Process for transformation of a feedstock of lignocellulosic biomass and/or the carbohydrates, into mono-oxidized or poly-oxidized compounds, wherein the feedstock is contacted, simultaneously, with a catalytic system that comprises one or more homogeneous catalysts selected from Brønsted acids and heterogeneous catalysts comprising at least one metal selected from groups 6 to 11 and 14 of the periodic table, and a substrate selected from perovskites of formula ABO.sub.3, in which A is Mg, Ca, Sr, Ba, and La, and B is selected from Fe, Mn, Ti and Zr, oxides of lanthanum, neodymium, yttrium, cerium, and niobium, or mixtures thereof, and mixed oxides of aluminates of zinc, copper, and cobalt, or mixtures thereof, in the same reaction chamber, with at least one solvent, being water or water with at least one other solvent, under reducing atmosphere, and temperature of 50° C. to 300° C., and pressure of 0.5 MPa to 20 MPa.

A method for separating monoethylene glycol (MEG) from one or more oxygenates. The method includes providing a stream comprising MEG and one or more oxygenates to a distillation column, providing a water feed stream to a bottom of the distillation column, and removing a recovery stream comprising MEG from the distillation column. The distillation column is operated at higher temperatures than the thermal stability of MEG and the one or more oxygenates.

A method for separating monoethylene glycol (MEG) from one or more oxygenates. The method includes providing a stream comprising MEG and one or more oxygenates to a distillation column, providing a water feed stream to a bottom of the distillation column, and removing a recovery stream comprising MEG from the distillation column. The distillation column is operated at higher temperatures than the thermal stability of MEG and the one or more oxygenates.

A process for bio-1,3-butanediol purification from a fermentation broth includes the steps of: (a) subjecting the fermentation broth to separation, (b) subjecting the product obtained in step (a) to treatment with ion-exchange resins, (c) subjecting the product obtained in step (b) to a first evaporation, (d) subjecting the product obtained in step (c) to a second evaporation; and (e) subjecting the product obtained in step (d) to a third evaporation, obtaining purified bio-1,3-butanediol. The purified bio-1,3-butanediol can be used to produce bio-1,3-butadiene. Bio-1,3-butadiene can be used as a monomer or as an intermediate to produce elastomers and (co)polymers.

A process for bio-1,3-butanediol purification from a fermentation broth includes the steps of: (a) subjecting the fermentation broth to separation, (b) subjecting the product obtained in step (a) to treatment with ion-exchange resins, (c) subjecting the product obtained in step (b) to a first evaporation, (d) subjecting the product obtained in step (c) to a second evaporation; and (e) subjecting the product obtained in step (d) to a third evaporation, obtaining purified bio-1,3-butanediol. The purified bio-1,3-butanediol can be used to produce bio-1,3-butadiene. Bio-1,3-butadiene can be used as a monomer or as an intermediate to produce elastomers and (co)polymers.

In a method and a system for decolorizing and deodorizing a polyhydric alcohol according to embodiments of the present invention, a mixture liquid containing a first polyhydric alcohol obtained by a separation process is prepared. The mixture liquid is subjected to a distillation treatment to preliminarily remove substances with different colors and odors to generate a pre-treatment liquid. The pre-treatment liquid is subjected to an adsorption treatment. Through a combination of the distillation treatment and the adsorption treatment, the removing efficiency of the substances with different colors and odors can be increased.

A process of co-feeding gaseous ethylene with liquid allyl alcohol in the presence of a catalyst to produce 1,4-butanediol and n-propanol may include: introducing a gaseous mixture of ethylene, carbon monoxide and hydrogen into a reactor in the presence of a hydroformylation catalyst in a solvent; introducing liquid allyl alcohol (AA) into the reactor; and carrying out hydroformylation reaction at a temperature between 50 and 100° C. to obtain hydroformylation products.

A process of co-feeding gaseous ethylene with liquid allyl alcohol in the presence of a catalyst to produce 1,4-butanediol and n-propanol may include: introducing a gaseous mixture of ethylene, carbon monoxide and hydrogen into a reactor in the presence of a hydroformylation catalyst in a solvent; introducing liquid allyl alcohol (AA) into the reactor; and carrying out hydroformylation reaction at a temperature between 50 and 100° C. to obtain hydroformylation products.

The invention relates to a two-way approach to isolate, recover and upgrade 2,3-Butanediol (2,3-BDO) from fermentation broth. A complete separation and recovery process for 2,3-BDO using acetalization and trans-acetalization sequence. Acetalization with butyraldehyde using heterogeneous catalysts, either Amberlyst-15® or Nafion NR50®, efficiently isolates 2,3-BDO as phase-separated protected dioxolane. The approach provides significant process advantages with easy product recovery and high recyclability of the catalyst. Trans-acetalization of dioxolane with methanol (methanolysis) followed by distillation of acetal, yielded very high purity 2,3-BDO with about 90% isolated yield. Alternatively, dioxolane is used in a process direct to methyl ethyl ketone (MEK) as a BDO synthon allowing for recovery of the aldehyde.

The invention relates to a two-way approach to isolate, recover and upgrade 2,3-Butanediol (2,3-BDO) from fermentation broth. A complete separation and recovery process for 2,3-BDO using acetalization and trans-acetalization sequence. Acetalization with butyraldehyde using heterogeneous catalysts, either Amberlyst-15® or Nafion NR50®, efficiently isolates 2,3-BDO as phase-separated protected dioxolane. The approach provides significant process advantages with easy product recovery and high recyclability of the catalyst. Trans-acetalization of dioxolane with methanol (methanolysis) followed by distillation of acetal, yielded very high purity 2,3-BDO with about 90% isolated yield. Alternatively, dioxolane is used in a process direct to methyl ethyl ketone (MEK) as a BDO synthon allowing for recovery of the aldehyde.