JP2012024547A - Facial tissue product - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide a facial tissue product which has a facial tissue having smooth touch and moist feeling equal to or larger than those of conventional moist facial tissues, having reduced sticky feeling and hard to tear during use, and further hard to tear when taken out.SOLUTION: The facial tissue product has a two-ply facial tissue coated with a chemical liquid, and the tissue is constituted such that the chemical liquid is coated on both sides of the tissue at 1.5-5.0 g/m, sheets composing the two-ply tissue have a basis weight of 10-25 g/mper layer, and the thickness of the two-ply facial tissue sheets is 100-140 μm. A film constituting an outlet window 202a of a storage box 201 has a thickness of 33-38 μm, and a vertical bending resistance of 0.8-1.4 gf/10 mm.

Description

  The present invention relates to tissue paper and tissue paper products.

The tissue paper in the domestic market is broadly divided into non-moisturizing tissue and moisturizing tissue. Here, the moisturizing tissue is a tissue produced by applying a moisturizing agent such as glycerin to a tissue base paper that has been made, and the non-humidifying tissue is a general tissue that does not apply a moisturizing agent to the tissue base paper.
The use of tissue paper is mainly for personal use, mainly for facial use including nasal cover, and moisturizing tissue is considered to be a product specification specialized for nasal blow.
In the past, tissue paper has been used for facial applications, mainly for nasal clasps, and so many attempts have been made so far in order to pursue good touch and quality improvements have been repeated. For example, various softeners are added to the raw materials to improve the flexibility of the product. Many supple fibers with low fiber roughness are used. Fine creping by sticking when wet paper dryer is dried and adjusting per doctor. The softness and smoothness of the paper is achieved by technologies such as forming the surface, improving the surface properties by a calender, and adjusting the raw material beating rate to a low level while maintaining the lateral strength by adjusting the ratio of the web speed. Improvements have been made.

However, in order to further improve quality, non-moisturizing tissue has technical limitations and an increase in the number of people suffering from hay fever and allergic rhinitis has led to the development of moisturizing tissue that is now part of the tissue market. Accounted for.
Heavy users, such as allergic rhinitis and hay fever, bite their nose more than tens of times a day, and the nose and its surroundings are rubbed against tissue, causing mild inflammation and redness. Therefore, for such a user, a material having a small friction on the tissue surface, that is, a material having smoothness is preferably used. The moisturizing tissue applies an aqueous lotion solution containing a hygroscopic moisturizing agent such as glycerin to the base paper of the sanitary thin paper. Glycerin is less irritating to the skin as used in cosmetics, absorbs moisture and moistens and softens the tissue, forms a thin film on the surface of the tissue, and is clearly softer than ordinary non-applied tissue It is recognized as a differentiated product with a smooth touch. For example, a technique for externally applying an oily substance and a humectant has been introduced (Patent Document 1).

  In this way, moisturizing tissue is recognized and consumption is increasing, but some moisturizing tissue heavy users leave moisturizers on their skin after biting their nose and feel sticky, and some dislike this Exists. Regarding this sticky feeling, a method for improving the sticky feeling by changing the chemical composition such as blending organic and inorganic powders as in Patent Document 2 is also known.

  Conventionally, in the manufacture of moisturizing tissue, it is common to apply chemicals off-machine after the paper making process and the plying process, and then perform folding using a rotary interfolder, which is often used for manufacturing non-humidifying tissue. No multi-stand interfolder is manufactured.

  As a box tissue product, it is the mainstream to use a storage box (height of about 50 to 65 mm) that is reduced in height and reduced in size from the viewpoint of reducing the manufacturing cost and transportation cost of the box. When using a compact storage box, the tissue paper stored inside is usually compressed, and the outlet on the top of the storage box is used to eliminate the difficulty of removing the top layer of tissue paper due to compression. It is designed to be longer than the long side direction of the upper surface (Patent Document 3). However, in the moisturizing tissue, there is a problem that the tissue paper is difficult to be held in the take-out port due to its high slipperiness and falls into the storage box, making it difficult to pop up. On the other hand, in order to hold tissue paper in the take-out port, when taking measures such as reducing the take-out port and increasing the rigidity of the film arranged in the take-out port, there is a problem that it is easily broken when taking out the tissue paper. Can occur.

Japanese Patent Laid-Open No. 4-9121 JP 2007-143664 A Japanese Patent No. 40673320

  The first object of the present invention is to provide a tissue paper that has a smoothness and a moist feeling equivalent to or higher than those of conventional moisturizing tissue paper, and has reduced stickiness and tearability during use. The second problem of the present invention is that when storing the tissue paper, the storage box configured to be easy to take out, to maintain the ease of pop-up, and to be difficult to tear when taking out, is used. To provide tissue paper products.

The present invention that has solved the above problems is as follows.
<Invention of Claim 1>
A tissue paper product in which a two-ply tissue paper coated with a chemical on its surface is folded in a pop-up manner and stored in a substantially rectangular storage box,
The tissue paper has a drug content of 1.5 to 5.0 g / m ^{2 on} both sides,
The basis weight per layer of the sheet constituting 2 plies is 10 to 25 g / m ² ,
2-ply paper thickness is 100-140 μm,
The storage box is made of a paper box having an opening on the upper surface in parallel with the long side direction, the opening being covered with a film attached to the inner surface of the storage box, and the film is a slit parallel to the opening in the long side direction. Have
A tissue paper product in which the film has a thickness of 33 to 38 μm and a longitudinal bending resistance of 0.8 to 1.4 gf / 10 mm.

<Invention of Claim 2>
The tissue paper product of Claim 1 whose moisture content of the said chemical | medical solution is 1 to 15%.

<Invention of Claim 3>
The tissue paper product according to claim 1, wherein the dry tensile strength in the CD direction of the two plies of the tissue paper is 80 to 120 cN / 25 mm.

<Invention of Claim 4>
The tissue paper product according to claim 1, wherein a coefficient of static friction between sheets of the tissue paper is 0.50 to 0.65.

  By applying and infiltrating a chemical solution containing a predetermined amount of moisture into the sheet constituting the two-ply tissue paper, the crepe structure of the sheet is extended, and the tissue paper having a smooth surface is formed. Further, since the paper thickness is reduced and the fiber density is increased by the elongation, the strength between fibers is increased, and a tissue paper having a high tensile strength in the CD direction can be obtained. Whereas conventional moisturizing tissue applies a lotion solution to a thick base paper to create a film on the surface of the tissue to give the user smoothness, the present invention suppresses the thickness and the amount of solution applied, and provides a crepe structure. The surface is made smooth by stretching, thereby providing a smoothness higher than that of a conventional moisturizing tissue. In other words, the sticky feeling is reduced as a minimum amount of the lotion solution film on the tissue surface to make it feel smooth. Therefore, the drug content in the dry state is lower than that of conventional lotion type tissue paper, and it contains a sufficient amount of drug to exert its effect even though it does not easily cause stickiness when used. Therefore, it has enough moist and moisturizing properties. Furthermore, since the paper thickness is thin, it has a soft feeling in use as compared with the drug content.

  By using a multi-stand type interfolder, the manufacturing speed can be increased. When the multi-stand type interfolder is used, the manufactured tissue paper product has a form in which the consumer pulls out the tissue paper in the CD direction. However, the conventional moisturizing tissue does not have high paper strength, particularly the tensile strength in the CD direction, as compared to the non-humidifying tissue, so that a product manufactured by a multi-stand type interfolder is easily broken when pulled out. A problem is assumed.

  In the tissue paper product according to the present invention, as described above, the tissue paper has a strong tensile strength in the CD direction and a small coefficient of static friction, and is flexible as a tissue paper storage box on the film around the outlet. Is used, and the size of the outlet is specified. Thereby, even if the tissue paper is pulled in the CD direction and taken out, it is difficult to break, and the uppermost layer is difficult to fall into the box from the take-out port. When folding with a multi-stand type interfolder for moisture-retaining tissue paper, a continuous sheet containing moisture is processed while applying a relatively high tensile force in the MD direction and applying pressure in the thickness direction. The web bulk can be kept lower than when using a folder. By this effect, it can be stored in a compact storage box frequently used for non-humidifying tissue paper products.

  As described above, the present invention provides a tissue paper having a moist and smooth texture equal to or higher than that of a conventional moisturizing tissue, having less stickiness than the conventional moisturizing tissue, and having a high tensile strength in the CD direction. Is. In addition, since tissue paper can be pulled out from the storage box in the CD direction, a chemical-coated tissue paper product that can be manufactured at high speed using a multi-stand type interfolder is provided. Furthermore, the chemical | medical solution application | coating tissue paper products accommodated in the compact type | mold storage box are provided.

It is a figure which shows the apparatus outline | summary of the ply process of the tissue paper of 1st Embodiment which concerns on this invention. It is the schematic which shows an example of a multi stand type inter folder, and has shown the state seen from the front. It is the schematic which shows an example of a multi stand type inter folder, and has shown the state seen from the side. It is the schematic which shows an example of a multi stand type inter folder, and has shown the state seen from the front. It is a longitudinal cross-sectional view of the folded tissue paper. It is a principal part expansion perspective view of the site | part regarding a folding plate. It is a principal part expansion perspective view which shows how to fold a secondary continuous sheet (tissue paper). It is a principal part expansion perspective view which shows how to fold a secondary continuous sheet (tissue paper). It is a principal part expansion perspective view which shows how to fold a secondary continuous sheet (tissue paper). It is a figure which shows a mode that the (a) tissue paper bundle | flux of 1st Embodiment is accommodated in the storage box. (B) It is a partially broken figure which shows a mode that the tissue paper accommodated in the storage box is taken out. It is a figure which shows the measuring method of the MMD value of tissue paper. It is a perspective view which shows an example of the tissue paper product which concerns on this invention. It is an inner surface development view of the storage box of the tissue paper product of FIG. It is a perspective view which shows the other example of the tissue paper product which concerns on this invention. It is an inner surface expanded view of the storage box of the tissue paper product of FIG.

Hereinafter, embodiments of the present invention will be described in detail.
[Example of structure]
The base paper of the tissue paper according to the present invention has a ply structure in which two thin papers (hereinafter also referred to as sheets) are laminated.

[Thin paper]
On the other hand, as the raw pulp of the thin paper (sheet) constituting the tissue paper according to the present invention, for example, mechanical pulp such as ground wood pulp (GP), pressure-rise ground wood pulp (PGW), thermomechanical pulp (TMP), etc. : Chemical pulps such as semi-chemical pulp (SCP), softwood high yield unbleached kraft pulp (HNKP), softwood bleached kraft pulp (NBKP), hardwood unbleached kraft pulp (LUKP), hardwood bleached kraft pulp (LBKP), etc .: deink Examples include waste paper pulp such as depulp (DIP) and waste pulp (WP). The raw material pulp can be used by selecting one kind or two or more kinds. Preferably, a chemical pulp containing no filler or foreign matter is preferred. Further, the raw material pulp may contain woody materials such as straw pulp, bamboo pulp, kenaf pulp, and herbs.

  In particular, the raw material pulp is preferably a blend of NBKP and LBKP. Waste paper pulp may be blended as appropriate, but in terms of texture and the like, it is preferably composed only of NBKP and LBKP. In this case, the blending ratio is NBKP: LBKP = 20: 80 to 80:20. In particular, NBKP: LBKP = 30: 70 to 60:40 is desirable.

  On the other hand, in papermaking raw materials, other fiber raw materials include polyethylene terephthalate, polybutylene terephthalate, and polyester fibers such as copolymers thereof, polyolefin fibers such as polyethylene, polypropylene, and polystyrene, acrylics such as polyacrylonitrile and modacrylic. Fiber, polyamide fiber such as nylon 6, nylon 66, nylon 12, etc., synthetic fiber such as polyvinyl alcohol fiber, polyvinylidene chloride fiber, polyvinyl chloride fiber, urethane fiber, semi-synthetic fiber such as triacetate fiber, diacetate fiber, screw Include regenerated cellulose fiber such as coarse rayon, copper ammonia rayon, polynosic rayon, lyocell, and chemical fiber such as regenerated fiber spun from solution of collagen, alginic acid, chitin, etc. It is possible. The polymer constituting the chemical fiber may be in the form of a homopolymer, a modified polymer, a blend, a copolymer or the like.

  Raw materials such as pulp fibers are used as a base paper through, for example, a known papermaking process, specifically, a wire part, a press part, a dryer part, a calendar part, and the like. In this papermaking, for example, a dry paper strength enhancer, a wet paper strength enhancer, a softener, a release agent, a coating agent, a viscosity agent (knurl), a pH adjuster such as caustic soda, an antifoaming agent, a dye, etc. Chemicals can be added.

[US tsubo]
The rice paper weight per sheet of the tissue paper according to the present invention is preferably 10 to 25 g / m ² , more preferably 11 to 16 g / m ² . If the rice tsubo is less than 10 g / m ² , it is preferable from the viewpoint of improving softness, but it is difficult to ensure adequate strength that can withstand use. On the other hand, when the rice tsubo exceeds 25 g / m ² , the entire paper becomes hard, and a feeling of stickiness is generated, resulting in poor touch. In addition, the US tsubo is based on the US tsubo measurement method of JIS P 8124 (1998).

[Crepe rate]
The crepe rate of the primary raw sheet constituting the tissue paper of the present invention is 10 to 30%, more preferably 13 to 20%. Here, the crepe rate is expressed by the following equation.
Crepe rate: {(peripheral speed of the dryer during papermaking)-(peripheral speed of the reel)} / (peripheral speed of the dryer during papermaking) × 100.

[Medical solution]
Tissue paper of the present invention, the drug combined duplex 1.5~5.0g / m ^2, more preferably 3.0~5.0g / m ² containing. If the drug content is less than 1.5 g / m ² , the effect of the drug is not exhibited, and if it exceeds 5.0 g / m ² , the tissue paper has a sticky feeling, and the dry tensile strength decreases.

  About the chemical | medical solution to apply | coat, it is preferable that a viscosity shall be 1-700 mPa * s at 40 degreeC from a viewpoint of performing high-speed processing, especially 50-400 mPa * s. If it is less than 1 mPa · s, the chemical solution is likely to scatter on rolls such as anilox roll, printing plate roll, and gravure roll, and conversely if it is greater than 700 mPa · s, it is difficult to control the amount of application to each roll or continuous sheet. Ingredients include 70-90% polyol, 1-15% moisture, and 0.01-22% functional chemicals. The water content of the chemical solution to be applied was determined by the Karl Fischer method.

  Polyols include polyhydric alcohols such as glycerin, diglycerin, propylene glycol, 1,3-butylene glycol, polyethylene glycol, and derivatives thereof, and sugars such as sorbitol, glucose, xylitol, maltose, maltitol, mannitol, and trehalose.

  Functional agents include softeners, surfactants, inorganic and organic fine particle powders, oily components, and the like. Softeners and surfactants have the effect of imparting flexibility to the tissue and smoothing the surface, and anionic surfactants, cationic surfactants and zwitterionic surfactants are applied. Inorganic and organic fine particle powders have a smooth surface. The oil component has a function of improving lubricity, and higher alcohols such as liquid paraffin, cetanol, stearyl alcohol, and oleyl alcohol can be used.

  In addition, as a functional agent, one of a hydrophilic polymer gelling agent, collagen, hydrolyzed collagen, hydrolyzed keratin, hydrolyzed silk, hyaluronic acid or a salt thereof, ceramide, etc. A moisturizing agent such as any combination can be added.

  Deodorants such as flavors, emollients such as various natural extracts, vitamins, emulsifiers that stabilize compounding ingredients, antifoaming agents, antifungal agents, organic acids, etc. An agent can be appropriately blended. Furthermore, you may contain the antioxidant of vitamin C and vitamin E.

Of the above components, it is preferable to use a polyhydric alcohol such as glycerin or propylene glycol as a main component in order to stabilize the viscosity and coating amount of the chemical solution.
The temperature at the time of chemical solution application is preferably 30 ° C to 60 ° C, preferably 35 ° C to 55 ° C.

[Amount of application]
The coating amount was calculated from the difference between each sheet basis weight when the chemical solution after ply was not applied during operation and each sheet basis weight immediately after the corresponding application.
(Coating amount g / m ²⁾ = (basis weight g / m ² immediately after coating) - (the basis weight g / m ² in the case of not applying)
The coating amount of both surface layers or the total coating amount of both surfaces is the total coating amount per unit area of the plyed tissue paper sheet, and the coating amount of each sheet is added.

[Drug content]
The drug application amount indicates the content of the drug component in a dry state (absolutely dry) included in the unit area of tissue paper in the standard state of JIS P 8111 (1998). Specifically, in the applied chemical solution The content of components other than moisture shall be indicated. The unit area of the tissue paper is an area of the plyed sheet viewed from a viewpoint perpendicular to the plane, and does not mean the total area of each plyed sheet and its front and back surfaces.

[Drug content]
The chemical content is defined as a tissue paper product having a predetermined mass conditioned under JIS P 8111 (1998) as a denominator (A) (g), and the water content in the chemical solution contained in the tissue paper product having a predetermined mass. The ratio of (B) divided by (A) is expressed as (%), with the removed mass (B) (g) as a molecule.
(Drug content%) = (B) ÷ (A) × 100 (%)

[Drug density]
The chemical solution density is the drug content per volume of two-ply tissue paper in the standard state of JIS P 8111 (1998).

[Paper thickness]
The paper thickness of the tissue paper according to the present invention is 100 to 140 μm, more preferably 120 to 140 μm in a 2-ply state. If the paper thickness is less than 100 μm, it is preferable from the viewpoint of improving the softness, but it is difficult to ensure adequate strength as tissue paper. On the other hand, when the thickness exceeds 140 μm, the texture of the tissue paper is deteriorated and a feeling of tingling is generated during use.

  As a method for measuring the paper thickness, the specimen is fully conditioned under the conditions of JIS P 8111 (1998), and then the dial thickness gauge (thickness measuring instrument) “PEACOCK G type” (manufactured by Ozaki Seisakusho) under the same conditions. It shall be measured in the state of 2 plies using. Specifically, confirm that there is no dust, dust, etc. between the plunger and the measuring table, lower the plunger on the measuring table, move the memory of the dial thickness gauge to adjust the zero point, and then Raise the plunger, place the sample on the test bench, slowly lower the plunger and read the gauge at that time. At this time, only the plunger is placed. The terminal of the plunger is made of metal so that a circular plane having a diameter of 10 mm is perpendicular to the plane of the paper, and the load at the time of measuring the paper thickness is about 70 gf. The paper thickness is an average value obtained by performing measurement 10 times.

[Tensile strength]
The tensile strength of the tissue paper according to the present invention is measured in a two-ply state.
The dry tensile strength is measured according to the tensile test method of JIS P 8113 (1998). Among them, it is cut into a width of 25 mm in the vertical direction and the horizontal direction under the standard conditions defined in JIS P 8111 (1998).

  The dry tensile strength of the tissue paper according to the present invention is 180 to 350 cN / 25 mm in the MD direction, more preferably 160 to 300 cN / 25 mm, 80 to 120 cN / 25 mm in the CD direction, and more preferably 80 to 110 cN / 25 mm. The ratio of the direction / CD direction is preferably 1.5 to 3.0.

  The wet tensile strength is determined according to JIS P 8135 (1998). The wet tensile strength of the tissue paper is 70 to 160 cN / 25 mm in the MD direction, more preferably 80 to 130 cN / 25 mm, and 33 to 50 cN / 25 mm, more preferably 35 to 45 cN / 25 mm in the CD direction.

[Softness]
The softness value of the tissue paper of the present invention is preferably 0.80 to 1.10 cN / 100 mm. The softness here is measured based on the handle ohm method according to the JIS L 1096 E method.
However, the test piece was 100 mm × 100 mm in size, and the clearance was 5 mm. The measurement was performed 5 times each in the longitudinal direction and the lateral direction with 1 ply, and the average value of all 10 times was represented by 2 digits of decimal point and expressed in units of cN / 100 mm.

  By setting the softness within the above range, it is possible to reduce the resistance value when taking out the tissue paper to make it difficult to break, and to balance the feeling of thickness and softness.

〔Moisture percentage〕
The moisture content of the product is desirably 10.0 to 13.0%. The moisture content is determined based on JIS P 8127.
Moisture content (%) = {(weight of paper before drying) − (weight of paper after drying)} / (weight of paper before drying) × 100

〔Growth rate〕
The elongation in the MD direction of the product is desirably 11.0 to 15.0%. The elongation rate here is measured using “Universal Tensile Compression Tester TG-200N” manufactured by Minebea Co., Ltd. The elongation is the “stretch at break” described in “3. Definition e)” of JIS P8113.

[Static friction coefficient]
On the other hand, the tissue paper of the present invention desirably has a coefficient of static friction between tissue papers of 0.50 to 0.65, more preferably 0.55 to 0.60. The static friction coefficient here is measured by the following method according to JIS P 8147 (1998).
The tissue paper peeled off in one ply is attached to the acrylic plate so that the outer surface of the tissue paper is on the outside. Wrap tissue paper around a 100 g weight with 2 plies and place it on the tissue on the acrylic plate. Tilt the acrylic plate and measure the angle at which the weight slides down. Angle measurement is carried out 10 times in total, 5 times for each of the tissue in the vertical and vertical directions (MD and MD directions), and in the horizontal and horizontal directions (CD and CD directions), and the average angle is calculated. The tangent value is defined as a coefficient of static friction.

  The following can be considered as a principle for reducing the static friction coefficient. In the present invention, two primary raw fabric continuous sheets are plyed, the crepe peak is smoothed by calendering, the sheet surface is smoothed by smoothing the crepe peak, and then the lotion chemical solution Is preferably applied by a transfer method. The applied secondary raw sheet is stored under a certain tension and seasoned until it is folded. During this time, the lotion chemical solution spreads over time so as to be uniform inside the paper layer in a planar and thickness direction. In the subsequent process, when folding by the multi-stand type interfolder is performed, the secondary continuous sheet is pulled out from the ply raw fabric, folded, and cut through a process of pressing with a pull conveyor while pulling. In this folding process, folding processing is started in a state in which it is coated and seasoned and moisture is absorbed in the paper layer. Due to seasoning and subsequent tension and pressure in the thickness direction, unevenness due to creping on the sheet surface is reduced, and friction between sheets is reduced.

[MMD]
MMD is an average deviation (unit: dimensionless) of the friction coefficient μ. MMD is one of the indices of smoothness. The smaller the numerical value, the smoother, and the larger the numerical value, the less smooth.
As a method for measuring the MMD value, as shown in FIG. 11A, a tension of 20 g / cm is applied to the contact surface of the friction element 112 in a predetermined direction (downward and rightward in FIG. 11A). While being brought into contact with the surface of the tissue paper 111, which is the measurement sample, at a contact pressure of 25 g, it is moved 2 cm at a speed of 0.1 cm / s in the same direction as the direction in which the tension is applied. At this time, the friction coefficient was measured using a friction tester KES-SE (manufactured by Kato Tech Co., Ltd.), and the average deviation of the friction coefficient μ at a friction distance of 2 cm (moving distance was 3 cm and excluding 5 mm before and after each). Was defined as the MMD value.
The friction element 112 has 20 piano wires P with a diameter of 0.5 mm adjacent to each other, and has a contact surface formed so that the length and width are both 10 mm. The contact surface is formed with a unit bulging portion whose tip is formed of 20 piano wires P (curvature radius 0.25 mm).
FIG. 11A schematically shows the friction element 112, and FIG. 11B shows an enlarged view of a portion surrounded by an alternate long and short dash line in FIG. 11A.

[Web bulk]
A plastic plate having a weight of 30 g and a size of 130 mm × 250 mm was placed on the tissue paper bundle, and the heights of the four corners were averaged to obtain the web bulk value.
The web volume of the tissue paper according to the present invention is 0.25 to 0.40 mm per set. In particular, it is preferably 0.28 to 0.36 mm per set and 55 to 65 mm for 180 sets. If the web bulk is too low, it becomes difficult for the user to put the finger deeply out of the take-out opening when taking out the uppermost tissue from the storage box, making it difficult to take out. Further, if the web bulk is too high, it cannot be stored in a compact storage box (having a box height of about 55 to 65 mm), and manufacturing costs and transportation costs are increased, or the web is compressed during storage and is compact. In order to store in the storage box, the top layer must be pulled out with a strong force when taking out, and there is a problem that the tissue paper is easily torn.

[Product density]
The tissue paper according to the present invention is folded by an interfolder or the like, and is cut into a product size at any stage before or after the folding process. For example, 180 sets are packed into a product. The paper density after 180 sets of folding is preferably 0.15 to 0.25 g / cm ³ , more preferably 0.17 to 0.23 g / m ³ . If it is lower than 0.15 g / cm ³ , moist feeling and smoothness cannot be obtained, and if it is higher than 0.25 g / cm ³ , the thickness of the tissue paper is impaired and a sticky feeling is produced, and the water absorption is deteriorated. End up.
The product density is the paper thickness (D) of tissue paper (2 ply) according to “PEACOCK G type”, which is a double value (C) of the tissue paper product tsubo conditioned under JIS P 8111 conditions. The unit is expressed in g / cm ³ and 3 decimal places.
((Density (g / cm ³ )) = (C (g / m ² )) × 2 ÷ (D (μm))

[Storage box]
12 shows a tissue paper product according to the present invention, and FIG. 13 shows a view of the storage box 201 as seen from the inside of the box in the unfolded state. As a material for forming the box, any known material used as a tissue paper storage box such as cardboard having a basis weight of 300 to 450 g / m ² can be used. The tissue paper storage box 201 has a rectangular parallelepiped shape in an assembled state as shown in FIG. 12, and includes a pair of upper and lower upper surfaces 202 and 203, a pair of front and rear front surfaces 204 and 205, and a pair of left and right left sides. A surface 204 and a right side 205. In this case, the front and rear surfaces 204 and 205 and the left and right side surfaces 206 and 207 correspond to the peripheral surface of the present invention.

  As can be seen from the developed state of FIG. 13, the adhesive margin piece 203b extends from the rear edge of the lower surface (the edge adjacent to the rear surface of the peripheral edge) over the entire long side, and the adhesive margin piece 203b overlaps the inner side of the rear surface. Then, a cylindrical portion composed of the upper surface 202, the lower surface 203, the front surface 204, and the rear surface 205 is formed by being bonded and fixed by an adhesive such as a hot melt adhesive.

  The left and right side surfaces 204 and 205 extend from an adjacent edge of the upper surface 202 and an adjacent edge of the lower surface 203, respectively, and from an adjacent edge of the front surface 204 and an adjacent edge of the rear surface 205, respectively. The front flap 204f and the rear flap 205f, the upper flap 202f and the lower flap 203f are overlapped on the outside of the front flap 204f and the rear flap 205f, and the upper flap 202f and the lower flap 203f are the front flap and the rear flap 205f. The lower end portion of the upper flap 202f is overlapped on the outer side of the upper end portion of the lower flap 203f, and the overlapped portion is fixed by the adhesive.

  The inner dimension of the box is preferably 5 to 20 mm, particularly 8 to 15 mm longer than the length in the longitudinal direction of the web to be stored. By providing a gap in the longitudinal direction inside the storage box, it becomes possible to take out the tissue paper with almost no resistance between the inner surface of the box and the tissue paper.

  The height of the storage box can be arbitrarily determined within the scope of the present invention in accordance with the number of web sets to be stored, but considering the economic efficiency and convenience of use, the number of web sets is set to 150 to 300 sets. The height of the storage box is preferably 50 to 120 mm.

  Furthermore, the height of the storage box is preferably 50 to 80 mm, more preferably 55 to 65 mm, in order to reduce manufacturing costs and transportation costs.

  A cutout such as a perforation is formed in advance on the upper surface 202 of the storage box 201, and an extraction window (opening) 202a is formed by peeling off the lid portion 202b surrounded by the cutout at the start of use. It has become. As shown in FIGS. 14 and 15, the lid portion 202 b may be configured so as to be a valley fold line 202 g without being cut off at substantially one side. By setting it as such a structure, the cover part 2b can be utilized as a cover of the extraction window 202a. Alternatively, the take-out window 202a may be opened in advance and the lid portion 202b may not be provided. The length in the long side direction of the take-out window 202a is 50 to 70%, particularly 55 to 65% of the length in the longitudinal direction of the web to be stored. The length in the short side direction of the take-out window 202a is preferably 35 to 55%, particularly 40 to 50% of the length in the short side direction of the web.

  A film-like cover sheet 202c is attached to the take-out window 202a from the inside of the box with a hot-melt adhesive or the like, and a portion of the cover sheet 202c surrounded by the take-out window 202a has a long side direction of the box 1 A slit 202s is formed. The slit 202s is 45 to 65%, particularly 50 to 60% of the length in the longitudinal direction of the web to be stored. The slit 202s is particularly preferably arranged in the vicinity of the center of the extraction window 202a in both the long side direction and the short side direction.

  As a material for forming the cover sheet, a resin film sheet made of a resin such as polyethylene, polypropylene, polyester, or a laminated resin film sheet obtained by laminating these, a laminated film sheet laminated with a film sheet and a thin paper, etc. Examples include synthetic paper sheets made of fibers. A resin film sheet is preferable in consideration of the take-out property, and a low-density polyethylene film (LDPE) that is particularly flexible and low in production cost can be suitably used.

  The thickness of the film is desirably 33 to 38 μm. Further, it is preferable that the longitudinal bending resistance of the film is 0.8 to 1.4 gf / 10 mm, particularly 1.0 to 1.2 gf / 10 mm. The bending resistance was measured based on the handle ohmmeter method described in JIS L 1096 E method. The test piece was 100 mm long × 10 mm wide, and the clearance was 5 mm. The average value of 10 times in 1 ply in the vertical direction was represented by 2 digits of decimal point and expressed in units of cN / 100 mm. The longitudinal direction of the film coincides with the slit direction of the film. If the bending resistance of the film in the longitudinal direction is higher than 1.4 gf / 10 mm, it will be easy to tear when taking out the tissue paper, and if it is lower than 0.8 gf / 10 mm, it will be difficult to hold the tissue paper in the outlet and pop-up will occur. It becomes difficult.

  Furthermore, the coefficient of static friction between the lateral direction of the film and the tissue paper (the removal direction) is 0.20 to 0.30, more preferably 0.23 to 0, in order to improve the slip of the tissue paper at the time of taking out and suppress the resistance. .28. The film transverse direction means a direction perpendicular to the film longitudinal direction and the film plane. The coefficient of static friction between the film and tissue paper was measured by the following method. The film is affixed to the acrylic plate so that the slope direction is the lateral direction of the film so that the inner surface of the storage box is on the outside. Wrap tissue paper around a 100 g weight with 2 plies, and place it on the film on the acrylic plate so that the slope direction is the tissue removal direction. Tilt the acrylic plate and measure the angle at which the weight slides down. The angle measurement was performed 10 times, the average angle was calculated, and the tangent value was taken as the static friction coefficient.

[Tissue paper removal resistance]
By setting the resistance applied when taking out the tissue paper within a certain range, it is possible to minimize tearing during the taking out. The tissue paper take-out resistance is measured by the following method. Secure the center tip of tissue paper to the gauge tip of the pushbull gauge, and take the tissue paper vertically from the storage box with the bottom surface fixed at a constant speed over a period of 0.4 to 0.6 seconds. The resistance value was measured. The tissue paper to be taken out is a total of 5 sets from the first set to the 5th set from the top layer, and a total of 5 sets from the 11th set to the 15th set. It was. The take-out resistance is preferably 70 gf or less, more preferably 50 to 70 gf.

[Example of manufacturing method]
The tissue paper of the present invention described above can be manufactured as follows. In FIG. 1, the outline | summary of the apparatus of the ply process of the tissue paper which concerns on this invention was shown. In addition, it is preferable to implement the process which concerns on FIG. 1 with the ply machine which is an apparatus integrated with the coating device (on-machine coating).

  The base paper produced by the paper machine is creped as a continuous sheet, calendered, and wound up to form primary rolls 11 and 12 (generally also called jumbo rolls). The

  The continuous sheets 31 and 32 are laminated by the laminating roller 13 to form two plies, and if necessary, calendered by the ply machine calendar 14 and sent to the chemical solution coating process. Any known coating method such as dipping, spraying, flexo coating, and gravure coating can be used as the chemical coating method, but printing methods such as gravure coating and flexographic coating that perform chemical coating evenly on the entire coated surface In particular, it is more preferable to use a flexo coater equipped with a doctor chamber 15 because a chemical solution can be supplied in a stable coating amount.

  In the ply process of FIG. 1, two flexo coaters 16 and 17 are provided, and a chemical solution is applied to each surface of a two-ply continuous sheet.

  When the flexographic printing method is used as the chemical solution applying means, the processing speed is 100 to 1100 m / min, preferably 350 to 1050 m / min, particularly preferably 450 to 1000 m / min. If it is less than 100 m / min, the productivity is low, and if it is more than 1100 m / min, uneven coating occurs and the chemical solution is likely to scatter. The number of lines of the flexographic printing plate roll is 10 to 60 lines, preferably 15 to 40 lines, and particularly preferably 20 to 35 lines. If the number of lines is less than 10, many coating irregularities occur. On the other hand, if the number of lines exceeds 60 lines, the paper dust tends to clog. The number of lines of anilox roll is 10 to 300 lines, preferably 25 to 200 lines, particularly preferably 50 to 100 lines. If the number of lines is less than 10, many coating irregularities occur. On the other hand, if the number of lines exceeds 300 lines, the paper dust tends to be clogged. The anilox roll has a cell capacity of 10 to 100 cc, preferably 15 to 70 cc, particularly preferably 30 to 60 cc. If the cell capacity is less than 10 cc, a desired coating amount cannot be obtained. On the other hand, if the cell capacity is more than 100 cc, the amount of chemical solution scattered increases. By setting it as such a structure, a chemical | medical solution is transcribe | transferred to the crepe peak part of a continuous sheet in the shape of a dot of 1 mm or less, and a uniform application | coating sheet is obtained.

The flexographic printing method can stabilize the coating amount even when the processing speed is high, and can stably apply a wide range of chemical viscosity with a single roll.
When the gravure printing method is used as the chemical solution applying means, the processing speed is 100 to 1000 m / min, preferably 350 to 950 m / min, particularly preferably 450 to 950 m / min. When it is less than 100 m / min, productivity is low, and when it is more than 1000 m / min, coating unevenness occurs and the chemical solution is likely to be scattered. The number of gravure rolls is 40 to 160 lines, preferably 60 to 140 lines, particularly preferably 80 to 120 lines. If the number of lines is less than 40 lines, the amount of chemical solution scattered increases, whereas if the number of lines exceeds 160 lines, paper dust tends to be clogged.

  When the chemical spraying method is used as the chemical coating means, the spraying means is not particularly limited, but may be a nozzle dampening method or a rotor dampening spraying method. The processing speed is 100 to 1100 m / min, preferably 350 to 1050 m / min, and more preferably 450 to 1000 m / min.

  The sheet after application of the chemical solution is supplied to a contact embossing roller 18 and a roller roll 19 and fixed by subjecting a two-ply continuous sheet to a contact embossing (knurling) process. At this time, the continuous sheet 32 with a small amount of chemical solution applied is disposed so as to contact the contact embossing roller 18. The contact embossing is preferably applied uniformly in the vertical direction with a width of 1 to 10 mm at positions of 1/10 to 1/20 with respect to the paper width from both sides. Any of the known methods such as fixing the ply with an adhesive may be used. However, when using an adhesive, there is a problem that the touch tends to become hard, and it is easy to peel off when applying a chemical solution. It can be said that the use of embossing is more preferable.

2 ply continuous sheet with contact embossing is cut directly into product size after being subjected to folding processing by being directly applied to a rotary interfolder or the like, or after being cut into product width by slitter 20, The winding roll 21 makes a take-up secondary raw roll 22 which is folded and stored in a paper box.
In this embodiment, the chemical solution is applied before the contact embossing. However, the chemical solution may be applied after the contact embossing.

  Chemical solution application may be performed either on-machine or off-machine. Further, the chemical solution applying means may be provided before the winding process of the primary continuous sheet of the paper machine (if the calendar process is performed, it may be before or after the calendar process) or before the interfolder is folded. Furthermore, the chemical solution application means is not limited to a single one, and may be configured to apply the chemical solution in a plurality of steps.

[Multi-stand type inter folder]
The secondary raw roll described above is subjected to a folding process particularly in tissue paper products. As the folding process, a known method such as a rotary interfolder or a multi-stand interfolder can be used, but it is more preferable to use a multi-stand interfolder with high productivity. In the present invention, as described above, it is necessary to use a multi-stand type interfolder because the static friction coefficient of tissue paper needs to be low and the web bulk needs to be low.

  A large number of secondary web rolls 22 are set in a multi-stand type interfolder, and a tissue paper bundle is manufactured by drawing out a secondary continuous sheet from the set secondary web roll 22 and folding and stacking them. Hereinafter, an example of the multi-stand type interfolder will be described.

  2 and 3 show an example of a multi-stand type interfolder. Reference numeral 2 in the drawing denotes secondary raw rolls 22, 22... Set on secondary raw roll support portions (not shown) of the multi-stand type interfolder 1. These secondary raw rolls 22, 22... Are set side by side in the direction (the horizontal direction in FIG. 2, the front-to-back direction in FIG. 3) in which the required number is orthogonal to the illustrated plane. Each secondary raw roll R has slits in the width of tissue paper product in the above-described manufacturing equipment and manufacturing method of the secondary raw roll for tissue paper products. It is wound and set in double width.

  The continuous belt-like secondary continuous sheets 63A and 63B unwound from the secondary raw roll 22 are guided by guide means such as guide rollers G1 and G1 and fed into the folding mechanism section 60. Moreover, the folding mechanism part 60 is provided with the folding plate group 64 in which the required number of folding plates P, P ... are arranged in parallel as shown in FIG. For each folded plate P, guide rollers G2, G2 and guide round bar members G3, G3 for guiding a pair of continuous secondary continuous sheets 63A or 63B are respectively provided at appropriate positions. Further, below the folded plates P, P..., A conveyor 65 is provided that receives and conveys the laminated band 67 that is stacked while being folded.

  A folding mechanism using this type of folded plates P, P... Is a known mechanism, for example, from US Pat. As shown in FIG. 5, this type of folding mechanism folds each continuous secondary continuous sheet 63A, 63B... In the Z-shape and is adjacent to the adjacent secondary continuous sheets 63A, 63B. Stack the ends together.

  FIGS. 6 to 9 show in detail the portions of the folding mechanism 60 that are particularly related to the folded plate P. FIG. In the folding mechanism 60, a pair of continuous secondary continuous sheets 63A and 63B are guided for each folded plate P. At this time, the continuous secondary continuous sheets 63A and 63B are guided by the guide round bar members G3 and G3 while being shifted in position so that the side end portions do not overlap each other.

  The continuous secondary continuous sheet that overlaps the lower side when guided by the folded plate P is the first continuous secondary continuous sheet 63A, and the continuous secondary continuous sheet that overlaps the upper side is the second continuous sheet. As shown in FIGS. 5 and 7, these continuous secondary sheets 63A and 63B are second continuous secondary continuous sheets of the first continuous secondary continuous sheet 63A. The side end e1 that does not overlap the sheet 63B is folded back to the upper side of the second continuous secondary continuous sheet 63B by the side plate P1 of the folded plate P, and as shown in FIG. 5 and FIG. The side end portion e2 of the continuous secondary continuous sheet 63B that does not overlap the first continuous secondary continuous sheet 63A is folded downward so as to be drawn under the folded plate P from the slit P2 of the folded plate P. . At this time, as shown in FIGS. 5 and 9, the side end e3 (e1) of the continuous secondary continuous sheet 63A stacked while being folded in the upstream folded plate P is second from the slit P2 of the folded plate P. Are guided between the folded portions of the secondary continuous sheet 63B. In this way, each continuous secondary continuous sheet 63A, 63B... Is folded in a Z shape and the side ends of adjacent continuous secondary continuous sheets 63A and 63B are crossed together, so that the product is used. In some cases, when the top tissue paper is pulled out, the side edge of the next tissue paper is pulled out.

  As shown in FIG. 2, the laminated band 70 obtained in the multi-stand type interfolder 6 as described above is cut (cut) at a predetermined interval in the flow direction FL by the cutting means 66 at the subsequent stage, and the tissue is cut. This tissue paper bundle 30a is further stored in the storage box B in the subsequent equipment as shown in FIG. 10 (a). In the multi-stand type interfolder 1 as described above, the paper direction of the laminated band 70 is the vertical direction (MD direction) along the flow direction FL, and the horizontal direction along the direction orthogonal to the flow direction. Direction (CD direction). For this reason, the direction of the paper of the tissue paper constituting the tissue paper bundle 67a obtained by cutting the laminated band 70 into a predetermined length is along the folding direction of the tissue paper as shown in FIG. The horizontal direction (CD direction) and the vertical direction (MD direction) along the direction orthogonal to the folding direction of the tissue paper.

  FIG. 10B shows an example of a product in which the tissue paper bundle 67a is stored in the storage box B. A perforation M is provided on the upper surface of the storage box B, and a part of the upper surface of the storage box B is broken by the perforation M so that the upper surface of the storage box B is opened. The opening is covered with a film F having a slit at the center, and the tissue paper T can be taken out through the slit provided in the film F.

  By the way, as described above, the direction of the paper of the tissue paper constituting the tissue paper bundle 67a is the horizontal direction (CD direction) along the folding direction of the tissue paper, as shown in FIG. When the tissue paper T is pulled out from the storage box B, the pulling direction is along the horizontal direction (CD direction) of the tissue paper T.

In order to confirm the effect of the present invention, Table 1 shows the results of evaluating the dimensions of the product and the paper quality of the tissue paper for the examples and comparative examples according to the present invention.
Examples 1 to 7 are tissue papers according to the present invention manufactured using a multi-stand type interfolder for folding.

  Comparative Examples 1 to 4 are commercially available products, Comparative Example 1 is a non-moisturizing general purpose tissue paper, and Comparative Examples 2 to 4 are moisturizing lotion type tissue papers.

  The composition of the chemical solution applied to Examples 1 to 7 was adjusted as shown in Table 2. The method for measuring tissue weight, paper thickness, tensile strength, elongation, softness, coefficient of static friction, moisture content, MMD, and tissue resistance of tissue paper is described in the section of the embodiment for carrying out the invention. Just as you did. The drug content indicates the ratio of the dry weight of the drug to the tissue paper basis weight.

  Table 1 shows the inner dimensions of the storage boxes for the tissue paper products of Examples 1 to 7 and Comparative Examples 1 to 4, the dimensions of the take-out window, the length of the slit, the material, thickness, and Clark stiffness of the film.

Along with the evaluation of paper quality, sensory evaluation based on the following criteria was performed for 10 people in Examples 1 to 7 and Comparative Examples 1 to 4 for softness, smoothness, thickness, and moist feeling. The sensory evaluation was performed on the basis of the following criteria, with all results of Comparative Example 1 being a non-humidifying tissue paper set to 3.
5: Very good 4: Excellent 3: Equivalent to the standard 2: Inferior 1: Notably inferior The tissue-coated tissue paper was also evaluated for the presence or absence of stickiness.
○: Little sticky feeling ×: Clearly sticky feeling
The ease of taking out the tissue paper was evaluated as follows by carrying out the taking out operation for 10 people.
○: Resistance at the time of taking out was small, and there was no tear.
Δ: 1 to 4 people broke or complained of difficulty in taking out due to resistance.
X: Five to ten people complained of tearing.
Regarding the presence or absence of the tissue paper in the storage box, for 10 people, all tissue paper products were taken out from the first set to determine whether or not there was any depression.
○: There was no depression.
Δ: 1 to 4 people experienced a drop once or more.
X: 5-10 people experienced the depression once or more.
The difficulty of tearing at the time of use was evaluated by using tissue paper as a nose for 10 persons and determining whether there was any tear.
○: 3 or fewer people were torn or not torn.
Δ: 4 to 8 people were torn.
X: 9 to 10 persons were torn.

The tissue paper according to the present invention showed high values of the dry tensile strength and the wet tensile strength in the CD direction as compared with a commercially available moisturizing tissue. The wet tensile strength in the CD direction was higher than that of conventional general-purpose tissue paper. It was also shown that the softness and static friction coefficient were lower than those of commercial products, and the paper was smooth and soft.
In sensory evaluation, the tissue paper according to the present invention is not excellent in thickness, but has a softness, smoothness, moist feeling equal to or higher than that of a moisturizing tissue, and a sticky feeling seen in a moisturizing tissue. I found out that it was alleviated.

  In particular, the following factors can be considered as factors that have good slipperiness for the tissue paper according to the present invention. Although it depends on the permeability of the chemical applied to tissue paper, when a chemical containing both hydrophilic and lipophilic components is applied, the hydrophilic components are absorbed into the pulp and the lipophilic components tend to remain on the paper surface. It is considered that surface friction is reduced. However, increasing the amount of chemical solution applied as in conventional moisturizing tissue, the hydrophilic component is not sufficiently absorbed into the pulp and remains on the surface, reducing the friction-reducing effect of the lipophilic component and hydrophilic components (such as glycerin). It is presumed that the slipperiness decreases due to the viscosity of.

In Examples 1 to 7, significantly better results than Comparative Examples 1 to 3 were obtained regarding the resistance to taking out tissue paper and the ease of taking out tissue paper. Thereby, it can be said that the risk of tearing at the time of taking out was reduced because slipping when taking out the tissue paper was good and the tissue paper could be taken out smoothly. In Comparative Example 4, there is a gap between the web and the inner surface of the upper portion of the box, and the web is softly inserted. Therefore, friction between the sheets hardly occurs, and the take-out resistance is small. However, the comparative example 4 has a problem that the sheet is likely to drop during use and is difficult to pop up. Compared with this, even if Example 1-4 improves sliding, it turns out that the tissue paper in use does not fall into the inside of a storage box from a slit part, and does not impair a usability even in the middle of use. It was.
Moreover, in Comparative Examples 2-4, it turned out that the tear at the time of use tends to arise, but Examples 1-7 are hard to produce a tear.

  As described above, the tissue paper according to the present invention has a sticky feeling seen in conventional moisturizing tissue and has a softness, smoothness, and moist feeling equivalent to or higher than that of the moisturizing tissue. It turned out to be. Further, it was found that the tissue paper can be taken out smoothly and is not easily torn at the time of taking out.

  The tissue paper and tissue paper product of the present invention can be used for tissue paper and tissue paper products used for wiping applications, in particular, body wiping applications, and facial applications.

  The present invention relates to tissue paper and tissue paper products.

The tissue paper in the domestic market is broadly divided into non-moisturizing tissue and moisturizing tissue. Here, the moisturizing tissue is a tissue produced by applying a moisturizing agent such as glycerin to a tissue base paper that has been made, and the non-humidifying tissue is a general tissue that does not apply a moisturizing agent to the tissue base paper.
The use of tissue paper is mainly for personal use, mainly for facial use including nasal cover, and moisturizing tissue is considered to be a product specification specialized for nasal blow.
In the past, tissue paper has been used for facial applications, mainly for nasal clasps, and so many attempts have been made so far in order to pursue good touch and quality improvements have been repeated. For example, various softeners are added to the raw materials to improve the flexibility of the product. Many supple fibers with low fiber roughness are used. Fine creping by sticking when wet paper dryer is dried and adjusting per doctor. The softness and smoothness of the paper is achieved by technologies such as forming the surface, improving the surface properties by a calender, and adjusting the raw material beating rate to a low level while maintaining the lateral strength by adjusting the ratio of the web speed. Improvements have been made.

However, in order to further improve quality, non-moisturizing tissue has technical limitations and an increase in the number of people suffering from hay fever and allergic rhinitis has led to the development of moisturizing tissue that is now part of the tissue market. Accounted for.
Heavy users, such as allergic rhinitis and hay fever, bite their nose more than tens of times a day, and the nose and its surroundings are rubbed against tissue, causing mild inflammation and redness. Therefore, for such a user, a material having a small friction on the tissue surface, that is, a material having smoothness is preferably used. The moisturizing tissue applies an aqueous lotion solution containing a hygroscopic moisturizing agent such as glycerin to the base paper of the sanitary thin paper. Glycerin is less irritating to the skin as used in cosmetics, absorbs moisture and moistens and softens the tissue, forms a thin film on the surface of the tissue, and is clearly softer than ordinary non-applied tissue It is recognized as a differentiated product with a smooth touch. For example, a technique for externally applying an oily substance and a humectant has been introduced (Patent Document 1).

  In this way, moisturizing tissue is recognized and consumption is increasing, but some moisturizing tissue heavy users leave moisturizers on their skin after biting their nose and feel sticky, and some dislike this Exists. Regarding this sticky feeling, a method for improving the sticky feeling by changing the chemical composition such as blending organic and inorganic powders as in Patent Document 2 is also known.

  Conventionally, in the manufacture of moisturizing tissue, it is common to apply chemicals off-machine after the paper making process and the plying process, and then perform folding using a rotary interfolder, which is often used for manufacturing non-humidifying tissue. No multi-stand interfolder is manufactured.

  As a box tissue product, it is the mainstream to use a storage box (height of about 50 to 65 mm) that is reduced in height and reduced in size from the viewpoint of reducing the manufacturing cost and transportation cost of the box. When using a compact storage box, the tissue paper stored inside is usually compressed, and the outlet on the top of the storage box is used to eliminate the difficulty of removing the top layer of tissue paper due to compression. It is designed to be longer than the long side direction of the upper surface (Patent Document 3). However, in the moisturizing tissue, there is a problem that the tissue paper is difficult to be held in the take-out port due to its high slipperiness and falls into the storage box, making it difficult to pop up. On the other hand, in order to hold tissue paper in the take-out port, when taking measures such as reducing the take-out port and increasing the rigidity of the film arranged in the take-out port, there is a problem that it is easily broken when taking out the tissue paper. Can occur.

Japanese Patent Laid-Open No. 4-9121 JP 2007-143664 A Japanese Patent No. 40673320

  The first object of the present invention is to provide a tissue paper that has a smoothness and a moist feeling equivalent to or higher than those of conventional moisturizing tissue paper, and has reduced stickiness and tearability during use. The second problem of the present invention is that when storing the tissue paper, the storage box configured to be easy to take out, to maintain the ease of pop-up, and to be difficult to tear when taking out, is used. To provide tissue paper products.

The present invention that has solved the above problems is as follows.
<Invention of Claim 1>
A tissue paper product in which a two-ply tissue paper coated with a chemical on its surface is folded in a pop-up manner and stored in a substantially rectangular storage box,
The tissue paper has a drug content of 1.5 to 5.0 g / m ^{2 on} both sides,
The basis weight per layer of the sheet constituting 2 plies is 10 to 25 g / m ² ,
2-ply paper thickness is 100-140 μm,

The storage box is made of a paper box having an opening on the upper surface in parallel with the long side direction, the opening being covered with a film attached to the inner surface of the storage box, and the film is a slit parallel to the opening in the long side direction. Have
The thickness of the film is 33～38Myuemu, longitudinal bending resistance is Ri 0.8~1.4gf / 10mm der,
The slit is 45 to 65% of the length in the longitudinal direction of the web to be stored;
The pull-out direction when pulling out tissue paper from the storage box is configured to be the horizontal direction of tissue paper.
Tissue paper products characterized by that .

<Invention of Claim 2>
The tissue paper product of Claim 1 whose moisture content of the said chemical | medical solution is 1 to 15%.

<Invention of Claim 3>
The tissue paper product according to claim 1, wherein the dry tensile strength in the CD direction of the two plies of the tissue paper is 80 to 120 cN / 25 mm.

<Invention of Claim 4>
The tissue paper product according to claim 1, wherein a coefficient of static friction between sheets of the tissue paper is 0.50 to 0.65.

  By applying and infiltrating a chemical solution containing a predetermined amount of moisture into the sheet constituting the two-ply tissue paper, the crepe structure of the sheet is extended, and the tissue paper having a smooth surface is formed. Further, since the paper thickness is reduced and the fiber density is increased by the elongation, the strength between fibers is increased, and a tissue paper having a high tensile strength in the CD direction can be obtained. Whereas conventional moisturizing tissue applies a lotion solution to a thick base paper to create a film on the surface of the tissue to give the user smoothness, the present invention suppresses the thickness and the amount of solution applied, and provides a crepe structure. The surface is made smooth by stretching, thereby providing a smoothness higher than that of a conventional moisturizing tissue. In other words, the sticky feeling is reduced as a minimum amount of the lotion solution film on the tissue surface to make it feel smooth. Therefore, the drug content in the dry state is lower than that of conventional lotion type tissue paper, and it contains a sufficient amount of drug to exert its effect even though it does not easily cause stickiness when used. Therefore, it has enough moist and moisturizing properties. Furthermore, since the paper thickness is thin, it has a soft feeling in use as compared with the drug content.

  By using a multi-stand type interfolder, the manufacturing speed can be increased. When the multi-stand type interfolder is used, the manufactured tissue paper product has a form in which the consumer pulls out the tissue paper in the CD direction. However, the conventional moisturizing tissue does not have high paper strength, particularly the tensile strength in the CD direction, as compared to the non-humidifying tissue, so that a product manufactured by a multi-stand type interfolder is easily broken when pulled out. A problem is assumed.

  In the tissue paper product according to the present invention, as described above, the tissue paper has a strong tensile strength in the CD direction and a small coefficient of static friction, and is flexible as a tissue paper storage box on the film around the outlet. Is used, and the size of the outlet is specified. Thereby, even if the tissue paper is pulled in the CD direction and taken out, it is difficult to break, and the uppermost layer is difficult to fall into the box from the take-out port. When folding with a multi-stand type interfolder for moisture-retaining tissue paper, a continuous sheet containing moisture is processed while applying a relatively high tensile force in the MD direction and applying pressure in the thickness direction. The web bulk can be kept lower than when using a folder. By this effect, it can be stored in a compact storage box frequently used for non-humidifying tissue paper products.

  As described above, the present invention provides a tissue paper having a moist and smooth texture equal to or higher than that of a conventional moisturizing tissue, having less stickiness than the conventional moisturizing tissue, and having a high tensile strength in the CD direction. Is. In addition, since tissue paper can be pulled out from the storage box in the CD direction, a chemical-coated tissue paper product that can be manufactured at high speed using a multi-stand type interfolder is provided. Furthermore, the chemical | medical solution application | coating tissue paper products accommodated in the compact type | mold storage box are provided.

It is a figure which shows the apparatus outline | summary of the ply process of the tissue paper of 1st Embodiment which concerns on this invention. It is the schematic which shows an example of a multi stand type inter folder, and has shown the state seen from the front. It is the schematic which shows an example of a multi stand type inter folder, and has shown the state seen from the side. It is the schematic which shows an example of a multi stand type inter folder, and has shown the state seen from the front. It is a longitudinal cross-sectional view of the folded tissue paper. It is a principal part expansion perspective view of the site | part regarding a folding plate. It is a principal part expansion perspective view which shows how to fold a secondary continuous sheet (tissue paper). It is a principal part expansion perspective view which shows how to fold a secondary continuous sheet (tissue paper). It is a principal part expansion perspective view which shows how to fold a secondary continuous sheet (tissue paper). It is a figure which shows a mode that the (a) tissue paper bundle | flux of 1st Embodiment is accommodated in the storage box. (B) It is a partially broken figure which shows a mode that the tissue paper accommodated in the storage box is taken out. It is a figure which shows the measuring method of the MMD value of tissue paper. It is a perspective view which shows an example of the tissue paper product which concerns on this invention. It is an inner surface development view of the storage box of the tissue paper product of FIG. It is a perspective view which shows the other example of the tissue paper product which concerns on this invention. It is an inner surface expanded view of the storage box of the tissue paper product of FIG.

Hereinafter, embodiments of the present invention will be described in detail.
[Example of structure]
The base paper of the tissue paper according to the present invention has a ply structure in which two thin papers (hereinafter also referred to as sheets) are laminated.

[Thin paper]
On the other hand, as the raw pulp of the thin paper (sheet) constituting the tissue paper according to the present invention, for example, mechanical pulp such as ground wood pulp (GP), pressure-rise ground wood pulp (PGW), thermomechanical pulp (TMP), etc. : Chemical pulps such as semi-chemical pulp (SCP), softwood high yield unbleached kraft pulp (HNKP), softwood bleached kraft pulp (NBKP), hardwood unbleached kraft pulp (LUKP), hardwood bleached kraft pulp (LBKP), etc .: deink Examples include waste paper pulp such as depulp (DIP) and waste pulp (WP). The raw material pulp can be used by selecting one kind or two or more kinds. Preferably, a chemical pulp containing no filler or foreign matter is preferred. Further, the raw material pulp may contain woody materials such as straw pulp, bamboo pulp, kenaf pulp, and herbs.

  In particular, the raw material pulp is preferably a blend of NBKP and LBKP. Waste paper pulp may be blended as appropriate, but in terms of texture and the like, it is preferably composed only of NBKP and LBKP. In this case, the blending ratio is NBKP: LBKP = 20: 80 to 80:20. In particular, NBKP: LBKP = 30: 70 to 60:40 is desirable.

  On the other hand, in papermaking raw materials, other fiber raw materials include polyethylene terephthalate, polybutylene terephthalate, and polyester fibers such as copolymers thereof, polyolefin fibers such as polyethylene, polypropylene, and polystyrene, acrylics such as polyacrylonitrile and modacrylic. Fiber, polyamide fiber such as nylon 6, nylon 66, nylon 12, etc., synthetic fiber such as polyvinyl alcohol fiber, polyvinylidene chloride fiber, polyvinyl chloride fiber, urethane fiber, semi-synthetic fiber such as triacetate fiber, diacetate fiber, screw Include regenerated cellulose fiber such as coarse rayon, copper ammonia rayon, polynosic rayon, lyocell, and chemical fiber such as regenerated fiber spun from solution of collagen, alginic acid, chitin, etc. It is possible. The polymer constituting the chemical fiber may be in the form of a homopolymer, a modified polymer, a blend, a copolymer or the like.

  Raw materials such as pulp fibers are used as a base paper through, for example, a known papermaking process, specifically, a wire part, a press part, a dryer part, a calendar part, and the like. In this papermaking, for example, a dry paper strength enhancer, a wet paper strength enhancer, a softener, a release agent, a coating agent, a viscosity agent (knurl), a pH adjuster such as caustic soda, an antifoaming agent, a dye, etc. Chemicals can be added.

[US tsubo]
The rice paper weight per sheet of the tissue paper according to the present invention is preferably 10 to 25 g / m ² , more preferably 11 to 16 g / m ² . If the rice tsubo is less than 10 g / m ² , it is preferable from the viewpoint of improving softness, but it is difficult to ensure adequate strength that can withstand use. On the other hand, when the rice tsubo exceeds 25 g / m ² , the entire paper becomes hard, and a feeling of stickiness is generated, resulting in poor touch. In addition, the US tsubo is based on the US tsubo measurement method of JIS P 8124 (1998).

[Crepe rate]
The crepe rate of the primary raw sheet constituting the tissue paper of the present invention is 10 to 30%, more preferably 13 to 20%. Here, the crepe rate is expressed by the following equation.
Crepe rate: {(peripheral speed of the dryer during papermaking)-(peripheral speed of the reel)} / (peripheral speed of the dryer during papermaking) × 100.

[Medical solution]
Tissue paper of the present invention, the drug combined duplex 1.5~5.0g / m ^2, more preferably 3.0~5.0g / m ² containing. If the drug content is less than 1.5 g / m ² , the effect of the drug is not exhibited, and if it exceeds 5.0 g / m ² , the tissue paper has a sticky feeling, and the dry tensile strength decreases.

  About the chemical | medical solution to apply | coat, it is preferable that a viscosity shall be 1-700 mPa * s at 40 degreeC from a viewpoint of performing high-speed processing, especially 50-400 mPa * s. If it is less than 1 mPa · s, the chemical solution is likely to scatter on rolls such as anilox roll, printing plate roll, and gravure roll, and conversely if it is greater than 700 mPa · s, it is difficult to control the amount of application to each roll or continuous sheet. Ingredients include 70-90% polyol, 1-15% moisture, and 0.01-22% functional chemicals. The water content of the chemical solution to be applied was determined by the Karl Fischer method.

  Polyols include polyhydric alcohols such as glycerin, diglycerin, propylene glycol, 1,3-butylene glycol, polyethylene glycol, and derivatives thereof, and sugars such as sorbitol, glucose, xylitol, maltose, maltitol, mannitol, and trehalose.

  Functional agents include softeners, surfactants, inorganic and organic fine particle powders, oily components, and the like. Softeners and surfactants have the effect of imparting flexibility to the tissue and smoothing the surface, and anionic surfactants, cationic surfactants and zwitterionic surfactants are applied. Inorganic and organic fine particle powders have a smooth surface. The oil component has a function of improving lubricity, and higher alcohols such as liquid paraffin, cetanol, stearyl alcohol, and oleyl alcohol can be used.

  In addition, as a functional agent, one of a hydrophilic polymer gelling agent, collagen, hydrolyzed collagen, hydrolyzed keratin, hydrolyzed silk, hyaluronic acid or a salt thereof, ceramide, etc. A moisturizing agent such as any combination can be added.

  Deodorants such as flavors, emollients such as various natural extracts, vitamins, emulsifiers that stabilize compounding ingredients, antifoaming agents, antifungal agents, organic acids, etc. An agent can be appropriately blended. Furthermore, you may contain the antioxidant of vitamin C and vitamin E.

Of the above components, it is preferable to use a polyhydric alcohol such as glycerin or propylene glycol as a main component in order to stabilize the viscosity and coating amount of the chemical solution.
The temperature at the time of chemical solution application is preferably 30 ° C to 60 ° C, preferably 35 ° C to 55 ° C.

[Amount of application]
The coating amount was calculated from the difference between each sheet basis weight when the chemical solution after ply was not applied during operation and each sheet basis weight immediately after the corresponding application.
(Coating amount g / m ²⁾ = (basis weight g / m ² immediately after coating) - (the basis weight g / m ² in the case of not applying)
The coating amount of both surface layers or the total coating amount of both surfaces is the total coating amount per unit area of the plyed tissue paper sheet, and the coating amount of each sheet is added.

[Drug content]
The drug content refers to the content of the drug component in a dry state (absolutely dry) contained in the unit area of tissue paper in the standard state of JIS P 8111 (1998). Specifically, in the applied chemical solution The content of components other than moisture shall be indicated. The unit area of the tissue paper is an area of the plyed sheet viewed from a viewpoint perpendicular to the plane, and does not mean the total area of each plyed sheet and its front and back surfaces.

[Drug content]
The chemical content is defined as a tissue paper product having a predetermined mass conditioned under JIS P 8111 (1998) as a denominator (A) (g), and the water content in the chemical solution contained in the tissue paper product having a predetermined mass. The ratio of (B) divided by (A) is expressed as (%), with the removed mass (B) (g) as a molecule.
(Drug content%) = (B) ÷ (A) × 100 (%)

[Drug density]
The chemical solution density is the drug content per volume of two-ply tissue paper in the standard state of JIS P 8111 (1998).

[Paper thickness]
The paper thickness of the tissue paper according to the present invention is 100 to 140 μm, more preferably 120 to 140 μm in a 2-ply state. If the paper thickness is less than 100 μm, it is preferable from the viewpoint of improving the softness, but it is difficult to ensure adequate strength as tissue paper. On the other hand, when the thickness exceeds 140 μm, the texture of the tissue paper is deteriorated and a feeling of tingling is generated during use.

  As a method for measuring the paper thickness, the specimen is fully conditioned under the conditions of JIS P 8111 (1998), and then the dial thickness gauge (thickness measuring instrument) “PEACOCK G type” (manufactured by Ozaki Seisakusho) under the same conditions. It shall be measured in the state of 2 plies using. Specifically, confirm that there is no dust, dust, etc. between the plunger and the measuring table, lower the plunger on the measuring table, move the memory of the dial thickness gauge to adjust the zero point, and then Raise the plunger, place the sample on the test bench, slowly lower the plunger and read the gauge at that time. At this time, only the plunger is placed. The terminal of the plunger is made of metal so that a circular plane having a diameter of 10 mm is perpendicular to the plane of the paper, and the load at the time of measuring the paper thickness is about 70 gf. The paper thickness is an average value obtained by performing measurement 10 times.

[Tensile strength]
The tensile strength of the tissue paper according to the present invention is measured in a two-ply state.
The dry tensile strength is measured according to the tensile test method of JIS P 8113 (1998). Among them, it is cut into a width of 25 mm in the vertical direction and the horizontal direction under the standard conditions defined in JIS P 8111 (1998).

  The dry tensile strength of the tissue paper according to the present invention is 180 to 350 cN / 25 mm in the MD direction, more preferably 160 to 300 cN / 25 mm, 80 to 120 cN / 25 mm in the CD direction, and more preferably 80 to 110 cN / 25 mm. The ratio of the direction / CD direction is preferably 1.5 to 3.0.

  The wet tensile strength is determined according to JIS P 8135 (1998). The wet tensile strength of the tissue paper is 70 to 160 cN / 25 mm in the MD direction, more preferably 80 to 130 cN / 25 mm, and 33 to 50 cN / 25 mm, more preferably 35 to 45 cN / 25 mm in the CD direction.

[Softness]
The softness value of the tissue paper of the present invention is preferably 0.80 to 1.10 cN / 100 mm. The softness here is measured based on the handle ohm method according to the JIS L 1096 E method.
However, the test piece was 100 mm × 100 mm in size, and the clearance was 5 mm. The measurement was performed 5 times each in the longitudinal direction and the lateral direction with 1 ply, and the average value of all 10 times was represented by 2 digits of decimal point and expressed in units of cN / 100 mm.

  By setting the softness within the above range, it is possible to reduce the resistance value when taking out the tissue paper to make it difficult to break, and to balance the feeling of thickness and softness.

〔Moisture percentage〕
The moisture content of the product is desirably 10.0 to 13.0%. The moisture content is determined based on JIS P 8127.
Moisture content (%) = {(weight of paper before drying) − (weight of paper after drying)} / (weight of paper before drying) × 100

〔Growth rate〕
The elongation in the MD direction of the product is desirably 11.0 to 15.0%. The elongation rate here is measured using “Universal Tensile Compression Tester TG-200N” manufactured by Minebea Co., Ltd. The elongation is the “stretch at break” described in “3. Definition e)” of JIS P8113.

[Static friction coefficient]
On the other hand, the tissue paper of the present invention desirably has a coefficient of static friction between tissue papers of 0.50 to 0.65, more preferably 0.55 to 0.60. The static friction coefficient here is measured by the following method according to JIS P 8147 (1998).
The tissue paper peeled off in one ply is attached to the acrylic plate so that the outer surface of the tissue paper is on the outside. Wrap tissue paper around a 100 g weight with 2 plies and place it on the tissue on the acrylic plate. Tilt the acrylic plate and measure the angle at which the weight slides down. Angle measurement is carried out 10 times in total, 5 times for each of the tissue in the vertical and vertical directions (MD and MD directions), and in the horizontal and horizontal directions (CD and CD directions), and the average angle is calculated. The tangent value is defined as a coefficient of static friction.

  The following can be considered as a principle for reducing the static friction coefficient. In the present invention, two primary raw fabric continuous sheets are plyed, the crepe peak is smoothed by calendering, the sheet surface is smoothed by smoothing the crepe peak, and then the lotion chemical solution Is preferably applied by a transfer method. The applied secondary raw sheet is stored under a certain tension and seasoned until it is folded. During this time, the lotion chemical solution spreads over time so as to be uniform inside the paper layer in a planar and thickness direction. In the subsequent process, when folding by the multi-stand type interfolder is performed, the secondary continuous sheet is pulled out from the ply raw fabric, folded, and cut through a process of pressing with a pull conveyor while pulling. In this folding process, folding processing is started in a state in which it is coated and seasoned and moisture is absorbed in the paper layer. Due to seasoning and subsequent tension and pressure in the thickness direction, unevenness due to creping on the sheet surface is reduced, and friction between sheets is reduced.

[MMD]
MMD is an average deviation (unit: dimensionless) of the friction coefficient μ. MMD is one of the indices of smoothness. The smaller the numerical value, the smoother, and the larger the numerical value, the less smooth.
As a method for measuring the MMD value, as shown in FIG. 11A, a tension of 20 g / cm is applied to the contact surface of the friction element 112 in a predetermined direction (downward and rightward in FIG. 11A). While being brought into contact with the surface of the tissue paper 111, which is the measurement sample, at a contact pressure of 25 g, it is moved 2 cm at a speed of 0.1 cm / s in the same direction as the direction in which the tension is applied. At this time, the friction coefficient was measured using a friction tester KES-SE (manufactured by Kato Tech Co., Ltd.), and the average deviation of the friction coefficient μ at a friction distance of 2 cm (moving distance was 3 cm and excluding 5 mm before and after each). Was defined as the MMD value.
The friction element 112 has 20 piano wires P with a diameter of 0.5 mm adjacent to each other, and has a contact surface formed so that the length and width are both 10 mm. The contact surface is formed with a unit bulging portion whose tip is formed of 20 piano wires P (curvature radius 0.25 mm).
FIG. 11A schematically shows the friction element 112, and FIG. 11B shows an enlarged view of a portion surrounded by an alternate long and short dash line in FIG. 11A.

[Web bulk]
A plastic plate having a weight of 30 g and a size of 130 mm × 250 mm was placed on the tissue paper bundle, and the heights of the four corners were averaged to obtain the web bulk value.
The web volume of the tissue paper according to the present invention is 0.25 to 0.40 mm per set. In particular, it is preferably 0.28 to 0.36 mm per set and 55 to 65 mm for 180 sets. If the web bulk is too low, it becomes difficult for the user to put the finger deeply out of the take-out opening when taking out the uppermost tissue from the storage box, making it difficult to take out. Further, if the web bulk is too high, it cannot be stored in a compact storage box (having a box height of about 55 to 65 mm), and manufacturing costs and transportation costs are increased, or the web is compressed during storage and is compact. In order to store in the storage box, the top layer must be pulled out with a strong force when taking out, and there is a problem that the tissue paper is easily torn.

[Product density]
The tissue paper according to the present invention is folded by an interfolder or the like, and is cut into a product size at any stage before or after the folding process. For example, 180 sets are packed into a product. The paper density after 180 sets of folding is preferably 0.15 to 0.25 g / cm ³ , more preferably 0.17 to 0.23 g / m ³ . If it is lower than 0.15 g / cm ³ , moist feeling and smoothness cannot be obtained, and if it is higher than 0.25 g / cm ³ , the thickness of the tissue paper is impaired and a sticky feeling is produced, and the water absorption is deteriorated. End up.
The product density is the paper thickness (D) of tissue paper (2 ply) according to “PEACOCK G type”, which is a double value (C) of the tissue paper product tsubo conditioned under JIS P 8111 conditions. The unit is expressed in g / cm ³ and 3 decimal places.
((Density (g / cm ³ )) = (C (g / m ² )) × 2 ÷ (D (μm))

[Storage box]
12 shows a tissue paper product according to the present invention, and FIG. 13 shows a view of the storage box 201 as seen from the inside of the box in the unfolded state. As a material for forming the box, any known material used as a tissue paper storage box such as cardboard having a basis weight of 300 to 450 g / m ² can be used. The tissue paper storage box 201 has a rectangular parallelepiped shape in an assembled state as shown in FIG. 12, and includes a pair of upper and lower upper surfaces 202 and 203, a pair of front and rear front surfaces 204 and 205, and a pair of left and right left sides. A surface 204 and a right side 205. In this case, the front and rear surfaces 204 and 205 and the left and right side surfaces 206 and 207 correspond to the peripheral surface of the present invention.

  As can be seen from the developed state of FIG. 13, the adhesive margin piece 203b extends from the rear edge of the lower surface (the edge adjacent to the rear surface of the peripheral edge) over the entire long side, and the adhesive margin piece 203b overlaps the inner side of the rear surface. Then, a cylindrical portion composed of the upper surface 202, the lower surface 203, the front surface 204, and the rear surface 205 is formed by being bonded and fixed by an adhesive such as a hot melt adhesive.

  The left and right side surfaces 204 and 205 extend from an adjacent edge of the upper surface 202 and an adjacent edge of the lower surface 203, respectively, and from an adjacent edge of the front surface 204 and an adjacent edge of the rear surface 205, respectively. The front flap 204f and the rear flap 205f, the upper flap 202f and the lower flap 203f are overlapped on the outside of the front flap 204f and the rear flap 205f, and the upper flap 202f and the lower flap 203f are the front flap and the rear flap 205f. The lower end portion of the upper flap 202f is overlapped on the outer side of the upper end portion of the lower flap 203f, and the overlapped portion is fixed by the adhesive.

  The inner dimension of the box is preferably 5 to 20 mm, particularly 8 to 15 mm longer than the length in the longitudinal direction of the web to be stored. By providing a gap in the longitudinal direction inside the storage box, it becomes possible to take out the tissue paper with almost no resistance between the inner surface of the box and the tissue paper.

  The height of the storage box can be arbitrarily determined within the scope of the present invention in accordance with the number of web sets to be stored, but considering the economic efficiency and convenience of use, the number of web sets is set to 150 to 300 sets. The height of the storage box is preferably 50 to 120 mm.

  Furthermore, the height of the storage box is preferably 50 to 80 mm, more preferably 55 to 65 mm, in order to reduce manufacturing costs and transportation costs.

  A cutout such as a perforation is formed in advance on the upper surface 202 of the storage box 201, and an extraction window (opening) 202a is formed by peeling off the lid portion 202b surrounded by the cutout at the start of use. It has become. As shown in FIGS. 14 and 15, the lid portion 202 b may be configured so as to be a valley fold line 202 g without being cut off at substantially one side. By setting it as such a structure, the cover part 2b can be utilized as a cover of the extraction window 202a. Alternatively, the take-out window 202a may be opened in advance and the lid portion 202b may not be provided. The length in the long side direction of the take-out window 202a is 50 to 70%, particularly 55 to 65% of the length in the longitudinal direction of the web to be stored. The length in the short side direction of the take-out window 202a is preferably 35 to 55%, particularly 40 to 50% of the length in the short side direction of the web.

  A film-like cover sheet 202c is attached to the take-out window 202a from the inside of the box with a hot-melt adhesive or the like, and a portion of the cover sheet 202c surrounded by the take-out window 202a has a long side direction of the box 1 A slit 202s is formed. The slit 202s is 45 to 65%, particularly 50 to 60% of the length in the longitudinal direction of the web to be stored. The slit 202s is particularly preferably arranged in the vicinity of the center of the extraction window 202a in both the long side direction and the short side direction.

  As a material for forming the cover sheet, a resin film sheet made of a resin such as polyethylene, polypropylene, polyester, or a laminated resin film sheet obtained by laminating these, a laminated film sheet laminated with a film sheet and a thin paper, etc. Examples include synthetic paper sheets made of fibers. A resin film sheet is preferable in consideration of the take-out property, and a low-density polyethylene film (LDPE) that is particularly flexible and low in production cost can be suitably used.

  The thickness of the film is desirably 33 to 38 μm. Further, it is preferable that the longitudinal bending resistance of the film is 0.8 to 1.4 gf / 10 mm, particularly 1.0 to 1.2 gf / 10 mm. The bending resistance was measured based on the handle ohmmeter method described in JIS L 1096 E method. The test piece was 100 mm long × 10 mm wide, and the clearance was 5 mm. The average value of 10 times in 1 ply in the vertical direction was represented by 2 digits of decimal point and expressed in units of cN / 100 mm. The longitudinal direction of the film coincides with the slit direction of the film. If the bending resistance of the film in the longitudinal direction is higher than 1.4 gf / 10 mm, it will be easy to tear when taking out the tissue paper, and if it is lower than 0.8 gf / 10 mm, it will be difficult to hold the tissue paper in the outlet and pop-up will occur. It becomes difficult.

  Furthermore, the coefficient of static friction between the lateral direction of the film and the tissue paper (the removal direction) is 0.20 to 0.30, more preferably 0.23 to 0, in order to improve the slip of the tissue paper at the time of taking out and suppress the resistance. .28. The film transverse direction means a direction perpendicular to the film longitudinal direction and the film plane. The coefficient of static friction between the film and tissue paper was measured by the following method. The film is affixed to the acrylic plate so that the slope direction is the lateral direction of the film so that the inner surface of the storage box is on the outside. Wrap tissue paper around a 100 g weight with 2 plies, and place it on the film on the acrylic plate so that the slope direction is the tissue removal direction. Tilt the acrylic plate and measure the angle at which the weight slides down. The angle measurement was performed 10 times, the average angle was calculated, and the tangent value was taken as the static friction coefficient.

[Tissue paper removal resistance]
By setting the resistance applied when taking out the tissue paper within a certain range, it is possible to minimize tearing during the taking out. The tissue paper take-out resistance is measured by the following method. Secure the center tip of tissue paper to the gauge tip of the pushbull gauge, and take the tissue paper vertically from the storage box with the bottom surface fixed at a constant speed over a period of 0.4 to 0.6 seconds. The resistance value was measured. The tissue paper to be taken out is a total of 5 sets from the first set to the 5th set from the top layer, and a total of 5 sets from the 11th set to the 15th set. It was. The take-out resistance is preferably 70 gf or less, more preferably 50 to 70 gf.

[Example of manufacturing method]
The tissue paper of the present invention described above can be manufactured as follows. In FIG. 1, the outline | summary of the apparatus of the ply process of the tissue paper which concerns on this invention was shown. In addition, it is preferable to implement the process which concerns on FIG. 1 with the ply machine which is an apparatus integrated with the coating device (on-machine coating).

  The base paper produced by the paper machine is creped as a continuous sheet, calendered, and wound up to form primary rolls 11 and 12 (generally also called jumbo rolls). The

  The continuous sheets 31 and 32 are laminated by the laminating roller 13 to form two plies, and if necessary, calendered by the ply machine calendar 14 and sent to the chemical solution coating process. Any known coating method such as dipping, spraying, flexo coating, and gravure coating can be used as the chemical coating method, but printing methods such as gravure coating and flexographic coating that perform chemical coating evenly on the entire coated surface In particular, it is more preferable to use a flexo coater equipped with a doctor chamber 15 because a chemical solution can be supplied in a stable coating amount.

  In the ply process of FIG. 1, two flexo coaters 16 and 17 are provided, and a chemical solution is applied to each surface of a two-ply continuous sheet.

  When the flexographic printing method is used as the chemical solution applying means, the processing speed is 100 to 1100 m / min, preferably 350 to 1050 m / min, particularly preferably 450 to 1000 m / min. If it is less than 100 m / min, the productivity is low, and if it is more than 1100 m / min, uneven coating occurs and the chemical solution is likely to scatter. The number of lines of the flexographic printing plate roll is 10 to 60 lines, preferably 15 to 40 lines, and particularly preferably 20 to 35 lines. If the number of lines is less than 10, many coating irregularities occur. On the other hand, if the number of lines exceeds 60 lines, the paper dust tends to clog. The number of lines of anilox roll is 10 to 300 lines, preferably 25 to 200 lines, particularly preferably 50 to 100 lines. If the number of lines is less than 10, many coating irregularities occur. On the other hand, if the number of lines exceeds 300 lines, the paper dust tends to be clogged. The anilox roll has a cell capacity of 10 to 100 cc, preferably 15 to 70 cc, particularly preferably 30 to 60 cc. If the cell capacity is less than 10 cc, a desired coating amount cannot be obtained. On the other hand, if the cell capacity is more than 100 cc, the amount of chemical solution scattered increases. By setting it as such a structure, a chemical | medical solution is transcribe | transferred to the crepe peak part of a continuous sheet in the shape of a dot of 1 mm or less, and a uniform application | coating sheet is obtained.

The flexographic printing method can stabilize the coating amount even when the processing speed is high, and can stably apply a wide range of chemical viscosity with a single roll.
When the gravure printing method is used as the chemical solution applying means, the processing speed is 100 to 1000 m / min, preferably 350 to 950 m / min, particularly preferably 450 to 950 m / min. When it is less than 100 m / min, productivity is low, and when it is more than 1000 m / min, coating unevenness occurs and the chemical solution is likely to be scattered. The number of gravure rolls is 40 to 160 lines, preferably 60 to 140 lines, particularly preferably 80 to 120 lines. If the number of lines is less than 40 lines, the amount of chemical solution scattered increases, whereas if the number of lines exceeds 160 lines, paper dust tends to be clogged.

  When the chemical spraying method is used as the chemical coating means, the spraying means is not particularly limited, but may be a nozzle dampening method or a rotor dampening spraying method. The processing speed is 100 to 1100 m / min, preferably 350 to 1050 m / min, and more preferably 450 to 1000 m / min.

  The sheet after application of the chemical solution is supplied to a contact embossing roller 18 and a roller roll 19 and fixed by subjecting a two-ply continuous sheet to a contact embossing (knurling) process. At this time, the continuous sheet 32 with a small amount of chemical solution applied is disposed so as to contact the contact embossing roller 18. The contact embossing is preferably applied uniformly in the vertical direction with a width of 1 to 10 mm at positions of 1/10 to 1/20 with respect to the paper width from both sides. Any of the known methods such as fixing the ply with an adhesive may be used. However, when using an adhesive, there is a problem that the touch tends to become hard, and it is easy to peel off when applying a chemical solution. It can be said that the use of embossing is more preferable.

2 ply continuous sheet with contact embossing is cut directly into product size after being subjected to folding processing by being directly applied to a rotary interfolder or the like, or after being cut into product width by slitter 20, The winding roll 21 makes a take-up secondary raw roll 22 which is folded and stored in a paper box.
In this embodiment, the chemical solution is applied before the contact embossing. However, the chemical solution may be applied after the contact embossing.

  Chemical solution application may be performed either on-machine or off-machine. Further, the chemical solution applying means may be provided before the winding process of the primary continuous sheet of the paper machine (if the calendar process is performed, it may be before or after the calendar process) or before the interfolder is folded. Furthermore, the chemical solution application means is not limited to a single one, and may be configured to apply the chemical solution in a plurality of steps.

[Multi-stand type inter folder]
The secondary raw roll described above is subjected to a folding process particularly in tissue paper products. As the folding process, a known method such as a rotary interfolder or a multi-stand interfolder can be used, but it is more preferable to use a multi-stand interfolder with high productivity. In the present invention, as described above, it is necessary to use a multi-stand type interfolder because the static friction coefficient of tissue paper needs to be low and the web bulk needs to be low.

  A large number of secondary web rolls 22 are set in a multi-stand type interfolder, and a tissue paper bundle is manufactured by drawing out a secondary continuous sheet from the set secondary web roll 22 and folding and stacking them. Hereinafter, an example of the multi-stand type interfolder will be described.

  2 and 3 show an example of a multi-stand type interfolder. Reference numeral 2 in the drawing denotes secondary raw rolls 22, 22... Set on secondary raw roll support portions (not shown) of the multi-stand type interfolder 1. These secondary raw rolls 22, 22... Are set side by side in the direction (the horizontal direction in FIG. 2, the front-to-back direction in FIG. 3) in which the required number is orthogonal to the illustrated plane. Each secondary raw roll R has slits in the width of tissue paper product in the above-described manufacturing equipment and manufacturing method of the secondary raw roll for tissue paper products. It is wound and set in double width.

  The continuous belt-like secondary continuous sheets 63A and 63B unwound from the secondary raw roll 22 are guided by guide means such as guide rollers G1 and G1 and fed into the folding mechanism section 60. Moreover, the folding mechanism part 60 is provided with the folding plate group 64 in which the required number of folding plates P, P ... are arranged in parallel as shown in FIG. For each folded plate P, guide rollers G2, G2 and guide round bar members G3, G3 for guiding a pair of continuous secondary continuous sheets 63A or 63B are respectively provided at appropriate positions. Further, below the folded plates P, P..., A conveyor 65 is provided that receives and conveys the laminated band 67 that is stacked while being folded.

  A folding mechanism using this type of folded plates P, P... Is a known mechanism, for example, from US Pat. As shown in FIG. 5, this type of folding mechanism folds each continuous secondary continuous sheet 63A, 63B... In the Z-shape and is adjacent to the adjacent secondary continuous sheets 63A, 63B. Stack the ends together.

  FIGS. 6 to 9 show in detail the portions of the folding mechanism 60 that are particularly related to the folded plate P. FIG. In the folding mechanism 60, a pair of continuous secondary continuous sheets 63A and 63B are guided for each folded plate P. At this time, the continuous secondary continuous sheets 63A and 63B are guided by the guide round bar members G3 and G3 while being shifted in position so that the side end portions do not overlap each other.

  The continuous secondary continuous sheet that overlaps the lower side when guided by the folded plate P is the first continuous secondary continuous sheet 63A, and the continuous secondary continuous sheet that overlaps the upper side is the second continuous sheet. As shown in FIGS. 5 and 7, these continuous secondary sheets 63A and 63B are second continuous secondary continuous sheets of the first continuous secondary continuous sheet 63A. The side end e1 that does not overlap the sheet 63B is folded back to the upper side of the second continuous secondary continuous sheet 63B by the side plate P1 of the folded plate P, and as shown in FIG. 5 and FIG. The side end portion e2 of the continuous secondary continuous sheet 63B that does not overlap the first continuous secondary continuous sheet 63A is folded downward so as to be drawn under the folded plate P from the slit P2 of the folded plate P. . At this time, as shown in FIGS. 5 and 9, the side end e3 (e1) of the continuous secondary continuous sheet 63A stacked while being folded in the upstream folded plate P is second from the slit P2 of the folded plate P. Are guided between the folded portions of the secondary continuous sheet 63B. In this way, each continuous secondary continuous sheet 63A, 63B... Is folded in a Z shape and the side ends of adjacent continuous secondary continuous sheets 63A and 63B are crossed together, so that the product is used. In some cases, when the top tissue paper is pulled out, the side edge of the next tissue paper is pulled out.

  As shown in FIG. 2, the laminated band 70 obtained in the multi-stand type interfolder 6 as described above is cut (cut) at a predetermined interval in the flow direction FL by the cutting means 66 at the subsequent stage, and the tissue is cut. This tissue paper bundle 30a is further stored in the storage box B in the subsequent equipment as shown in FIG. 10 (a). In the multi-stand type interfolder 1 as described above, the paper direction of the laminated band 70 is the vertical direction (MD direction) along the flow direction FL, and the horizontal direction along the direction orthogonal to the flow direction. Direction (CD direction). For this reason, the direction of the paper of the tissue paper constituting the tissue paper bundle 67a obtained by cutting the laminated band 70 into a predetermined length is along the folding direction of the tissue paper as shown in FIG. The horizontal direction (CD direction) and the vertical direction (MD direction) along the direction orthogonal to the folding direction of the tissue paper.

  FIG. 10B shows an example of a product in which the tissue paper bundle 67a is stored in the storage box B. A perforation M is provided on the upper surface of the storage box B, and a part of the upper surface of the storage box B is broken by the perforation M so that the upper surface of the storage box B is opened. The opening is covered with a film F having a slit at the center, and the tissue paper T can be taken out through the slit provided in the film F.

  By the way, as described above, the direction of the paper of the tissue paper constituting the tissue paper bundle 67a is the horizontal direction (CD direction) along the folding direction of the tissue paper, as shown in FIG. When the tissue paper T is pulled out from the storage box B, the pulling direction is along the horizontal direction (CD direction) of the tissue paper T.

In order to confirm the effect of the present invention, Table 1 shows the results of evaluating the dimensions of the product and the paper quality of the tissue paper for the examples and comparative examples according to the present invention.
Examples 1 to 7 are tissue papers according to the present invention manufactured using a multi-stand type interfolder for folding.

  Comparative Examples 1 to 4 are commercially available products, Comparative Example 1 is a non-moisturizing general purpose tissue paper, and Comparative Examples 2 to 4 are moisturizing lotion type tissue papers.

  The composition of the chemical solution applied to Examples 1 to 7 was adjusted as shown in Table 2. The method for measuring tissue weight, paper thickness, tensile strength, elongation, softness, coefficient of static friction, moisture content, MMD, and tissue resistance of tissue paper is described in the section of the embodiment for carrying out the invention. Just as you did. The drug content indicates the ratio of the dry weight of the drug to the tissue paper basis weight.

  Table 1 shows the inner dimensions of the storage boxes for the tissue paper products of Examples 1 to 7 and Comparative Examples 1 to 4, the dimensions of the take-out window, the length of the slit, the material, thickness, and Clark stiffness of the film.

Along with the evaluation of paper quality, sensory evaluation based on the following criteria was performed for 10 people in Examples 1 to 7 and Comparative Examples 1 to 4 for softness, smoothness, thickness, and moist feeling. The sensory evaluation was performed on the basis of the following criteria, with all results of Comparative Example 1 being a non-humidifying tissue paper set to 3.
5: Very good 4: Excellent 3: Equivalent to the standard 2: Inferior 1: Notably inferior The tissue-coated tissue paper was also evaluated for the presence or absence of stickiness.
○: Little sticky feeling ×: Clearly sticky feeling
The ease of taking out the tissue paper was evaluated as follows by carrying out the taking out operation for 10 people.
○: Resistance at the time of taking out was small, and there was no tear.
Δ: 1 to 4 people broke or complained of difficulty in taking out due to resistance.
X: Five to ten people complained of tearing.
Regarding the presence or absence of the tissue paper in the storage box, for 10 people, all tissue paper products were taken out from the first set to determine whether or not there was any depression.
○: There was no depression.
Δ: 1 to 4 people experienced a drop once or more.
X: 5-10 people experienced the depression once or more.
The difficulty of tearing at the time of use was evaluated by using tissue paper as a nose for 10 persons and determining whether there was any tear.
○: 3 or fewer people were torn or not torn.
Δ: 4 to 8 people were torn.
X: 9 to 10 persons were torn.

The tissue paper according to the present invention showed high values of the dry tensile strength and the wet tensile strength in the CD direction as compared with a commercially available moisturizing tissue. The wet tensile strength in the CD direction was higher than that of conventional general-purpose tissue paper. It was also shown that the softness and static friction coefficient were lower than those of commercial products, and the paper was smooth and soft.
In sensory evaluation, the tissue paper according to the present invention is not excellent in thickness, but has a softness, smoothness, moist feeling equal to or higher than that of a moisturizing tissue, and a sticky feeling seen in a moisturizing tissue. I found out that it was alleviated.

  In particular, the following factors can be considered as factors that have good slipperiness for the tissue paper according to the present invention. Although it depends on the permeability of the chemical applied to tissue paper, when a chemical containing both hydrophilic and lipophilic components is applied, the hydrophilic components are absorbed into the pulp and the lipophilic components tend to remain on the paper surface. It is considered that surface friction is reduced. However, increasing the amount of chemical solution applied as in conventional moisturizing tissue, the hydrophilic component is not sufficiently absorbed into the pulp and remains on the surface, reducing the friction-reducing effect of the lipophilic component and hydrophilic components (such as glycerin). It is presumed that the slipperiness decreases due to the viscosity of.

In Examples 1 to 7, significantly better results than Comparative Examples 1 to 3 were obtained regarding the resistance to taking out tissue paper and the ease of taking out tissue paper. Thereby, it can be said that the risk of tearing at the time of taking out was reduced because slipping when taking out the tissue paper was good and the tissue paper could be taken out smoothly. In Comparative Example 4, there is a gap between the web and the inner surface of the upper portion of the box, and the web is softly inserted. Therefore, friction between the sheets hardly occurs, and the take-out resistance is small. However, the comparative example 4 has a problem that the sheet is likely to drop during use and is difficult to pop up. Compared with this, even if Example 1-4 improves sliding, it turns out that the tissue paper in use does not fall into the inside of a storage box from a slit part, and does not impair a usability even in the middle of use. It was.
Moreover, in Comparative Examples 2-4, it turned out that the tear at the time of use tends to arise, but Examples 1-7 are hard to produce a tear.

  As described above, the tissue paper according to the present invention has a sticky feeling seen in conventional moisturizing tissue and has a softness, smoothness, and moist feeling equivalent to or higher than that of the moisturizing tissue. It turned out to be. Further, it was found that the tissue paper can be taken out smoothly and is not easily torn at the time of taking out.

  The tissue paper and tissue paper product of the present invention can be used for tissue paper and tissue paper products used for wiping applications, in particular, body wiping applications, and facial applications.

  The present invention relates to tissue paper and tissue paper products.

The tissue paper in the domestic market is broadly divided into non-moisturizing tissue and moisturizing tissue. Here, the moisturizing tissue is a tissue produced by applying a moisturizing agent such as glycerin to a tissue base paper that has been made, and the non-humidifying tissue is a general tissue that does not apply a moisturizing agent to the tissue base paper.
The use of tissue paper is mainly for personal use, mainly for facial use including nasal cover, and moisturizing tissue is considered to be a product specification specialized for nasal blow.
In the past, tissue paper has been used for facial applications, mainly for nasal clasps, and so many attempts have been made so far in order to pursue good touch and quality improvements have been repeated. For example, various softeners are added to the raw materials to improve the flexibility of the product. Many supple fibers with low fiber roughness are used. Fine creping by sticking when wet paper dryer is dried and adjusting per doctor. The softness and smoothness of the paper is achieved by technologies such as forming the surface, improving the surface properties by a calender, and adjusting the raw material beating rate to a low level while maintaining the lateral strength by adjusting the ratio of the web speed. Improvements have been made.

However, in order to further improve quality, non-moisturizing tissue has technical limitations and an increase in the number of people suffering from hay fever and allergic rhinitis has led to the development of moisturizing tissue that is now part of the tissue market. Accounted for.
Heavy users, such as allergic rhinitis and hay fever, bite their nose more than tens of times a day, and the nose and its surroundings are rubbed against tissue, causing mild inflammation and redness. Therefore, for such a user, a material having a small friction on the tissue surface, that is, a material having smoothness is preferably used. The moisturizing tissue applies an aqueous lotion solution containing a hygroscopic moisturizing agent such as glycerin to the base paper of the sanitary thin paper. Glycerin is less irritating to the skin as used in cosmetics, absorbs moisture and moistens and softens the tissue, forms a thin film on the surface of the tissue, and is clearly softer than ordinary non-applied tissue It is recognized as a differentiated product with a smooth touch. For example, a technique for externally applying an oily substance and a humectant has been introduced (Patent Document 1).

  In this way, moisturizing tissue is recognized and consumption is increasing, but some moisturizing tissue heavy users leave moisturizers on their skin after biting their nose and feel sticky, and some dislike this Exists. Regarding this sticky feeling, a method for improving the sticky feeling by changing the chemical composition such as blending organic and inorganic powders as in Patent Document 2 is also known.

  Conventionally, in the manufacture of moisturizing tissue, it is common to apply chemicals off-machine after the paper making process and the plying process, and then perform folding using a rotary interfolder, which is often used for manufacturing non-humidifying tissue. No multi-stand interfolder is manufactured.

  As a box tissue product, it is the mainstream to use a storage box (height of about 50 to 65 mm) that is reduced in height and reduced in size from the viewpoint of reducing the manufacturing cost and transportation cost of the box. When using a compact storage box, the tissue paper stored inside is usually compressed, and the outlet on the top of the storage box is used to eliminate the difficulty of removing the top layer of tissue paper due to compression. It is designed to be longer than the long side direction of the upper surface (Patent Document 3). However, in the moisturizing tissue, there is a problem that the tissue paper is difficult to be held in the take-out port due to its high slipperiness and falls into the storage box, making it difficult to pop up. On the other hand, in order to hold tissue paper in the take-out port, when taking measures such as reducing the take-out port and increasing the rigidity of the film arranged in the take-out port, there is a problem that it is easily broken when taking out the tissue paper. Can occur.

Japanese Patent Laid-Open No. 4-9121 JP 2007-143664 A Japanese Patent No. 40673320

  The first object of the present invention is to provide a tissue paper that has a smoothness and a moist feeling equivalent to or higher than those of conventional moisturizing tissue paper, and has reduced stickiness and tearability during use. The second problem of the present invention is that when storing the tissue paper, the storage box configured to be easy to take out, to maintain the ease of pop-up, and to be difficult to tear when taking out, is used. To provide tissue paper products.

The present invention that has solved the above problems is as follows.
<Invention of Claim 1>
A tissue paper product in which a two-ply tissue paper coated with a chemical on its surface is folded in a pop-up manner and stored in a substantially rectangular storage box,
The tissue paper has a drug content of 1.5 to 5.0 g / m ^{2 on} both sides,
The basis weight per layer of the sheet constituting 2 plies is 10 to 25 g / m ² ,
2-ply paper thickness is 100-140 μm,
The storage box is made of a paper box having an opening on the upper surface in parallel with the long side direction, the opening being covered with a film attached to the inner surface of the storage box, and the film is a slit parallel to the opening in the long side direction. Have
The film has a thickness of 33 to 38 μm and a longitudinal bending resistance of 0.8 to 1.4 gf / 10 mm.
The slit is 45 to 65% of the length in the longitudinal direction of the web to be stored;
Withdrawing direction when pulling out the tissue paper from the storage box is configured such that the lateral tissue paper,
A tissue paper product characterized in that the extraction resistance value of a total of 5 sets from the 1st set to the 5th set from the top layer and a total of 5 sets from the 11th set to the 15th set is 70 gf or less .

<Invention of Claim 2>
The tissue paper product of Claim 1 whose moisture content of the said chemical | medical solution is 1 to 15%.

<Invention of Claim 3>
The tissue paper product according to claim 1, wherein the dry tensile strength in the CD direction of the two plies of the tissue paper is 80 to 120 cN / 25 mm.

<Invention of Claim 4>
The tissue paper product of Claim 1 whose static friction coefficient measured by the procedure of following (A)-(D) is 0.50-0.65 .
(A) The tissue paper is peeled off in one ply and attached to the acrylic plate so that the surface that was on the outer surface of the tissue paper at the time of two plies becomes the outside.
(B) A tissue paper different from the tissue paper is wound around a 100 g weight with 2 plies and placed on the tissue paper on the acrylic plate.
(C) Tilt the acrylic plate and measure the angle at which the weight slides down.
(D) The angle is measured in the vertical direction of tissue paper (MD direction and MD direction) and in the horizontal direction of tissue paper (CD direction and CD direction), and measurement is performed 10 times, 5 times each. Then, the average angle is calculated, and the tangent value is set as the static friction coefficient.

  By applying and infiltrating a chemical solution containing a predetermined amount of moisture into the sheet constituting the two-ply tissue paper, the crepe structure of the sheet is extended, and the tissue paper having a smooth surface is formed. Further, since the paper thickness is reduced and the fiber density is increased by the elongation, the strength between fibers is increased, and a tissue paper having a high tensile strength in the CD direction can be obtained. Whereas conventional moisturizing tissue applies a lotion solution to a thick base paper to create a film on the surface of the tissue to give the user smoothness, the present invention suppresses the thickness and the amount of solution applied, and provides a crepe structure. The surface is made smooth by stretching, thereby providing a smoothness higher than that of a conventional moisturizing tissue. In other words, the sticky feeling is reduced as a minimum amount of the lotion solution film on the tissue surface to make it feel smooth. Therefore, the drug content in the dry state is lower than that of conventional lotion type tissue paper, and it contains a sufficient amount of drug to exert its effect even though it does not easily cause stickiness when used. Therefore, it has enough moist and moisturizing properties. Furthermore, since the paper thickness is thin, it has a soft feeling in use as compared with the drug content.

  By using a multi-stand type interfolder, the manufacturing speed can be increased. When the multi-stand type interfolder is used, the manufactured tissue paper product has a form in which the consumer pulls out the tissue paper in the CD direction. However, the conventional moisturizing tissue does not have high paper strength, particularly the tensile strength in the CD direction, as compared to the non-humidifying tissue, so that a product manufactured by a multi-stand type interfolder is easily broken when pulled out. A problem is assumed.

  In the tissue paper product according to the present invention, as described above, the tissue paper has a strong tensile strength in the CD direction and a small coefficient of static friction, and is flexible as a tissue paper storage box on the film around the outlet. Is used, and the size of the outlet is specified. Thereby, even if the tissue paper is pulled in the CD direction and taken out, it is difficult to break, and the uppermost layer is difficult to fall into the box from the take-out port. When folding with a multi-stand type interfolder for moisture-retaining tissue paper, a continuous sheet containing moisture is processed while applying a relatively high tensile force in the MD direction and applying pressure in the thickness direction. The web bulk can be kept lower than when using a folder. By this effect, it can be stored in a compact storage box frequently used for non-humidifying tissue paper products.

  As described above, the present invention provides a tissue paper having a moist and smooth texture equal to or higher than that of a conventional moisturizing tissue, having less stickiness than the conventional moisturizing tissue, and having a high tensile strength in the CD direction. Is. In addition, since tissue paper can be pulled out from the storage box in the CD direction, a chemical-coated tissue paper product that can be manufactured at high speed using a multi-stand type interfolder is provided. Furthermore, the chemical | medical solution application | coating tissue paper products accommodated in the compact type | mold storage box are provided.

It is a figure which shows the apparatus outline | summary of the ply process of the tissue paper of 1st Embodiment which concerns on this invention. It is the schematic which shows an example of a multi stand type inter folder, and has shown the state seen from the front. It is the schematic which shows an example of a multi stand type inter folder, and has shown the state seen from the side. It is the schematic which shows an example of a multi stand type inter folder, and has shown the state seen from the front. It is a longitudinal cross-sectional view of the folded tissue paper. It is a principal part expansion perspective view of the site | part regarding a folding plate. It is a principal part expansion perspective view which shows how to fold a secondary continuous sheet (tissue paper). It is a principal part expansion perspective view which shows how to fold a secondary continuous sheet (tissue paper). It is a principal part expansion perspective view which shows how to fold a secondary continuous sheet (tissue paper). It is a figure which shows a mode that the (a) tissue paper bundle | flux of 1st Embodiment is accommodated in the storage box. (B) It is a partially broken figure which shows a mode that the tissue paper accommodated in the storage box is taken out. It is a figure which shows the measuring method of the MMD value of tissue paper. It is a perspective view which shows an example of the tissue paper product which concerns on this invention. It is an inner surface development view of the storage box of the tissue paper product of FIG. It is a perspective view which shows the other example of the tissue paper product which concerns on this invention. It is an inner surface expanded view of the storage box of the tissue paper product of FIG.

Hereinafter, embodiments of the present invention will be described in detail.
[Example of structure]
The base paper of the tissue paper according to the present invention has a ply structure in which two thin papers (hereinafter also referred to as sheets) are laminated.

[Thin paper]
On the other hand, as the raw pulp of the thin paper (sheet) constituting the tissue paper according to the present invention, for example, mechanical pulp such as ground wood pulp (GP), pressure-rise ground wood pulp (PGW), thermomechanical pulp (TMP), etc. : Chemical pulps such as semi-chemical pulp (SCP), softwood high yield unbleached kraft pulp (HNKP), softwood bleached kraft pulp (NBKP), hardwood unbleached kraft pulp (LUKP), hardwood bleached kraft pulp (LBKP), etc .: deink Examples include waste paper pulp such as depulp (DIP) and waste pulp (WP). The raw material pulp can be used by selecting one kind or two or more kinds. Preferably, a chemical pulp containing no filler or foreign matter is preferred. Further, the raw material pulp may contain woody materials such as straw pulp, bamboo pulp, kenaf pulp, and herbs.

  In particular, the raw material pulp is preferably a blend of NBKP and LBKP. Waste paper pulp may be blended as appropriate, but in terms of texture and the like, it is preferably composed only of NBKP and LBKP. In this case, the blending ratio is NBKP: LBKP = 20: 80 to 80:20. In particular, NBKP: LBKP = 30: 70 to 60:40 is desirable.

  On the other hand, in papermaking raw materials, other fiber raw materials include polyethylene terephthalate, polybutylene terephthalate, and polyester fibers such as copolymers thereof, polyolefin fibers such as polyethylene, polypropylene, and polystyrene, acrylics such as polyacrylonitrile and modacrylic. Fiber, polyamide fiber such as nylon 6, nylon 66, nylon 12, etc., synthetic fiber such as polyvinyl alcohol fiber, polyvinylidene chloride fiber, polyvinyl chloride fiber, urethane fiber, semi-synthetic fiber such as triacetate fiber, diacetate fiber, screw Include regenerated cellulose fiber such as coarse rayon, copper ammonia rayon, polynosic rayon, lyocell, and chemical fiber such as regenerated fiber spun from solution of collagen, alginic acid, chitin, etc. It is possible. The polymer constituting the chemical fiber may be in the form of a homopolymer, a modified polymer, a blend, a copolymer or the like.

  Raw materials such as pulp fibers are used as a base paper through, for example, a known papermaking process, specifically, a wire part, a press part, a dryer part, a calendar part, and the like. In this papermaking, for example, a dry paper strength enhancer, a wet paper strength enhancer, a softener, a release agent, a coating agent, a viscosity agent (knurl), a pH adjuster such as caustic soda, an antifoaming agent, a dye, etc. Chemicals can be added.

[US tsubo]
The rice paper weight per sheet of the tissue paper according to the present invention is preferably 10 to 25 g / m ² , more preferably 11 to 16 g / m ² . If the rice tsubo is less than 10 g / m ² , it is preferable from the viewpoint of improving softness, but it is difficult to ensure adequate strength that can withstand use. On the other hand, when the rice tsubo exceeds 25 g / m ² , the entire paper becomes hard, and a feeling of stickiness is generated, resulting in poor touch. In addition, the US tsubo is based on the US tsubo measurement method of JIS P 8124 (1998).

[Crepe rate]
The crepe rate of the primary raw sheet constituting the tissue paper of the present invention is 10 to 30%, more preferably 13 to 20%. Here, the crepe rate is expressed by the following equation.
Crepe rate: {(peripheral speed of the dryer during papermaking)-(peripheral speed of the reel)} / (peripheral speed of the dryer during papermaking) × 100.

[Medical solution]
Tissue paper of the present invention, the drug combined duplex 1.5~5.0g / m ^2, more preferably 3.0~5.0g / m ² containing. If the drug content is less than 1.5 g / m ² , the effect of the drug is not exhibited, and if it exceeds 5.0 g / m ² , the tissue paper has a sticky feeling, and the dry tensile strength decreases.

  About the chemical | medical solution to apply | coat, it is preferable that a viscosity shall be 1-700 mPa * s at 40 degreeC from a viewpoint of performing high-speed processing, especially 50-400 mPa * s. If it is less than 1 mPa · s, the chemical solution is likely to scatter on rolls such as anilox roll, printing plate roll, and gravure roll, and conversely if it is greater than 700 mPa · s, it is difficult to control the amount of application to each roll or continuous sheet. Ingredients include 70-90% polyol, 1-15% moisture, and 0.01-22% functional chemicals. The water content of the chemical solution to be applied was determined by the Karl Fischer method.

  Polyols include polyhydric alcohols such as glycerin, diglycerin, propylene glycol, 1,3-butylene glycol, polyethylene glycol, and derivatives thereof, and sugars such as sorbitol, glucose, xylitol, maltose, maltitol, mannitol, and trehalose.

  Functional agents include softeners, surfactants, inorganic and organic fine particle powders, oily components, and the like. Softeners and surfactants have the effect of imparting flexibility to the tissue and smoothing the surface, and anionic surfactants, cationic surfactants and zwitterionic surfactants are applied. Inorganic and organic fine particle powders have a smooth surface. The oil component has a function of improving lubricity, and higher alcohols such as liquid paraffin, cetanol, stearyl alcohol, and oleyl alcohol can be used.

  In addition, as a functional agent, one of a hydrophilic polymer gelling agent, collagen, hydrolyzed collagen, hydrolyzed keratin, hydrolyzed silk, hyaluronic acid or a salt thereof, ceramide, etc. A moisturizing agent such as any combination can be added.

  Deodorants such as flavors, emollients such as various natural extracts, vitamins, emulsifiers that stabilize compounding ingredients, antifoaming agents, antifungal agents, organic acids, etc. An agent can be appropriately blended. Furthermore, you may contain the antioxidant of vitamin C and vitamin E.

Of the above components, it is preferable to use a polyhydric alcohol such as glycerin or propylene glycol as a main component in order to stabilize the viscosity and coating amount of the chemical solution.
The temperature at the time of chemical solution application is preferably 30 ° C to 60 ° C, preferably 35 ° C to 55 ° C.

[Amount of application]
The coating amount was calculated from the difference between each sheet basis weight when the chemical solution after ply was not applied during operation and each sheet basis weight immediately after the corresponding application.
(Coating amount g / m ²⁾ = (basis weight g / m ² immediately after coating) - (the basis weight g / m ² in the case of not applying)
The coating amount of both surface layers or the total coating amount of both surfaces is the total coating amount per unit area of the plyed tissue paper sheet, and the coating amount of each sheet is added.

[Drug content]
The drug content refers to the content of the drug component in a dry state (absolutely dry) contained in the unit area of tissue paper in the standard state of JIS P 8111 (1998). Specifically, in the applied chemical solution The content of components other than moisture shall be indicated. The unit area of the tissue paper is an area of the plyed sheet viewed from a viewpoint perpendicular to the plane, and does not mean the total area of each plyed sheet and its front and back surfaces.

[Drug content]
The chemical content is defined as a tissue paper product having a predetermined mass conditioned under JIS P 8111 (1998) as a denominator (A) (g), and the water content in the chemical solution contained in the tissue paper product having a predetermined mass. The ratio of (B) divided by (A) is expressed as (%), with the removed mass (B) (g) as a molecule.
(Drug content%) = (B) ÷ (A) × 100 (%)

[Drug density]
The chemical solution density is the drug content per volume of two-ply tissue paper in the standard state of JIS P 8111 (1998).

[Paper thickness]
The paper thickness of the tissue paper according to the present invention is 100 to 140 μm, more preferably 120 to 140 μm in a 2-ply state. If the paper thickness is less than 100 μm, it is preferable from the viewpoint of improving the softness, but it is difficult to ensure adequate strength as tissue paper. On the other hand, when the thickness exceeds 140 μm, the texture of the tissue paper is deteriorated and a feeling of tingling is generated during use.

  As a method for measuring the paper thickness, the specimen is fully conditioned under the conditions of JIS P 8111 (1998), and then the dial thickness gauge (thickness measuring instrument) “PEACOCK G type” (manufactured by Ozaki Seisakusho) under the same conditions. It shall be measured in the state of 2 plies using. Specifically, confirm that there is no dust, dust, etc. between the plunger and the measuring table, lower the plunger on the measuring table, move the memory of the dial thickness gauge to adjust the zero point, and then Raise the plunger, place the sample on the test bench, slowly lower the plunger and read the gauge at that time. At this time, only the plunger is placed. The terminal of the plunger is made of metal so that a circular plane having a diameter of 10 mm is perpendicular to the plane of the paper, and the load at the time of measuring the paper thickness is about 70 gf. The paper thickness is an average value obtained by performing measurement 10 times.

[Tensile strength]
The tensile strength of the tissue paper according to the present invention is measured in a two-ply state.
The dry tensile strength is measured according to the tensile test method of JIS P 8113 (1998). Among them, it is cut into a width of 25 mm in the vertical direction and the horizontal direction under the standard conditions defined in JIS P 8111 (1998).

  The dry tensile strength of the tissue paper according to the present invention is 180 to 350 cN / 25 mm in the MD direction, more preferably 160 to 300 cN / 25 mm, 80 to 120 cN / 25 mm in the CD direction, and more preferably 80 to 110 cN / 25 mm. The ratio of the direction / CD direction is preferably 1.5 to 3.0.

  The wet tensile strength is determined according to JIS P 8135 (1998). The wet tensile strength of the tissue paper is 70 to 160 cN / 25 mm in the MD direction, more preferably 80 to 130 cN / 25 mm, and 33 to 50 cN / 25 mm, more preferably 35 to 45 cN / 25 mm in the CD direction.

[Softness]
The softness value of the tissue paper of the present invention is preferably 0.80 to 1.10 cN / 100 mm. The softness here is measured based on the handle ohm method according to the JIS L 1096 E method.
However, the test piece was 100 mm × 100 mm in size, and the clearance was 5 mm. The measurement was performed 5 times each in the longitudinal direction and the lateral direction with 1 ply, and the average value of all 10 times was represented by 2 digits of decimal point and expressed in units of cN / 100 mm.

  By setting the softness within the above range, it is possible to reduce the resistance value when taking out the tissue paper to make it difficult to break, and to balance the feeling of thickness and softness.

〔Moisture percentage〕
The moisture content of the product is desirably 10.0 to 13.0%. The moisture content is determined based on JIS P 8127.
Moisture content (%) = {(weight of paper before drying) − (weight of paper after drying)} / (weight of paper before drying) × 100

〔Growth rate〕
The elongation in the MD direction of the product is desirably 11.0 to 15.0%. The elongation rate here is measured using “Universal Tensile Compression Tester TG-200N” manufactured by Minebea Co., Ltd. The elongation is the “stretch at break” described in “3. Definition e)” of JIS P8113.

[Static friction coefficient]
On the other hand, the tissue paper of the present invention desirably has a coefficient of static friction between tissue papers of 0.50 to 0.65, more preferably 0.55 to 0.60. The static friction coefficient here is measured by the following method according to JIS P 8147 (1998).
The tissue paper peeled off in one ply is attached to the acrylic plate so that the outer surface of the tissue paper is on the outside. Wrap tissue paper around a 100 g weight with 2 plies and place it on the tissue on the acrylic plate. Tilt the acrylic plate and measure the angle at which the weight slides down. Angle measurement is carried out 10 times in total, 5 times for each of the tissue in the vertical and vertical directions (MD and MD directions), and in the horizontal and horizontal directions (CD and CD directions), and the average angle is calculated. The tangent value is defined as a coefficient of static friction.

  The following can be considered as a principle for reducing the static friction coefficient. In the present invention, two primary raw fabric continuous sheets are plyed, the crepe peak is smoothed by calendering, the sheet surface is smoothed by smoothing the crepe peak, and then the lotion chemical solution Is preferably applied by a transfer method. The applied secondary raw sheet is stored under a certain tension and seasoned until it is folded. During this time, the lotion chemical solution spreads over time so as to be uniform inside the paper layer in a planar and thickness direction. In the subsequent process, when folding by the multi-stand type interfolder is performed, the secondary continuous sheet is pulled out from the ply raw fabric, folded, and cut through a process of pressing with a pull conveyor while pulling. In this folding process, folding processing is started in a state in which it is coated and seasoned and moisture is absorbed in the paper layer. Due to seasoning and subsequent tension and pressure in the thickness direction, unevenness due to creping on the sheet surface is reduced, and friction between sheets is reduced.

[MMD]
MMD is an average deviation (unit: dimensionless) of the friction coefficient μ. MMD is one of the indices of smoothness. The smaller the numerical value, the smoother, and the larger the numerical value, the less smooth.
As a method for measuring the MMD value, as shown in FIG. 11A, a tension of 20 g / cm is applied to the contact surface of the friction element 112 in a predetermined direction (downward and rightward in FIG. 11A). While being brought into contact with the surface of the tissue paper 111, which is the measurement sample, at a contact pressure of 25 g, it is moved 2 cm at a speed of 0.1 cm / s in the same direction as the direction in which the tension is applied. At this time, the friction coefficient was measured using a friction tester KES-SE (manufactured by Kato Tech Co., Ltd.), and the average deviation of the friction coefficient μ at a friction distance of 2 cm (moving distance was 3 cm and excluding 5 mm before and after each). Was defined as the MMD value.
The friction element 112 has 20 piano wires P with a diameter of 0.5 mm adjacent to each other, and has a contact surface formed so that the length and width are both 10 mm. The contact surface is formed with a unit bulging portion whose tip is formed of 20 piano wires P (curvature radius 0.25 mm).
FIG. 11A schematically shows the friction element 112, and FIG. 11B shows an enlarged view of a portion surrounded by an alternate long and short dash line in FIG. 11A.

[Web bulk]
A plastic plate having a weight of 30 g and a size of 130 mm × 250 mm was placed on the tissue paper bundle, and the heights of the four corners were averaged to obtain the web bulk value.
The web volume of the tissue paper according to the present invention is 0.25 to 0.40 mm per set. In particular, it is preferably 0.28 to 0.36 mm per set and 55 to 65 mm for 180 sets. If the web bulk is too low, it becomes difficult for the user to put the finger deeply out of the take-out opening when taking out the uppermost tissue from the storage box, making it difficult to take out. Further, if the web bulk is too high, it cannot be stored in a compact storage box (having a box height of about 55 to 65 mm), and manufacturing costs and transportation costs are increased, or the web is compressed during storage and is compact. In order to store in the storage box, the top layer must be pulled out with a strong force when taking out, and there is a problem that the tissue paper is easily torn.

[Product density]
The tissue paper according to the present invention is folded by an interfolder or the like, and is cut into a product size at any stage before or after the folding process. For example, 180 sets are packed into a product. The paper density after 180 sets of folding is preferably 0.15 to 0.25 g / cm ³ , more preferably 0.17 to 0.23 g / m ³ . If it is lower than 0.15 g / cm ³ , moist feeling and smoothness cannot be obtained, and if it is higher than 0.25 g / cm ³ , the thickness of the tissue paper is impaired and a sticky feeling is produced, and the water absorption is deteriorated. End up.
The product density is the paper thickness (D) of tissue paper (2 ply) according to “PEACOCK G type”, which is a double value (C) of the tissue paper product tsubo conditioned under JIS P 8111 conditions. The unit is expressed in g / cm ³ and 3 decimal places.
((Density (g / cm ³ )) = (C (g / m ² )) × 2 ÷ (D (μm))

[Storage box]
12 shows a tissue paper product according to the present invention, and FIG. 13 shows a view of the storage box 201 as seen from the inside of the box in the unfolded state. As a material for forming the box, any known material used as a tissue paper storage box such as cardboard having a basis weight of 300 to 450 g / m ² can be used. The tissue paper storage box 201 has a rectangular parallelepiped shape in an assembled state as shown in FIG. 12, and includes a pair of upper and lower upper surfaces 202 and 203, a pair of front and rear front surfaces 204 and 205, and a pair of left and right left sides. A surface 204 and a right side 205. In this case, the front and rear surfaces 204 and 205 and the left and right side surfaces 206 and 207 correspond to the peripheral surface of the present invention.

  As can be seen from the developed state of FIG. 13, the adhesive margin piece 203b extends from the rear edge of the lower surface (the edge adjacent to the rear surface of the peripheral edge) over the entire long side, and the adhesive margin piece 203b overlaps the inner side of the rear surface. Then, a cylindrical portion composed of the upper surface 202, the lower surface 203, the front surface 204, and the rear surface 205 is formed by being bonded and fixed by an adhesive such as a hot melt adhesive.

  The left and right side surfaces 204 and 205 extend from an adjacent edge of the upper surface 202 and an adjacent edge of the lower surface 203, respectively, and from an adjacent edge of the front surface 204 and an adjacent edge of the rear surface 205, respectively. The front flap 204f and the rear flap 205f, the upper flap 202f and the lower flap 203f are overlapped on the outside of the front flap 204f and the rear flap 205f, and the upper flap 202f and the lower flap 203f are the front flap and the rear flap 205f. The lower end portion of the upper flap 202f is overlapped on the outer side of the upper end portion of the lower flap 203f, and the overlapped portion is fixed by the adhesive.

  The inner dimension of the box is preferably 5 to 20 mm, particularly 8 to 15 mm longer than the length in the longitudinal direction of the web to be stored. By providing a gap in the longitudinal direction inside the storage box, it becomes possible to take out the tissue paper with almost no resistance between the inner surface of the box and the tissue paper.

  The height of the storage box can be arbitrarily determined within the scope of the present invention in accordance with the number of web sets to be stored. The height of the storage box is preferably 50 to 120 mm.

  Furthermore, the height of the storage box is preferably 50 to 80 mm, more preferably 55 to 65 mm, in order to reduce manufacturing costs and transportation costs.

  A cutout such as a perforation is formed in advance on the upper surface 202 of the storage box 201, and an extraction window (opening) 202a is formed by peeling off the lid portion 202b surrounded by the cutout at the start of use. It has become. As shown in FIGS. 14 and 15, the lid portion 202 b may be configured so as to be a valley fold line 202 g without being cut off at substantially one side. By setting it as such a structure, the cover part 2b can be utilized as a cover of the extraction window 202a. Alternatively, the take-out window 202a may be opened in advance and the lid portion 202b may not be provided. The length in the long side direction of the take-out window 202a is 50 to 70%, particularly 55 to 65% of the length in the longitudinal direction of the web to be stored. The length in the short side direction of the take-out window 202a is preferably 35 to 55%, particularly 40 to 50% of the length in the short side direction of the web.

  A film-like cover sheet 202c is attached to the take-out window 202a from the inside of the box with a hot-melt adhesive or the like, and a portion of the cover sheet 202c surrounded by the take-out window 202a has a long side direction of the box 1 A slit 202s is formed. The slit 202s is 45 to 65%, particularly 50 to 60% of the length in the longitudinal direction of the web to be stored. The slit 202s is particularly preferably arranged in the vicinity of the center of the extraction window 202a in both the long side direction and the short side direction.

  As a material for forming the cover sheet, a resin film sheet made of a resin such as polyethylene, polypropylene, polyester, or a laminated resin film sheet obtained by laminating these, a laminated film sheet laminated with a film sheet and a thin paper, etc. Examples include synthetic paper sheets made of fibers. A resin film sheet is preferable in consideration of the take-out property, and a low-density polyethylene film (LDPE) that is particularly flexible and low in production cost can be suitably used.

  The thickness of the film is desirably 33 to 38 μm. Further, it is preferable that the longitudinal bending resistance of the film is 0.8 to 1.4 gf / 10 mm, particularly 1.0 to 1.2 gf / 10 mm. The bending resistance was measured based on the handle ohmmeter method described in JIS L 1096 E method. The test piece was 100 mm long × 10 mm wide, and the clearance was 5 mm. The average value of 10 times in 1 ply in the vertical direction was represented by 2 digits of decimal point and expressed in units of cN / 100 mm. The longitudinal direction of the film coincides with the slit direction of the film. If the bending resistance of the film in the longitudinal direction is higher than 1.4 gf / 10 mm, it will be easy to tear when taking out the tissue paper, and if it is lower than 0.8 gf / 10 mm, it will be difficult to hold the tissue paper in the outlet and pop-up will occur. It becomes difficult.

  Furthermore, the coefficient of static friction between the lateral direction of the film and the tissue paper (the removal direction) is 0.20 to 0.30, more preferably 0.23 to 0, in order to improve the slip of the tissue paper at the time of taking out and suppress the resistance. .28. The film transverse direction means a direction perpendicular to the film longitudinal direction and the film plane. The coefficient of static friction between the film and tissue paper was measured by the following method. The film is affixed to the acrylic plate so that the slope direction is the lateral direction of the film so that the inner surface of the storage box is on the outside. Wrap tissue paper around a 100 g weight with 2 plies, and place it on the film on the acrylic plate so that the slope direction is the tissue removal direction. Tilt the acrylic plate and measure the angle at which the weight slides down. The angle measurement was performed 10 times, the average angle was calculated, and the tangent value was taken as the static friction coefficient.

[Tissue paper removal resistance]
By setting the resistance applied when taking out the tissue paper within a certain range, it is possible to minimize tearing during the taking out. The tissue paper take-out resistance is measured by the following method. Secure the center tip of tissue paper to the gauge tip of the pushbull gauge, and take the tissue paper vertically from the storage box with the bottom surface fixed at a constant speed over a period of 0.4 to 0.6 seconds. The resistance value was measured. The tissue paper to be taken out is a total of 5 sets from the first set to the 5th set from the top layer, and a total of 5 sets from the 11th set to the 15th set. It was. The take-out resistance is preferably 70 gf or less, more preferably 50 to 70 gf.

[Example of manufacturing method]
The tissue paper of the present invention described above can be manufactured as follows. In FIG. 1, the outline | summary of the apparatus of the ply process of the tissue paper which concerns on this invention was shown. In addition, it is preferable to implement the process which concerns on FIG. 1 with the ply machine which is an apparatus integrated with the coating device (on-machine coating).

  The base paper produced by the paper machine is creped as a continuous sheet, calendered, and wound up to form primary rolls 11 and 12 (generally also called jumbo rolls). The

  The continuous sheets 31 and 32 are laminated by the laminating roller 13 to form two plies, and if necessary, calendered by the ply machine calendar 14 and sent to the chemical solution coating process. Any known coating method such as dipping, spraying, flexo coating, and gravure coating can be used as the chemical coating method, but printing methods such as gravure coating and flexographic coating that perform chemical coating evenly on the entire coated surface In particular, it is more preferable to use a flexo coater equipped with a doctor chamber 15 because a chemical solution can be supplied in a stable coating amount.

  In the ply process of FIG. 1, two flexo coaters 16 and 17 are provided, and a chemical solution is applied to each surface of a two-ply continuous sheet.

  When the flexographic printing method is used as the chemical solution applying means, the processing speed is 100 to 1100 m / min, preferably 350 to 1050 m / min, particularly preferably 450 to 1000 m / min. If it is less than 100 m / min, the productivity is low, and if it is more than 1100 m / min, uneven coating occurs and the chemical solution is likely to scatter. The number of lines of the flexographic printing plate roll is 10 to 60 lines, preferably 15 to 40 lines, and particularly preferably 20 to 35 lines. If the number of lines is less than 10, many coating irregularities occur. On the other hand, if the number of lines exceeds 60 lines, the paper dust tends to clog. The number of lines of anilox roll is 10 to 300 lines, preferably 25 to 200 lines, particularly preferably 50 to 100 lines. If the number of lines is less than 10, many coating irregularities occur. On the other hand, if the number of lines exceeds 300 lines, the paper dust tends to be clogged. The anilox roll has a cell capacity of 10 to 100 cc, preferably 15 to 70 cc, particularly preferably 30 to 60 cc. If the cell capacity is less than 10 cc, a desired coating amount cannot be obtained. On the other hand, if the cell capacity is more than 100 cc, the amount of chemical solution scattered increases. By setting it as such a structure, a chemical | medical solution is transcribe | transferred to the crepe peak part of a continuous sheet in the shape of a dot of 1 mm or less, and a uniform application | coating sheet is obtained.

The flexographic printing method can stabilize the coating amount even when the processing speed is high, and can stably apply a wide range of chemical viscosity with a single roll.
When the gravure printing method is used as the chemical solution applying means, the processing speed is 100 to 1000 m / min, preferably 350 to 950 m / min, particularly preferably 450 to 950 m / min. When it is less than 100 m / min, productivity is low, and when it is more than 1000 m / min, coating unevenness occurs and the chemical solution is likely to be scattered. The number of gravure rolls is 40 to 160 lines, preferably 60 to 140 lines, particularly preferably 80 to 120 lines. If the number of lines is less than 40 lines, the amount of chemical solution scattered increases, whereas if the number of lines exceeds 160 lines, paper dust tends to be clogged.

  When the chemical spraying method is used as the chemical coating means, the spraying means is not particularly limited, but may be a nozzle dampening method or a rotor dampening spraying method. The processing speed is 100 to 1100 m / min, preferably 350 to 1050 m / min, and more preferably 450 to 1000 m / min.

  The sheet after application of the chemical solution is supplied to a contact embossing roller 18 and a roller roll 19 and fixed by subjecting a two-ply continuous sheet to a contact embossing (knurling) process. At this time, the continuous sheet 32 with a small amount of chemical solution applied is disposed so as to contact the contact embossing roller 18. The contact embossing is preferably applied uniformly in the vertical direction with a width of 1 to 10 mm at positions of 1/10 to 1/20 with respect to the paper width from both sides. Any of the known methods such as fixing the ply with an adhesive may be used. However, when using an adhesive, there is a problem that the touch tends to become hard, and it is easy to peel off when applying a chemical solution. It can be said that the use of embossing is more preferable.

2 ply continuous sheet with contact embossing is cut directly into product size after being subjected to folding processing by being directly applied to a rotary interfolder or the like, or after being cut into product width by slitter 20, The winding roll 21 makes a take-up secondary raw roll 22 which is folded and stored in a paper box.
In this embodiment, the chemical solution is applied before the contact embossing. However, the chemical solution may be applied after the contact embossing.

  Chemical solution application may be performed either on-machine or off-machine. Further, the chemical solution applying means may be provided before the winding process of the primary continuous sheet of the paper machine (if the calendar process is performed, it may be before or after the calendar process) or before the interfolder is folded. Furthermore, the chemical solution application means is not limited to a single one, and may be configured to apply the chemical solution in a plurality of steps.

[Multi-stand type inter folder]
The secondary raw roll described above is subjected to a folding process particularly in tissue paper products. As the folding process, a known method such as a rotary interfolder or a multi-stand interfolder can be used, but it is more preferable to use a multi-stand interfolder with high productivity. In the present invention, as described above, it is necessary to use a multi-stand type interfolder because the static friction coefficient of tissue paper needs to be low and the web bulk needs to be low.

  A large number of secondary web rolls 22 are set in a multi-stand type interfolder, and a tissue paper bundle is manufactured by drawing out a secondary continuous sheet from the set secondary web roll 22 and folding and stacking them. Hereinafter, an example of the multi-stand type interfolder will be described.

  2 and 3 show an example of a multi-stand type interfolder. Reference numeral 2 in the drawing denotes secondary raw rolls 22, 22... Set on secondary raw roll support portions (not shown) of the multi-stand type interfolder 1. These secondary raw rolls 22, 22... Are set side by side in the direction (the horizontal direction in FIG. 2, the front-to-back direction in FIG. 3) in which the required number is orthogonal to the illustrated plane. Each secondary raw roll R has slits in the width of tissue paper product in the above-described manufacturing equipment and manufacturing method of the secondary raw roll for tissue paper products. It is wound and set in double width.

  The continuous belt-like secondary continuous sheets 63A and 63B unwound from the secondary raw roll 22 are guided by guide means such as guide rollers G1 and G1 and fed into the folding mechanism section 60. Moreover, the folding mechanism part 60 is provided with the folding plate group 64 in which the required number of folding plates P, P ... are arranged in parallel as shown in FIG. For each folded plate P, guide rollers G2, G2 and guide round bar members G3, G3 for guiding a pair of continuous secondary continuous sheets 63A or 63B are respectively provided at appropriate positions. Further, below the folded plates P, P..., A conveyor 65 is provided that receives and conveys the laminated band 67 that is stacked while being folded.

  A folding mechanism using this type of folded plates P, P... Is a known mechanism, for example, from US Pat. As shown in FIG. 5, this type of folding mechanism folds each continuous secondary continuous sheet 63A, 63B... In the Z-shape and is adjacent to the adjacent secondary continuous sheets 63A, 63B. Stack the ends together.

  FIGS. 6 to 9 show in detail the portions of the folding mechanism 60 that are particularly related to the folded plate P. FIG. In the folding mechanism 60, a pair of continuous secondary continuous sheets 63A and 63B are guided for each folded plate P. At this time, the continuous secondary continuous sheets 63A and 63B are guided by the guide round bar members G3 and G3 while being shifted in position so that the side end portions do not overlap each other.

  The continuous secondary continuous sheet that overlaps the lower side when guided by the folded plate P is the first continuous secondary continuous sheet 63A, and the continuous secondary continuous sheet that overlaps the upper side is the second continuous sheet. As shown in FIGS. 5 and 7, these continuous secondary sheets 63A and 63B are second continuous secondary continuous sheets of the first continuous secondary continuous sheet 63A. The side end e1 that does not overlap the sheet 63B is folded back to the upper side of the second continuous secondary continuous sheet 63B by the side plate P1 of the folded plate P, and as shown in FIG. 5 and FIG. The side end portion e2 of the continuous secondary continuous sheet 63B that does not overlap the first continuous secondary continuous sheet 63A is folded downward so as to be drawn under the folded plate P from the slit P2 of the folded plate P. . At this time, as shown in FIGS. 5 and 9, the side end e3 (e1) of the continuous secondary continuous sheet 63A stacked while being folded in the upstream folded plate P is second from the slit P2 of the folded plate P. Are guided between the folded portions of the secondary continuous sheet 63B. In this way, each continuous secondary continuous sheet 63A, 63B... Is folded in a Z shape and the side ends of adjacent continuous secondary continuous sheets 63A and 63B are crossed together, so that the product is used. In some cases, when the top tissue paper is pulled out, the side edge of the next tissue paper is pulled out.

  As shown in FIG. 2, the laminated band 70 obtained in the multi-stand type interfolder 6 as described above is cut (cut) at a predetermined interval in the flow direction FL by the cutting means 66 at the subsequent stage, and the tissue is cut. This tissue paper bundle 30a is further stored in the storage box B in the subsequent equipment as shown in FIG. 10 (a). In the multi-stand type interfolder 1 as described above, the paper direction of the laminated band 70 is the vertical direction (MD direction) along the flow direction FL, and the horizontal direction along the direction orthogonal to the flow direction. Direction (CD direction). For this reason, the direction of the paper of the tissue paper constituting the tissue paper bundle 67a obtained by cutting the laminated band 70 into a predetermined length is along the folding direction of the tissue paper as shown in FIG. The horizontal direction (CD direction) and the vertical direction (MD direction) along the direction orthogonal to the folding direction of the tissue paper.

  FIG. 10B shows an example of a product in which the tissue paper bundle 67a is stored in the storage box B. A perforation M is provided on the upper surface of the storage box B, and a part of the upper surface of the storage box B is broken by the perforation M so that the upper surface of the storage box B is opened. The opening is covered with a film F having a slit at the center, and the tissue paper T can be taken out through the slit provided in the film F.

  By the way, as described above, the direction of the paper of the tissue paper constituting the tissue paper bundle 67a is the horizontal direction (CD direction) along the folding direction of the tissue paper, as shown in FIG. When the tissue paper T is pulled out from the storage box B, the pulling direction is along the horizontal direction (CD direction) of the tissue paper T.

In order to confirm the effect of the present invention, Table 1 shows the results of evaluating the dimensions of the product and the paper quality of the tissue paper for the examples and comparative examples according to the present invention.
Examples 1 to 7 are tissue papers according to the present invention manufactured using a multi-stand type interfolder for folding.

  Comparative Examples 1 to 4 are commercially available products, Comparative Example 1 is a non-moisturizing general purpose tissue paper, and Comparative Examples 2 to 4 are moisturizing lotion type tissue papers.

  The composition of the chemical solution applied to Examples 1 to 7 was adjusted as shown in Table 2. The method for measuring tissue weight, paper thickness, tensile strength, elongation, softness, coefficient of static friction, moisture content, MMD, and tissue resistance of tissue paper is described in the section of the embodiment for carrying out the invention. Just as you did. The drug content indicates the ratio of the dry weight of the drug to the tissue paper basis weight.

  Table 1 shows the inner dimensions of the storage boxes for the tissue paper products of Examples 1 to 7 and Comparative Examples 1 to 4, the dimensions of the take-out window, the length of the slit, the material, thickness, and Clark stiffness of the film.

Along with the evaluation of paper quality, sensory evaluation based on the following criteria was performed for 10 people in Examples 1 to 7 and Comparative Examples 1 to 4 for softness, smoothness, thickness, and moist feeling. The sensory evaluation was performed on the basis of the following criteria, with all results of Comparative Example 1 being a non-humidifying tissue paper set to 3.
5: Very good 4: Excellent 3: Equivalent to the standard 2: Inferior 1: Notably inferior The tissue-coated tissue paper was also evaluated for the presence or absence of stickiness.
○: Little sticky feeling ×: Clearly sticky feeling
The ease of taking out the tissue paper was evaluated as follows by carrying out the taking out operation for 10 people.
○: Resistance at the time of taking out was small, and there was no tear.
Δ: 1 to 4 people broke or complained of difficulty in taking out due to resistance.
X: Five to ten people complained of tearing.
Regarding the presence or absence of the tissue paper in the storage box, for 10 people, all tissue paper products were taken out from the first set to determine whether or not there was any depression.
○: There was no depression.
Δ: 1 to 4 people experienced a drop once or more.
X: 5-10 people experienced the depression once or more.
The difficulty of tearing at the time of use was evaluated by using tissue paper as a nose for 10 persons and determining whether there was any tear.
○: 3 or fewer people were torn or not torn.
Δ: 4 to 8 people were torn.
X: 9 to 10 persons were torn.

The tissue paper according to the present invention showed high values of the dry tensile strength and the wet tensile strength in the CD direction as compared with a commercially available moisturizing tissue. The wet tensile strength in the CD direction was higher than that of conventional general-purpose tissue paper. It was also shown that the softness and static friction coefficient were lower than those of commercial products, and the paper was smooth and soft.
In sensory evaluation, the tissue paper according to the present invention is not excellent in thickness, but has a softness, smoothness, moist feeling equal to or higher than that of a moisturizing tissue, and a sticky feeling seen in a moisturizing tissue. I found out that it was alleviated.

  In particular, the following factors can be considered as factors that have good slipperiness for the tissue paper according to the present invention. Although it depends on the permeability of the chemical applied to tissue paper, when a chemical containing both hydrophilic and lipophilic components is applied, the hydrophilic components are absorbed into the pulp and the lipophilic components tend to remain on the paper surface. It is considered that surface friction is reduced. However, increasing the amount of chemical solution applied as in conventional moisturizing tissue, the hydrophilic component is not sufficiently absorbed into the pulp and remains on the surface, reducing the friction-reducing effect of the lipophilic component and hydrophilic components (such as glycerin). It is presumed that the slipperiness decreases due to the viscosity of.

In Examples 1 to 7, significantly better results than Comparative Examples 1 to 3 were obtained regarding the resistance to taking out tissue paper and the ease of taking out tissue paper. Thereby, it can be said that the risk of tearing at the time of taking out was reduced because slipping when taking out the tissue paper was good and the tissue paper could be taken out smoothly. In Comparative Example 4, there is a gap between the web and the inner surface of the upper portion of the box, and the web is softly inserted. Therefore, friction between the sheets hardly occurs, and the take-out resistance is small. However, the comparative example 4 has a problem that the sheet is likely to drop during use and is difficult to pop up. Compared with this, even if Example 1-4 improves sliding, it turns out that the tissue paper in use does not fall into the inside of a storage box from a slit part, and does not impair a usability even in the middle of use. It was.
Moreover, in Comparative Examples 2-4, it turned out that the tear at the time of use tends to arise, but Examples 1-7 are hard to produce a tear.

  As described above, the tissue paper according to the present invention has a sticky feeling seen in conventional moisturizing tissue and has a softness, smoothness, and moist feeling equivalent to or higher than that of the moisturizing tissue. It turned out to be. Further, it was found that the tissue paper can be taken out smoothly and is not easily torn at the time of taking out.

  The tissue paper and tissue paper product of the present invention can be used for tissue paper and tissue paper products used for wiping applications, in particular, body wiping applications, and facial applications.

Claims (4)

A tissue paper product in which a two-ply tissue paper coated with a chemical on its surface is folded in a pop-up manner and stored in a substantially rectangular storage box,
The tissue paper has a drug content of 1.5 to 5.0 g / m ^{2 on} both sides,
The basis weight per layer of the sheet constituting 2 plies is 10 to 25 g / m ² ,
2-ply paper thickness is 100-140 μm,
The storage box is made of a paper box having an opening on the upper surface in parallel with the long side direction, the opening being covered with a film attached to the inner surface of the storage box, and the film is a slit parallel to the opening in the long side direction. Have
A tissue paper product in which the film has a thickness of 33 to 38 μm and a longitudinal bending resistance of 0.8 to 1.4 gf / 10 mm.   The tissue paper product of Claim 1 whose moisture content of the said chemical | medical solution is 1 to 15%.   The tissue paper product according to claim 1, wherein the dry tensile strength in the CD direction of the two plies of the tissue paper is 80 to 120 cN / 25 mm.   The tissue paper product according to claim 1, wherein a coefficient of static friction between sheets of the tissue paper is 0.50 to 0.65.

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