![]() electrically conductive electrophotographic member
专利摘要:
ELECTRICALLY DRIVING MEMBER ELECTROPHOTOGRAPHIC.It is an electrically conducting electrophotographic member in which the conductivity required for a charging member is insured and the failure of an image attributed to irregular discharge can be minimized regardless of long-term use and usage environment. An electrically conductive electrophotographic member comprising an electrically conductive support and an electrically conductive layer, wherein the electrically conductive layer includes an ion conductive resin that has a quaternary ammonium ion in a molecuia structure such as an agglutinating resin and a carrier molecule represented using the formula (1) or (2) below:(1) (2)where n1 and n2 each independently represent an integer from 1 to 4. 公开号:BR112013022773A2 申请号:R112013022773-7 申请日:2012-03-16 公开日:2020-09-29 发明作者:Kazuhiro Yamauchi;Norifumi Muranaka;Satoru Nishioka;Yuichi Kikuchi 申请人:Canon Kabushiki Kaisha; IPC主号:
专利说明:
[40] [40] As | B4 | 2 | Co9ecio [coco = sMM | O |) 41] a6 [| B4 | 2 | Cioeci | c10 / C11 = 19081] 472 | [42 / A7 | BB] 2 | (den |) den | 402) Table 2 Table 3 | B1 - | Bis (triluoromethylsuifomiDimide | B6 - Tetrafluoro-baric acid [Bg9 - | 1THexyl-methylimidazophile SS Table 4 binder resin Polypropylene glycol bis (2-aminopropyl ether) (average molecular weight: methanol) average molecular weight of phenol resin average weight resol: 960 B: production of elastic cylinders Nos 1 and 2; The raw materials shown in Table 5 were mixed by a cylinder mixer to obtain a non-vulcanized rubber composition. Table 5 SPSS em at SGEITER with az fearing and ion gones in ne ally (GECO) (trade name: EPICHLOMER CG-102 manufactured by | 100 parts by mass Daiso Co., Ltd. Carbon Co ,, Ltd manufactured by DIC Corporation Dipentamethylenethiurama tetrasulfite (trade name: Next, in a crosshead extruder, an apparatus that includes a metal core feeding mechanism and a conductive cylinder unloading mechanism was prepared. A transport rate of the core metal was 80 mm / sec. A grinder that has an internal diameter of 12.5 mm was mounted on the crosshead. The temperature of the extruder and the crosshead were adjusted to 80 ºC. A layer of a non-vulcanized rubber composition has been formed on the circumference of the core metal fed to the “cross”, the core metal being a stainless steel bar that has an outside diameter of 66 mm and a length of 258 mm. Then, the core metal that has the circumferential surface coated with the non-vulcanized rubber composition layer was placed in a hot air vulcanization oven at 170 ° C and heated for 60 minutes to crosslink the non-vulcanized rubber composition layer. . In this way, an elastic layer of rubber was formed. Subsequently, the ends of the elastic rubber layer were cut and removed so that the length of the rubber was 228 mm. Finally, the surface of the elastic rubber layer has been polished by a recovery grinding wheel and shaped into a crown shape that has a central diameter! 12 mm and an average diameter of 11.8 mm at both ends located 90 mm to the left and right of the central portion. In this way, a No 1 elastic cylinder was obtained. Preparation Example B2: production of elastic cylinder No. 2 An elastic cylinder No. 2 was produced in the same way as in elastic cylinder No. 1, except that a non-vulcanized rubber composition obtained by mixing —the raw materials shown in Table 6 below by a cylinder mixer was used. Table 6! Dipentamethylene tyrram tetrasulfide (trade name: sms of Preparation B3: production of elastic cylinder No. 3 A stainless steel bar that has a diameter of 6 mm and a length of 258 mm was arranged inside a cylindrical metal mold. A mixture of liquid silicon rubber that includes the materials shown in Table 7 below was injected and filled into the cylindrical metal mold cavity. Table 7 Liquid silicone rubber (trade name: SE6724 A / B manufactured 100 parts by mass [o Dor cumne aaa ormeemee | Carbon black (trade name: TOKABLACK% 7360SB manufactured 35 parts by mass [o o caca A SPSS) cylindrical metal mold was heated at a temperature of 120 ºC for 8 minutes and cooled to a temperature of 25 ºC. Then, the stainless steel bar that has a layer of silicone rubber formed on its circumferential surface was released from the mold. Subsequently, the silicone rubber layer was treated at a temperature of 200 ºC for 60 minutes to cure the silicone rubber layer. In this way, a No3 elastic cylinder was obtained, an elastic layer that has a thickness of 3.0 mm that is formed on the circumferential surface of the stainless steel bar. Example 1: production of loading cylinder No 1; The elastic cylinder No 1 was immersed once in the No 1 coating solution prepared above to form a coating film of the No 1 coating solution | on the surface of the elastic layer. The immersion coating time was 9 seconds and the immersion coating pull rate was adjusted so that an initial rate was 20 mm / sec and the final rate was 2 mm / sec. The rate was linearly changed between 20 mm / sec and 2 mm / sec. Subsequently, the elastic cylinder 1 which has the coating film formed on its surface was left as it was in an environment at a temperature of 25 ºC for 30 minutes. Then, the elastic cylinder 1 was placed for 1 hour in a hot air circulation dryer set at a temperature of 90 “C. In addition, the elastic cylinder 1 was placed for 1 hour in the hot air circulation dryer set at a temperature of 160 “ºC to react to the coating film. In this way, a surface layer like the electrically conductive layer was formed on the elastic layer. In this way, the loading cylinder No 1 was obtained. The loading cylinder No 1 was subjected to evaluations as follows. Evaluation 1; volume resistivity measurement The current value of the loading cylinder has been measured and the volume resistivity of the loading cylinder No 1 has been calculated using the measurement result. Figures 2A and 2B are explanatory views that illustrate a method for measuring the current value of the loading cylinder. As shown in Figures 2A and 2B, at the same charge as in the charging cylinder when the electrophotographic imaging device is used, the charging cylinder comes into contact with a metal cylinder 22 that has the same curvature as that of the photosensitive member on the electrophotographic apparatus. In this state, the current was fluid and the current value at that time was measured. Figure 2A illustrates bearings 23a and 23b each attached to a weight and a loading cylinder 21 to be tested. Then, the stress is applied vertically and downwards to both ends of the electrically conductive support 11 for the loading cylinder 21. Vertically below the loading cylinder, a metal cylinder 22 is arranged so that the geometric axis of rotation of the cylinder of metal 22 is parallel to that of the loading cylinder 21. As shown in Figure 2B, the loading cylinder is pressed into the bearings 23a and 23b by a drive device, not shown, while the metal cylinder 22 is rotated. The DC voltage of -200 V is applied by a power supply 24 while the metal cylinder 22 is rotated at the same rotational speed as the photosensitive member when the electrophotographic apparatus is used and the charging cylinder 21 is rotated in a way that follows the turning of the metal cylinder 22. After 2 seconds since the voltage is applied, the average time of the fluid current of the metal cylinder 22 was measured by an ammeter À and the average time of the results obtained by the measurement is 5 seconds was calculated. In this evaluation, two No 1 load cylinders to be tested were prepared. One of the No. 1 loading cylinders was placed at a temperature of 23 ºC / humidity of 55% RH (N / Environment) for 48 hours to acclimatize the No. 1 loading cylinder to the ambient N / N. Subsequently, under the same environment, an SN force was applied to each of both ends of the loading cylinder No 1 to bring the loading cylinder No 1 into contact with the metal cylinder having a diameter of 30 mm. The current value was measured while the metal cylinder was rotated at a circumferential speed of 150 mm / s and the electrical resistance value was determined. The other loading cylinder No 1 was placed in an environment at a temperature of 15 º C / humidity of 10% R.H. (Environment L / L) for 48 hours to acclimate the loading cylinder to the environment L / L. Subsequently, under the same environment, an SN force was applied to each of both ends of the loading cylinder No 1 to bring the loading cylinder No 1 into contact with the metal cylinder having a diameter of 30 mm. The current value was measured while the metal cylinder was rotated at a circumferential speed of 150 mm / s and the electrical resistance value was determined. The electrical resistivity of the loading cylinder No 1 under the L / L environment was divided by the electrical resistivity of the loading cylinder No 1 under the N / N environment and converted into the logarithm. The logarithm was defined as an environmental fluctuation digit. Thus, the dependence of the electrical resistivity of the charging cylinder No 1. environmental flotation can be evaluated Evaluation 2: spill assessment: The loading cylinder No. 1 was placed on a sheet of polyethylene terephthalate (PET) and a load of 500 g was applied to each of both ends of the emxo of the loading cylinder No 1 to make the surface of the loading cylinder No 1 contact the PET sheet. This state was maintained under an environment of a temperature of 40 * C / humidity of 95% RH. for a week. Subsequently, the loading cylinder No 1 was removed from the PET sheet and the surface of the PET sheet in contact by the loading cylinder No 1 was observed with an optical microscope (10 times magnification). It was verified whether objects spilled from the elastic layer of the loading cylinder No. 1 through the surface layer of the same and adhered to the surface of the PET sheet and evaluation were made, according to the criteria shown in Table 8 below. Table 8 of PET in contact by the loading cylinder. "Cloudiness" caused by slight adhesion of mixed objects is loading. PET in contact by the loading cylinder. Assessment 3: assessment of loading capacity An electrophotographic laser printer (trade name: Laserjet 4700dn) has been modified so that an emission rate of 200 mm / sec. Loading cylinder No 1 was mounted on the modified laser printer as the loading cylinder. The laser printer has an image resolution of 600 dpi. The laser printer was operated intermittently to form an image and 40001 sheets of an electrophotographic image were emitted. The intermittent operation to form an image means that after two sheets of an image are emitted, the rotation of the electrophotographic photosensitive member drum is stopped for approximately 3 seconds and the operation to form an image is performed again. The image emitted at that time was a character image that has a print density of 1% from the first sheet to the 40,000th sheet and a halftone image for the last sheet. Here, the halftone image was an image in which the horizontal lines were drawn a width of 1 point in the direction perpendicular to the rotational direction of the electrophotographic photosensitive member and an interval of 2 points. The 40,001th sheet of the halftone image was visually observed and evaluation was performed, according to the criteria - shown in Table 9 below. Table 9 seen in the halftone image. LR | eregemento were fixed and in the part of the loading mentom image were found in the halftone image part. seen in the halftone image part. were found in the halftone image. Evaluation 4: evaluation using defects similar to dots in the image The loading cylinder No. 1 was mounted on an electrophotographic laser printer (trade name: Laserjet 4515n, manufactured by Hewlett-Packard Company) as the loading cylinder. The laser printer has a recording medium emission speed of 370 mm / sec and an image resolution of 1200 dpi. The laser printer was operated intermittently to form an image and 40,000 sheets of an electrophotographic image were issued. The intermittent operation to form an image means that after two sheets of an image are emitted, the electrophotographic photosensitive member gyro-drum is stopped for approximately 3 seconds and the operation to form an image is performed again. Í The image emitted at that time was a line image in H. A Line image | in H it was an image in which the horizontal lines were drawn a width of 2 points in the direction perpendicular to the rotational direction of the photosensitive member - electrophotographic and an interval of 176 points. Subsequently, a halftone image was emitted at an AC voltage to be applied of -600 V and a frequency of 2931 Hz, while the AC voltage to be applied was increased from Vpp = 1,200 V. Then, the tension at which the dot-like defects in the image disappeared was measured. According to this assessment, as the dot-like defects in an image disappear at a lower voltage, the electrical resistance value is more uniform in the charging cylinder. Evaluation 5: the molar ratio of the carrier molecule, according to the present invention, to all carrier molecules in the electrically conductive layer The surface layer of the loading cylinder No. 1 was scraped and dissolved in a dilute aqueous solution of hydrochloric acid to extract the carrier molecules in the ion-conducting resin. The aqueous solution after extraction was dried to recover an extracted product. Then, mass spectrometry by a flight time mass spectrometer (TOF-MS) and an ICP light emission analysis was performed to detect the amount of all carrier molecules that exist in the surface layer and the - amount of the molecule carrier in accordance with the present invention. In this way, the molar ratio of carrier molecule according to the present invention to all carrier molecules in the electrically conductive layer was determined. Examples 2 to 42 Loading rollers Nos 2 to 42 were produced in the same way as in the loading cylinder No 1 except that the coating solutions that have a number shown in Table 10 were used for the formation of the electrically conductive layer as the surface layer. These loading cylinders were evaluated in the same way as in the loading cylinder No 1. Table 10 [-— |] evaluation | es volume of solution fluctuates- Valuation Valuation Valuation 5 coating | environment | Ambient environment | tion2 Evaluates- Evaluates (%) ment N / N UL tal tion 3 tion No volume resistivity (KV) 11 | 1 [11607 34668) 149 | A | CC | 144 | o8 | 2 | 2 | giEr6 | 1968! 137 | A | CC | 145 | o | | 3 | 3 | 636X06 25807) 061 | A | A | 146 | & 8 | | 4 | 4 [41606 / 24E% 7) 078 | A | B | 1653 | 98 | | 5 | & | 86E06 | 39E7 | o6s | A | A | 148 | o | [6 [| 6 [55EX06 21E07 | 058 | A | A | 152 | o8 | | 7 | 7 [46606 18EX7 | 059 | B [| A | 157 | e8 | 1 8 | 8 | G66E06 | 29Er7 | o65 | A | A | 145 | 9 | [9 |] and | 8s4Er06] 3268) o58 | A [A | 441 | 68 | 110 | io | / 81E + 06 | 26E07 | 051 [| A | A | 139 | o | [| 12 | 12 | 55E + 06 | / 417E% 7] 087 | A [| B | 1598 | 6 | [13 | 13 | 70E + 06 | 45E% 07] 081 [| A [Og | 4657 | & | | 14 | 14 | 618r06 | 3287] 072 | A | A | 146 | 89 | 215 | 15 [71606 | 4067] 074 | A | B | 165 | 8 | 1 16 | 16 | 68E06 | 33E7] o68 | A | A | 149 | & | [| 17 | 17 | [636E06G | 31E% 7) 06 | A | A | 162 1 88 | [18 | 18 | 66606 | 35E% 07] 073 | A | B | 1654 | 88 | | 19 | 19 [G65E6 45807) 08 | A | B | 163 | 71 |) | 20 | 20 | 7iEX6 | 52607] 08 | A | 8 | 156 | 6 | | 21 | 21 | 68E06 | / 498E7] 08 | A | B | 1561 70 | [| 22 [| 22 | 146 + 7 | 1169] 1900 | The [CC | 14 | 68 | 1 23 | 23 | 66E + 06 | 27Er7] 06! | A | A | 14 | oo | | 24 | 24 | 46Er06 | 25EX7] 074 | B | A [| 138 | eg] | 25 | 25 | 75EM6 | 2587] 053 | A | A | 1365 | o8 | | 28 | 26 | 64E + 06 | 33EX07] 072 | à | B | 14 | 8 | | 27 | 27 | 6oEr6 4367] 085 | A | BB | 7657 | 62 | | 28 | 28 | 776x06 | / 63E67 | 091 | A | B | 1766 | 6 | | 29 | 29 | 64Er06 32EW7] 070 | À | A | 148 | so | | 30 | 30 77 606 42 607] 078 | À | B | 16 8 | [31 | 31 72606 | 33EXW7 | 06978 | A [| A | 152) 8 | | 32 [| 32 | 67EM6G [32607] 068 | A [| JT 163 | and & | 133 | 33 | 718 + 06 / 38E07 | 073 | A | B | 168 | 8 |) | 34 | 34 | 70E06 / a4sesor | 081 A | BB | 1Q517T 70] | 35 | 36 | 74E06 50EX07 | 083 | A | B 7 1588 | AO | 36 | 36 72606 | 51E% 07] 08 | A | B T 155 [| 77) 137 | 37 | g916r06 [15609] 223 A | CEC ST Ta | 68 [38 | 36 [76ErO6 35ErO7 | 066 | A | A | 142 | 98 | [39 | 39 T74EH6 33607] 066 | A | A | 147 | 8th | | 40 | to [89E: 06 | 14EO9 | 220 | A | C [148 [o8 | | N | 4 [| 74E% 06] | [33EM07] 06 | A | A | T43 | 08 | [42 | 42 [71606 | / 34ER7! 068 | A | A [14 | so | Examples 43 to 53 The loading rollers Nos 43 to 53 were produced in the same way as in the loading cylinder No 1 except that the elastic cylinder No 1 was replaced by the elastic cylinder No 2 and the surface layer was formed with the use of coating solutions that have a number shown in Table 11 and have undergone Assessment 1 | a Evaluation 5. The results are also shown in Table 11. Table 11 [| . | aAvalçãot | Digital resistivity Evaluation of image volume Fluctuating N-cm solution. Exem- ple Evaluation- So s to cover- | tion2 Evaluates (%) p ment | Ambien- | Ambien- | Evaluation 4 | No te N / N tel / L | resistivity 3 & v) | volume; 20Et07 [65ETOS | 146 | A | C | 145 | 9 | 1 44 3 [22E + 07 44607] 030 | A | B | 1652 | os | 1 45 | 4 [17E + 07 41607] 038 | A | BB | 158 | 99 | 2.5E + 07 [46E + 07 | 027 | A | B | 137 | 9 | 2.4E + 07 | 5.3E + 07 | 0.35 | A | B | 148 | 91 | 2A4EOT 57EOT | 037 | A | BB | 15 | & 1 48 | 22 j46E07 17EX09 | 157 | A | CC | 141 | os | 2.9E + 07 | 74EO7 | n40 A NB ag | oa | 3.3E + 07 | 76Er07] 036 | A B | 133 | og | 52 | 29 (31607 g1EMO7 | 042 | A jd Bag 3.2E + 07 | 9.0E + 07 | 045 | A | B j 152 [| 8 | Example 54 A stainless steel bar that has a diameter of 6 mm and a length 258 mm was placed inside a cylindrical metal mold. A resin mixture obtained by removing IPA from the No 3 coating solution was injected and filled into the cylindrical metal mold cavity. Then, the cylindrical metal mold was heated at a temperature of 90 ºC for 1 hour and additionally heated at a temperature of 160 "C - for 1 hour Subsequently, the cylindrical metal mold was cooled to a temperature of 25 ºC. Then, the stainless steel bar that has an electrically conductive layer formed on its circumferential surface was released from the mold, the electrically conductive layer that has a thickness of 3.0 mm. This is the loading cylinder No. 54. The loading cylinder No. 54 was submitted to Evaluation 1 to Evaluation5.The result is shown in Table 12. Example 55 | A protective layer was provided on the surface layer of the No10 elastic cylinder, according to the following method. Methyl isobutyl ketone was added to a caprolactone-modified acrylic polyol solution and the solution was adjusted so that the solid content was 10% by weight. The mixed solution was adjusted by adding 15 parts by mass of carbon black (HAF), 35 parts by weight of fine particles of needle-like rutile titanium oxide, 0.1 parts by weight of modified dimethyl silicone oil and 80.14 parts by mass of a mixture of a hexamethylene disocyanate (HDI) butanone oxime block body and isophorone disocyanate (IPDI) in 7: 3 based on 100 parts by mass of the solid content in the solution of acrylic polyol. In that time, the mixture of HDI block and IPDI block was added so that "NCO / OH = 1.0" was satisfied. 210 g of the mixed solution and 200 g of glass beads as a medium that has an average particle size of 0.8 mm were mixed in a 450 ml glass bottle and dispersed for 24 hours using a dispersing machine. ink shaker. After dispersion, 5.44 parts by weight (20 parts by weight equivalent based on 100 parts by weight of acrylic polyol) of crosslinking acrylic particles (trade name: —MRS50G; manufactured by Spoken Chemical & Engineering Co., Ltd .) as resin particles were added and the mixed solution was further dispersed for 30 minutes to obtain a coating material to form a protective layer. The coating material obtained to form a protective layer was applied to the outer periphery of the loading cylinder in Example 10 once by immersion coating and air-dried at normal temperature for 30 minutes or more. Then, the coating material was dried by a hot air circulation dryer set at 90 ° C for 1 hour and additionally dried by a hot air circulation dryer set at 160 * C for 1 hour to form an outer layer on the cylinder loading. The time for immersion coating was 9 seconds and a coating pull rate of —immersion was adjusted so that an initial rate was 20 mm / sec and the final rate was 2 mm / sec. The rate was linearly changed between 20 mm / sec and 2 mm / sec. As defined above, the loading cylinder No. 55 which has a protective layer was produced. The loading cylinder No. 55 was submitted to evaluation 1 to evaluation 5. The result is shown in Table 12 Table 12 Digitiveness of; : Exem- fluctuation Evalu- image Assection UU of volume tion k [if Thesis E] o A [is so NS 33/36 Comparative example 1 A No. 43 coating solution was prepared in the same manner as in Preparation 1-2 (1-2) except that glycidyltrimethylammonium chloride was used as the ion conducting agent. A loading cylinder No C-1 was produced in the same way as in Example 1 except that coating solution No 43 was used to form the surface layer and subjected to Assessments 1 to 5. The result is shown in Table 13. In relation to Evaluation 5, the carrier molecule contained in the electrically conductive layer of the loading cylinder No C-1, according to the present Comparative Example was only chlorine ion. The chlorine ion is not the carrier molecule according to the present invention. For this reason, the result of Evaluation 5 was 0 mol%. Comparative example 2 A No 44 coating solution was prepared in the same way as in (1-2) of Preparation Example | except for the fact that trimethylhexylammonium-bis (trifluoromethanesulfonyl) imide was used as the ion conducting agent. A No-C-2 loading cylinder was produced in the same manner as in Example 1 except that the No 44 coating solution was used to | formation of the surface layer and submitted to Assessments 1 to 5. The result is shown | in Table 13.! The Jon-conducting agent according to the present comparative Example has a reactive functional group. For this reason, the binder resin according to the present comparative Example has the quaternary ammonium group or sulfonate group in the structure - demolecule and is not the ion conducting resin according to the present invention. Comparative example 3 A No. 45 coating solution was prepared in the same manner as in (1-2) of Preparation Example 1 except that stearic acid-bis (trifluoromethanesulfonyl) imide was used as the phon conducting agent. A loading cylinder No C-3 was produced in the same manner as in Example 1 except that coating solution No 45 was used to form the surface layer and subjected to Assessments 1 to 5. The result is shown in Table 13. The ion-conducting agent used in the present comparative example has a group of —carboxyl as the ion exchange group. For this reason, the binder resin, according to the present Comparative Example, has a quaternary ammonium group or a suifonate group in the! | | molecule structure and is not the ion-conducting resin according to the present invention. Table 13 Ns ————; Io Resistivity Evaluation of Example Tuiação Evaluation Es compares 'environmental 2' Evaluates (%) tivo Ambien | Ambien- | resistivity Evalu- [| Es DA Rs [2 Per a e o e | [a dies and the evaluated E Example 56 A No.1 development cylinder was produced in the same manner as in Example 1 except that the elastic cylinder No 3 was used and the No 4 coating solution was used to form the surface. The development cylinder No. 1 was submitted to Evaluation 1, Evaluation 2, Evaluation 5 and Evaluation 6 below. Evaluation 6; electrophotographic imaging test As an electrophotography apparatus, a laser printer (trade name: LBP5409, manufactured by Canon Inc.) was used. The pressure at which the developing cylinder in contact with the photosensitive member and the amount of the developing cylinder to invade the photosensitive member were adjusted so that the amount of toner to be applied to the developing cylinder was 0.35 mg / cm2 . In addition, a toner feed roller made of a soft urethane sponge was provided, the toner feed roller scraping the old toner from the development roller and feeding a new toner to the development roller. The development cylinder No 1 was mounted on the laser printer as the development cylinder and 20,000 sheets of an electrophotographic image were continuously formed, in which the image occurs so that horizontal lines are drawn in a width of 2 points in the direction perpendicular to the rotational direction of the photosensitive member and an interval of 50 points. Subsequently, a sheet of a halftone image was formed. The halftone image was visually observed and evaluated, according to the criteria shown in Table 14 below. The result is shown in Table 15. Table 14 Criteria for evaluation A No change in the density of the image synchronized with the rotation cycle of the development cylinder is observed. A clear change in density synchronized with the turning cycle of the development cylinder is observed. Examples 57 to 59 Developing cylinders Nos 2 to 4 were produced in the same manner as in Example 56 except that coating solutions that have a number shown in Table 15 were used to form the surface layer and subjected to Assessments 1, 2, 5 and 6. The results are also shown in Table 15. Table 15 o Evaluation digit resistivity ; tion of tion 2 tion 6 ment | Ambien- | Ambien- tivity (%) No | tenNN | tell | Volume MESstvicade 1,4E + 07 | 35E + 67 | 039 [A | go] A 2.0E + 07 | 39E + 07 | —O28 | A | o8 | A | | 58 | 14 | 19607 44607] o36 Ú | ÀÂÀÚaAaA Pa | 58 | 25 | 26E + 7 61807] o37 | A | ego | Comparative example 4 A C-4 development cylinder was produced in the same manner as in Example 56 except that coating solution No 4 was replaced with coating solution No 44 to form the surface layer and subjected to Assessments 1, 2, 5 and 6. The result is shown in Table 16. The ion-conducting agent, according to the present Comparative Example, has no reactive functional group. For that reason, the binder resin according to the present comparative Example has no quaternary ammonium group or sulfonate group in the molecule structure and is not the ion conductive resin according to the present invention. Table 16 Digit volume resistivity of; Environmental N / N of tion 2 (o) tion 6 Environment Environment L / L | volume resistivity 4 | 15E + 07 40607 | the JJ g | ago no List of numerical references 11 Core metal 12 Elastic layer 13 Surface layer 14 Intermediate layer This application claims the benefit of Patent Application No. JP 2011-062717, filed on March 22, 2011 and Patent Application No. JP JP 2012-051718, filed on March 8, 2012 which are hereby incorporated by reference to this document in its entirety.
权利要求:
Claims (9) [1] 1. Electrically conductive electrophotographic member comprising an electrically conductive support and an electrically conductive layer, characterized by the fact that the electrically conductive layer comprises an ion conducting resin that has a quaternary ammonium ion in a molecule structure such as a binder resin, and a carrier molecule represented by the following formula (1): (1) R F AND F F o. Nn7 / So NT o do [2] 2. Electrically conductive electrophotographic member comprising an electrically conductive support and an electrically conductive layer, characterized by the fact that: the electrically conductive layer comprises an ion conducting resin that has a quaternary ammonium ion in a molecule structure such as a binder resin, and a carrier molecule represented by the following formula (5): (5) o R $ O In which the carrier molecule represented by formula (5) is selected from the group consisting of ethyl sulfonate, n-butyl sulfonate, sec-butyl sulfonate, tert-butyl sulfonate, n-octyl sulfonate, and n-decyl sulfonate. [3] 3. Electrically conductive electrophotographic member comprising an electrically conductive support and an electrically conductive layer, characterized by the fact that the electrically conductive layer comprises an ion conducting resin that has a sulfonic acid fon in a molecule structure such as a binder resin, and a carrier molecule represented by the following formula (6) or (7): (6) (7) Rg FA R5 “and R7 ARA | R2 Ra PP No R3 | Re where R ', R3, R4, R5, Ro, R; and Rg, each independently represents hydrogen or a hydrocarbon group having 1 to 10 carbon atoms and can include a hetero atom. [4] 4. Electrically conductive electrophotographic member comprising an electrically conductive support and an electrically conductive layer, characterized by the fact that: the electrically conductive layer comprises an ion conducting resin that has a sulfonic acid fon in a de-molecule structure as a binder resin , and a carrier molecule represented by the following formula (8) or (9): (8) (9) Rua Ú) R 3! R '“| and & "R $ DR R12 where Ro, Rio, R11, Ri2, Ri3 And Ru, each independently represents a hydrocarbon group having 1 to 10 carbon atoms and may include a heteroatom. [5] 5. Electrically conductive electrophotographic member comprising an electrically conductive support and an electrically conductive layer, characterized by the fact that: the electrically conductive layer comprises an ion conducting resin that has a sulfonic acid ion in a molecule structure such as a binder resin, and a carrier molecule represented by the following formula (10): (10) R18 RP R 15 | Ev R16 wherein Ri15, Ri6, R17 and Ri8, each independently represents hydrogen or a hydrocarbon group having 1 to 10 carbon atoms and can include a heteroatom. [6] 6. Electrically conductive member according to any one of claims 1 to 5, characterized in that the molecule structure of the ion-conductive resin has an ethylene oxide unit. [7] 7. Electrically conductive member according to claim 6, characterized by the fact that the ion conductive resin is a phenol resin. [8] 8. Electrophotographic apparatus characterized by the fact that it comprises an electrically conductive member of the type defined in any one of claims 1 to 7. [9] 9. Process cartridge characterized by the fact that it comprises an electrically conductive member of the type defined in any one of claims 1 to 7, the process cartridge being detachably fixed to a main body of an electrophotographic apparatus.
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同族专利:
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引用文献:
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法律状态:
2020-10-06| B06U| Preliminary requirement: requests with searches performed by other patent offices: procedure suspended [chapter 6.21 patent gazette]| 2021-01-19| B11B| Dismissal acc. art. 36, par 1 of ipl - no reply within 90 days to fullfil the necessary requirements| 2021-11-23| B350| Update of information on the portal [chapter 15.35 patent gazette]|
优先权:
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申请号 | 申请日 | 专利标题 JP2011-062717|2011-03-22| JP2011062717|2011-03-22| JP2012051718A|JP5875416B2|2011-03-22|2012-03-08|Conductive member for electrophotography| JP2012-051718|2012-03-08| PCT/JP2012/001851|WO2012127835A1|2011-03-22|2012-03-16|Conductive member for electrophotography| 相关专利
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