The invention relates to a thermal conversion vessel (200) used during amidification step of acetone cyanohydrin (ACH), in the industrial process for production of a methyl methacrylate (MMA) or methacrylic acid (MAA). The thermal conversion vessel (200) is used for converting an hydrolysis mixture of α-hydroxyisobutyramide (HIBAM), α-sulfatoisobutyramide (SIBAM), 2-methacrylamide (MACRYDE) and methacrylique acid (MAA), into a mixture of 2-methacrylamide (MACRYDE). It comprises:—at least one compartment (C1, C2, C3, . . . Ci) comprising an inner wall (206a, 206b, . . . 206i) separating said compartment into two communicating parts (C1a, C1b) by a passage provided between the bottom of said vessel and said inner wall,—said compartment having a space above said inner wall, for separating gas phase from liquid phase during thermal conversion,—said compartment being connected to an outlet valve (204a, 204b, . . . 204i). Such vessel allows obtaining a high yield thermal conversion in very safe conditions.

The invention relates to a thermal conversion vessel (200) used during amidification step of acetone cyanohydrin (ACH), in the industrial process for production of a methyl methacrylate (MMA) or methacrylic acid (MAA). The thermal conversion vessel (200) is used for converting an hydrolysis mixture of α-hydroxyisobutyramide (HIBAM), α-sulfatoisobutyramide (SIBAM), 2-methacrylamide (MACRYDE) and methacrylique acid (MAA), into a mixture of 2-methacrylamide (MACRYDE). It comprises:—at least one compartment (C1, C2, C3, . . . Ci) comprising an inner wall (206a, 206b, . . . 206i) separating said compartment into two communicating parts (C1a, C1b) by a passage provided between the bottom of said vessel and said inner wall,—said compartment having a space above said inner wall, for separating gas phase from liquid phase during thermal conversion,—said compartment being connected to an outlet valve (204a, 204b, . . . 204i). Such vessel allows obtaining a high yield thermal conversion in very safe conditions.

The present invention relates to the use of haloapatites as catalysts of the dehydration reaction of α-hydroxylated carboxylic acids or acid esters, in particular of lactic acid or of methyl lactate, and also to a process for producing unsaturated carboxylic acids or acid esters, in particular acrylic acid or methyl acrylate, in the gas phase in a stainless steel reactor, in the presence of such a catalyst.

The present invention relates to the use of haloapatites as catalysts of the dehydration reaction of α-hydroxylated carboxylic acids or acid esters, in particular of lactic acid or of methyl lactate, and also to a process for producing unsaturated carboxylic acids or acid esters, in particular acrylic acid or methyl acrylate, in the gas phase in a stainless steel reactor, in the presence of such a catalyst.

The present invention relates to the use of haloapatites as catalysts of the dehydration reaction of α-hydroxylated carboxylic acids or acid esters, in particular of lactic acid or of methyl lactate, and also to a process for producing unsaturated carboxylic acids or acid esters, in particular acrylic acid or methyl acrylate, in the gas phase in a stainless steel reactor, in the presence of such a catalyst.

The present invention relates to a method of redissociating Michael adducts of acrylic acid present in a liquid F in a redissociation apparatus comprising at least one separating column K, an evaporator V and a pump P, wherein, in the event of an unwanted rise in the viscosity of the residue R in the bottom space of the separating column K, the feed of the liquid F into the redissociation apparatus is stopped, the residue R in the bottom space of the separating column K is diluted and cooled with a solvent 1, and the bottom space of the separating column K is emptied.

The present invention relates to a method of redissociating Michael adducts of acrylic acid present in a liquid F in a redissociation apparatus comprising at least one separating column K, an evaporator V and a pump P, wherein, in the event of an unwanted rise in the viscosity of the residue R in the bottom space of the separating column K, the feed of the liquid F into the redissociation apparatus is stopped, the residue R in the bottom space of the separating column K is diluted and cooled with a solvent 1, and the bottom space of the separating column K is emptied.

Methods for catalytically dehydrating lactate salt to acrylic acid, acrylate salt, or mixtures thereof with high yield and selectivity and without significant conversion to undesired side products, such as, acetaldehyde, propionic acid, and acetic acid, are provided. The catalysts include acid-base bifunctional catalysts.

Methods for catalytically dehydrating lactate salt to acrylic acid, acrylate salt, or mixtures thereof with high yield and selectivity and without significant conversion to undesired side products, such as, acetaldehyde, propionic acid, and acetic acid, are provided. The catalysts include acid-base bifunctional catalysts.

The present invention relates to an improved process for the regeneration, by thermal cracking, of a mixture of heavy byproducts (residues) resulting from a unit for the production of acrylic acid and from a unit for the production of acrylic ester, resulting in acrylic acid, acrylic esters and alcohols being obtained, for the purpose of recycling them in the plant for the production of the acrylic ester.