Purification of recycled and renewable organic material

Patent metadata

Field	Value
Publication number	US-11499104-B2
Application number	US-201917261679-A
Country	US
Kind code	B2
Filing date	Jul 19, 2019
Priority date	Jul 20, 2018
Publication date	Nov 15, 2022
Grant date	Nov 15, 2022

Abstract

A method is disclosed of purifying a recycled or renewable organic material, wherein the recycled or renewable organic material includes more than 1 ppm silicon as silicon compounds and/or more than 10 ppm phosphorous as phosphorous compounds. The method can include providing a feed of the lipid material; heat treating the organic material in presence of an adsorbent and the filtering organic material and hydrotreating the lipid material in a presence of a hydrotreating catalyst to obtain purified hydrotreated organic material having less than 20% organic material and/or less than 30% of the original phosphorous content of the organic material.

First claim

The invention claimed is:

1. A method of purifying a recycled or renewable organic material, having more than 1 ppm silicon as silicon compounds and/or more than 10 ppm phosphorous as phosphorous compounds, the method comprising:
(a) providing a feed of the recycled or renewable organic material, wherein the recycled or renewable organic material is selected from a group consisting of plant based fats and oils, animal based fats and oils, fossil waste-based oils, waste oils, algal oils and microbial oils;
(b) optionally pre heat treating the recycled or renewable organic material at 180 to 325° C. and optionally adding acid before or after the heat treatment process and optionally filtering the pre heat treated recycled or renewable organic material;
(c) heat treating the recycled or renewable organic material in a presence of an adsorbent selected from silica-based adsorbents at 180 to 325° C. and filtering the heat treated recycled or renewable organic material, and optionally adding acid before or after the heat treatment process;
(d) optionally blending the heat treated recycled or renewable organic material with a hydrocarbon or lipid-based stream;
(e) optionally evaporating the volatile silicon compounds from the heat treated recycled or renewable organic material; and
(f) hydrotreating the heat treated recycled or renewable organic material in a presence of a hydrotreating catalyst;
to obtain purified hydrotreated recycled or renewable organic material selected to contain at least one or more of less than 20%, or less than 10%, or less than 5%, of the original silicon content of the recycled or renewable organic material provided in step (a) and/or less than 30% of the original phosphorous content of the recycled or renewable organic material provided in step (a).

2. A method as claimed in claim 1 , wherein the recycled or renewable organic material comprising:
(b) preheat treating at 180 to 325° C. to form a heat treated recycled or renewable organic material.

3. A method as claimed in claim 2 , comprising:
performing heat treatment in step (b) at a temperature range selected to be one or more of from 200 to 300° C., or from 240 to 280° C.

4. A method as claimed in claim 3 , wherein the residence time is selected to be within one or more ranges of from 1 to 300 min, or from 5 to 90 min, or from 20 to 40 min in heat treatment of step (b).

5. A method as claimed in claim 4 , wherein evaporation in step (e) is selected to be within one or more ranges of at 150° C. to 225° C., or at 160° C. to 200° C., or at 160 to 180° C.

6. A method as claimed in claim 5 , wherein a pressure in evaporation of step (e) is selected to be within one or more ranges of from 0.1 to 5 kPa, or from 0.1 to 3 kPa.

7. A method as claimed in claim 6 , wherein in evaporation of step (e) 1 to 10 wt %, or from 1 to 8 wt %, or from 1 to 5 wt %, or from 1 to 3 wt %, of the heat treated recycled or renewable organic material is evaporated.

8. A method as claimed in claim 7 , wherein water is added to the heat treated recycled or renewable organic material so that the water content of the heat treated recycled or renewable organic material before evaporation step (e) selected to be within one or more ranges of from 1 to 5 wt %, or from 1.5 to 4 wt %, or from 2 to 3 wt %.

9. A method as claimed in claim 8 , wherein the temperature in step (c) is selected to be within one or more ranges of from 200 to 300° C., or from 240 to 280° C.

10. A method as claimed in claim 9 , wherein a residence time is selected to be within one or more ranges of from 1 to 300 min, or from 5 to 240 min, or from 30 to 90 min in step (c).

11. A method as claimed in claim 10 , wherein a pressure in step (c) is from 500 to 5000 kPa, or from 800 to 2000 kPa.

12. A method as claimed in claim 11 , wherein the silica-based adsorbent is selected from a group consisting of alumina silicate, silica gel and mixtures thereof.

13. A method as claimed in claim 12 , wherein an amount of adsorbent is from 0.1 to 10.0 wt-%, or 0.5 to 2.0 wt %, of a total weight of the treated recycled or renewable organic material.

14. A method as claimed in claim 13 , wherein acid is added before or after heat treatment in step (c).

15. A method as claimed in claim 14 , wherein hydrotreating step (f) takes place under continuous hydrogen flow.

16. A method as claimed in claim 15 , wherein in step (f) the continuous hydrogen flow has an H2/feed ratio selected to be within one or more ranges of from 500 to 2000 n-L/L, or from 800 to 1400 n-L/L.

17. A method as claimed in claim 16 , wherein step (f) is performed at a temperature selected to be within one or more ranges of from 270 to 380° C., or from 275-360° C., or from 300-350° C.

18. A method as claimed in claim 17 , wherein step (f) is performed under pressure from 4 to 20 MPa.

19. A method as claimed in claim 18 , wherein the hydrotreating catalyst in step (f) comprises at least one component selected from IUPAC group 6, 8 or 10 of the Periodic Table.

20. A method as claimed in claim 19 , wherein the hydrotreating catalyst in step (f) is a supported Pd, Pt, Ni, NiW, NiMo or a CoMo catalysts and the support is zeolite, zeolite-alumina, alumina and/or silica, NiW/Al 2 O 3 , NiMo/Al 2 O 3 or CoMo/Al 2 O 3 .

21. A method as claimed in claim 20 , wherein step (f) is accomplished by (f1) hydrodeoxygenating (HDO) the heat treated recycled or renewable organic material fraction.

22. A method as claimed in claim 21 , wherein step (f) is accomplished by (f1) hydrodeoxygenating (HDO) the heat treated recycled or renewable organic material fraction in a presence of a HDO catalyst at a temperature from 290 to 350° C. under pressure from 4 to 20 MPa and under continuous hydrogen flow to obtain purified recycled or renewable organic material selected to contain at least one or more of less than 20%, or less than 10%, or less than 5%, of the original silicon content of the recycled or renewable organic material provided in step (a).

23. A method as claimed in claim 22 , wherein in step (f1) the HDO catalyst is sulfided NiW, NiMO or CoMo catalyst.

24. A method as claimed in claim 23 , wherein in step (f1) the continuous hydrogen flow has an H2/feed ratio from 500 to 2000 n-L/L, or from 800 to 1400 n-L/L.

25. A method as claimed in claim 24 , wherein a part of the hydrotreated product is recycled in step (f).

26. A method as claimed in claim 25 , wherein a ratio of the fresh feed to the hydrotreated product is from 2:1 to 20:1.

27. A method as claimed in claim 26 , wherein in step (d) the hydrocarbon or lipid-based stream is vacuum gas oil (VGO) or animal fat.

28. A process for producing recycled or renewable hydrocarbons, comprising:
(x) purifying the recycled or renewable organic material as claimed in claim 1 ; and
(y) subjecting the purified recycled or renewable organic material to an oil refinery conversion process, wherein the oil refinery conversion process includes altering a molecular weight of the feed, removal of heteroatoms from the feed, altering a degree of saturation of the feed, rearranging the molecular structure of the feed, or any combination thereof to obtain at least one recycled or renewable hydrocarbon.

29. A process as claimed in claim 28 , wherein step (y) is hydrocracking.

30. A process as claimed in claim 28 , wherein step (y) is perform

Assignees

• Neste Oyj

Inventors

• Toukoniitty Blanka
• Paasikallio Ville
• Pasanen Jukka-Pekka
• Touronen Jouni
• Hovi Meri
• Pasanen Antti
• Likander Salla
• Toppinen Sami
• Aalto Pekka
• Jansson Kari
• Lindblad Marina
• Käldström Mats
• Lamminpää Kaisa

Classifications

• C11B3/006

  by extraction · CPC title

• C10G69/06 Primary

  including at least one step of thermal cracking in the absence of hydrogen · CPC title

• C11B3/04

  with acids · CPC title

• C11B3/10 Primary

  by adsorption · CPC title

• C10G2300/1011

  Biomass · CPC title