JPH0126065B2 - - Google Patents
Info
- Publication number
- JPH0126065B2 JPH0126065B2 JP20240782A JP20240782A JPH0126065B2 JP H0126065 B2 JPH0126065 B2 JP H0126065B2 JP 20240782 A JP20240782 A JP 20240782A JP 20240782 A JP20240782 A JP 20240782A JP H0126065 B2 JPH0126065 B2 JP H0126065B2
- Authority
- JP
- Japan
- Prior art keywords
- temperature
- hexanediol
- neopentyl glycol
- properties
- cleaning
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 238000004140 cleaning Methods 0.000 claims description 11
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 claims description 8
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 claims description 7
- 108091008695 photoreceptors Proteins 0.000 claims description 6
- 229920000728 polyester Polymers 0.000 claims description 5
- 229920006311 Urethane elastomer Polymers 0.000 claims description 2
- 229920001228 polyisocyanate Polymers 0.000 claims description 2
- 239000005056 polyisocyanate Substances 0.000 claims description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 claims 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims 1
- AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Natural products OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 claims 1
- 235000011037 adipic acid Nutrition 0.000 claims 1
- 239000001361 adipic acid Substances 0.000 claims 1
- 239000007795 chemical reaction product Substances 0.000 claims 1
- 229920003225 polyurethane elastomer Polymers 0.000 description 9
- 230000007062 hydrolysis Effects 0.000 description 7
- 238000006460 hydrolysis reaction Methods 0.000 description 7
- -1 Polyethylene adipate Polymers 0.000 description 6
- 229920000921 polyethylene adipate Polymers 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 4
- 230000000704 physical effect Effects 0.000 description 4
- 229920005862 polyol Polymers 0.000 description 4
- 150000003077 polyols Chemical class 0.000 description 4
- 230000002159 abnormal effect Effects 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 238000004132 cross linking Methods 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- 229920002635 polyurethane Polymers 0.000 description 3
- 239000004814 polyurethane Substances 0.000 description 3
- 239000002994 raw material Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
- 238000002425 crystallisation Methods 0.000 description 2
- 230000008025 crystallization Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 238000001746 injection moulding Methods 0.000 description 2
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- WNLRTRBMVRJNCN-UHFFFAOYSA-L adipate(2-) Chemical compound [O-]C(=O)CCCCC([O-])=O WNLRTRBMVRJNCN-UHFFFAOYSA-L 0.000 description 1
- 238000003776 cleavage reaction Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 125000005442 diisocyanate group Chemical group 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- ACCCMOQWYVYDOT-UHFFFAOYSA-N hexane-1,1-diol Chemical compound CCCCCC(O)O ACCCMOQWYVYDOT-UHFFFAOYSA-N 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 238000003672 processing method Methods 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G21/00—Arrangements not provided for by groups G03G13/00 - G03G19/00, e.g. cleaning, elimination of residual charge
- G03G21/0005—Arrangements not provided for by groups G03G13/00 - G03G19/00, e.g. cleaning, elimination of residual charge for removing solid developer or debris from the electrographic recording medium
- G03G21/0011—Arrangements not provided for by groups G03G13/00 - G03G19/00, e.g. cleaning, elimination of residual charge for removing solid developer or debris from the electrographic recording medium using a blade; Details of cleaning blades, e.g. blade shape, layer forming
- G03G21/0017—Details relating to the internal structure or chemical composition of the blades
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
Description
本発明は、電子写真複写機の潜像担体(感光
体)に形成された静電潜像にトナーを付着させ、
紙等のシートに転写後の感光体表面に残留するト
ナーを、感光体の表面と摺擦してクリーニングす
るに用いるブレードに関するものである。
クリーニングブレードに要求される性質として
は、機械的強度が大きいこと、諸特性の温度によ
る変化が小さいこと、耐加水分解性にすぐれてい
ること、耐オゾン性にすぐれていること等が挙げ
られる。
現在クリーニングブレードに使用されているポ
リウレタンのポリオール原料としては、ポリエチ
レンアジペートエステルが使用されているが、こ
のポリオールを使用したポリウレタンは上記の諸
性質を十分満足するものとは云い難い。特に温度
依存性が大きいことと、耐加水分解性が劣るため
に、それに起因する問題がかなり発生している。
電子写真複写機の内部は、露光ランプ、定着器
などから多量の熱が放出され、環境温度より5〜
20℃高温になつているのが普通であり、環境温度
は冬期の低湿低温から夏期の高湿高温まで温度で
0〜35℃程度変化するので、このような温度湿度
の変化により、ブレードの特性が大きく変化して
は実用上問題である。
ポリウレタンゴムが他の一般ゴムに較べ著しく
異なる点は、機械的、物理的性質が主に分子間凝
集力に移存しているため、温度が変ると諸特性が
大きく変わることである。特にソフトセグメント
を形成するポリオールの種類によつて温度依存性
が大きく支配される。
本発明はポリウレタンゴムのポリオール原料と
して1,6―ヘキサンジオールと、、ネオペンチ
ルグリコールをモル比で9/1〜5/5の割合で用いた
ポリウレタンを用いることにより上記の問題を解
決できるようにしたものである。
下記試験に用いたポリウレタンゴムは、ポリエ
チレンアジペート、1,6―ヘキサンジオールと
ネオペンチルグリコールとのアジペート及び、イ
ソシアネートとしてジフエニルメタン―4,4′―
ジイソシアネートを主原料とし、硬化剤として
1,4―ブタンジオール及びトリメチロールプロ
パンを併用した。
The present invention involves attaching toner to an electrostatic latent image formed on a latent image carrier (photoreceptor) of an electrophotographic copying machine,
This relates to a blade used to clean toner remaining on the surface of a photoreceptor after being transferred to a sheet such as paper by rubbing against the surface of the photoreceptor. Properties required of a cleaning blade include high mechanical strength, small changes in various properties due to temperature, excellent hydrolysis resistance, and excellent ozone resistance. Polyethylene adipate ester is currently used as a polyol raw material for polyurethane used in cleaning blades, but it is difficult to say that polyurethane using this polyol fully satisfies the above-mentioned properties. In particular, the large temperature dependence and poor hydrolysis resistance cause considerable problems. Inside an electrophotographic copying machine, a large amount of heat is emitted from the exposure lamp, fixing device, etc.
It is normal to have a high temperature of 20℃, and the environmental temperature varies from 0 to 35℃, from low humidity and low temperature in winter to high humidity and high temperature in summer, so these changes in temperature and humidity will affect the characteristics of the blade. It is a practical problem if the value changes significantly. Polyurethane rubber is significantly different from other general rubbers in that its mechanical and physical properties are mainly determined by intermolecular cohesive forces, so its properties change significantly when the temperature changes. In particular, the temperature dependence is largely controlled by the type of polyol forming the soft segment. The present invention solves the above problems by using polyurethane containing 1,6-hexanediol and neopentyl glycol in a molar ratio of 9/1 to 5/5 as polyol raw materials for polyurethane rubber. This is what I did. The polyurethane rubbers used in the following tests were polyethylene adipate, adipate of 1,6-hexanediol and neopentyl glycol, and diphenylmethane-4,4'- as the isocyanate.
Diisocyanate was used as the main raw material, and 1,4-butanediol and trimethylolpropane were used as curing agents.
【表】
上表のようにポリエチレンアジペートをベース
としたポリウレタンゴムは、反発弾性及びヤング
率の温度による変化が大きい。0℃では弾性が極
めて低く、感光体との密着性が問題となり、ヤン
グ率は常温に較べてかなり高いので、ブレート押
し付け圧が高くなつたり、接触角が設計値より大
きくなるので、異音が発生したり、クリーニング
不良につながつてしまう。50℃では反発弾性が高
くなりすぎ、バウンド現象や異音発生の原因とな
り、ヤング率の低下は、クリーニングブレードと
感光体との接触圧が小さくなり、腰力が低下する
ためトナーがクリーニングブレードと感光体の間
を通り抜け易くなる。
これに対し本発明の1,6―ヘキサンジオール
とネオペンチルグリコールをモル比で9/1〜5/5の
範囲で使用したポリウレタンゴムでは、反発弾性
及びヤング率の温度による変化がポリエチレンア
ジペートベースのポリウレタンゴムよりかなり小
さく、0〜50℃の範囲でほぼ満足すべき結果が得
られる。しかし1,6―ヘキサンジオールとネオ
ペンチルグリコールをモル比で3:7の割合で使
用したものでは50℃の反発弾性が高くなり異音を
発生した。またメチル基が増すため物性も悪くブ
レードとしては不適当である。
1,6―ヘキサンジオールのみを使用した場合
には、結晶化傾向が強く、その為に機械的強度は
十分に大きいが、低温特性が悪くなる。1,6―
ヘキサンジオールにネオペンチルグリコールを共
用することにより、メチル基の結晶化妨害効果を
生じて低温特性が改善され、温度による特性の変
化を小さくできる。
ポリウレタンゴムの他の欠点は、耐水性が悪い
ことである。ポリエチレンアジペートエステルを
ベースとしたウレタンゴムでは、クリーニングブ
レードが製造されてから、2〜4年経過したもの
は、使用条件によつても差があるが、加水分解が
進行していることが観察される。これは、主にエ
ステル結合の分子切断であつて、初めは序々に進
行するが、ある程度進行すると、加水分解により
生成した有機酸が促進剤となり、急速に劣化する
ためである。加水分解の進行したものは、夏期に
は軟化し、腰力が不足し充分なクリーニング作用
が得られず、冬期には結晶化のため弾性が低下し
クリーニング不充分となる。
耐加水分解性を比較するために、密閉容器の底
に少量の水を入れ、その上に試料を直接水と接触
しないように吊して、70℃に35日間保持した結
果、得られた物性の変化を下表に示す。[Table] As shown in the table above, polyurethane rubber based on polyethylene adipate has a large change in impact resilience and Young's modulus depending on temperature. At 0°C, elasticity is extremely low and adhesion with the photoreceptor becomes a problem. Young's modulus is much higher than at room temperature, so the plate pressing pressure becomes higher and the contact angle becomes larger than the designed value, causing abnormal noise. This can lead to poor cleaning. At 50 degrees Celsius, the repulsion elasticity becomes too high, causing bounce phenomena and abnormal noises.A decrease in Young's modulus is caused by a decrease in the contact pressure between the cleaning blade and the photoconductor, which reduces the back force, which causes the toner to contact the cleaning blade. It becomes easier to pass between the photoreceptors. On the other hand, in the polyurethane rubber of the present invention using 1,6-hexanediol and neopentyl glycol in a molar ratio of 9/1 to 5/5, the impact resilience and Young's modulus change with temperature compared to that of the polyethylene adipate-based polyurethane rubber. It is considerably smaller than polyurethane rubber, and almost satisfactory results can be obtained in the range of 0 to 50°C. However, when 1,6-hexanediol and neopentyl glycol were used in a molar ratio of 3:7, the impact resilience at 50°C was high and an abnormal noise was generated. Furthermore, due to the increased number of methyl groups, the physical properties are poor and it is unsuitable for blades. When only 1,6-hexanediol is used, it has a strong tendency to crystallize and therefore has a sufficiently high mechanical strength, but its low temperature properties deteriorate. 1,6-
By using neopentyl glycol in combination with hexanediol, the crystallization effect of the methyl group is produced, improving low-temperature properties and reducing changes in properties due to temperature. Another disadvantage of polyurethane rubber is its poor water resistance. For urethane rubber based on polyethylene adipate ester, it has been observed that hydrolysis has progressed in cleaning blades that have been manufactured for 2 to 4 years, although this varies depending on the usage conditions. Ru. This is mainly due to the molecular cleavage of ester bonds, which progresses gradually at first, but once it has progressed to a certain extent, the organic acid produced by hydrolysis acts as an accelerator, leading to rapid deterioration. Those that have undergone advanced hydrolysis become soft in the summer and lack firmness, making it impossible to obtain a sufficient cleaning effect, and in the winter, the elasticity decreases due to crystallization, resulting in insufficient cleaning. In order to compare hydrolysis resistance, a small amount of water was placed at the bottom of a sealed container, the sample was hung above it so as not to come into direct contact with the water, and the sample was kept at 70℃ for 35 days.The physical properties obtained were as follows: The changes in are shown in the table below.
【表】
上表のように、1,6―ヘキサンジオールとネ
オペンチルグリコール9:1のものは、ポリエチ
レングリコールアジペートエステルをベースとす
るポリウレタンゴムに対し非常に耐加水分解性が
すぐれている。その理由は本発明による方がエス
テル結合濃度が低く、ネオペンチルグリコールの
メチル基による立体障害によるものと考えられ
る。
クリーニングブレードを製造するための加工方
法として、従来注入成形法が一般であり、120〜
140℃にて脱水処理したポリエステルにポリイソ
シアネートを反応させたプレポリマーに硬化剤を
加えて架橋反応することにより得られる。この際
ポリエステルの分子量1000以下であると硬化剤を
加えた架橋反応において反応速度が早すぎて注入
成形が完全に行なわれない欠点があり、ポリエス
テルの分子量4000以上であるとポリエステルの粘
度が高すぎて、又架橋反応が遅すぎて硬化が遅
く、又脱泡不充分でブレード面に泡欠け部を生じ
る欠点がある。
以上のように本発明によれば、物性の温度によ
る変化が小さく、耐久性のあるクリーニングブレ
ードを提供しうる。[Table] As shown in the above table, 1,6-hexanediol and neopentyl glycol in a ratio of 9:1 has much better hydrolysis resistance than polyurethane rubber based on polyethylene glycol adipate ester. The reason for this is thought to be that the concentration of ester bonds is lower in the present invention and steric hindrance is caused by the methyl group of neopentyl glycol. Conventionally, injection molding is a common processing method for manufacturing cleaning blades, and
It is obtained by adding a curing agent to a prepolymer made by reacting polyester with polyisocyanate that has been dehydrated at 140°C and carrying out a crosslinking reaction. In this case, if the molecular weight of the polyester is less than 1000, the reaction rate in the crosslinking reaction with the addition of a curing agent will be too fast and injection molding will not be completed completely, and if the molecular weight of the polyester is more than 4000, the viscosity of the polyester will be too high. In addition, the crosslinking reaction is too slow, resulting in slow curing, and the defoaming is insufficient, resulting in bubble defects on the blade surface. As described above, according to the present invention, it is possible to provide a durable cleaning blade whose physical properties change little due to temperature.
Claims (1)
リコールのモル比が9/1〜5/5のグリコールとアジ
ピン酸より成る平均分子量1000〜4000のポリエス
テルと、ポリイソシアネートとの反応生成物であ
るウレタンゴムからなる、感光体の表面を摺擦し
てクリーニングするに用いる電子写真複写機用ク
リーニングブレード。1 From urethane rubber, which is the reaction product of polyisocyanate and polyester with an average molecular weight of 1000 to 4000, consisting of glycol and adipic acid with a molar ratio of 1,6-hexanediol to neopentyl glycol of 9/1 to 5/5. A cleaning blade for electrophotographic copying machines used to rub and clean the surface of a photoreceptor.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP20240782A JPS5991473A (en) | 1982-11-18 | 1982-11-18 | Cleaning blade for electrophotographic copying machine |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP20240782A JPS5991473A (en) | 1982-11-18 | 1982-11-18 | Cleaning blade for electrophotographic copying machine |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5991473A JPS5991473A (en) | 1984-05-26 |
| JPH0126065B2 true JPH0126065B2 (en) | 1989-05-22 |
Family
ID=16456994
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP20240782A Granted JPS5991473A (en) | 1982-11-18 | 1982-11-18 | Cleaning blade for electrophotographic copying machine |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5991473A (en) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS61140976A (en) * | 1984-12-12 | 1986-06-28 | Bando Chem Ind Ltd | Cleaning blade of electrophotographic copying machine |
| JPS6261088A (en) * | 1985-09-11 | 1987-03-17 | Toyo Tire & Rubber Co Ltd | Cleaning blade for photosensitive body of electrophotographic copying machine |
| JPH0658586B2 (en) * | 1985-12-20 | 1994-08-03 | 横浜ゴム株式会社 | Cleaning member for electrophotographic copying machine |
| JPS638685A (en) * | 1986-06-30 | 1988-01-14 | Yokohama Rubber Co Ltd:The | Cleaning member for electrophotographic copying machine |
| DE69921012T2 (en) * | 1998-05-13 | 2006-02-02 | Canon K.K. | Cleaning method in an electrophotographic apparatus and electrophotographic method using this cleaning method |
| JP2005345634A (en) * | 2004-06-01 | 2005-12-15 | Toyo Tire & Rubber Co Ltd | Cleaning blade and manufacturing method thereof |
-
1982
- 1982-11-18 JP JP20240782A patent/JPS5991473A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5991473A (en) | 1984-05-26 |
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