A multi-function catalyst article for treating both NO and carbon monoxide emissions in a flow of a combustion exhaust gas from a stationary emission source comprises a honeycomb monolith substrate comprising one or more channels which are open at both ends and extend along an axial length thereof and through which, in use, a combustion exhaust gas flows, which catalyst article comprising a catalyst composition comprising a combination of a first, vanadium-containing SCR catalyst component and a second component which is a compound of a transition metal comprising copper, manganese, cobalt, molybdenum, nickel or cerium or a mixture of any two or more thereof and optionally a third, crystalline molecular sieve component.

An iron-free supported catalyst for the selective conversion of hydrocarbons to carbon nanotubes may include cobalt and vanadium as active catalytic metals in any oxidation state on a catalyst support comprising aluminum oxide hydroxide. The mass ratio of cobalt to vanadium is between 2 and 15; the mass ratio of cobalt to aluminum is between 5.8 10.sup.−2 and 5.8 10.sup.−1; and the mass ratio vanadium to aluminum is between 5.8 10.sup.−3 and 8.7 10.sup.−2. The present disclosure is further related to a method for the production of this iron-free supported catalyst and to a method for the production of carbon nanotubes using the iron-free supported catalyst.

The present invention relates to a supported catalyst for producing carbon nanotubes which includes a carrier having a number average particle size (D.sub.MN) of 1.5 μm to 20 μm, and an active ingredient supported in the carrier, wherein the active ingredient which prevents the aggregation between particles and supports the particles may act as an active ingredient, so that it is possible to provide a supported catalyst which has excellent activity, and thus, which may improve the production yield.

As a visible-light-responsive photocatalytic-titanium-oxide-particulate dispersion liquid that can achieve a high visible light activity and is of a type different from the related art, the present invention provides a visible-light-responsive photocatalytic-titanium-oxide-particulate dispersion liquid in which two types of titanium oxide particulates are dispersed in an aqueous dispersion medium. The two types of titanium oxide particulates are first titanium oxide particulates, in which a tin component and a transition metal component (but excluding an iron-group component) for enhancing visible light responsiveness are dissolved, and second titanium oxide particulates, in which an iron-group component is dissolved. When a photocatalytic film formed by using this dispersion liquid is used, a high decomposition activity is achieved even in a case where a decomposition substrate has low concentration, which was previously difficult under visible light conditions.

The present invention relates to a bundle-type carbon nanotube which has a bulk density of 25 to 45 kg/m.sup.3, a ratio of the bulk density to a production yield of 1 to 3, and a ratio of a tap density to the bulk density of 1.3 to 2.0, and a method for preparing the same.

A hybrid photoactive heterojunction including a copper vanadate, Cu.sub.2V.sub.2O.sub.7 (CVO) and a zinc vanadate, Zn.sub.2V.sub.2O.sub.6 (ZVO). Particles of the ZVO are dispersed in particles of the CVO to form the hybrid photoactive heterojunction. The hybrid photoactive heterojunction in the form of a photoactive film includes a substrate which is at least partially coated with the hybrid photoactive heterojunction. A method of photodegrading a dye includes contacting the photoactive film and the dye in a solution and exposing the solution to light. A method of photoelectrochemically oxidizing water includes contacting the photoactive film with water in a solution and exposing the solution to light.

Provided is a catalyst which, when used in a selective catalytic reduction reaction in which ammonia serves as the reducing agent, further improves denitration efficiency at low temperatures compared to the prior art.

The denitration catalyst comprises vanadium oxide as a main component, and has a content of a second metal, in teams of oxide, of 1-40 wt %. The second metal is at least one type of metal element selected from the group consisting of Co, W, Mo, Nb, Ce, Sn, Ni, Fe, Cu, Zn, and Mn.

In order to specify a catalytic converter, especially SCR catalytic converter, with maximum catalytic activity, this catalytic converter has at least one catalytically active component and additionally at least one porous inorganic filler component having meso- or macroporosity. The organic porous filler component has a proportion of about 5 to 50% by weight. More particularly, a diatomaceous earth or a pillared clay material is used as the porous inorganic filler component.

The present invention relates to a selective catalytic reduction catalyst for the treatment of an exhaust gas of a diesel engine comprising (i) 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; (II) a coating disposed on the surface of the internal walls of the substrate, where-in the surface defines the interface between the passages and the internal walls, wherein the coating comprises a vanadium oxide supported on an oxidic material comprising titania, and further comprises a mixed oxide of vanadium and one or more of iron, erbium, bismuth, cerium, europium, gadolinium, holmium, lanthanum, lutetium, neodymium, praseodymium, promethium, samarium, scandium, terbium, thulium, ytterbium, yttrium, molybdenum, tungsten, manganese, cobalt, nickel, copper, aluminum and antimony.

The invention relates to a V—Ni.sub.2P/g-C.sub.3N.sub.4 photocatalyst, a preparation method, and application thereof. The V—Ni.sub.2P/g-C.sub.3N.sub.4 photocatalyst is a composite material of V—Ni.sub.2P and g-C.sub.3N.sub.4, wherein V—Ni.sub.2P has the spherical structure formed by nanosheets; the mass ratio of the V—Ni.sub.2P and g-C.sub.3N.sub.4 is (0.01 to 0.2):1.