A catalyst for selectively oxidizing hydrogen sulfide to element sulfur, catalyst for burning tail-gas, and process for deeply catalytically oxidizing hydrogen sulfide to sulfur are disclosed. The catalyst for selectively oxidizing hydrogen sulfide to element sulfur is prepared by: 10-34% of iron trioxide and 60-84% of anatase titanium dioxide, and the balance being are auxiliary agents. Also a catalyst for burning tail-gas is prepared by: 48-78% of iron trioxide and 18-48% of anatase titanium dioxide, and the balance being auxiliary agents. The catalyst of the present invention has high selectivity and high sulfur recovery rate. An isothermal reactor and an adiabatic reactor of the present invention are connected in series and are filled with the above two catalysts for reactions, thus reducing total sulfur in the vented gas while having a high sulfur yield and conversion rate.

A catalyst, including: a transition metal; and an organic solvent. The transition metal is dispersed in the organic solvent in the form of monodisperse nanoparticles; the transition metal has a grain size of between 1 and 100 nm; and the catalyst has a specific surface area of 5 and 300 m.sup.2/g. The invention also provides a method for preparing a catalyst, including: 1) dissolving an organic salt of a transition metal in an organic solvent including a polyhydric alcohol, to yield a mixture; and 2) heating and stirring the mixture in the presence of air or inert gas, holding the mixture at the temperature of between 150 and 250° C. for between 30 and 240 min, to yield the catalyst.

A catalyst, including: a transition metal; and an organic solvent. The transition metal is dispersed in the organic solvent in the form of monodisperse nanoparticles; the transition metal has a grain size of between 1 and 100 nm; and the catalyst has a specific surface area of 5 and 300 m.sup.2/g. The invention also provides a method for preparing a catalyst, including: 1) dissolving an organic salt of a transition metal in an organic solvent including a polyhydric alcohol, to yield a mixture; and 2) heating and stirring the mixture in the presence of air or inert gas, holding the mixture at the temperature of between 150 and 250° C. for between 30 and 240 min, to yield the catalyst.

A self-assembling structure using non-equilibrium driving forces leading to “living crystals” and other maniputable particles with a complex dynamics. The dynamic self-assembly assembly results from a competition between self-propulsion of particles and an attractive interaction between the particles. As a result of non-equilibrium driving forces, the crystals form, grow, collide, anneal, repair themselves and spontaneously self-destruct, thereby enabling reconfiguration and assembly to achieve a desired property.

A self-assembling structure using non-equilibrium driving forces leading to “living crystals” and other maniputable particles with a complex dynamics. The dynamic self-assembly assembly results from a competition between self-propulsion of particles and an attractive interaction between the particles. As a result of non-equilibrium driving forces, the crystals form, grow, collide, anneal, repair themselves and spontaneously self-destruct, thereby enabling reconfiguration and assembly to achieve a desired property.

A honeycomb structure includes a pillar-shaped honeycomb structure body including porous partition walls defining and forming a plurality of cells which extend from an inflow end face to an outflow end face, and a porous outer wall surrounding the partition walls, a porous supporting bulge disposed to extend out from a circumference of the outer wall so that at least a part of the outer wall is exposed, and plugging portions arranged in open ends of the cells, and the supporting bulge has support portions and a side wall portion, and the partition walls and the outer wall of the honeycomb structure body and the support portions and the side wall portion of the supporting bulge are all formed monolithically by formation of a ceramic raw material.

A honeycomb structure includes a pillar-shaped honeycomb structure body including porous partition walls defining and forming a plurality of cells which extend from an inflow end face to an outflow end face, and a porous outer wall surrounding the partition walls, a porous supporting bulge disposed to extend out from a circumference of the outer wall so that at least a part of the outer wall is exposed, and plugging portions arranged in open ends of the cells, and the supporting bulge has support portions and a side wall portion, and the partition walls and the outer wall of the honeycomb structure body and the support portions and the side wall portion of the supporting bulge are all formed monolithically by formation of a ceramic raw material.

The invention relates to a method for producing iron-containing shaped catalyst bodies by means of 3D printing technology and to iron-containing shaped catalyst bodies that are obtainable by this method and to their use as catalysts in the ammonia synthesis or the Fischer-Tropsch reaction.

The invention relates to a method for producing iron-containing shaped catalyst bodies by means of 3D printing technology and to iron-containing shaped catalyst bodies that are obtainable by this method and to their use as catalysts in the ammonia synthesis or the Fischer-Tropsch reaction.

In accordance with the present subject matter there is provided a process for producing mono-, di- and triesters of glycerol over a catalyst composition. The catalyst composition including a base catalyst and a support material based on phyllosilicates of montmorillonite structure and the process for preparing the catalyst composition is also described.