Classifications

• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C217/00—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton
  • C07C217/02—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton
  • C07C217/04—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated
  • C07C217/06—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one etherified hydroxy group and one amino group bound to the carbon skeleton, which is not further substituted
  • C07C217/14—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one etherified hydroxy group and one amino group bound to the carbon skeleton, which is not further substituted the oxygen atom of the etherified hydroxy group being further bound to a carbon atom of a six-membered aromatic ring
  • C07C217/16—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one etherified hydroxy group and one amino group bound to the carbon skeleton, which is not further substituted the oxygen atom of the etherified hydroxy group being further bound to a carbon atom of a six-membered aromatic ring the six-membered aromatic ring or condensed ring system containing that ring not being further substituted
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C271/00—Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
  • C07C271/06—Esters of carbamic acids
  • C07C271/08—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms
  • C07C271/10—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms
  • C07C271/22—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms to carbon atoms of hydrocarbon radicals substituted by carboxyl groups
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C217/00—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton
  • C07C217/02—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton
  • C07C217/04—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated
  • C07C217/06—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one etherified hydroxy group and one amino group bound to the carbon skeleton, which is not further substituted
  • C07C217/14—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one etherified hydroxy group and one amino group bound to the carbon skeleton, which is not further substituted the oxygen atom of the etherified hydroxy group being further bound to a carbon atom of a six-membered aromatic ring
  • C07C217/18—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one etherified hydroxy group and one amino group bound to the carbon skeleton, which is not further substituted the oxygen atom of the etherified hydroxy group being further bound to a carbon atom of a six-membered aromatic ring the six-membered aromatic ring or condensed ring system containing that ring being further substituted
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C269/00—Preparation of derivatives of carbamic acid, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
  • C07C269/02—Preparation of derivatives of carbamic acid, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups from isocyanates with formation of carbamate groups
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
  • C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
  • C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
  • C08F220/10—Esters
  • C08F220/12—Esters of monohydric alcohols or phenols
  • C08F220/16—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms
  • C08F220/18—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms with acrylic or methacrylic acids
  • C08F220/1808—C8-(meth)acrylate, e.g. isooctyl (meth)acrylate or 2-ethylhexyl (meth)acrylate
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
  • C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
  • C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
  • C08F220/10—Esters
  • C08F220/22—Esters containing halogen
  • C08F220/24—Esters containing halogen containing perhaloalkyl radicals
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
  • C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
  • C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
  • C08F220/10—Esters
  • C08F220/34—Esters containing nitrogen, e.g. N,N-dimethylaminoethyl (meth)acrylate
  • C08F220/343—Esters containing nitrogen, e.g. N,N-dimethylaminoethyl (meth)acrylate in the form of urethane links
  • C08F220/346—Esters containing nitrogen, e.g. N,N-dimethylaminoethyl (meth)acrylate in the form of urethane links and further oxygen
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
  • C08F290/00—Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups
  • C08F290/02—Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups on to polymers modified by introduction of unsaturated end groups
  • C08F290/06—Polymers provided for in subclass C08G
  • C08F290/067—Polyurethanes; Polyureas
• • 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
  • C09D133/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Coating compositions based on derivatives of such polymers
  • C09D133/04—Homopolymers or copolymers of esters
  • C09D133/14—Homopolymers or copolymers of esters of esters containing halogen, nitrogen, sulfur or oxygen atoms in addition to the carboxy oxygen
  • C09D133/16—Homopolymers or copolymers of esters containing halogen atoms
• • 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
  • C09D4/00—Coating compositions, e.g. paints, varnishes or lacquers, based on organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond ; Coating compositions, based on monomers of macromolecular compounds of groups C09D183/00 - C09D183/16
  • C09D4/06—Organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond in combination with a macromolecular compound other than an unsaturated polymer of groups C09D159/00 - C09D187/00
• • 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
  • C09D5/16—Antifouling paints; Underwater paints
  • C09D5/1606—Antifouling paints; Underwater paints characterised by the anti-fouling agent
  • C09D5/1637—Macromolecular compounds
• • 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
  • C09D5/16—Antifouling paints; Underwater paints
  • C09D5/1681—Antifouling coatings characterised by surface structure, e.g. for roughness effect giving superhydrophobic coatings or Lotus effect
• • G—PHYSICS
  • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
  • G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
  • G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
  • G03F7/0002—Lithographic processes using patterning methods other than those involving the exposure to radiation, e.g. by stamping
• • G—PHYSICS
  • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
  • G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
  • G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
  • G03F7/16—Coating processes; Apparatus therefor
  • G03F7/161—Coating processes; Apparatus therefor using a previously coated surface, e.g. by stamping or by transfer lamination

Definitions

• the present invention relates to new oligomoric compounds based on hexafluoropropylene oxide (HFPO), compositions which contain these compounds, substrates whose surfaces have been modified with these compounds, and a process for the preparation and a use of the compounds.
• HFPO hexafluoropropylene oxide
• non-stick additives which are already in a mass fraction of less than 1% on UV-NIL-embossed
• NIL nano imprint lithography
• Nano-embossed lithography can bring about a lotus effect (cf. “The Lowest Surface Free Energy Based on -CF3 Alignment”, Takashi
• the lotus effect is based on a high proportion of CF3 groups, which have a much lower surface energy than -CF 2 groups.
• HFPO methacrylate 01igo-HFP0-2-hydroxyethyl methacrylate ester
• HFPO methacrylate can oxidize the -CH2-OH- alcohol group of an HFPO alcohol to form a carboxylic acid group and
• One object of the present invention is to provide a highly effective anti-stick additive and compositions (UV-NIL embossing lacquers) containing it.
• Another task is to provide a simple
• composition Composition, the polymer, the coated substrate, the method and the use according to the invention solved.
• the compound of the invention has a low
• the compound according to the invention can be prepared in a simpler manner and with a higher yield than HFPO methacrylate.
• the starting compounds which can be used for the synthesis of the compound according to the invention are simple and inexpensive to prepare.
• FIG. 1 shows schematically the formation of
• FIG. 2 shows the water and diiodomethane contact angle (CA) on an embossing lacquer layer of Example 1 which is UV-cured under protective gas as a function of the concentration of PFPE-UA-3.
• FIG. 3 shows the surface energy on an embossing lacquer layer of Example 1 which is UV-cured under protective gas as a function of the PFPE-UA-3 concentration.
• Figure 4 shows the water and diiodomethane contact angle on an embossing lacquer layer of Example 2 as a function of the
• FIG. 5 shows the surface energy on an embossing lacquer layer of Example 2 as a function of the PFPE-UA-3 concentration.
• the present invention provides a compound of formula (I):
• n is selected from 3 to 8 and R is hydrogen or a C 1 -C 5 alkyl radical. R is preferably hydrogen or the methyl radical.
• the polymerizable carbon-carbon double bond can preferably be organically polymerized under the action of light and / or heat and / or by chemical means. It is photochemical under the action of actinic radiation
• the polymerization reaction is usually a polyreaction in which the reactive double bonds or rings are converted into polymers under the influence of heat, light, ionizing radiation or chemically (via a redox reaction)
• the organic polymerization is preferably carried out via (meth) acrylic groups.
• the compound of the invention has a high level of CF3 residues.
• the compound according to the invention has a very regular structure, as a result of which an ordered and very densely packed fluorosurfactant layer structure is possible. This structure is reinforced by the possibility of training
• the compound of the present invention can be obtained by reacting an alcohol with an isocyanate. The difference to that
• HFPO methacrylate can be produced by oxidation of the -CH2-OH alcohol group of an HFPO alcohol to the carboxylic acid group and subsequent esterification with 2-hydroxyethyl methacrylate.
• a compound according to the invention is, for example, an oligo-urethane acrylate and can be produced, for example, by converting an oligo-HFPO alcohol into the urethane acrylate by addition to 2-isocyanatoethyl acrylate (AOI).
• AOI 2-isocyanatoethyl acrylate
• the oligomer used as the starting compound has units derived exclusively from propylene oxide, so that it can be produced in a simple manner.
• the urethane group present as a head group in the compounds according to the invention is polar due to an additional N atom and can also form H-bridge bonds through the H atom on the N atom. This leads to more highly ordered and more densely packed fluorosurfactant monolayers on the polymer surface and thus to lower ones
• composition of the invention contains the compound of the invention and a polymer starting material.
• Polymer starting material comprises monomers and / or oligomers with at least one reactive group which can be reacted with the carbon-carbon double bond in the compound according to the invention with polymerization.
• this is also a radical with a carbon-carbon double bond.
• groups containing double bonds are those which have double bonds accessible to Michael addition, such as styryls, norbornenyls or (meth) acrylic acid derivatives; but it can also be vinyl or allyl groups.
• (meth) acrylic derivatives and (meth) acrylic acid derivatives are above all the
• the polymer starting material can also comprise residues, the diamines or higher amines or dithiols or higher thiols
• Polymer starting material are selected so that a
• composition according to the invention contains the compound according to the invention in an amount of 0.001 to 10%, preferably 0.001 to 1.0%, and the polymer starting material in an amount of 50 to 99.999%.
• the remaining constituents can be, for example, a reactive diluent in a preferred amount of 5 to 40% and a photoinitiator. The percentages in the present
• a preferred composition contains 0.01 to 3% of the compound according to the invention, 50 to 80%
• Polymer starting material 5 to 30% reactive diluent and 0.1 to 3% photoinitiator, the total amount of these components being at least 90%, preferably at least 95% of the total amount of
• a polymer according to the invention is formed.
• This can be in any Form, e.g. B. in solid form as a film or in liquid form in a facade paint or a spray.
• the compound of the invention can be in the form of
• Composition according to the invention can be used to coat a substrate.
• a substrate can be any object whose surface is to be provided with the desired non-stick property.
• a substrate is therefore, for example, a substrate or carrier in a microstructure provided with embossing lacquer or a stamp for embossing such lacquers.
• any surface e.g. B. a glass surface can be used whose surface is to be designed to be dirt-repellent or self-cleaning.
• substrates are surfaces in the field of photovoltaics, lighting or optics, but also textiles, awnings, tarpaulins and sails that are self-cleaning or
• This coating creates a coating according to the invention
• coated substrate with the desired surface properties in particular a non-stick property and a modified one
• a coated substrate according to the invention can be, for example, a substrate which is coated with a polymer according to the invention as embossing lacquer, or a working stamp for the
• Nano-embossed lithography which is coated with a polymer according to the invention as a non-stick coating or in which the embossed structure or the embossed relief consists of this polymer according to the invention.
• a stamp can comprise a polymer substrate film (e.g. PET) with a structured surface layer which the polymer according to the invention has at least on its surface.
• the structured surface layer can be a polymer which can be obtained by UV curing an acrylate together with the compound according to the invention.
• both the embossing lacquer and the stamp surface have a compound according to the invention.
• connection between the substrate and the polymer according to the invention can be used are basically based on covalent or non-covalent bonds.
• Non-covalent bonds can be preferred if, for example, there should be the possibility that the layer of the
• polymer according to the invention is removable. This can be the case, for example, if this layer is to be replaced.
• An example of such a polymer according to the invention is a
• covalent bonds can also be preferred. These can be formed by using appropriate adhesives that bind a polymer according to the invention to the substrate. However, they can also be formed in that the substrate has compounds with radicals which, when the compound according to the invention is polymerized, with the reactive groups of the invention
• coated substrate according to the invention can be produced by applying a composition according to the invention to the uncoated substrate and then polymerizing.
• the compound according to the invention can be used as a non-stick additive in UV-NIL embossing lacquers and reduce the adhesion to work stamps (e.g. made of nickel, quartz or polymers) in the embossing process, and / or it can be used as a non-stick additive in work stamps for UV nano-stamp lithography and reduce the adhesion to the embossing lacquer in the embossing process.
• work stamps e.g. made of nickel, quartz or polymers
• the non-stick additive can permanently reduce the surface energy of UV-NIL-embossed paint surfaces and thus water and
• Dirt repellency and possibly a lotus effect on suitable micro and nano structures i.e. a self-cleaning functionality.
• the lotus effect is achieved by cleaning dirty surfaces with e.g. Alcohol reversibly regenerated.
• the compound according to the invention is suitable, inter alia, for all UV embossing lacquer formulations, for example for UV-NIL-embossed Surfaces with various structures (shark skin, moth eyes, diffraction grids).
• the compound of the present invention can be obtained by reacting an alcohol with an isocyanate.
• Branched tri- to hexa-HFPO (oligomer) alcohols bearing CF3 side groups are commercially available. Examples thereof include
• the polyols designated as CAS 14620-81-6 and CAS 141977-66-4 are preferred.
• a preferred example of such a compound according to the invention is the oligo-HFPO-urethane acrylate of the formula (I), where R can be H and n can be 3 or 4.
• PFPE-UA-3 is a compound of the formula (I) according to the invention, in which n is 3 and R is H.
• E8402 (Ebecryl 8402) is an aliphatic urethane acrylate from Allnex that is used as an embossing lacquer base.
• N-Octyl acrylate (nOA) is used as a reactive diluent.
• TPO-L is the photoinitiator ethyl (2,4,6-trimethylbenzoyl) phenylphosphinate.
• FIG. 2 shows that the contact angles of water and diiodomethane are significantly increased at very low concentrations of PFPE-UA-3 of less than 1%.
• FIG. 3 shows that the surface energy decreased significantly even at low concentrations of PFPE-UA-3, which was mainly due to the decrease in the disperse fraction of the surface energy
• the surface energies are determined using the Owens, Wendt, Rabel and Kaelble (OWRK) method (DH Kaelble, Dispersion-Polar Surface Tension Properties of Organic Solids. In: J. Adhesion 2 (1970), p. 66- 81; D. Owens; R. Wendt,
• the OWRK method is a standard method for calculating the surface free energy of a solid from the contact angle with several liquids. The surface free energy is split into a polar part and a disperse part.
• An embossing lacquer layer (75% E8402, 23% nOA, 2% TPO-L) was cured against an FPS-coated nickel sheet.
• Various concentrations of PFPE-UA-3 were used as a non-stick additive.
• FPS is 1H, 1H, 2H, 2H perfluorooctylphosphonic acid:
• SAM self-assembled monolayers
• Non-stick coating of nickel stamps is
• FIG. 5 shows that the surface energy decreased significantly even at low concentrations of PFPE-UA-3.

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• Chemical & Material Sciences (AREA)
• Organic Chemistry (AREA)
• Health & Medical Sciences (AREA)
• Materials Engineering (AREA)
• Polymers & Plastics (AREA)
• Medicinal Chemistry (AREA)
• Life Sciences & Earth Sciences (AREA)
• Engineering & Computer Science (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Wood Science & Technology (AREA)
• Physics & Mathematics (AREA)
• General Physics & Mathematics (AREA)
• Crystallography & Structural Chemistry (AREA)
• Emergency Medicine (AREA)
• Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
• Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
• Paints Or Removers (AREA)
• Macromonomer-Based Addition Polymer (AREA)

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• 2019
  • 2019-03-11 DE DE102019106081.8A patent/DE102019106081B4/de active Active
• 2020
  • 2020-02-24 KR KR1020217032142A patent/KR102647721B1/ko active IP Right Grant
  • 2020-02-24 CN CN202080029587.2A patent/CN113748144B/zh active Active
  • 2020-02-24 CA CA3132086A patent/CA3132086A1/en not_active Abandoned
  • 2020-02-24 JP JP2021553855A patent/JP7301999B2/ja active Active
  • 2020-02-24 WO PCT/EP2020/054739 patent/WO2020182452A1/de unknown
  • 2020-02-24 EP EP20706715.8A patent/EP3938411A1/de not_active Withdrawn
  • 2020-02-24 US US17/437,183 patent/US20220204441A1/en active Pending

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