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
  • C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
  • C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
  • C08G65/26—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other 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
  • 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
• • 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
  • C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
  • C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
  • C08G65/26—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds
  • C08G65/2603—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds the other compounds containing oxygen
  • C08G65/2606—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds the other compounds containing oxygen containing hydroxyl 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
  • C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
  • C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
  • C08G65/26—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds
  • C08G65/2642—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds characterised by the catalyst used
  • C08G65/2669—Non-metals or compounds thereof
  • C08G65/2672—Nitrogen or compounds thereof
• • 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
  • C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
  • C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
  • C08G65/26—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds
  • C08G65/2696—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds characterised by the process or apparatus used
• • 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

Definitions

• This invention relates to a process for preparing polyether polyols.
• This invention particularly relates to a process for preparing polyether polyols which are useful for preparing rigid polyurethane foams.
• Polyether polyols are useful for preparing polyurethane products . It is known to use polyether polyols in processes for preparing polyurethane products such as flexible foam, rigid foam, elastomers and sealants. Of these, rigid polyurethane foams are an important product having both insulative and structural uses.
• U.S. Patent No. 4,332,936 to Nodelman discloses preparing polyether polyols which are described as being particularly suitable for the production of rigid polyurethane foams. Therein, it is disclosed to mix or dissolve a multifunctional hydroxy initiator, such as sucrose, with dimethylformamide prior to reacting the initiator with an alkylene oxide in the presence of an amine catalyst.
• a multifunctional hydroxy initiator such as sucrose
• the present invention is a process for preparing a polyether polyol comprising admixing an initiator with an alkylene oxide in the presence of an imidazole catalyst under high temperature alkoxylation conditions sufficient to prepare a rigid polyether polyol with the proviso that when an aromatic amine initiator is used, alkoxylation is done at a temperature greater than 125°C.
• the present invention is a polyether polyol prepared by a process comprising admixing an initiator with an alkylene oxide in the presence of an imidazole catalyst under high temperature alkoxylation conditions sufficient to prepare a rigid polyether polyol with the proviso that when an aromatic amine initiator is used, alkoxylation is done at a temperature greater than 125°C.
• the present invention is a process for preparing rigid polyether polyols in the presence of an imidazole catalyst.
• an imidazole catalyst is any compound having the general formula:
• N 3 3 2C ⁇ /
• X, Y, Z, and Z' are hydrogen, methyl groups, ethyl groups, or phenyl groups in combination to include: imidazole, N-methylimidazole, 2-methylimidazole, 4-methylimidazole, 2-ethylimidazole, 2-ethyl-4- methylimidazole, N-phenylimidazole, 2-phenylimidazole, and 4-phenyl- imidazole. Combinations of these compounds can be used and are also referred to herein as imidazole catalysts.
• a polyol is prepared by admixing an initiator with an alkylene oxide in the presence of an imidazole catalyst.
• Initiators are starting materials useful for preparing polyols characterized in that they include at least 2 active hydrogen containing groups.
• an active hydrogen containing group is any group having a hydrogen which can react with an alkylene oxide in the presence of an imidazole catalyst.
• the active hydrogen containing group is an amino or hydroxy group.
• the active hydrogen containing group can be on an aliphatic or aromatic molecule.
• the initiators useful with the process of the present invention can be an
• the initiators useful with the process of the present invention can be an aromatic diamine or polyamine.
• Initiators useful with the present invention include water, organic dicarboxylic acids, such as succinic acid, adipic acid, phthalic acid and terephthalic acid, aliphatic and aromatic, unsubstituted or N-mono-, N,N- and N, N' -dialkyl-substituted diamines having from 1 to 4 carbon atoms in the alkyl moiety, such as unsubstituted or mono- or dialkyl-substituted ethylenediamine, diethylenetriamine, triethylenetetramine, 1, 3-propylenediamine, 1,3- and 1, 4-butylenediamine, 1,2-, 1,3-, 1,4-, 1,5- and 1, 6-hexamethylenediamine, phenylenediamines, 2,3-, 2,4- and 2,6- tolylenediamine and 4,4'- 2,4'- and 2, 2 ' -diaminodiphenylmethane .
• alkanolamines for example, ethanolamine, N-methyl- and N- ethyl-ethanolamine
• dialkanolamines for example, diethanolamine, N- methyl- and N-ethyl-diethanolamine
• trialkanolamines for example, triethanolamine, and ammonia.
• initiators used with the present invention are the polyhydric alcohols, in particular dihydric and/or trihydric alcohols, such as ethanediol, nonyl phenol, bisphenol-A, bisphenol-F, novolak phenolic resins, mannich base polyols derived from phenol or alkyl phenol reacted with formaldehyde and diethanol or dipropanolamine (mannich bases), propylene glycol, dipropylene glycol, 1, 4-butanediol, 1, 6-hexanediol, glycerol, trimethylolpropane, pentaerythritol, sorbitol, alpha methyl glucoside and sucrose.
• water is a dihydric alcohol because the reaction product of water and an alkoxide is a dihydric alcohol.
• the initiators used with present invention are glycerine, water, sucrose and mixtures thereof.
• Initiators useful with the present invention can also be alkoxylation products of the above listed initiator molecules.
• an initiator useful with the present invention is a propoxylated or ethoxylated ethylene glycol.
• Another example of a similar useful initiator is a propoxylated or ethoxylated glycerin.
• Still another example of a similar useful initiator is a propoxylated or ethoxylated propylene glycol.
• initiators can be used with the present invention and are also preferred.
• mixed initiators include mixtures such as: sucrose and water; glycerin and sorbitol; propylene glycol and sucrose; and ethylene glycol and sucrose. More preferably, the initiators used with the present invention are propoxylated mixed initiators. Most preferably, the initiator used with the present invention is a propoxylated mixture of sucrose and glycerin.
• a polyol is prepared by admixing an initiator with an alkylene oxide in the presence of an imidazole catalyst.
• the alkylene oxides which can be used with the present invention include any which are useful in preparing polyether polyols.
• the alkylene oxide has from 2 to 8 carbons. More preferably, the alkylene oxide has from 2 to 4 carbons.
• the alkylene oxide is ethylene oxide, propylene oxide, butylene oxide and mixtures thereof.
• the polyols prepared by the process of the present invention can be used in any application where a similar conventional polyol could be used, but are particularly useful in preparing rigid polyurethane foams.
• Polyols useful for preparing rigid polyurethane foams typically have: an OH functionality of from 2 to 8; an OH number of from 200 to 2000; and a molecular weight of from 62 to 2000. These ranges represent the typical reaction products resulting from the alkoxylation of initiators such as water which has a low OH functionality of 2 and initiators such as sucrose which has a high OH functionality of 8.
• the present invention also contemplates the alkoxylation of initiators having intermediate functionalities as well as mixtures of initiators.
• the polyols of the present invention have an average functionality of from 2 to 8, an OH number of from 200 to 800, and a molecular weight of from 150 to 2,400. More preferably, the polyols of the present invention have an average functionality of from 3 to 8, an OH number of from 200 to 600, and a molecular weight of from 300 to 2,400. Most preferably, the polyols of the present invention have an average functionality of from 4 to 8, an OH number of from 300 to 600, and a molecular weight of from 350 to 1,600.
• catalyst Preferably, from 0.0001 parts to 0.01 parts of imidazole catalyst are used. Most preferably 0.001 parts of an imidazole catalyst are used. Parts of catalyst are calculated by dividing the weight of imidazole catalyst used by the total weight of product made and diluent present in the reactor.
• the reaction of an initiator and an alkylene oxide are done in the process of the present invention under high temperature alkoxylation conditions sufficient to prepare a polyether polyol.
• the art of preparing conventional polyether polyols by conventional processes is well known to those of ordinary skill in the art of preparing polyols.
• the high temperature alkoxylation conditions of the present invention substantially the same except the temperatures at which the alkoxylation are done is at from 100°C to near but not at the decomposition or discoloration point of the polyol. These conditions include a pressure of from 10 psig (69 kPa) to 100 psig (690 kPa) and a temperature of from 100°C to 150°C.
• the high temperature alkoxylation conditions are a pressure of from 30 psig (206 kPa) to 80 psig (551 kPa) . Even more preferably, the temperature of the high temperature alkoxylation conditions is from 120°C to 150°C. Most preferably, the temperature of the high temperature alkoxylation conditions is from 130°C to 145°C. When the process of the present invention is used to prepare polyols from formulations including aromatic amine initiators, the alkoxylation is done at a temperature of greater than 125°C.
• An advantage of the imidazole catalysts used with the process of the present invention when they are compared with other conventional amine catalysts such as triethylamine, trimethylamine and methyldiethylamine is that the imidazole catalysts have both a high level of reactivity at conventional alkoxylation temperatures and the reactivity of imidazole catalysts increases with temperature up to the decomposition point for most polyols and initiators. For example, trialkyla ine catalysts begin to lose catalytic activity as alkoxylation temperature is increased starting at about 110°C while the imidazole catalysts continue to increase in catalytic activity until the reaction temperature reaches at least 150°C.
• Suitable diluents include any polyether or polyester polyol which was prepared such that at least two and preferably three alkylene oxides were added to each active hydrogen of the initiator.
• polyols wherein more than 2 alkylene oxide groups have been added can be used as diluents without the polyol reacting further with alkylene oxides.
• This can be an advantage, particularly when alkoxylating solid initiators such as sucrose and sorbitol.
• This is particularly an advantage when it is desired to prepare a substantially homogenous polyol prepared from solid initiators because a polyol which is substantially similar to the desired product polyol can be used as a solvent for the initiator.
• Polyols are often prepared by both continuos and batch processes.
• a polyol is made by charging the components of a formulation in one or more steps, but essentially all of any given component is charged at one time.
• all of the initiator for the polyol is placed into a reactor at the start of the reaction. That "batch" of raw materials is then taken through the steps of making the polyol to produce a single "batch" of polyols.
• a continuos process the raw materials are fed into a production unit continuously, so that the polyol is at different stages of production at different points in the production unit.
• the imidazole catalysts of the present invention can be used with either batch or continuos processes.
• polyols prepared by the process of the present invention can be used in the same way as are similar conventional polyols prepared using conventional processes.
• the polyols of the present invention can be used as prepared or admixed with additives .
• the polyols of the present invention can be admixed with other types of polyols.
• Example 1 A mixture of 300g of glycerin and 0.5g of 2-ethyl-4- methylimidazole was heated to 100°C in a 1 liter pressure vessel equipped with a stirrer. After the vessel reaches thermal equilibrium, 11.96g of propylene oxide were injected into the vessel. The initial concentration of propylene oxide was measured by gas chromatography to be 1.8 percent. After 195 minutes, the concentration of propylene oxide was 0.04 percent.
• Example 2 A mixture of 10.6 pounds (4.8Kg) of VORANOL 490* and 7.1 pounds (3.2Kg) of VORANOL 370** was added to a 20 gallon (75.7L) pressure vessel. To this were added 0.1 pounds 45.4g) of 2-ethyl-4- methylimidazole and 16 pounds (7.3Kg) of sucrose. The admixture was heated and stirred under a nitrogen pad until it reaches thermal equilibrium at 120°C. Next, 43 (19.5Kg) pounds of propylene oxide were added at a rate of 0.11 pounds (49.9g) per minute and then the admixture was maintained at 120°C for five hours.
• the final product was analyzed for physical properties and has a viscosity of 78.7Cs at 210°F (98.8°C), a hydroxyl content of 10.73 percent, and a Gardener color of 13.
• VORANOL 490 is a trade designation of The Dow Chemical Company.
• **VORANOL 370 is a trade designation of The Dow Chemical Company.
• Example 3 A series of experiments was run where l-methoxy-2-propanol was reacted with propylene oxide using trimethylamine and 2-ethyl-4- methylimidazole as catalysts. The reactions were run in a 1 liter, stirred stainless steel pressure vessel that was heated with electrical coil heaters to maintain temperature control. The vessel was loaded with about 300 grams of l-methoxy-2-propanol, closed and then purged with nitrogen to remove oxygen. For the runs using trimethylamine as a catalyst, 300 ml of gaseous trimethylamine catalyst was added as a gas using a 50 ml syringe.
• the rate of the reaction was followed by plotting the unreacted PO concentration versus time.
• a second order rate constant may be derived by division of this slope by the molar base concentration.
• the Table below lists the rate data for these reactions.
• Reaction rates for propoxylation vary with amine catalyst and polyol reactant . Low equivalent weight alcohols or polyols react faster than materials already propoxylated. It can be seen that the rate of propoxylation decreases with reaction temperature for trimethylamine and increases for imidazoles.
• Suc-glyc is a polyether polyol based on 60/40 weight ratio of sucrose/glycerine propoxylated to an OH number of 370
• the titration analysis of the catalyst was done by adding about 5 g of sample to 50 ml methanol. This was titrated using a Mettler DL40 autotitrator (Mettler DL40 is a trade designation of the Mettler Company) . The total basicity was taken as the sum of all endpoints in the titration.
• Example 4 A polyol based on a 60/40, by weight, mixture of sucrose/glycerine, propoxylated to an equivalent hydroxyl weight of about 150 (specification range 10.8-11.6% OH, viscosity 0.89 - 1.17 poise (0.089 - 0.117 Ns/m 2 ) wass used as a reaction solvent. 468 grams of this polyol was admixed with 419 grams of sucrose and 1.82 grams of N-methylimidazole. This admixture was stirred in a 4 liter pressure vessel which was heated to 130°C and maintained at 130 ⁇ 0.5°C for the course of the reaction. 1113 grams of propylene oxide was added using a positive displacement pump over 4.1 hours.
• the amount of residual propylene oxide was measured by monitoring the reactor pressure over the final 2 hr period. A rate constant was obtained by plotting the natural log of pressure against time until the pressure remains constant. The slope of this plot gives a linear first order plot with a slope of -0.0756 per minute. Division of this value by the catalyst concentration at the end of reaction (measured as 1040 ppm or 0.0127 milliequivalents/g) gives a second order rate constant of 5.95 g/meq.-min. The resulting product had 12.16% OH and a viscosity of 1.05 poise (0.105 Ns/m 2 ) at 210°F (98.9°C).

Landscapes

• Chemical & Material Sciences (AREA)
• Health & Medical Sciences (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Medicinal Chemistry (AREA)
• Polymers & Plastics (AREA)
• Organic Chemistry (AREA)
• Polyurethanes Or Polyureas (AREA)
• Polyethers (AREA)

Applications Claiming Priority (3)

Publications (1)

Family

ID=22061855

Family Applications (1)

Country Status (14)

Families Citing this family (19)

Family Cites Families (3)

• 1998
  • 1998-11-12 AR ARP980105741A patent/AR017610A1/es unknown
  • 1998-11-13 CN CN98811124A patent/CN1278838A/zh active Pending
  • 1998-11-13 KR KR1020007005178A patent/KR20010015813A/ko not_active Application Discontinuation
  • 1998-11-13 TR TR2000/01289T patent/TR200001289T2/xx unknown
  • 1998-11-13 CO CO98067228A patent/CO5050318A1/es unknown
  • 1998-11-13 EP EP98967113A patent/EP1037936A1/en not_active Withdrawn
  • 1998-11-13 PL PL98340826A patent/PL340826A1/xx unknown
  • 1998-11-13 JP JP2000536770A patent/JP2002506897A/ja active Pending
  • 1998-11-13 CA CA002309138A patent/CA2309138A1/en not_active Abandoned
  • 1998-11-13 BR BR9813280-6A patent/BR9813280A/pt not_active Application Discontinuation
  • 1998-11-13 ZA ZA9810410A patent/ZA9810410B/xx unknown
  • 1998-11-13 WO PCT/US1998/024332 patent/WO1999047581A1/en not_active Application Discontinuation
  • 1998-11-13 AU AU52641/99A patent/AU5264199A/en not_active Abandoned
  • 1998-11-13 ID IDW20000776A patent/ID24600A/id unknown

Non-Patent Citations (1)

Also Published As

Similar Documents

Legal Events