Process for treating a gaseous effluent from pyrolytic decomposition of a polymer

1. A process for treating a gaseous effluent obtained from a pyrolytic decomposition of a polymer or of a polymer blend, for recovering one or more monomers contained in said gaseous effluent, said process comprising the following steps:

a condensation step which consists in injecting the gaseous effluent into a condensation chamber maintained at a first pressure p 1 , and in placing the gaseous effluent in contact with an absorbent liquid, the temperature of said absorbent liquid being below the temperature of the gaseous effluent, so that said monomer(s) condense(s) in the absorbent liquid by heat exchange,

a step of partial vaporization of a condensate obtained on conclusion of the condensation step, by expansion of the condensate in a second chamber maintained at a second pressure p 2 below the first pressure p 1 ,

a reinjection step which consists in at least partly redirecting a first liquid or vapor fraction, obtained on conclusion of the partial vaporization step, to the condensation chamber to once again absorb the monomer(s) contained in the gaseous effluent, and

a recovery step including purification of a second liquid or vapor fraction, obtained on conclusion of the partial vaporization step and charged with the monomer(s).

2. The process as claimed in claim 1 , wherein the first pressure p 1 is between 0.1 and 5 bar.

3. The process as claimed in claim 1 , wherein the temperature of the absorbent liquid is at least 50° C. below the temperature of the gaseous effluent.

4. The process as claimed in claim 1 , wherein the temperature of the absorbent liquid is not more than 450° C. below the temperature of the gaseous effluent.

5. The process as claimed in claim 1 , wherein the temperature of the absorbent liquid is at least 50° C. and not more than 450° C. below the temperature of the gaseous effluent.

6. The process as claimed in claim 1 , wherein the second chamber is maintained at a pressure p 2 of between 0.001 and 0.8 bar.

7. The process as claimed in claim 1 , wherein the pressure difference as an absolute value between the condensation chamber and the second chamber is greater than or equal to 0.5 bar.

8. The process as claimed in claim 1 , wherein the recovery step includes condensation of the vapor fraction obtained on conclusion of the partial vaporization step if the second fraction charged with the monomer(s) is a vapor fraction.

9. The process as claimed in claim 1 , wherein the recovery step includes filtration or decantation of the liquid fraction obtained on conclusion of the partial vaporization step if the second fraction charged with the monomer(s) is a liquid fraction.

10. The process as claimed in claim 1 , wherein during the reinjection step, the first fraction reinjected is a liquid fraction and during the recovery step, the second fraction recovered is a vapor fraction.

11. The process as claimed in claim 1 , wherein the absorbent liquid is selected so that the ratio between the absorbent liquid's latent heat of vaporization ΔHv in the standard state and the absorbent liquid's molar specific heat Cp in the standard state is greater than that of the monomer(s) to be recovered.

12. The process as claimed in claim 1 , wherein the absorbent liquid is chosen from one of the following compounds: benzene, benzonitrile, a compound of formula R—COOH, and a compound of formula R—OH, in which R is chosen from alkyls, the carbon number of which is between 1 and 5, a phenyl or a hydrogen.

13. The process as claimed in claim 1 , wherein the absorbent liquid is chosen from one of the following compounds: a compound of formula R—OH, a compound of formula R—COOH, in which R is chosen from alkyls, the carbon number of which is between 1 and 5, or a hydrogen.

14. The process as claimed in claim 1 , wherein the absorbent liquid is chosen from dihydrogen monoxide, methanol, ethanol, propanol, butanol, formic acid, acetic acid or mixtures thereof.

15. The process as claimed in claim 1 , wherein the absorbent liquid is chosen so that the absorbent liquid's boiling point is of the order of magnitude of that of the monomer(s) to be recovered ±80° C.

16. The process as claimed in claim 15 , wherein the absorbent liquid has a boiling point above or substantially equal to that of the monomer(s) to be recovered and/or of an azeotrope formed with the monomer(s) to be recovered.

17. The process as claimed in claim 1 , wherein the polymer is selected from: polyethylene; a homopolymer and copolymer of olefins; polypropylene, polybutadiene and polybutylene; acrylic homopolymers and copolymers and polyalkyl methacrylates; a polyhydroxyalkanoate; homopolyamides and copolyamides; polycarbonates; polyesters; polyethers; polystyrene; copolymers of styrene and maleic anhydride; poly (vinyl chloride); fluoropolymers; natural or synthetic rubbers; thermoplastic polyurethanes; polyaryl ether ketones (PAEK); polyetherimide; polysulfone; poly (phenylene sulfide); cellulose acetate; poly (vinyl acetate); polypropiolactone or a mixture of two or more of these polymers.

18. The process as claimed in claim 1 , wherein the monomer(s) are selected from the following compounds: methyl methacrylate, methyl acrylate, ethyl acrylate, acrylic acid, methacrylic acid, styrene, crotonic acid, gamma-butyrolactone, delta-valerolactone and mixtures thereof.

19. The process as claimed in claim 1 , wherein the injection of the gaseous effluent during the condensation step is performed co-currentwise or count-currentwise relative to the absorbent liquid.

20. The process as claimed in claim 1 , wherein the process also includes a separation step on the condensate obtained on conclusion of the condensation step before the partial vaporization step.

21. The process as claimed in claim 1 , wherein the process also includes a step of adjusting the temperature of the fraction redirected to the condensation chamber to once again absorb the monomer(s) contained in the gaseous effluent.

22. The process as claimed in claim 1 , wherein at the moment of the condensation step, additives are added to the absorbent liquid.

23. The process as claimed in claim 1 , wherein at the moment of the partial vaporization step ( 230 ), additives are added to the circuit.