MEDIA TRANSPORTS
20190248159 ยท 2019-08-15
Assignee
Inventors
Cpc classification
B41J11/0085
PERFORMING OPERATIONS; TRANSPORTING
B41J11/007
PERFORMING OPERATIONS; TRANSPORTING
International classification
B41J11/00
PERFORMING OPERATIONS; TRANSPORTING
Abstract
An ink jet media transport that includes a polyalkylene furandicarboxylate layer substrate with a coating layer of a mixture of a conductive component and a polymer.
Claims
1. An ink jet media transport belt comprising a polyalkylene furandicarboxylate substrate layer having a surface and a coating layer on the surface of the polyalkylene furandicarboxylate substrate layer, the coating layer comprising a mixture of a conductive component and a polymer.
2. The belt of claim 1 wherein said conductive component is selected from the group consisting of carbon black, graphite, carbon nanotubes, fullerene, graphene, metal oxides, mixed metal oxides, and mixtures thereof.
3. The belt of claim 1 wherein said polyalkylene furandicarboxylate is bio-based polyethylene furandicarboxylate.
4. The belt of claim 1 wherein the belt exhibits a surface resistivity of from about 10.sup.1 /square to about 10.sup.6 /square as measured by a Resistance Meter.
5. (canceled)
6. The belt of claim 1 wherein said coating layer is of a thickness of from about 5 microns to about 30 microns.
7. The belt of claim 1 wherein said substrate layer is of a thickness of from about 25 microns to about 150 microns.
8. The belt of claim 1 wherein said polyalkylene furandicarboxylate substrate layer is in direct contact with said coating layer.
9. The belt of claim 1 wherein said polyalkylene furandicarboxylate is polyethylene furandicarboxylate.
10. The belt of claim 1 wherein said conductive component is carbon black.
11. An ink jet media system comprising the belt of claim 1, and further comprising a print zone, a plurality of ink jet print heads with face plates, a reservoir that supplies ink compositions to said ink jet print heads, rollers in contact with the belt, an ink jet sensor, and a vacuum plenum in contact with a platen.
12. (canceled)
13. The belt of claim 1 wherein the belt is a seamed belt.
14. (canceled)
15. (canceled)
16. (canceled)
17. (canceled)
18. (canceled)
19. The belt of claim 1 wherein said alkylene of the polyalkylene furandicarboxylate substrate layer contains from 2 carbon atoms to about 18 carbon atoms.
20. The belt of claim 1 wherein said polyalkylene furandicarboxylate has the following Formula ##STR00002## where n represents the number of repeating segments, and is from about 50 to about 1,500.
21. The belt of claim 20 wherein said n is from about 100 to about 500.
22. The belt of claim 1 wherein said polymer is a polyester.
23. The belt of claim 1 wherein said polyalkylene furandicarboxylate is a copolymer selected from the group consisting of polyethylene furandicarboxylate terephthalate, polypropylene furandicarboxylate terephthalate, and polybutylene furandicarboxylate terephthalate.
24. (canceled)
25. (canceled)
26. (canceled)
27. (canceled)
28. The belt of claim 1, wherein the polyalkylene furandicarboxylate is polyethylene furandicarboxylate, the conductive component is carbon black, and the polymer is a polyester.
29. The belt of claim 28, wherein the polyethylene furandicarboxylate has the following Formula ##STR00003## where n represents the number of repeating segments, and is from about 50 to about 1,500.
30. The belt of claim 29, wherein the polyester is a copolyester of ethylene glycol, diethylene glycol, terephthalic acid and isophthalic acid.
31. The belt of claim 1, wherein the coating layer comprises from about 30 weight percent to about 70 weight percent of the conductive component and from about 30 weight percent to about 70 weight percent of the polymer.
32. The belt of claim 31, wherein the polyalkylene furandicarboxylate is polyethylene furandicarboxylate, the conductive component is carbon black, and the polymer is a polyester.
33. The belt of claim 32, wherein the polyethylene furandicarboxylate has the following Formula ##STR00004## where n represents the number of repeating segments, and is from about 50 to about 1,500.
34. The belt of claim 33, wherein the polyester is a copolyester of ethylene glycol, diethylene glycol, terephthalic acid and isophthalic acid.
35. The belt of claim 31, wherein the conductive component and the polymer are present at about the same amount.
36. The belt of claim 1, wherein the coating layer consists of the conductive component; the polymer; optionally, a plasticizer; and optionally, a leveling agent.
37. The belt of claim 36, wherein the belt consists of the substrate layer and the coating layer.
38. The belt of claim 28, wherein the coating layer consists of the conductive component; the polymer; optionally, a plasticizer; and optionally, a leveling agent.
39. The belt of claim 31, wherein the coating layer consists of the conductive component; the polymer; optionally, a plasticizer; and optionally, a leveling agent.
Description
FIGURES
[0023] The following Figures are provided to illustrate, for example, ink jet systems and media transports comprising a substrate, and thereover a partially conductive coating. In these Figures and with respect to the present disclosure, media refers, for example, to coated or uncoated papers, films, parchments, transparencies, plastics, fabrics, photo-finishing papers, and the like, upon which information including text, images, or both can be reproduced.
[0024] Illustrated in
[0025]
[0026]
[0027]
[0028]
EMBODIMENTS
[0029] There is illustrated in
[0030] Belt 108, whether seamed or seamless, where seamless belts can be generated by know methods, reference for example U.S. Pat. No. 6,106,762, the disclosure of which is totally incorporated herein by reference, is formed as an endless loop as illustrated in
[0031] During operation of the system 100, the engagement of belt 108 enables media like paper, not shown, placed on the belt 108 to move toward the print zone 104 where tiny droplets of ink are sprayed onto the media in a controlled manner for the purpose of printing a desired image or text onto the media passing by. The ink jet print heads are mounted such that their faces, where ink nozzles are located, are spaced at, for example, about 1 millimeter or less from the media surface. Since media, such as paper, may possess a curl property that lifts at least a portion of the media more than, for example, at least about 1 millimeter above the surface of transport belt 108, minimizing or avoiding contact between the media to one of the print heads in print zone 104 can be desirable, and is achievable by, for example, known decurling devices.
[0032] With further reference to
[0033] To control, that is increase or decrease the 108 belt tension, and to minimize unnecessary drag to the belt, there can be increased the spacing between the rollers, like rollers R2 and R6, and this also assists in maintaining the desired registration speed of the media transport belt.
[0034] Additionally, the media transport belt 108 may be totally, that is 100 percent opaque, to for example, avoid interference with a belt speed sensing device, not shown, that determines and controls the speed, from left to right relative to
[0035] Also, shown in
[0036] The inner surfaces 200 of the media transport belt 108, shown in
[0037] Roller R4, shown in
[0038] In
[0039]
[0040]
[0041]
[0042] Media Transport Components
[0043] The media transport comprises, for example, a transport belt, inclusive of a seamed vacuum transport belt, or a transport belt free of seams, and further including a platen for supporting the belt. In embodiments, the disclosed belt comprises a conductive coating, or partially conductive coating in contact with a polyalkylene furandicarboxylate substrate, and where the coating comprises a polymer, such as a polyester and a conductive component, and which coating also includes as optional components at least one plasticizer and at least one leveling agent.
[0044] Polymer Examples
[0045] Various mixtures of at least one conductive component and at least one polymer can be selected for the disclosed media transport member coatings, such as those members in the configuration of a belt.
[0046] Examples of polymers that can be selected for the coating mixture include thermoplastics, polycarbonates, polysulfones, polyesters, such as aliphatic polyesters of, for example, polyglycolic acids, polylactic acids, and polycaprolactones, and aliphatic copolyesters, such as polyethylene adipates and polyhydroxyalkanoates. Specific examples of polyesters selected for the transport media coating mixture or layer are, for example, VITEL 1200B (T.sub.g=69 C., M.sub.w=45,000, a copolyester prepared from ethylene glycol, diethylene glycol, terephthalic acid, and isophthalic acid), 3300B (T.sub.g=18 C., M.sub.w=63,000), 3350B (T.sub.g=18 C., M.sub.w=63,000), 3200B (T.sub.g=17 C., M.sub.w=63,500), 3550B (T.sub.g=11 C., M.sub.w=75,000), 3650B (T.sub.g=10 C., M.sub.w=73,000), 2200B (T.sub.g=69 C., M.sub.w=42,000, a copolyester prepared from ethylene glycol, diethylene glycol, neopentyl glycol, terephthalic acid, and isophthalic acid), and 2300B (T.sub.g=69 C., M.sub.w=45,000), all available from Bostik Incorporated headquartered in Milwaukee, Wis.
[0047] Examples of polyesters 30, included in the coating mixture, include aromatic polyester copolymers, such as VITEL 1200B (Tg=69 C.; M.sub.w=45,000), 3300B (Tg=18 C.; M.sub.w=63,000, a co-polyester prepared from ethylene glycol, diethylene glycol, terephthalic acid, and isophthalic acid), 3350B (Tg=18 C.; M.sub.w=63,000), 3200B (Tg=17 C.; M.sub.w=63,500), 3550B (Tg=minus 11 C.; M.sub.w=75,000), 3650B (Tg=minus 10 C.; M.sub.w=73,000), 2200B (Tg=69 C.; M.sub.w=42,000, a co-polyester prepared from ethylene glycol, diethylene glycol, neopentyl glycol, terephthalic acid, and isophthalic acid), and 2300B (Tg=69 C.; M.sub.w=45,000), all these polyesters being commercially available from Bostik Incorporated headquartered in Milwaukee, Wis.
[0048] The disclosed glass transition temperatures (T.sub.g) can be determined by a number of known methods, and more specifically, such as by Differential Scanning calorimetry (DSC). For the disclosed molecular weights, such as M.sub.w (weight average) and M.sub.n (number average), they can be measured by a number of known methods, and more specifically, by Gel Permeation Chromatography (GPC).
[0049] The polymer can be present in the mixture in a number of differing effective amounts, such as for example, from about 30 weight percent to about 99 weight percent, in those situations when other optional components, such as plasticizers and leveling agents may not be present, from about 60 weight percent to about 97 weight percent, from about 70 weight percent to about 95 weight percent, from about 75 weight percent to about 92 weight percent, or from about 80 weight percent to about 87 weight percent of the total solids, and providing the total percent of components present is about 100 percent.
[0050] Conductive Component Examples
[0051] Examples of conductive components selected for the coating mixture include known carbon forms like carbon black, graphite, carbon nanotube, fullerene, graphene, and the like; metal oxides, mixed metal oxides, and mixtures thereof; polymers that have conductive characteristics, such as polyaniline, polythiophene, polypyrrole, mixtures thereof, and the like.
[0052] Examples of carbon black conductive components that can be selected for incorporation into the media transport coating layer illustrated herein include KETJENBLACK carbon blacks, available from AkzoNobel Functional Chemicals, Special Black 4 (B.E.T. surface area=180 m.sup.2/g, DBP absorption=1.8 ml/g, primary particle diameter=25 nanometers), available from Evonik-Degussa, Special Black 5 (B.E.T. surface area=240 m.sup.2/g, DBP absorption=1.41 ml/g, primary particle diameter=20 nanometers), Color Black FW1 (B.E.T. surface area=320 m.sup.2/g, DBP absorption=2.89 ml/g, primary particle diameter=13 nanometers), Color Black FW2 (B.E.T. surface area=460 m.sup.2/g, DBP absorption=4.82 ml/g, primary particle diameter=13 nanometers), Color Black FW200 (B.E.T. surface area=460 m.sup.2/g, DBP absorption=4.6 ml/g, primary particle diameter=13 nanometers), all available from Evonik-Degussa; VULCAN carbon blacks, REGAL carbon blacks, MONARCH carbon blacks, EMPEROR carbon blacks, and BLACK PEARLS carbon blacks available from Cabot Corporation. Specific examples of conductive carbon blacks are BLACK PEARLS 1000 (B.E.T. surface area=343 m.sup.2/g, DBP absorption=1.05 ml/g), BLACK PEARLS 880 (B.E.T. surface area=240 m.sup.2/g, DBP absorption=1.06 ml/g), BLACK PEARLS 800 (B.E.T. surface area=230 m.sup.2/g, DBP absorption=0.68 ml/g), BLACK PEARLS L (B.E.T. surface area=138 m.sup.2/g, DBP absorption=0.61 ml/g), BLACK PEARLS 570 (B.E.T. surface area=110 m.sup.2/g, DBP absorption=1.14 ml/g), BLACK PEARLS 170 (B.E.T. surface area=35 m.sup.2/g, DBP absorption=1.22 ml/g), EMPEROR 1200, EMPEROR1600, VULCAN XC72 (B.E.T. surface area=254 m.sup.2/g, DBP absorption=1.76 ml/g), VULCAN XC72R (fluffy form of VULCAN XC72), VULCAN XC605, VULCAN XC305, REGAL 660 (B.E.T. surface area=112 m.sup.2/g, DBP absorption=0.59 ml/g), REGAL 400 (B.E.T. surface area=96 m.sup.2/g, DBP absorption=0.69 ml/g), REGAL 330 (B.E.T. surface area=94 m.sup.2/g, DBP absorption=0.71 ml/g), MONARCH 880 (B.E.T. surface area=220 m.sup.2/g, DBP absorption=1.05 ml/g, primary particle diameter=16 nanometers), and MONARCH 1000 (B.E.T. surface area=343 m.sup.2/g, DBP absorption=1.05 ml/g, primary particle diameter=16 nanometers); special carbon blacks available from Evonik Incorporated; and Channel carbon blacks, available from Evonik-Degussa. Other known suitable carbon blacks not specifically disclosed herein may be selected as the conductive component.
[0053] Examples of polyaniline conductive components that can be selected for incorporation into the coating mixture are PANIPOL F, commercially available from Panipol Oy, Finland; and known lignosulfonic acid grafted polyanilines. These polyanilines usually have a relatively small particle size diameter of, for example, from about 0.5 micron to about 5 microns; from about 1.1 microns to about 2.3 microns, or from about 1.5 microns to about 1.9 microns.
[0054] Metal oxide conductive components that can be selected for the disclosed coating mixture include, for example, tin oxide, antimony doped tin oxide, indium oxide, indium tin oxide, zinc oxide, titanium oxide, mixtures thereof, and the like. Mixed metal oxides include, for example, tin oxide and antimony doped tin oxide, tin oxide and indium oxide, tin oxide and zinc oxide, antimony doped tin oxide and indium tin oxide, zinc oxide and titanium oxide, titanium oxide and tin oxide, antimony doped tin oxide, zinc oxide and titanium oxide, indium oxide, titanium oxide, and tin oxide, antimony doped tin oxide, indium oxide, and titanium oxide, mixtures thereof, and the like.
[0055] The conductive component amount is, for example, from about 1 weight percent to about 70 weight percent, from about 3 weight percent to about 40 weight percent, from about 5 weight percent to about 30 weight percent, from about 8 weight percent to about 25 weight percent, or from about 13 weight percent to about 20 weight percent of the total solids, and providing the total percent of solids present is about 100 percent.
[0056] The conductive layer mixture or coating layer can be included in a number of thicknesses, such as for example from about 0.1 micron to about 50 microns, from about 1 micron to about 40 microns, from about 5 microns to about 30 microns, or from about 10 microns to about 15 microns.
[0057] The conductive layer mixture or coating layer can be included in a number of thicknesses, such as for example from about 0.1 micron to about 50 microns, from about 1 micron to about 40 microns, from about 5 microns to about 30 microns, or from about 10 microns to about 15 microns.
[0058] Optional Plasticizers
[0059] Optional plasticizers that primarily function to increase the plasticity or fluidity of a material, like the polymer selected for the disclosed media transport member conductive coating mixture, include diethyl phthalate (DEP), dioctyl phthalate, diallyl phthalate, polypropylene glycol dibenzoate, di-2-ethyl hexyl phthalate, diisononyl phthalate, di-2-propyl heptyl phthalate, diisodecyl phthalate, di-2-ethyl hexyl terephthalate, other known suitable plasticizers, mixtures thereof, and the like. The plasticizers, which can be present in various effective amounts, such as for example, from about 0.1 weight percent to about 30 weight percent, from about 1 weight percent to about 20 weight percent, or from about 3 weight percent to about 15 weight percent based on the solids, and providing that the total amount of solids present is equal to about 100 percent.
[0060] Optional Leveling Agents
[0061] Optional leveling agent examples selected for the coating mixture media transport members, which agents can contribute to the smoothness characteristics, such as enabling smooth coated surfaces with minimal or no blemishes or protrusions of the members illustrated herein include, for example, polysiloxane polymers. The optional polysiloxane polymers selected include, for example, a polyester modified polydimethylsiloxane with the tradename of BYK 310 (about 25 weight percent in xylene) and BYK 370 (about 25 weight percent in xylene/alkylbenzenes/cyclohexanone/monophenylglycol=75/11/7/7); a polyether modified polydimethylsiloxane with the tradename of BYK 333, BYK 330 (about 51 weight percent in methoxypropylacetate) and BYK 344 (about 52.3 weight percent in xylene/isobutanol=80/20), BYK-SILCLEAN 3710 and 3720 (about 25 weight percent in methoxypropanol); a polyacrylate modified polydimethylsiloxane with the tradename of BYK-SILCLEAN 3700 (about 25 weight percent in methoxypropylacetate); or a polyester polyether modified polydimethylsiloxane with the tradename of BYK 375 (about 25 weight percent in di-propylene glycol monomethyl ether), all commercially available from BYK Chemical of Wesel, Germany, mixtures thereof, and the like. The leveling agents for the conductive coating mixture are selected in various effective amounts, such as for example, from about 0.01 weight percent to about 5 weight percent, from about 0.1 weight percent to about 3 weight percent, and from about 0.2 weight percent to about 1 weight percent based on the solids present, and providing that the total amount of solids present is equal to about 100 percent.
[0062] Optional Silicas
[0063] Optional silica examples present in the disclosed media transport member coating mixture, and which silicas can contribute to the wear resistant properties of the member include silica, fumed silicas, surface treated silicas, other known silicas, such as AEROSIL R972, mixtures thereof, and the like. The silicas are selected in various effective amounts, such as for example, from about 0.1 weight percent to about 20 weight percent, from about 1 weight percent to about 15 weight percent, and from about 2 weight percent to about 10 weight percent based on the solids, and providing that the total amount of solids present is equal to about 100 percent.
[0064] Optional Fluoropolymer Particles
[0065] Optional fluoropolymer particles selected for the disclosed conductive mixture media transport member, and which particles can contribute to the wear resistant properties of the members illustrated herein, include tetrafluoroethylene polymers (PTFE), trifluorochloroethylene polymers, hexafluoropropylene polymers, vinyl fluoride polymers, vinylidene fluoride polymers, difluorodichloroethylene polymers, or copolymers thereof. The fluoropolymer particles are selected in various effective amounts, such as for example, from about 0.1 weight percent to about 20 weight percent, from about 1 weight percent to about 15 weight percent, and from about 2 weight percent to about 10 weight percent based on the solids, and providing that the total amount of solids present is equal to about 100 percent.
[0066] Substrate Examples
[0067] The disclosed media transport, such as a media belt that functions primarily as a supporting substrate for the disclosed coating mixture, comprises at least one of a polyalkylene furandicarboxylate, such as a bio-based polyalkylene furandicarboxylate generated, for example, from renewal sources, where alkylene contains, for example, from about 1 carbon atom to about 50 carbon atoms, from about 2 carbon atom to about 18 carbon atoms, from about 2 carbon atoms to about 12 carbon atoms, from about 2 carbon atoms to about 6 carbon atoms, or from about 5 carbon atoms to about 25 carbon atoms.
[0068] Examples of polyalkylene furandicarboxylates include polyethylene furandicarboxylate (PEF), polyethylene 2,5-furandicarboxylate, polypropylene furandicarboxylate (PPF), polybutylene furandicarboxylate (PBF), polyalkylene furancarboxylates copolymers of polyethylene furandicarboxylate terephthalate, polypropylene furandicarboxylate terephthalate, polybutylene furandicarboxylate terephthalate, mixtures thereof, and the like, all believed to be available from Avantium Research Institute of Amsterdam Netherlands, and Toyobo Company Ltd. of Japan, and also available from the joint efforts of Avantium Research Institute of Amsterdam Netherlands and Toyobo Company Ltd. of Japan, and from the Stanford University Labs, or prepared as disclosed herein.
[0069] It is believed that the disclosed polyalkylene furandicarboxylates (PEF), inclusive of bio-based polyalkylene furandicarboxylates, can be prepared as illustrated in the Journal of Energy and Environmental Science Issue 4, 2012 titled Replacing Fossil Based PET with Bio-based PEF, listed authors A.J.J.E. Eerhart, and M. K. Patel, the disclosure of which is totally incorporated herein by reference; European Polymer Journal, Volume 83, October 2016, Pages 202-229, listed authors of George Z Papageorgiou, Dimitrios G. Papageorgiou, Zoi Terzopoulou, and Dimitrios N. Bikiaris, the disclosure of which is totally incorporated herein by reference; and Nature 531, News and Views, Sustainable Chemistry: Putting Carbon Dioxide to Work, Mar. 9, 2016, listed author Eric J. Beckman, the disclosure of which is totally incorporated herein by reference. Compared with known polyethylene terephthalate (PET) substrates, polyalkylene furandicarboxylates, such as polyethylene furandicarboxylates, can be prepared from 100 percent renewable sources, from substances derived from living or once-living organisms, such as renewable domestic agricultural products like plants, animal and marine substances, or forestry substances including biomass mixtures, soybeans, corn, flax, jute, and the like thus permitting a reduction in the carbon footprint by at least 50 percent.
[0070] In a known specific process to obtain PEF, fructose derived from plants is converted by way of a four-step process to furan-2,5-dicarboxylic acid (FDCA), which can then be reacted with ethylene glycol. The FDCA can also be prepared by reacting 2-furan carboxylate (FC) with carbon dioxide in the presence of cesium carbonate (Cs.sub.2CO.sub.3).
[0071] The polyalkylene furandicarboxylate substrate can be of a number of different thicknesses, such as from about 25 microns to about 250 microns, from about 25 microns to about 150 microns, about 50 microns to about 125 microns, or from about 75 microns to about 150 microns, and where the total thickness of the belt is, for example, from about 1 to about 10 mils, from about 1 to about 8 mils, from about 1 mil to about 5 mils, from about 2 mils to about 4 mils, and more specifically, about 3.8 mils, measured by known means such as a Permascope.
[0072] A polyalkylene furandicarboxylate polymer, such as polyethylene furan-2,5-dicarboxylate selected for the media transport coating mixture supporting substrate, can be represented by the following formula/structure
##STR00001##
with n representing the number of repeating segments, and which n can be, for example, of a value of from about 50 to about 1,500, from about 100 to about 800, or from about 100 to about 500.
[0073] Media Transport Preparation
[0074] The media transport in the form of a sheet can be converted into, for example, a media transport belt by a number of suitable processes, such as by known welding processes. For example, an elongated strip of the media belt material, in various suitable sizes, which belt is comprised of the coating mixture illustrated herein supported by the polyalkylene furandicarboxylate substrate illustrated herein, was cut longitudinally along opposite edge margins of the belt material, to produce an about 4552 millimeters wide elongated strip followed by slitting longitudinally along opposite edge margins of the strip, to produce an about 4402 millimeters wide coated elongated strip of belt material, and after removal of the coating from the edge margins of the elongated strip of the belt material, there can be generated uncoated edge margins as shown in
[0075] Thereafter, with a commercially available edge offset reduction system of a high resolution camera, the output of which provides feedback control to a motor that adjusts the edge margins of the endless looped belt such that they do not greatly vary from each other relative to a longitudinal centerline by more than about 3002 m (micrometers), can be used to minimize any endless loop irregularities, such as conicity, that is any conic shaped irregularity throughout the entire circumference of the belt.
[0076] Subsequently, the overlapped end portions of the belt are permanently joined via ultrasonic welding to produce a seamed belt, also characterized as a closed circular loop, measuring, for example, about 6552 millimeters in diameter by about 4402 millimeters wide. There can be selecting for the welding process commercially available Branson ultrasonic welding equipment, which permits the continuously joining of the opposite end portions of the media transport belt to produce an overlapped seam. Specifically, to facilitate joining together the two ends of the substrate of, for example, substrate 15, coating material trapped between end layers of the substrate material can be heated to a liquid state during the welding process, and forced out of the overlap area thereby resulting in an excellent weld. The seam break strength as measured by an Instron Universal Tester can be greater than about 50 pounds per inch, and more specifically, from about 75 pounds per inch to about 125 pounds per inch. Any materials forced out from the overlap weld area can then be removed from the belt.
[0077] A timing hole (see
[0078] In addition, the media-transport belt 108 should be totally opaque, so as to not interfere with a belt speed sensing device located beneath a timing hole (T.H.), and be able to sense through an edge margin of belt 108 (
[0079] Perforating the Seamed Transport Media in a Predefined Pattern
[0080] The seamed transport media, such as in the configuration of a belt, can be perforated, that is apertures or holes formed therein entirely through the belt in a predetermined pattern by, for example, EM/Belting Industries, resulting in a belt 108 shown, for example, in
[0081] Specific embodiments will now be described in detail. These examples are intended to be illustrative, and are not limited to the materials, conditions, or process parameters set forth in these embodiments.
Example I
[0082] There was prepared a seamed vacuum transport media belt as follows:
[0083] Two carboys or containers are filled with a total of 28 pounds (lbs.) of stainless steel shot and EMPEROR 1200, BYK 333, diethyl phthalate, and methylene chloride as illustrated in the following table, followed by mixing/milling for eight hours. The resulting two container contents were merged to form the mill base, which was then added to pressure pot and let down with a 10 VITEL 1200B/methylene chloride solution, resulting in the final coating composition of EMPEROR 1200/VITEL1200B/BYK333/diethyl phthalate with a ratio of 47.4/47.4/0.5/4.7 in methylene chloride, about 11.94 percent solids.
TABLE-US-00001 TABLE COMPONENT MASS (LB.) EMPEROR 1200 (conductive carbon black) 3.65 VITEL 1200B (polyester copolymer) 3.65 Methylene Chloride (solvent) 56.49 Diethyl Phthalate (plasticizer) 0.37 BYK 333 (leveling agent) 0.037
[0084] The above prepared coating dispersion was then coated, via extrusion, onto a 4 mil thick bio-based generated polyethylene furan-2,5-dicarboxylate substrate layer (PEF), and then subsequently dried at 266 F. for 3 to 4 minutes. The coating resulting was about 10 to about 15 microns in thickness as can be determined by a Permascope and possesses a surface resistivity of about 1.010.sup.4 /square as measured with a known Trek Model 152-1 Resistance Meter.
[0085] The above prepared belt sheet, while in roll form, was ultrasonically welded into a belt/loop that measures about 655 millimeters in diameter and was about 440 millimeters wide. The welding process was accomplished with Branson ultrasonic welding equipment to continuously join the overlapped seam. The process parameters were designed to remove any coating in the overlap areas to facilitate the joining of the two ends of the belt sheet together such that the seam break strength as measured by Instron Universal Tester was greater than about 50 lbs/in. The material that is squeezed out the ends of the seam was removed, and a timing hole was added.
[0086] Alternatively, the aforementioned steps can be combined with a high tolerance material slitting of the media transport sheet, and an edge offset reduction vision system can be used during the overlap process so that the loop's edge do not vary by more than about 300 m throughout its circumference, resulting in an active steering system to produce a highly accurate motion/location registration of the transport belt.
[0087] The prepared seamed belt was then perforated in a predefined pattern by OEM/Belting Industries, see for example,
[0088] It is believed that ink jet machine laboratory testing at ambient conditions will show a decrease in static field voltage on the coated surface of the belt from an average of about 250 volts to about 25 volts, no noticeable misting of printhead faceplates after about 5,000 cycles at about 50 F. and 20 percent relative humidity, and the absence of droplets returning to contaminate the inkjet faceplates.
[0089] The claims, as originally presented and as they may be amended, encompass variations, alternatives, modifications, improvements, equivalents, and substantial equivalents of the embodiments and teachings disclosed herein, including those that are presently unforeseen or, unappreciated, and that, for example, may arise from applicants/patentees and others. Unless specifically recited in a claim, steps or, components of claims should not be implied or, imported from the specification or, any other claims as to any particular order, number, position, size, shape, angle, color, or, material.