Patent classifications
B01J23/04
HYDROCARBON ADSORPTION MATERIAL, EXHAUST GAS CLEANING CATALYST, AND EXHAUST GAS CLEANING SYSTEM
Provided are a hydrocarbon adsorbent, an exhaust gas purifying catalyst, and an exhaust gas purifying system, which are capable of adsorbing hydrocarbons, storing the adsorbed hydrocarbons up to a relatively high temperature, and desorbing the adsorbed and stored hydrocarbons at a relatively high temperature.
The hydrocarbon adsorbent contains a multipore zeolite containing, outside the zeolite framework, at least one metal selected from the group consisting of transition metals belonging to Groups 3 to 12 in the periodic table, amphoteric metals belonging to Groups 13 and 14 in the periodic table, alkali metals, and alkaline earth metals; and has a content ratio of the metal of 9% by mass or less relative to the multipore zeolite containing the metal.
Catalytic hydrocarbon dehydrogenation
A catalyst for dehydrogenation of hydrocarbons includes a support including zirconium oxide and alumina. A concentration of the zirconium oxide in the catalyst is in a range of from 1 weight percent (wt. %) to 20 wt. %. The catalyst includes from 0.01 wt. % to 2 wt. % of an alkali metal or alkaline earth metal. The catalyst includes from 1 wt. % to 2 wt. % of tin. The catalyst includes from 0.1 wt. % to 2 wt. % of a platinum group metal. The alkali metal or alkaline earth metal, tin, and platinum group metal are disposed on the support.
Catalytic hydrocarbon dehydrogenation
A catalyst for dehydrogenation of hydrocarbons includes a support including zirconium oxide and alumina. A concentration of the zirconium oxide in the catalyst is in a range of from 1 weight percent (wt. %) to 20 wt. %. The catalyst includes from 0.01 wt. % to 2 wt. % of an alkali metal or alkaline earth metal. The catalyst includes from 1 wt. % to 2 wt. % of tin. The catalyst includes from 0.1 wt. % to 2 wt. % of a platinum group metal. The alkali metal or alkaline earth metal, tin, and platinum group metal are disposed on the support.
GLASS FIBER FILTER ELEMENT FOR VISIBLE LIGHT PHOTOCATALYSIS AND AIR PURIFICATION AND PREPARATION METHOD THEREOF
A glass fiber filter element for visible light photocatalysis and air purification and a method for preparing the same. The glass fiber filter element includes 4 to 7 wt % of nanoparticles including at least one selected from zinc oxide, graphene oxide, titanium oxide, and reduced graphene oxide, 2 to 7 wt % of silver nanowires, 3 to 12 wt % of an adhesive system, and 78 to 91 wt % of a glass fiber mat, based on the total weight of the glass fiber filter element. The glass fiber mat is made of at least two glass fibers with different diameters, and the diameters are in a range of 0.15 to 3.5 μm. The nanoparticles have a particle size from 1 to 200 nm, and the silver nanowires have a diameter of 15 to 50 nm.
GLASS FIBER FILTER ELEMENT FOR VISIBLE LIGHT PHOTOCATALYSIS AND AIR PURIFICATION AND PREPARATION METHOD THEREOF
A glass fiber filter element for visible light photocatalysis and air purification and a method for preparing the same. The glass fiber filter element includes 4 to 7 wt % of nanoparticles including at least one selected from zinc oxide, graphene oxide, titanium oxide, and reduced graphene oxide, 2 to 7 wt % of silver nanowires, 3 to 12 wt % of an adhesive system, and 78 to 91 wt % of a glass fiber mat, based on the total weight of the glass fiber filter element. The glass fiber mat is made of at least two glass fibers with different diameters, and the diameters are in a range of 0.15 to 3.5 μm. The nanoparticles have a particle size from 1 to 200 nm, and the silver nanowires have a diameter of 15 to 50 nm.
Catalyst particle shape
A catalytic system is provided which comprises a tubular reactor and at least one catalyst particle located within the tubular reactor. The catalyst particles have a particular geometric form which promotes heat transfer with the tubular reactor. Certain specific catalyst particles are also provided.
RHEOLOGY-MODIFYING DIFUNCTIONAL COMPOUND
A difunctional compound T prepared by reacting one molar equivalent of at least one dihalogenated compound (a), and two molar equivalents of a same polyalkoxylated compound (b) selected from the group consisting of straight aliphatic monoalcohols (b1), branched aliphatic monoalcohols (b2), cycloaliphatic monoalcohols (b3), monoaromatic monoalcohols (b4), and polyaromatic monoalcohols (b5).
Heterogeneous catalyst for transesterification and method of preparing same
A transesterification catalyst that is heterogeneous and a method for preparing said transesterification catalyst are provided. The catalyst can be used in a variety of transesterification reactor configurations including CSTR (continuous stirred tank reactors), ebullated (or ebullating) beds or any other fluidized bed reactors, and PFR (plug flow, fixed bed reactors). The catalyst can be used for manufacturing commercial grade biodiesel, biolubricants and glycerin.
Heterogeneous catalyst for transesterification and method of preparing same
A transesterification catalyst that is heterogeneous and a method for preparing said transesterification catalyst are provided. The catalyst can be used in a variety of transesterification reactor configurations including CSTR (continuous stirred tank reactors), ebullated (or ebullating) beds or any other fluidized bed reactors, and PFR (plug flow, fixed bed reactors). The catalyst can be used for manufacturing commercial grade biodiesel, biolubricants and glycerin.
Method for Co-Producing Synthetical Rutile and Polymeric Ferric Sulfate with Waste Sulfuric Acid
The present disclosure discloses a method for co-producing synthetical rutile and polymeric ferric sulfate with waste sulfuric acid, which includes the following steps of: S1, performing deep reduction on ilmenite to obtain reduced ilmenite with a metallization rate of 85% or more; S2, leaching the reduced ilmenite with waste sulfuric acid; S3, performing solid-liquid separation on a mixed solution after the leaching in step S2, and drying a solid to obtain synthetical rutile, wherein a filtrate is a ferrous sulfate solution; and then performing step S4 or S5 to obtain a polymeric ferric sulfate finished product. The waste sulfuric acid is adopted in the present disclosure to leach the reduced ilmenite to prepare the synthetical rutile, a novel waste acid recycling mode is formed