• 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:
    1. Fire retardant composition for rigid polyurethanes, including dimethyl methylphosphonate, characterized in that, in order to prevent delamination and warping of poly. urethane, as well as neutralizing impurities trimethylphosphite, it additionally contains three (aryl / alkyl) phosphate selected from the group including three (isopropylphenyl) phosphate. tricresyl phosphate, trixilyl phosphate, trimethyl phosphate or diphenyl isodecyl phosphate, at a mass ratio of dimethyl methyl phosphonate and tri (aryl / alkyl) phosphate, equal to 10-90: 10-90. 2. The composition according to claim 1, characterized by the fact that it contains phosphonate and phosphate with a mass ratio of 10-40: 60-90, respectively. 3.Composition according to Claim. 1, and is distinguished with the fact that it further comprises anti gapoidsoderzhaschy pyrene, vybranny from the group consisting of pentabromodiphenyl ether, ester bromkrezilglitsidilovy di-, tetra- brombisfenol A geksabromp 1klodode- CAD or dibromneopentilglikol as 8-100% based on the weight of the mixture of phosphonate and phosphate. 4. A method of preparing a flame retardant for rigid polyurethanes, characterized in that the dimethyl methyl phosphonate and three (aryl / alkyl) phosphate are mixed and the mixture is held at 20-70 ° C for 12-48 hours. § (L o 9e
    公开号:SU1210662A3
    申请号:SU833655364
    申请日:1983-10-11
    公开日:1986-02-07
    发明作者:Левитт Бузард Дэвид；Джон Деллар Ричард
    申请人:Циба-Гейги Аг (Фирма)；
    IPC主号:
    专利说明:

    one
    This invention relates to a flame retardant composition for use in rigid polyurethanes and a process for its preparation.
    The purpose of the invention is to prevent delamination and warping of polyurethane, as well as neutralization of trimethyl phosphite impurity.
    The invention is illustrated by few examples and tables in which parts and percentages are given by weight.
    Example 1. 10 h of crude methylphosphinic acid dimethyl ester (DMMP) containing 1% trimetyphosphite are added to 90 h three (isopropylphenyl) phosphate with a phosphorus content of 8.4%. When stored in a glass bottle at room temperature for 12-24 hours, no odor of trimethyl phosphite was detected.
    Example 2. The composition is prepared analogously to example 1, except that the mixture is held at 70 C. The mixture loses the smell in less than 12 hours.
    Example 3. A mixture of 40 parts of raw DMSH from example 1 and 60 hours of three (of propylphenyl) phosphate is heated at 70 ° C, after 12-30 hours the mixture does not contain trimethyl phosphite.
    Example 4. 90 parts containing 0.05% trimethyl phosphite are added to 10 parts of the phosphate from Example 1. When stored at room temperature, the mixture completely loses the smell for 24 hours.
    Example 5. A formulation was prepared as described in Example 4 using DMMP containing 0.1% trimethyl phosphite. The mixture loses odor between 24 and 48 h.
    Example 6. The procedure of Example 4 is repeated, except that the mixture is heated at 70 ° C. Full deodorization takes place at the limit of 20 hours.
    Examples 7-10. The formulations are prepared as in example 1 with the exception that the phosphate is replaced by other phosphoric esters of the required purity given in table. one.
    Example 11-12. Get polyurethane with a density of foam 30t + kg / m based on the following composition, including:
    Propylam RF 132 100 Dimethyldaclohexyl-amine 1,8
    622
    oi - Methylstyrene Dabco 33LV Silicone Surfactant
    substance
    Trichlorofluoromethane Fireproofing Agent
    Izokon M
    0.2 0.1
    2.0
    33
    As noted
    below
    126.9
    Propylam RF 132 is the brand name of polystyrene sucrose condensate with propyl oxide; Dabco 33LV is a tertiary amine used in
    as a catalyst; isocon-polymeric diphenylmethane diisocyanate.
    These components are mixed at room temperature using a high-speed mixer (2000 rpm),
    the isocyanate is added last, and then immediately placed in a cardboard form. Due to the ongoing s (kzothermic reaction, free foam is allowed to rise. It takes place from the moment the isocyanate is added until the creamy consistency mixture is obtained. This is the cream formation time. The time needed for the foam to reach maximum height is called the rise time. The foam loses its stickiness, called the loss of stickiness. After the stickiness is lost, the foam is held three times at room temperature.
    After three days of storage, samples are cut out of the foam, which are subjected to a limited oxygen test and tested for horizontal burning. The results are shown in Table. 2, for comparison, the same penny material is obtained without the use of a flame retardant agent. Foams obtained in
    examples 11 and 12, do not have the tendency to delamination and warping.
    Examples 13 to 15. For example 11, receive polyurethane foam density of 36 ± 1 kg / m using the following composition, including:
    Propylene RF 176 Water
    Polyurax SR 242 Flame Retardant
    Trichlorofluoromethane Isokon M
    100
    1.1 2.2
    Below
    35
    134.7
    .Polyurax SP 242 - firm name of surface-active substance
    Samples were cut from the resulting foams and tested for a limited oxygen index. The results are shown in Table. 3
    The foam obtained in examples 13-16, do not have a tendency to exfoliation and warping.
    Example 17. In Example 11, except that a composition containing 10 parts of the product of example 3 and 10 parts of dibromoneopentyl glycol is used as a flame retardant, polyurethane foam is prepared with an oxygen indicator of 23.1%, which does not have a propensity to exfoliation and co-feed.
    Tricresyl phosphate Trimethyl phosphate Trixilyl phosphate Diphenylisodecyl phosphate
    Example 18. Receive polyurethane foam according to example 11, for - except. It is based on the fact that a mixture of 13 parts of the product from example 3 and 7 parts of hexabromocyclo-dodecane and a mixture of 10 parts of the product from example 3 and 10 parts of dibromo-neopentyl glycol are used as antipyrene. The oxygen ratio of polyurethane foam is 24.2% and 24.9%, respectively.

    Example 19 (comparative) Polyurethane foam is obtained in the same way as described, but only DMF in an amount of 10 hours is used as a flame retardant. Exfoliation and warping of a polyurethane foam product is observed.
    Table
    48 48 24-24
    23 23 70 70
    Table 2
    Table 3
    权利要求:
    Claims (4)
    [1]
    1. Fire retardant composition for rigid polyurethanes, including dimethyl methylphosphonate, characterized in that, in order to prevent delamination and warpage of the polyurethane, as well as to neutralize the trimethylphosphite impurity, it additionally contains three (aryl / alkyl) phosphate selected from the group comprising three ( isopropylphenyl) phosphate, tricresyl phosphate, trixyl phosphate, trimethyl phosphate or diphenyl isodecyl phosphate, with a mass ratio of dimethyl methyl phosphonate and tri (aryl / alkyl) phosphate equal to 10-90: 10-90.
    [2]
    2. The composition of the pop. 1, characterized in that it contains phosphonate and phosphate at a mass ratio of 10-40: 60-90, respectively.
    [3]
    3. The composition of the pop. 1, characterized in that it additionally contains a halogen-containing flame retardant selected from the group consisting of pentabromodiphenyl ether, dibromocresyl glycidyl ether, tetrabromobisphenol A, hexabromocyclododecane or dibromneopentyl glycol, as 8-100% based on the phosphate mass.
    [4]
    4. A method for producing a flame retardant for rigid polyurethanes, characterized in that dimethyl methylphosphonate and tri (aryl / alkyl) phosphate are mixed and. the mixture is kept at 20-70 C for 12-48 hours.
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    同族专利:
    公开号 | 公开日
    AU2000683A|1984-04-19|
    DK467683A|1984-04-13|
    JPH0449580B2|1992-08-11|
    CA1236621A|1988-05-10|
    DE3367782D1|1987-01-08|
    DK467683D0|1983-10-11|
    EP0108713A1|1984-05-16|
    BR8305616A|1984-05-15|
    EP0108713B1|1986-11-20|
    US4565833A|1986-01-21|
    HK60589A|1989-08-04|
    AU566134B2|1987-10-08|
    ZA837544B|1984-09-26|
    SG12889G|1990-10-26|
    AT23722T|1986-12-15|
    JPS5991116A|1984-05-25|
    引用文献:
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    GB1094717A|1962-12-31|1967-12-13|Hooker Chemical Corp|High density polyurethane foams|
    GB1146173A|1966-06-18|1969-03-19|Geigy Uk Ltd|Production of triaryl phosphates|
    AR206903A1|1973-11-12|1976-08-31|Stauffer Chemical Co|COPOLICONDENSATION PRODUCT OF A TRIS-BETA-HALOALKYLPHOSPHATE AND A DIALKYL PHOSPHONATE USEFUL AS A FIRE RETARDING AGENT|
    US4165411A|1975-06-18|1979-08-21|W. R. Grace & Co.|Flame retardant urethane and method|
    DE2610180C3|1976-03-11|1978-09-14|Akzo Gmbh, 5600 Wuppertal|Process for the flame-retardant finishing of textiles|
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    EP0240806B1|1986-04-07|1992-07-01|Chemische Fabrik Kalk GmbH|Reactive fire-protective formulation for rendering polyurethane rigid foam materials flame-resistant and process for preparing same|
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    US4746682A|1987-04-01|1988-05-24|Fmc Corporation|Polyurethane flame retardant|
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    US4983654A|1987-12-28|1991-01-08|Ford Motor Company|Phosphate/epoxy stabilizer for extrudable polyester blends|
    JPH0284421A|1988-06-04|1990-03-26|Achilles Corp|Impact-absorptive polyurethane foam and production thereof|
    JPH02163160A|1988-12-15|1990-06-22|M D Kasei Kk|Molded polyurethane product|
    US5082867A|1989-09-28|1992-01-21|Great Lakes Chemical Corporation|Flame retardant flexible polyurethane foam compositions|
    US5547614A|1989-11-14|1996-08-20|Akzo Nobel N.V.|Flame retardant mixture of polybrominated diphenyl oxide and organic diphosphate|
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    CA2063812A1|1990-06-01|1991-12-02|James J. Anderson|Phosphate ester flame retardant mixture and foamed resins containing same|
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    US5391583A|1992-07-17|1995-02-21|Blount; David H.|Flame-retardant polyproducts|
    DE4225765C1†|1992-08-04|1993-09-16|Bayer Ag, 51373 Leverkusen, De|
    JPH08506370A|1993-02-10|1996-07-09|ラソアー・アクチェン・ゲゼルシャフト|Prepolymer composition for insulating foam|
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    US6667355B2|2001-08-30|2003-12-23|Pabu Services, Inc.|Higher alkylated triaryl phosphate ester flame retardants|
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    法律状态:
    优先权:
    申请号 | 申请日 | 专利标题
    GB8229075|1982-10-12|
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