This invention concerns films and prepregs including UV curable resins that are useful in the manufacture of flexible PCBs as well as to methods for using the films and prepregs in the manufacture of printed circuit boards.
Currently, standard flex-rigid multilayer manufacturing processes use flexible polyimide sheets to overlay the copper structures and noflow prepregs. Such standard flex-rigid laminates use expensive materials. Moreover, the manufacturing method is very complex and requires multiple manual processing steps.
A prior art method for constructing build-ups for an inner-layer flexible multilayer is shown in
The prior art laminate includes a plated through hole (PTH) (30). The area of the plated through hole in the vicinity of the structured polyamide foil layer creates reliability problems because it requires plasma cleaning. In addition, issues with inadequate metallization of the PTH are common and undesirable barrel cracks can form due to the high thermal expansion of the polyimide and the cover layer in comparison the PTH thermal expansion. Moreover, during the lamination process, little to no pressure is applied to cover layer (14) and polyimide foil layer (10). As a result, PTFE inlays are placed in the stack by hand to increase the stack laminating pressure.
Instead of using the polyamide foil layer (10), a cheaper FR4 material layer can be used instead such as is shown in
One or more of the shortcomings with flexible laminates made with polyimide foil layers that are noted above can be overcome by replacing the polyimide foil layer with a prepreg comprising a partially (b-staged) or fully (c-staged) cured thermally curable resin layer and an adjacent UV curable resin layer wherein the UV curable resin layer has at least one UV light cured resin portion and at least on UV light uncured resin portion.
Another aspect of this invention is a laminate comprising a flexible core having a first planar surface and a second planar surface the flexible core including an optional copper foil layer on one or both of the first and second planar surfaces, a UV curable resin layer having at first planar surface associated with one of the planar surfaces of the flexible core wherein the UV curable resin layer has at least one UV light cured resin portion and at least on UV light uncured resin portion and a thermally cured resin layer adhered to a second planar surface of the UV curable resin layer.
Yet another aspect of this invention are methods for manufacturing a flexible inner-layer that include the steps of:
The present invention relates to the use of special prepregs to replace the flexible polyimide sheets currently used in some flexible printed circuit board manufacturing processes. Laminates and printed circuit boards made with the prepregs of this invention suffer from fewer reliability problems such as barrel cracks in PTH's. In addition, no special plasma cleaning/desmearing steps are necessary.
Referring now to the Figures, there is shown in
Any UV curable resin (or photopolymer) that is capable of becoming at least partially liquid and flowable under normal printed circuit board laminating conditions may be used. Examples of useful UV curable resins include, but are not limited to Ultraviolet (UV) and electron beam (EB) energy-cured materials such as urethanes acrylates, polyester acrylates, amino acrylates and epoxy acrylates. In addition, the UV curable materials may include photoinitiators and additives that enhance the performance of the pre and post cured materials.
The properties of a photocured material, such as flexibility, adhesion, and chemical resistance can be provided by functionalized oligomers present in the photocurable composite. As noted above, oligomer photopolymers are typically epoxides, urethanes, polyethers, or polyesters, each of which provides specific properties to the resulting material. Each of these oligomers is typically functionalized by an acrylate. An example shown below is an epoxy oligomer that has been functionalized by acrylic acid. Acrylated epoxies are useful as coatings on metallic substrates, and result in glossy hard coatings.
Acrylated urethane oligomers are typically abrasion resistant, tough, and flexible making ideal coatings for floors, paper, printing plates, and packaging materials. Acrylated polyethers and polyesters result in very hard solvent resistant films, however, polyethers are prone to UV degradation and therefore are rarely used in UV curable material. Often formulations are composed of several types of oligomers to achieve the desirable properties for the material.
As noted above, the prepreg (100) will include a thermally curable resin layer (104). This layer will typically have a thickness of from about 5 μm to about 100 μm and more preferably about 30-60 μm.
The thermally curable resin layers may be made from resins, resin systems or mixtures of resins that are commonly used in the manufacture of printed circuit boards. The resin(s) will typically be a thermoset or thermoplastic resin. Non-limiting examples of useful resins include epoxy resins, cyanurate resins, bismaleimide resins, polyimide resins, phenolic resins, furan resins, xylene formaldehyde resins, ketone formaldehyde resins, urea resins, melamine resins, aniline resins, alkyd resins, unsaturated polyester resins, diallyl phthalate resins, triallyl cyanurate resins, triazine resins, polyurethane resins, silicone resins and any combination or mixture thereof.
In one aspect of this invention, the resin is or includes an epoxy resin. Some examples of useful epoxy resins include phenol type epoxy resins such as those based on the diglycidyl ether of bisphenol A, on polyglycidyl ethers of phenol-formaldehyde novolac or cresol-formaldehyde novolac, on the triglycidyl ether of tris(p-hydroxyphenol)methane, or on the tetraglycidyl ether of tetraphenylethane; amine types such as those based on tetraglycidyl-methylenedianiline or on the triglycidyl ether of p-aminoglycol; cycloaliphatic types such as those based on 3,4-epoxycyclohexylmethyl-3,4-epoxycyclohexane carboxylate. The term “epoxy resin” also stands for reaction products of compounds containing an excess of epoxy (for instance, of the aforementioned types) and aromatic dihydroxy compounds. These compounds may be halogen-substituted. One class of useful epoxy-resins are those that are derivatives of bisphenol A, particularly FR-4. FR-4 is made by an advancing reaction of an excess of bisphenol A diglycidyl ether with tetrabromobisphenol A. Mixtures of epoxy resins with bismaleimide resin, cyanate resin and/or bismaleimide triazine resin can also be applied.
The resin compositions, in addition to a base resin will typically include initiators or catalysts, one or more optional flame retardants and solvents. The flame retardant may be any flame retardant material that is known to be useful in resin compositions used to manufacture prepregs and laminates use to manufacture printed circuit boards. The flame retardant(s) may contain halogens or they may be halogen free. Alternatively, or in addition, the resins may include halogens such as bromine in their backbone structure to impart the cured resin with flame retardant properties.
The resin compositions may also include polymerization initiators or catalysts. Examples of some useful initiators or catalysts include, but are not limited to peroxide or azo-type polymerization initiators (catalysts). In general, the initiators/catalysts chosen may be any compound that is known to be useful in resin synthesis or curing whether or not it performs one of these functions.
The resin compositions will include one or more solvents which are typically used to solubilize the appropriate resin composition ingredients and/or to control resin viscosity and/or in order to maintain the resin ingredients in a suspended dispersion. Any solvent known by one of skill in the art to be useful in conjunction with thermosetting resin systems can be used. Particularly useful solvents include methylethylketone (MEK), toluene, dimethylformamide (DMF), or mixtures thereof. As noted below, the resin compositions are used to manufacture prepregs and laminates. During the manufacturing process, the reinforcing materials are impregnated with or otherwise associated with the resin compositions and some or most of the solvent is removed from the resin compositions to form the prepregs and laminates. Thus, when resin composition or laminate weight percent amounts are listed herein, they are reported on a dry-solvent free-basis unless otherwise noted.
The resin compositions may include a variety of other optional ingredients including fillers, tougheners, adhesion promoters, defoaming agents, leveling agents, dyes, and pigments. For example, a fluorescent dye can be added to the resin composition in a trace amount to cause a laminate prepared therefrom to fluoresce when exposed to UV light in a board shop's optical inspection equipment. Other optional ingredients known by persons of skill in the art to be useful in resins that are used to manufacture printed circuit board laminates may also be included in the resin compositions of this invention.
The partially UV cured prepreg resulting from the UV light exposure step is shown in
Prepregs and Laminates
The thermosetting resins and UV curable resins described above are useful for preparing prepregs shown in side-view in
In another process for manufacturing prepregs, thermosetting resins are premixed in a mixing vessel under ambient temperature and pressure. The viscosity of the pre-mix can be adjusted by adding or removing solvent from the resin. The thermosetting resin (varnish) mix can be used to manufacture unreinforced prepreg sheets and it can also be applied in a thin layer to a Cu foil substrate (RCC—resin coated Cu) using slot-die or other related coating techniques. Thus, it is possible that prepregs used in this invention can include one partially cured thermally curable resin layer having a copper foil on one surface of the sheet. If necessary some or all of the copper foil sheet can be removed to expose the underlying UV curable resin to a UV light source. Indeed, the copper layer can be used as the mask layer and portions of the copper layer can be removed to form UV light transparent portions of the prepreg.
The term “UV curable resin” is used herein to refer to a type of resin—a resin that becomes cured upon exposure to UV light. The term is not intended to indicate the degree of cure of the resin-cured vs. uncured.
The foregoing description of the specific embodiments will reveal the general nature of the disclosure so others can, by applying current knowledge, readily modify and/or adapt for various applications such specific embodiments without departing from the generic concept, and therefore such adaptations and modifications are intended to be comprehended within the meaning and range of equivalents of the disclosed embodiments. It is to be understood that the phraseology or terminology herein is for the purpose of description and not of limitation.
This is a divisional of U.S. patent application Ser. No. 14/838,098 filed on Aug. 27, 2015 which is a continuation of PCT/US2015/38453 filed on Jun. 30, 2015, which claims priority to U.S. provisional application No. 62/019,598, filed on Jul. 1, 2014, the specifications of each of which are incorporated herein by reference.
Number | Name | Date | Kind |
---|---|---|---|
4056421 | Jarvis | Nov 1977 | A |
4628022 | Ors et al. | Dec 1986 | A |
4751146 | Maeda et al. | Jun 1988 | A |
5142448 | Kober | Aug 1992 | A |
5144742 | Lucas et al. | Aug 1992 | A |
5144534 | Kober | Sep 1992 | A |
5175047 | McKenney et al. | Dec 1992 | A |
5263248 | Kiyota et al. | Nov 1993 | A |
5328752 | Miyazato | Jul 1994 | A |
6074803 | McGrath | Jun 2000 | A |
6558975 | Sugino et al. | May 2003 | B2 |
6896760 | Connell et al. | May 2005 | B1 |
7508081 | Matsumura et al. | Mar 2009 | B2 |
8093502 | Mikado et al. | Jan 2012 | B2 |
9764532 | Schonholz | Sep 2017 | B2 |
20010010303 | Caron et al. | Aug 2001 | A1 |
20040135293 | Umeki | Jul 2004 | A1 |
20080099134 | Tadakuma | May 2008 | A1 |
20100051325 | Sato et al. | Mar 2010 | A1 |
20100059262 | Weidinger et al. | Mar 2010 | A1 |
20110014419 | Simmons et al. | Jan 2011 | A1 |
20110018127 | Lee | Jan 2011 | A1 |
20110272177 | Weichslberger et al. | Nov 2011 | A1 |
20120228005 | Chisaka | Sep 2012 | A1 |
20130220535 | Lee et al. | Aug 2013 | A1 |
20150334825 | Bahl et al. | Nov 2015 | A1 |
20160007482 | Schonholz | Jan 2016 | A1 |
Number | Date | Country |
---|---|---|
102 555 652 | Jul 2012 | CN |
4206746 | Jun 1993 | DE |
2467003 | Dec 2011 | EP |
03062591 | Mar 1991 | JP |
03064994 | Mar 1991 | JP |
03141693 | Jun 1991 | JP |
03141694 | Jun 1991 | JP |
05327209 | Dec 1993 | JP |
06204663 | Dec 1994 | JP |
06338663 | Dec 1994 | JP |
07212035 | Aug 1995 | JP |
10022645 | Jan 1998 | JP |
2001127410 | May 2001 | JP |
2004087701 | Mar 2004 | JP |
2005123468 | May 2005 | JP |
2006080212 | Mar 2006 | JP |
2006093647 | Apr 2006 | JP |
2006173188 | Jun 2006 | JP |
2008034433 | Feb 2008 | JP |
2009290193 | Dec 2009 | JP |
WO 9311652 | Jun 1993 | WO |
WO 2009041510 | Apr 2009 | WO |
WO 2009069683 | Apr 2009 | WO |
Entry |
---|
English Abstract for JP 03064994 A, Mar. 1991. |
Machine translation of JP 2006093647 A, Apr. 2006. |
Machine translation of EP 2467003 A2, Jun. 2012. |
English translation for JP 03141694 A, Jun. 1991. |
English abstract of JP 03141694 A, Jun. 1991. |
Number | Date | Country | |
---|---|---|---|
20180200992 A1 | Jul 2018 | US |
Number | Date | Country | |
---|---|---|---|
62019598 | Jul 2014 | US |
Number | Date | Country | |
---|---|---|---|
Parent | 14838098 | Aug 2015 | US |
Child | 15693001 | US |
Number | Date | Country | |
---|---|---|---|
Parent | PCT/US2015/038453 | Jun 2015 | US |
Child | 14838098 | US |