Recycling of polyesters

Abstract

The present invention is related to a process for the preparation of a purified solution (PS) containing a polyester depolymerization product, said method comprising the steps of forming a blend comprising a waste stream (W) of polyester and at least one diol monomer HO-R1-OH (A), which is capable of reacting with the polyester, exposing the blend to conditions suitable for at least partial depolymerization of the polyester, mixing the obtained depolymerization solution with a cooling liquid (C) and removing thus solidified liquifying contaminant in solid form, so as to obtain the purified solution (PS) containing the polyester depolymerization product, characterized in that the cooling liquid (C) is a portion of the purified solution (PS). The present invention is also related to a process for the preparation of a polyester from said purified solution (PS), and to a device for performing said processes.

Description

[0001] Recycling of polyesters

[0002] The present invention is related to a method for recycling of a polyester condensation polymer.

[0003] The preparation of polymers from their monomers is well known and established in large scale. Traditionally the used monomers are derived from fossil resources. The use of fossil resources is based on a linear product flow from fossil resource to polymer to waste. In the long term such linear product flows are not sustainable. As an alternative, the use of monomers derived from renewable resources is proposed to create a more cyclic product flow. However, the resulting cycle from polymer to CO2and water to plant based renewable resources to polymer is a long and energy intensive approach to provide polymers.

[0004] Especially condensation polymers have the advantage that they can be depolymerized into depolymerization products such as their monomers, dimers and / or oligomers and re-polymerized from such recycled depolymerization products.

[0005] Polyesters have a general structure comprising repeat units. They are typically prepared in large scale by polymerizing monomers with each other, wherein said monomers are diols and diacids. Alternatively, the polyesters can be prepared in large scale by polymerizing cyclic dimers or oligomers obtained from diol and diacid monomers. Due to ring opening polymerization, a polyester is formed.

[0006] These polyesters can be recycled by depolymerization with the addition of a diol monomer. The depolymerization results in a polyester depolymerization product, said polyester depolymerization product having a repeat unit [-A' ' -B' ' ] with the formula [-O-R1-OOC-R2-CO- ], and having 1 to 9 repeat units, wherein R1and R2are as defined below. For example, said polyester depolymerization product may be a recycled monomer product comprising a condensation monomer having the formula HO-R1-OOC-R2-COO-R1-OH or a dimer and / or oligomer thereof, wherein R1and R2are as defined below. The polyester depolymerization product, can be introduced into a conventional polyester preparation process starting from the diol and diacid monomers.

[0007] GB-610136 is an early description of a polyester being depolymerized with a glycol monomer and being re-polymerized from the depolymerization solution.

[0008] Various methods have been developed to clean the monomer product obtained by depolymerization. Reference is made to US-4, 609, 680, US-6, 642, 350, US-2006 / 074136 and US-6, 630, 601.

[0009] In WO 2023 / 217707 Al, a method for the preparation of a polyester from a recycled monomer product is described, wherein by addition of a diacid monomer to the recycled monomer product a monomer slurry is obtained which is maintained in liquid form and used for the polymerization of a polyester. Said recycled monomer product is obtained by depolymerization of a polyester from a waste stream with a diol monomer. The thus obtained depolymerization solution is mixed with water or an inert solvent to obtain a diluted solution, cooled to cause precipitation of the recycled monomer product including the condensation monomer and the precipitated recycled monomer product recovered therefrom.

[0010] The waste stream may comprise a liquifying contaminant, which is defined as substances which are solid at room temperature butliquid and not soluble in the depolymerization solution formed under the depolymerization conditions.

[0011] In WO 2023 / 217707 Al, in one embodiment it is suggested to divide the depolymerization solution into two portions while maintaining the liquifying contaminant in a liquid state, wherein said first portion contains liquifying contaminant and said second portion is essentially free of liquifying contaminant. The liquifying contaminant in said first portion is solidified by contact with a diol monomer, preferably water or an inert solvent as a cooling liquid and subsequently removed from the diluted solution in solid form.

[0012] While said solution allows for removal of solidified liquifying contaminants after cooling (which is not possible with the use of heat exchangers, since the liquifying contaminant would solidify at the heat exchanger and block it), it is not yet optimal. The use of water or an inert solvent as a cooling liquid requires a subsequent step of solvent separation, if the diol monomer (in the case of PET (polyethylene terephthalate) this is ethylene glycol (EG) ) is to be recovered, which is highly favorable or even necessary under economic and ecological considerations.

[0013] In WO 2023 / 217707 Al, as a theoretical alternative it is suggested, in addition to its use as a reactant for the depolymerization of a polyester, to use the diol monomer (such as ethylene glycol (EG) ) as cooling liquid. However, this would require the addition of fresh (pure) EG as a cooling liquid. Any recovery thereof would still require extensive purification, like distillation, from dissolved product and contaminants at the end of the process. Neither a direct feed-back loop nor the use of suchdiol as monomer for the subsequent production of a polyester is foreseen.

[0014] In WO 2023 / 083692 Al, a device and process for preparing a polyester depolymerisate is described, wherein liquid polyester depolymerisate is mixed with solid polyester recyclate and subsequently reacted with a depolymerizing agent such as a diol monomer. No separation of liquid contaminants by addition of a cooling liquid is described. Such a device does not allow the removal of liquifying contaminants in solid form, as the depolymerisate would solidify before the liquifying contaminants.

[0015] It was the problem of the present invention to provide an improved process which overcomes the disadvantages of the methods described above. This problem is solved by the process of the present invention.

[0016] In detail, the present invention provides a process for the preparation of a purified solution containing a polyester depolymerization product according to claim 1.

[0017] Specifically, the above problem is solved by a process for the preparation of a purified solution (PS) containing a polyester depolymerization product, said polyester depolymerization product having a repeat unit [-A' ' -B' ' ] with the formula [-O-R1-OOC-R2-CO-], and having 1 to 9 repeat units wherein

[0018] R1and R2are the same or different and are selected from the group consisting of aliphatic hydrocarbons containing 1 to 15 carbon atoms, aromatic hydrocarbons containing 1 to 3 aromatic rings, cyclic hydrocarbons containing 4 to 10 carbon atoms, and heterocyclic rings containing 1 to 3 oxygen atoms and 3 to 10 carbon atoms,

[0019] said method comprising the steps:al ) providing a waste stream (W) comprising

[0020] a polyester with the repeat unit [-A' ' -B' ' ] having the formula [ -O-R1-OOC-R2-CO- ], with more than 9 repeat units; and a liquifying contaminant at a concentration of 0.001 to 48% by weight, based on the entire amount of the waste stream, wherein the liquifying contaminant is defined as substances which are solid at room temperature but liquid and not soluble in the depolymerization solution formed in step a3) under the conditions of step a3),

[0021] a2 ) forming a blend comprising the waste stream (W) and at least one diol monomer HO-R1-OH (A), which is capable of reacting with the polyester,

[0022] a3) exposing the blend obtained in step a2 ) in a reaction vessel ( 1 ) to conditions suitable for at least partial depolymerization of the polyester resulting in a depolymerization solution (DPS) containing the polyester depolymerization product,

[0023] a4 ) mixing the depolymerization solution from step a3), said depolymerization solution having a temperature Tl, with a cooling liquid (C) having a temperature T2, wherein T2< T1, to obtain a diluted solution (DS) having a temperature T3, at which the liquifying contaminant is solidified, wherein T2< T3< T1, and

[0024] a5) removing solidified liquifying contaminant in solid form from the diluted solution (DS), so as to obtain the purified solution (PS) containing the polyester depolymerization product,

[0025] characterized in that the cooling liquid (C) added in step a4 ) is a portion of the purified solution (PS) containing the polyester depolymerization product obtained in step a5) that has been adjusted to the temperature T2.It has been found that the process for the preparation of a purified solution (PS) containing a polyester depolymerization product can be advantageously carried out if the cooling of the depolymerization solution containing the liquifying contaminant is performed using as a cooling liquid a portion of the purified solution (PS) containing the polyester depolymerization product that is obtained in the process of the invention.

[0026] This avoids the necessity of having to add fresh EG as a cooling liquid (with the disadvantage described above). The present invention also does not use recovered EG from the process of the invention, since that recovery would require extensive purification. Rather, it was found that without any need for purification, the purified solution (PS) can be used as such, as the cooling liquid.

[0027] It is an advantage of the present invention that the obtained purified solution (PS) can be directly used as a component for the manufacture of a polyester, together with the other component being a diacid monomer that is to be added to the purified solution (PS). No separation of polyester depolymerization product and diol monomer (such as EG) is necessary.

[0028] The following designations will be used herein for the condensation polymers, their depolymerization products and their monomers.

[0029] Monomer: A general term for building blocks of polymers. For condensation polymers, monomers comprise individual monomers, substituted monomers and condensation monomers.

[0030] Individual monomer: The basic building blocks of the polymer in unreacted form. According to the present invention, monomer A isa diol having the formula HO-R1-OH and monomer B is a diacid having the general formula HOOC-R2-COOH, wherein R1and R2throughout this specification are the same or different and are selected from the group consisting of aliphatic hydrocarbons containing 1 to 15 carbon atoms, aromatic hydrocarbons containing 1 to 3 aromatic rings, cyclic hydrocarbons containing 4 to 10 carbon atoms or heterocyclic rings containing 1 to 3 oxygen atoms and 3 to 10 carbon atoms. The diol monomer may be fresh diol and / or it may be obtained from any of the process steps for manufacturing a polyester.

[0031] Condensation monomer: A short condensation product from both individual monomers A and B, with the formula A'-B''-A', wherein A' and B' ’ have the below definitions. More specifically, the condensation monomer A'-B''-A' is HO-R1-OOC-R2-COO-R1-OH, wherein R1and R2are as defined above.

[0032] Reacted monomer: A building block of the polymer in reacted form in any larger molecule. Possible forms are A', A' ’, B' and B' ’, with A' being identical to H' -A' ’ and B' being identical to H' -B' '.

[0033] According to the present invention

[0034] an A' unit represents a reacted monomer A which is a diol with 1 reacted end group and one unreacted -OH end group and having the formula HO-R2-O-;

[0035] an A' ' unit represents a reacted monomer A which is a diol with 2 reacted end groups and having the formula -O-R2-O-,

[0036] the reacted A units represent the sum of all reacted monomer units A' and A' ’ and

[0037] the total A units represent the sum of all reacted and unreacted monomer units A, A' and A' ’.According to the present invention

[0038] a B' unit represents a reacted monomer B which is a diacid with 1 reacted end group and one unreacted -COOH end group and having the formula HOOC-R2-CO-;

[0039] a B' ' unit represents a reacted monomer B with 2 reacted end groups, preferably a diacid with 2 reacted end groups and having the formula -OC-R2-CO-, wherein

[0040] the reacted B units represent the sum of all reacted monomer units B' and B' ’ and

[0041] the total B units represent the sum of all reacted and unreacted monomer units B, B' and B' ’.

[0042] For example, the total B units is the total amount of B units in a given product and is the molar sum of all molecules containing a B unit multiplied by the number of B units in the respective molecules. For example, a product containing monomers B and A'-B''-A' as well as dimer A' -B' ’ -A’ ’ -B' ’ -A’ has a total amount of B units = mol B + 1 * mol A'-B''-A' + 2 * mol A' -B' ' -A' ' -B' ' -A'.

[0043] The following terms comprise the listed mole amount per substance:

[0044] IndiIndiMonomer Monomer Dimer vidual vidual A'-B'' A'-B''-A' A'-B''-A''-B''-A' monomer monomer

[0045] A B

[0046] Individual 1

[0047] monomer A

[0048] HO-Ri-O-H

[0049] Individual 1

[0050] monomer B

[0051] HOOC-R2-COOH

[0052] A' units 1 2 2

[0053] HO-R2-O- A' ' units 1

[0054] -O-R2-O- reacted A 1 2 3

[0055] units

[0056]

[0057] IndiIndiMonomer Monomer Dimer vidual vidual A'-B'' A'-B''-A' A'-B''-A''-B''-A' monomer monomer

[0058] A B

[0059] (A' + A" )

[0060] Total A 1 1 2 3

[0061] units (A +

[0062] A' + A" )

[0063] B' units 1

[0064] HOOC-R2-CO- B' ' units 1 2

[0065] -OC-R2-CO- reacted B 1 1 2

[0066] units

[0067] (B' + B" )

[0068] total B 1 1 1 2

[0069] units (B +

[0070] B' + B" )

[0071]

[0072] Repeat unit: A condensation product from one of each individual monomer A and B. Possible forms are -A' ' -B' ' - having the formula [ -O-R1-OOC-R2-CO- ], which would provide the repeating structure in the middle of a molecule, or A' -B' ' - and -B^ -A', which would provide the structure at the end of a molecule. A single repeat unit is also present in the condensation monomer A' -B'.

[0073] Dimer: A condensation product of both individual monomers with two repeat units. Possible linear forms are A' -B' ’ -A' ’ -B' ’ -A', B’ -A’ ’ -B’ and A' -B' ’ -A' ’ -B'. The condensation product B' -A' B' ' -A' ' -B' would be considered as a trimer and therefore part of the oligomers. A possible cyclic form is -A' ’ -B' ’ -A' ’ -B' ’ -, where each A’ ’ is linked to a B' ’.

[0074] Oligomer: A condensation product of both individual monomers A and B with several repeat units in the general linear form of E [-A' ' -B' ' ]n-E, where 3<= n <=9, -A' ' -B' ' - has the formula [-0-R1-OOC-R2-CO- ] and E = H', A' or B'.

[0075] A possible cyclic form is [ -A' ’ -B' ’ ]n-, where each A' ’ is linked to a B' ’ and where 3<= n <=9.

[0076] Polyester Depolymerization product: Any short chain product obtained by depolymerizing a polyester with a diol monomer, said polyester depolymerization product having the repeat unit [-A' B' ’ ] and having 1 to 9 repeat units. It comprises condensation monomer, dimers and / or oligomers thereof in their linear and / or cyclic form. It may comprise only one or multiple types of individual diol monomer A. It may comprise only one or multiple types of individual diacid monomer B.

[0077] Condensation Polymer: A condensation product of both individual monomers with a large number of repeat units in the general form of E [-A' ’ -B' ’ ]n— E, where n >9, preferably n>30 and most preferably n>50, where -A' ' -B' ' - has the formula [ -O-R1-OOC-R2-CO- ] and E = H', A' or B'. According to the present invention, the condensation polymer is a polyester.

[0078] Cooling liquid: The cooling liquid is based on diol monomer, HO-R2-OH. This means that the majority, preferably more than 80%, more preferably more than 90%, most preferably more than 95% by weight of the liquid components in the cooling liquid comprise diol monomer. Other liquid components may be liquid contaminants from the waste steam or reaction products thereof. Water may be present as a reaction product, especially if diol monomer recovered from a polyester manufacturing process is used. The cooling liquid may contain solids, especially if a slurry obtained from precipitated polyester depolymerization product or from adding a diacid monomer to the purified solution of the present inventionis used as cooling liquid. Solids may be dissolved and / or suspended in the cooling liquid. Neither the suspended nor the dissolved solids are considered as part of the liquid components.

[0079] Polyesters are obtained by a polycondensation reaction with elimination of a low molecular weight reaction product. The polycondensation can be effected directly between the monomers. The polycondensation may also be effected via an intermediate product, which is subsequently reacted by transesterification with elimination of a low molecular weight reaction product, or which is reacted by ring-opening polymerization.

[0080] The polyesters thus obtained have a substantially linear polymer chain. It is however possible for a small number of branches to form.

[0081] Preferred polyesters according to the present invention are thermoplastic polyesters.

[0082] Polyesters are polymers which are usually obtained by polycondensation from a diol component having the general formula

[0083] HO-R1-OH and a dicarboxylic acid component having the general formula HOOC-R2-COOH, where R1and R2are usually aliphatic hydrocarbons containing 1 to 15 carbon atoms, aromatic hydrocarbons containing 1 to 3 aromatic rings, cyclic hydrocarbons containing 4 to 10 carbon atoms or heterocyclic rings containing 1 to 3 oxygen atoms and 3 to 10 carbon atoms. Typically, linear or cyclic diol components and typically linear, aromatic, or heterocyclic dicarboxylic acid components are used. Instead of the dicarboxylic acid it is also possible to use its corresponding di-esters, typically its dimethyl ester. Preferred examples of such polyesters are polyethylene terephthalate (PET) which is typically obtained from terephthalic acid (TPA) and ethyleneglycol (EG), polybutylene terephthalate (PBT) obtained from terephthalic acid (TPA) and 1, 4-butylene diol (BD), polytrimethylene terephthalate (PTT) obtained from terephthalic acid (TPA) and 1, 3-propane diol (PD), polyethylene furanoate (PEF) obtained from 2, 5-furandicarboxylic acid (FDCA) and ethylene glycol (EG), polytrimethylene furanoate (PTF) obtained from 2, 5-furandicarboxylic acid (FDCA) and propane diol (PD), polybutylene succinate (PBS) obtained from succinic acid (SA) and butane 1, 4-diol (BD), polybutylene adipate (PBA) obtained from adipic acid (AdA) and 1, 4-butane diol (BD), polybutylene adipate-terephthalate (PBAT) obtained from adipic acid (AdA) terephthalic acid (TPA) and 1, 4-butane diol (BD) and polyethylene naphthalate (PEN) obtained from naphthalene-2, 6-dicarboxylic acid and ethylene glycol, where all of the above polyesters may be present in the form of a homopolymer or as copolymers.

[0084] The present invention describes a method to prepare polyesters by incorporating polyester depolymerization products. The polyester prepared therefrom and the polyester providing the source for the depolymerization products may be identical or may differ in composition. The differences in composition may result from the use of different monomers and / or from the use of different amounts of common monomers when preparing said polyester. The differences in composition may also result from blends of different polyesters. In accordance with the present invention, at least one common monomer is present in the polyester providing the source of the depolymerization products and the polyester prepared therefrom.

[0085] For example, a PET may be depolymerized using butane diol as a reaction partner, and the resulting polyester depolymerization product may be re-polymerized to form a PET / PBT copolymer. Al-ternatively, a PET copolymer with a high amount of diol comonomers may be depolymerized using ethylene glycol as a reaction partner, and the resulting polyester depolymerization product may be re-polymerized to form PET with a lower comonomer content.

[0086] Polyesters according to the present invention have a general structure comprising repeat units [A' ' -B' ' -] specifically having the formula [ -O-R1-OOC-R2-CO- ]. These polyesters can be recycled by depolymerization with the addition of a diol monomer A having the formula HO-R1-OH. The depolymerization results in a polyester depolymerization product comprising a condensation monomer, which as defined above is in the form of A'-B''-A' and specifically has the formula HO-R1-OOC-R2-COO-R1-OH or dimers and / or oligomers thereof.

[0087] According to the present invention, the polyester depolymerization product is obtained by depolymerization of a polyester that is present in a waste stream.

[0088] The waste stream of step al ) may be any stream which predominantly comprises polyester. It may further contain contaminants. The contaminants include solid substances which are mixed with the polyester particles. Typical are metal, paper or foreign plastic. The contaminants include solid or liquid substances adhering to the surface of the polyester particles. Typical are residues from a prior use, like sugar or edible oil, or from cross contamination during collection sorting and pre-cleaning, like sand, stones or washing chemicals. The contaminants further include substances inside the polyester particles. Typical are absorbed volatile substances from previous use, like aroma substances, household chemicals or solvents. Typical are also mixedcontaminants, like additives such as colorants, inorganic fillers or organic additive carriers. Typical are also mixed contaminants, like different polymers in polymer blends or blends with natural fibers such as cotton. The contaminants also include water and organic substances which adhere to the surface of the waste particles or which are absorbed by the waste particles.

[0089] The waste stream may result from post-industrial or post-consumer waste. Such waste may be in the form of articles, like containers or fabrics, or it may be in the form of intermediate products like sheets, fiber rolls or preforms for containers, or it may be in the form of raw materials like pellets or shredded solidified melt. The waste stream may have undergone pre-cleaning steps like optical sorting or separation by mechanical means such as density separation or screening to remove foreign polymers, and non-pol-ymeric substances.

[0090] The waste stream may have undergone pre-cleaning steps like washing with hot or cold water optionally containing caustic substances and / or detergents to remove surface contaminants.

[0091] The waste stream may have undergone pre-cleaning steps like drying at elevated temperatures to remove moisture and / or volatile organic contaminants.

[0092] The waste stream may be cut into particles, or it may be in the form of dust or powder. Typical particle sizes are in the range of 0.1mm up to several centimeters. For ease of handling particles above 1mm are preferred and to prevent non-dissolved particles to block pipes a size below 5cm especially below 3cm is preferred.According to the present invention the waste stream comprises liquifying contaminant. Already a very low level of liquifying contaminant is critical for cooling by the use of heat exchangers. For example, a process operating a waste stream containing lOppm of liquifying contaminant at lOOt / day using a heat exchanger will be faced with 1kg of liquifying contaminant per day. Assuming an even deposit layer of 1mm this has the potential to coat about one square meter of heat exchange area. This will cause frequent process interruptions for heat exchanger cleaning. Liquifying contaminant is defined as substances which are solid at room temperature but liquid and not soluble in the depolymerization solution formed in step a3) under the conditions of step a3). Liquifying contaminant is present at a concentration of 0.001% to 48% by weight, based on the entire amount of the waste stream. The meaning of "not soluble" refers to any part of a substance which is, given its amount, not dissolved. Minor portions which go into solution are not considered. Solidified liquifying contaminants may exhibit a stickiness temperature range where they appear mostly solid but tend to stick together and / or to metal surfaces under their own weight or under pressure resulting from handling and storing them. In this context, strong stickiness of solidified liquifying contaminants is defined where sticking occurs without applying external pressure. Typical liquifying contaminants are polyolefin polymers, such as LDPE or polyethylene copolymers, polyolefin waxes, such as slip agents, and fatty acids, such as stearic acid. Higher amounts of liquifying contaminant will not only cause frequent heat exchanger cleaning but will make the use of heat exchangers before the removal of liquifying contaminants close to impossible. Therefore, the process according to the present invention is most advantageous if the content of liquifying contaminant is at a concentration above 0.01%, more preferred above 0.1% and most preferably above 1%.According to a preferred embodiment of the present invention the waste stream may comprise solid contaminant. Solid contaminant is defined as substances which are solid and not soluble in the depolymerization solution formed in step a3) under the conditions of step a3). Solid contaminant may be present at a concentration of 0.01% to 48% by weight, based on the entire amount of the waste stream. The meaning of not soluble refers to any part of a substance which is, given its amount, not dissolved. Minor portions which go into solution are not considered. Preferably, the overall content of polyester is above 50%. The use of the preferred embodiment is most suitable if the content of liquifying plus solid contaminant is at a concentration above 0.1%, more preferred above 1% and most preferably above 5%.

[0093] Waste streams with high amounts of liquifying contaminant are for example polyester sheets with a polyolefin layer or a silicone release layer or polyester containers with polyolefin-based barrier layer such as EVOH.

[0094] Waste streams with high amounts of solid contaminant are for example polyester fibers mixed with non-melting fiber material like cotton. Other sources of polyester waste streams with high contaminant levels are mixed fractions which may result from cleaning steps in polymer sorting or washing facilities.

[0095] In step a2 ), said waste stream is blended with a depolymerizing agent, which according to the present invention is a diol monomer.

[0096] Forming the blend in step a2 ) comprises any form of mixing and mixing units that can be used to mix a typically solid or liquid waste stream and a typically liquid diol monomer. Alternatively, it comprises any form of mixing and mixing units that can be usedto mix a typically solid waste stream and a solid diol monomer. In both cases heating may be applied to facilitate the formation of the blend.

[0097] Typically, the waste stream is supplied to the mixing unit in a controlled amount. This may include any gravimetric or volumetric dosing unit, such as loss in weight feeders, belt scales or an air lock. The supply of the waste stream in solid form may comprise pneumatic conveying, screw conveying, belt conveying and / or gravimetric feed. An extruder with or without a dosing pump and or a melt filter may be used to supply the waste stream in liquid form. In this case it is preferable to supply the liquid waste stream at a position to the mixing unit which is below the fill level in the mixing unit to promote immediate contact between the waste stream and the diol. Preferably the supply of the liquid waste stream occurs through multiple openings, which provides a large surface contact area between the waste stream and the diol monomer. This is especially important if the melting point of the liquid waste stream is above the boiling temperature of the diol monomer.

[0098] According to the present invention at least one diol monomer HO-Rl-OH, which is capable of reacting with the polyester is used.

[0099] Typically, only one diol monomer is used. The use of different diol monomers will result in a mixed polyester depolymerization product, which may only be useful for special co-polyesters.

[0100] Nevertheless, any diol monomer may contain small amounts of impurities, like dimers thereof. Typically, the diol monomer is supplied to the mixing unit in a controlled amount. This may include any gravimetric or volumetric dosing unit. Alternatively, a weight or volume difference from a supply tank is used. Typically, the diol monomer is supplied in liquid form through a pump.According to the present invention, the diol monomer may be supplied in pure form or as part of a composition comprising said diol monomer. According to preferred embodiments of the present invention, the diol monomer may be supplied as part of the purified solution (PS) obtained by the process of the present invention.

[0101] The ratio of the solid waste stream and the diol monomer has a significant impact on the final composition of the polyester depolymerization product after depolymerization but also the economics of the recycling process. In a preferred embodiment the ratio of the sum of all diol monomers added in step a2 ) to the polyester repeat units contained in the waste stream from step al ) is in the range between 1: 1 and 10: 1, preferably equal or larger than 3: 1, more preferably more than 4: 1 and preferably below 8: 1 and more preferably below 6: 1, wherein the ratio is a molar ratio. In cases where a solution after depolymerization is used to supply the diol monomer, the content of diol monomer in the solution is estimated based on the assumption that the polyester has reacted with the diol monomer to form a dimer in the form of A' -B' ' -A' ' -B' ' -A'.

[0102] At the same time, the ratio of the volume flow rates has to be considered. Depending on its bulk density the added waste stream has a void volume, which needs to be filled by solution to allow the waste stream to be submerged in the solution. While a batch process, where the total amount of the waste stream is added at the beginning, may require a large excess of added solution, a sequential addition of the waste stream over time allows to reduce the initially added solution amount. In a continuous process the solution in the depolymerization reactor would typically exceed the volume of the added waste stream, making theratio of the added streams less critical. In general, a weight ratio of added waste stream to added liquid stream should be above 1: 1 and preferably above 1.5: 1.

[0103] The blend may further comprise a catalyst to facilitate the subsequent depolymerization reaction. Such a catalyst may be in the form of a metal salt or in the form of an organic substance. Also, organic metal complexes can be used. The catalyst may be added in solid or liquid form as a pure substance or in solution. When a solution is used the diol monomer is the most suitable solvent.

[0104] Forming the blend may be accomplished in continuous fashion or by preparing individual batches. One option is to use an agitated vessel to form the blend. Depending on the ratio of liquid to solid and the bulk density of the solids the solids may not be fully submerged in the liquid. In that case forming the blend may require some depolymerization and partial dissolution of solids in the liquid before a homogeneous blend is formed. In that case step a2 ) and a3) overlap. The steps a2 ) and a3) also overlap in a continuous process where diol monomer and the waste stream are supplied to depolymerization reactor in which depolymerization is already ongoing. Such a procedure is explained in US-4, 609, 680. Another option is to use an extruder to melt the polyester and mix it with a diol monomer.

[0105] Step a3) comprises the depolymerization of the blend obtained in step a2 ). The conditions suitable for depolymerization of the polyester in the waste stream are well known in the industry. As an example, various methods for the depolymerization of PET are described in " Recycling of Polyethylene Terephthalate Bottles; Elsevier; 1sted. 2018, Edited by Sabu Thomas". According to the present invention, depolymerization conditions must be sufficient to ob-tain at least partial depolymerization, resulting in a depolymerization solution containing a polyester depolymerization product with a repeat unit [-A' ' -B' ' ] having the formula [ -O-R1-OOC-R2-CO- ] and having 1 to 9 repeat units.

[0106] As indicated before, the mixing of step a2 ) and the depolymerization of step a3) may overlap as depolymerization may already start during mixing. In one preferred embodiment, the diol monomer may be supplied as part of the purified solution (PS) obtained by the process of the present invention. The purified solution (PS) may be heated to facilitate the subsequent depolymerization. In said embodiment depolymerization may start upon addition of the purified solution (PS).

[0107] In another embodiment, hot diol monomer is mixed with the waste stream to preheat the waste stream to a temperature sufficient to initiate depolymerization. A suitable temperature is typically above 130°C and at least 20°C below the boiling temperature of the diol monomer.

[0108] In any case the final level of depolymerization is obtained in step a3).

[0109] Depolymerization occurs in a reaction vessel. One option is to use an agitated vessel for depolymerization. In a batch process, this may be the same vessel as has been used in step a2 ). In a continuous process, a separate agitated vessel or a series of agitated vessels is preferred.

[0110] Alternatively, a pipe reactor may be used instead of one or several of the agitated vessels. Typically, the reaction vessel comprises heating means, such as mantle heating, internal heating coils oran external heat exchanger through which a part of the depolymerization solution is pumped and returned to the vessel.

[0111] The vessel is heated to conditions suitable for the depolymerization of the polyester. Typically, a temperature of 170°C has to be exceeded to reach sufficient depolymerization. Preferably the temperature is raised up to the boiling temperature of the diol monomer. The diol monomer may contain other liquids. As a consequence, the boiling temperature may be below the boiling temperature of the diol monomer. As the other liquids evaporate from the depolymerization solution, the boiling temperature increases. As recycled polyester depolymerization product is formed and dissolved in the diol monomer, the boiling temperature of the diol monomer increases above its initial boiling temperature. Preferably sufficient heating is provided to maintain boiling. The reaction vessel is typically operated with a pressure range of 500mbar to 5bar. It is however preferred to operate the reaction vessel at approximately atmospheric pressure in the range of 1bar ± 100mbar. Especially preferred is to operate the reaction vessel at slight overpressure, up to 100mbar, to allow the transfer of evaporated liquids to subsequent process steps. The pressures refer to absolute pressure if not noted differently.

[0112] In a series of reaction vessels, temperature and pressure can change from one vessel to the next. Especially if an extruder is used in step a2 ), higher temperatures and pressures may be initially used. However, according to the present invention such an extruded blend would be subsequently transferred to a reactor within the above-mentioned specifications.

[0113] The depolymerization is continued until a depolymerization solution has formed. Except for some contaminants the waste stream should be fully dissolved in the depolymerization solution. Longreaction times at high temperature should be avoided as this causes the formation of side products, like the formation of dimers of the diol monomer. The residence time for the steps a2 ) and a3 ) together is typically in the range of 20 minutes to 6 hours. In cases of step a3 ) occurring at approximately ambient pressure with boiling diol monomer, residence times in the range of 1 to 5 hours are preferred. In cases where the waste stream is preheated as described above, residence times including such preheating may reach up to 24 hours.

[0114] According to the present invention, it is preferred that between steps a3) and a4 ) a purification step is carried out to remove solid contaminants that are derived from the waste stream (W). Preferably, said purification step is a filtration, more preferably a filtration using a filter with a screen opening size of less than 20µm, more preferably less than 10µm. For this purpose, any conventional filter may be used. Typical suitable filtration equipment includes bag filters or basket filters, also called candle filters.

[0115] In step a4 ) the depolymerization solution from step a3) is mixed with a cooling liquid to obtain a diluted solution. Any mixing unit suitable to mix two different liquids may be used. In a batch process, this may be the same vessel as has been used in step a3). In a continuous process, a separate unit is preferred. The mixing unit may comprise additional cooling means, such as mantle cooling, to support the cooling, which allows reducing the amount of cooling liquid.

[0116] The amount of cooling liquid compared to the amount of depolymerization solution is in the range between 5: 1 and 1: 2, preferably below 3: 1, more preferably below 2.5: 1, and preferably above 1: 1,more preferably above 1: 1.3. The mixing ratio is expressed as weight ratio.

[0117] The mixing may comprise adding all cooling liquid at one position into the full amount of the depolymerization solution. The mixing may also involve adding parts of the cooling liquid at different positions. The mixing may comprise mixing all depolymerization solution with only a part of the cooling liquid and a subsequent mixing with the rest of the cooling liquid. In any case where the distinction can be made, especially in batch processes, it is preferred to add cooling liquid into the depolymerization solution and not to add the depolymerization solution into the cooling liquid. This prevents an initial super cooling of parts of the depolymerization solution.

[0118] When operating in continuous mode, in a preferred embodiment of the present invention the addition of cooling liquid and depolymerization solution is performed simultaneously into an agitated mixing vessel.

[0119] In another preferred embodiment, the addition of cooling liquid is performed in such a way that depolymerization solution flows through a pipe and cooling liquid is injected into the pipe.

[0120] According to the present invention the flows and the temperatures of the two liquid streams should be adjusted before mixing in such a way that the resulting diluted solution (DS) reaches a temperature T3 at which the liquifying contaminant is solidified. In case of a depolymerization solution resulting from polyethylene terephthalate and ethylene glycol, a temperature of the diluted solution above 60°C and below 110°C is preferred. More preferred is a temperature above 70°C and / or below 100°C.The depolymerization solution from step a3) has, when leaving the reactor vessel used in step a3), a temperature T5. The temperature T5 can be expressed in relation to the boiling point TBof the monomer diol used as depolymerizing agent as follows:

[0121] TB- 30°C ≤ T5 ≤ TB+ 50°C, preferably TB- 10°C ≤ T5 ≤ TB+ 10°C.

[0122] For example, when the diol monomer is ethylene glycol (EG), preferably T5 = 170-250°C, more preferably 190-205°C.

[0123] While in principle the depolymerization solution (DPS) could still have a temperature T5 when entering step a4 ) (thus T5 being identical with Tl ), according to the present invention it is preferred that between steps a3) and a4 ) the depolymerization solution (DPS) containing the polyester depolymerization product is cooled from the temperature T5 to the temperature Tl, wherein T5 ≥ T1 ≥ T5 -50°C, preferably T5 ≥ T1 ≥ T5 -30°C.

[0124] For example, when the diol monomer is ethylene glycol (EG), preferably T1 = 150-210°C, more preferably 170-190°C.

[0125] The cooling liquid introduced into step a4 ) has a temperature T2, wherein T2< T1. According to the present invention, it is preferred that T2 = 10-60°C, more preferably above 25°C, especially preferred above 30°C and more preferably below 50°C, especially preferred below 45°C.

[0126] Step a4 ) is carried out such as to obtain a diluted solution (DS) having a temperature T3 at which the liquifying contaminant is solidified, wherein T2< T3< T1.

[0127] It should be noted that T2 and T3 are independent from the boiling point of the diol monomer that is used in the process of theinvention. T3 depends on the temperature at which the liquifying contaminants solidify. Typical liquifying contaminants such as polyolefins require cooling below 110°C. For some low melting polyolefin copolymers temperatures as low as 80°C may be required. T2 can be selected depending on the amount of cooling liquid that is to be added in step a4 ). If the cooling liquid has a higher temperature, more of the cooling liquid has to be added than if the cooling liquid has a lower temperature.

[0128] In step a5), solidified liquifying contaminant in solid form is removed from the diluted solution (DS), so as to obtain the purified solution (PS) containing the polyester depolymerization product.

[0129] The solidified liquifying contaminant is preferably removed by a screen or filter, which allows the solution to pass through but retains the majority of the liquifying contaminant in solid form. To facilitate the cleaning of the screen it is desirable to reduce the temperature sufficiently to prevent the liquifying contaminant from sticking on the screen. The screen openings have to be sufficiently wide to allow small particles of precipitated polyester depolymerization products or of dicarboxylic acid to pass through the screen if such particles are present. Typically screen openings above 100pm, preferably above 300pm, more preferably above 1mm are used. Preferably a cleaning liquid, typically the diol monomer, is used to remove precipitated polyester depolymerization product from the screen or filter and / or from the liquifying contaminant in solid form. Optionally a removal of diol monomer and polyester depolymerization product is performed once the liquifying contaminant in solid form has been removed from unit used for separating the liquifying contaminant in solid form.In an embodiment of the present invention without a purification step to remove solid contaminants between steps a3) and a4 ) or in an embodiment where only course filtration was used, solid contaminant may be removed from the diluted solution together with the liquifying contaminant.

[0130] Any removed solid particles typically contain residues of the depolymerization solution. It is therefore preferred to recover as much of the solution as possible. This may be done by a flow of air or a washing solution, preferably diol monomer.

[0131] The advantage of such a combined removal is the flexibility to operate the system with very different waste streams without the need to configure the system specifically for those waste streams. A further advantage is the single waste stream, which facilitates handling and solution recovery.

[0132] According to a preferred embodiment of the present invention the purified solution or a portion thereof undergoes an additional purification step to remove solid contaminants. Preferably, said additional purification step is a filtration, more preferably a filtration using a filter with a screen opening size of less than 20µm, more preferably less than 10µm. For this purpose, any conventional filter may be used. Typical suitable filtration equipment includes bag filters or basket filters, also called candle filters.

[0133] According to a preferred embodiment of the present invention, the blend formed in step a2 ) comprises functionalized magnetic particles, and the purified solution or a portion thereof undergoes an additional purification step to remove at least a part of said magnetic particles.According to a preferred embodiment of the present invention the purified solution or a portion thereof undergoes an additional purification step by contact with an absorption material. An absorption material is selected that is capable of reducing the amount of contaminants, such as metal ions, colorants or other organic substances which remain dissolved in the purified solution and differ in their composition from the repeat unit of the polyester introduced in step al ). Such absorption materials are known. As an example, activated carbon or ion exchange resins may be mentioned. Adsorption material may be present as fixed bed through which the purified solution is passed. In this case it is preferred to have solid contaminant removal upstream of the adsorption step. This prevents contamination of the fixed adsorption material bed with solid contaminants. Adsorption material may be present as powdered or granular material dispersed in the purified solution. In this case it is preferred to have solid contaminant removal downstream of the of the adsorption step. This allows to have a combined separation step for the solid contaminants and the adsorption material. If such a separation is performed by filtration, a filter aid may be incorporated.

[0134] Optionally the purified solution or a portion thereof that is directed to any additional purification step is heated to a temperature where preferably all precipitated polyester depolymerization product is dissolved. This succession of steps ( first removing liquifying contaminants at a lower temperature and then removing solid and / or dissolved contaminants at a higher temperature) has the advantage that the removal of these contaminants is not negatively impacted by the liquifying contaminants or precipitated polyester depolymerization product.The cooling liquid added into step a4 ) is or comprises a portion of the purified solution (PS) containing the polyester depolymerization product that is obtained in step a5).

[0135] In a first embodiment, a portion of the purified solution (PS) containing the polyester depolymerization product obtained in step a5) is transferred back into step a4 ). Since the diluted solution (DS) obtained in step a4 ) has a temperature T3 at which the liquifying contaminant is solidified, wherein T2< T3< T1, the portion of the purified solution (PS) containing the polyester depolymerization product that is to be used as a cooling liquid will typically have a temperature higher than T2. Thus, before being introduced into step a4 ) as cooling liquid, the temperature of said portion of the purified solution (PS) containing the polyester depolymerization product has to be adjusted to the temperature T2. Due to the fact that the liquifying contaminants have been removed, this can be done by conventional cooling units, such as heat exchangers.

[0136] According to a preferred embodiment of the present invention, before being added into step a4 ), the cooling liquid is brought into contact with an absorption material. An absorption material is selected that is capable of reducing the amount of contaminants, such as metal ions, colorants or other organic substances which remain dissolved in the cooling liquid and differ in their composition from the repeat unit of the polyester introduced in step al ). Such absorption materials are known. As an example, activated carbon or ion exchange resins may be mentioned. It has to be understood, that such contaminant removal is selective to certain types of contaminants and will not result in pure diol monomer. Even after such contaminant removal, a diol-based solution of polyester depolymerization product will be used as a cooling liquid.According to a preferred embodiment of the present invention, the portion of the purified solution (PS) containing the polyester depolymerization product that is to be used as the cooling liquid (C) in step a4 ) is obtained by precipitating polyester depolymerization product, and subsequently separating purified solution (PS), preferably by a mechanical separation, into a fraction rich in the polyester depolymerization product and a fraction rich in the diol monomer, wherein at least a part of the fraction rich in the diol monomer is the portion to be used as the cooling liquid (C) in step a4 ). Precipitation of polyester depolymerization product may be due to the cooling in step a4 ) or due to cooling purified solution (PS) containing the polyester depolymerization product obtained in step a5). Optionally, the fraction rich in diol monomer may be additionally cooled before being used as the cooling liquid (C) in step a4 ).

[0137] The option with additional cooling after separation provides the advantage that a depolymerization solution with a high solidification temperature (and therefore a low molar ratio EG: PET) can be used in the steps leading to and including separation and that only the portion rich in diol monomer, and therefore a lower solidification temperature, is cooled to the temperature required to be used as cooling liquid in step a4 ).

[0138] The separation unit suitable for the mechanical separation described above may be any unit that separates particles by any method suitable for a mechanical solid liquid separation. This includes filtration, however preferred are decanters, centrifuges, hydro cyclones or simple sedimentation tanks. Preferred are dynamic separation units that allow a separation in less than 5 minutes, like decanters, centrifuges or hydro cyclones. Not included are septation units based on thermal methods where the diol monomer is evaporated. The advantage of a mechanical separation isthe removal of contaminants which are soluble in the solution and therefore are directed away from the fraction rich in the polyester depolymerization product. The separation may be performed in batch or in continuous mode. Where no suitable continuous equipment is available, alternating batch systems will be used.

[0139] It has to be understood, that such separation is limited to the solubility of the polyester depolymerization product and will not result in pure diol monomer. At the same time the yield of the fraction rich in polyester depolymerization product will be low at the beginning. However, as the cooling liquid returns polyester depolymerization product, its concentration in the diluted solution will increase and eventually reach an equilibrium. Even after such increase in concentration, the fraction rich in the diol monomer will be used as a cooling liquid.

[0140] Once this equilibrium is reached, the amount of polyester depolymerization product in the fraction rich in polyester depolymerization product will correspond to the supplied input polyester amount. The solid content in the fraction rich in polyester depolymerization product may be so high, that it is provided from the separation step in solid or gel like, near solid consistency. In this case the fraction rich in polyester depolymerization product will be heated to obtain a liquid, pumpable solution.

[0141] Thus, in this embodiment the purified solution (PS) from step a5) is cooled. Any cooling unit suitable to cool a liquid and initiate precipitation of a dissolved solid may be used. Typically, an agitated vessel would be used. Typically, the vessel comprises cooling means, such as mantle cooling, internal cooling coils or an external heat exchanger through which a part of the diluted solution is pumped and returned to the vessel. Alternatively, at least a part of the cooling may occur in a plate or pipe heatexchanger. Optionally, a scraped wall heat exchanger is used to prevent that polyester depolymerization product deposits on cold surfaces.

[0142] Cooling must be sufficient to reach the predetermined temperature T2. However, cooling must maintain the diluted solution in liquid pumpable form. It is therefore important to thoroughly agitate the purified solution (PS) during cooling to prevent the formation of a gel like near solid consistency.

[0143] Typically, after separation the fraction rich in the diol monomer to be used as the cooling liquid (C) in step a4 ) has a temperature T4, wherein T4 = T2 ± 20°C, preferably T4 = T2 ± 10°C. This is sufficiently similar to T2, so that in a preferred embodiment an additional cooling step from T4 to T2 is not necessary, before the cooling liquid enters step a4 ).

[0144] In another preferred embodiment of the present invention, another portion of the purified solution (PS) containing the polyester depolymerization product obtained in step a5) is added into step a2 ). Said portion is a liquid stream, wherein the liquid stream comprises polyester depolymerization product and diol monomer.

[0145] In said embodiment, it may not be necessary to add fresh diol monomer into step a2 ) for the subsequent depolymerization in step aS) in the reaction vessel. It may, however, be advantageous to add fresh diol monomer into step a4 ) to adjust the amount of diol monomer in the process cycle.

[0146] In another embodiment of the present invention, the portion of the purified solution (PS) containing the polyester depolymerization product obtained in step a5) is present in a slurry thatis obtained by adding at least one diacid monomer (B) having the formula HOOC-R2-COOH to the purified solution of step a4 ) above. This will be explained in detail below.

[0147] The present invention is furthermore related to a process for the preparation of a polyester with a repeat unit [-A' ' -B' ' ] having the formula [ -O-R1-OOC-R2-CO- ], comprising the steps: a) providing a purified solution (PS) containing a polyester depolymerization product by the process according to the present invention,

[0148] b) adding at least one diacid monomer (B) having the formula HOOC-R2-COOH to the purified solution of step a), to obtain a slurry ( S ), and

[0149] c) using the slurry (S) from step b) for the polymerization of a polyester with the repeat unit [-A' ' -B' ' ] having the formula [ -O-R1-OOC-R2-CO- ],

[0150] wherein R1and R2are the same or different and are selected from the group consisting of aliphatic hydrocarbons containing 1 to 15 carbon atoms, aromatic hydrocarbons containing 1 to 3 aromatic rings, cyclic hydrocarbons containing 4 to 10 carbon atoms, and heterocyclic rings containing 1 to 3 oxygen atoms and 3 to 10 carbon atoms.

[0151] The purified solution (PS) containing a polyester depolymerization product can be supplied at any temperature. The temperature of the purified solution (PS) is preferably sufficiently high to assure a liquid, pumpable solution to prevent unwanted solidification. As explained before, agitation may be required to maintain such liquid, pumpable conditions. It is also preferable to keep the purified solution (PS) at a temperature below the melting temperature of the polyester to be obtained from the purified solution (PS). As the purified solution (PS) is used to prepare a slurry, whichis sensitive to thermo-oxidative degradation, it is preferable to maintain the temperature as low as possible.

[0152] According to the present invention, a diacid monomer B having the formula HOOC-R2-COOH is added to the polyester depolymerization product. The diacid monomer B may be added as a solid, preferably as a powder or fine granules. Typical particle sizes of the diacid monomer B to be used according to the present invention are in the range of 0.1 to 2000 pm, preferably 0. 5 to 500 pm, while the median particle size is preferably in the range of 10 to 300 pm, preferably in the range of 30 to 200 pm. The median particle size (also called D50value) is the particle size from which half of the particles are smaller and half are larger.

[0153] Alternatively, a diacid monomer B having the formula HOOC-R2-COOH may be added to the purified solution (PS) in a form dispersed in a liquid, like diol monomer. However, the amount of liquid should be limited as excessive amounts of diol have to be evaporated before or during subsequent polymerization of the polyester. According to a preferred embodiment of the present invention, the diacid monomer B having the formula HOOC-R2-COOH which is used to prepare a slurry is added without diol or with an amount of diol below the amount of diacid monomer B, preferably below 80% of the amount of diacid monomer B, wherein the calculation is based on the mole amounts of the respective components.

[0154] The diacid monomer B having the formula HOOC-R2-COOH should be added to the polyester depolymerization product in such a way that the polyester depolymerization product stays above its solidification temperature. Therefore, the diacid monomer B is preferably either heated above the solidification temperature of the polyester depolymerization product or, if added at a lower temperature,the polyester depolymerization product is heated sufficiently to prevent its solidification.

[0155] As the diacid monomer B is not soluble or only partially soluble in the purified solution (PS) containing the polyester depolymerization product, a slurry is formed where solid particles of diacid monomer B are dispersed in the purified solution (PS) containing the polyester depolymerization product. A liquid where the diacid monomer B is reacted with the polyester depolymerization product and / or the diol monomer A and therefore fully dissolves in the solution is not considered a slurry anymore.

[0156] The purified solution (PS) containing the polyester depolymerization product and the diacid monomer B should be sufficiently agitated to form a homogeneous slurry. The formation of agglomerates should be avoided.

[0157] According to the present invention, the amount of added diacid monomer B having the formula HOOC-R2-COOH depends on the amount of total B units (-OC-R2-CO-) and A units (-O-R1-O-) in the purified solution (PS) containing the polyester depolymerization product, which results from the amount of diol monomer A added in the steps a2 ) to a4 ), since at least a part of said diol monomer A is foreseen as a reagent in the subsequent polymerization and thus should form part of the resulting polyester.

[0158] The diacid monomer B having the formula HOOC-R2-COOH is preferably added in such a way that after its addition the slurry has a mole ratio of total A units (-O-R2-O-) to total B units (-OC-R2-CO-) in the range of 3: 1 to 1: 1, preferably below than 2: 1, most preferably below 1. 6: 1 and preferably above 1.05: 1. The total B units is calculated as described in the definitions and includes the B units derived from the added monomer B and the B units derived from thepolyester depolymerization product. The total A units is calculated as described in the definitions and includes the A units derived from the monomer A in the depolymerization solution and the A units derived from the polyester depolymerization product and optionally any additionally added monomer A.

[0159] If the ratio of total A units (-O-R1-O-) to total B units (-OC-R2-CO-) in the slurry is high, then a high amount of individual diol monomer A specifically having the formula HO-R1-OH has to be evaporated during the preparation of the polyester.

[0160] A person skilled in the art will understand that the parameters of mole ratio for depolymerization, mixing ratio for cooling, temperature of the depolymerization solution, temperature of the cooling liquid, solidification temperature of the liquifying contaminant and solidification temperature of the purified solution are linked and may require adjustments to obtain optimum conditions for the performance of the present invention. As a result of this optimization a purified solution will be obtained, which has a certain ratio of diol monomer A to polyester repeat units. According to the present invention the solution having this ratio of diol monomer A to polyester repeat units is directed to the process of polymerization, where diacid monomer is added as defined above. A person skilled in the art will understand that the ratios between diol monomer A and diacid monomer B as well as polyester repeat units to the monomers determines the content of recycled polyester in the final polyester. This content is, however, also influenced by the evaporation of diol monomer A during polymerization. While some evaporation is typical in the polymerization processes of polyesters, it is energy intensive and therefore should be limited.

[0161] Therefore, according to a particularly preferred embodiment, the present invention is performed in a way that the ratio of addedpolyester to the final polyester is higher than 10%, preferably higher than 15% and most preferably higher than 19%.

[0162] According to said particularly preferred embodiment, it is further preferred that the majority, more preferably above 80%, of the pure diol monomer A that is added to the steps a2 ) to a4 ) is directed towards re-polymerization of the final polyester in step c). In this context diol monomer losses (diol monomer that does not become part of the purified solution) are deducted from the added amount.

[0163] According to said particularly preferred embodiment, it is further preferred that evaporation of diol monomer A from the process to manufacture the final polyester is below a molar ratio of evaporated diol monomer A to added polyester repeat units of 3: 1, and preferably below 2: 1.

[0164] According to said particularly preferred embodiment, it is further preferred that the ratio of the sum of all diol monomers added in step a2 ) to the polyester repeat units contained in the waste stream from step al ) is in the range between 1: 1 and 10: 1, with the more preferred ranges being as described above.

[0165] According to said particularly preferred embodiment, it is further preferred that the amount of cooling liquid compared to the amount of depolymerization solution is in the range between 5: 1 and 1: 2 with the more preferred ranges as described above.

[0166] According to said particularly preferred embodiment, it is further preferred that the slurry has a mole ratio of total A units (-O-R1-O-) to total B units (-OC-R2-CO-) in the range of 3: 1 to 1: 1 with the more preferred ranges as described above.According to the present invention, the slurry described above is used for the polymerization of a polyester.

[0167] According to one embodiment of the present invention, the slurry is not directly transferred into a unit for polymerization of a polyester. Rather, between steps b) and c), the slurry (S) is reintroduced into step a4 ) of the process of the invention, as the cooling liquid (C). In said embodiment, the purified solution (PS) obtained in step a5) of the process of the present invention is inserted in the slurry formation unit, optionally after having been treated in a cooling unit and / or a second separation unit discussed below, where it is blended with the diacid monomer B. Said slurry contains at least a portion of the purified solution (PS) and is transferred back into a mixing unit, where step a4 ) is carried out. Optionally, said slurry may be cooled in a cooling unit before being transferred back into a mixing unit where step a4 ) is carried out.

[0168] In this embodiment, the slurry is subj ected to one or more cycles of steps a4 ) and a5), before it is transferred into a unit for polymerization of a polyester.

[0169] The preparation of a slurry by adding diacid monomer B may be performed in two steps, where in a first step a part of the diacid monomer B is added to the purified solution, which is subsequently used as cooling liquid, and in a second step a further part of the diacid monomer B is added to the slurry that is subsequently used for polymerization.

[0170] The preparation of polyesters has been well described. Various methods for the preparation of polyesters are described in " Modern Polyesters; Wiley Series in polymer Science; 2003; Edited by John Scheirs" (typical examples in chapters 2, 8, 9 and 11 ).Typical preparation processes comprise the direct reaction of equal amounts of individual monomers, leading to polyesters with the repeat unit structure [A' ' -B^ - specifically having the formula [ -O-R2-OOC-R2-CO- ]nwhich may be terminated by either A' (HO-R2-O-) and / or B' units ( -OC-R2-COOH). During the reaction, low molecular weight reaction products may form which have to be removed by evaporation. When using a purified solution (PS) according to the present invention, optionally containing a diacid monomer, the amount of diacid monomer has to be controlled in such a way that on a molar level equal amounts to diol monomer are present.

[0171] Other, so called two step, processes use individual diacid monomer B (HOOC-R2-COOH) and an excess of individual diol monomer A (HO-R2-OH) in a first step to form a prepolymer with the repeat unit structure [A'

[0172]

[0173] specifically having the formula [-O-R1-OOC-R2-CO-]n, where n is a small number of preferably less than 20 and which is mostly terminated by A' units (HO-R2-O-). During the reaction, low molecular weight reaction products may form, which have to be removed by evaporation.

[0174] In a second step, the prepolymer continues to react leading to polyesters with the repeat unit structure [A' ' -B^ - specifically having the formula [ -O-R2-OOC-R2-CO- ]n, which may be terminated by either A' (HO-R2-O-) and / or B' units ( -OC-R2-COOH). Excess individual diol monomer A (HO-R2-OH) is removed by evaporation during the second stage. When using a purified solution (PS) according to the present invention, optionally containing a diacid monomer, the amount of diacid monomer has to be controlled in such a way that on a molar level an excess of diol monomer is present.

[0175] According to one embodiment of the present invention, in step c)cl ) the slurry (S) is polymerized by melt phase polymerization to obtain a polyester polymer having a molecular weight below an intended molecular weight, and

[0176] c2 ) subsequently said polyester polymer is treated in the presence of a process gas at a temperature below its crystalline melting point to promote esterification and / or transesterification reactions, thereby increasing the molecular weight of the polyester,

[0177] wherein side products from the esterification and / or transesterification reactions are transferred into the process gas, and said process gas is subsequently purified in a purification step using a liquid adsorption media, and the purified process gas is reentered into step c2 ), and

[0178] the liquid adsorption media comprises a diol monomer which is reintroduced into step a4 ) of the process of the present invention. In step cl ), a polyester polymer is obtained having a molecular weight below an intended molecular weight. It is known that there are limitations on increasing the molecular weight of a polyester during melt phase polymerization, due to an unwanted degree of side reaction occurring during prolonged melt phase polymerization, which lead to a contamination of the polyester. Typically, melt phase polymerization is only carried out until a certain molecular weight has been reached. In order to increase the molecular weight of the thus obtained polyester to an intended level, in a second step c2 ) a solid-state post condensation (SSP) may be carried out using a heated process gas, such as nitrogen (N2). This is described, for example, in " Modern Polyesters; Wiley Series in polymer Science; 2003; Edited by John Scheirs".

[0179] In said embodiment, the side products that are generated during the SSP reaction are transferred from the polyester to the process gas. Said side products typically comprise diol monomer A, which may be reused. Thus, in a preferred embodiment the process gas maybe cleaned in order to recover at least a part of said side products and reintroduce them into step a4) of the process of the present invention. The purified process gas may be reintroduced into step c2 ) described above.

[0180] Cleaning of a process gas from SSP reactions is known in the art. Preferably, the cleaning of the process gas may be carried out with a liquid adsorption medium, preferably ethylene glycol (e. g. EP 1 789 469 Bl, section

[0083] ).

[0181] Many polyesters have at least one individual monomer A or B which is a liquid at ambient conditions. This allows to feed the individual monomers as a liquid to the polyester polymerization. If one monomer is liquid and a second monomer is solid, the solid monomer may be dispersed in the liquid monomer, forming a slurry of individual monomers, which is fed to the polyester polymerization. Typically, the diol, individual monomer A (HO-Rl-OH), is a liquid.

[0182] In this case another advantage of the present invention becomes obvious when looking at the liquid: solid ratio of a slurry. Whereas in the manufacture of polyester with a mole ratio liquid diol monomer A to solid diacid monomer B in the range of 1: 1 up to 1.5: 1 the liquid: solid ratio will also be 1: 1 up to 1.5: 1 (on a molar basis), according to the present invention the depolymerized polyester will become part of the liquid. For the manufacture of polyester with a mole ratio in the range of 1: 1 up to 1.5: 1 the liquid: solid ratio will be higher than 1: 1 up to 1.5: 1, which allows to reduce the excess of liquid diol monomer A that has to be added to the slurry preparation.A conventional plant designed to prepare a polyester from its individual monomers A and B therefore comprises a unit configured to prepare a slurry from individual monomers A and B. This slurry preparation unit typically has associated supply units which allow providing individual monomer A in liquid form and individual monomer B in solid form. The resulting slurry is then fed to the subsequent step of polyester polymerization.

[0183] It is therefore desirable to also provide the purified solution in liquid form to the polyester polymerization. However, in contrast to conventional plants, the purified solution contains dissolved polyester depolymerization product, which increases the viscosity of the diol monomer A on which the purified solution is based and has the tendency to obtain a gel like near solid consistency. The slurry needs to be maintained in a pumpable, liquid state above its solidification temperature. Typically, the slurry should be at a temperature at or above 30°C up to 200°C, preferably at or above 40°C, more preferably at or above 60°C, preferably below 160°C and more preferably below 140°C when feeding to polyester polymerization.

[0184] Therefore, it is preferable to maintain the unit for the preparation of the slurry at a temperature at or above 30°C up to 200°C, preferably at or above 40°C, more preferably at or above 60°C, preferably below 160°C and more preferably below 140°C. To maintain that required temperature, the unit for the preparation of the slurry is typically equipped with heating means, which are sufficient to maintain a temperature at or above 30°C up to 200°C, preferably at or above 40°C, more preferably at or above 60°C, preferably below 160°C and more preferably below 140°C.

[0185] A supply unit is required which allows to feed the slurry containing the polyester depolymerization product in liquid form at atemperature above its solidification temperature, which requires temperatures at or above 30°C up to 200°C, preferably at or above 40°C, more preferably at or above 60°C. The supply unit for the slurry may be any unit that allows providing the slurry in controlled amounts, while maintaining the slurry containing the polyester depolymerization product in liquid form. Examples are dosing pumps.

[0186] The slurry may contain additives such as catalysts, colorants, anti-oxidants, stabilizers or inorganic fillers. These additives may be added during the production of the polyester depolymerization product. These additives may also be added to the stream of polyester depolymerization product or to the stream of diacid monomer B (HOOC-R2-COOH) entering the slurry preparation unit. Alternatively, the additives may also be added to the slurry. The additives may be added in pure form, as a blend of additives or together with a liquid. Typically, such additives are dissolved or dispersed in individual monomer A (HO-R1-OH).

[0187] After slurry preparation, the polymerization process of the polyester commences identical or at least very similar to processes known from virgin polymer polymerization. Small differences may result from different mole ratios which influence the evaporation of volatile components.

[0188] The slurry forming unit is designed for mixing the purified solution containing the polyester depolymerization product with monomer B (HOOC-R2-COOH).

[0189] The slurry forming unit is preferably equipped with an inlet opening for the purified solution containing the polyester depolymerization product in liquid and an inlet for the individual monomer B (HOOC-R2-COOH) in solid form. Optionally diacid monomerB is supplied together with additional individual monomer A (HO-R1-OH) or also optionally a separate inlet opening for additional individual monomer A (HO-R1-OH) is provided. These openings are preferably located at the upper end of the unit.

[0190] The unit may be further equipped with an outlet opening for the slurry containing the polyester depolymerization product. This opening is preferably located at the lower end of the unit.

[0191] The unit may be further equipped with an outlet opening for substances which are in gaseous form at the conditions required to provide the purified solution containing the polyester depolymerization product in liquid form. This opening is preferably connected to condensing means which allow the recovery of evaporated liquids.

[0192] The unit may be further equipped with mixing and whipping means. Such mixing and whipping means may comprise blades or paddles on a rotating shaft or a single screw or parallel screws.

[0193] The unit may be further equipped with heating means. Such heating means may constitute mantle heating or heated element inside the unit. Heating means must be designed to provide sufficient heating to maintain the purified solution containing the polyester depolymerization product in liquid form, even when lower temperature monomer B and / or A is added.

[0194] The unit for the preparation of the slurry may be an addition to the design of a process to produce a polyester. In this case, the vessel becomes part of the device for the supply of a slurry containing the polyester depolymerization product.Alternatively, the unit may replace the vessel for the preparation of a monomer slurry predominantly made from individual monomer A (HO-R1-OH) and individual monomer B (HOOC-R2-COOH) of a conventional process to produce a polyester. In one preferred embodiment of the present invention, the existing vessel for the preparation of a monomer slurry predominantly made from individual monomer A and individual monomer B is used for the preparation of a slurry according to the present invention.

[0195] Whereas individual monomer A (HO-R1-OH) comprises the group of diols in unreacted form, monomer units A' (HO-R1-O-) and A' ’ (-0-R2-0-) comprise reacted diol units. Whereas individual monomer B (HOOC-R2-COOH) comprises the group of diacids in unreacted form, monomer units B' (HOOC-R2-CO- ) and B' ' (-OC-R2-CO-) comprise reacted diacid units.

[0196] A preferred embodiment of the present invention requires that monomer A (HO-R1-OH) comprises at least 90% of ethylene glycol (EG), wherein the percentage is calculated as mole percent of the total amount of individual monomer A, and monomer B (HOOC-R2-COOH) comprises at least 90% of terephthalic acid (TPA), wherein the percentage is calculated as mole percent of the total amount of individual monomer B.

[0197] Other suitable forms of monomers may comprise any comonomers typically used in manufacturing polyesters, like isophthalic acid (IPA), cyclohexanedimethanol (CHDM) or diethylene glycol (DEG).

[0198] The polyesters made from these monomers belong to the group of polyethylene terephthalates and their copolymers (PET) with a dominant repeat unit [TPA-EG-].When using PET with EG as individual monomer A for depolymerization, the main depolymerization product will be bis (hydroxyethyl ) terephthalate (BHET), and its dimers and oligomers. It is obvious that in the presence of comonomers, comonomer-substituted BHET, dimers and oligomers may be formed. For example, DEG may replace EG as reacted monomer A' or A' ’. Upon re-polymeriza-tion, again PET will be obtained. Based on the present invention the PET is formed by adding TPA.

[0199] In the depolymerization product from PET and EG the majority of depolymerization products are terminated by OH end groups, some COOH end groups will be present. The depolymerization product may also contain mono ( 2-hydroxyethyl ) -terephthalate (MHET) and TPA.

[0200] The same preferred ranges for depolymerization and for the slurry preparation and subsequent manufacturing of PET apply as defined above for the general polyesters.

[0201] In a preferred embodiment of the present invention the polyester after step c2 ) is a polyethylene terephthalate or one of its copolymers (PET), which has a molecular weight corresponding to an intrinsic viscosity of 0.75dl / g or higher, preferably 0.8dl / g or higher, more preferably 0.85dl / g or higher and most preferably 0.9dl / g or higher. The intrinsic viscosity ( TV) value indicates the intrinsic viscosity of a polymer and is a measure of its molecular weight. The IV value and its determination are known from the prior art.

[0202] Such PET is typically obtained from a PET after step cl ), having a molecular weight below an intended molecular weight, by increasing the molecular weight of the PET to the intended molecu-lar weight after step c2 ). Preferably the molecular weight increases after step cl ) corresponds to an intrinsic viscosity increase of 0.15dl / g or higher, more preferably 0.2dl / g or higher, most preferably 0.25dl / g or higher.

[0203] Polyesters according to the present invention can be used for a variety of applications, such as the production of short fibers and resulting yarns thereof, the production of packaging materials, especially films, sheets and containers and the production of filaments and resulting yarns thereof.

[0204] In a preferred embodiment of the present invention, the polyester is used for the preparation of a yarn, comprising the steps:

[0205] dl ) providing a polyester melt from a polyester prepared by the process described above,

[0206] d2 ) extruding the polyester melt through at least one die opening to obtain at least one polyester strand,

[0207] d3) cooling the at least one polyester strand to obtain a solid polyester filament,

[0208] d4 ) winding a single polyester filament or a multitude of polyester filaments to obtain a polyester mono-filament yarn or a polyester multi-filament yarn, and optionally

[0209] d5) drawing and stretching the polyester strand or polyester filament during or after step d3).

[0210] Providing the polyester melt in step dl ) may comprise melting, such as melting in an extruder, or directly providing a melt after melt phase polymerization. Such processes are known to the skilled person. Additives, such as colorants or inorganic fillers, may be added to the melt. Optionally the melt may be filtered.

[0211] Extruding the polyester melt through at least one die opening to obtain at least one polyester strand in step d2 ) may comprisethe use of single die with a single die opening, but typically involves dies with multiple openings (spinnerets). Such dies are known from the spinning industry. Preferably, said die with a single opening or multiple openings is provided at the outlet of an extruder, so that the extruded material leaves the extruder through said die.

[0212] Cooling the at least one polyester strand to obtain a solid polyester filament in step d3) may comprise any cooling fluid, which is applied to the strand (s) after leaving the die (s). Typically, air is used as cooling fluid. Alternatively, water or a water mist may be used.

[0213] Winding in step d4 ) may be performed by spools or bobbins. Winding a single polyester filament will provide a polyester monofilament yarn. Winding multitude polyester filaments will provide a polyester multi-filament yarn.

[0214] Optionally drawing, stretching, tempering, relaxing, texturing or twisting the polyester strand or polyester filament during or after step d3) may be performed to modify the properties of the yarn. Further other polymers or other polyesters may be used to create yarn blends or layered yarns. Spinning oils may be applied during any step of d3) or thereafter.

[0215] A yarn manufactured according to the present invention will always comprise a recycled polyester content.

[0216] Most preferred according to the present invention is a high tenacity monofilament or multi-filament yarn manufactured from polyethylene terephthalate or one of its copolymers (PET) with a molecular weight corresponding to an intrinsic viscosity of 0.85 or higher, preferably 0.9 or higher. Such high tenacity yarnsrequire a high degree of purity for consistent and uninterrupted spinning. Such purity is typically not obtainable by conventional recycling and requires almost complete removal of particles resulting from residues of liquifying contaminants or solid particles.

[0217] Such high tenacity yarns may be used to manufacture seat belts, airbags, tire cord, nets and ropes or geotextiles.

[0218] The rPET content in a yarn obtained by the present invention will be visible based on the content of suitable trace molecules which originate from post-industrial or post-consumer use of PET articles introduced into the process according to the present invention. Contrary to the present invention, yarns containing recycled monomers (i. e. not depolymerization products as in the present invention) will not show significant amounts of the trace molecules as they are removed as part of monomer production. At the same time, mechanically recycled PET will show the trace molecules but due to their lower molecular weight will not be suitable to produce yarns from high molecular weight PET.

[0219] Suitable trace molecules originating from post-industrial use may be part of the content in a container which has been directed to recycling before distribution to consumers. Suitable trace molecules originating from post-consumer use may be part of the content in a container which has been directed to recycling after distribution to consumers. Such suitable trace molecules may be part of the initial container content or part of the content introduced by the consumer (misuse by the consumer), for example to store household chemicals. Suitable trace molecules originating from post-industrial or post-consumer use may also be chemicals that are used in the preparation of the articles for further recycling, such as washing chemicals, surfactants, anti-foaming chemicals.Suitable trace molecules must not form from PET itself. For example, polymers of ethylene glycol may be present in cosmetic products but may also form from ethylene glycol during PET processing.

[0220] Suitable trace molecules must not result from typical additives used in yarn manufacturing, such as colorants or spinning oils.

[0221] Suitable trace molecules are fragrances such as limonene (CAS 138-86-3) typically resulting from food packaging or cosmetic packaging, or any forms of terpineol (such as a-terpineol CAS 98-55-5, p-terpineol CAS 138-87-4, y-terpineol CAS 586-81-2, 4-ter-pineol CAS 562-74-3) resulting from food or cosmetic packaging. Suitable trace molecules are solvents such as any forms of dipropylene glycol (such as CAS 106-62-7, 108-61-2, 110-98-5 and 25265-71-8 ), typically resulting from cosmetic packaging or wash chemicals.

[0222] The presence of rPET in the yarn obtained according to the present invention is characterized by a content of suitable trace molecules above 30ppb (microgram per kilogram), preferably above lOOppb, more preferably above 300ppb.

[0223] The content of trace molecules is measured either directly from the optionally ground polyester yarn, for example by head space GC / MS characterization and quantification. Alternatively, the polyester yarn may be extracted with a solvent and the characterization and quantification is obtained by GC analysis of the extract.

[0224] While during the use of a yarn suitable tracer molecules may be absorbed, the presence of rPET according to the present invention is indicated by the presence of suitable trace molecules inthe yarn in its original form, as obtained directly after the yarn manufacturing process.

[0225] The present invention is furthermore related to a device for carrying out the process according to the present invention, comprising

[0226] a reaction vessel for at least partial depolymerization of a polyester,

[0227] a mixing unit arranged downstream of the reaction vessel, wherein a first inlet of the mixing unit is fluidly connected to an outlet of the reaction vessel, and wherein said mixing unit further comprises a second inlet,

[0228] a first separating unit, preferably a filter, for removing solidified liquifying contaminant, said first separating unit being arranged downstream of the mixing unit, wherein an inlet of the first separating unit is fluidly connected to an outlet of the mixing unit,

[0229] characterized in that an outlet of said first separating unit is fluidly connected to the second inlet of the mixing unit, via a cooling unit arranged between the first separating unit and the mixing unit.

[0230] The units have already been discussed above.

[0231] In the reaction vessel, step a3) of the process of the present invention is carried out. Thus, a blend comprising the waste stream (W) and at least one diol monomer HO-R1-OH (A), which is capable of reacting with the polyester, is formed before or in the reaction vessel, and therein subj ected to conditions described above resulting in at least partial depolymerization of a polyester. The reaction vessel has at least one inlet, preferably at least two inlets, for inserting said blend comprising the waste stream (W) and at least one diol monomer HO-R1-OH (A),or for separately inserting the waste stream (W) and at least one diol monomer HO-R1-OH (A), wherein in said second variant the diol monomer HO-R1-OH (A) may be a part of the purified solution (PS) obtained in step a5) of the process of the present invention. The reaction vessel has at least one outlet, preferably one outlet, from which a depolymerization solution (DPS) containing the polyester depolymerization product that is generated in step a3) exits the reaction vessel.

[0232] A mixing unit is arranged downstream of the reaction vessel. The mixing unit and the reaction vessel are fluidly connected with each other, preferably with a line (such as a pipe) that connects the at least one outlet of the reaction vessel with one inlet of the mixing unit. A regulating component may be provided in order to regulate the flow of the depolymerization solution (DPS).

[0233] Said mixing unit comprises at least one additional inlet, preferably 1 to 2 additional inlets, for the insertion of the cooling liquid (C) and optionally diol monomer (A).

[0234] As discussed above, in said mixing unit mixing of the depolymerization solution (DPS) from step a3) with a cooling liquid (C) takes place, to obtain a diluted solution (DS) having a temperature T3 at which the liquifying contaminant is solidified. The mixing unit has at least one outlet, preferably one outlet, from which said diluted solution (DS) exits the mixing unit.

[0235] A first separating unit is arranged downstream of the mixing unit. The mixing unit and the first separating unit are fluidly connected with each other, preferably with a line (such as a pipe) that connects the at least one outlet of the mixing unitwith one inlet of the first separating unit. A regulating component may be provided in order to regulate the flow of the depolymerization solution (DS).

[0236] As discussed above, said first separating unit is preferably a filter or a density separation unit, such as a decanter or a simple sedimentation tank, for removing solidified liquifying contaminant, to obtain purified solution (PS). The first separating unit has at least one outlet from which said purified solution (PS) exits the first separating unit. A second outlet is typically provided for removing solidified liquifying contaminant.

[0237] It is an essential feature of the process of the present invention that the cooling liquid (C) that is added in step a4 ) is a portion of the purified solution (PS) containing polyester depolymerization product obtained in step a5) in said first separating unit. Thus, an outlet of said first separating unit is fluidly connected to the second inlet of the mixing unit (2 ), via a cooling unit arranged between the first separating unit and the mixing unit.

[0238] The mixing unit, the first separating unit and the cooling unit are fluidly connected with each other, preferably with lines (such as a pipe) that connects the at least one outlet of the first separating unit with one inlet of the cooling unit, and connects at least one outlet of the cooling unit with at least one inlet of the mixing unit. In said connecting lines, a regulating component such as a valve or a dosing pump may be provided in order to regulate flow of the depolymerization solution (PS).In said cooling unit, the purified solution (PS) is adjusted to the temperature T2 discussed above. Said cooling unit may be any conventional cooling unit, such as a plate or a pipe heat exchanger as the purified solution (PS) is now essentially free of liquifying contaminant and at a temperature at which the liquifying contaminant is in solid form and therefore has a low tendency to adhere to the surface of the heat exchanger.

[0239] In a preferred embodiment, said outlet of said first separating unit is additionally fluidly connected to an inlet of the reaction vessel, preferably with a line (such as a pipe). A regulating component may be provided in order to regulate the flow of the depolymerization solution (PS). In this embodiment, another portion of the purified solution (PS) containing the polyester depolymerization product obtained in step a5) can be added into step a2 ) and thus serve as a source for diol monomer A.

[0240] In another preferred embodiment, the device furthermore comprises a second separating unit, preferably a mechanical separation unit, for removing precipitated polyester depolymerization product, wherein said second separating unit is arranged downstream of the first separating unit and is fluidly connected, preferably with lines (such as a pipe), to the outlet of the first separating unit via the cooling unit arranged between the first separating unit and the second separating unit, so that the first separating unit is fluidly connected to the second inlet of the mixing unit, via the cooling unit and the second separating unit. A regulating component may be provided in order to regulate the flow of the depolymerization solution (PS).

[0241] With this embodiment, the above discussed variant of the process of the present invention can be carried out where the portion ofthe purified solution (PS) containing the polyester depolymerization product to be used as the cooling liquid (C) in step a4 ) is obtained by cooling the purified solution (PS) containing the polyester depolymerization product obtained in step a5) so as to precipitate polyester depolymerization product, and subsequently separating purified solution (PS), preferably by a mechanical separation, into a fraction rich in the polyester depolymerization product and a fraction rich in the diol monomer (A), wherein at least a part of the fraction rich in the diol monomer (A) is the portion to be used as the cooling liquid (C) in step a4 ).

[0242] Said mechanical separator may be a filter or preferably a density separator, such as a decanter, centrifuge, hydro cyclone or a simple sedimentation tank, but any other conventional mechanical separation unit may be used.

[0243] In another preferred embodiment, the device furthermore comprises a slurry forming unit, wherein said slurry forming unit has a first inlet for introducing a diacid monomer, and a second inlet that is fluidly connected to a component selected from the group consisting of the first separating unit and the second separating unit. Fluid connections are realized preferably with a line (such as a pipe) that connects the respective units with each other. A regulating component may be provided in order to regulate the flow of the respective medium.

[0244] The slurry forming unit has already been described above. In said unit, a slurry is formed which is the basis for a subsequent polymerization. Thus, an outlet of the slurry forming unit is preferably fluidly connected to a polymerization unit preferably with a line (such as a pipe). A regulating component may be provided in order to regulate the flow of the slurry.In another embodiment of the present invention, as discussed above the slurry may not be directly transferred into a polymerization unit. In said embodiment, the slurry forming unit is fluidly connected to the second inlet of the mixing unit, optionally via the cooling unit arranged between the first separating unit and the mixing unit. Fluid connections are realized preferably with lines (such as a pipe) that connects the respective units with each other. A regulating component may be provided in order to regulate flow of the depolymerization solution (PS). The advantage of this arrangement is that it allows providing the diacid component which is typically available at room temperature to the slurry preparation unit below the temperature T3 and therefore facilitates cooling to temperature T2 of the stream being directed to the mixing unit.

[0245] In another preferred embodiment, the device furthermore comprises a third separating unit, containing a screen or filter material, suitable to let a solution pass but retaining solid contaminants. Said third separating unit has a first inlet, that is fluidly connected to an outlet of the reaction vessel, and a first outlet that is fluidly connected to an inlet of the mixing unit. Alternatively, or in addition, the device may furthermore comprise a third separating unit, containing a screen or filter material, suitable to let a solution pass but retaining solid contaminants. Said third separating unit has a first inlet, that is fluidly connected to the first separating unit, and a first outlet that is fluidly connected to the slurry forming unit. In both cases said separating unit has at least a second outlet where solid contaminants, having a size larger than the opening in the screen of filter material can be removed, either in continuous mode or in batch mode, typically by emptying and / or cleaning the screen or filter material.In another preferred embodiment, the device furthermore comprises an adsorption unit, containing an adsorbent suitable to adsorb contaminants such as undesirable organic substances, especially colors or metal ions. Said adsorption unit has a first inlet, that is fluidly connected to an outlet of the first separating unit, and a first outlet that is fluidly connected to an inlet of the mixing unit.

[0246] Alternatively, or in addition, the device may furthermore comprise an adsorption unit, containing an adsorbent suitable to adsorb contaminants such as undesirable organic substances, especially colors or metal ions. Said adsorption unit has a first inlet, that is fluidly connected to a component selected from the group consisting of an outlet of the first separating unit and an outlet of the third separating unit positioned downstream of the first separating unit. Said adsorption unit has a first outlet that is fluidly connected to the slurry forming unit.

[0247] In both cases said adsorption unit has at least a second opening where adsorbent can be inserted and / or removed.

[0248] The units in the device according to the present invention are fluidly connected by connecting lines as described.

[0249] In said connecting lines, a regulating component such as a valve or dosing pump may be provided in order to regulate flow. However, flow and liquid transfer amounts may also be determined by other means, such as level control or weight control inside the units or between the units.

[0250] Additional pumping means and / or storage units may be provided between the different units of the device according to the present invention.Any of the units and transfer lines may comprise additional means such as mixing units, heating or cooling units, instruments and valves. Any unit, especially the reaction vessel may comprise at least one outlet opening to remove substances in gaseous form. Any unit, especially the first separating unit may comprise openings to provide cleaning liquids.

[0251] The present invention will be described below in more detail with reference to non-limiting examples and drawings.

[0252] Fig. l shows a first embodiment of a device according to the present invention for carrying out a first embodiment of the process of the present invention.

[0253] Fig. 2 shows a second embodiment of a device according to the present invention for carrying out a second embodiment of the process of the present invention.

[0254] Fig. 3 shows a third embodiment of a device according to the present invention for carrying out a third embodiment of the process of the present invention.

[0255] Fig. 4 shows a fourth embodiment of a device according to the present invention for carrying out a fourth embodiment of the process of the present invention.

[0256] Fig. 5 shows a fifth embodiment of a device according to the present invention for carrying out a fifth embodiment of the process of the present invention.

[0257] Fig. 6 shows an embodiment not according to the present invention where as compared to the embodiment of Fig. 1 no purified solution is returned as cooling unit.

[0258] Fig. 1 shows a first embodiment of a device D according to the present invention for carrying out a first embodiment of the process of the present invention.Said device D comprises a reaction vessel 1, in which step a3) of the process of the present invention is carried out. Thus, in this embodiment a blend comprising the waste stream (W) and at least one diol monomer HO-Rl-OH (A), which is capable of reacting with the polyester, is formed before the reaction vessel 1, and therein subj ected to conditions described above resulting in at least partial depolymerization of a polyester.

[0259] In this embodiment, the reaction vessel 1 has one inlet lai for inserting said blend comprising the waste stream (W) and at least one diol monomer HO-R1-OH (A). In this embodiment, the reaction vessel 1 has one outlet lb, from which a depolymerization solution (DPS) containing the polyester depolymerization product that is generated in step a3) exits the reaction vessel 1.

[0260] A mixing unit 2 is arranged downstream of the reaction vessel 1. The mixing unit 2 and the reaction vessel 1 are fluidly connected with each other, preferably with a line (such as a pipe) that connects the outlet lb of the reaction vessel 1 with one inlet 2al of the mixing unit 2. In said connecting line, a pumping and / or regulating component (not shown) may be provided in order to regulate flow of the depolymerization solution (DPS).

[0261] In this embodiment, the mixing unit 2 comprises one additional inlet 2a2 for the insertion of the cooling liquid (C).

[0262] In said mixing unit mixing of the depolymerization solution (DPS) from step a3) with a cooling liquid (C) takes place, to obtain a diluted solution (DS) having a temperature T3 at which the liquifying contaminant is solidified. In this embodiment, the mixing unit has one outlet 2b, from which said diluted solution (DS) exits the mixing unit.A first separating unit 3 is arranged downstream of the mixing unit 2. The mixing unit 2 and the first separating unit 3 are fluidly connected with each other, preferably with a line (such as a pipe) that connects the outlet 2b of the mixing unit 2 with one inlet 3a of the first separating unit 3. In said connecting line, a pumping and / or regulating component (not shown) may be provided in order to regulate flow of the depolymerization solution (DS ).

[0263] Said first separating unit 3 is preferably a filter, a density separation unit, such as a decanter or a simple sedimentation tank, for removing solidified liquifying contaminant, to obtain purified solution (PS). In this embodiment, the first separating unit 3 has one outlet 3b from which said purified solution (PS) exits the first separating unit 3. A second outlet (not shown) is typically provided for removing solidified liquifying contaminant from the first separating unit 3.

[0264] In this embodiment, the outlet 3b of said first separating unit 3 is fluidly connected to the second inlet 2a2 of the mixing unit 2, via a cooling unit 4 arranged between the first separating unit 3 and the mixing unit 2.

[0265] The mixing unit 2, the first separating unit 3 and the cooling unit 4 are fluidly connected with each other, preferably with lines (such as a pipe) that connects the outlet 3b of the first separating unit 3 with one inlet of the cooling unit 4, and connects one outlet of the cooling unit 4 with at least one inlet 2a2 of the mixing unit 2. In said connecting lines, a pumping and / or regulating component (not shown) may be provided in order to regulate flow of the depolymerization solution (PS).In this embodiment, the connecting line fluidly connecting the outlet 3b of said first separating unit 3 with one inlet of the cooling unit 4 has a branching line that fluidly connects the outlet 3b of said first separating unit 3 with an inlet 5a2 of a slurry forming unit 5. Through said connecting line, at least a portion of the purified solution PS may be transferred into the slurry forming unit 5. In said connecting line, a pumping and / or regulating component (not shown) may be provided in order to regulate flow of the purified solution PS.

[0266] The slurry forming unit 5 has a second inlet 5al for insertion of a diacid monomer B. In said slurry forming unit 5, a slurry S is formed which is the basis for a subsequent polymerization. In this embodiment, an outlet 5b of the slurry forming unit 5 is fluidly connected to a polymerization unit 6, preferably with a line (such as a pipe). In said connecting line, a pumping and / or regulating component (not shown) may be provided in order to regulate flow of the slurry S.

[0267] Fig. 2 shows a second embodiment of a device D according to the present invention for carrying out a second embodiment of the process of the present invention.

[0268] The device and embodiment of Fig. 2 differs from the device and embodiment of Fig. 1 in that the connecting line fluidly connecting the outlet 3b of said first separating unit 3 with one inlet of the cooling unit 4 has an additional branching line that fluidly connects the outlet 3b of said first separating unit 3 with an additional inlet la2 of the reactor vessel 1. Through said connecting line, at least a portion of the purified solution PS may be transferred into the reactor vessel 1. In said connecting line, a pumping and / or regulating component(not shown) may be provided in order to regulate flow of the purified solution PS.

[0269] In this embodiment, the mixing unit 2 has an additional inlet 2a3 for insertion of diol monomer A. Since in this embodiment diol monomer A is provided to the reactor vessel 1 as part of the purified solution PS, it may not be necessary to add fresh diol monomer A to step aS) of the process of the present invention. However, it may be necessary in certain variants to provide fresh diol monomer A into the mixing unit 2, to adjust the amount of diol monomer in the depolymerization solution (DPS), diluted solution (DS) and purified solution (PS).

[0270] It will be understood that any branching of a line may be substituted by an additional outlet from the previous process unit.

[0271] Fig. 3 shows a third embodiment of a device D according to the present invention for carrying out a third embodiment of the process of the present invention.

[0272] The device and embodiment of Fig. 3 differs from the device and embodiment of Fig. 1 in that a second separating unit 7 is provided. In said second separating unit 7, preferably a mechanical separation unit, precipitated polyester depolymerization product is removed. In this embodiment, said second separating unit 7 is arranged downstream of the first separating unit 3 and is fluidly connected, preferably with lines (such as a pipe), to the outlet 3b of the first separating unit 3 via the cooling unit 4 arranged between the first separating unit 3 and the second separating unit 7, so that the first separating unit 3 is fluidly connected to the second inlet 2a2 of the mixing unit 2, via the cooling unit 4 and the second separating unit 7. In said connecting lines, a pumping and / or regulating component (not shown)may be provided in order to regulate flow of the depolymerization solution (PS).

[0273] In this embodiment, the second separating unit 7 has an additional outlet which is fluidly connected with an inlet 5a2 of a slurry forming unit 5. Through said connecting line, at least a portion of the purified solution PS may be transferred into the slurry forming unit 5. In said connecting line, a pumping and / or regulating component (not shown) may be provided in order to regulate flow of the purified solution PS.

[0274] In this embodiment, the slurry forming unit 5 is not directly connected with the first separating unit 3.

[0275] Fig. 4 shows a fourth embodiment of a device D according to the present invention for carrying out a fourth embodiment of the process of the present invention.

[0276] The device and embodiment of Fig. 4 differ from the device and embodiment of Fig. 3 in that the slurry S formed in the slurry forming unit 5 is not directly transferred into the polymerization unit 6. In this embodiment, the outlet 5b of the slurry forming unit 5 is fluidly connected to the second inlet 2a2 of the mixing unit 2, so that slurry S comprising a portion of the purified solution PS is inserted as cooling liquid C into the mixing unit 2.

[0277] The mixing unit 2 and the slurry forming unit 5 are fluidly connected with each other, preferably with a line (such as a pipe). In said connecting line, a pumping and / or regulating component (not shown) may be provided in order to regulate flow of the slurry S.In this embodiment, the slurry S is transferred into the polymerization unit 6 from an outlet of the second separating unit 7, after having undergone one or more cycles through the mixing unit 2, the first separating unit 3, the cooling unit 4 and the second separating unit 7.

[0278] Fig. 5 shows a fifth embodiment of a device D according to the present invention for carrying out a fifth embodiment of the process of the present invention.

[0279] The device and embodiment of Fig. 5 differ from the device and embodiment of Fig. 4 in that no second separating unit 7 is provided. The slurry forming unit 5 is provided between the first separating unit 3 and the cooling unit 4, and is fluidly connected as in the other embodiments, preferably via lines (such as pipes) to the outlet 3b of the first separating unit 3 and an inlet of the cooling unit 4. In said connecting lines, a pumping and / or regulating component (not shown) may be provided in order to regulate flow of the slurry S.

[0280] In this embodiment, the outlet 5b of the slurry forming unit 5 is fluidly connected to the second inlet 2a2 of the mixing unit 2 via the cooling unit 4, so that slurry S comprising a portion of the purified solution PS is inserted as cooling liquid C into the mixing unit 2.

[0281] In this embodiment, the slurry S is transferred into the polymerization unit 6 from the outlet 3b of the first separating unit 3, after having undergone one or more cycles through the cooling unit 4, the mixing unit 2, and the first separating unit 3.In an alternative to Figures 1, 3, 4 and 5, the reaction vessel 1 may have one additional inlet la3 (not shown) for feeding at least one diol monomer HO-R1-OH (A).

[0282] The units in the device D according to the present invention are fluidly connected by connecting lines as described.

[0283] In said connecting lines, a regulating component, such as a valve or dosing pump, may be provided in order to regulate flow. Alternatively, flow regulation may be achieved by combining a pumping unit and measurement unit, such as a flow meter, a level sensor, a weight sensor or a temperature sensor. These sensors may be installed so that they connect to the connecting lines and / so that they connect to the units 1-7 and / or any additionally installed unit.

[0284] Additional pumping units and / or storage units may be provided between the different units 1-7 of the device D according to the present invention.

[0285] Fig. 6 shows an embodiment not according to the present invention where as compared to the embodiment of Fig. 1 no purified solution is returned as cooling unit. A portion of the diol monomer A is supplied to the mixing unit 2 as cooling liquid C instead. Excess diol monomer A is removed by precipitating and filtering the polyester depolymerization product and subsequent drying thereof.

[0286] In this embodiment, the purified solution (PS) is led from the first separating unit 3 to the cooling unit 4 and cooled therein. However, the cooled purified solution is not led to the mixing unit 2, but transferred into a fourth separating unit 8 for separating diol monomer A that was added before as residualdiol monomer A from depolymerization and cooling liquid C. In said fourth separating unit 8, diol monomer A such as EG is removed from the purified solution by conventionally known methods, for example by crystallization, optionally using at least one anti-solvent, and filtration of the depolymerization product, optionally using washing liquids, and / or by distillation from the purified solution, the filtrate and / or the depolymerization product after filtration. The separating unit 8 may comprise multiple individua units for different separation steps.

[0287] The depolymerization product separated from excess diol monomer A is then led into the slurry forming unit 5, as described above for the embodiment of Fig. 1.Example 1

[0288] The method of the present invention was carried out according to the embodiment of Fig. 1.

[0289] The following flow rates according to Fig. 1 were used:

[0290] W = 1000kg / h PET + 50kg / h polyethylene (PE) (PET flakes derived from used PET trays having a polyethylene copolymer-based sealant layer (PE), said PE having a DSC melting point of 113°C, a stickiness temperature range of 100 to 115°C and showing strong stickiness above 115°C)

[0291] A = EG = 1614kg / h; molar ratio EG: PET repeat units = 5: 1

[0292] B = TPA = 3323kg / h; molar ratio according to A: B = 1.3: 1 C: DPS weight ratio = 1. 6: 1

[0293] PE: DS after separation = 1: 1

[0294] The PET flakes were depolymerized in a reaction vessel 1 with ethylene glycol (EG) under reflux for 4 hours, to obtain 2664 kg / h depolymerization solution DPS. The resulting depolymerization solution DPS was transferred to a mixing unit 2 at a temperature T1 of 180°C and was mixed in a mixing unit 2 with 4262 kg / h of cooling solution C having a temperature T2 of 40°C. Said cooling solution C was a portion of the subsequently obtained purified solution PS and contained 44 wt. -% polyester depolymerization product.

[0295] 6926 kg / h of diluted solution DS were obtained. Said DS had a temperature T3 of 98 °C, at which temperature agglomerated PE particles (the liquifying contaminant) had solidified and 50kg of PE together with about 50kg solution was removed by filtration in a first separating unit 3, so as to obtain 6826kg / h purified solution PS. A portion of said purified solution PS wasused as cooling solution C, as described above, after being cooled in a cooling unit 4 to a temperature T2 of 40°C.

[0296] The purified solution PS was transferred into a slurry forming unit 5, where the TPA was added and 5887 kg / h of a slurry S with total A units: total B units = 1.22: 1 was formed. Said slurry S was transferred into a polymerization unit 6.

[0297] During polymerization, about 342kg / h EG had to be evaporated as a result of the applied molar ratio A: B, which represents 1.06 mol per mol repeat units of PET in W.

[0298] After polymerization, 4827kg / h PET were obtained which contain 21% recycled PET.

[0299] The example shows a T3 below the stickiness temperature range of the liquifying contaminant without the need to add additional EG as a cooling liquid. Due to the significantly reduced addition of EG into the process, the added EG can be used in the repolymerization of the polyester.

[0300] Example 2

[0301] The method of the present invention was carried out according to the embodiment of Fig. 3.

[0302] The following flow rates according to Fig. 3 were used:

[0303] W = 1000kg / h PET + 50kg / h polyethylene (PE) (as described in example 1)

[0304] A = EG = 1614kg / h; molar ratio EG: PET repeat units = 5: 1

[0305] B = TPA = 3323kg / h; molar ratio according to A: B =1.3: 1

[0306] C: DPS weight ratio = 1.3: 1PE: DS after separation = 1: 1

[0307] The PET flakes were depolymerized in a reaction vessel 1 with ethylene glycol (EG) under reflux for 4 hours, to obtain 2664 kg / h depolymerization solution DPS. The resulting depolymerization solution DPS was transferred to a mixing unit 2 at a temperature T1 of 180°C and was mixed in a mixing unit 2 with 3463 kg / h of cooling solution C having a temperature T2 of 40°C. Said cooling solution C was a portion of the subsequently obtained purified solution PS and obtained as described below.

[0308] 6127 kg / h of diluted solution DS were obtained. Said DS had a temperature T3 of 99°C, at which temperature agglomerated PE particles (the liquifying contaminant) had solidified and 50kg of PE together with about 50kg so solution was removed by filtration in a first separating unit 3, so as to obtain 6027 kg / h purified solution PS.

[0309] A portion of said purified solution PS was used as cooling solution C, as described above, after being cooled in a cooling unit 4 to a temperature T2 of 40°C and being led through a second separation unit 7. In said second separation unit 7, the purified solution PS was separated into two portions. The first portion was transferred as cooling solution C to the mixing unit 2 and contained dimer in a ratio of 1: 4 with respect to the amount of dimer in the portion of the purified solution that was led to the slurry forming unit 5. As a result, the content of polyester depolymerization product in cooling liquid C was reduced to 8 wt-%.

[0310] The purified solution PS was transferred into a slurry forming unit 5, where the TPA was added and 5887 kg / h of a slurry S with total A units: total B units = 1.3: 1 was formed. Said slurry Swas transferred into a polymerization unit 6 and polymerized as described in example 1.

[0311] During polymerization, about 333kg / h EG had to be evaporated as a result of the applied molar ratio A: B, which represents 1.03 mol per mol repeat units of PET in W.

[0312] After polymerization, 4836kg / h PET were obtained which contain 21% recycled PET.

[0313] The example shows a T3 below the stickiness temperature of the liquifying contaminant without the need to add additional EG as a cooling liquid. Due to the significantly reduced addition of EG into the process, the added EG can be used in the re-polymerization of the polyester. The low solid content in the cooling liquid facilitates any adsorption processes as the liquid viscosity is lowered.

[0314] Comparative example 1

[0315] For comparison purposes (not according to the present invention), a method according to Fig. 6 was carried out. Said method differs from the embodiment according to Fig. 1 in that no transfer of cooling liquid C from the first separating unit 3 into the mixing unit 2 was carried out. Instead, fresh EG was supplied to the mixing unit 2 as cooling liquid.

[0316] The following flow rates according to Fig. 6 were used:

[0317] W = 1000kg / h PET + 50kg / h polyethylene (PE) (as described in example 1)

[0318] A = EG = 1614kg / h; mol ratio EG: PET repeat units = 5: 1

[0319] C = Fresh EG as cooling liquid with C: DPS ratio = 1.3: 1

[0320] B = TPA = 312kg / hPE: DS after separation = 1: 1

[0321] The PET flakes were depolymerized in a reaction vessel 1 with ethylene glycol (EG) with a molar ratio EG: PET repeat units = 5: 1 under reflux for 4 hours, to obtain 2664 kg / h depolymerization solution DPS. The resulting depolymerization solution DPS was transferred to a mixing unit 2 at a temperature T1 of 180°C and was mixed in a mixing unit 2 with 3463 kg / h of cooling solution C ( fresh EG) having a temperature T2 of 40°C. Said cooling solution C was fresh EG.

[0322] 6126 kg / h of diluted solution DS were obtained. Said DS had a temperature T3 of 98 °C, at which temperature agglomerated PE particles (the liquifying contaminant) had solidified and 50kg of PE together with about 50kg so solution and was removed by filtration in a first separating unit 3, so as to obtain 6026 kg / h purified solution PS.

[0323] The polyester depolymerization product was separated from the purified solution PS by dilution with an anti-solvent, cooling, crystallization and washing to obtain 1152kg / h polyester depolymerization product. To recover the EG as pure EG, 4875 kg / h of EG had to be evaporated, which represents 15 mol per mol repeat units of PET in W.

[0324] The resulting purified solution PS (separated from EG) was transferred into a slurry forming unit 5, where the TPA was added and 1464 kg / h of a slurry S with total A units: total B units = 1.1: 1 was formed. Said slurry S was transferred into a polymerization unit 6 and polymerized as described in example 1.

[0325] After polymerization, 1353kg / h PET were obtained which contain 74% recycled PET.While a high rPET content in the final PET was obtained, energy consumption for heating and cooling to prepare the depolymerization product that is transferred to re-polymerization was high. For the process it is required to separate the EG from the depolymerization product. Such a separation requires the use of antisolvents and washing liquids which again have to be separated from the EG before the EG can be reused.

Claims

Claims1. A process for the preparation of a purified solution (PS) containing a polyester depolymerization product, said polyester depolymerization product having a repeat unit [-A' ' -B' ' ] with the formula [ -O-R1-OOC-R2-CO- ] and having 1 to 9 repeat units, whereinR1and R2are the same or different and are selected from the group consisting of aliphatic hydrocarbons containing 1 to 15 carbon atoms, aromatic hydrocarbons containing 1 to 3 aromatic rings, cyclic hydrocarbons containing 4 to 10 carbon atoms, and heterocyclic rings containing 1 to 3 oxygen atoms and 3 to 10 carbon atoms,said method comprising the steps:al ) providing a waste stream (W) comprisinga polyester with the repeat unit [-A' ' -B' ' ] having the formula [ -O-R1-OOC-R2-CO- ], with more than 9 repeat units; anda liquifying contaminant at a concentration of 0.001 to 48% by weight, based on the entire amount of the waste stream, wherein the liquifying contaminant is defined as substances which are solid at room temperature but liquid and not soluble in the depolymerization solution formed in step a3) under the conditions of step a3), a2 ) forming a blend comprising the waste stream (W) and at least one diol monomer HO-R2-OH (A), which is capable of reacting with the polyester,a3) exposing the blend obtained in step a2 ) in a reaction vessel ( 1 ) to conditions suitable for at least partial depolymerization of the polyester resulting in a depolymerization solution (DPS) containing the polyester depolymerization product,a4 ) mixing the depolymerization solution from step a3), said depolymerization solution having a temperature Tl, with a cooling liquid (C) having a temperature T2, wherein T2< T1, to obtain a diluted solution (DS) having a temperature T3 at which the liquifying contaminant is solidified, wherein T2< T3< T1, anda5) removing solidified liquifying contaminant in solid form from the diluted solution (DS), so as to obtain the purified solution (PS) containing the polyester depolymerization product,characterized in that the cooling liquid (C) added in step a4 ) is a portion of the purified solution (PS) containing the polyester depolymerization product obtained in step a5) that has been adjusted to the temperature T2.

2. The process according to claim 1, characterized in that before being added into step a4 ), the cooling liquid is brought into contact with an absorption material.

3. The process according to claim 1 or 2, characterized in that the portion of the purified solution (PS) containing the polyester depolymerization product to be used as the cooling liquid (C) in step a4 ) is obtained by cooling the purified solution (PS) containing the polyester depolymerization product obtained in step a5) so as to precipitate the polyester depolymerization product, and subsequently separating the purified solution (PS), preferably by a mechanical separation, into a fraction rich in the polyester depolymerization product and a fraction rich in the diol monomer (A), wherein at least a part of the fraction rich in the diol monomer (A) is the portion to be used as the cooling liquid (C) in step a4 ).

4. The process according to claim 3, characterized in that after separation the fraction rich in the diol monomer (A) to beused as the cooling liquid (C) in step a4 ) has a temperature T4, wherein T4 = T2 ± 20°C, preferably T4 = T2 ± 10°C.

5. The process according to any one of the claims 1 to 4, characterized in that another portion of the purified solution (PS) containing the polyester depolymerization product obtained in step a5) is added into step a2 ).

6. The process according to any one of the claims 1 to 5, characterized in that between steps a3) and a4 ) a purification step is carried out to remove solid contaminants that are derived from the waste stream (W), said purification step preferably being a filtration, more preferably a filtration using a filter with a screen opening size of less than 20µm, more preferably less than 10µm.

7. The process according to any one of the claims 1 to 6, characterized in that between steps a3) and a4 ) the depolymerization solution (DPS) containing the polyester depolymerization product is cooled from a temperature T5 to the temperature Tl, wherein T1 +50°C ≥ T5 ≥ T1, preferably T1 +30°C ≥ T5 ≥ T1.

8. A process for the preparation of a polyester with a repeat unit [-A' ' -B' ' ] having the formula [ -O-R1-OOC-R2-CO- ], comprising the steps:a) providing a purified solution (PS) containing a polyester depolymerization product by the process according to any one of the claims 1 to 7,b) adding at least one diacid monomer (B) having the formula HOOC-R2-COOH to the purified solution of step a), to obtain a slurry ( S ), andc) using the slurry (S) from step b) for the polymerization of a polyester with the repeat unit [-A' ' -B' ' ] having the formula [ -O-R1-OOC-R2-CO- ],wherein R1and R2are the same or different and are selected from the group consisting of aliphatic hydrocarbons containing 1 to 15 carbon atoms, aromatic hydrocarbons containing 1 to 3 aromatic rings, cyclic hydrocarbons containing 4 to 10 carbon atoms, and heterocyclic rings containing 1 to 3 oxygen atoms and 3 to 10 carbon atoms.

9. The process according to claim 8, characterized in that between steps b) and c), the slurry (S) is reintroduced into step a4 ) of claim 1, as the cooling liquid (C).

10. The process according to claim 8 or 9, characterized in that in step c)cl ) the slurry (S) is polymerized by melt phase polymerization to obtain a polyester polymer having a molecular weight below an intended molecular weight, andc2 ) subsequently said polyester polymer is treated in the presence of a process gas at a temperature below its crystalline melting point to promote esterification and / or transesterification reactions, thereby increasing the molecular weight of the polyester.

11. The process according to claim 10, characterized in that side products from the esterification and / or transesterification reactions are transferred into the process gas, and said process gas is subsequently purified in a purification step using a liquid adsorption media, and the purified process gas is reentered into step c2 ), and the liquid adsorption media comprises a diol monomer which is reintroduced into step a4 ) of claim 1.

12. The process according to claim 10, characterized in that the polyester after step c2 ) is a polyethylene terephthalate orone of its copolymers, which has a molecular weight corresponding to an intrinsic viscosity of 0.75dl / g or higher.

13. A device ( D) for carrying out the process according to any one of claims 1 to 12, comprisinga reaction vessel ( 1 ) for at least partial depolymeri zation of a polyester,a mixing unit ( 2 ) arranged downstream of the reaction vessel ( 1 ), wherein a first inlet ( 2al ) of the mixing unit ( 2 ) is fluidly connected to an outlet ( lb ) of the reaction vessel ( 1 ), and wherein said mixing unit ( 2 ) further comprises a second inlet ( 2a2 ),a first separating unit ( 3 ), preferably a filter, for removing solidi fied liqui fying contaminant, said first separating unit ( 3 ) being arranged downstream of the mixing unit ( 2 ), wherein an inlet ( 3a ) of the first separating unit ( 3 ) is fluidly connected to an outlet ( 2b ) of the mixing unit ( 2 ), characteri zed in that an outlet ( 3b ) of said first separating unit ( 3 ) is fluidly connected to the second inlet ( 2a2 ) of the mixing unit ( 2 ), via a cooling unit ( 4 ) arranged between the first separating unit ( 3 ) and the mixing unit ( 2 ), and the device furthermore comprises a second separating unit ( 7 ), preferably a mechanical separation unit, for removing precipitated polyester depolymeri zation product, wherein said second separating unit ( 7 ) is arranged downstream of the first separating unit ( 3 ) and is fluidly connected to the outlet ( 3b ) of the first separating unit ( 3 ) via the cooling unit ( 4 ) arranged between the first separating unit ( 3 ) and the second separating unit ( 7 ), so that the first separating unit ( 3 ) is fluidly connected to the second inlet ( 2a2 ) of the mixing unit ( 2 ), via the cooling unit ( 4 ) and the second separating unit ( 7 ).

14. The device according to claim 13, characterized in that said outlet (3b) of said first separating unit (3) is additionally fluidly connected to an inlet ( la2 ) of the reaction vessel ( 1 ) •15. The device according to any one of claims 13 to 14, characterized in that the device (D) furthermore comprises a slurry forming unit (5), wherein said slurry forming unit (5) has a first inlet (5al ) for introducing a diacid monomer (B), and a second inlet (5a2 ) that is fluidly connected to a component selected from the group consisting of the first separating unit (3) and the second separating unit (7 ).

16. The device according to claim 15, characterized in that an outlet of the slurry forming unit (5) is fluidly connected to a polymerization unit ( 6).

17. The device according to claim 15, characterized in that an outlet of the slurry forming unit (5) is fluidly connected to the second inlet (2a2 ) of the mixing unit (2 ), preferably via the cooling unit (4 ) arranged between the first separating unit (3) and the mixing unit (2 ).

18. A process for the preparation of a yarn, comprising the steps:dl ) providing a polyester melt from a polyester prepared by the process according to claim 12,d2 ) extruding the polyester melt through at least one die opening to obtain at least one polyester strand, d3) cooling the polyester strand to obtain a solid polyester filament,d4 ) winding a single polyester filament or a multitude of polyester filaments to obtain a polyester mono-filament yarn or a polyester multi-filament yarn.

19. A high tenacity monofilament or multi-filament yarn composed of polyethylene terephthalate or one of its copolymers (PET), obtainable from a process according to claim 12 with a molecular weight corresponding to an intrinsic viscosity of 0.85 or higher, characterized in that the yarn contains 30ppb or more of a trace molecule indicating the presence of a recycled polyethylene terephthalate polyester.

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