Embodiments provide a method for determining a chloride content of an alumina-based catalyst used for catalytic reforming. The method includes the step of combining nitric acid, isopropanol, and the alumina-based catalyst such that the alumina-based catalyst is dissolved in the nitric acid and the isopropanol to form a homogenized mixture. The alumina-based catalyst include chloride. The method includes the step of taking a conductivity measurement of the homogenized mixture using a pair of electrodes. The method includes the step of introducing a titrant solution comprising silver nitrate to the homogenized mixture such that a precipitate of silver chloride is formed. The method includes the step of determining a chloride concentration of the homogenized mixture based on the conductivity measurement of the homogenized mixture. The method includes the step of determining the chloride content of the alumina-based catalyst based on the chloride concentration of the homogenized mixture.

Embodiments provide a method for determining a chloride content of an alumina-based catalyst used for catalytic reforming. The method includes the step of combining nitric acid, isopropanol, and the alumina-based catalyst such that the alumina-based catalyst is dissolved in the nitric acid and the isopropanol to form a homogenized mixture. The alumina-based catalyst include chloride. The method includes the step of taking a conductivity measurement of the homogenized mixture using a pair of electrodes. The method includes the step of introducing a titrant solution comprising silver nitrate to the homogenized mixture such that a precipitate of silver chloride is formed. The method includes the step of determining a chloride concentration of the homogenized mixture based on the conductivity measurement of the homogenized mixture. The method includes the step of determining the chloride content of the alumina-based catalyst based on the chloride concentration of the homogenized mixture.

A process and method for removing hydrogen sulfide from a gas and regenerating ferric ions consumed in the hydrogen sulfide scrubbing process at low pH. A two-scrubber regenerative chemical scrubbing system for removing hydrogen sulfide from a gas that provides an economical system for removing hydrogen sulfide from a gas at low pH without the need for chelating agents. An oxide of manganese is used as a catalyst to enhance the regeneration of ferric ions in an aqueous solution under acidic conditions in the presence of oxygen. The process may further include contacting the aqueous solution with a second gas comprising air to replenish the dissolved oxygen in the aqueous solution. The regenerated solution comprising ferric ions can be reused to treat additional hydrogen sulfide containing gases.

The present disclosure relates to a method and an apparatus for treating, sorting and recycling an oil-containing discharged catalyst. There is provided a method for treating, sorting and recycling an oil-containing discharged catalyst, wherein the method comprises the following steps: (A) cyclonic washing and on-line activation of a discharged catalyst; (B) cyclonic spinning solvent stripping of the catalyst; (C) gas stream acceleration sorting of a high activity catalyst; (D) cyclonic restriping and particle capture of the high activity catalyst; and (E) cooling of the gas and condensation removal of the solvent. There is further provided an apparatus for treating, sorting and recycling an oil-containing discharged catalyst.

The present disclosure relates to a method and an apparatus for treating, sorting and recycling an oil-containing discharged catalyst. There is provided a method for treating, sorting and recycling an oil-containing discharged catalyst, wherein the method comprises the following steps: (A) cyclonic washing and on-line activation of a discharged catalyst; (B) cyclonic spinning solvent stripping of the catalyst; (C) gas stream acceleration sorting of a high activity catalyst; (D) cyclonic restriping and particle capture of the high activity catalyst; and (E) cooling of the gas and condensation removal of the solvent. There is further provided an apparatus for treating, sorting and recycling an oil-containing discharged catalyst.

A catalyst structure includes a porous support structure, where the support structure includes an aluminosilicate material. Any two or more metals are loaded in the porous support structure, the two or more metals selected from the group consisting of Ga, Ag, Mo, Zn, Co and Ce, where each metal loaded in the porous support structure is present in an amount from about 0.1 wt % to about 20 wt %. In example embodiments, the catalyst structure includes three or more of the metals loaded in the porous support structure. The catalyst structure is used in a hydrocarbon upgrading process that is conducted in the presence of methane, nitrogen or hydrogen.

Methods of treating hydroconversion catalysts used for cracking of hydrocarbons are described. A method can include mixing an inactive hydroconversion catalyst with a solid hydrocarbon containing material having a melting point of 50 C. or greater. The inactive hydroconversion catalyst/solid hydrocarbon containing material mixture can be contacted with a gaseous stream that includes hydrogen (H.sub.2) and a sulfur-containing compound under conditions sufficient to sulfide the catalyst and carbonize at least a portion of the hydrocarbon containing material on the sulfided catalyst to obtain a treated sulfided hydroconversion catalyst.

Methods of treating hydroconversion catalysts used for cracking of hydrocarbons are described. A method can include mixing an inactive hydroconversion catalyst with a solid hydrocarbon containing material having a melting point of 50 C. or greater. The inactive hydroconversion catalyst/solid hydrocarbon containing material mixture can be contacted with a gaseous stream that includes hydrogen (H.sub.2) and a sulfur-containing compound under conditions sufficient to sulfide the catalyst and carbonize at least a portion of the hydrocarbon containing material on the sulfided catalyst to obtain a treated sulfided hydroconversion catalyst.

A method for producing a dicyclopentadiene-modified phenolic resin. The method including reusing a fluorine-based ion-exchange resin as a catalyst in a reaction between a phenol and a dicyclopentadiene, the fluorine-based ion-exchange resin having been used as a catalyst when a phenol and a dicyclopentadiene are allowed to react with each other to produce a first dicyclopentadiene-modified phenolic resin. In the method, the fluorine-based ion-exchange resin is washed with an organic solvent. The dicyclopentadiene-modified phenolic resin obtained by the method has a stable quality, has a high purity, and is inexpensive.

The present invention is an in-situ cleaning procedure for the recovery of catalytic activity of a based alumina HDS catalyst, molybdenum, nickel coated coke and contaminants and it has an HDS activity seriously diminished. The catalyst under study had between 13 and 18 wt % total carbon. Reformate, half the total volume, industrial toluene=35 volume % and Iso-propylic alcohol, 15 volume %, in order to reactivate a deactivated catalyst, a solvent mixture with the following volumetric ratio is prepared. Or it can also be used only reformate (100% volume). The solvent mixture is passed using a LHSV of 2 hr1 for 72 hours at 50 C. or also using a recirculating three 24-hour cycles at 50 C. Option lasts 24 hours pure reformate LHSV=2h1 to 50 C. The washed catalyst is fed back to the load reaction conditions maintained for 36 hours at 340 C., to initiate HDS activity balances. During this treatment oxides of molybdenum and nickel in the active phase are re-sulfided by increasing the HDS activity. The In-Situ Cleaning procedure to reactivate deactivated hydrotreating catalysts used to partially remove the carbon and increase the active phase of molybdenum di-sulphide, and also retrieve specific area, and hydrogenation sites that promote higher hydrodesulfurization activity of gasoil after this treatment.