Abstract: Fibrous structures, for example sanitary tissue products, such as toilet tissue, having one or more neat surfactant components on at least one exterior surface, methods for making same, and methods for removing fecal matter from a user's skin are provided.

Abstract: Fibrous structures, for example sanitary tissue products, such as toilet tissue, having one or more neat surfactant components on at least one exterior surface, methods for making same, and methods for removing fecal matter from a user's skin are provided.

Abstract: The present invention relates to a fibrous structure including one or more encapsulated malodor reduction compositions and methods of making and using such a fibrous structure.

Abstract: Fibrous structures, for example sanitary tissue products, such as toilet tissue, having one or more neat surfactant components on at least one exterior surface, methods for making same, and methods for removing fecal matter from a user's skin are provided.

Abstract: The present invention relates to a fibrous structure including one or more encapsulated malodor reduction compositions and methods of making and using such a fibrous structure.

Abstract: The present invention relates to a fibrous structure including one or more malodor reduction compositions and methods of making and using such a fibrous structure.

Abstract: Fibrous structures, for example sanitary tissue products, such as toilet tissue, having one or more neat, endothermic phase change materials on at least one exterior surface, methods for making same, and methods for eliciting a sensation on a user's skin are provided.

Abstract: Fibrous structures, for example sanitary tissue products, such as toilet tissue, containing one or more sensates, more particularly one or more TRPM8 receptor triggering agents, a sensate composition, for example surface softening composition, comprising one or more TRPM8 receptor triggering agents, and methods for making same are provided.

Abstract: A method for demonstrating the comparative break-though strengths of at least two tissue products is disclosed. The steps include: a) providing a break-through test apparatus b) providing the tissue products; c) observing a first condition of each tissue product; d) disposing a first of the tissue products between a lower platen and an upper platen in a face-to-face-to-face relationship between coextensive apertures disposed within the lower and upper platen; e) providing a simulated mucous composition; f) directing a first portion of the simulated mucous composition toward the first tissue product; g) observing a second condition of the first tissue product; h) disposing a second tissue product between the coextensive apertures; i) directing a second portion of the simulated mucous composition toward the second tissue product; j) observing a second condition of the second tissue product; and, k) comparing the second condition of the first tissue product and the second condition of the second tissue product.

Abstract: A multi-ply paper product is disclosed. The multi-ply paper product is provided with a first play and a second ply. The first ply is a lotioned fibrous structure having a wet burst of less than about 100 grams. The second ply is a non-lotioned fibrous structure having a wet burst of greater than about 100 grams.

Abstract: The present disclosure provides a paper product having at least two plies. Only one outer surface of the tissue paper product has a lotion and a polyhydroxy compound having a molecular weight ranging from about 150 to about 4,000 and selected from the group consisting of glycerols, polyglycerols, polyethylene glycols (PEGs), polyoxyethylenes, polyoxypropylenes, and combinations thereof applied thereto by slot extrusion. The polyhydroxy compound provides the tissue paper product with a Wet Burst greater than about 90 g, a Dynamic Coefficient of Friction less than about 0.9, and a Bending Flexibility less than about 0.042 gf cm2/cm.

Abstract: An apparatus for testing the break-through strength of a tissue product is disclosed. The apparatus comprises a dose addition assembly having an opening and a sample holder. The sample holder comprises a lower platen and an upper platen disposed in a fact to face relationship and each having coextensive openings disposed therein. The opening of the dose addition assembly is disposed proximate to one of the openings disposed within the upper and lower platens. A substance is disposed within the dose addition assembly and is capable of being expectorated from the opening of the dose addition assembly through one of the openings disposed within the upper and lower platens onto a tissue product disposed between the upper and lower platens and within the openings disposed within the upper and lower platens.

Abstract: A method for testing the break-through strength of a tissue product is disclosed. The method entails the steps of: a) observing a first condition of the tissue product; b) disposing the tissue product between a lower platen and an upper platen; c) disposing at least a portion of the tissue product within an aperture disposed within the lower platen and an aperture disposed within the upper platen; d) providing a simulated mucous composition; e) directing the simulated mucous composition toward the tissue product disposed within the aperture disposed within the lower platen and the aperture disposed within the upper platen; f) after step d), observing a second condition of the tissue product; and, g) comparing the first and the second conditions of the tissue product.

Abstract: The present disclosure provides a paper product having at least two plies. Only one outer surface of the tissue paper product has a lotion and a polyhydroxy compound having a molecular weight ranging from about 150 to about 4,000 and selected from the group consisting of glycerols, polyglycerols, polyethylene glycols (PEGs), polyoxyethylenes, polyoxypropylenes, and combinations thereof applied thereto by slot extrusion. The polyhydroxy compound provides the tissue paper product with a Wet Burst greater than about 90 g, a Dynamic Coefficient of Friction less than about 0.9, and a Bending Flexibility less than about 0.042 gf cm2/cm.

Abstract: A tissue paper product having at least one ply, wherein only one outer surface of said tissue paper product has a polyhydroxy compound selected from the group consisting of glycerols, polyglycerols, polyethylene glycols (PEGS), polyoxyethylenes, polyoxypropylenes, and combinations thereof applied thereto by slot extrusion, said polyhydroxy compound providing said tissue paper product with a Wet Burst greater than about 90 g, a Dynamic Coefficient of Friction less than about 0.9, and a Bending Flexibility less than about 0.1 gf cm2/cm.

Abstract: The present invention provides a paper product having at least one ply, wherein only one outer surface of said tissue paper has a polyhydroxy compound and a lotion applied thereto.

Abstract: A tissue paper product having at least one ply, wherein only one outer surface of said tissue paper product has a polyhydroxy compound selected from the group consisting of glycerols, polyglycerols, polyethylene glycols (PEGS), polyoxyethylenes, polyoxypropylenes, and combinations thereof applied thereto by slot extrusion, said polyhydroxy compound providing said tissue paper product with a Wet Burst greater than about 90g, a Dynamic Coefficient of Friction less than about 0.9, and a Bending Flexibility less than about 0.1 gf cm2/cm.

Abstract: A tissue paper product having at least one ply, wherein only one outer surface of said tissue paper product has a polyhydroxy compound applied thereto by slot extrusion, said polyhydroxy compound providing said tissue paper product with a Wet Burst greater than about 90 g, a Dynamic Coefficient of Friction less than about 0.9, and a Bending Flexibility less than about 0.1 gf cm2/cm.

Abstract: An apparatus for testing the break-through strength of a tissue product is disclosed. The apparatus comprises a dose addition assembly having an opening and a sample holder. The sample holder comprises a lower platen and an upper platen disposed in a fact to face relationship and each having coextensive openings disposed therein. The opening of the dose addition assembly is disposed proximate to one of the openings disposed within the upper and lower platens. A substance is disposed within the dose addition assembly and is capable of being expectorated from the opening of the dose addition assembly through one of the openings disposed within the upper and lower platens onto a tissue product disposed between the upper and lower platens and within the openings disposed within the upper and lower platens.

Abstract: A method for testing the break-through strength of a tissue product is disclosed. The method entails the steps of: a) observing a first condition of the tissue product; b) disposing the tissue product between a lower platen and an upper platen; c) disposing at least a portion of the tissue product within an aperture disposed within the lower platen and an aperture disposed within the upper platen; d) providing a simulated mucous composition; e) directing the simulated mucous composition toward the tissue product disposed within the aperture disposed within the lower platen and the aperture disposed within the upper platen; f) after step d), observing a second condition of the tissue product; and, g) comparing the first and the second conditions of the tissue product.