C07C2529/04

Molecular sieve SCM-14, a preparation process and use thereof

The invention relates to a molecular sieve SCM-14, a preparation process and use thereof. The molecular sieve has a schematic chemical composition of a formula of “SiO.sub.2.1/nGeO.sub.2” or a formula of “kF.mQ.SiO.sub.2.1/nGeO.sub.2.pH.sub.2O”, wherein the molar ratio of silicon to germanium, n, satisfies n≤30, and other values and symbols are defined in the specification. The molecular sieve has unique XRD diffraction data and can be used as an adsorbent or a catalyst.

MOLECULAR SIEVE SSZ-116, ITS SYNTHESIS AND USE
20210220807 · 2021-07-22 ·

A novel synthetic crystalline aluminogermanosilicate molecular sieve material, designated SSZ-116, is provided. SSZ-116 can be synthesized using 3-[(3,5-di-tert-butylphenyl)methyl]-1,2-dimethyl-1H-imidazolium cations as a structure directing agent. SSZ-116 may be used in organic compound conversion reactions and/or sorptive processes.

AROMATIZATION CATALYST WITH IMPROVED ISOMERIZATION, PROCESS OF MAKING AND USING THEREOF

Disclosed is a catalyst comprising a zeolite comprising a framework, the framework comprising silicon and aluminum, and a noble metal. The zeolite has undergone at least a first exchange with a Group I or II cation or ammonium and thereafter is contacted with a second Group I or II cation. The step of contacting comprises an exchange, incipient wetness, or dry impregnation. The noble metal is deposited at the zeolite.

Molecular sieve SCM-15, synthesis method therefor and use thereof

The invention relates to a molecular sieve SCM-15, a preparation process and use thereof. The molecular sieve comprises a schematic chemical composition of a formula of “SiO.sub.2.GeO.sub.2”, wherein the molar ratio of silicon and germanium satisfies SiO.sub.2/GeO.sub.2≥1. The molecular sieve has unique XRD diffraction data and can be used as an adsorbent or a catalyst.

MULTISTAGE ALKYLATION VIA BYPRODUCT REMOVAL

The present disclosure is related to processes for the alkylation of an isoparaffin. The process may include introducing, in a multistage reactor, a solid acid catalyst including a zeolite to an isoparaffin feed and an olefin feed to form an alkylation product mixture including C5+ olefins. The processes may further include separating at least a portion of the C5+ olefins from the alkylation product mixture to form an oligomer light stream. The present disclosure further relates to multistage reactors for the alkylation of an isoparaffin with an olefin. The multistage reactors may include a plurality of stages, and a plurality of separation systems. The multistage reactors may also include an outlet space coupling each stage to a separation system and an inlet space coupling a separation system to a subsequent stage.

Processes of forming metal-doped zeolite catalysts with enhanced mesoporosity

According to embodiments, a process of forming a catalyst for aromatizing hydrocarbons may include enhancing a mesoporosity of a zeolite support by a base-leaching treatment, an acid-leaching treatment, or both to form a zeolite support having enhanced mesoporosity, mixing the zeolite support having enhanced mesoporosity with a solution containing zinc or gallium to disperse the zinc or gallium on the zeolite support having enhanced mesoporosity, and calcining the zeolite support having enhanced mesoporosity with zinc or gallium dispersed thereon to form a zinc- or gallium-doped zeolite catalyst having a mesopore volume of greater than 0.09 cm.sup.3/g and less than 0.20 cm.sup.3/g.

Method and system for producing aromatic hydrocarbons from a renewable resource

Disclosed are a method and a system for producing bio-derived aromatic hydrocarbons from a renewable resource. More particularly, the disclosure provides for the co-location of a biomass reactor unit and an aromatization reactor unit to produce benzene from a renewable source such as plant mass. Hexane produced from cellulose in the biomass reactor unit can be converted to benzene in the aromatization reactor unit and hydrogen produced in the aromatization reactor unit can be used in the biomass reactor unit. Also described is the use of a mixture of bio-derived hexane produced from cellulose and naphtha in an aromatization process.

MOLECULAR SIEVE SCM-15, SYNTHESIS METHOD THEREFOR AND USE THEREOF
20200188891 · 2020-06-18 ·

The invention relates to a molecular sieve SCM-15, a preparation process and use thereof. The molecular sieve comprises a schematic chemical composition of a formula of SiO.sub.2.GeO.sub.2, wherein the molar ratio of silicon and germanium satisfies SiO.sub.2/GeO.sub.21. The molecular sieve has unique XRD diffraction data and can be used as an adsorbent or a catalyst.

MOLECULAR SIEVE SCM-14, A PREPARATION PROCESS AND USE THEREOF
20200188892 · 2020-06-18 ·

The invention relates to a molecular sieve SCM-14, a preparation process and use thereof. The molecular sieve has a schematic chemical composition of a formula of SiO.sub.2.1/nGeO.sub.2 or a formula of kF.mQ.SiO.sub.2.1/nGeO.sub.2.pH.sub.2O, wherein the molar ratio of silicon to germanium, n, satisfies n30, and other values and symbols are defined in the specification. The molecular sieve has unique XRD diffraction data and can be used as an adsorbent or a catalyst.

SUPPORTED CORE-SHELL BIMETALLIC CATALYST WITH HIGH SELECTIVITY FOR PROPANE DEHYDROGENATION
20200122122 · 2020-04-23 · ·

A supported core-shell bimetallic catalyst with high selectivity for propane dehydrogenation, containing platinum (Pt) as active species, 3d transition metals (Fe, Co and Ni) as promoters and SBA-15 as support. The addition of 3d metals and the formation of Pt3d alloys in subsurface result in a core-shell bimetallic catalyst which promotes the propene selectivity by decreasing the d-band center of surface Pt atoms and facilitating the desorption of propene on Pt. In another aspect, the reduced usage of Pt is achieved with the addition of 3d transition metals as well as the increased utilization of Pt atoms. The catalyst can be effectively used as a catalyst for the preparation of propene by propane dehydrogenation and 85% of propene selectivity can be achieved in propane dehydrogenation.