JPS6030941B2 - Surface coating of contact metal parts of transport transfer paper in electrophotographic copying machines - Google Patents
Surface coating of contact metal parts of transport transfer paper in electrophotographic copying machinesInfo
- Publication number
- JPS6030941B2 JPS6030941B2 JP56031203A JP3120381A JPS6030941B2 JP S6030941 B2 JPS6030941 B2 JP S6030941B2 JP 56031203 A JP56031203 A JP 56031203A JP 3120381 A JP3120381 A JP 3120381A JP S6030941 B2 JPS6030941 B2 JP S6030941B2
- Authority
- JP
- Japan
- Prior art keywords
- transfer paper
- tin oxide
- amount
- coating
- 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.)
- Expired
Links
- 238000000576 coating method Methods 0.000 title claims description 28
- 238000012546 transfer Methods 0.000 title claims description 26
- 239000011248 coating agent Substances 0.000 title claims description 24
- 229910052751 metal Inorganic materials 0.000 title claims description 11
- 239000002184 metal Substances 0.000 title claims description 11
- 239000011347 resin Substances 0.000 claims description 28
- 229920005989 resin Polymers 0.000 claims description 28
- 239000000843 powder Substances 0.000 claims description 23
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 claims description 20
- 229910001887 tin oxide Inorganic materials 0.000 claims description 20
- 239000000126 substance Substances 0.000 claims description 13
- 229910052731 fluorine Inorganic materials 0.000 claims description 4
- 239000011737 fluorine Substances 0.000 claims description 4
- 239000000203 mixture Substances 0.000 claims description 3
- 125000001153 fluoro group Chemical group F* 0.000 claims 1
- 239000000654 additive Substances 0.000 description 12
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 11
- 238000005299 abrasion Methods 0.000 description 9
- 230000000996 additive effect Effects 0.000 description 8
- 239000002245 particle Substances 0.000 description 8
- 238000012360 testing method Methods 0.000 description 8
- 230000005611 electricity Effects 0.000 description 7
- 238000000034 method Methods 0.000 description 7
- 230000003068 static effect Effects 0.000 description 7
- 239000000835 fiber Substances 0.000 description 6
- 229910002804 graphite Inorganic materials 0.000 description 6
- 239000010439 graphite Substances 0.000 description 6
- 239000004810 polytetrafluoroethylene Substances 0.000 description 6
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 6
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 5
- -1 and for this purpose Substances 0.000 description 5
- XMVONEAAOPAGAO-UHFFFAOYSA-N sodium tungstate Chemical compound [Na+].[Na+].[O-][W]([O-])(=O)=O XMVONEAAOPAGAO-UHFFFAOYSA-N 0.000 description 5
- 229920000742 Cotton Polymers 0.000 description 4
- 229910052782 aluminium Inorganic materials 0.000 description 4
- 239000004744 fabric Substances 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 3
- 239000003973 paint Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 238000010304 firing Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 235000015393 sodium molybdate Nutrition 0.000 description 2
- 239000011684 sodium molybdate Substances 0.000 description 2
- TVXXNOYZHKPKGW-UHFFFAOYSA-N sodium molybdate (anhydrous) Chemical compound [Na+].[Na+].[O-][Mo]([O-])(=O)=O TVXXNOYZHKPKGW-UHFFFAOYSA-N 0.000 description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 2
- 239000010935 stainless steel Substances 0.000 description 2
- QNRATNLHPGXHMA-XZHTYLCXSA-N (r)-(6-ethoxyquinolin-4-yl)-[(2s,4s,5r)-5-ethyl-1-azabicyclo[2.2.2]octan-2-yl]methanol;hydrochloride Chemical compound Cl.C([C@H]([C@H](C1)CC)C2)CN1[C@@H]2[C@H](O)C1=CC=NC2=CC=C(OCC)C=C21 QNRATNLHPGXHMA-XZHTYLCXSA-N 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000003868 ammonium compounds Chemical class 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 229910002090 carbon oxide Inorganic materials 0.000 description 1
- 210000000078 claw Anatomy 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229940072033 potash Drugs 0.000 description 1
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 1
- 235000015320 potassium carbonate Nutrition 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 1
- TXEYQDLBPFQVAA-UHFFFAOYSA-N tetrafluoromethane Chemical compound FC(F)(F)F TXEYQDLBPFQVAA-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G15/00—Apparatus for electrographic processes using a charge pattern
- G03G15/20—Apparatus for electrographic processes using a charge pattern for fixing, e.g. by using heat
- G03G15/2003—Apparatus for electrographic processes using a charge pattern for fixing, e.g. by using heat using heat
- G03G15/2014—Apparatus for electrographic processes using a charge pattern for fixing, e.g. by using heat using heat using contact heat
- G03G15/2053—Structural details of heat elements, e.g. structure of roller or belt, eddy current, induction heating
- G03G15/2057—Structural details of heat elements, e.g. structure of roller or belt, eddy current, induction heating relating to the chemical composition of the heat element and layers thereof
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G15/00—Apparatus for electrographic processes using a charge pattern
- G03G15/20—Apparatus for electrographic processes using a charge pattern for fixing, e.g. by using heat
- G03G15/2003—Apparatus for electrographic processes using a charge pattern for fixing, e.g. by using heat using heat
- G03G15/2014—Apparatus for electrographic processes using a charge pattern for fixing, e.g. by using heat using heat using contact heat
- G03G15/2017—Structural details of the fixing unit in general, e.g. cooling means, heat shielding means
- G03G15/2028—Structural details of the fixing unit in general, e.g. cooling means, heat shielding means with means for handling the copy material in the fixing nip, e.g. introduction guides, stripping means
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Paper Feeding For Electrophotography (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Paints Or Removers (AREA)
Description
【発明の詳細な説明】
本発明は電子写真複写機における搬送転写紙の接触金属
部品の表面被膜に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a surface coating of contact metal parts of a transport transfer paper in an electrophotographic copying machine.
一般に電子写真複写機の金属部品、特に加熱ローフー、
転写紙送り爪および搬送転写紙(以下転写紙という)の
滑り性を良好ならしめるための金属板(スライド板)等
は、電子写真複写機の実用時に高温下(130〜240
00程度)に保持されることから、それら部品の表面は
、用途により一様ではないが、少なくとも耐熱性で非粘
着性、滑り性、通電性(静電気防止性)および耐摩耗性
等の1つまたは2つ以上の性質を併有することが要求さ
れている。Metal parts of electrophotographic copiers in general, especially heating low-fu,
The metal plate (slide plate), etc. used to improve the slipperiness of the transfer paper feeding claw and conveyance transfer paper (hereinafter referred to as transfer paper) is heated under high temperatures (130 to 240℃) during the practical use of electrophotographic copying machines.
00), the surfaces of these parts vary depending on the application, but at least have one of the following properties: heat resistance, non-adhesiveness, slipperiness, electrical conductivity (antistatic properties), and abrasion resistance. Or, it is required to have two or more properties at the same time.
特に近時電子写真複写機における複写性能の高速化に伴
い、前記複写機の金属部品等は搬送転写紙との摩擦によ
る帯電が避けられないばかりでなく、高温下における被
膜の摩耗や摩損等の諸問題の解決方が重要な課題となっ
て釆た。非粘着性はトナーの熱融着物の付着防止の上か
ら必要なことで、このためには非粘着性にすぐれている
ふつ素樹脂が最適の被膜材料として一般的に用いられ、
しかもふつ素樹脂のうち250qo附近の温度まで安定
して使用できる四ふつ化エチレン樹脂(以下PTFEと
いう)およびパーフロロアルコキシ四ふつ化エチレン樹
脂(以下PFAという)が使用される。しかしながらこ
れら樹脂による被膜は、前記高温に耐えることができる
が、該高温時における摩耗が比較的多く、その上通電性
がないために、僅かの表面摩擦によっても帯電するとい
う欠点がある。In particular, with the recent increase in the speed of copying performance in electrophotographic copying machines, the metal parts of the copying machines are not only unavoidably charged due to friction with the conveying transfer paper, but also suffer from wear and abrasion of the coating under high temperatures. How to solve various problems became an important issue. Non-adhesiveness is necessary to prevent the adhesion of toner heat-fused substances, and for this purpose, fluorine resins, which have excellent non-adhesive properties, are generally used as the optimal coating material.
Furthermore, among the fluorine resins, tetrafluoroethylene resin (hereinafter referred to as PTFE) and perfluoroalkoxytetrafluoroethylene resin (hereinafter referred to as PFA), which can be stably used up to temperatures around 250 qo, are used. However, although coatings made of these resins can withstand the above-mentioned high temperatures, they suffer from relatively high abrasion at the high temperatures and, furthermore, have the disadvantage that they are not electrically conductive and therefore become charged even by slight surface friction.
このためPTFEまたはPFA樹脂被膜を形成した前記
加熱ローラ、転写紙送り爪、スライド板等は転写紙との
滑り性はこれら樹脂以外の樹脂被膜と比べてすぐれては
いても、転写紙との接触滑りでその被膜面に帯電し、こ
のため該面に転写紙が巻きついたり、あるいはこれが部
品間に語ったりし易いという欠点のあることが指摘され
ている。か)る見地からこの種ふつ素樹脂の通電性と耐
摩耗性に起因した前記の欠点を解決するため、従釆から
各種の考案がなされ、例えばふつ素樹脂(PTFE,P
FA)の改質を意図して該樹脂に、アルミニウム粉末、
銅粉末、ステンレス粉末、カーボンブラック、グラフア
イト粉末およびポロンナィトラィド粉末等の1または2
種以上を添加する方法、さらにはモリブデン酸化合物を
添加する方法等が公知である(以下上記物質を総称して
添加物という)。しかしながら上記公知の方法における
前記添加物の使用は、本発明者等の実験によればその添
加量がふつ素樹脂に対してある所定量を逸脱して過量と
なると、該樹脂の非粘着性が低下するばかりでなく、被
膜強度が低下して金属部品に対する付着強度の低下を招
来する。For this reason, even though the heating roller, transfer paper feed pawl, slide plate, etc. coated with a PTFE or PFA resin coating has superior sliding properties with the transfer paper compared to resin coatings other than these resins, contact with the transfer paper may be difficult. It has been pointed out that there is a drawback in that the coated surface is charged due to slippage, and the transfer paper is therefore likely to wrap around the surface, or that this tends to spread between parts. In order to solve the above-mentioned drawbacks caused by the electrical conductivity and abrasion resistance of this type of fluororesin, various ideas have been made from the viewpoint of fluororesin (PTFE, P
Aluminum powder,
1 or 2 of copper powder, stainless steel powder, carbon black, graphite powder, polonitride powder, etc.
A method of adding a species or more, and a method of adding a molybdic acid compound, etc. are known (hereinafter, the above substances are collectively referred to as additives). However, according to experiments conducted by the present inventors, when the additive is used in the known method, if the amount added deviates from a predetermined amount relative to the fluororesin and becomes excessive, the non-adhesive property of the resin deteriorates. Not only this, but also the coating strength decreases, leading to a decrease in the adhesion strength to metal parts.
このためか)る添加物の対樹脂添加量は、該添加物の種
類、粒径および比重等によって決める必要があるが、ふ
つ素適脂の場合重量比で約15%が限度である。従って
ふつ素樹脂に前記添加物中の金属粉末やグラフアィト粉
末を添加して所望する通電性を得るには、前記粉末を樹
脂に対し、相当に増量する必要があり、特に対象樹脂力
ミPTFE分散液であると、該分散液中のSTFEの粒
径が約0.1ムである関係上、添加物粉末の粒径もほべ
同等であることが必要となるが、か)る粒径の添加粉末
を得ることは実質的に困難であるため実用性に欠ける。For this reason, the amount of the additive to be added to the resin must be determined depending on the type, particle size, specific gravity, etc. of the additive, but in the case of fluorine-containing fat, the weight ratio is about 15% at most. Therefore, in order to obtain the desired electrical conductivity by adding metal powder or graphite powder among the additives to a fluororesin, it is necessary to increase the amount of the powder considerably relative to the resin. If it is a liquid, the particle size of STFE in the dispersion is about 0.1 mm, so the particle size of the additive powder needs to be about the same. Since it is substantially difficult to obtain the additive powder, it is impractical.
またこの添加物がモリブデン酸化合物例えばソーダ化合
物、アンモニウム化合物またはカリ化合物のいずれであ
っても、それらは水溶性であるため、か)る化合物を樹
脂被膜中に多量に含有せしめることは、得られる被膜の
安定性を阻害して好ましくない。このことは例えばモリ
ブデン酸ソーダを対PTFEII.紅重量%添加した塗
液を所望金属表面に塗布、焼成後水洗すると、この被膜
表面は変色して実用性に欠けることからも自明である。
従って得られる樹脂被膜の通電性については、次の手法
によってこれを確認した。すなわち通電性の良否は計器
によって測定することができるが、測定日時や測定条件
により甚だ不安定であるために、供試片(アルミニウム
板100側×200肋×3側)の表面に予め前記添加物
被膜を形成した後、該被膜面を白木綿布で20回こすり
、該表面に15肋中の短冊状に切断した白紙(未使用の
転写機)をのせ、その上面から指で軽く短冊紙を押えて
この紙を手前に引くことによって静電気による転写紙の
付着の有無を観察することにより確認した。その結果従
来から有効であるとされた前記添加物すなわちアルミニ
ウム、銅、ステンレスの各粉末、無機物質粉末およびそ
の化合物等の如きは、対樹脂少なくとも約15重量%含
有せしめない限り摩擦による帯電の起こることが認めら
れた。そこで本発明者等は前記添加物についてさらに研
究した結果、その添加量が対樹脂15重量%未満であっ
て、従来良好な通電性を有するとして公知な酸化錫微粉
末(粒径0.1ム)を混用することによって、高温下に
おける耐摩耗性の極めてすぐれていることを実験的に見
出し、しかもその単用のみならずこれと他の通電性物質
例えばタングステン酸ソーダまたはグラフアィト繊維粉
末の適量を混用(たゞし酸化錫添加量15重量%未満)
することにより得られる被膜に所望する通電性と耐摩耗
性とを同時に具備せしめ得ることに成功したものである
。以下かくして得られた樹脂被膜と関連被膜の通電性お
よび耐摩耗性(摩耗量表示)について実施した試験の一
例を第1表および第2表に示す。Furthermore, regardless of whether this additive is a molybdic acid compound such as a soda compound, an ammonium compound, or a potash compound, since they are water-soluble, it is possible to contain a large amount of such compound in the resin coating. This is undesirable because it impairs the stability of the coating. This applies, for example, to sodium molybdate versus PTFEII. It is obvious that if a coating liquid containing % red by weight is applied to a desired metal surface and washed with water after firing, the surface of the coating will change color and be impractical.
Therefore, the electrical conductivity of the resin coating obtained was confirmed by the following method. In other words, the conductivity can be measured with a meter, but since it is extremely unstable depending on the measurement date and time and measurement conditions, the above-mentioned additives are added to the surface of the test piece (aluminum plate 100 side x 200 ribs x 3 sides) in advance. After forming a material film, rub the surface of the film 20 times with a white cotton cloth, place a piece of white paper (unused transfer machine) cut into 15 square strips on the surface, and lightly roll the strip of paper from the top surface with your fingers. By holding the paper and pulling it towards you, it was confirmed whether or not the transfer paper was stuck due to static electricity. As a result, the additives that have been considered effective in the past, such as powders of aluminum, copper, and stainless steel, powders of inorganic substances, and their compounds, are charged by friction unless they are contained at least about 15% by weight relative to the resin. This was recognized. As a result of further research on the additive, the present inventors found that the amount added was less than 15% by weight based on the resin, and that fine tin oxide powder (particle size 0.1 μm), which is conventionally known to have good electrical conductivity, was used. ) has been experimentally found to have extremely excellent abrasion resistance under high temperatures.In addition to its single use, it has also been found that by mixing it with an appropriate amount of other electrically conductive substances such as sodium tungstate or graphite fiber powder. Mixed use (added amount of tin oxide less than 15% by weight)
By doing so, the resulting film was successfully provided with desired electrical conductivity and abrasion resistance at the same time. Tables 1 and 2 show examples of tests conducted on the electrical conductivity and abrasion resistance (display of wear amount) of the thus obtained resin coatings and related coatings.
第1表(付 記)
本表は供試片(アルミニウム板low岬×20仇奴×3
肋)の13000における転写紙による摩耗量および静
電気の発生状態を示したもので、川 摩耗量は荷重51
g/地の下に150肌/回走行、2回走行/秒の条件で
100,000回実施後における平均測定値である‘o
’静電気による転写紙付着の有無は、供謎片を白木綿布
で20回こすり、該面に15肋中の短冊状に切断した未
使用の転写紙をのせ、その表面を軽く指圧して転写紙が
供謎片に付着するや否やを確認し、その有無を判断した
。Table 1 (Appendix) This table shows the test pieces (aluminum plate low cape x 20 enemies x 3
This figure shows the amount of wear caused by the transfer paper and the generation of static electricity at 13,000 (load).
'o is the average measured value after 100,000 runs under the conditions of 150 skins/running under the ground and 2 running/seconds.
'To check whether the transfer paper has adhered due to static electricity, rub the donor piece with a white cotton cloth 20 times, place an unused transfer paper cut into 15 strips on the surface, and gently press the surface of the transfer paper with your fingertips. The presence or absence of the substance was determined by checking as soon as it adhered to the offering piece.
し一 良否は添加物の対樹脂添加量(15重量%未満)
、摩耗量および静電気による転写紙付着の3者総合判定
結果を示し、◎:最良、0:良、×:不良(不適)を示
す。Shiichi: Quality is determined by the amount of additive added to the resin (less than 15% by weight)
, shows the three-way comprehensive judgment results of the amount of wear and adhesion of transfer paper due to static electricity, ◎: best, 0: good, ×: poor (unsuitable).
第2表
(付 記)
本表は供教片(第1表付記に同じ)の180℃における
転写紙による摩耗量および静電気の発生状態を示したも
ので、【ィー 摩耗量,{o’静電気による転写紙付着
の有無およびし一良否については第1表付記々戦の方法
によつた。Table 2 (Appendix) This table shows the amount of wear caused by the transfer paper and the generation of static electricity on the test piece (same as the note in Table 1) at 180°C. The presence or absence of adhesion of the transfer paper due to static electricity and its quality were determined according to the method described in Table 1.
上記第1,第2表から明らかなように、樹脂の種類と適
用温度によって摩耗量は異るが通電性(静電気防止性)
および耐摩耗性(摩耗量表示)は、添加物に酸化錫(単
体)を対樹脂(PTFE,PFA)15重量%未満すな
わち1箱重量%混用した場合の被膜が最適(第1表M.
2、第2表地.2参照)で、静電気による転写紙付着も
なく、また摩耗量も20.7〜26.5の9と少なく、
最良であることが判る。As is clear from Tables 1 and 2 above, the amount of wear varies depending on the type of resin and the applied temperature, but the electrical conductivity (antistatic property)
In terms of wear resistance (display of wear amount), a coating containing less than 15% by weight of tin oxide (single substance) relative to the resin (PTFE, PFA), that is, 1% by weight of the box, is optimal (Table 1 M.
2. Second outer material. 2), there is no transfer paper adhesion due to static electricity, and the amount of wear is as low as 20.7 to 26.5 (9).
It turns out to be the best.
酸化錫(単体)に続いて前記同様の添加条件下で、タン
グステン酸ソーダの単体およびこれと酸化錫との混合被
膜が通電性、耐摩耗性ともに良好(第1菱則o.3,N
o.4参照)ではあるが、前者(タングステン酸ソーダ
単体)は対樹脂添加量が16.5重量%となり、水溶性
物質を多く塗膜内に含有するので不利である。これに反
して後者は酸化錫の混用によって所望する良結果の得ら
れることが知られる。またモリブデン酸ソーダはタング
ステン酸ソーダと混用して良好な通電性は得られ(第1
表船.5,No.6参照)ても、被膜の摩耗量が特に後
者が多く、対酸化錫単体およびこれとタングステン酸ソ
ーダ混用の2倍以上にも相当し、実用性に欠ける。Following tin oxide (single substance), under the same addition conditions as above, sodium tungstate alone and a mixed film of this and tin oxide had good electrical conductivity and wear resistance (first rhombic rule o.3, N
o. However, the former (sodium tungstate alone) is disadvantageous because the amount added to the resin is 16.5% by weight, and a large amount of water-soluble substances is contained in the coating film. On the other hand, it is known that the desired results can be obtained with the latter by mixing tin oxide. In addition, good electrical conductivity can be obtained by mixing sodium molybdate with sodium tungstate (first
Front ship. 5, No. However, the wear amount of the coating is particularly large in the latter case, and is more than twice as much as that of tin oxide alone or a mixture of tin oxide and sodium tungstate, which is impractical.
さらにまたグラフアィト繊維微粉末(単体)使用のもの
(第2表No.5参照)は、対樹脂添加量13重量%に
おいて通電性は良好であるとしても、摩耗量が78の9
と対酸化錫約3倍にも達して不適である。Furthermore, in the case of using graphite fiber fine powder (single substance) (see Table 2 No. 5), although the electrical conductivity was good at 13% by weight of the resin, the amount of wear was 78%.
This amount is about three times as high as that of tin oxide, making it unsuitable.
しかしグラフアィト繊維微粉末、ふ化炭素および酸化錫
3者混用のもの(第2表船.8参照)は、対樹脂1$重
量%と前記グラファィト繊維微粉末(単体)と同量比で
あるに拘わらず、通電性は良好で摩耗量も35.3雌と
グラフアイト繊維微粉末使用時の約1/2以下の量で良
好であることが判る。このように樹脂被膜の通電性およ
び耐摩耗性を良好ならしめて所望効果を得るには、酸化
錫(単体)を対樹脂15重量%以下混合することが最適
である。However, the mixture of graphite fiber fine powder, hatched carbon, and tin oxide (refer to Table 2.8) has a ratio of 1% by weight to the resin, which is the same amount as the graphite fiber fine powder (single substance). First, it can be seen that the conductivity is good and the amount of wear is 35.3 mm, which is about 1/2 or less when using fine graphite fiber powder. In order to improve the conductivity and abrasion resistance of the resin coating and obtain the desired effect, it is optimal to mix 15% by weight or less of tin oxide (single substance) with respect to the resin.
しかして上記において酸化錫(単体)の対樹脂混合比が
16重量%となると、通電性は良くとも表面組度が大き
くなるために摩耗量が130〜179の9となり、しか
も道用々紙(転写紙)のいたみが特に甚だしく到底実用
に耐えないものとなる。However, when the mixing ratio of tin oxide (single substance) to the resin is 16% by weight, the electrical conductivity is good, but the degree of surface assembly becomes large, so the amount of wear is 130 to 179 (9). The damage to the transfer paper (transfer paper) is particularly severe, making it completely unusable.
このことはさきに述べた被膜物性の劣化によるものと思
料され、この点からも酸化錫添加量は対樹脂15重量%
未満であることが望ましい。This is thought to be due to the deterioration of the physical properties of the film mentioned earlier, and from this point of view, the amount of tin oxide added was 15% by weight based on the resin.
It is desirable that it be less than
以下実施例によって本発明をさらに具体的に説明する。
実施例 1
アルミニウム板(10仇肋×20仇肋×3側)を供試片
としてその表面に常法によりブラスト加工を施した後、
該面にPTFE塗料のプラィマーに酸化錫微粉末粒径0
.1山(三菱金属■製:T−1)500gを水500g
とロールねりし、これを対PTFEIO%となる如く鷹
洋混合して得た塗料を塗膜厚さが約7Aとなる如く塗布
後330午0の下で10分間焼成する。The present invention will be explained in more detail below with reference to Examples.
Example 1 An aluminum plate (10 ribs x 20 ribs x 3 sides) was used as a test piece, and its surface was blasted using a conventional method.
Tin oxide fine powder particle size 0 is applied to the PTFE paint primer on the surface.
.. 1 pile (Mitsubishi Metal ■: T-1) 500g and water 500g
The resulting paint was mixed with Takayo at a ratio of PTFEIO% to a coating thickness of about 7A, and then baked at 330°C for 10 minutes.
次いでその上面に、PTFEの上塗々料に同様にして酸
化錫微粉末(粒径0.1り)を対塗料樹脂比1箱重量%
の割に混合して得た塗料を、その塗膜厚さが28仏とな
る如く塗布後40000の高温下に10分間焼成し、厚
さ35仏の被膜を得た。この被膜は第1表付記々載の方
法によって耐摩耗試験を行なったが、その結果は20.
7の9/100,000回(13000で)として得ら
れ、さらに白木綿布でその表面を20回こすったが、該
面に転写紙の付着は全く見られず満足すべきものであっ
た。Then, on the top surface of the PTFE top coat, fine tin oxide powder (particle size 0.1) was applied in an amount of 1% by weight of the paint resin.
After coating, the resulting coating material was baked at a high temperature of 40,000 mm for 10 minutes to obtain a film with a thickness of 35 mm. This coating was subjected to an abrasion resistance test according to the method listed in Table 1, and the results were 20.
The surface was rubbed 20 times with a white cotton cloth, but no transfer paper was observed on the surface, which was satisfactory.
実施例 2実施例1と同様の供試片を予めアルカリ脱脂
後塩酸(15%)でエッチングし水洗後乾燥する。Example 2 A test piece similar to Example 1 was previously degreased with alkali, etched with hydrochloric acid (15%), washed with water, and then dried.
次いでPFA粉末に対し酸化錫微粉末(粒径0.1仏)
の9.1重量%を加え、ボールミルにより3時間縄拝混
合した粉末を静電粉体塗装法によって前記処理後の供試
片に塗膜厚さが50仏となる如く塗布し42000で1
5分間焼成して50山の被膜を得た。このものは第2表
付記々教の方法によって摩耗量を測定したところ、40
〜42の9/100,000回の良結果を示したのに対
し、白木綿布で該面をこすった結果は、わずかに転写紙
の付着が見られる程度(帯電)であって、完全通電を必
要としない部品類への適用が可能であった。実施例 3
実施例1と同様の供試片に実施例1と同様にプラィマー
を厚さ7仏に塗布した。Next, tin oxide fine powder (particle size 0.1 French) was added to the PFA powder.
9.1 wt.
After firing for 5 minutes, a film with 50 peaks was obtained. When the amount of wear of this item was measured using the method described in Table 2, it was found to be 40.
~42 showed a good result of 9/100,000 times, whereas the result of rubbing the surface with a white cotton cloth showed that there was only a slight adhesion of transfer paper (electrification), and it was not possible to fully energize. It was possible to apply it to unnecessary parts. Example 3 A primer similar to Example 1 was applied to a test piece similar to Example 1 to a thickness of 7 mm.
次いでPFA粉末にグラフアィト繊維微粉末(粒径10
仏)(日本カーボン■製)を対PFA8.G重量%、酸
化錫2.6重量%およびふつ化炭素(日本カーボン■製
)1.7重量%をそれぞれ加え、ボールミルにより5時
間損拝混合して上塗々料を得、該塗料を前記プラィマー
の表面に実施例2と同機に静電粉体塗装を行ない。38
0qoの高温下に30分間焼成して厚さ90〜100ム
の塗膜を得た。Next, graphite fiber fine powder (particle size 10
(France) (manufactured by Nippon Carbon ■) to PFA8. % by weight of G, 2.6% by weight of tin oxide, and 1.7% by weight of carbon fluoride (manufactured by Nippon Carbon ■) were added and mixed in a ball mill for 5 hours to obtain a top coat. Electrostatic powder coating was applied to the surface of the same machine as in Example 2. 38
The coating was baked at a high temperature of 0 qo for 30 minutes to obtain a coating film with a thickness of 90 to 100 mm.
Claims (1)
粉末および他の通電性物質との混合物からなり、前記酸
化錫微粉末が対ふつ素樹脂15重量%未満含有した被膜
を電子写真複写機中搬送される転写紙の接触金属部品の
表面に形成したことを特徴とする電子写真複写機におけ
る搬送転写紙の接触金属部品の表面被膜。1. Electrophotographic copying of a coating consisting of a fluororesin and a fine tin oxide powder alone or a mixture of the fine tin oxide powder and another electrically conductive substance, and containing less than 15% by weight of the fine tin oxide powder relative to the fluorine resin. A surface coating of a contact metal part of a conveyed transfer paper in an electrophotographic copying machine, characterized in that it is formed on the surface of a contact metal part of a transfer paper conveyed in the machine.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP56031203A JPS6030941B2 (en) | 1981-03-06 | 1981-03-06 | Surface coating of contact metal parts of transport transfer paper in electrophotographic copying machines |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP56031203A JPS6030941B2 (en) | 1981-03-06 | 1981-03-06 | Surface coating of contact metal parts of transport transfer paper in electrophotographic copying machines |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS57146264A JPS57146264A (en) | 1982-09-09 |
| JPS6030941B2 true JPS6030941B2 (en) | 1985-07-19 |
Family
ID=12324852
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP56031203A Expired JPS6030941B2 (en) | 1981-03-06 | 1981-03-06 | Surface coating of contact metal parts of transport transfer paper in electrophotographic copying machines |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6030941B2 (en) |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6080883A (en) * | 1983-10-11 | 1985-05-08 | Fuji Xerox Co Ltd | Heat fixing roll |
| JPS60162275A (en) * | 1984-02-03 | 1985-08-24 | Fuji Xerox Co Ltd | Form peeling device of image forming device |
| JPS61203154A (en) * | 1985-02-04 | 1986-09-09 | Daikin Ind Ltd | Antistatic fluororesin composition |
| JPS61277985A (en) * | 1985-05-31 | 1986-12-08 | Canon Inc | Separation device with separation claws |
| JPH0827572B2 (en) * | 1986-05-30 | 1996-03-21 | ミノルタ株式会社 | Heat roller fixing device |
| JPH01187582A (en) * | 1988-01-22 | 1989-07-26 | Canon Inc | Fusing device |
| JPH0786726B2 (en) * | 1987-09-02 | 1995-09-20 | デュポン株式会社 | Separation claw for copier |
| JP2646218B2 (en) * | 1987-12-18 | 1997-08-27 | キヤノン株式会社 | Pressure roller for fuser |
| JPH05249862A (en) * | 1992-09-28 | 1993-09-28 | Fuji Xerox Co Ltd | Fixing roll in electrophotographic copying machine |
| US5464698A (en) * | 1994-06-29 | 1995-11-07 | Eastman Kodak Company | Fuser members overcoated with fluorocarbon elastomer containing tin oxide |
| JP2821414B2 (en) * | 1996-03-18 | 1998-11-05 | キヤノン株式会社 | Fixing device |
| JP4653452B2 (en) * | 2003-10-24 | 2011-03-16 | 株式会社リコー | Fixing member, fixing device, and image forming apparatus |
-
1981
- 1981-03-06 JP JP56031203A patent/JPS6030941B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS57146264A (en) | 1982-09-09 |
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