Abstract: A deposition composition includes a solvent comprising a hydrofluorothioether compound represented by the following general formula (I): Rf—S—Rh where Rf is a fluorinated or perfluorinated group having 2-9 carbon atoms and optionally includes one or more catenated heteroatoms or chlorine atoms, and Rh is a non-fluorinated hydrocarbon group having 1-3 carbon atoms. The deposition composition further includes a coating material that is soluble or dispersible in said solvent.

Abstract: A compound having structural formula (II): where R2 is H, CH3, CF3, CH2CF2CF2H, or CH2CF2CF2CF2H; where R2f is a perfluoroalkyl group having 1-4 carbon atoms, optionally comprising either or both of a catenated nitrogen heteroatom and a catenated oxygen heteroatom; where R2f? is CF3 or CF2CF3; and where R2f? is CF3 or CF2CF3; with the proviso that when R2f? is CF3, then R2f? is CF3, and when R2 is H or CH3, then R2f is not CF3.

Abstract: A deposition composition includes a solvent comprising a hydrofluorothioether compound represented by the following general formula (I): Rf—S—Rh where Rf is a fluorinated or perfluorinated group having 2-9 carbon atoms and optionally includes one or more catenated heteroatoms or chlorine atoms, and Rh is a non-fluorinated hydrocarbon group having 1-3 carbon atoms. The deposition composition further includes a coating material that is soluble or dispersible in said solvent.

Abstract: A composition includes a compound having structural formula (I): Rf—S—Rh (I) wherein (i) Rf is a partially fluorinated or perfluorinated group having 2 to 6 carbon atoms and optionally comprises one or more catenated heteroatoms, and (ii) Rh is a non-fluorinated hydrocarbon group having 1-3 carbon atoms and optionally comprises one or more catenated heteroatoms. The composition further includes an organic lubricant contaminant.

Abstract: A process for removing an electroluminescent material from a substrate. The process includes providing a substrate having an electroluminescent material disposed on a surface thereof. The process further includes contacting the substrate with a composition. The composition includes a hydroflourocompound an organic solvent that forms an azeotrope with the hydroflourocompound when mixed with the hydroflourocompound.

Abstract: Synthesizing an alkyl-caprolactone includes hydrogenating an alkyl-phenol to yield a first mixture comprising an alkyl-cyclohexanone and an alkyl-cyclohexanol; separating the alkyl-cyclohexanone from the first mixture to yield a first portion of a purified alkyl-cyclohexanone; oxidizing the first portion of the purified alkyl-cyclohexanone to yield a second mixture comprising an alkyl-caprolactone, the alkyl-cyclohexanone, and the alkyl-cyclohexanol; separating the alkyl-caprolactone from the second mixture to yield a third mixture comprising the alkyl-cyclohexanone and the alkyl-cyclohexanol; combining the third mixture and the first mixture in to yield a fourth mixture; separating the alkyl-cyclohexanone from the fourth mixture to yield a second portion of the purified alkyl-cyclohexanone; oxidizing the second portion of the purified alkyl-cyclohexanone to yield a fifth mixture comprising the alkyl-caprolactone, the alkyl-cyclohexanone, and the alkyl-cyclohexanol; separating the alkyl-caprolactone from the

Abstract: Synthesizing an alkyl-caprolactone includes hydrogenating an alkyl-phenol to yield a first mixture comprising an alkyl-cyclohexanone and an alkyl-cyclohexanol; separating the alkyl-cyclohexanone from the first mixture to yield a first portion of a purified alkyl-cyclohexanone; oxidizing the first portion of the purified alkyl-cyclohexanone to yield a second mixture comprising an alkyl-caprolactone, the alkyl-cyclohexanone, and the alkyl-cyclohexanol; separating the alkyl-caprolactone from the second mixture to yield a third mixture comprising the alkyl-cyclohexanone and the alkyl-cyclohexanol; combining the third mixture and the first mixture in to yield a fourth mixture; separating the alkyl-cyclohexanone from the fourth mixture to yield a second portion of the purified alkyl-cyclohexanone; oxidizing the second portion of the purified alkyl-cyclohexanone to yield a fifth mixture comprising the alkyl-caprolactone, the alkyl-cyclohexanone, and the alkyl-cyclohexanol; separating the alkyl-caprolactone from the

Abstract: A method for producing a magnetic recording medium while minimizing electrostatic charge buildup on the medium during production. The method comprises applying a liquid material over a surface of a moving web to form a continuous wet coating thereon and smoothing the wet coating with a flexible blade having two major surfaces. The flexible smoothing blade comprises a conductive layer and is positioned so that a portion of one major surface is in contact with the wet coating so that electrostatic charge on the coated web is continuously dissipated.

Abstract: A method of depositing a magnetic recording media coating onto a substrate, wherein the coating is substantially free of Benard Cells, the method comprising the steps of: (a) providing a dispersion comprising a polymeric binder, a pigment, and a solvent; (b) coating the dispersion onto a surface of the substrate; (c) drying the dispersion; (d) calculating values comprising .mu., .beta., and d representing the viscosity, temperature gradient, and wet caliper of the dispersion, respectively; and (e) during the course of carrying out steps (a), (b), and (c), maintaining the ratio ##EQU1## below a threshold value sufficient to substantially prevent the formation of Benard Cells in the magnetic recording media coating.