Classifications

• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
  • B05C—APPARATUS FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
  • B05C19/00—Apparatus specially adapted for applying particulate materials to surfaces
  • B05C19/02—Apparatus specially adapted for applying particulate materials to surfaces using fluidised-bed techniques
  • B05C19/025—Combined with electrostatic means

Definitions

• Soaking in a known fluidized electrostatic bath presents a non-negligible risk of electric arc between the substrate to be coated connected to the ground and the conductive electrode which can cause the pulverulent mass of the tank to ignite and / or explode. Because of these risks, it is dangerous to completely immerse the substrates to be coated within the pulverulent mass in fluidization and therefore requires the use of a minimum quantity of powder.
• this technique only allows regular and uniform coating of substrates of small size and very simple geometry such as wires, cables or profiles.
• DD 242.353 a method of soaking in a fluidized electrostatic bath has been described in which the charging electrode is a semiconductor electrode laminated to an insulator. This system makes it possible to limit the risks of ignition and explosion of the pulverulent mass which is located within the tank; however, for complex and fairly large parts, the coating is neither regular nor uniform.
• the electrostatic fluidized bath according to the invention consists of a tank made of insulating material, for example polyvinyl chloride (PVC), polypropylene (PP), polyethylene (PE), polytetrafluoroethylene (PTFE), polyvinylidene fluoride (PVDF) more often parallelepipedal, or cylindrical.
• PVC polyvinyl chloride
• PP polypropylene
• PE polyethylene
• PTFE polytetrafluoroethylene
• PVDF polyvinylidene fluoride
• the semiconductor electrodes (8) according to the invention have a volume resistivity between 1 ⁇ 2 and 10 8 ⁇ .m, and preferably between 10 4 and 10 6 ⁇ .m measured according to standard ASTM D257.
• the conductive particles or charge centers can be based on carbon black, metallic oxides, powders of metallic compounds (Fe, Al, Zn, Ni, Cu, bronze, brass, ...), graphite, and generally any additive with a volume resistivity much lower than that of the insulating matrix.
• a stabilized high voltage generator (7) delivering an adjustable voltage between 0 and 60 kV, positive or negative of low amperage (generally less than 200 ⁇ A) via a junction contact (10 ) placed at the back of the electrode, that is to say on the side facing the wall of the tank.
• the junction contact can be punctual; in this case, we prefer to place it in the upper rear part of the electrode.
• the electrical contact at the level of the electrode is not ensured by a conductive element dangerous to the operators during an unexpected disconnection but is ensured by means of a semiconductor element which extends beyond the tank, thus eliminating any risk of electric shock in the vicinity of the tank.
• Another preferred embodiment of the electrode according to the invention consists in applying to the rear face of the electrode described above an element of lower resistivity (11), therefore more conductive, for example by gluing, co-extrusion, etc. . This more conductive element can completely or partially cover the rear face of the electrode.
• This composite electrode makes it possible to improve the distribution of charge carriers on the surface of the charge electrode, ie on the face in contact with the powders.
• the electrodes according to the invention can be independent or integral with the fluidization tank. In the latter case, they can be fixed to the vertical walls of the tank and / or to the porous bottom.
• the electrodes are independent of the fluidized bath, they can be subjected to vibratory movements intended to peel off the clumps of powders, when the electrodes are integral with the tank, the tank + electrode (s) assembly can be subjected to a mechanical vibration system.
• substrates As an example of substrates, mention may be made of metallic substrates or those comprising a metallic part, for example iron, ordinary or galvanized steel, aluminum or aluminum alloy, wooden, plastic, glass substrates , cement, terracotta, and generally composite materials of which at least one of the elements can be chosen from the previous list.
• metallic substrates for example iron, ordinary or galvanized steel, aluminum or aluminum alloy, wooden, plastic, glass substrates , cement, terracotta, and generally composite materials of which at least one of the elements can be chosen from the previous list.
• the substrate Prior to coating powders, the substrate can undergo one or more surface treatments such as alkaline degreasing, pickling, brushing, shot blasting, phosphating, hot rinsing, etc.
• surface treatments such as alkaline degreasing, pickling, brushing, shot blasting, phosphating, hot rinsing, etc.
• certain surface treatments which degrade at high temperature can be used, namely phosphating Fe, Zn, galvanization, as well as prior coating using primer.
• an adhesion primer can be applied either in liquid form in pulverulent form.
• the coating powders which can be used in the context of the present invention can constitute the adhesion primer and / or the surface coating; they have a volume resistivity between 10 12 and 10 17 ⁇ .m and preferably between 10 13 and 10 16 ⁇ .m.
• the volume resistivity of the powders is measured using a resistivity cell whose electrometer has a resistance greater than 10 ⁇ ⁇ .
• a powder height of 1 cm is placed in the cell after tamping, a voltage V of 1 kV is applied to the cell and the intensity I of the current flowing through the cell is measured.
• the powders according to the invention are based on plastics or thermoplastic and / or thermosetting resins.
• polyolefins such as PE, PP, their copolymers or alloys
• thermosetting resins there may be mentioned
• the surface coating can be applied in another fluidized bath according to the invention without first filming it by intermediate cooking.
• a primer in liquid form it is preferable to allow it to dry for a few minutes, for example at room temperature, before soaking in the fluidized bath according to the invention.
• the tank can be kept stationary and the substrate to be coated is immersed in the pulverulent mass which is maintained under rotating, ascending, descending, etc. agitation.
• the substrate can also be kept stationary and by an appropriate lever system of the fluidization tank lift said tank until the substrate is immersed in the pulverulent material and ensure stirring of the powder bath by means of a system of vibration of the tank.
• the fluidized bath and the electrodes are as shown in the Figure.
• the substrate to be coated is immersed vertically (the long side (3 meshes) of the mesh is immersed perpendicular to the bottom of the tank) in a fluidized bath in which there are also 2 semiconductor electrodes (see Fig) and with volume resistivity 10 4 -10 ⁇ ⁇ .m; the rear face of this electrode is made of a volume resistivity material 10 3 -10 ⁇ ⁇ .m laminated.
• the substrate to be coated is immersed in an electrostatic fluidized bath in which there are 2 semiconductor electrodes with a volume resistivity 10 4 -1 ⁇ 6 ⁇ .m the rear face of which is partially laminated on which we laminated insulating material according to DD 242.353.
• the voltage applied to the electrodes is +8 kV.
• the soaking time of the substrate which is necessary for the thickness of the coating in the center of the mesh is equal to 130 ⁇ m is measured and the coating thicknesses are determined on the periphery of the mesh (at the 4 vertices and in the middle of the 4 sides).
• the substrate consists of a steel plate with a side of 3 mm thick and 3 mm thick. It is coated under the same operating conditions as that of the substrate of Example 1 (same coating powders; thickness of the coating at the center of the part: 130 ⁇ m) and the thickness of the coating is measured at the 4 vertices of the room.
• the wire mesh thus coated is cooked by passing through an oven at 220 ° C. for 5 minutes. Uniform coating is obtained as well as excellent covering of the wires, in particular at the intersections of the mesh with a very good appearance of the coating.
• the mesh is coated with powders with the same characteristics as those of Example 1, under similar operating conditions (soaking time: 3 sec; voltage applied to semiconductor electrodes: +10 kV).
• the wire mesh thus coated is cooked by passing through an oven at 220 ° C. for 5 minutes. Uniform coating is obtained as well as excellent covering of the wires, in particular at the intersections of the mesh with a very good appearance of the coating.
• Example 1 We proceed to the surface coating of a mesh as defined in Example 1 with powders of volume resistivity 3.10 ' ' 0 ⁇ .m and made of PA-6 in the form of microporous beads of average diameter 40 ⁇ m and maximum diameter less than 80 ⁇ m, viscosity in solution of approximately 0.83 dl / g in a fluidized bath as described in Example 1 followed by baking in the oven.
• Example 1 One proceeds to the coating of a mesh as defined in Example 1 with powders of volume resistivity 8.10 ⁇ 4 ⁇ .m and consisting of ethylene / acrylic acid copolymer containing 7% by weight of acrylic acid, diameter medium 100 ⁇ m and maximum diameter less than 300 ⁇ m in a fluidized bath as described in Example 1 and under similar operating conditions (soaking time: 6 s; voltage applied to the semiconductor electrode: +10 kV ).
• EXAMPLE 8 A mesh as defined in Example 1 is coated with powders with a volume resistivity greater than 10 ⁇ ⁇ .m and consisting of 100 parts by weight of PA-11 with a viscosity in solution of approximately 1 , 15 dl / g, with an average diameter of 100 ⁇ m, a maximum diameter of less than 300 ⁇ m and of which 1% by weight of the particles has a diameter of less than 40 ⁇ m and 0.05 parts by weight of fluidizing agent in a bath fluidized as described in Example 1 and under similar operating conditions.
• the PA-11 used was polymerized in the presence of H3PO4 while the PA-11 of Examples 1, 2, 4 were polymerized in the presence of H3PO2.
• Example 8 After coating with a mesh as defined in Example 1 using a liquid primer of the epoxy / phenolic type with a thickness of 10-15 ⁇ m, it is left to dry for 15 min at room temperature before proceeding with the surface coating. roasting with powders consisting of * 100 parts by weight of PA-11 of Example 8,
• EXAMPLE 10 After coating with a wire mesh as defined in Example 1 using a powdered primer of the epoxy / dicyandiamide type in stoichiometric proportions using an electrostatic gun (voltage +30 kV), the mesh is surface coated with powders of the same characteristics as those of Example 9 under similar operating conditions (soaking time: 10 s; voltage applied to the semiconductor electrode: +15 kV).
• the mesh thus coated is then baked by passage through an oven at 200 ° C for 5 minutes.
• a uniform deposit of the coating with a thickness of between 160 and 300 ⁇ m is obtained as well as an excellent covering of the wires, in particular at the intersections of the mesh with very good filming of the coating.
• the substrate consists of a mesh of dimension 100 * 150mm obtained by welding at right angles to degreased ordinary steel wire and shot of diameter 3.25 mm, the mesh size of the mesh being 50 * 50 mm. It is coated under the same operating conditions as that of the substrate of Example 1 (same coating powders; coating thickness at the center of the part: 130 ⁇ m) except for the 2 semiconductor electrodes which have a volume resistivity less than 10 4 ⁇ .m and were produced by the applicant by incorporating carbon black into natural rubber. An electric arc occurs when the distance between the tips of the electrodes and the substrate is less than 5 cm, the voltage applied to the electrodes being +8 kV.

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• Application Of Or Painting With Fluid Materials (AREA)
• Electrostatic Spraying Apparatus (AREA)

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• 1994
  • 1994-06-08 FR FR9407214A patent/FR2720959B1/fr not_active Expired - Fee Related
• 1995
  • 1995-06-08 WO PCT/FR1995/000751 patent/WO1995033576A1/fr not_active Application Discontinuation
  • 1995-06-08 CA CA002192000A patent/CA2192000C/fr not_active Expired - Fee Related
  • 1995-06-08 EP EP95922582A patent/EP0764058A1/de not_active Ceased
  • 1995-06-08 JP JP8500466A patent/JPH10501298A/ja active Pending

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