JP3362969B2 - Charging device - Google Patents
Charging deviceInfo
- Publication number
- JP3362969B2 JP3362969B2 JP18208894A JP18208894A JP3362969B2 JP 3362969 B2 JP3362969 B2 JP 3362969B2 JP 18208894 A JP18208894 A JP 18208894A JP 18208894 A JP18208894 A JP 18208894A JP 3362969 B2 JP3362969 B2 JP 3362969B2
- Authority
- JP
- Japan
- Prior art keywords
- weight
- parts
- charging roller
- hardness
- charging
- 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 - Lifetime
Links
- 238000000034 method Methods 0.000 claims description 15
- 229920000642 polymer Polymers 0.000 claims description 15
- 229920005862 polyol Polymers 0.000 claims description 15
- 150000003077 polyols Chemical class 0.000 claims description 15
- 239000000463 material Substances 0.000 claims description 5
- 229920005830 Polyurethane Foam Polymers 0.000 claims description 4
- 239000011496 polyurethane foam Substances 0.000 claims description 4
- 241000628997 Flos Species 0.000 claims description 2
- 229920001940 conductive polymer Polymers 0.000 claims 1
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 12
- 229910052751 metal Inorganic materials 0.000 description 12
- 239000002184 metal Substances 0.000 description 12
- 239000006260 foam Substances 0.000 description 11
- 239000007787 solid Substances 0.000 description 10
- 239000000126 substance Substances 0.000 description 9
- 239000004721 Polyphenylene oxide Substances 0.000 description 8
- 239000002245 particle Substances 0.000 description 8
- 229920000570 polyether Polymers 0.000 description 8
- ZPFAVCIQZKRBGF-UHFFFAOYSA-N 1,3,2-dioxathiolane 2,2-dioxide Chemical compound O=S1(=O)OCCO1 ZPFAVCIQZKRBGF-UHFFFAOYSA-N 0.000 description 7
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 6
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 6
- 125000001931 aliphatic group Chemical group 0.000 description 6
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 6
- 235000011187 glycerol Nutrition 0.000 description 6
- 238000002156 mixing Methods 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- DAZXVJBJRMWXJP-UHFFFAOYSA-N n,n-dimethylethylamine Chemical compound CCN(C)C DAZXVJBJRMWXJP-UHFFFAOYSA-N 0.000 description 6
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 6
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 5
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 5
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 5
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 5
- 239000006229 carbon black Substances 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 5
- 239000012975 dibutyltin dilaurate Substances 0.000 description 5
- 229920001296 polysiloxane Polymers 0.000 description 5
- 238000009864 tensile test Methods 0.000 description 5
- 239000004925 Acrylic resin Substances 0.000 description 4
- 229920000178 Acrylic resin Polymers 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- 229910044991 metal oxide Inorganic materials 0.000 description 4
- 150000004706 metal oxides Chemical class 0.000 description 4
- 239000004094 surface-active agent Substances 0.000 description 4
- 239000004677 Nylon Substances 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 239000011247 coating layer Substances 0.000 description 3
- 239000006258 conductive agent Substances 0.000 description 3
- 229920001778 nylon Polymers 0.000 description 3
- 239000012779 reinforcing material Substances 0.000 description 3
- HZNVUJQVZSTENZ-UHFFFAOYSA-N 2,3-dichloro-5,6-dicyano-1,4-benzoquinone Chemical compound ClC1=C(Cl)C(=O)C(C#N)=C(C#N)C1=O HZNVUJQVZSTENZ-UHFFFAOYSA-N 0.000 description 2
- VBIIFPGSPJYLRR-UHFFFAOYSA-M Stearyltrimethylammonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)C VBIIFPGSPJYLRR-UHFFFAOYSA-M 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 description 2
- 239000003093 cationic surfactant Substances 0.000 description 2
- 239000013013 elastic material Substances 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- 239000000806 elastomer Substances 0.000 description 2
- 238000005187 foaming Methods 0.000 description 2
- 229940094506 lauryl betaine Drugs 0.000 description 2
- MHCFAGZWMAWTNR-UHFFFAOYSA-M lithium perchlorate Chemical compound [Li+].[O-]Cl(=O)(=O)=O MHCFAGZWMAWTNR-UHFFFAOYSA-M 0.000 description 2
- 229910001486 lithium perchlorate Inorganic materials 0.000 description 2
- DVEKCXOJTLDBFE-UHFFFAOYSA-N n-dodecyl-n,n-dimethylglycinate Chemical compound CCCCCCCCCCCC[N+](C)(C)CC([O-])=O DVEKCXOJTLDBFE-UHFFFAOYSA-N 0.000 description 2
- 239000004014 plasticizer Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- ULWHHBHJGPPBCO-UHFFFAOYSA-N propane-1,1-diol Chemical compound CCC(O)O ULWHHBHJGPPBCO-UHFFFAOYSA-N 0.000 description 2
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 2
- BAZAXWOYCMUHIX-UHFFFAOYSA-M sodium perchlorate Chemical compound [Na+].[O-]Cl(=O)(=O)=O BAZAXWOYCMUHIX-UHFFFAOYSA-M 0.000 description 2
- 229910001488 sodium perchlorate Inorganic materials 0.000 description 2
- FPGGTKZVZWFYPV-UHFFFAOYSA-M tetrabutylammonium fluoride Chemical compound [F-].CCCC[N+](CCCC)(CCCC)CCCC FPGGTKZVZWFYPV-UHFFFAOYSA-M 0.000 description 2
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 2
- 229910001887 tin oxide Inorganic materials 0.000 description 2
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 2
- IMNIMPAHZVJRPE-UHFFFAOYSA-N triethylenediamine Chemical compound C1CN2CCN1CC2 IMNIMPAHZVJRPE-UHFFFAOYSA-N 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- -1 whiskers Substances 0.000 description 2
- AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 description 1
- WHQOKFZWSDOTQP-UHFFFAOYSA-N 2,3-dihydroxypropyl 4-aminobenzoate Chemical compound NC1=CC=C(C(=O)OCC(O)CO)C=C1 WHQOKFZWSDOTQP-UHFFFAOYSA-N 0.000 description 1
- HVYJSOSGTDINLW-UHFFFAOYSA-N 2-[dimethyl(octadecyl)azaniumyl]acetate Chemical compound CCCCCCCCCCCCCCCCCC[N+](C)(C)CC([O-])=O HVYJSOSGTDINLW-UHFFFAOYSA-N 0.000 description 1
- 239000004970 Chain extender Substances 0.000 description 1
- 239000005058 Isophorone diisocyanate Substances 0.000 description 1
- JHWNWJKBPDFINM-UHFFFAOYSA-N Laurolactam Chemical compound O=C1CCCCCCCCCCCN1 JHWNWJKBPDFINM-UHFFFAOYSA-N 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- 229920000299 Nylon 12 Polymers 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 1
- 150000004056 anthraquinones Chemical class 0.000 description 1
- HIFVAOIJYDXIJG-UHFFFAOYSA-N benzylbenzene;isocyanic acid Chemical class N=C=O.N=C=O.C=1C=CC=CC=1CC1=CC=CC=C1 HIFVAOIJYDXIJG-UHFFFAOYSA-N 0.000 description 1
- WOWHHFRSBJGXCM-UHFFFAOYSA-M cetyltrimethylammonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[N+](C)(C)C WOWHHFRSBJGXCM-UHFFFAOYSA-M 0.000 description 1
- KYKAJFCTULSVSH-UHFFFAOYSA-N chloro(fluoro)methane Chemical compound F[C]Cl KYKAJFCTULSVSH-UHFFFAOYSA-N 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- TWFQJFPTTMIETC-UHFFFAOYSA-N dodecan-1-amine;hydron;chloride Chemical compound [Cl-].CCCCCCCCCCCC[NH3+] TWFQJFPTTMIETC-UHFFFAOYSA-N 0.000 description 1
- DDXLVDQZPFLQMZ-UHFFFAOYSA-M dodecyl(trimethyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCC[N+](C)(C)C DDXLVDQZPFLQMZ-UHFFFAOYSA-M 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- KTWOOEGAPBSYNW-UHFFFAOYSA-N ferrocene Chemical compound [Fe+2].C=1C=C[CH-]C=1.C=1C=C[CH-]C=1 KTWOOEGAPBSYNW-UHFFFAOYSA-N 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000004088 foaming agent Substances 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000010907 mechanical stirring Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- FUIRUFXAVIHAQB-UHFFFAOYSA-N n,n,2,2-tetramethylpropan-1-amine Chemical compound CN(C)CC(C)(C)C FUIRUFXAVIHAQB-UHFFFAOYSA-N 0.000 description 1
- 108091008695 photoreceptors Proteins 0.000 description 1
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 1
- 238000007517 polishing process Methods 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920005906 polyester polyol Polymers 0.000 description 1
- 229920001195 polyisoprene Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 230000002787 reinforcement Effects 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- DZLFLBLQUQXARW-UHFFFAOYSA-N tetrabutylammonium Chemical compound CCCC[N+](CCCC)(CCCC)CCCC DZLFLBLQUQXARW-UHFFFAOYSA-N 0.000 description 1
- KBLZDCFTQSIIOH-UHFFFAOYSA-M tetrabutylazanium;perchlorate Chemical compound [O-]Cl(=O)(=O)=O.CCCC[N+](CCCC)(CCCC)CCCC KBLZDCFTQSIIOH-UHFFFAOYSA-M 0.000 description 1
- UGNWTBMOAKPKBL-UHFFFAOYSA-N tetrachloro-1,4-benzoquinone Chemical compound ClC1=C(Cl)C(=O)C(Cl)=C(Cl)C1=O UGNWTBMOAKPKBL-UHFFFAOYSA-N 0.000 description 1
- NLDYACGHTUPAQU-UHFFFAOYSA-N tetracyanoethylene Chemical group N#CC(C#N)=C(C#N)C#N NLDYACGHTUPAQU-UHFFFAOYSA-N 0.000 description 1
- PCCVSPMFGIFTHU-UHFFFAOYSA-N tetracyanoquinodimethane Chemical compound N#CC(C#N)=C1C=CC(=C(C#N)C#N)C=C1 PCCVSPMFGIFTHU-UHFFFAOYSA-N 0.000 description 1
- WGHUNMFFLAMBJD-UHFFFAOYSA-M tetraethylazanium;perchlorate Chemical compound [O-]Cl(=O)(=O)=O.CC[N+](CC)(CC)CC WGHUNMFFLAMBJD-UHFFFAOYSA-M 0.000 description 1
- FHCPAXDKURNIOZ-UHFFFAOYSA-N tetrathiafulvalene Chemical compound S1C=CSC1=C1SC=CS1 FHCPAXDKURNIOZ-UHFFFAOYSA-N 0.000 description 1
- 239000002888 zwitterionic surfactant Substances 0.000 description 1
Landscapes
- Electrostatic Charge, Transfer And Separation In Electrography (AREA)
- Rolls And Other Rotary Bodies (AREA)
Description
【発明の詳細な説明】
【0001】
【産業上の利用分野】本発明は、電子写真プロセスで使
用される半導電性高分子部材を用いた画像形成装置等の
帯電装置に関する。
【0002】
【従来の技術】近年、電子技術の進歩に伴い、電子写真
プロセスで利用する半導電性部材に対する要求も高まっ
ており、とりわけ帯電プロセスに利用される弾性ローラ
が注目されている。このような用途に用いられる半導電
性部材は所定の電気抵抗値、硬度であるのみならず、連
続して圧力を加えながら回転する等の応力に対し充分な
機械的強度を保持することが必要である。
【0003】従来、このような用途に用いられる半導電
性部材は、高分子エラストマーや高分子フォーム等の高
分子物質に金属酸化物の粉末、カーボンブラック、過塩
素酸リチウムや過塩素酸ナトリウムの如き無機イオン物
質、変性脂肪族・ジメチルエチルアンモニウムエトサル
フェート等の如き陽イオン性界面活性剤、ほうふっ化テ
トラブチルアンモニウム等の第4級アンモニウム塩の如
き有機イオン物質、電荷移動錯体を形成し得る電子受容
物質等の導電剤を混入することにより、所定の抵抗値に
調整した高分子部材が用いられている。
【0004】
【発明が解決しようとする課題】このような部材は高品
位画像を得るために低硬度である必要がある。高分子部
材を低硬度化するためには、気泡を混入しフォーム体と
する方法、補強材として用いられるカーボンブラック等
の配合量を低下させたり、補強度の低いグレードに変更
する方法、オイル等の可塑剤を添加する方法が用いられ
ている。ところがフォーム体とする方法や補強材を減量
したり、補強材の種類を変更するだけでは部材の破断強
度が低下し、この種の部材は通常500g以上の荷重を
かけた状態で回転させて使用されるため、破断強度が
2.2kgf/cm2 を下回ると長期間の使用中に部材
が破損することがあり、特に2kgf/cm2 以下で部
材の破損頻度が増大するという問題点があった。また、
可塑剤を添加する方法では長期間の使用中に可塑剤がブ
リードし、感光体を汚染するという問題点があった。従
って、本発明はかかる従来の半導電性高分子部材の欠点
を解決し、上述した諸特性を兼備した半導電性高分子部
材を用いた画像形成装置の帯電装置を提供することを目
的とする。
【0005】
【問題を解決するための手段】本発明者等は、上記目的
を達成するため鋭意検討を重ねた結果、ポリウレタンフ
ォームの製造方法を特殊な方法とし、これに導電剤を添
加して導電性を付与することにより、破断強度が2kg
f/cm2 以上であり、アスカーC硬度が50°以下で
あり、かつ電気抵抗が1×104 〜1×1012Ωcmで
ある半導電性高分子部材が初めて得られることを知見
し、本発明をなすに至った。
【0006】以下、本発明につき詳しく説明する。本発
明に係わる半導電性高分子部材は、ポリウレタンフォー
ムに導電性付与剤を添加混合してなるものであり、その
電気抵抗が温度22℃、相対湿度55%において、測定
電圧1000Vで体積抵抗1×104 〜1×1012Ωc
m、好ましくは2×107 〜5×1011Ωcmであり、
破断強度が2kgf/cm2 以上、好ましくは2.2k
gf/cm2 以上であり、アスカーC硬度が50°以
下、好ましくは42°以下であるものである。
【0007】ここで、ポリウレタンフォームは、ポリエ
ーテルポリオール、ポリエステルポリオール、ポリブタ
ジエンポリオール、ポリイソプレンポリオール、グリセ
リンにポリエチレンオキサイドやポリプロピレンオキサ
イドを付加重合したポリオール、エチレングリコール、
プロパンジオール、ブタンジオール等のポリオール成分
を、トリレンジイソシアネート(TDI)、ジフェニル
メタンジイソシアネート(MDI)、粗製ジフェニルメ
タンジイソシアネート(クルードMDI)やウレトンイ
ミン変性ジフェニルメタンジイソシアネート等の液状M
DI、イソホロンジイソシアネート等のイソシアネート
によりプレポリマー化した材料を構成材料として含むこ
とにより本発明の目的が効果的に達成される。
【0008】鎖延長剤には、エチレングリコール、プロ
パンジオール、ブタンジオール等公知のポリオールを用
いることができるが、特に分子量500以下、好ましく
は分子量200以下のポリオールが好ましく用いられ
る。また、発泡方法はメカニカルフロス法(機械的な攪
拌により気泡を混入する方法)とすることにより、本発
明の目的が効果的に達成される。
【0009】本発明の半導電性高分子部材は、上記高分
子物質を基材とし、これに導電性付与剤を添加するもの
である。導電性を付与するための導電剤に制限はない
が、金属や金属酸化物の粉末やウイスカー、カーボンブ
ラック等のフィラー、過塩素酸リチウム、過塩素酸ナト
リウム、過塩素酸カルシウムの如き無機イオン物質及び
/またはラウリルトリメチルアンモニウムクロライド、
ステアリルトリメチルアンモニウムクロライド、オクタ
デシルトリメチルアンモニウムクロライド、ドデシルル
アンモニウムクロライド、ヘキサデシルトリメチルアン
モニウムクロライド、変性脂肪族・ジメチルエチルアン
モニウムエトサルフェートの如き陽イオン性界面活性
剤、ラウリルベタイン、ステアリルベタイン、ジメチル
アルキルラウリルベタインの如き両性イオン界面活性
剤、過塩素酸テトラエチルアンモニウム、過塩素酸テト
ラブチルアンモニウム、ほうふっ化テトラブチルアンモ
ニウム等の4級アンモニウム塩の如き有機イオン物質及
び/又は親水性のポリオールやポリエステルの如き帯電
防止剤、テトラシアノエチレン、テトラシアノキノジメ
タン、ベンゾキノン、クロルアニル、アントラキノン、
アントラセン、ジクロロジシアノベンゾキノン、フェロ
セン、フタロシアニン等の電荷移動錯体を形成し得る電
子受容物質等が用いることが出来、また基材であるウレ
タンフォームとの相溶性を向上させる等の目的でこれら
の化合物の誘導体や電荷移動錯体を形成し得る電子受容
物質をテトラチアフルバレン、リチウム等の電子供与物
質と錯体を形成した形で使用してもよい。なお、本発明
の効果を損なわない範囲で、プレポリマー化していない
ポリマーポリオール等を併用したり、水やフロン等の発
泡剤を併用してもよい。
【0010】上記の部材を帯電装置に用いる形状に制限
はないが、通常芯金を中央に配設したローラ形状にして
用いられる。ローラ形状にする方法に制限はないが、通
常砥石により研磨する方法やローラ形状に合わせたモー
ルドを使用して自己スキン付きフォームやエラストマー
を得る方法が用いられる。
【0011】また、環境安全性、騒音、画像改善等の観
点から本発明の帯電部材の上に1つ以上の導電性、半導
電性、あるいは絶縁性の各種被膜層を設けることも可能
である。これらの各種被膜層としては、例えば、ナイロ
ン等が好ましく用いられ、特にナイロン12を15重量
%以上含有する共重合ナイロンで形成することにより、
帯電環境安全性を向上させることが可能である。この共
重合ナイロンの融点は、120℃以下が良く、特に70
〜120℃、とりわけ90〜110℃であることが好ま
しい。この場合の被膜の体積固有抵抗率に制限はない
が、通常106 〜1013Ωcmとすることが好ましい。
【0012】この体積抵抗率を調整する目的で、カーボ
ンブラック、酸化スズ、酸化チタン等の金属酸化物粒子
を一種以上配合することができる。また、アクリル樹脂
成分を5〜70重量%含有するウレタン変性アクリル樹
脂を含む樹脂層で被膜層を形成することも好ましく、ア
クリル樹脂成分のガラス転移温度が室温から120℃の
範囲のものが好ましく用いられる。この場合の被膜の体
積抵抗率に制限はないが、通常106 〜1013Ωcmと
することが好ましい。
【0013】この体積抵抗率を調整する目的で、カーボ
ンブラック、酸化スズ、酸化チタン等の金属酸化物粒子
を一種以上配合することができ、更にウレタン変性アク
リル樹脂中にシリコーン成分を1〜50重量%添加する
ことも好ましい。また、被帯電体との表面近傍に粒径3
5〜100μmの粒子を配置することにより騒音を低減
することができる。この場合の粒子に制限はなく、絶縁
性または導電性を有する粒子のいずれも好ましく用いら
れ、絶縁性粒子を導電性の塗膜または弾性体材料で被覆
してもよい。粒子の配合量に制限はないが、塗膜または
弾性体材料を形成し得るポリマー100重量部に対し3
〜50重量部が好ましい。
【0014】以下、実施例、比較例を示して本発明を具
体的に説明するが、本発明は下記実施例に制限されるも
のではない。なお、湿度は相対湿度、硬度はアスカーC
硬度である。
【実施例】
[実施例1]グリセリンにプロピレンオキサイドとエチ
レンオキサイドを付加して分子量5000としたポリエ
ーテルポリオールをトリレンジイソシアネートでプレポ
リマー化したポリエーテル系プレポリマー100重量
部、1,4ブタンジオール6.55重量部、シリコーン
系界面活性剤2重量部、ジブチルチンジラウレート0.
01重量部、変性脂肪族・ジメチルエチルアンモニウム
エトサルフェート0.015重量部をミキサーで混合・
機械発泡し、その混合物で直径6mmの金属製シャフト
を中心に配設した直径16.5mm,長さ215mmの
自己スキン付きウレタンフォーム帯電ローラを作成し
た。帯電ローラの硬度は38°であった。
【0015】次いで、上記帯電ローラを、図1に示す画
像形成装置に組み込み、温度、湿度が各々22℃、55
%の環境で抵抗値を測定したところ1000Vで1×1
08Ωであった。−1700Vの定電圧電源を帯電電源
として、グレースケール、黒ベタ、白ベタ画像を印刷さ
せたところ良好な画像が得られた。更に、この帯電ロー
ラの金属製シャフトを除去して厚さ4mmのリング状試
験片を作成し、引っ張り試験をしたところ破断強度は
2.9kgf/cm2 であった。
【0016】[比較例1]グリセリンにプロピレンオキ
サイドとエチレンオキサイドを付加して分子量5000
としたポリエーテルポリオール100重量部、トリレン
ジイソシアネート6.03重量部、シリコーン系界面活
性剤2重量部、ジブチルチンジラウレート0.03重量
部、変性脂肪族・ジメチルエチルアンモニウムエトサル
フェート0.015重量部をミキサーで混合・機械発泡
し、その混合物で直径6mmの金属製シャフトを中心に
配設した直径16.5mm、長さ215mmの自己スキ
ン付きウレタンフォーム帯電ローラを作成した。帯電ロ
ーラの硬度は35°であった。
【0017】次いで、上記帯電ローラを、第1図に示す
画像形成装置に組み込み、温度、湿度が各々22℃、5
5%の環境で抵抗値を測定したところ1000Vで、1
×108 Ωであった。−1700Vの定電圧電源を帯電
電源として、グレースケール、黒ベタ、白ベタ画像を印
刷したところ良好な画像が得られた。更に、この帯電ロ
ーラの金属製シャフトを除去して厚さ4mmのリング状
試験片を作成し、引っ張り試験を行ったところ破断強度
は0.6kgf/cm2 であった。
【0018】[比較例2]グリセリンにプロピレンオキ
サイドとエチレンオキサイドを付加して分子量5000
としたポリエーテルポリオール100重量部、粗製ジフ
ェニルメタンジイソシアネート9.15重量部、シリコ
ーン系界面活性剤2重量部、ジブチルチンジラウレート
0.003重量部、変性脂肪族・ジメチルエチルアンモ
ニウムエトサルフェート0.015重量部をミキサーで
混合・機械発泡し、その混合物で直径6mmの金属製シ
ャフトを中心に配設した直径16.5mm、長さ215
mmの自己スキン付きウレタンフォーム帯電ローラを作
成した。帯電ローラの硬度は38°であった。
【0019】次いで、上記帯電ローラを、第1図に示す
画像形成装置に組み込み、温度、湿度が各々22℃、5
5%の環境で抵抗値を測定したところ1000Vで、1
×108 Ωであった。−1700Vの定電圧電源を帯電
電源として、グレースケール、黒ベタ、白ベタ画像を印
刷したところ良好な画像が得られた。更に、この帯電ロ
ーラの金属製シャフトを除去して厚さ4mmのリング状
試験片を作成し、引っ張り試験を行ったところ破断強度
は0.2kgf/cm2 であった。
【0020】[比較例3]グリセリンにプロピレンオキ
サイドとエチレンオキサイドを付加して分子量5000
としたポリエーテルポリオールをトリレンジイソシアネ
ートでプレポリマー化したポリエーテル系プレポリマー
100重量部、1,4ブタンジオール6.1重量部、蒸
留水0.5重量部、ジブチルチンジラウレート0.01
重量部、トリエチレンジアミン0.03重量部、変性脂
肪族・ジメチルエチルアンモニウムエトサルフェート
0.015重量部をミキサーで混合し、その混合物で直
径6mmの金属製シャフトを中心に配設した直径16.
5mm,長さ215mmの自己スキン付きウレタンフォ
ーム帯電ローラを作成した。帯電ローラの硬度は37°
であった。
【0021】次いで、上記帯電ローラを、図1に示す画
像形成装置に組み込み、温度、湿度が各々22℃、55
%の環境で抵抗値を測定したところ1000Vで1×1
08Ωであった。−1700Vの定電圧電源を帯電電源
として、グレースケール、黒ベタ、白ベタ画像を印刷さ
せたところ良好な画像が得られた。更に、この帯電ロー
ラの金属製シャフトを除去して厚さ4mmのリング状試
験片を作成し、引っ張り試験をしたところ破断強度は
0.9kgf/cm2 であった。
【0022】[比較例4]グリセリンにプロピレンオキ
サイドとエチレンオキサイドを付加して分子量5000
としたポリエーテルポリオール100重量部、トリレン
ジイソシアネート15.5重量部、1,4−ブタンジオ
ール6.55重量部、シリコーン系界面活性剤2重量
部、ジブチルチンジラウレート0.01重量部、変性脂
肪族・ジメチルエチルアンモニウムエトサルフェート
0.015重量部をミキサーで混合・機械発泡し、その
混合物で直径6mmの金属製シャフトを中心に配設した
直径16.5mm、長さ215mmのウレタンフォーム
帯電ローラを作成した。帯電ローラの硬度は42°であ
った。
【0023】次いで、上記帯電ローラを、第1図に示す
画像形成装置に組み込み、温度、湿度が各々22℃、5
5%の環境で抵抗値を測定したところ1000Vで、1
×108 Ωであった。−1700Vの定電圧電源を帯電
電源として、グレースケール、黒ベタ、白ベタ画像を印
刷したところ良好な画像が得られた。更に、この帯電ロ
ーラの金属製シャフトを除去して厚さ4mmのリング状
試験片を作成し、引っ張り試験を行ったところ破断強度
は1.8kgf/cm2 であった。
【0024】
【発明の効果】本発明の半導電性高分子部材は、低硬度
で、高破断強度であり、かつ所定の抵抗値を与えるもの
であり、これを電子写真プロセスの帯電ローラに利用す
れば、好適な画像が得られるものである。Description: BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a charging device such as an image forming device using a semiconductive polymer member used in an electrophotographic process. 2. Description of the Related Art In recent years, with the advance of electronic technology, a demand for a semiconductive member used in an electrophotographic process has been increased, and in particular, an elastic roller used in a charging process has attracted attention. It is necessary that the semiconductive member used in such applications not only has a predetermined electric resistance value and hardness, but also has sufficient mechanical strength against stress such as rotating while continuously applying pressure. It is. Conventionally, semiconductive members used in such applications include polymer oxides such as polymer elastomers and polymer foams, metal oxide powder, carbon black, lithium perchlorate and sodium perchlorate. Inorganic ionic substances such as inorganic ionic substances, cationic surfactants such as modified aliphatic dimethylethylammonium ethosulfate, organic ionic substances such as quaternary ammonium salts such as tetrabutylammonium borofluoride, and charge transfer complexes can be formed. A polymer member adjusted to a predetermined resistance value by mixing a conductive agent such as an electron accepting substance is used. [0004] Such members need to have low hardness in order to obtain high quality images. In order to reduce the hardness of the polymer member, a method of mixing foam into a foam body, a method of reducing the blending amount of carbon black or the like used as a reinforcing material, a method of changing to a grade having a low degree of reinforcement, oil, etc. Is used. However, simply changing the method of forming a foam body, reducing the amount of reinforcing material, or changing the type of reinforcing material will result in the breaking strength of the member.
Degree is lowered, this kind of members to be used by rotating in a state of normally applying a load of more than 500 g, the breaking strength of the member is broken during long-term use if the lower 2.2 kgf / cm 2 In particular, when the pressure is 2 kgf / cm 2 or less, the frequency of breakage of the member increases. Also,
The method of adding a plasticizer has a problem that the plasticizer bleeds during use for a long period of time and contaminates the photoreceptor. Accordingly, an object of the present invention is to solve the drawbacks of the conventional semiconductive polymer member and to provide a charging device for an image forming apparatus using a semiconductive polymer member having the above-mentioned various characteristics. . The inventors of the present invention have made intensive studies to achieve the above object, and as a result, have made a special method for producing a polyurethane foam, and added a conductive agent thereto. by imparting conductivity, fracture strength degree 2kg
f / cm 2 or more, Asker C hardness of 50 ° or less, and electrical resistance of 1 × 10 4 to 1 × 10 12 Ωcm. Invented the invention. Hereinafter, the present invention will be described in detail. The semiconductive polymer member according to the present invention is obtained by adding and mixing a conductivity imparting agent to a polyurethane foam, and has an electric resistance of 22 V and a relative humidity of 55% at a measurement voltage of 1000 V and a volume resistance of 1%. × 10 4 to 1 × 10 12 Ωc
m, preferably 2 × 10 7 to 5 × 10 11 Ωcm,
Breaking strength degree 2 kgf / cm 2 or more, preferably 2.2k
gf / cm 2 or more and Asker C hardness of 50 ° or less, preferably 42 ° or less. Here, polyurethane foams include polyether polyols, polyester polyols, polybutadiene polyols, polyisoprene polyols, polyols obtained by addition-polymerizing polyethylene oxide or polypropylene oxide to glycerin, ethylene glycol,
Polyol components such as propanediol and butanediol are converted to liquid M such as tolylene diisocyanate (TDI), diphenylmethane diisocyanate (MDI), crude diphenylmethane diisocyanate (crude MDI) and uretonimine-modified diphenylmethane diisocyanate.
The object of the present invention is effectively achieved by including, as a constituent material, a material prepolymerized with an isocyanate such as DI or isophorone diisocyanate. As the chain extender, known polyols such as ethylene glycol, propanediol, and butanediol can be used, but polyols having a molecular weight of 500 or less, preferably 200 or less are particularly preferably used. The object of the present invention can be effectively achieved by using a mechanical floss method (a method of mixing bubbles by mechanical stirring) as a foaming method. The semiconductive polymer member of the present invention comprises the above-mentioned polymer substance as a base material and a conductivity-imparting agent added thereto. There are no restrictions on the conductive agent for imparting conductivity, but powders of metals and metal oxides, whiskers, fillers such as carbon black, and inorganic ionic substances such as lithium perchlorate, sodium perchlorate, and calcium perchlorate And / or lauryl trimethyl ammonium chloride,
Of cationic surfactants such as stearyltrimethylammonium chloride, octadecyltrimethylammonium chloride, dodecylammonium chloride, hexadecyltrimethylammonium chloride, modified aliphatic dimethylethylammonium ethosulfate, lauryl betaine, stearyl betaine, dimethylalkyl lauryl betaine Zwitterionic surfactants such as quaternary ammonium salts such as tetraethylammonium perchlorate, tetrabutylammonium perchlorate and tetrabutylammonium fluoride; and / or antistatic such as hydrophilic polyols and polyesters. Agent, tetracyanoethylene, tetracyanoquinodimethane, benzoquinone, chloranil, anthraquinone,
Electron accepting substances capable of forming a charge transfer complex such as anthracene, dichlorodicyanobenzoquinone, ferrocene, and phthalocyanine can be used, and these compounds are used for the purpose of improving the compatibility with the urethane foam as the base material. An electron-accepting substance capable of forming a derivative or a charge-transfer complex may be used in the form of a complex with an electron-donating substance such as tetrathiafulvalene or lithium. In addition, as long as the effect of the present invention is not impaired, a polymer polyol that is not prepolymerized may be used in combination, or a foaming agent such as water or chlorofluorocarbon may be used in combination. The above-mentioned member is not limited to a shape used for a charging device, but is usually used in the form of a roller having a metal core disposed at the center. Although there is no limitation on the method of forming the roller, a method of polishing with a grindstone or a method of obtaining a self-skinned foam or an elastomer by using a mold adapted to the shape of the roller is generally used. From the viewpoints of environmental safety, noise, image improvement, etc., it is also possible to provide one or more conductive, semiconductive or insulating various coating layers on the charging member of the present invention. . As these various coating layers, for example, nylon or the like is preferably used, and in particular, by forming a copolymer nylon containing 15% by weight or more of nylon 12,
It is possible to improve the charging environment safety. The melting point of this copolymerized nylon is preferably 120 ° C. or less, particularly 70 ° C.
To 120 ° C, particularly preferably 90 to 110 ° C. In this case, the volume specific resistivity of the coating is not limited, but is usually preferably 10 6 to 10 13 Ωcm. For the purpose of adjusting the volume resistivity, one or more metal oxide particles such as carbon black, tin oxide and titanium oxide can be blended. It is also preferable to form the coating layer with a resin layer containing a urethane-modified acrylic resin containing 5 to 70% by weight of an acrylic resin component, and the acrylic resin component having a glass transition temperature in the range of room temperature to 120 ° C. is preferably used. Can be In this case, the volume resistivity of the coating is not limited, but is preferably 10 6 to 10 13 Ωcm. For the purpose of adjusting the volume resistivity, one or more kinds of metal oxide particles such as carbon black, tin oxide and titanium oxide can be blended, and the urethane-modified acrylic resin contains 1 to 50% by weight of a silicone component. % Is also preferred. In addition, a particle size of 3 near the surface of the member to be charged.
Noise can be reduced by arranging particles of 5 to 100 μm. In this case, there is no limitation on the particles, and any of insulating or conductive particles is preferably used, and the insulating particles may be coated with a conductive coating or an elastic material. There is no limitation on the amount of the particles, but 3 parts per 100 parts by weight of the polymer capable of forming a coating film or an elastic material
~ 50 parts by weight are preferred. Hereinafter, the present invention will be described specifically with reference to Examples and Comparative Examples, but the present invention is not limited to the following Examples. The humidity is relative humidity and the hardness is Asker C
Hardness. [Example 1] 100 parts by weight of a polyether-based prepolymer prepared by prepolymerizing polyether polyol having a molecular weight of 5,000 by adding propylene oxide and ethylene oxide to glycerin with tolylene diisocyanate, 1,4-butanediol 6.55 parts by weight, silicone surfactant 2 parts by weight, dibutyltin dilaurate 0.5 part by weight.
01 parts by weight, and 0.015 parts by weight of a modified aliphatic dimethylethylammonium ethosulfate were mixed with a mixer.
The mixture was mechanically foamed, and a mixture thereof was used to prepare a self-skinned urethane foam charging roller having a diameter of 16.5 mm and a length of 215 mm, which was disposed around a metal shaft having a diameter of 6 mm. The hardness of the charging roller was 38 °. Next, the charging roller is incorporated in the image forming apparatus shown in FIG.
% Was measured in an environment of 1% at 1000V.
0 8 Ω. When a grayscale, solid black, and solid white image was printed using a constant voltage power supply of -1700 V as a charging power supply, a good image was obtained. Further, by removing the metal shaft of the charging roller to create a ring-shaped test piece having a thickness of 4 mm, breaking strength of was a tensile test was 2.9kgf / cm 2. Comparative Example 1 Glycerin was added with propylene oxide and ethylene oxide to have a molecular weight of 5000.
100 parts by weight of polyether polyol, 6.03 parts by weight of tolylene diisocyanate, 2 parts by weight of a silicone surfactant, 0.03 parts by weight of dibutyltin dilaurate, 0.015 parts by weight of modified aliphatic dimethylethylammonium ethosulfate Was mixed and mechanically foamed with a mixer, and a urethane foam charging roller with a self-skin having a diameter of 16.5 mm and a length of 215 mm, which was disposed around a metal shaft having a diameter of 6 mm, was prepared from the mixture. The hardness of the charging roller was 35 °. Next, the charging roller is incorporated in the image forming apparatus shown in FIG.
When the resistance was measured in a 5% environment,
× 10 8 Ω. When a grayscale, solid black, and solid white image was printed using a constant voltage power supply of -1700 V as a charging power supply, a good image was obtained. Further, by removing the metal shaft of the charging roller to create a ring-shaped test piece having a thickness of 4 mm, breaking strength of <br/> was subjected to tensile test was 0.6 kgf / cm 2. Comparative Example 2 Propylene oxide and ethylene oxide were added to glycerin to give a molecular weight of 5,000.
100 parts by weight of polyether polyol, 9.15 parts by weight of crude diphenylmethane diisocyanate, 2 parts by weight of a silicone surfactant, 0.003 parts by weight of dibutyltin dilaurate, 0.015 parts by weight of modified aliphatic dimethylethylammonium ethosulfate Was mixed and mechanically foamed with a mixer, and the mixture was used to place a metal shaft having a diameter of 6 mm at the center and a diameter of 16.5 mm and a length of 215 mm.
A self-skinning urethane foam charging roller having a thickness of mm was prepared. The hardness of the charging roller was 38 °. Next, the charging roller is incorporated in the image forming apparatus shown in FIG.
When the resistance was measured in a 5% environment,
× 10 8 Ω. When a grayscale, solid black, and solid white image was printed using a constant voltage power supply of -1700 V as a charging power supply, a good image was obtained. Further, by removing the metal shaft of the charging roller to create a ring-shaped test piece having a thickness of 4 mm, breaking strength of <br/> was subjected to tensile test was 0.2 kgf / cm 2. Comparative Example 3 Propylene oxide and ethylene oxide were added to glycerin to give a molecular weight of 5,000.
100 parts by weight of a polyether prepolymer obtained by prepolymerizing the polyether polyol prepared with tolylene diisocyanate, 6.1 parts by weight of 1,4-butanediol, 0.5 part by weight of distilled water, 0.01 part of dibutyltin dilaurate
13. parts by weight, 0.03 parts by weight of triethylenediamine, and 0.015 parts by weight of a modified aliphatic dimethylethylammonium ethosulfate mixed with a mixer, and the resulting mixture is disposed around a metal shaft having a diameter of 6 mm.
A self-skinning urethane foam charging roller having a length of 5 mm and a length of 215 mm was prepared. Charging roller hardness is 37 °
Met. Next, the charging roller is incorporated in the image forming apparatus shown in FIG.
% Was measured in an environment of 1% at 1000V.
0 8 Ω. When a grayscale, solid black, and solid white image was printed using a constant voltage power supply of -1700 V as a charging power supply, a good image was obtained. Further, by removing the metal shaft of the charging roller to create a ring-shaped test piece having a thickness of 4 mm, breaking strength of was a tensile test was 0.9 kgf / cm 2. [Comparative Example 4] Propylene oxide and ethylene oxide were added to glycerin to give a molecular weight of 5,000.
100 parts by weight of polyether polyol, 15.5 parts by weight of tolylene diisocyanate, 6.55 parts by weight of 1,4-butanediol, 2 parts by weight of a silicone surfactant, 0.01 part by weight of dibutyltin dilaurate, modified fat Mixing and mechanical foaming of 0.015 parts by weight of trimethyl dimethylethylammonium ethosulfate with a mixer, and using the mixture, a urethane foam charging roller having a diameter of 16.5 mm and a length of 215 mm, which is disposed around a metal shaft having a diameter of 6 mm. Created. The hardness of the charging roller was 42 °. Next, the charging roller is incorporated in the image forming apparatus shown in FIG.
When the resistance was measured in a 5% environment,
× 10 8 Ω. Using a constant voltage power supply of -1700 V as a charging power supply, when a gray scale, black solid, or white solid image was printed, a good image was obtained. Further, by removing the metal shaft of the charging roller to create a ring-shaped test piece having a thickness of 4 mm, breaking strength of <br/> was subjected to tensile test was 1.8 kgf / cm 2. The semiconductive polymer member of the present invention has a low hardness, a high breaking strength and a predetermined resistance value, and is used for a charging roller in an electrophotographic process. Then, a suitable image can be obtained.
【図面の簡単な説明】
【図1】画像形成装置の構造を示した一例の概略図であ
る。BRIEF DESCRIPTION OF THE DRAWINGS FIG. 1 is a schematic view of an example showing a structure of an image forming apparatus.
───────────────────────────────────────────────────── フロントページの続き (56)参考文献 特開 平6−200921(JP,A) 特開 平6−16301(JP,A) 特開 平5−318497(JP,A) (58)調査した分野(Int.Cl.7,DB名) G03G 15/02 G03G 15/16 103 ────────────────────────────────────────────────── ─── Continuation of the front page (56) References JP-A-6-200921 (JP, A) JP-A-6-16301 (JP, A) JP-A-5-318497 (JP, A) (58) Field (Int.Cl. 7 , DB name) G03G 15/02 G03G 15/16 103
Claims (1)
り、アスカ−C硬度が50°以下であり、かつ電気抵抗
が1×104 〜1×1012Ωcmであるポリウレタンフ
ォームを構成材料として含む半導電性高分子部材を用い
た画像形成装置の帯電装置であって、該ポリウレタンフ
ォームがプレポリマー化したポリオール成分を原料とし
て含み、かつメカニカルフロス法により発泡されたこと
を特徴とする半導電性高分子部材を用いた画像形成装置
の帯電装置。(57) [Claims] 1. The breaking strength is 2 kgf / cm 2 or more, the Asker-C hardness is 50 ° or less, and the electric resistance is 1 × 10 4 to 1 × 10 12 Ωcm. a charging device of an image forming apparatus using the including semiconductive polymer members of polyurethane foam as the material is, the polyurethane-off
From a polyol component prepolymerized
Included and foamed by mechanical floss method
A charging device of an image forming apparatus using a semi-conductive polymer member, wherein.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP18208894A JP3362969B2 (en) | 1994-08-03 | 1994-08-03 | Charging device |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP18208894A JP3362969B2 (en) | 1994-08-03 | 1994-08-03 | Charging device |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH0844148A JPH0844148A (en) | 1996-02-16 |
| JP3362969B2 true JP3362969B2 (en) | 2003-01-07 |
Family
ID=16112158
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP18208894A Expired - Lifetime JP3362969B2 (en) | 1994-08-03 | 1994-08-03 | Charging device |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP3362969B2 (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2001089547A (en) * | 1999-09-20 | 2001-04-03 | Inoac Corp | Polyurethane foam and method for producing the same |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH05318497A (en) * | 1992-05-18 | 1993-12-03 | Bando Chem Ind Ltd | Manufacture of foam polyurethane roller |
| JP3149085B2 (en) * | 1992-06-29 | 2001-03-26 | 株式会社ブリヂストン | Coating roller surface coating method |
| JPH06200921A (en) * | 1993-01-07 | 1994-07-19 | Hokushin Ind Inc | Semi-conductive roll |
-
1994
- 1994-08-03 JP JP18208894A patent/JP3362969B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0844148A (en) | 1996-02-16 |
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