US20050027044A1 - Process of making press molded materials using heat activated tertiary amine urethane catalysts - Google Patents

Process of making press molded materials using heat activated tertiary amine urethane catalysts Download PDF

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US20050027044A1
US20050027044A1 US10/838,160 US83816004A US2005027044A1 US 20050027044 A1 US20050027044 A1 US 20050027044A1 US 83816004 A US83816004 A US 83816004A US 2005027044 A1 US2005027044 A1 US 2005027044A1
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tertiary amine
catalyst
diisocyanate
carboxylic acid
temperature
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Christopher Moriarty
Robert Grigsby
Robert Zimmerman
Sachchida Singh
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Huntsman Petrochemical LLC
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Huntsman Petrochemical LLC
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    • 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
    • C08G18/08—Processes
    • C08G18/16—Catalysts
    • C08G18/18—Catalysts containing secondary or tertiary amines or salts thereof
    • C08G18/1875—Catalysts containing secondary or tertiary amines or salts thereof containing ammonium salts or mixtures of secondary of tertiary amines and acids
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C217/00—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton
    • C07C217/02—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton
    • C07C217/04—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated
    • C07C217/06—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one etherified hydroxy group and one amino group bound to the carbon skeleton, which is not further substituted
    • C07C217/08—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one etherified hydroxy group and one amino group bound to the carbon skeleton, which is not further substituted the oxygen atom of the etherified hydroxy group being further bound to an acyclic carbon atom

Definitions

  • This invention pertains to a process for making press molded materials such as orientated strand boards using a heat activated urethane catalyst that are formed from a tertiary amine-carboxylic acid salt, where the carboxylic acid and tertiary amine are selected such that the compound unblocks at a given temperature.
  • Urethane is frequently polymerized through use of a catalyst such as a tertiary amine.
  • a catalyst such as a tertiary amine.
  • the inventors have recognized that a need exists for such a heat activated catalyst in the production of press molded materials such as orientated strand boards.
  • the present invention provides a solution to one or more of the disadvantages and deficiencies described above.
  • this invention is a process for the manufacture of a press molded material, comprising: applying such as by spraying diisocyanate, polyol, and a catalyst to a wood material, wherein the catalyst is a tertiary amine-carboxylic acid salt that is blocked at room temperature and becomes unblocked at an elevated temperature, and heating (for example while under pressure so as to form a press molded material) the resulting mixture to a temperature effective to unblock the salt to produce unblocked tertiary amine.
  • this invention is a method useful for the production of orientated strand boards, comprising: applying such as by spraying a urethane composition on wood chips, applying such as by spraying a tertiary amine:carboxylic acid salt catalyst on the wood chips, compressing the chips, heating the compressed chips so that at least a portion of the salt catalyst unblocks to thereby initiate polymerization of the urethane composition.
  • the urethane and salt may be sprayed separately or simultaneous in admixture.
  • this invention is a composite formed of wood chips and the polymerization product of a urethane composition and tertiary amine: carboxylic acid salt that unblocks at a temperature of at least 135° C.
  • This invention employs a heat activated urethane catalyst which comprises a tertiary amine-carboxylic acid salt.
  • This salt is blocked and inactive at room temperature, but becomes unblocked at an elevated temperature (it is heat activated).
  • unblocked it is meant that the tertiary amine becomes a free, neutral compound and is not present as a salt of the carboxylic acid.
  • elevated temperature it is meant, for example, a temperature above about 110° C., or above about 125° C., or above about 135° C., or higher.
  • the salt becomes unblocked at a temperature above 135° C.
  • the tertiary amine may be N,N-dimethylcyclohexylamine, pentamethyldiethlenetriamine, N,N-dimethyl-2(2-aminoethyoxy)ethanol, pentamehyldipropylenetriamine, tetramethyldipropylenetriamine, dimethylaminoethoxyethanol, N,N,N′-trimethylaminoethyl-ethanolamine, 2-(dimethylamino)-ethanol, or a combination thereof; the tertiary amine may be dimethylaminoethoxyethanol, N,N,N′-trimethylaminoethyl-ethanolamine, 2-(dimethylamino)-ethanol, or a combination thereof; the carboxylic acid may contain less than 30 carbons; the carboxylic acid may be oxalic acid, salicylic acid, or a combination thereof; the amine may be N,N-dimethyl-2-(2-aminoethoxy)
  • the heat activated catalyst may be prepared by reacting a tertiary amine with a carboxylic acid to form the tertiary amine-carboxylic acid salts.
  • a tertiary amine is reacted to form a tertiary amine:carboxylic acid salt, wherein the carboxylic acid and tertiary amine are selected such that the salt for example unblocks at a temperature above about 110° C., or above about 125° C., or above about 135° C., or higher.
  • carboxylic acid and tertiary amine are selected, and provided in amounts, such that the resulting salt unblocks at a temperature above about 110° C., or above about 125° C., or above about 135° C., or a given higher temperature.
  • the tertiary amine may be N,N-dimethylcyclohexylamine, pentamethyldiethlenetriamine, N,N-dimethyl-2(2-aminoethyoxy)ethanol, pentamehyldipropylenetriamine, tetramethyldipropylenetriamine, dimethylaminoethoxyethanol, N,N,N′-trimethylaminoethyl-ethanolamine, 2-(dimethylamino)-ethanol, or a combination thereof; the tertiary amine may be dimethylaminoethoxyethanol, N,N,N′-trimethylaminoethyl-ethanolamine, 2-(dimethylamino)-ethanol, or a combination thereof; the carboxylic acid may contain less than 30 carbons; the carboxylic acid may be oxalic acid, salicylic acid, or a combination thereof; the amine may be N,N-dimethyl-2-(2-aminoethoxy)ethanol
  • the heat activated catalyst may be used to make polyurethane by combining a diisocyanate, a polyol, and a catalyst, wherein the catalyst the catalyst is a tertiary amine-carboxylic acid salt that becomes unblocked above 135° C., and heating the resulting composition to unblock the salt to thereby polymerize the composition to form a polyurethane composition.
  • the tertiary amine may be N,N-dimethylcyclohexylamine, pentamethyldiethlenetriamine, N,N-dimethyl-2(2-aminoethyoxy)ethanol, pentamehyldipropylenetriamine, tetramethyldipropylenetriamine, dimethylaminoethoxyethanol, N,N,N′-trimethylaminoethyl-ethanolamine, 2-(dimethylamino)-ethanol, or a combination thereof; the tertiary amine may be dimethylaminoethoxyethanol, N,N,N′-trimethylaminoethyl-ethanolamine, 2-(dimethylamino)-ethanol, or a combination thereof; the carboxylic acid may contain less than 30 carbons; the carboxylic acid may be oxalic acid, salicylic acid, or a combination thereof; the amine may be N,N-dimethyl-2-(2-aminoeth
  • the tertiary amine-carboxylic acid salt of this invention is blocked and stable at room temperature and becomes unblocked.
  • the unblocking occurs generally at a temperature above about 110° C., or above about 125° C., or above about 135° C., or at higher given temperatures.
  • unblocking can be observed using Fourier transform infrared (FTIR) spectroscopy.
  • FTIR Fourier transform infrared
  • Unblocking is generally indicated by a carbonyl absorbance at 1730-1680 cm ⁇ 1 of at least 0.5 above 135° C., and in another embodiment at least 0.5 above 150° C.
  • the catalyst becomes active when it is unblocked, whereby polymerization of the urethane precursors commences.
  • the catalyst employed in the practice of this invention shows little or no activity at room temperature but becomes active at elevated temperature.
  • the activation temperature can be controlled by choice of the amine and carboxylic acid.
  • An additional surprising result is the 1:1 mole ratio of N,N-dimethyl-2-(2-aminoethoxy)ethanol:oxalic acid gave this property while the 2:1 mole ratio of these components did not.
  • N,N-dimethyl-2-(2-aminoethoxy)ethanol is available commercially under the name JEFFCAT ZR-70.
  • the mole ratio of tertiary amine to carboxylic acid is less than 2:1, in another embodiment is less than about 1.5, and in another embodiment is less than about 1.1.
  • the mole ratio of tertiary amine to carboxylic acid is from about 0.9:1 to about 1.1, and in another embodiment is about 1:1.
  • FIG. 1 shows the difference in isocyanate absorbances between a catalyzed, unblocked system and a non-catalyzed system as per example 2.
  • FIG. 2 shows the difference in carbonyl absorbances between a catalyzed, unblocked system and a non-catalyzed system as per example 2.
  • FIG. 3 shows the differences in isocyanate absorbances for catalysts A, C, F, G, no catalyst, and JEFFCATTM ZR-70 as per example 2.
  • FIG. 4 shows the difference in carbonyl absorbances for catalysts A, C, F, G, no catalyst, and JEFFCATTM ZR-70 as per example 2.
  • FIG. 5 shows the isocyanate absorbances for catalysts A, D, H, J, S, no catalyst, and JEFFCATTM ZR-70 as described in the examples.
  • FIG. 6 shows the carbonyl absorbances for catalysts A, D, H, J, S, no catalyst, and JEFFCATTM ZR-70 as described in the examples.
  • FIG. 7 shows the difference in isocyanate absorbances for catalysts prepared from 1:1 mole ratio versus a mole ratio of 2:1 of tertiary amine to carboxylic acid.
  • FIG. 8 shows the difference in carbonyl absorbances for catalysts prepared from 1:1 mole ratio versus a mole ratio of 2:1 of tertiary amine to carboxylic acid.
  • FIGS. 9 and 11 show the isocyanate absorbances for certain catalysts which did not unblock.
  • FIGS. 10 and 12 show the carbonyl absorbances for certain catalysts which did not unblock.
  • the tertiary amine-carboxylic acid salts of this invention can be prepared from a variety of starting compounds.
  • the salts are made by contacting a tertiary amine with a carboxylic acid, typically in an aqueous mixture.
  • the salts may be isolated and purified using standard techniques well known to one of skill in the art.
  • the salts are used as heat activated catalysts for urethanes.
  • the application of this technology in polyurethane involves heating a mixture of an isocyanate and some form of a hydroxyl type material in the presence of the blocked tertiary amine-carboxylic acid salt to a temperature such that the salt becomes unblocked, with the catalyst thereby becoming activated.
  • the temperature at which the catalyst becomes unblocked may vary depending on the specific amine/acid salt at issue.
  • the tertiary amines used in the practice of this invention are selected such that the tertiary amine selected in combination with a given carboxylic acid is blocked at room temperature and becomes unblocked at elevated temperature, such as above about 110° C. and in one embodiment above about 125° C., and in another embodiment above about 135° C.
  • the catalyst may provide a carbonyl absorbance at 1730-1680 cm ⁇ 1 of at least 0.5 above 135° C. as measured in admixture with polyurethane precursors such as described.
  • These tertiary amines may be referred to as effective tertiary amines, in the context of this invention.
  • Tertiary amines can be readily determined as to whether in combination with a given carboxylic acid the tertiary amine is an effective tertiary amine through routine experimentation, as by forming the salt, combining the salt with polyurethane precursors, exposing the resulting composition to heat and determining whether the catalyst salt becomes unblocked above a given temperature such as above about 135° C.
  • certain tertiary amines may work with a given carboxylic acid but not with other carboxylic acids.
  • the effective tertiary amines contain less than 30 carbon atoms, and are aliphatic amines which may optionally include additional functionality such as one or more ether and/or one or more alcohol groups.
  • tertiary amines include but are not limited to N,N-dimethylcyclohexylamine (which can be referred to as “DMCHA”), pentamethyldiethlenetriamine (which can be referred to as “PMDETA”), N,N-dimethyl-2(2-aminoethyoxy)ethanol (which can be referred to as “DMDGA”), pentamehyldipropylenetriamine (currently available commercially from Huntsman under the trade name ZR40), tetramethyldipropylenetriamine (currently available commercially from Huntsman under the trade name ZR-50B), dimethylaminoethoxyethanol, N,N,N′-trimethylaminoethyl-ethanolamine, 2-(dimethylamino)-ethanol, and combinations thereof.
  • the tertiary amine is dimethylaminoethoxyethanol, N,N,N′-trimethylaminoethyl-ethanolamine, 2-(dimethylamin
  • the carboxylic acids used in the practice of this invention are selected such that the carboxylic acid selected in combination with a given tertiary amine is blocked at room temperature and becomes unblocked at elevated temperature, such as above about 110° C., or above about 125° C., or above about 135° C., or higher, and may provide for example a carbonyl absorbance at 1730-1680 cm ⁇ 1 of at least 0.5 above 135° C.
  • These carboxylic acids may be referred to as effective carboxylic acids, in the context of this invention. As such, certain carboxylic acids may work with a given tertiary amine but not with other tertiary amines.
  • Carboxylic acids can be readily determined as to whether in combination with a given tertiary amine the carboxylic acid is an effective carboxylic acid through routine experimentation, as by forming the salt, combining the salt with polyurethane precursors, exposing the resulting composition to heat and determining whether the catalyst salt becomes unblocked above about 110° C., or above about 125° C., or above about 135° C., or higher.
  • the effective carboxylic acids contain less than 30 carbons, and may optionally include additional functionality such as one or more ether and/or one or more alcohol groups.
  • Representative examples of such carboxylic acids include but are not limited to oxalic acid, salicylic acid, and combinations thereof.
  • Polyurethane is a well known polymer which, in general, is made by reacting diisocyanate, polyol, and the catalyst.
  • a number of different kinds of polyurethanes can be produced depending on the nature of the polyol used and degree of cross-linking achieved, for example.
  • a suitable blowing agent should be included, such as water as is known in the art.
  • Polyurethane foams generally have a higher amount of cross-linking.
  • Aliphatic, cycloaliphatic, aromatic, and heterocyclic diisocyanates can be used as starting materials, which in general may contain up to about 20 carbon atoms.
  • diisocyanates include but are not limited to naphthalene bis (4-phenyl isocyanate), 4,4′-diphenylmethane diisocyanate, 1,3- and 1,4-phenylene diisocyanate, toluene 2,4- and 2,6-diisocyanate (TDI), diphenylmethane 2,4′- or 4,4′-diisocyanate (MDI), and mixtures and/or oligomers (prepolymers) thereof. If a prepolymer is employed, its molecular weight is typically about 300 to 2000. Such a prepolymer is typically made by reacting a polyol with an excess amount of diisocyanate.
  • the polyol can be any conventional or specialty polyol used in the polyurethane field. Typically, the polyol has two to eight hydroxyl groups. In one embodiment, the polyol has a molecular weight of from 400 to 10,000, in some instances from 600 to 5,000.
  • the polyols can include polyesters, polyethers, polythioethers, polyacetals, polycarbonates, and polyester amides containing two to eight hydroxyl groups, and in some instances two to four hydroxyl groups.
  • the diisocyanate and polyol are employed so as to provide a NCO/OH ratio of from 1.1:1 to 10:1, typically 1.5:1 to 5:1.
  • the polyurethane is made by first combining the polyurethane precursors (diisocyanate, polyol, catalyst, and any other additives such as a blowing agent if foam is desired).
  • the salt catalyst of this invention does not initiate polyurethane formation at room temperature.
  • the precursor composition is heated to unblock the salt, whereby the unblocked tertiary amine catalyst initiates polyurethane formation.
  • the polyurethane compositions according to the invention may be applied as one or more layers to substrates by known methods such as spraying, brush coating, immersion or flooding or by means of rollers or doctor applicators.
  • a substrate to be coated may be treated with suitable primers before the process according to the invention is carried out.
  • the process according to the invention is suitable for the formation of coatings on any substrates, e.g., metals, plastics, wood or glass.
  • the polyurethane compositions may also be used to form articles per se.
  • the amine/carboxylic acid salt of this invention can be used as a catalyst for polyurethane in the production of structural product based on wood materials.
  • a representative example of such a structural product is an orientated strand board (OSB), which may be described as an engineered, mat-formed panel product made of strands, flakes, or wafers sliced from wood logs that is bonded with a polyurethane binder under heat and pressure.
  • the wood materials that can be employed in the practice of this invention may vary widely. Representative examples of such wood materials include but are not limited to wood, bark, cork, bagasse, straw, flax, bamboo, alfa grass, rice husks, sisal, and coconut fibers.
  • the material may be present in the form of granules, chips, fibers, or flour.
  • the materials may have an intrinsic water content of 0 to 35 percent by weight, frequently from 5 to 25 percent by weight.
  • the wood material is typically mixed with the polyurethane precursors (i.e., the diisocyanate, polyol, and catalyst) so as to provide a final composition that contains from about 1 to about 50, more typically 1 to 15 percent by weight, of the polyurethane precursors.
  • the wood material is sprayed with these materials to effect mixing, as is known to one of skill in the art.
  • An advantage of this invention is that the catalyst has essentially no catalytic effect until heat activated above an elevated temperature such as above about 110° C., above about 125° C., or above about 135° C.
  • the polyurethane so formed serves as a binder for the wood material to hold the compress molded product together.
  • the catalyst When sprayed, the catalyst may be sprayed in admixture with water or one or more organic solvents.
  • organic solvents For example, ethylene carbonate, propylene carbonate, or mixtures thereof can be employed as a solvent so that application of the catalyst.
  • an organic solvent should not react with the diisocyanate or polyol, evaporate readily, and be compliant with environmental regulations for a given end use.
  • Additional representative classes of organic solvents that can be employed include but are not limited to aprotic organic solvents capable of solubilizing the components, such as esters including ethyl acetate, propyl acetate, and butyl acetate, ethers, hydrocarbons, ketones, amides, and so on.
  • suitable solvents include xylene, methyl isobutyl ketone, methoxypropyl acetate, N-methyl pyrrolidone, Solvesso solvent, petroleum hydrocarbons, iso-butanol, butyl glycol, chlorobenzenes and mixtures of such solvents.
  • the mixture of wood product and polymeric precursors are then typically compacted in a mold.
  • the compacted mixture is exposed to rapid heating so that at least a portion of the compacted mixture achieves a temperature above about 135° C., for example, often under pressure up to 3 atmospheres, though atmospheric and reduced pressure may also be used.
  • the temperature of the heat applied to the compacted material to be treated is typically up to 180° C. to 200° C., though higher and lower temperatures can be used.
  • a temperature gradient develops over the molded product, with temperatures above 135° C. in at least a portion of the product, thereby initiating unblocking of the salt and thus initiating curing of the polyurethane.
  • Other materials useful in the reaction may include surfactants, polyols, water, wood products, plastasizers, mold release agents, and flame retardants, as well as other common polyurethane additives.
  • an ultraviolet stabilizer can be employed in the practice of this invention.
  • Such ultraviolet stabilizers may include a sterically hindered piperidine derivative, such as an alkyl substituted hydroxy piperidine derivative.
  • the ultraviolet stabilizer includes the reaction product of an ester of a carboxylic acid and to alkyl substituted hydroxy piperidines.
  • the ultraviolet stabilizer is bis-(1, 2, 2, 6, 6-tetramethyl-4-piperidinyl) sebacate, known as TINUVINTM 765 and commercially available from Ciba-Geigy.
  • An UV absorber can be used in the instant invention, and may generally include a substituted benzotriazole, such as a phenyl substituted benzotriazole.
  • the UV stabilizer is a hydroxyl, alkyl substituted benzotriazole.
  • the UV stabilizer is 2-(2′-hydroxy-3′,5′-di-tert-amylphenyl)benzotriazole, known as TINUVINTM and commercially available from Ciba-Geigy.
  • An antioxidant may be used in the instant invention such as a substituted, sterically hindered phenol, such as a substituted ester of hydroxyhydrocinnamic acid.
  • the antioxidant element is a 3,5-dialkyl ester of hydroxyhydrocinnamic acid, and another embodiment is octadecyl 3,5-di-tert-butyl-4-hydroxyhydrocinnamate, known as IRGANOXTM 1076 and commercially available from Ciba-Geigy.
  • the amount of additive incorporated in the polyurethane depends on several factors, including the desired stability of the polyurethane, so the amount of additive can be adjusted according to the intended use of the polyurethane.
  • a useful amount of additive in the polyurethane can be an amount of up to about 5 percent by weight, and in one embodiment is in an amount of from about 0.5 to about 3 percent by weight.
  • Example 1 describes the synthesis of various acid blocked amine catalysts.
  • Example 2 illustrates the effectiveness of these derivatives over the control material.
  • the control material, catalyst G is the material described in U.S. Pat. No. 6,007,649.
  • the effect that these catalysts have on a PIR foam was determined by using a REACTFTIR 1000 instrument using a heated probe.
  • the heated probe was programmed to start at 70 C and hold at this temperature for 10 minutes. It was ramped up to 180 C over a thirty-minute period. At this point, it was held for 15 minutes at 180 C. Approximately 574 FTIR spectra were recorded during this time period from 800-4000 cm ⁇ 1 .
  • the formulation used to test these catalyst consisted of a pre-blend of RUBINATE 1840 (70 pbw), diisononylphthalate (20 pbw), and Tegostab B-8407, (7.0 pbw).
  • FIGS. show the effect that the catalysts have on either the isocyanate or carbonyl absorbance.
  • Isocyanate absorbance will decrease over time as the isocyanate is consumed.
  • Carbonyl absorbance will increase as the amount of carbonyl absorbing species increases in the reacting mixture.
  • the graph of the temperature profile is also shown in all of these graphs. The right side of each graph shows the temperature scale. Inspection of some of the these graphs will show that, at a certain temperature, either a sharp decrease in isocyanate absorbance, which translates to using up the isocyanate quicker, or a sharp rise in carbonyl absorbance, which translates to forming more carbonyl species.
  • These carbonyl species are either from the reaction of the isocyanate and water, isocyanate and polyol, or trimerization of the isocyanate into an isocyanurate material or any combination of these reactions.
  • FIGS. 1 and 2 shows the difference in isocyanate and carbonyl absorbance between a catalyzed (JEFFCAT ZR-70) or unblocked system and a non-catalyzed system.
  • the catalyzed system reacts quicker than the uncatalyzed system.
  • the catalyzed system is not blocked in any manner.
  • the isocyanate absorbance should closely follow the uncatalyzed system but should accelerate at some point and start consuming isocyanate.
  • FIG. 3 The following figures illustrate the improvement over the art, which uses JEFFCAT DMEA and malonic acid (catalyst G).
  • a delay is shown for this derivative but it never kicks in to accelerate the consumption of the isocyanate, FIG. 3 . It does slowly use up the isocyanate at a greater rate than the uncatalyzed system. It functions as a blocked catalyst but does not unblock at any particular temperature. There is a point where formation of the carbonyl species slowly increases, as shown in FIG. 4 .
  • FIGS. 3 and 4 An improvement is shown in FIGS. 3 and 4 by the delay of JEFFCAT DMEA and oxalic acid (catalyst C) and in particular at about 170° C. where this derivative starts to accelerate the consumption of the isocyanate and the formation of carbonyl species.
  • the higher carbonyl absorbance of the JEFFCAT DMEA and oxalic acid shows that a higher concentration of the carbonyl species is formed from this catalyst.
  • a further improvement of this invention is illustrated by the catalyst composed of JEFFCAT ZR-70 and oxalic acid (catalyst A).
  • Catalyst A the catalyst composed of JEFFCAT ZR-70 and oxalic acid
  • the temperature of the conversion of the isocyanate and formation of carbonyl species occurs at a lower temperature for JEFFCAT ZR-70 than JEFFCAT DMEA, that is, 150° C. versus 170° C.
  • the uniqueness of the salt of JEFFCAT ZR-70 and oxalic acid is further illustrated by observing the isocyanate and carbonyl absorbencies profiles of JEFFCAT ZR-70 and malonic acid (catalyst F) and compare it with the unblocked JEFFCAT ZR-70. They are practically identical. There is no delay for catalyst F like there is with catalyst A.
  • JEFFCAT Z-110 also shows the unusual effect of blocking and then unblocking when a certain temperature is reached. This is shown in FIGS. 5 and 6 .
  • the temperature at which the JEFFCAT Z-110+oxalic acid (catalyst D) becomes unblocked and starts to consume isocyanate at a faster rate is lower than the salt of JEFFCAT ZR-70 and oxalic acid (catalyst A).
  • the reaction of JEFFCAT ZR-70/oxalic acid was done in a 1/1 mole ratio (catalyst A) and a 2/1 mole ratio (catalyst B).
  • the 2/1 mole ratio was not as effective at blocking or delaying the isocyanate consumption or isocyanurate formation as the 1/1 salt, as seen FIGS. 7 and 8 .
  • the 2/1 mole ratio salt did not show any acceleration in isocyanate consumption as opposed to the 1/1 mole ratio salt, which did.
  • FIGS. 9-12 Other catalysts which did not show any signs of blocking and unblocking, and thus are comparative examples, are shown in FIGS. 9-12 . These examples further demonstrate the uniqueness of the catalysts of this invention.
  • Cure rates for various catalyzed and un-catalyzed p-MDI binders were determined using an automated bonding evaluation system (ABES).
  • ABES testing method enables the study of various adhesive and adherent variables.
  • small lap shear tests were performed under controlled conditions of temperature, pressing load, and pressing time. Immediately after each bond is partially cured to the required level, it is tested to destruction in shear mode. Tensile load and pulling head movement (sample elongation) are monitored digitally during the pulling, and strength (overlap area corrected peak shear load) is calculated.
  • bonds may be rapidly cooled after formation but before pulling.
  • the p-MDI binder was applied with a small paint brush to one side of the wood veneer samples having the following characteristics:
  • a test to determine the latency of the blocked catalyst of this invention was developed and run.
  • veneer samples were coated with the catalyzed binder and placed in a temperature and humidity controlled (38 degrees Centigrade, 45 percent relative humidity) cabinet for 30 minutes. These conditions simulate the dwell time that is required for blended flakes in a typical OSB manufacturing process.
  • the cure curve should remain similar to the catalyzed control cure curves.
  • the systems tested were: (1) p-MDI control, (2) p-MDI and catalyst D and soy oil, (3) p-MDI and soy oil, (4) p-MDI and soy oil and catalyst D.
  • the load measured in Newtons was measured at 20, 40, 60, and 150 seconds.
  • Southern Yellow Pine wood flakes obtained from a commercial OSB mill were spray atomized blended with p-MDI and catalyst in a rotary blender.
  • the p-MDI and catalyst 1% catalyst solids dilution in water or soy oil
  • the pressing cycles were 6 and 12 seconds/mm thickness to compare under-cured panels (6 sec/mm) to fully cured panels (11 sec/mm).
  • the panels were removed from the press and the thickness was measured to determine the degree of cure based on thickness spring back. A decrease in thickness indicates improved cure.
  • the OSB boards made with three catalyst D systems showed improved cure, especially at 6 seconds.
  • the control thickness was about 0.77 mm and the control with soy oil was about 0.8 mm.
  • the sample using soy/catalyst D was about 0.767 mm
  • the sample using water/catalyst D was about 0.76
  • the sample using water/catalyst D and aged was about 0.737. After 12 seconds, the differences of thicknesses between samples were not as significant.

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  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Polyurethanes Or Polyureas (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Catalysts (AREA)
  • Dry Formation Of Fiberboard And The Like (AREA)
US10/838,160 2003-05-01 2004-05-03 Process of making press molded materials using heat activated tertiary amine urethane catalysts Abandoned US20050027044A1 (en)

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US46699003P 2003-05-01 2003-05-01
US10/838,160 US20050027044A1 (en) 2003-05-01 2004-05-03 Process of making press molded materials using heat activated tertiary amine urethane catalysts

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US10/838,160 Abandoned US20050027044A1 (en) 2003-05-01 2004-05-03 Process of making press molded materials using heat activated tertiary amine urethane catalysts
US12/022,697 Expired - Lifetime US7579426B2 (en) 2003-05-01 2008-01-30 Heat activated tertiary amine urethane catalysts

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US (3) US7351859B2 (fr)
EP (2) EP1622856A4 (fr)
CN (2) CN100351281C (fr)
AU (2) AU2004236742A1 (fr)
CA (2) CA2524260A1 (fr)
NZ (1) NZ543377A (fr)
RU (2) RU2005137318A (fr)
WO (2) WO2004099280A2 (fr)

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US20070131862A1 (en) * 2005-12-13 2007-06-14 Huber Engineered Woods L.L.C. Method using NIR spectroscopy to monitor components of engineered wood products
US20070222100A1 (en) * 2006-03-21 2007-09-27 Huber Engineered Woods L.L.C. Method and system using NIR spectroscopy for in-line monitoring and controlling content in continuous production of engineered wood products
US20080167437A1 (en) * 2003-05-01 2008-07-10 Huntsman Petrochemical Corporation Heat Activated Tertiary Amine Urethane Catalysts
WO2008128036A1 (fr) * 2007-04-11 2008-10-23 Huber Engineered Woods Llc Procédé de traitement de toile et de formation de substrat en ligne pour des produits superposés
US20100168287A1 (en) * 2007-05-23 2010-07-01 Huntsman International Llc Adhesives, Reaction Systems, and Processes for Production of Lignocellulosic Composites

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PL2106415T3 (pl) * 2007-01-19 2016-10-31 Trzeciorzędowe aminy zablokowane kwasami polimerowymi
KR20140004091A (ko) * 2010-10-29 2014-01-10 루브리졸 어드밴스드 머티어리얼스, 인코포레이티드 수성의 양이온성 폴리우레탄 분산물
US9968919B2 (en) 2011-06-29 2018-05-15 Evonik Degussa Gmbh Reducing emissions in polyurethane foam
CN104603171B (zh) * 2012-06-29 2017-05-31 东曹株式会社 用于制造聚氨酯树脂的催化剂组合物及使用其的聚氨酯树脂的制造方法
US10393912B2 (en) * 2015-07-02 2019-08-27 Weatherford Technology Holdings, Llc Method of and apparatus for inverting three-dimensional fluid property distribution over the (T1,T2,D)domain from NMR measurements
CN108948317A (zh) * 2018-06-19 2018-12-07 旭川化学（昆山）有限公司 一种制造聚氨酯鞋底过程中可快速脱模的组合料
ES2837489B2 (es) * 2019-12-31 2022-02-28 Primalchit Solutions S L Mezcla de componentes organicos no polimericos con capacidad retardante de llama, metodo de preparacion y uso

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US3239480A (en) * 1962-02-03 1966-03-08 Bayer Ag Polyurethanes synthesized with the aid of carboxylic acid salts
US3980594A (en) * 1975-04-23 1976-09-14 The General Tire & Rubber Company Trimerization of aromatic isocyanates catalyzed by certain ammonium salts
US4464488A (en) * 1983-08-11 1984-08-07 Texaco Inc. Polyurethanes using monocarboxylic acid salts of bis(aminoethyl)ether derivatives as catalysts
US4521545A (en) * 1983-08-09 1985-06-04 Bayer Aktiengesellschaft Latent catalysts for the isocyanate polyaddition reaction
US4608407A (en) * 1983-08-09 1986-08-26 Bayer Aktiengesellschaft Process for the production of compression-molded materials containing polyisocyanate binders using latent, heat activatable catalysts
US4617286A (en) * 1983-09-08 1986-10-14 Toyo Soda Manufacturing Co., Ltd. Catalyst for polyurethane having delay property
US6007649A (en) * 1996-01-31 1999-12-28 Bayer Aktiengesellschaft Method of producing press-moulding materials with polyisocyanate binders and using latent, heat-activable catalysts
US6387972B1 (en) * 2001-02-15 2002-05-14 Crompton Corporation Process to enhance polyurethane foam performance
US6800667B1 (en) * 1998-08-21 2004-10-05 Basf Corporation Mixture containing isocyanates as well as organic and/or inorganic acid anhydrides
US7351859B2 (en) * 2003-05-01 2008-04-01 Huntsman Petrochemical Corporation Heat activated tertiary amine urethane catalysts

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US4186255A (en) * 1978-03-13 1980-01-29 Texaco Development Corporation Bis-quaternary ammonium salts as polyisocyanurate catalysts
DE2854384A1 (de) * 1978-12-16 1980-07-03 Bayer Ag Verfahren zur herstellung von polyurethan-kunststoffen
US4490517A (en) * 1983-10-03 1984-12-25 Olin Corporation Solid TDI residue-dicarboxylic ester binder composition and lignocellulosic composite materials prepared therefrom
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US2932621A (en) * 1956-02-07 1960-04-12 Pittsburgh Plate Glass Co Preparation of polyurethane foam utilizing a salt of dimethylethanol amine and a dicarboxylic acid as a catalyst
US3239480A (en) * 1962-02-03 1966-03-08 Bayer Ag Polyurethanes synthesized with the aid of carboxylic acid salts
US3980594A (en) * 1975-04-23 1976-09-14 The General Tire & Rubber Company Trimerization of aromatic isocyanates catalyzed by certain ammonium salts
US4521545A (en) * 1983-08-09 1985-06-04 Bayer Aktiengesellschaft Latent catalysts for the isocyanate polyaddition reaction
US4608407A (en) * 1983-08-09 1986-08-26 Bayer Aktiengesellschaft Process for the production of compression-molded materials containing polyisocyanate binders using latent, heat activatable catalysts
US4464488A (en) * 1983-08-11 1984-08-07 Texaco Inc. Polyurethanes using monocarboxylic acid salts of bis(aminoethyl)ether derivatives as catalysts
US4617286A (en) * 1983-09-08 1986-10-14 Toyo Soda Manufacturing Co., Ltd. Catalyst for polyurethane having delay property
US6007649A (en) * 1996-01-31 1999-12-28 Bayer Aktiengesellschaft Method of producing press-moulding materials with polyisocyanate binders and using latent, heat-activable catalysts
US6800667B1 (en) * 1998-08-21 2004-10-05 Basf Corporation Mixture containing isocyanates as well as organic and/or inorganic acid anhydrides
US6387972B1 (en) * 2001-02-15 2002-05-14 Crompton Corporation Process to enhance polyurethane foam performance
US7351859B2 (en) * 2003-05-01 2008-04-01 Huntsman Petrochemical Corporation Heat activated tertiary amine urethane catalysts

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20080167437A1 (en) * 2003-05-01 2008-07-10 Huntsman Petrochemical Corporation Heat Activated Tertiary Amine Urethane Catalysts
US7579426B2 (en) 2003-05-01 2009-08-25 Huntsman Petrochemical Corporation Heat activated tertiary amine urethane catalysts
US20070131862A1 (en) * 2005-12-13 2007-06-14 Huber Engineered Woods L.L.C. Method using NIR spectroscopy to monitor components of engineered wood products
US7279684B2 (en) 2005-12-13 2007-10-09 Huber Engineered Woods Llc Method using NIR spectroscopy to monitor components of engineered wood products
US20070222100A1 (en) * 2006-03-21 2007-09-27 Huber Engineered Woods L.L.C. Method and system using NIR spectroscopy for in-line monitoring and controlling content in continuous production of engineered wood products
WO2008128036A1 (fr) * 2007-04-11 2008-10-23 Huber Engineered Woods Llc Procédé de traitement de toile et de formation de substrat en ligne pour des produits superposés
US20100168287A1 (en) * 2007-05-23 2010-07-01 Huntsman International Llc Adhesives, Reaction Systems, and Processes for Production of Lignocellulosic Composites
US9314947B2 (en) * 2007-05-23 2016-04-19 Huntsman International Llc Adhesives, reaction systems, and processes for production of lignocellulosic composites

Also Published As

Publication number Publication date
CN1795162A (zh) 2006-06-28
EP1622959A2 (fr) 2006-02-08
AU2004236741A1 (en) 2004-11-18
WO2004099279A8 (fr) 2005-07-21
CN100406424C (zh) 2008-07-30
WO2004099279A2 (fr) 2004-11-18
AU2004236742A1 (en) 2004-11-18
WO2004099279A3 (fr) 2005-03-24
RU2005137315A (ru) 2006-06-10
NZ543377A (en) 2007-07-27
US7351859B2 (en) 2008-04-01
EP1622856A2 (fr) 2006-02-08
US20080167437A1 (en) 2008-07-10
US7579426B2 (en) 2009-08-25
CA2524267A1 (fr) 2004-11-18
RU2005137318A (ru) 2006-05-10
EP1622856A4 (fr) 2008-08-27
WO2004099280A2 (fr) 2004-11-18
CA2524260A1 (fr) 2004-11-18
WO2004099280A3 (fr) 2004-12-09
CN100351281C (zh) 2007-11-28
US20050027002A1 (en) 2005-02-03
CN1795220A (zh) 2006-06-28

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