WO2019238347A1 - Method for coating a substrate - Google Patents
Method for coating a substrate Download PDFInfo
- Publication number
- WO2019238347A1 WO2019238347A1 PCT/EP2019/062466 EP2019062466W WO2019238347A1 WO 2019238347 A1 WO2019238347 A1 WO 2019238347A1 EP 2019062466 W EP2019062466 W EP 2019062466W WO 2019238347 A1 WO2019238347 A1 WO 2019238347A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- sol
- gel layer
- substrate
- particles
- coating
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Ceased
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C18/00—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating
- C23C18/02—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating by thermal decomposition
- C23C18/12—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating by thermal decomposition characterised by the deposition of inorganic material other than metallic material
- C23C18/1204—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating by thermal decomposition characterised by the deposition of inorganic material other than metallic material inorganic material, e.g. non-oxide and non-metallic such as sulfides, nitrides based compounds
- C23C18/1208—Oxides, e.g. ceramics
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D5/00—Processes for applying liquids or other fluent materials to surfaces to obtain special surface effects, finishes or structures
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D3/00—Pretreatment of surfaces to which liquids or other fluent materials are to be applied; After-treatment of applied coatings, e.g. intermediate treating of an applied coating preparatory to subsequent applications of liquids or other fluent materials
- B05D3/14—Pretreatment of surfaces to which liquids or other fluent materials are to be applied; After-treatment of applied coatings, e.g. intermediate treating of an applied coating preparatory to subsequent applications of liquids or other fluent materials by electrical means
- B05D3/141—Plasma treatment
- B05D3/145—After-treatment
- B05D3/147—Curing
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D5/00—Processes for applying liquids or other fluent materials to surfaces to obtain special surface effects, finishes or structures
- B05D5/08—Processes for applying liquids or other fluent materials to surfaces to obtain special surface effects, finishes or structures to obtain an anti-friction or anti-adhesive surface
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C18/00—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating
- C23C18/02—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating by thermal decomposition
- C23C18/08—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating by thermal decomposition characterised by the deposition of metallic material
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C18/00—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating
- C23C18/02—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating by thermal decomposition
- C23C18/12—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating by thermal decomposition characterised by the deposition of inorganic material other than metallic material
- C23C18/1204—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating by thermal decomposition characterised by the deposition of inorganic material other than metallic material inorganic material, e.g. non-oxide and non-metallic such as sulfides, nitrides based compounds
- C23C18/1208—Oxides, e.g. ceramics
- C23C18/1216—Metal oxides
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C18/00—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating
- C23C18/02—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating by thermal decomposition
- C23C18/12—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating by thermal decomposition characterised by the deposition of inorganic material other than metallic material
- C23C18/1225—Deposition of multilayers of inorganic material
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C18/00—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating
- C23C18/02—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating by thermal decomposition
- C23C18/12—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating by thermal decomposition characterised by the deposition of inorganic material other than metallic material
- C23C18/125—Process of deposition of the inorganic material
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C18/00—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating
- C23C18/02—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating by thermal decomposition
- C23C18/12—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating by thermal decomposition characterised by the deposition of inorganic material other than metallic material
- C23C18/125—Process of deposition of the inorganic material
- C23C18/1254—Sol or sol-gel processing
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C18/00—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating
- C23C18/14—Decomposition by irradiation, e.g. photolysis, particle radiation or by mixed irradiation sources
- C23C18/145—Radiation by charged particles, e.g. electron beams or ion irradiation
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C28/00—Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C28/00—Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D
- C23C28/40—Coatings including alternating layers following a pattern, a periodic or defined repetition
- C23C28/42—Coatings including alternating layers following a pattern, a periodic or defined repetition characterized by the composition of the alternating layers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D1/00—Processes for applying liquids or other fluent materials
- B05D1/02—Processes for applying liquids or other fluent materials performed by spraying
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D1/00—Processes for applying liquids or other fluent materials
- B05D1/18—Processes for applying liquids or other fluent materials performed by dipping
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D2601/00—Inorganic fillers
- B05D2601/20—Inorganic fillers used for non-pigmentation effect
- B05D2601/24—Titanium dioxide, e.g. rutile
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D2601/00—Inorganic fillers
- B05D2601/20—Inorganic fillers used for non-pigmentation effect
- B05D2601/28—Metals
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D7/00—Processes, other than flocking, specially adapted for applying liquids or other fluent materials to particular surfaces or for applying particular liquids or other fluent materials
- B05D7/50—Multilayers
- B05D7/52—Two layers
- B05D7/54—No clear coat specified
- B05D7/546—No clear coat specified each layer being cured, at least partially, separately
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D7/00—Processes, other than flocking, specially adapted for applying liquids or other fluent materials to particular surfaces or for applying particular liquids or other fluent materials
- B05D7/50—Multilayers
- B05D7/56—Three layers or more
- B05D7/58—No clear coat specified
- B05D7/586—No clear coat specified each layer being cured, at least partially, separately
Definitions
- the invention relates to a method for coating a substrate, which comprises the application of a sol-gel layer to the substrate and the curing of the sol-gel layer applied to the substrate, according to the preamble of claim 1.
- Public transport buses, trains, planes
- public transport users were at least six times as likely to get influenza-related respiratory infections.
- rota- / noro-viruses triggers of diarrhea
- bacterial infections with E. coli, Klebsiella r Proteus, Staph.
- Haemoloticus and saprophyticus which cause inflammation of the intestines, ears and bladder, are often transmitted in public transport.
- Hepatitis A viruses and 16% of rotaviruses are transmitted across surfaces. Once transferred, bacteria and viruses - depending on the type - usually survive for several days to years even on dry surfaces. In the end, studies showed that due to the high passenger density, even daily cleaning has no influence on the microbes. Surfaces pretending to be clean are particularly at risk, for example stainless steel has no antibacterial / antiviral effect.
- Claim 1 relates to a method for coating a substrate, which comprises applying a sol-gel layer to the substrate and curing the sol-gel layer applied to the substrate, according to the invention It is provided that the sol-gel layer is provided with particles with an atmospheric plasma jet which is directed onto the substrate and contains the particles before, during or after the application of the sol-gel layer, and after the application of the sol-gel layer. Layer the hardening of the sol-gel layer takes place by irradiation with an atmospheric plasma beam directed onto the sol-gel layer.
- the method according to the invention thus provides for a combination of thick-film and thin-film technologies by means of sol-gel layer application and atmospheric plasma.
- a thick-film system can be realized which can be provided with a high biocide particle density in a wear-resistant, also biocidal matrix and which shows controlled degeneration and corrosion behavior through corrosion inhibitors and reservoir-forming intermediate layers.
- sol-gel layer application uses sol-gel synthesis, inorganic or organic-inorganic (hybrid polymer) coatings can be produced from colloidal dispersions.
- Sol-gel layers are mainly applied to 3D surfaces by dipping or spraying.
- the coating is finished in a conventional manner by curing at elevated temperature thermally and / or under UV radiation photochemically (with the addition of photoinitiators).
- the applied sol-gel layer is cured by means of an atmospheric plasma jet.
- atmospheric pressure plasma the pressure in the plasma corresponds to the surrounding atmospheric pressure, which means that, in contrast to the low / high pressure plasma, no cost-intensive reaction vessel (eg vacuum chamber) is necessary.
- plasmas can through nozzles (plasma jet), dielectric Barrier discharge (DBD), corona discharge, electrostatic filters and ionizers are produced technically, only the first two being significant for the technical production of coatings according to the invention.
- a high-frequency ignition pulse (10 kV) is used to generate an arc and to maintain the voltage at a constant current, through which the working gas flows and is ionized.
- the outlet takes place at the nozzle head as thermal hot gas plasma, which is at ground potential and thus largely retains potential-carrying parts of the plasma stream.
- the internal structure of the plasma nozzle and the excitation voltage and frequency used define the achievable plasma properties such as density or energy. In principle, however, a lower temperature load for the substrate and thus the use of, for example, plastics as a substrate are made possible.
- a very large working distance compared to the prior art up to 120 mm vs. 30 mm
- an enlarged plasma jet diameter up to 55 mm vs. 20 mm
- the atmospheric plasma jet is also used to provide the sol-gel layer with particles with an atmospheric plasma jet directed before, during or after the application of the sol-gel layer.
- the particles are preferably biocidal particles.
- metals have come into focus for the achievement of biocidal effects, although their tendency to form resistance is low.
- silver is predominantly used, which has a wide spectrum of antimicrobial activity for a large part of all nosocomial bacteria, germs, spores, fungi and viruses. Since silver is also very well tolerated by the body in vivo, non-allergenic and therefore optimal for surfaces of Suitable implants and surgical instruments, its large-scale use in the non-clinical area to avoid the development of resistance is increasingly viewed critically or is also restricted by law.
- biocidal particles which contain copper, zinc or tungsten and / or their oxides, metal salts or titanium dioxide are preferably proposed.
- These particles can be supplied as powdered precursor materials in the form of suitable metal compounds to the plasma jet by means of a carrier gas, which subsequently melt in the plasma jet and are accelerated in the molten or pasty state by the volume expansion of the plasma jet and deposited on the substrate to be coated.
- This process can take place before, during or after the application of the sol-gel layer to the substrate, the goal in each case in the production of a primer layer or covering layer for the sol-gel layer, or in the incorporation of the particles into the sol -Gel layer as well as a combination of these measures can exist.
- the invention can also be used more broadly in that the particles are nanoparticles, microparticles or fibers which have the electrical conductivity, thermal conductivity, piezoelectric properties, magnetic properties, optical reflection / transmission / emission properties, optoelectric properties , biological-functional properties or decorative-colored properties of the sol-gel layer either as storage or change.
- the sol-gel layer is applied by means of a sol-gel matrix which already contains quaternary ammonium salts with a biocidal action, for example Q-POSS, in order to further increase the biocidal effectiveness of the coating. It can also be provided that the sol-gel layer application by means of a sol-gel matrix which contains cerium in order to increase the corrosion resistance of the hardened sol-gel layer.
- the sol-gel layer is cured according to the invention by irradiation with an atmospheric plasma jet directed onto the sol-gel layer.
- Curing can be carried out with the same plasma generator with which the sol-gel layer was also provided with particles, only the supply of the precursor material for the introduction of the particles into the plasma beam being prevented.
- the hardening of the sol-gel layer by means of atmospheric plasma jet can be carried out more quickly than with conventional thermal treatment, so that higher layer thicknesses can be achieved, and in particular the production of a multilayer structure of the applied layer is economically possible, in that several sol-gel layers each after Curing can be applied to the substrate one after the other by the atmospheric plasma.
- the atmospheric plasma has also proven to be extremely suitable for curing a sol-gel layer. Due to the high, but briefly acting temperatures of the atmospheric plasma - the core temperature of an atomic plasma is around 5000-10,000 ° C - a sol-gel layer can be cured quickly and without cracks even with thick layers.
- the UV radiation generated in the plasma can also be used for curing, in particular when photoinitiators are present in the sol-gel layer.
- continuous processes can also be realized by moving the substrate from one location of the sol-gel layer application to the plasma head. Simultaneous surface treatment of the substrate with sol-gel layer application and plasma treatment is also conceivable.
- the particles be admixed as a coating material with the atmospheric plasma jet which causes the hardening of the sol-gel layer.
- the coating material can in turn be applied with the same plasma generator, with the plasma jet merely being supplied with a suitable precursor for the desired coating. It is preferably a polymerizable precursor.
- SiO 2, TiO 2, SnO x , CrO x , diamond-like carbon and polymer layers can be produced in a known manner. The process proceeds from the formation of radicals in the gas phase through collision with surrounding particles and the very intense UV radiation in the plasma, which enables polymerization.
- the structure of the plasma polymers is close to that of conventional polymers, especially with low energy input per precursor monomer.
- These precursors can be added in the highly ionized discharge zone or only in the quasi-neutral plasma zone without interaction of electrons and ions.
- a special position is the "atmospheric plas a liquid deposition", where droplets are sprayed into the plasma instead of precursor vapor, which prevents damage to fragile organic molecules by ionization.
- the use of an atmospheric plasma jet according to the invention thus enables curing and surface modification because of the intense (UV) radiation also the production of polymer and oxide ceramic thin layers, whereby the significantly larger working distance gives decisive advantages in the use of 3D objects.
- the (simultaneous) use of precursors for layer deposition is very advantageous for single-step functionalization during curing, i.e. the use of intermediate layers to increase toughness, hardness or wear resistance and as permeation barrier layers to increase corrosion protection by minimizing the Nanoporosity.
- the coating material can also be metallic or ceramic particles.
- a coating of a substrate with a biocidal effect which comprises a hardened sol-gel layer containing copper, zinc, tungsten and / or their oxides, metal salts, or titanium dioxide, and a layer consisting of a polymerized and by means of a atmospheric plasma jet polymerizable precursor is formed.
- the precursor polymerizable by means of an atmospheric plasma jet is preferably HMDSO or TEOS.
- the method according to the invention can be expanded in that a multilayer structure is carried out with the aid of a sequence of sol-gel layer applications and irradiation with the atmospheric plasma jet. Thanks to the multilayer structure, high layer thicknesses can be achieved, which maintain the functionality of the biocidal coating over a long period of time.
- a coating of a substrate with a biocidal effect is proposed, which comprises a hardened sol-gel layer containing copper, zinc, tungsten and / or their oxides, metal salts, or titanium dioxide, and a layer which is formed from metallic or ceramic particles ,
- a substrate with a biocidal effect comprises a hardened sol-gel layer containing copper, zinc, tungsten and / or their oxides, metal salts, or titanium dioxide, and a layer which is formed from metallic or ceramic particles .
- Fig. 1 is a sectional view through a possible embodiment of a plasma generator for curing the sol-gel layer and for supplying the biocidal particles and the
- Fig. 2a is a schematic representation of a possible
- 3a shows a schematic representation of a coating produced by the method according to the invention.
- 3b shows a schematic representation of a multilayer structure produced by the method according to the invention.
- the device comprises a plasma generator 1, which has a cathode 2 and an anode 5.
- the cathode 2 is cylindrical and has at its free end a conical end region 3 which, in the exemplary embodiment shown, projects into an outlet channel 4 for the plasma jet AP.
- the anode 5 is arranged coaxially with the cathode 2, the cathode 2 and the anode 5 being connected to a controllable voltage source 6.
- a direct voltage in the range of 10-30 V at a current of 60-500 A is applied between the cathode 2 and the anode 5.
- the electrical power of the plasma generator moves in the Range of 600-10000 W.
- the inside of the cathode 2 can optionally be provided with cathode cooling (not shown in FIG. 1).
- coolant channels 10 are provided in the jacket body of the plasma generator 1, which are connected to a coolant source 11 and cool the plasma generator 1.
- the cathode 2 and the anode 5 delimit a working gas channel 7, which is connected to a controllable working gas source 8.
- a working gas channel 7 opens into the outlet channel 4, which opens into the surrounding atmosphere via an outflow opening 9.
- a voltage is applied to the cathode 2 and the anode 5 which is selected to be sufficiently high to ignite an arc between the tapering end region of the cathode 2 and the anode 5 surrounding the cathode 2.
- This electrical discharge ionizes the working gas flowing through the working channel 7, which subsequently flows through the outlet channel 4 as a plasma and exits as a plasma jet AP through the outflow opening 9 into the surrounding atmosphere.
- the atmospheric area adjoining the outflow opening 9 is subsequently referred to as the outflow area 14 and is indicated in FIG. 1 with dotted lines.
- the outflow of the plasma jet AP in the surrounding atmosphere depends in particular on the operating pressure of the working gas source 8 and the current applied to the cathode 2 and anode 5.
- a holder 12 is also arranged on the plasma generator 1 at its outflow end, via which a feed device of a corresponding precursor material PP for a first type of particles P to be introduced and the precursor PB for a second type serving as coating material B. particle P to be introduced is attached.
- the feed device comprises two feed tubes 13, each of which is connected on the inlet side to an evaporator 15 for the precursor material PP for a first type of particle P to be introduced and for the precursor PB for a second type of particle P to be used as coating material B, and one on the outlet side Have outlet opening 16 which are directed into the outflow region 14.
- the evaporator 15 is connected to at least one storage container 17 for the precursor PB or for the precursor material PP.
- FIG. 2a shows a schematic representation of a possible embodiment of the method according to the invention as a continuous method, in which the substrate 18 is moved from a place where a sol-gel layer matrix SM is applied to the plasma generator 1. If a multilayer structure is desired, alternating positioning between the location of the application of the sol-gel layer matrix SM and the plasma generator 1 can also be assumed (dashed arrow in FIG. 2a).
- 2b shows a schematic representation of a further possible embodiment of the method according to the invention, in which a simultaneous surface treatment of the substrate 18 is carried out by applying a sol-gel layer matrix SM and plasma treatment.
- a sol-gel layer matrix SM is applied to the substrate 18, in the exemplary embodiment shown in FIG. 2, for example using a spraying method.
- Methods for applying a sol-gel layer matrix SM to a substrate 18 are well known.
- sol or gel synthesis can be used to produce inorganic or organically inorganic (hybrid polymer) coatings from colloidal dispersions, chemical process engineering first requiring a hydrolysis reaction of the alcoholate precursor (Formation of “sol particles”). These are condensed catalytically into chains by adding acid or base.
- Precursor molecules are often based on silicon (TEOS, TMOS), titanium or zirconium compounds, with the incorporation of appropriate organo-functional silicon compounds in the inorganic network in the condensation, the properties of the resulting sol-gel layers S can be set in a targeted manner.
- Possibilities include making the network more flexible, setting the curing conditions, forming an additional organic network (in addition to the inorganic), varying the surface energy, or increasing the Scratch resistance through co-condensation with metal alkoxides such as aluminum alkoxide
- All essential basic reactions, ie hydrolysis and the subsequent condensation reaction between the resulting reactive species to form the 3D network are dynamic processes of many interlocking equilibrium reactions and can be controlled via pH, temperature or precursor molecule concentrations.
- sol-gel layers S can also be applied to 3D surfaces by immersion processes or spin coating.
- the sol-gel layer application can be carried out by means of a sol-gel layer matrix SM which already contains biocidal substances, for example quaternary ammonium salts with a biocidal effect, in particular Q-POSS. Provision can also be made for the sol-gel layer to be applied by means of a sol-gel layer matrix SM which contains cerium in order to increase the corrosion resistance of the hardened sol-gel layer S.
- a sol-gel layer matrix SM which already contains biocidal substances, for example quaternary ammonium salts with a biocidal effect, in particular Q-POSS.
- Metallic materials but also plastics, in particular thermoplastics, can be used as substrate 18, since due to the indirectly transmitted arc in the subsequent plasma treatment, both electrically conductive and non-conductive substrates such as glass-like materials, composite materials (CFRP / GFRP) or plastics can be coated.
- electrically conductive and non-conductive substrates such as glass-like materials, composite materials (CFRP / GFRP) or plastics can be coated.
- the substrate 18 is exposed to the plasma jet AP of a plasma generator 1 after the sol-gel layer S has been applied, in order to introduce particles P of a first type, for example biocidal particles, into the sol-gel layer S. If the sol-gel layer S already contains biocidal substances, this step can also be omitted.
- the particles P are added in the form of a corresponding precursor material PP to the evaporator 15 and subsequently to the plasma jet AP by means of a carrier gas and applied in the form of the particles P to the substrate 18, where they are embedded in the sol-gel layer S.
- biocidal particles P which contain copper, zinc or tungsten and / or their oxides or titanium dioxide are preferably proposed.
- 2b shows a schematic representation of a further possible embodiment of the method according to the invention, in which a simultaneous surface treatment of the substrate 18 is carried out by applying a sol-gel layer S and introducing the particles P through the atmospheric plasma AP.
- the sol-gel layer S is cured according to the invention by irradiation with an atmospheric plasma jet AP directed onto the sol-gel layer S.
- Particles P of a second type serving as coating material B can be admixed with the atmospheric plasma jet AP causing the hardening of the sol-gel layer S.
- This coating material B can in turn be applied with the same plasma generator 1, the plasma jet AP merely having a suitable precursor PB for the desired coating is fed. It is preferably a polymerizable precursor PB.
- These precursors PB preferably HMDSO or TEOS, can be added to the plasma jet AP in the highly ionized discharge zone or only in the zone of quasi-neutral plasma without interaction of electrons and ions.
- an atmospheric plasma jet AP thus enables not only curing and surface modification due to the intense (UV) radiation, but also the production of polymer and oxide-ceramic thin layers, the decisive advantage being achieved in the use of 3D objects due to the significantly larger working distance.
- the hardening of the sol-gel layer by means of atmospheric plasma jet AP can be carried out more quickly than with conventional thermal treatment, so that higher layer thicknesses can be achieved, and in particular a multilayer structure of the applied layer is economically possible by using several sol-gel layers S each Curing by the atmospheric plasma AP can be applied successively to the substrate 18, as will be explained with reference to FIG. 3.
- FIG. 3a shows a schematic illustration of a coating produced by the method according to the invention, comprising a sol-gel layer S and a layer of a coating material B
- FIG. 3b shows a schematic illustration of a multilayer structure comprising two sol- Gel layers S and two layers of a coating material B.
- Biocidal particles P are embedded in the sol-gel layer S, for example in the form of biocidal metal (oxide) particles.
- the sol-gel layer S can contain biocidal quaternary ammonium salts in order to further increase the biocidal effectiveness of the coating. It can also be provided that the sol-gel layer S contains cerium-based corrosion inhibitors to increase the corrosion resistance of the hardened sol-gel layer S.
- 3a and 3b comprises a layer of a coating material B which, in the exemplary embodiment shown, is formed from a polymerized precursor PB which can be polymerized by means of an atmospheric plasma jet AP.
- the precursor PB polymerizable by means of an atmospheric plasma jet AP is, for example, HMDSO or TEOS.
- This layer can be referred to as a permeation barrier layer since it represents a spatial delimitation of the biocidal reservoir given by the particles P of the sol-gel layer S.
- the multilayer structure shown in FIG. 3 enables high layer thicknesses to be achieved which maintain the functionality of the biocidal coating over a long period of time.
- the subject invention thus enables a process for producing durable, hard, corrosion, abrasion and wear resistant coatings with a biocidal effect, which is also economically applicable.
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- General Chemical & Material Sciences (AREA)
- Thermal Sciences (AREA)
- Inorganic Chemistry (AREA)
- Ceramic Engineering (AREA)
- Toxicology (AREA)
- Dispersion Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Plasma & Fusion (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Laminated Bodies (AREA)
Abstract
Description
Verfahren zur Beschichtung eines Substrats Process for coating a substrate
Die Erfindung betrifft ein Verfahren zur Beschichtung eines Substrats, das das Aufträgen einer Sol-Gel-Schicht auf das Substrat sowie das Aushärten der auf das Substrat aufgetragenen Sol-Gel-Schicht umfasst, gemäß dem Oberbegriff von Anspruch 1. The invention relates to a method for coating a substrate, which comprises the application of a sol-gel layer to the substrate and the curing of the sol-gel layer applied to the substrate, according to the preamble of claim 1.
Öffentliche Verkehrsmittel (Busse, Bahnen, Flugzeuge) sind durch den engen Kontakt der Fahrgäste Hauptübertragungsorte für Bakterien und Viren. Studien zeigten für Nutzer öffentlicher Verkehrsmittel ein mindestens sechsmal so hohes Risiko, an grippalen Atemwegs-Infekten zu erkranken. Neben Rhinoviren übertragen sich auch Rota-/Noro-Viren (Auslöser von Diarrhoe) vornehmlich in dichten Menschenansammlungen. Neben viralen werden vielfach auch bakterielle Infektionen mit E. coli , Klebsiella r Proteus, Staph. haemoloticus und saprophyticus, welche zu Darm-, Ohren- und Blasenentzündungen führen, häufig in öffentlichen Verkehrsmitteln übertragen. Dies führte ausgehend von Flugzeugen zu einem verbreiteten Einsatz von HEPA-Filtern in Klimaanlagen und Umluft-Systemen, was das Tröpfcheninfektionsrisiko deutlich minimieren konnte, aber eine Verschiebung hin zu Schmierinfektion über die Hände und anschließenden Transport zu den Schleimhäuten aufzeigte. Bakterien und Viren sind vor allem auf Sitzen, Handgriffen, Tastern/Schaltern, Braille-Blindenschrift-Schildern und Klapptischen zu finden, wobei vermehrt auch nosokomiale Antibiotika-resistente Staphylokokken-Typen aufgefunden werden. Der Transfer ist dabei über harte, nicht-poröse Oberflächen am effizientesten, wobei bis zu 60% aller Personen durch fehlenden Zugang zu Handhygiene während der „Reise" hohe Dichten an Fäkalbakterien auf ihren Händen haben. Detaillierte Studien zum Transfer verschiedener Pathogene (d.h. krankheitsauslösende Bakterien, Viren, Sporen) zeigen, dass über den Handkontakt 100% von E. coli, Salmonella spp Staph. Aureus, 90% von C. albicans, 61% der Rhinoviren, 22-33% derPublic transport (buses, trains, planes) are the main transmission points for bacteria and viruses due to the close contact between passengers. Studies showed that public transport users were at least six times as likely to get influenza-related respiratory infections. In addition to rhinoviruses, rota- / noro-viruses (triggers of diarrhea) are mainly transmitted in crowds of people. In addition to viral infections, bacterial infections with E. coli, Klebsiella r Proteus, Staph. Haemoloticus and saprophyticus, which cause inflammation of the intestines, ears and bladder, are often transmitted in public transport. Based on aircraft, this led to widespread use of HEPA filters in air conditioning and circulating air systems, which was able to significantly minimize the risk of droplet infection, but showed a shift towards smear infection via the hands and subsequent transport to the mucous membranes. Bacteria and viruses are mainly found on seats, handles, buttons / switches, braille braille signs and folding tables, although nosocomial antibiotic-resistant staphylococcal types are also increasingly being found. The transfer is most efficient over hard, non-porous surfaces, whereby up to 60% of all people have high densities of faecal bacteria on their hands due to the lack of access to hand hygiene during the "journey". Detailed studies on the transfer of various pathogens (ie disease-causing bacteria , Viruses, spores) show that 100% of E. coli, Salmonella spp Staph. Aureus, 90% of C. albicans, 61% of the rhinoviruses, 22-33% of the
Hepatitis A Viren und 16% der Rotaviren über Oberflächen übertragen werden. Einmal transferierte Bakterien und Viren überleben - abhängig vom Typ - sogar auf trockenen Oberflächen meist mehrere Tage bis Jahre. Schlussendlich zeigten Studien, dass durch die hohe Fahrgastdichte auch eine tägliche Reinigung keinen Einfluss auf die Mikroben hat. Sauberkeit vortäuschende Flächen sind besonders gefährdet, so hat etwa Edelstahl keine antibakterielle/antivirale Wirkung. Hepatitis A viruses and 16% of rotaviruses are transmitted across surfaces. Once transferred, bacteria and viruses - depending on the type - usually survive for several days to years even on dry surfaces. In the end, studies showed that due to the high passenger density, even daily cleaning has no influence on the microbes. Surfaces pretending to be clean are particularly at risk, for example stainless steel has no antibacterial / antiviral effect.
Daher wurde die Anfertigung von antibakteriellen Oberflächen versucht. So wurde beispielsweise photokatalytisch wirkendes Ti02 in organischen Lacken integriert, wobei speziell die Lebensdauer durch die abrasive Beanspruchung sehr begrenzt ist. Inorganische Vakuum-Beschichtungen wären deutlich verschleißfester, sind aber für große Flächen technisch schwierig und zu kostenintensiv. Eine weitere Alternative stellt die „Vernickelung" (Ni-Sn-Matrix mit Ti02-Partikel ) dar, welche jedoch für Nickel-Allergiker problematisch ist und zudem nachträglich nicht mehr ohne Demontage aufgebracht werden kann. Letzteres ist durch die lange Nutzungsdauer (bis zu 35 Jahren) besonders wichtig, um auch vorhandene Verkehrsmittel nachträglich ausstatten zu können. Therefore, the creation of antibacterial surfaces was tried. For example, Ti02 with a photocatalytic effect has been integrated into organic coatings, with the service life being very limited due to the abrasive stress. Inorganic vacuum coatings would be significantly more wear-resistant, but are technically difficult and too expensive for large areas. Another alternative is the "nickel plating" (Ni-Sn matrix with Ti02 particles), which is problematic for nickel allergy sufferers and, moreover, can no longer be applied without disassembly. The latter is due to the long service life (up to 35 Years) is particularly important in order to be able to retrofit existing means of transport.
Es besteht somit das Ziel der Erfindung darin ein Verfahren zur dauerhaften, harten, Korrosions-, Abrieb- und Verschleißbeständigen Beschichtung eines Substrats mit biozider Wirkung bereitzustellen, das zudem auch nachträglich und wiederholt wirtschaftlich einsetzbar ist. It is therefore the aim of the invention to provide a process for the permanent, hard, corrosion, abrasion and wear-resistant coating of a substrate with a biocidal effect, which is also subsequently and repeatedly economically usable.
Dieses Ziel wird durch die Merkmale von Anspruch 1 erreicht. Anspruch 1 bezieht sich auf ein Verfahren zur Beschichtung eines Substrats, das das Aufträgen einer Sol-Gel-Schicht auf das Substrat sowie das Aushärten der auf das Substrat aufgetragenen Sol-Gel-Schicht umfasst, wobei erfindungsgemäß vorgesehen ist, dass die Sol-Gel-Schicht mit Partikel mit einem vor, während oder nach dem Aufträgen der Sol-Gel-Schicht auf das Substrat gerichteten und die Partikel enthaltenden, atmosphärischen Plasmastrahl versehen wird, und nach dem Aufträgen der Sol-Gel-Schicht die Aushärtung der Sol-Gel- Schicht durch Bestrahlung mit einem auf die Sol-Gel-Schicht gerichteten, atmosphärischen Plasmastrahl erfolgt. Das erfindungsgemäße Verfahren sieht somit eine Kombination von Dickschicht- und Dünnschicht-Technologien mittels Sol-Gel- Schichtauftrag und atmosphärischem Plasma vor. Wie noch näher beschrieben werden wird, kann auf diese Weise ein Dickschichtsystem verwirklicht werden, das mit einer hohen Biozid-Partikeldichte in einer verschleißfesten, ebenfalls bioziden Matrix versehen werden kann und durch Korrosionsinhibitoren und Reservoir-bildenden Zwischenschichten ein kontrolliertes Degenerations- und Korrosionsverhalten zeigt. This goal is achieved by the features of claim 1. Claim 1 relates to a method for coating a substrate, which comprises applying a sol-gel layer to the substrate and curing the sol-gel layer applied to the substrate, according to the invention It is provided that the sol-gel layer is provided with particles with an atmospheric plasma jet which is directed onto the substrate and contains the particles before, during or after the application of the sol-gel layer, and after the application of the sol-gel layer. Layer the hardening of the sol-gel layer takes place by irradiation with an atmospheric plasma beam directed onto the sol-gel layer. The method according to the invention thus provides for a combination of thick-film and thin-film technologies by means of sol-gel layer application and atmospheric plasma. In this way, as will be described in more detail, a thick-film system can be realized which can be provided with a high biocide particle density in a wear-resistant, also biocidal matrix and which shows controlled degeneration and corrosion behavior through corrosion inhibitors and reservoir-forming intermediate layers.
Techniken für den Sol-Gel-Schichtauftrag sind hinlänglich bekannt. Mittels der Sol-Gel-Synthese können aus kolloidalen Dispersionen anorganische oder organisch-anorganische (hybridpolymere) Beschichtungen hergestellt werden. Sol-Gel-Schichten werden überwiegend durch Tauch-oder Sprühverfahren auf 3D- Oberflächen aufgebracht. Die Beschichtung wird in herkömmlicher Weise durch eine Aushärtung bei erhöhter Temperatur thermisch und/oder unter UV-Strahlung photochemisch (bei Zugabe von Photoinitiatoren) abgeschlossen. Techniques for sol-gel layer application are well known. Using sol-gel synthesis, inorganic or organic-inorganic (hybrid polymer) coatings can be produced from colloidal dispersions. Sol-gel layers are mainly applied to 3D surfaces by dipping or spraying. The coating is finished in a conventional manner by curing at elevated temperature thermally and / or under UV radiation photochemically (with the addition of photoinitiators).
Erfindungsgemäß ist eine Aushärtung der aufgetragenen Sol-Gel- Schicht hingegen durch einen atmosphärischen Plasmastrahl vorgesehen. Beim Atmosphärendruck-Plasma entspricht der Druck im Plasma dem umgebenden Atmosphärendruck, wodurch im Gegensatz zum Nieder-/Hochdruckplasma kein kostenintensives Reaktionsgefäß (z.B. Vakuumkammer) notwendig ist. Derartige Plasmen können durch Düsen (Plasma-Jet) , dielektrische Barriereentladung (DBD) , Koronaentladung, Elektrofilter und Ionisatoren technisch erzeugt werden, wobei für die technische Herstellung von erfindungsgemäßen Beschichtungen nur die ersten beiden bedeutend sind. Bei Plasmadüsen wird mittels eines Hochfrequenz-Zündimpulses (10 kV) ein Lichtbogen erzeugt und bei konstantem Strom spannungsgeregelt aufrecht erhalten, durch den das Arbeitsgas strömt und ionisiert wird. Der Austritt erfolgt am Düsenkopf als thermisches Heißgasplasma, welcher auf Massepotential liegt und damit potentialführende Teile des Plasmastromes weitgehend zurückhält. Der innere Aufbau der Plasmadüse sowie die genutzte Anregungsspannung und -frequenz definieren die erzielbaren Plasmaeigenschaften wie Dichte oder Energie. Grundsätzlich werden aber eine geringere Temperaturbelastung für das Substrat und damit die Verwendung von z.B. Kunststoffen als Substrat ermöglicht. Alternativ kann durch entsprechende Elektroden- und Düsenform und Gasflüsse ein gegenüber dem Stand der Technik sehr großer Arbeitsabstand (bis 120 mm vs . 30 mm) bei vergrößertem Plasmastrahl- Durchmesser (bis 55 mm vs . 20 mm) genutzt werden, was eine wirtschaftliche Anwendbarkeit des erfindungsgemäßen Verfahrens für 3D-Oberflächen ermöglicht. According to the invention, however, the applied sol-gel layer is cured by means of an atmospheric plasma jet. In the case of atmospheric pressure plasma, the pressure in the plasma corresponds to the surrounding atmospheric pressure, which means that, in contrast to the low / high pressure plasma, no cost-intensive reaction vessel (eg vacuum chamber) is necessary. Such plasmas can through nozzles (plasma jet), dielectric Barrier discharge (DBD), corona discharge, electrostatic filters and ionizers are produced technically, only the first two being significant for the technical production of coatings according to the invention. In the case of plasma nozzles, a high-frequency ignition pulse (10 kV) is used to generate an arc and to maintain the voltage at a constant current, through which the working gas flows and is ionized. The outlet takes place at the nozzle head as thermal hot gas plasma, which is at ground potential and thus largely retains potential-carrying parts of the plasma stream. The internal structure of the plasma nozzle and the excitation voltage and frequency used define the achievable plasma properties such as density or energy. In principle, however, a lower temperature load for the substrate and thus the use of, for example, plastics as a substrate are made possible. Alternatively, by means of appropriate electrode and nozzle shape and gas flows, a very large working distance compared to the prior art (up to 120 mm vs. 30 mm) with an enlarged plasma jet diameter (up to 55 mm vs. 20 mm) can be used, which makes the Allows the inventive method for 3D surfaces.
Erfindungsgemäß wird der atmosphärische Plasmastrahl auch dazu verwendet, die Sol-Gel-Schicht mit Partikel mit einem vor, während oder nach dem Aufträgen der Sol-Gel-Schicht auf das Substrat gerichteten, atmosphärischen Plasmastrahl zu versehen. Bei den Partikeln handelt es sich vorzugsweise um biozide Partikel. Für die Erzielung biozider Wirkung gelangten in jüngerer Vergangenheit Metalle in den Blickpunkt, wobei deren Neigung zur Resistenzbildung gering ist. Derzeit wird überwiegend Silber verwendet, das ein weites Spektrum an antimikrobieller Aktivität für einen Großteil aller nosokomialer Bakterien, Keime, Sporen, Pilze und Viren besitzt. Da Silber auch sehr gut in vivo körperverträglich, nicht-allergen und damit optimal für Oberflächen von Implantaten und chirurgischen Instrumenten geeignet ist, wird dessen großflächiger Einsatz im nichtklinischen Bereich zur Vermeidung der Resistenzbildung jedoch zunehmend kritisch betrachtet bzw. darüber hinaus gesetzlich beschränkt. Im Rahmen der vorliegenden Erfindung werden daher vorzugsweise biozide Partikel, die Kupfer, Zink oder Wolfram und/oder deren Oxide, Metallsalze, oder Titandioxid enthalten, vorgeschlagen. Diese Partikel können als pulverförmige Precursormaterialien in Form geeigneter Metallverbindungen dem Plasmastrahl mittels eines Trägergases zugeführt werden, die in weiterer Folge im Plasmastrahl aufschmelzen und im schmelzflüssigen oder teigigen Zustand durch die Volumensexpansion des Plasmastrahls beschleunigt und auf das zu beschichtende Substrat abgeschieden werden. Dieser Vorgang kann vor, während oder nach dem Aufträgen der Sol-Gel-Schicht auf das Substrat erfolgen, wobei das Ziel jeweils in der Herstellung einer Grundierungsschicht oder bedeckenden Schicht für die Sol-Gel- Schicht, oder in der Einlagerung der Partikel in die Sol-Gel- Schicht sowie einer Kombination dieser Maßnahmen bestehen kann. Dabei kann die Erfindung auch breiter eingesetzt werden, indem es sich bei den Partikeln um Nanopartikel , Mikropartikel oder Fasern handelt, die die elektrische Leitfähigkeit, thermische Leitfähigkeit, piezoelektrischen Eigenschaften, magnetischen Eigenschaften, optischen Reflexions- /Transmissions-/Emissions-Eigenschaften, optoelektrischen Eigenschaften, biologisch-funktionellen Eigenschaften oder dekorativ-farblichen Eigenschaften der Sol-Gel-Schicht entweder als Ein- oder Anlagerung verändern. According to the invention, the atmospheric plasma jet is also used to provide the sol-gel layer with particles with an atmospheric plasma jet directed before, during or after the application of the sol-gel layer. The particles are preferably biocidal particles. In the recent past, metals have come into focus for the achievement of biocidal effects, although their tendency to form resistance is low. Currently silver is predominantly used, which has a wide spectrum of antimicrobial activity for a large part of all nosocomial bacteria, germs, spores, fungi and viruses. Since silver is also very well tolerated by the body in vivo, non-allergenic and therefore optimal for surfaces of Suitable implants and surgical instruments, its large-scale use in the non-clinical area to avoid the development of resistance is increasingly viewed critically or is also restricted by law. In the context of the present invention, therefore, biocidal particles which contain copper, zinc or tungsten and / or their oxides, metal salts or titanium dioxide are preferably proposed. These particles can be supplied as powdered precursor materials in the form of suitable metal compounds to the plasma jet by means of a carrier gas, which subsequently melt in the plasma jet and are accelerated in the molten or pasty state by the volume expansion of the plasma jet and deposited on the substrate to be coated. This process can take place before, during or after the application of the sol-gel layer to the substrate, the goal in each case in the production of a primer layer or covering layer for the sol-gel layer, or in the incorporation of the particles into the sol -Gel layer as well as a combination of these measures can exist. The invention can also be used more broadly in that the particles are nanoparticles, microparticles or fibers which have the electrical conductivity, thermal conductivity, piezoelectric properties, magnetic properties, optical reflection / transmission / emission properties, optoelectric properties , biological-functional properties or decorative-colored properties of the sol-gel layer either as storage or change.
Gemäß einer Ausführungsform der Erfindung erfolgt der Sol-Gel- Schichtauftrag mittels einer Sol-Gel-Matrix, die bereits biozid wirkende quaternäre Ammoniumsalze enthält, beispielsweise Q-POSS, um die biozide Wirksamkeit der Beschichtung noch zu erhöhen. Zudem kann vorgesehen sein, dass der Sol-Gel-Schichtauftrag mittels einer Sol-Gel-Matrix erfolgt, die Cer enthält, um die Korrosionsbeständigkeit der ausgehärteten Sol-Gel-Schicht zu erhöhen. According to one embodiment of the invention, the sol-gel layer is applied by means of a sol-gel matrix which already contains quaternary ammonium salts with a biocidal action, for example Q-POSS, in order to further increase the biocidal effectiveness of the coating. It can also be provided that the sol-gel layer application by means of a sol-gel matrix which contains cerium in order to increase the corrosion resistance of the hardened sol-gel layer.
Nach dem Aufträgen der mit bioziden Eigenschaften ausgestatteten Sol-Gel-Schicht erfolgt erfindungsgemäß die Aushärtung der Sol-Gel-Schicht durch Bestrahlung mit einem auf die Sol-Gel-Schicht gerichteten, atmosphärischen Plasmastrahl. Die Aushärtung kann mit demselben Plasmaerzeuger erfolgen, mit dem auch die Sol-Gel-Schicht mit Partikel versehen wurde, wobei lediglich die Zufuhr des Precursormaterials für die Einbringung der Partikel in den Plasmastrahl unterbunden wird. Die Aushärtung der Sol-Gel-Schicht mittels atmosphärischem Plasmastrahl kann rascher erfolgen als mit herkömmlicher thermischer Behandlung, sodass höhere Schichtdicken verwirklicht werden können, und insbesondere auch die Herstellung eines Mehrlagenaufbaus der aufgebrachten Schicht wirtschaftlich möglich ist, indem mehrere Sol-Gel-Schichten jeweils nach Aushärtung durch das atmosphärische Plasma nacheinander auf das Substrat aufgebracht werden. Das atmosphärische Plasma hat sich auch als überaus geeignet für die Aushärtung einer Sol-Gel-Schicht erwiesen. Aufgrund der hohen, aber kurz einwirkenden Temperaturen des atmosphärischen Plasmas - die Kerntemperatur eines atomsphärischen Plasmas beträgt etwa 5000-10.000 °C - kann eine Sol-Gel-Schicht auch bei hohen Schichtdicken rasch und rissfrei ausgehärtet werden. Zudem kann auch die im Plasma erzeugte UV-Strahlung für die Aushärtung genutzt werden, insbesondere bei Präsenz von Photoinitiatoren in der Sol-Gel-Schicht. Durch die erfindungsgemäße Anwendung von Atmosphärendruck-Prozessen, nämlich des Sol-Gel-Schichtaufträges und der Atmosphären- Plasmabehandlung, können auch kontinuierliche Verfahren verwirklicht werden, indem das Substrat von einem Ort des Sol- Gel-Schichtaufträges zum Plasmakopf bewegt wird. Auch eine gleichzeitige Oberflächenbehandlung des Substrats mit Sol-Gel- Schichtauftrag und Plasmabehandlung ist denkbar. Zudem ist es auch denkbar, bloß ausgewählte Teilbereiche der aufgetragenen Sol-Gel-Schicht mit dem atmosphärischen Plasma zu härten und die verbleibenden Bereiche der Sol-Gel-Schicht wieder zu entfernen, um somit nur ausgewählte Teilbereiche des Substrats zu beschichten. Durch die erfindungsgemäße Anwendung von Atmosphärendruck-Prozessen ist außerdem eine wirtschaftliche Realisierbarkeit gewährleistet. After application of the sol-gel layer provided with biocidal properties, the sol-gel layer is cured according to the invention by irradiation with an atmospheric plasma jet directed onto the sol-gel layer. Curing can be carried out with the same plasma generator with which the sol-gel layer was also provided with particles, only the supply of the precursor material for the introduction of the particles into the plasma beam being prevented. The hardening of the sol-gel layer by means of atmospheric plasma jet can be carried out more quickly than with conventional thermal treatment, so that higher layer thicknesses can be achieved, and in particular the production of a multilayer structure of the applied layer is economically possible, in that several sol-gel layers each after Curing can be applied to the substrate one after the other by the atmospheric plasma. The atmospheric plasma has also proven to be extremely suitable for curing a sol-gel layer. Due to the high, but briefly acting temperatures of the atmospheric plasma - the core temperature of an atomic plasma is around 5000-10,000 ° C - a sol-gel layer can be cured quickly and without cracks even with thick layers. In addition, the UV radiation generated in the plasma can also be used for curing, in particular when photoinitiators are present in the sol-gel layer. Through the use of atmospheric pressure processes according to the invention, namely the sol-gel layer application and the atmospheric plasma treatment, continuous processes can also be realized by moving the substrate from one location of the sol-gel layer application to the plasma head. Simultaneous surface treatment of the substrate with sol-gel layer application and plasma treatment is also conceivable. It is also it is also conceivable to cure only selected partial areas of the applied sol-gel layer with the atmospheric plasma and to remove the remaining areas of the sol-gel layer in order to coat only selected partial areas of the substrate. The use of atmospheric pressure processes according to the invention also ensures economic feasibility.
Vorzugsweise wird zudem vorgeschlagen, dass die Partikel dem die Aushärtung der Sol-Gel-Schicht bewirkenden, atmosphärischen Plasmastrahl als Beschichtungsmaterial beigemengt werden. Der Auftrag des Beschichtungsmaterials kann wiederum mit demselben Plasmaerzeuger erfolgen, wobei dem Plasmastrahl lediglich ein geeigneter Precursor für die gewünschte Beschichtung zugeführt wird. Vorzugsweise handelt es dabei um einen polymerisierbaren Precursor. Mittels Plasmapoly erisations-Prozessen unter Atmosphärendruck können etwa in bekannter Weise Si02-, Ti02-, SnOx-, CrOx-, diamantähnliche Kohlenstoff- und Polymer-Schichten hergestellt werden. Der Prozess läuft dabei ausgehend von der Bildung von Radikalen in der Gasphase durch Kollision mit umgebenden Partikeln und die sehr intensive UV-Strahlung im Plasma ab, wodurch Polymerisation ermöglicht wird. Die Struktur der Plasmapolymere ist vor allem bei niedriger Energiezufuhr je Precursor-Monomer nahe jener von konventionellen Polymeren. Die Zugabe dieser Precursoren (z.B. HMDSO, TEOS, TiC14, C2H2, etc.) kann in der hochionisierten Entladungszone oder erst in der Zone von quasineutralem Plasma ohne Wechselwirkung von Elektronen und Ionen erfolgen. Eine Sonderstellung stellt die „atmospheric plas a liquid deposition" dar, wo Tröpfchen anstatt Precursor-Dampf in das Plasma eingesprüht werden, wodurch die Schädigung von fragilen organischen Molekülen durch Ionisation verhindert wird. Die erfindungsgemäße Verwendung eines atmosphärischen Plasmastrahls ermöglicht somit neben der Aushärtung und Oberflächenmodifikation aufgrund der intensiven (UV- ) Strahlung auch die Herstellung von Polymer- und oxidkeramischen Dünnschichten, wobei durch den deutlich größeren Arbeitsabstand entscheidende Vorteile in der Anwendung an 3D-Objekten erzielt werden. Die (gleichzeitige) Nutzung von Precursoren zur Schichtabscheidung ist dabei sehr vorteilhaft für eine Single-Step-Funktionalisierung während der Aushärtung, d.h. der Nutzung von Zwischenschichten zur Zähigkeits-, Härte oder Verschleißfestigkeits-Erhöhung und als Permeations- Sperrschichten zur Erhöhung des Korrosionsschutzes durch Minimierung der Nanoporosität . Alternativ kann es sich bei dem Beschichtungsmaterial auch um metallische oder keramische Partikel handeln. It is also preferably proposed that the particles be admixed as a coating material with the atmospheric plasma jet which causes the hardening of the sol-gel layer. The coating material can in turn be applied with the same plasma generator, with the plasma jet merely being supplied with a suitable precursor for the desired coating. It is preferably a polymerizable precursor. By means of plasma polymerization processes under atmospheric pressure, SiO 2, TiO 2, SnO x , CrO x , diamond-like carbon and polymer layers can be produced in a known manner. The process proceeds from the formation of radicals in the gas phase through collision with surrounding particles and the very intense UV radiation in the plasma, which enables polymerization. The structure of the plasma polymers is close to that of conventional polymers, especially with low energy input per precursor monomer. These precursors (eg HMDSO, TEOS, TiC14, C2H2, etc.) can be added in the highly ionized discharge zone or only in the quasi-neutral plasma zone without interaction of electrons and ions. A special position is the "atmospheric plas a liquid deposition", where droplets are sprayed into the plasma instead of precursor vapor, which prevents damage to fragile organic molecules by ionization. The use of an atmospheric plasma jet according to the invention thus enables curing and surface modification because of the intense (UV) radiation also the production of polymer and oxide ceramic thin layers, whereby the significantly larger working distance gives decisive advantages in the use of 3D objects. The (simultaneous) use of precursors for layer deposition is very advantageous for single-step functionalization during curing, i.e. the use of intermediate layers to increase toughness, hardness or wear resistance and as permeation barrier layers to increase corrosion protection by minimizing the Nanoporosity. Alternatively, the coating material can also be metallic or ceramic particles.
In entsprechender Weise wird eine Beschichtung eines Substrats mit biozider Wirkung vorgeschlagen, die eine ausgehärtete Sol- Gel-Schicht enthaltend Kupfer, Zink, Wolfram und/oder deren Oxide, Metallsalze, oder Titandioxid umfasst, sowie eine Schicht, die aus einem polymerisierten und mittels eines atmosphärischen Plasmastrahles polymerisierbaren Precursor gebildet wird. Bei dem mittels eines atmosphärischen Plasmastrahles polymerisierbaren Precursor handelt es sich vorzugsweise um HMDSO oder TEOS . Das erfindungsgemäße Verfahren lässt sich dabei erweitern, indem mithilfe einer Abfolge von Sol-Gel-Schichtaufträgen und Bestrahlungen mit dem atmosphärischen Plasmastrahl ein Mehrlagenaufbau erfolgt. Durch den Mehrlagenaufbau können hohe Schichtdicken erzielt werden, die die Funktionsfähigkeit der bioziden Beschichtung über lange Zeit aufrechterhalten. Des Weiteren wird eine Beschichtung eines Substrats mit biozider Wirkung vorgeschlagen, die eine ausgehärtete Sol-Gel-Schicht enthaltend Kupfer, Zink, Wolfram und/oder deren Oxide, Metallsalze, oder Titandioxid umfasst, sowie eine Schicht, die aus metallischen oder keramischen Partikeln gebildet wird. Die Erfindung wird in weiterer Folge anhand von Ausführungsbeispielen mithilfe der beiliegenden Figuren näher erläutert. Hierbei zeigen die In a corresponding manner, a coating of a substrate with a biocidal effect is proposed, which comprises a hardened sol-gel layer containing copper, zinc, tungsten and / or their oxides, metal salts, or titanium dioxide, and a layer consisting of a polymerized and by means of a atmospheric plasma jet polymerizable precursor is formed. The precursor polymerizable by means of an atmospheric plasma jet is preferably HMDSO or TEOS. The method according to the invention can be expanded in that a multilayer structure is carried out with the aid of a sequence of sol-gel layer applications and irradiation with the atmospheric plasma jet. Thanks to the multilayer structure, high layer thicknesses can be achieved, which maintain the functionality of the biocidal coating over a long period of time. Furthermore, a coating of a substrate with a biocidal effect is proposed, which comprises a hardened sol-gel layer containing copper, zinc, tungsten and / or their oxides, metal salts, or titanium dioxide, and a layer which is formed from metallic or ceramic particles , The invention is explained in more detail below on the basis of exemplary embodiments with the aid of the attached figures. Here show the
Fig. 1 eine Schnittansicht durch eine mögliche Ausführungsform eines Plasmaerzeugers zur Aushärtung der Sol-Gel-Schicht und zur Zufuhr der bioziden Partikel sowie desFig. 1 is a sectional view through a possible embodiment of a plasma generator for curing the sol-gel layer and for supplying the biocidal particles and the
Beschichtungsmaterials , Coating material,
Fig. 2a eine schematische Darstellung einer möglichenFig. 2a is a schematic representation of a possible
Ausführung des erfindungsgemäßen Verfahrens, Execution of the method according to the invention,
Fig. 2b eine schematische Darstellung einer weiteren möglichen Ausführung des erfindungsgemäßen Verfahrens, 2b is a schematic representation of a further possible embodiment of the method according to the invention,
Fig. 3a eine schematische Darstellung einer durch das erfindungsgemäße Verfahren hergestellten Beschichtung, und die 3a shows a schematic representation of a coating produced by the method according to the invention, and the
Fig. 3b eine schematische Darstellung eines durch das erfindungsgemäße Verfahren hergestellten Mehrlagenaufbaus . 3b shows a schematic representation of a multilayer structure produced by the method according to the invention.
Zunächst wird anhand der Fig. 1 eine mögliche Ausführungsform eines Plasmaerzeugers 1 zur Aushärtung einer Sol-Gel-Schicht S und zur Zufuhr von Partikel P als Ein- oder Anlagerungen der Sol-Gel-Schicht S beschrieben. Die Vorrichtung umfasst einen Plasmaerzeuger 1, der eine Kathode 2 und eine Anode 5 aufweist. Die Kathode 2 ist zylindrisch ausgeführt und weist an ihrem freien Ende einen konischen Endbereich 3 auf, der im gezeigten Ausführungsbeispiel in einen Austrittskanal 4 für den Plasmastrahl AP ragt. Die Anode 5 ist koaxial zur Kathode 2 angeordnet, wobei die Kathode 2 und die Anode 5 mit einer steuerbaren Spannungsquelle 6 verbunden sind. Zwischen der Kathode 2 und der Anode 5 wird eine Gleichspannung im Bereich von 10-30 V bei einem Strom von 60-500 A angelegt. Die elektrische Leistung des Plasmaerzeugers bewegt sich dabei im Bereich von 600-10000 W. Die Kathode 2 kann wahlweise in ihrem Inneren mit einer Kathodenkühlung (in der Fig. 1 nicht dargestellt) versehen sein. Des Weiteren sind im Mantelkörper des Plasmaerzeugers 1 Kühlmittelkanäle 10 vorgesehen, die mit einer Kühlmittelquelle 11 verbunden sind und den Plasmaerzeuger 1 kühlen. 1, a possible embodiment of a plasma generator 1 for curing a sol-gel layer S and for supplying particles P as deposits or deposits of the sol-gel layer S is described. The device comprises a plasma generator 1, which has a cathode 2 and an anode 5. The cathode 2 is cylindrical and has at its free end a conical end region 3 which, in the exemplary embodiment shown, projects into an outlet channel 4 for the plasma jet AP. The anode 5 is arranged coaxially with the cathode 2, the cathode 2 and the anode 5 being connected to a controllable voltage source 6. A direct voltage in the range of 10-30 V at a current of 60-500 A is applied between the cathode 2 and the anode 5. The electrical power of the plasma generator moves in the Range of 600-10000 W. The inside of the cathode 2 can optionally be provided with cathode cooling (not shown in FIG. 1). Furthermore, coolant channels 10 are provided in the jacket body of the plasma generator 1, which are connected to a coolant source 11 and cool the plasma generator 1.
Die Kathode 2 und die Anode 5 begrenzen einen Arbeitsgaskanal 7, der mit einer steuerbaren Arbeitsgasquelle 8 verbunden ist. Als Arbeitsgas können beispielsweise Argon, Helium, Stickstoff oder vorrangig inerte Mischgase wie etwa Argon-Wasserstoff- Mischgase oder auch Luft verwendet werden. Der Arbeitsgaskanal 7 mündet in den Austrittskanal 4, der sich über eine Ausströmöffnung 9 in die umgebende Atmosphäre öffnet. Im Betrieb wird an die Kathode 2 und die Anode 5 eine Spannung angelegt, die ausreichend hoch gewählt ist um zwischen dem spitz zulaufenden Endbereich der Kathode 2 und der die Kathode 2 umgebenden Anode 5 einen Lichtbogen zu zünden. Diese elektrische Entladung ionisiert das den Arbeitskanal 7 durchströmende Arbeitsgas, das in weiterer Folge als Plasma den Austrittskanal 4 durchströmt und als Plasmastrahl AP über die Ausströmöffnung 9 in die umgebende Atmosphäre austritt . Der an die Ausströmöffnung 9 angrenzende Atmosphärenbereich wird dabei in weiterer Folge als Ausströmbereich 14 bezeichnet und wird in der Fig. 1 mit punktierten Linien angedeutet. Die Ausströmweite des Plasmastrahls AP in der umgebenden Atmosphäre hängt insbesondere vom Betriebsdruck der Arbeitsgasquelle 8 und des angelegten Stromes an Kathode 2 und Anode 5 ab. The cathode 2 and the anode 5 delimit a working gas channel 7, which is connected to a controllable working gas source 8. For example, argon, helium, nitrogen or primarily inert mixed gases such as argon-hydrogen mixed gases or also air can be used as the working gas. The working gas channel 7 opens into the outlet channel 4, which opens into the surrounding atmosphere via an outflow opening 9. In operation, a voltage is applied to the cathode 2 and the anode 5 which is selected to be sufficiently high to ignite an arc between the tapering end region of the cathode 2 and the anode 5 surrounding the cathode 2. This electrical discharge ionizes the working gas flowing through the working channel 7, which subsequently flows through the outlet channel 4 as a plasma and exits as a plasma jet AP through the outflow opening 9 into the surrounding atmosphere. The atmospheric area adjoining the outflow opening 9 is subsequently referred to as the outflow area 14 and is indicated in FIG. 1 with dotted lines. The outflow of the plasma jet AP in the surrounding atmosphere depends in particular on the operating pressure of the working gas source 8 and the current applied to the cathode 2 and anode 5.
Am Plasmaerzeuger 1 ist an seinem ausströmseitigen Ende ferner eine Halterung 12 angeordnet, über die eine Zufuhreinrichtung eines entsprechenden Precursormaterials PP für einen ersten Typ einzubringender Partikel P sowie den Precursor PB für einen als Beschichtungsmaterial B dienenden, zweiten Typ einzubringender Partikel P befestigt ist . DieA holder 12 is also arranged on the plasma generator 1 at its outflow end, via which a feed device of a corresponding precursor material PP for a first type of particles P to be introduced and the precursor PB for a second type serving as coating material B. particle P to be introduced is attached. The
Zufuhreinrichtung umfasst im gezeigten Ausführungsbeispiel zwei Zufuhrrohre 13, die einlassseitig jeweils mit einem Verdampfer 15 für das Precursormaterial PP für einen ersten Typ einzubringender Partikel P sowie für den Precursor PB für einen als Beschichtungsmaterial B dienenden, zweiten Typ einzubringender Partikel P verbunden sind und auslassseitig jeweils eine Austrittsöffnung 16 aufweisen, die in den Ausströmbereich 14 gerichtet sind. Der Verdampfer 15 ist mit zumindest einem Vorratsbehälter 17 für den Precursor PB oder für das Precursormaterial PP verbunden. In the exemplary embodiment shown, the feed device comprises two feed tubes 13, each of which is connected on the inlet side to an evaporator 15 for the precursor material PP for a first type of particle P to be introduced and for the precursor PB for a second type of particle P to be used as coating material B, and one on the outlet side Have outlet opening 16 which are directed into the outflow region 14. The evaporator 15 is connected to at least one storage container 17 for the precursor PB or for the precursor material PP.
Die Fig. 2a zeigt eine schematische Darstellung einer möglichen Ausführung des erfindungsgemäßen Verfahrens als kontinuierliches Verfahren, bei dem das Substrat 18 von einem Ort des Auftrages einer Sol-Gel-Schichtmatrix SM zum Plasmaerzeuger 1 bewegt wird. Bei gewünschter Herstellung eines Multilagenaufbaus kann auch eine abwechselnde Positionierung zwischen dem Ort des Auftrages der Sol-Gel- Schichtmatrix SM und dem Plasmaerzeuger 1 eingenommen werden ( strichlierter Pfeil in der Fig. 2a) . Die Fig. 2b zeigt eine schematische Darstellung einer weiteren möglichen Ausführung des erfindungsgemäßen Verfahrens, bei dem eine gleichzeitige Oberflächenbehandlung des Substrats 18 durch den Auftrag einer Sol-Gel-Schichtmatrix SM und Plasmabehandlung erfolgt. FIG. 2a shows a schematic representation of a possible embodiment of the method according to the invention as a continuous method, in which the substrate 18 is moved from a place where a sol-gel layer matrix SM is applied to the plasma generator 1. If a multilayer structure is desired, alternating positioning between the location of the application of the sol-gel layer matrix SM and the plasma generator 1 can also be assumed (dashed arrow in FIG. 2a). 2b shows a schematic representation of a further possible embodiment of the method according to the invention, in which a simultaneous surface treatment of the substrate 18 is carried out by applying a sol-gel layer matrix SM and plasma treatment.
Zunächst erfolgt das Aufträgen einer Sol-Gel-Schichtmatrix SM auf das Substrat 18, im gezeigten Ausführungsbeispiel der Fig. 2 etwa mithilfe eines Sprühverfahrens. Verfahren zum Aufträgen einer Sol-Gel-Schichtmatrix SM auf einem Substrat 18 sind hinlänglich bekannt. Dabei können mittels der Sol-Gel-Synthese aus kolloidalen Dispersionen anorganische oder organisch anorganische (hybrid-polymere) Beschichtungen hergestellt werden, wobei die chemische Verfahrenstechnik zunächst eine Hydrolyse-Reaktion des Alkoholate-Vorläuffers erfordert (Bildung von „Sol-Teilchen"). Diese werden durch Säure- oder Basenzugabe katalytisch zu Ketten kondensiert. Vorläufermoleküle basieren oftmals auf Silizium- (TEOS, TMOS) , Titan- oder Zirkon-Verbindungen, wobei durch Einbindung entsprechender organo-funktioneller Siliziumverbindungen in das anorganische Netzwerk bei der Kondensation die Eigenschaften der resultierenden Sol-Gel-Schichten S gezielt eingestellt werden. Möglichkeiten umfassen die Flexibilisierung des Netzwerks, Einstellung der Aushärtebedingungen, Ausbildung eines zusätzlichen organischen Netzwerks (neben dem anorganischen) , Variation der Oberflächenenergie, oder die Erhöhung der Kratzbeständigkeit durch Co-Kondensation mit Metall-Alkoxiden wie z. B. Aluminium-Alkoxid. Alle wesentlichen Grundreaktionen, d.h. Hydrolyse und die anschließenden Kondensationsreaktion zwischen den entstehenden reaktiven Spezies zur Bildung des 3D-Netzwerks , sind dynamische Prozesse vieler ineinandergreifender Gleichgewichtsreaktionen und können über den pH-Wert, Temperatur oder Vorläufermolekül-Konzentrationen gesteuert werden. Alternativ zu Sprühverfahren können Sol-Gel- Schichten S auch durch Tauchverfahren oder Rotationsbeschichtung (Spincoating) auf 3D-Oberflächen aufgebracht werden. First, a sol-gel layer matrix SM is applied to the substrate 18, in the exemplary embodiment shown in FIG. 2, for example using a spraying method. Methods for applying a sol-gel layer matrix SM to a substrate 18 are well known. In this case, sol or gel synthesis can be used to produce inorganic or organically inorganic (hybrid polymer) coatings from colloidal dispersions, chemical process engineering first requiring a hydrolysis reaction of the alcoholate precursor (Formation of “sol particles”). These are condensed catalytically into chains by adding acid or base. Precursor molecules are often based on silicon (TEOS, TMOS), titanium or zirconium compounds, with the incorporation of appropriate organo-functional silicon compounds in the inorganic network in the condensation, the properties of the resulting sol-gel layers S can be set in a targeted manner.Possibilities include making the network more flexible, setting the curing conditions, forming an additional organic network (in addition to the inorganic), varying the surface energy, or increasing the Scratch resistance through co-condensation with metal alkoxides such as aluminum alkoxide All essential basic reactions, ie hydrolysis and the subsequent condensation reaction between the resulting reactive species to form the 3D network, are dynamic processes of many interlocking equilibrium reactions and can be controlled via pH, temperature or precursor molecule concentrations. As an alternative to the spraying process, sol-gel layers S can also be applied to 3D surfaces by immersion processes or spin coating.
Der Sol-Gel-Schichtauftrag kann mittels einer Sol-Gel- Schichtmatrix SM erfolgen, die bereits biozide Substanzen enthält, etwa biozid wirkende quaternäre Ammoniumsalze, insbesondere Q-POSS. Zudem kann vorgesehen sein, dass der Sol- Gel-Schichtauftrag mittels einer Sol-Gel-Schichtmatrix SM erfolgt, die Cer enthält, um die Korrosionsbeständigkeit der ausgehärteten Sol-Gel-Schicht S zu erhöhen. The sol-gel layer application can be carried out by means of a sol-gel layer matrix SM which already contains biocidal substances, for example quaternary ammonium salts with a biocidal effect, in particular Q-POSS. Provision can also be made for the sol-gel layer to be applied by means of a sol-gel layer matrix SM which contains cerium in order to increase the corrosion resistance of the hardened sol-gel layer S.
Als Substrat 18 können metallische Werkstoffe, aber auch Kunststoffe, insbesondere Thermoplasten, verwendet werden, da aufgrund des indirekt übertragenen Lichtbogens bei der anschließenden Plasmabehandlung sowohl elektrisch leitfähige als auch nicht-leitfähige Substrate wie glasartige Werkstoffe, Verbundwerkstoffe (CFK/GFK) oder Kunststoffe beschichtet werden können. Metallic materials, but also plastics, in particular thermoplastics, can be used as substrate 18, since due to the indirectly transmitted arc in the subsequent plasma treatment, both electrically conductive and non-conductive substrates such as glass-like materials, composite materials (CFRP / GFRP) or plastics can be coated.
Im gezeigten Ausführungsbeispiel der Fig. 2a wird das Substrat 18 nach dem Aufträgen der Sol-Gel-Schicht S dem Plasmastrahl AP eines Plasmaerzeugers 1 ausgesetzt, um Partikel P eines ersten Typs, etwa biozide Partikel, in die Sol-Gel-Schicht S einzubringen. Falls die Sol-Gel-Schicht S bereits biozide Substanzen enthält, kann dieser Schritt auch entfallen. Die Partikel P werden dabei in Form eines entsprechenden Precursormaterials PP dem Verdampfer 15 und in weiterer Folge mittels eines Trägergases dem Plasmastrahl AP beigefügt und in Form der Partikel P auf das Substrat 18 aufgetragen, wo sie in die Sol-Gel-Schicht S eingelagert werden. Im Rahmen der vorliegenden Erfindung werden vorzugsweise biozide Partikel P, die Kupfer, Zink oder Wolfram und/oder deren Oxide, oder Titandioxid enthalten, vorgeschlagen. Die Fig. 2b zeigt eine schematische Darstellung einer weiteren möglichen Ausführung des erfindungsgemäßen Verfahrens, bei dem eine gleichzeitige Oberflächenbehandlung des Substrats 18 durch den Auftrag einer Sol-Gel-Schicht S und Einbringen der Partikel P durch das atmosphärische Plasma AP erfolgt. In the exemplary embodiment shown in FIG. 2a, the substrate 18 is exposed to the plasma jet AP of a plasma generator 1 after the sol-gel layer S has been applied, in order to introduce particles P of a first type, for example biocidal particles, into the sol-gel layer S. If the sol-gel layer S already contains biocidal substances, this step can also be omitted. The particles P are added in the form of a corresponding precursor material PP to the evaporator 15 and subsequently to the plasma jet AP by means of a carrier gas and applied in the form of the particles P to the substrate 18, where they are embedded in the sol-gel layer S. In the context of the present invention, biocidal particles P which contain copper, zinc or tungsten and / or their oxides or titanium dioxide are preferably proposed. 2b shows a schematic representation of a further possible embodiment of the method according to the invention, in which a simultaneous surface treatment of the substrate 18 is carried out by applying a sol-gel layer S and introducing the particles P through the atmospheric plasma AP.
Nach dem Aufträgen der Sol-Gel-Schicht S erfolgt erfindungsgemäß die Aushärtung der Sol-Gel-Schicht S durch Bestrahlung mit einem auf die Sol-Gel-Schicht S gerichteten, atmosphärischen Plasmastrahl AP. Hierbei können dem die Aushärtung der Sol-Gel-Schicht S bewirkenden, atmosphärischen Plasmastrahl AP als Beschichtungsmaterial B dienende Partikel P eines zweiten Typs beigemengt werden. Der Auftrag dieses Beschichtungsmaterials B kann wiederum mit demselben Plasmaerzeuger 1 erfolgen, wobei dem Plasmastrahl AP lediglich ein geeigneter Precursor PB für die gewünschte Beschichtung zugeführt wird. Vorzugsweise handelt es dabei um einen polymerisierbaren Precursor PB. Die Zugabe dieser Precursoren PB, vorzugsweise HMDSO oder TEOS, zum Plasmastrahl AP kann in der hochionisierten Entladungszone oder erst in der Zone von quasineutralem Plasma ohne Wechselwirkung von Elektronen und Ionen erfolgen. Die erfindungsgemäße Verwendung eines atmosphärischen Plasmastrahls AP ermöglicht somit neben der Aushärtung und Oberflächenmodifikation aufgrund der intensiven (UV- ) Strahlung auch die Herstellung von Polymer- und oxidkeramischen Dünnschichten, wobei durch den deutlich größeren Arbeitsabstand entscheidende Vorteile in der Anwendung an 3D-Objekten erzielt werden. After the application of the sol-gel layer S, the sol-gel layer S is cured according to the invention by irradiation with an atmospheric plasma jet AP directed onto the sol-gel layer S. Particles P of a second type serving as coating material B can be admixed with the atmospheric plasma jet AP causing the hardening of the sol-gel layer S. This coating material B can in turn be applied with the same plasma generator 1, the plasma jet AP merely having a suitable precursor PB for the desired coating is fed. It is preferably a polymerizable precursor PB. These precursors PB, preferably HMDSO or TEOS, can be added to the plasma jet AP in the highly ionized discharge zone or only in the zone of quasi-neutral plasma without interaction of electrons and ions. The use of an atmospheric plasma jet AP according to the invention thus enables not only curing and surface modification due to the intense (UV) radiation, but also the production of polymer and oxide-ceramic thin layers, the decisive advantage being achieved in the use of 3D objects due to the significantly larger working distance.
Die Aushärtung der Sol-Gel-Schicht mittels atmosphärischem Plasmastrahl AP kann rascher erfolgen als mit herkömmlicher thermischer Behandlung, sodass höhere Schichtdicken verwirklicht werden können, und insbesondere auch ein Mehrlagenaufbau der aufgebrachten Schicht wirtschaftlich möglich ist, indem mehrere Sol-Gel-Schichten S jeweils nach Aushärtung durch das atmosphärische Plasma AP nacheinander auf das Substrat 18 aufgebracht werden, wie anhand der Fig. 3 erläutert wird. The hardening of the sol-gel layer by means of atmospheric plasma jet AP can be carried out more quickly than with conventional thermal treatment, so that higher layer thicknesses can be achieved, and in particular a multilayer structure of the applied layer is economically possible by using several sol-gel layers S each Curing by the atmospheric plasma AP can be applied successively to the substrate 18, as will be explained with reference to FIG. 3.
Hierbei zeigt die Fig. 3a eine schematische Darstellung einer durch das erfindungsgemäße Verfahren hergestellten Beschichtung umfassend eine Sol-Gel-Schicht S und eine Schicht eines Beschichtungsmaterials B, und die Fig. 3b eine schematische Darstellung eines durch das erfindungsgemäße Verfahren hergestellten Mehrlagenaufbaus umfassend zwei Sol-Gel-Schichten S und zwei Schichten eines Beschichtungsmaterials B. In die Sol-Gel-Schicht S sind dabei biozide Partikel P etwa in Form biozider Metall (oxid) partikel eingebettet. Zudem kann die Sol- Gel-Schicht S biozid wirkende quaternäre Ammoniumsalze enthalten, um die biozide Wirksamkeit der Beschichtung noch zu erhöhen. Zudem kann vorgesehen sein, dass die Sol-Gel-Schicht S Cer-basierte Korrosionsinhibitoren enthält, um die Korrosionsbeständigkeit der ausgehärteten Sol-Gel-Schicht S zu erhöhen. Des Weiteren umfasst die Beschichtung gemäß der Fig. 3a und 3b eine Schicht eines Beschichtungsmaterials B, die im gezeigten Ausführungsbeispiel aus einem polymerisierten und mittels eines atmosphärischen Plasmastrahles AP polymerisierbaren Precursor PB gebildet wird. Bei dem mittels eines atmosphärischen Plasmastrahles AP polymerisierbaren Precursor PB handelt es sich etwa um HMDSO oder TEOS . Diese Schicht kann als Permeations-Sperrschicht bezeichnet werden, da sie eine räumliche Abgrenzung des durch die Partikel P der Sol- Gel-Schicht S gegebenen bioziden Reservoirs darstellt. 3a shows a schematic illustration of a coating produced by the method according to the invention, comprising a sol-gel layer S and a layer of a coating material B, and FIG. 3b shows a schematic illustration of a multilayer structure comprising two sol- Gel layers S and two layers of a coating material B. Biocidal particles P are embedded in the sol-gel layer S, for example in the form of biocidal metal (oxide) particles. In addition, the sol-gel layer S can contain biocidal quaternary ammonium salts in order to further increase the biocidal effectiveness of the coating. It can also be provided that the sol-gel layer S contains cerium-based corrosion inhibitors to increase the corrosion resistance of the hardened sol-gel layer S. Furthermore, the coating according to FIGS. 3a and 3b comprises a layer of a coating material B which, in the exemplary embodiment shown, is formed from a polymerized precursor PB which can be polymerized by means of an atmospheric plasma jet AP. The precursor PB polymerizable by means of an atmospheric plasma jet AP is, for example, HMDSO or TEOS. This layer can be referred to as a permeation barrier layer since it represents a spatial delimitation of the biocidal reservoir given by the particles P of the sol-gel layer S.
Durch den in der Fig. 3 gezeigten Mehrlagenaufbau können hohe Schichtdicken erzielt werden, die die Funktionsfähigkeit der bioziden Beschichtung über lange Zeit aufrechterhalten. Die gegenständliche Erfindung ermöglicht somit ein Verfahren zur Herstellung dauerhafter, harter, Korrosions-, Abrieb- und Verschleißbeständigen Beschichtungen mit biozider Wirkung, das zudem auch wirtschaftlich einsetzbar ist. The multilayer structure shown in FIG. 3 enables high layer thicknesses to be achieved which maintain the functionality of the biocidal coating over a long period of time. The subject invention thus enables a process for producing durable, hard, corrosion, abrasion and wear resistant coatings with a biocidal effect, which is also economically applicable.
Claims
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP19724810.7A EP3807449A1 (en) | 2018-06-14 | 2019-05-15 | Method for coating a substrate |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| ATA50481/2018A AT521294B1 (en) | 2018-06-14 | 2018-06-14 | Process for coating a substrate |
| ATA50481/2018 | 2018-06-14 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO2019238347A1 true WO2019238347A1 (en) | 2019-12-19 |
Family
ID=66589556
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/EP2019/062466 Ceased WO2019238347A1 (en) | 2018-06-14 | 2019-05-15 | Method for coating a substrate |
Country Status (3)
| Country | Link |
|---|---|
| EP (1) | EP3807449A1 (en) |
| AT (1) | AT521294B1 (en) |
| WO (1) | WO2019238347A1 (en) |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20080193674A1 (en) * | 2004-09-30 | 2008-08-14 | Roberto Siegert | Production of a Gas-Tight, Crystalline Mullite Layer by Using a Thermal Spraying Method |
| DE102008029681A1 (en) * | 2008-06-23 | 2009-12-24 | Plasma Treat Gmbh | Method and device for applying a layer, in particular a self-cleaning and / or antimicrobial photocatalytic layer, to a surface |
| WO2011022011A1 (en) * | 2009-08-20 | 2011-02-24 | Certainteed Corporation | Roofing granules, roofing products including such granules, and process for preparing same |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE10353756A1 (en) * | 2003-11-17 | 2005-06-30 | Bio-Gate Bioinnovative Materials Gmbh | layer material |
| DE102007041544A1 (en) * | 2007-08-31 | 2009-03-05 | Universität Augsburg | Method of making DLC layers and doped polymers or diamond-like carbon layers |
| DE102008001014A1 (en) * | 2008-04-04 | 2009-10-08 | Bio-Gate Ag | layer material |
| DE102009030876B4 (en) * | 2009-06-29 | 2011-07-14 | Innovent e.V., 07745 | Method for coating a substrate |
-
2018
- 2018-06-14 AT ATA50481/2018A patent/AT521294B1/en active
-
2019
- 2019-05-15 EP EP19724810.7A patent/EP3807449A1/en not_active Withdrawn
- 2019-05-15 WO PCT/EP2019/062466 patent/WO2019238347A1/en not_active Ceased
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20080193674A1 (en) * | 2004-09-30 | 2008-08-14 | Roberto Siegert | Production of a Gas-Tight, Crystalline Mullite Layer by Using a Thermal Spraying Method |
| DE102008029681A1 (en) * | 2008-06-23 | 2009-12-24 | Plasma Treat Gmbh | Method and device for applying a layer, in particular a self-cleaning and / or antimicrobial photocatalytic layer, to a surface |
| WO2011022011A1 (en) * | 2009-08-20 | 2011-02-24 | Certainteed Corporation | Roofing granules, roofing products including such granules, and process for preparing same |
Also Published As
| Publication number | Publication date |
|---|---|
| AT521294A1 (en) | 2019-12-15 |
| AT521294B1 (en) | 2020-02-15 |
| EP3807449A1 (en) | 2021-04-21 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP2486163B1 (en) | Atmospheric pressure plasma method for producing surface-modified particles and coatings | |
| DE60015725T2 (en) | Production of materials | |
| EP2054166B1 (en) | Method and device for producing a coating | |
| EP3094761B1 (en) | Plasma coating method for depositing a functional layer, and depositing device | |
| DE102008037159A1 (en) | Apparatus and method for the plasma treatment of hollow bodies | |
| DE102008029681A1 (en) | Method and device for applying a layer, in particular a self-cleaning and / or antimicrobial photocatalytic layer, to a surface | |
| DE102011076806A1 (en) | Apparatus and method for producing a cold, homogeneous plasma under atmospheric pressure conditions | |
| EP3943277B1 (en) | Device and method for the additive manufacturing of components | |
| DE112017001370T5 (en) | Plasma generating device | |
| EP2257656B1 (en) | Method for producing a coating through cold gas spraying | |
| DE102008064134B4 (en) | Process for coating objects by means of a low-pressure plasma | |
| AT521294B1 (en) | Process for coating a substrate | |
| DE10223865B4 (en) | Process for the plasma coating of workpieces | |
| DE102010005762A1 (en) | Cleaning process for coating systems | |
| DE102014103025A1 (en) | Method for coating a substrate, use of the substrate and device for coating | |
| DE102006015591B3 (en) | Organic material with a catalytically coated surface and process for its production | |
| DE102008056968B4 (en) | A method of depositing a nanocomposite layer on a substrate by chemical vapor deposition | |
| DE102016104128A1 (en) | Method for coating a component surface, coated component and use of a precursor material | |
| EP0815283A1 (en) | Plasma chamber | |
| EP1872637B1 (en) | Plasma coating device and method | |
| EP2746424B1 (en) | Evaporation source | |
| WO2022027077A1 (en) | Method for producing an antimicrobial coating | |
| DE102013220841A1 (en) | Method for pretreatment of a substrate surface and method for coating the substrate surface | |
| DE3211282A1 (en) | Process for coating glass articles | |
| DE102010014552A1 (en) | Coating a substrate surface using a plasma beam or plasma beams, comprises directing a beam of an atmospheric low-temperature plasma to the substrate surface according to respective plasma coating nozzle in opposition to thermal injection |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 19724810 Country of ref document: EP Kind code of ref document: A1 |
|
| NENP | Non-entry into the national phase |
Ref country code: DE |
|
| WWE | Wipo information: entry into national phase |
Ref document number: 2019724810 Country of ref document: EP |
|
| ENP | Entry into the national phase |
Ref document number: 2019724810 Country of ref document: EP Effective date: 20210114 |
|
| WWW | Wipo information: withdrawn in national office |
Ref document number: 2019724810 Country of ref document: EP |