The invention relates to a method for storing and re-releasing dihydrogen (1) comprising at least: a step of generating hydrogen (G) by dehydrogenating hydroxyl groups of dipropylene glycol into respective carbonyl groups, in order to produce a dehydrogenated substrate (SD) and gaseous dihydrogen (H.sub.2), a step of regenerating (R) at least a portion of the dipropylene glycol (DG), by hydrogenating said carbonyl groups into respective hydroxyl groups by means of gaseous dihydrogen (H.sub.2).

The invention is particularly suitable for storing dihydrogen as an energy carrier.

The invention relates to a method for storing and re-releasing dihydrogen (1) comprising at least: a step of generating hydrogen (G) by dehydrogenating hydroxyl groups of dipropylene glycol into respective carbonyl groups, in order to produce a dehydrogenated substrate (SD) and gaseous dihydrogen (H.sub.2), a step of regenerating (R) at least a portion of the dipropylene glycol (DG), by hydrogenating said carbonyl groups into respective hydroxyl groups by means of gaseous dihydrogen (H.sub.2).

The invention is particularly suitable for storing dihydrogen as an energy carrier.

A method for recovering mono-propylene glycol from a mixture comprising bio-derived diols and an organic impurity is disclosed. The method may comprise: (ia) separating the organic impurity from mono-propylene glycol in a first distillation process, wherein the first distillation process is carried out at a temperature within the range of 140-200° C. and a pressure within the range of 0.3-1.0 bar; and (ii) recovering mono-propylene glycol. Further is disclosed mono-propylene glycol obtainable by the method.

The present disclosure relates to a process for manufacturing 2,3-butanediol by electroreduction of 3-hydroxybutan-one in an aqueous media.

The present disclosure relates to pouches made from a combination of chemically different water-soluble films and optionally containing a composition (e.g. a household care composition or non-household care composition) that is at least partially enclosed by the water-soluble films in at least one compartment.

The present disclosure relates to water-soluble unit dose articles made from a combination of chemically different water-soluble films and optionally containing compositions that are at least partially enclosed by the water-soluble films in at least one compartment.

A process of purifying 1,4-butanediol (1,4-BDO) from a fermentation broth including separating solid materials, salts and water, and subjecting the resulting material to a two, three or four column distillation system, that can include a wiped film evaporator to produce a purified 1,4-butanediol.

The invention provides a process for the separation of MEG from a glycol stream comprising MEG and 1,2-BDO, said process comprising the steps of: (a) providing the glycol stream and an azeotrope-forming agent to a distillation column, (b) subjecting the glycol stream and the azeotrope-forming agent to distillation at a distillation temperature and a distillation pressure; (c) obtaining a first overhead stream comprising an azeotrope of MEG and the azeotrope-forming agent and a first bottoms stream comprising 1,2-BDO; and (d) subjecting the first overhead stream to phase separation in the presence of water to obtain an MEG-rich aqueous stream and an azeotrope-forming agent rich stream, wherein the azeotrope-forming agent is an organic solvent that forms a homogeneous azeotrope with MEG and does not form an azeotrope with 1,2-BDO at the distillation temperature and pressure.

The use of a metal complex containing a ruthenium ion or an osmium ion, and a tridentate aminodicarbene ligand, the tridentate aminodicarbene ligand having one secondary amino group and two specific heterocyclic carbene groups sandwiching the amino group, enables hydrogenation reduction of carbonyl compounds, such as ketones, carboxylic acid esters, lactones, carboxylic acid amides, and lactams, and imine compounds under relatively mild conditions to produce corresponding alcohols, amines, and the like in a high yield with high catalytic efficiency. The metal complex is obtained by a method comprising steps of reacting a specific metal compound with a specific aminodicarbene precursor and subsequently reacting a specific compound. Reduction of a carbonyl compound or an imine compound in the presence of this metal complex using a hydrogen donor makes it possible to reduce the carbonyl compound or imine compound by hydrogenation.

The use of a metal complex containing a ruthenium ion or an osmium ion, and a tridentate aminodicarbene ligand, the tridentate aminodicarbene ligand having one secondary amino group and two specific heterocyclic carbene groups sandwiching the amino group, enables hydrogenation reduction of carbonyl compounds, such as ketones, carboxylic acid esters, lactones, carboxylic acid amides, and lactams, and imine compounds under relatively mild conditions to produce corresponding alcohols, amines, and the like in a high yield with high catalytic efficiency. The metal complex is obtained by a method comprising steps of reacting a specific metal compound with a specific aminodicarbene precursor and subsequently reacting a specific compound. Reduction of a carbonyl compound or an imine compound in the presence of this metal complex using a hydrogen donor makes it possible to reduce the carbonyl compound or imine compound by hydrogenation.