The present invention is related to a film capacitor comprising a conductor, preferably a metal, on a biaxially oriented polypropylene film (BOPP) wherein the BOPP is a fluorinated biaxially oriented polypropylene film (FBOPP).
Film capacitors have been widely used throughout the electronics industry. A film capacitor comprises a polymer film, which functions as a dielectric, with a metal coated on at least one side of the film. The film is then typically layered such that the conductive coatings of adjacent layers are separated by a single layer of film as known in the art.
There has been a long standing, and increasing demand, for capacitors with higher capacitance suitable for use in higher temperature environments. Film capacitors are suitable for higher capacitance, however, the film is susceptible to damage at high temperatures, especially, if polypropylene is utilized as the dielectric film.
BOPP is the material of choice for film capacitors, particularly, in automotive applications, due to its low dissipation factor, high dielectric strength and high self-healing ability. The use of BOPP as the dielectric in a film capacitor has been limited by the low operational temperature. Typically employed high temperature materials are generally electrically inferior to BOPP due to inferior dielectric characteristics and the lack of availability in the correct thickness. Provided herein is a method for modifying BOPP film that can increase its operational temperature. The process is suitable for use with films of desired thickness thereby circumventing the difficulties related to biaxial stretching of high temperature materials.
Polypropylene based dielectric films have therefore never been considered suitable for use in high temperature applications. The present invention provides a fluorinated biaxially stretched polypropylene film suitable for use in higher temperature applications.
The present invention relates to a film capacitor suitable for use in higher temperature applications.
More specifically, the present invention is related to a film capacitor comprising a conductive, preferably metal, coating on at least one side of a fluorinated biaxially oriented polypropylene (FBOPP) film.
Even more specifically, the present invention is related to a film capacitor comprising a layered structure wherein at least one layer of the layered structure comprises a fluorinated biaxially oriented polypropylene film comprising a conductive, preferably metal, coating on at least one side of the fluorinated biaxially stretched polypropylene film.
Yet another embodiment is provided in a film capacitor comprising a first fluorinated biaxially oriented polypropylene film and a conductive coating on at least one side of the first fluorinated biaxially oriented polypropylene film.
Yet another embodiment is provided in a process for forming a film capacitor comprising:
The present invention is related to improved film capacitors and more specifically to improved film capacitors based on biaxially oriented polypropylene film (BOPP) as the dielectric wherein the BOPP is fluorinated BOPP (FBOPP).
The invention will be described with reference to the figures which form an integral, non-limiting component of the disclosure. Throughout the various figures similar elements will be number accordingly.
An embodiment of the invention will be described with reference to
An embodiment of the invention will be described with reference to
The cross-sectional size of the FBOPP is not particularly limited and chosen to meet the design limitations including capacitance as a function of available space.
Biaxial stretching to form a biaxially oriented film is a well known technique wherein a roll of film is stretched in a machine direction (MD), which is perpendicular to the width of the film, and transverse direction (TD), which is parallel to the width of the film. Machine direction and transverse direction can be done simultaneously or sequentially. In some instances biaxial stretching is done while the film is in a partially molten state. Biaxial stretching can be accomplished by any technique known in the art such as rolling, uniaxial compression, tenter-frame stretching and the like. Biaxial stretching alters the crystallinity of the polymer thereby altering the properties relative to as-cast material. Biaxial stretched polypropylene is widely available commercially in a variety of suitable thicknesses and therefore further explanation of the process is not warranted herein. Biaxial stretched fluorinated polypropylene with a thickness of less than 6 μm is preferred due to commercial availability.
The conductive layer material is any material which can be coated onto FBOPP to provide a conductive coating and act as the conductor of the capacitor. Metals, carbon and combinations thereof are particularly preferred. Particlarly preferred conductive coatings comprise aluminum, copper, zinc, gold, silver and combinations thereof. The conductive layer is applied by any technique known in the art such as vapor deposition, thermal evaporation, PVD, coating, spraying and the like. The conductive coating is typically applied to a thickness of at least 10 nm to no more than 200 nm.
The operational temperature of the capacitor is significantly improved by fluorination of BOPP to form an FBOPP dielectric film. Direct fluorination of BOPP allows for an increase in operational temperature of the film itself and of the film capacitors made therewith.
The BOPP is preferably fluorinated by a direct fluorination method wherein the film is directly exposed to fluorine gas at a temperature of between about 20° C. and about 150° C. and a fluorine partial pressure of between about 0.01 Bar to about 1.0 Bar. Below about 20° C. insufficient fluorination occurs and above about 150° C. the integrity of the BOPP is compromised prior to adequate fluorination. The fluorination temperature is preferably set initially within a range of about 20° C. to about 40° C. and then increased to a temperature within a range of from about 70° C. to about 100° C. Flourination can be done in the presence of UV activation. It is preferable to maintain the atmosphere and increase the temperature. The atmosphere may also be altered during treatment, however, this is not preferred due to manufacturing conveniences.
A representative example was prepared by an initial treatment for about 24 hour at 25° C. in an atmosphere comprising about 0.1 Bar fluorine and about 0.9 Bar nitrogen. The initial treatment was followed by a 24 hour treatment at about 80° C. in the same atmosphere for convenience. The samples were analyzed by Energy Dispersive X-ray Spectroscopy (EDX). The results are presented in Table 1 wherein the percentage of carbon and fluorine are reported relative to the total concentration of carbon and fluorine in the sample. Other elements are not reported.
As indicated in Table 1, the mean F concentration is approximately 59% of the mean C concentration which corresponds to 29.2% of the H groups being substituted by F which is therefore referred to as about 30% fluorination. No fluorination would be referred to as 0% fluorination, replacing about half of the hydrogens with fluorine would be referred to as 50% fluorination, etc. For the purposes of the instant invention FBOPP is defined as a fluorinated biaxially oriented polypropylene film wherein at least a portion of the hydrogens of the polypropylene polymer are replaced with fluorine. It is preferable that the FBOPP be at least 5% fluorinated. More preferably the FBOPP is at least 10% fluorinated. More preferably, the FBOPP is at least 20%. Most preferably the FBOPP is at least 25% fluorinated. The theoretical maximum for fluorination is 100% wherein all hydrogens are replace with fluorine.
The increase in the operational temperature of the FBOPP, relative to BOPP, prior to coating with a conductor or metal was demonstrated by Differential Scanning Colorimetry (DSC) wherein the crystallization temperature was observed to increase. As evidenced in
Shrinkage of FBOPP was improved over BOPP preconditioned at 80° C. for 24 hours, to exclude thermal-only effect, and the improvement is evident in both machine direction (MD) and transverse direction (TD). Shrinkage improvement is also evident at visual inspection wherein the fluorinated samples do not visually show warpage.
The invention has been described with reference to the preferred embodiments without limit thereto. Additional embodiments and improvements may be realized which are not specifically set forth herein but which are within the scope of the invention as more specifically set forth in the claims appended hereto.
The present invention claims priority to pending U.S. Provisional Patent Application No. 62/537,671 filed Jul. 27, 2017 which is incorporated herein by reference.
Number | Date | Country | |
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62537671 | Jul 2017 | US |