Poly(acrylic acid) from bio-based acrylic acid and its derivatives
US-10344108-B2 · Jul 9, 2019 · US
US11090639B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11090639-B2 |
| Application number | US-202016871160-A |
| Country | US |
| Kind code | B2 |
| Filing date | May 11, 2020 |
| Priority date | Aug 28, 2015 |
| Publication date | Aug 17, 2021 |
| Grant date | Aug 17, 2021 |
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.
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.
Opening claim text (preview).
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 .
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
Related publications grouped by family.
Answers are generated from the same data shown on this page.