The present invention relates to the manufacturing of steel Yankee driers.
Steel Yankee driers are known to have been put on the market relatively recently. In the past, the Yankee driers were made of cast iron.
It is known that steel Yankee driers can be manufactured according to several manufacturing techniques. The most frequent embodiments are the following:
The use of steel provides many advantages:
Further advantages are generally associated with a higher operative flexibility of steel Yankee drier compared to cast iron Yankee driers. In fact, in case of cast iron Yankee driers, a model was required for each size of Yankee drier to be manufactured in the foundry. The manufacturing process rigidity did not allow the manufacturer to easily adapt the Yankee drier geometry to the variable needs of the market.
However, cast iron is more resistant to corrosion compared to steel.
The internal surface of the Yankee drier is always in contact with steam and condensate produced by the heat exchange with the paper to be dried on the external surface of the Yankee drier. The quality of the steam introduced into the Yankee drier must be constantly controlled to avoid corrosion inside the Yankee drier and the components of the steam generation and recirculation units (boiler, thermo-compressor, pipes etc.) arranged external to the Yankee drier. Maintaining the required chemical and physical properties of the steam and the condensate, and the absolute absence of oxygen and corrosive substances in the circuits avoid progressive corrosion both in the cast iron and the steel Yankee driers. However, it is noted that steel Yankee driers are more subject to corrosion compared to cast iron Yankee driers in case of deviation from the parameters suggested by the manufacturer. In case of presence, even limited, of oxygen in the steam or acidity exceeding the limits suggested by the manufacturer, steel tends more easily to form layers of unstable oxide that are subject to detachment. This has a double negative effect: over the time, if a correction is not actuated, there is distributed or localized reduction of the thickness of the steel with possible damages to the Yankee drier; moreover, in a relative short time the oxide, once detached, tends to obstruct the condensate collecting tubes. When the condensate collecting tubes are obstructed, the mechanism for extracting the condensate does not work as desired and there is an increase in the fluid dynamic pressure drops and the formation of areas where the heat exchange with the external surface is reduced. A negative effect is that the paper exhibits wet bands due to a non-correct drying thereof.
Such problems can normally be managed by correcting the quality of the steam through chemical analysis of the condensates and use of chemicals for the correction of off-scale parameters. This correction can be facilitated by automatic chemical analysis systems connected to automated chemicals dispensers.
In some cases, however, this correction is difficult to manage. This occurs mainly in two cases:
Especially in the second case, since the steam is not specifically produced for use in Yankee driers, the deviation from the correct quality parameters is frequent. Moreover, the paper mill cannot control such parameters to limit their corrosive effect on the internal surface of the Yankee drier. In addition, the lack of control on the steam production process makes it possible to receive steam containing corrosive substances, possibly used during maintenance or washing of the plants located upstream of the paper mill.
The main object of the present invention is to overcome the above-mentioned drawbacks.
This result is achieved, according to the present invention, by providing a steel Yankee drier having a protective coating on its internal surface, in particular the internal surface through which the most part of the heat exchange with the paper and the steam condensation takes place. Such a Yankee drier has the following characteristics:
In order to limit the increase in thermal resistance to the transfer of heat towards the paper, the protective coating has a relatively reduced thickness. In particular, the coating thickness I less than 200 micron. Preferably, the coating thickness is less than 100 micron. Optimal values for the coating thickness, especially on the condensate formation surfaces, are not higher than 50 micron.
The thermal resistance of the heat transfer coated surface is not higher than 10% compared to the same surface non provided with the protective coating. Preferably, said thermal resistance increase is not higher than 2%.
The protective coating must have a high surface hardness so as to adequately resist to the possible erosive effect caused by oxidized particles generated either inside the Yankee drier or from parts external to the Yankee drier (for example generated in the steam circuits)—The steam and the condensate exiting the Yankee drier would drag such particles. At the points where the condensate is extracted, the speed of dragging can reach high values due to the reduced passages; the erosive effect deriving from the contact of the entrained particles with the coated surface could have the effect of removing or locally eroding the coating if the latter does not exhibit an adequate hardness. In particular, the hardness of the protective coating, measured at room temperature (25° C.), is higher than 400 HV. Preferably, the hardness of the protective coating at room temperature is higher than 400 HV. Optimal values for the hardness of the protective coating at room temperature are higher than 550 HV.
The protective coating covers at least the surfaces where the condensate is collected. Preferably, the protective coating is applied over the entire surface through which transfer of heat towards the paper takes place.
These and further advantages and characteristics of the present invention will be more and better understood by the skilled in the art thanks to the following description and the attached drawings, provided by way of example but not to be considered in a limiting sense, in which:
The Yankee drier shown in
The steam passes from the tubular inner chamber (3) to the annular external chamber (4), delimited by the internal surface (1) of the mantle (15) and the external surface of the tie rod (12), through holes (5) provided on the surface of the latter.
In operation, the paper (7) adheres to the external surface (11) of the mantle (15). The paper covers the most part of the mantle surface along the width of the latter, leaving uncovered only the connection areas between the end heads (13, 14) and the mantle (15). The part of the steel mantle comprised between the internal surface (1) and the paper (7) is the part through which takes place the most part of thermal exchange originating from the heat introduced through the steam. The heat transmission causes the steam to condensate. The condensate (C), due to centrifugal force, tends to accumulate on the radially outermost parts of the internal surface (1) of the mantle (15).
Typically, the Yankee driers have circumferential grooves (8) formed on the internal surface of the mantle (15). Said grooves have a dual function: to increase the heat exchange surface increasing the thermal efficiency of the system and collecting the condensate that concentrates on the bottom of the same grooves. The condensate extraction system (not shown) is typically composed of a series of tubes placed with their respective ends at a predetermined distance from the bottom of the grooves (8). The steam is generally introduced in a larger amount in relation to the amount strictly required, such that not all the steam is subjected to condensation and a certain amount of steam is used as a carrier for removal of the condensate. Therefore, through the tubes of the condensate extraction system is removed thanks to the excess of steam.
In
The present invention also applies to Yankee driers made in a different way like, for example, Yankee driers made as shown in
A further configuration is shown in
In the drawings, the protective coating (9) is generally represented by a thicker line.
The following description provides a possible way of applying the protective coating and involves the so-called high phosphorus nickel plating. Compared to other techniques for forming protective coatings on metal bodies, it provides the following advantages:
Nickel plating is an auto-catalytic process allowing the deposition of a Nickel-Phosphorus alloy layer on a metal substrate.
The nickel is used in solution in solution in the form of salts thereof (NiSO4) and then precipitates thanks to its chemical reduction. The reducing agent is identifiable in the hypophosphite ion (H2PO2) present in the nickel bath as sodium hypophosphite (NaH2PO2). The speed at which the alloy is deposited and the phosphorus content depend on the amount of phosphite and hypophosphite in the nickel bath.
The process described above is represented by the flowing equation:
H2PO2+Ni2—H2O-->Ni+2H+H2PO3−
The thickness of the Ni—P alloy deposited according to this technique is very uniform on all points of the surface to be coated and depends on the time of contact with the bath. By this process it is generally possible to treat pieces having a relatively complex geometry, realizing a protective coating having a uniform thickness over the entire surface of the treated pieces. A further advantage of the nickel plating is that the protective coating is sufficiently hard and resistant to corrosion in relation to its application to the manufacturing of Yankee driers.
The metallurgical properties of the deposited protective coating are function of the phosphorous content. According to the phosphorous content three categories can be defined:
A high phosphorous content alloys is preferred for realizing a protective coating by chemical nickel plating in accordance with the present invention: such a protective coating will exhibit, in fact, higher corrosion resistance and ductility that are suitable for this specific application.
Typically, chemical nickel coating is implemented by immersing the component to be coated in a chemical bath having a given chemical composition, at a predetermined temperature and a given degree of turbulence.
In accordance with the present invention, there is a need to coat only the internal surface of the Yankee drier. Yankee driers are extremely larger than components normally subjected to chemical nickel plating. To this end, it is useful to consider that the most compact Yankee driers have a minimum diameter of 2-3 m and a width of 3 m; larger Yankee driers can have a diameter exceeding 6-7 m and a width higher than 6 m. Since Yankee driers are pressure vessels subjected to fatiguing stress, the thickness of the structural parts is high, therefore their weight can easily exceed tens of tons (the bigger Yankee drier can have a weight of more than 150 tons). Nickel plating by immersion of objects having such a size would be a very complex operation because it would require the immersion of the Yankee drier, or at least the mantle, in a enormous tank completely filled with a nickel bath. Such an approach would involve a number of drawbacks that would reduce its convenience. In fact, the tank would have to be of such dimension to contain the Yankee drier, special supports for supporting the Yankee drier inside the Yankee drier would be required, and a large amount of nickel bath would be required for at completely covering the Yankee drier or partially covering the latter providing means for ensuring the contact of the bath with all surfaces to be coated.
The purpose of the protective coating according to the present invention is the protection of internal surfaces of the Yankee drier, i.e. surfaces coming into contact with steam and forming condensate, while the coating of other surfaces of the Yankee drier, where the absence of condensate eliminates the risk of oxidation and corrosion, is not required.
The complete immersion of the Yankee drier in the nickel bath, as normally occurs for smaller components, would inevitably lead to the coating of all surfaces in contact with the bath, including those surfaces for which a protective coating is not required. In the context of the present invention, this would imply unnecessary additional costs since the formation of protective coating implies consumption of nickel and phosphorus contained in the nickel bath. In addition, some of the surfaces coated by the protective coating following a total immersion of the Yankee drier in the nickel bath should be brought back to their non-coated state. This further process step would concern, in particular, the external surfaces of the Yankee drier that must be metallized and, in particular, the surfaces that delimit welds to be made in the subsequent manufacturing step. For example, if the mantle is immersed in the nickel bath before connecting the end heads to the mantle and a welded connection between these parts is required, the surfaces provided for the subsequent welds should be further machined to eliminate the nickel-phosphorus coating, due to the presence of phosphorus that, once dissolved in the welding substances normally used, would cause unacceptable welding defects and impurities. In addition, the chemical reaction producing the formation of the protective coating requires heating of the nickel bath at a given minimum temperature. Indicatively, the reaction activates when the nickel bath temperature is above 60° C. A large amount of nickel bath would require heating means capable of transmitting large quantities of heat, with large energy loss, in order to reach the required temperature in a reasonable time. Moreover, a large tank for immersing the mantle in the nickel bath would have large containment surfaces and, therefore, would imply large thermal losses and additional heat for maintaining the required temperature over the time needed for completing the coating process.
Thus, in summary, the technique normally adopted in industrial chemical nickel-plating processes would imply great technological/engineering difficulties to obtain the coating of a large component like a Yankee drier. Furthermore, excessive amounts of nickel and phosphorus would be used for coating surfaces that do not require coating. Further economic inefficiencies would derive from the thermal energy required to heat an unnecessarily large nickel bath.
The example described below provides a method for using a chemical nickel-plating technique optimized for the internal surfaces of a Yankee drier.
The concept on which the following example is based is that the protective coating is not provided by immersing a Yankee drier in a nickel bath but it is provided by using the internal surface of the Yankee drier as a container for the nickel bath.
According to the preferred embodiment of a method for forming a protective coating as shown in
Once the caps (12, 13) are mounted, the nickel bath can be introduced in the mantle.
The nickel bath is composed of a mixture of nickel salts and sodium hypophosphite. The nickel bath may also comprise:
The nickel bath (24) will not completely fill the volume inside the cylindrical mantle
The amount of nickel bath initially introduced in the mantle and laterally contained by caps (12) and (13) is such that the upper level (23) of the nickel bath is preferably above the chord (29) of the lowermost sector (in the drawing, the sector 19), formed on the circumference (27) defined by the bottoms of grooves (8) formed in the mantle. The level (23) can also preferably be above the chord (30) of sector (19) formed on the circumference (26) defined by the radially innermost part of the grooves (8). In this way, when the mantle will be rotated to expose another sector (for example, sector 20) to the nickel bath, there will be a superimposition of the protective coating formed in the first step to the protective coating formed in the subsequent step. Therefore, it will be possible to completely coat the internal surface of the mantle that will be in contact with the condensate when the Yankee drier will be in operation.
The preferably circular openings (17, 18) formed in the caps (12, 13) are such that they always remain above the level (23) of the nickel bath, even after a complete rotation of the mantle around its longitudinal axis.
Once introduced in the mantle, the nickel bath must be brought to a temperature suitable for the desired deposition (typically, a temperature comprised between 60° C. and 95° C.). During this phase, the mantle is stationary. For heating the nickel bath, it is possible to make use of both heating means placed externally to the mantle and heating means immersed in the nickel bath. For example, it is possible to make use of radiant lamps placed externally around the mantle so as to selectively or simultaneously heating the sectors mentioned above. In this case, the lamps can be uniformly distributed to uniform the temperature of the outer surface of the mantle subjected to heating and avoid areas that are heated more than others. Alternatively, or in addition, it is possible to make use of heating means totally or partially immersed in the nickel bath. For example, immersed electric heating resistors can be used.
To speed up the activation of the chemical deposition process, the nickel bath can be pre-heated before introducing it into the mantle.
Preferably, the nickel bath is recirculated inside the mantle for two reasons: a limited turbulence of the nickel bath facilitates removal of hydrogen micro-bubbles that tend to adhere to the treated surface. A second reason is that the content of nickel, phosphorus and other substances contained in the bath progressively decrease while the reaction takes place and the protective coating is formed. If the nickel bath is not mixed, some parts of the latter could have a non-uniform concentration due, for example, to a (even if limited) an uneven distribution of the temperature.
The mixing and turbulence in the nickel bath can be obtained in different ways. A preferred embodiment, schematically represented in
Another embodiment can foresee a heater (33) placed at any point of the recirculation system, preferably downstream of the filter (preferably an electrical heating resistor). This heater can cooperate with, or substitute the, heating system for heating the nickel bath disclosed above.
A cover (36) can be placed above the nickel bath, preferably not rigidly connected with the mantle so as to allow the latter to rotate without having to reposition the cover (36) at each rotation of the mantle. The purpose of said cover is to hinder the dispersion of vapors produced by the reaction: the nickel bath, even if not brought to the boiling point, can be brought o relatively high temperatures (preferably up to 95° C.) such that a high evaporation is expected, due also to recirculation and turbulence mentioned above. The presence of a cover allows the condensation of part of the vapors and its re-introduction (for example, by dripping) into the nickel bath. In this way, at least two advantages are obtained: the nickel bath consumption is reduced such that reintegration of demineralized water in the nickel bath is also reduced, and thermal losses are limited, thus reducing the thermal power required for reaching the desired temperature and its control during the process.
Preferably, said cover is as large as possible to increase its efficiency. Ideally, the maximum efficiency is achieved by completely covering the nickel bath.
As said above, the cover (36) is preferably stationary also during rotation of the mantle. Therefore, preferably, the cover is supported by a structure constrained to a part external to the mantle, for example supported by abeam (37) passing through the openings (17, 18) of the caps (12, 13) and supported by columns (38, 39) bearing on the ground externally to the mantle. The cover can be connected to the beam (37) by means of cables or tie rods (40).
Preferably, said cover is made of a thermally insulating material or it is coated with a thermally insulating material. Preferably, said cover can be provided with coverable openings allowing visual inspection of the nickel bath or collection of samples to be analyzed.
Once the nickel bath has been brought to a temperature higher than the reaction triggering temperature, the Ni—P coating deposits on the treated surfaces. The deposition rate will also depend on the temperature of the nickel bath (a higher temperature will imply a higher deposition rate).
Preferably, the mantle is kept stationary for a time sufficient to allow the deposition of the protective coating having the desired thickness. During the reaction process, it will be possible to manually or automatically add substances containing nickel and/or phosphorus to avoid excessive variations of the nickel bath composition with respect to the starting composition, variations due to the progressive deposition of nickel and phosphorus. Other substances can be added to the nickel bath (for example, pH regulators) in order to keep the acidity of the solution within the limits required for the reaction.
Once the surface of the mantle corresponding to the first of the above-mentioned sectors has been exposed to the reaction for the predetermined time required for the deposition of the protective coating having the desired thickness, the mantle is rotated about its longitudinal axis through rollers (10) and (11). The rotation of the mantle, indicated by the arrow “R” in
As said above, the level (23) of the nickel bath is such that, preferably, there is an overlapping of the protective coating at the ends of the surfaces exposed to the nickel bath in order to avoid uncoated areas in the mantle inner surface to be coated.
Preferably, the surface of the mantle corresponding to the sector (20) is pre-heated before being brought into contact with the nickel bath, the pre-heating bringing said surface at a temperature lower than, or equal to, the temperature of the nickel bath such that, when there is the contact of the surface with the nickel bath, the temperature of the latter is not excessively or quickly reduced given the high thermal conductivity of the mantle. An excessive or too quick decreasing of the bath temperature (indicatively, a temperature decrease of 10° C. occurring during said rotation) could slow down or interrupt the reaction providing the deposition of the protective coating that, as a consequence, could be defective or it could have a thickness lower than the desired thickness.
The step disclosed above is repeated as many times as the number of sector subdivisions. Therefore, at the end of the process, the entire internal surface of the mantle exposed to the nickel bath will be coated by a protective coating having a substantially uniform thickness with the exception of said overlapping zones where the protective coating will have a higher thickness. According the example disclosed above, said operation is executed four times, i.e. for each of said sectors (19, 20, 21, 22).
In some other embodiments, the mantle can be attached to the end heads (13, 14), as shown in
According to an alternative implementation of the process, the mantle can be rotated about its axis also during the reaction, i.e. during the deposition of the protective coating. In this way, overlapping zones of protective coating are avoided. In this case, the protective coating is formed by superimposed layers formed along the internal cylindrical surface of the mantle. The number of the superimposed layers will be equal to the number of complete rotations of the mantle.
In practice the execution details may vary with regard to the elements described and illustrated, without thereby departing from the adopted solution and therefore remaining within the limits of the protection granted by this patent in accordance with the appended claims.
Number | Date | Country | Kind |
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102019000004363 | Mar 2019 | IT | national |
Filing Document | Filing Date | Country | Kind |
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PCT/IT2020/050069 | 3/23/2020 | WO | 00 |