WO2017040244A1 - Coated substrates and compositions for coating substrates - Google Patents

Coated substrates and compositions for coating substrates Download PDF

Info

Publication number
WO2017040244A1
WO2017040244A1 PCT/US2016/048878 US2016048878W WO2017040244A1 WO 2017040244 A1 WO2017040244 A1 WO 2017040244A1 US 2016048878 W US2016048878 W US 2016048878W WO 2017040244 A1 WO2017040244 A1 WO 2017040244A1
Authority
WO
WIPO (PCT)
Prior art keywords
polymer
scc
scc polymer
matrix
releasable
Prior art date
Application number
PCT/US2016/048878
Other languages
French (fr)
Inventor
Steven Bitler
Julian SCHAFER
Original Assignee
Landec Corporation
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 Landec Corporation filed Critical Landec Corporation
Publication of WO2017040244A1 publication Critical patent/WO2017040244A1/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING 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
    • C09D4/00Coating 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
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING 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
    • C09D133/00Coating 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
    • C09D133/04Homopolymers or copolymers of esters
    • C09D133/06Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical

Definitions

  • the coating is formed by applying to the substrate a polymeric emulsion or solution which dries to a hard protective film.
  • compositions which (i) comprise a side chain crystalline polymer (abbreviated herein to "SCC polymer”),
  • (ii) can be applied as a liquid to a substrate, for example a flooring substrate, and
  • composition after application to the substrate, can be converted into a coating which is (a) solid, (b) is not tacky in the temperature range 15-25°C, and (c) can be triggered by heat.
  • This composition is referred to herein as a "Releasable SCC Polymer Composition", whether it is (i) a liquid which is ready to be applied, or has been applied, to a substrate, or (ii) a solid coating, or (iii) a solid coating which has been triggered by heat.
  • the term "is not tacky” is used herein to mean that the solid coating exhibits a tack value less than 25 g.cm/sec of force, measured in accordance with ASTM D2979 (see for example US 5,387,450).
  • the term "can be triggered by heat” is used herein to mean that the solid coating of Releasable SCC Polymer Composition can be subjected to heating which converts the SCC polymer from a predominantly crystalline state to a partially or fully amorphous state, which enables the coating to be removed.
  • the SCC polymer becomes a viscous liquid or a flowing gel; in other cases, the SCC polymer softens but has little or no flow.
  • sidechain crystalline polymer often abbreviated to SCC polymer or SCCP, is used to denote a polymer which contains a backbone and long side chains which (i) are attached to and extend from the backbone, and (ii) at temperatures below the melting point of the SCC polymer, can crystallize together to render the polymer predominantly crystalline.
  • the Releasable SCC Polymer Composition can comprise a single SCC polymer or two or more different SCC polymers.
  • the Releasable SCC Polymer Composition includes a matrix polymer in which the SCC polymer is dispersed.
  • the Releasable SCC Polymer Composition can be (i) an "exterior coating", the term “exterior coating” being used to denote a coating which is exposed to the ambient atmosphere, or (ii) an "interior” coating, the term “interior coating” being used to denote a coating which is covered by one or more exterior coatings.
  • the exterior coating or coatings can be composed of a conventional floor finish.
  • the Releasable SCC Polymer Composition can be in direct contact with the substrate or can be separated from the substrate by one or more intermediate (“tie” or "primer") coatings.
  • the solid Releasable SCC Polymer Composition When the solid Releasable SCC Polymer Composition is triggered by heat, the SCC polymer is converted from a fully crystalline state to a partially or fully amorphous state, thus reducing the adhesion between the Releasable SCC Polymer Composition and any adjacent surface. This in turn makes it possible for at least part of the exterior coating to be removed.
  • the Releasable SCC Polymer Composition should be heated to a temperature which is greater than the onset of melting point of the SCC polymer (hereinafter abbreviated to To) and in many cases to a temperature at least as high as the peak melting temperature of the SCC polymer (hereinafter abbreviated to Tp). Particularly if the difference between the To and the Tp of the SCC polymer is large, it is preferable to heat the SCC polymer to a temperature substantially above To.
  • the conversion of the Releasable SCC Polymer Composition into discrete parts can be accomplished in any way.
  • the discrete parts can be removed in any way.
  • this invention provides a coated floor comprising
  • a Releasable SCC Polymer Composition which (i) is in the form of a solid coating which is adjacent to (but not necessarily in direct contact with) the substrate (ii) is not tacky in the temperature range 15-25°C, (iii) can be triggered by heat, and (iv) comprises a sidechain crystalline polymer (SCC polymer) which has an onset of melting temperature, T 0 , which is higher than any temperature to which the substrate will be exposed during normal use, and a peak melting temperature, Tp, which is less than any temperature which will damage the substrate, preferably a
  • the solid coating of the Releasable SCC Polymer Composition is covered by one or more coatings of a different polymeric composition which improves the wear and/or appearance characteristics of the coated floor
  • this invention provides a Releasable SCC Polymer Composition which comprises (1) an SCC polymer which has an onset of melting temperature, To, of at least 10°C, or at least 15°C, or at least 27°C. and a peak melting temperature (Tp) of at most 120°C. and (2) a matrix polymer in which the SCC polymer is dispersed.
  • Figure 1 is a cross-section through a part of a floor substrate 12 which is covered by a coating of a Releasable SCC Polymer Composition 14,
  • Figure 2 is the same as Figure 1 , except that there is a coating 18 of an acrylic floor finish over the coating 14, and
  • Figure 3 is the same as Figure 2 except that there is a tie layer 20 between the substrate and the coating 14.
  • components A, B and C can contain only components A, B and C, or can contain not only components A, B and C but also one or more other components.
  • the method can include one or more other steps which are carried out before any of the defined steps, between two of the defined steps, or after all the defined steps (except where the context excludes that possibility).
  • At least followed by a number is used herein to denote the start of a range beginning with that number (which may be a range having an upper limit or no upper limit, depending on the variable being defined). For example, “at least 1” means 1 or more than 1 , and “at least 80%” means 80% or more than 80%.
  • At most followed by a number is used herein to denote the end of a range ending with that number (which may be a range having 1 or 0 as its lower limit, or a range having no lower limit, depending upon the variable being defined). For example, “at most 4" means 4 or less than 4, and “at most 40%” means 40% or less than 40%.
  • Particle sizes given herein are median particle sizes measured by a Horiba LA-910 laser light scattering analyzer.
  • the viscosities given herein were measured at 20°C using a Brookfield LVF viscometer with spindle #3 at 60 RPM.
  • the abbreviation T 0 is used to denote the onset of melting and the abbreviation T p is used to denote the peak crystalline melting point, both measured by means of a differential scanning calorimeter (DSC) at a rate of 10°C/minute and on the first heating cycle.
  • DSC differential scanning calorimeter
  • T p is the temperature at the peak of the DSC curve
  • T 0 is the temperature at the intersection of the baseline of the DSC peak and the onset line, the onset line being defined as the tangent to the steepest part of the DSC curve below T p .
  • VCT tile (a commercial acronym for vinyl composition tile) is used herein to denote a floor tile which is composed primarily of ground limestone, vinyl resin (typically a polymer of 95% vinyl chloride and 5% vinyl acetate) and plasticizer (typically one or more phthalate esters); ASTM F1066-04 sets out certain requirements for VCT tiles such as dimensional stability and impact and heat resistance.
  • the SCC polymers used in this invention have an onset of melting temperature, To, which is higher than any temperature to which the substrate will be exposed during normal use, and a peak melting temperature (Tp) which is less than any temperature which will damage the substrate, preferably a Tp of at most 120°C.
  • the SCC polymer has one or any possible combination of one or more of the following characteristics: -
  • the SCC polymer has a To of at least 10°C, or at least 15°C, or at least 27°C, or at least 35°C, or at least 40°C,
  • the SCC polymer has a Tp of at most 80°C, preferably at most 60°C, particularly at most 50°C,
  • the SCC polymer has a Tp and a To , measured in degrees centigrade, such that the value of (T p - To) is less than T p 0 7 , preferably less than 25°C, preferably less than 20°C, particularly less than 15°C,
  • the SCC polymer has a weight average molecular weight of at most 100,000 Da, preferably at most 50,000 Da, particularly at most 20,000 Da, and in some applications less than 10,000 Da,
  • the SCC polymer comprises units derived from one or more n-alkyl acrylates or methacrylates in proportions by weight such that the average length of the n-alkyl groups is 16-20, for example 16-18, carbon atoms, the n-alkyl groups for example containing 8-22 carbon atoms, and the polymer for example containing 90 to 98%, e.g. 94 to 97%, by weight of the units derived from one or more n-alkyl acrylates.
  • the SCC polymer comprises 90-98%, e.g. 94-97%, by weight of units derived from octadecyl acrylate and hexadecyl acrylate, the ratio of octadecyl acrylate to hexadecyl acrylate units being for example 16 to 2.
  • the SCC polymer contains, for example in amount greater than 1 %, for example 1-4%, e.g. 2-4%, or 1-3%, or 1-2%, units derived from (i) a comonomer containing a carboxylic group, e.g. methacrylic acid, and/or (ii) a comonomer containing a hydroxyl group, e.g. hydroxyethyl acrylate, hydroxyethyl methacrylate hydroxypropyl acrylate or hydroxypropyl methacrylate.
  • the SCC polymer has a heat of fusion of at least 20 Joules/g
  • the SCC polymer often also contains the residue of a chain transfer agent, e.g. n-dodecyl mercaptan or butyl mercaptopropionate or methyl benzyl alcohol, which was used during the polymerization in order to control the molecular weight of the polymer.
  • a chain transfer agent e.g. n-dodecyl mercaptan or butyl mercaptopropionate or methyl benzyl alcohol
  • the monomers can be reacted together by random, stepwise or block copolymerization.
  • the SCC polymer preferably contains little or substantially no low molecular weight oligomers or unreacted monomers.
  • the polymer preferably contains less than 2000 ppm of unreacted monomers.
  • SCC polymers can be produced using monomers which are not acrylate or methacrylates, e.g. polymers derived from vinyl esters of fatty acids, copolymers of ethylene and/or -alkenes, and polymers derived from other long chain alkyl monomers, for example as described in the US patents incorporated by reference herein.
  • the SCC polymers used in this invention are produced by emulsion polymerization.
  • the polymers prepared by emulsion polymerization preferably have a particle size of 0.07 to 0.5 ⁇ , particularly 0.1 to 0.25 ⁇ , particularly 0.1-0.15 pm. However, higher particle sizes, e.g. up to 1 ⁇ , can be used if the polymer is present in a formulation containing appropriate amounts of other ingredients to ensure film formation.
  • the larger size SCC polymer particles may alternatively be created by mechanical emulsification of melted SCC polymers prepared by bulk or solution polymerization processes. When the SCC polymer is applied to the substrate as a solution in a solvent or is melt-applied, the particle size of the SCC polymer is less relevant.
  • SCC polymers are in themselves known. Publications describing SCC polymers include U.S. Patent Nos. 4,830,855, 5,120,349, 5,156,911 , 5,254,354 5,387,450, 5,412,035, 5,469,867, 5,665,822, 5,752,926, 5,783,302, 5,807,291 , 5,826,584, 6,199,318 6,255,367, 6,376,032, 6,492,462, 6,540,984, 6,544,453, 6,831 ,116, 6,989,417, 7,101 ,928, 7,169,451 , 7,175,632, 7,449,511 , 7,182,951 , 7,291 ,389 and 8,114,883; J. Poly.
  • the Releasable SCC Polymer Composition applied to the substrate preferably contains additional ingredients which make it easier to form a thin, continuous and crack-free coating containing the SCC polymer.
  • the additional ingredients may include, but are not limited to, non-crystalline polymers, water, solvents, diluents, wetting agents, thickeners, plasticizers and/or other additives that aid in the application, spreading and film formation of the coating.
  • the choice of additional ingredients preferably takes into account the physical and chemical properties of the surface of the substrate on which the Releasable SCC Polymer Composition is to be formed and the physical and chemical properties of any other coating later applied over the Releasable SCC Polymer Composition.
  • one of the additional ingredients which remains in the final coating is a matrix polymer in which the SCC polymer is dispersed.
  • the matrix polymer provides film-forming properties to the Releasable SCC Polymer
  • the matrix polymer comprises one or more polymers, each of which is at least partially amorphous, and may be substantially amorphous, and which preferably is a film-forming polymer in the absence of plasticizers or coalescing solvents.
  • the matrix polymer may contain plasticizers and/or coalescing solvents to provide or enhance the film-forming properties of the matrix polymer.
  • the matrix polymer is a styrene-acrylic polymer, or another acrylic polymer, the polymer containing 0-25%, e.g. 1-25%, or 0-20%, e.g. 1-20%, or 0-15%, e.g. 1-15%, or 0-5%, e.g. 1-5%, of units derived from one or more monomers containing carboxylic groups, for example methacrylic acid.
  • the matrix polymer is a styrene-acrylic polymer, or another acrylic polymer, the polymer being present, in the liquid Releasable SCC Polymer Composition in the form of an emulsion.
  • the styrene-acrylic polymer or other acrylic polymer can be a core shell styrene-acrylic polymer or another core shell acrylic polymer.
  • the matrix polymer can for example be (i) a polymer which is not cross- linked and which has a molecular weight of up to 100,000, or (ii) a cross-linked polymer which has a molecular weight of over 100,000 or a gel with an infinite molecular weight.
  • the matrix polymer can for example have (i) an average particle size of 0.05-0.2 pm, e.g. 0.05-0.10 pm and/or (ii) an acid monomer content of 0-20 %, or 0.5%, e.g. 1-5% and/or (iiii) a pH of 2-10, or 5-9, or 2-6..
  • the matrix polymer optionally has an MFFT below 20°C.
  • Examples of such matrix polymer include Raykote 1610 (50% NV, 7°C MFFT), Raytech 22053 (40.9 % NV, 2 °C MFFT) and Rayflex 610 (58% NV, 0°C MFFT).
  • the MFFT of a polymer can be measured by ASTM D2354.
  • the Releasable SCC Polymer Composition contains (a) 10-80%, or 30-80%, or 30-60%, e.g. 50-60%, of the SCC polymer and (b) 20-70%, for example 30-60% or 40-50%, of the matrix polymer.
  • the invention includes the possibility that the Releasable SCC Polymer
  • Composition contains 1-99% of the SCC polymer.
  • Releasable SCC Polymer Composition include (i) water and/or other ingredients, e.g.
  • the additional ingredients can include (i) thickeners, to decrease the tendency of a low solids coating to crawl and retract from the edges of the substrate due to poor wetting, for example in amount 0.1-0.2% solids on the total formulation, e.g. Acrysol TT- 935, Acrysol TT-615 and the other hydrophobically-modified alkali swellable emulsions, (ii) surface tension reducers, for example in amount 0.05-0.4% or 0.1- 0.4% solids on the total formulation, e.g.
  • the composition when it is ready to be applied to the substrate, preferably contains other ingredients including, but not limited to, one or more matrix polymers, water, one or more surfactants, and one or more cosolvents.
  • the composition can also contain additional ingredients which remain in the solid coating of the Releasable SCC Polymer Coating, and which improve the compatibility between (i) the coating and the substrate to which the liquid Releasable SCC Polymer Composition is applied and/or (ii) an exterior coating which is applied on top of the Releasable SCC Polymer Composition.
  • the Releasable SCC Polymer Composition comprises a matrix polymer having one or any possible combination of two or more of the following optional characteristics: -.
  • the matrix polymer has a minimum film forming temperature
  • the matrix polymer is an acrylic or styrene-acrylic polymer prepared by emulsion polymerization, for example a cross-linked styrene- ethylhexylacrylate-methacrylic acid polymer, a styrene-butylacrylate- methacrylic acid polymer, a styrene-butylacrylate-methylmethacrylate- methacrylic acid polymer, or an isobutyl methacrylate-methylmethacrylate- hydroxyethyl acrylate polymer,
  • the matrix polymer is composed of particles which are smaller than the particles of the SCC polymer
  • the matrix polymer forms a continuous phase in which the SCC polymer is dispersed in the form of particles.
  • the Releasable SCC Polymer Composition is in the form of a solid coating which has a thickness of less than 10 ⁇ , preferably less than 5 pm, or less than 2 ⁇ , e.g. less than 1 ⁇ .
  • the solid coating of the Releasable SCC Polymer Composition directly contacts the flooring substrate.
  • it is separated from the flooring substrate by an intermediate ("tie" or "primer") layer, for example an intermediate layer comprising a polymeric composition which is not a Releasable SCC Polymer Composition and which optionally does not include an SCC polymer.
  • the tie layer can make it easier to form a coating of the Releasable SCC Polymer Composition on the substrate and/or to subsequently remove part or all of a solid coating of the Releasable SCC Polymer Coating.
  • the surface of the substrate has a porous, matte or otherwise non-uniform and non-glossy surface
  • a tie layer which is between the substrate and the solid coating of the Releasable SCC Polymer Composition. This can makes it easier to form a uniform coating of the
  • the Releasable SCC Polymer Composition and/or can reduce the number of outer coats which need to be applied over the solid coating of the Releasable SCC Polymer Composition in order to achieve a satisfactory appearance.
  • the tie layer has sufficient abrasion resistance to ensure that it remains in place after the Releasable SCC Polymer Composition has been removed.
  • Polyurethane compositions have been found to be particularly useful as tie base coats.
  • Exemplary tie layers include traditional floor finishes, including crosslinked and non-crosslinked coatings such as acrylic polymer (including uv-cured acrylic polymer), polyurethane (including uv-cured polyurethane and polyurethane that is not uv-cured), polyurea, epoxy polymer (including uv-cured epoxy polymer), polysiloxane, vinyl polymer, styrene-butadiene polymer, as well as factory- applied coatings, concrete treatments, penetrating sealers, densifiers and other suitable coatings and treatments known to those skilled in the art.
  • a tie layer may have a dry weight coating thickness of about 0.01 mil to about 100 mil.
  • an exterior coating on top of the solid coating of the Releasable SCC Polymer Composition for example an exterior coating which comprises one or more coatings of a commercially available flooring finish.
  • the wear coating can for example be a coating formed from a coating composition as disclosed in US 5,977,228 (Mauer), International Publication WO 1999/000459 or International Publication W02012/162641. The entire content of each of those publications is incorporated herein by reference for all purposes.
  • the coatings may have the same or different compositions.
  • the substrate which carries the Releasable SCC Polymer Composition can be of any kind, but the invention is particularly useful when the substrate is a fixed floor surface or a substrate, for example a VCT tile or linoleum, which can be secured to a fixed substrate to provide a fixed floor surface.
  • the substrate is a vinyl composition tile (VCT).
  • VCT vinyl composition tile
  • Such tiles are well known and are composed primarily of ground limestone, vinyl resin (typically a polymer of 95% vinyl chloride and 5% vinyl acetate) and plasticizer (typically one or more phthalate esters); ASTM F1066-04 sets out certain requirements for VCTs such as dimensional stability and impact and heat resistance.
  • VCTs are frequently supplied with an upper surface coating of a thin (about 0.2 mil thick) acrylic lacquer sealer. Often, after the tiles have been secured to the rigid substrate, they are given three or four coatings of a conventional acrylic VCT finish, in order to produce a desirable glossy and wear- resistant surface.
  • the Releasable SCC Polymer Composition can be formed directly on a VCT, whether or not the VCT has a surface coating of an acrylic lacquer sealer. After the Releasable SCC Polymer Composition has been formed, one or more coats, e.g. 3-6 coats, of a conventional floor finish can optionally be applied so that the finished floor has desired durability and appearance.
  • This example shows the preparation of SCC polymers suitable for use in this invention.
  • Table 1 sets out the monomers which were used to prepare Polymers 390-18, 390-28, 390-38, 390-44, 390-58, 390-78 and 390-100.
  • Table 2 sets out the properties of the prepared polymers.
  • the polymers shown in Table 1 were prepared by delayed feed free-radical initiated redox polymerization of monomer emulsions to produce variations in molecular weight, acid functionality and melt transition temperature. The monomers were melted and blended at 45-50°C with a mercaptan chain transfer agent. The resulting mixture
  • This example shows the conversion of SCC polymers 390-38 and 390-44 into SCC polymer compositions suitable for coating on a substrate, using a 10 stepwise blending procedure to incorporate the less compatible ingredients with the polymer emulsions.
  • a polymer mixture was prepared from the ingredients shown in Table 3 below.
  • the resulting polymer mixture was blended with the diluent mixture shown in Table 4, to produce an SCC polymer composition having the physical properties show in Table 4.

Abstract

A coated floor comprising (1) a flooring substrate, and (2) a solid SCC polymer coating which is adjacent to the substrate and which comprises a sidechain crystalline polymer (SCC polymer) which has now an onset of melting temperature, T0, of at least 27°C and a peak melting temperature (Tp) of at most 120°C. The SCC polymer coating can be an exterior coating or can be covered by one or more exterior coatings, for example of a commercial flooring finish.

Description

TITLE.
Coated Substrates and Compositions for Coating Substrates.
INVENTORS. Julian Schafer and Steven Bitler
CROSS-REFERENCE TO RELATED APPLICATIONS.
This application claims priority from, and the benefit of, US Provisional Application No. 62/211,274 filed August 28, 2015. The entire content of that provisional application is incorporated herein by reference for all purposes. This application is also related to (1) each of the other PCT applications filed on the same day as this application and claiming priority from US Provisional
Application No. 62/211,274 filed August 28, 2015, (2) US Provisional Application No. 62/211 ,350, filed August 28, 2015, and entitled Apparatus for Treating Coated Substrates, (3) the PCT application filed on the same day as this application and claiming priority from US Provisional Application No. 62/211 ,350, (4) US Provisional Application No. 62/211,324 filed August 28, 2015, and entitled Temperature-Releasable Floor Coating System, and (5) the PCT application filed on the same day as this application and claiming priority from US Provisional Application No. 62/611 ,324 filed August 28, 2015. The entire content of each of those related applications is incorporated herein by reference for all purposes. BACKGROUND OF THE INVENTION.
It is well known to protect and enhance the appearance of substrates, e.g. floors and countertops, by the application of a surface coating. In many cases, the coating is formed by applying to the substrate a polymeric emulsion or solution which dries to a hard protective film.
The surface coating on the floors of commercial establishments needs to be replaced at regular intervals. Many commercial floor finishes are based on acrylate polymers which are cross-linked using metal ions. The replacement of such floor coatings requires the use of alkaline strippers with consequences which are well known to be highly undesirable. Other floor coatings have better wear resistance than acrylate polymers, but must be removed mechanically, e.g. by sanding, which creates dust and which can damage the flooring substrate.
Other surface coatings which may need to be removed are (i) coatings which were originally useful but which now need to be replaced and/or removed, e.g. labels, decals, wallpaper or paint, and (ii) coatings which were never desired, e.g. graffiti.
SUMMARY OF THE INVENTION.
This invention is concerned with coatings which can be removed without using alkaline strippers. The invention makes use of compositions which (i) comprise a side chain crystalline polymer (abbreviated herein to "SCC polymer"),
(ii) can be applied as a liquid to a substrate, for example a flooring substrate, and
(iii) after application to the substrate, can be converted into a coating which is (a) solid, (b) is not tacky in the temperature range 15-25°C, and (c) can be triggered by heat. This composition is referred to herein as a "Releasable SCC Polymer Composition", whether it is (i) a liquid which is ready to be applied, or has been applied, to a substrate, or (ii) a solid coating, or (iii) a solid coating which has been triggered by heat.
The term "is not tacky" is used herein to mean that the solid coating exhibits a tack value less than 25 g.cm/sec of force, measured in accordance with ASTM D2979 (see for example US 5,387,450).
The term "can be triggered by heat" is used herein to mean that the solid coating of Releasable SCC Polymer Composition can be subjected to heating which converts the SCC polymer from a predominantly crystalline state to a partially or fully amorphous state, which enables the coating to be removed. In some cases, when the Releasable SCC Polymer Composition is triggered by heat, the SCC polymer becomes a viscous liquid or a flowing gel; in other cases, the SCC polymer softens but has little or no flow.
The term "sidechain crystalline polymer", often abbreviated to SCC polymer or SCCP, is used to denote a polymer which contains a backbone and long side chains which (i) are attached to and extend from the backbone, and (ii) at temperatures below the melting point of the SCC polymer, can crystallize together to render the polymer predominantly crystalline.
The Releasable SCC Polymer Composition can comprise a single SCC polymer or two or more different SCC polymers. In many cases, the Releasable SCC Polymer Composition includes a matrix polymer in which the SCC polymer is dispersed.
The Releasable SCC Polymer Composition can be (i) an "exterior coating", the term "exterior coating" being used to denote a coating which is exposed to the ambient atmosphere, or (ii) an "interior" coating, the term "interior coating" being used to denote a coating which is covered by one or more exterior coatings. The exterior coating or coatings can be composed of a conventional floor finish. The Releasable SCC Polymer Composition can be in direct contact with the substrate or can be separated from the substrate by one or more intermediate ("tie" or "primer") coatings.
When the solid Releasable SCC Polymer Composition is triggered by heat, the SCC polymer is converted from a fully crystalline state to a partially or fully amorphous state, thus reducing the adhesion between the Releasable SCC Polymer Composition and any adjacent surface. This in turn makes it possible for at least part of the exterior coating to be removed.
It is preferred that the Releasable SCC Polymer Composition should be heated to a temperature which is greater than the onset of melting point of the SCC polymer (hereinafter abbreviated to To) and in many cases to a temperature at least as high as the peak melting temperature of the SCC polymer (hereinafter abbreviated to Tp). Particularly if the difference between the To and the Tp of the SCC polymer is large, it is preferable to heat the SCC polymer to a temperature substantially above To.
The conversion of the Releasable SCC Polymer Composition into discrete parts can be accomplished in any way. The discrete parts can be removed in any way.
Particular aspects of the present invention are summarized below.
First Aspect of the Invention.
In a first aspect this invention provides a coated floor comprising
(1) a flooring substrate, and
(2) a Releasable SCC Polymer Composition which (i) is in the form of a solid coating which is adjacent to (but not necessarily in direct contact with) the substrate (ii) is not tacky in the temperature range 15-25°C, (iii) can be triggered by heat, and (iv) comprises a sidechain crystalline polymer (SCC polymer) which has an onset of melting temperature, T0, which is higher than any temperature to which the substrate will be exposed during normal use, and a peak melting temperature, Tp, which is less than any temperature which will damage the substrate, preferably a
Tp of at most 120°C.
In many cases, the solid coating of the Releasable SCC Polymer Composition is covered by one or more coatings of a different polymeric composition which improves the wear and/or appearance characteristics of the coated floor
Second Aspect of the Invention
In a second aspect, this invention provides a Releasable SCC Polymer Composition which comprises (1) an SCC polymer which has an onset of melting temperature, To, of at least 10°C, or at least 15°C, or at least 27°C. and a peak melting temperature (Tp) of at most 120°C. and (2) a matrix polymer in which the SCC polymer is dispersed.
BRIEF DESCRIPTION OF THE DRAWINGS.
The invention is illustrated in the accompanying illustrative drawings which are diagrammatic and not to scale and in which
Figure 1 is a cross-section through a part of a floor substrate 12 which is covered by a coating of a Releasable SCC Polymer Composition 14,
Figure 2 is the same as Figure 1 , except that there is a coating 18 of an acrylic floor finish over the coating 14, and
Figure 3 is the same as Figure 2 except that there is a tie layer 20 between the substrate and the coating 14.
DETAILED DESCRIPTION OF THE INVENTION.
In the Summary of the Invention above and in the Detailed Description of the Invention, the Examples, and the Claims below, and in the attached drawings, reference is made to particular features (including method steps) of the invention. It is to be understood that the disclosure of the invention in this specification includes all appropriate combinations of such particular features. For example, where a particular feature is disclosed in the context of a particular aspect or embodiment of the invention, or a particular claim, that feature can also be used, to the extent appropriate, in combination with and/or in the context of other particular aspects and embodiments of the invention, and in the invention generally.
The term "comprises" and grammatical equivalents thereof are used herein to mean that other elements (i.e. components, ingredients, steps etc.) are optionally present. For example, a structure "comprising" (or "which comprises") components A, B and C can contain only components A, B and C, or can contain not only components A, B and C but also one or more other components.
The term "consisting essentially of and grammatical equivalents thereof is used herein to mean that other elements may be present which do not materially alter the disclosed invention.
Where reference is made herein to a method comprising two or more defined steps, the defined steps can be carried out in any order or
simultaneously (except where the context excludes that possibility), and the method can include one or more other steps which are carried out before any of the defined steps, between two of the defined steps, or after all the defined steps (except where the context excludes that possibility).
The term "at least" followed by a number is used herein to denote the start of a range beginning with that number (which may be a range having an upper limit or no upper limit, depending on the variable being defined). For example, "at least 1" means 1 or more than 1 , and "at least 80%" means 80% or more than 80%.
The term "at most" followed by a number is used herein to denote the end of a range ending with that number (which may be a range having 1 or 0 as its lower limit, or a range having no lower limit, depending upon the variable being defined). For example, "at most 4" means 4 or less than 4, and "at most 40%" means 40% or less than 40%.
When, in this specification, a range is given as "(a first number) to (a second number)" or "(a first number) - (a second number)", this means a range whose lower limit is the first number and whose upper limit is the second number.
For example, "from 2 to 16" or "2-16" means a range whose lower limit is 2 and whose upper limit is 16. The numbers given herein should be construed with the latitude appropriate to their context and expression.
The terms "a", "an" and "the" before an item are used herein to mean that there can be a single such item or two or more such items, unless the context makes this impossible.
The term "plurality" is used herein to mean two or more.
In describing and claiming the invention below, the following
abbreviations, definitions, and methods of measurement (in addition to those already given) are used.
Parts and percentages are by weight, unless otherwise noted.
Temperatures are in degrees centigrade, unless otherwise noted.
Particle sizes given herein are median particle sizes measured by a Horiba LA-910 laser light scattering analyzer.
The viscosities given herein were measured at 20°C using a Brookfield LVF viscometer with spindle #3 at 60 RPM. The abbreviation T0 is used to denote the onset of melting and the abbreviation Tp is used to denote the peak crystalline melting point, both measured by means of a differential scanning calorimeter (DSC) at a rate of 10°C/minute and on the first heating cycle.
To and Tp are measured in the conventional way well known to those skilled in the art. Thus Tp is the temperature at the peak of the DSC curve, and T0 is the temperature at the intersection of the baseline of the DSC peak and the onset line, the onset line being defined as the tangent to the steepest part of the DSC curve below Tp.
The molecular weights given herein were measured by gel permeation chromatography using a Perkin-Elmer Series 200 Autosampler and Binary LC pump with 3 Phenomenex GPC columns in two Series 200Peltier Column Ovens followed by a Series 200a refractive index detector and ASTRA software.
The term "VCT tile" (a commercial acronym for vinyl composition tile) is used herein to denote a floor tile which is composed primarily of ground limestone, vinyl resin (typically a polymer of 95% vinyl chloride and 5% vinyl acetate) and plasticizer (typically one or more phthalate esters); ASTM F1066-04 sets out certain requirements for VCT tiles such as dimensional stability and impact and heat resistance.
The SCC Polymers Used in This Invention.
The SCC polymers used in this invention have an onset of melting temperature, To, which is higher than any temperature to which the substrate will be exposed during normal use, and a peak melting temperature (Tp) which is less than any temperature which will damage the substrate, preferably a Tp of at most 120°C.
In various embodiments of the invention, the SCC polymer has one or any possible combination of one or more of the following characteristics: -
(a) the SCC polymer has a To of at least 10°C, or at least 15°C, or at least 27°C, or at least 35°C, or at least 40°C,
(b) the SCC polymer has a Tp of at most 80°C, preferably at most 60°C, particularly at most 50°C,
(c) the SCC polymer has a Tp and a To , measured in degrees centigrade, such that the value of (Tp - To) is less than Tp 0 7 , preferably less than 25°C, preferably less than 20°C, particularly less than 15°C,
(d) the SCC polymer has a weight average molecular weight of at most 100,000 Da, preferably at most 50,000 Da, particularly at most 20,000 Da, and in some applications less than 10,000 Da,
(e) the SCC polymer has been prepared by an emulsion
polymerization process which produces particles having a size of 0.07 to 0.5 μητι, particularly 0.1 to 0.25 μητι,
(f) the SCC polymer comprises units derived from one or more n-alkyl acrylates or methacrylates in proportions by weight such that the average length of the n-alkyl groups is 16-20, for example 16-18, carbon atoms, the n-alkyl groups for example containing 8-22 carbon atoms, and the polymer for example containing 90 to 98%, e.g. 94 to 97%, by weight of the units derived from one or more n-alkyl acrylates.
(g) the SCC polymer comprises 90-98%, e.g. 94-97%, by weight of units derived from octadecyl acrylate and hexadecyl acrylate, the ratio of octadecyl acrylate to hexadecyl acrylate units being for example 16 to 2. (h) the SCC polymer contains, for example in amount greater than 1 %, for example 1-4%, e.g. 2-4%, or 1-3%, or 1-2%, units derived from (i) a comonomer containing a carboxylic group, e.g. methacrylic acid, and/or (ii) a comonomer containing a hydroxyl group, e.g. hydroxyethyl acrylate, hydroxyethyl methacrylate hydroxypropyl acrylate or hydroxypropyl methacrylate.
(i) the SCC polymer has a heat of fusion of at least 20 Joules/g The SCC polymer often also contains the residue of a chain transfer agent, e.g. n-dodecyl mercaptan or butyl mercaptopropionate or methyl benzyl alcohol, which was used during the polymerization in order to control the molecular weight of the polymer.
The monomers can be reacted together by random, stepwise or block copolymerization.
The SCC polymer preferably contains little or substantially no low molecular weight oligomers or unreacted monomers. For example, the polymer preferably contains less than 2000 ppm of unreacted monomers.
Other SCC polymers can be produced using monomers which are not acrylate or methacrylates, e.g. polymers derived from vinyl esters of fatty acids, copolymers of ethylene and/or -alkenes, and polymers derived from other long chain alkyl monomers, for example as described in the US patents incorporated by reference herein.
In some embodiments the SCC polymers used in this invention are produced by emulsion polymerization. The polymers prepared by emulsion polymerization preferably have a particle size of 0.07 to 0.5 μ, particularly 0.1 to 0.25 μ, particularly 0.1-0.15 pm. However, higher particle sizes, e.g. up to 1 μ, can be used if the polymer is present in a formulation containing appropriate amounts of other ingredients to ensure film formation. The larger size SCC polymer particles may alternatively be created by mechanical emulsification of melted SCC polymers prepared by bulk or solution polymerization processes. When the SCC polymer is applied to the substrate as a solution in a solvent or is melt-applied, the particle size of the SCC polymer is less relevant. SCC polymers are in themselves known. Publications describing SCC polymers include U.S. Patent Nos. 4,830,855, 5,120,349, 5,156,911 , 5,254,354 5,387,450, 5,412,035, 5,469,867, 5,665,822, 5,752,926, 5,783,302, 5,807,291 , 5,826,584, 6,199,318 6,255,367, 6,376,032, 6,492,462, 6,540,984, 6,544,453, 6,831 ,116, 6,989,417, 7,101 ,928, 7,169,451 , 7,175,632, 7,449,511 , 7,182,951 , 7,291 ,389 and 8,114,883; J. Poly. Sci. 60, 19 (1962), J. Poly. Sci, (Polymer Chemistry) 7, 3053 (1969), 9, 1835, 3349, 3351 , 3367, 10, 1657, 3347, 18, 2197, 19, 871 , J. Poly. Sci, Poly-Physics Ed 18 2197 (1980), J. Poly. Sci, Macromol. Rev, 8, 117 (1974), Macromolecules 12, 94 (1979), 13, 12, 15, 18, 2141 , 19, 611 , JACS 75, 3326 (1953), 76; 6280, Polymer J 17, 991 (1985); and Poly. Sci USSR 21 , 241 (1979). The entire disclosure of each of those United States Patents and publications is incorporated in this specification by reference.
Preparation of the SCC Polymers.
Those skilled in the art of the SCC polymers are conversant with the known methods for preparing SCC polymers. Reference may be made, for example, to the patents and publications incorporated by reference, for example US 6,540,984 and US 7,175,832 describing emulsion polymerization methods. Those skilled in the art, having regard to their own knowledge and the disclosure in this specification, will have no difficulty in preparing SCC polymers which are useful in this invention.
Releasable SCC Polymer Compositions Containing Additional Ingredients.
When the SCC polymer has been produced by emulsion polymerization, it is difficult to make the SCC polymer particles coalesce, when the SCC polymer is dried at temperatures less than To, to form a continuous and crack-free coating. To avoid or limit the need to dry the SCC polymer emulsion at an elevated temperature, the Releasable SCC Polymer Composition applied to the substrate preferably contains additional ingredients which make it easier to form a thin, continuous and crack-free coating containing the SCC polymer. The additional ingredients may include, but are not limited to, non-crystalline polymers, water, solvents, diluents, wetting agents, thickeners, plasticizers and/or other additives that aid in the application, spreading and film formation of the coating. The choice of additional ingredients preferably takes into account the physical and chemical properties of the surface of the substrate on which the Releasable SCC Polymer Composition is to be formed and the physical and chemical properties of any other coating later applied over the Releasable SCC Polymer Composition.
Preferably one of the additional ingredients which remains in the final coating is a matrix polymer in which the SCC polymer is dispersed. The matrix polymer provides film-forming properties to the Releasable SCC Polymer
Composition. The matrix polymer comprises one or more polymers, each of which is at least partially amorphous, and may be substantially amorphous, and which preferably is a film-forming polymer in the absence of plasticizers or coalescing solvents. However, the matrix polymer may contain plasticizers and/or coalescing solvents to provide or enhance the film-forming properties of the matrix polymer.
In some embodiments, the matrix polymer is a styrene-acrylic polymer, or another acrylic polymer, the polymer containing 0-25%, e.g. 1-25%, or 0-20%, e.g. 1-20%, or 0-15%, e.g. 1-15%, or 0-5%, e.g. 1-5%, of units derived from one or more monomers containing carboxylic groups, for example methacrylic acid.
In some embodiments, the matrix polymer is a styrene-acrylic polymer, or another acrylic polymer, the polymer being present, in the liquid Releasable SCC Polymer Composition in the form of an emulsion. The styrene-acrylic polymer or other acrylic polymer can be a core shell styrene-acrylic polymer or another core shell acrylic polymer.
The matrix polymer can for example be (i) a polymer which is not cross- linked and which has a molecular weight of up to 100,000, or (ii) a cross-linked polymer which has a molecular weight of over 100,000 or a gel with an infinite molecular weight.
The matrix polymer can for example have (i) an average particle size of 0.05-0.2 pm, e.g. 0.05-0.10 pm and/or (ii) an acid monomer content of 0-20 %, or 0.5%, e.g. 1-5% and/or (iiii) a pH of 2-10, or 5-9, or 2-6..
The matrix polymer optionally has an MFFT below 20°C. Examples of such matrix polymer include Raykote 1610 (50% NV, 7°C MFFT), Raytech 22053 (40.9 % NV, 2 °C MFFT) and Rayflex 610 (58% NV, 0°C MFFT). The MFFT of a polymer can be measured by ASTM D2354.
In some embodiments, the Releasable SCC Polymer Composition contains (a) 10-80%, or 30-80%, or 30-60%, e.g. 50-60%, of the SCC polymer and (b) 20-70%, for example 30-60% or 40-50%, of the matrix polymer. However, the invention includes the possibility that the Releasable SCC Polymer
Composition contains 1-99% of the SCC polymer.
Other additional ingredients which are optionally present in the Releasable SCC Polymer Composition include (i) water and/or other ingredients, e.g.
solvents, which evaporate after the composition has been applied to, and dried on, the substrate, and which are not, therefore, present in the final coating, and (ii) one or more other ingredients which remain in the final coating. The additional ingredients can include (i) thickeners, to decrease the tendency of a low solids coating to crawl and retract from the edges of the substrate due to poor wetting, for example in amount 0.1-0.2% solids on the total formulation, e.g. Acrysol TT- 935, Acrysol TT-615 and the other hydrophobically-modified alkali swellable emulsions, (ii) surface tension reducers, for example in amount 0.05-0.4% or 0.1- 0.4% solids on the total formulation, e.g. Fluorad FC-4432, Fluorad FC-129, Capstone FS-60 and Zonyl FSO, (iii) wetting and anti-foaming agents, for example in amount 0.05-0.25% solids on the total formulation, e.g. Surfynol
104A, Surfynol 104PA and Surfynol 485W, (iv) water-soluble solvents to improve film spreading, substrate wetting and interfacial adhesion, for example in amount 1-5% of the composition as it is applied to the substrate, e.g. glycol ethers and alcohols, and (v) plasticizers or coalescent agents to improved film formation during drying at ambient temperature.
Thus, the composition, when it is ready to be applied to the substrate, preferably contains other ingredients including, but not limited to, one or more matrix polymers, water, one or more surfactants, and one or more cosolvents. The composition can also contain additional ingredients which remain in the solid coating of the Releasable SCC Polymer Coating, and which improve the compatibility between (i) the coating and the substrate to which the liquid Releasable SCC Polymer Composition is applied and/or (ii) an exterior coating which is applied on top of the Releasable SCC Polymer Composition.
In particular embodiments of the invention, the Releasable SCC Polymer Composition comprises a matrix polymer having one or any possible combination of two or more of the following optional characteristics: -.
(a) the matrix polymer has a minimum film forming temperature
(MFFT) which is at most 20°C,
(b) the matrix polymer has a minimum film forming temperature
(MFFT) which is at least 20°C
(c) the matrix polymer is miscible with water,
(d) the matrix polymer is an acrylic or styrene-acrylic polymer prepared by emulsion polymerization, for example a cross-linked styrene- ethylhexylacrylate-methacrylic acid polymer, a styrene-butylacrylate- methacrylic acid polymer, a styrene-butylacrylate-methylmethacrylate- methacrylic acid polymer, or an isobutyl methacrylate-methylmethacrylate- hydroxyethyl acrylate polymer,
(e) the matrix polymer is composed of particles which are smaller than the particles of the SCC polymer, and
(f) the matrix polymer forms a continuous phase in which the SCC polymer is dispersed in the form of particles.
Additional Details of the Releasable SCC Polymer Composition and Other Coatings.
In some embodiments of the invention, the Releasable SCC Polymer Composition is in the form of a solid coating which has a thickness of less than 10 μιη, preferably less than 5 pm, or less than 2 μιη, e.g. less than 1 μιη. There can be two or more solid coatings each of which is a Releasable SCC Polymer Composition. When there are two or more such coatings, they are preferably applied separately and optionally can be separated by one or more polymeric coatings which are not composed of a Releasable SCC Polymer Composition, for example a polymeric coating which is not a Releasable SCC Polymer
Composition , for example does not contain an SCC polymer, or a polymeric composition suitable for use as a wear coating as described below. In some embodiments of the invention, the solid coating of the Releasable SCC Polymer Composition directly contacts the flooring substrate. In other embodiments, it is separated from the flooring substrate by an intermediate ("tie" or "primer") layer, for example an intermediate layer comprising a polymeric composition which is not a Releasable SCC Polymer Composition and which optionally does not include an SCC polymer. The tie layer can make it easier to form a coating of the Releasable SCC Polymer Composition on the substrate and/or to subsequently remove part or all of a solid coating of the Releasable SCC Polymer Coating.
Particularly if the surface of the substrate has a porous, matte or otherwise non-uniform and non-glossy surface, there is preferably a tie layer which is between the substrate and the solid coating of the Releasable SCC Polymer Composition. This can makes it easier to form a uniform coating of the
Releasable SCC Polymer Composition, and/or can reduce the number of outer coats which need to be applied over the solid coating of the Releasable SCC Polymer Composition in order to achieve a satisfactory appearance. Preferably the tie layer has sufficient abrasion resistance to ensure that it remains in place after the Releasable SCC Polymer Composition has been removed.
Polyurethane compositions have been found to be particularly useful as tie base coats.
Exemplary tie layers include traditional floor finishes, including crosslinked and non-crosslinked coatings such as acrylic polymer (including uv-cured acrylic polymer), polyurethane (including uv-cured polyurethane and polyurethane that is not uv-cured), polyurea, epoxy polymer (including uv-cured epoxy polymer), polysiloxane, vinyl polymer, styrene-butadiene polymer, as well as factory- applied coatings, concrete treatments, penetrating sealers, densifiers and other suitable coatings and treatments known to those skilled in the art. A tie layer may have a dry weight coating thickness of about 0.01 mil to about 100 mil.
In many embodiments of the invention, there is an exterior coating on top of the solid coating of the Releasable SCC Polymer Composition, for example an exterior coating which comprises one or more coatings of a commercially available flooring finish. The wear coating can for example be a coating formed from a coating composition as disclosed in US 5,977,228 (Mauer), International Publication WO 1999/000459 or International Publication W02012/162641. The entire content of each of those publications is incorporated herein by reference for all purposes.
When there is more than one coating on the substrate, the coatings may have the same or different compositions.
The Substrates Used in This Invention.
The substrate which carries the Releasable SCC Polymer Composition can be of any kind, but the invention is particularly useful when the substrate is a fixed floor surface or a substrate, for example a VCT tile or linoleum, which can be secured to a fixed substrate to provide a fixed floor surface.
In one embodiment of the invention, the substrate is a vinyl composition tile (VCT). Such tiles are well known and are composed primarily of ground limestone, vinyl resin (typically a polymer of 95% vinyl chloride and 5% vinyl acetate) and plasticizer (typically one or more phthalate esters); ASTM F1066-04 sets out certain requirements for VCTs such as dimensional stability and impact and heat resistance.
VCTs are frequently supplied with an upper surface coating of a thin (about 0.2 mil thick) acrylic lacquer sealer. Often, after the tiles have been secured to the rigid substrate, they are given three or four coatings of a conventional acrylic VCT finish, in order to produce a desirable glossy and wear- resistant surface.
The Releasable SCC Polymer Composition can be formed directly on a VCT, whether or not the VCT has a surface coating of an acrylic lacquer sealer. After the Releasable SCC Polymer Composition has been formed, one or more coats, e.g. 3-6 coats, of a conventional floor finish can optionally be applied so that the finished floor has desired durability and appearance.
Examples.
The invention is illustrated by the following Examples.
Example 1.
This example shows the preparation of SCC polymers suitable for use in this invention. Table 1 below sets out the monomers which were used to prepare Polymers 390-18, 390-28, 390-38, 390-44, 390-58, 390-78 and 390-100. Table 2 below sets out the properties of the prepared polymers.
5 Table 1.
Figure imgf000016_0001
The polymers shown in Table 1 were prepared by delayed feed free-radical initiated redox polymerization of monomer emulsions to produce variations in molecular weight, acid functionality and melt transition temperature. The monomers were melted and blended at 45-50°C with a mercaptan chain transfer agent. The resulting mixture
was then emulsified into an aqueous surfactant mixture B containing:
285.2 g deionized water
15 63.0 g n-propanol
12.0 g ethoxylated C10-C12 alcohol sulfosuccinate disodium salt, 31%
5.7 g ethoxylated C16-C18 alcohol
4.1 g ethoxylated C12-C14 secondary alcohol
0.2 g t-butyl hydroperoxide, 70% in water The resulting monomer emulsion, kept warm at 38-42°C in a jacketed glass feeding tank, was pumped to a stirred reactor at 63-65°C containing:
320.1 g deionized water
0.03 g hydroxyethyl EDTA, ferric complex
63.1 g n-propanol
13.5 g ethoxylated C10-C12 alcohol sulfosuccinate disodium salt, 31% 4.5 g sodium alpha C12-14 olefin sulfonate, 35%
0.6 g ethoxylated C12-C14 secondary alcohol
30.0 g styrene-acrylic seed polymer, 0.05-0.06 micron particle size J simultaneously with a delayed feed of activator solution:
0.45 g hydroxy methane sulfinic acid, sodium salt
24.7 g deionized water
4.8 g n-propanol while maintaining reactor contents at 63-65°C for two hours until all feeds were completed.
The following initiator and activator solutions were pumped into the reactor over 80 minutes at 62-63°C in order to reduce un-reacted monomer levels:
Initiator:
0.38 g t-butyl hydroperoxide
1.08 g ethoxylated C12-C14 secondary alcohol
1.25 g water
Activator:
0.60 g hydroxymethane sulfinic acid, sodium salt
19.5 g water After feeds were completed and contents cooled to 38°C, pH was adjusted to 7.3 with 25% aqueous ammonia. After cooling to room temperature, the product was filtered through 200 mesh screen yielding about 1.3 kg of emulsion.
5 Table 2
Figure imgf000018_0001
Example 2.
This example shows the conversion of SCC polymers 390-38 and 390-44 into SCC polymer compositions suitable for coating on a substrate, using a 10 stepwise blending procedure to incorporate the less compatible ingredients with the polymer emulsions. In the first step, a polymer mixture was prepared from the ingredients shown in Table 3 below. In the second step, the resulting polymer mixture was blended with the diluent mixture shown in Table 4, to produce an SCC polymer composition having the physical properties show in Table 4.
Table 3.
Figure imgf000019_0001
Table 4.
Figure imgf000020_0001

Claims

CLAIMS.
1. A coated floor comprising
(1) a flooring substrate, and
(2) a solid coating of a Releasable SCC Polymer Composition which (i) is adjacent to the substrate, (ii) can be triggered by heat and (iii) comprises a sidechain crystalline polymer (SCC polymer) which has an onset of melting temperature, T0, which is higher than any temperature to which the substrate will be exposed during normal use and a peak melting temperature (Tp) which is less than any temperature which will damage the substrate, preferably a Tp of at most 120°C.
2. A coated floor according to claim 1 wherein the SCC polymer has one or more of the following characteristics
(a) the SCC polymer has a To of at least 10°C, or at least 15°C, or at least 27°C, or at least 35°C, or at least 40°C,
(b) the SCC polymer has a Tp of at most 80°C, preferably at most 60°C, particularly at most 50°C,
(c) the SCC polymer has a Tp and a To , measured in degrees centigrade, such that the value of (Tp - T0) is less than Tp 0 7, preferably less than 25°C, preferably less than 20°C, particularly less than 15°C,
(d) the SCC polymer has a weight average molecular weight of at most 100,000 Da, preferably at most 50,000 Da, particularly at most 20,000 Da, and in some applications less than 10,000 Da,
(e) the SCC polymer has been prepared by an emulsion
polymerization process which produces particles having a size of 0.07 to 0.5 pm, particularly 0.1 to 0.25 pm,
(f) the SCC polymer comprises units derived from one or more n-alkyl acrylates or methacrylates in proportions by weight such that the average length of the n-alkyl groups is 6-20, for example 16-18, carbon atoms, the n-alkyl groups for example containing 8-22 carbon atoms, and the polymer for example containing 90 to 98%, e.g. 94 to 97%, by weight of the units derived from one or more n-alkyl acrylates. (g) the SCC polymer comprises 90-98%, e.g. 94-97%, by weight of units derived from octadecyl acrylate and hexadecyl acrylate, the ratio of octadecyl acrylate to hexadecyl acrylate units being for example 16 to 2.
(h) the SCC polymer contains, for example in amount greater than 1 %, for example 1-4%, e.g. 2-4%, or 1-3%, or 1-2%, units derived from (i) a comonomer containing a carboxylic group, e.g. methacrylic acid, and/or (ii) a comonomer containing a hydroxyl group, e.g. hydroxyethyl acrylate, hydroxyethyl methacrylate hydroxypropyl acrylate or hydroxypropyl methacrylate.
(i) the SCC polymer has a heat of fusion of at least 20 Joules/g
3. A coated floor according to claim 1 or 2 wherein the Releasable SCC Polymer Composition comprises a matrix polymer.
4. A coated floor according to claim 3 wherein the matrix polymer has one or more of the following characteristics: -
(a) the matrix polymer has a minimum film forming temperature
(MFFT) which is at most 20°C,
(b) the matrix polymer has a minimum film forming temperature
(MFFT) which is at least 20°C
(c) the matrix polymer is miscible with water,
(d) the matrix polymer is an acrylic or styrene-acrylic polymer prepared by emulsion polymerization, for example a cross-linked styrene- ethylhexylacrylate-methacrylic acid polymer, a styrene-butylacrylate- methacrylic acid polymer, a styrene-butylacrylate-methylmethacrylate- methacrylic acid polymer, or an isobutyl methacrylate-methylmethacrylate- hydroxyethyl acrylate,
(e) the matrix polymer is composed of particles which are smaller than the particles of the SCC polymer, and
(f) the matrix polymer forms a continuous phase in which the SCC polymer is dispersed in the form of particles.
5. A coated floor according to claim 3 or 4 wherein the Releasable SCC Polymer Composition comprises 30-80%, e.g. 40-70% or 50-60%, of the SCC polymer and 20-70%, for example 30-60% or 40-50%, of the matrix polymer.
6. A coated floor according to any of the preceding claims wherein the Releasable SCC Polymer Composition has a thickness of less than 5 pm, preferably less than 2 pm, e.g. less than 1 pm.
7. A coated floor according to any of the preceding claims wherein the Releasable SCC Polymer Composition directly contacts the flooring substrate, or is separated from the flooring substrate by an intermediate coating comprising a polymeric composition which does not include an SCC polymer.
8. A coated floor according to any of the preceding claims wherein the flooring substrate is a vinyl composition tile.
9. A coated floor according to any of the preceding claims which comprises an exterior coating on top of the solid coating of the Releasable SCC Polymer Composition, for example an exterior coating which comprises one or more coatings of a commercially available flooring finish.
10. A liquid composition comprising (1) an SCC polymer which has an onset of melting temperature, To, of at least 27°C. and a peak melting temperature (Tp) of at most 120°C. and (2) a matrix polymer.
11. A liquid composition according to claim 10 wherein the SCC polymer has one or more of the following characteristics
(a) the SCC polymer has a To of at least 10°C, or at least 15°C, or at least 27°C, or at least 35°C, or at least 40°C,
(b) the SCC polymer has a Tp of at most 80°C, preferably at most 60°C, particularly at most 50°C,
(c) the SCC polymer has a Tp and a T0 , measured in degrees centigrade, such that the value of (Tp - T0) is less than Tp 07, preferably less than 25°C, preferably less than 20°C, particularly less than 15°C,
(d) the SCC polymer has a weight average molecular weight of at most 100,000 Da, preferably at most 50,000 Da, particularly at most 20,000 Da, and in some applications less than 10,000 Da,
(e) the SCC polymer has been prepared by an emulsion
polymerization process which produces particles having a size of 0.07 to
0.5 pm, particularly 0.1 to 0.25 pm, (f) the SCC polymer comprises units derived from one or more n-alkyl acrylates or methacrylates in proportions by weight such that the average length of the n-alkyl groups is 16-20, for example 16-18, carbon atoms, the n-alkyl groups for example containing 8-22 carbon atoms, and the polymer for example containing 90 to 98%, e.g. 94 to 97%, by weight of the units derived from one or more n-alkyl acrylates.
(g) the SCC polymer comprises 90-98%, e.g. 94-97%, by weight of units derived from octadecyl acrylate and hexadecyl acrylate, the ratio of octadecyl acrylate to hexadecyl acrylate units being for example 16 to 2.
(h) the SCC polymer contains, for example in amount greater than 1%, for example 1-4%, e.g. 2-4%, or 1-3%, or 1-2%, units derived from (i) a comonomer containing a carboxylic group, e.g. methacrylic acid, and/or (ii) a comonomer containing a hydroxyl group, e.g. hydroxyethyl acrylate, hydroxyethyl methacrylate hydroxypropyl acrylate or hydroxypropyl methacrylate, and
(i) the SCC polymer has a heat of fusion of at least 20 Joules/g
12. A liquid composition according to claim 11 or 12 wherein the matrix polymer has one or more of the following characteristics: -
(a) the matrix polymer has a minimum film forming temperature
(MFFT) which is at most 20°C,
(b) the matrix polymer has a minimum film forming temperature
(MFFT) which is at least 20X
(c) the matrix polymer is miscible with water,
(d) the matrix polymer is an acrylic or styrene-acrylic polymer prepared by emulsion polymerization, for example a cross-linked styrene- ethylhexylacrylate-methacrylic acid polymer, a styrene-butylacrylate- methacrylic acid polymer, a styrene-butylacrylate-methylmethacrylate- methacrylic acid polymer, or an isobutyl methacrylate-methylmethacrylate- hydroxyethyl acrylate polymer,
(e) the matrix polymer is composed of particles which are smaller than the particles of the SCC polymer, and (f) the matrix polymer forms a continuous phase in which the SCC polymer is dispersed in the form of particles.
PCT/US2016/048878 2015-08-28 2016-08-26 Coated substrates and compositions for coating substrates WO2017040244A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201562211274P 2015-08-28 2015-08-28
US62/211,274 2015-08-28

Publications (1)

Publication Number Publication Date
WO2017040244A1 true WO2017040244A1 (en) 2017-03-09

Family

ID=56997529

Family Applications (2)

Application Number Title Priority Date Filing Date
PCT/US2016/048878 WO2017040244A1 (en) 2015-08-28 2016-08-26 Coated substrates and compositions for coating substrates
PCT/US2016/049117 WO2017040339A1 (en) 2015-08-28 2016-08-26 Coated substrates and compositions for coating substrates

Family Applications After (1)

Application Number Title Priority Date Filing Date
PCT/US2016/049117 WO2017040339A1 (en) 2015-08-28 2016-08-26 Coated substrates and compositions for coating substrates

Country Status (1)

Country Link
WO (2) WO2017040244A1 (en)

Citations (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1125451A (en) * 1965-08-13 1968-08-28 Johnson & Son Inc S C Coating composition
US4830855A (en) 1987-11-13 1989-05-16 Landec Labs, Inc. Temperature-controlled active agent dispenser
US5120349A (en) 1990-12-07 1992-06-09 Landec Labs, Inc. Microcapsule having temperature-dependent permeability profile
US5156911A (en) 1989-05-11 1992-10-20 Landec Labs Inc. Skin-activated temperature-sensitive adhesive assemblies
US5254354A (en) 1990-12-07 1993-10-19 Landec Corporation Food package comprised of polymer with thermally responsive permeability
US5387450A (en) 1989-05-11 1995-02-07 Landec Corporation Temperature-activated adhesive assemblies
US5412035A (en) 1991-02-12 1995-05-02 Landec Corporation Pressure-sensitive adhesives
US5469867A (en) 1992-09-02 1995-11-28 Landec Corporation Cast-in place thermoplastic channel occluder
US5665822A (en) 1991-10-07 1997-09-09 Landec Corporation Thermoplastic Elastomers
US5752926A (en) 1992-04-29 1998-05-19 Landec Corporation Orthopedic casts
WO1999000459A1 (en) 1997-06-26 1999-01-07 S.C. Johnson Commercial Markets, Inc. Improved plasticized aqueous coating compositions
US6199318B1 (en) 1996-12-12 2001-03-13 Landec Corporation Aqueous emulsions of crystalline polymers for coating seeds
US6255367B1 (en) 1995-03-07 2001-07-03 Landec Corporation Polymeric modifying agents
US6376032B1 (en) 1995-05-30 2002-04-23 Landec Corporation Gas-permeable membrane
US6492462B2 (en) 1998-01-16 2002-12-10 Landec Corporation Side chain crystalline polymer as rheology modifier for crosslinked polymer
US6540984B2 (en) 1996-12-12 2003-04-01 Landec Corporation Aqueous dispersions of crystalline polymers and uses
US6544453B2 (en) 1998-01-16 2003-04-08 Landec Corporation Method of using low profile additives for crosslinkable resins
US6831116B2 (en) 1995-03-07 2004-12-14 Landec Corporation Polymeric modifying agents
US6989417B2 (en) 1999-09-17 2006-01-24 Landec Corporation Polymeric thickeners for oil-containing compositions
US7175632B2 (en) 2002-05-15 2007-02-13 Linvatec Corporation Cross-pin graft fixation instruments and method
US7182951B1 (en) 2002-01-29 2007-02-27 Landec Corporation Selection and treatment of seeds
US20070104745A1 (en) * 1996-12-12 2007-05-10 Stewart Ray F Aqueous dispersions of crystalline polymers and uses
US7291389B1 (en) 2003-02-13 2007-11-06 Landec Corporation Article having temperature-dependent shape
WO2010068279A1 (en) * 2008-12-11 2010-06-17 Landec Corporation Thermochromic indicator
US8114883B2 (en) 2007-12-04 2012-02-14 Landec Corporation Polymer formulations for delivery of bioactive materials
WO2012162641A2 (en) 2011-05-25 2012-11-29 Diversey, Inc. Surface coating system and method of making and using same

Patent Citations (34)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1125451A (en) * 1965-08-13 1968-08-28 Johnson & Son Inc S C Coating composition
US4830855A (en) 1987-11-13 1989-05-16 Landec Labs, Inc. Temperature-controlled active agent dispenser
US5156911A (en) 1989-05-11 1992-10-20 Landec Labs Inc. Skin-activated temperature-sensitive adhesive assemblies
US5387450A (en) 1989-05-11 1995-02-07 Landec Corporation Temperature-activated adhesive assemblies
US5783302A (en) 1990-12-07 1998-07-21 Landec Corporation Thermoplastic elastomers
US5120349A (en) 1990-12-07 1992-06-09 Landec Labs, Inc. Microcapsule having temperature-dependent permeability profile
US5254354A (en) 1990-12-07 1993-10-19 Landec Corporation Food package comprised of polymer with thermally responsive permeability
US5412035A (en) 1991-02-12 1995-05-02 Landec Corporation Pressure-sensitive adhesives
US5665822A (en) 1991-10-07 1997-09-09 Landec Corporation Thermoplastic Elastomers
US5752926A (en) 1992-04-29 1998-05-19 Landec Corporation Orthopedic casts
US5807291A (en) 1992-04-29 1998-09-15 Larson; Andrew W. Method of forming an orthopedic cast
US5469867A (en) 1992-09-02 1995-11-28 Landec Corporation Cast-in place thermoplastic channel occluder
US5826584A (en) 1992-09-02 1998-10-27 Schmitt; Edward E. Devices for occluding channels in living mammals
US6255367B1 (en) 1995-03-07 2001-07-03 Landec Corporation Polymeric modifying agents
US6831116B2 (en) 1995-03-07 2004-12-14 Landec Corporation Polymeric modifying agents
US6376032B1 (en) 1995-05-30 2002-04-23 Landec Corporation Gas-permeable membrane
US7169451B2 (en) 1995-05-30 2007-01-30 Landec Corporation Gas-permeable membrane
US6540984B2 (en) 1996-12-12 2003-04-01 Landec Corporation Aqueous dispersions of crystalline polymers and uses
US7175832B2 (en) 1996-12-12 2007-02-13 Landec Corporation Aqueous dispersions of crystalline polymers and uses
US20070104745A1 (en) * 1996-12-12 2007-05-10 Stewart Ray F Aqueous dispersions of crystalline polymers and uses
US6199318B1 (en) 1996-12-12 2001-03-13 Landec Corporation Aqueous emulsions of crystalline polymers for coating seeds
US5977228A (en) 1997-06-26 1999-11-02 S. C. Johnson Commercial Markets, Inc. Plasticized aqueous coating compositions
WO1999000459A1 (en) 1997-06-26 1999-01-07 S.C. Johnson Commercial Markets, Inc. Improved plasticized aqueous coating compositions
US6544453B2 (en) 1998-01-16 2003-04-08 Landec Corporation Method of using low profile additives for crosslinkable resins
US6492462B2 (en) 1998-01-16 2002-12-10 Landec Corporation Side chain crystalline polymer as rheology modifier for crosslinked polymer
US7449511B2 (en) 1999-09-17 2008-11-11 Landec Corp. Polymeric thickeners for oil-containing compositions
US7101928B1 (en) 1999-09-17 2006-09-05 Landec Corporation Polymeric thickeners for oil-containing compositions
US6989417B2 (en) 1999-09-17 2006-01-24 Landec Corporation Polymeric thickeners for oil-containing compositions
US7182951B1 (en) 2002-01-29 2007-02-27 Landec Corporation Selection and treatment of seeds
US7175632B2 (en) 2002-05-15 2007-02-13 Linvatec Corporation Cross-pin graft fixation instruments and method
US7291389B1 (en) 2003-02-13 2007-11-06 Landec Corporation Article having temperature-dependent shape
US8114883B2 (en) 2007-12-04 2012-02-14 Landec Corporation Polymer formulations for delivery of bioactive materials
WO2010068279A1 (en) * 2008-12-11 2010-06-17 Landec Corporation Thermochromic indicator
WO2012162641A2 (en) 2011-05-25 2012-11-29 Diversey, Inc. Surface coating system and method of making and using same

Non-Patent Citations (9)

* Cited by examiner, † Cited by third party
Title
J. POLY. SCI, (POLYMER CHEMISTRY, vol. 7, 1969, pages 3053
J. POLY. SCI, MACROMOL. REV, vol. 8, 1974, pages 117
J. POLY. SCI, POLY-PHYSICS ED, vol. 18, 1980, pages 2197
J. POLY. SCI., vol. 60, 1962, pages 19
JACS, vol. 75, 1953, pages 3326
JACS, vol. 76, pages 6280
MACROMOLECULES, vol. 12, 1979, pages 94
POLY. SCI USSR, vol. 21, 1979, pages 241
POLYMER J, vol. 17, 1985, pages 991

Also Published As

Publication number Publication date
WO2017040339A1 (en) 2017-03-09

Similar Documents

Publication Publication Date Title
EP1008635B1 (en) Dirt pickup resistant coating binder and coatings
CN104204007B (en) Polymer, method and composition
TWI373501B (en) Aqueous floor polishing composition
US9000069B1 (en) Self-stratifying coatings
NZ243386A (en) Elastomeric compositions comprising two incompatible polymers and a photosensitive compound or composition
JP7100456B2 (en) Modified polyolefin resin
CN108026405B (en) Resin emulsion for paint
WO2016179076A1 (en) Acrylic emulsion adhesives
CN102351979A (en) Acrylic resin coating liquid for alumite coloring layer and preparation method thereof
EP1371705A1 (en) Water-based adhesives
CN107406557B (en) Aqueous polymer emulsion
MXPA04005377A (en) Aqueous copolymer composition and method for preparing a coating therefrom.
US20170058143A1 (en) Coated Substrates and Compositions for Coating Substrates
CN1289787A (en) Polymers as coating materials
EP3472250B1 (en) Coating composition with improved liquid stain repellency
CN110536947B (en) Multimodal polymer composition
WO2017040244A1 (en) Coated substrates and compositions for coating substrates
TWI826368B (en) Water-based pressure sensitive adhesive compositions and methods of making same
JP5199922B2 (en) Multi-layer coating formation method
JP3525593B2 (en) Aqueous nail polish
EP3283569B1 (en) Aqueous dispersion and uses thereof
TWI275620B (en) Topcoat coating composition
JP7352810B2 (en) Fluorine-containing polymer, coating composition, method for producing coated articles, and coated articles
JP4683515B2 (en) Formation method of multilayer coating film
EP2855539A1 (en) Pressure-sensitive adhesives comprising low molecular weight acid-functional acrylic resins and methods of making and using same

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 16770810

Country of ref document: EP

Kind code of ref document: A1

NENP Non-entry into the national phase

Ref country code: DE

122 Ep: pct application non-entry in european phase

Ref document number: 16770810

Country of ref document: EP

Kind code of ref document: A1