• 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:
    The present invention relates to modified polyols, and more particularly to polyols modified with polyisocyanates that can be employed, among other things, as components for formulations for polyurethanes or polyurethanes-isocyanurates.
    公开号:SU900816A3
    申请号:SU772501308
    申请日:1977-07-08
    公开日:1982-01-23
    发明作者:Фатутто Пьерлуиджи
    申请人:Монтэдисон С.П.А. (Фирма)；
    IPC主号:
    专利说明:

    (5) METHOD FOR OBTAINING A PREPOLYMER WITH END
    one
    The invention relates to methods for producing intermediates for producing polymers, in particular, to a method for producing prepolymer with terminal hydroxyl groups, which can be used as a component in the preparation of polyurethanes or polyisocyanuraturethanes.
    A known method for producing a prepolymer with terminal 1 hydroxyl by fcl groups based on diisocyanates and glycols using the Cl coupling method.
    However, the synthesis is carried out under stringent conditions.
    Closest to the invention in its technical essence is a method for preparing a prepolymer with terminal hydroxyl groups by reacting an excess of the hydroxyl-containing compound with the isocyanate component. Combine flexible and rigid blocks in the synthesis of polyurethanes, it is possible to obtain polyhydroxyl groups based on hydroxyl-containing prepolymer
    urethane with a wide range of properties 21.
    However, due to the relative reactivity of the prepolymer 5, the viability of the composition based on it is reduced.
    The purpose of the invention is to reduce the reactivity of the prepolymer and to ensure the self-extinguishing properties of the final product based on the prepolymer.
    The goal is achieved by the fact that upon receipt of a prepolymer with terminal hydroxyl groups
    15 by reacting an excess of a hydroxyl-containing compound with the isocyanate component, monopropylene glycol of equivalent weight is used as the hydroxyl-containing compound.
    3Q 38 or diethyl glycol of equivalent weight 53 and polymethylene diphenle diisocyanate of equivalent weight} kQ is used as the isocyanate component at a weight ratio of 25 SRI g /: and oxyl-containing compound
    and the isocyanate component, equal to 2: 1, and with an equivalent ratio of OH / NCO-rpynn, equal to (.5): 1
    The diols that are used according to the invention are of the type of diols having a linear or branched paraffin chain, or of the ether type, with two free hydroxy groups, both primary or both secondary, or one primary and one secondary.
    Typical examples of such compounds are monopropylene glycol (OH-CH (CH) -CHj, OH) and diethylene glycol (OH-CHj, -CHi-0-CHj-CHj, -OH).
    Polyisocyanates are selected from a wide range of bi or polyfunctional products, preferably of the aromatic type. Typical examples of such polyisocyanates are 2, -and / or 2,6-toluene diisocyanate (TD1): 4,4-diphenyl methane diisocyanate (MOZ) and polyphenyl polymethylene polyisocyanates (crude CRUDE HDZ).
    Hydroxy-terminated prepolymers are usually medium or high viscosity liquids containing a certain amount of free OH and NH groups. The amount of free OH groups depends on the diol / polyisocyanate ratio and the reaction conditions.
    These products partially satisfy the requirement for use as a polyol component in the preparation of polyurethanes or isocyanurates polyurethanes. For these purposes, they are used as substitutes or in a mixture with commonly used polyols.
    Example 1. 1000 g of monopropylene glycol (equivalent weight 38) are placed at 25 ° C and a 3-liter glass flask is added, with stirring, 100 g of CRUDE (polymethylenediphenyl diisocyanate,
    having an equivalent weight of 1W). A cream colored emulsion is formed at the reaction night. Then, after 10 minutes of stirring, during which the temperature rises to, the liquid becomes an amber transparent color. Then QQ g CRUDE MDJ is gradually added with stirring, stirring is carried out until the liquid becomes clear again.
    The weight ratio between monopropylene glycol and isocyanate 2: 1,
    At the same time as the equivalent ratio. Thus, the prepolymer obtained has a density of 1–13 g / cm, a viscosity of 10,000 centipoise at, an equivalent weight of 66 relative to the OH groups only, and 57 relative to the sum of OH + NH.
    Example 2. 1000 g of diethylene glycol (equivalent weight 53} is placed in a one-liter glass flask, and 100 g CRUDE HDJ (equivalent weight fiO) is added thereto with stirring.
    A cream colored emulsion is formed at the beginning of the reaction. Then, after 10 minutes of stirring, during which the temperature rises to 60 ° C, the liquid becomes clear, amber. Then, while stirring, 400 g of CRUDE MDZ are added and stirring is continued until the liquid becomes clear again.
    The weight ratio between diethylene glycol and isocyanate is 2: 1, the equivalent ratio is 5 ,.
    The resulting polyol has a Brookfield 9000 cPz density of 1.18 viscosity at 20 ° C; equivalent weight is 98 relative to OH and 79.5 relative to the sum of OH + NH.
    Example 3 The process is carried out as in Example 2, but using a glycol / isocyanate weight ratio of 100/35 and an equivalent ratio of 7.5: 1. Thus, the obtained prepolymer has an equivalent weight of 91.7 with respect to the groups OH and 79.3 with respect to the sum of OH + NH. Brookfield viscosity 1368 cPz at 25 and a density of 1.18 g / cm at 22 ° C.
    The invention makes it possible to significantly reduce (in some cases, eliminate) the use of flame retardant additives, even obtaining self-extinguishing products or products in a low burning rate.
    Formula Invention
    The method of producing prepolymer with terminal hydroxyl groups by reacting an excess of the hydroxyl-containing compound with the isocyanate component, characterized in that, in order to reduce the reactivity of the prepolymer and to provide self-extinguishing
    5,900,8164
    properties of the final product, in ka-sources of information,
    monocropylene glycol is used as a hydroxyl-containing compound taken into account when examining
    equivalent weight 38 or diethylene- 1. Kegp W ,, Rauter Kus K.J.,
    glycol equivalent weight 53, and $ Weber W, Makrcjmol Cbem, 19b1,
    as an isocyanate component i3 P.98.
    polymethylenediphenyldiso-2 is used. Lipatnikov N.A., Gritsenko T.M. cyanate of equivalent weight b in priRazilevska NP and Zhivotova A.I. weight ratio of hydroxylsoder-. Study of the reaction of the hexamethylene compound and isocyanate diisocyanate with ethylene glycol, the Syncomponent, equal to 2: 1, and with equivalence and physicochemical polymers (Polyvalent ratio of OH / NCO groups, urethanes), Kiev, p.96 equal to (5.3-7.5): 1. (prototype).
    权利要求:
    Claims (1)
    [1]
    Claim
    A process for preparing a prepolymer with terminal hydroxyl groups by reacting an excess of a hydroxyl compound with izotsia 55 adjusted to room component, characterized in that, to reduce the reactivity of the prepolymer and to provide self-extinguishing properties of the final product as a hydroxyl-connect couplings are used monopropylene equivalent weight of 38 or diethylene glycol equivalent weight 53, and as isocyanate component use polymethylene diphenyl diisocyanate of equivalent weight 140 pr the weight ratio of hydroxyl-containing compound and the isocyanate component is 2: 1, and at an equivalent ratio of OH / NCO-groups is equal to (5.3 ~ 7.5): 1.
    类似技术:
    公开号 | 公开日 | 专利标题
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    CA2049515A1|1992-02-23|Polyisocyanate mixtures containing isocyanurate groups, a process for their production and their use for the production of polyurethane foams
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    US5356943A|1994-10-18|Rigid foams
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    US4525590A|1985-06-25|Simplified process for the production of polyamines by the alkaline hydrolysis of compounds containing NCO-groups
    US3584085A|1971-06-08|Phosphoramidates
    US3692707A|1972-09-19|Prepolymers and fire retardant polyurethanes therefrom
    CA2086652C|2003-12-16|Liquid, light-colored poylisocyanate mixtures and a process for their production
    US3943077A|1976-03-09|Fire retardant polyurethane foams
    US4397966A|1983-08-09|Alkylene oxide adducts of vicinal toluenediamine
    US4762950A|1988-08-09|Selective oxyalkylaton of N-|-aniline
    同族专利:
    公开号 | 公开日
    NO145245C|1982-02-10|
    FR2357590B1|1980-03-14|
    FR2357590A1|1978-02-03|
    ES460546A1|1978-05-16|
    BE856610A|1978-01-09|
    NO145245B|1981-11-02|
    JPS539741A|1978-01-28|
    US4120834A|1978-10-17|
    IT1064599B|1985-02-18|
    NL7707427A|1978-01-11|
    CA1114990A|1981-12-22|
    SE7707853L|1978-01-10|
    DE2731012A1|1978-01-12|
    NO772378L|1978-01-10|
    CS198260B2|1980-05-30|
    GB1589583A|1981-05-13|
    DK301677A|1978-01-10|
    FI772100A|1978-01-10|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    US9957347B2|2013-02-25|2018-05-01|Basf Se|Reduced discoloration of thermoplastic polyurethanes based on polymer polyols via incorporation of aliphatic isocyanates|US2948691A|1951-05-10|1960-08-09|Mobay Chemical Corp|High molecular weight polyether urethane polymers|
    BE589613A|1959-04-10|
    GB1448933A|1974-02-14|1976-09-08|Shell Int Research|Process for preparing polyurethane products|DE2834623A1|1978-08-08|1980-02-28|Bayer Ag|STABILIZED FUEL SUSPENSIONS IN POLYOLS|
    US4288577A|1979-12-14|1981-09-08|E. I. Du Pont De Nemours And Company|Novel urethanediols and polyurethanes therefrom|
    EP0045413A1|1980-07-31|1982-02-10|Basf Wyandotte Corporation|Flexible polyurethane foam compositions and methods for the preparation|
    DE3110724A1|1981-03-19|1982-10-07|Bayer Ag, 5090 Leverkusen|SOLUTIONS OF OLIGOURETHANE ETHERS IN POLYETHERPOLYOLS AND THE USE THEREOF IN A METHOD FOR THE PRODUCTION OF POLYURETHANE FOAMS WITH GOOD HIGH-FREQUENCY WELDABILITY AND GOOD FLAME-LASABILITY|
    US4489177A|1983-12-29|1984-12-18|Olin Corporation|Isocyanate-reactive compounds from TDI distillation residue and polyurethanes prepared therefrom|
    US4546122A|1984-08-06|1985-10-08|Mobay Chemical Corporation|Flexible polyurethane foams|
    JPH0568409U|1991-03-08|1993-09-17|日本利器工業株式会社|Nail clipper|
    EP3498745A1|2017-12-18|2019-06-19|Covestro Deutschland AG|Flame retardant rigid polyurethane foams|
    法律状态:
    优先权:
    申请号 | 申请日 | 专利标题
    IT25181/76A|IT1064599B|1976-07-09|1976-07-09|MODIFIED POLYOLS|
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