Abstract: Polyolefins incorporating hindered phenol groups covalently bound thereto are disclosed. The hindered phenols are covalently bound to the polyolefin through a residue of an alkenyl compound having a carboxylic acid and/or anhydride on the polyolefin. Such polyolefins can be prepared by reacting the following components together under heat: (a) a polyolefin; (b) an alkenyl compound having a carboxylic acid and/or anhydride; and (c) a hindered phenol reagent that can react with the carboxylic acid and/or anhydride of the alkenyl compound; to produce a polyolefin having hindered phenol groups covalently bound thereto. Reactive compounding of such components allows preparation of such polyolefins in a continuous process and in a single reaction step.

Abstract: A poroelastic biomaterial including a polyaryletherketone (PAEK) matrix polymer and a plurality of tortuous channels extending from one surface to another surface of the biomaterial is disclosed. Advantageously, the poroelastic biomaterial can have a porosity from about 5% to about 40% and high mechanical properties. The poroelastic biomaterials can be fabricated into orthopedic implant devices and can be used as a tissue scaffolds.

Abstract: Polyolefins incorporating hindered phenol groups covalently bound thereto are disclosed. The hindered phenols are covalently bound to the polyolefin through a residue of an alkenyl compound having a carboxylic acid and/or anhydride on the polyolefin. Such polyolefins can be prepared by reacting the following components together under heat: (a) a polyolefin; (b) an alkenyl compound having a carboxylic acid and/or anhydride; and (c) a hindered phenol reagent that can react with the carboxylic acid and/or anhydride of the alkenyl compound; to produce a polyolefin having hindered phenol groups covalently bound thereto. Reactive compounding of such components allows preparation of such polyolefins in a continuous process and in a single reaction step.

Abstract: A poroelastic biomaterial having a polyaryletherketone (PAEK) matrix polymer with a plurality of channels and/or pores can include thereon or within an active agent, e.g., an agent that promotes osseointegration of the biomaterial, on surfaces thereof. Advantageously, the PAEK matrix polymer can have a plurality of tortuous channels extending from one surface to another surface of the matrix. The poroelastic biomaterials can be fabricated into orthopedic implant parts or devices, and can be used as a tissue scaffolds.

Abstract: Polyolefins having the same or different functional groups covalently bound to the polyolefin, such as polyolefins having hindered phenol groups bound thereto, can be prepared by from a maleic anhydride modified polyolefin, with or without a coupling agent, and a hindered phenol reagent under heat, e.g., by heating the components to at least about 170° C., such as by reactive extrusion. A polyolefin having hindered phenol groups can be added to the components as a stabilizer prior to or during reacting the components together under heat.

Abstract: Polyolefins incorporating hindered phenol groups covalently bound thereto are disclosed. The hindered phenols are covalently bound to the polyolefin through a residue of an alkenyl compound having a carboxylic acid and/or anhydride on the polyolefin. Such polyolefins can be prepared by reacting the following components together under heat: (a) a polyolefin; (b) an alkenyl compound having a carboxylic acid and/or anhydride; and (c) a hindered phenol reagent that can react with the carboxylic acid and/or anhydride of the alkenyl compound; to produce a polyolefin having hindered phenol groups covalently bound thereto. Reactive compounding of such components allows preparation of such polyolefins in a continuous process and in a single reaction step.

Abstract: Polyolefins having the same or different functional groups covalently bound to the polyolefin, such as polyolefins having hindered phenol groups bound thereto, can be prepared by from a maleic anhydride modified polyolefin, with or without a coupling agent, and a hindered phenol reagent under heat, e.g., by heating the components to at least about 170° C., such as by reactive extrusion. A polyolefin having hindered phenol groups can be added to the components as a stabilizer prior to or during reacting the components together under heat.

Abstract: Polyolefins having the same or different functional groups covalently bound to the polyolefin, such as polyolefins having hindered phenol groups bound thereto, can be prepared by from a maleic anhydride modified polyolefin, with or without a coupling agent, and a hindered phenol reagent under heat, e.g., by heating the components to at least about 170° C., such as by reactive extrusion. A polyolefin having hindered phenol groups can be added to the components as a stabilizer prior to or during reacting the components together under heat.

Abstract: A poroelastic biomaterial including a polyaryletherketone (PAEK) matrix polymer and a plurality of tortuous channels extending from one surface to another surface of the biomaterial is disclosed. Advantageously, the poroelastic biomaterial can have a porosity from about 5% to about 40% and high mechanical properties. The poroelastic biomaterials can be fabricated into orthopedic implant devices and can be used as a tissue scaffolds.

Abstract: Polyolefins having the same or different functional groups covalently bound to the polyolefin, such as polyolefins having hindered phenol groups bound thereto, can be prepared by from a maleic anhydride modified polyolefin, with or without a coupling agent, and a hindered phenol reagent under heat, e.g., by heating the components to at least about 170° C., such as by reactive extrusion. A polyolefin having hindered phenol groups can be added to the components as a stabilizer prior to or during reacting the components together under heat.

Abstract: Polymer blends having improved electromechanical responses and mechanical properties for use in electromechanical application are disclosed. In particular, polymer blend including at least one electrostrictive terpolymer, e.g., poly(vinylidene fluoride-trifluoroethylene-chlorofluoroethylene) (P(VDF-TrFE-CFE)) or a derivative thereof, and at least one fluoropolymer, e.g., PVDF or derivative thereof such as PVD-TrFE are disclosed. The polymer blends advantageously have a transverse strain, i.e., a strain perpendicular to the applied electric field direction, that is about 1.5% or higher (as measured at 100 MV/m) while also having an elastic modulus of no less than about 400 MPa (as measured at 30° C. and 1 Hz by dynamic mechanical analyzer).

Abstract: Polymer blends having improved electromechanical responses and mechanical properties for use in electromechanical application are disclosed. In particular, polymer blend including at least one electrostrictive terpolymer, e.g., poly(vinylidene fluoride-trifluoroethylene-chlorofluoroethylene) (P(VDF-TrFE-CFE)) or a derivative thereof, and at least one fluoropolymer, e.g., PVDF or derivative thereof such as PVD-TrFE are disclosed. The polymer blends advantageously have a transverse strain, i.e., a strain perpendicular to the applied electric field direction, that is about 1.5% or higher (as measured at 100 MV/m) while also having an elastic modulus of no less than about 400 MPa (as measured at 30° C. and 1 Hz by dynamic mechanical analyzer).

Abstract: A multilayer film useful for capacitive applications comprises a high energy density layer and a dielectric blocking layer. In some embodiments, a conducting film is located between the high energy density layer and the blocking layer. The high energy density layer may be a fluoropolymer, such as a polymer or copolymer of poly-1,1-difluoroethene or a derivative thereof. The multilayer film may have high energy density (for example,. >8 J/cm3) and low dielectric loss, for example less than 2%, and preferably less than 1%.

Abstract: A process for the facile two-step synthesis of methanol from methane is disclosed. In accordance with the invention, an appropriate combination of initiator and reaction medium is employed to achieve methane conversion in very high selectivity and yield under near-ambient temperature.

Abstract: A process for the facile two-step synthesis of methanol from methane is disclosed. In accordance with the invention, an appropriate combination of initiator and reaction medium is employed to achieve methane conversion in very high selectivity and yield under near-ambient temperature.

Abstract: A process for direct oxidative carbonylation of lower alkanes to acids having one greater carbon atom. The process uses a metal salt catalyst promoted by halide ions and/or a metal with oxygen as the oxidant in an aqueous medium. The process is especially effective for conversion of methane to acetic acid.

Abstract: A process for catalytic direct oxidation of hydrocarbons, particularly lower alkanes and single ring aromatics, to acids by dioxygen under mild temperature conditions using specified metal or metal salt catalysts. Turnovers in excess of 1000 for acetic acid formation from ethane and in excess of 100 for formic acid formation from methane have been obtained at reaction temperatures below about 100.degree. C. using palladium catalyst. A coreductant of carbon monoxide in an aqueous system is preferred.