Patent classifications
C07D223/10
Process for the purification of caprolactam from a solution of crude caprolactam without organic solvent extraction
The present invention relates to a process for purifying caprolactam from solutions of cmde caprolactam by a direct treatment with one or more alkaline compounds of polyvalent metals, preferably bivalent and trivalent, without resorting to organic solvent extraction as used in the usual purification process. A further subject of the present invention is a facility devoid of a unit for organic solvent extraction and designed to carry out the caprolactam purification process described herein.
Process for the purification of caprolactam from a solution of crude caprolactam without organic solvent extraction
The present invention relates to a process for purifying caprolactam from solutions of cmde caprolactam by a direct treatment with one or more alkaline compounds of polyvalent metals, preferably bivalent and trivalent, without resorting to organic solvent extraction as used in the usual purification process. A further subject of the present invention is a facility devoid of a unit for organic solvent extraction and designed to carry out the caprolactam purification process described herein.
Homogeneous Catalysts That Are Recoverable By Host Guest Interactions
A method for separating a homogeneous catalyst from a solution includes forming a host-guest compound between a first isomer of the catalyst and inclusion compound in the solution and isolating the host-guest compound from the solution. The catalyst may be released from the inclusion compound by converting the first isomer of the catalyst to a second isomer of the catalyst.
Homogeneous Catalysts That Are Recoverable By Host Guest Interactions
A method for separating a homogeneous catalyst from a solution includes forming a host-guest compound between a first isomer of the catalyst and inclusion compound in the solution and isolating the host-guest compound from the solution. The catalyst may be released from the inclusion compound by converting the first isomer of the catalyst to a second isomer of the catalyst.
SELECTIVE DEPOLYMERISATION OF POLYAMIDE 6 TO PRODUCE CAPROLACTAM FROM MIXTURES OF CAPROLACTAM-CONTAINING POLYMERS AND POLYURETHANE-CONTAINING POLYMERS, IN PARTICULAR POLYURETHANE BLOCK COPOLYMERS
A process for obtaining caprolactam from mixtures of caprolactam-containing polymers and polyurethane-containing polymers, in particular polyurethane block copolymers, by depolymerization, wherein the depolymerization of the mixture is performed in the presence of 0.05% to 5% by weight of a base at a temperature of 250? C. to 350? C. and a pressure of 5 to 700 mbar and wherein the caprolactam is obtained in gaseous form.
SELECTIVE DEPOLYMERISATION OF POLYAMIDE 6 TO PRODUCE CAPROLACTAM FROM MIXTURES OF CAPROLACTAM-CONTAINING POLYMERS AND POLYURETHANE-CONTAINING POLYMERS, IN PARTICULAR POLYURETHANE BLOCK COPOLYMERS
A process for obtaining caprolactam from mixtures of caprolactam-containing polymers and polyurethane-containing polymers, in particular polyurethane block copolymers, by depolymerization, wherein the depolymerization of the mixture is performed in the presence of 0.05% to 5% by weight of a base at a temperature of 250? C. to 350? C. and a pressure of 5 to 700 mbar and wherein the caprolactam is obtained in gaseous form.
Anti-Fibrotic Pyridinones
Disclosed are pyridinone compounds, method for preparing these compounds, and methods for treating fibrotic disorders.
Anti-Fibrotic Pyridinones
Disclosed are pyridinone compounds, method for preparing these compounds, and methods for treating fibrotic disorders.
Use of agonists of formyl peptide receptor 2 for treating dermatological diseases
The present invention relates to a method for treating dermal inflammation and dermal diseases by local or systemic delivery, in a subject in need of such treatment, which comprises administering a pharmaceutical composition comprising a therapeutically effective amount of at least one agonist of Formyl peptide receptor 2 (FPR2).
Use of agonists of formyl peptide receptor 2 for treating dermatological diseases
The present invention relates to a method for treating dermal inflammation and dermal diseases by local or systemic delivery, in a subject in need of such treatment, which comprises administering a pharmaceutical composition comprising a therapeutically effective amount of at least one agonist of Formyl peptide receptor 2 (FPR2).