This disclosure relates to the production of chemicals and plastics using pyrolysis oil from the pyrolysis of plastic waste as a co-feedstock along with a petroleum-based or fossil fuel co-feed, or as a feedstock in the absence of a petroleum-based or fossil fuel co-feed. A mass balance accounting approach is employed to attribute the pounds of pyrolyzed plastic products derived from pyrolysis oil to any output stream of a given unit, which permits assigning circular product credit to product streams. In an aspect, the polymers and chemicals produced according to this disclosure can be certified under International Sustainability and Carbon Certification (ISCC) provisions as circular polymers and chemicals at any point along complex chemical reaction pathways.

The present invention relates to a process for purifying a pyrolyzed plastic waste, the process comprising the steps of providing the pyrolyzed plastic waste, wherein the pyrolyzed plastic waste is a liquid or a wax at 20° C. and 1 atm, contacting the pyrolyzed plastic waste with activated carbon yielding a pretreated 5 plastic waste and hydrogenating the pretreated plastic waste using hydrogen and a metal-based catalyst yielding a hydrogenated plastic waste suitable for steam cracking.

Systems and methods are provided for conversion of polymers (such as plastic waste) to olefins. The systems and methods can include an initial pyrolysis stage where a plastic feedstock is delivered to the initial pyrolysis stage by one or more melt extruders. The one or more melt extruders can be heated to maintain the plastic feedstock in a liquid state during delivery of the plastic feedstock to the initial pyrolysis stage. This can allow for delivery of the plastic feedstock into the pyrolysis process with a controlled distribution of plastic into the pyrolysis reactor.

Systems and methods for processing waste plastics are provided. One method includes mixing, heating and compacting a supply of the waste plastic based feedstock having an appreciable amount of halide compounds or heteroatoms from one or more sources of contamination; providing an amendment comprising alkaline earth oxides and/or hydroxides, oxides of iron, and/or oxides of aluminum to be mixed, heated and compacted with the waste plastic based feedstock to form a densified melt of plastic material including the amendment; and pyrolyzing the densified melt of plastic material including the amendment within a pyrolysis reactor. Another method includes pyrolyzing a supply of the waste plastic feedstock within a pyrolysis reactor to generate a hydrocarbon gas stream and a solids residue stream; condensing out a tars product from the hydrocarbon gas stream output from the pyrolysis reactor with a quenching apparatus; and pyrolyzing the tars product within a supplemental pyrolysis reactor.

Methods and systems are provided for the conversion of waste plastics into various useful downstream recycle-content products. More particularly, the present system and method involves integrating a pyrolysis facility with a cracker facility by introducing at least a stream of r-pyrolysis gas into the cracker facility. In the cracker facility, the r-pyrolysis gas may be separated to form one or more recycle content products, and can enhance the operation of the facility.

Chemical recycling facilities for processing mixed plastic waste are provided herein. Such facilities have the capability of processing mixed plastic waste streams and utilize a variety of recycling facilities, such as, for example, solvolysis facility, a pyrolysis facility, a cracker facility, a partial oxidation gasification facility, an energy generation/energy production facility, and a solidification facility. Streams from one or more of these individual facilities may be used as feed to one or more of the other facilities, thereby maximizing recovery of valuable chemical components and minimizing unusable waste streams.

A method is disclosed of producing hydrocarbons from a recycled or renewable organic material, wherein the recycled or renewable organic material contains from 5 to 30 wt-% oxygen as organic oxy-gen compounds and from 1 to 1000 ppm phosphorous as phosphorous compounds. Exemplary methods include (a) providing the recycled or renewable organic material (c) thermally cracking the recycled or renewable organic material thereby reducing the oxygen and phosphorous content of the recycled or renewable organic material to obtain (i) a vapor fraction containing a major part of volatiles, and (ii) a thermally cracked recycled or renewable organic material fraction containing less oxygen and less phosphorous than the recycled or renewable organic material provided in step (a); and (f) hydrotreating the thermally cracked recycled or renewable organic material fraction in a presence of a hydrotreating catalyst; to obtain hydrocarbons containing less than 1 wt % oxygen and less phosphorous than the recycled or re-newable organic material provided in step (a).

A catalytic reactor apparatus is disclosed for continuous conversion of plastic wastes into liquid fuels by dispersing a cracking catalyst in molten plastics and cracking plastic macromolecules into smaller hydrocarbons within boiling point range of gasoline and diesel fuel at temperatures significantly lower than thermal pyrolysis and thermal cracking. The catalyst/plastic mixing and heat transfer from the reactor wall to the reaction zone are enhanced using non-Newtonian stirrer. A catalytic membrane filter is used to keep the catalyst fines and unconverted plastic particulates inside the reactor while letting the desirable hydrocarbon vapor be withdrawn out of the reactor.

A method of depolymerizing polymeric material including the steps of: (a) feeding a polymeric material to a depolymerization reactor maintained at a temperature in the range of from 400° C. to 600° C. and operated under a pressure in the range of from 4 to 15 barg; and (b) depolymerizing at least a portion of the polymeric material thereby forming a first gaseous product and a first liquid product.

A non-petroleum or renewable feedstock containing oxygen and contaminants of metals, gums, and resins is treated by introducing the feedstock into a reactor at a flow velocity of at least 20 ft/sec. The feedstock is heated within the reactor and cooled to form a reduced-temperature reactor product. At least a portion of the reduced-temperature reactor product is feed into a hydroprocessing reactor containing a hydroprocessing catalyst to form a hydroprocessed product. The hydroprocessed product is cooled and non-condensable gases, metals and water are separated and removed to form a final product. The final product has an oxygen content that is 60% or less of that of the feedstock, and wherein the final product comprises 25 wt % or less any triglycerides, monoglycerides, diglycerides, free fatty acids, phosphatides, sterols, tocopherols, tocotrienols, or fatty alcohols, from 5 wt % to 30 wt % naphtha, and 50 wt % or more diesel.