Abstract: A molecular sieve complex contains an oxide of aluminum, an oxide of an alkaline earth metal and a rare earth-modified molecular sieve. The rare earth-modified molecular sieve is a molecular sieve doped by a rare earth element. The percentage of the pore volume occupied by pores of 3 nm or less to the total pore volume in the molecular sieve complex is greater than or equal to 63.5%. The content of the rare earth element and the contents of the oxide of aluminum, the oxide of the alkaline earth metal and the molecular sieve satisfy a certain relationship. The composite material contains a molecular sieve complex and an auxiliary agent loaded on the molecular sieve complex, and the composite material may be applied to flue gas adsorption and desulfurization.

Abstract: A composite material is used for desulfurization. The composite material contains activated carbon, alkali metal oxides, silicon oxides, iron oxides, and rare earth element oxides. The weight ratio among the activated carbon, iron oxides and rare earth element oxides is 100:(0.5-5):(1-10). The composite material, used as a sulfur adsorbent, has a higher sulfur breakthrough capacity and desulfurization rate.

Abstract: A catalyst can be used for removing carbonyl sulfide in natural gas. The catalyst has a carrier, and an alkali metal oxide and nickel oxide which are loaded on the carrier. Based on the total weight of the catalyst, the content of the carrier is 90-97 wt %, the content of the alkali metal oxide is 2-6 wt %, and the content of the nickel oxide is 1-4 wt %. At least part of the carrier is AlO(OH), ?-Al2O3 and ?-Al2O3 phases. The catalyst can achieve a COS conversion rate of greater than or equal to 99% and a service life of 8 years or above, and can effectively reduce the content of carbonyl sulfur in natural gas.

Abstract: A composite material is used for desulfurization. The composite material contains activated carbon, alkali metal oxides, silicon oxides, iron oxides, and rare earth element oxides. The weight ratio among the activated carbon, iron oxides and rare earth element oxides is 100:(0.5-5):(1-10). The composite material, used as a sulfur adsorbent, has a higher sulfur breakthrough capacity and desulfurization rate.

Abstract: A molecular sieve complex contains an oxide of aluminum, an oxide of an alkaline earth metal and a rare earth-modified molecular sieve. The rare earth-modified molecular sieve is a molecular sieve doped by a rare earth element. The percentage of the pore volume occupied by pores of 3 nm or less to the total pore volume in the molecular sieve complex is greater than or equal to 63.5%. The content of the rare earth element and the contents of the oxide of aluminum, the oxide of the alkaline earth metal and the molecular sieve satisfy a certain relationship. The composite material contains a molecular sieve complex and an auxiliary agent loaded on the molecular sieve complex, and the composite material may be applied to flue gas adsorption and desulfurization.

Abstract: A method for treating sulfur-containing exhaust gases is provided, comprising the following steps: step i): mixing the sulfur-containing exhaust gases, air, and a hydrocarbon fuel, and controlling a reaction between the air and the hydrocarbon fuel therein, to obtain a procedure gas stream comprising the sulfur-containing exhaust gases, hydrogen, and carbon oxides; step ii): controlling a hydrogenation reaction between the hydrogen contained in the procedure gas stream and a sulfur-containing substance in the sulfur-containing exhaust gases, to obtain hydrogenated tail gases containing hydrogen sulfide; and step iii): absorbing the hydrogen sulfide contained in the hydrogenated tail gases with an absorbing agent to obtain purified tail gases.

Abstract: A method for treating sulfur-containing exhaust gases is provided, comprising the following steps: step i): mixing the sulfur-containing exhaust gases, air, and a hydrocarbon fuel, and controlling a reaction between the air and the hydrocarbon fuel therein, to obtain a procedure gas stream comprising the sulfur-containing exhaust gases, hydrogen, and carbon oxides; step ii): controlling a hydrogenation reaction between the hydrogen contained in the procedure gas stream and a sulfur-containing substance in the sulfur-containing exhaust gases, to obtain hydrogenated tail gases containing hydrogen sulfide; and step iii): absorbing the hydrogen sulfide contained in the hydrogenated tail gases with an absorbing agent to obtain purified tail gases.

Abstract: The present invention relates to a method for processing a sulfur-containing gas and a hydrogenation catalyst used therefor. The method comprises introducing the sulfur-containing gas into the tail gas hydrogenation unit of a sulfur recovery device, processing it with the hydrogenation catalyst of the present invention, and absorbing the hydrogenated tail gas with a solvent. The hydrogenation catalyst comprises from 0.5 to 3 wt. % of an active component nickel oxide, from 1 to 4 wt. % of an active component cobalt oxide, from 8 to 20 wt. % of an active component molybdenum oxide or tungsten oxide, from 1 to 5 wt. % of a deoxidation auxiliary agent, from 10 to 40 wt. % of TiO2, the balance being ?-Al2O3, based on the weight of the catalyst.

Abstract: The present invention relates to a method for processing a sulfur-containing gas and a hydrogenation catalyst used therefor. Said method comprises introducing the sulfur-containing gas into the tail gas hydrogenation unit of a sulfur recovery device, processing it with the hydrogenation catalyst of the present invention, absorbing the hydrogenated tail gas with a solvent and then regenerating, the regenerated hydrogen sulfide being recycled to the Claus unit to recover sulfur, the clean tail gas being incinerated in an incinerator to be discharged after reaching the standards. Said sulfur-containing gas comprises from 0 to 6 vol. % of sulfur dioxide and from 0 to 3 vol. % of oxygen, and has a temperature of from 100 to 200° C. The hydrogenation catalyst of the present invention comprises from 0.5 to 3 wt. % of an active component nickel oxide, from 1 to 4 wt. % of an active component cobalt oxide, from 8 to 20 wt. % of an active component molybdenum oxide or tungsten oxide, from 1 to 5 wt.