Antifouling agents for plastic-derived synthetic materials

Abstract

Antifouling agents for use in compositions and methods for reducing or preventing contaminants in synthetic materials derived from plastics are disclosed. A method for reducing or preventing contamination in a plastic-derived synthetic feedstock composition may include adding a stain inhibitor comprising a copolymer of a carboxylic acid anhydride or dicarboxylic acid anhydride and an alpha-olefin to a synthetic feedstock composition derived from plastic pyrolysis containing contaminants to provide a treated pyrolysis product. The contaminants may include, for example, nylon, polyvinyl chloride, polyethylene terephthalate, polyamide, caprolactam, benzoic acid, phenol, p-cresol, dimethylphenol, isopropylphenol, tert-butylphenol, dimethylethylphenol, naphthalenol, alkenes and alkanes of various lengths, propylene, toluene, pentene, butane, tetramethylindole, ethylbenzene, ethyldimethylpyrrole, dimethylfuran, tetrahydroquinoline, and any combination thereof.

Description

[Technical field]

[0001] This application is directed to antifouling agents used in the production of synthetic materials derived from plastics. [Background technology]

[0002] Post-consumer and off-spec plastic materials can be chemically recycled by heating them in a pyrolysis reactor to break down the polymer chains into smaller volatile fragments. Vapors from the reactor are condensed and recovered as pyrolysis products or pyrolysis oil, while smaller non-condensable hydrocarbon fragments are recovered as fuel gas.

[0003] During recovery of pyrolysis products, contaminants such as black or brown residues or tarry materials that are insoluble in the pyrolysis oil accumulate and foul process equipment such as distillation columns, pumps, process piping, filters, etc. The buildup of contaminants that accumulate over time eventually necessitates the shutdown of equipment for cleaning.

[0004] When pyrolysis products (pyrolysis oil) are stored for long periods of time, the storage containers may also accumulate contaminants in the form of a film. This brownish-black film forms with or without the presence of air (oxygen). The film may form at room temperature over longer periods (e.g., one week), but film formation is accelerated at elevated temperatures. Summary of the Invention

[0005] DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS Compositions and methods for dispersing contaminants from pyrolysis oils derived from plastics are described herein.

[0006] One aspect of the present application is a method for reducing or preventing contamination in a plastic-derived synthetic feedstock composition, comprising: The method includes adding an antifouling agent comprising a copolymer of a carboxylic acid anhydride or dicarboxylic acid anhydride and an alpha olefin to a synthetic feedstock composition derived from plastic pyrolysis containing contaminants to provide a treated pyrolysis product.

[0007] In another aspect, a composition comprising a synthetic material derived from plastic, the synthetic material comprising: (a) heating the plastic at a temperature between about 400° C. and about 850° C. under substantially oxygen-free conditions to produce a pyrolysis effluent; (b) cooling and condensing the pyrolysis effluent to obtain synthetic feedstock; (c) recovering the synthetic raw materials; and (d) adding a soil release agent to the synthetic stock composition to provide a treated synthetic stock; (e) separating the treated synthetic feedstock to obtain a synthetic feedstock having reduced contaminants.

[0008] Yet another aspect is a treated synthetic pyrolysis product that includes synthetic feedstocks and contaminants and an antifouling agent, the antifouling agent being a copolymer that includes a carboxylic acid anhydride or dicarboxylic acid anhydride and an alpha olefin. [Brief description of the drawings]

[0009] [Figure 1] FIG. 1 is a schematic diagram of an embodiment of a plastic pyrolysis process.

[0010] [Diagram 2] FIG. 1 is a schematic diagram of an embodiment of a plastic pyrolysis process.

[0011] [Diagram 3] FIG. 1 is a schematic diagram of an embodiment of a plastic pyrolysis process showing treatment with an antifouling agent.

[0012] [Figure 4A-1] 1 shows infrared spectra of samples containing different contaminants. [Figure 4A-2] 1 shows infrared spectra of samples containing different contaminants. [Figure 4B] 1 shows infrared spectra of samples containing different contaminants.

[0013] [Diagram 5] 1 is a bar graph of desorption products of various membranes obtained after storage at various temperatures. Membrane contaminant samples are designated as follows: NE00632=blank pyrolysate without nitrogen at 25° C., NE00633=blank pyrolysate with nitrogen at 25° C., NE00634=blank without nitrogen at 43° C., NE00635=blank with nitrogen at 43° C., NE00636=blank pyrolysate without nitrogen at 75° C., NE00637=blank with nitrogen at 75° C.

[0014] [Figure 6] 1 is a digital photograph showing the effect of antifouling embodiments on film or residue formation after a 30 day stability test: low=200 ppm and high=1000 ppm. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0015] Although the present disclosure provides reference to various embodiments, those skilled in the art will recognize that changes may be made in form and detail without departing from the spirit and scope of the present application. Various embodiments are described in detail with reference to the drawings. Reference to various embodiments is not intended to limit the scope of the claims appended hereto. Additionally, any examples described in this application are not intended to be limiting, but merely to describe some of the many possible embodiments of the appended claims.

[0016] Unless otherwise defined, all technical and scientific terms used herein have the same meaning as commonly understood by those skilled in the art. In case of conflict, the present document, including definitions, shall prevail. Although methods and materials similar or equivalent to those described herein may be used in the practice or testing of this application, the methods and materials are described below. All publications, patent applications, patents, and other references mentioned herein are incorporated by reference in their entirety.

[0017] As used herein, the term "contaminants" refers to organic and inorganic materials that deposit on equipment during the handling and production of synthetic feedstocks or accumulate during storage (e.g., after processing of synthetic feedstocks).

[0018] As used herein, the term "process equipment" means distillation columns, pumps, process piping, filters, condensers, quench towers or columns, storage equipment, etc. that are associated with a process and may be subject to contamination. The term also includes a set of components that are in fluid or gas communication.

[0019] As used herein, the term "synthetic feedstock" refers to hydrocarbons (e.g., pyrolysis oils or pyrolysis products) obtained from treatments or processes on plastics, such as the thermochemical conversion of plastics.

[0020] As used herein, the term "optional" or "optionally" means that the subsequently described event or circumstance may occur, but need not occur, and that the description includes instances in which the event or circumstance occurs and instances in which the event or circumstance does not occur.

[0021] As used herein, any recited range of values ​​should be construed as supporting a claim reciting any subrange having endpoints that are real values ​​within the recited range, contemplating all values ​​within the range. As an example, disclosure herein of a range of 1-5 shall be deemed to support a claim to any of the following ranges: 1-5, 1-4, 1-3, 1-2, 2-5, 2-4, 2-3, 3-5, 3-4, and 4-5.

[0022] The terms "polymer," "copolymer," "polymerize," "copolymerize," and the like, include not only polymers that contain two monomer residues and polymerize two different monomers together, but also (co)polymers that contain more than two monomer residues and polymerize more than two or more other monomers together. For example, polymers disclosed herein include terpolymers, tetrapolymers, polymers that contain more than four different monomers, and polymers that comprise, consist of, or consist essentially of two different monomer residues. In addition, "polymers" disclosed herein can also include homopolymers, which are polymers that contain a single type of monomer unit.

[0023] Unless otherwise indicated, an "alkyl" group described herein alone or as part of another group is an optionally substituted linear or branched saturated monovalent hydrocarbon substituent containing from 1 to about 60 carbon atoms, such as from 1 to about 30 carbon atoms in the principal chain. Examples of unsubstituted alkyl groups include methyl, ethyl, n-propyl, i-propyl, n-butyl, i-butyl, s-butyl, t-butyl, n-pentyl, i-pentyl, s-pentyl, t-pentyl, and the like.

[0024] The term "aryl" or "ar" as used herein alone or as part of another group (e.g., arylene) refers to an optionally substituted homocyclic aromatic group, such as a monocyclic or bicyclic group containing about 6 to about 12 carbons in the ring portion, such as phenyl, biphenyl, naphthyl, substituted phenyl, substituted biphenyl, or substituted naphthyl. The term "aryl" also includes heteroaryl functional groups. It is understood that the term "aryl" applies to cyclic substituents that are planar and contain 4n+2n electrons according to Huckel's rule.

[0025] "Cycloalkyl" refers to a cyclic alkyl substituent containing, for example, about 3 to about 8 carbon atoms, preferably about 4 to about 7 carbon atoms, and more preferably about 4 to about 6 carbon atoms. Examples of such substituents include cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, and the like. Cyclic alkyl groups can be unsubstituted or can be further substituted with alkyl groups, such as methyl groups, ethyl groups, and the like.

[0026] "Heteroaryl" refers to a monocyclic or bicyclic 5- or 6-membered ring system, where the heteroaryl group is unsaturated and satisfies Hückel's rule. Non-limiting examples of heteroaryl groups include furanyl, thiophenyl, pyrrolyl, pyrazolyl, imidazolyl, 1,2,3-triazolyl, 1,2,4-triazolyl, isoxazolyl, oxazolyl, isothiazolyl, thiazolyl, 1,3,4-oxadiazol-2-yl, 1,2,4-oxadiazol-2-yl, 5-methyl-1,3,4-oxadiazole, 3-methyl-1,2,4-oxadiazole, pyridinyl, pyrimidinyl, pyrazinyl, triazinyl, benzofuranyl, benzothiophenyl, indolyl, quinolinyl, isoquinolinyl, benzimidazolyl, benzoxazolinyl, benzothiazolinyl, quinazolinyl, and the like.

[0027] The compounds of the present disclosure may be substituted with suitable substituents. The term "suitable substituents" as used herein is intended to mean a chemically acceptable functional group, preferably a moiety that does not negate the activity of the compound. Such suitable substituents include, but are not limited to, halo groups, perfluoroalkyl groups, perfluoroalkoxy groups, alkyl groups, alkenyl groups, alkynyl groups, hydroxy groups, oxo groups, mercapto groups, alkylthio groups, alkoxy groups, aryl or heteroaryl groups, aryloxy or heteroaryloxy groups, aralkyl or heteroaralkyl groups, aralkoxy or heteroaralkoxy groups, HO-(C=O)- groups, heterocyclic groups, cycloalkyl groups, amino groups, alkyl and dialkylamino groups, carbamoyl groups, alkylcarbonyl groups, alkoxycarbonyl groups, alkylaminocarbonyl groups, dialkylaminocarbonyl groups, arylcarbonyl groups, aryloxycarbonyl groups, alkylsulfonyl groups, and arylsulfonyl groups. In some embodiments, suitable substituents include halogen, unsubstituted C 1 ~C 12 Alkyl groups, unsubstituted C 4 ~C 6 Aryl group or unsubstituted C 1 ~C 10 Those skilled in the art will recognize that many of the substituents may be substituted with additional substituents.

[0028] The term "substituted" as in "substituted alkyl" means that in the group (i.e., the alkyl group), at least one hydrogen atom bonded to a carbon atom is substituted with a hydroxy (-OH), alkylthio, phosphino, amido (-CON(R A )(R B )(wherein, R A and R B are independently hydrogen, alkyl, or aryl), amino (-N(R A )(R B )(wherein, R A and R Bare independently hydrogen, alkyl, or aryl), halo (fluoro, chloro, bromo, or iodo), silyl, nitro (-NO 2 ), Ether (-OR A (In the formula, R A is alkyl or aryl), esters (-OC(O)R A (In the formula, R A is alkyl or aryl), keto (-C(O)R A (In the formula, R A means substituted with one or more substituents, such as alkyl or aryl, heterocyclo, etc.

[0029] Where the term "substituted" introduces a list of possible substituents, it is intended that the term apply to all members of that group, i.e., the phrase "optionally substituted alkyl or aryl" should be interpreted as "optionally substituted alkyl or optionally substituted aryl."

[0030] Compositions and methods are described that reduce or eliminate contaminants in synthetic feedstocks derived from plastics. Some contaminants in synthetic feedstock processes do not pyrolyze or volatilize at temperatures as high as 600°C. Treating such synthetic feedstocks with the antifouling agents described herein has been found to reduce or eliminate the contaminants. Such treated synthetic feedstocks exhibit reduced contamination of equipment and systems used in plastic recycling and during storage.

[0031] To recycle plastics, various plastic types, such as thermoplastic waste, can be used. Types of plastics commonly encountered in waste plastic feedstocks include, but are not limited to, low density polyethylene, high density polyethylene, polypropylene, polystyrene, and the like, and combinations thereof. In some embodiments, the synthetic feedstock comprises pyrolysis of plastics including polyethylene, polypropylene, polystyrene, polyethylene terephthalate, and combinations thereof. In some embodiments, polyethylene, polypropylene, and lesser amounts of polystyrene are present, while polyvinyl chloride and polyethylene terephthalate are present due to the difficulty of classification.

[0032] Several processes are known for converting plastics (e.g., waste plastics) into lower molecular weight hydrocarbon materials, particularly hydrocarbon fuel materials. See, for example, U.S. Patent Nos. 6,150,577, 9,200,207, and 9,624,439. Each of these publications is incorporated herein by reference in its entirety. Such processes, which have been broadly described, involve breaking down long-chain plastic polymers by thermochemical conversion, such as pyrolysis-pyrolysis (e.g., about 400°C to about 850°C), with limited or no oxygen and above atmospheric pressure. Pyrolysis temperatures can be reduced when catalysts are used. Pyrolysis conditions include temperatures of about 400°C to 850°C, about 500°C to 700°C, or about 600°C to 700°C. The resulting pyrolysis effluent is condensed and then optionally distilled.

[0033] As shown in FIG. 1, an embodiment of the pyrolysis process includes a waste plastic feeder 12, a reactor 14, and a condenser system 18. Polymer-containing material is fed through an inlet 10 in the feeder, and heat is added to the reactor 14. An outlet 20 from the condenser system 18 allows the product to exit. FIG. 2 depicts another embodiment of the pyrolysis process of plastics. FIG. 3 depicts yet another embodiment showing the process after condensation or quenching of the pyrolysis effluent. Thermal cracking reactors for achieving this pyrolysis reaction are described in detail in several patents, such as U.S. Pat. Nos. 9,624,439, 10,131,847, 10,208,253, and WO 2013 / 123377 A1, each of which is incorporated herein by reference in its entirety.

[0034] In some embodiments, the method for obtaining synthetic feedstock comprises: (a) heating the plastic at a temperature between about 400° C. and about 850° C. under substantially oxygen-free conditions to produce a pyrolysis effluent; (b) condensing the pyrolysis effluent to obtain synthetic feedstock; (c) recovering the synthetic raw materials.

[0035] In some embodiments, the method of obtaining the synthetic feedstock is in the presence or absence of a catalyst. In some embodiments, after condensation, the effluent is optionally distilled. In some embodiments, recovering the synthetic feedstock involves separating or quenching the pyrolysis effluent, or both separating and quenching, to obtain the synthetic feedstock.

[0036] The pyrolysis process produces a range of hydrocarbon products from gases (having 5 or less carbons at temperatures between 10°C and 50°C and 0.5 to 1.5 atmospheres), low boiling liquids (such as gasoline or naphtha (40-200°C) or diesel fuel (180-360°C)), high (e.g., at 250-475°C) boiling liquids (oils and waxes), and some solid residues, commonly referred to as char. Char is the material remaining after the pyrolysis process is completed and the reactor effluent is collected. Char contains additives and contaminants that entered the system as part of the feedstock. Char can be a powdery residue or material similar to sludge with heavy oil components. Glass, metals, calcium carbonate / oxide, clay, and carbon black are just a few of the contaminants and additives that remain after the conversion process is completed and become part of the char.

[0037] In some embodiments, the pyrolysis reaction produces 2-30% gas (C1-C4 hydrocarbons), (2) 10-50% oil (C5-C15 hydrocarbons), (3) about 10-40% wax (≧C16 hydrocarbons), and (4) about 1-5% char. After completion of the pyrolysis process, the pyrolysis product or oil may range from 60-80% by weight C5-C15, 20-35% by weight C16-C29, and 5% or less by weight ≧C30. In some embodiments, the pyrolysis product or oil may range from 70-80% by weight C5-C15, 20-35% by weight C16-C29.

[0038] The hydrocarbons obtained from the pyrolysis of waste plastics are a mixture of alkanes, alkenes, olefins, and diolefins or polyenes, where the olefin groups are generally C1-C2, i.e., alpha-olefins, some alk-2-enes are also produced, and the dienes are generally in the alpha and omega positions, i.e., alk-α,ω-dienes, or may be conjugated dienes. In some embodiments, the pyrolysis of plastics produces paraffinic compounds, isoparaffins, olefins, diolefins, naphthenes, and aromatic compounds. In some embodiments, the proportion of 1-olefins in the pyrolysis effluent is about 25-75 wt%, or 35-65 wt%. In some embodiments, the synthetic feedstock is 25-70 wt% olefins and diolefins, 35-65 wt% olefins and diolefins, 35-60 wt% olefins and diolefins, or 5-50 wt% olefins and diolefins.

[0039] Depending on the processing conditions, the synthetic raw material can have similar characteristics to crude oil from petroleum sources, but can have various amounts of olefins and diolefins. In some embodiments, the synthetic raw material derived from waste plastics contains 35 - 65% olefins and diolefins, 10 - 50% paraffins and isoparaffins, 5 - 25% naphthenes, and 5 - 35% aromatic compounds. In some embodiments, the synthetic raw material has a carbon chain length that is about 15 - 20 wt% C9 - C16, 75 - 87 wt% C16 - C29, and about 2 - 5% C30+, and the carbon chain is mainly a mixture of alkanes, alkenes, and diolefins. In other embodiments, the synthetic raw material has 10 wt% <C12, 25 wt% C12 - C20, 30 wt% C21 - C40, and 35 wt% >C41, and the carbon chain is mainly a mixture of alkanes, alkenes, and diolefins. In still other embodiments, the synthetic raw material has about 60 - 80 wt% C5 - C15, about 20 - 35 wt% C16 - C29, and about 5 wt% or less ≥C30, and the carbon chain is mainly a mixture of alkanes, alkenes, and diolefins. In some embodiments, the synthetic raw material has about 70 - 80 wt% C5 - C15 and about 20 - 35 wt% C16 - C29, and the carbon chain is mainly a mixture of alkanes, alkenes, and diolefins.

[0040] In some embodiments, the synthetic raw material composition can have a range of α or ω olefin monomer components (e.g., α olefins or α,ω diolefins) that can react and precipitate from the synthetic raw material composition at a temperature higher than its desired temperature, or during storage, transportation, or use temperature.

[0041] When the pyrolysis oil (pyrolysis product) is stored for a long time, the storage container begins to accumulate a film. This film is formed with or without the presence of air (oxygen). Film formation is accelerated at elevated temperatures, but is formed over time at room temperature.

[0042] In some embodiments, the contaminants in the synthetic feedstock are tarry deposits or film-like contaminants and combinations thereof. In some embodiments, the tarry deposits are a solid viscoelastic material and a dark brown or black viscous liquid, each resulting from the pyrolysis of waste plastics. In some embodiments, the tarry deposits are a suspension of small black particles in a dark brown or black viscous liquid, which has the consistency of soft artist's modeling clay. In some embodiments, the tarry deposits and the film have the same infrared spectroscopic characteristics.

[0043] In some embodiments, the contaminant (e.g., as a solid viscoelastic material) comprises a polyamide with additional carboxylic acid and hydroxyl functional groups and has an elemental composition of 62-75% carbon, 6-9% hydrogen, 3-7% nitrogen, and 12-25% oxygen. In some embodiments, the elemental composition of the contaminant is 62-75% carbon, 6-9% hydrogen, 3-7% nitrogen, and 12-25% oxygen, and less than 0.3% sulfur. In some embodiments, the contaminant present in the pyrolysis oil is a secondary amide that also contains hydroxyl and carbonyl functional groups in addition to those associated with the amide functional groups. In some embodiments, the contaminant is a polyamide with long chain aliphatic groups, carboxylic acid groups, amide groups, aromatic groups with small amounts of olefinic unsaturation, and combinations thereof. Contaminant analysis is by using a two-stage gas chromatography / mass spectrometry (GC / MS) technique, the first stage being GC / MS of the volatile components collected by thermal desorption, and the second stage being GC / MS of the volatile by-products resulting from the thermal decomposition of the non-volatile fraction of the contaminant. In some embodiments, the first stage reveals that the contaminants are polyamides with long chain aliphatic groups, carboxylic acid groups, amide groups, aromatic groups with olefinic unsaturation, alkenes, alkanes, benzoic acid, caprolactam, toluene, xylene, cresol, phenol, isopropylphenol, tert-butylphenol and di-tert-butylphenol, dimethylphenol, naphthalenol, alkenes and alkanes of various lengths, and combinations thereof. Meanwhile, the second stage reveals that the major fragments identified were propylene, toluene, caprolactam, pentene, and butane. Minor fragments included tetramethylindole, ethylbenzene, ethyldimethylpyrrolole, dimethylfuran, and tetrahydroquinoline.In some embodiments, the contaminants include nylon, polyvinyl chloride (PVC), polyethylene terephthalate (PET), polyamides, caprolactam, benzoic acid, phenol, p-cresol, dimethylphenol, isopropylphenol, tert-butylphenol, dimethylethylphenol, naphthalenol, alkenes and alkanes of various lengths, propylene, toluene, pentene, butane, tetramethylindole, ethylbenzene, ethyldimethylpyrrole, dimethylfuran, tetrahydroquinoline, and combinations thereof.

[0044] Antifouling agents are added to the pyrolysis product process stream or pyrolysis product to reduce or prevent foulant formation or deposition in the pyrolysis product or process equipment. In some embodiments, the antifouling agent is an anhydride of a carboxylic acid or a derivative thereof. In some embodiments, the carboxylic acid anhydride includes succinic anhydride, maleic anhydride, acetic anhydride, phthalic anhydride, benzoic anhydride, acrylic anhydride and methacrylic anhydride and derivatives thereof.

[0045] In some embodiments, the antifouling agent is a succinic anhydride of general formula I: [ka] In the formula, R 1 is hydrogen or 8 to 36 carbon atoms, and R is 12 to 24 carbon atoms. 1 may be linear or branched, or a combination of both structures. In some embodiments, R 1 is an aliphatic alkyl or alkenyl group containing 8 to 36 carbon atoms. In some embodiments, R 1 is an aliphatic straight alkenyl chain of 8 to 36 carbon atoms.

[0046] In some embodiments, the succinic anhydride compounds include succinic acid, succinamide, succinimide, and N-alkyl, N-alkenyl, N-aryl, and N-alkaryl succinimide or alkenyl succinic anhydride. The succinic anhydride compounds include tridecyl succinic anhydride, pentadecyl succinic anhydride, tetradecyl succinic anhydride, hexadecenyl succinic anhydride, dodecyl succinic anhydride, tetradecyl succinic anhydride, hexadecenyl succinic anhydride, octadecyl succinic anhydride, dodecyl succinic anhydride, and mixtures thereof. In some embodiments, the antifouling agent is succinic anhydride, alkenyl succinic anhydride. In some embodiments, the antifouling agent is selected from dodecenyl succinic anhydride (DDSA), also known as tetrapropenyl succinic anhydride (TPSA), maleic anhydride and alpha-olefin copolymers, or combinations thereof.

[0047] In some embodiments, the antifouling agent is a polymer. In some embodiments, the polymer is a polymerized copolymer of an unsaturated or saturated monomer and an olefin. In some embodiments, the olefin is an alpha olefin having the structure shown as Formula II: [ka] In the formula, R 1 , R 2 , R 3 , and R 4 are independently hydrogen and C 5 ~C 60 A blend of two or more such alpha olefin monomers having formula (I), with the proviso that at least two of them are hydrogen, is suitable for inclusion in a copolymer. In some embodiments, R 1 , R 2 , R 3 , and R 4 are independently hydrogen or C 12 ~C 60The maleic anhydride monomer has the formula III: [ka] In the formula, R 5 and R 6 are each independently selected from hydrogen or an alpha olefin or styrene as described above.

[0048] In some embodiments, the alpha-olefin has 10-36 carbons, or 14-32 carbons, or 18-30 carbons, or 24-28 carbons, the number of carbons being an average number reflecting a blend of compounds, or a substantially single value determined by the user. The polymer comprises a weight ratio of alpha-olefin residue to maleic anhydride residue of about 1:1 to about 1:5. The weight average molecular weight (M,) of the copolymer is about 5,000 g / mol to about 100,000 g / mol, 5,000 g / mol to about 25,000 g / mol, and about 5,000 g / mol to about 15,000 g / mol, as analyzed by gel permeation chromatography. The copolymer is synthesized using conventional techniques, such as radical addition polymerization principles and techniques well known to those skilled in the art of polymer synthesis. The polymer is further analyzed using conventional methodologies well known to polymer chemists, including gel permeation chromatography and infrared analysis, to ensure that the target structure and molecular weight are achieved in the precursor polymer.

[0049] The antifouling agent may be in the form of a concentrate comprising about 15% to 90% by weight, or about 15% to 85% by weight, or about 15% to 80% by weight, or about 15% to 75% by weight, or about 15% to 70% by weight, or about 15% to 65% by weight, or about 15% to 60% by weight, or about 15% to 55% by weight, or about 15% to 50% by weight, or about 15% to 45% by weight, or about 15% to 40% by weight, or about 15% to 35% by weight, or about 15% to 30% by weight, or about 15% to 25% by weight, or about 20% to 80% by weight, or about 30% to 50% by weight, or about 50% to 90% by weight, or about 50% to 80% by weight of the antifouling agent described above.

[0050] The antifouling agent is an antifouling agent having a concentration of about 10 ppm to 5000 ppm by weight, or about 10 ppm to 1000 ppm, or 900 ppm to 5,000 ppm, or about 10 ppm to 500 ppm, or about 20 ppm to 500 ppm, or about 30 ppm to 500 ppm, or about 40 ppm to 500 ppm, or about 50 ppm to 500 ppm, or about 60 ppm to 500 ppm, or about 70 ppm to 500 ppm, or about 80 ppm to 500 ppm, or about 90 ppm to 500 ppm, or about 100 ppm to 500 ppm, or about 400 ppm to 5000 ppm, or about 5 ppm to 450 ppm, or about 5 ppm to 400 ppm, or When added to a synthetic pyrolysis stream or synthetic pyrolysis product in an amount corresponding to about 5 ppm to 350 ppm, or about 5 ppm to 300 ppm, or about 5 ppm to 250 ppm, or about 5 ppm to 200 ppm, or about 5 ppm to 150 ppm, or about 5 ppm to 100 ppm, or about 10 ppm to 300 ppm, or about 10 ppm to 250 ppm, or about 50 ppm to 250 ppm, or about 50 ppm to 200 ppm, or about 100 ppm to 200 ppm, or about 100 ppm to 5000 ppm of the antifoulant, it is effective to reduce or prevent fouling and form a treated synthetic pyrolysis stream or a treated synthetic pyrolysis product.

[0051] The treated synthetic pyrolysis stream comprises between about 10 ppm and 5000 ppm total by weight of the antifoulant composition. The treated synthetic pyrolysis product is a product comprising between about 10 ppm and 5000 ppm total by weight of the antifoulant. The treated synthetic pyrolysis process stream is a synthetic pyrolysis product disposed within a synthetic pyrolysis processing equipment and comprising between about 10 ppm and 5000 ppm total by weight of the antifoulant composition.

[0052] In some embodiments, the treated synthetic pyrolysis process stream experiences substantially less fouling of contacted synthetic pyrolysis processing equipment during one or more synthetic pyrolysis processing operations than a corresponding untreated synthetic pyrolysis process stream, and reduction or prevention of fouling is observed within the synthetic pyrolysis process stream or streams, during disposal of the treated synthetic pyrolysis process stream in one or more petroleum processing units, or during storage of the synthetic pyrolysis products in a storage vessel.

[0053] Thus, disclosed herein is a method of reducing fouling in one or more synthetic pyrolysis process streams, comprising, consisting essentially of, or consisting of applying about 10 ppm to 5000 ppm by weight or volume of an antifoulant to the synthetic pyrolysis process stream to form a treated synthetic pyrolysis process stream. The antifoulant composition comprises, consists essentially of, or consists of one or more combinations of antifoulants or antifoulant polymers, where the antifoulant is tetrapropylene succinic anhydride and the antifoulant polymer is a reaction product of maleic anhydride and an alpha olefin. Any of the compositions described above are useful in conjunction with the method of reducing fouling, the method comprising applying about 10 ppm to 5000 ppm by weight or volume of an antifoulant composition to the synthetic pyrolysis process stream to form a treated synthetic pyrolysis process stream.

[0054] Antifoulants are useful in preventing or reducing the deposition of contaminants in process equipment, such as quench towers or columns used in synthetic feedstock production processes. In some embodiments, the antifoulant is added to the feedstock (refined or unrefined) or combinations thereof that are held in storage during the production of synthetic feedstock. The antifoulant can be added at one or more points in the process. In some embodiments, the antifoulant is added at the point where the gaseous pyrolysis products begin to condense, allowing the antifoulant to travel with the condensed pyrolysis products and achieve contact with contaminants that have precipitated or would otherwise precipitate in the absence of the antifoulant. In some embodiments, the antifoulant is added to the inlet or outlet of the quench tower, or to the pyrolysis product storage, or to the quench tower or column and pyrolysis product storage or drum. For example, the antifoulant is added at a point in the process as shown in FIG. 3.

[0055] In some embodiments, the antifoulant is added at the inlet of a quench tower or column, or an air- or water-cooled condenser, when the synthetic feed vapors exiting the pyrolysis reactor are quenched and the gases are cooled and condensed at a temperature of about 100° C. to 200° C., or about 110° C. to 140° C., or about 105° C. to 120° C. In some embodiments, the antifoulant is added to the synthetic feed held in storage.

[0056] In certain embodiments, a filtering step may be performed before and / or after any of the above locations. Filtering steps may be useful in those embodiments where the antifouling agent interacts with the film-forming components to create adducts. In some pyrolysis oils, these adducts are soluble, but in certain pyrolysis oils, the adducts are insoluble. In such cases, for example, the antifouling agent may prevent adhesion of the film-forming components to the storage container. In an illustrative embodiment, the filtering step is performed after the formation of the pyrolysis oil and / or after the addition of the antifouling agent, but before further processing of the pyrolysis oil.

[0057] The antifouling agent may be added by any suitable method. For example, the antifouling agent may be added neat or with an adjuvant. In some embodiments, the adjuvant is a solvent or other dispersing agent (e.g., a surfactant). In some embodiments, the antifouling agent may be applied as a solution that is sprayed, dripped, or injected into desired openings in the system or onto the process equipment or fluids contained therein. The antifouling agent may be added continuously, intermittently, or batchwise to the process equipment as needed.

[0058] The antifoulant is applied to process equipment to form treated process equipment, and in some embodiments, the treated process equipment may be observed to experience less foulant build-up than process equipment without the addition of the antifoulant.

[0059] The reduction or prevention of contaminant formation or deposition can be evaluated by any known method or test, such as, for example, ASTM D4625. In some embodiments, synthetic feedstocks treated with antifouling agents have a reduction in contaminant contamination of about 5%-95%, 5%-75%, 5%-50%, 5%-25%, 5%-15%, 50%-95%, 50%-20%, or 50%-75%.

[0060] Other additives can be added to the pyrolysis oil during processing and storage. In some embodiments, the other additives are antioxidants, paraffin inhibitors, asphaltene dispersants, wax dispersants, tar dispersants, neutralizing agents, surfactants, biocides, preservatives, or any combination thereof. In some embodiments, the other additives are antioxidants, pour point depressants, or extraction solvents added to the pyrolysis oil, or combinations thereof. For example, antioxidants added include the antioxidants reported in U.S. Provisional Patent Application No. 63 / 159266, the pour point depressants reported in U.S. Provisional Patent Application No. 63 / 078111, and the extraction solvents reported in U.S. Provisional Patent Application No. 63 / 168643. Each of the reported applications is incorporated herein by reference in its entirety. EXAMPLES

[0061] The following examples are intended to illustrate different aspects and embodiments of the present invention and should not be considered as limiting the scope of the invention. It will be appreciated that various modifications and variations can be made without departing from the scope of the claims.

[0062] Example 1. Contaminant characterization

[0063] Elemental (CHNS) analysis was performed on a sample of the contaminant film obtained from the pyrolysis oil. The film was separated from the pyrolysis oil, washed with heptane, and then dissolved in dichloromethane. The dichloromethane was evaporated to leave the contaminant residue.

[0064] Table 1 shows the CHNS analysis.

[0065] [Table 1]

[0066] Contaminant samples from the different pyrolysis sources were also evaluated by infrared (IR) spectroscopy. IR spectra were evaluated using a Nicolet iS50 FTIR equipped with an on-board diamond internal reflectance accessory. Spectra were run at four wavenumber resolution and were the result of 32 simultaneous additive scans.

[0067] IR spectroscopy showed the presence of long chain aliphatic groups, carboxylic acid groups, amide groups, and aromatic groups with small amounts of olefinic unsaturation. The major components of the contaminants were secondary amides (e.g., polyamides). See Figure 4, which shows that the contaminants in the various samples showed similar compositions with some variation in the amounts of aliphatic hydrocarbons, carboxylic acids, amides, and aromatic compounds among the groups. The contaminant compositions within the samples showed similar compositions at different temperatures.

[0068] The thermal profiles of various pyrolysis samples from different sources were analyzed by evolved gas analysis. The samples were heated at 600 °C. The volatile fractions of the samples were thermally desorbed at temperatures between 40 °C and 300 °C, chromatographically separated by gas chromatography, and detected by mass spectrometry.

[0069] Figure 5 shows the off-gas analysis and desorption products of contaminants from the pyrolysis products. The volatile components identified showed a predominance of caprolactam with minor amounts of benzoic acid, phenol, p-cresol, dimethylphenol, isopropylphenol, tert-butylphenol, dimethylethylphenol, naphthalenol, and alkenes and alkanes of various lengths. Heating the sample at 600°C pyrolyzes the sample into various fragments. The major fragments identified were propylene, toluene, caprolactam, pentene, and butane. Minor fragments included tetramethylindole, ethylbenzene, ethyldimethylpyrrole, dimethylfuran, and tetrahydroquinoline.

[0070] Example 2. Stability of Contaminants from Plastic Pyrolysis The stability of the synthetic raw materials was evaluated in the presence or absence of various soil release agents, namely soil release agent 1 (15% maleic anhydride-C24-C28 alpha-olefin copolymer, CAS number 68459-79-0) or soil release agent 2 (tetrapropylene-succinic anhydride, CAS number 26544-38-7), at various concentrations and different temperatures. The stability was tested by ASTM D4626 (4 weeks storage at 25°C and 43°C). Untreated samples (without added soil release agents) at 25°C and 43°C served as controls.

[0071] Antifouling agents were tested on various pyrolysis feedstocks: pyrolysis feedstock sample 1 (60-80 wt% C5-C15, 20-35 wt% C16-C29, and 5 wt% or less ≧C30), and pyrolysis feedstock sample 2 (70-80 wt% C5-C15, 20-35 wt% C16-C29). The pyrolysis feedstocks treated with various antifouling agents were collected and divided into several portions for stability testing over a period of one month at 25°C or 43°C according to ASTM D4625 procedural guidelines. The samples were observed for one month at high temperature and for three months at room temperature. The storage stability results with antifouling agent 1 and antifouling agent 2 are shown in Table 2. [Table 2]

[0072] Example 3. Thermogravimetric analysis

[0073] Thermo-gravimetry analysis (TGA) of the films formed after stability testing of various pyrolysis products was performed to determine the thermal decomposition temperature (Td) and residue analysis. The non-volatile matter after TGA study up to 600 °C was quantified and is shown in Table 3. The TGA was performed in an inert gas (e.g., N 2 ) to minimize the formation of oxidation by-products (combustion). [Table 3]

[0074] By 600°C, all samples show approximately 90% decomposition or volatilization. However, 18-31% of the film or residue does not volatilize at temperatures up to 600°C. In other words, the film or residue is completely volatilized in the convection section. The film composition (e.g., mainly caprolactam, aromatics) determines non-volatility in TGA experiments. Residue analysis with antifoulant 1 reduces non-volatiles to 4-12%. No residue was left when 100% active antifoulant 2 was used. Thus, antifoulant 2 is effective as film formation is mitigated in sample 2 pyrolysis product without solid precipitation.

[0075] All of the compositions and methods disclosed and claimed herein can be made and executed without undue experimentation in light of the present disclosure. The present invention can be embodied in many different forms, and certain preferred embodiments of the present invention are described in detail herein. The present disclosure is an exemplification of the principles of the present invention and is not intended to limit the invention to the specific embodiments illustrated. In addition, unless expressly stated otherwise, the term "a" is intended to include "at least one" or "one or more." For example, "a device" is intended to include "at least one device" or "one or more devices."

[0076] Any ranges expressed in either absolute or approximate terms are intended to encompass both, and any definitions used herein are intended to be illustrative, not limiting. Notwithstanding that the numerical ranges and parameters setting forth the broad scope of the invention are approximations, the numerical values ​​set forth in the specific examples are reported as precisely as possible. However, any numerical value inherently contains certain errors necessarily resulting from the standard deviation found in their respective testing measurements. Moreover, all ranges disclosed herein should be understood to encompass any and all subranges subsumed therein, including all fractional and whole values.

[0077] Any composition disclosed herein can comprise, consist of, or consist essentially of any element, component, and / or ingredient disclosed herein, or any combination of two or more of the elements, components, or ingredients disclosed herein.

[0078] Any method disclosed herein may comprise, consist of, or consist essentially of any method steps disclosed herein, or any combination of two or more of the method steps disclosed herein.

[0079] The transitional phrase "comprising," which is synonymous with "including," "containing," or "characterized by," is inclusive or open-ended and does not exclude additional, unrecited elements, components, ingredients, and / or method steps.

[0080] The transitional phrase "consisting of" excludes any element, component, ingredient, and / or method step not specified in the claim.

[0081] The transitional phrase "consisting essentially of" limits the scope of the claim to certain elements, components, ingredients, and / or steps, and those that do not materially affect the basic and novel characteristics of the claimed invention.

[0082] Unless otherwise specified, all molecular weights referred to herein are weight average molecular weights and all viscosities were measured at 25° C. using neat (undiluted) polymer.

[0083] As used herein, the term "about" refers to a cited value that is within error resulting from the standard deviation found in their respective testing measurements; where such error cannot be determined, "about" may refer, for example, to within 5%, 4%, 3%, 2%, or 1% of the cited value.

[0084] Moreover, the present invention encompasses all possible combinations of any or all of the various embodiments described herein. It should also be understood that various changes and modifications to the preferred embodiments of the invention described herein will be apparent to those skilled in the art. Such changes and modifications can be made without departing from the spirit and scope of the present invention and without diminishing its intended advantages. Accordingly, such changes and modifications are intended to be covered by the appended claims.

Claims

1. 1. A method for reducing or preventing contamination in a plastic-derived synthetic feedstock composition, the method comprising:

1. A method comprising adding an antifouling agent comprising a carboxylic acid anhydride or a copolymer of a dicarboxylic acid anhydride and an alpha olefin to a synthetic feedstock composition derived from plastic pyrolysis containing contaminants to provide a treated pyrolysis product.

2. The method of claim 1 , wherein the synthetic feedstock comprises pyrolysis oil.

3. 3. The method of claim 1 or 2, wherein the synthetic feedstock comprises about 60-80 wt% C5-C15, about 20-35 wt% C16-C29, and about 5 wt% or less > C30.

4. 3. The method of claim 1 or 2, wherein the carboxylic acid anhydride is succinic anhydride, maleic anhydride, acetic anhydride, phthalic anhydride, benzoic anhydride, acrylic anhydride, and methacrylic anhydride, derivatives thereof, and any combination thereof.

5. 3. The method of claim 1, wherein the antifouling agent is tetrapropylene-succinic anhydride or dodecenyl succinic anhydride.

6. The method of claim 1 or 2, wherein the copolymer comprises maleic anhydride and an alpha olefin.

7. 3. The method of claim 1 or 2, wherein the antifouling agent is added at the inlet of the quench tower, at the outlet of the quench tower, to a storage vessel containing pyrolysis products, after production of pyrolysis oil, and any combination thereof.

8. The method of claim 1 or 2, wherein the antifouling agent is added at about 10 ppm to 5,000 ppm.

9. 3. The method of claim 1 or 2, wherein the contaminants comprise nylon, polyvinyl chloride (PVC), polyethylene terephthalate (PET), polyamide, caprolactam, benzoic acid, phenol, p-cresol, dimethylphenol, isopropylphenol, tert-butylphenol, dimethylethylphenol, naphthalenol, alkenes and alkanes of various lengths, propylene, toluene, pentene, butane, tetramethylindole, ethylbenzene, ethyldimethylpyrrole, dimethylfuran, tetrahydroquinoline, and combinations thereof.

10. 3. The method of claim 1 or 2, wherein the synthetic feedstock composition further comprises an antioxidant, a pour point depressant, an extraction solvent, or any combination thereof.

11. The synthetic raw material derived from plastic pyrolysis, (a) heating a plastic at a temperature of about 400°C to about 850°C under substantially oxygen-free conditions to produce a pyrolysis effluent; (b) cooling and condensing the pyrolysis effluent to obtain synthetic feedstock; 3. The method of claim 1 or 2, wherein the synthetic raw material is obtained by a process comprising: (c) recovering the synthetic raw material.

12. 12. The method of claim 11, further comprising cooling the recovered synthetic feed in a quench tower, an air-cooled condenser, or a water-cooled condenser.

13. 12. The method of claim 11, wherein the synthetic material comprises polyethylene, polypropylene, polystyrene, and any combination thereof.

14. A composition comprising a synthetic material derived from plastic, the synthetic material comprising: (a) heating a plastic at a temperature of about 400°C to about 850°C under substantially oxygen-free conditions to produce a pyrolysis effluent; (b) cooling and condensing the pyrolysis effluent to obtain synthetic feedstock; (c) recovering the synthesis raw materials; (d) adding a soil release agent to said synthetic stock composition to provide a treated synthetic stock; (e) separating the treated synthetic feedstock to obtain a synthetic feedstock having reduced contaminants.

15. 15. The composition of claim 14, wherein the synthetic feedstock comprises about 60-80 wt% C5-C15, about 20-35 wt% C16-C29, and up to about 5 wt% > C30.

16. 16. The composition of claim 14 or 15, wherein the soil release agent comprises a carboxylic acid anhydride or a copolymer of a dicarboxylic acid anhydride and an alpha olefin.

17. 16. The composition of claim 14 or 15, wherein the antifouling agent is tetrapropylene-succinic anhydride or the antifouling agent comprises a copolymer of maleic anhydride and an alpha olefin.

18. 16. The composition of claim 14 or 15, wherein the synthetic feedstock composition further comprises an antioxidant, a pour point depressant, an extraction solvent, or any combination thereof.

19. 1. A treated synthetic pyrolysis product comprising a synthetic raw material, a contaminant, and an antifouling agent, wherein the antifouling agent is a copolymer comprising a carboxylic acid anhydride or a dicarboxylic acid anhydride and an alpha olefin.

20. 20. The processed synthetic pyrolysis product of claim 19, wherein the synthetic feedstock comprises about 60 to about 80 wt% C5-C15, about 20 to about 35 wt% C16-C29, and about 5 wt% or less > C30.

21. 3. Use of the antifouling agent according to claim 1 or 2 to prevent fouling in synthetic materials originating from plastics.

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