Oxide materials and synthesis by fluoride/chloride anion promoted exfoliation
US-9522390-B2 · Dec 20, 2016 · US
US9446390B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9446390-B2 |
| Application number | US-201514724204-A |
| Country | US |
| Kind code | B2 |
| Filing date | May 28, 2015 |
| Priority date | May 30, 2014 |
| Publication date | Sep 20, 2016 |
| Grant date | Sep 20, 2016 |
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 present invention relates to a process for preparing acrylic acid comprising (i) providing a stream comprising a formaldehyde source and acetic acid and (ii) contacting this stream with an aldol condensation catalyst comprising a zeolitic material, wherein the framework structure of the zeolitic material in (ii) includes Si and O, and has a molar Al:Si ratio of 0:1 to 0.001:1, and wherein the framework structure of the zeolitic material in (ii), in addition to Si and any Al, comprises one or more elements selected from the group consisting of tetravalent elements Y other than Si and trivalent elements X other than Al.
Opening claim text (preview).
The invention claimed is: 1. A process for preparing acrylic acid, the process comprising contacting a stream S 4 comprising a formaldehyde source and acetic acid with an aldol condensation catalyst comprising a zeolitic material to obtain a stream S 6 comprising acrylic acid; wherein a framework structure of the zeolitic material comprises Si, O, and optionally Al, and one or more elements selected from the group consisting of a tetravalent element Y other than Si and a trivalent element X other than Al; and the framework structure of the zeolitic material has a molar Al:Si ratio of from 0:1 to 0.001:1. 2. The process according to claim 1 , wherein the framework structure of the zeolitic material comprises YO 2 where Y is optionally selected from the group consisting of Sn, Ti, Zr, Ge, V and any combination thereof. 3. The process according to claim 1 , wherein the framework structure of the zeolitic material comprises X 2 O 3 where X is optionally selected from the group consisting of B, In, Ga, Fe, Ta and any combination thereof. 4. The process according to claim 1 , wherein zeolitic material comprises one or more non-framework elements Z selected from the group consisting of Ti, Zr, V, Nb, Ta, Cr, Mo, W, Mn, Fe, Co, Ni, Zn, Ga, Ge, In, Sn, Pb, P, N and S. 5. The process according to claim 1 , wherein the zeolitic material has a structure selected from the group consisting of BEA, MFI, MWW, FAU, MOR, CHA, LEV, FER, MEL, MOR, AFI, RRO, CDO and any combination thereof. 6. The process according to claim 1 , wherein the zeolitic material has a structure of BEA and optionally has a molar (Si+Y):X ratio of from 2:1 to 500:1. 7. The process according to claim 1 , wherein the zeolitic material has a structure of MEI, MEL, or any combination thereof and optionally has a molar (Si+Y):X ratio of from 2:1 to 500:1. 8. The process according to claim 1 , wherein the zeolitic material has a structure of MWW, optionally has a molar (Si+Y):X ratio of from 2:1 to 500:1, and optionally comprises Zn as a non-framework element. 9. The process according to claim 1 , wherein a total content of alkali metal and alkaline earth metal in the zeolitic material, calculated as alkali metal oxide (M 2 O) and alkaline earth metal oxide (MO), is from 0% to 0.1% by weight, based on a total weight of the zeolitic material. 10. The process according to claim 1 , wherein the aldol condensation catalyst further comprises a binder material which is optionally selected from the group consisting of graphite, SiO 2 ,TiO 2 , ZrO 2 , MgO, any combination thereof and a mixed oxide of at least two elements selected from the group consisting of Si, Ti, Zr, Mg and any combination thereof. 11. The process according to claim 1 , wherein the aldol condensation catalyst is in a form of shaped bodies, in a star shape, in a tablet form, in a form of spheres, or in a form of hollow cylinders. 12. The process according to claim 1 , wherein a molar ratio of acetic acid to formaldehyde, obtained and/or obtainable from the formaldehyde source, in the stream S 4 ranges from 0.01:1 to 10:1, and the stream S 4 optionally further comprises one or more diluents which optionally are selected from the group consisting of nitrogen, carbon monoxide, carbon dioxide, ethene, acetone, water, and any combination thereof. 13. The process according to claim 1 , wherein the contacting is effected at a temperature of from 200 to 400° C., the stream S 4 prior to the contacting is optionally brought to a temperature of from 150 to 250° C., the contacting is effected at a pressure of from 0.01 to 10 bar, and the contacting is effected at a space velocity (GHSV) of from 50 to 10 000 h −1 . 14. The process according to claim 1 , wherein a space-time yield of the contacting ranges from 0.01 to 2.5 kg/kg/h, and the space-time yield is defined as kg(acrylic acid)/kg(aldol condensation cataltyst)/h. 15. The process according to claim 1 , further comprising regenerating the aldol condensation catalyst optionally at a temperature of from 300 to 700° C. and optionally in the presence of oxygen. 16. The process according to claim 1 , wherein the formaldehyde source is an anhydrous formaldehyde source. 17. The process according to claim 1 , wherein a temperature-programmed desorption with NH 3 (NH3TPD) of the zeolitic material has a desorption spectrum with a desorption maximum within at least one of temperature ranges of from 0 to 250° C., from 251 to 500° C., and from 501 to 700° C., and following deconvolution of the desorption spectrum, the desorption maximum in the temperature range of 0 to 250° C. has a concentration of desorbed NH 3 of from 0.001 to 1.0 mmol/g, the desorption maximum in the temperature range of 251 to 500° C. has a concentration of desorbed NH 3 of from 0.001 to 0.5 mmol/g, and the desorption maximum in the temperature range 501 to 700° C. has a concentration of desorbed NH 3 of from 0.001 to 0.1 mmol/g, where the concentration of desorbed NH 3 is defined as mmol(desorbed NH 3 )/g(zeolitic material). 18. The process according to claim 1 , wherein the aldol condensation catalyst further comprises from 0% to 1% by weight of vanadium, calculated as vanadium oxide and based on a total weight of the aldol condensation catalyst.
MWW-type, e.g. MCM-22, ERB-1, ITQ-1, PSH-3 or SSZ-25 · CPC title
by isomerisation; by change of size of the carbon skeleton · CPC title
MWW-type, e.g. MCM-22, ERB-1, ITQ-1, PSH-3 or SSZ-25 · CPC title
containing rare earth elements, titanium, zirconium, hafnium, zinc, cadmium, mercury, gallium, indium, thallium, tin or lead · CPC title
Zeolite Beta · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.