JP2020133023A - Base paper for release paper and release paper - Google Patents
Base paper for release paper and release paper Download PDFInfo
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- JP2020133023A JP2020133023A JP2019026049A JP2019026049A JP2020133023A JP 2020133023 A JP2020133023 A JP 2020133023A JP 2019026049 A JP2019026049 A JP 2019026049A JP 2019026049 A JP2019026049 A JP 2019026049A JP 2020133023 A JP2020133023 A JP 2020133023A
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- release paper
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- 239000001023 inorganic pigment Substances 0.000 claims abstract description 49
- 238000007789 sealing Methods 0.000 claims abstract description 46
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 43
- 238000000576 coating method Methods 0.000 claims abstract description 35
- 239000011248 coating agent Substances 0.000 claims abstract description 34
- 239000004816 latex Substances 0.000 claims abstract description 33
- 229920000126 latex Polymers 0.000 claims abstract description 33
- 229920002050 silicone resin Polymers 0.000 claims abstract description 31
- 239000000049 pigment Substances 0.000 claims abstract description 25
- 229920003002 synthetic resin Polymers 0.000 claims abstract description 25
- 239000000057 synthetic resin Substances 0.000 claims abstract description 25
- 239000000853 adhesive Substances 0.000 claims abstract description 22
- 230000001070 adhesive effect Effects 0.000 claims abstract description 22
- MZZSDCJQCLYLLL-UHFFFAOYSA-N Secalonsaeure A Natural products COC(=O)C12OC3C(CC1=C(O)CC(C)C2O)C(=CC=C3c4ccc(O)c5C(=O)C6=C(O)CC(C)C(O)C6(Oc45)C(=O)OC)O MZZSDCJQCLYLLL-UHFFFAOYSA-N 0.000 claims abstract description 20
- 238000002156 mixing Methods 0.000 claims abstract description 13
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical group [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims description 34
- 238000000034 method Methods 0.000 claims description 31
- 229910000019 calcium carbonate Inorganic materials 0.000 claims description 17
- 239000005995 Aluminium silicate Substances 0.000 claims description 11
- 235000012211 aluminium silicate Nutrition 0.000 claims description 11
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 claims description 11
- 239000002245 particle Substances 0.000 claims description 9
- 229920001577 copolymer Polymers 0.000 claims description 7
- 230000003746 surface roughness Effects 0.000 claims description 7
- 238000007561 laser diffraction method Methods 0.000 claims description 4
- 238000000790 scattering method Methods 0.000 claims description 4
- 230000009477 glass transition Effects 0.000 claims description 3
- -1 polyethylene Polymers 0.000 abstract description 7
- 229920005989 resin Polymers 0.000 abstract description 7
- 239000011347 resin Substances 0.000 abstract description 7
- 239000004698 Polyethylene Substances 0.000 abstract description 6
- 229920000573 polyethylene Polymers 0.000 abstract description 6
- 238000010030 laminating Methods 0.000 abstract description 5
- 239000002904 solvent Substances 0.000 abstract description 5
- 239000000123 paper Substances 0.000 description 188
- 239000010410 layer Substances 0.000 description 53
- 230000000052 comparative effect Effects 0.000 description 16
- 238000001035 drying Methods 0.000 description 9
- 238000011156 evaluation Methods 0.000 description 9
- 239000007788 liquid Substances 0.000 description 9
- 239000002655 kraft paper Substances 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 229920003048 styrene butadiene rubber Polymers 0.000 description 6
- 229920001131 Pulp (paper) Polymers 0.000 description 5
- 230000007547 defect Effects 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- 239000000839 emulsion Substances 0.000 description 4
- 239000000835 fiber Substances 0.000 description 4
- 239000000945 filler Substances 0.000 description 4
- 238000013441 quality evaluation Methods 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 3
- 239000004927 clay Substances 0.000 description 3
- 238000009826 distribution Methods 0.000 description 3
- 239000007921 spray Substances 0.000 description 3
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 description 2
- 229920002472 Starch Polymers 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 229920002522 Wood fibre Polymers 0.000 description 2
- 239000002390 adhesive tape Substances 0.000 description 2
- 239000002518 antifoaming agent Substances 0.000 description 2
- 239000011247 coating layer Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000010494 dissociation reaction Methods 0.000 description 2
- 230000005593 dissociations Effects 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- 238000004043 dyeing Methods 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 239000000314 lubricant Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000011087 paperboard Substances 0.000 description 2
- 230000035699 permeability Effects 0.000 description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 238000004513 sizing Methods 0.000 description 2
- 239000008107 starch Substances 0.000 description 2
- 235000019698 starch Nutrition 0.000 description 2
- 239000000454 talc Substances 0.000 description 2
- 229910052623 talc Inorganic materials 0.000 description 2
- 239000013053 water resistant agent Substances 0.000 description 2
- 239000002025 wood fiber Substances 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 235000017166 Bambusa arundinacea Nutrition 0.000 description 1
- 235000017491 Bambusa tulda Nutrition 0.000 description 1
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 1
- 244000025254 Cannabis sativa Species 0.000 description 1
- 235000012766 Cannabis sativa ssp. sativa var. sativa Nutrition 0.000 description 1
- 235000012765 Cannabis sativa ssp. sativa var. spontanea Nutrition 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 240000000797 Hibiscus cannabinus Species 0.000 description 1
- 229920000881 Modified starch Polymers 0.000 description 1
- 239000004368 Modified starch Substances 0.000 description 1
- 244000082204 Phyllostachys viridis Species 0.000 description 1
- 235000015334 Phyllostachys viridis Nutrition 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 229910021536 Zeolite Inorganic materials 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 229920006243 acrylic copolymer Polymers 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000011425 bamboo Substances 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 235000009120 camo Nutrition 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 229920006319 cationized starch Polymers 0.000 description 1
- 235000005607 chanvre indien Nutrition 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 1
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 239000003623 enhancer Substances 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 239000006081 fluorescent whitening agent Substances 0.000 description 1
- 150000002222 fluorine compounds Chemical class 0.000 description 1
- 239000011121 hardwood Substances 0.000 description 1
- 239000011487 hemp Substances 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000003550 marker Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229910052901 montmorillonite Inorganic materials 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000001254 oxidized starch Substances 0.000 description 1
- 235000013808 oxidized starch Nutrition 0.000 description 1
- 239000003002 pH adjusting agent Substances 0.000 description 1
- 239000013054 paper strength agent Substances 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 239000012466 permeate Substances 0.000 description 1
- 239000011295 pitch Substances 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 229920000728 polyester Chemical class 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 230000002335 preservative effect Effects 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 229910000275 saponite Inorganic materials 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
Landscapes
- Paper (AREA)
Abstract
Description
本発明は、粘着ラベル、粘着シール、粘着テープ等に使用する剥離紙に用いられる剥離紙用原紙に関し、特に、原紙上にポリエチレン等の樹脂をラミネートすることなく、剥離剤である溶剤系シリコーン樹脂、水系エマルジョン系シリコーン樹脂又は無溶剤系シリコーン樹脂を直接塗工することが可能である剥離紙用原紙、及び、該原紙に剥離剤を塗工することによって得られる、優れた密着性、剥離性、離解性を有する剥離紙に関する。 The present invention relates to a release paper base paper used for a release paper used for an adhesive label, an adhesive sticker, an adhesive tape, etc., and in particular, a solvent-based silicone resin which is a release agent without laminating a resin such as polyethylene on the base paper. , A base paper for release paper that can be directly coated with a water-based emulsion-based silicone resin or a solvent-free silicone resin, and excellent adhesion and peelability obtained by applying a release agent to the base paper. , Releasable release paper.
剥離紙は、粘着ラベル、粘着シール、粘着テープ等の、粘着面に、ごみ等が付着しないように保護するための台紙として用いられ、該粘着面と接する表面には、シリコーン樹脂等の剥離剤が塗工されている。
従来の剥離紙は、ポリエチレン等の樹脂ラミネート紙、グラシン紙、クレーコート紙、クリアコート紙等の原紙の表面に、剥離剤を塗工して製造するが、これらの剥離剤は、トルエン等の有機溶剤で希釈して使用するため、環境破壊を引き起こすという問題があった。
そこで、近年においては、水系エマルジョン型のシリコーン樹脂や、無溶剤系シリコーン樹脂に対する需要が高くなっている。
The release paper is used as a mount for protecting the adhesive surface of adhesive labels, adhesive stickers, adhesive tapes, etc. from dust and the like, and a release agent such as silicone resin is used on the surface in contact with the adhesive surface. Is painted.
Conventional release paper is manufactured by applying a release agent to the surface of base paper such as resin laminated paper such as polyethylene, glassin paper, clay coated paper, and clear coated paper. These release agents are made of toluene or the like. Since it is diluted with an organic solvent and used, there is a problem of causing environmental damage.
Therefore, in recent years, there has been an increasing demand for water-based emulsion-type silicone resins and solvent-free silicone resins.
また、剥離剤として使用するシリコーン樹脂は非常に高価であるので、少量のシリコーン樹脂塗工液を均一に塗工することを可能にするために、シリコーン樹脂塗工液が原紙の内部に浸透することを極力抑えることが剥離紙用原紙の特性として必要である。また、近年においては、省資源の観点から、リサイクル性も求められるようになっている。 In addition, since the silicone resin used as a release agent is very expensive, the silicone resin coating liquid permeates the inside of the base paper in order to enable uniform coating of a small amount of the silicone resin coating liquid. It is necessary as a characteristic of the base paper for release paper to suppress this as much as possible. In recent years, recyclability has also been required from the viewpoint of resource saving.
シリコーン樹脂等の剥離剤の浸透を抑制するためには、原紙にポリエチレン等の樹脂をラミネートした剥離紙用原紙が好適であるが、使用後の剥離紙の離解が困難であるため、リサイクル性が劣るという問題があった。 In order to suppress the penetration of a release agent such as a silicone resin, a release paper base paper obtained by laminating a resin such as polyethylene on a base paper is preferable, but since it is difficult to separate the release paper after use, it is recyclable. There was a problem of inferiority.
上記問題を解決するために、シリコーン樹脂塗工液の原紙内部への浸透を防止するために、顔料と合成ラテックスからなる顔料塗工層を設けた、リサイクルが可能な剥離紙用原紙に関する発明が開示されている(特許文献1等)。しかし、シリコーン樹脂塗工液の浸透が十分に防止されず、十分な密着性、剥離性、離解性を有する剥離紙を得ることはできなかった。 In order to solve the above problem, an invention relating to a recyclable release paper base paper provided with a pigment coating layer composed of a pigment and a synthetic latex in order to prevent the silicone resin coating liquid from penetrating into the base paper has been invented. It is disclosed (Patent Document 1 etc.). However, the permeation of the silicone resin coating liquid was not sufficiently prevented, and it was not possible to obtain a release paper having sufficient adhesion, peelability, and disintegration property.
そこで、本発明は、原紙上にポリエチレン等の樹脂をラミネートすることなく、剥離剤である溶剤系シリコーン樹脂、水系エマルジョン系シリコーン樹脂又は無溶剤系シリコーン樹脂を直接塗工することが可能である剥離紙用原紙、及び、該剥離紙用原紙に剥離剤を塗工することによって得られる、優れた密着性、剥離性、離解性を有する剥離紙を提供することを目的とする。 Therefore, according to the present invention, it is possible to directly apply a solvent-based silicone resin, an aqueous emulsion-based silicone resin, or a solvent-free silicone resin as a release agent without laminating a resin such as polyethylene on the base paper. It is an object of the present invention to provide a base paper for paper and a release paper having excellent adhesion, peelability, and releasability obtained by applying a release agent to the base paper for release paper.
本発明は、以下の〔1〕〜〔12〕を提供するものである。
〔1〕基紙の少なくとも一方の面に、少なくとも顔料成分及び接着剤成分を含有する目止め層を設けてなる剥離紙用原紙であって、前記顔料成分としてアスペクト比が10以上である無機顔料A及びアスペクト比が10未満である無機顔料Bを含有し、前記無機顔料Aと前記無機顔料Bの配合比率が質量比で95/5〜50/50であり、前記接着剤成分が少なくとも合成樹脂ラテックスを含有すると共に、前記顔料成分の絶乾100質量部に対する該合成樹脂ラテックスの配合量が、絶乾で20〜50質量部であることを特徴とする剥離紙用原紙。
〔2〕前記無機顔料Bのレーザー回折/散乱法で測定した体積50%平均粒子径(D50)が0.5〜2.0μmであることを特徴とする〔1〕に記載の剥離紙用原紙。
〔3〕前記無機顔料Bが炭酸カルシウムであることを特徴とする〔1〕または〔2〕に記載の剥離紙用原紙。
〔4〕前記炭酸カルシウムが軽質炭酸カルシウムであることを特徴とする〔3〕に記載の剥離紙用原紙。
〔5〕前記無機顔料Aがカオリンであることを特徴とする〔1〕〜〔4〕のいずれかに記載の剥離紙用原紙。
〔6〕前記合成樹脂ラテックスのガラス転移温度が−20〜30℃であることを特徴とする〔1〕〜〔5〕のいずれかに記載の剥離紙用原紙。
〔7〕前記合成樹脂ラテックスがスチレン・ブダジエン系共重合体ラテックスであることを特徴とする〔1〕〜〔6〕のいずれかに記載の剥離紙用原紙。
〔8〕JIS P 8111:1998の環境下でJIS P 8124:2011に基づいて測定した、基紙と剥離紙用原紙との坪量差より求める前記目止め層の塗工量が、8〜20g/m2であることを特徴とする〔1〕〜〔7〕のいずれかに記載の剥離紙用原紙。〔9〕前記目止め層表面の、JIS B 0601:1994に基づいて測定した表面粗さが0.5〜1.0μmであることを特徴とする〔1〕〜〔8〕のいずれかに記載された剥離紙用原紙。
〔10〕JIS P 8117:2009に規定される透気抵抗度(王研式試験機法)が100,000秒以上であることを特徴とする〔1〕〜〔9〕のいずれかに記載の剥離紙用原紙。
〔11〕〔1〕〜〔10〕のいずれかに記載の剥離紙用原紙の目止め層上に剥離剤層を有する剥離紙であって、JIS P 8111:1998の環境下で、JIS P 8124:2011に基づいて測定した、前記剥離紙用原紙と前記剥離紙の坪量差より求める前記剥離剤層の塗工量が0.5〜2.0g/m2であることを特徴とする剥離紙。
〔12〕前記剥離剤層がシリコーン樹脂層であることを特徴とする〔11〕に記載の剥離紙。
なお、本発明において「絶乾」とは105℃で1〜2時間乾燥することをいい、以下、本発明で使用する顔料及び合成樹脂ラテックスの質量部は「絶乾後の質量部」とする。
The present invention provides the following [1] to [12].
[1] An inorganic pigment having an aspect ratio of 10 or more as the pigment component, which is a base paper for release paper provided with a sealing layer containing at least a pigment component and an adhesive component on at least one surface of the base paper. It contains A and an inorganic pigment B having an aspect ratio of less than 10, the blending ratio of the inorganic pigment A and the inorganic pigment B is 95/5 to 50/50 by mass, and the adhesive component is at least a synthetic resin. A base paper for release paper, which contains a latex and contains 20 to 50 parts by mass of the synthetic resin latex in an absolute dry state with respect to 100 parts by mass of the pigment component.
[2] The base paper for release paper according to [1], wherein the 50% volume average particle diameter (D50) measured by the laser diffraction / scattering method of the inorganic pigment B is 0.5 to 2.0 μm. ..
[3] The base paper for release paper according to [1] or [2], wherein the inorganic pigment B is calcium carbonate.
[4] The base paper for release paper according to [3], wherein the calcium carbonate is light calcium carbonate.
[5] The base paper for release paper according to any one of [1] to [4], wherein the inorganic pigment A is kaolin.
[6] The base paper for release paper according to any one of [1] to [5], wherein the synthetic resin latex has a glass transition temperature of -20 to 30 ° C.
[7] The base paper for release paper according to any one of [1] to [6], wherein the synthetic resin latex is a styrene-budaziene copolymer latex.
[8] The coating amount of the sealing layer determined from the basis weight difference between the base paper and the base paper for release paper measured based on JIS P 8124: 2011 under the environment of JIS P 8111: 1998 is 8 to 20 g. The base paper for release paper according to any one of [1] to [7], which is characterized by being / m 2 . [9] Described in any one of [1] to [8], wherein the surface roughness of the sealing layer surface measured based on JIS B 0601: 1994 is 0.5 to 1.0 μm. Base paper for release paper.
[10] The description according to any one of [1] to [9], wherein the air permeability resistance (Oken type testing machine method) defined in JIS P 8117: 2009 is 100,000 seconds or more. Base paper for release paper.
[11] A release paper having a release agent layer on the sealing layer of the release paper base paper according to any one of [1] to [10], and under the environment of JIS P 8111: 1998, JIS P 8124. : The release amount of the release agent layer determined from the difference in basis weight between the release paper base paper and the release paper measured based on 2011 is 0.5 to 2.0 g / m 2. paper.
[12] The release paper according to [11], wherein the release agent layer is a silicone resin layer.
In the present invention, "absolute drying" means drying at 105 ° C. for 1 to 2 hours, and hereinafter, the mass parts of the pigment and the synthetic resin latex used in the present invention are referred to as "mass parts after absolute drying". ..
本発明によれば、原紙上にポリエチレン等の樹脂をラミネートすることなく、剥離剤である溶剤系シリコーン樹脂、水系エマルジョン系シリコーン樹脂又は無溶剤系シリコーン樹脂を直接塗工することが可能である剥離紙用原紙、及び、該剥離紙用原紙に剥離剤を塗工することによって得られる、優れた密着性、剥離性、離解性を有する剥離紙を提供することができる。 According to the present invention, it is possible to directly apply a solvent-based silicone resin, a water-based emulsion-based silicone resin, or a solvent-free silicone resin as a release agent without laminating a resin such as polyethylene on the base paper. It is possible to provide a base paper for paper and a release paper having excellent adhesion, peelability, and releasability obtained by applying a release agent to the base paper for release paper.
本発明の剥離紙用原紙は、基紙の少なくとも一方の面に、少なくとも顔料成分及び接着剤成分を含有する目止め層を設けてなり、前記顔料成分としてアスペクト比が10以上である無機顔料A及びアスペクト比が10未満である無機顔料Bを含有し、前記無機顔料Aと前記無機顔料Bの配合比率が質量比で95/5〜50/50であり、前記接着剤成分が少なくとも合成樹脂ラテックスを含有すると共に、前記顔料成分の絶乾100質量部に対する該合成樹脂ラテックスの配合量が、絶乾で20〜50質量部である。 The base paper for release paper of the present invention is provided with a sealing layer containing at least a pigment component and an adhesive component on at least one surface of the base paper, and the inorganic pigment A having an aspect ratio of 10 or more as the pigment component. And an inorganic pigment B having an aspect ratio of less than 10, the blending ratio of the inorganic pigment A and the inorganic pigment B is 95/5 to 50/50 by mass, and the adhesive component is at least a synthetic resin latex. The amount of the synthetic resin latex blended with respect to 100 parts by mass of the pigment component in absolute dryness is 20 to 50 parts by mass in absolute dryness.
(基紙)
本発明において基紙とは、主としてパルプからなるシートであり、填料、各種助剤を含んでもよい。
パルプとしては、広葉樹漂白クラフトパルプ(LBKP)、針葉樹漂白クラフトパルプ(NBKP)、広葉樹未漂白クラフトパルプ(LUKP)、針葉樹未漂白パルプ(NUKP)、サルファイトパルプなどの化学パルプ、ストーングラインドパルプ、サーモメカニカルパルプ、リファイナーグラインドパルプなどの機械パルプ、脱墨パルプ、古紙パルプ、再生パルプなどの木材繊維、ケナフ、竹、麻などから得られた非木材繊維などを用いることができ、適宜配合して用いることが可能である。
(Base paper)
In the present invention, the base paper is a sheet mainly made of pulp, and may contain a filler and various auxiliaries.
Examples of pulp include broadleaf bleached kraft pulp (LBKP), coniferous bleached kraft pulp (NBKP), broadleaf unbleached kraft pulp (LUKP), coniferous unbleached kraft pulp (NUKP), chemical pulp such as sulfite pulp, stone grind pulp, and thermo. Mechanical pulp such as mechanical pulp and refiner grind pulp, wood fiber such as deinked pulp, used paper pulp and recycled pulp, and non-wood fiber obtained from kenaf, bamboo, hemp, etc. can be used, and are appropriately mixed and used. It is possible.
填料としては、ホワイトカーボン、タルク、カオリン、クレー、重質炭酸カルシウム、軽質炭酸カルシウム、酸化チタン、ゼオライト、合成樹脂填料等の公知の填料を使用することができる。また、硫酸バンドや各種のアニオン性、カチオン性、ノニオン性あるいは、両性の歩留まり向上剤、濾水性向上剤、紙力増強剤や内添サイズ剤等の抄紙用内添助剤を必要に応じて使用することができる。さらに、染料、蛍光増白剤、pH調整剤、消泡剤、ピッチコントロール剤、スライムコントロール剤等も必要に応じて添加することができる。 As the filler, known fillers such as white carbon, talc, kaolin, clay, heavy calcium carbonate, light calcium carbonate, titanium oxide, zeolite, and synthetic resin filler can be used. In addition, if necessary, a sulfate band and various anionic, cationic, nonionic, or amphoteric yield improvers, drainage improvers, paper strength enhancers, internal sizing agents, and other papermaking aids are used. Can be used. Further, dyes, fluorescent whitening agents, pH adjusting agents, defoaming agents, pitch control agents, slime control agents and the like can be added as needed.
基紙の製造(抄紙)方法は特に限定されるものではなく、公知の長網フォーマーマシン、オントップハイブリッドフォーマーマシン、ギャップフォーマーマシン、ヤンキーマシン等を用いて、酸性抄紙、中性抄紙、アルカリ抄紙方式で抄紙して基紙を製造することができる。また、基紙は1層であってもよく、2層以上の多層で構成されていてもよい。
さらに、基紙の表面を各種薬剤で処理することが可能である。使用される薬剤としては、酸化澱粉、ヒドロキシエチルエーテル化澱粉、酵素変性澱粉、ポリアクリルアミド、ポリビニルアルコール、表面サイズ剤、耐水化剤、保水剤、増粘剤、滑剤などを例示することができ、これらを単独あるいは2種類以上を混合して用いることができる。
The method for producing the base paper (papermaking) is not particularly limited, and acidic papermaking and neutral papermaking are used using a known long net former machine, on-top hybrid former machine, gap former machine, yanky machine, or the like. , The base paper can be manufactured by papermaking by the alkaline papermaking method. Further, the base paper may have one layer or may be composed of two or more layers.
Furthermore, the surface of the base paper can be treated with various chemicals. Examples of the chemicals used include oxidized starch, hydroxyethyl etherified starch, enzyme-modified starch, polyacrylamide, polyvinyl alcohol, surface sizing agents, water resistant agents, water retention agents, thickeners, lubricants, and the like. These can be used alone or in combination of two or more.
基紙の表面処理の方法は特に限定されるものではないが、ロッドメタリングサイズプレス、ポンド式サイズプレス、ゲートロールコーター、スプレーコーター、ブレードコーター、カーテンコーターなど公知の塗工装置を用いることができる。
この様にして得られる基紙としては、上質紙、中質紙、塗工紙、片艶紙、クラフト紙、片艶クラフト紙、晒クラフト紙、グラシン紙、板紙、白板紙、ライナーなどの各種公知のものが例示可能である。
The method of surface treatment of the base paper is not particularly limited, but a known coating device such as a rod metering size press, a pound type size press, a gate roll coater, a spray coater, a blade coater, or a curtain coater can be used. it can.
Various base papers obtained in this way include high-quality paper, medium-quality paper, coated paper, single-gloss paper, kraft paper, single-gloss kraft paper, bleached kraft paper, glassin paper, paperboard, white paperboard, and liner. Known ones can be exemplified.
本発明の基紙の坪量は、剥離紙用原紙または剥離紙として用いることができる坪量であればいずれでもよいが、一般的には80g/m2〜300g/m2程度であり、100g/m2〜220g/m2のものが用いられることが多い。 The basis weight of the base paper of the present invention may be any as long as the basis weight which can be used as a base paper or release paper for release paper is generally from 80g / m 2 ~300g / m 2 approximately, 100g Those of / m 2 to 220 g / m 2 are often used.
(目止め層)
本発明の目止め層が含有する顔料成分は、アスペクト比が10以上である無機顔料A及びアスペクト比が10未満である無機顔料Bを含有する。アスペクト比が10以上である無機顔料Aを目止め層に含有することにより、扁平形状による良好な目止め性が得られる。また、アスペクト比が10未満である無機顔料Bを目止め層に含有することにより、目止め層と目止め層上に設けた剥離剤層との密着性が良好となる。
なお、アスペクト比は、無機顔料の粉体粒子を電子顕微鏡で撮影し、ランダムに抽出した粒子100個について、直径を厚さで除して平均を求めた値であり、アスペクト比の値が大きい程、無機顔料の扁平度合いが大きいことになる。
(Filling layer)
The pigment component contained in the sealing layer of the present invention contains an inorganic pigment A having an aspect ratio of 10 or more and an inorganic pigment B having an aspect ratio of less than 10. By containing the inorganic pigment A having an aspect ratio of 10 or more in the sealing layer, good sealing property due to the flat shape can be obtained. Further, by containing the inorganic pigment B having an aspect ratio of less than 10 in the sealing layer, the adhesion between the sealing layer and the release agent layer provided on the sealing layer is improved.
The aspect ratio is a value obtained by photographing powder particles of an inorganic pigment with an electron microscope and dividing the diameter of 100 randomly extracted particles by the thickness to obtain an average, and the value of the aspect ratio is large. The more flat the inorganic pigment is, the greater the degree of flatness.
無機顔料Aとしては、アスペクト比が10以上であり、一般に製紙に使用されている顔料を使用することができる。具体的には、カオリン、タルク、クレー、ベントナイト、サポナイト、スティブンナイト、モンモリロナイト等を例示することが可能であり、こららの顔料を1種又は2種類以上組み合わせて使用することができる。
これらの中では、より平坦性に優れると共に、剥離性に優れた剥離紙が得られるという観点、また、剥離剤塗工液を均一に薄く塗工することが可能であると共に、剥離剤の硬化を阻害しない物質である必要があるという観点から、本発明においては、平板顔料であるカオリンを使用することが好ましい。
As the inorganic pigment A, a pigment having an aspect ratio of 10 or more and generally used for papermaking can be used. Specifically, kaolin, talc, clay, bentonite, saponite, stepnite, montmorillonite and the like can be exemplified, and one or a combination of two or more of these pigments can be used.
Among these, from the viewpoint of obtaining a release paper having excellent flatness and excellent peelability, it is possible to apply the release agent coating liquid uniformly and thinly, and the release agent is cured. In the present invention, it is preferable to use kaolin, which is a flat pigment, from the viewpoint that it needs to be a substance that does not inhibit the above.
無機顔料Bとしては、アスペクト比が10未満であり、一般に製紙に使用されている顔料を使用することができる。具体的には、重質炭酸カルシウム、軽質炭酸カルシウム、二酸化チタン、水酸化アルミニウム、シリカ等を例示することが可能であり、こららの顔料を1種又は2種類以上組み合わせて使用することができる。
これらの中では、目止め層と目止め層上に設けた剥離剤層との密着性が特に良好となるため、重質炭酸カルシウム、軽質炭酸カルシウムが好ましい。
As the inorganic pigment B, a pigment having an aspect ratio of less than 10 and generally used for papermaking can be used. Specifically, heavy calcium carbonate, light calcium carbonate, titanium dioxide, aluminum hydroxide, silica and the like can be exemplified, and one or a combination of two or more of these pigments can be used. ..
Among these, heavy calcium carbonate and light calcium carbonate are preferable because the adhesion between the sealing layer and the release agent layer provided on the sealing layer is particularly good.
前記無機顔料Bのレーザー回折/散乱法で測定した体積50%平均粒子径(D50)が0.5〜2.0μmであることが好ましい。
ここで、レーザー回折/散乱法の測定装置としては、例えば、堀場製作所社の粒子径分布測定装置「Partica」、マルバーン社の粒度分布測定装置「MASTER SIZER S」などが例示可能である。
The volume 50% average particle diameter (D50) measured by the laser diffraction / scattering method of the inorganic pigment B is preferably 0.5 to 2.0 μm.
Here, examples of the laser diffraction / scattering method measuring device include, for example, the particle size distribution measuring device “Partica” manufactured by Horiba, Ltd., and the particle size distribution measuring device “MASTER SIZERS” manufactured by Malvern.
本発明の目止め層が含有する顔料成分は、アスペクト比が10以上である無機顔料Aとアスペクト比が10未満である無機顔料Bの配合比率が質量比で95/5〜50/50である。
無機顔料Aと無機顔料Bの配合比率が質量比で95/5未満であると、目止め層と目止め層上に設けた剥離剤層との密着性が不十分となる。また、無機顔料Aと無機顔料Bの配合比率が質量比で50/50を超えると、目止め性が不十分となる。
In the pigment component contained in the sealing layer of the present invention, the blending ratio of the inorganic pigment A having an aspect ratio of 10 or more and the inorganic pigment B having an aspect ratio of less than 10 is 95/5 to 50/50 in terms of mass ratio. ..
If the blending ratio of the inorganic pigment A and the inorganic pigment B is less than 95/5 by mass, the adhesion between the sealing layer and the release agent layer provided on the sealing layer becomes insufficient. Further, if the blending ratio of the inorganic pigment A and the inorganic pigment B exceeds 50/50 by mass, the sealing property becomes insufficient.
本発明の目止め層に使用される接着剤成分に含有される合成樹脂ラテックスの配合量は、前記顔料成分100質量部に対して、20〜50質量部である。合成樹脂ラテックスの配合量は30質量部以上であることが好ましい。また、40質量部以下であることが好ましい。
前記顔料成分100質量部に対する合成樹脂ラテックスの配合量が20質量部未満であると、目止め性が劣る。また、合成樹脂ラテックスの配合量が50質量部を超えると、剥離紙の離解性が悪化するために、再生紙としての利用が難しくなる。
The blending amount of the synthetic resin latex contained in the adhesive component used for the sealing layer of the present invention is 20 to 50 parts by mass with respect to 100 parts by mass of the pigment component. The blending amount of the synthetic resin latex is preferably 30 parts by mass or more. Further, it is preferably 40 parts by mass or less.
If the blending amount of the synthetic resin latex with respect to 100 parts by mass of the pigment component is less than 20 parts by mass, the sealing property is inferior. On the other hand, if the blending amount of the synthetic resin latex exceeds 50 parts by mass, the release property of the release paper deteriorates, which makes it difficult to use it as recycled paper.
また、合成樹脂ラテックスのガラス転移温度(Tg)は−20〜30℃であることが好ましい。合成樹脂ラテックスのTgが−20℃より低いと、塗工層が柔らかくなりすぎ、キズが付きやすい等の不具合が生ずる。また、Tgが30℃を超えると、目止め層が不均一になりやすくなり、ピンホール欠陥が発生し易くなる。
合成樹脂ラテックスのTgは、合成樹脂ラテックスを130℃で30分間の前処理を行った後、走査型差動熱量計(JIS K−7122に準拠して窒素雰囲気下で10mgの試料を20℃/分で昇温)での二次転移に伴う比熱の変化をTgとして、下記計算式から求める。
(Tg)=Tg1×α1+Tg2×α2+・・・+Tgn×αn
Tg1、Tg2・・・Tgn:実測した各組成単体のTg(K)
α1、α2・・・αn:全樹脂質量に対する各組成単体の質量分率(%)
The glass transition temperature (Tg) of the synthetic resin latex is preferably -20 to 30 ° C. If the Tg of the synthetic resin latex is lower than -20 ° C, the coating layer becomes too soft, causing problems such as being easily scratched. Further, when Tg exceeds 30 ° C., the sealing layer tends to be non-uniform, and pinhole defects are likely to occur.
The Tg of the synthetic resin latex is obtained by pretreating the synthetic resin latex at 130 ° C. for 30 minutes, and then using a scanning differential calorimeter (JIS K-7122) for a 10 mg sample under a nitrogen atmosphere at 20 ° C./. The change in specific heat due to the secondary transition in (warm temperature in minutes) is calculated as Tg from the following formula.
(Tg) = Tg1 x α1 + Tg2 x α2 + ... + Tgn x αn
Tg1, Tg2 ... Tgn: Tg (K) of each actually measured composition
α1, α2 ... αn: Mass fraction (%) of each composition alone with respect to the total resin mass
また、前記合成樹脂ラテックスは、Tgの範囲が−20〜30℃であれば、1種類のみを使用しても、2種以上を併用してもよい。
本発明に使用される合成樹脂ラテックスとしては、スチレン・ブタジエン系共重合体、スチレン・アクリル系共重合体、エチレン・酢酸ビニル系共重合体、ブタジエン・メチルメタクリレート系共重合体、酢酸ビニル・ブチルアクリレート系共重合体などの各種共重合体のラテックスが挙げられるが、本発明においては、カオリンとの相溶性がよい、スチレン・ブダジエン系共重合体ラテックスを使用することが好ましい。
Further, as long as the Tg range of the synthetic resin latex is -20 to 30 ° C., only one type may be used, or two or more types may be used in combination.
The synthetic resin latex used in the present invention includes a styrene / butadiene copolymer, a styrene / acrylic copolymer, an ethylene / vinyl acetate copolymer, a butadiene / methyl methacrylate copolymer, and a vinyl acetate / butyl acetate. Although latexes of various copolymers such as acrylate-based copolymers can be mentioned, in the present invention, it is preferable to use a styrene-budaziene-based copolymer latex having good compatibility with kaolin.
また、接着剤成分として、前記合成樹脂ラテックスの他、必要に応じてデンプン、ポリビニルアルコール、アクリル樹脂等のバインダーを、適宜併用してもよい。 In addition to the synthetic resin latex, a binder such as starch, polyvinyl alcohol, or acrylic resin may be used as an adhesive component as appropriate.
本発明において、目止め層には、上記した顔料成分、接着剤成分の他、必要に応じて、分散剤、耐水化剤、潤滑剤、消泡剤、防腐剤、染料等を適宜添加してもよい。 In the present invention, in addition to the pigment component and the adhesive component described above, a dispersant, a water resistant agent, a lubricant, a defoaming agent, a preservative, a dye and the like are appropriately added to the sealing layer. May be good.
本発明において、目止め層の塗工方法については特に限定されるものではなく、公知の塗工装置及び塗工系で塗工することができる。例えば、塗工装置としてはブレードコーター、バーコーター、ロールコーター、エアナイフコーター、リバースロールコーター、カーテンコーター、グラビアコーター、スプレーコーター、サイズプレスコーター、ゲートロールコーターなどが挙げられる。また、塗工系としては、主として水を媒体とする水系塗工が好ましい。
目止め層を乾燥させる手法としては、例えば、蒸気加熱ヒーター、ガスヒーター、赤外線ヒーター、電気ヒーター、熱風加熱ヒーター、マイクロウェーブ、シリンダードライヤー等の通常の方法が用いられる。
In the present invention, the coating method of the sealing layer is not particularly limited, and coating can be performed by a known coating apparatus and coating system. For example, as a coating device, a blade coater, a bar coater, a roll coater, an air knife coater, a reverse roll coater, a curtain coater, a gravure coater, a spray coater, a size press coater, a gate roll coater and the like can be mentioned. Further, as the coating system, water-based coating mainly using water as a medium is preferable.
As a method for drying the sealing layer, for example, a usual method such as a steam heater, a gas heater, an infrared heater, an electric heater, a hot air heater, a microwave, or a cylinder dryer is used.
本発明の剥離紙用原紙における目止め層の塗工量は、乾燥重量で8〜20g/m2であることが好ましく、10〜15g/m2であることがより好ましい。
目止め層の塗工量が乾燥重量で8g/m2未満であると、均一な目止め層が得られ難くなる。また、目止め層の塗工量が20g/m2を超えると、塗工量の増加に伴う品質の向上が飽和する。
The coating amount of the sealing layer in the base paper for release paper of the present invention is preferably 8 to 20 g / m 2 and more preferably 10 to 15 g / m 2 in terms of dry weight.
If the amount of coating of the sealing layer is less than 8 g / m 2 by dry weight, it becomes difficult to obtain a uniform sealing layer. Further, when the coating amount of the sealing layer exceeds 20 g / m 2 , the improvement in quality with the increase in the coating amount is saturated.
また、前記目止め層のJIS B 0601:1994に基づいて測定した表面粗さ(中心線平均粗さ)は、0.5〜1.0μmであることが好ましく、0.6〜0.8μmであることがより好ましい。
表面粗さが0.5μm未満であると、目止め層と剥離剤層との密着性が低下する傾向が見られる。また、表面粗さが1.0μmを超えると、目止め層の均一性や剥離剤層の被覆性が低下する傾向が見られる。
The surface roughness (center line average roughness) of the sealing layer measured based on JIS B 0601: 1994 is preferably 0.5 to 1.0 μm, preferably 0.6 to 0.8 μm. More preferably.
If the surface roughness is less than 0.5 μm, the adhesion between the sealing layer and the release agent layer tends to decrease. Further, when the surface roughness exceeds 1.0 μm, the uniformity of the sealing layer and the coating property of the release agent layer tend to decrease.
本発明の剥離紙用原紙のJIS P 8117:2009に規定される透気抵抗度(王研式試験機法)は、100,000秒以上であることが好ましい。透気抵抗度が100,000秒未満であると、目止め性が低下する傾向が見られる。 The air permeability resistance (Oken type testing machine method) specified in JIS P 8117: 2009 of the base paper for release paper of the present invention is preferably 100,000 seconds or more. When the air permeation resistance is less than 100,000 seconds, the sealing property tends to decrease.
本発明の剥離紙用原紙に使用することができる剥離剤としては、例えば、シリコーン樹脂、フッ素化合物、アミノアルキド化合物、ポリエステル化合物等が挙げられる。
本発明においては、シリコーン樹脂を使用することが特に好ましい。剥離剤として使用するシリコーン樹脂としては、無溶剤系シリコーン樹脂、溶剤系シリコーン樹脂、水系エマルジョン系シリコーン樹脂及び無溶剤UV硬化型シリコーン樹脂等が挙げられる。
Examples of the release agent that can be used for the base paper for release paper of the present invention include silicone resins, fluorine compounds, aminoalkyd compounds, polyester compounds and the like.
In the present invention, it is particularly preferable to use a silicone resin. Examples of the silicone resin used as the release agent include solvent-free silicone resin, solvent-based silicone resin, aqueous emulsion-based silicone resin, solvent-free UV curable silicone resin, and the like.
本発明の剥離紙は、本発明の剥離紙用原紙の目止め層の上に、剥離剤を、好ましくは塗工量が乾燥重量で0.5〜2.0g/m2となるように塗工することによって得られる。
剥離剤の剥離用原紙への塗工方法については特に限定されるものではなく、公知の塗工装置及び塗工系で塗工することができる。例えば、塗工装置としてはブレードコーター、バーコーター、ロールコーター、エアナイフコーター、リバースロールコーター、カーテンコーター、グラビアコーター、スプレーコーター、サイズプレスコーター、ゲートロールコーターなどが挙げられる。
剥離剤層を乾燥させる手法としては、例えば、蒸気加熱ヒーター、ガスヒーター、赤外線ヒーター、電気ヒーター、熱風加熱ヒーター、マイクロウェーブ、シリンダードライヤー等の通常の方法が用いられる。
In the release paper of the present invention, a release agent is applied on the sealing layer of the base paper for release paper of the present invention so that the coating amount is preferably 0.5 to 2.0 g / m 2 by dry weight. Obtained by working.
The method of applying the release agent to the release base paper is not particularly limited, and coating can be performed using a known coating device and coating system. For example, as a coating device, a blade coater, a bar coater, a roll coater, an air knife coater, a reverse roll coater, a curtain coater, a gravure coater, a spray coater, a size press coater, a gate roll coater and the like can be mentioned.
As a method for drying the release agent layer, for example, a usual method such as a steam heater, a gas heater, an infrared heater, an electric heater, a hot air heater, a microwave, or a cylinder dryer is used.
以下に実施例を挙げて本発明を具体的に示すが、本発明はこれらによって何等限定されるものではない。また、実施例における部及び%は、特に記載がない限り、それぞれ質量部及び質量%を示す。 Hereinafter, the present invention will be specifically shown with reference to examples, but the present invention is not limited thereto. Further, unless otherwise specified, parts and% in the examples indicate parts by mass and% by mass, respectively.
(評価方法)
<無機顔料>
(1)体積50%平均粒子径(D50)
レーザー回折/散乱式粒度分布測定器(マルバーン社製、MASTER SIZER S)を用いて測定した。
(2)アスペクト比
上述の方法により測定した。
(Evaluation method)
<Inorganic pigment>
(1) Volume 50% average particle diameter (D50)
The measurement was performed using a laser diffraction / scattering type particle size distribution measuring device (MASTER SIZER S manufactured by Malvern).
(2) Aspect ratio Measured by the above method.
<剥離紙用原紙の品質評価>
(1)透気抵抗度
JIS P 8117:2009に準じた方法(王研式試験機法)により測定した。
(2)表面粗さ
小型表面粗さ形状測定機(東京精密社製、SURFCOM 130A)を使用して、JIS B 0601:1994に基づいて、目止め層塗工面の中心線平均粗さ(μm)を測定した。
(3)目止め層の均一性
染色液として、10%のオイルブルーのトルエン溶液を調製した。この染色液を目止め層の塗工面に均一に塗工し、5秒後にガーゼで拭き取った後、目止め層の欠陥(ピンホール等の抜け)を目視によって観察して評価した。評価が○、△であれば実用上問題がない。
[評価基準]
○:欠陥がなく目止めが均一
△:欠陥が若干ある
×:欠陥が多い
<Quality evaluation of base paper for release paper>
(1) Air permeation resistance Measured by a method according to JIS P 8117: 2009 (Oken type testing machine method).
(2) Surface Roughness Using a small surface roughness shape measuring machine (SURFCOM 130A manufactured by Tokyo Seimitsu Co., Ltd.), the average roughness of the center line of the sealing layer coated surface (μm) based on JIS B 0601: 1994. Was measured.
(3) Uniformity of Sealing Layer A 10% oil blue toluene solution was prepared as a dyeing solution. This dyeing solution was uniformly applied to the coated surface of the sealing layer, wiped off with gauze after 5 seconds, and then defects (missing pinholes, etc.) of the sealing layer were visually observed and evaluated. If the evaluation is ○ or △, there is no problem in practical use.
[Evaluation criteria]
◯: No defects and uniform sealing Δ: Some defects ×: Many defects
<剥離紙の品質評価>
(1)シリコーン樹脂の密着性
剥離剤層の表面を指で擦り(5kg荷重)、表面状態を評価した。評価が○、△であれば実用上問題がない。
[評価基準]
○:剥離剤層の剥がれが発生しない
△:わずかに剥離剤層の剥がれが発生する
×:剥離剤層の剥がれが発生する
(2)シリコーン樹脂の被覆性
剥離剤層の表面に赤色のマジックペン(寺西化学工業社製、製品名:マジックインキ)で線を引き、5秒後にガーゼで拭き取った後、インキの付着を目視によって観察して評価した。評価が○、△であれば実用上問題がない。
[評価基準]
○:インキが付着していない
△:わずかにインキが付着している
×:インキが付着している
(3)離解性
絶乾重量40gの剥離紙を用意し、剥離紙の濃度が0.5%となるように水に浸漬させ、パルプ離解試験機(熊谷理機工業社製、JIS P 8220に準拠)で60分間離解したときの、水中への離解の程度を評価した。評価が○、△であれば実用上問題がない。
[評価基準]
○:パルプ繊維が分散しており、離解性が良好
△:わずかにパルプ繊維の結束が残っている
×:パルプ繊維の塊やパルプ繊維の結束が残っており、離解性が不良
<Quality evaluation of release paper>
(1) Adhesion of Silicone Resin The surface of the release agent layer was rubbed with a finger (load of 5 kg) to evaluate the surface condition. If the evaluation is ○ or △, there is no problem in practical use.
[Evaluation criteria]
◯: No peeling of the release agent layer △: Slight peeling of the release agent layer occurs ×: Peeling of the release agent layer occurs (2) Silicone resin coating property A red marker pen on the surface of the release agent layer A line was drawn with (Teranishi Chemical Industry Co., Ltd., product name: Magic Ink), and after 5 seconds, it was wiped off with gauze, and then the adhesion of the ink was visually observed and evaluated. If the evaluation is ○ or △, there is no problem in practical use.
[Evaluation criteria]
◯: No ink adhered Δ: Slight ink adhered ×: Ink adhered (3) Dissociability Prepare a release paper with an absolute dry weight of 40 g, and the concentration of the release paper is 0.5. The degree of dissociation into water was evaluated when the pulp was immersed in water so as to be% and dissociated with a pulp dissociation tester (manufactured by Kumagai Riki Kogyo Co., Ltd., conforming to JIS P 8220) for 60 minutes. If the evaluation is ○ or △, there is no problem in practical use.
[Evaluation criteria]
◯: Pulp fibers are dispersed and good disintegration property △: Slight pulp fiber binding remains ×: Pulp fiber lumps and pulp fiber binding remaining and poor disintegration property
<剥離紙用原紙の作製>
(基紙の作製)
カナダ式標準ろ水度(CSF)370mlの広葉樹クラフトパルプ(LBKP)100重量部を原料パルプとした。紙力剤としてカチオン化澱粉を原料パルプ100質量部に対して0.3質量部添加し、次いで、硫酸バンドを1.5質量部添加した後、長網多筒式の抄紙機を用いて抄紙を行い、坪量120g/m2の基紙を得た。
<Making base paper for release paper>
(Preparation of base paper)
100 parts by weight of hardwood kraft pulp (LBKP) having a Canadian standard filtrate (CSF) of 370 ml was used as the raw material pulp. As a paper strength agent, 0.3 parts by mass of cationized starch was added to 100 parts by mass of the raw material pulp, then 1.5 parts by mass of a sulfuric acid band was added, and then papermaking was performed using a long net multi-cylinder paper machine. A base paper having a basis weight of 120 g / m 2 was obtained.
[実施例1]
無機顔料Aとしてカオリン(イメリス社製、商品名:KCS、アスペクト比:13、D50:4.6μm)を95質量部、無機顔料Bとして軽質炭酸カルシウム(アスペクト比:1、D50:1.0μm)を5質量部、接着剤としてスチレン・ブタジエン系共重合体ラテックス(日本A&L社製、商品名:PA0330、Tg−10℃)を絶乾で30質量部配合して、目止め層用塗工液を調製した。
[Example 1]
95 parts by mass of kaolin (manufactured by Imeris, trade name: KCS, aspect ratio: 13, D50: 4.6 μm) as the inorganic pigment A, and light calcium carbonate (aspect ratio: 1, D50: 1.0 μm) as the inorganic pigment B. 5 parts by mass, and 30 parts by mass of styrene / butadiene copolymer latex (manufactured by Japan A & L Co., Ltd., trade name: PA0330, Tg-10 ° C) as an adhesive is blended in an absolute dry state to form a coating liquid for a sealing layer. Was prepared.
次いで、ブレードコーターを用いて、上記基紙の片面に、上記目止め層用塗工液を塗工量が乾燥重量で10g/m2になるように塗工、乾燥して、剥離紙用原紙を得た。 Next, using a blade coater, the coating liquid for the sealing layer is applied to one side of the base paper so that the amount of coating is 10 g / m2 in terms of dry weight, and dried to obtain a base paper for release paper. Obtained.
[実施例2]
無機顔料Bとして重質炭酸カルシウム(竹原化学工業社製、商品名:サンライトSL−100、アスペクト比:1、D50:6.5μm)を5質量部使用した以外は、実施例1と同様の方法により、剥離紙用原紙を得た。
[Example 2]
Same as Example 1 except that 5 parts by mass of heavy calcium carbonate (manufactured by Takehara Chemical Industry Co., Ltd., trade name: Sunlight SL-100, aspect ratio: 1, D50: 6.5 μm) was used as the inorganic pigment B. By the method, a base paper for release paper was obtained.
[実施例3]
無機顔料Aとしてカオリン(イメリス社製、商品名:KCS、アスペクト比:13、D50:4.6μm)を80質量部、無機顔料Bとして軽質炭酸カルシウム(アスペクト比:1、D50:1.0μm)を20質量部使用した以外は、実施例1と同様の方法により剥離紙用原紙を得た。
[Example 3]
80 parts by mass of kaolin (manufactured by Imeris, trade name: KCS, aspect ratio: 13, D50: 4.6 μm) as the inorganic pigment A, and light calcium carbonate (aspect ratio: 1, D50: 1.0 μm) as the inorganic pigment B. A base paper for release paper was obtained by the same method as in Example 1 except that 20 parts by mass was used.
[実施例4]
無機顔料Aとしてカオリン(イメリス社製、商品名:KCS、アスペクト比:13、D50:4.6μm)を50質量部、無機顔料Bとして軽質炭酸カルシウム(アスペクト比:1、D50:1.0μm)を50質量部使用した以外は、実施例1と同様の方法により剥離紙用原紙を得た。
[Example 4]
50 parts by mass of kaolin (manufactured by Imeris, trade name: KCS, aspect ratio: 13, D50: 4.6 μm) as the inorganic pigment A, and light calcium carbonate (aspect ratio: 1, D50: 1.0 μm) as the inorganic pigment B. Was used in an amount of 50 parts by mass, and a base paper for release paper was obtained by the same method as in Example 1.
[実施例5]
接着剤としてスチレン・ブタジエン系共重合体ラテックス(日本A&L社製、商品名:PA0330、Tg−10℃)を絶乾で20質量部配合した以外は、実施例1と同様の方法により剥離紙用原紙を得た。
[Example 5]
For release paper by the same method as in Example 1 except that 20 parts by mass of styrene-butadiene copolymer latex (manufactured by Japan A & L, trade name: PA0330, Tg-10 ° C.) was blended as an adhesive by absolute drying. I got the base paper.
[実施例6]
接着剤としてスチレン・ブタジエン系共重合体ラテックス(日本A&L社製、商品名:PA0330、Tg−10℃)を絶乾で50質量部配合した以外は、実施例1と同様の方法により剥離紙用原紙を得た。
[Example 6]
For release paper by the same method as in Example 1 except that 50 parts by mass of styrene-butadiene copolymer latex (manufactured by Japan A & L, trade name: PA0330, Tg-10 ° C.) was blended as an adhesive by absolute drying. I got the base paper.
[比較例1]
無機顔料Aとしてカオリン(イメリス社製、商品名:KCS、アスペクト比:13、D50:4.6μm)を100質量部使用し、無機顔料Bを使用しない以外は、実施例1と同様の方法により剥離紙用原紙を得た。
[Comparative Example 1]
100 parts by mass of kaolin (manufactured by Imeris, trade name: KCS, aspect ratio: 13, D50: 4.6 μm) was used as the inorganic pigment A, and the same method as in Example 1 was used except that the inorganic pigment B was not used. A base paper for release paper was obtained.
[比較例2]
無機顔料Aとしてカオリン(イメリス社製、商品名:KCS、アスペクト比:13、D50:4.6μm)を40質量部、無機顔料Bとして軽質炭酸カルシウム(アスペクト比:1、D50:1.0μm)を60質量部使用した以外は、実施例1と同様の方法により剥離紙用原紙を得た。
[Comparative Example 2]
40 parts by mass of kaolin (manufactured by Imeris, trade name: KCS, aspect ratio: 13, D50: 4.6 μm) as the inorganic pigment A, and light calcium carbonate (aspect ratio: 1, D50: 1.0 μm) as the inorganic pigment B. Was used in an amount of 60 parts by mass, and a base paper for release paper was obtained by the same method as in Example 1.
[比較例3]
接着剤としてスチレン・ブタジエン系共重合体ラテックス(日本A&L社製、商品名:PA0330、Tg−10℃)を絶乾で15質量部配合した以外は、実施例1と同様の方法により剥離紙用原紙を得た。
[Comparative Example 3]
For release paper by the same method as in Example 1 except that 15 parts by mass of styrene-butadiene copolymer latex (manufactured by Japan A & L, trade name: PA0330, Tg-10 ° C.) was blended as an adhesive by absolute drying. I got the base paper.
[比較例4]
接着剤としてスチレン・ブタジエン系共重合体ラテックス(日本A&L社製、商品名:PA0330、Tg−10℃)を絶乾で55質量部配合した以外は、実施例1と同様の方法により剥離紙用原紙を得た。
[Comparative Example 4]
For release paper by the same method as in Example 1 except that 55 parts by mass of styrene-butadiene copolymer latex (manufactured by Japan A & L, trade name: PA0330, Tg-10 ° C.) was blended as an adhesive by absolute drying. I got the base paper.
実施例1〜6及び比較例1〜4で得られた剥離紙用原紙について、前述した品質評価を行った。結果を表1に示す。 The quality evaluation described above was performed on the release paper base papers obtained in Examples 1 to 6 and Comparative Examples 1 to 4. The results are shown in Table 1.
[実施例7]
<剥離紙の作製>
無溶剤型シリコーン樹脂(東レ・ダウコーニング・シリコーン社製、商品名:LTC-1053L)に触媒を2部添加し、剥離剤用塗工液とした。
次いで、RI印刷機を用いて、実施例1の剥離紙用原紙の目止め層の上に、上記剥離剤用塗工液を、塗工量が乾燥重量で1.0g/m2となるように塗工した後、乾燥機で硬化処理(130℃、10sec)を行い、剥離紙を得た。
[Example 7]
<Making release paper>
Two parts of a catalyst were added to a solvent-free silicone resin (manufactured by Toray Dow Corning Silicone Co., Ltd., trade name: LTC-1053L) to prepare a coating liquid for a release agent.
Next, using an RI printing machine, the above-mentioned release agent coating liquid was applied onto the sealing layer of the release paper base paper of Example 1 so that the amount of application was 1.0 g / m2 in terms of dry weight. After coating, a curing treatment (130 ° C., 10 sec) was performed in a dryer to obtain a release paper.
[実施例8]
実施例1の剥離紙用原紙の代わりに実施例2の剥離紙用原紙を使用した以外は、実施例7と同様の方法により剥離紙を得た。
[実施例9]
実施例1の剥離紙用原紙の代わりに実施例3の剥離紙用原紙を使用した以外は、実施例7と同様の方法により剥離紙を得た。
[実施例10]
実施例1の剥離紙用原紙の代わりに実施例4の剥離紙用原紙を使用した以外は、実施例7と同様の方法により剥離紙を得た。
[実施例11]
実施例1の剥離紙用原紙の代わりに実施例5の剥離紙用原紙を使用した以外は、実施例7と同様の方法により剥離紙を得た。
[実施例12]
実施例1の剥離紙用原紙の代わりに実施例6の剥離紙用原紙を使用した以外は、実施例7と同様の方法により剥離紙を得た。
[Example 8]
A release paper was obtained by the same method as in Example 7 except that the release paper base paper of Example 2 was used instead of the release paper base paper of Example 1.
[Example 9]
A release paper was obtained by the same method as in Example 7 except that the release paper base paper of Example 3 was used instead of the release paper base paper of Example 1.
[Example 10]
A release paper was obtained by the same method as in Example 7 except that the release paper base paper of Example 4 was used instead of the release paper base paper of Example 1.
[Example 11]
A release paper was obtained by the same method as in Example 7 except that the release paper base paper of Example 5 was used instead of the release paper base paper of Example 1.
[Example 12]
A release paper was obtained by the same method as in Example 7 except that the release paper base paper of Example 6 was used instead of the release paper base paper of Example 1.
[比較例5]
実施例1の剥離紙用原紙の代わりに比較例1の剥離紙用原紙を使用した以外は、実施例7と同様の方法により剥離紙を得た。
[比較例6]
実施例1の剥離紙用原紙の代わりに比較例2の剥離紙用原紙を使用した以外は、実施例7と同様の方法により剥離紙を得た。
[比較例7]
実施例1の剥離紙用原紙の代わりに比較例3の剥離紙用原紙を使用した以外は、実施例7と同様の方法により剥離紙を得た。
[比較例8]
実施例1の剥離紙用原紙の代わりに比較例4の剥離紙用原紙を使用した以外は、実施例7と同様の方法により剥離紙を得た。
[Comparative Example 5]
A release paper was obtained by the same method as in Example 7 except that the release paper base paper of Comparative Example 1 was used instead of the release paper base paper of Example 1.
[Comparative Example 6]
A release paper was obtained by the same method as in Example 7 except that the release paper base paper of Comparative Example 2 was used instead of the release paper base paper of Example 1.
[Comparative Example 7]
A release paper was obtained by the same method as in Example 7 except that the release paper base paper of Comparative Example 3 was used instead of the release paper base paper of Example 1.
[Comparative Example 8]
A release paper was obtained by the same method as in Example 7 except that the release paper base paper of Comparative Example 4 was used instead of the release paper base paper of Example 1.
実施例7〜12及び比較例5〜8で得られた剥離紙について、前述した品質評価を行った。結果を表2に示す。 The above-mentioned quality evaluation was performed on the release papers obtained in Examples 7 to 12 and Comparative Examples 5 to 8. The results are shown in Table 2.
実施例1〜6及び比較例1〜4の結果から、本発明の剥離紙用原紙は、目止め層の品質が良好であることが確認された。
また、実施例7〜12及び比較例5〜8の結果から、本発明の剥離紙は、密着性、剥離性、離解性が良好であることが確認された。
From the results of Examples 1 to 6 and Comparative Examples 1 to 4, it was confirmed that the base paper for release paper of the present invention had good quality of the sealing layer.
Further, from the results of Examples 7 to 12 and Comparative Examples 5 to 8, it was confirmed that the release paper of the present invention had good adhesion, peelability, and disintegration property.
Claims (12)
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Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
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JP2012136794A (en) * | 2010-12-24 | 2012-07-19 | Daio Paper Corp | Base paper for release paper |
JP2016160544A (en) * | 2015-02-27 | 2016-09-05 | 北越紀州製紙株式会社 | Base paper for process release paper and method for producing the same |
JP2016223036A (en) * | 2015-06-02 | 2016-12-28 | 日本製紙株式会社 | Base paper for release paper and release paper |
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Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
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JP2012136794A (en) * | 2010-12-24 | 2012-07-19 | Daio Paper Corp | Base paper for release paper |
JP2016160544A (en) * | 2015-02-27 | 2016-09-05 | 北越紀州製紙株式会社 | Base paper for process release paper and method for producing the same |
JP2016223036A (en) * | 2015-06-02 | 2016-12-28 | 日本製紙株式会社 | Base paper for release paper and release paper |
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