JP6061239B2 - Flame retardant imparting agent, flame retardant article and method for producing them - Google Patents

Description

  The present invention relates to a flame retardant imparting agent, a flame retardant article, and a production method thereof.

  With the miniaturization and high performance of electronic devices and communication devices, the importance of heat dissipation has been emphasized, and the development of resin members with high heat dissipation effects has been underway. On the other hand, resin members that are excellent in moldability and have a high degree of design freedom are also used in the field of automobiles. Due to miniaturization and performance improvement of automobile products, measures against heat generation, which has not been emphasized so far, are reviewed, and the demand for higher thermal conductivity is increasing.

  In order to increase the heat dissipation effect of the resin, it is common to increase the thermal conductivity by adding inorganic powders such as oxides as fillers, but in order to achieve further higher thermal conductivity and incombustibility, oxidation is required. Attempts have been made to use nitride powder fillers that have higher thermal conductivity than those of the materials and are expected to improve the heat dissipation effect.

  On the other hand, Patent Document 1 discloses that hexagonal boron nitride dispersed in a polyimide resin is surface-coated with organosilane to improve wettability, increase adhesion with the polyimide resin, flame retardancy and heat A technique for providing a resin material having excellent conductivity is disclosed.

  Patent Document 2 discloses a technique in which a fluorine-modified silicone surfactant is added as a release agent for internal addition in a thermally conductive silicone rubber composition filled with a large amount of boron nitride powder and molded into a sheet shape. Has been.

Japanese Patent Laid-Open No. 9-276992 JP-A-10-204295

  However, nitride powder fillers are generally difficult to uniformly disperse in resin, and even with the techniques described in Patent Document 1 and Patent Document 2, dispersibility is still insufficient in organic polymer materials, It has not reached sufficient flame retardancy. In addition, since it does not have a network structure composed of, for example, Si—O, the organic low molecular weight compound cannot be included in the network structure, and the flame retardancy of the organic low molecular weight compound cannot be improved. Further, in the technique described in Patent Document 1, when added to an organic polymer material, surface characteristics (such as lubricity) obtained by a fluorine-derived compound cannot be imparted.

  The present invention has been made in view of the above-described circumstances, and an object thereof is to provide a flame retardancy imparting agent that imparts high flame retardancy to an organic polymer material.

The flame retardancy imparting agent according to the first aspect of the present invention is characterized by comprising a gelled product having a fluorine-containing oligomer represented by the following general formula (1) as a structural unit and hexagonal boron nitride. To do.
(In the above formula (1), Rf represents a group containing a fluoroalkyl group. N is a natural number.)

In the flame retardancy imparting agent according to the second aspect of the present invention, the hexagonal boron nitride powder is covered with a gelled product having a fluorine-containing oligomer represented by the following general formula (1) as a structural unit, and the average The particle diameter is 10 to 5000 nm.
(In the above formula (1), Rf represents a group containing a fluoroalkyl group. N is a natural number.)

  The ratio of the fluorine-containing oligomer to 100 parts by mass of the hexagonal boron nitride powder is preferably 10 to 400 parts by mass.

The hexagonal boron nitride has a functional group of —OH group and —NH ₂ group on the surface of boron nitride fine particles and is covalently bonded to a boron atom on the end face of the boron nitride crystal. preferable.

The flame retardant article according to the third aspect of the present invention is characterized in that the flame retardant imparting agent according to the first and second aspects is dispersed in an organic material.
The organic material is preferably resin or rubber.

According to a fourth aspect of the present invention, there is provided a method for producing a flame retardant imparting solution comprising a solated solution containing a fluorine-containing oligomer represented by the following general formula (2) and a hexagonal boron nitride powder. Getting and
[Rf− (VM) n−Rf] (2)
(In the above formula (2), Rf represents a group containing a fluoroalkyl group, VM represents CH ₂ —CH—Si (OCH ₃ ) _3, and n is a natural number.)
Obtaining a gelled solution by making the solated solution alkaline,
Removing the solvent from the gelled solution;
It is characterized by providing.

The method for producing a flame retardant article according to the fifth aspect of the present invention is characterized in that the flame retardant imparting agent according to the first and second aspects is dispersed in an organic material.
The organic material is preferably resin or rubber.

  The flame-retardant article according to the sixth aspect of the present invention is characterized in that an organic compound is included in the flame-retardant imparting agent according to the first and second aspects.

  The method for producing a flame retardant article according to the seventh aspect of the present invention is characterized in that the flame retardant imparting agent according to the first and second aspects includes an organic compound.

  According to the flame retardant imparting agent of the present invention, the dispersibility of nitrides in organic materials can be enhanced, and high flame retardancy can be imparted to organic materials such as resins and rubbers.

It is a chart which shows the result of TGA about Examples 1-6. It is a FE-SEM photograph of the composite material which concerns on a comparative example. It is a FE-SEM photograph of the composite material which concerns on an Example. (A)-(f) is a photograph of the PMMA film modified by addition of the composite material of Examples 1-6. 10 is a chart showing the results of UV-vis spectrum for Example 7. It is a chart which shows the result of TGA about Example 7, 8. FIG. 1 is a structural diagram of a composite material (nanocomposite) according to an embodiment of the present invention.

  The present inventors have a functional group on the surface, but since the number of functional groups is small, boron nitride powder having a low affinity with an organic solvent or resin as a simple substance, and a fluorine-containing oligomer having a specific substituent By using a composite material consisting of the above, the above-mentioned problems were solved and a compound having excellent flame retardancy was developed.

  In the following description, the term “flame retardant article” means, for example, an article that does not ignite even if an open flame is brought close to the article in an atmosphere at normal temperature and pressure, or an article that self-extinguishes before being burned even if ignited once , Can be defined as Such articles can also be defined, for example, by the oxygen index. Moreover, in the following description, "providing flame retardancy" is not limited to obtaining such a flame retardant article. For example, it includes not only the case where the oxygen index is set to a certain value or more, but also that the oxygen index is simply set higher than that before imparting flame retardancy.

  Further, in the following description, “boron nitride powder” is referred to as boron nitride powder, and the diameter of the particles constituting the powder is about 10 to 5000 nm. The “particle diameter” is the diameter of fine particles obtained by image analysis of SEM photographs, and the “average particle diameter” is an arithmetic average value (n = 40) of particle diameters.

  Hereinafter, the flame retardancy imparting agent, the flame retardant article, and the production method thereof according to the embodiment of the present invention will be described.

(Flame retarding agent)
The flame retardancy imparting agent according to the embodiment of the present invention includes a gelled product having a fluorine-containing oligomer represented by the following general formula (1) as a constituent unit, and a hexagonal boron nitride (hereinafter referred to as “h-BN”). Is sometimes abbreviated as “.”).
[Fluorine-containing oligomer]

In the above general formula (1), Rf is a group at both ends of the molecule and is a group containing a fluoroalkyl group, specifically, a group represented by —CF (CF ₃ ) OC ₃ F _7. Is preferred.

The compound represented by the above general formula (1) can be obtained by subjecting the fluorine-containing oligomer of the general formula (2) to a sol-gel reaction under acidic or alkaline conditions. In other words, the gelled product having the fluorine-containing oligomer represented by the general formula (1) as a structural unit represents that a network structure (matrix) composed of SiO exists in the intermediate chain.

  The gelled product having the fluorine-containing oligomer represented by the general formula (1) as a structural unit has a molecular weight of 500 in the state of the oligomer before gelation (see the general formula (2) described later). What is about -1000 can be used. Moreover, n is a natural number of 2-3, for example.

  The fluorine-containing oligomer is gelled and has a network structure in the state of the composite material. Since this fluorine-containing oligomer has a large proportion of fluorine atoms (atoms contributing to the improvement of surface characteristics) in one molecule, the fluorine atoms are efficiently applied to the surface of the finally obtained resin molded product or rubber molded product. Can exist. Thereby, the surface characteristics (such as lubricity) of the organic polymer molded product, that is, the resin molded product or the rubber molded product are improved.

[Hexagonal boron nitride powder]
Hexagonal boron nitride powder has functional groups such as —OH groups and —NH ₂ groups on the surface of fine particles made of boron nitride, and is chemically bonded to boron atoms on the end face of the boron nitride crystal by covalent bonds. It is preferable to use one. Here, the end face of the boron nitride crystal refers to a side face perpendicular to the laminated face having a hexagonal network structure in which boron atoms and nitrogen atoms are alternately bonded.

[Composite material (nanocomposite)]
The composite material according to the embodiment of the present invention is in the form of particles, and each particle has a spherical shape or a shape close to a spherical shape (see FIG. 7). Specifically, the composite material is a particulate compound in which a hexagonal boron nitride powder is covered with a gelled product having the fluorine-containing oligomer represented by the general formula (1) as a constituent unit. The average particle diameter is 10 to 5000 nm, preferably 20 to 1000 nm, and more preferably 20 to 500 nm. If the thickness is less than 10 nm, the primary particles aggregate and the handling becomes difficult. On the other hand, if it exceeds 5000 nm, the mechanical properties of the resulting organic polymer molded product may be deteriorated. Thus, because the size of individual particles is nanoscale, this composite material is also called “nanocomposite”.

[Production method of composite material]
The composite material according to the embodiment of the present invention can be produced by reacting the fluorine-containing oligomer represented by the following general formula (2) with the hexagonal boron nitride powder described below by a predetermined method.

  For example, obtaining a solated state solution comprising a fluorine-containing oligomer represented by the following general formula (2) and the above hexagonal boron nitride powder, and making the solated state solution alkaline To obtain a gelled solution and to remove the solvent from the gelled solution.

[Fluorine-containing oligomer]
[Rf− (VM) n−Rf] (2)
(In the above formula (2), Rf is a substituent at both ends of the molecule and represents a group containing a fluoroalkyl group, specifically a group represented by -CF (CF ₃ ) OC ₃ F ₇ ; VM is vinyltrimethoxysilane _{(formula:. CH 2 = CH-Si} (OCH 3) represented by ₃₎ derived from the monomer units (chemical _formula represented by _{CH 2 -CH-Si (OCH 3} ) 3 . represents a) .n is a natural number of 2-3.)

  The ratio of the fluorine-containing oligomer to 100 parts by mass of the hexagonal boron nitride powder is preferably 10 to 400 parts by mass, for example. When the amount exceeds 400 parts by mass, the dispersibility of the hexagonal boron nitride powder in the organic polymer material is saturated, and the manufacturing cost may increase due to the material cost. When the amount is less than 10 parts by weight, the hexagonal nitriding This is because the dispersibility of the boron powder is lowered, and sufficient surface characteristics (such as lubricity) may not be obtained for the organic polymer material.

A reaction formula for obtaining the composite material from the fluorine-containing oligomer and hexagonal boron nitride is represented by the following formula (3).
... Formula (3)

<First Embodiment>
In the first embodiment, a case will be described in which the flame retardant imparting agent (composite material) is added to an organic polymer compound (base material) as described below. Thereby, the thermal conductivity of the organic polymer compound can be improved, and as a result, high flame retardancy can be imparted to the obtained flame-retardant article.

(Organic polymer compound)
As the organic polymer material imparting flame retardancy, for example, resin and rubber can be used.

  Examples of the resin include polyimide resin, polymethyl methacrylate (PMMA), nylon 6 (Tm = 215 ° C.), nylon 66 (Tm = 255 ° C.), polyimide, polyphenylene oxide, noryl, polysulfone, TPX (registered by Mitsui Chemicals, Inc.) (Trademark; a kind of polymethylpentene), a thermoplastic resin having flame retardancy such as polyacetal, polycarbonate and the like, but is not limited thereto. Among these, a polyimide resin is preferably used because it is excellent not only in flame retardancy but also in cold resistance, mechanical properties, and electrical properties.

  As rubber, for example, chloroprene rubber (CR), fluorine rubber (FKM, FEPM), chlorosulfonated polyethylene (CSM), chlorinated polyethylene, epichlorohydrin rubber and other flame retardant rubber (elastomer), nitrile rubber Mention may also be made of rubbers (elastomers) which are not usually flame retardant, such as (NBR), butyl rubber (IIR), ethylene propylene rubber (EPM, EPDM), silicone and the like.

  In addition, examples of the organic polymer material that can impart flame retardancy include paper, wood, and fabric. In the case of these substances, as described later, they are used by being applied to the surface thereof. .

[Method for producing flame-retardant article]
These organic polymer materials are generally heated and melted, mixed with a flame retardant imparting agent, and then molded into a predetermined shape with a mold to form a flame retardant article.

  The content of the composite material with respect to the organic polymer material is 0.01 to 1000 parts by mass, preferably 0.5 to 100 parts by mass, more preferably 1 to 100 parts by mass with respect to 100 parts by mass of the organic polymer material. It is good to do. If it is less than 0.01 parts by mass, the heat conductivity, flame retardancy, lubricity, chemical stability, corrosion resistance, and surface properties of the obtained molded product cannot be sufficiently improved, and if it exceeds 1000 parts by mass This is because mechanical properties such as flexibility and elasticity of the obtained resin molded product may be deteriorated.

  For example, when the organic polymer material is a polyimide resin, the composite material is 0.01 to 1000 parts by weight, preferably 0.5 to 100 parts by weight, more preferably 1 to 100 parts by weight of the polyimide resin. It is good to set it as 100 mass parts.

  When the organic polymer material is chloroprene rubber, the composite material is 0.01 to 1000 parts by weight, preferably 0.5 to 100 parts by weight, and more preferably 1 to 100 parts by weight with respect to 100 parts by weight of chloroprene rubber. It is good to set it as 100 mass parts.

In this embodiment, the mechanism by which flame retardancy is exhibited by adding a composite material to an organic polymer material can be estimated as follows.
That is, as shown in FIG. 7, when the above fluorine-containing oligomer is used, a sol-gel reaction occurs under an alkaline condition to form a core-shell (BN-VM-surface having Rf group) structure. . For this reason, when a composite material having an organic polymer material is baked at 800 ° C., the hydrocarbon group of the RF group and the VM burns. However, the Si—O matrix and BN remain in the organic polymer material, and it is considered that the flame retardancy of the polymer material is enhanced particularly by the thermal conductivity of BN.

  In addition, according to the present embodiment, since the fluorine-containing oligomer contains an Rf group, that is, fluorine, surface characteristics (such as lubricity) that can be obtained by a fluorine-derived compound can be imparted.

Second Embodiment
The composite material according to the embodiment of the present invention, as in the second embodiment, is added to the organic polymer compound as in the first embodiment to enhance the flame retardancy. It is also possible to increase the flame retardancy of the resulting flame retardant article by incorporating an organic low molecular weight compound.

(Organic low molecular weight compound)
Examples of organic low molecular weight compounds that increase flame retardancy include bisphenol AF (BPAF) (2,2-bis (4-hydroxyphenyl) hexafluoropropane), bisphenol A (2,2-bis (4-hydroxyphenyl) propane) Bisphenol F (bis (4-hydroxyphenyl) methane), binol A ((2R, 7Z) -3-methylene-7,11,11-trimethylbicyclo [8.1.0] undec-7-ene-2β, Organic compounds such as 6α-diol).

[Method for producing flame-retardant article]
In this embodiment, a flame retardant article is obtained by including a low molecular weight organic compound in a composite material.

  In this case, it is preferable that the addition amount of the organic low molecular weight compound with respect to 100 parts by mass of the composite material is 50 parts by mass or less. This is because if it exceeds 50 parts by mass, it may be difficult to encapsulate (encapsulate) the organic low-molecular compound in the network structure.

(Encapsulation reaction formula)
In the present embodiment, for example, a fluorine-containing oligomer is obtained from a fluorine-containing oligomer / hexagonal boron nitride (h-BN) composite material and BPAF, which is an organic low-molecular compound, by the reaction formula shown by the following formula (4). / Hexagonal boron nitride / BPAF composite material can be obtained.

... Formula (4)

  In the present embodiment, the reason why flame retardancy is enhanced by including BPAF, which is a low molecular weight organic compound, in the fluorine-containing oligomer / hexagonal boron nitride composite material is that BPAF is a network of gelled products of fluorine-containing oligomers. This is presumably because they are encapsulated in the structure (Si—O bond).

  According to this embodiment, the characteristics inherent to the low molecular weight organic compound, such as fluorescence characteristics, can be used even at high temperatures or in a flammable environment.

[Example]
Hereinafter, the present invention will be described more specifically with reference to examples. However, the flame retardancy imparting agent (the composite material) and the production method thereof according to the present invention are not limited to the following examples. Note that the unit% represents mass% unless otherwise specified.

<Examples 1-6>
Examples 1 to 6 correspond to the first embodiment, and are examples of cases where a composite material is added to an organic polymer material to improve the flame retardancy and surface characteristics of the organic polymer material. is there.

  First, in accordance with the formulation shown in Table 1 below, a fluorine-containing oligomer and a hexagonal boron nitride filler were added to a 50 ml sample bottle containing 12 ml of methanol at room temperature (25 ° C.) in the amounts shown in Table 1 below. (Average particle diameter: about 70 nm), manufactured by MARUKA Co., Ltd.) was added, and the mixture was stirred for several minutes to several hours. Furthermore, at room temperature (25 ° C.), 5 ml of 25% aqueous ammonia was added and reacted for 5 hours. Here, the completion of the reaction can be confirmed by cloudiness or sedimentation of the precipitate.

  After completion of the reaction, the solvent was removed from the solution using an evaporator (80 to 100 ° C.), and the solvent was completely removed by vacuum drying (50 ° C.) for 1 day.

  Thereafter, the reaction product after removal of the solvent is again stirred and dispersed in methanol for several hours, and further, a fluorine-containing oligomer / hexagonal boron nitride nanocomposite (hereinafter referred to as “composite material”) is used using a centrifugal separator. Obtained as a precipitate. The above results are summarized in Table 1 below.

Note) Yield (%) is based on the raw material fluorine-containing oligomer / hexagonal boron nitride.
The measurement was performed by a dynamic light scattering method (DLS: Dynamic Light Scattering Measurement) (manufactured by Otsuka Electronics Co., Ltd., model number: DLS-7000HL).
Rf: molecular chain terminal group represented by —CF (CF ₃ ) OC ₃ F ₇ VM: molecular chain intermediate group represented by CH ₂ —CH—Si (OCH ₃ ) ₃ h-BN: hexagonal boron nitride Powder was also fired in an air atmosphere at a temperature rising rate of 10 ° C./min and a temperature rising from room temperature to 800 ° C. (the same applies in the following description).

[Thermal stability of composite materials]
Regarding the thermal stability of the fluorine-containing oligomer / hexagonal boron nitride composite material obtained in Examples 1 to 6, using a high-temperature differential scanning calorimeter (TGA) in an air atmosphere at a heating rate of 10 ° C./min. Measured from room temperature to 800 ° C. As the high-temperature differential scanning calorimeter, model number: TG-DTA2000SA manufactured by Bruker AXS Co., Ltd. was used. The obtained results are shown in FIG.

From the result of TGA shown in FIG. 1, it can be confirmed that the degree of weight decrease when the temperature exceeds 300 ° C. increases as the ratio of the fluorine-containing oligomer to the hexagonal boron nitride increases. The percentage reduction in mass at 800 ° C. with respect to room temperature is as follows: hexagonal boron nitride (h-BN) alone: 1%, Example 1: 7%, Example 2: 10%, Example 3: 20%, example 4: 30%, example 5: 43%, example 6 54%, a fluorine-containing oligomer over single body represented by the general formula (1) was 62%. This change shows that there is almost no decrease in weight due to heating of hexagonal boron nitride (about 1 to 2%), and the weight reduction rate due to heating of the fluorine-containing oligomer at 500 ° C. or higher is high (about 60%). Therefore, it can be said that it originates from a fluorine-containing oligomer.

  About the composite material obtained in Examples 1-6, it adds to an organic polymer material by the method shown in the following (1) and (2), and also after the composite material addition by the method shown below. Dispersibility, surface characteristics, and flame retardancy of organic polymer materials were evaluated. In addition, although it can also add to an organic polymer material like (3), the content of experiment is not shown about this content.

  (1) A composite material is added to an organic polymer material in a molten state and stirred to disperse the composite material. Thereafter, the composite material is injected or cast into a mold cavity, cooled, and molded.

  (2) A composite material is added and dispersed in a solution in which an organic polymer material is dissolved in a solvent, and then the solvent is removed to form. Specifically, a polymer solution in which a composite material is added and dispersed is poured into a petri dish, and then the solvent is removed to prepare a polymer film.

  (3) A composite material dispersion solution is applied to a base material (metal, glass, rubber, resin, fabric, wood, paper, etc.) by spraying, dipping, or the like to form a film on the surface of the base material. Here, it may be a degree to modify the surface of the substrate.

[Dispersibility]
The dispersibility of the composite materials obtained in Examples 1 to 6 was evaluated as follows.

  That is, a solution prepared by dispersing a hexagonal boron nitride filler in methanol (comparative example) and a solution prepared by dispersing a fluorine-containing oligomer / hexagonal boron nitride composite material (here, Example 4) in methanol. Were evaluated using an FE-SEM (Field Emission scanning electron microscope) (manufactured by JEOL Ltd., model number: JSM-7000F).

  As shown in FIG. 2 (Comparative Example), particles are aggregated in a single hexagonal boron nitride filler. On the other hand, by making hexagonal boron nitride and fluorine-containing oligomer into a composite material by the above-described method, the composite material is separated into particles as shown in FIG. (See the left-side photo in FIG. 3). By the way, although an FE-SEM photograph is not shown, hexagonal boron nitride has a —OH group and is well (single) dispersed well in water. On the other hand, when the hexagonal boron nitride and the fluorine-containing oligomer are made into a composite material by the above-described method, they are not dispersed in water. That is, water repellency is increased. In addition, there was no change in the particle form of the composite material after firing (see the right-hand photo in FIG. 3).

[Surface characteristics]
From the composite materials obtained in Examples 1 to 6, the surface characteristics of the organic polymer material prepared and mixed and dispersed by the method (2) were evaluated as follows.

  That is, first, dodecane (hereinafter referred to as oil) is formed on a polymethyl methacrylate (PMMA) film obtained by dispersing, mixing, and modifying a fluorine-containing oligomer / hexagonal boron nitride composite material prepared in Examples 1 to 6. ) And water are dropped, and the angle (unit: ° (degree)) formed at the contact portion between the film, the oil droplet, and the water droplet is measured by a contact angle measuring device (manufactured by Kyowa Interface Science Co., Ltd., model number: DropMaster-301 (DM -301)). The higher the value of the contact angle, the easier it is to repel oil and water, that is, higher antifouling properties and water repellency.

  As shown in Table 2 below, from the contact angle of the subject (PMMA film) corresponding to Examples 1 to 6, high oil repellency and water repellency are exhibited on the front side of the PMMA film. Indicated. Furthermore, when the VM addition amount was 50 to 400 mg, the oil contact angle was 0 (zero) on the back surface (reverse side, contact surface with the petri dish) of the PMMA film.

  From the results shown in Table 2 above, when the amount of fluorine-containing oligomer added is large (for example, 50 to 400 mg; Examples 3 to 6), the contact angle on the back surface is 0 ° and oil repellency is exhibited in the case of oil. It can be estimated that the fluorinated alkylene group (Rf) is oriented on the front surface of the PMMA film. In other words, in Examples 3 to 6, in the solution state, the composite material is uniformly dispersed in the solvent (see FIG. 3), but when the PMMA film modified by the above-described method is formed, the composite material is used. It can be presumed that the composite material moves to the vicinity of the film surface in the process of removing the solvent from the dispersed solution in the petri dish.

  On the other hand, when the addition amount of the fluorine-containing oligomer is small (for example, 10 to 20 mg; Examples 1 and 2), the surface orientation of fluorine becomes low, so that oil repellency is also exhibited on the reverse side of the film. To come. In other words, in Examples 1 and 2 in which the amount of fluorine-containing oligomer added is small, it can be estimated that in the film state, the composite material is uniformly dispersed in the thickness direction of the film in addition to the plane direction of the film. . As described above, by making the hexagonal boron nitride and the fluorine-containing oligomer into a composite material by the above-described method, depending on the blending amount of the fluorine-containing oligomer, the action of the fluorinated alkylene group (Rf) causes water repellency / Oil repellency can be expressed.

(Dispersibility of hexagonal boron nitride)
4 (a) to 4 (f) show photographs of PMMA films modified by adding the composite materials of Examples 1 to 6, respectively. As described above, in the method (2), the composite materials of Examples 1 to 6 did not aggregate hexagonal boron nitride, and were able to produce a uniform and highly transparent PMMA film. Thus, in the fluorine-containing oligomer / hexagonal boron nitride composite material in each of Examples 1 to 6, it was confirmed that the hexagonal boron nitride showed high dispersibility.

<Examples 7 and 8>
Examples 7 and 8 correspond to the second embodiment, and are experimental examples in which a low-molecular organic compound is included in a composite material to obtain a flame-retardant article. In Examples 7 and 8, flame retardant articles were prepared as follows, and the flame retardancy was evaluated.

  First, in accordance with the formulation shown in Table 3 below, a fluorine-containing oligomer, a hexagonal boron nitride filler (average particle size: about 70 nm, manufactured by MARUKA Corporation), bisphenol AF (BPAF) were placed in a 50 ml sample bottle containing 12 ml of methanol. ) And stirred at room temperature (25 ° C.) for several minutes to several hours.

  Subsequently, 5 ml of 25% aqueous ammonia was added at room temperature (25 ° C.) and reacted for 5 hours. After completion of the reaction, the solvent was removed by an evaporator (80 to 100 ° C.), followed by vacuum drying (50 ° C.) for 1 day to completely remove the solvent.

  Thereafter, the reaction product after removal of the solvent is again stirred and dispersed in methanol for several hours, and the target fluorine-containing oligomer / hexagonal boron nitride / BPAF nanocomposite (hereinafter referred to as “composite material”) is used. Was obtained as a precipitate. The above results are summarized in Table 3 below.

Note) Yield (%) is based on the raw material fluorine-containing oligomer / hexagonal boron nitride.
The measurement was performed by a dynamic light scattering method (DLS: Dynamic Light Scattering Measurement).

  About the product obtained in Example 7, the UV-vis spectrum was measured with the UV-vis apparatus (Shimadzu Corporation make, model number UV-1800). The obtained spectrum result is shown in FIG.

  From the results of the UV-vis spectrum shown in FIG. 5, it can be seen that BPAF is included in the fluorine-containing oligomer / hexagonal boron nitride composite material.

[Thermal stability]
Regarding the thermal stability (flame retardancy) of the fluorine-containing oligomer / hexagonal boron nitride / BPAF composite material obtained in Examples 4, 7, and 8, using a high-temperature differential scanning calorimeter (TGA) in an air atmosphere The temperature was measured from room temperature to 800 ° C. at a heating rate of 10 ° C./min. The obtained TGA results are shown in FIG. Here, the percentage reduction in mass at 800 ° C. with respect to room temperature is as follows: hexagonal boron nitride (h-BN) alone: 1%, Example 4: 30%, Example 7: 31%, Example 8: 31%, the fluorine-containing oligomer over single body represented by the general formula (1) was 62%.

  FIG. 6 shows that the fluorine-containing oligomer / hexagonal boron nitride / BPAF composite material has the same heat as the fluorine-containing oligomer / hexagonal boron nitride composite material even though BPAF is included in the composite material. Draw a weight loss curve. From this result, it can be estimated that the encapsulated BPAF is not combusted at 800 ° C. Therefore, it can be said that incombustibility of the low molecular weight organic compound has been realized.

Claims (11)

A flame retardancy imparting agent comprising a gelled product having a fluorine-containing oligomer represented by the following general formula (1) as a structural unit and hexagonal boron nitride.
(In the above formula (1), Rf represents a group containing a fluoroalkyl group. N is a natural number.) Flame retardancy characterized in that hexagonal boron nitride powder is covered with a gelled product containing a fluorine-containing oligomer represented by the following general formula (1) as a structural unit, and the average particle size is 10 to 5000 nm. Giving agent.
(In the above formula (1), Rf represents a group containing a fluoroalkyl group. N is a natural number.)   The flame retardancy imparting agent according to claim 1 or 2, wherein a ratio of the fluorine-containing oligomer to 100 parts by mass of the hexagonal boron nitride powder is 10 to 400 parts by mass. The hexagonal boron nitride has a functional group of —OH group and —NH ₂ group on the surface of the boron nitride fine particles and is covalently bonded to a boron atom on the end face of the boron nitride crystal. The flame retardancy imparting agent according to any one of claims 1 to 3, wherein   A flame retardant article, wherein the flame retardant imparting agent according to any one of claims 1 to 4 is dispersed in an organic material.   The flame retardant article according to claim 5, wherein the organic material is resin or rubber. Obtaining a solated solution comprising a fluorine-containing oligomer represented by the following general formula (2) and a hexagonal boron nitride powder;
[Rf− (VM) n−Rf] (2)
(In the above formula (2), Rf represents a group containing a fluoroalkyl group, VM represents CH ₂ —CH—Si (OCH ₃ ) _3, and n is a natural number.)
Obtaining a gelled solution by making the solated solution alkaline,
Removing the solvent from the gelled solution;
A method for producing a flame retardant imparting agent, comprising:   A method for producing a flame retardant article, comprising dispersing the flame retardant imparting agent according to any one of claims 1 to 4 in an organic material.   The method for producing a flame-retardant article according to claim 8, wherein the organic material is resin or rubber.   5. A flame retardant article, wherein an organic compound is included in the flame retardant agent according to any one of claims 1 to 4.   A method for producing a flame-retardant article, wherein the flame retardant imparting agent according to any one of claims 1 to 4 is incorporated with an organic compound.