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(11) | EP 0 572 941 A1 |
| (12) | EUROPEAN PATENT APPLICATION |
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| (54) | Apparatus and method for the electrophoretic painting of metal structures, in particular of metal sheet coils |
| (57) The present invention concerns an apparatus and the relative process for the electrophoretic
painting of metal structures (29), in particular for the electrophoretic painting
of metal sheet coils. The counter-electrodes (3,20) dipped into the electrophoretic bath have a main element (21) (for instance a plate) on which holes (22) are provided, associated with groups of points (23). With the new counter-electrodes an uniform electric field is obtained on the entire coil surface, thus obtaining a constant thickness of the protective coat (ca. 3 µm). |
FIELD OF THE INVENTION
[0001] The present invention concerns a new apparatus and a new process for the electrophoretic anti-corrosion coating of metal sheet coils. The protective coat makes it possible to stamp the metal sheets without using lubricating oils, to electrically weld them, and it can, because of its composition, be removed by means of alcaline degreasing agents.
[0002] It is very important to have a coat of uniform thickness over the entire width of the coil. The optimum thickness of the paint coat was found to be 3 µm, plus or minus 0.5 µm. In fact the possibility of welding the sheets depends on the thickness of the protective coat, which, acting as an insulation, presents to the passage of an electric current a resistance which is directly proportional to the thickness of the protective coat. Ordinarily, a thickness higher than 3.5 µm requires voltages unacceptable for point welding, producing large amounts of fumes and carbon residues which reduce to a considerable extent the life of counter-electrodes.
[0003] On the other hand, a thickness lower than 2.5 µm, even if favourable in as far as the welding is concerned, does not allow, during the stamping of the sheets, to obtain the necessary lubrication, because it fails to cover the "points" coming out of the sheet surface.
[0004] Because of this, and of the high pressure exerted by the stamping press, seizure of the stamp on the sheet and breaking of the sheet take place.
PRIOR ART
[0005] The machinery mostly employed up to now for applying layers of a protective coating on coils consists essentially of rollers covered with the paint to be applied. In this way, it is possible to apply coatings of a required thickness, which however, is not constant throughout the sheet.
[0006] The difficulty of obtaining coats of strictly constant thickness increases with an increase of the band width, and for the often employed widths of 180 to 200 cm it becomes practically impossible.
[0007] This difficulty derives from the fact that the metal bands are not perfectly even, but show slight undulations, which produce concavities on one face corresponding to convexities on the opposite face.
[0008] As the protective paint has to be applied to both faces, in the roller application system, while one face of the metal band turns on a guiding steel roller, the other face is pressed by the roller applying the protective coat.
[0009] As a result of the opposite forces exerted on the band, the band itself, when the protective film is applied on the first face, is in most cases flat, and the thickness of the protective film results within the tolerance limits. On the other hand, when the protective coating application on the opposite face takes place with the aid of a similar roller, no counter-roller can be pressed on the freshly painted surface in order to make the sheet perfectly plane.
[0010] Therefore the thickness of the protective paint film on at least one face of the coil is not constant throughout; this is the cause of the problems which arise in the welding and stamping, as said.
[0011] In order to improve the welding of the sheets, the use of electricity conductor pigments and mineral charges was suggested.
[0012] These particles improve in fact the welding; however, during the stamping, these substances, in the form of microscopic powders, collect on the counter-stamp and coagulate, producing, because of the high pressure exerted, very serious damages to the stamps, with ensuing economic losses for the plant owner. For this reason, the use of substances of this type is avoided.
SUMMARY OF THE INVENTION
[0013] With the aid of the apparatus, which is an object of the present invention, the deposition of protective films of the special paint, having a rigorously constant thickness (optimum value: 3 µm), with very limited departures (± 0.5 µm) from the nominal value, may be obtained.
[0014] The electrodes employed in an apparatus of this type may advantageously be used for both anodic and cathodic electrophoresis.
[0015] The basic component of an electrophoretic paint is the binder, in practice a polymer or a resin. The resin may be of various types (alkyd, epoxy, acrylic, polybutadiene, poliesther, etc.) depending on the mechanical, physical and chemical characteristics to be obtained. For instance, an acrylic resin shows a good light resistance, while an epoxy resin resists to corrosion. As said, in the case of coils epoxy resins are commonly employed to protect them from corrosion.
[0016] In paints for anaphoresis, the resin will be of RCOOH type, while in cathaphoresis it will be of R₃N type, R being a radical which may contain alkyd, epoxy, acryl, etc., groups.
[0017] In order to make these resins soluble in water, it is necessary to add a neutralising or solubilizing agent which forms soluble salts with resin; bases (in general ammines) are added to the anodic resins, whereas acids are employed for the cathodic ones.
[0018] Thus the following reactions take place:
anodic resins
RCOOH + YOH water = RCOO⁻ + Y⁺ +H₂O
(or RCOOH + R₃N = RCOO⁻ + NR₃H⁺)
cathodic resins
R₃N + HX water = R₃NH⁺ + X⁻ water
Further paint ingredients are reticulating agents, pigments, solvents and additives, which are added to the resin prior to its solubilization in water.
[0019] Reticulants normally consist of ammine resins or blocked isocyanates and are added in order to polymerize the paint ingredients.
[0020] Pigments are added to impart colour and covering power to the paint or to improve in general its characteristics.
[0021] Solvents give stability to the system and improve all the film characteristics. Additives improve and exalt all the film characteristics.
[0022] Electrolysis of water is one of the most important processes for the formation of a paint film.
[0023] It takes place in water containing ions due to the dissociation of alkalies, acids or salts; the amount of the electrolysis products depends on the density of the current passing through the bath and on time.
[0024] For convenience, we will consider anaphoresis; however, similar phenomena take place also in cathaphoresis.
[0025] The resins are charged negatively and are solubilized by positive charge bearing alkalies; under the action of the electric field, the acid parts (resin and any other acidic material) migrate to the anode at the rate 1-4 µm/sec.v., while the alcaline parts migrate to the cathode in an amount equivalent to a rate of 2-7 µm/sec.v.
[0026] At the anode following reactions take place:
2H₂O ⇄ 4H⁺ + O₂ ↑ + 4 e⁻(acid is developed; oxidation)
The acidity (H⁺) developed in this reaction lowers the pH to 2.5-3.5 in a zone distant 25-30 µm from the metal, causing the rapid coagulation of the paint product which is soluble only at a pH higher than 6-8, according to the reaction:
RCOO⁻ + H⁺ → RCOOH (film deposition)
At the cathode the basic neutralizing agent will be discharged, which returns immediately in the bath.
[0027] In substance, only water electrolysis takes place:
2H₂O + 2 e⁻ ⇄ H₂ ↑ 2 O H⁻ (alkali development)
The neutralizing agent will be eliminated at the cathode only if it is gaseous and scarcely water soluble, or in case dialysis cells are employed which take it up from the bath.
[0028] At the anode the following phenomena take place:
- concentration of the paint product and of the acids which lose their electric charge, and rarefaction of the alkalies;
- lowering of the pH;
- development of O₂
- rarefaction of the paint product and concentration of the alkalies, which adsorb electric charges corresponding to the ones listed at the anode;
- increase of the pH;
- development of H₂.
[0029] In anode electrophoresis the protective paint may consist, as a non limiting example, of an acrylic thermoplastic carboxylated resin made water soluble by salification with bases such as ammonium hydroxide and/or amines, and of a dispersion of a wax having particular characteristics of hardness, melting point and average particle dimensions.
[0030] The paint maintains, after the application and drying (at 180°c), a thermoplastic structure such as to be easily removed by an alkaline wash.
[0031] The dried paint film has a friction coefficient of between 0.04 and 0.08 which allows the forming of the sheet without breakage of the film, and a lowering of the "stickness" of the cut and stacked sheets.
[0032] The protective film obtained with a paint of this type has a low resistance to arc discharge in a thickness interval comprised between 2.5 and 3.5 µm. Such thicknesses allow in fact a point welding with discharges of 6 V at 10,000 A, with a negligible formation of fumes and carbon depositions.
[0033] Our polymer is obtained by the copolymerisation of 4 monomers, has an average molecular weight (Mw) between 5,000 and 50,000, in particular between 8,000 and 15,000 and a mEq. value in the dry state of between 30 and 100, in particular between 50 and 60.
[0034] Furthermore, it shows a viscosity (Brookfield) in a 50% solution 1/1 in butylglycol/water of between 1,500 and 150,000 mPa·s, at 20°C, in particular of between 2,500 and 6,000 mPa·s at 20°C.
[0035] The introduction in the paint of a polymeric wax with a melting point of between 75 and 110°C, in particular of between 93 and 99°C, a hardness (ASTM-D.5) of between 2 and 3, in an amount of between 1 and 40%, in particular 1 and 10% on the paint solids determines a very low friction coefficient which allows to stamp the sheets without seizure of the stamps.
[0036] A paint thus obtained may be employed in traditional ways (dip-coating, flow-coating, coil-coating, spraying): however, the best results are obtained by the electrophoretic process according to the invention.
[0037] An acrylic polymer which may be used in the preparation of a protective paint is produced as follows.
[0038] Butylglycol, 165.2 parts and isopropyl alcohol, 10.11 parts (all parts by wt.) are charged in a reaction vessel equipped with stirrer, temperature control means, container for the addition of monomers, condenser and with a means apt to maintain the reagents in a nitrogen atmosphere.
[0041] A mixture of monomers A is prepared in the meantime, having the following composition by wt.:
| Ethyl acrylate | 108.49 |
| Butyl acrylate | 95.92 |
| Methyl methacrylate | 114.64 |
| Styrene | 69.90 |
| Methacrylic acid | 76.81 |
| Tertiary Dodecylmercaptane | 0.93 |
[0043] A mixture B is then prepared in another vessel, consisting of:
| Butylglycol | 65.21 parts by wt. |
| Tert.butyl perbenzoate | 6.47 parts by wt. |
[0044] At this point, 46 parts by wt. of mixture A are introduced in the reaction vessel and the temperature is brought to 135°C.
[0046] Once this addition is completed, the rest of mixture B is added within one hour, always keeping the temperature at 135°C. The heating at 135-137°C is maintained for an hour.
[0047] Then, vacuum is applied and approximately 75 parts by wt. of solvent are extracted. The vessel is then cooled to 95-100°C and 270.13 parts by wt. of butylglycol are added.
[0049] After stirring for 3 hours at that temperature, the characteristics of the mixture are controlled. They should be:
| Dry residue: | 50 ± 1 (30' at 180°C) |
| mEq.: | 58-60 on the solids |
| Viscosity: | 3,000 - 5,000 cps (Brookfield) |
| Na: | 95-110 on the solids |
| PMW: | approximately 10,000 |
[0050] A paint for the temporary protection of metal coils utilizing the preceding resin is prepared as follows:
to 730g of resin solution prepared as described, 50g of a polymeric wax dispersing with 18% active substance, melting point 93-99°C and average particle diameter 2-5 µm are added, stirring rapidly for 10'.
[0051] Then 100g butylglycol and 100g demineralized water are added under stirring, and under slow mixing, diisopropylamine to pH 8.
[0052] While with the traditional electrodeposition equipment it was impossible to obtain satisfactory results in the painting of coils with such a strict tolerance (0.5 µm) on the thickness of the coat, with the process which is an object of the present application perfectly homogeneous paint layers (3.5 µm) are obtained which are within the tolerance.
[0053] In fact, with the use of traditional counter-electrodes, consisting essentially of a plate of stainless steel, a thickening of the electric field on the electrode edges takes place. Because of this, the paint layers along the coil edges are thicker than the layers at the centre. This lack of homogeneity is the cause of the mentioned serious inconveniences.
[0054] The newly conceived counter-electrode which is employed in the electrophoresis apparatus and relative process which are objects of the present invention, consists in its preferred but not limitative embodiment, of a rectangular metal plate, generally of stainless AISI 316 steel, in which holes are punched.
[0055] Instead of plates, cylinders may be used as counter-electrodes, obtained by rolling on themselves metal bands on which the holes and the points associated with them are located.
[0056] To each hole at least one point is associated, protruding in the direction of the coil to be painted. Around the holes a thickening of the electric charges takes place which flow toward the point; the tension difference between the points on the counter-electrode and the coil thus provides a perfectly homogeneous electric field. This provides for a perfect paint deposition on the coil.
[0057] The points may also be more than one for each hole: a very advantageous embodiment of the invention provides points formed while punching the holes: by making cross-cuts in the locations where the holes are wished, four triangular sectors are obtained which are pushed outside to form the points.
[0058] More than four points can be obtained employing a similar technique. To this regard, the punching of the plate is very advantageous in order to obtain at the same time both the holes and the protruding points.
[0059] Each line of holes and of points may be staggered with respect to the two adjacent ones, thus obtaining an electric field as uniform as possible.
[0060] A same inventive conception includes all electrodes providing for any plurality of points, with or without adjacent holes, which protrude from the main electrode surface thus creating a uniform electric field.
[0061] The present invention concers an apparatus and a related process for the electrophoretic painting of metal structure, in particular of metal sheet coils.
[0062] It consists of at least one electrode on which the structure is electrically charged, at least one tank containing the paint, at least two counter-electrodes having a polarity opposite to the one of the electrode dipped into the paint bath, at least one over-flow tank in which the metal structure is washed, at least one oven for the polymerization and at least one cooling system.
[0063] The apparatus and process are characterized in that said at least two counter electrodes consist of at least two metal elements situated on opposite sides with respect to the metal structure and that on each of the elements there is at least a series of holes associated with a series of metal points directed toward the metal structure in order to obtain on it a uniform electric field.
LIST OF FIGURES
[0064] Fig. 1 shows, in a cross-section, the plant for the electrophoretic painting which is an object of the present invention. For simplicity's sake, anodic electrophoresis is considered; however, similar statements may be made in connection with cathodic electrophoresis.
[0065] Fig. 2 shows a plan view of the plant of Fig. 1, to which other elements not present in Fig. 1 have been added.
[0067] For simplicity, a planar counter-electrode is shown, but similar considerations will apply to cylinder counter-electrodes or counter-electrodes of any other shape.
DETAILED DESCRIPTION
[0068] In Figs. 1 and 2, as an illustrative, non limitative example, a plant for anaphoretic electrodeposition is shown. 1 indicates the tank where the paint electrodeposition on the coil is carried out: it is normally made out of PVC coated steel. Next to tank 1 is an overflow tank 5 with circulation pumps 17 and an ultrafiltration station 6.
[0069] To roller 4 a hole is connected, which in the case of anaphoresis (as in the figure) is positively charged (anode) and positively charges coil 19. The electrically insulated roller 2 guides the coil 19 into the tank 1: the roller idles on the shaft and is cooled inside. Counter-electrodes 3,20, which, in the case represented by the figure, are negatively charged (cathodes) dip into tank 1; in a preferred, non limitative, embodiment each of them consists of a plate 21 (Figs. 3 and 4), generally of AISI 316 stainless steel, on which holes 22 are bored; to each of the holes at least one point 23 corresponds which protrudes toward coil 19 to be painted. Around holes 22 electric charges concentrate flowing toward points 23; in this way, a perfectly homogeneous electric field is created between negative counter-electrode 3,20 and coil 19.
[0071] Normally a three-phase, 380V, 50 Hz current is fed, which at the exit is adjusted at between 30 and 400 V depending on the bath conditions. The highest current in a continous service is approximately 400 A.
[0072] The coil, up to 2,000 mm wide, runs at the rate of 70 m/minute. This rather high speed requires a high "penetration" of the counter-electrodes in order that the coil be covered in a few seconds with a constant thickness (3 ± 0.5 µm) of protective paint.
[0073] The applicant has now found that the best results with regard to the "penetration" are obtained when:
| (for plate counter-electrodes): | |
| Hole diameter | D = 10-20 mm |
| Distance from the edge of the first series of holes | 1 = 25-50 mm |
| Distance between two hole series (pitch) | p = 50-100 mm |
| Nr. of holes per sq decimetres | N1 = 4-9 |
| Ratio between full/hollow areas | (1/0.03)-(1/0.28) |
| Point heigth | h = 1-3 mm |
| Nr. of points around each hole | N2 = 3-4 |
| (for cylindrical counter-electrodes): | |
| Counter-electrode diameter | D1 = 60-150 mm |
| Hole diameter | D2 = 10-20 mm |
| Distance between two hole series (pitch) | p = 50-100 mm |
| Nr. of holes in each series | N1 = 4-8 |
| Nr. of holes with points in each series | N2 = 3 |
| Point heigth | h = 1-3 mm |
| Nr. of points around each hole | N2 = 3-4 |
| Ratio between full/hollow areas | (1/0.03)-(1/0.28) |
[0074] Through experimental tests the applicant has furthermore found that, in case cylindrical counter-electrodes are employed, only the ones facing the coil must be provided with points.
[0076] The washing operation is very important; in fact, the coil 19, covered by perfectly compact and adhering paint layer, drags out of the tank physically adherent, non-electrodeposited portions of the bath which must be removed. The washing is made first with tap water, followed by rinsing with demineralized water or by ultrafiltration. Normally, ultrafiltration is employed which requires less water and allows to recover a considerable amount of paint, which otherwise would be lost.
[0077] For the ultrafiltration, a permeable membrane on a support is employed, through which the electrophoresis bath is passed, at a rate of 2-3 m/sec. under a 2 to 4 bar pressure, tangentially to one side of the membrane; the heavier paint particles adhere to the membrane, while water, neutralizing agents, soluble salts, solvents and fractions of resin go through and are returned to the rinsing nozzles 14.
[0079] The plant further comprises dialysis cells 11 for controlling the neutralizing agent contents in the bath; the cells 11 consist of a semipermeable membrane placed in front of the counter-electrodes forming a cell; only the neutralizer ions go through, while colloidal resin particles present in the bath are stopped. The neutralizer ions go by dialysis through the membrane and are then removed by a controlled flow of demineralized water which starts as the cell conductivity reaches a predetermined value.
[0080] After the wash, the coil goes through a polymerisation furnace where in 5 sec. a temperature of 180°C is reached. An infrared furnace is suitable for this purpose.
[0082] It is very important to keep the paint bath at a constant temperature (about 25° C), and to that end heat-exchangers 10 are provided to cool the paint which tends to heat up by Joule effect.
[0083] The plant is completed by a group 8 for the continuous refilling of the paint, a group 9 of paint tanks, a current rectifier group 12 and electric service and regulation boards 13.
[0084] The painting process, in the case of anaphoresis takes place as follows:
A - The coil 19, which can be up to 2,000 mm wide, is passed at the rate of 70 m/minutes through tank 1 which contains the cited type of paint; it is positively charged (in the case of anaphoresis) on roller 4, is deviated by roller 2, which is electrically insulated and internally cooled, and pushed into the bath.
B - The coil passes through counter-electrodes 3 negatively charged (in anaphoresis), of the type claimed according to the present invention, where the electrodeposition takes place.
C - The coil passes in overflow tank 5 where it is washed with ultrafiltered water by nozzles 14; thus paint particles, which are dragged out but not electrodeposited on the coil, are washed out.
D - The coil goes through the polymerization furnace 15 where, at 180°C, the paint film is polymerized in 5 sec..
E - The coil is cooled in 16.
[0085] The applicant successfully experimented the newly conceived electrodes in traditional plants for electrophoretic painting (in substitution of the previous plate electrodes without holes or metal points) obtaining the following results:
1 - Test OLMO MOTORS
2 - Test WARM
1. An apparatus for the electrophoretic painting of metal structures (19) in particular
for the electrophoretic painting of metal sheet coils, comprising at least one electrode
(4) on which said structure (19) is electrically charged, at least one tank (1) containing
a paint bath (18), at least two counter-electrodes (3, 20) dipped into said bath (18)
having a polarity opposed to the one of said at least one electrode (4), an overflow
tank (5) in which said structure (19) undergoes washing, a polymerization furnace
(15) and finally a cooling device (16), the apparatus being characterized in that
said at least two counter-electrodes (3; 20) consist of at least two metal elements
(21) situated on opposite sides with respect to the metal structure (19), and that
on each of said elements (21) there is at least a first series of holes (22) associated
to at least a second series of metal points (23) directed toward said structure (19)
so as to create on it a uniform electric field.
2. An apparatus as claimed in claim 1, characterized in that said at least one electrode
(4) is positively charged, and that said at least two counter-electrodes (3,20) are
negatively charged.
3. An apparatus as claimed in claim 1, characterized in that said at least one electrode
(4) is negatively charged and that said at least two counter-electrodes (3,20) are
positively charged.
4. An apparatus as claimed in claims 1, 2 and 3, characterized in that said elements
(21) are plates.
5. An apparatus as claimed in claims 1, 2 and 3, characterized in that said elements
(21) are cylinders.
6. An apparatus as claimed in claims 1, 2, 3, 4 and 5, characterized in that said holes
(22) and said points (23) are obtained by punching of plates (21).
7. An apparatus as claimed in claim 1, characterized in that it comprises a device (2)
apt to dip the structure (19) in the bath (18).
8. An apparatus as claimed in claim 7, characterized in that said device (2) is situated
between said first means (4) and said second means (3) and consists of a mouvable
roller, which is electrically insulated and internally cooled.
9. An apparatus as claimed in claims 1-8, characterized in that said structure (19) moves
forward at the speed of 70 m/minutes.
10. An apparatus as claimed in claims 1-9, characterized in that said polymerization furnace
(15) heats said structure to 180°C in 5 sec.
11. A process for the electrophoretic painting of metal structures, in particular of metal
sheet coils, in which said structure is passed first on at least one electrode on
which it is electrically charged, and right after between at least two counter-electrodes
dipped in the paint bath and having a polarity opposite to the one of said at least
one electrode; in which said structure passes into a overflow tank in correspondence
of which it undergoes a washing; in which said structure goes through a polymerization
oven and finally through a coil device, the process being characterized in that said
at least two counter-electrodes consist of at least two metal elements situated on
opposite sides of the structure and that on each of said elements there is at least
a first series of holes associated with at least one series of metal points directed
toward said structure in order to realize in it a uniform electric field.
12. A process as claimed in claim 11, characterized in that it is a process for anaphoretic
painting.
13. A process as claimed in claim 11, characterized in that it is a process for cathaphoretic
painting.
14. A process as claimed in claim 11, characterized in that said elements consist of plates.
15. A process as claimed in claim 11, characterized in that said elements consist of cylinders.
16. A process as claimed in claim 11, characterized in that it employs a paint bath produced
as follows:
in a reaction vessel, equipped with stirrer, temperature control means, container for the monomers to be added, condenser and means to keep the reagents in a nitrogen atmosphere, 165.2 parts by wt. butylglycol and 10.11 parts by wt. isopropyl alcohol are charged, equipping the vessel for direct recycling of the solvent; the vessel is heated on reflux under stirring and in a nitrogen atmosphere, to 140°C; in the meantime a mixture of monomers A is prepared as follows (parts by wt.):
The acidity number is controlled and adjusted to 110-111 by addition of methacrylic
acid; in another container a mixture B is prepared made out of:
then, 46 parts by wt. of mixture A are introduced in the reaction vessel and the
temperature is brought to 135°C; then the residue of mixture A is added, always with
direct recycling, with the addition of 55 parts by wt. of mixture B; this operation
should be completed in 6 hours; then the rest of mixture B is added in 1 hour time,
keeping the temperature at 135°C;
this temperature is kept for an hour longer at 135°C-137°C;
then, under vacuum, approximately 75 parts by wt. of solvent are distilled off; after cooling to 95-100°C, 270.13 parts by wt. butylglycol are added, and then at 50°C, 16-18 parts by wt. of 28 Bé ammonia are further added to the mixture;
that temperature is kept under stirring for 3 hours, then the prescribed data are controlled which should be:
to 730 g of the resin solution thus prepared, 50g of a dispersion of a polymeric
wax with 18% active substance of melting point 93-99°C and average particle diameter
2-5 µm are added, stirring rapidly for 10'; under stirring, 100g butylglycol and 100g
demineralized water are added, then di-isopropylamine up to pH 8, under low mixing.
in a reaction vessel, equipped with stirrer, temperature control means, container for the monomers to be added, condenser and means to keep the reagents in a nitrogen atmosphere, 165.2 parts by wt. butylglycol and 10.11 parts by wt. isopropyl alcohol are charged, equipping the vessel for direct recycling of the solvent; the vessel is heated on reflux under stirring and in a nitrogen atmosphere, to 140°C; in the meantime a mixture of monomers A is prepared as follows (parts by wt.):
| Ethyl acrylate | 108.49 |
| Butyl acrylate | 95.92 |
| Methyl methacrylate | 114.64 |
| Styrene | 69.90 |
| Methacrylic acid | 76.81 |
| Tert.dodecilmercaptane | 0.93 |
| Butylglycol | 65.21 by wt. |
| Tert.butylperbenzonate | 6.47 |
this temperature is kept for an hour longer at 135°C-137°C;
then, under vacuum, approximately 75 parts by wt. of solvent are distilled off; after cooling to 95-100°C, 270.13 parts by wt. butylglycol are added, and then at 50°C, 16-18 parts by wt. of 28 Bé ammonia are further added to the mixture;
that temperature is kept under stirring for 3 hours, then the prescribed data are controlled which should be:
| Dry residue: | 50 ± 1 (30' to 180°C) |
| mEq.: | 58-60 on the solids |
| Viscosity: | 300-500 mPa·s (Brookfield) |
| Na: | 95-110 on the solid |
| PMW by wt.: | ca. 10,000 |
17. A process as claimed in claim 11, characterized in that the metal structure goes through
the paint bath at the rate of 70 m/minutes.
18. A process as claimed in claim 11, characterized in that said polymerization furnace
heats up the metal structure to 180°C within 5 sec.
19. A process as claimed in claim 11, characterized in that between said at least one
electrode and said at least two counter-electrodes a tension of 150 V is applied.
20. A process as claimed in claim 11, characterized in that between said at least one
electrode and said at least two counter-electrodes a tension of 400 V is applied.
21. A process as claimed in claim 11, characterized in that the electro-applied paint
film has a thickness of 3 ± 0.5 µm.