JP2016017165A - Flame retardant-containing styrene resin composition and production method thereof - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide a technique of molding a styrene resin foam having good external appearance that, even when a polymer type flame retardant is used, not only imparts flame retardancy and environmental friendliness but also prevents the decomposition of the polymer type flame retardant under an extrusion condition.SOLUTION: A flame retardant composition according to the present invention is obtained by kneading a first styrene resin, a brominated styrene-butadiene block polymer, and a stabilizer under conditions where the barrel temperature of an extruder is 180°C or less and the specific energy is 0.50 kWh/kg, and the flame retardant composition has a 5% weight loss temperature measured by thermogravimetric analysis of 255°C or more and 270°C or less.SELECTED DRAWING: None

Description

  The present invention relates to a flame retardant composition used in a styrene resin extruded foam having excellent appearance and further achieving both thermal stability and flame retardancy, and a styrene resin extruded foam using the flame retardant composition. .

  A method of continuously producing a styrene resin extruded foam by melting a styrene resin with an extruder or the like, then adding a foaming agent, cooling, and extruding it into a low pressure region is already known. ing. Since this styrene resin extruded foam needs to satisfy the flammability standard of the extruded styrene foam heat insulating plate described in JIS A9511, it usually contains a flame retardant.

  The flame retardant used in the styrene resin extruded foam is required not to decompose at a temperature around 230 ° C., which is a general styrene resin extrusion process condition. Decomposition of the flame retardant during extrusion causes deterioration of the resin, so the moldability of the resulting styrene resin extruded foam deteriorates or the cell diameter of the styrene resin extruded foam becomes difficult to control. This is because. Further, the flame retardant is required to have a property of being efficiently decomposed at a high temperature before the styrene resin is decomposed. General styrene resin begins to decompose at around 300 ° C, but the flame retardancy of the styrene resin extruded foam can be improved by decomposition of the flame retardant at a temperature lower than the decomposition temperature of the styrene resin. It is. Furthermore, from the viewpoint of product cost and moldability of the resulting styrene resin extruded foam, it is necessary to improve the flame retardancy with a small amount.

  Against this background, hexabromocyclododecane (hereinafter referred to as “HBCD”) has been widely used as a flame retardant used in styrene resin extruded foams. HBCD is known to be relatively stable under extrusion processing conditions, and to be efficiently decomposed at high temperatures before the styrenic resin is decomposed, and can exhibit high flame retardancy even in a small amount. However, HBCD is not preferable in terms of environmental hygiene because it is hardly decomposable and exhibits high accumulation.

  Therefore, as a flame retardant to replace HBCD, a polymer type flame retardant has been proposed in place of the conventional low-molecular flame retardant (Patent Documents 1 and 2). However, this polymer-type flame retardant has a problem in thermal stability, and even under general styrene resin extrusion conditions, thermal decomposition / thermal degradation may cause discoloration, which may cause poor appearance of the foam. .

  By the way, as a method of forming a foam by blending a polymer flame retardant with a styrene resin, a method of directly adding to a styrene resin and extrusion foaming (Patent Document 2), first blending with a styrene resin and concentrating. A method (Patent Document 1) is known in which a product pellet is prepared and then mixed with a styrene resin pellet to form a foam. However, the appearance of the foam obtained in Patent Document 1 is not clear.

International Publication No. 2007/058736 International Publication No. 2010/080285

  The present invention has been made in view of the above circumstances, and the purpose thereof is not only to impart flame retardancy and environmental compatibility, but also to the use of extrusion processing conditions when a polymer-type flame retardant is used. An object of the present invention is to provide a molding technology for a styrene resin foam which prevents decomposition of a polymer flame retardant and has a good appearance.

As a result of intensive studies to solve the above problems, the inventors of the present invention have prepared a flame retardant composition by kneading a polymer-type flame retardant together with a styrene resin and a stabilizer in advance. By appropriately controlling the specific energy to be applied, the thermal stability of the flame retardant composition can be improved, and such a flame retardant composition is further blended with a styrene resin and a foaming agent to form a foam. The present inventors have found that a styrene resin extruded foam having excellent flame retardancy and good appearance can be obtained, thereby completing the present invention.
That is, the flame retardant composition of the present invention comprises a first styrenic resin, a brominated styrene-butadiene block polymer, and a stabilizer having an extruder barrel temperature of 180 ° C. or less and a specific energy of 0.50 kWh / kg or less. It is characterized by being obtained by kneading under conditions, and having a 5% weight loss temperature by thermogravimetric analysis of 255 ° C. or more and 270 ° C. or less. The flame retardant composition of the present invention is preferably obtained by kneading with an extruder having a ratio (L / D) of the effective length L to the outer diameter D of 52 or less. It is preferably obtained by kneading with an extruder having a discharge amount per rotation (Q / N) of 0.6 kg / Hr / rpm or more.
Furthermore, the flame retardant composition of the present invention is 20 parts by weight or more and 200 parts by weight or less of the first styrenic resin and 5 parts by weight of the stabilizer with respect to 100 parts by weight of the brominated styrene-butadiene block polymer. The content is preferably 75 parts by weight or less. The stabilizer is preferably at least one selected from the group consisting of an epoxy compound, a phenol stabilizer, a phosphite stabilizer, and a polyhydric alcohol partial ester.

  Furthermore, a styrene resin extruded foam obtained by extrusion foaming a mixture containing the flame retardant composition of the present invention, the second styrene resin, and a foaming agent is also included in the technical scope of the present invention. . It is preferable that the mixture further contains a second stabilizer.

  Since the flame retardant composition of the present invention is produced by kneading a styrene resin, a brominated styrene-butadiene block polymer, and a stabilizer under a predetermined temperature and specific energy condition, its thermal stability is low. It is good. Further, by blending this flame retardant composition with a styrene resin and a foaming agent to obtain a foam, a styrene resin extruded foam having excellent flame retardancy and good appearance can be obtained.

1. Flame retardant composition The flame retardant composition of the present invention kneads (melts) a first styrene resin, a brominated styrene-butadiene block polymer, and a stabilizer in a state where the brominated styrene-butadiene block polymer is softened. It is a pellet-like composition produced by mixing (including kneading), the kneading temperature is adjusted low, and the work amount during kneading is controlled within a certain range, so it has excellent thermal stability. It will be. Moreover, since this flame retardant composition acts as a masterbatch and has improved thermal stability while containing a flame retardant at a high concentration, a styrene-based resin extruded foam (hereinafter referred to as the styrene resin extruded foam) obtained using this flame retardant composition. The “foam” and “styrene resin foam” may be simply referred to), which can achieve both thermal stability and flame retardancy, and also has a good appearance.

  For the kneading, an extruder can be used, preferably a twin screw extruder, more preferably a same direction twin screw extruder. The above raw materials are supplied to such an extruder, the heating temperature (barrel temperature) of the barrel part (cylinder part) of the extruder is controlled within a certain range, and the screw is rotated inside the barrel part (cylinder part). To knead the raw materials. The barrel temperature of the extruder is 180 ° C. or lower, preferably 170 ° C. or lower, more preferably 160 ° C. or lower. Lowering the barrel temperature of the extruder can prevent overheating during kneading. Moreover, it is preferable that an extruder barrel temperature is 130 degreeC or more, More preferably, it is 140 degreeC or more. When the extruder barrel temperature is within this range, it can be stably softened.

  The work amount during kneading can be evaluated by specific energy (a value obtained by dividing the work amount of the extruder by the discharge amount Q per unit time). Usually, the larger the specific energy, the better the kneading efficiency. In the present invention, however, the specific energy is intentionally suppressed, so that the brominated styrene-butadiene block polymer is hardly decomposed and the thermal stability of the flame retardant composition is good. To find out. The specific energy is 0.50 kWh / kg or less, preferably 0.45 kWh / kg or less, more preferably 0.40 kWh / kg or less, and still more preferably 0.38 kWh / kg or less. The lower limit of the specific energy can be appropriately set as long as kneading is possible, and is, for example, about 0.1 kWh / kg or more, preferably about 0.2 kWh / kg or more.

  The specific energy can be adjusted by the ratio (L / D) between the effective length L and the outer diameter D of the extruder screw and the discharge amount (Q / N) per one screw rotation.

  The ratio of the effective length L of the extruder screw to the outer diameter D (L / D) is a numerical value that serves as a guide for the kneading efficiency of the extruder screw. The larger this value, the greater the work during kneading. Specific energy increases. In the present invention, from the viewpoint of intentionally suppressing the specific energy, the ratio (L / D) between the effective length L and the outer diameter D of the extruder screw is preferably 52 or less, more preferably 50 or less, and still more preferably. 45 or less. The ratio (L / D) between the effective length L and the outer diameter D is preferably 15 or more, more preferably 20 or more, and further preferably 25 or more. When the ratio (L / D) of the effective length L to the outer diameter D is within this range, the raw material of the flame retardant composition can be sufficiently kneaded.

  Further, the discharge amount (Q / N) per rotation of the screw represents the quantitative efficiency of the extruder, and the larger this value, the less the work during kneading and the lower the specific energy. For this reason, the discharge amount (Q / N) per screw rotation is preferably 0.6 kg / Hr / rpm or more, more preferably 0.8 kg / Hr / rpm or more. Further, the discharge amount (Q / N) per rotation of the screw is preferably 3 kg / Hr / rpm or less, more preferably 2.5 kg / Hr / rpm or less. When the discharge amount per rotation is within this range, the raw material of the flame retardant composition can be sufficiently kneaded.

  From the viewpoint of adjusting the discharge amount per screw rotation to the above range, the screw rotation speed N is preferably 50 rpm or more, more preferably 70 rpm or more, preferably 250 rpm or less, more preferably 200 rpm or less. Further, the discharge amount Q is preferably 30 kg / hr or more, more preferably 40 kg / hr or more, preferably 500 kg / hr or less, more preferably 400 kg / hr or less.

A flame retardant composition is obtained by kneading the raw materials under the above conditions, but the obtained flame retardant composition may be granulated into pellets by a method such as underwater cut, hot cut, strand cut, etc. preferable. Especially, the strand cut which extrudes a flame retardant composition from a die | dye in the shape of a string, and cut-molds is more preferable. The die is usually circular, and the die diameter is preferably 30 to 90 mm, more preferably 40 to 75 mm.
At this time, the resin temperature at the die outlet is preferably 215 ° C. or lower, more preferably 200 ° C. or lower, and particularly preferably 198 ° C. or lower. However, the resin temperature need not be lowered to this preferred range. Since the flame retardant composition of the present invention is obtained by adjusting the extruder barrel temperature and specific energy within a predetermined range and kneading, even if the resin temperature at the die outlet is high (for example, 200 ° C. or higher, or 210 ° C. or higher), the thermal stability is improved. The lower limit of the die outlet temperature may be 180 ° C. or higher, preferably 190 ° C. or higher.

  The first styrene resin used in the flame retardant composition is not particularly limited, and any styrene polymer can be used. Moreover, this styrenic polymer may be used independently and the blended material mixed with the other polymer may be sufficient. Furthermore, either virgin resin or recycled resin may be used.

  The styrene polymer is styrene; methyl styrene (vinyl toluene), α-methyl styrene, β-methyl styrene, ethyl styrene, α-ethyl styrene, β-ethyl styrene, isopropyl styrene, dimethyl styrene (vinyl xylene), etc. Styrene substituted with an alkyl group having 1 to 5 carbon atoms; halogen-substituted styrene such as bromostyrene and chlorostyrene; homopolymers or copolymers of styrene monomers such as; This copolymer may be a copolymer of two or more styrene monomers, or a copolymer of a styrene monomer and another monomer. Other monomers used here include divinylbenzene; olefinic monomers such as butadiene; (meth) acrylic monomers such as acrylic acid, methacrylic acid, methyl acrylate, methyl methacrylate, and acrylonitrile; And carboxylic acid anhydrides such as maleic anhydride and itaconic anhydride. The other monomer can be used as long as the mechanical properties such as compression strength of the styrene resin extruded foam are not deteriorated.

  The weight average molecular weight of the styrenic polymer is preferably 100,000 or more and 500,000 or less, more preferably 150,000 or more and 400,000 or less, still more preferably 200,000 or more, 350,000 or less. The smaller the weight average molecular weight, the easier it is to lower the specific energy and the higher the heat resistance of the flame retardant composition. Further, in the present invention, since the extruder barrel temperature and specific energy are adjusted, even if the weight average molecular weight of the styrene polymer is high (for example, 210,000 or more, or 300,000 or more), the flame retardant composition. It can be a thing.

  Examples of the other polymer used in the blend include a polymer obtained by polymerizing the other monomer; rubber reinforced styrene such as diene rubber reinforced polystyrene and acrylic rubber reinforced polystyrene. The blend ratio of the styrene polymer and the other polymer (styrene polymer / other polymer) is, for example, preferably 0.01 to 100, and more preferably 0.5 to 3.

  Among these styrenic resins, styrenic polymers are preferable from the viewpoint of extrusion foaming moldability and the like, more preferably homopolymers of styrene monomers such as styrene homopolymers; styrene-acrylonitrile copolymers, ( A copolymer of a styrene monomer such as (meth) acrylic acid copolymerized polystyrene, maleic anhydride-modified polystyrene, impact-resistant polystyrene (for example, acrylonitrile-butadiene-styrene copolymer) and other monomers; And more preferably a homopolymer of a styrene monomer, and particularly preferably a styrene homopolymer from the viewpoint of cost.

  The recycled styrene resin is not particularly limited as long as it is a recycled product containing the styrene resin, and examples thereof include a recycled styrene resin obtained by recycling a foamed polystyrene product. Examples of the expanded polystyrene products used in the recycled styrene resin include styrene resin foams such as fish box EPS (expanded polystyrene), household appliance cushioning materials, food expanded polystyrene trays, and polystyrene trays as refrigerator interior materials. Can be mentioned. Moreover, the cut waste generated in the finish cutting process of the product and the foam obtained by recycling the scrap generated at the start-up of the extrusion operation can be used as the recycled styrene resin.

  The recycled styrene-based resin may be put into the extruder as it is, but it is generally preferable to reduce the volume and / or process (pelletize) so as to be easily put into the extruder. In the processing (pelletization), kneading (including melt kneading) is generally performed by an extruder, and the temperature at which molecular degradation of the resin is suppressed as much as possible including the influence of a flame retardant, for example, It is preferable to knead at about 160 to 240 ° C. Further, it is desirable to provide a vent port in the extruder in order to degas the foaming agent in the recycled styrene resin.

  As the first styrenic resin in the present invention, one having a melt flow rate (hereinafter referred to as “MFR”) of 1 to 15 g / 10 min is preferably used. When the MFR is in this range, the molding processability at the time of extrusion foam molding is excellent, and the discharge amount at the time of molding process, the thickness, width, density or closed cell ratio of the obtained thermoplastic resin foam is a desired value. Styrene resin with excellent foaming properties (further foaming properties are better as the thickness, width, density, closed cell ratio, surface properties, etc. of the foam are easily adjusted to desired conditions) and appearance. A foam is obtained. The resulting styrene resin extruded foam has a balance of mechanical strength such as compressive strength, bending strength or bending deflection, and properties such as toughness. Further, the MFR of the first styrenic resin is more preferably 4 to 12 g / 10 min in order to suppress as much as possible the shearing heat generated during kneading in the extruder. The MFR in the present invention is a value measured according to JIS K7210.

  In addition, the first styrene resin has a branched structure, so that the MFR, the viscosity at the time of molding, the tension, and the like can be adjusted. For example, in a styrene resin, a branched structure can be formed by using a bifunctional monomer such as divinylbenzene; an olefin monomer such as butadiene; and the longer the branched chain, the higher the MFR, viscosity, and tension. There is a tendency to grow.

  The first styrene-based resin is preferably 20 parts by weight or more and 60 parts by weight or less, more preferably 30 parts by weight or more and 50 parts by weight or less, in 100 parts by weight of the flame retardant composition. The first styrenic resin is preferably 60 parts by weight or more and 120 parts by weight or less, more preferably 70 parts by weight or more, 100 parts by weight with respect to 100 parts by weight of a brominated styrene-butadiene block polymer described later. Parts by weight or less (particularly less than 100 parts by weight). The more the first styrenic resin, the better the mechanical strength of the resulting flame retardant composition, and the better the flame retardancy when the first styrenic resin is in this range.

  The flame retardant composition also contains a brominated styrene-butadiene block polymer as described above. This brominated styrene-butadiene block polymer acts as a flame retardant, and by using this, a foam excellent in flame retardancy and environmental compatibility can be obtained.

  The brominated styrene-butadiene block polymer is a block copolymer having a styrene block and a brominated butadiene block, and is excellent in flame retardancy, cost, and supply stability. The number of blocks of the brominated styrene-butadiene block polymer is preferably 2 to 10, for example, and more preferably 2 to 5. The number of blocks is preferably an odd number. In this case, the terminal block is preferably a styrene block from the viewpoint of good mixing with the styrene resin. The bromine content of the brominated styrene-butadiene block polymer is preferably 50% by weight to 80% by weight, more preferably 60% by weight to 70% by weight.

  The weight average molecular weight of the brominated styrene-butadiene block polymer is preferably 50,000 to 300,000, more preferably 70,000 to 200,000. Furthermore, the 5% weight loss temperature of the brominated styrene-butadiene block polymer is preferably 240 ° C. or higher, more preferably 250 ° C. or higher, further preferably 260 ° C. or higher, and preferably 280 ° C. or lower. It is more preferable that the temperature is 270 ° C. or lower.

  The content of brominated styrene-butadiene polymer is preferably 30% by weight or more and 80% by weight or less in 100% by weight of the flame retardant composition, more preferably 40% by weight or more, and 45% by weight or more. More preferably. As the brominated styrene-butadiene block polymer content is increased, the amount of the flame retardant composition added can be reduced when preparing a styrene resin extruded foam, which is advantageous in terms of cost. Further, the lower the content of brominated styrene-butadiene block polymer, the better the mechanical strength of the flame retardant composition.

  The flame retardant composition of the present invention further contains a stabilizer. By using the stabilizer, the thermal stability of the obtained flame retardant composition is improved. Stabilizers include epoxy compounds, polyhydric alcohol partial esters, phenolic stabilizers, phosphite stabilizers, hindered amine stabilizers, among others, epoxy compounds, polyhydric alcohol partial esters, phenolic stabilizers. Agents and phosphite stabilizers are preferred. Stabilizers may be used alone or in combination, but are preferably used in combination of two or more.

  As the chemical structure of the epoxy compound used in the present invention, for example, a compound in which an epoxy group (such as a glycidyl group) is bonded to both ends of an aromatic ring-containing unit (such as bisphenols or phenols) having a repeating number of 1 or more is used. From the aspect of cost, performance, and supply stability, structural formula (1)

Bisphenol A diglycidyl ether type epoxy resin represented by the structural formula (2)

Cresol novolac type epoxy resin represented by the structural formula (3)

A phenol novolac type epoxy resin represented by
Structural formula (4)

The epoxy compound may be partially halogenated, such as a brominated bisphenol A diglycidyl ether type epoxy resin represented by: These epoxy compounds may be used alone or in combination of two or more.

  The epoxy compound preferably has an epoxy equivalent of less than 1000 g / eq. It is thought that the epoxy group suppresses the decomposition of the brominated flame retardant and improves the thermal stability performance of the styrene resin, so that suppressing the epoxy equivalent effectively suppresses the decomposition of the flame retardant, It is also advantageous in terms of cost. For this reason, the epoxy equivalent is more preferably less than 500 g / eq, more preferably less than 400 g / eq, and preferably 180 g / eq or more.

The epoxy compound is preferably 4 parts by weight or more and 20 parts by weight or less, and more preferably 4 parts by weight or more and 10 parts by weight or less with respect to 100 parts by weight of the brominated styrene-butadiene block polymer. As the epoxy compound content increases, decomposition of the brominated styrene-butadiene block polymer and styrene resin is suppressed, and as a result, enlargement of the cell diameter (bubble diameter) forming the styrene resin extruded foam can be suppressed. The heat insulation performance can be improved. Further, by suppressing the decomposition of the styrene resin, the molecular weight distribution can be maintained, and the moldability and the smoothness of the foam surface can be maintained. Furthermore, since decomposition | disassembly of a flame retardant can also be suppressed, the blackening of another additive and a styrene resin can be prevented, and the external appearance of a styrene resin extrusion foam becomes favorable. In addition, when the content of the epoxy compound is in the above range, the flame retardant can be appropriately stabilized. Therefore, the flame retardant can be effectively decomposed when the styrene resin extruded foam is burned, and the flame retardancy is improved.
Moreover, it is preferable that an epoxy compound is 10 to 50 weight% in 100 weight% of stabilizers, More preferably, it is 20 to 40 weight%.

The polyhydric alcohol partial ester is a mixture of partial esters obtained by reacting a polyhydric alcohol and a carboxylic acid, and has one or more hydroxyl groups in the molecule. Moreover, the mixture of the polyhydric alcohol partial ester may contain the raw material polyhydric alcohol.
The valence of the polyhydric alcohol is preferably 2 to 10, more preferably 4 to 8, and still more preferably 4 to 6. Specific examples of the polyhydric alcohol include tetravalent alcohols such as pentaerythritol; hexavalent alcohols such as dipentaerythritol; octavalent alcohols such as tripentaerythritol; and the like. Examples of the carboxylic acid include monovalent carboxylic acids having 2 to 4 carbon atoms such as acetic acid and propionic acid; divalent carboxylic acids such as adipic acid and glutamic acid; and the like. Divalent carboxylic acids are preferable. .

  As the polyhydric alcohol partial ester, a partial ester of dipentaerythritol and adipic acid or a partial ester of pentaerythritol and adipic acid is preferable. As a partial ester of pentaerythritol or dipentaerythritol and adipic acid, for example, Ajinomoto Fine Techno Co., Ltd., Pleniser (registered trademark) ST-210, Plenizer (registered trademark) ST-220, etc. Can be mentioned.

When the polyhydric alcohol partial ester is included, the content thereof is preferably 0.1 parts by weight or more and 20 parts by weight or less with respect to 100 parts by weight of the brominated styrene-butadiene block polymer, and 0.5 parts by weight. More preferably, it is 10 parts by weight or less. When the content of the polyhydric alcohol partial ester is within this range, the flame retardancy of the flame retardant can be exhibited together with the heat stabilizing effect.
The polyhydric alcohol partial ester is preferably 0% by weight or more and 15% by weight or less, and more preferably 10% by weight or less, in 100% by weight of the stabilizer.

  The phenol-based stabilizer is not particularly limited, and a commercially available substance can be used. Specific examples include triethylene glycol-bis-3- (3-tert-butyl-4-hydroxy-5-methylphenyl) propionate, pentaerythritol tetrakis [3- (3 ′, 5′-di-tert-butyl- 4'-hydroxyphenyl) propionate], octadecyl 3- (3,5-di-tert-butyl-4-hydroxyphenyl) propionate, and these may be used alone or in combination of two or more. You may do it. Among these, pentaerythritol tetrakis [3- (3 ′, 5′-di-tert-butyl-4′-hydroxyphenyl) propionate] is preferably used in terms of price and performance.

The content of the phenol-based stabilizer is preferably 4 parts by weight or more and 20 parts by weight or less, and preferably 7 parts by weight or more and 15 parts by weight or less with respect to 100 parts by weight of the brominated styrene-butadiene block polymer. More preferred. As the amount of the phenol-based stabilizer is larger, the thermal stability of the flame retardant can be improved, and when the content of the phenol-based stabilizer is in the above range, the foam formation of the foam is not affected. The enlargement of the cell diameter is suppressed, and the moldability and heat insulation can be easily controlled.
The phenol-based stabilizer is preferably 30% by weight or more and 80% by weight or less, more preferably 40% by weight or more and 70% by weight or less, in 100% by weight of the stabilizer.

  Examples of the phosphite stabilizer include 3,9-bis (2,4-di-tert-butylphenoxy) -2,4,8,10-tetraoxa-3,9-diphosphaspiro [5.5] undecane. 3,9-bis (2,6-di-tert-butyl-4-methylphenoxy) -2,4,8,10-tetraoxa-3,9-diphosphaspiro [5.5] undecane, and tetrakis (2, 4-di-tert-butyl-5-methylphenyl) -4,4′-biphenylenediphosphonite) is preferred. By using these phosphite stabilizers, the thermal stability of the foam can be improved without reducing the flame retardancy of the foam.

When the phosphite stabilizer is included, the content thereof is preferably 0.1 parts by weight or more and 2.0 parts by weight or less, more preferably 100 parts by weight of the brominated styrene-butadiene block polymer. 0.2 parts by weight or more and 0.9 parts by weight or less. When the content of the phosphite stabilizer is within this range, the flame stability of the flame retardant itself can be maintained while improving the thermal stability of the flame retardant.
Further, the phosphite stabilizer is preferably 1% by weight or more and 8% by weight or less, more preferably 2% by weight or more and 6% by weight or less, in 100% by weight of the stabilizer.

  Examples of the hindered amine stabilizer include bis (2,2,6,6-tetramethyl-4-piperidinyl) decanoate and bis (1,2,2,6,6-pentamethyl) decanedioate. -4-piperidinyl), bis (2,2,6,6-tetramethyl-1) (octyloxy-4-piperidinyl), tetrakis (2,2,6,6-tetramethyl-4-piperidyl)- 1,2,3,4-butanetetracarboxylate is preferred.

  When the hindered amine stabilizer is included, the content is preferably 0.1 parts by weight or more and 2.0 parts by weight or less, more preferably 100 parts by weight of the brominated styrene-butadiene block polymer. Is 0.1 parts by weight or more and 0.9 parts by weight or less. When the content of the hindered amine stabilizer is within this range, the flame stability of the flame retardant itself can be maintained while improving the thermal stability of the flame retardant.

The flame retardant composition thus obtained is excellent in thermal stability, and can increase the 5% weight loss temperature, for example. The 5% weight loss temperature is a value measured by thermogravimetric analysis. When the temperature is raised from room temperature (about 25 ° C.) to 400 ° C. at a rate of 10 ° C./min, the weight of the sample at 150 ° C. is measured. As a reference, it means the temperature at which the weight of the sample has been reduced by 5%. The 5% weight reduction temperature of the flame retardant composition of the present invention is, for example, 255 ° C. or higher, preferably 258 ° C. or higher, more preferably 260 ° C. or higher. The higher the 5% weight loss temperature, the more difficult the flame retardant decomposes and deteriorates when producing a polystyrene resin extruded foam using this flame retardant composition. In addition to facilitating control of the (bubble diameter), it is possible to suppress changes in color due to deterioration of the flame retardant, and it is also possible to suppress foreign substances in the foam. When the 5% weight loss temperature is preferably 290 ° C. or less, more preferably 280 ° C. or less, and further preferably 270 ° C. or less, flame retardancy is efficiently exhibited, which is advantageous in terms of cost.
Moreover, since the flame retardant composition of the present invention is prepared by suppressing the specific energy at the time of kneading, it has an excellent appearance, and for example, discoloration such as black stripes is suppressed. In addition, since the embrittlement is also suppressed, the shape when pelletized is also excellent.

2. Styrenic resin extruded foam The flame retardant composition (such as pellets) is mixed with the second styrenic resin and the foaming agent, and this mixture is extruded and foamed to obtain a styrene resin extruded foam. be able to. By preparing a flame retardant composition (such as pellets) in advance, the flame retardant can be uniformly mixed. And in this invention, since the flame retardant composition which is excellent in thermal stability is mixed uniformly, the obtained styrene resin extruded foam is remarkably excellent in thermal stability and the appearance is also very good.

  As the second styrenic resin, the same as the first styrenic resin can be preferably exemplified. The second styrenic resin may be the same as or different from the first styrenic resin, but is preferably the same.

  The flame retardant composition is preferably 0.5 parts by weight or more, more preferably 3 parts by weight or more with respect to a total of 100 parts by weight of the first styrene resin and the second styrene resin. More preferably, it is 4 parts by weight or more. The greater the amount of the flame retardant composition, the better the thermal stability of the resulting styrene resin extruded foam. The flame retardant composition is preferably 10 parts by weight or less, more preferably 8 parts by weight or less, and still more preferably 7 parts by weight or less with respect to 100 parts by weight of the styrene resin. When the amount of the flame retardant composition is within this range, the obtained styrene resin extruded foam has good flame retardancy.

  Further, the brominated styrene-butadiene block polymer is preferably adjusted to be 1 part by weight or more and 10 parts by weight or less, more preferably 100 parts by weight in total of the first and second styrenic resins. 2 parts by weight or more and 5 parts by weight or less.

The second styrenic resin is preferably 500 parts by weight or more, more preferably 2000 parts by weight or more, still more preferably 3000 parts by weight or more with respect to 100 parts by weight of the first styrenic resin. The amount is preferably 6000 parts by weight or less, more preferably 4000 parts by weight or less.
Further, in 100 wt% of the mixture containing the flame retardant composition (such as pellets), the second styrenic resin, and the foaming agent, the styrenic resin is preferably 75 wt% or more and 99 wt% or less, more preferably. Is 85% by weight or more and 95% by weight or less.

  As the foaming agent used in the present invention, known foaming agents can be appropriately used. For example, organic foaming agents such as saturated hydrocarbons, alcohols, ethers, ketones, esters, halogenated alkyls, halogenated alkenyls; Any of inorganic foaming agents such as water, carbon dioxide and nitrogen; and chemical foaming agents such as azo compounds and tetrazole can be used. However, depending on various properties of the foam, such as the desired foaming ratio and flame retardancy, the amount used may be limited, which may affect the extrusion foamability.

  More preferably, the blowing agent contains at least a saturated hydrocarbon. Thereby, the outstanding environmental compatibility can be provided. Also, in combination with saturated hydrocarbons, other organic foaming agents such as alcohols, ethers and alkyl halides; inorganic foaming agents such as water, carbon dioxide and nitrogen; As a result, the extrusion pressure can be reduced and the foam can be stably produced. Other organic foaming agents combined with saturated hydrocarbons include, from the viewpoint of foamability and foam formability, saturated alcohols having 1 to 4 carbon atoms, ethers having 2 to 4 carbon atoms, and halogens having 1 to 2 carbon atoms. Alkyl chloride is preferred, and ethers having 2 to 4 carbon atoms are more preferred, and dimethyl ether is particularly preferred from the viewpoint of plasticizing effect. Moreover, as an inorganic foaming agent combined with a saturated hydrocarbon, water and carbon dioxide are preferable from the viewpoint of the combustibility of the foaming agent, the flame retardancy of the foam, and the heat insulation, and heat insulation by controlling the cell diameter (bubble diameter). Water is particularly preferable from the viewpoint of improving the performance.

  The saturated hydrocarbon preferably has 3 to 5 carbon atoms, more preferably 3 to 4 carbon atoms, and particularly preferably 4 carbon atoms. Examples of the saturated hydrocarbon include saturated hydrocarbons having 3 carbon atoms such as propane; saturated hydrocarbons having 4 carbon atoms such as n-butane and i-butane; and carbon numbers such as n-pentane, i-pentane and neopentane. 5 saturated hydrocarbons; and the like. These may be used alone or in combination of two or more. Among these, from the viewpoint of foaming properties, saturated hydrocarbons having 3 carbon atoms such as propane; saturated hydrocarbons having 4 carbon atoms such as n-butane and i-butane; and mixtures thereof are preferable. Further, from the viewpoint of the heat insulating performance of the foam, saturated hydrocarbons having 4 carbon atoms such as n-butane and i-butane; mixtures thereof are preferred, and i-butane is particularly preferred.

  In addition, it is preferable that the said saturated hydrocarbon is 2.0 to 5.0 weight part with respect to 100 weight part of styrene resin from a viewpoint of the heat conductivity improvement of a foam. The more saturated hydrocarbons, the easier the control of the cell diameter (bubble diameter) and the better the thermal conductivity of the resulting styrene resin extruded foam. However, when the carbon number of the saturated hydrocarbon becomes small, the property becomes a combustible gas. From the viewpoint of maintaining the flame retardancy of the foam, the saturated hydrocarbon is composed of the first styrenic resin and the second styrenic resin. It is preferable that the amount is 2.7 parts by weight or more and 3.7 parts by weight or less with respect to 100 parts by weight of the total amount of the styrene resin.

  Further, the saturated hydrocarbon is preferably 30% by weight or more and 80% by weight or less, more preferably 40% by weight or more and 70% by weight or less, in the total 100% by weight of the foaming agent. When the amount of the saturated hydrocarbon is within this range, the control of the cell diameter (bubble diameter) is facilitated, and the flame retardancy of the foam is also improved.

  As the alcohols, saturated alcohols are preferable. Moreover, it is preferable that it is C1-C6, More preferably, it is C1-C5, More preferably, it is C1-C4. Specific examples of the alcohols include saturated alcohols having 3 carbon atoms such as methanol; ethanol; propyl alcohol, i-propyl alcohol; 4 carbon atoms such as butyl alcohol, i-butyl alcohol, and t-butyl alcohol. Of saturated alcohols; and the like.

  Examples of the ethers include chain or cyclic ethers, preferably having 2 to 10 carbon atoms, more preferably 2 to 6 carbon atoms, and even more preferably 2 to 4 carbon atoms. Examples of the ethers include chain ethers having 2 carbon atoms such as dimethyl ether (methyl ether); chain ethers having 3 carbon atoms such as methyl ethyl ether; chain chains having 4 carbon atoms such as diethyl ether (ethyl ether). Ethers; chain ethers of oxygen 6 such as diisopropyl ether (isopropyl ether); chain ethers of carbon number 8 such as n-butyl ether; cyclic ethers of carbon number 4 such as furan and tetrahydrofuran; furfural, 2- And cyclic ethers having 5 carbon atoms such as methylfuran and tetrahydropyran.

  As said ketones, chain | strand-shaped ketones are mentioned, As for carbon number, 2-8 are preferable, More preferably, it is 2-6, More preferably, it is C2-C4. Specific examples of the ketones include chain ketones having 2 carbon atoms such as dimethyl ketone; chain ketones having 3 carbon atoms such as methyl ethyl ketone, and carbon atoms having 4 carbon atoms such as diethyl ketone and methyl n-propyl ketone. Chain ketones; C5-chain ketones such as methyl-n-butyl ketone, methyl-i-butyl ketone, and ethyl-n-propyl ketone; C6 such as methyl-n-amyl ketone and ethyl-n-butyl ketone Chain ketones having 7 carbon atoms such as methyl-n-hexyl ketone; and the like.

  As the esters, carboxylic acid esters are preferable, esters of carboxylic acids having 1 to 3 carbon atoms are preferable, and formic acid esters and propionic acid esters are more preferable. Moreover, it is preferable that carbon number is 2-8, More preferably, it is C2-C6. Specific examples of the esters include esters having 2 carbon atoms such as methyl formate; esters having 3 carbon atoms such as ethyl formate; esters having 4 carbon atoms such as propyl formate and methyl propionate. C5 esters such as butyl formate and ethyl propionate; C6 esters such as amyl formate; and the like.

  Examples of the alkyl halides include alkyl fluoride, alkyl chloride, alkyl bromide, alkyl iodide and the like, and alkyl chloride is preferable. Moreover, 1-5 are preferable and C1-C2 is more preferable. Examples of the alkyl halide include alkyl chlorides such as methyl chloride and ethyl chloride.

  Examples of the alkenyl halide include alkenyl fluoride, alkenyl chloride, alkenyl bromide, alkenyl iodide, and the like, and alkenyl fluoride is preferable. Moreover, C1-C5 is preferable and C2-C4 is more preferable. Examples of the alkenyl halide include trans-1,3,3,3-tetrafluoroprop-1-ene.

  Moreover, as said inorganic foaming agent, water and a carbon dioxide are preferable and water is especially preferable.

  In the present invention, when water is used as another foaming agent, it is preferable to add a water-absorbing substance in order to stably perform extrusion foam molding. Specific examples of the water-absorbing substance used in the present invention include hydroxyethyl cellulose, polyacrylate polymer, starch-acrylic acid graft copolymer, polyvinyl alcohol polymer, vinyl alcohol-acrylate copolymer. Water-absorbing polymers such as ethylene-vinyl alcohol copolymer, acrylonitrile-methyl methacrylate-butadiene copolymer, polyethylene oxide copolymer and derivatives thereof; anhydrous silica having a silanol group on the surface (silicon oxide) ) [For example, AEROSIL (registered trademark) manufactured by Nippon Aerosil Co., Ltd. is commercially available] or the like; fine powder having a particle size of 1000 nm or less on the surface; water absorption such as smectite, swellable fluorinated mica Water-swellable layered silicates and their organically treated products; Ito, activated carbon, alumina, silica gel, porous glass, activated clay, diatomaceous earth, or a porous material such as these acid-treated product; and the like. As the water-absorbing substance, a porous substance is preferable, and an acid-treated product of activated clay is particularly preferable. As the acid-treated product of activated clay, for example, Carplex (registered trademark) BS304, Carplex (registered trademark) BS304F, Carplex (registered trademark) # 67, # 80, etc., manufactured by Evonik Degussa Japan can be used.

  The addition amount of the water-absorbing substance in the present invention is appropriately adjusted depending on the addition amount of water and the like, but is preferably 0.01 parts by weight or more and 5 parts by weight or less with respect to 100 parts by weight of the styrenic resin. 0.1 parts by weight or more and 3 parts by weight or less is more preferable. The water-absorbing substance is preferably 1 part by weight or more and 200 parts by weight or less, more preferably 10 parts by weight or more and 70 parts by weight or less with respect to 100 parts by weight of water.

  The amount of the blowing agent used is preferably 2 parts by weight or more and 20 parts by weight or less, and more preferably 4 parts by weight or more and 10 parts by weight or less with respect to 100 parts by weight of the total of the first and second styrenic resins. The greater the amount of foaming agent used, the higher the foaming ratio, and the easier it is to exhibit properties such as light weight and heat insulation as a resin foam, and when the amount of foaming agent used is within this range, Since the amount is appropriate, defects such as voids generated in the foam can be suppressed.

  The total content of the flame retardant composition (such as pellets), the second styrenic resin, and the foaming agent in the mixture subjected to extrusion foaming is preferably 85% by weight or more in 100% by weight of the mixture. More preferably, it is 90% by weight or more and preferably 99% by weight or less.

  In this invention, you may add a heat ray radiation inhibitor as needed. The heat ray radiation inhibitor can improve the heat insulation of the foam, and a foam having high heat insulation can be obtained. Here, the heat ray radiation inhibitor refers to a substance having a characteristic of reflecting, scattering, and absorbing light in the near infrared or infrared region (for example, a wavelength region of about 800 to 3000 nm).

  Examples of the heat ray radiation suppressor include carbon materials such as graphite and carbon black; metal pastes such as aluminum paste; metal oxides such as titanium oxide; metal sulfates such as barium sulfate. These heat ray radiation suppressors may be used alone or in combination of two or more. Among these heat ray radiation inhibitors, carbon materials and metal pastes are preferable, carbon materials are more preferred, and graphite is particularly preferred from the viewpoint of the effect of suppressing heat ray radiation.

  When the heat ray radiation inhibitor is included, the content thereof is preferably 0.1 parts by weight or more and 10 parts by weight or less with respect to 100 parts by weight in total of the first and second styrene resins. Preferably they are 1 weight part or more and 8 weight part or less.

  In the present invention, a radical generator may be used in combination. With the radical generator, the flame retardancy of the styrene resin extruded foam can be improved.

  Examples of the radical generator include 2,3-dimethyl-2,3-diphenylbutane, 2,3-diethyl-2,3-diphenylbutane, 3,4-dimethyl-3,4-diphenylhexane, 3, Dialkyldiphenylalkanes such as 4-diethyl-3,4-diphenylhexane; diphenylalkylalkenes such as 2,4-diphenyl-4-methyl-1-pentene and 2,4-diphenyl-4-ethyl-1-pentene; poly Polydialkylbenzenes such as -1,4-diisopropylbenzene; peroxides such as dicumyl peroxide; and the like.

  Among these, those that are stable under the resin processing temperature conditions are preferable, specifically, dialkyldiphenylalkanes and polydialkylbenzenes are preferable, 2,3-dimethyl-2,3-diphenylbutane, poly-1,4-diisopropylbenzene. Is more preferable.

  The radical generator is preferably 0.05 parts by weight or more and 0.5 parts by weight or less with respect to a total of 100 parts by weight of the first and second styrenic resins.

  In the present invention, for the purpose of improving the flame retardancy, a phosphorus flame retardant such as phosphate ester and phosphine oxide can be used in combination as long as the thermal stability performance is not impaired.

  Examples of the phosphate ester include triphenyl phosphate, tricresyl phosphate, trixylylenyl phosphate, cresyl diphenyl phosphate, 2-ethylhexyl diphenyl phosphate, trimethyl phosphate, triethyl phosphate, tributyl phosphate, tris (2-ethylhexyl). ) Phosphate, tris (butoxyethyl) phosphate, condensed phosphate ester, halogen-containing phosphate ester such as tris (tribromoneopentyl) phosphate, etc., especially triphenyl phosphate and tris (tribromoneopentyl) Phosphate is preferred. As the phosphine oxide, triphenylphosphine oxide is preferable. These phosphate esters and phosphine oxides may be used alone or in combination of two or more.

  When a phosphorus flame retardant flame retardant is included, the content is preferably 0.1 parts by weight or more and 2 parts by weight or less with respect to 100 parts by weight of the first and second styrene resins.

  Moreover, when manufacturing the styrene resin extrusion foam of this invention, the stabilizer for extrusion foaming can also be used as a 2nd stabilizer separately from the stabilizer used for the flame retardant composition. As the stabilizer for extrusion foaming (second stabilizer), the same stabilizer as that for the flame retardant composition can be used, among which epoxy compounds, phenol stabilizers, phosphite stabilizers, A monohydric alcohol partial ester is preferable, and a phenol-based stabilizer and a polyhydric alcohol partial ester are more preferable.

  When the extrusion foaming stabilizer (second stabilizer) is used, the amount thereof is 0.05 parts by weight or more and 10 parts by weight or less with respect to 100 parts by weight of the first and second styrenic resins. Is preferably 0.1 parts by weight or more and 5 parts by weight or less. The total amount of the stabilizer in the flame retardant composition and the stabilizer for extrusion foaming (second stabilizer) is 0.1 parts by mass or more with respect to 100 parts by weight of the first and second styrenic resins. 20 parts by mass or less, preferably 0.2 parts by weight or more and 10 parts by weight or less. Furthermore, the amount of the stabilizer for extrusion foaming (second stabilizer) is preferably 5 parts by weight or more and 200 parts by weight or less with respect to 100 parts by weight of the stabilizer in the flame retardant composition, and more preferably. Is 10 to 100 parts by weight, more preferably 20 to 50 parts by weight.

  In the styrene resin extruded foam of the present invention, processing aids; flame retardants other than the above; flame retardant aids; antioxidants; antistatic agents; Other additives such as an agent; a colorant such as a pigment; and the like may be used. Examples of the processing aid include fatty acid metal salts such as calcium stearate; fatty acid amides; fatty acid esters; liquid paraffin; olefin waxes; clay minerals such as talc and bentonite;

  The styrene resin extruded foam of the present invention is prepared by mixing a flame retardant composition and a second styrene resin and, if necessary, other additives and the like by a known mixing means such as dry blending. After being prepared, it is supplied to a heating and melting means such as an extruder, heated and melted and kneaded, a foaming agent is added to the premixed mixture to form a fluid gel-like mixture, and cooled to a temperature suitable for extrusion foaming. The mixture can be preferably produced by extruding and foaming the mixture into a low pressure region through a die.

  The heating temperature when heating and kneading the preliminary mixture may be higher than the temperature at which the styrenic resin used melts, but it is a temperature at which molecular degradation of the resin is suppressed as much as possible, including the influence of flame retardants. It is preferable to be, for example, 160 ° C. or higher and 240 ° C. or lower, more preferably 225 ° C. or lower. The melt kneading time can be adjusted according to the amount of extrusion per unit time, melt kneading means, and the like. As the melt-kneading means, for example, a screw-type extruder is preferable, and a screw-type single-screw extruder is more preferable, but there is no particular limitation as long as it is used for normal extrusion foaming.

  The addition of the foaming agent can be carried out at an arbitrary timing, but it is preferably carried out at a stage where the premix is sufficiently melt-kneaded. When adding the foaming agent, it is preferable to press-fit the foaming agent under a high pressure condition of, for example, 5 MPa or more, preferably 10 MPa or more. The pressure for press-fitting the foaming agent is adjusted according to the heating temperature and the foaming agent. The heating temperature of the premix when adding the foaming agent is preferably 160 ° C. or higher and 240 ° C. or lower, more preferably 180 ° C. or higher and 230 ° C. or lower.

  100-150 degreeC is preferable and the temperature at the time of extrusion foaming has more preferable 110-140 degreeC. Further, the pressure in the low pressure region for extruding and foaming the mixture is preferably 0.5 MPa or less, and more preferably atmospheric pressure (1013 hPa). For extrusion foaming, for example, a slit die having an opening having a linear slit shape can be preferably used. The thickness of the die is, for example, 0.5 to 100 mm, and the width is, for example, 10 to 1000 mm.

  The method of molding the foam that has been extruded and foamed is not particularly limited. For example, using a molding die and a molding roll in which a foam obtained by releasing pressure from a slit die is placed in close contact with or in contact with the slit die. A general method such as molding a plate-like foam having a large cross-sectional area can be used.

  The thickness of the styrene resin extruded foam of the present invention is not particularly limited and is appropriately selected depending on the application. For example, in the case of a heat insulating material used for applications such as building materials, in order to give preferable heat insulating properties, bending strength and compressive strength, those having a thickness like a normal plate-like material are preferable, usually 10 to 10 150 mm, preferably 20-100 mm.

  From the viewpoint of heat insulation, the average cell diameter (bubble diameter) in the styrene resin extruded foam of the present invention is preferably 0.02 mm or more and 1.5 mm or less, and 0.05 mm or more and 1.0 mm or less. More preferably.

  In the present invention, by using water as the other foaming agent, small bubbles (hereinafter referred to as small bubbles) having a cell diameter (cell diameter) of 0.2 mm or less in the styrene resin extruded foam, A foam having a cell structure in which large cells (hereinafter referred to as large cells) having a (cell diameter) of 0.25 mm or more (preferably 0.25 mm or more and 1 mm or less) are mixed in a sea-island shape is obtained. In the body, the heat insulation performance is further improved.

  In a foam structure with a mixture of small bubbles and large bubbles, the ratio of the area of small bubbles to the cross-sectional area of the foam (occupied area ratio per unit cross-sectional area of small bubbles) The rate is preferably 5% or more and 95% or less, more preferably 10% or more and 90% or less, further preferably 20% or more and 80% or less, and more preferably 25% or more. 70% or less is particularly preferable.

The density of the styrene resin extruded foam of the present invention is preferably 15 kg / m ³ or more and 50 kg / m ³ or less in order to give light weight and excellent heat insulating properties, bending strength, and compressive strength, More preferably, it is m ³ or more and 40 kg / m ³ or less. The styrene resin extruded foam preferably has a bending strength of 20 to 100 N / cm ² and a compressive strength of 5 to 70 N / cm ² .

  From the viewpoint of flame retardancy, the styrene resin extruded foam of the present invention preferably passes the combustion test method of JIS A9511.

  The oxygen index of the styrene resin extruded foam of the present invention is preferably 26% or more, for example, from the viewpoint of flame retardancy, more preferably 27% or more, and particularly preferably 28% or more. The upper limit of the oxygen index is not particularly limited, but for example, it is evaluated that the flame index is sufficiently excellent even at about 35% or less, particularly about 30% or less.

  The styrene resin extruded foam of the present invention has excellent thermal stability, flame retardancy and heat insulation, and is suitably used as a heat insulating material for building materials.

  EXAMPLES Hereinafter, the present invention will be described more specifically with reference to examples. However, the present invention is not limited by the following examples, but may be appropriately modified within a range that can meet the purpose described above and below. Of course, it is possible to implement them, and they are all included in the technical scope of the present invention. In the following, “parts” means “parts by weight” and “%” means “% by weight” unless otherwise specified.

The raw materials used in the examples and comparative examples are as follows.
(A) Styrenic resin / 680 (manufactured by PS Japan)
・ G9401 (manufactured by PS Japan)
(B) Flame retardant / brominated styrene-butadiene block polymer [available from Chemtura, EMERALD INNOVATION 3000, Mw 100,000 to 160,000, bromine content 65%]
(C) Stabilizer Epoxy compound / cresol novolak type epoxy resin [manufactured by Huntsman Japan, ECN-1280, epoxy equivalent 212-233 g / eq. ]
Phenol stabilizer / pentaerythritol tetrakis [3- (3 ′, 5′-di-tert-butyl-4′-hydroxyphenyl) propionate] [ANOX20 manufactured by Chemtura]
Phosphite stabilizer, 3,9-bis (2,4-di-tert-butylphenoxy) -2,4,8,10-tetraoxa-3,9-diphosphaspiro [5.5] undecane [Ultrax626 made by Chemtura]
Polyhydric alcohol partial ester / dipentaerythritol-adipic acid reaction mixture [Ajinomoto Finetechno, Pleniser ST210]
(D) Radical generator poly-1,4-diisopropylbenzene [CCPIB manufactured by UNITED INITIATORS]
(E) Foaming agent, isobutane [Mitsui Chemicals, Inc.]
・ Industrial butane [Made by Iwatani Corporation]
・ Water [tap water]
・ Dimethyl ether [Mitsui Chemicals, Inc.]
(F) Other additives, talc [manufactured by Hayashi Kasei, Talcan powder PK-Z]
Bentonite [Hojoen, Wenger Bright 11K]
・ Silica [Evonik Degussa Japan, Carplex BS304F]
·Calcium stearate

The evaluation methods implemented in the examples and comparative examples are as follows.
(1) Bromine Content in Flame Retardant Composition After decomposing a flame retardant composition containing a brominated flame retardant by an oxygen flask combustion method, the Br content was quantified by an ion chromatography method.

(2) 5% weight reduction temperature of flame retardant composition Sample weight: 7 mg
Measuring device: TG-DTG60A (manufactured by Shimadzu Corporation)
Measurement cell: Aluminum Measurement atmosphere: Nitrogen (20 ml / min)
Temperature condition: heated from room temperature (about 25 ° C.) to 400 ° C. at a rate of temperature increase of 10 ° C./min 5% weight reduction temperature: sample weight at 150 ° C. of the sample is used as a reference, and the sample weight is reduced by 5% Temperature to do.

(3) Appearance of the flame retardant composition (discoloration)
The appearance of the pelletized flame retardant composition was visually observed and evaluated according to the following criteria based on the degree of discoloration such as black stripes and black spots.
◎: No discoloration ○: No discoloration ×: Discoloration observed

(4) Appearance of flame retardant composition (pellet shape)
The cut surface by the strand cut method at the time of pelletizing the flame retardant composition was observed, and the one cut into a columnar shape was regarded as acceptable (◯), and the other one was regarded as unacceptable (x).

(5) Flammability of Extruded Foam Extruded foam samples obtained in Examples or Comparative Examples were stored indoors, and the flammability of the foam samples that had passed 7 days after production was measured according to JIS A9511. .
○: Satisfies the criteria that the flame disappears within 3 seconds, there is no residue, and the combustion limit indicator line is not exceeded.
X: The above criteria are not satisfied.

(6) Oxygen Index of Extruded Foam The oxygen index of the extruded foam obtained in Examples or Comparative Examples was measured according to JIS K 7201: 1999.

(7) Appearance of extruded foam (foreign matter generation / discoloration)
The appearance of the extruded foam was visually observed, and the case in which neither generation of foreign matter nor discoloration was observed was accepted (◯), and the case in which occurrence or discoloration of foreign matter was observed was rejected (x).

Example 1
[Production of flame retardant composition]
Brominated SBS block polymer (EMERALD INNOVATION 3000) as a flame retardant and styrene resin (polystyrene 680), cresol novolac type epoxy resin (ARALDITE ECN-1280), which is an epoxy compound as a stabilizer, phenol-based stable Pentaerythritol tetrakis [3- (3 ′, 5′-di-tert-butyl-4′-hydroxyphenyl) propionate] (ANOX20) as an agent, and 3,9-bis (2, which is a phosphite stabilizer) 4-Di-tert-butylphenoxy) -2,4,8,10-tetraoxa-3,9-diphosphaspiro [5.5] undecane (Ultranox 626) was weighed out and dry blended in the proportions shown in Table 1. This dry blended product is supplied to the same direction twin screw extruder of the caliber and L / D shown in Table 1, and extruded at the cylinder set temperature, screw rotation speed and discharge amount shown in Table 1, and the extrudate is produced by the strand cut method. It cut | disconnected and produced the pellet-form flame retardant composition. The resin temperature at the die outlet of the extruder was 195 ° C., and the specific energy of the extruder was as shown in Table 1. The 5% weight reduction temperature and appearance (discoloration / pellet shape) of the obtained flame retardant composition (pellet) were as shown in Table 1, and there were no problems.

[Production of extruded foam]
100 parts of a styrene resin (including the styrene resin in the flame retardant composition), 6.0 parts of the flame retardant composition (pellet) obtained above, poly-1,4-diisopropylbenzene as a radical generator A premix was prepared by dry blending 0.1 part, 0.1 part calcium stearate, 0.5 part talc, 0.5 part bentonite and 0.2 part silica.
Supply the above premixed mixture at about 800 kg / hr to a single screw extruder (first extruder) with a diameter of 150 mm, a single screw extruder (second extruder) with a diameter of 200 mm, and an extruder connected in series with a cooler. did.
The premix supplied to the first extruder was melted or plasticized and kneaded by heating to a resin temperature of 225 ° C. A foaming agent (0.7 parts of water (tap water), 3.5 parts of isobutane and 2 parts of dimethyl ether with respect to 100 parts of styrene resin) was press-fitted into the kneaded material near the tip of the first extruder. Thereafter, the kneaded product is sent out to a second extruder and a cooler connected to the first extruder, the resin temperature is cooled to 120 ° C. with this cooler, and a rectangle with a thickness of 2 mm and a width of 400 mm provided at the tip of the cooler. After extrusion foaming from the cross-sectional die into the atmosphere, an extruded foam plate having a cross-sectional shape of 60 mm thickness x 1000 mm width is obtained by a molding die placed in close contact with the die and a molding roll placed downstream thereof. And cut with a cutter into a thickness of 50 mm × width of 910 mm × length of 1820 mm. As shown in Table 1, all of the obtained foams had no problem with the combustibility, oxygen index, and appearance (foreign matter generation / discoloration).

(Example 2)
A flame retardant composition was obtained by the same operation as in Example 1 except that the barrel temperature was changed to the temperature shown in Table 1. At this time, the resin temperature at the die outlet was 197 ° C. As shown in Table 1, the obtained flame retardant composition had no problem in any of 5% weight loss temperature, appearance (discoloration), and appearance (pellet shape). Further, an extruded foam was obtained by the same operation as in Example 1 except that the obtained flame retardant composition was used. As shown in Table 1, the obtained foam was satisfactory in terms of flammability, oxygen index, and appearance (foreign matter generation / discoloration).

(Example 3)
A flame retardant composition was obtained in the same manner as in Example 1 except that the screw rotation number was changed to the value shown in Table 1. At this time, the resin temperature at the die outlet was 198 ° C. As shown in Table 1, the obtained flame retardant composition had no problem in any of 5% weight loss temperature, appearance (discoloration), and appearance (pellet shape). Further, an extruded foam was obtained by the same operation as in Example 1 except that the obtained flame retardant composition was used. As shown in Table 1, the obtained foam was satisfactory in terms of flammability, oxygen index, and appearance (foreign matter generation / discoloration).

Example 4
A flame retardant composition was obtained by the same operation as in Example 3 except that the discharge amount was the amount shown in Table 1. At this time, the resin temperature at the die outlet was 197 ° C. The obtained flame retardant composition had no problem in any of the 5% weight loss temperature, appearance (discoloration), and appearance (pellet shape). Further, an extruded foam was obtained by the same operation as in Example 1 except that the obtained flame retardant composition was used. As shown in Table 1, the obtained foam was satisfactory in terms of flammability, oxygen index, and appearance (foreign matter generation / discoloration).

(Example 5)
A flame retardant composition was obtained in the same manner as in Example 1 except that the diameter, L / D, screw rotation speed, and discharge amount were set to the values shown in Table 1. At this time, the resin temperature at the die outlet was 192 ° C. The obtained flame retardant composition had no problem in any of the 5% weight loss temperature, appearance (discoloration), and appearance (pellet shape). Further, an extruded foam was obtained by the same operation as in Example 1 except that the obtained flame retardant composition was used. As shown in Table 1, the obtained foam was satisfactory in terms of flammability, oxygen index, and appearance (foreign matter generation / discoloration).

(Example 6)
A flame retardant composition was obtained in the same manner as in Example 5 except that the screw rotation speed and the discharge amount were set to the values shown in Table 1. At this time, the resin temperature at the die outlet was 211 ° C. The obtained flame retardant composition had no problem in any of the 5% weight loss temperature, appearance (discoloration), and appearance (pellet shape). Extruded foam was obtained by the same operation as in Example 1 except that the obtained flame retardant composition was used. As shown in Table 1, the obtained foam was satisfactory in terms of flammability, oxygen index, and appearance (foreign matter generation / discoloration).

(Example 7)
A flame retardant composition was obtained in the same manner as in Example 1 except that the diameter, L / D, screw rotation speed, and discharge amount were set to the values shown in Table 1. At this time, the resin temperature at the die outlet was 186 ° C. As shown in Table 1, the obtained flame retardant composition had no problem in any of 5% weight loss temperature, appearance (discoloration), and appearance (pellet shape). Further, an extruded foam was obtained by the same operation as in Example 1 except that the obtained flame retardant composition was used. As shown in Table 1, the obtained foam was satisfactory in terms of flammability, oxygen index, and appearance (foreign matter generation / discoloration).

(Example 8)
A flame retardant composition was obtained in the same manner as in Example 1 except that the styrene resin was G9401 made by PSJ. At this time, the resin temperature at the die outlet was 205 ° C. As shown in Table 1, the obtained flame retardant composition had no problem in any of 5% weight loss temperature, appearance (discoloration), and appearance (pellet shape). Further, an extruded foam was obtained by the same operation as in Example 1 except that the obtained flame retardant composition was used. As shown in Table 1, the obtained foam was satisfactory in terms of flammability, oxygen index, and appearance (foreign matter generation / discoloration).

Example 9
Pentaerythritol tetrakis [3- (3 ′, 5′-di-tert-butyl-4′-hydroxyphenyl) propionate] (ANOX20), a phenolic stabilizer, dipentaerythritol-adipic acid reaction as a polyhydric alcohol partial ester A flame retardant composition was obtained by the same operation as in Example 1 except that the amount of the mixture (Plenizer ST210) was changed to the amount shown in Table 1. At this time, the resin temperature at the die outlet was 198 ° C. As shown in Table 1, the obtained flame retardant composition had no problem in any of 5% weight loss temperature, appearance (discoloration), and appearance (pellet shape). Further, an extruded foam was obtained by the same operation as in Example 1 except that the obtained flame retardant composition was used. As shown in Table 1, the obtained foam was satisfactory in terms of flammability, oxygen index, and appearance (foreign matter generation / discoloration).

(Comparative Example 1)
A flame retardant composition was obtained in the same manner as in Example 1 except that the barrel temperature was changed to the temperature shown in Table 1. As shown in Table 1, the obtained flame retardant composition is inferior to the Examples in terms of 5% weight loss temperature, appearance (discoloration such as black streaks) and appearance (pellet shape). It was a thing. Further, an extruded foam was obtained by the same operation as in Example 1 except that the obtained flame retardant composition was used. As shown in Table 1, the obtained foam was inferior in combustibility, oxygen index, and appearance (foreign matter generation / discoloration) as compared with the Examples.

(Comparative Example 2)
A flame retardant composition was obtained by the same operation as in Example 4 except that the discharge amount was changed to the amount shown in Table 1. As shown in Table 1, the obtained flame retardant composition has a 5% weight reduction temperature of 246 ° C., appearance (discoloration such as black streaks), and appearance (pellet shape) compared to the examples. It was inferior. Further, an extruded foam was obtained by the same operation as in Example 1 except that the obtained flame retardant composition was used. As shown in Table 1, the obtained foam was inferior in combustibility, oxygen index, and appearance (foreign matter generation / discoloration) as compared with the Examples.

(Comparative Example 3)
A flame retardant composition was obtained by the same operation as in Example 1 except that L / D was a value shown in Table 1. As shown in Table 1, the obtained flame retardant composition has no problem in appearance (pellet shape), but compared with the examples in terms of 5% weight reduction temperature and appearance (discoloration such as black streaks occur). It was inferior. Further, an extruded foam was obtained by the same operation as in Example 1 except that the obtained flame retardant composition was used. As shown in Table 1, the obtained foam was inferior in combustibility, oxygen index, and appearance (foreign matter generation / discoloration) as compared with the Examples.

Claims (7)

Obtained by kneading the first styrenic resin, the brominated styrene-butadiene block polymer, and the stabilizer under the conditions of an extruder barrel temperature of 180 ° C. or less and a specific energy of 0.50 kWh / kg or less, and ,
A flame retardant composition having a 5% weight loss temperature of from 255 ° C to 270 ° C by thermogravimetric analysis.   The flame retardant composition according to claim 1, which is obtained by kneading in an extruder having a ratio (L / D) of an effective length L of the screw to an outer diameter D of 52 or less.   The flame retardant composition according to claim 1 or 2, which is obtained by kneading with an extruder having a discharge amount (Q / N) per rotation of the screw of 0.6 kg / Hr / rpm or more.   The first styrene resin is contained in an amount of 20 parts by weight or more and 200 parts by weight or less and a stabilizer is contained in an amount of 5 parts by weight or more and 75 parts by weight or less based on 100 parts by weight of the brominated styrene-butadiene block polymer. The flame retardant composition according to any one of?   The flame retardant composition according to any one of claims 1 to 4, wherein the stabilizer is at least one selected from the group consisting of an epoxy compound, a phenol-based stabilizer, a phosphite-based stabilizer, and a polyhydric alcohol partial ester. object.   A styrene resin extruded foam obtained by extrusion foaming a mixture containing the flame retardant composition according to any one of claims 1 to 5, a second styrene resin, and a foaming agent.   The styrene resin extruded foam according to claim 6, wherein the mixture further contains a second stabilizer.