The present invention describes the process of preparing ceramics for the absorption of ACIDIC gases, which worsen the greenhouse effect, that are released in combustion systems, or that are present in closed environments. In relation to carbon dioxide, principal target of the present invention, the process of absorption, transport, processing and transformation of the gas into other products is described. The process uses ceramic materials prepared through the solid mixture of one or more metallic oxides, with one or more binding agents and an expanding agent. The product generated can be processed and the absorbent system regenerated. The carbon dioxide obtained in the processing can be used as analytic or commercial carbonic gas, various carbamates and ammonium carbonate.

A commercially available anatase titania catalyst is shown to be catalytically active towards the formation of methacrolein from formaldehyde and propionaldehyde with conversions and selectivities close to 90%. This titania catalyst is readily available, non-toxic, and can be used with formaldehyde and a variety of other aldehyde compounds to make α,β-unsaturated aldehyde compounds. This process benefits from low raw material costs and is economically advantaged due to the elimination of catalyst separation. An additional advantage of this method involves the ability of the catalyst to be fully regenerated after a calcination step at 450° C. in air. This process shows promising stability and selectivity during lifetime studies, particularly when performed in the presence of a hydrogen carrier gas.

One exemplary embodiment can be a process for fluid catalytic cracking. The process can include sending a first catalyst from a first riser reactor and a second catalyst from a second riser reactor to a regeneration vessel having a first stage and a second stage. The first catalyst may be sent to the first stage and the second catalyst may be sent to the second stage of the regeneration vessel. Generally, the first stage is positioned above the second stage.

One exemplary embodiment can be a process for fluid catalytic cracking. The process can include sending a first catalyst from a first riser reactor and a second catalyst from a second riser reactor to a regeneration vessel having a first stage and a second stage. The first catalyst may be sent to the first stage and the second catalyst may be sent to the second stage of the regeneration vessel. Generally, the first stage is positioned above the second stage.

The present invention provides a catalyst for producing a hydrocarbon from a syngas, including one of a cobalt metal and a combination of a cobalt metal and cobalt oxides; zirconium oxides; and a noble metal; supported by a catalyst support mainly composed of silica, wherein a content of impurities in the catalyst is less than or equal to 0.15 mass %; a producing method and regenerating method thereof; and a producing method of the hydrocarbon by using the catalyst.

The present invention provides a catalyst for producing a hydrocarbon from a syngas, including one of a cobalt metal and a combination of a cobalt metal and cobalt oxides; zirconium oxides; and a noble metal; supported by a catalyst support mainly composed of silica, wherein a content of impurities in the catalyst is less than or equal to 0.15 mass %; a producing method and regenerating method thereof; and a producing method of the hydrocarbon by using the catalyst.

The present invention provides a process for the preparation of a (hydro)(chloro)fluoroalkene by contacting a reagent stream comprising a hydrochlorofluoroalkane with a catalyst in a reactor to dehydrochlorinate at least a portion of the hydrochlorofluoroalkane to produce a product stream comprising the (hydro)(chloro)fluoroalkene and hydrogen chloride (NCI), wherein the catalyst is selected from the group consisting of metal oxide catalysts, metal halide catalysts, zero-valent metal catalysts, carbon-based catalysts and mixtures thereof, and wherein (i) the catalyst is chlorinated prior to contacting it with the reagent stream comprising the hydrochlorofluoroalkane; and/or (ii) the contacting step is carried out in the presence of a HCI co-feed.

It is an object to provide a regenerated denitration catalyst whose denitration performance is restored compared with a denitration catalyst before use, utilizing a spent denitration catalyst, and a method for manufacturing the same. In a regenerated denitration catalyst according to the present disclosure, a spent denitration catalyst including a first titanium oxide as a main component, and a second titanium oxide are mixed. The spent denitration catalyst is already used in a denitration reaction in which nitrogen oxides in a gas are decomposed into nitrogen and water using a reducing agent. The second titanium oxide has a larger specific surface area per unit weight than the first titanium oxide. A content of the second titanium oxide based on a total weight of the first titanium oxide and the second titanium oxide is preferably 10% by weight or more and 90% by weight or less.

Supplemental heat required to raise the temperature of a regenerated catalyst to the minimum required to promote the catalyzed reaction in an FCC unit is provided by introducing adsorbent material containing HPNA compounds and HPNA precursors with the coked catalyst into the FCC catalyst regeneration unit for combustion. The HPNA compounds and HPNA precursors can be adsorbed on either a carbonaceous adsorbent, such as activated carbon, that is completely combustible and generates no ash, or on fresh or coked FCC catalyst that is recovered from an HPNA adsorption column that has treated the bottoms from a hydrocracking unit to remove the HPNA compounds and their precursors.

Supplemental heat required to raise the temperature of a regenerated catalyst to the minimum required to promote the catalyzed reaction in an FCC unit is provided by introducing adsorbent material containing HPNA compounds and HPNA precursors with the coked catalyst into the FCC catalyst regeneration unit for combustion. The HPNA compounds and HPNA precursors can be adsorbed on either a carbonaceous adsorbent, such as activated carbon, that is completely combustible and generates no ash, or on fresh or coked FCC catalyst that is recovered from an HPNA adsorption column that has treated the bottoms from a hydrocracking unit to remove the HPNA compounds and their precursors.