FIELD OF THE INVENTION
- Top of Page
This invention relates to a method for manufacturing gravure printing cylinders.
- Top of Page
OF THE INVENTION
The plating of copper from acid solutions is well known, with numerous industrial applications. In most applications the articles to be plated are suspended in the electrolyte, a technique generally referred to as rack plating. Rack plating is a well-known process and examples of the process may be found in U.S. Pat. No. 3,939,056 to Fueki et al., U.S. Pat. No. 4,176,039 to Wismer, and U.S. Pat. No. 4,297,197 to Salman, the subject matter of each of which is herein incorporated by reference in its entirety.
Another application well known to those in the industry is copper plating steel and aluminium cylinders used for printing applications, such as gravure printing, wherein steel or aluminium is used to provide a cheap and sturdy substrate for the engraveable copper coating. Gravure printing is a method using the Intaglio process in which the image to be printed consists of depressions etched or engraved usually to different depths. Slightly viscous solvent inks are applied to the entire surface and a metal doctor blade removes the excess ink from the non-printing surface. Normally engraving is performed on a copper plated cylinder, which is subsequently chrome plated to minimize wear.
The electroplating and other associated treatment of the printing cylinders normally takes place in a suitable tank containing an electrolyte into which the cylinder is partially or wholly immersed. The cylinder is made the cathode and a direct electric current is passed through the cylinder and electrolyte with suitable anodes completing the circuit with a power supply. The cylinder is rotated during the process and the tanks are normally fitted with filtration and temperature control equipment to provide good process control. If desired, further solution agitation equipment such as air or solution movement may be utilized.
Printing cylinders are prepared for acid copper plating by first cleaning the surface to remove oils, dirt and grease and surface oxidation products, thereby providing a suitable surface for electroplating. Steel cylinders are then coated in a thin layer of copper from a solution of copper (I) ions, normally from a cyanide-based electrolyte. This ensures an adherent copper deposit by avoiding the displacement reaction experienced with copper (II) electrolytes on steel substrates that may lead to poorly adherent deposits. Aluminium cylinders are processed through a chemical pre-treatment that produces a thin zinc layer on the aluminium, which then renders the substrate suitable for applying a thin layer of copper or nickel from solutions of near neutral pH.
The cylinders with a thin copper or nickel deposit are then copper plated from an acidic copper (II) electrolyte to build up a thick layer of copper, normally in the order of 100 to 500 microns. Acidic copper electrolytes are preferred to copper (I) electrolytes for the second stage because of their ability to plate faster by the use of high current densities. Typically current densities of 20 to 25 A/dm2 are employed. Examples of prior art processes for copper plating of gravure printing cylinders are described in U.S. Pat. Nos. 5,417,841 and 4,781,801 to Frisby, the subject matter of each of which is herein incorporated by reference in its entirety.
Due to the nature of the current distribution during the plating process, the copper deposit on the printing cylinder can be very uneven and the ends of the cylinders generally tend to have a much thicker deposit than the center of the cylinder. The degree of this variation varies according to the cylinder dimensions and the plating conditions, but it is not uncommon for a printing cylinder to have a copper deposit where the thickness at the cylinder ends is twice the thickness as the center of the cylinder, which makes the cylinder unsuitable for the printing process. To make the cylinder suitable for printing, the copper plated cylinder must be treated to provide a surface that has a deposit, for example, that does not vary more than about +/−2 microns across the cylinder surface. This is normally achieved by two polishing operations; first, a machining operation that removes relatively large amounts of copper, and secondly a fine polishing operation.
Cylinders that have been electroplated, machined and polished as described above are then ready to be engraved or etched with the design to be printed. For accurate and consistent engraving it is necessary that the copper deposit be of a suitable uniform hardness, which can be controlled by additives in the copper plating solution. It is also necessary that the copper deposit is free from deposit imperfections such as voids (pits) and roughness. Once engraved or etched with the print design, the cylinders are electroplated with a thin layer of chromium to provide wear resistance during the printing operation.
During the printing operation, wear of the cylinder takes place and worn cylinders are typically reconditioned by removing a predetermined thickness of deposit by a further machining stage, such that the entire print design is removed from the cylinder surface. The thickness removed is normally in the order of about 100 microns. The cylinder can then be made suitable for further electroplating of copper to return the deposit to the original plated thickness. Subsequently, the cylinder is subjected to the normal machining, polishing and engraving process and made useable for further printing. In this way a single cylinder can be used continually.
The drawback of the current technique for preparing cylinders is that in order to achieve the desired thickness across the entire length of the printing cylinder, a minimum thickness of copper must be deposited in the center of the cylinder. The excess is then removed from the edges by machining, which is a costly and time-consuming operation that generates a large amount of waste copper metal. Thus, there remains a need in the art for an improved process for preparing gravure printing cylinders that does not require a subsequent machining step to achieve an even deposit of copper across the length of the printing cylinder.
The use of pulse reverse plating techniques to deposit copper from acidic solutions is well-known within the electronics industry, for plating copper from acidic solutions onto printed circuit boards and other substrates. U.S. Pat. No. 6,319,384, to Taylor et al., the subject matter of which is herein incorporated by reference in its entirely, discloses a method for the electrodeposition of copper onto a semiconductor substrate, wherein the acidic copper plating bath is substantially devoid of brighteners and and/or levellers.
The basic chemistry of the additives used for electronics applications, and their performance under pulse current plating conditions as compared to direct current conditions is explained by T. Pearson, “Effect of Pulsed Current On The Electrodeposition of Chromium and Copper”, PhD thesis, Aston University, United Kingdom, 1989. The additives are broadly similar to those used in general rack plating applications, and broadly comprise a sulfopropyl sulfide and a polyalkylene glycol that operate in conjunction with chloride ion. These holes are typically 0.5 mm diameter and 2-3 mm deep. Typically the cathodic current density used in the plating of printed circuit boards is in the order of 2.0 A/dm2, but due to the geometrical factors the effective current density in the holes is extremely low and much lower than the average current density applied to the board as a whole.
U.S. Patent application publication No. 2004/0074775 to Herdman et al., the subject matter of which is herein incorporated by reference in its entirety, describes the use of pulse reverse plating and acid copper electrolytes for decorative copper applications such as plating on plastics for automobile or sanitary applications, or plating on alloy automobile wheels. The process provides for improved distribution of the copper deposit across the substrate. The current density range described in the above application is 0.5-5.0 A/dm2 but typically the applied current density is 2.0-3.0 A/dm2. However, this current density range is about an order of magnitude below the current densities require for the copper plating of printing cylinders.
A further recent U.S. Patent application publication No. 2002/0079228 to Smith, the subject matter of which is herein incorporated by reference in its entirety, describes an apparatus and method for electroplating of gravure printing cylinders. The method employs the application of pulse reverse plating to a bath based upon copper sulfate, sulfuric acid and chloride ion.
The inventors have surprisingly found that the pulse reverse current plating techniques used for printed circuit boards can also translate very well to the application of plating copper in the conditions used for plating printing cylinders. This is surprising in that the current density range is very different from that applied during plating of printed circuit boards or during rack plating applications, and also surprising because in normal electroplating applications an increased current density results in a worse metal distribution. When printing cylinders are plated using pulse reverse plating in conjunction with an additive system optimized for pulse reverse electrolysis, the distribution of copper deposit across the length of the cylinder is dramatically improved. This has two distinct advantages to the plater: (1) a reduction in excess copper deposited on the ends of the cylinder, and (2) the central area of the cylinder can be plated to the required thickness in a reduced time or at a reduced current density. The advantages described above can lead to reduced polishing requirements, reduced scrap metal production, increased production capacity and energy savings. The deposits produced are levelled, free from surface imperfections and hardness control can still be achieved by certain bath additives.
- Top of Page
OF THE INVENTION
The use of pulse reverse plating to deposit copper can be used for a method of plating printing cylinders in an acidic copper electroplating bath comprising the steps of:
(a) suspending the cylinder in a plating bath comprising copper ions, counter ions, chloride ions, a polyalkyleneglycol and a bath-soluble divalent sulfur compound; and
(b) plating the cylinder for a sufficient period of time with alternating cathodic and anodic current to produce a desired thickness of copper on the surface of said cylinder.
- Top of Page
OF THE INVENTION
The present invention utilizes pulse-reverse current for plating gravure printing cylinders with copper in an acidic copper plating bath to produce a desired thickness of copper on the surfaces of the cylinders. The present invention is particularly useful for plating a uniform thickness of copper across the length of the printing cylinder.
The acidic copper plating bath of the invention generally comprises copper ions, a source of counter ions, chloride ions, a polyalkylene glycol, and a bath-soluble divalent sulfur compound. Other additives such as wetting agents may also be added to the bath to improve the copper deposit.
Copper ions are present in the plating bath at a concentration of about 30 to 70 g/l. Copper sulfate pentahydrate is an example of a copper compound that is useful in the baths of the present invention. Other copper compounds known to those skilled in the art, including as copper methanesulfonate, and mixtures of such compounds, are also suitable. The plating bath generally comprises the copper sulfate pentahydrate at a concentration of about 120 to 280 g/l, preferably about 150-200 g/l.
The source of counter ions in the plating bath is most commonly sulfate ions, but may also be methanesulfonate ions or a mixture of such ions. A preferred source of sulfate ions is sulfuric acid. Where sulfate is the counter ion, sulfuric acid is normally present in the plating bath at a concentration of about 50-250 g/l, preferably about 80-140 g/l, and most preferably about 100-110 g/l.
Chloride ions may also be present in the plating bath, at a concentration of about 10-500 mg/l, preferably about 75-150 mg/l. The source of chloride ions in the plating bath is preferably hydrochloric acid.
The polyalkyleneglycol is generally present in the plating bath at a concentration of between about 50 and 10,000 mg/l, preferably between about 300 and 1,000 mg/l. The polyalkyleneglycol typically has a molecular weight of between 500 and 100,000. Preferred polyalkyleneglycols include polyethylene glycol and an ethylene oxide/propylene oxide co-polymers. A mixture of such suitable polyalkyleneglycols may also be used.
The bath-soluble divalent sulfur compound is generally present in the plating bath at a concentration of about 1-150 mg/l, preferably about 30-50 mg/l. Preferred divalent sulfur compounds include, but are not limited to, mercaptopropanesulfonic acid or an alkali metal salt thereof, bis-(propane-3-sulfonic acid) disulfide or an alkali metal salt thereof, and bis-(ethane-2-sulfuric acid) disulfide or an alkali metal salt thereof, and mixtures of one or more of the foregoing.