IP Library Granted Patent US 7,348,466
Granted Patent B2
US 7,348,466 · App. 11/104,990 · Granted Mar 25, 2008

Solvent extraction

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Quick Facts
Patent No.
US 7,348,466
App. No.
11/104,990
Granted
Mar 25, 2008
Kind
B2
Abstract

In a method for the solvent extraction of butadiene from a mixture of hydrocarbons having four carbon atoms per molecule, which method inherently produces tars, the extraction process is operated with a tar loading level, relative to the solvent employed, of no more than about 1.6 wt. %.

Claims (11)

1. In a process for the solvent extraction of butadiene from a mixture of C 4 compounds that boil close to butadiene and the recovery of butadiene as a product of the process, wherein at least one solvent extraction step is employed using at least one lean solvent that preferentially extracts butadiene from said mixture of C 4 'S to form a solvent extract stream that carries butadiene and tars that form during said butadiene extraction process, said extract being subjected to a stripping operation to separate butadiene from said solvent and tars, the butadiene separated from said solvent and tars being recovered as a product of the process, a separate primary mixture of solvent and tars being recovered for reuse in said at least one solvent extraction step, and wherein a secondary portion of said primary mixture of solvent and tars is separated from said primary mixture and subjected to a reclamation step in which substantial quantities of tars are removed from said secondary portion and from said extraction process thereby forming a secondary lean solvent stream that is essentially depleted in its content of tars, and reintroducing said secondary lean solvent stream into said extraction process to absorb additional butadiene, the improvement comprising operating said extraction process in a manner such that sufficient tars are removed from said extraction process to maintain the amount of tars present in said extraction process at a level no greater than about 1.6 wt. %, based on the total weight of solvent and tars in said extraction process.

2. The method of claim 1 wherein two solvents are employed in said extraction process, the first of said solvents being employed in a major amount and the second of said solvents being employed in a minor amount, said extraction process including said reclamation step is operated in a manner to maintain the total amount of secondary solvent and tars in said extraction process at a level of less than 5 wt. % based on the total weight of both solvents and tars in said extraction process.

3. The method of claim 1 wherein said reclamation step employs at least one reboiler with an overhead vapor condenser system in which solvent is boiled as vapor overhead from said tars and condensed to an essentially tar free liquid for reintroduction into said extraction process and tars are left in said reboiler for separate removal from said extraction process, said tars in said reboiler having an upper level in said reboiler above which is vapor space, said reboiler being operated in a manner such that said tar laden secondary portion solvent feed to said reboiler is at least one of 1) introduced into said reboiler below said tar level at a temperature sufficient to prevent foaming in said reboiler, and 2) introduced into said reboiler vapor space above said tar level.

4. The method of claim 3 wherein said tar laden solvent introduced below said tar level is sufficiently cool to essentially avoid flashing of said solvent while below said tar level.

5. The method of claim 3 wherein said tar laden solvent introduced above said tar level is heated to a temperature that can cause at least some flashing of said solvent while it is in said vapor space above said tar level.

6. The method of claim 2 wherein two solvent extractors are employed each associated with stripper units for separating tar laden solvent for reuse in said extraction process including said reclamation step, the primary mixture of solvent and tars from each of said associated strippers being combined to form a single primary mixture of solvent and tars, and a secondary portion of said single primary mixture is split off there from for tar separation in said reclamation step.

7. The method of claim 6 wherein said reclamation step employs at least one kettle reboiler with an overhead condenser system in which solvent is boiled as vapor overhead from said tars and condensed to liquid for reintroduction into said extraction process and tars are left in said reboiler for separate removal from said extraction process, said tars in said reboiler having an upper level above which is vapor space, said reboiler being operated in a manner such that tar laden secondary portion solvent feed to said reboiler is at least one of 1) introduced into said reboiler below said tar level at a temperature sufficient to prevent solvent/tar foaming in said reboiler and consequent carryover of tars into said overhead, and 2) introduced into said reboiler in said vapor space above said tar level.

8. The method of claim 2 wherein said solvents are dimethylformamide and furfural, said dimethylformamide being present in an amount greater than about 90 wt. %, and said furfural being present in an amount less than about 10 wt. %, both wt. % being based on the combined total weight of both solvents and tars, and essentially all tars are removed from said secondary portion of said primary mixture of solvents and tars before said reclaimed solvent is reintroduced into said extraction process.

9. The method of claim 8 wherein said secondary portion of said primary mixture of solvent and tars is from about 0.1 wt. % to about 1.6 wt. % of said primary mixture based on the total weight of said primary mixture.

10. The method of claim 9 wherein said extraction process including said reclamation step is operated so as to maintain in said extraction process both 1) the amount of tars at a level of less than 1.6 wt. %, and 2) the total amount of tars and secondary solvent at a level of less than 5 wt. %, all wt. % being based on the total weight of solvents and tars in said extraction process.

11. The method of claim 1 wherein said tars are polymers formed from said C 4 compounds, said polymers being not readily vaporizable under the operating conditions of temperature and pressure of said extraction process.

Assignments (18)
RELEASE OF SECURITY INTEREST Recorded Jan 22, 2014
From: WELLS FARGO BANK, NATIONAL ASSOCIATION
To: EQUISTAR CHEMICALS, LP
Reel/Frame 032112/0786 →
APPOINTMENT OF SUCCESSOR ADMINISTRATIVE AGENT Recorded Jan 22, 2014
From: UBS AG, STAMFORD BRANCH
To: BANK OF AMERICA, N.A.
Reel/Frame 032112/0863 →
RELEASE OF SECURITY INTEREST Recorded Jan 22, 2014
From: CITIBANK, N.A.
To: EQUISTAR CHEMICALS, LP
Reel/Frame 032113/0644 →
RELEASE OF SECURITY INTEREST Recorded Jan 22, 2014
From: DEUTSCHE BANK TRUST COMPANY AMERICAS
To: EQUISTAR CHEMICALS, LP
Reel/Frame 032113/0684 →
RELEASE OF SECURITY INTEREST Recorded Jan 22, 2014
From: BANK OF AMERICA, N.A.
To: EQUISTAR CHEMICALS, LP
Reel/Frame 032113/0730 →
SECURITY AGREEMENT Recorded May 19, 2010
From: EQUISTAR CHEMICALS, LP
To: WELLS FARGO BANK, NATIONAL ASSOCIATION, AS COLLATERAL AGENT
Reel/Frame 024402/0655 →
SECURITY AGREEMENT Recorded May 18, 2010
From: EQUISTAR CHEMICALS, LP
To: CITIBANK, N.A., AS ADMINISTRATIVE AGENT
Reel/Frame 024397/0861 →
SECURITY AGREEMENT Recorded May 7, 2010
From: EQUISTAR CHEMICALS. LP
To: UBS AG, STAMFORD BRANCH, AS COLLATERAL AGENT
Reel/Frame 024351/0001 →
SECURITY AGREEMENT Recorded May 6, 2010
From: EQUISTAR CHEMICALS, LP
To: DEUTSCHE BANK TRUST COMPANY AMERICAS, AS COLLATERAL AGENT
Reel/Frame 024342/0443 →
RELEASE OF SECURITY INTEREST Recorded May 5, 2010
From: CITIBANK, N.A., AS COLLATERAL AGENT
To: LYONDELL CHEMICAL TECHNOLOGY, L.P.; EQUISTAR CHEMICALS, LP
Reel/Frame 024337/0705 →
RELEASE OF SECURITY INTEREST Recorded May 5, 2010
From: UBS AG, STAMFORD BRANCH, AS COLLATERAL AGENT
To: EQUISTAR CHEMICALS, LP
Reel/Frame 024337/0186 →
RELEASE OF SECURITY INTEREST Recorded May 5, 2010
From: CITIBANK, N.A., AS COLLATERAL AGENT
To: LYONDELL CHEMICAL TECHNOLOGY, L.P.; EQUISTAR CHEMICALS, LP
Reel/Frame 024337/0856 →
RELEASE OF SECURITY INTEREST Recorded May 4, 2010
From: CITIBANK, N.A., AS COLLATERAL AGENT
To: EQUISTAR CHEMICALS, LP
Reel/Frame 024329/0535 →
SECURITY AGREEMENT Recorded Oct 30, 2009
From: EQUISTAR CHEMICALS, LP
To: UBS AG, STAMFORD BRANCH, AS COLLATERAL AGENT
Reel/Frame 023449/0687 →
SECURITY AGREEMENT Recorded Apr 9, 2009
From: EQUISTAR CHEMICALS, LP
To: CITIBANK, N.A., AS ADMINISTRATIVE AGENT AND COLLATERAL AGENT
Reel/Frame 022678/0860 →
SECURITY AGREEMENT Recorded Aug 4, 2008
From: BASELL POLYOLEFINE GMBH; ARCO CHEMICAL TECHNOLOGY L.P.; ARCO CHEMICAL TECHNOLOGY, INC.; ATLANTIC RICHFIELD COMPANY; BASELL NORTH AMERICA, INC.; BASELL POLYOLEFIN GMBH; LYONDELL CHEMICAL COMPANY; EQUISTAR CHEMICALS, L.P.
To: CITIBANK, N.A., AS COLLATERAL AGENT
Reel/Frame 021354/0708 →
GRANT OF SECURITY INTEREST IN UNITED STATES PATENTS AND PATENT APPLICATIONS Recorded Mar 26, 2008
From: BASELL POLYOLEFINE GMBH; ARCO CHEMICAL TECHNOLOGY L.P.; ARCO CHEMICAL TECHNOLOGY, INC.; ATLANTIC RICHFIELD COMPANY; BASELL NORTH AMERICA, INC.; EQUISTAR CHEMICALS. LP.; LYONDELL CHEMICAL COMPANY; LYONDELL CHEMICAL TECHNOLOGY, L.P.; LYONDELL PETROCHEMICAL COMPANY; NATIONAL DISTILLERS AND CHEMICAL CORPORATION; OCCIDENTAL CHEMICAL CORPORATION; OLIN CORPORATION; QUANTUM CHEMICAL CORPORATION; BASELL POLYOLEFIN GMBH
To: CITIBANK, N.A., AS COLLATERAL AGENT
Reel/Frame 020704/0562 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 13, 2005
From: BRIDGES, JOSEPH P.; WILLIAMS, SOLON B.; UNTERBRINK, BYRON B.
To: EQUISTAR CHEMICALS, LP
Reel/Frame 016471/0551 →