Abstract: In one aspect, inks for use with a three-dimensional (3D) printing system are described herein. In some embodiments, an ink described herein comprises 10-70 wt. % cyclopolymerizable monomer, based on the total weight of the ink. The cyclopolymerizable monomer comprises a first ethenyl or ethynyl moiety and a second ethenyl or ethynyl moiety. Additionally, the ?-carbon of the first ethenyl or ethynyl moiety and the ?-carbon of the second ethenyl or ethynyl moiety have a 1,5-, 1,6-, 1,7-, or 1,8-relationship.

Abstract: Phase change ink compositions having a phase change carrier composition containing a wax and a wax-soluble near-infrared (NIR) dye having an absorption maximum in the wavelength region from about 700 nm to about 1400 nm. Near-infrared prints prepared with such phase change ink compositions. Methods of producing a layer of such a phase change ink on the surface of a substrate.

Abstract: A phase change ink composition comprising an amorphous component, a crystalline material, and optionally, a colorant, which are suitable for ink jet printing, including printing on coated paper substrates and are suitable for fast printing processes. In particular, the crystalline component comprises a diurethane compound or derivatives thereof.

Abstract: An embodiment of the present disclosure is directed to an amorphous bis-urea compound having a formula 1: where X is a branched alkyl bridge and R? and R? are alkyl groups.

Abstract: A compound comprising a boron subphthalocyanine moiety, a plurality of solubilizing substituents positioned on peripheral cyclic groups of the boron subphthalocyanine moiety and an axial substituent positioned on the boron atom of the boron subphthalocyanine moiety. The plurality of solubilizing substituents comprise an oxygen or sulfur containing functional group and a substituted or unsubstituted, linear, branched or cyclic, aliphatic or aromatic terminal hydrocarbyl group that is 8 or more carbon atoms in length, the hydrocarbyl group optionally containing one or more heteroatoms. The axial substituent is selected from the group consisting of halogen, alkyloxy, haloalkyloxy, ester, carbonyl substituted alkyl, carbonyl substituted haloalkyl, alkylaryloxy, haloalkylaryloxy, alkyl sulfonyl, haloalkyl sulfonyl, alkylaryl sulfonyl and haloalkylaryl sulfonyl.

Abstract: A dye compound of formula 1: where R and R? are substituents independently selected from the group consisting of a hydrogen atom, C1 to C4 alkyl and a solubilizing moiety comprising a substituted or unsubstituted C10 to C70 hydrocarbyl group. At least one of R and R? is not a hydrogen atom or C1 to C4 alkyl. R? and R?? can be independently selected from the group consisting of a hydrogen atom, C1 to C6 alkyl groups or halogens; and X is a squaric acid moiety. A property of the dye compound is that it absorbs radiation having a wavelength in the range of about 700 nm to about 1400 nm.

Abstract: An embodiment of the present disclosure is directed to an amorphous bis-urea compound having a formula 1: where X is a branched alkyl bridge and R? and R? are alkyl groups.

Abstract: A compound comprising a boron subphthalocyanine moiety, a plurality of solubilizing substituents positioned on peripheral cyclic groups of the boron subphthalocyanine moiety and an axial substituent positioned on the boron atom. The plurality of solubilizing substituents comprise an oxygen or sulfur containing functional group and a substituted or unsubstituted, linear, branched or cyclic, aliphatic or aromatic terminal hydrocarbyl group that is 8 or more carbon atoms in length, the hydrocarbyl group optionally containing one or more heteroatoms. The axial substituent is a cyclic group selected from the group consisting of heterocyclic amine groups, diaryl ketone groups, benzotriazole groups, benzyl alcohol groups and polycyclic aromatic hydrocarbon groups, the cyclic group being bonded to the boron atom by an oxygen containing linking moiety, the cyclic group optionally being substituted with one or more additional substituents.

Abstract: A phase change ink composition including an ink vehicle; an optional colorant; and ethylene vinyl acetate in an amount of from about 0.1 to about 10 percent by weight based on the total weight of the phase change ink composition.

Abstract: A compound comprising a boron subphthalocyanine moiety, a plurality of solubilizing substituents positioned on peripheral cyclic groups of the boron subphthalocyanine moiety and an axial substituent positioned on the boron atom. The plurality of solubilizing substituents comprise an oxygen or sulfur containing functional group and a substituted or unsubstituted, linear, branched or cyclic, aliphatic or aromatic terminal hydrocarbyl group that is 8 or more carbon atoms in length, the hydrocarbyl group optionally containing one or more heteroatoms. The axial substituent is a cyclic group selected from the group consisting of heterocyclic amine groups, diaryl ketone groups, benzotriazole groups, benzyl alcohol groups and polycyclic aromatic hydrocarbon groups, the cyclic group being bonded to the boron atom by an oxygen containing linking moiety, the cyclic group optionally being substituted with one or more additional substituents.

Abstract: A compound comprising a boron subphthalocyanine moiety, a plurality of solubilizing substituents positioned on peripheral cyclic groups of the boron subphthalocyanine moiety and an axial substituent positioned on the boron atom of the boron subphthalocyanine moiety. The plurality of solubilizing substituents comprise an oxygen or sulfur containing functional group and a substituted or unsubstituted, linear, branched or cyclic, aliphatic or aromatic terminal hydrocarbyl group that is 8 or more carbon atoms in length, the hydrocarbyl group optionally containing one or more heteroatoms. The axial substituent is selected from the group consisting of halogen, alkyloxy, haloalkyloxy, ester, carbonyl substituted alkyl, carbonyl substituted haloalkyl, alkylaryloxy, haloalkylaryloxy, alkyl sulfonyl, haloalkyl sulfonyl, alkylaryl sulfonyl and haloalkylaryl sulfonyl.

Abstract: Phase change ink compositions having a phase change carrier composition containing a wax and a wax-soluble near-infrared (NIR) dye having an absorption maximum in the wavelength region from about 700 nm to about 1400 nm. Near-infrared prints prepared with such phase change ink compositions. Methods of producing a layer of such a phase change ink on the surface of a substrate.

Abstract: A dye compound of formula 1: where R and R? are substituents independently selected from the group consisting of a hydrogen atom, C1 to C4 alkyl and a solubilizing moiety comprising a substituted or unsubstituted C10 to C70 hydrocarbyl group. At least one of R and R? is not a hydrogen atom or C1 to C4 alkyl. R? and R?? can be independently selected from the group consisting of a hydrogen atom, C1 to C6 alkyl groups or halogens; and X is a squaric acid moiety. A property of the dye compound is that it absorbs radiation having a wavelength in the range of about 700 nm to about 1400 nm.

Abstract: A phase change ink composition comprising an amorphous component, a crystalline material, and optionally, a colorant, which are suitable for high speed ink jet printing, including printing on coated paper substrates. In embodiments, the amorphous component comprises a diurethane compound or derivatives thereof.

Abstract: Disclosed herein are curable solid inks which are solid at room temperature and molten at an elevated temperature at which the molten ink is applied to a substrate. In particular, the curable solid inks of the present embodiments comprise low molecular weight amide gellants that impart self-leveling capabilities to the inks. Also disclosed herein are methods for making the amide gellant and the inks comprising the amide gellants.

Abstract: A perimidine coupler of formula 1: where R and R? are substituents independently selected from the group consisting of a hydrogen atom, C1 to C4 alkyl or a solubilizing moiety comprising a substituted or unsubstituted C10 to C70 hydrocarbyl group. At least one of R and R? is not a hydrogen atom or C1 to C4 alkyl. R? and R?? can be independently selected from the group consisting of a hydrogen atom, C1 to C6 alkyl groups and halogens.

Abstract: Exemplary embodiments provide a phase change ink composition including at least a first semi-crystalline material having a high amorphous content; and at least a second semi-crystalline material having a high crystalline content, such that the phase change ink has a viscosity ranging from about 0.1 cps to about 15 cps at a temperature ranging from about 60° C. to about 145° C. and the phase change ink composition has excellent robustness when forming images or printing on a printing substrate.

Abstract: A solid ink composition comprising an amorphous component, a crystalline material, and optionally, a colorant, which are suitable for ink jet printing, including printing on coated paper substrates. In embodiments, the solid ink formulation comprises a blend of amorphous and crystalline components which provides a solid ink with excellent rheological properties and robustness when forming images or printing on coated paper substrates.

Abstract: A phase change ink composition including an ink vehicle; an optional colorant; and ethylene vinyl acetate in an amount of from about 0.1 to about 10 percent by weight based on the total weight of the phase change ink composition.

Abstract: Exemplary embodiments provide a phase change ink composition including at least a first semi-crystalline material having a high amorphous content; and at least a second semi-crystalline material having a high crystalline content, such that the phase change ink has a viscosity ranging from about 0.1 cps to about 15 cps at a temperature ranging from about 60° C. to about 145° C. and the phase change ink composition has excellent robustness when forming images or printing on a printing substrate.