A method of cleaning spent catalyst material from a catalyst filter basket. The catalyst filter basket includes a central frame having a base ring and a generally cylindrical inner screen portion which extends upwardly from the base ring. A generally cylindrical outer screen assembly is releasably secured to the central frame by a quick release mechanism.

Provided is a ceramic composite material and a wavelength converter. The ceramic composite material includes: an alumina matrix, a fluorescent powder uniformly distributed in the alumina matrix, and scattering centers uniformly distributed in the alumina matrix, wherein the alumina matrix is an alumina ceramics, the scattering centers are alumina particles, the alumina particles each have a particle diameter of 1 μm to 10 μm, and the fluorescent powder has a particle diameter of 13 μm to 20 μm.

This disclosure describes an improved heat transfer system for use in reaction vessels used in chemical and biological processes. In one embodiment, a heat transfer baffle comprising two sub-assemblies adjoined to one another is provided.

The invention relates to a device for the upflow of a single-phase fluid comprising at least two beds of solid particles and at least one bypass means for a portion of said fluid, and also to the use thereof.

A catalytic bed for the partial oxidation of n-butane to maleic anhydride which comprises at least one first catalytic layer and at least one second catalytic layer, wherein each catalytic layer consists of a vanadium and phosphorus mixed oxide (VPO) catalyst and only the catalyst of the second catalytic layer further comprises tungsten, and wherein the second catalytic layer constitutes 25% to 45% of the total length of the catalytic bed and is arranged consecutively after the first catalytic layer along the direction in which the mixture of gases comprising the oxidation reagents flows. The present invention also relates to a process for producing maleic anhydride by partial oxidation of n-butane which uses the catalytic bed.

The present invention relates to a triphasic single reactor comprising a solid, a liquid and a gaseous component, wherein the (i) the solid component is (a) a catalytically active composite based on (b) at least one perforated and permeable support, wherein the catalytically active composite is on at least one side of the support and inside the support and (a) the catalytically active composite is obtained by applying a suspension comprising at least one inorganic component of a compound of at least one of the elements Ce, La Sc, Y, Ti, Zr, Hf, Rf, V, Nb, Ta, Db, Cr, Mo, W, Sg, Mn, Tc, Re, Bh, Fe, Co, B, Al, In, Tl, Si, Ge, Sn, Pb, Sb and Bi with at least one of the elements Te, Se, S, O, Sb, As, P, N, Ge, Si, C and Ga and/or a compound of one of the elements Ti, Zr, Al, Ce and Si with oxygen, and/or a metal selected from Pt, Rh, Ru, Ir, Cu, Ni, Co, Mg, Zn, Al and Pd, in suspension in a sol, and (b) the support comprises fibers of at least one material selected from the group consisting of carbon, metal, alloy, ceramic, glass, mineral, plastic, amorphous substance, composite, natural product, and a combination thereof and heating the support at least once to a temperature of between 100 to 800° C. for 10 minutes to 5 hours, during which the suspension comprising the inorganic component is solidified on and inside the support.

A process for increasing the productivity of equilibrium-restricted reactions and for increasing the productivity of a target compound includes the steps of (a) providing a reaction mixture comprising reactants; (b) subjecting the reaction mixture to the equilibrium reaction in a reactor or sequence of reactors, to obtain a reactor outlet mixture comprising the target compound and at least one of the reactants; (c) regenerating the loaded sorbent obtained in step (e), by flushing the loaded sorbent with the reactor outlet mixture originating from step (b), to obtain regenerated sorbent and an effluent comprising desorbed product; (d) separating the effluent originating from step (c) into a product stream and a reactant stream; and (e) a sorption step to obtain a loaded sorbent and a depleted mixture.

The machinery and methods disclosed herein are based on the use of a specialized extruder configured to continuously convey and plasticize/moltenize selected lignocellulosic biomass and/or waste plastic materials into a novel variable volume tubular reactor, wherein the plasticized/moltenized material undergoes reaction with circumferentially injected supercritical water—thereby yielding valuable simple sugar solutions and/or liquid hydrocarbon mixtures (e.g., “neodiesel”), both of which are key chemical commodity products. The reaction time may be adjusted by changing the reactor volume. The machinery includes four zones: (1) a feedstock conveyance and plasticization/moltenization zone; (2) a steam generation and manifold distribution zone; (3) a central supercritical water reaction zone; and (4) a pressure let-down and reaction product separation zone. The machinery and methods minimize water usage—thereby enabling the economic utilization of abundant biomass and waste plastics as viable renewable feedstocks for subsequent conversion into alternative liquid transportation fuels and valuable green-chemical products.

The present specification relates to a method comprising: (A) mixing a ferrite-based catalyst molded article with diluent material particles; and (B) adding the mixture to a catalyst reactor, and a method for preparing butadiene using the same.

Proposed is a carbon dioxide reforming (CDR) reactor having a multilayered catalyst layer arrangement for preventing catalyst deactivation, wherein, in the reactor in which a CDR reaction for reacting methane (CH.sub.4) with carbon dioxide (CO.sub.2) to reform the methane into a synthesis gas including carbon monoxide (CO) and hydrogen (H.sub.2) is performed, in order to prevent a case where an endothermic reaction between a catalyst and heated reactant gas supplied to the reactor gradually causes the temperature of the reactant gas to decrease and the catalyst is deactivated by cokes generated due to the decrease in temperature of the reactant gas, CDR catalysts in the reactor are arranged in multiple layers in a multilayered structure to allow the reactant gas temperature that has decreased due to the endothermic reaction to be restored in spaces between the catalyst layers.