Process for propylene and LPG recovery in FCC fuel gas

Patent metadata

Field	Value
Publication number	US-10329223-B2
Application number	US-201615187005-A
Country	US
Kind code	B2
Filing date	Jun 20, 2016
Priority date	Jun 19, 2015
Publication date	Jun 25, 2019
Grant date	Jun 25, 2019

Abstract

The present invention provides a process for recovery of propylene and LPG from the fuel gas produced in FCC unit by contacting a heavier hydrocarbon feed with FCC catalyst. The process provides an energy efficient configuration for revamping an existing unit constrained on wet gas compressor capacity or for designing a new gas concentration unit to recover propylene and LPG recovery beyond 97 mole %. The process of the present invention provides an increase propylene and LPG recovery without loading wet gas compressor with marginal increase in liquid loads.

First claim

We claim:

1. A process for the recovery of propylene and LPG from a product mixture obtained by contacting a hydrocarbon feed with a catalyst in a FCC process, comprising the steps:
(i) distilling the product mixture in main fractionator to obtain heavier liquid product as side or bottom draws and a gaseous top product consisting of components boiling below 215° C.;
(ii) cooling and condensing the gaseous top product and separating obtained gas-liquid mixture in a receiver cum separator to obtain a liquid fraction referred to as unstabilized naphtha and a lighter gaseous fraction;
(iii) sequentially compressing, cooling and separating in a two stage wet gas compressor train said lighter gaseous fraction obtained from step (ii) to obtain gaseous fraction and liquid fraction from a high pressure separator;
(iv) mixing the liquid fraction as obtained from step (ii) with the liquid fraction as obtained from step (iii) in the high pressure separator to obtain combined liquid fraction;
(v) feeding the combined liquid fraction as obtained in step (iv) to a de-ethanizer to produce ethane and lighter components and a de-ethanized liquid product, wherein the ethane and lighter components are recycled back to the high pressure separator in step (iii) whereas the de-ethanized liquid product is fed to a debutanizer column;
(vi) separating butane and lighter components from the de-ethanized liquid product as overhead gaseous fraction and obtaining heavier fraction as bottom product referred to as debutanizer bottoms in the debutanizer column;
(vii) contacting the gaseous fraction obtained from the high pressure separator in step (iii) in an absorber with a part of the debutanizer bottoms as obtained in step (vi) to produce a rich oil and a gaseous fraction; and
(viii) feeding the rich oil from the absorber to the de-ethanizer via the high pressure separator,

wherein the process is characterized by feeding at least or a part of the unstabilized naphtha as obtained in step (ii) to the de-ethanizer via the high pressure separator and contacting a part of the debutanizer bottoms as obtained in step (vi) with the gaseous fraction obtained from the high pressure separator in step (iii) in the absorber, wherein the at least part of the unstabilized naphtha obtained in step (ii) is fed directly to the high pressure separator and then sequentially to the de-ethanizer, the debutanizer column and the absorber without butane and lighter components being first stripped off from the unstabilized naphtha in a separate column and recycled whereby to avoid a need for compression of the recycled lighter components.

2. The process as claimed in claim 1 , wherein an overhead condenser pressure in the main fractionator is from 10 prig and above.

3. The process as claimed in claim 1 , wherein the debutanizer bottoms are supplied to the absorber at temperature from about 20° C. to about 30° C., wherein the temperature is adjusted by using chilled water as an indirect cooling media.

4. The process as claimed in claim 1 , wherein the gaseous fraction from the absorber as obtained in step (vii) is further treated to recover gasoline range material.

5. The process as claimed in claim 2 , wherein the debutanizer bottoms are supplied to the absorber at temperature from about 20° C. to about 30° C., wherein the temperature is adjusted by using chilled water as an indirect cooling media.

6. The process as claimed in claim 2 , wherein the gaseous fraction from the absorber as obtained in step (vii) is further treated to recover gasoline range material.

7. The process as claimed in claim 3 , wherein the gaseous fraction from the absorber as obtained in step (vii) is further treated to recover gasoline range material.

8. The process as claimed in claim 1 , wherein an overhead condenser pressure in the main fractionator is from 25 psig and above.

9. The process as claimed in claim 1 , wherein all of the unstabilized naphtha as obtained in step (ii) is fed directly to the high pressure separator, without butane and lighter components being first stripped off from the unstabilized naphtha in a separate column and recycled, and is then de-ethanized and debutanized before being passed to the absorber.

10. The process as claimed in claim 1 , wherein the process consists essentially of the recited steps.

Assignees

• Reliance Industries Ltd

Inventors

• Yadav Manoj
• Das Asit Kumar
• Mandal Sukumar
• Parekh Amitkumar
• Limbasiya Nilamkumar

Classifications

• C10G70/048

  by liquid-liquid extraction · CPC title

• C10G2400/20

  C2-C4 olefins · CPC title

• C10G70/06

  by gas-liquid contact · CPC title

• C10L3/12

  Liquefied petroleum gas {(liquefying by pressure and cold treatment F25J)} · CPC title

• C07C7/04

  by distillation · CPC title