JPS58113944A - Production of electrostatic latent image developer - Google Patents
Production of electrostatic latent image developerInfo
- Publication number
- JPS58113944A JPS58113944A JP56213599A JP21359981A JPS58113944A JP S58113944 A JPS58113944 A JP S58113944A JP 56213599 A JP56213599 A JP 56213599A JP 21359981 A JP21359981 A JP 21359981A JP S58113944 A JPS58113944 A JP S58113944A
- Authority
- JP
- Japan
- Prior art keywords
- latent image
- toner
- carboxylic groups
- styrene
- electrostatic latent
- 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.)
- Pending
Links
- 238000004519 manufacturing process Methods 0.000 title claims description 4
- 239000002253 acid Substances 0.000 claims abstract description 14
- 238000000034 method Methods 0.000 claims abstract description 14
- 238000011161 development Methods 0.000 claims abstract description 13
- 229920003002 synthetic resin Polymers 0.000 claims abstract description 13
- 239000000057 synthetic resin Substances 0.000 claims abstract description 13
- 230000009191 jumping Effects 0.000 claims abstract description 7
- 238000002156 mixing Methods 0.000 claims abstract description 7
- 239000000975 dye Substances 0.000 claims abstract description 6
- 239000000049 pigment Substances 0.000 claims abstract 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 8
- 239000002245 particle Substances 0.000 abstract description 16
- 230000005684 electric field Effects 0.000 abstract description 10
- 239000000203 mixture Substances 0.000 abstract description 7
- 229920006026 co-polymeric resin Polymers 0.000 abstract description 5
- 230000010287 polarization Effects 0.000 abstract description 3
- PYSRRFNXTXNWCD-UHFFFAOYSA-N 3-(2-phenylethenyl)furan-2,5-dione Chemical compound O=C1OC(=O)C(C=CC=2C=CC=CC=2)=C1 PYSRRFNXTXNWCD-UHFFFAOYSA-N 0.000 abstract 1
- 229920000147 Styrene maleic anhydride Polymers 0.000 abstract 1
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 20
- 229920005989 resin Polymers 0.000 description 12
- 239000011347 resin Substances 0.000 description 12
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 10
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 5
- 229910052782 aluminium Inorganic materials 0.000 description 5
- 229910052742 iron Inorganic materials 0.000 description 5
- 230000000694 effects Effects 0.000 description 4
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 229910002012 Aerosil® Inorganic materials 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 229920006243 acrylic copolymer Polymers 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 238000011981 development test Methods 0.000 description 2
- 239000010419 fine particle Substances 0.000 description 2
- 229920006122 polyamide resin Polymers 0.000 description 2
- 239000004645 polyester resin Substances 0.000 description 2
- 229920001225 polyester resin Polymers 0.000 description 2
- 238000010298 pulverizing process Methods 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- KWORKYDIARWARF-UHFFFAOYSA-N N-(4-chloro-2-methylphenyl)-4-[(4-chloro-2-methylphenyl)diazenyl]-3-hydroxynaphthalene-2-carboxamide Chemical compound Cc1cc(Cl)ccc1NC(=O)c1cc2ccccc2c(N=Nc2ccc(Cl)cc2C)c1O KWORKYDIARWARF-UHFFFAOYSA-N 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 241001255907 Tonica Species 0.000 description 1
- 125000005396 acrylic acid ester group Chemical group 0.000 description 1
- 238000005054 agglomeration Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 125000003368 amide group Chemical group 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000010292 electrical insulation Methods 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- WOLATMHLPFJRGC-UHFFFAOYSA-N furan-2,5-dione;styrene Chemical compound O=C1OC(=O)C=C1.C=CC1=CC=CC=C1 WOLATMHLPFJRGC-UHFFFAOYSA-N 0.000 description 1
- 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 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- RAPZEAPATHNIPO-UHFFFAOYSA-N risperidone Chemical compound FC1=CC=C2C(C3CCN(CC3)CCC=3C(=O)N4CCCCC4=NC=3C)=NOC2=C1 RAPZEAPATHNIPO-UHFFFAOYSA-N 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 229920001909 styrene-acrylic polymer Polymers 0.000 description 1
- 125000001174 sulfone group Chemical group 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 238000007794 visualization technique Methods 0.000 description 1
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G9/00—Developers
- G03G9/08—Developers with toner particles
- G03G9/087—Binders for toner particles
- G03G9/08784—Macromolecular material not specially provided for in a single one of groups G03G9/08702 - G03G9/08775
- G03G9/08791—Macromolecular material not specially provided for in a single one of groups G03G9/08702 - G03G9/08775 characterised by the presence of specified groups or side chains
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G9/00—Developers
- G03G9/08—Developers with toner particles
- G03G9/0802—Preparation methods
- G03G9/081—Preparation methods by mixing the toner components in a liquefied state; melt kneading; reactive mixing
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G9/00—Developers
- G03G9/08—Developers with toner particles
- G03G9/0802—Preparation methods
- G03G9/0815—Post-treatment
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G9/00—Developers
- G03G9/08—Developers with toner particles
- G03G9/087—Binders for toner particles
- G03G9/08784—Macromolecular material not specially provided for in a single one of groups G03G9/08702 - G03G9/08775
- G03G9/08795—Macromolecular material not specially provided for in a single one of groups G03G9/08702 - G03G9/08775 characterised by their chemical properties, e.g. acidity, molecular weight, sensitivity to reactants
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Developing Agents For Electrophotography (AREA)
Abstract
Description
【発明の詳細な説明】
本発明は非接触型の潜像可視化方法に用いる現像剤の製
造法に関するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing a developer used in a non-contact latent image visualization method.
静電潜像を現象する方式は、乾式現像方法が主流となり
、その中でも磁気ブラシ法が広く使用されている。この
方法は接触型現像法であるために、カラー現像を行う際
に先に現像された可視像に1次に現像される色調の異な
るトナーが重なり易く1色まじりが起るため1色調の不
鮮明が生じる不都合な問題を抱えている。゛乾式現像法
の他の方式としてジャンプ法と呼ばれる方法があるが、
現状では磁性−成分トナーをf11用しているために、
率性粉体である酸化鉄をトナーに混合する必要かあQ%
黒色以外の色調のトナーを作ることが不可能であった。Dry developing methods are the mainstream method for developing electrostatic latent images, and among these, the magnetic brush method is widely used. Since this method is a contact development method, when color development is performed, toners of different tones developed first tend to overlap with the visible image developed first, resulting in mixing of one color. It has the inconvenient problem of blurring.゛Another method of dry development is called the jump method.
Currently, since magnetic component toner is used for F11,
Q% Is it necessary to mix iron oxide, which is a powder, into the toner?
It has been impossible to create toners with tones other than black.
本発明では米国特許第3203394号、第32321
90号などに開示されているジャンプ法と呼ばれる非磁
性、非接触型現像法に適したトナーを作製することによ
り、カラー現像を可能にすることを具現化したものであ
る。この現像法は潜像保持体と一定の距離を隔てた現像
部材が設けられ、トナー粒子は現像部材表面に例えばブ
レーク゛を使つて薄層状に撒き拡げられる。現像部材と
潜像保持体の間には交番電界が印加され、トナー粒子は
交番電界の働きによって現像部材と潜像保持体0間をジ
ャンプしながら往復運動を行なう。In the present invention, US Pat.
The present invention embodies the idea of making color development possible by producing a toner suitable for a non-magnetic, non-contact development method called the jump method, which is disclosed in No. 90 and others. In this developing method, a developing member is provided at a certain distance from the latent image carrier, and toner particles are spread in a thin layer on the surface of the developing member using, for example, a breaker. An alternating electric field is applied between the developing member and the latent image holder, and the toner particles perform reciprocating motion while jumping between the developing member and the latent image holder 0 due to the action of the alternating electric field.
その際に画像潜像に向ったトナー粒子は潜像の静電引力
により付着し、非画像部ではトナー粒子は除かれた状態
となって、現像を終了させる方法である。At this time, the toner particles directed toward the latent image adhere to the latent image due to the electrostatic attraction of the latent image, and the toner particles are removed from the non-image area, thereby completing development.
この現像法に用いられるトナーは、現像部材表面と摩擦
帯電またはコロナ放電により、正または負のどちらか一
方に均一に帯電しなければならないが、さらに重要な条
件として現像部材と潜像保持体との間に印加された交番
電界によってンヤンプする性質を有することである。転
写可能であるためには電気絶縁性を有し、多くの色調に
着色可能であり、かつジャンプ能を有次のような結論を
得た。公知のトナー用樹脂成分としては、一般に帯電極
性をコントロールし易いことから、エポキシ樹脂、スチ
レン樹脂。The toner used in this development method must be uniformly charged either positively or negatively by frictional charging or corona discharge with the surface of the developing member, but an even more important condition is that the developing member and latent image carrier It has the property of changing depending on the alternating electric field applied during the period. We concluded that in order to be transferable, it must have electrical insulation properties, be colored in many tones, and have jump ability. Known resin components for toners include epoxy resins and styrene resins because they are generally easy to control charging polarity.
ポリエステル樹脂などが用いられている。通常はこれら
の樹脂類に帯電極性フントロールのために染料または特
定の添加剤を混入させることが行なわれている。一方接
性基を導入した合成樹脂は、その極性基の種類によって
帯電極性が異なることも、例えば特公昭44−1707
4にすでに知られていることである。しかし、これら極
性基の導入だけではトナーの摩擦帯電量は十分でなく、
染料または特定の添加剤の混合がなくては実用性のある
トナーが得られないのが実状である。本発明者等はトナ
ー成分樹脂中の棒慴基とジャンピング現象の関係を調べ
た結果、カルボキシル基を有する合成樹脂がジャンピン
グ現象を起し易く、他の極性基例えば水酸基、アミ7基
、スルホン基などに較べてジャンプ効果が顕著であった
0合成樹脂分子の末端または側鎖に結合している。カル
ボキシル基は電界中に置かれることにより分極を促進す
るため、一時的1どトナー粒子は誘電率の大なる状態に
なり、電気力線の方向に応じて飛躍するものと考えられ
る0合成樹脂の種類としては、カルボキシル基を導入す
るに容易なものが使用できる6例えばスチレ/・アクリ
ル酸エステル共重合m脂。Polyester resin etc. are used. Usually, these resins are mixed with dyes or specific additives for charging polar funtrols. Synthetic resins into which a unilaterally tangential group has been introduced may have different charging polarity depending on the type of polar group.
4 is already known. However, simply introducing these polar groups is not sufficient to increase the triboelectric charge of the toner.
The reality is that a toner of practical use cannot be obtained without the addition of dyes or specific additives. As a result of investigating the relationship between the carboxyl groups in toner component resins and the jumping phenomenon, the present inventors found that synthetic resins having carboxyl groups are more likely to cause the jumping phenomenon, and other polar groups such as hydroxyl groups, amide groups, sulfone groups, etc. The jump effect was more pronounced than that of 0. It is bonded to the end or side chain of the synthetic resin molecule. Since carboxyl groups promote polarization when placed in an electric field, the toner particles temporarily become in a state with a high dielectric constant, which is thought to increase depending on the direction of the electric field lines. As for types, those that can easily introduce carboxyl groups can be used, such as styrene/acrylic acid ester copolymer resin.
スチレン・マレイン酸共重合樹脂、ポリエステル樹脂、
その他が挙げられる。導入されたカルボキシル基は、摩
擦帯電制御に十分でなく、染料または添加剤の混合によ
り、正または負を示すようにコントロールせねばならな
い。次にトナーの組成を具体化するために製造法を例示
する。Styrene/maleic acid copolymer resin, polyester resin,
Other examples include: The introduced carboxyl group is not sufficient to control triboelectrification, and must be controlled to exhibit positive or negative properties by mixing dyes or additives. Next, a manufacturing method will be illustrated to specify the composition of the toner.
実施例1
スチレン80gとアクリル酸メチル19g、アクリル酸
1.5gを共重合し、軟化点130℃、酸価12の塊状
樹脂を得た。Example 1 80 g of styrene, 19 g of methyl acrylate, and 1.5 g of acrylic acid were copolymerized to obtain a bulk resin having a softening point of 130° C. and an acid value of 12.
スチレン・アクリル共重合樹脂 100gポリアミ
ド樹脂(ポリマイドS−40E三洋化成) 20g
オイルブルーnN(オリエント化学)
10g上記配合を溶融混合した後、冷却粉砕を行なった
。粉砕トナーは10μ〜20μの粒径を有し。Styrene/acrylic copolymer resin 100g Polyamide resin (Polymide S-40E Sanyo Chemical) 20g
Oil Blue nN (Orient Chemical)
After melt-mixing 10 g of the above blend, cooling and pulverization were performed. The crushed toner has a particle size of 10μ to 20μ.
アルミニウムまたは鉄との摩擦帯電では正極性を示すこ
とが確認された。現像試験の結果、現像部材と感光ドラ
ムとの間隔を容易にジャンプし、充分な現像が行なわれ
ることが確認された。It was confirmed that triboelectrification with aluminum or iron shows positive polarity. As a result of the development test, it was confirmed that the distance between the developing member and the photosensitive drum could be easily jumped and sufficient development could be performed.
実施例2
スチレン97g、無水マレイン酸3gを共重合して軟化
点140℃酸(I aoの塊状樹脂を得た。Example 2 97 g of styrene and 3 g of maleic anhydride were copolymerized to obtain a bulk resin with a softening point of 140° C. acid (I ao).
スチレン・無水マレイン酸共重合樹脂 100
gポリアミド樹脂(ポリマイドS−40E三洋化成)
30gオイルレッドROB−B(オリエント化学)
10g0g上記配溶融混合し、冷却粉砕してlOμ
〜加μ粒径のトナーを得た。アルミニウムまたは鉄との
摩擦帯電極性は正を示し、現像部材と感光ドラムの間隔
を実施例1と同一条件でトナー粒子は十分にジャンプ現
像することが確認された。Styrene/maleic anhydride copolymer resin 100
g Polyamide resin (Polymide S-40E Sanyo Chemical)
30g Oil Red ROB-B (Orient Chemical)
10g0g of the above melted mixture, cooled and pulverized to lOμ
A toner having a particle size of .mu.m to .mu.m was obtained. The polarity of frictional charging with aluminum or iron was positive, and it was confirmed that the toner particles were sufficiently jump-developed under the same conditions as in Example 1 for the distance between the developing member and the photosensitive drum.
実施例3
スチレン80gとアクリル酸メチル20 gを共重合し
て軟化点120℃の塊状樹脂を得た。Example 3 80 g of styrene and 20 g of methyl acrylate were copolymerized to obtain a bulk resin having a softening point of 120°C.
実施例1で示された配合で溶融混合した後、冷却粉砕を
行い、10μ〜20μ粒径のトナーを得た。After melt-mixing according to the formulation shown in Example 1, cooling and pulverization were performed to obtain a toner having a particle size of 10 μm to 20 μm.
アル4ニウムまたは鉄との摩擦帯電極性は正を示したが
、現像部材と感光ドラム間の交番電界が実施例1と同一
ではトナー粒子がジャンプせず5交番電界を2倍に増加
してはじめてジャンプ現像が開始された。The polarity of frictional charging with aluminum or iron was positive, but when the alternating electric field between the developing member and the photosensitive drum was the same as in Example 1, the toner particles did not jump, but only when the alternating electric field was doubled. Jump development has started.
実施例4
スチ1ルン80g、アクリル酸メチル7Flyアクリル
酸3gを共重合させ、軟化点145℃、酸価23の塊状
樹脂を得た。Example 4 80 g of styrene and 3 g of methyl acrylate and 7Fly acrylic acid were copolymerized to obtain a bulk resin having a softening point of 145° C. and an acid value of 23.
スチレン・アクリル共重合樹脂 10
0gオイルスカーレノト (オリエント化学)5gパー
マネントカーミンBST(大口m化) 10g
上記の配合を溶融混合し、冷却粉砕して1071〜20
μ粒径のトナーを得た。このトナーに対して0.5wt
%の微粒子ンリカ会アエロンルR−972(日本7エロ
ジル)をトナーに加え充分に攪nti合した。アルミニ
ウムまたは鉄との摩擦帯電極性は負・を示した。現像試
験の結果、現像部材と感光ドラム間をトナー粒子がジャ
ンプするに要するり番電界は実施例1で印加された電界
よりも低電界で十分であった。Styrene/acrylic copolymer resin 10
0g Oil Scarlenoto (Orient Chemical) 5g Permanent Carmine BST (Large m) 10g
The above formulation was melt mixed, cooled and crushed to give 1071-20
A toner with μ particle size was obtained. 0.5wt for this toner
% of fine particles of Nrikakai Aeronlu R-972 (Japan 7 Erosil) were added to the toner and thoroughly mixed. The frictional charge polarity with aluminum or iron was negative. As a result of the development test, an electric field lower than the electric field applied in Example 1 was sufficient for toner particles to jump between the developing member and the photosensitive drum.
実施例5
スチレン80g、7グリル酸メチル7g+アクリル酸3
gを共重合させ、軟化点145℃、酸価23の塊状樹脂
を得た。Example 5 80g of styrene, 7g of methyl 7glylate + 3g of acrylic acid
g was copolymerized to obtain a bulk resin having a softening point of 145° C. and an acid value of 23.
スチレンアクリル共重合m脂100 gカーボンブラン
ク 5gスピロンプラノクBH(保
土谷化学)5g上記配合を溶融混合し、冷却粉砕してl
Oμ〜加μ粒径のトナーを得た。アルミニウムまたは鉄
との摩擦帯電極性は負を示した。さらに実施例4に見ら
れる如く、微粒子ンリカ(アエロジルR−972日本ア
エロジル)をトナーに対して0.5wt%加え、充分に
攪拌混合することにすってトナーの流動性が増加し、現
像部材上への撒布が容易となり、かつ均一になった。、
またジャ/ピング現像の効果は実施例4と同等にすぐれ
たものであった。Styrene acrylic copolymer resin 100 g Carbon blank 5 g Spiron Planok BH (Hodogaya Chemical) 5 g The above formulation was melted and mixed, cooled and crushed.
A toner having a particle size of Oμ to +μ was obtained. The frictional charge polarity with aluminum or iron was negative. Furthermore, as seen in Example 4, by adding 0.5 wt% of fine particle tonica (Aerosil R-972 Nippon Aerosil) to the toner and thoroughly stirring and mixing, the fluidity of the toner was increased and the surface of the developing member was increased. The spraying becomes easier and more uniform. ,
Furthermore, the effect of japping/ping development was as excellent as in Example 4.
本発明に使用される合成樹脂中のカルボキンル基含有量
は酸価5〜30の範囲が適正である。The appropriate carboquine group content in the synthetic resin used in the present invention is within the range of acid value 5 to 30.
カルボキシル基はトナー粒子の誘電分極を大きくさせる
効果を有しているので、カルボキシル基を多く含有する
合成樹脂をトナー成分として使用する方がトナーのジャ
ンビ/グ効果は大きくなると考えられる。しかし酸価が
大きくなると樹脂の軟化点が上昇し、トナーの適正定r
、温度の調整が困難になる。トナーの定着温度は一般に
120℃〜150℃の範囲のものが用いられているので
、この温度範囲が得られる合成樹脂の軟化点と酸価の関
係を求めた結果、酸価が高い合成樹脂はど軟化点が高く
なる傾向があった。また酸価が加重上の合成樹脂を用い
たトナーでは、トナー粒子間の凝集によると思われる龜
現象からトナーめ流動性が低下する傾向があり、流動性
の悪いトナーでは現像部材表面に撒歪する際にトナ一層
の厚さに均一性を欠き、その結果画像の均一性を損う。Since carboxyl groups have the effect of increasing the dielectric polarization of toner particles, it is thought that the use of a synthetic resin containing a large amount of carboxyl groups as a toner component increases the Jambi/G effect of the toner. However, as the acid value increases, the softening point of the resin increases, and the proper r
, temperature adjustment becomes difficult. Since the fixing temperature of toner is generally in the range of 120°C to 150°C, we determined the relationship between the softening point and acid value of synthetic resins that can achieve this temperature range, and found that synthetic resins with high acid values are There was a tendency for the softening point to become higher. In addition, toners using synthetic resins with high acid values tend to have poor fluidity due to a cloud phenomenon that is thought to be caused by agglomeration between toner particles, and toners with poor fluidity tend to cause distortion on the surface of the developing member. When printing, the thickness of the toner layer lacks uniformity, resulting in a loss of uniformity of the image.
これらの諸性質を満足させる必要からトナーに用いられ
る合成樹脂の酸価は自から実用可能な範囲が決定される
べきである。適正酸価を求めるには実際に現像を行ない
ながら決めるのが確実であり、その結果に基づいて酸価
を決定した。In order to satisfy these various properties, the acid value of the synthetic resin used in the toner should be determined within a practical range. In order to determine the appropriate acid value, it is reliable to determine it while actually performing development, and the acid value was determined based on the results.
特許出願代理人 古式 敬喜Patent application agent Takayoshi Koshiki
Claims (1)
分として用いることにより、ジャンピング機能を付与し
、染料及び顔料の混合により調色可能な、ジャンピ′ン
グ現像法に適する現像剤を得ることを特徴とした静電潜
像現像剤の製造法。By using a synthetic resin having a carboxyl group and an acid value of 5 to 30 as the main component, a developer suitable for the jumping development method is obtained, which has a jumping function and can be toned by mixing dyes and pigments. A method for producing an electrostatic latent image developer characterized by:
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP56213599A JPS58113944A (en) | 1981-12-26 | 1981-12-26 | Production of electrostatic latent image developer |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP56213599A JPS58113944A (en) | 1981-12-26 | 1981-12-26 | Production of electrostatic latent image developer |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS58113944A true JPS58113944A (en) | 1983-07-07 |
Family
ID=16641852
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP56213599A Pending JPS58113944A (en) | 1981-12-26 | 1981-12-26 | Production of electrostatic latent image developer |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS58113944A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS60120368A (en) * | 1983-12-05 | 1985-06-27 | Fuji Xerox Co Ltd | Single-component nonmagnetic developer |
JPS616656A (en) * | 1984-06-20 | 1986-01-13 | Toshiba Corp | Developer |
-
1981
- 1981-12-26 JP JP56213599A patent/JPS58113944A/en active Pending
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS60120368A (en) * | 1983-12-05 | 1985-06-27 | Fuji Xerox Co Ltd | Single-component nonmagnetic developer |
JPS616656A (en) * | 1984-06-20 | 1986-01-13 | Toshiba Corp | Developer |
JPH0642081B2 (en) * | 1984-06-20 | 1994-06-01 | 株式会社東芝 | Developer |
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