Classifications

• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G18/00—Polymeric products of isocyanates or isothiocyanates
  • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
  • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
  • C08G18/40—High-molecular-weight compounds
  • C08G18/48—Polyethers
  • C08G18/50—Polyethers having heteroatoms other than oxygen
  • C08G18/5021—Polyethers having heteroatoms other than oxygen having nitrogen
  • C08G18/5024—Polyethers having heteroatoms other than oxygen having nitrogen containing primary and/or secondary amino groups
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G18/00—Polymeric products of isocyanates or isothiocyanates
  • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
  • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
  • C08G18/40—High-molecular-weight compounds
  • C08G18/4009—Two or more macromolecular compounds not provided for in one single group of groups C08G18/42 - C08G18/64
  • C08G18/4072—Mixtures of compounds of group C08G18/63 with other macromolecular compounds
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G2110/00—Foam properties
  • C08G2110/0025—Foam properties rigid
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G2110/00—Foam properties
  • C08G2110/0041—Foam properties having specified density
  • C08G2110/005—< 50kg/m3
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G2110/00—Foam properties
  • C08G2110/0083—Foam properties prepared using water as the sole blowing agent

Definitions

• the present invention relates to a polyol blend for the preparation of open cell rigid polyurethane foams, to a process for preparing open cell rigid polyurethane foams, to the polyurethane foams obtainable by this process and to shaped articles comprising these polyurethane foams.
• rigid polyurethane foams are well known for their excellent heat insulating properties.
• Particularly closed cell polyurethane foams are widely used as heat insulating material in e.g. pipings, storage tanks, buildings and refrigerators.
• Closed cell polyurethane foams used to be made with blowing agents based on chlorofluorocarbons (CFC's) of which R-ll ( trichlorofluoromethane) was a frequently applied example.
• CFC's chlorofluorocarbons
• R-ll trichlorofluoromethane
• the heat insulating properties were for a large part determined by the thermal conductivity of CFC gases, which filled the cells of the foam.
• Alternative blowing agents have been investigated and are actually used, but is very difficult to find substitutes for CFC as a blowing agent, which have equally low thermal conductivity properties.
• open cell rigid polyurethane foams have not such excellent heat insulating properties as closed cell rigid foams, their thermal conductivity is still sufficient to be useful as a heat insulating material. Furthermore, the dimensional stability at low foam density of open cell foams is better than that of closed-cell foams. Open cell rigid polyurethane foams, accordingly, are very suitable for application as the core material in vacuum insulation panels. Such panels usually comprise a core material enclosed in a vacuum container of metal and/or plastic films. Furthermore, open cell rigid polyurethane foams can be used in those rigid foam applications, which do not require any heat insulating properties, but which do require some structural support, for instance, use for automotive headliners or packaging. Several methods have been proposed to prepare open cell rigid polyurethane foams.
• a method for preparing open cell rigid polyurethane foams wherein a polymethylene polyphenylisocyanate prepolymer with a polyol at an NCO/OH equivalent ratio of 1.3 to 3.0 using water as the sole blowing agent in the presence of a catalyst, a foam stabiliser and a cell opening agent.
• the cell opening agent suitably is a divalent metal salt of a fatty acid, such as calcium stearate, magnesium stearate, strontium stearate or calcium myristate.
• open cell rigid polyurethane foams are prepared by using water as a blowing agent in combination with a specific polyol mixture comprising two or three polyols having different hydroxyl values, said mixture having a hydroxyl value of 160-360 mg KOH/g.
• an open cell rigid polyurethane foam is prepared by reacting a polyol with a prepolymer obtained by reacting polymethylene polyphenyl polyisocyanate with a monohydric alcohol using a CFC-substitute as blowing agent in the presence of a catalyst, a foam stabiliser and a cell opening agent.
• the cell opening agent suitably is a divalent metal salt of a fatty acid, such as calcium stearate.
• a method for producing open cell rigid polyurethane foams is disclosed, wherein the open cell structure is achieved by using a specific anti- foaming agent (viz. Tegostab 8919; Tegostab is a trademark) in combination with an appropriate silicone surfactant .
• a specific anti- foaming agent viz. Tegostab 8919; Tegostab is a trademark
• open cell rigid polyurethane foams could be provided having a very low density in combination with good mechanical or structural stability, as such low density foams are attractive for use in a wide variety of applications including the application as heat insulating material.
• the low density is especially desired, because the low weight of the foam facilitates transportation and handling of e.g. insulation panels.
• a lower density also means that less starting material is necessary to prepare the same volume of foam as compared to the situation in which a higher density foam is to be prepared. Clearly this is advantageous from an economic perspective.
• low density open cell rigid foams could be prepared without needing any cell-opener or anti-foaming agent, thus facilitating the manufacture whilst still obtaining excellent foams.
• the present invention relates to a polyol blend comprising:
• a polymer polyol comprising a polymer stably dispersed in a base polyol medium, which base polyol medium has an average primary hydroxyl content of less than 20%.
• the present invention combines a rigid polyol component (component (a) ) with a particular polymer polyol (component (b) ) , which is normally used in the manufacture of flexible polyurethane foams .
• This specific combination of polyols has been found to result in open cell rigid foams having excellent properties without the need to apply cell-opening agents or anti- foaming agents.
• the quantities in which the polyol and the polymer polyol are used may vary within broad limits, but preferably the polyol blend according to the present invention comprises 2 to 25 parts by weight, more preferably 2 to 10 parts by weight, of polymer polyol (b) per 100 parts by weight of polyol component (a) .
• the polyol component (a) can be any rigid polyol or combination of rigid polyols having an average hydroxyl value of 150 to 850 mg KOH/g. Such rigid polyols are known in the art.
• polyoxyalkylene polyols have a nominal molecular weight of from 300 to 1500, suitably 500 to 1000, and a nominal average functionality of at least 2.0, suitably from 2.5 to 6.
• the average hydroxyl number preferably has a value in the range of from 150 to 650 mg KOH/g.
• the polyol component (a) may comprise a single rigid polyol, but may also comprise two or more rigid polyols.
• the polyol component (a) comprises a polyol having a hydroxyl value of 150 to 400 mg KOH/g and a polyol having a hydroxyl value of 400 to 650 mg KOH/g.
• a rigid polyol having a lower hydroxyl value is CARADOL GB250-01, while examples of rigid polyols having a higher hydroxyl value are
• CARADOL LP530-03 and CARADOL LP585-01 (CARADOL is a trademark) .
• the polymer polyol used as component (b) may m principle be any polymer polyol comprising a polymer stably dispersed in a base polyol medium, provided the base polyol medium has an average primary hydroxyl content of less than 20% based on the total of hydroxyl groups present on the polyol (s) forming the base polyol medium. Accordingly, the base polyol medium may consist of one or more polyols provided the average primary hydroxyl content of these polyol (s) is less than 20%, preferably less than 10% and most preferably less than 5%.
• the polymer polyol component (b) suitably comprises such a base polyol medium and a polymer stably dispersed therein in an amount of 5 to 40% by weight based on total weight of polymer polyol.
• the base polyol medium consists of a polyoxyalkylene polyol having a molecular weight m the range of from 250 to 12,000, preferably from 500 to
• base polyol medium most preferably has a very low average primary hydroxyl content
• very good base polyols are those having a very low ethylene oxide (EO) content resulting from EO tipping.
• EO ethylene oxide
• the ethylene oxide content resulting from ethylene oxide tipping is less than 1% by weight, while most suitably the polyol has not been tipped with EO at all.
• the polymer which is stably dispersed in the base polyol medium, may in principle be any such polymer known to be applicable for this purpose.
• suitable polymers include the polymers based on ethylenically unsaturated monomers and particularly polymers of vinyl aromatic hydrocarbons, like styrene, alpha-methyl styrene, methyl styrene and various other alkyl- substituted styrenes . Of these, the use of styrene is preferred.
• the vinyl aromatic monomer may be used alone or in combination with other ethylenically unsaturated monomers, such as acrylonitrile, methacrylonitrile, vinylidene chloride, various acrylates and conjugated dienes like 1, 3-butadiene and isoprene.
• Preferred polymers are polystyrene and styrene- acrylonitrile (SAN) copolymers.
• Another suitable class of polymers are the polyurea and polyurethane polymers. Particularly the condensation products of polyhydric alcohol amines and aromatic diisocyanates are very useful in this respect.
• a very much preferred polymer is the condensation product of triethanol amine and toluene diisocyanate (TDI) .
• the dispersed polymer is polystyrene, SAN copolymer, polyurea or the polyurethane polymer obtained as the condensation product of triethanolamine and toluene diisocyanate.
• the dispersed polymer is suitably present in an amount of from 5 to 40% by weight based on total weight of polymer polyol.
• polymer is polystyrene or SAN polymer
• preferred amounts are between 5 and 35% by weight, whilst in case of polyurea polyurethane polymers the preferred amount of polymer is between 5 and 20% by weight .
• the polyol blend according to the present invention is very suitable for the preparation of open cell rigid polyurethane foams.
• the present invention also relates to a process for the preparation of open cell rigid polyurethane foams, which process comprises reacting the polyol blend described herein before with a polyisocyanate component in the presence of at least a catalyst, a foam stabilising agent and a blowing agent.
• Polyisocyanates that may be used are those conventionally applied in the production of rigid polyurethane foams.
• Useful polyisocyanates should contain at least two isocyanate groups and include both aliphatic -usually alkylene- and aromatic di-, tri-, tetra- and higher isocyanates known in the art to be suitably applied in the production of rigid polyurethane foams . Mixtures of two or more of such aliphatic and/or aromatic polyisocyanates may also be applied.
• suitable polyisocyanates include 2,4-toluene diisocyanate (2,4-TDI), 2,6-TDI, mixtures of 2,4-TDI and 2,6-TDI, 1, 5-naphthene diisocyanate, 2, 4-methoxyphenyl diisocyanate, 4 , 4 ' -diphenylmethane diisocyanate (MDI), 4 , 4 ' -biphenylene diisocyanate, 3, 3 ' -dimethoxy-4 , 4 ' -bi- phenylene diisocyanate, 3 , 3 ' -dimethyl-4 , 4 ' -biphenylene diisocyanate and 3, 3 ' -dimethyl-4 , 4 ' -diphenylmethane diisocyanate, 4 , 4 ' , 4 "-triphenylmethane triisocyanate, 2, 4 , 6-toluene triisocyanate
• polymeric MDI a mixture of polyisocyanates with MDI as the main component, may also be used.
• polymeric MDI a mixture of polyisocyanates with MDI as the main component
• the quantity of polyisocyanate component to be used should suitably be such that the isocyanate index has a value between 50 and 150, most suitably between 80 and 130. However, isocyanate indices outside these ranges may also be used.
• Catalysts for the production of rigid polyurethane foams are known in the art and include many different compounds.
• suitable catalysts include tertiary amines, such as, for instance, bis (2 , 2 ' -dimethylamino) ethyl ether, trimethylamine, triethylamine, triethylenediamine and dimethylethanolamine (DMEA).
• Tin-based catalysts may also be applied and include tin salts and dialkyl tin salts of carboxylic acids. Specific examples are dibutyltin dilaureate, stannous octoate, stannous oleate, dibutyltin acetate and dibutyltin diacetate.
• trimerisation catalysts like potassium acetate may be applied.
• the catalyst is typically used in an amount of from 0.01 to 7 php (parts by weight per 100 parts of polyol) .
• the foam stabiliser (or surfactant) used in the present process may be any polyurethane foam stabiliser useful in the production of rigid polyurethane foams.
• Organosilicone or organopolysiloxane surfactants are most conventionally applied as foam stabilisers in polyurethane production. A large variety of such surfactants is commercially available. Usually, such foam stabiliser is used in an amount of up to 3 php.
• blowing agent is also present in the process according to the present invention.
• Suitable blowing agents include water, aceton, (liquid) carbon dioxide, halogenated hydrocarbons, aliphatic alkanes, such as n- pentane and isopentane, and alicyclic alkanes, such as cyclopentane and cyclohexane . It will be understood that these blowing agents may be used singly or in mixtures of two or more.
• water it has been found particularly advantageous to use water as the sole blowing agent.
• the amount in which the water is used may vary between wide limits, but very good results have been achieved when using water in an amount of 2-12 php.
• the present invention relates to an open cell rigid polyurethane foam obtainable by the process described herein before, which polyurethane foam has a density of less than 50 kg/m.3 and a closed cell content of less than 10%, preferably of less than 5%.
• Preferred foams, which are obtainable by the present process have densities of 10 to 30 kg/m ⁇ , more preferably 10 to 25 kg/m.3.
• the present invention also relates to shaped articles comprising the open cell rigid polyurethane foam defined in the preceding paragraph as well as to heat insulating materials comprising this open celled rigid polyurethane foam in a laminate structure.
• the components used in the examples are: Polyol components
• Polyol A A rigid, aromatic, amine-group containing, propylene oxide (PO) -based polyether polyol having a hydroxyl value of 530 mg KOH/g.
• Polyol B A rigid, glycerol initiated polyether polyol having a hydroxyl value of 250 mg KOH/g.
• PP-A A polymer polyol containing (i) a base polyol being a EO/PO based, glycerol initiated polyether polyol having a primary hydroxyl content of essentially 0%, a molecular weight of 3500 and a hydroxyl value of 37 mg KOH/g and (ii) stably dispersed therein 20 wt% polystyrene.
• PP-B A polymer polyol containing (i) the same base polyol as PP-A, and (ii) stably dispersed therein 40 wt% styrene-acrylonitrile copolymer .
• PP-C A polymer polyol containing (i) a base polyol being a EO/PO based, glycerol initiated polyether polyol having a primary hydroxyl content of 80%, a molecular weight of 4700 and a hydroxyl value of 25 mg KOH/g and containing 14 wt% EO-tip and (ii) stably dispersed therein 28 wt% polystyrene.
• PP-D A polymer polyol containing (i) the same base polyol as PP-C, and (ii) stably dispersed therein 15 wt% styrene-acrylonitrile copolymer .
• TCPP tris (chloropropyl) phosphate (flame retardant)
• a polyol formulation was prepared consisting of
• the formulation was allowed to foam in a bag. After foaming a sample of the foam was taken and density and closed cell content were determined.
• Example 1 was repeated except that 10 pbw of PP-B were added (Ex-2) in stead of PP-A.
• composition of the foaming formulation and the properties of the resulting foam are indicated in
• Example 1 was repeated except that 10 pbw of PP-C (CEx-1) or 10 pbw of PP-D (CEx-2) were used in stead of 10 pbw of PP-A.
• composition of the foaming formulations and the properties of the resulting foam are indicated in Table I.
• a laminate with a open cell polyurethane foam prepared with a polyol blend according to the present invention was made on a continuous laminator machine.
• the laminator machine is a high pressure, multi- component unit, manufactured by Cannon/Viking UK.
• the urethane system being a blend of four different streams, was dispensed on the bottom facing through a perforated pipe, fitted to a traversing mixing head.
• As the facing polyethylene coated kraft paper was used.
• the machine output was adjusted to produce 60 mm thick, 600 mm wide laminates at an overall target density of 22 kg/m3 a t a belt speed of 2.9 m/min.
• the 6 meter conveyor section was working in free rise mode.
• polyol blend As stated above, four streams (denoted as “polyol blend”, “cat 1 blend”, “cat 2 blend” and “MDI”) are pumped into the mixing head, where they are thoroughly mixed and dispensed onto the facing.
• the MDI stream consisted of polymeric MDI.
• the compositions of the other three streams are indicated in Table II. The amounts are indicated in parts by weight (pbw) .
• the stream rates were:
• the properties of the open cell rigid foam-based laminate were:
• Thermal conductivity at 10 °C was determined by putting the laminate between two plates, one having a temperature of 0 °C and the other having a temperature of 20 °C, and determining the amount of heat transferred through the laminate from the warm plate to the cold plate per second per meter of laminate per degree Kelvin temperature difference.
• the laminate has a relatively low density and a low closed cell content, while at the same time exhibiting excellent mechanical stability and low thermal conductivity, thus making it very useful as an insulating material.

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• 1999
  • 1999-05-18 EP EP99926339A patent/EP1086158A1/de not_active Withdrawn
  • 1999-05-18 JP JP2000549662A patent/JP2002515527A/ja active Pending
  • 1999-05-18 AU AU43638/99A patent/AU4363899A/en not_active Abandoned
  • 1999-05-18 CA CA002329070A patent/CA2329070A1/en not_active Abandoned
  • 1999-05-18 WO PCT/EP1999/003453 patent/WO1999060045A1/en not_active Application Discontinuation

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