EP2408866A1 - Beschichtungen unter einsatz von dialkyl-/dialkenylethern als hydrophobierungsmittel, deren verwendung und metalle versehen mit der beschichtung - Google Patents

Beschichtungen unter einsatz von dialkyl-/dialkenylethern als hydrophobierungsmittel, deren verwendung und metalle versehen mit der beschichtung

Info

Publication number
EP2408866A1
EP2408866A1 EP10717494A EP10717494A EP2408866A1 EP 2408866 A1 EP2408866 A1 EP 2408866A1 EP 10717494 A EP10717494 A EP 10717494A EP 10717494 A EP10717494 A EP 10717494A EP 2408866 A1 EP2408866 A1 EP 2408866A1
Authority
EP
European Patent Office
Prior art keywords
coating
ethers
dialkyl
coating according
ether
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Withdrawn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
EP10717494A
Other languages
German (de)
English (en)
French (fr)
Inventor
Oliver Herzog
Boie Witt
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.)
Sasol Germany GmbH
Original Assignee
Sasol Germany GmbH
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 Sasol Germany GmbH filed Critical Sasol Germany GmbH
Publication of EP2408866A1 publication Critical patent/EP2408866A1/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Withdrawn legal-status Critical Current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
    • C09D5/36—Pearl essence, e.g. coatings containing platelet-like pigments for pearl lustre
    • 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
    • C09D5/008—Temporary coatings
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/26—Web or sheet containing structurally defined element or component, the element or component having a specified physical dimension

Definitions

  • the invention relates to coatings of surfaces using dialkyl / dialkenyl ethers, in particular for the purposes of hydrophobic finishing of surfaces, metals provided with such a coating, including .metal compounds or alloys, and the use of the coatings as surface protection.
  • a water-repellent effect of surfaces can be achieved if they are provided hydrophobic and / or the surface structures are suitably modified. In nature, this occurs, for example, in the leaf of the lotus flower, which shows an extremely high water repellency. Responsible for this is a complex micro- and nanoscopic architecture of the surface. The aim of many developments was and is to make this property usable in commercial products.
  • silicone oils and polymers are used to permanently apply powders of kaolin, talc, clay or silica gel to surfaces which, if appropriately equipped, should have a lotus leaf-like water repellency.
  • EP 0909747 A1 teaches to build up hydrophobic surfaces by applying a dispersion of powder particles from an inert material in a hydrophobicizing siloxane solution with subsequent curing, which have elevations in the order of magnitude of 5 to 200 ⁇ m.
  • WO 00/58410 and WO 96/04123 describe self-cleaning surfaces obtainable by applying a liquid containing a hydrophobic material, wherein the hydrophobic material "self-organizing" after evaporation provides a surface structure with mountains and valleys that are a distance of 0.1 to 200 and hydrophobic material are waxes (WO 00/58410), for example long-chain alkanes, alcohols, in particular diols, and ketones, in particular diketones, or polymers (WO 96/04123) called , Many known from the prior art materials with low surface free energy, such as silicones or perfluoro compounds, have an undesirable, because the further processability of the workpieces influencing effect.
  • the object of the present invention was to develop a process for the hydrophobic treatment of surfaces, in particular for temporary hydrophobization, the coating of which can be removed by commercially available cleaning agents and whose further processing, such as overcoating or melting, is unproblematic.
  • the coating of surfaces with dialkyl / dialkenyl ethers is extensive and leads to an advantageous hydrophobizing finish of the surface, which is easily removable and can also have a pearlescent effect.
  • Linear dialkyl / dialkenyl ethers have low surface tensions in the range around 30 mN / m and can nevertheless be easily and extensively removed from surfaces with commercially available cleaners.
  • An example of this are conformal coatings, e.g. Car polishes.
  • Dialkyl / dialkenyl ethers are not attacked by water, only in conjunction with appropriate cleaners can be removed.
  • so-equipped surfaces have the advantage of being readily wettable by many organic materials.
  • silicone oil-containing products with a hydrophobic effect can not be removed or not completely removed.
  • a further advantage of the dialkyl / dialkenyl ethers used according to the invention lies in the good environmental compatibility of these materials in contrast to the silicone oils or perfluorocompounds.
  • the dialkyl / dialkenyl ethers form on the surface of the coated material a film which has a higher water repellency due to its micro-roughness than investigated comparative products from the family of alcohols, paraffins and
  • the hydrophobic material can be applied in solid state, as a solution, in dispersion or emulsion.
  • the hydrophobic material is applied as a solid either in powder form or as a melt. As the melt cools, the hydrophobic layer forms. Due to the excellent spreading properties of the dialkyl ethers in liquid form, they are evenly distributed in a thin layer on the material.
  • the powder may be a micronized solid applied to the surface or a regrind of coarser more heterogeneous particle size distribution.
  • Suitable water-repellent dialkyl / dialkylene ethers are those of the general empirical formula R 1 -O-R 2 , where R 1 and R 2 may be saturated or unsaturated alkyl / alkylene chains having chain lengths of 1 and more carbon atoms, as long as the dialkyl / dialkylene ethers in the sum have more than 18 carbon atoms.
  • the dialkyl / Dialkylenether can according to an embodiment of the invention, together with additives which form part of the coating, such as. B.
  • C14 to C36 fatty alcohols in particular linear C14 to C36 fatty alcohols, are used, with 1-alkanols such as 1-tetradecanol, 1-
  • Pentadecanol 1-hexadecanol, 1-heptadecanol, 1-octadecanol, 1-nonadecanol, 1-eicosanol, 1-heneicosanol, 1-docosanol, 1-tricosanol, 1-tetracosanol, 1-pentacosanol, 1-hexacosanol, 1-heptacosanol, 1-octacosanol, 1-nonacosanol or 1-triacontanol are preferred.
  • C14 to C32 carboxylic acids in particular fatty acids or linear mono-1-carboxylic acids such as 1-decanoic acid, 1-undecanoic acid, 1-dodecanoic acid, 1-tridecanoic acid , 1-tetradecanoic acid, 1-pentadecanoic acid, 1-hexadecanoic acid, 1-heptadecanoic acid, 1-octadecanoic acid, 1-nonadecanoic acid, 1-eicosanoic acid, 1-heneicosanoic acid, 1-docosansaneu, 1 Tricosanoic acid, 1-tetracosanoic acid, 1-pentacosanoic acid, 1-hexacosanoic acid, 1-heptacosanoic acid, 1-octacosanoic acid, 1-nonacanoic acid, 1-tricontanoic acid.
  • fatty acids or linear mono-1-carboxylic acids such as 1-decanoic acid, 1-und
  • the proportion of the above additives in the coating is preferably (together) 5 to 40% by weight, in particular 7 to 30% by weight.
  • additives can be used, for example, to increase the adhesion to the surface without adversely affecting the hydrophobic properties.
  • Possible fields of application of the hydrophobizing agents according to the invention include, but are not limited to: garments, awnings, paints, for example car paints, building walls or leather goods.
  • inorganic particles in particular from 0.5 to less than 5% by weight, may be incorporated into the coating, for example those having average particle diameters D 5 o, determined in accordance with ISO 13320-1 and evaluated according to the Fraunhofer Theory of less than 50 .mu.m, in particular particulate metal oxides, mischmetal oxides and / or their oxide hydrates, such as silica, kieselguhr, china clay, or alumina particles.
  • FIG. 1 The invention is illustrated by FIG. 1 and the following examples, without being limited thereto.
  • the coating composition was melted at a temperature of at least 5 ° C. above its melting point.
  • the body to be coated such as a glass slide, dipped and quickly pulled out again.
  • layer thicknesses in the range of 50 microns - 500 microns, wherein the layer thickness depends inter alia on the temperature of the object and the speed of extraction.
  • the coating agent was ground with a coffee grinder to a fine powder.
  • the powder On the surface of the object to be coated, e.g. a glass slide, the powder was evenly distributed. Subsequently, the object was tempered at a temperature of at least 5 ° C. above the melting point in an oven for 10 minutes and then cooled, whereby the coating forms. In this way, layer thicknesses of 10 microns to 500 microns were achieved.
  • the contact angles were measured using a contact angle measuring device DSA100 from Krüss.
  • DSA100 from Krüss.
  • the coated surface was wetted with a drop of water.
  • the drop was illuminated from one side and recorded on the opposite side by a camera.
  • the resulting film was evaluated using the DSA 100 software.
  • the arithmetic mean was determined from 100 measuring points, where 1 measuring point is the arithmetic mean of the contact angles of the hanger and the right drop contour.
  • the layer thickness of the uncoated object e.g., a glass slide
  • the layer thickness of the uncoated object was measured by means of a film thickness gauge at 10 different defined locations. After the application process, the measurement was repeated and determined from the difference, the layer thickness.
  • Dioctadecylether available for example under the name ® NACOL ether 18 from Sasol Germany GmbH, was applied from the melt to a desired surface. Upon cooling, the ether showed an opalescent effect. As a result of the coating, the surface became hydrophobic and thus protected from water. On the material thus treated, a contact angle of water of 148 ° was measured.
  • Dioctadecylether available for example as NACOL ® ether 18 from Sasol Germany GmbH, was finely ground and applied as a powder uniformly to a desired surface. After annealing at 80 0 C the contact angle of water on the surface is determined to be 148 °. A pearlescent effect is observed.
  • Example 3 Dihexadecylether, available for example as NACOL ® ether 16 from Sasol Germany GmbH, was finely ground and applied as a powder uniformly to a desired surface. After annealing at 80 0 C the contact angle of water was determined on the surface to 141 °.
  • Dihexadecylether available for example as NACOL ® ether 16 from Sasol Germany GmbH, was applied from the melt to a desired surface.
  • Didocosyl ether was applied from the melt to any surface. After annealing at 80 0 C the contact angle of water was determined on the surface to 144 °.
  • Didocosyl ether was finely ground and applied as a powder evenly on any surface. After annealing at 80 0 C the contact angle of water was determined on the surface to 144 °. A pearlescent effect was observed.
  • Dioctadecylether available for example as NACOL ® Ether 18 from Sasol Germany GmbH, was wearing listed in acetone on any surface as a 20% solution. After evaporation of the solvent, the contact angle of water on the surface was determined to be 156 °.
  • 1-octadecanol obtainable for example under the name NACOL ® 18-98 by Sasol Germany GmbH, was sticking aside- from the melt to any surface. After cooling, a contact angle of water on the wax layer of 101 ° was found.
  • 1-octadecanol available for example under the name ® NACOL 18-98 by Sasol Germany GmbH, was applied in acetone to any surface as a 20% solution. After evaporation of the solvent, the contact angle of water on the surface is measured to be 112 °.
  • Comparative Example 4 octadecane, available for example under the name ® Parafol 18-97 by Sasol Germany GmbH, was applied from the melt to a desired surface. After cooling, a contact angle of water on the wax layer of 111 ° is found.
  • Montan wax is applied with a dropping point of 82 ° C and an acid number of 144 mg KOH / g (Licowax S ® ex. Clariant), was prepared from the melt to a desired surface. After cooling, a contact angle of water on the wax layer of 111 ° is found.
  • Example 11 The contact angle of water on a glass slide was determined to be 11 °. Subsequently, this is coated in the melt with Dioctadecylether. The contact angle of the surface is now 148 °. Part of the coating was removed mechanically, where the contact angle of water with the surface was measured. He was 12 °. Another part of the coating was treated with a 60 0 C warm 10% commercial detergent solution (Palmolive ® , Colgate GmbH) in water and rinsed the surface with deionized water. A new measurement of the contact angle of water with the surface also gave 12 °.
  • the contact angle of water on a glass slide was determined to be 11 °. This is treated with a silicone oil (Dow Corning 200). Thereafter, the contact angle of the water droplet with the surface was measured to be 91 °. The silicone oil was removed mechanically by wiping. Water had a contact angle of 56 ° on the cleaned surface. Thereafter, the slide was treated with a 10% commercial detergent solution (Palmolive ® , Colgate GmbH) in water at 60 0 C and rinsed the surface with deionized water. A new measurement resulted in a contact angle of 39 °.
  • Examples 11 and V8 show that it is possible to use the coating of the invention by suitable means, e.g. mechanical or chemical, residue-free removal. For coating with silicone oils, this is not possible without the surface being further hydrophobicized.
  • an emulsion was prepared. This was 1, 7 wt.% Of a mixture of Marlinat® 242 / 90M (mono-isopropanol ammonium salt of a linear C12-C14 alcohol polyethylene glycol ether (2EO) sulphates), 0.7 wt.% Of a Cetearylethoxylates (25 EO) and 3 , 5% by weight of demineralized water and heated to 65 ° C. To this was added a mixture of 35.3% by weight of the dioctadecyl ether mixture heated to 65 ° C (e.g., 80:20 according to Example A2).
  • Example A12 Significant performance improvement can be seen by using the wax paste described in Example A12.
  • the commercial polishes VG A1- VG A4 already contain abrasives. Even without a grinding wheel, the polish from Example A12 gives better results. With the addition of 3% abrasive bodies (here Aerosil 300), the result could be significantly improved (see Example A12).
  • the contact angle of white oil Merkur WOP 100 WB on the surface was determined on the coated surfaces according to the aforementioned examples. At the same time, the dissolution of the coating and the spreading of the oil drop are evaluated after 1 h and after 24 h.
  • Example contact angle solver l the spreading of the ⁇ coating after oil drop after
  • Examples 1, 5 and 8 have both an improvement in oil repellency, measured by the contact angle, as well as a comparable spreading behavior after 1 h and 24 h.
  • Example A8 is most suitable, for the coating of glass the mixture of Example 8.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Paints Or Removers (AREA)
  • Application Of Or Painting With Fluid Materials (AREA)
  • Materials Applied To Surfaces To Minimize Adherence Of Mist Or Water (AREA)
EP10717494A 2009-03-18 2010-03-15 Beschichtungen unter einsatz von dialkyl-/dialkenylethern als hydrophobierungsmittel, deren verwendung und metalle versehen mit der beschichtung Withdrawn EP2408866A1 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE102009013315A DE102009013315A1 (de) 2009-03-18 2009-03-18 Beschichtungen unter Einsatz von Dialkyl-/Dialkenylethern als Hydrophobierungsmittel, deren Verwendung und Metalle versehen mit der Beschichtung
PCT/DE2010/000277 WO2010105599A1 (de) 2009-03-18 2010-03-15 Beschichtungen unter einsatz von dialkyl-/dialkenylethern als hydrophobierungsmittel, deren verwendung und metalle versehen mit der beschichtung

Publications (1)

Publication Number Publication Date
EP2408866A1 true EP2408866A1 (de) 2012-01-25

Family

ID=42244881

Family Applications (1)

Application Number Title Priority Date Filing Date
EP10717494A Withdrawn EP2408866A1 (de) 2009-03-18 2010-03-15 Beschichtungen unter einsatz von dialkyl-/dialkenylethern als hydrophobierungsmittel, deren verwendung und metalle versehen mit der beschichtung

Country Status (6)

Country Link
US (1) US20120094110A1 (ja)
EP (1) EP2408866A1 (ja)
JP (1) JP5864407B2 (ja)
CN (1) CN102356132B (ja)
DE (1) DE102009013315A1 (ja)
WO (1) WO2010105599A1 (ja)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2480613B1 (de) * 2009-09-23 2018-10-31 SASOL Germany GmbH Zusammensetzungen enthaltend dialkylether, daraus hergestellte beschichtungen und verwendung von dialkylethern

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7005557B2 (en) * 2001-07-03 2006-02-28 The Procter & Gamble Company Film-forming compositions for protecting skin from body fluids and articles made therefrom
US20080292802A1 (en) * 2005-06-09 2008-11-27 Hironori Tonomura Method of Forming a Brilliant Multi-Layered Coating Film

Family Cites Families (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2011348A (en) * 1933-05-26 1935-08-13 Eastman Kodak Co Antistatic thin sheeting
CH268258A (fr) 1946-07-30 1950-08-16 Rhone Poulenc Chemicals Revêtement hydrofuge.
US2873202A (en) * 1956-02-23 1959-02-10 Johnson & Son Inc S C Water repellent and mar resistant coating composition containing a waxy dialkyl ether
GB913044A (en) * 1959-11-04 1962-12-12 British Sidac Ltd Improvements to coatings of vinylidene chloride copolymers
US3393081A (en) * 1966-12-06 1968-07-16 Monsanto Co Heat sealable moisture barrier coatings for polystyrene articles
GB8300773D0 (en) * 1983-01-12 1983-02-16 Ici Plc Coating compositions
JPS6013593A (ja) * 1983-07-02 1985-01-24 Dainippon Printing Co Ltd 感熱記録体
US4566907A (en) * 1984-02-14 1986-01-28 Mitsubishi Paper Mills, Ltd. Color-developing ink for non-carbon copying paper
DE4121147A1 (de) * 1991-06-26 1993-01-07 Henkel Kgaa Antischaummittel
CZ295850B6 (cs) 1994-07-29 2005-11-16 Wilhelm Prof. Dr. Barthlott Samočisticí povrchy předmětů, způsob jejich výroby a jejich použití
JPH0848942A (ja) * 1994-08-04 1996-02-20 Sofuto Kyukyu Corp:Kk 自動車の塗膜用撥水性艶出し剤
DE19602848A1 (de) * 1996-01-26 1997-07-31 Basf Ag Verfahren zur Herstellung von Pigmenten
WO1997035919A1 (fr) * 1996-03-22 1997-10-02 Nippon Zeon Co., Ltd. Liquide contenant un polymere lubrifiant et technique de formation d'une pellicule de polymere lubrifiant
DE69703770T2 (de) * 1996-08-14 2001-07-12 Tokyo Ohka Kogyo Co Ltd Besichtigungslösung auf Polysilazan-Basis für die Isolierung mit einer Zwischenschicht
DE19746053B4 (de) 1997-10-17 2006-11-16 Erlus Aktiengesellschaft Verfahren zur Erzeugung einer Selbstreinigungseigenschaft von Oberflächen, insbesondere an Dachziegeln, sowie keramischer Körper mit selbstreinigender Oberfläche
RU2246514C2 (ru) 1999-03-25 2005-02-20 Вильхельм БАРТЛОТТ Способ изготовления самоочищающихся поверхностей и изделие с такой поверхностью
WO2002046291A1 (en) * 2000-11-15 2002-06-13 Henkel Loctite Corporation Multi-functional alpha-alkoxyalkyl acrylate and methacrylate ester compositions and reworkable polymers formed therefrom
DE10137544A1 (de) * 2001-08-01 2003-02-13 Basf Ag Primerschichten für EC-Fenster
DE102005023804A1 (de) * 2005-05-19 2006-11-23 Basf Ag Farbiges Polymersystem mit verbesserter Elastizität
DE102008005721C5 (de) * 2008-01-23 2012-04-19 Sasol Germany Gmbh Verfahren zur Herstellung eines Latentwärmespeichermaterials
DE102009042447A1 (de) * 2009-09-23 2011-04-07 Sasol Germany Gmbh Zusammensetzungen enthaltend Dialkylether, daraus hergestellte Beschichtungen und Verwendung von Dialkylethern

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7005557B2 (en) * 2001-07-03 2006-02-28 The Procter & Gamble Company Film-forming compositions for protecting skin from body fluids and articles made therefrom
US20080292802A1 (en) * 2005-06-09 2008-11-27 Hironori Tonomura Method of Forming a Brilliant Multi-Layered Coating Film

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See also references of WO2010105599A1 *

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2480613B1 (de) * 2009-09-23 2018-10-31 SASOL Germany GmbH Zusammensetzungen enthaltend dialkylether, daraus hergestellte beschichtungen und verwendung von dialkylethern

Also Published As

Publication number Publication date
CN102356132A (zh) 2012-02-15
WO2010105599A1 (de) 2010-09-23
JP2012520903A (ja) 2012-09-10
DE102009013315A1 (de) 2010-09-23
US20120094110A1 (en) 2012-04-19
CN102356132B (zh) 2015-04-01
JP5864407B2 (ja) 2016-02-17

Similar Documents

Publication Publication Date Title
DE2458417C3 (ja)
EP2247701B1 (de) Verfahren zur beschichtung von metallischen oberflächen mit einer wachse enthaltenden schmierstoffzusammensetzung
EP1519994A1 (de) Verfahren zur herstellung einer tensidfreien suspension auf wässriger basis von nanostrukturierten, hydrophoben partikeln und deren verwendung
DE112009000066T5 (de) Zusammensetzung eines Antihaftlacks und Verfahren zur Herstellung derselben
WO2019105741A1 (de) Verfahren zur herstellung eines glasartikels
EP2888386B1 (de) Korrosionsschutzmittel-formulierung zum schutz vor zink- und cadmiumkorrosion
DE102008020216A1 (de) Verfahren zum Schützen eines Metalls vor Korrosion
DE69930601T2 (de) Molybdat-Pigmente enthaltende Pasten auf Basis von inhibierten Metallpigmenten zur Verwendung in wässrigen Beschichtungen
DE69627515T2 (de) Material zur verleihung von nicht-klebenden und nicht-benetzenden eigenschaften
DE2200654A1 (de) Pigment mit Korrosionsschutzeigenschaften,Verfahren zu seiner Herstellung und seine Verwendung
DE10305612B4 (de) Beschichtungsmassen für Gusskerne
EP2408866A1 (de) Beschichtungen unter einsatz von dialkyl-/dialkenylethern als hydrophobierungsmittel, deren verwendung und metalle versehen mit der beschichtung
WO2014146927A1 (de) Zusammensetzung für den schutz vor zunder und als schmiermittel für die heissverarbeitung von metallen
DE3223410C2 (de) Lösungsmittelhaltiger Lack mit Farbpigment
EP2217742A1 (de) Passivierendes gleitschleifen, insbesondere für aluminium, magnesium und zink
EP1862239B1 (de) Sprühkopf zum Auftragen von Trennmittel auf eine Gussform
WO2008037236A1 (de) Wärmehärtende beschichtungszusammensetzung
DE19716514C1 (de) Verfahren zum pulvermetallurgischen Herstellen und damit hergestellte Bauteile
DE2526930B2 (de) Trenn- und schmiermittel sowie verfahren zur herstellung eines schmierund trennueberzugs auf oberflaechen von formen und verwandten teilen
EP3921375B1 (de) Gleitmittel
WO2003046090A2 (de) Zubereitungen zur anti-fingerabdruck-beschichtung von metalloberflächen
DE202009008205U1 (de) Verwendung einer wachshaltigen Zusammensetzung als Beschichtung von Oberflächen zur Verbesserung ihrer Reinigbarkeit
CH694734A5 (de) Zusammensetzung zum Aufbringen auf Substrate, Verfahren zum Aufbringen derselben, ihre Verwendung sowie die aufgebrachten Strukturen.
DE1669099A1 (de) Schuppenfoermige Metallpulver sowie Verfahren und Mittel zu ihrer Herstellung
EP3102641A1 (de) Farben, lacke oder andere beschichtungsmittel mit anti-krater-additiv sowie dessen herstellung und verwendung

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 20110908

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO SE SI SK SM TR

DAX Request for extension of the european patent (deleted)
17Q First examination report despatched

Effective date: 20141114

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: EXAMINATION IS IN PROGRESS

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN

18D Application deemed to be withdrawn

Effective date: 20181002