JPH03167397A - Transfer paper for electrophotography - Google Patents
Transfer paper for electrophotographyInfo
- Publication number
- JPH03167397A JPH03167397A JP30822889A JP30822889A JPH03167397A JP H03167397 A JPH03167397 A JP H03167397A JP 30822889 A JP30822889 A JP 30822889A JP 30822889 A JP30822889 A JP 30822889A JP H03167397 A JPH03167397 A JP H03167397A
- Authority
- JP
- Japan
- Prior art keywords
- transfer paper
- paper
- sizing agent
- acid
- water
- 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.)
- Granted
Links
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 22
- 150000003839 salts Chemical class 0.000 claims abstract description 22
- 239000000178 monomer Substances 0.000 claims abstract description 21
- 238000004513 sizing Methods 0.000 claims abstract description 21
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims abstract description 17
- 229920001577 copolymer Polymers 0.000 claims abstract description 12
- 239000000945 filler Substances 0.000 claims abstract description 9
- 229910000019 calcium carbonate Inorganic materials 0.000 claims abstract description 8
- 125000002947 alkylene group Chemical group 0.000 claims abstract description 5
- 239000000835 fiber Substances 0.000 claims abstract description 4
- IUMRWGYGZHKZKF-UHFFFAOYSA-N 2-aminoprop-2-enamide Chemical compound NC(=C)C(N)=O IUMRWGYGZHKZKF-UHFFFAOYSA-N 0.000 claims abstract description 3
- 150000003440 styrenes Chemical class 0.000 claims abstract description 3
- 239000002253 acid Substances 0.000 claims description 10
- 239000000126 substance Substances 0.000 claims description 4
- 239000000470 constituent Substances 0.000 claims description 3
- -1 aminoalkyl ester Chemical class 0.000 abstract description 15
- 125000000217 alkyl group Chemical group 0.000 abstract description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract description 2
- 150000001408 amides Chemical class 0.000 abstract 2
- 150000002148 esters Chemical class 0.000 abstract 2
- 239000004615 ingredient Substances 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 description 10
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 7
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Natural products C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 6
- 230000000694 effects Effects 0.000 description 5
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- JKNCOURZONDCGV-UHFFFAOYSA-N 2-(dimethylamino)ethyl 2-methylprop-2-enoate Chemical compound CN(C)CCOC(=O)C(C)=C JKNCOURZONDCGV-UHFFFAOYSA-N 0.000 description 2
- 241000238557 Decapoda Species 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- NEHMKBQYUWJMIP-UHFFFAOYSA-N chloromethane Chemical compound ClC NEHMKBQYUWJMIP-UHFFFAOYSA-N 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 125000004985 dialkyl amino alkyl group Chemical group 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 230000007935 neutral effect Effects 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- 230000003068 static effect Effects 0.000 description 2
- 229940014800 succinic anhydride Drugs 0.000 description 2
- HMLSBRLVTDLLOI-UHFFFAOYSA-N 1-(dimethylamino)ethyl 2-methylprop-2-enoate Chemical compound CN(C)C(C)OC(=O)C(C)=C HMLSBRLVTDLLOI-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- SJIXRGNQPBQWMK-UHFFFAOYSA-N DEAEMA Natural products CCN(CC)CCOC(=O)C(C)=C SJIXRGNQPBQWMK-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 235000011054 acetic acid Nutrition 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000001350 alkyl halides Chemical class 0.000 description 1
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- XENVCRGQTABGKY-ZHACJKMWSA-N chlorohydrin Chemical compound CC#CC#CC#CC#C\C=C\C(Cl)CO XENVCRGQTABGKY-ZHACJKMWSA-N 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000006258 conductive agent Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000003795 desorption Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- DJLHXXNSHHGFLB-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate;n-methylmethanamine Chemical compound CNC.CCOC(=O)C(C)=C DJLHXXNSHHGFLB-UHFFFAOYSA-N 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 150000003944 halohydrins Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 229940050176 methyl chloride Drugs 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- DFENKTCEEGOWLB-UHFFFAOYSA-N n,n-bis(methylamino)-2-methylidenepentanamide Chemical compound CCCC(=C)C(=O)N(NC)NC DFENKTCEEGOWLB-UHFFFAOYSA-N 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 239000001254 oxidized starch Substances 0.000 description 1
- 235000013808 oxidized starch Nutrition 0.000 description 1
- 108091008695 photoreceptors Proteins 0.000 description 1
- 230000029264 phototaxis Effects 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000001103 potassium chloride Substances 0.000 description 1
- 235000011164 potassium chloride Nutrition 0.000 description 1
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 1
- 229940088417 precipitated calcium carbonate Drugs 0.000 description 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 239000007870 radical polymerization initiator Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000002351 wastewater Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Paper (AREA)
Abstract
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明は、電子写真方式の複写機やプリンターなどに使
用される電子写真用転写紙に関する。DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to an electrophotographic transfer paper used in electrophotographic copying machines, printers, and the like.
(従来の技術)
従来、電子写真用転写紙としては、特開昭54−111
740号公報、特開昭54−22831号公報等に開示
されているように、填料としてタルク、カオリン,クレ
ー等が使用されてなる酸性紙が主流を占めている.しか
しながら、近年製紙業界においては、印刷や筆記用の上
質紙の製造に当たっては、填料として炭酸カルシウムを
用い、かつサイズ剤として中性サイズを使用することを
内容とする、いわゆる中性化の指向が高まっている。上
質紙を中性化することによる特長としては、安価な炭酸
カルシウムを填料として用いることにより用紙の製造コ
ストを低減しうること、更には用紙製造上の省エネルギ
ー,省資源、生産性向上、設備の延命、排水の浄化等の
諸目的を達成しうることである.このような中性抄紙技
術を電子写真用転写紙に応用した例としては、特開昭5
9−162560号公報、特開昭61−63854号公
報、特開昭61−67038号公報、特開昭62−69
94号公報等が挙げられるが,これらの場合の使用サイ
ジング剤としてはアルケニル無水コハク酸、アルキルケ
テンダイマーが開示されている.
(発明が解決しようとする問題点)
しかしながら、サイジング剤としてアルケニル無水コハ
ク酸またはアルキルケテンダイマーを用いた場合には、
電子写真用転写紙製造時に抄紙系のうち特にワイヤ一部
、プレス部、ドライヤ一部などに汚れが発生し、その結
果として成紙に斑点が生じる等の品質上の問題がある。(Prior art) Conventionally, as a transfer paper for electrophotography, Japanese Patent Application Laid-Open No. 54-111
As disclosed in Japanese Patent Publication No. 740 and Japanese Patent Application Laid-Open No. 54-22831, acidic papers containing talc, kaolin, clay, etc. as fillers are the mainstream. However, in recent years in the paper industry, there has been a trend toward so-called neutralization, which involves using calcium carbonate as a filler and a neutral size sizing agent in the production of high-quality paper for printing and writing. It's increasing. The advantage of neutralizing high-quality paper is that it can reduce paper manufacturing costs by using inexpensive calcium carbonate as a filler, and it can also save energy and resources in paper manufacturing, improve productivity, and save equipment. It is possible to achieve various purposes such as extending life and purifying wastewater. An example of applying such neutral papermaking technology to electrophotographic transfer paper is
9-162560, JP 61-63854, JP 61-67038, JP 62-69
No. 94, etc., discloses alkenyl succinic anhydride and alkyl ketene dimer as the sizing agent used in these cases. (Problems to be Solved by the Invention) However, when alkenyl succinic anhydride or alkyl ketene dimer is used as a sizing agent,
During the production of electrophotographic transfer paper, stains occur particularly in a part of the paper making system, such as a part of the wire, a press part, a part of the dryer, etc., and as a result, there are quality problems such as spots on the paper.
斯かる品質上の問題を解決するには,生じた汚れを洗浄
すればよいが、操業性が大幅に低下する不利がある。ま
た、アルキルケテンダイマーの特有の問題点としては、
成紙の摩擦係数が低いため、電子写真印刷時に転写紙が
重なって供給される等の成紙使用時の問題もある。In order to solve such quality problems, it is possible to wash away the dirt that has arisen, but this has the disadvantage of significantly reducing operability. In addition, problems specific to alkyl ketene dimers include:
Since the coefficient of friction of the formed paper is low, there are also problems when using the formed paper, such as transfer paper being fed in an overlapping manner during electrophotographic printing.
(問題点を解決するための千段)
本発明者らは、上記した従来技術の問題点を解決するた
め、鋭意研究を重ねたところ、内添サイズ剤として、特
定のスチレン系共重合体またはその4級化物を用いるこ
とにより、抄紙系の汚れが全く発生せず、かつ電子写真
用転写紙に最適の摩擦係数を有する紙が得られることを
見出し、本発明を完成するに至った.
即ち本発明は、パルプ繊維、サイズ剤および炭酸カルシ
ウム系填料を主成分としてなる電子写真用転写紙におい
て,該サイズ剤が、■スチレン類、ならびに
■一般式11)
(式中、R1は水素原子またはメチル基、R”およびR
3はそれぞれ同一または相異なって炭素数1〜4のアル
キル基、およびAは炭素数1〜3のアルキレン基を示す
)で表されるアミノアルキルエステル、その酸付加塩お
よびその4級塩から選ばれた少なくともl種、
および/または
〇一般式(2)
(式中、R’.R”およびR1はそれぞれ前記一龍式i
l+のそれらと同一であり、Bは炭素数1〜3のアルキ
レン基を示す)で表されるアミノアクリルアミド、その
酸付加塩およびその4級塩から選ばれた少なくとも1種
、
を横成モノマーとする水溶性又は水分散性共重合体であ
ることを特徴とする電子写真用転写紙に係る.
本発明で用いる填料である炭酸カルシウムとしては特に
制限はされず、重質炭酸カルシウム、沈降性炭酸カルシ
ウムなどの各種公知のものを使用できる.
本発明で用いるサイズ剤の構成単量体は、前記のように
スチレン類(以下、七ノマー■という)ならびにジアル
キルアミノアルキル(メタ)アクリレート(以下、モノ
マー■という)および/またはジアルキルアミノアルキ
ル(メタ)アクリルアミド(以下、モノマー■という)
である。(A Thousand Steps to Solving the Problems) In order to solve the problems of the prior art described above, the present inventors have conducted extensive research and found that a specific styrene copolymer or The present inventors have discovered that by using the quaternized product, it is possible to obtain paper that does not stain the papermaking system at all and has an optimal coefficient of friction for electrophotographic transfer paper, and has completed the present invention. That is, the present invention provides an electrophotographic transfer paper comprising pulp fiber, a sizing agent, and a calcium carbonate filler as main components, in which the sizing agent is 1) styrene, and 2) general formula 11) (wherein R1 is a hydrogen atom). or methyl group, R” and R
3 are the same or different and are each an alkyl group having 1 to 4 carbon atoms, and A is an alkylene group having 1 to 3 carbon atoms), acid addition salts thereof, and quaternary salts thereof; and/or 〇 General formula (2) (wherein R'.R'' and R1 are each the above-mentioned Ichiryu formula i
At least one selected from aminoacrylamide, an acid addition salt thereof, and a quaternary salt thereof, which are the same as those of l+, and B represents an alkylene group having 1 to 3 carbon atoms, are used as a lateral monomer. This invention relates to an electrophotographic transfer paper characterized by being a water-soluble or water-dispersible copolymer. The filler calcium carbonate used in the present invention is not particularly limited, and various known ones such as heavy calcium carbonate and precipitated calcium carbonate can be used. As mentioned above, the constituent monomers of the sizing agent used in the present invention include styrenes (hereinafter referred to as heptanomer Ⅰ), dialkylaminoalkyl (meth)acrylate (hereinafter referred to as monomer Ⅰ) and/or dialkylaminoalkyl (meth) ) Acrylamide (hereinafter referred to as monomer ■)
It is.
モノマー■とじては,スチレン、a−メチルスチレン、
ビニルトルエンが挙げられる。モノマー■とじては、N
.N−ジメチルアミノメチル(メタ)アクリレート、N
,N−ジメチルアミノエチル(メタ)アクリレート、N
,N−ジメチルアミノブロビル(メタ)アクリレート、
・N.N−ジエチルアミノメチル(メタ)アクリレート
、N,N−ジエチルアミノエチル(メタ)アクリレート
、N.N−ジエチルアミノブロビル(メタ)アクリレー
トなど、更にはこれらの酸付加塩、4級塩を例示できる
.酸付加塩としては、例えば塩酸、硫酸などの無機酸ま
たはギ酸、酢酸、プロビオン酸などの有機酸が付加した
水溶性の酸付加塩を例示できる.また、4級塩としては
、ハロゲン化アルキル、ハロゲン化ベンジル、エビハロ
ヒドリン等の公知の4級化剤により4級化してなる各種
をいう.またモノマー■としては、N,N−ジメチルア
ミノメチル(メタ)アクリルアミド、N,N−ジメチル
アミノエチル(メタ)アクリルアミド、N,N−ジメチ
ルアミノプロビル(メタ)アクリルアミド. N,N−
ジエチルアミノメチル(メタ)アクリルアミド、N,N
−ジエチルアミノエチル(メタ)アクリルアミド. N
.N−ジエチルアミノプロビル(メタ)アクリルアミド
など、更にはこれらの酸付加塩、4級塩を例示できる.
なお,酸付加塩,4級塩となす場合に使用される酸類お
よび4級化剤はいずれも前記と同様である。また、共重
合体の酸付加塩、4級塩となすには、あらかじめモノマ
ー段階で行えることは勿論のこと、共重合体を得た後に
変性しても良い。Monomers ■ include styrene, a-methylstyrene,
Examples include vinyltoluene. The monomer ■ is N
.. N-dimethylaminomethyl (meth)acrylate, N
, N-dimethylaminoethyl (meth)acrylate, N
, N-dimethylaminobrovir (meth)acrylate,
・N. N-diethylaminomethyl (meth)acrylate, N,N-diethylaminoethyl (meth)acrylate, N. Examples include N-diethylaminobrobyl (meth)acrylate, as well as acid addition salts and quaternary salts thereof. Examples of acid addition salts include water-soluble acid addition salts containing inorganic acids such as hydrochloric acid and sulfuric acid, or organic acids such as formic acid, acetic acid, and propionic acid. Furthermore, quaternary salts refer to various salts obtained by quaternizing with known quaternizing agents such as alkyl halides, benzyl halides, and shrimp halohydrin. The monomers (2) include N,N-dimethylaminomethyl (meth)acrylamide, N,N-dimethylaminoethyl (meth)acrylamide, and N,N-dimethylaminopropyl (meth)acrylamide. N, N-
Diethylaminomethyl (meth)acrylamide, N,N
-diethylaminoethyl (meth)acrylamide. N
.. Examples include N-diethylaminopropyl (meth)acrylamide, as well as acid addition salts and quaternary salts thereof.
Note that the acids and quaternizing agents used to form acid addition salts and quaternary salts are the same as those described above. Further, to form an acid addition salt or a quaternary salt of the copolymer, it can be done in advance at the monomer stage, or it may be modified after the copolymer is obtained.
前記各種構成モノマーの使用割合は、得られる共重合体
中に、モノマー■は40〜95モルi程度、好ましくは
60〜90モル2である。40モル2未満の場合にはサ
イズ効果が不充分となり、また95モルiを越える場合
にはサイズ剤のバルブへの定着が不充分となり,いずれ
も好ましくない。モノマー■、モノマー■はいずれも5
〜60モルX程度、好ましくはlO〜40モル1である
。5モルi未満の場合にはサイズ剤のパルプへの定着が
不充分となり、また60モル1を越える場合にはサイズ
効果が不充分となり、いずれも好ましくない。また、モ
ノマー■とモノマー◎の両者を併用した場合にはそれら
の合計量が得られる共重合体に対して5〜60モル1程
度、好ましくは10〜40モルiとされる.なお、共重
合体は本発明の目的を逸脱せず、しかもその効果を保持
しつる限度において、上記モノマーの一部に代えてその
他の七ノマーを使用することができる.当該他の七ノマ
ーとしては、例えば酢酸ビニル、アクリル酸の低級アル
コールエステル、メタクリル酸の低級アルコールエステ
ル、アクリロニトリルなどを挙げることができ、該モノ
マーの使用量は共重合体中20モル1程度以下とされる
。The proportion of the various constituent monomers used is about 40 to 95 moles, preferably 60 to 90 moles, of monomer (1) in the resulting copolymer. If it is less than 40 moles, the sizing effect will be insufficient, and if it exceeds 95 moles, the fixing of the sizing agent to the bulb will be insufficient, both of which are not preferred. Monomer ■ and monomer ■ are both 5
~60 mol X or so, preferably lO~40 mol 1. If the amount is less than 5 moles, the fixation of the sizing agent to the pulp will be insufficient, and if it exceeds 60 moles, the sizing effect will be insufficient, both of which are not preferred. In addition, when both monomer (■) and monomer (◎) are used together, the total amount thereof is about 5 to 60 mol 1, preferably 10 to 40 mol i, based on the resulting copolymer. In addition, in the copolymer, other heptanomers may be used in place of some of the above monomers, as long as they do not deviate from the purpose of the present invention and still maintain their effects. Examples of the other heptanomer include vinyl acetate, lower alcohol ester of acrylic acid, lower alcohol ester of methacrylic acid, acrylonitrile, etc., and the amount of the monomer used is about 20 mol 1 or less in the copolymer. be done.
前記共重合体の製造方法としては、特に制限はされず、
各種公知の方法を採用できる。例えば,過酸化水素,過
硫酸カリウムなどの水溶性ラジカル重合開始剤を用いて
、前記単量体混合物を水性媒体中で単量体濃度5〜50
重量1、温度50〜95℃で、 1〜10時間程度反応
させればよい.前記で得られたサイズ剤を使用して本発
明の電子写真用転写紙を製造するに当たっては、コピー
適性、走光性、カール性等の電子写真複写機適性を付与
するために、以下に示す原料の配゛合、調整、製造条件
のコントロールが行われる(特公昭44−3673号公
報、特公昭46−24199号公報、特公昭55−47
385号公報).
具体的には、サイズ剤はパルブに対して通常0.01−
1.0重量一程度、また填料はパルブに対して通常2〜
20重量1程度となるよう内部添加され、抄造される.
また、適当なコピー画像濃度を維持し、バックグランド
(白地部分)の汚れを防ぐために、塩化ナトリウム、塩
化カリウム、スチレンーマレイン酸共重合体、第4級ア
ンモニウム塩などの導電剤を抄紙機のサイズプレスで表
面塗布することにより転写紙の表面電気抵抗(JISC
−2111による)を10”〜 l010Ω(相対18
度651、温度20℃)にする。また、転写紙の部分的
吸収による膨潤やカールが発生すると、転写時に複写紙
の感光体と転写紙との密接度が低下し、コピー画像濃度
の低下やコピーの部分的な抜けが発生するのでこれを防
止するために紙の水分を4.5〜5.51にして保管時
に吸脱湿が発生しないよう、防湿包装紙で包装する。The method for producing the copolymer is not particularly limited,
Various known methods can be employed. For example, using a water-soluble radical polymerization initiator such as hydrogen peroxide or potassium persulfate, the monomer mixture is prepared in an aqueous medium at a monomer concentration of 5 to 50%.
The reaction may be carried out at a weight of 1 and a temperature of 50 to 95°C for about 1 to 10 hours. When producing the electrophotographic transfer paper of the present invention using the sizing agent obtained above, the following raw materials are used to impart suitability for electrophotographic copying machines such as copyability, phototaxis, and curling properties. The composition, adjustment, and manufacturing conditions are controlled (Japanese Patent Publication No. 44-3673, Japanese Patent Publication No. 24199-1972, Japanese Patent Publication No. 55-47)
Publication No. 385). Specifically, the size of the sizing agent is usually 0.01-
1.0 weight, and the filler is usually 2 to 1 weight per pulp.
It is added internally so that the weight is about 1:20, and the paper is made into paper.
In addition, in order to maintain appropriate copy image density and prevent background (white background) stains, conductive agents such as sodium chloride, potassium chloride, styrene-maleic acid copolymer, and quaternary ammonium salts are added to the paper machine. The surface electrical resistance of the transfer paper (JISC
-2111) from 10” to l010Ω (relative 18
651°C, temperature 20°C). In addition, if swelling or curling occurs due to partial absorption of the transfer paper, the closeness between the photoreceptor of the copy paper and the transfer paper decreases during transfer, resulting in a decrease in copy image density and partial omission of copies. To prevent this, the moisture content of the paper is set to 4.5 to 5.51, and the paper is wrapped in moisture-proof wrapping paper to prevent moisture absorption and desorption during storage.
(実廁例)
以下、参考例,実施例および比較例を挙げて本発明を具
体的に説明するが、本発明はこれら実施例に限定される
ものではない。尚、各例中、部及び%は特記しない限り
すべて重量基準である.参考例l
攪拌装置、温度計、冷却管および滴下ロートを備えた反
応装置にイソプロビルアルコール1000部を仕込み、
還流温度まで加温し、ついで滴下ロートより、スチレン
780部、N,N−ジメチルアミンエチルメタクリレー
ト240部、アゾイソブチロニトリル20部からなる混
合溶液を2時間かけて反応系内に滴下し、更に同温度で
5時間保持し、反応を完結させた.ついで、得られた反
応溶液からイソブロビルアルコール約750部を留去し
、更に酢酸92部および水4200部を添加して溶解さ
せることにより、サイズ剤Aを得た.
参考例2
参考例lで得たサイズ剤に,更にエビクロルヒドリン1
42部を加え、80〜85℃で3時間反応を行い、サイ
ズ剤Bを得た.
参考例3
参考例lにおいて、N.N−ジメチルアミノエチルメタ
クリレートに代えてN,N−ジメチルアミノブロビルア
クリルアミドを使用したほかは同様にして反応を行い、
サイズ剤Cを得た。(Practical Examples) Hereinafter, the present invention will be specifically described with reference to reference examples, working examples, and comparative examples, but the present invention is not limited to these examples. In each example, all parts and percentages are based on weight unless otherwise specified. Reference Example 1 1000 parts of isopropyl alcohol was charged into a reaction apparatus equipped with a stirrer, a thermometer, a cooling tube, and a dropping funnel.
After heating to reflux temperature, a mixed solution consisting of 780 parts of styrene, 240 parts of N,N-dimethylamine ethyl methacrylate, and 20 parts of azoisobutyronitrile was dropped into the reaction system over 2 hours from a dropping funnel. The reaction was further maintained at the same temperature for 5 hours to complete the reaction. Then, about 750 parts of isobrobyl alcohol was distilled off from the resulting reaction solution, and 92 parts of acetic acid and 4,200 parts of water were added and dissolved to obtain Sizing Agent A. Reference Example 2 In addition to the sizing agent obtained in Reference Example 1, shrimp chlorohydrin 1
Sizing agent B was obtained by adding 42 parts and carrying out a reaction at 80 to 85°C for 3 hours. Reference Example 3 In Reference Example 1, N. The reaction was carried out in the same manner except that N,N-dimethylaminobrobylacrylamide was used instead of N-dimethylaminoethyl methacrylate,
Sizing agent C was obtained.
参考例4
参考例2において、N,N−ジメチルアミノエチルメタ
クリレートに代えてN,N−ジメチルアミノプロビルア
クリルアミドを使用したほかは同様にして反応を行い、
サイズ剤Dを得た.
参考例5
参考例lにおいて、N,N−ジメチルアミノエチルメタ
クリレートに代えてN,N−ジメチルアミノブロビルア
クリルアミドをメチルクロライドにより4級化したモノ
マーを使用したほかは同様にして反応を行い,サイズ剤
Eを得た.
実施例1〜5および比較例1〜2
L−BKP (フリーネス400a+l csf )
とN−BKP (フリーネス50(lml csf
)の配合比が80+20のバルブを用い、第1表に示し
た薬品処方により、長網式抄紙機( 500m/分)に
て抄造し、次に表面サイズ剤として酸化デンブンIg/
rdおよび塩化ナトリウム0.1g/tn”を塗布し
て用紙を作成した.この用紙を抄造する際のプレスロー
ルの汚れをドクター付着量として測定した.電子写真用
転写紙の物性として,平滑度(J.TAPPI No.
5の王研式による)と静摩擦係数( J.TAPPI
No. 30の水平法による)を測定した.また、重送
(用紙が数枚重なって送られること)に関係がある,上
下2枚間の静摩擦係数の差の最大値(差が少なく、摩擦
係数が一定なほど重送しにくい)を求めた.さらに、重
送回数の測定は、電子写真複写機(キヤノンNP−48
35、キヤノン■製)を用いて行い. 1000枚複写
したときに発生した重送回数で表した.E以下余白]
(発明の効果)
本発明の電子写真用転写紙抄造工程中で抄造機械に汚れ
が発生しないため、成紙の商品価値が向上するとともに
、洗浄作業などが不要となるため抄紙作業能率も大幅に
改善できる。更には得られる転写紙のN擦係数が適性範
囲にあるため、複写作業時に転写紙の重ね送りの問題が
解消されるなどの多大の効果が奏せられる。Reference Example 4 The reaction was carried out in the same manner as in Reference Example 2, except that N,N-dimethylaminopropylacrylamide was used instead of N,N-dimethylaminoethyl methacrylate.
Sizing agent D was obtained. Reference Example 5 The reaction was carried out in the same manner as in Reference Example 1 except that a monomer obtained by quaternizing N,N-dimethylaminobrobylacrylamide with methyl chloride was used instead of N,N-dimethylaminoethyl methacrylate. Agent E was obtained. Examples 1 to 5 and Comparative Examples 1 to 2 L-BKP (Freeness 400a+l csf)
and N-BKP (freeness 50 (lml csf
) using a valve with a blending ratio of 80 + 20, paper was made using a fourdrinier paper machine (500 m/min) according to the chemical formulation shown in Table 1, and then oxidized starch Ig/
rd and sodium chloride at 0.1 g/tn". The dirt on the press roll during paper making of this paper was measured as the amount of doctor adhesion. The physical properties of electrophotographic transfer paper include smoothness ( J.TAPPI No.
5) and static friction coefficient (J. TAPPI
No. 30 horizontal method) was measured. In addition, the maximum value of the difference in the coefficient of static friction between the upper and lower two sheets, which is related to double feeding (feeding several sheets overlapping each other), was calculated (the smaller the difference and the more constant the friction coefficient, the harder it is to cause double feeding). Ta. Furthermore, the number of double feeds was measured using an electrophotographic copying machine (Canon NP-48).
35, manufactured by Canon ■). Expressed as the number of double feeds that occurred when 1000 copies were made. Margin below E] (Effects of the invention) Since no stains are generated on the paper-making machine during the electrophotographic transfer paper-making process of the present invention, the commercial value of the paper is improved, and the paper-making process is improved because cleaning work etc. is no longer necessary. Efficiency can also be greatly improved. Furthermore, since the N friction coefficient of the obtained transfer paper is within the appropriate range, great effects such as solving the problem of overlapping transfer paper feeding during copying work can be achieved.
荒川化学工業株式会社Arakawa Chemical Industry Co., Ltd.
Claims (1)
成分としてなる電子写真用転写紙において、該サイズ剤
が、 (a)スチレン類、ならびに (b)一般式(1) ▲数式、化学式、表等があります▼ (式中、R^1は水素原子またはメチル基、R^2およ
びR^3はそれぞれ同一または相異なって炭素数1〜4
のアルキル基、およびAは炭素数1〜3のアルキレン基
を示す)で表されるアミノアルキルエステル、その酸付
加塩およびその4級塩から選ばれた少なくとも1種、 および/または (c)一般式(2) ▲数式、化学式、表等があります▼ (式中、R^1、R^2およびR^3はそれぞれ前記一
般式(1)のそれらと同一であり、Bは炭素数1〜3の
アルキレン基を示す)で表されるアミノアクリルアミド
、その酸付加塩およびその4級塩から選ばれた少なくと
も1種、 を構成モノマーとする水溶性又は水分散性共重合体であ
ることを特徴とする電子写真用転写紙。[Claims] An electrophotographic transfer paper containing pulp fiber, a sizing agent, and a calcium carbonate filler as main components, wherein the sizing agent comprises (a) styrenes, and (b) general formula (1) ▲Math. , chemical formulas, tables etc.
and/or (c) general Formula (2) ▲There are mathematical formulas, chemical formulas, tables, etc.▼ (In the formula, R^1, R^2, and R^3 are each the same as those in the general formula (1) above, and B has 1 to It is characterized by being a water-soluble or water-dispersible copolymer comprising as a constituent monomer at least one member selected from aminoacrylamide represented by (3) representing an alkylene group, an acid addition salt thereof, and a quaternary salt thereof. Transfer paper for electrophotography.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1308228A JP2558532B2 (en) | 1989-11-27 | 1989-11-27 | Electrophotographic transfer paper |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1308228A JP2558532B2 (en) | 1989-11-27 | 1989-11-27 | Electrophotographic transfer paper |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH03167397A true JPH03167397A (en) | 1991-07-19 |
JP2558532B2 JP2558532B2 (en) | 1996-11-27 |
Family
ID=17978471
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1308228A Expired - Lifetime JP2558532B2 (en) | 1989-11-27 | 1989-11-27 | Electrophotographic transfer paper |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2558532B2 (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5562974A (en) * | 1992-07-08 | 1996-10-08 | Nippon Paper Industries Co., Ltd. | Permanent paper |
JP2000199196A (en) * | 1998-12-25 | 2000-07-18 | Japan Pmc Corp | Paper for ppc excellent in ink jet suitability and its production |
JP2005248338A (en) * | 2004-03-02 | 2005-09-15 | Harima Chem Inc | Cationic surface sizing agent and paper using the same |
WO2009013913A1 (en) * | 2007-07-26 | 2009-01-29 | Harima Chemicals, Inc. | Internal sizing agent for papermaking and use thereof |
US7988826B2 (en) | 2006-03-30 | 2011-08-02 | Harima Chemicals, Inc. | Cationic surface sizing agent and paper coated with the same |
-
1989
- 1989-11-27 JP JP1308228A patent/JP2558532B2/en not_active Expired - Lifetime
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5562974A (en) * | 1992-07-08 | 1996-10-08 | Nippon Paper Industries Co., Ltd. | Permanent paper |
JP2000199196A (en) * | 1998-12-25 | 2000-07-18 | Japan Pmc Corp | Paper for ppc excellent in ink jet suitability and its production |
JP2005248338A (en) * | 2004-03-02 | 2005-09-15 | Harima Chem Inc | Cationic surface sizing agent and paper using the same |
US7988826B2 (en) | 2006-03-30 | 2011-08-02 | Harima Chemicals, Inc. | Cationic surface sizing agent and paper coated with the same |
WO2009013913A1 (en) * | 2007-07-26 | 2009-01-29 | Harima Chemicals, Inc. | Internal sizing agent for papermaking and use thereof |
US8241462B2 (en) | 2007-07-26 | 2012-08-14 | Harima Chemicals, Inc. | Papermaking internal sizing agent and use thereof |
JP5043112B2 (en) * | 2007-07-26 | 2012-10-10 | ハリマ化成株式会社 | Internal sizing agent for papermaking and its use |
Also Published As
Publication number | Publication date |
---|---|
JP2558532B2 (en) | 1996-11-27 |
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