A method for degrading a plastic

Patent metadata

Field	Value
Publication number	US-2016280881-A1
Application number	US-201415034655-A
Country	US
Kind code	A1
Filing date	Nov 4, 2014
Priority date	Nov 5, 2013
Publication date	Sep 29, 2016
Grant date	—

Abstract

The present invention relates to a method for degrading a plastic containing non-biodegradable polymers comprising submitting said plastic to at least one enzyme for modifying a polymer of said plastic which has a methane potential less than 5 Nm3/t+/−20%, wherein at least one product resulting from the modification exhibits a methane potential greater than 10 Nm3/t+/−20%.

First claim

1 - 17 . (canceled)

18 . A method for treating a plastic comprising exposing said plastic to at least one enzyme for modifying a polymer of said plastic which has a methane potential less than 5 Nm3/t+/−20%, wherein at least one product resulting from the modification exhibits a methane potential greater than 10 Nm3/t+/−20%.

19 . The method according to claim 18 , wherein the enzyme is a hydrolase selected from the group consisting of a cutinase, lipase, esterase, carboxylesterase, p-nitrobenzylesterase, protease, serine protease, amidase, aryl-acylamidase, urethanase, oligomer hydrolase or an oxidative enzyme selected from the group consisting of a laccase, lipoxygenase, peroxidase, haloperoxidase, mono-oxygenase, di-oxygenase and hydroxilase.

20 . The method according to claim 18 , wherein the resulting product exhibits a methane potential comprised between 10 and 1000 Nm3/t.

21 . The method according to claim 18 , wherein the resulting product exhibits a methane potential at least 10 times higher than the methane potential of the original polymer.

22 . The method according to claim 18 , wherein the original polymer is selected from the group consisting of polyolefins, ethylene vinyl alcohol (EVOH), poly lactic acid (PLA), polyethylene terephthalate (PET), polybutylene terephthalate (PBT), polytrimethylene terephthalate (PTT), polyethylene isosorbide terephthalate (PEIT), polyethylene furanoate (PEF), polyamide (PA), polyamide-6 or Poly(ε-caprolactam) or polycaproamide (PA6), polyamide-6,6 or Poly(hexamethylene adipamide) (PA6,6), Poly(l1-aminoundecanoamide) (PA11). polydodecanolactam (PA12), poly(tetramethylene adipamide) (PA4,6), poly(pentamethylene sebacamide) (PA5,10), polyhexamethylene nonanediamideaamide (PA6,9), poly(hexamethylene sebacamide) (PA6,10), poly(hexamethylene dodecanoamide) (PA6,12), poly(m-xylylene adipamide) (PAMXD6), polyhexamethylene adipamide/polyhexamethyleneterephtalamide copolymer (PA66/6T), polyhexamethylene adipamide/polyhexamethyleneisophtalamide copolymer (PA66/6I) polyurethane (PL), polyvinyl chloride (PVC), polystyrene (PS), acrylonitrile butadiene styrene (ABS), poly(oxide phenylene) (PPO), polycarbonate (PC), copolymer of phosphono and carboxylic acid (PCA), polyacrylate, polymethacrylate methyle (PMMA), polyoxymethylene (POM), styrene acrylonitrile (SAN), polyester polymer alloy (PEPA), polyethylene naphthalate (PEN), styrene-butadiene (SB), and blends/mixtures of these materials.

23 . The method according to claim 18 , wherein the original polymer is a polyolefin polymer.

24 . The method according to claim 23 , wherein the polyolefin polymer is selected from the group consisting of polyethylene, polypropylene, polymethylpentene, polybutene-1, polyisobutylene, ethylene propylene rubber and ethylene propylene diene monomer rubber.

25 . The method according to claim 18 , wherein the original polymer is a polyester polymer.

26 . The method according to claim 25 , wherein the polyester polymer is selected from the group consisting of poly lactic acid (PLA), polyethylene terephthalate (PET), polybutylene terephthalate (PBT), polytrimethylene terephthalate (PTT), polyethylene isosorbide terephthalate (PEIT) and polyethylene furanoate (PEF).

27 . The method according to claim 18 , wherein the original polymer is a polyamide polymer.

28 . The method according to claim 27 , wherein the polyamide polymer is selected from the group consisting of polyamide-6 or Poly(ε-caprolactam) or polycaproamide (PA6), polyamide-6,6 or Poly(hexamethylene adipamide) (PA6,6) and Poly(11-aminoundecanoamide) (PA11).

29 . The method according to claim 18 , wherein the plastic further comprises at least one polymer selected from the group consisting of aliphatic polyester, polyvinyl alcohol, cellulose, polylactic acid (PLA), polyhydroxyalkanoate (PHA), starch-based polymers, poly(butylene adipate-co-terephthalate) (PBAT), polybutylene succinate (PBS), polybutylene succinate adipate (PBSA), and polycaprolactone (PCL).

30 . The method according to claim 18 , comprising a preliminary step for mechanically and/or physically and/or chemically degrading said plastic.

31 . The method according to claim 18 , wherein the enzyme is used together with at least one mediator compound or cofactor mediating the enzymatic modification of the original polymer.

32 . The method according to claim 18 , comprising contacting the plastic with at least one microorganism expressing at least one enzyme modifying the original polymer, or extract thereof.

33 . The method according to claim 32 , wherein the microorganism further produces at least one mediator compound mediating the enzymatic modification of the original polymer.

34 . The method according to claim 32 , wherein the microorganism is selected from the group consisting of Amycolatopsis, Tritirachium, Kibdelosporangium, Actinomadura, Bionectria, Thermomonospora, Isaria, Bacillus, Acinetobacter, Arthrobacter, Pseudomonas, Sphingomonas, Saccharomyces, Aspergillus, Fusarium, Beauveria, Brevibacillus, Candida, Chaetomium, Cladosporium, Comamonas, Coriolus, Coryneformes, Corynebacterium, Cunninghamella, Delftia, Dictyoglomus, Diplococcus, Engyodontium, Enterobacter, Flavobacterium, Gliocladium, Hansenula, Kluyveromyces, Leptothrix, Listeria, Microbacterium, Micrococcus, Moraxella, Mortierella, Mucor, Mycobacterium, Nocardia, Paecylomyces, Paenibacillus, Penicillium, Phanerochaete, Pleurotus, Proteobacterium, Proteus, Pullularia, Rahnella, Ralstonia, Rhodococcus, Saccharomyces, Serratia, Sphingomonas, Streptomyces, Staphylococcus, Stenotrophomonas, Streptococcus, Talaromyces, Trametes, Trichoderma , and Vibrio.

35 . The method according to claim 18 , further comprising subjecting the product exhibiting a methane potential to a methane fermentation step.

36 . The method according to claim 33 , wherein the modification step and the methane fermentation step are performed sequentially or simultaneously.

37 . A method for improving the methane potential of a non-biodegradable polymer plastic comprising exposing said plastic to an enzyme or microorganism that cleaves carbon-carbon or esters bonds, wherein the resulting product exhibits a methane potential at least 10 times higher.

Assignees

• Carbios

Inventors

• Boisart Cédric
• Maille Emmanuel
• Guillamot Frédérique

Classifications

• B09B3/65

  Anaerobic treatment · CPC title

• B09B3/35

  Shredding, crushing or cutting · CPC title

• B09B3/60

  Biochemical treatment, e.g. by using enzymes · CPC title

• B09B3/70

  Chemical treatment, e.g. pH adjustment or oxidation (involving an extraction step B09B3/80) · CPC title

• C08J11/105 Primary

  by treatment with enzymes · CPC title