JP5985804B2 - Moisturizing tissue paper product and method for producing moisturizing tissue paper - Google Patents

Description

  The present invention relates to a moisturizing tissue paper product and a method for producing a moisturizing tissue paper.

  Tissue paper is roughly classified into non-moisturizing tissue and moisturizing tissue. The moisturizing tissue is obtained by applying a moisturizing agent such as glycerin to the tissue base paper that has been made, and the non-humidifying tissue is one in which the moisturizing agent is not applied to the tissue base paper.

  The tissue paper is mainly used for wiping various objects. However, in the market, the above non-moisturizing tissue is a general-purpose product that does not limit the wiping target. It is marketed as a product specialized for use, and both are recognized by consumers as having different product categories.

  And as for the products related to the conventional moisturizing tissue as described above, as a product specification, the moisturizing agent is applied to the thick base paper especially in comparison with the general-purpose type non-humidifying tissue. However, the paper thickness compensates for the paper strength reduction caused by the moisturizing agent and the paper strength reduction when the runny nose is absorbed.

  However, since the conventional moisturizing tissue contains a relatively large amount of moisturizing agent, the moisturizing agent remains on the skin after biting the nose, and a sticky feeling may be felt. In addition, conventional moisturizing tissue was preferred by heavy users who blow their nose more than several times a day, mainly for allergic rhinitis and hay fever, but the softness, smoothness, Due to its moist feeling, the demand for general users has also increased, and it has been increasingly used for makeup and facial care other than nasal congestion.

  Against this backdrop, in recent years it is assumed that a wide range of facial care is used as well as nasal bleeds, and it is relatively thin but contains a moisturizer, improving the base paper, manufacturing method, moisturizer, etc., moisturizing A moisturizing tissue called general-purpose moisturizing tissue or general-purpose facial tissue that has a feeling, softness, and smoothness but has little stickiness and excellent versatility is commercially available and is forming a new product category.

  However, this type of general-purpose moisturizing tissue has revealed the following problems. First of all, even in general users, it may become a usage mode that is temporarily different from that of a heavy user, such as when suffering from a cold, and in such usage mode, a runny nose may easily penetrate and break when strongly biting the nose. there were. In addition, when used for facial care, a cosmetic that has been dipped in a cleansing solution and adhered to the skin or wrinkles may be rubbed off, and the surface strength may be weakly broken in such usage.

  In particular, tissue paper is generally made by packing 140 to 240 pairs in a storage box, but the conventional moisturizing tissue specialized for biting the nose is several tens of days a day such as allergic rhinitis and hay fever patients. Heavy users who blow their nose more than once were the main users, so they often used up tissue paper in a relatively short period of time, but in general-purpose moisturizing tissue, one product was used up compared to conventional moisturizing tissue. This period is long, and during that period, the paper strength drop due to the moisture absorption effect of the moisturizing agent becomes remarkable, which promotes the above-mentioned problems.

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

  Therefore, the main problem of the present invention is that it has a softness, smoothness and moist feeling equal to or higher than those of conventional moisturizing tissue paper, reduces stickiness during use, and easily breaks due to a decrease in paper strength. The object of the present invention is to provide a moisturizing tissue paper that improves the thickness and is excellent in versatility.

The present invention that has solved the above problems is as follows.
[Invention of Claim 1]
A moisturizing tissue paper product in which a two-ply moisturizing tissue paper containing a chemical containing a moisturizing agent is folded in a pop-up manner and stored in a substantially rectangular parallelepiped storage box,
In the moisturizing tissue paper product, the storage box is formed of a paper box having an opening on the upper surface parallel to the long side direction, and the opening is covered with a film attached to the inner surface of the storage box, and the film is long in the opening. It has a slit parallel to the side direction, the pulling direction when pulling out the moisturizing tissue paper from the storage box is a lateral direction, and
The moisturizing tissue paper
The tissue base paper contains 7.0-22.0 kg / t of wet paper strength agent and 1.0-8.0 kg / t of sizing agent,
The chemical solution contains a polyol and a functional drug containing an oil component,
The drug content of the drug solution is 2.0 to 6.0 g / m ² ,
The moisture content is 9.0-13.0%,
The basis weight per layer of the sheet constituting the two plies is 12 to 25 g / m ² ,
2-ply paper thickness is 100-160 μm,
The softness is 1.1 to 1.8 cN / 100 mm,
The dry tensile strength (lateral) is 80 to 140 cN / 25 mm,
Wet tensile strength (lateral) is 50 to 70 cN / 25 mm,
The ratio of dry tensile strength (longitudinal) / dry tensile strength (lateral) is 3.4 to 4.0 ,
The static friction coefficient measured by the following procedures (A) to (D) is 0.53 to 0.68.
Moisturizing tissue paper product characterized by that.
(A) The moisturizing 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 moisturizing tissue paper at the time of two plies becomes the outside.
(B) A moisturizing tissue paper different from the moisturizing tissue paper is wound around a 100 g weight with 2 plies and placed on the moisturizing 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 MD direction of the moisturizing tissue paper and in the CD direction of the moisturizing tissue paper, and the average angle is calculated by measuring 8 times in total, 4 times each. Is the coefficient of static friction.

[Invention of Claim 2]
It is a manufacturing method of the moisture retention tissue paper of Claim 1,
A tissue produced by adding 7.0 to 22.0 kg / t of a wet paper strength agent and 1.0 to 8.0 kg / t of a sizing agent in an absolutely dry amount of active ingredients in a papermaking raw material, and making a paper with a crepe rate of 10 to 30%. After laminating two layers of base paper, a chemical solution containing 70 to 90% by weight of polyol, 1.0 to 15% by weight of water, and 0.01 to 15% by weight of a functional drug containing an oily component is 2.2 to 2% on both sides. 6.6 g / m ^{2 is} applied,
The manufacturing method of the moisture retention tissue paper characterized by the above-mentioned.

  In the present invention, a chemical solution containing a predetermined amount of moisture is applied to and penetrates into a sheet constituting a two-ply tissue paper, whereby the crepe structure of the sheet is extended and a tissue paper having a smooth surface is formed. In addition, the paper thickness is reduced by stretching, and the flexibility and softness are excellent.

  Here, while the conventional moisturizing tissue applies a lotion chemical to a thick base paper to create a film on the tissue surface and give the user smoothness, the present invention suppresses the thickness and the chemical application amount, The crepe structure is elongated to make the surface smooth, and this gives 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. That is, the drug content in the dry state is lower than that of conventional lotion type tissue paper, and it contains a sufficient amount of chemical solution 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 .

  At the same time, in the present invention, as a tissue base paper, it is made by adding 7.0-22.0 kg / t of a wet paper strength agent and 1.0-8.0 kg / t of a sizing agent in a papermaking raw material. Things are used. By making the tissue base paper containing the above-mentioned amount of wet paper strength agent, it becomes torn when it is bitten by the nose, and even if a wiping operation is carried out with a cleansing solution contained during facial care. Furthermore, by including the above amount of sizing agent, the moisture permeation rate decreases, and the moisture that touches one side of the tissue paper penetrates in the thickness direction of the paper and easily spreads in the direction of the paper surface. It becomes an aspect absorbed in a wide range. Furthermore, the spread of moisture on the paper surface prevents moisture from being excessively located on a part of the paper surface, thereby preventing tearing even by such an action.

Further, by including a sizing agent and a wet paper strength agent in the tissue base paper itself, a sufficient paper strength is ensured even if moisture is absorbed over time by the moisturizing agent.
Here, the contents of the sizing agent and the wet paper strength agent in the present invention are defined in combination with these synergistic effects and other configurations specific to the present application. That is, first, the inclusion of a sizing agent and a wet paper strength agent generally tends to harden the paper, so this effect is offset in the moisturizing tissue that requires smoothness, softness, and flexibility according to the present invention. Must not be such an amount. Further, in the present invention, since the crepe is stretched to express smoothness by applying a chemical solution containing predetermined moisture to the tissue base paper, the amount of the crepe cannot be sufficiently exhibited. From these viewpoints, in the present invention, the upper limit values of the sizing agent and the wet paper strength agent are set to 22 kg / t and 8.0 kg / t, respectively.

  In addition, by applying a chemical solution containing a predetermined amount of moisture to the tissue base paper using such sizing agent and wet paper strength agent, the fiber density is increased due to the extension of the crepe, and the interfiber strength is increased. The tensile strength in the direction (lateral), particularly wet tensile strength, is further increased, and the moisture-retaining tissue paper is excellent in versatility.

  As described above, according to the present invention, the texture has a soft and smooth texture equal to or more than that of the conventional moisturizing tissue, has no stickiness than the conventional moisturizing tissue, has sufficient paper strength, and is temporarily excessive. The present invention provides a moisturizing tissue paper that can be suitably used without being broken even in use modes involving excessive water absorption, such as nasal paper use, facial care use, and liquid wiping, and is excellent in versatility.

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 figure which shows the apparatus outline | summary of the ply process of the tissue paper of 2nd Embodiment which concerns on this invention. It is the schematic which shows an example of the chemical | medical solution application | coating process of an off machine.

Hereinafter, embodiments of the present invention will be described in detail.
"Moisturizing tissue paper"
[Example of structure]
The moisturizing tissue paper according to the present invention (hereinafter also simply referred to as moisturizing tissue) has a two-ply structure in which two crepe papers are laminated. With 1 ply or 3 plies or more, it is difficult to sufficiently exhibit the desired effect of the present invention in relation to other configurations of the present invention.

[Tissue base paper]
On the other hand, the tissue base paper according to the moisturizing tissue of the present invention is a crepe paper, which is a papermaking material made from pulp as a main raw material.
The pulp is preferably a blend of NBKP (conifer kraft pulp) and LBKP (hardwood kraft pulp). Waste paper pulp or the like may be blended as appropriate, but in terms of texture and the like, it is particularly preferable that the pulp is composed only of NBKP and LBKP virgin pulp. In this case, the blending ratio is preferably NBKP: LBKP = 20: 80 to 80:20, and particularly preferably NBKP: LBKP = 30: 70 to 60:40.

  As other raw material pulp, for example, mechanical pulp such as ground wood pulp (GP), pressure-rise ground wood pulp (PGW), and thermomechanical pulp (TMP): semi-chemical pulp (CP), high yield of softwood Chemical pulps such as bleached kraft pulp (HNKP), softwood bleached kraft pulp (NBKP), hardwood unbleached kraft pulp (HNKP), hardwood unbleached kraft pulp (LUKP), etc .: deinked pulp (DIP), waste pulp (WP) And used paper pulp. 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 addition, in the papermaking raw materials, as fiber raw materials other than pulp, polyester fibers such as polyethylene terephthalate, polybutylene terephthalate, and copolymers thereof, polyolefin fibers such as polyethylene, polypropylene, and polystyrene, acrylic resins such as polyacrylonitrile, modacrylic, etc. 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 Includes chemical fibers such as regenerated fiber spun from regenerated cellulose fiber such as coarse rayon, copper ammonia rayon, polynosic rayon, lyocell, collagen, alginic acid, chitin, etc. Rukoto can. The polymer constituting the chemical fiber may be in the form of a homopolymer, a modified polymer, a blend, a copolymer or the like.

  On the other hand, the moisture-retaining tissue according to the present invention is characterized in that the tissue base paper has a wet paper strength agent of 7.0 to 22.0 kg / t, preferably 12.0 to 20.0 kg / t in size. It is made by adding 1.0 to 8.0 kg / t of an agent, preferably 1.2 to 6.0 kg / t. In addition, kg / t represents the ratio of wet paper strength agent and sizing agent active ingredient absolute dry amount per ton of dry pulp in kg.

  Specific examples of the wet paper strength agent include urea formaldehyde resin, melamine formaldehyde resin, polyamide polyamine epichlorohydrin, and the like. Of these, polyamide polyamine epichlorohydrin is preferably used. As the sizing agent, a neutral sizing agent that can be fixed in a neutral region is optimal. Specific examples include AKD (alkyl ketene dimer), styrene acrylic polymer, rosin sizing agent, and higher fatty acid amide sizing agent. Alkyl ketene dimers are particularly suitable. When a small amount of sulfuric acid band (aluminum sulfate) is added together, the fixing property is improved.

On the other hand, the tissue base paper according to the present invention forms a papermaking raw material through a known papermaking process, specifically, a wire part, a press part, a dryer part, and the like.
Here, the crepe rate of the tissue base paper according to the moisturizing tissue of the present invention is 10 to 30%, more preferably 13 to 22%. In the present invention, when the crepe rate is within this range, smoothness due to the extension of the crepe due to the application of the chemical solution is effectively expressed. 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.

[Drug]
Moisturizing tissue of the present invention, the drug 2.0 to 6.0 g / m ^2, preferably 3.0~5.0g / m ² containing. If the drug content is less than 2.0 g / m ² , the effect of the chemical solution will not be exhibited, and if it exceeds 6.0 g / m ² , a sticky feeling will be produced, and particularly suitable wet paper strength will be ensured. It becomes difficult. Here, the drug refers to an active ingredient in a chemical solution, and specifically refers to a portion excluding moisture in the chemical solution.

  The composition of the chemical solution contains at least 70 to 90% by weight of polyol and 1 to 15% by weight of moisture as a humectant. Further, it preferably contains 1 to 7% by weight of a surfactant, 0.01 to 15% by weight of a functional drug (stabilizer), sugars, liquid paraffin and the like. Furthermore, less than 0.05% of silicones can be included as a defoaming agent. Silicones are preferably used only as an antifoaming agent in order to promote a sticky feeling and should not be contained in the chemical solution in an amount of 0.05% by weight or more.

  Examples of the polyol 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. Including. In particular, when the main component is a polyhydric alcohol such as glycerin or propylene glycol, it is preferable in terms of manufacturability because the viscosity of the chemical solution and the coating amount are easily stabilized.

On the other hand, examples of the functional chemical include softeners, inorganic and organic fine particle powders, and the like.
The softening agent and the surfactant impart flexibility to the tissue and have an effect of smoothing the surface, and an anionic surfactant, a cationic surfactant and a zwitterionic surfactant 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 chemical solution, one of a hydrophilic polymer gelling agent, collagen, hydrolyzed collagen, hydrolyzed keratin, hydrolyzed silk, hyaluronic acid or a salt thereof, ceramide, etc. as a chemical solution that helps or maintains the moisture retention of polyol. A moisturizing agent such as any combination can be added.
Moreover, emollients, such as a fragrance | flavor and various natural extracts, vitamins, an emulsifier which stabilizes a compounding ingredient, an antifungal agent, and an organic acid can be blended as a functional chemical solution. Furthermore, you may contain the antioxidant of vitamin C and vitamin E.

  Here, the drug content in the moisturizing tissue according to the present invention indicates the content of a chemical 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, the content of components other than moisture in the applied chemical solution is shown. 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.

On the other hand, in the moisturizing tissue according to the present invention, when the chemical solution is applied to the tissue base paper, the amount of the chemical solution applied is appropriately adjusted so as to be the content of the drug. Specifically, the chemical solution may be applied in an amount of about 1.0 to 15% by weight, and about 10% more than the above drug content. That is, in the present invention, a chemical solution containing moisture may be applied to the tissue base paper at 2.2 to 6.6 g / m ² . The moisture content in the chemical solution is determined by the Karl Fischer method.
The chemical solution application amount can be calculated from the difference between the rice basis weight of the sheet that is laminated with the tissue base paper when the chemical solution is not applied to make two plies and the sheet basis weight immediately after the corresponding application. That is, it can be calculated by the following formula.
(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)

  Moreover, the moisturizing tissue according to the present invention has a two-ply structure as described above. Therefore, it is preferable that the coating is contained in the form applied to each outer surface of the laminate so that the crepe extension and the moisturizing effect are sufficiently exhibited by the chemical solution application on both sides. The chemical solution application amount in this embodiment is the total of the application amount per unit area of the plyed tissue paper sheet, and the application amount of each sheet is added.

Here, the viscosity of the chemical at the time of application is preferably 1 to 700 mPa · s at 40 ° C. because high speed processing can be performed. In particular, it is set to 50 to 400 mPa · s. When it is less than 1 mPa · s, when the chemical solution is applied by printing application using an anilox roll, a printing plate roll, a gravure roll, etc., the chemical solution is easily scattered on the roll. It becomes difficult to control the coating amount on the continuous sheet.
The temperature at the time of chemical solution application is preferably 30 ° C to 60 ° C, preferably 35 ° C to 55 ° C.

  Here, the chemical application rate of the moisturizing tissue according to the present invention is 7.0 to 20.0%. The drug application rate is defined as the moisture content in a chemical solution contained in a tissue paper product having a predetermined mass, with the moisture retention tissue having a predetermined mass adjusted under JIS P 8111 (1998) as the denominator (A) (g). The ratio of (B) divided by (A) is expressed as (%), with the removed mass (B) (g) as a molecule. (Drug content%) = (B) ÷ (A) × 100 (%)

On the other hand, the moisturizing tissue according to the present invention has a drug-containing density of 20.0 to 45.0 mg / cm ³ . The drug content density is the drug content (mg) per unit volume (cm ³ ) of two-ply tissue paper in the standard state of JIS P 8111 (1998).

〔Moisture percentage〕
On the other hand, the moisture retention tissue according to the present invention has a moisture content of 9.0 to 13.0%. This moisture content is determined based on JIS P 8127. That is, it calculates | requires by the following formula.
Moisture content (%) = {(weight of paper before drying) − (weight of paper after drying)} / (weight of paper before drying) × 100
In the present invention, as described above, by applying a predetermined amount of the above chemical solution to the tissue base paper according to the present invention in the above-described manner, the moisture absorption effect by the moisturizing agent is exhibited, and the moisture content can be obtained. In addition, when the moisture content is less than 9.0%, the moist feeling and the softness are inferior, and when it exceeds 13.0%, a sticky feeling is felt.

[Softness]
On the other hand, the moisturizing tissue according to the present invention has a softness value of 1.1 to 1.8 cN / 100 mm. The softness is measured based on a handle ohm method according to JIS L1096 E method. However, the test piece is 100 mm × 100 mm in size, and the clearance is 5 mm. The measurement is performed 5 times each in the vertical direction and the horizontal direction with 1 ply, and the average value of all 10 times is represented by 2 digits of decimal point and expressed in units of cN / 100 mm. When the softness value is out of the above range, the softness becomes difficult to feel.

[US tsubo]
On the other hand, the moisturizing tissue according to the present invention has a rice basis weight per sheet layer of 12 to 25 g / m ² , preferably 13 to 16 g / m ² . If the rice tsubo is less than 12 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).

[Paper thickness]
The paper thickness of the moisturizing tissue according to the present invention is 100 to 160 μm, particularly preferably 120 to 140 μm in a 2-ply state. In particular, when the thickness is 120 to 140 μm, a sufficient strength is ensured, the softness and smoothness are excellent, and there is no stickiness. In addition, when the paper thickness is less than 100 μm, it is preferable from the viewpoint of improving softness, but it is difficult to appropriately ensure the strength as the tissue paper. On the other hand, when the thickness exceeds 160 μm, the texture of the tissue paper is deteriorated and a feeling of roughness is generated during use.
Here, the paper thickness is measured using a dial thickness gauge (thickness measuring instrument) “PEACOCK G type” (manufactured by Ozaki Mfg. Co., Ltd.) under the same conditions after conditioning the test piece according to JIS P 8111 (1998). It shall be measured in the state of 2 plies. 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.

[Dry tensile strength]
On the other hand, the moisture retention tissue according to the present invention has a dry tensile strength (lateral) of 80 to 140 cN / 25 mm, preferably 80 to 120 cN / 25 mm. The dry tensile strength is measured in a 2-ply state. The measurement is performed according to the tensile test method of JIS P 8113 (1998). Among them, it shall be cut into a width of 25 mm in the horizontal direction under the standard conditions specified in JIS P 8111 (1998).
In the moisturizing tissue according to the present invention, when the dry tensile strength (horizontal) is 80 cN / 25 mm, the moisture retaining tissue is easily broken especially when the pop-up is pulled out in the direction from the storage box. In the moisturizing tissue according to the present invention, the ratio of MD direction (vertical) / CD direction (horizontal) is 3.4 to 4.0.

(Wet tensile strength)
On the other hand, the moisturizing tissue according to the present invention has a wet tensile strength (lateral) of 50 to 70 cN / 25 mm. The wet tensile strength is measured in a 2-ply state. The measurement is performed according to JIS P 8135 (1998). In the moisturizing tissue according to the present invention, when the wet tensile strength (horizontal) is 50 cN / 25 mm, it is difficult to secure sufficient strength particularly when the facial care or nose is bitten.

[Static friction coefficient]
On the other hand, the moisture retention tissue according to the present invention has a coefficient of static friction of 0.53 to 0.68, more preferably 0.55 to 0.65. The static friction coefficient here is measured by the following method according to JIS P 8147 (1998).
First, the moisturizing tissue is peeled off in one ply and attached to the acrylic flat plate so that the surface that was on the outer surface of the laminate at the time of two plies becomes the outer side (outer surface). Then, a moisturizing tissue different from the tissue paper is wound around the weight of 100 g with 2 plies so as to cover it, and placed on the 1 ply moisturizing tissue on the acrylic flat plate. Next, the acrylic flat plate is tilted, and the angle at which the weight around which the tissue paper is wound slides is measured. The angle measurement is performed 8 times in total for each of the MD directions and the CD directions of the moisturizing tissue for a total of 8 times to calculate an average angle, and the tangent value is defined as a static friction coefficient. Within the range of the static friction coefficient of the present invention, smoothness and stickiness are excellent.

〔Growth rate〕
On the other hand, the moisturizing tissue according to the present invention desirably has an MD (longitudinal) elongation of 11.0 to 15.0%. If the elongation is less than 11.0%, it tends to be torn, and if it exceeds 15.0%, the wiping operation becomes difficult. In addition, elongation rate is measured using Minebea Co., Ltd. "universal tension compression testing machine TG-200N". The elongation is the “stretch at break” described in “3. Definition e) of JIS P 8113.

[MMD]
Here, it is desirable that the moisturizing tissue in the present invention has an MMD (average deviation of friction coefficient μ (unit: dimensionless)), which is a conventional smoothness index, of 8.5 or less. As a method for measuring the MMD value, as shown in FIG. 11A, the contact surface of the friction element 112 is measured by applying a tension of 20 g / cm in a predetermined direction (downwardly rightward in FIG. 11A). While making contact with the surface of tissue paper 111 as a sample at a contact pressure of 25 g, the sample 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). Is 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. 11 (a) schematically shows the friction element 112, and FIG. 11 (b) shows an enlarged view of a portion surrounded by a one-dot chain line in FIG. 11 (a).

[Product density]
On the other hand, the moisturizing tissue is folded so as to be a pop-up type by an interfolder, and is cut into a product size at any stage before and after the folding process, for example, 180 sets are boxed into products. However, the moisture retention tissue according to the present invention has a density (product density) of 180 sets after folding of 0.15 to 0.25 g / cm ³ , particularly 0.17 to 0.23 g / m ³ . There should be. When it is lower than 0.15 g / cm ³ , moist feeling and smoothness are not obtained, and when 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 paper density is the paper thickness (D) of tissue paper (2 ply) according to “PEACOCK G type”, which is a value (C) that is twice the weight of the tissue paper product 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))

“First example of manufacturing moisturizing tissue: Example of manufacturing method by applying ply machine”
The moisturizing tissue of the present invention described above can be manufactured, for example, as follows.
First, in the papermaking facility, a tissue base paper having a crepe is wound to produce primary raw rolls 11 and 12 (also generally referred to as jumbo rolls).

  Next, two primary raw rolls are set in a ply machine integrated with the coating apparatus shown in FIG. 1, and continuous tissue base papers 31 and 32 are wound from each primary raw roll, and are laminated by the laminating roller 13. Ply. Thereafter, calendar processing may be performed by the ply machine calendar 14 as necessary. Each tissue base paper (hereinafter also referred to as a continuous sheet) that has been made into two plies is sent to the chemical solution application step to apply the chemical solution.

As a method for applying a chemical solution, a known application method such as application by roll transfer such as spray application, flexo application, and gravure application can be employed. However, preferably, it is a printing method such as gravure coating, flexographic coating, etc. that can apply a chemical solution evenly over the entire coating surface. Especially when a flexographic printing machine equipped with a doctor chamber 15 is used, a chemical solution with a stable coating amount. Can be supplied.
In the ply machine (ply process) of FIG. 1, two flexo coaters 16 and 17 are provided, and a chemical solution is applied to each side of a two-ply continuous sheet.

In addition, when using a flexographic printing system as a chemical | medical solution application means, a processing speed shall be 100-1100 m / min, Preferably it is 350-1050 m / min, Most preferably, you may be 450-1000 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.
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.

  On the other hand, 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.

  The continuous sheet after applying the chemical solution is supplied to the contact embossing roller 18 and the roller roll 19 and laminated and integrated by applying a contact embossing (knurling) process to the two-ply continuous sheet. However, the lamination and integration of the tissue base papers is not limited to that by contact embossing. In addition, when providing a difference in a chemical | medical solution application amount on the front and back, it is good to make a continuous sheet with few application amounts contact a contact embossing roller. The subsequent winding process is improved.

When providing contact embossing, it is preferable to apply it 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. Each tissue base paper is difficult to peel off when made into a product.
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 the illustrated embodiment, the chemical solution is applied before contact embossing. However, the chemical solution may be applied after contact embossing.

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.
However, when the moisturizing tissue of the present invention is packaged into a product, it is particularly suitable to adopt a folding process with a multi-stand type interfolder from the viewpoint of the structure and productivity of the moisturizing tissue of the present invention. . The folding process in the multi-stand type interfolder will be described below.
In the multi-stand type inter, a large number of secondary web rolls 22 manufactured by the above-described ply machine are set, and secondary paper rolls are drawn out from the set secondary web rolls 22 to be folded and laminated, thereby stacking tissue paper bundles. Is manufactured. 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 web roll R has a slit in the tissue paper width, and is wound and set in multiple widths of tissue paper, in the example shown, 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 by the multi-stand type interfolder 6 as described above is cut (cut) at a predetermined interval in the flow direction FL by the subsequent cutting means 66 and is substantially cut. The tissue paper bundle 67a is a rectangular parallelepiped tissue paper bundle 67a. As shown in FIG. 10 (a), this tissue paper bundle 30a is further accommodated in a storage box B having a rectangular parallelepiped shape and having a take-out port on the upper surface in the subsequent equipment. In the multi-stand type interfolder 1 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 ( 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.
The moisturizing tissue according to the present invention has a particularly effective structure in terms of the specification mode of the product in the drawing direction.

  When folding is performed using a rotary interfolder, the longitudinal direction (MD direction) is along the folding direction of the tissue paper, and the lateral direction (CD is along the direction orthogonal to the folding direction of the tissue paper. Direction), and in the product, the tissue paper is drawn out along the vertical direction.

"Second manufacturing example: Example of manufacturing method by off-machine coating"
The moisturizing tissue according to the present invention may be manufactured by using a chemical liquid application device different from the ply machine in addition to the ply machine application shown in the first manufacturing example. When performing off-machine chemical application, the ply process is performed using a ply machine as shown in FIG. That is, the continuous sheets 31 and 32 are unwound from the primary fabric rolls 11 and 12 and laminated by the laminating roller 13 to form two plies, and then supplied to the contact embossing roller 18 and the roller roll 19 without passing through the chemical solution coating process. A 2-ply continuous sheet provided with embossing is wound up by a winding roll 221 while the chemical solution is not applied, and a secondary raw roll (not applied with a chemical solution) 222 is obtained.

Next, in this production example, the secondary raw roll is supplied to an off-machine chemical solution coating apparatus different from the ply machine.
The ply machine can be operated at 100 to 1100 m / min. However, when a rotary interfolder described later is used for folding, the current speed is to operate at 80 to 100 m / min because the operation speed of the interfolder is rate limiting.

  The off-machine coating apparatus is not particularly limited, but a flexographic printing method is suitable as in the on-line. In the example shown in FIG. 13, the chemical solution is applied to the secondary continuous sheet fed from the secondary raw roll 222 by a flexo coater 216 provided with a doctor chamber 215. In the illustrated example, the chemical solution is applied only to one side of a two-ply secondary raw sheet, but it may of course be applied to both sides. The sheet after applying the chemical solution is wound up by a winding drum 224 to form a tertiary raw roll 223. The tertiary material roll is supplied to a rotary interfolder and subjected to folding. In addition, after cutting a sheet | seat after chemical | medical solution application | coating to a product width through a slitter, you may wind up and make it into a tertiary original fabric roll, and you may fold by a multi-stand type interfolder.

In order to confirm the effect of the present invention, Table 1 shows the results of evaluating the paper quality of the products of Examples and Comparative Examples according to the present invention.
Examples 1 to 5 are moisturizing tissues according to the present invention, and folding was performed using a multi-stand type interfolder.
Comparative Examples 1 to 4 are those in which the contents of the wet paper strength agent and the sizing agent in the tissue base paper are outside the scope of the present invention, Comparative Example 5 is a non-moisturizing general-purpose tissue paper, and Comparative Example 6 is a conventional one. Moisturizing lotion type tissue papers, Comparative Examples 7 and 8 are non-humidifying type high-grade tissue papers having a large weight and a large paper thickness. In addition, the physical properties, composition, and specifications in each example are as shown in Table 1.
The measuring methods of rice tsubo, paper thickness, tensile strength, elongation rate, softness, static friction coefficient, and moisture content are as described in the section of the embodiment for carrying out the invention. The drug content indicates the ratio of the dry weight of the drug solution to the tissue weight of the tissue paper.
In addition to the evaluation of paper quality, sensory evaluation based on the following criteria was performed for softness, smoothness, thickness, and moistness for each of 30 subjects. 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 standard, 2: Inferior, 1: Notably inferior Furthermore, the chemical-coated tissue paper was also evaluated for the presence or absence of stickiness.
○: Little sticky feeling ×: Clearly sticky feeling

The moisturizing tissue of the example according to the present invention has a higher wet tensile strength in the CD direction than Comparative Examples 1 to 3. Further, it is shown that the softness and static friction coefficient are lower than those of commercially available Comparative Examples 5 to 8, and the paper quality is smooth and soft.
Further, in the 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 has a stickiness found in a moisturizing tissue. It was found that the feeling was reduced.

  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.

  Further, when comparing the tissue paper according to the present invention and the comparative examples 1 to 4 in which the amounts of the wet paper strength agent and the sizing agent in the tissue base paper are different, in the comparative example 1 having a small amount of the wet paper strength agent, there is a see-through. The results were inferior to those of the general-purpose tissue type of Comparative Example 5, and Comparative Example 2 with a large amount of wet paper strength agent resulted in extremely poor moisture absorption. As for the sizing agent, Comparative Example 3 with a small amount of sizing agent results in poor wiping resistance and moisture penetration, and Comparative Example 4 with a large amount of sizing agent is insufficient in softness and smoothness. As a result.

  As described above, the structure of the moisturizing tissue according to the present invention suppresses the sticky feeling seen in the conventional moisturizing tissue and has a softness, smoothness, and moist feeling equal to or higher than those of the moisturizing tissue. In addition, it was shown that it can be used suitably without breaking even in usage modes involving excessive water absorption, such as wiping liquids, and excellent versatility,

  DESCRIPTION OF SYMBOLS 1 ... Multi stand type interfolder, 11 ... Primary material roll, 12 ... Primary material roll, 15 ... Doctor chamber, 16 ... Flexo coater, 17 ... Flexo coater, 20 ... Slitter, 21 ... Winding drum, 22 ... Original material Roll, 60 ... Folding mechanism part, 63 ... Secondary continuous sheet, 65 ... Conveyor, 67 ... Laminated belt, 112 ... Friction element, 215 ... Doctor chamber, 216 ... Flexo coater, 222 ... Secondary fabric roll, 223 ... Tertiary roll, 300 ... Rotary interfolder.

Claims (2)

A moisturizing tissue paper product in which a two-ply moisturizing tissue paper containing a chemical containing a moisturizing agent is folded in a pop-up manner and stored in a substantially rectangular parallelepiped storage box,
In the moisturizing tissue paper product, the storage box is formed of a paper box having an opening on the upper surface parallel to the long side direction, and the opening is covered with a film attached to the inner surface of the storage box, and the film is long in the opening. It has a slit parallel to the side direction, the pulling direction when pulling out the moisturizing tissue paper from the storage box is a lateral direction, and
The moisturizing tissue paper
The tissue base paper contains 7.0-22.0 kg / t of wet paper strength agent and 1.0-8.0 kg / t of sizing agent,
The chemical solution contains a polyol and a functional drug containing an oil component,
The drug content of the drug solution is 2.0 to 6.0 g / m ² ,
The moisture content is 9.0-13.0%,
The basis weight per layer of the sheet constituting the two plies is 12 to 25 g / m ² ,
2-ply paper thickness is 100-160 μm,
The softness is 1.1 to 1.8 cN / 100 mm,
The dry tensile strength (lateral) is 80 to 140 cN / 25 mm,
Wet tensile strength (lateral) is 50 to 70 cN / 25 mm,
The ratio of dry tensile strength (longitudinal) / dry tensile strength (lateral) is 3.4 to 4.0 ,
The static friction coefficient measured by the following procedures (A) to (D) is 0.53 to 0.68.
Moisturizing tissue paper product characterized by that.
(A) The moisturizing 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 moisturizing tissue paper at the time of two plies becomes the outside.
(B) A moisturizing tissue paper different from the moisturizing tissue paper is wound around a 100 g weight with 2 plies and placed on the moisturizing 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 MD direction of the moisturizing tissue paper and in the CD direction of the moisturizing tissue paper, and the average angle is calculated by measuring 8 times in total, 4 times each. Is the coefficient of static friction. It is a manufacturing method of the moisture retention tissue paper of Claim 1,
A tissue produced by adding 7.0 to 22.0 kg / t of a wet paper strength agent and 1.0 to 8.0 kg / t of a sizing agent in an absolutely dry amount of active ingredients in a papermaking raw material, and making a paper with a crepe rate of 10 to 30%. After laminating two layers of base paper, a chemical solution containing 70 to 90% by weight of polyol, 1.0 to 15% by weight of water, and 0.01 to 15% by weight of a functional drug containing an oily component is 2.2 to 2% on both sides. 6.6 g / m ^{2 is} applied,
The manufacturing method of the moisture retention tissue paper characterized by the above-mentioned.

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