Catalysts for the dehydration of hydroxypropionic acid and its derivatives

US11090639B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-11090639-B2
Application numberUS-202016871160-A
CountryUS
Kind codeB2
Filing dateMay 11, 2020
Priority dateAug 28, 2015
Publication dateAug 17, 2021
Grant dateAug 17, 2021

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  1. Title

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  5. First independent claim

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Abstract

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Hydroxypropionic acid, hydroxypropionic acid derivatives, or mixtures thereof are dehydrated using a catalyst and a method to produce bio-acrylic acid, acrylic acid derivatives, or mixtures thereof. A method to produce the dehydration catalyst is also provided.

First claim

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What is claimed is: 1. A catalyst for the dehydration of lactic acid to acrylic acid comprising one or more amorphous phosphate salts; wherein said one or more amorphous phosphate salts consist essentially of the group consisting of K + , Rb + , Cs + , and mixtures thereof, and one or more phosphate anions selected from the group represented by empirical formula (I): [H 2(1-x) PO (4-x) ] −   (I); wherein x is 1; and wherein said one or more amorphous phosphate salts of said catalyst are neutrally charged. 2. The catalyst of claim 1 , wherein said one or more amorphous phosphate salts is KH 2(1-x) PO (4-x) ; and wherein x is 1. 3. The dehydration catalyst of claim 1 , wherein said one or more amorphous phosphate salts are selected from the group represented by empirical formula (Ib): M w I N (1-w) I H 2(1-x) PO (4-x)   (Ib); wherein M I and N I are two different monovalent cations; wherein x is 1; and wherein w is any real number greater than 0 and less than 1. 4. The catalyst of claim 1 , further comprising amorphous silicon oxide (SiO 2 ); wherein said amorphous silicon oxide is substantially chemically inert to said one or more phosphate salts. 5. The catalyst of claim 1 , further comprising one or more oxysalts; wherein said oxysalts comprise one or more polyvalent cations, and one or more oxyanions; wherein said oxyanions are selected from the group represented by molecular formulae (II) and (III): [H (a-2b) S c O (4c-b) ] (2c-a)−   (II) [Ta 2d O (5d+e) ] 2e−   (III); wherein a and b are positive integers or zero; wherein c, d, and e are positive integers; wherein (a-2b) is equal to or greater than zero; wherein (2c-a) is greater than zero; wherein said one or more oxysalts are neutrally charged; and wherein said one or more oxysalts are substantially chemically inert to said one or more phosphate salts. 6. The catalyst of claim 5 , further comprising amorphous silicon oxide (SiO 2 ); wherein said amorphous silicon oxide is substantially chemically inert to said one or more phosphate salts. 7. The catalyst of claim 5 , wherein said one or more polyvalent cations are selected from the group consisting of the cations of the metals Be, Mg, Ca, Sr, Ba, Sc, Y, Ti, Zr, Hf, V, Nb, Ta, Cr, Mo, W, Mn, Re, Al, Ga, In, Tl, Si, Ge, Sn, Pb, Sb, Bi, La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu, and mixtures thereof. 8. The catalyst of claim 7 , wherein said one or more polyvalent cations are selected from the group consisting of the cations of the metals Mg, Ca, Sr, Ba, Y, Mn, Al, Er, and mixtures thereof. 9. The catalyst of claim 5 , wherein said one or more oxyanions are selected from the group represented by molecular formulae (IIa) to (IId), (IIIa) to (IIIg), and mixtures thereof: [SO 4 ] 2−   (IIa) [S 2 O 7 ] 2−   (IIb) [HSO 4 ] 1−   (IIc) [SO 4 ] 2− .HSO 4 ] −   (IId) [Ta 2 O 6 ] 2−   (IIIa) [Ta 2 O 7 ] 4−   (IIIb) [Ta 2 O 9 ] 8−   (IIIc) [Ta 2 O 10 ] 10−   (IIId) [Ta 2 O 11 ] 12−   (IIIe) [Ta 4 O 11 ] 2−   (IIIf) [Ta 4 O 15 ] 10−   (IIIg). 10. The dehydration catalyst of claim 9 , wherein said one or more oxyanions are selected from the group represented by molecular formulae (IIa), (IIIa), and mixtures thereof: [SO 4 ] 2−   (IIa) [Ta 2 O 6 ] 2−   (IIIa). 11. The catalyst of claim 5 , wherein said one or more oxysalts are selected from the group consisting of CaSO 4 , SrSO 4 , BaSO 4 , SrK 2 (SO 4 ) 2 , SrRb 2 (SO 4 ) 2 , Ca 2 K 2 (SO 4 ) 3 , Ca 2 Rb 2 (SO 4 ) 3 , Ca 2 Cs 2 (SO 4 ) 3 , CaTa 4 O 11 , SrTa 4 O 11 , BaTa 4 O 11 , MgTa 2 O 6 , CaTa 2 O 6 , SrTa 2 O 6 , BaTa 2 O 6 , Mg 2 Ta 2 O 7 , Ca 2 Ta 2 O 7 , Sr 2 Ta 2 O 7 , SrK 2 Ta 2 O 7 , Ba 2 Ta 2 O 7 , Ba 3 Ta 2 O 8 , Mg 4 Ta 2 O 9 , Ca 4 Ta 2 O 9 , Sr 4 Ta 2 O 9 , Ba 4 Ta 2 O 9 , Ca 5 Ta 2 O 10 , Ca 2 KTa 3 O 10 , Ca 2 RbTa 3 O 10 , Ca 2 CsTa 3 O 10 , Sr 2 KTa 3 O 10 , Sr 2 RbTa 3 O 10 , Sr 2 CsTa 3 O 10 , Mg 5 Ta 4 O 15 , Sr 5 Ta 4 O 15 , Ba 5 Ta 4 O 15 , Sr 2 KTa 5 O 15 , Ba 2 KTa 5 O 15 , Sr 6 Ta 2 O 11 , Ba 6 Ta 2 O 11 , any of their hydrated forms, and mixtures thereof. 12. The catalyst of claim 11 , wherein said one or more oxysalts are selected from the group consisting of CaSO 4 , CaTa 2 O 6 , SrSO 4 , SrTa 2 O 6 , BaSO 4 , BaTa 2 O 6 , any of their hydrated forms, and mixtures thereof. 13. The catalyst of claim 5 , wherein said one or more amorphous phosphate salts are selected from the group consisting of KH 2(1-x) PO (4-x) , NaH 2(1-x) PO (4-x) , RbH 2(1-x) PO (4-x) , CsH 2(1-x) PO (4-x) , any of their hydrated forms, and mixtures thereof; wherein x is 1; and wherein said one or more oxysalts are selected from the group consisting of CaSO 4 , CaTa 2 O 6 , SrSO 4 , SrTa 2 O 6 , BaSO 4 , BaTa 2 O 6 , any of their hydrated forms, and mixtures thereof. 14. The catalyst of claim 13 , wherein said one or more amorphous phosphate salts is KH 2(1-x) PO (4-x) , wherein x is 1; and wherein said one or more oxysalts is BaSO 4 .

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Classifications

  • with alkaline or alkaline earth metals · CPC title

  • characterised by dimensions, e.g. grain size (in a colloidal state B01J35/23; crystallite size B01J35/77) · CPC title

  • by splitting-off hydrogen or functional groups; by hydrogenolysis of functional groups {(C07C51/36 - C07C51/373 take precedence)} · CPC title

  • with metals {other than Al or Zr} · CPC title

  • with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium · CPC title

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What does patent US11090639B2 cover?
Hydroxypropionic acid, hydroxypropionic acid derivatives, or mixtures thereof are dehydrated using a catalyst and a method to produce bio-acrylic acid, acrylic acid derivatives, or mixtures thereof. A method to produce the dehydration catalyst is also provided.
Who is the assignee on this patent?
Procter & Gamble
What technology area does this patent fall under?
Primary CPC classification B01J27/1806. Mapped technology areas include Operations & Transport.
When was this patent published?
Publication date Tue Aug 17 2021 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 12 related publications on this page (citations in our corpus or others sharing the same primary CPC).