C08G18/82

METHOD FOR RECOVERING RAW MATERIALS FROM POLYURETHANE PRODUCTS

The invention relates to a method for recovering raw materials from polyurethane products, having the steps of: (A) providing a polyurethane product based on an isocyanate component and a polyol component; (B) reacting the polyurethane product with an alcohol in the presence of a catalyst, wherein a first product mixture containing alcohol, polyols, carbamates, and optionally water is obtained; (C) preparing the first product mixture, having the steps of: (C.I.) mixing the first product mixture obtained in step (B) with an organic solvent, which can be mixed with the alcohol used in step (B), optionally followed by a separation of solid components, thereby obtaining a second product mixture; (C.II) washing the second product mixture obtained in step (C.I) using an aqueous washing fluid, wherein carbamates contained in the second product mixture are hydrogenated partly while releasing amines and alcohol, and carrying out a phase separation into a first solvent phase, containing the organic solvent used in step (C.I) and polyols, and a first aqueous phase, containing water, alcohol, carbamates, and amines; and (C.III) processing the first solvent phase, thereby obtaining the polyols; and optionally (D) processing the first aqueous phase, thereby obtaining an amine which corresponds to an isocyanate of the isocyanate component.

METHOD FOR RECOVERING RAW MATERIALS FROM POLYURETHANE PRODUCTS

The invention relates to a method for recovering raw materials from polyurethane products, having the steps of: (A) providing a polyurethane product based on an isocyanate component and a polyol component; (B) reacting the polyurethane product with an alcohol in the presence of a catalyst, wherein a first product mixture containing alcohol, polyols, carbamates, and optionally water is obtained; (C) preparing the first product mixture, having the steps of: (C.I.) mixing the first product mixture obtained in step (B) with an organic solvent, which can be mixed with the alcohol used in step (B), optionally followed by a separation of solid components, thereby obtaining a second product mixture; (C.II) washing the second product mixture obtained in step (C.I) using an aqueous washing fluid, wherein carbamates contained in the second product mixture are hydrogenated partly while releasing amines and alcohol, and carrying out a phase separation into a first solvent phase, containing the organic solvent used in step (C.I) and polyols, and a first aqueous phase, containing water, alcohol, carbamates, and amines; and (C.III) processing the first solvent phase, thereby obtaining the polyols; and optionally (D) processing the first aqueous phase, thereby obtaining an amine which corresponds to an isocyanate of the isocyanate component.

Value Chain Return Process for Spent Polyurethanes by Hydrogenation

Spent polyurethanes are returned to the value chain by hydrogenating the spent polyurethanes in a hydrogen atmosphere in the presence of at least one homogeneous transition metal catalyst complex, wherein the transition metal is selected from metals of groups 7, 8, 9 and 10 of the periodic table of elements according to IUPAC, to obtain a polyamine and a polyol. The hydrogenation is carried out at a reaction temperature of at least 120° C. in a non-reducible solvent having a dipole moment of 10-10.sup.30 C.Math.m or less.

Value Chain Return Process for Spent Polyurethanes by Hydrogenation

Spent polyurethanes are returned to the value chain by hydrogenating the spent polyurethanes in a hydrogen atmosphere in the presence of at least one homogeneous transition metal catalyst complex, wherein the transition metal is selected from metals of groups 7, 8, 9 and 10 of the periodic table of elements according to IUPAC, to obtain a polyamine and a polyol. The hydrogenation is carried out at a reaction temperature of at least 120° C. in a non-reducible solvent having a dipole moment of 10-10.sup.30 C.Math.m or less.

Polymeric radiation-sources

A polymeric radiation-source with customized geometries to maximize receipt of radiation into treatment areas that is formed from either radioisotopes molecularly bonded to a polymer or radioisotopes encased within a polymer.

Polymeric radiation-sources

A polymeric radiation-source with customized geometries to maximize receipt of radiation into treatment areas that is formed from either radioisotopes molecularly bonded to a polymer or radioisotopes encased within a polymer.

IMPROVED DISTILLATION CAPABILITY BY DILUTION WITH A COMPONENT TO BE SEPARATED OFF

The invention relates to a method for purifying at least one reaction product of at least one diisocyanate, comprising at least the following steps: (A) providing a mixture A at least containing the at least one reaction product of the at least one diisocyanate and, if applicable, the at least one diisocyanate, (B) adding, if applicable more of, at lease one diisocyanate to mixture A from step (A) in order to obtain a mixture B, and (C) separating off the at least one diisocyanate from mixture B from step (B) by distillation in order to obtain the purified at least one reaction product of the at least one diisocyanate. Furthermore, the present invention comprises the reaction product of at least one diisocyanate which can be obtained by the method according to the invention and the use thereof for producing polyurethane foams, polyurethane hydrogels, polyurethane elastomers, varnishes and bonding adhesives.

METHOD FOR RECOVERING RAW MATERIALS FROM POLYURETHANE PRODUCTS

The invention relates to a method for recovering raw materials from polyurethane products, comprising the steps of (A) providing a polyurethane product that is based on an isocyanate component and a polyol component; (B) reacting the polyurethane product with a (mono- or polyvalent) alcohol in the presence of a catalyst, thereby obtaining a first product mixture; (C) obtaining the polyols from the first product mixture, comprising (C.I) mixing, without prior removal of any water that might be contained in the first product mixture, the first product mixture obtained in step (B) with an organic solvent that is not completely miscible with the alcohol used in step (B), and phase separation into a first alcohol phase and a first solvent phase; (C.II) processing the first solvent phase and obtaining polyols; and preferably (D) obtaining amines.

DEGRADABLE POLYMERS AND MONOMERS THEREFOR

Hydroxyacetal or hydroxyketal monomers, processes for their preparation, their use to produce degradable polymers, hydroxy-functional intermediates resulting from degradation, and repurposed polymers made from the hydroxy-functional intermediates are described. The invention avoids the energy-intensive conditions normally used to degrade polyurethanes and generates new hydroxy-functional intermediates that can be repurposed or upcycled. Polyurethanes and melamines, materials once destined for a landfill, can have a second life. Incorporation of a photoacid generator into microcapsule core materials and fabrication of the shell from the hydroxy-functional acetal or ketal monomers promotes facile, inside-out, solid-state degradation of the microcapsule shell triggered by UV light and acid generation in a hydrophobic environment. This enables controlled release of flavors, fragrances, biocides, agricultural actives, or other oil-based beneficial agents from within the microcapsules.

MODIFICATION METHOD OF POLYURETHANE, POLYURETHANE, POLISHING PAD, AND MODIFICATION METHOD OF POLISHING PAD

A modification method of a polyurethane, including the steps of: preparing a polyurethane having an ethylenically unsaturated bond; and treating the polyurethane with a liquid containing a compound having a conjugated double bond, or a modification method of a polyurethane, including the steps of: preparing a polyurethane having a conjugated double bond; and treating the polyurethane with a liquid containing a compound having an ethylenically unsaturated bond is used.