JPH02232252A - Phenol resin drum base material - Google Patents
Phenol resin drum base materialInfo
- Publication number
- JPH02232252A JPH02232252A JP5205889A JP5205889A JPH02232252A JP H02232252 A JPH02232252 A JP H02232252A JP 5205889 A JP5205889 A JP 5205889A JP 5205889 A JP5205889 A JP 5205889A JP H02232252 A JPH02232252 A JP H02232252A
- Authority
- JP
- Japan
- Prior art keywords
- phenol resin
- base material
- phenolic resin
- drum base
- acid amide
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 239000005011 phenolic resin Substances 0.000 title claims abstract description 54
- 239000000463 material Substances 0.000 title claims abstract description 29
- 239000000314 lubricant Substances 0.000 claims abstract description 28
- 238000001125 extrusion Methods 0.000 claims abstract description 22
- 239000000654 additive Substances 0.000 claims abstract description 9
- 235000014113 dietary fatty acids Nutrition 0.000 claims abstract description 9
- 239000000194 fatty acid Substances 0.000 claims abstract description 9
- 229930195729 fatty acid Natural products 0.000 claims abstract description 9
- 150000004665 fatty acids Chemical class 0.000 claims abstract description 9
- 229920001568 phenolic resin Polymers 0.000 claims description 39
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 claims description 38
- 239000000203 mixture Substances 0.000 claims description 19
- 239000011256 inorganic filler Substances 0.000 claims description 9
- 229910003475 inorganic filler Inorganic materials 0.000 claims description 9
- 239000012766 organic filler Substances 0.000 claims description 9
- 229920005989 resin Polymers 0.000 claims description 8
- 239000011347 resin Substances 0.000 claims description 8
- 238000002844 melting Methods 0.000 claims description 7
- 230000008018 melting Effects 0.000 claims description 7
- 238000002156 mixing Methods 0.000 claims description 4
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 2
- 239000000945 filler Substances 0.000 abstract description 3
- HSEMFIZWXHQJAE-UHFFFAOYSA-N hexadecanamide Chemical compound CCCCCCCCCCCCCCCC(N)=O HSEMFIZWXHQJAE-UHFFFAOYSA-N 0.000 abstract description 2
- VKOBVWXKNCXXDE-UHFFFAOYSA-N icosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCC(O)=O VKOBVWXKNCXXDE-UHFFFAOYSA-N 0.000 abstract description 2
- LYRFLYHAGKPMFH-UHFFFAOYSA-N octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(N)=O LYRFLYHAGKPMFH-UHFFFAOYSA-N 0.000 abstract description 2
- 230000000740 bleeding effect Effects 0.000 abstract 1
- 238000013329 compounding Methods 0.000 abstract 1
- 239000002932 luster Substances 0.000 abstract 1
- 238000000034 method Methods 0.000 description 8
- 239000000835 fiber Substances 0.000 description 7
- VKYKSIONXSXAKP-UHFFFAOYSA-N hexamethylenetetramine Chemical compound C1N(C2)CN3CN1CN2C3 VKYKSIONXSXAKP-UHFFFAOYSA-N 0.000 description 6
- 108091008695 photoreceptors Proteins 0.000 description 6
- 239000011342 resin composition Substances 0.000 description 6
- 230000000704 physical effect Effects 0.000 description 5
- 229910052782 aluminium Inorganic materials 0.000 description 4
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 238000004898 kneading Methods 0.000 description 4
- 238000000465 moulding Methods 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 239000003086 colorant Substances 0.000 description 3
- 239000004312 hexamethylene tetramine Substances 0.000 description 3
- 235000010299 hexamethylene tetramine Nutrition 0.000 description 3
- -1 linters Polymers 0.000 description 3
- 230000001050 lubricating effect Effects 0.000 description 3
- 239000010680 novolac-type phenolic resin Substances 0.000 description 3
- 239000004014 plasticizer Substances 0.000 description 3
- 229920003987 resole Polymers 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical class O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000000748 compression moulding Methods 0.000 description 2
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 2
- 238000009778 extrusion testing Methods 0.000 description 2
- 239000003063 flame retardant Substances 0.000 description 2
- HYBBIBNJHNGZAN-UHFFFAOYSA-N furfural Chemical compound O=CC1=CC=CO1 HYBBIBNJHNGZAN-UHFFFAOYSA-N 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 229920003986 novolac Polymers 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 238000010298 pulverizing process Methods 0.000 description 2
- 239000011134 resol-type phenolic resin Substances 0.000 description 2
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000001721 transfer moulding Methods 0.000 description 2
- BGJSXRVXTHVRSN-UHFFFAOYSA-N 1,3,5-trioxane Chemical compound C1OCOCO1 BGJSXRVXTHVRSN-UHFFFAOYSA-N 0.000 description 1
- MFYSUUPKMDJYPF-UHFFFAOYSA-N 2-[(4-methyl-2-nitrophenyl)diazenyl]-3-oxo-n-phenylbutanamide Chemical compound C=1C=CC=CC=1NC(=O)C(C(=O)C)N=NC1=CC=C(C)C=C1[N+]([O-])=O MFYSUUPKMDJYPF-UHFFFAOYSA-N 0.000 description 1
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 229920000049 Carbon (fiber) Polymers 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- ORAWFNKFUWGRJG-UHFFFAOYSA-N Docosanamide Chemical compound CCCCCCCCCCCCCCCCCCCCCC(N)=O ORAWFNKFUWGRJG-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 102000006835 Lamins Human genes 0.000 description 1
- 108010047294 Lamins Proteins 0.000 description 1
- 229930040373 Paraformaldehyde Natural products 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- YSMRWXYRXBRSND-UHFFFAOYSA-N TOTP Chemical compound CC1=CC=CC=C1OP(=O)(OC=1C(=CC=CC=1)C)OC1=CC=CC=C1C YSMRWXYRXBRSND-UHFFFAOYSA-N 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 229920002978 Vinylon Polymers 0.000 description 1
- AUNAPVYQLLNFOI-UHFFFAOYSA-L [Pb++].[Pb++].[Pb++].[O-]S([O-])(=O)=O.[O-][Cr]([O-])(=O)=O.[O-][Mo]([O-])(=O)=O Chemical compound [Pb++].[Pb++].[Pb++].[O-]S([O-])(=O)=O.[O-][Cr]([O-])(=O)=O.[O-][Mo]([O-])(=O)=O AUNAPVYQLLNFOI-UHFFFAOYSA-L 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 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
- 229910000410 antimony oxide Inorganic materials 0.000 description 1
- 239000004760 aramid Substances 0.000 description 1
- 229920003235 aromatic polyamide Polymers 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000010425 asbestos Substances 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000004917 carbon fiber Substances 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 230000002844 continuous effect Effects 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 229930003836 cresol Natural products 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- DGVMNQYBHPSIJS-UHFFFAOYSA-N dimagnesium;2,2,6,6-tetraoxido-1,3,5,7-tetraoxa-2,4,6-trisilaspiro[3.3]heptane;hydrate Chemical compound O.[Mg+2].[Mg+2].O1[Si]([O-])([O-])O[Si]21O[Si]([O-])([O-])O2 DGVMNQYBHPSIJS-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000004049 embossing Methods 0.000 description 1
- 150000002085 enols Chemical class 0.000 description 1
- 235000012438 extruded product Nutrition 0.000 description 1
- 239000002657 fibrous material Substances 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 235000019256 formaldehyde Nutrition 0.000 description 1
- 239000008098 formaldehyde solution Substances 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- LUOABWGXXKLFGZ-UHFFFAOYSA-N hexacosanamide Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCC(N)=O LUOABWGXXKLFGZ-UHFFFAOYSA-N 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- 239000012784 inorganic fiber Substances 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011147 inorganic material Substances 0.000 description 1
- 229910052742 iron Inorganic materials 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
- 210000005053 lamin Anatomy 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 1
- 239000000347 magnesium hydroxide Substances 0.000 description 1
- 229910001862 magnesium hydroxide Inorganic materials 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- 239000007769 metal material Substances 0.000 description 1
- 239000011490 mineral wool Substances 0.000 description 1
- 239000012778 molding material Substances 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- MYSPBSKLIFPWDI-UHFFFAOYSA-N octacosanamide Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCC(N)=O MYSPBSKLIFPWDI-UHFFFAOYSA-N 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- VTRUBDSFZJNXHI-UHFFFAOYSA-N oxoantimony Chemical compound [Sb]=O VTRUBDSFZJNXHI-UHFFFAOYSA-N 0.000 description 1
- 229920002866 paraformaldehyde Polymers 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 229910052895 riebeckite Inorganic materials 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 238000004513 sizing Methods 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- PRVCAOGWEXDDOF-UHFFFAOYSA-N tris(2,3-dibromobutyl) phosphate Chemical compound CC(Br)C(Br)COP(=O)(OCC(Br)C(C)Br)OCC(Br)C(C)Br PRVCAOGWEXDDOF-UHFFFAOYSA-N 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
- 125000002256 xylenyl group Chemical class C1(C(C=CC=C1)C)(C)* 0.000 description 1
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、特に電子写真複写機やファクシミリ等の静電
記録装置に使用される浮き出しの改良された感光体用フ
ェノール系樹脂ドラム基材に関する.
〔従来の技術}
フェノール系樹脂成形品は、熱可塑性用脂成形品に比較
して熱時の機械的強度に優れ、その上他の熱硬化性樹脂
と比較しても、機械的強度、電気的特性、耐熱性、H燃
性、物理的特性、化学的特性に優れ、かつ比較的安価な
ことから、圧縮成形法、トランスファー成形法、射出成
形法、押出成形法等で製造され、各々の成形法に適した
樹脂組成物が用いられている.
これらのフェノール系樹脂組成物の成形法のうち、押出
成形法は、プランジャー押出法とスクリュー押出法とが
開発されている.
良好な表面光沢と形状精度を要求される感光体用ドラム
基材は、従来、鉄、ステンレス、銅、アルミニウム、錫
等の金属材料で製造されているが、特に軽量で加工性に
優れているアルミニウムが主に用いられている.アルミ
ニウムをドラム基材に用いるためには、形状と寸法精度
を得るため機械加工を行った後、鏡面加工が施される.
また、この加工時に付着した油や異物等の除去が必要で
あり、製造工程が繁雑となる.しかも、アルミニウムの
表面は非常に活性であり、酸化されてアルマイト系酸化
膜が生じやすく酸化を防止する必要があるという問題点
を有していた.
これらの欠点を解決し、優れた各種特性を存した、安価
な樹脂のドラム基材が望まれている.例えば、フェノー
ル系樹脂組成物の連続押出成形法で樹脂のドラム基材の
製造が可能である.ブランジャー押出成形法は、ドラム
状物等の単調な形状の長尺押出製品の生産に利用されて
いる。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a phenolic resin drum base material for a photoreceptor with improved embossing, particularly used in electrostatic recording devices such as electrophotographic copying machines and facsimile machines. .. [Prior art] Phenolic resin molded products have superior mechanical strength when heated compared to thermoplastic resin molded products, and also have superior mechanical strength and electrical strength compared to other thermosetting resins. It has excellent physical properties, heat resistance, hydrogen flammability, physical properties, and chemical properties, and is relatively inexpensive, so it is manufactured by compression molding, transfer molding, injection molding, extrusion, etc. A resin composition suitable for the molding method is used. Among the methods for molding these phenolic resin compositions, two extrusion methods have been developed: a plunger extrusion method and a screw extrusion method. Photoreceptor drum base materials, which require good surface gloss and shape accuracy, have traditionally been manufactured from metal materials such as iron, stainless steel, copper, aluminum, and tin, but these materials are particularly lightweight and have excellent workability. Aluminum is mainly used. In order to use aluminum as a drum base material, it is machined to obtain shape and dimensional accuracy, and then mirror-finished.
In addition, it is necessary to remove oil and foreign substances that adhere to the product during this processing, which complicates the manufacturing process. Moreover, the surface of aluminum is very active and tends to be oxidized to form an alumite oxide film, which is a problem in that oxidation must be prevented. There is a need for an inexpensive resin drum base material that overcomes these drawbacks and has various excellent properties. For example, it is possible to manufacture a resin drum base material by continuous extrusion molding of a phenolic resin composition. The Blunger extrusion method is used to produce long extruded products with monotonous shapes, such as drum-shaped products.
然しながら、ブランジャー押出成形装置においては、金
型部における押出圧が高く、しかも間欠押出であるため
良好な表面光沢と形状精度を有する均一な成形品を得る
ことが困難であり生産性も低い.
かかる事情から、所謂スクリュー型押出成形装置を用い
る成形法が開発されている.これは、押出機内で混練熔
融されたフェノール系樹脂組成物をアダプターを通じて
、金型内へ導き最終形状に賦形する装置である.
然しなから、従来のフェノール系樹脂組成物では金型部
における押出圧が高く、また、組成物の流路が?XHに
変化し、僅かな温度や圧力の差でフェノール系樹脂組成
物の硬化反応が急激に進行したり、滞留の発生により局
部的に硬化反応が進行し長時間安定して成形し得る良好
な表面光沢と形状精度を有するドラム状物等のフェノー
ル系樹脂組成物は、見出されていない.
〔発明が解決しようとする課題〕
本発明の目的は、このような事情を鑑みて発明されたも
のであって、連続押出成形出来る特定の滑剤を特定量用
いたフェノール系樹脂組成物を用いて容易かつ安価で、
浮き出しのない良好な表面光沢を有し、かつ形状精度、
硬度、機械的強度の優れたフェノール系樹脂ドラム基材
を提供することにある.
〔課題を解決するための手段]
本発明者らは、上記した課題の解決について種々検討を
重ねた結果、フェノール系樹脂に、無機系充填材および
/または、有機系充填材、滑剤として脂肪酸アマイド系
滑剤および、必要に応じて配合するその他の添加剤を配
合したフェノール系樹脂組成物を用いると、浮き出しの
ない良好な表面光沢と形状精度、硬度、機械的強度に優
れたフェノール系樹脂ドラム基材が連続押出成形出来る
ことを見出し本発明に至った.
即ち、本発明は、フェノール系樹脂に、無機系充填剤、
および/または有機系充填剤、ならびに必要に応じて各
種の添加剤を、所望量配合してなるフェノール系樹脂組
成物を用いて押出成形される、フェノール系樹脂ドラム
基材において、該フェノール系樹脂組成物に、フェノー
ル系樹脂100重量部に対し、滑剤として、融点90〜
120℃である脂肪酸アマイド系滑剤を0.05〜5重
量部添加されてなる、フェノール系樹脂組成物を用いる
ことを特徴とするフェノール系樹脂ドラム基材である.
本発明に使用するフェノール系樹脂は、フェノール、ク
レゾール、キシレノール、レゾルシノール等のフェノー
ル類と、ホルムアルデヒド水溶液、バラホルムアルデヒ
ド、トリオキサン等のホルムアルデヒド類とを酸性触媒
を用いて反応させて得られるノボラック型フェノール樹
脂または、アルカリ性触媒を用いて反応させて得られる
レゾール型フェノー−ル樹脂或いは、ノボラック型フェ
ノール樹脂とレゾール型フェノール樹脂とを併用するこ
とも出来る.
上記フェノール系樹脂に添加する硬化剤としては、通常
へキサメチレンテトラミンが使用される。However, in plunger extrusion molding equipment, the extrusion pressure in the mold section is high, and intermittent extrusion is used, so it is difficult to obtain uniform molded products with good surface gloss and shape accuracy, and productivity is low. Under these circumstances, a molding method using a so-called screw-type extrusion molding device has been developed. This is a device that guides the phenolic resin composition kneaded and melted in an extruder into a mold through an adapter and shapes it into the final shape. However, with conventional phenolic resin compositions, the extrusion pressure in the mold part is high, and the flow path of the composition is difficult. It changes to A phenolic resin composition for drum-shaped objects with surface gloss and shape precision has not been found. [Problems to be Solved by the Invention] The purpose of the present invention was to solve the above problems by using a phenolic resin composition containing a specific amount of a specific lubricant that can be continuously extruded. easy and cheap,
Good surface gloss with no embossment, shape accuracy,
Our objective is to provide a phenolic resin drum base material with excellent hardness and mechanical strength. [Means for Solving the Problems] As a result of various studies to solve the above-mentioned problems, the inventors of the present invention have added phenolic resins, inorganic fillers and/or organic fillers, and fatty acid amide as a lubricant. By using a phenolic resin composition containing a lubricant and other additives as necessary, a phenolic resin drum base with good surface gloss without embossment, excellent shape accuracy, hardness, and mechanical strength can be obtained. We discovered that the material could be continuously extruded, leading to the present invention. That is, the present invention includes a phenolic resin, an inorganic filler,
In a phenolic resin drum base material that is extrusion-molded using a phenolic resin composition containing a desired amount of an organic filler and/or various additives as necessary, the phenolic resin In the composition, a lubricant with a melting point of 90 to 100 parts by weight of a phenolic resin is added.
This is a phenolic resin drum base material characterized by using a phenolic resin composition containing 0.05 to 5 parts by weight of a fatty acid amide lubricant having a temperature of 120°C.
The phenolic resin used in the present invention is a novolac type phenolic resin obtained by reacting phenols such as phenol, cresol, xylenol, and resorcinol with formaldehydes such as an aqueous formaldehyde solution, paraformaldehyde, and trioxane using an acidic catalyst. Alternatively, a resol type phenol resin obtained by reaction using an alkaline catalyst or a novolac type phenol resin and a resol type phenol resin can be used in combination. Hexamethylenetetramine is usually used as a curing agent added to the phenolic resin.
この場合、ヘキサメチレンテトラミンはノボラック型フ
ェノール樹脂100重量部に対し5重量部以上25重量
部未満の範囲で通常使用され、好ましくは、5〜20重
量部の範囲で使用される.この値が5重量部未満では、
満足な成形品を得ることが困難となり、また25重量部
以上では、形状精度の良い成形品を得ることが難しくな
る傾向にある.レゾール型フェノール樹脂を単独または
併用して用いる場合は、硬化剤を添加する必要はない.
本発明に用いる滑剤は、融点90〜120℃である脂肪
酸アマイド系滑剤である.例えばステアリン酸アマイド
、パルミチン酸アマイド、アラキン酸アマイド、ベヘン
酸アマイド、セロチン酸アマイド、モンタン酸アマイト
′等が挙げられる.滑剤の融点が90℃未満では、押出
成形時における滑剤の溶融が早く生じ、滑剤としての効
果が少なくなる.融点が120℃を越えると、押出成形
時の滑剤の溶融が遅くなり、滑剤の滑性効果が薄れると
同時に、フェノール系樹脂ドラム基材の表面に浮き出す
現象が生じ、該ドラム基材の表面光沢が庚なわれ、感光
体を塗布する場合、この浮き出した滑剤を除去するため
に溶剤等で洗浄する工程が増えるという欠点がある.
滑剤の配合量は、フェノール系樹脂100重景部に対し
0,05〜5重量部、好ましくは0.1〜2重量部であ
る, 0.05重量部未満では、滑性効果が少なく、形
状精度の良いフェノール系樹脂ドラム基材が得られない
。一方、5重量部を越えて使用すると、滑性効果が太き
《押出し成形性が悪くなり、フェノール系樹脂ドラム基
材の表面に滑剤が浮き出す欠点がある.
その他の添加剤としては、無機系充填剤、存機系充填剤
、着色剤、可塑剤、H燃剤等があり、次のものが挙げら
れる.
無機系充填剤としては、特に制限されるものではないが
、カーボンブラック、マグネシア、塩基性ケイ酸マグネ
シウム、炭酸マグネシウム、水酸化アルミニウム、水酸
化マグネシウム、アルミナ粉、各種ケイ酸塩、炭酸カル
シウム、ケイソウ土粉、カオリン、セライト、酸性白土
等の粉末無機物、セラミック繊維、ガラス繊維、アスベ
スト、ヘフドマン繊維、ロックウール、カーボンファイ
バー等の無機繊維等を用いることが出来る。In this case, hexamethylenetetramine is usually used in an amount of 5 parts by weight or more and less than 25 parts by weight, preferably in a range of 5 to 20 parts by weight, based on 100 parts by weight of the novolac type phenolic resin. If this value is less than 5 parts by weight,
It becomes difficult to obtain a satisfactory molded product, and if the amount exceeds 25 parts by weight, it tends to become difficult to obtain a molded product with good shape accuracy. When using resol type phenolic resin alone or in combination, there is no need to add a curing agent.
The lubricant used in the present invention is a fatty acid amide lubricant having a melting point of 90 to 120°C. Examples include stearic acid amide, palmitic acid amide, arachic acid amide, behenic acid amide, cerotic acid amide, and montanic acid amide'. If the melting point of the lubricant is less than 90°C, the lubricant will melt quickly during extrusion molding, reducing its effectiveness as a lubricant. If the melting point exceeds 120°C, the melting of the lubricant during extrusion molding will be delayed, the lubricating effect of the lubricant will be weakened, and at the same time, a phenomenon will occur where the lubricant will stand out on the surface of the phenolic resin drum base material, causing the surface of the drum base material to deteriorate. When coating a photoreceptor, the gloss is reduced, and the disadvantage is that cleaning with a solvent or the like is required to remove the lubricant that has embossed. The blending amount of the lubricant is 0.05 to 5 parts by weight, preferably 0.1 to 2 parts by weight, per 100 parts by weight of the phenolic resin. If it is less than 0.05 parts by weight, the lubricating effect will be small and the shape will deteriorate. It is not possible to obtain a highly accurate phenolic resin drum base material. On the other hand, if it is used in an amount exceeding 5 parts by weight, the lubricating effect will be too strong (extrusion moldability will be poor, and the lubricant will stand out on the surface of the phenolic resin drum base material). Other additives include inorganic fillers, organic fillers, colorants, plasticizers, and H refueling agents, including the following: Inorganic fillers include, but are not limited to, carbon black, magnesia, basic magnesium silicate, magnesium carbonate, aluminum hydroxide, magnesium hydroxide, alumina powder, various silicates, calcium carbonate, and diatom. Powdered inorganic materials such as earth powder, kaolin, celite, and acid clay, and inorganic fibers such as ceramic fibers, glass fibers, asbestos, Hefdman fibers, rock wool, and carbon fibers can be used.
有機系充填剤としては、特に制限されるものではないが
、祇バルブ、木粉、木綿、リンター、ポリイミド繊維、
ビニロン繊維、芳香族ボリアミド繊維、芳香族ポリエス
テル繊維等の有v9繊維等の繊維状或いは、織布、不織
布等である.充填剤の使用量は、フェノール系樹脂10
0重量部に対して、通常、25〜200重量部、好まし
くは40〜180重量部である.25重量部未満である
と充分な強度が得られず、一方、200重量部を越える
場合は押出成形性が悪くなる.
着色剤としては、スピリットブラック、モリブデン赤、
フタロシアンブルー、フタ口シアングリーン、ハンザイ
エロー等を用いることが出来る.可塑剤としては、フル
フラール、アルキルフェノール、トリクレジルホスフェ
ート、ポリエチレングリコール、ジブチルフタレート、
P−}ルエンスルホアミド等の一最に使用されているも
のが有効である.
難燃剤としては、酸化アンチモン、トリス(2,3−ジ
ブロモブ口ピル)ホスフエート等が挙げられる.
本発明のフェノール系樹脂ドラム基材を得る方法は、上
記ノボラック型フェノール樹脂、硬化剤としてヘキサメ
チレンテトラミン、またはレゾール型フェノール樹脂に
無機系充填材、および/または、有機系充填材、滑剤と
して融点90〜120℃である脂肪酸アマイド系滑剤、
その他に必要に応じて、着色剤、可塑剤、難燃剤等を添
加し混練、粉砕してフェノール系樹脂組成物が得られる
.混練、粉砕は、公知の方法で総て実施し得る。Examples of organic fillers include, but are not particularly limited to, gibber, wood flour, cotton, linters, polyimide fibers,
They are fibrous materials such as V9 fibers such as vinylon fibers, aromatic polyamide fibers, and aromatic polyester fibers, woven fabrics, and non-woven fabrics. The amount of filler used is phenolic resin 10
The amount is usually 25 to 200 parts by weight, preferably 40 to 180 parts by weight. If it is less than 25 parts by weight, sufficient strength will not be obtained, while if it exceeds 200 parts by weight, extrusion moldability will deteriorate. Colorants include spirit black, molybdenum red,
Phthalocyan blue, cyan green, Hansa yellow, etc. can be used. Plasticizers include furfural, alkylphenol, tricresyl phosphate, polyethylene glycol, dibutyl phthalate,
The most commonly used compounds, such as P-}luenesulfamide, are effective. Examples of flame retardants include antimony oxide, tris(2,3-dibromobutyl) phosphate, and the like. The method for obtaining the phenolic resin drum base material of the present invention includes adding the above novolac type phenol resin, hexamethylenetetramine as a curing agent, or resol type phenol resin with an inorganic filler and/or an organic filler, and a melting point as a lubricant. fatty acid amide lubricant having a temperature of 90 to 120°C;
In addition, colorants, plasticizers, flame retardants, etc. are added as necessary, and a phenolic resin composition is obtained by kneading and pulverizing. Kneading and pulverization can be carried out by any known method.
即ち、混練は熱ロール、コニーダ等、粉砕はスピードミ
ル、バワーミル等が使用出来る.得られたフェノール系
樹脂組成物を、圧縮成形、トランスファー成形、押出成
形等により樹脂ドラム基材が成形される.上記成形方法
のうち特に押出成形に適用した場合効果が大きい.
〔実施例]
以下、実施桝により本発明を説明する.実施例1〜6.
比較例1〜3
ノボラック型フェノール樹脂(三井東圧化学■製120
00 、軟化点96℃)にヘキサメチレンテ[・ラミン
、無機系充填材、および/または有機系充填材、脂肪酸
アマイド系滑剤、および、その他の添加剤を第1表に示
す配合割合で混合し、混合物を前ロール95〜100℃
、後ロール55〜60℃の温度条件で6分間ロール混練
した後、バワーミル(4ffiIl1スクリーン使用)
にて粉砕、整粒して樹脂組成物を得た.得られた樹脂組
成物について下記押出試験を実施して、樹脂ドラム基材
を成形し、物性を測定した.結果を第1表に示す.
実施例7〜9,比較例4〜5。That is, a hot roll, co-kneader, etc. can be used for kneading, and a speed mill, bower mill, etc. can be used for grinding. The resulting phenolic resin composition is molded into a resin drum base material by compression molding, transfer molding, extrusion molding, etc. Among the above molding methods, it is especially effective when applied to extrusion molding. [Example] The present invention will be explained below with reference to examples. Examples 1-6.
Comparative Examples 1 to 3 Novolac type phenolic resin (120 manufactured by Mitsui Toatsu Chemical Co., Ltd.)
00, softening point 96°C), hexamethylenete[lamin, an inorganic filler and/or an organic filler, a fatty acid amide lubricant, and other additives were mixed in the proportions shown in Table 1. , pre-roll the mixture at 95-100℃
After kneading with the rear roll for 6 minutes at a temperature of 55 to 60°C, a bower mill (using 4ffil1 screen)
The resin composition was pulverized and sized to obtain a resin composition. The obtained resin composition was subjected to the following extrusion test to form a resin drum base material and its physical properties were measured. The results are shown in Table 1. Examples 7-9, Comparative Examples 4-5.
レゾール型フェノール樹脂(昭和高分子製、IBRP)
に無機系充填材、および/または有機系充填材、脂肪酸
アマイド系滑剤、および、その他の添加剤を第1表に示
す配合割合で混合し、実施例1と同じ条件により混練、
粉砕、整粒して、樹脂組成物を得た.得られた樹脂組成
物について下記押出試験を実施して、樹脂ドラム基材を
成形し、物性を測定した。結果を第1表に示す.
押出成形試験
口径30a+m、L/D・22の押出機により、スクリ
ュー低部の径が26ms計量部に続く先端部に径26m
+m、長さ90l(3D)の平滑部を有する圧縮比2.
0のスクリューを川い、各成形材料を使用し、径30m
m、肉K 2 amのドラム基材を成形した.押出成形
の条件は、ホッパ一下より2Dは室温、続いて3〜10
0は60℃,110〜140は80″C,150〜18
0は105℃、190〜220は150 ’Cに設定し
、スクリュー回転数35rpmの条件で押出成形を実施
した.
物性試験
1.成形物の浮き出し性
スクリュー型押出機で成形されたフェノール系樹脂ドラ
ム基材を定尺に切断した。滑剤の浮き出し状況を、目視
にて観察し評価した.
判定方法
◎:良好、Δ:やや浮き出し、×:浮き出し有2.感光
体の塗布性
スクリュー型押出機で成形されたフェノール系樹脂ドラ
ム基材を定尺に切断した.このドラムを使用し、感光体
を塗布した.感光体の塗布状況を観察し、評価した.
判定方法
◎:良好、Δ:やや劣る、×:不良
〔発明の効果〕
本発明のフェノール系樹脂ドラム基材は上記のように、
フェノール系樹脂に、無機充填剤および/または、有機
系充填剤、ならびに必要に応じて各種の添加剤を、所望
量配合してなるフェノール系樹脂組成物において、特定
の滑剤を特定量配合することにより、浮き出しのない、
表面光沢の良いフェノール系樹脂ドラム基材が、連続し
て得られる効果を存しており、産業界に寄与すること大
である。Resol type phenolic resin (Showa Kobunshi, IBRP)
An inorganic filler and/or an organic filler, a fatty acid amide lubricant, and other additives were mixed in the proportions shown in Table 1, and the mixture was kneaded under the same conditions as in Example 1.
A resin composition was obtained by crushing and sizing. The obtained resin composition was subjected to the following extrusion test to form a resin drum base material and its physical properties were measured. The results are shown in Table 1. Extrusion molding test Using an extruder with a diameter of 30a+m and L/D・22, the diameter of the lower part of the screw was 26ms, and the diameter of the tip following the measuring part was 26m.
+ m, compression ratio 2. with smooth section of length 90 l (3D).
0 screw, using each molding material, diameter 30m
A drum base material of K 2 am and K 2 am was molded. The conditions for extrusion molding are room temperature for 2D from the bottom of the hopper, then 3 to 10
0 is 60℃, 110~140 is 80''C, 150~18
Extrusion molding was carried out under conditions such as 0 was set at 105°C, 190 to 220 was set at 150'C, and the screw rotation speed was 35 rpm. Physical property test 1. Embossability of molded product A phenolic resin drum base material molded using a screw extruder was cut into regular lengths. The appearance of the lubricant was visually observed and evaluated. Judgment method: ◎: good, Δ: slightly raised, ×: raised 2. Coating of photoreceptor A phenolic resin drum base material molded using a screw-type extruder was cut into regular lengths. This drum was used to coat the photoreceptor. The coating status of the photoreceptor was observed and evaluated. Judgment method: ◎: Good, Δ: Slightly poor, ×: Poor [Effects of the invention] As described above, the phenolic resin drum base material of the present invention
Blending a specific amount of a specific lubricant in a phenolic resin composition formed by blending a desired amount of an inorganic filler and/or an organic filler and various additives as necessary with a phenolic resin. Due to this, there is no embossment,
The phenolic resin drum base material with good surface gloss has a continuous effect and will greatly contribute to the industrial world.
特許出願人 三井東圧化学株式会社手続{甫正書(
方式)
平成1年6月12日
特許庁長官 吉 田 文 毅 殿
1.事件の表示
平成01年特許願第52058号
2.発明の名称
?エノール系樹脂ドラム基材
3.補正をする者
事件との関係 特許出願人
住所 東京都千代田区霞が関三丁目2番5号4.補正命
令の日付
平成1年5月30日(発送)
5.補正の対象
明細書
6,補正の内容Patent applicant: Mitsui Toatsu Chemical Co., Ltd.
Format) June 12, 1999 Fumi Takeshi Yoshida, Commissioner of the Japan Patent Office 1. Case Description 1999 Patent Application No. 52058 2. The name of the invention? Enol-based resin drum base material 3. Relationship with the case of the person making the amendment Patent applicant address: 3-2-5 Kasumigaseki, Chiyoda-ku, Tokyo 4. Date of amendment order: May 30, 1999 (shipped) 5. Specification to be amended 6, Contents of amendment
Claims (1)
機系充填剤、ならびに必要に応じて各種の添加剤を、所
望量配合してなるフェノール系樹脂組成物を用いて、押
出成形される、フェノール系樹脂ドラム基材において、
該フェノール系樹脂組成物に、フェノール系樹脂100
重量部に対し、滑剤として、融点90〜120℃である
脂肪酸アマイド系滑剤を0.05〜5重量部添加されて
なる、フェノール系樹脂組成物を用いることを特徴とす
るフェノール系樹脂ドラム基材。Phenol is extrusion molded using a phenol resin composition made by blending a phenol resin with a desired amount of an inorganic filler, an organic filler, and various additives as necessary. In the resin drum base material,
The phenolic resin composition contains 100% of the phenolic resin.
A phenolic resin drum base material characterized by using a phenolic resin composition in which 0.05 to 5 parts by weight of a fatty acid amide lubricant having a melting point of 90 to 120°C is added as a lubricant based on the weight part. .
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP5205889A JPH02232252A (en) | 1989-03-06 | 1989-03-06 | Phenol resin drum base material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP5205889A JPH02232252A (en) | 1989-03-06 | 1989-03-06 | Phenol resin drum base material |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH02232252A true JPH02232252A (en) | 1990-09-14 |
Family
ID=12904214
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP5205889A Pending JPH02232252A (en) | 1989-03-06 | 1989-03-06 | Phenol resin drum base material |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH02232252A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5563190A (en) * | 1994-08-04 | 1996-10-08 | Sumitomo Bakelite Company Limited | Phenolic resin molding material |
-
1989
- 1989-03-06 JP JP5205889A patent/JPH02232252A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5563190A (en) * | 1994-08-04 | 1996-10-08 | Sumitomo Bakelite Company Limited | Phenolic resin molding material |
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