Method for making pellet type catalyst

In a method for making pellet-type catalysts the improvement comprising the steps of grinding to the desired size a refractory ceramic support material having a high free alkali metal content of at least about 0.15% based on the weight of said support material, mixing said support material with a combustible organic material formed from a non-acid hydrophobic type thermoplastic material having an average particle size of from about 20 to 30 microns, forming the resulting support and organic materials mixture into pellets of the desired shape and size wherein said organic material is present in an amount of from about 0.12 to 0.5 weight % of said pellet, calcining the pellets to burn-out said organic material and obtain the desired surface area and pore structure, soaking the pellets in a dilute inorganic acid solution having a concentration of from about 0.04 to about 0.15 weight % acid or in a solution of the salt of the acid having an equivalent concentration of acid anion, said soaking being continued for a short period of time of at least about 1 minute such as to avoid removal of any constituents forming the support crystallites and to enable penetration of the acid anions into said pellets to the depth to which it is desired to impregnate the pellets with catalytically active metallic material, draining said solution from said pellets, and impregnating said pellets with a solution of a salt or acid of the catalytically active material to the depth of acid or acid salt treatment, said catalytically active material being at least one of the metals selected from the Groups V-B, VI-B and VIII of the Periodic Table of Elements, and copper, the use of said high alkali metal content refractory ceramic support material resulting in substantial cost savings in support material and enabling control of the depth of catalyst impregnation and pellet surface area.

In a method for making pellet-type catalysts the improvement comprising the steps of grinding to the desired size alumina trihydrate containing a high concentration of free alkali metal of at least about 0.15% based on the weight of said alumina trihydrate, flash calcining said alumina trihydrate to convert it to the amorphous structure, mixing said amorphous alumina with water and a combustible organic material formed from a non-acid hydrophobic type thermoplastic material having an average particle size of from about 20 to 30 microns, sufficient water being mixed with said amorphous alumina and organic material to substantially satisfy the maximum moisture holding capacity of the mixture, forming said mixture into pellets of the desired shape and size, said combustible organic material being present in the pellet in an amount of from about 0.12 to 0.5 weight percent, rehydrating said pellets to the monohydrate form, calcining said pellets to burn-out said organic material and obtain the desired pore structure and surface area, treating said pellets with a dilute inorganic acid water solution having a concentration of from about 0.04 to 0.15 weight percent acid or with a solution of the salt of the acid having an equivalent concentration of acid anion, said acid treatment being continued for a short period of time of at least about 1 minute such as to avoid removal of any constituents forming the support crystallites and to enable penetration of the acid anions into said pellets to the depth to which it is desired to impregnate the pellets with catalytically active metallic material, draining said solution from said pellets, and impregnating said pellets with a solution of a salt or acid of the catalytically active material to said desired depth, said catalytically active material being at least one of the metals selected from the Groups V-B, VI-B and VIII of the Periodic Table of Elements, and copper, the use of said high alkali metal containing alumina trihydrate enabling substantial cost savings and the control of the depth of catalyst penetration and pellet surface area.