• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
  • 同族专利
  • 引用文献
  • 法律状态
  • 优先权
    • 专利摘要:
    A non-halogen flame-retardant polyester resin composition having a high flame retardancy and a small amount of flame retardant and no dropping during combustion, excellent mechanical strength and resin kneading, and no bleed-out by annealing It consists of 100 weight part of polyesters, such as polytetramethylene terephthalate, 1-15 weight part of coating red powders, and 3-70 weight part of novolak-type phenol resins.
    公开号:KR20000064569A
    申请号:KR1019980707077
    申请日:1998-01-06
    公开日:2000-11-06
    发明作者:미오꼬 스즈끼；노리쓰구 사이끼
    申请人:야스이 쇼사꾸；데이진 가부시키가이샤；
    IPC主号:
    专利说明:

    Flame Retardant Resin Composition
    Polyester resins, including polybutylene terephthalate, have excellent mechanical properties, heat resistance, chemical resistance, and the like, and thus are widely used as molded articles for applications in the fields of electric and electronics and automobiles.
    Among these, many applications are required for flame retardancy, and resins having flame retardance are mainly used by using halogen compounds and antimony compounds as flame retardants and flame retardant aids.
    However, halogen-based flame retardants may corrode metals whose decomposition products are electrical products, and some halogen-based flame retardants have a problem of environmental impact, and non-halogen flame-retardant resins are required.
    Phosphorus compounds are present as non-halogen flame retardants, and low molecular weight phosphate esters such as triphenylphosphate (TPP) have been frequently used as a typical organic phosphorus compound. However, polyester resins such as polybutylene terephthalate have a relatively high processing temperature, and in the case of low molecular weight phosphate esters, there is a problem of bleed-out and heat resistance.
    Japanese Patent Laid-Open No. 7-126498 discloses a polyester resin, an epoxy compound having two or more epoxy groups in a molecule, and a phosphorus, nitrogen, and boron compound having a functional group capable of reacting with a phenol resin and / or an epoxy group. Disclosed is a non-halogen flame retardant for a polyester resin, which is obtained by melting a selected one or more non-halogen flame retardant compounds.
    Japanese Patent Laid-Open No. 7-278267 discloses a flame-retardant polyester resin composition in which 5 to 50 parts by weight of the non-halogen-based flame retardant is blended into 100 parts by weight of a polyester resin.
    The non-halogen flame retardant is characteristic in that an epoxy compound having two or more epoxy groups in a molecule is used.
    Japanese Patent Application Laid-Open No. 8-188717 discloses thermoplastic resins such as polystyrene and polyester, phosphorus compounds such as phosphate esters and phosphite esters, phenols (for example cresol) and aralkyl halides (for example, α, α-dichloro A flame retardant resin composition composed of a phenol aralkyl resin such as a reaction product of -p-xylene) is disclosed.
    Japanese Patent Application Laid-Open No. 8-208884 discloses a flame retardant resin composition comprising a thermoplastic resin such as polystyrene or polyester, a phosphorus compound such as phosphate ester or phosphite ester, and a phenol resin from phenols substituted with ortho or para positions. It is.
    On the other hand, in Journal of Fire Retardant Chemistry vol. 7, 69-76, 1980, it is disclosed that polystyrene is flame retarded by red phosphorus and phenol resin.
    Japanese Laid-Open Patent Publication No. 2-37370 discloses 99 to 34 parts by weight of thermoplastic polyester resin having a softening point of 150 ° C. or higher, such as polyethylene terephthalate, 1 to 25 parts by weight of red phosphorus coated with a thermosetting resin, and a reinforcing filler. Disclosed are a flame retardant polyester resin composition composed of 10 to 55 parts by weight.
    The present invention relates to a flame retardant resin composition, and more particularly, has a high flame retardancy, and no dropping (drip) of the molten resin occurs during combustion, so that mechanical strength and resin kneading processability are good, and annealing The present invention relates to a non-halogen flame retardant resin composition in which bleed out does not occur on the surface of a molded article.
    For this reason, the objective of this invention is providing the flame-retardant resin composition which consists of a novel composition.
    Another object of the present invention is to provide a flame retardant resin composition which gives a molded article having a high flame retardancy with a smaller flame retardant amount of a non-halogen flame retardant and does not cause dropping (drip) of molten resin when it is burned. Is in.
    Still another object of the present invention is to provide a flame retardant polyester resin composition having good mechanical strength and resin kneading processability, and which does not cause bleed-out on the surface of a molded article by annealing.
    Still other objects and advantages of the present invention will become apparent from the following description.
    According to the present invention, the above objects and advantages of the present invention,
    (A) 100 parts by weight of a thermoplastic aromatic polyester resin,
    (B) 3 to 70 parts by weight of a novolac phenol resin, and
    (C) 1 to 15 parts by weight of the coated red powder having a film of cured resin
    It is achieved by the flame-retardant resin composition which consists of.
    In the present invention, the thermoplastic aromatic polyester resin (A) is a polyester having an aromatic dicarboxylic acid as a main dicarboxylic acid component and an aliphatic diol having 2 to 10 carbon atoms as a main glycol component. Preferably at least 80 mol%, more preferably at least 90 mol% of the dicarboxylic acid component consists of the aromatic dicarboxylic acid component. The glycol component is preferably 80 mol% or more, and more preferably 90 mol% or more of the glycol component is composed of aliphatic diols having 2 to 10 carbon atoms.
    As aromatic dicarboxylic acid, terephthalic acid, isophthalic acid, phthalic acid, methyl terephthalic acid, methyl isophthalic acid, 2, 6- naphthalenedicarboxylic acid, etc. are preferable, for example. These can be used together by 1 type or 2 types of paper. As main dicarboxylic acid other than aromatic dicarboxylic acid, For example, aliphatic or alicyclic, such as adipic acid, sebacic acid, decane dicarboxylic acid, azelaic acid, dodecanedicarboxylic acid, cyclohexanedicarboxylic acid, etc. Group dicarboxylic acid etc. are mentioned.
    Examples of the aliphatic diol having 2 to 10 carbon atoms include aliphatic diols such as ethylene glycol, trimethylene glycol, tetramethylene glycol, hexamethylene glycol and neopentyl glycol, and alicyclic diols such as 1,4-cyclohexanedimethanol. Can be. These aliphatic diols can be used together by 1 type or 2 types. As main glycol other than C2-C10 aliphatic diol, p, p'- dihydroxyethoxy bisphenol A, polyoxyethylene glycol, etc. are mentioned, for example.
    As the thermoplastic aromatic polyester resin (A), among them, the main dicarboxylic acid component is at least one dicarboxylic acid selected from the group consisting of terephthalic acid and 2,6-naphthalenedicarboxylic acid, and the main diol component is ethylene. Preference is given to polyesters or polyester elastomers comprising ester units which are at least one diol selected from the group consisting of glycols and tetramethylene glycol.
    Of these, polyester elastomers having tetramethylene terephthalate or tetramethylene-2,6-naphthalenedicarboxylate as main repeating units of polyester or hard segment as main repeating units are more preferred.
    As a soft component of the polyester elastomer in which tetramethylene terephthalate or tetramethylene-2,6-naphthalenedicarboxylate is the main repeating unit of the hard segment, for example, dicarboxylic acid is terephthalic acid, isophthalic acid, sebacic acid and adipic acid. composed of the group of one or more dicarboxylic acids is selected from the consisting of is, the diol component selected from the group consisting of long-chain diol, and H (OCH 2 CH 2) i OH (i = 2 ~ 5) having a carbon number of 5-10 It is preferable that it consists of at least 1 type of diol, and also consists of polyester whose melting | fusing point is 100 degrees C or less or amorphous, or consists of polycaprolactone.
    As for the intrinsic viscosity measured in 35 degreeC and orthochlorophenol of the thermoplastic aromatic polyester resin in this invention, 0.5-1.4 are preferable, More preferably, it is 0.6-1.2. If the intrinsic viscosity is less than 0.5, the mechanical strength of the resulting composition is lowered, which is not preferable.
    The novolak-type phenol resin used in the present invention is obtained by polycondensing phenol and formaldehyde in the presence of an acid catalyst. 600-13,000 are preferable and, as for the weight average molecular weight, 650-7,000 are more preferable.
    The addition amount of a novolak-type phenol resin is 3-70 weight part with respect to 100 weight part of thermoplastic aromatic polyester resins (A). If the added amount is less than 3 parts by weight, the flame retardancy is not sufficient, and if it exceeds 70 parts by weight, the mechanical properties of the molded article are lowered. Preferable addition amount is 5-50 weight part.
    In the present invention, red phosphorus is used as a coated red phosphorus powder having a film of cured resin. Red phosphorus alone may cause ignition or phosphine generation due to high temperature, mechanical shock, or the like.
    The cured resin of the coating of the coated red powder preferably consists of a cured product of at least one curable resin selected from the group consisting of phenol resins, epoxy resins, unsaturated polyester resins, melamine resins, urea resins and aniline resins.
    The coated red powder may further contain an inorganic compound selected from the group consisting of aluminum hydroxide, magnesium hydroxide, zinc hydroxide and titanium hydroxide in the cured resin of the film, and further, aluminum hydroxide, magnesium hydroxide, zinc hydroxide. And a coating of an inorganic compound selected from the group consisting of hydroxides of titanium in contact with red phosphorus under the coating of the cured resin.
    The average particle diameter of the coated red powder having the film of the cured resin is preferably in the range of 5 to 40 µm, and more preferably in the range of 25 to 35 µm.
    The coating red powder (C) is mix | blended so that it may become a range of 1-15 weight part with respect to 100 weight part of aromatic polyester resins (A). If it is less than 1 weight part, flame retardance is inadequate, and if it exceeds 15 weight part, the mechanical property of the molded article obtained from a flame-retardant resin composition will fall, and it is unpreferable.
    The coated red powder is remarkably improved in terms of safety such as handling compared to the red phosphorus alone, but in order to provide further stability in use, it is preferable to use a master pellet that has been previously melt-kneaded with a thermoplastic resin. Moreover, by using a master pellet, the resin composition excellent in the mechanical strength of the molded article obtained can be provided.
    The thermoplastic resin in this case is not particularly limited, and polyethylene, polypropylene, EPDM, ethylene ethyl acrylate, ethylene methyl acrylate, polyester, polyamide, polycarbonate and the like can be given. Usually, the thermoplastic aromatic polyester resin used as (A) component is preferable.
    As for content of the coating red powder (C) in a master pellet, 15 to 35 weight% is preferable. If the amount is less than 15% by weight, the amount of the added master pellets is relatively increased. If the amount is more than 35% by weight, the master pelletization is difficult and there is a risk of deterioration of stability.
    The master pellet thus obtained is added in an amount of 5 to 70 parts by weight based on 100 parts by weight of the aromatic polyester resin (A). It is because the preferable flame retardance cannot be obtained when it is less than 5 weight part, and when it exceeds 70 weight part, the original characteristic of a polyester resin will be impaired.
    The flame-retardant resin composition of this invention can contain an inorganic filler further in the range which does not impair the objective of this invention.
    Examples of such inorganic fillers include granular or amorphous fillers such as calcium carbonate, titanium oxide, feldspar minerals, clay, white carbon, carbon black, glass bis and the like; Plate-like fillers such as kaolin clay, tark and the like; Fillers in the shape of scales such as glass flakes, mica and graphite; And fibrous fillers such as glass fibers, ullastite and potassium titanate.
    It is preferable to contain an inorganic filler in the range of 5-150 weight part with respect to 100 weight part of aromatic polyester resins (A).
    Moreover, the flame retardant resin composition of this invention can contain a fluororesin. Examples of the fluororesin include polyterafluoroethylene and tetrafluoroethylene / ethylene copolymers. The preferable addition amount of a fluororesin is 0.01-10 weight part with respect to 100 weight part of aromatic polyester resins (A). When it exceeds 10 parts by weight, it is not preferable in view of moldability. By adding a fluororesin, the combustion time of a resin molding can be shortened.
    Moreover, the flame-retardant resin composition of this invention can contain a silicon powder. The silicon powder has a structure in which silane and silicon are supported on silica. The addition amount of a silicon powder is 0.01-10 weight part with respect to 100 weight part of aromatic polyester resins (A). When the addition amount exceeds 10 parts by weight, it is not preferable in view of moldability.
    In addition, the flame-retardant resin composition of the present invention may further contain additives commonly used, such as antioxidants, heat stabilizers, ultraviolet absorbers, lubricants, nucleating agents, plasticizers, mold release agents, pigments, and impact modifiers such as various elastomers.
    As a manufacturing method of the flame-retardant resin composition of this invention, the method of simultaneously melt-kneading each component, such as a polyester resin, a coating red phosphorus powder or a red phosphorus master pellet, a novolak-type phenol resin, glass fiber, using an extruder simultaneously. In addition, any one may be melt kneaded in advance.
    The resin composition obtained by melt-kneading with an extruder is molded after being cut into pellets by a pelletizer, but the method may be any molding method such as injection molding or blow molding.
    The flame-retardant resin composition of this invention is used suitably for injection molded articles, such as electronic and electrical components, such as a home appliance and OA apparatus. Specifically, it can be used for switch parts, motor parts, ignition coil cases, coil bobbins, connectors, relay cases, fuse cases, and the like.
    Hereinafter, the present invention will be described in more detail with reference to Examples. In addition, "part" shows a "weight part" in an Example. Intrinsic viscosity was measured at 35 ° C. using an orthochlorophenol solvent. In addition, each test was evaluated in accordance with the following method.
    Flame retardance: By the test method of UL94V, flame retardance was evaluated using the test piece of thickness of 1/8 inch, 1/16, 1/32. The flame retardancy was classified into four types of V-0, V-1, V-2, and HB according to the evaluation method described in UL94. In addition to this determination method, dripping data was also described. For the effects of the fluororesin and the silicon powder, the average burn time per one was described.
    Oxygen index (O.I): based on JIS K7201
    Bending Strength: According to ASTM-D790
    Deformation Load Temperature: According to ASTM-D648-56.
    Bleed-out property: After performing an annealing process at 150 degreeC x 72 hours using the combustion test piece, it visually evaluated that the powder or liquid oozes out on the surface of a molded article by x, and the thing which does not seep out.
    Evaluation of kneading processability: The case where there was blocking under the hopper was evaluated by × and the absence of ○.
    Examples 1-11 and Comparative Examples 1-11
    The composition of Examples 1-11 is shown in Table 1, and the composition of Comparative Examples 1-11 is shown in Table 2. The red master pellets were prepared by melt kneading 30% by weight of phenolic resin and 70% by weight of polybutylene terephthalate resin. In both of the extruders, a twin screw extruder (TEX44, manufactured by Nippon Seiko Sho Co., Ltd.) was used, and the cylinder temperatures of Examples 1 to 9 and Comparative Examples 1 to 9 were 260 ° C, Example 10, and Comparative Examples. 10 melt-kneaded at 230 degreeC, Example 11, and Comparative Example 11 at 270 degreeC, discharge amount 40 kg / hr, and rotation speed 150rpm, and made into the chip form with the cutter. All of the extrusion processability in the examples were stable because almost no thread breaks occurred.
    After drying the obtained chip at 120 ° C for 5 hours, the melting temperature was 260 ° C for Examples 1-9 and Comparative Examples 1-9, 60 ° C for mold temperature, Example 10 and Comparative Example 10 for 230 ° C for melting temperature, and mold temperature. Was set at the conditions of 80 degreeC, Example 11, and the comparative example 11 at 270 degreeC, and mold temperature of 80 degreeC, and the combustion test piece, the tension test piece, and the bending test piece were created.
    Using these specimens, the combustion test (1/8, 1/16 inch for UL94V glass non-hardened system, 1/8, 1/16, 1/32 inch, and oxygen index for glass reinforced system), tensile test, bending The results of the test, the weighted strain temperature test, the bleed-out test by annealing, and the kneading workability results are shown in Tables 3, 4, and 5.
    In addition, the method for producing the surface-coated coated red phosphorus is suspended in red water, an aqueous solution of aluminum sulfate is added, the aqueous sodium hydroxide solution is added dropwise with sufficient stirring, heated at 50 ° C. for 30 minutes, and then phenol and formalin are added. What was obtained by heating to 80 degreeC, adding phosphoric acid under stirring, cooling and stirring at the same temperature for 1 hour, then cooling, filtration, washing with water and drying was used.
    The furtherance (part)Example 1Example 2Example 3Example 4Example 5Example 6Example 7Example 8Example 9Example 10Example 11 PBT100100100100100100100100100 PBT Elastomer 100PET 100 glass fiber 606060606060 60 Cloth Red Powder3 Red Master Pellets1320102020652020 1320 Phenolic Resin2020102040202020202020 Fluorine Resin One Silicone powder 2 PBT: Intrinsic viscosity of polytetramethylene terephthalate Teijin Co., Ltd. 1.07 PBT elastomer: Polyester polyester-based elastomer Teijin Co., Ltd. manufactured Nuberan Q4110AN Intrinsic viscosity 1.03 0.83 Glass fiber: T124 coated red powder manufactured by Asahi Glass Co., Ltd .: Red phosphorus coated with phenolic resin and aluminum hydroxide Nova Excel 140 Rinka Chemical Co., Ltd. Red phosphorus master pellet: Red phosphorus coated with phenolic resin and aluminum hydroxide Nova Excel 140 Rinka Chemical Co., Ltd., thermoplastic resin: Polybutylene terephthalate Teijin Co., Ltd. intrinsic viscosity 0.87 Phenolic resin: Novolac type phenolic resin Sumito Modurez Co., Ltd. PR-53195 Fluoro resin Polytetrafluoroethylene Daiseng Industrial Co., Ltd. FA100 silicone powder: Toray Downing Silicone Co., Ltd. DC4-7105
    The furtherance (part)Comparative Example 1Comparative Example 2Comparative Example 3Comparative Example 4Comparative Example 5Comparative Example 6Comparative Example 7Comparative Example 8Comparative Example 9Comparative Example 10Comparative Example 11 PBT100100100100100100100100100 PBT Elastomer 100PET 100 glass fiber 60606060 60 Red Master Pellets213 13132060 Phosphate Ester 2020202020 Phenolic Resin222020202020 Melamine cyanurate 20 Diallyl phthalate20 Epoxy compoundOne Phosphoric acid ester: Oya Chemical Co., Ltd. PX201 Iron oxide: Fe 3 O 4 Reagent 1st grade melamine cyanurate manufactured by Wako Pure Chemical Industries, Ltd .: MC490 diallyl phthalate manufactured by Nissan Kagaku Co., Ltd. Manufacture DAP-K Epoxy Compound: Yuca Shell Epoxy Co., Ltd. Epicoat 815
    characteristicExample 1Example 2Example 3Example 4Example 5Example 6Example 9Example 10Example 11 1/8 inch UL94 CombustibleV-0V-0V-0V-0V-0V-0V-0V-0V-0 Drip (drip)0/100/100/100/100/100/100/100/100/10 1/16 inch UL9 4V-0V-0V-0V-0V-0V-0V-0V-0V-0 Drip (drip)0/100/100/100/100/100/100/100/100/10 1/32 '' UL94 Combustible--V-0V-0V-0V-0V-0-V-0 Drip (drip)--0/100/100/100/100/10-0/10 Oxygen Index (%)323235383739383338 Bending Strength (MPa)105105205200211195101-215 Load Deflection Temperature (1.82MPa)707122021421120469-233 Annealed bleed out○○○○○○○○○ Blocking property during kneading○○○○○○○○○
    characteristicExample 4Example 7Example 8 1/8 inch UL94 CombustibleV-0V-0V-0 Average burning time (seconds)3.42.93.0 Drip (drip)0/100/100/10 1/16 '' UL94 CombustibleV-0V-0V-0 Average burning time (seconds)4.44.04.0 Drip (drip)0/100/100/10 1/32 '' UL94 CombustibleV-0V-0V-0 Average burning time (seconds)4.94.34.5 Drip (drip)0/100/100/10 Oxygen Index (%)383738
    characteristicComparative Example 1Comparative Example 2Comparative Example 3Comparative Example 4Comparative Example 5Comparative Example 6Comparative Example 7Comparative Example 8Comparative Example 9Comparative Example 10Comparative Example 11 1/8 inch UL94 CombustibleV-2HBV-0V-2HBHBHBV-0V-0V-0V-0 Drip (drip)10/107/100/1010/105/103/103/100/100/100/100/10 1/16 '' UL94 CombustibleHBV-2V-2V-2V-2HBV-2V-1V-2V-2V-1 Drip (drip)10/1010/105/1010/1010/1010/107/100/102/106/100/10 1/32 '' UL94 Combustible----V-2V-2V-2---- Drip (drip)----10/1010/1010/10---- Oxygen Resin (%)2324282122252532292733 Flexural Strength (MPa)8280849387203205129132-145 Load deflection temperature (1.82MPa)5860616463213212165132-181 Annealed Breeding Out○○×○×○○×××× Blocking property during kneading○○×○×○○××××
    In Example 1, 13 parts by weight of a master pellet (hereinafter referred to as red phosphorus master) moistened with 100 parts by weight of PBT resin and 20 parts by weight of an uncured phenol resin (hereinafter simply referred to as phenol resin) were mixed. Is a mixture of 20 parts by weight of the master and 20 parts by weight of the phenol resin, which were added to 100 parts by weight of the PBT resin, and all showed V-0 in the UL-94 combustion test, and exhibited excellent mechanical properties and no bleed-out.
    On the other hand, the comparative example 1 mix | blended 2 weight part of masters reddened with 2 weight part of phenol resins with 100 weight part of PBT resins, and since the compounding quantity of a red phosphorus master and a phenol resin was not suitable, sufficient flame retardance was not acquired. Comparative Example 2 was composed of 100 parts by weight of PBT resin, 13 parts by weight of red phosphorus master, and 2 parts by weight of phenol resin, and thus, sufficient flame retardancy could not be obtained because the amount of phenol resin was not appropriate.
    In Comparative Example 3, 20 parts by weight of phosphate ester and 20 parts by weight of phenol resin were used by converting the master into 100 parts by weight of PBT resin as a phosphorus flame retardant, but flame retardancy of V-0 was obtained at 1/8 inch. In inches, sufficient flame retardancy could not be obtained, and when phosphate ester was used, bleed-out at the time of annealing was severe, and white powder adhered to the molded article surface.
    In Comparative Example 4, 20 parts by weight of melamine cyanurate was mixed with 13 parts by weight of the master moistened with 100 parts by weight of PBT resin and phenol resin, but the problem of non-dropping was not solved when using melamine cyanurate. Inch, 1/16 inch could not obtain sufficient flame retardancy.
    In Comparative Example 5, 20 parts by weight of diallyl phthalate was mixed with 13 parts by weight of a master moistened with 100 parts by weight of PBT resin and a phenol resin, but did not have a flame retardant effect. Examples 1 and 2 and Comparative Examples 3 to 5 From the results, it was confirmed that a particularly high flame retardance can be obtained when a certain amount of red phosphorus master and phenol resin are used in combination.
    Example 3 mix | blended 60 weight part of glass fibers, 10 weight part of red phosphorus masters, and 10 weight part of phenol resins with respect to 100 weight part of PBT resins, and the flame retardance of V-0 was obtained to the thickness of 1/32 inch. Moreover, it had high mechanical characteristics, no bleed-out, and blocking was also effective.
    Similarly, Example 4 was blended with 100 parts by weight of PBT resin, 60 parts by weight of glass fiber, 20 parts by weight of red phosphorus master, and 20 parts by weight of phenol resin, and the same high flame retardancy and good bleed-out and blocking properties as in Example 3. Have Example 5 blended 100 parts by weight of PBT resin, 60 parts by weight of glass fiber, 20 parts by weight of red phosphorus master, and 40 parts by weight of phenolic resin to obtain high flame retardancy and good bleed-out and blocking properties as in Examples 3 and 4. lost.
    Example 6 mix | blended 60 weight part of glass fibers, 65 weight part of red masters, and 20 weight part of phenol resins by 100 weight part of PBT resin, and the same result as Example 3, 4, 5 was obtained.
    On the other hand, in Comparative Example 6, 60 parts by weight of glass fiber and 20 parts by weight of red master were blended with 100 parts by weight of PBT resin, and when phenol resin was not blended, only low flame retardancy was obtained. In Comparative Example 7, the red phosphorus master was increased to 60 parts by weight with respect to 100 parts by weight of PBT resin and 60 parts by weight of glass fiber, but the same flame retardancy as that of Comparative Example 6 was obtained. The thermosetting phenol resin used was not able to impart sufficient flame retardance to the PBT resin, and it was found that the flame retardant effect of V-0 was expressed only when the non-curable phenol resin was added during extrusion kneading.
    In Comparative Example 8, when 100 parts by weight of PBT resin and 60 parts by weight of glass fiber were used, 20 parts by weight of phosphate ester and 20 parts by weight of phenol resin were used instead of the reddish master, so that sufficient flame retardancy was not obtained and bleeds on the surface of the molded product after annealing. Out was shown, and blocking occurred at the top of the screw input hole during extrusion.
    In Comparative Example 9, 1 part by weight of the epoxy compound was further added to 20 parts by weight of the phosphate ester and 20 parts by weight of the phenol resin based on the composition of Comparative Example 8, 100 parts by weight of the PBT resin and 60 parts by weight of the glass fiber, but bleed-out was suppressed. I could not.
    Example 9 blended 60 parts by weight of glass fiber, 3 parts by weight of red phosphorus powder and 20 parts by weight of phenolic resin in 100 parts by weight of PBT resin, and the flame retardancy, bleed out property and blocking properties were all good, similar to the master pellets, In the state of, it becomes a target of dangerous goods, and there exists a possibility that a problem, such as flammability to an impact, may arise.
    Example 10 was blended with 13 parts by weight of the master soaked in 100 parts by weight of polyester elastomer and 20 parts by weight of phenol resin, and all of the flame retardancy, the bleed out property and the blocking property were good.
    On the other hand, in Comparative Example 10, 20 parts by weight of the phosphate ester and 20 parts by weight of the phenol resin were blended with 100 parts by weight of the polyester elastomer, but when the thickness became thin, the flame retardancy was insufficient, and the bleed out property and the blocking property were also poor.
    Example 11 was mixed with 100 parts by weight of PET resin, 20 parts by weight of the red pepper master and 60 parts by weight of phenol resin. On the other hand, in Comparative Example 11, 20 parts by weight of phosphate ester and 20 parts by weight of phenol resin were blended in 100 parts by weight of PET fiber and 60 parts by weight of glass fiber. In Example 11, high flame retardancy of V-0 to a thickness of 1/32 inch was obtained, and mechanical properties, bleed out property, and blocking property were also good. On the other hand, in Comparative Example 11, as the thickness became thin, the flame retardancy decreased, and the mechanical properties, the bleed out property, and the blocking property were inferior to those in Example 11.
    Example 7 added 1 part by weight of fluororesin to 100 parts by weight of PBT resin, 60 parts by weight of glass fiber, 20 parts by weight of red phosphorus master, and 20 parts by weight of phenol resin, and thus the combustion time was shorter than that of Example 4. It was confirmed that the flame retardancy was improved.
    Example 8 added 2 parts by weight of silicon powder to 100 parts by weight of PBT resin, 60 parts by weight of glass fiber, 20 parts by weight of red phosphorus master, and 20 parts by weight of phenolic resin, and thus the combustion time was shorter than in Example 4. It was confirmed that the flame retardancy was improved.
    The flame-retardant resin composition of the present invention is a non-halogen-based flame-retardant resin composition, in which only the red phosphorus powder is difficult to improve the flame retardancy of polytetramethylene terephthalate, in particular, the coated red powder, and the master containing the red phosphorus coated on the surface. Combination of pellets and novolac-type phenolic resins has the effect of reducing the dropping during combustion and significantly shortening the combustion time. The use of a novolak-type phenolic resin in combination with red phosphorus specifically improves flame retardancy. Thus, desirable results cannot be obtained from fluorine-containing melamine cyanurate and thermoallyl diallyl phthalate, which have been frequently used as preparations. In addition, the present invention is a small amount of flame retardant, has a high flame retardancy, good mechanical properties and resin kneading processability, there is no problem of bleed out to the surface of the molded article by annealing, which is a problem when phosphate ester is used, The industrial value is very large.
    权利要求:
    Claims (10)
    [1" claim-type="Currently amended] (A) 100 parts by weight of a thermoplastic aromatic polyester resin,
    (B) 3 to 70 parts by weight of a novolac phenol resin, and
    (C) 1 to 15 parts by weight of the coated red phosphorus powder having a cured resin film
    Flame-retardant resin composition consisting of.
    [2" claim-type="Currently amended] The dicarboxylic acid component in which the thermoplastic aromatic polyester resin (A) is mainly composed of at least one dicarboxylic acid selected from the group consisting of terephthalic acid and 2,6-naphthalenedicarboxylic acid. The composition whose diol component is polyester or polyester elastomer which consists of an ester unit which is at least 1 sort (s) of diol chosen from the group which consists of ethylene glycol and tetramethylene glycol.
    [3" claim-type="Currently amended] The polyester according to claim 2, wherein the thermoplastic aromatic polyester resin (A) comprises a polyester or a hard segment composed mainly of tetramethylene terephthalate or tetramethylene-2,6-naphthalenedicarboxylate as the main repeating unit. The composition is an elastomer.
    [4" claim-type="Currently amended] The composition according to claim 1, wherein the weight average molecular weight of the novolac phenol resin (B) is in the range of 600 to 13,000.
    [5" claim-type="Currently amended] The cured resin according to claim 1, wherein the cured resin of the coated red phosphorus powder is a cured product of at least one curable resin selected from the group consisting of phenol resins, epoxy resins, unsaturated polyester resins, melamine resins, urea resins and aniline resins. Composition.
    [6" claim-type="Currently amended] The composition according to claim 1, wherein an inorganic compound selected from the group consisting of hydroxides of aluminum hydroxide, magnesium hydroxide, zinc hydroxide and titanium is dispersed in the cured resin of the coated red powder coating.
    [7" claim-type="Currently amended] The composition according to claim 1, wherein a coating of an inorganic compound selected from the group consisting of aluminum hydroxide, magnesium hydroxide, zinc hydroxide and titanium hydroxide is further present in contact with red phosphorus under the coating of the cured resin.
    [8" claim-type="Currently amended] The composition according to claim 1, wherein the average particle diameter of the coated red powder having a film of cured resin is in the range of 5 to 40 µm.
    [9" claim-type="Currently amended] The composition according to claim 1, wherein the inorganic filler is further contained in the range of 5 to 150 parts by weight.
    [10" claim-type="Currently amended] The composition according to claim 1, wherein the fluorine resin is further contained in the range of 0.01 to 10 parts by weight.
    类似技术:
    公开号 | 公开日 | 专利标题
    CN102264816B|2014-07-02|Glass fiber reinforced polyester compositions, methods of manufacture, and articles thereof
    JP5761177B2|2015-08-12|Flame retardant polylactic acid-based resin composition, molded product thereof, and production method thereof
    EP2455427B1|2013-09-25|Flame-retardant thermoplastic resin composition and molded article
    TWI407459B|2013-09-01|Insulated wires for use in electronic equipment, connection cable and the use thereof, electronic equipment and flame retardant thermoplastic composition
    US7700680B2|2010-04-20|Polyester compositions flame retarded with halogen-free additives
    EP2287243B1|2014-10-29|High flow polyester composition
    EP2588531B1|2015-09-09|Flame resistant polyester compositions, method of manufacture, and articles thereof
    JP3923441B2|2007-05-30|Flame retardant synthetic resin composition
    KR101230083B1|2013-02-05|Flame-retardant polyester composition
    US7812077B2|2010-10-12|Polyester compositions, method of manufacture, and uses thereof
    ES2300715T3|2008-06-16|Polyester based molding composition.
    JP5233063B2|2013-07-10|Resin composition and molded article comprising the same
    EP1709120B1|2008-09-17|Halogen-free flame-retarded polyester composition
    US4258153A|1981-03-24|Flame retarding polyester composition
    US8188172B2|2012-05-29|Polyester compositions, method of manufacture, and uses thereof
    JP6056757B2|2017-01-11|Flame retardant thermoplastic polyester resin composition and molded article
    US7851532B2|2010-12-14|Flame retardant thermoplastic polyester resin composition
    US6710108B2|2004-03-23|Flame-retardant polyester composition, method for the preparation thereof, and articles derived therefrom
    US20120322923A1|2012-12-20|Flame retardant composition for thermoplastic molding compounds
    EP0516351B1|1997-10-15|Flame-retardant polybutylene terephthalate resin composition
    KR101698874B1|2017-01-23|Flame resistant polyester compositions, method of manufacture, and articles thereof
    CA2456237A1|2003-02-20|Halogen-free flameproof polyester
    WO2005061626A1|2005-07-07|Flame resistant thermoplastic resin composition
    KR930007700B1|1993-08-18|Flame retardant polyester resin composition
    US7612130B2|2009-11-03|Composition of polyester, aromatic epoxy compound and epoxy-functional polyolefin and/or copolyester
    同族专利:
    公开号 | 公开日
    DE69813094D1|2003-05-15|
    TW477807B|2002-03-01|
    KR100519571B1|2005-12-21|
    WO1998030632A1|1998-07-16|
    US6133358A|2000-10-17|
    EP0889094A1|1999-01-07|
    EP0889094B1|2003-04-09|
    EP0889094A4|1999-05-06|
    DE69813094T2|2003-12-11|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    法律状态:
    1997-01-10|Priority to JP97-3021
    1997-01-10|Priority to JP302197
    1998-01-06|Application filed by 야스이 쇼사꾸, 데이진 가부시키가이샤
    1998-01-06|Priority to PCT/JP1998/000013
    2000-11-06|Publication of KR20000064569A
    2005-12-21|Application granted
    2005-12-21|Publication of KR100519571B1
    优先权:
    申请号 | 申请日 | 专利标题
    JP97-3021|1997-01-10|
    JP302197|1997-01-10|
    PCT/JP1998/000013|WO1998030632A1|1997-01-10|1998-01-06|Flame-retardant resin composition|
    [返回顶部]