Abstract: The embodiments relate to a heat shrinkable film and a process for regenerating a polyester container using the same. The heat shrinkable film comprises a copolymerized polyester resin comprising a diol component and a dicarboxylic acid component and has a heat shrinkage rate of 30% or more in the main shrinkage direction upon thermal treatment at a temperature of 80° C. for 10 seconds, a melting point of 190° C. or higher as measured by differential scanning calorimetry, and a peak temperature (Tp) of 95° C. to 115° C. as measured in the endothermic and exothermic curve (heat flow) by differential scanning calorimetry. It not only solves the environmental problem by improving the recyclability of the polyester container, but also is capable of enhancing the yield and productivity.

Abstract: An improved method forms and employs a wax to modify asphalt. The method includes: (a) selecting a solid polymeric material, (b) heating the solid polymeric material in an extruder to produce a molten polymeric material, (c) filtering the molten polymeric material, (d) placing the molten polymeric material through a chemical depolymerization process in a reactor to produce a depolymerized polymeric material, and (e) adding the depolymerized material to a pre-wax mixture to produce a polymer-modified asphalt. The addition of wax reduced the mixing time necessary to achieve improved polymer dispersion compared to the control formulation modified bitumen and reduced the viscosity of the neat bitumen. Pre-polymer addition of wax is detrimental to most properties of the resulting modified asphalt. Post-polymer addition improved viscosity reduction, higher softening point and improved dimensional stability.

Abstract: A hyperbranched boric acid modified phthalonitrile monomer as well as a preparation method and use thereof are provided. The preparation method of the hyperbranched boric acid modified phthalonitrile monomers includes: a reaction in the mixture containing a boron source, a phenol compound, and a solvent to prepare a compound with a B—O structure; and a reaction in the mixture containing the compounds with the B—O structure, 4-nitrophthalonitrile, a catalyst, and a solvent to prepare the hyperbranched boric acid modified phthalonitrile monomers.

Abstract: A semicrystalline poly ketone powder useful for additive manufacturing may be made by dissolving a polyketone having differential scanning calorimetry (DSC) monomodal melt peak, at a temperature above 50° C. to below the melt temperature of the polyketone, precipitating the dissolved polyketone by cooling, addition of a nonsolvent or combination thereof. The method may be used to form polyketones having a DSC melt peak with an enthalpy greater than the starting polyketone.

Abstract: A polyester resin containing: a diol constituent unit containing a unit a1 derived from spiroglycol represented by formula (1) and a unit a2 derived from ethylene glycol; and a dicarboxylic acid constituent unit containing a unit b derived from terephthalic acid and/or an ester thereof. A content of the unit a1 is from 5 to 60 mol % and a content of the unit a2 is from 30 to 95 mol %, based on a total amount of the unit a1 and the unit a2. A content of the unit b is from 80 to 100 mol % based on a total amount of the dicarboxylic acid constituent unit.

Abstract: The present invention relates to the flotation of non-sulfidic minerals and ores. Particularly the present invention relates to a collector for the beneficiation of non-sulfidic minerals and ores.

Abstract: The present invention is directed to a curable and one component (1K) debondable adhesive composition comprising: a) epoxy resin; b) a curing agent for said epoxy resin; c) an electrolyte; and, d) an electrically non-conductive filler; wherein said composition comprises at least one of: e) a combination of a solubilizer and a toughener; and, f) electrically conductive particles.

Abstract: The present invention relates to a method for preparing a polyester carbonate starting from cycloaliphatic diacids and aliphatic diols and to the polyester carbonate prepared by the method. The method according to the invention is a direct synthesis in which all the structural elements that form the subsequent polyester carbonate are already present as monomers in the first step of the method.

Abstract: There are provided processes for recycling polystyrene waste. The processes can comprise dissolving said polystyrene waste in ethylbenzene under conditions to obtain a polystyrene/ethylbenzene mixture, adding the polystyrene/ethyl benzene mixture to a hydrocarbon polystyrene non-solvent under conditions to obtain precipitated polystyrene and washing the precipitated polystyrene with additional portions of hydrocarbon polystyrene non-solvent under conditions to obtain twice-washed polystyrene. The twice-washed polystyrene can optionally be dried and formed into polystyrene pellets. There is also provided recycled polystyrene obtained from such processes for recycling polystyrene waste.

Abstract: Methods of depolymerizing polyolefin-based material into useful petrochemical products using styrene oligomers or polymers, and heat are described. The styrene oligomers or polymers improve the depolymerization reaction by decreasing the halftime for the depolymerization, which results in a higher depolymerization rate and a shorter residence time in the depolymerization unit, allowing for a predictable depolymerization reaction, and decreasing the branching or aromatic formations in the product.

Abstract: A method for recovering natural fibers from a textile comprising polyester and natural fibers. The method comprises the steps of: providing said textile soaked in a mixture comprising a solvent and a catalyst, providing and maintaining a temperature of said mixture comprising said textile within a range of 80-240° C. during depolymerization of polyester in said textile; and recovering natural fibers after said depolymerization, wherein, in said step of providing said textile soaked in said mixture, said catalyst of said mixture comprises calcium oxide.

Abstract: A method for synthesising polymers through devulcanisation from waste containing elastomers, the method including: a) contacting the waste containing elastomers with a solvent in the presence of a devulcanisation agent, b) heating the mixture produced in step a), at a temperature of between 20° C. and 250° C. for a period of between 15 minutes and 24 hours in the presence of a devulcanisation agent, the concentration of devulcanisation agent, and the ratio between the concentration of devulcanisation agent, expressed as parts per hundred of elastomer (phr) and a volume of solvent, expressed in ml, is: greater than 0.3 phr/ml of solvent or less than 0.2 phr/ml of solvent when the method is carried out in air, greater than 0.06 phr/ml of solvent when the method is carried out in an inert atmosphere.

Abstract: The present invention relates to a highly bio-based polycarbonate ester and a method for producing same. The highly bio-based polycarbonate ester has a bio-based carbon content of 80% or more since the highly bio-based polycarbonate ester is obtained by copolymerization of 1,4:3,6-dianhydrohexitol, which is a bio-based monomer derived from biomass, and 1,4-cyclohexanedicarboxylate and/or terephthalate, and therefore, the highly bio-based polycarbonate ester is not only human-friendly and environmentally friendly, but also advantageous in terms of biodegradability.

Abstract: A process for producing polyhydroxyalkanoates (PHA) is provided. The process comprises: providing a waste stream comprising lignocellulosic materials; adding an calcium-containing mineral to the waste stream; heat-treating the waste stream in the presence of the calcium-containing mineral, to obtain a treated waste stream; fermenting at least one strain of PHA-producing microorganism in a culture medium comprising the treated waste stream as a carbon source, to produce the PHA; and extracting the PHA from the PHA-producing microorganism.

Abstract: A curative for epoxidized plant-based oils and epoxidized natural rubber is created from the reaction between a naturally occurring polyfunctional acid and an epoxidized plant-based oil is disclosed. The curative may be used to produce porosity-free castable resins and vulcanize rubber formulations based on epoxidized natural rubber. Materials made from disclosed materials may be advantageously used as leather substitutes.

Abstract: The invention relates to a process for producing a terephthalate polyester from at least one feedstock of polyester to be recycled, integrating a process of depolymerization, advantageously by glycolysis, of the polyester to be recycled in order to produce a diester intermediate compatible with the specifications of the polymerization steps and comprising an optimized system for recycling the streams.

Abstract: The present disclosure relates to an oxidation-reduction polymer which can be used in an electrochemical sensor, and particularly, in a polymer backbone of an electron transfer medium of the electrochemical sensor. More specifically, the present disclosure relates to: an oxidation-reduction polymer which can be used in a poly (allyl glycidyl ether)-based electrochemical sensor including a repeating unit derived from allyl glycidyl ether; and an electron transfer medium and an electrochemical sensor including same, wherein the oxidation-reduction polymer is advantageous in confirming the completion of reaction during manufacture, has high immobilization efficiency of the transition metal complex, has low possibility of having problems of toxicity and side effects, and can add various functions.

Abstract: A method for degrading crosslinked superabsorbent fibers (SAF) into soluble polymers is disclosed. Degradation is achieved with an oxidative water-soluble salt comprising at least one cation and at least one anion.

Abstract: An apparatus and method for high pressure treatment of bulk material by extraction and/or impregnation may involve high pressure treating bulk material in a high pressure treatment volume of a pressure vessel apparatus at a high pressure level, especially high pressure in the range from 40 to 1000 bar. The method comprises at least the three following step sequences that are each controllable individually: pressurization, high pressure treatment, and depressurization. The high pressure treatment is performed in a continuous manner in the high pressure treatment volume. The high pressure treatment volume or the entire pressure vessel apparatus is in a fixed arrangement during the high pressure treatment. The continuity of the high pressure treatment is ensured solely by means of the high pressure treatment volume. This especially enables engineering optimization of high pressure treatment processes, for example extraction.

Abstract: The invention relates to an electrically insulating composite material (1) comprising a polyepoxide matrix (2) of cycloaliphatic type or of diglycidyl ether type in a content of less than 40% by mass, from 20 to 75% by mass of one or several micrometric and/or mesometric filler(s) (3), and from 0.1 to 20% by mass of at least one ionic liquid (4), the masses being expressed relative to the total mass of the electrically insulating composite material (1). The invention also relates to a method for manufacturing such an electrically insulating composite material (1), as well as its use for an electrically insulating support (9) in a metal-enclosed substation (5).