Patent Application
20230407076
The present invention relates to a polymer comprising a specific phosphorus-containing structural unit, a flame-retardant composition comprising the polymer, and a method for producing the polymer.
A resin comprising methyl methacrylate (MMA) as a main component is excellent in characteristics such as high transparency and weather resistance, and is used for various applications. In recent years, the application of the resin to building materials and the like utilizing transparency and design property has been promoted, but high flame retardancy is required in these applications.
As a method of imparting flame retardancy, for example, methods as described in PTLs 1 and 2 have been studied. Specifically, PTL 1 discloses a methacrylic resin composition obtained by polymerizing a polymerizable composition comprising a monomer composition, a phosphoric acid ester, and an antioxidant, and describes a halogenated phosphoric acid ester and the like as the phosphoric acid ester. Moreover PTL 2 discloses a flame-retardant acrylic artificial marble obtained by curing a composition comprising a resin component, an inorganic filler, a crosslinkable vinyl monomer, and an acrylic acid ester and/or a crosslinkable vinyl monomer, and describes aluminum hydroxide and the like as the inorganic filler.
In PTL 1, a halogen-containing compound is used, but there are problems that dehalogenation is desired from the viewpoint of environmental load and the like, and that a toxic gas is generated at the time of combustion. Further, when an inorganic flame retardant is added as in PTL 2, there is a problem that turbidity is generated and transparency is lost. Furthermore, when a large amount of flame retardant is added in order to improve flame retardancy, the performance of the cast plate itself is deteriorated, and further, since a resin softens during combustion, there is a problem of inducing ignition to the surroundings.
Therefore, an object of the present invention is to provide a polymer which is excellent in flame retardancy and is less likely to cause deterioration in physical properties such as softening at the time of heating; and a flame-retardant composition, and a method for producing the polymer.
As a result of intensive studies in order to solve the above-described problems, the present inventors have found that when a polymer comprises a specific phosphorus-containing structural unit, the polymer has excellent flame retardancy and is less likely to cause a decrease in physical properties such as softening at the time of heating, and have thus completed the present invention.
That is, the present invention provides the following [1] to [12].
[1] A polymer comprising a structural unit represented by the following general formula (I).
In the general formula (I), R1 represents a hydrogen atom or a methyl group; R2 and R3 each independently represent any one selected from the group consisting of an alkyl group having 1 to 6 carbon atoms, an alkyloxy group having 1 to 6 carbon atoms, an alkenyl group having 2 to 6 carbon atoms, an alkenyloxy group having 2 to 6 carbon atoms, an aralkyl group having 7 to 12 carbon atoms, an aralkyloxy group having 7 to 12 carbon atoms, an aryl group having 6 to 12 carbon atoms, and an aryloxy group having 6 to 12 carbon atoms, and R2 and R3 may be bonded to each other; and n is an integer of 0 to 7.
[2] The polymer as set forth in [1], wherein n in the general formula (I) is 5.
[3] A flame-retardant composition comprising the polymer as set forth in [1] or [2].
[4] A flame-retardant sheet or flame-retardant plate obtained by using the polymer as set forth in [1] or [2] or the flame-retardant composition as set forth in [3].
[5] A compound (A) represented by the following general formula (II).
In the general formula (II), R11 represents a hydrogen atom or a methyl group; R12 and R13 each independently represent any one selected from the group consisting of an alkyl group having 1 to 6 carbon atoms, an alkyloxy group having 1 to 6 carbon atoms, an alkenyl group having 2 to 6 carbon atoms, an alkenyloxy group having 2 to 6 carbon atoms, an aralkyl group having 7 to 12 carbon atoms, an aralkyloxy group having 7 to 12 carbon atoms, an aryl group having 6 to 12 carbon atoms, and an aryloxy group having 6 to 12 carbon atoms, and R12 and R13 may be bonded to each other; and m is an integer of 0 to 7.
[6] The compound (A) as set forth in [5], wherein m in the general formula (II) is 5.
[7] A method for producing a polymer, comprising a step of polymerizing a compound (B) represented by the following general formula (III) and a polymerizable monomer (C) in the presence of at least one phosphorous acid-based ester compound (D) selected from the group consisting of a phosphinous acid ester compound, a phosphonous acid monoester compound, and a phosphorous acid diester compound.
In the general formula (III), R21 represents a hydrogen atom or a methyl group, and p is an integer of 0 to 7.
[8] The method for producing a polymer as set forth in [7], wherein the compound (B) is represented by the following general formula (IV).
In the general formula (IV), R31 represents a hydrogen atom or a methyl group.
[9] The method for producing a polymer as set forth in [7] or [8], wherein an addition amount of the phosphorous acid-based ester compound (D) is 40 to 160 mol % with respect to 100 mol % of the compound (B).
A composition comprising a compound (B) represented by the following general formula (III), a polymerizable monomer (C), and at least one phosphorous acid-based ester compound (D) selected from the group consisting of a phosphinous acid ester compound, a phosphonous acid monoester compound, and a phosphorous acid diester compound.
In the general formula (III), R21 represents a hydrogen atom or a methyl group, and p is an integer of 0 to 7.
The composition as set forth in [10], wherein the compound (B) is represented by the following general formula (IV).
In the general formula (IV), R31 represents a hydrogen atom or a methyl group.
The composition as set forth in [9] or [10], wherein a content of the phosphorous acid-based ester compound (D) is 40 to 160 mol % with respect to 100 mol % of the compound (B).
According to the present invention, it is possible to provide a polymer which is excellent in flame retardancy and hardly causes deterioration in physical properties such as softening at the time of heating; and a flame-retardant composition, and a method for producing the polymer.
Hereinafter, an example of an embodiment of the present invention (hereinafter, may be referred to as “the present embodiment”) will be described. However, the embodiments described below are examples for embodying the technical idea of the present invention, and the present invention is not limited to the following description.
In addition, in the description herein, preferred embodiments are shown, but a combination of two or more of individual preferred embodiments is also a preferred embodiment. Regarding the matters indicated by the numerical ranges, in a case where there are several numerical ranges, it is possible to selectively combine the lower limit value and the upper limit value thereof to obtain a preferred embodiment.
Moreover, in the description herein, when there is a description of a numerical range of “XX to YY”, it means “XX or more and YY or less”. Further, in the description herein, “(meth)acrylate” means methacrylate and acrylate.
Since the polymer of the present embodiment comprises a specific phosphorus-containing structural unit, the polymer is excellent in flame retardancy and can suppress deterioration in physical properties such as softening at the time of heating.
The flame-retardant composition comprising the polymer has a low combustion rate and almost no combustion drips. Further, by using the polymer or the flame-retardant composition, it is possible to provide a flame-retardant sheet and a flame-retardant plate having excellent flame retardancy.
In addition, the polymer can be easily obtained by employing a specific step included in the method for producing a polymer. Then, by employing the compound represented by the general formula (II), it is possible to exhibit good performance with respect to flame retardancy.
The polymer of the present embodiment comprises a structural unit represented by the following general formula (I).
The reason why the polymer of the present embodiment improves the flame retardancy is not clear, but it is considered that one of the reasons is that the polymer contains a large amount of phosphorus-carbon bonds consumable of a large amount of oxygen at the time of combustion, and thus the flame retardancy is improved.
In the general formula (I), R1 represents a hydrogen atom or a methyl group, and from the viewpoint of polymerization operability, a methyl group is preferable.
In the general formula (I), R2 and R3 each independently represent any one selected from the group consisting of an alkyl group having 1 to 6 carbon atoms, an alkyloxy group having 1 to 6 carbon atoms, an alkenyl group having 2 to 6 carbon atoms, an alkenyloxy group having 2 to 6 carbon atoms, an aralkyl group having 7 to 12 carbon atoms, an aralkyloxy group having 7 to 12 carbon atoms, an aryl group having 6 to 12 carbon atoms, and an aryloxy group having 6 to 12 carbon atoms. R2 and R3 may be bonded to each other.
In the general formula (I), examples of the alkyl group having 1 to 6 carbon atoms represented by R2 and R3 include a methyl group, an ethyl group, a n-propyl group, an isopropyl group, a n-butyl group, an isobutyl group, a sec-butyl group, a tert-butyl group, a n-pentyl group, an isopentyl group, a neopentyl group, a n-hexyl group, a cyclopropyl group, a cyclobutyl group, a cyclopentyl group, and a cyclohexyl group.
In the general formula (I), examples of the alkyloxy group having 1 to 6 carbon atoms represented by R2 and R3 include a methoxy group, an ethoxy group, a n-propyloxy group, an isopropyloxy group, a n-butyloxy group, an isobutyloxy group, a sec-butyloxy group, a tert-butyloxy group, a n-pentyloxy group, an isopentyloxy group, a neopentyloxy group, a n-hexyloxy group, a cyclopropyloxy group, a cyclobutyloxy group, a cyclopentyloxy group, and a cyclohexyloxy group.
In the general formula (I), examples of the alkenyl group having 2 to 6 carbon atoms represented by R2 and R3 include a vinyl group, an allyl group, a propenyl group, an isopropenyl group, a butenyl group, an isobutenyl group, a pentenyl group, a hexenyl group (such as a cis-3-hexenyl group), and a cyclohexenyl group.
In the general formula (I), examples of the alkenyloxy group having 2 to 6 carbon atoms represented by R2 and R3 include a vinyloxy group, an allyloxy group, a propenyloxy group, an isopropenyloxy group, a butenyloxy group, an isobutenyloxy group, a pentenyloxy group, a hexenyloxy group (such as a cis-3-hexenyloxy group), and a cyclohexenyloxy group.
In the general formula (I), examples of the aralkyl group having 7 to 12 carbon atoms represented by R2 and R3 include a benzyl group, a 2-phenylethyl group, and a 2-phenylpropyl group.
In the general formula (I), examples of the aralkyloxy group having 7 to 12 carbon atoms represented by R2 and R3 include a benzyloxy group, a 2-phenylethyloxy group, and a 2-phenylpropyloxy group.
In the general formula (I), examples of the aryl group having 6 to 12 carbon atoms represented by R2 and R3 include a phenyl group, a 2-methylphenyl group, a 2,4-dimethylphenyl group, and a 2-naphthyl group.
In the general formula (I), examples of the aryloxy group having 6 to 12 carbon atoms represented by R2 and R3 include a phenoxy group, a 2-methylphenoxy group, a 2,4-dimethylphenoxy group, and a 2-naphthoxy group.
Among these, from the viewpoint of improving the flame retardancy, R2 and R3 are preferably an ethoxy group, a n-butyloxy group, a phenoxy group, and a phenyl group, and more preferably a phenoxy group and a phenyl group.
In the general formula (I), examples of the structure of the phosphorus atom-containing portion including R2 and R3 include the following structures.
Among these, from the viewpoint of improving the flame retardancy of the obtained polymer and flame-retardant composition, the structure of the phosphorus atom-containing portion including R2 and R3 preferably has the following structure.
In the general formula (I), n is an arbitrary integer of 0 to 7, and from the viewpoint of improving the physical properties at the time of heating of the obtained polymer and the flame-retardant composition, n is preferably 2 to 6, more preferably 3 to 6, and still more preferably 5.
The content of the structural unit represented by the general formula (I) in the polymer of the present embodiment is preferably 1 to 99% by mass, more preferably 5 to 80% by mass, still more preferably 10 to 70% by mass, and even more preferably 10 to 60% by mass. When the content of the structural unit represented by the general formula (I) is within the above range, deterioration in physical properties such as softening at the time of heating can be further easily suppressed while improving the flame retardancy.
The polymer of the present embodiment can comprise a structural unit other than the structural unit represented by the general formula (I). For example, by including a structural unit derived from the polymerizable monomer (C), the polymer can express a decorative property or the like.
Examples of the polymerizable monomer (C) include vinyl monomers, (meth)acrylic acid alkyl esters, (meth)acrylic acid esters, (meth)acrylates, and unsaturated dicarboxylic acids. As the (meth)acrylic acid ester, for example, those having a cyclic structure, a hydroxy group, or an epoxy group at a terminal can be used. In addition, as the (meth)acrylate, for example, those having an alkylene glycol structure or a silane or silyl group at a terminal can be used.
Examples of the vinyl monomer include styrene, 2-methylstyrene, vinyl acetate, and vinyl chloride.
Examples of the (meth)acrylic acid alkyl ester include methyl(meth)acrylate, propyl(meth)acrylate, butyl(meth)acrylate, pentyl(meth)acrylate, hexyl(meth)acrylate, and 2-ethylhexyl (meth)acrylate.
Examples of the (meth)acrylic acid ester having a cyclic structure include cyclohexyl(meth)acrylate, dicyclopentanyl(meth)acrylate, dicyclopentenyl(meth)acrylate, dicyclopentenyloxyethyl(meth)acrylate, adamantyl(meth)acrylate, 3-hydroxyadamantyl(meth)acrylate, and 2-methyl-2-adamantyl (meth)acrylate.
Examples of the (meth)acrylic acid ester having a hydroxy group include 2-hydroxyethyl(meth)acrylate, hydroxypropyl(meth)acrylate, hydroxybutyl(meth)acrylate, and caprolactone-modified 2-hydroxyethyl (meth)acrylate.
Examples of the (meth)acrylic acid ester having an epoxy group at a terminal include glycidyl (meth)acrylate and (3,4-epoxycyclohexyl)methyl (meth)acrylate.
Examples of the (meth)acrylate having an alkylene glycol structure include methoxydiethylene glycol (meth)acrylate, ethoxydiethylene glycol (meth)acrylate, isooctyloxydiethylene glycol (meth)acrylate, phenoxytriethylene glycol (meth)acrylate, methoxytriethylene glycol (meth)acrylate, and methoxypolyethylene glycol (meth)acrylate.
Examples of the silane- or silyl group-terminated (meth)acrylate include 2-trimethylsiloxyethyl (meth)acrylate.
Examples of the unsaturated dicarboxylic acid include maleic anhydride and derivatives thereof.
Moreover, as the polymerizable monomer (C), a compound having two or more polymerizable groups in the molecule (excluding the compound (B) described later) may be used. Examples of the compound having two or more polymerizable groups in the molecule include ethylene glycol di(meth)acrylate, diethylene glycol di(meth)acrylate, dipropylene glycol di(meth)acrylate, tripropylene glycol di(meth)acrylate, 1,3-butane diol di(meth)acrylate, 1,4-butanediol di(meth)acrylate, 1,6-hexanediol di(meth)acrylate, neopentyl glycol di(meth)acrylate, 1,9-nonanediol di(meth)acrylate, 1,10-decanediol di(meth)acrylate, tricyclodecane dimethanol di(meth)acrylate, glycerol di(meth)acrylate, di(meth)acrylate of hydrogenated bisphenol A or hydrogenated bisphenol F, polyethylene glycol di(meth)acrylate, polypropylene glycol di(meth)acrylate, pentaerythritol tetra(meth)acrylate, dipentaerythritol hexa(meth)acrylate, and trimethylolpropane tri(meth)acrylate.
Further, as the polymerizable monomer (C), a hydroxy group-containing polyfunctional (meth)acrylic acid ester may be used. Examples of the hydroxy group-containing polyfunctional (meth)acrylic acid ester include glycerol di(meth)acrylate, trimethylolpropane di(meth)acrylate, pentaerythritol tri(meth)acrylate, pentaerythritol di(meth)acrylate, and dipentaerythritol monohydroxypenta(meth)acrylate.
Among these polymerizable monomers (C), from the viewpoint of processability and decorative property, methyl (meth)acrylate and butyl (meth)acrylate are preferable and methyl methacrylate is more preferable. These polymerizable monomers (C) may be used alone, or two or more thereof may be used in combination.
The content of the structural unit derived from the polymerizable monomer (C) in the polymer of the present embodiment is not particularly limited, but is preferably 1 to 99% by mass, more preferably 10 to 98% by mass, still more preferably 30 to 95% by mass, and even more preferably 40 to 90% by mass. When the content of the structural unit derived from the polymerizable monomer (C) is within the above range, the processability and the decorative property of the polymer can be improved while improving the flame retardancy.
The polymerizable monomer (C) may be polymerized to some extent before being mixed with other components and then used as a syrup for the purpose of improving the operability and shortening the polymerization time. This operation may be applied to all parts of the polymerizable monomer (C), or may be applied to only a part of the polymerizable monomer (C).
The polymer of the present embodiment can be produced by applying a known polymerization method such as cationic polymerization, anionic polymerization, or radical polymerization to a polymerizable monomer formable of a structural unit represented by the general formula (I).
As a polymerizable monomer formable of the structural unit represented by the general formula (I), a compound (A) represented by the following general formula (II) may be used. For example, a method (1) for producing a polymer, in which a raw material composition comprising the compound (A) and the polymerizable monomer (C) as an optional component is polymerized by the above-described known polymerization method, can be employed.
By using the compound (A), a polymer comprising a structural unit represented by the general formula (I) can be obtained, and a large amount of phosphorus atoms can be contained in the molecular structure of the polymer. Therefore, elution, bleeding (also referred to as bleed out), and the like of a phosphorus-containing component due to heating do not occur, and good performance can be maintained.
In the general formula (II), R11, R12, and R13 are the same as R1, R2, and R3 in the general formula (I), respectively, and redundant description is omitted here.
Preferred embodiments of R11, R12, and R13 are also the same as those of R1, R2, and R3 in the general formula (I), respectively, and redundant description is omitted here.
In the general formula (II), m is an arbitrary integer of 0 to 7, and from the viewpoint of improving the physical properties at the time of heating of the obtained polymer and the flame-retardant composition, m is preferably 2 to 6, more preferably 3 to 6, and still more preferably 5.
The compound (A) can be synthesized, for example, by utilizing and applying known chemical reactions.
In the method (1) for producing a polymer, the addition amount of the compound (A) is not particularly limited, but from the viewpoint of improving the flame retardancy of the flame-retardant composition described later, when the total amount of the raw materials is 100 parts by mass, it is preferably 0.1 parts by mass or more, more preferably 1.0 parts by mass or more, and still more preferably 5.0 parts by mass or more. Whereas, from the viewpoint of moldability, when the total amount of the raw materials is 100 parts by mass, the upper limit of the addition amount of the compound (A) is preferably 50 parts by mass or less, more preferably 30 parts by mass or less, and may be 20 parts by mass or less.
The method for producing a polymer of the present embodiment can be, besides the method (1) for producing a polymer described above, a production method (2) comprising a step of polymerizing a compound (B) represented by the general formula (III) and a polymerizable monomer (C) in the presence of at least one phosphorous acid-based ester compound (D) selected from the group consisting of a phosphinous acid ester compound, a phosphonous acid monoester compound, and a phosphorous acid diester compound.
As described above, the polymer of the present embodiment can be produced by applying a known polymerization method to a raw material composition comprising the compound (A). On the other hand, by employing the method (2) for producing a polymer, a polymer can be obtained without requiring a multi-step process. Further, it is also possible to obtain a molded body by forming a composition (raw material composition) comprising a compound (B) represented by the general formula (III), a polymerizable monomer (C), and at least one phosphorous acid-based ester compound (D) selected from the group consisting of a phosphinous acid ester compound, a phosphonous acid monoester compound, and a phosphorous acid diester compound, and then injecting the raw material composition into a mold to polymerize and cure the raw material composition.
The compound (B) is represented by the following general formula (III).
R21 represents a hydrogen atom or a methyl group, and from the viewpoint of polymerization operability, a methyl group is preferable.
p is an arbitrary integer of 0 to 7, and from the viewpoint of improving the physical properties at the time of heating of the obtained flame-retardant composition, p is preferably 2 to 6, more preferably 3 to 6, and still more preferably 5.
In addition, from the above viewpoint, the compound (B) is preferably a compound represented by the following general formula (IV).
R31 represents a hydrogen atom or a methyl group, and from the viewpoint of polymerization operability, a methyl group is preferable.
In the method (2) for producing a polymer, the addition amount of the compound (B) is not particularly limited. Whereas, from the viewpoint of imparting more sufficient flame retardancy to the polymer and the flame-retardant composition, when the total amount of the raw materials is 100 parts by mass, the addition amount of the compound (B) is preferably 0.1 parts by mass or more, more preferably 3.0 parts by mass or more, and may be 10 parts by mass or more. The upper limit of the addition amount of the compound (B) is not particularly limited. Whereas, from the viewpoint of molding processability, when the total amount of the raw materials is 100 parts by mass, the addition amount of the compound (B) is preferably 50 parts by mass or less, more preferably 40 parts by mass or less, and may be 30 parts by mass or less.
The preferred embodiment of the addition amount of the compound (B) can be read as a preferred embodiment of the content of the compound (B) with respect to 100 parts by mass of the total amount of the raw material composition.
In the method (2) for producing a polymer, the polymerizable monomer (C) to be used is the same as the polymerizable monomer (C) described above, and redundant description is omitted here.
Examples of the phosphinous acid ester compound include diphenylphosphine oxide, diethylphosphine oxide, and dibutylphosphine oxide.
Examples of the phosphonous acid monoester compound include ethyl phenyl phosphinate, butyl phenyl phosphinate, phenyl phenyl phosphinate, and 9,10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide.
Examples of the phosphorous acid diester compound include diethyl phosphite, diisopropyl phosphite, dibutyl phosphite, 1,3-dioxa-2-phosphacyclohexane-2-oxide, 1,3-dioxa-5,5-dimethyl-2-phosphacyclohexane-2-oxide, diphenyl phosphite, bis(2,4-dimethyl)phenyl phosphite, and 1,2,3,4-tetrahydro-1,3-dioxa-2-phosphanaphthalene-2-oxide.
These phosphorous acid-based ester compounds (D) may be used alone, or two or more thereof may be used in combination.
Among these, as the phosphorous acid-based ester compound (D), diethyl phosphite, dibutyl phosphite, diphenyl phosphite, and 9,10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide are preferable, and diethyl phosphite, dibutyl phosphite, and 9,10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide are more preferable, from the viewpoint of raw material mixing property and flame retardancy.
The addition amount of the phosphorous acid-based ester compound (D) is not particularly limited. Whereas, from the viewpoint of imparting more sufficient flame retardancy to the polymer and the flame-retardant composition, when the total amount of the raw materials is 100 parts by mass, the addition amount of the phosphorous acid-based ester compound (D) is preferably 0.1 parts by mass or more, more preferably 3.0 parts by mass or more, may be 10 parts by mass or more, and may be 15 parts by mass or more. Further, the upper limit of the addition amount of the phosphorous acid-based ester compound (D) is not particularly limited. Whereas, from the viewpoint of molding processability, when the total amount of the raw materials is 100 parts by mass, the addition amount of the phosphorous acid-based ester compound (D) is preferably 30 parts by mass or less, and more preferably 25 parts by mass or less.
The preferred embodiment of the addition amount of the phosphorous acid-based ester compound (D) can be read as a preferred embodiment of the content of the phosphorous acid-based ester compound (D) with respect to 100 parts by mass of the total amount of the raw material composition.
In addition, the addition amount of the phosphorous acid-based ester compound (D) with respect to 100 mol % of the compound (B) is not particularly limited. Whereas, from the viewpoint of further improving the flame retardancy, the addition amount of the phosphorous acid-based ester compound (D) with respect to 100 mol % of the compound (B) is preferably 40 mol % or more, more preferably 50 mol % or more, still more preferably 60 mol % or more, and even more preferably 90 mol % or more. Further, from the viewpoint of easily achieving both the improvement of the flame retardancy and the avoidance of elution and bleeding of the phosphorous acid-based ester compound (D), the addition amount of the phosphorous acid-based ester compound (D) with respect to 100 mol % of the compound (B) is preferably 160 mol % or less, and more preferably 150 mol % or less.
The preferred embodiment of the addition amount of the phosphorous acid-based ester compound (D) with respect to 100 mol % of the compound (B) can be read as a preferred embodiment of the content of the phosphorous acid-based ester compound (D) with respect to 100 mol % of the compound (B) in the raw material composition.
In the method (2) for producing a polymer, a radical polymerization initiator (E) may be used. The type of the radical polymerization initiator (E) is not particularly limited, and can be appropriately selected depending on the types of the compound (B), the polymerizable monomer (C), and the phosphorous acid-based ester compound (D). Examples of the radical polymerization initiator (E) include a thermal radical polymerization initiator which generates a radical by heat, and a photoradical polymerization initiator which generates a radical by light.
Examples of the thermal radical polymerization initiator include organic peroxides such as azo compounds such as 2,2′-azobisisobutyronitrile (AIBN) and 2,2′-azobis(2,4-dimethylvaleronitrile) (ADVN); diacyl peroxides such as benzoyl peroxide; peroxyesters such as t-butyl peroxybenzoate; hydroperoxides such as cumene hydroperoxide; dialkyl peroxides such as dicumyl peroxide; ketone peroxides such as methyl ethyl ketone peroxide and acetylacetone peroxide; peroxyketals; alkyl peresters; and percarbonates.
As the photoradical polymerization initiator, a commercially available product can be used. Examples thereof include Irgacure (registered trademark, the same applies hereinafter) 651, Irgacure 184, Irgacure 2959, Irgacure 127, Irgacure 907, Irgacure 369, Irgacure 379, Irgacure 819, Irgacure 784, Irgacure OXE01, Irgacure OXE02, and Irgacure 754 (all manufactured by BASF Corporation). These may be used alone, or two or more thereof may be used in combination.
The addition amount of the radical polymerization initiator (E) is not particularly limited, but in order to obtain a polymer having a sufficient degree of polymerization, when the total amount of the raw materials is 100 parts by mass, the addition amount is preferably 0.001 parts by mass or more, and more preferably 0.001 parts by mass or more and 3 parts by mass or less.
The method (2) for producing a polymer may be carried out using a mold. By carrying out polymerization and curing using a mold, the shape of the mold can be imparted to the polymer, and as a result, a cured product of the polymer having excellent flame retardancy can be obtained. Examples of the mold include a mold composed of a pair of plate-like bodies such as a reinforced glass, a chrome-plated plate, or a stainless steel plate and a gasket such as a soft vinyl chloride resin, and a mold composed of opposed surfaces of a pair of endless belts that travel in the same direction at the same speed and gaskets that travel at the same speed as both endless belts on both side portions thereof.
Further, by injecting a composition to which various additives that can be used for the flame-retardant composition described later are added in addition to the raw material composition of the polymer into the mold, a cured product of a flame-retardant composition comprising a polymer can be obtained in a state in which the shape of the mold is imparted by injecting a composition to which various additives that can be used for the flame-retardant composition described later are added in addition to the raw material composition of the polymer into the mold.
The polymerization temperature is preferably set to two stages of primary curing of 40 to 90° C. and subsequent secondary curing of 110 to 140° C. from the viewpoint of enhancing transparency and polymerization rate.
The flame-retardant composition of the present embodiment comprises a polymer including a structural unit represented by the above-mentioned general formula (I). Since phosphorus atoms are contained in the molecular structure of the polymer, elution, bleeding, or the like of the phosphorus-containing component due to heating does not occur, and the flame-retardant composition can maintain good flame retardancy.
The proportion of the polymer contained in the flame-retardant composition is not particularly limited, but is preferably 0.1 parts by mass or more, and more preferably 1.0 part by mass or more, with respect to 100 parts by mass of the flame-retardant composition, from the viewpoint of flame retardancy. The upper limit of the proportion of the polymer contained in the flame-retardant composition is not particularly limited, but in consideration of molding processability, it is preferably 50 parts by mass or less, and more preferably 30 parts by mass or less.
The flame-retardant composition may comprise various additives such as a diluent, a pigment, a dye, a filler, an ultraviolet absorber, a viscosity improver, a shrinkage reducing agent, an aging inhibitor, a plasticizer, an aggregate, a flame retardant, a stabilizer, a fiber reinforcement, an antioxidant, a leveling agent, and an anti-sagging agent.
The use of the polymer and the flame-retardant composition of the present embodiment is not particularly limited, but they can be suitably used for a sheet, a polymer plate, a molded plate, a coating, a pressure-sensitive adhesive, an adhesive, and the like having particularly flame retardancy.
As a preferred embodiment in which the polymer and the flame-retardant composition of the present embodiment are used, a flame-retardant sheet or a flame-retardant plate may be mentioned. A flame-retardant sheet or a flame-retardant plate obtained by using the polymer and the flame-retardant composition is excellent in that it does not contain harmful halogen atoms and is less likely to cause deterioration in physical properties such as drip at the time of heating.
The flame-retardant sheet and the flame-retardant plate can be processed into an arbitrary three dimensional shape by secondary molding of a known method. Examples of the secondary molding method include vacuum molding and air-pressure molding.
After the flame-retardant sheet or the flame-retardant plate is heated in advance to an appropriate temperature using a heating furnace or the like, the flame-retardant sheet or the flame-retardant plate can be processed into a desired shape by being made to conform to a mold using vacuum, compression, air, mechanical pressure, or a combination thereof.
Hereinafter, the present invention will be described in detail with reference to Examples, but the present invention is not limited to these Examples.
Each compound represented by the following reaction formula was synthesized by the synthesis methods of [Production Example 1] and [Example 1] and then synthesized as the compound (A) represented by the general formula (II), a compound represented by Chemical Formula A-1 in the following reaction formula.
To a nitrogen-purged four-neck flask, 15.00 g (116.99 mmol) of 7-octenol, 26.60 g (122.84 mmol) of 9,10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide, and 100 g of toluene were added, and the mixture was heated to 60° C. Then, 1.27 g (5.85 mmol) of Perbutyl O was added thereto, and the mixture was stirred for 1 hour. The reaction solution was cooled and concentrated to obtain 45.15 g of a solution containing a compound (a1).
To a nitrogen-purged four-neck flask, 40.30 g (116.99 mmol) of the compound (a1) obtained in Production Example 1, 19.53 g (193.03 mmol) of triethylamine, and 200 g of acetonitrile were added, and the mixture was stirred at 10° C. or lower. Then, 14.67 g (140.39 mmol) of methacrylic acid chloride was added dropwise, and the mixture was stirred at room temperature (25° C.) for 2 hours. To the reaction solution were added 81.5 g of ion-exchanged water and 0.13 g of N,N-dimethylaminopyridine, and the mixture was stirred at room temperature. 733.8 g of ethyl acetate was added to the reaction solution to extract an organic layer, and the obtained extract was washed with 672.4 g of 4 wt % hydrochloric acid, 1048.6 g of 6 wt % aqueous solution of sodium hydrogen carbonate, and 587.9 g of saturated brine, and the organic layer was concentrated. The organic layer was dried over sodium sulfate and then purified by silica gel column chromatography to obtain 33.00 g (80.01 mmol, 68.4 mol %) of a compound (A) represented by Chemical Formula A-1. The results of 1H-NMR measurement of the obtained compound (A) are shown below.
1H-NMR (400 MHz, CDCl3, TMS) δ: 7.86 (dd, J=8.0, 4.8 Hz, 1H), 7.82 (dd, J=8.0, 3.2 Hz, 1H), 7.77 (dd, J=8.0, 0.8 Hz, 1H), 7.59 (tt, J=11.6, 0.8 Hz, 1H), 7.41 (tdd, J=7.2, 2.8, 0.8 Hz, 1H), 7.28 (tt, J=7.2, 0.8 Hz, 1H), 7.15 (td, J=7.2, 1.2 Hz, 1H), 7.13 (dd, J=8.0, 0.8 Hz, 1H), 6.00 (dd, J=1.6, 0.8 Hz, 1H), 5.45 (d, J=1.6 Hz, 1H), 4.02 (t, J=6.8 Hz, 2H), 2.00-1.90 (m, J=3.6, 2H), 1.84 (s, 3H), 1.60-1.48 (m, 4H), 1.32-1.14 (m, 8H)
A mixture of the raw materials in Table 1 was added to a beaker containing a stirrer, and stirred until completely dissolved to obtain a raw material composition (raw material liquid). The raw material liquid was injected into a cell composed of two stainless steel plates (2 mm thick, 20 cm square) and a gasket made of a vinyl chloride resin, and was polymerized in a hot water bath at 60° C. for 6 hours and then in an oven at 130° C. for 2 hours, thereby obtaining a sheet having a thickness of 3.2 mm.
A test piece having a length of 127 mm x a width of 13 mm x a thickness of 3.2 mm was cut out from the obtained sheet. Using the test piece, the following combustion test was performed and evaluated. The obtained evaluation results of the combustion test are shown in Table 1.
In Table 1, a blank column indicates no blending. Moreover, Examples 2, 3, and 5 to 9 are examples in which the above-mentioned polymer production method (2) was employed, and Example 4 is an example in which the above-mentioned polymer production method (1) was employed.
A test piece having a thickness of 3.2 mm was allowed to stand in an environment of 23° C. and 50% RH for 18 hours. In accordance with JIS K 6911:1995 A test, a horizontally held test piece was subjected to indirect flaming with a burner for 30 seconds. The average value of three test pieces was taken, and the flame retardancy was evaluated by the rate of combustion (mm/second) of each test piece. As for the combustion rate, the smaller the numerical value, the more excellent the flame retardancy.
In the above-described combustion rate test, it was determined whether or not dripping occurred from the test piece during combustion and drips fell. If dripping did not occur or drips did not fall, it was evaluated as “A”, and if drips fell, it was evaluated as “B”.
The test piece after the completion of the combustion test was visually observed, and when the formation of a black flame-retardant carbonized layer due to the phosphorus-containing component was confirmed, it was evaluated as “Yes”, and when it was not confirmed, it was evaluated as “No”.
The surface of the test piece prepared as described above was observed, and the presence or absence of bleed out (elution, bleeding) of the phosphorus-containing component was determined by visual observation and tactile sense. If the bleed out was not confirmed, it was evaluated as “No”, and if it was confirmed, it was evaluated as “Yes”.
The raw materials in Table 1 are as follows.
Compound (A-1): Compound represented by the above Chemical Formula A-1 obtained by the synthesis methods of [Production Example 1] and [Example 1]
Compound (B-1): 7-octenyl methacrylate (manufactured by Kuraray Co., Ltd.) (compound represented by the following Chemical Formula B-1)
Compound (B-2): allyl methacrylate (2-propenyl methacrylate, AMA) (manufactured by FUJIFILM Wako Pure Chemical Corporation)
MMA: methyl methacrylate (manufactured by Kuraray Co., Ltd.)
DOPO: 9,10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide (manufactured by Tokyo Chemical Industry Co., Ltd.)
Diethyl phosphite: diethyl phosphite (manufactured by FUJIFILM Wako Pure Chemical Corporation)
V-65: 2,2′-azobis(2,4-dimethylvaleronitrile) (manufactured by FUJIFILM Wako Pure Chemical Corporation)
PERHEXA (registered trademark) C: 1,1-di(tert-butylperoxy)cyclohexane (manufactured by NOF Corporation)
From Example 4 in Table 1, the sheet using the polymer including the structural unit represented by the general formula (I) had a low combustion rate, did not cause dripping, had a flame-retardant carbonized layer on the surface, and bleed-out was not confirmed. Thus, it can be seen that Example 4 exhibited excellent flame retardancy.
Further, as in Examples 2, 3 and 5 to 9, the polymers produced by the polymer production method (2) also exhibited excellent flame retardancy as in Example 4.
On the other hand, in the sheet of Comparative Example 1 using the polymer not comprising the structural unit represented by the general formula (I), the drips fell. Further, the sheet of Comparative Example 2 using a polymer not comprising the structural unit represented by the general formula (I) had a high combustion rate, and in addition, no flame-retardant carbonized layer was confirmed. As described above, in Comparative Examples 1 and 2, excellent flame retardancy could not be exhibited.
The polymer of the present invention is excellent in flame retardancy and hardly causes deterioration in physical properties such as softening at the time of heating. Therefore, the polymer of the present invention and the flame-retardant composition containing the polymer can be used for applications requiring flame retardancy, and in particular, can be suitably applied to a flame-retardant sheet, a flame-retardant plate, a flame-retardant paint and a flame-retardant coating, a flame-retardant pressure-sensitive adhesive, a flame-retardant adhesive, a flame-retardant fiber, and the like.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2020-193633 | Nov 2020 | JP | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/JP2021/042345 | 11/17/2021 | WO |
