The present disclosure related generally to a high-temperature water-gas shift catalyst composition comprising: a ZnO phase, present in the composition in an amount of 5-70 wt. %; a zinc-aluminum spinel phase, present in the composition in an amount of 30-95 wt. %; wherein the molar ratio of Zn atoms to Al atoms in the catalyst composition is at least 1:1.

The present disclosure related generally to a high-temperature water-gas shift catalyst composition comprising: a ZnO phase, present in the composition in an amount of 5-70 wt. %; a zinc-aluminum spinel phase, present in the composition in an amount of 30-95 wt. %; wherein the molar ratio of Zn atoms to Al atoms in the catalyst composition is at least 1:1.

The present invention relates to a selective catalytic reduction catalyst for the treatment of an exhaust gas of a diesel engine comprising: a flow-through substrate comprising an inlet end, an outlet end, a substrate axial length extending from the inlet end to the outlet end and a plurality of passages defined by internal walls of the flow through substrate extending therethrough; a coating disposed on the surface of the internal walls of the substrate, wherein the coating comprises a non-zeolitic oxidic material comprising manganese and one or more of the metals of the groups 4 to 11 and 13 of the periodic table, and further comprises one or more of a vanadium oxide and a zeolitic material comprising one or more of copper and iron.

The present invention relates to a selective catalytic reduction catalyst for the treatment of an exhaust gas of a diesel engine comprising: a flow-through substrate comprising an inlet end, an outlet end, a substrate axial length extending from the inlet end to the outlet end and a plurality of passages defined by internal walls of the flow through substrate extending therethrough; a coating disposed on the surface of the internal walls of the substrate, wherein the coating comprises a non-zeolitic oxidic material comprising manganese and one or more of the metals of the groups 4 to 11 and 13 of the periodic table, and further comprises one or more of a vanadium oxide and a zeolitic material comprising one or more of copper and iron.

The present invention relates to a catalyst for the oxidation of NO, for the oxidation of ammonia, for the oxidation of HC and for the selective catalytic reduction of NOx, comprising a flow through substrate comprising an inlet end, an outlet end, a substrate axial length extending from the inlet end to the outlet end and a plurality of passages defined by internal walls of the flow through substrate extending therethrough; a first coating comprising one or more of a vanadium oxide and a zeolitic material comprising one or more of copper and iron; a second coating comprising a first platinum group metal component supported on a non-zeolitic first oxidic material and further comprising one or more of a vanadium oxide and a zeolitic material comprising one or more of copper and iron; optionally a third coating comprising a second platinum group metal component supported on a second oxidic material; wherein the third coating is disposed on the surface of the internal walls and under the second coating over z % of the axial length of the substrate from the outlet end to the inlet end, with z being in the range of from 0 to 100; wherein the second coating extends over y % of the axial length of the substrate from the inlet end to the outlet end and is disposed either on the surface of the internal walls, or on the surface of the internal walls and the third coating, or on the third coating, with y being in the range of from 95 to 100; wherein the first coating extends over x % of the axial length of the substrate from the inlet end to the outlet end and is disposed on the second coating, with x being in the range of from 20 to y.

The present invention relates to a catalyst for the oxidation of NO, for the oxidation of ammonia, for the oxidation of HC and for the selective catalytic reduction of NOx, comprising a flow through substrate comprising an inlet end, an outlet end, a substrate axial length extending from the inlet end to the outlet end and a plurality of passages defined by internal walls of the flow through substrate extending therethrough; a first coating comprising one or more of a vanadium oxide and a zeolitic material comprising one or more of copper and iron; a second coating comprising a first platinum group metal component supported on a non-zeolitic first oxidic material and further comprising one or more of a vanadium oxide and a zeolitic material comprising one or more of copper and iron; optionally a third coating comprising a second platinum group metal component supported on a second oxidic material; wherein the third coating is disposed on the surface of the internal walls and under the second coating over z % of the axial length of the substrate from the outlet end to the inlet end, with z being in the range of from 0 to 100; wherein the second coating extends over y % of the axial length of the substrate from the inlet end to the outlet end and is disposed either on the surface of the internal walls, or on the surface of the internal walls and the third coating, or on the third coating, with y being in the range of from 95 to 100; wherein the first coating extends over x % of the axial length of the substrate from the inlet end to the outlet end and is disposed on the second coating, with x being in the range of from 20 to y.

An SCR catalyst for treating diesel exhaust gas has: a flow-through substrate with an inlet end, an outlet end, a substrate axial length extending from the inlet end to the outlet end and a plurality of passages defined by internal walls of the flow through substrate extending therethrough; a first coating disposed on the internal wall surface of the substrate, the surface defining the interface between the internal walls and passages, the first coating extending over 40 to 100% of the substrate axial length, the first coating having an 8-membered ring pore zeolitic material with copper and/or iron; a second coating extending over 20 to 100% of the substrate axial length, the second coating having a first oxidic material with titania, wherein at least 75 wt. % of the second coating is titania, calculated as TiO.sub.2, and 0 to 0.01 wt. % of the second coating is vanadium oxides, calculated as V.sub.2O.sub.5.

An SCR catalyst for treating diesel exhaust gas has: a flow-through substrate with an inlet end, an outlet end, a substrate axial length extending from the inlet end to the outlet end and a plurality of passages defined by internal walls of the flow through substrate extending therethrough; a first coating disposed on the internal wall surface of the substrate, the surface defining the interface between the internal walls and passages, the first coating extending over 40 to 100% of the substrate axial length, the first coating having an 8-membered ring pore zeolitic material with copper and/or iron; a second coating extending over 20 to 100% of the substrate axial length, the second coating having a first oxidic material with titania, wherein at least 75 wt. % of the second coating is titania, calculated as TiO.sub.2, and 0 to 0.01 wt. % of the second coating is vanadium oxides, calculated as V.sub.2O.sub.5.

A visible light catalyst, its preparation method, a visible light catalyst activated persulfate system and its use. The visible light catalyst includes a carbon material, a transition metal compound and a coating material. The carbon material is conductive carbon material, and the transition metal compound is selected from one or more of transition metal oxides, transition metal sulfides, and acid or salt compounds containing a transition metal. The visible light catalyst has high visible light photocatalytic activity and performance of degrading organic pollutants and activating persulfate which can result in synergistically degrading degradation-resistant organic pollutants.

The present disclosure provides a method for the oxidative dehydrogenation of an alkane, e.g., ethane, propane, etc. In embodiments, a method for oxidative dehydrogenation of an alkane comprises exposing a gas comprising an alkane having 2 or more carbons to elemental sulfur vapor at an elevated reaction temperature and for a period of time to convert the alkane to one or more products via oxidative dehydrogenation, the one or more products comprising a primary alkene.