G03G9/09335

Electrostatic printing of cyclodextrin compositions

Disclosed herein are methods of electrostatically printing a cyclodextrin composition on a substrate, the method including forming an electrostatically printable composition comprising a polymer and one or more cyclodextrins, one or more cyclodextrin inclusion complexes, or a combination thereof, and electrostatically printing the composition on a substrate. Also described are electrostatically printable compositions, methods of making the compositions, printing systems employing the compositions, substrates having the composition electrostatically printed thereon, laminates thereof, and uses of the printed substrates and laminates.

Electrostatic printing of cyclodextrin compositions

Disclosed herein are methods of electrostatically printing a cyclodextrin composition on a substrate, the method including forming an electrostatically printable composition comprising a polymer and one or more cyclodextrins, one or more cyclodextrin inclusion complexes, or a combination thereof, and electrostatically printing the composition on a substrate. Also described are electrostatically printable compositions, methods of making the compositions, printing systems employing the compositions, substrates having the composition electrostatically printed thereon, laminates thereof, and uses of the printed substrates and laminates.

TONER
20190187579 · 2019-06-20 · ·

A toner includes toner particles. The toner particles each include a composite core and a shell layer covering a surface of the composite core. The composite core is a composite of a toner core and organic particles located on a surface of the toner core. The toner core contains a releasing agent having a carboxyl group. The organic particles contain a resin having a carboxyl group and a mass average molecular weight of from 30,000 to 50,500. The shell layer includes a unit having a non-ring-opened oxazoline group. An amount of the non-ring-opened oxazoline group contained in 1 g of the toner as measured by gas chromatography-mass spectrometry is from 500 mol to 1,400 mol. An endothermic quantity due to melting of the releasing agent contained in 1 mg of the toner as measured by differential scanning calorimetry is from 80 mJ to 160 mJ.

Electrostatic Printing of Cyclodextrin Compositions
20240252448 · 2024-08-01 ·

Disclosed herein are methods of electrostatically printing a cyclodextrin composition on a substrate, the method including forming an electrostatically printable composition comprising a polymer and one or more cyclodextrins, one or more cyclodextrin inclusion complexes, or a combination thereof, and electrostatically printing the composition on a substrate. Also described are electrostatically printable compositions, methods of making the compositions, printing systems employing the compositions, substrates having the composition electrostatically printed thereon, laminates thereof, and uses of the printed substrates and laminates.

MAGNETIC TONER
20190025723 · 2019-01-24 · ·

A magnetic toner includes toner particles. The toner particles each include a toner core and a shell layer covering a surface of the toner core. The toner cores contain a polyester resin and a magnetic powder. The magnetic powder includes specific magnetic particles. The shell layers contain a specific vinyl resin.

Toner formulation having a silane surface treated on its outer surface and method of preparing the same

A chemically prepared toner composition according to one example embodiment includes a core including a first polymer binder, a colorant and a release agent; a shell that is formed around the core that includes a second polymer binder; and a borax coupling agent between the core and the shell and an alkoxysilane hydrocarbon or combination of different alkoxysilane hydrocarbons that are bonded to the outer surface of the shell using a hydrolytic deposition process. This successful alkoxysilane hydrocarbon surface treatment on the outer surface of the toner particle results in attaining a desirable charge stability in hot and humid environments and ultimately improving the quality of the toner, especially by reducing toner dusting, toner fuming and ultra-fine particles generation.

Toner formulation having a silane surface treated on its outer surface and method of preparing the same

A method for producing core shell toner for electrophotography according to one embodiment, includes surface treating the outer surface of a core shell toner particle with a alkoxysilane hydrocarbon or combination of different alkoxysilane hydrocarbons using a hydrolytic deposition process after the core shell toner particle is fully formed. This method results in the bonding of the alkoxysilane hydrocarbon or combination of different alkoxysilane hydrocarbons to the outer surface of the core shell toner particle. In an alternative method, the outer surface of the toner is surface treated with the alkoxysilane hydrocarbon solution and then fused to form toner particles. The alkoxysilane hydrocarbon surface treated core shell toner also can be mixed with magnetic carrier beads to form a developer mix to be used in a dual component development electrophotographic printer.

TONER

Provided is a toner, including a toner particle having: a toner base particle containing a binder resin and a colorant; and protrusion derived from a resin fine particle in a surface of the toner base particle, wherein the protrusion is covered with a condensation product of an organosilicon compound represented by the formula (1), and wherein the resin fine particle is in direct contact with the toner base particle.


(R.sup.a).sub.nSi(R.sup.b).sub.4-n(1)

TONER

Provided is a toner comprising a toner particle including a toner base particle and fine particles present on a surface of the toner base particle, wherein each of the fine particles includes a core fine particle and a condensate of at least one organosilicon compound selected from the group consisting of organosilicon compounds represented by specific structural formulas, the condensate coating the surface of the core fine particle, and in a wettability test of the toner with respect to a methanol/water mixed solvent, a methanol concentration, when a transmittance of light having a wavelength of 780 nm is 50%, is 5.0 to 20.0% by volume:

##STR00001## in above Formulas, each of R.sup.a, R.sup.b and R.sup.c independently represents an alkyl group, an alkenyl group, an acetoxy group, an acyl group, an aryl group, or a methacryloxyalkyl group, R.sup.1 to R.sup.5 each independently represents a halogen atom or an alkoxy group.

Hybrid toner compositions

A hybrid toner composition including a first wax; a second wax that is different from the first wax; wherein the first wax comprises a paraffin wax having a peak melting point of from about 60 to about 80 C.; wherein the second wax comprises an ester wax having a peak melting point of from about 60 to about 80 C.; a first resin comprising an amorphous polyester resin and at second resin comprising at least one of a styrene, an acrylate, or a combination thereof; and an optional colorant.