In one or more embodiments, the present invention provides am method of making a poly(propylene fumarate-co-succinate) (PPFS) copolymer containing a random incorporation of succinate groups and targetable reduction profiles without the need for three or more monomer units. To achieve this, a time-dependent sonication-promoted zinc/acetic acid reduction of the PPM unsaturated double bonds has been used to create a random PPMS copolymer which may be isomerized into the PPFS equivalent. By changing the sonication time as well as the ratios of acetic acid, zinc, and PPM unsaturated alkenes, partial reduction of the PPM alkenes has been shown to give PPMS products containing varying compositions of succinic and maleate units, which may then be isomerized to the PPFS product.

This invention relates to a new polyester which is particularly suitable for use in the manufacture of mass-produced articles characterised by excellent mechanical properties, in particular high tensile strength and tensile modulus, associated with a high barrier property against oxygen and carbon dioxide.

This invention relates to a new polyester which is particularly suitable for use in the manufacture of mass-produced articles characterised by excellent mechanical properties, in particular high tensile strength and tensile modulus, associated with a high barrier property against oxygen and carbon dioxide.

The present invention relates to a method for producing a mixture comprising at least one compound having at least two hydroxy and/or amino groups made of a biomass material. The invention also relates to such a mixture and to the use thereof for producing a polymer such as for example a polyurethane foam.

The present invention relates to a method for producing a mixture comprising at least one compound having at least two hydroxy and/or amino groups made of a biomass material. The invention also relates to such a mixture and to the use thereof for producing a polymer such as for example a polyurethane foam.

The present invention provides an asphalt modifier composed of a crystalline polyester that has a structural unit derived from an alcohol component containing a linear aliphatic alcohol and a structural unit derived from a carboxylic acid component, the crystalline polyester having a melting point of 65° C. or higher and 160° C. or lower.

A method for preparing a biodegradable polyester elastomer includes a following steps comprising: dissolving a predetermined amount of titanium dioxide in an aqueous mixture of sulphuric acid, DI water, and ethanol to form a first solution; refluxing the first solution in a silicone oil bath and a stirring speed of 300-450 rpm at a temperature of 90-100° C. to form a second solution; preparing a solid superacid catalyst by drying, grinding and calcining sulfated titania and using this catalyst to produce a biodegradable polyester elastomer.

A method for preparing a biodegradable polyester elastomer includes a following steps comprising: dissolving a predetermined amount of titanium dioxide in an aqueous mixture of sulphuric acid, DI water, and ethanol to form a first solution; refluxing the first solution in a silicone oil bath and a stirring speed of 300-450 rpm at a temperature of 90-100° C. to form a second solution; preparing a solid superacid catalyst by drying, grinding and calcining sulfated titania and using this catalyst to produce a biodegradable polyester elastomer.

Polymer-based electrolyte materials that may be used as proton exchange membranes in proton exchange membrane fuel cells are described. The disclosed polymer electrolyte materials can be generally defined by a general 1,3-dicarbonyl repeat unit that may include various side chain and main chain constituents changing the acidity of the C—H proton(s) located between the carbonyl groups. Accordingly, by varying such side-chain and main-chain constituents, the proton-conduction properties the disclosed proton exchange membranes can be manipulated, and methods of producing the same. Methods of producing such polymer electrolyte materials are also disclosed.

An alkyd polymer composition for fast-drying, low VOC applications is provided. The alkyd polymer incorporates a minimum required level of a cyclic ether- and hydroxyl-containing composition formed from a sugar alcohol during the alcoholysis step while synthesizing the alkyd polymer. The disclosure also relates to the cyclic ether- and hydroxyl-containing composition which must have a minimum required level of cyclic ether structure incorporated therein in order to produce a sufficiently fast-drying alkyd polymer. Methods of making the cyclic ether- and hydroxyl-containing composition and the alkyd polymer comprising, as polymerized units, the cyclic ether- and hydroxyl-containing composition and a poly acid and/or an anhydride compound, as well as an optional polyol, other than the sugar alcohol, are also provided. Also provided is a 13 C NMR method of characterizing the necessary minimum required level of cyclic ether ring structure in the cyclic ether- and hydroxyl-containing composition and the alkyd polymer formed therefrom.