One or more concentrated low-viscosity solutions of alkaline earth alkoxide compounds M(OCH.sub.2R.sup.6).sub.2-a-b(OR.sup.7).sub.a[O(CHR.sup.8).sub.nOR.sup.9].sub.b in mixture with a metal alkyl compound M(R.sup.10R.sup.11) in an aprotic solvent and related methods are disclosed herein.

One or more concentrated low-viscosity solutions of alkaline earth alkoxide compounds M(OCH.sub.2R.sup.6).sub.2-a-b(OR.sup.7).sub.a[O(CHR.sup.8).sub.nOR.sup.9].sub.b in mixture with a metal alkyl compound M(R.sup.10R.sup.11) in an aprotic solvent and related methods are disclosed herein.

The present invention relates to an integrated process for simultaneously preparing at least two mixtures comprising alkali metal methoxide and methanol in at least two parallel reactive distillation columns, wherein one rectification column is used for providing a methanol stream which is then used as methanol source for the reactive distillation columns, and wherein the top streams of said reactive distillation columns are used as methanol source for said rectification column.

The present invention relates to an integrated process for simultaneously preparing at least two mixtures comprising alkali metal methoxide and methanol in at least two parallel reactive distillation columns, wherein one rectification column is used for providing a methanol stream which is then used as methanol source for the reactive distillation columns, and wherein the top streams of said reactive distillation columns are used as methanol source for said rectification column.

A method for manufacturing calcium diglyceroxide crystals includes at least the following steps: placing at least one calcium element source compound, in particular calcium oxide, in suspension in glycerol or in a homogeneous mixture of glycerol and an anhydrous glycerol solvent, in particular methanol, referred to as the starting suspension, the molar ratio being greater than or equal to 2; milling the starting suspension at an ambient temperature of less than or equal to 50 C. in a three-dimensional liquid-phase ball mill for a holding time of 15 minutes or less; recovering, at the outlet of the mill, a suspension of calcium diglyceroxide crystals, and optionally, washing the obtained suspension with a glycerol solvent in order to eliminate any excess glycerol, optionally, drying the suspension of calcium diglyceroxide crystals so as to obtain a powder of calcium diglyceroxide crystals. Also disclosed are uses associated with the calcium diglyceroxide crystals.

A method for manufacturing calcium diglyceroxide crystals includes at least the following steps: placing at least one calcium element source compound, in particular calcium oxide, in suspension in glycerol or in a homogeneous mixture of glycerol and an anhydrous glycerol solvent, in particular methanol, referred to as the starting suspension, the molar ratio being greater than or equal to 2; milling the starting suspension at an ambient temperature of less than or equal to 50 C. in a three-dimensional liquid-phase ball mill for a holding time of 15 minutes or less; recovering, at the outlet of the mill, a suspension of calcium diglyceroxide crystals, and optionally, washing the obtained suspension with a glycerol solvent in order to eliminate any excess glycerol, optionally, drying the suspension of calcium diglyceroxide crystals so as to obtain a powder of calcium diglyceroxide crystals. Also disclosed are uses associated with the calcium diglyceroxide crystals.

One or more concentrated low-viscosity solutions of alkaline earth alkoxide compounds M(OCH.sub.2R.sup.6).sub.2-a-b(OR.sup.7).sub.a[O(CHR.sup.8).sub.nOR.sup.9].sub.b in mixture with a metal alkyl compound M(R.sup.10R.sup.11) in an aprotic solvent and related methods are disclosed herein.

One or more concentrated low-viscosity solutions of alkaline earth alkoxide compounds M(OCH.sub.2R.sup.6).sub.2-a-b(OR.sup.7).sub.a[O(CHR.sup.8).sub.nOR.sup.9].sub.b in mixture with a metal alkyl compound M(R.sup.10R.sup.11) in an aprotic solvent and related methods are disclosed herein.

The present disclosure relates to the formation of dimethyl terephthalate (DMT). The present invention also relates to the depolymerization of polyethylene terephthalate (PET) and the recovery of dimethyl terephthalate (DMT).

The present disclosure relates to the formation of dimethyl terephthalate (DMT). The present invention also relates to the depolymerization of polyethylene terephthalate (PET) and the recovery of dimethyl terephthalate (DMT).