Method for manufacturing of spheroidal alumina particles
US-9669387-B2 · Jun 6, 2017 · US
US10022702B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10022702-B2 |
| Application number | US-201615148109-A |
| Country | US |
| Kind code | B2 |
| Filing date | May 6, 2016 |
| Priority date | May 7, 2015 |
| Publication date | Jul 17, 2018 |
| Grant date | Jul 17, 2018 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
The invention also concerns processes for the preparation of said particles as well as catalysts comprising said particles as a support, and their use in catalytic hydrocarbon treatment processes, in particular in a catalytic reforming process.
Opening claim text (preview).
The invention claimed is: 1. Spheroidal alumina particles having a BET specific surface area of 150 to 300 m 2 /g, a mean particle diameter 1.2 to 3 mm and a particle diameter dispersion, expressed as the standard deviation, not exceeding 0.1, a total pore volume, measured by mercury porosimetry, of 0.50 to 0.85 mL/g, a degree of macroporosity within a particle of less than 30%, and a dispersion of the diameters of macropores, expressed as a ratio D90/D50, not exceeding 8. 2. The spheroidal alumina particles according to claim 1 , having a value for settled packing density of 0.4 to 0.8 g/mL. 3. The spheroidal alumina particles according to claim 1 , having a mean grain crushing strength value of at least 25 N. 4. The spheroidal alumina particles according to claim 1 , in which the total pore volume, measured by mercury porosimetry, is 0.60 to 0.85 mL/g. 5. The spheroidal alumina particles according to claim 1 , in which the dispersion of the diameters of the macropores, expressed as D90/D50, does not exceed 6. 6. A process for the production of spheroidal alumina particles according to claim 1 , comprising: a) preparing a suspension comprising water, an acid and at least one boehmite powder, b) adding a solid pore-forming agent having a particle size in the range 0.05 to 30 μm to the suspension obtained in a), c) mixing the suspension obtained in b) until the viscosity of said mixture is in the range 200 to 700 mPa·s, d) shaping the spheroidal particles by drop coagulation using the mixture obtained in step c), e) drying the particles obtained in d), f) calcining the particles obtained in e). 7. The process according to claim 6 , in which the solid pore-forming agent is starch, flour latex, polystyrene or acrylic particles, a polysaccharide, carbon black particles or sawdust. 8. The process according to claim 6 , in which the proportion of solid pore-forming agent, expressed as the ratio of the mass of the pore-forming agent with respect to the total mass of oxides, is in the range 0.2% to 50% by weight. 9. A process for the production of spheroidal alumina particles having a BET specific surface area of 150 to 300 m 2 /g, a mean particle diameter 1.2 to 3 mm and a particle diameter dispersion, expressed as the standard deviation, not exceeding 0.1, a total pore volume, measured by mercury porosimetry, of 0.50 to 0.85 mL/g, a degree of macroporosity within a particle of less than 30%, and a dispersion of the diameters of macropores, expressed as the ratio D90/D50, not exceeding 8, comprising: a) preparing a suspension comprising water, an acid and at least one boehmite powder, b′) adding at least one liquid pore-forming agent, at least one surfactant and optionally water, or an emulsion comprising at least one liquid pore-forming agent, at least one surfactant and water, to the suspension obtained in a), b″) dispersing the suspension obtained in b′) with a disperser functioning at a shear rate in the range 1000 to 200000 s −1 , c) mixing the suspension dispersed in b″) until the viscosity of said mixture is in the range 200 to 700 mPa·s, d) shaping the spheroidal particles by drop coagulation using the mixture obtained in step c), e) drying the particles obtained in d), f) calcining the particles obtained in e). 10. The process according to claim 9 , in which the liquid pore-forming agent is a grease, oil, mineral wax, fat, hydrocarbon or oil cut and the surfactant is a non-ionic or ionic surfactant. 11. The process according to claim 9 , in which the proportion of the liquid pore-forming agent, expressed as the ratio of the mass of liquid pore-forming agent to the total mass of oxides, is in the range 0.2% to 50% by weight and in which the proportion of surfactant, defined as being equal to the ratio of the mass of surfactant to the mass of pore-forming agent, is in the range 1% to 25% by weight. 12. The process according to claim 9 , in which at least one solid pore-forming agent with a particle size in the range 0.05 to 30 μm is added to the suspension of b′). 13. A process for the preparation of spherical alumina particles having a BET specific surface area of 150 to 300 m 2 /g, a mean particle diameter 1.2 to 3 mm and a particle diameter dispersion, expressed as the standard deviation, not exceeding 0.1, a total pore volume, measured by mercury porosimetry, of 0.50 to 0.85 mL/g, a degree of macroporosity within a particle of less than 30%, and a dispersion of the diameters of macropores, expressed as D90/D50, not exceeding 8 comprising: a) preparing a suspension comprising water, an acid and at least one boehmite powder, b) adding a solid pore-forming agent having a particle size in the range 0.05 to 30 μm to the suspension obtained in a), c) mixing the suspension obtained in b) until the viscosity of said mixture is in the range 200 to 700 mPa·s, d) shaping the spheroidal particles by drop coagulation using the mixture obtained in c), e) drying the particles obtained in d), f) calcining the particles obtained in (e), in which the suspension of a) further comprises a charge of alumina or alumina precursor constituted by particles with a volumetric median diameter of 50 μm or less. 14. A catalyst comprising a support formed by particles according to claim 1 and one or more noble metals of group VIII of the periodic table. 15. The catalyst according to claim 14 , further comprising one or more elements of groups IA, IIA, IIIA, IVA, VA of the periodic table or fluorine, chlorine, bromine or iodine. 16. A catalytic reforming reaction, comprising subjecting a hydrocarbon feed to reforming conditions, in the presence of a catalyst according to claim 14 .
by wet processes · CPC title
Addition of a binding agent or of material, later completely removed among others as result of heat treatment, leaching or washing,(e.g. forming of pores; protective layer, desintegrating by heat) · CPC title
of the platinum group metals · CPC title
characterised by the catalyst · CPC title
Aluminium oxide; Aluminium hydroxide; Aluminates · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.