JPH02199462A - Powder ink - Google Patents
Powder inkInfo
- Publication number
- JPH02199462A JPH02199462A JP1020112A JP2011289A JPH02199462A JP H02199462 A JPH02199462 A JP H02199462A JP 1020112 A JP1020112 A JP 1020112A JP 2011289 A JP2011289 A JP 2011289A JP H02199462 A JPH02199462 A JP H02199462A
- Authority
- JP
- Japan
- Prior art keywords
- styrene
- powder ink
- resin
- copolymer
- binder resin
- 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
- 239000000843 powder Substances 0.000 title claims abstract description 39
- 229920005989 resin Polymers 0.000 claims abstract description 32
- 239000011347 resin Substances 0.000 claims abstract description 32
- 239000011230 binding agent Substances 0.000 claims abstract description 17
- 239000004020 conductor Substances 0.000 claims abstract description 15
- 239000000126 substance Substances 0.000 claims description 9
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 abstract description 56
- 239000012188 paraffin wax Substances 0.000 abstract description 10
- 239000003822 epoxy resin Substances 0.000 abstract description 5
- 229920000647 polyepoxide Polymers 0.000 abstract description 5
- 239000004925 Acrylic resin Substances 0.000 abstract description 3
- 229920000178 Acrylic resin Polymers 0.000 abstract description 2
- 239000006229 carbon black Substances 0.000 abstract description 2
- 229920001577 copolymer Polymers 0.000 description 29
- 239000000976 ink Substances 0.000 description 29
- 239000001993 wax Substances 0.000 description 14
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 12
- 239000002245 particle Substances 0.000 description 10
- 235000019271 petrolatum Nutrition 0.000 description 7
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 6
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 6
- SOGAXMICEFXMKE-UHFFFAOYSA-N alpha-Methyl-n-butyl acrylate Natural products CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 5
- -1 isobutyl maleic acid Chemical compound 0.000 description 5
- 229920006243 acrylic copolymer Polymers 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 239000004359 castor oil Substances 0.000 description 2
- 235000019438 castor oil Nutrition 0.000 description 2
- 239000006258 conductive agent Substances 0.000 description 2
- 125000001664 diethylamino group Chemical group [H]C([H])([H])C([H])([H])N(*)C([H])([H])C([H])([H])[H] 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000012170 montan wax Substances 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- 239000005416 organic matter Substances 0.000 description 2
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 229920001909 styrene-acrylic polymer Polymers 0.000 description 2
- 229920002818 (Hydroxyethyl)methacrylate Polymers 0.000 description 1
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- 229920002126 Acrylic acid copolymer Polymers 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 239000004166 Lanolin Substances 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- 240000007594 Oryza sativa Species 0.000 description 1
- 235000007164 Oryza sativa Nutrition 0.000 description 1
- 239000002033 PVDF binder Substances 0.000 description 1
- 239000004264 Petrolatum Substances 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 229920001328 Polyvinylidene chloride Polymers 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 229920006322 acrylamide copolymer Polymers 0.000 description 1
- 125000005396 acrylic acid ester group Chemical group 0.000 description 1
- 229920002877 acrylic styrene acrylonitrile Polymers 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 235000013871 bee wax Nutrition 0.000 description 1
- 239000012166 beeswax Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000004204 candelilla wax Substances 0.000 description 1
- 235000013868 candelilla wax Nutrition 0.000 description 1
- 229940073532 candelilla wax Drugs 0.000 description 1
- 239000004203 carnauba wax Substances 0.000 description 1
- 235000013869 carnauba wax Nutrition 0.000 description 1
- 239000012461 cellulose resin Substances 0.000 description 1
- 238000004581 coalescence Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 229920006037 cross link polymer Polymers 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- MYRTYDVEIRVNKP-UHFFFAOYSA-N divinylbenzene Substances C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- IUJAMGNYPWYUPM-UHFFFAOYSA-N hentriacontane Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC IUJAMGNYPWYUPM-UHFFFAOYSA-N 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 235000019388 lanolin Nutrition 0.000 description 1
- 229940039717 lanolin Drugs 0.000 description 1
- 239000006247 magnetic powder Substances 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000004200 microcrystalline wax Substances 0.000 description 1
- 235000019808 microcrystalline wax Nutrition 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- LSWADWIFYOAQRZ-UHFFFAOYSA-N n-(ethoxymethyl)prop-2-enamide Chemical compound CCOCNC(=O)C=C LSWADWIFYOAQRZ-UHFFFAOYSA-N 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 235000019809 paraffin wax Nutrition 0.000 description 1
- 229940066842 petrolatum Drugs 0.000 description 1
- 239000012169 petroleum derived wax Substances 0.000 description 1
- 235000019381 petroleum wax Nutrition 0.000 description 1
- 229920006122 polyamide resin Polymers 0.000 description 1
- 229920001230 polyarylate Polymers 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920005668 polycarbonate resin Polymers 0.000 description 1
- 239000004431 polycarbonate resin Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920002620 polyvinyl fluoride Polymers 0.000 description 1
- 239000005033 polyvinylidene chloride Substances 0.000 description 1
- 229920002981 polyvinylidene fluoride Polymers 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000001694 spray drying Methods 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 150000003440 styrenes Chemical class 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
- 229910000859 α-Fe Inorganic materials 0.000 description 1
Landscapes
- Developing Agents For Electrophotography (AREA)
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野]
本発明は、画像形成装置に使用される粉体インクの内、
特に導電性の粉体インクに関する。DETAILED DESCRIPTION OF THE INVENTION [Industrial Application Field] The present invention is directed to powder inks used in image forming apparatuses.
In particular, it relates to conductive powder ink.
[従来の技術]
導電性の粉体インクとして、持分5’8−10743が
あり、定着性を良くする為に、結着樹脂の軟化点を規定
することで、粉体インクの溶融時の流動性を確保し、定
着温度を低下させている。[Prior Art] As a conductive powder ink, there is 5'8-10743, and in order to improve the fixing properties, the softening point of the binder resin is specified, and the flow when the powder ink is melted is controlled. properties and lowers the fixing temperature.
[発明が解決しようとする課題]
しかし、ここで提案された粉体インクは、導電性を確保
するための導電材の量が規定されるため、ブロッキング
を防止しつつ樹脂単体で低減できる溶融時の流動性に限
界がある。[Problems to be Solved by the Invention] However, in the powder ink proposed here, since the amount of conductive material is specified to ensure conductivity, the amount of melting time that can be reduced by the resin alone while preventing blocking is has limited liquidity.
そこで、本発明は、これら問題点を解決したものであっ
て、その目的は、必要とする導電性を確保しつつ、さら
に定着性を改善した粉体インクを提供することにある。SUMMARY OF THE INVENTION The present invention has been made to solve these problems, and an object of the present invention is to provide a powder ink that has improved fixability while ensuring the necessary conductivity.
[課題を解決するための手段]
本発明の粉体インクは、導電材、結着樹脂により構成さ
れる粉体インクにおいて、結着樹脂と溶解度パラメータ
ーが、結着樹脂と1以上異なる有機物を内添し、さらに
、導電材が結着樹脂に主として分散されていることを特
徴とする。[Means for Solving the Problems] The powder ink of the present invention is composed of a conductive material and a binder resin, and contains an organic substance whose solubility parameter differs from the binder resin by one or more. Additionally, the present invention is further characterized in that the conductive material is mainly dispersed in the binder resin.
[作用]
本発明の上記構成によれば、導電材は、添加された有機
物にほとんど分散されないので、結着樹脂に対する導電
材量の比が有機物の内添により増加することで導電材間
の距離が狭くなり、粉体インクの導電性が確保されるも
のと考えられる。また、溶融時の粘性は、有機物の粘度
が、排除された導電材分散系の粘度より低いために低下
するものと考えられる。[Function] According to the above structure of the present invention, since the conductive material is hardly dispersed in the added organic matter, the distance between the conductive materials is increased by increasing the ratio of the amount of the conductive material to the binder resin due to the internal addition of the organic matter. It is thought that the conductivity of the powder ink is ensured by narrowing the area. Further, it is thought that the viscosity during melting is reduced because the viscosity of the organic substance is lower than the viscosity of the excluded conductive material dispersion system.
[実施例] 以下、実施例により本発明の詳細な説明する。[Example] Hereinafter, the present invention will be explained in detail with reference to Examples.
本発明の粉体インクに使用される結着樹脂として、公知
のポリスチレン及びその共重合体、たとえば、水素添加
スチレン樹脂、スチレン・イソブチレン共重合体、スチ
レン・ブタジェン共重合体、ABS樹脂、 ASA樹脂
、 As樹脂、 AASAs樹脂C8樹脂、ABS樹脂
、スチレン・Pクロロスチレン共重合体、−スチレン・
プロピレン共重合体、スチレン・ブタジェン架橋ポリマ
ー スチレン・ブタジェン・塩素化パラフィン共重合体
、スチレン・アリル・アルコール共重合体、スチレン・
ブタジェンゴムエマルジョン、スチレン、マレイン酸エ
ステル共重合体、スチレン・イソブチレン共重合体、ス
チレン・無水マレイン酸共重合体、アクリレート系樹脂
あるいはメタアクリレート系樹脂及びその共重合体、ス
チレン・アクリル系樹脂及びその共重合体、たとえば、
スチレン・アクリル共重合体、スチレン・ジエチルアミ
ノ・エチルメタアクリレート共重合体、スチレン・ブタ
ジェン・アクリル酸エステル共重合体、スチレン・メチ
ルメタアクリレート共重合体、スチレン・n・ブチルメ
タアクリレート共重合体、スチレン・ジエチルアミノ・
エチルメタアクリレート共重合体、スチレン・メチルメ
タアクリレートn−ブチルアクリレート共重合体、スチ
レン・メチルメタアクリレート・ブチルアリレート・N
−(エトキシメチル)アクリルアミド共重合体、スチレ
ン・グリシジルメタアクリレート共重合体、スチレン・
ブタジェン・ジメチル・アミノエチルメタアクリレート
共重合体、スチレン・アクリル酸エステル・マレイン酸
エステル共重合体、スチレン・メタアクリル酸メチル・
アクリル酸2−エチルヘキシル共重合体、スチレン・n
−ブチルアリレート・エチルグリコールメタアクリレー
ト共重合体、スチレン°n−ブチルメタアクリレート・
アクリル酸共重合体、スチレン・n−ブチルメタアクリ
レート・無水マレイン酸共重合体、スチレン・ブチルア
クリレート・イソブチルマレイン酸ハーフエステル・ジ
ビニルベンゼン共重合体、ポリエステル及びその共重合
体、ポリエチレン及びその共重合体、エポキシ樹脂、シ
リコーン樹脂、ポリプロピレン及びその共重合体、ワッ
クス類、ポリビニルクロライド、ポリビニリデンクロラ
イド、ポリビニルフルオライド、ポリビニリデンフルオ
ライド、フッ素樹脂、ポリアミド樹脂、ポリビニールア
ルコール樹脂、ポリウレタン樹脂、ポリカーボネート樹
脂、セルロース樹脂、ボリアリレート樹脂、ブチラール
樹脂、ポリビニルブチラールが単独で、あるいは、複合
して使用される。さらに、結着樹脂にワックス状化合物
を添加して使用でき、キャンデリラワックス、カルナバ
ワックス、ライスワックス等の植物系天然ワックス、み
つろう、ラノリン等の動物系天然ワックス、モンタンワ
ックス、オシケライト等の鉱物系天然ワックス、パラフ
ィンワックス、マイクロクリスタリンワックス、ペトロ
ラタム等の天然石油ワックス、ポリエチレンワックス、
フィッシャー・トロプシュワックス等の合成炭化水素ワ
ックス、モンタンワックス誘導体、パラフィンワックス
誘導体等の変性ワックス、硬化ひまし油、硬化ひまし油
誘導体等の水素化ワックス、脂肪酸、酸アミド、エステ
ル、ケトン等の合成ワックスの中から選ばれるワックス
を1種、あるいは、2種以上をブレンドして用いること
ができる。As the binder resin used in the powder ink of the present invention, known polystyrene and copolymers thereof, such as hydrogenated styrene resin, styrene-isobutylene copolymer, styrene-butadiene copolymer, ABS resin, and ASA resin. , As resin, AASAs resin C8 resin, ABS resin, styrene/P-chlorostyrene copolymer, -styrene/
Propylene copolymer, styrene/butadiene crosslinked polymer Styrene/butadiene/chlorinated paraffin copolymer, styrene/allyl/alcohol copolymer, styrene/butadiene/chlorinated paraffin copolymer, styrene/butadiene/chlorinated paraffin copolymer,
Butadiene rubber emulsion, styrene, maleic ester copolymer, styrene/isobutylene copolymer, styrene/maleic anhydride copolymer, acrylate resin or methacrylate resin and its copolymer, styrene/acrylic resin, The copolymer, for example,
Styrene/acrylic copolymer, styrene/diethylamino/ethyl methacrylate copolymer, styrene/butadiene/acrylic ester copolymer, styrene/methyl methacrylate copolymer, styrene/n/butyl methacrylate copolymer, styrene・Diethylamino・
Ethyl methacrylate copolymer, styrene/methyl methacrylate n-butyl acrylate copolymer, styrene/methyl methacrylate/butyl arylate/N
-(Ethoxymethyl)acrylamide copolymer, styrene/glycidyl methacrylate copolymer, styrene/
Butadiene/dimethyl/aminoethyl methacrylate copolymer, styrene/acrylic acid ester/maleic ester copolymer, styrene/methyl methacrylate/
2-ethylhexyl acrylate copolymer, styrene/n
-Butyl arylate/ethyl glycol methacrylate copolymer, styrene °n-butyl methacrylate/
Acrylic acid copolymer, styrene/n-butyl methacrylate/maleic anhydride copolymer, styrene/butyl acrylate/isobutyl maleic acid half ester/divinylbenzene copolymer, polyester and its copolymer, polyethylene and its copolymer Coalescence, epoxy resin, silicone resin, polypropylene and its copolymers, waxes, polyvinyl chloride, polyvinylidene chloride, polyvinyl fluoride, polyvinylidene fluoride, fluororesin, polyamide resin, polyvinyl alcohol resin, polyurethane resin, polycarbonate resin , cellulose resin, polyarylate resin, butyral resin, and polyvinyl butyral may be used alone or in combination. Furthermore, wax-like compounds can be added to the binder resin, including plant-based natural waxes such as candelilla wax, carnauba wax, and rice wax, animal-based natural waxes such as beeswax and lanolin, and mineral-based waxes such as montan wax and osikerite. Natural wax, paraffin wax, microcrystalline wax, natural petroleum wax such as petrolatum, polyethylene wax,
Synthetic hydrocarbon waxes such as Fischer-Tropsch wax, modified waxes such as montan wax derivatives and paraffin wax derivatives, hydrogenated waxes such as hydrogenated castor oil and hydrogenated castor oil derivatives, and synthetic waxes such as fatty acids, acid amides, esters, and ketones. One type of selected wax or a blend of two or more types can be used.
また、本発明の粉体インクの導電材として公知のカーボ
ンブラックあるいは、各種の金属、金属酸化物、金属塩
等が、単独で、あるいは、組み合わせて使用される。Furthermore, carbon black, various metals, metal oxides, metal salts, etc., which are known as conductive materials for the powder ink of the present invention, may be used alone or in combination.
本発明の粉体インクに使用される有機物とじて前述の樹
脂、ワックス等が使用される。その際、結着樹脂と相溶
せず、導電材も分散させないために、溶解度パラメータ
ーとして知られる物質のモル当りの蒸発エネルギーをモ
ル容積で割った量の平方根が、前述の結着樹脂と、1以
上離れていると相溶しにくくなる。The organic substances used in the powder ink of the present invention include the aforementioned resins and waxes. At that time, since it is not compatible with the binder resin and does not disperse the conductive material, the solubility parameter, which is the square root of the evaporation energy per mole of the substance divided by the molar volume, is determined by the binder resin and the conductive material. If they are separated by 1 or more, they will be difficult to dissolve.
本発明の粉体インクは、上記物質の他にその流動性、定
着性等を損なわない程度に添加物を添加できる。添加物
としては、金属石鹸、ポリエチレングリコール等の分散
剤、Fe5O4、Fe20a、 Fe、 Cr、
Ni、 Co、フェライト等の磁性粉が単独あるい
は組み合わせて使用される。In addition to the above-mentioned substances, additives can be added to the powder ink of the present invention to the extent that their fluidity, fixability, etc. are not impaired. Additives include metal soaps, dispersants such as polyethylene glycol, Fe5O4, Fe20a, Fe, Cr,
Magnetic powders such as Ni, Co, and ferrite are used alone or in combination.
[実施例1コ
溶解度パラメーターが11.0[cal/cm2] 1
/2のエポキシ樹脂の0.2μmの微粒子90重量部、
溶解度パラメーターが8.5 [cal/Cm3]””
のスチレンオリゴマー90重量部、導電性カーボンブラ
ック4重量部をトルエン中に入れ、ヘンシェルミキサー
にかけた後、スプレードライ法により粒子形成、分級し
平均粒径10.2μmの粉体インクA1を作製した。ス
チレンオリゴマーの軟化点は85℃、エポキシ樹脂の軟
化点は95℃であり、粉体インクのバルク抵抗は、10
2ΩCm、回転粘度計で測定した、180℃の粘度は3
×102であった。[Example 1 solubility parameter is 11.0 [cal/cm2] 1
90 parts by weight of 0.2 μm fine particles of /2 epoxy resin,
Solubility parameter is 8.5 [cal/Cm3]""
90 parts by weight of styrene oligomer and 4 parts by weight of conductive carbon black were placed in toluene, mixed with a Henschel mixer, and then formed into particles by a spray drying method and classified to produce powder ink A1 having an average particle size of 10.2 μm. The softening point of styrene oligomer is 85°C, the softening point of epoxy resin is 95°C, and the bulk resistance of powder ink is 10°C.
2ΩCm, the viscosity at 180℃ measured with a rotational viscometer is 3
It was ×102.
作製された、粉体インクA1を、電子写真方式の画像形
成装置を用いて画像形成を行った。このとき、A1は、
90℃の定着温度で定着され、光学温度(以下0.D、
値と称する。)1.6の画像が得られた。An image was formed using the produced powder ink A1 using an electrophotographic image forming apparatus. At this time, A1 is
It is fixed at a fixing temperature of 90°C, and the optical temperature (hereinafter referred to as 0.D,
It is called a value. ) 1.6 images were obtained.
[比較例1]
実施例1と同様の体積抵抗率を得るために、スチレンオ
リゴマー90重量部に対して、導電性カーボンブラック
を1.8重量部をトルエン中にいれ、ヘンシェルミキサ
ーにかけた後、スプレードライヤーにて粒子を形成して
、分級し平均粒径10.2μmの粉体インクB1を作製
した。体積抵抗率は102Ωcmであり、回転粘度計で
測定した、180℃の粘度は1. 6 X 103c、
p、 であった。[Comparative Example 1] In order to obtain the same volume resistivity as in Example 1, 1.8 parts by weight of conductive carbon black was added to 90 parts by weight of styrene oligomer in toluene, and then subjected to a Henschel mixer. Particles were formed using a spray dryer and classified to produce powder ink B1 having an average particle size of 10.2 μm. The volume resistivity is 102 Ωcm, and the viscosity at 180°C measured with a rotational viscometer is 1. 6 x 103c,
It was p.
作製された粉体インクB1を用いて、画像形成を行った
ところ、115℃の定着温度で定着され、0、D、値1
.6の画像が得られた。When an image was formed using the prepared powder ink B1, it was fixed at a fixing temperature of 115°C, and it had a value of 0, D, and 1.
.. 6 images were obtained.
以上のように、内添する樹脂を入れない場合と比較して
、同じ抵抗値を得るために必要な分量の導電剤を添加し
た場合は、定着に必要な温度が上昇することが判明した
。As described above, it has been found that when a conductive agent is added in an amount necessary to obtain the same resistance value, the temperature required for fixing increases compared to when no internally added resin is added.
[実施例2]
スチレンオリゴマーに、導電性カーボンブラックを4.
8wt%添加し、ヘンシェルミキサーにかけた後、3本
ロールミルで混練し冷却後粉砕、分級し平均粒径1.1
μmの微粉末を作製した。[Example 2] 4. Conductive carbon black was added to styrene oligomer.
8 wt% was added, put in a Henschel mixer, kneaded in a three-roll mill, cooled, crushed, and classified to have an average particle size of 1.1.
A micron-sized powder was produced.
この微粉末80重量部とエポキシ樹脂をさらに混合、混
線、粉砕し平均粒径10.9μmの粉体インクC1を作
製した。この時の体積抵抗率102ΩCmであった。1
80℃の粘度は8×103であった。80 parts by weight of this fine powder and an epoxy resin were further mixed, mixed, and pulverized to produce a powder ink C1 having an average particle size of 10.9 μm. The volume resistivity at this time was 102 ΩCm. 1
The viscosity at 80°C was 8 x 103.
粉体インクC1を用いて、画像形成を行ったとき、11
5℃の定着温度で定着され、○、D、値1゜6の画像が
得られた。When image formation was performed using powder ink C1, 11
The image was fixed at a fixing temperature of 5° C., and an image of ◯, D, and a value of 1°6 was obtained.
[比較例2]
スチレンオリゴマーに、導電性カーボンブラックを4.
2wt%添加し、ヘンシェルミキサーにかけた後、3本
ロールミルで混練し冷却後粉砕、分級し平均粒径10.
9μmの粉体インクD1を作製した。この時の体積抵抗
率102ΩCmであった。180℃の粘度はI X 1
0’であった。粉体インクD1を用いて、画像形成を行
ったとき、1300Cの定着温度で定着され、0.D、
値1.6の画像が得られた。[Comparative Example 2] 4.0% conductive carbon black was added to styrene oligomer.
2 wt% was added, put in a Henschel mixer, kneaded in a three-roll mill, cooled, crushed, and classified to have an average particle size of 10.
A 9 μm powder ink D1 was produced. The volume resistivity at this time was 102 ΩCm. The viscosity at 180°C is I x 1
It was 0'. When an image was formed using the powder ink D1, it was fixed at a fixing temperature of 1300C, and the image was formed at a temperature of 0. D.
An image with a value of 1.6 was obtained.
以上のように、内添する樹脂を入れない場合と比較して
、同じ抵抗値を得るために必要な分量の導電剤を添加し
た場合は、定着に必要な温度が上昇することが判明した
。As described above, it has been found that when a conductive agent is added in an amount necessary to obtain the same resistance value, the temperature required for fixing increases compared to when no internally added resin is added.
[実施例3]
溶解度パラメーターが9.5[cal/Cm3]5″の
スチレン、アクリル共重合体70重量部、導電性カーボ
ンブラック5重量部、および溶解度パラメーターが12
.7[cal/cm”コ1′2の平均粒径0・ 1μm
のパラフィンワックス10重量部をトルエン中に混合後
、混線・粉砕により、平均粒径1O15μmの粉体イン
クを作製した。スチレン、アクリル共重合体の軟化点は
105℃、パラフィンワックスの軟化点は90℃であり
、体積抵抗率は、102Ωcmであり、180℃に於け
る粘度は、9X103c、p、 であった。前記粉体
インクを画像形成させると、定着温度100℃で0、D
、値1.6の画像が形成された。[Example 3] Styrene with a solubility parameter of 9.5 [cal/Cm3]5'', 70 parts by weight of an acrylic copolymer, 5 parts by weight of conductive carbon black, and a solubility parameter of 12
.. 7 [cal/cm" average particle size of 1'2 0.1 μm
After mixing 10 parts by weight of paraffin wax in toluene, a powder ink having an average particle size of 1015 μm was prepared by mixing and crushing. The softening point of the styrene-acrylic copolymer was 105°C, the softening point of the paraffin wax was 90°C, the volume resistivity was 102 Ωcm, and the viscosity at 180°C was 9×103 c,p. When the powder ink is used to form an image, 0, D at a fixing temperature of 100°C.
, an image with a value of 1.6 was formed.
[比較例3]
溶解度パラメーターが9.5[cal/cm3]1′2
のスチレン、アクリル共重合体70重量部、導電性カー
ボンブラック5重量部、および溶解度パラメーターが1
0. 5 [c al/cm3コ1′2のパラフィンワ
ックス10重量部をトルエン中に混合後、混練・粉砕に
より、平均粒径10.5μmの粉体インクを作製した。[Comparative Example 3] Solubility parameter is 9.5 [cal/cm3] 1'2
of styrene, 70 parts by weight of acrylic copolymer, 5 parts by weight of conductive carbon black, and a solubility parameter of 1
0. A powder ink having an average particle size of 10.5 μm was prepared by mixing 10 parts by weight of paraffin wax of 5 cal/cm3 to 1'2 in toluene, and then kneading and pulverizing the mixture.
スチレン、アクリル共重合体の軟化点は105℃、パラ
フィンワックスの軟化点は90℃であり、体積抵抗率は
、102Ωcmであり、180℃に於ける粘度は、2X
10’c。The softening point of styrene-acrylic copolymer is 105°C, the softening point of paraffin wax is 90°C, the volume resistivity is 102Ωcm, and the viscosity at 180°C is 2X
10'c.
p、であった。前記粉体インクを画像形成させると、定
着温度160℃でO,D、 値1,6の画像が形成さ
れた。実施例3と比較して、同じ抵抗値での定着温度が
高くなっており、溶解度パラメーターが近いために、樹
脂同志相溶していることが光学顕微鏡により確認された
。It was p. When an image was formed using the powder ink, an image with O, D, and values of 1 and 6 was formed at a fixing temperature of 160°C. Compared to Example 3, the fixing temperature was higher at the same resistance value, and because the solubility parameters were similar, it was confirmed by an optical microscope that the resins were compatible with each other.
以上、いくつかの実施例について、本発明を説明してき
たが、互いに相溶しないその他の樹脂の組合せについて
も本発明が成立することは、以上の実施例から明白であ
ろう。Although the present invention has been described above with reference to several examples, it is clear from the above examples that the present invention can be applied to other combinations of resins that are not compatible with each other.
[発明の騎効果]
以上述べたように本発明によれば、導電材、結着樹脂に
より構成される粉体インクにおいて、結着樹脂と溶解度
パラメーターが、結着樹脂と1以上異なる有機物を内添
し、さらに、導電材が結着樹脂に主として分散されてい
ることにより、所定の抵抗値を得た場合により低温で定
着が可能となり、画像形成装置に使用すると、そのラン
ニングコストを低減できる。特に、熱転写方式にて画像
を形成する工程と、インクシートを再生する工程とを有
する画像形成方法で使用する粉体インクとして使用すれ
ば、大幅にランニングコストを低減させた画像形成装置
を提供できるようになる。ま−1ま
た、その他の画像形成装置に使用しても定着温度を低減
させる効果が認められた。例えば、電子写真方式を用い
たプリンター 複写機、ファクシミリ等の装置に使用す
る粉体インクとして応用できる。[Advantages of the Invention] As described above, according to the present invention, a powder ink composed of a conductive material and a binder resin contains an organic substance whose solubility parameter differs from that of the binder resin by one or more. Furthermore, since the conductive material is mainly dispersed in the binder resin, it is possible to fix at a lower temperature when a predetermined resistance value is obtained, and when used in an image forming apparatus, the running cost thereof can be reduced. In particular, if it is used as a powder ink for an image forming method that includes a step of forming an image using a thermal transfer method and a step of recycling an ink sheet, it is possible to provide an image forming apparatus with significantly reduced running costs. It becomes like this. Ma-1 Furthermore, the effect of reducing the fixing temperature was observed even when used in other image forming apparatuses. For example, it can be applied as a powder ink for use in devices such as printers, copiers, and facsimile machines that use electrophotography.
以 上 出願人 セイコーエプソン株式会社that's all Applicant: Seiko Epson Corporation
Claims (4)
おいて、結着樹脂と溶解度パラメーターが、結着樹脂と
1以上異なる有機物を内添し、さらに、導電材が結着樹
脂に主として分散されていることを特徴とする粉体イン
ク。(1) In a powder ink composed of a conductive material and a binder resin, an organic substance is internally added which has a solubility parameter different from that of the binder resin by one or more, and the conductive material is mainly dispersed in the binder resin. Powder ink characterized by:
^8Ωcmであることを特徴とする粉体インク。(2) The powder ink according to claim 1 has a volume resistivity of 10
Powder ink characterized by ^8Ωcm.
、1×10^4c.p.以下であることを特徴とする粉
体インク。(3) The organic substance according to claim 1 has a viscosity of 1×10^4 c. at 180°C. p. A powder ink characterized by:
の軟化点が70〜180℃であることを特徴とする粉体
インク。(4) A powder ink, characterized in that the binder resin according to claim 1 and the organic substance added therein have a softening point of 70 to 180°C.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1020112A JPH02199462A (en) | 1989-01-30 | 1989-01-30 | Powder ink |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1020112A JPH02199462A (en) | 1989-01-30 | 1989-01-30 | Powder ink |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH02199462A true JPH02199462A (en) | 1990-08-07 |
Family
ID=12018037
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1020112A Pending JPH02199462A (en) | 1989-01-30 | 1989-01-30 | Powder ink |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH02199462A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH09265206A (en) * | 1995-05-31 | 1997-10-07 | Canon Inc | Image forming method and thermal fixing method |
CN107390484A (en) * | 2017-08-29 | 2017-11-24 | 邯郸汉光办公自动化耗材有限公司 | Multifunctional colour ink powder and preparation method thereof and the method for thermal transfer printing |
-
1989
- 1989-01-30 JP JP1020112A patent/JPH02199462A/en active Pending
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH09265206A (en) * | 1995-05-31 | 1997-10-07 | Canon Inc | Image forming method and thermal fixing method |
CN107390484A (en) * | 2017-08-29 | 2017-11-24 | 邯郸汉光办公自动化耗材有限公司 | Multifunctional colour ink powder and preparation method thereof and the method for thermal transfer printing |
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