Methods for preparing isotopically modified 1,4-diene systems from non-isotopically modified 1,4-dienes involve selective oxidation of one or more bis-allylic position(s), or the preparation of isotopically modified 1,4-diene systems via trapping pi-allylic complexes with a source of deuterium or tritium. Such methods are useful for preparing isotopically modified polyunsaturated lipid including polyunsaturated fatty acids and polyunsaturated fatty acid derivatives.

Methods for preparing isotopically modified 1,4-diene systems from non-isotopically modified 1,4-dienes involve selective oxidation of one or more bis-allylic position(s), or the preparation of isotopically modified 1,4-diene systems via trapping pi-allylic complexes with a source of deuterium or tritium. Such methods are useful for preparing isotopically modified polyunsaturated lipid including polyunsaturated fatty acids and polyunsaturated fatty acid derivatives.

A process for preparing a random copolymer based on at least one acyclic diene monomers and on at least one cyclic diene monomer is provided. The process comprises a step of copolymerization, in the presence of a polar agent and an anionic initiator in a polymerization solvent, of at least one acyclic diene monomer and of at least one cyclic diene monomer of which one C═C double bond is endocyclic and conjugated to an exocyclic C═C double bond, at a polymerization temperature below 80° C. A molar ratio of the polar agent/function(s) of the anionic initiator capable of initiating anionic polymerization being greater than 0.1. Copolymers based on at least one acyclic diene monomer and on at least one cyclic diene monomer and the compositions containing them are also provided.

A process for preparing a random copolymer based on at least one acyclic diene monomers and on at least one cyclic diene monomer is provided. The process comprises a step of copolymerization, in the presence of a polar agent and an anionic initiator in a polymerization solvent, of at least one acyclic diene monomer and of at least one cyclic diene monomer of which one C═C double bond is endocyclic and conjugated to an exocyclic C═C double bond, at a polymerization temperature below 80° C. A molar ratio of the polar agent/function(s) of the anionic initiator capable of initiating anionic polymerization being greater than 0.1. Copolymers based on at least one acyclic diene monomer and on at least one cyclic diene monomer and the compositions containing them are also provided.

Relatively low value disulfide oil (DSO) compounds produced as by-products of the mercaptan oxidation (MEROX) processing of refinery hydrocarbon streams, and oxidized disulfide oils (ODSO), are economically converted to value-added BTX by introducing the DSO and/or ODSO compounds as the feed to a fluidized catalytic cracking (FCC) unit and recovering the liquid products. The liquid FCC products are introduced as the feedstream to a selective naphtha hydrogenation and hydrotreating process for desulfurization and are then further separated in an aromatics extraction process for the recovery of BTX.

Relatively low value disulfide oil (DSO) compounds produced as by-products of the mercaptan oxidation (MEROX) processing of refinery hydrocarbon streams, and oxidized disulfide oils (ODSO), are economically converted to value-added BTX by introducing the DSO and/or ODSO compounds as the feed to a fluidized catalytic cracking (FCC) unit and recovering the liquid products. The liquid FCC products are introduced as the feedstream to a selective naphtha hydrogenation and hydrotreating process for desulfurization and are then further separated in an aromatics extraction process for the recovery of BTX.

Methods for preparing isotopically modified 1,4-diene systems from non-isotopically modified 1,4-dienes involve selective oxidation of one or more bis-allylic position(s), or the preparation of isotopically modified 1,4-diene systems via trapping pi-allylic complexes with a source of deuterium or tritium. Such methods are useful for preparing isotopically modified polyunsaturated lipid including polyunsaturated fatty acids and polyunsaturated fatty acid derivatives.

Methods for preparing isotopically modified 1,4-diene systems from non-isotopically modified 1,4-dienes involve selective oxidation of one or more bis-allylic position(s), or the preparation of isotopically modified 1,4-diene systems via trapping pi-allylic complexes with a source of deuterium or tritium. Such methods are useful for preparing isotopically modified polyunsaturated lipid including polyunsaturated fatty acids and polyunsaturated fatty acid derivatives.

Methods for preparing isotopically modified 1,4-diene systems from non-isotopically modified 1,4-dienes involve selective oxidation of one or more bis-allylic position(s), or the preparation of isotopically modified 1,4-diene systems via trapping pi-allylic complexes with a source of deuterium or tritium. Such methods are useful for preparing isotopically modified polyunsaturated lipid including polyunsaturated fatty acids and polyunsaturated fatty acid derivatives.

Methods for preparing isotopically modified 1,4-diene systems from non-isotopically modified 1,4-dienes involve selective oxidation of one or more bis-allylic position(s), or the preparation of isotopically modified 1,4-diene systems via trapping pi-allylic complexes with a source of deuterium or tritium. Such methods are useful for preparing isotopically modified polyunsaturated lipid including polyunsaturated fatty acids and polyunsaturated fatty acid derivatives.