JP5680238B2 - Flame retardant biaxially oriented polyester film - Google Patents

Description

  The present invention relates to a biaxially oriented polyester film having flame retardancy, and more specifically, it has excellent flame retardancy and also has hydrolysis resistance superior to conventional flame retardant polyester films, and a metal layer, The present invention relates to a flame retardant biaxially oriented polyester film that exhibits high flame retardancy even when used by bonding.

  Polyester films, especially biaxially stretched films of polyethylene terephthalate and polyethylene naphthalate, have excellent mechanical properties, heat resistance, and chemical resistance, so magnetic tape, photographic film, packaging film, film for electronic parts, electrical insulation It is widely used as a material for films, metal laminate films, protective films and the like.

In recent years, with the enforcement of the Product Liability Act, there has been a strong demand for flame retardant resin to ensure fire safety.
Halogen-based flame retardants such as organic halogen compounds and halogen-containing organophosphorus compounds that have been used in the past have a high flame-retardant effect, but halogen is liberated during molding and processing, generating corrosive hydrogen halide gas, It has been pointed out that it may corrode molding and processing equipment and may worsen the working environment. Further, it has been pointed out that the flame retardant may generate a gas such as hydrogen halide during combustion such as a fire. Therefore, in recent years, there has been a strong demand for using a flame retardant containing no halogen in place of the halogen flame retardant.
Various phosphorus compounds have been studied as one of flame retardant methods using a flame retardant that does not contain a halogen. For example, flame retardant methods using a phosphoric acid ester compound bleed when added in a large amount to polyester. Out sometimes increased or the melting point decreased.

  In addition, as one of the flame retardant methods for polyester resins, a method of copolymerizing a phosphorus compound with polyester has been studied. For example, Japanese Patent Application Laid-Open No. 2007-9111 (Patent Document 1) discloses a carboxyphosphinic acid component. Among these, it is disclosed that by using a specific carboxyphosphinic acid component, high flame retardancy can be imparted to polyethylene-2,6-naphthalenedicarboxylate in a small amount without using another phosphorus compound. However, the laminated film having a layer containing a carboxyphosphinic acid compound as disclosed in Patent Document 1 exhibits high flame retardancy in the state of the film, but the flame retardancy after processing into a flat cable or the like is used. The flame retardancy of the film may not be reproduced.

  As other phosphorus flame retardants, for example, JP 2009-179037 A (Patent Document 2) and JP 2010-89334 A (Patent Document 3) include phosphoric acid derivatives of inorganic metals such as phosphinic acid metal salts. A laminated film in which a flame retardant layer containing a polyester film is laminated has been proposed. However, the proposed laminated film is a technology that provides a flame retardant layer using a flame retardant and a curing agent on the substrate film in view of the high flammability due to the void structure inside the film of the porous substrate film. there were. Japanese Patent Application Laid-Open No. 2010-229390 (Patent Document 4) describes a composition containing a phosphoric acid derivative of an inorganic metal and a flame-retardant coated electric wire, but it is a technique for making a thermoplastic elastomer resin flame-retardant. In addition, since the thermoplastic elastomer resin is a resin having a high elongation, a decrease in physical properties due to the addition of the flame retardant is not a problem.

  In this way, the polyester base layer itself such as polyethylene terephthalate and polyethylene naphthalate is made flame retardant with a phosphorus-based flame retardant, and further bonded with a metal layer without lowering the hydrolysis resistance due to these flame retardants. When used, a flame-retardant biaxially oriented polyester film that exhibits the same high flame resistance as the film has not yet been proposed.

Japanese Patent Laid-Open No. 2007-9111 JP 2009-179037 A JP 2010-89334 A JP 2010-229390 A

The object of the present invention is to eliminate the problems of the prior art, flame-retard the polyester base layer itself such as polyalkylene terephthalate and polyalkylene naphthalate with a phosphorus-based flame retardant, and further reduce the hydrolysis resistance due to these flame retardants. An object of the present invention is to provide a flame retardant biaxially oriented polyester film in which is suppressed.
The second object of the present invention is to make the polyester base layer itself flame retardant with a phosphorus-based flame retardant, and further to suppress the degradation of hydrolysis resistance by these flame retardants, and at the same time, flame retardancy with excellent reflectance characteristics. The object is to provide a biaxially oriented polyester film.
The third object of the present invention is to use a polyester base layer itself as a flame retardant with a phosphorus-based flame retardant, and further suppress degradation in hydrolysis resistance due to these flame retardants, and is particularly used by being laminated with a metal layer. Another object of the present invention is to provide a flame retardant biaxially oriented polyester film laminate that exhibits high flame retardancy similar to that of the flame retardant biaxially oriented polyester film itself.

As a result of intensive investigations to solve the above problems, the present inventors have used other phosphinic acid metal salts as conventional flame retardants in polyester films such as polyethylene terephthalate and polyethylene naphthalate. It has been found that the hydrolysis resistance of the polyester is not impaired even when a large amount of the phosphorus component is added compared to the system component or the copolymer type phosphorus component.
Based on this knowledge, since there is less influence on physical properties of these polyesters compared to conventional phosphorus-based flame retardants, a large amount of flame retardant components can be added to the polyester base layer. It has been found that a flame retardant biaxially oriented polyester film having both hydrolysis resistance and the present invention has been completed.

（式中、Ｒ^１、Ｒ^２は水素、炭素数１〜６のアルキル基および／またはアリール基であり、Ｍは金属、ｍはＭの価数をそれぞれ表す）

（式中、Ｒ^３、Ｒ^４は水素、炭素数１〜６のアルキル基および／またはアリール基、Ｒ^５は炭素数１〜６のアルキレン基または炭素数６〜１０のアリーレン基、アルキルアリーレン基もしくはアリールアルキレン基であり、Ｍは金属、ｎはＭの価数をそれぞれ表す）
該難燃性二軸配向ポリエステルフィルムと金属層とが積層された難燃性二軸配向ポリエステルフィルム積層体（項１）によって達成される。 An object of the present invention is a flame retardant biaxially oriented polyester film comprising a flame燃基material layer, flame燃基material layer of 94% by weight of polyethylene terephthalate or polyethylene naphthalate based on the weight of the layer More than 98% by weight and a phosphinic acid salt represented by the following formula (1) or a diphosphinic acid salt represented by the formula (2): The average particle diameter of the diphosphinate is 1 μm or more and 5 μm or less, and the average reflectance of the polyester film at a wavelength of 400 to 700 nm is 70% or more and less than 75%,

(Wherein R ¹ and R ² are hydrogen, an alkyl group having 1 to 6 carbon atoms and / or an aryl group, M is a metal, and m is a valence of M)

Wherein R ³ and R ⁴ are hydrogen, an alkyl group having 1 to 6 carbon atoms and / or an aryl group, R ⁵ is an alkylene group having 1 to 6 carbon atoms, an arylene group having 6 to 10 carbon atoms, and an alkylarylene group. Or an arylalkylene group, M represents a metal, and n represents a valence of M.)
This is achieved by a flame retardant biaxially oriented polyester film laminate (Item 1) in which the flame retardant biaxially oriented polyester film and a metal layer are laminated .

  The flame-retardant biaxially oriented polyester film of the present invention has high flame retardancy without reducing the hydrolysis resistance of polyester such as polyalkylene terephthalate or polyalkylene naphthalate, such as a flexible printed circuit board, It can be suitably used for a flat cable, a solar battery back sheet or a reflector.

The present invention will be described in detail below.
<Flame retardant biaxially oriented polyester film>
The flame retardant biaxially oriented polyester film of the present invention is a flame retardant biaxially oriented polyester film including a flame retardant substrate layer, and the flame retardant substrate layer is a polyalkylene terephthalate or poly based on the weight of the layer. Contains 94% by weight or more and 98% by weight or less of alkylene naphthalate, and 2% by weight or more and less than 6% by weight of a phosphinic acid salt represented by the following formula (1) or a diphosphinic acid salt represented by the following formula (2) And the average particle size of the phosphinate or diphosphinate is 1 μm or more and 5 μm or less, and the average reflectance of the polyester film at a wavelength of 400 to 700 nm is 70% or more and less than 75%. It is an axially oriented polyester film.

（式中、Ｒ^１、Ｒ^２は水素、炭素数１〜６のアルキル基および／またはアリール基であり、Ｍは金属、ｍはＭの価数をそれぞれ表す）

(Wherein R ¹ and R ² are hydrogen, an alkyl group having 1 to 6 carbon atoms and / or an aryl group, M is a metal, and m is a valence of M)

（式中、Ｒ^３、Ｒ^４は水素、炭素数１〜６のアルキル基および／またはアリール基、Ｒ^５は炭素数１〜６のアルキレン基または炭素数６〜１０のアリーレン基、アルキルアリーレン基もしくはアリールアルキレン基であり、Ｍは金属、ｎはＭの価数をそれぞれ表す）

Wherein R ³ and R ⁴ are hydrogen, an alkyl group having 1 to 6 carbon atoms and / or an aryl group, R ⁵ is an alkylene group having 1 to 6 carbon atoms, an arylene group having 6 to 10 carbon atoms, and an alkylarylene group. Or an arylalkylene group, M represents a metal, and n represents a valence of M.)

[Flame Retardant Base Layer]
The flame retardant substrate layer of the present invention contains polyalkylene terephthalate or polyalkylene naphthalate as a polymer component in the range of more than 94% by weight and 98% by weight or less with respect to the flame retardant substrate layer. As a component, the phosphinic acid salt represented by the above formula (1) or the diphosphinic acid salt represented by the formula (2) is contained in a range of 2 wt% or more and less than 6 wt% with respect to the flame retardant substrate layer. .

(polyester)
Examples of the polyalkylene terephthalate in the present invention include polyethylene terephthalate, polytrimethylene terephthalate, and polybutylene terephthalate. Among these, polyethylene terephthalate is preferable. Examples of the polyalkylene naphthalate in the present invention include polyethylene naphthalate, polytrimethylene naphthalate, and polybutylene naphthalate. Among these, polyethylene naphthalate is preferable, and polyethylene-2,6-naphthalate is more preferable.

The lower limit of the content of these polyesters is preferably 65% by weight based on the weight of the flame retardant substrate layer, more preferably 70% by weight, still more preferably 75% by weight, 80% by weight is particularly preferred.
Further, the upper limit of the content of these polyesters is preferably 96% by weight, more preferably 94% by weight, still more preferably 90% by weight, particularly preferably in relation to the content of the flame retardant component described later. 85% by weight.
If the content of these polyesters is less than the lower limit, the film-forming property will be poor. On the other hand, if the content of these polyesters exceeds the upper limit, the content of flame retardant components will be relatively small and sufficient flame retardancy will be achieved. Does not develop.

  The polyalkylene terephthalate or polyalkylene naphthalate of the present invention may be a copolymer having a component other than the main component (hereinafter sometimes referred to as a copolymer component) within a range not impairing the object of the present invention, Preferably, the copolymerization component can be used in a range of less than 25 mol% based on the number of moles of all repeating units of these polyesters, more preferably 20 mol% or less, and even more preferably 15 mol% or less.

Examples of the copolymer component include oxalic acid, adipic acid, phthalic acid, sebacic acid, dodecanedicarboxylic acid, isophthalic acid, terephthalic acid, 1,4-cyclohexanedicarboxylic acid, 4,4′-diphenyldicarboxylic acid, phenylindanedicarboxylic acid, 2,6-naphthalenedicarboxylic acid, 2,7-naphthalenedicarboxylic acid, tetralin dicarboxylic acid, decalin dicarboxylic acid, dicarboxylic acid such as diphenyl ether dicarboxylic acid, oxycarboxylic acid such as p-oxybenzoic acid, p-oxyethoxybenzoic acid, Or ethylene glycol, trimethylene glycol, tetramethylene glycol, hexamethylene glycol, cyclohexanedimethanol, neopentyl glycol, ethylene oxide adduct of bisphenolsulfone, bisphenol Examples include diols such as ethylene oxide adduct of A, diethylene glycol, and polyethylene oxide glycol, and components other than the main components can be preferably used. These copolymer components may be used alone or in combination of two or more.
These copolymer components may be copolymerized as monomer components, or may be copolymerized by transesterification with other polyesters.

In addition, the polyalkylene terephthalate or polyalkylene naphthalate of the present invention may be a blend of at least two kinds of polyesters or a blend with a thermoplastic resin other than polyester as long as the object of the present invention is not impaired. These other components can be used in a range of 20% by weight or less, more preferably 15% by weight or less, and still more preferably 10% by weight or less, based on the weight of the flame retardant substrate layer. Examples of thermoplastic resins other than polyester include polyolefin resins, polystyrene resins, polyimide resins, and the like.
The intrinsic viscosity of these polyesters is preferably 0.4 dl / g or more and 1.5 dl / g or less, more preferably 0.5 dl / g, measured at 25 ° C. using o-chlorophenol as a solvent. It is preferable that it is 1.2 dl / g or more.

(Flame retardant component)
The present invention uses a phosphinate represented by the following formula (1) or a diphosphinate represented by the formula (2) as a flame retardant component. Hereinafter, these may be collectively referred to as phosphinates.

（式中、Ｒ^１、Ｒ^２は水素、炭素数１〜６のアルキル基および／またはアリール基であり、Ｍは金属、ｍはＭの価数をそれぞれ表す）

(Wherein R ¹ and R ² are hydrogen, an alkyl group having 1 to 6 carbon atoms and / or an aryl group, M is a metal, and m is a valence of M)

（式中、Ｒ^３、Ｒ^４は水素、炭素数１〜６のアルキル基および／またはアリール基、Ｒ^５は炭素数１〜６のアルキレン基または炭素数６〜１０のアリーレン基、アルキルアリーレン基もしくはアリールアルキレン基であり、Ｍは金属、ｎはＭの価数をそれぞれ表す）

Wherein R ³ and R ⁴ are hydrogen, an alkyl group having 1 to 6 carbon atoms and / or an aryl group, R ⁵ is an alkylene group having 1 to 6 carbon atoms, an arylene group having 6 to 10 carbon atoms, and an alkylarylene group. Or an arylalkylene group, M represents a metal, and n represents a valence of M.)

The phosphinic acid salt is a compound also referred to as a phosphinic acid metal salt. As R ¹ and R ² , hydrogen, methyl group, ethyl group, n-propyl group, isopropyl group, n-butyl group, t-butyl group, Examples include a pentyl group, a hexyl group, and a phenyl group. Examples of M include aluminum, magnesium, and calcium, and the valence m is an integer of 2 to 4.
Specifically, calcium dimethylphosphinate, calcium methylethylphosphinate, calcium diethylphosphinate, calcium phenylphosphinate, calcium biphenylphosphinate, magnesium dimethylphosphinate, magnesium methylethylphosphinate, magnesium diethylphosphinate, phenylphosphinic acid Examples thereof include magnesium, magnesium biphenylphosphinate, aluminum dimethylphosphinate, aluminum methylethylphosphinate, aluminum diethylphosphinate, aluminum phenylphosphinate, and aluminum biphenylphosphinate.

Moreover, among diphosphinic acid salts, as R ³ and R ⁴ , hydrogen, methyl group, ethyl group, n-propyl group, isopropyl group, n-butyl group, t-butyl group, pentyl group, hexyl group, phenyl group, There are exemplified, methylene group as R ^5, ethylene group, propylene group, butylene group, pentylene group, hexylene group, a phenylene group are exemplified. Moreover, aluminum, magnesium, and calcium are illustrated as M, and the valence n is an integer of 2-4.
Examples of the diphosphinic acid salt represented by the formula (2) include alkanebis (phosphinic acid) calcium such as ethane-1,2-bis (phosphinic acid) calcium and alkanebis (alkyl alkyl such as ethane-1,2-bis (methylphosphinic acid) calcium. Phosphinic acid) calcium, alkane bisphosphinic acid magnesium, alkane bis (alkyl phosphinic acid) magnesium, alkane bis phosphinic acid aluminum, alkane bis (alkyl phosphinic acid) aluminum and the like.
Of these phosphinic acid salts, aluminum diethylphosphinate is particularly preferable.

  Since the present invention uses such phosphinates as a flame retardant component, it is less affected by a decrease in physical properties of a high-strength polyester such as polyalkylene terephthalate or polyalkylene naphthalate compared to conventional phosphorus flame retardants. It has a feature that a large amount of flame retardant component can be added to such an extent that it could not be added until now. Therefore, for example, when it is processed into an application used by being laminated with a metal layer, it has a characteristic that high flame retardancy similar to that of the flame-retardant polyester film itself can be obtained.

Moreover, the flame-retardant biaxially oriented polyester film of the present invention contains such phosphinates and is biaxially stretched to exhibit high reflectance characteristics.
The content of such phosphinates is 2% by weight or more and 40% by weight or less based on the weight of the flame retardant base material layer. The lower limit of the content of such phosphinates is preferably 4% by weight, more preferably 6% by weight, still more preferably 10% by weight, and particularly preferably 15% by weight. Moreover, the upper limit of the content of the phosphinate is preferably 35% by weight, more preferably 30% by weight, still more preferably 25% by weight, and particularly preferably 20% by weight. If the content of phosphinates is less than the lower limit, the flame retardancy is not sufficient. On the other hand, if the content of phosphinates exceeds the upper limit, the film-forming property is lowered.

The average particle diameter of such phosphinic acid salts is preferably 0.1 μm or more and 35 μm or less. If the average particle size is less than the lower limit, the handleability during film formation may be reduced. On the other hand, when the average particle diameter exceeds the upper limit, the film strength may decrease or the film may be easily broken.
In addition, since the phosphinic acid salts of the present invention have such an average particle diameter, voids are easily generated at the interface between the phosphinic acid salts and the polyester phase by biaxial stretching, and the reflectance of the obtained biaxially oriented polyester film is high. It exhibits a reflectance characteristic as well as a flame retardant effect. Further, the smaller the average particle diameter, the higher the reflectance tends to be as will be described later.

(Phosphorus atom concentration)
The phosphorus atom concentration in the present invention is preferably 1% by weight or more and 8% by weight or less based on the weight of the flame retardant substrate layer. The lower limit of the phosphorus atom concentration is more preferably 1.5% by weight, further preferably 2.0% by weight, particularly preferably 2.5% by weight, and particularly preferably 3.0% by weight. On the other hand, the upper limit of the phosphorus atom concentration is more preferably 7.0% by weight, and even more preferably 6.5% by weight.
In the present invention, the use of the phosphinic acid salts of the present invention for a high-strength polyester such as polyalkylene terephthalate or polyalkylene naphthalate allows the polyester to be used in comparison with conventional additive-type phosphorus-based components or copolymer-type phosphorus-based components. It is characterized in that the hydrolysis resistance is not impaired. Therefore, it can be added in a large amount to these polyesters, and the concentration of phosphorus atoms in the flame retardant substrate layer can be increased to a level that cannot be obtained with conventional phosphorus-based components.

  On the other hand, when it is going to raise to the phosphorus atom density | concentration exceeding an upper limit, there is too much quantity of the phosphinic acid salt to add, and film film forming property will become scarce. Also, in the range close to the lower limit of the phosphorus atom concentration, that is, in the range close to the content of the conventional phosphorus component, it is higher than other phosphorus components due to the radical trap effect by the metal component constituting the phosphinates. It is considered that flame retardancy is expressed, and has the characteristics that high flame retardance similar to that of the flame retardant polyester film itself is reproduced even when processed for use in a laminate with a metal layer.

(Other additives)
In order to improve the handleability of the film, inert particles or the like may be added to the flame-retardant biaxially oriented polyester film of the present invention within a range not impairing the effects of the invention. Examples of the inert particles include inorganic particles (for example, kaolin, alumina, titanium oxide, calcium carbonate, silicon dioxide) containing the elements of Periodic Tables IIA, IIB, IVA, and IVB, and crosslinked silicone resins. , Particles made of a polymer having high heat resistance such as crosslinked polystyrene and crosslinked acrylic resin particles.
When the inert particles are contained, the average particle diameter of the inert particles is preferably in the range of 0.001 to 5 μm, and may be contained in the range of 0.01 to 10% by weight based on the flame retardant substrate layer. It is preferably 0.05 to 5% by weight, more preferably 0.05 to 3% by weight.
The flame retardant biaxially oriented polyester film of the present invention may further contain additives such as a heat stabilizer, an antioxidant, an ultraviolet absorber, a release agent, a colorant, and an antistatic agent as necessary. It can mix | blend in the range which does not impair the objective.

(Layer thickness)
The thickness of the flame retardant substrate layer in the present invention is preferably 2 μm or more and 200 μm or less. Conventionally, when a flame retardant is attempted by adding a phosphorus-based flame retardant to a polyester base layer, the mechanical properties and hydrolysis resistance of the base layer are reduced. In contrast to the method of laminating another layer containing a flame retardant on the base material layer, rather than making it flame retardant with a flame retardant, the present invention is based on the polyester base material layer having such a thickness. It has the characteristic that a flame retardant can be added.

  The thickness of the flame retardant substrate layer can be adjusted according to the application within the above-described range. For example, in the case of a flat cable application, it is more preferably 2 to 100 μm, further preferably 5 to 75 μm, and particularly preferably 10 to 50 μm. Moreover, in the case of a flexible printed circuit board use, More preferably, it is 2-150 micrometers, More preferably, it is 5-100 micrometers, Especially preferably, it is 10-75 micrometers, In the case of a solar cell backsheet use, More preferably, it is 5-200 micrometers, More preferably, it is 10- In the case of a reflector use, it is more preferably 50 to 200 μm, still more preferably 100 to 200 μm, and particularly preferably 150 to 200 μm.

[Heat seal layer]
The flame retardant biaxially oriented polyester film of the present invention preferably has a heat seal layer on at least one side of the flame retardant substrate layer. Such a heat seal layer may be a layer coated with a heat-sealing adhesive, or may be a layer composed of a polymer having a melting point lower than that of the flame retardant substrate layer.

The heat-seal type adhesive is also called a hot-melt type adhesive, and a known one can be used. For example, the product name “HM326” manufactured by Cemedine Co., Ltd. and the product name “Elfan PH” manufactured by Nippon Matai Co., Ltd. are exemplified.
Moreover, as a layer comprised with a polymer whose melting point is lower than that of the flame retardant substrate layer, for example, a layer using a copolyester is exemplified.
As the main component of the copolymer polyester, a polyester of the type described in the flame retardant substrate layer can be used. Of these, ethylene terephthalate or ethylene naphthalate is preferable. The main component amount of the copolyester is preferably more than 50 mol%, more preferably 60 mol% or more, based on all the repeating units of the polyester constituting the heat seal layer.

Further, the secondary component constituting the copolymer polyester is preferably more than the total copolymerization amount of the polyester of the flame retardant substrate layer and less than 50 mol% based on the total repeating units of the polyester of the heat seal layer. . Such a copolyester has a relatively lower melting point than that of the polyester of the flame retardant base material layer, so that the mating material for bonding the heat seal layer surface of the flame retardant polyester film of the present invention, specifically, a conductor to be described later, etc. Facing the metal layer, etc., and heat-pressing at a temperature higher than the melting point of the heat-seal layer and lower than the melting point of the flame-retardant substrate layer, the heat-seal layer in the molten state is heat-sealed with the counterpart material and bonded. be able to.
Subordinate components constituting the copolymer polyester include isophthalic acid, terephthalic acid, 2,6-naphthalenedicarboxylic acid, 4,4′-diphenyldicarboxylic acid, 2,7-naphthalenedicarboxylic acid, p-oxybenzoic acid and the like. Of the diol components such as dicarboxylic acid components, trimethylene glycol, hexamethylene glycol, neopentyl glycol, and ethylene oxide adducts of bisphenolsulfone, components other than the main component are preferably exemplified.
Such a heat seal layer is preferably provided when used as a flat cable or a solar battery back sheet.

<Hydrolysis resistance>
The flame-retardant biaxially oriented polyester film of the present invention preferably has a polyester film tensile strength retention of 50% or more after being treated in saturated steam at 121 ° C. and 2 atm for 10 hours. Such film tensile strength retention is more preferably 60% or more. Such tensile strength retention is sometimes referred to as the film continuous film forming direction of the polyester film (hereinafter sometimes referred to as the longitudinal direction, the longitudinal direction, and the MD direction) or the orthogonal direction thereof (hereinafter referred to as the width direction, the lateral direction, and the TD direction). It is more preferable that the tensile strength retention rate in at least one direction is satisfied in both directions.
The flame retardant biaxially oriented polyester film of the present invention is excellent in flame retardancy and also has excellent hydrolysis resistance by using the phosphinic acid salts of the present invention as a flame retardant component. A high film tensile strength retention rate can be maintained thereafter.

<Reflectance characteristics of film>
The flame-retardant biaxially oriented polyester film of the present invention has flame retardancy and excellent hydrolysis resistance, and at the same time has high reflection characteristics. Specifically, the average reflectance of the polyester film at a wavelength of 400 to 700 nm is preferably 70% or more and 100% or less, more preferably 75% or more and 100% or less, and particularly preferably 80% or more and 100% or less. It is. By having such a reflectance characteristic, it can be suitably used as a reflector having, for example, flame retardancy and reflection characteristics.

Such reflectance characteristics can be obtained by a method in which a conventional flame retardant reflector uses white particles that increase the reflectance, or a resin that is incompatible with the matrix resin, and further laminates a layer containing a flame retardant. However, in the present invention, the phosphinic acid salts of the present invention are contained in the base material layer, and the void can be efficiently formed by biaxial stretching, and the reflectance is improved while obtaining flame retardancy. is there.
Further, among the phosphinic acid salts of the present invention, the reflectance characteristics can be further improved by using those having an average particle diameter of 1 μm or more and 10 μm or less, and further 1 μm or more and 5 μm or less.

<Film density>
The flame-retardant biaxially oriented polyester film of the present invention also has a feature that the film density is smaller than that of a general polyester film.
Specifically, the film density is preferably 0.7 g / cm ³ or more and 1.3 g / cm ³ or less, more preferably 0.8 g / cm ³ or more and 1.2 g / cm ³ or less, particularly preferably 0. .8g / cm ³ or more 1.1g / cm ³ or less. Such a film density is obtained by generating a void at the interface between the phosphinic acid salts and the polyester phase by biaxially stretching the polyester film using a specific amount of the phosphinic acid salts having the above average particle diameter.

By having such a film density, in addition to improving the above-described reflectance characteristics, a flame-retardant biaxially oriented polyester film having excellent film folding characteristics and punching properties even in a state containing a large amount of phosphinates can be obtained. It is easy to punch into shapes for various uses of the present invention. On the other hand, as the content of phosphinates increases, the density decreases. However, when bending characteristics are required, the lower limit of the density is preferably 0.8 g / cm ³ .
Since the flame-retardant biaxially oriented polyester film of the present invention has excellent bending characteristics as well as flame retardancy and hydrolysis resistance, it is suitably used for flexible printed circuits, flat cables and the like that require flexibility.

<Surface roughness of substrate layer>
The surface roughness Ra of the flame retardant substrate layer of the present invention is preferably from 0.1 μm to 2 μm, more preferably from 0.2 μm to 1.5 μm, and even more preferably from 0.5 μm to 1.5 μm. is there. Such surface roughness can be obtained by using a specific amount of the phosphinic acid salts having the above-mentioned average particle diameter in the base material layer.
Adhesiveness when laminating with other layers through a heat seal layer or adhesive layer is improved due to the rough surface over which the flame retardant substrate layer is applied, and is suitable for applications such as flat cables and solar battery back sheets. Can be used.

<Film production method>
As a method for producing the flame-retardant biaxially oriented polyester film of the present invention, there is a film production method in which the polyester constituting the base material layer is melt-extruded and the solidified and formed sheet is stretched in two directions.
The film-forming method can be manufactured using a known film-forming method. For example, after sufficiently drying a polyester containing a phosphinate, it is melted in an extruder at a temperature of melting point to (melting point + 70) ° C. , Melt extrusion through a T-die, quench the film-like melt on a chill roll (casting drum) to make an unstretched film, and then produce the unstretched film by sequential or simultaneous biaxial stretching and heat setting. Can do. When the film is formed by sequential biaxial stretching, the unstretched film is stretched in the longitudinal direction at 60 to 170 ° C. in a range of 2.3 to 5.5 times, more preferably 2.5 to 5.0 times, and then a stenter. The film is stretched in the range of 2.3 to 5.0 times, more preferably 2.5 to 4.8 times at 80 to 170 ° C. in the transverse direction.
The heat setting is preferably heat setting at a temperature of 180 to 260 ° C., more preferably 190 to 240 ° C. under tension or limited shrinkage, and the heat setting time is preferably 1 to 1000 seconds. In the case of simultaneous biaxial stretching, the above stretching temperature, stretching ratio, heat setting temperature and the like can be applied. Moreover, you may perform a relaxation | loosening process after heat setting.

When a layer composed of a polymer having a melting point lower than that of the flame retardant substrate layer is provided as the heat seal layer, it is supplied to an extruder different from the flame retardant substrate layer and melted at a temperature of melting point to (melting point + 70) ° C. And the method of obtaining the laminated unstretched film by the method of laminating | stacking the molten resin for both layers inside die | dye, for example, the simultaneous lamination extrusion method using a multi-manifold die, is mentioned. As for the subsequent stretching method, the above-described method can be used.
Moreover, when providing the layer which apply | coated the heat-fusion-type adhesive agent as a heat seal layer, the method of apply | coating an adhesive agent on the obtained base material layer is mentioned.

<Flame retardant biaxially oriented polyester film laminate>
The flame retardant biaxially oriented polyester film of the present invention can be used as a flame retardant biaxially oriented polyester film laminate laminated with a metal layer. Here, the metal layer includes a layer formed on a film, a conductor, a certain pattern such as a circuit, and the like.
In laminating the flame retardant biaxially oriented polyester film with the metal layer, it is preferable to laminate the flame retardant biaxially oriented polyester film on the heat seal layer of the flame retardant biaxially oriented polyester film. By laminating with a metal layer via a heat seal layer, a flame-retardant biaxially oriented polyester film laminate can be obtained by a simple method.
Such a flame retardant biaxially oriented polyester film laminate can be suitably used for applications requiring flame retardancy and hydrolysis resistance, and examples thereof include applications such as flat cables and flexible printed circuit boards. Further, it can be used for other applications to be bonded to a metal layer.

(Flat cable)
The flame-retardant biaxially oriented polyester film and the laminate thereof of the present invention can be used as a covering material for flat cables. A flat cable is a cable having a flat shape in which a metal layer in the form of a conductor is covered with an electrically insulating coating material in a sandwich shape.
When creating a flat cable using the flame retardant biaxially oriented polyester film of the present invention, two flame retardant biaxially oriented polyester films having a heat seal layer are used to oppose the heat seal layers, and a plurality of them are interposed therebetween. By arranging the lead wires in parallel at intervals, and then heat-sealing the heat seal layer in a molten state at a temperature range above the melting point of the heat seal layer and below the melting point of the flame retardant substrate layer Can create flame retardant flat cable.
As a conducting wire, a normal conducting wire used for a flat cable can be used, and examples thereof include copper, plated copper, and silver. The conducting wire has a foil shape or a rectangular shape, and is arranged in parallel at a predetermined interval.

The flat cable obtained by using the flame retardant biaxially oriented polyester film laminate of the present invention has a very high flame resistance of the base material layer itself, and is processed into a flat cable application used by being laminated with a metal layer. In this case, high flame retardancy similar to that of the flame retardant biaxially oriented polyester film itself is exhibited, and sufficient hydrolysis resistance is provided, so that it is excellent in long-term durability as a flat cable. In addition, since the flame-retardant biaxially oriented polyester film of the present invention can achieve both flame retardancy and bendability, a highly flexible flame-retardant flat cable can be obtained.
Furthermore, the flame retardant biaxially oriented polyester film of the present invention has an effect that the surface is rough and the adhesiveness with an adhesive layer such as a heat seal layer is enhanced.

(Flexible printed circuit board)
The flame-retardant biaxially oriented polyester film and the laminate thereof of the present invention can be used for a flexible printed circuit board.
When using for such a use, it is preferable that a metal layer is laminated | stacked on one side of a flame-retardant biaxially-oriented polyester film, and it is used as a flexible printed circuit board. A copper foil is illustrated as a metal layer used in this use. There are no particular restrictions on the means for joining and shape of the metal layer, for example, a so-called subtractive method in which a metal layer is laminated on a flame retardant biaxially oriented polyester film, and then the metal layer is subjected to pattern etching. An additive method of plating metal in a pattern on a biaxially oriented polyester film, a stamping foil for bonding a metal layer punched in a pattern to a flame retardant biaxially oriented polyester film, or the like can be used.

The flexible printed circuit board obtained using the flame retardant biaxially oriented polyester film laminate of the present invention has a very high flame resistance of the base material layer itself, and is a flexible printed circuit used by being laminated with a metal layer. Even when processed for substrate use, it exhibits high flame resistance similar to that of the flame retardant biaxially oriented polyester film itself, and also has sufficient hydrolysis resistance, so it can be used for long-term durability as a flexible printed circuit board. Is also excellent. In addition, since the flame-retardant biaxially oriented polyester film of the present invention is also excellent in bendability, it has excellent punchability when processed into a flexible printed circuit board, and furthermore, both flame retardancy and bendability can be achieved. A flexible printed circuit board with high flexibility can be obtained.
Since the flame-retardant biaxially oriented polyester film and the laminate thereof of the present invention are excellent in reflectance characteristics, they can be used as flexible printed circuit boards for LEDs.

(Solar cell)
The flame-retardant biaxially oriented polyester film of the present invention can be used for a back sheet of a solar cell.
The solar cell backsheet obtained using the flame retardant biaxially oriented polyester film of the present invention is excellent in flame retardancy and also has sufficient hydrolysis resistance, thereby improving the long-term durability of the solar cell. be able to.
Moreover, by containing the phosphinic acid salts of the present invention in a film, high whiteness can be obtained, and the film can be used as a back sheet for a solar cell in which whiteness is required.
Furthermore, the flame-retardant biaxially oriented polyester film of the present invention has a rough surface, improves adhesion with EVA used as a filler for solar cells, and can further enhance long-term durability as a solar cell.

(reflector)
The flame-retardant biaxially oriented polyester film of the present invention can be used as various reflectors because it has both high flame retardancy and hydrolysis resistance, as well as high reflectance characteristics. Specifically, a reflecting plate of a liquid crystal display device, a reflecting plate of a lighting device, and the like can be given.
In addition, when used as a reflector for a liquid crystal display device, the surface roughness characteristics of the present invention can reduce sticking to adjacent members and suppress a decrease in reflectance characteristics during long-term use.

  EXAMPLES Hereinafter, although an Example demonstrates this invention in detail, this invention is not limited only to these Examples. Each characteristic value was measured by the following method. Moreover, unless otherwise indicated, the part and% in an Example mean a weight part and weight%, respectively.

(1) Type and content of polyester component
^{By 1} H-NMR measurement and ¹³ C-NMR measurement, a polyester component, a copolymer component, and an amount of each component were specified.

(2) Type of phosphorus component The type of phosphorus component was specified using NMR and EPMA.

(3) Phosphorus atom concentration For the flame retardant substrate layer, the phosphorus atom concentration was calculated from the emission intensity of fluorescent X-rays.

(4) Thickness of each layer The thickness of each layer of the laminated film is determined by embedding a small piece of film in an epoxy resin (trade name “Epomount” manufactured by Refine Tech Co., Ltd.) and embedding using Microtome 2050 manufactured by Reichert-Jung. The whole resin was sliced to a thickness of 50 nm and measured by an accelerating voltage of 100 KV using a transmission electron microscope (LEM-2000).

(5) Hydrolysis resistance A strip-shaped sample cut out of a film 150 mm long × 10 mm wide is suspended with a stainless steel clip in an environmental tester set to 121 ° C., 2 atm, wet saturation mode, and 100% RH. . Thereafter, a sample piece is taken out of the environmental tester after 10 hours and the tensile strength is measured. The longitudinal direction of the film was taken as the measurement direction, the measurement was carried out five times, the average value was determined, and the hydrolysis resistance was evaluated according to the following criteria. As a measuring device, Tensilon UCT-100 type manufactured by Orientec Co., Ltd. was used.
Tensile strength retention rate (%) = (Tensile strength after treatment X / initial tensile strength X ₀ ) × 100
(In the formula, tensile strength X represents the tensile strength after treatment for a predetermined time under the conditions of 121 ° C., 2 atm, and 100% RH, and tensile strength X ₀ represents the initial tensile strength before treatment)
◯: Tensile strength retention after 10 hours is 50% or more ×: Tensile strength retention after 10 hours is less than 50%

(6) Flammability Film samples were evaluated according to the UL-94 VTM method. The sample was cut into 20 cm × 5 cm and left in 23 ± 2 ° C. and 50 ± 5% RH for 48 hours, and then the lower end of the sample was held 10 mm above the burner and held vertically. The bottom end of the sample was indirectly heated for 3 seconds using a Bunsen burner having an inner diameter of 9.5 mm and a flame length of 19 mm as a heating source. Flame retardance was evaluated according to the evaluation standards of VTM-0, VTM-1, and VTM-2, and among the number of measurements of n = 5, the rank having the same number of ranks was set.

(7) Flammability of flat cable A hot melt adhesive (product name “Erphan PH” manufactured by Nippon Matai Co., Ltd.) is applied to one side of the film to a thickness of about 30 μm, and the adhesive is applied. A 35 μm-thick copper foil cut to a width of 3 mm was placed side by side, and two films were bonded together so that the heat seal layers were opposed to each other with the copper foil interposed therebetween, and a flat cable sample was prepared by heat-sealing. .
Moreover, about the film which has the heat-seal layer which consists of a copolyester layer, this heat-seal layer was made to oppose, the 35 micrometer-thick copper foil cut | disconnected to the width | variety of 3 mm was arranged side by side, and it heat-sealed.
In all the heat sealing conditions, the temperature was 140 ° C., the pressure was 2.8 kgf / cm ² , and the heat sealing time was 2 sec.
The produced flat cable sample was evaluated based on the UL-94V method. The sample was cut into 13 mm × 125 mm and left in 50 ± 5% RH for 48 hours, after which the lower end of the sample was held 10 mm above the burner and held vertically. The lower end of the sample was indirectly fired for 10 seconds using a Bunsen burner having an inner diameter of 9.5 mm and a flame length of 19 mm as a heating source. The self-extinguishing property after flame removal was evaluated.
○: Fire extinguishing within 10 seconds after flame release ×: Burning beyond 10 seconds after flame release

(8) Average particle diameter About the cross section of a flame-retardant base material layer, it measured by 3500 times about 20 particles using Hilox digital microscope KH-3000, and calculated | required the average particle diameter from the average value.

(9) Reflectance An integrating sphere was attached to a spectrophotometer (Shimadzu UV-3101PC), and the reflectance of the film flame retardant layer surface was measured over 400 to 700 nm when the BaSO ₄ white plate was taken as 100%. The average reflectance at a film thickness of 50 μm was determined. The reflectance characteristics were evaluated according to the following criteria.
○: 75% or more and 100% or less △: 70% or more and less than 75% ×: Less than 70%

(10) Film density The film was cut into 10 cm × 10 cm, 10 points of thickness were measured with an electric micrometer (Anritsu K-402B), and the average value was taken as the thickness of the film, and then the film weight was measured. Density was calculated.

(11) Surface roughness Ra of the flame retardant substrate layer
Using a stylus type surface roughness meter (SURFCORDER SE-30C) manufactured by Kosaka Laboratory Ltd., the surface of the flame retardant substrate layer is measured under the following conditions, and the calculated centerline average roughness Ra is obtained. Evaluation was performed according to the following evaluation criteria using the average value measured four times.
<Measurement conditions>
Measurement length: 2.5mm
Cut-off: 0.25mm
Measurement environment: room temperature, in the air <Evaluation criteria>
○: 0.2 μm or more and 2 μm or less Δ: 0.1 μm or more and less than 0.2 μm ×: Less than 0.1 μm

(12) Folding resistance Using a MIT folding resistance tester, in accordance with JIS C5016, the number of folding times until the film sample breaks was measured at a bending portion polar radius of 0.38 mm, a load of 10 N, and a folding speed of 175 cpm. Evaluation was made according to the following criteria.
○: 2000 times or more △: 500 times or more and less than 2000 times ×: Less than 500 times

[Reference Example 1]
Polyethylene terephthalate (transesterification catalyst: manganese acetate tetrahydrate, polymerization catalyst: antimony trioxide) having an intrinsic viscosity of 0.60 dl / g and a terminal carboxyl group concentration of 25 equivalents / ton was used as polyester, and aluminum dimethylphosphinate (in Table 1) And a composition containing 15% by weight of phosphor compound A (average particle size 2 μm) based on the weight of the flame retardant substrate layer, dried for 3 hours with a 170 ° C. dryer, and then put into an extruder, melting temperature 280 After melt-kneading at ℃ and extruding from a die slit at 280 ℃, it was cooled and solidified on a casting drum set at a surface temperature of 25 ℃ to prepare an unstretched film.
This unstretched film was led to a roll group heated to 100 ° C., stretched 3.5 times in the longitudinal direction (longitudinal direction), and cooled with a roll group at 25 ° C. Subsequently, both ends of the longitudinally stretched film were guided to a tenter while being held by clips, and stretched in a direction perpendicular to the longitudinal direction (lateral direction) at a magnification of 3.8 times in an atmosphere heated to 120 ° C. Thereafter, heat setting was performed at 230 ° C. in a tenter, and after relaxing by 2% in the width direction at 180 ° C., the film was gradually and gradually cooled to room temperature to obtain a biaxially stretched film having a thickness of 50 μm. The properties of the obtained film are shown in Table 1. The film of this reference example was excellent in flame retardancy and hydrolysis resistance. The film of this example was also excellent in reflectance characteristics and bending characteristics.
Furthermore, the flame resistance was excellent even in the state of the flat cable produced with the copper foil sandwiched therebetween. Moreover, when the peel strength was measured about the adhesiveness of a flame-resistant base material layer and a heat seal layer using the produced flat cable, intensity | strength improved rather than the comparative example 1. FIG.

[Reference Example 2]
A biaxially stretched film having a thickness of 50 μm was obtained by performing the same operation as in Reference Example 1 except that the flame retardant was changed to aluminum diethylphosphinate (indicated as phosphorus compound B in Table 1, average particle diameter 2 μm). The properties of the obtained film are shown in Table 1. The film of this reference example was excellent in flame retardancy, hydrolysis resistance, reflectance characteristics, and bending characteristics. Furthermore, the flame resistance was excellent even in the state of the flat cable produced with the copper foil sandwiched therebetween. Moreover, when the peel strength was measured about the adhesiveness of a flame-resistant base material layer and a heat seal layer using the produced flat cable, intensity | strength improved rather than the comparative example 1. FIG.

[Example 1]
A biaxially stretched film having a thickness of 50 μm was obtained by performing the same operation as in Reference Example 2 except that the content of the flame retardant was changed to 5% by weight. The properties of the obtained film are shown in Table 1. The film of this example was excellent in flame retardancy, hydrolysis resistance, and bending characteristics. Furthermore, the flame resistance was excellent even in the state of the flat cable produced with the copper foil sandwiched therebetween.

[Reference Example 3]
A biaxially stretched film having a thickness of 50 μm was obtained by performing the same operation as in Reference Example 2 except that the content of the flame retardant was changed to 30% by weight. The properties of the obtained film are shown in Table 1. The film of this reference example was excellent in flame retardancy, hydrolysis resistance, and reflectance characteristics. Furthermore, the flame resistance was excellent even in the state of the flat cable produced with the copper foil sandwiched therebetween.

[Reference Example 4]
A biaxially stretched film having a thickness of 50 μm was obtained by performing the same operation as in Reference Example 1 except that the flame retardant was changed to aluminum ethylmethylphosphinate (indicated as phosphorus compound C in Table 1, average particle diameter of 3 μm). The properties of the obtained film are shown in Table 1. The film of this reference example was excellent in flame retardancy, hydrolysis resistance, reflectance characteristics, and bending characteristics. Furthermore, the flame resistance was excellent even in the state of the flat cable produced with the copper foil sandwiched therebetween.

[Reference Example 5]
Reference example except that the flame retardant was changed to aluminum biphenylphosphinate (indicated as phosphorus compound D in Table 1, average particle diameter 3 μm) and the content was changed to 20% by weight based on the weight of the flame retardant substrate layer. The same operation as 1 was performed to obtain a biaxially stretched film having a thickness of 50 μm. The properties of the obtained film are shown in Table 1. The film of this reference example was excellent in flame retardancy, hydrolysis resistance, and reflectance characteristics. Furthermore, the flame resistance was excellent even in the state of the flat cable produced with the copper foil sandwiched therebetween.

[Reference Example 6]
A biaxially stretched film having a thickness of 50 μm was obtained in the same manner as in Reference Example 1 except that the flame retardant was changed to calcium dimethylphosphinate (indicated as phosphorus compound E in Table 1 and average particle diameter of 5 μm). The properties of the obtained film are shown in Table 1. The film of this reference example was excellent in flame retardancy, hydrolysis resistance, reflectance characteristics, and bending characteristics. Furthermore, the flame resistance was excellent even in the state of the flat cable produced with the copper foil sandwiched therebetween.

[Reference Example 7]
A biaxially stretched film having a thickness of 50 μm was obtained by performing the same operation as in Reference Example 1 except that the flame retardant was changed to calcium diethylphosphinate (indicated as phosphorus compound F in Table 1, average particle diameter 5 μm). The properties of the obtained film are shown in Table 1. The film of this reference example was excellent in flame retardancy, hydrolysis resistance, reflectance characteristics, and bending characteristics. Furthermore, the flame resistance was excellent even in the state of the flat cable produced with the copper foil sandwiched therebetween.

[Reference Example 8]
Polyethylene-2,6-naphthalenedicarboxylate (transesterification catalyst: manganese acetate tetrahydrate, polymerization catalyst: antimony trioxide) having an intrinsic viscosity of 0.57 dl / g and a terminal carboxyl group concentration of 25 equivalents / ton as a polyester, A composition containing 15% by weight of aluminum diethylphosphinate (phosphorus compound B) based on the weight of the flame retardant substrate layer is dried with a 180 ° C. dryer for 5 hours and then put into an extruder and melted at a melting temperature of 300 ° C. After kneading and extruding from a die slit at 300 ° C., the film was cooled and solidified on a casting drum set at a surface temperature of 60 ° C. to prepare an unstretched film.
This unstretched film was led to a roll group heated to 140 ° C., stretched 3.5 times in the longitudinal direction (longitudinal direction), and cooled by a roll group at 60 ° C. Subsequently, both ends of the longitudinally stretched film were guided to a tenter while being held by clips, and stretched 3.5 times in a direction (lateral direction) perpendicular to the longitudinal direction in an atmosphere heated to 150 ° C. Thereafter, heat setting was performed at 230 ° C. in a tenter, and after relaxing by 2% in the width direction at 180 ° C., the film was uniformly removed and cooled to room temperature to obtain a biaxially stretched film having a thickness of 50 μm. The properties of the obtained film are shown in Table 1. The film of this reference example was excellent in flame retardancy, hydrolysis resistance, reflectance characteristics, and bending characteristics. Furthermore, the flame resistance was excellent even in the state of the flat cable produced with the copper foil sandwiched therebetween.

[Example 2]
A biaxially stretched film having a thickness of 50 μm was obtained by performing the same operation as in Reference Example 8 except that the content of the flame retardant was changed to 5% by weight. The properties of the obtained film are shown in Table 1. The film of this example was excellent in flame retardancy, hydrolysis resistance, and bending characteristics. Furthermore, the flame resistance was excellent even in the state of the flat cable produced with the copper foil sandwiched therebetween.

[Reference Example 9]
20% by weight of aluminum diethylphosphinate (phosphorus compound B) based on the weight of the flame retardant substrate layer, a composition using polyethylene terephthalate as the polyester was dried with a 170 ° C. dryer for 3 hours and then put into an extruder. The mixture was melt kneaded at a melting temperature of 280 ° C.
On the other hand, isophthalic acid copolymerized polyethylene terephthalate having an intrinsic viscosity of 0.59 dl / g obtained by copolymerizing isophthalic acid with 18 mol% based on all repeating units of polyester of the heat sealing layer for a heat seal layer is dried with a 170 ° C. dryer for 3 hours. Thereafter, it was charged into the other extruder and melted at a melting temperature of 270 ° C.
Each layer was laminated in a melted state (thickness ratio flame retardant substrate layer: heat seal layer = 4: 1), extruded from a die slit while maintaining such a laminated structure, and then set to a surface temperature of 25 ° C. An unstretched film composed of two layers was prepared by cooling and solidifying on a casting drum. This unstretched film was biaxially stretched in the same manner as in Reference Example 1 to obtain a biaxially stretched film having a thickness of 50 μm (a flame retardant substrate layer: 40 μm, a heat seal layer: 10 μm). The properties of the obtained film are shown in Table 1. The film of this reference example was excellent in flame retardancy, hydrolysis resistance, and reflectance characteristics.
Furthermore, even in the state of a flat cable produced by sandwiching a copper foil, it was excellent in flame retardancy.

[Reference Example 10 and Comparative Examples 4 and 5]
A biaxially stretched film having a thickness of 50 μm was obtained by performing the same operation as in Reference Example 2 except that aluminum diethylphosphinate (indicated as phosphorus compound B in Table 1) was changed to the average particle diameter shown in Table 2. It was. The properties of the obtained film are shown in Table 2. The film of this example was excellent in flame retardancy, hydrolysis resistance, and bending characteristics. As for the reflectance characteristics, a higher reflectance was obtained when the average particle diameter of the flame retardant was smaller.
Furthermore, the flame resistance was excellent even in the state of the flat cable produced with the copper foil sandwiched therebetween.

[Comparative Example 1]
A biaxially stretched film having a thickness of 50 μm was obtained by performing the same operation as in Reference Example 1 except that no flame retardant was added. The properties of the obtained film are shown in Table 1. Although the film of this comparative example was excellent in hydrolysis resistance, flame retardance was not sufficient for both the film and the flat cable. Also, the reflectivity was low.

[Comparative Example 2]
A biaxially stretched film having a thickness of 50 μm was obtained in the same manner as in Reference Example 2 except that the content of the flame retardant was changed to 45% by weight. The properties of the obtained film are shown in Table 1. In this comparative example, the film forming property was not sufficient, and a biaxially stretched film could not be obtained.

[Comparative Example 3]
100 parts by weight of dimethyl terephthalate and 60 parts by weight of ethylene glycol were subjected to an ester exchange reaction according to a conventional method using 0.03 parts by weight of manganese acetate tetrahydrate as a transesterification catalyst, and then dispersed in ethylene glycol. 0.4% by weight (based on the weight of the film) of calcium carbonate particles having an average particle diameter of 0.5 μm was added. Next, 10 parts by weight of 2-hydroxyethyl 2-carboxyethylmethylphosphinate (indicated as phosphorus compound G in Table 1) was added, 0.03 part by weight of antimony trioxide was added, and then continuously under high temperature and high vacuum. A polycondensation reaction was performed by a conventional method to obtain a polyester having an intrinsic viscosity of 0.70 dl / g. The obtained polyester is dried for 3 hours with a 170 ° C. dryer, put into an extruder, melted at 260 ° C. and extruded through a die slit, and then cooled and solidified on a casting drum set at a surface temperature of 25 ° C. to be unstretched. A film was created.
This unstretched film was stretched 3.5 times in the longitudinal direction (continuous film-forming direction) at 100 ° C., and then successively biaxially stretched 3.8 times in the transverse direction (width direction) at 130 ° C., and further 230 ° C. The film was heat fixed at 200 ° C., relaxed 2% in the transverse direction at 200 ° C., then uniformly cooled and cooled to room temperature to obtain a 50 μm-thick biaxially stretched film. The properties of the obtained film are shown in Table 1. Although the film of this comparative example was excellent in the flame retardance in a film, the flame retardance in the state of a flat cable was not enough. Moreover, hydrolysis resistance and reflectance were also reduced as compared to the examples.

  In Tables 1 and 2, PET represents polyethylene terephthalate, and PEN represents polyethylene-2,6-naphthalenedicarboxylate.

  The flame-retardant biaxially oriented polyester film of the present invention has high flame retardancy without reducing the hydrolysis resistance of polyester such as polyalkylene terephthalate or polyalkylene naphthalate, such as a flexible printed circuit board, It can be suitably used for a flat cable, a solar battery back sheet or a reflector.

Claims (8)

In the flame retardant biaxially oriented polyester film comprising a flame燃基material layer, flame燃基material layer is polyethylene terephthalate or polyethylene naphthalate of 98 wt% or less than 94 wt% based on the weight of the layer, and The phosphinic acid salt represented by the following formula (1) or the diphosphinic acid salt represented by the formula (2) is contained in an amount of 2 wt% or more and less than 6 wt%, and the average particle diameter of the phosphinic acid salt or the diphosphinic acid salt Is 1 μm or more and 5 μm or less, and the average reflectance of the polyester film at a wavelength of 400 to 700 nm is 70% or more and less than 75%,

(Wherein R ¹ and R ² are hydrogen, an alkyl group having 1 to 6 carbon atoms and / or an aryl group, M is a metal, and m is a valence of M)

Wherein R ³ and R ⁴ are hydrogen, an alkyl group having 1 to 6 carbon atoms and / or an aryl group, R ⁵ is an alkylene group having 1 to 6 carbon atoms, an arylene group having 6 to 10 carbon atoms, and an alkylarylene group. Or an arylalkylene group, M represents a metal, and n represents a valence of M.)
A flame retardant biaxially oriented polyester film laminate in which the flame retardant biaxially oriented polyester film and a metal layer are laminated . The flame retardant biaxially oriented polyester film laminate according to claim 1, wherein the flame retardant substrate layer has a thickness of 2 μm or more and 200 μm or less. 2. The flame-retardant biaxially oriented polyester film laminate according to claim 1, wherein the polyester film tensile strength retention after treatment for 10 hours in saturated steam at 121 ° C. and 2 atm is 50% or more. The flame-retardant biaxially oriented polyester film laminate according to claim 1, wherein the film density is 0.7 g / cm ³ or more and 1.3 g / cm ³ or less. 2. The flame-retardant biaxially oriented polyester film laminate according to claim 1, wherein the flame-retardant substrate layer has a surface roughness Ra of 0.1 μm to 2 μm. Used as a flexible printed circuit or flat cable, flame retardant biaxially oriented polyester film laminate according to claim 1. The flame-retardant biaxially oriented polyester film laminate according to claim 1, wherein the flame-retardant base material layer has a heat seal layer on at least one side. The flame-retardant flat cable using the flame-retardant biaxially-oriented polyester film laminated body in any one of Claims 1-7.