EP3653386B1 - Inkjet head, inkjet recording device and method for producing an inkjet head - Google Patents
Inkjet head, inkjet recording device and method for producing an inkjet head Download PDFInfo
- Publication number
- EP3653386B1 EP3653386B1 EP18831247.4A EP18831247A EP3653386B1 EP 3653386 B1 EP3653386 B1 EP 3653386B1 EP 18831247 A EP18831247 A EP 18831247A EP 3653386 B1 EP3653386 B1 EP 3653386B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- liquid
- repellent
- film
- layer
- inkjet head
- 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.)
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Images
Classifications
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- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41J—TYPEWRITERS; SELECTIVE PRINTING MECHANISMS, i.e. MECHANISMS PRINTING OTHERWISE THAN FROM A FORME; CORRECTION OF TYPOGRAPHICAL ERRORS
- B41J2/00—Typewriters or selective printing mechanisms characterised by the printing or marking process for which they are designed
- B41J2/005—Typewriters or selective printing mechanisms characterised by the printing or marking process for which they are designed characterised by bringing liquid or particles selectively into contact with a printing material
- B41J2/01—Ink jet
- B41J2/135—Nozzles
- B41J2/16—Production of nozzles
- B41J2/1621—Manufacturing processes
- B41J2/1626—Manufacturing processes etching
- B41J2/1629—Manufacturing processes etching wet etching
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41J—TYPEWRITERS; SELECTIVE PRINTING MECHANISMS, i.e. MECHANISMS PRINTING OTHERWISE THAN FROM A FORME; CORRECTION OF TYPOGRAPHICAL ERRORS
- B41J2/00—Typewriters or selective printing mechanisms characterised by the printing or marking process for which they are designed
- B41J2/005—Typewriters or selective printing mechanisms characterised by the printing or marking process for which they are designed characterised by bringing liquid or particles selectively into contact with a printing material
- B41J2/01—Ink jet
- B41J2/135—Nozzles
- B41J2/16—Production of nozzles
- B41J2/1621—Manufacturing processes
- B41J2/1631—Manufacturing processes photolithography
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41J—TYPEWRITERS; SELECTIVE PRINTING MECHANISMS, i.e. MECHANISMS PRINTING OTHERWISE THAN FROM A FORME; CORRECTION OF TYPOGRAPHICAL ERRORS
- B41J2/00—Typewriters or selective printing mechanisms characterised by the printing or marking process for which they are designed
- B41J2/005—Typewriters or selective printing mechanisms characterised by the printing or marking process for which they are designed characterised by bringing liquid or particles selectively into contact with a printing material
- B41J2/01—Ink jet
- B41J2/135—Nozzles
- B41J2/16—Production of nozzles
- B41J2/1621—Manufacturing processes
- B41J2/1632—Manufacturing processes machining
- B41J2/1634—Manufacturing processes machining laser machining
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41J—TYPEWRITERS; SELECTIVE PRINTING MECHANISMS, i.e. MECHANISMS PRINTING OTHERWISE THAN FROM A FORME; CORRECTION OF TYPOGRAPHICAL ERRORS
- B41J2/00—Typewriters or selective printing mechanisms characterised by the printing or marking process for which they are designed
- B41J2/005—Typewriters or selective printing mechanisms characterised by the printing or marking process for which they are designed characterised by bringing liquid or particles selectively into contact with a printing material
- B41J2/01—Ink jet
- B41J2/135—Nozzles
- B41J2/16—Production of nozzles
- B41J2/1621—Manufacturing processes
- B41J2/164—Manufacturing processes thin film formation
- B41J2/1642—Manufacturing processes thin film formation thin film formation by CVD [chemical vapor deposition]
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41J—TYPEWRITERS; SELECTIVE PRINTING MECHANISMS, i.e. MECHANISMS PRINTING OTHERWISE THAN FROM A FORME; CORRECTION OF TYPOGRAPHICAL ERRORS
- B41J2/00—Typewriters or selective printing mechanisms characterised by the printing or marking process for which they are designed
- B41J2/005—Typewriters or selective printing mechanisms characterised by the printing or marking process for which they are designed characterised by bringing liquid or particles selectively into contact with a printing material
- B41J2/01—Ink jet
- B41J2/135—Nozzles
- B41J2/16—Production of nozzles
- B41J2/1621—Manufacturing processes
- B41J2/164—Manufacturing processes thin film formation
- B41J2/1646—Manufacturing processes thin film formation thin film formation by sputtering
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41J—TYPEWRITERS; SELECTIVE PRINTING MECHANISMS, i.e. MECHANISMS PRINTING OTHERWISE THAN FROM A FORME; CORRECTION OF TYPOGRAPHICAL ERRORS
- B41J2/00—Typewriters or selective printing mechanisms characterised by the printing or marking process for which they are designed
- B41J2/005—Typewriters or selective printing mechanisms characterised by the printing or marking process for which they are designed characterised by bringing liquid or particles selectively into contact with a printing material
- B41J2/01—Ink jet
- B41J2/135—Nozzles
- B41J2/165—Prevention or detection of nozzle clogging, e.g. cleaning, capping or moistening for nozzles
Definitions
- the present invention relates to an inkjet head, an inkjet recording device, and a method for producing an inkjet head.
- inkjet recording device inkjet printer
- inkjet recording device ejects (discharges) ink droplets from nozzles of inkjet heads, thereby forming an image on a recording medium.
- inkjet recording device ejects ink droplets
- ink may adhere to nozzle surfaces (around the openings of the nozzles on the ejection side) of the inkjet heads owing to the influence of ink mist generated in the printer or ink bounced by the recording medium.
- ink adhering to the nozzle surfaces affects ejection angles of ink droplets when the ink droplets are ejected from the nozzles and changes the ejection angles.
- an ink-repellent layer on nozzle surfaces by coating the nozzle surfaces with an ink-repellent agent.
- the ink-repellent layer there is known a film formed by bonding organic functional groups containing fluorine through dehydration-condensation reactions with silane coupling ([-OH] + [HO-Si-R-F] ⁇ [H 2 O] + [-O-Si-R-F]) (see Patent Literature 1).
- Silanol groups in the compound of the silane coupling agent and hydroxy groups on the surface of a base film form siloxane bonds. It is desirable that the base film have a strong covalent bonding property. It is known that a base film having a strong ionic bonding property does not form siloxane bonds (see Non-Patent literature 1).
- a nozzle substrate that has inner walls of nozzle holes and a plurality of layers of ink resistant protective films (see Patent Literature 2).
- a thermal oxide film having a high coating property is formed.
- a metal oxide having ink resistance is formed on the inner walls, the front surface, and the back surface by a CVD (Chemical Vapor Deposition) method, and then a water-repellent film is formed on the ejection surface side.
- a metal oxide such as tantalum pentoxide, hafnium oxide, niobium oxide, titanium oxide, or zirconium oxide, is used. This is because these metal oxides are highly resistant to alkaline ink (discharging liquid).
- the water-repellent film preferably contains a fluorine-containing organosilicon compound as a main component. This is because hydroxy groups on the surface of the ink-resistant protective film firmly bond with hydrolyzing groups, such as methoxy groups, of the fluorine-containing organosilicon compound, so that adhesion between the ink-resistant protective film and the water-repellent film formed on the surface of the ink-resistant protective film is improved.
- Patent Literature 3 discloses an inkjet head according to the preamble of claim 1 and a method for producing an inkjet head according to the preamble of claim 7.
- metal elements that may be contained in a metal oxide film used as a protective film such as tantalum pentoxide, hafnium oxide, niobium oxide, titanium oxide, and zirconium oxide, are transition metal elements in the group 4 or the group 5. It is known that these metal elements in their oxidation states are highly stable and their outermost shell orbitals are filled with electrons and their internal orbitals are unfilled. That is, the bonding of these metal oxide films has a strong ionic bonding property compared with the bonding of oxide films made of typical elements, such as SiO 2 , as shown in the table I. This leads to low reactivity to the silane coupling agent (liquid-repellent agent, water-repellent agent).
- silane coupling agent liquid-repellent agent, water-repellent agent
- liquid repellency water repellency, ink repellency
- Objects of the present invention include improving reactivity with the liquid-repellent agent and resistance to ink of the nozzle substrate on the ejection surface side, thereby preventing decrease in liquid repellency of the nozzle substrate on the ejection surface side.
- the present invention can improve reactivity with the liquid-repellent agent and resistance to ink of the nozzle substrate on the ejection surface side, and prevent decrease in liquid repellency of the nozzle substrate on the ejection surface side.
- FIG. 1 is a schematic view of configuration of the inkjet recording device 1 of this embodiment viewed from the front.
- the inkjet recording device 1 includes a medium supplying unit 10, an image forming unit 20, a medium receiving unit 30, and a controller (not illustrated).
- recording media R stored in the medium supplying unit 10 are conveyed to the image forming unit 20 in accordance with control operation performed by the controller, and, after images are formed, discharged to the medium receiving unit 30.
- the medium supplying unit 10 includes a medium supplying tray 11 and a conveying unit 12.
- the medium supplying tray 11 is a plate-shaped member provided so as to be able to store one or more recording media R.
- the medium supplying tray 11 moves up and down according to the amount of recording media R, and the top recording medium R among the recording media R stored thereon is placed at the conveyance start position of the conveying unit 12.
- recording media R various types of recording media that can be held to be curved on the outer circumferential surface of an image forming drum 21, such as printing paper, cellophane, films and fabrics having various thicknesses, are used.
- the conveying unit 12 includes a plurality of (for example, two) rollers 121, 122, a ring-shaped belt 123 supported by the rollers 121, 122 on the inner circumferential surface, and a supplying unit (not illustrated) that delivers the top recording medium R among the recording media R stored on the medium supplying tray 11 to the belt 123.
- the conveying unit 12 conveys and sends the recording medium R, which has been delivered onto the belt 123 by the supplying unit, to the image forming unit 20.
- the image forming unit 20 includes the image forming drum 21, a first delivering unit 22, a temperature measuring unit 23, head units 24, a heating unit 25, a second delivering unit 26, and cleaning units 27 (see FIGS. 3A and 3B ).
- the image forming drum 21 has a cylindrical outer circumferential surface.
- the image forming drum 21 holds the recording medium R on the outer circumferential surface (conveying surface) and conveys the recording medium R along a conveying path according to rotating operation of the image forming drum 21.
- a heater is provided on the inner surface side of the image forming drum 21, . The heater can heat the conveying surface so that the recording medium R placed on the conveying surface has a predetermined temperature.
- the first delivering unit 22 delivers the recording medium R delivered by the conveying unit 12 to the image forming drum 21.
- the first delivering unit 22 is provided at a position between the conveying unit 12 of the medium supplying unit 10 and the image forming drum 21.
- the first delivering unit 22 includes a claw part(s) 221 that grips one end of the recording medium R conveyed by the conveying unit 12 and a cylindrical delivering drum 222 that leads the recording medium R gripped by the claw part 221.
- the recording medium R that the claw part 221 has received from the conveying unit 12 is sent to the delivering drum 222, moves along the outer circumferential surface of the rotating delivering drum 222, and is led to and delivered to the outer circumferential surface of the image forming drum 21.
- the temperature measuring unit 23 is provided at a position between the point where the recording medium R is placed on the conveying surface of the image forming drum 21 and the point where the recording medium R faces an ink ejection surface (jetting surface) of a head unit 24 that the recording medium R faces first.
- the temperature measuring unit 23 measures temperature of a surface of the recording medium R (temperature of the surface opposite to the surface contacting the conveying surface) being conveyed.
- a radiation thermometer is used, for example.
- the radiation thermometer measures the surface temperature of the recording medium R, which does not contact the temperature measuring unit 23 (radiation thermometer), by measuring intensity distribution of infrared rays.
- the temperature measuring unit 23 has a plurality of sensors arranged along a width direction perpendicular to the direction in which the recording medium R is conveyed in the image forming unit 20 (conveying direction), the width direction being perpendicular to the surface of FIG. 1 , so as to be able to measure temperature at a plurality of points.
- Each measurement data is output to the controller at an appropriate predetermined timing to be controlled.
- each of the head units 24 ejects (discharges) ink droplets at positions on the recording medium R from a plurality of nozzle opening parts (nozzle holes) formed on the ink ejection surface that faces the recording medium R, thereby forming an image.
- the inkjet recording device 1 in this embodiment has four head units 24 that are arranged a predetermined distance away from the outer circumferential surface of the image forming drum 21 and at predetermined intervals from one another.
- the four head units 24 output ink of four colors: C (Cyan), M (Magenta), Y (Yellow), and K (Black), respectively.
- the C, M, Y, and K inks are ejected in this order from the upstream side in the conveying direction of the recording medium R.
- a normal liquid ink is herein used.
- the ink fixes to the recording medium R when ink evaporates and dries by the operation of the heating unit 25.
- Each of the head units 24 has a line scan head that is capable of forming an image over an image forming width on the recording medium R in combination with the rotation of the image forming drum 21.
- the heating unit 25 heats the surface of the recording medium R being conveyed.
- the heating unit 25 heats the recording medium R by generating heat with an electric heating wire being energized and heating the air, or by emitting infrared rays.
- the heating unit 25 is provided at a position close to the outer circumferential surface of the image forming drum 21 so as to be able to heat the recording medium R until the image forming drum 21 delivers the recording medium R to the second delivering unit 26 after the head units 24 eject ink onto the recording medium R conveyed by the rotation of the image forming drum 21.
- the operation of the heating unit 25 dries the ink ejected from the nozzles of the head units 24 and fixes the ink to the recording medium R.
- the second delivering unit 26 conveys the recording medium R on which the ink has been ejected and fixed from the image forming drum 21 to the medium receiving unit 30.
- the second delivering unit 26 includes a plurality of (for example, two) rollers 261, 262, a ring-shaped belt 263 supported by the rollers 261, 262 on the inner side surface, and a cylindrical delivery roller 264.
- the second delivering unit 26 leads the recording medium R on the image forming drum 21 onto the belt 263 with the delivery roller 264, moves the recording medium R, which is received, together with the belt 263 that circulates in accordance with the rotation of the rollers 261, 262, and conveys the recording medium R to the medium receiving unit 30.
- the cleaning units 27 perform cleaning operation of the ink ejection surfaces of the head units 24.
- the cleaning units 27 are each provided adjacent to the image forming drum 21 in the width direction. When the head units 24 move in the width direction, the ink ejection surfaces of the head units 24 are set at the cleaning positions where the cleaning units 27 perform cleaning.
- the medium receiving unit 30 stores the recording medium R sent from the image forming unit 20 after image formation until a user takes out the recording medium R.
- the medium receiving unit 30 includes a plate-shaped medium receiving tray 31 on which the recording medium R conveyed by the second delivering unit 26 is stored.
- FIGS. 2A and 2B are illustrations showing configuration of the head unit 24.
- FIG. 2A is a schematic structural view of the head unit 24 located above the conveying surface of the image forming drum 21 viewed from the upstream side in the conveying direction of the recording medium R.
- FIG. 2B is a bottom view of the head unit 24 viewed from the conveying surface side of the image forming drum 21.
- the head unit 24 has a plurality of inkjet heads 241.
- one head unit 24 has 16 inkjet heads 241, although the present invention is not limited to this.
- the 16 inkjet heads 241 make eight sets of inkjet modules 242, wherein a pair of inkjet heads 241 are included in one inkjet module 242.
- the inkjet modules 242 are fixed to a fixing member 245 so as to be staggered in appropriate relative positions.
- the fixing member 245 is supported and held by a carriage 246.
- the carriage 246 also holds a first sub-tank 243 and second sub-tanks 244 to feed ink to the inkjet heads 241.
- the carriages 246 of the respective four head units 24 are individually movable in the width direction over the image forming drum 21.
- each of the inkjet heads 241 has a plurality of nozzles 2411.
- the inkjet head 241 ejects ink (droplets) from opening parts (nozzle holes) of nozzles 2411 formed on the bottom surface of the inkjet head 241 (nozzle opening surface 241a), so that the ink droplets land on the recording medium R held on the conveying surface of the image forming drum 21.
- each of the inkjet heads 241 shown here has the opening parts of the nozzles 2411 arranged in two rows in the conveying direction in a two-dimensional array pattern, the present invention is not limited to this.
- the opening parts of the nozzles 2411 may be arranged in an appropriate one-dimensional or two-dimensional array pattern.
- the arrangement range of these opening parts of all the 16 inkjet heads 241 covers, in the width direction, the recordable width of the recording medium R held on the conveying surface. This enables one-pass image forming with the head units 24 fixed.
- the nozzle opening surfaces 241a of the 16 inkjet heads 241 are covered with a liquid-repellent layer 43 (water-repellent layer, ink-repellent layer) (see FIG. 5 ).
- FIGS. 3A and 3B are illustrations to explain configuration of the cleaning unit 27.
- FIG. 3A is a perspective view of the image forming drum 21.
- FIG. 3B is a view behind the image forming drum 21 viewed from the same front side as FIG. 1 , wherein the image forming drum 21 is seen through.
- the cleaning unit 27 wipes off ink and other impurities (collectively called foreign elements) adhering to the nozzle opening surfaces 241a of the inkjet heads 241, thereby removing them after ink is ejected for image formation and/or maintenance is performed. As shown in FIG. 3A , the cleaning unit 27 is arranged next to the image forming drum 21 in the width direction so that the ink ejection surface can be cleaned when the head unit 24 moves in the width direction.
- the cleaning unit 27 includes a wiping member 271, an elastic member 272, an unwinding roller 273, and a winding roller 274.
- this configuration is provided to each of the head units 24, the configuration may be shared by the head units 24 by making the cleaning unit 27 movable in the conveying direction.
- the wiping member 271 is a long cloth-like sheet member of which length (width) in the width direction can cover the ink ejection surface (at least all the nozzle opening surfaces 241a).
- a desirable member as the wiping member 271 is the one that easily absorbs moisture of ink, has lower hardness than the hardness of the material of the ink ejection surface, and hardly damages the liquid-repellent layer. Examples of such a member include polyester, acrylic, polyamide, and polyurethane that can form a woven or non-woven fabric.
- a member that has a high water-absorbing property and can easily absorb liquid with a low pressing force at the time of contact is further preferable.
- the wiping member 271 may have a blade-like structure.
- the elastic member 272 faces the ink ejection surface with the wiping member 271 in between.
- the surface (pressing surface) of the elastic member 272 facing the ink ejection surface has a size that can cover the entire ink ejection surface.
- the elastic member 272 is movable approximately perpendicular to the ink ejection surface.
- materials that do not damage nozzles when pressed against the nozzle opening surfaces 241a such as a sponge (foamed resin) and rubber, are used.
- the wiping member 271 contacts the nozzle opening surfaces 241a (ink ejection surface) in a state of being approximately parallel to the nozzle opening surfaces 241a as a whole by being moved in a direction to approach the nozzle opening surfaces 241a.
- the relative positions (distance) of the elastic member 272 and the ink ejection surface when the wiping member 271 contacts the nozzle opening surfaces 241a are fixed. This makes the pressing force of the wiping member 271 against the ink ejection surface the same every time within a range of effects of the liquid-repellent layer that peels off from the surface of the nozzle opening surfaces 241a.
- the relative positions of the elastic member 272 and the ink ejection surface are determined so as to have an appropriate level of the pressing force for cleaning the ink on the ink ejection surface.
- the pressing force may be variable. In such a case, the maximum value of the pressing force is determined according to a relationship between the surface shape of the nozzle opening surfaces 241a and the wiping member 271, as described later.
- the wiping member 271 is unwound from the unwinding roller 273 and wound up by the winding roller 274 in accordance with winding operation performed by the winding roller 274. During this time, the elastic member 272 presses the wiping member 271 against the ink ejection surface approximately uniformly. This makes the clean (with no ink adhered) wiping member 271 contact the ink ejection surface and clean ink or the like adhering to the nozzle opening surfaces 241a (ink ejection surface). If the whole wiping member 271 is unwound from the unwinding roller 273, the wiping member 271 can be replaced easily.
- FIG. 4 is a schematic view of a cross-sectional shape of the inkjet head 241.
- the inkjet heads 241 is a bend-mode inkjet head that is formed with a plurality of plates (substrates) layered as shown in FIG. 4 . More specifically, each of the inkjet heads 241 includes the nozzle substrate 40A, a pressure chamber substrate 50, an oscillating plate 60, a spacer substrate 70, and a wiring substrate 80 layered in this order from the side where the nozzle opening surface 241a (ink ejection surface, lower side) are provided to the upper side.
- the pressure chamber 51 abuts the piezoelectric element part 71 of the spacer substrate 70 with the oscillating plate 60 in between, and electrically connects to the nozzle 2411.
- a control signal from the controller of the inkjet recording device 1 is input to the piezoelectric element part 71 through a wire(s) of the wiring substrate 80, the piezoelectric element part 71 physically oscillates.
- an intermediate substrate having a flow channel that connects the pressure chamber 51 and the nozzle 2411.
- FIG. 5 is a schematic cross-sectional view of the nozzle substrate 40A.
- the lower part of the drawing is referred to as the (ink) ejection surface side (extemal side of the head), and the upper part of the drawing is referred to as the flow channel side (internal side of the head, pressure chamber side).
- the nozzle substrate 40A includes a base part 41, a liquid-repellent-layer base film 42A, and a liquid-repellent layer 43.
- a material of the base part 41 include silicon; metal, such as SUS (Steel Use Stainless), nickel, and metal containing nickel; and resin, such as polyimide.
- silicon is used as the base
- processes such as photolithography used in semiconductor processing, can be performed for nozzle processing.
- Using such a process enables highly precise nozzle processing and production of inkjet heads having few variations in ejection angles and high quality in image depiction.
- the nozzle 2411 is an ink nozzle formed in the base part 41, and includes an ink flow channel and a nozzle hole on the ejection surface side.
- the liquid-repellent-layer base film 42A is provided on the ejection surface side, where the cleaning unit 27 wipes off ink during maintenance of the base part 41, and is the base layer of the liquid-repellent layer 43 on the flow channel side (base part 41 side).
- the material of the liquid-repellent-layer base film 42A is silicon carboxide (silicon carboxide film) Si a C b O c (a, b, c: the number of atoms).
- the liquid-repellent layer 43 is provided on the ejection surface side of the liquid-repellent-layer base film 42A, and has, for example, a structure having perfluorocarbon chains and has ink-repellent properties (water repellency, ink repellency).
- the silicon carboxide film is selected as the liquid-repellent-layer base film 42A in this embodiment.
- the silicon carboxide film can achieve alkali resistance, chemical mechanical polishing (CMP) resistance, and fixability of the liquid-repellent agent (siloxane bonds can be formed).
- CMP chemical mechanical polishing
- the chemical mechanical polishing resistance is resistance to film reduction of the liquid-repellent-layer base film due to ink wiping by the cleaning unit 27.
- ink on an ejection surface of a nozzle substrate is wiped off with a cloth or the like of a cleaning unit.
- Silicon carbide SiC ranks second to DLC (diamond-like carbon) in hardness and is known as a material that is hardly alkali-etched.
- Use of a silicon carboxide film that is produced by introducing carbon into silicon oxide as the liquid-repellent-layer base film 42A makes it possible to improve its alkali resistance as well as to maintain reactivity thereof with the silane coupling agent on the nozzle surface.
- Inkjet printing has been aggressively used in the textile field recently. In comparison with the conventional textile printing methods, the inkjet printing has merits of: requiring no plates to be generated; being applicable to small lot production; and having less ink waste.
- an aqueous ink such as a disperse dye ink or a sublimation dye ink
- an additive to the ink such as a dispersant
- dispersion of the pigment molecules is controlled with pH of the ink.
- the conventional liquid-repellent layer formed by silane coupling has low reliability because, in an alkaline environment, hydrolysis of the liquid-repellent layer is accelerated or desorption of the liquid-repellent material is accelerated by the etching of the liquid-repellent-layer base film. Even if textile-printing ink itself is neutral or slightly alkaline, a fabric coated with an alkaline pretreatment agent may be used to improve color development. In an inkjet printer for textile printing, the alkaline pretreatment agent on the fabric surface may affect reliability of liquid repellency of the surface of the subsequent inkjet head owing to raising treatment or the like.
- the silicon carboxide film has high chemical stability and can improve alkali resistance.
- FIGS. 6A and 6B the composition ratio of the silicon carboxide film Si a C b O c having high alkali resistance is described.
- FIG. 6A is a diagram showing a preferable range of the composition ratio of the silicon carboxide film in a triangular diagram showing the ratio of Si, C, and O in the number of atoms.
- FIG. 6B is a diagram showing a coordinate point P0 in the triangular diagram showing the ratio of Si:C:O in the number of atoms.
- the composition ratio (ratio in the number of atoms) of silicon Si, carbon C, and oxygen O of the silicon carboxide film is shown in the triangular diagram that is an equilateral triangle having three vertexes corresponding to Si only, C only, and O only, respectively.
- the vertexes corresponding to only Si, C, and O are referred to as VSi, VC, and VO, respectively.
- the coordinates thereof are represented by a length ⁇ on the side from vertex VO to vertex VSi, a length ⁇ on the side from vertex VSi to vertex VC, and a length ⁇ on the side from vertex VSi to vertex VO.
- ⁇ b / a + b + c
- ⁇ c / a + b + c
- the preferable composition ratio of a:b:c of the silicon carboxide film Si a C b O c as the liquid-repellent-layer base film 42A is described.
- lines L1 to L6 on the triangular diagram showing composition of Si, C, and O are described.
- the coordinate point corresponding to silicon dioxide SiO 2 is PSiO 2
- the coordinate point corresponding to silicon carbide SiC is PSiC (P1)
- the coordinate point corresponding to silicon dicarbide SiC 2 is PSiC 2 (P4).
- the line L1 is a line segment connecting the coordinate point PSiO 2 and the coordinate point P1, and composite elements on the line L1 are SiC 1-t O 2t (0 ⁇ t ⁇ 1).
- the line L2 is a line segment connecting the coordinate point PSiO 2 and the coordinate point P4, and composite elements on the line L2 are SiC 2(1-s) O 2s (0 ⁇ s ⁇ 1).
- the line L3 is a line segment connecting the coordinate point PSiO 2 and the vertex VC.
- the proportion of carbon be higher than the proportion of oxygen (c ⁇ b).
- the liquid-repellent-layer base film 42A at least needs to contain oxygen (c > 0) because hydroxy groups that react with a silane coupling agent as a liquid-repellent agent need to be present on the surface of the liquid-repellent-layer base film 42A when the liquid-repellent layer 43 is formed. Therefore, it is preferable that the ratio of carbon: oxygen (c/b) satisfy 0 ⁇ c/b ⁇ 1.
- silicon oxide silicon monoxide SiO and silicon dioxide SiO 2 are known.
- Amorphous silicon oxide having an intermediate composition namely SiO x where x ⁇ 2 stoichiometrically, also exists metastably.
- SiO x that satisfies 2 ⁇ x does not exist as a film because it is so-called peroxide and is unstable.
- hydroxy groups which react with the silane coupling agent, need to exist on the surface of the liquid-repellent-layer base film 42A when the liquid-repellent layer 43 is formed, the film at least needs to contain oxygen. Therefore, it is preferable that the ratio of silicon: oxygen (c/a) satisfy 0 ⁇ c/a ⁇ 2.
- the proportion of carbon be larger than the line L1, and the proportion of silicon be larger than the line L2. Because silicon and carbon are both group 14 elements and have the same valence, substitution in the compound is possible. In terms of alkali resistance and chemical mechanical polishing resistance, it is preferable that the proportion of silicon and the proportion of carbon be around the same, or the proportion of carbon be larger than the proportion of silicon (1 ⁇ b/a).
- the distance of a covalent bond formed by sp hybridized orbitals of a carbon atom is shorter than that of a covalent bond formed by sp hybridized orbitals of a silicon atom because the sp hybridized orbitals of a carbon atom are formed from 2s and 2p orbitals, whereas these of a silicon atom are formed from 3s and 3p orbitals.
- the proportion of carbon being too high decreases adhesion between the base part 41 and the liquid-repellent-layer base film 42A owing to the film stress of the liquid-repellent-layer base film 42A being larger.
- the proportion of carbon needs to be limited (b/a ⁇ 2). In consideration of this, the inventors believe it is preferable that the proportion of carbon be larger than the line L1 and the proportion of silicon be larger than the line L2.
- FIG. 7 is a flowchart showing a first nozzle substrate producing process.
- FIG. 8A is a schematic cross-sectional view of the base part 41 before nozzle processing.
- FIG. 8B is a schematic cross-sectional view of the base part 41 with the liquid-repellent-layer base film 42A formed.
- FIG. 8C is a schematic cross-sectional view of the base part 41 with the liquid-repellent layer 43 formed.
- FIG. 8D is a schematic cross-sectional view of the base part 41 with the protective sheet 45 attached.
- FIG. 8E is a schematic cross-sectional view of the base part 41 with nozzles 2411 formed.
- FIG. 8F is a schematic cross-sectional view of the nozzle substrate 40A with the protective sheet 45 removed.
- the first nozzle substrate producing process for producing the nozzle substrate 40A is described.
- a manufacturer prepares a base part 41 as a base member as shown in FIG. 8A (Step ST11).
- the base part 41 is a polyimide (PI) film.
- the material of the base part 41 can be resin, such as PET (PolyEthylene Terephthalate) or PPS (PolyPhenylene Sulfide). More specifically, Kapton film manufactured by DuPont, Upilex 75S manufactured by Ube Industries, TORELINA manufactured by TORAY, or the like may be used.
- Polyimide has high heat resistance, which enables annealing at a high temperature after the liquid-repellent-layer base film 42A is formed or after the liquid-repellent layer 43 is formed.
- PPS has high dimensional stability and can reduce variation in the length of nozzle rows of the inkjet heads 241.
- the manufacturer forms a silicon carboxide film having a composition ratio in the preferable range shown in FIG. 6A on the ejection surface side of the base part 41 prepared in Step ST11, thereby forming the liquid-repellent-layer base film 42A (Step ST12).
- Use of the silicon carboxide film can produce the liquid-repellent-layer base film 42A having high alkali resistance and chemical mechanical polishing resistance. Because siloxane bonds can be formed, the liquid-repellent-layer base film 42A can have high fixability with the liquid-repellent agent.
- the silicon carboxide film can be formed using the following film-forming methods or the like.
- plasma treatment may be performed on the base part 41.
- the plasma treatment can be performed with oxygen gas, argon gas, or a mixture of these gases. Performing the plasma treatment can bring about effects of decontaminating or activating the surface of the base part 41 and improve adhesion between the liquid-repellent-layer base film 42A and the base part 41.
- reverse sputtering treatment may be performed on the base part 41.
- sputtering is performed on the base part 41 using oxygen gas, argon gas, or a mixture of these gases. Performing the reverse sputtering treatment can bring about effects of decontaminating or activating the surface of the base part 41 and improve adhesion between the liquid-repellent-layer base film 42A and the base part 41.
- the material gas may be hydrogenated.
- the hydrogenation may improve the stress, the film hardness, and the abrasion resistance of the silicon carboxide film.
- the liquid-repellent-layer base film 42A may be formed by firstly forming a silicon oxide film or a silicon carboxide film and secondly introducing carbon to the film surface thereof.
- carbon introduction plasma treatment with hydrocarbon gas, such as methane or ethane, can be used.
- hydrocarbon gas such as methane or ethane
- carbon introduction an ion implantation method, an ion shower doping method, or the like can be used.
- the composition ratio of the surface of the liquid-repellent-layer base film (outermost layer) can be controlled by carbonization to be a desirable composition ratio (within the preferable range shown in FIG. 6A ).
- Step ST12 in order to further improve fixability between the silicon carboxide film and the liquid-repellent agent, additional treatment, such as oxidation treatment during or after the film formation, may be performed so as to increase the number of siloxane bonding sites (-OH groups) on the surface of the silicon carboxide film.
- additional treatment include: oxygenating the silicon carboxide film as the liquid-repellent-layer base film 42A during the film formation thereof; and, after forming a silicon carbide film or the silicon carboxide film, oxidizing the surface thereof through oxygen plasma treatment or the like.
- the silicon carboxide film in Step ST12 be amorphous or monocrystalline. If the film is polycrystalline, the film may be selectively etched at crystal grain boundaries as etching sites and thereby have pinholes formed when immersed in an alkaline solution, and even the base material below may be etched. On the other hand, if the film is amorphous or monocrystalline, the film is not selectively etched even when immersed in the alkaline solution because there are no crystal grain boundaries as etching sites, so that the liquid-repellent-layer base film (flow channel protective film on the inner wall of nozzles) has higher alkali resistance.
- the manufacturer forms the liquid-repellent layer 43 on the ejection surface side (front surface) of the liquid-repellent-layer base film 42A formed in Step ST12 (Step ST13).
- the liquid-repellent layer 43 may be formed by application or deposition of a silane coupling agent as the liquid-repellent agent having perfluoro carbon chains.
- a silane coupling agent OPTOOL manufactured by Daikin Industries, WR4 manufactured by Merck, FG-5080 and FG-5010 manufactured by FluoroTechnology, or the like may be used.
- the formation of the liquid-repellent-layer base film 42A in Step ST12 and the formation of the liquid-repellent layer 43 in Step ST13 be performed continuously without exposure thereof to air atmosphere. Avoidance of exposure to air atmosphere makes it possible to avoid decrease in adhesion between the layers, change in film quality, and so forth due to contamination of the interfaces of the layers.
- plasma treatment may be performed.
- the plasma treatment can be performed with oxygen gas, argon gas, or a mixture of these gases. Performing the plasma treatment can bring about effects of decontaminating or activating the surface of the liquid-repellent-layer base film 42A, improve reactivity and adhesion of the liquid-repellent-layer base film 42A to the liquid-repellent layer 43, and improve alkali resistance and chemical mechanical polishing resistance.
- a primer layer may be formed before the liquid-repellent layer 43 is formed in Step ST13. The formation of the primer layer can improve adhesion between the liquid-repellent layer 43 and the liquid-repellent-layer base film 42A.
- the manufacturer attaches a protective sheet 45 to the ejection surface side (front surface) of the liquid-repellent layer 43 formed in Step ST13 (Step ST14).
- the protective sheet 45 has a base sheet 45a and an adhesive layer 45b on the base sheet 45a.
- As the base sheet 45a polyimide, PET, PPS, or the like can be used.
- the adhesive layer 45b is attached to the ejection surface side of the liquid-repellent layer 43.
- the manufacturer performs nozzle processing on the flow channel side (back surface) of the base part 41, the liquid-repellent-layer base film 42A, and the liquid-repellent layer 43 to which the protective sheet 45 is attached in Step ST14, thereby forming the nozzles 2411 (Step ST15).
- Step ST15 the manufacturer irradiates the back surface of the base part 41 with laser and forms the nozzles 2411.
- Use of the silicon carboxide film as the liquid-repellent-layer base film 42A makes it possible to accurately perform the laser processing on the liquid-repellent-layer base film 42A.
- the wavelength of the KrF excimer laser is 248 nm, that is, the photon energy is 5.0 eV.
- the band gap of the silicon carboxide film is narrower than that of SiO 2 owing to the effect of carbon introduction (the band gap of SiO 2 is 8-9 eV, and that of SiC is about 3 eV.). This improves absorption efficiency of a KrF excimer laser beam, allows the liquid-repellent-layer base film 42A to be ablated in nozzle processing, and restrains generation of burrs. Thus, processing accuracy of the edges of the nozzles 2411 is improved.
- the thickness of the liquid-repellent-layer base film 42A is preferably 100 nm or less, further preferably 50 nm or less, and still further preferably 20 nm or less. Laser ablation is performed easier on the liquid-repellent-layer base film 42A having a thinner film thickness, and less burrs are left.
- the adhesive strength between the protective sheet 45 and the surface of the liquid-repellent layer 43 should be between 0.1 and 0.7 N per 10 mm inclusive, and further preferably, between 0.15 and 0.64 N per 10 mm inclusive when the protective sheet 45 and the base part 41 are pulled apart in 180-degree opposite directions.
- Use of such an adhesive layer 45b makes it possible to perform nozzle processing without allowing the protective sheet 45 to peel off from the surface of the liquid-repellent layer 43 through handling of work in laser processing. This can restrain generation of burrs or the like.
- the base part 41 is made of metal material, such as SUS, and nozzle processing is performed using laser, it is preferable that a picosecond pulse laser be used as the laser light source.
- a picosecond pulse laser is used as the laser light source.
- the manufacturer removes the protective sheet 45 from the base part 41, the liquid-repellent-layer base film 42A, the liquid-repellent layer 43, and the protective sheet 45, in which the nozzles 2411 have been formed in Step ST15, thereby forming the nozzle substrate 40A (Step ST16), and ends the first nozzle substrate producing method.
- the adhesive strength between the protective sheet 45 and the surface of the liquid-repellent layer 43 should be between 0.1 and 0.7 N per 10 mm inclusive, or further preferably, between 0.15 and 0.64 N per 10 mm inclusive when the protective sheet 45 and the base part 41 are pulled apart in 180-degree opposite directions. Use of such an adhesive layer 45b makes it possible to remove the protective sheet 45 without applying a stress, which can cause distortion of the dimensions of the base part 41, to the base part 41.
- the manufacturer attaches the nozzle substrate 40A, which has been formed by the first nozzle substrate producing process, to the pressure chamber substrate 50 (or the intermediate substrate), and forms a substrate in which the nozzle substrate 40A, the pressure chamber substrate 50, the oscillating plate 60, the spacer substrate 70, and the wiring substrate 80 are layered.
- the manufacturer then connects the substrate with a driving circuit, an ink supply channel(s), and so forth, and forms the inkjet head 241.
- the inkjet head 241 is used as a part of the inkjet recording device 1.
- the inkjet head 241 includes the nozzle substrate 40A that includes: the base part 41 in which the nozzles 2411 that eject ink are formed; the liquid-repellent-layer base film 42A that is formed on the ejection surface side of the base part 41 and has the silicon carboxide film; and the liquid-repellent layer 43 that is formed on the ejection surface side of the liquid-repellent-layer base film 42A.
- the liquid-repellent-layer base film 42A as the silicon carboxide film makes it possible to improve reactivity with the liquid-repellent agent for forming the liquid-repellent layer 43 and resistance to ink, particularly alkaline ink, of the nozzle substrate 40A on the ejection surface side, thereby preventing decrease in liquid repellency of the nozzle substrate 40A on the ejection surface side.
- the liquid-repellent-layer base film 42A has the silicon carboxide film having a composition, in the triangular diagram showing the ratio of silicon Si, carbon C, and oxygen O in the number of atoms, within the range enclosed with: the first coordinate point at which the ratio of Si:C:O in the number of atoms is 1:1:0; the second coordinate point at which the ratio of SI:C:O in the number of atoms is 3:2:2; the third coordinate point at which the ratio of SI:C:O in the number of atoms is 1:2:2; and the fourth coordinate point at which the ratio of Si:C:O in the number of atoms is 1:2:0, but not on the line connecting the first coordinate point and the forth coordinate point.
- the liquid-repellent-layer base film 42A makes it possible, as shown in first and second examples to be described later, to obtain a high etching rate, greatly improve alkali resistance, and obtain a large contact angle, thereby improving liquid repellency.
- liquid-repellent-layer base film 42A has a film thickness of 50 nm or less. This makes it possible to perform laser ablation easily in forming the nozzles 2411, and prevent burrs from being left on the base part 41 and so forth.
- the base part 41 is made of silicon, metal material, or resin material.
- silicon as the base part 41 makes it possible to use photolithography or the like for nozzle processing. Such processing makes it possible to form the nozzles 2411 highly accurately and produce the inkjet heads 241 having few variations in ejection angles and high quality in image depiction.
- polyimide which is resin material
- the base part 41 makes it possible to improve heat resistance and perform annealing at a high temperature after forming the liquid-repellent-layer base film 42A or the liquid-repellent layer 43.
- PPS which is resin material, as the base part 41, can improve dimensional stability and reduce variations in nozzle length.
- SUS which is metal material, as the base part 41 makes it possible to easily form the nozzles 2411 by punch processing, laser processing, or electroforming on the SUS film.
- the inkjet recording device 1 includes the inkjet head 241 that has the nozzle substrate 40A, and the cleaning unit 27 that wipes off ink on the ejection surface side of the liquid-repellent layer 43. This can restrain effects of chemical mechanical polishing due to ink wiping by the cleaning unit 27, and realize the inkjet recording device 1 that prevents decrease in liquid repellency of the nozzle substrate 40A on the ejection surface side.
- the method for producing an inkjet head includes: a nozzle forming step of forming, in the base part 41, the nozzles 2411 that eject ink; a liquid-repellent-layer base film forming step of forming the liquid-repellent-layer base film 42A that has the silicon carboxide film on the ejection surface side of the base part 41; a liquid-repellent layer forming step of forming the liquid-repellent layer 43 on the ejection surface side of the liquid-repellent-layer base film 42A, thereby producing the nozzle substrate 40A; and an inkjet head producing step of producing the inkjet head 241 that includes the nozzle substrate 40A.
- the liquid-repellent-layer base film 42A made of the silicon carboxide film makes it possible to improve reactivity with the liquid-repellent agent for forming the liquid-repellent layer 43 and resistance to ink, particularly alkaline ink, of the nozzle substrate 40A on the ejection surface side, thereby preventing decrease of liquid repellency.
- the liquid-repellent-layer base film 42A of which outermost surface layer has a composition ratio in the range shown in FIG. 6A is formed by additional oxygenation on a silicon carbide film or a silicon carboxide film. Plasma treatment in an atmosphere containing oxygen gas is used as the oxygenation. This makes it possible to easily form the liquid-repellent-layer base film 42A as the silicon carboxide film having a composition ratio in the range shown in FIG. 6A .
- the number of siloxane bonding sites (-OH groups) on the surface of the silicon carboxide film can be increased, and fixability between the silicon carboxide film as the liquid-repellent-layer base film 42A and the liquid-repellent agent as the liquid-repellent layer 43 can be further improved.
- the liquid-repellent-layer base film 42A of which outermost surface layer has a composition ratio in the range shown in FIG. 6A is formed by additional carbon addition on a silicon oxide film or a silicon carboxide film. Plasma treatment in an atmosphere containing hydrocarbon gas is used as the carbon addition. This makes it possible to easily form the liquid-repellent-layer base film 42A as the silicon carboxide film having a composition ratio within the range shown in FIG. 6A .
- the nozzles 2411 are formed by excimer laser processing ablating the base part 41, the liquid-repellent-layer base film 42A, and the liquid-repellent layer 43. This makes it possible to perform laser ablation easily in the formation of the nozzles 2411, and prevent burrs from being left on the base part 41 and so forth.
- An inkjet recording device in this modification is configured as with the inkjet recording device I in the above embodiment, except that the nozzle substrate 40A is replaced with a nozzle substrate 40B.
- the same part as the above embodiment is not described, and the part different from the above embodiment is mainly described.
- FIG. 9 is a schematic cross-sectional view of the nozzle substrate 40B.
- the nozzle substrate 40B includes a base part 41, a liquid-repellent-layer base film 42B, and a liquid-repellent layer 43.
- the liquid-repellent-layer base film 42B is provided on the ejection surface side of the base part 41 and inside flow channels of the nozzles 2411. Part of the liquid-repellent-layer base film 42B constitutes a base layer of the liquid-repellent layer 43 on the base part 41 side.
- the liquid-repellent-layer base film 42B is a silicon carboxide film having a composition ratio in the preferable range shown in FIG. 6A .
- FIG. 10 is a flowchart showing a second nozzle substrate producing process.
- FIG. 11A is a schematic cross-sectional view of the base part 41 with the nozzles 2411 formed.
- FIG. 11B is a schematic cross-sectional view of the base part 41 with the liquid-repellent-layer base film 42B formed.
- FIG. 11C is a schematic cross-sectional view of the nozzle substrate 40B with the liquid-repellent layer 43 formed.
- the manufacturer performs nozzle processing on the flow channel side (back surface) of the base part 41, thereby forming the base part 41 as a base member with the nozzles 2411 formed (Step ST21).
- the base part 41 is made of, for example, metal material (SUS).
- the base part 41 with the nozzle 2411 formed can be formed by, for example, forming on a SUS film depressed portions having a depth larger than the thickness of the SUS film through punch processing, and smoothing and polishing bulged portions formed on the back surface of the SUS film.
- the base part 41 with the nozzles 2411 formed can be also formed by performing laser processing on the SUS film and forming the nozzles 2411.
- the base part 41 made of metal material with the nozzles 2411 formed can be also formed by electroforming.
- the manufacturer forms a silicon carboxide film having a composition ratio in the preferable range shown in FIG. 6A on the ejection surface side (front surface) and the flow channel side (back surface) of the base part 41 formed in Step ST21, thereby forming the liquid-repellent-layer base film 42B (Step ST22).
- the silicon carboxide film as the liquid-repellent-layer base film 42B in Step ST22, the surfaces of the liquid-repellent-layer base film and the flow channel protective film inside the flow channels can have high alkali resistance and chemical mechanical polishing resistance. Because siloxane bonds can be formed, the liquid-repellent-layer base film can have high fixability with the liquid-repellent agent.
- the silicon carboxide film can be formed, as with Step ST12 in FIG. 7 , using the methods (1) to (3) or the like.
- plasma treatment may be performed on the base part 41 as with Step ST 12 in FIG. 7 .
- reverse sputtering treatment may be performed on the base part 41.
- sputtering is performed on the base using oxygen gas, argon gas, or a mixture of these gases. Performing the reverse sputtering treatment can bring about effects of decontaminating or activating the surface of the base part 41 and improve adhesion between the liquid-repellent-layer base film 42B and the base part 41.
- the material gas may be hydrogenated.
- the hydrogenation may improve the stress, the film hardness, and the abrasion resistance of the liquid-repellent-layer base film 42B.
- the liquid-repellent-layer base film 42A may be formed by firstly forming a silicon oxide film or a silicon carboxide film and secondly introducing carbon to the film surface thereof, as with Step ST 12 in FIG. 7 .
- the liquid-repellent-layer base film 42B may be formed by: oxygenating a silicon carboxide film during film formation thereof; or, after forming a silicon carbide film or a silicon carboxide film, oxidizing the surface thereof as with Step ST 12 in FIG. 7 .
- the flow channel protective film can have high alkali resistance and high lyophilic property.
- the silicon carboxide film which has a high covalent bonding property and has hydroxy groups on the surface, is highly lyophilic (ink-philic, hydrophilic). This allows bubbles in the flow channels to easily escape when ink is introduced into the inkjet head 241, for example. Also, bubbles hardly adhere to the flow channels during operation of the inkjet head 241. Thus, ejection defects of the nozzles 2411 or the like are less likely to occur.
- the manufacturer forms the liquid-repellent layer 43 on the ejection surface side (front surface) of the base part 41, on which the liquid-repellent-layer base film 42B has been formed in Step ST22, thereby forming the nozzle substrate 40B (Step ST23), and ends the second nozzle substrate producing method.
- Step ST23 the liquid-repellent layer 43 is formed as with Step ST13 of FIG. 7 .
- Step ST23 it is possible to form the liquid-repellent layer 43 by: firstly forming a liquid-repellent layer on the ejection surface side (front surface), the inner walls of the nozzles 2411, and the flow channel side (back surface); and secondly removing all or part of the liquid-repellent layer on the inner walls of the nozzles 2411 and the flow channel side (back surface).
- removing method plasma treatment, chemical treatment, or the like can be used.
- a liquid-repellent layer may be formed on the ejection surface side (front surface), the inner walls of the nozzles 2411, and the flow channel side (back surface). Whereas the front surface of the nozzles 2411 contacts air, the inner walls of the nozzles 2411 and the inner walls of the flow channels are filled with ink, and no air is present. Therefore, the ink wettability of the inner walls of the nozzles 2411 and the inner walls of the flow channels may be lower than that of the front surface of the nozzles 2411.
- the nozzle substrate 40B of the inkjet head 241 has the liquid-repellent-layer base film 42B formed on the ejection surface side of the base part 41 and the inner walls of the nozzles 2411.
- the liquid-repellent-layer base film 42B which has high alkali resistance and high lyophilic property, can protect the ink flow channels.
- bubbles in the flow channels can easily escape when ink is introduced into the inkjet head 241, for example, and the bubbles hardly adhere to the flow channels during operation of the inkjet head 241.
- ejection defects of the nozzles 2411 or the like are less likely to occur.
- An inkjet recording device in this modification is configured as with the inkjet recording device 1 in the above embodiment, except that the nozzle substrate 40A is replaced with a nozzle substrate 40Ba.
- the same part as the above embodiment is not described, and the part different from the above embodiment is mainly described.
- FIG. 12 is a schematic cross-sectional view of the nozzle substrate 40Ba.
- the nozzle substrate 40Ba includes a base part 41, a liquid-repellent-layer base film 42A, a liquid-repellent layer 43, and a flow channel protective film 44B.
- the flow channel protective film 44B is provided on the ejection surface side of the base part 41 and inside the flow channels of the nozzles 2411.
- Part of the nozzle substrate 40Ba constitutes a base layer (film) of the liquid-repellent-layer base film 42A on the base part 41 side.
- the flow channel protective film 44B is a protective film having ink resistance.
- the method for producing the nozzle substrate 40Ba is the same as the producing method of the second nozzle substrate producing process in FIG. 10 .
- the manufacturer forms the flow channel protective film 44B on the ejection surface side and the flow channel side of the base part 41 with the nozzles 2411 formed in Step ST21.
- a metal oxide film containing one or more kinds of metal elements that are chemically stable in a high oxidation state such as tantalum, hafnium, niobium, titanium, and zirconium
- a metal oxide film has high alkali resistance.
- a metal silicate film may be used as the flow channel protective film 44.
- the metal silicate film is a silicon-containing metal oxide film containing one or more kinds of metal elements that are chemically stable in a high oxidation state, such as tantalum, hafnium, niobium, titanium, and zirconium.
- Examples of such a metal silicate film include tantalum silicate, hafnium silicate, niobium silicate, titanium silicate, and zirconium silicate.
- the metal silicate film has alkali resistance, and also has a lower ionic bonding property and a higher covalent bonding property by containing silicon. This increases the number of hydroxy groups of the flow channel protective film 44B and improves lyophilic property of the surface of the flow channel protective film 44B. With the improved lyophilic property, bubbles in the flow channels easily escape when ink is introduced into the inkjet head 241, for example, and bubbles hardly adhere to the flow channels during operation of the inkjet head 241. Thus, ejection defects of the nozzles 2411 or the like are less likely to occur.
- Step ST22 instead of the liquid-repellent-layer base film 42B, a liquid-repellent-layer base film 42A is formed on the ejection surface side of the base part 41 with the flow channel protective film 44B formed.
- the liquid-repellent-layer base film 42A is formed by: forming a liquid-repellent-layer base film on the ejection surface side and the flow channel side of the base part 41 with the flow channel protective film 44B formed; attaching a protective sheet on the ejection surface side of the base part 41 with the liquid-repellent-layer base film formed; removing the liquid-repellent-layer base film on the flow channel side through etching treatment or plasma treatment; and removing the protective sheet.
- Step ST23 is performed and the nozzle substrate 40Ba is produced.
- An inkjet recording device in this modification is configured as with the inkjet recording device 1 in the above embodiment, except that the nozzle substrate 40A is replaced with a nozzle substrate 40C.
- the same part as the above embodiment is not described, and the part different from the above embodiment is mainly described.
- FIG. 13 is a schematic cross-sectional view of the nozzle substrate 40C.
- the nozzle substrate 40C includes a base part 41, a liquid-repellent-layer base film 42A, a liquid-repellent layer 43, and a flow channel protective film 44.
- the flow channel protective film 44 is provided on the ejection surface side of the base part 41 and inside the flow channels of the nozzles 2411. Part of the flow channel protective film 44 constitutes a base layer (film) of the liquid-repellent-layer base film 42A on the base part 41 side.
- the flow channel protective film 44 is a protective film having ink resistance.
- FIG. 14 is a flowchart showing a third nozzle substrate producing process.
- FIG. 15A is a schematic cross-sectional view of the base part 41C.
- FIG. 15B is a schematic cross-sectional view of the base part 41C with the liquid-repellent-layer base film 42A formed.
- FIG. 15C is a schematic cross-sectional view of the base part 41C with nozzle holes 2411a formed.
- FIG. 15D is a schematic cross-sectional view of the base part 41C with ink channels 2411b formed.
- FIG. 15E is a schematic cross-sectional view of the base part 41C with the flow channel protective film 44 formed.
- FIG. 15F is a schematic cross-sectional view of the nozzle substrate 40C with the liquid-repellent layer 43 formed.
- the base part 41 is the base part 41C as an SOI (Silicon On insulator) substrate
- the nozzles 2411 are nozzles 2411C having nozzle holes and ink channels.
- the manufacturer prepares the base part 41C as an SOI substrate (Step ST31).
- the base part 41C has a supporting substrate 41a, a BOX (Buried Oxide) layer 41b, and an SOI layer 41c that are layered in this order.
- the base part 41C as the SOI substrate can be formed using a substrate bonding method, an SIMOX (Separation by IMplantation of OXygen) method, an ELTRAN (Epitaxial Layer TRANsfer), or the like.
- the film thickness of the SOI layer 41c should be between 10 and 100 ⁇ m inclusive, and the film thickness of the BOX layer 41b should be between 50 and 200 nm inclusive.
- a silicon oxide film or the like may be formed on the surface of the base part 41C, the surface being positioned on the SOI layer 41c side.
- the thickness of the supporting substrate 41a should be between 50 and 1,000 ⁇ m inclusive. Silicon may be used as the material of the supporting substrate 41a, although this is not a limitation. Quartz, glass, sapphire, SiC, GaN, YSZ, or the like may be used. Use of the base part 41C having the supporting substrate 41a made of an ink-resistant material makes it possible to produce the inkjet head 241 of which nozzles 2411C have highly ink-resistant inner walls and ink flow channels can be produced.
- the manufacturer forms a silicon carboxide film having a composition ratio in the preferable range shown in FIG. 6A on the ejection surface side (front surface) of the SOI layer 41c of the base part 41C, which has been prepared in Step ST31, thereby forming the liquid-repellent-layer base film 42A (Step ST32).
- the silicon carboxide film can be formed, as with Step ST 12 in FIG. 7 , using the methods (1) to (3) or the like.
- Step ST32 plasma treatment may be performed on the base part 41 as with Step ST 12 in FIG. 7 .
- Step ST32 reverse sputtering treatment may be performed on the base part 41.
- the material gas may be hydrogenated.
- the liquid-repellent-layer base film 42B may be formed by firstly forming a silicon oxide film or a silicon carboxide film and secondly introducing carbon to the film surface thereof, as with Step ST12 in FIG. 7 .
- the liquid-repellent-layer base film 42B may be formed by: oxygenating a silicon carboxide film during film formation thereof; or, after forming a silicon carbide film or a silicon carboxide film, oxidizing the surface thereof as with Step ST 12 in FIG. 7 .
- the above-described film formation methods and pretreatment methods may be appropriately combined, and are not limitations of the present invention.
- Step ST33 nozzle holes 2411a are formed by, for example, applying a resist to the surface of the liquid-repellent-layer base film 42A, forming a resist pattern by exposure, and performing dry etching. As the dry etching, Bosch process or the like can be used. It is preferable that the nozzle holes 2411a be reversely tapered as viewed from the SOI layer surface side.
- Such a reversely tapered shape becomes a normally tapered shape as viewed from the flow channel side when nozzles are finished, and stabilizes meniscus vibration when ink droplets are ejected. This realizes the inkjet head 241 having excellent ejection characteristics.
- the manufacturer performs ink channel processing on the flow channel side (back surface) of the supporting substrate 41a and the BOX layer 41b of the base part 41C, in which the nozzle holes 2411a have been formed in Step ST33 (Step ST34).
- the ink channels 2411b are formed by, for example, applying a resist to the back surface of the supporting substrate 41a, forming a resist pattern by exposure, and performing dry etching.
- the supporting substrate 41 a may be polished to make it thin so as to have the supporting substrate 41a of a desired size.
- the manufacturer forms a flow channel protective film 44 on the flow channel side (back surface) of the base part 41C with the ink channels 2411b (nozzles 2411C) formed in Step ST34 (Step ST35).
- a metal oxide film containing one or more kinds of metal elements that are chemically stable in a high oxidation state such as tantalum, hafnium, niobium, titanium, and zirconium, may be used. Such a metal oxide film has high alkali resistance.
- a metal silicate film may be used as the flow channel protective film 44.
- the metal silicate film is a silicon-containing metal oxide film containing one or more kinds of metal elements that are chemically stable in a high oxidation state, such as tantalum, hafnium, niobium, titanium, and zirconium.
- metal elements that are chemically stable in a high oxidation state
- examples of such a metal silicate film include tantalum silicate, hafnium silicate, niobium silicate, titanium silicate, and zirconium silicate. Containing silicon, the metal silicate film, which has alkali resistance, has a low ionic bonding property and a high covalent bonding property. This increases the number of hydroxy groups of the flow channel protective film 44B and improves lyophilic property of the surface of the flow channel protective film 44B.
- a silicon carboxide film may be used as the flow channel protective film 44.
- Use of the silicon carboxide film as the flow channel protective film 44 can produce the flow channel protective film having high alkali resistance and high lyophilic property.
- the silicon carboxide film which has a high covalent bonding property and has hydroxy groups on the surface, is highly lyophilic. This allows bubbles in the flow channels to easily escape when ink is introduced into the inkjet head 241, for example. Also, bubbles hardly adhere to the flow channels during operation of the inkjet head 241. Thus, ejection defects of the nozzles or the like are less likely to occur.
- a silicon carboxide film may be additionally layered on the whole of or part of the upper layer of the flow channel protective film 44 made of the metal oxide or the metal silicate film. The nozzle substrate 40C may not have the flow channel protective film 44.
- the manufacturer forms a liquid-repellent layer on the ejection surface side (front surface) of the base part 41C, on which the flow channel protective film 44 has been formed in Step ST35, and the liquid-repellent-layer base film 42A, thereby forming the nozzle substrate 40C (Step ST36), and ends the third nozzle substrate producing method.
- Step ST36 the liquid-repellent layer 43 is formed as with Step ST13 of FIG. 7 .
- Step ST36 it is possible to form the liquid-repellent layer 43 by: firstly forming a liquid-repellent layer on the ejection surface side (front surface), the inner walls of the nozzles 2411C, and the flow channel side (back surface); and secondly removing all or part of the liquid-repellent layer on the inner walls of the nozzles 2411C and the flow channel side (back surface).
- removing method plasma treatment, chemical treatment, or the like can be used.
- a liquid-repellent layer may be formed on the ejection surface side (front surface), the inner walls of the nozzles 2411C, and the flow channel side (back surface).
- the front surface of the nozzles 2411 C contacts air
- the inner walls of the nozzles 2411C and the inner walls of the flow channels are filled with ink, and no air is present. Therefore, the ink wettability of the inner walls of the nozzles 2411C and the inner walls of the flow channels may be lower than that of the front surface of the nozzles 2411C.
- the nozzle substrate 40C of the inkjet head 241 includes the flow channel protective film 44 formed inside the flow channels of the nozzles 2411.
- the flow channel protective film 44 can protect the ink flow channels. Further, use of the silicon carboxide film as the flow channel protective film 44 allows bubbles in the flow channel to easily escape when ink is introduced into the inkjet head 241, for example. Also, bubbles hardly adhere to the flow channels during operation of the inkjet head 241. Thus, ejection defects of the nozzles 2411 or the like are less likely to occur.
- FIG. 16 is a diagram showing coordinate points PSA and PSB of samples SA and SB, respectively, in the triangular diagram showing the ratio of Si:C:O in the number of atoms.
- the sample SA as an example of the silicon carboxide film Si a C b O c was produced.
- O 2 plasma treatment was performed on a base (Si wafer) by RIE-10NR manufactured by Samco.
- a silicon carboxide film was formed on the base (Si wafer) using TEOS (TEtraethOxySilane) by a film forming apparatus (Plasma CVD apparatus PD-200ST manufactured by Samco).
- the sample SB being a silicon oxide film was also produced.
- film formation pretreatment was performed on the base (Si wafer) of the sample SB.
- a silicon carboxide film as the sample SB was formed on the base (Si wafer) using TEOS by the film forming apparatus (Plasma CVD apparatus PD-200ST manufactured by Samco).
- the composition ratio of Si, C, and O of each of the samples SA and SB was evaluated by an X-ray photoelectron spectrometer (QuanteraSXM manufactured by ULVAC-PHI).
- the coordinate points PSA and PSB corresponding to the samples SA and SB, respectively, are plotted in the triangular diagram showing the ratio of Si, C, and O in the number of atoms.
- the coordinate point PSA of the sample SA is included in the preferable range of the composition ratio of Si:C:O shown in FIG. 6A .
- the sample SB is a silicon oxide film, and the coordinate point PSB is not included in the same preferable range of composition ratio
- the etching rate of the silicon carboxide film as the sample SA was about 1/300 of the etching rate of the silicon oxide film as the sample SB. This shows that the use of a silicon carboxide film like the sample SA as the liquid-repellent-layer base films 42A, 42B greatly improves alkali resistance of the liquid-repellent-layer base films 42A, 42B.
- FIG. 17 is a diagram showing coordinate points and contact angles of samples S1 to S9, respectively, in the triangular diagram showing the ratio of Si:C:O in the number of atoms.
- the sample S1 is silicon
- the samples S2 and S3 are silicon oxide films
- the sample S4 is a silicon carbide film.
- coordinate points PS1, PS2, PS3, PS4, PS5, PS6, PS7, PS7, PS8, and PS9 corresponding to the samples S1, S2, S3, S4, S5, S6, S7, S8, and S9, respectively, are plotted in the triangular diagram showing the ratio of SI:C:O in the number of atoms.
- a liquid-repellent layer was formed as the liquid-repellent layer 43 by application.
- Conditions of the application were as follows: the samples S1 to S9 were dipped in 0.1% OPTOOL solution for three minutes, and pulled up at a low speed (10 mm/sec); and ultrasonic cleaning (ultrasonic frequency 950 kHz for 20 minutes) was performed.
- each of the samples S1 to S9 with the liquid-repellent layer formed was immersed in an aqueous alkaline dummy ink having a pH of 11.
- Contact angles (static contact angle, receding contact angle) of the dummy ink were then measured to evaluate change in contact angles.
- the aqueous alkaline dummy ink having a pH of 11 was an aqueous solution in which a buffer solution of sodium carbonate, potassium carbonate, or the like was mixed with polypropylene glycol alkyl ether, dipolypropylene glycol alkyl ether, tripolypropylene glycol alkyl ether, or the like to adjust its pH to between 10 and 11 inclusive.
- the dummy ink to measure the contact angles was: diethylene glycol alkyl ether; triethylene glycol alkyl ether; tetraethylene glycol alkyl ether; polypropylene glycol alkyl ether; dipolypropylene glycol alkyl ether; tripolypropylene glycol alkyl ether; or a mixture of a plurality of solvents selected from these.
- the static contact angle and the receding contact angle of the dummy ink on each of the samples S1 to S9 with the liquid-repellent layer formed were as shown in the table III.
- the contact angles of each of the samples S1 to S9 are expressed by the size (diameter) of a circle centered at each of the coordinate points PS1 to PS9.
- the samples S5, S7, and S9 each having a composition ratio in the preferable range shown in FIG. 6A obtained preferable contact angles even in a deteriorated state after being immersed in the alkaline ink, and obtained preferable liquid repellency.
- the increase in the number of hydroxy groups on the surface of the liquid-repellent-layer base film increased density of Si-O bonds formed between the compound forming the liquid-repellent layer and the liquid-repellent-layer base film, and consequently restrained the liquid-repellent material from desorbing from the liquid-repellent-layer base film, which is caused by alkaline hydrolysis.
- the nozzle substrate described in the above embodiments and modifications is the nozzle substrate for a bend-mode inkjet head in which a plurality of substrates are layered, the present invention is not limited to this.
- the nozzle substrate in the above embodiment and the modifications may be applied to a nozzle substrate of a shear-mode inkjet head that presses ink in channels by applying an electric field in a direction perpendicular to the poling direction of a piezoelectric element and shearing the piezoelectric element.
- an inkjet head, an inkjet recording device, and a method for producing an inkjet head in the present invention can be applied to image recording using ink.
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Description
- The present invention relates to an inkjet head, an inkjet recording device, and a method for producing an inkjet head.
- There has been known an inkjet recording device (inkjet printer) that ejects (discharges) ink droplets from nozzles of inkjet heads, thereby forming an image on a recording medium. When the inkjet recording device ejects ink droplets, ink may adhere to nozzle surfaces (around the openings of the nozzles on the ejection side) of the inkjet heads owing to the influence of ink mist generated in the printer or ink bounced by the recording medium. It is known that ink adhering to the nozzle surfaces affects ejection angles of ink droplets when the ink droplets are ejected from the nozzles and changes the ejection angles.
- In order to prevent adhesion of ink to nozzle surfaces, there is known a method of forming an ink-repellent layer on nozzle surfaces by coating the nozzle surfaces with an ink-repellent agent. As the ink-repellent layer, there is known a film formed by bonding organic functional groups containing fluorine through dehydration-condensation reactions with silane coupling ([-OH] + [HO-Si-R-F] → [H2O] + [-O-Si-R-F]) (see Patent Literature 1). Silanol groups in the compound of the silane coupling agent and hydroxy groups on the surface of a base film form siloxane bonds. It is desirable that the base film have a strong covalent bonding property. It is known that a base film having a strong ionic bonding property does not form siloxane bonds (see Non-Patent literature 1).
- Further, there is proposed a nozzle substrate that has inner walls of nozzle holes and a plurality of layers of ink resistant protective films (see Patent Literature 2). First, a thermal oxide film having a high coating property is formed. Next, a metal oxide having ink resistance is formed on the inner walls, the front surface, and the back surface by a CVD (Chemical Vapor Deposition) method, and then a water-repellent film is formed on the ejection surface side. As the ink-resistant protective film, a metal oxide, such as tantalum pentoxide, hafnium oxide, niobium oxide, titanium oxide, or zirconium oxide, is used. This is because these metal oxides are highly resistant to alkaline ink (discharging liquid). Also, the water-repellent film preferably contains a fluorine-containing organosilicon compound as a main component. This is because hydroxy groups on the surface of the ink-resistant protective film firmly bond with hydrolyzing groups, such as methoxy groups, of the fluorine-containing organosilicon compound, so that adhesion between the ink-resistant protective film and the water-repellent film formed on the surface of the ink-resistant protective film is improved.
- Patent Literature 3 discloses an inkjet head according to the preamble of
claim 1 and a method for producing an inkjet head according to the preamble of claim 7. - Also, there is known a wiping method of wiping off ink on a liquid-repellent layer (water-repellent film) of a nozzle substrate of an inkjet head of an inkjet recording device.
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- Patent Literature 1:
JP 2007-230061 A - Patent Literature 2:
JP 5145985 B - Patent Literature 3:
JP 2013-188874 A -
- Non-Patent literature 1: Yoshinobu NAKAMURA, Kazuya NAGATA, et al. "Effects and usage of silane coupling agents (Silane-coupling-zai no kouka to shiyouhou)", S&T Publishing, November 15, 2012.
- Non-Patent literature 2: Takeshi OWAKI, Yasunori TAGA, "Journal of the Surface Finishing Society of Japan", vol. 49, p. 191-194, 1998
- In
Patent Literature 2, metal elements that may be contained in a metal oxide film used as a protective film, such as tantalum pentoxide, hafnium oxide, niobium oxide, titanium oxide, and zirconium oxide, are transition metal elements in the group 4 or the group 5. It is known that these metal elements in their oxidation states are highly stable and their outermost shell orbitals are filled with electrons and their internal orbitals are unfilled. That is, the bonding of these metal oxide films has a strong ionic bonding property compared with the bonding of oxide films made of typical elements, such as SiO2, as shown in the table I. This leads to low reactivity to the silane coupling agent (liquid-repellent agent, water-repellent agent).[Table I] OXIDE IONIC BONDING PROPERTY NON-PATENT LITERATURE 1NON-PATENT LITERATURE 2TiO2 0.6 0.65 Ta2O5 - 0.6 SiO2 0.5 0,5 SiC 0.1 - In addition, in the structure in which the liquid-repellent layer is formed on the metal oxide film, a liquid repellency (water repellency, ink repellency) is decreased by wiping.
- Objects of the present invention include improving reactivity with the liquid-repellent agent and resistance to ink of the nozzle substrate on the ejection surface side, thereby preventing decrease in liquid repellency of the nozzle substrate on the ejection surface side.
- In order to solve the above problem(s), the present invention is defined in the appended claims.
- The present invention can improve reactivity with the liquid-repellent agent and resistance to ink of the nozzle substrate on the ejection surface side, and prevent decrease in liquid repellency of the nozzle substrate on the ejection surface side.
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FIG. I is a schematic view of configuration of an inkjet recording device according to an embodiment of the present invention viewed from the front side. -
FIG. 2A is a schematic configuration diagram of a head unit located above the conveying surface of an image forming drum viewed from the upstream side in the conveying direction of recording media. -
FIG. 2B is a bottom view of the head unit viewed from the conveying surface side of the image forming drum. -
FIG. 3A is a perspective view of the image forming drum. -
FIG. 3B is an illustration behind the image forming drum viewed from the same front side asFIG. 1 , wherein the image forming drum is seen through. -
FIG. 4 is a schematic view of a cross-sectional shape of an inkjet head. -
FIG. 5 is a schematic cross-sectional view of a first nozzle substrate of the embodiment. -
FIG. 6A shows a preferable range of a composition ratio of a silicon carboxide film in a triangular diagram showing a ratio of SI:C:O in the number of atoms. -
FIG. 6B shows a coordinate point in the triangular diagram showing the ratio of Si:C:O in the number of atoms. -
FIG. 7 is a flowchart showing a first nozzle substrate producing process. -
FIG. 8A is a schematic cross-sectional view of a base part before nozzle processing. -
FIG. 8B is a schematic cross-sectional view of the base part with a liquid-repellent-layer base film formed. -
FIG. 8C is a schematic cross-sectional view of the base part with a liquid-repellent layer formed. -
FIG. 8D is a schematic cross-sectional view of the base part with a protective sheet attached. -
FIG. 8E is a schematic cross-sectional view of the base part with nozzles formed. -
FIG. 8F is a schematic cross-sectional view of a first nozzle substrate with the protective sheet removed. -
FIG. 9 is a schematic cross-sectional view of a second nozzle substrate. -
FIG. 10 is a flowchart showing a second nozzle substrate producing process. -
FIG. 11A is a schematic cross-sectional view of a base part with nozzles formed. -
FIG. 11B is a schematic cross-sectional view of the base part with a liquid-repellent-layer base film formed. -
FIG. 11C is a schematic cross-sectional view of a second nozzle substrate with a liquid-repellent layer formed. -
FIG. 12 is a schematic cross-sectional view of a third nozzle substrate. -
FIG. 13 is a schematic cross-sectional view of a fourth nozzle substrate. -
FIG. 14 is a flowchart showing a third nozzle substrate producing process. -
FIG. 15A is a schematic cross-sectional view of a base part. -
FIG. 15B is a schematic cross-sectional view of the base part with a liquid-repellent-layer base film formed. -
FIG. 15C is a schematic cross-sectional view of the base part with nozzle holes formed. -
FIG. 15D is a schematic cross-sectional view of the base part with ink channels formed. -
FIG. 15E is a schematic cross-sectional view of the base part with a flow channel protective film formed. -
FIG. 15F is a schematic cross-sectional view of a fourth nozzle substrate with a liquid-repellent layer formed. -
FIG. 16 shows coordinate points of first and second samples in the triangular diagram showing the ratio of Si:C:O in the number of atoms. -
FIG. 17 shows coordinate points and contact angles of third to 11th samples in the triangular diagram showing the ratio of Si:C:O in the number of atoms. - With reference to the attached figures, an embodiment, first, second and third modifications, and first and second examples according to the present invention are described in detail in order. It should be noted that the present invention is not limited to illustrated examples. In the following description, components having the same function and configuration are denoted by the same reference numeral and descriptions thereof are omitted.
- With reference to
FIGS. 1 to 8F , an embodiment according to the present invention is described. First, configuration of aninkjet recording device 1 of this embodiment is described with reference toFIGS. 1 to 3B .FIG. 1 is a schematic view of configuration of theinkjet recording device 1 of this embodiment viewed from the front. - The
inkjet recording device 1 includes amedium supplying unit 10, animage forming unit 20, amedium receiving unit 30, and a controller (not illustrated). In theinkjet recording device 1, recording media R stored in themedium supplying unit 10 are conveyed to theimage forming unit 20 in accordance with control operation performed by the controller, and, after images are formed, discharged to themedium receiving unit 30. - The
medium supplying unit 10 includes amedium supplying tray 11 and a conveyingunit 12. Themedium supplying tray 11 is a plate-shaped member provided so as to be able to store one or more recording media R. Themedium supplying tray 11 moves up and down according to the amount of recording media R, and the top recording medium R among the recording media R stored thereon is placed at the conveyance start position of the conveyingunit 12. As recording media R, various types of recording media that can be held to be curved on the outer circumferential surface of animage forming drum 21, such as printing paper, cellophane, films and fabrics having various thicknesses, are used. - The conveying
unit 12 includes a plurality of (for example, two)rollers belt 123 supported by therollers medium supplying tray 11 to thebelt 123. According to the circling movement of thebelt 123 driven by the rotation of therollers unit 12 conveys and sends the recording medium R, which has been delivered onto thebelt 123 by the supplying unit, to theimage forming unit 20. - The
image forming unit 20 includes theimage forming drum 21, a first deliveringunit 22, atemperature measuring unit 23,head units 24, aheating unit 25, a second deliveringunit 26, and cleaning units 27 (seeFIGS. 3A and 3B ). - The
image forming drum 21 has a cylindrical outer circumferential surface. Theimage forming drum 21 holds the recording medium R on the outer circumferential surface (conveying surface) and conveys the recording medium R along a conveying path according to rotating operation of theimage forming drum 21. On the inner surface side of theimage forming drum 21, a heater is provided. The heater can heat the conveying surface so that the recording medium R placed on the conveying surface has a predetermined temperature. - The first delivering
unit 22 delivers the recording medium R delivered by the conveyingunit 12 to theimage forming drum 21. The first deliveringunit 22 is provided at a position between the conveyingunit 12 of themedium supplying unit 10 and theimage forming drum 21. The first deliveringunit 22 includes a claw part(s) 221 that grips one end of the recording medium R conveyed by the conveyingunit 12 and a cylindrical deliveringdrum 222 that leads the recording medium R gripped by theclaw part 221. The recording medium R that theclaw part 221 has received from the conveyingunit 12 is sent to the deliveringdrum 222, moves along the outer circumferential surface of the rotating deliveringdrum 222, and is led to and delivered to the outer circumferential surface of theimage forming drum 21. - The
temperature measuring unit 23 is provided at a position between the point where the recording medium R is placed on the conveying surface of theimage forming drum 21 and the point where the recording medium R faces an ink ejection surface (jetting surface) of ahead unit 24 that the recording medium R faces first. Thetemperature measuring unit 23 measures temperature of a surface of the recording medium R (temperature of the surface opposite to the surface contacting the conveying surface) being conveyed. As a temperature sensor of thetemperature measuring unit 23, a radiation thermometer is used, for example. The radiation thermometer measures the surface temperature of the recording medium R, which does not contact the temperature measuring unit 23 (radiation thermometer), by measuring intensity distribution of infrared rays. Thetemperature measuring unit 23 has a plurality of sensors arranged along a width direction perpendicular to the direction in which the recording medium R is conveyed in the image forming unit 20 (conveying direction), the width direction being perpendicular to the surface ofFIG. 1 , so as to be able to measure temperature at a plurality of points. Each measurement data is output to the controller at an appropriate predetermined timing to be controlled. - In accordance with the rotation of the
image forming drum 21 holding the recording medium R, each of thehead units 24 ejects (discharges) ink droplets at positions on the recording medium R from a plurality of nozzle opening parts (nozzle holes) formed on the ink ejection surface that faces the recording medium R, thereby forming an image. Theinkjet recording device 1 in this embodiment has fourhead units 24 that are arranged a predetermined distance away from the outer circumferential surface of theimage forming drum 21 and at predetermined intervals from one another. The fourhead units 24 output ink of four colors: C (Cyan), M (Magenta), Y (Yellow), and K (Black), respectively. Herein, the C, M, Y, and K inks are ejected in this order from the upstream side in the conveying direction of the recording medium R. Although any ink can be used, a normal liquid ink is herein used. The ink fixes to the recording medium R when ink evaporates and dries by the operation of theheating unit 25. Each of thehead units 24 has a line scan head that is capable of forming an image over an image forming width on the recording medium R in combination with the rotation of theimage forming drum 21. - The
heating unit 25 heats the surface of the recording medium R being conveyed. For example, theheating unit 25 heats the recording medium R by generating heat with an electric heating wire being energized and heating the air, or by emitting infrared rays. Theheating unit 25 is provided at a position close to the outer circumferential surface of theimage forming drum 21 so as to be able to heat the recording medium R until theimage forming drum 21 delivers the recording medium R to the second deliveringunit 26 after thehead units 24 eject ink onto the recording medium R conveyed by the rotation of theimage forming drum 21. The operation of theheating unit 25 dries the ink ejected from the nozzles of thehead units 24 and fixes the ink to the recording medium R. - The second delivering
unit 26 conveys the recording medium R on which the ink has been ejected and fixed from theimage forming drum 21 to themedium receiving unit 30. The second deliveringunit 26 includes a plurality of (for example, two)rollers belt 263 supported by therollers cylindrical delivery roller 264. The second deliveringunit 26 leads the recording medium R on theimage forming drum 21 onto thebelt 263 with thedelivery roller 264, moves the recording medium R, which is received, together with thebelt 263 that circulates in accordance with the rotation of therollers medium receiving unit 30. - The cleaning
units 27 perform cleaning operation of the ink ejection surfaces of thehead units 24. The cleaningunits 27 are each provided adjacent to theimage forming drum 21 in the width direction. When thehead units 24 move in the width direction, the ink ejection surfaces of thehead units 24 are set at the cleaning positions where thecleaning units 27 perform cleaning. - The
medium receiving unit 30 stores the recording medium R sent from theimage forming unit 20 after image formation until a user takes out the recording medium R. Themedium receiving unit 30 includes a plate-shapedmedium receiving tray 31 on which the recording medium R conveyed by the second deliveringunit 26 is stored. -
FIGS. 2A and 2B are illustrations showing configuration of thehead unit 24.FIG. 2A is a schematic structural view of thehead unit 24 located above the conveying surface of theimage forming drum 21 viewed from the upstream side in the conveying direction of the recording medium R.FIG. 2B is a bottom view of thehead unit 24 viewed from the conveying surface side of theimage forming drum 21. - The
head unit 24 has a plurality of inkjet heads 241. Herein, onehead unit 24 has 16 inkjet heads 241, although the present invention is not limited to this. The 16 inkjet heads 241 make eight sets ofinkjet modules 242, wherein a pair of inkjet heads 241 are included in oneinkjet module 242. Herein, theinkjet modules 242 are fixed to a fixingmember 245 so as to be staggered in appropriate relative positions. - The fixing
member 245 is supported and held by acarriage 246. Thecarriage 246 also holds afirst sub-tank 243 andsecond sub-tanks 244 to feed ink to the inkjet heads 241. Thecarriages 246 of the respective fourhead units 24 are individually movable in the width direction over theimage forming drum 21. - As shown in
FIG. 2B , each of the inkjet heads 241 has a plurality ofnozzles 2411. Theinkjet head 241 ejects ink (droplets) from opening parts (nozzle holes) ofnozzles 2411 formed on the bottom surface of the inkjet head 241 (nozzle opening surface 241a), so that the ink droplets land on the recording medium R held on the conveying surface of theimage forming drum 21. Although each of the inkjet heads 241 shown here has the opening parts of thenozzles 2411 arranged in two rows in the conveying direction in a two-dimensional array pattern, the present invention is not limited to this. The opening parts of thenozzles 2411 may be arranged in an appropriate one-dimensional or two-dimensional array pattern. The arrangement range of these opening parts of all the 16 inkjet heads 241 covers, in the width direction, the recordable width of the recording medium R held on the conveying surface. This enables one-pass image forming with thehead units 24 fixed. The nozzle opening surfaces 241a of the 16 inkjet heads 241 are covered with a liquid-repellent layer 43 (water-repellent layer, ink-repellent layer) (seeFIG. 5 ). -
FIGS. 3A and 3B are illustrations to explain configuration of thecleaning unit 27.FIG. 3A is a perspective view of theimage forming drum 21.FIG. 3B is a view behind theimage forming drum 21 viewed from the same front side asFIG. 1 , wherein theimage forming drum 21 is seen through. - The
cleaning unit 27 wipes off ink and other impurities (collectively called foreign elements) adhering to the nozzle opening surfaces 241a of the inkjet heads 241, thereby removing them after ink is ejected for image formation and/or maintenance is performed. As shown inFIG. 3A , thecleaning unit 27 is arranged next to theimage forming drum 21 in the width direction so that the ink ejection surface can be cleaned when thehead unit 24 moves in the width direction. - As shown in
FIG. 3B , thecleaning unit 27 includes a wipingmember 271, anelastic member 272, an unwindingroller 273, and a windingroller 274. Although this configuration is provided to each of thehead units 24, the configuration may be shared by thehead units 24 by making thecleaning unit 27 movable in the conveying direction. - The wiping
member 271 is a long cloth-like sheet member of which length (width) in the width direction can cover the ink ejection surface (at least all the nozzle opening surfaces 241a). A desirable member as the wipingmember 271 is the one that easily absorbs moisture of ink, has lower hardness than the hardness of the material of the ink ejection surface, and hardly damages the liquid-repellent layer. Examples of such a member include polyester, acrylic, polyamide, and polyurethane that can form a woven or non-woven fabric. In particular, a member that has a high water-absorbing property and can easily absorb liquid with a low pressing force at the time of contact is further preferable. Alternatively, the wipingmember 271 may have a blade-like structure. - The
elastic member 272 faces the ink ejection surface with the wipingmember 271 in between. The surface (pressing surface) of theelastic member 272 facing the ink ejection surface has a size that can cover the entire ink ejection surface. Theelastic member 272 is movable approximately perpendicular to the ink ejection surface. As a material of theelastic member 272, materials that do not damage nozzles when pressed against thenozzle opening surfaces 241a, such as a sponge (foamed resin) and rubber, are used. The wipingmember 271 contacts the nozzle opening surfaces 241a (ink ejection surface) in a state of being approximately parallel to thenozzle opening surfaces 241a as a whole by being moved in a direction to approach the nozzle opening surfaces 241a. - Herein, the relative positions (distance) of the
elastic member 272 and the ink ejection surface when the wipingmember 271 contacts thenozzle opening surfaces 241a are fixed. This makes the pressing force of the wipingmember 271 against the ink ejection surface the same every time within a range of effects of the liquid-repellent layer that peels off from the surface of the nozzle opening surfaces 241a. The relative positions of theelastic member 272 and the ink ejection surface are determined so as to have an appropriate level of the pressing force for cleaning the ink on the ink ejection surface. Alternatively, the pressing force may be variable. In such a case, the maximum value of the pressing force is determined according to a relationship between the surface shape of the nozzle opening surfaces 241a and the wipingmember 271, as described later. - The wiping
member 271 is unwound from the unwindingroller 273 and wound up by the windingroller 274 in accordance with winding operation performed by the windingroller 274. During this time, theelastic member 272 presses the wipingmember 271 against the ink ejection surface approximately uniformly. This makes the clean (with no ink adhered) wipingmember 271 contact the ink ejection surface and clean ink or the like adhering to the nozzle opening surfaces 241a (ink ejection surface). If thewhole wiping member 271 is unwound from the unwindingroller 273, the wipingmember 271 can be replaced easily. - Next, a
nozzle substrate 40A provided on the ink ejection surface of thehead unit 24 of this embodiment is described in detail.FIG. 4 is a schematic view of a cross-sectional shape of theinkjet head 241. - The inkjet heads 241, although not particularly limited, is a bend-mode inkjet head that is formed with a plurality of plates (substrates) layered as shown in
FIG. 4 . More specifically, each of the inkjet heads 241 includes thenozzle substrate 40A, a pressure chamber substrate 50, anoscillating plate 60, aspacer substrate 70, and awiring substrate 80 layered in this order from the side where thenozzle opening surface 241a (ink ejection surface, lower side) are provided to the upper side. - Ink supplied from the
first sub-tank 243 and thesecond sub-tanks 244 flows into thepressure chamber 51 of the pressure chamber substrate 50 through an ink flow channel(s) that communicates with thewiring substrate 80, thespacer substrate 70, and theoscillating plate 60. Thepressure chamber 51 abuts thepiezoelectric element part 71 of thespacer substrate 70 with theoscillating plate 60 in between, and electrically connects to thenozzle 2411. When a control signal from the controller of theinkjet recording device 1 is input to thepiezoelectric element part 71 through a wire(s) of thewiring substrate 80, thepiezoelectric element part 71 physically oscillates. This causes ink in the ink flow channel in thewiring substrate 80 and so forth to flow into thepressure chamber 51, and causes the ink in thepressure chamber 51 to flow into thenozzle 2411 of the nozzle substrate 40. Then, the ink in thenozzle 2411 is ejected as ink droplets from the opening part (nozzle hole) on the side where thenozzle opening surface 241a (ejection surface) is provided, and the ink droplets land on the recording medium R. - There may be provided, between the
nozzle substrate 40A and the pressure chamber substrate 50, an intermediate substrate (intermediate layer) having a flow channel that connects thepressure chamber 51 and thenozzle 2411. - Next, configuration of the
nozzle substrate 40A is described with reference toFIG. 5. FIG. 5 is a schematic cross-sectional view of thenozzle substrate 40A. InFIG. 5 showing thenozzle substrate 40A, the lower part of the drawing is referred to as the (ink) ejection surface side (extemal side of the head), and the upper part of the drawing is referred to as the flow channel side (internal side of the head, pressure chamber side). The same applies to cross-sectional views of the other nozzle substrates and cross-sectional views thereof in producing steps. - As shown in
FIG. 5 , thenozzle substrate 40A includes abase part 41, a liquid-repellent-layer base film 42A, and a liquid-repellent layer 43. Examples of a material of thebase part 41 include silicon; metal, such as SUS (Steel Use Stainless), nickel, and metal containing nickel; and resin, such as polyimide. - If silicon is used as the base, processes, such as photolithography used in semiconductor processing, can be performed for nozzle processing. Using such a process enables highly precise nozzle processing and production of inkjet heads having few variations in ejection angles and high quality in image depiction.
- The
nozzle 2411 is an ink nozzle formed in thebase part 41, and includes an ink flow channel and a nozzle hole on the ejection surface side. The liquid-repellent-layer base film 42A is provided on the ejection surface side, where thecleaning unit 27 wipes off ink during maintenance of thebase part 41, and is the base layer of the liquid-repellent layer 43 on the flow channel side (base part 41 side). In this embodiment, the material of the liquid-repellent-layer base film 42A is silicon carboxide (silicon carboxide film) SiaCbOc (a, b, c: the number of atoms). The liquid-repellent layer 43 is provided on the ejection surface side of the liquid-repellent-layer base film 42A, and has, for example, a structure having perfluorocarbon chains and has ink-repellent properties (water repellency, ink repellency). - The reason that the silicon carboxide film is selected as the liquid-repellent-
layer base film 42A in this embodiment is that the silicon carboxide film can achieve alkali resistance, chemical mechanical polishing (CMP) resistance, and fixability of the liquid-repellent agent (siloxane bonds can be formed). More specifically, the chemical mechanical polishing resistance is resistance to film reduction of the liquid-repellent-layer base film due to ink wiping by thecleaning unit 27. In particular, as a maintenance of an inkjet recording device using alkaline ink, ink on an ejection surface of a nozzle substrate is wiped off with a cloth or the like of a cleaning unit. This makes a liquid-repellent layer of a conventional liquid-repellent-layer base film of the nozzle substrate to peel off easily. This may result in decrease in ink resistance of the nozzle substrate. Silicon carbide SiC ranks second to DLC (diamond-like carbon) in hardness and is known as a material that is hardly alkali-etched. Use of a silicon carboxide film that is produced by introducing carbon into silicon oxide as the liquid-repellent-layer base film 42A makes it possible to improve its alkali resistance as well as to maintain reactivity thereof with the silane coupling agent on the nozzle surface. - Inkjet printing has been aggressively used in the textile field recently. In comparison with the conventional textile printing methods, the inkjet printing has merits of: requiring no plates to be generated; being applicable to small lot production; and having less ink waste. In a case of using polyester or synthetic fiber as recording media R, an aqueous ink, such as a disperse dye ink or a sublimation dye ink, is used. However, an additive to the ink, such as a dispersant, is alkaline. With respect to ink containing pigment molecules, dispersion of the pigment molecules is controlled with pH of the ink. The conventional liquid-repellent layer formed by silane coupling has low reliability because, in an alkaline environment, hydrolysis of the liquid-repellent layer is accelerated or desorption of the liquid-repellent material is accelerated by the etching of the liquid-repellent-layer base film. Even if textile-printing ink itself is neutral or slightly alkaline, a fabric coated with an alkaline pretreatment agent may be used to improve color development. In an inkjet printer for textile printing, the alkaline pretreatment agent on the fabric surface may affect reliability of liquid repellency of the surface of the subsequent inkjet head owing to raising treatment or the like.
- On the other hand, the silicon carboxide film has high chemical stability and can improve alkali resistance. With reference to
FIGS. 6A and 6B , the composition ratio of the silicon carboxide film SiaCbOc having high alkali resistance is described.FIG. 6A is a diagram showing a preferable range of the composition ratio of the silicon carboxide film in a triangular diagram showing the ratio of Si, C, and O in the number of atoms.FIG. 6B is a diagram showing a coordinate point P0 in the triangular diagram showing the ratio of Si:C:O in the number of atoms. - As shown in
FIG. 6A , the composition ratio (ratio in the number of atoms) of silicon Si, carbon C, and oxygen O of the silicon carboxide film is shown in the triangular diagram that is an equilateral triangle having three vertexes corresponding to Si only, C only, and O only, respectively. As shown inFIG. 6B , in the triangular diagram showing composition of Si, C, and O, the vertexes corresponding to only Si, C, and O are referred to as VSi, VC, and VO, respectively. At an arbitrary coordinate point P0 in the triangular diagram, the coordinates thereof are represented by a length α on the side from vertex VO to vertex VSi, a length β on the side from vertex VSi to vertex VC, and a length γ on the side from vertex VSi to vertex VO. Here, if the silicon carboxide film at the coordinate point PO has (the number of atoms of) Si:C:O = a:b:c, α, β, and γ are expressed by the following formulas: - With reference to
FIG. 6A , the preferable composition ratio of a:b:c of the silicon carboxide film SiaCbOc as the liquid-repellent-layer base film 42A is described. Firstly, lines L1 to L6 on the triangular diagram showing composition of Si, C, and O are described. In the triangular diagram, the coordinate point corresponding to silicon dioxide SiO2 is PSiO2, the coordinate point corresponding to silicon carbide SiC is PSiC (P1), and the coordinate point corresponding to silicon dicarbide SiC2 is PSiC2 (P4). The line L1 is a line segment connecting the coordinate point PSiO2 and the coordinate point P1, and composite elements on the line L1 are SiC1-tO2t (0 ≤ t ≤ 1). The line L2 is a line segment connecting the coordinate point PSiO2 and the coordinate point P4, and composite elements on the line L2 are SiC2(1-s)O2s (0 ≤ s ≤ 1). The line L3 is a line segment connecting the coordinate point PSiO2 and the vertex VC. The line L4 is a line segment passing through the vertex VSi and satisfying b:c = 2:1. The line L5 is a line segment passing through the vertex VSi and satisfying b:c = 1:1. The line L6 is a line segment passing through vertex VSi and satisfying b:c = 1:2. - As described above, in terms of alkali resistance and chemical mechanical polishing resistance, it is preferable that the proportion of carbon be higher than the proportion of oxygen (c ≤ b). However, the liquid-repellent-
layer base film 42A at least needs to contain oxygen (c > 0) because hydroxy groups that react with a silane coupling agent as a liquid-repellent agent need to be present on the surface of the liquid-repellent-layer base film 42A when the liquid-repellent layer 43 is formed. Therefore, it is preferable that the ratio of carbon: oxygen (c/b) satisfy 0 < c/b ≤ 1. - As silicon oxide, silicon monoxide SiO and silicon dioxide SiO2 are known. Amorphous silicon oxide having an intermediate composition, namely SiOx where x < 2 stoichiometrically, also exists metastably. On the other hand, SiOx that satisfies 2 < x does not exist as a film because it is so-called peroxide and is unstable. Because hydroxy groups, which react with the silane coupling agent, need to exist on the surface of the liquid-repellent-
layer base film 42A when the liquid-repellent layer 43 is formed, the film at least needs to contain oxygen. Therefore, it is preferable that the ratio of silicon: oxygen (c/a) satisfy 0 < c/a ≤ 2. - With respect to the ratio of silicon: carbon, it is preferable that the proportion of carbon be larger than the line L1, and the proportion of silicon be larger than the line L2. Because silicon and carbon are both group 14 elements and have the same valence, substitution in the compound is possible. In terms of alkali resistance and chemical mechanical polishing resistance, it is preferable that the proportion of silicon and the proportion of carbon be around the same, or the proportion of carbon be larger than the proportion of silicon (1 ≤ b/a).
- However, the distance of a covalent bond formed by sp hybridized orbitals of a carbon atom is shorter than that of a covalent bond formed by sp hybridized orbitals of a silicon atom because the sp hybridized orbitals of a carbon atom are formed from 2s and 2p orbitals, whereas these of a silicon atom are formed from 3s and 3p orbitals. For that reason, the proportion of carbon being too high decreases adhesion between the
base part 41 and the liquid-repellent-layer base film 42A owing to the film stress of the liquid-repellent-layer base film 42A being larger. With respect to hydroxyl groups that react with the silane coupling agent when the liquid-repellent layer 43 is formed, because the electronegativity of silicon is smaller than that of carbon, the hydroxy groups bonded with silicon atoms (=Si-OH) have more localized charges than those bonded with carbon atoms (=C-OH), and hence have higher reactivity with the silane coupling agent. This is because the electronegativity of silicon is smaller than that of carbon. Therefore, the proportion of carbon needs to be limited (b/a ≤ 2). In consideration of this, the inventors believe it is preferable that the proportion of carbon be larger than the line L1 and the proportion of silicon be larger than the line L2. - Therefore, as shown in
FIG. 6A , the composition ratio of a:b:c of the silicon carboxide film SiaCbOc as the liquid-repellent-layer base film 42A is, according to the invention, in the triangular diagram, within a region enclosed with: the coordinate point P1 having the composition ratio of a:b:c = 1:1:0; the coordinate point P2 having the composition ratio of a:b:c = 3:2:2; the coordinate point P3 having the composition ratio of a:b:c = 1:2:2; and the coordinate point P4 having the composition ratio of a:b:c = 1:2:0, but not on a line segment connecting the coordinate point P1 and the coordinate point P4. - Next, an example of a method for producing the
nozzle substrate 40A in this embodiment is described with reference toFIGS. 7 to 8F .FIG. 7 is a flowchart showing a first nozzle substrate producing process.FIG. 8A is a schematic cross-sectional view of thebase part 41 before nozzle processing.FIG. 8B is a schematic cross-sectional view of thebase part 41 with the liquid-repellent-layer base film 42A formed.FIG. 8C is a schematic cross-sectional view of thebase part 41 with the liquid-repellent layer 43 formed.FIG. 8D is a schematic cross-sectional view of thebase part 41 with theprotective sheet 45 attached.FIG. 8E is a schematic cross-sectional view of thebase part 41 withnozzles 2411 formed.FIG. 8F is a schematic cross-sectional view of thenozzle substrate 40A with theprotective sheet 45 removed. - With reference to
FIG. 7 , the first nozzle substrate producing process for producing thenozzle substrate 40A is described. First, a manufacturer prepares abase part 41 as a base member as shown inFIG. 8A (Step ST11). Here, thebase part 41 is a polyimide (PI) film. The material of thebase part 41 can be resin, such as PET (PolyEthylene Terephthalate) or PPS (PolyPhenylene Sulfide). More specifically, Kapton film manufactured by DuPont, Upilex 75S manufactured by Ube Industries, TORELINA manufactured by TORAY, or the like may be used. Polyimide has high heat resistance, which enables annealing at a high temperature after the liquid-repellent-layer base film 42A is formed or after the liquid-repellent layer 43 is formed. PPS has high dimensional stability and can reduce variation in the length of nozzle rows of the inkjet heads 241. - As shown in
FIG. 8B , the manufacturer forms a silicon carboxide film having a composition ratio in the preferable range shown inFIG. 6A on the ejection surface side of thebase part 41 prepared in Step ST11, thereby forming the liquid-repellent-layer base film 42A (Step ST12). Use of the silicon carboxide film can produce the liquid-repellent-layer base film 42A having high alkali resistance and chemical mechanical polishing resistance. Because siloxane bonds can be formed, the liquid-repellent-layer base film 42A can have high fixability with the liquid-repellent agent. - In Step ST12, the silicon carboxide film can be formed using the following film-forming methods or the like.
- (1) High-frequency discharge plasma CVD (Chemical Vapor Deposition) or PIG (Penning Ionization Gauge) plasma CDV using: tetraethyl orthosilicate (TEOS); trimethylsilane (TMS); silane; hydrocarbon gas, such as methane, ethane, or acetylene; argon; oxygen gas; or the like
- (2) Sputtering using Si, SiC, or SiO2 as a target in an atmosphere of argon gas, oxygen gas, methane, or the like
- (3) Coating using a solution material containing silica (polysilazane system)
- As pretreatment of film formation of the liquid-repellent-
layer base film 42A in Step ST12, plasma treatment may be performed on thebase part 41. The plasma treatment can be performed with oxygen gas, argon gas, or a mixture of these gases. Performing the plasma treatment can bring about effects of decontaminating or activating the surface of thebase part 41 and improve adhesion between the liquid-repellent-layer base film 42A and thebase part 41. - As pretreatment of film formation of the liquid-repellent-
layer base film 42A in Step ST12, reverse sputtering treatment may be performed on thebase part 41. As the reverse sputtering treatment, sputtering is performed on thebase part 41 using oxygen gas, argon gas, or a mixture of these gases. Performing the reverse sputtering treatment can bring about effects of decontaminating or activating the surface of thebase part 41 and improve adhesion between the liquid-repellent-layer base film 42A and thebase part 41. - In the formation of the silicon carboxide film in Step ST12, the material gas may be hydrogenated. The hydrogenation may improve the stress, the film hardness, and the abrasion resistance of the silicon carboxide film.
- In Step ST12, the liquid-repellent-
layer base film 42A may be formed by firstly forming a silicon oxide film or a silicon carboxide film and secondly introducing carbon to the film surface thereof. As carbon introduction, plasma treatment with hydrocarbon gas, such as methane or ethane, can be used. As carbon introduction, an ion implantation method, an ion shower doping method, or the like can be used. When carbon is introduced to the surface of the liquid-repellent-layer base film, the profile of carbon in the composition ratio in the depth direction of the liquid-repellent-layer base film shows a tail from the surface of the base film. However, the composition ratio of the surface of the liquid-repellent-layer base film (outermost layer) can be controlled by carbonization to be a desirable composition ratio (within the preferable range shown inFIG. 6A ). - In Step ST12, in order to further improve fixability between the silicon carboxide film and the liquid-repellent agent, additional treatment, such as oxidation treatment during or after the film formation, may be performed so as to increase the number of siloxane bonding sites (-OH groups) on the surface of the silicon carboxide film. More specifically, examples of the additional treatment include: oxygenating the silicon carboxide film as the liquid-repellent-
layer base film 42A during the film formation thereof; and, after forming a silicon carbide film or the silicon carboxide film, oxidizing the surface thereof through oxygen plasma treatment or the like. - The above-described film formation methods and pretreatment methods of the liquid-repellent-
layer base film 42A may be appropriately combined, and are not limitations of the present invention. - It is preferable that the silicon carboxide film in Step ST12 be amorphous or monocrystalline. If the film is polycrystalline, the film may be selectively etched at crystal grain boundaries as etching sites and thereby have pinholes formed when immersed in an alkaline solution, and even the base material below may be etched. On the other hand, if the film is amorphous or monocrystalline, the film is not selectively etched even when immersed in the alkaline solution because there are no crystal grain boundaries as etching sites, so that the liquid-repellent-layer base film (flow channel protective film on the inner wall of nozzles) has higher alkali resistance.
- As shown in
FIG. 8C , the manufacturer forms the liquid-repellent layer 43 on the ejection surface side (front surface) of the liquid-repellent-layer base film 42A formed in Step ST12 (Step ST13). The liquid-repellent layer 43 may be formed by application or deposition of a silane coupling agent as the liquid-repellent agent having perfluoro carbon chains. As the silane coupling agent, OPTOOL manufactured by Daikin Industries, WR4 manufactured by Merck, FG-5080 and FG-5010 manufactured by FluoroTechnology, or the like may be used. - It is preferable that the formation of the liquid-repellent-
layer base film 42A in Step ST12 and the formation of the liquid-repellent layer 43 in Step ST13 be performed continuously without exposure thereof to air atmosphere. Avoidance of exposure to air atmosphere makes it possible to avoid decrease in adhesion between the layers, change in film quality, and so forth due to contamination of the interfaces of the layers. - As pretreatment of formation of the liquid-
repellent layer 43 in Step ST13, plasma treatment may be performed. The plasma treatment can be performed with oxygen gas, argon gas, or a mixture of these gases. Performing the plasma treatment can bring about effects of decontaminating or activating the surface of the liquid-repellent-layer base film 42A, improve reactivity and adhesion of the liquid-repellent-layer base film 42A to the liquid-repellent layer 43, and improve alkali resistance and chemical mechanical polishing resistance. A primer layer may be formed before the liquid-repellent layer 43 is formed in Step ST13. The formation of the primer layer can improve adhesion between the liquid-repellent layer 43 and the liquid-repellent-layer base film 42A. - As shown in
FIG. 8D , the manufacturer attaches aprotective sheet 45 to the ejection surface side (front surface) of the liquid-repellent layer 43 formed in Step ST13 (Step ST14). Theprotective sheet 45 has abase sheet 45a and anadhesive layer 45b on thebase sheet 45a. As thebase sheet 45a, polyimide, PET, PPS, or the like can be used. Theadhesive layer 45b is attached to the ejection surface side of the liquid-repellent layer 43. - As shown in
FIG. 8E , the manufacturer performs nozzle processing on the flow channel side (back surface) of thebase part 41, the liquid-repellent-layer base film 42A, and the liquid-repellent layer 43 to which theprotective sheet 45 is attached in Step ST14, thereby forming the nozzles 2411 (Step ST15). In Step ST15, the manufacturer irradiates the back surface of thebase part 41 with laser and forms thenozzles 2411. Use of the silicon carboxide film as the liquid-repellent-layer base film 42A makes it possible to accurately perform the laser processing on the liquid-repellent-layer base film 42A. - If the nozzle processing is performed using a KrF excimer laser as a laser light source in Step ST15, the wavelength of the KrF excimer laser is 248 nm, that is, the photon energy is 5.0 eV. When the silicon carboxide film is used as the liquid-repellent-
layer base film 42A, the band gap of the silicon carboxide film is narrower than that of SiO2 owing to the effect of carbon introduction (the band gap of SiO2 is 8-9 eV, and that of SiC is about 3 eV.). This improves absorption efficiency of a KrF excimer laser beam, allows the liquid-repellent-layer base film 42A to be ablated in nozzle processing, and restrains generation of burrs. Thus, processing accuracy of the edges of thenozzles 2411 is improved. - The thickness of the liquid-repellent-
layer base film 42A is preferably 100 nm or less, further preferably 50 nm or less, and still further preferably 20 nm or less. Laser ablation is performed easier on the liquid-repellent-layer base film 42A having a thinner film thickness, and less burrs are left. - With respect to the
adhesive layer 45b of theprotective sheet 45, the adhesive strength between theprotective sheet 45 and the surface of the liquid-repellent layer 43 should be between 0.1 and 0.7 N per 10 mm inclusive, and further preferably, between 0.15 and 0.64 N per 10 mm inclusive when theprotective sheet 45 and thebase part 41 are pulled apart in 180-degree opposite directions. Use of such anadhesive layer 45b makes it possible to perform nozzle processing without allowing theprotective sheet 45 to peel off from the surface of the liquid-repellent layer 43 through handling of work in laser processing. This can restrain generation of burrs or the like. - If the
base part 41 is made of metal material, such as SUS, and nozzle processing is performed using laser, it is preferable that a picosecond pulse laser be used as the laser light source. Use of a picosecond pulse laser makes it possible to prevent the metal from generating burrs and dross and form thenozzles 2411 having a good shape. - Then, as shown in
FIG. 8F , the manufacturer removes theprotective sheet 45 from thebase part 41, the liquid-repellent-layer base film 42A, the liquid-repellent layer 43, and theprotective sheet 45, in which thenozzles 2411 have been formed in Step ST15, thereby forming thenozzle substrate 40A (Step ST16), and ends the first nozzle substrate producing method. With respect to theadhesive layer 45b, the adhesive strength between theprotective sheet 45 and the surface of the liquid-repellent layer 43 should be between 0.1 and 0.7 N per 10 mm inclusive, or further preferably, between 0.15 and 0.64 N per 10 mm inclusive when theprotective sheet 45 and thebase part 41 are pulled apart in 180-degree opposite directions. Use of such anadhesive layer 45b makes it possible to remove theprotective sheet 45 without applying a stress, which can cause distortion of the dimensions of thebase part 41, to thebase part 41. - The manufacturer attaches the
nozzle substrate 40A, which has been formed by the first nozzle substrate producing process, to the pressure chamber substrate 50 (or the intermediate substrate), and forms a substrate in which thenozzle substrate 40A, the pressure chamber substrate 50, theoscillating plate 60, thespacer substrate 70, and thewiring substrate 80 are layered. The manufacturer then connects the substrate with a driving circuit, an ink supply channel(s), and so forth, and forms theinkjet head 241. Theinkjet head 241 is used as a part of theinkjet recording device 1. - As described above, according to this embodiment, the
inkjet head 241 includes thenozzle substrate 40A that includes: thebase part 41 in which thenozzles 2411 that eject ink are formed; the liquid-repellent-layer base film 42A that is formed on the ejection surface side of thebase part 41 and has the silicon carboxide film; and the liquid-repellent layer 43 that is formed on the ejection surface side of the liquid-repellent-layer base film 42A. - The liquid-repellent-
layer base film 42A as the silicon carboxide film makes it possible to improve reactivity with the liquid-repellent agent for forming the liquid-repellent layer 43 and resistance to ink, particularly alkaline ink, of thenozzle substrate 40A on the ejection surface side, thereby preventing decrease in liquid repellency of thenozzle substrate 40A on the ejection surface side. - Furthermore, according to the invention, the liquid-repellent-
layer base film 42A has the silicon carboxide film having a composition, in the triangular diagram showing the ratio of silicon Si, carbon C, and oxygen O in the number of atoms, within the range enclosed with: the first coordinate point at which the ratio of Si:C:O in the number of atoms is 1:1:0; the second coordinate point at which the ratio of SI:C:O in the number of atoms is 3:2:2; the third coordinate point at which the ratio of SI:C:O in the number of atoms is 1:2:2; and the fourth coordinate point at which the ratio of Si:C:O in the number of atoms is 1:2:0, but not on the line connecting the first coordinate point and the forth coordinate point. The liquid-repellent-layer base film 42A makes it possible, as shown in first and second examples to be described later, to obtain a high etching rate, greatly improve alkali resistance, and obtain a large contact angle, thereby improving liquid repellency. - Furthermore, the liquid-repellent-
layer base film 42A has a film thickness of 50 nm or less. This makes it possible to perform laser ablation easily in forming thenozzles 2411, and prevent burrs from being left on thebase part 41 and so forth. - Furthermore, the
base part 41 is made of silicon, metal material, or resin material. Use of silicon as thebase part 41 makes it possible to use photolithography or the like for nozzle processing. Such processing makes it possible to form thenozzles 2411 highly accurately and produce the inkjet heads 241 having few variations in ejection angles and high quality in image depiction. Use of polyimide, which is resin material, as thebase part 41 makes it possible to improve heat resistance and perform annealing at a high temperature after forming the liquid-repellent-layer base film 42A or the liquid-repellent layer 43. Use of PPS, which is resin material, as thebase part 41, can improve dimensional stability and reduce variations in nozzle length. Use of SUS, which is metal material, as thebase part 41 makes it possible to easily form thenozzles 2411 by punch processing, laser processing, or electroforming on the SUS film. - Furthermore, the
inkjet recording device 1 includes theinkjet head 241 that has thenozzle substrate 40A, and thecleaning unit 27 that wipes off ink on the ejection surface side of the liquid-repellent layer 43. This can restrain effects of chemical mechanical polishing due to ink wiping by thecleaning unit 27, and realize theinkjet recording device 1 that prevents decrease in liquid repellency of thenozzle substrate 40A on the ejection surface side. - Furthermore, the method for producing an inkjet head includes: a nozzle forming step of forming, in the
base part 41, thenozzles 2411 that eject ink; a liquid-repellent-layer base film forming step of forming the liquid-repellent-layer base film 42A that has the silicon carboxide film on the ejection surface side of thebase part 41; a liquid-repellent layer forming step of forming the liquid-repellent layer 43 on the ejection surface side of the liquid-repellent-layer base film 42A, thereby producing thenozzle substrate 40A; and an inkjet head producing step of producing theinkjet head 241 that includes thenozzle substrate 40A. - The liquid-repellent-
layer base film 42A made of the silicon carboxide film makes it possible to improve reactivity with the liquid-repellent agent for forming the liquid-repellent layer 43 and resistance to ink, particularly alkaline ink, of thenozzle substrate 40A on the ejection surface side, thereby preventing decrease of liquid repellency. - In the liquid-repellent-layer base film forming step, the liquid-repellent-
layer base film 42A of which outermost surface layer has a composition ratio in the range shown inFIG. 6A is formed by additional oxygenation on a silicon carbide film or a silicon carboxide film. Plasma treatment in an atmosphere containing oxygen gas is used as the oxygenation. This makes it possible to easily form the liquid-repellent-layer base film 42A as the silicon carboxide film having a composition ratio in the range shown inFIG. 6A . Thus, the number of siloxane bonding sites (-OH groups) on the surface of the silicon carboxide film can be increased, and fixability between the silicon carboxide film as the liquid-repellent-layer base film 42A and the liquid-repellent agent as the liquid-repellent layer 43 can be further improved. - Furthermore, in the liquid-repellent-layer base film forming step, the liquid-repellent-
layer base film 42A of which outermost surface layer has a composition ratio in the range shown inFIG. 6A is formed by additional carbon addition on a silicon oxide film or a silicon carboxide film. Plasma treatment in an atmosphere containing hydrocarbon gas is used as the carbon addition. This makes it possible to easily form the liquid-repellent-layer base film 42A as the silicon carboxide film having a composition ratio within the range shown inFIG. 6A . - Furthermore, in the nozzle forming step, after the liquid-repellent-
layer base film 42A is formed on thebase part 41 and the liquid-repellent layer 43 is formed thereon, thenozzles 2411 are formed by excimer laser processing ablating thebase part 41, the liquid-repellent-layer base film 42A, and the liquid-repellent layer 43. This makes it possible to perform laser ablation easily in the formation of thenozzles 2411, and prevent burrs from being left on thebase part 41 and so forth. - With reference to
FIGS. 9 to 11C , a first modification of the above embodiment is described. An inkjet recording device in this modification is configured as with the inkjet recording device I in the above embodiment, except that thenozzle substrate 40A is replaced with anozzle substrate 40B. The same part as the above embodiment is not described, and the part different from the above embodiment is mainly described. - With reference to
FIG. 9 , configuration of thenozzle substrate 40B is described.FIG. 9 is a schematic cross-sectional view of thenozzle substrate 40B. As shown inFIG. 9 , thenozzle substrate 40B includes abase part 41, a liquid-repellent-layer base film 42B, and a liquid-repellent layer 43. The liquid-repellent-layer base film 42B is provided on the ejection surface side of thebase part 41 and inside flow channels of thenozzles 2411. Part of the liquid-repellent-layer base film 42B constitutes a base layer of the liquid-repellent layer 43 on thebase part 41 side. In this modification, the liquid-repellent-layer base film 42B is a silicon carboxide film having a composition ratio in the preferable range shown inFIG. 6A . - Next, with reference to
FIGS. 10 to 11C , a method for producing thenozzle substrate 40B is described.FIG. 10 is a flowchart showing a second nozzle substrate producing process.FIG. 11A is a schematic cross-sectional view of thebase part 41 with thenozzles 2411 formed.FIG. 11B is a schematic cross-sectional view of thebase part 41 with the liquid-repellent-layer base film 42B formed.FIG. 11C is a schematic cross-sectional view of thenozzle substrate 40B with the liquid-repellent layer 43 formed. - With reference to
FIG. 10 , the second nozzle substrate producing process for producing thenozzle substrate 40B is described. First, as shown inFIG. 11A , the manufacturer performs nozzle processing on the flow channel side (back surface) of thebase part 41, thereby forming thebase part 41 as a base member with thenozzles 2411 formed (Step ST21). Herein, thebase part 41 is made of, for example, metal material (SUS). Thebase part 41 with thenozzle 2411 formed can be formed by, for example, forming on a SUS film depressed portions having a depth larger than the thickness of the SUS film through punch processing, and smoothing and polishing bulged portions formed on the back surface of the SUS film. Thebase part 41 with thenozzles 2411 formed can be also formed by performing laser processing on the SUS film and forming thenozzles 2411. Thebase part 41 made of metal material with thenozzles 2411 formed can be also formed by electroforming. - As shown in
FIG. 11B , the manufacturer forms a silicon carboxide film having a composition ratio in the preferable range shown inFIG. 6A on the ejection surface side (front surface) and the flow channel side (back surface) of thebase part 41 formed in Step ST21, thereby forming the liquid-repellent-layer base film 42B (Step ST22). By using the silicon carboxide film as the liquid-repellent-layer base film 42B in Step ST22, the surfaces of the liquid-repellent-layer base film and the flow channel protective film inside the flow channels can have high alkali resistance and chemical mechanical polishing resistance. Because siloxane bonds can be formed, the liquid-repellent-layer base film can have high fixability with the liquid-repellent agent. - In Step ST22, the silicon carboxide film can be formed, as with Step ST12 in
FIG. 7 , using the methods (1) to (3) or the like. As pretreatment of film formation of the liquid-repellent-layer base film 42B in Step ST22, plasma treatment may be performed on thebase part 41 as withStep ST 12 inFIG. 7 . Also, as pretreatment of film formation of the liquid-repellent-layer base film 42B, reverse sputtering treatment may be performed on thebase part 41. As the reverse sputtering treatment, sputtering is performed on the base using oxygen gas, argon gas, or a mixture of these gases. Performing the reverse sputtering treatment can bring about effects of decontaminating or activating the surface of thebase part 41 and improve adhesion between the liquid-repellent-layer base film 42B and thebase part 41. - In the formation of the silicon carboxide film in Step ST22, the material gas may be hydrogenated. The hydrogenation may improve the stress, the film hardness, and the abrasion resistance of the liquid-repellent-
layer base film 42B. In Step ST22, the liquid-repellent-layer base film 42A may be formed by firstly forming a silicon oxide film or a silicon carboxide film and secondly introducing carbon to the film surface thereof, as withStep ST 12 inFIG. 7 . In Step ST22, the liquid-repellent-layer base film 42B may be formed by: oxygenating a silicon carboxide film during film formation thereof; or, after forming a silicon carbide film or a silicon carboxide film, oxidizing the surface thereof as withStep ST 12 inFIG. 7 . - By forming the liquid-repellent-
layer base film 42B as a protective film on the inner walls of thenozzles 2411 and inside the flow channels in Step ST22, the flow channel protective film can have high alkali resistance and high lyophilic property. The silicon carboxide film, which has a high covalent bonding property and has hydroxy groups on the surface, is highly lyophilic (ink-philic, hydrophilic). This allows bubbles in the flow channels to easily escape when ink is introduced into theinkjet head 241, for example. Also, bubbles hardly adhere to the flow channels during operation of theinkjet head 241. Thus, ejection defects of thenozzles 2411 or the like are less likely to occur. - As shown in
FIG. 11C , the manufacturer forms the liquid-repellent layer 43 on the ejection surface side (front surface) of thebase part 41, on which the liquid-repellent-layer base film 42B has been formed in Step ST22, thereby forming thenozzle substrate 40B (Step ST23), and ends the second nozzle substrate producing method. In Step ST23, the liquid-repellent layer 43 is formed as with Step ST13 ofFIG. 7 . In Step ST23, it is possible to form the liquid-repellent layer 43 by: firstly forming a liquid-repellent layer on the ejection surface side (front surface), the inner walls of thenozzles 2411, and the flow channel side (back surface); and secondly removing all or part of the liquid-repellent layer on the inner walls of thenozzles 2411 and the flow channel side (back surface). As the removing method, plasma treatment, chemical treatment, or the like can be used. - In Step ST23, a liquid-repellent layer may be formed on the ejection surface side (front surface), the inner walls of the
nozzles 2411, and the flow channel side (back surface). Whereas the front surface of thenozzles 2411 contacts air, the inner walls of thenozzles 2411 and the inner walls of the flow channels are filled with ink, and no air is present. Therefore, the ink wettability of the inner walls of thenozzles 2411 and the inner walls of the flow channels may be lower than that of the front surface of thenozzles 2411. - As described above, according to this modification, the
nozzle substrate 40B of theinkjet head 241 has the liquid-repellent-layer base film 42B formed on the ejection surface side of thebase part 41 and the inner walls of thenozzles 2411. The liquid-repellent-layer base film 42B, which has high alkali resistance and high lyophilic property, can protect the ink flow channels. With the liquid-repellent-layer base film 42B, bubbles in the flow channels can easily escape when ink is introduced into theinkjet head 241, for example, and the bubbles hardly adhere to the flow channels during operation of theinkjet head 241. Thus, ejection defects of thenozzles 2411 or the like are less likely to occur. - With reference to FIG. 12A, a second modification of the above embodiment is described. An inkjet recording device in this modification is configured as with the
inkjet recording device 1 in the above embodiment, except that thenozzle substrate 40A is replaced with a nozzle substrate 40Ba. The same part as the above embodiment is not described, and the part different from the above embodiment is mainly described. - With reference to
FIG. 12 , configuration of the nozzle substrate 40Ba is described.FIG. 12 is a schematic cross-sectional view of the nozzle substrate 40Ba. - As shown in
FIG. 12 , the nozzle substrate 40Ba includes abase part 41, a liquid-repellent-layer base film 42A, a liquid-repellent layer 43, and a flow channelprotective film 44B. The flow channelprotective film 44B is provided on the ejection surface side of thebase part 41 and inside the flow channels of thenozzles 2411. Part of the nozzle substrate 40Ba constitutes a base layer (film) of the liquid-repellent-layer base film 42A on thebase part 41 side. The flow channelprotective film 44B is a protective film having ink resistance. - Next, a method for producing the nozzle substrate 40Ba is described. The method for producing the nozzle substrate 40Ba is the same as the producing method of the second nozzle substrate producing process in
FIG. 10 . However, after Step ST21 and before Step ST22 in the second nozzle substrate producing process, the manufacturer forms the flow channelprotective film 44B on the ejection surface side and the flow channel side of thebase part 41 with thenozzles 2411 formed in Step ST21. - As the flow channel
protective film 44B, a metal oxide film containing one or more kinds of metal elements that are chemically stable in a high oxidation state, such as tantalum, hafnium, niobium, titanium, and zirconium, may be used. Such a metal oxide film has high alkali resistance. As the flow channelprotective film 44, a metal silicate film may be used. The metal silicate film is a silicon-containing metal oxide film containing one or more kinds of metal elements that are chemically stable in a high oxidation state, such as tantalum, hafnium, niobium, titanium, and zirconium. Examples of such a metal silicate film include tantalum silicate, hafnium silicate, niobium silicate, titanium silicate, and zirconium silicate. The metal silicate film has alkali resistance, and also has a lower ionic bonding property and a higher covalent bonding property by containing silicon. This increases the number of hydroxy groups of the flow channelprotective film 44B and improves lyophilic property of the surface of the flow channelprotective film 44B. With the improved lyophilic property, bubbles in the flow channels easily escape when ink is introduced into theinkjet head 241, for example, and bubbles hardly adhere to the flow channels during operation of theinkjet head 241. Thus, ejection defects of thenozzles 2411 or the like are less likely to occur. - In Step ST22, instead of the liquid-repellent-
layer base film 42B, a liquid-repellent-layer base film 42A is formed on the ejection surface side of thebase part 41 with the flow channelprotective film 44B formed. For example, the liquid-repellent-layer base film 42A is formed by: forming a liquid-repellent-layer base film on the ejection surface side and the flow channel side of thebase part 41 with the flow channelprotective film 44B formed; attaching a protective sheet on the ejection surface side of thebase part 41 with the liquid-repellent-layer base film formed; removing the liquid-repellent-layer base film on the flow channel side through etching treatment or plasma treatment; and removing the protective sheet. Then, Step ST23 is performed and the nozzle substrate 40Ba is produced. - With reference to
FIGS. 13 to 15F , a third modification of the above embodiment is described. An inkjet recording device in this modification is configured as with theinkjet recording device 1 in the above embodiment, except that thenozzle substrate 40A is replaced with anozzle substrate 40C. The same part as the above embodiment is not described, and the part different from the above embodiment is mainly described. - With reference to
FIG. 13 , configuration of thenozzle substrate 40C is described.FIG. 13 is a schematic cross-sectional view of thenozzle substrate 40C. As shown inFIG. 13 , thenozzle substrate 40C includes abase part 41, a liquid-repellent-layer base film 42A, a liquid-repellent layer 43, and a flow channelprotective film 44. The flow channelprotective film 44 is provided on the ejection surface side of thebase part 41 and inside the flow channels of thenozzles 2411. Part of the flow channelprotective film 44 constitutes a base layer (film) of the liquid-repellent-layer base film 42A on thebase part 41 side. The flow channelprotective film 44 is a protective film having ink resistance. - Next, with reference to
FIGS. 14 to 15F , a method for producing thenozzle substrate 40C is described.FIG. 14 is a flowchart showing a third nozzle substrate producing process.FIG. 15A is a schematic cross-sectional view of thebase part 41C.FIG. 15B is a schematic cross-sectional view of thebase part 41C with the liquid-repellent-layer base film 42A formed.FIG. 15C is a schematic cross-sectional view of thebase part 41C withnozzle holes 2411a formed.FIG. 15D is a schematic cross-sectional view of thebase part 41C withink channels 2411b formed.FIG. 15E is a schematic cross-sectional view of thebase part 41C with the flow channelprotective film 44 formed.FIG. 15F is a schematic cross-sectional view of thenozzle substrate 40C with the liquid-repellent layer 43 formed. - With reference to
FIG. 14 , a third nozzle substrate producing process for producing thenozzle substrate 40C is described. In the producing process of thenozzle substrate 40C to be described as an example, thebase part 41 is thebase part 41C as an SOI (Silicon On insulator) substrate, and thenozzles 2411 arenozzles 2411C having nozzle holes and ink channels. - First, as shown in
FIG. 15A , the manufacturer prepares thebase part 41C as an SOI substrate (Step ST31). Thebase part 41C has a supportingsubstrate 41a, a BOX (Buried Oxide)layer 41b, and anSOI layer 41c that are layered in this order. Thebase part 41C as the SOI substrate can be formed using a substrate bonding method, an SIMOX (Separation by IMplantation of OXygen) method, an ELTRAN (Epitaxial Layer TRANsfer), or the like. The film thickness of theSOI layer 41c should be between 10 and 100 µm inclusive, and the film thickness of theBOX layer 41b should be between 50 and 200 nm inclusive. A silicon oxide film or the like may be formed on the surface of thebase part 41C, the surface being positioned on theSOI layer 41c side. - The thickness of the supporting
substrate 41a should be between 50 and 1,000 µm inclusive. Silicon may be used as the material of the supportingsubstrate 41a, although this is not a limitation. Quartz, glass, sapphire, SiC, GaN, YSZ, or the like may be used. Use of thebase part 41C having the supportingsubstrate 41a made of an ink-resistant material makes it possible to produce theinkjet head 241 of whichnozzles 2411C have highly ink-resistant inner walls and ink flow channels can be produced. - As shown in
FIG. 15B , the manufacturer forms a silicon carboxide film having a composition ratio in the preferable range shown inFIG. 6A on the ejection surface side (front surface) of theSOI layer 41c of thebase part 41C, which has been prepared in Step ST31, thereby forming the liquid-repellent-layer base film 42A (Step ST32). In Step ST32, the silicon carboxide film can be formed, as withStep ST 12 inFIG. 7 , using the methods (1) to (3) or the like. - As pretreatment of film formation of the liquid-repellent-
layer base film 42B in Step ST32, plasma treatment may be performed on thebase part 41 as withStep ST 12 inFIG. 7 . Also, as pretreatment of film formation of the liquid-repellent-layer base film 42B, reverse sputtering treatment may be performed on thebase part 41. In the formation of the silicon carboxide film in Step ST32, the material gas may be hydrogenated. In Step ST32, the liquid-repellent-layer base film 42B may be formed by firstly forming a silicon oxide film or a silicon carboxide film and secondly introducing carbon to the film surface thereof, as with Step ST12 inFIG. 7 . In Step ST32, the liquid-repellent-layer base film 42B may be formed by: oxygenating a silicon carboxide film during film formation thereof; or, after forming a silicon carbide film or a silicon carboxide film, oxidizing the surface thereof as withStep ST 12 inFIG. 7 . The above-described film formation methods and pretreatment methods may be appropriately combined, and are not limitations of the present invention. - As shown in
FIG. 15C , the manufacturer performs nozzle hole processing on the ejection surface side (front surface) of the liquid-repellent-layer base film 42A formed in Step ST32 and theSOI layer 41c of thebase part 41C, thereby formingnozzle holes 2411a (Step ST33). In Step ST33,nozzle holes 2411a are formed by, for example, applying a resist to the surface of the liquid-repellent-layer base film 42A, forming a resist pattern by exposure, and performing dry etching. As the dry etching, Bosch process or the like can be used. It is preferable that thenozzle holes 2411a be reversely tapered as viewed from the SOI layer surface side. Such a reversely tapered shape becomes a normally tapered shape as viewed from the flow channel side when nozzles are finished, and stabilizes meniscus vibration when ink droplets are ejected. This realizes theinkjet head 241 having excellent ejection characteristics. - As shown in
FIG. 15D , the manufacturer performs ink channel processing on the flow channel side (back surface) of the supportingsubstrate 41a and theBOX layer 41b of thebase part 41C, in which thenozzle holes 2411a have been formed in Step ST33 (Step ST34). In Step ST34, theink channels 2411b are formed by, for example, applying a resist to the back surface of the supportingsubstrate 41a, forming a resist pattern by exposure, and performing dry etching. Before theink channels 2411b are formed, the supportingsubstrate 41 a may be polished to make it thin so as to have the supportingsubstrate 41a of a desired size. - As shown in
FIG. 15E , the manufacturer forms a flow channelprotective film 44 on the flow channel side (back surface) of thebase part 41C with theink channels 2411b (nozzles 2411C) formed in Step ST34 (Step ST35). As the flow channelprotective film 44, a metal oxide film containing one or more kinds of metal elements that are chemically stable in a high oxidation state, such as tantalum, hafnium, niobium, titanium, and zirconium, may be used. Such a metal oxide film has high alkali resistance. As the flow channelprotective film 44, a metal silicate film may be used. The metal silicate film is a silicon-containing metal oxide film containing one or more kinds of metal elements that are chemically stable in a high oxidation state, such as tantalum, hafnium, niobium, titanium, and zirconium. Examples of such a metal silicate film include tantalum silicate, hafnium silicate, niobium silicate, titanium silicate, and zirconium silicate. Containing silicon, the metal silicate film, which has alkali resistance, has a low ionic bonding property and a high covalent bonding property. This increases the number of hydroxy groups of the flow channelprotective film 44B and improves lyophilic property of the surface of the flow channelprotective film 44B. With the improved lyophilic property, bubbles in the flow channels easily escape when ink is introduced into theinkjet head 241, for example, and bubbles hardly adhere to the flow channels during operation of theinkjet head 241. Thus, ejection defects of thenozzles 2411 or the like are less likely to occur. - A silicon carboxide film may be used as the flow channel
protective film 44. Use of the silicon carboxide film as the flow channelprotective film 44 can produce the flow channel protective film having high alkali resistance and high lyophilic property. The silicon carboxide film, which has a high covalent bonding property and has hydroxy groups on the surface, is highly lyophilic. This allows bubbles in the flow channels to easily escape when ink is introduced into theinkjet head 241, for example. Also, bubbles hardly adhere to the flow channels during operation of theinkjet head 241. Thus, ejection defects of the nozzles or the like are less likely to occur. A silicon carboxide film may be additionally layered on the whole of or part of the upper layer of the flow channelprotective film 44 made of the metal oxide or the metal silicate film. Thenozzle substrate 40C may not have the flow channelprotective film 44. - As shown in
FIG. 15F , the manufacturer forms a liquid-repellent layer on the ejection surface side (front surface) of thebase part 41C, on which the flow channelprotective film 44 has been formed in Step ST35, and the liquid-repellent-layer base film 42A, thereby forming thenozzle substrate 40C (Step ST36), and ends the third nozzle substrate producing method. In Step ST36, the liquid-repellent layer 43 is formed as with Step ST13 ofFIG. 7 . In Step ST36, it is possible to form the liquid-repellent layer 43 by: firstly forming a liquid-repellent layer on the ejection surface side (front surface), the inner walls of thenozzles 2411C, and the flow channel side (back surface); and secondly removing all or part of the liquid-repellent layer on the inner walls of thenozzles 2411C and the flow channel side (back surface). As the removing method, plasma treatment, chemical treatment, or the like can be used. - In Step ST36, a liquid-repellent layer may be formed on the ejection surface side (front surface), the inner walls of the
nozzles 2411C, and the flow channel side (back surface). Whereas the front surface of thenozzles 2411 C contacts air, the inner walls of thenozzles 2411C and the inner walls of the flow channels are filled with ink, and no air is present. Therefore, the ink wettability of the inner walls of thenozzles 2411C and the inner walls of the flow channels may be lower than that of the front surface of thenozzles 2411C. - As described above, according to this modification, the
nozzle substrate 40C of theinkjet head 241 includes the flow channelprotective film 44 formed inside the flow channels of thenozzles 2411. The flow channelprotective film 44 can protect the ink flow channels. Further, use of the silicon carboxide film as the flow channelprotective film 44 allows bubbles in the flow channel to easily escape when ink is introduced into theinkjet head 241, for example. Also, bubbles hardly adhere to the flow channels during operation of theinkjet head 241. Thus, ejection defects of thenozzles 2411 or the like are less likely to occur. - With reference to
FIG. 16 , (i) samples of silicon carboxide as a first example used as the liquid-repellent-layer base films FIG. 16 is a diagram showing coordinate points PSA and PSB of samples SA and SB, respectively, in the triangular diagram showing the ratio of Si:C:O in the number of atoms. - Firstly, the sample SA as an example of the silicon carboxide film SiaCbOc was produced. As pretreatment of film formation of the sample SA, O2 plasma treatment was performed on a base (Si wafer) by RIE-10NR manufactured by Samco. Conditions of the O2 plasma treatment were as follows: RF (Radio Frequency) power = 100 W; O2 flow rate = 60 sccm; and time = 20 sec.
- As the sample SA, a silicon carboxide film was formed on the base (Si wafer) using TEOS (TEtraethOxySilane) by a film forming apparatus (Plasma CVD apparatus PD-200ST manufactured by Samco). Conditions of the film formation were as follows: RF power = 500 W; RF frequency = 13.56 MHz; film formation pressure = 53 Pa; film formation temperature = 300°C; TEOS gas flow rate = 3 sccm; and Ar flow rate = 100 sccm.
- As an example of the silicon carboxide film SiaCbOc, the sample SB being a silicon oxide film was also produced. As with the sample SA, film formation pretreatment was performed on the base (Si wafer) of the sample SB. Then, a silicon carboxide film as the sample SB was formed on the base (Si wafer) using TEOS by the film forming apparatus (Plasma CVD apparatus PD-200ST manufactured by Samco). Conditions of the film formation were as follows: RF power = 400 W; RF frequency = 13.56 MHz; film formation pressure = 53 Pa; film formation temperature = room temperature; TEOS gas flow rate = 12 sccm; and O2 flow rate = 400 sccm.
- The composition ratio of Si, C, and O of each of the samples SA and SB was evaluated by an X-ray photoelectron spectrometer (QuanteraSXM manufactured by ULVAC-PHI). The composition ratio of the silicon carboxide film SiaCbOc as the sample SA was a:b:c = 32.5:39.7:27.8. The composition ratio of the silicon carboxide film SiaCbOc (silicon oxide film) as the sample SB was a:b:c = 58:0:42. As shown in
FIG. 16 , the coordinate points PSA and PSB corresponding to the samples SA and SB, respectively, are plotted in the triangular diagram showing the ratio of Si, C, and O in the number of atoms. The coordinate point PSA of the sample SA is included in the preferable range of the composition ratio of Si:C:O shown inFIG. 6A . The sample SB is a silicon oxide film, and the coordinate point PSB is not included in the same preferable range of composition ratio. - Next, the wet etching rate of each of the samples SA and SB that were immersed in an alkaline solution (aqueous potassium hydroxide solution) was evaluated. Followings are conditions of the evaluation experiment. As the etching conditions, 40% aqueous potassium hydroxide solution was used at 80°C. The etching rates were as shown in the table II below.
[Table II] SAMPLE NAME ETCHING RATE [nm/min] SAMPLE SA 0.11 SAMPLE SB 30.5 - As shown in the table II, the etching rate of the silicon carboxide film as the sample SA was about 1/300 of the etching rate of the silicon oxide film as the sample SB. This shows that the use of a silicon carboxide film like the sample SA as the liquid-repellent-
layer base films layer base films - With reference to
FIG. 17 , a second example of the above embodiment and the first and second modifications are described. More specifically, (i) samples of silicon carboxide used as the liquid-repellent-layer base films FIG. 17 is a diagram showing coordinate points and contact angles of samples S1 to S9, respectively, in the triangular diagram showing the ratio of Si:C:O in the number of atoms. - As with the first example, samples S1, S2, S3, S4, S5, S6, S7, S8, and S9 of the silicon carboxide film SiaCbOc having composition ratios shown in the table III below were produced.
[Table III] SAMPLE NAME COMPOSITION RATIO OF LIQUID-REPELLENT-LAYER BASE FILM CONTACT ANGLE [° ] Si C O STATIC RECEDING SAMPLE S1 1.00 0.00 0.00 SOAKED SOAKED SAMPLE S2 0.33 0.00 0.67 SOAKED SOAKED SAMPLE S3 0.58 0.00 0.42 37.9 9.2 SAMPLE S4 0.39 0.61 0.00 40.9 18.8 SAMPLE S5 0.39 0.59 0.02 63.7 44.5 SAMPLE S6 0.23 0.73 0.04 6.5 6.65 SAMPLE S7 0.38 0.56 0.06 70.6 52.4 SAMPLE S8 0.26 0.72 0.03 11.8 0 SAMPLE S9 0.28 0.42 0.30 77.8 63.1 - The sample S1 is silicon, the samples S2 and S3 are silicon oxide films, and the sample S4 is a silicon carbide film. As shown in
FIG. 17 , coordinate points PS1, PS2, PS3, PS4, PS5, PS6, PS7, PS7, PS8, and PS9 corresponding to the samples S1, S2, S3, S4, S5, S6, S7, S8, and S9, respectively, are plotted in the triangular diagram showing the ratio of SI:C:O in the number of atoms. - On each of the samples S1 to S9 as the liquid-repellent-
layer base films repellent layer 43 by application. Conditions of the application were as follows: the samples S1 to S9 were dipped in 0.1% OPTOOL solution for three minutes, and pulled up at a low speed (10 mm/sec); and ultrasonic cleaning (ultrasonic frequency 950 kHz for 20 minutes) was performed. - Next, each of the samples S1 to S9 with the liquid-repellent layer formed was immersed in an aqueous alkaline dummy ink having a pH of 11. Contact angles (static contact angle, receding contact angle) of the dummy ink were then measured to evaluate change in contact angles. The aqueous alkaline dummy ink having a pH of 11 was an aqueous solution in which a buffer solution of sodium carbonate, potassium carbonate, or the like was mixed with polypropylene glycol alkyl ether, dipolypropylene glycol alkyl ether, tripolypropylene glycol alkyl ether, or the like to adjust its pH to between 10 and 11 inclusive. The dummy ink to measure the contact angles was: diethylene glycol alkyl ether; triethylene glycol alkyl ether; tetraethylene glycol alkyl ether; polypropylene glycol alkyl ether; dipolypropylene glycol alkyl ether; tripolypropylene glycol alkyl ether; or a mixture of a plurality of solvents selected from these.
- The static contact angle and the receding contact angle of the dummy ink on each of the samples S1 to S9 with the liquid-repellent layer formed were as shown in the table III. In
FIG. 17 , the contact angles of each of the samples S1 to S9 are expressed by the size (diameter) of a circle centered at each of the coordinate points PS1 to PS9. Among the samples S1 to S9, the samples S5, S7, and S9 each having a composition ratio in the preferable range shown inFIG. 6A obtained preferable contact angles even in a deteriorated state after being immersed in the alkaline ink, and obtained preferable liquid repellency. - As the reasons why the resistance to alkaline ink increased, the following two reasons are considered.
- Firstly, it is considered that the increase in the number of hydroxy groups on the surface of the liquid-repellent-layer base film increased density of Si-O bonds formed between the compound forming the liquid-repellent layer and the liquid-repellent-layer base film, and consequently restrained the liquid-repellent material from desorbing from the liquid-repellent-layer base film, which is caused by alkaline hydrolysis.
- Secondly, it is considered that the improvement of alkali resistance of the liquid-repellent-layer base film restrained the liquid-repellent-layer base film from being etched during immersion in alkaline ink, and consequently restrained the liquid-repellent material from desorbing from the liquid-repellent-layer base film.
- The descriptions on the above embodiment and modifications are examples of a preferable inkjet head, an inkjet recording device, and a method for producing an inkjet head according to the present invention, and are not intended to limit the present invention.
- For example, at least two of the above embodiment and the modifications may be combined appropriately.
- Although the nozzle substrate described in the above embodiments and modifications is the nozzle substrate for a bend-mode inkjet head in which a plurality of substrates are layered, the present invention is not limited to this. For example, the nozzle substrate in the above embodiment and the modifications may be applied to a nozzle substrate of a shear-mode inkjet head that presses ink in channels by applying an electric field in a direction perpendicular to the poling direction of a piezoelectric element and shearing the piezoelectric element.
- As described above, an inkjet head, an inkjet recording device, and a method for producing an inkjet head in the present invention can be applied to image recording using ink.
-
- 1 inkjet recording device
- 10 medium supplying unit
- 11 medium supplying tray
- 12 conveying unit
- 121,122 roller
- 123 belt
- 20 image forming unit
- 21 image forming drum
- 221 claw part
- 222 drum
- 22 first delivering unit
- 23 temperature measuring unit
- 24 head unit
- 241 inkjet head
- 241a nozzle opening surface
- 2411, 2411C nozzle
- 2411 a nozzle hole
- 2411 b ink channel
- 242 inkjet module
- 243 first sub-tank
- 244 second sub-tank
- 245 fixing member
- 246 carriage
- 25 heating unit
- 26 second delivering unit
- 261,262,264 roller
- 263 belt
- 27 cleaning unit
- 271 wiping member
- 272 elastic member
- 273 unwinding roller
- 274 winding roller
- 30 medium receiving unit
- 31 medium receiving tray
- P recording medium
- 40A, 40B, 40Ba, 40C nozzle substrate
- 41, 41C base part
- 41a supporting substrate
- 41b BOX layer
- 41c SOI layer
- 42A, 42B liquid-repellent-layer base film
- 43 liquid-repellent layer
- 44, 44B flow channel protective film
- 45 protective sheet
- 45a base sheet
- 45b adhesive layer
- 50 pressure chamber substrate
- 51 pressure chamber
- 60 oscillating plate
- 70 spacer substrate
- 71 piezoelectric element part
- 80 wiring substrate
- R recording medium
Claims (16)
- An inkjet head (241) comprising a nozzle substrate (40A, 40B, 40Ba, 40C) that includes:a base part (41, 41C) in which a nozzle (2411, 2411C) that ejects ink is formed;a liquid-repellent-layer base film (42A, 42B) that is formed on an ejection surface side of the base part and includes a silicon carboxide film; anda liquid-repellent layer (43) that is formed on the ejection surface side of the liquid-repellent-layer base film,characterized in that the liquid-repellent-layer base film (42A, 42B) includes the silicon carboxide film having a composition ratio, in a triangular diagram showing a ratio of silicon Si, carbon C, and oxygen O in the number of atoms, within a range enclosed with: a first coordinate point (P1) at which the ratio of Si:C:O in the number of atoms is 1:1:0; a second coordinate point (P2) at which the ratio of Si:C:O in the number of atoms is 3:2:2; a third coordinate point (P3) at which the ratio of Si:C:O in the number of atoms is 1:2:2; and a fourth coordinate point (P4) at which the ratio of Si:C:O in the number of atoms is 1:2:0, but not on a line connecting the first coordinate point (P1) and the fourth coordinate point (P4).
- The inkjet head (241) according to claim 1, wherein the liquid-repellent-layer base film (42A, 42B) is formed on the ejection surface side of the base part (41, 41C) and an inner wall of the nozzle (2411, 2411C).
- The inkjet head (241) according to claim 1 or 2, further comprising a flow channel protective film (44, 44B) formed inside a flow channel (2411b) of the nozzle (2411, 2411C).
- The inkjet head (241) according to any one of claims 1 to 3, wherein the liquid-repellent-layer base film (42A, 42B) has a film thickness of 50 nm or less.
- The inkjet head (241) according to any one of claims 1 to 4, wherein the base part (41, 41C) is made of silicon, metal material, or resin material.
- An inkjet recording device (1) comprising:the inkjet head (241) according to any one of claims 1 to 5; anda cleaning unit (27) that wipes off the ink on the ejection surface side of the liquid-repellent layer (43).
- A method for producing an inkjet head (241), comprising:a liquid-repellent-layer base film forming step (ST12, ST22, ST32) of forming a liquid-repellent-layer base film (42A, 42B) that includes a silicon carboxide film on an ejection surface side of a base part (41, 41C);a liquid-repellent layer forming step (ST13, ST23, ST36) of forming a liquid-repellent layer (43) on the ejection surface side of the liquid-repellent-layer base film (42A, 42B), thereby producing a nozzle substrate (40A, 40B, 40Ba, 40C) ;a nozzle forming step (ST15, ST21, ST33) of forming, in the base part (41, 41C), a nozzle (2411, 2411C) that ejects ink; andan inkjet head producing step of producing an inkjet head (241) that includes the nozzle substrate (40A, 40B, 40Ba, 40C),characterized in that the liquid-repellent-layer base film (42A, 42B) includes the silicon carboxide film having a composition ratio, in a range in a triangular diagram showing a ratio of silicon Si, carbon C, and oxygen O in the number of atoms, within a range enclosed with: a first coordinate point (P1) at which the ratio of Si:C:O in the number of atoms is 1:1:0; a second coordinate point (P2) at which the ratio of Si:C:O in the number of atoms is 3:2:2; a third coordinate point (P3) at which the ratio of Si:C:O in the number of atoms is 1:2:2; and a fourth coordinate point (P4) at which the ratio of Si:C:O in the number of atoms is 1:2:0, but not on a line connecting the first coordinate point (P1) and the fourth coordinate point (P4).
- The method for producing an inkjet head (241) according to claim 7, wherein in the liquid-repellent-layer base film forming step (ST12, ST22, ST32), the liquid-repellent-layer base film (42A, 42B) of which outermost surface layer has the composition ratio in the range is formed by additional oxygenation on a silicon carbide film or the silicon carboxide film.
- The method for producing an inkjet head (241) according to claim 8, wherein plasma treatment in an atmosphere containing oxygen gas is used as the oxygenation.
- The method for producing an inkjet head (241) according to claim 7, wherein in the liquid-repellent-layer base film forming step (ST12, ST22, ST32), the liquid-repellent-layer base film (42A, 42B) of which outermost surface layer has the composition ratio in the range is formed by additional carbon addition on a silicon oxide film or the silicon carboxide film.
- The method for producing an inkjet head (241) according to claim 10, wherein plasma treatment in an atmosphere containing hydrocarbon gas is used as the carbon addition.
- The method for producing an inkjet head (241) according to any one of claims 7 to 11, wherein in the liquid-repellent-layer base film forming step (ST12, ST22, ST32), the liquid-repellent-layer base film (42A, 42B) is formed on the ejection surface side of the base part (41, 41C) and an inner wall of the nozzle (2411, 2411C).
- The method for producing an inkjet head (241) according to any one of claims 7 to 12, further comprising a flow channel protective film forming step (ST35) of forming a flow channel protective film (44, 44B) inside a flow channel (2411b) of the nozzle (2411, 2411C).
- The method for producing an inkjet head (241) according to any one of claims 7 to 13, wherein in the nozzle forming step (ST15, ST21, ST33), after the liquid-repellent-layer base film (42A, 42B) is formed on the base part (41, 41C) and the liquid-repellent layer (43) is formed thereon, the nozzle (2411, 2411C) is formed by excimer laser processing ablating the base part (41, 41C), the liquid-repellent-layer base film (42A, 42B), and the liquid-repellent layer (43).
- The method for producing an inkjet head (241) according to any one of claims 7 to 14, wherein in the liquid-repellent-layer base film forming step( ST12, ST22, ST32), the liquid-repellent-layer base film (42A, 42B) having a film thickness of 50 nm or less is formed.
- The method for producing an inkjet head (241) according to any one of claims 7 to 15, wherein the base part (41, 41C) is made of silicon, metal material, or resin material.
Applications Claiming Priority (2)
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JP2017134723 | 2017-07-10 | ||
PCT/JP2018/020648 WO2019012829A1 (en) | 2017-07-10 | 2018-05-30 | Inkjet head, inkjet recording device and method for producing inkjet head |
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EP3653386A1 EP3653386A1 (en) | 2020-05-20 |
EP3653386A4 EP3653386A4 (en) | 2020-07-08 |
EP3653386B1 true EP3653386B1 (en) | 2022-06-29 |
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EP18831247.4A Active EP3653386B1 (en) | 2017-07-10 | 2018-05-30 | Inkjet head, inkjet recording device and method for producing an inkjet head |
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EP (1) | EP3653386B1 (en) |
JP (1) | JPWO2019012829A1 (en) |
CN (1) | CN110869213B (en) |
WO (1) | WO2019012829A1 (en) |
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JP7384561B2 (en) * | 2019-02-18 | 2023-11-21 | ローム株式会社 | Nozzle substrate, inkjet print head and nozzle substrate manufacturing method |
JP7453760B2 (en) | 2019-08-08 | 2024-03-21 | キヤノン株式会社 | Substrate for liquid ejection head and method for manufacturing the same |
JP7485053B2 (en) | 2020-08-28 | 2024-05-16 | コニカミノルタ株式会社 | Nozzle plate and inkjet head |
JP2022078885A (en) | 2020-11-13 | 2022-05-25 | キヤノン株式会社 | Liquid ejection head substrate and liquid ejection head |
JP2022080444A (en) * | 2020-11-18 | 2022-05-30 | 東芝テック株式会社 | Inkjet head and inkjet printer |
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US3666460A (en) | 1966-01-11 | 1972-05-30 | Polaroid Corp | Diffusion transfer article and process using humectant in emulsion layer |
JP4784265B2 (en) * | 2005-11-01 | 2011-10-05 | 富士ゼロックス株式会社 | Droplet discharge device |
JP2007230061A (en) | 2006-02-28 | 2007-09-13 | Fujifilm Corp | Inkjet recording device |
JP5002290B2 (en) * | 2006-03-10 | 2012-08-15 | キヤノン株式会社 | Method for manufacturing liquid discharge head substrate |
KR20080004225A (en) * | 2006-07-05 | 2008-01-09 | 삼성전자주식회사 | Nozzle plate of inkjet head and method of manufacturing the nozzle plate |
JP2008062473A (en) * | 2006-09-06 | 2008-03-21 | Fuji Xerox Co Ltd | Liquid droplet ejection head, its manufacturing method and liquid droplet ejector |
JP2008149649A (en) * | 2006-12-20 | 2008-07-03 | Sharp Corp | Inkjet head and its manufacturing method |
JP5491909B2 (en) * | 2010-03-08 | 2014-05-14 | 富士フイルム株式会社 | Inkjet head manufacturing method |
JP2011194668A (en) * | 2010-03-18 | 2011-10-06 | Fujifilm Corp | Method for forming water repellent film, nozzle plate and ink jet head equipped with the same, and electronic device |
JP2013188874A (en) * | 2012-03-12 | 2013-09-26 | Fujifilm Corp | Method for manufacturing liquid ejection head |
JP2014069354A (en) * | 2012-09-27 | 2014-04-21 | Brother Ind Ltd | Manufacturing method of ink discharge head and the ink discharge head |
JP5594851B2 (en) * | 2012-09-27 | 2014-09-24 | 富士フイルム株式会社 | Film forming jig and film forming method using the film forming jig |
JP2014124880A (en) * | 2012-12-27 | 2014-07-07 | Seiko Epson Corp | Nozzle plate, liquid jet head, and liquid jet device |
US9205653B2 (en) * | 2014-01-23 | 2015-12-08 | Ricoh Company, Ltd. | Nozzle plate, liquid ejection head, and inkjet recording device |
-
2018
- 2018-05-30 WO PCT/JP2018/020648 patent/WO2019012829A1/en unknown
- 2018-05-30 EP EP18831247.4A patent/EP3653386B1/en active Active
- 2018-05-30 CN CN201880045420.8A patent/CN110869213B/en active Active
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EP3653386A1 (en) | 2020-05-20 |
CN110869213A (en) | 2020-03-06 |
CN110869213B (en) | 2022-04-19 |
WO2019012829A1 (en) | 2019-01-17 |
EP3653386A4 (en) | 2020-07-08 |
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