EP3008139A1 - Beschichtungsmassen, enthaltend leitfähige füllstoffe - Google Patents

Beschichtungsmassen, enthaltend leitfähige füllstoffe

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Publication number
EP3008139A1
EP3008139A1 EP14726627.4A EP14726627A EP3008139A1 EP 3008139 A1 EP3008139 A1 EP 3008139A1 EP 14726627 A EP14726627 A EP 14726627A EP 3008139 A1 EP3008139 A1 EP 3008139A1
Authority
EP
European Patent Office
Prior art keywords
organic
weight
fillers
coating
ionic liquid
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.)
Withdrawn
Application number
EP14726627.4A
Other languages
German (de)
English (en)
French (fr)
Inventor
Andreas Eichfelder
Fabien Jean Brand
Christian Krausche
Laszlo Szarvas
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
BASF SE
Original Assignee
BASF SE
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by BASF SE filed Critical BASF SE
Priority to EP14726627.4A priority Critical patent/EP3008139A1/de
Publication of EP3008139A1 publication Critical patent/EP3008139A1/de
Withdrawn legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
    • C09D5/24—Electrically-conducting paints
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
    • C09D5/34—Filling pastes
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
    • C09D7/40—Additives
    • C09D7/60—Additives non-macromolecular
    • C09D7/63—Additives non-macromolecular organic
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J9/00—Adhesives characterised by their physical nature or the effects produced, e.g. glue sticks
    • C09J9/02—Electrically-conducting adhesives
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K3/00—Materials not provided for elsewhere
    • C09K3/10—Materials in mouldable or extrudable form for sealing or packing joints or covers
    • C09K3/1006—Materials in mouldable or extrudable form for sealing or packing joints or covers characterised by the chemical nature of one of its constituents
    • D—TEXTILES; PAPER
    • D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H21/00—Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties
    • D21H21/14—Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties characterised by function or properties in or on the paper

Definitions

  • the present invention relates to a use of organic fillers as additives for coating compositions or sealants, which are characterized in that the organic fillers consist of at least 20 wt .-% of an organic polymer and an ionic liquid.
  • organic fillers consist of at least 20 wt .-% of an organic polymer and an ionic liquid.
  • various additives in liquid and solid form are known. Liquid additives can dissolve in the masses and form conductive structures, e.g. thin aqueous layers at the interface with the ambient air that allow charge transport. Insoluble constituents can form a percolation path by mutual contact, through which electrical charges can be transported.
  • Ionic liquids are salts with a maximum melting point of 150 ° C.
  • WO 2007/1 15750 describes coating compositions which contain ionic liquids and thus have antistatic properties. These are floor coatings with layer thicknesses from 2 mm to 20 mm. With such thick coatings, conductive fillers such as graphite, carbon black, metal oxides or fibers such as carbon fibers are generally required in addition, which build up a conductive structure in the coating to dissipate charges into the floor.
  • Liquid additives can easily exude from the coating or molding compounds, thereby degrading the antistatic properties of the compositions over time. Also, liquid additives can simultaneously act as a plasticizer; a softening effect is often undesirable.
  • solid additives usually reduces the mechanical strengths when percolation has been achieved.
  • most conductive fillers are colored or even black; common conductive solids are e.g. Carbon and metals or metal oxides in various modifications. This has an influence on the viable color variety in the final product, transparent coating compositions are generally not possible when using such solid additives.
  • WO 201 1/069960 discloses the use of polar, thermoplastic polymers which contain ionic liquids as antistatic additives for non-polar polymers, such as polyolefins or polystyrene.
  • polar, thermoplastic polymers polyurethanes and polyamides are mentioned among others.
  • Ionic liquids are mixed by suitable methods with the polar polymer. From the preserved, antistatic equipped Polymers and the non-polar polymers can now be prepared by thermoplastic processing antistatic polymer blends.
  • Object of the present invention were antistatic coating compositions and antistatic coatings obtained therefrom, which are easy to prepare and have good antistatic properties.
  • the antistatic properties should be retained over as long a period as possible to the highest possible extent.
  • the performance properties of the coating compositions should as far as possible not be impaired.
  • antistatic, transparent coatings should be possible.
  • the object of the invention was, in particular, also coating compositions for floors which have the above properties and which do not require any additional conductive fillers.
  • Coating compositions containing the organic fillers and coatings made therefrom have also been found.
  • floor coating compositions and floor coatings produced therefrom have also been found.
  • the organic fillers are preferably fillers which are present as solids under standard conditions (20 ° C., 1 bar).
  • the organic fillers consist of at least 20% by weight, in particular at least 50% by weight and in a particular embodiment at least 70% by weight of an organic polymer.
  • Suitable organic polymers are any polymers.
  • they are thermoplastically processable polymers, in particular they are thermoplastically processable polymers which have sufficient hardness and can therefore be ground well into powders.
  • the Shore D value is a measure of the hardness of polymers.
  • the Shore D value corresponds to the penetration depth of a truncated cone with a spherical tip with a radius of 0.1 mm and an opening angle of 30 ° with a contact force of the frustum of 50 Newton on the surface of the polymer.
  • polar polymers in particular polyamides, polyurethanes, polyureas or polyesters.
  • the organic polymer is polyamide or polyurethane, in particular thermoplastic polyamide or thermoplastic polyurethane.
  • Preferred polyurethanes are those which are composed of more than 60% by weight, particularly preferably more than 80% by weight, of diisocyanates and diols.
  • Suitable diisocyanates are aliphatic or aromatic diisocyanates.
  • Particularly suitable aliphatic diisocyanates are C 4 -C 10 -alkylene diisocyanates, in particular hexamethylene diisocyanate, and cycloaliphatic diisocyanates, in particular isophorone diisocyanate.
  • Aromatic diisocyanates are understood here to mean those having at least one aromatic group which may be substituted by alkyl or alkylene groups.
  • aromatic diisocyanates in particular diphenylmethane diisocyanate and toluene diisocyanate may be mentioned. Frequently, mixtures of different diisocyanates are used for the production of polyurethanes.
  • Suitable diols are short chain diols, e.g. C2 to C10 alkylene diols or long chain
  • Diols such as polyether or polyester diols are frequently used. Mixtures of different diols, in particular combinations of short-chain and long-chain diols, are used for the preparation of polyurethanes.
  • the polyurethanes may be e.g. additionally also from compounds with more than two isocyanate groups, e.g. Isocyanurates, or more than two hydroxyl groups to be set up when a desired degree of branching is to be adjusted. Compounds with only one isocyanate group or only one hydroxyl group are used to adjust the chain length and thus the molecular weight.
  • Preferred polyamides are those which are composed of more than 60% by weight, in particular more than 80% by weight, of diamines, dicarboxylic acids, aminocarboxylic acids and lactams.
  • Polyamides are polycondensates of diamines, e.g. aliphatic diamines, such as C 2 to C 12 alkylenediamines, especially hexamethylenediamine, and dicarboxylic acids, e.g. aliphatic or aromatic dicarboxylic acids, such as C2- to C16-alkylenedicarboxylic acids such as adipic acid, sebacic acid, azelaic acid or dodecanedioic acid.
  • polystyrene resin e.g., polystyrene resin
  • lactams e.g. Caprolactam or laurolactam
  • the polyamides may also contain further structural components, e.g. consist of adjusting a degree of branching or the molecular weight.
  • a particularly preferred polymer is polyamide 6 (polycondensation product of caprolactam) which is e.g. available as Ultramid B from BASF.
  • the organic fillers contain an ionic liquid.
  • ionic liquid is understood as meaning salts (compounds of cations and anions) which at normal pressure (1 bar) have a melting point of less than 150 ° C., preferably less than 150 ° C. ner 100 ° C, more preferably less than 50 ° C have. In a particular embodiment, it is salt, which are liquid at 20 ° C.
  • ionic liquid will be understood below to mean both individual and mixtures of different ionic liquids.
  • Preferred ionic liquids contain an organic compound as a cation (organic cation). Depending on the valence of the anion, the ionic liquid may contain other cations, including metal cations, in addition to the organic cation.
  • the cations of preferred ionic liquids are exclusively organic cations.
  • Suitable organic cations are in particular organic compounds with heteroatoms, such as nitrogen, sulfur, oxygen or phosphorus; in particular, the organic cations are compounds with an ammonium group (ammonium cations), an oxonium group (oxonium cations), a sulfonium group (sulfonium cations) or a phosphonium group (phosphonium cations) ,
  • the organic cations of the ionic liquids are ammonium cations, hereunder non-aromatic compounds with located positive charge on a nitrogen atom with four substituents (quaternary ammonium compounds) or
  • Preferred is a quaternary ammonium cation or a cation having a delocalized positive charge heterocyclic ring system or a localized positive charge on one of the ring atoms.
  • Suitable quaternary ammonium cations are, for example, those having three or four aliphatic substituents, for example C 1 - to C 12 -alkyl groups or C 1 - to C 12 -alkyl groups substituted by one or two hydroxyl groups; wherein in the case of three aliphatic substituents, the fourth substituent is preferably a hydroxyl group.
  • Suitable cation with a heterocyclic ring system are monocyclic, bicyclic, aromatic or non-aromatic ring systems. Examples include bicyclic systems, as described in WO 2008/043837. In the bicyclic systems of
  • WO 2008/043837 are diazabicyclo derivatives, preferably from a 7- and a 6-ring, which contain an amidinium group; in particular the 1,8-diazabicyclo (5.4.0) undec-7-enium cation may be mentioned.
  • ionic liquids with cations which contain a heterocyclic ring system having one or two nitrogen atoms as part of the ring system.
  • organic cations come into consideration, e.g. Pyridinium cations, pyridazinium cations, pyrimidinium cations, pyrazinium cations, imidazolium cations, pyrazolium cations, pyrazolinium cations, imidazolinium cations, thiazolium cations, triazolium cations, pyrrolidinium cations and imidazolidinium cations. These cations are e.g. in WO 2005/1 13702.
  • the nitrogen atoms are in each case by a hydrogen atom or an organic group having generally not more than 20 C atoms, preferably a hydrocarbon group, in particular a C1 to C16 alkyl group, in particular one C1 to C10, more preferably substituted a C1 to C4 alkyl groups.
  • the carbon atoms of the ring system can also be substituted by organic groups having generally not more than 20 C atoms, preferably a hydrocarbon group, in particular a C1 to C16 alkyl group, in particular a C1 to C10, particularly preferably a C1 to C4 alkyl groups.
  • ammonium cations are quaternary ammonium cations, imidazolium cations, pyrimidinium cations and pyrazolium cations.
  • the anions of the ionic liquids may be e.g. to be anions from the groups listed below:
  • R a is a C 1 to C 12 alkyl group or a C 5 to C 12 aryl group, preferably a C 1 -C 6 alkyl group or a C 6 aryl group (tosylate), the alkyl sulfonates
  • R a is a C 1 to C 12 alkyl group, preferably a C 1 -C 6 alkyl group, the halides, in particular chloride, bromide or iodide, and the pseudohalides, such as thiocyanate and dicyanamide (formula: NC - N - CN -) of the carboxylates R a COO -;
  • R represents a C 1 to C 20 alkyl group or a C 6 to C 10 aryl or aralkyl group, preferably a C 1 -C 8 alkyl group, in particular acetate, the phosphates,
  • dialkyl phosphates of the formula Ra RbPC wherein R a and R b independently of one another represent a C 1 to C 6 alkyl group;
  • R a and Rb are the same alkyl group, which may be mentioned dimethyl phosphate and diethyl phosphate and the phosphonates, in particular the monoalkylphosphonic
  • R a RbPC “3 " wherein R a and Rb independently represent a C1 to C6 alkyl group.
  • Particularly preferred anions are methanesulfonate, trifluoromethanesulfonate, dimethyl phosphate, diethyl phosphate, methylsulfate, ethylsulfate, thiocyanate and dicyanamide as the anion in the ionic liquids.
  • the solvent is an imidazolium salt of the next formula I,
  • R 1 is an organic radical having 1 to 20 C atoms
  • R2, R4, R3 and R5 stand for an H atom or an organic radical having 1 to 20 C atoms, X stands for an anion and
  • n 1, 2 or 3.
  • R 1 and R 3 are preferably, independently of one another, an organic radical having 1 to 10 C atoms.
  • R 1 and R 3 are an aliphatic radical, in particular an aliphatic radical without further heteroatoms, for example an alkyl group.
  • Particular preference is given to R1 and R3 independently of one another for a C1 to C10 or. a C1 to C4 alkyl group.
  • R 1 and R 3 independently of one another are a methyl or an ethyl group.
  • R 2, R 4 and R 5 are preferably independently an H atom or an organic radical having 1 to 10 C atoms; in particular, R 2, R 4 and R 5 represent an H atom or an aliphatic radical. Particularly preferably, R 2, R 4 and R 5 independently of one another are an H atom or an alkyl group, in particular R 2, R 4 and R 5 independently of one another are an H atom or a C1 to C4 alkyl group. Most preferably, R2, R4 and R5 are each an H atom. n is preferably 1.
  • X is preferably one of the abovementioned and preferred anions, most preferably thiocyanate and dicyanamide.
  • ionic liquids e.g.
  • imidazolium salts having more carbon atoms in the substituents R1 to R5 may be advantageous because of better solubility.
  • imidazolium salts of the formula I are therefore used for such coating compositions in which the sum of all C atoms in the substituents R 1 to R 5 is at least 6, preferably 6 to 20; the substituents can be H atoms and e.g. Be alkyl groups, as stated above.
  • hydrophobic anions may also be used, e.g. Anions with a phenyl group, a heterocyclic group or a long-chain alkyl group.
  • R1 butyl
  • R3 butyl
  • R2 ethyl
  • R4 H
  • R5 H (number of C atoms in R1 to R5 in total
  • R1 ethyl
  • R3 methyl
  • R2 octyl
  • R4 H
  • R5 H (number of C atoms in R1 to R5 total 1 1).
  • phenylcarboxylate as the hydrophobic anion.
  • the intrinsic color of the ionic liquids which are contained in the organic fillers are typically preferred (eg clearcoat).
  • the ionic liquids have an iodine color number (according to DIN 6162) smaller than 20, particularly preferably smaller 15, very particularly preferably less than 10, in particular less than 5 and in a particular embodiment less than 1.
  • the organic fillers preferably contain at least 1% by weight, more preferably at least 3% by weight, most preferably at least 5% by weight and in a particular embodiment at least 10% by weight of ionic liquid.
  • the content of ionic liquid in the organic fillers is not higher than 40% by weight, especially not higher than 30% by weight. Due to the good antistatic effect, a content of not more than 20% by weight of ionic liquid in the organic fillers is sufficient.
  • the organic fillers may contain other ingredients in addition to the organic polymer and the ionic liquid.
  • Stabilizers desiccants, residual solvents from manufacturing process
  • inorganic fillers such as metal oxides, silicates or metal sulfates, pigments, dyes, flame retardants, thickeners, thixotropic agents, surface-active agents, plasticizers, chelating agents or other antistatic compounds.
  • antistatic compounds e.g. B: carbon in all its modifications, e.g. However, as carbon black, graphite or as carbon fiber, or metal or metal oxides are not required for a good antistatic finish and are therefore preferably at most in minor amounts of less than 5 wt.%, In particular less than 1 wt.%, Based on the total weight of the organic Fillers used. Most preferably, no other antistatic additives are used in the organic fillers. In particular, little or no antistatic additives containing metals are preferably used.
  • the organic fillers contain a total of less than 3 wt.%, In particular less than 0.5 wt.% Of metals, more preferably less than 0.1 wt.% Of metals; wherein the term "metals" includes metals in any form, that is, as an element, as a cation or as a component of complex compounds.
  • Suitable stabilizers include e.g. hindered phenols, secondary antioxidants such as phosphites, phosphonites, phosphonates and thioethers.
  • the organic fillers may include stabilizers e.g. in an amount of 0.05 to 5, particularly preferably from 0.1 to 3 wt.% Contain.
  • the above components may be brought into contact and mixed together in any order.
  • the ionic liquid and other constituents may already be present in the preparation of the organic polymer or added to the organic polymer only after the preparation and mixed with the polymer by conventional methods.
  • the ionic liquid may be added to the polymer, for example during thermoplastic processing, in particular, the ionic liquid may be added in the extrusion of the polymer.
  • the extrudate then contains the ionic liquid and, if desired, can be further processed, for example ground to a powder.
  • the polymer is used in the form of a powder.
  • the polymer or the mixture of polymer, ionic liquid and optionally other constituents is ground.
  • the powder has a particle size distribution with a dso value of 5 to 500 ⁇ m, in particular 10 to 400 ⁇ m, and a dgo value of 10 to 700 ⁇ m, in particular 20 to 500 ⁇ m.
  • powders having a dso value of 5 to 50 ⁇ , or a dgo value of 10 to 100 ⁇ are particularly suitable.
  • powders with a d 50 value of 50 to 400 ⁇ m, or a d 10 value of 100 to 700 ⁇ m are particularly suitable.
  • the dso value of the particle size distribution indicates that 50% by weight of the particles have a smaller diameter than the indicated diameter.
  • the dgo value of the particle size distribution indicates that 90% by weight of the particles have a smaller diameter than the indicated diameter.
  • the organic filler is obtained by milling the polymer into a powder and subsequently treating the powder with ionic liquid.
  • the polymer is harder without a content of ionic liquid and can therefore be ground more easily.
  • the polymer may be dried before adding the ionic liquid to the polymer.
  • the polymer powder preferably has a residual content of solvent (water or organic solvent) of less than 5% by weight, in particular less than 1% by weight, particularly preferably less than 0.2% by weight.
  • Ionic liquid is then added in the desired amount to the ground powder.
  • the powder absorbs the ionic liquid in sufficient quantities.
  • the polymer and the ionic liquid can be brought into contact in mixing equipment, for example in high-speed mixers.
  • the uptake of the ionic liquid by the polymer is assisted by a good mixing and takes place quickly and completely.
  • the ionic liquid can also be used in admixture with solvents.
  • solvents are understood in this patent application at 20 ° C liquid, non-ionic compounds, which are removed at the latest when using the coating or sealant.
  • the concomitant use of solvents may favor the uptake of the ionic liquid by the organic polymer and the distribution of the ionic liquid in the organic polymer.
  • Possible solvents are e.g. Water, alcohols, esters, ethers, ketones, aromatic solvents, alkoxylated Alkanklarealkylester, carbonates, respectively mixtures of the solvents.
  • Alcohols here are hydrocarbon compounds having one to three hydroxyl groups and a molecular weight of less than 200 g / mol.
  • Esters include, for example, n-butyl acetate, ethyl acetate, 1-methoxypropyl acetate-2 and 2-methoxyethyl acetate.
  • Ethers are, for example, THF, dioxane and the dimethyl, ethyl or n-butyl ethers of ethylene glycol, diethylene glycol, triethylene glycol, propylene glycol, dipropylene glycol or tripropylene glycol.
  • ketones are acetone, ethyl methyl ketone, diethyl ketone, isobutyl methyl ketone, methyl amyl ketone and tert-butyl methyl ketone. Acetone is less preferred because of its flash point.
  • aromatic hydrocarbons are xylene and toluene, in particular xylene.
  • Aromatic mixtures are in principle also suitable, but less preferred. Examples include the Solvesso® brands of ExxonMobil Chemical, especially Solvesso® 100 (CAS No. 64742-95-6, predominantly C 9 and Cio-aromatics, boiling range about 154-178 ° C), 150 (boiling range about 182 - 207 ° C) and 200 (CAS No. 64742-94-5), as well as the Shellsol® brands from Shell, Caromax® (eg Caromax® 18) from Petrochem Carless and Hydrosol from DHC (eg as Hydrosol ® A 170).
  • Solvesso® brands of ExxonMobil Chemical especially Solvesso® 100 (CAS No. 64742-95-6, predominantly C 9 and Cio-aromatics, boiling range about 154-178 ° C), 150 (boiling range about 182 - 207 ° C) and 200 (CAS No.
  • solvents are butylglycol diacetate, butylglycol acetate, dipropylene glycol dimethyl ether, 3-methoxy-n-butyl acetate, dipropylene glycol n-butyl ether and propylene carbonate.
  • Particularly preferred solvents are alcohols, such as methanol, ethanol, isopropanol, acetonitrile and mixtures thereof.
  • the solvents used for the ionic liquids are preferably those in which the ionic liquids used in each case dissolve at 23 ° C. to more than 10% by weight, preferably to more than 30% by weight.
  • the above co-use of solvent is generally not necessary when using mixing equipment as described above. However, it might be helpful if ionic liquid and polymer are brought into contact without mixing.
  • solvents can be separated from the powder, e.g. by heating.
  • the content of solvents in the powder is therefore preferably less than 5% by weight, more preferably less than 1% by weight and most preferably less than 0.3% by weight.
  • the ionic liquids are brought into the organic polymer without the use of solvents, the powders containing the ionic liquid are therefore preferably free of solvents.
  • organic fillers described above preferably consist overall of
  • the organic fillers are particularly preferably made
  • the organic fillers consist of 60 to 90 wt.
  • the organic polymer consist of 60 to 90 wt.
  • the organic fillers are used as additives for coating or sealing compounds.
  • Suitable coating or sealing compounds are those of any desired chemical composition and of any intended use.
  • the coating compositions may be, for example, adhesives, lacquers, paints, paper coating slips or floor coating compositions.
  • Sealants are generally also compositions with sticky properties, but which contain a high proportion of fillers such as calcium carbonate, titanium dioxide, silicates and are thus incorporated in high layer thicknesses in joints, cracks, crevices in order to seal them.
  • adhesives are e.g. Pressure-sensitive adhesives, contact adhesives or construction adhesives into consideration. Such adhesives are applied to at least one of the parts to be bonded as a coating composition in the desired layer thicknesses and then bonded by conventional methods.
  • coating materials such as lacquers, paints, paper coating slips or floor coating compositions protect, for example, against mechanical stress and / or have decorative purposes. They are suitable for coating substrates such as wood, wood veneer, paper, cardboard, textile, foil, leather, fleece, plastic surfaces, glass, ceramics, mineral building materials, such as cement blocks and fiber cement boards or metals, which are each optionally precoated or can be pretreated.
  • Such coating compositions are suitable as or in inner or outer coatings, ie those applications that are exposed to daylight, preferably of building parts, coatings on (large) vehicles and aircraft and industrial applications, commercial vehicles in the agricultural and construction sector, paint finishes, bridges, buildings Electricity pylons, tanks, containers, pipelines, power plants, chemical plants, ships, cranes, piles, sheet piling, fittings, pipes, fittings, flanges, couplings, halls, roofs and structural steel, furniture, windows, doors, parquet, can Coating and coil coating, for floor coverings, such as in department stores, in industrial plants, at parking decks or in hospitals.
  • the coating or sealing compounds preferably contain at least one binder and optionally further additives which are customary for the respective use.
  • the binders may be polymers, e.g. are obtainable by free radical polymerization, by polycondensation or other Polyaddukt Struktur.
  • polymers which contain more than 50% by weight, in particular more than 70% by weight, of (meth) acrylic monomers, e.g. C1 - C10 alkyl (meth) acrylates (polyacrylates for short).
  • Polyacrylates, vinyl ester polymers and styrene-butadiene polymers are preferably prepared by aqueous emulsion polymerization and are therefore preferably present as a dispersion in water.
  • Polyurethanes for coating purposes are frequently prepared by reacting the starting materials in water or organic solvents and are therefore preferably present as an aqueous polyurethane dispersion or as a solution of polyurethanes in an organic solvent.
  • Polyesters can e.g. are obtained by polycondensation in water or an organic solvent and are therefore preferably present as solutions.
  • Suitable binders are also oligomers or monomers which are preferably liquid at room temperature (20 ° C.) and require no solvent; these are, in particular, reactive binders in which a chemical reaction takes place after the coating or UV-curable binders which are cured after the coating by irradiation with UV light.
  • binder systems of two components are also used for coatings; these contain two different constituents which cure in use and are therefore referred to hereinafter as reactive binder systems.
  • reactive binder systems are mentioned e.g. Epoxy compounds and hardeners, preferably amine hardeners, which cure to epoxy resins.
  • Reactive binder systems called its compounds having at least two isocyanate groups (diisocyanates) and compounds having at least two hydroxyl groups (diols) which cure to form polyurethanes.
  • reactive binder systems compounds having at least two isocyanate groups (preferably diisocyanates) and compounds having at least two amino groups (preferably diamines) which cure to form polyureas.
  • UV-curable binders are (meth) acrylic monomers having more than one (meth) acrylic group, in particular aliphatic compounds having 2 to 5 (meth) acrylic groups and one Molecular weight less than 300 g / mol (eg Laromere® BASF) or low molecular weight polyesters containing radiation-curable groups, eg by co-use of maleic acid as dicarboxylic acid.
  • further additives customary for the respective use are, for example, tackifying resins (tackifiers, eg rosins), in the case of the sealants, for example fillers and / or pigments, for example calcium carbonates, titanium dioxide, alumina, silica, silicates).
  • paints, paints or floor coatings for example, dyes, pigments and / or fillers).
  • additives for the above uses are thickeners, leveling agents, stabilizers, etc.
  • the coating or sealing compounds may be aqueous coating or sealing compounds or coating or sealing compounds containing organic solvents; It may also be coating or sealing compounds which contain little or no water or organic solvents, in particular less than 5% by weight, particularly preferably less than 2% by weight, of water and organic solvents.
  • the latter coating or sealing compounds are e.g. those which contain liquid binders (reactive or UV-curable binders, see above) or those from which water or organic solvents have already been removed and which are therefore present, for example. as a powder, e.g. Powder coatings.
  • the organic fillers are suitable as additives for coating or sealing compounds.
  • the organic fillers may be mixed in any manner with the other ingredients of the coating or sealants.
  • solvent is understood in this patent application as stated above at 20 ° C liquid, nonionic compounds, which are removed at the latest when using the coating or sealant and therefore will not be part of the resulting coating or seal.
  • solvents are water or nonionic, organic solvents.
  • the coating or sealing compounds preferably comprise at least 0.1% by weight, more preferably at least 1% by weight, most preferably at least 5% by weight, in a particular embodiment at least 10% by weight of the organic fillers.
  • the coating or sealing compounds generally contain no more than 40% by weight, in particular not more than 30% by weight of the organic fillers, since a higher content is not necessary for optimum antistatic properties.
  • the coating or sealing compounds can be processed in the usual way.
  • the coatings obtained may have, for example, layer thicknesses of from 5 ⁇ m to 30 mm, preferably from 10 ⁇ m to 20 mm. With the sealants, for example, cracks, gaps or joints can be sealed or bridged with large or small dimensions.
  • the organic fillers are used as additives in floor coating compositions.
  • the floor coating compositions preferably comprise from 5 to 40% by weight, particularly preferably from 10 to 30% by weight, of the organic fillers, based on the total weight of all constituents of the floor coating compositions, with the exception of water and organic solvents.
  • the soil layers thus obtained can also be transparent in particular.
  • the resulting floor coatings preferably have a layer thickness of 1 mm to 30 mm, more preferably from 2 mm to 20 mm, particularly preferably from 4 mm to 20 mm.
  • conductive fillers such as graphite, carbon black, metal oxides or fibers such as carbon fibers, which build up a conductive structure in the coating, have generally been required.
  • the conductive structure dissipates charges into the floor.
  • conductive fillers such as carbon black, graphite or carbon fiber, or metal or metal oxides are not required for good antistatic finish and therefore preferably at most in minor amounts of less than 5 wt.%, In particular less than 1 % By weight, particularly preferably less than 0.2% by weight, based on the total weight in which the coating or sealing compound (without solvent, see above) is contained; most preferably, the coating or sealing compounds are free of such conductive fillers.
  • the above statements apply in particular to floor coating compositions, since here the organic powders take over the task of conductive fillers and derive charges by forming a coherent structure in the floor.
  • the coating or sealing compounds have very good antistatic properties. The good antistatic properties are retained over a long time. A decrease of the antistatic properties with time is not or hardly noticeable.
  • the application technology see properties of the coating and sealing compounds are not or only slightly affected.
  • Polyamide 12 Orgasol 2002 ES 5 NAT 3 (Arkema)
  • Basionics VS03 ethylmethylimidazolium dicyanamide (BASF SE)
  • Basionics FS 01 quaternary ammonium salt (BASF SE)
  • Basionics UV43 tripropyl allyl ammonium dicyanamide (BASF SE)
  • Filler 1 and 2 The commercially available polyamide 6 granules are comminuted with a successively connected mill combination of universal rotor mill and counterjet mill. Classification is done by screening. Coarse material is returned and ground again. A dry free-flowing powder is obtained (filler 1). To evaluate a polymer change in the extruder, the polyamide 6 is driven without additives through an extruder; the heating zones are 160-220 ° C in six stages and then ground in the same way as filler 1 (filler 2).
  • Polyamide 6 is introduced into a twin-screw extruder.
  • the heating zones are 160-220 ° C in six stages.
  • the ionic liquid is introduced via a separate metering.
  • the melt discharge is cooled in a water bath and chopped.
  • the polymer is dried to a water content ⁇ 0.1%.
  • the conductive granules are crushed in stages in a liquid nitrogen cooled air jet mill.
  • Filler 9 - Filler 1 1 Ionic liquid and isopropanol are mixed at 23 ° C. and ground polyamide 6 (see above, filler 1) is added thereto and heated to 60 ° C.
  • the ionic liquid is absorbed within 1 hour by the polyamide 6, the polyamide powder does not swell. Finally, the solvent is distilled off in vacuo in 30 minutes, leaving a dry free-flowing powder.
  • the commercially available polyamide 12 is used as supplied (filler 12).
  • Ionic liquid and isopropanol are mixed at 23 ° C and ground polyamide 12 (see above, filler 12) added thereto and heated to 60 ° C.
  • the ionic liquid is absorbed within 1 hour by the polyamide 12, the polyamide powder does not swell. Finally, the solvent is distilled off in vacuo in 30 minutes, leaving a dry free-flowing powder.
  • the Shore hardness D is a measure of the hardness. The higher the specified value of the Shore hardness, the greater the resistance of the tested material to the penetration of a measuring tip.
  • the glass transition temperature was determined by DSC (Differnetial Scanning Caolrimetry).
  • the volume resistivity (p) in [Qcrn] is the electrical resistance measured between the bottom of a floor covering and a single electrode located on the effective area, based on the thickness of the floor covering.
  • the surface resistivity [ ⁇ ] is the resistance between two points measured with two electrodes mounted on the effective area, based on the distance of the electrodes.
  • BVG Body Voltage Generation
  • the system resistance is the earth leakage resistance of the person / shoe / flooring system and is measured in accordance with EN 61340-4-5.
  • the system resistance should preferably be less than 35 megohms.
  • filler 6 was added to the above coating composition.
  • the amount of the organic filler added in each case refers to the coating obtained (without water or organic solvents which evaporate on drying). Filler 6 was readily miscible with the coating composition, a possible sediment could easily be stirred up even after prolonged storage of the resulting coating compositions.
  • This coating composition was prepared by the usual method and applied with a box wiper on a glass plate. After drying at 23 ° C over a period of 3 weeks, a dry paint film is obtained with a dry layer of 150-250 ⁇ .
  • Table 2 Coating compound 1
  • Coating compound 2 100% epoxy industrial floor coating
  • filler 1 1 was first mixed with the epoxy binder, the glycidyl ether and the inorganic fillers and then added to the hardener. The mixture was then coated on fiber cement board.
  • the resulting bottom coating had a layer thickness of about 2 mm.
  • the amount of the filler of the invention in the bottom coating was 22 wt.%.
  • filler 1 1 was replaced by filler 1 (without loading with ionic liquid) in the same amount.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Paints Or Removers (AREA)
  • Sealing Material Composition (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Adhesives Or Adhesive Processes (AREA)
EP14726627.4A 2013-06-10 2014-05-28 Beschichtungsmassen, enthaltend leitfähige füllstoffe Withdrawn EP3008139A1 (de)

Priority Applications (1)

Application Number Priority Date Filing Date Title
EP14726627.4A EP3008139A1 (de) 2013-06-10 2014-05-28 Beschichtungsmassen, enthaltend leitfähige füllstoffe

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP13171239 2013-06-10
EP14726627.4A EP3008139A1 (de) 2013-06-10 2014-05-28 Beschichtungsmassen, enthaltend leitfähige füllstoffe
PCT/EP2014/061058 WO2014198539A1 (de) 2013-06-10 2014-05-28 Beschichtungsmassen, enthaltend leitfähige füllstoffe

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DE102015211632A1 (de) 2015-06-23 2016-12-29 Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. Polymerzusammensetzung mit verzögertem Kristallisationsverhalten, das Kristallisationsverhalten beeinflussende Additivzusammensetzung, Verfahren zur Herabsetzung des Kristallisationspunktes sowie Verwendung einer Additivzusammensetzung
CN107686694A (zh) * 2017-05-27 2018-02-13 太仓卡斯特姆新材料有限公司 一种聚氨酯导静电漆及其制备方法
CN107629634A (zh) * 2017-10-26 2018-01-26 浙江华彩新材料有限公司 一种可直接回收的粉末涂料的制备方法
US20220061429A1 (en) * 2020-08-27 2022-03-03 The Fix Marketing, LLC Gaming gloves

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WO2007090755A1 (de) * 2006-02-07 2007-08-16 Basf Aktiengesellschaft Antistatisches polyurethan
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WO2007090755A1 (de) * 2006-02-07 2007-08-16 Basf Aktiengesellschaft Antistatisches polyurethan
WO2012029155A1 (ja) * 2010-09-02 2012-03-08 リケンテクノス株式会社 床材用塗料および床材
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JP2016528311A (ja) 2016-09-15
US20160130448A1 (en) 2016-05-12
WO2014198539A1 (de) 2014-12-18

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