Heavy petroleum residue derived iron incorporated sp2 carbon nanogranules for improved synthesis of light olefins

Patent metadata

Field	Value
Publication number	US-10526257-B2
Application number	US-201916441943-A
Country	US
Kind code	B2
Filing date	Jun 14, 2019
Priority date	Nov 2, 2016
Publication date	Jan 7, 2020
Grant date	Jan 7, 2020

Abstract

Present invention relates to sp 2 carbon nanogranules with iron incorporated in it from heavy petroleum residue of a refinery and thereby utilizing the materials for improved synthesis of light olefins (C 2 -C 4 ) from syngas in a single step Fischer Tropsch synthesis to lower olefins, (FTO). The efficient iron incorporated carbon nanogranules derived from low value heavy petroleum residue are very attractive as catalytic system for direct synthesis of light olefin (C 2 -C 4 ) from syngas at CO conversion up to 30%.

First claim

We claim:

1. A process for the direct synthesis of lower olefins from syngas using an iron incorporated sp 2 carbon nanogranules (Fe/CNG) catalyst, the catalyst comprising (a) iron in the form of Fe(0), in bulk phase, (b) iron in the form of Fe(0) along with the Fe 3 C phase, and (c) trace amounts of Fe(II) and Fe(III), where (a), (b) and (c) are collectively present in the range from 5 to 20 w/w % of the sp2 carbon nanogranules, and wherein the trace amounts of Fe(ii) and Fe(III) are found on a surface of the sp2 carbon nanogranules, the process comprising the steps of:
i. reducing the Fe/CNG catalyst under hydrogen or diluted hydrogen under pressure of atmospheric to 10 bar_g at a temperature in the range of 350 to 500° C. for a period in the range of 2 to 12 hours;
ii. cooling the catalyst followed by heating under the flow of syngas and nitrogen with H 2 to CO mole ratio is in the range of 0.5:1 to 2:1 at GHSV of 2000 to 5000 mLh −1 g −1 at a temperature in the range of 300 to 380° C. under atmospheric pressure; and
iii. pressurizing the bed at 5 to 30 bar to obtain lower olefins.

2. The process of claim 1 , further comprising, prior to step (i):
iv. dissolving heavy petroleum residue or vacuum residue in a solvent along with iron precursor to prepare a homogeneous solution;
v. pumping the homogeneous solution as obtained in step (iv) at flow range of 0.5 mL/min to 5 mL/min to a quartz reactor tube placed in a furnace and spraying the solution to a reactor tube in presence of nitrogen flow in the range of 100 to 300 mL/min for a time period of 10 minute to 60 minutes to obtain carbon deposited on tube surface;
vi. cooling the tube and collecting the carbon deposits from the surface as obtained in step (v.) of the reactor tube followed by washing with solvent to remove any unconverted residue; and
vii. drying the carbon deposits as obtained in step (vi) and calcining at temperature in the range of 400 to 700° C. for a period in the range of 1 to 6 hours under nitrogen flow at 50 to 150 mL/min to obtain iron incorporated carbon nanogranules (Fe/CNG).

3. The process as claimed in claim 2 , wherein the heavy petroleum residues used is vacuum residue from refinery consisting of polyaromatic hydrocarbons (PAH).

4. The process as claimed in claim 2 , wherein the solvent used in step (iv or v) is an aromatic solvent selected from the group consisting of light naphtha, petroleum ether, benzene, toluene, xylene and ethylbenzene.

5. The process as claimed in claim 2 , wherein the iron precursor used is an organometallic compound of iron.

6. The process as claimed in claim 2 , wherein the iron precursor used is ferrocene.

7. The process as claimed in claim 2 , wherein the weight composition of the heavy petroleum residue or vacuum residue used is in the range of 5 to 20%.

8. The process as claimed in claim 2 , wherein weight composition of the iron precursor used is in the range of 5 to 20%.

9. The process as claimed in claim 1 , wherein CO conversion efficiency is up to 30% and selectivity of light olefins is up to 50%.

10. The process as claimed in claim 1 , wherein the light olefins from syngas obtained at lower rate of methanation of 15 to 17% and reduced conversion of CO to CO 2 at 12 to 15% with respect to the hydrocarbons.

Assignees

• Council Scient Ind Res

Inventors

• Ghosh Indrajit Kumar
• Umesh Kumar
• Bordoloi Ankur

Classifications

• B01J21/18

  Carbon · CPC title

• B01J37/04

  Mixing {(B01J37/0009, B01J37/0018 take precedence)} · CPC title

• C07C1/0445

  Preparation; Activation · CPC title

• B01J37/06

  Washing {(B01J37/0009, B01J37/0018 take precedence)} · CPC title

• B01J37/086

  Decomposition of an organometallic compound, a metal complex or a metal salt of a carboxylic acid · CPC title