Methods are disclosed for conditioning a polymeric stent after sterilization, and/or after crimping and before packaging, such that the properties of the polymeric stent fall within a narrower range of values. The stent is exposed to a controlled temperature at or above ambient for a period of time after radiation sterilization and/or after crimping and before sterilization. As a result, the polymeric stent properties, particularly radial strength and number-average molecular weight of the polymer of the polymeric stent, fall within a narrower range.

The invention mainly pertains to a method for heat treating a composition [composition (C)] which contains at least one melt-processible perfluoropolymer [polymer (F)] formed of tetrafluoroethylene (TFE) copolymer with one or more perfluorinated comonomers [comonomer (F)] containing at least one unsaturation of ethylene type in amounts from 0.5% to 13% by weight, preferably from 0.6% to 11% by weight, and more preferably from 0.8% to 9% by weight; said polymer (F) possessing reactive end groups comprising at least one of the group consisting of hydrogen atoms, oxygen atoms and ethylenically unsaturated double bonds in an amount of at least 4.5 mmol/kg, the process comprising at least the step of heat-treating the composition (C) at a temperature of at least 260 C.

The present invention relates to a phosphinated poly(2,6-dimethy phenylene oxide)oligomer, specifically an unsaturated group-containing phosphinated poly(2,6-dimethy phenylene oxide)oligomer, and processes for producing the same. A thermoset produced from the unsaturated group-containing phosphinated poly(2,6-dimethy phenylene oxide)oligomers according to the present invention exhibits flame retardancy and has a low dielectric constant and dissipation factor and a high glass transition temperature.

A process for producing a resin substrate having a hard coating layer on at least one side of a resin substrate, comprising, in the following order, a step of applying a hard coating composition containing an organopolysiloxane to at least one side of the resin substrate to form a coating film of the composition, and then applying a first heat treatment to the coating film to form a cured film; an irradiation step of applying a Xe.sub.2 excimer light irradiation treatment to the cured film in an atmosphere having an oxygen concentration of at most 5 vol %; and a step of applying an oxidation treatment to the cured film obtained by the irradiation step and then further applying a second heat treatment to form the hard coating layer.

A method for producing a poly(3-hydroxybutyrate) resin-containing composition for melt processing includes: heating a material containing a poly(3-hydroxybutyrate) resin to a temperature equal to or higher than a melting point peak temperature in differential scanning calorimetry analysis of the poly(3-hydroxybutyrate) resin and equal to or lower than a melting point peak end temperature in the differential scanning calorimetry analysis of the poly(3-hydroxybutyrate) resin, wherein the difference between the melting point peak temperature and the melting point peak end temperature of the poly(3-hydroxybutyrate) resin is 10 C. or more; and extruding the heated material to obtain a composition for melt processing that has a new crystallization peak at a temperature higher than the melting point peak temperature.

Heat treating UHMWPE by applying pressure with radial constraint at suitable times during a heating protocol reduces or eliminates cavitation, which is otherwise observed to occur when the UHMWPE is heated to a temperature above 300 C. Heat treated UHMWPE can undergo subsequent processing involving crosslinking, deformation, doping with antioxidant, and homogenizing or annealing. Heating during these steps can be carried out even above the onset melt temperature of the UHMWPE without loss of physical properties.

An aqueous biopolymer dispersion composition comprising: a biopolymer selected from the group consisting of: polybutylene adipate terephthalate (PBAT), polybutylene succinate (PBS), polybutylene succinate adipate (PBSA), polylactic acid (PLA), poly(3-hydroxybutyrate) (PHB), polycaprolactone (PCL), poly(3-hydroxybutyrate-co-3-hydroxyhexanoate) (PHBH); poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV), polyhydroxyalkanoate (PHA), and mixtures thereof; a stabilising agent selected from the group consisting of: polyvinyl alcohol, fatty alcohol ethoxylates, ethylene oxide/propylene oxide (EO/PO) block copolymers, salts of fatty acids and mixtures thereof; a rheology modifier; a cross linking agent; optional further ingredients; and water.

A method of forming a pre-cure solution for a structured organic film (SOF) is described, including contacting at least one type of segment and at least one type of pre-linker with a bio-based solvent. The method also includes dissolving the at least one type of segment and the at least one type of pre-linker within the bio-based solvent. The method also includes where the bio-based solvent has a viscosity above 0.92 MPa-s. A composition including a bio-based solvent is also disclosed.

Embodiments of the present application provides a composite film and a method for the preparation thereof, a battery module, a battery pack, and an electrical device. The method of preparing a composite film includes activating a surface of a polymer film by grafting the polymer film with a polar group on the surface, wherein the polymer film is selected from a polyolefin film or a polyethylene-vinyl acetate film; applying a slurry comprising a modified polymer resin grafted with a polar group to the activated surface of the polymer film to form a slurry coat, wherein the modified polymer resin is selected from a modified polyolefin resin grafted with a polar group or a modified polyethylene-vinyl acetate grafted with a polar group; and heating the slurry coat and the polymer film to transform the slurry coat into a modified polymer resin solid film, thereby obtaining the composite film.

The present invention relates to a method of plasticizing and densifying hydrophilic polymeric biomaterial, said hydrophilic polymeric biomaterial having at least one surface, comprising the steps of softening the surface of the hydrophilic polymeric biomaterial to be compressed; compressing the hydrophilic polymeric biomaterial by applying an elevated pressure onto the softened surface of said hydrophilic polymeric biomaterial at an elevated temperature for a predetermined period of time; decreasing the temperature and thereafter the pressure applied to the hydrophilic polymeric biomaterial; wherein a plasticizing liquid is added to said surface of the hydrophilic polymeric biomaterial to be densified, the plasticizing liquid being a non-imidazolium-based ionic liquid (IL), an organic superbase or a Deep Eutectic Solvent (DES).