JP6702496B1 - LAMINATED PAPER, LAMINATED PAPER PAPER BASE, PAPER CONTAINER AND LAMINATED PAPER MANUFACTURING METHOD - Google Patents

LAMINATED PAPER, LAMINATED PAPER PAPER BASE, PAPER CONTAINER AND LAMINATED PAPER MANUFACTURING METHOD Download PDF

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JP6702496B1
JP6702496B1 JP2019235213A JP2019235213A JP6702496B1 JP 6702496 B1 JP6702496 B1 JP 6702496B1 JP 2019235213 A JP2019235213 A JP 2019235213A JP 2019235213 A JP2019235213 A JP 2019235213A JP 6702496 B1 JP6702496 B1 JP 6702496B1
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paper
laminated
base material
fatty acid
linear
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JP2020116944A (en
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啓史 山中
啓史 山中
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New Oji Paper Co Ltd
Oji Holdings Corp
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Oji Holdings Corp
Oji Paper Co Ltd
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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00Layered products comprising a layer of synthetic resin
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00Layered products comprising a layer of synthetic resin
    • B32B27/06Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material
    • B32B27/10Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material of paper or cardboard
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B65CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
    • B65DCONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
    • B65D5/00Rigid or semi-rigid containers of polygonal cross-section, e.g. boxes, cartons or trays, formed by folding or erecting one or more blanks made of paper
    • B65D5/42Details of containers or of foldable or erectable container blanks
    • B65D5/56Linings or internal coatings, e.g. pre-formed trays provided with a blow- or thermoformed layer
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B65CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
    • B65DCONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
    • B65D5/00Rigid or semi-rigid containers of polygonal cross-section, e.g. boxes, cartons or trays, formed by folding or erecting one or more blanks made of paper
    • B65D5/42Details of containers or of foldable or erectable container blanks
    • B65D5/62External coverings or coatings
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B65CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
    • B65DCONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
    • B65D65/00Wrappers or flexible covers; Packaging materials of special type or form
    • B65D65/38Packaging materials of special type or form
    • B65D65/40Applications of laminates for particular packaging purposes
    • 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
    • D21H11/00Pulp or paper, comprising cellulose or lignocellulose fibres of natural origin only
    • 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
    • D21H17/00Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
    • D21H17/03Non-macromolecular organic compounds
    • D21H17/05Non-macromolecular organic compounds containing elements other than carbon and hydrogen only
    • D21H17/06Alcohols; Phenols; Ethers; Aldehydes; Ketones; Acetals; Ketals
    • 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
    • D21H17/00Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
    • D21H17/03Non-macromolecular organic compounds
    • D21H17/05Non-macromolecular organic compounds containing elements other than carbon and hydrogen only
    • D21H17/14Carboxylic acids; Derivatives thereof
    • 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
    • D21H27/00Special paper not otherwise provided for, e.g. made by multi-step processes
    • D21H27/30Multi-ply
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02WCLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
    • Y02W30/00Technologies for solid waste management
    • Y02W30/50Reuse, recycling or recovery technologies
    • Y02W30/80Packaging reuse or recycling, e.g. of multilayer packaging

Landscapes

  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Laminated Bodies (AREA)
  • Paper (AREA)
  • Wrappers (AREA)
  • Cartons (AREA)

Abstract

【課題】紙基材と熱可塑性樹脂層との剥離が容易であり、原料をリサイクルすることが容易なラミネート紙と、当該ラミネート紙用紙基材、当該ラミネート紙を用いた紙容器および当該ラミネート紙の製造方法を提供する。【解決手段】セルロースパルプを主成分とする紙基材と、当該紙基材の少なくとも一方の面上に積層された熱可塑性樹脂層とを有する紙容器用ラミネート紙であって、前記紙基材は、直鎖脂肪酸および直鎖アルコールの少なくとも1種を含有し、前記直鎖脂肪酸および前記直鎖アルコールの融点が80〜100℃であり、前記紙基材中の前記直鎖脂肪酸および前記直鎖アルコールの含有量の合計が100〜2500ppmであることを特徴とする紙容器用ラミネート紙である。また当該紙容器用ラミネート紙用紙基材、当該紙容器用ラミネート紙を用いた紙容器および当該紙容器用ラミネート紙の製造方法である。【選択図】なしPROBLEM TO BE SOLVED: To easily separate a paper base material and a thermoplastic resin layer, and to easily recycle raw materials, a laminated paper base material, a paper container using the laminated paper, and the laminated paper. A method of manufacturing the same is provided. A laminated paper for a paper container having a paper base material containing cellulose pulp as a main component and a thermoplastic resin layer laminated on at least one surface of the paper base material. Contains at least one of a linear fatty acid and a linear alcohol, the melting point of the linear fatty acid and the linear alcohol is 80 to 100° C., and the linear fatty acid and the linear chain in the paper substrate are A laminated paper for a paper container, wherein the total content of alcohol is 100 to 2500 ppm. The present invention also relates to a laminated paper base material for the paper container, a paper container using the laminated paper for the paper container, and a method for manufacturing the laminated paper for the paper container. [Selection diagram] None

Description

本発明は、ラミネート紙、ラミネート紙用紙基材、紙容器およびラミネート紙の製造方法に関する。 TECHNICAL FIELD The present invention relates to a laminated paper, a laminated paper paper base material, a paper container, and a laminated paper manufacturing method.

牛乳パック等に利用される液体用紙容器では、パルプ繊維を主体とする紙基材にポリエチレン等の熱可塑性樹脂層をラミネートし、耐水性を付与させたラミネート紙が多く用いられている。この種の液体用紙容器は、使用後に紙基材と熱可塑性樹脂層とに分離し、紙分は古紙原料として、また熱可塑性樹脂層のうち比較的純度の高いものはRPF(Refuse Paper & Plastic Fuel)(固形燃料)や再生プラスチックの原料として回収利用されることがある。しかしながら、紙基材から熱可塑性樹脂層を剥離することは一般に容易ではないため、リサイクルの効率は必ずしも高くはなく、さらなる改善が求められていた。 In liquid paper containers used for milk packs and the like, laminated paper in which a thermoplastic resin layer such as polyethylene is laminated on a paper base material mainly composed of pulp fibers to impart water resistance is often used. This type of liquid paper container is separated into a paper base material and a thermoplastic resin layer after use, the paper component is used as a waste paper raw material, and the thermoplastic resin layer of relatively high purity is RPF (Refuse Paper & Plastic). It may be recovered and used as a raw material for fuel (solid fuel) and recycled plastic. However, since it is generally not easy to peel the thermoplastic resin layer from the paper base material, the recycling efficiency is not always high, and further improvement has been demanded.

そこで、液体用紙容器の原料をリサイクルするための技術が開発されている。例えば特許文献1では、オレフィン系樹脂からなる最外層、紙基材層、接着調整層、接着樹脂層、バリア層、樹脂フィルム層、オレフィン系樹脂を含む最内層を有する積層体からなり、胴部のうち帯状分離体と胴部切目線との間の領域において少なくとも最外層および紙基材層をバリア層から剥離する液体用紙容器が開示されている。 Therefore, a technique for recycling the raw material of the liquid paper container has been developed. For example, in Patent Document 1, the outermost layer made of an olefin resin, a paper base layer, an adhesion adjusting layer, an adhesive resin layer, a barrier layer, a resin film layer, a laminate having an innermost layer containing an olefin resin, There is disclosed a liquid paper container in which at least the outermost layer and the paper base material layer are separated from the barrier layer in the region between the strip-shaped separator and the body score line.

また特許文献2では、ゲーブルトップ型容器の頂部形成板の側端角部の紙層に紙間強化剤を含浸させ、紙を主体とする層とプラスチックを主体とする層とに剥離させるきっかけを作りやすくした構成の液体用紙容器が開示されている。 Further, in Patent Document 2, there is an opportunity for impregnating a paper layer at a side end corner portion of a top forming plate of a gable top type container with a paper strengthening agent to separate the paper-based layer from the plastic-based layer. A liquid paper container having a structure that is easy to make is disclosed.

特開2012−166796号公報JP, 2012-166796, A 特開2000−185729号公報JP, 2000-185729, A

特許文献1の液体用紙容器は、紙基材層とバリア層の剥離が容易な液体用紙容器ではあるが、多数の層からなり、剥離性向上のために切り目加工が施されることから、耐久性等において改良の余地を有するものであった。また、特許文献2の液体用紙容器も、紙を主体とする層とプラスチックを主体とする層を剥離する際のきっかけとなる箇所を設けた液体用紙容器であるが、同きっかけとなる箇所は紙容器の一部分に過ぎず、紙容器のほとんどの部分の接着は強固なままであるため、リサイクル性等において改良の余地を有するものであった。 The liquid paper container of Patent Document 1 is a liquid paper container in which the paper base material layer and the barrier layer can be easily peeled off, but it is composed of a number of layers and is cut to improve the peeling property. There was room for improvement in sex. Further, the liquid paper container of Patent Document 2 is also a liquid paper container provided with a location that serves as a trigger when the layer mainly composed of paper and the layer mainly composed of plastic are peeled off. Since only a part of the container and most of the paper container remains firmly adhered, there is room for improvement in recyclability and the like.

本発明は、上記のような状況に鑑みてなされたものである。すなわち、本発明の課題は、紙基材と熱可塑性樹脂層との剥離が容易であり、原料をリサイクルすることが容易なラミネート紙と、当該ラミネート紙用紙基材、当該ラミネート紙を用いた紙容器および当該ラミネート紙の製造方法を提供することである。 The present invention has been made in view of the above situation. That is, an object of the present invention is to provide a laminated paper in which the paper base material and the thermoplastic resin layer can be easily peeled off and the raw material can be easily recycled, the laminated paper paper base material, and the paper using the laminated paper. A container and a method for manufacturing the laminated paper.

本発明者らは、特定の直鎖脂肪酸または直鎖アルコールを所定量含有した紙基材について検討を進めた。その結果、特定の種類の直鎖脂肪酸または直鎖アルコールを所定量含有した紙基材は、製造時は熱可塑性樹脂層と強固に密着するが、その後当該成分が経時的に紙基材の表面付近にブリードして、紙基材と熱可塑性樹脂層との剥離が容易となることを見出した。本発明はこのような知見を基に完成するに至ったものである。すなわち、本発明は、以下のような構成を有している。 The present inventors proceeded with the study on a paper base material containing a specific amount of a specific linear fatty acid or linear alcohol. As a result, the paper base material containing a specific amount of a specific type of linear fatty acid or linear alcohol firmly adheres to the thermoplastic resin layer at the time of production, but after that, the component concerned surface of the paper base material over time. It was found that the paper base material and the thermoplastic resin layer can be easily peeled off by bleeding in the vicinity. The present invention has been completed based on these findings. That is, the present invention has the following configurations.

(1)セルロースパルプを主成分とする紙基材と、当該紙基材の少なくとも一方の面上に積層された熱可塑性樹脂層とを有する紙容器用ラミネート紙であって、前記紙基材は、直鎖脂肪酸および直鎖アルコールの少なくとも1種を含有し、前記直鎖脂肪酸および前記直鎖アルコールの融点が80〜100℃であり、前記紙基材中の前記直鎖脂肪酸および前記直鎖アルコールの含有量の合計が100〜2500ppmであることを特徴とする紙容器用ラミネート紙。 (1) A laminated paper for a paper container, comprising a paper base material containing cellulose pulp as a main component, and a thermoplastic resin layer laminated on at least one surface of the paper base material, wherein the paper base material is At least one of a straight-chain fatty acid and a straight-chain alcohol, the straight-chain fatty acid and the straight-chain alcohol have a melting point of 80 to 100° C., and the straight-chain fatty acid and the straight-chain alcohol in the paper base material. Laminated paper for paper containers, wherein the total content of the above is 100 to 2500 ppm.

(2)前記直鎖脂肪酸の炭素数が24、26または28であり、前記直鎖アルコールの炭素数が26または28である前記(1)に記載の紙容器用ラミネート紙。 (2) The laminated paper for a paper container according to (1), wherein the linear fatty acid has 24, 26 or 28 carbon atoms, and the linear alcohol has 26 or 28 carbon atoms.

(3)前記紙基材が前記直鎖脂肪酸および前記直鎖アルコールの両者を含有し、前記直鎖脂肪酸の含有量に対する前記直鎖アルコールの含有量の比率が、3.0〜33.3%である前記(1)または前記(2)に記載の紙容器用ラミネート紙。 (3) The paper base material contains both the linear fatty acid and the linear alcohol, and the ratio of the linear alcohol content to the linear fatty acid content is 3.0 to 33.3%. The laminated paper for a paper container according to (1) or (2) above.

(4)カヤーニファイバーラボで測定される前記紙基材の離解原料の繊維粗度が0.020〜0.18mg/mである前記(1)〜(3)のいずれか1項に記載の紙容器用ラミネート紙。 (4) The paper according to any one of (1) to (3), wherein the fiber roughness of the disaggregation raw material of the paper base material is 0.020 to 0.18 mg/m, as measured by Kajaani Fiber Lab. Laminated paper for containers.

(5)坪量が150〜500g/mである前記(1)〜(4)のいずれか1項に記載の紙容器用ラミネート紙。 (5) The laminated paper for paper containers according to any one of (1) to (4), which has a basis weight of 150 to 500 g/m 2 .

(6)前記紙基材が多層紙である前記(1)〜(5)のいずれか1項に記載の紙容器用ラミネート紙。 (6) The laminated paper for paper containers according to any one of (1) to (5), wherein the paper base material is a multi-layered paper.

(7)セルロースパルプを主成分とする紙容器用ラミネート紙用紙基材であって、直鎖脂肪酸および直鎖アルコールの少なくとも1種を含有し、前記直鎖脂肪酸および前記直鎖アルコールの融点が80〜100℃であり、前記直鎖脂肪酸および前記直鎖アルコールの含有量の合計が100〜2500ppmであることを特徴とする紙容器用ラミネート紙用紙基材。 (7) A laminated paper base material for paper containers, which comprises cellulose pulp as a main component, and contains at least one of a linear fatty acid and a linear alcohol, and the melting point of the linear fatty acid and the linear alcohol is 80. It is -100 degreeC, and the total content of the said linear fatty acid and the said linear alcohol is 100-2500 ppm, The laminated paper paper base material for paper containers characterized by the above-mentioned.

(8)多層紙である前記(7)に記載の紙容器用ラミネート紙用紙基材。 (8) The laminated paper base material for paper containers according to (7), which is a multi-layered paper.

(9)前記(1)〜(6)のいずれか1項に記載の紙容器用ラミネート紙を用いた紙容器。 (9) A paper container using the laminated paper for paper container according to any one of (1) to (6).

(10)液体用である前記(9)に記載の紙容器。 (10) The paper container according to (9), which is for liquids.

(11)前記(1)〜(6)のいずれか1項に記載の紙容器用ラミネート紙の製造方法であって、セルロースパルプを主成分とする紙基材の抄紙工程と、前記紙基材の少なくとも一方の面上に熱可塑性樹脂層を積層するラミネート工程とを有し、前記抄紙工程および前記ラミネート工程の少なくともいずれかの工程で、前記紙基材に100℃以上に加熱された物を接触させることを特徴とする紙容器用ラミネート紙の製造方法。 (11) A method for producing a laminated paper for a paper container according to any one of (1) to (6), which comprises a step of making a paper base material containing cellulose pulp as a main component, and the paper base material. And a laminating step of laminating a thermoplastic resin layer on at least one surface of the paper making step and at least one of the laminating steps A method for producing a laminated paper for a paper container, which is characterized by bringing them into contact with each other.

(12)前記紙基材が多層紙であって、前記抄紙工程において、多層抄き用抄紙機を用いて前記紙基材を抄紙することを特徴とする前記(11)に記載の紙容器用ラミネート紙の製造方法。 (12) The paper container according to (11), wherein the paper base material is a multi-layer paper, and the paper base material is made by using a multi-layer paper machine in the paper making step. Laminated paper manufacturing method.

本発明のラミネート紙および当該ラミネート紙を用いた紙容器は、紙基材と熱可塑性樹脂層との剥離が容易であり、原料をリサイクルすることが容易である。 In the laminated paper of the present invention and the paper container using the laminated paper, the paper base material and the thermoplastic resin layer can be easily peeled off, and the raw materials can be easily recycled.

本発明の実施形態について以下説明する。ただし、本発明の実施形態は、以下の実施形態に限定されるものではない。 Embodiments of the present invention will be described below. However, the embodiments of the present invention are not limited to the following embodiments.

本実施形態のラミネート紙は、セルロースパルプを主成分とする紙基材と、当該紙基材の少なくとも一方の面上に積層された熱可塑性樹脂層とを有する。以下、ラミネート紙を構成する各素材について説明する。 The laminated paper of the present embodiment has a paper base material containing cellulose pulp as a main component, and a thermoplastic resin layer laminated on at least one surface of the paper base material. Hereinafter, each material constituting the laminated paper will be described.

[紙基材]
紙基材はセルロースパルプを主成分とする。ここで主成分とは、紙基材を構成する成分のうち50質量%以上を占める成分をいう。セルロースパルプとしては、木材パルプ、非木材パルプ等を挙げることができる。木材パルプとしては、例えば、針葉樹材の晒クラフトパルプ(NBKP)、針葉樹クラフトパルプ(NKP)、広葉樹材の晒クラフトパルプ(LBKP)、広葉樹クラフトパルプ(LKP)等の木材系パルプ、サルファイトパルプ(SP)、溶解パルプ(DP)、ソーダパルプ(AP)、未晒しクラフトパルプ(UKP)、酸素漂白クラフトパルプ(OKP)等の化学パルプ等が挙げられる。また、セミケミカルパルプ(SCP)、ケミグラウンドウッドパルプ(CGP)等の半化学パルプ、砕木パルプ(GP)、サーモメカニカルパルプ(TMP、BCTMP)等の機械パルプが挙げられる。非木材パルプでは、麻やバガス、綿等が挙げられる。これらのパルプは、1種単独または2種以上を組み合わせて使用することができる。紙基材を構成するパルプとしては、品質やコストの面から、LKPであるアカシア材やユーカリ材等の木材系パルプが適している。なお、原料パルプはバージンパルプに限定されない。
[Paper substrate]
The paper base material is mainly composed of cellulose pulp. Here, the main component means a component accounting for 50% by mass or more of the components constituting the paper base material. Examples of the cellulose pulp include wood pulp and non-wood pulp. Examples of the wood pulp include bleached kraft pulp of softwood (NBKP), softwood kraft pulp (NKP), bleached kraft pulp of hardwood (LBKP), hardwood kraft pulp (LKP), and other wood pulp, sulfite pulp ( Examples thereof include chemical pulp such as SP), dissolving pulp (DP), soda pulp (AP), unbleached kraft pulp (UKP), and oxygen bleached kraft pulp (OKP). Further, semi-chemical pulps such as semi-chemical pulp (SCP) and chemi-groundwood pulp (CGP), mechanical pulps such as groundwood pulp (GP) and thermomechanical pulp (TMP, BCTMP) can be mentioned. Examples of the non-wood pulp include hemp, bagasse, cotton and the like. These pulps may be used alone or in combination of two or more. From the viewpoint of quality and cost, wood pulp such as acacia lumber and eucalyptus lumber, which are LKP, are suitable as the pulp constituting the paper base material. The raw material pulp is not limited to virgin pulp.

カヤーニファイバーラボで測定される紙基材の離解原料の繊維粗度は、0.020〜0.18mg/mであることが好ましい。紙基材の離解方法は、JISP8220−1:2012 に準拠して行う。一般に、繊維粗度が小さい方が繊維が細く、紙基材中に繊維が密に充填されるため、直鎖脂肪酸や直鎖アルコールのブリーディングが均一となるほか、紙基材の表面平滑性が向上することでラミネートの均一な接着性が向上して好ましい。また、紙基材の表面平滑性が向上することで紙基材表面への印刷適性が向上するとともに、ラミネート後の表面平滑性も向上することから、ラミネート表面への印刷適性も向上する。しかし、繊維粗度が0.020mg/m未満になると、紙の厚みが出にくくなる。また、紙基材を構成する繊維の投影長さ加重平均繊維長は0.40〜2.00mmであることが好ましい。繊維の平均繊維長は、JIS P8226:2006に準拠して測定される。 The fiber roughness of the disaggregation raw material of the paper base material, which is measured by Kajaani Fiber Lab, is preferably 0.020 to 0.18 mg/m. The disaggregation method of the paper base material is performed according to JIS P8220-1:2012. Generally, the smaller the fiber roughness is, the finer the fibers are, and the fibers are densely packed in the paper base material, so that the bleeding of linear fatty acids and linear alcohols is uniform and the surface smoothness of the paper base material is improved. It is preferable that the uniform adhesion of the laminate is improved by the improvement. Further, since the surface smoothness of the paper base material is improved, the printability on the surface of the paper base material is improved, and the surface smoothness after lamination is also improved, so that the printability on the laminate surface is also improved. However, if the fiber roughness is less than 0.020 mg/m, it is difficult to obtain the paper thickness. Further, the projected length weighted average fiber length of the fibers constituting the paper base material is preferably 0.40 to 2.00 mm. The average fiber length of the fibers is measured according to JIS P8226:2006.

紙基材は、単層構成の紙であってもよいし、2以上の層からなる多層構成の紙(多層紙)であってもよい。多層紙の場合、層の数は2以上6以下であることが好ましく、3以上5以下であることがさらに好ましい。多層紙では各層の原料配合や坪量、抄造条件等を任意に調整することができ、層間には層間接着を強化する澱粉や紙力増強剤などを含有させてもよい。このような操作により直鎖脂肪酸や直鎖アルコールのブリーディングを調節できるほか、地合や平滑度を向上させ、表面性を向上させることができる。 The paper base material may be a single-layered paper or a multi-layered paper (multi-layered paper) composed of two or more layers. In the case of multilayer paper, the number of layers is preferably 2 or more and 6 or less, and more preferably 3 or more and 5 or less. In the multi-layered paper, the raw material composition of each layer, the basis weight, the papermaking conditions and the like can be adjusted as desired, and a starch or a paper-strengthening agent which enhances interlayer adhesion may be contained between the layers. By such an operation, the bleeding of the linear fatty acid or the linear alcohol can be adjusted, and the texture and the smoothness can be improved to improve the surface property.

(直鎖脂肪酸および直鎖アルコール)
紙基材は、直鎖脂肪酸および直鎖アルコールの少なくとも1種を含有する。直鎖脂肪酸とは、直鎖状のアルキル基を有する1価のカルボン酸のことである。また、直鎖アルコールとは、直鎖状のアルキル基を有する1価のアルコールのことである。
(Straight chain fatty acid and straight chain alcohol)
The paper base material contains at least one of a linear fatty acid and a linear alcohol. A straight-chain fatty acid is a monovalent carboxylic acid having a straight-chain alkyl group. The linear alcohol is a monovalent alcohol having a linear alkyl group.

セルロースパルプは一般に、直鎖脂肪酸や直鎖アルコールを含有している。植物内においては、一般に、炭素数が2の酢酸を出発物質として直鎖脂肪酸や直鎖アルコールが合成されている。そのため、合成された脂肪酸やアルコールの炭素数は偶数となる。 Cellulose pulp generally contains straight chain fatty acids and straight chain alcohols. In plants, linear fatty acids and linear alcohols are generally synthesized starting from acetic acid having 2 carbon atoms. Therefore, the carbon number of the synthesized fatty acid or alcohol is even.

本発明者は、直鎖脂肪酸や直鎖アルコールを含有する紙基材と熱可塑性樹脂層とからなるラミネート紙の剥離挙動を検討した。その結果、紙基材中に融点が80〜100℃である直鎖脂肪酸または直鎖アルコールが存在すると、ラミネート紙製造後の時間の経過とともに、当該直鎖脂肪酸または直鎖アルコールが紙基材の表面付近にブリーディングする(表面に遊離する)ことを見出した。さらに当該直鎖脂肪酸または直鎖アルコールは、紙基材の表面付近にブリーディングした後、熱可塑性樹脂層との界面に侵入してくる。その結果、紙基材と熱可塑性樹脂層とのラミネート後、ある程度の時間が経過すると、紙基材と熱可塑性樹脂層との剥離が容易となることを見出した。 The present inventor investigated the peeling behavior of a laminated paper comprising a paper base material containing a linear fatty acid or a linear alcohol and a thermoplastic resin layer. As a result, when a linear fatty acid or a linear alcohol having a melting point of 80 to 100° C. is present in the paper base material, the linear fatty acid or the linear alcohol is converted into a paper base material with the lapse of time after the production of laminated paper. It was found to bleed near the surface (release to the surface). Further, the straight-chain fatty acid or straight-chain alcohol bleeds near the surface of the paper base material and then enters the interface with the thermoplastic resin layer. As a result, it has been found that, after laminating the paper base material and the thermoplastic resin layer, the paper base material and the thermoplastic resin layer are easily peeled off after a certain amount of time has elapsed.

本実施形態において、直鎖脂肪酸および直鎖アルコールの融点は80〜100℃である。直鎖脂肪酸および直鎖アルコールの融点が前記温度範囲内にあると、紙基材の製造時に用いられる100℃以上に加熱されたドライヤー等の装置、あるいはラミネート工程で100℃以上に加熱溶融された熱可塑性樹脂の熱で溶けるため、紙基材内に均一に分布させることができる。また、当該直鎖脂肪酸および直鎖アルコールは、経時的にブリーディングするため、紙基材と熱可塑性樹脂層との剥離が容易となる。融点が80〜100℃である直鎖脂肪酸とは、例えば、炭素数22のベヘン酸(融点80℃)、炭素数24のリグノセリン酸(融点84℃)、炭素数26のヘキサコサン酸(融点88℃)、炭素数28のオクタコサン酸(融点91℃)、炭素数30のトリアコンタン酸(融点94℃)である。一方、融点が80〜100℃である直鎖アルコールとは、例えば、炭素数26のヘキサコサノール(融点80℃)、炭素数28のオクタコサノール(融点83℃)、炭素数30のトリアコンタノール(融点86℃)である。ここで、個々の直鎖脂肪酸および直鎖アルコールの融点は、DSC法によって求められる。 In the present embodiment, the melting point of the linear fatty acid and the linear alcohol is 80 to 100°C. When the melting points of the straight-chain fatty acid and the straight-chain alcohol are within the above-mentioned temperature range, a device such as a dryer heated to 100° C. or higher used in the production of the paper substrate, or heated and melted to 100° C. or higher in the laminating step Since it is melted by the heat of the thermoplastic resin, it can be uniformly distributed in the paper base material. Further, since the linear fatty acid and the linear alcohol bleed over time, the paper base material and the thermoplastic resin layer can be easily separated from each other. Linear fatty acids having a melting point of 80 to 100° C. include, for example, behenic acid having 22 carbon atoms (melting point 80° C.), lignoceric acid having 24 carbon atoms (melting point 84° C.), hexacosanoic acid having 26 carbon atoms (melting point 88° C. ), octacosanoic acid having 28 carbon atoms (melting point 91° C.), and triacontanoic acid having 30 carbon atoms (melting point 94° C.). On the other hand, the linear alcohol having a melting point of 80 to 100° C. means, for example, hexacosanol having a carbon number of 26 (melting point 80° C.), octacosanol having a carbon number of 28 (melting point 83° C.), and triacontanol having a carbon number of 30 ( Melting point 86°C). Here, the melting points of the individual linear fatty acids and linear alcohols are obtained by the DSC method.

直鎖脂肪酸および直鎖アルコールの融点が低過ぎると、ドライヤーやラミネート工程でブリーディングが過度に促進されるため、ラミネートの接着不良が生じ易くなる。一方、融点が高過ぎると、ドライヤー等の熱で融解しないため、紙基材内において直鎖脂肪酸および直鎖アルコールの分布が均一化されず、当該成分同士が集合化して固まるため、異物化し易くなる。 If the melting point of the straight-chain fatty acid and the straight-chain alcohol is too low, bleeding is excessively promoted in the dryer or the laminating process, so that the adhesion failure of the laminate is likely to occur. On the other hand, if the melting point is too high, it will not be melted by the heat of a drier or the like, so that the distribution of the linear fatty acid and the linear alcohol will not be uniform in the paper base material, and the components will be aggregated and hardened, so that it easily becomes a foreign substance. Become.

また、紙基材中の直鎖脂肪酸および直鎖アルコールの含有量(質量)の合計は、100〜2500ppmであり、150〜2400ppmであることが好ましい。ここで、直鎖脂肪酸および直鎖アルコールの含有量の合計とは、融点が80〜100℃である直鎖脂肪酸および直鎖アルコールの含有量の合計である。ここで、直鎖脂肪酸とは、融点が80〜100℃である直鎖脂肪酸の1種類のみからなっていてもよいし、融点が80〜100℃である複数種類の直鎖脂肪酸を含有する混合物であってもよい。同様に、直鎖アルコールとは、融点が80〜100℃である直鎖アルコールの1種類のみからなっていてもよいし、融点が80〜100℃である複数種類の直鎖アルコールを含有する混合物であってもよい。直鎖脂肪酸または直鎖アルコールの含有量は、後記する方法で定量することができる。尚、紙基材は、本発明の効果に支障を与えない範囲内であれば、融点が80〜100℃から外れる直鎖脂肪酸または直鎖アルコールを含有していてもよい。 The total content (mass) of linear fatty acid and linear alcohol in the paper substrate is 100 to 2500 ppm, preferably 150 to 2400 ppm. Here, the total content of the linear fatty acid and the linear alcohol is the total content of the linear fatty acid and the linear alcohol having a melting point of 80 to 100°C. Here, the linear fatty acid may consist of only one type of linear fatty acid having a melting point of 80 to 100°C, or a mixture containing a plurality of types of linear fatty acid having a melting point of 80 to 100°C. May be Similarly, the linear alcohol may consist of only one type of linear alcohol having a melting point of 80 to 100°C, or a mixture containing a plurality of linear alcohols having a melting point of 80 to 100°C. May be The content of linear fatty acid or linear alcohol can be quantified by the method described below. The paper substrate may contain a linear fatty acid or a linear alcohol having a melting point of 80 to 100°C as long as the effect of the present invention is not impaired.

直鎖脂肪酸と直鎖アルコールの含有量の合計が少な過ぎると、ブリーディングによって紙基材と熱可塑性樹脂層との剥離が容易となる効果が出にくい。一方、直鎖脂肪酸と直鎖アルコールの含有量の合計が多過ぎると、脂肪酸塩(カルシウム塩など)の形で製造装置内に蓄積して、紙基材に汚れが生じるおそれがある。また、紙基材中に直鎖脂肪酸と直鎖アルコールの含有量の合計が多過ぎると、これら化合物が紙基材中あるいは紙基材表面に凝集異物となって析出し、紙基材の表面平滑性が低下するおそれがある。凝集異物が析出すると、ラミネート接着の均一性も低下するため、ラミネート表面の平滑性も低下する。 If the total content of the straight chain fatty acid and the straight chain alcohol is too small, the effect of facilitating the peeling of the paper base material and the thermoplastic resin layer due to bleeding is difficult to be obtained. On the other hand, if the total content of the linear fatty acid and the linear alcohol is too large, the fatty acid salt (calcium salt or the like) may be accumulated in the manufacturing apparatus and the paper substrate may be soiled. Further, if the total content of the linear fatty acid and the linear alcohol in the paper base material is too large, these compounds will be deposited in the paper base material or on the surface of the paper base material as aggregated foreign matter, and the surface of the paper base material will be precipitated. The smoothness may decrease. When the coagulated foreign matter is deposited, the uniformity of the adhesion of the laminate is also reduced, and the smoothness of the laminate surface is also reduced.

紙基材中の直鎖脂肪酸および直鎖アルコールの融点が前記温度範囲内にあり、また前記含有量で存在すると、ラミネート紙の製造時には、紙基材と熱可塑性樹脂層との接着性に問題はない。しかし、ラミネート紙の製造後、紙容器として使用され、商品寿命が終了した頃に、直鎖脂肪酸または直鎖アルコールが紙基材の表面付近にブリーディングしてきて、紙基材と熱可塑性樹脂層との剥離が容易となるように制御することができる。 When the melting point of the straight-chain fatty acid and the straight-chain alcohol in the paper base material is within the above-mentioned temperature range and the above-mentioned content is present, there is a problem in the adhesiveness between the paper base material and the thermoplastic resin layer during the production of laminated paper. There is no. However, after the laminated paper is manufactured, it is used as a paper container, and at the end of the product life, linear fatty acid or linear alcohol bleeds near the surface of the paper base material, and the paper base material and the thermoplastic resin layer Can be controlled so that peeling can be facilitated.

融点が80〜100℃である直鎖脂肪酸は、炭素数が24、26または28であることが好ましい。また、融点が80〜100℃である直鎖アルコールは、炭素数が24、26または28であることが好ましい。炭素数が24、26または28である直鎖脂肪酸とは、炭素数24、26および28からなる群より選択される炭素数の1価の直鎖脂肪酸のことである。また、炭素数が24、26または28である直鎖アルコールとは、炭素数24、26および28からなる群より選択される炭素数の1価の直鎖アルコールのことである。 The linear fatty acid having a melting point of 80 to 100° C. preferably has 24, 26 or 28 carbon atoms. The linear alcohol having a melting point of 80 to 100° C. preferably has 24, 26 or 28 carbon atoms. The straight chain fatty acid having 24, 26 or 28 carbon atoms is a monovalent straight chain fatty acid having a carbon number selected from the group consisting of 24, 26 and 28 carbon atoms. The linear alcohol having 24, 26 or 28 carbon atoms is a monovalent linear alcohol having a carbon number selected from the group consisting of 24, 26 and 28 carbon atoms.

紙基材の原料となるセルロースパルプに含まれる直鎖脂肪酸または直鎖アルコールの量は、パルプ原料となる木材チップを蒸解し繊維を回収する工程、洗浄する工程、漂白する工程、漂白後の洗浄工程、抄紙する工程、塗工する工程のいずれか、または複数の工程において調整することができる。例えば漂白後の洗浄工程におけるアルカリ添加や、マイクロタルク等の吸油性粒子やピッチコントロール剤等の分散剤添加により、紙基材の原料となるセルロースパルプに含まれる直鎖脂肪酸または直鎖アルコールの量を調整することができる。 The amount of linear fatty acid or linear alcohol contained in the cellulose pulp, which is the raw material for the paper base material, depends on the steps of cooking wood chips, which is the raw material for pulp, and recovering the fibers, washing, bleaching, and washing after bleaching. It can be adjusted in any one of a process, a paper making process, a coating process, or a plurality of processes. For example, the amount of straight-chain fatty acid or straight-chain alcohol contained in the cellulose pulp, which is a raw material of the paper base material, by addition of alkali in the washing step after bleaching, addition of oil-absorbing particles such as microtalc, and dispersant such as pitch control agent. Can be adjusted.

また、セルロースパルプの原料となる樹種の中には、炭素数が24、26または28である直鎖脂肪酸または直鎖アルコールを多く含有する樹種が存在する。例えば、アカシアなどである。そのため、これらの直鎖脂肪酸または直鎖アルコールを多く含有する樹種のパルプを紙基材の原料として適当量用いることによって、紙基材中の直鎖脂肪酸および直鎖アルコールの含有量を上記の所定量とすることができる。 In addition, among tree species as a raw material of cellulose pulp, there are tree species containing a large amount of linear fatty acids or linear alcohols having 24, 26 or 28 carbon atoms. For example, acacia. Therefore, the content of the linear fatty acid and the linear alcohol in the paper base is adjusted to the above range by using the pulp of the tree species containing a large amount of these linear fatty acids or the linear alcohol as a raw material of the paper base. It can be quantified.

直鎖脂肪酸の含有量に対する直鎖アルコールの含有量の比率は、3.0〜33.3%であることが好ましく、4.0〜30.0%であることがより好ましい。直鎖脂肪酸が多過ぎると、カルシウム塩等の形で製造装置内に蓄積して、紙基材の汚れにつながるおそれがある。一方、直鎖脂肪酸が少な過ぎると界面活性作用が不足して、ブリーディングが十分ではなくなるおそれがある。 The ratio of the content of the linear alcohol to the content of the linear fatty acid is preferably 3.0 to 33.3%, more preferably 4.0 to 30.0%. If the amount of the linear fatty acid is too large, it may accumulate in the manufacturing apparatus in the form of calcium salt or the like, which may lead to stain of the paper substrate. On the other hand, if the amount of the linear fatty acid is too small, the surfactant effect will be insufficient and bleeding may be insufficient.

紙基材に直鎖脂肪酸および直鎖アルコールを含有させる方法は特に限定されず、例えば以下のような方法がある。これらの中では、(1)の方法が、従来の製造プロセスを変える必要がないため、好ましい。
(1)上記の直鎖脂肪酸および直鎖アルコールを多く含有する樹種のパルプを紙基材の原料として用いる方法。
(2)パルプの製造工程または紙基材の抄紙工程のいずれかの工程で直鎖脂肪酸および直鎖アルコール、またはそれら成分を含む薬剤を所定量添加する方法。
(3)紙基材の抄紙後に直鎖脂肪酸および直鎖アルコール、またはそれら成分を含む薬剤を所定量含浸させる方法。
The method for incorporating the straight-chain fatty acid and the straight-chain alcohol into the paper base material is not particularly limited, and examples thereof include the following methods. Among these, the method (1) is preferable because it is not necessary to change the conventional manufacturing process.
(1) A method of using the pulp of a tree species containing a large amount of the above-mentioned straight chain fatty acid and straight chain alcohol as a raw material for a paper base material.
(2) A method of adding a predetermined amount of a chemical agent containing a straight-chain fatty acid and a straight-chain alcohol, or a component thereof, in any of the pulp manufacturing process and the paper-making paper making process.
(3) A method of impregnating a predetermined amount of a straight-chain fatty acid and a straight-chain alcohol, or a chemical containing these components, after paper-making a paper substrate.

紙基材を抄紙する際に、各種内添助剤を必要に応じて適宜選択して使用することが可能である。内添助剤の例としては、サイズ剤、歩留まり向上剤、ろ水度向上剤、嵩高剤、紙力向上剤、カチオン化澱粉などの各種澱粉類、硫酸バンド、着色染料、着色顔料、蛍光増白剤、pH調整剤、ピッチコントロール剤、防腐剤、スライムコントロール剤等が挙げられる。また、紙基材を抄紙する際には、填料を配合しても良い。填料は製紙分野で一般に使用されている填料が使用可能であり、特に限定されない。例えば、填料としてタルク等の無機鉱物を用いることで、紙基材中に含まれる直鎖脂肪酸または直鎖アルコールを適度に吸着させ、ブリーディングを調整することができる。 When making a paper substrate, various internal addition aids can be appropriately selected and used as necessary. Examples of the internal additive aids include sizing agents, yield improving agents, freeness improving agents, bulking agents, paper strength improving agents, various starches such as cationized starch, sulfuric acid bands, coloring dyes, coloring pigments, and fluorescence increasing agents. Examples include whitening agents, pH adjusters, pitch control agents, preservatives, slime control agents, and the like. Further, a filler may be blended when making the paper base material. The filler may be any filler commonly used in the papermaking field and is not particularly limited. For example, by using an inorganic mineral such as talc as the filler, the linear fatty acid or linear alcohol contained in the paper substrate can be appropriately adsorbed to adjust the bleeding.

紙基材の坪量は、特に限定されるものではないが、150〜500g/mとすることが好ましい。150g/m以下であると、紙容器に成型した際に剛性が不足するおそれがある。また500g/m2以上であると、薬品、原料を多量に使用するためコスト高となるおそれがある。 The basis weight of the paper substrate is not particularly limited, but is preferably 150 to 500 g/m 2 . If it is 150 g/m 2 or less, the rigidity may be insufficient when molded into a paper container. On the other hand, when it is 500 g/m 2 or more, a large amount of chemicals and raw materials are used, which may result in high cost.

紙基材の少なくとも一方の面上に、水溶性高分子の層や、顔料及び接着剤を主成分とする塗工層を設けてもよい。これらの層は単独、または2種以上を組み合わせて使用することができる。水溶性高分子層や塗工層を設けることによって、直鎖脂肪酸や直鎖アルコールのブリーディングの程度を調整することが可能となる。水溶性高分子としては特に限定されないが、加工適性の観点から、ポリビニルアルコール(PVA)、澱粉類、ポリアクリルアミド類、ポリエチレンイミン類等が好ましい。塗工層に用いることのできる顔料は、特に限定されるものではなく、例えば、各種カオリン、タルク、若しくは重質炭酸カルシウムなどの精製した天然鉱物顔料、軽質炭酸カルシウム、若しくは炭酸カルシウムと他の親水性有機化合物との複合合成顔料、サチンホワイト、リトポン、二酸化チタン、シリカ、アルミナ、水酸化アルミニウム、酸化亜鉛、炭酸マグネシウム、焼成カオリン、中空有機顔料、密実有機顔料、プラスチックピグメント、バインダーピグメント、プラスチックビーズ、又はマイクロカプセル等があるが、これらに限定されるものではない。水溶性高分子層や、塗工層の形成方法については特に制限されず、ブレードコーター、ロッドコーター等を用いることができる。 A water-soluble polymer layer or a coating layer containing a pigment and an adhesive as a main component may be provided on at least one surface of the paper substrate. These layers can be used alone or in combination of two or more kinds. By providing the water-soluble polymer layer or the coating layer, the degree of bleeding of the linear fatty acid or the linear alcohol can be adjusted. The water-soluble polymer is not particularly limited, but from the viewpoint of processability, polyvinyl alcohol (PVA), starches, polyacrylamides, polyethyleneimines and the like are preferable. The pigment that can be used for the coating layer is not particularly limited, and examples thereof include purified natural mineral pigments such as various kaolin, talc, or ground calcium carbonate, light calcium carbonate, or calcium carbonate and other hydrophilic materials. Composite pigments with organic compounds, satin white, lithopone, titanium dioxide, silica, alumina, aluminum hydroxide, zinc oxide, magnesium carbonate, calcined kaolin, hollow organic pigments, solid organic pigments, plastic pigments, binder pigments, plastics Examples thereof include beads, microcapsules, and the like, but are not limited to these. The method for forming the water-soluble polymer layer and the coating layer is not particularly limited, and a blade coater, a rod coater or the like can be used.

(抄紙)
紙基材は、抄紙工程で抄紙して製造される。紙基材の抄紙方法および抄紙機の型式としては、長網抄紙機、ツインワイヤー抄紙機、円網抄紙機、ギャップフォーマー、オントップフォーマー、サクセスフォーマー等の公知の抄紙方法および抄紙機を用いることができ、限定されない。特に、多層紙を抄紙する時は、多層抄き用抄紙機を用いることが好ましい。また、抄紙時のpHは酸性領域(酸性抄紙)、疑似中性領域(疑似中性抄紙)、中性領域(中性抄紙)、アルカリ性領域(アルカリ性抄紙)のいずれであってもよく、限定されない。
(Papermaking)
The paper base material is manufactured by making paper in the paper making process. The paper-making method of paper base material and the type of paper-making machine include known paper-making methods and paper-making machines such as fourdrinier paper machine, twin wire paper machine, cylinder paper machine, gap former, on-top former, success former and the like. Can be used and is not limited. In particular, when making multi-layer paper, it is preferable to use a multi-layer paper machine. The pH during papermaking may be any of acidic region (acidic papermaking), pseudo-neutral region (pseudo-neutral papermaking), neutral region (neutral papermaking), and alkaline region (alkaline papermaking), and is not limited. ..

[熱可塑性樹脂層]
熱可塑性樹脂層は、紙基材上に熱可塑性樹脂層をラミネートすることによって形成される。熱可塑性樹脂は、用途に応じて、結晶性樹脂と非結晶性樹脂のいずれの熱可塑性樹脂も使用できる。熱可塑性樹脂としては、ポリエチレン(LDPE、MDPE、HDPE、LLDPE等)、ポリプロピレン、ポリメチルペンテン等のポリオレフィン樹脂、PET、PBT等のポリエステル樹脂、ポリアミド樹脂、ポリ乳酸、PHB、PBS、PBAT、PCL、PHBH等の生分解性樹脂、ポリスチレン、ポリ塩化ビニル、アクリロニトリル・ブタジエン・スチレン(ABS)樹脂、アクリル樹脂、変性ポリフェニレンエーテル(PPE)等が挙げられる。
[Thermoplastic resin layer]
The thermoplastic resin layer is formed by laminating the thermoplastic resin layer on a paper base material. As the thermoplastic resin, either a crystalline resin or a non-crystalline resin can be used depending on the application. As the thermoplastic resin, polyethylene (LDPE, MDPE, HDPE, LLDPE, etc.), polypropylene, polyolefin resin such as polymethylpentene, polyester resin such as PET and PBT, polyamide resin, polylactic acid, PHB, PBS, PBAT, PCL, Examples thereof include biodegradable resins such as PHBH, polystyrene, polyvinyl chloride, acrylonitrile butadiene styrene (ABS) resin, acrylic resin, and modified polyphenylene ether (PPE).

熱可塑性樹脂層は、単一の樹脂の単層で形成してもよいし、複数の樹脂を混合して単層で形成してもよいし、同種や異種の樹脂からなる複数の層として形成してもよい。 The thermoplastic resin layer may be formed as a single layer of a single resin, may be formed as a single layer by mixing a plurality of resins, or may be formed as a plurality of layers of the same kind or different kinds of resins. You may.

熱可塑性樹脂層の厚さは、特に限定されないが、通常は、10〜50μm程度の厚さである。 The thickness of the thermoplastic resin layer is not particularly limited, but is usually about 10 to 50 μm.

[ラミネート紙]
ラミネート紙は、紙基材と、当該紙基材の少なくとも一方の面上に積層された熱可塑性樹脂層とからなる。熱可塑性樹脂層は、紙基材の片面だけに積層されていてもよいし、紙基材の両面に積層されていてもよい。ラミネート紙は、紙基材の少なくとも一方の面上に熱可塑性樹脂層を積層するラミネート工程で積層されて製造される。
[Laminated paper]
The laminated paper includes a paper base material and a thermoplastic resin layer laminated on at least one surface of the paper base material. The thermoplastic resin layer may be laminated only on one side of the paper base material, or may be laminated on both sides of the paper base material. Laminated paper is manufactured by laminating a thermoplastic resin layer on at least one surface of a paper base material in a laminating step.

熱可塑性樹脂層を紙基材上にラミネートする方法としては、押出ラミネート法、ドライラミネート法、ウェットラミネート法、熱ラミネート法、共押出ラミネート等の各種公知の方法を適宜使用することができる。 As a method for laminating the thermoplastic resin layer on the paper substrate, various known methods such as extrusion laminating method, dry laminating method, wet laminating method, thermal laminating method, and coextrusion laminating method can be appropriately used.

ラミネート時には、必要に応じて、紙基材または熱可塑性樹脂層に対してコロナ処理やオゾン処理等の酸化処理を施してもよい。これらの処理を行うことによって、紙基材または熱可塑性樹脂層の表面に極性基が生成し、接着性を向上させることができる。これら処理は紙基材または熱可塑性樹脂層のいずれか一方に行ってもよく、両方に行ってもよい。またこれら処理回数は1度であってもよいし、複数回を繰り返してもよい。 When laminating, the paper base material or the thermoplastic resin layer may be subjected to an oxidation treatment such as corona treatment or ozone treatment, if necessary. By performing these treatments, polar groups are generated on the surface of the paper base material or the thermoplastic resin layer, and the adhesiveness can be improved. These treatments may be performed on either the paper substrate or the thermoplastic resin layer, or both. Further, the number of times of these processes may be once or may be repeated a plurality of times.

ラミネート紙の製造時において、抄紙工程およびラミネート工程の少なくともいずれかの工程で、紙基材に100℃以上に加熱された物を接触させる。紙基材に100℃以上に加熱された物を接触させることによって、紙基材の内部に含有されている直鎖脂肪酸および直鎖アルコールが溶けて、それらを紙基材内に均一に分布させることができる。100℃以上に加熱された物は、例えばドライヤー、加熱ロール、加熱シリンダーロール、押出機、赤外線ヒーター等の装置であっても、ラミネート時の熱可塑性樹脂であってもよく、特に限定されない。また、加熱された物と接触させる方法も、直接的に接触させてもよいし、カンバス、空気等を通じて間接的に接触させてもよい。これらの処理回数は1回であってもよいし、複数回繰り返してもよい。 At the time of manufacturing a laminated paper, a material heated to 100° C. or higher is brought into contact with a paper base material in at least one of a papermaking step and a laminating step. By contacting a material heated to 100° C. or higher with the paper base material, the linear fatty acid and the linear alcohol contained inside the paper base material are dissolved, and they are evenly distributed in the paper base material. be able to. The material heated to 100° C. or higher may be a device such as a dryer, a heating roll, a heating cylinder roll, an extruder, an infrared heater, or a thermoplastic resin at the time of lamination, and is not particularly limited. Also, the method of contacting with a heated object may be direct contact, or indirect contact through canvas, air or the like. These treatments may be performed once or may be repeated a plurality of times.

紙基材と熱可塑性樹脂層とからなるラミネート紙は、坪量が150〜500g/mであることが好ましく、200〜400g/mであることがより好ましい。坪量が小さ過ぎると、ラミネート紙の製造時に熱が伝わり過ぎるため、直鎖脂肪酸や直鎖アルコールが製造時に過剰にブリーディングしてしまうおそれがある。一方、坪量が大き過ぎると、ラミネート紙の製造時に熱が伝わり難いため、直鎖脂肪酸や直鎖アルコールが製造時に均一に分散することができず、ブリーディングが均一に起こらず、剥離しにくくなるおそれがある。 The laminated paper composed of the paper base material and the thermoplastic resin layer preferably has a basis weight of 150 to 500 g/m 2 , and more preferably 200 to 400 g/m 2 . If the basis weight is too small, heat will be transferred too much during the production of the laminated paper, which may cause excessive bleeding of the linear fatty acid or the linear alcohol during the production. On the other hand, if the basis weight is too large, heat is difficult to transfer during the production of the laminated paper, so that the straight-chain fatty acid or the straight-chain alcohol cannot be uniformly dispersed during the production, and bleeding does not occur uniformly, and peeling becomes difficult. There is a risk.

紙基材と熱可塑性樹脂層とからなるラミネート紙は、厚さが200〜750μmであることが好ましい。また、紙基材と熱可塑性樹脂層とからなるラミネート紙は、密度が0.50〜1.30g/cmであることが好ましく、0.60〜1.20g/cmであることがさらに好ましい。 The laminated paper including the paper base material and the thermoplastic resin layer preferably has a thickness of 200 to 750 μm. Further, laminated paper comprising a paper substrate and the thermoplastic resin layer is preferably a density of 0.50~1.30g / cm 3, to be 0.60~1.20g / cm 3 further preferable.

本実施形態のラミネート紙は、ラミネート紙の製造時から容器として使用する時までは、十分なラミネートの接着性を有している。しかし、容器を使用後に回収し、再利用する頃には、接着性が低下して、紙基材と熱可塑性樹脂層とが剥離し易くなるため、紙基材のパルプを容易にリサイクルすることができる。 The laminated paper of the present embodiment has sufficient laminate adhesiveness from the time of manufacturing the laminated paper to the time of using it as a container. However, when the container is collected after use and reused, the adhesiveness deteriorates and the paper base material and the thermoplastic resin layer are easily separated, so that the pulp of the paper base material should be easily recycled. You can

一般に、ラミネート紙をパルプ繊維が主体の紙基材と熱可塑性樹脂層とに分離するリサイクル工程において、ラミネート紙はパルパーに投入され離解が行われる。本実施形態のラミネート紙では、紙基材と熱可塑性樹脂層とが剥離し易くなるため、原料を容易に分離することができ、回収リサイクルすることができる。 Generally, in a recycling process in which laminated paper is separated into a paper base material mainly composed of pulp fibers and a thermoplastic resin layer, the laminated paper is put into a pulper and disaggregated. In the laminated paper of the present embodiment, the paper base material and the thermoplastic resin layer are easily separated from each other, so that the raw materials can be easily separated and can be collected and recycled.

ラミネート紙の層構成としては、紙基材と熱可塑性樹脂層とからなる2層構成または3層構成のラミネート紙が基本であるが、それ以外に、用途に応じて、種々の多様な層構成を形成することができる。例えば、紙基材と熱可塑性樹脂層とからなるラミネート紙上にさらに同種または異種の熱可塑性樹脂層を設けたり、熱可塑性樹脂層と熱可塑性樹脂層の間に熱可塑性樹脂層以外の層を設けたり、紙基材と熱可塑性樹脂層の間に熱可塑性樹脂層以外の層を設けることもできる。熱可塑性樹脂層以外の層としては、上記の水溶性高分子層(PVA等)や、顔料及び接着剤を主成分とする塗工層、アルミニウム箔(Al箔)、印刷層等がある。 The laminated paper is basically a laminated paper having a two-layer structure or a three-layer structure composed of a paper base material and a thermoplastic resin layer. Can be formed. For example, a thermoplastic resin layer of the same type or different types may be further provided on a laminated paper composed of a paper base material and a thermoplastic resin layer, or a layer other than the thermoplastic resin layer may be provided between the thermoplastic resin layer and the thermoplastic resin layer. Alternatively, a layer other than the thermoplastic resin layer may be provided between the paper base material and the thermoplastic resin layer. Layers other than the thermoplastic resin layer include the above-mentioned water-soluble polymer layer (PVA or the like), a coating layer containing a pigment and an adhesive as a main component, an aluminum foil (Al foil), a printing layer and the like.

具体的なラミネート紙の層構成の例としては、紙基材/LDPE、紙基材/塗工層/LDPE、LDPE/紙基材/LDPE、LDPE/紙基材/塗工層/LDPE、LDPE/PVA/紙基材/PVA/LDPE、LDPE/紙基材/LDPE/PET/LDPE、LDPE/紙基材/LDPE/Al箔/LDPE等があるが、これらに限定されない。 Specific examples of the layer structure of laminated paper include paper base/LDPE, paper base/coating layer/LDPE, LDPE/paper base/LDPE, LDPE/paper base/coating layer/LDPE, LDPE. /PVA/paper base material/PVA/LDPE, LDPE/paper base material/LDPE/PET/LDPE, LDPE/paper base material/LDPE/Al foil/LDPE, but not limited to these.

[紙容器]
本実施形態のラミネート紙を用いて種々の紙容器を製造することができる。紙容器を製造する方法は、公知の方法を適宜選択して用いることができる。
[Paper container]
Various paper containers can be manufactured using the laminated paper of this embodiment. As a method of manufacturing the paper container, a known method can be appropriately selected and used.

[液体用紙容器]
本実施形態のラミネート紙を用いて種々の液体用紙容器を製造することができる。液体用紙容器を製造する方法は、公知の方法を適宜選択して用いることができる。
[Liquid paper container]
Various liquid paper containers can be manufactured using the laminated paper of this embodiment. As a method of manufacturing the liquid paper container, a known method can be appropriately selected and used.

熱可塑性樹脂層が内側となるように紙容器を製造することによって、内容物の液体は、熱可塑性樹脂層によって保持されるため、紙基材側に液体が浸透して、紙基材が変色したり、劣化したりするのを抑制することができる。 By manufacturing the paper container so that the thermoplastic resin layer is on the inside, the liquid of the contents is held by the thermoplastic resin layer, so the liquid penetrates into the paper base material side and the paper base material discolors. And deterioration can be suppressed.

PE等の熱可塑性樹脂層を紙基材の外側および内側の両面に設けたラミネート紙を、水の沸点及び熱可塑性樹脂の融点を超える温度で加熱処理して、当該熱可塑性樹脂層を紙基材が含有する水分等によって発泡させると、断熱性を有した紙容器とすることができる。断熱性を有する紙容器は、例えば、加熱した液体・固体等や冷却された液体・固体等を内容物とする断熱性紙容器として使用することができる。 Laminated paper provided with a thermoplastic resin layer such as PE on both the outside and the inside of a paper substrate is heat-treated at a temperature higher than the boiling point of water and the melting point of the thermoplastic resin to form the thermoplastic resin layer on the paper base. By foaming with the water content of the material, a paper container having a heat insulating property can be obtained. The heat-insulating paper container can be used as, for example, a heat-insulating paper container whose contents are a heated liquid/solid or a cooled liquid/solid.

本実施形態のラミネート紙は、牛乳パック等の液体用紙容器、紙コップ、発泡カップ、アイスカップ、断熱カップ、コーヒー容器、アセプティック容器、包装容器等の紙容器のほか、包装資材、断熱資材等の各種用途に用いることができる。 The laminated paper of this embodiment is a liquid paper container such as a milk carton, a paper cup, a foaming cup, an ice cup, a heat insulating cup, a coffee container, an aseptic container, a paper container such as a packaging container, and a variety of packaging materials, heat insulating materials, and the like. It can be used for various purposes.

以下、実施例により本発明の効果を詳細に説明する。実施例および比較例中の「部」および「%」は、特に断らない限り、それぞれ「質量部」および「質量%」を示す。 Hereinafter, the effects of the present invention will be described in detail with reference to Examples. Unless otherwise specified, "parts" and "%" in Examples and Comparative Examples represent "parts by mass" and "% by mass", respectively.

実施例および比較例に用いた材料は以下のとおりである。
(1)パルプ
LBKP:アカシアパルプ、ユーカリパルプ
NBKP:ダグラスファー、ラジアータパイン、スギ
(2)熱可塑性樹脂
PE:日本ポリエチレン社製LDPE、品番LC522
The materials used in Examples and Comparative Examples are as follows.
(1) Pulp LBKP: Acacia pulp, eucalyptus pulp NBKP: Douglas fir, radiata pine, cedar (2) Thermoplastic resin PE: LDPE manufactured by Nippon Polyethylene Co., product number LC522

以下に、紙基材およびラミネート紙について実施した測定方法を示す。なお特別な記載が無い限り、測定はJIS P8111:1998に記載の温度23℃±1℃、湿度50±2%の環境で行った。 Below, the measuring method implemented about the paper base material and laminated paper is shown. Unless otherwise specified, the measurement was performed in an environment of a temperature of 23° C.±1° C. and a humidity of 50±2% described in JIS P8111:1998.

(1)繊維形態は、JIS P8226:2006に従い、投影長さ加重平均繊維長と粗度を測定した。測定には繊維長測定装置 (メッツォオートメーション社製、カヤーニファイバーラボVer4.0)を用いた。
(2)坪量:JIS P8124:2011に準じて測定した。
(3)厚さ:JIS P8118:2014に従い、100kPa±10kPaの圧力を試験片の円形領域(200mm)に加えた際の厚さを測定した。
(4)密度:JIS P8118:2014に従い測定した。なお厚さは、100kPa±10kPaの圧力を試験片の円形領域(200mm)に加えた際の厚さを測定した。
(5)水分:JIS P8127:2010に従い測定した。
(1) For the fiber morphology, the projected length weighted average fiber length and the roughness were measured according to JIS P8226:2006. A fiber length measuring device (manufactured by Metso Automation Co., Ltd., Kajaani Fiber Lab Ver4.0) was used for the measurement.
(2) Basis weight: Measured according to JIS P8124:2011.
(3) Thickness: According to JIS P8118:2014, the thickness when a pressure of 100 kPa±10 kPa was applied to the circular region (200 mm 2 ) of the test piece was measured.
(4) Density: Measured according to JIS P8118:2014. The thickness was measured when a pressure of 100 kPa±10 kPa was applied to the circular region (200 mm 2 ) of the test piece.
(5) Water content: Measured according to JIS P8127:2010.

直鎖脂肪酸および直鎖アルコールの含有量の測定は以下のように行った。
紙基材30mm×30mmを切り出し、精量した。切り出した試験片を厚さ方向に層剥離した後、その全量を10mm×10mmの小断片に分割した。分割した試験片の全てをガラス容器に入れ、濃塩酸(12規定)0.1ml、及びクロロホルム2ml加え、30分間超音波処理を行った。このとき得られた抽出液をメンブレンフィルタ(ポア径0.2μm)で濾過した。上記濾液を用いて高速液体クロマトグラフィーにより分析を行った。溶離液としてメタノール:トリフルオロ酢酸を0.1%含んだアセトン=50:50を用い、流量1ml/分とした。使用カラムはウォーターズ社製X Bridge C18, 250mm×4.6mm I.Dで、温度は30℃とし、濾液を2μl注入した。検出器は荷電化粒子検出器を用いて、直鎖アルコール及び直鎖脂肪酸を検出し、それぞれについて下記の計算式により試料中濃度を求め、合計を算出した。各成分のピーク面積値は、ベーズラインと各ピークで囲まれた部分であるが、部分的に重複するピークについてはJIS K 0124の垂線法によりピーク分離し求めた。
計算式:試料中濃度(ppm)={標品濃度÷標品ピーク面積値}×試料ピーク面積値×2(ml)÷{(試料質量(mg)÷1000)}
The linear fatty acid and linear alcohol contents were measured as follows.
A 30 mm×30 mm paper substrate was cut out and weighed precisely. After delaminating the cut-out test piece in the thickness direction, the total amount was divided into 10 mm×10 mm small pieces. All of the divided test pieces were placed in a glass container, 0.1 ml of concentrated hydrochloric acid (12N) and 2 ml of chloroform were added, and ultrasonic treatment was performed for 30 minutes. The extract obtained at this time was filtered with a membrane filter (pore diameter 0.2 μm). The filtrate was analyzed by high performance liquid chromatography. As an eluent, acetone=50:50 containing 0.1% of methanol:trifluoroacetic acid was used, and the flow rate was 1 ml/min. The column used was a Waters X Bridge C18, 250 mm×4.6 mm I.D. In D, the temperature was 30° C. and 2 μl of the filtrate was injected. The detector used a charged particle detector to detect linear alcohols and linear fatty acids, and for each of them, the concentration in the sample was determined by the following calculation formula, and the total was calculated. The peak area value of each component is the portion surrounded by the baze line and each peak, but peaks that partially overlap were determined by peak separation according to the perpendicular method of JIS K 0124.
Calculation formula: Concentration in sample (ppm)={standard sample concentration/standard sample peak area value}×sample peak area value×2 (ml)÷{(sample mass (mg)÷1000)}

[実施例1]
(紙基材)
パルプ原料としてLBKP100部(アカシア材80%、ユーカリ材20%)を、ダブルディスクレファイナーを使用して叩解し、パルプスラリーを得た。得られたパルプスラリー100部に対して、内添紙力増強剤としてカチオン化澱粉0.60部(固形分換算)、内添サイズ剤としてアルキルケテンダイマー系サイズ剤0.30部(固形分換算)、硫酸バンドを0.20部(固形分換算)、湿潤紙力剤として、ポリアミド・アミンエピクロロヒドリン系湿潤紙力剤を0.10質量部(固形分換算)を添加し紙料を調製した。この紙料を用いて5層抄きの長網抄紙機を用いて抄紙した。抄紙工程中、層間スプレーにて、各層間にバレイショ澱粉を3.0質量部(固形分換算)吹き付けるとともに、5層抄き合わせ後に、紙基材の表面にサイズプレスで酸化澱粉を1.0g/m(固形分換算)塗布し、坪量274g/mの紙基材を得た。得られた紙基材には、表1に記載の直鎖脂肪酸および直鎖アルコールが含まれていた。
[Example 1]
(Paper substrate)
As a pulp raw material, 100 parts of LBKP (80% acacia wood, 20% eucalyptus wood) was beaten using a double disc refiner to obtain a pulp slurry. With respect to 100 parts of the obtained pulp slurry, 0.60 parts of cationic starch (solid content conversion) as an internal paper strength enhancer and 0.30 part of alkyl ketene dimer sizing agent as solid addition size agent (solid content conversion) ), 0.20 part of sulfuric acid band (solid content conversion), and 0.10 parts by mass (solid content conversion) of a polyamide-amine epichlorohydrin-based wet paper strength agent as a wet paper strength agent. Prepared. Using this stock, a five-layer fourdrinier paper machine was used to make paper. During the papermaking process, 3.0 parts by mass (in terms of solid content) of potato starch was sprayed between the layers by interlayer spraying, and after 5 layers of papermaking, 1.0 g of oxidized starch was applied to the surface of the paper base material by a size press. /M 2 (solid content conversion) was applied to obtain a paper base material having a basis weight of 274 g/m 2 . The obtained paper substrate contained the linear fatty acid and linear alcohol shown in Table 1.

(熱可塑性樹脂層)
得られた紙基材の外内両面に対し、熱可塑性樹脂としてLDPE(LC522)をラミネートした。熱可塑性樹脂層のラミネートは押し出しラミネート法により、ラミネート温度を330℃、ラミネート速度を200m/分の条件で行った。熱可塑性樹脂層の厚さ、質量は表1に記載の通りとし、ラミネート紙を得た。
(Thermoplastic resin layer)
LDPE (LC522) as a thermoplastic resin was laminated on both the outer and inner surfaces of the obtained paper substrate. The lamination of the thermoplastic resin layer was performed by an extrusion laminating method at a laminating temperature of 330° C. and a laminating speed of 200 m/min. The thickness and mass of the thermoplastic resin layer were as described in Table 1, and laminated paper was obtained.

(紙容器)
得られたラミネート紙の表面にオフセット印刷を施したのち、必要箇所に罫線を設け、所定の形状に打ち抜き、ブランク材を得た。次に、フレームシールによりブランク材の一部の樹脂材料を溶融し、胴部を貼り合わせて、筒状のスリーブを得た。続いて、この筒状スリーブを液体充填機に供給し、充填機上でボトム部を形成した後、トップ部をシールし、ゲーブルトップ型紙容器を得た。
(Paper container)
After offset printing was performed on the surface of the obtained laminated paper, ruled lines were provided at necessary positions and punched into a predetermined shape to obtain a blank material. Next, a part of the resin material of the blank material was melted by frame sealing, and the body portion was bonded to obtain a cylindrical sleeve. Subsequently, this tubular sleeve was supplied to a liquid filling machine to form a bottom portion on the filling machine, and then the top portion was sealed to obtain a gable top type paper container.

[実施例2]
パルプ原料としてLBKP100部(アカシア材70%、ユーカリ材30%)を、ダブルディスクレファイナーを使用して叩解し、パルプスラリーを得た。得られたパルプスラリー100部に対して、内添紙力増強剤としてカチオン化澱粉0.60部(固形分換算)、内添サイズ剤としてアルキルケテンダイマー系サイズ剤0.30部(固形分換算)、硫酸バンドを0.20部(固形分換算)、湿潤紙力剤として、ポリアミド・アミンエピクロロヒドリン系湿潤紙力剤を0.10質量部(固形分換算)を添加し紙料を調製した。この紙料を用いて5層抄きの長網抄紙機を用いて抄紙した。抄紙工程中、層間スプレーにて、各層間にバレイショ澱粉を3.0質量部(固形分換算)吹き付けるとともに、5層抄き合わせ後に、紙基材の表面にサイズプレスで酸化澱粉を1.0g/m(固形分換算)塗布し、坪量476g/mの紙基材を得た。得られた紙基材には、表1に記載の直鎖脂肪酸および直鎖アルコールが含まれていた。
得られた紙基材に、厚さ、質量を表1に記載の条件となるよう熱可塑性樹脂層をラミネートした以外は実施例1と同様にして、ゲーブルトップ型紙容器を得た。
[Example 2]
As a pulp raw material, 100 parts of LBKP (acacia wood 70%, eucalyptus wood 30%) was beaten using a double disc refiner to obtain a pulp slurry. With respect to 100 parts of the obtained pulp slurry, 0.60 parts of cationic starch (solid content conversion) as an internal paper strength enhancer and 0.30 part of alkyl ketene dimer sizing agent as solid addition size agent (solid content conversion) ), 0.20 part of sulfuric acid band (solid content conversion), and 0.10 parts by mass (solid content conversion) of a polyamide-amine epichlorohydrin-based wet paper strength agent as a wet paper strength agent. Prepared. Using this stock, a five-layer fourdrinier paper machine was used to make paper. During the papermaking process, 3.0 parts by mass (in terms of solid content) of potato starch was sprayed between the layers by interlayer spraying, and after 5 layers of papermaking, 1.0 g of oxidized starch was applied to the surface of the paper base material by a size press. /M 2 (solid content conversion) was applied to obtain a paper base material having a basis weight of 476 g/m 2 . The obtained paper substrate contained the linear fatty acid and linear alcohol shown in Table 1.
A gable-top type paper container was obtained in the same manner as in Example 1 except that the thermoplastic resin layer was laminated on the obtained paper base material so that the thickness and the weight were as shown in Table 1.

[実施例3]
パルプ原料としてLBKP80部(アカシア材60%、ユーカリ材40%)、NBKP20部(ダグラスファー50%、ラジアータパイン30%、スギ20%)を、それぞれダブルディスクレファイナーを使用して叩解し、パルプスラリーを得た。得られたパルプスラリー100部に対して、内添紙力増強剤としてカチオン化澱粉0.60部(固形分換算)、内添サイズ剤としてアルキルケテンダイマー系サイズ剤0.30部(固形分換算)、硫酸バンドを0.20部(固形分換算)、湿潤紙力剤として、ポリアミド・アミンエピクロロヒドリン系湿潤紙力剤を0.10質量部(固形分換算)を添加し紙料を調製した。この紙料を用いて5層抄きの長網抄紙機を用いて抄紙した。抄紙工程中、層間スプレーにて、各層間にバレイショ澱粉を3.0質量部(固形分換算)吹き付けるとともに、5層抄き合わせ後に、紙基材の表面にサイズプレスで酸化澱粉を3.0g/m(固形分換算)塗布し、坪量152g/mの紙基材を得た。得られた紙基材には、表1に記載の直鎖脂肪酸および直鎖アルコールが含まれていた。
得られた紙基材に、厚さ、質量を表1に記載の条件となるよう熱可塑性樹脂層をラミネートした以外は実施例1と同様にして、ゲーブルトップ型紙容器を得た。
[Example 3]
80 parts of LBKP (60% of acacia wood, 40% of eucalyptus wood) and 20 parts of NBKP (50% of Douglas fir, 30% of radiata pine, 20% of cedar) as pulp raw materials were beaten using a double disc refiner, respectively, to obtain a pulp slurry. Got With respect to 100 parts of the obtained pulp slurry, 0.60 parts of cationic starch (solid content conversion) as an internal paper strength enhancer and 0.30 part of alkyl ketene dimer sizing agent as solid addition size agent (solid content conversion) ), 0.20 part of sulfuric acid band (solid content conversion), and 0.10 parts by mass (solid content conversion) of a polyamide-amine epichlorohydrin-based wet paper strength agent as a wet paper strength agent. Prepared. Using this stock, a five-layer fourdrinier paper machine was used to make paper. During the papermaking process, 3.0 parts by mass (in terms of solid content) of potato starch was sprayed between the layers by interlayer spraying, and after 5 layers of papermaking, 3.0 g of oxidized starch was applied to the surface of the paper substrate with a size press. /M 2 (solid content conversion) was applied to obtain a paper base material having a basis weight of 152 g/m 2 . The obtained paper substrate contained the linear fatty acid and linear alcohol shown in Table 1.
A gable-top type paper container was obtained in the same manner as in Example 1 except that the thermoplastic resin layer was laminated on the obtained paper base material so that the thickness and the weight were as shown in Table 1.

[実施例4]
パルプ原料としてLBKP80部(アカシア材40%、ユーカリ材60%)、NBKP20部(ダグラスファー50%、ラジアータパイン30%、スギ20%)を、それぞれダブルディスクレファイナーを使用して叩解し、パルプスラリーを得た。得られたパルプスラリー100部に対して、内添紙力増強剤としてカチオン化澱粉0.60部(固形分換算)、内添サイズ剤としてアルキルケテンダイマー系サイズ剤0.30部(固形分換算)、硫酸バンドを0.20部(固形分換算)、湿潤紙力剤として、ポリアミド・アミンエピクロロヒドリン系湿潤紙力剤を0.10質量部(固形分換算)を添加し紙料を調製した。この紙料を用いて5層抄きの長網抄紙機を用いて抄紙した。抄紙工程中、層間スプレーにて、各層間にバレイショ澱粉を4.0質量部(固形分換算)吹き付けるとともに、5層抄き合わせ後に、紙基材の表面にサイズプレスで酸化澱粉を3.0g/m(固形分換算)塗布し、坪量370g/mの紙基材を得た。得られた紙基材には、表1に記載の直鎖脂肪酸および直鎖アルコールが含まれていた。
得られた紙基材に、厚さ、質量を表1に記載の条件となるよう熱可塑性樹脂層をラミネートした以外は実施例1と同様にして、ゲーブルトップ型紙容器を得た。
[Example 4]
As a pulp raw material, 80 parts of LBKP (40% of acacia wood, 60% of eucalyptus wood) and 20 parts of NBKP (50% of Douglas fir, 30% of radiata pine, 20% of cedar) were beaten using a double disc refiner, respectively, to obtain a pulp slurry. Got With respect to 100 parts of the obtained pulp slurry, 0.60 parts of cationic starch (solid content conversion) as an internal paper strength enhancer and 0.30 part of alkyl ketene dimer sizing agent as solid addition size agent (solid content conversion) ), 0.20 part of sulfuric acid band (solid content conversion), and 0.10 parts by mass (solid content conversion) of a polyamide-amine epichlorohydrin-based wet paper strength agent as a wet paper strength agent. Prepared. Using this stock, a five-layer fourdrinier paper machine was used to make paper. During the papermaking process, 4.0 parts by mass (in terms of solid content) of potato starch was sprayed between the layers by interlayer spraying, and after 5 layers of papermaking, 3.0 g of oxidized starch was applied to the surface of the paper substrate with a size press. /M 2 (solid content conversion) was applied to obtain a paper base material having a basis weight of 370 g/m 2 . The obtained paper substrate contained the linear fatty acid and linear alcohol shown in Table 1.
A gable-top type paper container was obtained in the same manner as in Example 1 except that the thermoplastic resin layer was laminated on the obtained paper base material so that the thickness and the weight were as shown in Table 1.

[実施例5]
パルプ原料としてLBKP50部(アカシア材50%、ユーカリ材50%)、NBKP50部(ダグラスファー50%、ラジアータパイン30%、スギ20%)を、それぞれダブルディスクレファイナーを使用して叩解し、パルプスラリーを得た。得られたパルプスラリー100部に対して、内添紙力増強剤としてカチオン化澱粉0.60部(固形分換算)、内添サイズ剤としてアルキルケテンダイマー系サイズ剤0.30部(固形分換算)、硫酸バンドを0.20部(固形分換算)、湿潤紙力剤として、ポリアミド・アミンエピクロロヒドリン系湿潤紙力剤を0.10質量部(固形分換算)を添加し紙料を調製した。この紙料を用いて5層抄きの長網抄紙機を用いて抄紙した。抄紙工程中、層間スプレーにて、各層間にバレイショ澱粉を4.0質量部(固形分換算)吹き付けるとともに、5層抄き合わせ後に、紙基材の表面にサイズプレスで酸化澱粉を3.0g/m(固形分換算)塗布し、坪量226g/mの紙基材を得た。得られた紙基材には、表1に記載の直鎖脂肪酸および直鎖アルコールが含まれていた。
得られた紙基材に、厚さ、質量を表1に記載の条件となるよう熱可塑性樹脂層をラミネートした以外は実施例1と同様にして、ゲーブルトップ型紙容器を得た。
[Example 5]
50 parts of LBKP (50% of acacia wood, 50% of eucalyptus wood) and 50 parts of NBKP (50% of Douglas fir, 30% of radiata pine, 20% of cedar) as pulp raw materials were beaten using a double disc refiner, respectively, to obtain a pulp slurry. Got With respect to 100 parts of the obtained pulp slurry, 0.60 parts of cationic starch (solid content conversion) as an internal paper strength enhancer and 0.30 part of alkyl ketene dimer sizing agent as solid addition size agent (solid content conversion) ), 0.20 part of sulfuric acid band (solid content conversion), and 0.10 parts by mass (solid content conversion) of a polyamide-amine epichlorohydrin-based wet paper strength agent as a wet paper strength agent. Prepared. Using this stock, a five-layer fourdrinier paper machine was used to make paper. During the papermaking process, 4.0 parts by mass (in terms of solid content) of potato starch was sprayed between the layers by interlayer spraying, and after 5 layers of papermaking, 3.0 g of oxidized starch was applied to the surface of the paper substrate with a size press. /M 2 (solid content conversion) was applied to obtain a paper base material having a basis weight of 226 g/m 2 . The obtained paper substrate contained the linear fatty acid and linear alcohol shown in Table 1.
A gable-top type paper container was obtained in the same manner as in Example 1 except that the thermoplastic resin layer was laminated on the obtained paper base material so that the thickness and the weight were as shown in Table 1.

[実施例6]
パルプ原料としてLBKP50部(アカシア材50%、ユーカリ材50%)、NBKP50部(ダグラスファー50%、ラジアータパイン30%、スギ20%)を、それぞれダブルディスクレファイナーを使用して叩解し、パルプスラリーを得た。得られたパルプスラリー100部に対して、内添紙力増強剤としてカチオン化澱粉0.60部(固形分換算)、内添サイズ剤としてアルキルケテンダイマー系サイズ剤0.30部(固形分換算)、硫酸バンドを0.20部(固形分換算)、湿潤紙力剤として、ポリアミド・アミンエピクロロヒドリン系湿潤紙力剤を0.10質量部(固形分換算)を添加し紙料を調製した。この紙料を用いて5層抄きの長網抄紙機を用いて抄紙した。抄紙工程中、層間スプレーにて、各層間にバレイショ澱粉を4.0質量部(固形分換算)吹き付けるとともに、5層抄き合わせ後に、紙基材の表面にサイズプレスで酸化澱粉を4.0g/m(固形分換算)塗布し、坪量374g/mの紙基材を得た。得られた紙基材には、表1に記載の直鎖脂肪酸および直鎖アルコールが含まれていた。
得られた紙基材に、厚さ、質量を表1に記載の条件となるよう熱可塑性樹脂層をラミネートした以外は実施例1と同様にして、ゲーブルトップ型紙容器を得た。
[Example 6]
50 parts of LBKP (50% of acacia wood, 50% of eucalyptus wood) and 50 parts of NBKP (50% of Douglas fir, 30% of radiata pine, 20% of cedar) as pulp raw materials were beaten using a double disc refiner, respectively, to obtain a pulp slurry. Got With respect to 100 parts of the obtained pulp slurry, 0.60 parts of cationic starch (solid content conversion) as an internal paper strength enhancer and 0.30 part of alkyl ketene dimer sizing agent as solid addition size agent (solid content conversion) ), 0.20 part of sulfuric acid band (solid content conversion), and 0.10 parts by mass (solid content conversion) of a polyamide-amine epichlorohydrin-based wet paper strength agent as a wet paper strength agent. Prepared. Using this stock, a five-layer fourdrinier paper machine was used to make paper. During the paper making process, 4.0 parts by mass (in terms of solid content) of potato starch was sprayed between the layers by interlayer spraying, and after 5 layers of papermaking, 4.0 g of oxidized starch was applied to the surface of the paper base material by a size press. /M 2 (solid content conversion) was applied to obtain a paper base material having a basis weight of 374 g/m 2 . The obtained paper substrate contained the linear fatty acid and linear alcohol shown in Table 1.
A gable-top type paper container was obtained in the same manner as in Example 1 except that the thermoplastic resin layer was laminated on the obtained paper base material so that the thickness and the weight were as shown in Table 1.

[実施例7]
パルプ原料としてLBKP10部(アカシア材30%、ユーカリ材70%)、NBKP90部(ダグラスファー50%、ラジアータパイン30%、スギ20%)を、それぞれダブルディスクレファイナーを使用して叩解し、パルプスラリーを得た。得られたパルプスラリー100部に対して、内添紙力増強剤としてカチオン化澱粉0.60部(固形分換算)、内添サイズ剤としてアルキルケテンダイマー系サイズ剤0.30部(固形分換算)、硫酸バンドを0.20部(固形分換算)、湿潤紙力剤として、ポリアミド・アミンエピクロロヒドリン系湿潤紙力剤を0.10質量部(固形分換算)を添加し紙料を調製した。この紙料を用いて5層抄きの長網抄紙機を用いて抄紙した。抄紙工程中、層間スプレーにて、各層間にバレイショ澱粉を3.0質量部(固形分換算)吹き付けるとともに、5層抄き合わせ後に、紙基材の表面にサイズプレスで酸化澱粉を2.3g/m(固形分換算)塗布し、坪量424g/mの紙基材を得た。得られた紙基材には、表1に記載の直鎖脂肪酸および直鎖アルコールが含まれていた。
得られた紙基材に、厚さ、質量を表1に記載の条件となるよう熱可塑性樹脂層をラミネートした以外は実施例1と同様にして、ゲーブルトップ型紙容器を得た。
[Example 7]
As a pulp raw material, 10 parts of LBKP (30% of acacia wood, 70% of eucalyptus wood) and 90 parts of NBKP (50% of Douglas fir, 30% of radiata pine, 20% of cedar) were beaten using a double disc refiner, respectively, to obtain a pulp slurry. Got With respect to 100 parts of the obtained pulp slurry, 0.60 parts of cationic starch (solid content conversion) as an internal paper strength enhancer and 0.30 part of alkyl ketene dimer sizing agent as solid addition size agent (solid content conversion) ), 0.20 part of sulfuric acid band (solid content conversion), and 0.10 parts by mass (solid content conversion) of a polyamide-amine epichlorohydrin-based wet paper strength agent as a wet paper strength agent. Prepared. Using this stock, a five-layer fourdrinier paper machine was used to make paper. During the papermaking process, 3.0 parts by mass (in terms of solid content) of potato starch was sprayed between the layers by interlayer spraying, and after 5 layers of papermaking, 2.3 g of oxidized starch was applied to the surface of the paper base material by a size press. /M 2 (solid content conversion) was applied to obtain a paper base material having a basis weight of 424 g/m 2 . The obtained paper substrate contained the linear fatty acid and linear alcohol shown in Table 1.
A gable-top type paper container was obtained in the same manner as in Example 1 except that the thermoplastic resin layer was laminated on the obtained paper base material so that the thickness and the weight were as shown in Table 1.

[実施例8]
パルプ原料としてLBKP10部(アカシア材20%、ユーカリ材80%)、NBKP90部(ダグラスファー50%、ラジアータパイン30%、スギ20%)を、それぞれダブルディスクレファイナーを使用して叩解し、パルプスラリーを得た。得られたパルプスラリー100部に対して、内添紙力増強剤としてカチオン化澱粉0.60部(固形分換算)、内添サイズ剤としてアルキルケテンダイマー系サイズ剤0.30部(固形分換算)、硫酸バンドを0.20部(固形分換算)、湿潤紙力剤として、ポリアミド・アミンエピクロロヒドリン系湿潤紙力剤を0.10質量部(固形分換算)を添加し紙料を調製した。この紙料を用いて5層抄きの長網抄紙機を用いて抄紙した。抄紙工程中、層間スプレーにて、各層間にバレイショ澱粉を3.0質量部(固形分換算)吹き付けるとともに、5層抄き合わせ後に、紙基材の表面にサイズプレスで酸化澱粉を2.3g/m(固形分換算)塗布し、坪量453g/mの紙基材を得た。得られた紙基材には、表1に記載の直鎖脂肪酸および直鎖アルコールが含まれていた。
得られた紙基材に、厚さ、質量を表1に記載の条件となるよう熱可塑性樹脂層をラミネートした以外は実施例1と同様にして、ゲーブルトップ型紙容器を得た。
[Example 8]
As a pulp raw material, 10 parts of LBKP (20% of acacia wood, 80% of eucalyptus wood) and 90 parts of NBKP (50% of Douglas fir, 30% of radiata pine, 20% of cedar) were beaten using a double disc refiner, respectively, to obtain a pulp slurry. Got With respect to 100 parts of the obtained pulp slurry, 0.60 parts of cationic starch (solid content conversion) as an internal paper strength enhancer and 0.30 part of alkyl ketene dimer sizing agent as solid addition size agent (solid content conversion) ), 0.20 part of sulfuric acid band (solid content conversion), and 0.10 parts by mass (solid content conversion) of a polyamide-amine epichlorohydrin-based wet paper strength agent as a wet paper strength agent. Prepared. Using this stock, a five-layer fourdrinier paper machine was used to make paper. During the papermaking process, 3.0 parts by mass (in terms of solid content) of potato starch was sprayed between the layers by interlayer spraying, and after 5 layers of papermaking, 2.3 g of oxidized starch was applied to the surface of the paper base material by a size press. /M 2 (solid content conversion) was applied to obtain a paper base material having a basis weight of 453 g/m 2 . The obtained paper substrate contained the linear fatty acid and linear alcohol shown in Table 1.
A gable-top type paper container was obtained in the same manner as in Example 1 except that the thermoplastic resin layer was laminated on the obtained paper base material so that the thickness and the weight were as shown in Table 1.

[比較例1]
パルプ原料としてLBKP80部(アカシア材100%)、NBKP20部(ダグラスファー50%、ラジアータパイン30%、スギ20%)を、それぞれダブルディスクレファイナーを使用して叩解し、パルプスラリーを得た。得られたパルプスラリー100部に対して、内添紙力増強剤としてカチオン化澱粉0.60部(固形分換算)、内添サイズ剤としてアルキルケテンダイマー系サイズ剤0.30部(固形分換算)、硫酸バンドを0.20部(固形分換算)、湿潤紙力剤として、ポリアミド・アミンエピクロロヒドリン系湿潤紙力剤を0.10質量部(固形分換算)を添加し紙料を調製した。この紙料を用いて4層抄きの長網抄紙機を用いて抄紙した。抄紙工程中、層間スプレーにて、各層間にバレイショ澱粉を3.0質量部(固形分換算)吹き付けるとともに、5層抄き合わせ後に、紙基材の表面にサイズプレスで酸化澱粉を2.3g/m(固形分換算)塗布し、坪量278g/mの紙基材を得た。得られた紙基材には、表1に記載の直鎖脂肪酸および直鎖アルコールが含まれていた。
得られた紙基材に、厚さ、質量を表1に記載の条件となるよう熱可塑性樹脂層をラミネートした以外は実施例1と同様にして、ゲーブルトップ型紙容器を得た。
[Comparative Example 1]
As a pulp raw material, 80 parts of LBKP (100% of acacia wood) and 20 parts of NBKP (50% of Douglas fir, 30% of radiata pine, 20% of cedar) were beaten using a double disc refiner to obtain a pulp slurry. With respect to 100 parts of the obtained pulp slurry, 0.60 parts of cationic starch (solid content conversion) as an internal paper strength enhancer and 0.30 part of alkyl ketene dimer sizing agent as solid addition size agent (solid content conversion) ), 0.20 part of sulfuric acid band (solid content conversion), and 0.10 parts by mass (solid content conversion) of a polyamide-amine epichlorohydrin-based wet paper strength agent as a wet paper strength agent. Prepared. Using this stock, a four-layer fourdrinier paper machine was used to make paper. During the papermaking process, 3.0 parts by mass (in terms of solid content) of potato starch was sprayed between the layers by interlayer spraying, and after 5 layers of papermaking, 2.3 g of oxidized starch was applied to the surface of the paper base material by a size press. /M 2 (solid content conversion) was applied to obtain a paper base material having a basis weight of 278 g/m 2 . The obtained paper substrate contained the linear fatty acid and linear alcohol shown in Table 1.
A gable-top type paper container was obtained in the same manner as in Example 1 except that the thermoplastic resin layer was laminated on the obtained paper base material so that the thickness and the weight were as shown in Table 1.

[比較例2]
パルプ原料としてLBKP80部(アカシア材90%、ユーカリ材10%)、NBKP20部(ダグラスファー50%、ラジアータパイン30%、スギ20%)を、それぞれダブルディスクレファイナーを使用して叩解し、パルプスラリーを得た。得られたパルプスラリー100部に対して、内添紙力増強剤としてカチオン化澱粉0.60部(固形分換算)、内添サイズ剤としてアルキルケテンダイマー系サイズ剤0.30部(固形分換算)、硫酸バンドを0.20部(固形分換算)、湿潤紙力剤として、ポリアミド・アミンエピクロロヒドリン系湿潤紙力剤を0.10質量部(固形分換算)を添加し紙料を調製した。この紙料を用いて5層抄きの長網抄紙機を用いて抄紙した。抄紙工程中、層間スプレーにて、各層間にバレイショ澱粉を3.0質量部(固形分換算)吹き付けるとともに、5層抄き合わせ後に、紙基材の表面にサイズプレスで酸化澱粉を2.3g/m(固形分換算)塗布し、坪量466g/mの紙基材を得た。得られた紙基材には、表1に記載の直鎖脂肪酸および直鎖アルコールが含まれていた。
得られた紙基材に、厚さ、質量を表1に記載の条件となるよう熱可塑性樹脂層をラミネートした以外は実施例1と同様にして、ゲーブルトップ型紙容器を得た。
[Comparative example 2]
As a pulp raw material, 80 parts of LBKP (90% of acacia wood, 10% of eucalyptus wood) and 20 parts of NBKP (50% of Douglas fir, 30% of radiata pine, 20% of cedar) were beaten using a double disc refiner, respectively, to obtain a pulp slurry. Got With respect to 100 parts of the obtained pulp slurry, 0.60 parts of cationic starch (solid content conversion) as an internal paper strength enhancer and 0.30 part of alkyl ketene dimer sizing agent as solid addition size agent (solid content conversion) ), 0.20 part of sulfuric acid band (solid content conversion), and 0.10 parts by mass (solid content conversion) of a polyamide-amine epichlorohydrin-based wet paper strength agent as a wet paper strength agent. Prepared. Using this stock, a five-layer fourdrinier paper machine was used to make paper. During the papermaking process, 3.0 parts by mass (in terms of solid content) of potato starch was sprayed between the layers by interlayer spraying, and after 5 layers of papermaking, 2.3 g of oxidized starch was applied to the surface of the paper base material by a size press. /M 2 (solid content conversion) was applied to obtain a paper base material having a basis weight of 466 g/m 2 . The obtained paper substrate contained the linear fatty acid and linear alcohol shown in Table 1.
A gable-top type paper container was obtained in the same manner as in Example 1 except that the thermoplastic resin layer was laminated on the obtained paper base material so that the thickness and the weight were as shown in Table 1.

[比較例3]
パルプ原料としてLBKP50部(アカシア材85%、ユーカリ材15%)、NBKP50部(ダグラスファー50%、ラジアータパイン30%、スギ20%)を、それぞれダブルディスクレファイナーを使用して叩解し、パルプスラリーを得た。得られたパルプスラリー100部に対して、内添紙力増強剤としてカチオン化澱粉0.60部(固形分換算)、内添サイズ剤としてアルキルケテンダイマー系サイズ剤0.30部(固形分換算)、硫酸バンドを0.20部(固形分換算)、湿潤紙力剤として、ポリアミド・アミンエピクロロヒドリン系湿潤紙力剤を0.10質量部(固形分換算)を添加し紙料を調製した。この紙料を用いて3層抄きの長網抄紙機を用いて抄紙した。抄紙工程中、層間スプレーにて、各層間にバレイショ澱粉を3.0質量部(固形分換算)吹き付けるとともに、5層抄き合わせ後に、紙基材の表面にサイズプレスで酸化澱粉を2.3g/m(固形分換算)塗布し、坪量119g/mの紙基材を得た。得られた紙基材には、表1に記載の直鎖脂肪酸および直鎖アルコールが含まれていた。
得られた紙基材に、厚さ、質量を表1に記載の条件となるよう熱可塑性樹脂層をラミネートした以外は実施例1と同様にして、ゲーブルトップ型紙容器を得た。
[Comparative Example 3]
50 parts LBKP (acacia wood 85%, eucalyptus wood 15%) and NBKP 50 parts (Douglas fir 50%, radiata pine 30%, cedar 20%) as pulp raw materials were beaten using a double disc refiner, respectively, to obtain a pulp slurry. Got With respect to 100 parts of the obtained pulp slurry, 0.60 parts of cationic starch (solid content conversion) as an internal paper strength enhancer and 0.30 part of alkyl ketene dimer sizing agent as solid addition size agent (solid content conversion) ), 0.20 part of sulfuric acid band (solid content conversion), and 0.10 parts by mass (solid content conversion) of a polyamide-amine epichlorohydrin-based wet paper strength agent as a wet paper strength agent. Prepared. Using this stock, paper was made using a four-layer fourdrinier paper machine. During the papermaking process, 3.0 parts by mass (in terms of solid content) of potato starch was sprayed between the layers by interlayer spraying, and after 5 layers of papermaking, 2.3 g of oxidized starch was applied to the surface of the paper base material by a size press. /M 2 (solid content conversion) was applied to obtain a paper base material having a basis weight of 119 g/m 2 . The obtained paper substrate contained the linear fatty acid and linear alcohol shown in Table 1.
A gable-top type paper container was obtained in the same manner as in Example 1 except that the thermoplastic resin layer was laminated on the obtained paper base material so that the thickness and the weight were as shown in Table 1.

[比較例4]
パルプ原料としてLBKP50部(アカシア材15%、ユーカリ材85%)、NBKP50部(ダグラスファー50%、ラジアータパイン30%、スギ20%)を、それぞれダブルディスクレファイナーを使用して叩解し、パルプスラリーを得た。得られたパルプスラリー100部に対して、内添紙力増強剤としてカチオン化澱粉0.60部(固形分換算)、内添サイズ剤としてアルキルケテンダイマー系サイズ剤0.30部(固形分換算)、硫酸バンドを0.20部(固形分換算)、湿潤紙力剤として、ポリアミド・アミンエピクロロヒドリン系湿潤紙力剤を0.10質量部(固形分換算)を添加し紙料を調製した。この紙料を用いて5層抄きの長網抄紙機を用いて抄紙した。抄紙工程中、層間スプレーにて、各層間にバレイショ澱粉を3.0質量部(固形分換算)吹き付けるとともに、5層抄き合わせ後に、紙基材の表面にサイズプレスで酸化澱粉を2.3g/m(固形分換算)塗布し、坪量377g/mの紙基材を得た。得られた紙基材には、表1に記載の直鎖脂肪酸および直鎖アルコールが含まれていた。
得られた紙基材に、厚さ、質量を表1に記載の条件となるよう熱可塑性樹脂層をラミネートした以外は実施例1と同様にして、ゲーブルトップ型紙容器を得た。
[Comparative Example 4]
50 parts of LBKP (15% of acacia wood, 85% of eucalyptus wood) and 50 parts of NBKP (50% Douglas fir, 30% radiata pine, 20% cedar) as pulp raw materials were beaten using a double disc refiner to produce a pulp slurry. Got With respect to 100 parts of the obtained pulp slurry, 0.60 parts of cationic starch (solid content conversion) as an internal paper strength enhancer and 0.30 part of alkyl ketene dimer sizing agent as solid addition size agent (solid content conversion) ), 0.20 part of sulfuric acid band (solid content conversion), and 0.10 parts by mass (solid content conversion) of a polyamide-amine epichlorohydrin-based wet paper strength agent as a wet paper strength agent. Prepared. Using this stock, a five-layer fourdrinier paper machine was used to make paper. During the papermaking process, 3.0 parts by mass (in terms of solid content) of potato starch was sprayed between the layers by interlayer spraying, and after 5 layers of papermaking, 2.3 g of oxidized starch was applied to the surface of the paper base material by a size press. /M 2 (solid content conversion) was applied to obtain a paper base material having a basis weight of 377 g/m 2 . The obtained paper substrate contained the linear fatty acid and linear alcohol shown in Table 1.
A gable-top type paper container was obtained in the same manner as in Example 1 except that the thermoplastic resin layer was laminated on the obtained paper base material so that the thickness and the weight were as shown in Table 1.

[比較例5]
パルプ原料としてNBKP100部(ダグラスファー50%、ラジアータパイン30%、スギ20%)を、ダブルディスクレファイナーを使用して叩解し、パルプスラリーを得た。得られたパルプスラリー100部に対して、内添紙力増強剤としてカチオン化澱粉0.60部(固形分換算)、内添サイズ剤としてアルキルケテンダイマー系サイズ剤0.30部(固形分換算)、硫酸バンドを0.20部(固形分換算)、湿潤紙力剤として、ポリアミド・アミンエピクロロヒドリン系湿潤紙力剤を0.10質量部(固形分換算)を添加し紙料を調製した。この紙料を用いて5層抄きの長網抄紙機を用いて抄紙した。抄紙工程中、層間スプレーにて、各層間にバレイショ澱粉を3.0質量部(固形分換算)吹き付けるとともに、5層抄き合わせ後に、紙基材の表面にサイズプレスで酸化澱粉を2.3g/m(固形分換算)塗布し、坪量421g/mの紙基材を得た。得られた紙基材には、表1に記載の直鎖脂肪酸および直鎖アルコールが含まれていた。
得られた紙基材に、厚さ、質量を表1に記載の条件となるよう熱可塑性樹脂層をラミネートした以外は実施例1と同様にして、ゲーブルトップ型紙容器を得た。
[Comparative Example 5]
As a pulp raw material, 100 parts of NBKP (Douglas fir 50%, radiata pine 30%, cedar 20%) was beaten using a double disc refiner to obtain a pulp slurry. With respect to 100 parts of the obtained pulp slurry, 0.60 parts of cationic starch (solid content conversion) as an internal paper strength enhancer and 0.30 part of alkyl ketene dimer sizing agent as solid addition size agent (solid content conversion) ), 0.20 part of sulfuric acid band (solid content conversion), and 0.10 parts by mass (solid content conversion) of a polyamide-amine epichlorohydrin-based wet paper strength agent as a wet paper strength agent. Prepared. Using this stock, a five-layer fourdrinier paper machine was used to make paper. During the papermaking process, 3.0 parts by mass (in terms of solid content) of potato starch was sprayed between the layers by interlayer spraying, and after 5 layers of papermaking, 2.3 g of oxidized starch was applied to the surface of the paper base material by a size press. /M 2 (solid content conversion) was applied to obtain a paper base material having a basis weight of 421 g/m 2 . The obtained paper substrate contained the linear fatty acid and linear alcohol shown in Table 1.
A gable-top type paper container was obtained in the same manner as in Example 1 except that the thermoplastic resin layer was laminated on the obtained paper base material so that the thickness and the weight were as shown in Table 1.

[比較例6]
パルプ原料としてNBKP100部(ダグラスファー50%、ラジアータパイン30%、スギ20%)を、ダブルディスクレファイナーを使用して叩解し、パルプスラリーを得た。得られたパルプスラリー100部に対して、内添紙力増強剤としてカチオン化澱粉0.60部(固形分換算)、内添サイズ剤としてアルキルケテンダイマー系サイズ剤0.30部(固形分換算)、硫酸バンドを0.20部(固形分換算)、湿潤紙力剤として、ポリアミド・アミンエピクロロヒドリン系湿潤紙力剤を0.10質量部(固形分換算)を添加し紙料を調製した。この紙料を用いて5層抄きの長網抄紙機を用いて抄紙した。抄紙工程中、層間スプレーにて、各層間にバレイショ澱粉を3.0質量部(固形分換算)吹き付けるとともに、5層抄き合わせ後に、紙基材の表面にサイズプレスで酸化澱粉を2.3g/m(固形分換算)塗布し、坪量514g/mの紙基材を得た。得られた紙基材には、表1に記載の直鎖脂肪酸および直鎖アルコールが含まれていた。
得られた紙基材に、厚さ、質量を表1に記載の条件となるよう熱可塑性樹脂層をラミネートした以外は実施例1と同様にして、ゲーブルトップ型紙容器を得た。
[Comparative Example 6]
As a pulp raw material, 100 parts of NBKP (Douglas fir 50%, radiata pine 30%, cedar 20%) was beaten using a double disc refiner to obtain a pulp slurry. With respect to 100 parts of the obtained pulp slurry, 0.60 parts of cationic starch (solid content conversion) as an internal paper strength enhancer and 0.30 part of alkyl ketene dimer sizing agent as solid addition size agent (solid content conversion) ), 0.20 part of sulfuric acid band (solid content conversion), and 0.10 parts by mass (solid content conversion) of a polyamide-amine epichlorohydrin-based wet paper strength agent as a wet paper strength agent. Prepared. Using this stock, a five-layer fourdrinier paper machine was used to make paper. During the papermaking process, 3.0 parts by mass (in terms of solid content) of potato starch was sprayed between the layers by interlayer spraying, and after 5 layers of papermaking, 2.3 g of oxidized starch was applied to the surface of the paper base material by a size press. /M 2 (solid content conversion) was applied to obtain a paper base material having a basis weight of 514 g/m 2 . The obtained paper substrate contained the linear fatty acid and linear alcohol shown in Table 1.
A gable-top type paper container was obtained in the same manner as in Example 1 except that the thermoplastic resin layer was laminated on the obtained paper base material so that the thickness and the weight were as shown in Table 1.

以上のようにして得られたラミネート紙について以下の性能評価を行った。性能評価は、ラミネート紙の平滑性、ラミネート紙の剥離性、抄紙汚れの発生程度については、◎、○または△のとき合格と判定した。ラミネート紙の接着性については、◎または○のとき合格と判定した。評価結果は表1に記載のとおりであった。 The following performance evaluation was performed on the laminated paper obtained as described above. The performance evaluation was judged to be acceptable when the smoothness of the laminated paper, the peelability of the laminated paper, and the degree of paper stains were ⊚, ○ or Δ. Regarding the adhesiveness of the laminated paper, it was judged to be acceptable when ◎ or ○. The evaluation results are as shown in Table 1.

(ラミネート紙の平滑性)
実施例および比較例で得られたゲーブルトップ型紙容器のラミネート紙について、JIS P8155:2010に従い、王研式平滑度を測定した。王研式平滑度が250秒以上であれば◎、200秒以上であれば○、100秒以上であれば△、100秒未満であれば×とした。
(Smoothness of laminated paper)
The Oken type smoothness was measured according to JIS P8155:2010 for the laminated paper of the gable-top type paper containers obtained in Examples and Comparative Examples. When the Oken type smoothness was 250 seconds or more, it was evaluated as ⊚, when it was 200 seconds or more, it was evaluated as ◯, when 100 seconds or more was evaluated as Δ, and when it was less than 100 seconds, it was evaluated as x.

(ラミネート紙の接着性)
実施例および比較例で得られたゲーブルトップ型紙容器のラミネート紙について、熱可塑性樹脂層のラミネート後、23℃50%の調湿条件で1ヶ月保管した後に、、JIS K6854−3:1999に従い、熱可塑性樹脂層と紙基材間の接着強度を測定した。試験片幅25mm、接着部の長さを150mmとし、接着部の両端25mmを除く100mmの領域における剥離の程度を目視にて◎、○、△、×で評価した。剥離がみられず、十分に接着していれば◎、極一部の箇所でのみ剥離がみられれば○、極一部の箇所で剥離がみられ、かつその剥離範囲が広い場合は△、剥離が複数個所でみられた場合は×と評価した。
(Adhesiveness of laminated paper)
Regarding the laminated paper of the gable top type paper containers obtained in Examples and Comparative Examples, after laminating the thermoplastic resin layer, after storing for 1 month at 23° C. and 50% humidity control conditions, according to JIS K6854-3:1999, The adhesive strength between the thermoplastic resin layer and the paper substrate was measured. The width of the test piece was 25 mm, the length of the bonded portion was 150 mm, and the degree of peeling in a 100 mm region excluding 25 mm at both ends of the bonded portion was visually evaluated by ⊚, ◯, Δ, and x. No peeling was observed and sufficient adhesion was indicated by ⊚, peeling was observed only in a very small portion of the circle ○, peeling was observed in a very small portion of the peeling area, and the peeling range was wide, Δ, When peeling was observed at a plurality of places, it was evaluated as x.

(ラミネート紙の剥離性)
実施例および比較例で得られたゲーブルトップ型紙容器のラミネート紙について、熱可塑性樹脂層のラミネート後、23℃50%の調湿条件で12ヶ月保管した後に、5cm角の紙片に裁断し、JISP8220−1:2012に記載の標準離解機を用いて、23℃の水で1分間離解を行った。1分経過後の離解紙片を回収し、その8割以上の紙片において、端部から2.0cm以上の領域に掛けて熱可塑性樹脂層と紙基材の剥離がみられれば◎、1.5cm以上2.0cm以下の剥離が見られれば○、1.0cm以上1.5cm以下の剥離がみられれば△、剥離が1.0cm以下であれば×と評価した。
(Peelability of laminated paper)
Regarding the laminated paper of the gable-top type paper containers obtained in Examples and Comparative Examples, after laminating the thermoplastic resin layer, the laminated paper was stored for 12 months at a humidity condition of 23° C. and 50%, and then cut into 5 cm square pieces, and JISP8220 was used. Using a standard disintegrator described in −1:2012, disintegration was performed with water at 23° C. for 1 minute. Collect the disintegrated paper piece after 1 minute, and if 80% or more of the disintegrated paper piece is applied to an area of 2.0 cm or more from the edge and peeling of the thermoplastic resin layer and the paper base material is observed, ◎, 1.5 cm When the peeling of 2.0 cm or less was observed, it was evaluated as O, when the peeling of 1.0 cm or more and 1.5 cm or less was evaluated as Δ, and when the peeling was 1.0 cm or less, it was evaluated as x.

(抄紙汚れの発生程度)
実施例および比較例で得た紙基材を抄造した際の抄紙汚れの発生頻度を◎、○、△、×で評価した。得られた紙基材100gに相当する面積における、0.05mm以上のチリ個数を測定し、チリの数が0であれば◎、1〜2個であれば○、3〜5個であれば△、5個以上であれば×とした。
(Amount of paper stain)
The frequency of occurrence of paper stains when the paper base materials obtained in Examples and Comparative Examples were made was evaluated by ⊚, ◯, Δ, and x. The number of dust particles of 0.05 mm 2 or more in an area corresponding to 100 g of the obtained paper base material was measured. If the number of dust particles was 0, it was ⊚; If it is 5 or more, it is marked with x.

Figure 0006702496
Figure 0006702496

表1の結果から分かるように、実施例1〜実施例8のラミネート紙は、原紙の平滑性、ラミネート紙の接着性、ラミネート紙の剥離性、抄紙汚れの発生程度において、いずれも優れていた。比較例1〜6のラミネート紙は、原紙の平滑性、ラミネート紙の接着性、ラミネート紙の剥離性、抄紙汚れの発生程度のいずれかの性能において劣っていた。 As can be seen from the results in Table 1, the laminated papers of Examples 1 to 8 were all excellent in the smoothness of the base paper, the adhesiveness of the laminated paper, the peelability of the laminated paper, and the degree of paper stain. .. The laminated papers of Comparative Examples 1 to 6 were inferior in any of the smoothness of the base paper, the adhesiveness of the laminated paper, the releasability of the laminated paper, and the degree of paper stain.

Claims (12)

セルロースパルプを主成分とする紙基材と、当該紙基材の少なくとも一方の面上に積層された熱可塑性樹脂層とを有する紙容器用ラミネート紙であって、
前記紙基材は、直鎖脂肪酸および直鎖アルコールの少なくとも1種を含有し、
前記直鎖脂肪酸および前記直鎖アルコールの融点が80〜100℃であり、
前記紙基材中の前記直鎖脂肪酸および前記直鎖アルコールの含有量の合計が100〜2500ppmであることを特徴とする紙容器用ラミネート紙。
A laminated paper for a paper container having a paper base material mainly composed of cellulose pulp, and a thermoplastic resin layer laminated on at least one surface of the paper base material,
The paper substrate contains at least one of a linear fatty acid and a linear alcohol,
The linear fatty acid and the linear alcohol have a melting point of 80 to 100° C.,
A laminated paper for a paper container, wherein the total content of the linear fatty acid and the linear alcohol in the paper substrate is 100 to 2500 ppm.
前記直鎖脂肪酸の炭素数が24、26または28であり、前記直鎖アルコールの炭素数が26または28である請求項1に記載の紙容器用ラミネート紙。 The laminated paper for a paper container according to claim 1, wherein the linear fatty acid has 24, 26 or 28 carbon atoms, and the linear alcohol has 26 or 28 carbon atoms. 前記紙基材が前記直鎖脂肪酸および前記直鎖アルコールの両者を含有し、
前記直鎖脂肪酸の含有量に対する前記直鎖アルコールの含有量の比率が、3.0〜33.3%である請求項1または請求項2に記載の紙容器用ラミネート紙。
The paper substrate contains both the linear fatty acid and the linear alcohol,
The laminated paper for paper containers according to claim 1 or 2, wherein a ratio of the content of the linear alcohol to the content of the linear fatty acid is 3.0 to 33.3%.
カヤーニファイバーラボで測定される前記紙基材の離解原料の繊維粗度が0.020〜0.18mg/mである請求項1〜3のいずれか1項に記載の紙容器用ラミネート紙。 The laminated paper for a paper container according to any one of claims 1 to 3, wherein the fiber roughness of the disaggregation raw material of the paper substrate measured by Kajaani Fiber Lab is 0.020 to 0.18 mg/m. 坪量が150〜500g/mである請求項1〜4のいずれか1項に記載の紙容器用ラミネート紙。 The laminated paper for paper containers according to any one of claims 1 to 4, which has a basis weight of 150 to 500 g/m 2 . 前記紙基材が多層紙である請求項1〜5のいずれか1項に記載の紙容器用ラミネート紙。 The laminated paper for a paper container according to any one of claims 1 to 5, wherein the paper base material is a multi-layered paper. セルロースパルプを主成分とする紙容器用ラミネート紙用紙基材であって、
直鎖脂肪酸および直鎖アルコールの少なくとも1種を含有し、
前記直鎖脂肪酸および前記直鎖アルコールの融点が80〜100℃であり、
前記直鎖脂肪酸および前記直鎖アルコールの含有量の合計が100〜2500ppmであることを特徴とする紙容器用ラミネート紙用紙基材。
A laminated paper paper base material for a paper container containing cellulose pulp as a main component,
Contains at least one of a straight chain fatty acid and a straight chain alcohol,
The linear fatty acid and the linear alcohol have a melting point of 80 to 100° C.,
A laminated paper paper base material for paper containers, wherein the total content of the linear fatty acid and the linear alcohol is 100 to 2500 ppm.
多層紙である請求項7に記載の紙容器用ラミネート紙用紙基材。 The laminated paper paper base material for a paper container according to claim 7, which is a multi-layered paper. 請求項1〜のいずれか1項に記載の紙容器用ラミネート紙を用いた紙容器。 Paper container with laminated paper for paper container according to any one of claims 1-5. 液体用である請求項9に記載の紙容器。 The paper container according to claim 9, which is for a liquid. 請求項1〜6のいずれか1項に記載の紙容器用ラミネート紙の製造方法であって、
セルロースパルプを主成分とする紙基材の抄紙工程と、
前記紙基材の少なくとも一方の面上に熱可塑性樹脂層を積層するラミネート工程とを有し、
前記抄紙工程および前記ラミネート工程の少なくともいずれかの工程で、前記紙基材に100℃以上に加熱された物を接触させることを特徴とする紙容器用ラミネート紙の製造方法。
A method for manufacturing a laminated paper for a paper container according to any one of claims 1 to 6, comprising:
A paper-making process of a paper base material whose main component is cellulose pulp,
A laminating step of laminating a thermoplastic resin layer on at least one surface of the paper substrate,
A method for producing a laminated paper for a paper container, which comprises bringing a material heated to 100° C. or higher into contact with the paper base material in at least one of the paper making step and the laminating step.
前記紙基材が多層紙であって、前記抄紙工程において、多層抄き用抄紙機を用いて前記紙基材を抄紙することを特徴とする請求項11に記載の紙容器用ラミネート紙の製造方法。 12. The laminated paper for a paper container according to claim 11, wherein the paper substrate is a multi-layered paper, and the paper substrate is paper-made by using a multi-layer paper machine in the paper making step. Method.
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