JPS5942865B2 - transparent paper - Google Patents
transparent paperInfo
- Publication number
- JPS5942865B2 JPS5942865B2 JP8361077A JP8361077A JPS5942865B2 JP S5942865 B2 JPS5942865 B2 JP S5942865B2 JP 8361077 A JP8361077 A JP 8361077A JP 8361077 A JP8361077 A JP 8361077A JP S5942865 B2 JPS5942865 B2 JP S5942865B2
- Authority
- JP
- Japan
- Prior art keywords
- paper
- chelate
- transparent paper
- agent
- transparency
- 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
Links
- 229920000642 polymer Polymers 0.000 claims description 16
- 239000013522 chelant Substances 0.000 claims description 14
- 239000008395 clarifying agent Substances 0.000 claims description 14
- 239000003795 chemical substances by application Substances 0.000 claims description 4
- 229920006163 vinyl copolymer Polymers 0.000 claims description 4
- 238000006243 chemical reaction Methods 0.000 claims description 3
- 238000000576 coating method Methods 0.000 claims description 3
- 239000011248 coating agent Substances 0.000 claims description 2
- 239000001797 sucrose acetate isobutyrate Substances 0.000 claims description 2
- UVGUPMLLGBCFEJ-SWTLDUCYSA-N sucrose acetate isobutyrate Chemical group CC(C)C(=O)O[C@H]1[C@H](OC(=O)C(C)C)[C@@H](COC(=O)C(C)C)O[C@@]1(COC(C)=O)O[C@@H]1[C@H](OC(=O)C(C)C)[C@@H](OC(=O)C(C)C)[C@H](OC(=O)C(C)C)[C@@H](COC(C)=O)O1 UVGUPMLLGBCFEJ-SWTLDUCYSA-N 0.000 claims description 2
- 235000010983 sucrose acetate isobutyrate Nutrition 0.000 claims description 2
- 238000000034 method Methods 0.000 description 11
- 239000000203 mixture Substances 0.000 description 9
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 4
- 229920001577 copolymer Polymers 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- 229910000679 solder Inorganic materials 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 229920001187 thermosetting polymer Polymers 0.000 description 4
- 239000004925 Acrylic resin Substances 0.000 description 3
- 229920000178 Acrylic resin Polymers 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- QXNIBPDSSDVBQP-UHFFFAOYSA-N acetic acid;2-methylpropanoic acid Chemical compound CC(O)=O.CC(C)C(O)=O QXNIBPDSSDVBQP-UHFFFAOYSA-N 0.000 description 3
- 238000011109 contamination Methods 0.000 description 3
- 238000001723 curing Methods 0.000 description 3
- 230000006866 deterioration Effects 0.000 description 3
- 238000005470 impregnation Methods 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 150000003384 small molecules Chemical class 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 description 2
- 229920000297 Rayon Polymers 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- YRKCREAYFQTBPV-UHFFFAOYSA-N acetylacetone Chemical compound CC(=O)CC(C)=O YRKCREAYFQTBPV-UHFFFAOYSA-N 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 229920003180 amino resin Polymers 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- 239000001913 cellulose Substances 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000003822 epoxy resin Substances 0.000 description 2
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 229920000647 polyepoxide Polymers 0.000 description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 description 2
- 238000010186 staining Methods 0.000 description 2
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 2
- 229920005992 thermoplastic resin Polymers 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
- CUSMSMHSBMMCNS-UHFFFAOYSA-N 3-acetyl-5-methylhex-5-ene-2,4-dione Chemical compound CC(=O)C(C(C)=O)C(=O)C(C)=C CUSMSMHSBMMCNS-UHFFFAOYSA-N 0.000 description 1
- 239000004342 Benzoyl peroxide Substances 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 229920003043 Cellulose fiber Polymers 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical class OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 description 1
- GKKZMYDNDDMXSE-UHFFFAOYSA-N Ethyl 3-oxo-3-phenylpropanoate Chemical compound CCOC(=O)CC(=O)C1=CC=CC=C1 GKKZMYDNDDMXSE-UHFFFAOYSA-N 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- 241000220317 Rosa Species 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 235000010724 Wisteria floribunda Nutrition 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- SMZOGRDCAXLAAR-UHFFFAOYSA-N aluminium isopropoxide Chemical compound [Al+3].CC(C)[O-].CC(C)[O-].CC(C)[O-] SMZOGRDCAXLAAR-UHFFFAOYSA-N 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 239000012752 auxiliary agent Substances 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 238000010009 beating Methods 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 239000002738 chelating agent Substances 0.000 description 1
- DZMJPYGBKWJZIR-UHFFFAOYSA-N chloroethene;styrene Chemical compound ClC=C.C=CC1=CC=CC=C1 DZMJPYGBKWJZIR-UHFFFAOYSA-N 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- GPLRAVKSCUXZTP-UHFFFAOYSA-N diglycerol Chemical compound OCC(O)COCC(O)CO GPLRAVKSCUXZTP-UHFFFAOYSA-N 0.000 description 1
- XYIBRDXRRQCHLP-UHFFFAOYSA-N ethyl acetoacetate Chemical compound CCOC(=O)CC(C)=O XYIBRDXRRQCHLP-UHFFFAOYSA-N 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 238000010559 graft polymerization reaction Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 125000005395 methacrylic acid group Chemical group 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- 238000013008 moisture curing Methods 0.000 description 1
- 239000006082 mold release agent Substances 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 229920001083 polybutene Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 230000001376 precipitating effect Effects 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 238000007127 saponification reaction Methods 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 238000005809 transesterification reaction Methods 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000011345 viscous material Substances 0.000 description 1
- 230000002087 whitening effect Effects 0.000 description 1
Landscapes
- Paper (AREA)
Description
【発明の詳細な説明】
本発明は、静電式複写機を用いて、画像を形成する第2
原図用紙に関するものであり、更に詳しくは耐熱性に優
れ、加熱定着時における搬送性の良好な第2原図用紙に
関するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention provides a second method for forming an image using an electrostatic copying machine.
The present invention relates to an original paper, and more specifically, to a second original paper that has excellent heat resistance and good transportability during heat fixing.
従来この用途に使用されている用紙は、セルロースパル
プを高度に粘状叩解して抄造したトレーシングペーパー
、もしくは比較的不透明な紙に油状物質、ポリブテン等
の比較的軟化点の低い樹脂、アルカノール変性アミノ樹
脂などの熱硬化性物質等を含浸処理したものである。Conventionally, the paper used for this purpose is tracing paper made by beating cellulose pulp to a highly viscous state, or relatively opaque paper containing oily substances, resins with relatively low softening points such as polybutene, and alkanol-modified paper. It is impregnated with a thermosetting substance such as amino resin.
ところでトレーシングペーパーは最も広く使用されてい
るが、湿度にきわめて敏感なため、寸法安定性が悪くカ
ール等を起し易い。By the way, tracing paper is the most widely used paper, but it is extremely sensitive to humidity, has poor dimensional stability, and is prone to curling.
さらに熱定着に弱い上に耐水性や引裂強度などに欠点が
多い。一方油状物質、軟化点の低い熱可塑性樹脂を透明
化剤として含浸させた第2原図用紙は、それらの欠点は
ないが熱定着ロールまたは加圧定着ロールを汚す欠点が
ある。また透明化剤のマイグレーションが起り易い上に
折り目がつき易い等の欠点が多い。更に軟化点の高い熱
可塑性樹脂を用いても、耐熱性は充分でなく粘看力が強
いため逆に用紙が定着ロールに巻き付きジャム(つまつ
て動かなくなる現象)を起し、搬送性が極端に悪化する
。アルカノール変性アミノ樹脂は、熱定着時にホルマリ
ンが発生するために、乾式静電複写機には適当ではない
。本発明者等は、これ等の欠点を改良するために、各種
の透明化剤につき検討を行なつた結果、キレート反応に
よりポリマーの橋かけを行なうビニル系共重合体を用い
ると、熱定着性に優れ、搬送性の非常に良好な第2原図
用紙が得られることを見いだした。Furthermore, it is weak in heat fixing and has many drawbacks in water resistance and tear strength. On the other hand, the second original paper impregnated with an oily substance or a thermoplastic resin with a low softening point as a transparency agent does not have these disadvantages, but has the disadvantage of staining the heat fixing roll or the pressure fixing roll. Moreover, it has many disadvantages such as easy migration of the transparentizing agent and easy formation of creases. Furthermore, even if a thermoplastic resin with a high softening point is used, it does not have sufficient heat resistance and has a strong adhesive force, which can cause the paper to wrap around the fixing roll and cause jams (a phenomenon in which it gets stuck and does not move), resulting in extremely poor conveyance. worsens. Alkanol-modified amino resins are not suitable for dry electrostatic copying machines because they generate formalin during heat fixing. In order to improve these drawbacks, the present inventors investigated various clarifying agents, and found that when using a vinyl copolymer that cross-links polymers through a chelate reaction, heat fixability is improved. It has been found that a second original paper sheet with excellent transportability and excellent transportability can be obtained.
即ち、透明化剤ポリマーの一部分に錯生成のできる部分
をとり入れ、これに金属を導入することによつて分子間
橋かけを形成して高分子化、耐熱性の向上をはかること
ができる。That is, by incorporating a part that can form a complex into a part of the clarifying agent polymer and introducing a metal into it, it is possible to form intermolecular bridges, thereby increasing the polymerization and improving heat resistance.
高分子キレート生成に用いられる配位基のおもなものを
あげると次のとおりであり、これ等をアクリル酸エステ
ル、メタクリル酸エステル、スチレン塩化ビニル、酢酸
ビニル等のビニル系共重合体中に導入すればよい。The main coordination groups used in polymer chelate formation are as follows, and these are incorporated into vinyl copolymers such as acrylic esters, methacrylic esters, styrene vinyl chloride, and vinyl acetate. Just introduce it.
配位基としては例えば 等である。Examples of coordination groups include etc.
またキレートを形成する金属はほとんどあらゆる金属に
およんでいるが代表的なものは亜鉛、鉄、ニツケル、コ
バルト、銅、カルシウム、バリウム、マンガン、アルミ
ニウム、リチウム、ナトリウム等である。The metals that form chelates include almost all kinds of metals, but typical ones include zinc, iron, nickel, cobalt, copper, calcium, barium, manganese, aluminum, lithium, and sodium.
分子中に配位基を導入する方法は特に限定されるもので
はなく、例えばポリビニルアルコールの如く先に重合体
を形成したのちにエステル交換反応により下記の如き配
位基を導入する方法、またはおよび
の如き配位基含有モノマーを直接共重合、グラフト重合
することによつて得る方法などがある。The method of introducing the coordination group into the molecule is not particularly limited, and for example, a method of first forming a polymer such as polyvinyl alcohol and then introducing the following coordination group by transesterification, or There are methods such as direct copolymerization or graft polymerization of coordination group-containing monomers such as.
更に驚くべきことは、これらキレート高分子は単独でも
比較的透明性が良好であるがーー層透明性を改良するた
めに、分子量2000以下の液状ないし低融点である低
分子量化合物を多量にブレンドした場合にも耐熱性が悪
くならず、優れた透明性と搬送性を示すことである。こ
れらブレンド化合物としては、例えばシユークローズア
セテートイソブチレート(分子量845、粘看性物質)
、ポリプロピレングリコールグリセリルエーテル、低分
子量透明化剤(ビステツクスΦ141中京油脂KK製)
等がある。ただし、これ等の低分子量化合物は、品種に
よつてはキレート高分子と等量以上混合した際には急激
に耐熱性の劣化を招くから注意が必要である。等量以下
の場合には耐熱性の劣化は殆で認められなかつた。更に
低分子量化合物を主たる透明化剤として用いた場合に認
められる折り目のつき易さも発生せず、強く折り曲げて
も全く白化は認められなかつた。これらはキレート剤が
セルロース繊維にも作用してセルロースと強固に結合す
るためではないかと思われる。なお上記組成の他に、必
要に応じて帯電防止剤、着色剤、離型剤等の助剤を適宜
添加することも有効である。本発明において上記透明化
剤組成物を紙に含浸する方法は、特に限定されるもので
はなく、デイツプスクイズ方式、ロールコート方式、エ
アナイフ方式、ワイアバー方式等いずれの方式も可能で
ある。What is even more surprising is that these chelate polymers have relatively good transparency when used alone; however, in order to improve the layer transparency, a large amount of a low molecular weight compound with a molecular weight of 2000 or less and a liquid or low melting point was blended. Even in cases where heat resistance is not deteriorated, it exhibits excellent transparency and transportability. These blend compounds include, for example, seurose acetate isobutyrate (molecular weight 845, viscous substance)
, polypropylene glycol glyceryl ether, low molecular weight clarifying agent (Vistex Φ141 manufactured by Chukyo Yushi KK)
etc. However, depending on the product type, these low molecular weight compounds must be used with caution because when mixed with the chelate polymer in an equal or greater amount, the heat resistance will rapidly deteriorate. When the amount was less than the same amount, almost no deterioration in heat resistance was observed. Furthermore, the tendency to crease, which is observed when a low molecular weight compound is used as the main clarifying agent, did not occur, and no whitening was observed even when it was strongly bent. This seems to be because the chelating agent also acts on the cellulose fibers and forms a strong bond with the cellulose. In addition to the above composition, it is also effective to appropriately add auxiliary agents such as antistatic agents, colorants, and mold release agents, if necessary. In the present invention, the method for impregnating paper with the above-mentioned clarifying agent composition is not particularly limited, and any method such as a deep squeeze method, a roll coating method, an air knife method, a wire bar method, etc. can be used.
含浸量は目的とする透明性の程度によつて、原紙に対し
5〜80重量%が適当であり、含浸量が増すに従つて透
明性は向上する。この際含浸量が増しても、他の透明化
剤において見られるような定看ロールの汚染、搬送性の
劣化をひき起こさない特長を有している。塗布後の乾燥
も単に溶媒が除去されれば良く、塗布後のキユアリング
等の操作も必要ないため、ドライヤー内で速やかに乾燥
されるため、処理のスピードを高めることができ経済的
である。The amount of impregnation is suitably 5 to 80% by weight based on the base paper depending on the desired degree of transparency, and the transparency improves as the amount of impregnation increases. In this case, even if the amount of impregnation increases, it has the advantage that it does not cause contamination of the fixed roll or deterioration of conveyance properties as seen with other clarifying agents. Drying after application requires only that the solvent be removed, and there is no need for operations such as curing after application, so the process can be quickly dried in a dryer, which is economical as it can speed up the process.
更に本発明の透明化剤の特徴は、ポツトライフに制限が
無いため、二液性及び一液性のウレタン樹脂、エポキシ
樹脂の如く、製造上の制約が無くこの面でも非常に生産
性の良いことである。即ち二液性のウレタンは勿論のこ
と一液性の硬化型ウレタン樹脂(湿気硬化タイプ)は実
質上数時間単位のライフしかなく、製造工程上煩雑な因
子が増大し、製造中に樹脂液がゲル化するという危険に
常にさらされている。エポキシ樹脂その他の熱硬化性樹
脂においても、塗工機の乾燥器内で実質的にキユアリン
グを完了するように硬化速度を速めた液は同様に数時間
のポツトライフしか確保できないのが実情である。以上
本件発明の多数の特長を述べてきたが、以下更に実施例
により具体的に説明する。Another feature of the clarifying agent of the present invention is that there is no limit to the pot life, so unlike two-component and one-component urethane resins and epoxy resins, there are no manufacturing restrictions and it is extremely productive in this respect. It is. In other words, not only two-component urethane but also one-component curable urethane resin (moisture curing type) has a lifespan of only a few hours, which increases the complexity of the manufacturing process, and the resin liquid leaks during manufacturing. It is always in danger of gelling. In the case of epoxy resins and other thermosetting resins, the actual situation is that liquids whose curing speed has been increased to substantially complete curing in the dryer of a coating machine can only have a pot life of several hours. A number of features of the present invention have been described above, and will be explained in more detail below with reference to Examples.
実施例 1
NBKP20部、LBKP8O部から成るパルプを33
2SRに叩解して抄紙した米坪49めろ成ハンダ一透明
度34%の無サイズ紙に、サーモラツクST−105(
綜研化学社製 アクリル系キレート高分子)のトルエン
酢エチ30%溶液を含浸し、固形分99/m゛付看させ
乾燥した。Example 1 Pulp consisting of 20 parts of NBKP and 80 parts of LBKP was
Thermorak ST-105 (
It was impregnated with a 30% solution of acrylic chelate polymer (manufactured by Soken Kagaku Co., Ltd.) in toluene and ethyl acetate, and dried to a solid content of 99/m2.
得られた透明紙のハンダ一透明度は48%であつた。The solder transparency of the obtained transparent paper was 48%.
この透明紙は耐熱性が非常に良好であり、鏡面金属板間
にはさんで18『Cにてホツトプレスしたところ、透明
紙同志のプロツキングが無い上に鏡面板の汚染も全く認
められなかつtら更にゼロツクス2400型乾式静電式
複写機(富士ゼロツクス社製品)にて画像を複製したと
ころ、定看ロール部(温度19『C)へのトナーのオフ
セツト、透明化剤によるロール汚染が全く無く、5,0
00枚通紙しても、搬送トラブルは全く発生しなかつた
。This transparent paper has very good heat resistance, and when it was sandwiched between mirror-finished metal plates and hot pressed at 18"C, there was no blocking between the transparent papers and no contamination of the mirror-finished plates was observed. Furthermore, when the image was reproduced using a Xerox 2400 dry electrostatic copying machine (manufactured by Fuji Xerox Co., Ltd.), there was no toner offset to the regular roll section (temperature 19°C) and no roll contamination by the clarifying agent. 5,0
Even after passing 00 sheets, no conveyance trouble occurred.
一方、比較のために、透明化剤として、熱可塑性アクリ
ル樹脂(三菱レーヨン社製 ダイヤナールLR−469
軟化温度80ンC)、・熱硬化性アクリル樹脂(三菱レ
ーヨン社製 ジユラクロンRE−377、及び大日本イ
ンキ社製 アクリデイツクA−810)を用いて実施例
1と同様にして調製した透明紙の物性は表1の如くであ
つた。On the other hand, for comparison, a thermoplastic acrylic resin (Dyanal LR-469 manufactured by Mitsubishi Rayon Co., Ltd.) was used as a clarifying agent.
Physical properties of transparent paper prepared in the same manner as in Example 1 using thermosetting acrylic resins (Dyuraclone RE-377, manufactured by Mitsubishi Rayon Co., Ltd., and Acridik A-810, manufactured by Dainippon Ink Co., Ltd.) were as shown in Table 1.
これより、本発明による透明紙は、透明性の良い上に、
通紙時の搬送性が非常に優れていることがわかる〇実施
例 2
NBKP10部、LBKP9O部から成るパルプを37
SRに叩解して抄紙した米坪559/くハンダ一透明度
3070の無サイズ上質紙に、サーモラツクST−10
5(綜研化学製アクリル系キレート高分子)とシユーク
ローズアセテートイソブチレートの混合溶液(固形分濃
度35%)を表2に示す比率で、乾燥重量79/Rrl
になるよう塗布含浸した。From this, the transparent paper according to the present invention not only has good transparency, but also
It can be seen that the conveyance property during paper passing is very excellent. Example 2 Pulp consisting of 10 parts of NBKP and 90 parts of LBKP was
Thermorack ST-10 is used on sizeless high-quality paper with a transparency of 3070 and a solder weight of 559 m2, which is beaten to SR and made into paper.
5 (acrylic chelate polymer manufactured by Soken Chemical Co., Ltd.) and a mixed solution of sucrose acetate isobutyrate (solid content concentration 35%) at the ratio shown in Table 2, dry weight 79/Rrl
It was coated and impregnated.
得られた透明紙の物性を表2に示す。Table 2 shows the physical properties of the obtained transparent paper.
表2に示される如く、透明性を一層改善する目的で、低
分子量粘看性の透明化剤をブレンドした場合でも、耐熱
性の劣化が予期に反して非常に少なく、透明性が非常に
優れているにもかかわらず、乾式静電式複写機における
搬送性の極めて良好な透明紙を得ることが出来た。As shown in Table 2, even when a low-molecular-weight viscosity clarifying agent was blended with the aim of further improving transparency, the deterioration of heat resistance was unexpectedly small and the transparency was excellent. Despite this, it was possible to obtain transparent paper that has extremely good transportability in a dry electrostatic copying machine.
試みに、普通の熱硬化性アクリル樹脂であるデユラクロ
ンRE−377単独及びRE−377とシユータローズ
アセテートイソブチレートの80/20ブレンド物を透
明化剤として実施例2と同様にして調製した透明紙で、
ハンダ一透明度38%及び41%のものは、ゼロツクス
2400型複写機による通紙テストでは、180枚目(
ジユラクロン単独)、及び2枚目(ブレンド物)に夫々
ジヤムを発生し、シェークロースアセテートイソブチレ
ートのブレンドによるシートの搬送性の劣化が著しかつ
た。As an experiment, transparent resins were prepared in the same manner as in Example 2 using a common thermosetting acrylic resin, Duracron RE-377 alone, and an 80/20 blend of RE-377 and Schutrose acetate isobutyrate as clarifying agents. with paper,
Solder with transparency of 38% and 41% was tested on the 180th sheet (
Jamming occurred in both the diyuraclone (alone) and the second sheet (blend), and the conveyance properties of the sheet were significantly deteriorated due to the shake rose acetate isobutyrate blend.
実施例 3
909のポリビニルアルコール(ケン化度75%)を4
009のエチルベンゾイルアセテートと混合し、この混
合物をメカニカルスターラ一、温度計コンデンサー付き
の11の3つロフラスコ中に入れ加熱する。Example 3 909 polyvinyl alcohol (saponification degree 75%)
Mix with ethyl benzoyl acetate of 009 and heat the mixture in a 11 three-hole flask equipped with a mechanical stirrer and a thermometer condenser.
この混合物は、オイルバス中にて36m1の蒸留液が得
られる迄、150〜170゜Cに加熱し、出来たゲル状
物は、エタノール、水、アセトンで抽出して精製した後
、ジメチルホルムアミドに溶解する。このビニルアルコ
ール・ビニルベンゾイルアセテート共重合体はアルミニ
ウムとキレートを形成する。得られたキレート高分子(
35%固形分濃度)を539/7TIの上質紙に含浸乾
燥させて99/m”付看させ1ら得られた透明紙はハン
ダ一透明度45%であり実施例1と同様に耐熱性が非常
に良好で、BM型乾式静電式複写機(IBM社製品)に
てコピーをとつたところ、トナーの定看ロールへのオフ
セツト、透明化剤による定看ロールの汚れは全く無く、
5,000枚の通紙においても搬送トラブルは皆無であ
つz実施例 4
100θのメタクリルアセチルアセトンと9009のメ
チルメタクリレートを0.3%過酸化ベンゾィルの存在
下、密栓容器中にて100℃で12時間バルク共重合さ
せる。This mixture was heated to 150-170°C in an oil bath until 36 ml of distillate was obtained, and the resulting gel was purified by extraction with ethanol, water, and acetone, and then dissolved in dimethylformamide. dissolve. This vinyl alcohol/vinyl benzoyl acetate copolymer forms a chelate with aluminum. The obtained chelate polymer (
The transparent paper obtained by impregnating and drying 539/7TI high-quality paper with 35% solids concentration and attaching it to 99/m" had a solder transparency of 45% and, as in Example 1, was extremely heat resistant. When copies were made using a BM type dry electrostatic copying machine (manufactured by IBM), there was no toner offset to the viewing roll, and there was no staining of the viewing roll due to the clarifying agent.
There was no transport trouble even when 5,000 sheets were fed.Example 4 Methacryl acetylacetone of 100θ and methyl methacrylate of 9009 were mixed in a sealed container at 100°C for 12 hours in the presence of 0.3% benzoyl peroxide. Bulk copolymerize.
得られた生成物をベンゼンに溶解し、メタノールで沈澱
させ精製した。このメチルメタクリレート・メタクリル
アセチルアセトン共重合体は亜鉛とキレートを形成する
。得られたキレート高分子を用いて実施例3と同様にし
て透明紙を製作したところ、実施例3と同じく耐熱性が
良好で、BM型複写機にて5,000枚通紙しても搬送
トラブルは発生しなかつた。実施例 5
メチルメタアクリレートJモV音臥 n−ブチルメタアク
リレート80部、スチレン10部、アクリル酸3部、イ
タコン酸2部をイソプロピルアルコール中にて還流下に
重合させ、分子量(平均)7000の共重合体を得た。The obtained product was purified by dissolving it in benzene and precipitating it with methanol. This methyl methacrylate/methacrylacetylacetone copolymer forms a chelate with zinc. Transparent paper was produced using the obtained chelate polymer in the same manner as in Example 3, and it had good heat resistance as in Example 3, and could be transported even when 5,000 sheets were passed through a BM type copying machine. No troubles occurred. Example 5 Methyl methacrylate JMoV Sound 80 parts of n-butyl methacrylate, 10 parts of styrene, 3 parts of acrylic acid, and 2 parts of itaconic acid were polymerized in isopropyl alcohol under reflux to obtain a polymer with a molecular weight (average) of 7,000. A copolymer was obtained.
上記共重合体100部(固形分比)、架橋剤トリイソプ
ロポキシアルミニウム5部、安定剤アセチルアセトン3
部、アセト酢酸エチル2部を混合し、トルエン・MEK
にて35%濃度の溶液とし、実施例2と同一の原紙に乾
燥重量89/dになるよう含浸した。100 parts of the above copolymer (solid content ratio), 5 parts of triisopropoxyaluminum as a crosslinking agent, 3 parts of acetylacetone as a stabilizer
1 part, 2 parts of ethyl acetoacetate, and toluene/MEK.
A solution with a concentration of 35% was prepared, and the same base paper as in Example 2 was impregnated with the solution to a dry weight of 89/d.
Claims (1)
ル系共重合体からなるキレート高分子を主成分とする透
明化剤を紙に対し5〜80%塗布又は含浸して成る透明
紙。 2 キレート反応によりポリマーの橋かけを行なうビニ
ル系共重合体からなるキレート高分子と共に該重合体と
等量以下(重量比)の低分子量透明化剤を混合して成る
透明化剤を紙に対し5〜80%塗布又は含浸して成る透
明紙。 3 低分子量透明化剤がシュークローズアセテートイソ
ブチレートである事を特徴とする特許請求の範囲第2項
の透明紙。[Scope of Claims] 1. Transparent paper made by coating or impregnating paper with 5 to 80% of a transparency agent whose main component is a chelate polymer made of a vinyl copolymer that crosslinks polymers through a chelate reaction. . 2. A transparentizing agent made by mixing a chelate polymer made of a vinyl copolymer that crosslinks polymers through a chelate reaction with a low molecular weight clarifying agent in an amount equal to or less than the weight ratio of the polymer is applied to the paper. Transparent paper coated or impregnated with 5 to 80%. 3. The transparent paper according to claim 2, wherein the low molecular weight clarifying agent is sucrose acetate isobutyrate.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP8361077A JPS5942865B2 (en) | 1977-07-14 | 1977-07-14 | transparent paper |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP8361077A JPS5942865B2 (en) | 1977-07-14 | 1977-07-14 | transparent paper |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5418913A JPS5418913A (en) | 1979-02-13 |
| JPS5942865B2 true JPS5942865B2 (en) | 1984-10-18 |
Family
ID=13807246
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP8361077A Expired JPS5942865B2 (en) | 1977-07-14 | 1977-07-14 | transparent paper |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5942865B2 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0633665U (en) * | 1992-10-05 | 1994-05-06 | 喜太郎 伊藤 | Offset driver |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6131213A (en) * | 1984-07-23 | 1986-02-13 | Yuuhoo Chem Kk | Composition of mold lubricant |
| JPH0825692B2 (en) * | 1992-06-30 | 1996-03-13 | 株式会社不二鉄工所 | Winding core in web winding machine |
-
1977
- 1977-07-14 JP JP8361077A patent/JPS5942865B2/en not_active Expired
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0633665U (en) * | 1992-10-05 | 1994-05-06 | 喜太郎 伊藤 | Offset driver |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5418913A (en) | 1979-02-13 |
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