cobalt, magnesium, tin, titanium, iron, aluminum, chromium, and combinations of two or more of these.

Alternatively, the A component is an element from the periodic table selected from a group consisting of cadmium, chromium, manganese, nickel, zinc, copper, cobalt, iron, magnesium, tin, titanium, and combinations of two or more of these, and the B component is an element from the periodic table selected from a group consisting of chromium, iron, aluminum, nickel, manganese, tin, and combinations of two or more of these.

The spinel crystal filler can have an average particle size between and including any two of the following numbers 50, 100, 300, 500, 800, 1000, 2000, 3000, 4000, 5000 and 10000 nanometers.

The composition may be impregnated into a glass structure to form a prepreg, may be impregnated into a fiber structure, or may be in the form of a film.

The film composites of the present invention may have a thickness between and including any two of the following numbers 1, 2, 3, 4, 5, 7, 8, 9, 10, 12, 14, 16, 18, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 100, 125, 150, 175 and 200 microns.

In another embodiment, a single-layer light-activatable polymer composite includes a polymer composition comprising at least 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 96, or 97 weight-percent of a polymer binder selected from the group consisting of polyimide, epoxy resins, silica filled epoxy, bismaleimide resins, bismaleimide triazines, fluoropolymers, polyesters, polyphenylene oxide/polyphenylene ether resins, polybutadiene/polyisoprene crosslinkable resins (and copolymers), liquid crystal polymers, polyamides, cyanate esters, or combinations thereof, the weight percent of the polymer binder based on the total weight of the polymer composition used in the first layer; and, at least 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 20, 25, 30, 35, 40, 45, 50, 55 or 60 weight-percent spinel crystal filler based on the total weight of the polymer composition.

The single layer polymer composite can have a visible-to-infrared light extinction coefficient between and including any two of the following numbers 0.05, 0.06, 0.07, 0.08, 0.09, 0.1, 0.2, 0.3, 0.4, 0.5, and 0.6 per micron. In another embodiment, the polymer composite can have a visible to ultraviolet light extinction coefficient between and including and two of the following numbers: 0.6 and 50 per micron. The single layer polymer composite includes a polymer binder, which can be a polyimide, epoxy resin, bismaleimide resin, bismaleimide triazine, a fluoropolymer, polyester, a liquid crystal polymer, a polyamide, a cyanate ester, or combinations, copolymers or derivations thereof.

In another embodiment, a two-layer light activatable polymer composite includes a first layer and a second layer, the first layer comprises a composition comprising at least (and alternatively, greater than) 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 96 or 97 weight-percent of a polymer binder selected from the group consisting of polyimide, epoxy resins, silica filled epoxy, bismaleimide resins, bismaleimide triazines, fluoropolymers, polyesters, polyphenylene oxide/polyphenylene ether resins, polybutadiene/polyisoprene crosslinkable resins (and copolymers), liquid crystal polymers, polyamides, cyanate esters, or combinations thereof, the weight percent of the polymer binder based on the total weight of the polymer composition used in the first layer; and, at least (and alternatively, greater than): 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 20, 25, 30, 35, 40, 45, 50, 55 or 60 weight-percent spinel crystal filler based on the total weight of the polymer composition used in the first layer, and the second layer comprises a functional layer. The first layer may be in the form of a film or a prepreg. The first layer can have a visible-to-infrared light extinction coefficient between (and optionally including) any two of the following numbers 0.05, 0.06, 0.07, 0.08, 0.09, 0.1, 0.2, 0.3, 0.4, 0.5, and 0.6 per micron. The second functional layer may be in the form of a film or prepreg. The second functional layer may also be a thermal conduction layer, a capacitor layer, a resistor layer, a dimensionally stable dielectric layer, or an adhesive layer.

In another embodiment, a three-layer light-activatable polymer composite includes two outer layers adjacent to an inner layer; the inner layer positioned between the two outer layers, wherein at least one of the outer layers comprises a polymer composition comprising at least (or alternatively, greater than) 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 96 or 97 weight-percent of a polymer binder selected from the group consisting of polyimide, epoxy resins, silica filled epoxy, bismaleimide resins, bismaleimide triazines, fluoropolymers, polyesters, polyphenylene oxide/polyphenylene ether resins, polybutadiene/polyisoprene crosslinkable resins (and copolymers), liquid crystal polymers, polyamides, cyanate esters, or combinations thereof, the weight percent of the polymer binder based on the total weight of the polymer composition used in the first layer; and at least (or alternatively, greater than) 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 20, 25, 30, 35, 40, 45, 50, 55 or 60 weight-percent spinel crystal filler based on the total weight of the polymer composition used in the first layer, and wherein in the inner layer (and optionally one of the outer layers) comprises a functional layer like a film or prepreg.

In another embodiment, a process for making a light-activatable polymer composition comprises the steps of: dispersing a spinel crystal filler in an organic solvent to form a dispersion, wherein the average particle size of the spinet crystal filler is between (and optionally including) any two of the following numbers 50, 100, 300, 500, 800, 1000, 2000, 3000, 4000, 5000 and 10000 nanometers; combining the dispersion with a polymer binder selected from the group consisting of polyimide, epoxy resins, silica filled epoxy, bismaleimide resins, bismaleimide triazines, fluoropolymers, polyesters, polyphenylene oxide/polyphenylene ether resins, polybutadiene/polyisoprene crosslinkable resins (and copolymers), liquid crystal polymers, polyamides, cyanate esters, or combinations thereof, to form a polymer composition; applying the polymer composition onto a portion of a flat surface to form a layer; and applying thermal energy to the layer to cure the polymer composition. The thermally exposed polymer composition may have a visible-to-infrared light extinction coefficient between and including any two of the following numbers 0.05, 0.06, 0.07, 0.08, 0.09, 0.1, 0.2, 0.3, 0.4, 0.5; and 0.6 per micron. The process may further include the steps of: light-activating a portion of the polymer composition with a laser beam to form light activated pattern on a surface of the composition, and metal plating the light activated pattern of the polymer composition using an electroless (or electrolytic) plating bath to form electrically conductive pathways on the light activated portions.

In yet another embodiment, a circuit board incorporates the polymer composition. The compositions may also be incorporated into a component selected from an integrated circuit package, an interconnect in a pin grid array, a multi-chip module, a chip-scale package, a ball grid array, a radio frequency module, a digital module, chip-on-flex, a stacked via substrate, a printed circuit board having embedded passive devices, a high density interconnect circuit board, an â€œLGAâ€ Land grid array, an â€œSOPâ€ (System-on Package) Module, a â€œQFNâ€ Quad Flat package-No Leads, and a â€œFC-QFNâ€ Flip Chip Quad Flat package-No leads, a component used in a high density interconnect, including a wafer scale package, a tape automated bonding circuit package, a chip-on-flex circuit package, or a chip-on-board electronic circuit package.

The compositions of the present invention may optionally further comprise an additive selected from the group consisting of an antioxidant, a light stabilizer, a light extinction coefficient modifier, a flame retardant additive, an anti-static agent, a heat stabilizer, a reinforcing agent, an ultraviolet light absorbing agent, an adhesion promoter, an inorganic filler, for example, silica, a surfactant or dispersing agent, or combinations thereof. Light extinction coefficient modifiers include, but are not limited to, carbon powder or graphite powder.

In one embodiment, the polymer compositions of the invention have dispersed therein highly light activatable spinel crystal fillers, where the fillers comprise two or more metal oxide cluster configurations within a definable crystal formation. The overall crystal formation, when in an ideal (i.e., non-contaminated, non-derivative) state, has the following general formula:

AB₂O₄

Where:

- i. A (in one embodiment, A is a metal cation having primarily, if not exclusively, a valance of 2) is selected from a group including cadmium, chromium, manganese, nickel, zinc, copper, cobalt, iron, magnesium, tin, titanium, and combinations thereof, which provides the primary cation component of a first metal oxide cluster (â€œmetal oxide cluster 1â€ ) typically a tetrahedral structure,
- ii. B (in one embodiment, B is a metal cation having primarily, if not exclusively, a valance of 3) is selected from the group including chromium, iron, aluminum, nickel, manganese, tin, and combinations thereof and which provides the primary cation component of a second metal oxide cluster (â€œmetal oxide cluster 2â€ ) typically an octahedral structure,
- iii. where within the above groups A or B, any metal cation having a possible valence of 2 can be used as an â€œAâ€ , and any metal cation having a possible valence of 3 can be used as a â€œBâ€ ,
- iv. where the geometric configuration of â€œmetal oxide cluster 1â€ (typically a tetrahedral structure) is different from the geometric configuration of â€œmetal oxide cluster 2â€ (typically an octahedral structure),
- v. where a metal cation from A and B can be used as the metal cation of â€œmetal oxide cluster 2â€ (typically the octahedral structure), as in the case of an â€˜inverseâ€™ spinel-type crystal structure,
- vi. where O is primarily, if not exclusively, oxygen; and
- vii. where the â€œmetal oxide cluster 1â€ and â€œmetal oxide cluster 2â€ together provide a singular identifiable crystal type structure having heightened susceptibility to electromagnetic radiation evidenced by the following property, when dispersed in a polymer-based dielectric at a loading of about 10 to about 30 weight percent, a â€œvisible-to-infrared lightâ€ extinction coefficient can be measure to be between and including any two of the following numbers, 0.05, 0.06, 0.07, 0.08, 0.09, 0.1, 0.2, 0.3, 0.4, 0.5 and 0.6 per micron.

The spinel crystal fillers can be dispersed in a polymer binder solution. The polymer binder solution includes polyimide, epoxy resins, silica filled epoxy, bismaleimide resins, bismaleimide triazines, fluoropolymers, polyesters, polyphenylene oxide/polyphenylene ether resins, polybutadiene/polyisoprene crosslinkable resins (and copolymers), liquid crystal polymers, polyamides, cyanate esters, or combinations thereof, dissolved in a solvent. The fillers are typically dispersed at a weight-percent between (and optionally including) any two of the following numbers 3, 5, 7, 9, 10, 12, 15, 20, 25, 30, 35, 40, 45, 50, 55 and 60 weight-percent of the polymer, and initially have an average particle size (after incorporation into the polymer binder) of between (and optionally including) any two of the following numbers 50, 100, 300, 500, 800, 1000, 2000, 3000, 4000, 5000 and 10000 nanometers.

The spinel crystal fillers can be dispersed in an organic solvent (either with or without the aid of a dispersing agent) and in a subsequent step, dispersed in a polymer binder solution to form a blended polymer composition. The blended polymer composition can then be cast onto a flat surface (or drum), heated, dried, and cured or semi-cured to form a polymer film with a spinet crystal filler dispersed therein.

The polymer film can then be processed through a light activation step by using a laser beam. The laser beam can be focused, using optical elements, and directed to a portion of the surface of the polymer film where a circuit-trace, or other electrical component, is desired to be disposed. Once selected portions of the surface are light-activated, the light-activated portions can be used as a path (or sometimes a spot) for a circuit trace to be formed later, by a metal plating step, e.g., an electroless plating step.

The number of processing steps employed to make a circuit using the polymer film or polymer composites of the present invention are often far fewer relative to the number of steps in known subtractive processes commonly employed in the industry today.

In one embodiment, the polymer compositions and polymer composites have a visible-to-infrared light extinction coefficient of between and including any two of the following numbers 0.05, 0.06, 0.07, 0.08, 0.09, 0.1, 0.2, 0.3, 0.4, 0.5, and 0.6 per micron (or 1/micron). Visible-to-infrared light is used to measure a light extinction coefficient for each film. The thickness of the film is used in the calculations for determining the light extinction coefficient.

As used herein, the visible-to-infrared light extinction coefficient (sometimes referred to herein to simply as â€˜alphaâ€™) is a calculated number. This calculated number is found by taking the ratio of measured intensity of a specific wavelength of light (using a spectrometer) after placing a sample of the composite film in a light beam path, and dividing that number by the light intensity of the same light through air.

If one takes the natural log of this ratio and multiplies it by (âˆ’1), then divides that number by the thickness of the film (measured in Microns), a visible-to-infrared light extinction coefficient can be calculated.

The general equation for the visible-to-infrared light extinction coefficient is then represented by the general formula:

Alpha=âˆ’1Ã—[ln(I(X)/I(O))]/t

- where I(X) represents the intensity of light transmitted through a film,
- where I(O) represents the intensity of light transmitted through air, and
- where t represents the thickness of a film.

Typically, the film thickness in these calculations is expressed in microns. Thus, the light extinction coefficient (or alpha number) for a particular film is expressed as 1/microns, or inverse microns (e.g., microns^âˆ’1). Particular wavelengths of light useful in the measurements discussed herein are typically those wavelengths of light covering the visible-to-infrared light portion of the spectrum.

The polymer compositions and polymer composites comprise spinel crystal fillers, substantially homogeneously dispersed, in a polymer binder solution in an amount within a range between (and including) any two of the following weight-percentages 3, 4, 5, 6, 7, 8, 9, 10, 12, 15, 18, 20, 24, 25, 28, 30, 32, 34, 35, 36, 38, 40, 42, 44, 46, 48, 50, 52, 54, 56, 58 and 60 weight-percent. Polymer composites containing too much spinel crystal filler can sometimes be too brittle to handle in downstream processing as the composites tend to lose flexibility with higher loadings of filler.

In one embodiment, the spinel crystal fillers are represented by the general formula:

AB₂O₄

where A is a metal cation typically having a valence 2, and is selected from a group comprising cadmium, chromium, manganese, nickel, zinc, copper, cobalt, iron, magnesium, tin, titanium, and combinations of two or more of these, and where B is a metal cation typically having a valence of 3, and is selected from the group comprising chromium, iron, aluminum, nickel, manganese, tin, and combinations of two or more of these, and where O is primarily, if not in all cases, oxygen.

In one embodiment, the metal cation A provides the primary cation component of a first metal oxide cluster, â€œmetal oxide cluster 1â€ (typically a tetrahedral structure) of a spinel structure. Metal cation B provides the primary cation component of a second metal oxide cluster, â€œmetal oxide cluster 2â€ (typically an octahedral structure).

In another embodiment, within the above groups A and B, any metal cation having a possible valence of 2 can be used as an â€œAâ€ cation. In addition, any metal cation having a possible valence of 3 can be used as a â€œBâ€ cation provided that the geometric configuration of â€œmetal oxide cluster 1â€ is different from the geometric configuration of â€œmetal oxide cluster 2â€ .

In yet another embodiment, A and B can be used as the metal cation of â€œmetal oxide cluster 2â€ (typically the octahedral structure). This is true in the particular case of an â€˜inverseâ€™ spinel-type crystal structure typically having the general formula B(AB)O₄.

In one or more steps, a polymer binder is solvated to a sufficiently low viscosity (typically, a viscosity of less than 50, 40, 30, 20, 15, 10, 9, 8, 7, 6, 5, 4, 3, 2, 1.5, 1, 0.5, 0.1, 0.05, and 0.001 kiloPoise) to allow the spinel crystal filler (which can also be suspendable in a similar or the same solvent) to be adequately dispersed within the polymer binder solution. The dispersion of the spinel crystal filler is conducted in such a manner as to avoid undue agglomeration of the particles in the solution or the dispersion. Unwanted agglomeration of the filler particles can cause unwanted interfacial voids, or other problems in the polymer composite.

The spinel crystal filler particles can be dispersed in the polymer binder solution directly, or can be dispersed in a solvent prior to dispersion in the polymer binder solution. The filler particles can be mixed in a solvent to form a dispersion, until the particles have reached an average particle size of between any two of the following numbers 50, 100, 300, 500, 800, 1000, 2000, 3000, 4000, 5000, and 10000 nanometers. The dispersion may then be mixed using a high-speed, or high-shear, mixing apparatus. Spinel crystal filler may be dispersed using various suitable solvents. In some cases, the dispersions may also include one or more suitable dispersing agents known to a skilled artisan for assistance in forming a stable dispersion, particularly for commercial scale production.

The spinel crystal fillers dispersed in the polymer binder solution generally have an average particle size between and including any two of the following numbers 50, 100, 200, 250, 300, 350, 400, 450, 500, 1000, 2000, 3000, 4000, 5000 and 10000 nanometers. Generally, at least 80, 85, 90, 92, 94, 95, 96, 98, 99 or 100 percent of the dispersed spinel crystal filler is within the above size range(s). Crystal size, in the polymer binder solution, can be determined by a laser particle analyzer, such as an LS130 particle size analyzer with small volume module made by COULTERÂ®.

The polymer binder solution and the spinel crystal filler particles are combined to form a relatively uniform dispersion of the composition. The composition may then be converted as described below into a polymer composite where the solids content is typically greater than 98.0, 98.5, 99.0 or 99.5 weight-percent.

Because some spinel crystal fillers are easily dispersed in a polymer binder solution, with little or no additional shearing force required, slurries formed can contain often fewer than 100, 50, 20, 10, 8, 6, 5, 4, 3, 2, or 1 parts per million (ppm) undesired agglomerates. Undesirable agglomerates are defined as a collection of bound (adjoining) spinel crystal fillers having an average particle size of greater than 10, 11, 12, 13, 14, or 15 microns. However, some spinel crystal fillers may require some milling or filtration to break up unwanted particle agglomeration for adequately dispersing nano-sized fillers into a polymer. Milling and filtration can be costly, and may not satisfactorily remove all unwanted agglomerates. Thus, in one embodiment, the spinel crystal filler is dispersible, and suspendable, at 20 weight-percent in a (at least 99 weight-percent pure) dimethylacetamide solvent. After dispersing and suspending the spinel crystal filler into a solvent (optionally with the aid of a high-shear mechanical mixer) less than 15, 10, 8, 6, 4, 2 or 1 weight-percent of the filler particles by weight can precipitate out of solution when the solution was kept at rest for 72 hours at 20Â° C.

The present invention employs the use of a selected group of spinet crystal fillers to allow for efficient and accurate surface patterning through activation by a laser (or other similar type light patterning technique) prior to bulk metallization of the pattern formed by the laser.

In one embodiment, a light extinction coefficient modifier can be added as a partial substitute for some, but not all, of the spinel crystal filler. Appropriate amounts of substitution can range from, between and including any two of the following numbers, 1, 2, 3, 4, 5, 10, 15, 20, 25, 30, 35, or 40 weight percent of the total amount of spinel crystal filler component. In one embodiment, about 10 weight percent of the spinel crystal filler can be substituted with a carbon powder or graphite powder. The polymer composite formed therefrom should have a sufficient amount of spinel crystal structure present in the polymer composite to allow metal ions to plate effectively on the surface thereof, while the above mentioned amount of substitute (e.g., carbon powder) darkens the polymer composite sufficiently enough so that a sufficient amount of light energy (i.e., an amount of light energy that effectively light activates the surface of the composite) can be absorbed.

A specific range of useful light extinction coefficients has been advantageously found for the polymer compositions and polymer composites. Specifically, it was found that the polymer compositions and polymer composites require a sufficient degree of light-absorption capability to work effectively in high-speed light activation steps typically employing the use of certain laser machines.

For example, in one type of light-activation step employed (e.g., a step employing the use of a laser beam) it was found that the polymer compositions and composites of the present invention are capable of absorbing a significant amount of light energy so that a well-defined circuit trace pattern can be formed thereon. This can be done in a relatively short time. Conversely, commercially available polymer films (i.e., films without these particular fillers, or films containing non-functional spinel crystal fillers) may take longer, have too low a light extinction coefficient, and may not be capable of light-activating in a relatively short period, if at all. Thus, many polymer films, even films containing relatively high loadings of other types of spinel crystal fillers, may be incapable of absorbing enough light energy to be useful in high-speed, light activation manufacturing, as well as being able to receive plating of a metal in well-defined circuit patterns.

A wide range of polymer binders suitable for use in the embodiments of the invention include polyimide, epoxy resins, silica filled epoxy, bismaleimide resins, bismaleimide triazines, fluoropolymers, polyesters, polyphenylene oxide/polyphenylene ether resins, polybutadiene/polyisoprene crosslinkable resins (and copolymers), liquid crystal polymers, polyamides, cyanate esters, or combinations thereof. The polymer binders may include an inorganic filler, for example, silica or alumina. A wide range of polymer binders was found to be particularly useful in the preparation of the polymer compositions and composites.

Useful organic solvents for the preparation of the polymer binders of the invention should be capable of dissolving the polymer binders. A suitable solvent should also have a suitable boiling point, for example, below 225Â° C., so the polymer solution can be dried at moderate (i.e., more convenient and less costly) temperatures. A boiling point of less than 210, 205, 200, 195, 190, 180, 170, 160, 150, 140, 130, 120 and 110Â° C. is suitable.

As described above, suitable polymer binders for use in the embodiments of the invention include polyimide, epoxy resins, silica filled epoxy, bismaleimide triazine (BT), fluoropolymers, polyesters, polyphenylene oxide/polyphenylene ether resins, polybutadiene/polyisoprene crosslinkable resins (and copolymers), liquid crystal polymers, polyamides, and cyanate esters.

Epoxy resins are thermoplastic materials which can be cured to a thermoset polymer. Major resin types include diglycidyl ethers of bisphenol A, novolacs, peracid resins, and hydantoin resins, among others. There are many epoxy resin suppliers in the world and the most recognizable trade names include Araldite, DER, Epi-Cure, Epi-Res, Epikote, Epon, Epotuf, each of which provide a wide range of properties depending on the formulation and processing. Additional components may also be added to an epoxy resin and curing agent formulation. These components include, but are not limited to, diluents, resinous modifiers to affect flexibility, toughness or peel strength, adhesion fillers, colorants, dyes, rheological additives, and flame retardants.

In one embodiment, the polymer binder may include an epoxy resin. Examples of suitable epoxy resins, include, but are not limited to, glycidyl ether type epoxy resin, glycidyl ester resin and glycidylamine type epoxy resin. In addition, any silica or alumina-filled epoxies are also suitable.

Examples of suitable glycidyl ether type epoxy resins include, but are not limited to: bisphenol A type, bisphenol F type, brominated bisphenol A type, hydrogenated bisphenol A type, bisphenol S type, bisphenol AF type, biphenyl type, naphthalene type, fluorene type, phenol novolac type, cresol novolac type, DPP novolac type, trifunctional type, tris(hydroxyphenyl)methane type, and tetraphenylolethane type epoxy resins.

Examples of suitable glycidyl ester type epoxy resins include, but are not limited to: hexahydrophthalate type and phthalate type epoxy resins.

Examples of suitable glycidylamine type epoxy resins include, but are not limited to: tetraglycidyldiaminodiphenylmethane, triglycidyl isocyanurate, hydantoin type, 1,3-bis(N,N-diglycidylaminomethyl) cyclohexane, aminophenol type, aniline type, and toluidine type epoxy resins.

In one embodiment, the polymer binder may include a polyester. Examples of suitable polyesters include, but are not limited to: polyethylene terephthalate, polybutylene terephthalate, poly(trimethylene)terephthalate, etc., poly(âˆˆ-caprolactone), polycarbonate, poly(ethylene-2,6-naphthalate), poly(glycolic acid), poly(4-hydroxy benzoic acid)-co-poly(ethyleneterephthalate) (PHBA), and poly(hydroxybutyrate).

In another embodiment, the polymer binder may include a polyamide. Examples of suitable aliphatic polyamides include, but are not limited to: nylon 6, nylon 6,6, nylon 6,10 and nylon 6,12, nylon 3, nylon 4,6 and copolymers thereof are useful with this invention. Examples of aliphatic aromatic polyamides include, but are not limited to, nylon 6T (or nylon 6(3)T), nylon 10T and copolymers thereof, nylon 11, nylon 12 and nylon MXD6 are also suitable for use with this invention. Examples of aromatic polyamides include, but are not limited to, poly(p-phenylene terephthalamide), poly(p-benzamide), and poly(m-phenylene isophthalamide) are also suitable for use with this invention.

In another embodiment, the polymer binder may include a fluoropolymer. The term fluoropolymer is intended to mean any polymer having at least one, if not more, fluorine atoms contained within the repeating unit of the polymer structure. The term fluoropolymer, or fluoropolymer component, is also intended to mean a fluoropolymer resin (i.e. a fluoro-resin). Commonly, fluoropolymers are polymeric material containing fluorine atoms covalently bonded to, or with, the repeating molecule of the polymer. Suitable fluoropolymer components include, but are not limited to:

- 1. â€œPFAâ€ , a poly(tetrafluoroethylene-co-perfluoro[alkyl vinyl ether]), including variations or derivatives thereof, having the following moiety representing at least 50, 60, 70, 80, 85, 90, 95, 96, 97, 98, 99 or about 100 weight percent of the entire polymer:

- â€ƒwhere R₁is C_nF_2n+1, where n can be any natural number equal to or greater than 1 including up to 20 or more, typically n is equal to 1 to three, where x and y are mole fractions, where x is in a range from 0.95 to 0.99, typically 0.97, and where y is in a range from 0.01 to 0.05, typically 0.03, and where the melt flow rate, described in ASTM D 1238, is in a range of from 1 to 100 (g/10 min.), preferably 1â€² to 50 (g/10 min.), more preferably, 2 to 30 (g/10 min.), and most preferably 5 to 25 (g/10 min.).
- 2. â€œFEPâ€ , a poly(tetrafluoroethylene-co-hexafluoropropylene) [a.k.a. poly(tetrafluoroethylene-co-hexafluoropropylene) copolymer], derived in whole or in part from tetrafluoroethylene and hexafluoropropylene, including variations or derivatives thereof, having the following moiety representing at least 50, 60, 70, 80, 85, 90, 95, 96, 97, 98, 99 or about 100 weight percent of the entire polymer:

- â€ƒwhere x and y are mole fractions, where x is in a range from 0.85 to 0.95, typically 0.92, and where y is in a range from 0.05 to 0.15, typically 0.08, and where the melt flow rate, described in ASTM D 1238, is in a range of from 1 to 100 (g/10 min.), preferably 1 to 50 (g/10 min.), more preferably, 2 to 30 (g/10 min.), and most preferably 5 to 25 (g/10 min.). The FEP copolymer can be derived directly or indirectly from: (i.) 50, 55, 60, 65, 70 or 75 percent to about 75, 80, 85, 90 or 95 percent tetrafluoroethylene; and (ii.) 5, 10, 15, 20, or percent to about 25, 30, 35, 40, 45 or 50 percent (generally 7 to 27 percent) hexafluoropropylene. Such FEP copolymers are well known and are described in U.S. Pat. Nos. 2,833,686 and 2,946,763.
- 3. â€œPTFEâ€ , a polytetrafluoroethylene, including variations or derivatives thereof, derived in whole or in part from tetrafluoroethylene and having the following moiety representing at least 50, 60, 70, 80, 85, 90, 95, 96, 97, 98, 99 or about 100 weight percent of the entire polymer: where x is equal to any natural number between 50 and 500,000.
- 4. â€œETFEâ€ , a poly(ethylene-co-tetrafluoroethylene), including variations or derivatives thereof, derived in whole or in part from ethylene and tetrafluoroethylene and having the following moiety representing at least 50, 60, 70, 80, 85, 90, 95, 96, 97, 98, 99, or about 100 weight percent of the entire polymer:

î¢ (CH₂â€”CH₂)_xâ€”(CF₂â€”CF₂)_yî¢

- â€ƒwhere x and y are mole fractions, where x is in a range from 0.40 to 0.60, typically 0.50, and where y is in a range from 0.40 to 0.60, typically 0.50, and where the melt flow rate, described in ASTM D 1238, is in a range of from 1 to 100 (g/10 min.), preferably 1 to 50 (g/10 min.), more preferably, 2 to 30 (g/10 min.), and most preferably 5 to 25 (g/10 min.).

Advantageous characteristics of fluoropolymer resins include high-temperature stability, resistance to chemical attack, advantageous electrical properties (high-frequency properties in particular) low friction properties, and low tackiness. Other potentially useful fluoropolymer resins include the following:

- 1. chlorotrifluoroethylene polymer (CTFE);
- 2. tetrafluoroethylene chlorotrifluoroethylene copolymer (TFE/CTFE);
- 3. ethylene chlorotrifluoroethylene copolymer (ECTFE);
- 4. polyvinylidene fluoride (PVDF);
- 5. polyvinylfluoride (PVF); and
- 6. TeflonÂ® AF (sold by E.I. du Pont de Nemours & Co.).

In yet another embodiment, the polymer binder may include a liquid crystal polymer or thermotropic liquid crystal polymer. Liquid crystal polymers generally include a fusible or melt processible polyamide or polyester. Liquid crystal polymers also include, but are not limited to, polyesteramides, polyesterimides, and polyazomethines. Suitable liquid crystal polymers are described by Jackson et al. in U.S. Pat. Nos. 4,169,933, 4,242,496 and 4,238,600, as well as in â€œLiquid Crystal Polymers VI: Liquid Crystalline Polyesters of Substituted Hydroquinones.â€ The term â€œthermotropicâ€ means a polymer that when tested by the TOT test as described in U.S. Pat. No. 4,075,262 transmits light through crossed polarizers and is thus considered to form an anisotropic melt. Suitable liquid crystal polymers are described, for example in U.S. Pat. Nos. 3,991,013; 3,991,014; 4,011,199; 4,048,148; 4,075,262; 4,083,829; 4,118,372; 4,122,070; 4,130,545; 4,153,779; 4,159,365; 4,161,470; 4,169,933; 4,184,996; 4,189,549; 4,219,461; 4,232,143; 4,232,144; 4,245,082; 4,256,624; 4,269,965; 4,272,625; 4,370,466; 4,383,105; 4,447,592; 4,522,974; 4,617,369; 4,664,972; 4,684,712; 4,727,129; 4,727,131; 4,728,714; 4,749,769; 4,762,907; 4,778,927; 4,816,555; 4,849,499; 4,851,496; 4,851,497; 4,857,626; 4,864,013; 4,868,278; 4,882,410; 4,923,947; 4,999,416; 5,015,721; 5,015,722; 5,025,082; 5,1086,158; 5,102,935; 5,110,896 and U.S. Pat. No. 5,143,956; and European Patent Application 356,226. Commercial examples of liquid crystal polymers include the aromatic polyesters or polyester-amides) sold under the trademarks ZeniteÂ® (DuPont), VECTRAÂ® (Hoechst), and XYDARÂ® (Amoco).

In another embodiment, the polymer binders of the present invention may include a cyanate ester. An example of a suitable cyanate ester includes, but is not limited to, dicyanobisphenol A and 4,4â€²-isopropyl bis(phenyl cyanate). Modification of this basic structure can be used to provide various engineering properties, including but not limited to toughness, rigidity, and elevated glass transition temperature. Upon heating these monomers, prepolymers are obtained, which are typically triazine resins. Upon further heating highly crosslinked polycyanurate is formed with a glass transition temperature in the 240-290Â° C. range. The resins may be used by themselves or in blends with epoxy. For certain electronic applications, at least three polymers based on cyanate esters are used: a cyanate ester homopolymer, a copolymer of cyanate ester with bismaleimide (known as a bismaleimide triazine (BT) resin), and bismaleimide.

The polymer binders of the present invention, when dissolved in a suitable solvent to form a polymer binder solution (and/or casting solution), may also contain one or more additives. These additives include, but are not limited to, processing aids, antioxidants, light stabilizers, light extinction coefficient modifiers, flame retardant additives, anti-static agents, heat stabilizers, ultraviolet light absorbing agents, inorganic fillers, for example, silicon oxides, adhesion promoters, reinforcing agents, and a surfactant or dispersing agent, and combinations thereof.

The polymer solution can be cast or applied onto a support, for example, an endless belt or rotating drum, to form a film layer. The solvent-containing film layer can be converted into a self-supporting film by baking at an appropriate temperature (which may be thermal curing) or simply by drying (or partial drying known as â€œB-stageâ€ ) which produces a substantially dry film. Substantially dry film, as used herein, is a defined as a film with less than 2, 1.5, 1.0, 0.5, 0.1, 0.05, or 0.01 weight-percent volatile (e.g., solvent or water) remaining in the polymer composite. In addition, thermoplastic polymer compositions, having the spinel crystal filler dispersed therein, can be extruded to form either a film or any other pre-determined shaped article.

In one embodiment, a polymer film (polymer composite) is made having a thickness of between (and optionally including) any two of the following numbers: 1, 2, 3, 4, 5, 7, 8, 9, 10, 12, 14, 16, 18, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 100, 125, 150, 175 and 200 microns.

When the spinel crystal fillers are dispersed in a polymer binder, for example, at a loading level of about 10 to about 30 weight percent, a â€œvisible-to-infrared lightâ€ extinction coefficient is measured to be, between and including any two of the following numbers, 0.05, 0.06, 0.07, 0.08, 0.09, 0.1, 0.2, 0.3, 0.4, 0.5 and 0.6 per micron.

In the embodiments of the invention, the spinel crystal fillers described allow for good metal-ion deposition onto an already light-activated pathway (formed in a relatively short period via a laser beam). In addition, the spinel crystal fillers provide a visible-to-infrared light extinction coefficient to the composite that provides functionality in high-speed light activation process (i.e., â€˜light activationâ€™ is performed easily with relatively low levels of light).

In accordance with the invention, the polymer binder is chosen to provide important physical properties to the composition and polymer composite. Beneficial properties include, but are not limited to, good adhesiveness (i.e., metal adhesion or adhesion to a metal), high and/or low modulus (depending upon the application), high mechanical elongation, a low coefficient of humidity expansion (CHE), and high tensile strength.

As with the polymer binder, the spinel crystal filler can also be specifically selected to provide a polymer composite having a well-defined light-activated pathway after intense light-energy has been applied. For example, a well-defined light-activated pathway can more easily produce well-defined circuit metal traces after the light-activated material is submerged in an electroless-plating bath. Metal is typically deposited onto the light-activated portion of the surface of the polymer composite via an electroless-plating step.

In one embodiment, the polymer compositions of the invention are used to form a multi-layer (at least two or more layers) polymer composite. The multi-layer polymer composite can be used as at least a portion of a printed circuit board (â€œPCBâ€ ), chip scale package, wafer scale package, high density interconnect board (HDI), module, â€œLGAâ€ Land grid array, â€œSOPâ€ (System-on Package) Module, â€œQFNâ€ Quad Flat package-No Leads, â€œFC-QFNâ€ Flip Chip Quad Flat package-No leads, or other similar-type electronic substrate. Printed circuit boards (either covered with, or incorporating therein, the polymer composites) may be single sided, double sided, may be incorporated into a stack, or a cable (i.e. a flexible circuit cable). Stacks can include several individual circuits to form what is commonly referred to as a multi-layer board. Any of these types of circuits may be used in a solely flexible or rigid circuit or, or may be combined to form a rigid/flex or flex/rigid printed wiring board or cable.

In the case of a three-layer polymer composite, the spinel crystal filler can be in the outer layers, the inner layer, in at least two-layers, or in all three layers. In addition, the concentration (or loading) of the spinel crystal filler can be different or the same in each individual layer, depending on the final properties desired.

In one embodiment, electromagnetic radiation (i.e., light-energy via a laser beam) is applied to the surface of the polymer composite. In one embodiment, a polymer film or composite can be light activated using a commercially available, Esko-Graphics CyrelÂ® Digital Imager (CDI). The imager can be operated in a continuous wave mode or can be operated in a pulse mode. The purpose of applying this energy, on a particular predetermined portion of the film, is to light-activate the film surface. As defined herein, the term light-activated is defined as a portion of a surface on a polymer composite, wherein a metal ion can bond to the surface in a manner capable of forming a metal circuit trace. If only a small amount of metal is electroless plated onto the light activated portion of a surface of the film, and is thereby rendered incapable of forming an electrically conductive pathway, the film may not be considered as â€˜light-activatableâ€™ for purposes herein.

A 50-watt Yttrium Aluminum Garnet (YAG) laser may be employed to light activate the polymer composites. However, other types of lasers can be used. In one embodiment, a YAG laser (e.g. Chicago Laser Systems Model CLS-960-S Resistor Trimmer System) can be used to emit energy between 1 and 100 watts, ranging at about 355, 532 or 1064 nm wavelengths light. Generally, the wavelength of the laser light useful to light-activate a portion of the surface of a polymer composite can range from a wavelength between and including any two of the following numbers 200 nm, 355 nm, 532 nm, 1064 nm, or 3000 nm.

Generally, a laser beam can be modulated using an acousto-optic modulator/splitter/attenuator device (AOM) and can produce up to 23 watts in a single beam. The polymer composites can be held in place by vacuum, or by adhesive (or both), on the outer surface of a drum or metal plate. A drum-type assembly can rotate the film at speeds ranging from 1 to 2000 revolutions per minute in order to reduce production time. Spot size (or beam diameter) of the laser beam can be at a focus distance of from between, and including, any two of the following numbers, 1, 2, 4, 6, 8, 10, 15, 20 or 25 microns, typically 18 or 12 microns. Average exposures (e.g. energy dose) can be from between, and including, any two of the following numbers 0.1, 0.5, 1.0, 2, 4, 6, 8, 10, 15 or 20 J/cm². In the examples, at least 4 and 8 J/cm²were used.

A digital pattern of a printed circuit board, known as an image file, can be used to direct light to desired portions (i.e., locations) on the surface of a polymer composite. Software may be used to store information regarding the location of lines, spaces, curves, pads, holes, and other information such as pad diameter, pad pitch, and hole diameter. This data may be stored in digital memory that is readily accessible to AOM electronic devices.

The movement of the laser light may be controlled by a computer and is directed in an organized, predetermined, pixel-by-pixel (or line-by-line) manner across a panel or composite surface. The fine features, e.g., less than 100, 75, 50 or 25 microns in line width, of a circuit pattern are inscribed on a surface of the polymer composite. A combination of light sources, scanning, beam modulation, digital pattern transfer, and mechanical conditions stated above, may all be used to provide the desired particular circuit pattern.

In one embodiment, metal is subsequently applied to the light-activated portions of the polymer composites. For these polymer composites, metal can be plated onto a surface using an â€˜electrolessâ€™ plating bath in an electroless-plating step. The plating baths may include a copper ion source, a reducing agent, an oxidizing agent, and a chelating agent, in addition to trace amounts of other additives.

Variables that can control the speed and quality in which a plating bath can plate metal onto a surface of a film include, but are not limited to the temperature of the plating bath, the amount of surface to be plated, the chemical balance of the solution (e.g., replenishing the plating solution with a substance that has been consumed), and the degree of mechanical agitation. The temperature range of a plating bath can be controlled at a temperature between room temperature and about 70 to 80Â° C. The temperature can be adjusted according to the type, and amount, of chelating agent (and other additives) used.

Digitally imaged circuits can be electroless copper plated by using a single-step or two-step process. First, the polymer compositions or composites of the present invention are digitally imaged by a light activation step. Light activation debris, or miscellaneous particles, can be removed by mechanical brushing, air or ultra-sonification in order for a clean electroless copper-plating step to begin. After these initial steps have been taken, the light-activated polymer compositions or composites can be submerged into an electroless copper-plating bath at a plating rate of approximately >3 microns/hour.

The advantages of the present invention are illustrated in the following non-limiting Examples. The processing and test procedures used in the preparation and testing of the composites containing the polymer binders and spinel crystal fillers are described below.

EXAMPLES

The following examples were prepared from a polymer binder blended with a dispersion of the below mentioned spinel crystal filler.

Example 1

A metal oxide slurry was prepared by first, dissolving 25 grams of dispersant Disperbyk-192 (a copolymer with pigment affinic groups made by BYK-Chemie GmbH) in 247.5 grams of acetone in a Netzsch commercially available media mill. The solvent was stirred at 1000 rpms. 250 grams of fine copper chromite spinel, CuCr₂O₄powders (Shepherd Black 20C980) was added and allowed to mix for about 30 minutes. After the above milling process, the mean primary particle size in the slurry was measured to be 0.664 microns. This is slurry is used in the following sample preparations.

Sample A: A 10 weight % filled epoxy composition was prepared by dissolving 7.20 grams of Dyhardna 100SF (used as hardener, a Cyanoguanidine with anticaking agent from Degussa AG) and 10.80 grams of Dyhardâ„¢ UR500 (used as accelerator, a Carbamide compound from Degussa AG) in 162.00 grams of Eponâ„¢ 862 (a Bisphenol-F/Epichlorohydrin epoxy resin from Resolution Performance Products, LLP). The composition of Dyhardâ„¢ UR500 consists of >80% N,Nâ€³-(4-methyl-m-phenylene) bis(Nâ€²,Nâ€²-dimethylurea). After the attainment of a homogeneous and viscous organic medium, 20 grams of the pre-dispersed copper chromite spinel powder slurry was added, and mixed thoroughly by hand or with a commercially available mixer. The above composition was further processed on a three-roll mill to achieve a paste of consistent viscosity and dispersion. The viscosity for this composition was approximately 30-100 PaÂ·S measured on a Brookfield HBT viscometer using a #5 spindle at 10 rpm and 25Â° C.

Sample B: A 10 weight % spinel filled epoxy composition was prepared by dissolving 7.12 grams of Dyhardâ„¢ 100SF (used as hardener, a Cyanoguanidine with anticaking agent from Degussa AG) and 10.68 grams of Dyhardâ„¢ UR500 (used as accelerator, a Carbamide compound from Degussa AG) in 160.2 grams of Eponâ„¢ 862 (a Bisphenol-F/Epichlorohydrin epoxy resin from Resolution Performance Products, LLP). The composition of Dyhardâ„¢ UR500 consisted of >80% N,Nâ€³-(4-methyl-m-phenylene) bis(Nâ€²,Nâ€²-dimethylurea). After the attainment of a homogeneous and viscous organic medium, 20 grams of the pre-dispersed copper chromite spinel powder slurry and 2 grams of soya lecithin (a surfactant from Central Soya Inc.) was added, and mixed thoroughly by hand or a commercially available mixer. The above composition was further processed on a three-roll mill to achieve a paste of consistent viscosity and dispersion. The viscosity for this composition was approximately 30-100 PaÂ·S measured on a Brookfield HBT viscometer using a #5 spindle at 10 rpm and 25Â° C.

Sample C: A 10 weight % filled epoxy composition was prepared by using the above ingredients: Dyhardâ„¢ 100SF, Dyhardâ„¢ UR500, Eponâ„¢ 862, and pre-dispersed copper chromite spinel slurry. The surfactant was changed to a phosphate ester (RE-610 from Rhone Poulenc Inc) at the amount of, respectively, 7.12 grams, 10.68 grams, 160.2 grams, 20 grams, and 2 grams.

Sample D: A 10 weight % filled epoxy composition was prepared by using the above ingredients: Dyhardâ„¢ 100SF, Dyhardâ„¢ UR500, Eponâ„¢ 862, and pre-dispersed copper chromite spinel slurry. The surfactant was changed to a defoamer, 2-heptanone (from Eastman Chemicals) in the amount of 7.12 grams, 10.68 grams, 160.2 grams, 20 grams, and 2 grams, respectively.

Sample E: Following the above procedure, a 5 weight % filled composition was prepared by using the above ingredients of Dyhardâ„¢ 100SF, Dyhardâ„¢ UR500, Eponâ„¢ 862, pre-dispersed copper chromite spinel slurry, and soy lecithin in the amounts of 7.52 grams, 11.28 grams, 169.2 grams, 10 grams, and 2 grams, respectively.

Sample F: A 20 weight % filled epoxy composition was prepared by using the above ingredients of Dyhardâ„¢ 100SF, Dyhardâ„¢ UR500, Eponâ„¢ 862, pre-dispersed copper chromite spinel slurry, and soy lecithin in the amounts of 6.32 grams, 9.48 grams, 142.2 grams, 40 grams, and 2 grams, respectively.

Sample G: A 30 weight % filled epoxy composition was prepared by using the above ingredients of Dyhardâ„¢ 100SF, Dyhardâ„¢ UR500, Eponâ„¢ 862, pre-dispersed copper chromite spinel slurry, and soy lecithin in the amounts of 5.52 grams, 8.28 grams, 124.2 grams, 60 grams, and 2 grams, respectively.

The above roll-milled paste compositions were separately coated by a doctor blade on a 5-mil thick KaptonÂ® polyimide carrier film to achieve a uniform thickness in the range of 2.5 to 3.0 mils without pinholes, bubbles, or other visible defects. These thicker sample films were for DC imaging work. A separate set of thinner coating films was also prepared in the range of 0.5 to 2.0 mils with doctor blade for the optical density (OD) measurement whose data are used to calculate the extinction coefficient for this series of CuCr₂O₄spinel filled epoxy samples. After settling for 10 minutes, the coated samples were heated for 1 hour at 150Â° C. to complete the curing of the epoxy medium.

The data is summarized in TABLE 1 below.

TABLE 1FillerExampleSpinelloadingFilmAbsorption#1Filled(weight-ThicknesscoefficientPlateabilitySampleEpoxypercent)(microns)(alpha)(Y = yes)â€‚1ACuCr₂O₄1013.80.1218Yâ€‚2ACuCr₂O₄10190.1357Yâ€‚3ACuCr₂O₄10144.40.0616Yâ€‚4BCuCr₂O₄1010.60.1694Yâ€‚5BCuCr₂O₄1045.20.1167Yâ€‚6BCuCr₂O₄10470.1053Yâ€‚7CCuCr₂O₄1013.80.1268Yâ€‚8CCuCr₂O₄1012.40.143Yâ€‚9CCuCr₂O₄1041.20.1269Y10DCuCr₂O₄1055.60.1015Y11ECuCr₂O₄514.80.0731Y12ECuCr₂O₄532.60.0509Y13ECuCr₂O₄546.20.0493Y14FCuCr₂O₄2015.40.2153Y13ECuCr₂O₄546.20.0493Y14FCuCr₂O₄2015.40.2153Y15FCuCr₂O₄2043.60.2039Y16GCuCr₂O₄3021.10.3416Y17GCuCr₂O₄3012.70.3699Y18GCuCr₂O₄3016.30.3221Y

When using a DuPont Cyrel Digital Imager, the laser imageability and copper plateability are summarized below for Samples A-G at any thickness.

Energy Dosage (J/cm²)Samples246810AfaintgoodgoodgoodgoodBfaintgoodgoodgoodgoodCnofaintgoodgoodgoodDfaintgoodgoodgoodgoodEfaintgoodgoodgoodgoodFgoodgoodgoodgoodgoodGgoodgoodgoodgoodgood

It is to be understood that although the above examples employ one type of epoxy resin, the example is exemplary only. The epoxy resin used represents a vast family of various epoxy resins.

Example 2

A metal oxide slurry was prepared by dissolving 25 grams of dispersant Disperbyk-192 (a copolymer with pigment affinic groups made by BYK-Chemie GmbH) in 247.5 grams of acetone in a Netzsch commercially available media mill. The solvent was stirred at 1000 rpms. 250 grams of fine copper chromite spinel, CuCr₂O₄powders (Shepherd Black 20C980) was added and allowed to mix for about 30 minutes. After the above milling process, the mean primary particle size in the slurry was measured to be 0.664 microns. This slurry is the slurry used in the following sample preparations.

Bismaleimide/triazine (BT) resins are reaction products of Bismaleimide and dicyanobisphenol A leading to structures containing triazine and diazine rings. These are sold as BT resins by Mitsubishi Chemical and are classified as a cyanate ester. BT has a Tg of about 195Â° C. and can provide an operating temperature of about 160Â° C. The BT resin solution acquired for this DC study is consisted of 70 weight % resin and 30 weight % Methyl Ethyl Ketone (MEK) as solvent.

In order to raise the viscosity of the BT resin solution, MEK was evaporated in a fume hood with magnetic stirring at room temperature. The choice of room temperature evaporation was to assure no undesirable thermal effect to change the physical and chemical nature of the BT resin in the as-received solution. A 20.5 hour evaporation removed 7.03 weight % MEK to provide a 75.29 weight % BT resin solution. This process was found to increase the viscosity of BT resin solution to obtain a filled BT of adequate viscosity for more acceptable coating for digital circuitry imaging.

Three compositions, H, I, and J, were made to provide 5, 10, and 20 weight % CuCr₂O₄spinel in BT resin. The actual amounts were calculated with the needed BT resin quantity after deducting the volatile MEK solvent which should be nearly completely removed after the subsequent step of solvent drying at 80Â° C. CuCr₂O₄spinel powders were easily dispersed in the BT resin solution and suitable methods for mixing inorganic materials with organic binder solutions were used. Due to the high volatility of the solvent MEK used in the BT resin solution, however, the dispersion apparatus/method should provide full or semi-enclosure of the treated materials to minimize the loss of MEK which will raise the overall viscosity and/or form surface skin. Specific sample preparation procedures are described below.

Sample H: 50 grams of 5 weight % CuCr₂O₄spinel in BT resin composition was prepared by mixing 2.50 grams of the above CuCr₂O₄spinel powder slurry in 63.09 grams of the previously concentrated BT resin solution (with 75.29 weight % BT resin in MEK). Although the total amount of the added ingredients was 65.59 grams, after discounting the volatile MEK solvent, the remaining CuCr₂O₄spinel and BT resin yielded the specified quantity of 50 grams.

Sample I: 50 grams of 10 weight % CuCr₂O₄spinel in BT resin composition was prepared by mixing 5.00 grams of the above CuCr₂O₄spinel powder slurry in 59.77 grams of the previously concentrated BT resin solution (with 75.29 weight % BT resin in MEK). Although the total amount of the added ingredients was 64.77 grams, after discounting the volatile MEK solvent, the remaining CuCr₂O₄spinel and BT resin yielded the specified quantity of 50 grams.

Sample J: 50 grams of 20 weight % CuCr₂O₄spinel in BT resin composition was prepared by mixing 10.00 grams of the above CuCr₂O₄spinel powder slurry in 53.13 grams of the previously concentrated BT resin solution (with 75.29 weight % BT resin in MEK). Although the total amount of the added ingredients was 63.13 grams, after discounting the volatile MEK solvent, the remaining CuCr₂O₄spinet slurry and BT resin yielded the specified quantity of 50 grams.

A parallel group of three compositions, K, L and M, were also prepared to provide 5, 20, and 30 weight % CuCr₂O₄spinet in BT resin with the addition of 1 weight % soya lecithin as a surfactant. The actual amounts were calculated with the needed BT resin quantity after deducting the volatile MEK solvent which should be nearly completely removed after the subsequent step of solvent drying at 80 degrees C. To maintain the desired weight % of CuCr₂O₄spinel, the soya lecithin surfactant was added at the expense of the BT resin. Specific sample preparation procedures are described below.

Sample K: 50 grams of 5 weight % CuCr₂O₄spinel in BT resin composition was prepared by mixing 2.50 grams of the above CuCr₂O₄spinel powder slurry in 62.42 grams of the previously concentrated BT resin solution (with 75.29 weight % BT resin in MEK) and 0.5 grams of soya lecithin as surfactant. Although the total amount of the added ingredients was 65.42 grams, after discounting the volatile MEK solvent, the remaining CuCr₂O₄spinel and BT resin yielded the specified quantity of 50 grams.

Sample L: 50 grams of 20 weight % CuCr₂O₄spinet in BT resin composition was prepared by mixing 10.00 grams of the above CuCr₂O₄spinet powder slurry in 52.46 grams of the previously concentrated BT resin solution (with 75.29 weight % BT resin in MEK) and 0.5 grams of soya lecithin as surfactant. Although the total amount of the added ingredients was 62.96 grams, after discounting the volatile MEK solvent, the remaining CuCr₂O₄spinet and BT resin yield the specified quantity of 50 grams.

Sample M: 50 grams of 30 weight % CuCr₂O₄spinel in BT resin composition was prepared by mixing 15.00 grams of the above CuCr₂O₄spinel powder slurry in 45.82 grams of the previously concentrated BT resin solution (with 75.29 weight % BT resin in MEK) and 0.5 grams of soya lecithin as surfactant. Although the total amount of the added ingredients was 61.32 grams, after discounting the volatile MEK solvent, the remaining CuCr₂O₄spinel and BT resin yield the specified quantity of 50 grams.

For DC imaging work, a one millimeter thick copper foil was used as a carrier layer. The above H to M compositions were separately coated by a doctor blade to achieve a uniform thickness in the range of 2.5 to 3.0 mils without pinholes, bubbles, or other visible defects. After settling for 10 minutes, the coated samples were heated for 1 hour at 80Â° C. to evaporate the MEK solvent contained in the BT resin solution, followed by a 90 minute curing at 200Â° C. of the BT resin as recommended by the manufacturer.

A separate set of thinner coating films were also prepared in the range of 0.5 to 2.0 mils on a 5-mil thick KaptonÂ® polyimide carrier film with doctor blade for the optical density (OD) measurement whose data are used to calculate the extinction coefficient for this series of CuCr₂O₄spinel filled BT samples.

The data for the spinel-filled BT resin is summarized in Table 2 below.

TABLE 2FillerExampleSpinelloadingFilmAbsorptionPlateability#2Filled BT(weight-Thicknesscoefficient(Y = yes,Sampleresinpercent)(microns)(alpha)N = no)19HCuCr₂O₄528.20.0282N20ICuCr₂O₄1021.40.0533Y21JCuCr₂O₄20200.082Y22KCuCr₂O₄527.40.0295N23LCuCr₂O₄2024.40.0904Y24MCuCr₂O₄3025.30.1233Y25MCuCr₂O₄3027.80.1224YFor Table 1 and Table 2, assuming no light scattering, I_x= I_o* e^{(âˆ’Î±*x)}; T = I_x/I_o= 10^(âˆ’OD)= e^{(âˆ’Î±*x)}; a = âˆ’[LN(10(âˆ’OD))]/x; and OD = âˆ’LOG(T).

When using a DuPont Cyrel Digital Imager, the laser imageability and copper plateability are summarized below for Samples I, J, L, and M (Workable examples) and H, and K (Comparative examples).

Workable Examples

Energy Dosage (J/cm²)Sample468101520IfaintfaintgoodgoodfairfairJfairfairgoodgoodgoodgoodLfairgoodgoodgoodgoodfairMfairgoodgoodgoodgoodgood

Comparative Examples

Energy Dosage (J/cm²)Sample468101520HnonononononoKnononononono

Example 26

A metal oxide slurry was prepared by first adding 13.09 L of dimethyl acetamide (DMAc) to a KadyÂ® Mill commercially available kinetic dispersion mixer. The solvent was stirred at 1000 rpms. A 10 weight-percent polyamic acid solution, dissolved in DMAc, was then added to the mill to aid in ultimately stabilizing the filler dispersion. Finally, 499.62 g of fine (CuFe)(CrFe)₂O₄powder (PK 3095 from Ferro Co. GmBh) was added and allowed to mix for about 30 minutes.

0.81 gallons of the above slurry was then well dispersed, and uniformly mixed, using a GreercoÂ® mixer, into 5.19 gallons of 17 weight-percent polyamic acid solution dissolved in DMAc.

After thorough mixing of the filler dispersion in the polyamic acid polymer, the viscosity of the mixed polymer was raised to about 1000 poise by adding an additional amount of pyromellitic dianhydride (dissolved in a 6 weight-percent solution).

Next, a thin sheet of mixed polymer (containing spinel crystal filler) was cast onto a 316 stainless belt to form a wet film. The thickness of the wet film was adjusted in order to obtain a dry film thickness of about a 2 mil (50 microns).

The metal belt was heated in an oven and ramped from 90Â° C. to 140Â° C. over about 15 minutes. The film was peeled from the belt and pinned on a tenter frame (a thermal-processing oven) where the edges of the film were bound.

Then, the tentered film was further heated to dry (>99% solids) and imidize the film by transporting it through a drying oven which was ramped from 200Â° C. to in excess of 350 C over a Ëœ30 minute period. This final thin film contained approximately 3 percent by weight (CuFe)(CrFe)₂O₄powder (PK 3095 from Ferro Co. GmBh) in polyimide.

Example 27

A metal oxide slurry was prepared by first adding 13.09 L of dimethyl acetamide (DMAc) to a KadyÂ® Mill kinetic dispersion mixer. The solvent was stirred at 1000 rpms. A 10 weight-percent polyamic acid solution in DMAc, was then added to the mill to aid in the dispersion of the filler. The viscosity of the polymer was 100 poise prior to mixing and 29.78 kg of the polyamic acid solution was used. Finally, 499.62 g of fine (CuFe)(CrFe)₂O₄powder (PK 3095 from Ferro Co. GmBh) was added and allowed to mix for about 30 minutes.

A talc slurry was then prepared by adding 4.07 L of dimethyl acetamide (DMAc) and 386 g of talc. The slurry was added to the KadyÂ® Mill. The dispersion was stirred at 1000 rpms. A 10 weight-percent polyamic acid solution in DMAc was then added to the beaker to aid in the dispersion of the filler. The viscosity of the polymer was 100 poise prior to mixing. In this case, 9.27 kg of the polyamic acid solution was used.

1.17 gallons of the above metal oxide slurry was combined and uniformly mixed, using a GreercoÂ® mixer, into 3.75 gallons of 17 weight-percent polyamic acid solution dissolved in DMAc. The viscosity of this polymer solution was also 100 poise prior to mixing with the slurry.

After thorough dispersion of the filler in the polyamic acid polymer, the viscosity of the mixed polymer was raised to 1000 poise by adding an additional amount of PMDA (dissolved in a 6 percent by weight solution).

Next, a thin sheet of mixed polymer was cast onto a 316 SS belt to form a wet film. The thickness of the wet film was adjusted in order to obtain a dry film thickness of about two mils (50 microns).

The metal belt was heated in an oven and ramped from 90Â° C. to 140Â° C. over Ëœ15 minutes. The film was peeled from the belt and pinned on a tenter frame where the edges of the film were bound.

Then, the film was further heated to dry (>99% solids) and imidize the film by transporting it through a drying oven which was ramped from 200Â° C. to in excess of 350 C over a Ëœ30 minute period.

This final thin film contained approximately 5 percent by weight (CuFe)(CrFe)₂O₄powder (PK 3095 from Ferro Co. GmBh) and 5 percent by weight of talc powder in polyimide.

FillerInfrared LightExampleloadingFilmextinction coef-#Spinel Crystal(weight-Thicknessficient @ 1064ExamplesFillerpercent)(microns)nm wavelength26(CuFe)(CrFe)2O4354.10.06827(CuFe)(CrFe)2O4540.90.075w/additional 5weight-percenttalc

The polymer composites formed may be used to make circuits having fine electrically conductive pathways. The fine electrically conductive pathways may be formed using an electro-less metal plating step. After light-activating the surface of the composite with a laser beam, for example, the light activated portions are plated to form thin lines, or pathways, on the surface of the polymer compositions or composites.

Without wishing to be held to any particular theory of the present invention, at least in some embodiments of the present invention, it is believed that the amplified light (e.g., laser) substantially, if not completely, volatilizes away the polymeric continuous domain, leaving exposed the discontinuous spinel crystal type domains. The heat treatment and sudden exposure to ambient conditions (of the spinel crystals) caused by the amplified light, appears to prepare the crystals to receive metallization processing.

In the foregoing specification, the invention has been described with reference to specific embodiments. However, one of ordinary skill in the art appreciates that various modifications and changes can be made without departing from the scope of the invention as set forth in the claims below. Accordingly, the specification and figures are to be regarded in an illustrative rather than a restrictive sense and all such modifications are intended to be included within the scope of invention.

Benefits, other advantages, and solutions to problems have been described above with regard to specific embodiments. For example, advantages include the formation of fine line features, the simplification of the manufacturing process of making circuits on boards as compared to a lithographic process of forming copper patterns on substrates, the ability to process reel-to-reel at the laser imaging step, in addition to the plating step, as opposed to a panel-to-panel batch processing method. However, the benefits, advantages, solutions to problems, and any element(s) that may cause any benefit, advantage, or solution to occur or become more pronounced are not to be construed as a critical, required, or essential feature or element of any or all the claims.