JPH087451B2 - Film suitable for electrophotographic copying - Google Patents
Film suitable for electrophotographic copyingInfo
- Publication number
- JPH087451B2 JPH087451B2 JP63281778A JP28177888A JPH087451B2 JP H087451 B2 JPH087451 B2 JP H087451B2 JP 63281778 A JP63281778 A JP 63281778A JP 28177888 A JP28177888 A JP 28177888A JP H087451 B2 JPH087451 B2 JP H087451B2
- Authority
- JP
- Japan
- Prior art keywords
- film
- mat layer
- chemical mat
- layer
- parts
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000000126 substance Substances 0.000 claims description 22
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 8
- 238000004132 cross linking Methods 0.000 claims description 8
- 239000000839 emulsion Substances 0.000 claims description 8
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 8
- 229920000877 Melamine resin Polymers 0.000 claims description 7
- 239000004640 Melamine resin Substances 0.000 claims description 6
- 239000003054 catalyst Substances 0.000 claims description 6
- 239000011256 inorganic filler Substances 0.000 claims description 6
- 229910003475 inorganic filler Inorganic materials 0.000 claims description 6
- 239000000203 mixture Substances 0.000 claims description 6
- 239000004094 surface-active agent Substances 0.000 claims description 5
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 239000003795 chemical substances by application Substances 0.000 claims description 4
- 229920003002 synthetic resin Polymers 0.000 claims description 4
- 239000000057 synthetic resin Substances 0.000 claims description 4
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 3
- 125000004429 atom Chemical group 0.000 claims description 3
- 229910052751 metal Inorganic materials 0.000 claims description 3
- 239000002184 metal Substances 0.000 claims description 3
- 239000000758 substrate Substances 0.000 claims 2
- 239000002253 acid Substances 0.000 claims 1
- 239000010408 film Substances 0.000 description 30
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 12
- 238000000576 coating method Methods 0.000 description 9
- 239000011248 coating agent Substances 0.000 description 8
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 6
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 6
- 239000007788 liquid Substances 0.000 description 6
- 238000001035 drying Methods 0.000 description 5
- 239000002245 particle Substances 0.000 description 5
- 239000000377 silicon dioxide Substances 0.000 description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
- 239000002216 antistatic agent Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 229920000728 polyester Polymers 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 3
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 3
- 235000019270 ammonium chloride Nutrition 0.000 description 3
- 229910000019 calcium carbonate Inorganic materials 0.000 description 3
- 229920006254 polymer film Polymers 0.000 description 3
- -1 polypropylene Polymers 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 239000004952 Polyamide Substances 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 229920006243 acrylic copolymer Polymers 0.000 description 2
- 229910021529 ammonia Inorganic materials 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 2
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 2
- KWGKDLIKAYFUFQ-UHFFFAOYSA-M lithium chloride Chemical compound [Li+].[Cl-] KWGKDLIKAYFUFQ-UHFFFAOYSA-M 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 229920002647 polyamide Polymers 0.000 description 2
- 239000004417 polycarbonate Substances 0.000 description 2
- 229920000515 polycarbonate Polymers 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 description 2
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 230000003746 surface roughness Effects 0.000 description 2
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 2
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 2
- JZLWSRCQCPAUDP-UHFFFAOYSA-N 1,3,5-triazine-2,4,6-triamine;urea Chemical compound NC(N)=O.NC1=NC(N)=NC(N)=N1 JZLWSRCQCPAUDP-UHFFFAOYSA-N 0.000 description 1
- CUOSYYRDANYHTL-UHFFFAOYSA-N 1,4-dioctoxy-1,4-dioxobutane-2-sulfonic acid;sodium Chemical compound [Na].CCCCCCCCOC(=O)CC(S(O)(=O)=O)C(=O)OCCCCCCCC CUOSYYRDANYHTL-UHFFFAOYSA-N 0.000 description 1
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
- 125000006539 C12 alkyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 229920002433 Vinyl chloride-vinyl acetate copolymer Polymers 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000002390 adhesive tape Substances 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- VBIXEXWLHSRNKB-UHFFFAOYSA-N ammonium oxalate Chemical compound [NH4+].[NH4+].[O-]C(=O)C([O-])=O VBIXEXWLHSRNKB-UHFFFAOYSA-N 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 238000006757 chemical reactions by type Methods 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 235000019441 ethanol Nutrition 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 229910003437 indium oxide Inorganic materials 0.000 description 1
- PJXISJQVUVHSOJ-UHFFFAOYSA-N indium(iii) oxide Chemical compound [O-2].[O-2].[O-2].[In+3].[In+3] PJXISJQVUVHSOJ-UHFFFAOYSA-N 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 239000005518 polymer electrolyte Substances 0.000 description 1
- 229920000193 polymethacrylate Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000007788 roughening Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 229920001909 styrene-acrylic polymer Polymers 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 229920006230 thermoplastic polyester resin Polymers 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 235000010215 titanium dioxide Nutrition 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G7/00—Selection of materials for use in image-receiving members, i.e. for reversal by physical contact; Manufacture thereof
- G03G7/0006—Cover layers for image-receiving members; Strippable coversheets
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Photoreceptors In Electrophotography (AREA)
- Laminated Bodies (AREA)
Description
【発明の詳細な説明】 (技術分野) 本発明は、静電方式の複写機に用いられる複写用に好
適なフィルムに関するものである。Description: TECHNICAL FIELD The present invention relates to a film suitable for copying used in an electrostatic copying machine.
(従来技術及びその問題点) 静電方式の複写機は広く普及しており、その複写用紙
としては、普通紙が一般に使用されてきた。(Prior Art and Problems Thereof) Electrostatic copying machines are widely used, and plain paper has been generally used as the copying paper.
しかし、普通紙は電気絶縁性が高く、帯電しやすいも
のであることから、帯電に起因する種々のトラブルが発
生する。例えば、給紙に際して起る重送(2枚送り)
や、複写紙をソータにより仕分ける際に起るトナー転写
後の静電気の残存に起因する仕分けトラブル等が発生す
る。However, since plain paper has high electric insulation and is easily charged, various troubles due to charging occur. For example, double feeding (two sheets feeding) that occurs when feeding paper
In addition, sorting troubles and the like occur due to static electricity remaining after toner transfer that occurs when sorting copy paper with a sorter.
従来、前記の如き帯電に起因する問題を解決するため
に、普通紙を帯電防止処理することが行われている。し
かし、このような帯電処理された用紙の場合、電子複写
工程において、帯電圧が不足して用紙上に十分な濃度の
トナーが乗らないという問題が生じ、未だ満足するもの
ではない。Conventionally, in order to solve the above-mentioned problems caused by electrification, plain paper is subjected to antistatic treatment. However, in the case of such a charged paper, there is a problem in the electronic copying process that the electrification voltage is insufficient and the toner of a sufficient density cannot be applied on the paper, which is not yet satisfactory.
(発明の課題) 本発明は、従来の電子複写用紙に見られる前記問題を
解決することをその課題とする。(Problems of the Invention) An object of the present invention is to solve the above problems found in conventional electronic copying paper.
(課題を解決するための手段) 本発明者らは、前記課題を解決するために鋭意研究を
重ねた結果、本発明を完成するに到った。(Means for Solving the Problems) The present inventors have completed the present invention as a result of intensive studies to solve the above problems.
即ち、本発明によれば、合成樹脂フィルムを基材フィ
ルムとし、その片面もしくは両面に、表面に粗面形成剤
による微細凹凸を有するケミカルマット層を形成し、該
ケミカルマット層の表面に該ケミカルマット層表面の微
細凹凸に応じた表面微細凹凸の帯電防止層を形成すると
共に該ケミカルマット層形成成分として下記(A)〜
(E)からなる組成物を用いたことを特徴とする電子写
真複写用に好適なフィルム。That is, according to the present invention, a synthetic resin film is used as a base film, and a chemical mat layer having fine irregularities due to a surface roughening agent is formed on one or both surfaces of the base film, and the chemical mat layer is formed on the surface of the chemical mat layer. An antistatic layer having surface irregularities corresponding to the fine irregularities on the surface of the mat layer is formed, and the following (A) to
A film suitable for electrophotographic copying, characterized by using a composition comprising (E).
(A)アクリル系エマルジョン (B)下式 〔式中、R1及びR2はそれぞれ同一又は異なる高級アルキ
ル基であり、X1及びX2は水素原子又は‐SO3M(M:金属原
子若しくはアンモニウムイオン)で示される基であり、
X1とX2とは同時に水素原子ではない。〕 で示されるジアルキルスルホン酸系界面活性剤 (C)メラミン樹脂 (D)架橋触媒 (E)無機質充填剤(粗面形成剤) が提供される。(A) Acrylic emulsion (B) The following formula (In the formula, R 1 and R 2 are respectively the same or different higher alkyl groups, X 1 and X 2 are hydrogen atoms or a group represented by —SO 3 M (M: metal atom or ammonium ion),
X 1 and X 2 are not hydrogen atoms at the same time. ] The dialkyl sulfonic-acid type surfactant shown by these (C) melamine resin (D) crosslinking catalyst (E) inorganic filler (rough surface forming agent) is provided.
本発明の電子写真複写用フィルムは、合成樹脂フィル
ムの片面もしくは両面に、特定なケミカルマット層を設
け、さらにその上に帯電防止層を設けた構造を有する。
この場合、必要に応じ、ケミカルマット層と基材フィル
ムとの間に高分子膜からなるアンカー層を介在させるこ
とができる。The electrophotographic copying film of the present invention has a structure in which a specific chemical matte layer is provided on one side or both sides of a synthetic resin film, and an antistatic layer is further provided thereon.
In this case, if necessary, an anchor layer made of a polymer film can be interposed between the chemical mat layer and the base film.
基材フィルムとしては、一般の高分子フィルムが用い
られる。このようなものとしては、例えば、ポリエステ
ル、ポリアミド(ナイロン)、ポリプロピレン、ポリエ
ステル、セルロースアセテート、ポリ塩化ビニル、ポリ
スチレン、ポリメタクリレート及びその共重合体、ポリ
カーボネート等が挙げられる。その厚さは特に制約され
ないが、一般的には、25μm〜250μmである。A general polymer film is used as the base film. Examples of such materials include polyester, polyamide (nylon), polypropylene, polyester, cellulose acetate, polyvinyl chloride, polystyrene, polymethacrylate and copolymers thereof, and polycarbonate. The thickness is not particularly limited, but is generally 25 μm to 250 μm.
ケミカルマット層は、下記(A)〜(E)成分からな
る組成物から形成されたものである。The chemical mat layer is formed from a composition containing the following components (A) to (E).
(A)アクリル系エマルジョン (B)下式 〔式中、R1及びR2はそれぞれ同一又は異なる高級アルキ
ル基であり、X1及びX2は水素原子又は‐SO3M(M:金属原
子若しくはアンモニウムイオン)で示される基であり、
X1とX2とは同時に水素原子ではない。〕 で示されるジアルキルスルフォン酸系界面活性剤 (C)メラミン樹脂 (D)架橋触媒 (E)無機質充填剤(粗面形成剤) 以下、前記ケミカルマット層成分(A)〜(E)につ
いて詳述する。(A) Acrylic emulsion (B) The following formula (In the formula, R 1 and R 2 are respectively the same or different higher alkyl groups, X 1 and X 2 are hydrogen atoms or a group represented by —SO 3 M (M: metal atom or ammonium ion),
X 1 and X 2 are not hydrogen atoms at the same time. ] The dialkyl sulfonic acid type surfactant shown by (C) Melamine resin (D) Crosslinking catalyst (E) Inorganic filler (rough surface forming agent) Hereinafter, the chemical mat layer components (A) to (E) will be described in detail. To do.
成分(A)(アクリル系エマルジョン) このエマルジョンを構成する主成分としては、アクリ
ルホモポリマー、酢酸ビニル‐アクリルコポリマー、ス
チレン‐アクリルコポリマー等が例示できる。イオン性
はノニオン、アニオンのいずれでもよい。また、自己架
橋型、反応型のいずれでもよい。濃度は、特に制限がな
く、広い範囲から選択することができる。液性について
は弱酸性ないし弱アルカリ性のものが好適である。Component (A) (Acrylic Emulsion) Examples of the main component constituting this emulsion include acrylic homopolymers, vinyl acetate-acrylic copolymers, styrene-acrylic copolymers and the like. The ionicity may be either nonionic or anionic. Further, it may be either a self-crosslinking type or a reaction type. The concentration is not particularly limited and can be selected from a wide range. Regarding the liquid property, weakly acidic to weakly alkaline ones are preferable.
成分(B)(ジアルキルスルホン酸系界面活性剤) 前記式(I)において、R1及びR2で示される高級アル
キル基は、C5〜C15、好ましくはC7〜C12のアルキル基で
ある。Component (B) (dialkyl sulfonic acid type surfactant) In the formula (I), the higher alkyl group represented by R 1 and R 2 is a C 5 to C 15 , preferably a C 7 to C 12 alkyl group. is there.
X1及びX2は、‐SO3M(M:Na,K,Li,NH4等)で示される
基又は水素原子であって、X1及びX2は同時に水素原子で
はなく、換言すれば、X1及びX2の少なくとも一方は‐SO
3Mで示される基であることが必要とされる。X 1 and X 2 are groups represented by —SO 3 M (M: Na, K, Li, NH 4 etc.) or a hydrogen atom, and X 1 and X 2 are not hydrogen atoms at the same time, in other words, , X 1 and X 2 are at least -SO
It is required to be a group represented by 3 M.
好適な具体例は、下記のソジウムジオクチルモノスル
フォサクシネートである。A preferred specific example is the following sodium dioctyl monosulphosuccinate.
この成分(B)は、組成物を合成樹脂フィルムに塗布
する際の該組成物に、はじき現象がみられたり、塗膜に
ピンホールが発生したりするのを防止する役目をするも
ので、塗布液の表面張力を低下させる作用を有するもの
である。 This component (B) serves to prevent the composition from being repelled when it is applied to a synthetic resin film and to prevent pinholes from appearing in the coating film. It has the effect of lowering the surface tension of the coating liquid.
成分(C)(メラミン樹脂) 従来公知の種々のものが使用できる。メラミン単独樹
脂のほかに、メラミン‐ユリア共縮合樹脂も使用でき
る。Component (C) (melamine resin) Various conventionally known compounds can be used. In addition to the melamine alone resin, a melamine-urea co-condensation resin can also be used.
成分(D)(架橋触媒) 例えば、塩化アンモニウム、しゅう酸アンモニウムが
好適である。これらは、メラミン樹脂に対して架橋触媒
として作用すると考えられる。また一部はアクリル系エ
マルジョンに対しても架橋作用を有する。例えば、塩化
アンモニウムは、加熱によりアンモニアと塩化水素に分
解し、塩化水素が架橋触媒として作用し、その後該分解
物は乾燥工程で系外に排出され、最終的に塗膜に残存す
ることはない。Component (D) (Crosslinking catalyst) For example, ammonium chloride and ammonium oxalate are suitable. It is considered that these act as a crosslinking catalyst for the melamine resin. Some of them also have a cross-linking effect on acrylic emulsions. For example, ammonium chloride is decomposed into ammonia and hydrogen chloride by heating, hydrogen chloride acts as a crosslinking catalyst, and then the decomposed product is discharged out of the system in the drying step and does not finally remain in the coating film. .
成分(E)(無機質充填剤) 例えば、天然シリカ、合成シリカ、酸化チタン、酸化
けい素、けいそう土、炭酸マグネシウム、炭酸カルシウ
ム、水酸化アルミニウム、アルミナ、タルク、クレー等
の所定粒径のものである。Ingredient (E) (inorganic filler) For example, natural silica, synthetic silica, titanium oxide, silicon oxide, diatomaceous earth, magnesium carbonate, calcium carbonate, aluminum hydroxide, alumina, talc, clay, etc. Is.
好ましい粒径は、0.1〜10μm、特に好ましくは0.5〜
5μmである。平均粒径が余り大きすぎると、筆記感が
悪くなる。また、組成物の調製時に良好な分散状態が得
られず、塗布時に塗布むらが生じる。他方、逆に余り小
さすぎると鉛筆ののりが悪くなり、筆記性に問題が生じ
る。The preferred particle size is 0.1 to 10 μm, particularly preferably 0.5 to
5 μm. If the average particle size is too large, the writing feel becomes poor. Further, a good dispersed state cannot be obtained at the time of preparation of the composition, and coating unevenness occurs at the time of coating. On the other hand, on the other hand, if it is too small, the glue on the pencil will deteriorate, and a problem will occur in writing.
本発明においては、無機質充填剤として特定のものを
選択して併用することにより所望に応じた効果を達成す
ることができる。具体的には、炭酸カルシウム、二酸化
ケイ素、酸化チタンの3種類を併用するとよい。これら
3種類の併用割合は、約6:14:1(重量比)が好適であ
る。In the present invention, a desired effect can be achieved by selecting and using a specific inorganic filler as the inorganic filler. Specifically, three kinds of calcium carbonate, silicon dioxide and titanium oxide may be used in combination. The combined ratio of these three types is preferably about 6: 14: 1 (weight ratio).
前記組成物の具体例の配合比は次のとおりである。 The compounding ratios of specific examples of the composition are as follows.
成分(A)100重量部(固型分) 成分(B)0.5〜10、好ましくは1〜5重量部 成分(C)40〜160、好ましくは80〜120重量部 成分(D)0.1〜10、好ましくは1〜5重量部 成分(E)10〜200、好ましくは80〜140重量部 本発明においては、このケミカルマット層は、その表
面にオーバーコート層として形成する帯電防止層との関
係で、中心線表面粗さが0.5〜1.3μm、好ましくは0.6
〜1.0μmになるように規定するのがよい。また、その
厚みは2〜15μm、好ましくは3〜7μmとするのがよ
い。Component (A) 100 parts by weight (solid content) Component (B) 0.5-10, preferably 1-5 parts Component (C) 40-160, preferably 80-120 parts Component (D) 0.1-10, 1 to 5 parts by weight Component (E) 10 to 200 parts by weight, preferably 80 to 140 parts by weight In the present invention, this chemical mat layer has a relationship with an antistatic layer formed as an overcoat layer on the surface thereof, Center line surface roughness 0.5-1.3 μm, preferably 0.6
It is preferable to specify the thickness to be 1.0 μm. The thickness is preferably 2 to 15 μm, more preferably 3 to 7 μm.
本発明においてケミカルマット層の上に形成する帯電
防止層は、その下面のケミカルマット層の微細凹凸に応
じた微細凹凸を表面に有するものである。このような微
細凹凸表面は、帯電防止層を薄膜とすることによって形
成される。この帯電防止層の厚さは、一般には、0.01〜
0.2μm、好ましくは0.02〜0.1μmであり、その中心線
表面粗さは、0.4〜1.2μm、好ましくは0.6〜1.0μmで
ある。帯電防止層は、前記の如き帯電防止材料を水媒体
や有機溶剤に溶解ないし分散して形成した塗布液を、ケ
ミカルマット層上に常法のコーテング法により塗布、乾
燥することによって形成される。In the present invention, the antistatic layer formed on the chemical mat layer has on its surface fine irregularities corresponding to the fine irregularities of the chemical mat layer on the lower surface thereof. Such a fine uneven surface is formed by forming the antistatic layer as a thin film. The thickness of this antistatic layer is generally from 0.01 to
0.2 μm, preferably 0.02 to 0.1 μm, and its center line surface roughness is 0.4 to 1.2 μm, preferably 0.6 to 1.0 μm. The antistatic layer is formed by applying a coating solution prepared by dissolving or dispersing the antistatic material as described above in an aqueous medium or an organic solvent onto the chemical mat layer by a conventional coating method and drying.
本発明においてケミカルマット層上に形成する帯電防
止層は、得られるフィルムの表面固有抵抗値が1×108
Ω〜1×1010Ωの範囲になるように形成すればよい。表
面固有抵抗値の調節は、塗布液中の帯電防止剤の濃度あ
るいは帯電防止層の厚さを調製することによって行うこ
とができる。In the present invention, the antistatic layer formed on the chemical mat layer has a surface resistivity value of 1 × 10 8 of the obtained film.
It may be formed in the range of Ω to 1 × 10 10 Ω. The surface specific resistance value can be adjusted by adjusting the concentration of the antistatic agent in the coating liquid or the thickness of the antistatic layer.
帯電防止層を形成するための帯電防止材料としては、
例えば、導電性の酸化第2スズ、酸化インジウム、酸化
亜鉛等の導電性金属酸化物と、ポリビニルアルコール、
スチレン‐ブタジエン共重合体、塩化ビニル‐酢酸ビニ
ル共重合体、ポリブタジエン、ポリエステル、アクリル
系共重合体等の高分子とからなるもの;塩化リチウム等
の無機塩;高分子第4級アンモニウム塩や高分子スルホ
ン酸塩等の高分子電解質等が挙げられる。As the antistatic material for forming the antistatic layer,
For example, conductive metal oxides such as conductive stannic oxide, indium oxide, and zinc oxide, polyvinyl alcohol,
Polymers such as styrene-butadiene copolymer, vinyl chloride-vinyl acetate copolymer, polybutadiene, polyester, acrylic copolymer; inorganic salts such as lithium chloride; polymeric quaternary ammonium salt and high Examples thereof include polymer electrolytes such as molecular sulfonates.
本発明の電子写真複写用フィルムにおいて、基材フィ
ルムとケミカルマット層との間に高分子膜をアンカー層
として設ける場合、その高分子としては、例えば、ポリ
エステル、ポリアミド、ポリプロピレン、ポリカーボネ
ート、ポリビニルアルコール等の熱可塑性樹脂が一般的
に用いられるが、熱硬化性樹脂や紫外線硬化性樹脂等も
使用可能である。好ましくは、熱可塑性ポリエステル樹
脂(飽和ポリエステル樹脂)が用いられ、水分散タイプ
でも溶剤可溶タイプのいずれでもよい。In the electrophotographic copying film of the present invention, when a polymer film is provided as an anchor layer between the base film and the chemical mat layer, examples of the polymer include polyester, polyamide, polypropylene, polycarbonate, polyvinyl alcohol and the like. Although the thermoplastic resin (1) is generally used, a thermosetting resin, an ultraviolet curable resin or the like can also be used. A thermoplastic polyester resin (saturated polyester resin) is preferably used, and either a water-dispersed type or a solvent-soluble type may be used.
(発明の効果) 本発明の電子写真複写用に好適なフィルムは、前記構
成であり、静電方式の複写機における複写用紙として用
いられ、従来の複写用紙に見られるような帯電に起因す
るトラブルを発生しない。また、電子複写工程において
は、十分な帯電圧を示し、複写用紙上でのトナー濃度不
足の問題を生じない。(Effect of the Invention) The film suitable for electrophotographic copying of the present invention has the above-mentioned constitution and is used as a copying paper in an electrostatic copying machine, and troubles caused by electrification as seen in the conventional copying paper. Does not occur. Further, in the electronic copying process, a sufficient charging voltage is exhibited, and the problem of insufficient toner density on the copy paper does not occur.
また、本発明のフィルムは、その表面は、微細凹凸表
面に形成されていることから、従来の普通紙と同様にす
ぐれた筆記性を有する。In addition, the film of the present invention has excellent writability similar to that of conventional plain paper because the surface of the film is formed on the surface of fine irregularities.
(実施例) 次に本発明を実施例によりさらに詳細に説明する。な
お以下において示す部及び%はいずれも重量基準であ
る。(Example) Next, the present invention will be described in more detail with reference to examples. The parts and% shown below are based on weight.
実施例、比較例 下記成分を混合して均一に分散させてケミカルマット
液を調製した。Examples and Comparative Examples The following components were mixed and uniformly dispersed to prepare a chemical mat liquid.
合成シリカ(平均粒径4μm) 5.0部 合成シリカ(平均粒径7μm) 2.0部 炭酸カルシウム(平均粒径1μm) 3.0部 チタン白 0.5部 界面活性剤溶液(表−1)参照) 6.8部 アンモニア(濃度5%水溶液) 1.4部 スチレン/アクリルエマルジョン 9.7部 アクリルエマルジョン 7.5部 水溶性メラミン樹脂 10.1部 塩化アンモニウム(20%水溶液) 1.1部 水 24.5部 得られたケミカルマット液をポリエチレンテレフタレ
ートフィルム(厚さ:38μm、50μm又は75μm)の両
面に乾燥後の膜厚が7〜8μmとなるように塗布、乾燥
した後、その上に、第4級アンモニウム塩系帯電防止剤
1.2部、メチルセロソルブ2.5部、エチルアルコール10.0
部及び水36.3部からなる帯電防止液を乾燥後の膜厚が0.
03〜0.05μm(フィルム番号I〜IV)及び5〜10μm
(フィルム番号V)となるように塗布、乾燥して電子写
真複写用フィルムを得た。Synthetic silica (average particle size 4 μm) 5.0 parts Synthetic silica (average particle size 7 μm) 2.0 parts Calcium carbonate (average particle size 1 μm) 3.0 parts Titanium white 0.5 parts Surfactant solution (see Table-1) 6.8 parts Ammonia (concentration 5% aqueous solution) 1.4 parts Styrene / acrylic emulsion 9.7 parts Acrylic emulsion 7.5 parts Water-soluble melamine resin 10.1 parts Ammonium chloride (20% aqueous solution) 1.1 parts Water 24.5 parts The obtained chemical mat liquid is a polyethylene terephthalate film (thickness: 38 μm, 50 μm or 75 μm) on both surfaces so that the film thickness after drying is 7 to 8 μm, and after drying, a quaternary ammonium salt-based antistatic agent
1.2 parts, methyl cellosolve 2.5 parts, ethyl alcohol 10.0
Of the antistatic liquid consisting of 3 parts of water and 36.3 parts of water has a thickness of 0.
03-0.05μm (Film Nos. I-IV) and 5-10μm
A film for electrophotographic copying was obtained by coating and drying so that (Film No. V) was obtained.
なお、フィルム番号I〜IVのものはケミカルマット層
表面の微細凹凸に応じた表面微細凹凸の帯電防止層が形
成されていたが、フィルム番号Vの帯電防止層はケミカ
ルマット層の微細凹凸の形状に沿ったものではなく、ケ
ミカルマット層の凹凸全面を被覆し、かつそれ自体平滑
な表面を有するものであった。これらのフィルムの特性
を次表に示す。Although the film Nos. I to IV had an antistatic layer having a surface fine unevenness corresponding to the fine unevenness on the surface of the chemical mat layer, the antistatic layer of film No. V had a shape of the fine unevenness of the chemical mat layer. However, the entire surface of the unevenness of the chemical matte layer was covered, and the surface itself had a smooth surface. The properties of these films are shown in the following table.
次に、前記で得た各フィルムについて、複写機
((株)リコー製、RICOPY FT5840)を用いて複写試験
を行い、その性能評価を以下のようにして行った。その
結果を表‐2に示す。 Next, each of the films obtained above was subjected to a copy test using a copying machine (RICOPY FT5840, manufactured by Ricoh Co., Ltd.), and its performance was evaluated as follows. The results are shown in Table-2.
(画像濃度) 複写により得られたコピーフィルムを、原稿と比べ、
濃度低下がないかどうか、トナーの一部又は全部のカケ
がないかどうかを調べた。(Image density) Compare the copy film obtained by copying with the original,
It was examined whether there was a decrease in density, and whether or not some or all of the toner was chipped.
(重送) フィルム50枚を連続してコピーした時の重送枚数を調
べた。(Double feed) The number of double feeds when 50 films were continuously copied was examined.
(トナー接着) 複写により得られたコピーフィルムの画像面に、粘着
剤テープを貼付し、引きはがした時に、そのテープに移
行した画像の度合を調べた。(Toner Adhesion) An adhesive tape was attached to the image side of the copy film obtained by copying, and when peeled off, the degree of the image transferred to the tape was examined.
フロントページの続き (56)参考文献 特開 昭57−182757(JP,A) 特開 昭57−14849(JP,A) 実開 昭58−88241(JP,U)Continuation of the front page (56) References JP-A-57-182757 (JP, A) JP-A-57-14849 (JP, A) Actually developed 58-88241 (JP, U)
Claims (1)
の片面もしくは両面に、表面に粗面形成剤による微細凹
凸を有するケミカルマット層を形成し、該ケミカルマッ
ト層の表面に該ケミカルマット層表面の微細凹凸に応じ
た表面微細凹凸の帯電防止層を形成すると共に該ケミカ
ルマット層形成成分として下記(A)〜(E)からなる
組成物を用いたことを特徴とする電子写真複写用に好適
なフィルム。 (A)アクリル系エマルジョン (B)下式 〔式中、R1及びR2はそれぞれ同一又は異なる高級アルキ
ル基であり、X1及びX2は水素原子又は‐SO3M(M:金属原
子若しくはアンモニウムイオン)で示される基であり、
X1とX2とは同時に水素原子ではない。〕 で示されるジアルキルスルホン酸系界面活性剤 (C)メラミン樹脂 (D)架橋触媒 (E)無機質充填剤(粗面形成剤)1. A synthetic resin film is used as a substrate film, and a chemical mat layer having fine irregularities on the surface is formed on one or both sides of the substrate film, and the chemical mat layer surface is formed on the surface of the chemical mat layer. Suitable for electrophotographic copying, characterized in that an antistatic layer having a surface fine unevenness corresponding to the fine unevenness is formed and a composition comprising the following (A) to (E) is used as the chemical mat layer forming component. Film. (A) Acrylic emulsion (B) The following formula (In the formula, R 1 and R 2 are respectively the same or different higher alkyl groups, X 1 and X 2 are hydrogen atoms or a group represented by —SO 3 M (M: metal atom or ammonium ion),
X 1 and X 2 are not hydrogen atoms at the same time. ] A dialkylsulfonic acid-based surfactant represented by (C) Melamine resin (D) Cross-linking catalyst (E) Inorganic filler (rough surface forming agent)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP63281778A JPH087451B2 (en) | 1988-11-07 | 1988-11-07 | Film suitable for electrophotographic copying |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP63281778A JPH087451B2 (en) | 1988-11-07 | 1988-11-07 | Film suitable for electrophotographic copying |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH02127656A JPH02127656A (en) | 1990-05-16 |
| JPH087451B2 true JPH087451B2 (en) | 1996-01-29 |
Family
ID=17643847
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP63281778A Expired - Lifetime JPH087451B2 (en) | 1988-11-07 | 1988-11-07 | Film suitable for electrophotographic copying |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH087451B2 (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4703920B2 (en) * | 2001-09-13 | 2011-06-15 | 日立化成フィルテック株式会社 | Wrap film storage case |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5714849A (en) * | 1980-06-30 | 1982-01-26 | Fuji Photo Film Co Ltd | Transfer film for electrophotographic copier |
| JPS57182757A (en) * | 1981-05-07 | 1982-11-10 | Ricoh Co Ltd | Lithography |
| JPS5888241U (en) * | 1981-12-02 | 1983-06-15 | キソ化成産業株式会社 | Electrophotographic transparent film for toner transfer |
-
1988
- 1988-11-07 JP JP63281778A patent/JPH087451B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| JPH02127656A (en) | 1990-05-16 |
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