Classifications

• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B23—MACHINE TOOLS; METAL-WORKING NOT OTHERWISE PROVIDED FOR
  • B23K—SOLDERING OR UNSOLDERING; WELDING; CLADDING OR PLATING BY SOLDERING OR WELDING; CUTTING BY APPLYING HEAT LOCALLY, e.g. FLAME CUTTING; WORKING BY LASER BEAM
  • B23K35/00—Rods, electrodes, materials, or media, for use in soldering, welding, or cutting
  • B23K35/22—Rods, electrodes, materials, or media, for use in soldering, welding, or cutting characterised by the composition or nature of the material
  • B23K35/36—Selection of non-metallic compositions, e.g. coatings, fluxes; Selection of soldering or welding materials, conjoint with selection of non-metallic compositions, both selections being of interest
  • B23K35/362—Selection of compositions of fluxes
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B23—MACHINE TOOLS; METAL-WORKING NOT OTHERWISE PROVIDED FOR
  • B23K—SOLDERING OR UNSOLDERING; WELDING; CLADDING OR PLATING BY SOLDERING OR WELDING; CUTTING BY APPLYING HEAT LOCALLY, e.g. FLAME CUTTING; WORKING BY LASER BEAM
  • B23K35/00—Rods, electrodes, materials, or media, for use in soldering, welding, or cutting
  • B23K35/22—Rods, electrodes, materials, or media, for use in soldering, welding, or cutting characterised by the composition or nature of the material
  • B23K35/36—Selection of non-metallic compositions, e.g. coatings, fluxes; Selection of soldering or welding materials, conjoint with selection of non-metallic compositions, both selections being of interest
  • B23K35/3601—Selection of non-metallic compositions, e.g. coatings, fluxes; Selection of soldering or welding materials, conjoint with selection of non-metallic compositions, both selections being of interest with inorganic compounds as principal constituents
  • B23K35/3603—Halide salts
  • B23K35/3605—Fluorides
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B23—MACHINE TOOLS; METAL-WORKING NOT OTHERWISE PROVIDED FOR
  • B23K—SOLDERING OR UNSOLDERING; WELDING; CLADDING OR PLATING BY SOLDERING OR WELDING; CUTTING BY APPLYING HEAT LOCALLY, e.g. FLAME CUTTING; WORKING BY LASER BEAM
  • B23K35/00—Rods, electrodes, materials, or media, for use in soldering, welding, or cutting
  • B23K35/22—Rods, electrodes, materials, or media, for use in soldering, welding, or cutting characterised by the composition or nature of the material
  • B23K35/36—Selection of non-metallic compositions, e.g. coatings, fluxes; Selection of soldering or welding materials, conjoint with selection of non-metallic compositions, both selections being of interest
  • B23K35/3612—Selection of non-metallic compositions, e.g. coatings, fluxes; Selection of soldering or welding materials, conjoint with selection of non-metallic compositions, both selections being of interest with organic compounds as principal constituents
  • B23K35/3613—Polymers, e.g. resins
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B23—MACHINE TOOLS; METAL-WORKING NOT OTHERWISE PROVIDED FOR
  • B23K—SOLDERING OR UNSOLDERING; WELDING; CLADDING OR PLATING BY SOLDERING OR WELDING; CUTTING BY APPLYING HEAT LOCALLY, e.g. FLAME CUTTING; WORKING BY LASER BEAM
  • B23K2103/00—Materials to be soldered, welded or cut
  • B23K2103/08—Non-ferrous metals or alloys
  • B23K2103/10—Aluminium or alloys thereof
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B23—MACHINE TOOLS; METAL-WORKING NOT OTHERWISE PROVIDED FOR
  • B23K—SOLDERING OR UNSOLDERING; WELDING; CLADDING OR PLATING BY SOLDERING OR WELDING; CUTTING BY APPLYING HEAT LOCALLY, e.g. FLAME CUTTING; WORKING BY LASER BEAM
  • B23K35/00—Rods, electrodes, materials, or media, for use in soldering, welding, or cutting
  • B23K35/22—Rods, electrodes, materials, or media, for use in soldering, welding, or cutting characterised by the composition or nature of the material
  • B23K35/34—Rods, electrodes, materials, or media, for use in soldering, welding, or cutting characterised by the composition or nature of the material comprising compounds which yield metals when heated

Definitions

• the invention relates to an aluminium product having excellent brazing characteristics having at least one flat surface coated with a brazing flux composition comprising brazing flux and a synthetic resin based, as its main constituent, as methacrylate homopolymer or a methacrylate copolymer.
• Such an aluminium product is known from GB-A-2.334.531.
• the coating contains braze particles, especially metallic particles or Si-particles or mixtures thereof, in order to obtained the required brazing connection.
• braze particles have a number of disadvantages.
• braze particles In the first place the braze particles must be mixed with the binder of the coating, which is in fact a physical mixture and therefore subject to separation and loss of homogenity in the coating.
• the size of the braze particle tends to be large in relationship to the coating thickness so that particles stand proud of the coated surface thereby causing a roughened surface which will inhibit sliding of tubes during handling.
• mechanical abrasion can take place between contacting surfaces of two products during handling, transport machining etc., thereby changing or even destroying the brazing characteristics of the applied coating.
• braze particles and especially of Si-particles can give localised surface reactions which lead to irregular thinking of the surface of the product during brazing, or the generation of brazing faults such as burn through.
• brazing flux is a reactive flux and in that the coating of brazing flux is free from metal and / or silicon particles.
• a reactive flux is a flux which contains a chemical composition which as result of the reaction between aluminium and the chemical composition at elevated temperature results in in situ formation of a brazing alloy which can be brazed at that temperature.
• the reactive flux is a fluorosilicate or potassiumfluorozudie of potassium but caesium or rubidium salts are also effective.
• the weight ratio of the brazing flux to the synthetic resin in the flux composition is in the range from 9:1 to 3:2.
• the weight ratio of the reactive flux exceeds 9, adhesion of the composition to the aluminium material becomes insufficient and the coating tends to cause flaking, whereas at less than 3:2 the excessive proportion synthetic resin can harm the brazing atmosphere which alter braze characteristics and raise the cost.
• the invention also relates to a method for manufacturing an aluminium product having excellent brazing characteristics having at least one flat surface which is coated with a mixed flux composition comprising a brazing flux and as organic solvent in which a synthetic resin based, as its main constituent, on a methacrylate homopolymer or a methacrylate copolymer is dissolved.
• brazing flux is a reactive flux
• the coating of brazing flux is free from metal and / or silicon particles
• the coating is applied by means of a reverse roll coating technique, whereupon the applied coating is heated and dried to evaporate the organic solvent in the mixed flux composition.
• Roll-transfer printing can also be used as an application method but reverse roll coating is preferred since it offers superior control of the quality of the deposited layer.
• the synthetic resins to be used in the present invention those mainly comprising a homopolymer of a methacrylate or a copolymer of two or more methacrylates are preferred.
• a methacrylic acid ester examples include methyl methacrylate, ethyl methacrylate, propyl methacrylate, 2-methylpromyl methacrylate, n-butyl methacrylate, t-butyl methacrylate, 2-etylhexyl methacrylate, octyl methacrylate : isodecyl methacrylate, lauryl methacrylate, tridecyl methacrylate, stearyl methacrylate, cyclohexyl methacrylate, benzyl methacrylate, diathylaminoethyl methacrylate, 2-hydroxyethyl methacrylate, dimethylaminoethyl methacrylate, t-butyla
• Reverse roll coat or roll-transfer printing equipment for example has a configuration illustrated in Figure 1 , wherein an aluminium-extruded multi-cavity flat tube A supplied from a rewinding unit 8 is sent to a composition application step via a feeder roll 10.
• the composition stored in a composition container 1 is picked up by an attached pick-up roll 2, transferred to an application roll 3, and then applied to the surface of the aluminium-extruded multi-cavity flat tube A that passes through the application roll 3 and a back-up roll 4.
• the aluminium-extruded multi-cavity flat tube A coated with a composition is sent through a feeder roll 11 to an oven 5 such as a convection oven that consists of a drying zone 6 and a cooling zone 7.
• the aluminium-extruded multi-cavity flat tube A after being heated in the drying zone 6 to a temperature of about 200° to 300°C, is cooled and wound up by a winder unit 9, after passing through a feeder roll 12.
• a convection heating system is suitable as the heating system for the furnace, radiant heating with far-infrared rays could also be used, in conjuction with a supply of air to promote evaporation of organic solvents.
• the aluminium-extruded multi-cavity flat tube A passes through the furnace 5 usually within several seconds during which time the organic convents contained in the composition coated on it evaporate, leaving a coating comprising flux and synthetic resin, on one of the flat surfaces of the aluminium-extruded multi-cavity flat tube.
• Figure 1 illustrates the equipment configuration for applying a composition on just one side of the flat surface of the aluminium-extruded multi-cavity flat tube, both sides of the flat tube can be coated by adding one more composition container and roll set.
• the binder system was based upon Paraloid B 48 (Rohm & Haas). A flux to binder ratio of 3:2 was found satisfactorily from a brazing aspect and a coating was produced. A batch of K j SiFg was used in the trials. This material was synthesised and screened to ensure that maximum particle size would be less than the dry coating thickness of the coating on the tube. (i.e. ⁇ 30 ⁇ m) The Paraloid B 48 was available in a 40% solids solution in Xylene solvent. The bar coat trials to adjust coating parameters are summarised below:
• MPE tube samples were coated using the 036 bar coater. Drying / cure of the wet coating utilised the standard oven setting, i.e. 1 1/2 minutes in oven set at 240°C. The dry film thickness was confirmed as 25 to 28 ⁇ m when checked using an eddy current coating thickness measuring device. Reverse impact tests using 60, 40 and 20 Ib.in. showed no loss of adhesion on the indentation and no loss of coating when tested with adhesive tape (Sellotape). Coated tube samples were subjected to a flat bend and again the adhesion was tested by means of adhesive tape. Only a slight discolouring of the tape was observed. The surface of the dry coating was relatively smooth and did not show any tendency to stick to adjacent coated surfaces. Tubes coated in the manner described above were assembled with unclad fins and brazed successfully in a CAB braze oven.
• Sufficient coating material was made up to fill the tray of a laboratory roll coat equipment. In all, about 2 litres of coating was made up according to the 3:2 flux to Paraloid B 48 ratio.
• the solvent used for the B 48 was DBE (dibasic ester).
• the coater was set up in 2 roll conformation, (i.e. one pick-up roll and one applicator roll).
• the coating was applied to the flat tube surface in reverse roll coating mode.
• the applicator roll was adjusted to give the desired dry film thickness of coating (25 to 28 ⁇ m) and a batch of tubes was coated and the wet coating dried. Thereafter, the tubes were coated on their reverse side and the wet film dried once more so that each flat face of the tube received an equivalent coating thickness.
• a coated tube sample was weighed and then placed in a laboratory muffle furnace at 350°C for 10 minutes. The tube was then carefully removed so as not to disturb the remaining coating and, when cool, was reweighed. The remaining coating was then physically removed by wiping with paper tissue and the tube was then reweighed. From the weight differences the coating thickness could be defined and hence the amount of flux.
• the resulting braze joints showed excellent fillet formation and no free Si-particles were present in the brazed joints.

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• Engineering & Computer Science (AREA)
• Mechanical Engineering (AREA)
• Chemical & Material Sciences (AREA)
• Inorganic Chemistry (AREA)
• Application Of Or Painting With Fluid Materials (AREA)
• Paints Or Removers (AREA)

Priority Applications (9)

Applications Claiming Priority (1)

Related Child Applications (1)

Publications (1)

Family

ID=8167512

Family Applications (1)

Country Status (8)

Cited By (9)

Families Citing this family (8)

Citations (6)

• 1999
  • 1999-11-23 EP EP99959343A patent/EP1232040A1/en not_active Withdrawn
  • 1999-11-23 JP JP2001539635A patent/JP2003514671A/ja not_active Withdrawn
  • 1999-11-23 CN CN99817017A patent/CN1398212A/zh active Pending
  • 1999-11-23 PL PL99355680A patent/PL355680A1/xx unknown
  • 1999-11-23 AU AU16553/00A patent/AU1655300A/en not_active Abandoned
  • 1999-11-23 CZ CZ20021797A patent/CZ20021797A3/cs unknown
  • 1999-11-23 KR KR1020027006510A patent/KR20020058030A/ko not_active Application Discontinuation
  • 1999-11-23 WO PCT/EP1999/009162 patent/WO2001038040A1/en not_active Application Discontinuation

Patent Citations (6)

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