Rate/kinetic selective multiple bed adsorption process cycle
US-11883775-B2 · Jan 30, 2024 · US
US9725378B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9725378-B2 |
| Application number | US-201514624861-A |
| Country | US |
| Kind code | B2 |
| Filing date | Feb 18, 2015 |
| Priority date | Mar 20, 2014 |
| Publication date | Aug 8, 2017 |
| Grant date | Aug 8, 2017 |
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The invention relates to a p-xylene separation process wherein at least a portion of ethylbenzene present in an aromatics-containing feed is removed prior to isomerization. Aspects of the invention provide a process for producing p-xylene. The process includes providing a first mixture comprising ≧5.0 wt. % of aromatic C 8 isomers, the C 8 isomers comprising p-xylene and ethylbenzene. A p-xylene-containing portion and an ethylbenzene-containing portion are separated from the first mixture in a first separation stage to form a p-xylene-depleted raffinate. The first separation stage can include at least one simulated moving-bed adsorptive separation stage. At least a portion the p-xylene-depleted raffinate in the liquid phase is reacted to produce a reactor effluent comprising aromatic C 8 isomers. The first mixture can be combined with ≧50.0 wt. % of the reactor effluent's aromatic C 8 isomers. The combining can be carried out before and/or during the separating of the p-xylene and ethylbenzene portions.
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What is claimed is: 1. A process for producing p-xylene, the process comprising: (a) providing a first mixture comprising aromatic C 8 isomers; (b) separating from the first mixture in a first stage: (i) a p-xylene-depleted raffinate; (ii) a p-xylene-containing portion comprising ≧10.0 wt. % of the mixture's p-xylene; and (iii) an ethylbenzene-containing portion comprising ≧10.0 wt. % of the mixture's ethylbenzene; wherein the first separation stage includes at least one simulated moving-bed adsorption chromatographic separation; (c) conducting away at least a portion of the separated p-xylene; (d) reacting at least a portion of the p-xylene-depleted raffinate in the liquid phase to produce a first reactor effluent comprising aromatic C 8 isomers; (e) separating from the first reactor effluent in a second separation stage a toluene-containing fraction and a xylene-enriched raffinate; (f) separating from the xylene-enriched raffinate an o-xylene-containing distillate; (g) recycling at least a portion of the o-xylene-containing distillate directly to the reacting in (d); (h) conducting away ≧50.0 wt. % of the ethylbenzene separated in (b)(iii); and (i) exposing ≦10.0 wt. % of aromatic C 8 isomers in the process to vapor-phase isomerization to produce a second reactor effluent comprising aromatic C 8 isomers. 2. The process of claim 1 , wherein the first mixture comprises ≧50.0 wt. % of a mixture of p-xylene, ethylbenzene, m-xylene, and o-xylene. 3. The process of claim 1 , wherein the first mixture comprises about 17 wt. % to 27 wt. % p-xylene, 40 wt. % to 50 wt. % m-xylene, 18 wt. % to 28 wt. % o-xylene, and 5 wt. % to 15 wt. % ethylbenzene. 4. The process of claim 1 , wherein reacting at least a portion the p-xylene-depleted raffinate in the liquid phase includes one or more transalkylation reactions. 5. The process of claim 1 , further comprising: (j) separating from the first reactor effluent in the second separation stage at least a portion of any C 1 -C 7 compounds produced during the reacting in (d); and (k) conducting the separated C 1 -C 7 compounds away from the process. 6. The process of claim 1 , further comprising separating from the first mixture in the first separation stage ≧50.0 wt. % of any non-aromatic hydrocarbon molecules. 7. The process of claim 1 , wherein the reacting in (d) includes liquid-phase isomerization, and wherein ≦10.0 wt. % of the p-xylene-depleted raffinate is in the vapor phase during the reacting. 8. The process of claim 1 , wherein ≦1.0 wt. % of the p-xylene-depleted raffinate is in the vapor phase during the reacting. 9. The process of claim 1 , wherein (i) ≧90.0 wt. % of the first mixture's ethylbenzene is separated by chromatographic separation in the first separation stage, (ii) ≧90.0 wt. % of the separated ethylbenzene is conducted away from the process, and (iii) ≧90.0 wt. % of the reactor effluent's aromatic C 8 isomers are combined with the first mixture in step (d). 10. The process of claim 1 , wherein the p-xylene-containing portion further comprises a desorbent from the separating in (b); wherein the process further comprises: (l) separating from the p-xylene containing portion a distillate fraction comprising the desorbent; and (m) recycling the distillate fraction to the separating in (b). 11. The process of claim 10 , further comprising: (n) separating from the p-xylene-containing portion a residue comprising p-xylene during the separating in (l); and (o) concentrating a p-xylene content of the residue in a crystallization zone to produce a concentrated p-xylene stream and a liquid stream; (p) recycling the liquid stream to the separating in (b).
by adsorption, i.e. purification or separation of hydrocarbons with the aid of solids, e.g. with ion-exchangers · CPC title
Catalytic processes · CPC title
by cracking a single hydrocarbon or a mixture of individually defined hydrocarbons or a normally gaseous hydrocarbon fraction · CPC title
Xylenes · CPC title
of the pentasil type, e.g. types ZSM-5, ZSM-8 or ZSM-11 · CPC title
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