JPH0488357A - Electrostatic photographic liquid developer - Google Patents
Electrostatic photographic liquid developerInfo
- Publication number
- JPH0488357A JPH0488357A JP2202433A JP20243390A JPH0488357A JP H0488357 A JPH0488357 A JP H0488357A JP 2202433 A JP2202433 A JP 2202433A JP 20243390 A JP20243390 A JP 20243390A JP H0488357 A JPH0488357 A JP H0488357A
- Authority
- JP
- Japan
- Prior art keywords
- liquid developer
- weight
- parts
- toner
- solvent
- 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
- 239000007788 liquid Substances 0.000 title claims abstract description 22
- 239000002904 solvent Substances 0.000 claims abstract description 14
- 239000007787 solid Substances 0.000 claims abstract description 11
- 229920001296 polysiloxane Polymers 0.000 claims abstract description 10
- 239000002245 particle Substances 0.000 claims abstract description 3
- 238000001704 evaporation Methods 0.000 claims description 2
- 230000000704 physical effect Effects 0.000 abstract description 6
- 238000007599 discharging Methods 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- -1 acroyl group Chemical group 0.000 description 9
- 239000011347 resin Substances 0.000 description 9
- 229920005989 resin Polymers 0.000 description 9
- CNPVJWYWYZMPDS-UHFFFAOYSA-N 2-methyldecane Chemical compound CCCCCCCCC(C)C CNPVJWYWYZMPDS-UHFFFAOYSA-N 0.000 description 7
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 7
- 239000001993 wax Substances 0.000 description 7
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 6
- 229910052710 silicon Inorganic materials 0.000 description 6
- 239000010703 silicon Substances 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- 229920001577 copolymer Polymers 0.000 description 5
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 4
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 239000000178 monomer Substances 0.000 description 4
- 239000003921 oil Substances 0.000 description 4
- 239000004698 Polyethylene Substances 0.000 description 3
- 239000000049 pigment Substances 0.000 description 3
- 229920001225 polyester resin Polymers 0.000 description 3
- 239000004645 polyester resin Substances 0.000 description 3
- 229920000573 polyethylene Polymers 0.000 description 3
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
- 241000557626 Corvus corax Species 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 2
- 238000004040 coloring Methods 0.000 description 2
- GMSCBRSQMRDRCD-UHFFFAOYSA-N dodecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCOC(=O)C(C)=C GMSCBRSQMRDRCD-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 description 2
- UACSZOWTRIJIFU-UHFFFAOYSA-N hydroxymethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCO UACSZOWTRIJIFU-UHFFFAOYSA-N 0.000 description 2
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 2
- BKIMMITUMNQMOS-UHFFFAOYSA-N nonane Chemical compound CCCCCCCCC BKIMMITUMNQMOS-UHFFFAOYSA-N 0.000 description 2
- HMZGPNHSPWNGEP-UHFFFAOYSA-N octadecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)C(C)=C HMZGPNHSPWNGEP-UHFFFAOYSA-N 0.000 description 2
- 229920002545 silicone oil Polymers 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- OSNILPMOSNGHLC-UHFFFAOYSA-N 1-[4-methoxy-3-(piperidin-1-ylmethyl)phenyl]ethanone Chemical compound COC1=CC=C(C(C)=O)C=C1CN1CCCCC1 OSNILPMOSNGHLC-UHFFFAOYSA-N 0.000 description 1
- GTJOHISYCKPIMT-UHFFFAOYSA-N 2-methylundecane Chemical compound CCCCCCCCCC(C)C GTJOHISYCKPIMT-UHFFFAOYSA-N 0.000 description 1
- KGIGUEBEKRSTEW-UHFFFAOYSA-N 2-vinylpyridine Chemical compound C=CC1=CC=CC=N1 KGIGUEBEKRSTEW-UHFFFAOYSA-N 0.000 description 1
- DWDURZSYQTXVIN-UHFFFAOYSA-N 4-[(4-aminophenyl)-(4-methyliminocyclohexa-2,5-dien-1-ylidene)methyl]aniline Chemical compound C1=CC(=NC)C=CC1=C(C=1C=CC(N)=CC=1)C1=CC=C(N)C=C1 DWDURZSYQTXVIN-UHFFFAOYSA-N 0.000 description 1
- DBCAQXHNJOFNGC-UHFFFAOYSA-N 4-bromo-1,1,1-trifluorobutane Chemical compound FC(F)(F)CCCBr DBCAQXHNJOFNGC-UHFFFAOYSA-N 0.000 description 1
- IYHIFXGFKVJNBB-UHFFFAOYSA-N 5-chloro-2-[(2-hydroxynaphthalen-1-yl)diazenyl]-4-methylbenzenesulfonic acid Chemical compound C1=C(Cl)C(C)=CC(N=NC=2C3=CC=CC=C3C=CC=2O)=C1S(O)(=O)=O IYHIFXGFKVJNBB-UHFFFAOYSA-N 0.000 description 1
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
- 102100040440 Adenylate kinase isoenzyme 5 Human genes 0.000 description 1
- 101710168711 Adenylate kinase isoenzyme 5 Proteins 0.000 description 1
- VVAVKBBTPWYADW-UHFFFAOYSA-L Biebrich scarlet Chemical compound [Na+].[Na+].OC1=CC=C2C=CC=CC2=C1N=NC(C(=C1)S([O-])(=O)=O)=CC=C1N=NC1=CC=C(S([O-])(=O)=O)C=C1 VVAVKBBTPWYADW-UHFFFAOYSA-L 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- 235000000177 Indigofera tinctoria Nutrition 0.000 description 1
- SGVYKUFIHHTIFL-UHFFFAOYSA-N Isobutylhexyl Natural products CCCCCCCC(C)C SGVYKUFIHHTIFL-UHFFFAOYSA-N 0.000 description 1
- NHTMVDHEPJAVLT-UHFFFAOYSA-N Isooctane Chemical compound CC(C)CC(C)(C)C NHTMVDHEPJAVLT-UHFFFAOYSA-N 0.000 description 1
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 1
- 240000000111 Saccharum officinarum Species 0.000 description 1
- 235000007201 Saccharum officinarum Nutrition 0.000 description 1
- 239000004234 Yellow 2G Substances 0.000 description 1
- YFCGDEUVHLPRCZ-UHFFFAOYSA-N [dimethyl(trimethylsilyloxy)silyl]oxy-dimethyl-trimethylsilyloxysilane Chemical compound C[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)C YFCGDEUVHLPRCZ-UHFFFAOYSA-N 0.000 description 1
- 239000011668 ascorbic acid Substances 0.000 description 1
- 235000013871 bee wax Nutrition 0.000 description 1
- 239000012166 beeswax Substances 0.000 description 1
- 235000013868 candelilla wax Nutrition 0.000 description 1
- 239000004204 candelilla wax Substances 0.000 description 1
- 229940073532 candelilla wax Drugs 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 235000013869 carnauba wax Nutrition 0.000 description 1
- 239000004203 carnauba wax Substances 0.000 description 1
- ZLFVRXUOSPRRKQ-UHFFFAOYSA-N chembl2138372 Chemical compound [O-][N+](=O)C1=CC(C)=CC=C1N=NC1=C(O)C=CC2=CC=CC=C12 ZLFVRXUOSPRRKQ-UHFFFAOYSA-N 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- XCJYREBRNVKWGJ-UHFFFAOYSA-N copper(II) phthalocyanine Chemical compound [Cu+2].C12=CC=CC=C2C(N=C2[N-]C(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 XCJYREBRNVKWGJ-UHFFFAOYSA-N 0.000 description 1
- JVSWJIKNEAIKJW-UHFFFAOYSA-N dimethyl-hexane Natural products CCCCCC(C)C JVSWJIKNEAIKJW-UHFFFAOYSA-N 0.000 description 1
- FTZLWXQKVFFWLY-UHFFFAOYSA-L disodium;2,5-dichloro-4-[3-methyl-5-oxo-4-[(4-sulfonatophenyl)diazenyl]-4h-pyrazol-1-yl]benzenesulfonate Chemical compound [Na+].[Na+].CC1=NN(C=2C(=CC(=C(Cl)C=2)S([O-])(=O)=O)Cl)C(=O)C1N=NC1=CC=C(S([O-])(=O)=O)C=C1 FTZLWXQKVFFWLY-UHFFFAOYSA-L 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Substances CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 235000010985 glycerol esters of wood rosin Nutrition 0.000 description 1
- 229920000578 graft copolymer Polymers 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
- 229940097275 indigo Drugs 0.000 description 1
- COHYTHOBJLSHDF-UHFFFAOYSA-N indigo powder Natural products N1C2=CC=CC=C2C(=O)C1=C1C(=O)C2=CC=CC=C2N1 COHYTHOBJLSHDF-UHFFFAOYSA-N 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- VKPSKYDESGTTFR-UHFFFAOYSA-N isododecane Natural products CC(C)(C)CC(C)CC(C)(C)C VKPSKYDESGTTFR-UHFFFAOYSA-N 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 229940107698 malachite green Drugs 0.000 description 1
- FDZZZRQASAIRJF-UHFFFAOYSA-M malachite green Chemical compound [Cl-].C1=CC(N(C)C)=CC=C1C(C=1C=CC=CC=1)=C1C=CC(=[N+](C)C)C=C1 FDZZZRQASAIRJF-UHFFFAOYSA-M 0.000 description 1
- 150000002688 maleic acid derivatives Chemical class 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000012170 montan wax Substances 0.000 description 1
- JMXROTHPANUTOJ-UHFFFAOYSA-H naphthol green b Chemical compound [Na+].[Na+].[Na+].[Fe+3].C1=C(S([O-])(=O)=O)C=CC2=C(N=O)C([O-])=CC=C21.C1=C(S([O-])(=O)=O)C=CC2=C(N=O)C([O-])=CC=C21.C1=C(S([O-])(=O)=O)C=CC2=C(N=O)C([O-])=CC=C21 JMXROTHPANUTOJ-UHFFFAOYSA-H 0.000 description 1
- 239000000025 natural resin Substances 0.000 description 1
- CXQXSVUQTKDNFP-UHFFFAOYSA-N octamethyltrisiloxane Chemical compound C[Si](C)(C)O[Si](C)(C)O[Si](C)(C)C CXQXSVUQTKDNFP-UHFFFAOYSA-N 0.000 description 1
- 239000012860 organic pigment Substances 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical class OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- PYWVYCXTNDRMGF-UHFFFAOYSA-N rhodamine B Chemical compound [Cl-].C=12C=CC(=[N+](CC)CC)C=C2OC2=CC(N(CC)CC)=CC=C2C=1C1=CC=CC=C1C(O)=O PYWVYCXTNDRMGF-UHFFFAOYSA-N 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- JOUDBUYBGJYFFP-FOCLMDBBSA-N thioindigo Chemical compound S\1C2=CC=CC=C2C(=O)C/1=C1/C(=O)C2=CC=CC=C2S1 JOUDBUYBGJYFFP-FOCLMDBBSA-N 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 235000019235 yellow 2G Nutrition 0.000 description 1
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野コ
本発明は、湿式電子写真複写機に用いられる液体現像剤
に関する。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a liquid developer used in a wet-type electrophotographic copying machine.
[従来の技術]
従来、熱ロール定着ロール用の液体現像剤として、特開
昭Ei3−301968.301967.30197g
、301969、特開平64−50062.50063
.50064.50065.5006B 、50087
.52167.142560.142581などがある
。これらは脂肪族炭化水素が主成分の担体液のため、そ
の脂肪族炭化水素のガスが複写機外へ排出される結果、
狭い室内での作業時あるいは連続複写時に不快臭を発生
する等環境への悪影響があった。[Prior Art] Conventionally, as a liquid developer for a heat roll fixing roll, JP-A-Sho Ei3-301968.301967.30197g
, 301969, JP 64-50062.50063
.. 50064.50065.5006B, 50087
.. 52167.142560.142581, etc. These are carrier liquids mainly composed of aliphatic hydrocarbons, and as a result of the aliphatic hydrocarbon gas being discharged outside the copying machine,
This had negative effects on the environment, such as producing an unpleasant odor when working in a small room or when making continuous copies.
他方、画像品質、省エネルギーの面から湿式トナーの定
着には熱圧ロールの使用か有効であるが、従来の湿式ト
ナーは、低粘度、低 率の材料を使用してきたため、
凝集力が弱く、熱ロール上にいわゆるオフセット現象を
生じやすく、実際の複写機のロール温度が不安定である
ため、画像品質も不安定なものであった。On the other hand, from the viewpoint of image quality and energy saving, it is effective to use a hot pressure roll for fixing wet toner, but conventional wet toner has used materials with low viscosity and low ratio.
The cohesive force is weak, so-called offset phenomenon tends to occur on the heated roll, and since the roll temperature of an actual copying machine is unstable, the image quality is also unstable.
また、トナー層と定着ロールとの離型性を上げるためシ
リコンオイルの塗布が必要であったが、そのために複写
機複雑になったり、消耗品点数が増すなどといった問題
があった。Furthermore, in order to improve the releasability between the toner layer and the fixing roll, it was necessary to apply silicone oil, but this caused problems such as making the copying machine more complicated and increasing the number of consumables.
[発明が解決しようとする課題]
本発明は、こうした実情に鑑み、連続複写を行っても不
快臭あるいはオフセット現象の発生がなく、また定着ロ
ールへのオイル塗布を省略することができる液体現像剤
を提供することを目的とするものである。[Problems to be Solved by the Invention] In view of these circumstances, the present invention provides a liquid developer that does not cause unpleasant odor or offset phenomenon even when continuous copying is performed, and that can omit oil application to the fixing roll. The purpose is to provide the following.
[課題を解決するための手段]
本発明者らは前記した課題を解決すべく鋭意検討した結
果、シリコーン系溶剤を含む液体現像剤中のトナーの特
定の物性値を制御することが有効であることを知見し、
本発明に至った。[Means for Solving the Problems] As a result of intensive studies by the present inventors to solve the above problems, it has been found that it is effective to control specific physical property values of toner in a liquid developer containing a silicone solvent. I found out that
This led to the present invention.
すなわち、本発明は、少なくともシリコーン系溶剤を含
む高抵抗誘電体の担体液中にトナー粒子を分散してなる
静電写真用液体現像剤において、(1)固形分濃度がi
o、0wt%のときに100℃におする粘度が1〜50
cpであること、(2)担体液をすべて蒸発させた後の
乾燥固形物の弾性率が100〜180℃の間で10’
〜107dyne/c♂を示すこと、(3)前記乾燥固
形物の臨界表面張力か18〜36 dyne/(2)で
あることを特徴とする静電写真用液体現像剤である。That is, the present invention provides an electrostatographic liquid developer comprising toner particles dispersed in a high-resistance dielectric carrier liquid containing at least a silicone solvent, (1) a solid content concentration of i.
o, the viscosity at 100°C at 0 wt% is 1 to 50
cp, (2) the elastic modulus of the dry solid after evaporating all the carrier liquid is 10' between 100 and 180°C;
(3) The critical surface tension of the dry solid is 18 to 36 dyne/(2).
本発明の液体現像剤は、担体液としてシリコーン系溶剤
を含むものである。The liquid developer of the present invention contains a silicone solvent as a carrier liquid.
本発明に使用される前記シリコーン系の溶剤としては、
KF96 (信越シリコン) 、5H200SH344
(東しシリコン)、TSF451 (東芝シリコン)な
どが挙げられ、その他デカメチルテトラシロキサン、オ
クタメチルトリシロキサン等を使用してもよい。また、
シクロヘキサン、nヘキサン、n−へブタン、ローオク
タン、nノナン、イソオクタン、イソドデカン、リグロ
イン及びそれらの混合物などの石油系炭化水素(市販品
としてエクソンケミカル社製アイソパーE。The silicone-based solvent used in the present invention includes:
KF96 (Shin-Etsu Silicon), 5H200SH344
(Toshiba Silicon), TSF451 (Toshiba Silicon), etc. In addition, decamethyltetrasiloxane, octamethyltrisiloxane, etc. may be used. Also,
Petroleum hydrocarbons such as cyclohexane, n-hexane, n-hebutane, low-octane, n-nonane, isooctane, isododecane, ligroin, and mixtures thereof (commercially available products include Isopar E manufactured by Exxon Chemical Company).
G、H,L、に、Vやシェル石油社製シェルゾール71
、ソルッペツソ150、等がある)を適宜混合してもよ
い。転写溶剤を低減するために、担体液は10cst以
下、好ましくは3 est以下がよい。従って、市販シ
リコーン溶剤は各商品の内低粘度グレードが好ましい。G, H, L, V and Shell Sol 71 manufactured by Shell Oil Co.
, Solupetsuso 150, etc.) may be mixed as appropriate. To reduce transfer solvent, the carrier liquid should be less than 10 cst, preferably less than 3 cst. Therefore, commercially available silicone solvents are preferably of low viscosity grade.
上記担体液中に分散されて本発明の液体現像剤に使用さ
れるトナーは、特定の物性値がある範囲内に保持されて
いなければならない。The toner dispersed in the carrier liquid and used in the liquid developer of the present invention must have specific physical properties within a certain range.
すなわち、(1)トナー濃度10vt%のときに100
℃における粘度が1〜50cp、好ましくは5〜25c
pであることが必要である。(2)非水溶媒を除去した
後の乾燥固体の弾性率が100〜180℃において、1
0 〜107dyne/ cllll、好ましくは10
〜106dyne/ cmであることが必要である。お
よび(3)前記乾燥固形物の臨界表面張力が18〜36
dyne/ ccn 、好ましくは25〜33 dy
ne/ cmであることが必要である。That is, (1) 100 when the toner concentration is 10vt%.
Viscosity at °C from 1 to 50 cp, preferably from 5 to 25 cp
It is necessary that p. (2) The elastic modulus of the dry solid after removing the nonaqueous solvent is 1 at 100 to 180°C.
0 to 107 dyne/cllll, preferably 10
~106 dyne/cm is required. and (3) the critical surface tension of the dry solid is 18 to 36.
dyne/ccn, preferably 25-33 dy
ne/cm.
本発明において、上記の各物性値は以下のようにして測
定したものである。In the present invention, each of the above physical property values was measured as follows.
粘度は、Reolllet r i e社製のReom
at30によって測定された塑性粘度の値を示す。The viscosity is Reom manufactured by Reollet Rie.
The values of plastic viscosity measured by at30 are shown.
弾性率の測定は、ReOmetrje社製DR8−20
0を用いて行った。また、臨界表面張力は、協和科学(
株)製の接触角計CA−D型を用いて測定した。The elastic modulus was measured using ReOmetrje DR8-20.
This was done using 0. In addition, the critical surface tension is determined by Kyowa Science (
It was measured using a contact angle meter model CA-D manufactured by Co., Ltd.
本発明に使用するトナーのため分散用樹脂としでは、
一般式
%式%
であられされるビニルモノマーAと
一般式
%式%
で表わされるビニルモノマー及びビニルピリジン、ビニ
ルピロリドン、エチレングリコールジメタクリレート、
スチレン、ジビニルベンゼン、ビニルトルエンより選ば
れるモノマーBの各一種づつもしくは、数種の共重合体
、グラフト共重合体があげられる。The dispersing resin for the toner used in the present invention includes vinyl monomer A expressed by the general formula %, vinyl monomer A expressed by the general formula %, vinyl pyridine, vinyl pyrrolidone, ethylene glycol dimethacrylate,
Examples include copolymers and graft copolymers of each type of monomer B selected from styrene, divinylbenzene, and vinyltoluene, or several types of monomers.
又、シリコン溶剤への分散性を上げるためにアクロイル
基を有するシリコン材料、信越シリコンのL S 40
80などを共重合させても良いし、同様に東亜合成化学
のAK−5、チッソのT M 0701゜FMO711
,FMO721,FMO725を使用しても良い。In addition, in order to improve dispersibility in silicone solvents, a silicone material with an acroyl group, Shin-Etsu Silicon's L S 40, is used.
80 etc. may be copolymerized, and similarly, Toagosei Chemical's AK-5 and Chisso's TM 0701°FMO711 may be copolymerized.
, FMO721, and FMO725 may also be used.
これらの着色材、樹脂、担体液をボールミル、キティー
ミル、ディスクミル、ピンミルなどの分散機に投入、分
散、混線を行う。These coloring materials, resins, and carrier liquids are put into a dispersing machine such as a ball mill, kitty mill, disk mill, or pin mill, and are dispersed and mixed.
本発明に使用できる着色材としては、プリンテックスV
、プリンテックスU1プリンテックスG1スペシャルブ
ラック15、スペシャルブラック4、スペシャルブラッ
ク4−B(以上デグサ社製)、三菱#44、#30.M
R−11、MA−100(以上三菱化成社製)、ラーベ
ン1035、ラーベン1252、二ニースペクトラ■(
以上コロンビアカーボン社製)、リーガル400,66
0、ブラックバール900 、1100,1300 、
モガールしく以上キャポット社製)などの無機顔料およ
びフタロシアニンブルー フタロシアニングリーン、ス
カイブルー ローダミンレーキ、マラカイトグリーンレ
ーキ、メチルバイオレットレーキ、ピーコックブルーレ
ーキ、ナフトールグリーンB1 トールレッド、リノー
ルファーストイエロー2G、パーマネントレツド4R,
ブリリアントファストスカーレット、ハンザイエロー、
ベンジジンイエロー リソールレッド、レーキレッドC
ル−キレ・ソドD、ブリリアントカーメン6B、パーマ
ネントレッドF5R,ビグメントスカーレット3Bイン
ジゴ、チオインジゴオイルピンクおよびボルドー10B
などの有機顔料があげられる。As a coloring material that can be used in the present invention, Printex V
, Printex U1 Printex G1 Special Black 15, Special Black 4, Special Black 4-B (manufactured by Degussa), Mitsubishi #44, #30. M
R-11, MA-100 (manufactured by Mitsubishi Kasei Corporation), Raven 1035, Raven 1252, Nini Spectra (
(manufactured by Columbia Carbon), Regal 400,66
0, Black Baal 900, 1100, 1300,
Inorganic pigments such as Mogul Shikoku Kapot) and phthalocyanine blue Phthalocyanine Green, Sky Blue Rhodamine Lake, Malachite Green Lake, Methyl Violet Lake, Peacock Blue Lake, Naphthol Green B1 Tall Red, Linole Fast Yellow 2G, Permanent Red 4R,
Brilliant Fast Scarlet, Hansa Yellow,
Benzidine Yellow, Risol Red, Lake Red C
Loukire Sodo D, Brilliant Carmen 6B, Permanent Red F5R, Pigment Scarlet 3B Indigo, Thioindigo Oil Pink and Bordeaux 10B
Organic pigments such as
以上の顔料を前記樹脂と、二本ロール、ニーダ−フラッ
シャ−などで混練、粉砕し、顔料を処理することができ
る。また、下記の樹脂を使用しても良い。The pigment can be treated by kneading and pulverizing the above pigment with the resin using a two-roll machine, a kneader flasher, or the like. Further, the following resins may also be used.
イーストマンケミカル(Eastman Chemic
al)社N−10,N−11,N−12,N−14,N
−34,N−45,C−1DC−13,C−15,C−
16,E−1o、 E−11,E−12,E−14三井
石油化学社
110P、 220P、 220MP 、 820MP
、 410MP、 210MP。Eastman Chemical
al) Company N-10, N-11, N-12, N-14, N
-34,N-45,C-1DC-13,C-15,C-
16, E-1o, E-11, E-12, E-14 Mitsui Petrochemical Co., Ltd. 110P, 220P, 220MP, 820MP
, 410MP, 210MP.
310MP 、 405MP 、 200P、 420
2E 、 4053E三洋化成社
131P、 151P、 1BIP、 171P、 E
300. E250Pサゾール社
旧、 H2,Al、 A2. A3. A4バスフ(B
ASP)社
OA WAX、 A WAX
ベトロライト(Petrolite)社バレコ(BAR
ECO) 500 、バレコ(BARECO)2000
、 E−730、E−2018,E−2020,E−1
040、ペトロナバ(Petronaba) C,ペト
ロナバ(Petronaba)C−38、ベトロナバ(
Petronaba)C−400、ベトロナバ(Pet
ronaba)C−7500ヘキスト(Hoechst
)社
PE580 、 PE130 、 PED121. P
ED136. PED153ユニオンカーバイド社
DYNI、 DYNP、 DYNH,DYNJ、 DY
NKモンサンド社
オルシン(ORUZON) 805 、705 、50
デュポン社
アラトン(ALAT)TON) 3. 10.12.1
4.1B、 20゜アライドケミカル社
ACポリエチレン6、8A、 615
三井ポリケミ力ル社
エバフレックス 150.210 、220 、250
。310MP, 405MP, 200P, 420
2E, 4053E Sanyo Chemical Co., Ltd. 131P, 151P, 1BIP, 171P, E
300. E250P Sasol former, H2, Al, A2. A3. A4 bass (B
ASP) company OA WAX, A WAX Petrolite company Bareco (BAR)
ECO) 500, BARECO 2000
, E-730, E-2018, E-2020, E-1
040, Petronaba C, Petronaba C-38, Petronaba (
Petronaba) C-400, Petronaba (Pet
ronaba) C-7500 Hoechst
) company PE580, PE130, PED121. P
ED136. PED153 Union Carbide DYNI, DYNP, DYNH, DYNJ, DY
NK Monsando ORUZON 805, 705, 50
DuPont ALATTON) 3. 10.12.1
4.1B, 20゜Allied Chemical AC polyethylene 6, 8A, 615 Mitsui Polychemical Co., Ltd. Evaflex 150.210, 220, 250
.
260 、310 、360 、410 、420 、
450 、480 。260, 310, 360, 410, 420,
450, 480.
550 、560
などの合成ポリエチレン、ポリプロピレン及びその変成
したもの、カルナバワックス、モンタンワックス、キャ
ンデリラワックス、シュガーケーンワックス、オーリキ
ュリーワックス、蜜蝋、木蝋、ヌカ蝋などの天然ワック
ス、エステルガム、硬化ロジンなどの天然樹脂、天然樹
脂変成マレイン酸樹脂、天然樹脂変成フェノール樹脂、
天然樹脂変成ポリエステル樹脂、天然樹脂変成ペンタエ
リスリトール樹脂、エポキシ樹脂などの天然樹脂変成硬
化樹脂。Synthetic polyethylene such as 550 and 560, polypropylene and modified products thereof, natural waxes such as carnauba wax, montan wax, candelilla wax, sugar cane wax, auricule wax, beeswax, wood wax, bran wax, ester gum, hardened rosin, etc. natural resins, natural resin-modified maleic acid resins, natural resin-modified phenolic resins,
Natural resin-modified hardening resins such as natural resin-modified polyester resin, natural resin-modified pentaerythritol resin, and epoxy resin.
[実施例] 以下に実施例を挙げて本発明をさらに詳細に説明する。[Example] The present invention will be explained in more detail with reference to Examples below.
実施例1
ポリ酢酸ビニル樹脂 50重量部ラウリ
ルメタアクリレート/メチルメ
タアクリレート/メタクリル酸/グリ
シジルメタアクリレート(80/101515)共重合
体アイソ式−H20%溶液 100重量部アイソパー
H(EXXSON社)200重量部をボールミルに入れ
セ4時間分散後、さらにアイソパーHを300重量部加
え、1時間分散し、これを濃縮トナーとした。これを2
00gとりKF96(信越シリコン製1粘度3est)
151に希釈し、現像剤とした。Example 1 Polyvinyl acetate resin 50 parts by weight Lauryl methacrylate/methyl methacrylate/methacrylic acid/glycidyl methacrylate (80/101515) copolymer iso-H 20% solution 100 parts by weight Isopar H (EXXSON) 200 parts by weight After dispersing for 4 hours in a ball mill, 300 parts by weight of Isopar H was further added and dispersed for 1 hour to obtain a concentrated toner. This 2
00g KF96 (Shin-Etsu Silicon 1 viscosity 3est)
The solution was diluted to 151% and used as a developer.
実施例2
アミノ変性ポリエステル樹脂 57重量部250
p (三洋化成ポリエチレン) 8重量部MA6
0 (三菱化成カーボンブラック)35重量部をフラッ
シャ−で混練後粉砕した。Example 2 Amino-modified polyester resin 57 parts by weight 250
p (Sanyo Chemical Polyethylene) 8 parts by weight MA6
35 parts by weight of 0 (Mitsubishi Kasei Carbon Black) were kneaded with a flasher and then pulverized.
前記粉砕物 60重量部ステア
リルメタクリレート/メチルメ
タクリレート/メタクリル酸/ヒドロ
キシメチルメタクリレート(85/7/4/4)共重合
体アイソパーHIO%溶液 200重量部アイソパー
H100重量部
以下実施例1と同様に実施して現像剤とした。The above pulverized product 60 parts by weight Stearyl methacrylate/methyl methacrylate/methacrylic acid/hydroxymethyl methacrylate (85/7/4/4) copolymer Isopar HIO% solution 200 parts by weight Isopar H 100 parts by weight or less It was used as a developer.
実施例3
E−10(イーストマンケミカル)25重量部0AWA
X (BASF社)30重量部をフラッシャ−で混線
後粉砕した。Example 3 E-10 (Eastman Chemical) 25 parts by weight 0AWA
30 parts by weight of X (BASF) was mixed with a flasher and then pulverized.
前記粉砕物 60重量部ステア
リルメタクリレート/メチルメ
タクリレート/メタクリル酸/ヒドロ
キシメチルメタクリレート(85/7/4/4)共重合
体アイソパーHIO%溶液 200重量部アイソパー
H100重量部
以下実施例1と同様に実施して、現像剤とした。The above pulverized product 60 parts by weight Stearyl methacrylate/methyl methacrylate/methacrylic acid/hydroxymethyl methacrylate (85/7/4/4) copolymer Isopar HIO% solution 200 parts by weight Isopar H 100 parts by weight or less This was used as a developer.
実施例4
エバフレックス21O(三井ポリケミカル)50重量部
PE130 (Hoechst)
50重量部ラウリルメタアクリレート/メチルメ
タアクリレート/メタクリル酸/グリ
シジルメタアクリレート(80/101515)共重合
体アイソ式−H20%溶液 100重量部アイソパー
H(EXXSON社)200重量部をボールミルに入れ
24時間分散後、さらにアイソパーHを300重量部加
え、1時間分散し、これを濃縮トナーとした。これを2
00gとりKF96(信越シリコン製、粘度3cst)
・・・・・・に希釈現像剤とした。Example 4 Evaflex 21O (Mitsui Polychemical) 50 parts by weight PE130 (Hoechst)
50 parts by weight lauryl methacrylate/methyl methacrylate/methacrylic acid/glycidyl methacrylate (80/101515) copolymer iso-H 20% solution 100 parts by weight 200 parts by weight of Isopar H (EXXSON) were placed in a ball mill and dispersed for 24 hours. After that, 300 parts by weight of Isopar H was further added and dispersed for 1 hour to obtain a concentrated toner. This 2
00g KF96 (manufactured by Shin-Etsu Silicon, viscosity 3cst)
A diluted developer was prepared.
比較例1
実施例2においてポリエステル樹脂の分子量を約半分に
調整した樹脂を使用し、250pを8重量部から、28
重量部として一実施した。Comparative Example 1 Using a resin in which the molecular weight of the polyester resin in Example 2 was adjusted to about half, 250p was added from 8 parts by weight to 28 parts by weight.
It was carried out as parts by weight.
これら試作トナーを所定の方法により物性を測定した。The physical properties of these trial toners were measured by a predetermined method.
また、(株)リコー製CT −5085の定着部を(株
)リコー製F T −4550の定着ローラ一対を取り
付けて改造した複写機を用いて、定着特性の評価を行な
った。各々のトナーの物性と、定着ローラー上にオフセ
ットの発生しない非オフセット温度域は表−1に示す通
りである。但し、定着ローラー周辺からはオイル塗布用
の部材1機構は取り除いである。Further, the fixing characteristics were evaluated using a copying machine in which the fixing unit of Ricoh Co., Ltd. CT-5085 was modified by attaching a pair of Ricoh Co., Ltd. FT-4550 fixing rollers. Table 1 shows the physical properties of each toner and the non-offset temperature range in which no offset occurs on the fixing roller. However, the oil application member 1 mechanism is removed from the vicinity of the fixing roller.
以上の結果より、本発明によりオフセット現像を示さな
い熱ローラ定着可能な広範囲の温度幅が得られ、熱ロー
ラ定着が可能であることがわかる。From the above results, it can be seen that according to the present invention, a wide temperature range in which offset development is not caused and heat roller fixing is possible can be obtained, and heat roller fixing is possible.
また、実施例1のトナーをシリコンオイルの代りにアイ
ソパーHを用いて希釈し、現像剤として用い連続コピー
を行なったところ、密閉された室内で溶剤濃度は300
〜360 ppmであったが、実施例1の現像剤では同
様の実験で80〜150ppmと半減し不快臭もなかっ
た。Furthermore, when the toner of Example 1 was diluted with Isopar H instead of silicone oil and used as a developer for continuous copying, the solvent concentration was 300% in a sealed room.
However, in the developer of Example 1, the amount was reduced by half to 80 to 150 ppm in a similar experiment, and there was no unpleasant odor.
[発明の効果]
以上説明したように、本発明の液体現像剤を使用すると
きは、熱ロールへのオイルの塗布、供給を要せず、その
ための装置を省略することかできるので複写機をそれだ
け簡略化することができる。[Effects of the Invention] As explained above, when using the liquid developer of the present invention, it is not necessary to apply or supply oil to the heat roll, and the equipment for this purpose can be omitted, so that the copying machine can be easily used. It can be simplified accordingly.
またホットオフセットを防止すると共に不快臭を発する
溶剤の排出量も低減することができる。Furthermore, it is possible to prevent hot offset and reduce the amount of solvent emitted that gives off an unpleasant odor.
Claims (1)
液中にトナー粒子を分散してなる静電写真用液体現像剤
において、 (1)固形分濃度が10.0wt%のときに100℃に
おける粘度が1〜50cpであること、 (2)担体液をすべて蒸発させた後の乾燥固形物の弾性
率が100〜180℃の間で10^4〜10^7dyn
e/cm^2を示すこと、 (3)前記乾燥固形物の臨界表面張力が18〜36dy
ne/cmであること を特徴とする静電写真用液体現像剤。[Scope of Claims] An electrostatographic liquid developer comprising toner particles dispersed in a high-resistance dielectric carrier liquid containing at least a silicone solvent: (1) When the solid content concentration is 10.0 wt%; (2) The elastic modulus of the dry solid after evaporating all the carrier liquid is 10^4 to 10^7 dyn at 100 to 180 °C.
(3) The critical surface tension of the dry solid is 18 to 36 dy.
A liquid developer for electrostatic photography, characterized in that ne/cm.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2202433A JP3034563B2 (en) | 1990-08-01 | 1990-08-01 | Liquid developer for electrostatic photography |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2202433A JP3034563B2 (en) | 1990-08-01 | 1990-08-01 | Liquid developer for electrostatic photography |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH0488357A true JPH0488357A (en) | 1992-03-23 |
JP3034563B2 JP3034563B2 (en) | 2000-04-17 |
Family
ID=16457442
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2202433A Expired - Fee Related JP3034563B2 (en) | 1990-08-01 | 1990-08-01 | Liquid developer for electrostatic photography |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP3034563B2 (en) |
-
1990
- 1990-08-01 JP JP2202433A patent/JP3034563B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
JP3034563B2 (en) | 2000-04-17 |
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