Production of acrylic acid
US-2015353466-A1 · Dec 10, 2015 · US
US2016264505A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2016264505-A1 |
| Application number | US-201615067211-A |
| Country | US |
| Kind code | A1 |
| Filing date | Mar 11, 2016 |
| Priority date | Mar 13, 2015 |
| Publication date | Sep 15, 2016 |
| Grant date | — |
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Bicomponent catalysts and methods for making bio-based acrylic acid, acrylic acid derivatives, or mixtures thereof from lactic acid, lactic acid derivatives, or mixtures thereof are provided.
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What is claimed is: 1 . A method of making acrylic acid, acrylic acid derivatives, or mixtures thereof comprising contacting a stream comprising lactic acid, lactic acid derivatives, or mixtures thereof with a bicomponent catalyst comprising an HO-Re(VII)=O moiety and a compound having an oxophilic metal. 2 . The method of claim 1 , wherein said HO-Re(VII)=O moiety comprises perrhenic acid. 3 . The method of claim 1 , wherein said oxophilic metal is selected from the group consisting of Mg, Ca, Sr, Ba, Y, Ti, Zr, Hf, V, Nb, Ta, Cr, Mo, and W. 4 . The method of claim 1 , wherein said compound having an oxophilic metal is selected from the group consisting of oxophilic metal phosphate, oxophilic metal sulfate, oxophilic metal oxide, and mixtures thereof. 5 . The method of claim 4 , wherein said oxophilic metal phosphate is selected from the group consisting of M 2 P 2 O 7 , M 3 (PO 4 ) 2, MHPO 4 , M(H 2 PO 4 ) 2 , and mixtures thereof; and wherein M is selected from the group consisting of Be, Mg, Ca, Sr, Ba, and mixtures thereof. 6 . The method of claim 4 , wherein said oxophilic metal oxide is selected from the group consisting of Nb 2 O 5 , LiONbO 2 , Ta 2 O 5 , and mixtures thereof. 7 . The method of claim 1 , wherein said contacting is carried out at a temperature between about 180° C. and about 250° C. 8 . The method of claim 7 , wherein said temperature is about 200° C. 9 . The method of claim 1 , wherein said stream is gaseous. 10 . The method of claim 1 , wherein said stream is liquid. 11 . The method of claim 1 , wherein the conversion of said lactic acid, lactic acid derivatives, or mixtures thereof is at least about 50 mol %. 12 . The method of claim 11 , wherein said conversion is at least about 80 mol %. 13 . The method of claim 12 , wherein said conversion is at least about 90 mol %. 14 . The method of claim 1 , wherein the selectivity of said acrylic acid, acrylic acid derivatives, or mixtures thereof is at least about 50 mol %. 15 . The method of claim 14 , wherein said selectivity is at least about 80 mol %. 16 . The method of claim 15 , wherein said selectivity is at least about 90 mol %.
by splitting-off hydrogen or functional groups; by hydrogenolysis of functional groups {(C07C51/36 - C07C51/373 take precedence)} · CPC title
Vanadium, niobium or tantalum · CPC title
Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 (B01J21/16 takes precedence) · CPC title
by reactions not involving formation of carboxyl groups · CPC title
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