WO2017169416A1 - Production device for sanitary tissue paper and production method for sanitary tissue paper - Google Patents

Production device for sanitary tissue paper and production method for sanitary tissue paper Download PDF

Info

Publication number
WO2017169416A1
WO2017169416A1 PCT/JP2017/007309 JP2017007309W WO2017169416A1 WO 2017169416 A1 WO2017169416 A1 WO 2017169416A1 JP 2017007309 W JP2017007309 W JP 2017007309W WO 2017169416 A1 WO2017169416 A1 WO 2017169416A1
Authority
WO
WIPO (PCT)
Prior art keywords
microcapsule
sanitary thin
paper
thin paper
microcapsules
Prior art date
Application number
PCT/JP2017/007309
Other languages
French (fr)
Japanese (ja)
Inventor
奨 与那覇
Original Assignee
大王製紙株式会社
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by 大王製紙株式会社 filed Critical 大王製紙株式会社
Publication of WO2017169416A1 publication Critical patent/WO2017169416A1/en

Links

Images

Classifications

    • AHUMAN NECESSITIES
    • A47FURNITURE; DOMESTIC ARTICLES OR APPLIANCES; COFFEE MILLS; SPICE MILLS; SUCTION CLEANERS IN GENERAL
    • A47KSANITARY EQUIPMENT NOT OTHERWISE PROVIDED FOR; TOILET ACCESSORIES
    • A47K10/00Body-drying implements; Toilet paper; Holders therefor
    • A47K10/16Paper towels; Toilet paper; Holders therefor
    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H21/00Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties
    • D21H21/14Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties characterised by function or properties in or on the paper
    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H21/00Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties
    • D21H21/50Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties characterised by form
    • D21H21/52Additives of definite length or shape
    • D21H21/54Additives of definite length or shape being spherical, e.g. microcapsules, beads

Definitions

  • the present invention relates to a thin paper containing a chemical solution containing a humectant and the like.
  • tissue paper As a sanitary thin paper is generally used to bite the nose.
  • the frequency of use increases, the oil content of the nasal epidermis is lost and rubbed. I feel pain.
  • lotion containing glycerin which is a moisturizing component, has been applied, and tissue papers that are smooth and have a smooth feel have been distributed (see, for example, Patent Document 1).
  • a tissue paper has been proposed in which a microcapsule having functionality such as a fragrance is added to the lotion to give a refreshing feeling and to relieve mental stress due to rhinitis or nasal congestion (see, for example, Patent Document 2).
  • the intensity of the scent In order to change the type and type, it is necessary to use another adjusted chemical solution, which requires replacement work, and therefore requires a great deal of labor and time, such as switching work and cleaning the equipment to be applied. It was.
  • the above-mentioned problem is not limited to tissue paper, but can be a problem that can occur with respect to the entire sanitary thin paper.
  • the purpose of the present invention is to improve the productivity of sanitary thin paper coated with microcapsules and lotion chemicals.
  • the invention according to claim 1 is a sanitary thin paper manufacturing apparatus, A microcapsule applicator for applying microcapsules to a sanitary thin paper base; A liquid application device for applying a lotion chemical solution to a sanitary thin paper base, The microcapsule coating apparatus applies the microcapsules to the base paper by electrostatic coating.
  • the invention according to claim 2 is the sanitary thin paper manufacturing apparatus according to claim 1
  • the liquid applying apparatus is a rotor dampening printing apparatus.
  • the invention according to claim 3 is the sanitary thin paper manufacturing apparatus according to claim 1 or 2
  • the microcapsules are characterized in that any one of urethane, urea-melamine, and urea-formalin is used as a main raw material.
  • a microcapsule application process for applying microcapsules to a sanitary thin paper base A liquid application process for applying a lotion chemical to a sanitary thin paper base, The microcapsule application step is characterized in that the microcapsules are applied to the base paper by electrostatic application.
  • Invention of Claim 5 is a manufacturing method of the sanitary thin paper of Claim 4, The liquid application process is performed by a rotor dampening printing method.
  • Invention of Claim 6 is a manufacturing method of the sanitary thin paper of Claim 4 or 5, The microcapsule coating step is characterized in that the microcapsule is mainly coated with any one of urethane, urea-melamine, and urea-formalin.
  • the sanitary thin paper manufacturing apparatus or manufacturing method of the present invention since it is not necessary to mix microcapsules into the lotion chemical solution, only the microcapsules to be applied need to be replaced even when adjusting the functionality of the microcapsules. Since the lotion chemical solution is not exchanged, the work load can be reduced and the work time can be reduced, and the productivity of sanitary thin paper can be improved.
  • FIG. 1 It is a schematic block diagram of the manufacturing apparatus of the sanitary thin paper which is embodiment of this invention. It is a block diagram which shows the detail of the microcapsule application
  • FIG. 1 is a schematic configuration diagram of a sanitary thin paper manufacturing apparatus according to an embodiment of the present invention.
  • This sanitary thin paper manufacturing apparatus 10 is a manufacturing apparatus whose main purpose is to apply lotion chemicals and microcapsules to a base paper of sanitary thin paper.
  • the base paper of the sanitary thin paper of the present invention is preferably a two-ply laminate of crepe paper having a basis weight of 10 to 18 g / m 2 according to JIS P 8124 (1998). Further, the paper thickness measured with a dial thickness gauge (thickness measuring instrument) “PEACOCK G type” (manufactured by Ozaki Mfg. Co., Ltd.) under the conditions of JIS P 8111 (1998) is 80 to 250 ⁇ m, preferably It is desirable that the thickness is 100 to 200 ⁇ m, more preferably 130 to 180 ⁇ m.
  • the longitudinal direction of dry tensile strength (hereinafter also referred to as dry paper strength) specified in JIS P 8113 (1998) is 200 to 700 cN / 25 mm, preferably 250 to 600 cN / 25 mm, particularly preferably 300 to 600 cN with 2 plies.
  • the lateral direction is 50 to 250 cN / 25 mm, preferably 80 to 220 cN / 25 mm, particularly preferably 100 to 200 cN / 25 mm with 2 plies. If the dry tensile strength is too low, troubles such as paper breakage and elongation at the time of production and use are likely to occur, and if it is too high, the touch becomes stiff during use.
  • tissue paper, toilet paper, paper towel, etc. are mentioned.
  • the pulp raw material is preferably composed of NBKP and LBKP.
  • Waste paper pulp may be blended as appropriate, but it is preferably composed only of NBKP and LBKP of virgin pulp because it is compatible with an aqueous lotion solution and desirable in terms of the resulting texture.
  • the lotion chemical is applied to the base paper of the sanitary thin paper.
  • the lotion solution is preferably applied to both sides of the base paper laminated on the two plies.
  • the application amount of the lotion chemical in the present invention is preferably in the range of 20 to 30% by weight of the base paper weight (US tsubo).
  • the lotion chemical solution contains water and a polyol. In particular, those containing 70 to 90% polyol and 10 to 20% water, particularly preferably 0.01 to 22% further containing a functional drug.
  • Such an aqueous chemical solution has an action of extending the crepe of the base paper, and improves the smoothness of the surface of the sanitary thin paper as well as the moisture retention.
  • the polyol includes polyhydric alcohols such as glycerin, diglycerin, propylene glycol, 1,3-butylene glycol, polyethylene glycol, and derivatives thereof, and saccharides 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 sanitary thin paper 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.
  • one or more of a hydrophilic polymer gelling agent, collagen, hydrolyzed collagen, hydrolyzed keratin, hydrolyzed silk, hyaluronic acid or a salt thereof, ceramide, etc. are optionally selected as agents that maintain the moisture retention of polyol.
  • a moisturizer such as a combination of the above can be added.
  • emollients such as fragrances and various natural extracts, vitamins, emulsifiers that stabilize compounding ingredients, antifoaming agents, antifungal agents, organic acids, etc., that suppress foaming of lotion chemicals and stabilize application as functional agents. Can be blended.
  • the main component is a polyhydric alcohol such as glycerin or propylene glycol, it is preferable from the viewpoint of application in terms of stabilizing the viscosity and application amount of the lotion chemical.
  • microcapsules applied to sanitary thin paper On the other hand, in this invention, a microcapsule is apply
  • the microcapsules of the present invention are preferably suitable for electrostatic coating by the microcapsule coating apparatus 40 of the sanitary thin paper manufacturing apparatus 10 described later.
  • Microcapsules contain perfume. As materials for such microcapsules, those mainly composed of urethane, urea-melamine, urea-formalin, agar, and gelatin can be used. However, since the microcapsules are exposed to lotion chemicals, Urethane, urea-melamine, and urea-formalin are more preferable. In addition, since the microcapsule is scraped off by the doctor blade 44 in the microcapsule coating apparatus 40 of the manufacturing apparatus 10 to be described later, it is desirable to design the microcapsule so as to withstand the scraping.
  • the film thickness of the microcapsule is not particularly limited, but is generally 0.1 to 1.0 ⁇ m, preferably 0.1 to 0.5 ⁇ m.
  • the average particle size of the perfume-containing microcapsules 32 m is preferably 10 to 50 ⁇ m. If it is this range, the fragrance
  • a menthol-based fragrance containing a cooling agent and l-menthol is used as a fragrance included in the microcapsule.
  • This fragrance gives the skin an excellent cooling feeling due to the volatility and cooling agent of menthol when biting the nose.
  • the sanitary thin paper manufacturing apparatus 10 includes a base paper supply device 20 that holds a roll of base paper P and feeds the base paper, and a microcapsule application device 40 that applies microcapsules to the base paper P.
  • the liquid application device 30 for applying the lotion chemical solution to the base paper P and the laminating device 60 for stacking the base paper P while being folded are provided.
  • the base paper P of sanitary thin paper as a pre-stage of the production apparatus 10, first, a thin paper is made from pulp fibers (preferably 100% virgin pulp fiber not containing waste paper pulp) in a paper making apparatus, and crepe is applied if necessary. After the calendar treatment, this is wound up to produce a primary raw roll (generally also referred to as a jumbo roll). Then, although not shown, this primary raw roll is set in a known ply machine, The primary continuous sheet fed from the primary raw roll is superposed and wound, and is cut into a plurality of pieces (divided into a plurality of parts in the width direction) to produce a secondary raw roll made of a plurality of plies.
  • pulp fibers preferably 100% virgin pulp fiber not containing waste paper pulp
  • the base paper supply device 20 rotatably holds two secondary raw rolls 21 manufactured by a ply machine, and feeds a secondary continuous sheet from each secondary raw roll as base paper P.
  • the base paper supply device 20 includes a transport roller 22 that individually transports the base paper P fed from each secondary raw roll 21, and a tension roller 23 provided in the middle of each transport path formed by each transport roller 22. And.
  • the tension roller 23 is for controlling the tension applied to the base paper P transported by the transport roller 22.
  • the microcapsule coating apparatus 40 applies microcapsules to the base paper P without mixing it into the lotion chemical solution, and applies two microcapsules to one side of each base paper P transported by two routes.
  • a coating unit 41 is provided. As shown in FIG. 2, each coating unit 41 has a microcapsule reservoir 42 filled with microcapsules and an upper portion of the outer peripheral surface exposed to the microcapsules arranged and filled below the microcapsule reservoir 42.
  • the lower part of the microcapsule storage part 42 is widely opened, and the spraying roller 43 is arranged so as to close the opening part.
  • the upper part of the outer peripheral surface of the spraying roller 43 is exposed to the microcapsules filled in the microcapsule storage part 42, and the spraying roller 43 rotates so that the entire circumference of the outer peripheral surface is microscopic.
  • the capsule adheres.
  • the doctor blade 44 is provided on the upstream side and the downstream side in the conveying direction of the base paper P with respect to the spreading roller 43, respectively, and the microcapsules attached to the outer peripheral surface of the spreading roller 43 that rotates are made to have a uniform thickness. Thin layer.
  • the two anti-scattering rollers 45 rotate in sliding contact with the spraying roller 43.
  • a microcapsule spraying region surrounded by the spraying roller 43 and the two scattering prevention rollers 45 is formed below the spraying roller 43.
  • the base paper P is conveyed in the state which left a little clearance gap with respect to the lower part of the outer periphery of the two scattering prevention rollers 45.
  • the discharge line 46 slidably contacting the spraying roller 43 and the two scattering prevention rollers 45 in the microcapsule spraying area removes power, so that the microcapsules are outer peripheral surfaces of the spreading roller 43 and the two scattering prevention rollers 45. Is scraped off and falls to the base paper P side.
  • the charger 47 disposed on the lower side of the base paper P is in a charged state, the microcapsules in the microcapsule spraying area are attracted to the base paper P side. Application can be performed.
  • the liquid coating apparatus 30 includes a total of four coating units 31 for each base paper P transported in two routes, one for applying lotion chemical on the front side and one for applying lotion chemical on the back side.
  • the coating unit 31 has a configuration as a rotor dampening printing type rotor dampening printing device, and is disposed opposite to a sprayer 32 for spraying a lotion chemical solution, in front of the sprayer 32, and a base paper P is placed on the outer peripheral surface thereof.
  • a back roller 33 that is conveyed along the back roller 33 is applied, and a lotion chemical is applied to the base paper P conveyed by the back roller 33 by the sprayer 32.
  • the laminating apparatus 60 includes two embossing rollers 61 that individually emboss each base paper P conveyed by two routes, and a stacking unit 62 that stacks the base papers P while being folded. Since these are the same as well-known ones, detailed description thereof is omitted.
  • FIG. 3 is an explanatory view showing the manufacturing process of sanitary thin paper in order.
  • a method for manufacturing sanitary thin paper using the manufacturing apparatus 10 will be described with reference to FIGS.
  • each base paper P is coated with a microcapsule on one side by an individual coating unit 41 in a microcapsule coating apparatus 40. Since the microcapsule coating apparatus 40 performs electrostatic coating, the microcapsules adhere to the plane of the base paper P by electrostatic force (FIG. 3B: microcapsule coating process). In addition, the code
  • each base paper P is applied with a lotion solution on both sides thereof by the respective application units 31 arranged on both sides of the transported base paper P in the liquid application device 30 (FIG. 3C: liquid application step).
  • the applied lotion solution penetrates inside the base paper P.
  • symbol 1 in FIG. 3C shows a lotion chemical
  • each base paper P is embossed by each embossing roller 61 in the laminating apparatus 60, and further folded and stacked by the laminating unit 62 (lamination process).
  • the base paper P folded and laminated in this manner is finally cut at an interval of the same width as the product width in the subsequent equipment, and becomes a product (sanitary thin paper) through processing such as boxing and packaging. .
  • the sanitary thin paper manufacturing apparatus 10 includes a microcapsule applicator 40 that applies microcapsules to the base paper P in a separate process from the liquid applicator 30, and a liquid applicator 30 that applies a lotion chemical to the base paper P. Therefore, the microcapsule application process and the liquid application process are performed in separate processes. For this reason, unlike the case where microcapsules are mixed and applied in a lotion chemical solution, adjustment of the functionality of the microcapsules, for example, even when changing the intensity or type of fragrance, only the microcapsules to be applied need to be replaced. Since the chemical solution is not exchanged, it is possible to reduce the work load and the work time, and it is possible to improve the productivity of sanitary thin paper. In addition, the manufacturing apparatus 10 having the above-described configuration can be realized only by adding the microcapsule coating apparatus 40 to a conventional sanitary thin sheet manufacturing apparatus that applies a lotion chemical solution and does not apply microcapsules. Can be achieved.
  • the microcapsule coating apparatus 40 of the manufacturing apparatus 10 includes the discharge unit 46 and the charger 47, and the microcapsule is applied to the base paper P by electrostatic coating. It can be performed by coating. This makes it possible to effectively prevent the microcapsules from becoming dust and diffusing around when applying the microcapsules, while making it unnecessary to mix the microcapsules into the lotion chemical.
  • the liquid application apparatus 30 of the manufacturing apparatus 10 is a rotor dampening printing apparatus
  • the lotion chemical can be applied by a rotor dampening printing method in the liquid application process. This makes it possible to apply with a simple configuration without using a specially shaped roller with grooves and ridges for supplying lotion chemicals to the base paper, such as gravure printing and flexographic printing. Become.
  • a microcapsule to be applied in the microcapsule application step uses a material mainly made of urethane, urea-melamine, or urea-formalin. If it is a microcapsule which uses these as a main material, even if it exposes to a lotion chemical
  • liquid application process by the liquid application apparatus 30 of the manufacturing apparatus 10 is not limited to the rotor dampening method.
  • other liquid application methods such as a flexographic printing method, a roll transfer method, an ink jet method, a spray method, and a gravure printing method may be used.
  • the microcapsule coating process by the microcapsule coating apparatus 40 is not limited to electrostatic coating.
  • other powder coating methods such as electrostatic spraying and spraying may be applied to the microcapsules.
  • electrostatic spraying and spraying may be applied to the microcapsules.
  • the microcapsules are not limited to those suitable for electrostatic coating, and microcapsules made of a wider range of materials can be used.
  • flavor was utilized was illustrated, the microcapsule which encloses another functional component may be utilized.
  • Examples 1 and 2 and Comparative Examples 1 to 3 Various two-ply tissue papers (Examples 1 and 2 and Comparative Examples 1 to 3) shown in the chart of FIG. 4 were produced, and the lotion solution and the fragrance capsule described in the table were applied, and the operability and sensory evaluation were performed. It was.
  • the lotion chemical solution was applied at 5.6 g / m 2
  • the fragrance capsule (microcapsule) having an average particle diameter of 10 ⁇ m was applied at 0.60 g / m 2 .
  • a fragrance capsule powder microcapsule
  • a lotion chemical was applied by a gravure method.
  • Example 2 a fragrance capsule powder (microcapsule) was applied by an electrostatic device, and then a lotion chemical was applied by a spray method.
  • Comparative Example 1 a chemical solution in which a fragrance capsule (microcapsule) was mixed in a lotion chemical solution was subjected to gravure coating. At that time, no electrostatic device is used.
  • Comparative Example 2 a lotion chemical was applied by a gravure method, and then a fragrance capsule (microcapsule) was dispersed in water and sprayed. At that time, no electrostatic device is used.
  • Comparative Example 3 a lotion chemical solution was applied by a gravure method, and then a perfume capsule (microcapsule) was dispersed in water for gravure coating. At that time, no electrostatic device is used.
  • Example 1 and Example 2 according to the present invention differ from Comparative Examples 1 to 3 in that they exhibit excellent softness and fragrance strength, and there is no residual scent of equipment. Switching time has been shortened.
  • the present invention can be suitably used in the field of manufacturing thin paper.

Abstract

The present invention comprises: a microcapsule coating device 40 that coats microcapsules on a base paper P for sanitary tissue paper; and a liquid coating device 30 that coats a lotion solution on to the base paper P for the sanitary tissue paper. The microcapsule coating device coats microcapsules on to the base paper by using electrostatic coating. As a result, coating whereby microcapsules are mixed into the lotion solution is avoided and, during microcapsule function adjustment, lotion solution replacement work is avoided and the workload and work time are reduced thereby improving workability.

Description

衛生薄葉紙の製造装置及び衛生薄葉紙の製造方法Sanitary tissue paper manufacturing apparatus and sanitary tissue paper manufacturing method
 本発明は、保湿剤等を含む薬液を含有する薄葉紙に関するものである。 The present invention relates to a thin paper containing a chemical solution containing a humectant and the like.
 風邪や花粉症などが原因で鼻水が出る場合には、鼻をかむために衛生薄葉紙としてのティッシュペーパーが一般に使用されるが、その使用頻度が高くなると、鼻の表皮の油分が失われてこすれによる痛みを感じるようになる。このため、近年は、保湿成分であるグリセリン等を含んだローションが塗布され、滑性が良く、肌触りが滑らかなティッシュペーパーが流通している(例えば、特許文献1参照)。
 また、香料等の機能性を有するマイクロカプセルをローションに加えることにより、清涼感を与えて鼻炎や鼻づまりによる精神的なストレス緩和を図るティッシュペーパーも提案されている(例えば、特許文献2参照)。
When a runny nose occurs due to a cold or hay fever, tissue paper as a sanitary thin paper is generally used to bite the nose. However, when the frequency of use increases, the oil content of the nasal epidermis is lost and rubbed. I feel pain. For this reason, in recent years, lotion containing glycerin, which is a moisturizing component, has been applied, and tissue papers that are smooth and have a smooth feel have been distributed (see, for example, Patent Document 1).
In addition, a tissue paper has been proposed in which a microcapsule having functionality such as a fragrance is added to the lotion to give a refreshing feeling and to relieve mental stress due to rhinitis or nasal congestion (see, for example, Patent Document 2). .
特表2007-534386号公報Special table 2007-534386 特開2013-78373号公報JP 2013-78373 A
 上述のようにローションにマイクロカプセルを添加した薬液を塗布したティッシュペーパーにおいては、マイクロカプセルによる機能性の調整を行う場合、例えば、マイクロカプセルが香料を内包したものである場合には、香りの強度や種別を変更するためには、調整された別の薬液を使用しなければならず、交換作業が必要となるため、切り替え作業や塗布する設備の洗浄等、多大な労力と時間が必要となっていた。
 なお、上記の問題は、ティッシュペーパーに限らず、広く衛生薄葉紙全体について生じ得る問題である。
As described above, in the tissue paper coated with the chemical solution in which the microcapsule is added to the lotion, when adjusting the functionality by the microcapsule, for example, when the microcapsule contains a fragrance, the intensity of the scent In order to change the type and type, it is necessary to use another adjusted chemical solution, which requires replacement work, and therefore requires a great deal of labor and time, such as switching work and cleaning the equipment to be applied. It was.
The above-mentioned problem is not limited to tissue paper, but can be a problem that can occur with respect to the entire sanitary thin paper.
 本発明は、マイクロカプセルとローション薬液とが塗布された衛生薄葉紙の生産性の向上を図ることをその目的とする。 The purpose of the present invention is to improve the productivity of sanitary thin paper coated with microcapsules and lotion chemicals.
 以上の課題を解決するため、請求項1に記載の発明は、衛生薄葉紙の製造装置において、
 衛生薄葉紙の原紙に対してマイクロカプセルを塗布するマイクロカプセル塗布装置と、
 衛生薄葉紙の原紙に対してローション薬液を塗布する液体塗布装置とを備え、
 前記マイクロカプセル塗布装置は、前記マイクロカプセルを静電塗布により前記原紙に塗布することを特徴とする。
In order to solve the above problems, the invention according to claim 1 is a sanitary thin paper manufacturing apparatus,
A microcapsule applicator for applying microcapsules to a sanitary thin paper base;
A liquid application device for applying a lotion chemical solution to a sanitary thin paper base,
The microcapsule coating apparatus applies the microcapsules to the base paper by electrostatic coating.
 請求項2に記載の発明は、請求項1に記載の衛生薄葉紙の製造装置において、
 前記液体塗布装置は、ローターダンプニング印刷装置であることを特徴とする。
 請求項3に記載の発明は、請求項1又は2記載の衛生薄葉紙の製造装置において、
 前記マイクロカプセルは、ウレタン、尿素-メラミン、尿素-ホルマリンのいずれかを主たる原料とすることを特徴とする。
The invention according to claim 2 is the sanitary thin paper manufacturing apparatus according to claim 1,
The liquid applying apparatus is a rotor dampening printing apparatus.
The invention according to claim 3 is the sanitary thin paper manufacturing apparatus according to claim 1 or 2,
The microcapsules are characterized in that any one of urethane, urea-melamine, and urea-formalin is used as a main raw material.
 請求項4に記載の発明は、衛生薄葉紙の製造方法において、
 衛生薄葉紙の原紙に対してマイクロカプセルを塗布するマイクロカプセル塗布工程と、
 衛生薄葉紙の原紙に対してローション薬液を塗布する液体塗布工程とを備え、
 前記マイクロカプセル塗布工程は、前記マイクロカプセルが静電塗布により前記原紙に塗布されることを特徴とすることを特徴とする。
Invention of Claim 4 in the manufacturing method of a sanitary thin paper,
A microcapsule application process for applying microcapsules to a sanitary thin paper base;
A liquid application process for applying a lotion chemical to a sanitary thin paper base,
The microcapsule application step is characterized in that the microcapsules are applied to the base paper by electrostatic application.
 請求項5に記載の発明は、請求項4記載の衛生薄葉紙の製造方法において、
 前記液体塗布工程は、ローターダンプニング印刷方式により行われることを特徴とする。
 請求項6に記載の発明は、請求項4又は5記載に記載の衛生薄葉紙の製造方法において、
 前記マイクロカプセル塗布工程は、ウレタン、尿素-メラミン、尿素-ホルマリンのいずれかを主たる原料とする前記マイクロカプセルの塗布が行われることを特徴とする。
Invention of Claim 5 is a manufacturing method of the sanitary thin paper of Claim 4,
The liquid application process is performed by a rotor dampening printing method.
Invention of Claim 6 is a manufacturing method of the sanitary thin paper of Claim 4 or 5,
The microcapsule coating step is characterized in that the microcapsule is mainly coated with any one of urethane, urea-melamine, and urea-formalin.
 本発明にかかる衛生薄葉紙の製造装置又は製造方法によれば、ローション薬液にマイクロカプセルを混入させる必要がないので、マイクロカプセルの機能性について調整する場合でも塗布するマイクロカプセルのみを交換すれば良く、ローション薬液の交換を伴わないので、作業負担の軽減と作業時間の低減を図ることができ、衛生薄葉紙の生産性を向上させることが可能となる。 According to the sanitary thin paper manufacturing apparatus or manufacturing method of the present invention, since it is not necessary to mix microcapsules into the lotion chemical solution, only the microcapsules to be applied need to be replaced even when adjusting the functionality of the microcapsules. Since the lotion chemical solution is not exchanged, the work load can be reduced and the work time can be reduced, and the productivity of sanitary thin paper can be improved.
本発明の実施形態である衛生薄葉紙の製造装置の概略構成図である。It is a schematic block diagram of the manufacturing apparatus of the sanitary thin paper which is embodiment of this invention. 図1の製造装置のマイクロカプセル塗布装置の詳細を示す構成図である。It is a block diagram which shows the detail of the microcapsule application | coating apparatus of the manufacturing apparatus of FIG. 衛生薄葉紙の製造方法における用紙供給工程を示す説明図である。It is explanatory drawing which shows the paper supply process in the manufacturing method of a sanitary thin paper. マイクロカプセル塗布工程を示す説明図である。It is explanatory drawing which shows a microcapsule application | coating process. 液体塗布工程を示す説明図である。It is explanatory drawing which shows a liquid application process. 実施例と比較例による操業性及び官能評価の比較試験の条件及び結果を示す図表である。It is a table | surface which shows the conditions and result of the comparative test of operativity and sensory evaluation by an Example and a comparative example.
[発明の実施の形態の概略]
 本発明の実施の形態について図面に基づいて説明する。
 図1は本発明の実施の形態である衛生薄葉紙の製造装置の概略構成図である。
 この衛生薄葉紙の製造装置10は、衛生薄葉紙の原紙に対してローション薬液とマイクロカプセルとを塗布することを主たる目的とする製造装置である。
[Outline of Embodiment of the Invention]
Embodiments of the present invention will be described with reference to the drawings.
FIG. 1 is a schematic configuration diagram of a sanitary thin paper manufacturing apparatus according to an embodiment of the present invention.
This sanitary thin paper manufacturing apparatus 10 is a manufacturing apparatus whose main purpose is to apply lotion chemicals and microcapsules to a base paper of sanitary thin paper.
[衛生薄葉紙の原紙]
 本発明の衛生薄葉紙の原紙としては、JIS P 8124(1998)による坪量が10~18g/m2であるクレープ紙を積層して2プライとしたものであるのが望ましい。また、JIS P 8111(1998)の条件下で、ダイヤルシックネスゲージ(厚み測定器)「PEACOCK G型」(尾崎製作所製)を用いて2プライのままで測定した紙厚は80~250μm、好ましくは100~200μm、より好ましくは130~180μmとするのが望ましい。JIS P 8113(1998)に規定される乾燥引張強度(以下、乾燥紙力ともいう)の縦方向が、2プライで200~700cN/25mm、好ましくは250~600cN/25mm、特に好ましくは300~600cN/25mmとされ、他方、横方向が、2プライで50~250cN/25mm、好ましくは80~220cN/25mm、特に好ましくは100~200cN/25mmとされる。乾燥引張強度が低すぎると、製造時及び使用時の断紙や伸び等のトラブルが発生し易くなり、高過ぎると使用時にごわごわした肌触りとなる。なお、本発明における衛生薄葉紙としては、ティッシュペーパー、トイレットペーパー、ペーパタオルなどが挙げられる。
[Base paper for sanitary thin paper]
The base paper of the sanitary thin paper of the present invention is preferably a two-ply laminate of crepe paper having a basis weight of 10 to 18 g / m 2 according to JIS P 8124 (1998). Further, the paper thickness measured with a dial thickness gauge (thickness measuring instrument) “PEACOCK G type” (manufactured by Ozaki Mfg. Co., Ltd.) under the conditions of JIS P 8111 (1998) is 80 to 250 μm, preferably It is desirable that the thickness is 100 to 200 μm, more preferably 130 to 180 μm. The longitudinal direction of dry tensile strength (hereinafter also referred to as dry paper strength) specified in JIS P 8113 (1998) is 200 to 700 cN / 25 mm, preferably 250 to 600 cN / 25 mm, particularly preferably 300 to 600 cN with 2 plies. On the other hand, the lateral direction is 50 to 250 cN / 25 mm, preferably 80 to 220 cN / 25 mm, particularly preferably 100 to 200 cN / 25 mm with 2 plies. If the dry tensile strength is too low, troubles such as paper breakage and elongation at the time of production and use are likely to occur, and if it is too high, the touch becomes stiff during use. In addition, as a sanitary thin paper in this invention, tissue paper, toilet paper, paper towel, etc. are mentioned.
 また、本発明に係る原紙は、その原料は公知のものが使用できるが、特に、パルプ原料は、NBKPとLBKPとで構成されているのが好ましい。適宜古紙パルプが配合されていてもよいが、水系のローション薬液との相性がよく、得られる風合いの点でも望ましいことから、バージンパルプのNBKPとLBKPのみから構成されているのがよい。その場合の配合割合(JIS P 8120)としては、NBKP:LBKP=10:90~70:30がよく、特に、NBKP:LBKP=30:70~60:40が望ましい。 In addition, as the raw paper according to the present invention, known raw materials can be used. In particular, the pulp raw material is preferably composed of NBKP and LBKP. Waste paper pulp may be blended as appropriate, but it is preferably composed only of NBKP and LBKP of virgin pulp because it is compatible with an aqueous lotion solution and desirable in terms of the resulting texture. In this case, the mixing ratio (JIS (P 8120) is preferably NBKP: LBKP = 10: 90 to 70:30, and particularly preferably NBKP: LBKP = 30: 70 to 60:40.
[衛生薄葉紙に塗布するローション薬液]
 本発明では、衛生薄葉紙の原紙中にローション薬液が塗布される。ローション薬液の塗布は、2プライに積層された原紙の両面に対して行なうのが望ましい。そして、本発明におけるローション薬液の塗布量は、原紙重量(米坪)の20~30重量%の範囲とすることが望ましい。
 ローション薬液としては、水及びポリオールを含有するものとする。特には、ポリオールを70~90%、水分を10~20%を含むもの、特に好ましくは、さらに機能性薬剤を0.01~22%含むものである。かかる水系薬液は、原紙のクレープを伸ばす作用があり、保湿性とともに衛生薄葉紙の表面の滑らかさをも向上させる。
[Lotion solution applied to sanitary thin paper]
In the present invention, the lotion chemical is applied to the base paper of the sanitary thin paper. The lotion solution is preferably applied to both sides of the base paper laminated on the two plies. The application amount of the lotion chemical in the present invention is preferably in the range of 20 to 30% by weight of the base paper weight (US tsubo).
The lotion chemical solution contains water and a polyol. In particular, those containing 70 to 90% polyol and 10 to 20% water, particularly preferably 0.01 to 22% further containing a functional drug. Such an aqueous chemical solution has an action of extending the crepe of the base paper, and improves the smoothness of the surface of the sanitary thin paper as well as the moisture retention.
 なお、ポリオールはグリセリン、ジグリセリン、プロピレングリコール、1,3-ブチレングリコール、ポリエチレングリコール、およびその誘導体等の多価アルコール、ソルビトール、グルコース、キシリトール、マルトース、マルチトール、マンニトール、トレハロース等の糖類を含む。 The polyol includes polyhydric alcohols such as glycerin, diglycerin, propylene glycol, 1,3-butylene glycol, polyethylene glycol, and derivatives thereof, and saccharides such as sorbitol, glucose, xylitol, maltose, maltitol, mannitol, and trehalose. .
 機能性薬剤としては、柔軟剤、界面活性剤、無機および有機の微粒子粉体、油性成分などがある。柔軟剤、界面活性剤は衛生薄葉紙に柔軟性を与えたり表面を滑らかにしたりする効果があり、アニオン性界面活性剤、カチオン性界面活性剤及び両性イオン界面活性剤を適用する。無機および有機の微粒子粉体は表面を滑らかな肌触りとする。油性成分は滑性を高める働きがあり、流動パラフィン、セタノール、ステアリルアルコール、オレイルアルコール等の高級アルコールを用いることができる。 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 sanitary thin paper 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.
 また機能性薬剤としてポリオールの保湿性を維持させる薬剤として親水性高分子ゲル化剤、コラーゲン、加水分解コラーゲン、加水分解ケラチン、加水分解シルク、ヒアルロン酸若しくはその塩、セラミド等の1種以上を任意の組合せ等の保湿剤を加えることができる。
 また機能性薬剤として香料、各種天然エキス等のエモリエント剤、ビタミン類、配合成分を安定させる乳化剤、ローション薬液の発泡を抑え塗布を安定させるための消泡剤、防黴剤、有機酸などを適宜配合することができる。さらには、ビタミンC、ビタミンEの抗酸化剤を含有させてもよい。
 上記成分のうち、グリセリン、プロピレングリコール等の多価アルコールを主成分とする場合には、ローション薬液の粘度、塗布量を安定させる点で、塗布の点で好ましい。
In addition, as a functional agent, one or more of a hydrophilic polymer gelling agent, collagen, hydrolyzed collagen, hydrolyzed keratin, hydrolyzed silk, hyaluronic acid or a salt thereof, ceramide, etc. are optionally selected as agents that maintain the moisture retention of polyol. A moisturizer such as a combination of the above can be added.
In addition, emollients such as fragrances and various natural extracts, vitamins, emulsifiers that stabilize compounding ingredients, antifoaming agents, antifungal agents, organic acids, etc., that suppress foaming of lotion chemicals and stabilize application as functional agents. Can be blended. Furthermore, you may contain the antioxidant of vitamin C and vitamin E.
Among the above components, when the main component is a polyhydric alcohol such as glycerin or propylene glycol, it is preferable from the viewpoint of application in terms of stabilizing the viscosity and application amount of the lotion chemical.
[衛生薄葉紙に塗布するマイクロカプセル]
 一方、本発明では、マイクロカプセルがローション薬液とは別に原紙に塗布される。
 本発明のマイクロカプセルとしては、後述する衛生薄葉紙の製造装置10のマイクロカプセル塗布装置40による静電塗布に適したものであることが望ましい。
[Microcapsules applied to sanitary thin paper]
On the other hand, in this invention, a microcapsule is apply | coated to a base paper separately from a lotion chemical | medical solution.
The microcapsules of the present invention are preferably suitable for electrostatic coating by the microcapsule coating apparatus 40 of the sanitary thin paper manufacturing apparatus 10 described later.
 マイクロカプセルは香料を内包している。かかるマイクロカプセルの材料としては、ウレタン、尿素-メラミン、尿素-ホルマリン、寒天、ゼラチンを主原料とするものが利用可能だが、当該マイクロカプセルは、ローション薬液に曝されるので、水分に対する安定性からウレタン、尿素-メラミン、尿素-ホルマリンがより好ましい。
 なお、マイクロカプセルは、後述する製造装置10のマイクロカプセル塗布装置40においてドクターブレード44による掻き取りが行われるので、当該掻き取りに耐え得る強度に設計することが望ましい。マイクロカプセルの膜厚は、特に限定されないが、概ね、0.1~1.0μm、好ましくは0.1~0.5μmである。香料含有マイクロカプセル32mの平均粒子径は、10~50μmであるのが望ましい。この範囲であれば、カプセル重量に対する香料比を大きくすることができ所望の芳香シート材に十分な香料量を含有させることができる。但し、カプセル径が大きくなると製造時にカプセルが多量に破壊されて歩留まりの低下するおそれがあるため、より好ましい香料含有マイクロカプセルの平均粒径は、15~30μmである。なお、ここでの平均粒子径は、メジアン径による。
Microcapsules contain perfume. As materials for such microcapsules, those mainly composed of urethane, urea-melamine, urea-formalin, agar, and gelatin can be used. However, since the microcapsules are exposed to lotion chemicals, Urethane, urea-melamine, and urea-formalin are more preferable.
In addition, since the microcapsule is scraped off by the doctor blade 44 in the microcapsule coating apparatus 40 of the manufacturing apparatus 10 to be described later, it is desirable to design the microcapsule so as to withstand the scraping. The film thickness of the microcapsule is not particularly limited, but is generally 0.1 to 1.0 μm, preferably 0.1 to 0.5 μm. The average particle size of the perfume-containing microcapsules 32 m is preferably 10 to 50 μm. If it is this range, the fragrance | flavor ratio with respect to a capsule weight can be enlarged, and sufficient fragrance | flavor amount can be contained in a desired fragrance sheet material. However, when the capsule diameter is increased, a large amount of capsules may be destroyed at the time of production and the yield may be lowered. Therefore, a more preferable average particle diameter of the perfume-containing microcapsules is 15 to 30 μm. Here, the average particle diameter depends on the median diameter.
 また、マイクロカプセルに内包させる香料として、冷涼剤及びl-メントールを含むメントール系香料を用いる。この香料は、鼻をかんだ際に、メントールの揮発性及び冷涼剤により、皮膚に優れた冷涼感を与える。 Also, a menthol-based fragrance containing a cooling agent and l-menthol is used as a fragrance included in the microcapsule. This fragrance gives the skin an excellent cooling feeling due to the volatility and cooling agent of menthol when biting the nose.
[衛生薄葉紙の製造装置:全体構成]
 衛生薄葉紙の製造装置10は、図1に示すように、原紙Pのロールを保持して原紙の繰り出しを行う原紙供給装置20と、原紙Pに対してマイクロカプセルを塗布するマイクロカプセル塗布装置40と、原紙Pに対してローション薬液を塗布する液体塗布装置30と、原紙Pを折り畳みながら積み重ねる積層装置60とを備えている。
[Sanitary thin paper manufacturing equipment: overall configuration]
As shown in FIG. 1, the sanitary thin paper manufacturing apparatus 10 includes a base paper supply device 20 that holds a roll of base paper P and feeds the base paper, and a microcapsule application device 40 that applies microcapsules to the base paper P. The liquid application device 30 for applying the lotion chemical solution to the base paper P and the laminating device 60 for stacking the base paper P while being folded are provided.
[原紙供給装置]
 衛生薄葉紙の原紙Pは、製造装置10の前段階として、先ず、抄紙装置においてパルプ繊維(望ましくは古紙パルプを含まないバージンパルプ100%のパルプ繊維)から薄葉紙を抄造し、必要によりクレープを施し、カレンダー処理を施した上で、これを巻き取り、一次原反ロール(一般にジャンボロールともいわれている)を製造し、次いで図示しないが、この一次原反ロールを公知のプライマシンにセットし、複数の一次原反ロールから繰り出した一次連続シートを重ね合わせて巻き取るとともに輪切り(幅方向に複数に分割)にし、複数枚のプライからなる二次原反ロールを製造する。
[Base paper feeder]
The base paper P of sanitary thin paper, as a pre-stage of the production apparatus 10, first, a thin paper is made from pulp fibers (preferably 100% virgin pulp fiber not containing waste paper pulp) in a paper making apparatus, and crepe is applied if necessary. After the calendar treatment, this is wound up to produce a primary raw roll (generally also referred to as a jumbo roll). Then, although not shown, this primary raw roll is set in a known ply machine, The primary continuous sheet fed from the primary raw roll is superposed and wound, and is cut into a plurality of pieces (divided into a plurality of parts in the width direction) to produce a secondary raw roll made of a plurality of plies.
 原紙供給装置20は、プライマシンで製造された二つの二次原反ロール21を回転可能に保持し、それぞれの二次原反ロールから二次連続シートを原紙Pとして繰り出しを行う。
 かかる原紙供給装置20は、各二次原反ロール21から繰り出される原紙Pを個別に搬送する搬送ローラ22と、各搬送ローラ22により形成されるそれぞれの搬送経路の途中に設けられたテンションローラ23とを備えている。
 上記テンションローラ23は、搬送ローラ22により搬送される原紙Pに加えられる張力を制御するためのものである。
The base paper supply device 20 rotatably holds two secondary raw rolls 21 manufactured by a ply machine, and feeds a secondary continuous sheet from each secondary raw roll as base paper P.
The base paper supply device 20 includes a transport roller 22 that individually transports the base paper P fed from each secondary raw roll 21, and a tension roller 23 provided in the middle of each transport path formed by each transport roller 22. And.
The tension roller 23 is for controlling the tension applied to the base paper P transported by the transport roller 22.
[マイクロカプセル塗布装置]
 マイクロカプセル塗布装置40は、マイクロカプセルをローション薬液に混入させることなく原紙Pに塗布するものであって、2ルートで搬送されるそれぞれの原紙Pについて、片面にマイクロカプセルの塗布を行う二基の塗布ユニット41を備えている。
 各塗布ユニット41は、図2に示すように、マイクロカプセルが充填されたマイクロカプセル貯留部42と、マイクロカプセル貯留部42の下部に配置されて充填されたマイクロカプセルに外周面の上部が曝された散布ローラ43と、散布ローラ43の外周面に摺接して付着したマイクロカプセルを均一な膜状とするドクターブレード44と、散布ローラ43に対して原紙Pの搬送方向上流側と下流側とに接する二つの飛散防止ローラ45と、散布ローラ43と二つの飛散防止ローラ45のそれぞれの外周に摺接する放電線46と、搬送される原紙Pの下側に配置された帯電器47とを備えている。
[Microcapsule coating device]
The microcapsule coating apparatus 40 applies microcapsules to the base paper P without mixing it into the lotion chemical solution, and applies two microcapsules to one side of each base paper P transported by two routes. A coating unit 41 is provided.
As shown in FIG. 2, each coating unit 41 has a microcapsule reservoir 42 filled with microcapsules and an upper portion of the outer peripheral surface exposed to the microcapsules arranged and filled below the microcapsule reservoir 42. The spray roller 43, the doctor blade 44 having a uniform film-like microcapsule attached in sliding contact with the outer peripheral surface of the spray roller 43, and the upstream side and the downstream side in the transport direction of the base paper P with respect to the spray roller 43 Two scattering prevention rollers 45 that are in contact with each other, a discharge line 46 that is in sliding contact with the outer periphery of each of the spraying roller 43 and the two scattering prevention rollers 45, and a charger 47 that is disposed below the base paper P being conveyed. Yes.
 マイクロカプセル貯留部42はその下部が広く開口し、当該開口部を塞ぐように散布ローラ43が配置されている。これにより、散布ローラ43の外周面の上部がマイクロカプセル貯留部42の内部に充填されたマイクロカプセルに曝された状態となり、当該散布ローラ43が回転を行うことによってその外周面の周全体にマイクロカプセルが付着する。
 ドクターブレード44は、散布ローラ43に対して原紙Pの搬送方向の上流側と下流側とにそれぞれ設けられており、回転を行う散布ローラ43の外周面に付着したマイクロカプセルを均一な厚さに薄層化する。
The lower part of the microcapsule storage part 42 is widely opened, and the spraying roller 43 is arranged so as to close the opening part. As a result, the upper part of the outer peripheral surface of the spraying roller 43 is exposed to the microcapsules filled in the microcapsule storage part 42, and the spraying roller 43 rotates so that the entire circumference of the outer peripheral surface is microscopic. The capsule adheres.
The doctor blade 44 is provided on the upstream side and the downstream side in the conveying direction of the base paper P with respect to the spreading roller 43, respectively, and the microcapsules attached to the outer peripheral surface of the spreading roller 43 that rotates are made to have a uniform thickness. Thin layer.
 二つの飛散防止ローラ45は、散布ローラ43に摺接して回転を行う。散布ローラ43の下側は、当該散布ローラ43と二つの飛散防止ローラ45とに囲まれたマイクロカプセル散布領域が形成されている。
 そして、二つの飛散防止ローラ45の外周の下部に対して僅かな隙間をあけた状態で原紙Pが搬送される。この時、マイクロカプセル散布領域内で散布ローラ43と二つの飛散防止ローラ45にそれぞれ摺接する放電線46が除伝を行うことにより、マイクロカプセルが散布ローラ43及び二つの飛散防止ローラ45の外周面から掻き落とされ、原紙P側に落下する。
 また、原紙Pの下側に配置された帯電器47が帯電状態となることにより、マイクロカプセル散布領域内のマイクロカプセルを原紙P側に引き寄せるので、原紙Pに対してより効果的にマイクロカプセルの塗布を行うことができる。
The two anti-scattering rollers 45 rotate in sliding contact with the spraying roller 43. A microcapsule spraying region surrounded by the spraying roller 43 and the two scattering prevention rollers 45 is formed below the spraying roller 43.
And the base paper P is conveyed in the state which left a little clearance gap with respect to the lower part of the outer periphery of the two scattering prevention rollers 45. At this time, the discharge line 46 slidably contacting the spraying roller 43 and the two scattering prevention rollers 45 in the microcapsule spraying area removes power, so that the microcapsules are outer peripheral surfaces of the spreading roller 43 and the two scattering prevention rollers 45. Is scraped off and falls to the base paper P side.
In addition, since the charger 47 disposed on the lower side of the base paper P is in a charged state, the microcapsules in the microcapsule spraying area are attracted to the base paper P side. Application can be performed.
[液体塗布装置]
 液体塗布装置30は、2ルートで搬送されるそれぞれの原紙Pについて、表面にローション薬液の塗布を行うものと裏面にローション薬液の塗布を行うものとで合計四基の塗布ユニット31を備えている。
 塗布ユニット31は、ローターダンプニング印刷方式のローターダンプニング印刷装置としての構成を採っており、ローション薬液を噴霧する噴霧器32と、当該噴霧器32の前方に対向配置され、その外周面に原紙Pを沿わせて搬送するバックローラ33とを備え、バックローラ33によって搬送される原紙Pに対して噴霧器32によりローション薬液の塗布が行われる。
 これらの構成により、2ルートで搬送されるそれぞれの原紙Pの両面にローション薬液が塗布される。
[Liquid coating device]
The liquid coating apparatus 30 includes a total of four coating units 31 for each base paper P transported in two routes, one for applying lotion chemical on the front side and one for applying lotion chemical on the back side. .
The coating unit 31 has a configuration as a rotor dampening printing type rotor dampening printing device, and is disposed opposite to a sprayer 32 for spraying a lotion chemical solution, in front of the sprayer 32, and a base paper P is placed on the outer peripheral surface thereof. A back roller 33 that is conveyed along the back roller 33 is applied, and a lotion chemical is applied to the base paper P conveyed by the back roller 33 by the sprayer 32.
With these configurations, the lotion solution is applied to both surfaces of each base paper P conveyed by the two routes.
[積層装置]
 積層装置60は、2ルートで搬送されるそれぞれの原紙Pに個別にエンボス加工を行う二つのエンボスローラ61と、それぞれの原紙Pを折り畳みながら積み重ねる積層部62とを備えている。これらは周知のものと同一であるため詳細な説明は省略する。
[Lamination equipment]
The laminating apparatus 60 includes two embossing rollers 61 that individually emboss each base paper P conveyed by two routes, and a stacking unit 62 that stacks the base papers P while being folded. Since these are the same as well-known ones, detailed description thereof is omitted.
[衛生薄葉紙の製造方法]
 図3は衛生薄葉紙の製造工程を順番に示した説明図である。製造装置10を用いた衛生薄葉紙の製造方法を図1~図3に基づいて説明する。
 まず、パルプ繊維から抄造された2プライの薄葉紙からなる原紙Pが巻かれた二つの二次原反ロール21が用意され、原紙供給装置20にセットされる。そして、原紙Pが2ルートで下流側に供給される。この時、それぞれの原紙Pは、テンションローラ23により所定の張力が付与された状態でマイクロカプセル塗布装置40に送られる(図3A:用紙供給工程)。
[Manufacturing method of sanitary thin paper]
FIG. 3 is an explanatory view showing the manufacturing process of sanitary thin paper in order. A method for manufacturing sanitary thin paper using the manufacturing apparatus 10 will be described with reference to FIGS.
First, two secondary web rolls 21 on which a base paper P made of 2-ply thin paper made from pulp fibers is wound are prepared and set in the base paper supply device 20. Then, the base paper P is supplied downstream by two routes. At this time, each base paper P is sent to the microcapsule coating apparatus 40 in a state where a predetermined tension is applied by the tension roller 23 (FIG. 3A: paper supply process).
 次いで、各原紙Pはマイクロカプセル塗布装置40において、片面について個々の塗布ユニット41によりマイクロカプセルの塗布が行われる。マイクロカプセル塗布装置40は静電塗布を行うので、静電気力によりマイクロカプセルは原紙Pの平面に付着する(図3B:マイクロカプセル塗布工程)。なお、図3B中の符号mはマイクロカプセルを示す。 Next, each base paper P is coated with a microcapsule on one side by an individual coating unit 41 in a microcapsule coating apparatus 40. Since the microcapsule coating apparatus 40 performs electrostatic coating, the microcapsules adhere to the plane of the base paper P by electrostatic force (FIG. 3B: microcapsule coating process). In addition, the code | symbol m in FIG. 3B shows a microcapsule.
 次いで、各原紙Pは液体塗布装置30において、搬送される原紙Pの両側に配置されたそれぞれの塗布ユニット31によって、その両面にローション薬液が塗布される(図3C:液体塗布工程)。塗布されたローション薬液は原紙Pの内側に浸透する。なお、図3C中の符号lはローション薬液を示す。 Next, each base paper P is applied with a lotion solution on both sides thereof by the respective application units 31 arranged on both sides of the transported base paper P in the liquid application device 30 (FIG. 3C: liquid application step). The applied lotion solution penetrates inside the base paper P. In addition, the code | symbol 1 in FIG. 3C shows a lotion chemical | medical solution.
 次いで、各原紙Pは積層装置60において、各エンボスローラ61によりエンボスが付与され、さらに、積層部62により折り畳まれて積み重ねられる(積層工程)。
 このようにして折り畳まれ、積層された原紙Pは、最終的には、後段設備において製品幅と同幅の間隔をおいて裁断され、箱詰め、包装等の処理を経て製品(衛生薄葉紙)となる。
Next, each base paper P is embossed by each embossing roller 61 in the laminating apparatus 60, and further folded and stacked by the laminating unit 62 (lamination process).
The base paper P folded and laminated in this manner is finally cut at an interval of the same width as the product width in the subsequent equipment, and becomes a product (sanitary thin paper) through processing such as boxing and packaging. .
[発明の実施の形態の技術的効果]
 上記衛生薄葉紙の製造装置10は、液体塗布装置30とは別の工程で原紙Pにマイクロカプセルを塗布するマイクロカプセル塗布装置40と、原紙Pにローション薬液を塗布する液体塗布装置30とを備えているので、マイクロカプセル塗布工程と液体塗布工程とがそれぞれ別工程で行われることとなる。
 このため、ローション薬液にマイクロカプセルを混入させて塗布する場合と異なり、マイクロカプセルの機能性の調整、例えば、香料の強度や種別を変更する場合でも塗布するマイクロカプセルのみを交換すれば良く、ローション薬液の交換を伴わないので、作業負担の軽減と作業時間の低減を図ることができ、衛生薄葉紙の生産性を向上させることが可能となる。
 また、上記構成の製造装置10は、従来からあるローション薬液を塗布し、マイクロカプセルを塗布しない衛生薄葉紙の製造装置に対してマイクロカプセル塗布装置40を加えるだけ実現することができ、既存の設備利用を図ることができる。
[Technical effects of the embodiment of the invention]
The sanitary thin paper manufacturing apparatus 10 includes a microcapsule applicator 40 that applies microcapsules to the base paper P in a separate process from the liquid applicator 30, and a liquid applicator 30 that applies a lotion chemical to the base paper P. Therefore, the microcapsule application process and the liquid application process are performed in separate processes.
For this reason, unlike the case where microcapsules are mixed and applied in a lotion chemical solution, adjustment of the functionality of the microcapsules, for example, even when changing the intensity or type of fragrance, only the microcapsules to be applied need to be replaced. Since the chemical solution is not exchanged, it is possible to reduce the work load and the work time, and it is possible to improve the productivity of sanitary thin paper.
In addition, the manufacturing apparatus 10 having the above-described configuration can be realized only by adding the microcapsule coating apparatus 40 to a conventional sanitary thin sheet manufacturing apparatus that applies a lotion chemical solution and does not apply microcapsules. Can be achieved.
 また、製造装置10のマイクロカプセル塗布装置40は、その塗布ユニット41が放電線46と帯電器47とを備え、マイクロカプセルを静電塗布により原紙Pに塗布するので、マイクロカプセル塗布工程を静電塗布により行うことができる。
 これにより、マイクロカプセルのローション薬液への混入を不要としつつも、マイクロカプセル塗布の際にマイクロカプセルが粉塵化して周囲に拡散することを効果的に抑制することが可能となる。
The microcapsule coating apparatus 40 of the manufacturing apparatus 10 includes the discharge unit 46 and the charger 47, and the microcapsule is applied to the base paper P by electrostatic coating. It can be performed by coating.
This makes it possible to effectively prevent the microcapsules from becoming dust and diffusing around when applying the microcapsules, while making it unnecessary to mix the microcapsules into the lotion chemical.
 また、製造装置10の液体塗布装置30は、ローターダンプニング印刷装置であることから、液体塗布工程においてローターダンプニング印刷方式によりローション薬液の塗布を行うことができる。
 これにより、グラビア印刷やフレキソ印刷のように、ローション薬液を原紙に供給するための溝や凸条が形成された特殊形状のローラを使用することなく、簡易な構成により塗布を行うことが可能となる。
Moreover, since the liquid application apparatus 30 of the manufacturing apparatus 10 is a rotor dampening printing apparatus, the lotion chemical can be applied by a rotor dampening printing method in the liquid application process.
This makes it possible to apply with a simple configuration without using a specially shaped roller with grooves and ridges for supplying lotion chemicals to the base paper, such as gravure printing and flexographic printing. Become.
 また、製造装置10では、マイクロカプセル塗布工程において塗布するマイクロカプセルとして、ウレタン、尿素-メラミン、尿素-ホルマリンのいずれかを主たる原料とするものを利用している。
 これらを主材料とするマイクロカプセルであればローション薬液に曝されても安定性を維持することができ、衛生薄葉紙を使用するまで香料を保持することが可能である。また、衛生薄葉紙が香料の機能を失わない耐用期限を長く維持することが可能となる。
Further, in the manufacturing apparatus 10, a microcapsule to be applied in the microcapsule application step uses a material mainly made of urethane, urea-melamine, or urea-formalin.
If it is a microcapsule which uses these as a main material, even if it exposes to a lotion chemical | medical solution, stability can be maintained and it is possible to hold | maintain a fragrance | flavor until it uses sanitary thin paper. Moreover, it becomes possible to maintain a long service life in which the sanitary thin paper does not lose the function of the fragrance.
[その他]
 なお、上記製造装置10の液体塗布装置30による液体塗布工程は、ローターダンプニング方式に限定されない。例えば、フレキソ印刷方式、ロール転写方式、インクジェット方式、スプレー方式、グラビア印刷方式等の他の液体塗布方法を利用しても良い。
[Others]
In addition, the liquid application process by the liquid application apparatus 30 of the manufacturing apparatus 10 is not limited to the rotor dampening method. For example, other liquid application methods such as a flexographic printing method, a roll transfer method, an ink jet method, a spray method, and a gravure printing method may be used.
 また、マイクロカプセル塗布装置40によりマイクロカプセル塗布工程は、静電塗布に限定されない。例えば、静電吹き付け方式、スプレー方式等の他の粉体塗布方法をマイクロカプセルの塗布に適用しても良い。
 また、静電力を利用しない方式を採用する場合には、マイクロカプセルは、静電塗布に適したものに限らず、より広範囲の種類の材料からなるマイクロカプセルを使用することが可能である。
Further, the microcapsule coating process by the microcapsule coating apparatus 40 is not limited to electrostatic coating. For example, other powder coating methods such as electrostatic spraying and spraying may be applied to the microcapsules.
When a method that does not use electrostatic force is adopted, the microcapsules are not limited to those suitable for electrostatic coating, and microcapsules made of a wider range of materials can be used.
 また、香料を内包するマイクロカプセルを利用する場合を例示したが、他の機能成分を内包するマイクロカプセルを利用しても良い。 Moreover, although the case where the microcapsule which encloses a fragrance | flavor was utilized was illustrated, the microcapsule which encloses another functional component may be utilized.
 (実施例1、2および比較例1~3)
 図4の図表に示す各種の2プライティッシュペーパー(実施例1、2および比較例1~3)を製造し、表中に記したローション薬液及び香料カプセルを塗布し、操業性及び官能評価を行った。なお、ローション薬液は5.6g/m、香料カプセル(マイクロカプセル)は平均粒子径が10μmのものを0.60g/mを塗布した。
 実施例1は、香料カプセル粉体(マイクロカプセル)を静電装置により塗布した後、ローション薬液をグラビア方式で塗布した。実施例2は、香料カプセル粉体(マイクロカプセル)を静電装置により塗布した後、ローション薬液をスプレー方式で塗布した。
 比較例1は、ローション薬液中に香料カプセル(マイクロカプセル)を混合した薬液をグラビア塗工した。その際、静電装置は使用していない。
 比較例2は、ローション薬液をグラビア方式で塗布した後、香料カプセル(マイクロカプセル)を水に分散させてスプレー塗布した。その際、静電装置は使用していない。
 比較例3は、ローション薬液をグラビア方式で塗布した後、香料カプセル(マイクロカプセル)を水に分散させてグラビア塗工した。その際、静電装置は使用していない。
(Examples 1 and 2 and Comparative Examples 1 to 3)
Various two-ply tissue papers (Examples 1 and 2 and Comparative Examples 1 to 3) shown in the chart of FIG. 4 were produced, and the lotion solution and the fragrance capsule described in the table were applied, and the operability and sensory evaluation were performed. It was. The lotion chemical solution was applied at 5.6 g / m 2 , and the fragrance capsule (microcapsule) having an average particle diameter of 10 μm was applied at 0.60 g / m 2 .
In Example 1, a fragrance capsule powder (microcapsule) was applied by an electrostatic device, and then a lotion chemical was applied by a gravure method. In Example 2, a fragrance capsule powder (microcapsule) was applied by an electrostatic device, and then a lotion chemical was applied by a spray method.
In Comparative Example 1, a chemical solution in which a fragrance capsule (microcapsule) was mixed in a lotion chemical solution was subjected to gravure coating. At that time, no electrostatic device is used.
In Comparative Example 2, a lotion chemical was applied by a gravure method, and then a fragrance capsule (microcapsule) was dispersed in water and sprayed. At that time, no electrostatic device is used.
In Comparative Example 3, a lotion chemical solution was applied by a gravure method, and then a perfume capsule (microcapsule) was dispersed in water for gravure coating. At that time, no electrostatic device is used.
 (柔らかさの官能評価)
 柔らかさの官能評価については、被験者10名により、紙の表面を手で触った際の柔らかさについて5点満点(5点:とても良い、4点:良い、3点:どちらでもない、2点:悪い、1点:とても悪い)で点数をつけて平均点を算出し、その平均点が、4点以上の場合を「◎」、3点以上4点未満の場合を「〇」、3点未満を「×」とそれぞれ評価した。
(Sensory evaluation of softness)
For sensory evaluation of softness, 10 subjects gave a 10-point score for the softness when touching the surface of the paper with their hands (5 points: very good, 4 points: good, 3 points: none of them, 2 points : Bad, 1 point: very bad), and the average score is calculated. If the average score is 4 points or more, “◎”, if 3 points or more and less than 4 points, “◯”, 3 points Less than “x” was evaluated.
 (香りの強さの官能評価)
 香りの強さの官能評価については、被験者10名により、紙の表面を鼻にあてた際の香りの強さについて5点満点(5点:とても良い、4点:良い、3点:どちらでもない、2点:悪い、1点:とても悪い)で点数をつけて平均点を算出し、その平均点が、4点以上の場合を「◎」、3点以上4点未満の場合を「〇」、3点未満を「×」とそれぞれ評価した。
(Sensory evaluation of scent strength)
For sensory evaluation of scent intensity, 10 subjects gave a maximum score of 5 (5 points: very good, 4 points: good, 3 points: either) No, 2 points: bad, 1 point: very bad), and an average score is calculated. If the average score is 4 points or more, “◎”, if it is 3 points or more and less than 4 points, “○ The less than 3 points were evaluated as “x”.
 (薬液切り替え時間)
 薬液の切り替え時間は、ローション薬液を0.8mのタンクから0.5mの薬液を抜き取り、系内の紛体を水で洗い流した上でタンク内に薬液を0.5m入れた際の所要時間が0.5時間未満の場合を「◎」、0.5時間以上1.0時間未満の場合を「〇」、1.0時間以上の場合を「×」とした。
(Chemical solution switching time)
Switching time of the chemical solution, the required lotion chemical from tank 0.8 m 3 withdrawn chemical 0.5 m 3, when the powder in the system the chemical was placed 0.5 m 3 in the tank after having washed away with water The case where the time was less than 0.5 hours was “◎”, the case where the time was 0.5 hours or more and less than 1.0 hour was “◯”, and the case where the time was 1.0 hours or more was “x”.
 (設備の残香)
 残香がない場合を「◎」、残香がある場合を「×」とした。
(Remaining scent of equipment)
The case where there was no remaining scent was designated as “◎”, and the case where there was a remaining scent was designated as “x”.
 表1からもわかる通り、本発明に係る実施例1、実施例2は、比較例1~3とは異なり、優れた柔らかさと香りの強さを示し、なおかつ設備の残香がないため、薬液の切り替え時間が短縮された。 As can be seen from Table 1, Example 1 and Example 2 according to the present invention differ from Comparative Examples 1 to 3 in that they exhibit excellent softness and fragrance strength, and there is no residual scent of equipment. Switching time has been shortened.
 本発明は、薄葉紙の製造分野において好適に利用できる。 The present invention can be suitably used in the field of manufacturing thin paper.
10 製造装置
20 原紙供給装置
21 二次原反ロール
22 搬送ローラ
23 テンションローラ
30 液体塗布装置
31 塗布ユニット
32 噴霧器
33 バックローラ
40 マイクロカプセル塗布装置
41 塗布ユニット
42 マイクロカプセル貯留部
43 散布ローラ
44 ドクターブレード
45 飛散防止ローラ
46 放電線
47 帯電器
60 積層装置
61 エンボスローラ
62 積層部
100 バージンパルプ
l ローション薬液
m マイクロカプセル
P 原紙
DESCRIPTION OF SYMBOLS 10 Production apparatus 20 Base paper supply apparatus 21 Secondary raw roll 22 Conveyance roller 23 Tension roller 30 Liquid application apparatus 31 Application unit 32 Sprayer 33 Back roller 40 Microcapsule application apparatus 41 Application unit 42 Microcapsule storage part 43 Spreading roller 44 Doctor blade 45 Anti-scattering roller 46 Discharge wire 47 Charger 60 Laminating device 61 Embossing roller 62 Laminating section 100 Virgin pulp l Lotion chemical m Microcapsule P Base paper

Claims (6)

  1.  衛生薄葉紙の原紙に対してマイクロカプセルを塗布するマイクロカプセル塗布装置と、
     衛生薄葉紙の原紙に対してローション薬液を塗布する液体塗布装置とを備え、
     前記マイクロカプセル塗布装置は、前記マイクロカプセルを静電塗布により前記原紙に塗布することを特徴とすることを特徴とする衛生薄葉紙の製造装置。
    A microcapsule applicator for applying microcapsules to a sanitary thin paper base;
    A liquid application device for applying a lotion chemical solution to a sanitary thin paper base,
    The microcapsule application device applies the microcapsule to the base paper by electrostatic application, and is characterized in that it is a sanitary thin paper manufacturing device.
  2.  前記液体塗布装置は、ローターダンプニング印刷装置であることを特徴とする請求項1記載の衛生薄葉紙の製造装置。 2. The sanitary thin paper manufacturing apparatus according to claim 1, wherein the liquid applying apparatus is a rotor dampening printing apparatus.
  3.  前記マイクロカプセルは、ウレタン、尿素-メラミン、尿素-ホルマリンのいずれかを主たる原料とすることを特徴とする請求項1又は2記載の衛生薄葉紙の製造装置。 3. The sanitary thin paper manufacturing apparatus according to claim 1 or 2, wherein the microcapsule is mainly made of urethane, urea-melamine, or urea-formalin.
  4.  衛生薄葉紙の原紙に対してマイクロカプセルを塗布するマイクロカプセル塗布工程と、
     衛生薄葉紙の原紙に対してローション薬液を塗布する液体塗布工程とを備え、
     前記マイクロカプセル塗布工程は、前記マイクロカプセルが静電塗布により前記原紙に塗布されることを特徴とする衛生薄葉紙の製造方法。
    A microcapsule application process for applying microcapsules to a sanitary thin paper base;
    A liquid application process for applying a lotion chemical to a sanitary thin paper base,
    In the microcapsule application step, the microcapsule is applied to the base paper by electrostatic application.
  5.  前記液体塗布工程は、ローターダンプニング印刷方式により行われることを特徴とする請求項4記載の衛生薄葉紙の製造方法。 The method for producing sanitary thin paper according to claim 4, wherein the liquid application step is performed by a rotor dampening printing method.
  6.  前記マイクロカプセル塗布工程は、ウレタン、尿素-メラミン、尿素-ホルマリンのいずれかを主たる原料とする前記マイクロカプセルの塗布が行われることを特徴とする請求項4又は5記載の衛生薄葉紙の製造方法。 6. The method for producing sanitary thin paper according to claim 4 or 5, wherein in the microcapsule coating step, the microcapsule is mainly coated with urethane, urea-melamine, or urea-formalin.
PCT/JP2017/007309 2016-03-31 2017-02-27 Production device for sanitary tissue paper and production method for sanitary tissue paper WO2017169416A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2016071952A JP6684135B2 (en) 2016-03-31 2016-03-31 Sanitary thin paper manufacturing apparatus and sanitary thin paper manufacturing method
JP2016-071952 2016-03-31

Publications (1)

Publication Number Publication Date
WO2017169416A1 true WO2017169416A1 (en) 2017-10-05

Family

ID=59963155

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/JP2017/007309 WO2017169416A1 (en) 2016-03-31 2017-02-27 Production device for sanitary tissue paper and production method for sanitary tissue paper

Country Status (2)

Country Link
JP (1) JP6684135B2 (en)
WO (1) WO2017169416A1 (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP6497431B1 (en) * 2017-12-01 2019-04-10 王子ホールディングス株式会社 Kitchen paper bundle manufacturing method and kitchen paper bundle manufacturing apparatus
JP7421729B2 (en) 2020-02-28 2024-01-25 愛媛県 Long-term retention sheet for aroma ingredients

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2003064393A (en) * 2001-08-29 2003-03-05 Toppan Forms Co Ltd Perfume composition containing fine particle of water- absorbing polymer carrying perfume
JP2003325372A (en) * 2002-05-14 2003-11-18 Crecia Corp Sanitary paper
JP2015016355A (en) * 2014-09-22 2015-01-29 大王製紙株式会社 Method of manufacturing tissue paper product

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2003064393A (en) * 2001-08-29 2003-03-05 Toppan Forms Co Ltd Perfume composition containing fine particle of water- absorbing polymer carrying perfume
JP2003325372A (en) * 2002-05-14 2003-11-18 Crecia Corp Sanitary paper
JP2015016355A (en) * 2014-09-22 2015-01-29 大王製紙株式会社 Method of manufacturing tissue paper product

Also Published As

Publication number Publication date
JP2017176684A (en) 2017-10-05
JP6684135B2 (en) 2020-04-22

Similar Documents

Publication Publication Date Title
JP4934474B2 (en) Lotion paper manufacturing method and manufacturing apparatus
JP5395101B2 (en) Toilet paper manufacturing method
JP5073957B2 (en) Manufacturing method and manufacturing equipment for household sanitary thin paper
JP4868620B2 (en) Tissue paper and tissue paper manufacturing method
JP2009183411A (en) Manufacturing method of sanitary paper
WO2017169416A1 (en) Production device for sanitary tissue paper and production method for sanitary tissue paper
JP4287438B2 (en) Thin paper containing chemicals
JP2006007218A (en) Method and apparatus for applying chemical liquid onto fiber web
JP5142343B2 (en) Production method of lotion paper
JP4868625B2 (en) Tissue paper and tissue paper manufacturing method
JP4783640B2 (en) Thin paper containing chemicals
JP2007204868A5 (en)
JP5898832B2 (en) Tissue paper
WO2017169415A1 (en) Production device for sanitary tissue paper and production method for sanitary tissue paper
AU2004297148B2 (en) Method for changing the orientation of the plies within a multi-ply product
JP4868622B2 (en) Tissue paper and tissue paper manufacturing method
JP6068787B2 (en) Tissue paper manufacturing method
MXPA06005122A (en) Method for changing the orientation of the plies within a multi-ply product

Legal Events

Date Code Title Description
NENP Non-entry into the national phase

Ref country code: DE

121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 17773961

Country of ref document: EP

Kind code of ref document: A1

122 Ep: pct application non-entry in european phase

Ref document number: 17773961

Country of ref document: EP

Kind code of ref document: A1