US3848305A - Roll for contact fusing thermoplastic particles to substrates - Google Patents
Roll for contact fusing thermoplastic particles to substrates Download PDFInfo
- Publication number
- US3848305A US3848305A US00317975A US31797572A US3848305A US 3848305 A US3848305 A US 3848305A US 00317975 A US00317975 A US 00317975A US 31797572 A US31797572 A US 31797572A US 3848305 A US3848305 A US 3848305A
- Authority
- US
- United States
- Prior art keywords
- roll
- cyclic siloxanes
- coating
- temperature
- weight loss
- 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
- 229920001169 thermoplastic Polymers 0.000 title claims description 10
- 239000004416 thermosoftening plastic Substances 0.000 title claims description 10
- 239000000758 substrate Substances 0.000 title claims description 8
- 239000002245 particle Substances 0.000 title description 5
- -1 cyclic siloxanes Chemical class 0.000 claims abstract description 48
- 230000004580 weight loss Effects 0.000 claims abstract description 17
- 238000000576 coating method Methods 0.000 claims description 22
- 239000011248 coating agent Substances 0.000 claims description 20
- 229920001296 polysiloxane Polymers 0.000 claims description 8
- 239000013536 elastomeric material Substances 0.000 claims description 7
- 239000008187 granular material Substances 0.000 claims description 4
- 229920002379 silicone rubber Polymers 0.000 abstract description 22
- 239000000463 material Substances 0.000 description 43
- 238000000034 method Methods 0.000 description 11
- 239000004945 silicone rubber Substances 0.000 description 9
- 238000004073 vulcanization Methods 0.000 description 9
- 238000009835 boiling Methods 0.000 description 7
- 229920001971 elastomer Polymers 0.000 description 7
- 239000000945 filler Substances 0.000 description 7
- 238000010438 heat treatment Methods 0.000 description 7
- 238000004132 cross linking Methods 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- 230000015556 catabolic process Effects 0.000 description 4
- 125000004122 cyclic group Chemical group 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 239000005060 rubber Substances 0.000 description 4
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 3
- 230000009286 beneficial effect Effects 0.000 description 3
- 239000003054 catalyst Substances 0.000 description 3
- 238000006731 degradation reaction Methods 0.000 description 3
- 230000001627 detrimental effect Effects 0.000 description 3
- 239000012975 dibutyltin dilaurate Substances 0.000 description 3
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000000806 elastomer Substances 0.000 description 3
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- LIVNPJMFVYWSIS-UHFFFAOYSA-N silicon monoxide Inorganic materials [Si-]#[O+] LIVNPJMFVYWSIS-UHFFFAOYSA-N 0.000 description 3
- 230000001052 transient effect Effects 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 238000013459 approach Methods 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 230000002939 deleterious effect Effects 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 238000011282 treatment Methods 0.000 description 2
- 229920004511 Dow Corning® 200 Fluid Polymers 0.000 description 1
- 229910018557 Si O Inorganic materials 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 239000004809 Teflon Substances 0.000 description 1
- 229920006362 Teflon® Polymers 0.000 description 1
- 230000001464 adherent effect Effects 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- HUMHYXGDUOGHTG-HEZXSMHISA-N alpha-D-GalpNAc-(1->3)-[alpha-L-Fucp-(1->2)]-D-Galp Chemical compound O[C@H]1[C@H](O)[C@H](O)[C@H](C)O[C@H]1O[C@@H]1[C@@H](O[C@@H]2[C@@H]([C@@H](O)[C@@H](O)[C@@H](CO)O2)NC(C)=O)[C@@H](O)[C@@H](CO)OC1O HUMHYXGDUOGHTG-HEZXSMHISA-N 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000010073 coating (rubber) Methods 0.000 description 1
- 238000011284 combination treatment Methods 0.000 description 1
- 230000001143 conditioned effect Effects 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 229920006037 cross link polymer Polymers 0.000 description 1
- 239000007857 degradation product Substances 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 239000004205 dimethyl polysiloxane Substances 0.000 description 1
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- UQEAIHBTYFGYIE-UHFFFAOYSA-N hexamethyldisiloxane Chemical compound C[Si](C)(C)O[Si](C)(C)C UQEAIHBTYFGYIE-UHFFFAOYSA-N 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N iron oxide Inorganic materials [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 1
- 210000003127 knee Anatomy 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000013011 mating Effects 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 125000000962 organic group Chemical group 0.000 description 1
- NDLPOXTZKUMGOV-UHFFFAOYSA-N oxo(oxoferriooxy)iron hydrate Chemical compound O.O=[Fe]O[Fe]=O NDLPOXTZKUMGOV-UHFFFAOYSA-N 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 1
- 230000002028 premature Effects 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 230000035882 stress Effects 0.000 description 1
- 238000003878 thermal aging Methods 0.000 description 1
- 238000009489 vacuum treatment Methods 0.000 description 1
- 238000009834 vaporization Methods 0.000 description 1
- 230000008016 vaporization Effects 0.000 description 1
Images
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G15/00—Apparatus for electrographic processes using a charge pattern
- G03G15/20—Apparatus for electrographic processes using a charge pattern for fixing, e.g. by using heat
- G03G15/2003—Apparatus for electrographic processes using a charge pattern for fixing, e.g. by using heat using heat
- G03G15/2014—Apparatus for electrographic processes using a charge pattern for fixing, e.g. by using heat using heat using contact heat
- G03G15/2053—Structural details of heat elements, e.g. structure of roller or belt, eddy current, induction heating
- G03G15/2057—Structural details of heat elements, e.g. structure of roller or belt, eddy current, induction heating relating to the chemical composition of the heat element and layers thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/04—Polysiloxanes
- C08G77/32—Post-polymerisation treatment
Definitions
- ABSTRACT A fuser roll is coated with a silicone elastomer and heat and vacuum cured to remove the cyclic siloxanes to a state of constant weight loss to improve the release of paper and toner from the roll surface.
- thermoplastic toner particles to a porous substrate such as paper in order to render the copies produced by the electrophotographic process, pennanent.
- a porous substrate such as paper
- the thermoplastic powder or toner can be fused by radiant heating, vapor fusing, conductive heating through the paper and fuser roll techniques such as hot rolls or high pressure rolls.
- the fuser roll technique there has been two different approaches, that being the use of a rigid, or non-deforming hot roll and a compliant back-up roll and the other technique being the use of a rigid backup roll and a compliant hot roll.
- the roll which is compliant is generally a sturdy rigid cylinder which is in turn coated with a layer of an elastomeric material which then is deformed in the pressure nip formed by it and its mating roll in the fuser roll apparatus, thus creating a footprint or width where the two roll surfaces intimately engage.
- This footprint or nip is necessary due to the fact that two rigid rolls engaging each other would only provide line contact or at best a very very narrowcontact when engaging the paper and there would be insufficient residence time in which to transfer enough thermal energy to the toner to adequately soften and fuse the toner particles to the paper. If very high loads are applied to rolls with elastomer coating such as to simulate two high pressure metallic rolls, then the elastomer is subject to premature failure due to the very high stresses applied to the elastomer.
- the preferable arrangement within fusing apparatuses implementing the fuser roll technique is to use a deformable or elastomeric coated fuser hot roll and a relatively rigid back-up roll.
- Prior art fuser rolls have been coated with silicone elastomers and in some cases further encased in sleeves of low surface energy materials which do not contain cyclic siloxanesOther approaches to the release problem include use of low energy fillers such as polytetraflouroethylene. Other-fuser rolls use a higher energy roll. This sharp curve or shortened radius is beneficial to release of the copy from the surface of the hot roll since it is very difficult for the toned paper to traverse the short radius thus staying with and wrapping to the hot roll causing a paper feed failure.
- silicone rubbers have a very low surface energy and are generally of the class of materials which are advantageous in this implementation.
- silicone rubbers have several qualities which have prevented wide-spread commercialized use as roll fuser coatings.
- the silicone rubbers have a very low surface energy at room temperature; however, when raised to elevated temperatures for the operation of the roll fuser, the silicone rubbers release properties are greatly deteriorated. Because of the deterioration of the release properties, paper and toner images have a tendency to adhere to the roll and wrap around the roll causing a fuser failure.
- hot roll may be interchangeably used with that of fuser roll and designates the roll which is heated and is forced into engagement with the surface of the paper carrying the unfused toner image.
- back-up roll is used in the sense that it engages the reverse side of the sheet from that carrying the unfused toner image and provides the backing force for the paper to cause intimate engagement between the hot roll surface and the toner image.
- the deformable or elastomeric coated hot roll is preferable because the radius of the roll surface, when deformed, is a much sharper or shorter radius at the exit point of the nip than the undeformed radius of the It is the primary object of this invention to remove cyclic siloxanes from the elastomeric coating material to extend the useful life of a hot roll within a roll fusing apparatus.
- the shortcomings of the prior art are overcome together with the accomplishment of the above objects by the removal of cyclic siloxanes from elastomeric silicone rubber materials used as hot roll fuser coatings.
- the cyclic siloxanes are removed by a simultaneous, combination treatment of heating the coated roll structure to a temperature above the normal operating temperature of the roll and subjecting the roll and coating to a high vacuum during the heating process. This accelerates the removal of cyclic siloxanes and enhances the breakdown by any metastable crosslinks which would otherwise result in cyclic siloxanes liberation later in service in the fuser apparatus thus adversely affest nsrs pjae.
- the FIGURE is a general curve illustrating the weight loss with time at a temperature for a silicone elastomer.
- the above material is of the general form where n equals approximately 1,000. Contained in this material are two filler materials, a first filler material of silicon dioxide (SiO and a second filler material ferric oxide (Fe O In addition to the above three constituents, a fourthsonst tueutis atri un tional. s lane f, the f rm where R is an organic group.
- dibutyltin dilaurate catalyst is provided as a separate material.
- the dibutyltin dilaurate catalyst is added to the four constituents listed above, to initiate the vulcanization or crosslinking of the basic composition. As the vulcanization or crosslinking progresses, an elastomeric, network structure is formed.
- cyclic siloxanes of the general formula -LI tJt where n ranges from 3 to 8, and where the structure is formed into a ring.
- the cyclic siloxanes are present as an impurity in the crosslinked polymer and also are formed by degradation of the polymeric crosslinked structure with thermal aging.
- the chains in the crosslinked structure by natural phenomena, have some bonds which are weaker than others. When the material is heated, energy is provided by which these bonds may be broken and a segment of the longer chain is then separated from the crosslinked structure and continues to break down until such time as n of the general formula for cyclic siloxanes is in the range of from 3 to 8. At elevated temperatures these materials are then chemically stable and exist in either a liquid or vapor state depending on their individual melting and boiling points and the prevailing conditions.
- the cyclic siloxanes have varying boiling points depending on the molecular weights. Some boiling points are sufficiently high that it is necessary to reduce the pressure to a vacuum to volatilize these materials rapidly enough to prevent a build-up of these products. The boiling points are set forth in Table I below.
- the cure temperature must be above the operating temperature of the roll, preferably above the highest boiling point of the material to be removed. Thus, under a pressure of about 20 mms of Hg the cure temperature should be above 3 34F.
- the tempe'rature of a roll in operation is approximately 340 to 380F.
- a temperature of cure of 500F. is both adequate and high enough to provide efficiency of speed when coupled with a vacuum pressure of about 20 mm Hg.
- cyclic siloxanes present in the polymer and formed as degradation products are apparently detrimental to release properties of the silicone rubber coating.
- These cyclic siloxanes are very similar in general structure to materials which have been known as release agents, for example, Dow Corning 200 silicone liquid which is a polydimethylsiloxane.
- the primary difference is thatthe cyclic siloxanes have a detrimental effect on the surface characteristicsof the silicone rubber.
- the cyclic siloxanes have a tendency to make the rubber tacky or sticky whereas it generally has a relatively low surface energy level and thus would not be tacky, sticky, or adherent.
- the prior art teaches the use of polydimethylsiloxanes as release agents, but these are taught with materials other than the silicone rubbers.
- Examples are the use of polydimethylsiloxanes either on steel rolls or on a Teflon (Trademark of DuPont Corporation) surface. It becomes apparent from the difference in performance, that although these cyclic siloxanes may in some environ ments have a beneficial effect, in the present environment of a dry silicone elastomer hot roll, a deleterious effect is observed.
- a roll core is fabricated to the desired dimensions and mounted in a lathe.
- the RTV-60 silicone material is catalyzed using the dibutyltin dilaurate catalyst up to I approximately 0.50 percent by weight.
- This mixture is then doctored onto the roll as the roll is revolved by the lathe, yielding a coating to 60 mils in thickness.
- the roll is then continued to be rotated and cured at room temperature for approximately 24 hours. After the 24 hour curing-at room temperature, the roll temperature is elevated to approximately 150 F. for a four hour period to insure substantially complete vulcanization. After heat treating at 150F. for four hours, the coating of silicone rubber is ground to about a 25-50 mil thickness.
- the roll After grinding to the desired thickness of coating, the roll is placed in a vacuum oven and the temperature of the roll is elevated to approximately 500 F. for a period of 24 hours.
- the vacuum oven is operated at approximately 29 inches of Hg vacuum.
- thjehigh temperatures of approximately 500 F. being substantially above the normal operating temperature of the hot roll, drives off as vapor the cyclic siloxanes which are the reaction residue of the crosslinking action as well as any cyclic siloxanes which were present in the original polymer.
- the temperature at which the roll is maintained breaks any weak bonds in the crosslinked structure of the silicone elastomeric material, thus forming additional cyclic siloxanes.
- the bonds which are broken are those which are least stable and which would break most easily upon the normal heating of the hot roll during operation.
- the high vacuum which is imposed upon the roll during the heating assists the heat in volatilizing the cyclic siloxanes and removing them from the rubber roll.
- FIG. 1 is a general graph of weight loss as a function of time at a preselected temperature and pressure for a sample of RTV-60.
- the region of the curve, in FIG. 1, indicated as 10 illustrates what can be characterized as a transient condition during the period of time when the residual products of vulcanization or crosslinking specifically the cyclic si loxanes are being removed and during which time the temperature of the curing process is generating additional cyclic siloxanes due to the breakage of the weakest or metastable, polymeric bonds of the crosslinked elastomeric material.
- Region 12 of the curve is the region at which stabilization occurs and the rate of removal is reduced due to the fact that excessive residual vulcanization products are no longer available for removal and that the only materials remaining for removal are those being generated on a continuing basis due to the elevated service temperature.
- Region 14 of the curve illustrates the steady state condition which is accomplished as a result of the removal of the vulcanization products and the originally produced cyclic siloxanes due to an initial temperature increase.
- the derivative of weight loss with respect to time yields a constant after the transient cyclic siloxanes have been removed.
- the constant rate of weight loss may be secured under service conditioned by either attaining the constant rate under care, or curing to a high enough point on the curve in either region 10 or 12 that under a reduced service temperature and atmospheric pressure the rate of weight loss in service is substantially constant.
- region 14 It is in that state or condition represented by region 14 where acceptable and reliable release properties of the roll fuser can be obtained.
- the rate of weight loss in regions 10 and 12 may be increased by higher elevations of temperature and/or an increase in the vacuum applied. A decrease in vacuum and/or temperature will decrease the rate of weight loss in these regions 10 and 12 conversely.
- the curve is a general one and with appropriate scale would be applicable to a roll under treatment or in service.
- a roll for fusing thermoplastic granular material to a substrate said roll having a cylindrical core, and a coating on said core of a silicone elastomeric material, the improvement comprising:
- a roll for fusing thermoplastic granular material to a substrate said roll having a cylindrical core, and a coating on said core of a silicone elastomeric material, the improvement comprising:
- said coating having the volatile components thereof, reduced to below the level at which said coating has a substantially constant rate of weight loss for a selected temperature and under a selected nip pressure.
- said volatile components are cyclic siloxanes having the basic unit structure of Where q aliitqjir a M
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Fixing For Electrophotography (AREA)
- Lining Or Joining Of Plastics Or The Like (AREA)
- Rolls And Other Rotary Bodies (AREA)
Priority Applications (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US00317975A US3848305A (en) | 1972-12-26 | 1972-12-26 | Roll for contact fusing thermoplastic particles to substrates |
IT30206/73A IT1006104B (it) | 1972-12-26 | 1973-10-17 | Rullo per la fusione di particelle termoplastiche in particolare per macchine copiatrici elettrosati che |
FR7340557A FR2211346B1 (enrdf_load_stackoverflow) | 1972-12-26 | 1973-11-06 | |
GB5298773A GB1444410A (en) | 1972-12-26 | 1973-11-15 | Roller for fusing thermoplastic particles to substrates and a method of making such a roller |
CA186,212A CA1023624A (en) | 1972-12-26 | 1973-11-20 | Roll for contact fusing thermoplastic particles to substrates |
DE19732363346 DE2363346C3 (de) | 1972-12-26 | 1973-12-20 | Schmelzfixierrolle mit Silikonelastomer-Beschichtung |
JP48143656A JPS5137786B2 (enrdf_load_stackoverflow) | 1972-12-26 | 1973-12-24 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US00317975A US3848305A (en) | 1972-12-26 | 1972-12-26 | Roll for contact fusing thermoplastic particles to substrates |
Publications (1)
Publication Number | Publication Date |
---|---|
US3848305A true US3848305A (en) | 1974-11-19 |
Family
ID=23236084
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US00317975A Expired - Lifetime US3848305A (en) | 1972-12-26 | 1972-12-26 | Roll for contact fusing thermoplastic particles to substrates |
Country Status (6)
Country | Link |
---|---|
US (1) | US3848305A (enrdf_load_stackoverflow) |
JP (1) | JPS5137786B2 (enrdf_load_stackoverflow) |
CA (1) | CA1023624A (enrdf_load_stackoverflow) |
FR (1) | FR2211346B1 (enrdf_load_stackoverflow) |
GB (1) | GB1444410A (enrdf_load_stackoverflow) |
IT (1) | IT1006104B (enrdf_load_stackoverflow) |
Cited By (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3968551A (en) * | 1974-06-12 | 1976-07-13 | Hitachi Metals, Ltd. | Adamite roll containing cobalt |
US3987530A (en) * | 1975-04-11 | 1976-10-26 | International Business Machines Corporation | Heat fuser roll and method of manufacture |
US4029827A (en) * | 1974-07-24 | 1977-06-14 | Xerox Corporation | Mercapto functional polyorganosiloxane release agents for fusers in electrostatic copiers |
US4075390A (en) * | 1974-08-14 | 1978-02-21 | Xerox Corporation | Fusing surface and method for fixing toner |
US4136613A (en) * | 1975-04-30 | 1979-01-30 | Ricoh Company, Ltd. | Fixing apparatus for electrostatic photography |
US4188423A (en) * | 1977-04-06 | 1980-02-12 | Xerox Corporation | Solvent extracted heat fuser member |
US4280263A (en) * | 1977-12-15 | 1981-07-28 | International Business Machines Corporation | Heat fuser roll and method of manufacture |
US4303545A (en) * | 1980-05-19 | 1981-12-01 | International Business Machines Corporation | Hot roll cleaning paste and method |
US4355225A (en) * | 1981-03-30 | 1982-10-19 | Xerox Corporation | Instant-on radiant fuser |
US4357388A (en) * | 1980-11-13 | 1982-11-02 | International Business Machines Corporation | Hot roll fuser |
US4485066A (en) * | 1983-02-08 | 1984-11-27 | International Business Machines Corporation | Method of making elastomer-coated hot roll |
US4518655A (en) * | 1983-11-25 | 1985-05-21 | Xerox Corporation | Fusing member for electrostatographic copiers |
EP0172668A1 (en) * | 1984-08-01 | 1986-02-26 | Xerox Corporation | Fuser member for electrostatographic copiers |
US4719130A (en) * | 1985-06-17 | 1988-01-12 | Toray Silicone Co., Ltd. | Method for producing a toner-fixer roll |
US5443873A (en) * | 1991-11-12 | 1995-08-22 | Sumitomo Rubber Industries, Ltd. | Silicone rubber roller for electrophotography and method of producing the same |
US5834584A (en) * | 1991-11-12 | 1998-11-10 | Sumitomo Rubber Industries Ltd. | Silicone rubber roller for electrophotography and method of producing the same |
US20050158472A1 (en) * | 2002-02-18 | 2005-07-21 | Joachim Karthauser | Methods of treating polymeric subtrates |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4373239A (en) * | 1980-02-27 | 1983-02-15 | Xerox Corporation | Fusing member for electrostatographic copiers |
EP0570010A1 (en) * | 1992-05-14 | 1993-11-18 | Sumitomo Rubber Industries Limited | Silicone rubber roller for electrophotography and method of producing the same |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3225419A (en) * | 1963-11-12 | 1965-12-28 | Interchem Corp | Roller for applying fountain solution in lithographic printing |
US3435500A (en) * | 1964-10-14 | 1969-04-01 | Xerox Corp | Pressure roll and method of manufacturing |
US3686731A (en) * | 1969-10-07 | 1972-08-29 | Shigeyoshi Koori | Silicone rubber bonded to synthetic rubber utilizing organotrihalogenosilane as a primer |
US3731358A (en) * | 1971-05-20 | 1973-05-08 | Addressograph Multigraph | Roll for pressure fusing toner at elevated temperatures |
-
1972
- 1972-12-26 US US00317975A patent/US3848305A/en not_active Expired - Lifetime
-
1973
- 1973-10-17 IT IT30206/73A patent/IT1006104B/it active
- 1973-11-06 FR FR7340557A patent/FR2211346B1/fr not_active Expired
- 1973-11-15 GB GB5298773A patent/GB1444410A/en not_active Expired
- 1973-11-20 CA CA186,212A patent/CA1023624A/en not_active Expired
- 1973-12-24 JP JP48143656A patent/JPS5137786B2/ja not_active Expired
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3225419A (en) * | 1963-11-12 | 1965-12-28 | Interchem Corp | Roller for applying fountain solution in lithographic printing |
US3435500A (en) * | 1964-10-14 | 1969-04-01 | Xerox Corp | Pressure roll and method of manufacturing |
US3686731A (en) * | 1969-10-07 | 1972-08-29 | Shigeyoshi Koori | Silicone rubber bonded to synthetic rubber utilizing organotrihalogenosilane as a primer |
US3731358A (en) * | 1971-05-20 | 1973-05-08 | Addressograph Multigraph | Roll for pressure fusing toner at elevated temperatures |
Cited By (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3968551A (en) * | 1974-06-12 | 1976-07-13 | Hitachi Metals, Ltd. | Adamite roll containing cobalt |
US4029827A (en) * | 1974-07-24 | 1977-06-14 | Xerox Corporation | Mercapto functional polyorganosiloxane release agents for fusers in electrostatic copiers |
US4075390A (en) * | 1974-08-14 | 1978-02-21 | Xerox Corporation | Fusing surface and method for fixing toner |
US3987530A (en) * | 1975-04-11 | 1976-10-26 | International Business Machines Corporation | Heat fuser roll and method of manufacture |
US4136613A (en) * | 1975-04-30 | 1979-01-30 | Ricoh Company, Ltd. | Fixing apparatus for electrostatic photography |
US4188423A (en) * | 1977-04-06 | 1980-02-12 | Xerox Corporation | Solvent extracted heat fuser member |
US4280263A (en) * | 1977-12-15 | 1981-07-28 | International Business Machines Corporation | Heat fuser roll and method of manufacture |
US4303545A (en) * | 1980-05-19 | 1981-12-01 | International Business Machines Corporation | Hot roll cleaning paste and method |
US4357388A (en) * | 1980-11-13 | 1982-11-02 | International Business Machines Corporation | Hot roll fuser |
US4355225A (en) * | 1981-03-30 | 1982-10-19 | Xerox Corporation | Instant-on radiant fuser |
US4485066A (en) * | 1983-02-08 | 1984-11-27 | International Business Machines Corporation | Method of making elastomer-coated hot roll |
US4518655A (en) * | 1983-11-25 | 1985-05-21 | Xerox Corporation | Fusing member for electrostatographic copiers |
EP0172668A1 (en) * | 1984-08-01 | 1986-02-26 | Xerox Corporation | Fuser member for electrostatographic copiers |
US4719130A (en) * | 1985-06-17 | 1988-01-12 | Toray Silicone Co., Ltd. | Method for producing a toner-fixer roll |
US5443873A (en) * | 1991-11-12 | 1995-08-22 | Sumitomo Rubber Industries, Ltd. | Silicone rubber roller for electrophotography and method of producing the same |
US5834584A (en) * | 1991-11-12 | 1998-11-10 | Sumitomo Rubber Industries Ltd. | Silicone rubber roller for electrophotography and method of producing the same |
US20050158472A1 (en) * | 2002-02-18 | 2005-07-21 | Joachim Karthauser | Methods of treating polymeric subtrates |
Also Published As
Publication number | Publication date |
---|---|
GB1444410A (en) | 1976-07-28 |
FR2211346B1 (enrdf_load_stackoverflow) | 1977-03-11 |
FR2211346A1 (enrdf_load_stackoverflow) | 1974-07-19 |
CA1023624A (en) | 1978-01-03 |
DE2363346B2 (de) | 1975-06-26 |
JPS5137786B2 (enrdf_load_stackoverflow) | 1976-10-18 |
JPS4991647A (enrdf_load_stackoverflow) | 1974-09-02 |
IT1006104B (it) | 1976-09-30 |
DE2363346A1 (de) | 1974-07-11 |
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Owner name: MORGAN BANK Free format text: SECURITY INTEREST;ASSIGNOR:IBM INFORMATION PRODUCTS CORPORATION;REEL/FRAME:005678/0062 Effective date: 19910327 Owner name: IBM INFORMATION PRODUCTS CORPORATION, 55 RAILROAD Free format text: ASSIGNMENT OF ASSIGNORS INTEREST.;ASSIGNOR:INTERNATIONAL BUSINESS MACHINES CORPORATION;REEL/FRAME:005678/0098 Effective date: 19910326 |