The present disclosure provides a composition containing a compound represented by General Formula (1) and a polymer compound, in which a content of a chloride ion is less than 1.5 ppm with respect to a total mass of the composition, and provides a compound.

##STR00001##

In General Formula (1), Het.sup.1 represents a divalent aromatic heterocyclic residue of a 5-membered ring or a 6-membered ring, X.sup.a, X.sup.b, X.sup.c, and X.sup.d each independently represent a heteroatom, Y.sup.a, Y.sup.b, Y.sup.c, Y.sup.d, Y.sup.e and Y.sup.f each independently represent a heteroatom or a carbon atom, and two 6-membered rings bonded to Het.sup.1 each independently may have a double bond.

A resist underlayer composition including a polymer including a main chain, a side chain, or a main chain and a side chain including a heterocycle including two or more nitrogen atoms in the ring of the heterocycle, a compound including a moiety represented by Chemical Formula 1, and a solvent is provided. A method of forming patterns using the resist underlayer composition is also provided

##STR00001##

A resist underlayer composition including a polymer including a main chain, a side chain, or a main chain and a side chain including a heterocycle including two or more nitrogen atoms in the ring of the heterocycle, a compound including a moiety represented by Chemical Formula 1, and a solvent is provided. A method of forming patterns using the resist underlayer composition is also provided

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Various aspects relate to binder compositions including a bio-based component and pre-blends for forming the same. A binder composition includes an oligomerized biorenewable oil that is at least 10 wt % of the binder composition. The binder composition also includes an Asphaltene Additive comprising at least 20 wt % to 100 wt % asphaltenes, wherein the Asphaltene Additive is at least 8 wt % of the binder composition.

Various aspects relate to binder compositions including a bio-based component and pre-blends for forming the same. A binder composition includes an oligomerized biorenewable oil that is at least 10 wt % of the binder composition. The binder composition also includes an Asphaltene Additive comprising at least 20 wt % to 100 wt % asphaltenes, wherein the Asphaltene Additive is at least 8 wt % of the binder composition.

A polyvinyl chloride-asphaltene composite and a method of making the polyvinyl chloride-asphaltene composite is disclosed. The composite includes a polyvinyl chloride (PVC) polymer in an amount of 90 to 99.5 wt. %, based on a total weight of the polyvinyl chloride-asphaltene composite, and a filler in an amount of 10 wt. % or less, based on a total weight of the polyvinyl chloride-asphaltene composite. The filler is an asphaltene, the asphaltene is the only filler present, and the asphaltene is uniformly dispersed within a matrix of the PVC polymer. The polyvinyl chloride-asphaltene composite of the present disclosure demonstrates enhanced thermal stability and improved mechanical tensile or thermo-mechanical properties.

A polyvinyl chloride-asphaltene composite and a method of making the polyvinyl chloride-asphaltene composite is disclosed. The composite includes a polyvinyl chloride (PVC) polymer in an amount of 90 to 99.5 wt. %, based on a total weight of the polyvinyl chloride-asphaltene composite, and a filler in an amount of 10 wt. % or less, based on a total weight of the polyvinyl chloride-asphaltene composite. The filler is an asphaltene, the asphaltene is the only filler present, and the asphaltene is uniformly dispersed within a matrix of the PVC polymer. The polyvinyl chloride-asphaltene composite of the present disclosure demonstrates enhanced thermal stability and improved mechanical tensile or thermo-mechanical properties.

Described are polymerizable high energy light absorbing compounds. The compounds absorb various wavelengths of ultraviolet and/or high energy visible light and are suitable for incorporation in various products, such as biomedical devices and ophthalmic devices. Such devices exhibit a number of desirable properties, including favorable vision break-up times.

Described are polymerizable high energy light absorbing compounds. The compounds absorb various wavelengths of ultraviolet and/or high energy visible light and are suitable for incorporation in various products, such as biomedical devices and ophthalmic devices.

Described are polymerizable high energy light absorbing compounds. The compounds absorb various wavelengths of ultraviolet and/or high energy visible light and are suitable for incorporation in various products, such as biomedical devices and ophthalmic devices. Such devices exhibit a number of desirable properties, including favorable rates of pervaporation.