Crumb rubber obtained from recycled tires is subjected to an interlinked substitution process. The process utilizes a reactive component that interferes with sulfur bonds. The resulting treated rubber exhibits properties similar to those of the virgin composite rubber structure prior to being granulated, and is suitable for use in fabricating new tires, engineered rubber articles, and asphalt rubber for use in waterproofing and paving applications.

A method is provided for deconstructing macromolecules (MM) into lower molecular weight (MW) fragments in high yield by promoting first desirable reactions (Reactions1) that result in chemolytic scission of bonds in the backbone, chain, matrix, or network that defines the MM and obtain a first product mixture (Product1). The method includes conveying the prepared feedstock in a flowpath toward a reactor while adding a first agent of a first type (A1T1) suitable for promoting Reactions1, and a second agent (A2) suitable for promoting Reactions1 to obtain a first reaction mixture which is heated under controlled pressure.

A method for recycling polyester from a polyester textile. The method comprises the steps of: providing said polyester textile soaked in a mixture comprising a solvent and a catalyst, providing and maintaining a temperature of said mixture comprising said polyester textile within a range of 80-240° C. during depolymerization of polyester in said polyester textile and wherein, in said step of providing said polyester textile soaked in said mixture, said catalyst of said mixture comprises calcium hydroxide. A catalyst may be used for depolymerization of polyester in a polyester textile, wherein the catalyst comprises calcium hydroxide. Natural fibers may be recovered from a textile comprising polyester and natural fibers.

The present invention relates to the field of recycling PET-type plastics commonly used for the manufacture of disposable plastic bottles, food trays, textiles, etc. More specifically, it relates to a method for converting PET into dimethyl terephthalate (DMT) in a few hours (less than 5 hours) by means of a complete reaction resulting in a product free of impurities. The depolymerisation step is carried out in the presence of a monoalcohol as well as an organic base with a guanidine or amidine unit, and a second base which may be either an inorganic base or an ether oxide. These two bases are present in catalytic amounts relative to the amount of PET to be treated.

The present invention relates to the field of recycling PET-type plastics commonly used for the manufacture of disposable plastic bottles, food trays, textiles, etc. More specifically, it relates to a method for converting PET into dimethyl terephthalate (DMT) in a few hours (less than 5 hours) by means of a complete reaction resulting in a product free of impurities. The depolymerisation step is carried out in the presence of a monoalcohol as well as an organic base with a guanidine or amidine unit, and a second base which may be either an inorganic base or an ether oxide. These two bases are present in catalytic amounts relative to the amount of PET to be treated.

Described herein are methods for rendering biodegradable a plastic material that is not itself biodegradable, by blending the plastic material with a carbohydrate-based polymeric material that is formed from a) one or more starches and a plasticizer (e.g., glycerin), b) an additive known in the art as an OXO material and/or an additive that interacts with microbes that contribute to biodegradation of the non-biodegradable material. The carbohydrate-based polymeric material is less crystalline than the non-biodegradable materials, e.g., being substantially amorphous, and having a crystallinity of no more than 20%. When tested under conditions causing biodegradation, the blend biodegrades to an extent greater than the content of the carbohydrate-based polymer.

Described herein are methods for rendering biodegradable a plastic material that is not itself biodegradable, by blending the plastic material with a carbohydrate-based polymeric material that is formed from a) one or more starches and a plasticizer (e.g., glycerin), b) an additive known in the art as an OXO material and/or an additive that interacts with microbes that contribute to biodegradation of the non-biodegradable material. The carbohydrate-based polymeric material is less crystalline than the non-biodegradable materials, e.g., being substantially amorphous, and having a crystallinity of no more than 20%. When tested under conditions causing biodegradation, the blend biodegrades to an extent greater than the content of the carbohydrate-based polymer.

The present disclosure relates to a composition that includes a lignin-derived mixture that includes at least one of a dimer, a trimer, and/or a tetramer, where the composition is characterized by a thermal stability up to a maximum temperature between about 260° C. and about 300° C.

The present disclosure relates to a composition that includes a lignin-derived mixture that includes at least one of a dimer, a trimer, and/or a tetramer, where the composition is characterized by a thermal stability up to a maximum temperature between about 260° C. and about 300° C.

Provided is a reinforcing material having high interfacial adhesion with a matrix resin. The reinforcing material containing a covering layer according to an embodiment of the present invention includes a reinforcing material that imparts strength to a matrix resin by being combined with the matrix resin, and a covering layer formed on a surface of the reinforcing material, in which the covering layer is formed of a vaporized material generated by heating the resin.