Patent Grant
10514633
An electrophotographic printing process involves creating an image on a photoconductive surface or photo imaging plate (PIP). The image that is formed on the photoconductive surface is a latent electrostatic image having image and background areas with different electric potentials. When an electrophotographic ink composition containing charged ink particles is brought into contact with the selectively charged photoconductive surface, the charged ink particles adhere to the image areas of the latent image while the background areas remain clean. The image is then transferred to a print substrate (e.g. paper) either directly or by first being transferred to an intermediate transfer member (e.g. a soft swelling blanket) and then to the print substrate.
One component of a liquid electrophotographic printer is a liquid electrophotographic ink developer unit. Such a unit includes a developer roller, which is used to develop and transport a uniform layer of ink onto the photoconductive surface.
Various implementations are described, by way of example, with reference to the accompanying drawings, in which:
Before the present disclosure is described, it is to be understood that this disclosure is not limited to the particular process steps and materials disclosed in this description because such process steps and materials may vary. It is also to be understood that the terminology used in this disclosure is used for the purpose of describing particular examples. The terms are not intended to be limiting because the scope is intended to be limited by the appended claims and equivalents.
It is noted that, as used in this specification and the appended claims, the singular forms “a,” “an,” and “the” include plural referents unless the context clearly dictates otherwise.
As used in this disclosure, “electrostatic printing” or “electrophotographic printing” refers to the process that provides an image that is transferred from a photoconductive surface or photo imaging plate either directly or indirectly via an intermediate transfer member to a print substrate. As such, the image may not be substantially absorbed into the photo imaging substrate on which it is applied. Additionally, “electrophotographic printers” or “electrostatic printers” refer to those printers capable of performing electrophotographic printing or electrostatic printing, as described above. An electrophotographic printing process may involve subjecting the electrophotographic composition to an electric field, e.g. an electric field in the range of 0.1-200 V/μm, for example, 0.1 to 50 V/μm.
As used in this disclosure, the term “about” is used to provide flexibility to a numerical value or range endpoint by providing that a given value or end point may be a little above or a little below the endpoint to allow for variation in test methods or apparatus. The degree of flexibility of this term can be dictated by the particular variable and would be within the knowledge of those skilled in the art to determine based on experience and the associated description in this disclosure.
As used in this disclosure, a plurality of items, structural elements, compositional elements, and/or materials may be presented in a common list for convenience. However, these lists should be construed as though each member of the list is individually identified as a separate and unique member. Thus, no individual member of such list should be construed as a de facto equivalent of any other member of the same list solely based on their presentation in a common group without indications to the contrary.
As used in this disclosure, the “dielectric constant” (ε) is the ratio of the permittivity of a substance to the permittivity of free space. “Dielectric thickness” refers to the ratio of thickness to dielectric constant (i.e. thickness÷dielectric constant).
As used in this disclosure, “specific resistivity” or “electrical resistivity” refers to an intrinsic property that quantifies how strongly a given material opposes the flow of electric current. It may be defined as ρ=R(A/l), where ρ is the specific resistivity, R is the electrical resistance of the specimen, A is the contact area and l is the length or depth of the specimen. Specific resistivity may be measured using ASTM D257.
Concentrations, amounts, and other numerical data may be expressed or presented in this disclosure in a range format. It is to be understood that such a range format is used merely for convenience and brevity and thus should be interpreted flexibly to include not just the numerical values explicitly recited as the limits of the range, but also to include all the individual numerical values or sub-ranges encompassed within that range as if each numerical value and sub-range is explicitly recited. As an illustration, a numerical range of “about 1 wt % to about 5 wt %” should be interpreted to include not just the explicitly recited values of about 1 wt % to about 5 wt %, but also include individual values and subranges within the indicated range. Thus, included in this numerical range are individual values such as 2, 3.5, and 4 and sub-ranges such as from 1-3, from 2-4, and from 3-5. This same principle applies to ranges reciting a single numerical value. Furthermore, such an interpretation should apply regardless of the breadth of the range or the characteristics being described.
In the present disclosure, the term “isocyanate” is meant to be broadly understood as a functional group of atoms composed of units of the form —N═C═O (1 nitrogen, 1 carbon, 1 oxygen).
The present disclosure relates to a liquid electrophotographic ink developer unit. The unit comprises a developer roller, and a secondary roller that co-operates with the developer roller. The developer roller is formed of a material having a specific resistivity of less than 1×106 Ω·cm. The secondary roller is formed of a material having a specific resistivity of 1×104 to 1×109 Ω·cm. In one example, the secondary roller comprises an inner core that is coated with a material having a specific resistivity of 1×104 to 1×109 Ω·cm.
The liquid electrophotographic ink developer unit may include an ink development zone for containing a liquid electrophotographic ink composition. The chamber may be fluidly connected to a reservoir containing a liquid electrophotographic ink composition.
The present disclosure also relates to a liquid electrophotographic ink developer unit. The unit comprises a developer roller, and a secondary roller that co-operates with the developer roller. The developer roller is formed of a material having a specific resistivity of less than 1×106 Ω·cm. The secondary roller comprises a metal core that is coated with a ceramic material.
The present disclosure also relates to a liquid electrophotographic printer comprising a developer roller, and a secondary roller that co-operates with the developer roller. The developer roller is formed of a material having a specific resistivity of less than 1×106 Ω·cm. The secondary roller is formed of a material having a specific resistivity of 1×104 to 1×109 Ω·cm. In one example, the secondary roller comprises an inner core that is coated with a material having a specific resistivity of 1×104 to 1×109 Ω·cm.
In the prior art, a developer roller having a relatively high specific resistivity (e.g. greater than 1×106 Ω·cm) may be employed in a liquid electrophotographic ink developer unit. Such a developer roller can co-operate with metal secondary rollers (e.g. a squeegee and/or cleaner roller) and maintain electric field required to develop the ink. In the prior art, such a developer roller may be produced by doping a polymer (e.g. polyurethane rubber) with a lithium salt. Lithium salts can be used to provide the developer roller with the amount of ionic conductivity required to acquire and retain an electric field necessary to develop an ink. The conductivity provided by lithium salts, however, may vary depending on environmental factors, for example, temperature and humidity. This can affect the consistency of the image produced. Moreover, over time, the lithium salt may leach out of the roller, reducing its conductivity. The lithium salts may also cause parts (e.g. metal parts) of the printer to corrode. Furthermore, leached lithium ions may contact the photo-imaging plate, causing the surface of the photo-imaging plate to become conductive. If the latter occurs, it may become difficult to appropriately charge the photo-imaging plate, leading to a poorly formed latent image. This, in turn, may affect the overall quality of the final print.
The lithium salt may be replaced with a conductive filler, which may be less prone to leaching. An example of such a conductive filler is carbon black. The present inventors, however, have found that it can be difficult to control the resistivity of the resulting developer roller in the region previously achieved using lithium salts. This is because resistivities in this region can be very sensitive to filler concentrations, particle size distribution and process parameters, such as dispersion uniformity, mould orientation, curing conditions and even flow patterns. Slight variations in these parameters can have a large effect on the resistivity of the overall composition. As a result, a developer roller having resistivities of, for example, greater than 1×106 Ω·cm can be difficult to produce in a reliable manner using conductive fillers, such as carbon black.
It has now been found that it is easier to control the resistivity of the developer roller if its resistivity is reduced to levels below 1×106 Ω·cm. For example, as can be seen in
Developer Roller
The developer roller is formed of material having a specific resistivity of less than 1×106 Ω·cm, for example, 1×103 to less than 1×106 Ω·cm. In one example, the material used to form the developer roller has a specific resistivity of 1×104 Ω·cm to 5×105 Ω·cm. The material may have a specific resistivity of 2×104 Ω·cm to 3×105 Ω·cm, for example, 4×104 Ω·cm to 1×105 Ω·cm. In one example, the material may have a specific resistivity of 5×104 Ω·cm to 8×104 Ω·cm.
In one example, the developer roller comprises a central shaft (e.g. metal) that is coated with a layer (e.g. polymer layer). The layer may coat the central shaft directly. Accordingly, the layer may be in contact with the central shaft. The layer may be outermost layer of the developer roller. The layer may be 0.1 to 3 cm thick, for example, 0.2 to 2 cm thick. In one example, the layer is 0.3 to 1 cm thick, for instance, 0.4 to 0.5 cm thick. The layer may have a specific resistivity of 1×103 to less than 1×106 Ω·cm. In one example, the layer may have a specific resistivity of 1×104 Ω·cm to 5×105 Ω·cm. The layer may have a specific resistivity of 2×104 Ω·cm to 3×105 Ω·cm, for example, 4×104 Ω·cm to 1×105 Ω·cm. In one example, the layer may have a specific resistivity of 5×104 Ω·cm to 8×104 Ω·cm. In one example, the developer roller comprises a central shaft that is coated with one or more layers. Each of the layers may have a specific resistivity of less than 1×106 Ω·cm, for example, 1×103 to less than 1×106 Ω·cm. The combined thickness of the layers may be 0.1 to 3 cm thick, for example, 0.2 to 2 cm. In one example, the combined thickness is 0.3 to 1 cm thick, for instance, 0.4 to 0.5 cm.
Specific resistivity is an intrinsic property that quantifies how strongly a given material opposes the flow of electric current. It may be defined as ρ=R(A/l), where ρ is the specific resistivity, R is the electrical resistance of the specimen, A is the contact area and l is the length or depth of the specimen. Specific resistivity may be measured using ASTM D257. In one example, the specific resistivity may be determined from a disc formed of the material used to form the developer roller having a known thickness (e.g. 2 mm). The disc may be sandwiched between 2 electrodes of a known size (e.g. 30 mm diameter). A known voltage (e.g. 100V DC) may be applied across the electrodes (e.g. for 1 second at 25 degrees C.) and the resistance measured. Specific resistivity may be calculated from the resistance measurement using the electrode contact area and disc thickness. Prior to measuring the specific resistivity of the developer roller, the roller or material used to form the developer roller may be conditioned at a specific humidity and temperature for a period of time. For example, the developer roller or material used to form the developer roller may be conditioned at 50% humidity and 20 degrees C. for 5 or more days, for example, 5 to 10 or 15 days. In one example, the developer roller or material (e.g. polymer composition) used to form the developer roller may be conditioned at 50% humidity and 20 degrees C. for 5 days.
In one example where the roller comprises a central roller shaft and a polymer layer, the specific resistivity may be determined by applying a potential difference between the surface of the roller and the central roller shaft. A known voltage (e.g. 100V DC) may be applied between the central roller shaft and a contact electrode placed on the surface of the roller (e.g. for 1 second at 25 degrees C.) and the resistance measured. Specific resistivity may be calculated from the resistance measurement using the electrode contact area and thickness of the polymer coating.
In some examples, the developer roller may comprise a layer formed from a polymer composition containing a conductive filler. The conductive filer may be dispersed in a polymer resin matrix. Examples of suitable conductive fillers include carbon nanotubes, graphene, carbon fibre, carbon black, metal particles, conductive oxide particles and intrinsic conductive polymer (ICP) particles. In one example, the conductive filler is carbon black.
The conductive filler may be present at a concentration of 0.1 to 20 weight % of the polymer composition. In one example, the conductive filler may be present at a concentration of 0.1 to 5 weight %, for instance, 0.1 to 3 weight %. In one example, the amount of conductive filler (e.g. carbon black) may be 0.1 to 2 weight %, for instance, 0.5 to 1 weight % (e.g. 0.9% in weight).
By selecting types of conductive fillers and controlling the concentration of conductive filler, the developer roller with a target specific resistivity can be obtained. For example, carbon black can be categorized by its structure. Carbon black may comprise nearly spherical primary particles, which are fused together to form aggregates. The degree of aggregation of the particles is known as “structure”. A carbon black with aggregates that are composed of many primary particles, such that there is considerable branching and chaining within an aggregate, is referred to as a high-structure carbon black. If an aggregate consists of relatively few primary particles, the carbon black is referred to as a low-structure black. A developer roller formulation using a high structured carbon black may reach its percolation at a lower concentration compared with a formulation using low structured carbon black.
The concentration of conductive filler may be varied or controlled to provide the developer roller with a target specific resistivity. The conductive filler may be present in the polymer resin matrix in an amount to provide the polymer composition of the developer roller with a specific resistivity of less than 1×106 Ω·cm, for example, 1×104 Ω·cm to less than 1×106 Ω·cm, for instance, 2×104 Ω·cm to 5×105 Ω·cm. The conductive filler may be present in an amount sufficient to provide the polymer composition of the developer roller with a specific resistivity of 2×104 Ω·cm to 3×105 Ω·cm, for example, 4×104 Ω·cm to 1×105 Ω·cm or 5×104 Ω·cm to 8×104 Ω·cm.
The polymer composition may comprise an elastomer. The polymer composition may include a resin matrix that consists essentially of an elastomer. Examples of suitable polymer resin materials include natural rubber, synthetic rubber, polyurethane, nitrile rubber, and epichlorohydrin (1-chloro-2,3-epoxypropane).
In one example, the polymer resin matrix of the polymer composition is formed of a polyurethane. Suitable polyurethanes may be prepared by reacting a polyol with an isocyanate compound, for example, a diisocyanate or polyisocyanate. Suitable polyols include polyester or polyether polyols. The conductive filler may be added to the polyol and/or the isocyanate compound prior to reaction with the isocyanate compound to incorporate the conductive filler into the polyurethane matrix.
In one example, the polyol may be a polyol containing a polyether functional group or a polycaprolactone polyol. Where a polyether functional group is employed, the polyol may be ethoxylated, whereby it contains a functional group having at least 2 carbon atoms between oxygen atoms. The moiety may be derived from at least one of ethylene glycol, di(ethylene glycol), tri(ethylene glycol), tetra(ethylene glycol), poly(diethylene glycol), poly(ethylene oxide) or mixtures thereof. The moiety may be present in the polyol chain or at the terminus.
As mentioned above, isocyanate compounds may be used to react with the polyol to produce the polyurethane. Isocyanate compounds may include, but are not limited to, a diisocyanate or their polymeric derivatives, such as tolulenediisocyanate, Methylene diphenyl diisocyanate (MDI), xylylenediisocyanate, naphthylenediisocyanate, paraphenylenediisocyanate, tetramethylxylenediisocyanate, hexamethylenediisocyanate, 4,4-dicyclohexylmethanediisocyanate, isophoronediisocyanate, or tolidinediisocyanate. Examples of polymeric diphenylmethane diisocyanate (PMDI) are Mondur MR-Light or Mondur MR (Covestro®).
Suitable polyols include polyester polyols containing polyester groups, for example, aliphatic polyester polyol. In one example, the polyol is a branced aliphatic polyester polyol, for example, as sold under the trademark Stepanpol® PC-505P-60 (Stepan) or Lexorez® 1100-35R (Inolex). Other examples include polyether polyols, such as polyethylene glycols sold under the trademark of Carbowax® 1000 (DOW). Other examples include polycaprolactone polyols, for example, sold under the trademark Capa 2010A® (Perstorp).
In one example, the polymer composition of the developer roller may have a Shore A hardness of 20-70, for example, 30-50. In one example, the polymer composition has a Shore A hardness of 30 to 40. The Shore A durometer may be measured according to ASTM Method D2240-86.
The polymer composition of the developer roller may be sufficiently resilient to co-operate with other rollers in the electrophotographic printer, for example, the photoconductive plate, squeegee roller and/or cleaner roller.
In one example, the developer roller is formed of a polymer composition that contains less than 5 weight % lithium salt, for example, less than 2 weight % lithium salt. In one example, the polymer composition contains less than 1 weight % lithium salt, for instance, less than 0.5 weight % or less than 0.2 weight % lithium salt. In another example, the polymer composition is substantially devoid of lithium salt.
The developer roller may comprise an inner core and an outer layer. The inner core may be made of metal or other conductive material. The inner core may be rigid enough to support the outer layer as well as interact with secondary roller(s) within an ink developer unit and/or the photoconductive surface. In one example, the inner core takes the form of a cylindrical rod. Where a metal or conductive material is used to form the inner, the metal or conductive material may be sufficiently conductive to allow charge to transfer from the inner core and into the outer layer.
The outer layer may be formed of a polymer composition as described in this disclosure. In other words, the outer layer may be formed from a polymer composition containing a conductive filler, whereby the polymer composition has a specific resistivity of less than 1×106 Ω·cm, for instance, 1×104 to less than 1×106 Ω·cm. The polymer composition may be in direct contact with the inner core. The polymer composition may be cast, moulded or extruded onto the inner core, for example, a metal core to form the roller. The polymer composition may be present on the external surface of the roller.
Secondary Roller
As mentioned above, it can be difficult to maintain an appropriate electric field for ink development and/or compaction between a developer roller having a specific resistivity of below 1×106Ω and prior art metal secondary rollers. By using a secondary roller formed from a material having a specific resistivity in the range of 1×104 to 1×109 Ω·cm, the risk of breakdown may be reduced.
In the present disclosure, the secondary roller is formed of a material that has a specific resistivity of 1×104 to 1×109 Ω·cm, for example, 1×105 or 1×106 to 5×108. In another example, the material may have a specific resistivity of 8×106 to 2×108 Ω·cm.
The material having a specific resistivity of 1×104 to 1×109 Ω·cm may have a dielectric constant (ε) of 1 to 50, for example, 10 to 20.
In one example, the secondary roller comprises an outer coating formed of a material having a specific resistivity of 1×104 to 1×109 Ω·cm, for example, for example, 1×105 or 1×106 to 5×108. In another example, the coating may have a specific resistivity of 8×106 to 2×108 Ω·cm.
The outer coating may be 2 μm to 2 mm thick. In one example, the coating may be 10 to 1000 μm thick, for example, 50 to 700 μm thick. In one example, the coating may be 100 to 500 μm thick.
The outer coating may have a dielectric thickness (thickness÷dielectric constant (ε)) of 5 μm or greater, for example, 5 to 200 μm.
The secondary roller may comprise a ceramic material. The ceramic material may be formed of a metal oxide or mixtures of metal oxides. The ceramic material may have a specific resistivity of 1×104 to 1×109 Ω·cm, for example, 1×105 or 1×106 to 5×108. In another example, the material may have a specific resistivity of 8×106 to 2×108 Ω·cm.
The resistivity can be adjusted by using a mixture of metal oxides. The ceramic material may be alumina-titania or other combinations of metal oxides. Examples of suitable metal oxides include aluminium oxides, titanium oxides, zirconium oxides, chromium oxides, yttrium oxides and hafnium oxides. Mixtures of two or more of these oxides may be employed. In one example, the ceramic material comprises alumina in an amount of 50 to 80 weight % and titania in an amount of 20 to 50 weight %.
The specific resistivity of the material used to form the secondary roller (e.g. ceramic material or metal oxide) may be determined using any suitable technique. In one example, the method according to ASTM D257 may be used. For example, the material (e.g. ceramic or metal oxide) may be formed into a disc having a known thickness (e.g. 2 mm). The disc may be sandwiched between 2 electrodes of a known size (e.g. 30 mm diameter). A known voltage (e.g. 100V DC) may be applied across the electrodes (e.g. for 1 second at 25 degrees C.) and the resistance measured. Specific resistivity may be calculated from the resistance measurement using the electrode contact area and disc thickness.
In one example, the secondary roller comprises an inner core, for instance, formed of metal. The core may take the form of a metal cylinder. The metal cylinder may function as the roller shaft. The metal core may be coated with a material. The coating (e.g. outermost coating) may have a target specific resistivity. In one example, the secondary roller comprises a core (e.g. a metal core) that is coated (e.g. as outermost coating) with a ceramic material, such as alumina-titania, or a metal oxide (e.g. as described above). The coating may be applied, for example, by plasma spraying. The coating may be 20 to 1000 μm thick, for example, 50 to 700 μm thick. In one example, the coating may be 100 to 500 μm thick, for instance 200 to 400 μm thick.
The secondary roller may comprise a squeegee roller. A squeegee roller may be used to remove any excess solvent (e.g. an organic solvent, for instance, iso-paraffin oil) away from any liquid electrophotographic composition on the developer roller. Depending on the charge of the ink particles, the squeegee roller may be more or less negatively charged relative to the developer roller. In use, as the squeegee roller may come into contact with the developer roller. The ink layer on the developer roller may become more concentrated as pressure is applied to the ink layer by the squeegee roller to remove solvent (e.g. organic solvent) from the surface of the developer roller. This is sometimes referred to as “compaction”. In one example, the squeegee roller may help to develop the ink layer and remove enough solvent from the ink such that the particle concentration is increased.
The secondary roller may additionally or alternatively comprise a cleaner roller. A cleaner roller may be used to remove excess ink from the developer roller after the bulk of the ink has been transferred to the photo-imaging plate. The cleaner roller may have a different charge bias compared to the developer roller so that charged ink particles on the developer roller may be attracted to the cleaner roller and thereby removed from the developer roller.
In one example, the secondary roller may comprise more than one roller. In one example, the secondary roller comprises two or more rollers (e.g. a squeegee roller and a cleaner roller). Each secondary roller may comprise a material having a specific resistivity of 1×104 to 1×109 Ω·cm. All secondary rollers that co-operate with the developer roller may have the same or substantially the same specific resistivity.
Ink Developer Unit
In addition to the developer roller (120), the binary image development unit (105) may include a back electrode (150), a main electrode (145), a squeegee roller (125), a cleaner roller (130), a wiper blade (135), a sponge roller (140), an ink chamber (155), an ink reservoir (160), an ink inlet (170), and an ink outlet (185). The liquid electrophotographic printer (100) therefore may include the binary image development unit (105) mentioned above as well as a photo imaging plate (115) coupled to a photo imaging drum (110) and an imager (165). Each of these will now be discussed in more detail.
The binary image development unit (105) selectively coats the photo imaging plate (115) with an amount of ink. To accomplish this, separate ink tanks may be used to hold and control the desired properties of the ink such as the ink's density and conductivity. One ink tank may be used for each colour. In an idle stage, for example, before printing starts, the binary image development unit (105) may be empty (i.e. devoid of ink). To start developing ink, the binary image development unit (105) may be provided with a flow of ink pumped from ink tanks (not shown) through the ink inlet (170) that allows a continuous supply of ink in the development area or zone, i.e., the gaps (173, 175) between developer roller (120) and electrodes (150, 145). As mentioned earlier, the ink may be positively or negatively charged. For purposes of simplicity in illustration, the ink within the binary image development unit (105) in
As the ink is pumped into the ink chamber (155) via the ink inlet (170), two electrodes, a main electrode (145) and a back electrode (150), apply an electric field across two gaps (173, 175). A first gap (173) is located between the main electrode (145) and the developer roller (120), and a second gap (175) is located between the back electrode (150) and the developer roller (120). The electric charge across these gaps (173, 175) causes the ink particles to be attracted to the more positively charged developer roller (120).
The developer roller (120) may be made of a polyurethane material with an amount of conductive filler, for example, carbon black mixed into the material. As discussed above, this may give the developer roller (120) the ability to hold a specific charge having a higher or lower negative charge compared to the other rollers (125, 110, 130) with which the developer roller (120) directly interacts. As discussed above, the developer roller (120) may contain sufficient conductive filler, whereby the roller (120) has a specific resistivity of less than 1×106 Ω·cm, for example, 5×104 to 1×105 Ω·cm.
In one example, the electrical bias between the electrodes (145, 150) and the developer roller (120) produces an electric field between the electrodes (145, 150) and the developer roller that is about 800-1000 volts. With a gap (173, 175) of about 400-500 μm, the electric field becomes relatively high and the negatively charged ink particles are attracted to the developer roller (120). This creates a layer of ink over the developer roller (120).
As the ink particles are built up on the developer roller (120), a squeegee roller (125) may be used to squeeze the top layer of oil away from the ink. The squeegee roller (125) may also develop some of the ink onto the developer roller (120). In order to accomplish these two objectives, the squeegee roller (125) may be both more negatively charged relative to the developer roller (120) and may abut the developer roller (120) creating a nip. As the squeegee roller (125) comes in contact with the developer roller (120), the ink layer on the developer roller (120) may become more concentrated. In one example, the squeegee roller (125) may develop the ink layer and remove enough oil or organic solvent from the ink such that the particle concentration is increased. In one example, the resulting ink concentration may be around 20% to 25% colorant concentration.
After the ink on the developer roller (120) has been further developed and concentrated by the squeegee roller (125), the ink may be transferred to the photoconductive photo imaging plate (115). In one example, the photo imaging plate (115) may be coupled to a photo imaging drum (110). In another example, the photo imaging drum (110) may incorporate the photo imaging plate (115) such that the photo imaging drum (110) and photo imaging plate (115) are a single piece of photoconductive material. However, for the purposes of simplicity in illustration, the photo imaging plate (115) and photo imaging drum (110) are separate pieces thereby allowing the photo imaging plate to be selectively removed from the photo imaging drum (110) for replacement if needed.
In one example, prior to transfer of ink from the developer roller (120) to the photo imaging plate (115), the photo imaging plate or, alternatively, the photo imaging drum (110) and plate (115), may be negatively charged with a charge roller. A latent image may, therefore, be developed on the photo imaging plate (115) by selectively discharging selected portions of the photo imaging plate (115) with, for example, a laser (165). The discharged area on photo imaging plate (115) may now be more positive as compared with developer roller (120), while the charged area of photo imaging plate (115) may still relatively be more negative as compared with developer roller (120). When the developer roller (120) comes in contact with the photo imaging plate (120) the negatively charged ink particles may be attracted to the discharged areas on the photo imaging plate (115) while being repelled from the still negatively charged portions thereon. This can create an image on the photo imaging plate (115) which may then be transferred to another intermediate drum or directly to a sheet of media such as a piece of paper.
Because a portion of the ink is transferred from the developer roller (120) to the photo imaging plate (115), the excess ink may be removed from the developer roller (120) using a cleaner roller (130). The cleaner roller (130) may have a more positive bias compared to the developer roller (120). As such, the negatively charged ink particles may be attracted to the cleaner roller (130) and thereby removed from the developer roller (120). A wiper blade (135) and sponge roller (140) may subsequently remove the ink from the cleaner roller (130).
The developer roller (120) may be compliant with the other rollers with which it interacts; namely the squeegee roller (125), the cleaner roller (130), and the photo imaging plate (115) and drum (110). These rollers (125, 130) and the photo imaging plate (115) may be made of hard materials such as metal. Therefore, the developer roller (120) may be made of a material that has a low hardness value compared to these other rollers (125, 130), the photo imaging plate (115), and the photo imaging drum (110).
As discussed above, the squeegee roller (125) and/or cleaner roller (130) may be formed from a ceramic material. For example, the squeegee and/or cleaner roller may be formed with a metal core that is coated with a ceramic (e.g. alumina/titania), for instance, by plasma spraying.
The developer roller may be at a different bias against the electrodes or secondary roller(s). The difference may be 0 to 1200V. The resistance along a one-meter length of contact nip between the developer roller or any secondary roller may be 3×102 Ohm to 3×105 Ohm or 3.3×102 Ohm to 3.3×105 Ohm, for example, 1.3×104 Ohm to 3×105 Ohm.
In this example, developer rollers produced using the formulation shown in Table 1. The formulation contained carbon black in a concentration below the percolation limit. 99.8 grams of a branched aliphatic polyester polyol (Stepanpol® PC-505P-60 (Stepan Company)) was mixed with 0.2 gram of Ketjenblack EC-600JD Powder (AkzoNobel) and other additives through a high shear mixer. The mixture was then degassed at 90 degrees C. and 635 torr vacuum for 16 hours. The mixture temperature was increased to 105 degrees C. 10.7 g polymeric isocyanates based on diphenyl methane diisocyanate (Mondur® MR light supplied by Covestro®) were added and the mixture was mixed using a dual asymmetric centrifugal mixer for 3 minutes. The final liquid was then poured into a tube-type casting mould with a metal developer roller core positioned inside. The composition was cured at temperatures about 120 degrees C. for 3 hours before demoulding. The resulting rollers were then conditioned at 50% humidity and 20 degrees C. for more than 5 days before specific resistivities of the rollers were determined. The specific resistivities of the rollers from this process ranged from greater than 1.0×106-1.0×107 Ω·cm. Thus, the variation in resistivity between rollers was significant even when the rollers were made using the same formulation from the same batch. Variations in resistivity within each roller were also found to be significant, with variations as high as 600% between regions of low and high resistivity within the same roller. The variations within each roller either resulted in rollers that failed to print or that produced poor quality images due to inconsistencies in ink transfer arising from the variations in resistivities within the roller.
In this example, developer rollers were produced with the formulation shown in Table 2 with a carbon black loadings exceeding the percolation limit. The rollers were prepared as described in relation to Example 1. The resistivity of rollers from this process was measured to have specific resistivities of 8-24 KΩ·cm. The variation in resistivity between rollers from the same batch was significantly less than in Example 1.
In this example, surfaces of steel rollers were roughened by sand blasting for better adhesion. Mixtures of fine powders of alumina and titania in the ratio shown in Table 3 were applied on roller surfaces with a plasma spray gun. Coating thickness was controlled by process parameters such as powder feeding rate or coating time. Shafts were masked during the process to maintain their critical dimensions and good electrical contact. Rollers were further processed by grinding after coating to meet the dimensional and surface roughness requirements. The specific resistivities of the coatings ranged from 3×106 Ohm·cm to 4×107 Ohm·cm.
A binary ink development unit was built with a developer roller from Example 2 and uncoated metal secondary rollers (for both squeegee and cleaner roller). The BID was then tested on HP Indigo 7000 digital press. The printing trial was not successful because the printer could not calibrate the optical density of ink on media. A further investigation revealed the failure was due to power supply over-current due to the very low resistance at the nips between developer roller and secondary metal rollers. In this example, the nip current was 300 volts/1 kohms=0.33 A, which was beyond the power supply capacity.
Example 4 was repeated but the uncoated metal secondary rollers were replaced with the ceramic-coated roller B of Example 3 (see Table 3). The BID still failed colour calibration due to over current at nominal voltages, but successfully printed when reducing the electrical bias between developer roller and secondary rollers from 325 volts to 250 volts.
Example 4 was repeated but the uncoated metal secondary rollers were replaced with the ceramic-coated roller C of Example 3 (see Table 3). This BID successfully printed with nominal printing conditions without any errors.
A developer roller formed using a nitrile rubber composition containing carbon black (specific resistivity of composition=5×104 Ohm·cm) was used in combination with an uncoated metal secondary roller. A 200 kΩ resistor was placed in series with metal secondary roller in order to increase the resistance of the secondary roller circuit.
A developer roller formed using a nitrile rubber composition containing carbon black (specific resistivity of composition=5×104 Ohm·cm) was used in combination with the ceramic-coated roller E of Example 3 (Table 3).
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/US2016/015128 | 1/27/2016 | WO | 00 |
| Publishing Document | Publishing Date | Country | Kind |
|---|---|---|---|
| WO2017/131666 | 8/3/2017 | WO | A |
| Number | Name | Date | Kind |
|---|---|---|---|
| 4142480 | Schwandt et al. | Mar 1979 | A |
| 4908665 | Takeda et al. | Mar 1990 | A |
| 5765084 | Asada | Jun 1998 | A |
| 5911099 | Nakajima et al. | Jun 1999 | A |
| 6256051 | Asada | Jul 2001 | B1 |
| 6451438 | Chiang et al. | Sep 2002 | B1 |
| 7172543 | Uesaka et al. | Feb 2007 | B2 |
| 7173805 | Lee | Feb 2007 | B2 |
| 7445588 | Hattori et al. | Nov 2008 | B2 |
| 7450892 | Tsubota | Nov 2008 | B2 |
| 7459254 | Yuasa et al. | Dec 2008 | B2 |
| 7505720 | Sugama | Mar 2009 | B2 |
| 7639973 | Sano et al. | Dec 2009 | B2 |
| 7981586 | Uchino et al. | Jul 2011 | B2 |
| 8079943 | Kim | Dec 2011 | B2 |
| 8090295 | Motokawa et al. | Jan 2012 | B2 |
| 8396403 | Breitenbach et al. | Mar 2013 | B2 |
| 8522438 | Gopalanarayanan et al. | Sep 2013 | B2 |
| 8626038 | Nelson et al. | Jan 2014 | B2 |
| 8918035 | Hasegawa et al. | Dec 2014 | B2 |
| 8968168 | Takeuchi et al. | Mar 2015 | B2 |
| 9046802 | Yoshida et al. | Jun 2015 | B2 |
| 20030097945 | Lee | May 2003 | A1 |
| 20040024166 | Hattori et al. | Feb 2004 | A1 |
| 20050118421 | Ashibe et al. | Jun 2005 | A1 |
| 20060019101 | Lee | Jan 2006 | A1 |
| 20060165448 | Yoshinaga | Jul 2006 | A1 |
| 20070107225 | Kim | May 2007 | A1 |
| 20080159791 | Urano et al. | Jul 2008 | A1 |
| 20090290909 | Nagami et al. | Nov 2009 | A1 |
| 20100155677 | Beach et al. | Jun 2010 | A1 |
| 20100209156 | Raz | Aug 2010 | A1 |
| 20110158705 | Kim et al. | Jun 2011 | A1 |
| 20110170909 | Garcia | Jul 2011 | A1 |
| 20110177926 | Kusano et al. | Jul 2011 | A1 |
| 20110206416 | Berg | Aug 2011 | A1 |
| 20120014723 | Mizumoto | Jan 2012 | A1 |
| 20130315620 | Kikuchi et al. | Nov 2013 | A1 |
| 20150227074 | Ito et al. | Aug 2015 | A1 |
| 20150331340 | Nishioka et al. | Nov 2015 | A1 |
| Number | Date | Country |
|---|---|---|
| 104448778 | Mar 2015 | CN |
| 07160062 | Jun 1995 | JP |
| 10231419 | Sep 1998 | JP |
| 2000026719 | Jan 2000 | JP |
| 2000029319 | Jan 2000 | JP |
| 2003202722 | Jul 2003 | JP |
| 2003248373 | Sep 2003 | JP |
| 2005220317 | Aug 2005 | JP |
| 2006201564 | Aug 2006 | JP |
| 2007279679 | Oct 2007 | JP |
| 2008033248 | Feb 2008 | JP |
| 2008157980 | Jul 2008 | JP |
| 2009204875 | Sep 2009 | JP |
| 2010018811 | Jan 2010 | JP |
| 2010134255 | Jun 2010 | JP |
| 2010237445 | Oct 2010 | JP |
| 2011053658 | Mar 2011 | JP |
| 2012042880 | Mar 2012 | JP |
| 2012107134 | Jun 2012 | JP |
| 2013015716 | Jan 2013 | JP |
| 2013134369 | Jul 2013 | JP |
| 2014133853 | Jul 2014 | JP |
| 2014209177 | Nov 2014 | JP |
| 2015219365 | Dec 2015 | JP |
| 2015219375 | Dec 2015 | JP |
| 2015232704 | Dec 2015 | JP |
| 2015232705 | Dec 2015 | JP |
| WO-2010039134 | Apr 2010 | WO |
| WO-2011009732 | Jan 2011 | WO |
| WO-2012098590 | Jul 2012 | WO |
| WO-2013151562 | Oct 2013 | WO |
| WO-2015116206 | Aug 2015 | WO |
| Entry |
|---|
| International Search Report and Written Opinion for International Application No. PCT/US2016/015128 dated Oct. 26, 2016, 9 pages. |
| Number | Date | Country | |
|---|---|---|---|
| 20180321618 A1 | Nov 2018 | US |
