JPH02247678A - Separation pawl for copying machine - Google Patents
Separation pawl for copying machineInfo
- Publication number
- JPH02247678A JPH02247678A JP6814989A JP6814989A JPH02247678A JP H02247678 A JPH02247678 A JP H02247678A JP 6814989 A JP6814989 A JP 6814989A JP 6814989 A JP6814989 A JP 6814989A JP H02247678 A JPH02247678 A JP H02247678A
- Authority
- JP
- Japan
- Prior art keywords
- polyphenylene sulfide
- resin
- heat
- curvature
- sulfide 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.)
- Granted
Links
- 238000000926 separation method Methods 0.000 title description 33
- 229920005989 resin Polymers 0.000 claims abstract description 58
- 239000011347 resin Substances 0.000 claims abstract description 58
- 239000000835 fiber Substances 0.000 claims abstract description 39
- 239000004734 Polyphenylene sulfide Substances 0.000 claims abstract description 32
- 229920000069 polyphenylene sulfide Polymers 0.000 claims abstract description 32
- 229920002492 poly(sulfone) Polymers 0.000 claims abstract description 20
- 239000012210 heat-resistant fiber Substances 0.000 claims abstract description 13
- 210000000078 claw Anatomy 0.000 claims description 35
- 239000011342 resin composition Substances 0.000 claims description 3
- 239000000203 mixture Substances 0.000 abstract description 7
- 230000000694 effects Effects 0.000 abstract description 6
- 230000002411 adverse Effects 0.000 abstract description 3
- 230000000052 comparative effect Effects 0.000 description 13
- 239000003365 glass fiber Substances 0.000 description 11
- 238000000034 method Methods 0.000 description 11
- 238000005452 bending Methods 0.000 description 10
- 230000009477 glass transition Effects 0.000 description 9
- 239000000155 melt Substances 0.000 description 8
- 238000012360 testing method Methods 0.000 description 8
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 7
- 239000000945 filler Substances 0.000 description 7
- 230000003746 surface roughness Effects 0.000 description 7
- 239000012744 reinforcing agent Substances 0.000 description 6
- 239000004962 Polyamide-imide Substances 0.000 description 5
- 239000004695 Polyether sulfone Substances 0.000 description 5
- 230000008859 change Effects 0.000 description 5
- 230000007423 decrease Effects 0.000 description 5
- NJLLQSBAHIKGKF-UHFFFAOYSA-N dipotassium dioxido(oxo)titanium Chemical compound [K+].[K+].[O-][Ti]([O-])=O NJLLQSBAHIKGKF-UHFFFAOYSA-N 0.000 description 5
- 230000013011 mating Effects 0.000 description 5
- 238000000465 moulding Methods 0.000 description 5
- 229920002312 polyamide-imide Polymers 0.000 description 5
- 229920006393 polyether sulfone Polymers 0.000 description 5
- 239000002994 raw material Substances 0.000 description 5
- 229920000049 Carbon (fiber) Polymers 0.000 description 4
- 239000004917 carbon fiber Substances 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 3
- 230000001070 adhesive effect Effects 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 238000006482 condensation reaction Methods 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- 238000011049 filling Methods 0.000 description 3
- 239000010439 graphite Substances 0.000 description 3
- 229910002804 graphite Inorganic materials 0.000 description 3
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- FZHAPNGMFPVSLP-UHFFFAOYSA-N silanamine Chemical compound [SiH3]N FZHAPNGMFPVSLP-UHFFFAOYSA-N 0.000 description 3
- 239000000377 silicon dioxide Substances 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 239000000454 talc Substances 0.000 description 3
- 229910052623 talc Inorganic materials 0.000 description 3
- AJDIZQLSFPQPEY-UHFFFAOYSA-N 1,1,2-Trichlorotrifluoroethane Chemical compound FC(F)(Cl)C(F)(Cl)Cl AJDIZQLSFPQPEY-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 208000032544 Cicatrix Diseases 0.000 description 2
- 239000004697 Polyetherimide Substances 0.000 description 2
- 239000004642 Polyimide Substances 0.000 description 2
- 235000010724 Wisteria floribunda Nutrition 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 150000001491 aromatic compounds Chemical class 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 230000008878 coupling Effects 0.000 description 2
- 238000010168 coupling process Methods 0.000 description 2
- 238000005859 coupling reaction Methods 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 238000001746 injection moulding Methods 0.000 description 2
- 230000007774 longterm Effects 0.000 description 2
- 230000014759 maintenance of location Effects 0.000 description 2
- -1 methylol group Chemical group 0.000 description 2
- 239000010445 mica Substances 0.000 description 2
- 229910052618 mica group Inorganic materials 0.000 description 2
- 239000011490 mineral wool Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 239000008188 pellet Substances 0.000 description 2
- 229920001643 poly(ether ketone) Polymers 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 229920000570 polyether Polymers 0.000 description 2
- 229920001601 polyetherimide Polymers 0.000 description 2
- 229920001721 polyimide Polymers 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 230000003014 reinforcing effect Effects 0.000 description 2
- 231100000241 scar Toxicity 0.000 description 2
- 230000037387 scars Effects 0.000 description 2
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical class [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 2
- 229910010271 silicon carbide Inorganic materials 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 1
- HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 241000206761 Bacillariophyta Species 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- 235000010582 Pisum sativum Nutrition 0.000 description 1
- 240000004713 Pisum sativum Species 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 229920013632 Ryton Polymers 0.000 description 1
- 239000004736 Ryton® Substances 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
- 239000004963 Torlon Substances 0.000 description 1
- 229920003997 Torlon® Polymers 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 239000004760 aramid Substances 0.000 description 1
- 229920003235 aromatic polyamide Polymers 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 150000001879 copper Chemical class 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 229920006038 crystalline resin Polymers 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- PXJJSXABGXMUSU-UHFFFAOYSA-N disulfur dichloride Chemical compound ClSSCl PXJJSXABGXMUSU-UHFFFAOYSA-N 0.000 description 1
- 238000007580 dry-mixing Methods 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000011152 fibreglass Substances 0.000 description 1
- 239000010408 film Substances 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000010440 gypsum Substances 0.000 description 1
- 229910052602 gypsum Inorganic materials 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 229920006015 heat resistant resin Polymers 0.000 description 1
- 239000012760 heat stabilizer Substances 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 239000011968 lewis acid catalyst Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000006082 mold release agent Substances 0.000 description 1
- CWQXQMHSOZUFJS-UHFFFAOYSA-N molybdenum disulfide Chemical compound S=[Mo]=S CWQXQMHSOZUFJS-UHFFFAOYSA-N 0.000 description 1
- 229910052982 molybdenum disulfide Inorganic materials 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 238000005453 pelletization Methods 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 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
- 229920006254 polymer film Polymers 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- 230000002787 reinforcement Effects 0.000 description 1
- 229910052594 sapphire Inorganic materials 0.000 description 1
- 239000010980 sapphire Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 150000003457 sulfones Chemical class 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 125000000101 thioether group Chemical group 0.000 description 1
- 239000013008 thixotropic agent Substances 0.000 description 1
Abstract
Description
【発明の詳細な説明】 〔産業上の利用分野〕 この発明は、複写機用分離爪に関するものである。[Detailed description of the invention] [Industrial application field] The present invention relates to a separation claw for a copying machine.
従来の乾式複写機などの機器においては、文字または図
形等に対応して感光ドラムの表面に形成された静電荷潜
像をトナー像に変換した後、このトナー像を給紙カセッ
トから供給されて来る紙面に転写し、さらに転写された
トナー像を紙面に定着させるために加熱された定着ロー
ラによって表面を加熱加圧し、トナー像と紙繊維とを融
着させて両者が容易に離れないようにする機構が組み込
まれている。そして、定着ローラを通過した複写紙がロ
ーラに巻き付くことなく確実に排出されるために、分離
爪を用いてその先端をローラの外周面に密着させながら
複写機の端をすくい上げる方法が採られる。したがって
、このような分離爪においては、ローラの外周面に対し
て摩擦抵抗が小さく表面を損傷しないこと、充分な機械
的強度特に高温剛性を有し、その先端部形状に充分な精
度が得られること、さらにはトナーを粘着しないことな
どの特性が要求されてきた。In conventional devices such as dry copying machines, an electrostatic latent image formed on the surface of a photosensitive drum corresponding to characters or graphics is converted into a toner image, and then this toner image is supplied from a paper feed cassette. The toner image is then transferred to the paper surface, and in order to fix the transferred toner image on the paper surface, a heated fixing roller heats and presses the surface, fuses the toner image and paper fibers, and prevents them from separating easily. It has a built-in mechanism. In order to ensure that the copy paper that has passed through the fixing roller is ejected without getting wrapped around the roller, a method is adopted in which a separating claw is used to scoop up the edge of the copying machine while keeping its tip in close contact with the outer circumferential surface of the roller. . Therefore, such a separation claw has low frictional resistance against the outer circumferential surface of the roller so as not to damage the surface, has sufficient mechanical strength, especially high temperature rigidity, and has sufficient precision in the shape of its tip. In addition, properties such as non-adhesion of toner have been required.
そして、特に近年における需要動向においては、大企業
の事務所から中小企業の事務所、さらには一般家庭へと
広がっており、小型化、低価格化が切望されている。定
着部の各部品も同様に小型化、低価格化を前述したよう
な分離爪に不可欠な特性を失うことなく具備するように
期待されている。Especially in recent years, demand has expanded from offices of large companies to offices of small and medium-sized enterprises, and even to ordinary households, and there is a strong desire for smaller sizes and lower prices. It is expected that each part of the fixing unit will also be made smaller and lower in price without losing the characteristics essential to the separation claw as described above.
このような分離爪に不可欠な特性のうち、トナ−に対す
る非粘着性の改善については数多くの提案がなされてお
り、小型化、低価格化の要求にも対応できるものとして
、たとえば、フッ素化ポリエーテル重合体の被膜を分離
爪上に形成させる方法(特開昭61−236577号)
がある、この方法によれば低粘度の液体の中へ浸漬する
という安価な方法によって、小型化のために複雑化した
形状となったものでも容易に、しかも薄膜であることか
ら寸法、形状をくずさないで非粘着性被膜を施すことが
できる。Many proposals have been made to improve non-adhesiveness to toner, which is one of the essential characteristics of separation claws. Method of forming an ether polymer film on a separation nail (Japanese Patent Application Laid-Open No. 61-236577)
According to this method, by immersing it in a low-viscosity liquid, which is an inexpensive method, it is possible to easily change the size and shape of objects that have complicated shapes due to miniaturization, and because it is a thin film. A non-adhesive coating can be applied without breaking.
しかし、高温剛性、相手ロールの損傷性、爪先端部形状
の精度などについては、分離爪材に使用される耐熱性樹
脂または充填剤の種類によって大きく左右される0分離
爪材料としては、ポリイミド、ポリアミドイミド、ポリ
フェニレンサルファイド、ポリエーテルケトン、ポリエ
ーテルサルホン、ポリエーテルイミド、耐熱性芳族ポリ
エステル等が挙げられる。ポリイミド、ポリアミドイミ
ド、ポリエーテルケトンおよび耐熱性芳香族ポリエステ
ルは、補強剤なしか、または補強剤を併用することによ
って優れた高温剛性を発揮するが、高価であるため低価
格化の要求に応えきれず、また、ポリエーテルサルホン
、ポリエーテルイミド等の樹脂は、比較的安価であるが
、ガラス転移点が220°C前後でかつ非品性であるこ
とから、ガラス転移点以上の温度では軟化し、耐熱性が
低過ぎるため、定着ローラの加熱温度の低い、限定され
た複写機にしか使用できない。これは近年の複写機の高
速化に伴う定着温度の高温化ということからもより一層
限定された用途のみの使用となる。However, high-temperature rigidity, damage resistance to the mating roll, precision of the shape of the tip of the claw, etc. are largely affected by the type of heat-resistant resin or filler used in the separation claw material.As separation claw materials, polyimide, Examples include polyamideimide, polyphenylene sulfide, polyetherketone, polyethersulfone, polyetherimide, heat-resistant aromatic polyester, and the like. Polyimide, polyamideimide, polyetherketone, and heat-resistant aromatic polyester exhibit excellent high-temperature rigidity without or with a reinforcing agent, but they are expensive and cannot meet the demand for lower prices. Furthermore, although resins such as polyethersulfone and polyetherimide are relatively inexpensive, they have a glass transition point of around 220°C and are poor quality, so they soften at temperatures above the glass transition point. However, because its heat resistance is too low, it can only be used in limited copying machines where the heating temperature of the fixing roller is low. This method is used only for more limited applications because of the fact that the fixing temperature has become higher as the speed of copying machines has increased in recent years.
これらに対してポリフェニレンサルファイド樹脂は、安
価であり、溶融粘度も低いために小型化による薄肉また
は複雑化した部位にも容易に充填出来る特性を備えてい
るため、低価格化、小型化に対して非常に有利である。On the other hand, polyphenylene sulfide resin is inexpensive and has low melt viscosity, so it can be easily filled into thin walls or complicated areas due to miniaturization. Very advantageous.
また、ガラス転移点は90°C前後と低いが、結晶性樹
脂であるため、ガラス繊維、チタン酸カリウム繊維、炭
素繊維等の耐熱性繊維類、またはこれら繊維にマイカ、
タルク等の無機粉末充填剤を添加することに基づく補強
効果によって、耐熱性は大幅に向上する。しかし、補強
剤の充填量が多い場合は、相手ロールを傷つけるという
問題と、分散不良になりがちなため補強剤の爪先端部へ
の充填が不均一になり、耐熱性低下または先端部形状が
悪くなるという問題があり、逆に補強剤の充填量が少い
場合には、ポリフェニレンサルファイド樹脂の溶融粘度
が非常に小さいため、分離爪先端の滑らかな曲率半径が
得られず、時としてシャープなエツジ(パリ)になると
いう問題がある。また、補強剤の種類によっても、たと
えばチタン酸カリウム繊維などの短繊維を補強剤として
使用した分離爪は、曲げ強度、衝撃強度等の機械的強度
において劣り、高温時には剛性にも劣るという問題があ
り、ガラス繊維または炭素繊維では、補強効果に問題が
なくとも、分離爪を成形した時の表面粗さが大きく、先
端部の曲率半径も大きくなり過ぎ、良好な先端形状も得
られず、定着紙を円滑にすくい上げられなくなるばかり
か、分離方向が不良になるという現象も起こすことにな
る。Although the glass transition point is low at around 90°C, since it is a crystalline resin, heat-resistant fibers such as glass fiber, potassium titanate fiber, and carbon fiber, or mica,
The heat resistance is significantly improved by the reinforcing effect based on the addition of inorganic powder fillers such as talc. However, if the amount of reinforcing agent filled is large, there are problems such as damaging the mating roll and poor dispersion, which results in uneven filling of the reinforcing agent into the tip of the claw, resulting in a decrease in heat resistance or a change in the shape of the tip. On the other hand, if the amount of reinforcing agent filled is small, the melt viscosity of the polyphenylene sulfide resin is very low, so it is difficult to obtain a smooth radius of curvature at the tip of the separation claw, which sometimes results in a sharp curvature. There is the problem of becoming Etsuji (Paris). Furthermore, depending on the type of reinforcing agent, separation claws using short fibers such as potassium titanate fibers as reinforcing agents have problems in that they are inferior in mechanical strength such as bending strength and impact strength, and are also inferior in rigidity at high temperatures. With glass fiber or carbon fiber, even if there is no problem with the reinforcing effect, the surface roughness when forming the separation claw is large, the radius of curvature of the tip is too large, and a good tip shape cannot be obtained, making it difficult to fix. Not only will the paper not be scooped up smoothly, but the separation direction will also be incorrect.
(発明が解決しようとする課題〕
以上述べたように、従来の技術においては、高温剛性、
爪先端の衝撃強度または曲げ強度等の優れた機械的強度
のほかに爪先端部の好ましい曲率半径が容易に得られる
成形性、成形品の表面の平滑性等にも優れ、さらに低価
格でかつ小型化の要求に応じられる分離爪は得られてい
ないという問題点があり、これを解決することが課題で
あった。(Problem to be solved by the invention) As mentioned above, in the conventional technology, high temperature rigidity,
In addition to the excellent mechanical strength such as the impact strength or bending strength of the nail tip, it also has excellent moldability that allows the desired radius of curvature of the nail tip to be easily obtained, and the smoothness of the surface of the molded product. There is a problem in that a separation claw that meets the demand for miniaturization has not been obtained, and it has been a challenge to solve this problem.
上記の課題を解決するために、この発明はポリフェニレ
ンサルファイド樹脂100重量部、平均繊維径6μ以下
の耐熱性繊維20〜200重量部および耐熱性ポリスル
ホン樹脂10〜90重量部とを必須成分とするポリフェ
ニレンサルファイド樹脂組成物を用いた複写機用分離爪
とする手段を採用したものである。In order to solve the above problems, the present invention has developed a polyphenylene sulfide resin containing 100 parts by weight of polyphenylene sulfide resin, 20 to 200 parts by weight of heat-resistant fibers with an average fiber diameter of 6 μ or less, and 10 to 90 parts by weight of heat-resistant polysulfone resin. This method employs a separation claw for a copying machine using a sulfide resin composition.
以下その詳細を述べる。The details will be described below.
まず、この発明のポリフェニレンサルファイド樹脂はマ
トリックス用樹脂として使用されるものであり、低価格
にもかかわらず熱変形温度が260゛C以上と優れた耐
熱性を示し、溶融粘度が他の工ンジニアリングプラスチ
ックスと呼ばれる樹脂よりも低いため、複雑なまたは薄
肉の部位も容易に成形でき、またフィラー類の充填性が
優れていることから好ましい樹脂である。しかし、複写
機用分離爪として使用されるには、あまりにも溶融粘度
が低くて分離爪先端の滑らかな曲率半径が得られず、時
としてシャープなエツジ(パリ)になったりする、した
がって、溶融粘度が高いもの、具体的には300°Cで
の溶融粘度が6000ポイズ(オリフィス:直径1m、
長さ2鵬、荷重10kg)以上のものが好ましく、10
000ポイズのものが特に好ましい、そして、溶融粘度
の上限は溶融成形が可能な範囲で特に限定するものでは
ないが、経済的な見地から、射出成形で多数個取りを可
能にするために、50000ボイズ以下が好ましい。First, the polyphenylene sulfide resin of this invention is used as a matrix resin, and despite its low price, it exhibits excellent heat resistance with a heat distortion temperature of 260°C or higher, and a melt viscosity that is higher than that of other engineering resins. It is a preferable resin because it is lower than resins called plastics, so it can be easily molded into complex or thin parts, and it has excellent filling properties with fillers. However, the melt viscosity is too low to be used as a separating claw for copying machines, making it impossible to obtain a smooth radius of curvature at the tip of the separating claw, which sometimes results in sharp edges. Items with high viscosity, specifically those with a melt viscosity of 6000 poise at 300°C (orifice: 1 m in diameter,
2 length, load 10 kg) or more is preferable, and 10
A melt viscosity of 50,000 poise is particularly preferred, and the upper limit of the melt viscosity is not particularly limited as long as melt molding is possible. Boise or less is preferable.
ここで、ポリフェニレンサルファイド樹脂は、たとえば
特公昭44−27671号公報および同45−3368
号公報に開示されているようなハロゲン置換芳香族化合
物と硫化アルカリとの反応、特公昭46−27255号
公報に開示されているような芳香族化合物を塩化硫黄と
のルイス酸触媒共存下における縮合反応、または米国特
許第3274165号に開示されているようなチオフェ
ノール類のアルカリ触媒もしくは銅塩等の共存下におけ
る縮合反応等によって合成されるが、目的に応じて具体
的な方法を任意に選択することが出来る。なお、ポリフ
ェニレンサルファイド樹脂は上記のような縮合等の反応
直後においては白色に近い未架橋品であって、このまま
では低分子量で低粘度であることから、押出成形、射出
成形などの用途に用いるために、空気中において融点以
下に加熱し、酸素架橋させ、または縮合反応の工程で分
子量を高め、抽出成形、駐m射出成形等に適する溶媒粘
度のものに変化させる。このような処理をして溶融成形
用に市販されているライドンP−4(米国フィリップス
・ベトローリアム社製ポリフェニレンサルファイド樹脂
)の溶融粘度は、前述した条件のもとで、1500〜5
000ボイズであるが、 10000ボイズ以上の溶融
粘度のポリフェニレンサルファイド樹脂を得るには、特
に限定するものではないが、たとえば同様の処理を行な
えばよく、たとえば前記ライドンP−4をさらに酸素架
橋させてもよい。また、このような高溶融粘度ポリフェ
ニレンサルファイド樹脂は、トーブレン社のTXOO9
として市販されている。Here, the polyphenylene sulfide resin is disclosed in, for example, Japanese Patent Publication No. 44-27671 and Japanese Patent Publication No. 45-3368.
Reaction of a halogen-substituted aromatic compound with an alkali sulfide as disclosed in Japanese Patent Publication No. 46-27255, condensation of an aromatic compound with sulfur chloride in the presence of a Lewis acid catalyst as disclosed in Japanese Patent Publication No. 46-27255 It is synthesized by a reaction, or a condensation reaction of thiophenols in the presence of an alkali catalyst or a copper salt, etc. as disclosed in U.S. Pat. No. 3,274,165, but a specific method can be arbitrarily selected depending on the purpose. You can. In addition, polyphenylene sulfide resin is an uncrosslinked product that is nearly white immediately after the above-mentioned condensation reaction, etc., and as it is, it has a low molecular weight and low viscosity, so it is suitable for use in extrusion molding, injection molding, etc. First, the molecular weight is increased by heating to below the melting point in air and crosslinking with oxygen, or through a condensation reaction process, and the solvent viscosity is changed to be suitable for extraction molding, injection molding, etc. The melt viscosity of Rydon P-4 (polyphenylene sulfide resin manufactured by Phillips Vetroleum, USA), which is commercially available for melt molding after such treatment, is 1,500 to 5,000 under the above-mentioned conditions.
000 voids, but in order to obtain a polyphenylene sulfide resin with a melt viscosity of 10,000 voids or more, the same treatment may be performed, although not particularly limited. For example, the Rydon P-4 may be further cross-linked with oxygen. Good too. In addition, such high melt viscosity polyphenylene sulfide resin is TXOO9 manufactured by Torblen.
It is commercially available as.
つぎに、この発明における耐熱性繊維とは、ポリフェニ
レンサルファイド樹脂の成形温度(通常280〜350
°C)に耐えることができる繊維を意味し、具体的には
、ガラス繊維、炭素繊維、グラファイト繊維、セラミッ
ク繊維、ロックウール、スラグウール、チタン酸カリウ
ムホイスカー、シリコンカーバイドホイスカー、サファ
イアホイスカ、鋼線、銅線、ステンレス鋼線、炭化ケイ
素繊維、芳香族ポリアミド繊維などを例示することがで
きる。そして、これら繊維の形体は、分離爪成形品の表
面粗さが小さく滑らかで、しかも分離爪先端の曲率半径
の好適範囲としてO,t++w+以下、好ましくは0.
05w以下の精度が必要であることから、繊維径は6μ
以下であることが肝要である。Next, the heat-resistant fiber in this invention refers to the molding temperature of polyphenylene sulfide resin (usually 280 to 350
°C), specifically glass fibers, carbon fibers, graphite fibers, ceramic fibers, rock wool, slag wool, potassium titanate whiskers, silicon carbide whiskers, sapphire whiskers, steel wire Examples include copper wire, stainless steel wire, silicon carbide fiber, and aromatic polyamide fiber. The shape of these fibers is such that the surface roughness of the separated claw molded product is small and smooth, and the radius of curvature of the tip of the separating claw is preferably within O, t++w+, preferably 0.
Since accuracy of 0.05w or less is required, the fiber diameter is 6μ.
It is important that the conditions are as follows.
このような繊維を使用すれば成形品の表面粗さは1〜3
−もしくはそれ以下となり、また分離爪の曲率半径も0
.05■以下となる。さらに、分離爪の高温時の剛性お
よび機械的強度を考慮するならば、繊維長は0.05a
m以上、特に0.1w以上であることが好ましい、また
、相手ローラの攻撃性を考えると硬度の小さいチタン酸
カリウムホイスカー等が好ましいが、これだけでは高温
時の剛性および機械的強度が少し劣るため、前述した繊
維径6n以下で、繊維長0.1鵬以上の繊維類、たとえ
ば、ガラス繊維などを併用することが好ましい。If such fibers are used, the surface roughness of the molded product will be 1 to 3.
- or less, and the radius of curvature of the separation claw is also 0.
.. 05 ■ or less. Furthermore, considering the rigidity and mechanical strength of the separation claw at high temperatures, the fiber length is 0.05a.
m or more, especially 0.1 w or more.Also, considering the aggressiveness of the mating roller, potassium titanate whiskers with small hardness are preferable, but this alone will result in slightly inferior rigidity and mechanical strength at high temperatures. It is preferable to use together the aforementioned fibers having a fiber diameter of 6 nm or less and a fiber length of 0.1 mm or more, such as glass fiber.
そして、これら繊維の配合量は、ポリフェニレンサルフ
ァイド樹脂100重量部に対して20〜200重量部で
ある。なぜならば、配合量が下限値よりも少ないときは
、高温時の剛性および機械的強度が保てなくなるためで
あり、上限値を越える多量では成形時の流動性が極端に
悪化するためである。The blending amount of these fibers is 20 to 200 parts by weight per 100 parts by weight of the polyphenylene sulfide resin. This is because if the amount is less than the lower limit, the rigidity and mechanical strength at high temperatures cannot be maintained, and if the amount exceeds the upper limit, the fluidity during molding will be extremely deteriorated.
既に述べたように、ポリフェニレンサルファイド樹脂と
耐熱性繊維、たとえば、ガラス繊維とからなる組成物を
成形した分離爪は、表面粗さが大きく、先端部の曲率半
径も大きくなり過ぎ、一方、チタン酸カリウムホイスカ
ーのような短繊維で補強した成形品は、高温時の剛性お
よび機械的強度が劣るが、繊維径が6jna以下のもの
を使用するか、または、繊維長が0.1mm以上のもの
を単独で使用するかもしくは併用することによってそれ
ぞれ対処することが可能である。しかし、分離爪先端部
の曲率半径も小さければそれでよいというものではなく
、小さ過ぎてシャープなエツジ(パリ)になったり、金
型加工時に良好な曲率半径のものが得られても、充填剤
等によって金型についた傷跡等のために曲率が非常に小
さくなってシャープなエツジが出現しやすくなったりす
ると、爪先端の高温剛性が小さくなって熱変形を起こし
たり、ローラの外周面を傷つけたりする危険が生じる。As already mentioned, separation claws molded from a composition made of polyphenylene sulfide resin and heat-resistant fibers, such as glass fibers, have a large surface roughness and an excessively large radius of curvature at the tip. Molded products reinforced with short fibers such as potassium whiskers have poor rigidity and mechanical strength at high temperatures, but it is best to use fibers with a diameter of 6JNA or less, or fibers with a length of 0.1mm or more. It is possible to deal with each by using them alone or in combination. However, it is not enough just to have a small radius of curvature at the tip of the separation claw. If the curvature becomes very small and sharp edges are likely to appear due to scars on the mold, etc., the high temperature rigidity of the nail tip will decrease, causing thermal deformation or damaging the outer peripheral surface of the roller. There is a risk of
これに対して、ポリフェニレンサルファイド樹脂と耐熱
性繊維との混合物に耐熱性ポリスルホン樹脂を添加し
た組成物は、このような欠点を解消し、長期にわたって
適度の曲率半径(0,01mg〜0.05■)をもつ分
離爪成形品を得ることができる。ここで、耐熱性ポリス
ルホン樹脂とは、ポリエーテルスルホンおよびポリスル
ホンのように、ポリマーの主鎖中にスルホン結合を有す
る熱可塑性樹脂の中で、耐熱性の高いものが使用される
。On the other hand, heat-resistant polysulfone resin is added to a mixture of polyphenylene sulfide resin and heat-resistant fiber.
The composition overcomes these drawbacks and makes it possible to obtain a separated nail molded product having a suitable radius of curvature (0.01 mg to 0.05 square meters) over a long period of time. Here, the heat-resistant polysulfone resin is a thermoplastic resin having high heat resistance, such as polyether sulfone and polysulfone, which has a sulfone bond in the main chain of the polymer.
ここでいう耐熱性とは、複写機の定着ローラ表面温度(
170〜250°C)で充分に耐え得ることが肝要であ
り、具体的には示差走査熱量計(以下DSCと略記する
)で測定した吸熱開始点(以下onse tと略記する
)におけるガラス転移点が250°C以上であることを
さす。そして、このような耐熱性ポリスルホン樹脂とし
ては、たとえば、英国アイ・シー・アイ社製:ピクトレ
ックス(VICTRI!X) IITA−7600Gが
市販されている。なお、このような耐熱性ポリスルホン
樹脂の添加量は、ポリフェニレンサルファイド樹脂10
0重量部に対して10〜90重量部とすることが望まし
い。なぜならば10重量部未満の少量では、長期にわた
って適度の曲率半径をもった分離爪成形品を得ることが
できず、また逆に90重量部を越える多量では、ポリフ
ェニレンサルファイド樹脂との相溶性が悪化して機械的
強度の低下を起こし好ましくないからである。なお、ポ
リフェニレンサルファイド樹脂と耐熱性ポリスルホン樹
脂との相溶性をさらに増すために、ポリフェニレンスル
フィド部分とポリスルホン部分とからなる共重合体、ま
たはポリマー分子中に繰り香族サルファイド/スルホン
ポリマーを添加してもよい、さらに、この発明の目的を
損なわない範囲内で、接着性向上剤、チクソトロピー性
付与剤を配合することは好ましく、また、その他各種充
填剤を配合してもよい、ここで、接着性向上剤とは、ト
ナーに対する非粘着性を向上させるために分離爪成形体
表面に被覆させるコーティング剤と分離爪成形体との間
の密着強度を上げるために添加されるもので、たとえば
、エポキシ基、カルボキシル基、水酸基、フェノキシ基
、メチロール基、アミノ基のうちの少なくとも一つの基
を有する熱硬化性樹脂が好適であって、具体的にはフェ
ノール樹脂またはエポキシ樹脂を挙げることができる。Heat resistance here refers to the surface temperature of the fusing roller of the copier (
It is important that the glass transition point at the endothermic onset point (hereinafter abbreviated as "onset") measured with a differential scanning calorimeter (hereinafter abbreviated as DSC) is essential. is 250°C or higher. As such a heat-resistant polysulfone resin, for example, VICTRI! The amount of heat-resistant polysulfone resin added is 10% of polyphenylene sulfide resin.
It is desirable that the amount is 10 to 90 parts by weight relative to 0 parts by weight. This is because if the amount is less than 10 parts by weight, it will not be possible to obtain a separated claw molded product with an appropriate radius of curvature over a long period of time, and if the amount is more than 90 parts by weight, the compatibility with the polyphenylene sulfide resin will deteriorate. This is because it causes a decrease in mechanical strength, which is undesirable. In addition, in order to further increase the compatibility between polyphenylene sulfide resin and heat-resistant polysulfone resin, a copolymer consisting of a polyphenylene sulfide moiety and a polysulfone moiety, or a aromatic sulfide/sulfone polymer may be added to the polymer molecule. Furthermore, it is preferable to blend an adhesion improver and a thixotropy imparting agent within a range that does not impair the purpose of the present invention, and various other fillers may also be blended. The agent is added to increase the adhesion strength between the coating agent coated on the surface of the separated nail molded object and the separated nail molded object in order to improve non-adhesiveness to toner, and includes, for example, an epoxy group, A thermosetting resin having at least one group selected from a carboxyl group, a hydroxyl group, a phenoxy group, a methylol group, and an amino group is suitable, and specific examples thereof include phenol resins and epoxy resins.
また、チクソトロピー性付与剤とは、この発明の組成物
が溶融する際に、低剪断速度において増粘効果をもたら
すものをいい、具体的には微粉末シリカ、微粉末タルク
、珪藻上等が挙げられ、これらを添加することによって
分離爪の先端形状の真直度および曲率半径のバラツキが
さらに良好となる。また、これら以外の充填剤としては
、通常の樹脂組成物に添加される酸化防止剤、熱安定剤
、紫外線吸収剤、滑剤、離型剤、着色剤、I燃剤、難燃
助剤、帯電防止剤などのほかに、耐摩耗性向上剤(たと
えば、グラファイト、カーボランダム、珪石粉、二硫化
モリブデン、フッ素樹脂など)、耐トラツキング性向上
剤(たとえば、シリカ、グラファイトなど)その他充填
剤(たとえば、ガラスピーズ、ガラスバルーン、炭酸カ
ルシウム、アルミナ、タルク、珪藻土、クレー、カオリ
ン、石膏、亜硫酸カリシラム、マイカ、金属酸化物、無
機質顔料など、300°C以上で安定な物質)などを挙
げることができる。In addition, the thixotropic agent refers to an agent that provides a thickening effect at a low shear rate when the composition of the present invention is melted, and specific examples thereof include finely powdered silica, finely powdered talc, and diatoms. By adding these, the straightness and the variation in the radius of curvature of the tip shape of the separation claw can be further improved. In addition, fillers other than these include antioxidants, heat stabilizers, ultraviolet absorbers, lubricants, mold release agents, colorants, I flame agents, flame retardant aids, and antistatic agents that are added to ordinary resin compositions. In addition to additives, wear resistance improvers (e.g., graphite, carborundum, silica powder, molybdenum disulfide, fluorine resins, etc.), tracking resistance improvers (e.g., silica, graphite, etc.), and other fillers (e.g., Examples include glass peas, glass balloons, calcium carbonate, alumina, talc, diatomaceous earth, clay, kaolin, gypsum, calicylum sulfite, mica, metal oxides, inorganic pigments, and other substances that are stable at temperatures above 300°C.
(作用)
分離爪の高温時における剛性および機械的強度を増強さ
せるために添加する耐熱性繊維の平均繊維径を6μ−以
下とすることによって、先端部の曲率半径および表面平
滑性への悪影響を防ぎ、さらに耐熱性ポリスルホン樹脂
を添加することによって、従来の技術による分離爪にお
いて、滑らかな曲線が得られなかったり、時としてシャ
ープなエツジ(バリ)になったり、たとえ金型加工時に
良好な曲率半径のものが得られても、長時間使用の過程
で樹脂からでる腐食性ガスまたは配合されている充填剤
などによって金型についた傷跡などのために、分離爪の
先端形状が悪くなったり、曲率半径も非常に小さくなっ
てシャープなエツジが出現しやすくなりたりして、長期
にわたって適度の曲率半径の維持できる成形品が得られ
なかったという欠点を払拭し、ポリフェニレンサルファ
イド樹脂の優れた耐熱性または複雑なもしくは薄肉の部
位にも容易に成形できる優れた成形性を阻害することな
く、低価格で捷供できるものである。(Function) By setting the average fiber diameter of the heat-resistant fibers added to increase the rigidity and mechanical strength of the separation claw at high temperatures to 6μ or less, the adverse effect on the radius of curvature and surface smoothness of the tip can be avoided. Furthermore, by adding heat-resistant polysulfone resin, it is possible to prevent smooth curves or sometimes sharp edges (burrs) in separating claws using conventional technology, and even if good curvature is not achieved during mold processing. Even if a radius is obtained, the shape of the tip of the separating claw may deteriorate due to scars on the mold caused by corrosive gases emitted from the resin or fillers that are mixed during long-term use. The radius of curvature becomes very small and sharp edges tend to appear, making it impossible to obtain molded products that can maintain an appropriate radius of curvature over a long period of time. Alternatively, it can be manufactured at a low cost without impairing its excellent moldability, which allows it to be easily molded into complex or thin-walled parts.
実施例および比較例に使用した原材料を一括して示すと
つぎのとおりであり、〔]内にそれぞれの略号を示した
。なお、これら原材料の配合はすべて1ltfft部で
表わした。The raw materials used in the Examples and Comparative Examples are collectively shown below, and the respective abbreviations are shown in [ ]. Note that all the formulations of these raw materials are expressed in 1ltfft parts.
■ ポリフェニレンサルファイドNON (PPS−1
3(米国フィリップス・ペトローリアム社製:ライトン
P−4、溶融粘度2000ポイズ)、■ ポリフェニレ
ンサルファイド樹脂(PPS−2)(呉羽化学工業社製
: KPSI214、溶融粘度2000ボイズ)、
■ ポリフェニレンサルファイド樹脂(PPS−3)(
トーブレン社製二 Tに009、溶融粘度10000ボ
イズ)、
■ 耐熱性ポリスルホン樹脂(HTA)(英国アイ・シ
ー・アイ社製:ピクトレックス)ITA7600G、ガ
ラス転移点260’C(DSC法、onset))、■
ポリエーテルスルホン樹脂(PES)(英国アイ・シ
ー・アイ社製:ピクトレックスPE54800P、ガラ
ス転移点220℃CD5C法、onset) )、■
ポリアミドイミド樹脂(FAI)
(米国アミコ社製ニドーロン(Torlon) 40
00T。■ Polyphenylene sulfide NON (PPS-1
3 (manufactured by Phillips Petroleum, USA: Ryton P-4, melt viscosity 2000 poise), ■ Polyphenylene sulfide resin (PPS-2) (manufactured by Kureha Chemical Industry Co., Ltd.: KPSI214, melt viscosity 2000 poise), ■ Polyphenylene sulfide resin (PPS) -3)(
Heat-resistant polysulfone resin (HTA) (Pictrex, manufactured by ICI, UK) ITA7600G, glass transition point 260'C (DSC method, onset)) ,■
Polyether sulfone resin (PES) (manufactured by ICI UK: Pictrex PE54800P, glass transition point 220°C CD5C method, onset)), ■
Polyamideimide resin (FAI) (Torlon 40 manufactured by Amico, USA)
00T.
ガラス転移点260°C(DSC法、onset) )
、■ ガラス繊維(GF−33
(旭ファイバーグラス社製:チッップドストランド、繊
維径3趨、繊維長3閣、アミノシランカップリング処理
品)、
■ ガラス繊維(GF−6)
(旭ファイバーグラス社製:チョップドストランド、繊
維径6μ転繊維長3■、アミノシランカップリング処理
品)、
■ ガラス繊維(GF−13)
(旭ファイバーグラス社製:チョップドストランド、繊
維径13Q、繊維長3m、アミノシランカップリング処
理品)、
[相] チタン酸カリウムホイスカー(PTW)(大塚
化学社製:ティスモD102、繊維径0.1〜0.3μ
m、繊維長20〜30IllII)、■ 炭素繊維(C
F−8)
(東邦レーヨン社製:ベスファイトIITA、繊維径7
.2μ■、繊維長6am)、
以上の樹脂原料の内、■耐熱性ポリスルホン樹MW (
tlTA)については冷凍粉砕機を用いてベレットを平
均粒径50Xmに粉砕して使用した。Glass transition point 260°C (DSC method, onset)
, ■ Glass fiber (GF-33 (manufactured by Asahi Fiberglass Co., Ltd.: chipped strand, 3 fiber diameters, 3 fiber lengths, aminosilane coupling treated product), ■ Glass fiber (GF-6) (Asahi Fiberglass) Made by Asahi Fiberglass Co., Ltd.: Chopped strand, fiber diameter 6μ, fiber length 3mm, aminosilane coupling treated product), Glass fiber (GF-13) (Made by Asahi Fiberglass Co., Ltd.: chopped strand, fiber diameter 13Q, fiber length 3m, aminosilane cup) Ring treated product), [Phase] Potassium titanate whisker (PTW) (manufactured by Otsuka Chemical Co., Ltd.: Tismo D102, fiber diameter 0.1-0.3μ
m, fiber length 20-30IllII), ■ Carbon fiber (C
F-8) (Manufactured by Toho Rayon Co., Ltd.: Besphite IITA, fiber diameter 7
.. 2μ■, fiber length 6am), among the above resin raw materials, ■heat-resistant polysulfone resin MW (
tlTA) was used by pulverizing pellets to an average particle size of 50×m using a freezing pulverizer.
実施例1〜8:
第1表に示す配合割合で各原材料を予め乾式混合した後
、二軸溶融押出機(部員鉄工社製: P(M−30)に
供給し、シリンダー温度290〜320’C,スクリュ
ー回転数5Orpm+の条件下で混練押出しして造粒し
た。得られたベレットをシリンダー温度310〜340
’C1射出圧800kg/cd、金型温度130″Cの
条件のもとに射出成形し、幅12.7m、長さ126■
、厚さ3.2mの板材、幅41m1、長さ25a、厚さ
工■の板材および富士ゼロックス社製複写12700型
に用いられている分離爪と同一形状の試験片を得た。こ
れらの試験片のうち、分離の良不良およびローラの損傷
性の実用的機能性調査用に作製した分離爪試験片につい
ては、すべて端末にイソシアネート基をもったフッ素化
ポリエーテル重合体(伊国モンテジソン社製:フォンプ
リンZ−DISOC2000)を2.0重量%濃度に溶
解したフレオン113溶液中に浸漬した後、液から取り
出して約200’Cで2時間焼付は処理を施した。Examples 1 to 8: After dry-mixing each raw material in the proportions shown in Table 1, it was supplied to a twin-screw melt extruder (P (M-30) manufactured by Munen Tekko Co., Ltd., and the cylinder temperature was 290 to 320'. C. Pelletization was performed by kneading and extrusion at a screw rotation speed of 5 Orpm+.The resulting pellets were heated at a cylinder temperature of 310 to 340.
Injection molded under the conditions of 'C1 injection pressure 800kg/cd and mold temperature 130''C, width 12.7m, length 126mm
, a test piece having a thickness of 3.2 m, a width of 41 m1, a length of 25 a, a thickness of 1, and a separation claw having the same shape as that used in a copying machine 12700 manufactured by Fuji Xerox Co., Ltd. was obtained. Among these test pieces, the separation claw test pieces prepared for practical functionality investigation of separation quality and roller damage were all made of fluorinated polyether polymer with isocyanate groups at the terminals (Italian). After immersing a Freon 113 solution (manufactured by Montageson) in a Freon 113 solution at a concentration of 2.0% by weight, the sample was taken out of the solution and baked at about 200'C for 2 hours.
以上の試験片に約して曲げ強度、高温時の剛性(弾性率
の保持率)、先端の曲率半径、表面平滑性および実用的
機能性を評価した。これらの評価方法はそれぞれつぎの
とおりである。The above test pieces were evaluated for bending strength, stiffness at high temperatures (retention rate of elastic modulus), radius of curvature of the tip, surface smoothness, and practical functionality. These evaluation methods are as follows.
1)曲げ強度 ASTM−[1790に基づく。1) Bending strength Based on ASTM-[1790.
2)高温時の剛性(弾性率の保持率)
東洋精機製作所型の動的粘弾性測定装置を用いて、幅4
II1m、長さ25m、厚さIIIIlの試験片を使っ
て、周波数10Hzで引張り応力を加え、温度変化にも
の(○印)および15−を越えるもの(Δ印)の3段階
に評価した。2) Stiffness at high temperatures (retention rate of elastic modulus) Using a Toyo Seiki Seisakusho type dynamic viscoelasticity measuring device,
Using a test piece of II1 m, length 25 m, and thickness IIIl, tensile stress was applied at a frequency of 10 Hz, and the temperature change was evaluated in three stages: those with a temperature change (○ mark) and those exceeding 15 - (Δ mark).
以上の諸試験で得られた結果を第2表にまとめた。The results obtained from the above tests are summarized in Table 2.
第2表
比較例1〜7:
第3表に示す割合で各原材料を配合した以外は実施例1
と全く同じ操作を行なって試験片を作製し、実施例1〜
8におけると同じ緒特性を調べた。Table 2 Comparative Examples 1 to 7: Example 1 except that each raw material was blended in the proportions shown in Table 3.
A test piece was prepared by performing exactly the same operation as in Example 1 to
The same characteristics as in 8 were investigated.
得られた結果を第4表にまとめた。The results obtained are summarized in Table 4.
対する引張り弾性率の変化を25°Cおよび250℃で
求めた。The change in tensile modulus was determined at 25°C and 250°C.
3)先端の曲率半径
日本光学社製の投影器V−160を使用し、n=100
における測定値の最小および最大の範囲で示した。3) Radius of curvature at the tip Using projector V-160 manufactured by Nippon Kogaku Co., Ltd., n = 100
The minimum and maximum range of measured values is shown.
だたし5趨より小さいものは、精度よく測定できないた
め1μと記した。However, since it is not possible to accurately measure values smaller than 5, they are marked as 1μ.
4)表面平滑性
表面粗さ計(日本真空社製: Dektak II型)
を使用し、分離爪のローラ接触部の表面粗さを測定した
。4) Surface smoothness surface roughness meter (manufactured by Nippon Shinku Co., Ltd.: Dektak II type)
was used to measure the surface roughness of the roller contact area of the separation claw.
5)実用的機能
乾式複写機(富士ゼロックス社製: 2700型)を用
い、それに使用されている分離爪と同一形状の試験片を
取り付けて、84判の複写用紙5万枚を連続通紙した。5) Using a practical functional dry copying machine (Model 2700, manufactured by Fuji Xerox Co., Ltd.), a test piece with the same shape as the separating claw used in the machine was attached, and 50,000 sheets of 84-size copy paper were continuously passed through. .
複写を繰り返し、紙の分離不良(祇詰り)の起こった時
点の複写枚数および相手ローラの損傷の程度を、表面粗
さ計を用いて、分離爪摺接部の運転前後の形伏f!認を
行ない、ローラの摩耗深さが5μ未満のもの(◎印)、
5〜15−の第3表
第4表
第2表および第4表からつぎのことかいえる。Copying is repeated, and the number of copies and the degree of damage to the mating roller at the time when paper separation failure (jamming) occurs is measured using a surface roughness meter, and the shape of the separation pawl contact area before and after operation f! The wear depth of the roller is less than 5μ (marked with ◎).
The following can be said from Tables 2 and 4 of Tables 3 and 4 of 5-15-.
すなわち、実施例1〜8は曲げ強度がよく、高温時の引
張り弾性率(高温時の剛性)、先端曲率半径の精度およ
び表面平滑性はいずれも良好な値を示している。これに
対して繊維径6nのガラス繊維を使用していても、耐熱
性ポリスルホン樹脂を併用していない比較例1および耐
熱性ポリスルホン樹脂は使用しても、耐熱性繊維の平均
繊維径が6nを越えるものを使用した比較例6または7
は、曲げ強度、引張弾性率等は実施例と同等の良い値を
示してはいるが、先端曲率半径が小さ(なり過ぎていわ
ゆるパリを生じ好ましくない、比較例6と7においては
さらに、太い繊w1類の悪影響から曲率半径が大き過ぎ
るものもあり好ましくなく、表面平滑性も悪い、また、
比較例2はガラス転移点が250°C以下で220°C
のポリスルホン樹脂を使用したものであるが、高温での
引張り弾性率が極端に悪い、さらにガラス転移点が25
0℃以上であっても、耐熱性ポリサルホン以外の樹脂で
あるポリアミドイミド樹脂を用いた比較例3は、曲げ強
度、高温時の引張り弾性率の値はそれ程悪くないが、パ
リ発生のものから不充填ぎみのものまで先端曲率半径の
バラツキが大きく、また表面の平滑性も悪い、これはお
そら(母材のポリフェニレンサルファイド樹脂とポリア
ミドイミド樹脂との相溶性が非常に悪いためだと思われ
る。また、耐熱性ポリスルホン樹脂の添加量が多過ぎる
比較例4も、比較例3と同様に相溶性が低下する結果、
曲げ強度が小さくなり、先端曲率半径のバラツキが大き
くなって、パリが発生するものから不充填のものまで生
じる。また、耐熱性繊維の添加量が少な過ぎる比較例5
は、補強効果が小さ過ぎるため、曲げ強度が小さ過ぎ、
高温での剛性も小さく、曲率半径においても小さなもの
がある。That is, Examples 1 to 8 have good bending strength, and the tensile modulus at high temperature (rigidity at high temperature), accuracy of tip curvature radius, and surface smoothness all show good values. On the other hand, even if glass fibers with a fiber diameter of 6n are used, the average fiber diameter of the heat-resistant fibers is 6n even if heat-resistant polysulfone resin is used and in Comparative Example 1 where heat-resistant polysulfone resin is not used. Comparative example 6 or 7 using something that exceeds
Although the bending strength, tensile modulus, etc. of the samples shown in Comparative Examples 6 and 7 were as good as those of the examples, the radius of curvature of the tip was too small (too large, resulting in so-called "burr"), which was undesirable. Due to the adverse effects of fibers W1, some have too large a radius of curvature, which is undesirable, and the surface smoothness is also poor.
Comparative example 2 has a glass transition point of 250°C or lower and 220°C.
However, the tensile modulus at high temperatures is extremely poor, and the glass transition point is 25.
Even at temperatures above 0°C, the bending strength and tensile modulus at high temperatures of Comparative Example 3 using polyamideimide resin, which is a resin other than heat-resistant polysulfone, were not so bad, but they were not as bad as those with paris generation. The radius of curvature of the tip varies greatly even when it is almost filled, and the surface smoothness is also poor. This is probably due to the extremely poor compatibility between the base material polyphenylene sulfide resin and polyamideimide resin. Similarly to Comparative Example 3, Comparative Example 4 in which the amount of heat-resistant polysulfone resin added was too large resulted in a decrease in compatibility.
The bending strength decreases, and the dispersion of the radius of curvature at the tip increases, resulting in cases ranging from those with cracks to those with no filling. Also, Comparative Example 5 in which the amount of heat-resistant fiber added is too small.
Because the reinforcement effect is too small, the bending strength is too small.
Some have low rigidity at high temperatures and a small radius of curvature.
このように比較例1〜7は、曲げ強度、高温時の剛性、
先端曲率半径、表面平滑性などについてすべてを満足し
ているものがないことから、実用的機能においても、分
離不良を起こすことなく5万枚の複写を完了したものは
なく、また比較例2のように分離不良があまりにも早く
起こったために、ローラの損傷性が少ないものは別とし
て、その他の比較例はすべて相手ローラの損傷性も良く
なかった。In this way, Comparative Examples 1 to 7 have bending strength, rigidity at high temperature,
Since there is no product that satisfies all aspects such as tip radius of curvature and surface smoothness, there is no product that has completed copying of 50,000 sheets without causing separation defects even in terms of practical functions, and Comparative Example 2 Because the separation failure occurred too quickly, in all other comparative examples, the damage to the mating roller was also poor, except for the one in which the roller was less likely to be damaged.
以上述べたように、この発明のポリフェニレンサルファ
イド樹脂と平均繊維径6n以下の耐熱性繊維と耐熱性ポ
リスルホン樹脂とを必須成分とする材料からなる複写機
用分離爪は、機械的強度、高温時の剛性に優れ、分離爪
先端曲率半径が小さ過ぎたり、大き過ぎたりすることに
よる祇詰りまたは分離方向不良を起こすことなく、また
表面が平滑であるため、分離紙が引っ掛かることなく、
必要に応じてさらにフッ素化ポリエーテル重合体等の非
粘着性被膜を施すことによって、良好な分離爪形状その
ままに優れた非粘着性を実現することが出来る結果、長
期連続使用に充分耐えうるちのである。このような特性
をポリフェニレンサルファイド樹脂の優れた成形性をそ
のままに、低価格で実現するものであるから、この発明
の意義はきわめて大きいということが出来る。As described above, the separation claw for a copying machine made of a material containing polyphenylene sulfide resin, heat-resistant fibers with an average fiber diameter of 6 nm or less, and heat-resistant polysulfone resin as essential components has excellent mechanical strength and It has excellent rigidity and does not cause clogging or poor separation direction due to the radius of curvature at the tip of the separation claw being too small or large, and because the surface is smooth, the separation paper will not get caught.
If necessary, by applying a non-adhesive coating such as fluorinated polyether polymer, it is possible to achieve excellent non-adhesive properties while retaining the good separation claw shape, resulting in a film that can withstand long-term continuous use. It is. The significance of this invention is extremely great because it achieves these characteristics at a low cost while maintaining the excellent moldability of polyphenylene sulfide resin.
Claims (1)
平均繊維径6μm以下の耐熱性繊維20〜200重量部
および耐熱性ポリスルホン樹脂10〜90重量部を必須
成分とするポリフェニレンサルファイド樹脂組成物の成
形品であることを特徴とする複写機用分離爪。(1) 100 parts by weight of polyphenylene sulfide resin,
A separating claw for a copying machine, characterized in that it is a molded article of a polyphenylene sulfide resin composition containing 20 to 200 parts by weight of heat-resistant fibers with an average fiber diameter of 6 μm or less and 10 to 90 parts by weight of a heat-resistant polysulfone resin.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6814989A JP2843355B2 (en) | 1989-03-20 | 1989-03-20 | Separation claw for copier |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6814989A JP2843355B2 (en) | 1989-03-20 | 1989-03-20 | Separation claw for copier |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH02247678A true JPH02247678A (en) | 1990-10-03 |
JP2843355B2 JP2843355B2 (en) | 1999-01-06 |
Family
ID=13365397
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP6814989A Expired - Fee Related JP2843355B2 (en) | 1989-03-20 | 1989-03-20 | Separation claw for copier |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2843355B2 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5837366A (en) * | 1996-07-08 | 1998-11-17 | Ntn Corporation | Stripping fingers for copying machines and printers |
JP2011008103A (en) * | 2009-06-26 | 2011-01-13 | Ntn Corp | Sheet-like peeling member for electrophotographic device, and the electrophotographic device |
-
1989
- 1989-03-20 JP JP6814989A patent/JP2843355B2/en not_active Expired - Fee Related
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5837366A (en) * | 1996-07-08 | 1998-11-17 | Ntn Corporation | Stripping fingers for copying machines and printers |
JP2011008103A (en) * | 2009-06-26 | 2011-01-13 | Ntn Corp | Sheet-like peeling member for electrophotographic device, and the electrophotographic device |
Also Published As
Publication number | Publication date |
---|---|
JP2843355B2 (en) | 1999-01-06 |
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